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RADI LARIA<br />
VOLUME 14 MAY 1994<br />
NEWSLETTER OF THE<br />
INTERNATIONAL ASSOCIATION OF RADIOLARIAN PALEONTOLOGISTS<br />
ISSN: 0297.5270
President<br />
AKIRA YAO<br />
Osaka, JAPAN<br />
INTERRAD<br />
International Association of Radiolarian Paleontologists<br />
Editor<br />
LUIS O'DOGHERTY<br />
Institut de Géologie et Paléontologie<br />
BFSH-2 Université de Lausanne<br />
CH-1015, SWITZERLAND<br />
Tel: (41) 21-6924360 Fax: (41) 21-6924305<br />
E-mail: Lodogher@igp.unil.ch<br />
Paleozoic<br />
JONATHAN AITCHISON Sydney, AUSTRALIA<br />
Mesozoic<br />
PATRICK DE WEVER Paris, FRANCE<br />
OFFICERS OF THE ASSOCIATION<br />
Secretary<br />
PETER O. BAUMGARTNER<br />
Lausanne, SWITZERLAND<br />
Working Group Chairmen<br />
Secretary - Interrad VII Osaka<br />
ATSUSHI TAKEMURA<br />
Geoscience Institute Hygoyo University of Teacher Education<br />
942-1 Shimokume; Yashiro-cho, Kato-gun<br />
673-14 Hyogo, JAPAN<br />
Tel: (81) 795-44-2206 Fax: (81) 795-44-2189<br />
Past President<br />
MARTA MARCUCCI-PASSERINI<br />
Florence, ITALY<br />
Treasurer<br />
JEAN-PIERRE CAULET<br />
Muséum National d’Histoire Naturelle<br />
Laboratoire de Géologie. 43, rue Buffon<br />
75005 Paris, FRANCE<br />
Tel: (33) 1-40793471 or 59 Fax: (33) 1-40793739<br />
E-mail: caulet@cimrs1.mnhn.fr<br />
Cenozoic<br />
ANNIKA SANFILIPPO California, U.S.A.<br />
Recent<br />
DEMETRIO BOLTOVSKOY Buenos Aires, ARGENTINA<br />
INTERRAD is an international non-profit organization for researchers interested in all aspects of<br />
<strong>radiolaria</strong>n taxonomy, palaeobiology, morphology, biostratigraphy, biology, ecology and paleoecology.<br />
INTERRAD is a Research Group of the International Paleontological Association (IPA). Since 1978<br />
members of INTERRAD meet every three years to present papers and exchange ideas and materials<br />
INTERRAD MEMBERSHIP: The international Association of Radiolarian Paleontologists is open to any<br />
one interested on receipt of subscription. The actual fee US $ 15 per year. Membership queries and<br />
subscription send to Treasure. Changes of address send to the Editor.<br />
BIBLIOGRAPHIES: The bibliographies are produced by the Editor. Any suggestion, reprints of articles and<br />
details of omission should be sent to him directly. Please send reprints of any <strong>radiolaria</strong>n article to the<br />
Editor this facilitate the edition of forthcoming bibliographies.
RADIOLARIA<br />
Newsletter of the International Association of Radiolarian Paleontologists<br />
VOLUME 14 MAY 1994<br />
Edited by: Luis O'Dogherty<br />
Institut de Géologie et Paléontologie; BFSH-2, Université de Lausanne<br />
CH-1015 Switzerland<br />
CONTENTS<br />
Editorial .................................................................................................................................................................................................<br />
Letter from the Secretary ........................................................................................................................................................... 3<br />
Forum: ....................................................................................................................................................................................................<br />
4<br />
Paulian Dumitrica ................................................................................................................................................................... 4<br />
Demetrio Boltovskoy ............................................................................................................................................................ 4<br />
News: ........................................................................................................................................................................................................<br />
Radiolarian research in New Zealand. Chris Hollis .................................................................................... 5<br />
Micropaleontological Reference Centers. Annika Sanfilippo .............................................................. 6<br />
Nazarov's collection. Andreas Braun ..................................................................................................................... 8<br />
Jurassic-Cretaceous Working Group. Peter O. Baumgartner .................................................................. 8<br />
Cenozoic Working Groups. Catherine Nigrini & Annika Sanfilippo ................................................... 9<br />
Paleozoic Working Groups. Jonathan C. Aitchison ................................................................................. 10<br />
News from the International Paleontological Association. .................................................................. 11<br />
Ocean Drilling Program News. ............................................................................................................................... 12<br />
Symposia .............................................................................................................................................................................................<br />
"Radiolarian events" Symposium I. G C. Kyoto, 1992. Akira Yao ................................................ 13<br />
Radiolarian Symposium Moscow, 1993. Spela Gorican and Valentina S. Vishnevskaya ......... 14<br />
Electronic Mail Directory. Demetrio Boltovskoy and Luis O'Dogherty .............................................................. 16<br />
Interrad VII, Osaka; 2nd Circular. Atsushi Takemura ............................................................................................ 16<br />
New Announcement of Interrad VII. Atsushi Takemura .................................................................................... 20<br />
International Meetings. .............................................................................................................................................................. 21<br />
Bibliography 1989-1994. Luis O'Dogherty ................................................................................................................ 23<br />
Announcements ...........................................................................................................................................................................<br />
Japanese Publications. Yosiaki Aita ................................................................................................................ 108<br />
Calendar of Radiolaria. Paula Noble and Donna Hull ............................................................................... 108<br />
RadRefs. Annika Sanfilippo, Nona Renz, Caty Nigrini and Jean-Pierre Caulet ................................ 109<br />
Biochronological Correlations. Jean Guex ................................................................................................... 109<br />
Address Directory. Luis O'Dogherty ............................................................................................................................. 110<br />
Announcements. Jurassic-Cretaceous Working Group ............................................................................................ 124<br />
Financial support by<br />
Institut de Géologie. Université de Lausanne. Switzerland<br />
2<br />
5<br />
13<br />
108
Editorial Radiolaria 14<br />
Frequently, in French a person working for<br />
free, is classified as a "worker for the King of<br />
Prussia". There is again another crazy team<br />
working for our beloved King. The king gets as a<br />
result, this new edition of Radiolaria. We are aware<br />
of the fact that quite a few years have passed since<br />
Patrick De Wever has decided to leave the<br />
responsibility of edition. We have taken the risk of<br />
covering four years of absence with only a single<br />
issue. Nevertheless, we hope that this new issue will<br />
recover the lack of information accumulated since<br />
Radiolaria 13.<br />
Sixteen years ago, when our friend Patrick<br />
began with "Eurorad-News" (the direct ancestor of<br />
Radiolaria), the principal purpose of his work was<br />
a bulletin of liaison and information among<br />
<strong>radiolaria</strong>n researcher. Patrick had been regularly<br />
working through all these years, and the newsletter<br />
offered news, reports, bibliographical references,<br />
addresses, forums, discussions, etc.; in other words<br />
a wonderful media where there was place for<br />
everybody and everything. It was only during the<br />
preparation of this issue of Radiolaria that we<br />
realized how hard a job it is! We are, however<br />
determined to continue in Patrick's footsteps.<br />
This issue has been sent to INTERRAD<br />
members only 106 person. All the other person<br />
EDITORIAL<br />
Working again for the King of Prussia<br />
- 2 -<br />
in our address list received an announcement and<br />
an invitation to join INTERRAD and receive<br />
Radiolaria. Our objective are two fold: firstly, to<br />
show that Radiolaria is still alive, second and the<br />
most important, to try to get new members.<br />
This is a newsletter to and for everybody, so<br />
we would appreciate your comments. Included in<br />
this newsletter you will find a postcard, please<br />
complete it and send it back to us. This is to<br />
acknowledge the receipt of this issue and to help<br />
us to update our address directory.<br />
With this volume, a new generation of<br />
Radiolaria has started. We hope that this work will<br />
be as good as Patrick's.<br />
Finally, we would wish to dedicate this issue to<br />
our friend Patrick in honour of his generous work<br />
for the community of <strong>radiolaria</strong>n researcher. Only<br />
God knows the hours that Patrick spent through<br />
all these years for the King!. Thanks, Patrick, for<br />
having offered us thirteen unforgettable volumes.<br />
Luis O'Dogherty
Radiolaria 14 Secretary's Letter<br />
Five years have passed since the last issue,<br />
RADIOLARIA 13. Five years of almost explosive<br />
activity in all fields of research dealing with<br />
Radiolaria. When I was elected secretary in 1991,<br />
during INTERRAD VI, Florence, I promised to<br />
produce RADIOLARIA 14 in 1992. However, this<br />
work was delayed by several circumstances. One<br />
of them was, that most of my time dedicated to<br />
<strong>radiolaria</strong>n research was tied up with the<br />
preparation of the Jurassic-Cretaceous Atlas (see<br />
announcement on inside of back cover). Another<br />
was, that my collaborators were busy finishing<br />
their thesis and could not spear time for<br />
RADIOLARIA. A third was my eye illness that<br />
caused months of incapacity for office work in<br />
1993, but is stabilized since.<br />
Now, Spela Gorican, Ruth Jud and Luis<br />
O'Dogherty, have finished their thesis and I would<br />
like to congratulate them for their excellent work<br />
and thank them for their collaboration during the<br />
past years. Since, Luis has taken the entire<br />
production of RADIOLARIA 14 in his hands. The<br />
result is the volume that you just opened. It<br />
represents certainly the most complete<br />
bibliography on Radiolaria of the last five years. I<br />
am thankful to Luis for his work and wish that he<br />
would find time in the future to continue what he<br />
started.<br />
Besides the regular production of<br />
RADIOLARIA on paper, we would like to<br />
promote databases that contain the same<br />
Letter from the Secretary of Interrad<br />
- 3 -<br />
information in searchable form. Perhaps next year<br />
we can offer you RADIOLARIA on diskette...<br />
However, we do not want to compete with<br />
"RADREFLIB" by A. Sanfilippo and others (see<br />
announcement p. 107). Annika and her<br />
colleagues are doing excellent work that has<br />
helped us much through all the past years.<br />
However, even the best bibliography can be<br />
improved. One of the bases for such improvement<br />
is the knowledge of the latest references on<br />
<strong>radiolaria</strong>n work. It depends on your contribution.<br />
Please, send reprints of your recent publications,<br />
or of any publication that has never been reported<br />
in RADIOLARIA.<br />
At last, I would like to thank all contributors to<br />
this issue for their effort to make it lively and upto-date.<br />
RADIOLARIA is as good as you want it<br />
to be. RADIOLARIA is depending on your<br />
informations, progress reports, opinions,<br />
discussions ....<br />
I would like thank you all for your patience<br />
and fidelity and hope to see you at INTERRAD<br />
VII, Osaka for another exciting meeting on<br />
Radiolaria.<br />
Yours sincerely,<br />
Peter O. Baumgartner
Forum Radiolaria 14<br />
Dear <strong>radiolaria</strong>n colleagues:<br />
After so many years here is another issue of<br />
RADIOLARIA. Thanks to Luis O'Dogherty who after the<br />
presentation of his thesis devoted almost two month of<br />
his precious time to gather up all the literature published<br />
since 1989 or even a little earlier, and to write to our<br />
colleagues settled in all the four cardinal points, we have<br />
again a journal to lend a hand to international cooperation<br />
among <strong>radiolaria</strong>n workers. I think that we all have felt its<br />
absence.<br />
The first series of this journal, successfully edited by<br />
our colleague Patrick De Wever, died in 1989, an ill-fated<br />
year for the communist regimes, with its volume 13,<br />
again an ill-fated number. Patrick was at pains of doing<br />
the best of it and we have to admit that he succeeded in<br />
doing from his RADIOLARIA both an informative<br />
journal on our current activities, addresses, bibliography,<br />
and a forum where we could exchange ideas and thoughts,<br />
and debate controversial aspects of <strong>radiolaria</strong>n research. Let<br />
us hope that this new series will be at least at the same<br />
level and that it will go on again for at least other 13<br />
volumes. Again 13?<br />
In all these years the <strong>radiolaria</strong>n bibliography has<br />
enriched with many titles, I don't know exactly how<br />
many, but the list of papers my friend Luis has tried to<br />
draw up is possible to approximate rather exactly their<br />
number. These articles regard a large field of aspects of<br />
<strong>radiolaria</strong>n research, from systematics, morphology,<br />
ontogeny, evolution, biostratigraphy, paleogeography, to<br />
diagenesis of <strong>radiolaria</strong>n skeletons, sedimentology and<br />
origin of <strong>radiolaria</strong>n-bearing rocks, etc., so that it is<br />
almost impossible at present to become well acquainted<br />
with all that is published on Radiolaria. At the same time<br />
the use of the SEM in <strong>radiolaria</strong>n study and illustration,<br />
especially for the Mesozoic and Paleozoic species has<br />
generalized, and of the computer in the interpretation of<br />
<strong>radiolaria</strong>n data has rapidly increased.<br />
All these have allowed us to better know this group<br />
of protists. Unfortunately this increase in the number of<br />
papers has not always resulted in a similar increase in<br />
knowledge of <strong>radiolaria</strong>ns. A number of species and genera<br />
has been too briefly defined, without an adequate<br />
illustration or knowledge of skeletal morphology. In their<br />
rush at new names or priorities some authors, fortunately<br />
Dreams and realities in Paleontology<br />
Paulian Dumitrica<br />
- 4 -<br />
not too many, have forgotten that the description of a new<br />
taxon implies much responsibility from their part. In<br />
some cases the illustrations are so poor that it is<br />
impossible to recognize the species ''figured''. One forgets<br />
that a good illustration is worthier than many pages of<br />
description. One forgets also that homoeomorphy is<br />
frequent among <strong>radiolaria</strong>ns and especially among<br />
spumellarians and entactinarians. That is why for the<br />
description of new taxa of such <strong>radiolaria</strong>ns it is<br />
necessary, in many cases, to know the internal<br />
morphology. Practice has proven that the effort deposed<br />
for the subsequent recognition of a taxon is inversely<br />
proportional to the effort deposed for its initial<br />
description. Or as a Rumanian proverb says: somebody<br />
throws a stone into the water and ten madmen plunge to<br />
find it.<br />
I appeal also to the colleagues who publish their new<br />
taxa in other languages than English, French, German,<br />
Italian or Latin to observe the recommendations of the<br />
ICZN (Appendix E 4, 5) and to accompany their<br />
description and explanations of figures by a translation<br />
into one of these languages. In writing this I think not<br />
only of some Russian colleagues but also, and especially,<br />
of some Chinese ones. It is true that these two languages<br />
are spoken or known by hundreds of millions or, in the<br />
latter case, by more than a billion of peoples but we have<br />
to observe the Recommendations of the Code. It is the<br />
only way to understand each other and to use the results of<br />
our research.<br />
Finally I appeal to another Recommendation of the<br />
ICZN: Appendix A (Code of ethics). Sometimes it is<br />
forgotten. I think that it is not recommendable to publish<br />
a new name for a taxon (be it species or genus) described<br />
in still unpublished dissertations in the case we are aware<br />
of it. This should be especially the case when such a<br />
taxon has already been used by other authors. One could<br />
simply publish the original name and diagnosis under the<br />
original authorship in order to make the name valid<br />
according to Articles 9 and 11 of ICZN.<br />
With this I wish everybody a fruitful year and the<br />
chance to participate to the InterRad VII<br />
On the waning relevance of bug-based work in paleoceanography<br />
Are faunal/floral approaches to stratigraphicpaleoceanographic<br />
surveys an extinguishing species? I<br />
thought at first that this feeling was only my biased<br />
appreciation of the situation, but talking to people and<br />
scanning through presentations during the last few years'<br />
meetings reinforced my feeling that, in effect, fewer and<br />
Demetrio Boltovskoy<br />
Paulian Dumitrica<br />
fewer people make slides and look at the bugs Moreover,<br />
many of the few that used to identify species are<br />
switching to putting shells in vials and running chemical<br />
analyse on them. Carbon and, specially, oxygen isotopes<br />
are THE DATA that use up to 70-80% of the poster space<br />
and oral presentation time in todays congresses.
Radiolaria 14 News<br />
Usefulness of this information, fast acquisition of<br />
impressive numbers of data points, ease of comparison<br />
with literature data, are some of the advantages that made<br />
isotope studies so popular. I think, however, that one of<br />
the major factors that contributed to the decline in the<br />
interest for surveys based on species identifications is our<br />
inability to work out a common language as far as the<br />
names and shapes of the bugs we deal with are concerned.<br />
Some years ago, we (Boltovskoy & Jankilevich)<br />
compared the results of our rad identifications in a small<br />
plankton collection from the equatorial Pacific ocean with<br />
publications based on materials that undoubtedly exceeded<br />
our coverage several-fold [Oceanologica Acta, 8:101-123,<br />
1985]. Only Petrushevskaya's reports seemed to include<br />
all the species that we found, while the remaining 8<br />
studies analyzed reported 88% to as little as 18% of our<br />
taxa. I have very little doubt that the missing <strong>radiolaria</strong>ns<br />
were present in their collections: they were either ignored,<br />
or lumped with other forms, or split to the point one<br />
cannot trace equivalencies. I am not implying that we<br />
were right and all the others were wrong, but just<br />
pointing out that we did not communicate. There<br />
obviously was a language problem.<br />
When looking at the illustration of a "new" species<br />
just published in the literature, didn't you sometime have<br />
the "deja vue" feeling? Well, I've had it quite often, and<br />
sometimes, just for fun, I'd go to Haeckel or Popofsky or<br />
some other old monograph... and there it is! with horns,<br />
spines, and everything! Creating a "new" taxon is much<br />
much easier than combing all the dusty books in search of<br />
an adequate name for the odd shell one comes across in the<br />
slide. And since too few reviewers seem to care much the<br />
new name makes its way into print and contributes its<br />
sand grain to the already hectic mess.<br />
Unfortunately, the process of erecting new names has<br />
practically no rules to it. One just sends the manuscript;<br />
if it is lucky enough as to be reviewed by someone who<br />
cares little about nomenclature and systematics, the paper<br />
gets published and the new names are formally valid<br />
thereafter.<br />
Is there anything that can be done to mitigate this<br />
problem? In my opinion - yes. Good identifications are<br />
§A welcome spin-off from Yoshiaki Aita's sojourn here<br />
as a post-doctoral fellow at Auckland University has been<br />
a rapid rise in interest in using Mdiolarians to improve<br />
age control in poorly dated Mesozoic basement rocks and<br />
Cretaceo-Paleogene limestones.<br />
Geologists from the Institute of Geological and<br />
Nuclear Sciences aGNS, ex DSIR Geology and<br />
Geophysics, formerly NZ Geological Survey!) are<br />
successfully retrieving Triassic and Jurassic <strong>radiolaria</strong>ns<br />
from cherts and phosphate nodules in the greywackes<br />
around Wellington.<br />
Radiolarian research in New Zealand<br />
Chris Hollis<br />
- 5 -<br />
obviously the starting point, but then we all think that<br />
our own identifications are good. But what about other<br />
people's identifications? Yes, we can definitely criticize<br />
those, or at least some of them. Look, for example, at<br />
Paulian Dumitrica's approach at describing new taxa (e.g.,<br />
Revista Española de Micropaleontología, 21:207-264,<br />
1989); I doubt that any of us would dare to question his<br />
work. Each new species is illustrated in photographs, line<br />
drawings, thin-sections, thoroughly described and<br />
compared with related morphotypes. And then check other<br />
descriptions of new taxa (no, I won't give examples: we<br />
all have some good examples to offer anyway...).<br />
I have the feeling that avoiding spurious new species<br />
is as much a responsibility of the author, as it is of the<br />
referees and of the editors. When acting as referees, we<br />
should probably require some minimum standards for<br />
accepting a new species from a colleague. These minima<br />
should take into account the number of specimens used<br />
(measured, photographed, thin-sectioned) for the erection<br />
of the new taxon, the literature checked in search of<br />
synonyms, the variability within the taxon and<br />
similarities with other species, etc., etc.<br />
This problem is not a recent one: Ernst Haeckel, in<br />
his 1887 (Challenger) monograph, included 3389<br />
<strong>radiolaria</strong>n species, 2785 of which were described as new.<br />
Nowadays we are all aware of the fact that quite a few of<br />
these taxa are synonyms, but at the turn of the century<br />
there were no isotopes to compete with. Cathy Nigrini<br />
and Ted Moore's 1979 <strong>radiolaria</strong>n guide (A guide to<br />
Modern Radiolaria, Cushman Foundation for<br />
Foraminiferal Research, Special Publication 16) was a<br />
cornerstone that did a lot for improving our<br />
communication as far as <strong>radiolaria</strong>n names and shapes are<br />
concerned. But the decade elapsed since that work requires<br />
a new similar effort to put some order in <strong>radiolaria</strong>n<br />
taxonomy. A Nigrini-Petrushevskaya-Dumitrica (as a<br />
biologist I am restricting my scope to Cenozoic<br />
<strong>radiolaria</strong>ns) coauthored updated guide would be an epochmaking<br />
update.<br />
Demetrio Boltovskoy<br />
Barry O'Connor, a graduate student at Auckland<br />
University, has obtained rich mid-to Late-Oligocene (with<br />
some Eocene) faunas from the poorly dated Mahurangi<br />
Limestone north of Auckland. His excellent TM and SEM<br />
photos will be a valuable record of these very well<br />
preserved southem mid-latitude faunas.<br />
Although mainly working on Recent benthic<br />
foraminifera at present, Chris Hollis is managing to find<br />
some time for extending his studies of Cretaceo-Paleogene<br />
<strong>radiolaria</strong>ns from the Amuri Limestone in Marlborougll<br />
(NE South Isla~ld), including biostratigraphic study of<br />
<strong>radiolaria</strong>ns and foraminifera (with Percy Strong of IGNS)
News Radiolaria 14<br />
from a Late-Cretaceous to Middle-Eocene siliceous<br />
limestone sequence in inland Marlborough, and<br />
combining geochemical data with his microfossil results<br />
to strengthen the evidence for a prolonged cool episode at<br />
the base of the Paleocene (with geochemists at Auckland<br />
University). Chris has also obtained a JSPS fellowship to<br />
join Yoshiaki Aita and Prof. Toyosaburo Sakai at<br />
The Deep Sea Drilling Project (DSDP), predecessor<br />
of the Ocean Drilling Program (ODP) which JOI (Joint<br />
Oceanographic Institutions, Inc.) currently manages,<br />
produced an enormous wealth of new biostratigraphic<br />
information from its 96 legs. As ODP continues to gather<br />
data from all over the world it becomes increasingly<br />
important to establish and maintain Micropaleontological<br />
Reference Centers housing representative preparations of<br />
DSDP/ODP microfaunas and -floras to serve the<br />
international community of biostratigraphers. Four<br />
centers are located in the U.S. - Lamont-Doherty<br />
Geological Observatory, U.S. National Museum of<br />
Natural History, Texas A&M University and Scripps<br />
Institution of Oceanography. The other Centers are located<br />
in Western Europe (Basel), USSR (Moscow), Japan<br />
(Tokyo) and New Zealand (Lower Hutt). The published<br />
Initial Reports contain contributions on the microfaunas<br />
and floras, recorded by the shipboard and shorelab parties<br />
and these include many new species descriptions. Core<br />
material is by no means inexhaustible and therefore access<br />
to it has to be restricted to requests for research material<br />
leading to publication. Even so, important material is<br />
sampled out of existence. The aim for the centers is thus:<br />
1. Preserve material from important levels for all time.<br />
2. Make it possible for researchers to see the quality of<br />
preservation and the composition of a large number of<br />
microfaunas and floras and, therefore, plan their own<br />
sample requests in the most advantageous way.<br />
3. Allow scientists to compare actual prepared faunas and<br />
floras (equivalent to type material) with published figures<br />
and descriptions in the literature.<br />
4. Provide reference collections at geographically<br />
widespread localities, enabling individual researchers to<br />
reach them easily and with a minimum of traveling cost.<br />
5. Provide the above facility for scientists working on<br />
Foraminifera, Calcareous nannofossils, Radiolaria and<br />
Diatoms.<br />
Funding to prepare the <strong>radiolaria</strong>n slides became<br />
available through JOI in October 1990. Annika<br />
Sanfilippo and Amy Weinheimer have to date prepared and<br />
distributed 2600 Tertiary samples from DSDP Legs 1-96.<br />
The samples were originally selected to give the best<br />
representation possible for each leg, approximately one<br />
sample per core, or one on either side of a zonal boundary.<br />
Foraminifera preparations are also complete for DSDP<br />
Micropaleontological Reference Centers<br />
Ocean Drilling Program - Deep Sea Drilling Project<br />
Annika Sanfilippo<br />
- 6 -<br />
Utsunomiya University for a year to work on<br />
comparisons between southem and northem mid-latitude<br />
Cretaceo-Paleogene <strong>radiolaria</strong>ns, with an emphasis on<br />
biostratigraphy, evolution and the K-T transition.<br />
Chris Hollis<br />
Legs 1-96, and diatom and nannofossil preparations have<br />
so far been made for approximately half of the legs.<br />
Funding is presently being requested to continue<br />
preparation of <strong>radiolaria</strong>n slides for the ODP legs.<br />
Fossil Material<br />
Located at eight sites around the world, the<br />
Micropaleontological Reference Centers provide scientists<br />
with an opportunity to examine microfossils of various<br />
geologic ages and provenance. The collections cover four<br />
microfossil groups-calcareous nannofossils, foraminifers,<br />
<strong>radiolaria</strong>ns, and diatoms-selected from sediment cores<br />
obtained from the Deep Sea Drilling Project (DSDP) and<br />
its successor, the Ocean Drilling Program (ODP).<br />
Material has so far been chosen from Legs 1 through 128,<br />
with each Center carrying identical sample sets. The<br />
organization has been supervised by John Saunders of the<br />
Western Europe Center and William Riedel of the U.S.<br />
West Coast facility under the mandate of the JOIDES<br />
Information Handling Panel.<br />
All fossil material maintained by the Reference<br />
Centers remains the property of the U.S. National Science<br />
Foundation and is held by the Centers on semipermanent<br />
loan.<br />
Ocean Drilling Program<br />
During its more than 7 years of seagoing operations,<br />
the Ocean Drilling Program (ODP), operating the drilling<br />
vessel JOIDES Resolution, has cored almost 70,000<br />
meters of deep-sea sediment. Like its predecessor, the<br />
Deep Sea Drilling Project (DSDP), which operated the<br />
drilling vesssel Glomar Challenger from 1968 to 1983,<br />
ODP has recovered cores from the Atlantic, Pacific,<br />
Indian, and Southern Oceans and the Mediterranean and<br />
Norwegian-Greenland Seas.<br />
ODP is based in College Station, Texas, where Texas<br />
A&M University serves as Science Operator for the<br />
Program. Texas A&M provides administrative, staffing,<br />
and technical support for the JOIDES Resolution. Overall<br />
scientific planning and program advice are provided by an<br />
international scientific organisation, the Joint<br />
Oceanographic Institutions for Deep Earth Sampling<br />
(JOIDES). Members of JOIDES panels and committees<br />
represent the United States, the Canada and Australia<br />
Consortium for Ocean Drilling, the Federal Republic of<br />
Germany, France, Japan, the United Kingdom,
Radiolaria 14 News<br />
U.S.S.R.,* and the European Science Foundation<br />
Consortium for Ocean Drilling. Yearly membership<br />
contributions from each of these sources fund the<br />
operations of the Program.<br />
(*As of December 1991)<br />
Purpose<br />
Since 1968 the Glomar Challenger and her successor,<br />
the JOIDES Resolution, have recovered sediment cores<br />
from all the major ocean basins. This wealth of deep-sea<br />
material is providing scientists with important<br />
information on global history and giving paleontologists<br />
a great amount of new biostratigraphic data. Because<br />
critical levels from the cores will eventually be sampled<br />
out of existence, it is the primary goal of the Centers to<br />
preserve such prime reference material for both present and<br />
future investigators.<br />
At the eight Centers, the reference collections enable<br />
researchers to compare prepared material with the reports<br />
and illustrations published in DSDP Initial Reports and<br />
ODP Proceedings volumes. This will help to stabilize<br />
taxonomy and the review of biostratigraphic and<br />
paleoenvironmental problems. In addition, it enables<br />
1 U.S. West Coast<br />
Scripps Institution of Oceanography<br />
La Jolla, CA 92093<br />
Supervisor: Dr. Annika Sanfilippo<br />
Telephone: 619-534-2049<br />
Telex: 910337127 IUC WWD SIOSDG<br />
Fax: 619-534-0784<br />
2 U.S. Gulf Coast<br />
Texas A&M University<br />
Department of Oceanography<br />
College Station, TX 77843-3146<br />
Supervisor: Dr. Stefan Gartner<br />
Telephone: 409-845-8479 or -7211<br />
Fax: 409-845-6331<br />
3 U.S. National Museum<br />
U.S. Museum of Natural History<br />
Department of Paleobiology<br />
Smithsonian Institution<br />
Washington, DC 20560<br />
Supervisor: Dr. Brian Huber<br />
Telephone: 202-786-2668<br />
Telex: 264729<br />
Fax: 202-357-4779<br />
4 U.S. East Coast<br />
Lamont-Doherty Geological Observatory<br />
Palisades, NY 10964<br />
Supervisor: Ms. Rusty Lotti<br />
Telephone: 914-359-2900<br />
Fax: 914-365-2312<br />
- 7 -<br />
requests to ODP for core material to be planned with<br />
greater precision.<br />
Facilitites<br />
Reference Center Locations<br />
All of the Centers maintain identical sets of<br />
microfossil preparations. Listed are materials and<br />
equipment available for visitor use:<br />
• secure storage and display areas<br />
• binocular microscopes and work space<br />
• more than 4000 nannofossil and foraminiferal<br />
preparations; more than 3000 <strong>radiolaria</strong>n and 800 diatom<br />
preparations<br />
• lithologic smear slides for each fossil sample<br />
• computer listings of samples<br />
• information on CD-ROMs for Legs 1 through 129<br />
• sets of DSDP Initial Reports and ODP Proceedings<br />
For more information about any Reference Center, or<br />
to schedule a visit, contact the Supervisor at the location.<br />
5 Western Europe<br />
Natural History Museum<br />
CH-4001 Basel, Switzerland<br />
Supervisor: Mr. John Saunders<br />
Telephone: 41-61-266-5564<br />
Fax: 41-61-266-5546<br />
6 Russia<br />
Institute of the Lithosphere<br />
Academy of Sciences<br />
Staromonetny Pereylok, 22<br />
Moscow 109180, Russia<br />
Supervisor: Dr. Ivan Basov<br />
Telephone: 71-095-231-4836<br />
Fax: 71-095-233-5590<br />
7 Japan<br />
National Science Museum<br />
Department of Geology<br />
3-23-1 Hyakunin-cho Shinjuku-ku<br />
Tokyo, 160, Japan<br />
Supervisor: Dr. Y. Tanimura<br />
Telephone: 81-33-364-2311<br />
Fax: 81-33-364-2316<br />
8 New Zealand<br />
New Zealand Geological Survey<br />
P.O. Box 30368<br />
Lower Hutt, New Zealand<br />
Supervisor: Dr. C.P. Strong<br />
Telephone: 64-4-569-9059<br />
Fax: 64-4-569-5016<br />
Annika Sanfilippo
News Radiolaria 14<br />
Inspection of the <strong>radiolaria</strong>n collection of Dr. Boris B. Nazarov in the Geological Institute of the<br />
Academy of Sciences in Moscow.<br />
Not only those working with on Paleozoic<br />
<strong>radiolaria</strong>ns of various ages will be well aware of the<br />
fundamental works of Dr. B. Nazarov on this group.<br />
Unfortunately many of the species he described have been<br />
documented by only inadequately printed photographs, so<br />
that better documentation of this material is one of the<br />
main purpose preceding future taxonomic work. Thanks<br />
to the help of Dr. V.S. Vishnevskaya (Institute of<br />
Lithosphere of the Academy of Science, Moscow) and Dr.<br />
I. Khokhlova (Geological Institute of the Academy of<br />
Science, Moscow), a visit and inspection of this<br />
important collection has been made possible by the<br />
representatives of the Geological Institute.<br />
You may already have noticed the announcement of<br />
our long-expected Jurassic Cretaceous <strong>radiolaria</strong>n Atlas on<br />
the inside of the back cover of this issue. Yes, it will be<br />
published this year. In the following, I would like to<br />
report on the state of the work and especially on the<br />
philosophy and the working compromises that we adopted<br />
during the past five years of execution of this project.<br />
Our Working Group (WG) has held three meetings<br />
(Lausanne 1989, Munich 1990, Paris 1991). During these<br />
meetings we discussed about 600 taxa one by one and<br />
came to an agreement on the systematics. The taxa to be<br />
used for the creation of a Middle Jurassic to Lower<br />
Cretaceous <strong>radiolaria</strong>n biozonation were selected from the<br />
material provided by the members of the WG. Taxa<br />
difficult to identify in poorly preserved material have<br />
preferentially been placed at subspecies level, whereas our<br />
species level represents more broadly defined groups of<br />
morphotypes determinable even in poorly preserved<br />
samples.<br />
Obviously, this effort of grouping was the most<br />
difficult task for which we spent most of the discussion<br />
time. The grouping, based on the material known to the<br />
WG-members, was, however, absolutely necessary to<br />
achieve correlation between samples with a wide range of<br />
preservational stages, typical for Mesozoic <strong>radiolaria</strong>ns.<br />
During preliminary data treatment for the zonation (see<br />
below) some drawbacks of our grouping effort appeared.<br />
First, it was expected that our species would turn out with<br />
longer ranges than our subspecies. This could be<br />
confirmed. However, in many cases we lost some of the<br />
Andreas Braun<br />
Jurassic-Cretaceous Working Group<br />
Peter O. Baumgartner<br />
- 8 -<br />
I had this opportunity during a scientific visit in<br />
Moscow in Summer 1992. The collection is still housed<br />
in Dr. Nazarov's former working room in the Institute and<br />
is in good condition. The skeletons: are fixed in<br />
permanent embedding medium as preparations of whole<br />
residues. Drawing from light microscope is in my<br />
opinion the only way to provide clearer illustrations. The<br />
address of the Geological Institute: Geological Institute of<br />
the Academy of Science, Pyzhevsky Pereulok D-7,<br />
109017 Moscow, Zh 17, Russia.<br />
Andreas Braun<br />
local biostratigraphic resolution by grouping forms for<br />
the sake of correlation. In many cases a revaluation of the<br />
samples, to find the subspecies was necessary to reestablish<br />
the lost resolution.<br />
Our data base consists now of <strong>radiolaria</strong>n occurrence<br />
data from over 1500 samples from 130 measured sections<br />
of the Middle Jurassic to Early Cretaceous time interval,<br />
recovered from the Tethyan-Circumpacific low<br />
paleolatitude realm. Sample localities include the Alpine<br />
Mediterranean area, Central and Eastern Europe, Oman,<br />
Japan, parts of Western North America, Central America<br />
and most low paleolatitude DSDP - ODP sites in the<br />
Oceans.<br />
The contributors agreed on using the Unitary<br />
Associations method to integrate individual data sets into<br />
a common zonation. Unitary Associations (U.A.) are<br />
calculated with the program BIOGRAPH (J. Savary and J.<br />
Guex, Institut de Géologie, University of Lausanne). The<br />
U. A. method creates a synthesis of the co-occurrences of<br />
taxa observed in all samples from all sections. The<br />
program BIOGRAPH produces a co-occurrence chart of<br />
chronologically ordered U. A., in which the maximum<br />
range of each species is displayed with respect to the<br />
maximum ranges of all other species. In general, several<br />
U.A. are grouped to define a biochronozone, to insure the<br />
optimum of lateral reproducibility, and superpositional<br />
control of zones in as many sections as possible.<br />
Besides the species group problems mentioned above,<br />
BIOGRAPH helped us to realize, that we, the WGmembers<br />
have all a certain degree of specialization, i. e.
Radiolaria 14 News<br />
we have our pets that we know well and determine easily,<br />
whereas we tend to doubt about other species which we do<br />
not know so well. A logical consequence of this human<br />
preference is the incoherence of our datasets. Correlation<br />
by BIOGRAPH is entirely based on species association or<br />
exclusion and on superpositional relationships between<br />
species and species associations. Incomplete data, in our<br />
case simply caused by the specialization of each worker,<br />
result in huge numbers of undetermined relationships, and<br />
hence poor superpositional control and poor lateral<br />
reproducibility of Unitary Associations.<br />
The new biozonation presented in our Atlas represents<br />
a synthesis of a number of local biozonations based on<br />
What is going on in the Cenozoic?<br />
Material from recent ODP legs in the Antarctic has<br />
resulted in a number of biostratigraphic and taxonomic<br />
studies in the high Southern latitudes. Other studies of<br />
importance are: description of Paleocene faunas from the<br />
Indian Ocean and New Zealand, biogeographical and<br />
paleoecological studies in the equatorial Pacific, flux<br />
pattern studies in the Southern Ocean, a detailed<br />
morphological study of the Pyloniacea and a report on the<br />
Tripyleans in the Subantarctic. Marine pollen and<br />
siliceous microfauna have been reported to record<br />
concurrent late glacial variations in the regional terrestrial<br />
and marine environments around the Okhotsk basin.<br />
Comparisons of Late Miocene to Recent <strong>radiolaria</strong>ns from<br />
the Oman margin with the fauna recovered from the Peru<br />
margin upwelling area suggests that the assemblage may<br />
be globally diagnostic of upwelling conditions;<br />
strengthening and weakening of upwelling pulses is<br />
indicated by marked faunal changes. A study of the origin<br />
and the evolution of the Pterocorythidae through the<br />
Cenozoic reveals that there are only two persistent stocks<br />
from which developed fourteen branches treated as genera<br />
and subgenera; interesting trends in abundance and<br />
geographic distribution have been documented in this<br />
family. Comparison of assemblages from plankton and<br />
sediments in the Norwegian fjords and from stations in<br />
the Norwegian Sea, using multivariate analysis, shows<br />
that the largest source of variability is between sediment<br />
and plankton, differences due to season, region and depth<br />
are secondary.<br />
The Cenozoic working group has not had a joint<br />
project, but several of its members have had close<br />
working relationships resulting in valuable scientific<br />
publications which can be seen in the above list of<br />
publications and from the following summary:<br />
News items:<br />
1) Simon K. Haslett (University OF East Anglia) visited<br />
Annika Sanfilippo at Scripps Institution of Oceanography<br />
on a Fulbright Scholarship (October 19, 1992 - Jan 4,<br />
1993). Mr Haslett works on modern distributional<br />
Cenozoic Working Group News<br />
Catherine Nigrini and Annika Sanfilippo<br />
- 9 -<br />
BIOGRAPH calculations. We realized, that sacrifices of<br />
local stratigraphic resolution are unavoidable to achieve a<br />
worldwide correlation. However, the large number of<br />
included taxa results in a good temporal resolution (about<br />
80 U.A. for the Middle to Upper Jurassic and 35 U.A. for<br />
the Lower Cretaceous). We create about 20 zones for the<br />
Aalenian - Barremian interval. Chronostratigraphic<br />
calibration was obtained by correlation to ammonites,<br />
calpionellids, nannofossils etc., and magnetic polarity<br />
zones.<br />
Peter O. Baumgartner<br />
patterns of <strong>radiolaria</strong>ns in the East tropical Pacific. During<br />
his visit Mr. Haslett sampled a number of coretops from<br />
the Scripps core collection to compliment his own<br />
samples from ODP Site 677A and 846 in the<br />
Olduvai/Gauss time interval.<br />
2) Donna Hull and Annika Sanfilippo participated in<br />
fieldwork conducted in Cuba from January 11-16, 1993 in<br />
conjunction with the International Geological<br />
Correlations Project #308 (Paleocene-Eocene boundary).<br />
The purpose was to review stratigraphic work in Cuba on<br />
three potential boundary stratotypes and to resample the<br />
sections in detail. Five geologists from the U.S<br />
participated and were hosted by nine Cuban colleagues<br />
from the IGCP committee. The Cuban sections are of<br />
special interest as they contain both siliceous and<br />
calcareous microfossils. Biostratigraphic work on the<br />
sections by Gena Fernandez (planktonic foraminifera) and<br />
Emilio Florez (Radiolaria) has provided the basic<br />
stratigraphic framework. Joint efforts are now underway<br />
between the US and the Cuban team to produce results by<br />
the fall of 1994.<br />
3) During the months of May, 1993 and February, 1994<br />
Dr. Jean-Pierre Caulet (Laboratoire de Geologie, Museum<br />
National d'Histoire Naturelle, Paris, France) visited<br />
Annika Sanfilippo at Scripps Institution of Oceanography<br />
to work on <strong>radiolaria</strong>n evolution in the Antarctic.<br />
4) Annika Sanfilippo and Amy Weinheimer finished the<br />
preparation of the <strong>radiolaria</strong>n samples from DSDP Legs 1-<br />
96 (3000 samples) for the eight DSDP/ODP<br />
Micropaleontological Reference Centers (MRC) around<br />
the world. The material is available at a MRC near you to<br />
compare prepared material with the reports and<br />
illustrations published in the DSDP Initial Reports. This<br />
will help stabilize taxonomy, enable researchers to view<br />
material for biostratigraphic and paleoenvironmental<br />
purposes and prior to a cruise, to better plan subsequent<br />
sample requests from the DSDP/ODP repository.<br />
5) During the months of October and November, 1993<br />
Catherine Nigrini (510 Papyrus Drive, La Habra Heights,<br />
CA 90631) held the position of professor at the Museum<br />
National d'Histoire Naturelle in Paris where she worked
News Radiolaria 14<br />
with J.P. Caulet on Late Neogene cores from the central<br />
Indian Ocean basin.<br />
6) Amy Weinheimer is defending her PhD. thesis<br />
entitled: "Radiolarian and Diatom Fluxes in Two<br />
California Borderland Basins as Indices of Climate<br />
Variability" at the University of California Santa Barbara<br />
on April 4, 1994. She has a postdoc at Scripps Institution<br />
of Oceanography and will continue work on evaluating<br />
the relationships between annual <strong>radiolaria</strong>n fluxes from<br />
the Santa Barbara Basin and physical oceanographic and<br />
atmospheric data together with Dan Cayan and Tim<br />
Baumgartner.<br />
7) Annika Sanfilippo and Catherine Nigrini have<br />
submitted a paper entitled "Radiolarian stratigraphy across<br />
the Oligocene/Miocene transition" to Marine<br />
Micropaleontology.<br />
ABSTRACT In the absence of a Paleogene\Neogene boundary<br />
stratotype containing Radiolaria, we propose that the<br />
position of the Oligocene\Miocene boundary, as defined by<br />
low latitude <strong>radiolaria</strong>ns in deep sea sediments, be changed.<br />
The base of the Lychnocanoma elongata Zone, defined by<br />
the first appearance of L. elongata, has frequently been<br />
taken as a first approximation to the Oligocene/Miocene<br />
boundary in low latitude sediments, although many authors<br />
have placed it at an unspecified level within the L. elongata<br />
Zone. Examination of the <strong>radiolaria</strong>n fauna in 12 low<br />
latitude DSDP sites containing the Oligocene/Miocene<br />
transition has resulted in the sequencing of 29 <strong>radiolaria</strong>n<br />
"events" and direct comparison between calcareous<br />
nannofossil and <strong>radiolaria</strong>n zonations. We have determined<br />
that the Oligocene Miocene boundary is closer to the last<br />
occurrence of Artophormis gracilis in the uppermost part of<br />
the L. elongata Zone. In practice, the first occurrence of<br />
Cyrtocapsella tetrapera, which is at about the same level as<br />
the last occurrence of A. gracilis, is a more reliable and<br />
more easily recognized event. In addition, C. tetrapera is<br />
found in sediments from all latitudes, whereas A. gracilis is<br />
restricted to low and middle latitudes. Placement of the<br />
boundary at the first occurrence of C. tetrapera is a closer<br />
approximation to the recently defined nannofossil proxy,<br />
the last appearance of Reticulofenstra bisecta. Hence, the<br />
base of the C. tetrapera Zone (defined by the first<br />
occurrence of C. tetrapera) can serve as a good<br />
cosmopolitan proxy for the epoch boundary.<br />
8) Annika Sanfilippo and Catherine Nigrini will be<br />
attending the ODP symposium on Micropaleontology<br />
sponsored by the British Micropaleontological Society in<br />
Aberystwyth, Wales, April 18-22, 1994, and presenting a<br />
Some updated Paleozoic info from those people who<br />
can be contacted by email (and actually reply) Bonnie<br />
Murchey I continuing work on Late Paleozoic <strong>radiolaria</strong>ns<br />
in the western U.S. (Cordillera). Currently, I am finishing<br />
up a manuscript correlating assemblages from several<br />
regions in the Cordillera. I have just submitted a short<br />
paper on the distribution of <strong>radiolaria</strong>ns and sponge<br />
spicules in the Ouachita orogen of Oklahoma (with<br />
emphasis on the late Carboniferous). As part of a USGS<br />
mapping project in the gold-mining districts of central<br />
Nevada, I am also doing a bit of work on Ordovician to<br />
Devonian faunas.<br />
Paleozoic Working Group News<br />
Jonathan C. Aitchison<br />
- 10 -<br />
poster, "Biostratigraphic Review and Recalibration of<br />
Paleogene Radiolarian zones in all Tropical DSDP/ODP<br />
Sediment Sequences (Legs 1-135)", and an oral<br />
presentation, "Radiolarian stratigraphy across the<br />
Oligocene/Miocene transition".<br />
ABSTRACT FOR POSTER The location and amount of<br />
biogenic silica deposition in the Paleogene Ocean reflects<br />
both the ocean chemistry and sea water circulation of that<br />
period and yields important clues for the reconstruction of<br />
paleoclimates and paleoproductivity. We have compiled a<br />
catalogue and chart of all low and middle latitude<br />
DSDP/ODP sites (through Leg 135) in which there is a<br />
recognizable <strong>radiolaria</strong>n fauna. These sites have been reexamined<br />
and correlated with available nannofossil zones<br />
and, where possible, with paleomagnetically derived ages<br />
so as to provide an internally consistent data set. Some<br />
zonal assignments have been revised to reflect changes in<br />
<strong>radiolaria</strong>n taxonomic and zonal concepts since the<br />
beginning of the Deep Sea Drilling Project. Using this data<br />
we have generated a series of time slice maps showing the<br />
paleolatitudes of silica rich sites. These maps provide a<br />
basis for examination of global processes involving silica<br />
deposition and dissolution during the Paleogene, indicate<br />
areas where evidence is lacking and suggest potentially<br />
fruitful locations for future recovery of silica rich<br />
Paleogene sediments.<br />
ABSTRACT FOR ORAL PRESENTATION see under section 7<br />
9) During the fall of 1992 Catherine Nigrini and Annika<br />
Sanfilippo prepared for the Ocean Drilling Program three<br />
complete and identical sets of 60 microscope slides each<br />
documenting Cenozoic low and middle latitude <strong>radiolaria</strong>n<br />
zones. Depending on the length of the zone there are one<br />
to three slides for each zone. The companion<br />
documentation, "Cenozoic <strong>radiolaria</strong>n stratigraphy for low<br />
and middle latitudes" providesstandardized species and<br />
zonal concepts to facilitate consistent stratigraphic<br />
interpretation. The volume includes descriptions of 160<br />
stratigraphically useful species with brief synonymies,<br />
morphologic descriptions, dimensions, distinguishing<br />
characters, variability, geographic and stratigraphic ranges,<br />
phylogenies and illustrations. Definitions of zones, a<br />
summary of <strong>radiolaria</strong>n events within each zone and a<br />
summary range chart has also been provided. One of these<br />
slide sets with the accompanying text is currently on the<br />
Ocean Drilling Program research ship, the Joides<br />
Resolution, to be used as a library and reference collection<br />
by shipboard micropaleontologists.<br />
Paula Noble has relocated to California and is<br />
finishing her first year as an Asst. Professor in the<br />
Geology department where she teaches historical geology,<br />
stratigraphy, paleo, oceanography, and anything else they<br />
need her to cover. Paula has taken a brief hiatus from<br />
research to get her courses underway, but plans to<br />
continue fieldwork on early Palezoic eugeoclinal rocks in<br />
Nevada in hopes of breaking out the Silurian from the<br />
Ordovician and in tieing it to work in west Texas. She<br />
hopes to also begin work in the Sierra Nevada foothills in<br />
the near future. This Fall, her monograph on the Silurian<br />
Caballos Novaculite was completed, and is slated to be<br />
the second Bulletin of American Paleontology for 1994.
Radiolaria 14 News<br />
James Stratford - University of Sydney. Devonian<br />
<strong>radiolaria</strong>n biostratigraphy in part of the Gamilaroi<br />
terrane, southern New England Orogen, N.S.W. Three<br />
<strong>radiolaria</strong>n assemblages are found in the Glenrock area.<br />
The faunal affinities of these assemblages are at present<br />
uncertain. Corals associated with the middle assemblage<br />
are ?Early Emsian, suggesting a Lower to lower Middle<br />
Devonian age range for these <strong>radiolaria</strong>ns.<br />
Jonathan Aitchison - University of Sydney.<br />
Continues to work on Lower Paleozoic <strong>radiolaria</strong>n<br />
biostratigraphy. Much of this work is concentrated on<br />
Devonian rocks of the Gamilaroi terrane, southern New<br />
England Orogen, N.S.W. It seems that good radiolairans<br />
are present in the Lower and Middle Devonian and<br />
Jonathan is hoping to have a preliminary biostratigraphy<br />
fleshed out before the Interrad meeting. Likewise with the<br />
- 11 -<br />
Silurian we have found good bugs - this time from Japan<br />
and are calibrating the stratigraphy using the SHRIMP to<br />
get U/Pb ages from pyroclastic zircons. When time<br />
permits Jonathan is also working on rads around the<br />
Cambro/Ordovician boundary from Newfondland as well<br />
as Ordovician material from the vast Lachlan Fold Belt of<br />
eastern Australia. Jonathan has also ventured up-section<br />
and looked at some Cretaceous from Sabah and New<br />
Caledonia as well as some Cenozoic from Leg 143 but<br />
reports that rads definitely improve with age and the<br />
Paleozoic is best!<br />
Hiroaki Ishiga (Shimane University) and his students<br />
have recently produced some publications on nicely<br />
preserved Ordovician <strong>radiolaria</strong>ns from the Lachlan Fold<br />
Belt in eastern Australia.<br />
News from the International Paleontological Association<br />
International Paleontological Association:<br />
General Assemnly, Kyoto, August, 1992<br />
Makoto Kato<br />
On the occasion of the 29th International Geological<br />
Congress in Kyoto, Japan, the IPA held two business<br />
meetings and a social gathering. All the activities took<br />
place in the Kyoto International Conference Hall. A<br />
welcoming beer party for palaeontologists participating in<br />
the IGC was held on the evening of August 25. The party<br />
was organized by the Palaeontological Society of Japan in<br />
conjunction with the IPA, and no less than 200<br />
palaeontologists enjoyed the occasion. The IPA Council<br />
Meeting was held on the afternoon of August 26. The<br />
agenda of the General Assembly was discussed in great<br />
detail. The IPA General Assembly was held on the<br />
evening of August 26, the same day as the Council<br />
Meeting. The Assembly was opened by the President,<br />
Prof. A, Hallam. The report of the last General<br />
Assembly, Washington, July 17,1989, was approved as<br />
published (W.A. Oliver, Jr., 1989, Lethaia 22, p.357).<br />
Then Secretary-General Kato reported on the IPA<br />
activities since the last General Assembly in Washington,<br />
in July 1989. The IPA sponsored three palaeontological<br />
symposia in l989, four in l990, four in l991 and so far<br />
one in 1992. Three volumes of Lethaia were published<br />
during the time of the present office holders. All the<br />
activities have been recorded in the IPA Annual Reports<br />
for 1989, 1990 and 1991, and in Lethaia, Vol. 24, pp.<br />
247-248, 1991; Vol. 25 p. 351, 1992. The Executive<br />
Committee was consulted on the problem of<br />
constitutional amendments and the necessity of raising<br />
membership dues. A nominating committee was set up in<br />
preparing a slate of candidates for new IPA officers. These<br />
were further discussed at the General Assembly. As<br />
regards the IPA finances, Treasurer Kaesler reported that<br />
we supported a number of symposia, as recorded above,<br />
and had been continuously building funds for future<br />
publication of directories. Due to general withdrawal of<br />
Lethaia Forum - IPA; Lethaia vol. 26, 1993<br />
Jonathan C. Aitchinson<br />
the IUGS in allocating funds to the IPA, however, we<br />
now provide US$ 500 to each appropriate<br />
palaeontological symposium for seed money, instead of<br />
giving $1000 as informer days, and expect the sum to be<br />
returned when the symposium is successfully concluded.<br />
A substantial part of the IPA income has been borne<br />
by Lethaia. With the approval of the Executive committee<br />
the IPA asked the Lethaia Foundation for an increase of<br />
dues. They now generously give $9 for each IPA member<br />
subscribing to Lethaia instead of $5 as before.<br />
The Committee of Auditors (Professor Richard A.<br />
Robison and Dr. Chris G. Maples) reported that the<br />
Treasurer's accounts and records were in excellent order.<br />
The Treasurer announced that there were regrettably some<br />
corporate members who did not promptly pay their dues.<br />
The following corporate members, research groups and<br />
symposia submitted their reports to the IPA: International<br />
Paleozoic Microvertebrate Working Group (now IGCP<br />
328), International Research Group on Charophytes<br />
(IRGC), Graptolite Working Group, Colloquium<br />
"Paleontologie et stratigraphie d'Amerique latine", All-<br />
Union Paleontological Society of Russia, Swiss<br />
Palaeontological Society, and European Palaeontological<br />
Association. Reports were circulated amongst those<br />
attending.<br />
Subsequently the Webby proposal for the amendment<br />
of the IPA Constitution and By-Laws was discussed. At<br />
the last IPA General Assembly Professor Barry Webby<br />
proposed to formally include in the IPA activity the<br />
publication of the fossil Collections of the World: an<br />
International Guide. His proposal and wording of the<br />
amendments of the IPA Constitution and By-Laws were<br />
published in the IPA Annual Report for 1989. Later the<br />
IPA Executive Committee approved this proposal. After<br />
some discussions at the General Assembly the<br />
Constitution was changed as follows: To the Article<br />
11.(2) of the Statutes for the list of IPA activities<br />
"Publication of the Fossil Collections of the Worlds: an<br />
International Guide" was added.
News Radiolaria 14<br />
Furthermore By-Law (3) was amended thus: 'The<br />
World Directory of Palaeontologists and the Fossil<br />
Collections of the World: an International Guide. Both the<br />
World Directory of Palaeontologists and the Fossil<br />
Collections of the World: an International Guide should<br />
be revised and a new edition published every eight years.<br />
Every member may be provided with free copies of these<br />
volumes, but this will depend on the current financial<br />
circumstances of the Association. For archiving of the<br />
IPA records, agreement of transfer between the<br />
Smithsonian Institution and the IPA was formally<br />
approved and President Hallam signed the document on<br />
behalf of the IPA. Full text of the agreement is to be<br />
found in the IPA Annual Report for 1991, p. 20.<br />
The report of the Nominating Committee, consisting<br />
of Drs. F. Debrenne, R. Grant, J. Jell, Z. Kielan-<br />
Jaworowska, M. Zhou and M. Kato (chairman ex officio),<br />
was distributed, an as no additional nominations had been<br />
received, the following officers were elected unanimously.<br />
President, Prof. Chang, Mee-mann, China; Vice-<br />
Presidents, Prof. D.L. Kaljo, Estonia, Dr. R.A. Cooper,<br />
New Zealand, Prof. A.C. Riccardi, Argentina, Prof. P.<br />
Taquet, France; Secretary-General, Prof. D.L. Bruton,<br />
Norway; Treasurer, Prof. R.L. Kaesler, USA; Membersat-Large,<br />
Dr. S. Bengtson, Sweden, Prof. B. Runnegar,<br />
USA; Past President, Prof. A. Hallam, UK; and Past<br />
Secretary-General, Prof. M. Kato, Japan.<br />
For future activity, it was generally agreed that the<br />
IPA should continue to support organizing international<br />
palaeontological symposia, colloquia, etc. The IPA<br />
should take every measure to promote palaeontology, in<br />
protesting about, for instance, cutbacks and job losses,<br />
and promoting a higher visibility of our discipline, or in<br />
drawing public attention to the need for conservation of<br />
famous sites for fossil collection, or the need for<br />
improved curation of museum specimens.<br />
Prof. P. Sartenaer raised the question of<br />
palaeontological collections in danger. Private collections<br />
and institutional collections having no person to look<br />
after them are both inaccessible and susceptible to damage<br />
and eventual loss. We need information on those<br />
collections that should be moved to a public museum.<br />
IPA action along these lines was felt to be appropriate and<br />
the point will be conveyed to the next IPA office holders.<br />
There being no other business, President Hallam<br />
thanked all the attending members of the assembly for cooperation,<br />
his fellow officers and committee members for<br />
The 1995 drilling schedule will be decided at<br />
December's Planning Committee meeting. For more<br />
information on Ocean Drilling and other JOIDES<br />
activities, write to Joint Oceanographic Institutions, Inc.,<br />
1755 MassachusettsAve.,NW, Suite800, Washington,<br />
D.C., 20036-2102, U.S.A.; Phone: 202-232-3900;<br />
Ocean Drilling Program News<br />
Joint Oceanographic Insitution for Deep Earth Sampling<br />
- 12 -<br />
their efforts, and the International Research Group officers<br />
and Symposium organizers for their efforts. He then<br />
declared the General Assembly adjourned. The Assembly<br />
expressed thanks to all retiring officers for their services.<br />
Makoto Kato (Past Secretary General, IPA),<br />
Department of Geology and Mineralogy, Faculty of<br />
Science, Hokkaido University, N10, W8, Sap-poro<br />
060, Japan; 30th November, 1992.<br />
International Palaeontological Association<br />
records to be archieved<br />
Ellis L. Yochelson<br />
The International Paleontological Union, founded in<br />
1933, was reorganized as the International<br />
Palaeontological Association in 1968. Since its founding,<br />
there have been 13 sets of officers. In keeping with the<br />
International aspect of the group, officers have resided in<br />
many countries, on three continents. Thus the records of<br />
IPA/IPU are widely scattered.<br />
Arrangements have now been made with the<br />
Smithsonian Institution Archives in Washington, D.C.,<br />
to deposit the papers of the Association. From the<br />
inception of IPA in 1968, three treasurers and one<br />
secretary-general of the organization have been affiliated<br />
with the National Museum of Natural History,<br />
Smithsonian Institution. For those who are familiar with<br />
Washington, the Smithsonian Institution Archives is<br />
located in the 'Arts & Industries' Building, a red brick<br />
structure to the east of the Smithsonian 'Castle'. The<br />
Archives is open, five days a week, to all qualified<br />
investigators.<br />
Anyone who has material concerning IPA or its IPU<br />
predecessor (including photographs of officers and of<br />
meetings) is asked to send items to Ellis L. Yochelson<br />
(address below) or to David L. Bruton, Secretary-General<br />
IPA, Paleontologisk Museum, Sars Gate I, N-0562 Oslo,<br />
Norway. An historical summary, 'The International<br />
Palaeontological Association: Historical Perspective' was<br />
published by Curt Teichert and Ellis Yochelson in<br />
Episodes 8:4, 252-255, 1985.<br />
Ellis L. Yochelson, Department of Paleobiology,<br />
National Museum of Natural History, Washington,<br />
DC 20560, USA.<br />
Internet: joi@iris.edu; to request copies of the JOIDES<br />
Journal.<br />
To apply for participation as a shipboard scientist on<br />
an ODP cruise, send a letter of request and a resume to the<br />
Manager of Science Operations, Ocean Drilling Program,<br />
Texas A&M University Research Park, College Station,
Radiolaria 14 Symposia<br />
TX, 77845. You will receive an application form to fill<br />
out and return to ODP.<br />
ODP Sets 1995 Drilling<br />
ODP is currently staffing Legs 159 onwards.<br />
Shipboard participation is by invitation from ODP's<br />
science operator at Texas A&M University. Information<br />
and applications can be obtained by contacting the Ocean<br />
Drilling Program. Texas A&M Univesity, 1000<br />
Discovery Drive, College Station, TX 77845-9547 or<br />
phone 409-845-2673, fax 409- 8454857, Internet:<br />
baldauf@nelson.tamu.edu.<br />
Leg 159 Return to Site 735<br />
The purpose of this leg is to return to ODP site 735<br />
on the southwest Indian Ridge, and deepen hole 735B to a<br />
nominal depth of 2 ~m mbsf. The principle objective of<br />
this proposed leg is to understand the nature of the<br />
processes involved in the generation of the lower crust,<br />
and the put some constraints on the lower crustal<br />
stratigraphy at the slowest end of the spreading spectrum.<br />
Leg 160 Eastern Eq. Atlantic Transform<br />
The key issues to be addressed by drilling include an<br />
evaluation of the tectonic and sedimentary processes<br />
involved in the creation of the main morpho-structural<br />
features ~enerated at the Cate d'Ivoire-Ghana Transform<br />
Margin. Results should provide data on the timing, rate<br />
and de~ree of vertical motion (subsidence and uplift) of the<br />
Cote d"Ivoire-Ghana Transform Margin.<br />
Leg 161/162 Mediterranean I & II<br />
The proposed two lef!s of drilling in the<br />
Mediterranean will address three main objectives: the<br />
- 13 -<br />
Alboran Basin (Western Mediterranean), drilling on the<br />
Mediterranean Accretionary Complex (Eastern<br />
Mediterranean), and an E-W transect across the<br />
Mediterranean Sea to sample and study organic-rich layers<br />
called Sapropels.<br />
Leg 163 N. Atlantic Arctic Gateways<br />
This is the second of two North Atlantic-Arctic<br />
Gateways (NAAG) legs. The first leg, ODP Leg 151 was<br />
drilled August - September of 1993. The scheduled second<br />
le~ of NAAG drilling will focus on the same goals as<br />
NAAG I but will also collect cores to try and resolve<br />
millermial scale climate variability and provide links to<br />
ice core data.<br />
Leg 164 Gas Hydrates<br />
Gas hydrates are a solid phase composed of water and<br />
low molecular weight gases (~redominantly methane)<br />
which form under conditions of low temperature, high<br />
pressure, and gas saturation; conditions that are common<br />
in the upper few hundred meters of rapidly accumulating<br />
marine sediments. The main o6jechves of the proposed<br />
leg are to investigate the in situ characteristics of gas<br />
hydrates.<br />
Leg 165 Test of the DCS<br />
Throughout the past six years the Ocean Drilling<br />
Program has expended considerable effort on the design<br />
and development of a Diamond Coring System (DCS).<br />
The Planning Committee has tentatively scheduled an<br />
engineering leg during which the prime objective will be<br />
a test of the diamond coring system and in particular the<br />
secondary heave compensation system.<br />
Report of "Radiolarian events" Symposium<br />
International Geological Congress, Kyoto, Japan August, 1992<br />
Symposium "Radiolarian events" of IGC (29th<br />
International Geological Congress) held on August 24-25<br />
convened by Drs. Patrick DE WEVER (Univ. Pierre et<br />
Marie-Curie, France), WANG Naiwen (Chinese Acad.<br />
Geol Sci., China) and Akira YAO (Osaka City Univ.,<br />
Japan) in the Kyoto International Conference Hall.<br />
Twenty-two abstracts were submitted covering<br />
biostratigraphy, paleobiogeography and paleoecology of<br />
Phanerozoic <strong>radiolaria</strong>ns. (Two presentations were<br />
canceled.) The following was the program of symposium<br />
Chairpersons: P. DE WEVER and A. YAO;<br />
A. ORAL SESSION (August 24, 1992)<br />
Aita, Y.: Triassic and Jurassic high latitude <strong>radiolaria</strong>n<br />
faunas from New Zealand<br />
Blome, C.D. and Reed K.M.: Permian <strong>radiolaria</strong>n<br />
faunas in the Grindstone terrane of central Oregon and<br />
their similarities to coeval Japanese faunas<br />
Akira Yao<br />
Joides Journal, February 1994<br />
Hori, R.: Radiolarian Toarcian event recorded in bedded<br />
cherts from Japan<br />
Ishida, K.: Radiolarian assemblage from the<br />
Kimmeridgian ammonite-bearing formation of the<br />
Torinosu Group in East Shikoku, Southwest Japan<br />
Ishiga, H.: Recent progress of the Paleozoic <strong>radiolaria</strong>n<br />
biostratigraphy<br />
JURASSIC-CRETACEOUS WORKING<br />
GROUP (Baumgartner, P.O.; Gorican S.; Jud,<br />
R.; O'Dogherty L. [co-leaders], Conti, M.; Danelian,<br />
T.; De Wever, P.; Dumitrica, P.; Kito, N.; Marcucci, M.;<br />
Matsuoka, A.; Steiger, T. and Urquhart, E. [principal<br />
contributors]: Middle Jurassic-Early Cretaceous <strong>radiolaria</strong>n<br />
biochronology of Tethys and Circum-Pacific low<br />
paleolatitudes<br />
Ling, H.Y.: Paleogene <strong>radiolaria</strong>n events<br />
Matsuoka, A.: Low-latitude Middle Jurassic to Lower<br />
Cretaceous <strong>radiolaria</strong>n stratigraphy in the western Pacific
Symposia Radiolaria 14<br />
Noble, P. and Aitchison, J.: Development of a<br />
global Silurian <strong>radiolaria</strong>n biozonation<br />
Vishnevskaya, V.: The evolution of <strong>radiolaria</strong>n<br />
foramen is possible evidence of the transition from<br />
benthos to plankton<br />
B. POSTER SESSION (August 25, 1992)<br />
Funakawa, S.: Classification of Plagoniidae<br />
(Nassellaria, Radiolaria) based on internal skeletal<br />
structure<br />
Goto, H.; Umeda, M. and Ishiga, H.: Ordovican<br />
and possible Cambrian <strong>radiolaria</strong>ns from the Lachlan Fold<br />
Belt, southeastern Australia<br />
Ishida, K.: Radiolarian assemblage from the<br />
Kimmeridgian ammonite-bearing formation of the<br />
Torinosu Group in East Shikoku, Southwest Japan: note<br />
on the age of Stylocapsa (?) spiralis Assemblage-zone<br />
Ishiga H. and Ishida, K.: Revision of Middle to<br />
Upper Permian <strong>radiolaria</strong>n zonation of Southwest Japan<br />
- 14 -<br />
Iwata, K., Watanabe, T. and Leitch, E.C.:<br />
Middle Ordovician <strong>radiolaria</strong>ns of the Lachlan Fold Belt,<br />
New South Wales, eastern Australia<br />
Iwata, K.: Late Cretaceous and Paleogene <strong>radiolaria</strong>ns<br />
of Hokkaido<br />
Soeka, S. and Mudjito : Early Cretaceous-Paleogene<br />
<strong>radiolaria</strong>n biostratigraphy from the microcontinent of<br />
Buton, eastern Indonesia<br />
Spencer-Cervato, C.; Lazarus, D.B.;<br />
Beckmann, J.P.; von Salis Perch-Nielsen, K.<br />
and Biolzi, M.: New calibration of Neogene<br />
<strong>radiolaria</strong>n events in the north Pacific<br />
Vishnevskaya, V.: Correlation of Tethyan and Pacific<br />
<strong>radiolaria</strong>n events during Middle-Late Mesozoic<br />
Yao, A.: Progress in Triassic and Jurassic <strong>radiolaria</strong>n<br />
biostratigraphy<br />
Report of "Radiolaria: application for stratigraphy, paleogeography and<br />
paleotectonics"symposium<br />
L.P. Zonenshain Memorial Conference on Plate tectonics Symposium, Moscow, Russia, November 1993<br />
This symposium was a part of L.P. Zonenshain<br />
Memorial Conference on Plate tectonics held on<br />
November 17-20 in Moscow, organized by the Institute of<br />
Oceanology (Russian Academy of Sciences) and<br />
GEOMAR (Christian-Albrechta University, Kiel,<br />
Germany). About 40 talks and posters concerning<br />
<strong>radiolaria</strong>ns were presented, 28 abstracts were submitted.<br />
The importance of <strong>radiolaria</strong>n age constraints in<br />
tectonic and paleogeographic studies was emphasized.<br />
Recent development of using <strong>radiolaria</strong>ns as paleolatitude<br />
and environment indicators was presented. Major Permian<br />
to Cretaceous <strong>radiolaria</strong>n faunal changes were discussed.<br />
The book of abstracts is available through Valentina<br />
S. Vishnevskaya who was the main organizer of this<br />
<strong>radiolaria</strong>n symposium.<br />
RADIOLARIA: APPLICATION FOR STRATIGRAPHY,<br />
PALEOGEOGRAPHY AND PALEOTECTONICS<br />
(SYMPOSIUM 8B)<br />
Conveners: De Wever, P.; Vishnevskaya, V.S. and<br />
Kruglikova, S.B.<br />
ORAL SESSION (Friday 19, November 1993)<br />
Afanasieva, M.S.: Possible reasons for the<br />
appearance, biomineralization and fossilization of<br />
<strong>radiolaria</strong>n siliceous skeletons and paleobiogeographic<br />
reconstruction for the Early Permian<br />
Spela Gorican and Valentina S. Vishnevskaya<br />
Akira Yao<br />
Aitchison, J.C.: Radiolarians, a key to contrasting the<br />
tectonic evolution of orogenic zones worldwide:<br />
examples of their application and suggestions of future<br />
potentials<br />
Bragin, N.Yu.: Boreal <strong>radiolaria</strong>n assemblages of the<br />
Triassic and Jurassic and their significance for tect and<br />
paleogeographic interpretations<br />
De Wever, P.; Azema, J. and Fourcade, E.:<br />
Radiolarians and radiolarites: from primary production to<br />
paleogeography<br />
Gorican, S.: Jurassic and Cretaceous <strong>radiolaria</strong>n<br />
biostratigraphy and sedimentary evolution of the Budva<br />
zone (Dinarides, Montenegro)<br />
Hori, R.: Origin of Early Jurassic <strong>radiolaria</strong>n faunal<br />
changes recorded in bedded chert from the Nino complex,<br />
Japan<br />
Khokhlova, I.E.: Paleogene <strong>radiolaria</strong> of the North<br />
Tethys: taxonomic composition and paleoecological<br />
reconstructions<br />
Kruglikova, S.B.: High-rank taxa of Radiolaria as an<br />
indicator of paleoenvironment<br />
Marcucci, M.: Jurassic <strong>radiolaria</strong>n cherts in the<br />
Northern Apennines<br />
Matul, A.: Paleoceanographic changes in the northern<br />
North Atlantic for the last 13 Ka interpreted from<br />
<strong>radiolaria</strong>n data (core MK-340, Reykjanes Ridge)
Radiolaria 14 Symposia<br />
Ormiston, A.: Using Paleozoic <strong>radiolaria</strong>ns to define<br />
paleolatitudes and identify allochthonous terranes<br />
Tochilina, S.V. : Comparative characteristics of a<br />
Middle Miocene hiatus in the Philippine Sea based on r<br />
5 DSDP data Leg 59, Site 126<br />
Urquhart E. and Robertson, A.: Radiolaria and the<br />
structural evolution of Cyprus in the Late Cretaceous<br />
Vishnevskaya, V.S.: Important <strong>radiolaria</strong>n events of<br />
the north-western Pacific region<br />
POSTER SESSION (Thursday 18, November 1993)<br />
Agarkov, Yu.V. : Radiolarian potential of the Pre-<br />
Caucasus<br />
Antadze, M.: Jurassic - Early Cretaceous <strong>radiolaria</strong> in<br />
alkali volcano-sedimentary series of the Lesser Caucasus<br />
and Eastern Pontides<br />
Aparin, V.P. and Zolotova, O.P.: Analysis of<br />
time series data for geodynamic processes<br />
Borisov, B.A. and Lipman, P.Kh.:<br />
Paleogeographical importance of <strong>radiolaria</strong>ns from<br />
pebbles of Cretaceous alluvium from the Zaisan trough,<br />
North Eurasia (East Kazakhstan)<br />
Bragin, N.Yu. and Bragina, L.G.: Radiolarian<br />
biostratigraphy of Upper Cretaceous deposits in<br />
Southwestern Cyprus<br />
Ellis, G.: Early Cretaceous <strong>radiolaria</strong> from the<br />
Carnarvon basin Western Australia<br />
Fedotova, A.A.: Carbonate shelf destruction related to<br />
the closure of marginal basins (southeastem part of<br />
Eastem Sayan)<br />
Glevassky, E.B. and Kalyaev, G.I.: Iron-cherty<br />
formations as indicators of geodynamic situations<br />
I.A. Basov and A. Yu Gladenkov: Cenozoic<br />
biostratigraphy of the Subarctic Pacific (ODP, Leg 145)<br />
Ivanova, E.V. and Ivanova, A.A.: Neogene<br />
paleogeodynamic reconstructions and climatic zonation<br />
of the In Ocean: New results based on ODP data<br />
Kasintsova, L.I.: Radiolaria from Albian<br />
terrigeneous-carbonate rocks of eastern Europe<br />
Krasheninnikov, V.A.; Kazarina, G.Kh.;<br />
Kruglikova, S.B.; Mikhina, V.V. and<br />
Ushakova, M.G.: Use of planktonic mlcrofossils for<br />
the study of stratigraphy of deposits and<br />
paleoenvironment of the East Pacific<br />
Krimsalova, V.T.: Radiolarian assemblages from the<br />
Raritkin Ridge (North Eastern Russia) and their<br />
paleogeographic affinity<br />
Lipman, R.Kh.: The first Russian investigation of<br />
<strong>radiolaria</strong>ns from deepwater sediments of the NW Pacific<br />
and their significance<br />
- 15 -<br />
Mallan-Dalla Piazza, P.: Integrated biochronology:<br />
<strong>radiolaria</strong>n, foraminifera and calcareous nannofossils<br />
from 13 sites from the Indian Ocean<br />
Malkin, B.V. : Geodynamic nature of<br />
geomorphological cycles<br />
Marcucci, M., Chiari, M. and Cortese, G.:<br />
Radiolarian biostratigraphy in the Jurassic cherts of the<br />
Northern Apennines<br />
Oleinik, L.: Some assemblages of Jurassic <strong>radiolaria</strong><br />
from Primorye (far eastem Russia)<br />
Philippova, I.B.; Kulikova, L.I.; Suetenko,<br />
O. and Kalimulin, S.M.: First set of maps for the<br />
Paleogeographic Atlas of Northern Eurasia<br />
Pralnikova, I.G.: Jurassic <strong>radiolaria</strong>ns from the<br />
Kingiveem volcano-sedimentary complex (Kuyul<br />
ophiolites, Talovka-Pekulney zone, NE Russia) as an<br />
indicator of palaeolatitude Rise and the Galapagos<br />
spreading zone in Pliocene-Quaternary time<br />
Scherba, I.G.: Paleogeography and tectonics of the<br />
Paleogene basin of the Caucasus<br />
Schultz, S.S. jr: Remote sensing information for the<br />
study of recent crustal movements<br />
Shikova, T.N. and Vishnevskaya, V.S. :<br />
Campanian to early Maastrichtian <strong>radiolaria</strong> from<br />
carbonaceous lenses of the Olyutor Ridge (Koryak<br />
Upland, Russia)<br />
Smimova, O.L.: Lower and Middle Jurassic <strong>radiolaria</strong><br />
of the South Sikhote-Alin L.B. Tikhomirova: New<br />
siliceous biostratigraphy of the Gorinsky synclinorium<br />
(far eastern Russia) based on <strong>radiolaria</strong>n data<br />
Stupka, O.S.: A model for the Early Mesozoic<br />
evolution of the Carpathian-Black Sea segment of the<br />
continental margin of the Tethys ocean. The<br />
stratigraphy of Cenozoic sediments and the age of<br />
manganese nodules in two areas of the Clarion-<br />
Clipperton province in the Pacific Ocean<br />
Vishnevskaya, V.S.: Late Cretaceous <strong>radiolaria</strong> of the<br />
Russian platform and comparison with the same faunas<br />
from Tethyan and Pacific regions<br />
Vishnevskaya, V.S. and Antadze, M.: Jurassic-<br />
Early Cretaceous <strong>radiolaria</strong> in alkali volcano-sedimentary<br />
series of the lesser Caucasus and eastern Pontides<br />
Vitukhin, D.I.: Radiolarians and their<br />
paleoenvironments in the Cenozoic deposits of far<br />
eastern Russia<br />
Volokitina, L.P. and Sedov, A.P.: Main<br />
morphological features of paleocean relief<br />
S. Gorican and V.S. Vishnevskaya
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Radiolaria Editor (lodogher@igp.unil.ch). Electronic mail<br />
is faster and much easier (and cheaper!)<br />
E-mail addresses of some <strong>radiolaria</strong>n paleontologists<br />
AITCHISON, Jonathan : jona@es.su.oz.au<br />
ANDERSON, Roger : ora@ldgo.columbia.edu<br />
BAUMGARTNER, Peter O.: pbaumgar@igp.unil.ch<br />
BJORKLUND, Kjell : kjell.bjorklund@toyen.uio.no<br />
BOLTOVSKOY, Demetrio : postmaster@plankt.edu.ar<br />
BRUNNER, Charlotte A.: cbrunner@whale.st.usm.edu<br />
CAULET, Jean-Pierre. : caulet@cimrs1.mnhn.fr<br />
CARTER, Beth : I1EC@cc.pdx.edu<br />
DANELIAN, Taniel : tdanelia@glg.ed.ac.uk<br />
ELLIS, Glynn: gellis@igp.unil.ch<br />
ESCO Secretariat : bj@dgu1.dgu.min.dk<br />
GORICAN, Spela : spela.gorican@uni-lj.si<br />
GOWING, Marcia : gowing@cats.ucsc.edu<br />
GUEX, Jean : jguex@igp.unil.ch<br />
HULL-MEYERHOFF,Donna : dmhull@utdallas.edu<br />
ISHIGA, Hiroaki : g01483@sinet.ad.jp<br />
ISHMAN, Scott E. : sishman@isdres.er.usgs.gov<br />
LAZARUS, David : gonzo@erdw.ethz.ch<br />
Electronic Mail Directory<br />
Demetrio Boltovskoy and Luis O'Dogherty<br />
INTERRAD VII, OSAKA<br />
- 16 -<br />
LEVENTER, Amy: rschere@ohstmvsa.acs.ohio-state.edu<br />
LIPPS, Jere : jlipps@ucmp1.berkeley.edu<br />
MALLAN-DALLA PIAZZA, P. : pmallan@igp.unil.ch<br />
MARINE MICROPAL. : b.westerop@elsevier.nl<br />
MOORE, Ted (internet) : ted.moore@um.cc.umich.edu<br />
MOORE, Ted (omnet) : t.moore@omnet.nasa.gov<br />
MORLEY, Joe : morley@ldgo.columbia.edu<br />
MURCHEY, Bon : bmurchey@usgs.gov<br />
NIGRINI, Catherine : 74710.2367@compuserve.com<br />
O'DOGHERTY, Luis : lodogher@igp.unil.ch<br />
PISIAS, Nick : pisias@oce.orst.edu<br />
POPOVA, Irina : fegi@visenet.iasnet.com<br />
RAMARUI,Jenny (ODP journal) : joramaru@brook.edu<br />
RIEDEL, Bill : wriedel@sdsioa.ucsd.edu<br />
RIEDEL, Bill : 71611.1047@compuserve.com<br />
ROBERTSON, A.H.: ahrobert@glg.ed.ac.uk<br />
SANFILIPPO, Annika : wriedel@odpwcr.ucsd.edu<br />
SCHAAF, Andre : aschaaf@illite.u-strasbg.fr<br />
SWANBERG, Neil (internet) : neil@igbp.kva.se<br />
SWANBERG, Neil (omn.): n.swanberg@omnet.nasa.gov<br />
TONIELLI, Renato : dottrig@itcaspur<br />
URQUHART, Elspeth : ucfbexu@ucl.ac.uk<br />
VON RAD, Ulrich : vonrad@gate1.bgr.d400.de<br />
WELLING, Leigh : welling@oce.orst.edu<br />
YAO, Akira : h1682@ocugw.cc.osaka-cu.ac.jp<br />
YOUNG, Jeremy R. (INA Editor) : jy@nhm.ic.ac.uk<br />
Seventh Meeting of the International Association of Radiolarian Paleontologists. 1994. 10. 20-24<br />
The InterRad VII Conference will be held near Osaka,<br />
Japan, 20 to 24 October, 1994. The conference will be at<br />
the Inter-University Seminar House of Kansai (IUSK),<br />
about 30km northwest of Osaka City. The conference is<br />
sponsored by the Geological Society of Japan and the<br />
Palaeontological Society of Japan.<br />
PROVISIONAL SCHEDULE:<br />
18 Oct. (Tue) - 20 Oct. (Thu) Pre-conference Excursions I<br />
and II<br />
20 Oct. (Thu) - 24 Oct. (Mon) InterRad VII conference<br />
20 Oct. Rendezvous at Osaka City University in the<br />
afternoon and travel to IUSK<br />
21-23 Oct. Symposium and general sessions<br />
24 Oct. Travel to Osaka City and disperse<br />
25 Oct. (Tue) - 27 Oct. (Thu) Post-conference Excursion<br />
- Second Circular -<br />
Atsushi Takemura<br />
SYMPOSIUM AND GENERAL SESSIONS:<br />
Each symposium may take about a half day and will<br />
consist of several oral presentations focused on some<br />
particular topic of <strong>radiolaria</strong>n research. Presentations<br />
which do not fall in the categories of proposed symposia<br />
will be included in general sessions. All the presentations<br />
should be made in English. Please indicate the category of<br />
your presentation in Information Sheet for Abstract. The<br />
following three symposia are proposed:<br />
Symposium A: Radiolarian survival, extinction and<br />
recovery across major geologic boundaries. Convener:<br />
ISHIGA, Hiroaki (Shimane University)<br />
Symposium B: Radiolarians and Orogenic Belts.<br />
Convener: MATSUOKA, Atsushi (Niigata University)
Radiolaria 14 Interrad VII<br />
Symposium C: Radiolarians as Environmental and<br />
Paleoenvironmental Proxy and Their Ecology. Convener:<br />
TAKAHASHI, Kozo (Hokkaido Tokai University)<br />
For further information about these symposia, please<br />
contact the conveners of each symposium or secretary.<br />
FIELD EXCURSIONS:<br />
The organizing committee is planning two preconference<br />
field excursions (I: Paleozoic, and II:<br />
Mesozoic) and one post-conference field excursion<br />
(Cenozoic). ¥ 6,000 or US$ 55 should be paid as a<br />
deposit for each excursion before June 1, 1994. Detailed<br />
information of field excursions is provided within an<br />
attached sheet.<br />
The pre-conference field excursion proposed by Dr.<br />
Irina POPOVA (Far East Geological Institute, 690022<br />
Vladivostok, Russia) has been canceled.<br />
REGISTRATION FEE:<br />
US$100 or ¥11,000.<br />
The registration fee and deposits for accommodation<br />
and field excursions must be sent before June 1, 1994.<br />
ACCOMMODATION:<br />
The Inter-University Seminar House of Kansai<br />
(IUSK) is a facility mainly for educational purposes of<br />
universities in Kansai Area. Therefore, all the rooms and<br />
facilities were made for student house. We have 100<br />
double rooms in IUSK. Except for the first day (20 Oct.),<br />
when another meeting will be held at IUSK, you can<br />
choose rooms for single or double use.<br />
All rooms include two single beds without bathroom.<br />
Single: US$110 or ¥ 12,000 per night Double: US$80 or<br />
¥ 9,000 per night These fees include meals from the<br />
supper of 20 Oct. to breakfast of 24 Oct. 20% of the total<br />
accommodation fee must be paid as a deposit before June<br />
1, 1994.<br />
PAYMENT:<br />
Payment of the registration fee as well as deposits for<br />
accommodation and field excursions must be sent to<br />
SUGANO, Kozo, Treasurer of InterRad VII, before June<br />
1, 1994. The payment should be made by POSTAL<br />
MONEY ORDER or BANK TRANSFER. Please<br />
do not send a bank check, because Japanese banks charges<br />
more than $20 commission. People in some countries,<br />
who cannot send payment by postal money order or bank<br />
transfer, should contact Treasurer or Secretary.<br />
The Accommodation Form enclosed with this circular<br />
must also be completed and sent to Treasurer before June<br />
1, 1994. Please do not send this form by Fax, because<br />
sometimes we cannot read your letters.<br />
Bank Account:<br />
Account name: INTERRAD Vll<br />
Account number: 2331387<br />
1-2-3 Hongo, Kashiwara,<br />
Osaka 582, JAPAN<br />
- 17 -<br />
Address of Treasurer:<br />
SUGANO, Kozo<br />
Division of Natural Science<br />
Bank: Daiwa Bank, Kashiwara Branch<br />
Osaka Kyoiku University<br />
Kashiwara, Osaka 582, JAPAN<br />
ABSTRACTS:<br />
Abstracts must be written in English and should not<br />
exceed one page including figures and tables, for both oral<br />
and poster presentations. Use standard A4 or US letter<br />
paper, and type single- to double-spaced. Because we use<br />
optical character reading (OCR) system for reproduction,<br />
we recommend use of courier 12 or Helvetica 12 fonts.<br />
[Example of abstract format]:<br />
MICHAEL JORDAN'S RETIREMENT AND<br />
ITS WORLDWIDE INFLUENCE ON<br />
RADIOLARIAN RESEARCH.<br />
B. Green* and S. Yehara**<br />
*) Department of Paleontology,<br />
Faculty of Psychics, Piltdown<br />
University, JAPAN<br />
**) 38-800 Ninten-do, Mario-cho,<br />
Sega 557, JAPAN<br />
Abstracts accompanied by completed Information<br />
Sheet must be sent before June l, 1994 to TAKEMURA,<br />
Atsushi, Secretary of InterRad VII. Do not send abstract<br />
and information sheet by fax.<br />
POSTERS:<br />
The size of individual posters is 1.0m X l.5m.<br />
PROCEEDINGS:<br />
We strongly encourage you to publish your papers in<br />
the Proceedings of InterRad VII. We plan to publish these<br />
Proceedings in (1) Marine Micropaleontology Special<br />
Volume and (2) one of the geological journals as a special<br />
volume.<br />
For the Marine Micropaleontology Special Volume<br />
appropriate papers include the following or closely related<br />
subjects: Paleoceanography, evolution, paleoecology,<br />
biology and paleobiology, biochronology,<br />
paleoclimatology, taphonomy, the systematic<br />
relationships of higher taxa, and micropaleontology which<br />
is used to solve fundamental geological and biological<br />
problems. Use of English language is requested. Other<br />
guidelines and publication policy will follow that of<br />
Marine Micropaleontology. More details will be available<br />
in the Third Circular.<br />
The manuscripts that do not fall in the above category<br />
will be published as a special volume in one of the<br />
geological journals. Submission date of the manuscripts:<br />
target date - 20 October, 1994. We request that those who
Interrad VII Radiolaria 14<br />
wish to publish their contributions bring the manuscript<br />
to the InterRad VII Conference. We plan to publish these<br />
promptly. Earlier submission will be welcomed. Inquiries<br />
should be directed to: TAKAHASHI, Kozo for Marine<br />
Micropaleontology Special Volume: and YAO, Akira for<br />
the special volume in one of the geological journals.<br />
FUNDING:<br />
We cannot fund any travel costs to and from Japan.<br />
Limited funding may be available for accommodation fee<br />
for those from developing countries or students. If your<br />
participation to the meeting absolutely depends on partial<br />
or complete funding or discount, please indicate in the<br />
Accommodation Form.<br />
TRAVEL:<br />
Osaka is the second largest city in Japan and the<br />
population of its metropolitan area (including Kobe) is<br />
more than 10 million. "Kansai" means the region around<br />
Kyoto and Osaka, including Kobe and Nara.<br />
The new international airport (Kansai International<br />
Airport, KIX) will open on 4 September, 1994, on a<br />
reclaimed island in Osaka Bay, located about 35 km<br />
southwest of downtown. All international flights, which<br />
will link Osaka to more than 30 countries, will arrive at<br />
and depart from KIX after opening. Another airport, Osaka<br />
International Airport (OSA), located about 12 km<br />
northwest of downtown, will become mostly a domestic<br />
one.<br />
Highways and two railway companies, Nankai Line<br />
and Japan Railways (JR) Hanwa Line, will connect the<br />
new airport (KIX) to downtown Osaka. Trains of Nankai<br />
Line go to Namba, the south downtown of Osaka city,<br />
and those of JR Hanwa Line go to Tennoji, Shin-Osaka<br />
and Kyoto Stations. Osaka City University is located on<br />
the east of Sugimoto-cho Station of JR Hanwa Line.<br />
Both the timetables and the prices of railroads have not<br />
been determined yet, but it will take less than I hour and<br />
will cost less than ¥ 1,500 (US$ 14) between KIX and<br />
Sugimoto-cho.<br />
Tokyo is about 500 km noxtheast of Osaka. New<br />
Tokyo International Airport (Narita, NRT) is situated at<br />
about 60 km east of downtown Tokyo. Airport limousine<br />
buses (90 minutes, ¥ 2,800, US$26) or JR trains (60<br />
minutes, about ¥ 2,900, US$27) connect NRT and Tokyo<br />
Station. Bullet trains (Tokaido-Shinkansen) are available<br />
from Tokyo Station to Shin-Osaka Station every l 0 to<br />
30 minutes from 6:00 to 20:45. It takes about 3 hours<br />
and costs about ¥ 13,500 (one way, US$123).<br />
Some of this information about travel may be<br />
changed in 1994. We will supply more detailed<br />
information in the last circular.<br />
DEADLINES:<br />
June 1, 1994 send to:<br />
Registration fee ........................................ Treasurer<br />
Deposit (20%) of accommodation fee ............ Treasurer<br />
¥ 6,000 or $55 for 1 excursion per person ..... Treasurer<br />
Abstracts ................................................. Secretary<br />
- 18 -<br />
The payments must be accompanied by completed<br />
Accommodation Forms. The Information Sheet must be<br />
enclosed with abstracts.<br />
INFORMATION:<br />
For further information, please contact TAKEMURA,<br />
Atsushi, Secretary, or other members of the organizing<br />
committee.<br />
ORGANIZING COMMITTEE:<br />
NAKASEKO, Kojiro, Honorary Chairperson: Kobe<br />
Yamate Women's College, Kobe 650, Japan.<br />
YAO, Akira, Chairperson: Department of Geosciences,<br />
Faculty of Science, Osaka City University, Osaka 558,<br />
JAPAN, Phone: 81-6-605-2604, Fax: 81-6-605-2604 or<br />
2522, E-mail: hl682@ocugw.cc.osaka-cu.ac jp<br />
AITA, Yoshiaki, Cenozoic Radiolaria: Department of<br />
Geology, Faculty of General Education, Utsunomiya<br />
University, Utsunomiya 321, JAPAN, Phone: 81-286-36-<br />
1515 ext. 577, Fax: 81-286-35-3171<br />
ISHIGA, Hiroaki, Paleozoic Radiolaria: Department<br />
of Geology, Shimane University, Matsue 690, JAPAN,<br />
Phone: 81-852-32-6459, Fax: 81-852-32-6469, E-mail:<br />
G01483C@sinet.ad.jp<br />
KITO, Norio: Institute of Earth Science, Hokkaido<br />
University of Education, Hakodate 040, JAPAN, Phone:<br />
81-138-41-1121,Fax: 81-138-42-3982<br />
MATSUOKA, Atsushi, Mesozoic Radiolaria:<br />
College of General Education, Niigata University, Niigata<br />
950-21, JAPAN, Phone: 81-25-262-6376, Fax: 81-25-<br />
262-7278<br />
NISHIMURA, Akiko: 3212 Satoyamabe,<br />
Matsumoto, Nagano 390-02, JAPAN, Phone: 81 -263-<br />
34-0497<br />
SAKAI, Toyosaburo: Department of Geology,<br />
Faculty of General Education, Utsunomiya University,<br />
Utsunomiya 321, JAPAN, Phone: 81-286-36-1515 ext.<br />
602, Fax: 81-286-35-3171<br />
SASHIDA, Katsuo: Institute of Geoscience,<br />
University of Tsukuba, Tsukuba, Ibaraki 305, JAPAN,<br />
Phone: 81 -298-53-4303, Fax: 81 -298-51 -9764<br />
SUGANO, Kozo, Treasurer: Division of Natural<br />
Science, Osaka Kyoiku University, Kashiwara, Osaka<br />
582, JAPAN, Phone: 81-729-76-3211, ext. 4320, Fax:<br />
81-729-76-3273<br />
TAKAHASHI, Kozo, Recent/Living Radiolaria:<br />
Hokkaido Tokai University, Minami-ku, Sapporo 005,<br />
JAPAN, Phone: 81 - 11 -571 -5112 ext. 615, Fax: 81 -<br />
11 -571 -7879<br />
TAKEMURA, Atsushi, Secretary: Geoscience<br />
Institute, Hyogo University of Teacher Education,<br />
Yashiro-cho, Kato-gun, Hyogo 673-14, JAPAN, Phone:<br />
81-795-44-2206, Fax: 81-795-44-2189.
Radiolaria 14 Interrad VII<br />
FIELD EXCURSIONS<br />
InterRad VII Osaka, 1994<br />
Pre-Conference Field Excursion I (Paleozoic)<br />
Late Paleozoic bedded cherts and Permian/Triassic<br />
boundary in the Tanba Terrane, Southwest Japan<br />
Date: 18 Oct. (Tue) through 20 Oct. (Thu), 1994.<br />
Excursion starts in or around Osaka and ends at IUSK<br />
(Inter-University Seminar House of Kansai, the place of<br />
conference).<br />
Organizer: ISHIGA, Hiroaki (Shimane<br />
University)<br />
This excursion has been organized to provide an<br />
overview of the Meso-Paleozoic bedded chert sequence<br />
embedded in the Jurassic accretionary rocks of Southwest<br />
Japan, especially in the Sasayama area situated 25 km<br />
north of the IUSK. It starts in Upper Carboniferous<br />
oceanic basalt/red bedded cherts. Progressively younger<br />
successions of the bedded chert sequence will be visited in<br />
and around the area with an emphasis on <strong>radiolaria</strong>n and<br />
conodont biostratigraphy, and geochemical and stable<br />
isotopic studies. Attention will focuse on analysis of<br />
rhythmicity in the bedded cherts which correlates with<br />
global change in oceanic conditions. Particular emphasis<br />
will be directed to the Permian/Triassic boundary event<br />
recorded in the bedded chert sequence.<br />
Provisional schedule<br />
18 October (Tue): Assemble at Kansai International<br />
Airport (KIX) or Osaka City University (OCU) at<br />
9:00 AM. Transportation is by courtesy minibus<br />
during this excursion. Travel to Sasayama (about 2.5<br />
hours drive) to examine Carboniferous greenstone and<br />
red bedded chert sequence and the Permian/Triassic<br />
bedded cherts crossing the boundary. Stay at Sasayama<br />
(ryokan=Japanese inn or hotel).<br />
19 October (Wed): Visit the northem part of the Sasayama<br />
area to examine lithologic change of the Upper<br />
Permian bedded chert to P/T boundary beds (claystones<br />
and organic black mudstones) in detail. Upper Triassic<br />
chert sequence representing clear rhythmicity. Travel<br />
to Kyoto to stay and sightsee in the evening.<br />
20 October (Thu): Visit Hozukyo gorge, west of Kyoto<br />
City, to examine Triassic conodont biostratigraphy<br />
and rhythmicity of Triassic to Early Jurassic bedded<br />
cherts. Travel to IUSK in the afternoon (about 2 hours<br />
drive from Hozukyo). Fee: ¥ 30,000 (including<br />
accommodation, transportation and 6 meals).<br />
Pre-Conference Field Excursion 11 (Mesozoic)<br />
Triassic-Jurassic <strong>radiolaria</strong>n-bearing sequences in the Mino<br />
Terrane, Central Japan<br />
Date: 19 Oct. (Wed) through 20 Oct. (Thu), 1994.<br />
Excursion starts at a hotel near JR Shin-Osaka<br />
Station and ends at IUSK (the Inter-University Seminar<br />
House of Kansai, the place of conference).<br />
Organizer: MATSUOKA, Atsushi (Niigata<br />
University)<br />
- 19 -<br />
The Inuyama area is about 25 km to the north of<br />
Nagoya City. This field excursion concentrates on<br />
continuous Triassic-Jurassic sequences composed of Early<br />
Triassic claystone, Middle Triassic to Early Jurassic<br />
bedded chert, Middle Jurassic siliceous mudstone, and<br />
Middle Jurassic clastic rocks. Extensive biostratigraphic<br />
studies on Triassic-Jurassic <strong>radiolaria</strong> and Triassic<br />
conodonts have been carried out on these sequences.<br />
Participants will be able to collect rock samples<br />
containing <strong>radiolaria</strong>n faunas of Triassic-Jurassic age.<br />
Provisional schedule<br />
19 October (Wed): Assemble at a hotel near JR Shin-<br />
Osaka Station at 7:30 AM. Travel to Inuyama by bus and<br />
spend a full day along the river bank of the Kiso River.<br />
Stay at Inuyama.<br />
20 October (Thu): Spend a half day in the Inuyama area<br />
for further observation or for a visit to Inuyama Castle,<br />
and travel to IUSK.<br />
Fee: ¥ 30,000 including accommodation on 18 October<br />
(Tue). Note: All participants are recommended to stay at a<br />
hotel near JR Shin-Osaka Station on 18 October. Further<br />
information will be given in the third circular.<br />
Post-Conference Field Excursion (Cenozoic)<br />
Neogene siliceous microfossil-bearing sequences of the<br />
Northern Kanto District<br />
Date: 25 Oct. (Tue) through 27 Oct. (Thu), 1994.<br />
Excursion starts and ends at JR Utsunomiya Station.<br />
Organizers: SAKAI, Toyosaburo and AITA,<br />
Yoshiaki (Utsunomiya University)<br />
This field trip will focus on <strong>radiolaria</strong>n paleoecology<br />
in the biosiliceous facies of the Upper Miocene Arakawa<br />
Group. The upper part of the Group contains abundant<br />
<strong>radiolaria</strong>ns and diatoms in sandy mudstones and<br />
diatomaceous mudstones of the Oogane, Tanokura, and<br />
Irieno Formations. A sudden marked increase in the<br />
abundance of Cyrtocapsella japonica (Nakaseko) in this<br />
section represents a major paleoceanographic event which<br />
can be traced throughout NE Japan. This horizon is<br />
within the Didymocyrtis antepenultima Zone and<br />
probably reflects a regional cooling event. We will also<br />
look at other aspects of the geology of the Northern<br />
Kanto District, notably the underlying Nakagawa Group,<br />
which is composed of andesite volcanic breccias, and the<br />
Pleistocene Shiobara Group, which mainly consists of<br />
lake deposits including diatom-rich and plant fossilbearing<br />
varve sediments at Shiobara. The second day will<br />
include a visit to a traditional pottery at Koisago. Both<br />
nights will be spent sampling the pleasures of a<br />
traditional Japanese onsen (hot spa inn). For those<br />
wishing to take part, an optional addition of an extra day<br />
(28 Oct.) is planned to visit the beautiful shrines and<br />
scenery at Nikko.<br />
Provisional schedule<br />
25 October (Tue): Assemble at JR Utsunomiya Station at<br />
17:00. Travel by courtesy minibus to Koisago-Mitama<br />
Onsen (hot spa) at Bato about 40 km East of Utsunomiya<br />
City. Stay at Seizanso (Japanese onsen).
Interrad VII Radiolaria 14<br />
26 October (Wed): Spend a full day for examination of<br />
geology of the Arakawa Group and the underlying<br />
Nakagawa Group. Travel by rented minibus for remainder<br />
of trip. Stay at Seizanso.<br />
27 October (Thu): Visit Koisago Pottery. Travel to<br />
Shiobara and look at the Pleistocene lake deposits<br />
including diatomaceous varve sediments. Visits Museum<br />
of Fossil Leaves. Ends at JR Utsunomiya Station at<br />
15:30.<br />
Fee: ¥ 30,000 (not including travel from Osaka to<br />
Utsunomiya).<br />
Travel to Utsunomiya: It takes three hours from Osaka to<br />
Tokyo by Tokaido Shinkansen (bullet train), and 50<br />
- 20 -<br />
minutes by Tohoku Shinkansen (bullet train) from Tokyo<br />
to Utsunomiya. Cost is ca. ¥ 17,000.<br />
28 October (Fri): Optional tour of Nikko. Visit beautiful<br />
shrines and scenery at Nikko. Ends at JR<br />
Utsunomiya Station evening. Travel by a minibus.<br />
Note: This Nikko tour is available for all conference<br />
participants not only those attending the field trip.<br />
Fee: ¥ 15,000 (including accommodation on 27 Oct. and<br />
travel expenses).<br />
New announcement from the Secretary of INTERRAD Vll, Osaka.<br />
The InterRad Vll Conference will be held near Osaka,<br />
Japan, 20 to 24<br />
October, 1994. We, the organizing committee, had mailed<br />
the 1 st Circular last June, 1993 and more than 150<br />
people from 25 countries have responded the 1st Circular.<br />
The details are follows (until 1994.3.1):<br />
Yes Probably No<br />
Attend 100 55 6<br />
Oral 72 34 30<br />
Poster 37 30 29<br />
Excursion Paleozoic 28 11 47<br />
Excursion Mesozoic 38 42 31<br />
Excursion Cenozoic 6 25 39<br />
Countries Yes Probably No<br />
Albania 1<br />
Argentine 1<br />
Australia 2 1<br />
Bangladesh 5<br />
Canada 2<br />
China 3 2<br />
France 3 1<br />
Germany 4 2<br />
Hungary 1<br />
India 2<br />
Indonesia 1<br />
Italy 5 1 1<br />
Israel 1<br />
Japan 43 16 1<br />
Mexico 1<br />
Netherlands 1<br />
New Zealand 2<br />
Poland 1<br />
Atsushi Takemura<br />
Atsushi Takemura<br />
Russia 15 11<br />
Slovenia 1<br />
Swittzerland 3 2<br />
Taiwan 3<br />
Ukraine 1<br />
UK 1 2<br />
USA 6 8<br />
We have already sent the 2nd Circular in this January.<br />
Unfortunately, the pre-conference excursion in<br />
Vladivostok has been cancelled. The deadlines of abstract<br />
and payment of fees are June 1, 1994. If you have an<br />
interest to InterRad VII and does not receive the 2nd<br />
Circular, please contact the secretary of the following<br />
address:<br />
Secretary of InterRad VII<br />
Dr. Atsushi TAKEMURA<br />
Geoscience Institute<br />
Hyogo University of Teacher Education<br />
Yashiro-cho, Kato-gun<br />
673-14 Hyogo JAPAN<br />
Any suggestions or requests are also welcome. See you<br />
soon.<br />
Atsushi Takemura
Radiolaria 14 Meetings<br />
1994<br />
• 29 May-1 June 1994<br />
Oslo, Norway. - Glacial Cycles at High<br />
Latitudes—the: effect on the physical<br />
environment. Information: GCHL<br />
Organizing Committee, Department of<br />
Geology, PO Box 1047. Blindern. 0316<br />
Oslo. Norway.<br />
• 6-7 June 1994<br />
Cambridge, U.K. - Weddell Sea Tectonics<br />
and Gondwana Breakup. Information:<br />
British Antarctic Survey, High Cross<br />
Madingley road, Cambridge CB3 OET G-<br />
Bj Tel. 44-22-361188; Fax 44-22-<br />
362616<br />
• 12-15 June 1994<br />
Denver, U.S.A. - AAPG: annual meeting.<br />
Information: MPG, Box 979, Tulsa,<br />
Oklahoma, U.S.A<br />
• 4-8 July. 1994<br />
Sydney, Australia. - History of the<br />
geological Sciences in the Pacific<br />
region. Symposium et excursion.<br />
Information: 9th INHI GEO<br />
symposium, c/o Earth Resources<br />
Foundation, Department of Geology,<br />
University of Sydney, New South<br />
Wales, Australie 2006. Tel. 61-25-<br />
526136. Fax 61-25-526058.<br />
• 5-8 July.1994<br />
Berkeley, U.S.A. - Forams'94.<br />
Information: Forams'94, Museum of<br />
Paleontology, University of<br />
California, Berkeley, CA 94720,<br />
U.S.A.<br />
• 6-10 July 1994<br />
Vienna, Austria. - European Association<br />
of Petroleum geologists. 6th Annual<br />
Conference. Information: Evert Van der<br />
Gaag, P.O. Box 298, 3700 AG Zeist,<br />
Pays-Bas. Tel. 31-3 40456997. Fax<br />
31-3-40462640.<br />
• 7-9 July 1994<br />
Milano Italy. - 2nd Workshop EPA<br />
Radiation in the History of Life.<br />
Information: Giovanni Pinna Museo di<br />
Storia Naturale di Milano, Corso<br />
Venezia 55, 20121 Milano, Italy, Tel:<br />
39-2-76799870, Fax: 39-2-76022287.<br />
•16-20 July 1994<br />
Angers, France. - 12ème Colloque<br />
africain de micropaléontologie et 2ème<br />
colloque de stratigraphie et<br />
International Meetings of interest to Paleontologists<br />
paléogeographie de l'Atlantique sud.<br />
Information: J.-P. Debenay,<br />
Laboratoire de Géologie, 2, bld<br />
Lavoisier 49045 Angers, Cedex<br />
France. Tei. 33-41 73 53 82. Fax 33-<br />
41735352.<br />
• 15-18 Agust 1994<br />
Bremen, Germany. - The South Atlantic:<br />
present and past circulation.<br />
Information: Barbara Donner,<br />
Fachbereich geowissenschaften der<br />
Universität, Postfach 330440, D-<br />
28334 Bremen, Germany. Tel. 49-<br />
2212181; Fax 49-4212183116.<br />
• 21-24 Agust 1994<br />
Kuala Lumpur, Malaysia. - AAPG,<br />
international meeting. Information:<br />
AAPG, Box 979, Tulsa, Okla 74 101,<br />
U.S.A. Tel. 918-584 2555. Fax 918-<br />
584 0469.<br />
• 28-31 Agust 1994<br />
Guiyang Guizhou, China. - Permian<br />
stratigraphy, environments and<br />
ressources. Intern. symposium.<br />
Information: Wang Xiang-dong, secr.<br />
ISP-94, Lab. Paleobiology, Nanjing<br />
Inst. of Geology & Paleontology Chi-<br />
Ming-Ssu, Nan-jing 210008, Chine.<br />
Tel. 86-25-714443. Fax 86-25-<br />
712207.<br />
• 5-8 September 1994<br />
Plymouth, U.K. - Biotic Recoveries from<br />
Mass Extinctions, IGCP Project 335,<br />
Plymouth, United Kingdom.<br />
Information: Malcom B. Hart, Dept. of<br />
Geological Sciences, University of<br />
Plymouth, Drake Circus, Plymouth,<br />
Devon PlA 8AA, UK, fax 44-745-233-<br />
117; or Douglas H. Erwin, Dept. of<br />
Paleobiology, NHB-121, Smithsonian<br />
Institution, Washington, D.C. 20560,<br />
U.S.A. Tel: 1-202-3572053.; fax: 1-<br />
202-7862832.<br />
• 5-9 September 1994<br />
Magadan, Russia. - International<br />
Conference on Arctic Margins, (ICAM<br />
'94), Magadan, Russia. Information:<br />
Kirill V. Simakov, North East Science<br />
Center, Russian Academy of Sciences,<br />
16 Portovaya St., Magadan, Russia<br />
685000, (907) 474-7219 (USA) or 74-<br />
13-2230953 (Russia); or Dennis K<br />
Thurston, Minerals Management<br />
Service, 949 E. 36th Ave., Anchorage,<br />
AK 99508-4302, (907) 271-6545, fax<br />
907-271-6565.<br />
- 21 -<br />
• 21-22 September 1994<br />
London, U.K. - The North Atlantic and<br />
the global carbon cycle. Organized by<br />
Professor G. Eglinton, Dr H. Elderfield,<br />
Dr M. Whitfield, and Professor P.L.B.<br />
Williams. Information: The Scientific<br />
Meetings Secretary, The Royal<br />
Society, 6 Carlton House Terrace,<br />
London SWlY 5AG. Tel: 44-71-<br />
8395561 ext 278; fax: 44-719302170<br />
• 12-13 October 1994<br />
London U.K. - The Arctic and<br />
environmental change. Organized by<br />
Dr J. Dowdeswell, Dr N. Owens,<br />
Profesor A.N. Schofield and Dr P.<br />
Wadhams. Information: The Scientific<br />
Meetings Secretary, The Royal<br />
Society, 6 Carlton House Terrace,<br />
London SWlY 5AG. Tel: 44-71-<br />
8395561 ext 278; fax: 44-71-9302170<br />
• 15-17 October 1994<br />
Kingston, Jamaica. - A Symposium on<br />
Geological and Biological Evolution<br />
of the Caribbean Region, A 60th<br />
Birthday Celebration in Honor of<br />
Professor Edward Robinson,<br />
University of the West Indies,<br />
Kingston 7, Jamaica. Information:<br />
Drs. Trevor Jackson and Stephen<br />
Donovan, Department of Geology,<br />
University of the West Indies,<br />
Kingston 7, Jamaica. Tel: 809-L 927-<br />
2728, Fax: 809-927-1640.<br />
• 15-26 October 1994<br />
La Plata, Argentina. - 4th International<br />
Congress on Jurassic Stratigraphy and<br />
Geology, Mendoza and Neuquen<br />
provinces of Argentina. Information:<br />
Dr. A.C. Riccardi C.C. 886, 1900 La<br />
Plata, Argentina.<br />
• 20-24 October. 1994<br />
Osaka, Japan. - Interrad VII. 7th meet.<br />
International Association of<br />
Radiolarian Paleontologists.<br />
Information: A. Takemura, Geoscience<br />
Institut Hyogo Univ. of Teacher<br />
Education, Yashiro-cho, Kato-gun,<br />
Hyogo 673-14 Japon. Tel. 81/795 44<br />
2206; Fax 81/795-442189<br />
• 24-27 October. 1994<br />
Seattle, U.S.A. Geological Society of<br />
America. Ann. meet. Information: Jean<br />
Kinney, GSA Headquarters P.O. Box<br />
9140, 3300 Penrose Place Boulder CO<br />
30301, U.S.A.. Tel. 1/303 447 2020.
Meetings Radiolaria 14<br />
• 29 November-7 December 1994<br />
Rabat, Morocco. - International<br />
Geological Correlation Program,<br />
Project 351: Early Palaeozoic<br />
Evolution in NW Gondwana, Morocco.<br />
Information: Dr N. Hamoumi,<br />
Department of Geology, Faculty of<br />
Sciences of Rabat, BP 1226, RP Rabat,<br />
Morocco. Tel: 212-7-771957; fax:<br />
212-7-774261; Telex 36607 M.<br />
• 3-10 December 1994<br />
St-Petersburg, Russia. - First<br />
International Symposium<br />
Biostratigraphy of Oil and Gas Basins,<br />
Saint-Petersburg, Russia. Information:<br />
VNIGRI, Liteiny 39, St-Petersburg,<br />
191104 Russia, Tel: (78)12-2757145,<br />
272-3677, Fax: (78) 12-2737387.<br />
• 7-8 December 1994,<br />
London, U.K. - Tectonic Evolution of<br />
Southeast Asia, London, UK.<br />
Information: Robert Hall, Geological<br />
Sciences, University College, Gower<br />
St., London WC1E 6BT, UK, Tel: 44-<br />
784-443592, fax 44-71-387-1612, Email<br />
(Internet): robert.hall@ucl.ac.uk.<br />
1995<br />
• 5-8 March 1995<br />
Houston, U.S.A. - American Association<br />
of Petroleum Geologists. Ann. meet.<br />
Information: AAPG conv. Dpt., P.O.<br />
Box 979 Tulsa OK 74101, U.S.A. Tel.<br />
1-918-5842555.<br />
• 12-16 June 1995<br />
Las Vegas, U.S.A. - 7th International<br />
Symposium on the Ordovician System,<br />
Las Vegas, Nevada. Information:<br />
Margaret N. Rees, Dept. of Geoscience,<br />
Univ. of Nevada at Las Vegas, Las<br />
Vegas, NV 89154. (702) 739-3262.<br />
• 1-3 July 1995<br />
Philadelphia, U.S.A. - Third<br />
International Paleoecology Congress.<br />
University of Pennsylvania,<br />
Philadelphia, PA. Information: G.<br />
Boyajian, Dept. of Geology, Univ.<br />
Penn., 240 South 33rd St.,<br />
Philadelphia, PA 19104.<br />
• 28 August - 2 September 1995<br />
Sosnowiec, Poland. - XIII International<br />
Congress on Carboniferous-Permian<br />
Krakow, Poland. Information: XIII<br />
ICC-P Secretary-General Prof. Dr.<br />
Sonia Dybova-Jachowicz, Panstwowy<br />
Instytut Geologiczny Oddzial<br />
Gornoslaski, I Krolowej Jadwigi, 41-<br />
200 Sosnowiec, Poland, Tel: 48-32 66<br />
20 36/38, Fax: 48-32 66 5S 22.<br />
• 8-14 September 1995<br />
Brussels, Belgium. - 2nd International<br />
Symposium on Cretaceous Stage<br />
Boundaries. Information: Dr. A. V.<br />
Dhondt, Institut royal des Sciences<br />
Naturelles de Belgique-Koninklÿk<br />
Belgisch Institut voor<br />
Natuunvetenschappen, Vautierstraat<br />
29, B-1040 Brussels, Belgium Fax: 32-<br />
2-6464433, (Tel.: 32-2-6274492.<br />
• September 1995<br />
Bucarest, Roumania. - 10th Congress<br />
Regional Committee in Mediterranean<br />
Neogene Stratiraphy. Information:<br />
Florian Marinescu, RCMNS, Instiute of<br />
Geology & Geophysics, 1 caransebes<br />
- 22 -<br />
st., RO 79678 Bucarest 32, Roumanie.<br />
Fax 40/13128444. Telex 12286 IGRR<br />
• 10-14 October. 1995<br />
Halifax, New Scotia, Canada. - Fifth<br />
International Conference on<br />
Paleoceanography. Information Larry<br />
Mayer or Frank Rack, Ocean Mapping<br />
Group. Dept. of Surveying<br />
Engineering, P.O. Box 4400<br />
Fredericton, NB Canada E3B 5A3;<br />
Internet: larry@atlantic.cs.unb.ca or<br />
rack@atlantic.cs.unb.ca. Or: David<br />
Piper, Atlantic Geoscience Centre,<br />
Bedford Institute of Oceanographie, PO<br />
Box 1006, Dartmouth, NS Canada B2Y<br />
4A2, Internet: piper@agcrr.bio.ns.ca<br />
• 22-25 October. 1995<br />
Le Caire, Egypte. - International<br />
conference of AAPG. Information:<br />
American Association of Petroleum<br />
Geologists, P.O. Box 979, Tulsa Okl<br />
74101, U.S.A.<br />
• 6-9 November 1995<br />
New-Orleans, U.S.A.- Geological<br />
Society of America. Ann. meet.<br />
Information: Jean Kinney, GSA<br />
Headquarters, Box 9140, 3300 Penrose<br />
Place, Boulder, CO 80301, U.S.A. Tel,<br />
1-303 447 2020.<br />
1996<br />
• 4-14 August 1996<br />
Beijing, China. - 30th International<br />
Geological Congress. Information:<br />
Secretariat bureau International<br />
Geological Congress; PO box 823,<br />
Beijing 100037, China.
Radiolaria 14 Bibliography - 1989<br />
Bibliography 1989-1994<br />
Luis O'Dogherty<br />
Since Radiolaria 13, almost four years of bibliographical silence have passed. This compilation intends to cover this<br />
time span. I am perfectly aware of the impossibility to compile a complete bibliography including all existing references.<br />
Therefore, you are kindly requested to notify any mistake or omitted reference. In this place, I wish to express my most<br />
sincere thanks to all those colleagues that sending their articles had collaborated and made possible this bibliography. Thanks<br />
to everybody.<br />
Adachi, M. 1989. Discovery of Late Triassic <strong>radiolaria</strong>ns<br />
from the Ino Formation, central Shikoku. J. geol. Soc. Japan,<br />
95/1, 81-83. (in Japanese)<br />
Adams, K.E. & Siok, J.P. 1989. Permian stratigraphy<br />
in the Atigun Gorge area; a transition between the Echooka<br />
and Siksikpuk formations. In: Dalton Highway, Yukon River<br />
to Prudhoe Bay, Alaska; bedrock geology of the eastern<br />
Koyukuk Basin, central Brooks Range, andeastcentral Arctic<br />
Slope. Guidebook. (Mull, C.G. et al., Eds.), vol. 7. Alaska<br />
Division of geological and geophysical Surveys, Report, pp.<br />
267-276.<br />
Alexandrovich, J.M. 1989. Radiolarian biostratigraphy<br />
of ODP Leg 111, Site 677, eastern equatoria6l Pacific, Late<br />
Miocene through Pleistocene. In: Proceedings of the Ocean<br />
Drilling Program, Scientific Results. (Becker, K., Sakai, H. et<br />
al., Eds.), vol. 111. College Station, TX (Ocean Drilling<br />
Program), pp. 245-262.<br />
Well-preserved late Miocene through Pleistocene age<br />
<strong>radiolaria</strong>n assemblages were recovered during ODP Leg 111 at Site<br />
677, on the southern flank of the Costa Rica Rift in the eastern<br />
equatorial Pacific. Radiolarian "event" biostratigraphy (first and last<br />
morphotypic appearances) was established for Holes 677A and<br />
677B using 21 species yielding 24 reliable datum levels. The cold<br />
upwelling waters above this site have prevented many typical<br />
tropical Pacific stratigraphic <strong>radiolaria</strong>ns from being useful age<br />
indicators. Biostratigraphic datum levels were assigned absolute<br />
ages based on previous work and were used to date the cores.<br />
Sedimentation rates varied from 3.7 cm/1000 yr. in the late<br />
Pleistocene to 6.0 cm/1000 yr. in the late Miocene. The age of the<br />
oldest sediments at this site is estimated as 5.89-6.37 Ma, which<br />
indicates that Site 677 is between magnetic anomalies 3A and 4. A<br />
total of 67 taxa were assessed for stratigraphic relevance at this<br />
site and are listed in the Appendix. One previously unknown Pliocene<br />
<strong>radiolaria</strong>n stratigraphic indicator, Botryostrobus euporus<br />
(Ehrenberg), is identified.<br />
Alexandrovich, J.M. & Hays, J.D. 1989. Highresolution<br />
stratigraphic correlation of ODP Leg 111 Holes<br />
677A and 677B and DSDP Leg 69 Hole 504. In: Proceedings<br />
of the Ocean Drilling Program, Scientific Results. (Becker,<br />
K., Sakai, H. et al., Eds.), vol. 111. College Station, TX<br />
(Ocean Drilling Program), pp. 263-276.<br />
The recovery of continuous sedimentary sequences has been<br />
and is a high-priority goal of the Ocean Drilling Program, yet its<br />
success has not been determined. We test the stratigraphic<br />
continuity of continuously cored sequences from ODP Leg 111 Holes<br />
677A and 677B and DSDP Leg 69 Hole 504. The two holes at Site<br />
677 and Hole 504 are correlated using high-resolution<br />
biostratigraphy, tephra stratigraphy, and time series of opaline silica<br />
and calcium carbonate. The correlation coefficient between the time<br />
series is maximized through an inverse correlation procedure.<br />
Changes in slope of the mapping function that relates the two<br />
sections indicate gaps or changes in the accumulation rate between<br />
sections. We assume as a first approximation that the sedimentary<br />
sequences are identical in each hole, given their close proximity.<br />
Slope changes of the mapping functions therefore result from errors<br />
introduced by coring. This assumption is justified by the fact that<br />
most mapping function slope changes occur at core breaks. Having<br />
identified missing sections in one site, it is possible to fill these<br />
gaps with the appropriate section from the adjacent site, thereby<br />
improving continuity. This is possible only where the sediment gaps<br />
identified at core breaks in one hole do not correspond to core break<br />
levels in the other hole. Results show that in the upper 100 m of the<br />
stratigraphic column, 3.1°70 and 4.6°70 were unsampled in Holes<br />
1989<br />
- 23 -<br />
677A and 677B, respectively, and 15°70 of the Pliocene portion of<br />
Hole 504 was not sampled by the hydraulic piston corer. This<br />
indicates that even in relatively calm seas, double or triple coring is<br />
required in order to ensure that gaps and doubly sampled intervals of<br />
the stratigraphic column which occur at core breaks are recognized<br />
and sampled at least once.<br />
Anderson, O.R. 1989. Some observations of feeding<br />
behavior, growth, and test particlemorphology of a silicasecreting<br />
testae Amoeba Netzelia tuberculata (Wallich)<br />
(Rhizopoda, Testacea) grown in laboratory culture. Arch.<br />
Protistenkunde, 137, 211-221.<br />
Netzelia tuberculata (WALLICH) fed with Iyophilized yeast in<br />
laboratory culture grows more rapidly (mean doubling time = 1.7 d)<br />
and produces siliceous test particles that are more smooth,<br />
spheroidal and regularly arranged than those fed with Spirogyra<br />
(mean doubling time = 3 1 d). The change in test particle morphology<br />
is observable during test secretion of the daughter cell in the first<br />
generation after transfer into a yeast medium. Successive<br />
generations exhibit increasingly more smooth and regularly arranged<br />
spheroidal test particles. N. tuberculata grown in a medium<br />
containing only soluble silicate (21 µM sodium silicate) reproduced<br />
and secreted siliceous test particles. Hence, a particulate source of<br />
silicate is not necessary for test particle synthesis. These results<br />
give further evidence of the ecophenotypic variation in test particle<br />
morphology of Netzelia tuberculata, in this case induced by<br />
variations in kind of food, and suggest that additional research is<br />
warranted on the cellular processes that determine the morphology<br />
of biomineralized products in these testate amoebae.<br />
Anderson, O.R., Bennett, P. & Bryan, M. 1989a.<br />
Experimental and observational studies of <strong>radiolaria</strong>n<br />
physiological ecology: 1. Growth, abundance and opal<br />
productivity of the spongiose <strong>radiolaria</strong>n Spongaster tetras<br />
tetras. Mar. Micropaleontol., 14/4, 257-266.<br />
The mean growth, longevity and percent of S. tetras tetras<br />
producing swarmers in laboratory-cultures were examined as a<br />
function of variations in water temperature, salinity and the<br />
intensity of illumination. Radiolaria were grown as individuals in<br />
optically clear glass vials maintained in environmentally controlled<br />
water baths and observed daily by light microscopy. The optimum<br />
growth and longevity occurred at moderately warmer temperatures<br />
and higher salinities (e.g. 27.5°C and 40‰ salinity) where maximum<br />
survival was 23 days compared to 4 days at a temperature of 21°C<br />
and 30‰ salinity. At higher temperatures of 33°C and 36°C, the<br />
maximum longevity was 2 and zero days respectively. Light was<br />
required for production of reproductive swarmers, but not for<br />
growth. At temperatures near or below 15°C, the axopodia became<br />
aggregated together or remained permanently withdrawn<br />
incumbering food gathering. Few individuals produced reproductive<br />
swarmers at 15°C and none produced swarmers at a temperature of<br />
10°C. These data indicate that S. tetras tetras may be restricted to<br />
warmer temperature water masses with an upper limit near 31°C.<br />
They survive better with higher salinity and warmer water (c. 28°C).<br />
Cold water and particularly dark conditions that occur at great<br />
depth, may not support large populations of S. tetras tetras since<br />
swarmer release is inhibited and, among other factors, food<br />
gathering is suppressed due to axopodial impairment.<br />
Anderson, O.R., Bennett, P., Angel, D. & Bryan,<br />
M. 1989b. Experimental and observational studies of<br />
<strong>radiolaria</strong>n physiological ecology: 2. Trophic activity and<br />
symbiont primary productivity of Spongaster tetras tetras<br />
with comparative data on predatory activity of some<br />
Nassellarida. Mar. Micropaleontol., 14/4, 267-273.
Bibliography - 1989 Radiolaria 14<br />
The prey of Spongaster tetras tetras, determined by<br />
transmission electron microscopic examination of ultrathin sections<br />
through food and digestive vacuoles, was predominantly<br />
picoplankton (1 to 3 µm, largely monerans) and only occasional<br />
vacuoles contained masses of larger digested organic matter. By<br />
contrast, Nassellarian specimens collected in the same location and<br />
fixed and examined identically contained nanoplankton prey (5-10<br />
µm) including small phytoplankton cells. The differences in prey may<br />
reduce competition for nutritional resources and account for the coexistence<br />
of these two groups of <strong>radiolaria</strong> in the same water mass.<br />
The primary productivity of the symbionts in intact S. tetras tetras<br />
was assessed at varying light levels to more fully document<br />
potential sources of carbon compounds for nutrition. Thirty-five µg<br />
of carbon were fixed per <strong>radiolaria</strong>n per hour at an intensity as low<br />
as 20 µE/ m 2 /s which is approximately one-third the maximum<br />
productivity in the intensity range of 170 to 260 µE/m 2 /s. The<br />
mean abundance of S. tetras tetras, density of potential prey, and<br />
physico-chemical characteristics of the water are presented for<br />
early spring (March-April), mid-summer (June and July), and late<br />
summer (August). The mean density of S. tetras tetras varied from<br />
c. 12 individuals/m 3 during the low productivity periods (spring and<br />
late summer) to 37.8 individuals/m 3 in July. The concentration of<br />
cyanobacteria was at a peak during July while larger autotrophic<br />
plankton was at a minimum further suggesting that cyanobacteria<br />
can be a significant food source for S. tetras tetras.<br />
Anderson, O.R., Bennett, P. & Bryan, M. 1989c.<br />
Experimental and observational studies of <strong>radiolaria</strong>n<br />
physiological ecology: 3. Effects of temperature, salinity and<br />
light intensity on the growth and survival of Spongaster<br />
tetras tetras maintained in laboratory culture. Mar.<br />
Micropaleontol., 14/4, 275-282.<br />
Stages of growth of Spongaster tetras tetras were observed<br />
using scanning electron microscopy. The earliest stage with a<br />
diagonal of about 75 to 100 µm is a biconvex, nearly lens-shaped,<br />
tabular structure. Subsequent growth by accretion of silica at the<br />
periphery produces a more quadrangular tabular skeleton that<br />
gradually increases in size by growth largely at the perimeter. The<br />
corners of the tabular skeleton at maturity are somewhat lobed due<br />
to the large quantities of silica deposited there during the later<br />
stages of development. Conspicuously larger pores occur in the<br />
surface of the skeleton at the four corners where the lobes are<br />
formed. Peripheral spines and a loose patagium of siliceous<br />
spongiose matter cover the surface of the skeleton at maturity (<br />
diagonal c. 300 to 400 µm ) . Based on a sample of skeletons of<br />
varying size collected in plankton tows near Barbados, a<br />
mathematical equation was derived relating mean weight of the<br />
skeleton of different maturational stages to the linear dimension in<br />
µm of the diagonal. This equation was used to estimate the amount<br />
of silica deposited per day in culture. It can also be used to estimate<br />
the amount of silica in samples of skeletons obtained from sediment<br />
cores, sediment traps or plankton tows that have been cleaned and<br />
prepared for observation with a light microscope. Based on this<br />
equation, the mean weight of silica deposited per day by S. tetras<br />
tetras grown at 28°C in culture ranged from 2.6 ng for individuals<br />
100-120 µm diagonal dimension to 10 ng for those 221 to 240 µm<br />
in size. Growth curves in culture were highly variable with some<br />
individuals growing continuously while others grew sporadically. The<br />
abundances of S. tetras tetras during March to August are reported.<br />
Peak abundances occurred in June and July during the warmer part of<br />
the seasonal temperature cycle. The mean skeletal weight of S.<br />
tetras tetras in plankton tows based on six representative samples<br />
was 41.8 µg/m 3 .<br />
Arcilla, C.A., Ruelo, H.B. & Umbal, J. 1989. The<br />
Angat Ophiolite, Luzon, Philippines; lithology, structure,<br />
and problems in age interpretation. In: Ophiolites and crustal<br />
genesis in the Philippines. (Flower, M.F.J., Eds.), vol.<br />
168/1-3. Tectonophysics, pp. 127-135.<br />
The Angat ophiolite is an incompletely unroofed and structurally<br />
dissected ophiolitic mass consisting of layered and massive<br />
gabbros, diabase sheeted dikes, tonalites, and pillow basalts.<br />
Mapping in the Montalban quadrangle has revealed complex<br />
structural relationships between pillow basalts and overlying<br />
sediments which hinder an accurate determination of ophiolite age.<br />
Sparse <strong>radiolaria</strong>n data suggest a Cretaceous age, but<br />
undifferentiated as to Early or Late Cretaceous. The structural<br />
deformation of the ophiolite is probably due in part to strike-slip<br />
faulting during Early to Middle Miocene time, this date being<br />
constrained by deformed sediments in fault contact with the<br />
ophiolite. Initial geochemical data from sheeted dikes and pillow<br />
lavas clearly related to the ophiolite show unusually high silica<br />
contents, and trace-element discrimination suggests that different<br />
- 24 -<br />
magma types may have been associated with the ophiolite. Pillow<br />
basalts that are probably genetically unrelated to ophiolite were also<br />
mapped close to the Angat ophiolite. Ages and tectonic settings<br />
determined from sedimentary rocks overlying these basalts should<br />
not be used to constrain age and paleotectonic interpretations of the<br />
ophiolite.<br />
Baldauf, J.G., Clement, B., Aksu, A.E., De<br />
Vernal, A., Firth, J., Hall, F., Head, M.J.,<br />
Jarrad, R., Kaminski, M.A., Lazarus, D.,<br />
Monjanel, A.L., Berggren, W.A., Gradstein, F.,<br />
Knuttel, S., Mudie, P. & Russel, M.D.J. 1989.<br />
Magnetostratigraphic and biostratigraphic synthesis of<br />
Ocean Drilling Program Leg 105: Labrador Sea and Baffin<br />
Bay. In: Proceedings of the Ocean Drilling Program,<br />
Scientific Results. (Srivastava, S.P., Arthur, M.A., Clement,<br />
B. et al., Eds.), vol. 105. College Station, TX (Ocean<br />
Drilling Program), pp. 935-956.<br />
During Ocean Drilling Program (ODP) Leg 105, three sites<br />
(Sites 645 through 647) were drilled in Baffin Bay and the Labrador<br />
Sea to examine the tectonic evolution and the climatic and oceanic<br />
histories of this region. Biostratigraphic and magnetostratigraphic<br />
results vary at each site, while stratigraphic resolution depends on<br />
the limited abundance of marker species and the completeness of<br />
the paleomagnetic record. Because of the paucity of planktonic<br />
microfossils and the poor paleomagnetic record signatures,<br />
stratigraphic determinations at Site 645 often rely on defining<br />
minimum temporal constraints on specific samples or stratigraphic<br />
intervals. The completed stratigraphy indicates that the sedimentary<br />
sequence recovered at Site 645 is early Miocene to Holocene in age.<br />
The magnetostratigraphy and biostratigraphies are better<br />
defined at Sites 646 and 647 in the Labrador Sea. Site 646<br />
generally contains a well-developed magnetostratigraphy and<br />
calcareous microfossil biostratigraphy. This biostratigraphy is based<br />
on calcareous nannofossils and planktonic foraminifers typical of<br />
the North Atlantic Ocean. Siliceous microfossils are also present at<br />
Site 646, but they are restricted to upper Pliocene through Holocene<br />
sediments. The stratigraphic sequence recovered at Site 646 is late<br />
Miocene to Holocene in age. Based primarily on the calcareous<br />
nannofossil stratigraphy, the sequence recovered at Site 647<br />
consists of lower Eocene to lower Oligocene, lower Miocene, upper<br />
Miocene, and upper Pliocene through Holocene sediments. Three<br />
hiatuses are present in this sequence. the older hiatus separates<br />
lower Oligocene sediments from lower Miocene sediments, another<br />
hiatus separates lower Miocene sediments from upper Miocene<br />
sediments, and the youngest one separates upper Miocene from<br />
upper Pliocene sediments. A magnetostratigraphy is defined for the<br />
interval from the Gauss/Matuyama boundary through the Brunhes<br />
(Clement et al., this volume). Both planktonic foraminifers and<br />
siliceous microfossils have restricted occurrences. Planktonic<br />
foraminifers occur in Pliocene and younger sediments, and siliceous<br />
microfossils are present in lower Miocene and lower Oligocene<br />
sediments.<br />
The near-continuous Eocene through lower Oligocene sequence<br />
recovered at Site 647 allows the calcareous nannofossils and<br />
diatom stratigraphies at this site to act as a Paleogene stratigraphic<br />
framework. This framework can be compared with the stratigraphy<br />
previously completed for DSDP Site 112.<br />
Ballance, P.F., Barron, J.A., Blome, C.D.,<br />
Bukry, D., Cawood, P.A., Chaproniere, G.C.H.,<br />
Frisch, R., Herzer, R.H., Nelson, C.S.,<br />
Quinterno, P., Ryan, H., Scholl, D.W.,<br />
Stevenson, A.J., Tappin, D.G. & Vallier, T.L.<br />
1989. Late Cretaceous pelagic sediments, volcanic ash and<br />
biotas from near the Louisville hotspot, Pacific plate,<br />
paleolatitude ~42 S. Palaeogeogr. Palaeoclimatol.<br />
Palaeoecol., 71/3-4, 281-299.<br />
Dredging on the deep inner slope of the Tonga Trench,<br />
immediately north of the intersection between the Louisville Ridge<br />
hotspot chain and the trench, recovered some Late Cretaceous<br />
(Maestrichtian) slightly tuffaceous pelagic sediments. They are<br />
inferred to have been scraped off a recently subducted Late<br />
Cretaceous guyot of the Louisville chain. In the vicinity of the<br />
Louisville hotspot (present location 50°26'S, 139°09'W; Late<br />
Cretaceous location ~42°S, longitude unknown) Late Cretaceous rich<br />
diatom, <strong>radiolaria</strong>n, silicoflagellate, foraminiferal and coccolith<br />
biotas, accumulated on the flanks of the guyot and are described in<br />
this paper. Rich sponge faunas are not described. ?Inoceramus<br />
prisms are present. Volcanic ash is of within-plate alkalic character.<br />
Isotope ratios in bulk carbonate ∂ 18 O -2.63 to +0.85, ∂ 13 C +2.98<br />
to 3.83) are normal for Pacific Maestrichtian sediments. The local<br />
CCD may have been shallower than the regional CCD, because of<br />
high organic productivity. In some samples Late Cretaceous<br />
materials have been mixed with Neogene materials. Mixing may have
Radiolaria 14 Bibliography - 1989<br />
taken place on the flanks of the guyot during transit across the<br />
western Pacific, or on the trench slope during or after subduction<br />
and offscraping about 0.5 Ma.<br />
Bechennec, F., Le Métour, J., Rabu, D., Beurrier,<br />
M., Bourdillon-Jeudy de Grissac, C., De Wever,<br />
P., Tegyey, M. & Villey, M. 1989. Géologie d'une<br />
chaîne issue de la Téthys: Les montagnes d'Oman. Bull. Soc.<br />
géol. France, 5/2, 167-188.<br />
The Oman mountains are a composite orogenic belt that was<br />
built during two major orogenic cycles: the Eo-Alpine cycle, that<br />
terminated with the overthrusting of the Hawasina nappes and the<br />
obduction of a part of the Tethyan oceanic crust onto the Arabian<br />
platform, and the Alpine cycle, during which the present mountain<br />
range was uplifted. The basement to the Oman mountains itself<br />
consists of two parts, one part that was deformed and<br />
metamorphosed during an old Panafrican cycle, and a sedimentary<br />
and volcanic part (autochthonous unit A) that was weakly deformed<br />
during a younger Panafrican and the Hercynian cycle. The Eo-Alpine<br />
cycle began in the late Permian with the transgression of the<br />
fusulinid sea onto the northern edge of Gondwana, and crustal<br />
extension within Gondwana that gave rise to the Hamrat Duru basin.<br />
Renewed extension during the Triassic led to the formation of the<br />
Umar basin, Misfah horst and Aridh trough on the internal side of the<br />
Hamrat Duru basin, these four structures together constituting the<br />
Hawasina basin. The Jurassic was a period of quiescence, preceding<br />
a further phase of extensional tectonism during the late Tithonian-<br />
Berriasian, which provoked the foundering of the northeastern edge<br />
of the Arabian platform, the westward retreat of the continental<br />
slope and subsidence of the Hawasina basin. Majolica facies<br />
sediments were deposited on the former platform, and the Hawasina<br />
basin, most of which was below the CCD, was characterized by the<br />
deposition of siliceous pelagic sediments. During the early<br />
Cretaceous the process was reversed, the submerged parts of the<br />
platform being covered by a regressive mega-sequence and in the<br />
Hawasina basin carbonate turbidites reappared. During the late<br />
Albian-early Cenomanian times, the oceanic Samail basin opened on<br />
the southern margin of the newly-formed Tethys. In the late<br />
Cretaceous the Eo-Alpine Oman mountain belt was built on the<br />
northeast edge of the Arabian platform. The Eo-Alpine orogeny was<br />
characterized by two main events. One was the subduction of the<br />
northeastern promontory of the Arabian platform, commencing<br />
during the Turonian, which was accompanied by the development of<br />
oceanward-verging tangential shears, and, on the internal edge of<br />
the platform (the Saih Hatat area), by HP-LT metamorphism The<br />
other main event was the closure of the Samail oceanic basin, that<br />
started during the late Turonian-Coniacian times, and resulted in the<br />
thrusting of the Samail ophiolite nappe together with the<br />
sedimentary Hawasina nappes onto the foreland. Obduction was<br />
followed by uplift of the Eo-Alpine mountains whose erosion began<br />
during the Maastrichtian. The Eo-Alpine phase was succeeded by an<br />
Alpine cycle between Maastrichtian and Burdigalian times<br />
characterized by unstable platform sedimentation and giving the<br />
Oman mountains their present-day architecture.<br />
Blome, C.D., Reed, K.M. & Tailleur, I.L. 1989.<br />
Radiolarian biostratigraphy of the Otuk Formation in and<br />
near the National Petroleum Reserve in Alaska. In: Geology<br />
and exploration of the National Petroleum Reserve in Alaska,<br />
1974 to 1982. (Gryc, G., Ed.), vol. 1399. United States<br />
geological Survey, professional Paper, Report, pp. 725-776.<br />
Bedded chert is a common rock type in the Brooks Range orogen<br />
of northern Alaska and is locally abundant in all parts of the orogen<br />
except the northeast brooks Range. Pennsylvanian to Jurassic<br />
<strong>radiolaria</strong>n chert is especially widespread in the west, in and<br />
adjacent to the De Long Mountains. The Cretaceous Brookian<br />
orogeny superposed and disordered the bedded chert sequences.<br />
Initial fore shortening and subsequent Laramide-style deformation<br />
created a complex of Carboniferous to Jurassic sedimentary<br />
deposits that has been rearranged into a stack of thrust sheets,<br />
each distinguished by its own physical, paleontologic, and tectonic<br />
characteristics (Mayfield and others, chapter 7, 1983b).<br />
Biostratigraphic control in our study was inadequate to refine many<br />
of the earlier paleontologic syntheses (Tailleur and others, 1966;<br />
Brosgé and Tailleur, 1970). Verification of the ages for <strong>radiolaria</strong>n<br />
cherts was particularly difficult because the only age diagnostic<br />
megafossils were found in the younger horizons. The older parts of<br />
the Otuk Formation (Mull and others, 1982) have yielded few useful<br />
megafossils.<br />
Renewed investigations of the National Petroleum Reserve in<br />
Alaska (NPRA) in the middle and late 1970's corresponded closely<br />
with development of a land-based Mesozoic <strong>radiolaria</strong>n zonal scheme<br />
pioneered by Pessagno (1976, 1977a, b). Nearly a thousand chert<br />
samples from various field projects and from one well were<br />
processed for <strong>radiolaria</strong>ns during an 8-yr period in the hope that the<br />
<strong>radiolaria</strong>n biostratigraphy might refine the ages of the various chert<br />
sequences. Investigations of resources other than hydrocarbons in<br />
- 25 -<br />
1977 and 1978 by Michael Churkin, Jr., Inyo Ellersieck, Carl Huie,<br />
D.L. Jones, C.F. Mayfield, W.J. Nokleberg, I.L. Tailleur, D.L. Vickery,<br />
and G.R. Winkler produced a set of mostly uncontrolled samples from<br />
the southern part of the NPRA and the foothills belt eastward to<br />
Tiglukpuk Creek (fig. 33.1A). During large-scale mapping in 1978,<br />
1979, and 1981 by D.C. Blanchard, S.M. Curtis, Ellersieck, Mayfield,<br />
and Tailleur, a large set of chert samples was collected from the De<br />
Long Mountains, Misheguk Mountain, and Noatak 1:250,000 scale<br />
quadrangles in the western Brooks Range. In 1978, R.J. Witmer and<br />
Tailleur collected samples from sections near the Lisburne well in<br />
the southern part of the NPRA. W.W. Chamberlain, B.L. Murchey, P.B.<br />
Swain, and Witmer systematically sampled several locations in the<br />
same area during the 1979 field season (Murchey and others,<br />
1981). During the 1980 field season, Murchey and Tailleur<br />
collected samples from reference sections in the lowest allochthon,<br />
on the Kiruktagiak River (lat 68°44'15'' N., long 152°20'00'' W.); on<br />
Tiglukpulc Creek, 150 km east of the NPRA; and from Agate Rock on<br />
the Lisburne Peninsula, 175 km west of the NPRA. J.S. Kelley<br />
sampled several sections in the lowest thrust sheet between the<br />
NPRA and Tiglukpuk Creek in 1982. Some of Tailleur's 1982<br />
samples were collected at sections near Mount Annette (100 km<br />
east of Chandler Lake quadrangle). K.M. Reed and Tailleur collected<br />
<strong>radiolaria</strong>n chert on the Lisburne Peninsula in 1982. Projects headed<br />
by C.G. Mull (Alaska Division of Geological and Geophysical Surveys)<br />
and Kelley continued to supply Brooks Range cherts for age analysis<br />
(see also Bodnar, 1984). The success of <strong>radiolaria</strong>n biostratigraphy,<br />
together with endothyroid and molluscan dating, has greatly aided<br />
recent geological mapping (Mayfield and others, chapter 8; Curtis<br />
and others, 1982, 1983, 1984; Ellersieck and others, 1982, 1983,<br />
1984; Mayfield and others, 1982, 1983a, b, 1984a, b, 19~7).<br />
This study includes <strong>radiolaria</strong>n faunas from lithostratigraphic<br />
sections through the Otuk Formation (fig. 33.2) that include shale,<br />
chert, and limestone of Triassic through Early Jurassic age. Our<br />
biostratigraphic scheme for the Otuk Formation is based on<br />
<strong>radiolaria</strong>n and molluscan faunal assemblages from measured<br />
sections, as well as correlation with <strong>radiolaria</strong>n faunas described in<br />
recent reports (through 1987) concerning Triassic faunas from Baja<br />
California, Oregon, British Columbia and Japan.<br />
Blueford, J.R. 1989. Radiolarian evidence: Late<br />
Cretaceous through Eocene ocean circulation patterns. In:<br />
Siliceous Deposits of the Tethys and Pacific Regions. (Hein,<br />
J.R. & Obradovic, J., Eds.). Springer-Verlag, New York. pp.<br />
19-29.<br />
Radiolarian assemblages, in Late Cretaceous through Eocene<br />
biosiliceous sediments, can help trace major paleocirculation<br />
patterns. Abundant <strong>radiolaria</strong>ns today indicate normal saline,<br />
oceanic conditions, so their presence in the fossil record documents<br />
seaways analogous to areas of presentday <strong>radiolaria</strong>n deposition.<br />
The circulation patterns indicated by <strong>radiolaria</strong>n distributions<br />
support and slightly modify previous paleoceanographic models.<br />
During the Late Cretaceous, circulation in the equatorial belt was<br />
continuous from the Pacific through the regions of the present-day<br />
Atlantic and into the Caspian Sea-Ural Mountains of the Soviet<br />
Union. Seaways connecting the Arctic and North Pacific Ocean<br />
enabled a wide distribution of <strong>radiolaria</strong>n fauna. Paleocene<br />
<strong>radiolaria</strong>n deposits are not abundant, and may indicate a circulation<br />
pattern that became restricted. Oceanographic conditions that<br />
prevent siliceous deposition are many, including regressions,<br />
weakened upwelling, lack of dissolved silica, temperature, and other<br />
biological or physical conditions. The distribution of Eocene<br />
<strong>radiolaria</strong>ns indicates renewed wide circulation in the Paleogene<br />
oceans. Radiolarian distribution needs to be considered with other<br />
fossil assemblages and with paleomagnetic data to accurately<br />
reconstruct the positions of the continents and the oceanic<br />
circulation patterns.<br />
Bohrman, G. & Stein, R. 1989. Biogenic silica at ODP<br />
Site 647 in the Southern Labrador Sea: occurrence,<br />
diagenesis, and paleoceanographic implications. In:<br />
Proceedings of the Ocean Drilling Program, Scientific<br />
Results. (Srivastava, S.P., Arthur, M.A., Clement, B. et al.,<br />
Eds.), vol. 105. College Station, TX (Ocean Drilling<br />
Program), pp. 155-170.<br />
Eocene to Holocene sediments from Ocean Drilling Program<br />
(ODP) Site 647 (Leg 105) in the southern Labrador Sea,<br />
approximately 200 km south of the Gloria Drift deposits, were<br />
investigated for their biogenic silica composition. Three sections of<br />
different diagenetic alteration products of primary siliceous<br />
components could be distinguished: (I) opal-A was recorded in the<br />
Miocene and the early Oligocene time intervals with strongly<br />
corroded siliceous skeletons in the Miocene and mostly well<br />
preserved biogenic opal in the early Oligocene; (2) opal-CT<br />
precipitation occurs between 250-440 meters below seafloor<br />
(mbsf) (earliest Oligocene to late Eocene); (3) between 620-650<br />
mbsf (early/middle Eocene), biogenic opal was transformed to clay<br />
minerals by authigenesis of smectites. Using accumulation rates of
Bibliography - 1989 Radiolaria 14<br />
biogenic opal, paleoproductivity was estimated for the early<br />
Oligocene to late Eocene interval. A maximum productivity of<br />
biogenic silica probably occurred between 35.5 and 34.5 Ma (early<br />
Oligocene). No evidence for opal sedimentation during most of<br />
middle Eocene was found. However, at the early/middle Eocene<br />
boundary (around 52 Ma), increased opal fluxes were documented by<br />
diagenetic alteration products of siliceous skeletons.<br />
Bohrmann, G. & Thiede, J. 1989. Diagenesis in<br />
Eocene claystones, ODP site 647, Labrador Sea: formation of<br />
complex authigenic carbonates, smectites, and apatite. In:<br />
Proceedings of the Ocean Drilling Program, Scientific<br />
Results. (Srivastava, S.P., Arthur, M., Clement, B. et al.,<br />
Eds.), vol. 105. College Station, TX (Ocean Drilling<br />
Program), pp. 137-154.<br />
Authigenic carbonates were recovered in lower to middle<br />
Eocene claystones at Ocean Drilling Program Site 647 in the<br />
Labrador Sea. Detailed chemical, petrographic, and X-ray<br />
investigations reveal that these diagenetic carbonates have a<br />
complex mineralogical composition. At least five different carbonate<br />
phases are identified: calcium-rich rhodochrosite, rhodochrosite,<br />
manganosiderite, siderite, and calcite. Manganese carbonates are<br />
the dominant carbonate phases formed throughout the section.<br />
Textural analyses show two major generations of carbonate<br />
formation. Early cementation of micritic carbonate in burrow<br />
structures was followed by carbonate cementation forming<br />
microsparry to sparry crystals.<br />
At approximately 620 meters below seafloor (mbsf), three<br />
concretions of iron carbonates occur, which indicates a special porewater<br />
chemistry. Thin section analyses from this level show (I)<br />
several generations of diagenetic carbonates, (2) widespread<br />
secondary cavity formation in burrow structures, and (3) various<br />
cement precipitations in voids. We suggest that this level<br />
represents a hiatus or highly condensed sequence, as indicated by<br />
(I) the low carbonate content in host sediments, (2) carbonate<br />
dissolution reflected by the high ratio of benthic to planktonic<br />
foraminifers, and (3) complex diagenetic alteration in the carbonate<br />
concretions.<br />
Iron and manganese enrichments observed in lithologic Unit IV<br />
may have been derived from a hydrothermal source at the adjacent,<br />
then active, Labrador Sea mid-ocean ridge. Authigenic smectites<br />
forming numerous pseudomorphs of siliceous microfossils are<br />
precipitated in burrow structures. We propose that diagenetic<br />
smectite formation from biogenic opal and iron oxyhydroxide<br />
(analogous to smectite formation in surface sediments of the East<br />
Pacific area) occurred in the Labrador Sea during the early and<br />
middle Eocene.<br />
Boltovskoy, D. 1989a. Radiolarian record of the last<br />
40,000 years in the western equatorial Pacific. Oceanologica<br />
Acta, 12/1, 79-86.<br />
Polycystine <strong>radiolaria</strong>ns were studied in two box cores (ERDC<br />
123 Bx and ERDC 129 Bx) from the Western equatorial Pacific<br />
Ocean (approx. 1°S, 161°E), sampled At 3 cm intervals from top (ca.<br />
0 to 4000-6000 YBP) to bottom (approx. 16000 and 40000 YBP,<br />
respectively). A total of 141 taxa were identified. Radiolarian<br />
assemblages were qualitatively and quantitatively (relative<br />
abundances) very similar, both between cores and between samples;<br />
Octopyle stenozona/Tetrapyle octacantha was by far the most<br />
abundant form at all levels, followed in decreasing proportions by<br />
Tholospyris spp., Stylodictya multispina, Botryocyrtis scutum, and<br />
Didymocyrtis tetrathalamus No significant changes in the specific<br />
composition of relative proportions of the taxa were found in<br />
association with the 18,000 YBP level. Slight evidence of an<br />
environmental change ca. 25,000 YBP was suggested by peaks of<br />
two <strong>radiolaria</strong>ns which presently characterize the more fertile<br />
Eastern equatorial Pacific waters (O. stenozona/T. octacantha and<br />
Euchitonia/Dictyocoryne spp.), and by an increase in the relative<br />
contribution of two colder- and deeper-water species below this<br />
level.<br />
Boltovskoy, D. 1989b. Las zonas de transición en la<br />
pelagial: biogeografía y paleobiogeografía. In: Memorias do<br />
III encontro Brasileiro de Plancton, Caioba, (PR). (Brandini,<br />
F.P., Eds.). Curitiba, Brasil. pp. 10-24.<br />
Boltovskoy, D., Alder, V.A. & Spinelli, F. 1989.<br />
Summer Weddell Sea microplankton: assemblage structure,<br />
distribution and abundance, with special emphasis on the<br />
Tintinnina. Polar Biol., 9, 477-456.<br />
Boltovskoy, D. & Vrba, A. 1989. Latitude-related<br />
shell patterns in Radiolaria; Botryostrobus auritus/australis<br />
- 26 -<br />
morphotypes in the equatorial to Antarctic Pacific. Mar.<br />
Micropaleontol., 13/4, 309-323.<br />
Analyses of the size, porosity and shape of 366 specimens of<br />
Botryostrobus auritus/australis retrieved from 17 surface sediment<br />
samples distributed more or less evenly between the equator and<br />
64° S in the western Pacific Ocean show that most shape-related<br />
features vary rather evenly from the tropics to the pole, suggesting<br />
a close relationship with surface temperature and/or salinity; the<br />
size and porosity of the shells, on the other hand, are more closely<br />
associated with primary productivity in the upper layers than with<br />
latitude. Most changes are smooth and stepwise, although for<br />
several characters there is an increase in the average rate of<br />
variation in the southernmost tropical to northern subantarctic<br />
areas, in coincidence with the zone of the species' maximum relative<br />
abundance. It is concluded that the morphologic differences studied<br />
are not consistent enough as to justify the division of B.<br />
auritus/australis into several distributionally more restricted taxa.<br />
On the other hand, the overlap for the ranges of most traits in the<br />
various climatic zones transected is of such magnitude that it<br />
restricts the potential usefulness of the shape, porosity and size<br />
patterns surveyed as ecologic or paleoecologic indicators.<br />
Braun, A. 1989a. Neue unterkarbonische Radiolarien-Taxa<br />
aus Kieselschiefer-Gerollen des unteren maintales be<br />
Frankfurt a. M. Geologica et Paleontologica, 23, 83-99.<br />
From pebbles of Lower Carboniferous siliceous shales (age:<br />
Upper Tournaisian, Tn 3c; = Middle Osagean) from the lower Mainvalley<br />
near Frankfurt a. M. (Germany) the following <strong>radiolaria</strong>nspecies<br />
and -subspecies are described: Albaillella indensis ambigua<br />
n. ssp., Ceratoikiscum umbraculum bisulcatum n. ssp., Archocyrtium<br />
callimorphum n. sp., Archocyrtium eupectum n. sp., Archocyrtium<br />
ferreum n. sp., Entactinia tortispina, Entactinia vulgaris microporata<br />
n. ssp., Entactinia? brilonensis, Entactinia? pantotolma n. sp.,<br />
Entactinosphaera? trendalli, Triaenosphaera minuscula n. sp.,<br />
Pylentonema eucosmeta n. sp. and Polyentactinia sp., aff. P. aranea.<br />
A complete list now includes 27 taxa of the species group in the<br />
rocks described. The total number of taxa at the species level<br />
present in one sample originally has been about 50-60. The<br />
multiplicity of forms in Lower Carboniferous <strong>radiolaria</strong>n faunas has<br />
presumably been lower than in Cenozoic and recent faunas.<br />
Braun, A. 1989b. Eine Radiolarian-Fauna aus dem Ober-<br />
Viseum des Dinant-Beckens (Belgien). Geologica et<br />
Paleontologica, 23, 101-111.<br />
9 <strong>radiolaria</strong>n species from 8 genera are described in open<br />
nomenclature from Upper Visean (Upper V3c, age determination<br />
based on Foraminifera) phosphorite-nodules of the Dinant-Basin<br />
(Belgium). The pyritized fauna contains representatives of the<br />
Albaillellidae, Ceratoikiscidae and Entactiniidae as well as two<br />
genera (Polyentactinia, Provisocyntra?) of uncertain family<br />
assignation. Latentifistulidae, Pylentonemidae and Archocyrtiidae<br />
have not been found. The Entactiniidae are represented<br />
predominantly by forms with long, threebladed spines. In the<br />
Albaillellidae only strongly segmented specimens are found.<br />
Provisocyntra? is probably present in a transitional form between<br />
Provisocyntra and the Upper Carboniferous-Permian genus<br />
Copycyntra, which, although theoretically postulated, has not been<br />
found up to now.<br />
Braun, A. 1989c. Unterkarbonische Radiolarien aus<br />
Kieselschiefergerollen des Mains bei Frankfurt am Main.<br />
Jber. Mitt. oberrh. geol. Ver., N.F., 71, 357-380.<br />
13 common Radiolarian species from lower Carboniferous<br />
siliceous shales occurring as pebbles in Pleistocene gravel deposits<br />
of the Main river near Frankfurt (West Germany) are figured and<br />
described. Source area for these pebbles is the Frankenwald. The<br />
abundance and fossil content of the pebbles give important hints<br />
concerning the age and local dissemination of lower Carboniferous<br />
siliceous deposits in the Frankenwald.<br />
Carter, E.S., Orchard, M.J. & Tozer, E.T. 1989.<br />
Integrated ammonoid-conodont-<strong>radiolaria</strong>n biostratigraphy<br />
Late Triassic Kunga Group, Queen Charlotte Islands, British<br />
Columbia. Geol. Surv. Canada, curr. res., Pap., 89-1H, 23-<br />
30.<br />
Ammonoids, conodonts, and <strong>radiolaria</strong>ns occur together in the<br />
Upper Carnian and Norian parts of the Kunga Group on Queen<br />
Charlotte Islands. The faunas provide a unique opportunity to<br />
establish a three-way integrated zonation for much of the Late<br />
Triassic. This complements what has previously been accomplished<br />
in northeast Pritish Columbia using the ammonoid standard and<br />
associated conodonts of the Pardonnet Formation. The latter<br />
zonation, established in a mid-paleolatitude area, is applicable to the<br />
Kunga Group (Wrangell) sequences for the most part, but low
Radiolaria 14 Bibliography - 1989<br />
paleolatitude aspects of some faunas is suggested. New conodont<br />
zonation for the Upper Carnian, and new <strong>radiolaria</strong>n zonation for<br />
much of the studied interval is expected. New and existing fossil<br />
zonation will provide a fundamental key in sedimentological,<br />
stratigraphic and structural studies of the Upper Triassic both on<br />
the Queen Charlotte Islands and elsewhere.<br />
Casey, R.E. 1989. Model of modern polycystine<br />
<strong>radiolaria</strong>n shallow-water zoogeography. In: Biological<br />
paleoceanography; plankton, productivity and carbon in<br />
ancient marine systems. A selection of papers presented at<br />
the fourth North American paleontological convention.<br />
(Eicher, D.L. et al., Eds.), vol. 74/1-2. Palaeogeography,<br />
Palaeoclimatology, Palaeoecology, pp. 15-22.<br />
There appear to be about six shallow-water polycystine<br />
<strong>radiolaria</strong>n provinces in the modern ocean. These provinces owe their<br />
integrity to the major circulation systems that create packages of<br />
water and environments which vary in degrees of oceanographic and<br />
temporal stability. The subpolar cyclonic gyres are low-diversity<br />
provinces dominated by the <strong>radiolaria</strong>n groups, cenodiscids,<br />
spongodiscids, spongotrochins, lithelids, and lophophaenins (some of<br />
these members exhibit the phenomenon of tropical submergence).<br />
Endemism is moderate in the southern subpolar cyclonic gyre. This<br />
gyre contains such endemic forms as antarctisins. The transition<br />
province contains a moderate-diversity fauna dominated by coldwater<br />
morphotypes of warm-water sphere taxa and a few endemics;<br />
however, this transition province appears to be a region of<br />
<strong>radiolaria</strong>n isolation and evolution. The subtropical anticyclonic gyre<br />
province exhibits the highest <strong>radiolaria</strong>n diversities, densities, and<br />
endemism of any of the provinces. This province is dominated by<br />
<strong>radiolaria</strong>ns that host symbiotic algae, and this association might<br />
possibly explain why they dominate these oiigotrophic regions. The<br />
equatorial province is very similar to the subtropical anticylonic gyre<br />
province; however, it does not exhibit as high a diversity, density, or<br />
degree of endemism as does the gyre. The eastern tropical province<br />
is dominated by symbiont-bearing <strong>radiolaria</strong>ns as is the subtropical<br />
anticyclonic gyre; however, unlike the gyre, there are few endemics<br />
and only low to moderate diversities and densities. The main reason<br />
for few endemics in the eastern tropical province is probably due to<br />
the youth of this province (it has only existed since the mid-<br />
Pliocene, whereas the subtropical anticyclonic gyre province has a<br />
history extending into the mid-Miocene). The boundary current<br />
"provinces" are really just tappings of the equatorial, subpolar, or<br />
transition provinces and reflect these parental provinces in their<br />
<strong>radiolaria</strong>n characteristics.<br />
Casey, R.E., Weinheimer, A.L. & Nelson, C.O.<br />
1989. California El Niños and related changes of the<br />
California current system from Recent and fossil <strong>radiolaria</strong>n<br />
records. In: Aspects of climate variability in the Pacific and<br />
the western Americas. (Peterson, D.H., Eds.), vol. 55.<br />
Geophysical Monograph, pp. 85-92.<br />
For the first time Lower Permian Radiolaria are described from<br />
Western Sicily, so far unknown from the whole Tethyan Eurasia. The<br />
fauna derives from olistoliths of dark gray, partly silty, hard<br />
marlstones and marly limestones without any macrofauna and from<br />
<strong>radiolaria</strong>n micrites. Radiolarians, clearly dominated by Albaillellacea<br />
DEFLANDRE, 1952 (Spinodefrandrella ? siciliensis n. sp.,<br />
Pseudoalbaillella scalprata scalprata HOLDSWORTH & JONES, 1980,<br />
P. scalprata postscalprata ISHIGA, 1983, P. scalprata<br />
praescalprata n. subsp., P. (Kitoconus) elongata ISHIGA & IMOTO,<br />
1980), are mostly the only fossils in these olistoliths. These<br />
<strong>radiolaria</strong>n faunas were until now known only from the Circumpacific<br />
area (P. scalprata scalprata also known from West Texas). They<br />
give the first evidence for the presence of pelagic Lower Permian in<br />
Sicily (topmost part of the Parafollicucullus lomentarius<br />
Assemblage-Zone of highest Artinskian or Lower Kungurian=Lower<br />
Jachtashian, P. ornatus Zone of Kungurian age and perhaps<br />
Pseudoalbaillella rhombothoracata A.-Z. of Late Kungurian to Early<br />
Chihsian age).<br />
Catalano, R., Di Stefano, P. & Kozur, H. 1989.<br />
Lower permian Albaillellacea (Radiolaria) from Sicily and<br />
their stratigraphic and paleogeographic significance. Rend.<br />
Accad. Sci. fis. mat., Ser. IV, 56, 1-24.<br />
For the first time Lower Permian Radiolaria are described from<br />
Western Sicily, so far unknown from the whole Tethyan Eurasia. The<br />
fauna derives from olistoliths of dark gray, partly silty, hard<br />
marlstones and marly limestones without any macrofauna and from<br />
<strong>radiolaria</strong>n micrites. Radiolarians, clearly dominated by Albaillellacea<br />
DEFLANDRE, 1952 (Spinodefrandrella ? siciliensis n. sp.,<br />
Pseudoalbaillella scalprata scalprata HOLDSWORTH & JONES, 1980,<br />
P. scalprata postscalprata ISHIGA, 1983, P. scalprata<br />
praescalprata n. subsp., P. (Kitoconus) elongata ISHIGA & IMOTO,<br />
1980), are mostly the only fossils in these olistoliths. These<br />
- 27 -<br />
<strong>radiolaria</strong>n faunas were until now known only from the Circumpacific<br />
area (P. scalprata scalprata also known from West Texas). They<br />
give the first evidence for the presence of pelagic Lower Permian in<br />
Sicily (topmost part of the Parafollicucullus lomentarius<br />
Assemblage-Zone of highest Artinskian or Lower Kungurian=Lower<br />
Jachtashian, P. ornatus Zone of Kungurian age and perhaps<br />
Pseudoalbaillella rhombothoracata A.-Z. of Late Kungurian to Early<br />
Chihsian age).<br />
From a paleogeographic point of view the findings of these<br />
faunas suggest that a broad pelagic belt connected the<br />
Circumpacific area and Sicily during the Lower Permian. This belt, as<br />
long as the Alpidic Orogen, was situated north of Gondwana and<br />
south of the later Tethyan median platforms.<br />
After the discovery of Middle Permian and Upper Permian<br />
(Abadehian, Dzhulfian) Albaillellaria, pelagic conodonts and<br />
psychrospheric Ostracoda, described in separate papers, can be<br />
assumed that the studied zone (Sicanian paleogeographic domain)<br />
was during the whole Permian an epioceanic area. Pelagic conditions<br />
lasted in this belt during the Mesozoic and Early Cenozoic. Apulia in<br />
the Permian was separated from Gondwanaland, but during its<br />
Mesozoic evolution was more near related to Africa.<br />
Chen, M.H. & Tan, Z.Y. 1989. Description of a new<br />
genus and 12 new species of Radiolaria in sediments from the<br />
South China Sea. Tropic Oceanol., 8/1, 1-9. (in Chinese)<br />
Cheng, Y.N. 1989. Upper Paleozoic and Lower Mesozoic<br />
<strong>radiolaria</strong>n assemblages from the Busuanga Islands, North<br />
Palawan Block, Philippines. Bull. natl. Mus. nat. Sci.,<br />
Taiwan, 1, 129-176.<br />
A preliminary field sampling from ribbon chert successions on<br />
Busuanga and Uson Islands yield abundant and well-preserved<br />
Radiolaria. Six <strong>radiolaria</strong>n assemblages can be recognized of which<br />
three assemblages are of Permian in age and three assemblages are<br />
of Triassic in age. They are tentatively named as: Albaillella cf.<br />
Ievis—Latentifustula cf. similicutis Assemblage, Follicucullus cf.<br />
scholasticus—Triplanospongos cf. musashiensis Assemblage,<br />
Neoalbaillella cf. optima Assemblage, Pesudoheliodiscus sp. F<br />
Assemblage, and Betraccium deweveri Assemblage. Twenty-nine<br />
species belonging to thirteen genera of the Upper Paleozoic<br />
albaillellids and stauraxon polycystins are illustrated. For Triassic<br />
(Ladinian to upper Norian) section, Radiolaria are much more<br />
diversified and totally sixty-four species belonging to twenty-three<br />
genera are illustrated.<br />
Cheng, Y.N. & Yeh, K.Y. 1989. Radiolaria in surface<br />
sediments from west central Pacific near Taiwan (I). Bull.<br />
natl. Mus. nat. Sci., Taiwan, 1, 177-212.<br />
This is the first in a series of reports dealing with recent<br />
<strong>radiolaria</strong>n studies for the west central Pacific near Taiwan. Based on<br />
the analyses of twenty six core tops, the results can be summerized<br />
as followings. (1) Radiolaria are rich in the fine-grain sediments from<br />
the basin to the southwest of Taiwan. (2) The major <strong>radiolaria</strong>n<br />
components of each sample are similar to one another at generic<br />
level. (3) All the <strong>radiolaria</strong>n assemblages are characterized by<br />
having distinct tropical forms and some subtropical taxa. (4) In the<br />
basin along the eastern coast of Taiwan, sediments containing<br />
Radiolaria were mostly collected from the southern part. According<br />
to the previous workers, this area could be an upwelling zone<br />
Coccioni, R., Franchi, R., Nesci, O., Wezel,<br />
F.C., Battistini, F. & Pallecchi, P. 1989.<br />
Stratigraphy and Mineralogy of the Selli Level (Early Aptian)<br />
at the Base of the Marne a Fucoidi in the Umbro-Marchean<br />
Apennines (Italy). In: Cretaceous of the Western Tethys.<br />
Proceedings 3rd International Cretaceous symposium,<br />
Tübingen 1987. (Wiedman, J., Eds.). E. Schweizerbart'sche<br />
Verlagsbuchhandlung, Stuttgart. pp. 563-584.<br />
Detailed, lithostratigraphical, biostratigraphical and<br />
mineralogical studies on the "ichthyolithic-bituminous-radiolaritic"<br />
regional marker-bed (named Selli Level), located just above the lower<br />
boundary of the Marne a Fucoidi Formation (early Aptian- late<br />
Albian) in the Umbro-Marchean Apennines, were carried out. This<br />
distinctive organic-rich level is 1- 3 m thick. It consists of<br />
mudstones alternating with <strong>radiolaria</strong>n silty and sandy layers.<br />
Radiolaria are the exclusive components of the microfaunal<br />
assemblage (belonging to the Stichocapsa euganea Zone) found in<br />
the level. The age of the level is Lower Aptian (Bedoulian).<br />
The main mineralogical composition of the Selli Level is<br />
characterized by the absence of calcite together with a high quartz<br />
content. Smectite, illite and illite-smectite mixed layers dominate<br />
the clay mineral fraction with some chlorite, chlorite-vermiculite and<br />
occasional kaolinite. Based on its mineralogical composition, the
Bibliography - 1989 Radiolaria 14<br />
level is distinctly different from the underlying and overlying<br />
sediments of the Marne a Fucoidi. The Selli Level is similar, in some<br />
respects, to the Bonarelli Level (dated close to the Cenomanian-<br />
Turonian boundary) which characterizes the uppermost part of the<br />
Scaglia Bianca in the Umbro-Marchean Apennines. Both the<br />
depositional sequences which include the above-mentioned markerbeds<br />
show a similar vertical trend. The Selli and Bonarelli Levels<br />
probably deposited under analogous palaeoceanographic conditions.<br />
Danelian, T. 1989. Radiolaires jurassiques de la zone<br />
Ionienne (Epire, Grèce) Paléontologie - Stratigraphie<br />
implications paléogéographiques. Ph.D. Thesis. Mém. Sci.<br />
Terre Univ. Curie, Paris, n. 89-25, 269 p.<br />
The Triassic-Lower Jurassic neritic platform is submitted to an<br />
extension regime during Liassic time (Ammonitico Rosso and<br />
associated rocks). A deep trough was established and siliceous<br />
deposits occurred. The continuity of this sedimentation was not<br />
established, no fauna were described from these beds. According to<br />
B.P.'s geologists (1971) the Upper Jurassic was missing, probably<br />
eroded, contrary to many authors (i.e. I.G.R.S.-I.F.P., 1966;<br />
BERNOULLI & RENZ, 1970) who supposed the sequence without<br />
hiatuses.<br />
Radiolarian fauna permit us to date the top of the "Calcaire a<br />
filaments" Formation (Bathonian and/or middle Callovian) and the<br />
Upper "Posidonia" Beds Formation: Bathonian and/or middle<br />
Callovian near the base, Upper Tithonian and/or Berriasian near the<br />
top. The base of the Vigla Limestone Formation is dated by Radiolaria<br />
and Calpionellids. These fauna establish an important diachronism,<br />
from lower Oxfordian to lower Berriasian. However, the Upper<br />
Jurassic age of the base of the Vigla Limestone is developed with a<br />
peculiar facies. The usual micritic Vigla Limestone contains<br />
Berriasian age fauna. These results document a continuity of<br />
sedimentation in the Ionian trough and permit us to withdraw (at<br />
least for Epirus) the hypothesis of an Upper Jurassic generalized<br />
stratigraphic gap. Nevertheless, many localized gaps exist. The time<br />
span of one stratigraphic gap (Middle Liassic to Upper Oxfordian),<br />
situated between the Pantokrator Limestone and the Upper<br />
"Posidonia" Beds has been well-documented in one of the studied<br />
sections and interpreted as a progressive transgression on tilted<br />
block.<br />
Radiolarian fauna from Jurassic formations of the Ionian zone<br />
(Epirus, Greece) yielded 110 identifiable species. They belong to 52<br />
genera. Eighty species were already known and formally described,<br />
30 others are presented in open nomenclature. Following the<br />
descriptions and citations by the different authors the age-range of<br />
73 species are synthetized. The previously admitted age-range of<br />
Tetraditryma praeplena is here modified.<br />
The Jurassic stratigraphic successions can be interpreted as<br />
extensional passive margins: (i) the pre-rift series correspond to the<br />
Pantokrator Limestone Formation (Upper Triassic-Lower Liassic); (ii)<br />
the syn-rift series begin with the Siniais and Louros Limestone<br />
Formations (Pliensbachian); (iii) the post-rift series start with the<br />
"Calcaires a filaments" Formation (Aalenian to Bathonian-middle<br />
Callovian). As suggested by DE WEVER et al. (1986), RICOU (1987),<br />
the sedimentation of the base of Vigla Limestone is tied to paleooceanographic<br />
changes in the Jurassic Tethys: the opening of the<br />
Atlantic ocean in the Caribbean domain generates a large oceanic<br />
seaway from E to W.<br />
Davis, H.R., Byers, C.W. & Pratt, L.M. 1989.<br />
Depositional mechanisms and organic matter in Mowry Shale<br />
(Cretaceous), Wyoming. Bull. amer. Assoc. Petroleum Geol.,<br />
73/9, 1103-1116.<br />
Four lithofacies, which accumulated under different<br />
depositional conditions, can be distinguished in the Lower<br />
Cretaceous Mowry Shale of Wyoming. Type and amount of organic<br />
matter in these lithofacies are governed largely by sediment<br />
transport mechanisms. Nearshore silt and mud containing terrestrial<br />
organic matter were deposited in a prodelta environment by tractive<br />
processes and from suspension. These sediments, along with<br />
terrestrial organic matter, were redistributed by waning bottom<br />
flows over a dysaerobic slope; pelagically deposited muds containing<br />
marine-derived organic matter accumulated between flow events.<br />
Muds farthest offshore accumulated in dysaerobic and anaerobic<br />
water by pelagic settling in a region unaffected by bottom currents;<br />
these muds contain predominantly marine-derived organic matter.<br />
Petroleum source potential increases in a southeast-ward<br />
direction across west and central Wyoming. This trend results from<br />
differential input of marine and terrestrial organic matter, clastic<br />
dilution, and postdepositional biodegradation.<br />
De Wever, P. 1989. Radiolarians, radiolarites, and<br />
Mesozoic paleogeography of the Circum-Mediterranean<br />
Alpine belts. In: Siliceous Deposits of the Tethys and Pacific<br />
- 28 -<br />
Regions. (Hein, J.R. & Obradovic, J., Eds.). Springer-Verlag,<br />
New York. pp. 31-49.<br />
Radiolarites are of great importance as bathymetric indicators<br />
for paleogeographic reconstructions and geodynamic models. Only<br />
recently have we been able to date radiolarites and many age dates<br />
are scattered through the specialized geologic literature. The<br />
inventory of available data from the Mesozoic of the circum-<br />
Mediterranean Alpine fold belts reveals two general periods of<br />
radiolarite sedimentation, both associated with sedimentary and<br />
ophiolitic sequences: one period occurred during Triassic and/or<br />
Liassic time, the other during Dogger and/or Malm time. The<br />
Triassic-Liassic sections are allochtonous. Radiolarites associated<br />
with extrusive rocks are considered to be the sedimentary cover of<br />
an oceanic crust, either of an open ocean, back-arc basin or small<br />
ocean basin. Radiolarites intercalated with other sedimentary rocks<br />
belong to nappes with unknown basement rocks, probably of thinned<br />
continental crust. Radiolarites deposited during Dogger and Malm<br />
time are of three types and characterize three environments whose<br />
common attribute is a basal diachronism and a synchronous top.<br />
Radiolarites intercalated with sedimentary sequences occurred in<br />
basins that received deposits since Triassic time (i.e., Lagonegro,<br />
Pindos-Olonos zone) or in regions newly invaded by water masses<br />
(i.e., Austro-Alpine zone). Detailed local studies suggest deposition<br />
on faulted blocks of a rifting margin. Although the base of<br />
radiolarites is not synchronous in different units, it nevertheless<br />
starts around the Dogger and the maximum development was<br />
generally during Oxfordian time. The base of radiolarites associated<br />
with ophiolites is everywhere dated as Malm but the bases are not<br />
exactly synchronous; data are still too few to analyze the details.<br />
The sudden disappearance of all the radiolarites in the Uppermost<br />
Jurassic may be attributed to a drastic change in circulation from<br />
gyres producing upwelling in the Tethyan basin, to latitudinal, eastto-west<br />
circulation through Central America which broke down the<br />
upwelling regime in much of the tethyan area.<br />
De Wever, P., Granlund, A. & Cordey, F. 1989.<br />
Icule. Un système d'analyse de contour d'image pour<br />
micropaléontologie, une étape vers un système<br />
paléontologique intègre. Rev. Micropaléont., 32/3, 215-<br />
225.<br />
The system ICULE — and Interactive Coordinate Utilisation on<br />
technique for Landmark Extraction — was developed for using image<br />
analysis in paleontology. With this technique it is possible to<br />
produce A quantitative paleontological base of informations suitable<br />
for comparable studies in various fields in geology and to define A<br />
model for an assemblage.<br />
Dosztály, L. 1989. Triassic <strong>radiolaria</strong>ns from Dallapuszta<br />
(Mount Darno, N. Hungary). M. All. Földtani Intézet évi<br />
jelentése, , 193-201.<br />
The age of the red radiolarite located at the flanks of Mount<br />
Darnó could be refined on the basis of the Radiolaria fauna. Within<br />
the sequence, a change in the fauna could be observed. There were<br />
separated from assemblage two subspecies of the species Sarla<br />
kretaensis KOZUR and KRAHL.<br />
Dumitrica, P. 1989. Internal skeletal structures of the<br />
superfamily Pyloniacea (Radiolaria), a basis of a new<br />
systematics. Rev. españ. Micropaleont., 21/2, 207-264.<br />
This paper is the first through study of the internal skeletal<br />
structures of the superfarnily Pyloniacea, a large group of Radiolaria<br />
entirely or partly built of systems of successively inverted or<br />
perpendicular girdles. Based on the investigation of hundreds of<br />
oriented sections through many Mesozoic and Cenozoic species the<br />
author analyses and describes the mode of skeleton growth, the<br />
structure of microsphere, systems of girdles, and spines. Having<br />
gates as any shell girdle the microsphere is regarded as the first<br />
girdle of the first system and one of the two fundamental taxonomic<br />
elements of the superfamily. The number of gates and their<br />
reciprocal position permit recognition of four main structural types<br />
of microspheres of high taxonomic value. Finally, a new systematics<br />
is proposed at family and subfamily levels. One family, 6<br />
subfamilies, 8 genera and 10 species are described as new, and the<br />
definitions of the other families and subfamilies are emended.<br />
Dyer, R. & Copestake, P. 1989. A review of Late<br />
Jurassic to earliest Cretaceous <strong>radiolaria</strong> and their<br />
biostratigraphic potential to petroleum exploration in the<br />
North Sea. In: Northwest European Micropaleontoogy and<br />
Palynology. (Batten, D.J. & Keen, M.C., Eds.). Ellis<br />
Horwood Limited for the British Micropalaeontological<br />
Society, Chichester, UK. pp. 213-235.<br />
The nature and biostratigraphic potential of Late Jurassic and<br />
earliest Cretaceous Radiolaria are reviewed in order to assess their
Radiolaria 14 Bibliography - 1989<br />
role for age dating, zonation and correlation of the Kimmeridge Clay<br />
Formation of the northern North Sea. 13 <strong>radiolaria</strong>n events are<br />
recognized, including species "tops", "acmes" and "bases" which<br />
are distributed throughout the Kimmeridge Clay Formation. The<br />
correlation of these events is discussed in two wells from the<br />
northern North Sea. This suggests that the group can provide an<br />
important contribution towards stratigraphic evaluation of the<br />
formation in offshore exploration wells. The taxonomy of certain<br />
stratigraphically important species is briefly reviewed.<br />
El Kadiri, K., Linares, A. & Olóriz, F. 1989. La<br />
Dorsale calcaire interne entre les Accidents de l'Oued Laou (Rif<br />
septentrional, Maroc): évolutions stratigraphique et<br />
géodynamique au cours du Jurassique-Crétacé. Comunic. Serv.<br />
geol. Port., 75, 39-65.<br />
Elorza, J.J. & Bustillo, M.A. 1989. Early and Late<br />
Diagenetic Chert in Carbonate Turbidites of the Senonian<br />
Flysch, northeast Bilbao, Spain. In: Siliceous Deposits of<br />
the Tethys and Pacific Regions. (Hein, J.R. & Obradovic, J.,<br />
Eds.). Springer-Verlag, New York. pp. 93-106.<br />
Sedimentological and petrographical analysis of the lower<br />
Senonian flysch (Plencia Fm.), near Barrika village, and a part of the<br />
upper Senonian flysch (Eibar Fm. ) show three types of diagenetic<br />
silicification: Bedded and nodular chert, chert in poorly developed<br />
laminites, and fracture-related chert. The beds and nodules of early<br />
formed chert and chert in laminites occur in the Tb, Tc, and Td Bouma<br />
intervals in the carbonate turbidites. The original sedimentary<br />
structures are preserved in the cherts. The fracture-related chert<br />
has a later diagenetic origin, and cross-cuts the sedimentary<br />
structures and the early-formed chert. Silica minerals include<br />
microquartz and length-fast chalcedony in the bedded, nodular, and<br />
fracture-related chert. Microquartz and length-slow chalcedony<br />
(quartzine) compose laminite-hosted chert.<br />
No differences exist in the abundance of minor elements among<br />
all the types of chert. The contents in Zr, Pb, Rb, and Zn are higher<br />
than the amounts commonly found in these types of cherts from<br />
other areas, and these elements may be associated with the iron<br />
oxides.<br />
The silica of the bedded and nodular chert was derived from the<br />
early dissolution and calcitization of sponge spicules and<br />
<strong>radiolaria</strong>ns mixed in with the carbonate turbidites. The late stage<br />
fracture-related chert apparently came from a later-stage<br />
calcitization of siliceous tests and perhaps also from a partial silica<br />
remobilization of the early-formed chert.<br />
Febvre, J. & Febvre-Chevalier, C. 1989a. Motility<br />
processes in Acantharia. II - A Ca 2+ dependent system of<br />
contractile 2-4 nm filamens isolated from demembranated<br />
myonemes. Biol. Cell, 67, 243-249.<br />
Myonemes of the acantharians are contractile ribbon-like<br />
organelles. As previously shown, their motility is based on the coiling<br />
mechanism of double-twisted 2—4 nm nonactin filaments.<br />
Myonemes have been isolated and manipulated in vitro. After<br />
demembranation, the contraction takes place when the Ca 2+<br />
concentration is above 10 -7 M, whereas relaxation occurs below this<br />
threshold concentration. The response to Ca 2+ ions is an on/off<br />
mechanism. Both contraction and relaxation can be induced<br />
repeatedly without fatigue phenomena- Other divalent cations such<br />
as Sr 2+ , Ba 2+ , Mn 2+ , CO 2+ , and La 3+ can replace Ca 2+ in inducing<br />
contraction of the demembranated myonemes although with less<br />
efficiency. Contraction and relaxation are ATP-independent and<br />
calmodulin ;s not involved in this in vitro motility process. The<br />
myoneme is a strongly resistant structure which is capable of<br />
contracting and relaxing under various extreme conditions which<br />
indicates very stable proteins and resistant functions.<br />
Febvre, J. & Febvre-Chevalier, C. 1989b. Motility<br />
and processes in Acantharia (Protozoa). III - Calcium<br />
regulation of the contraction-relaxation cycles of in vivo<br />
myonemes. Biol. Cell, 67, 251-261.<br />
The myonemes in the marine pelagic-protozoa Acantharia are<br />
contractile organelles involved in buoyancy regulation. It was<br />
previously shown that they can perform three kinds of movement:<br />
rapid contraction, slow undulation and slow relaxation. They consist<br />
of a periodically striated bundle of 2-4 nm nonactin fi!aments that<br />
are twisted in pairs and shortened by a coiling mechanism. After<br />
permeabilization or demembranation, contraction and relaxation can<br />
still be performed by varying Ca 2+ concentration and ATP is not<br />
needed.<br />
In the present paper, we have studied the role of Ca 2+ and<br />
inhibitors of energy production in intact cells. Our data suggest that;<br />
(i) the in vivo rapid contraction subsequent to mechanical or<br />
electrical stimulation is triggered by Ca 2+ influx across the cell<br />
- 29 -<br />
membrane; (ii) the slow contraction that takes place during the<br />
undulating movement depends on Ca 2+ release provided by internal<br />
calcium stores; (iii) the rapid contraction as well as the progressive<br />
shortening that occurs during the slow undulating movement are<br />
caused by Ca 2+ binding to the myoneme-filaments; (iv) ATP is not<br />
directly involved in the saturation by Ca 2+ of Ca 2+ sensitive sites<br />
located along the myoneme microstrands; (v) regulation of the<br />
movements of Ca 2+ within the cytoplasm depends mainly upon the<br />
alternative pathway of ATP production; (vi) calmodulin is presumably<br />
involved in this regulation. A tentative cytophysiologic interpretation<br />
of the mechanism of contractility is proposed.<br />
Fujita, H. 1989. Stratigraphy and geologic structure of the<br />
Pre-Neogene strata in the Central Ryukyu Islands. J. Sci.<br />
Hiroshima Univ., Ser. C: Geol. Min., 9/1, 237-284.<br />
The stratigraphy and geologic structure of the pre-Neogene<br />
strata in the northwestern Okinawa islands and the northern Amami<br />
islands were investigated in order to clarify the sedimentary and<br />
tectonic history of Central Ryukyu during the late Paleozoic to<br />
Paleogene period. The pre-Neogene strata of Central Ryukyu form an<br />
asymmetrically folded structure in each of the tectonic units<br />
separated by reverse or thrust faults dipping generally toward the<br />
northwest, and as a whole they form an imbricate structure. The pre-<br />
Neogene strata in the northwestern Okinawa islands are classified<br />
into the following formations roughly from northwest to southeast:<br />
Iheya, Izena, Maedake and Ie formations (Permian to early<br />
Cretaceous ?), Dana and Moromi formations (late Cretaceous ?),<br />
Nakijin formation (Carnian) and Gusukuyama formation (Oxfordian to<br />
Tithonian), Motobu formation (PermiantoTriassic?) and Yonamine<br />
formation (Valanginian to Barremian), Wakugawa formation (late<br />
Albian to Cenomanian ?), Nago formation (Cenomanian to Santonian<br />
?) and Kayo formation (early middle Eocene). The pre-Neogene<br />
strata in the northern Amami islands are divided, from west to east,<br />
into the Yuwan formation (Oxfordian to Berriasian), Yuwandake<br />
formation (Valanginian to middle Albian), Odana formation (late<br />
Albian to Cenomanian), Naze and Ogachi formations (Cenomanian to<br />
Santonian ?) and Wano formation (Eocene). Excepting the Dana,<br />
Moromi, Kayo and Wano formations, the pre-Neogene strata become<br />
generally younger from northwest or west to southeast or east in<br />
both districts. These pre-Neogene strata are characterized by the<br />
development of subaqueous slumping or sliding. Especially, the<br />
Yonamine, Yuwan and Yuwandake formations comprise a large<br />
amount of olistostromes in which olistoliths were derived chiefly<br />
from the northwestern area. The polarity in geological age toward the<br />
southeast and the inferred source of olistoliths may suggest that<br />
the sedimentary basins of thesepre-Neogene strata migrated southeastward<br />
during late Jurassic to late Cretaceous time.<br />
In the pre-Neogene strata, "slump structures" and tectonic<br />
structures are observed. The tectonic structures are classified into<br />
I, flexural slip folds; II, reverse faults and asymmetric folds with<br />
cleavages; III, thrust faults and associated folds; IV, strike slip<br />
faults; V, normal, lag and reverse faults. The tectonic structures I, II,<br />
and III take part in the asymmetrically folded and imbricated<br />
structure parallel to the extension of the pre-Neogene strata, while<br />
the tectonic structures IV and V cut it obliquely. The formation of<br />
the asymmetrically folded and imbricated structure in the pre-<br />
Neogene strata may be closely related to the migration of the<br />
sedimentary basins.<br />
Garrison, D.L. & Buck, K.R. 1989. Protozooplankton<br />
in the Weddell Sea, Antarctica: abundance and distribution in<br />
the ice-edge zone. Polar Biol., 9, 341-351.<br />
Protozooplankton were sampled in the ice-edge zone of the<br />
Weddell Sea during the austral spring of 1983 and the austral<br />
autumn of 1986. Protozooplankton biomass was dominated by<br />
flagellates and ciliates. Other protozoa and micrometazoa<br />
contributed a relatively small fraction to the heterotrophic biomass.<br />
During both cruises protozoan biomass, chlorophyll a<br />
concentrations, phytoplankton production and bacterial biomass and<br />
production were low at ice covered stations. During the spring<br />
cruise, protozooplankton, phytoplankton, and bacterioplankton<br />
reached high concentrations in a well-developed ice edge bloom<br />
~100 km north of the receding ice edge. During the autumn cruise,<br />
the highest concentrations of biomass were in open water wellseparated<br />
from the ice edge. Integrated protozoan biomass was<br />
20%.<br />
Bacterial biomass exceeded protozooplankton biomass at ice<br />
covered stations but in open water stations during the fall cruise,<br />
protozooplankton biomass reached twice that of bacteria in the<br />
upper 100m of the water column. The biomass of different<br />
protozoan groups was positively correlated with primary production,<br />
chlorophyll a concentrations and bacterial production and biomass,<br />
suggesting that the protozoan abundances were largely controlled by<br />
prey availability and productivity. Population grazing rates<br />
calculated from clearance rates in the literature indicated that<br />
protozooplankton were capable of consuming significant portions of<br />
the daily phyto- and bacterioplankton production.
Bibliography - 1989 Radiolaria 14<br />
Gawor-Biedowa, E. & Witwicka, E. 1989. Subclass<br />
Radiolaria Muller, 1858. In: Geology of Poland, Atlas of<br />
guide and characteristic fossils. (Malinowska, L., Eds.), vol.<br />
3/2c. Wydawnictwa Geol., Warsaw, Poland. pp. 1-218.<br />
Giese, M. & Schmidt-Effing, R. 1989. Eine<br />
Radiolarienfauna aus dem Unter-Karbon von Amonau bei<br />
Wetter (Rheinisches Schiefergebirge/Hessen). Geologica et<br />
Paleontologica, 23, 71-81.<br />
A well preserved <strong>radiolaria</strong>n fauna could be extracted from the<br />
phosphorite-nodules of the "Liegende Alaunschiefer" near Amonau<br />
(Wetter). This fauna is composed by 7 genera with 13 species. They<br />
belong to three stratigraphical groups. Group I consists of Albaillella<br />
cornuta, Archocyrtium climoceras, Archocyrtium coronaesimilae,<br />
Archocyrtium riedeli, Astroentactinia multispinosa, Ceratoikiscum<br />
apertum, Ceratoikiscum speciosum, Entactinia vulgaris and<br />
Popofskyellum undulatum and longs from the Lower Tournaisian to<br />
the Upper Visean. Group II consists of Albaillella paradoxa,<br />
Archocyrtium castuligerum and Ceratoikiscum avimexpectans and<br />
longs from the Lower to the Upper Tournaisian. Group III consists of<br />
Entactinia tortispina and longs from the Upper Tournaisian to the<br />
Upper Visean. Consequently the fauna has to be assigned to the<br />
Upper Tournaisian [Tn 3; to the Archocyrtium lagabrielli-Zone of<br />
GOURMELON (1987), although the index species has not been found<br />
up to now.].<br />
Goll, R.M. 1989. A synthesis of Norwegian Sea<br />
biostratigraphies: ODP Leg 104 on the Voring Plateau. In:<br />
Proceedings of the Ocean Drilling Program, Scientific<br />
Results. (Eldholm, O., Thiede, J., Taylor, E. et al., Eds.),<br />
vol. 104. College Station, TX (Ocean Drilling Program), pp.<br />
777-826.<br />
Summaries are presented of the 12 biostratigraphic<br />
contributions to this volume, which treat the calcareous, siliceous,<br />
and organic-walled microfossils preserved in the 1319.1 m of<br />
sediments and the thin shales intercalated in the 914.0-m-thick<br />
basalt series recovered on Leg 104. Biostratigraphic range data are<br />
synthesized into a lower Eocene to Pleistocene biostratigraphic<br />
framework for the sedimentary successions of the eight holes drilled<br />
at Sites 642, 643, and 644 on the Vøring Plateau. Upper Neogene<br />
successions 100.3 m thick at Site 643, 158.0-160.3 m thick at<br />
Site 642, and 252.8 m thick at Site 644 form a composite section<br />
that is regarded as 91% complete for the past 10.2 Ma. Aided by<br />
interpretable magnetic polarity records and discontinuous<br />
occurrences of calcareous microfossils, ages to the nearest 0.1 Ma<br />
are assigned to these sediments with reasonable confidence. Lower<br />
Neogene successions 117.7 m thick at Site 643 and 117.7 m thick<br />
at Site 642 form a composite section interpreted as 93% complete<br />
for the interval 13.4-23.5 Ma. Ages for these sediments are less<br />
confidently assigned as a result of the general absence of<br />
calcareous microfossils, more problematical polarity records and<br />
few tie points. Paleogene successions 155.2 m thick at Site 643<br />
and 1107.1 m thick (including the basalt series) at Site 642 pose<br />
difficult correlation problems, and ages assigned to these sediments<br />
are a compromise between dinoflagellate biostratigraphy and the<br />
benthic foraminifer biostratigraphy by Kaminski (1988). Microfossil<br />
distributions discussed in the synthesis include: actiniscidians,<br />
Bolboforma; calcareous nannofossils, diatoms, ebridians, benthic and<br />
planktonic foraminifers, ostracodes, palynomorphs, <strong>radiolaria</strong>ns, and<br />
silicoflagellates.<br />
Time intervals of 3.2 and 4.9 m.y. at Sites 642 and 643,<br />
respectively, are represented by a major late-middle to early-late<br />
Miocene hiatus. This and ten other hiatuses of lesser magnitude<br />
divide the Neogene sedimentary succession of the outer Vøring<br />
Plateau into ten sequences that are classified in a synthemic<br />
system. Leg 104 hiatuses are correlative with hiatuses recognized<br />
in the Pacific, and some appear to have equivalents in other regions<br />
of the Norwegian Margin and on the Jan Mayen Ridge. A<br />
biostratigraphic review of 14 Leg 38 sites indicates that the poorly<br />
understood Paleogene sedimentary successions of the Norwegian<br />
Sea may be represented by four major unconformity-bounded<br />
sequences of regional scope.<br />
Goll, R.M. & Bjørklund, K.R. 1989. A new<br />
<strong>radiolaria</strong>n biostratigraphy for the Neogene of the Norwegian<br />
Sea: ODP Leg 104. In: Proceedings of the Ocean Drilling<br />
Program, Scientific Results. (Eldholm, O., Thiede, J., Taylor,<br />
E. et al., Eds.), vol. 104. College Station, TX (Ocean<br />
Drilling Program), pp. 697-737.<br />
Radiolaria are present in frequencies ranging from rare to<br />
abundant and with generally moderate to good preservation quality in<br />
Leg 104 sediments younger than 22 Ma. Preservation degrades in<br />
progressively younger sediments, and upper Pliocene to mid-<br />
Pleistocene <strong>radiolaria</strong> were found only at Site 644, where sporadic<br />
assemblages of moderate to poorly preserved specimens persist to<br />
- 30 -<br />
approximately 0.75 Ma. Radiolaria are essentially absent in Leg 104<br />
recovery older than basal Miocene.<br />
The stratigraphic ranges of 55 taxa of Radiolaria are<br />
documented in 451 samples from the biosiliceous recoveries of<br />
Holes 642B, 642C, 642D, 643A, and 644A. The stratigraphic<br />
ranges of 25 of these species are used as boundary criteria for a<br />
new system of 28 Neogene zones and subzones that are used to<br />
characterize approximately 72% of the past 22 m.y. of<br />
sedimentation on the Vøring Plateau. This new scheme is intended to<br />
supercede the NRS zones provisionally proposed in the Leg 104<br />
Initial Reports. The applicability of this regional biozonation beyond<br />
the Vøring and Iceland Plateaus is not presently known.<br />
The <strong>radiolaria</strong> biostratigraphy serves as a basis for inferring a<br />
sequence of hiatuses and faunal overturns that may be associated<br />
with sea-level low stands and consequent cold-water isolation of the<br />
Norwegian Sea. Twenty-one new taxa are described as follows:<br />
Actinomma henningsmoeni, Actinomma livae, Actinomma mirabile,<br />
Actinomma plasticum, Ceratocyrtis broeggeri, Ceratocyrtis manumi,<br />
Ceratocyrtis stoermeri, Clathrospyris vogti, Corythospyris hispida,<br />
Corythospyris jubata sverdrupi, Corythospyris reuschi,<br />
Crytocapsella ampullacea, Cyrocapsella kladaros, Gondwanaria<br />
japonica kiaeri, Hexalonche esmarki, Larcospira bulbosa,<br />
Phormospyris thespios, Pseudodicytophimus amundseni,<br />
Spongotrochus vitabilis, Spongurus cauleti, and Tessarastrum<br />
thiedei.<br />
Goltman, E.B. 1989. Distribution of Upper Cretaceous<br />
deposits in southeastern Central Asia according to<br />
<strong>radiolaria</strong>ns. Dokl. Akad. Nauk Tadziksk. SSR., 32/1, 47-50.<br />
(in Russian)<br />
Gorka, H. 1989. Les Radiolaires du Campanien inférieur<br />
de Cracovie (Pologne). Acta palaeont. pol., 34/4, 327-354.<br />
Lower Campanian Radiolarians (Polycystina) from outcrops at<br />
Cracow (southern Poland) are very abundant and very well preserved,<br />
fifty species amongst spumellarians et nassellarians are described.<br />
One genus, Vistularia, and four species are new:<br />
Archaeospongoprunum cracoviense sp. n., Pseudoaulophacus<br />
polonicus sp. n., Pesudoaulophacus vistulae sp. n., and Vistularia<br />
magna gen. et sp. n.<br />
Gorka, H. & Geroch, S. 1989. Radiolarians from a<br />
lower Cretaceous section at Lipnik near Bielsko-Biala<br />
(Carpathians, Poland). Ann. Soc. geol. Pol., 59, 183-195.<br />
Radiolarians (Polycystina) from the Lower Cretaceous<br />
(Hauterivian to Albian) of Lipnik near Bielsko-Biah are redescribed.<br />
The previous determinations are revised on the basis of<br />
observations in SEM. The <strong>radiolaria</strong>ns belong to the order Spumellaria<br />
(7 species) and to Nassellaria (11 species).<br />
Gowing, M.M. 1989. Abundance and feeding ecology of<br />
Antarctic phaeodarian <strong>radiolaria</strong>ns. Marine Biol., 103, 107-<br />
118.<br />
Phaeodarian <strong>radiolaria</strong>ns were sampled from the upper 200 m<br />
along a transect through the ice-edge zone in the Weddell Sea in the<br />
austral autumn (March 1986) and at several stations in the western<br />
Antarctic Peninsula region in the austral winter (June 1987).<br />
Abundances of phaeodarians reached 3132 m -3 and were similar to<br />
or higher than maximum abundances of polycystine <strong>radiolaria</strong>ns,<br />
foraminiferans, and acantharians, and similar to or less than those<br />
of the heliozoan Sticholonche sp. Phaeodarians varied in abundance<br />
and species composition both seasonally and/or geographically. In<br />
contrast to the more numerous ciliates and flagellates that were<br />
most abundant in the upper 100 m, phaeodarians were most<br />
abundant from 100 to 200 m and showed no distinct pattern related<br />
to the ice edge. Electron microscopical examination of food vacuoles<br />
showed that phaeodarians are omnivorous generalists, feeding on a<br />
variety of food ranging in size from bacteria to large protozoans in<br />
both regions and seasons. Algal cells consumed in addition to<br />
diatoms and dinoflagellates included Chlorella-like cells and<br />
members of the recently described chrysophyte order Parmales.<br />
Scales of prasinophytes were common. Phaeodarians are consumed<br />
by the non-selective particle feeding salp Salpa thompsoni. Thus.<br />
phaeodarians link microbial food webs to macrozooplankton and<br />
increase the complexity of the Antarctic food web.<br />
Gowing, M.M. & Coale, S.L. 1989. Fluxes of living<br />
<strong>radiolaria</strong>ns and their skeletons along a northeast Pacific<br />
transect from coastal upwelling to open ocean waters. Deep-<br />
Sea Res. Part A, oceanogr. Res. Pap., 36/4, 561-576.<br />
Sinking fluxes of living polycystine and phaedorian <strong>radiolaria</strong>ns<br />
and their intact empty skeletons were measured from surface<br />
waters to 2000m using free-floating particle interceptor traps at
Radiolaria 14 Bibliography - 1989<br />
three sites ranging from highly productive coastal upwelling to<br />
oligotrophic central gyre waters in the northeast Pacific Ocean. Total<br />
<strong>radiolaria</strong>n fluxes and living phaedorian fluxes were generally highest<br />
at the coastal site throughout the water column. There was no<br />
consistent site-specific pattern for fluxes of living polycystine,<br />
polycystine empty skeletons and phaedorian empty skeletons. Living<br />
phaedorians were the only group that showed the same rank order of<br />
sites with respect to flux at both the base of the euphotic zone and<br />
at 2000m. Thus different short-term processes occurring in the<br />
water column (e.g. destructive and non-destructive predation and<br />
midwater addition of living <strong>radiolaria</strong>ns) altered <strong>radiolaria</strong>n fluxes.<br />
Neither <strong>radiolaria</strong>n fluxes at the base of the euphotic zone nor fluxes<br />
at 2000 m showed a simple correspondence with primary<br />
production, indicating that short-term measurements did not reveal<br />
long-term patterns. At most depths at all sites, fluxes of living,<br />
skeleton-bearing phaeodorians outnumbered fluxes of empty<br />
phaeodarian skeletons. In contrast, at most depths at all sites,<br />
fluxes of empty polycystine skeletons outnumbered fluxes of living,<br />
skeleton-bearing polycystine. Relatively large, living skeleton-less<br />
phaeodarians were the numerically dominant <strong>radiolaria</strong>n in the<br />
uppermost traps at the oceanic and coastal sites. These<br />
phaeodarians agglutinate siliceous skeletons of other plankton and<br />
contributed 5% of the silicoflagellate flux, 16% of the polycystine<br />
flux, and 2% of the centric diatom flux at these depths. The<br />
resemblance of skeleton-less phaeodarians to faecal pellets may<br />
cause them to be misidentified as faecal material when trap<br />
contents are dried for processing.<br />
Gowing, M.M., Garrison, D.L., Buck, K.R. &<br />
Coale, S.L. 1989. AMERIEZ 1988: winter zooplankton<br />
from the Weddell and Scotia seas. Antarct. J. U. S., 24/5,<br />
160-162.<br />
As part of the Antarctic Marille Ecosystem Research at the Ice-<br />
Edge Zone (AMERIEZ) project, we are studying the distributions,<br />
abundances, and trophic ecology of heterotrophic protozooplankton.<br />
Protozooplankton range in size from microflagellates a few<br />
micrometers in length Up to colonial <strong>radiolaria</strong>ns that can reach<br />
meters in size. In this report, we focus on protozooplankton ranging<br />
from 50 to 300 micrometers in their longest dimension. These<br />
include <strong>radiolaria</strong>ns, foraminiferans, heliozoans, and some ciliates.<br />
Samples were collected along several transects perpendicular to the<br />
ice edge during the AMERIEZ 88 cruise (see cruise track in Ainley<br />
and Sullivan, Antarctic Journal (this issue) in the austral winler from<br />
9 June to 13 August 1988. We took both quantitative plankton tows<br />
and large-volume (60-litre) water samples; this report discusses<br />
preliminary results based on analysis of water samples from 8 of 17<br />
stations. At each station, 30 litres of water were collected from<br />
each of 10 depths: 5 + 10 meters, 30 + 40) meters, 65 + 85<br />
meters, 115 + 135 meters, and 190 + 21() meters. Samples from<br />
each pair of combined depths were concentrated to 200 millilitres<br />
by reverse-flow filtration (Garrison and Buck 1989) immediately<br />
after collection and preserved with Karnovsky's fixative (Garrison<br />
and Buck 1989). Upon return to our laboratory, samples were<br />
stained with the nuclear fluorochrome DAPI (Coleman 1980),<br />
concentrated in settling chambers, and examined with an inverted<br />
fluorescence microscope. The nuclear stain allowed us to distinguish<br />
between organisms that were alive at the time of capture and empty<br />
skeletons, and also indicated organisms that were undergoing<br />
reproduction. The nuclear stain was also useful for distinguishing<br />
organisms in samples with much detritus.<br />
Gursky, H.-J. & Gursky, M.M. 1989. Thermal<br />
alteration of chert in the ophiolite basement of southern<br />
Central America. In: Siliceous Deposits of the Tethys and<br />
Pacific Regions. (Hein, J.R. & Obradovic, J., Eds.). Springer-<br />
Verlag, New York. pp. 217-233.<br />
Radiolarian chert and volcaniclastic-rich siliceous rocks of the<br />
Nicoya Complex were studied by optical mineralogy, X-ray<br />
diffractometry, and SEM. Various phenomena of thermal alteration<br />
occur due to postdepositional mafic magmatism. Progressive<br />
destruction of sedimentary features is classified into four stages<br />
from weak to complete recrystallization. Increases in quartz<br />
crystallinity reflecting diagenetic to high-grade thermo-metamorphic<br />
conditions parallel the recrystallization noted in thin sections.<br />
Mineral assemblages especially in volcaniclastic-rich rocks help<br />
estimate the metamorphic grade. Chert with smectite and illitesmectite<br />
mixed-layer minerals or heulandite and clinoptilolite,<br />
respectively, indicates low-temperature conditions of less than<br />
200°C. Piemontite, garnet, and diopside reflect low to medium or<br />
high (?) grade, very low-pressure contact metamorphism. Mineral<br />
assemblages with scapolite were found close to igneous contacts<br />
and indicate medium to high grade metamorphism. Secondary<br />
minerals in veins with dominantly barite and zeolites commonly<br />
formed under low temperature conditions of less than 150°C. These<br />
different petrologic changes are discussed as to their usefulness in<br />
defining thermal grades.<br />
- 31 -<br />
Gursky, H.J. 1989. Presencia y origen de rocas<br />
sedimentarias en el basamento ofiolítico de Costa Rica. Rev.<br />
Géol. Amér. Central, 10, 19-66.<br />
Different types of sedimentary rocks intercalated between<br />
basalts of the Nicoya Ophiolite Complex (Jurassic to Lower Tertiary,<br />
Costa Rica and western Panama) were studied using sedimentologic,<br />
petrographic, X-ray diffractional, chemical, and field methods. They<br />
occur as regionally extended sequences up to tens of meters thick,<br />
thin lenses, inter and intrapillow sediment, xenoliths, intrusive jasper<br />
bodies, tectonic blocks, and volcaniclastic material.<br />
Radiolarite sequences containing in places sedimentary<br />
manganese nodules, were formed below the CCD in the eastern<br />
equatorial Pacific Ocean under 02-rich, deep-sea conditions with<br />
little detrital input and very low-energy currents. Lenses of finegrained<br />
tuffite and detritus-rich chert were deposited in local ponds.<br />
Dikes of non-bedded jasper with colloidal structures may represent<br />
hydrothermal mineralizations or thermally mobilized radiolarite<br />
material. Lenses of pelagic foraminiferal limestone are present close<br />
to the top of the Nicoya Complex and were deposited below the CLy.<br />
Volcaniclastic breccias and sandstones represent locally-derived<br />
debris from basalt flows and fault scarps.<br />
The change from siliceous, Jurassic to middle Cretaceous, to<br />
calcareous, upper Cretaceous, sedimentation reflects the late<br />
Mesozoic world-wide lowering of the CCD and variations in regional<br />
igneous and platetectonic morphology. The data make a contribution<br />
to the reconstruction of the geodynamic evolution of the Nicoya<br />
Complex.<br />
Hattori, I. 1989a. Length-Slow Chalcedony in<br />
Sedimentary Rocks of the Mesozoic Allochthonous Terrane<br />
in Central Japan and Its Use for Tectonic Synthesis. In:<br />
Siliceous Deposits of the Tethys and Pacific Regions. (Hein,<br />
J.R. & Obradovic, J., Eds.). Springer-Verlag, New York. pp.<br />
201-215.<br />
Length-slow chalcedony was recently discovered in the<br />
Mesozoic Mino Terrane, Central Japan. Lutecite and quartzine, two<br />
varieties of length-slow chalcedony, occur in exotic limestone, chert,<br />
and dolostone blocks as secondary minerals replacing carbonates or<br />
as vein minerals. Clastic fragments of length-slow chalcedony were<br />
also found in Mesozoic turbidite sandstone in this terrane.<br />
Indigenous rock-formations carrying length-slow chalcedony have<br />
not been recognized in Japan. Length-slow chalcedony is generally<br />
considered to form under geologic environments different from<br />
those for length-fast chalcedony, that is, length-slow chalcedony<br />
tends to form in sedimentary rocks deposited on cratonic margins in<br />
arid, evaporitic environments. Accordingly, it is likely to consider<br />
that the Mino Terrane is composed of tectonic blocks and detritus<br />
from cratonic regions containing much length-slow chalcedony<br />
formed in evaporitic environments. Recent geologic, paleomagnetic,<br />
and paleontologic syntheses of the tectonic evolution of the<br />
Japanese Islands have revealed the allochthonous nature of the Mino<br />
Terrane. I suggest that length-slow chalcedony can be used as a<br />
tracer mineral to identify the provenance of the allochthonous Mino<br />
Terrane.<br />
Hattori, I. 1989b. Jurassic <strong>radiolaria</strong>ns from manganese<br />
nodules at three sites in the western Nanjo Massif, Fukui<br />
Prefecture, Central Japan. Memoirs of the Faculty of<br />
Education, Fukui University, 2/29, 47-134. (in Japanese)<br />
A number of manganese nodules occur at three localities in the<br />
Nanjo Massif, Mino Terrane, Central Japan. Generally, they are found<br />
in red shales between lower chert and upper shale and sandstone,<br />
and are considered to be rhodochrossite concretion in red shale.<br />
Abundant well-preserved <strong>radiolaria</strong>ns included in them are extracted<br />
and analyzed. They are interpreted to belong to Early to early Middle<br />
Jurassic in age. Accordingly, the manganese nodules in this area are<br />
the oldest manganese nodules in the Mino Terrane so far. For future<br />
researches, a lot of SEM photographs of <strong>radiolaria</strong>ns from the<br />
manganese nodules are presented with their distribution charts.<br />
Hattori, I. & Sakamoto, N. 1989. Geology and Jurassic<br />
Radiolarians from manganese nodules of the Kanmuriyama-<br />
Kanakusadake Area in the Nanjo Massif, Fukui Prefecture,<br />
Central Japan. Bull. Fukui municip. Mus. nat. Hist., 36, 25-<br />
79. (in Japanese)<br />
The geology of the Kanmuriyama-Kanakusadake area of the<br />
Nanjo Massif, Mino Terrane, Central Japan, is characterized by Early<br />
Jurassic olistostrome called the Kasugano Facies and Jurassic<br />
chert-sandstone facies called the Koukura Facies. Field observation<br />
suggests that the Koukura Facies structurally overlies the Kasugano<br />
Facies. Sedimentary rocks of the Koukura Facies are refolded; the<br />
fold axis of the older one was primarily of E-W direction, and the<br />
younger axis, of N-S direction. Radiolarian analysis shows that the
Bibliography - 1989 Radiolaria 14<br />
depositional ages of chert, red shale, green shale in the Koukura<br />
Facies are Middle Triassic to Early Jurassic, late Early Jurassic and<br />
Middle Jurassic, respectively. The <strong>radiolaria</strong>n age and the<br />
distribution and modes of occurrence of sedimentary rocks indicate<br />
extensive post-depositional deformation and re-arrangement of<br />
these rocks. Manganese nodules found in red shale at the west of<br />
Mt. Kanmuriyama contain abundant well-preserved late Early<br />
Jurassic <strong>radiolaria</strong>ns. By comparing the <strong>radiolaria</strong>ns in this site with<br />
the <strong>radiolaria</strong>n biostratigraphy established in the western North<br />
America, their age is considered to be Aalenian. The <strong>radiolaria</strong>ns<br />
included in manganese nodules of the Sannousan-Higashi, Sugentan-<br />
Minami, Akatani, Tarumigawa, and Kanmuriyama-Nishi sites can be<br />
said to cover the age from the middle to late Early Jurassic.<br />
Hays, P.E., Pisias, N.G. & Roelofs, A.K. 1989.<br />
Paleoceanography of the eastern equatorial Pacific during the<br />
Pliocene: a high-resolution <strong>radiolaria</strong>n study.<br />
Paleoceanography, 4/1, 57-73.<br />
Pliocene sediments from hydraulic piston cores of Deep Sea<br />
Drilling Project sites 572 and 573 in the eastern equatorial Pacific<br />
provide material for a high-resolution stratigraphic and<br />
paleoceanographic study during a period of time from 2.4 to 3.7 Ma.<br />
Radiolarian stratigraphy of these two sites reveals two major faunal<br />
events. The older event involves the gradual disappearance of five<br />
species and the appearance of three equatorial surface-dwelling<br />
<strong>radiolaria</strong>n species and occurs at the Gauss/Gilbert paleomagnetic<br />
reversal boundary which is coincident with the time of the closing of<br />
the Isthmus of Panama around 3.5 Ma [Berggren and Hollister,<br />
1974; Keigwin, 1978, 1982a, b]. The younger event involves a<br />
disappearance and appearance of two mainly Subarctic species and<br />
occurs at 2.9 Ma, prior to the onset of northern hemisphere<br />
glaciation as dated in North Atlantic sections. Analysis of<br />
quantitative <strong>radiolaria</strong>n data for extant species divides the Pliocene<br />
fauna into two assemblages which are composed of <strong>radiolaria</strong>n<br />
species that are abundant in the surface sediments of central and<br />
eastern equatorial regions. From the time series variations of these<br />
fauna, the variability of these factors has remained constant over<br />
the time interval at the eastern site but underwent a stepwise<br />
decrease at the western site. Paleotemperature transfer function<br />
techniques provided quantitative comparisons between Pliocene and<br />
Pleistocene paleooceanographic variability. At the more western<br />
site, a shift in paleotemperature estimates occurred. Using the<br />
modern day observation that the slope of the thermocline is related<br />
to the magnitude of westward wind stress, this change corresponds<br />
to an increase in wind stress. This event has been dated at about 2.8<br />
Ma and may represent an important oceanic and atmospheric<br />
precursor to the major onset of northern hemisphere glaciation at<br />
2.4 Ma. From the modem relationship between seasonal differences<br />
m temperatures at each site the Pliocene gradient in seasonality has<br />
been compared with the Pleistocene (and modem) gradients. Relative<br />
to the Pleistocene, seasonal differences in temperature were the<br />
same for the more eastern site but lower at the western site. The<br />
Pliocene gradient in seasonality was thus located farther east<br />
toward the South American continent than during the Pleistocene. No<br />
influence of the final closure of the Isthmus of Panama is seen in the<br />
extant <strong>radiolaria</strong>n data for sites 572 and 573 during the time<br />
interval from 2.4 Ma to 3.7 Ma<br />
Hein, J.R. & Obradovic, J. (Eds.) 1989a. Siliceous<br />
Deposits of the Tethys and Pacific Regions. , Springer-<br />
Verlag, New York. 244 p.<br />
Hein, J.R. & Obradovic, J. 1989b. Siliceous Deposits<br />
of the Tethys and Pacific Regions. In: Siliceous Deposits of<br />
the Tethys and Pacific Regions. (Hein, J.R. & Obradovic, J.,<br />
Eds.). Springer-Verlag, New York. pp. 1-18.<br />
This introductory chapter briefly summarizes many aspects of<br />
siliceous deposits, from the introduction of silica into the marine<br />
environment to diagenesis and evolution of depositional basins. We<br />
also describe and contrast the Mesozoic Tethyan and Pacific<br />
depositional settings of siliceous deposits. Silica enters<br />
the oceans primarily from rivers and is removed primarily in<br />
siliceous deposits via silica uptake by siliceous plankton. Less than<br />
one percent of the biogenic silica fixed in surface waters makes it<br />
into the geologic record. The solubility of the various silica<br />
polymorphs varies, and controls the dissolution or reprecipitation of<br />
silica in sea water, bottom sediments, and during late diagenetic<br />
stages. Recent studies in the geochemistry of siliceous deposits are<br />
shedding light on many long outstanding questions related to<br />
siliceous deposits. K-Ar and Rb-Sr age dating of cherts offer new and<br />
significant tools to better understand the timing of sedimentation<br />
and tectonics of chert-bearing sequences.<br />
The plate tectonic regimes and depositional basins of the<br />
Mesozoic Tethyan seaway and the circum-Pacific region were<br />
fundamentally different. These differences resulted in deposition of<br />
siliceous sequences with different lithologic associations and<br />
lithologic successions.<br />
- 32 -<br />
Hesse, R. 1989. Silica diagenesis: origin of inorganic and<br />
remplacement cherts. Earth-Sci. Rev., 26, 253-284.<br />
Silicification of originally non-siliceous sediments affects a<br />
wide variety of rock-types and materials and ranges from minor to<br />
pervasive. Partial and minor chertification occur mostly in<br />
carbonates. carbonate-bearing sandstones evaporites, and fossil<br />
wood. The source of the silica is predominantly biogenic. In petrified<br />
wood the silicification mechanism is a permeation or void-filling<br />
process, not a replacement. In this example, the sequence of silicaphase<br />
transformation is the same as that in deep-sea siliceous<br />
sediments.<br />
In many silicified rocks, particularly in certain carbonates. the<br />
transformation sequence is different from that in radiolarites or<br />
diatomites. The chemical environment and conditions of early<br />
diagenetic chert formation in shallov-water carbonates are<br />
delineated by the general mixing model of Knauth (1979), but<br />
remain unknown for most other types. An exception are the flint<br />
nodules and bands of the English Chalk. A detailed study of the<br />
paramoudra flint structures by Claylon (1986) provided remarkable<br />
insight into the replacement process.<br />
Seven different recurring silica fabrics have been recognized in<br />
chert-replaced carbonates including equigranular (microcrystalline<br />
quartz or microquartz and megaquartz) and fibrous types<br />
(chalcedony. quartzine or length-slow chalcedony, lutecite, zebraic<br />
chalcedony and microflamboyant quartz). Among the latter.<br />
quartzine and microflamboyant quartz are common in, but by no<br />
means restricted to chert-replaced evaporites, for which Milliken<br />
(1979) recognized a sequence of seven quartz-fabrics. As a single<br />
criterion, only anhydrite inclusions in megaquartz, quartzine or<br />
microllamboyant quartz provide unequivocal evidence for an<br />
evaporite precursor. The relative timing between silicification and<br />
well-established diagenetic carbonate reactions shows that virtually<br />
all theoretically possible sequences occur. Chertification of<br />
carbonate host sediment thus may take place during early,<br />
intermediate or late diagenesis, and even during<br />
anchimetamorphism.<br />
Pervasive to complete silicification has been described in<br />
lacustrine. pedogenic and hydrothermal-volcanogenic rocks and<br />
occurs on the scale of individual beds, members or entire<br />
formations. It may affect some of the aforementioned rock types<br />
too, for example carbonates. The source of the silica is<br />
predominantly inorganic. Chert formation in these environments<br />
includes direct chemical silica precipitation from solution through a<br />
gel stage. Magadi-type cherts result from the conversion of the<br />
hydrous sodium silicate magadiite into microcrystalline quartz which<br />
has occurred in East African rift valley lakes such as Lake Magadi in<br />
Late Pleistocene time. They are closely related to directly<br />
precipitated inorganic cherts which have been observed in alkaline<br />
environments of playa lakes.<br />
Silcretes originate from weathering and soil-forming processes<br />
under climatic and environmental conditions conducive to the<br />
formation of duricrusts and laterites. In more humid climates,<br />
however, non-weathering-profile silcretes occur which have been<br />
distinguished from weathering-profile silcretes. Four to five<br />
different silcrete fabric types have been established, including the<br />
(I) grain-supported (or '"quartzitic"'), (2) floating (terrazzo). (3)<br />
matrix (Albertinia and opaline), and (4) conglomeratic types.<br />
In volcanic edifices, silicification related to hydrothermal<br />
activity occurs (I) along the ascent-routes of the fluids (vents)<br />
within the volcanic complexes, (2) in isolated ponds and depressions<br />
on the sea-floor where the fluids discharge, mostly in the median rift<br />
valley of mid-ocean ridges, and (3) in geothermal areas on land<br />
associated with spreading lineaments, volcanic islands arcs,<br />
transform faults or continental hot spots. Attention has focused on<br />
the associated base-metal concentrations and less on the<br />
silicification and accompanying iron enrichment processes. The<br />
Precambrian Banded Iron Formations may be indirectly or directly<br />
related to hydrothermal-volcanic processes. The origin of these<br />
cherty iron formations certainly requires more than one genetic<br />
model and at present remains a major unresolved problem despite<br />
massive efforts to tackle it.<br />
Hollis, C. 1989. Radiolaria from K-T boundary sections in<br />
M.E. Marlborough. Geol. Soc. New Zealand, misc. Pub., 43,<br />
51.<br />
Hopkins, T.L. & Torres, J.J. 1989. Midwater food web<br />
in the vicinity of a marginal ice zone in the western Weddell<br />
Sea. Deep-Sea Res. Part A, oceanogr. Res. Pap., 36/4, 543-<br />
560.<br />
Hori, R. & Otsuka, T. 1989. Early Jurassic <strong>radiolaria</strong>ns<br />
from the Mt. Norikuradake area, Mino Terrane, central Japan.<br />
J. Geosci. Osaka City Univ., 32, 175-198.
Radiolaria 14 Bibliography - 1989<br />
This paper focuses on the late early Jurassic <strong>radiolaria</strong>n<br />
assemblage of bedded cherts and siliceous mudstones in the Mt.<br />
Norikuradake area, central Japan. Nine multi-segmented<br />
nassellarians of the assemblage including two new species, are<br />
described herein. They belong to the genera Hsuum, Parahsuum and<br />
Parvicingula and are characterised by forms possessing features of<br />
both Parahsuum and Hsuum, with also a form of Parvicingula having<br />
small tests. The assemblage containing these taxa, recognisable in<br />
various localities in Southwest Japan and North America, is regarded<br />
as a fauna of the transitional period from early Jurassic to middle<br />
Jurassic forms. This assumption is based on a consideration of the<br />
morphology of its component species. On the basis of its<br />
biostratigraphic position and faunal content, the assemblage is<br />
probably to be dated to a certain time in the late Early to early Middle<br />
Jurassic, at least including Toarcian time.<br />
Iijima, A., Kakuwa, Y. & Matsuda, H. 1989.<br />
Silicified wood from the Adoyama Chert, Kuzuh, central<br />
Honshu, and its bearing on compaction and depositional<br />
environment of <strong>radiolaria</strong>n bedded chert. In: Siliceous<br />
Deposits of the Tethys and Pacific Regions. (Hein, J.R. &<br />
Obradovic, J., Eds.). Springer-Verlag, New York. pp. 151-<br />
168.<br />
Ishida, K. 1989. Analysis of mesoscopic deformation<br />
structures in melange with special respect to the stages of<br />
syn- and post- sedimentation -A case study in the Southern<br />
Chichibu Terrane in eastern Shikoku, Southwest Japan.<br />
Struct. Geol., J. Tect. Res. Groupe Japan, 34, 95-109.<br />
Ishiga, H. 1989. Paleozoic and Mesozoic <strong>radiolaria</strong>ns<br />
fossils from Japan (Paleozoic 1-3). Atlas of Japanese fossils,<br />
66, 1-12. (in Japanese)<br />
Ishiga, H., Sugata, Y., Funakoshi, N.,<br />
Takeshita, H. & Tokuoka, T. 1989. Biostratigraphy<br />
and structure of the Permian Maizuru Group in western part of<br />
Okayama Prefecture, Southwest Japan with special reference<br />
to acid volcanic rocks. Geol. Rep. Shimane Univ., 8, 61-71.<br />
(in Japanese)<br />
The Permian rocks in the Ibara and Bisei areas. western part of<br />
Okayama Prefecture consist of sedimentary complex rock units,<br />
comprising the Maizuru Group of the Maizuru Terrane and the rocks<br />
of the Ultra-Tamba Terrane. The complex of the Maizuru Group in the<br />
Ibara area is divided into the following 5 units (unit A. B. C. D and E in<br />
apparently ascending order) on the basis of lithology. composition,<br />
age and structure.<br />
The unit A mainly consists of acid volcanic and volcaniclastic<br />
rocks and intercalated with mudstones. sandstones and<br />
conglomerates. The ophiolite occurs in mudstones of the unit A.<br />
The unit B is composed chiefly of mudstone including blocks of<br />
basic volcanic rocks accompanying bedded cherts.<br />
The unit C is Yakuno ophiolite, mainly consists of metabasalts<br />
(MORB-like tholeiite) with metagabbro and ultramafic rocks.<br />
The unit D consists of basic volcanic rocks and intercalated<br />
with bedded cherts and mudstones.<br />
The unit E of the Ultra-Tanba Tarrane is composed of alternated<br />
beds of sandstones and mudstones. which are strongly sheared. The<br />
units E. F and K are discriminated in the Bisei area.<br />
The unit F consists of acid volcanic and volcaniclastic rocks<br />
and intercalating mudstones and sandstones. which corresponds to<br />
those of the unit A in the Ibara area. The unit K is composed of the<br />
Kurohagi Formation mainly of mudstones yielding late Middle<br />
Permian <strong>radiolaria</strong>ns. The mudstone includes acid volcanic rocks, and<br />
intruded by acidic dykes.<br />
Based on the <strong>radiolaria</strong>n biostratigraphy and above evidence<br />
especially occurrence of acid volcanic rocks and ophioiitic breccias<br />
in the Maizuru Terrane. it could be inferred that a rifted-ophilite<br />
assemblage of Early Permian age and acid volcanic rocks of late<br />
Middle Permian age represent a fragment of back arc basin and<br />
island arc.<br />
Isozaki, Y. & Nishimura, Y. 1989. Fusaki Formation,<br />
Jurassic subduction-accretion complex on Ishigaki Island,<br />
southern Ryukyus and its geologic implication to Late<br />
Mesozoic convergent margin of East Asia. In: High-pressure<br />
metamorphic belts and tectonics of the inner zone of<br />
southwestern Japan. (Nishimura, Y. et al., Eds.), vol. 33.<br />
- 33 -<br />
Memoirs of the geological Society of Japan, pp. 259-275.<br />
(in Japanese)<br />
Present study on the weakly metamorphosed pre-Tertiary rocks<br />
(Fusaki Formation) on Ishigaki Island, southern Ryukyus has brought<br />
new information concerning their tectono-sedimentary history as<br />
follows. 1 ) The weakly metamorphosed rocks form a sedimentary<br />
complex of olistostromal aspect, mostly dominated by pebbly<br />
mudstone. It contains abundant allochthonous blocks and lenses of<br />
sandstone, mudstone, chert, limestone, and so on. 2 ) Microfossils<br />
such as conodonts, <strong>radiolaria</strong>ns and smaller foraminifers were newly<br />
found out, providing age assignment for the exotic blocks and<br />
lenses. Namely, the olistostromal complex contains Permian<br />
limestone, Permian ( + Pennsylvanian?) and Triassic bedded cherts<br />
and Early Jurassic siliceous mudstone. 3) Sandstone sills and dykes<br />
intruded into the allochthonous blocks, indicating that these chaotic<br />
sedimentary rocks were mixed before the consolidation of coarsegrained<br />
clastic rocks. Judging from these results, the weakly<br />
metamorphosed rocks are inferred to be a subduction-related<br />
sedimentary complex formed in trench environs during the Middle<br />
Jurassic, and are best compared with the Jurassic complex in<br />
Southwest Japan, which is interpreted as an ancient subductionaccretion<br />
complex along the eastern margin of Jurassic Asia.<br />
On the other hand, previous studies have revealed that high P/T<br />
metamorphic rocks with 240-160 Ma K-Ar ages (Tomuru Formation)<br />
tectonically overlie upon the Fusaki Formation, and that they are<br />
correlated to the Sangun metamorphic rocks in Southwest Japan.<br />
Thus the pair of the high P/T metamorphic, rocks and the weakly<br />
metamorphosed olistostromal complex on Ishigaki Island, southern<br />
Ryukyu Arc, is compared with that of the Sangun metamorphic rocks<br />
and adjacent Jurassic olistostromal complex (liuga Group) in the<br />
Inner Zone of Southwest Japan. In other words, the southern Ryukyu<br />
Arc is regarded as a southwestern extension of the Inner Zone of<br />
Southwest Japan. while the northern Ryukyu Arc is surely a<br />
southwestern extension of the Outer Zone. It is suggested,<br />
therefore, that the northern and southern Ryukyu Arcs are offset in<br />
left-lateral manner along the Kerama Gap, and that the width of the<br />
Outer Zone becomes considerably narrower south-westward on the<br />
south of Ishigaki Island. Concerning the Jurassic complex along the<br />
eastern margin of Asia, its lateral extension is probably traced from<br />
the Nadanhada area on China/USSR border to west Philippines<br />
(probably further to west Borneo) via Japanese Islands, and the<br />
Jurassic complex on Island gives a missing link in this organic chain<br />
between Southwest Japan and North Palawan. west Philippines. The<br />
boundary thrust between the Jurassic complex and the overlying pre-<br />
Jurassic orogenic complexes, newly designated as the Ishigaki-Kuga<br />
Tectonic Line in this paper, can be also traced along this trend in<br />
East Asia.<br />
Isozaki, Y. & Tamura, H. 1989. Late Carboniferous and<br />
Early Permian <strong>radiolaria</strong>ns from the Nagato tectonic zone and<br />
their implication to geologic structure of the Inner Zone,<br />
southwest Japan. In: High-pressure metamorphic belts and<br />
tectonics of the inner zone of southwestern Japan.<br />
(Nishimura, Y. et al., Eds.), vol. 33. Memoirs of the<br />
geological Society of Japan, pp. 167-176. (in Japanese)<br />
Ages of some undated sedimentary rocks in the Nagato<br />
Tectonic Zone in the western Chugoku district, Southwest Japan,<br />
were examined by virtue of <strong>radiolaria</strong>n biostratigraphy. The newly<br />
obtained microfossil data strongly support the recent understanding<br />
that the Nagato Tectonic Zone is continuous with the Hida Marginal<br />
Zone in central Japan, in conjunction with the occurrence of coeval<br />
high P/T schist in both zones. Late Carboniferous <strong>radiolaria</strong>ns were<br />
found out from an andesitic tuffaceous mudstone of a sedimentary<br />
unit previously called "undated Paleozoic formation in the Dai area,<br />
Mine City. Such kind of andesitic tuffaceous mudstone is not known<br />
at all in the Chugoku district but in the Hida Marginal Zone. This unit<br />
is newly designated as the Higashi-hirano Formation.<br />
Early Permian <strong>radiolaria</strong>ns were found out from an<br />
allochthonous block of bedded chert, which is contained in coarsegrained<br />
clastic rocks called the Toyohigashi Group in the Toyogadake<br />
area. Toyota-cho. Judging from the age and mode of occurrence of<br />
the chert block. and the total lithologic- assemblage of the unit, this<br />
group can be properly correlated with the Middle-Late Permian<br />
accretionary complex of the Akiyoshi Belt, which is distributed not<br />
merely in the east of the Nagato Tectonic Zone but also in the Hida<br />
Marginal Zone.<br />
Iturralde-Vinent, M.A. 1989. Role of ophiolites in the<br />
geological structure of Cuba. Geotectonics, 23/4, 332-342.<br />
Iwasaki, T., Sashida, K. & Igo, H. 1989. Mesozoic<br />
strata of the Kitaaiki-Kawakami area in Minamisaku County,<br />
Nagano prefecture, northwest Kanto mountains, central<br />
Japan. J. geol. Soc. Japan, 95/10, 733-753. (in Japanese)
Bibliography - 1989 Radiolaria 14<br />
The stratigraphy and ages of Mesozoic strata of the Kitaaiki-<br />
Kawakami area in Minamisaku County, Nagano Prefecture, central<br />
Japan are discussed based on recent fossil findings. The geology of<br />
this area is subdivided into two, namely, the eastern and western<br />
parts by the Shiraiwa-Kurio Fault trending NNE-SSW direction. The<br />
Mesozoic strata of the eastern part are subdivided into the following<br />
belts from north to south the Kijihara, Ogurayama, Tenguyama, and<br />
Kawakami Belts; and in the western part, into Kijihara, Ogurayama,<br />
Tenguyama and Kappazaka Belts. Each belt is in contact with<br />
northward-dipping reverse faults. The strata of each belt are<br />
composed mainly of chaotic rocks consisting of exotic blocks in a<br />
shaly matrix. Based on <strong>radiolaria</strong>ns extracted from shaly matrix, the<br />
strata of this area are newly classified as the Early to Middle<br />
Jurassic Kijihara Formation, the late Early Jurassic to Early<br />
Cretaceous Ogurayama Formation, Middle to Late Jurassic<br />
Tenguyama Formation, the Late Jurassic to late Early Cretaceous<br />
Kawakami Formation and late Middle Jurassic to Latest Jurassic<br />
Kappazaka Formation, and the southward younging of shaly matrix is<br />
recognized. The Butsuzo Tectonic Line in the present area is<br />
represented by the Kawakami Fault which is traceable along the<br />
Maekawa River and borders the Kawakami Formation and the<br />
Masutomi Group. The Torinosu Limestone embedded in dark green<br />
shale of the Kappazaka Formation is considered as exotic blocks.<br />
Mesozoic strata of this area were formed by accretionary process of<br />
oceanic plate up to late Early Cretaceous.<br />
Iwata, K. & Tajika, J. 1989. Jurassic and Cretaceous<br />
<strong>radiolaria</strong>ns from the pre-Tertiary system in the Hidaka Belt,<br />
Maruseppu region, Northeast Hokkaido. J. Fac. Sci.<br />
Hokkaido Univ., 22/3, 453-466.<br />
We have made a study of the pre-Tertiary Hidaka Supergroup<br />
(the Kanayama Formation), which is distributed at the most easterly<br />
portion of the Hidaka Belt, in order to ascertain the age of<br />
accumulation of this supergroup. The Kanayama Formation consists<br />
mainly of broken formations in which clastic rocks of terrigenous<br />
origin predominate and many exotic blocks are included in the scaly<br />
shale matrix. The tuffaceous shale of this formation yielded<br />
Amphipyndax tylotus—Clathrocyclas diceros <strong>radiolaria</strong>n assemblage<br />
which indicates late Campanian to early Maastrichtian age. And a<br />
late Jurassic Stylocapsa (?) spiralis and early Cretaceous<br />
Sethocapsa trachyostraca—Staurosphaera septemporatus<br />
assemblages were obtained from chert block within the melange<br />
facies of the Kanayama Formation. This formation may represent a<br />
part of accretionary complex formed by subduction process during<br />
the late Cretaceous.<br />
Johnson, D.A., Schneider, D.A., Nigrini, C.A.,<br />
Caulet, J.P. & Kent, D.V. 1989. Pliocene-Pleistocene<br />
<strong>radiolaria</strong>n events and magnetostratigraphic calibrations for<br />
the tropical Indian Ocean. Mar. Micropaleontol., 14/1-3, 33-<br />
66.<br />
A composite of four piston cores from the Central Indian Basin<br />
and adjacent Ninetyeast Ridge has yielded a continuous<br />
magnetobiostratigraphic reference section for most of the Pliocene<br />
and the Pleistocene (0.0-4.5 Ma). We identified thirty-three<br />
<strong>radiolaria</strong>n events (first- or last-occurrences ), and precisely<br />
correlated each event to the Neogene geomagnetic polarity time<br />
scale. Thirteen of these events are based on revised taxonomic<br />
studies of the genera Anthocyrtidium and Pterocorys. Some events<br />
show significant departures from synchroneity: five of the<br />
<strong>radiolaria</strong>n first-appearances and seven of the last-appearances are<br />
time-transgressive by 0.4 m.y. or greater. We here propose a<br />
revised, eleven-fold <strong>radiolaria</strong>n zonation for the Pliocene-<br />
Pleistocene, using zonal boundaries defined by events which are<br />
easily recognized and are demonstrably synchronous in the tropical<br />
Indo-Pacific. The sequence of faunal and floral events reported in<br />
this paper will allow high-resolution biostratigraphic correlations<br />
within the tropical Indian Ocean; however, the same sequence of<br />
events is not necessarily applicable to other tropical or extratropical<br />
regions.<br />
Jud, R. 1989. Lower Cretaceous <strong>radiolaria</strong>n biostratigraphy<br />
in Umbria and southern Alps. In: 1st Meeting of the working<br />
group 2; Abstracts book. (Coccioni, R., Monechi, S. &<br />
Parisi, G., Eds.). IGCP Project n. 262, Urbino, Italy. pp. 45-<br />
48.<br />
Kamon, M. & Nakazawa, K. 1989. Geology of the<br />
southern Chichibu Belt in the eastern part of Shimizu-cho,<br />
Wakayama Prefecture, southwestern Japan. J. geol. Soc.<br />
Japan, 95/1, 45-61. (in Japanese)<br />
Karl, S.M. 1989. Paleoenvironmental Implications of<br />
Alaskan Siliceous Deposits. In: Siliceous Deposits of the<br />
- 34 -<br />
Tethys and Pacific Regions. (Hein, J.R. & Obradovic, J.,<br />
Eds.). Springer-Verlag, New York. pp. 169-200.<br />
Kashima, N. & Takahashi, J. 1989. Geology and<br />
<strong>radiolaria</strong>n age of the three aqueduct tunnels (Takagushi,<br />
Tokunomori and Kanayama) at the Shimanto Belt, western<br />
Shikoku, Japan; geological studies of the construction of the<br />
aqueduct tunnels for government-operated Nanyo Irrigation<br />
Project; Part 5. Mem. Ehime Univ. nat. Sci., Ser. D (Earth<br />
Sci.), 11/1, 15-29. (in Japanese)<br />
Kato, Y. & Iwata, K. 1989. Radiolarian biostratigraphic<br />
study of the pre-Tertiary system around the Kamikawa Basin,<br />
central Hokkaido, Japan. J. Fac. Sci. Hokkaido Univ., 22/3,<br />
425-452.<br />
A re-investigation on the pre-Tertiary System that lies within<br />
the Kamikawa Basin, central Hokkaido, was carried out from a<br />
<strong>radiolaria</strong>n biostratigraphic point of view. As a result, Tosshozan<br />
Formation and the Toma Formation, which have been previously<br />
included in the Sorachi Group and regarded as Triassic and Permian-<br />
Triassic sequences respectively, are now seen to consist of<br />
olistostromes of the Early Cretaceous age (Berriasian ?-Valanginian<br />
in the former formation and Barremian to Aptian in the latter<br />
formation). The Toma Formation in particular includes many exotic<br />
blocks of various geological ages: middle Permian and late Triassic<br />
limestones, late Triassic chert, late Jurassic chert and limestones,<br />
siliceous shales or acidic tuffs of Early Cretaceous, and sandstones<br />
and greenstones. The matrix of this formation consists of pebbly<br />
shale which is strongly sheared. A similar oliststrome belt of early<br />
Cretaceous age extends from the western flank of the southern<br />
Hidaka Belt to Sakhalin and seems to represent a convergent zone<br />
along the Eurasian plate margin during the early Cretaceous time.<br />
Additionally, we have found that the Takasu and the Kaimei<br />
Formations in the studied region belong to the Middle Yezo<br />
Supergroup, while the Hidaka Supergroup is here represented by the<br />
Aibetsu Formation belonging to the late Cretaceous sequence.<br />
Consequently, we proposed a revision of stratigraphy of the Pippu—<br />
Toma regions.<br />
Kimbrough, D.L. 1989. Franciscan Complex rocks on<br />
Cedros Island Baja California Sur, Mexico; <strong>radiolaria</strong>n<br />
biostratigraphic ages from a chert melange block and<br />
petrographic observations on metasandstone. In: Geological<br />
studies in Baja California, Field Trip Guidebook. (Abbot,<br />
P.L., Eds.), vol. 63. Pacific Section, Society of economic<br />
Paleontologists and Mineralogists, pp. 103-107.<br />
Kito, N. 1989. Radiolaires du Jurassiques Moyen et<br />
Supérieur de Sicile (Italie): Biostratigraphie et Taxonomie.<br />
Ph.D. Thesis. Mém. Sci. Terre Univ. Curie, Paris, n. 89-7,<br />
239 p.<br />
This work is devoted to biostratigraphic and taxonomic studies<br />
of Jurassic }<strong>radiolaria</strong>ns from two sections of Sicily. One of the two<br />
sections, the Contrada La Ferta section, yields 182 species in which<br />
74 species are new, and the other section, the Galati section,<br />
yielded 41 species in which 7 species are new.<br />
The assemblages of these two sections are correlated with<br />
previously proposed biostratigraphic zonations, and the ages are<br />
estimated by the correlations and by concurrent range zones of the<br />
species. Based on the analysis, the Contrada La Ferta section is<br />
assigned from Middle Jurassic (Aalenian/Bajocian) to Upper<br />
Jurassic/Lower Cretaceous (Tithonian/Berriasian), and Galati<br />
section is assigned to Upper Jurassic (Kimmeridgian/Oxfordian). The<br />
ages obtained by different zonations are not exactly concordant<br />
each other for Middle Jurassic. On the contrary, the ages for Late<br />
Jurassic are relatively concordant. The work showed, on the other<br />
hand, that the stratigraphic ranges of many species known from Late<br />
Jurassic are enlarged into Middle Jurassic, and stratigraphic ranges<br />
of certain taxa known from Early and Middle Jurassic are enlarged<br />
into Late Jurassic. Many new species were found from the Middle<br />
Jurassic, and the fauna of the period is distinct from Early and Late<br />
Jurassic faunas.<br />
The phylogeny of Hagiastridae was analysed by the cladistic<br />
methods of cladism. Sixteen characters were analysed based on<br />
recognition of homology. After the comparison between the<br />
phylogeny and the stratigraphic ranges, generally, more the<br />
structure is complex, later the first occurrence is, but it is not<br />
always the same. Certain taxa of simple structure are later than<br />
more complex taxa. It means that the stratigraphic range does not<br />
always assure the genealogical precedence. The classification of<br />
Hagiastridae was revised based on the reconstructed phylogeny.<br />
According to the new classification, the family Hagiastridae (s.s.) is<br />
composed of 2 subfamily, 3 tribes, 4 subtribes and of 16 genera.<br />
Some existent taxa of Hagiastridae are polyphyletic or paraphyletic
Radiolaria 14 Bibliography - 1989<br />
which are not appropriate for phylogenetic classification. These<br />
polyphyletic and paraphyletic taxa are redefined to be monophyletic.<br />
On the other hand, the analysis shows some parallelisms which are<br />
relatively frequent in Hagiastridae, and the analyse defined the<br />
universality level of characters.<br />
Kojima, S. 1989. Mesozoic terrane accretion in Northeast<br />
China, Sikhote-Alin and Japan regions. Palaeogeogr.<br />
Palaeoclimatol. Palaeoecol., 69, 213-232.<br />
The Nadanhada Range in Northeast China is composed of upper<br />
Paleozoic limestone, greenstone, middle to late Triassic bedded<br />
chert, and middle Jurassic siliceous shale; these rocks are enclosed<br />
in post-middle Jurassic clastic rocks. The lithologic association,<br />
ages, <strong>radiolaria</strong>n assemblages and geologic structure of the<br />
Nadanhada Range are very similar to those of the Tamba Mino-Ashio<br />
terrane in Southwest Japan. This indicates that the Nadanhada Range<br />
is the northern extension of the Tamba Mino-Ashio terrane.<br />
Mesozoic tectonostratigraphic terranes identified in Northeast<br />
China, Sikhote-Alin and Southwest Japan are: the Khanka terrane (a<br />
micro-continent composed of Precambrian metamorphic rocks and<br />
Paleozoic to Mesozoic sedimentary and volcanic covers), the<br />
Nadanhada Western Sikhote-Alin terrane (a disrupted terrane<br />
composed of upper Paleozoic to Jurassic sedimentary rocks), the<br />
Eastern Sikhote-Alin terrane (a terrane composed mainly of early<br />
Cretaceous clastics), the Tetyukhe terrane (a disrupted terrane<br />
composed of upper Paleozoic to early Cretaceous sedimentary<br />
rocks), the Hida terrane (a continent-type stratigraphic terrane<br />
composed of Precambrian and upper Paleozoic basement covered<br />
with Jurassic to Cretaceous coarse clastics), and the Tamba Mino<br />
Ashio terrane (a disrupted terrane composed of upper Paleozoic to<br />
earliest Cretaceous sedimentary rocks). Accretionary history of<br />
these terranes is discussed on the basis of paleomagnetic and<br />
paleobiogeographic data.<br />
Kojima, S., Mizutani, S., Nagai, H., Saito, M.,<br />
Tsukamoto, H. & Yogo, M. 1989. Design and<br />
utilization of the data base system for <strong>radiolaria</strong>n fossils in<br />
the Nagoya University Museum. Bull. Nagoya Univ.,<br />
Furukawa Mus., spec. Rep., 1, 1-192.<br />
The data base system is designed for the collection of<br />
<strong>radiolaria</strong>n fossils in the Nagoya University Museum, which includes<br />
(1) <strong>radiolaria</strong>n fossils mounted on the SEM holders, (2) rock<br />
specimens from which the <strong>radiolaria</strong>n fossils are extracted, (3) JMP<br />
cards (locality description cards), and (4) <strong>radiolaria</strong>n<br />
photomicrographs and their negative films. The number of the<br />
photomicrographs attains to 50,000 at the end of 1988.<br />
Alphanumeric data concerned with these materials, such as register<br />
number, photograph number, SEM holder number, fossil positioning<br />
number on the holder, JMP card number, rock specimen number,<br />
lithology of rock specimen, locality name, and name of person who<br />
extracts the fossil, are recorded for each photomicrograph in 144<br />
bytes memory space of the Nagoya University Computation Center<br />
(NUCC); part of the data are coded and others are written in a free<br />
format. A software package is developed for inputting, listing and<br />
retrieving these data. Personal computers (PC9801 series of NEC<br />
Co.) and software (The CARD2 of ASCII Co.) are employed for<br />
personal use of the data, and the utility programs for data<br />
conversion and data transmission between the data of the NUCC and<br />
those of the Personal computers are developed. Manuals and original<br />
programs of this data base system are also described.<br />
Kolar-Jurkovsek, T. 1989. New Radiolaria from the<br />
Ladinian substage (Middle Triassic) of Slovenia (NW<br />
Yugoslavia). N. Jb. Geol. Paläont., Mh., 3, 155-165.<br />
From the Ladinian beds of Slovenia are described Bogdanella n.<br />
g. and seven new species of <strong>radiolaria</strong>: Pseudostylosphera slovenica<br />
n. sp., P. sudari n. sp., Sepsagon ? aequispinosus n. sp., Pterospongus<br />
bogdani n. sp., Bogdanella trentana n. g. n. sp., Pentaspongodiscus<br />
julicus n. sp. and Praeheliostaurus undulatus n. sp.<br />
Konstantinovskaya, Y.A. 1989. Exotic sedimentary<br />
breccias of the Ozernoy Peninsula (East Kamchatka) and their<br />
tectonic significance. Geotectonics, 23/5, 451-455.<br />
Kozur, H. & Mostler, H. 1989. Radiolarien und<br />
schwammsleren aus dem Unterperm des Vorurals. Geol.<br />
Pälont. Mitt. Innsbruck, 2, 147-275.<br />
Rich <strong>radiolaria</strong>n faunas are described from the Sarabil<br />
Formation (Upper Tastubian, higher part of Lower Sakmarian) and<br />
from the Koshelev Formation (basal part of Upper Kungurian) of the<br />
Cis-Ural. Many well preserved sponge spicules which are present in<br />
the Sarabil Formation are described as well. The Sakmarian<br />
<strong>radiolaria</strong>n and sponge faunas are well dated by ammonoids and<br />
conodonts. Also the Koshelev Formation yielded ammonoids and<br />
- 35 -<br />
conodonts, placed into the Kungurian by all workers of these fossil<br />
groups. NAZAROV & ORMISTON (1985) placed the Koshelev<br />
Formation without paleontological evidences into the Late<br />
Artinskian. Therefore the stratigraphic position of the Koshelev<br />
Formation had to be discussed in detail. In the <strong>radiolaria</strong>n taxonomic<br />
part some general problems of the taxonomy of Paleozoic<br />
<strong>radiolaria</strong>ns are discussed on concrete examples. 7 families, one<br />
subfamily, 19 genera, 2 subgenera, 36 species and 3 subspecies<br />
are established and several formerly described taxa are revised.<br />
Moreover, the Carboniferous and Permian Albaillellacea and the<br />
Permian Ruzhencevispongacea are revised in detail. 9 <strong>radiolaria</strong>n<br />
zones and associations could be discriminated within the time<br />
interval from the uppermost Carboniferous up to the Kungurian of<br />
the Cis-Ural. This Zonation is mainly based on the development<br />
within the Ruzhencevispongacea, but also Albaillellacea and<br />
Entactinaria have been used for this zonation. The Tethyan Permian<br />
could be subdivided into 16 <strong>radiolaria</strong>n zones. They are mainly based<br />
on the rather rapid phylomorphogenetic changes within the<br />
Albaillellacea. Some stratigraphic importance have here also highly<br />
specialized representatives of the Ruzhencevispongacea<br />
(Spumellaria) and some highly specialized Entactinaria. The majority<br />
of the frequent Permian Entactinaria and of the mostly subordinate<br />
Permian Spumellaria are long-living facies fossils that can be used<br />
only for coarse stratigraphic subdivisions. The siliceous spicules<br />
were investigated systematically to reconstruct the sponges being<br />
involved in the composition of the Lower Permian sediments. Within<br />
the 52 types of spicules 13 unknown specimens were found. Within<br />
the 8 orders of Demospongea 5 orders were provable. Lithisthida are<br />
the best represented ones. Within the Hexactinellida Reticulosida as<br />
well as Hexactinosida and Hemidiscosida are respresented. It is<br />
remarkable that the latter ones are far dominating compared with<br />
the Reticulosida. This is to show that many sponges of the<br />
Retticulosida have already become extinct in the Lower Permian and<br />
that they did not reach up to the Permian/Triassic boundary, as<br />
often postulated caused by ignorance about stratigraphy.<br />
Kruglikova, S.B. 1989. Arctic Ocean Radiolarians. In:<br />
The Arctic Seas: climatology, oceanography, geology<br />
andbiology. (Herman, Y., Eds.). Van Nostrand Reinhold, New<br />
York, USA. pp. 461-479.<br />
Radiolaria are unicellular planktonic animals inhabiting all<br />
oceans and seas with lower salinities from 32-38‰ . There is no<br />
record of their occurrence in seas with lower salinity (the Black,<br />
Baltic, and Beloye seas); in near-shore regions the <strong>radiolaria</strong>n<br />
abundance and diversity drop sharply. The vertical distribution of<br />
Radiolaria ranges from surface to abyssal depths with maximum<br />
number of species between 0 m and 200-300 m.<br />
Until recently Radiolaria included all marine protozoans<br />
possessing the characteristic intracellular structure the central<br />
capsule. The <strong>radiolaria</strong>n group includes the Acantharia, the<br />
Spumellaria, the Nassellaria, the Phaeodaria, and the Sticholonchea.<br />
The acantharian skeleton is composed of strontium sulphate and the<br />
Phaeodarian possess siliceous shells With a large admixture of<br />
organic material. The skeletons of Acantharia and the majority of<br />
Phaeodarian dissolve immediately after the cell dies and do not<br />
reach the seafloor. Bottom sediments yield rare Phaeodarian species<br />
belonging to the genera Cadium, Challengeria, Euphysetta, and<br />
Protocystis. Generally sediments contain Spumellaria and<br />
Nassellaria almost exclusively (Polycystina); they possess siliceous<br />
(opaline) skeletons. Spumellaria is represented by single and colonial<br />
organisms (Collosphaerida). Consequently, in the description of<br />
bottom sediments the term Radiolaria refers only to Polycystina; ill<br />
the analysis of <strong>radiolaria</strong>n data obtained from plankton samples our<br />
attention shall be centered on <strong>radiolaria</strong>ns. Due to the morphological<br />
features and chemical composition, Acantharia are at present<br />
separated from the typical Radiolaria as a kindred but separate<br />
group. The classification of Stycholonchea as Radiolaria is now<br />
dubious (Petrushevskaya 1981; Anderson, 1983).<br />
Kruglikova, S.B. 1989. Certain aspects of <strong>radiolaria</strong>n<br />
data as evidence of the paleoenvironment. Palaeogeogr.<br />
Palaeoclimatol. Palaeoecol., 69/1-2, 303-320.<br />
Different aspects of the ecology and biogeography of<br />
<strong>radiolaria</strong>ns are considered as a means of interpreting the<br />
paleoenvironment. The quantitative and spatial distribution of<br />
<strong>radiolaria</strong>ns in the sediments of the world ocean are discussed,<br />
including differences between marine and oceanic thanatocoenoses,<br />
relations between species and high rank associations of <strong>radiolaria</strong>ns<br />
and fluctuation of climate, areal changes of some species with time,<br />
etc.<br />
Kurimoto, C. 1989. Microfossil from the Gozaishoyama<br />
district in the southwestern part of the Mino Terrane, cental<br />
Japan. Bull. geol. Surv. Japan, 40/2, 55-64. (in Japanase)<br />
About 160 samples of mudstone, siliceous mudstone and chert<br />
were collected to extract microfossils from the Gozaishoyama
Bibliography - 1989 Radiolaria 14<br />
district in the southwestern part of the Mino Terrane. As a result,<br />
<strong>radiolaria</strong>ns and conodonts available for age-determination were<br />
obtained from 8 samples. Radiolarian assemblages from mudstone<br />
are correlated with those of early Late Jurassic (1 sample), late<br />
Middle Jurassic (1 sample) and Jurassic ages (4 samples). Conodont<br />
from one of 2 chert samples is correlated with that of Late Triassic<br />
age and <strong>radiolaria</strong>n assemblage from another chert sample is of<br />
Middle to Late Permian age.<br />
Of the above-mentioned data, early Late Jurassic <strong>radiolaria</strong>ns<br />
are the youngest in the fossils ever obtained from the sandstonechert<br />
facies which are situated in the inner (northern or<br />
northwestern) side of the line of the greenstone-limestone facies.<br />
Lazarus, D. & Pallant, A. 1989. Oligocene and<br />
Neogene <strong>radiolaria</strong>ns from the Labrador Sea, ODP Leg 105.<br />
In: Proceedings of the Ocean Drilling Program, Scientific<br />
Results. (Srivastava, S.P., Arthur, M., Clement, B. et al.,<br />
Eds.), vol. 105. College Station, TX (Ocean Drilling<br />
Program), pp. 349-380.<br />
Two sites in the Labrador Sea and one site in Baffin Bay were<br />
drilled during Leg 105. Radiolarians were recovered at all three sites,<br />
although at Site 645 (Baffin Bay), <strong>radiolaria</strong>ns were present in useful<br />
numbers only in the mudline sample. Radiolarians of late Neogene age<br />
were recovered at Site 646 south of Greenland, while early Oligocene<br />
and early Miocene <strong>radiolaria</strong>ns were recovered from the Labrador Sea<br />
at Site 647. In Site 646, <strong>radiolaria</strong>n and other coarse-fraction<br />
abundances vary dramatically from sample to sample and may<br />
reflect deep-water depositional processes as well as changes in<br />
surface-water conditions. Site 647 siliceous microfossils reach their<br />
peak abundance and preservation in Core 105-647A-25R and<br />
decline gradually upward into the lower Miocene (Cores 105-647A-<br />
13R and -14R). Siliceous microfossil abundances in counts of the<br />
>38-µm carbonate-free coarse fraction from the siliceous interval<br />
are correlated to each other, but not to the abundance of nonbiogenic<br />
coarse-fraction components. Radiolarian abundances in specimens<br />
per gram (but not diatom abundances) are correlated to bulk opal<br />
concentration and to the organic carbon content of the sediment. The<br />
abundance of <strong>radiolaria</strong>ns and other siliceous microfossils within the<br />
lower Oligocene to lower Miocene is interpreted as reflecting<br />
changes in surface-water productivity. With only a few exceptions,<br />
no stratigraphic indicator species were seen in samples from either<br />
Site 646 or Site 647. The absence of both tropical/subtropical and<br />
Norwegian-Greenland Sea stratigraphic forms is due to the<br />
dominance of subarctic North Atlantic taxa in Leg 105 assemblages.<br />
The early Oligocene and early Miocene assemblages recovered at<br />
Site 647 are of particular interest, as very little material of these<br />
ages has previously been recovered from the subarctic North<br />
Atlantic region, and virtually no descriptive work has been conducted<br />
on the more endemic components of the <strong>radiolaria</strong>n assemblages<br />
from these time intervals. Thus, this report concentrates on<br />
providing, at least in part, the first comprehensive documentation of<br />
early Oligocene and early Miocene <strong>radiolaria</strong>ns from the subarctic<br />
North Atlantic, with emphasis on basic descriptions, measurements,<br />
and photographic documentation. However, synonymic work and<br />
formal designation of new species names has been deferred until<br />
additional material from other regions can be examined. The sole<br />
exception is the emendation of Theocalyptra tetracantha Bjørklund<br />
and Kellogg 1972 to Cycladophora tetracantha n. comb.<br />
Maliva, R.G., Knoll, A.H. & Siever, R. 1989.<br />
Secular Change in chert distribution: A reflection of Evolving<br />
Biological Participation in the silica cycle. Palaios, 4, 519-<br />
532.<br />
In the modern oceans, the removal of dissolved silica from sea<br />
water is principally a biological process carried out by diatoms, with<br />
lesser contributions from Radiolaria, silicoflagellates, and sponges.<br />
Because such silica in sediments is often redistributed locally during<br />
diagenesis to form nodular or bedded chert, stratigraphic changes in<br />
the facies distribution of early diagenetic chert provide important<br />
insights into the development of biological participation in the silica<br />
cycle. The abundance of chert in upper Proterozoic peritidal<br />
carbonates suggests that at this time silica was removed from<br />
seawater principally by abiological processes operating in part at the<br />
margins of the oceans. With the evolution of demosponges near the<br />
beginning of the Cambrian Period, subtidal biogenic cherts became<br />
increasingly common, and with the Ordovician rise of Radiolaria to<br />
ecological and biogeochemical prominence, sedimented skeletons<br />
became a principal sink for oceanic silica. Cherts of Silurian to<br />
Cretaceous age share many features of facies distribution and<br />
petrography but they differ from Cenozoic siliceous deposits. These<br />
differences are interpreted to reflect the mid-Cretaceous radiation<br />
- 36 -<br />
of diatoms and their subsequent rise to domination of the silica<br />
cycle. Biogeochemical cycles provide an important framework for the<br />
paleobiological interpretation of the organisms that participate in<br />
them.<br />
Martini, R., De Wever, P., Zaninetti, L.,<br />
Danelian, T. & Kito, N. 1989. Les Radiolarites<br />
triasiques de la Formation du Monte Facito Auct. (Bassin de<br />
Lagonegro, Italie Méridionale). Rev. Paléobiol., 8/1, 143-<br />
161.<br />
Middle Triassic (Anisian-Ladinian) radiolarites are described for<br />
the first time in the lower part of the Lagonegro II Unit (Monte Facito<br />
Auct. Formation). Analysis of radiolarite composition and variation<br />
of the major chemical elements indicates:<br />
- a biological origin for the silica;<br />
- a continental source for most of the sediments (mostly clays)<br />
composing the radiolarites;<br />
- the existence of three depositional mechanisms for the<br />
radiolarites: 1) decantation from a turbidite system; 2) decantation<br />
of suspended material; 3) decantation from density currents<br />
(contourites). A depositional model for the lower and middle part of<br />
the Monte Facito Auct. Formation is proposed, inferring a turbiditic<br />
sedimentation.<br />
Matsuoka, A. 1989a. A key to connecting Jurassic<br />
terranes in Japan chert clastic sequence. Struct. Geol., J. Tect.<br />
Res. Groupe Japan, 34, 135-144.<br />
Matsuoka, A. 1989b. Radiolarian fossils from the<br />
Koyamada Formation (Lowest Cretaceous) of the<br />
Somanakamura Group, northeastern Japan. Fossils, 46, 11-<br />
16. (in Japanese)<br />
Radiolarian fossils have been newly discovered from the<br />
uppermost part (Koyamada Formation) of the Somanakamura Group<br />
in the eastern marginal zone of the Abukuma Mountains, northeast<br />
Japan. The <strong>radiolaria</strong>n fauna contains Pseudodictyomitra sp. cf. P.<br />
carpatica (Lozyniak), Sethocapsa sp. cf. S. kaminogoensis Aita,<br />
Hemicryptocapsa capita Tan Sin Hok, and so on. This association<br />
indicates an early Early Cretaceous age. The age assignment is<br />
consistent with that by ammonites (Berriasian).<br />
Matul', A.G. 1989a. Radiolarian distribution in the surface<br />
sediment layer in the North Atlantic. Okeanologiya, 29/6,<br />
992-998. (in Russian)<br />
Radiolarians are studied in 70 surface samples of bottom<br />
sediments in the North Atlantic from the equator to the Iceland.<br />
Distribution in sediments of 31 abundant species is studied in<br />
details. Maps for <strong>radiolaria</strong>n skeleton content in I gram of sediment<br />
and maps for distribution of 6 characteristic species are presented.<br />
An attempt to reveal interrelation between quantitative species<br />
distribution in sediments with surface water temperature is made. It<br />
is found out that every of 31 species studied has maximum of<br />
relative content at definite temperature. On this basis species<br />
temperature series in constructed, in limits of which 4 groups of<br />
<strong>radiolaria</strong>ns are distinguished in accordance with their belonging to<br />
specified temperature ranges.<br />
Matul', A.G. 1989b. The distribution of <strong>radiolaria</strong>ns in the<br />
surface layer of North Atlantic bottom sediments.<br />
Oceanology, 29/6, 740-745.<br />
The distribution of 31 species that occur in mass quantities in<br />
the sediments was studied in detail. A map of the contents of<br />
<strong>radiolaria</strong>n skeletons per 1 g of sediment and a map of the<br />
distribution of six characteristic species are presented. Each of the<br />
31 species studied has a maximum of relative contents at a<br />
particular temperature. A temperature series of the species was<br />
drawn up; within this series, four groups of <strong>radiolaria</strong>ns can be<br />
discerned by their confinement to particular temperature ranges.<br />
Menshutkin, V.V. & Petrushevska, M.G. 1989.<br />
Classification of the Collosphaeridae (Radiolaria) by<br />
Phenetical Methods. Marine Plankton: Taxonomy ecology<br />
and distibution, 41/49, 61-99. (in Russian)<br />
The 39 Neogene-Recent collosphaerid species and subspecies<br />
were investigated. Their characters and the variability were<br />
established. The main characters proved to be incongruent in the<br />
evolution. The algorithm was advanced and realised for the phenetic<br />
comparison of the taxa possesing the subjugated characters of<br />
different "weight". The best presentation of the results of that<br />
comparison appeared to be the minimal graph with the evolutionary
Radiolaria 14 Bibliography - 1989<br />
vectors. The results of the main components analysis coincided well<br />
enough to these on the mentioned graph for a half of the taxa; but<br />
the other species appeared practically undistinguished. The cladistic<br />
analysis proved to be helpless for the obtaining phylogeny of the<br />
scores of these close species with the transgressive and<br />
incongruent characters.<br />
Mizutani, S. 1989. Radiolarian fossils and the geologic<br />
history of the Japanese Islands. Observing, watching and<br />
diagnosing the basement rocks. Memorial Volume of Prof.<br />
Kojiro Nakaseko, 61-78.<br />
Mizutani, S., Shao, J.A. & Zhang, Q.L. 1989. The<br />
Nadanhada terrane in relation to Mesozoic tectonics on<br />
continental margins of East Asia. Acta geol. sinica, 3, 15-<br />
29.<br />
Morely, J.J. 1989. Radiolarian-based transfer functions<br />
for estimating paleoceanographic conditions in the South<br />
Indian Ocean. Mar. Micropaleontol., 13/4, 293-307.<br />
A quantitative analysis of 37 <strong>radiolaria</strong>n species in 58 deepsea<br />
surface-sediment samples from the subtropical to the polar<br />
regions of the Indian Ocean produced four geographically distinct<br />
faunal assemblages (transitional, antarctic, subtropical,<br />
subantarctic) . Geographic distributions of these assemblages<br />
coincide with present-day patterns of sea-surface temperature and<br />
water masses. The antarctic factor is almost exclusively found south<br />
of today's Antarctic Polar Front. Highest concentrations of the<br />
transitional factor are recorded at sites positioned between today's<br />
Subtropical Convergence and the Polar Front. The subtropical factor<br />
is dominant in sites north of today's Subtropical Convergence.<br />
Values of these four faunal assemblages in the surface-sediment<br />
samples were regressed onto present-day summer and winter<br />
temperatures of the surface waters overlying each of the core-top<br />
sites. Resulting transfer functions yield temperature estimates<br />
which compare favourably with observed (present-day) summer and<br />
winter sea-surface temperatures, with low standard errors of<br />
estimate (< ±1.9°C) and no clear geographic pattern in maps of the<br />
residuals (difference between observed and estimated sea-surface<br />
temperature).<br />
Morley, J. 1989b. Variations in high-latitude<br />
oceanographic fronts in the southern Indian Ocean; an<br />
estimation based on faunal changes. Paleoceanography, 4/5,<br />
547-554.<br />
Morley, J.J. & Heusser, L.E. 1989. Late Quaternary<br />
atmospheric and oceanographic variations in the western<br />
Pacific inferred from pollen and <strong>radiolaria</strong>n analyses.<br />
Quaternary Sci. Rev., 8, 263-276.<br />
Pollen and <strong>radiolaria</strong>n analyses of sediment from four piston<br />
cores located along a south-north transect (28-44°N) off the east<br />
coast of Japan yield detailed records of variations in terrestrial and<br />
marine climate of this region for the last 140 ka. We propose<br />
specific changes in the seasonal positions of atmospheric pressure<br />
cells to explain these climate variations that have occurred across<br />
the northeast Asian/northwest Pacific region through the most<br />
recent interglacial/glacial cycle. Results of this exercise show that<br />
there are no major discrepancies between climate reconstructions<br />
for mainland Japan inferred from pollen and those for the western<br />
Pacific derived from <strong>radiolaria</strong>ns.<br />
Mortlock, R.A. & Froelich, P.N. 1989. A simple<br />
method for the rapid determination of biogenic opal in<br />
pelagic marine sediments. Deep-Sea Res. Part A, oceanogr.<br />
Res. Pap., 36/9, 1415-1426.<br />
Nachev, I.K. & Nachev, C.I. 1989. Distribution and<br />
Evolution of Siliceous Rocks in Bulgaria. In: Siliceous<br />
Deposits of the Tethyan and Pacific Regions. (Hein, J.R. &<br />
Obradovic, J., Eds.). Springer-Verlag, New York, USA. pp.<br />
81-92.<br />
Siliceous rocks are widespread in Bulgaria and span a wide age<br />
range, from Cambrian to Quaternary. Lithologies are of different<br />
types including diatomite, spongolite, radiolarite, siliceous shale,<br />
jasper, silicified limestone, nodular chert, chert pebbles, and<br />
chalcedony sand. The mineral composition is also variable including<br />
quartz, chalcedony, cristobalite, opal-CT, and opal-A. The siliceous<br />
rocks are polygenetic. Their evolution is governed by changes in: (1)<br />
- 37 -<br />
dominance of siliceous organism types, <strong>radiolaria</strong>ns, sponges, and<br />
diatoms; (2) types of volcanic activity and tectonic environment;<br />
spreading-center basaltic volcanism, island-arc submarine basaltic<br />
volcanism, and subaerial acid volcanism; (3) sedimentary<br />
environments, openocean metachert; marginal sea siliceous shale<br />
and chert; back-arc trough siliceous shale and bedded chert;<br />
continental margin siliceous shale; intra-arc trough jasper, siliceous<br />
shale, bedded chert, nodular chert, silicified limestone, and vein<br />
agate; back-arc trough radiolarite, spongolite, and nodular chert;<br />
active continental margin silicified limestone, jasper, nodular chert,<br />
and agate; epicontinental sea nodular chert, spongolite, diatomite,<br />
and silicified limestone; Neogene lake diatomite; Quaternary<br />
fluviatile chert pebbles; Quaternary weathering chalcedony sand.<br />
Consequently, the composition and type of siliceous rocks in<br />
Bulgaria correlate well with the development of siliceous organisms,<br />
volcanic activity, and changes in the depositional and tectonic<br />
environments.<br />
Nagai, H. 1989. Supersonic vibration effect on the surface<br />
texture of Jurassic Eucyrtidiellum (Radiolaria). Bull. Nagoya<br />
Univ. Furukawa Mus., 5, 1-19. (in Japanese)<br />
The effect of supersonic vibration on the surface morphology of<br />
Jurassic Eucyrtidiellum was examined, The rock sample used in this<br />
study is a manganese carbonate nodule carrying many<br />
Eucyrtidiellum. It was taken from the southern bank of the Kiso<br />
River, Aichi Prefecture, central Japan (Nagai, 1986). Individuals of<br />
Eucyrtidiellum treated with about 10% hydrochloric acid and without<br />
supersonic vibration have always flaky materials on its surface. But<br />
we can recognize each species clearly. One minute cleaning by<br />
supersonic vibration removes almost of all of these flaky materials.<br />
A part of outer membrane of some individuals was taken away. But<br />
We can identify each species. The surface of Eucyrtidiellum, after<br />
cleaning by supersonic vibration from 5 to 15 minutes, becomes so<br />
smooth like polished metal and shows sometimes small random<br />
perforations. These perforations are quite different from pores of E.<br />
disparile.<br />
Nakaseko, K., Nishimura, A. & Yamauchi, M.<br />
1989. Paleozoic and Mesozoic <strong>radiolaria</strong>n fossils from Japan<br />
3 (Cretaceous 1-6). Atlas of Japanese fossils, 68, 1-24. (in<br />
Japanese)<br />
Nazarov, B.B. 1989. Paleozoic <strong>radiolaria</strong>ns; stratigraphic<br />
significance, evolution and relation with the development of<br />
other fauna groups. In: Problemy stratigrafii verkhnego<br />
proterozoya i fanerozoya. (Krasheninnikov, V.A., Eds.),<br />
vol. 431. Trudy - Geologicheskiy Institut (Moskva),<br />
Moscow, USSR. pp. 112-131. (in Russian)<br />
Nazarov, B.B. & Ormiston, A.R. 1989. New species<br />
of Latentifistulidae, Ruzhencevispongidae and<br />
Polyentactinidae (Polycystina, Radiolaria) from the Permian<br />
of the South Urals and Nevada. Paleont. Z., Akad. Nauk SSSR,<br />
2, 13-23.<br />
Nöthig, E.M. & Von Bodungen, B. 1989. Occurrence<br />
and vertical flux of faecal pellets of probably protozoan<br />
origin in the southeastern Weddell Sea (Antarctica). Marine<br />
Ecol. Progr. Ser., 56/3, 281-289.<br />
Amount of faecal material m the water column and in sediment<br />
traps deployed at 7 different stations was investigated during a<br />
cruise of RV "Polarstern" off Vestkapp (73°S, 19°W), Weddell Sea,<br />
Antarctica. Numerous small round, ellipsoidal or triangular pellets<br />
(30 to 150 µm) were identified in the water column and the traps.<br />
Most of the pellets contained intact, but empty, frustules of the<br />
abundant diatoms. We suggest that these small pellets were<br />
produced by protozoan grazers (ciliates, heterotrophic<br />
dinoflagellales, <strong>radiolaria</strong>ns and probably foraminifers). These<br />
pellets occurred in numbers up to 214 l -1 in the water column an(d<br />
contributed significantly (36%, of total sedimented faeces volume in<br />
traps) to vertical particle transport of empty but intact diatom<br />
frustules from the euphotic zone to deeper water layers. The<br />
greatest part of the remaining faecal material in the sediment traps<br />
consisted of larger, nearly round faecal pellets (150 to 300 µm).<br />
These faecal pellets are of unknown origin, but could have been<br />
produced by small metazoans.<br />
Obradovic, J. & Gorican, S. 1989. Siliceous deposits<br />
in Yugoslavia: occurrences, types and ages. In: Siliceous<br />
Deposits of the Tethys and Pacific Regions. (Hein, J.R. &<br />
Obradovic, J., Eds.). Springer-Verlag, New York. pp. 51-64.<br />
Siliceous deposits are widespread in Yugoslavia especially in<br />
Mesozoic sections. They first occur in Middle Triassic deposits and
Bibliography - 1989 Radiolaria 14<br />
continue through Jurassic and Cretaceous sections. All of these<br />
Mesozoic siliceous deposits are of marine origin. Generally three<br />
lithologic associations with chert are recognized in the Mesozoic<br />
sections. 1. the Porphyrite-chert assemblage of Middle-Late Triassic<br />
age, 2. the Diabase-chert Formation of Middle-Late Jurassic age, and<br />
3. carbonate complexes of Middle Triassic to Danian ages. The first<br />
two lithologic associations are connected with the breakup of the<br />
Dinaridic plate at the end of Early Triassic, which was followed by<br />
hybrid volcanic activity with the greatest production of volcanic<br />
rocks in the Ladinian. At that time an oceanic region developed, and<br />
existed to the Late Jurassic. Bedded chert formed on transitional and<br />
oceanic crust. They formed in different parts of this oceanic basin<br />
by different depositional mechanisms. Commonly, olistoliths of the<br />
porphyrite-chert assemblage occur in the Diabase-chert Formation.<br />
Siliceous deposits associated with carbonate complexes occur in<br />
different parts of Yugoslavia, but as an example of this lithologic<br />
association we discuss the occurrences in the Budva zone,<br />
Montenegin Littoral. The Budva zone represents a depositional<br />
trough on thinned continental crust situated between two carbonate<br />
platforms. The sedimentation of carbonate rocks with bedded chert<br />
took place mostly on the slopes, beginning with subtidal deposition in<br />
the latest Ladinian and evolving later into open-shelf deposition.<br />
O'Dogherty, L. 1989. Bioestratigrafía y Paleontología de<br />
las Facies con Radiolarios del Jurásico medio- superior de la<br />
Cordillera Bética. Tesis de Licenciatura. Universidad de<br />
Granada, 1-119 p. (unpublished)<br />
O'Dogherty, L., Aguado, R., Sandoval, J. &<br />
Martínez-Gallego, J. 1989b. Datos bioestratigráficos de<br />
las facies radiolaríticas del Jurásico Subbético. Cuad. Geol.<br />
ibérica, 13, 53-65.<br />
Radiolarian-rich siliceous facies of the Middle and Upper<br />
Jurassic were studied in four stratigraphic sequences located in<br />
different areas of the Middle Subbetic Zone. Two stratigraphic units<br />
are recognized. Calcareous radiolarites of the middle-upper<br />
Callovian and siliceous mudstones and marls of the uppermost<br />
Callovian to Oxfordian. The <strong>radiolaria</strong>n assemblages recovered from<br />
the four sections permit to recognize the <strong>radiolaria</strong>n zones A0, Al,<br />
A2, B, C1 and C2 of Baumgartner (1987) in the upper Bajocian to<br />
lower Tithonian. Ammonite faunas recovered from interbedded<br />
calcareous layers allow for more precise ties of the <strong>radiolaria</strong>n<br />
zones to the stages.<br />
O'Dogherty, L., Sandoval, J., Martin-Algarra, A.<br />
& Baumgartner, P.O. 1989a. Las facies con radiolarios<br />
del Jurásico subbético (Cordillera Bética, Sur de España). Rev.<br />
Soc. mex. Paleont., 2, 70-77.<br />
In this paper we establish the biostratigraphy by means of<br />
Radiolaria and calcareous nannoplankton of the siliceous materials<br />
from three stratigraphic sequences located in different Middle<br />
Subbetic areas. The above cited series contain ammonite fauna in<br />
the under and/or overlying levels to the siliceous materials, and<br />
therefore the datations are simplified. For the interval uppermost<br />
Bajocian-lowermost Kimmeridgian we can recognize the <strong>radiolaria</strong>n<br />
zones Al, A2, B and C1, which has been established by Baumgartner<br />
(1987) in the Western Tethys. Calcareous nannoplankton permits to<br />
distinguish two different intervals: a lower, Bajocian to Lower<br />
Callovian age and other one Callovian to Oxfordian.<br />
Okada, H., Tarduno, J.A., Nakaseko, K.,<br />
Nishimura, A., Sliter, W.V. & Okada, H. 1989.<br />
Microfossil assemblage from the Late Jurassic to Early<br />
Cretaceous Nikoro Pelagic Sediments, Tokoro Belt,<br />
Hokkaido, Japan. Mem. Fac. Sci., Kyushu Univ., Series D<br />
(Earth planet. Sci.), 27/3, 193-214.<br />
The Tokoro Belt in Hokkaido constitutes one of the major<br />
ophiolitic belts in the Japanese Islands. In order to clarify the origin<br />
of the Tokoro ophiolitic rocks which are represented by the Nikoro<br />
Group, new micropaleontologic data of the Nikoro pelagic sediments<br />
are presented in this paper as regards <strong>radiolaria</strong>ns, calcareous<br />
nannofossils and foraminifers. The results show that (1) the age of<br />
the Nikoro Group ranges from the Kimmeridgian to the early Albian,<br />
and (2) the Nikoro pelagic rocks were deposited in a seamount<br />
environment near an oceanic ridge in the paleoequatorial productive<br />
region, where the paleodepth was about 1000 m and above the CCD.<br />
Pessagno, E.A., Six, W.M. & Yang, Q. 1989. The<br />
Xiphostylidae Haeckel and Parvivaccidae, n. fam.,<br />
(Radiolaria) from the North American Jurassic.<br />
Micropaleontology, 35/3, 193-255.<br />
This report deals with the Parvivaccidae, n. fam. and a revision<br />
of the Xiphostylidae Haeckel. Both of these spumellarian families are<br />
- 38 -<br />
unique in that they possess cortical shells consisting of two distinct<br />
fused layers of latticed meshwork. Three new genera and twentynine<br />
new species are described from the Xiphostylidae Haeckel.<br />
Emended definitions are presented for Triactoma Ruest, Tripocyclia<br />
Haeckel, and Xiphostylus Haeckel. Two new genera and two new<br />
species are described under the Parvivaccidae. Only Jurassic<br />
xiphostylid and parvivaccid taxa are figured herein. Range,<br />
occurrence, and relative abundance of the more important taxa are<br />
shown in the text-figures.<br />
Popova, I.M. 1989. Radiolarians from Neogene sediments<br />
section of South Sakhalin (between the rivers Kura-Uryum).<br />
In: Cenozoic of the Far East. (Krasilov, V.A. & Klimora,<br />
R.S., Eds.). Akademiya Nauk SSSR, Dalnevostochnoe<br />
otdelenie Biologo-Pochvennyi Institut, Vladivostok, USSR.<br />
pp. 209-217. (in Russian)<br />
Prell, W., Niitsuma, N., Emeis, K. et al. 1989.<br />
Tectonique et sédimentation néogene sur la marge d'Oman.<br />
Résultats préliminaires du Leg 117 ODP. C.R. Acad. Sci.<br />
(Paris), Sér. II, 308, 663-669.<br />
Reimers, C.E. & Wakefield, W.W. 1989.<br />
Flocculation of siliceous detritus on the sea floor of a deep<br />
Pacific seamount. Deep-Sea Res. Part A, oceanogr. Res. Pap.,<br />
36/12, 1841-1861.<br />
A benthic layer of flocculated material, which was centimetres<br />
thick in and around biogenic sediment structures on the carbonatecovered<br />
cap of Magellan Rise (7° N, 177° W; equatorial Pacific),<br />
consisted of a meshwork of delicate and spiny forms of <strong>radiolaria</strong>ns<br />
including phaeodarians. Like phytodetritus, patches of degraded floc<br />
appear to be disrupted on relatively short time scales by surface<br />
deposit-feeding megafauna. This destruction is through ingestion of<br />
surface sediment particles and erasure of sediment structures<br />
serving as benthic particle maps.<br />
Rio, D., Thunell, R., Sprovieri, R., Bukry, D.,<br />
Destefano, E., Howell, M., Raffi, I., Sancetta,<br />
C. & Sanfilippo, A. 1989. Stratigraphy and depositional<br />
history of the Pliocene Bianco section, Calabria, southern<br />
Italy. Palaeogeogr. Palaeoclimatol. Palaeoecol., 76/1-2, 85-<br />
105.<br />
An integrated micropaleontological and geochemical study was<br />
carried out on the Pliocene-age Bianco section located in Calabria,<br />
southern Italy. This section is somewhat unique for the Pliocene of<br />
the Mediterranean region in that it contains abundant calcareous and<br />
siliceous microfossils. Based on the biostratigraphic findings, it<br />
ranges in age from approximately 3.7-3.0 Ma. The Bianco section is<br />
composed of marly mudstones intercalated with diatomites, with the<br />
diatomites being particularly common in the upper 50 m of the<br />
section (above 3.1 Ma).<br />
The diatomites contain an abundant benthic foraminiferal<br />
assemblage and have a low organic carbon content indicating that<br />
bottom waters were fairly well-oxygenated during their deposition.<br />
Faunal and floral indicators suggest a cooling of surface waters in<br />
this region at 3.1 Ma. The diatom assemblages within the Bianco<br />
diatomites are very similar to those living in the Gulf of California,<br />
suggesting an upwelling origin for these silica-rich units. A model is<br />
proposed which attributes diatomite formation to upwelling induced<br />
by climatically controlled changes in local hydrography.<br />
Roonwal, G.S. & Vijaya-Kumar, U. 1989. In-situ<br />
growth of authigenic minerals and micronodules in some<br />
pelagic sediments from the Central Pacific. J. geol. Soc.<br />
India, 34/6, 647-650.<br />
Zeolite crystals dcveloped in-situ arc noted in the siliceous<br />
ooze in the north equatorial Pacific. Micronodules with well<br />
developed initial growth lines, formed authigenically are commonly<br />
observed in the siliceous debris-rich calcareous ooze of south<br />
equatorial Pacific. Quartz and feldspars of detrital origin are also<br />
found in the sediment.<br />
Ruiz-Ortiz, P.A., Bustillo, M.A. & Molina, J.M.<br />
1989. Radiolarite sequences of the Subbetic, Betic Cordillera,<br />
southern Spain. In: Siliceous Deposits of the Tethys and<br />
Pacific Regions. (Hein, J.R. & Obradovic, J., Eds.). Springer-<br />
Verlag, New York. pp. 107-127.<br />
The radiolarite sequence of the middle Subbetic (Betic<br />
cordillera, southern Spain) is composed of three main lithologies:<br />
radiolarite, siliceous mudstone and marl, and pelagic limestone with<br />
<strong>radiolaria</strong>ns. Virtually all transitional lithologies among the three
Radiolaria 14 Bibliography - 1989<br />
listed exist. Clay minerals, calcite, and hematite make up the<br />
radiolarite impurities. Smectite, illite, and locally kaolinite are the<br />
clay minerals present, smectite always being most abundant. No<br />
radiolarite bed with more than 85% silica has been found; the total<br />
SiO2 content ranges from 61 to 85% . Frequently the compact<br />
appearance of the radiolarite results from a high carbonate content.<br />
The ratios Si/Si + Al + Fe + Ca, Si/Si + Al + Fe, and Al/Al + Fe + Mn<br />
are calculated and used to compare the beds of couplets in rhythmic<br />
sequences and to obtain the relative distance of sections from their<br />
terrigenous source. These three chemical indices do not give<br />
consistent results. Fe enrichment of radiolarite relative to siliceous<br />
mudstone is probably related to the }ow mean sedimentation rate of<br />
these sequences from the Subbetic (3.5 mm/l000 y). Pelagic<br />
settling in a basin with irregular bottom topography and with areas<br />
topographically protected from sediment input is proposed for<br />
deposition of these deposits. Productivity cycles and terrigenous<br />
dilution gave rise locally to rhythmically bedded sequences, usually<br />
composed of radiolarite-mudstone alternations. Locally, contour and<br />
distal dilute turbidity currents reworked and deposited the sediment,<br />
and gave rise to thin sequences of layered sedimentary rocks and to<br />
laminated beds. Deposition above a relatively shallow CCD is<br />
deduced, and a water depth shallower than previously thought is<br />
suggested for these deposits, which are considered as the deepest<br />
water deposits of the Betic External Zones.<br />
Saito, M. 1989. Jurassic melanges in the Taniguni area,<br />
Gifu Prefecture, Mino terrane. J. geol. Soc. Japan, 95/8, 579-<br />
594. (in Japanese)<br />
Jurassic melanges in the Tanigumi area of the Mino terrane<br />
consist of three units, i.e. melange I, II and m Melange I includes<br />
exclusively sandstone-blocks whereas melange II is characterized by<br />
chert-, shale-, and sandstone-blocks and melange III is by<br />
greenstone-limestone-, dolostone-, chert-, shale- and sandstone<br />
blocks. Biostratigraphic data examined for blocks and matrix in the<br />
southern part of the study area show that the original lithologic<br />
succession of melange II includes the following formations, in<br />
ascending order- middle Permian chert, middle Triassic to late early<br />
Jurassic chert, early middle Jurassic shale, and late middle Jurassic<br />
mudstone and sandstone(?).<br />
Sashida, K., Igo, H., Adachi, S. & Ito, S. 1989.<br />
Radiolarian dating of the Torinosu-type limestone in the<br />
Kanto Mountains, Central Japan. Annu. Rep. Inst. Geosci.,<br />
Univ. Tsukuba, 15, 54-60.<br />
The "Torinosu Limestone" crops out typically a Torinosu,<br />
Sakawa Town, Kochi Prefecture, Shikoku This limestone is an<br />
important constituent of the Torinosu Group, which is one of the<br />
most classical standard lithostratigraphic units of the Upper<br />
Jurassic in Japan. It is mostly black and bituminous and yields<br />
abundant fossils of reef dwellers such as corals, stromatoporoids,<br />
algae, molluscs, brachiopods, echinoids, foraminifers and others. The<br />
geologic age of this limestone has long been thought to be Late<br />
Jurassic based mainly on hexacorals and stromatoporoids. Similar<br />
limestones are known elsewhere in the Outer Zone of the Japanese<br />
Islands and have been called collectively "Torinosu Limestone" or<br />
Torinosu type limestone. Recent studies on the age of the Torinosu<br />
Group and its equivalent of Southwest Japan using <strong>radiolaria</strong>n<br />
biostratigraphy clearly showed that it ranges from Middle Jurassic to<br />
Early Cretaceous (e.g., Matsuoka and Yao, 1985; Suyari and Ishida,<br />
1985; Yasuda, 1989). Aita and Okada (1986), Aita (1987) and<br />
Ishida (1988) also clarified the age of the Torinosu type limestone<br />
using nannofossils in Shikoku. These microfossils indicate early Late<br />
Jurassic to earliest Cretaceous ages. We have been engaged in the<br />
study to confirm detailed dating of the Torinosu-type limestone in<br />
the Kanto Mountains. To date, we found <strong>radiolaria</strong>ns in the Torinosu<br />
type limestone embedded in the Hikawa and Gozenyama Formations<br />
of the Southern Chichibu Terrane and in the Oonari and Kosode<br />
Formations of the Ogouchi Group of the Northern Shimanto Terrane.<br />
Foraminifers were also extracted together with a small amount of<br />
<strong>radiolaria</strong>ns from the Torinosu-type limestone interbedded in the<br />
Ishido Formation of the Sanchu Cretaceous formations (Fig. 1). We<br />
briefly describe herein these <strong>radiolaria</strong>ns extracted by the<br />
hydrochloric acid method and discussed their dating.<br />
Sato, T., Sashida, K. & Kasai, K. 1989. Mesozoic<br />
system in the Yamizo Mountains. Excursion Guide Book,<br />
96th Annual Meeting of the Geological Society of Japan, 31-<br />
54.<br />
Sharma, V. & Sharma, G.K. 1989. Late Miocene to<br />
early Pliocene <strong>radiolaria</strong>n biostratigraphy of Neill Island,<br />
Andaman Sea. J. geol. Soc. India, 34, 76-82.<br />
104 species of Radiolaria are recorded from a Late Miocene-<br />
Early Pliocene sequence exposed at Neill Island. The assemblage<br />
shows presence of a few reworked <strong>radiolaria</strong>n species. The<br />
<strong>radiolaria</strong>n zones proposed for low latitude areas are applicable in<br />
- 39 -<br />
the present study. Two zones, viz.., Didymocyrtis penultima Zone and<br />
Stichocorys peregrina Zone, have been recognized in the sequence.<br />
Based on the study of planktonic Foraminifera of the same sequence<br />
by earlier workers, an integrated scheme of <strong>radiolaria</strong>n and<br />
foraminiferal zones is presented.<br />
Shemesh, A., Mortlock, R.A. & Froelich, P.N.<br />
1989. Late Cenozoic Ge/Si record of marine biogenic opal:<br />
implications for variations of riverine fluxes to the ocean.<br />
Paleoceanography, 4/3, 221-234.<br />
We have determined germanium/silicon ratios in purified<br />
diatoms and <strong>radiolaria</strong>ns from siliceous sediments in Holocene core<br />
tops, one late Pleistocene piston core, and four high-latitude DSDP<br />
sites ranging in age from Holocene to Oligocene. Low values of the<br />
ratio are consistent with global weathering regimes dominated by<br />
river silica input to the sea, while higher ratios suggest periods of<br />
enhanced hydrothermal input or reduced fluvial contribution.<br />
Shu, D. & Chen, L. 1989. Discovery of Early Cambrian<br />
Radiolaria and its significance. Sci. China, Ser. B, 32/8,<br />
986-994.<br />
The well-preserved bivalved microfossils collected from the<br />
Lower Cambrian limestone at the Xiaoyang section in Zhenba,<br />
Shaanxi, have proved the oldest known <strong>radiolaria</strong>ns by means of the<br />
electron probing analysis and morphological study under the electron<br />
scanning microscope and the observation of the thin section. The<br />
present discovery has shaken the theory that Thaeodaria originated<br />
from Spumellaria. Unlike the Mesozoic and Cenozoic <strong>radiolaria</strong>ns<br />
that are planktonic, the Cambrian ones lived as benthos. On the<br />
basis of the chemical composition and morphological features of<br />
these <strong>radiolaria</strong>ns a new genus Eoconcharium and a new family<br />
Eoconchariidae are erected.<br />
Spörli, K.B., Aita, Y. & Gibson, G.W. 1989.<br />
Juxtaposition of Tethyan and non-Tethyan Mesozoic<br />
<strong>radiolaria</strong>n faunas in melanges, Waipapa Terrane, North<br />
Island, New Zealand. Geology, 17/8, 753-756.<br />
Red cherts from Kawakawa Bay near Auckland have yielded Late<br />
Triassic and Early Jurassic <strong>radiolaria</strong>ns. The cherts occur as blocks<br />
in melanges that have a green argillite matrix containing Middle and<br />
Late Jurassic (Callovian-Oxfordian) <strong>radiolaria</strong>ns. The melanges mark<br />
fault zones along which the Waipapa terrane has been imbricated.<br />
Callovian-Oxfordian green argillites are also found in stratigraphic<br />
contact with overlying Kimmeridgian-Tithonian green argillites and<br />
gray terrigenous clastics. The Late Triassic and Early Jurassic<br />
Radiolaria are Tethyan, but me Middle and Late Jurassic faunas are<br />
dominantly non-Tethyan because the two sets of faunas are of lowlaatude<br />
and of high-latitude origin, respectively, or because they<br />
originated in areas of differing ocean productivity. Occurrence of<br />
both Late Triassic and Early Jurassic <strong>radiolaria</strong>ns in one red chert<br />
horizon indicates sedimentary reworking.<br />
Stamatakis, M., Dermitzakis, M., Economou-<br />
Amilli, A. & Magganas, A. 1989. Petrology and<br />
Diagenetic Changes in Miocene Marine Diatomaceous<br />
Deposits from Zakynthos Island, Greece. In: Siliceous<br />
Deposits of the Tethys and Pacific Regions. (Hein, J.R. &<br />
Obradovic, J., Eds.). Springer-Verlag, New York. pp. 129-<br />
140.<br />
Stamatakis, M. & Magganas, A. 1989. Thermally<br />
Induced Silica Transformation in Pliocene Diatomaceous<br />
Layers from Aegina Island, Greece. In: Siliceous Deposits of<br />
the Tethys and Pacific Regions. (Hein, J.R. & Obradovic, J.,<br />
Eds.). Springer-Verlag, New York. pp. 141-150.<br />
Suyari, K., Kuwano, Y. & Yamasaki, T. 1989.<br />
Distribution of lithofacies and geological ages in the<br />
Shimanto South Subbelt in Eastern Shikoku. J. Sci., Univ.<br />
Tokushima, 22, 33-57. (in Japanese)<br />
Takahashi, O., Hayashi, N. & Ishii, A. 1989.<br />
Radiolarian fossils from the Masutomi Group, southwestern<br />
part of the Kanto Mountains, central Japan, and their<br />
significance. J. geol. Soc. Japan, 95/12, 953-955. (in<br />
Japanese)<br />
Takahashi, O., Imai, H. & Ishii, A. 1989.<br />
Occurrence of Cretaceous <strong>radiolaria</strong>ns from the Otaki Group,<br />
Kanto Mountains, central Japan. J. geol. Soc. Japan, 95/6,<br />
483-486. (in Japanese)
Bibliography - 1989 Radiolaria 14<br />
Tan, Z.Y. & Su, X.H. 1989. Studies on the Acantharian<br />
cysts of the south china Sea. Stu. marina sinica, 30, 139.<br />
In May, 1958 and February 1961, we carried out investigations<br />
from off shore waters of southeast Hainan Island between latitudes<br />
16°—22° N, longitudes 110°—115° E. with the purpose of collecting<br />
acantharian specimens. All the samples from forty seven stations of<br />
this area were examined. Forty acantharian cysts of different<br />
shapes had been found from six stations (fig. 1). According to our<br />
observation and previously published information, from the<br />
morphological point of view, there seems to be three phases during<br />
the process of cyst formation: Prophase - The central structure of<br />
spines in cyst is not separated yet. Metaphase - The central<br />
structure of spines in cyst is already separated but more or less still<br />
retaining some structure characteristic of spines. Anaphase- The<br />
spines in the cyst have all disappeared. According to their shape and<br />
the structural characteristics of spines, these cysts may be divided<br />
into two groups:<br />
Group I Includes all the cyst in the prophase stage and a few<br />
cysts in the metaphase stage. They could be identified to genus but<br />
not to species. It includes 10 formas under five genera 1. Genus<br />
Acanthocyrta (1) Forma Allas (2) Forma Folium (3) Forma Pepo (4)<br />
Forma Fusus 2. Genus Acanthocolla (5) Forma Bimamma (6) Forma<br />
Chrysallis (7) Forma Oliva 3. Genus Acantholithium (8) Forma<br />
Ampulla 4. Genus Haliommatidium (9) Forma Strobila 5. Genus<br />
Conacon (10) Forma Strophinx<br />
Group II Includes some cysts in the metaphase stage and all<br />
cysts in the anaphase stage. It includes 9 formas which could not be<br />
allocated to any genus<br />
Tanaka, H. 1989. Mesozoic formations and their<br />
molluscan faunas in the Haidateyama area, Oita prefecture,<br />
southwest Japan. J. Sci. Hiroshima Univ., Ser. C: Geol.<br />
Min., 9/1, 1-45.<br />
Tumanda, F. 1989. Cretaceous <strong>radiolaria</strong>n biostratigraphy<br />
in the Eashi Mountain area, Northern Hokkaido, Japan. Sci.<br />
Rep. Inst. Geosci., Univ. Tsukuba, Sect. B: geol. Sci., 10, 1-<br />
44.<br />
The stratigraphy of the Esashi Mountain area was restudied in<br />
view of establishing the Cretaceous <strong>radiolaria</strong>n biostratigraphy. The<br />
age assignments of the different formations were re-evaluated and<br />
confirmed mainly by Radiolaria, supplemented by Foraminifera, and<br />
inoceramid bivalves. Four <strong>radiolaria</strong>n assemblage zones are<br />
proposed herein. These are the Staurosphaera septemporata—<br />
Parvicingula usotanensis, Archaeodictyomitra simplex, Thanarla<br />
praeveneta—Holocryptocanium geysersense, and Alievium<br />
praegallowayi—Amphipyndax sp. A Assemblage Zones in ascending<br />
order. Correlation of the proposed zones with those of other authors<br />
is discussed.<br />
A total of 188 <strong>radiolaria</strong>n species were identified, figured<br />
herein and listed in tables with their geographic and stratigraphic<br />
distribution and relative abundance. Among the <strong>radiolaria</strong>n species,<br />
11 new species and 2 new subspecies are systematically described.<br />
Van Bennekom, A.J., Jansen, J.H.F., Van der<br />
Gaast, S.J., M., V.I. & Pieters, J. 1989. Aluminiumrich<br />
opal: an intermediate in the preservation of biogenic<br />
silica in the Zaire (Congo) deep-sea fan. Deep-Sea Res. Part<br />
A, oceanogr. Res. Pap., 36/2, 173-190.<br />
Diatom frustules, skeletons of <strong>radiolaria</strong>ns and<br />
silicoflagellates, and also phytoliths in the sediments of the Zaire<br />
deep-sea fan have a crumbly appearance, very spongy<br />
ultrastructures and have very high atomic Al/Si ratios between 0.13<br />
in the inner parts and 0.16 in the outer parts of the fan. Also small<br />
amounts of Ca and K are always found. The high Al content is related<br />
to a shift of the amorphous Silica bulge in XRD spectra from 0.41 to<br />
0.36-0.37 nm, which shows that Al has substituted Si throughout<br />
the entire test of the great majority of the siliceous microfossils.<br />
This substitution is related to a low apparent solubility of about 350<br />
mmol m -3 of H 4 SiO 4 , and to a low Silica release-rate constant of 1-2<br />
x 10 -12 cm s -1 . The high content of Al in biogenic Silica is caused by<br />
a combination of selective dissolution of Silica and precipitation of<br />
Al dissolved from minerals in the sediment. The Zaire deep-sea fan<br />
combines several environmental factors favourable for the<br />
formation of Al-rich opal, viz. a large production of diatoms in<br />
offshore waters, a high concentration of dissolved Al in plume<br />
waters, and the presence of kaolinite and gibbsite (both minerals<br />
which easily release Al) in the sediment supplied by the Zaire River.<br />
Van de Paverd, P.J. & Bjørklund, K.R. 1989.<br />
Frequency distribution of polycystine <strong>radiolaria</strong>ns in surface<br />
sediments of the Banda Sea, eastern Indonesia. Netherl. J. Sea<br />
Res., 24/4, 511-512.<br />
- 40 -<br />
Numbers of <strong>radiolaria</strong>ns per gram carbonate-free seafloor<br />
sediment vary widely in the Banda Sea. They are low from 0 to 950<br />
m, high between 950 and 4800 m, and ('abnormally') low again<br />
below 4800 m water depth. We conclude that this distribution<br />
pattern is the result of masking by sediment and the occurrence of<br />
spatially limited highly productive areas in the surface water.<br />
Vecsei, A., Frisch, W., Pirzer, M. & Wetzel, A.<br />
1989. Origin and tectonic significance of <strong>radiolaria</strong>n chert in<br />
the Austroalpine rifted continental margin. In: Siliceous<br />
Deposits of the Tethys and Pacific Regions. (Hein, J.R. &<br />
Obradovic, J., Eds.). Springer-Verlag, New York. pp. 65-80.<br />
Rhythmically bedded <strong>radiolaria</strong>n chert of Late Jurassic age<br />
(Ruhpolding Formation) was deposited by bottom currents and lowdensity<br />
turbidity currents in the Northern Calcareous Alps. The<br />
<strong>radiolaria</strong>ns were concentrated by sorting of hydrodynamically<br />
equivalent particles. High production of <strong>radiolaria</strong>ns and low<br />
terrigenous input were characteristic of these deposits. Carbonate<br />
dissolution was of secondary importance. The <strong>radiolaria</strong>n chert was<br />
deposited below the aragonite compensation depth, but for the most<br />
part, above the calcite compensation depth.<br />
Deposition of the <strong>radiolaria</strong>n chert marks a change in the<br />
tectonic and topographic setting of the Austroalpine rifted<br />
continental margin. A horst and graben pattern, formed at the<br />
beginning of the Jurassic, was replaced at the time of the<br />
Oxfordian/Kimmeridgian boundary by a tilted block array facing the<br />
Piemont Ocean. The change in topography enabled an open, lowenergy<br />
current system to be established, which was responsible for<br />
the deposition of the <strong>radiolaria</strong>n chert. Steepening of the topography<br />
resulted in sedimentation by high-energy bottom currents and<br />
various types of sediment gravity flows along the steep flanks of the<br />
asymmetrical tiltblock basins (Tauglboden Formation).<br />
Vishnevskaya, V.S., Agarkov, Y.V., Zakariadze,<br />
G.S. & Sedaeva, K.M. 1989. Upper Jurassic-Cretaceous<br />
<strong>radiolaria</strong>ns from the High-Caucasus a tool to correlate the<br />
development and the genetic conditions of the ophiolites in<br />
the Low-Caucasus. Dokl. Akad. Nauk SSSR, 310/6, 1417-<br />
1421. (in Russian)<br />
Vitukhin, D.I. 1989. Neogene <strong>radiolaria</strong>n complexes from<br />
Kuril Islands sediments (Kunashir, Iturup). In: Cenozoic of<br />
the Far East. (Krasilov, V.A. & Klimora, R.S., Eds.).<br />
Akademiya Nauk SSSR, Dalnevostochnoe otdelenie Biologo-<br />
Pochvennyi Institut, Vladivostok, USSR. pp. 206-208. (in<br />
Russian)<br />
Watanabe, Y., Iwata, K. & Hasaka, T. 1989.<br />
Stratigraphy and structure of the Miocene in the Jozankei<br />
area, southwestern Hokkaido. Earth Sci., J. Assoc. geol.<br />
Collab. Japan, 43/1, 7-15. (in Japanese)<br />
Willmann, R. 1989. Evolutionary or biological species?<br />
Abh. naturwiss. Ver. Hamburg, NF, 28, 95-110.<br />
Yamagata, T. 1989. Mesozoic chaotic formations of Mino<br />
Terrane, northwestern Mino Mountains, central Japan. J.<br />
geol. Soc. Japan, 95/6, 447-461.<br />
The paper describes tectonostratigraphy, lithologic features,<br />
and ages by <strong>radiolaria</strong>ns of Mesozoic formations of the Mino terrane<br />
in the northwestern Mino Mountains, central Japan. The Mesozoic<br />
formations are divided into the Neo, Taniai, and Kuzuhara<br />
Pormations, forming a north-dipping thrust nappe complex. Two<br />
modes of occurrence of exotic rock-bodies are confirmed in the<br />
chaotic formations. One is laterally continuous large-scale, thrustbounded<br />
slabs of chert and siliceous shale or ones of sandstone and<br />
alternating beds of sandstone and shale. The other is laterally<br />
discrete, isolated, various-sized pods of chert, siliceous shale, and<br />
basaltic rocks, all of which are disorderly enclosed in the scaly<br />
cleaved mudstone. Dating of the mudstone as matrix by <strong>radiolaria</strong>n<br />
fossils shows that the Neo Formation is referable to the upper<br />
Middle to uppermost Upper Jurassic and the Tanial Formation is<br />
referred to the middle to uppermost Upper Jurassic. The age of the<br />
mudstone of each formation is younging to the south.<br />
Yamato-Omine-Research-Group 1989. Paleozoic and<br />
Mesozoic systems in the central area of the Kii mountains,<br />
southwest Japan (Part 3). Mesozoic of the Miyoshino district<br />
in Nara Prefecture. Earth Sci., J. Assoc. geol. Collab. Japan,<br />
43/3, 119-128. (in Japanese)
Radiolaria 14 Bibliography - 1989<br />
Yamauchi, M. 1989. Radiolarian assemblage in JT-01<br />
sediment trap sample. Kaiyo Monthly, 21/4, 203-208.<br />
Yang, Q. & Pessagno, E.A. 1989. Upper Tithonian<br />
Vallupinae (Radiolaria) from the Taman Formation, eastcentral<br />
Mexico. Micropaleontology, 32/2, 114-134.<br />
The pantanelliid subfamily Vallupinae Pessagno and MacLeod<br />
reached its acme of development during the late Tithonian. Two new<br />
genera (Neovallupus and Supervallupus) and seven new species are<br />
described from the upper Tithonian portion of the Taman Formation,<br />
east-central Mexico; new species are Bivallupus oppositus, B.<br />
primigenus, Neovallupus dumitricai, N. modestus, Protovallupus<br />
excellens, Supervallupus haeckeli, and Vallupus laxus. In addition,<br />
the definition of the subfamily Vallupinae is emended. Many taxa<br />
belonging to the Vallupinae are short-ranging, distinctive, and<br />
cosmopolitan—occurring in both Boreal and Tethyan strata.<br />
Vallupinid taxa have proven to be useful in developing a meaningful<br />
<strong>radiolaria</strong>n zonation for the upper Tithonian of North America.<br />
Yao, A. 1989. Paleozoic and Mesozoic <strong>radiolaria</strong>n fossils<br />
from Japan (Triassic 1-3). Atlas of Japanese fossils, 66, 1-<br />
12. (in Japanese)<br />
Yasuda, M. 1989. Equivalents to the Torinosu Group of the<br />
Chichibu Belt in the southeastern part of the Kanto<br />
Mountans, central Japan; lithology and <strong>radiolaria</strong>n<br />
biostratigraphy. J. geol. Soc. Japan, 95/6, 463-478. (in<br />
Japanese)<br />
Mesozoic sedimentary complexes of middle and southern<br />
Chichibu Belt in the southeastern part of the Kanto Mountains are<br />
composed of three types of strata, namely, (1) chert-clastics<br />
strata, (2) chaotic strata and (3) clastics with limestone strata (the<br />
equivalent to the Torinosu Group). In this paper, the strata of type<br />
(3) in the area is described, and further the age by <strong>radiolaria</strong>n<br />
remains and its geological significance are discussed.<br />
The equivalents of the Torinosu Group in the area are the<br />
Itsukaichi Formation (lower-upper Middle Jurassic), the Kowada<br />
Formation (lower Upper-Jurassic) and the Hikawa Formation (middle<br />
Upper Jurassic-Lower Cretaceous: Akaisawa area; Lower<br />
Cretaceous: Hinatagayato area; lower-upper Upper Jurassic).<br />
Commonly, these formations consist mainly of terrigenous<br />
clastics mudstone, sandstone, alternation of sandstone and<br />
mudstone, rarely conglomerate) and limestone (Torinosu-type) not<br />
including other allochthonous or older blocks. The Itsukaichi and<br />
Hikawa (Akaisawa area) Formations show stratigraphic change of<br />
<strong>radiolaria</strong>n assemblage. So these strata are regarded as normally<br />
accumulated sediments of clastics, having little processes of mixing<br />
and reconstruction. Judging from the relative position of<br />
contemporaneous heterotopic facies formations, depositional site of<br />
these strata was situated at the northeastern side of those of chertclastics<br />
and chaotic strata.<br />
Abelmann, A. 1990. Oligocene to Middle Miocene<br />
<strong>radiolaria</strong>n stratigraphy of southern high latitudes from Leg<br />
113, sites 689, and 690, Maud Rise. In: Proceedings of the<br />
Ocean Drilling Program, Scientific Results. (Baker, P.F.,<br />
Kennett, J.P. et al., Eds.), vol. 113. College Station, TX<br />
(Ocean Drilling Program), pp. 675-708.<br />
At Sites 689 and 690, drilled during ODP (Ocean Drilling<br />
Program) Leg 113 on the Maud Rise (southeast Weddell Sea),<br />
moderately to well preserved <strong>radiolaria</strong>n assemblages were obtained<br />
from continuously recovered upper Oligocene and Neogene<br />
sequences. Based on <strong>radiolaria</strong>n investigations, a biostratigraphic<br />
zonation for a time interval covering the late Oligocene to the middle<br />
Miocene is proposed. The <strong>radiolaria</strong>n zonation comprises 10 zones.<br />
Five zones are new, and five zones previously defined by Chen<br />
(1975) were modified. The zones and the ranges of the nominate<br />
species are directly calibrated with a geomagnetic polarity record.<br />
This is the first attempt at a direct correlation of late Oligocene to<br />
middle Miocene <strong>radiolaria</strong>n zones with the geomagnetic time scale.<br />
Six hiatuses were delineated in the studied upper Oligocene to middle<br />
Miocene sections. One major hiatus, spanning ca. 6 m.y., is between<br />
the upper Oligocene and the lower Miocene sequences. Another<br />
important hiatus separates the lower and middle Miocene sediments.<br />
As a base for the biostratigraphic investigations, a detailed<br />
taxonomic study of the recovered <strong>radiolaria</strong>n taxa is achieved. Three<br />
new <strong>radiolaria</strong>n species that occur in upper Oligocene and lower<br />
Miocene sediments are described (Cycladophora antiqua,<br />
Cyrtocapsella robusta, and Velicucullus altus).<br />
1990<br />
- 41 -<br />
Yeh, K.Y. 1989. Studies of Radiolaria from Fields Creek<br />
Formation, east-central Oregon, U.S.A. Bull. natl. Mus. nat.<br />
Sci., Taiwan, 1, 43-109.<br />
From the Fields Creek Formation, east-central Oregon, four<br />
major <strong>radiolaria</strong>n assemblages were recovered, they are the Ladinian<br />
Pseudostylosphaera magnispinosa Assemblage, Karnian Poulpus<br />
karnicus Assemblage, Norian Corum parvum Assemblage, and an<br />
upper Norian or Hettangian fauna of Orbiculiform sp. A Assemblage.<br />
Characteristic species of each assemblage and other distinct<br />
<strong>radiolaria</strong>n taxa including twenty three new species and four new<br />
genera are figured and described in this report. The results of this<br />
study indicate that (1) the Fields Creek Formation was mainly<br />
deposited during Norian times, but the deposition of the Fields Creek<br />
sediment may have initiated from Ladinian times, or (2) the rocks<br />
contain Ladinian or Karnian Radiolaria represent the allochthonous<br />
blocks in the Fields Creek olistostromes.<br />
Zagorcev, I., Boyanov, I. & Tikhomirova, L.B.<br />
1989. Correlation of Jurassic sections from SW Bulgaria and<br />
eastern Rhodopes by <strong>radiolaria</strong>ns complex. In: XIV Congress<br />
CBGA, abstracts. Eds.). Sofia, Bulgaria. pp. 795-798. (in<br />
Russian)<br />
Zagorcev, I., Mavridis, A., Budurov, K.,<br />
Tikhomirova, L.B., Trifonova, E., Scourtsis-<br />
Coroneou, V. & Manacos, C. 1989. New stratigraphic<br />
data on Lower Drimos Limestones (Upper Triassic) from the<br />
section of Karpenission, Pindos-Olonos Zone (Eurytania,<br />
Greece). Geol. balcan., 19/5, 3-14.<br />
The uppermost parts of the Lower Drirnos Iimestones from the<br />
section at Karpenission contain rich conodont assemblage<br />
corresponding to the middle parts of the Sevatian Epigondolella<br />
bidentata Range Zone It is dominated by the species Misikella<br />
posthernsteini Kozur & Mock and Paragondella steinbergenses<br />
Mosher, and contains the new conodont species Epigondonella<br />
postspatulata Budurov & Mavridis. A rich <strong>radiolaria</strong>n complex has<br />
been found too, it contains specific Upper Triassic taxa belonging to<br />
Spumellaria and Nassellarian including representatives of<br />
superfamily Archocyrtoidea. The foraminiferal assemblage is<br />
characterised also by taxa typical of the Upper Triassic. Red cherts<br />
from the base of the overlying cherty interval contain a <strong>radiolaria</strong>n<br />
complex of l ate Norian—Rhaetian age.<br />
Zhang, Q., Mizutani, S., Kojima, S. & Shao, J.<br />
1989. The Nadanhada Terrane in Heilongjiang Province.<br />
Geological Review, 35/1, 67-71. (in Chinese)<br />
Zhu, G. 1989. Diet analysis of Antarctic krill Euphausia<br />
superba Dana. Acta Oceanol. sinica, 8/3, 457-462.<br />
Afanasieva, M.S. 1990a. Experimental evidence for<br />
changes during fossilization of <strong>radiolaria</strong>n tests and<br />
implications for a model of biomineralization. Mar.<br />
Micropaleontol., 15/3-4, 233-248.<br />
This paper contains informations of two kinds: (1) observation<br />
on the effects of high-temperatures annealing on the organization of<br />
opaline <strong>radiolaria</strong>n test that may simulate fossilization processes<br />
and (2) an hypothetical model for the processes of formation,<br />
preservation and destruction of <strong>radiolaria</strong>n shells in geologic history,<br />
based on diverse published reports and observations of heat-treated<br />
skeletons. Biomineralization of <strong>radiolaria</strong>n skeletons start with an<br />
appearance of some primary amorphous opal globules E (0.06-0.15<br />
µm) on the hexagonal polysaccharide plates of the organic matrix.<br />
The finest globules E are grouped together, forming the globule units<br />
D (0.2-03 µm), which, in their turn, are united into a globule unit C<br />
(0.4-1 µm) .The globule units C are grouped into the hexagonal<br />
prismatic units B (1-3 µm) . The largest mineral units A (3-8 µm) are<br />
formed from the units B and pass throughout the whole shell wall.<br />
Besides that, every ultrastructural skeleton unit is surrounded by<br />
organic lamella. Therefore, the main tenement of biomineralization is<br />
corroborated: the existence of any skeleton as a single solid body is<br />
provided by the interactions of all ultrastructural skeleton elements<br />
through the unmineralized residual organic matrix.<br />
A common trend in the fossilization of skeletons is (1)<br />
destruction of the covering organic lamellae accompanied by<br />
disintegration of skeletons and (2) carbonization (tannage) of the<br />
residual organic matrix increasing a skeleton strength and silica
Bibliography - 1990 Radiolaria 14<br />
transformation in the following successional: opal-opal-tridymitetridymite-quartz.<br />
Initial stages of the secondary alteration of shells<br />
can be reconstructed by high-temperature annealing. As a result of<br />
experiment recent <strong>radiolaria</strong>n tests were partially destroyed and<br />
showed increased pore sizes, thinning of shell wall and<br />
transformation of biogenic amorphous globules into opal-tridymite<br />
and even prismatic tridymite. The annealing of <strong>radiolaria</strong>n tests from<br />
Early Permian outcrops show changing of pore sizes, cracking of<br />
skeletons along the largest ultrastructural units and besides that<br />
"guttering" of some primary globular shells and secondary<br />
crystallizing of others up to prismatic tridymite. Late Paleozoic<br />
<strong>radiolaria</strong>ns from deep drilling deposits can serve as an example of<br />
complete destruction of the carbonized organic lamellae, of an<br />
intergrowth of the mineral units and of substitution of prismatic lowtemperature<br />
tridymite by dipyramidal-prismatic low-temperature<br />
quartz. Thus, modifications of SiO2 possible can show a response to<br />
corresponding stages of lithogenesis: sedimentogenesis-diagenesisearly<br />
catagenesis-late catagenesis.<br />
Afanasieva, M.S. 1990b. Ultrastructure and secondary<br />
alterations of the <strong>radiolaria</strong>n skeleton. Paleont. Z., Akad.<br />
Nauk SSSR, 24/1, 25-36.<br />
Theoretical and experimental study of the skeleton<br />
ultrastructure of Recent and fossil <strong>radiolaria</strong>ns has made it possible<br />
to construct a model of the biomineralization and fossilization of the<br />
siliceous tests of <strong>radiolaria</strong>ns. In the biomineralization process, the<br />
primary globules of opal are grouped into progressively larger<br />
structural elements of the skeleton, each surrounded by organic<br />
lamellae. The fossilization of <strong>radiolaria</strong>n tests is accompanied by a<br />
change in I inter-relationships between the organic and the mineral<br />
components of the skeleton and by transformation of the silica in a<br />
progressive series: globular opal fi globular opal fi tridymite fi<br />
prismatic low-temperature tridymite fi dipyramidal fi prismatic lowtemperature<br />
quartz. These forms of SiO2 correspond respectively to<br />
the following stages of lithogenesis: sedimentogenesis fi diagenesis<br />
fi catagenesis fi late catagenesis.<br />
Aitchison, J. 1990. Significance of Devonian-<br />
Carboniferous <strong>radiolaria</strong>ns from accretionary terranes of the<br />
New England Orogen, eastern Australia. Mar.<br />
Micropaleontol., 15/3-4, 365-378.<br />
Radiolarians provide age constraints for many previously<br />
undated terranes in the New England Orogen (NEO), a tectonic<br />
collage developed along the eastern margin of Australia. Djungati<br />
terrane, the age range of which was previously unknown, contains<br />
two distinctive siliceous sedimentary lithofacies. The oldest is a<br />
thick sequence of red, ribbon-bedded cherts which probably<br />
accumulated in a deep ocean-floor setting far from land. Middle<br />
Silurian through Late Devonian <strong>radiolaria</strong>ns have been recovered<br />
from these cherts. Green tuffaceous cherts which contain a latest<br />
Devonian (Famennian) <strong>radiolaria</strong>n fauna depositionally overlie the<br />
lower red ribbon-bedded chert sequence. These cherts are<br />
intercalated with volcaniclastic sediments and the fauna which they<br />
contain can be used to constrain the timing of accretion of older<br />
rocks into a subduction complex.<br />
Anaiwan terrane, which was also previously undated, contains<br />
thin ribbon-bedded cherts which are depositionally overlain by<br />
tuffaceous chert, siliceous siltstones and volcaniclastic sediments.<br />
Latest Devonian (?late Famennian) and Early Carboniferous<br />
<strong>radiolaria</strong>ns have been recovered from these cherts and tuffaceous<br />
siltstones.<br />
Radiolarians also occur in fine-grained siliceous sediments of<br />
the Yarrimie Formation, part of the Gamilaroi terrane. These<br />
<strong>radiolaria</strong>ns are of Late Devonian (Frasnian) affinity and their<br />
presence indicates that blocks of limestone, which contain Givetian<br />
conodonts and corals and were previously thought to indicate the<br />
age of the Yarrimie Formation, are allochthonous.<br />
Aitchison, J. & Flood, P.G. 1990. Geochemical<br />
constraints on the depositional setting of Palaeozoic cherts<br />
from the New England orogen, NSW, eastern Australia.<br />
Marine Geol., 94/1-2, 79-95.<br />
Geochemical analyses constrain the depositional setting of two<br />
distinctive types of chert facies within two terranes of the orogen.<br />
Both chert types were conveyed into a trench by subduction<br />
processes. As subduction continued, hemipelagic sedimentation was<br />
swamped by the influx of coarse-grained volcaniclastic sediments<br />
deposited from turbidity currents reaching the trench. The diverse<br />
sedimentary types were tectonically intercalated to form sequences<br />
of imbricate thrust slices within two distinctly different subduction<br />
complexes which have subsequently been tectonically juxtaposed.<br />
Alouani, R., Tlig, S. & Zargouni, F. 1990.<br />
Découverte de radiolarites du Jurassique Supérieur dans le<br />
- 42 -<br />
"Sillon tunisien" Faciès et structures d'une marge SE de la<br />
Tethys maghrebine. C.R. Acad. Sci. (Paris), Sér. II, 310/5,<br />
609-612.<br />
Radiolarites and associated pelagic facies were deposited in an<br />
E-W directed basin at the emplacement of the so called 'Tunisian<br />
Trough, with tilted and bending blocks the movements of which were<br />
closely controlled by E-W trending strike-slip faults and N-S<br />
fractures.<br />
Amon, E.O., Braun, A. & Chuvashov, B.I. 1990.<br />
Lower Permian (Artinskian) Radiolaria from the Sim type<br />
section, Southern Urals. Geologica et Paleontologica, 24,<br />
115-137.<br />
Deposits from the Burtsevsky Horizon of the Sim section<br />
(Artinskian Stage, Southern Urals) yielded a well preserved<br />
<strong>radiolaria</strong>n fauna consisting of 23 species. Most abundant are the<br />
spherical <strong>radiolaria</strong>ns (Astroentactinia, Helioentactinia, Copicyntra,<br />
Entactinia, Entactinosphaera, Spongentactinia, Tetracircinata and<br />
Tetragregnon). Polyaxon <strong>radiolaria</strong>ns are present in minor abundance<br />
but partly with exceptionally large forms. Polyentactinia is present<br />
with two species, Albaillellaria are missing. 6 new species are<br />
described (Entactinia faceta n. sp., Entactinia? spinifera n. sp.,<br />
Spongentactinia simensis n. sp., Spongentactinia? rigida n. sp.,<br />
Tetragregnon vimineum n. sp., Ruzhencevispongus apertus n. sp.).<br />
Anderson, O.R., Bryan, M. & Bennett, P. 1990.<br />
Experimental and observational studies of <strong>radiolaria</strong>n<br />
physiological ecology: 4. Factors determining the<br />
distribution and survival of Didymocyrtis tetrathalamus<br />
tetrathalamus with implications for paleoecological<br />
interpretations. Mar. Micropaleontol., 16, 155-167.<br />
The mean growth, longevity and vitality (based on axopodial<br />
morphology and cytoplasmic flow) of Didymocyrtis tetrathalamus<br />
tetrathalamus were assessed in laboratory culture in relation to<br />
variations in temperature, salinity and light. Maximum longevity and<br />
vitality occurred in a temperature range of 21 °C to 27 °C. However,<br />
some individuals survived for extended periods (up to 18 days) with<br />
normal axopodia and cytoplasmic flow at temperatures as low as l 0 °<br />
C. Though abundant in tropical and subtropical locations and often<br />
thought to be exclusively warmer-water species, these data suggest<br />
D. tetrathalamus may have a lower temperature tolerance than<br />
indicated by it geographical location. This is in contrast to<br />
Spongaster tetras (a species found in the same locale) that is<br />
decidedly disabled by temperatures below approximately 20 ° C.<br />
Moreover, abundance of D. tetrathalamus in the natural environment<br />
near Barbados increased substantially during periods of cooler<br />
surface water temperatures associated with changes in temperature<br />
stratification of the upper water column. These data suggests that<br />
although D. tetrathalamus is typically found in low to mid latitude<br />
tropical and subtropical locations, they may not be restricted to<br />
warmer water masses assuming other environmental and trophic<br />
factors are favorable. Food vacuole contents, based on transmission<br />
electron microscopic evidence, include large proportions of diatoms,<br />
other algae and small masses of cytoplasm that lack plastids and<br />
appear to be microheterotrophs. Microflagellates (Kinetoplastida)<br />
are observed within the peripheral cytoplasm and may be consumed<br />
as prey. Eubacteria are only occasionally observed in digestive<br />
vacuoles. Partially dissolved fragments of diatom frustules are<br />
incorporated into the skeleton of D. tetrathalamus and may be used<br />
as a source of skeletal material in low silicate environments. The<br />
composite data from this research suggests that D. tetrathalamus is<br />
highly adaptive and may be capable of surviving in a broader range of<br />
trophic and physical environmental conditions than previously<br />
assumed.<br />
Anderson, O.R., Perry, C.C. & Hughes, N.P.<br />
1990. Transmission and scanning electron microscopic<br />
evidence for cytoplasmic deposition of strontium sulphate<br />
crystals in colonial <strong>radiolaria</strong>. Phil. Trans. Roy. Soc.<br />
London, 329, 81-86.<br />
Colonial Radiolaria are multicellular marine protozoa<br />
(Sarcodina) that reproduce by flagellated swarmers, each containing<br />
a vacuolar-enclosed crystal of celestite (SrSO4). The crystal<br />
morphology (an elongated square prism with pairs of triangular end<br />
faces) is unusual compared with crystals produced directly from<br />
solution. The crystals of <strong>radiolaria</strong>n swarmers are deposited within a<br />
cytoplasmic envelope, separate from the surrounding vacuolar wall,<br />
and are subsequently enclosed by an organic coat (ca. 500-1000 A<br />
thick) apparently deposited by the cytoplasmic envelope. The<br />
enclosing biological structures may account for the unusual<br />
morphology of the crystals, and offer further evidence that the<br />
process of crystallization, and ultimate crystal morphology, can be<br />
influenced markedly by surface chemistry at organo-mineral<br />
interfaces.
Radiolaria 14 Bibliography - 1990<br />
Anderson, R.Y., Linsley, B.K. & Gardner, J.V.<br />
1990. Expression of seasonal and ENSO forcing in climatic<br />
variability at lower than ENSO frequencies: evidence from<br />
Pleistocene marine varves off California. Palaeogeogr.<br />
Palaeoclimatol. Palaeoecol., 78/3-4, 287-300.<br />
Upper Pleistocene marine sediments along the upper<br />
continental slope off northern and central California contain<br />
alternations of varved and bioturbated sediments and associated<br />
changes in biota and sediment composition. These alternations can<br />
be related to conditions that accompany El Niño and anti-EI Niño<br />
(ENSO) circulation. Anti-EI Niño conditions are characterized by<br />
increased upwelling and productivity and by low concentrations of<br />
dissolved oxygen in the oxygen minimum zone that resulted in varve<br />
preservation. El Niño conditions are characterized by little or no<br />
upwelling, low productivity, and higher concentrations of dissolved<br />
oxygen that resulted in zones of bioturbation.<br />
Alternations of varves and zones of bioturbation, that range<br />
from decades to millennia, occur through the upper Pleistocene<br />
section. The inferred long-term alternations in El Niño and anti-EI<br />
Niño conditions appear to be a re-expression of ENSO's primary 3-7year<br />
cycle. Decadal to millennial cycles of productivity associated<br />
with El Niño and anti-EI Niño conditions may have served as a<br />
"carbon pump" and transferred atmospheric CO2 to the marine<br />
reservoir.<br />
Changes in sediment composition and organisms associated<br />
with El Niño or anti-EI Niño conditions can be related to both<br />
seasonal and ENSO phenomena. Expression of these changes at<br />
lower-than-ENSO frequencies may be partly explained by adding the<br />
effects of seasonal variability to effects produced by a selfoscillating<br />
ENSO system. However, deterministic mechanisms,<br />
including solar modulation of ENSO, may also contribute to long-term<br />
alternations of El Niño and anti-EI Niño conditions.<br />
Baumgartner, P.O. 1990. Genesis of Jurassic Tethyan<br />
radiolarites - The example of Monte Nerone (Umbria-Marche<br />
Apennines). In: Atti del II convegno internazionale Fossili<br />
Evoluzione Ambiente, Pergola 1987. (Pallini, G., Cecca, F.,<br />
Cresta, F. & Santantonio, M., Eds.). pp. 19-32.<br />
Recent advances in Mesozoic <strong>radiolaria</strong>n biostratigraphy have<br />
allowed to obtain detailed age data on the start and the duration of<br />
radiolarite sedimentation in four selected sections of the Monte<br />
Nerone and adjacent areas. These data, together with the rich and<br />
detailed ammonite data provided by Cecca et al. (1987a, b) Cresta<br />
et al.. (1988) etc. from the basis for a detailed sedimentation<br />
history explaining the distribution pattern of siliceous and<br />
calcareous facies on the Monte Nerone Seamount and in the adjacent<br />
basin. General conclusions on the genesis of Tethyan Jurassic<br />
radiolarites can be drawn from this well documented example. The<br />
Lower Bajocian to Lower Kimmeridgian hiatus observed on Monte<br />
Nerone is explained by vigorous periodically changing currents<br />
effectively preventing the net accumulation of sediment on the<br />
structural high. As sedimentation starts again on the high, a<br />
concomitant decrease of sedimentation rates can be observed in the<br />
adjacent basin.<br />
The local (intrabasinal) facies distribution of calcareous vs.<br />
siliceous sediments cannot be explained by regional<br />
paleoceanographic concepts. General productivity and local<br />
dispersal of calcareous and siliceous pelagic sediment at any time<br />
as well as diagenetic processes must be discussed to reasonably<br />
explain the small scale facies pattern.<br />
In Western Tethys basinal Middle Jurassic radiolarites are<br />
coeval with condensed pelagic limestones on swells. This facies<br />
contrast is not a function of the presence of a CCD. While the CCD<br />
model is consistent with the observed carbonate distribution, it does<br />
not explain occurrence and distribution of radiolarites. The absence<br />
of silica on the swell can obviously not be explained by the<br />
dissolution of carbonate at depth. Moreover, basinal facies are not<br />
solution residues of less deep swell facies, because radiolarites<br />
have much higher sedimentation rates than coeval condensed<br />
limestones on swells.<br />
It is mainly the intrabasinal dispersal of <strong>radiolaria</strong>ns which<br />
determined the local occurrence and age span of radiolarites: During<br />
the late Middle Jurassic, persistent bottom currents prevented<br />
<strong>radiolaria</strong>ns, characterized by a very low bulk density, from<br />
accumulation on the swells and carried them into the basins. The<br />
general scarcity of calcareous plankton is responsable for the<br />
formation of condensed limestones on swells and for a low carbonate<br />
input, as compared to silica, to the basins. Low concentration of<br />
calcareous plankton together with a vigorous circulation also<br />
explains shallow, irregular and sharply defined ACD and CCD.<br />
During the late Oxfordian, calcareous plankton production<br />
slowly increased and/or current activity decreased leading to an<br />
overall better carbonate preservation (= beginning of fall of ACD and<br />
CCD). Because of diminished current activity, radiolarites started to<br />
- 43 -<br />
accumulate also on the swells. This tendency continued through the<br />
Kimmeridgian and early Tithonian with a successive increase in<br />
carbonate, gradually displacing radiolarites first on the swells and<br />
then in the basins.<br />
Bechennec, F., Le Métour, J., Rabu, D.,<br />
Bourdillon de Grissac, C., De Wever, P.,<br />
Beurrier, M. & Villey, M. 1990. The Hawasina Nappes:<br />
stratigraphy, palaeogeography and structural evolution of a<br />
fragment of the south-Tethyan passive continental margin.<br />
In: The Geology and Tectonics of the Oman region.<br />
(Robertson, A.H.F., Searle, M.P. & Ries, A.C., Eds.), vol.<br />
49. Special Publications of the Geological Society of<br />
London, pp. 213-223.<br />
Lithostratigraphic and biostratigraphic revision of the Hawasina<br />
Nappes in the eastern and central Oman Mountains, including the<br />
redefinition of the Hamrat Duru Group and the definition of the three<br />
new groups, the Al Aridh, Kawr and Umar Groups, has led to a new<br />
interpretation of the palaeogeographic and structural evolution of<br />
the south-Tethyan continental margin. Margin history began in the<br />
Late Permian with a phase of extension and rifting, accompanied by<br />
considerable magmatic activity, and led to the development of the<br />
Hamrat Duru Basin separating the Arabian Platform to the south<br />
from the Baid Platform to the north. In the Middle to Late Triassic<br />
renewed extension led to rifting, again accompanied by important<br />
magmatic activity, with the break-up of the Baid Platform, and the<br />
development of the Al Aridh Trough, the Misfah Horst and the Umar<br />
Basin. These Permian and Triassic tectonic units together<br />
constituted the Hawasina Basin. A third phase of extension during<br />
the Late Tithonian-Berriasian caused a general foundering of the<br />
continental margin. The development of the Hawasina Basin<br />
terminated in the Santonian, when compression initiated the first<br />
fase of obduction that closed the basin. Ongoing obduction, during<br />
the Campanian, led thrusting of the Hawasina and the Samail<br />
ophiolite nappes onto the Arabian Platforn by gravitational<br />
mechanisms.<br />
Berdnikov, V.A. 1990. Quaternary stratigraphy of the<br />
Central Basin of the indian Ocean as indicated by Radiolaria.<br />
Oceanology, 29/4, 469-473.<br />
Detailed analysis of <strong>radiolaria</strong>n complexes in cores from the<br />
Central basin of the Indian Ocean distinguishes four layers,<br />
corresponding to the <strong>radiolaria</strong>n zones in the Nigrini zonal scale<br />
(1971). Some 136 species of <strong>radiolaria</strong>n were determined and<br />
counted in 320 sediment samples. The age of the core sediments is<br />
determined. Two intervals representing periods of cooling are<br />
identified in each of the cores.<br />
Bernstein, R.E., Betzer, P.R. & Takahashi, K.<br />
1990. Radiolarians from the western North Pacific Ocean: a<br />
latitudinal study of their distribution and fluxes. Deep-Sea<br />
Res. Part A, oceanogr. Res. Pap., 37/11, 1677-1696.<br />
Free-drifting sediment traps were deployed individually to make<br />
day-long collections of settling particulates at seven stations in the<br />
western North Pacific Ocean. Samples were taken between 70 and<br />
2200 m along a longitudinal section between 16 and 50°N latitude.<br />
Radiolarian skeletons were mechanically isolated under a reflected<br />
light microscope. Subsequent gravimetrically determined <strong>radiolaria</strong>n<br />
silica fluxes range from 0 to 4.43 mg m -2 day -1 and show<br />
significant and consistent increases at all depths with increasing<br />
latitude. Radiolarians also were counted and categorized into each of<br />
their three suborders: Nassellaria, Spumellaria and Phaeodaria. An<br />
inverse relationship is evident between the proportions of<br />
phaeodarians and polycystines (nassellarians plus spumellarians),<br />
with the phaeodarians increasing relative to the polycystines with<br />
increasing latitude.<br />
Although the absolute numbers of phaeodarians in the northern<br />
samples may not exceed the numbers of their polycystine<br />
counterparts in the south, the comparatively large and heavy<br />
phaeodarian skeletons contribute significantly to the increased<br />
silica fluxes noted in the north. This contribution, combined with a<br />
high susceptibility to dissolution, may signify that phaeodarians are<br />
important for the recycling of silica in the northern North Pacific.<br />
Spectrophotometric analyses of seven phaeodarian species and<br />
one species of colonial spumellarian show that silica constituted<br />
between 86 and 99% of the phaeodarians' skeletons and 75% of the<br />
spumellarians' skeletons. Non-<strong>radiolaria</strong>n amorphous silica was<br />
mobilized by a selective chemical leach and quantified<br />
spectrophotometrically. Significant and consistent increases in the<br />
flux of this diatomaceous silica fraction (ranging from 0.14 to 47.0<br />
mg m -2 day -1 ) are noted with increasing latitude. In almost all cases,<br />
diatomaceous silica fluxes are greater than those of the<br />
<strong>radiolaria</strong>ns. With the exception of some anomalously high<br />
percentages, <strong>radiolaria</strong>n-derived silica ranges from 0 (only one<br />
sample) to 24% of the total amorphous silica flux.
Bibliography - 1990 Radiolaria 14<br />
Blueford, J.R., Gonzales, J.J. & Van Scoy, K.<br />
1990. Comparing <strong>radiolaria</strong>n and diatom diversity and<br />
abundance from the northeast Pacific. Mar. Micropaleontol.,<br />
15/3-4, 219-232.<br />
Particle trap samples (VERTEX) from 4 locations in the<br />
northeast Pacific were used to compare centric and pennate diatoms<br />
with nassellarian and spumellarian <strong>radiolaria</strong>ns. The proportion of<br />
pennates and nassellarians were highest at VERTEX3 from the<br />
northeast tropical oceans, off the west coast of Mexico. Colonial<br />
<strong>radiolaria</strong>ns were characteristic of warm, high saline waters from the<br />
southern edge of the north Pacific central gyre, north of Hawaii<br />
(VERTEX4), while pennate diatoms were abundant. The subtropic<br />
oceanic Pacific (VERTEX5A) had more pennate diatoms, while<br />
VERTEX(5C), in a coastal cyclonic eddy located west of California,<br />
had an even proportion of centric and pennate diatoms. Comparison<br />
of major faunas and flora at various oceanic sites of present<br />
siliceous sedimentation in conjunction with atmospheric,<br />
hydrographic and chemical data, can be helpful in reconstructing<br />
paleoceanographic and paleoenvironmental conditions of the past<br />
oceans throughout the Phanerozoic.<br />
Bourgois, J., Eguez, A., Butterlin, J. & De<br />
Wever, P. 1990. Evolution géodynamique de la Cordillère<br />
Occidentale d'Equateur : la découverte de la formation Eocène<br />
d'Apagua. C.R. Acad. Sci. (Paris), Sér. II, 311, 173-180.<br />
Braun, A. 1990. Evolutionary trends and biostratigraphic<br />
potential of selected <strong>radiolaria</strong>n taxa from the Early<br />
Carboniferous of Germany. Mar. Micropaleontol., 15/3-4,<br />
351-364.<br />
A large number of well preserved <strong>radiolaria</strong>n faunas have been<br />
found in Early Carboniferous rocks (Pericyclus-Alpha to Goniatites-<br />
Stufe) of the "Rheinisches Schiefergebirge" and the Frankenwald<br />
(Germany). The growing number of fossil faunas makes it possible to<br />
show evolutionary tendencies of certain taxa within these<br />
stratigraphic levels. In the course of the Early Carboniferous a<br />
continuous transformation of the general character of the<br />
<strong>radiolaria</strong>n faunas took place. This transformation generally tended<br />
towards an increase of the surface area of the skeletons. We see<br />
trends within the following groups.<br />
The Entactiniidae Riedel 1967 show two separate tendencies,<br />
one being a considerable lengthening of their spines, the other being<br />
a reduction of spine-number connected with a strong increase in size<br />
of the remaining spines.<br />
The Albaillellidae Deflandre 1973 show a documentable change<br />
in the morphology of their cavea as well as their stapia.<br />
The Latentifistulidae Nazarov and Ormiston 1983 evolve from<br />
ancestral narrow-rayed forms to broad-triradiate and triangular<br />
forms.<br />
The "phacoid" forms of the group Sphaerodiscus Won<br />
1983/Eostylodictya Ormiston and Lane 1976 show a progressive<br />
overgrowth of the central shell by peripheral concentric rings and a<br />
simultaneous change in morphology from flat-discoidal to lensoid.<br />
Budai, T. & Dosztály L. 1990. Stratigraphic problems<br />
associated with the Ladinian formations in the Balaton<br />
Highland. M. All. Földtani Intézet évi jelentése, 61-79. (in<br />
Hungarian)<br />
A rich Cordevolian <strong>radiolaria</strong>n assemblage was identified from<br />
the Szaka-negy quarry at Balatonfured, where limonitized skeletons<br />
were preserved in a fairly good state. The assemblage identified<br />
from the Fured Limestone shows a rather great similarity to the<br />
fauna described from Gostlingen in Austria (KOZUR—MOSTLER,<br />
1979, 1981). From among the borehole profiles the borehole<br />
Mencshely Met. 1 was the only one allowing us to draw the<br />
Ladinian—Carnian boundary, on the basis of <strong>radiolaria</strong>ns, within one<br />
sequence. The Plafkerium cochleata species identified from the<br />
Buchenstein Formation clearly refers to the Longobardium, whereas<br />
the <strong>radiolaria</strong>n assemblage of the Fured Limestone is Cordevolian<br />
here, too.<br />
Cachon, J., Cachon, M. & Estep, K.W. 1990.<br />
Phylum Actinopoda Classes Polycystina (= Radiolaria) and<br />
Phaeodaria. In: Handbook of Protoctista. (Margulis, L.,<br />
Corliss, J.O., Melkonian, M. & Chapman, D.J., Eds.), The<br />
Jones and Barlett Series in Life Sciences. Jones and Barlett<br />
Publishers, Boston. pp. 334-346.<br />
The actinopods are heterotrophic protoctists; their cells bear<br />
long processes called axopods which develop from specialized<br />
structures called axoplasts. The protoctists to be covered in this<br />
chapter were originally classified as four "tribes" within a single<br />
- 44 -<br />
class, the Radiolaria (Haeckel, 1887). Recent recognition of<br />
diversity within the group has led to the rejection of the term<br />
Radiolaria as the name for a formal taxon. These organisms are now<br />
divided into two classes within the phylum Actinopoda, the<br />
Polycystina and Phaeodaria (Riedel, 1967). Phylum Actinopoda also<br />
includes the heliozoans and acantharians, to be covered in<br />
subsequent sections of this chapter. The actinopods are<br />
characterized by their axopods, which radiate from the cell surface<br />
and are involved in prey capture. Represented here are some of the<br />
largest protoctists; solitary individuals are 30 µm to 2 mm and<br />
colonies can be as long as several meters (Anderson, 1983).<br />
Members of the class Polycystina are characterized by regularly<br />
perforated silica skeletons with radial axopods emerging among fine,<br />
ramified pseudopods (Fig. 1). Pseudopods are fine cytoplasmic<br />
projections serving specialized functions. They are sometimes<br />
stiffened by a central cytoskeletal axis. Surrounding the skeleton<br />
and axopods is a thin layer of cytoplasm in which mitochondria and<br />
refractile granules exhibit saltatory motion. Members of the class<br />
Phaeodaria sometimes lack skeletons; when present, the skeleton<br />
consists of isolated pieces or numerous hollow tubes. Besides<br />
differences in skeletal structures, polycystines and phaeodarians<br />
also differ in ultrastructural body plan. Individuals of both classes<br />
are predatory on nannoplankton mastigotes, diatoms, and copepods.<br />
A number of polycystines contain algal symbionts. Organisms within<br />
these classes are both uni- and multinucleated and, along with the<br />
ciliates and foraminifera, exhibit multiple nuclear division (Hollande<br />
et al., 1969). Reproduction in many species appears to occur<br />
exclusively by multiple fission (Hollande and Enjumet, 1953;<br />
Sieburth, 1979), producing mastigotes ("swarmer cells") with two<br />
undulipodia (Hollande and Enjumet, 1953; Cachon-Enjumet, 1964).<br />
Sexual reproduction has not been observed.<br />
Caron, D.A. & Swanberg, N.R. 1990. The ecology of<br />
planktonic sarcodines. Rev. Aquatic Sci., 3/2-3, 147-180.<br />
Planktonic sarcodines (amoebae, foraminifera, and actinopoda)<br />
are a taxonomically diverse and ecologically important component of<br />
oceanic plankton food webs. In addition, the fossilizable tests<br />
produced by many of these protist species have been, and continue<br />
to be, extensively used as an important tool for reconstructing<br />
paleoclimatological conditions. Living planktonic sarcodines,<br />
however, have not been as intensively studied as their nonliving<br />
remains. Biological oceanographers have been slow to recognize the<br />
potential importance of planktonic sarcodines in the flow of energy<br />
and materials in the marine plankton because of the complex trophic<br />
status of these organisms and their fastidious nature in laboratory<br />
culture. Only recently has there been a realization that these<br />
organisms may contribute significantly to photosynthesis (via<br />
symbiotic algae sequestered within the cytoplasm), total grazing<br />
pressure in the plankton, and the total flux of material to the deep<br />
ocean. In this paper, the existing data on the abundance, trophic<br />
interactions, and grazing rates of planktonic sarcodines are<br />
summarized and reviewed. Based on this reevaluation, it is<br />
suggested that these protists play a potentially important role in the<br />
cycling of energy and material in oceanic plankton communities.<br />
Carter, E.S. 1990. New biostratigraphic elements for<br />
dating upper Norian strata from the Sandilands Formation,<br />
Queen Charlotte Island, British Columbia, Canada. Mar.<br />
Micropaleontol., 15/3-4, 313-328.<br />
Upper Norian <strong>radiolaria</strong>ns have been recovered from the basal<br />
Sandilands Formation on northwest Graham Island (Kennecott Point<br />
), Kunga Island, and Louise Island, Queen Charlotte Islands. Rare<br />
conodonts and ammonoids are associated with the <strong>radiolaria</strong>ns at<br />
several levels.<br />
At Kennecott Point over 90 m of the lower Sandilands<br />
Formation is coarser and less tuffaceous than is typical of the<br />
formation elsewhere and appears to represent continuous<br />
sedimentation. Diverse, well preserved <strong>radiolaria</strong>ns have been found<br />
in limestone concretions in the lower 75 m of section which has also<br />
yielded conodonts from the Epigondolella bidentata Zone<br />
(approximates Cordilleranus to basal Crickmayi ammonoid zones)<br />
and ammonoids from the Crickmayi Zone.<br />
At Kunga Island in the southern Queen Charlotte Islands,<br />
excellent <strong>radiolaria</strong>n faunas have also been recovered from a 30 m<br />
interval beginning 80 m above the final occurrence of Monotis ( =<br />
Cordilleranus Zone ) and from a second 90 m interval Iying<br />
structurally above the former that contains the upper Norian<br />
conodont Epigondolella bidentata at the base.<br />
Three preliminary <strong>radiolaria</strong>n assemblages are recognized for<br />
upper Norian strata Iying above the Monotis beds. Assemblage 1, the<br />
lower one, is tentatively correlated with the upper part of the<br />
Cordilleranus Zone; Assemblage 2 approximates the Amoenum Zone<br />
and Assemblage 3 is correlated with the Crickmayi Zone.<br />
The age of the Sandilands Formation is now confirmed to be late<br />
Norian and Hettangian as well as Sinemurian. Considering the record
Radiolaria 14 Bibliography - 1990<br />
of apparently uninterrupted sedimentation, the section thickness<br />
and the excellent fossil recovery, the Sandilands Formation has been<br />
shown to contain an unusually thick upper Norian sequence and<br />
probably the Triassic-Jurassic boundary.<br />
Carter, E.S. & Galbrun, B. 1990. A preliminary note<br />
on the application of magnetostratigraphy to the Triassic-<br />
Jurassic boundary strata, Kunga Island, Queen Charlotte<br />
Islands, British Columbia. Geol. Surv. Canada, curr. res.,<br />
Pap., 90-1F, 43-46.<br />
One hundred and five, 2.5 cm diameter, oriented cores were<br />
obtained from Triassic-Jurassic strata of the Sandilands Formation<br />
on Kunga Island in July 1989.<br />
Casey, R.E., Weinheimer, A.L. & Nelson, C.O.<br />
1990. Cenozoic <strong>radiolaria</strong>n evolution and zoogeography of<br />
the Pacific. Bull. marine Sci., 47/1, 221-232.<br />
Modern day <strong>radiolaria</strong>n distributions can be grossly divided into<br />
warm and cold water spheres separated by the polar convergences<br />
and the associated pycnocline. During the Paleogene both warn and<br />
cold water sphere <strong>radiolaria</strong>n diversities appear to have been lower<br />
than during the Neogene. One major reason for this difference<br />
appears to be the difference in the number of "packages" of water<br />
(water masses essentially) for <strong>radiolaria</strong>ns to inhabit during these<br />
times. The number of "packages" or provinces increased in the<br />
Neogene due to the development of polar convergences and their<br />
associated polar, shallow subpolar and intermediate waters, the<br />
initiation of the formation of Antarctic (Polar) Bottom Water and<br />
associated Circumpolar Water, and the development of the surface<br />
Eastern Tropical Pacific as a specific "package" of water. Specific<br />
examples of <strong>radiolaria</strong>ns evolving into these packages support these<br />
contentions. Another Neogene development was the creation of a<br />
new "package" that apparently resulted in the evolution, or<br />
expansion, of a new niche, that of the symbiont bearing <strong>radiolaria</strong>ns<br />
by a variety of taxa. This apparently was preceded by changes in<br />
Antarctic geographies (and perhaps some biological influences) that<br />
resulted in Antarctic glaciation and the development of this niche.<br />
Chang, K.H., Woo, B.G., Lee, J.H., Park, S.O. &<br />
Yao, A. 1990. Cretaceous and Early Cenozoic Stratigraphy<br />
and history of Eastern Kyongsang Basin, S. Korea. Jour.<br />
geol. Soc. Korea, 26/5, 471-487.<br />
A detailed stratigraphic work has made it possible to<br />
reconstruct the geology of the both sides of the Yangsan fault to the<br />
pre-fault state. The dextral motion of the fault of about 35 km is<br />
obvious since the geology fits very well if the eastern block is<br />
rearranged about 35 km northward. Such a restoration shows the<br />
original (i.e., pre-faulting) Yongyang subbasin characterized by the<br />
Yongyang-type stratigraphic scheme of the Hayang Group. This<br />
scheme is no more applicable beyond the southern boundary of the<br />
so-reconstructed Yongyang subbasin. The Eocene acidic tuff<br />
apparently was dissected by the Yangsan fault, which in turn was<br />
concealed by the mid-Miocene sedimentation.<br />
The northern peripheral part of the Yongyang subbasin is<br />
dislocated due to the Yangsan and the associated faults. But, a prefault<br />
reconstruction has figured out an east-west trending<br />
"Pyonghae trough" in which the Kyongjongdong and the Ullyonsan<br />
Formations deposited. It is presumed that the north-bounding scarpmaking<br />
growth fault of the trough was forming but later turned into a<br />
reverse fault now called the "llwol thrust".<br />
A paleocurrent analysis with 158 cross-stratifications of the<br />
Kyongjongdong Formation and the overlying Hayang Group indicates<br />
a mean source area in the direction of N 54° E. Derived therefrom,<br />
reddish and variegated <strong>radiolaria</strong>n chert pebbles abundantly occur in<br />
two separate intervals of the Hayang Group. The <strong>radiolaria</strong>ns<br />
secured from the chert pebbles range in age from Middle Permian to<br />
Early Jurassic. Coeval radiolarites, not at all found on Korean<br />
peninsula, are widely distributed in the Tamba-Mino-Ashio and<br />
Chichibu belts of Japan. Some of these belts may have been the<br />
source area of the study area.<br />
Cox, B.M. 1990. A review of Jurassic Chronostratigraphy<br />
and age indicators for the UK. In: Tectonic events responsible<br />
for Britain's oil gas reserves. (Hardman, R.F.P. & Brooks, J.,<br />
Eds.), vol. 55. Special Publications of the Geological<br />
Society of London, London, U.K. pp. 169-190.<br />
The basis of the chronostratigraphic subdivision of the Jurassic<br />
System is the sequence of ammonite faunas. At present, the 11<br />
Jurassic stages (representing approximately 70 million years) can<br />
be divided into 145 ammonite-based zones or subzones. Methods of<br />
subdivision and correlation by various microfossil groups have also<br />
been developed for practical and economic reasons. Dating by<br />
fossils (biostratigraphy) underpins the broader-based approachs of<br />
- 45 -<br />
event and sequence stratigraphy. It also supplies the primary<br />
stratigraphic control in the development of a standard magnetic<br />
polarity time-scale (magnetostratigraphy) of global applicability. At<br />
present, the Jurassic System of the UK area is divided into 38 units<br />
(biozones and subzones) on the basis of dinoflagellate cysts and 23<br />
on the basis of calcareous nannofossils. Coverage is less<br />
comprehensive using the benthonic groups (foraminifera and<br />
ostracoda) which are more affected by environmental controls. The<br />
Lower Jurassic is divided into 16 units on the basis of foraminifera,<br />
but higher in the System only local divisions can be recognised in the<br />
Bathonian and informal divisions in the Callovian and oldest<br />
Oxfordian. There is fuller but still incomplete coverage using<br />
ostracoda which have proved particularly useful in the non-marine,<br />
brackish and marginal marine sequences of the Bathonian and<br />
Portlandiam The recovery of <strong>radiolaria</strong> from Jurassic sediments in<br />
the UK arca is a new an(l exciting development which allows division<br />
of Kimmeridgian and Portlandian strata in graben areas in the North<br />
Sea Basin.<br />
Danelian, T. & Baudin, F. 1990. Découverte d'un<br />
horizon carbonaté, riche en matière organique, au sommet des<br />
radiolarites d'Epire (zone ionienne, Grèce): le Membre de<br />
Paliambela. C.R. Acad. Sci. (Paris), Sér. II, 311, 421-428.<br />
A litho- and biostratigraphical study performed on a carbonated<br />
sequence from north-western Greece, allows a definition of a new<br />
member on the top of the Upper Jurassic series from the Ionian zone:<br />
the Paliambela Member. This Member is paleontologically dated from<br />
the Middle Oxfordian to the Lower Tithonian and is mainly composed<br />
of organic-rich micrites with Radiolaria and thin Bivalves. It is the<br />
first characterization of organic-rich sequence in the Callovian-<br />
Kimmeridgian in the Ionian zone, which probably has a localized<br />
paleogeographical meaning.<br />
De Wever, P., Bourdillon de Grissac, C. &<br />
Bechennec, F. 1990. Permian to Cretaceous <strong>radiolaria</strong>n<br />
biostratigraphic data from the Hawasina Complex, Oman<br />
Mountains. In: The Geology and Tectonic of the Oman<br />
Region. (Robertson, A.H.F., Searle, M.P. & Ries, A.C.,<br />
Eds.), vol. 49. Special Publications of the Geological<br />
Society of London, pp. 225-238.<br />
The analysis of foraminifera and <strong>radiolaria</strong> in 3000 carbonate<br />
and 150 siliceous rock samples from the Oman Mountains results in<br />
revision of the existing stratigraphy and supports the definition of<br />
new units. In the Hawasina allochthonous unit the main results are as<br />
follows: (i) Permian bedded chert exists near the base of the<br />
sequence and is thus the first Permian bedded chert occurrence<br />
reported from the Tethyan region); (ii) an important volcanic event is<br />
dated as Triassic; (iii) bedded chert horizons are dated as Liassic;<br />
(iv) the thick turbiditic sequence has been divided into several units<br />
of Middle and Late Jurassic age. In the Samail ophiolite: (i) the ages<br />
of four tectonic episodes were established from the beginning of<br />
oceanic spreading (Albian—Early Cenomanian), to the obduction of<br />
the ophiolitic nappe (Campanian)<br />
De Wever, P., Caulet, J.P. & Bourgois, J. 1990.<br />
Radiolarian biostratigraphy from Leg 112 on the Peru<br />
margin. In: Proceedings of the Ocean Drilling Program,<br />
Scientific Results. (Suess, E., Von Huene, R. et al., Eds.),<br />
vol. 112. College Station, TX (Ocean Drilling Program), pp.<br />
181-207.<br />
The <strong>radiolaria</strong>n fauna found at the 10 sites drilled during Ocean<br />
Drilling Program (ODP) Leg 112 range in age from Eocene to<br />
Holocene. Relatively abundant and well-preserved assemblages are<br />
present in Sites 682, 683, 685, and 688. Occurrence tables of 175<br />
species are presented for these sites. For each site, stratigraphic<br />
results are summarized in two figures showing the <strong>radiolaria</strong>n<br />
biozonation, the inferred hiatuses, and barren intervals. The<br />
Pliocene/Pleistocene and Miocene/Pliocene boundaries were not<br />
recognized from <strong>radiolaria</strong>n stratigraphy. Pleistocene and middle<br />
Miocene <strong>radiolaria</strong>n assemblages are generally abundant and well<br />
preserved. New stratigraphic data are given for some rarely<br />
described species, such as Cypassis irregularis, Lamprocyrtis<br />
daniellae, Plectacantha cresmatoplegma, Pterocanium grandiporus,<br />
Pseudocubus warreni, and Phormostichoartus (?) crustula.<br />
De Wever, P., Martini, R. & Zaninetti, L. 1990.<br />
Datation paléontologique des radiolaires du Lagonegro<br />
(Formation du Monte Facito, Italie méridionale).<br />
Individualisation dès le Trias moyen de bassins pélagiques en<br />
Téthys occidentale. C.R. Acad. Sci. (Paris), Sér. II, 310,<br />
583-589.<br />
Divakar-Naidu, P. 1990. Distribution of upwelling index<br />
planktonic foraminifera in the sediments of the western
Bibliography - 1990 Radiolaria 14<br />
continental margin of India. Oceanologica Acta, 13/3, 327-<br />
333.<br />
Twenty-one surficial sediment samples were analysed for<br />
planktonic foraminifers, <strong>radiolaria</strong>ns, calcium carbonate and organic<br />
carbon. The distribution of these parameters suggest that the<br />
sediments record an upwelling signature. Q-mode factor analysis of<br />
twenty-two planktonic foraminifera species reveals four<br />
assemblages accounting for 96% of the information given in the<br />
original data matrix. Based on the distribution of factor loadings, the<br />
frequency of Globigerina bulloides in the sediments can be used to<br />
reconstruct the intensity of past upwelling in the Arabian Sea.<br />
Dunbar, R.B., Mucciarone, D., Jones, B.,<br />
Leventer-Reed, A.R., Pyne, A.R. & Moser, C.<br />
1990. Biogenic sediments fluxes in the western Ross Sea.<br />
Antarct. J. U. S., 25/5, 100-102.<br />
Although it is clear that deep shelf currents play a major role in<br />
the redistribution of biogenic phases on the antarctic margin, the<br />
extent to which photic-zone and mid-water-column processes<br />
control the flux of organic debris to the seafloor is not yet known. A<br />
major impediment to a more complete understanding of the fluxes of<br />
key elements like carbon, nitrogen, silicon, and phosphorus in the<br />
southern ocean water column has been the absence of year-round<br />
environmental monitoring and sampling. Our principal goal during the<br />
1989-1990 field season was to install four sets of time-series<br />
sediment traps on winter-over moorings in the western Ross Sea. We<br />
also recovered winter-over moorings equipped with current meters<br />
and single-cup sediment traps and completed a sediment collection<br />
program in Granite Harbor.<br />
Our field work was conducted from the sea ice during<br />
November, 1989, and aboard the R/V Polar Duke during January and<br />
February, 1990. On Polar Duke, we deployed six time-series (15<br />
cups) sediment traps at three sites in the western Ross Sea. These<br />
deployments are part of an interdisciplinary, multi-institutional<br />
study of the biogeochemical cycles of silicon and carbon in the Ross<br />
Sea. The sediment traps will be deployed for 2 years and will provide<br />
the first view of sediment fluxes over a monthly time-scale<br />
throughout the austral winter and summer in the Ross Sea. These<br />
results will complement the water-column production and recycling<br />
studies of organic matter (W. Smith, University of Tennessee) and<br />
biogenic silica (D. Nelson, Oregon State University), and the shelf<br />
current and seafloor sediment studies of D. DeMaster (North<br />
Carolina State University) and C. Nittrouer (State University of New<br />
York at Stonybrook). The mooring sites (table 1) were located at the<br />
ends of sampling transects which traverse areas ranging from icefree<br />
to heavily ice-covered during most of the austral summer.<br />
Mooring A is located in a region of highly biosiliceous seafloor<br />
sediment (greater than 40 percent opal; Dunbar et al. 1985) and in<br />
which a large ice-edge bloom was encountered<br />
Farimond, P., Eglinton, G. & Brassell, S.C. 1990.<br />
The Cenomanian-Turonian anoxic event in Europe; an<br />
organic geochemical study. Marine Petroleum Geol., 7/1, 75-<br />
89.<br />
Thirty-two sediment samples, mainly. black shales from<br />
Cenomanian/Turonian organic-rich sequences in Europe and Tunisia,<br />
were examined by organic geochemical techniques. The results of<br />
molecular analyses indicate that all the black shales are dominated<br />
by marine-derived organic matter from both algal and bacterial<br />
sources, with only a minor terrestrial component. Oxygen-deficient<br />
conditions prevailed during the deposition of the black shales,<br />
although interbedded non-laminated, organic-lean horizons indicate<br />
that oxygen deficiency was intermittent at some sites. The presence<br />
of 17 α (H), 18 α (H), 21 β (H)-28, 30-bisnorhopane in some black<br />
shale samples from shallow shelf areas may be evidence for<br />
severely oxygen-depleted conditions, possibly in association with<br />
upwelling and an oxygen-minimum layer. Overall, the organic<br />
geochemical data are in agreement with a depositional model<br />
whereby an oxygen-minimum layer developed in response to high<br />
surface productivity. This oxygen-minimum layer may have extended<br />
over a considerable thickness of the water column (>1000 m) in<br />
some areas. We report the first observation of an A-ring methylated<br />
C29 hopane, namely methyl-17 α (H), 18 α (H), 21 β (H)-28, 30bisnorhopane.<br />
The environmental significance of this compound<br />
cannot yet be assessed, although in the sample in which it occurs,<br />
the direct parallel between the carbon number distribution of the<br />
hopanes and that of the methylhopanes suggests either that they<br />
have the same biological origin or that methylation of hopanoids may<br />
have occurred, possibly during diagenesis.<br />
Faure, M. & Ishida, K. 1990. The mid-Upper Jurassic<br />
olistostrome of the west Philippines: a distinctive keymarker<br />
for the North Palawan block. J. Southeast Asian Earth<br />
Sc., 4/1, 61-67.<br />
- 46 -<br />
A field survey in North Palawan shows that this part of the<br />
island is mainly occupied by a chaotic clastic sequence in which<br />
several facies are distinguished; namely turbidite and slump<br />
deposits, pebbly mudstone, thick coarse sandstone and<br />
olistostrome, with exotic blocks of Permian or Triassic chert and<br />
limestone Mid-Upper Jurassic Limestone, acidic lava and<br />
volcanoclastic rocks. Callovian to Lower Kimmeridgian <strong>radiolaria</strong>n<br />
assemblages have been discovered from the mudstone matrix.<br />
Combining our new results with previous stratigraphic data, it is<br />
likely that the olistostrome with exotic blocks is followed by late<br />
Cretaceous-Eocene (?) turbidites. The same kind of olistostrome is<br />
known from the Calamian, Mindoro, Panay and Carabao islands. We<br />
propose that this olistostrome can be used as a distinctive criteria<br />
of the Palawan block. Comparisons of the age range of the matrix<br />
and the nature of the olistoliths suggest that the Palawan<br />
olistostrome can be correlated with the Sanbosan zone of S.W. Japan<br />
and central Ryukyu. To the south, such an Upper Jurassic<br />
olistostrome has not yet been recognized, though it is probably<br />
present below the chert-spilite formation of Borneo.<br />
Febvre, J. 1990. Phylum Actinopoda Class Acantharia. In:<br />
Handbook of Protoctista. (Margulis, L., Corliss, J.O.,<br />
Melkonian, M. & Chapman, D.J., Eds.), The Jones and<br />
Barlett Series in Life Sciences. Jones and Barlett Publishers,<br />
Boston. pp. 363-379.<br />
The Acantharia, comprising about 50 genera and 150 species<br />
in 20 families grouped into 4 orders,-display relatively little<br />
diversity. Systematics are given in Schewiakoff (1926) and<br />
Rechetniak (1981). They are unicellular phagotrophic actinopods<br />
which have three main distinctive characters: (i) skeletons of<br />
strontium sulfate (celestite) that exhibit a strictly defined<br />
configuration of 10 diametral or 20 radial spicules diverging<br />
according to Muller's law (Muller, 1858) (Fig. l); (ii) cell body<br />
covered with an outer pellicle, the periplasmic cortex (Febvre, 1972,<br />
1974), composed of at least 20 polygonal parts centered around<br />
the apex of each spicule and joined to one another by elastic<br />
junctions (Febvre 1973); and (iii,' the possession of numerous<br />
ribbonlike or cylindrical motile organelles called myonemes<br />
composed of dense bundles of 3 nm microfilaments, each of which is<br />
connected by one end to the tip of the spicule and by the other end<br />
to the periplasmic cortex (Fig. 2, 3) (Febvre, 1971). Although they<br />
form cysts and mastigotes, sexual life cycles have never been<br />
described.<br />
Febvre, J., Febvre-Chevalier, C. & Sato, H. 1990.<br />
Polarizing microscope study of a contractile nanofilament<br />
system: the Acantharian myoneme. Biol. Cell, 69, 41-51.<br />
Birefringence changes have been studied during the<br />
contraction—relaxation cycle of the myonemes (contractile<br />
organelles consisting of a bundle of nonactin filaments) in<br />
Acantharians (Protista, Actinopoda). Myonemes can either contract<br />
rapidly or undulate slowly between their anchorage points. In thin<br />
sections they appear as a large cross-striated bundle with long clear<br />
zones (LZs) and thin transversal dense bands (TBs). The filaments<br />
(2-4 nm in diameter) are twisted in pairs in elementary<br />
microstrands. The spacing of the LZ depends on the extent of<br />
contraction [161. A negative birefringence has been seen in vivo<br />
and in vitro. In vivo, retardation varied with the extent of relaxation<br />
of the myoneme (2.5 nm-4.4 nm). When the myoneme was<br />
tightened, it appeared to be homogeneously dark or bright in<br />
contrast depending on the orientation for the vibrating plane of<br />
polarized light. When it was partially relaxed and moved slowly, a<br />
series of birefringent bands, 0.8-2.8 µm thick, could be seen. They<br />
propagated at the same speed (about 2 µm-s -1 ) by successive<br />
trains, either forward or backward. Each of these birefringent bands<br />
may correspond to 4-13 contracted LZs. It is suggested that the<br />
negative birefringence of the myoneme is mainly caused by the<br />
orientation of the filaments forming the microstrands. Our results<br />
strongly suggest that the orientation of the myoneme filaments is<br />
altered during the movement an-l that the orientation of the<br />
filaments in the negative bands is caused by perpendicular<br />
orientation compared to the other parts of the myoneme. These<br />
observations support our previous hypothesis in which we postulated<br />
that the length of the myoneme varies in relation to the pitch of the<br />
elementary microstrands.<br />
Febvre-Chevalier, C. 1990. Phylum Actinopoda Class<br />
Heliozoa. In: Handbook of Protoctista. (Margulis, L.,<br />
Corliss, J.O., Melkonian, M. & Chapman, D.J., Eds.), The<br />
Jones and Barlett Series in Life Sciences. Jones and Barlett<br />
Publishers, Boston. pp. 347-362.<br />
The Heliozoa are a small group of predaceous heterotrophic<br />
actinopods, spherical unicells having naked, organic, or siliceous<br />
coated bodies from which long axopods radiate. Axopods, underlain<br />
by a microtubular axoneme, are used as organelles of locomotion and<br />
feeding. About 34 genera and more than 90 species have been
Radiolaria 14 Bibliography - 1990<br />
reported (Rainer, 1968; Bardele, 1977; Thomsen, 1978; Shigenaka<br />
et al., 1980; Febvre-Chevalier, 1982). The heliozoa, once called<br />
"sun animalcules" are divided into two orders: Cryptaxohelida and<br />
Phaneraxohelida, each comprising four suborders (Febvre-Chevalier<br />
and Febvre, 1984). Eleven families can be recognized from the 14<br />
genera so far examined ultrastructurally. Sexual processes have<br />
been reported in two species.<br />
Fourcarde, E., Azema, J., De Wever, P. &<br />
Busnardo, R. 1990. Contribution à la datation de la croûte<br />
océanique de l'Atlantique central: Age Valanginien inférieur<br />
des basaltes océaniques et âge Néocomien des calcaires<br />
maiolica de Maio (Iles du Cap Vert). Marine Geol., 95/1, 31-<br />
44.<br />
The discovery of calpionellids and <strong>radiolaria</strong>ns in thin<br />
sedimentary layers intercalated in the upper part of MORB tholeiitic<br />
pillow basalts allows us to date the oceanic crust of Maio Island<br />
(Cape Verde Islands) as early Valanginian instead of, as was hitherto<br />
believed Late Jurassic. This new dating fits better with<br />
reconstructions of the geological history of the central Atlantic<br />
based on magnetic anomalies. The overlying light-coloured pelagic<br />
limestones (Maiolica facies) with <strong>radiolaria</strong>ns, apatychi and<br />
ammonites are Valanginian-Barremian in age. These limestones are<br />
lithologically similar to the white limestones drilled at several DSDP<br />
sites in the central Atlantic.<br />
Fukudomi, T. 1990. Jurassic melange, Kanoashi Complex,<br />
western Shimane Prefecture, southwestern Japan. J. geol.<br />
Soc. Japan, 96/8, 653-667. (in Japanese)<br />
The Kanoashi Complex in the western part of Shimane<br />
Prefecture is a melange composed of mudstone, sandstone and chert<br />
with a small amount of greenstones and limestone, ranging from<br />
Carboniferous to Jurassic in age. On the basis of the lithologic<br />
character, this complex is subdivided into four units, namely the Kl,<br />
K2, K3 and K4 in ascending order. Judging from the lithological,<br />
structural and chronological character, the Kanoashi Complex is<br />
regarded as an accretionary complex which was formed in a Jurassic<br />
subduction zone. Reconstructed strata of the Kanoashi Complex<br />
show that pelagic chert is always overlain by terrigenous clastic<br />
rocks. The youngest fossil age of the chert and the mudstone of<br />
each unit is younger than the unit above it. This younging direction<br />
from the upper unit to the lower one is explained by downward<br />
growing of the accretionary complex. This complex is correlated with<br />
the oldest unit of the Jurassic complex in the Mino and Tamba<br />
terrane, Southwest Japan.<br />
Furutani, H. 1990. Middle Paleozoic <strong>radiolaria</strong>ns from<br />
Fukuji Area, Gifu Prefecture, central Japan. J. Earth Sci.<br />
Nagoya Univ., 37, 1-56.<br />
Paleontological studies of middle Paleozoic <strong>radiolaria</strong>ns were<br />
carried out in the Fukuji Area, Gifu Prefecture, Central Japan.<br />
Paleozoic rocks of the Fukuji Area are divided into three facies: i.e.<br />
facies A, mainly composed of limestone and calcareous shale; facies<br />
B, mainly composed of clastic or pyroclastic rocks such as<br />
tuffaceous shale, tuff, sandstone and conglomerate; facies C,<br />
containing various kinds of rocks mainly pyroclastic and siliceous<br />
sedimentary rocks. Radiolarian fossils were extracted mainly from<br />
tuffaceous shale and shale of the facies B. In the <strong>radiolaria</strong>n fauna<br />
five assemblages are recognized: i.e. Fusalfanus osobudaniensis<br />
Assemblage, Spongocoelia parvus - Spongocoelia kamitakarensis<br />
Assemblage, Zadrappolus yoshikiensis Assemblage, Stylosphaera?<br />
sp. A - Stylosphaera? sp. B Assemblage, and Stylosphaera? sp. C<br />
Assemblage in ascending order. Fusalfanus osobudaniensis<br />
Assemblage, Wenlockian or early Ludlovian in age, is characterized<br />
by Fusalfanus osobudaniensis, Secuicollacta itoigawai, Secuicollacta<br />
typica, Goodbodium elegans. Spongocoelia parvus and Spongocoelia<br />
kamitakarensis Assemblage, late Ludlovian or Pridolian, is<br />
characterized by Spongocoelia parvus, Spongocoelia kamitakarensis,<br />
Zadrappolus spinosus, and Secuicollacta vulgaris. Zadrappolus<br />
yoshikiensis Assemblage, latest Silurian or early Devonian, is<br />
characterized by Zadrappolus yoshikiensis, Zadrappolus tenuis, and<br />
Futobari morishitai. Stylosphaera? sp. A - Stylosphaera? sp. B<br />
Assemblage, early or middle Devonian, is characterized by<br />
Stylosphaera? sp. A, Stylosphaera? sp. B, and some undetermined<br />
species of Zadrappolus and Futobari. Stylosphaera? sp. C<br />
Assemblage, middle Devonian, is characterized by Stylosphaera? sp.<br />
C. Any <strong>radiolaria</strong>ns are not obtained from the facies A. Poorly<br />
preserved <strong>radiolaria</strong>ns with middle Devonian aspect were obtained<br />
from the siliceous rock of the facies C. In the Early Devonian time<br />
the rocks of the facies A, B, and C were probably contemporaneous<br />
heterotopic facies. The facies A, B, and C are represented by the<br />
Fukuji Formation, the part of the Zadrappolus yoshikiensis<br />
Assemblage and Stylosphaera ? sp. A and S? sp. B Assemblage, and<br />
the rock which yields Spongocoelia sp., respectively. It is considered<br />
that in the Early Devonian time the three facies were deposited from<br />
the shore to open sea in the order of the facies A, B, to C. At least a<br />
- 47 -<br />
part of Devonian <strong>radiolaria</strong>ns are thought to be dwellers of the<br />
neritic sea. In the Late Silurian time the facies A and the facies B<br />
were thought to be under the same condition as the Early Devonian<br />
time. Within the middle Paleozoic spicule bearing <strong>radiolaria</strong>ns seven<br />
types of spicules are recognized. Such <strong>radiolaria</strong>ns should be<br />
classified based on the construction of the spicule.<br />
28 species belonging to 17 genera are described, of which 7<br />
genera and 21 species are new. The genus Futobari n. gen. is<br />
characterized by a single cortical shell, double medullary shell, and 5<br />
to 7 strong conical spines. The genus Zadrappolus n. gen. is<br />
characterized by a single cortical shell, double medullary shells, and<br />
numerous cylindrical spines. The genus Fusalfanus n. gen. is<br />
characterized by a spongy cortical shell with a pylome, double<br />
medullary shells, and many tapered spines. The genus Goodbodium n.<br />
gen. is characterized by having a tent-like shell and pendant spinules<br />
along the surface of the pyramid edged by four basal spines. The<br />
genus Holdsworthum n. gen. is characterized by a conical net formed<br />
by repeated bifurcations of three or four basal spines, and by the<br />
porous or poreless lamellae developed at the proximal part of the<br />
cone. The genus Fukujius n. gen. is characterized by 12 spines: i.e. 2<br />
apical, 6 lateral, and 4 basal spines. The genus Nazaromistonella is<br />
characterized by having an oval ring, an intersector penetrating the<br />
ring, and other three extra-ring spines.<br />
Garrison, D.L. & Gowing, M.M. 1990.<br />
Protozooplankton. In: Antarctic Microbiology. (Friedman,<br />
E.I., Eds.). Wiley-Liss, pp. 123-165.<br />
Gersonde, R. et al. 1990. Biostratigraphic synthesis of<br />
Neogene siliceous microfossils from the Antarctic Ocean,<br />
ODP Leg 113 (Weddell Sea). In: Proceedings of the Ocean<br />
Drilling Program, Scientific Results. (Barker, P.F., Kennett,<br />
J.P. et al., Eds.), vol. 113. College Station, TX (Ocean<br />
Drilling Program), pp. 915-936.<br />
This paper summarizes the magnetostratigraphic and<br />
biostratigraphic results obtained with siliceous microfossils<br />
(diatoms, <strong>radiolaria</strong>ns, silicoflagellates) on Neogene sections<br />
recovered in the Weddell Sea (Antarctic Ocean) during Ocean Drilling<br />
Program Leg 113 (Sites 689, 690, 693, 694, 695, 696, and 697).<br />
The biostratigraphic studies resulted in the establishment of an<br />
improved and revised Neogene biosiliceous zonation for the<br />
Antarctic Ocean. The zones are calibrated directly to the<br />
geomagnetic time scale. This is the first attempt at direct<br />
calibration of Miocene Antarctic biostratigraphic zones with the<br />
geomagnetic time scale.<br />
Gorican, S. & Buser, S. 1990. Middle Triassic<br />
<strong>radiolaria</strong>ns from Slovenia (Yugoslavia). Geologija, 31-32,<br />
133-197.<br />
The <strong>radiolaria</strong>n fauna presented derives from five Middle<br />
Triassic localities in NW and central Slovenia. The sections consist<br />
of tuff and tuffite alternating with micritic limestone with chert. On<br />
the basis of <strong>radiolaria</strong>ns extracted from the limestone beds, an<br />
Upper Illyrian-Fassanian age is assumed for the Zaklanec, Bohinj and<br />
Vojsko localities and a Langobardian age for Vrsic and Mokronog. 89<br />
species are included in the investigation, four of them are newly<br />
described: Dumitricasphaera ? pennata, Falcispongus uncus,<br />
Hozmadia pyramidalis, Plafkerium ? firmum.<br />
Granlund, A. 1990. Evolutionary trends of Antarctissa in<br />
the Quaternary using morphometric analysis. Mar.<br />
Micropaleontol., 15/3-4, 265-286.<br />
Three piston cores from a latitudinal traverse across the Polar<br />
Front in the southeast Indian Ocean have been used as the basis for<br />
a morphological analysis of the Antarctissa complex (Radiolaria) . All<br />
three cores penetrate sediments deposited during at least the last<br />
0.5 Ma B.P. The <strong>radiolaria</strong>n genus Antarctissa has been selected to<br />
look for variations in size and shape through time. The method used<br />
is an interactive outline detection utilizing a cubic b-spline<br />
technique. Shape change is evaluated by phi function analysis. Size<br />
variability is measured by the area of the test. The results of this<br />
study indicate that Antarctissa tests seem to oscillate in size and<br />
shape according to prevailing oceanographical/climatological<br />
conditions, and thus they may be employed as indices of<br />
paleoclimatological fluctuations in the Southern Ocean. The size<br />
pattern for Antarctissa shows larger forms during glacial periods<br />
and smaller forms during interglacial periods. For the shape change,<br />
the study is differentiated between an allometric component and one<br />
growth-free component. The allometric component shows variation<br />
closely related to the size pattern, i.e. an oscillating pattern close to<br />
the changes in glacial interglacial patterns. The growth-free shape<br />
component on the other hand shows a long-term variation in shape<br />
that may be interpreted as change due to evolution. The use of the<br />
computerized measuring technique employed here, enables
Bibliography - 1990 Radiolaria 14<br />
measurements of a large number of specimens per sample and<br />
provides information of use in obtaining a high-resolution<br />
stratigraphy.<br />
Grapes, R.H., Lamb, S.H., Campbell, H.J.,<br />
Spörli, B. & Simes, J.E. 1990. Geology of the red<br />
rocks - turbidite association, wellington peninsula, New<br />
Zealand. New Zealand J. Geol. Geophys., 33/2, 377-391.<br />
Two models are proposed to explained the red rocks greywacke<br />
turbidite association: I) the red rocks are the top part of Late<br />
Permian oceanic crust overlain by Late Triassic turbidites that was<br />
sheared off by decollement and incorporated into an accretionary<br />
prism of a Late Triassic subduction zone; 2) the red rocks are<br />
submarine gravity slides of "oceanic" material from Late Permian<br />
seamounts as they encroached upon an area of Late Triassic<br />
turbidite deposition.<br />
Gursky, H.J. 1990. Radiolarian petrographic preservation<br />
types in Jurassic to Lower Tertiary cherts of Costa Rica. Mar.<br />
Micropaleontol., 15/3-4, 249-263.<br />
Radiolarian cherts are locally intercalated, mostly as up to 45<br />
m thick sequences of rhythmically bedded chert, in the Jurassic to<br />
Lower Tertiary Nicoya Ophiolite Complex of western and southern<br />
Costa Rica (Central America). Additionally, bedded chert is present<br />
in some Campanian and Paleocene/Eocene sedimentary series that<br />
overly the Nicoya Complex. The ophiolitic cherts may be thermally<br />
recrystallized to different grades due to post depositional basaltic<br />
magmatism. The <strong>radiolaria</strong>n skeletons mainly consist of microquartz;<br />
complete dissolution of the skeletons, i.e. exclusive preservation of<br />
the fillings, is rare. The fillings are variable in composition: quartz,<br />
length-fast chalcedony, and quartz-pigment mixtures are dominant;<br />
opal-CT, clay minerals, chlorite, zeolites, baryte, manganese and iron<br />
oxides, epidote and calcite are subordinate. The non-siliceous<br />
minerals may locally replace the siliceous phases and/or intergrow<br />
with them. Thus, approximately 40 preservation types have been<br />
observed in the Costa Rican cherts.<br />
In combination with the different preservation grades, a large<br />
number of preservation variants is present. However, in the cherts<br />
of the Nicoya Complex quartz-rich preservation types are strongly<br />
dominant, whereas opal-CT, zeolites and calcite are more important<br />
in the cherts of the overlying sedimentary series. Types and grades<br />
of <strong>radiolaria</strong>n preservation represent an important aid in the<br />
reconstruction of the postdepositional diagenetic and thermal<br />
history of the Costa Rican cherts.<br />
Hagelberg, T.K. & Pisias, N. 1990. Nonlinear<br />
response of Pliocene climate to orbital forcing: evidence<br />
from the eastern equatorial Pacific. Paleoceanography, 5/4,<br />
595-617.<br />
A high-resolution <strong>radiolaria</strong>n record from the eastern Equatorial<br />
Pacific is used to examine Paleoceanographic events during the<br />
Pliocene, from 1.8 to 1.9 Ma. These data provide a means to<br />
evaluate the response of the equatorial Pacific to the onset of<br />
northern hemisphere glaciation near 12.47 Ma and to the closure of<br />
the Isthmus of Panama near ~3.2 Ma. Responses are recorded both<br />
as long-term trends and as variations within the Milankovitch band<br />
(104 to 105 years). Radiolarian-based sea surface temperature<br />
(SST) estimates indicate a mean cooling from lower to upper<br />
Pliocene, but no significant changes occur near the onset of northern<br />
hemisphere glaciation, and no abrupt changes are observed before or<br />
after the closure of the isthmus. Time series analysis of the SST and<br />
∂ 18 O time series indicates a strongly nonlinear relationship<br />
between Pliocene climatic variables and Earth's orbit. A strongly<br />
nonlinear response of equatorial Pacific SST and planktonic ∂ 18 O to<br />
orbital forcing in the Pliocene is suggested. Although the reasons for<br />
this response are still unclear, it is evident that strong nonlinearities<br />
in climate are present during this time.<br />
Harwood, D.S. & Murchey, B.L. 1990.<br />
Biostratigraphic, tectonic, and paleogeographic ties between<br />
upper Paleozoic volcanic and basinal rocks in the northern<br />
Sierra Terrane, California, and the Havallah Sequence,<br />
Nevada. In: Paleozoic and early Mesozoic paleogeographic<br />
relations; Sierra Nevada, Klamath Mountains, and related<br />
terranes. (Harwood, D.S. et al., Eds.), vol. 255. Geological<br />
Society of America, special Papers, pp. 157-173.<br />
Biostratigraphic data, based mostly on <strong>radiolaria</strong>n assemblages,<br />
establish synchronous deposition in the northern Sierra terrane and<br />
the Havallah basin beginning in the Late Devonian and extending into<br />
the early Late Permian. Lower Mississippian and mid-Permian arcderived<br />
volcaniclastic debris was deposited in parts of the Havallah<br />
basin during episodes of arc volcanism in the northern Sierra<br />
terrane. Between these episodes of arc volcanism, from late Early<br />
- 48 -<br />
Mississippian to at least Middle Pennsylvanian, the northern Sierra<br />
terrane collected siliceous pelagic deposits that correlate with<br />
dominantly chert-argillite sections in the Havallah sequence. These<br />
intermixed lithic assemblages suggest shared stratigraphic<br />
evolution and geographic proximity between the Sierran arc terrane<br />
and the Havllah basin during the late Paleozoic. During Late Devonian<br />
and Early Mississippian arc volcanism in the northern Sierra terrane,<br />
lower Paleozoic rocks of the Roberts Mountains allochthon were<br />
thrust over coeval deposits on the North American shelf. Chertquartz-rich<br />
siliciclastic debris, derived from the Antler orogenic belt,<br />
is interbedded with Upper Devonian and Lower Mississippian distal<br />
volcanic rocks in the northern Sierra terrane and with Kinderhookian<br />
volcaniclastic rocks and chert in the Schoonover sequence. These<br />
quartzose-clastic deposits not only provide an independent lithologic<br />
link between the Sierran arc terrane and the Havallah basin, they<br />
also tie the arc terrane and basin to North America at the time of the<br />
Antler orogeny. Late Devonian and Early Mississippian arc volcanism<br />
in the northern Sierra terrane occurred in an extensional regime.<br />
Extensional tectonism began locally in the Havallah basin during the<br />
Famennian and continued into the early Meramecian.<br />
Contemporaneous extension in the arc and basin during<br />
emplacement of the Roberts Mountains allochthon is difficult to<br />
reconcile with existing arc-continent collision models for the Antler<br />
orogeny.<br />
Helmcke, J.G. & Bach, K. 1990. Radiolaria in<br />
stereoscopic micrographs. Processe of form generation. In:<br />
Shells in stereoscopic micrographs. (Otto, F., Eds.), vol.<br />
33. Mitteilungen des Institut für Leichte Flächentragwerke<br />
(IL), Universität Stuttgart, Stuttgart. pp. 313.<br />
In this volume 33 of our IL series I have the pleasure as editor<br />
to present two works which complement each other although they<br />
were written at different times. We have at last been able to print<br />
the article "Radiolaria in Stereoscopic nicrographs" by J.-G.<br />
HELMCKE, following earlier publication of individual stereoscopic<br />
pairs of photographs in the form of transparencies in stereoscopic<br />
projection. For a long time we thought that the originals had been<br />
lost until they were luckily found again. Klaus BACH's study entitled<br />
"Processes of Form Generation" on Radiolaria was a logical sequel<br />
following the study of a similar theme in respect of diatoms (see IL<br />
28 Diatoms I). There are, however, a number of differences between<br />
Radiolaria and diatoms which make Radiolaria more interesting with<br />
regard to the generation of their forms. At the same time<br />
considerable problems are encountered. whereas diatoms can be<br />
found in nearly any puddle, living Radiolaria must be caught in the<br />
oceans. The catches are quite random. We have not yet found out<br />
whether Radiolaria embrace a large number of species or whether the<br />
forms we have found are merely variations of a few basic forms.<br />
IL is a centre for architects. It is not the architect's task to<br />
formulate statements belonging to the realm of biology.<br />
Consequently Klaus BACH limits himself to the aspects of shape,<br />
structure, texture and material and to making comparisons with<br />
similar objects and optimising methods in engineering, especially in<br />
building construction, by using appropriate illustrations. He includes<br />
the central area of study of "Lightweight Structures", in which IL<br />
specialities, and the Special Research Project 230 entitled 'Natural<br />
Constructions'. The emphasis is placed on self-generation and selfoptimisation.<br />
Working groups researching into the forms and<br />
structures of living objects have participated in this work.<br />
It should be emphasised that it was not the author's intention to<br />
establish whether the structure of Radiolaria could serve as a<br />
pattern for human engineering and technology, especially with regard<br />
to lightweight roofs, building shells or walls. In this respect<br />
Radiolaria are not particularly useful, although, like almost all<br />
objects of living nature, they may be regarded at highly optimised<br />
lightweight structures.<br />
Given the present relatively advanced state of knowledge of<br />
lightweight building construction, we cannot really expect living<br />
nature to furnish us with examples of such optimised structures. It<br />
may, however, be quite possible to utilise our knowledge of<br />
lightweight building construction to analyse the forms found in<br />
nature very accurately and possibly to understand them somewhat<br />
better than hitherto. This is precisely the theme of this study and a<br />
fascinating task which encompasses architecture, building<br />
construction and biology.<br />
Klaus BACH's study is based on illustrated documentation. To<br />
begin with, there are the unsurpassed plates by HAECKEL. In addition<br />
J.-G. HELMCKE's entire archive of illustrations and photographs was<br />
made available to him. A selection of these photographs, which were<br />
taken in the Fifties and Sixties using a highly advanced method of<br />
stereoscopic electron microscopy is reproduced in the illustration<br />
section. By using the enclosed stereoscopic viewer, the spectator<br />
can experience the spatial depths of these microscopic skeletons.<br />
Further materials used are photographs by O. Roger ANDERSON, New<br />
York, and very recent films of living Radiolaria taken by Manfred<br />
KAGE, Weisenstein.
Radiolaria 14 Bibliography - 1990<br />
That applies to many aspects of life equally applies to<br />
architecture: although a building may be planned as perfectly as<br />
humanly possible, it will always feature a certain degree of selforganisation,<br />
self-generation and self-formation which cannot be<br />
prevented by the planners. This starts with the initial design sketch,<br />
continues through the building phase and ends in the utilisation of<br />
the building. The concept that a building can be totally planned is<br />
nowadays regarded as an unrealistic ideal.<br />
A different train of thought is, however, gaining in importance:<br />
if processes of self-generation and self-organisation are<br />
unavoidable, the designing architect should at least recognise and<br />
exploit them, if possible. Processes of self-generation, be it physical<br />
processes or the actions of the users of a building, may well produce<br />
better solutions than an individual designer/planner. The degree of<br />
self-generation and also of accidence can vary greatly in<br />
architecture and town planning. On the one hand we find completely<br />
unplanned self-forming networks of paths in spontaneously formed<br />
structures of settlements, while on the other hand we have the<br />
'perfectly' designed headquarters of a bank in which nothing is left<br />
to self-organisation or chance.<br />
Those experiments which began after the war and were in<br />
principle of a physical nature, should be regarded as part of the<br />
research into processes of self-generation. These experiments were<br />
looking for effective for-s for vaults, grid shells, cable and<br />
membrane structures such as tents and airhouses (pneumatics) by<br />
using chains, rubber threads, coil springs, soap film models as well<br />
as tulle fabric models. In 1961 the biologist HELMCKE pointed out to<br />
his fellow researchers and especially to architects that in biology<br />
processes of self-generation appear -in conjunction with genetically<br />
controlled reproduction- to play a part which cannot be ignored. He<br />
attempted to furnish proof of this theory by using the bubbly/foamy<br />
structures of diatom shells whose particular arrangement can<br />
evidently be explained only by self-organisation. He discovered that<br />
new findings in the fields of architecture (i.e.. lightweight building<br />
construction) and aeroplane construction could be used to explain<br />
this type of self-organisation.<br />
It was in fact the experimental results gained from the minimal<br />
surfaces of soap films and the experience gained with a number of<br />
buildings based on these experiments, which planed the way for the<br />
interpretation of forms, structures and textures found in living<br />
natures. It was mainly the processes of self-organisation of liquid<br />
droplets, bubbles and films which had to be applied to other fields. It<br />
was furthermore observed that fibre structures can form inside<br />
bubbles and that these structures are capable of hardening either by<br />
bonding of the fibres or by forming hard substances. It was also<br />
found that a different process of self-generation found in inanimate<br />
nature, i.e.. that of crystallisation, applies only rarely to living nature<br />
where it appears to disturb the production process of living<br />
organisms because the structural forms of the crystals<br />
fundamentally differ from that of bubbles and membranes. For this<br />
reason the siliceous skeletons of diatoms and Radiolaria are not<br />
crystalline but rather comparable to amorphous quartz or window<br />
glass with similar strength characteristics, although they are not the<br />
product of a hot melting process but rather the result of a cold<br />
process which we have been unable to emulate so far.<br />
HELMCKE's theory of the effect of self-generation not<br />
controlled by genetics, which was largely influenced by the study of<br />
HAECKEL's drawings and the publications by D'Arcy W. THOMPSON,<br />
proved very instructive to those familiar with membrane and net<br />
structures, tents, pneumatics and airhouses, and multibated their<br />
researches in which Klaus BACH participated intensively.<br />
It was shown that an infinitely large number forms can be<br />
explained by processes of selfgeneration which occur abiotically. To<br />
start with there is the self-organisation of bubbles in various<br />
numbers, sizes and internal pressures. If fibre structures are added<br />
to this and if these fibres are allowed to bond to each other or to be<br />
made rigid by hardening substances, any biological form can be<br />
explained. The result cannot be -and never has been- to declare our<br />
knowledge of genetically based production and reproduction and of<br />
the growth of organisms to be invalid. This knowledge is simply<br />
extended by the knowledge of abiotic processes of self-generation.<br />
It should be noted in passing that there are still biologists, even<br />
amongst <strong>radiolaria</strong>n researchers, who are not familiar with the full<br />
extent of the abiotic processes of self-generation in question -partly<br />
because these findings have been published only recently- and who<br />
continue to adhere to the opinion that the forms of the organisms<br />
and particularly the distinguishing features of the species are either<br />
exclusively or largely genetically predetermined and who regard the<br />
formation of Radiolaria as unequivocally genetically coded.<br />
In all the studies of the past years on which, among others,<br />
Klaus BACH reports in his dissertation, two questions have been of<br />
interest within IL and the Special Research Project 230:<br />
1. If a large number of forms, structures and natural objects<br />
can also be generated abiotically, where does genetic planning start<br />
without which the generation of species and the phenomenon of<br />
- 49 -<br />
inheritance cannot be explained? The initially hypothetical answer to<br />
this question was quickly found for the 'soft' organisms: If there are<br />
no hard components and the organisms consist only of closed soft<br />
vessels (pneumatics), the abiotically generated bubble forms are not<br />
sufficient to explain more complex organisms and one has to add the<br />
linking mechanisms of the fibrous nets in the membrane or the<br />
interior of the pneumatic as well as the processes of change and<br />
growth caused by the varying internal pressure. It is only at this<br />
point that the shape can be determined, and<br />
2. How did the skeletons consisting of hard substances form?<br />
In this area again there are only some ideas which may be regarded<br />
as a preliminary answer. There are still some insurmountable<br />
problems. The form-generating fibre skeletons of the soft organisms<br />
can be very fine and may consist only of elongated large molecules<br />
which are two-dimensionally or three-dimensionally linked and have<br />
an adequate tensile strength. Such molecules have not been fount<br />
to-date even by the use of electron microscopes. They can be<br />
recognised only by means of their effect on the shape of the objects.<br />
They can, however, be detected if they occur in the form of bundles.<br />
Such bundles have been verificated in large numbers (e.g.<br />
cytoskeletons).<br />
If the production of Radiolaria with hard skeletons initially<br />
requires a soft 'youth form' -such a form could hardly be caught or<br />
observed since it almost entirely consists of water the following<br />
strong suspicion emerges: the hard skeleton is merely the hardened<br />
bubble or the fibre net formed by the bubble which develops into a<br />
hard skeleton by the ingress of siliceous substance which<br />
subsequently hardens. From this we conclude that the "soft young<br />
skeleton" consisting of bubbles and fibres, is tensioned by the<br />
internal pressure. It can expand and grow. The subsequent hardening<br />
'freezes' the expanded or tensioned status. ~e also believe that the<br />
hardening of the siliceous mass in the cold state can be possible<br />
only in the presence of organic fibres. If the theory is correct -which<br />
ought to be assumed, not least because of the author's study the<br />
siliceous skeleton of Radiolaria (and diatoms) is identical to the soft<br />
'young' skeleton under tensile stress which cannot be observed. As<br />
shown by the more recent light microscopic images produced by<br />
KAGE's, the hard skeleton appears to be only a part of this young<br />
skeleton and is most frequently found in the interior of the living<br />
<strong>radiolaria</strong>n cell.<br />
What are the functions of the hard skeletons? So far we have<br />
not found any conclusive evidence. Perhaps the skeleton provides<br />
protection against predators making the Radiolaria unpalatable and<br />
not easily digestible. It should, however, be noted that the hard<br />
skeleton allows the internal pressure in the cell to be lowered and<br />
even to become negative, at least for a short period. KAGE's films on<br />
acantharia seem to suggest this. The partial vacuum may facilitate<br />
the ingestion of food and water. I hope that the book produced by the<br />
two authors will provide a basis for many discussions between<br />
architects, engineers and biologists, which will continue the theme of<br />
"form-generating processes".<br />
Hori, R. 1990. Lower Jurassic Radiolarian Zones of SW<br />
Japan. Trans. Proc. palaeont. Soc. Japan, n. Ser., 159, 562-<br />
586.<br />
Four Lower Jurassic <strong>radiolaria</strong>n assemblage-zones and four<br />
subzones are established on the basis of <strong>radiolaria</strong>n biostratigraphic<br />
data from the Inuyama and three other areas of SW Japan. These<br />
zones are as follows in ascending order: the Parahsuum simplum<br />
(divided into Subzone I to IV), Mesosaturnalis hexagonus (newly<br />
proposed), Parahsuum (?) grande and Hsuum hisuikyoense<br />
Assemblage-zones. These zones range in age from latest<br />
Triassic/earliest Jurassic (Rhaetian/Hettangian ?) to early Middle<br />
Jurassic (Bajocian). This age assignment is based on comparison<br />
with Early to Middle Jurassic <strong>radiolaria</strong>n biostratigraphy established<br />
in North America and Turkey.<br />
Ishiga, H. 1990a. Paleozoic <strong>radiolaria</strong>ns. In: Pre-<br />
Cretaceous Terranes of Japan. Publication of IGCP Project<br />
No. 224: Pre-Jurassic Evolution of Eastern Asia. (Ichikawa,<br />
K., Mizutani, S., Hara, I., Hada, S. & Yao, A., Eds.). IGCP<br />
Project 224, Osaka, Japan. pp. 285-295.<br />
Study of Paleozoic <strong>radiolaria</strong>ns, especially, late Carboniferous<br />
through Permian <strong>radiolaria</strong>n biostratigraphy of Japan has been much<br />
improved during these several years (see Ishiga, 1986b). However,<br />
reports on Middle to Early Paleozoic <strong>radiolaria</strong>ns have been less<br />
common in Japan, for rocks of those ages are restricted to narrow<br />
tectonic belts. This paper summarizes the recent results on the<br />
examination of Middle to Late Paleozoic <strong>radiolaria</strong>n biostratigraphy<br />
and provinciality of Late Permian <strong>radiolaria</strong>n assemblages in<br />
Southwest Japan.<br />
Ishiga, H. 1990b. Radiolarians from the Gympie Province,<br />
eastern Australia. In: Proceeding of the Pacific Rim Congres<br />
1990. Eds.), vol. 3. Aust. Inst. Min. Metal., pp. 187-189.
Bibliography - 1990 Radiolaria 14<br />
Ishiga, H., Choi, J. & Sato, M. 1990. Geologic<br />
examination of the borehole data from the eastern part of the<br />
Himeji Prefecture, Southwest Japan. Geol. Rep. Shimane<br />
Univ., 8, 61-71. (in Japanese)<br />
Geologic structure and stratigraphy of the Permo-Triassic<br />
strata of the Kozuki-Tatsuno Belt in the eastern part of the Himeji<br />
area. Southwest Japan were examined on the basis of the borehole<br />
data which has 1440m depth from the ground. The rock unit in this<br />
area consists of the Permian Tatsuno Group and the unnamed<br />
Triassic strata, and they are repeated by thrust fault. Mudstones of<br />
the Tatsuno Group from the horizon 735m of the borehole yield<br />
Pseudoalbaillella aidensis, P. yanaharensis, P. globosa and P. spp.<br />
Sandstones of the Tatsuno Group are characterised by wacke<br />
including plagioclase, rock fragments and less amount of quartz<br />
grains, while sandstones of the Triassic formation is arenite.<br />
characterised by large amound of quartz, K-feldspar and less<br />
amount of rock fragments.<br />
Although the Triassic formation is not distributed on the ground<br />
surface, the borehole data reveals that the strata correlative to the<br />
Hiraki Formation is widely distributed in the Kozuki-Tatsuno Belt. The<br />
granitic rocks appears just beside to the east of the examined area,<br />
and this granites occurs in the 1200m depth. Thus, the fault with<br />
NE-SW direction cut the strata and the block of the ground greatly<br />
upheaved about 900m judging from the difference of the horizons of<br />
contact between granitic intrusion and the sediments in each block.<br />
Ishii, A., Takahashi, O. & Hayashi, N. 1990.<br />
Geology of the Kawakami-Sudama area, western part of the<br />
Kanto Mountains, central Japan. Bull. Tokyo Gakugei Univ.<br />
Sect. 4, 42, 171-181. (in Japanese)<br />
Iwata, K., Hariya, Y., Choi, J.H., Yagi, E. &<br />
Miura, T. 1990. Radiolarian age of the manganese deposits<br />
of the tokoro belt, northeast Hokkaido. J. Fac. Sci. Hokkaido<br />
Univ., 22/4, 565-576.<br />
Radiolarian fossils of early Cretaceous (middle Barremian-early<br />
Aptian) were obtained from the country rock (bedded red chert) of<br />
the manganese deposit of the Hinode mine in the Tokoro Belt. By this<br />
discovery of <strong>radiolaria</strong>ns the geological age of the formation of the<br />
manganese deposit of the Hinode mine was determined for the first<br />
time to be formed during a short period of ca. 110-120 Ma.<br />
Radiolarian fossils of early Cretaceous in age were also extracted<br />
from bedded cherts of the Wakasa, Koryu, Syotosibetu, and<br />
Hokkaido mines which were similar manganese deposits to the<br />
Hinode mine. This fact suggests that manganese deposits in the<br />
Tokoro Belt were formed almost simultaneously during late early<br />
Cretaceous time.<br />
Jauhari, P. 1990. Relationship between morphology and<br />
composition of manganese nodules from the central Indian<br />
Ocean. Marine Geol., 92/1-2, 115-125.<br />
Spheroidal nodules having a diameter between 2 and 4 cm and<br />
surface textures ranging from smooth to coarsely granular or of<br />
intermediate nature are the most common. The nodule facies and<br />
their compositions are influenced by the underlying sediment<br />
through which they receive some of their constituents. The<br />
association of coarse texture with the siliceous sediments reflects<br />
the precipitation of larger particles of manganese oxides through the<br />
larger pore spaces of the sediment as a result of the enhanced early<br />
diagenetic effects. The smooth texture, in contrast, reflects the<br />
direct supply of manganese oxides from the overlying bottom water<br />
as a result of their precipitation as authigenic oxyhydroxides.<br />
Johnson, D.A. 1990. Radiolarian biostratigraphy in the<br />
central Indian Ocean, Leg 115. In: Proceedings of the Ocean<br />
Drilling Program, Scientific Results. (Duncan, R.A.,<br />
Backman, J., Peterson, L.C. et al., Eds.), vol. 115. College<br />
Station, TX (Ocean Drilling Program), pp. 395-409.<br />
Identifiable <strong>radiolaria</strong>ns of stratigraphic importance were<br />
recovered at eight of the sites drilled on Leg 115. The assemblages<br />
range in age from Holocene to middle Eocene (Dictyoprora<br />
mongolfieri Zone, about 48 Ma). Faunal preservation is particularly<br />
good in two stratigraphic intervals: the Holocene through upper<br />
Miocene (0-9 Ma), and the lowermost Oligocene to middle Eocene<br />
(35-48 Ma). Fluctuating rates of silica accumulation at these drill<br />
sites during the Cenozoic reflect changing tectonic and<br />
paleoceanographic conditions. In particular, the gradual closure of<br />
the Indonesian and Tethyan seaways and the northward migration of<br />
the Indian subcontinent severely restricted zonal circulation and<br />
silica accumulation in tropical latitudes during the late Oligocene<br />
through middle Miocene. By the late Miocene the Indian subcontinent<br />
had moved sufficiently north of the equator to allow trans-Indian<br />
zonal circulation patterns to become re-established, and biosiliceous<br />
- 50 -<br />
sedimentation resumed. The composition of the <strong>radiolaria</strong>n<br />
assemblages in the tropical Indian Ocean is closely comparable with<br />
that of the "stratotype" sequences in the equatorial Pacific.<br />
However, there are some notable exceptions in Indian Ocean<br />
assemblages: (I) the scarcity of the genera Pterocanium and<br />
Spongaster in the Neogene; (2) the absence of the stratigraphically<br />
important Podocyrtis lineage, P. diamesa ⇒ P. phyxis ⇒ P. ampla, in<br />
the middle Eocene; and (3) the scarcity of taxa of the genus<br />
Dorcadospyris, with the exception of D. ateuchus. The succession of<br />
<strong>radiolaria</strong>n events was tabulated for those stratigraphic intervals<br />
where the assemblages were well preserved. We identified 55<br />
events in the middle Eocene to earliest Oligocene and 31 events in<br />
the late Miocene to Holocene. The succession of events is closely<br />
comparable with that of the tropical Pacific. However, there are<br />
exceptions that appear to be real, rather than artifacts of sample<br />
preservation, mixing, and core disturbance.<br />
Khokhlova, I.Y. 1990. The Neogene stratigraphy of the<br />
temperate and south-borealic Pacific Radiolaria. Izv. Akad.<br />
Nauk SSSR, ser. geol., 1, 18-28. (in Russian)<br />
Neogene deposits, discovered in the northern part of the Pacific<br />
ocean by wells 578, 580 and 581 of the DSDP, were divided in<br />
accordance with the zonal scale on the basis of <strong>radiolaria</strong>, and<br />
correlated. The zonal complexes of <strong>radiolaria</strong> from the temperate<br />
and southern boreal N zones of the Pacific ocean were described.<br />
They were compared with each other and with coeval tropical<br />
complexes. The zones based on Radiolaria were compared with<br />
palaeomagnetic data about the same wells. The positions of the<br />
boundaries of identical zones in the tropics and the temperate zone<br />
were found to be different.<br />
Kiminami, K., Kawabata, K. & Miyashita, S.<br />
1990. Discovery of Paleogene <strong>radiolaria</strong>ns from the Hidaka<br />
Supergroup and its significance with special reference to ridge<br />
subduction. J. geol. Soc. Japan, 96/4, 323-326. (in<br />
Japanese)<br />
The Mesozoic rocks of the Hidaka Belt distributed on the<br />
central part of Hokkaido, Japan are made up the Hidaka Supergroup.<br />
The Hidaka Supergroup is composed mainly of turbidite and melange,<br />
and is considered to be accretionary body formed by west ward<br />
subduction of Cretaceous in time. The accretionary body are divided<br />
into two parts, they are western margin area and eastern area by<br />
<strong>radiolaria</strong>n fossils. The former is early Cretaceous and latter is<br />
considered to be late Cretaceous, approximately Campanian in age.<br />
The westward subduction formed the Hidaka Belt are also thought to<br />
be finished till late Cretaceous on the basis of these <strong>radiolaria</strong>n<br />
ages. In this paper, we reported the discovery of Paleogene (approx.<br />
middle to late Eocene) <strong>radiolaria</strong>n fossils from the eastern margin of<br />
the Hidaka Belt and discussed its significance.<br />
Kito, N. & De Wever, P. 1990. Analyse cladistique de la<br />
phylogenie des Hagiastridae (Radiolaires Mésozoïques). Rev.<br />
Micropaléont., 33/3-4, 193-218.<br />
An analysis of the relationships of the Hagiastridae has been<br />
undertaken with the parcimony method in order to compare these<br />
results with previous propositions. The study has been carried out<br />
with 16 characters. 19 taxa are clustered within two subfamilies:<br />
Archaeohagiastrinae and Hagiastrinae, the later being subdivided<br />
into three tribes. The resulting phylogenetic tree situated in its<br />
stratigraphic frame, reveals two main periods of diversification: one<br />
during the Hettangian and one about the Toarcian.<br />
Kito, N., De Wever, P., Danelian, T. & Cordey,<br />
F. 1990. Middle to Late Jurassic <strong>radiolaria</strong>ns from Sicily<br />
(Italy). Mar. Micropaleontol., 15/3-4, 329-349.<br />
Middle and Upper Jurassic <strong>radiolaria</strong>n faunas from two sections<br />
of Sicily are compared with the previously proposed zonations. The<br />
ages of the faunas are estimated by correlation with these zonations<br />
and by concurrent range zone. The faunas could be assigned to the<br />
Bathonian or earlier late Tithonian or early Berriasian. Two new<br />
spumellarian species (Bernoullius furcospinus and Bernoullius<br />
rectispinus) from Middle Jurassic are described.<br />
Koutsoukos, E.A.M. & Hart, M.B. 1990.<br />
Radiolarians and Diatoms from the mid-Cretaceous<br />
successions of the Sergipe Basin, northesatern Brazil:<br />
palaeoceanographic assessment. J. Micropaleont., 9/1, 45-<br />
64.<br />
Radiolarians and diatoms are documented for the first time<br />
from the mid- Cretaceous succession of the Sergipe Basin, a passive<br />
marginal basin in northeastern Brazil. Prevailing palaeoceanographic<br />
conditions are inferred for the episodes of siliceous <strong>radiolaria</strong>n and<br />
diatom biomineralization/preservation. Radiolarian faunas are first
Radiolaria 14 Bibliography - 1990<br />
recorded in the middle to upper Albian, from scattered occurrences<br />
,and subsequently throughout most of the Cenomanian-Turonian<br />
succession. Spumellarian forms are dominant in all the sections.<br />
Nassellarian forms seem to have thrived in relatively deep-water<br />
environments, in middle neritic to upper bathyal pelagic biotopes,<br />
and have been recovered from upper Albian and uppermost<br />
Cenomanian to middle Turonian sediments. Diatom frustules are only<br />
recorded from upper Cenomanian and lower Turonian deposits. These<br />
seem to have been more abundant in shallower neritic environments.<br />
The onset of the <strong>radiolaria</strong>n assemblages in middle-late Albian times<br />
(with waning low-oxygen pelagic conditions) is thought to be a<br />
response to better developed oceanic circulation pasterns and to a<br />
water mass saturated in dissolved silica, perhaps generated by<br />
deep-sea volcanic processes in the formation of early oceanic crust<br />
and the mid-oceanic ridge in the northern South Atlantic. On the<br />
other hand, the record of <strong>radiolaria</strong>n and diatom tests throughout the<br />
Cenomanian-Turonian succession is commonly associated with<br />
dysaerobic to quasi-anaerobic bottom conditions. This is not only in<br />
keeping with high epipelagic primary productivity in well-oxygenated<br />
surface waters and that the sea water apparently contained a high<br />
level of dissolved silica, but also suggests that the bottom and<br />
interstitial waters were enriched in carbon dioxide, had a low pH and<br />
slightly negative redox-potential (Eh). The overall conditions would<br />
have favoured the biomineralization and post-mortem preservation<br />
of siliceous organisms increasing, therefore, the <strong>radiolaria</strong>+diatom<br />
/foraminifera ratio in the sediments, which supports the conclusions<br />
of several previous authors.<br />
Kozur, H. & Mostler, H. 1990. Saturnaliacea Deflandre<br />
and some other stratigraphically important <strong>radiolaria</strong> from<br />
the Hettangian of Lenggries/Isar (Bavaria, Northern<br />
Calcareous Alps). Geol. Pälont. Mitt. Innsbruck, 17, 179-<br />
248.<br />
In the Kirchstein Limestone of the type locality 6.5 km WSW of<br />
Lenggries/Isar (Bavaria) rich <strong>radiolaria</strong>n and sponge spicule<br />
associations have been discovered about 1 m above the Rhaetian<br />
Dachstein Limestone. The <strong>radiolaria</strong>ns indicate Hettangian age. All<br />
discovered species of the Saturnaliacea DEFLANDRE, 1953 have<br />
been described. Additionally, the stratigraphically important species<br />
of other <strong>radiolaria</strong>n families have been described. 2 families, 7<br />
genera and 63 species have been newly established.<br />
Lazarus, D. 1990. Middle Miocene to Recent <strong>radiolaria</strong>ns<br />
from the Weddell Sea, Antarctica, ODP leg 113. In:<br />
Proceedings of the Ocean Drilling Program, Scientific<br />
Results. (Barker, P.F., Kennett, J.P. et al., Eds.), vol. 113.<br />
College Station, TX (Ocean Drilling Program), pp. 709-727.<br />
Well preserved middle Miocene to Recent <strong>radiolaria</strong>ns were<br />
recovered from several sites in the Weddell Sea by ODP(Ocean<br />
Drilling Program) Leg 113. Low rates of sedimentation, hiatuses, and<br />
poor core recovery in some sites are offset by the nearly complete<br />
recovery of a late middle Miocene to late Pliocene section at Site<br />
689 on the Maud Rise. Although a hiatus within the latest Miocene<br />
exists, this site still provides an excellent reference section for<br />
Antarctic biostratigraphy. A detailed <strong>radiolaria</strong>n stratigraphy for the<br />
middle Miocene to late Pliocene of Site 689 is given, together with<br />
supplemental stratigraphic data from ODP Leg 113 Sites 690, 693,<br />
695, 696, and 697. A refined Antarctic zonation for the middle<br />
Miocene to Recent is presented, based on the previous zonations of<br />
Hays (1965), Chen (1975), Weaver(1976b), and Keany (1979).<br />
The late Miocene <strong>radiolaria</strong>n Acrosphaera australis n. sp. is<br />
described and used to define the A. australis zone, ranging from the<br />
first appearance of the nominate species to the last appearance of<br />
Cycladophora spongothorax (Chen) Lombari and Lazarus 1988. The<br />
species Botryopera deflandrei Petrushevskaya 1975 is transferred<br />
to Antarctissa deflandrei (Petrushevskaya) n. comb.<br />
Ling, H.Y. & Lazarus, D.B. 1990. Cretaceous<br />
<strong>radiolaria</strong> from the Weddell Sea: Leg 113 of the Ocean<br />
Drilling Program. In: Proceedings of the Ocean Drilling<br />
Program, Scientific Results. (Barker, P.F., Kennett, J.P. et<br />
al., Eds.), vol. 113. College Station, TX (Ocean Drilling<br />
Program), pp. 353-363.<br />
Unusually well preserved Cretaceous <strong>radiolaria</strong>ns are observed<br />
in the subsurface sections from two drilled sites in the Weddell Sea<br />
collected during Leg 113 of the Ocean Drilling Program. Radiolarians<br />
from the lithified calcareous chalk of Hole 689B represent the first<br />
Campanian-Maestrichtian assemblage which is characterized by<br />
abundant Cromyodruppa ? concentrica, Dictyomitra multicostata,<br />
and Protostichocapsa stocki. Abundant Pseudodictyomitra<br />
pentacolaensis and Diacanthocapsa sp. I, on the other hand, are the<br />
main constituents of the assemblage from the latest Aptian/earliest<br />
Albian diatomite of Hole 693B. These represent the oldest and the<br />
highest-latitude reported <strong>radiolaria</strong>n occurrences from the Atlantic<br />
sector of the Antarctic Ocean. The assemblages are marked by their<br />
low diversity and an absence of low- to mid-latitude zonal indices.<br />
- 51 -<br />
Marcucci, M. & Marri, C. 1990. Radiolarian<br />
assemblages in ophiolite sequences of southern Tuscany: new<br />
data. Ofioliti, 15/1, 185-190.<br />
The ophiolites of the Northern Apennines are topped by a<br />
siliceous sedimentary formation: the M. Alpe Cherts (Abbate and<br />
Sagri, 1970). This paper concerns the age of the base of this<br />
formation in Southern Tuscany, that is the onset of siliceous<br />
deposition above the ophiolite sequence in this area. Datings are<br />
based on <strong>radiolaria</strong>n biostratigraphy of Baumgartner (1984; 1987).<br />
Three new sections of the M. Alpe Cherts are examined: Il Romito,<br />
near Leghorn (Fig. 2a), Capannelle, near Paganico (Fig. 2b), Sovana-<br />
Elmo, SE of M. Amiata (Fig. 2c). Other sections in Southern Tuscany<br />
have been previously studied: Elba Island (Baumgartner, 1984; Conti<br />
and Marcucci, 1986), M. Vitalba (Picchi, 198S), Riparbella and<br />
Quercianella (Nozzoli, 1986), Murlo (Conti and Marcucci, 1986),<br />
(Fig. 1).<br />
Margulis, L., Corliss, J.O., Melkonian, M. &<br />
Chapman, D.J. 1990. Handbook of Protoctista: the<br />
structure, cultivation, habitats, and life histories of the<br />
eukaryotic microorganisms and their descendants exclusive of<br />
animals, plants and fungi: a guide to the algae, ciliates,<br />
foraminifera, sporozoa, water molds, slime molds, and the<br />
other protoctists. The Jones and Barlett Series in Life<br />
Sciences, Jones and Barlett Publishers Boston. , 914 p.<br />
Matsuoka, A. 1990. Explanatory Notes, Shipboard<br />
Scientific Party. In: Proceedings of the Ocean Drilling<br />
Program, Initial Reports. (Larson, R.L., Lancelot, Y. et al.,<br />
Eds.), vol. 129. College Station, TX (Ocean Drilling<br />
Program), pp. 5-29.<br />
In this chapter, we have assembled information that will help<br />
the reader understand the basis for our preliminary conclusions and<br />
also help the interested investigator select samples for further<br />
analysis. This information concerns only shipboard operations and<br />
analyses described in the site chapters in the Initial Reports volume<br />
of the Leg 129 Proceedings of the Ocean Drilling Program. Methods<br />
used by various investigators for shore-based analysis of Leg 129<br />
data will be detailed in the individual scientific contributions<br />
published in the Scientific Results volume.<br />
Cenozoic Zonation: Radiolarian zonal assignments of Cenozoic<br />
samples were based on the tropical zonation of Riedel and Sanfilippo<br />
(1978) and subsequent modification in Sanfilippo et al. (1985).<br />
Calibration of this zonation with chronostratigraphy and<br />
geochronology follows Berggren et al. (1985a, 1985b).<br />
Mesozoic Zonation: Figures 9 and 10 show the <strong>radiolaria</strong>n<br />
zonation scheme adopted during Leg 129 for Middle Jurassic to<br />
Cretaceous sediments and the calibration with the geochronology of<br />
Kent and Gradstein (1985). The zonation of Sanfilippo and Riedel<br />
(198S) was applied to the Cretaceous sediments except for the<br />
Berriasian and early Valanginian. For the Middle Jurassic to early<br />
Valanginian interval, the <strong>radiolaria</strong>n zonation of Matsuoka and Yao<br />
(1985, 1986) was adopted with modifications. The lowermost<br />
Cretaceous Pseudodictyomitra carpatica Zone is here defined as an<br />
interval zone, although it was originally defined as an assemblage<br />
zone (Matsuoka and Yao, 1985). Its base and top are limited by the<br />
first occurrences of P. carpatica and Cecrops septemporatus,<br />
respectively. The top of the uppermost Jurassic Pseudodictyomitra<br />
primitiva Zone is defined by the first occurrence of P. carpatica .<br />
Age determinations of sediments for the Middle Jurassic to<br />
early Valanginian interval are tentative because <strong>radiolaria</strong>n zones of<br />
this interval are not sufficiently dated by other age diagnostic<br />
fossils. Age assignments of sediments depended largely on<br />
correlation of Matsuoka and Yao's zonation with Baumgartner's<br />
(1984, 1987) zonation. His zonation was based primarily on his<br />
research of Atlantic and Mediterranean Tethys regions where<br />
<strong>radiolaria</strong>n-bearing sequences contain other age diagnostic fossils.<br />
Matsuoka, A. & Oji, T. 1990. Middle Jurassic <strong>radiolaria</strong><br />
fossils from the Magisawa Formation in the Taro Belt, North<br />
Kitakami Mountains. J. geol. Soc. Japan, 96/3, 239-241. (in<br />
Japanese)<br />
Matsuoka, A. & Yao, A. 1990. Southern Chichibu<br />
Terrane. In: Pre-Cretaceous Terranes of Japan. Publication of<br />
IGCP Project No. 224: Pre-Jurassic Evolution of Eastern Asia.<br />
(Ichikawa, K., Mizutani, S., Hara, I., Hada, S. & Yao, A.,<br />
Eds.). IGCP Project 224, Osaka, Japan. pp. 203-216.<br />
The Southern Chichibu Terrane (Fig. l) occupies southern<br />
marginal portion of the Jurassic-early Cretaceous terranes of<br />
Southwest Japan. Until 1970s, rocks in the terrane were believed to<br />
contain a small amount of age-diagnostic fossils except for late
Bibliography - 1990 Radiolaria 14<br />
Paleozoic fusulinids-corals and Triassic corals and other fossils<br />
from limestone blocks and the Late Jurassic marine fauna of the<br />
Torinosu Group. However, since the end of 1970s, as soon as it was<br />
recognized that this terrane is abundant in rocks yielding wellpreserved<br />
microfossils, especially <strong>radiolaria</strong>ns, great efforts have<br />
been made to carry out the reexamination of stratigraphy, geologic<br />
structure and geologic age mainly by means of <strong>radiolaria</strong>n<br />
biostratigraphy. As a result, our knowledge of this terrane has been<br />
rapidly advanced<br />
Matul', A.G. 1990a. Radiolaria thanatocenosises of<br />
sediment surface layer in the North Atlantic as reflection of<br />
environmental conditions. Okeanologiya, 30/1, 102-107.<br />
(in Russian)<br />
Four climatic groups of <strong>radiolaria</strong>ns, characterised by their<br />
attribution to some intervals of yearly average surface water<br />
temperature (subarctical, boreal, subtropical and tropical), are<br />
distinguished using data on quantitative distribution in surface<br />
sediment layer of 31 abundant species. Accordingly to changes of<br />
interrelations of these climatic groups in the modern<br />
thanatocoenoses the types of <strong>radiolaria</strong>ns thanatocoenoses are<br />
revealed, regions of which spreading are correspondent to climatic<br />
zones of the North Atlantic.<br />
Matul', A.G. 1990b. Radiolaria thanatocenoses in the<br />
surface layer of the North Atlantic sediments as a reflection of<br />
natural environmental conditions. Oceanology, 30/1, 76-79.<br />
On the basis of data on the quantitative distribution of 31 very<br />
common species in the surface layer of the sediments, four climatic<br />
groups of <strong>radiolaria</strong>ns are distinguished, each of them characterized<br />
by confinement to particular intervals of the mean annual<br />
temperature of the surface water: subarctic, boreal, subtropical and<br />
tropical. From the changes in ratios of these groups in the Recent<br />
thanatocenoses, types of Radiolaria thanatocenoses were found,<br />
whose geographic ranges in the sediments on the whole correspond<br />
to the climatic zones of the North Atlantic. By the graphs of the<br />
distribution of climatic groups in the Recent sediments, it appears to<br />
be possible to reconstruct the paleotemperatures by studying the<br />
paleothanatocenoses. The accuracy of the method is: ≤ ± 1,0° in 64-<br />
76%, ≤ ±1,5° in 75-80%, and ≤ ±2,0° in 84-92% of the<br />
calculations.<br />
Michalik, J., Gasparikova, V., Halasova, E.,<br />
Petercáková, M. & Ozvoldová, L. 1990.<br />
Microbiostratigraphy of the Upper Jurassic and Lower<br />
Cretaceous formations in the Manín unit, Mt. Butkov section<br />
(Strazovské Vrchy Mts., central West Carpathians). Knih.<br />
zemního plynu a nafty, 96, 23-55. (in Czech)<br />
This paper is a continuation of systematic stratigraphical<br />
research of Upper Jurassic—Lower Cretaceous sequence In the<br />
Butkov section. Several results Or study o~ ammonites, belemnites,<br />
crinoids, tintinnids and other calcareous microplankton have been<br />
published in the last years (Vasicek et al., 1983; Vasicek &<br />
Michalik, 1988; Borza et al., 1987; Zitt & Michalik,1988, Michalik &<br />
Vasicek, 1989 etc). This contribution is focused on the<br />
microplankton and nannoplankton remnants.<br />
The <strong>radiolaria</strong>ns occur in all the formations studied. However,<br />
only uncalcified <strong>radiolaria</strong>ns have been able to be separated and<br />
identified. The <strong>radiolaria</strong>n associations from Czajakowa, Ladce,<br />
Mraznica, Kalisco, and Luckovska Formations were the best<br />
preserved. Those of the Czajakowa Formation represent Late<br />
Oxfordian U.A.7 and U.A.8. Ladce and Mraznica Formations contain<br />
dispersed, often poorly preserved <strong>radiolaria</strong>ns of general Lower<br />
Cretaceous type. 26 <strong>radiolaria</strong>n species belonging to Late Early<br />
Hauterivian Mirifusus chenodes Zone come from the Kalisco<br />
Formation. The richest associations (38 <strong>radiolaria</strong>n taxa) have been<br />
obtained from the Luckovskci Formation. Except of Barremian types,<br />
several Hauterivian species Acanthocircus dicranacanthos, Ac.<br />
carinatus, Obesacapsula rotunda, and Cecrops septemporatus are<br />
present in those associations. They are supposed to be derived from<br />
older limestone clasts.<br />
No nannoplankton have been found in Upper Jurassic beds.<br />
Ladce Formation yielded a poor association dominated by<br />
Waznaueria barnesae, Micrantholithus hochschulzi and Nannoconus<br />
steinmanni. Almost Identical associations occur In both the Mraznica<br />
and Kalisco Formations: sole occurrences of Calcicalathina<br />
oblongata, Conusphaera mexicana, Cruciellipsis cuvillieri enrich<br />
them in the last one. This association could indicate Hauterivian-<br />
Barremian boundary in the upper part of the Kalisco formation. A<br />
similar, even more diversified association comes from the<br />
Luckovska Formation. It Is enriched by Braarudosphaera bigelowi and<br />
by sole Calcicalathina oblongata. Calcitic nannoplankton of all the<br />
formations is represented by robust, thick forms, which were<br />
resistant to dissolution and diagenesis. Cruciellipsis cuvillieri and<br />
- 52 -<br />
Conusphaera mexicana have been here described for the first time<br />
from the west Carpathian territory. The former one is a valuable<br />
Early Berriasian—Late Hauterivian Index species. The facts obtained<br />
make the biostratigraphical knowledge of the Upper Jurassic—Lower<br />
Cretaceous sequence in the Manin Unit (and in the West Carpathians<br />
as a whole) more complete. However, refining of Lower Cretaceous<br />
nannoplankton biostratigraphical scale needs further, more detailed<br />
study with the use of S.E.M.<br />
Mizutani, S. 1990. Mino Terrane. In: Pre-Cretaceous<br />
Terranes of Japan. Publication of IGCP Project No. 224: Pre-<br />
Jurassic Evolution of Eastern Asia. (Ichikawa, K., Mizutani,<br />
S., Hara, I., Hada, S. & Yao, A., Eds.). IGCP Project 224,<br />
Osaka, Japan. pp. 121-135.<br />
Murchey, B.L. 1990. Age and depositional setting of<br />
siliceous sediments in the upper Paleozoic Havallah sequence<br />
near Battle Mountain, Nevada; implications for the<br />
paleogeography and structural evolution ofthe western<br />
margin of North America. Geol. Soc. Amer., spec. Pap., 255,<br />
137-155.<br />
The upper Paleozoic Havallah sequence of central Nevada is a<br />
folded and thrust-faulted association of greenstone, siliceous<br />
marine sedimentary rocks, and deepwater clastic rocks. Microfossil<br />
assemblages (<strong>radiolaria</strong>ns, sponge spicules, and conodonts as tools<br />
to unravel the stratigraphy and to interpret the paleoenvironments<br />
of the siliceous sedimentary rocks. Nine <strong>radiolaria</strong>n assemblages<br />
(Osagean to Guadalupian) are described and used for delineation and<br />
correlation of fault-bounded lithotectonic units. The biostratigraphic<br />
zonation reveals that the oldest rocks in each lithotectonic unit are<br />
progressively younger from the structurally highest to the lowest<br />
units, suggesting progressive west-to-east upsection stepping of<br />
the Golconda sole thrust with accretion of each unit. Analyses of the<br />
<strong>radiolaria</strong>n and sponge spicule faunas permit lateral and temporal<br />
comparisons of depositional environments. The lower structural<br />
units are coarsening-upward sequences of hemipelagic slope<br />
deposits overlain by sponge spicule-rich turbidites derived from a<br />
shallow source. The uppermost structural unit is a coarseningupward<br />
basinal sequence. Permian sponge spicules in turbidites of<br />
the slope sequences and redeposited fusulinids in the basin<br />
sequence are similar to those in adjacent autochthonous (North<br />
American) regions. Permian <strong>radiolaria</strong>ns and sponge spicules in<br />
hemipelagic siliceous argillite of the slope sequences are similar to<br />
those in the Northern Sierra terrane to the west; the Havallah basin<br />
and the Northern Sierra arc terrane were overlain, therefore, by a<br />
similar water mass and may have been in proximity during the<br />
Permian. Clastic dikes and sills containing volcanic, metamorphic,<br />
and sedimentary rock clasts are Leonardian or younger.<br />
Nagai, H. 1990. Jurassic (Lower Toarcian) Radiolarians<br />
from the Hyde Formation, central Oregon, North America.<br />
Bull. Nagoya Univ. Furukawa Mus., 6, 1-19. (in Japanese)<br />
Radiolarian fossils in the Jurassic (lower Toarcian) Hyde<br />
Formation of Oregon were examined. It is detected that the<br />
<strong>radiolaria</strong>ns belonging to Eucyrtidiellum sp. C group of Nagai (1986)<br />
are contained in sample OR-600 in the lower part of the Hyde<br />
Formation. E. sp. C 2 seems to be a marker species which indicates a<br />
stratigraphic horizon ranging in age from upper Pliensbachian to<br />
lower Toarcian.<br />
Nagai, H. & Mizutani, S. 1990. Jurassic Eucyrtidiellum<br />
(Radiolaria) in the Mino Terrane. Trans. Proc. palaeont. Soc.<br />
Japan, n. Ser., 159, 587-602.<br />
Jurassic Eucyrtidiellum in chert, siliceous shale and manganese<br />
carbonate rock in the Mino terrane of central Japan was studied<br />
together with that of the Snowshoe Formation of Oregon with the<br />
result that eighteen species are recognized in the early Late to<br />
Upper Jurassic formations. Of all these species, Eucyrtidiellum<br />
disparile, E. unumaense, E. pustulatum, E. semifactum and E. ptyctum<br />
are most prevalent. These species are morphologically related with<br />
each other, and show an evolutionary trend composed of two<br />
consecutive steps of change, early in shell structure of abdomen,<br />
represented by transition from E. disparile to E. unumaense and later<br />
in superficial plication of abdomen, represented by transition from E.<br />
pustulatum through E. semifactum to E. ptyctum. On the basis of<br />
occurrence of E. pustulatum in the upper Bathonian part of the<br />
Snowshoe Formation, <strong>radiolaria</strong>n biostratigraphical correlation for<br />
the Japanese Jurassic formations is discussed. Two new species,<br />
Eucyrtidiellum disparile and E. semifactum, are described in this<br />
paper together with other species relevant to them.<br />
Nakae, S. 1990. Melanges in the Mesozoic sedimentary<br />
complex of the northern part of the Tamba Belt, southwestern<br />
Japan. J. geol. Soc. Japan, 96/5, 353-369. (in Japanese)
Radiolaria 14 Bibliography - 1990<br />
The Triassic to Jurassic sedimentary complex in the northern<br />
part of the Tamba Belt, Southwest Japan, is divided into the<br />
Yuragawa, Tsurugaoka, Hisasaka Complexes and the Furuya<br />
Formation. These complexes are composed mainly of melange,<br />
forming a pile of nappes. These melanges, chaotically mixed rock<br />
bodies, have been composed of the constituent element of the<br />
Triassic to Jurassic chert-clastics sequences ranging from pelagic<br />
siliceous rock upward to terrigenous clastic rock. On the basis of<br />
<strong>radiolaria</strong>n biostratigraphy, the age of clastic rocks of these<br />
complexes indicates younging overall toward the structural lower,<br />
namely from the Hisasaka Complex to the Yuragawa Complex. Many<br />
deformation structures are recognized in the melange; layer-parallel<br />
extension and shearing produced disruption of the original layering in<br />
the clastic rocks. Asymmetric deformation structures originating<br />
during the layer-parallel shearing are inferred to have been formed<br />
as a result of the compression probably associated with a northward<br />
underthrusting or southward overthrusting. These lithologic and<br />
structural features suggest that the sedimentary complex in this<br />
area is interpreted to have primarily been formed at an ancient<br />
subduction zone.<br />
Nelson, D.M. & Gordon, L.I. 1990. Distributions of<br />
biogenic silica and dissolved silicic acid in the surface waters<br />
of the Ross Sea, January and February 1990. Antarct. J. U. S.,<br />
25/5, 98-99.<br />
Global mass balances indicate that approximately 75-85<br />
percent of the modern accumulation of biogenic silica in marine<br />
sediments takes place south of the Antarctic Convergence (De<br />
Master 1981; Ledford-Hoffman, De Master, and Nittrouer 1986).<br />
The antarctic and subantarctic are nowhere near this important<br />
quantitatively in the global deposition pattern of organic carbon<br />
(Lisitzin 1972; Holland 1978), and appear to account for no more<br />
than 5 percent of the global-scale photosynthetic production of<br />
organic carbon by phytoplankton (Smith and Nelson 1986). These<br />
mass-balance calculations combine to suggest that the cycles of<br />
siliceous and organic biogenic material in the southern ocean are<br />
decoupled to an extent that is not true in most other oceanic<br />
regions, and that this decoupling makes the Antarctic the main site<br />
of long-term removal of silica from the oceans.<br />
Nishimura, H. 1990. Taxonomic study on Cenozoic<br />
Nassellaria (Radiolaria). Sci. Rep. Inst. Geosci., Univ.<br />
Tsukuba, Sect. B: geol. Sci., 11, 69-172.<br />
Well-preserved and highly diversified Cenozoic nassellarians<br />
extracted from the following formations and deep-sea sediments are<br />
comprehensively studied: Hatatate Formation of Miyagi Prefecture,<br />
Isozaki Formation of Ibaraki Prefecture; Zushi and Kinugasa<br />
Formations of Kanagawa Prefecture; deep-sea bottom sediments at<br />
Lat. 0° 58' S, Long. 18° W, depth 5359 m and at Lat. 0° 55.96' S,<br />
Long. 166°15.77' W, depth 5,405 m. The present author observed<br />
the ultramicrostructures of cephalic wall and skeleton of these<br />
<strong>radiolaria</strong>ns with a scanning electron microscope. As a result, the<br />
following three lines of evidence are clarified; (1) three patterns of<br />
growth lines are recognized; (2) traces of the vertical, apical, dorsal,<br />
lateral and secondary lateral rays are detected; (3) elongated rays<br />
of the cephalic skeleton are recognized within the cephalic wall. This<br />
evidence shows that the cephalic skeletal structures are formed in<br />
the earliest growth stage of shell and gradually covered by lamellae.<br />
Therefore, the cephalic skeletal structures are considered to be the<br />
most important criterion for higher taxonomy of nassellarians.<br />
Fifteen types of the cephalic skeletal structures are distinguished in<br />
Cenozoic nassellarians, which are classified into 15 families.<br />
In the present study, 58 genera and 112 species of<br />
nassellarians are studied, of these 6 genera and 4 species are newly<br />
proposed and 52 genera are emended herein. Based upon the<br />
cephalic skeletal structures, 13 families are emended and 2 new<br />
families are proposed herein.<br />
Noble, P. & Renne, P. 1990. Paleoenvironmental and<br />
biostratigraphic significance of siliceous microfossils of the<br />
Permo-Triassic Redding Section, Eastern Klamath Mountains,<br />
California. Mar. Micropaleontol., 15/3-4, 379-391.<br />
Permo-Triassic rocks of the Redding Section, Eastern Klamath<br />
Mountains represent a vertical succession from a shallow water<br />
carbonate environment of the McCloud Limestone to a deeper water<br />
environment of the Pit Formation. This resulted from an episode of<br />
subsidence which started in the Early Permian and continued through<br />
the Middle Triassic. Subsidence is demonstrated by the existence of<br />
a set of progressively deepening lithofacies in Dekkas and basal Pit<br />
cherts. Dekkas cherts are hematitic with abundant sponge spicules<br />
and <strong>radiolaria</strong>ns indicative of highly oxygenated waters in full<br />
communication with oceanic circulation. Basal Pit cherts are pyritic,<br />
spicule-poor and fine grained, indicative of poorer circulation and<br />
greater depths. Extensive pyritic black shales of the Pit and Modin<br />
Formations overlie the basal Pit cherts and correspond to a<br />
- 53 -<br />
restriction of circulation resulting in the stagnation of bottom water<br />
and the development of anoxic conditions. Normal marine circulation<br />
returned briefly in the Late Triassic as evidenced by the Hosselkus<br />
Limestone, a fossiliferous micritic limestone containing abundant<br />
marine fauna, including <strong>radiolaria</strong>ns.<br />
Radiolarians recovered from Dekkas cherts are sufficiently well<br />
preserved to yield an age of early Guadalupian, based on Albaillellid<br />
fauna. This fauna was calibrated with a fusulinid fauna collected 7<br />
km south in the lower section of the same member. One new genus<br />
and three new species are described.<br />
O'Dogherty, L. & Martínez-Gallego, J. 1990.<br />
Radiolarios del Cretácico Inferior (Barremense-Albense) en el<br />
sector de Campillo de Arenas (Subbético Medio). Acta<br />
Salmanticensia, 68, 263-275.<br />
The Barremian-Lower Albian Radiolaria fauna from the Campillo<br />
de Arenas area (Middle Subbetic) is studied for the first time. Three<br />
faunal assemblages have been recognized. A lower one (Barremianlower<br />
Aptian) which is dominated by, Sphaerostylus septemporatus,<br />
S. Ianceola, Eucyrtis hanni and Archaeodictyomitra lacrimula. A<br />
middle (upper Aptian) where Thanarla conica and Thanarla pulchra<br />
are the more characteristic species; and a upper one (lower Albian)<br />
with Kozurium ssp. These Radiolarian faunas bear great affinities to<br />
the North California and Central America ones.<br />
Okada, M. 1990. Occurrence of Permian <strong>radiolaria</strong>ns from<br />
Ujitawara-cho, southern Kyoto Prefecture. J. geol. Soc.<br />
Japan, 96/11, 937-939. (In Japanese)<br />
Osozawa, S., Sakai, T. & Naito, T. 1990. Miocene<br />
subduction of an active mid-ocean ridge and origin of the<br />
Setogawa ophiolite, Central Japan. J. Geol., 98/5, 763-771.<br />
The Setogawa subduction complex represents the subduction of<br />
an active mid-ocean ridge (the Kula Pacific Ridge) under the Japan<br />
Arc about 20 m.y. ago in the early Miocene. The basalt is youngest in<br />
subzone B3 of the Setogawa Belt and becomes older in both landward<br />
and oceanward subzones. Accumulation time for pelagic sediments<br />
overlying the basalt lengthens in the same two directions. The basalt<br />
of subzones B2 and B3 is directly overlain by or contemporaneous<br />
with the hemipelagic sediments. In subzone B3. the Setogawa<br />
dismembered ophiolite, including basalt, ultramafic rocks, gabbro,<br />
tonalite, and trondhjemite was emplaced from the mid-ocean ridge<br />
near the subduction zone.<br />
Ozvoldová, L. 1990. Radiolarian microfauna from<br />
radiolarites of the Varin part of the west Carpathian Klippen<br />
Belt. Geol. Sb. (Bratislava), 41/3, 295-310.<br />
In the drillhole Smolinske 17 at a depth of 1399—1605 m,<br />
marlstones, marly shales and limestones of Albian age with<br />
<strong>radiolaria</strong>n ostracod and foraminifer microfauna have been found<br />
under Neogene sediments of the Vienna Basin (BieIy et al., 1973).<br />
The composition of the foraminifer microfauna determined by SamueI<br />
(ibidem) suggests its Albian age. The analysis of the well-preserved<br />
pyritized <strong>radiolaria</strong>n microfauna from a depth of 1498-1499 m<br />
indicates also the Albian, probably its middle to upper part.<br />
Ozvoldová, L. 1990. Occurrence of Albian <strong>radiolaria</strong> in<br />
the underlier of the Vienna Basin. Geol. Sb. (Bratislava),<br />
41/2, 137-154.<br />
Microfaunistic analysis of samples from radiolarites and<br />
<strong>radiolaria</strong>n limestones of the Kysuca succession in the western part<br />
of the Varin stretch of the Klippen Belt at localities Brodno, Sneznica<br />
and Lopusne Pazite has proved the presence of <strong>radiolaria</strong>n<br />
microfauna which can be correlated, according to biostratigraphic<br />
zoning of Baumgartner (1984), with U.A. 7 and U.A. 8<br />
stratigraphically corresponding (Baumgartner, 1987) to the upper<br />
part of the Lower to Upper Oxfordian. A new species ?<br />
Angulobracchia cava n. sp. has been described in the assemblage of<br />
the sample S-4 (Sneznica).<br />
Pessagno, E.A. & Blome, C.D. 1990. Implications of<br />
New Jurassic stratigraphic, geochronometric, and<br />
paleolatitudinal data from the western Klamath terrane (Smith<br />
River and Rogue Valley subterranes). Geology, 18, 665-668.<br />
Combined biostratigraphic, chronostratigraphic, and<br />
geochronometric studies of the Rogue and Galice Formations (Rogue<br />
Valley subterrane, southwestern Oregon) indicate that the<br />
Oxfordian-Kimmeridgian boundary should be placed at 154 +1.5 Ma<br />
rather than at 156 +6 Ma as advocated in the Decade of North<br />
American Geology 1983 geologic time scale. In the Smith River<br />
subterrane (northwestern California, southwestern Oregon), well-
Bibliography - 1990 Radiolaria 14<br />
preserved Radiolaria were recovered not only from strata overlying<br />
the Josephine ophiolite, but also from within the volcanic member of<br />
the ophiolite. U/Pb geochronometric data constrain the age of the<br />
Mirifusus first-occurrence event to after 162 ± 1 Ma and to being<br />
157 ±1.5 Ma or slightly older. Radiolarian faunal data indicate that<br />
the Josephine ophiolite originated at Central Tethyan paleolatitudes<br />
during the latest Callovian (162 Ma) and was carried northward to<br />
Northern Tethyan and Southern Boreal paleolatitudes during the<br />
Oxfordian.<br />
Petercáková, M. 1990. Radiolarian from cherts of the<br />
Kalisco limestone formation of the Manin unit (Butkov,<br />
West Carpathians). Geol. Sb. (Bratislava), 41/2, 155-169.<br />
The work deals with the first occurrence of <strong>radiolaria</strong>ns in the<br />
Lower Cretaceous pelagic sediments of the Manin unit of the West<br />
Carpathians. The <strong>radiolaria</strong>ns come from cherts of Kalisco<br />
Limestones that in the past were stratigraphically investigated by<br />
means of ammonites and tintinnoid organisms (Vasicek—Michalik,<br />
1986; Borza et al., 1987). Radiolarian species characterizing the<br />
zone Mirifusus chenodes (sensu SCHAAF, 1984) were identified,<br />
which stratigraphically corresponds to the uppermost part of the<br />
Lower Hauterivian.<br />
Petrushevskaya, M.G. & Swanberg, N.R. 1990.<br />
Variability in skeletal morphology of colonial Radiolaria<br />
(Actinopoda: Polycystinea: Collosphaeridae).<br />
MIcropaleontoloy, 36/1, 65-85.<br />
Skeletal morphology is used to determine species in almost all<br />
Radiolaria, and in many cases relatively fine differences between<br />
morphotypes are used to distinguish between species. While many<br />
Radiolaria have been described from very few specimens we have<br />
little knowledge of variability of Radiolaria because we have been<br />
able to study few known biological populations of a species. This<br />
problem has been addressed by examining the variation occurring<br />
within colonies of collosphaerid Radiolaria, and comparing it to that<br />
occurring between colonies of the same and other species. As far as<br />
we know the cells within such colonies are genetically identical and<br />
therefore intra-colony variation must be caused by other than<br />
species-level phenomena.<br />
Both quantitative and qualitative features were considered in a<br />
detailed study of a total of 2922 skeletons in 44 colonies<br />
representing 12 species. The results of this analysis have revealed<br />
substantial variation in both quantitative and qualitative features,<br />
both between and within colonies of a species. Furthermore, typically<br />
1-5% and sometimes even 10-20% of the individuals in a colony<br />
possess some structures which are absent in the majority of<br />
individuals of the species. The structures which are characteristic<br />
for one species, typically occurred at a low rate in another. No<br />
smooth transition between species was seen provided that one<br />
considered the whole suite of diagnostic morphological features and<br />
not just a single character. Caution is strongly urged in uncertain<br />
species assignments and it is asserted that it is absolutely<br />
impossible to erect new species on the basis of a few specimens<br />
which are non-identical, or on the appearance of a single feature.<br />
Raymond, D. & Lethiers, F. 1990. Signification<br />
géodynamique de l'événement radiolaritique dinantien dans les<br />
zones externes sud-varisques (Sud de la France et Nord de<br />
l'Espagne). C.R. Acad. Sci. (Paris), Sér. II, 310, 1263-1269.<br />
In the South of France and the North of Spain the radiolarites<br />
from Dinantian age have been deposited in a narrow basin initiated<br />
since the Frasnian times and bordered by emerged areas. The<br />
starting of the siliceous deposition would be related to the<br />
installation of cold deep-water currents coming from a Late<br />
Devonian-Early Carboniferous glacial North-Gondwanian area.<br />
Special ostracod faunas corroborate these paleoecologic changes.<br />
Renz, G.W. 1990. Ordovician Radiolaria from Nevada and<br />
Newfoundland a comparison at the family level. Mar.<br />
Micropaleontol., 15/3-4, 393-402.<br />
Two Ordovician <strong>radiolaria</strong>n assemblages from North America<br />
are examined and compared at the family (group) level. In the<br />
material from Newfoundland (Middle Ordovician—Llanvirnian, after<br />
Bergstrom, 1974), well-preserved specimens are common, 92%<br />
being spherical polycystines. In the Nevada material (Upper<br />
Ordovician—Caradocian, after Dunham and Murphy, 1976), wellpreserved<br />
specimens are abundant and coated with iron oxide. Here<br />
species of spherical polycystines constitute only 42% of the<br />
population while species of Palaeoscenidiidae, after their appearance<br />
and radiation within the preceding 25 million years, constitute 47%.<br />
Results of this comparison at the family level suggest that for<br />
<strong>radiolaria</strong>ns, evolutionary change during the Ordovician was not slow<br />
- 54 -<br />
as previously thought. Rather, this was a time of growth, radiation<br />
and experimentation.<br />
Riedel, W.R. 1990. Quantitative description of pore<br />
patterns in <strong>radiolaria</strong>. Micropaleontology, 36/2, 177-181.<br />
The arrangement of pores in the lattice-shells of <strong>radiolaria</strong>ns<br />
can be an important descriptor of the skeletons, if the pattern can<br />
be characterized quantitatively. An image analysis system<br />
integrated with a personal computer provides a convenient means of<br />
measuring distances between pores, and their angular relations,<br />
together with the variability of those measures. Both regular and<br />
irregular patterns can be quantified. The procedure is adaptable to a<br />
wide spectrum of patterns in the organic world.<br />
Sanfilippo, A. 1990. Origin of the subgenra<br />
Cyclampterium, Paralampterium and Sciadiopeplus from<br />
Lophocyrtis (Lophocyrtis) (Radiolaria, Theoperidae). Mar.<br />
Micropaleontol., 15/3-4, 287-312.<br />
Work on the exceptionally well-preserved, rapidly accumulating<br />
Bath Cliff Section, Barbados and supplementary Deep Sea Drilling<br />
Project samples, has revealed the evolutionary origins of three<br />
stratigraphically useful species in the Cryptoprora ornata Zone<br />
straddling the Eocene/Oligocene boundary and demonstrated the<br />
origin of the genus Cyclampterium. Elucidation of the origin of<br />
Cyclampterium milowi necessitates a revision of the genera<br />
Lophocyrtis and Cyclampterium. Lophocyrtis (Lophocyrtis) jacchia is<br />
the ancestor of L. (Cyclampterium) hadra, the earliest member in the<br />
subgenus Cyclampterium which comprises the anagenetic lineage<br />
leading from L. (C.) hadra to L. (C.) neatum. The monotypic subgenus<br />
Sciadiopeplus branches off from an early member in the<br />
Cyclampterium lineage. The new species L. (L.) exitelus and L. (S.)<br />
oberhaensliae terminate the subgenera Lophocyrtis and<br />
Sciadiopeplus, respectively. During the investigation it also became<br />
clear that morphotypes resembling early L. (C.) milowi could be<br />
found in mid and high latitude assemblages in the late Early and late<br />
Middle Eocene. The origin of one these morphotypes was also traced<br />
to L . (Lophocyrtis) jacchia giving rise to the new subgenus<br />
Paralampterium. This lineage includes the new species L .<br />
(Paralampterium) dumitricai and two species questionably assigned<br />
to it, L. (Paralampterium) ? Iongiventer and the new species L.<br />
(Paralampterium) ? galenum. The relationship of L. (P.) dumitricai to<br />
L. (P.) ? Iongiventer and L. (P.) ? galenum is unknown.<br />
Schwartzapfel, J.A. 1990. Biostratigraphic<br />
investigations of Late Paleozoic (Upper Devonian to<br />
Mississipian) Radiolaria within the Arbuckle Mountains and<br />
Ardmore. Ph.D Thesis. Programs in Geoscience, University<br />
of Texas at Dallas, p. (unpublished)<br />
Sedlock, R.L. & Isozaki, Y. 1990. Lithology and<br />
biostratigraphy of Franciscan-like chert and associated rocks<br />
in west-central Baja California, Mexico. Geol. Soc. Amer.,<br />
Bull., 102, 852-864.<br />
We present the result of biostratigraphic and lithologic studies<br />
of ribbon chert and associated rocks in a Mesozoic subduction<br />
complex in west-central Baja California, Mexico. The subduction<br />
complex terrane is divided into three subterranes, each of which<br />
consists of an originally coherent sequence of interbedded oceanic<br />
rocks, including ocean-floor basalt, terrigenous siliciclastic<br />
turbidites, <strong>radiolaria</strong>n ribbon chert, and limestone. Parts of the<br />
original stratigraphy are preserved in the least deformed, least<br />
metamorphosed subterrane. Ocean-floor pillow basalt on Cedros<br />
Island is overlain by about 40 m of <strong>radiolaria</strong>n ribbon chert ranging in<br />
age from Early Jurassic or older to Early Cretaceous; the chert is<br />
overlain by thin-bedded turbidites. On San Benito West Island,<br />
<strong>radiolaria</strong>n ribbon chert is interbedded with volcanogenic rocks,<br />
including a megabreccia that contains blocks of metabasites, folded<br />
Late Jurassic-Early Cretaceous chert, and marble in a mid-<br />
Cretaceous radiolarite matrix. Chert samples from tectonically<br />
thinned sequences elsewhere on Cedros and San Benito Islands<br />
contain Late Triassic to Early Cretaceous <strong>radiolaria</strong>n assemblages.<br />
The 40-m-thick chert section on Cedros Island probably<br />
accumulated atop oceanic crust in a large ocean basin for at least<br />
65 m.y. and was later capped by terrigenous turbidites as it<br />
approached the subduction zone along the western margin of North<br />
America. Faulted chert sections on Cedros and San Benito Central<br />
and West Islands are subsets of the main section on Cedros Island.<br />
The chert/megabreccia section on San Benito West Island is<br />
interpreted to have accumulated at the foot of a volcanic edifice on<br />
the ocean floor (for example, seamount, fracture zone) or during<br />
extension and normal faulting of the downgoing oceanic plate in a<br />
subduction zone. Sedimentary structures and stratigraphic relations<br />
indicate that all ribbon chert in this subduction complex was<br />
deposited by sediment gravity flows; that is, they are turbidites.
Radiolaria 14 Bibliography - 1990<br />
Sharma, V. & Mahapatra, A.K. 1990. Radiolarian<br />
occurrences in surface sediments of the Indian Ocean in<br />
relation to bottom water circulation. J. geol. Soc. India,<br />
35/3, 251-261.<br />
Occurrences of Radiolaria in the surface sediments collected at<br />
22 stations in the Indian Ocean are noted. While some samples<br />
contain abundant Radiolaria, others show extremely poor<br />
concentration, or, are practically devoid of them. A distinct<br />
relationship is found between <strong>radiolaria</strong>n abundance and deep water<br />
current systems. It is suggested that the occurrence of Radiolaria is<br />
largely controlled by currents which are responsible for dissolving<br />
<strong>radiolaria</strong>n skeletons. The assemblage is dominated by warm-water<br />
species and also contains a few cold water forms. The cold-water<br />
species are believed to be transported by the Antarctic Bottom<br />
Waters (AABW) to the present area.<br />
Skornyakova, N.S., Uspenskaya, T.Y.,<br />
Gorshkov, A.I. & Sivtsov, A.V. 1990. Ironmanganese<br />
concretions from the central trough of the Indian<br />
Ocean. Izv. Akad. Nauk SSSR, ser. geol., 6, 117-120. (in<br />
Russian)<br />
Examines the internal structure, chemical and mineral<br />
composition of concretions from the <strong>radiolaria</strong>n zone. Local<br />
variations in the concretions were noted. Sedimentational and<br />
diagenetic concretions were compared, and the conditions governing<br />
their formation were described.<br />
Smith, P.L. & Carter, E.S. 1990. Jurassic correlations<br />
in the Iskut River map area, British Columbia, and the age of<br />
the Eskay Creek deposit. Geol. Surv. Canada, curr. res., Pap.,<br />
90-1E, 149-151.<br />
A high-resolution, Jurassic biochronology based on macro- and<br />
microfossils could have important applications in the tectonically<br />
complex Iskut map area where Jurassic sediments accumulated in a<br />
shallow marine, volcanically active area characterized by rapid<br />
lateral variations in facies. Reconnaissance work in the upper<br />
drainage of the Unuk River has produced Pliensbachian to possibly<br />
Oxfordian age ammonite and <strong>radiolaria</strong>n faunas, some of which are<br />
anomalous with respect to currently available geological maps. The<br />
presence of Jurassic <strong>radiolaria</strong>ns in well-rounded clasts of Jurassic<br />
conglomerates may offer the opportunity of constraining periods of<br />
Jurassic tectonism. Upper Pliensbachian ammonites were collected<br />
stratigraphically below the Eskay Creek deposit. A limestone clast<br />
from a conglomerate above the deposit has yielded <strong>radiolaria</strong>ns that<br />
indicate a Middle Toarcian to Early Bajocian age.<br />
Spindler, M. & Beyer, K. 1990. Distribution,<br />
abundance and diversity of Antarctic acantharian cysts. Mar.<br />
Micropaleontol., 15/3-4, 209-218.<br />
Large numbers of acantharian cysts, up to more than 30<br />
individuals per m 3 , were collected during the austral summer<br />
(January-February) 1985 in the Weddell Sea, Antarctica by a<br />
multiple open-closing plankton net system. Stations were sampled<br />
17 days later in the season and revealed slightly higher abundances<br />
of cysts. Samples collected in the same region during winter and<br />
spring 1986 (July-November) contained no acantharian cysts. The<br />
numbers of cysts decreased from open ocean conditions to locations<br />
close to the ice shelf coast. Cysts were most abundant in water<br />
depths between 100 and 300 meters. The morphology of the cysts,<br />
constructed from differently shaped strontium sulfate plates or<br />
from amorphous strontium sulfate, is described and the taxonomy of<br />
the different types discussed.<br />
Stais, A., Ferriere, J., Caridroit, M., De Wever,<br />
P., Clement, B. & Bertrand, J. 1990. Données<br />
nouvelles sur l'histoire ante-obduction (Trias-Jurassique) du<br />
domaine d'Almopias (Macédoine, Grèce). C.R. Acad. Sci.<br />
(Paris), Sér. II, 310/11, 1457-1480.<br />
Chert beds from Almopias area have been dated with <strong>radiolaria</strong>n<br />
remains: some of them never described before. are Triassic (Vrissi<br />
Unit) while others, chert and volcanic beds from Mavrolakkos Unit<br />
are Jurassic early neocomian (probably Upper Jurassic). These<br />
results give some information on the unknown geological history of<br />
this area during Triassic-Jurassic times. They support the<br />
hypothesis of the existence of a Jurassic oceanic crust basin east of<br />
the Pelagonian zone, initiated during Triassic times. Finally, they<br />
modify the data used to discuss the existence of an Upper<br />
Cretaceous oceanic crust in the Alnlopias area.<br />
Swanberg, N.R., Anderson, O.R. & Bennett, P.<br />
1990. Skeletal and cytoplasmic variability of large<br />
- 55 -<br />
spongiose spumellarian <strong>radiolaria</strong> (Actinopodea:<br />
Polycystina). Micropaleontology, 36/4, 379-387.<br />
Large, spongiose skeletal Radiolaria occur abundantly in<br />
tropical and some subtropical oceanic locations. They are<br />
particularly conspicuous in plankton tows owing to their brightly<br />
coloured central capsular region (red to purplish-brown) and the<br />
numerous dinoflagellate, prymnesiophyte, or prasinophyte symbionts<br />
that impart a distinctly golden-brown or greenish hue to the<br />
peripheral cytoplasm. There is substantial variability in skeletal and<br />
cytoplasmic morphology and the major skeletal features used by<br />
Haeckel and others to discriminate among species intergrade to<br />
such a degree that it is not possible in most circumstances to make<br />
a clear taxonomic distinction. Furthermore, there is no correlation<br />
between the kind of symbiont associated with the host and its<br />
skeletal organization. Moreover, there is a nearly continuous<br />
variation in cytoplasmic organization of the central capsules varying<br />
from loosely organized radially arranged lobes surrounding a<br />
centrally located nucleus to a more spongiose and compact<br />
cytoplasm (consisting of interconnected masses of nucleated<br />
cytoplasm) with large, densely staining reserve bodies. In the<br />
extreme development of spongiose cytoplasmic organization, the<br />
reserve substance is dispersed throughout the cytoplasm. There is<br />
no correlation between the degree of spongiose quality of the<br />
cytoplasm and the organization of the skeleton. The variations in<br />
cytoplasmic organization suggest an ontogenetic sequence<br />
progressing from a large, centrally located nucleus with loose,<br />
radially-arranged cytoplasmic lobes toward increasingly dispersed<br />
nuclear lobes distributed into the peripheral cytoplasm containing<br />
abundant reserve bodies. Further research is needed to evaluate this<br />
hypothesis. In overall perspective, the variability among this group is<br />
so large and so intergraded that due caution is advised in assigning<br />
them to different species. Indeed, given the lack of clear skeletal<br />
and cytoplasmic demarcation within this group, and the absence of<br />
molecular genetic information to clarify the species affinities, it may<br />
be misleading to establish species based only on skeletal evidence.<br />
Moreover, further research is required to determine how much of the<br />
variation in skeletal structure can be attributed to genetic<br />
differences (taxonomic differences) versus ecophenotypic variation<br />
that may provide information about environmental variables<br />
recorded in the skeletal morphology.<br />
Tajika, J. & Iwata, K. 1990. Paleogene melange of the<br />
northern Hidaka Belt - Geology and <strong>radiolaria</strong>n age of the<br />
Kamiokoppe Formation. Mem. Hokkai Gakuen Univ., 66,<br />
35-55. (in Japanese)<br />
Geological and paleontogical investigation of the Hidaka<br />
Supergroup (Kamiokoppe Formation) in the Nishiokoppe area,<br />
northeast Hokkaido was carried out to examine sedimentary<br />
environment and to decide the age of the Hidaka Supergroup. The<br />
Kamiokoppe Formation consists of pillow basalt, red mudstone, and<br />
overlying repetitions of coarsening upward sequence of sandstone<br />
and mudstone. This formation includes a sedimentary melange called<br />
Honmanosawa melange, in which exotic olistoliths of limestone and<br />
chert are characteristically included. Paleocene <strong>radiolaria</strong>ns were<br />
extracted from the red mudstone of the Kamiokoppe Formation. This<br />
age may suggest the age of accumulation of the Kamiokoppe<br />
Formation. Triassic holothurian sclerites and <strong>radiolaria</strong>ns were<br />
discovered from blocks of limestone and chert in the Honmanosawa<br />
melange, and late Cretaceous <strong>radiolaria</strong>ns were also found from<br />
black mudstone of the same area, but matrix of this melange did not<br />
yet occur microfossils.<br />
Takahashi, K. 1990. Radiolarians from the distal Bengal<br />
Fan in the Equatorial Indian Ocean. In: Proceedings of the<br />
Ocean Drilling Program, Scientific Results. (Cochran, J.R.,<br />
Stow, D.A.V. et al., Eds.), vol. 116. College Station, TX<br />
(Ocean Drilling Program), pp. 207-209.<br />
Cores recovered from three sites of Leg 116 were studied for<br />
<strong>radiolaria</strong>ns. Generally, <strong>radiolaria</strong>ns were absent from most samples<br />
prepared for examination. Moderate to well-preserved <strong>radiolaria</strong>n<br />
assemblages are found only in the uppermost one or two cores that<br />
were the focus of this study. All of the <strong>radiolaria</strong>n assemblages in<br />
the upper cores belong to the Buccinosphaera invaginata Zone of<br />
latest Quaternary age. However, there is one stratum where a few<br />
Miocene <strong>radiolaria</strong>ns are reworked into the modern assemblages.<br />
Local seamounts are suggested sources for the reworked<br />
<strong>radiolaria</strong>ns.<br />
Takahashi, K., Billings, J.D. & Morgan, J.K.<br />
1990. Oceanic province: assessment from time-series diatom<br />
fluxes in the northeastern Pacific. Limnol. and Oceanogr.,<br />
35/1, 154-165.<br />
Samples were recovered from time-series sediment traps<br />
deployed simultaneously for one full year (l985-1986) at pelagic<br />
StationsPapa and C (~600 km apart) in the northeastern Pacific.
Bibliography - 1990 Radiolaria 14<br />
Species constituents, relative species contributions, and seasonal<br />
flux patterns of diatoms and other siliceous plankton are very much<br />
alike at the two sites. The level of similarity between the two sites is<br />
as close as that between two different depths at Station Papa,<br />
suggesting tightness of covariance between the two sites. It is<br />
possible to conclude that the oceanic flux province of the two sites<br />
is nearly the same and that the processes responsible for such<br />
similar export productions must be similar. Although quality of the<br />
fluxes is similar, the flux levels are not exactly the same at the two<br />
sites. Overall diatom export production at Station Papa was about<br />
twice that at Station C. Flux levels of Radiolaria and silicoflagellates<br />
were also higher at Station Papa than at Station C. Seasonal flux<br />
maxima at Station C were generally delayed by 2 1 weeks over those<br />
at Station Papa. The lower flux levels and delayed flux peaks at<br />
Station C are correlated with density structure of upper water<br />
masses.<br />
Takami, M., Isozaki, Y., Nishimura, Y. & Itaya,<br />
T. 1990. Geochronology of weakly metamorphosed Jurassic<br />
accretionary complex (the Kuga Group) in eastern Yamaguchi<br />
Prefecture, Southwest Japan. J. geol. Soc. Japan, 96, 669-<br />
681.<br />
Weakly metamorphosed Jurassic accretionary complex called<br />
the Kuga Group in eastern Yamaguchi Prefecture is composed mainly<br />
of olistostromal complex with matrices of mudstone and with<br />
allochthonous blocks of chert, sandstone, siliceous mudstone, black<br />
mudstone and greenstones. The northern part of this group<br />
(Northern Unit) is separated from the southern part (Southern Unit)<br />
by a north-dipping fault and is characterized by phyllitic nature of<br />
the rocks. Microfossil researches clarified that the<br />
Northern Unit contains Late Carboniferous to Late Triassic chert,<br />
Early Triassic and Late Triassic to Early Jurassic siliceous mudstone,<br />
and Early Jurassic black mudstone. Reconstructed primary<br />
stratigraphy of these rocks is identical to that of modern trench<br />
sediments. Although the age of matrices of mudstone has not been<br />
fixed, it is considered that the Northern Unit formed as an<br />
accretionary complex probably at early Middle Jurassic subduction<br />
zone. The rocks in the Northern Unit have undergone a high pressure<br />
type metamorphism of the pumpellyite-actinolite facies. K-Ar ages<br />
of recrystallized white micas from 18 phyllitic pelites in the<br />
Northern Unit concentrate in the range of 170-150 Ma (middle<br />
Middle to early Late Jurassic).<br />
Above-mentioned facts indicate that the Northern Unit of the<br />
Jurassic complex formed as an accretionary complex in early Middle<br />
Jurassic time and successively underwent a high pressure type<br />
metamorphism at the depth of subduction zone in middle Middle to<br />
early Late Jurassic time<br />
Takemura, A. 1990. Paleogene <strong>radiolaria</strong>n biostratigraphy<br />
in the Antartic Ocean regions. Kaiyo Monthly, 22, 263-270.<br />
(in Japanese)<br />
Tan, Z.Y. & Chen, M.H. 1990. Some revisions of<br />
Pylonidae. Chinese J. Oceanol. Limnol., 8/2, 109-127.<br />
The three faces of the Pylonid are similar to one another but<br />
actually have obvious differences. Their similarities and obvious<br />
differences in dorsal. Iateral, and apical views are the criteria for the<br />
author in species identification and redefinition of the Subfamilies<br />
Diplozonaria and Triplozonaria (6 species in all) and description of 7<br />
new species.<br />
Tipper, H.W. & Carter, E.S. 1990. Evidence for<br />
defining the Triassic-Jurassic boundary at Kennecott Point,<br />
Queen Charlotte Islands, British Columbia. Geol. Surv.<br />
Canada, curr. res., Pap., 90-1F, 37-41.<br />
At Kennecott Point in Queen Charlotte Islands, a minor<br />
discordance within sediments of the Sandilands Formation, Kunga<br />
Group is proposed as the Triassic-Jurassic boundary. Ammonites and<br />
<strong>radiolaria</strong>ns above the unconformity strongly indicate that the beds<br />
are earliest Hettangian in age; ammonites, conodonts, and<br />
<strong>radiolaria</strong>ns below the unconformity indicate that these beds are<br />
probably latest Triassic in age.<br />
Tominaga, R. 1990a. Jurassic accretionary prism of the<br />
northern part of the Chichibu Belt, eastern Shikoku. J. geol.<br />
Soc. Japan, 96/7, 505-522. (in Japanese)<br />
Geology of the Sawadani area, Eastern Shikoku, is described.<br />
And the province underlain by the Jurassic strata in the northern<br />
part of Chichibu Belt is redefined as an independent terrane based on<br />
the investigation in the Sawadani area. The Jurassic strata<br />
distributed in the Sawadani area are divided into three units, the<br />
Kenzan unit, the Higashiura unit and the Sawadani unit in ascending<br />
order. All boundaries of the units are thrust faults which dipped<br />
- 56 -<br />
south and were formed before the deposition of the Lower<br />
Cretaceous series over the Chichibu Belt.<br />
The Sawadani unit, which consists mainly of olistostromes with<br />
pelitic or psammitic matrices, is characterized by the occurrence of<br />
large amounts of greenstones, limestone and stratified serpentinite<br />
bodies associated with crystalline schists as olistoliths. The<br />
Higashiura unit is composed mainly of alternation of olistostromes<br />
with pelitic and psammitic matrices, and characteristically contains<br />
thick chert olistoliths associated with dolomite. The Kenzan unit also<br />
consists chiefly of olistostromes with pelitic matrices and abundant<br />
chert olistoliths, and contains intercalated acid tuff. Judging from<br />
<strong>radiolaria</strong>n fossils obtained from the Sawadani area, the Sawadani,<br />
Higashiura, and Kenzan units are dated as early to middle Early<br />
Jurassic, middle to late Early Jurassic, and Middle Jurassic age,<br />
respectively. In the Sawadani area, these units show the following<br />
four regularities regarding the ages of the constituent rocks: (1)<br />
Whithin each unit, sedimentation took place in the order of limestone<br />
⇒ chert ⇒ siliceous mudstone ⇒ mudstone. (2) Whithin each unit,<br />
there tends to be periods of overlapping sedimentation between<br />
limestone and chert, chert and siliceous mudstone, and siliceous<br />
mudstone and mudstone. (3) Of the same rock species, those in the<br />
lower unit are younger than those in the upper unit. (4) The rocks of<br />
the same kind in different units tend to have the overlapping periods<br />
of sedimentation. It is common among the accretionary prisms of<br />
other belts that constituent rocks have such regularities and that<br />
the unit boundaries are imbricated thrust faults. The model, which<br />
explains the regularity regarding the ages of the constituent rocks<br />
of the three units in the Sawadani area, illustrates the process of<br />
accumulation of the accretioary materials.<br />
Judging from the age polarity among the units, and from the<br />
content of the terigenous materials in each unit, the Sawadani unit,<br />
the Higashiura unit and the Kenzan unit are inferred to have<br />
accreted along the northern front of the land consisting mainly of<br />
the Kurosegawa rocks, during Early and Middle Jurassic time.<br />
Therefore, I propose to redefine the province, underlain by such<br />
Jurassic strata, as a terrane and to call the "Sawadani Terrane".<br />
Tominaga, R. 1990b. Tectonic development of the<br />
Chichibu belt, southwest Japan. J. Sci. Hiroshima Univ., Ser.<br />
C: Geol. Min., 9/2, 377-413.<br />
Tectonic development of the Chichibu belt, Southwest Japan<br />
was discussed in this paper. on the basis of analysis of<br />
tectonostratigraphic units and tectonic development of individual<br />
units of the Chichibu belt in Shikoku, clarifying following points.<br />
The Chichibu belt in Shikoku consists of three terranes, the<br />
Sawadani Terrane, the Kurosegawa Terrane and the Sambosan<br />
Terrane. The Sawadani Terrane is composed of three<br />
tectonostratigraphic units, which develop as nappes separated by<br />
southward dipping thrusts and show the northward younging age<br />
polarity. They in Eastern Shikoku correspond to the Sawadani unit of<br />
early to middle Early Jurassic time, Higashiura unit of middle to late<br />
Early Jurassic time and Kenzan unit of Middle Jurassic time in<br />
descending order, respectively. The Ohnogahara and Kanogawa<br />
nappes in Western Shikoku are correlated with the Sawadani and<br />
Higashiura nappes respectively. The ages of the constituent rocks of<br />
the nappes show following rules: (1) In each unit the age of the<br />
constituent rocks arrange in the order of limestone, chert, siliceous<br />
mudstone and mudstone from older to younger. (2) Each pair of<br />
limestone and chert, chert and siliceous mudstone and siliceous<br />
mudstone and mudstone of individual units tends to show the overlap<br />
of age. (3) The rocks of a kind in the lower unit are younger in age<br />
than those of the same kind in the upper unit. (4) The same sort of<br />
rocks in the different units tend to show the overlap of age. The<br />
Sawadani Terrane in Shikoku is defined as a belt occupied by Early to<br />
early Middle Jurassic accretionary prism formed along the northern<br />
(inner) front of the Kurosegawa Island-arc. The Kurosegawa Terrane<br />
is defined as a realm converted through Jurassic diastrophism from<br />
an older island-arc (Kurosegawa Island-arc), which consists of the<br />
Siluro-Devonian basement complex of continental crust type, Permo-<br />
Triassic continental shelf type sediments, Permo-Triassic<br />
accretionary prism etc. The Sambosan Terrane of the Hiradani-<br />
Shiraishi area, Eastern Shikoku, has been divided from north to south<br />
into the Torinosu Group and the A, B1, B2 and C tectonostratigraphic<br />
units. The A, B1, B2 and C units have lithological and chronological<br />
sequences regarded as accretionary prisms which show a younging<br />
age polarity from north to south. The Sambosan Terrane is defined as<br />
a belt which is occupied by Middle Jurassic to Early Cretaceous<br />
accretionary prism formed along the southern front of the<br />
Kurosegawa Terrane.<br />
Late Paleozoic to Mesozoic tectonic development of the<br />
Chichibu belt, Southwest Japan, is divided into nine stages. The initial<br />
structure of the Sawadani Terrane and the Sambosan Terrane were<br />
built up during the stages from 2 to 4 and the stages 5 to 7,<br />
respectively. And the diastrophism throughout the Chichibu belt had<br />
a climax at the change of the accretionary site from the northern<br />
(inner) side to the southern (outer) side across the Kurosegawa<br />
Terrane.
Radiolaria 14 Bibliography - 1990<br />
Tumanda, F.P., Sato, T. & Sashida, K. 1990.<br />
Preliminary late Permian <strong>radiolaria</strong>n biostratigraphy of the<br />
Busuanga Island, Palawan, Philippines. Annu. Rep. Inst.<br />
Geosci., Univ. Tsukuba, 16, 39-45.<br />
In the Philippines, Radiolaria have been used in establishing and<br />
checking its pre-Tertiary geology particularly in the North Palawan<br />
Block. Radiolaria were reported in the area and were used in the age<br />
determination of the rock units (Wolfart et al., 1986; Isozaki et al.,<br />
1988, Amiscaray and Tumanda, 1988; Cheng,1989). Although<br />
Cheng (1989) recognized 6 <strong>radiolaria</strong>n assemblages, no concrete<br />
biostratigraphic work has been published yet. In a preliminary work<br />
reported by the senior author during the 1989 Geological<br />
Convention in the Philippines, 8 <strong>radiolaria</strong>n assemblages were<br />
recognized. This paper presents the results of the paleontologic<br />
analyses of samples from the Permian sections in northern<br />
Mabintangin River, central Busuanga Island. It is part of the on-going<br />
detailed biostratigraphic study of the Island aimed at establishing<br />
<strong>radiolaria</strong>n biostratigraphy to provide basic paleontologic control in<br />
deciphering the tectonic setting of the area.<br />
Umeda, M. 1990. Jurassic <strong>radiolaria</strong>ns associated with<br />
chert arenite in the western part of the Nanjo Massif, Fukui<br />
Prefecture, central Japan. Bull. Fukui municip. Mus. nat.<br />
Hist., 37, 7-19. (in Japanese)<br />
Vishnevskaya, V.S. 1990. Albian-Cenomanian<br />
<strong>radiolaria</strong>ns from northwestern Pacific Regions, a tool for<br />
Paleotectonic reconstruction. In: Geology of the Pacific.<br />
Eds.), vol. 2. Dokl. Akad. Nauk SSR., pp. 3-16.<br />
Vishnevskaya, V.S., Agarkov, Y.V., Zakariadze,<br />
G.S. & Sedaeva, K.M. 1990. Late Jurassic-Cretaceous<br />
<strong>radiolaria</strong>ns of the Greater Caucasus as a key for determination<br />
of age and paleoenvironment of the ophiolites from the<br />
Lesser Caucasus. Dokl. Akad. Nauk SSSR, 310/6, 1417.<br />
Wakamatsu, H., Sugiyama, K. & Furutani, H.<br />
1990. Silurian and Devonian <strong>radiolaria</strong>ns from the<br />
Kurosegawa Tectonic Zone, southwest Japan. J. Earth Sci.<br />
Nagoya Univ., 37, 157-192.<br />
Well-preserved <strong>radiolaria</strong>ns are obtained from the Silurian and<br />
Devonian rocks of the Kurosegawa Tectonic Zone, Southwest Japan.<br />
On the basis of the existence of characteristic species, six<br />
assemblages are recognized. They are, the Secuicollacta ? exquisita<br />
assemblage (S. ? exquisita n. sp., S. ? sp. A, Goodbodium sp.,<br />
Palaeoscenidium spp., etc.; late Llandoverian-Wenlockian), the<br />
Pseudospongoprunum tazukawaensis assemblage (P. tazukawaensis<br />
n. gen., n. sp., Secucollacta ? sp., Spumellaria gen. indet. spp., etc.;<br />
middle Wenlockian-middle Ludlovian), the Pseudospongoprunum<br />
sagittaturn assemblage (P. sagittatum n. gen., n. sp., P. ? sp.,<br />
Haplentactinia sp., etc.; age unknown), the Devoniglansus unicus<br />
assemblage (D. unicus n. gen., n. sp., Copicyntra ? nuda n. sp.,<br />
Helioentactinia ? prismspinosa n. sp., etc.; age and the stratigraphic<br />
relationship to the P. sagittaturn assemblage unknown), the<br />
Palaeoscenidium ishigai assemblage (P. ishigai n. sp., Deflantrica<br />
solidum n. gen., n. sp., Ceratoikiscum Iyratum, etc.; Middle Devonian)<br />
and the Tlecerina-Glanta assemblage (T. horrida, T. exilis, G. fragilis<br />
n. gen., n. sp., Pactarentinia holdsworthi, Helenifore sp., etc.; Middle<br />
Devonian), in ascending order. Component species of these<br />
assemblages are fairly different from those of previously known<br />
Silurian and Devonian faunas of other districts, which may be caused<br />
by the difference of age and/or paleoenvironment.<br />
Four new genera, Deflantrica, Pseudospongoprunum,<br />
Devoniglansus and Glanta, are proposed and eleven new species and<br />
seventeen indeterminable species are described.<br />
Watanabe, Y., Asano, H., Ino, M., Kitamura, E.,<br />
Takahashi, O., Mashiko, S., Miyachi, T. &<br />
Ishii, A. 1990. Occurrence of Late Cretaceous fossils from<br />
the Tochiya Formation, northeastern part of the Kanto<br />
Mountains, central Japan. J. geol. Soc. Japan, 96/8, 683-<br />
685. (in Japanese)<br />
Welling, L.A. 1990. Radiolarian microfauna in the<br />
Northern California current system: spatial and temporal<br />
variability and implications for paleoceanographic<br />
- 57 -<br />
reconstructions. M. Sci. Thesis. Oregon State University,<br />
Corvallis, Oregon, 80 p. (unpublished)<br />
Yamashita, M. & Ishiga, H. 1990. Correlation<br />
between the <strong>radiolaria</strong>n and the fusulinacean biostratigraphy<br />
of the Upper Middle Permian in Atetsu Plateau, Okayama<br />
Prefecture, Southwest Japan. J. geol. Soc. Japan, 96, 687-<br />
689. (in Japanese)<br />
Yang, Q. & Wang, Y.J. 1990. A taxonomic study of<br />
Upper Jurassic <strong>radiolaria</strong>n from Rutog county, Xizang (Tibet).<br />
Acta micropalaeont. sinica, 7/3, 195-218.<br />
A diversified <strong>radiolaria</strong>n fauna from a chert sample of a<br />
primarily basic volcanic succession, locally known as the<br />
"Muggarkangri Group", in Rutog County, NW Xizang (Tibet), contains<br />
15 families, 32 genera, and 54 species-level taxa. One new family<br />
(Leugeonidae), three new genera (Dantze, Leugeo, and Levileugeo),<br />
and 12 new species are erected herein. This <strong>radiolaria</strong>n assemblage<br />
is assignable to Upper Kimmeridgian/Lower Tithonian (Subzone 2<br />
alpha to Subzone 3 beta of Pessagno et al., 1987b)~ based on the<br />
presence of Mirifusus guadalupensis, Tripocyclia jonesi, Hsuum<br />
maxwelli, etc.<br />
Yao, A. 1990. Triassic and Jurassic <strong>radiolaria</strong>ns. In: Pre-<br />
Cretaceous Terranes of Japan. Publication of IGCP Project<br />
No. 224: Pre-Jurassic Evolution of Eastern Asia. (Ichikawa,<br />
K., Mizutani, S., Hara, I., Hada, S. & Yao, A., Eds.). IGCP<br />
Project 224, Osaka, Japan. pp. 329-345.<br />
Triassic and Jurassic <strong>radiolaria</strong>ns are abundantly contained in<br />
siliceous and fine-grained clastic rocks of the Mesozoic sedimentary<br />
complexes of the B terrane-group (Ichikawa et al., 1985) that is the<br />
Jurassic-earliest Cretaceous terranes. Research on these<br />
<strong>radiolaria</strong>ns has recently played an important role in reexamination<br />
of "Upper Paleozoic" and Mesozoic stratigraphy and tectonic history<br />
of Japan. As important results, it is revealed that the B terranegroup<br />
is composed mainly of Mesozoic sedimentary complexes which<br />
for a long time were believed to be the Upper Paleozoic, and that the<br />
complexes are mostly the product of tectonic and/or sedimentary<br />
mixture of rocks of different ages. Moreover, it is clarified that the<br />
complexes are generally classified into three kinds of sequences,<br />
namely chert-clastics sequence, olistostromal sequence and clastic<br />
orderly sequence as cover sediments (cf. Matsuoka and Yao, in this<br />
book).<br />
In this paper, the author firstly reviews the brief history of<br />
Triassic and Jurassic <strong>radiolaria</strong>n researches in Japan, secondly<br />
summarizes the recent results on the <strong>radiolaria</strong>n biostratigraphy,<br />
thirdly correlates the Japanese zones with foreign ones, and finally<br />
remarks on the Triassic and Jurassic <strong>radiolaria</strong>n paleobiogeography.<br />
Yeh, K.Y. 1990. Taxonomic studies of Triassic Radiolaria<br />
from Busuanga Island, Philippines. Bull. natl. Mus. nat. Sci.,<br />
Taiwan, 2, 1-63.<br />
Bedded chert in Busuanga Island often contains abundant and<br />
highly diversified Radiolaria. This report deals with taxonomic<br />
studies of Middle and Upper Triassic Radiolaria from a bedded chert<br />
section near San Nicolas, Busuanga Island, Philippines. Three<br />
<strong>radiolaria</strong>n assemblages can be distinguished from the studied<br />
samples. These assemblages are Ladinian Busuanga chengi<br />
Assemblage, Carnian Trialatus megacornutus Assemblage, and upper<br />
Norian Livarella sp. A Assemblage. In this study over one hundred<br />
and fifty <strong>radiolaria</strong>n forms are figured, two new genera and fifteen<br />
new species are described.<br />
Yeh, K.Y. & Nien, C.Y. 1990. Radiolaria in surface<br />
sediments from marginal basin off southwest Taiwan. Bull.<br />
natl. Mus. nat. Sci., Taiwan, 2, 65-87.<br />
Radiolarian faunas were analyzed for the surface sediments<br />
from the basin to the southwest of Taiwan. In this study, the<br />
occurrence of <strong>radiolaria</strong>n faunas shows that 1) Radiolaria occurs<br />
from shallow coastal environment to the deep area; 2) the<br />
abundance and diversity of Radiolaria in the sediments are mainly<br />
controlled by the depth; the diversity of <strong>radiolaria</strong>n assemblage<br />
increases with increasing depth. Radiolarian assemblages in the<br />
sediments may indicate the variation of water masses of past. A<br />
preliminary test shows that during the deposition of these surface<br />
sediments, the water column of deep area consisted of at least three<br />
water masses; the boundaries of upper three water masses were<br />
possibly around the depths at 130 and 300 meters, respectively.
Bibliography - 1991 Radiolaria 14<br />
Abelmann, A. & Gersonde, R. 1991. Biosiliceous<br />
particle flux in the Southern Ocean. Marine Chem., 35, 503-<br />
538.<br />
The flux of diatom valves and <strong>radiolaria</strong>n shells obtained during<br />
short-term and annual sediment trap experiments at seven localities<br />
in the Atlantic sector of the Antarctic Ocean (in the Drake Passage,<br />
Bransfield Strait, Powell Basin, NW and SE Weddell Sea and the Polar<br />
Front north of Bouvet Island) is summarized and discussed. The<br />
deployment of time-series sediment traps provided annual flux<br />
records between 1983 and 1990. The biosiliceous particle flux is<br />
characterized by significant seasonal and interannual variations.<br />
Flux pulses, accounting for 70-95% of the total annual flux, occur<br />
during austral summer, with a duration ranging between about 2 and<br />
9 weeks. The annual values of vertical diatom and <strong>radiolaria</strong>n flux<br />
range between 0.26xl0 9 and morethan 26xl0 9 valves m -2 and<br />
between 0.21x10 4 and 70x10 4 shells m -2 , respectively. Interannual<br />
differences in the particle flux range over a factor of 10. Grazers<br />
play an important role in controlling the quantity, timing and pattern<br />
of the vertical biosiliceous particle flux.<br />
The flux pattern of diatoms and <strong>radiolaria</strong>ns is similar at most<br />
of the sites investigated and shows a close relationship between the<br />
production of siliceous phytoplankton and proto-zooplankton. At<br />
some sites, however, the <strong>radiolaria</strong>n flux pattern indicates probably<br />
phytoplankton production which is not documented by direct signals<br />
in the trap record. During their transfer through the water column to<br />
the ocean floor, the composition of the biosiliceous panicles is<br />
altered mechanically (breakdown by grazing zooplankton) and by<br />
dissolution, which significantly affects especially diatoms and<br />
phaeodarians in the upper portion of the water column and at the<br />
sediment-water interface.<br />
Significant lateral transport of suspended biosiliceous particles<br />
was observed in the bottom water layer in regions adjacent to shelf<br />
areas (Bransfield Strait), and in the vicinity of topographic<br />
elevations (Maud Rise), indicating considerable redistribution of<br />
biogenic silica in these regions.<br />
Aguado, R., O'Dogherty, L., Rey, J. & Vera, J.A.<br />
1991. Turbiditas calcáreas del Cretácico al Norte de Vélez<br />
Blanco (Zona Subbética): bioestratigrafía y génesis. Rev.<br />
Soc. geol. España, 4/3-4, 271-304.<br />
A stratigraphic, sedimentological and biostratigraphic study<br />
(including foraminifers, nannoplankton and <strong>radiolaria</strong>ns) of the<br />
Cretaceous rocks to the north of Velez Blanco (Internal Subbetic)<br />
reveals considerable variations in the thickness, lithology and age of<br />
the materials in many of the sections. The lowest lithostratigraphic<br />
unit, the Carretero Formation (Upper Berriasian to upper Barremian),<br />
crops out only locally and its facies are clearly pelagic, composed by<br />
marls, marly limestones and limestones. The uppermost Barremian,<br />
Aptian and Albian materials of the Fardes Formation are also pelagic<br />
facies and in many places have intercalations of carbonate turbidite<br />
deposits, oolitic turbidites and breccias, which in some sectors can<br />
be quite thick. Notable among these turbidites is a megabed mainly<br />
made up of variously sized fragments of middle Jurassic, shallow<br />
marine limestones, redeposited in the basin during the uppermost<br />
Aptian, which are up to 60 meters in thickness in places and are<br />
interpreted as being turbidites related to a seismic event. Materials<br />
from the Cenomanian-Turonian-Coniacian-Santonian (p.p.) have been<br />
recognised in pelagic facies in two lithostratigraphic units, the<br />
Capas Blancas Formation and "Upper Cretaceous carbonate breccia"<br />
which interfinger laterally. The upper lithostratigraphic term, the<br />
Capas Rojas Formation (Santonian/upper Maastrichtian) onlaps over<br />
Jurassic rocks, which were previously exposed upon the sea bed, and<br />
fossilizes the scarps of old faults. Intercalations of calcareous<br />
turbidites appear from place to place within these lower Senonian<br />
pelagic rocks.<br />
The carbonate turbidites were deposited in small tectonic<br />
basins bounded by normal faults, mainly in halfgrabens. Sedimentary<br />
gravity flows were fed by submarine reliefs formed of both Jurassic<br />
and Cretaceous materials and the fault scarps surrounding them.<br />
They represent sedimentary bodies deposited releted to the<br />
paleofaults on an apron model, sometimes relatively thin<br />
(calcarenitic levels) and sometimes much thicker (calcareous<br />
breccias and the megabed). The turbidites beds formed mainly, or<br />
sometimes exclusively, of oolites coming from the destruction of the<br />
Camarena Formation (middle Jurassic) are of particular interest;<br />
these would have been well exposed on the sea bottom from whence<br />
the turbidity currents and mass-gravitational flows were fed.<br />
Aitchison, J., Hada, S. & Yoshikura, S. 1991.<br />
Kurosegawa terrane: disrupted remmants of a low latitude<br />
Paleozoic terrane accreted to SW Japan. J. Southeast Asian<br />
Earth Sc., 6/2, 83-92.<br />
The Kurosegawa terrane is an anomalous, disrupted,<br />
predominantly Paleozoic lithotectonic assemblage of convergent<br />
1991<br />
- 58 -<br />
continental margin affinity locaied between two Mesozoic terranes in<br />
SW Japan. On the basis of Silurian macrofossils in limestones and<br />
sparse Devonian plant fossils in overlying volcaniclastic sediments<br />
portions of the terrane were considered previously to represent a<br />
Silurian through Devonian sedimentary succession. Radiolarian data,<br />
together with sedimentological analysis, indicate the possibility that<br />
hiatuses may occur in this succession although their position<br />
remains indeterminate. Faunal, floral and paleomagnetic data<br />
indicate low latitude development during the Paleozoic, probably near<br />
the northern margins of Gondwana. Late Paleozoic oceanic crustal<br />
rocks are incorporated in a chaotic complex which crops out along<br />
the northern margin of the terrane. The chaotic rocks are interpreted<br />
to represent remnants of a subduction complex. Spatial relations of<br />
weakly-metamorphosed subduction complex rocks distributed along<br />
the northern side of the terrane and higher grade blueschist-bearing<br />
rocks to the south may indicate that during the Late Paleozoic to<br />
Early Mesozoic, subduction was south-directed along the northern<br />
margin of the Kurosegawa terrane. In the Jurassic, the Kurosegawa<br />
terrane underwent an oblique collision with Japan which was then part<br />
of Eurasia. Strike-slip faulting, associated with, and post-dating this<br />
collision resulted in dispersal of the Kurosegawa terrane into a<br />
narrow, discontinuous belt which transects the outer zone of SW<br />
Japan.<br />
Alder, V.A. & Boltovskoy, D. 1991. Microplanktonic<br />
distributional patterns west of the Antarctic Peninsula, with<br />
special emphasis on the tintinnids. Polar Biol., 11/2, 103-<br />
112.<br />
Microplankton was sampled with a centrifugal suction pump in<br />
the surface layer (approx. 9 m) of the Bellingshausen Sea and the<br />
Bransfield Strait in March 1987, and concentrated with a 26 µmmesh<br />
net. Bulk microplanktonic settling volumes were assessed<br />
silicoflagellates and large thecate dinoflagellates were counted, and<br />
tintinnids were counted and identified to species. Average (and<br />
maximum) values for the entire area surveyed were as follows,<br />
settling volume: 6.7 (43.3) ml/m 3 ; silicoflagellates: 674 (7777)<br />
ind./l, 0.57 (6.54) mg C/m 3 , dinoflagellates: 109 (1321) ind./l,<br />
1.40 (16.98) mg C/m 3 ; tintinnids: 52 (589) ind./l, 1.15 (9.87) mg<br />
C/m 3 . The three geographic zones defined objectively on the basis<br />
of tintinnid specific assemblagcs also differed sharply in their<br />
surface salinity, overall microplanktonic abundance and bulk settling<br />
volume. The Bransfield Strait, with lowest settling volume values<br />
(2.1 ml/m3) and cell concentrations, was characterized by the<br />
dominance of Cymalocylis affinis/convallaria. In waters around the<br />
tip of the Antarctic Peninsula microplanktonic settling volumes<br />
averaged 4.6 ml/m 3 , cell concentrations were intermediate, and<br />
79% of the tintinnids were represented by Codonellopsis balechi.<br />
The Bellingshausen Sea was characterized by the lowest salinities<br />
and the highest settling volumes (8.7 ml/m 3 ) and cell counts;<br />
Laackmanniella spp. and Cymalocylis drygalskii, f. typica dominated<br />
this area. Almost all biological variables were significantly<br />
intercorrelated, and showed strong and mostly significant negative<br />
correlations with surface salinity, yet relationships between<br />
enhanced standing stock and ice melt water were not obvious;<br />
rather, highest microplanktonic concentrations seemed to be due to<br />
ice-associated growth. Extremely high spatial correlations were<br />
found between the tintinnids and the dinoflagellates (r 2 : 0.941),<br />
suggesting the existence of close links between these two groups.<br />
Tintinnid species-specific assemblages show a coherent<br />
distributional pattern and well defined environment-related trends;<br />
most clearly diferentiated preferences are exhibited by<br />
Laackmanniella prolongata (closely associated with ice-covered<br />
areas), Cymalocylis affinis/convallaria (oligotrophic open-ocean<br />
waters), and Codonellopsis balechi (coastal regions).<br />
Amon, E.O. 1991. The correlation of polyfacial Coniacian<br />
deposits of Urals using foraminifers. In: Paleontology and<br />
correlation of polyprovincial and polyfacial deposits.<br />
Reports of 38th Session of All-Union Paleontologic<br />
Society, Novosibirik, 1992, Siberian Branch USSR Acad.<br />
Sci. Publ., pp. 8-10. (in Russian)<br />
Ando, H., Tsukamoto, H. & Saito, M. 1991.<br />
Permian <strong>radiolaria</strong>ns in the Mt Kinkazan Area, Gifu City,<br />
Central Japan. Bull. Mizunami Fossil Mus., 18, 101-106. (in<br />
Japanese)<br />
Middle and late Permian <strong>radiolaria</strong>ns occur in the "Toishi-type"<br />
shale and massive black shale that crop out in the Mt. Kinkazan<br />
area, Gifu City, central Japan. The <strong>radiolaria</strong>ns of the genus<br />
Follicucullus Ormiston and Babcock are most abundant, and F<br />
scholasticus morphotype II is the most common species. In some<br />
samples, F scholasticus morphotype II coexists with<br />
Pseudoaibaillella globosa,: Albaillella cf. Ievis and A. cf. excelsa The<br />
origin of this puzzling mixture is discussed.
Radiolaria 14 Bibliography - 1991<br />
Banakar, V.K., Gupta, S.M. & Padmavathi, V.K.<br />
1991. Abyssal sediment erosion in the central Indian Basin:<br />
evidence from radiochemical and <strong>radiolaria</strong>n studies. Marine<br />
Geol., 96/1-2, 167-173.<br />
Radiochemical analyses of three spade cores collected around<br />
78 o E between 10°S and 12°S from the abyssal depths in the Central<br />
Indian Basin yield an average accumulaIion rate of 2 mm/ka. The<br />
ratios of 230 Th flux in the sediments to its production rate in the<br />
overlying water column (Fa/Fp) are extremely low (~0.2). This fact,<br />
and the absence of Collosphaera invaginata (first appearance datum,<br />
150-200 ka), an index <strong>radiolaria</strong>n species of Neogene Radiolarian<br />
Zone 1, indicate intense erosion and lateral transport of younger<br />
sediments from this region.<br />
The radiochemical and <strong>radiolaria</strong>n biostratigraphic evidence for<br />
nearly 175 ka of erosion of the chronological record of the<br />
sediments in this region has been attributed to the effect of<br />
turbulent Antarctic Bottom Water entering the Central Indian Basin<br />
through the northern saddles of the Ninety East Ridge<br />
Banerjee, R. & Iyer, S.D. 1991. Biogenic influence on<br />
the growth of ferromanganese micronodules in the Central<br />
India Basin. Marine Geol., 97/3-4, 413-421.<br />
With increasing depth, the abundance of ferromanganese<br />
micro-nodules decreases as their size increases, and the surface<br />
texture changes from rough to smooth. Biological debris, including<br />
<strong>radiolaria</strong>n fragments, diatom tests and bacterial cells were found<br />
associated with the micronodules. Dissolution of biological debris<br />
with increasing core depth was evident. It appears that biological<br />
debris play an important role in the growth of the micronodules<br />
Bareille, G., Labracherie, M., Labeyrie, L.,<br />
Pichon, J.J. & Turon, J.L. 1991. Biogenic silica<br />
accumulation rate during the Holocene in the southeastern<br />
Indian Ocean. Marine Chem., 35, 537-551.<br />
Three box-core transects were selected in the southeastern<br />
Indian Ocean to establish the variability of biogenic silica<br />
accumulation rate in the main subsystems of the Southern Ocean.<br />
Cicladophora davisiana and ∂ 18 0 chronologies, previously calibrated<br />
by 14 C dates, and biogenic silica contents determined by X-ray<br />
diffraction analysis were used to calculate accumulation rates.<br />
Concurrently, a transfer function was used to quantify the silica loss<br />
during the biogenic particulate accumulation in the deep-sea<br />
sediments. The average rate of biogenic silica rain on the sea-floor,<br />
calculated from the accumulation rate and the amount of dissolved<br />
biogenic silica, ranges from less than 0.1 to 16 g opal cm -2 ka -1 .<br />
During the Holocene, biogenic silica has accumulated at the highest<br />
rates on the Southeast Ridge, south of the Polar Frontal Zone. To the<br />
north and south, the accumulation rate drops where summer sea<br />
surface temperatures are above 8°C or lower than 2 o C. Biogenic<br />
silica dissolution is maximum in marginal sea ice zone. Accumulation<br />
rates of biogenic silica can be a useful index to estimate changes of<br />
palaeoproductivity in the southeastern Indian Ocean, although there<br />
is no strict proportionality between accumulation and silica rain<br />
rates.<br />
Barron, J.A., Baldauf, J.G., Barrera, E., Caulet,<br />
J.P., Huber, B.T., Keating, B.H., Lazarus, D.,<br />
Sakai, H., Thierstein, H.R. & Wei, W. 1991.<br />
Biochronology and magnetostratigraphic synthesis of Leg<br />
119 sediments from the Kerguelen Plateau and Prydz Bay,<br />
Antarctica. In: Proceedings of the Ocean Drilling Program,<br />
Scientific Results. (Barron, J.A., Larsen, B. et al., Eds.), vol.<br />
119. College Station, TX (Ocean Drilling Program), pp.<br />
813-847.<br />
This paper summarizes the biostratigraphy and<br />
magnetostratigraphy of the 11 sites drilled on the Kerguelen Plateau<br />
and in Prydz Bay, Antarctica, during ODP Leg 119. Excellent<br />
magnetobiochronologic reference sections were obtained at deepwater<br />
Sites 745 and 746 (0-10 Ma) and at intermediate depth Site<br />
744 (0-39 Ma) on the southern Kerguelen Plateau. Site 738, an<br />
intermediate depth companion site for Site 744, contains a nearly<br />
complete lowermost Oligocene to Turonian carbonate section<br />
including a continuous sequence across the Cretaceous/Tertiary<br />
boundary. Northern Kerguelen Sites 736 and 737 (ca. 600 m water<br />
depth) constitute a composite middle Eocene to Quaternary<br />
reference section near the present-day Antarctic Polar Front.<br />
Biostratigraphic control is limited in Prydz Bay Sites 739-743.<br />
Glacial sequences cored on the continental shelf at Sites 739 and<br />
742 appear to form a composite record, possibly from the<br />
uppermost middle Eocene to the Quaternary; the entire upper<br />
Oligocene and most of the Miocene, however, are removed at an<br />
unconformity. Preglacial sediments at Site 741 contain Early<br />
Cretaceous pollen and spores, but the red beds cored at Site 740<br />
- 59 -<br />
are unfossiliferous. Poorly-fossiliferous glacial sediments of<br />
probable Quaternary age were sampled on the upper slope at Site<br />
743.<br />
A magnetobiochronologic time scale is presented for the Late<br />
Cretaceous and Cenozoic of the Southern Ocean based on previous<br />
studies and the results of Leg 119 studies.<br />
Basov, V.A. & Vishnevskaya, V.S. 1991. Upper<br />
Mesozoic stratigraphy of the Pacific Ocean. In: Circum-<br />
Pacific Council for Energy and Mineral Resources. Eds.).<br />
Nauka, Moscow. pp. 200. (in Russian)<br />
The book is dealing with the biostratigraphy of the Pacific Upper<br />
Mesozoic sedimentary cover. Subdivision and correlation of the<br />
Upper Mesozoic deposits within under-sea rises and deepwater<br />
basins were carried out by means of planktonic foraminifers and<br />
<strong>radiolaria</strong>ns. The history of sedimentation in the Pacific Ocean during<br />
the Late Mesozoic i5 discussed. The paleontological part contains<br />
the microphotographs of both planktonic Foraminifera and Radiolaria<br />
characteristic species and new species descriptions of the latter<br />
ones.<br />
Baumgartner, P.O., Jud, R., O'Dogherty, L.,<br />
Gorican, S., Marcucci, M. & Conti, M. 1991.<br />
Mesozoic <strong>radiolaria</strong>n occurrences in the Umbria-Marche<br />
Apennines. Field trip guide book of the 6th. Interrad<br />
Meeting, Florence, Italy, September 1991, 1-23 p.<br />
This field trip offers the opportunity to visit the Mesozoic<br />
pelagic sequences of the Umbria-Marche area (Fig. 1) and to<br />
examine Middle Jurassic to Late Cretaceous Tethyan <strong>radiolaria</strong>nbearing<br />
rocks. The main topics addressed during this field trip are: 1.<br />
distribution patterns of Jurassic siliceous and calcareous pelagic<br />
facies in a basin and swell setting and genetic interpretation of<br />
radiolarites. 2. The generalized onset of nannofossil limestones near<br />
the Jurassic/Cretaceous boundary: evolution of the biosphere,<br />
paleoceanographic and climatic change in Western Tethys during the<br />
Early Cretaceous. 3. Black shale and cyclic marl/limestone<br />
sedimentation during the middle Cretaceous: the role of radioiarians<br />
in explaining widespread anoxia and Milankovich-type sedimentary<br />
cycles.<br />
Bender, P., Braun, A. & Königshof, P. 1991.<br />
Radiolarien und Conodonten aus unterkarbonischen<br />
Kieselkalken und Kieselschiefern des nördlichen Rheinischen<br />
Schiefergebirges. Geologica et Paleontologica, 25, 87-97.<br />
Siliceous and fluoritized <strong>radiolaria</strong>ns have been obtained<br />
together with Conodonts in beds of siliceous limestones and shales<br />
in a rock sequence near Lermarhe (northern Rheinisches<br />
Schiefergebirse). A <strong>radiolaria</strong>n fauna from the Upper Albaillellaindensis-zone<br />
has been assigned to the upper part of the anchoralislatus-zone<br />
of the Conodont biostratigraphic scale. Radiolarian<br />
faunas of the Upper Albaillella-cartalla-zone belong at least to the<br />
Upper texanus zone, most probably to the bilineatus-zone in their<br />
greatest part. A redeposition of isolated skeletons of older forms as<br />
found in Conodont faunas of several beds has nor been observed in<br />
the co-occurring <strong>radiolaria</strong>ns. Radiolarian-bearing sequences of<br />
siliceous rocks with common interlayers of allodapic limestones<br />
belonging to the Upper Albaillella-cartalla-zone possess a least<br />
thickness of 10 m.<br />
Blome, C.D. & Nestell, M.K. 1991. Evolution of a<br />
Permo-Triassic sedimentary melange, Grindstone terrane,<br />
east-central Oregon. Geol. Soc. Amer., Bull., 103/10, 1280-<br />
1296.<br />
The Grindstone terrane in east-central Oregon is one of the few<br />
areas in western North America where large blocks of<br />
unmetamorphosed Devonian, Mississippian, and Permian limestones<br />
are intermixed with Permian and Lower Triassic <strong>radiolaria</strong>n chert and<br />
Pennsylvanian?, Permian, and Triassic volcaniclastic rocks. Although<br />
originally described as parts of a coherent succession, we interpret<br />
the Grindstone rocks to be a sedimentary melange composed of<br />
Paleozoic limestone slide and slump blocks that became detached<br />
from a carbonate shelf fringing a volcanic knoll or edifice in Late<br />
Permian to Middle Triassic time and were intermixed with Permian<br />
and Triassic slope to basinal clastic and volcaniclastic rocks in a<br />
forearc basin setting. Paleogeographic affinities of the Grindstone<br />
limestone faunas and volcaniclastic debris in the limestone and<br />
clastic rocks all indicate deposition in proximity to an island-arc<br />
system near the North American craton. The Grindstone terrane<br />
deposits are unconformably overlain by Upper Triassic to Middle<br />
Jurassic sequences of the Izee terrane. Although lithologic and<br />
faunal differences indicate that the Grindstone and Izee terranes<br />
together represent a tectonic block separate from the adjacent<br />
Baker terrane, all three terranes were juxtaposed by Late Triassic or<br />
Early Jurassic time.
Bibliography - 1991 Radiolaria 14<br />
We recommend reduction to informal status for the Coffee<br />
Creek (Mississippian), Spotted Ridge (Pennsylvanian?), and Coyote<br />
Butte (Permian) formations because (13 they cannot be mapped or<br />
traced beyond limited areas, and (2) these older rocks are<br />
chaotically intermixed with younger chert and volcaniclastic rocks.<br />
New biostratigraphic data indicate that the bulk of the Spotted Ridge<br />
volcaniclastic rocks represent a part of the Triassic Vester<br />
Formation of the Izee terrane.<br />
Boltovskoy, D. 1991. Holocene-upper Pleistocene<br />
<strong>radiolaria</strong>n biogeography and paleoecology of the Equatorial<br />
Pacific. Palaeogeogr. Palaeoclimatol. Palaeoecol., 86/3-4,<br />
227-241.<br />
Polycystine <strong>radiolaria</strong>ns were investigated in 66 samples from<br />
5 box-cores spanning the last ca. 40,000 years from the western<br />
(approx. 160°E) and the central (136°W) equatorial Pacific. The<br />
assemblages investigated show clear differences associated with<br />
the geographic locations of the sites: the central Pacific is<br />
characterized by higher specific diversities. much higher absolute<br />
abundances of shells per gram of dry bulk sediment, and by<br />
conspicuously better <strong>radiolaria</strong>n preservation. The differences<br />
involved also include significant changes in the relative proportions<br />
of several <strong>radiolaria</strong>n species (these accounting for approx. 25% of<br />
total individuals). families and orders. These dissimilarities are<br />
chiefly attributed to differences in the primary production of the two<br />
zones and to enhanced advection of colder-water species<br />
characteristic of the California Current to the central equatorial<br />
Pacific. In both areas, downcore faunal changes, if present at all, are<br />
so weak that background noise from random sample-to-sample<br />
variations almost completely masks them. There do not seem to be<br />
any noticeable shifts associated with the 18 k.y. B.P.level.<br />
Inconclusive evidences of environmental changes at 30-20 k.y. B.P.<br />
are suggested in some of the cores by the increase in the<br />
proportions of several species characteristic of colder northeastern<br />
Pacific waters and by lower <strong>radiolaria</strong>n accumulation rates; these<br />
changes seem to be paralleled by shifts in the isotopic composition<br />
of planktonic Foraminifera.<br />
Bragin, N.Y. 1991. Radiolaria and lower mesozoic units of<br />
the USSR East regions. Transactions, Nauka 469, 1-122 p.<br />
(in Russian)<br />
The stratigraphic distribution of microfauna in sequences has<br />
been analysed on the material of Sikhote-Alyn, Sakhalin and Koryak<br />
Upland. 7 zones and stratigraphic layers with <strong>radiolaria</strong>ns and 17<br />
zones and stratigraphic layers are established at Sikhote-Alyn in<br />
interval from the middle part of Lower Triassic to Triassic—Jurassic<br />
boundary. Several zones are traced at Sakhalin and Koryak Upland;<br />
the correlation with sequences of Mediterranean area, USA and<br />
Japan is realised. The development of <strong>radiolaria</strong>n assemblages in<br />
Triassic is studied. On the base of new stratigraphic data the idea of<br />
small thickness and, in opposite, great stratigraphic volume of chert<br />
units was formulated, then, the Triassic paleogeography of northeast<br />
Asia has been analysed, conditions of chert units formation<br />
were discussed and its paleooceanic origin has been supposed.<br />
Bragin, N.Y. 1991. Carnian <strong>radiolaria</strong>n complex of<br />
volcanogenic siliceous formations of the Ekonay zone in the<br />
Koryak Upland. Izv. Akad. Nauk SSSR, ser. geol., 6, 79-86.<br />
(in Russian)<br />
Consecutive complexes of <strong>radiolaria</strong>, ranging from Carnian to<br />
late Norian-Rhaetian (?), were discovered in the section from<br />
volcanogenic-siliceous formations on the river Podgornaya. They are<br />
similar to Radiolaria known in other regions in the east of the USSR.<br />
An exception is an association of late Carnian age with<br />
Capnuchosphaera deweveri etc. which is more similar to complexes<br />
from the Mediterranean and has as yet no clear analogues in the<br />
USSR. This association includes a new species, Bernoullius (?)<br />
capricornus sp. nov. which is described<br />
Bragina, L.G. 1991. Radiolarians from the Bystrinsk<br />
sequence Santonian-Campanian of northwest Kamchatka.<br />
Seriya Geologicheskaya, 7/7, 129-136. (in Russian)<br />
Braun, A. & Amon, E.O. 1991. Fluoritisierte<br />
Radiolarien aus Kieselkalk-Banken des Mittel-Viseum<br />
(Unterkarbon) des Rheinischen Schiefergebirges<br />
(Deutschland). Paläont. Z., 65/1-2, 25-33.<br />
From siliceous shales (Lower Carboniferous, Rheinisches<br />
Schiefergebirge), in direct neighborhood to a bed of allodapic<br />
limestone, the following fluoritized <strong>radiolaria</strong>n fauna has been<br />
extracted by chemical transformation of originally calcified<br />
skeletons: Albaillella cartalla, Latentifistula turgida, Eostylodictya<br />
cf. eccentrica, Tetragregnon sycamorensis sycamorensis, Belowea<br />
variabilis, Callela ? hexactinia, Entactinia tortispina and Entactinia<br />
- 60 -<br />
variospina. The limestone bed has been dated by calcareous<br />
foraminifera as being mid Visean in age (V 2b-3a, Cf 5-foraminiferal<br />
zone). The diagenetic calcification took place after the selective<br />
dissolution of the skeletons and was in itself not selective.<br />
Braun, A. & Gursky, H.J. 1991. Kieselige<br />
sedimentgesteine des unter-Karbons im Rhenoherzynikum -<br />
eine bestandsaufnahme. Geologica et Paleontologica, 25,<br />
57-77.<br />
Based on published and own data, the state-of-the-art of<br />
investigation on Lower Carboniferous siliceous-rock bearing<br />
sedimentary sequences in Central Europe is briefly reviewed.<br />
Regional occurrence, lithology, sedimentology, petrography, fossil<br />
content, and age are addressed. Four stratigraphic levels are mostly<br />
or partly represented by siliceous rocks in the northern and eastern<br />
Rheinisches Schiefergebirge, Kellerwald, Upper and northern Middle<br />
Harz areas:<br />
D) Siliceous Transitional Beds (Kieselige Übergangsschichten;<br />
cu Go α),<br />
C) Light-Coloured Cherts/Cherty Limestones (Helle/Bunte<br />
Kieselschiefer/ Kieselkalke; cu Pe ∂)<br />
B) Black Cherts (Schwarze Kieselschiefer/Lydite; cu Pe ß-γ),<br />
A) Lower Alum Shales (Liegende Alaunschiefer; cu ?Ga-Pe α).<br />
A correlation scheme of goniatite, conodont, foraminiferal and<br />
<strong>radiolaria</strong>n biostratigraphy of the Rhenohercynian Lower<br />
Carboniferous is presented. Partly Corg-rich ribbon cherts and slaty<br />
siliceous mudstones as well as metabentonites and fine- grained<br />
turbiditic limestones alternate to form the rhythmical bedding of the<br />
sequences. Laminations and diagenetical deformations of the<br />
bedding are characteristical. The siliceous rocks are mainly<br />
composed of quartz/chalcedony and very fine-grained siliciclastic<br />
detritus; <strong>radiolaria</strong>ns and sponge spiculae are abundant, but variably<br />
preserved. Recrystallization and pressure solution of different<br />
grades are typical. The metabentonite layers mainly consist of<br />
mixed-layer clay minerals and partly contain volcanogenic relics.<br />
SEM, X-ray diffractometry and chemical data complete the<br />
petrographic analyses. Detailed study of the <strong>radiolaria</strong>ns contributes<br />
to the interpretation of deposition, diagenesis and ecology of the<br />
original sediments. The discussion on the origin and the<br />
paleogeography are sketched.<br />
Carter, E.S. 1991. Late Triassic <strong>radiolaria</strong>n<br />
biostratigraphy of the Kunga Group, Queen Charlotte Islands,<br />
British Columbia. In: Evolution and Hydrocarbon Potential<br />
of the Queen Charlotte Basin, British Columbia. Eds.), vol.<br />
90-10. Geological Survey of Canada, Paper, pp. 195-201.<br />
Diverse, well preserved Upper Carnian and Norian <strong>radiolaria</strong>ns<br />
are present in the Peril and Sandilands formations of the Kunga<br />
Group, Queen Charlotte Islands. Ammonoids, bivalves, and conodonts<br />
are associated with most <strong>radiolaria</strong>n assemblages. The oldest f<br />
faunas are Late Carnian and occur with ammonoids from the Lower<br />
Welleri Zone. Capnodoce De Wever is rare in these assemblages but<br />
becomes more abundant and diverse in uppermost Carnian ones.<br />
Described <strong>radiolaria</strong>n species from eastern Oregon, western Europe,<br />
and the Mediterranean area are present in all samples, but the<br />
majority of taxa (particularly Upper Carnian) are new.<br />
Capnodoce fragilis Blome, Harsa siscwaiensis n. gen. n. sp., and<br />
Xiphosphaera fistulata n. sp. are abundant in upper Lower Norian to<br />
lower Middle Norian strata of the Queen Charlotte Islands. This<br />
three-fold <strong>radiolaria</strong>n association is a useful marker for this interval<br />
of time; it has not been found in older or younger assemblages. Two<br />
new species and one new genus are described in this report.<br />
Upper Norian <strong>radiolaria</strong>ns of the Betraccium deweveri Subzone<br />
are present in the Monotis beds of the uppermost Peril Formation.<br />
Three informal Upper Norian <strong>radiolaria</strong>n assemblages have been<br />
proposed for post- Monotis strata of the overlying Sandilands<br />
Formation.<br />
Carter, E.S. & Jakobs, G.K. 1991. New aalenian<br />
Radiolaria from the Queen Charlotte Islands, British<br />
Columbia: implications for biostratigraphic correlation.<br />
Geol. Surv. Canada, curr. res., Pap., 91-1A, 337-351.<br />
This is a preliminary report on diverse, well preserved Aalenian<br />
<strong>radiolaria</strong>ns that have been found in a carbonate concretion from the<br />
belemnite sandstone member of the Phantom Creek Formation on the<br />
Yakoun River, Queen Charlotte Islands. The sample is associated with<br />
an Aalenian ammonite fauna that is previously unknown from this<br />
area and indicates a probable early late Aalenian age for the<br />
<strong>radiolaria</strong>n sample. This faunal association extends the range of<br />
known Toarcian and Aalenian <strong>radiolaria</strong>ns, documents the presence<br />
of widely known taxa from other areas whose age may be equivalent
Radiolaria 14 Bibliography - 1991<br />
to the Queen Charlotte Islands taxa, and illustrates some new forms.<br />
One ammonite and J7 <strong>radiolaria</strong>n species are illustrated.<br />
Catalano, R., Di Stefano, P. & Kozur, H. 1991.<br />
Permian circumpacific deep-water faunas from the western<br />
Tethys (Sicily, Italy) - new evidences for the position of the<br />
Permian Tethys. Palaeogeogr. Palaeoclimatol. Palaeoecol.,<br />
87/1-4, 75-108.<br />
Circumpacific deep-water faunas, characterized mainly by<br />
<strong>radiolaria</strong>ns, paleopsychrospheric ostracods and conodonts, were<br />
found in the early, middle and late Permian deposits pertaining to the<br />
Sicanian paleogeographic domain of western Sicily, near the western<br />
end of the Eurasiatic Tethys. Similar Permian deep-water faunas are<br />
known from the Phyllite Unit of Crete and from Oman in the latter<br />
area partly above oceanic crust. All these occurrences indicate the<br />
presence of a late Paleozoic Tethys ocean immediately north of<br />
Gondwana.<br />
Caulet, J.P. 1991. Radiolarians from the Kerguelen<br />
Plateau, Leg 119. In: Proceedings of the Ocean Drilling<br />
Program, Scientific Results. (Barron, J., Larsen, B. et al.,<br />
Eds.), vol. 119. College Station, TX (Ocean Drilling<br />
Program), pp. 513-546.<br />
Radiolarians are abundant and well preserved in the Neogene of<br />
the Kerguelen Plateau. They are common and moderately to well<br />
preserved in the Oligocene sequences of Site 738, where the<br />
Eocene/Oligocene boundary was observed for the first time in<br />
subantarctic sediments, and Site 744. Radiolarians are absent from<br />
all glacial sediments from Prydz Bay.<br />
Classical Neogene stratigraphic markers were tabulated at all<br />
sites. Correlations with paleomagnetic ages were made at Sites 745<br />
and 746 for 26 Pliocene-Pleistocene <strong>radiolaria</strong>n events. Many<br />
Miocene to Holocene species are missing from Sites 736 and 737,<br />
which were drilled in shallow water (less than 800 m). The missing<br />
species are considered to be deep-living forms.<br />
Occurrences and relative abundances of morphotypes at six<br />
sites are reported. Two new genera (Eurystomoskevos and<br />
Cymaetron) and 17 new species (Actinomma kerguelenensis, A.<br />
campilacantha, Prunopyle trypopyrena, Stylodictya tainemplekta,<br />
Lithomelissa cheni, L. dupliphysa, Lophophaena(?) thaumasia,<br />
Pseudodictyophimus galeatus, Lamprocyclas inexpectata, L.<br />
prionotocodon, Botryostrobus kerguelensis, B. rednosus, Dictyoprora<br />
physothorax, Eucyrtidium antiquum, E.(?) mariae, Eurystomoskevos<br />
petrushevskaae, and Cymaetron sinolampas) are described from the<br />
middle Eocene to Oligocene sediments at Sites 738 and 744.<br />
Twenty-seven stratigraphic events are recorded in the middle to late<br />
Eocene of Site 738, and 27 additional stratigraphic datums are<br />
recorded, and correlated to paleomagnetic stratigraphy, in the early<br />
Oligocene at Sites 738 and 744. Eight <strong>radiolaria</strong>n events are<br />
recorded in the late Oligocene at Site 744.<br />
New evolutionary lineages are proposed for Calocyclas<br />
semipolita and Prunopyle trypopyrena.<br />
Conti, M. & Marcucci, M. 1991. Radiolarian<br />
assemblage in the Monte Alpe cherts at Ponte di Lagoscuro,<br />
Val Graveglia (eastern Liguria, Italy). Eclogae geol. Helv.,<br />
84/3, 791-817.<br />
The Jurassic formation of Monte Alpe Cherts is the lowest unit<br />
in the sedimentary cover of ophiolites and ophiolite breccias in the<br />
Northern Apennines. A section of this formation has been studied at<br />
Ponte di Lagoscuro, Val Graveglia (Liguria), and an exceptionally rich<br />
<strong>radiolaria</strong>n assemblage of middle Callovian age has been isolated<br />
from chert nodules in its lower part. Several new species are<br />
described in this assemblage<br />
Csontos, L., Dosztály, L. & Pelikán, P. 1991.<br />
Radiolarians from the Bükk Mts. M. All. Földtani Intézet évi<br />
jelentése, 357-381. (in Hungarian)<br />
We investigated radiolarite samples from the Bükk Mts, NE<br />
Hungary. About one third of the samples yielded <strong>radiolaria</strong>ns of some<br />
stratigraphic value. The highly silicified samples were macerated<br />
with 4—6% hydrogene fluoride. The fossils were poorly preserved<br />
because of silicification and deformation. However, they gave much<br />
needed information about the different stratigraphic levels of the<br />
two major structural units of the Bükk Mountains.<br />
The stratigraphy of the Bükk Autochtonous has become more<br />
detailed by the <strong>radiolaria</strong>n finds in the borehole Felsotárkány 7. The<br />
black radiolarite is accompanied here by acid volcanites, members of<br />
the Aniso—Ladinian volcanic suite (Szent István-hegy Porphyry). The<br />
<strong>radiolaria</strong>ns gave Ladinian age.<br />
- 61 -<br />
In the higher stratigraphic levels of the Autochtonous mostly<br />
red radiolarites occur in two close horizons: the first between the<br />
diverse Triassic limestones and the black shales, and the second<br />
within the black shales, very close to their base. The <strong>radiolaria</strong>ns<br />
from the practically continuous lower horizon (samples Nos 8, 9, 10,<br />
11, 12, 18, 19, 20, 21, 22, 26) and from the lenses within the<br />
black shale (3, 13, 14, 15) indicated the same age: the boundary<br />
between the Middle and Upper Jurassic, more precisely a Callovian—<br />
Oxfordian age.<br />
The strata of the Mónosbél—Szarvasko' nappes yielded<br />
radiolarite lenses and layers from different parts of the proposed<br />
stratigraphic column. Since the sediments of these nappes are the<br />
result of intense reworking, the obtained ages are to be used with<br />
great care.<br />
Samples of the radiolarite lenses coming from the Western<br />
Bükk area, from the close vicinity of the Szarvasko—type mafic<br />
bodies (samples No 1, 2, 5) indicate Middle Jurassic or younger<br />
ages. The layered black radiolarites found supposedly over this<br />
stratigraphic level (4, 6, 7) show a Callovian—Oxfordian age.<br />
The other samples are derived from the same nappe units but<br />
from the Southeastern Bükk area. The radiolarite lens found in a<br />
shale containing also limestone lenses yielded fossils of Bathonian—<br />
Callovian age. The thick black chert (layered radiolarite and/or<br />
sedimentary radiolarite breccia; samples No 24, 25) covering the<br />
Bükkzsérc allodapic oolithic limestone of Late Dogger—Early<br />
Malmian age, gave <strong>radiolaria</strong>ns of the same age.<br />
We have a problematic sample (23) taken from an allodapic<br />
limestone bed previously supposed to be of Late Liassic age, based<br />
on foram finds. This black chert nodule gave badly preserved<br />
<strong>radiolaria</strong>ns of Late Jurassic age. If this age is ascertained by<br />
further work, we have to reevaluate the significance of the<br />
foraminiferal ages and the model stratigraphic column of the<br />
Mónosbél—Szarvasko nappes.<br />
The recent <strong>radiolaria</strong>n finds and works of MATSUOKA and YAO<br />
(1986) and of AITA (1987) enable us to revaluate the stratigraphic<br />
position of the Unuma echinatus zone. The fossils previously<br />
described from the Bükk mountains (KOZUR 1984) belong to the<br />
Tricolocapsa plicarum (= Ununa echinatus) zone, but unlike KOZUR<br />
(1984), GRILL and KOZUR (1986), we think that the age of the zone<br />
is Bathonian—Callovian. This stratigraphic position corresponds<br />
much better to the reevaluated position of the zone by AITA (1987)<br />
and to the fossils found now.<br />
De Master, D.J., Nelson, T.M., Harden, S.L. &<br />
Nittrouer, C.A. 1991. The cycling and accumulation of<br />
biogenic silica and organic carbon in Antarctic deep-sea and<br />
continental margin environments. Marine Chem., 35, 489-<br />
502.<br />
Rates of biogenic silica and organic carbon accumulation are<br />
reported for Antarctic deep-sea and continental margin deposits.<br />
Naturally occurring radionuclides ( 226 Ra, 231 Pa, and 230 Th) were<br />
used to establish rates of sediment accumulation in the rapidly<br />
accumulating siliceous deposits beneath the Antarctic Polar Front.<br />
The rates were as high as 20-180 cm ka -1 , and when coupled with<br />
biogenic silica and organic carbon measurements, yield accumulation<br />
rates as high as 35 mg cm -2 year -1 for silica and 0.3 mg cm -2 year -1<br />
for organic carbon. SiO2 /organic C weight ratios in Polar Front<br />
sediments are typically about 100, although values as high as 300<br />
were measured. Considering that the SiO2 /organic C ratio in Polar<br />
Front plankton ranges from 0.5 to 2, the high ratios observed in<br />
Polar Front sediments indicate that during settling and burial an<br />
enrichment of 50-600-fold occurs in biogenic silica relative to<br />
organic carbon.<br />
Rates of sediment accumulation were determined for the<br />
continental margin deposits of the Bransfield Strait and the Ross Sea<br />
using 210 Pb and 14 C chronologies. Accumulation rates ranged from<br />
0.02 to 0.5 cm year -1 . Based on these data and measurements of<br />
biogenic silica and organic carbon content, typical rates of<br />
accumulation on the continental margin are of the order of 3-12 mg<br />
cm -2 year -1 for silica and 0.1-0.8 mg cm -2 year -1 for organic carbon.<br />
The SiO 2 /organic C weight ratios in these continental margin<br />
sediments range from 3 to 32. Comparing the accumulation rate<br />
data with estimates of annual silica and organic carbon production<br />
rates indicates that approximately 25-50% of the gross silica<br />
production in surface waters is preserved in the sea-bed, in contrast<br />
to less than 5% of the organic carbon. In some of the continental<br />
margin environments, lateral transport of biogenic material can<br />
create local areas where the rate of silica accumulation is equal to<br />
as much as 70% of the production in the overlying water column. In<br />
the Southern Ocean environments examined in this study, biogenic<br />
silica is preferentially preserved in the sedimentary record relative<br />
to organic carbon. This trend is consistent with the greater role of<br />
Southern Ocean deposits in the global silica cycle as compared with<br />
the organic carbon cycle.
Bibliography - 1991 Radiolaria 14<br />
Dosztály, L. 1991. Triassic <strong>radiolaria</strong>ns from the Balaton<br />
upland. M. All. Földtani Intézet évi jelentése, 333-355. (in<br />
Hungarian)<br />
The Triassic formations in the Balaton Upland contain<br />
<strong>radiolaria</strong>ns in several areas and beds (Fig. 1). The richest faunas<br />
are dated as Late Anisian, Ladinian or Early Carnian. In the area<br />
concerned a large amount of volcanic material was introduced into<br />
the sea during the Middle Triassic. This caused the dissolved silica<br />
content of sea water to have increased offering favourable<br />
conditions for the propagation of <strong>radiolaria</strong>ns. The favourable living<br />
conditions resulted, from time to time, in a sudden increase in the<br />
number of <strong>radiolaria</strong>n taxa. Normally, a two-third of the species was<br />
changed during the span of time represented by a substage. In the<br />
region the sedimentation took place in a relatively shallow (not<br />
deeper than 200 metres) environment. Radiolarian-bearing deposits<br />
had largely been mingled with relatively large amounts of carbonate<br />
and volcanic materials. This is the main influencing factor of having<br />
found in general, only a few beds in which rich and well-preserved<br />
fauna can be encountered. The second reason is represented by<br />
dispersal silica that has prevented <strong>radiolaria</strong>ns from being dissolved<br />
out from the rocks. For each locality, a detailed description will be<br />
given only for the beds containing the richest fauna.<br />
New taxa: Pterospongus aquila n. sp.; Baumgartneria dumitricae<br />
n. sp.; Muelleritortis hungarica n. ssp. Muelleritortis nobilis n. sp.;<br />
Annulosaturnalis trispinosus n. gen. n. sp.<br />
Dumitrica, P. 1991a. Cenozoic Pyloniacea (Radiolaria)<br />
with a five-gated microsphere. Rev. Micropaléont., 34/1, 35-<br />
56.<br />
A new type of microsphere, characterized by the presence of<br />
five gates and derived from hypothetical prism is described. It is<br />
considered as representing the fifth fundamental type of<br />
pyloniacean microsphere. Three variants of such a microsphere<br />
characterizing three genera, are illustrated and described in detail,<br />
and their structural unity is emphasized. Two new genera<br />
(Pentapylonium and Trimanicula) and three new species<br />
(Pentapylonium implicatum ,Trimanicula centrospina and T.<br />
penultima) are described. The mode of growth of their skeleton,<br />
which is of pyloniacean type, is analysed in detail.<br />
Dumitrica, P. 1991b. Middle Triassic Tripedurnulidae, n.<br />
fam. (Radiolaria) from the eastern Carpathians (Romania) and<br />
Vicentinian Alps (Italy). Rev. Micropaléont., 34/4, 261-<br />
278.<br />
The new family Tripedurnulidae. with 4 genera (of which 3 are<br />
new) and 14 species (of which 13 are new), is described from<br />
Pelsonian limestones of the Eastern Carpathians (Romania) and<br />
upper Illyrian-Fassanian limestones of the Vicentinian Alps (Italy)<br />
and Eastern Carpathians (Romania). Terminology and orientation of<br />
nassellarian initial skeleton are discussed, and revised terminology<br />
is proposed.<br />
Dumitrica, P. & De Wever, P. 1991. Assignation to<br />
<strong>radiolaria</strong> of two Upper Jurassic species previously described<br />
as Foraminifera: systematic consequences. C.R. Acad. Sci.<br />
(Paris), Sér. II, 312, 553-558.<br />
Two species described in 1867 by Karrer as foraminifera<br />
(Lagena dianae Karrer and Orbulina neojurensis Karrer) from the<br />
Oxfordian cherty limestones near Vienna (Austria) are in all<br />
probability Radiolaria. This fact has both systematical and historical<br />
consequences: (a) Lagena dianae becomes a senior synonym of<br />
Mirifusus mediodilatatus (Rüst), a common and characteristic<br />
species of the Upper Jurassic, and has priority over this name and<br />
over all the other synonyms of this species, (b) F. Karrer and not<br />
Zittel should be considered as the first who described pre-Tertiary<br />
<strong>radiolaria</strong>ns.<br />
El Kadiri, K. 1991. La Dorsale Calcaire (Rif interne,<br />
Maroc): stratigraphie, sédimentologie et évolution<br />
géodynamique d'une marge alpine durant le Mésozoïque. Mise<br />
en évidence d'un modèle. Ph.D. Thesis. University of<br />
Tétouan, 355 p. (unpublished)<br />
Elbrächter, M. 1991. Faeces production by<br />
dinoflagellates and other small flagellates. Marine Microbial<br />
Food Webs, 5/2, 189-204.<br />
Faecal production by protists and particularly by flagellates has<br />
been more or less neglected so far in ecosystem research. Faeces<br />
production is documented here for photosynthetic and obligate<br />
heterotrophic dinoflagellates and <strong>radiolaria</strong>ns. Food uptake is also<br />
known from other phototrophic and heterotrophic small flagellates<br />
which are quite abundant in aquatic environments. Potential faeces<br />
- 62 -<br />
production of these flagellates are calculated. The role these<br />
particles may play in the environment is discussed.<br />
Faure, M., Iwasaki, M., Ichikawa, K. & Yao, A.<br />
1991. The significance of Upper Jurassic <strong>radiolaria</strong>ns in high<br />
pressure metamorphic rocks of SW Japan. J. Southeast Asian<br />
Earth Sc., 6/2, 131-136.<br />
Upper Jurassic <strong>radiolaria</strong>n remains have been discovered for<br />
the first time in pelitic rocks from the domain affected by<br />
Sanbagawa metamorphism, in Eastern Shikoku. As pod similar<br />
lithological successions and structures are observed from E. Kyushu<br />
to the Kanto Mountains, over a 800 km length, the age<br />
determination from Eastern Shikoku is significant for the whole belt.<br />
Firstly the available biostratigraphic data for the metamorphic<br />
domain are reviewed and the depositional age of the upper part of<br />
the metamorphic domain is determined. Secondly, stratigraphic<br />
evidence is added to the structural evidence for the thrusting of a<br />
middle Jurassic nappe (the Superficial nappe) upon the metamorphic<br />
domain.<br />
Fourcade, E., Dercourt, J., Gunay, Y., Azema, J.,<br />
Kozlu, H., Bellier, J.P., Cordey, F., Cros, P., De<br />
Wever, P., Enay, R., Hernandez, J., Lauer, J.P. &<br />
Vrielynck, B. 1991. Stratigraphie et paléogéographie de<br />
la marge septentrionale de la plate-forme arabe au Mésozoique<br />
(Turquie du Sud-Est). Bull. Soc. géol. France, 162/1, 27-41.<br />
In southeastern Turkey, the distal margin of the Arabian<br />
platform is overthrust by the Hezan allochthonous units consisting<br />
of Liassic sediments of inner carbonate platform origin and of thin<br />
Bathonian to Maastrichtian deep-water deposits. The pelagic<br />
sequence is interrupted by numerous hiatuses and punctuated by<br />
intercalated turbidites. These stable margin units are overthrust by<br />
ophiolites. Triassic tholeiitic pillow lavas of MORB type discovered<br />
for the first time in southeastern Turkey, and by Triassic to<br />
Hauterivian radiolarites belonging to the Koçali Unit. These<br />
radiolarites are derived from a Mesozoic through bordered to the<br />
south by the Arabian platform. The Koçali Unit documents the<br />
longevity of radiolarite deposition in this art of the Tethys.<br />
Garrison, D.L. 1991. An overview of the abundance and<br />
role of protozooplankton in Antarctic waters. J. Marine<br />
Syst., 2, 317-331.<br />
The classic view of the Antarctic pelagic system has suggested<br />
that food web dynamics are dominated by the diatom-krill food web<br />
link. Recent observations, however, have indicated that this is an<br />
oversimplification and that the antarctic food web has a complexity<br />
similar to that found in lower latitude systems. More specifically,<br />
small particulate feeding protozoans appear to have a much greater<br />
importance than was previously assumed.<br />
Only a few studies have been sufficiently extensive to<br />
characterize the Antarctic pelagic protozoan assemblage. These<br />
indicate that heterotrophic flagellates (dinoflagellates and other<br />
heterotrophic nannoplankton and ciliates (mostly non-loricate<br />
oligotrichs) dominate the protozooplankton assemblages in surface<br />
waters. The combined biomass of protozooplankton has been<br />
reported to comprise from c 7 to > 75% of the total nanno- and<br />
microplankton biomass depending on season and location.<br />
Protozoans are also found in sea ice communities where their<br />
abundances exceed those typically found in the plankton. Several<br />
prolozoan species DCCUpy bolh ice and water habitals, suggesting<br />
Ihal seasonally melling sea ice may be Ihe source of ice-edge<br />
prolozooplankton assemblages.<br />
The feeding rates of protozooplankton in Antarctic waters are<br />
poorly documented. Consumption estimates on clearance rates and<br />
some preliminary grazing experiments, however, indicate that the<br />
protozooplankton should be capable of utilizing a significant<br />
proportion of the daily primary and bacterioplankton production.<br />
Protozoans may contribute to vertical flux, but present evidence<br />
suggests that their contribution will be lower than from other<br />
sources.<br />
Garrison, D.L., Buck, K.R. & Gowing, M.M.<br />
1991. Plankton assemblage in the ice edge zone of the<br />
Weddell Sea during the austral winter. J. Marine Syst., 2,<br />
123-130.<br />
Plankton studies in Antarctic waters have emphasized the<br />
importance of diatoms. The species composition, abundances and<br />
contribution to biomass of the other planktonic groups are still<br />
poorly documented. This is particularly true for the heterotrophic<br />
members of the nano- and microplankton assemblage. As part of the<br />
Antarctic Marine Ecosystem Research in the Ice age Zone (AMERIEZ)<br />
program, we sampled nano- and microplankton across the ice edge<br />
zone during the austral winter. A variety of microscopical techniques
Radiolaria 14 Bibliography - 1991<br />
allowed us to the composition, trophic mode and biomass of the<br />
spectrum of organisms that make up the winter plankton<br />
assemblage.<br />
Total nano- and microplankton biomass in the upper 100<br />
meters of the water column ranged from 0.3 to 0.6 gC m -2 . The<br />
biomass composition of plankton assemblages among the stations<br />
was relatively uniform throughout the ice edge zone; however, the<br />
autotrophic flagellates and dinoflagellates showed significantly<br />
higher biomass at the ice edge or in open water relative to ice<br />
covered stations. The heterotrophic biomass (protozooplankton)<br />
exceeded the biomass of phytoplankton at most stations. Among the<br />
autotrophic forms, dinoflagellates made up 38% of the biomass,<br />
followed by other autotrophic flagellates (35%) and diatoms (27%).<br />
The phytoplankton biomass was dominated by nanoplankton ( 20 µm dominated the<br />
phytoplankton and standing stocks of Protozoa were lower, A. tonsa<br />
obtained 2.3% of its daily carbon intake from protozoan prey. In the<br />
subarctic North Pacific in June, where low phytoplankton standing<br />
stocks are dominated by cells < 5 µm, N. phlumchrus CV obtained<br />
11 - 18% of daily nutritional requirements from ciliate and<br />
dinoflagellate Protozoa > 5 µm and was capable of clearing 11-16%<br />
per day of the standing stock of Protozoa. In other protozoal taxa,<br />
which were present but not included directly in our experiments, are<br />
considered, N. plumchrus CV obtains potentially 28-59% of its daily<br />
metabolic requirements from ingestion of protozoan prey.<br />
Gorka, H. 1991. Les radiolaires du Turonien inférieur du<br />
sondage de Leba IG 1 (Pologne). Cah. Micropal., 6/1, 39-45.<br />
Lower Turonian Radiolarians (Polycystina) from the bore Leba IG<br />
I (Poland, baltic region) are abundant and well preserved. Nine<br />
species amongst spumellarians and six amongst nassellarians are<br />
described.<br />
Goto, H. & Ishiga, H. 1991. Study of late Ordovician<br />
<strong>radiolaria</strong>ns from the Lachlan Fold Belt, Southeastern<br />
Australia. Geol. Rep. Shimane Univ., 10, 57-62. (in<br />
Japanese)<br />
Gowing, M.M. & Garrison, D.L. 1991. Austral winter<br />
distributions of large tintinnid and large sarcodinid<br />
protozooplankton in the ice-edge zone of the Weddell/Sottia<br />
seas. J. Marine Syst., 2, 131-141.<br />
Seasonal distribution and abundance data for large sarcodinid<br />
protozooplankton (Radiolaria, Foraminifera, Acantharia and the<br />
heliozoan Sticholonche spp.) and larger tintinnid ciliates (e.g.,<br />
Laackmaniella spp.) are necessary for evaluating their roles in food<br />
webs and particle fluxes. As part of the Antarctic Marine Ecosystem<br />
Research in the Ice Edge Zone (AMERIEZ) project, we sampled these<br />
large ( ≥ 50 µm) protozooplankton in the winter ice edge zone of the<br />
Scotia/Weddell Seas. Organisms alive at the time of capture were<br />
counted in large volume (60 l) water samples from 5 paired depths<br />
- 63 -<br />
in the upper 2lO m from 17 stations. Relationships between<br />
abundances and environmental factors in ice-covered, ice edge, and<br />
open waters were assessed with correlation, cluster, and<br />
multidimensional scaling analyses.<br />
Mean abundances of large tintinnids were less than 3150 per<br />
m 3 , and mean abundances of the individual sarcodine groups were<br />
generally less than 1000 per m 3 . The most pronounced<br />
distributional patterns were related to depth. In general, large<br />
tintinnids were more abundant in the colder waters from 0-85 m, a<br />
zone encompassed by the mixed layer and the euphotic zone.<br />
Acantharians were more abundant in this upper zone only in icecovered<br />
waters. Radiolaria (predominantly phaeodarians), and the<br />
heliozoan Slicholonche spp. were more abundant from 115 to 210 m,<br />
a zone of warmer, more saline water. Foraminiferan distributions<br />
showed little pattern with depth. Results of the cluster analyses also<br />
suggested that depth was the most significant effect determining<br />
similarity among assemblages of large protozooplankton at the 17<br />
stations. The few correlations between abundances of the groups<br />
and chlorophyll a probably reflect relationships more complex than<br />
grazing.<br />
Abundances of large tintinnids were higher in surface waters<br />
under the ice than at the ice edge or in open water. This could result<br />
from their feeding on algal cells released from the base of the ice or<br />
it may be a result of higher populations in the outflow of Weddell Sea<br />
water. There were no consistent abundance patterns among large<br />
sarcodines that could be related to ice cover. It is suggested that<br />
the combination of low winter productivity, a dynamic environment,<br />
and slower growth rates of these large protozoans may prevent them<br />
from responding to local enhanced production with increased<br />
abundances in the winter ice edge zone. Furthermore, although there<br />
is enhanced productivity at the ice edge. this signal may not reach<br />
the protozooplankton groups most abundant in the water layer below<br />
the euphotic zone.<br />
Guex, J. 1991. Biochronological Correlations. , Springer-<br />
Verlag Berlin/Heidelberg/New York. , 250 p.<br />
The object of this book is to explain how to create a synthesis<br />
of complex biostratigraphic data, and how to extract from such a<br />
synthesis a relative time scale based exclusively on the fossil<br />
content of sedimentary rocks. Such a time scale can be used to<br />
attribute relative ages to isolated fossil-bearing samples.<br />
From a practical point of view, the method described in this<br />
book will particularly interest paleontologists and geologists who<br />
must construct zonations and establish correlations on the basis of<br />
biostratigraphic data that are both plentiful and apparently<br />
contradictory.<br />
It is well known that the difficulties involved in constructing<br />
biochronologic scales are largely due to the discontinuous nature of<br />
the fossil record. We know that the relationships between the first<br />
appearances (or disappearances) of different fossil species are<br />
rarely constant in stratigraphic sections that are distant from each<br />
other. It if often extremely difficult to discover datums or sets of<br />
species that are useful in making significant biochronologic<br />
correlations on a large scale.<br />
The theoretical model explained here (known as the Unitary<br />
Association Method) provides clear solutions to most of these<br />
problems. That method is purely deterministic, as opposed to<br />
statistical and probabilistic analytical techniques producing<br />
"average" ranges. We demonstrate in Chapter 15 why most of these<br />
techniques produce results which are usually not compatible with the<br />
original biostratigraphic observations (i.e., the taxonomic contents<br />
of the studied samples are not reproduced in the outputs).<br />
The syntheses used here are in the form of a referential (i.e., a<br />
system of chronologic reference); the chronologically significant<br />
subdivisions of these referentials correspond roughly to the<br />
Concurrent Range Zones and to the Oppel Zones of classical<br />
stratigraphy. These zones are seen here as discrete (i.e.,<br />
noncontiguous) units, isolated from each other by separation<br />
intervals.<br />
The operations required to construct such zonations are<br />
elementary but not always simple. We will begin by analyzing the<br />
fundamental properties of biochronologic referentials. This will<br />
enable us to assess the validity of stratigraphic correlations based<br />
on complex paleontological data. It will also help the reader master<br />
the mathematics and algorithms that are indispensable for making<br />
sense of the contradictory stratigraphic relationships so often<br />
observed among species in different locations. The ideas presented<br />
here were developed in a series of preliminary notes published<br />
between 1977 and 1984. To avoid excessive self-citations, we will<br />
mention in the text principally the ideas that are due to other<br />
authors.<br />
Two different computer programs making it possible to analyze<br />
certain complex biostratigraphic data are used a number of time in<br />
the present book. The oldest ones were written by Davaud and
Bibliography - 1991 Radiolaria 14<br />
published in collaboration with the author (Guex and Davaud 1982,<br />
1984, 1986). The last version of this program will be referred to as<br />
"DV-86". The most recent program, named "BioGraph", was<br />
developed on an IBM microcomputer by Savary (Savary and Guex<br />
1991). This very efficient program is described in Chapter 6. It is<br />
used to solve most of the difficult problems presented in this book.<br />
Gutschick, R.C. & Sandberg, C.A. 1991a. Upper<br />
Devonian biostratigraphy of Michigan Basin. In: Early<br />
sedimentary evolution of the Michigan Basin. (Catacosinos,<br />
P.A. & Daniels, P.A.J., Eds.), vol. 256. Geological Society<br />
of America, special Papers, pp. 155-179.<br />
The Late Devonian Michigan Basin was floored by the Middle and<br />
Upper Devonian Squaw Bay Limestone, which was deposited during<br />
the downwarping that produced the basin within a former Middle<br />
Devonian carbonate platform. The Squaw Bay comprises three beds,<br />
each having a different conodont fauna. The two upper beds,<br />
deposited during the transitans Zone, have different conodont<br />
biofacies that reflect this deepening. The basin was largely filled by<br />
the deep-water, anaerobic to dysaerobic, organic-rich, black Antrim<br />
Shale, which has a facies relationship with the prodeltaic, greenish<br />
gray Ellsworth Shale that prograded into the basin from the west. The<br />
Upper Devonian (Frasnian to Famennian) Antrim Shale is divided into<br />
four members, from base to top: the Norwood, Paxton, Lachine, and<br />
upper members. These members are more or less precisely dated by<br />
conodonts. The Norwood was deposited during the transitans Zone to<br />
Ancyrognathus triangularis Zone, and the Paxton was deposited from<br />
that zone probably through the linguiformis Zone at the end of the<br />
Frasnian. The overlying Lachine was deposited during the early<br />
Famennian and has yielded faunas of the Upper crepida and Lower<br />
rhomboidea Zones. Only the lower part of the upper member is<br />
exposed, and near Norwood, Michigan, it yielded conodonts of the<br />
Lower marginifera Zone. The widespread Famennian floating plant<br />
Protosalvinia (Foerstia) has not yet been found in outcrops of the<br />
Antrim, and should not be expected to occur except in the upper<br />
member or highest part of the Lachine Member. Its range in terms of<br />
conodont zones is from the Upper trachytera Zone through the Lower<br />
expansa Zone and possibly into the Middle expansa Zone. One known<br />
subsurface occurrence might be datable as rhomboidea or Lower<br />
marginifera Zone, depending on gamma ray correlations to outcrops.<br />
Black shale deposition ended when the Late Devonian mud delta of<br />
the Bedford Shale prograded across the Michigan Basin from the east<br />
and then retreated as the regressive Berea Sandstone was being<br />
deposited during the major eustatic sea-level fall that ended the<br />
Devonian. The Bedford was deposited during the Upper expansa to<br />
Lower praesulcata Zones, and the Berea was deposited during the<br />
Middle to Upper praesulcata Zones. Both formations contain the<br />
spore Retispora lepidophyta, which is a global indicator of latest<br />
Devonian age.<br />
Gutschick, R.C. & Sandberg, C.A. 1991b. Late<br />
Devonian history of Michigan Basin. In: Early sedimentary<br />
evolution of the Michigan Basin. (Catacosinos, P.A. &<br />
Daniels, P.A.J., Eds.), vol. 256. Geological Society of<br />
America, special Papers, pp. 181-202.<br />
The Upper Devonian sequence in the Michigan Basin is a<br />
westward extension of coeval cyclical facies of the Catskill deltaic<br />
complex in the Appalachian basin. Both basins and the intervening<br />
Findlay arch express the tectonic and sedimentational effects of<br />
foreland compression and isostatic compensation produced by the<br />
Acadian orogeny. The Late Devonian Michigan Basin formed as one of<br />
several local deeps within the long Eastern Interior seaway that<br />
separated the North American craton, backboned by the<br />
Transcontinental arch, on the west from the Old Red continent,<br />
Avalon terrane (micro-plate), and possibly northwest Africa on the<br />
east. Basin development began in the late Middle Devonian (late<br />
Givetian varcus Zone) with subsidence of a shallow-water carbonate<br />
platform formed by rocks of the Traverse Group. Subsidence was<br />
contemporaneous with Taghanic onlap of the North American craton.<br />
During subsidence, a thin transitional sequence of increasingly<br />
deeper water limestones separated by hardgrounds was deposited in<br />
the incipient Michigan Basin during the latest Givetian to earliest<br />
Frasnian disparilis to falsiovalis Zones. Deposition of this sequence<br />
culminated during the early Frasnian transitans Zone with a<br />
calcareous mudstone bed at the top of the Squaw Bay Limestone.<br />
Subsidence was followed by a 12-m.y.-long Late Devonian episode of<br />
slow, hemipelagic, basinal sedimentation of organic black muds that<br />
formed the Antrim Shale, interrupted basinwide only by deposition of<br />
its prodeltaic Paxton Member. Westward, the basinal Antrim black<br />
muds intertongued with greenish gray, deltaic and prodeltaic muds of<br />
an eastward-prograding delta platform formed by the Ellsworth<br />
Shale. Basinal black shale deposition ceased in latest Devonian (late<br />
Famennian Lower praesulcata Zone) time, when the Bedford deltaic<br />
complex prograded westward, completely filling the Antrim Basin and<br />
even covering part of the older Ellsworth deltaic complex on the<br />
west. As sea level was lowered eustatically near the end of the<br />
Devonian, the regressive Berea Sandstone terminated deltaic<br />
deposition. After an Early Mississippian erosional episode,<br />
- 64 -<br />
widespread deposition of the unconformably overlying Lower<br />
Mississippian Sunbury Shale began during the next transgression,<br />
associated with a major eustatic rise in the Lower crenulata Zone.<br />
Haslett, S.K. & Robinson, P.D. 1991.<br />
Micropaleontology notebook: detection of Radiolaria in the<br />
field. J. Micropaleont., 10/1, 22.<br />
Radiolaria can be preserved in all types of marine sedimentary<br />
rocks, the method for their extraction being dependent on the<br />
mineralogy of the <strong>radiolaria</strong>n test and the nature of the rock-type in<br />
which they occur. In the past <strong>radiolaria</strong> could only be viewed in thin<br />
section (Hinde, 1890; Hinde & Fox, 1895), with no method of<br />
detecting the presence of <strong>radiolaria</strong> prior to sectioning. Modern<br />
extraction techniques are normally laboratory based and use<br />
hazardous chemicals, therefore it is advantageous to establish the<br />
<strong>radiolaria</strong>n content of the sample before collection and<br />
transportation back to the laboratory. This can be achieved in a<br />
number of ways: non-lithified sediments, siliceous rock-types,<br />
limestone, phosphate nodules and argillites<br />
Hernández-Molina, F.J., Sandoval, J., Aguado,<br />
R., O'Dogherty, L., Comas, M.C. & Linares, A.<br />
1991. Olistoliths from the Middle Jurassic in Cretaceous<br />
materials of the Fardes formation. Biostratigraphy (Subbetic<br />
Zone, Betic Cordillera). Rev. Soc. geol. España, 4/1-2, 79-<br />
104.<br />
The Middle Jurassic olistoliths studied are found within<br />
Cretaceous materials of the south-eastern part of the Montes<br />
Orientales region (province of Granada, Betic Cordillera), specifically<br />
in the Rio Fardes sector. The cretaceous materials are here<br />
characterized by pelagic and hemipelagic facies with abundant<br />
turbidite and olistostrome insertions in a deep basin marine<br />
environment (Middle Subbetic), bounded to the SE by a pelagic ridge<br />
(Internal Subbetic). The transition between the two domains was an<br />
area with active paleoslopes which facilitated both the exposure and<br />
denudation of Jurassic and Cretaceous materials and the<br />
development of a clear synsedimentary tectonics (slumps and<br />
olistostromes). Paleocurrents show that the source area of<br />
materials forming the thickest beds was located towards the S-SW,<br />
though for the thinner beds they are more widely dispersed.<br />
The sections under study have been dated by means of<br />
calcareous nannoplankton, planktonic foraminifera and <strong>radiolaria</strong>.<br />
The calcareous nannofossil assemblages enable us to distinguish<br />
Sissingh's zones CC-9, CC-10 and CC-13 for the Lower<br />
Cenomanian-Coniacian, which in turn determines the position of the<br />
Jurassic olistoliths within the sections. The precise age of the<br />
materials where the large-sized olistoliths are embedded is<br />
Coniacian (Marthasterites furcatus zone of calcareous<br />
nannoplankton).<br />
Olistoliths from the Middle Jurassic are often sufficiently<br />
exposed and stratified to allow sampling level by level and the<br />
establishing of a detailed biostratigraphy. After a study of the<br />
ammonite fauna collected in two olistoliths we were able to<br />
distinguish the Murchisonae and Concavum zones in the Aalenian,<br />
and the Discites, Laeviuscula, Sauzei and Humphriesianum zones in<br />
the Bajocian.<br />
In those areas with S-SW paleocurrents Aalenian materials are<br />
not found, but the Bajocian materials of some nearby sectors<br />
belonging to the Internal Subbetic have a similar lithology and faunal<br />
content.<br />
Hollis, C.J. & Hanson, J.A. 1991. Well-preserved late<br />
Paleocene Radiolaria from Tangihua Complex, Camp Bay,<br />
eastern Northland. Tane, 33, 65-76.<br />
A sparse but very well-preserved <strong>radiolaria</strong>n fauna has been<br />
obtained from interpillow limestone in the allochthonous Tangihua<br />
Complex at Camp Bay, northwest of Whangaroa Harbour. A Late<br />
Paleocene age (58-62 Ma) is probable; primarily because of the<br />
presence of Buryella cf. tetradica Foreman, a variant of B. tetradica<br />
known only from the Paleocene, and the absence of Early Paleocene<br />
or latest Paleocene-Eocene index species. This is the first<br />
unequivocal record of Tertiary fossils from Tangihua sediments. The<br />
assemblage suggests upper-mid bathyal, warm-temperate conditions<br />
of deposition.<br />
The good state of preservation and the presence of established<br />
index species show that <strong>radiolaria</strong>ns have potential for improving<br />
age control and clarifying the depositional conditions of sediments<br />
associated with Tangihua igneous massifs.<br />
Hull, D.M. 1991. Upper Jurassic <strong>radiolaria</strong>n<br />
biostratigraphy of the lower member of the Taman<br />
Formation, east-central Mexico and of volcanopelagic strata
Radiolaria 14 Bibliography - 1991<br />
overlying the Coast Range ophilite, Stanley Mountain,<br />
Southern California Coast Range. Ph.D. Thesis. Programs in<br />
Geoscience, University of Texas at Dallas, 696 p.<br />
(unpublished)<br />
Ishida, K. & Hashimoto, H. 1991. The problem on<br />
<strong>radiolaria</strong>n shells reworking into the Lower Cretaceous<br />
molluscan facies in Chichibu Terrane, eastern Shikoku. J.<br />
sedimentol. Soc. Japan, 34, 15-20. (in Japanese)<br />
Some Middle-Late Jurassic <strong>radiolaria</strong>n shells were detected<br />
associated with Early Cretaceous autochthonous <strong>radiolaria</strong>n and<br />
anmmonite assemblages from the Lower Cretaceous formations of<br />
molluscan facies in eastern Shikoku.<br />
The modes of occurrence on these Middle-Late Jurassic<br />
<strong>radiolaria</strong>n shells were summarized as follows: 1) Specific diversity<br />
of associate Middle-Late Jurassic <strong>radiolaria</strong>ns are restricted within<br />
several species of Tricolocapa and Stichocapsa genera. 2) Most of<br />
these Jurassic <strong>radiolaria</strong>ns are subspherical with closed distal end in<br />
shape. 3) Their sizes are limited to 100-150 µm in length and 80-<br />
100 µm in diameter. 4) Lithologically, they are contained in<br />
laminated sandy mudstones and sandy siltstones. 5) Among these<br />
older <strong>radiolaria</strong>ns, Tricolocapsa plicarum, T. conexa, T. fusiformis ?,<br />
Stichocapsa convexa and S. naradaniensis are the index species of<br />
Middle to early Late Jurassic age. But the other species whose final<br />
appearances are known within Earliest Cretaceous such as<br />
Cinguloturris carpatica, Pseudodictyomitra primitiva and<br />
Eucyffidiellum pyramis have possibility that their ranges reach into<br />
Barremian age. 6) All these Jurassic elements are yielded from the<br />
first transgressive sediments successively just above the Lower<br />
Cretaceous nonmarine formations in the Northern and the Middle<br />
Chichibu Terranes. 7) These ammonites and <strong>radiolaria</strong>ns bearing<br />
Lower Cretaceous formations are the continental shelf or upper<br />
submarine terrace sediments, because they construct cyclothem<br />
together with the coal-bearing and blackish sediments which<br />
unconformably overlie both the melange type Jurassic formations in<br />
the Northern Chichibu Terrane and the molluscan facies Middle-Late<br />
Jurassic formations in the Middle Chichibu Terrane.<br />
The above-mentioned evidences showed that these Jurassic<br />
<strong>radiolaria</strong>n shells are the reworked fossils in the same manner as<br />
other detrital clastics in the Cretaceous sediments, probably derived<br />
from the Pre-Cretaceous basement similar to the Northern and the<br />
Middle Chichibu Terranes. Therefore, it is necessary to consider the<br />
problem of reworking and mixing by older materials when we deal<br />
with the microfossil biostratigraphy at nearshore sediments on such<br />
continental shelf and/or upper submarine terrace.<br />
Ishida, K. & Hashimoto, H. 1991. Radiolarian<br />
assemblages from the Lower Cretaceous formation of the<br />
Chichibu Terrane in eastern Shikoku and their ammonite<br />
ages. J. Sci., Univ. Tokushima, 25, 23-67. (in Japanese)<br />
Lower Cretaceous <strong>radiolaria</strong>n biostratigraphy is studied in the<br />
molluscan facies strata of the Chichibu Terrane in eastern Shikoku.<br />
Chronological order of each assemblage obtained from 14 localities<br />
is estimated statistically on the basis of known specific ranges.<br />
Three <strong>radiolaria</strong>n assemblage zones are newly proposed and are tied<br />
to chronostratigraphy by means of coexisting ammonites. They are<br />
Archaeodictyomitra pseudoscalaris Assemblage Zone of Barremian<br />
age, Stichomitra communis Assemblage Zone of middle Aptian age,<br />
and Pseudodictyomitra pentacolaensis Assemblage Zone of Late<br />
Albian age. Among the 65 species, identified, listed and figured, the<br />
first appearances of 10 species and the final appearances of 15<br />
species are newly ascertained. The proposed zones are correlated<br />
with those of proposed by other authors in pelagic and non shallowmarine<br />
facies.<br />
Ishiga, H. 1991. "Dimorphic pairs" of Albaillellaria (late<br />
Paleozoic Radiolaria), Japan. Mem. Fac. Sci., Shimane<br />
Univ., 25, 119-129.<br />
Ishiga, H. 1991. Description of a new Follicullus species<br />
from southwest Japan. Mem. Fac. Sci., Shimane Univ., 25,<br />
107-118.<br />
Johnson, L.E., P., F., Taylor, B., Silk, M.,<br />
Jones, D.L., Sliter, W.V., Itaya, T. & Ishii, T.<br />
1991. New evidence for crustal accretion in the outer Mariana<br />
fore arc: Cretaceous <strong>radiolaria</strong>n cherts and mid-ocean ridge<br />
basalt-like lavas. Geology, 19, 811-814.<br />
New age determinations on radio1arian cherts, foraminifers,<br />
and volcanic rocks document the presence of allochthonous<br />
fragments of Cretaceous oceanic plate, suggesting accreted<br />
terrane, in the outer Mariana fore arc, more than 50 km from the<br />
- 65 -<br />
trench. Three dredges, from a 3 km 2 area along a steep scarp,<br />
recovered a diverse assemblage of rocks representing an ophiolite<br />
suite (chert, mafic and intermediate lavas and intrusive rocks).<br />
Trace element patterns of the lavas suggest at least three tectonic<br />
associations (island arc, ocean island, and oceanic plate). The cherts<br />
contain two deep-water assemblages of <strong>radiolaria</strong> of middle to late<br />
Valanginian (131-138 Ma) and Albian (97-112 Ma) age.<br />
Foraminifers recovered with the chert are Aptian to Albian in age.<br />
The lavas record a wide range of K-Ar ages, 85 Ma for a metabasalt<br />
with trace-element signatures of mid-ocean ridge basalt, 71 Ma for<br />
a highly metamorphosed alkalic basalt, and 39 Ma for a fresh glassy<br />
boninite. These ages imply multiple volcanic events and at least two<br />
tectonic settings for magma genesis. The cherts and metabasalts<br />
are too old to have formed in situ or to be part of trapped West<br />
Philippine Basin crust. The mix of old oceanic plate with younger arc<br />
rocks requires complex tectonic relations. We suggest that one or<br />
more fragments of Cretaceous oceanic plate (chert, mid-ocean ridge<br />
basalt, and alkalic lavas) were accreted to the Mariana fore arc and<br />
have been extensively faulted and probably intruded by arc lava<br />
(island-arc tholeiite and boninite).<br />
Jud, R. 1991. Bichronology and systematics of Early<br />
Cretaceous Radiolarian of the Western Tethys. Ph.D. Thesis.<br />
University of Lausanne, 147 p. (unpublished)<br />
About 500 samples of Uppermost Jurassic to Lowermost<br />
Aptian cherty limestones, most of them in the Maiolica facies, were<br />
studied for their contents in <strong>radiolaria</strong>ns in order to make a<br />
comprehensive inventory of <strong>radiolaria</strong>n assemblages and to<br />
establish a <strong>radiolaria</strong>n biochronology calibrated and correlated to the<br />
magnetostratigraphy established in the same sections and to<br />
biozonations of other fossil groups. The samples were collected from<br />
26 land sections in Switzerland, Italy and Oman. Of several hundred<br />
morphotypes recorded in 245 well preserved samples from only 13<br />
sections of the 26 examined, 175 <strong>radiolaria</strong>n taxa were selected,<br />
and species occurrences were calculated with the computer program<br />
"BIOGRAPH" (Savary & Guex, 1990). This resulted in 35 successive<br />
Unitary Associations (U.A.) that could be grouped into 11 biozones<br />
whose terminology follows and continues that of Baumgartner<br />
(1984b). A protoreferential or "range chart" based on U.A. was<br />
finally synthetised for all species selected between the interval of<br />
the Middle Tithonian and the Lowermost Aptian.<br />
The 11 <strong>radiolaria</strong>n zones (C1-G2) were correlated to magnetic<br />
polarity chrons, calpionellid zones and nannofossil events<br />
established by previous workers on the investigated sections.<br />
Diachrony in correlating the <strong>radiolaria</strong>n zones is probably caused by<br />
several reasons among which lithostratigraphy, species definition<br />
and abundance, calibration with magnetic chrons and definition of<br />
these chrons are among the most important.<br />
Although the studied sections belong to several distinct<br />
paleogeographic areas with basinal and seamount facies: Prealpine<br />
Nappes (Northern Tethys), Southern Alps and Umbria Marche<br />
Apennines (Apulian Plate, Southern Tethys) and Hawasina Complex<br />
(distal Arabian Margin), the <strong>radiolaria</strong>n Unitary Associations have<br />
proved to be a useful tool for correlation.<br />
Precise correlation of the new <strong>radiolaria</strong>n zonation, based on<br />
the co-existence of several species within one zone, to most of the<br />
previous <strong>radiolaria</strong>n zonations is impossible or very difficult,<br />
because most of them were defined by first or last appearances of<br />
one or two "marker" species, which may greatly differ from section<br />
to section.<br />
The time span covered by the new <strong>radiolaria</strong>n biozones is<br />
variable. Zone E2 has a duration of less than I million years whereas<br />
zone E1b spans about 4 million years. Zone E2 is located in the<br />
Middle Valanginian at the base of the magnetic polarity zone M11<br />
and corresponds, in the Southern Alps, to a time of elevated ∂ 13 C<br />
values (Weissert & Lini, 1991). During this characteristic period,<br />
explained by the authors as an episode of greenhouse climate, pelitic<br />
intervals, elevated bioturbation and cyclic sedimentation occurred.<br />
The same interval (Zones E2 and F1 corresponding to the Middle and<br />
the Upper Valanginian) is also characterized by the abundance of<br />
some taxa in the samples of the Fiume Bosso section.<br />
All the 175 taxa investigated, of which 1 new subspecies, 61<br />
new species and 2 new genera, are described and illustrated in the<br />
systematic part of the thesis.<br />
Kamata, Y., Sashida, K. & Igo, H. 1991. Geology of<br />
the Cretaceous Masutomi Group exposed in the southwestern<br />
part of the Kanto Mountains, central Japan. J. geol. Soc.<br />
Japan, 97/2, 157-169. (in Japanese)<br />
The stratigraphy and ages of the Masutomi Group are discussed<br />
based on recent fossil findings The Masutomi Group is subdivided<br />
into the following three formations from north to south, the Albian to<br />
Maastrichtian Takatoyasan Formation; the late Campanian to early<br />
Maastrichtian Mikado Formation; and the late Albian to
Bibliography - 1991 Radiolaria 14<br />
Maastrichtian Madarayama Formation. Based on the stratigraphical<br />
features and <strong>radiolaria</strong>n dating, the Takatoyasan Formation is<br />
presumed to be a product of the convergent complex of an oceanic<br />
plate in trench environment The structure and sedimentary facies of<br />
the Mikado and Madarayama Formations are comparable to those of<br />
the Cretaceous Shimanto Belt in Shikoku and Kii.<br />
Kiesling, W. & Zeiss, A. 1991/92. New<br />
palaeontolgical data from the Hochstegen Marble (Tauern<br />
window, eastern Alps). Geol. Pälont. Mitt. Innsbruck, 18,<br />
187-202.<br />
Two new species and one new genus of Radiolaria are described<br />
from the greenschist-metamorphic Hochstegen Marble of the Tauern<br />
Window. Despite of strong shearing deformation the microstructure<br />
is sufficiently preserved for species determination, due to early<br />
diagenetic pyritization of the siliceous skeletons. The new<br />
<strong>radiolaria</strong>ns belong to a Kimmeridgian to Lower Tithonian<br />
assemblage. They are part of a highly diverse fauna of <strong>radiolaria</strong>ns<br />
and sponge spicules recovered from the HCI-insoluble residue of the<br />
Hochstegen Marble.<br />
The famous 'ammonite from the street wall' could firstly be<br />
determined on a species level as Orthosphinctes (Lithacosphinctes)<br />
siemiradzkii n.nom. [pro 'O. (L.) evolutus QUENSTEDT]. The ammonite<br />
is proof of Uppermost Oxfordian age for the dolomite quarry near<br />
Mayrhofen. The taxonomical and nomenclatorical problems of the O<br />
.(L.) siemiradzkii as well as that of the related species O. (O.)<br />
polygyratus and O. (O.) tiziani are explained in detail.<br />
Kito, N. & Chitoku, T. 1991. Geologic age of the<br />
mosasaurian fossil from Hobetsu-cho, Hokkaido, Japan. Sci.<br />
Rep. Hobetsu Mus., Hokkaido, 7, 9-14. (in Japanese)<br />
Kojima, S., Wakita, K., Okamura, Y., Natal'in,<br />
B.A., Zyabrev, S.V., Qing, L.Z. & Ji, A.S. 1991.<br />
Mesozoic <strong>radiolaria</strong>ns from the Khabarovsk Complex,<br />
eastern USSR; their significance in relation to the Mino<br />
Terrane, central Japan. J. geol. Soc. Japan, 97/7, 549-551.<br />
In the course of the geotectonic studies on "geosynclines" in<br />
Northeast Asia, Japanese geologists (e.g, Kobayashi, 1984; Noda,<br />
1956) have focused their interests on the complicated sedimentary<br />
formations in the Sikhote-Alin region in relation to the Japanese<br />
"Paleozoic" stratigraphy. Especially, Noda (1956) introduced the<br />
occurrence of Radiolaria bearing siliceous formations near<br />
Khabarovsk, although he regarded the rocks as the Permian. After<br />
that, Russian paleontologists and biostratigraphers have reported<br />
Mesozoic <strong>radiolaria</strong>ns from the Sikhote-Alin Range, including the<br />
Khabarovsk area (e.g, Zhamoida, 1972; Tikhomirova, 1986); most<br />
of their works, however, were based on observations under the<br />
optical microscope.<br />
In this article, we describe the occurrence of Triassic and<br />
Jurassic <strong>radiolaria</strong>ns from the Khabarovsk complex, eastern USSR<br />
(stipple pattern in the inset map of Fig. 1), and discuss<br />
paleontological, stratigraphical and structural similarities between<br />
the Khabarovsk complex and the Mino terrane in central Japan.<br />
Kozur, H. 1991. The evolution of the Meliata-Hallstatt<br />
ocean and its significance for the early evolution of the<br />
Eastern Alps and Western Carpathians. Palaeogeogr.<br />
Palaeoclimatol. Palaeoecol., 87/1-4, 109-135.<br />
The evolution of the Meliata-Hallstatt ocean and of its southern<br />
and northern margin in the Inner Western Carpathians are described.<br />
The main rifting began during the Pelsonian and the sea-floor<br />
spreading ended at the beginning of the Middle Carnian<br />
contemporaneously with the Raibl event. The subduction began in the<br />
latest Triassic and the final closing of the ocean, accompanied by<br />
uplift of the adjacent marginal areas, was dated as basal Oxfordian.<br />
Remnants of the oceanic-suboceanic sequence occur in two tectonic<br />
positions: (I) Obducted nappes that contain, mostly as tectonic<br />
melanges, the whole Middle Triassic to Middle Jurassic sequence,<br />
including large bodies of dismembered ophiolites of Ladinian to Early<br />
Carnian age. (2) Evaporite melanges at the base of nappes that are<br />
derived from the northern margin of the ocean. These evaporite<br />
melanges consist of Late Permian evaporitic matrix and blocks of a<br />
dismembered Ladinian to Lower Carnian ophiolitic sequence.<br />
In the Inner Western Carpathians both the northern and southern<br />
marginal sequences of the Meliata-Hallstatt ocean and the<br />
transitions into the carbonate platforms are present in different<br />
nappes. The southern marginal development is characterized by<br />
Middle Carnian distal clastic Raibl Beds and by Middle Jurassic<br />
rhyolithic volcanism, both missing in the northern marginal<br />
development. Because the subduction-related Middle Jurassic<br />
volcanism (contemporaneous with the turbidites in the southern<br />
- 66 -<br />
Meliaticum) is restricted to the marginal area south of the Meliata-<br />
Hallstatt ocean, southward-directed subduction is indicated. To the<br />
south, on the adjacent carbonate platform, a Jurassic basin with<br />
Aalenian to Bajocian ophiolites opened. This may be a back-arc basin.<br />
In the Eastern Alps only the northern marginal zone and the<br />
adjacent carbonate platform are preserved, but parts of the<br />
dismembered ophiolites in the Haselgebirge may be of Ladinian to<br />
Late Carnian age like in evaporitic melanges in the same tectonic<br />
position in the Inner Western Carpathians.<br />
The final closing of the Meliata-Hallstatt ocean is indicated by<br />
the abrupt end of the turbiditic sedimentation in the oceanic<br />
suboceanic domain and by uplift in the marginal areas, where Lower<br />
Oxfordian radiolarites are overlain by shallow-water Upper Oxfordian<br />
to Tithonian or Neocomian limestones (Silica Nappe, Hallstatt<br />
Nappes). With the evidence of the final closing of the Meliata-<br />
Hallstatt ocean near the Middle/Late Jurassic boundary, the<br />
Cimmerian orogenesis (in the genetic sense of Sengor, 1984, 1985)<br />
is now also proven in the Inner Western Carpathians and in the<br />
Eastern Alps.<br />
A continuation of the Meliata-Hallstatt ocean into the Pontide<br />
"Paleotethys" (=Cimmerian ocean sensu Kozur, 1990) through the<br />
Transylvanian oceanic domain and the Strandzha Unit is assumed. A<br />
connection with the Vardar ocean is impossible, because in the<br />
Vardar Zone no Triassic ophiolites or basic volcanics are present and<br />
the ophiolites have Jurassic age.<br />
Kozur, H. & Mostler, H. 1991. Erster<br />
paläontologischer nachweis von meliaticum und südrudabányaicum<br />
in den nördlichen kalkalpen (Östereich) und<br />
ihre beziehungen zu den abfolgen in den westkarpaten. Geol.<br />
Pälont. Mitt. Innsbruck, 18, 87-129.<br />
For the first time, a sedimentary sequence of the Meliaticum<br />
has been paleontologically dated by conodonts and <strong>radiolaria</strong>ns in<br />
the Northem Calcareous Alps . Middle Triassic red radiolarites,<br />
silicified pelagic red limestones ( ' chert ' ) and subordinately pelagic<br />
limestones occur as olistoliths in a Middle Jurassic sequence of<br />
partly graded shales and siltstones, some sandstones and numerous<br />
olistoliths. This sedimentary Meliaticum that has been found at the<br />
Florianikogel and in the Edenhof window, is part of a nappe named as<br />
Florianikogel Nappe. In the Edenhof multiple window, serpentinit is<br />
present subordinately. At the Florianikogel light-coloured, crystalline<br />
limestones of the pre-(oceanic) rift stage are present that can be<br />
also found in marginal suboceanic parts of the Meliaticum in the<br />
Westem Carpathians. Tectonically dismembered ophiolites of the<br />
Meliaticum are present in a narrow E-W to ENE-WSW striking zone<br />
running from Unter-Hoflein in the east across Pfennigbach, western<br />
Mariazell-Puchberg line to Grundlsee in the west. These ophiolites<br />
occur mostly in salinar melanges. They indicate seemingly the suture<br />
zone of the Meliata-Hallstatt ocean. This zone is narrow and no<br />
segments of this zone are displaced distinctly in N-S direction.<br />
Therefore a large-scale nappe transport of upper parts of the<br />
original suture of the Meliata-Hallstatt ocean from the area near to<br />
the Alpin-Dinaric Line is not probably. The tectonic consequences for<br />
the nappe structure of the Eastem Alps are discussed.<br />
Unmetamorphic South-Rudabanyaicum was found near the southem<br />
margin of the Northem Calcareous Alps . These units were originally<br />
situated south of the Meliata-Hallstatt ocean. The Geyerstein Nappe<br />
is introduced for this sequence. Additionally, low-grade metamorphic<br />
remnants of South-Rudabanyaicum are present in the Edenhof<br />
multiple window. The upper part of the Lower Anisian and the Lower<br />
Pelsonian are pelagic and in the Pelsonian reworked basic volcancis<br />
can be found beside numerous reworked limestones. These basic<br />
volcancis indicate a transitional position of this South-<br />
Rudabanyaicum to the Meliaticum.<br />
Kurimoto, C. & Kuwahara, K. 1991. Radiolarians from<br />
the Ojigahata area of Shiga Prefecture, southwestern part of<br />
the Mino Terrane. Bull. geol. Surv. Japan, 42/2, 63-73. (in<br />
Japanese)<br />
Strata of the Mino Terrane which are distributed in the study<br />
area are called the Ojigahata Formation. The Ojigahata Formation<br />
consists mainly of chert associated with mudstone and sandstone,<br />
and belongs to the sandstone-chert facies of the Mino Terrane.<br />
Chert and mudstone of the Ojigahata Formation were collected to<br />
extract microfossils. As a result, <strong>radiolaria</strong>ns available for agedetermination<br />
were obtained from 12 samples. Radiolarian<br />
assemblages from chert are correlated with those of Middle Triassic,<br />
Late Triassic and Early Jurassic ages. On the other hand, <strong>radiolaria</strong>n<br />
assemblages from mudstone are correlated with those of middle<br />
Middle Jurassic and late Middle to early Late Jurassic ages. Judging<br />
from the above-mentioned data, the Ojigahata Formation represents<br />
a coarsening-upward sequence which consists of Middle Triassic to<br />
Early Jurassic chert, Middle Jurassic mudstone and Middle to Late<br />
Jurassic interbedded sandstone and mudstone.
Radiolaria 14 Bibliography - 1991<br />
Kuwahara, K., Nakae, S. & Yao, A. 1991. Late<br />
Permian "Toishi-type" siliceous mudstone in the Mino-<br />
Tamba Belt. J. geol. Soc. Japan, 97/12, 1005-1008. (in<br />
Japanese)<br />
Lackschewitz, K.S., Grützmacher, U. & Henrich,<br />
R. 1991. Paleoceanography and Rotational Block Faultinf in<br />
the Jurassic Carbonate Series of the Chiemgau Alps (Bavaria).<br />
Facies, 24, 1-24.<br />
The Jurassic carbonate series of the Lechtal and Allgau Nappes<br />
in the central part of the Northern Calcareous Alps reflect formation<br />
of orogen-parallel structures with swells and basins. Regional facies<br />
patterns display the morphologies of the various depositional<br />
environments.<br />
During the Middle Jurassic, an elongated swell evolved parallel<br />
to the overall structural strike in the central part of Lechtal Nappe,<br />
while in the southern part a basin started to subside. This<br />
configuration reflects the initial stage of rotational block faulting on<br />
the southern continental margin of the Tethys. Similar structural and<br />
facies settings were also established in the northern part of the<br />
Lechtal Nappe and in the southern Allgau Nappe. Synsedimentary<br />
tectonics induced a variety of downslope sediment mass movements<br />
and increased facies differentiation on the slopes. In the upper<br />
section of the middle Jurassic sequences red nodular limestones<br />
with frequent intercalations of intraformational breccias and<br />
conglomerates indicate downslope sediment movements.<br />
During the Oxfordian, the Tethyan-wide deposition of<br />
radiolarites also covered the basin in the southern Lechtal Nappe.<br />
Contemporaneous deposition of pelagic <strong>radiolaria</strong>n bearing<br />
limestones dominated on the slope of the surrounding northern swell,<br />
while its peak was covered by a shallow water carbonate facies, e.g.<br />
a specific pseudopeloid and oolithic facies, which was also injected<br />
downslope into the pelagic facies.<br />
The Oxfordian to Tithonian section reveals a characteristic<br />
pelagic carbonate facies succession, e.g. with Protoglobigerina<br />
facies at the base, followed by a Saccocoma facies and a<br />
calpionellids facies on top. In the northern Lechtal Nappe and in the<br />
Allgau Nappe various similar radiolarite basins with intersected<br />
swells were discovered.<br />
Leynaert, A., Treguer, P., Queguiner, B. &<br />
Morvan, J. 1991. The distribution of biogenic silica and<br />
the composition of particulate organic matter in the Weddell-<br />
Scotia Sea during spring 1988. Marine Chem., 35, 435-447.<br />
During EPOS 2 (European Polarstern Study, leg 2, 26 November<br />
1988-5 January 1989 the distribution of biogenic silica (BSi) was<br />
determined from the surface to 600 m along two transects (49 o W<br />
and 47 o W) spanning the Scotia Sea; the Weddell-Scotia Confluence<br />
(WSC) and the marginal ice zone (MIZ) of the Weddell Sea.<br />
Parliculate organic carbon (POC), particulate organic nilrogen (PON)<br />
and chlorophyll a concentrations were determined in parallel in<br />
surface ( 10 m ) samples.<br />
In the 0-100 m layer, the distribution of particulate biogenic<br />
silica (BSi) showed little correlation with the meltwater field in late<br />
November. High BSi concentrations were measured at the end of<br />
November in the Weddell-Scotia Confluence ( maximum 4.8 µmol l -<br />
1<br />
), and early in January in the Antarctic Circumpolar Current (<br />
maximum at 8.2 µmol l -1 ) where the wind-mixed layer was only 35 m,<br />
creating favourable conditions for phytoplankton growth. However,<br />
maximum and mean biogenic silica values remained fairly low as<br />
compared with those reported for the Ross Sea. This relatively low<br />
silica content of the 0-100 m layer appears to be mainly due to<br />
intense grazing which resulted in rapid exportation of particulate<br />
material towards the deeper layers.<br />
The mean POC/PON molar ratio was 5.5, i.e. significantly lower<br />
than the usual Redfield ratio. BSi/POC molar ratios ranged from 0.01<br />
to 0.61, the highest values being found in the Scotia Sea, where<br />
siliceous phytoplankton was dominant. The high BSi/POC ratios<br />
confirm that diatoms in Antarctic Ocean are able to incorporate<br />
unusually high amounts of Si relative to carbon, as compared with<br />
other ecosystems.<br />
Li, Y.X. & Wang, Y.J. 1991. Upper Devonian<br />
(Frasnian) <strong>radiolaria</strong>n fauna from the Liukiang Formation,<br />
eastern and southeastern Guangxi. Acta micropalaeont.<br />
sinica, 8/4, 395-404. (in Chinese)<br />
The siliceous rocks of the Upper Devonian Liukiang Formation<br />
are widely distributed, in eastern and southeastern Guangxi.<br />
Abundant fossil <strong>radiolaria</strong>ns and tentaculitids are found in these<br />
rocks, with 4 genera and 14 species including 1 new genus and 2<br />
new species of the <strong>radiolaria</strong>ns described in this paper.<br />
- 67 -<br />
The tentaculitid faunas are dominated by the genera<br />
Homoctenus, Costulatostyliolina and Styliolina, with Styliolina<br />
philippovae and S. domanicensis regarded as important members of<br />
the Upper Devonian Frasnian Stage in the Russian Platform and<br />
Germany. The <strong>radiolaria</strong>n faunas are characterized by a great<br />
number of species and individuals of the genus Entactinosphaera<br />
such as Entactinosphaera assidera, E. egindyensis, E. aitpaiensis, E.<br />
vetusta, together with Entactinia dissora and Palaeoscenidium<br />
cladophorum, which were already discovered in the Frasnian<br />
Egindinsk Formation of the South Urals (Nazarov, 1975) and<br />
Australia (Hinde, 1899; Nazarov et al., 1982; Nazarov & Ormiston,<br />
1983), indicating that the age of the Liukiang Formation is Late<br />
Devonian (Frasnian).<br />
Ling, H.Y. 1991a. Tripylean <strong>radiolaria</strong>ns from the<br />
Subantarctic Atlantic. In: Proceedings of the Ocean Drilling<br />
Program, Scientific Results. (Ciesielski, P.F., Kristoffersen,<br />
Y. et al., Eds.), vol. 114. College Station, TX (Ocean<br />
Drilling Program), pp. 311-315.<br />
The occurrence of tripylean <strong>radiolaria</strong>ns is reported for the first<br />
time from subsurface sediments of the subantarctic Atlantic Ocean.<br />
Although their occurrence is rare as well as sporadic, seven species<br />
belonging to four genera are recognized from Upper Cenozoic<br />
sediments drilled at Sites 699, 700, and 701 of ODP Leg 114 in<br />
1987.<br />
Ling, H.Y. 1991b. Cretaceous (Maestrichtian)<br />
<strong>radiolaria</strong>ns: Leg 114. In: Proceedings of the Ocean Drilling<br />
Program, Scientific Results. (Ciesielski, P.F., Kristoffersen,<br />
Y. et al., Eds.), vol. 114. College Station, TX (Ocean<br />
Drilling Program), pp. 317-324.<br />
Cretaceous <strong>radiolaria</strong>ns were recovered from subantarctic<br />
Atlantic calcareous submarine deposits from two of the seven sites<br />
drilled during ODP Leg 114 in 1987. Fairly well-preserved<br />
<strong>radiolaria</strong>n assemblages were found in Hole 698A samples from the<br />
Northeast Georgia Rise, whereas assemblages with fair to good<br />
preservation were observed from Hole 700B in the East Georgia<br />
Basin. The assemblage compositions from both sites are rather low<br />
in diversity and are characterized by the dominance of<br />
Protoamphipyndax, Dictyomitra, and Stichomitra species, but lack<br />
zonal markers recognized from the midlatitude to low-latitude<br />
region. Assignment of a Maestrichtian age is based on co-occurring<br />
calcareous microfossils. This report constitutes the second such<br />
occurrence from the Atlantic sector of the Antarctic Ocean<br />
subsequent to the analysis of ODP Leg 113 materials from the<br />
Weddell Sea.<br />
Ling, H.Y., Hall, R. & Nichols, G.J. 1991. Early<br />
Eocene Radiolaria from Waigeo Island, Eastern Indonesia. J.<br />
Southeast Asian Earth Sc., 6/3-4, 299-305.<br />
The recovery of well-preserved Early Eocene <strong>radiolaria</strong>n<br />
assemblages confirms the presence of Paleogene marine sediments<br />
in Waigeo Island. Eastern Indonesia.<br />
Marchant, H.J. & Wright, S.W. 1991. Species<br />
composition distribution and abundance of Antarctic marine<br />
protists. Austral. antarct. Res. Programm, 140-143.<br />
Marcucci, M et al. 1991. Interrad VI, Sixth Meeting of<br />
the International Association of Radiolarian Paleontologists;<br />
abstracts book. , Florence, Italy. 126 p.<br />
Marcucci, M. & Passerini, P. 1991. Radiolarianbearing<br />
siliceous sediments in the Mesozoic of the northern<br />
and central Apennines. Ofioliti, 16/2, 121-126.<br />
Radiolarian-bearing siliceous deposits are a common<br />
occurrence in the Mesozoic successions of the Northern and Central<br />
Apennines. These deposits belong to the following stratigraphic<br />
units: 1) Monte Alpe Cherts. Early Callovian to Late Tithonian or<br />
Early Berriasian. 2) Tuscan Cherts. Latest Bajocian(?)-Early<br />
Bathonian to Late Tithonian or Early Berriasian. 3) "Calcari<br />
Diasprigni". Late Bajocian(?)-Bathonian to Tithonian. 4) Fucoid Marls<br />
(Umbrian succession). Aptian-Albian. 5) Carbonate-shaly-siliceous<br />
complex of Monti della Meta. Albian 6) Bonarelli Horizon (Umbrian<br />
succession) Late Cenomanian to (?)Early Turonian. 7) "Scisti<br />
Policromi" (Tuscan succession). Cenomanian-Turonian interval. 8)<br />
Fosso Cupo Formation Turonian to Santonian.<br />
Marcucci-Passerini, M., Bettini, P., Dainelli, J.<br />
& Sirugo, A. 1991. The "Bonarelli Horizon" in the central<br />
Apennines (Italy): <strong>radiolaria</strong>n biostratigraphy. Cretaceous<br />
Res., 12/3, 321-331.
Bibliography - 1991 Radiolaria 14<br />
The "Bonarelli Horizon", of Cenomanian to Turonian age, is a<br />
thin (approximately one metre) layer within the Scaglia Bianca<br />
Formation of the Umbria sequence of central Italy. It consists of<br />
black mudstones rich in organic matter, silty shales and beds of<br />
<strong>radiolaria</strong>n siltstones and fine sandstones. The abundance of organic<br />
matter reflects the anoxic conditions prevailing during its<br />
deposition.<br />
Several sections (Valle del Bottaccione, Valle della Contessa,<br />
Monte Petrano, Valle del Burano and Gola del Furlo) show that the<br />
Bonarelli Horizon includes a "lower" <strong>radiolaria</strong>n assemblage<br />
characterized by the presence of Novixitus mclaughlini, Thanarla<br />
pulchra, Holocryptocanium astiensis, Archaeodictyomitra sliteri,<br />
Pseudodictyomitra carpatica, and an "upper" assemblage where<br />
Alievium superbum is present in association with Crucella cachensis<br />
and Pseudoaulophacus putahensis. The transition between the<br />
"lower" and "upper" assemblages represents a faunal event that, on<br />
the basis of current knowledge of <strong>radiolaria</strong>n biostratigraphy,<br />
suggests a correlation with the Cenomanian-Turonian boundary.<br />
Matsuda, T. & Isozaki, Y. 1991. Well-documented<br />
travel history of Mesozoic pelagic chert in Japan; from<br />
remote ocean to subduction zone. Tectonics, 10/2, 475-499.<br />
The Mino-Tanba belt in southwest Japan, a segment of the<br />
Cordilleran-type orogenic chain of Jurassic east Asia, is composed<br />
mainly of a Middle-Upper Jurassic subduction-accretion complex in<br />
which Triassic and Lower Jurassic bedded <strong>radiolaria</strong>n cherts occur as<br />
large allochthonous units structurally interlayered with Middle-Upper<br />
Jurassic clastic rocks. High-resolution microfossil (conodont and<br />
<strong>radiolaria</strong>) research has identified very low average sedimentation<br />
rates of about 0.5 g/cm 2 /1000 yr in the chert units, similar to<br />
those of modern pelagic sediments accumulated in open ocean<br />
environments. Judging from the low average sedimentation rate, high<br />
purity of biogenic silica, long duration of continuous deposition (>50<br />
m.y.), and wide along-strike extent (>1000 km), the bedded<br />
<strong>radiolaria</strong>n cherts in the Mino-Tanba belt are best understood as<br />
ancient pelagic sediments that accumulated in open ocean<br />
environments; accordingly, the alleged origin in smaller marginal<br />
basins is untenable. Upward lithologic change from bedded chert to<br />
overlying siliceous mudstone in the uppermost portion of chert<br />
sequences suggests the gradual landward approach of the oceanic<br />
plate toward a trench. The tectonic interlayering of these cherts and<br />
coarse-grained terrigenous clastics is a secondary feature that was<br />
added through duplexing-underplating in the subduction zone. On the<br />
basis of the primary stratigraphy and field occurrence of Triassic<br />
bedded chert in the Mino-Tanba belt, newly proposed are an idealized<br />
oceanic plate stratigraphy and a generalized travel history of a<br />
Cordilleran-type bedded chert from its birth at a mid-oceanic ridge<br />
to its demise at a subduction zone.<br />
Matsuoka, A. 1991a. Early Jurassic <strong>radiolaria</strong>ns from the<br />
Nanjo Massif in the Mino Terrane, central Japan. Part 1.<br />
Tricolocapsa, Stichocapsa and Minocapsa, n. gen. Trans.<br />
Proc. palaeont. Soc. Japan, n. Ser., 161, 720-738.<br />
Well-preserved Early Jurassic <strong>radiolaria</strong>ns are obtained from a<br />
manganese band in the Nanjo Massif, Mino Terrane, central Japan.<br />
This paper is Part I of a serial descriptive work on an Early Jurassic<br />
<strong>radiolaria</strong>n fauna from the Nanjo Massif and deals with nassellarians<br />
which possess a constricted or closed distal end. One new genus,<br />
Minocapsa, is erected, and 9 new species and 2 new subspecies are<br />
described: Tricolocapsa minoensis, T. (?) megaglobosa, T. (?) fera,<br />
Stichocapsa plicata plicata, S. plicata semiplicata, S. elegans, S.<br />
biconica, S. nanjoensis, Minocapsa cylindrica and M. globosa.<br />
The fauna from the Nanjo Massif is very similar to that of the<br />
upper Archicapsa pachyderma Zone of Jurassic <strong>radiolaria</strong>n zones in<br />
Japan. The fauna is correlative with the lower Toarcian fauna in eastcentral<br />
Oregon, North America.<br />
Matsuoka, A. 1991b. Middle Jurassic <strong>radiolaria</strong>ns from the<br />
western Pacific. In: Proceedings of the International<br />
Symposium on Shallow Tethys. Eds.), vol. 3. Saito Ho-on<br />
Kai Special Publication, Sendai, Japan. pp. 163-173.<br />
Middle Jurassic <strong>radiolaria</strong>ns have been recovered from the<br />
western Pacific for the first time. The oldest faunas are assigned to<br />
the middle and upper Tricolocapsa conexa Zone, indicating a<br />
Bathonian/Callovian age. The faunas contain more than 30 species<br />
and are characterized by an abundance of small nassellarians with a<br />
constricted distal end. The faunas compare well with Tethyan faunas,<br />
and are especially similar to Japanese faunas.<br />
Minoura, K., Nakaya, S. & Takemura, A. 1991.<br />
Origin of manganese carbonates in Jurassic red shale, central<br />
Japan. Sedimentology, 38/1, 137-152.<br />
- 68 -<br />
Manganese carbonate deposits in Japanese Jurassic<br />
sedimentary rocks were studied petrogeochemically. The deposits<br />
are characteristically composed of spheroidal micronodules, up to 1<br />
mm in diameter, and always contain well-preserved <strong>radiolaria</strong>n<br />
shells. Chemical elemental composition and mineralogical<br />
characteristics indicate that the micronodules contain rhodochrosite<br />
in a mixed carbonate phase composition (Mn86.7-92.2Ca2.2-2.9Mg2.6- 6.7Fe2.6-5.6 )CO3. Carbon and oxygen isotope values, which range<br />
from —7.99 to —4.78‰ and —4.05 to 0.28‰ relative to PDB,<br />
respectively, suggest that the manganese carbonate was<br />
precipitated in a suboxic zone. The micronodules closely resemble<br />
agglutinated benthic foraminifera in shape. We suggest that<br />
agglutinated foraminiferal tests composed of <strong>radiolaria</strong>n shells<br />
accumulated selectively on the sediment surface during redeposition<br />
of bottom sediments and were replaced by manganese carbonate in<br />
suboxic diagenetic conditions of manganese reduction.<br />
Misík, M., Jablonsky, J., Ozvoldová, L. &<br />
Halásová, E. 1991. Distal turbidites with pyroclastic<br />
material in Malmian radiolarites of the Pieniny Klippen Belt<br />
(Western Carpathians). Geologica carpath., 42/6, 341-360.<br />
Acid and intermediary Upper Oxfordian volcanic material<br />
transported from distant centres (probably the Eastern Alps) by<br />
bottom currents (distal turbidites, or contourites) forms<br />
intercalations in radiolarites of the Klippen Belt. The study of<br />
<strong>radiolaria</strong>ns (U.A. 7-8 and U.A.9) and partly also of calcareous<br />
nanoplankton allowed to determine a wider-stratigraphic span of red<br />
<strong>radiolaria</strong>ns (Buwald Member) - minimally Upper Oxfordian—Lower<br />
Kimmeridgian. The correlation between the thicknesses of<br />
alternating silicite and pelite beds is insignificant (0.266). Fourteen<br />
types of <strong>radiolaria</strong>n preservation, various types of veinlets, the<br />
presence of spheroids and slide structures allow to reconstruct to a<br />
certain extent the processes of sedimentation and diagenesis.<br />
Mizutani, S. & Yao, A. 1991. Radiolarians and terranes:<br />
Mesozoic geology of Japan. Episodes, 14/3, 213-216.<br />
Nobody can understand the geology of Japan without the<br />
knowledge of <strong>radiolaria</strong>n biostratigraphy and the concepts of<br />
terranes. In the past decade, considerable research has been carried<br />
out on <strong>radiolaria</strong>n fossils, particularly those in the basement rocks<br />
of Paleozoic and Mesozoic ages. The results indicate that Jurassic<br />
formations are widespread and that they constitute an accretionary<br />
complex. After establishing a new series of <strong>radiolaria</strong>n fossil zones,<br />
we have reexamined the stratigraphy of the basement rocks and<br />
have recognized many tectonostratigraphic terranes in the Japanese<br />
Islands. Discussion on the tectonic history of the Mesozoic terrain is<br />
extended to that of eastern Asia in relation to accretion and<br />
dispersion processes.<br />
Molina-Cruz, A. 1991. Holocene palaeo-oceanography of<br />
the northern Iceland Sea, indicated by Radiolaria and sponge<br />
spicules. J. Quaternary Sci., 6/4, 303-312.<br />
The micropalaeontological analysis of 49 samples, from three<br />
box cores collected from the northern Iceland Plateau, indicates that<br />
<strong>radiolaria</strong>n and sponge remains are rare in glacial sediments but are<br />
common after deglaciation; mostly during the first half of the<br />
Holocene. Fluctuations in <strong>radiolaria</strong>n abundance, and the first<br />
occurrence of each of the species inhabiting the Iceland Sea at<br />
present, coincide with changes in oceanographic conditions that<br />
occurred during the Holocene<br />
Morley, J.J., Heusser, L.E. & Shackleton, N.J.<br />
1991. Late Pleistocene/Holocene <strong>radiolaria</strong>n and pollen<br />
record from sediments in the Sea of Okhotsk.<br />
Paleoceanography, 6/1, 121-131.<br />
In two cores with oxygen isotope stratigraphy from the<br />
southern Okhotsk Sea, marine pollen and siliceous microfauna record<br />
concurrent late glacial through Holocene variations in regional<br />
terrestrial and marine environments. Glacial vegetation around the<br />
southern Okhotsk basin, which resembles the present tundra/steppe<br />
of the northwest coast of this marginal sea, yields to spruce<br />
dominated boreal forests during the glacial/interglacial transition.<br />
Temperate forest components, such as oak, peak during the mid-<br />
Holocene. Decreasing oak accompanied by increasing spruce<br />
reflects the effect of global cooling on local vegetation during the<br />
last 4 kyr. Although the <strong>radiolaria</strong>n fauna in the Okhotsk Sea<br />
samples is similar to that present in the northwest Pacific, the<br />
dominant species in both regions differ. Concentrations of<br />
<strong>radiolaria</strong>ns are low in latest glacial samples, with higher<br />
concentrations occurring above and below this interval.<br />
Cycladophora davisiana, the dominant <strong>radiolaria</strong>n species in the<br />
majority of Holocene Okhotsk Sea sediments, is present at lower<br />
percentages in late glacial samples from our two sites. Thus, this<br />
species' Holocene/latest Pleistocene abundance pattern in Sea of<br />
Okhotsk sediments is the reverse of that recorded in high-latitude
Radiolaria 14 Bibliography - 1991<br />
open ocean sites. The combined marine pollen and <strong>radiolaria</strong>n<br />
records indicate changes in the Sea of Okhotsk's physical<br />
oceanographic conditions and surrounding vegetation during the late<br />
glaciaI which were associated with this region's response to global<br />
climate change.<br />
Motoyama, I. 1991. 3-2 Radiolaria. In: Preliminary<br />
results on Tansei-maru Cruise KT90-9 in Forearc Areas off<br />
Northern Tohoku and Hokkaido, and Sagami Bay, Japan.<br />
(Tsukawaki, S. & Nemoto, N., Eds.), vol. 38/1. Sci. Rep.<br />
Hirosaki Univ., pp. 61-62.<br />
Nagai, H. & Mizutani, S. 1991. Jurassic Radiolarians<br />
from Tsuzuya, Minokamo City, Central Japan. Bull. Nagoya<br />
Univ. Furukawa Mus., 7, 1-13. (in Japanese)<br />
Jurassic <strong>radiolaria</strong>ns extracted from siliceous shale exposed at<br />
Tsuzuya, Minokamo City, Gifu Prefecture. are briefly described. They<br />
range in age from the middle Jurassic to the lower part of the upper<br />
Jurassic, and are partly correlative with those of the Dictyomitrella<br />
(?) kamoensis-Pantanellium foveatum assemblage commonly found<br />
in the Mino terrane, central Japan. Geologically, however, it is worthy<br />
to note that the siliceous shale of the study area is much thicker<br />
than the other areas so far described despite of the same<br />
biostratigraphic horizon. This implies 1) the siliceous shale of the<br />
study area is more or less different in its sedimentary facies from<br />
that of the other areas, and is truly well developed and thicker, or 2)<br />
the siliceous shale is duplicated or triplicated owing to the structural<br />
deformation after the deposition. The present study is carried out to<br />
find a relationship between the <strong>radiolaria</strong>n assemblage and the<br />
sedimentary facies or geological structures, and it describes<br />
common species of the <strong>radiolaria</strong>ns found in the siliceous shale of<br />
the Mino terrane.<br />
Nakae, S. 1991. Latest Jurassic <strong>radiolaria</strong>ns from the<br />
Miyama area in the Tamba Terrane and their significance. J.<br />
geol. Soc. Japan, 97/5, 385-387. (in Japanese)<br />
Nelson, D.M., Ahern, J.A. & Herlihy, L.J. 1991.<br />
Cycling of biogenic silica within the upper water column of<br />
the Ross Sea. Marine Chem., 35, 461-476.<br />
We determined the distributions of biogenic particulate silica<br />
and dissolved silicic acid in the upper 80 m over the continental<br />
shelf of the southern Ross Sea, Antarctica, during two occupations<br />
of an east-west transect at 76°30'S in mid-January and early<br />
February 1990. There was a persistent (at least 3.5 weeks in<br />
duration) diatom bloom within a surface meltwater lens extending<br />
100-150 km seaward from the edge of the receding pack ice, with<br />
biogenic silica concentrations frequently exceeding 20 µmol l -1 in<br />
the upper 15 m. There were also other significant maxima in biogenic<br />
silica, with concentrations greater than 7 µmol l -1 at distances of<br />
250-500 km seaward of the ice edge. These maxima were<br />
apparently unrelated to meltwater effects.<br />
30<br />
Si tracer experiments to measure the production and<br />
dissolution rates of biogenic silica as a function of depth within the<br />
upper 50 m at three stations within the ice-edge diatom bloom<br />
indicate that the specific production rate (i.e. the rate per unit of<br />
biogenic silica present) ranged from 0.05 to 0.12 day- 1 (0.07-0.17<br />
doublings day -1 ). The resulting vertically integrated silica production<br />
rates ranged from 27 to 50 mmol m -2 day -1 , with a mean of 34.<br />
Vertically integrated rates of biogenic silica dissolution ranged from<br />
16 to 28 mmol m -2 day -1 , with a mean of 22, or 64% of the mean<br />
silica production rate. The mean resulting net rate of biogenic silica<br />
production within the bloom, 12 mmol m -2 day -1, leads to an<br />
estimated net annual silica production rate of 1.0 mol m -2 in the<br />
upper 50 m of the southwestern Ross Sea. A revised silica budget<br />
for the western Ross Sea, incorporating the most recent estimates<br />
of production, redissolution, accumulation in the sediments and<br />
efflux from the sea-- bed, indicates that virtually all silica exported<br />
from the upper 50 m must reach the sea-floor unless advective<br />
transport from the east is significant.<br />
Nigrini, C. 1991. Composition and biostratigraphy of<br />
<strong>radiolaria</strong>n assemblages from an area of upwelling<br />
(Northestern Arabian Sea, Leg 117). In: Proceedings of the<br />
Ocean Drilling Program, Scientific Results. (Prell, W.J.,<br />
Nitsuma, N. et al., Eds.), vol. 117. College Station, TX<br />
(Ocean Drilling Program), pp. 89-126.<br />
Significant numbers of <strong>radiolaria</strong>ns ranging in age from late<br />
middle Miocene to Recent were recovered from six sites drilled on<br />
the Oman margin and Owen Ridge. Sparse faunas were recovered<br />
from five additional sites on the Oman margin and one site on the<br />
Indus Fan. Detailed range charts and biozonations are presented for<br />
most sites. The <strong>radiolaria</strong>n assemblages are peculiar in that<br />
- 69 -<br />
numerous common tropical forms, some of which are biomarkers, are<br />
absent or very rare. In addition, some species not usually found in<br />
tropical assemblages are present. These forms, indicative of<br />
upwelling conditions, fall into three categories: (I) endemic upwelling:<br />
species endemic to upwelling and not previously described from the<br />
Indian Ocean; (2) displaced temperate: temperate forms not usually<br />
found in tropical waters; and (3) enhanced tropical: tropical forms<br />
which are more abundant and/or robust in areas of upwelling.<br />
Comparison of the Oman margin/Owen Ridge fauna with that<br />
recovered from the Peru margin upwelling area (ODP Leg 112)<br />
suggests that the assemblage may be globally diagnostic of<br />
upwelling conditions.<br />
The onset of upwelling is marked by the appearance of siliceous<br />
biota at about 11.9 Ma, and there is some indication of a decrease in<br />
the strength of the upwelling signal at about 9.6 Ma. A strong pulse<br />
in, or strengthening of, the upwelling mechanism is indicated by a<br />
marked fauna change at 4.7 Ma. There is a weaker signal, implying a<br />
change in upwelling conditions, at about 1.5 Ma.<br />
Nöthig, E.M. & Gowing, M.M. 1991. Late winter<br />
abundance and distribution of phaeodarian <strong>radiolaria</strong>ns, other<br />
large protozooplankton, and copepod nauplii in the weddell<br />
Sea, Antarctica. Marine Biol., 111, 473-484.<br />
Large protozooplankton ( 400 µm) phaeodarian <strong>radiolaria</strong>ns;. contributed more than<br />
98 % of the carbon h the large protozooplankton fraction; large<br />
protozooplankton were approximately 38 % of the total<br />
protozooplankton carbon during the late winter under the close pack<br />
ice in the upper 250 m. This indicates that large protozooplankton<br />
may be an important food source for small particle-feeding<br />
zooplankton in the upper 250m, and a modest food source down to<br />
l000m.<br />
Phaeodarian species distributions showed a distinct vertical<br />
pattern: Challengeron bicorne, Protocystis tridens, Phaeodina<br />
antarctica and Cannosphaera antarctica were most abundant in the<br />
upper water column; Protocystis micropelecus. Protocystis<br />
triangularis, and the families Aulacanthidae, Aulosphaeridae, and<br />
Coelodendridae were most abundant between 100 and 500 m; and<br />
Protocystis harstoni, Euphysetta sp., and Porospathis sp. were<br />
dominant in the deeper water. Except for spumellarian and<br />
nassellarian <strong>radiolaria</strong>ns all other protozooplankton (foraminiferans,<br />
thecate dinoflagellates, tintinnids) were most abundant in the upper<br />
250 m. This vertical pattern changed slightly from west to east. The<br />
horizontal variation showed a western, central and eastern pattern<br />
most probably due to the differing regional hydrography.<br />
Feeding ecology of the dominant species of phaeodarians was<br />
examined using transmission electron microscopy of contents of<br />
feeding vacuoles. The 58 specimens were trophic generalists, having<br />
consumed a variety of detrital material, autotrophic and<br />
heterotrophic protozoans, and bacteria. Silica fragments and<br />
amorphous material dominated vacuole contents. Several lines of<br />
evidence, including the similarity of vacuole contents of specimens<br />
from 3 depth zones, suggest that phaeodarians in late winter may<br />
have fed on organic aggregates.<br />
Okada, H., Tarduno, J.A., Nakaseko, K.,<br />
Nishimura, A. & Sliter, W.V. 1991. Reexamination of<br />
the age of the uppermost sequence of the Sorachi Group in its<br />
type area, Hokkaido, Japan. Mem. Fac. Sci., Kyushu Univ.,<br />
Series D (Earth planet. Sci.), 27/1, 1-13.<br />
The Sorachi Group of central Hokkaido is characterized by<br />
hemipelagic sediments and ophiolitic rock associations. To<br />
determine the precise age of the upper Sorachi Group, a key unit in<br />
the geotectonic evolution of Hokkaido, <strong>radiolaria</strong>n fossil<br />
assemblages have been studied. The results indicate that the upper<br />
Sorachi Group may be Albian in age, much younger than previously<br />
believed. This age is similar to that obtained for the youngest<br />
pelagites of the Nikoro Group of the Tokoro Belt, eastern Hokkaido,<br />
although the paleoenvironmental and paleogeographic settings of the<br />
two groups may well have differed.<br />
Queguiner, B., Treguer, P. & Nelson, D.M. 1991.<br />
The production of biogeneic silica in the Weddell and Scotia<br />
Seas. Marine Chem., 35, 449-459.
Bibliography - 1991 Radiolaria 14<br />
During the EPOS leg 2 cruise (European Polarstern Study,<br />
November 1988-January 1989), the production rate of biogenic<br />
silica in the euphotic zone was measured by the 30 Si method at<br />
stations in the Scotia and Weddell Seas. The highest integrated<br />
production rates were observed in the Scotia Sea (range: 11.2-20.6<br />
mmol Si m -2 day -1 ) . the marginal ice zone of the Weddell Sea<br />
exhibiting somewhat lower values ( range: 6.0- 20.0 mmol Si m -2<br />
day -1 ).<br />
Our results demonstrate that as far as biogenic silica<br />
production is concerned the marginal ice zone of the Weddell Sea is<br />
considerably less productive than that of the Ross Sea. Our results<br />
also indicate that the water of the Antarctic Circumpolar Current<br />
(ACC) could be more productive in late spring and early summer than<br />
at the beginning of spring. Possible reasons for the differences<br />
among the three subsystems (Ross Sea, Weddell Sea and ACC) are<br />
discussed.<br />
Pujana, I. 1991. Pantanelliidae (Radiolaria) from the<br />
Tithonian of the Vaca Muerta Formation, Neuquén, Argentina.<br />
N. Jb. Geol. Paläont., Abh., 180/3, 391-408.<br />
Radiolaria from limestones and mudstones of the Vaca Muerta<br />
Formation of Neuquen (Argentina) correlative with the<br />
Windhauseniceras internispinosum Zone of late Middle Tithonian age<br />
represent the first systematic documentation of Late Jurassic<br />
Radiolaria from the Andes. The representatives of the Pantanelliidae<br />
are discussed in detail and include two new species.<br />
Reid, P.C., Turley, C.M. & Burkill, P.H. 1991.<br />
Protozooa and their role in marine processes. NATO ASI<br />
Conference Series, Series IV Marine Sciences, Springer-<br />
Verlag G25, 506 p.<br />
Roeser, H.A. 1991. Age of the crust of the southeast Sulu<br />
Sea basin based on magnetic anomalies and age determined at<br />
Site 768. In: Proceedings of the Ocean Drilling Program,<br />
Scientific Results. (Silver, E.A., Rangin, C., Von Breymann,<br />
M.T. et al., Eds.), vol. 124. College Station, TX (Ocean<br />
Drilling Program), pp. 339-343.<br />
Magnetic measurements from marine and airborne geophysical<br />
surveys show east-northeast-striking lineated anomalies in the<br />
southeast Sulu Sea Basin. A seafloor spreading model was developed<br />
that indicates an age of 15 Ma for the oceanic crust at Ocean<br />
Drilling Program Site 768. Radiolarian ages near the base of the<br />
sedimentary sequence at Site 768 give an approximate age of 17<br />
Ma. The age discrepancy might be due to the inaccuracies inherent in<br />
both methods and to sediment transportation by turbidites.<br />
According to the magnetics model, it is likely that the Sulu Sea<br />
Basin started to open at 30-35 Ma (early Oligocene) with 0.6 cm/yr<br />
half-spreading rate. Spreading continued until at least 10 Ma (early<br />
upper Miocene). Most of the oceanic crust is already subducted.<br />
Sashida, K. 1991. Early Triassic <strong>radiolaria</strong>ns from the<br />
Ogamata Formation, Kanto Mountains, central Japan; Part 2.<br />
Trans. Proc. palaeont. Soc. Japan, n. Ser., 161, 681-696.<br />
Chert beds of the Ogamata Formation exposed in the upper<br />
reaches of the Nakatsugawa River, Kanto Mountains, yield abundant<br />
Early Triassic <strong>radiolaria</strong>ns. A part of this <strong>radiolaria</strong>n fauna including<br />
the spicular type Palaeoscenidiidae was already described by the<br />
present author. As an addition to the study of this fauna, several<br />
newly discriminated Spumellaria and Nasellaria are described in this<br />
paper. The families Palaeoscenidiidae with a latticed shell,<br />
Pantanellidae, and Sponguriidae are included in the Spumellarians.<br />
The families Eptingiidae having a spumellarian-like affinity and<br />
Acanthodesmiidae are classified as Nassellaria in this study. Five<br />
new species, Archaeothamnulus okuchichibuensis, Parentactinia<br />
virgata, Pactarentinia koikei, Pantanellium ? virgeum, and<br />
Spongostephanidium longispinosum, are proposed herein.<br />
Sashida, K. & Tonishi, K. 1991. An Upper Permian<br />
coiled <strong>radiolaria</strong>n from Itsukaichi, central Japan.<br />
Micropaleontology, 37/1, 86-94.<br />
Well-preserved and abundant <strong>radiolaria</strong>ns having a coiled<br />
internal skeleton were recovered from an Upper Permian chert block<br />
embedded in the Unazawa Formation located in Kashiwara, Itsukaichi<br />
Town, Tokyo Prefecture, central Japan. This unusual species of<br />
Radiolaria is characterized by its more complicated streptospiral<br />
shell compared with those species of Radiolaria with simple spirals<br />
along one coiling axis. In the present study, the authors propose the<br />
new Family Grandetorturiidae in the Suborder Spumellaria Ehrenberg<br />
and describe one new genus and species, Grandetortura nipponica<br />
Sashida and Tonishi.<br />
- 70 -<br />
Sashida, K. & Yatsugi, M. 1991. Note on the middle<br />
Chichubu Belt of the Kanto Mountains, central Japan. Annu.<br />
Rep. Inst. Geosci., Univ. Tsukuba, 17, 56-62.<br />
During the course of our study in the Middle Chichibu Belt,<br />
Kanto Mountains, we discriminated abundant and well-preserved<br />
Early Jurassic <strong>radiolaria</strong>ns from the argillaceous rock facies of the<br />
Kawai and Raidenyama Formations. In this paper, we describe the<br />
occurrence of the Early Jurassic <strong>radiolaria</strong>ns from the above<br />
mentioned two formations and briefly summarize the geology of the<br />
Middle Chichibu Belt of the Kanto Mountains by collating the present<br />
results with previously reported facts. Paleontological works will be<br />
presented in another paper.<br />
Savary, J. & Guex, J. 1991. BioGraph: un nouveau<br />
programme de construction des corrélations<br />
biochronologiques basées sur les associations unitaires. Bull.<br />
Soc. vaud. Sc. nat., 80/3, 317-340.<br />
A new program for constructing Unitary Associations (U.A.) and<br />
biochronologic correlations is described here. This program, named<br />
BIOGRAPH, is based on recent developments on the U.A. method. It is<br />
designed to establish discrete biochronologic relative time scales<br />
calculated on any IBM PC or compatible microcomputer in very short<br />
time.<br />
Scherer, R.P. 1991a. Radiolarians of the Celebes Sea, Leg<br />
124, Sites 767 and 770. In: Proceedings of the Ocean Drilling<br />
Program, Scientific Results. (Silver, E.A., Rangin, C., Von<br />
Breymann, M.T. et al., Eds.), vol. 124. College Station, TX<br />
(Ocean Drilling Program), pp. 345-357.<br />
Two sites were drilled in the Celebes Sea as part of Ocean<br />
Drilling Program Leg 124; Site 767 and Site 770. Radiolarians are<br />
preserved in Paleogene pelagic claystones with minor occurrences in<br />
certain Neogene successions. The brown clays that immediately<br />
overlie basalt at both sites contain <strong>radiolaria</strong>ns of the late middle<br />
Eocene Podocyrtis chalara Zone. Late Eocene <strong>radiolaria</strong>ns are not<br />
found, due to dissolution and probable hiatus. The Oligocene is<br />
represented by the Theocyrtis tuberosa and Dorcadospyris ateuchus<br />
Zones. Oligocene sediments are strongly dominated by abundant and<br />
diverse <strong>radiolaria</strong>ns of the Tristylospyris/Dorcadospyris lineage.<br />
Preservation of Paleogene <strong>radiolaria</strong>n assemblages ranges from good<br />
to very poor. Late Miocene <strong>radiolaria</strong>ns of the Didymocyrtis<br />
antepenultima Zone are found only in Site 770. Other Neogene<br />
sediments are barren of <strong>radiolaria</strong>n remains, with the exception of<br />
latest Pleistocene and Holocene sediments.<br />
Scherer, R.P. 1991b. Miocene <strong>radiolaria</strong>ns of the Sulu<br />
Sea, Leg 124. In: Proceedings of the Ocean Drilling Program,<br />
Scientific Results. (Silver, E.A., Rangin, C., Von Breymann,<br />
M.T. et al., Eds.), vol. 124. College Station, TX (Ocean<br />
Drilling Program), pp. 359-368.<br />
Radiolarians are sporadic in sediments collected in the Sulu Sea<br />
during ODP Leg 124. Due to the generally poor preservation and low<br />
abundance of <strong>radiolaria</strong>ns in Sulu Sea sediments, no biostratigraphic<br />
datums are well defined, although three <strong>radiolaria</strong>n zones are<br />
identified. Most samples containing <strong>radiolaria</strong>ns are pelagic or<br />
hemipelagic clays with varying proportions of volcanic ash. Detailed<br />
analysis of Sulu Sea <strong>radiolaria</strong>ns was limited to Miocene<br />
successions. Pliocene and Quaternary occurrences of <strong>radiolaria</strong>ns<br />
were noted but have not been zoned.<br />
The late middle Miocene of Sites 769 and 771 is represented<br />
by an assemblage of <strong>radiolaria</strong>ns (Diartus petterssoni Zone) that is<br />
entirely replaced by massive pyrite. This type of preservation<br />
develops only under anoxic conditions. The development of<br />
widespread anoxia in Sulu Sea waters in the late middle Miocene was<br />
probably the result of hydrologic isolation of basin waters, and may<br />
be associated with eustatic sea level fall over the silled basin.<br />
Upper lower Miocene pelagic and hemipelagic sediments that<br />
overlie pyroclastics and basalt flows in the Sulu Sea sites contain<br />
moderately to very poorly preserved <strong>radiolaria</strong>ns of the Calocycletta<br />
costata Zone. A thin unit of marine claystone was recovered from<br />
between the thick pyroclastics and basement rocks at Site 768.<br />
Radiolarians present in these claystones are rare and very poorly<br />
preserved. This <strong>radiolaria</strong>n assemblage probably represents the C.<br />
costata Zone, although very poor preservation and low abundance<br />
make this interpretation equivocal. The <strong>radiolaria</strong>n zones identified<br />
constrain the age of basin formation to late early Miocene or earlier.<br />
Spaulding, S.A., Bloemendal, J., Hayashida, A.,<br />
Hermelin, J.O.R., Kameo, K., Kroon, D.,<br />
Nigrini, C.A., Sato, T., Steens, T.N.F.,<br />
Takayama, T. & Troelstra, S.R. 1991.<br />
Magnetostratigraphic and biostratigraphic synthesis, Leg
Radiolaria 14 Bibliography - 1991<br />
117, Arabian Sea. In: Proceedings of the Ocean Drilling<br />
Program, Scientific Results. (Prell, W.J., Nitsuma, N. et al.,<br />
Eds.), vol. 117. College Station, TX (Ocean Drilling<br />
Program), pp. 127-145.<br />
During the late early Miocene to early middle Miocene, the Owen<br />
Ridge was uplifted to a sufficient height as to be above the realm of<br />
turbidite deposition. Monsoonal-induced upwelling appears to have<br />
been initiated during the Miocene. On the Oman Margin, the effect of<br />
upwelling on the microplankton was established by the middle<br />
Miocene. However, the effects of upwelling on the Owen Ridge region<br />
were not realized until later, in the early late Miocene. A transition in<br />
the upwelling regime took place between the Pliocene and<br />
Pleistocene. While the Miocene and Pliocene sediments are<br />
dominated by the siliceous component, the Pleistocene sediments<br />
seem to be dominated by the calcareous component.<br />
Spero, H.J. & Angel, D.L. 1991. Planktonic<br />
sarcodines: microhabitat for oceanic dinoflagellates. J.<br />
Phyc., 27/2, 187-195.<br />
Two morphologically distinct species of free-swimming<br />
dinoflagellates belonging to the genus Gyrodinium utilize the spine<br />
and rhizopodial environments of planktonic foraminifera and colonial<br />
<strong>radiolaria</strong> as microhabitats. Up to 84% of the sarcodines examined<br />
in a given population were associated with these dinoflagellates at<br />
densities up to 20,000 cells per sarcodine in some <strong>radiolaria</strong>n<br />
colonies. Both dinofagellate species possess chloroplasts, indicating<br />
they are capable of autotrophy. 14 C-labelling experiments with the<br />
<strong>radiolaria</strong>n-associated dinofagellate demonstrate that it can take up<br />
inorganic carbon under both light and dark conditions.<br />
Ultrastructural evidence suggests the foraminiferal dinoflagellate<br />
may be capable of phagotrophy. Hence, these algae should be<br />
considered mixotrophs. An unusual cytoplasmic extension used for<br />
attachment and possibly feeding occurs in the foraminiferalassociated<br />
Gyrodinium and is documented with electron microscopy.<br />
Ultrastructural examination suggests this organelle may be<br />
hydrostatically controlled and may be an extension of the sac<br />
pusule.<br />
Swanberg, N.R. & Caron, D.A. 1991. Patterns of<br />
sarcodine feeding in epipelagic oceanic plankton. J.<br />
Plankton Res., 13/2, 287-312.<br />
The range of in situ prey composition was determined in marine<br />
planktonic acantharia, foraminifera and <strong>radiolaria</strong> collected by<br />
divers, and quantitatively compared with the prey available, as<br />
determined by surface plankton hauls on cruises in the Florida<br />
Current, Gulf Stream and Sargasso Sea. A relatively large percentage<br />
of the sarcodines (60% of acantharia, 48% of foraminifera and 46%<br />
of <strong>radiolaria</strong>) had no detectable prey. Of those which had fed on<br />
identifiable prey, there was considerable overlap between sarcodine<br />
species in the types of prey captured. Nevertheless, some<br />
partitioning of food resources was evident. Foraminifera consumed<br />
greater numbers of diatoms and copepods than other prey types,<br />
<strong>radiolaria</strong> consumed more tintinnids and mollusc larvae and<br />
acantharia consumed mostly tintinnids. Copepods and their nauplii<br />
dominated the biomass consumed for all three groups, though<br />
mollusc larvae were significant for both acantharia and <strong>radiolaria</strong>.<br />
The results of parameteric univariate statistical analyses carried<br />
out on each major predator group and multivariate analysis on a<br />
species-by-species basis confirmed that there was evidence for<br />
some partitioning of prey resources among the major sarcodine<br />
predators. The partitioning appeared to follow primarily<br />
morphological rather than taxonomic criteria, however, and may have<br />
been at least partially a mechanical effect.<br />
Takahashi, K. 1991a. Radiolaria: Flux, Ecology, and<br />
Taxonomy in the Pacific and Atlantic. In: Ocean Biocoenosis<br />
Series. (Honjo, S., Eds.), vol. 3. Woods Hole Oceanographic<br />
Institution, Woods Hole, Massachusetts. pp. 303.<br />
Radiolarians settling through the oceanic water column were<br />
recovered from three stations (western tropical Atlantic, Station E;<br />
central tropical Pacific, Station P1 ; and Panama Basin, Station PB)<br />
using PARFLUX sediment traps in moored arrays at several depths.<br />
The taxonomic diversity of the <strong>radiolaria</strong>n assemblages in the<br />
sediment traps was very high. A total of 420 taxa (including 23 new<br />
taxa) were found at the three stations; of these 208 taxa were<br />
found at Station E. The polycystine <strong>radiolaria</strong>ns generally reach the<br />
sea floor with little change in abundance or species composition,<br />
although slight skeletal dissolution occurs during their descent<br />
through the water column. The phaeodarian <strong>radiolaria</strong>ns, on the other<br />
hand, are largely dissolved within the water column; only a few<br />
species reach the sea-floor and these dissolve rapidly at the<br />
sediment-water interface. Most <strong>radiolaria</strong>n skeletons sink as<br />
individuals through deep water columns without being incorporated<br />
into large biogenic aggregates. Because significant numbers of<br />
nassellarian and phaeodarian species are deep-water dwelling forms,<br />
- 71 -<br />
the diversity of <strong>radiolaria</strong>ns increases with increasing depth in the<br />
mesopelagic zone.<br />
The vertical flow of the total <strong>radiolaria</strong>ns arriving at the trap<br />
depths (in x10 3 individuals/m 2 /day) ranged from 16-24 at Station<br />
E, 0.6-17 at Station P1 , and 29-53 at Station PB. On the average<br />
25% and 69% of the total <strong>radiolaria</strong>n flux is transported by<br />
Spumellaria and Nassellaria, respectively, while 5% is carried by<br />
Phaeodaria. The supply of <strong>radiolaria</strong>n silica (mg SiO2 /m 2 /day) to<br />
each trap depth ranged from 2.5-4.0 at Station E, 0.9-3.2 at Station<br />
P l , and 5.7-10.4 at Station PB. The Radiolaria appear to be a<br />
significantly large portion of the SiO2 flux in the > 63 µm size<br />
fraction and thus play an important role in the silica cycle. When the<br />
<strong>radiolaria</strong>n fluxes at the three stations are compared with Holocene<br />
<strong>radiolaria</strong>n accumulation rates in the same areas it became apparent<br />
that several percent or less of the fluxes are preserved in the<br />
sediment in all cases and the rest must be dissolved on the seafloor.<br />
Takahashi, K. 1991b. Mineral flux and biogeochemical<br />
cycles of marine planktonic Protozoa - session summary. In:<br />
Protozoa and their role in marine Processes. (Reid, P.C.,<br />
Turley, C.M. & Burkill, P.H., Eds.), NATO ASI Conference<br />
Series, Series IV Marine Sciences vol. G25. Springer-Verlag,<br />
Berlin/Heidelberg. pp. 347-359.<br />
Since the first NAT0-ASI Workshop on the Ecology of Marine<br />
Planktonic Protozoa was held in Villefranch-sur-mer in 1981, a<br />
marked advance has been made in the study of shell-bearing marine<br />
planktonic protozoa. In particular, vertical flux measurements using<br />
sediment traps (e.g. Deuser et al. 1981, Takahashi and Honjo 1981,<br />
Reid 1982) have contributed to the understanding of marine<br />
ecosystems, and the material balance, and seasonal, interannual,<br />
and spatial distribution of plankton (e.g. Thunell et al. 1983, Be et al.<br />
1985, Smetacek 1985, Pisias et al. 1986, Takahashi 1986, 1987a<br />
b c, Thunell and Honjo 1987, Leventer and Dunbar 1987, Gersonde<br />
and Wefer 1987, Sancetta and Calver 1988.<br />
Fluxes of biogenically precipitated minerals in the oceans,<br />
largely represented by biogenic silica and calcium carbonate, are<br />
important in global ecosystems. Both of the above minerals are<br />
produced in large quantities in marine environments and are partially<br />
entered into the geologic record. It should be noted that oceanic<br />
upper layer biological productivity has changed with time in the past:<br />
for example, significantly different productivity levels from those of<br />
the present day occurred in parts of the world oceans during the<br />
maximum extent of the last glacial age (Sundquist and Broecker<br />
1985). Environmental shifts will likely cause changes not only in<br />
productivity but also in the preservation of sedimenting biogenic<br />
minerals to the sea-floor (Andersen and Malahoff 1977). Between<br />
production and preservation there is some remineralization of<br />
material into the water. The degree of remineralization will cause<br />
changes in productivity in a feed back manner.<br />
Takeuchi, M., Saito, M. & Takizawa, F. 1991.<br />
Radiolarian fossils obtained from conglomerate of the Tetori<br />
Group in the upper reaches of the Kurobegawa River, and its<br />
geologic significance. J. geol. Soc. Japan, 97/5, 345-356.<br />
(in Japanese)<br />
The Tetori Group in the upper reaches of the Kurobegawa River<br />
is divided into three subgroups, the Middle to Late Jurassic Kuzuryu<br />
Subgroup; the late Late Jurassic (?) to early Early Cretaceous<br />
Itoshiro Subgroup, and the late Early Cretaceous Akaiwa Subgroup.<br />
The Tetori Group consists largely of conglomerate and sandstone<br />
with minor mudstone. Late Carboniferous to Middle Permian<br />
<strong>radiolaria</strong>ns and late Middle Permian to Late Permian <strong>radiolaria</strong>ns<br />
were obtained from the lower conglomerate member. Late Middle<br />
Permian to early Late Permian, late Middle Triassic, and Jurassic<br />
<strong>radiolaria</strong>n fossils were obtained from the uppermost conglomerate<br />
member. The influx of clastic materials from the accretionary<br />
complex suggests that a part of the accretionary complex was<br />
already uplifted and eroded in the late Neocomian.<br />
Thein, M., Ogawa, Y. & Akiyama, T. 1991. Finding<br />
of Cretaceous <strong>radiolaria</strong>ns from the block of sheared<br />
olistostrome in the southern part of the Shimanto Belt near<br />
the Ashizumi Cape, Kochi prefecture. J. geol. Soc. Japan,<br />
97/8, 667-669.<br />
The Paleogene succession of the southern part of the Shimanto<br />
Belt in the Hata Peninsula, Kochi Prefecture, is composed of two<br />
formations, namely the Kurusuno Formation (Katto & Mitsui, 1976)<br />
and the Shimizu Formation (Katto, 1960). The two are fault bounded,<br />
whereas the Shimizu Formation is unconformably overlain by the<br />
Lower Miocene Misaki Group (Kimura, 1985). Matsuo (1980)<br />
reported plant fossils having the range from Oligocene to Middle<br />
Miocene in age near Tosashimizu City. Kimura (1985) also found<br />
molluscan fossils on the footpath from Iburi Village leading to
Bibliography - 1991 Radiolaria 14<br />
Yokomichi Village. Matsumaru & Kimura (1989) found the Eocene<br />
larger foraminifera from the gray tuffaceous mudstone of the<br />
Shimizu Formation at Takahata Village, but the present authors<br />
consider the location belongs to the Kurusuno Formation from the<br />
view point of lithologic characteristics. The boundary between the<br />
two formations is now considered to be further south than the<br />
original boundary of Kimura (1985). They also found Eocene larger<br />
foraminifera from the Shimizu Formation at Yokomichi, South of<br />
Tosashimizu City. Judging from the larger foraminifera, Kimura<br />
(1985) interpreted the age of the Shimizu Formation corresponding<br />
to the age ranging from Late Eocene to Late Oligocene, and<br />
correlated the formation to the Nichinan Group in Miyazaki<br />
Prefecture. He interpreted that the Shimizu Formation is an originally<br />
submarine slide deposits and may contain older clasts and blocks<br />
ranging from Cretaceous to Eocene from an uplifted accreted<br />
terrane.<br />
On the other hand, we found the Late Oligocene or possible<br />
Early Miocene larger foraminifera (Nephrolepidolina morgani and<br />
Spiroclypeus sp., determined by Matsumaru, personal<br />
communication, 1990) from the volcanic pebble-bearing mudstone<br />
exposed along the coast line of the southern part of the Ohki beach.<br />
Detailed studies are now held, but we might therefore suggest most<br />
of the Shimizu Formation is of Oligocene to possible Early Miocene<br />
age, and includes some older Cretaceous blocks described here.<br />
Fossils had not previously been found from the deformed sediments<br />
around Tsuro, the south- ernmost part of the Shimizu Formation near<br />
Ashizuri Cape, where we found Late Cretaceous <strong>radiolaria</strong>ns<br />
reported here (Figs. 1 and 2). The fossils were collected from the<br />
mud dominated part of the clast of sandy turbidite within the pebbly<br />
mudstone (Fig. 3). This clast is fault bounded so that its<br />
stratigraphic position is unknown anywhere in this locality.<br />
Tipper, H.W., Smith, P.L., Cameron, B.E.B.,<br />
Carter, E.S., Jakobs, G.K. & Johns, M.J. 1991.<br />
Biostratigraphy of the Lower Jurassic formations of the<br />
Queen Charlotte Islands, British Columbia. In: Evolution and<br />
Hydrocarbon Potential of the Queen Charlotte Basin, British<br />
Columbia. Eds.), vol. 90-10. Geological Survey of Canada,<br />
Paper, pp. 203-235.<br />
The Lower Jurassic strata of Queen Charlotte Islands have been<br />
divided into five lithologically distinct formations, namely: the<br />
Sandilands Formation of the Kunga Group and the Ghost Creek,<br />
Fannin, Whiteaves, and Phantom Creek formations of the Maude<br />
Group. The Rennell Junction unit is abandoned as a formation and the<br />
beds included within a redefined Fannin Formation.<br />
Macrofossils, particularly ammonites, and microfossils, notably<br />
Radiolaria, Foraminifera, Ostracoda, and ichthyoliths, are abundant,<br />
generally well-preserved, reasonably diverse, and are found, to a<br />
degree, in all formations. The record suggests a complete Lower<br />
Jurassic sequence with few, if any, hiatuses of consequence. The<br />
Pliensbachian ammonite zonation for North America is defined by<br />
stratotype and reference sections in Skidegate Inlet. Toarcian<br />
Radiolaria likewise have been zoned. The biostratigraphic studies of<br />
all faunas has as a goal, zonations based on many faunas and a<br />
satisfactory correlation of these schemes. Important macrofossils<br />
and microfossils are illustrated and zones and faunal assemblages<br />
have been described. The importance of fossils to mappers and<br />
stratigraphers and the application of these data to an understanding<br />
of paleogeography and tectonics is emphasized.<br />
Tonielli, R. 1991. Associazioni a radiolari dei "Calcari e<br />
Marne a Posidonia del Monte Terminilletto (RI).<br />
Paleopelagos, 1, 18-37.<br />
An Aalenian-Bajocian assemblage referred to the "Hsuum<br />
hisuikyoensis" zone (Hori, 1990) and to the range between 6 and 7<br />
zones defined by Carter (1988) is recognized in the "calcari e<br />
marne a Posidonia" Auct. of the Terminilletto (Ri) sequence; this<br />
assemblage testifies for the first time, even in the Central Italy, the<br />
presence of Middle Jurassic.<br />
Treguer, P. & Van Bennekom, A.J. 1991. The annual<br />
production of biogenic silica in the Antarctic Ocean. Marine<br />
Chem., 35, 477-487.<br />
The total annual production of biogenic silica (BSi) of the<br />
Antarctic Ocean is estimated at about 50 tera (T= 10 12 ) mol Si.<br />
This flux is calculated using available direct measurements of<br />
integrated silicic acid uptake rates, indirect estimates from field<br />
distribution of orthosilicic acid in austral winter compared with that<br />
in austral summer and/or after conversion of 14 C primary<br />
production using appropriate Si/C mole ratios measured for the four<br />
Antarctic subsystems: the Polar Front Zone, the Permanently Open<br />
Ocean Zone, the Seasonal Ice Zone, and the continental shelves and<br />
coastal zones. We show that most of the total production of BSi<br />
occurs in the surface layers of the Permanently Open Ocean Zone<br />
- 72 -<br />
and in the Seasonal Ice Zone, the contribution of the coastal areas<br />
being less relevant. Our results fit well with the previously described<br />
distributions of the net accumulation rates of opal in Antarctic<br />
abyssal and coastal sediments. The mean ratio of net opal<br />
accumulation at the sea-bed to the net production of BSi in the<br />
surface layer of the Antarctic Ocean is about 15%.<br />
Tsutsumi, A. 1991. Re-examination of stratigraphy and<br />
geological structure of the upper Paleozoic formations in the<br />
Ibara City, southwestern Okayama Prefecture. J. geol. Soc.<br />
Japan, 97/3, 197-216. (in Japanese)<br />
The Maizuru Belt and the Ultra-Tamba Belt are ENE-WSW<br />
trending structural belts which stretches from Kyoto Prefecture to<br />
the middle part of Okayama Prefecture. The surveyed area is<br />
situated at the westward extension of these structural belts. The<br />
Paleozoic group which crops out in the area is divided into three E-W<br />
trending zones, which are juxtaposed one another bounded by faults.<br />
The constituent strata of each zone are newly named the Saya,<br />
Shimoshigi and Hiehara Formations. The Saya Formation, more than<br />
500 m thick, is composed chiefly of slate with subordinate amounts<br />
of chert laminite and acidic and basic volcanic rocks. Most of these<br />
rocks are fissile due to the development of slaty cleavage. The<br />
Shimoshigi Formation, approximately 750 m thick, is subdivided into<br />
the lower and upper members; the former is composed mainly of<br />
basic volcanic rock and the latter of slate and alternating beds of<br />
slate and sandstone with subordinate coglomerate. The slate is<br />
characterized by a well-developed slaty cleavage. Radiolarian<br />
assemblages indicate that the upper member is Middle to Early<br />
Permian in age. The Hiehara Formation, more than 2000 m thick, is<br />
also subdivided into the lower and upper members. The lower member<br />
is composed of slate, pebbly slate, acidic and basic volcanic rocks<br />
with minor amounts of chert and red slate, while the upper member<br />
consists mainly of basic volcanic rock Based on analysis of<br />
structural elements, such as slaty cleavage, lineation and fold axis,<br />
three deformation stages are recognized in the structural<br />
development of the Saya and the Shimoshigi Formations and two<br />
deformation stages of the Hiehara Formation. During the first<br />
deformation stage, closed to tight folds with an axial plane slaty<br />
cleavage were formed. During the subsequent second stage of<br />
deformation open folds were formed. In the Saya and Shimoshigi<br />
Formation the second deformation is associated with formation of<br />
crenulation cleavages. Then the Saya and Shimoshigi Formations<br />
underwent the third deformation process characterized by kink folds<br />
that are locally superposed on the earlier structures.<br />
Ujiie, H. & Oba, T. 1991. Geology and Permo-Jurassic<br />
Radiolaria of the Iheya Zone, Innermost Belt of the Okinawa<br />
Islands region, middle Ryukyu island arc, Japan. Part 1.<br />
Geology and Permian Radiolaria. Part 2 Mesozoic Radiolaria<br />
and geological structures. Bull. College Sci., Univ. Ryukyus,<br />
51, 35-89.<br />
Umeda, M. 1991. Clastic dike in the Jurassic sequence in<br />
the western part of the Nanjo Massif, the Mino terrane,<br />
central Japan. In: Prof. Miura, S. - Memorial Volume. Eds.).<br />
pp. 89-95. (in Japanese)<br />
Vishnevskaya, V.S. 1991. Radiolarian layers of the<br />
USSR late Mesozoic. Izv. Akad. Nauk SSSR, ser. geol., 2,<br />
57-81. (in Russian)<br />
A <strong>radiolaria</strong>n biostratigralphy of Late Mesozoic units in the<br />
USSR is presented. It is based on three main regions: the Far East,<br />
the central regions and the south-vest of the USSR. Eleven typical<br />
<strong>radiolaria</strong>n layers are suggested for the Jurassic-Cretaceous<br />
volcanogenic-siliceous units in the Far Eastern region of the USSR.<br />
Thirteen <strong>radiolaria</strong>n layers are recognised in the siliceous-carbonate<br />
deposits of the Bol'shoy and Maly Kavkaz (Caucasus). These<br />
deposits are characterised by different kinds of fauna, namely<br />
ammonites, Inocerami and foraminifera. The <strong>radiolaria</strong>n layers may<br />
be used in ecological surveys.<br />
Vishnevskaya, V.S., Filatova, N.I. &<br />
Dvoryankin, A.I. 1991. New data on Jurassic sediments<br />
of Semiglavaya Mountain (Koryak Highland). Izv. Akad.<br />
Nauk SSSR, ser. geol., 4, 21-30. (in Russian)<br />
Detailed geological mapping was carried out in areas of the<br />
Koyverelan-Malyy Nauchirnynay interfluve and followed by<br />
laboratory analysis involving layer-by-layer sampling for <strong>radiolaria</strong>.<br />
This showed that the volcanogenic-siliceous-carbonate deposits in<br />
the region of Mount Semiglavaya, which form a series of tectonic<br />
plates pressed between Albian-Cenomanian terrigenous formations,<br />
include rocks not only of Upper Jurassic-Neocomian, but also of<br />
Middle Jurassic age. Analogous Middle Jurassic formations have also<br />
been discovered in the basins of the rivers Talyakaurkhyn and Malyy<br />
Nauchirnynay, where they occur as faulted tectonic plates or thin
Radiolaria 14 Bibliography - 1991<br />
scales. The Middle Jurassic <strong>radiolaria</strong>n complex is typical of<br />
relatively shallow-water conditions, while the Late Jurassic, typically<br />
Tethyan complex is characteristic of an open pelagic zone.<br />
Wang, Y.J. 1991. On progress in the study of Paleozoic<br />
<strong>radiolaria</strong>ns in China. Acta micropalaeont. sinica, 8/3, 237-<br />
251. (in Chinese)<br />
The study of Paleozoic <strong>radiolaria</strong>ns in China has been much<br />
improved ever since the publication of the first paper on Paleozoic<br />
Radiolaria in 1982(Sheng & Wang, 1982, in Chinese) with<br />
<strong>radiolaria</strong>n faunas ranging from Ordovician to Permian discovered in<br />
many localities. This paper gives a summary of the progress in the<br />
study of Paleozoic <strong>radiolaria</strong>ns during the last 10 years. All the<br />
materials used in this paper have not been published unless<br />
otherwise stated.<br />
Widz, D. 1991. Les Radiolaires du Jurassique supérieur des<br />
radiolarites de la zone des Klippes de Pieniny (Carpathes<br />
occidentales, Pologne). Rev. Micropaléont., 34/3, 231-260.<br />
About one hundred <strong>radiolaria</strong>n species have been found in forty<br />
three samples from radiolarites of the Pieniny Klippen Belt. For some<br />
species short descriptions or taxonomic remarks are given. The<br />
examination of the fauna allowed to identify the following Upper<br />
Jurassic Unitary Associations: U.A.7-8 (Oxfordian), U.A.8 (Upper<br />
Oxfordian) U.A.8-9 (Upper Oxfordian-Kimmeridgian). U.A.9<br />
(Kimmeridgian). In most cases these biostratigraphical results are in<br />
agreement with previous age-determination of these strata by<br />
aptychi.<br />
Yamashita, M., Ishida, K., Yamaoka, Y., Goto,<br />
H. & Ishiga, H. 1991. P/T boundary occurs in the "Toishi<br />
type" shale of southwest Japan. Appendix: Early Triassic<br />
<strong>radiolaria</strong>ns. Geol. Rep. Shimane Univ., 10, 47-52. (in<br />
Japanese)<br />
Yang, Q. 1991. Paleobiogeographic analysis of Jurassic<br />
Radiolaria. In: Palaeocology of China. (Jin, Y., Wang, J. &<br />
Xu, S., Eds.), vol. 1. pp. 233-248.<br />
Paleobiogeographic studies on Mesozoic Radiolaria are still in<br />
their infancy. Pessagno et al. distinguished the Tethyan and Boreal<br />
Faunal Realms which are further subdivided into four faunal<br />
provinces for Late Triassic and Jurassic Radiolaria. Their studies in<br />
North America together with Mizutani and Kojima's studies in East<br />
Asia on <strong>radiolaria</strong>n paleobiogeography have proved to be useful in<br />
tectonic investigations. The present study analyzes some of the<br />
important issues in <strong>radiolaria</strong>n paleobiogeographic studies and<br />
proposes an East Tethyan and a West Tethyan <strong>radiolaria</strong>n province<br />
for the Jurassic. The difference between the East Tethyan and West<br />
Tethyan <strong>radiolaria</strong>n assemblages is revealed by the fact that two<br />
different <strong>radiolaria</strong>n zonations of Pessagno et al. and Baumgartner<br />
for North America and the Mediterranean areas respectively are<br />
currently in parallel use. The East Tethyan province for Jurassic<br />
Radiolaria comprises Japan, China, Oman, Turkey, Greece, Italy,<br />
Switzerland and 'North Atlantic (DSDP sites), insofar as known, while<br />
the West Tethyan province includes east-central Mexico, California,<br />
Oregon, western Canada and probably Argentina. Such a faunal<br />
differentiation is a result of preliminary investigation and should be<br />
subjected to testing by more data from <strong>radiolaria</strong>n and other fossil<br />
groups and tectonic-paleooceanographic investigations.<br />
Abelmann, A. 1992a. Early to Middle Miocene <strong>radiolaria</strong>n<br />
stratigraphy of the Kerguelen Plateau, Leg 120. In:<br />
Proceedings of the Ocean Drilling Program, Scientific<br />
Results. (Wise, S.W.J., Schlich, R. et al., Eds.), vol. 120.<br />
College Station, TX (Ocean Drilling Program), pp. 757-783.<br />
Early to middle Miocene <strong>radiolaria</strong>n assemblages were examined<br />
at three sites (747, 748, and 751) that were cored during Ocean<br />
Drilling Program Leg 120 south of the present polar frontal zone on<br />
the Kerguelen Plateau (Indian sector of the Southern Ocean). The<br />
<strong>radiolaria</strong>n biostratigraphic study relies on a <strong>radiolaria</strong>n zonation<br />
recently developed on Leg 113 materials in the Atlantic sector of<br />
the Southern Ocean, which is correlated with the geomagnetic time<br />
scale. New <strong>radiolaria</strong>n biostratigraphic data also considering the<br />
established geomagnetic polarity record were used to improve and<br />
emend the age calibration of some lower Miocene <strong>radiolaria</strong>n zones<br />
and a redefined middle Miocene <strong>radiolaria</strong>n zonation is proposed.<br />
Based on these results, a revised age assignment of the lower<br />
Miocene sections drilled at Leg 113 Sites 689 and 690 is proposed.<br />
1992<br />
- 73 -<br />
Yang, Q. & Mizutani, S. 1991. Radiolaria from the<br />
Nadanhada Terrane, Northeast China. J. Earth Sci. Nagoya<br />
Univ., 38, 49-78.<br />
The Nadanhada Terrane located in the northeastern part of<br />
Heilongjiang Province, northeast China, is correlative to the Mino<br />
Terrane of Japan. The geologic and biostratigraphic studies have<br />
been done particularly in terms of terrane analysis, and the<br />
Mesozoic tectonics of the western Pacific has been discussed on the<br />
basis of these study results. This paper outlines the geology and<br />
biostratigraphy of the Nadanhada Terrane and presents new data of<br />
<strong>radiolaria</strong>n micropaleontology. Abundant and diversified<br />
parasaturnalids associated with other groups of Radiolaria were<br />
discovered from Upper Triassic and Lower Jurassic strata of the<br />
Nadanhada Terrane. Fourteen species-level taxa under six genera of<br />
the Parasaturnalidae are illustrated in this paper, including five new<br />
species (Praemesosaturnalis heilongjiangensis, Pseudoheliodiscus<br />
rotundus, Saturnosphaera shengi, Saturnosphaera zhangi, and<br />
Stauracanthocircus nadanhadaensis).<br />
The parasaturnalids from the Triassic-Jurassic transitional<br />
strata in the Nadanhada Terrane show significant morphological<br />
changes from latest Triassic to earliest Jurassic times. Notably Late<br />
Triassic parasaturnalids have a broader peripheral ring and mostly<br />
possess auxiliary rays or more than two undifferentiated rays; on<br />
the other hand, in the lowermost Jurassic occurs abundant<br />
Palaeosaturnalis Donofrio and Mostler sensu Kozur and Mostler;<br />
some species of Palaeosaturnalis are distinctive for lowermost<br />
Jurassic, such as P. Iiassicus Kozur and Mostler, P. Ienggriesensis K.<br />
& M. and their related forms; the earliest Jurassic parasaturnalids<br />
commonly possess a narrow peripheral ring, and species with<br />
auxiliary rays or more than two undifferentiated rays are less<br />
abundant. This study indicates that the parasaturnalids, together<br />
with other <strong>radiolaria</strong>n groups, may be used as good markers for<br />
identifying Upper Triassic and Lower Jurassic strata and have a<br />
great potential for determining the T/J boundary.<br />
Based on the new data and on a selected set of morphological<br />
criteria, one of the authors (Q. Yang) intends to propose a revised<br />
classification of the Mesozoic ring-type Radiolaria in order to<br />
simplify the taxonomy. Revised parasaturnalid genera now include<br />
Acanthocircus (incl. synonyms Eospongosaturnalis, Hexasaturnalis,<br />
Spongosaturnalis and Spongosaturninus), Heliosaturnalis,<br />
Mesosaturnalis (incl. Pseudacanthocircus), Palaeosaturnalis (incl.<br />
Praehexasaturnalis and Spinoellipsella), Praemesosaturnalis,<br />
Pseudoheliodiscus (incl. Liassosaturnalis, Octosaturnalis and<br />
Pessagnosaturnalis), Saturnosphaera (incl. Praeacanthocircus,<br />
Stauromesosaturnalis and Triacanthocircus), Stauracanthocircus,<br />
Yaosaturnalis (incl. Kozurastrum), and multiple-ringed genera such<br />
as Japonisaturnalis, Parasaturnalis and Pseudosaturnalis.<br />
Yao, A. 1991a. Prospects in biochronology: A comment<br />
from the viewpoint of Mesozoic <strong>radiolaria</strong>n chronology. In:<br />
Problems and prospects of paleontology in 21st century;<br />
reports on 1991 annual meeting of the Paleontological<br />
Society of Japan. Eds.), vol. 50. Fossils, pp. 8-9. (in<br />
Japanese)<br />
Yao, A. 1991b. Occurrence of Paleozoic <strong>radiolaria</strong>ns from<br />
eastern inner Mongolia. In: Pre-Jurassic Geology of Inner<br />
Mongolia, China. (Ishii, K., Liu, X., Ichikawa, K. & Huang,<br />
B., Eds.). Report of China-Japan Cooperative Research<br />
Group, pp. 175-187.<br />
Abelmann, A. 1992b. Radiolarian flux in the Antarctic<br />
waters (Drake Passage, Powell Basin, Bransfield Strait). Polar<br />
Biol., 12, 357-372.<br />
The study of <strong>radiolaria</strong>ns collected during sediment trap<br />
experiments in the Drake Passage, the northern Powell Basin, and the<br />
King George Basin of the Bransfield Strait provides new information<br />
on the flux rates of <strong>radiolaria</strong>n shells in Antarctic waters, on the<br />
annual flux pattern, the species distribution and its ecological<br />
significance, and on alteration processes of the <strong>radiolaria</strong>n shells in<br />
the water column and at the sediment/water interface. A 28-month<br />
monitoring with time-series sediment traps in the Bransfield Strait<br />
indicates an annual flux pattern characterized by short-term flux<br />
pulses during austral summer, which reach daily flux rates of up to 5<br />
x 10 3 shells m -2 and account for more than 90 % of the total annual<br />
flux. The distinct seasonal variations are linked to variations In the<br />
sea Ice coverage. Other controlling factors are the production of<br />
phytoplankton and the Impact by zooplankton grazers, e. g. the krill.<br />
The vertical flux rates of <strong>radiolaria</strong>ns of the summer flux pulses
Bibliography - 1992 Radiolaria 14<br />
range between ca. 3 and 21 x 10 4 shells m -2 , values that are at one<br />
or more magnitudes lower than flux rates observed at sites in the<br />
tropical and northern high-latitude ocean. Significant lateral<br />
transport of <strong>radiolaria</strong>ns was documented during austral summer in<br />
the Bransfleld Strait by a factor of 10 Increase of the <strong>radiolaria</strong>n<br />
flux in the lower portion of the water column and the species<br />
composition trapped in deeper waters.<br />
Radiolarian assemblages associated with pelagic and neritic<br />
environments characterized by typical Antarctic taxa (Antarctissa<br />
spp.) and a group of species with bipolar distribution (e. g.<br />
Plectacantha oikiskos, Phormacantha hystrix), respectively, are<br />
distinguished. While the signal of polycystine <strong>radiolaria</strong>ns is<br />
relatively well recorded in the sediments, the shells of phaeodarians,<br />
which were observed at flux rates of up to 1x10 3 shells m -2 day -1 in<br />
the upper portion of the water column, are almost completely<br />
dlssolved during settling in the water column.<br />
Abelmann, A. 1992c. Radiolarian taxa from Southern<br />
Ocean sediment traps (Atlantic sector). Polar Biol., 12, 373-<br />
385.<br />
This study gives a first inventory of <strong>radiolaria</strong>n taxa collected<br />
with sediment traps in different areas of the Southern Ocean (Drake<br />
Passage, Powell Basin and Bransfield Strait). It includes 66 taxa or<br />
taxa groups of which 46 were already described. Two previously<br />
described species groups and 20, yet undescribed, taxa are<br />
documented. The name Protocystis bicornis (Haecker) is replaced by<br />
P. spinosus as it is a later homonym of P. bicornis (Borgert). The<br />
occurrence pattern of the <strong>radiolaria</strong>n taxa indicates distinct<br />
differences in the species composition between neritic environments<br />
(Bransfield Strait and Powell Basin) and pelagic, open ocean<br />
conditions (Drake Passage).<br />
Adachi, M., Kojima, S., Wakita, K., Suzuki, K.<br />
& Tanaka, T. 1992. Transect of Central Japan: from Hida<br />
to Shimanto. In: Paleozoic and Mesozoic Terranes: Basement<br />
of the Japanese Island Arcs. 29th IGC Field Trip Guide Book.<br />
(Adachi, M. & Suzuki, K., Eds.), vol. 1. Nagoya University,<br />
Nagoya, Japan. pp. 143-178.<br />
Afanasieva, M.S. & Vishnevskaya, V.S. 1992. A<br />
possible cause of the generation of the silica skeleton in<br />
Radiolaria. Dokl. Akad. Nauk SSSR, 325/3, 590-596. (in<br />
Russian)<br />
Aguado, R., Company, M., O'Dogherty, L.,<br />
Sandoval, J. & Tavera, J.M. 1992. Biostratigraphic<br />
analysis of the pelagic Barremian/Aptian in the Betic<br />
Cordillera (southern Spain): preliminary data. Cretaceous<br />
Res., 13/5-6, 445-452.<br />
The Lower Cretaceous rhythmic sequences (marls and marly<br />
limestones) of the pelagic domain in the Betic Cordillera (Subbetic<br />
Zone) provide optimal conditions for integrated biostratigraphic<br />
scales based on different fossil groups. In this paper we present a<br />
preliminary study of the stratigraphic distribution of different<br />
species of ammonites, planktonic foraminifera, calcareous<br />
nannofossils and <strong>radiolaria</strong> recorded principally in one Barremian-<br />
Aptian section in Jaen (Andalusia, southern Spain).<br />
For the ammonites, which are present only in the Barremian and<br />
probably in the lowermost Aptian, it appears reasonable to use the<br />
zonation proposed by Busnardo (1984) for SE France. Planktonic<br />
foraminifera can be differentiated in seven zones (Hedbergella<br />
sigali, Globigerinelloides blowi, Hedbergella trocoidea, Leupoldina<br />
cabri, Globigerinelloides algerianus, Planomalina cheniourensis and<br />
Ticinella bejaouaensis) for the Barremian-Aptian interval. Four<br />
interval zones (Lithraphidites bollii, Micrantholithus hoschulzii,<br />
Hayesites irregularis and Rhagodiscus angustus) can be<br />
distinguished according to the vertical distribution of the calcareous<br />
nannofossil species. Finally, two <strong>radiolaria</strong>n assemblages can be<br />
identified, a lower one for the Barremian-Lower Aptian and an upper<br />
one for the Upper Aptian. Correlations between the scales used in<br />
this paper are established.<br />
Aita, Y. & Grant-Mackie, J.A. 1992. Late Jurassic<br />
Radiolaria from the Kowhai Point siltstone, Murihiku terrane,<br />
North Island, New Zealand. In: Centenary of Japanese<br />
Micropaleontology. (Ishizaki, K. & Saito, T., Eds.). Terra<br />
Scientific Publishing Company, Tokyo, Japan. pp. 375-382.<br />
Detailed evidence of Late Jurassic Radiolaria is presented from<br />
the Kowhai Point Siltstone in the Murihiku terrane, North Island, New<br />
Zealand. Nineteen <strong>radiolaria</strong>n species including Acaeniotyle<br />
diaphorogona, Pantanellium riedeli, Pseudocrucella cf. sanfilippoae,<br />
Hsuum maxwelli, etc. are identified in an ammonite-bearing<br />
- 74 -<br />
calcareous concretion. The estimated age of this fauna is<br />
Kimmeridgian based upon recent studies of dinoflagellates and<br />
molluscs (Davey, 1987; Helby et al, 1988). The Murihiku fauna is<br />
similar in composition to coeval faunas from Tethyan, Japanese and<br />
North American sequences and shows a strong cosmopolitan<br />
affinity. A comparison of the Murihiku <strong>radiolaria</strong>ns with the coeval<br />
Waipapa terrane fauna of an origin in the Southern Hemisphere high<br />
latitudes (Spörli and Aita, 1988) gives significant evidence in<br />
clarifying the paleobiogeography of Mesozoic Radiolaria.<br />
Aita, Y. & Spörli, K.B. 1992. Tectonic and<br />
paleobiogeographic significance of <strong>radiolaria</strong>n microfaunas<br />
in the Permian to Mesozoic basement rocks of the North<br />
Island, New Zealand. In: Significance and application of<br />
Radiolaria to terrane analysis. (Aitchison, J.C. & Murchey,<br />
B.L., Eds.), vol. 96/1-2. Special Issue: Palaeogeogr.<br />
Palaeoclimatol. Palaeoecol., Elsevier, Amsterdam. pp. 103-<br />
125.<br />
From the terranes sutured to the New Zealand Gondwana margin<br />
in mid-Cretaceous time, the Murihiku, Waipapa, Torlesse and Mata<br />
River terranes have yielded tectonically and paleogeographically<br />
significant <strong>radiolaria</strong>n faunas. A late Jurassic fauna from the<br />
Murihiku forearc terrane is more cosmopolitan than coeval faunas<br />
from the Waipapa.<br />
Faunas from the terranes east of the Murihiku, which all show<br />
evidence of accretion tectonics, can be subdivided into ocean floor<br />
assemblages and assemblages of terrigenous clastic deposits.<br />
Waipapa ocean floor assemblages are typically Tethyan while the<br />
terrigenous clastic assemblages are non-Tethyan, possibly of<br />
southern hemisphere high latitude origin. Ocean floor assemblages<br />
show the same eastward younging trends, opposed to the westward<br />
sedimentological younging, due to imbrication, as do the<br />
assemblages of the terrigenous clastics, but are always a few tens<br />
of million years older.<br />
Radiolarians from ophiolites (Tangihua Volcanics and Matakaoa<br />
Volcanics) indicate that significant portions of the ocean floor<br />
obducted onto New Zealand in late Oligocene to earliest Miocene<br />
time were of Late Cretaceous to Early Tertiary age.<br />
Aitchison, J.C. 1992. Radiolarians from sediments of the<br />
Izu-Bonin region, Leg 126. In: Proceedings of the Ocean<br />
Drilling Program, Scientific Results. (Taylor, B., Fujioka, K.<br />
et al., Eds.), vol. 126. College Station, TX (Ocean Drilling<br />
Program), pp. 321-330.<br />
Radiolarians occur at five Leg 126 sites. Well-preserved<br />
<strong>radiolaria</strong>ns were recovered from Miocene and Pliocene through<br />
Holocene sections. The results of this study may help to fill the<br />
informational gap on Quaternary <strong>radiolaria</strong>n distribution at midlatitudes<br />
in the western Pacific. Radiolarian preservation is<br />
discontinuous, and, although present in Oligocene sections,<br />
specimens are poorly preserved.<br />
Aitchison, J.C. & Flood, P.G. 1992. Implications of<br />
<strong>radiolaria</strong>n research for analysis of subduction complex<br />
terranes in the New England Orogen, NSW, Australia. In:<br />
Significance and application of Radiolaria to terrane<br />
analysis. (Aitchison, J.C. & Murchey, B.L., Eds.), vol.<br />
96/1-2. Special Issue: Palaeogeogr. Palaeoclimatol.<br />
Palaeoecol., Elsevier, Amsterdam. pp. 89-102.<br />
Radiolarians provide important age constraints on geologically<br />
complex strata in the New England Orogen of eastern Australia.<br />
Several terranes interpreted as subduction complexes were undated<br />
prior to <strong>radiolaria</strong>n studies. Radiolarian faunas indicate that the<br />
Djungati terrane is significantly younger than the previously inferred<br />
Ordovician to Silurian age range. Basalt-chert successions in the<br />
Djungati terrane developed during the Silurian to Late Devonian in an<br />
environment which was far from the influence of terrigenous<br />
sedimentation. Radiolarians from tuffs within overlying arc-derived<br />
volcaniclastic sequences constrain the timing of tectonic assembly<br />
of the terrane at a convergent margin to the latest Devonian-Early<br />
Carboniferous. The extensive, but previously undated, Anaiwan<br />
terrane also contains <strong>radiolaria</strong>ns which indicate a latest Devonian<br />
to Early Carboniferous age for siliceous oceanic sediments. These<br />
sediments were accreted into a subduction complex. Volcaniclastic<br />
sediments within this subduction complex contain <strong>radiolaria</strong>ns which<br />
indicate that it developed during the Early Carboniferous.<br />
Radiolarians in the Willowie Creek beds provide the first age<br />
constraints (Late Devonian) for another lithotectonic entity, the<br />
Yugambal terrane, which is located along the eastern edge of the<br />
southern New England orogen. Many of the recently determined<br />
<strong>radiolaria</strong>n ages are at variance with age estimates used to develop<br />
models for the tectonic development of the orogen. These new age<br />
data require major reappraisal of models. Detailed analysis of the
Radiolaria 14 Bibliography - 1992<br />
geological evolution of individual terranes is required before an<br />
integrated model for the entire orogen can be developed.<br />
Aitchison, J.C., Flood, P.G. & Spiller, F.C.O.<br />
1992. Tectonic setting and paleoenvironment of terranes in<br />
the southern New England Orogen, eastern Australia as<br />
constrained by <strong>radiolaria</strong>n biostratigraphy. Palaeogeogr.<br />
Palaeoclimatol. Palaeoecol., 94/1-4, 31-54.<br />
Radiolarians are abundant in the Gamilaroi, Djungati and<br />
Anaiwan terranes of the New England orogen in eastern Australia.<br />
These microfossils present the first age constraints on the timing of<br />
development of hitherto undated lithologies within the various<br />
juxtaposed terranes of the orogen. They give a biostratigraphic<br />
framework for interpreting the history of marine sedimentation in<br />
these terranes and have significant implications for published<br />
tectonic models<br />
Radiolarians also show that the stratigraphically lowermost<br />
rocks or the Gamilaroi terrane are most probably of' Devonian age.<br />
Better stratigraphic resolution permits interpretation of these rocks<br />
as part of an intra-oceanic island arc succession which accreted to<br />
the eastern margin of Australia (Gondwana) around the end of the<br />
Devonian. This intra-oceanic arc is distinct from a younger,<br />
Carboniferous, superposed continental arc sequence which<br />
constitutes a successor basin that developed over the Gamilaroi<br />
terrane subsequent to its accretion to the margin of Australia.<br />
Radiolarians provide the basis for dating siliceous lithologies<br />
which dominate the Djungati terrane and permit a more detailed<br />
analysis of the history of this terrane. During the middle Silurian<br />
through Late Devonian the Djungati terrane was part of an oceanic<br />
basin which was isolated from any source of terrigenous<br />
sedimentation. The Djungati terrane was subsequently influenced by<br />
volcanic island arc activity and was tectonically disrupted during the<br />
latest Devonian to Early Carboniferous. Radiolarian age data show<br />
that age correlations inferred, on the basis of similarities in detrital<br />
sandstone petrography, between lithostratigraphic units in the<br />
Gamilaroi and Djungati terranes, are not always appropriate. Djungati<br />
terrane has been widely interpreted as a subduction complex related<br />
to the Gamilaroi terrane. Radiolarian data now elucidate much of the<br />
structural complexity of this terrane. Significant differences<br />
between the Djungati terrane and the style of well-documented<br />
subduction complexes include the close spacing of zones of<br />
<strong>radiolaria</strong>n chert, the dominance of this lithology over others and the<br />
lateral extent of many of the chert horizons.<br />
The Anaiwan terrane has features which are characteristic of<br />
many well-documented subduction complexes. Radiolarians are<br />
abundant in this terrane and can be used to show that it developed<br />
along the eastern margin of Australia in response to Early<br />
Carboniferous subduction of Late Devonian to Early Carboniferous<br />
oceanic crust. Packages of chert accreted into the subduction<br />
complex are progressively younger towards the northeast indicating<br />
that subduction was directed to the southwest.<br />
Aitchison, J.C. & Murchey, B.L. (Eds) 1992. The<br />
significance and application of Radiolaria to Terrane<br />
Analysis. Special issue of Palaeogeography,<br />
Palaeoclimatology, Palaeoecology, Elsevier Amsterdam.<br />
96, 172 p.<br />
Alexandrovich, J.M. 1992. Radiolarians from Sites 794,<br />
795, 796, and 797 (Japan Sea). In: Proceedings of the Ocean<br />
Drilling Program, Scientific Results. (Tamaki, K., Ingle,<br />
J.C.J. et al., Eds.), vol. 127-128/1. College Station, TX<br />
(Ocean Drilling Program), pp. 291-307.<br />
Japan Sea ODP Leg 127 shipboard <strong>radiolaria</strong>n biostratigraphic<br />
data are compiled and improved. The sequence of biostratigraphic<br />
events determined in sediments above the opal-A/opal-CT transition<br />
is illustrated graphically with depth-depth plots. The absence of<br />
biostratigraphic indicators from the North and subtropical Pacific<br />
and differences between the compositions of the Japan Sea and<br />
Pacific <strong>radiolaria</strong>n assemblages suggest that the planktonic<br />
populations of the Japan Sea have been partially isolated from the<br />
Pacific since the late Miocene. Subtropical fauna in sediments<br />
younger than ~1.8 Ma at Site 797 record the occurrence of a paleo-<br />
Tsushima current. These same fauna record larger volumes of the<br />
paleo-Tsushima current, or warmer intervals during the colder glacial<br />
climate regime at Site 794. The variability of Pleistocene<br />
assemblage composition and preservation shows that <strong>radiolaria</strong>n<br />
dissolution has played a large part in determining what is preserved.<br />
Preliminary taxonomic evaluations are made, and the stratigraphic<br />
and paleoceanographic implications of <strong>radiolaria</strong>n species are<br />
discussed.<br />
Amon, E.O. 1992. Some materials to the revision of<br />
Prunobrachium genus (Radiolaria, Sphaerellaria). In:<br />
- 75 -<br />
Materials on Paleontology and Stratigraphy of the Western<br />
Siberia. (Podobina, V.M., Eds.). Tomsk Univ. Publisher,<br />
Tomsk. pp. 84-87. (in Russian)<br />
Amon, E.O. & Chuvasov, B.I. 1992. Early Permian<br />
<strong>radiolaria</strong>n associations of the type section "Sim" of the<br />
Southern Urals. In: New data on Paleozoic stratigraphy and<br />
lithology of Urals and Middle Asia. Nauka Publisher,<br />
Ekaterinburg. pp. 96-108. (in Russian)<br />
Amon, E.O. & Korovko, A.V. 1992. First data about<br />
late Devonian <strong>radiolaria</strong>n association from Rezhevskaya<br />
structural-facial zone of Eastern Middle Urals. In: New data on<br />
Paleozoic stratigraphy and lithology of Urals and Middle<br />
Asia. Nauka Publisher, Ekaterinburg. pp. 69-77. (in Russian)<br />
Anderson, O.R. & Matsuoka, A. 1992.<br />
Endocytoplasmatic microalgae and bacteroids within the<br />
central capsule of the <strong>radiolaria</strong>n. Symbiosis, 12, 237-247.<br />
Micro-algae (c. 2.5 to 3.5 µm wide x3.8 to 4.5 µm long) occur<br />
abundantly within perialgal vacuoles in the intracapsular cytoplasm<br />
of the <strong>radiolaria</strong>n Dyctyocoryne truncatum, a triangular-shaped,<br />
spongiose skeletal <strong>radiolaria</strong>n. The fine structure of the microalgae<br />
resembles that of yellow-brown pigmented symbionts observed in<br />
larger spongiose skeletal <strong>radiolaria</strong> of the spongodrymid type. The<br />
density of microalgae in a typical ultrathin section is c. 4/100 µm 2 .<br />
Bacteroids (0.2x0.5 µm) are present throughout the intracapsular<br />
cytoplasm. There is no evidence of a vacuolar membrane enclosing<br />
the bacteroids, but each is surrounded by an electron lucent zone.<br />
The central capsule of <strong>radiolaria</strong> contains the nucleus and<br />
cytoplasmic organelles and is bounded by a capsular wall. Previously,<br />
algae associated with <strong>radiolaria</strong> have been observed in the<br />
extracapsulum. The occurrence of intracapsular microalgae in D.<br />
truncatum is of interest since this indicates that the intracapsular<br />
cytoplasm, previously thought to be largely specialized for<br />
metabolism, storage of reserve substances and production of<br />
reproductive swarmers, can also be a site for host-algal<br />
interactions.<br />
Baumgartner, P.O. 1992. Lower Cretaceous <strong>radiolaria</strong>n<br />
biostratigraphy and biogeography off northwestern<br />
Australian (ODP sites 765 and 766 and DSDP site 261), Argo<br />
abyssal plain and lower Exmouth Plateau. In: Proceedings of<br />
the Ocean Drilling Program, Scientific Results. (Gradstein,<br />
F.M., Ludden, J.N. et al., Eds.), vol. 123. College Station,<br />
TX (Ocean Drilling Program), pp. 299-342.<br />
During Leg 123, abundant and well-preserved Neocomian<br />
<strong>radiolaria</strong>ns were recovered at Site 765 (Argo Abyssal Plain) and<br />
Site 766 (lower Exmouth Plateau). The assemblages are<br />
characterized by a scarcity or absence of Tethyan taxa. The<br />
Berriasian-early Aptian <strong>radiolaria</strong>n record recovered at Site 765 is<br />
unique in its density of well-preserved samples and in its faunal<br />
contents. Remarkable contrasts exist between <strong>radiolaria</strong>n<br />
assemblages extracted from claystones of Site 765 and reexamined<br />
DSDP Site 261, and faunas recovered from <strong>radiolaria</strong>n sand layers of<br />
Site 765. Clay faunas are unusual in their low diversity of apparently<br />
ecologically tolerant species, whereas sand faunas are dominated by<br />
non-Tethyan species that have never been reported before.<br />
Comparisons with Sites 766 and 261, as well as sedimentological<br />
observations, lead to the conclusion that this faunal contrast results<br />
from a difference in provenance, rather than from hydraulic sorting.<br />
Biostratigraphic dating proved difficult principally because of<br />
the paucity or even absence of (Tethyan) species used in published<br />
zonations. In addition, published zonations are contradictory and do<br />
not reflect total ranges of species.<br />
Radiolarian assemblages recovered from claystones at Sites<br />
765 and 261 in the Argo Basin reflect restricted oceanic conditions<br />
for the latest Jurassic to Barremian time period. Neither the<br />
sedimentary facies nor the faunal associations bear any<br />
resemblance to sediment and <strong>radiolaria</strong>n facies observed in typical<br />
Tethyan sequences. I conclude that the Argo Basin was<br />
paleoceanographically separated from Tethys during the Late<br />
Jurassic and part of the Early Cretaceous by its position at a higher<br />
paleolatitude and by enclosing landmasses, i.e., northeastern India<br />
and the Shillong Block, which were adjacent to the northwestern<br />
Australian margin before the opening.<br />
Assemblages recovered from <strong>radiolaria</strong>n sand layers are<br />
dominated by non-Tethyan species that are interpreted as<br />
circumantarctic. Their sudden appearance in the late<br />
Berriasian/early Valanginian pre-dates the oceanization of the Indo-<br />
Australian break-up (M11, late Valanginian) by about 5 m.y., but<br />
coincides with a sharp increase in margin-derived pelagic turbidites.<br />
The Indo-Australian rift zone and its adjacent margins probably were
Bibliography - 1992 Radiolaria 14<br />
submerged deeply enough to allow an intermittent "spillover" of<br />
circumantarctic cold water into the Argo Basin, creating increased<br />
bottom current activity. Circumantarctic cold-water <strong>radiolaria</strong>ns<br />
transported into the Argo Basin upwelled along the margin and died<br />
en masse. Concomitant winnowing by bottom currents led to their<br />
accumulation in distinct radiolarite layers. High rates of faunal<br />
change and the sharp increase of bottom current activity are<br />
thought to be synchronous with the two pronounced late Berriasianearly<br />
Valanginian lowstands in sea level. Hypothetically, both<br />
phenomena might have been caused by a glaciation on the Antarctic-<br />
Australian continent, which was for the first time isolated from the<br />
rest of Gondwana by oceanic seaways as a result of Jurassic and<br />
Early Cretaceous seafloor spreading.<br />
The absence of typical Tethyan <strong>radiolaria</strong>n species during the<br />
late Valanginian to late Hauterivian period is interpreted as<br />
reflecting a time of strong influx of circumantarctic cold water<br />
following oceanization (M11) and rapid spreading between southeast<br />
India and western Australia.<br />
The reappearance and gradual increase in abundance and<br />
diversity of Tethyan forms along with the still dominant<br />
circumantarctic species are thought to result from overall more<br />
equitable climatic conditions during the Barremian and early Aptian<br />
and may have resulted from the establishment of an oceanic<br />
connection with the Tethys Ocean during the early Aptian.<br />
Baumgartner, P.O., Bown, P., Marcoux, J.,<br />
Mutterlose, J., Kaminski, M., Haig, D. &<br />
McMinn, A. 1992. Early Cretaceous biogeographic and<br />
oceanographic synthesis of Leg 123 (off northern Australia).<br />
In: Proceedings of the Ocean Drilling Program, Scientific<br />
Results. (Gradstein, F.M., Ludden, J.N. et al., Eds.), vol.<br />
126. College Station, TX (Ocean Drilling Program), pp.<br />
739-758.<br />
Biogeographic observations made by Leg 123 shipboard<br />
paleontologists for Lower Cretaceous nannofossils, foraminifers,<br />
<strong>radiolaria</strong>ns, belemnites, and inoceramids are combined in this<br />
chapter to evaluate the paleoceanographic history of the<br />
northwestern Australian margin and adjacent basins. Each fossil<br />
group is characterized at specific intervals of Cretaceous time and<br />
compared with data from Tethyan and Southern Hemisphere highlatitude<br />
localities. Special attention is given to the biogeographic<br />
observations made for the Falkland Plateau (DSDP Legs 36 and 71)<br />
and the Weddell Sea (ODP Leg 113). Both areas have yielded<br />
valuable Lower Cretaceous fossil records of the circumantarctic<br />
high latitudes.<br />
In general, the Neocomian fossil record from DSDP and ODP<br />
sites off northwestern Australia has important southern highlatitude<br />
affinities and weak Tethyan influence. The same is true for<br />
the pelagic lithofacies: <strong>radiolaria</strong>n chert and/or nannofossil<br />
limestone, dominant in the Tethyan Lower Cretaceous, are minor<br />
lithologies in the Exmouth-Argo sites. These observations, together<br />
with the young age of the Argo crust and plate tectonic<br />
considerations, suggest that the Argo Basin was not part of the<br />
Tethys Realm.<br />
The biogeography of the Neocomian <strong>radiolaria</strong>n and nannofossil<br />
assemblages suggests opening of a seaway during the Berriasian<br />
that connected the circumantarctic area with the Argo Basin, which<br />
resulted in the influx of southern high-latitude waters.<br />
This conclusion constrains the initial fit and break-up history of<br />
Gondwana. Our results favor the loose fit of the western Australian<br />
margin with southeast India by Ricou et al. (1990), which accounts<br />
for a deeper water connection with the Weddell-Mozambique basins<br />
via drowned marginal plateaus as early as the Berriasian. In fits of<br />
the du Toit-type (1937), India would remain attached to Antarctica,<br />
at least until the late Valanginian, making such a connection<br />
impossible.<br />
After the Barremian, increasing Tethyan influence is evident in<br />
all fossil groups, although southern high-latitude taxa are still<br />
present. Biogeographic domains, such as the southern extension of<br />
Nannoconus and Ticinella suggest paleolatitudes of about 50°S for<br />
the Exmouth-Argo area. Alternatively, if paleolatitudes of about 35°<br />
are accepted, these biogeographic limits were displaced northward<br />
at least 15° along Australia in comparison to the southern Atlantic.<br />
In this case, the proto-circumantarctic current was deflected<br />
northward into an eastern boundary current off Australia and carried<br />
circumantarctic cold water into the middle latitudes.<br />
Late Aptian/early Albian time is characterized by mixing of<br />
Tethyan and southern faunal elements and a significant gradient in<br />
Albian surface-water temperatures over 10° latitude along the<br />
Australian margin, as indicated by planktonic foraminifers. Both<br />
phenomena may be indicative of convergence of temperate and<br />
antarctic waters near the Australian margin. High fertility<br />
conditions, reflected by <strong>radiolaria</strong>n cherts, are suggestive of coastal<br />
upwelling during that time.<br />
- 76 -<br />
Behl, R.J. & Smith, B.M. 1992. Silicification of deepsea<br />
sediments and the oxygen isotope composition of<br />
diagenetic siliceous rocks from the western Pacific, Pigafetta<br />
and east Mariana Basin, Leg 129. In: Proceedings of the<br />
Ocean Drilling Program, Scientific Results. (Larsen, R.L.,<br />
Lancelot, Y. et al., Eds.), vol. 129. College Station, TX<br />
(Ocean Drilling Program), pp. 81-117.<br />
Ocean Drilling Program Leg 129 recovered chert, porcellanite,<br />
and radiolarite from Middle Jurassic to lower Miocene strata from<br />
the western Pacific that formed by different processes and within<br />
distinct host rock. These cherts and porcellanite formed by (l)<br />
replacement of chalk or limestone, (2) silicification and in-situ silica<br />
phase-transformation of bedded clay-bearing biosiliceous deposits,<br />
(3) high-temperature silicification adjacent to volcanic flows or sills,<br />
and (4) silica phase-transformation of mixed biosiliceousvolcaniclastic<br />
sediments.<br />
Petrologic and O-isotopic studies highlight the key importance<br />
of permeability and time in controlling the formation of dense cherts<br />
and porcellanites. The formation of dense, vitreous cherts<br />
apparently requires the local addition and concentration of silica.<br />
The influence of permeability is shown by two examples, in which: (1)<br />
fragments of originally identical radiolarite that were differentially<br />
isolated from pore-water circulation by cement-filled fractures were<br />
silicified to different degrees, and (2) by the development of<br />
secondary porosity during the opal-CT to quartz inversion within<br />
conditions of negligible permeability. The importance of time is<br />
shown by the presence of quartz chert below, but not above, a<br />
Paleogene hiatus at Site 802, indicating that between 30 and 52<br />
m.y. was required for the formation of quartz chert within<br />
calcareous-siliceous sediments.<br />
The oxygen-isotopic composition for all Leg 129 carbonateand<br />
Fe/Mn-oxide-free whole-rock samples of chert and porcellanite<br />
range widely from ∂1 8 O = 27.8 ‰ to 39.8 ‰ vs. V-SMOW. Opal-CT<br />
samples are consistently richer in 18 O (34.1 ‰ to 39.3 ‰ ) than<br />
quartz subsamples (27.8 ‰ to 35.7 ‰ ). Using the O-isotopic<br />
fractionation expression for quartz-water of Knauth and Epstein<br />
(1976) and assuming ∂ 18 Opore water =-1.0 ‰, model temperatures<br />
of formation are 7°-26°C for carbonate-replacement quartz .cherts,<br />
22°-25°C for bedded quartz cherts, and 32°-34°C for thermal quartz<br />
cherts. Large variations in O-isotopic composition exist at the same<br />
burial depth between co-existing silica phases in the same sample<br />
and within the same phase in adjacent lithologies. For example.<br />
quartz has a wide range of isotopic compositions within a single<br />
breccia sample: ∂ 18 O = 33.4 ‰ and 28.0 ‰ for early and late<br />
stages of fracture-filling cementation, and 31.6 ‰ and 30.2 ‰ for<br />
microcrystalline quartz precipitation within enclosed chert and<br />
radiolarite fragments. Similarly, opal-CT d101 spacing varies across<br />
lithologic or diagenetic boundaries within single samples.<br />
Co-occurring opal-CT and chalcedonie quartz in shallowly buried<br />
chert and porcellanite from Sites 800 and 801 have an 8.7 ‰<br />
difference in ∂ 18 O, suggesting that pore waters in the Pigafetta<br />
Basin underwent a Tertiary shift to strongly l8 O-depleted values due<br />
to alteration of underlying Aptian to Albian-Cenomanian<br />
volcaniclastic deposits after opal-CT precipitation, but prior to<br />
precipitation of microfossil-filling chalcedony.<br />
Bernstein, R.E., Byrne, R., Betzer, P.R. &<br />
Greco, A.M. 1992. Morphologies and transformations of<br />
celestite in seawater: the role of acantharians in strontium and<br />
barium geochemistry. In: The Robert M. Garrels Memorial<br />
Issue. (Helgeson, H.C., Eds.), vol. 56/8. Geochimica et<br />
cosmochimica Acta, pp. 3273-3279.<br />
Free-drifting sediment traps deployed at 400, 1500, and 3200<br />
m were used to collect particles near the USJGOFS Time-Series<br />
Station (31°49.5'N and 64°08.2'W) in the Atlantic Ocean.<br />
Acantharian specimens isolated from our samples were abundant at<br />
the 400-m depth horizon and were rare to non-existent in our 1500m<br />
traps. No specimens were detected in the 3200-m traps. This<br />
trend parallels those noted for the Pacific and has been linked to the<br />
oceans' Sr/CI profiles. Our collections revealed the presence of<br />
myriad, heretofore undocumented, minute SrSO4 particles. These<br />
particles are most likely related to the acantharian reproductive<br />
cycle. The extreme abundance of acantharians and acantharianderived<br />
particles may have implications beyond the oceans' Sr<br />
budgets. Barium/strontium molar ratios in acantharian-derived<br />
celestite on the order of 3 X 10 -3 indicate that acantharians may<br />
play an important role in oceanic Ba cycling.<br />
Blome, C.D. 1992. Radiolarians from Leg 122, Exmouth<br />
and Wombat Plateaus, Indian Ocean. In: Proceedings of the<br />
Ocean Drilling Program, Scientific Results. (Von Rad, U.,<br />
Haq, B.U. et al., Eds.), vol. 122. College Station, TX (Ocean<br />
Drilling Program), pp. 633-652.
Radiolaria 14 Bibliography - 1992<br />
Sites 759 through 764 were drilled during Ocean Drilling<br />
Program Leg 122 on the Exmouth and Wombat plateaus off<br />
northwest Australia, eastern Indian Ocean. Radiolarian recovery was<br />
generally poor due to unsuitable lithofacies. A few Quaternary<br />
<strong>radiolaria</strong>n faunas were recovered from most of the sites. Rare and<br />
poorly preserved Oligocene and Eocene <strong>radiolaria</strong>n faunas were<br />
recovered from Holes 760A, 761B, 761C, and 762B. Poorly<br />
preserved Cretaceous <strong>radiolaria</strong>ns occur in samples from Holes<br />
761B, 762C, 763B, and 763C. Chert intervals from Cores 122-<br />
761B-28X, 122-761C-5R, and 122-761C-6R contain moderately<br />
well-preserved Cretaceous <strong>radiolaria</strong>n faunas (upper Albian, mid- to<br />
upper Cenomanian, and mid-Albian, respectively). Rare fragments of<br />
Upper Triassic <strong>radiolaria</strong>ns were recovered from sections in Holes<br />
759B, 760B, and 764A.<br />
The only well-preserved pre-Quaternary <strong>radiolaria</strong>ns are in<br />
lower and upper Paleocene faunas (Bekoma campechensis Zone)<br />
recovered from Site 761, Sections 122-761B-16X-1 to 122-761C-<br />
19X-CC. The composition of these faunas differs somewhat from<br />
that of isolated coeval Paleocene faunas from Deep Sea Drilling<br />
Project sites in the Atlantic, Gulf of Mexico, tropical Pacific, eastern<br />
Indian Ocean, and near Spain and North Africa, as well as from<br />
several on-land sites in North America, Cuba, and the USSR.<br />
Blome, C.D. & Reed, K.M. 1992. Permian and Early (?)<br />
Triassic <strong>radiolaria</strong>n faunas from the Grindstone Terrane,<br />
central Oregon. J. Paleont., 66/3, 351-383.<br />
Moderately well preserved Permian (late Wolfcampian,<br />
Leonardian, Guadalupian, and Djulfian) and Early(?) Triassic<br />
<strong>radiolaria</strong>n faunas from sedimentary melange cherts of the<br />
Grindstone terrane in central Oregon are nearly identical to coeval<br />
chert faunas in Japan. These Permian faunas are similar to those<br />
used in constructing the <strong>radiolaria</strong>n zonations for Japan and the<br />
Tethyan regions. Although several Oregon taxa have been reported<br />
from limestone sequences in the central United States. most of the<br />
Oregon forms have only been found in cherty rocks and nearly half<br />
have not previously been reported from North America. Forty-two<br />
taxa belonging to 19 genera (Albaillella Deflandre, Deflandrella De<br />
Wever and Caridroit, Entactinia Foreman, Entactinosphaera Foreman,<br />
Follicucullus Ormiston and Babcock, Haplentactinia Foreman,<br />
Hegleria Nazarov and Ormiston, Ishigaum De Wever and Caridroit,<br />
Kashiwara Sashida and Tonishi, Latentibifistula Nazarov and<br />
Ormiston, Latentifistula Nazarov and Ormiston, Nazarovella De<br />
Wever and Caridroit, Neoalbaillella Takemura and Nakaseko,<br />
Parentactinia Dumitrica, Praedeflandrella Kozur and Mostler,<br />
Pseudoalbaillella Holdsworth and Jones, Pseudotormentus De Wever<br />
and Caridroit, Quinqueremis Nazarov and Ormiston, and<br />
Triplanospongos Sashida and Tonishi) are systematically treated.<br />
Co-occurrences of some species in Oregon indicate that their ranges<br />
in North America may differ from those in Japan. This paper also<br />
contains the first illustrated record of Early(?) Triassic <strong>radiolaria</strong>ns<br />
from North America.<br />
Boltovskoy, D. 1992. Current and productivity patterns<br />
in the equatorial Pacific across the last glacial maximum<br />
based on <strong>radiolaria</strong>n east-west and downcore faunal gradients.<br />
Micropaleontology, 38/4, 397-413.<br />
Radiolarians were studied in 11 box-cores (142 samples in<br />
total, obtained at 3cm intervals) retrieved in the western (160°E),<br />
central ( I 35°W) and eastern (90°W) equatorial Pacific. The western<br />
and central cores span the last ca. 40,000 years, while the eastern<br />
core is estimated to reach approx. 12,000-17,000 years. Timeaveraged<br />
data show very sharp assemblage composition differences<br />
between the three locales. Species dominant at the westernmost<br />
sites are indicative of warm, oligotrophic conditions;<br />
thanatocoenoses from 135°W suggest strong input of California<br />
Current <strong>radiolaria</strong>ns; while the easternmost core hosts assemblages<br />
which point to a significant influence of the Peru Current. Downcore<br />
changes in the proportions of these three characteristic groups of<br />
species are inconclusive in the westernmost cores. In the central<br />
area the steady upcore increase in shells presumably advected from<br />
the northeastern Pacific, and the concomitant decrease of warmerwater<br />
<strong>radiolaria</strong>ns, indicate a growing influence of advection from<br />
the California Current. In the easternmost core colder-water<br />
indicators decrease from bottom to top, while those indicative of<br />
warmer waters increase, suggesting a gradual waning of advection<br />
from the Peru Current. It is concluded that, in the central and<br />
eastern parts of the equatorial Pacific belt, <strong>radiolaria</strong>n distributional<br />
patterns in the sediments and their shifts during the last millennia<br />
respond chiefly to environmental conditions at depths in excess of<br />
50m (rather than to sea surface temperature), and to subsurface<br />
and deep lateral advection of shells from eastern boundary current<br />
areas.<br />
Boltovskoy, D. & Alder, V.A. 1992a. Paleoecological<br />
implications of <strong>radiolaria</strong>n distribution and standing stocks<br />
versus accumulation rates in the Weddell Sea. In: The<br />
- 77 -<br />
Antarctic Paleoenvironment: A Perspective on Global<br />
Change. (Kennett, J.P. & Warnke, D.A., Eds.), Antarctic<br />
Research Series vol. 56. American Geophysical Union, pp.<br />
377-384.<br />
In the Scotia and Weddell Seas polycystine <strong>radiolaria</strong>ns dwell<br />
chiefly at depths between 200 and 300 m, their vertical patterns<br />
being strongly associated with the higher temperatures<br />
characteristic of the Warm Deep Water. At scales of approximately<br />
400 to 2000 km and ca. 30 days, <strong>radiolaria</strong>n horizontal quantitative<br />
distribution trends are not visibly affected by ice cover or primary<br />
production. On the other hand, comparison of polycystine standing<br />
stocks at 0-400 m vs. their accumulation rates at 400 to 900 m<br />
indicates that >90% of the shells are lost to sedimentation. It is<br />
suggested that mechanical fragmentation by grazing (rather than<br />
dissolution) is primarily responsible for this loss. Deep habitat and<br />
high destruction rates in the water-column are important factors<br />
which hinder the use of Antarctic polycystine thanatocoenoses for<br />
paleoecological reconstructions.<br />
Boltovskoy, D. & Alder, V.A. 1992b.<br />
Microzooplankton and tintinnid species-specific assemblage<br />
structures: patterns of distribution and year-to-year variation<br />
in the Weddell Sea (Antarctica). J. Plankton Res., 14, 1405-<br />
1423.<br />
Silicoflagellates, large heterotrophic dinoflagellates,<br />
<strong>radiolaria</strong>ns, tintinnids and microcrustaceans were counted in 72<br />
screened (15 µm) samples retrieved at 0-150 m from the Weddell<br />
Sea in January 1989. Tintinnid species were identified and biomass<br />
estimates were carried out for all groups on the basis of<br />
measurements of cell dimensions. Dinoflagellates dominated the<br />
microheterotrophic community at all stations and depths (65% of<br />
overall microzooplanktonic carbon in the 0-150 m interval), followed<br />
by the tintinnids (18%), microcrustaceans (16%) and <strong>radiolaria</strong>ns<br />
(1%). All groups, with the exception of silicoflagellates, peaked<br />
noticeably in the vicinity of the southern end of the transect (76-<br />
77°S). Relationships between concentrations of chlorophyll a and<br />
microzooplanktonic biomass were present, yet not altogether<br />
consistent, but both phyto- and microzooplankton seemed to<br />
generally respond to regional enhancements associated with the ice<br />
edge. Comparison with similar Weddell and Weddell-Scotia data<br />
retrieved in February-March 1987 and November 1988-December<br />
1989, respectively, are highly coherent in terms of microplanktonic<br />
abundances, their geographic and vertical distribution patterns, and<br />
the specific make-up and distribution of tintinnid assemblages.<br />
Analyses of the oral diameters of tintinnid morphotypes suggest<br />
that the latitudinal and vertical distribution of their five dominant<br />
taxa (which account for >90% of all individuals) is structured so as<br />
to maximize resource partitioning.<br />
Braun, A., Maass, R. & Schmidt-Effing, R. 1992.<br />
Oberdevonische Radiolarien aus dem Breuschtal (Nord-<br />
Vogesen, Elsas) und ihr regionaler und stratigraphischer<br />
Zusammenhang. N. Jb. Geol. Paläont. Abh., 185/2, 161-<br />
178.<br />
A well preserved Radiolarian fauna (Uppermost Devonian, 13<br />
species resp. forms) from a sequence of Greywackes and<br />
Radiolarites of the Breuschtal is figured and described. The fauna is<br />
discussed in its relation to the Devonian and Lower Carboniferous<br />
sedimentary sequence on the basis of results of detailed field<br />
mapping. It is possible to improve the correlation of single<br />
tectonically isolated sequences of sedimentary rocks showing<br />
different facies in this area.<br />
Caridroit, M., Vachard, D. & Fontaine, H. 1992.<br />
Datations par radiolaires (Carbonifère, Permien et Trias) en<br />
Thailande nord-occidentale. Mise en évidence de nappes de<br />
charriage et d'olistostromes. C.R. Acad. Sci. (Paris), Sér. II,<br />
315/4, 515-520.<br />
The classical Paleozoic stratigraphic column In NW Thailand<br />
was described as a single Ordovician to Permian marine succession<br />
(including undated radiolarites) considered to be tectonized in<br />
Triassic time. Ages obtained from radiolarite dating (Carboniferous<br />
to Triassic) demonstrate the existence of a separated sedimentary<br />
basin far from detritic sources and far from the deposition area of<br />
the Carboniferous to Triassic limestones. The present structural<br />
imbrication of radiolarites with limestones and detritic series is<br />
interpreted in terms of tectonic nappes with considerable shortening<br />
and olistostrome deposits.<br />
Catalano, R., Di Stefano, P. & Kozur, H. 1992.<br />
New data on Permian and Triassic stratigraphy of Western<br />
Sicily. N. Jb. Geol. Paläont. Abh., 184/1, 25-61.
Bibliography - 1992 Radiolaria 14<br />
The Sicanian paleogeographic domain (Western Sicily) belonged,<br />
at least since the Early Permian, to the passive margin of the Tethys<br />
ocean. Continuous pelagic deep-water conditions throughout the<br />
Permian and the presence of rich pelagic Circumpacific faunas of<br />
this age indicate a broad, unrestricted pelagic connection from the<br />
Pacific (Panthalassa) until Western Sicily at least since the Early<br />
Permian. During the Triassic, pelagic conditions continued. The<br />
paleogeographic restriction of the ecologically tolerant conodont<br />
genus Pseudofurnishius to originally southern units within the Tethys<br />
has been confirmed.<br />
Caulet, J.P., Venec-Peyre, M.-T., Vergnaud-<br />
Grazzini, C. & Nigrini, C. 1992. Variation of South<br />
Somalian upwelling during the last 160 ka: <strong>radiolaria</strong>n and<br />
foraminifera records in core MD 85674. In: Upwelling<br />
Systems: Evolution Since the Early Miocene. (Summerhayes,<br />
C.P., Prell, W.L. & Emeis, K.C., Eds.), vol. 64. Geological<br />
Society of London, special Publication, London, U. K. pp.<br />
379-389.<br />
Indicators of upwelling activity and surface-water productivity<br />
for the last 160 ka have been studied in the 'Marion Dufresne' core<br />
MD 85674 taken off Somalia (3°11, 2 N-50°26, 3 E; 4875 m<br />
depth). Quantitative changes in the abundances of <strong>radiolaria</strong>n<br />
species which are restricted to upwelling areas (A. murrayana, C.<br />
irregularis, D. infabricatus, L. nigriniae, P. caryoforma, P. crustula<br />
and P. minythorax) were used to monitor the variation of vertical<br />
advection of deep water. These changes are compared with those<br />
recorded by the stable carbon isotopes of a foraminiferal<br />
thermocline dweller, N. dutertrei, and with quantitative variations of<br />
some planktonic foraminifers (N. dutertrei, G. bulloides, C. menardii,<br />
G. sacculifer and G. glutinata). Taken together, our data indicate<br />
that, under the south Somalian gyre, upwelling activity was maximal<br />
during transition between isotope stages 6 and 5, isotope stage 3,<br />
and transition between isotope stages 2 and 1 (respectively at<br />
about 130 ka, 65 to 25 ka. and 15 to 10 ka). These data also<br />
suggest that. at least during the last 60 ka. periods of increased<br />
activity in the Somalian. Arabian and Peruvian upwelling systems<br />
were synchronous.<br />
Cheng, Y.N. 1992. Upper Jurassic Pantanelliidae<br />
(Pantanelliinae Pessagno,1977 and Vallupinae Pessagno &<br />
MacLeod, 1987) from the Busuanga Islands, Philippines.<br />
Bull. natl. Mus. nat. Sci., Taiwan, 3, 1-49.<br />
The Pantanelliidae Pessagno is an important Mesozoic family of<br />
Liosphaerilae. Pantanelliids are proved to be useful in<br />
paleogeographic interpretation. They are abundant and diversified<br />
within the Tethyan Realm and become rare and less diversified within<br />
the Boreal Realm.<br />
This report deals with the systematic paleontology of Upper<br />
Jurassic (Tithonian) pantanelliids from the Liminangcong Chert of<br />
Busuanga Island, North Palawan Block, Philippines. Radiolarian<br />
assemblages ranging in age from Permian to Jurassic have been<br />
discovered from the Liminangcong Chert. The studied material is<br />
from the youngest samples (upper Tithonian) from the Liminangcong<br />
Chert in Busuanga. It is characterized by having Tethyan<br />
pantanelliids. Radiolarian individuals are relatively small in size by<br />
comparing with those from the upper Tithonian North American<br />
strata (e.g., Taman Formation, east-central Mexico).<br />
Taxa of two subfamilies -- Pantanelliinae Pessagno (1977) and<br />
Vallupinae Pessagno & MacLeod (1987) are described in this report.<br />
These include 16 new species of genus Pantanellium Pessagno<br />
(1977), six new species of genus Mesovallupus Pessagno and<br />
MacLeod (1987), nine new species of genus Protovallupus Pessagno<br />
and MacLeod (1987), and one new species of Vallupus Pessagno and<br />
Blome (1984).<br />
Coccioni, R., Erba, E. & Premoli-Silva, I. 1992.<br />
Barremian-Aptian calcareous plankton biostratigraphy from<br />
the Gorgo Cerbara section (Marche, central Italy) and<br />
implications for plankton evolution. Cretaceous Res., 13/5-<br />
6, 517-538.<br />
The Barremian-Aptian boundary interval of the Gorgo Cerbara<br />
section (Marche, central Italy) was revisited in order to improve<br />
stratigraphic correlations and investigate plankton evolution. A very<br />
close sampling at cm scale was carried out in the upper Maiolica and<br />
basal Scisti a Fucoidi formations. The latter formation includes the<br />
Livello Selli, the landward sedimentary expression of oceanic anoxic<br />
subevent OAE la. The study of closely spaced samples revealed that<br />
(I) the first diversification among planktonic foraminifera, marked by<br />
the appearance of the genus Globigerinelloides, occurred during the<br />
Barremian (this event was dated by means of ammonites); thus the<br />
first occurrence (FO) of both Globigerinelloides duboisi and<br />
Globigerinelloides blowi cannot be used to identify the Aptian (2) the<br />
appearance of Rucinolithus irregularis is the biostratigraphic event<br />
- 78 -<br />
which best approximates the Barremian-Aptian boundary; and (3)<br />
chron M0, being slightly younger than the FO of R. irregularis, is very<br />
close to this boundary. Semiquantitative and quantitative analyses<br />
of planktonic foraminifera, calcareous nannofossils and <strong>radiolaria</strong>ns<br />
show that the three groups fluctuate in abundance and assemblage<br />
composition throughout the studied interval. An important change in<br />
plankton distribution patterns occurs within the G. blowi<br />
foraminiferal Zone and C. Iitterarius nannofossil Zone, where<br />
planktonic foraminifera, <strong>radiolaria</strong>ns and calcareous nannofossils<br />
start to show large-scale, higher frequency fluctuations in<br />
abundance; fluctuations in the three groups are out of phase. These<br />
new plankton distribution patterns are interrupted by the Livello<br />
Selli, which is preceded and followed by 'critical intervals'. The<br />
distribution and composition of all three planktonic groups lead to<br />
the interpretation of the 'critical intervals' as representing<br />
increased nutrient contents in the surface water and the Livello Selli<br />
as a very high fertility event. Among planktonic foraminifera the<br />
hedbergellids seem to indicate a more eutrophic habitat than the<br />
globigerinelloids. In calcareous nannofossil assemblages, the abrupt<br />
crisis affecting the nannoconids prior to deposition of the Livello<br />
Selli suggests that these nannofossils are characteristic of more<br />
oligotrophic conditions, whereas Zygodiscus erectus is indicative of<br />
a more eutrophic environment. Based on our data, the early Aptian<br />
Livello Selli has the same oceanographic significance as the latest<br />
Cenomanian Livello Bonarelli, i.e., it represents a high fertility event<br />
on a global scale.<br />
Conti, M. & Marcucci, M. 1992. Radiolarian dating of<br />
the Monte Alpe Chert at Il Conventino, Monti Rognosi<br />
(Eastern Tuscany, Italy). Ofioliti, 17/2, 243-248.<br />
This paper reports new data on <strong>radiolaria</strong>n biostratigraphy of<br />
the siliceous deposits in the sedimentary cover of the Apennine<br />
ophiolites. Earlier studies on this subject (Baumgartner, 1984; Conti<br />
et al., 1985; Picchi, 1985; Abbate et al., 1986; Conti and Marcucci,<br />
1991) permit to determine ages ranging from late Bathonian (?) -<br />
early Callovian to late Oxfordian-Kimmeridgian for the base of these<br />
deposits. Their top is late Tithonian to Berriasian.<br />
The sections described here are in the Northern Apennine, and<br />
belong to the Monte Alpe Chert, which is the main siliceous<br />
formation on top of the ophiolites in this region. These sections<br />
outcrop at Monti Rognosi (Eastern Tuscany) where the ophiolites,<br />
with their sedimentary cover, are considered to be olistoliths<br />
included in an Eocene flysch formation (M. Morello Formation)<br />
(Bortolotti, 1961; 1962; Sarri, 1990). This formation is part of the<br />
Calvana Supergroup which constitutes one of the major tectonic<br />
units of the Northern Apennine.<br />
Cordey, F. 1992a. Radiolarian ages from chert pebbles of<br />
the Tantalus Formation, Carmacks area, Yukon Territory.<br />
Geol. Surv. Canada, curr. res., Pap., 92-1E, 53-59.<br />
Eighteen chert pebbles from three levels of the Late Jurassic-<br />
Cretaceous Tantalus Formation conglomerate near Carmacks<br />
contain <strong>radiolaria</strong> of Triassic (Ladinian-Carnian, Late Carnian-Middle<br />
Norian, Middle Norian, Late Norian) age. The known ages of chert<br />
pebbles from the Tantalus Formation near Whitehorse and<br />
Carmacks, which range from the Early Permian to the latest Triassic,<br />
differ from the age of Paleozoic chert-bearing units located to the<br />
northeast of the Tintina Fault. They more closely resemble the age of<br />
ribbon cherts of the northeastern part of the Northern Cache Creek<br />
Terrane (Teslin Plateau) in southern Yukon.<br />
Cordey, F. 1992b. Radiolarians and terrane analysis in the<br />
Canadian Cordillera: the "clastic approach". In: Significance<br />
and application of Radiolaria to terrane analysis. (Aitchison,<br />
J.C. & Murchey, B.L., Eds.), vol. 96/1-2. Special Issue:<br />
Palaeogeogr. Palaeoclimatol. Palaeoecol., Elsevier,<br />
Amsterdam. pp. 155-159.<br />
The Canadian Cordillera is characterized by a long-lived<br />
geological history resulting from protracted interaction of oceanic<br />
plates and one large continent. Interpreted as a "collage" orogen, it<br />
contains terranes of oceanic affinity separating volcanosedimentary<br />
blocks. Oceanic, <strong>radiolaria</strong>n chert-bearing accreted<br />
terranes are important structural markers and age control of their<br />
sedimentary strata is fundamental to the understanding of a<br />
complex geological history. Synorogenic and postorogenic deposits<br />
contain <strong>radiolaria</strong>n chert clasts, which allow correlations with strata<br />
in place. More interestingly, they also contain eroded strata that are<br />
unknown in the Cordillera. Radiolarians appear to be the key in the<br />
potential discovery of such missing elements of the geological<br />
record.<br />
Cordey, F., Greig, C.J. & Orchard, M.J. 1992.<br />
Permian, Triassic, and Middle Jurassic microfaunal<br />
associations, Stikine terrane, Oweegee and Kinskuch areas,
Radiolaria 14 Bibliography - 1992<br />
northwestern British Columbia. Geol. Surv. Canada, curr.<br />
res., Pap., 92-1E, 107-116.<br />
Nine age-diagnostic microfossil collections from the Stikine<br />
terrane in northwestern British Columbia confirm the presence and<br />
extend the distribution of several regionally mappable geological<br />
units; they also place constraints on the timing of early Mesozoic<br />
deformation affecting western Stikine terrane. Radiolarians are Early<br />
Permian, Late Triassic, and Middle Jurassic in age, spanning a large<br />
part of the stratigraphic range of Stikine terrane, and are found in<br />
various lithologies, including siliceous siltstone, limestone, and<br />
bedded chert. Conodonts are from carbonate and are Late Triassic<br />
(Late Carnian, Late Norian) in age.<br />
Cordey, F. & Read, P.B. 1992. Permian and Triassic<br />
<strong>radiolaria</strong>n ages from the Cache Creek Complex, Dog Creek<br />
and Alkali Lake areas, southwestern British Columbia. Geol.<br />
Surv. Canada, curr. res., Pap., 92-1E, 41-51.<br />
Ten <strong>radiolaria</strong>n chert localities from the Cache Creek Complex<br />
on both sides of the Fraser Fault in Dog Creek and Alkali Lake areas<br />
range in age from Early Permian (late Asselian-late Sakmarian)<br />
through Middle Triassic (late Anisian-early Ladinian) to Late Triassic<br />
(Early Carnian, Early-Middle Norian, Late Norian). This age range is<br />
similar to that of the Cache Creek cherts in their type locality, 150<br />
km to the south. The newly discovered localities come from one or<br />
more slices of the complex which were thrust northeastward over<br />
Early Jurassic rocks. Chert-bearing units underlie undated clastic<br />
rocks that may represent a regional(?) overlap assemblage.<br />
Diester-Haass, L., Meyers, P.A. & Rothe, P.<br />
1992. The Benguela Current and associated upwelling on the<br />
southwest African Margin: a synthesis of the Neogene-<br />
Quaternary sedimentary record at DSDP sites 362 and 532. In:<br />
Upwelling Systems: Evolution Since the Early Miocene.<br />
(Summerhayes, C.P., Prell, W.L. & Emeis, K.C., Eds.), vol.<br />
64. Geological Society of London, special Publication,<br />
London, U.K. pp. 331-342.<br />
Sediments cored at DSDP Sites 362 and 532 on the Walvis<br />
Ridge provide a Neogene-Quaternary history of the development of<br />
the upwelling system on the south-west African margin. Upwelling<br />
occurs principally on the landward side of the Benguela Current. The<br />
upwelling centres have shifted northward since the Middle Miocene<br />
as the current has intensified and has flowed farther to the north.<br />
Changes in productivity are recorded in the types, proportions and<br />
preservation of foraminifera, <strong>radiolaria</strong>, diatoms, organic matter, and<br />
clay minerals in the sedimentary record. Prior to the Late Miocene<br />
(10 Ma), the Benguela Current did not reach the Walvis Ridge, and<br />
enhanced productivity is not evident in the sediments at this<br />
location. Between 10 to 5.2 Ma, upwelling was recorded in the DSDP<br />
sites in glacial periods, indicating that the Benguela Current<br />
intensified during glacial periods and transported evidence of<br />
upwelling to Sites 362/532 from near-coastal areas. During<br />
interglacial periods the current was not as strong and did not reach<br />
the Walvis Ridge, turning instead to the west within the Cape Basin.<br />
Strengthening of the current continued such that by the Pliocene and<br />
Quarternary the upwelling signal is contained in interglacial<br />
sediments. Sediments deposited in these more recent glacial times<br />
contain a weak or absent upwelling signal because glacial<br />
intensification shifts the Benguela Current system northward to<br />
reach the Angola Basin before it turns westward away from its<br />
coast-parallel direction.<br />
El Kadiri, K. 1992. Description de nouvelles espèces de<br />
radiolaires jurassiques de la Dorsale calcaire externe (Rif,<br />
Maroc). Rev. españ. Paleont., Núm. Extra., 37-48.<br />
The study of <strong>radiolaria</strong> obtained from the bottom of the Jurassic<br />
<strong>radiolaria</strong>n beds in the Rif "Dorsale calcaire externe" display the<br />
study of some new species. Some one and two new genres are<br />
described here. The presence of ammonites in the bottom of that<br />
facies and the inmediately in the lower beds attribute an Upper Lias<br />
or Lower Dogger age to the siliceous micro-faune recolted.<br />
El Kadiri, K., Linares, A. & Olóriz, F. 1992. La<br />
Dorsale Calcaire rifaine (Maroc septentrional): Evolution<br />
stratigraphique et géodynamique durant le Jurassique-Crétacé.<br />
Notes Mém. Serv géol. Maroc, 366, 217-265.<br />
The reduced Jurassic-Cretaceous series of the "Dorsale<br />
calcaire" with facies of ammonitico-rosso type and radiolarites are<br />
dated by the main chronological markers: ammonites, Radiolaria,<br />
Calpionellids and Foraminifera. The stratigraphic and geodynamic<br />
evolution of the "Dorsale interne" appears to be clearly different<br />
from that of the "Dorsale externe". In the first one, significant<br />
episodes of emersion-karstification are made evident during the<br />
Carixian, Dogger-Malm p.p. and the Cretaceous p. p. During the time<br />
- 79 -<br />
between these episodes a reduced sedimentation which is preserved<br />
in the paleokarstic cavities is expressed in the form of: 1)<br />
ammonitico-rosso facies during the Domerian-Toarcian, 2)<br />
radiolarites during the upper kimmeridgian-lower Tithonian and 3)<br />
ammonitico-rosso/bianco during the Tithonian. At the end of the<br />
Cretaceous the sedimentation starts again by the deposition<br />
olistostromes during the Campanian. While the Jurassic<br />
sedimentation in the "Dorsale externe" remains almost continuous.<br />
Moreover, these different facies appear early: ammonitico-rosso<br />
facies from the end of the Hettangian and continue during the<br />
Sinemurian; radiolarites from the upper Toarcian-Aalenian. The<br />
Olistostromes appear from the lower Cretaceous.<br />
These reduced series which have to do with a subsiding<br />
continental margin show that the "Dorsale interne" and "Dorsale<br />
externe" correspond respectively: 1) to one or several half-grabens<br />
tilted towards the internal side of the margin and 2) to crustal<br />
blocks located at distal position. The relative movement of the<br />
internal half-grabens in relation to the external blocks leads us to<br />
put forward a kinematic model for the dynamics of the subsiding<br />
continental margin: the movement of the balance. The global context<br />
of this movement was the normal shearing of the crust.<br />
The application of this model to the westhern front of the<br />
Alboran plate (Rif) allows us to propose the existence of: 1) a basal<br />
intralithospheric fault at the old boundary between the internal and<br />
the external Zones diping towards the East, and 2) an astenospheric<br />
dome which emerges below the Alboran plate starting from the lower<br />
Lias.<br />
Feng, Q. 1992. Permian and Triassic <strong>radiolaria</strong>n<br />
biostratigraphy in south and southwest China. Earth Sci., J.<br />
China Univ. Geosci., 3/1, 51-62.<br />
The study of Permian <strong>radiolaria</strong>ns in South and Southwest China<br />
has been advanced in recent years . A well—preserved <strong>radiolaria</strong>n<br />
fauna of Triassic is recently found in Southwest China. Eight<br />
<strong>radiolaria</strong>n assemblage zones are recognized as follows in ascending<br />
order: Pseudoalbaillella rhombothoracata assemblage zone (Qixian),<br />
Pseudoalbaillella fusiformis assemblage zone (early—middle<br />
Maokouan), Follicucullus assemblage zone (late Maokouan-<br />
Wujiapingian). Cangyuanella assemblage zone (early—middle<br />
Changxingian), Clavata assemblage zone (latest Permian),<br />
Triassocampe yini assemblage zone (early Early Triassic),<br />
Pseudoeucyrtis liui assemblage zone (late Early Triassic) and<br />
Triassocampe deweveri assemblage zone (Middle Triassic) .The<br />
Permo—Triassic boundary in chert mono—facial sequence of the<br />
Muyinhe Formation is discussed.<br />
Goto, H., Umeda, M. & Ishiga, H. 1992. Late<br />
Ordovician Radiolarians from the Lachlan Fold Belt,<br />
Southeastern Australia. Mem. Fac. Sci., Shimane Univ., 26,<br />
145-170.<br />
Gowing, M.M. & Garrison, D.L. 1992. Abundance<br />
and feeding ecology of larger protozooplankton in the iceedge<br />
zone of the Weddell and Scotia Seas during the austral<br />
winter. Deep-Sea Res. Part A, oceanogr. Res. Pap., 39, 893-<br />
919.<br />
Biomass abundances and feeding ecology of larger (>50µm<br />
diameter) protozoo plankton were studied in the upper 210 m in the<br />
ice edge zone of the Weddell/Scotia Sea area in the austral winter of<br />
1988. Sixty -liter water samples were taken at five depths at 17<br />
stations, and organisms were concentrated by reverse flowfiltration.<br />
Mean abundances of the total assemblages of larger<br />
protozooplankton (<strong>radiolaria</strong>ns, foraminiferans, acantharian, the<br />
heliozoan Sticholonche, tintinnid and aloricate ciliates, and thecate<br />
and athecate dinoflagellates) ranged from 2040 to 3745 m -3 in the<br />
upper 210m. Biomass ranged from 33 to 48 µg C m -3 in the upper<br />
85 m, and from 32 to 54 µg C m -3 from 115 to 210 m. Phaeodarian<br />
<strong>radiolaria</strong>ns larger than 1.6 mm (sampled with plummet nets)<br />
contributed an additional 3 µg C m -3 in the upper 100 m and an<br />
additional 7 µg C m -3 from 100 to 200 m. These abundances and<br />
biomasses are lower than for other seasons in the Antarctic, but are<br />
comparable to abundances reported for several of these groups in<br />
lower latitude waters. We attribute the low winter abundances to<br />
slower growth and reduced food, rather than to increased mortality.<br />
The large protozooplankton are trophically diverse; in addition to<br />
heterotrophy on a variety of organisms, we found apparent evidence<br />
of mixotrophy and symbiosis in some of the groups. The large<br />
protozooplankton fed on both autotrophic and heterotrophic<br />
organisms in winter, although the biomass of smaller forms is<br />
dominated by heterotrophs. Feeding on detrital particles also was<br />
indicated by the presence of siliceous fragments in vacuoles. The<br />
larger particles also was indicated by the presence of siliceous<br />
fragments in vacuoles. The larger protozooplankton in the winter ice<br />
edge zone may be important in reducing particle flux to the deep sea<br />
and as a food source for larger zooplankton, especially form the<br />
base of the euphotic zone to 210 m.
Bibliography - 1992 Radiolaria 14<br />
Guex, J. 1992. Origine des sauts évolutifs chez les<br />
ammonites. Bull. Soc. vaud. Sc. nat., 82/2, 117-144.<br />
Ammonoid lineages frequently start with evolute<br />
representatives which become more involute during their evolution.<br />
From a geometrical point of view, this trend can be regarded as an<br />
increase of the dimensionality of the shells. During periods of<br />
ecological stress, this trend is often reversed. In extreme cases,<br />
some end-forms can generate new groups which are globally<br />
simplified and of atavistic aspect. Such atavistic groups are the<br />
source of new evolutionary lineages. Temporal variations in the<br />
morphological complexity of ammonites are compared with those<br />
known in some other groups of invertebrates (i.e.:Radiolaria,<br />
Foraminifera).<br />
Gupta, S.M. & Srinivasan, M.S. 1992. Late Miocene<br />
<strong>radiolaria</strong>n biostratigraphy and paleoceanography of Sawai<br />
Bay Formation, Neill Island, Andamans, India.<br />
Micropaleontology, 38/3, 209-235.<br />
Stichocorys peregrina Didymocyrtis penulrima and<br />
Didymocyrtis antepenultima Late Miocene <strong>radiolaria</strong>n zones are<br />
encountered from mudstone strata of Sawai Bay Formation, Neill<br />
Island, Andamans. Percentage data of forty-five coarser taxonomic<br />
groups of <strong>radiolaria</strong>ns were subjected to Q-mode cluster analysis.<br />
Cluster A comprises Stichocorys, Phormospyris, Eucyrtidium,<br />
Lamprocyclas, Acrosphaera and Cycladophora groups. Cluster B was<br />
divided into subclusters at 0.83 level of clustering. Subcluster B1<br />
comprised Didymocyrtis-Diartus, Pyloniids, Collosphaera,<br />
Phacodiscids, Pterocorythids, Pterocanium and Spongodiscids,<br />
whereas subcluster B2 comprised Porodiscus, Euchitonids,<br />
Stylodictya-Stylochlamydium, Spongopyle, Phormostichoartus,<br />
Lophophaenids and Lithelius groups.<br />
Based on the ecology of the modern homeomorphs of the<br />
dominant <strong>radiolaria</strong>n groups, it is suggested that cluster A and<br />
cluster B indicate colder and warmer periods, respectively.<br />
Subcluster Bl indicates surface-water fauna and subcluster B2<br />
represents subsurface water fauna. Dominance of subcluster B2 in<br />
Didymocyrtis antepenultima zone (8.5-7.2 Ma) suggests that<br />
subsurface fauna was thriving more probably due to the monsoonal<br />
upwelling during warmer periods. This finding is also substantiated<br />
with diatom/<strong>radiolaria</strong> ratio. Presence and absence of deep (1200-<br />
2000m) and intermediate (700-1200m) water dwelling <strong>radiolaria</strong>ns<br />
like the Plectopyramids, Botryostrobus and Sethoperinids groups<br />
indicate basinal shallowing during Late Miocene. It may be due to<br />
subduction of the Indian plate below the Asian plate, coupled with<br />
huge sediment discharged from the Irrawaddy River of Burma during<br />
monsoon dominated warmer periods (5.0-6.3 and 8.5-7.7 Ma) in<br />
Late Miocene.<br />
Hada, S., Sato, E., Takeshima, H. & Kawakami,<br />
A. 1992. Age of the covering strata in the Kurosegawa<br />
Terrane: dismembered continental fragment in southwest<br />
Japan. In: Significance and application of Radiolaria to<br />
terrane analysis. (Aitchison, J.C. & Murchey, B.L., Eds.),<br />
vol. 96/1-2. Special Issue: Palaeogeogr. Palaeoclimatol.<br />
Palaeoecol., Elsevier, Amsterdam. pp. 59-70.<br />
Along with the rapid development of <strong>radiolaria</strong>n biostratigraphy,<br />
introduction of the new concept of tectonostratigraphic terranes has<br />
urged us to reexamine "geosynclinal complexes" which contain<br />
various <strong>radiolaria</strong>n-rich rocks such as fine-grained clastic, siliceous,<br />
and tuffaceous rocks. Entirely new age data have been discovered<br />
from these hitherto poorly known formations. However, until<br />
recently, little attention has been paid to the age of geologic units<br />
consisting mainly of orderly stratigraphic sequences and coarsegrained<br />
clastic rocks such as the "Usuginu-type Conglomerate" in<br />
the Kurosegawa terrane, which is characterized by the presence of<br />
abundant clasts of granitic rocks. Accurate dating of conglomeratebearing<br />
formations in the Kurosegawa terrane using <strong>radiolaria</strong>n<br />
fossils provides a basis for tectonic reconstructions of the<br />
Kurosegawa terrane. These formations are fairly well-bedded<br />
sequences of mudstone, sandstone and conglomerate, without any<br />
exotic clasts of oceanic affinity. They range in age from mid-Permian<br />
to Middle Jurassic. Integration of these results indicates that the<br />
Kurosegawa terrane originated as a fragment of continental margin<br />
characterized by the presence of crystalline basement and coherent<br />
covering strata. However, the elements of the Kurosegawa terrane<br />
were subsequently severely disrupted into a zone of melange.<br />
Harms, T.A. & Murchey, B.L. 1992. Setting and<br />
occurrence of Late Paleozoic <strong>radiolaria</strong>ns in the Sylvester<br />
allochthon, part of the proto-Pacific ocean floor terrane in<br />
the Canadian Cordillera. In: Significance and application of<br />
Radiolaria to terrane analysis. (Aitchison, J.C. & Murchey,<br />
B.L., Eds.), vol. 96/1-2. Special Issue: Palaeogeogr.<br />
- 80 -<br />
Palaeoclimatol. Palaeoecol., Elsevier, Amsterdam. pp. 127-<br />
139.<br />
Late Paleozoic <strong>radiolaria</strong>ns have been used to establish the<br />
ages or age ranges of fourteen lithotectonic units in the Sylvester<br />
allochthon of the Slide Mountain terrane in British Columbia, and<br />
have thereby greatly clarified the geology and tectonic history of the<br />
terrane. As the Sylvester <strong>radiolaria</strong>n fauna is limited, age<br />
assignments were based on a few distinctive and diagnostic robust<br />
forms. Radiolarians occur in cherts from a wide variety of different<br />
oceanic sequences that are structurally juxtaposed within the<br />
Sylvester allochthon. Like others in a suite of correlative terranes<br />
that lie along the length of the Cordillera, the Sylvester allochthon<br />
and the <strong>radiolaria</strong>n bearing cherts in it derive from the telescoping<br />
together of slices from what was, in the late Paleozoic, a large area<br />
of the proto-Pacific ocean.<br />
Hashimoto, H. & Ishida, K. 1992. The <strong>radiolaria</strong>n<br />
assemblages and its age from the Sotoizumi Group, eastern<br />
Shikoku. J. geol. Soc. Japan, 98/1, 61-63. (in Japanese)<br />
Haslett, S. 1992. Early Pleistocene glacial-interglacial<br />
<strong>radiolaria</strong>n assemblages from the eastern equatorial Pacific. J.<br />
Plankton Res., 14/11, 1553-1563.<br />
Polycystine <strong>radiolaria</strong> from ODP Hole 677A in the eastern<br />
equatorial Pacific were examined at isotopically identified Early<br />
Pleistocene glacial maxima and minima. Two distinct <strong>radiolaria</strong>n<br />
assemblages are recognized, characterizing glacial and interglacial<br />
optima. The Glacial Assemblage is characterized by high abundances<br />
of Theocalyptra davisiana, Botryostrobus auritus, Anthocyrtidium<br />
zanguebaricum and Hexacontium enthacanthum. The Interglacial<br />
Assemblage is characterized by Tetrapyle octacantha, Octapyle<br />
stenozoa and Theocorythium vetulum. A comparison of these fossil<br />
assemblages with modern <strong>radiolaria</strong>n distribution suggests that the<br />
Glacial Assemblage represents intensified upwelling of cold<br />
advected water via the Eastern Pacific Boundary Current, whilst the<br />
Interglacial Assemblage indicates climatic amelioration in the<br />
eastern equatorial Pacific, with the prevalence of warm (>21°C)<br />
tropical/subtropical surface waters. The recognition of these<br />
<strong>radiolaria</strong>n assemblages could be successfully applied to studies of<br />
adjacent east Pacific areas where other palaeoecological indicators<br />
are lacking.<br />
Hirano, H., Tanabe, K., Ando, H. & Futakami, M.<br />
1992. Cretaceous forearc basin of Central Hokkaido:<br />
lithofacies and biofacies characteristics. In: Paleozoic and<br />
Mesozoic Terranes: Basement of the Japanese Island Arcs.<br />
29th IGC Field Trip Guide Book. (Adachi, M. & Suzuki, K.,<br />
Eds.), vol. 1. Nagoya University, Nagoya, Japan. pp. 45-80.<br />
Hisada, K., Igo, H. & Arai, S. 1992. Mesozoic<br />
melanges and associated rocks in the Kanto mountains. In:<br />
Paleozoic and Mesozoic Terranes: Basement of the Japanese<br />
Island Arcs. 29th IGC Field Trip Guide Book. (Adachi, M. &<br />
Suzuki, K., Eds.), vol. 1. Nagoya University, Nagoya,<br />
Japan. pp. 115-141.<br />
Hisada, K.I., Karata, Y. & Kishida, Y. 1992.<br />
Geology of the Yasudo area, northeastern part of the Kanto<br />
mountains, central Japan. Annu. Rep. Inst. Geosci., Univ.<br />
Tsukuba, 18, 53-58.<br />
The northwest trending Chichibu Paleozoic- Mesozoic<br />
sedimentary complex is widely underlain in the Chichibu terrane of<br />
the Kanto mountains (Fig. 1). The Chichibu terrane is bounded on the<br />
north by the Sambagawa high P/T type metamorphic rocks and on the<br />
south by the Shimanto sedimentary complex terranes. The Shimanto<br />
complex, which is composed of Cretaceous and Paleogene sandy<br />
flysch and melange-like disturbed beds, is in fault contact with the<br />
Chichibu complex. This fault has been traditionally called the<br />
Butsuzo tectonic line and considered to be a southward vergent<br />
thrust. The Sambagawa terrane comprises two-fold stratigraphic<br />
units, namely the Mikabu green rocks in the upper part and the<br />
Sambagawa crystalline schist in the lower. The Mikabu green rocks<br />
usually occur just to the north of the Chichibu complex, and the<br />
stratigraphical relationship between them was reported by some<br />
authors (e.g. Uchida, 1981; Hisada, 1984). Their interpretations are<br />
variously offered.<br />
In the geologic map of the Kanto mountains (Fig. 1), it can be<br />
recognized that the north-south width of the Sambagawa<br />
metamorphic terrane widens remarkably in the Yasudo area, the<br />
northeastern corner of the Kanto mountains, and that the Chichibu<br />
sedimentary complex isolately crops out within the exposure area of<br />
the Sambagawa terrane. This peculiar distributional pattern is an<br />
interesting problem from the viewpoint of stratigraphy and
Radiolaria 14 Bibliography - 1992<br />
structural geology of the Chichibu and Sambagawa terranes in the<br />
Kanto mountains. We already presented two papers relating the<br />
stratigraphy and structural geology to the south of the Yasudo area<br />
(Hisada and Kishida, 1988; Hisada 1989). In this paper, we will deal<br />
with the stratigraphy of the Chichibu sedimentary complex in the<br />
Yasudo area and discuss the structural implications.<br />
Hisada, K.I., Ueno, H. & Igo, H. 1992. Geology of<br />
the Upper Paleozoic and Mesozoic sedimentary complex of<br />
the Mt Ryokami area in the Kanto Mountains, central Japan.<br />
Sci. Rep. Inst. Geosci., Univ. Tsukuba, Sect. B: geol. Sci.,<br />
13, 127-151.<br />
The Upper Paleozoic and Mesozoic sedimentary complex<br />
constituting the Chichibu terrane extensively crops out in the Mt.<br />
Ryokami area of the Kanto Mountains. This complex comprises the<br />
Nakatsugawa Group including four tectonostratigraphic units, such<br />
as the Nogurizawa. Ryokami. Ogamata, and Ryokami-yama chert.<br />
Early to Middle Jurassic <strong>radiolaria</strong>ns were recovered from shaly<br />
matrix of these units except for the last unit.<br />
The Nogurizawa unit is subdivided into five subunits, α to ε, and<br />
composed mainly of chaotic rocks consisting of chert, greenstone,<br />
and others with shaly matrix, which yielded the <strong>radiolaria</strong>ns of the<br />
Parahsuum simplum Zone-Tricolocapsa conexa Zone. The Ryokami<br />
unit consists mainly of chaotic rocks characterized by frequent<br />
association of fusulinacean limestone blocks. The shaly matrix of<br />
the Ryokami yielded the <strong>radiolaria</strong>ns assigned to the Tricolocapsa<br />
plicarum Zone. The Ogamata unit is composed mainly of sandstone<br />
intercalating thick chert blocks and subdivided into α and β subunits.<br />
The shaly matrix of the Ogamata yielded the <strong>radiolaria</strong>ns. which are<br />
correlative to the Tricolocapsa plicarum Zone to T. conexa Zone. The<br />
Ryokami-yama chert units consists mainly of chert with frequent<br />
intercalations of greenstone and thrust over other underlying units.<br />
Thick chert of this unit yielded Permian <strong>radiolaria</strong>ns as well as<br />
Triassic and Early Jurassic ones.<br />
Sedimentological and structural geologic data suggest that the<br />
Nogunzawa Group constitutes the Mesozoic accretionary wedge.<br />
Namely, chaotic rocks assignable to melange may be produced in<br />
various settings on or within as accretionary wedge.<br />
Holdsworth, B.K. & Nell, A.R. 1992. Mesozoic<br />
<strong>radiolaria</strong>n faunas from the Antarctic Peninsula: age,<br />
tectonics and palaeoceanographic significance. J. geol. Soc.<br />
London, 149/6, 1003-1020.<br />
New assemblages of Radiolaria, including some of the few<br />
occurrences of high southern latitude Jurassic and Cretaceous<br />
<strong>radiolaria</strong>n faunas, show that several localities in the LeMay Group<br />
of Alexander Island range in age from latest Jurassic earliest<br />
Cretaceous to at least Albian. By demonstrating that sedimentation<br />
and deformation in the LeMay Group was diachronous, younging<br />
oceanwards to the northwest, these new age assessments support<br />
the model of the LeMay Group as an accretionary complex. The<br />
polarity of subduction beneath Alexander Island was not affected by<br />
arc collisions from at least the Lower Jurassic to the Oligocene, and<br />
such a long period of continuous accretion appears to be unusual.<br />
Deposition of the LeMay Group spans the Kimmeridgian to Albian<br />
sedimentation in the Fossil Bluff Group fore-arc basin, thus making<br />
the earlier concept of the LeMay Group as pre-Jurassic 'basement'<br />
untenable.<br />
Allochthonous latest Jurassic-earliest Cretaceous <strong>radiolaria</strong>n<br />
assemblages with some supposed Tethyan affinities are present in<br />
the LeMay Group. In contrast, an in situ latest Jurassic assemblage<br />
from the Nordenskjöld Formation of the back-arc basin and a further<br />
Jurassic assemblage from a probable trench-slope basin have<br />
characteristics believed diagnostic of high latitudes. The<br />
biogeographic affinities of <strong>radiolaria</strong>ns from cherts in the LeMay<br />
Group accretionary complex suggest that both these cherts, and<br />
associated basalts, are far-travelled slices of the Phoenix plate.<br />
Rocks from the probable trench-slope basin, formerly assigned<br />
to the younger Fossil Bluff Group fore-arc basin sequence, now<br />
appear to be part of a new, previously unrecognized formation.<br />
Hori, R. 1992. Radiolarian biostratigraphy at the<br />
Triassic/Jurassic Period boundary in bedded cherts from the<br />
Inuyama area, Central Japan. J. Geosci. Osaka City Univ.,<br />
35, 53-65.<br />
Vertical distributions of microfossils such as <strong>radiolaria</strong>ns and<br />
conodonts across the Triassic-Jurassic (T/J) boundary were clarified<br />
through the biostratigraphic study of two continuous sequences of<br />
bedded cherts in the Inuyama area, central Japan. Three types of<br />
taxons were recognized around the T/J boundary, 1) Upper Triassic<br />
type such as Squinabolella, 2) Upper Triassic-Lower Jurassic type<br />
such as Canoptum, and 3) Transition type (possibly earliest Jurassic<br />
type) such as Parahsuum and Bipedis. The <strong>radiolaria</strong>n fossils<br />
- 81 -<br />
changed gradually, not drastically, from Triassic type into Jurassic<br />
ones during the interval (ca. 7 m.y.) from the extinction of<br />
conodonts to the first appearance of a species of Bagotum.<br />
Ishida, K., Hashimoto, H. & Kozai, T. 1992. Lithoand<br />
bio-stratigraphy of the lower Cretaceous Hanoura<br />
formation in East Shikoku. Part 1. Hiura and Tsukigatani<br />
routes in Katsuuragawa area. J. Sci., Univ. Tokushima, 26, 1-<br />
57. (in Japanese)<br />
Ishida, K., Yamashita, M. & Ishiga, H. 1992. P/T<br />
boundary in pelagic sediments in the Tanba Belt, southwest<br />
Japan. Geol. Rep. Shimane Univ., 11, 39-57. (in Japanese)<br />
Ishiga, H. 1992. Middle Paleozoic <strong>radiolaria</strong>ns of the<br />
genus Ceratoikiscum from Japan. In: Centenary of Japanese<br />
Micropaleontology. (Ishizaki, K. & Saiti, T., Eds.). Terra<br />
Scientific Publishing Company, Tokyo. pp. 389-397.<br />
Iwata, K., Akamatsu, M. & Hirama, M. 1992.<br />
Radiolarian fossils from the pre-Tertiary chert in the Tonin-<br />
Aniva Peninsula, Sakhalin Island. Mem. hist. Mus.<br />
Hokkaido, 31, 11-16. (in Japanese)<br />
Iwata, K. & Tajika, J. 1992. Early Paleogene<br />
<strong>radiolaria</strong>ns from green and red mudstones in the Yubetsu<br />
Group and reconsideration of the age of their sedimentation.<br />
Rep. geol. Surv. Hokkaido, 63, 23-31.<br />
Reexamination of the <strong>radiolaria</strong>n fossils included in the red and<br />
green mudstones of the Yubetsu Group in the northeast Hokkaido<br />
was carried out. As the results, the red and green mudstones of the<br />
Toyosato Formation and the red siliceous shales of the Asahino<br />
Formation indicate early early Paleocene, and green mudstones of<br />
the Asahino Formation indicate late early Paleocene.<br />
Iwata, K., Watanabe, Y. & Tajika, J. 1992.<br />
Radiolarian biostratigraphic study of the Hakobuchi Group in<br />
the Nakatonbetsu area, north Hokkaido. Rep. geol. Surv.<br />
Hokkaido, 63, 1-21.<br />
Radiolarian biostratigraphic study of the Hakobuchi Group and<br />
the Upper Yezo Group in the Nakatonbetsu area, north Hokkaido, was<br />
carried out to establish <strong>radiolaria</strong>n zones of the uppermost<br />
Cretaceous System in northern Japan. We have provisionally<br />
recognized the following two zones; Protoxiphotractus perplexus and<br />
Chlathrocyclas hyronia zones. The former and the latter indicate<br />
early to middle Campanian and middle Campanian to early<br />
Maastrichtian, respectively.<br />
Iwata, K., Yamada, G. & Hirama, M. 1992.<br />
Radiolarian fossils from chert boulders occurred in the eastern<br />
coast of the Urup Island, Kuril Arc. Mem. hist. Mus.<br />
Hokkaido, 31, 17-24. (in Japanese)<br />
Jones, G., De Wever, P. & Robertson, A.H.F.<br />
1992. Significance of <strong>radiolaria</strong>n age data to the Mesozoic<br />
tectonic and sedimentary evolution of the northern Pindos<br />
Mountains, Greece. Geol. Mag., 129/4, 385-400.<br />
Radiolarians were extracted from siliceous sediments of the<br />
northern Pindos Mountains. in an attempt to establish the chronology<br />
of tectonic and stratigraphic events related to the evolution of the<br />
Pindos ocean basin. Three separate phases of siliceous<br />
sedimentation were identified: (i) (mid-) late Triassic; (ii) mid-late<br />
Jurassic and (iii) mid-late Cretaceous. The first two phases are also<br />
known from the Pindos and Sub-Pelagonian zones of southern and<br />
central Greece, and elsewhere in the Dinarides and Hellenides.<br />
However, the occurrence of Cretaceous radiolarites in the west<br />
central Tethyan region is somewhat unusual. Field observations<br />
suggest that from the mid-late Triassic through to the mid Jurassic,<br />
radiolarites were deposited on volcanic basement, or were<br />
interbedded with sediments associated with the late<br />
rifting/spreading stages in the development of the Pindos ocean.<br />
Radiolarites of mid-late Jurassic age are commonly interbedded with<br />
clastic sediments of ophiolitic derivation. This coincides with a<br />
phase of significant compression within the Hellenides, which caused<br />
intra-oceanic deformation of the Pindos ophiolite. The ophiolite was<br />
subsequently emplaced onto the margin of the Pelagonian<br />
microcontinent in latest Jurassic time (Kimmeridgian-early<br />
Tithonian), as evidenced by transgressive marine carbonates.<br />
However, the Pindos basin survived in reduced form until the early<br />
Tertiary, allowing radiolarites to accumulate again within Cretaceous<br />
post-tectonic clastic sequences.
Bibliography - 1992 Radiolaria 14<br />
Kaminski, M.A., Baumgartner, P.O., Bown,<br />
P.R., Haig, D.W., McMinn, A., Moran, M.J.,<br />
Mutterlose, J. & Ogg, J.G. 1992.<br />
Magnetostratigraphic synthesis of Leg 123: sites 765 and<br />
766 (Argo Abyssal Plain and lower Exmouth Plateau). In:<br />
Proceedings of the Ocean Drilling Program, Scientific<br />
Results. (Gradstein, F.M., Ludden, J.N. et al., Eds.), vol.<br />
123. College Station, TX (Ocean Drilling Program), pp.<br />
717-737.<br />
During ODP Leg 123, Sites 765 and 766 were drilled to<br />
examine the tectonic evolution, sedimentary history, and<br />
paleoceanography of the Argo Abyssal Plain and lower Exmouth<br />
Plateau. At each site, the quality of magnetostratigraphic and<br />
biostratigraphic records varies because of complicating factors,<br />
such as the predominance of turbidites, the presence of condensed<br />
horizons, or deposition beneath the CCD.<br />
Based primarily on the presence of nannofossils, the base of<br />
the sedimentary section at Site 765 was dated as Tithonian. A<br />
complete Cretaceous sequence was recovered at this site, although<br />
the sedimentation rate varies markedly through the section. The<br />
Cretaceous/Tertiary boundary is represented by a condensed<br />
horizon. The condensed Cenozoic sequence at Site 765 extends<br />
from the upper Paleocene to the lower Miocene. A dramatic increase<br />
in sedimentation rate was observed in the lower Miocene, and a 480m-thick<br />
Neogene section is present. The Neogene section is<br />
continuous, except for a minor hiatus in the lower Pliocene.<br />
The base of the sedimentary section at Site 766 is Valanginian,<br />
in agreement with the site's position on marine magnetic anomaly<br />
M11. Valanginian to Barremian sediments are terrigenous, with<br />
variable preservation of microfossils, and younger sediments are<br />
pelagic, with abundant well-preserved microfossils. Sedimentation<br />
rate is highest in the Lower Cretaceous and decreases continually<br />
upsection. Upper Cenozoic sediments are condensed, with several<br />
hiatuses.<br />
Kanamatsu, T., Nanayama, F., Iwata, K. &<br />
Fujiwara, Y. 1992. Pre-Tertiary systems on the western<br />
side of the Abashiri tectonic line in the Shiranuka area,<br />
eastern Hokkaido, Japan: Implications to the tectonic<br />
relationship between the Nemuro and Tokoro Belts. J. geol.<br />
Soc. Japan, 98/12, 1113-1128. (in Japanese)<br />
Kemkin, I.V., Rudenko, V.S. & Kojima, S. 1992.<br />
Early Cretaceous Radiolarians from the Chernaya River Area,<br />
Southern Sikhote-Alin. Bull. Nagoya Univ. Furukawa Mus.,<br />
8, 27-35.<br />
Early Cretaceous (Valanginian-Barremian) <strong>radiolaria</strong>n<br />
assemblages from clastic rocks (olistostrome-turbidite) distributed<br />
in the Chernaya River area indicate that the sedimentary rocks<br />
attributed to the Upper Paleozoic form an accretionary complex<br />
together with the rocks in the Dalnegorsk and Kavalerovo areas in<br />
the Taukha terrane to the north. Sedimentary rocks in the studied<br />
area include Permo-Carboniferous fusulinid-bearing limestone<br />
closely associated with basic volcanic rocks, Late Permian and Late<br />
Jurassic bedded chert with <strong>radiolaria</strong>ns, and shallow-marine clastic<br />
deposits with Berriasian-Valanginian fauna and flora. These rocks<br />
are all interpreted as blocks and slabs intermingled with the Early<br />
Cretaceous olistostrome and turbidite complexes formed during the<br />
subduction process along the continental margin of Northeast Asia<br />
Kiessling, W. 1992. Paleontological and facial features of<br />
the Upper Jurassic Hochstegen Marble (Tauern Window,<br />
Eastern Alps). Terra Nova, 4/2, 184-197.<br />
Micropalaeontological, microscopic and mineralogical<br />
investigations of the ductily deformed and greenschist-facies<br />
metamorphic Hochstegen Marble in the Tauern Window shed new<br />
light on its stratigraphy and facies.<br />
New <strong>radiolaria</strong>n and sponge spicule discoveries have been made<br />
in cherty limestone marbles. They confirm previous age assignments<br />
and permit for the first time a more exact micropalaeontological age<br />
determination of early Tithonian for the upper parts of the marble.<br />
Forty morphotypes of <strong>radiolaria</strong>ns could be distinguished; in one<br />
sample a Fisher diversity index of 6 is reached indicating deeper<br />
marine conditions. The spicule fauna is also diverse and shows<br />
affinity to the S-German Malm. In respect to all the data it can be<br />
presumed that carbonate sedimentation of the Hochstegen Marble<br />
took place in a deeper marine environment at the southern margin of<br />
the European continent (Helvetic realm) during the whole Late<br />
Jurassic.<br />
Kiminami, K., Niida, K., Ando, H., Kito, N.,<br />
Iwata, K., Miyashita, S., Tajika, J. &<br />
- 82 -<br />
Sakakibara, M. 1992. Cretaceous-Paleogene arc-trench<br />
systems in Hokkaido. In: Paleozoic and Mesozoic Terranes:<br />
Basement of the Japanese Island Arcs. 29th IGC Field Trip<br />
Guide Book. (Adachi, M. & Suzuki, K., Eds.), vol. 1. Nagoya<br />
University, Nagoya, Japan. pp. 1-43.<br />
Kimura, G., Rodzhestvenskiy, V.S., Okamura,<br />
K., Melinkov, O. & Okamura, M. 1992. Mode of<br />
mixture of oceanic fragments and terrigenous trench fill in an<br />
accretionary complex; example from southern Sakhalin.<br />
Tectonophysics, 202/2-4, 361-374.<br />
Four modes of mixture of oceanic materials such as cherts,<br />
limestones and basalts, and terrigenous trench fill sediments are<br />
recognized in the Cretaceous accretionary complexes in southern<br />
Sakhalin, Far eastern Pacific margin of the U.S.S.R. The first mode is<br />
a thin-skinned stacking of pelagic bedded cherts with black shale,<br />
due to duplex formation in association with shallow underplating or<br />
off-scraping. The second mode is a mixture of the uppermost part of<br />
the oceanic crust with terrigenous trench fill sediments due to<br />
olistostrome formation.<br />
Reconstruction of the original sequence in ascending order<br />
suggests that the basement is pillow basalt, with overlying pelagic<br />
sediments of chert and limestone, olistostrome caused by collapse<br />
of oceanic crust due to its bending before encountering a trench, and<br />
finally trenchfill sediments of turbidite. This sequence is imbricated<br />
by thrusting, which appears to have occurred at the time of<br />
underplating.<br />
The third mode is a tectonic mixing of oceanic fragments and<br />
terrigenous sediments due to shear which is related to<br />
underthrusting of the oceanic plate. A reduction in the supply of<br />
trench fill sediments causes copious accretion of the upper part of<br />
oceanic crust. The fourth mode is in-situ basalt volcanism at the<br />
trench, where thick baked margins of terrigenous shale are formed<br />
around the injected basalts. This mode appears to represent a ridgetrench<br />
encounter. These four different modes of mixing seem to be<br />
usual in ancient accretionary complexes in orogenic belts.<br />
Kito, N. & De Wever, P. 1992a. Nouvelles espèces<br />
d'Hagiastridae (radiolaires) du Jurassique Moyen de sicile<br />
(Italie). Rev. Micropaléont., 35/2, 127-141.<br />
Three new species of Hagiastridae (Radiolaria) of Middle<br />
Jurassic from Sicily are described. The definitions of Hagiastridae<br />
RIEDEL, Hagiastrinae RIEDEL, Tritrabinae BAUMGARTNER, Tritrabs<br />
BAUMGARTNER and Angulobracchia BAUMGARTNER are modified.<br />
Angulobracchia is included in this family. The genus Cavabracchia is<br />
newly described.<br />
Kito, N. & De Wever, P. 1992b. Revision of the<br />
classification and phylogeny of Hagiastridae (Radiolaria). In:<br />
Proceedings of the Third Radiolarian Symposium. (Sakai, T.<br />
& Aita, Y., Eds.), vol. 8 . News of Osaka<br />
Micropaleontologists, special Volume, Osaka. pp. 67-76. (in<br />
Japanese)<br />
The phylogenetic relation and taxonomic nature of Hagiastrid<br />
genera are examined by cladistic method. Thirty species are<br />
analysed based on 16 sets of morphologic characters. A new<br />
terminology for the canal-beam system is proposed. The analysis<br />
indicates that Archaeohagiastrum, Archaeotriastrum, Tetraditryma<br />
and Angulobracchia are monophyletic, Tetratrabs are paraphyletic,<br />
and Tritrabs, Hagiastrum and Homoeoparonaella are polyphyletic.<br />
Subfamily Tritrabinae is closely related to Hagiastrinae rather than<br />
Tetraditryminae. A proposed phylogenetic tree based on morphologic<br />
analysis is generally concordant with stratigraphic records.<br />
Kurimoto, C. 1992. Discovery of Jurassic <strong>radiolaria</strong>ns<br />
from the Takashiroyama formation in the Sasayama district,<br />
Hyogo Prefecture, southwest Japan. J. geol. Soc. Japan,<br />
98/8, 787-790. (in Japanese)<br />
Kuwahara, K. 1992. Late Carboniferous to Early Permian<br />
<strong>radiolaria</strong>n assemblages from Miyagawa area, Mie Prefecture,<br />
Japan. In: Proceedings of the Third Radiolarian Symposium.<br />
(Sakai, T. & Aita, Y., Eds.), vol. 8 . News of Osaka<br />
Micropaleontologists, special Volume, Osaka. pp. 1-7. (in<br />
Japanese)<br />
Late Carboniferous to Early Permian <strong>radiolaria</strong>n assemblages<br />
were recognized from allochthonous chert blocks in the Chichibu<br />
Belt, Miyagawa area, Mie Prefecture, Japan. I distinguish three<br />
assemblages based on the genus Pseudoalbeillella. One of these<br />
<strong>radiolaria</strong>n assemblages include Pseudoalbeillella u-forma Group.
Radiolaria 14 Bibliography - 1992<br />
This P. u-forma Group shows a wide variation in its pseudo-abdominal<br />
morphology.<br />
Kuwahara, K. & Sakamoto, M. 1992. Late Permian<br />
Albaillella (Radiolaria) from a bedded chert section in the<br />
Gujo-hachiman area of the Mino Belt, central Japan:<br />
preliminary report on morphometry and cluster analysis. J.<br />
Geosci. Osaka City Univ., 35, 33-52.<br />
Eight species of Late Permian Albaillella (A. excelsa, A. flexa n.<br />
sp., A. Iauta n. sp., A. Ievis, A. sp. aff. A. Ievis, A. triangularis, A. sp.<br />
A, and A. sp. B) were recognized from <strong>radiolaria</strong>n assemblages in a<br />
bedded chert section in the Gujo-hachiman area of the Mino Belt,<br />
Central Japan. Quantitative features were measured for a total of<br />
1000 specimens representing eight species of Albaillella. Their<br />
morphometry indicates morphological distinctions among species.<br />
From their stratigraphic distribution and resemblance of shell forms,<br />
A. excelsa, A. flexa, A. Iauta, A. sp. A, and A. sp. B are considered to<br />
have closely phylogenic relations.<br />
Cluster analysis was attempted to well preserved specimens<br />
representing five species of Albaillella, in order to ascertain<br />
classification by visual inspection. Each clustered group generally<br />
corresponds to each species.<br />
Lazarus, D.B. 1992. Antarctic Neogene <strong>radiolaria</strong>ns from<br />
the Kerguelen Plateau, Legs 119 and 120. In: Proceedings of<br />
the Ocean Drilling Program, Scientific Results. (Wise,<br />
S.W.J., Schlich, R. et al., Eds.), vol. 120. College Station,<br />
TX (Ocean Drilling Program), pp. 785-809.<br />
Abundant, generally well-preserved <strong>radiolaria</strong>ns from Sites<br />
737, 744, 745, 746, 747, 748, and 751 were used in stratigraphic<br />
analysis of Neogene, and particularly middle Miocene to Holocene,<br />
Kerguelen Plateau sediments. The composite Kerguelen section is<br />
more complete than the Weddell Sea sections recovered by Leg 113,<br />
and the <strong>radiolaria</strong>ns are better preserved. Leg 113 <strong>radiolaria</strong>n<br />
zonations of Weddell Sea sites were applicable with only slight<br />
modification, and three new zones—Siphonosphaera vesuvius,<br />
Acrosphaera? Iabrata, and Amphymenium challengerae—are<br />
proposed for the latest Miocene. Geologic age estimates are given<br />
for all <strong>radiolaria</strong>n zones used. Major hiatuses affecting most sites<br />
were seen within the middle Miocene, in the latest Miocene, and<br />
latest Pliocene. Five new species are described: Acrosphaera?<br />
Iabrata, Acrosphaera? mercurius, Siphonosphaera vesuvius,<br />
Actinomma? magnifenestra, and Helotholus? haysi.<br />
Ling, H.Y. 1992. Radiolarians from the Sea of Japan: Leg<br />
128. In: Proceedings of the Ocean Drilling Program,<br />
Scientific Results. (Piscotto, K.A., Ingle, J.C., Von<br />
Breymann, M.T. et al., Eds.), vol. 127-128/1. College<br />
Station, TX (Ocean Drilling Program), pp. 225-236.<br />
The analysis of <strong>radiolaria</strong>ns from Japan Sea subsurface<br />
sediments recovered during Leg 128 of the Ocean Drilling Program<br />
reveals that a warm-water assemblage similar to that of the North<br />
Pacific was replaced by unique post-middle Miocene faunas probably<br />
as a result of the restriction of oceanographic circulation. The<br />
modern fauna was gradually established only in the Pleistocene. No<br />
attempt was made to establish the <strong>radiolaria</strong>n zonation because of<br />
low species diversity and the absence of generally recognized index<br />
forms in the North Pacific. In the diagenetically altered quartz<br />
section, however, a <strong>radiolaria</strong>n assemblage correlative to the middle<br />
Miocene Cyrtocapsella tetrapera Zone of western Honshu was<br />
identified from Hole 799B.<br />
Ling, H.Y. & Kobayashi, H. 1992. Geological<br />
significance of siliceous microfossils from Dogo, Oki<br />
Islands. In: Centenary of Japanese Micropaleontology.<br />
(Ishizaki, K. & Saito, T., Eds.). Terra Scientific Publishing<br />
Company, Tokyo, Japan. pp. 439-447.<br />
Marcucci-Passerini, M. & Gardin, S. 1992. The<br />
Fosso Cupo Formation (northern Latium, Italy): redefinition<br />
and new age data from <strong>radiolaria</strong>n and calcareous nannofossil<br />
biostratigraphy. Cretaceous Res., 13, 549-563.<br />
The "Varicoloured Manganiferous Shales", cropping out at<br />
Monti della Tolfa (northern Latium, Italy) constitute the stratigraphic<br />
substratum of the Upper Cretaceous Pietraforte Flysch in the Ligurid<br />
nappes of the Northern Apennines. These shales are here renamed<br />
the 'Fosso Cupo Formation'. A detailed study of <strong>radiolaria</strong>ns and<br />
calcareous nannofossils permits assignment of this formation to the<br />
Turonian-late Santonian interval. Previous data indicated an<br />
uncertain age ranging from Aptian/Albian to Late Cretaceous. A new<br />
<strong>radiolaria</strong>n subspecies, Crucella cachensis tolfaensis, is described.<br />
- 83 -<br />
Maruyama, T., Takemura, A. & Hiroo, I. 1992.<br />
Result from ODP Leg 120 (Kerguelen Plateau) - Special<br />
reference to diatom, <strong>radiolaria</strong>n and paleomagnetism. Earth<br />
Sci., J. Assoc. geol. Collab. Japan, extra, 6, 154-160. (in<br />
Japanese)<br />
Matsuoka, A. 1992a. Skeletal growth of a spongiose<br />
<strong>radiolaria</strong>n Dictyocoryne truncatum in laboratory culture.<br />
Mar. Micropaleontol., 19/4, 287-297.<br />
The stages of skeletal growth of the <strong>radiolaria</strong>n Dictyocoryne<br />
truncatum were observed using scanning electron and light<br />
microscopy. Four growth stages were recognized through<br />
comparison of laboratory-grown individuals with various sized<br />
skeletons which were collected by plankton tows near Barbados.<br />
Skeletal size is expressed as test height, which is the largest value<br />
among the three dimensions between a base line and arm apex of a<br />
triangular skeleton. The early stage (stage 1), with a maximum<br />
height of less than approximately 120 µm, is a uniformly spongiose,<br />
triangular skeleton lacking arms and a patagium. The next stage<br />
(stage 2) is a triangular skeleton with slightly concave sides of ca.<br />
120-200 µm size with three arms and a lace-like patagium. Further<br />
accretion of silica on the patagium conceals its lace-like structure,<br />
making a skeleton (stage3;ca.200-280 µm) with a more uniformly<br />
spongiose patagium. The mature stage (stage 4) with a maximum<br />
height more than ca. 280 µm is a triangular skeleton with convex<br />
sides, resulting from an outward growth of the patagium. Additional<br />
maturation produces an accretion of spongiose silica on the central<br />
part of the skeleton, forming a thickly biconvex skeleton in<br />
transverse section. One hundred and one individuals of D. truncatum<br />
were cultured in the laboratory at 28 ° C, 35‰ salinity and 165<br />
µE/m 2 /s light intensity, with maximum and mean longevity of 37 and<br />
6.4 days, respectively. The mean growth of 57 specimens which<br />
grew in the laboratory culture was 24.7 µm, with a maximum of 95<br />
µm. The initial size of cultured specimens ranged from 103 to 325<br />
µm, covering all of the four growth stages. Some specimens grew<br />
from one stage to the next stage changing skeletal morphology. The<br />
mean growth rate of four specimens which grew from stage 3 to 4 in<br />
laboratory culture was 5.4 µm/day (range 4.5-6.5 µm/day).<br />
Sporadic growth patterns exhibiting periods of rapid growth (15-20<br />
µm per day ) punctuated by intervals of little or no growth were<br />
observed in some cultured specimens. The sporadic growth may be<br />
related to a physiological rhythm of the organisms rather than<br />
environmental factors. The silica-depositing capacity is related<br />
largely to the vitality of the organisms. Discolored specimens and<br />
specimens with weakly extended axopodia showed no skeletal<br />
growth.<br />
Matsuoka, A. 1992b. Diversity of Jurassic Nassellarians<br />
in Japan. In: Proceedings of the Third Radiolarian<br />
Symposium. (Sakai, T. & Aita, Y., Eds.), vol. 8. News of<br />
Osaka Micropaleontologists, special Volume, Osaka. pp. 63-<br />
66. (in Japanese)<br />
Matsuoka, A. 1992c. Jurassic-Early Cretaceous tectonic<br />
evolution of the Southern Chichibu terrane, southwest Japan.<br />
In: Significance and application of Radiolaria to terrane<br />
analysis. (Aitchison, J.C. & Murchey, B.L., Eds.), vol.<br />
96/1-2. Special Issue: Palaeogeogr. Palaeoclimatol.<br />
Palaeoecol., Elsevier, Amsterdam. pp. 71-88.<br />
The Southern Chichibu terrane fringes the southern margin of<br />
the Jurassic-Early Cretaceous accretionary complex of southwest<br />
Japan. Two subterranes, the Togano subterrane in the north and<br />
Sambosan subterrane to the south, are recognized by examination of<br />
the common features of the terrane. They are juxtaposed throughout<br />
the terrane from western Kyushu to the Kanto Mountains a distance<br />
of over 1000 km. The geology of the Sakawa area, central Shikoku,<br />
is described in detail to show an example of the terrane. The geology<br />
around Tsukumi in eastern Kyushu and Okutama in the Kanto<br />
Mountains is introduced to emphasize the common features of this<br />
terrane.<br />
The Togano subterrane is composed of predominantly Triassic<br />
Jurassic chert clastic sequences associated with subordinate<br />
Jurassic olistostromal sequences and Upper Jurassic-Lower<br />
Cretaceous limestone-bearing clastic sequences. The chert-clastic<br />
sequences show an upward-coarsening sequence which reflects<br />
landward drift of the sea floor from a pelagic realm towards a trench.<br />
The olistostromal sequence contains abundant upper Paleozoic<br />
blocks. This subterrane is characterized by a south-vergent<br />
imbricate structure and south-younging polarity of the chert-clastic<br />
sequences.<br />
The Sambosan subterrane consists of mainly Upper Jurassic-<br />
Lower Cretaceous olistostromal sequences associated with Upper<br />
Jurassic Lower Cretaceous limestone-bearing clastic sequences. The<br />
olistostromal sequence includes abundant Triassic-Jurassic chert<br />
blocks and Triassic limestone blocks accompanied by greenstones.
Bibliography - 1992 Radiolaria 14<br />
The limestone-bearing clastic sequences of both subterranes are<br />
regarded as shelf or inner-trench slope sediments deposited on the<br />
chert clastic and olistostromal sequences.<br />
Two major stages of tectonic development are discriminated.<br />
The Togano subterrane was formed by successive offscrape<br />
accretion mainly during the Middle to Late Jurassic. The Sambosan<br />
subterrane was constructed by collision-accretion of seamounts<br />
mainly during the Late Jurassic to Early Cretaceous. The difference<br />
in the tectonic processes is considered to relate to topography of<br />
subducting oceanic plate; an oceanic plate with an abyssal plain for<br />
the Togano subterrane and an oceanic plate with seamounts for the<br />
Sambosan subterrane.<br />
Matsuoka, A. 1992d. Jurassic and Early Cretaceous<br />
<strong>radiolaria</strong>ns from Leg 129, Sites 800 and 801, western Pacific<br />
Ocean. In: Proceedings of the Ocean Drilling Program,<br />
Scientific Results. (Larson, R.L., Lancelot, Y. et al., Eds.), vol. 129.<br />
College Station, TX (Ocean Drilling Program). pp. 203-220.<br />
Rich <strong>radiolaria</strong>n faunas were obtained continuously from Middle<br />
Jurassic to Lower Cretaceous radiolarite sequences at Sites 800<br />
and 801, drilled during Ocean Drilling Program Leg 129 in the<br />
western Pacific. Occurrences of 90 taxa are presented in tables for<br />
these sites. Seven <strong>radiolaria</strong>n zones, Dibolachras tytthopora,<br />
Cecrops septemporatus, Pseudodictyomitra carpatica,<br />
Pseudodictyomitra primitiva, Cinguloturris carpatica, Stylocapsa(?)<br />
spiralis, and Tricolocapsa conexa in descending order, were<br />
recognized in this interval. The radiolarite sequences of Sites 800<br />
and 801 encompass approximately the Berriasian to Hauterivian (or<br />
to Barremian) and the Bathonian/Callovian to Valanginian ages,<br />
respectively. At Site 801, a hiatus of early Oxfordian was identified.<br />
Matsuoka, A. 1992e. Observation of <strong>radiolaria</strong>ns and their<br />
symbionts on discoidal spumellarida. Fossils, 53, 20-28. (in<br />
Japanese)<br />
Matsuoka, A. 1992f. Observation and growth record of<br />
living <strong>radiolaria</strong>ns - a case study of Dictyocoryne truncatum.<br />
Hyoseki: Tsurumatsu MANABE, memorial volume, 10, 67-<br />
76. (in Japanese)<br />
Matsuoka, A. & Anderson, O.R. 1992. Experimental<br />
and observational studies of <strong>radiolaria</strong>n physiological<br />
ecology: 5. Temperature and salinity tolerance of<br />
Dictyocoryne truncatum. Mar. Micropaleontol., 19/4, 299-<br />
313.<br />
The longevity and skeletal growth of Dictyocoryne truncatum,<br />
collected from surface waters near Barbados, were assessed in<br />
laboratory culture in relation to variations in temperature and<br />
salinity. The range of longevities for groups of organisms collected<br />
at different times, but maintained at 28 ° C and 35.0‰ salinity,<br />
exhibited a wide fluctuation ( 1-2 to 5-37 days). The amount of<br />
growth also showed a wide variation among the groups since it was<br />
generally proportional to the longevity. The causes of the variation in<br />
longevity and growth are not known, but we hypothesize that a<br />
combination of genetic variability and physical and biological factors<br />
intrinsic to the culture conditions produced the variability.<br />
D. truncatum showed a narrow temperature range for skeletal<br />
growth with an optimum in our culture conditions at about 28°C.<br />
Temperatures over 32°C or under 21°C suppressed skeletal growth.<br />
D. truncatum has a much wider temperature tolerance for survival<br />
than for growth. Longevity at temperatures as low as 15°C was<br />
comparable to that at 28°C. This indicates that D. truncatum can<br />
endure periods of relatively low temperatures. This may have<br />
survival advantage by conferring resistance to lower temperatures<br />
at great depths in the water column or during intrusion of colder<br />
water masses into warmer surface water regimes, but we have<br />
presently no evidence of their reproductive capacity at these lower<br />
temperatures. These results are consistent with a theory that D.<br />
truncatum is largely a surface-dwelling species surviving optimally<br />
in warmer water that supports optimum skeletal growth and<br />
maturation. The tolerance of cooler water, however, may also reflect<br />
biological adaptations related to variations in habitat during the<br />
reproductive cycle. Mature organisms may sink and release<br />
reproductive swarmers at greater depths in a water column, judging<br />
from the observation that mature individuals in culture withdrew<br />
their axopodia prior to swarmer release and settled to the bottom of<br />
culture vessels. The low temperature tolerance may also permit<br />
survival of juvenile organisms until they ascend into more warm<br />
surface water strata.<br />
Cultured D. truncatum has a wide growth and survival tolerance<br />
for variations in salinity. Mean growth and longevities were<br />
comparable at salinities of 27‰ and 35.0‰. A broad tolerance for<br />
variations in salinity can enhance survival at locations where wide<br />
- 84 -<br />
variations in salinity occur regularly as happens near Barbados<br />
where the surface water is diluted by river outflows. The low salinity<br />
tolerance is also consistent with the interpretation that D.<br />
truncatum dwells in near-surface water in low latitude, open ocean<br />
locations.<br />
Mizutani, S. & Kojima, S. 1992. Mesozoic <strong>radiolaria</strong>n<br />
biostratigraphy of Japan and collage tectonics along the<br />
eastern continental margin of Asia. In: Significance and<br />
application of Radiolaria to terrane analysis. (Aitchison, J.C.<br />
& Murchey, B.L., Eds.), vol. 96/1-2. Special Issue:<br />
Palaeogeogr. Palaeoclimatol. Palaeoecol., Elsevier,<br />
Amsterdam. pp. 3-22.<br />
Jurassic accretionary complexes mainly composed of<br />
Carboniferous to Permian limestone associated with greenstone,<br />
Triassic bedded chert, Jurassic siliceous shale and clastic rocks<br />
form the basement rocks of Japan. The stratigraphy of these<br />
complexes has recently been analysed utilizing <strong>radiolaria</strong>n fossils,<br />
resulting in the discovery that Japan comprises a collage of<br />
disrupted terranes. International co-operative works reveal that<br />
lithologically and biostratigraphically similar terranes are distributed<br />
in northeast China (Nadanhada terrane) and Sikhote-Alin, USSR<br />
(Khabarovsk terrane). Paleomagnetic studies demonstrate that prior<br />
to opening of the Sea of Japan the Japanese Islands were located<br />
much closer to the eastern margin of the Asian continent where the<br />
Nadanhada and Khaborovsk terranes are now exposed. Features of<br />
the Mino terrane in central Japan are characteristic of these<br />
terranes which originally formed along the continental margin of East<br />
Asia. Seamounts covered by fossiliferous limestone formed during<br />
the Carboniferous to Permian at low latitudes. The seamounts drifted<br />
towards a continental margin together with upper Paleozoic<br />
sediments, Triassic bedded chert and Lower Jurassic siliceous shale<br />
which accumulated around them. Upper Paleozoic, Triassic and Lower<br />
Jurassic formations were accreted to the eastern continental<br />
margin, which was a large tectonic collage developed as the Chinese<br />
mainland during the Late Triassic. Enormous amounts of clastic<br />
detritus were deposited in sedimentary basins where jumbling and<br />
telescoping of pelagic sediments took place in a complicated fashion<br />
producing a melange. The provenance of clastic detritus within the<br />
Mino terrane is interpreted as a platform on which Permian and<br />
Carboniferous calcareous sediments containing diagenetic lutecite<br />
and orthoquartzite formations were widespread. These formations<br />
covered a Precambrian metamorphic and granodioritic basement<br />
similar to that seen in the South China region. Accretion culminated<br />
in the earliest Cretaceous and the large disrupted terrane which had<br />
developed was transpressed north-wards along the eastern margin<br />
of the continent. During this period of dispersal the original terrane<br />
was sheared, fragmented and separated into many smaller terranes<br />
some of which were transported to the Sikhote-Alin region by the<br />
Late Cretaceous. The most recent dispersal occurred during the<br />
opening of the Sea of Japan, which is closely related to the latest<br />
movement of the Pacific plate.<br />
Studies of <strong>radiolaria</strong>n micropaleontology and the significance of<br />
these fossils to the resolution of the biostratigraphy and the<br />
tectonic history of Japan are reviewed. The results of<br />
biostratigraphic analyses are discussed in relation to the Mesozoic<br />
tectonics of East Asia.<br />
Molinie, A.J. & Ogg, J.G. 1992. Milankovitch cycles<br />
in Upper Jurassic-Lower Cretaceous radiolarites of the<br />
equatorial Pacific: spectral analysis and sedimentation rate<br />
curves. In: Proceedings of the Ocean Drilling Program,<br />
Scientific Results. (Larsen, R.L., Lancelot, Y. et al., Eds.),<br />
vol. 129. College Station, TX (Ocean Drilling Program), pp.<br />
529-547.<br />
Periodic changes in depositional environments due to<br />
Milankovitch astronomical climate cycles can cause cyclic patterns<br />
in sedimentation properties as recorded by logging data. Ocean<br />
Drilling Program Site 801 recovered Callovian (upper Middle<br />
Jurassic) through Valanginian (Lower Cretaceous) clayey<br />
radiolarites, originally deposited in a near-equatorial setting. Cycles<br />
of variable concentration of <strong>radiolaria</strong>ns and clay, and associated<br />
changes in degree of silicification were apparent in the geophysical<br />
logs, especially in the gamma-ray signal and the Formation<br />
MicroScanner. Three-dimensional spectral analysis was performed<br />
on the gamma-ray log signal using a 40-m sliding window. The<br />
dominant spectral peaks maintain the same relative ratios in<br />
frequency as the 413-k.y., 123-k.y., and 95-k.y. Milankovitch<br />
periods of eccentricity. The wave lengths of these eccentricitymodulated<br />
cycles were used to determine rates and discontinuities<br />
in sedimentation with depth.<br />
Two sharp discontinuities in sedimentation rate were inferred:<br />
(1) Callovian alternations of red radiolarite and claystone, with a<br />
sedimentation rate of approximately 14.5 m.y., is terminated by a<br />
Callovian/Oxfordian boundary hiatus, and the overlying upper<br />
Oxfordian through lowest Tithonian clay-rich radiolarites and the
Radiolaria 14 Bibliography - 1992<br />
lower Tithonian banded chert have an average sedimentation rate of<br />
7 m/m.y.: (2) a discontinuity of probable late Tithonian-early<br />
Berriasian age terminates the Tithonian banded chert; the overlying<br />
Berriasian through Valanginian radiolarite has a mean sedimentation<br />
rate of 11.5 m/m.y. These computed sedimentation rates and<br />
interpreted discontinuities are consistent with the stratigraphy of<br />
the recovered sediments and the uncertainties in the geological time<br />
scale.<br />
Eccentricity cycles identified in the gamma-ray signal were<br />
matched to corresponding features on the Formation MicroScanner<br />
high-resolution imagery of clay content and degree of silicification.<br />
Eccentricity cycles are manifested as groupings of beds of higher<br />
<strong>radiolaria</strong>n content and silicification. Milankovitch climate cycles<br />
may affect the intensity of equatorial Pacific upwelling, hence the<br />
surface productivity of <strong>radiolaria</strong>ns, and the amount of eolian dust<br />
and clay contributed to the sediments.<br />
Momoi, H., Ishida, K. & Yamasaki, T. 1992.<br />
Radiolarian geological ages of some host cherts of bedded<br />
manganese ore deposits in the Chichibu belt of Ehime<br />
Prefecture, Japan. Mem. Ehime Univ. nat. Sci., Ser. D (Earth<br />
Sci.), 1, 71-89. (in Japanese)<br />
Montgomery, H., Pessagno, E., Soegaard, K.,<br />
Smith, C., Muñoz, I. & Pessagno, J. 1992.<br />
Misconceptions concerning the Cretaceous/Tertiary boundary<br />
at the Brazos River, Falls County, Texas. Earth and planet.<br />
Sci. Lett., 109, 593-600.<br />
Detailed biostratigraphic analysis (planktonic foraminifera and<br />
nannofossils) of sixteen K/T (Cretaceous/Tertiary) boundary<br />
sections in and near the Brazos River, Falls County, Texas indicates<br />
that a lithologically distinctive, coarse clastic event bed previously<br />
attributed to a meteorite impact-generated tsunami at the end of the<br />
Cretaceous was actually deposited during the early Tertiary (Danian:<br />
K/T + at least 230,000 years). A tsunami origin for this event bed<br />
is doubtful, but if a bolide-splashdown tsunami did generate the<br />
event bed, this putative meteorite impact must have occurred well<br />
into the Danian during the post-extinction, faunal recovery phase<br />
having little effect on extant foraminiferal and coccolith populations.<br />
Montgomery, H., Pessagno, E.A.J. & Muñoz,<br />
I.M. 1992. Jurassic (Tithonian) Radiolaria from La Désirade<br />
(Lesser Antilles): preliminary paleontological and tectonic<br />
implications. Tectonics, 11/6, 1426-1432.<br />
Jurassic (upper Tithonian) Radiolaria recovered from bedded,<br />
red ribbon cherts on La Désirade, Guadeloupe, are the oldest fossils<br />
yet discovered in the Lesser Antilles. This age not only corroborates<br />
contested isotopic ages for the igneous basement of La Désirade but<br />
also demonstrates that previously reported differences in basement<br />
ages for the central and eastern end of the island are invalid. In<br />
addition, La Désirade chert yielded a higher-latitude, Northern<br />
Tethyan to Southern Boreal Realm <strong>radiolaria</strong>n assemblage (indicating<br />
deposition at a minimum of 22° north or south of the Jurassic<br />
paleoequator). Because Northern Tethyan or Boreal Jurassic oceanic<br />
crust did not exist in the spreading gap between North and South<br />
America, or east to Eurasia, we conclude that La Désirade oceanic<br />
crust formed in the Pacific. The fact that no Upper Jurassic red<br />
ribbon chert has been found in the Atlantic Ocean or in the Caribbean<br />
aside from in displaced oceanic fragments in Puerto Rico and the<br />
Dominican Republic lends additional support to a Pacific origin for<br />
the oldest crustal fragment in the Lesser Antilles.<br />
Mori, K., Okami, K. & Ehiro, M. 1992. Paleozoic<br />
and Mesozoic sequences in the Kitakami mountains. In:<br />
Paleozoic and Mesozoic Terranes: Basement of the Japanese<br />
Island Arcs. 29th IGC Field Trip Guide Book. (Adachi, M. &<br />
Suzuki, K., Eds.), vol. 1. Nagoya University, Nagoya,<br />
Japan. pp. 81-114.<br />
Motoyama, I. 1992. Neogene <strong>radiolaria</strong>n stratigraphy in<br />
the Tsugaru Peninsula, Aomori Prefecture, northern Japan. In:<br />
Proceedings of the Third Radiolarian Symposium. (Sakai, T.<br />
& Aita, Y., Eds.), vol. 8 . News of Osaka<br />
Micropaleontologists, special Volume, Osaka. pp. 89-100.<br />
(in Japanese)<br />
Radiolarians have been analyzed from an middle Miocene<br />
through Pliocene sequence of marine siliceous sediments exposed on<br />
the Tsugaru Peninsula, northernmost Honshu. The middle to upper<br />
Miocene diatomaceous mudstone contains well preserved siliceous<br />
microfossils. Six <strong>radiolaria</strong>n events were selected. Based on three of<br />
them, five <strong>radiolaria</strong>n zones were recognized: Eucyrtidium asanoi,<br />
Eucyrtidium inflatum, Lychnocanoma nipponica magnacornuta,<br />
"Anthocorys akitaensis" and Thecosphaera japonica. "A. akitaensis"<br />
- 85 -<br />
Zone is a new zone proposed for the middle upper Miocene. This<br />
<strong>radiolaria</strong>n stratigraphy was combined with the diatom stratigraphy<br />
proposed by AKIBA (1986). A brief comment was made on the late<br />
Miocene <strong>radiolaria</strong>n assembrage.<br />
Murchey, B.L. & Jones, D.L. 1992. A mid-Permian<br />
chert event: widespread deposition of biogenic siliceous<br />
sediments in coastal, island arc and oceanic basins. In:<br />
Significance and application of Radiolaria to terrane<br />
analysis. (Aitchison, J.C. & Murchey, B.L., Eds.), vol.<br />
96/1-2. Special Issue: Palaeogeogr. Palaeoclimatol.<br />
Palaeoecol., Elsevier, Amsterdam. pp. 161-174.<br />
Radiolarian and conodont correlations of Permian siliceous<br />
rocks from twenty-three areas in the circum-Pacific and<br />
Mediterranean regions reveal a widespread Permian Chert Event<br />
during the middle Leonardian to Wordian. Radiolarian- and (or)<br />
sponge spicule-rich siliceous sediments accumulated beneath high<br />
productivity zones in coastal, island arc and oceanic basins. Most of<br />
these deposits now crop out in fault-bounded accreted terranes.<br />
Biogenic siliceous sediments did not accumulate in terranes<br />
Iying beneath infertile waters including the marine sequences in<br />
terranes of northern and central Alaska. The Permian Chert Event is<br />
coeval with major phosphorite deposition along the western margin<br />
of Pangea (Phosphoria Formation and related deposits).<br />
A well-known analogue for this event is middle Miocene<br />
deposition of biogenic siliceous sediments beneath high productivity<br />
zones in many parts of the Pacific and concurrent deposition of<br />
phosphatic as well as siliceous sediments in basins along the coast<br />
of California. Interrelated factors associated with both the Miocene<br />
and Permian depositional events include plate reorientations, small<br />
sea-level rises and cool polar waters.<br />
Murray, R.W., Jones, D.L. & Buchholtz-ten-<br />
Brink, M.R. 1992. Diagenetic formation of bedded chert:<br />
Evidence from chemistry of the chert-shale couplet. Geology,<br />
20/3, 271-274.<br />
Theories concerning the formation of bedded chert traditionally<br />
have emphasized either depositional or diagenetic processes. Major<br />
and rare earth element data from Franciscan assemblage (Mesozoic)<br />
and Claremont Formation (Miocene) bedded chert sequences, along<br />
with physical observations such as the presence of rare and highly<br />
corroded <strong>radiolaria</strong>ns in shale interbeds, are most consistent with a<br />
dominantly diagenetic origin of chert-shale couplets and are<br />
incompatible with many depositional theories. Chemical distributions<br />
between Franciscan and Claremont bedded chert-shale closely<br />
match chemical fractionations recorded by Monterey Formation and<br />
Deep Sea Drilling Project-sampled cherts formed by diagenetic SiO 2<br />
dissolution, transport and reprecipitation, suggesting that diagenetic<br />
migration of SiO 2 from proto-shale to proto-chert is also largely<br />
responsible for chert-shale couplets. Identical Ce anomalies<br />
(Ce/Ce*) found in immediately adjacent chert-shale layers indicate<br />
that turbidites or other transport mechanisms are not responsible<br />
for the alternating beds. Neither the chemistry of the chert-shale<br />
couplet nor the overall stratigraphy of the sequences is consistent<br />
with couplet formation being caused by productivity fluctuations.<br />
Chemical mass balance calculations reconstructing the total bulk<br />
sediment composition suggest that modern siliceous sequences do<br />
not contain enough labile biogenic SiO 2 to form entire stratigraphies<br />
of bedded chert.<br />
Musashino, M., Imoto, N., Shimizu, D. &<br />
Ishiga, H. 1992. Mesozoic accreted terranes of<br />
northwestern Kyoto. In: Paleozoic and Mesozoic Terranes:<br />
Basement of the Japanese Island Arcs. 29th IGC Field Trip<br />
Guide Book. (Adachi, M. & Suzuki, K., Eds.), vol. 1. Nagoya<br />
University, Nagoya, Japan. pp. 205-212.<br />
Nagai, H. & Mizutani, S. 1992. Jurassic (Bathonian)<br />
<strong>radiolaria</strong>ns from the Snowshoe Formation, east-central<br />
Oregon, North America. In: Proceedings of the Third<br />
Radiolarian Symposium. (Sakai, T. & Aita, Y., Eds.), vol. 8.<br />
News of Osaka Micropaleontologists, special Volume,<br />
Osaka. pp. 47-61. (in Japanese)<br />
We examined <strong>radiolaria</strong>n fossils in the upper part of the<br />
Snowshoe Formation of Oregon. Their geological age is assigned by<br />
ammonite biostratigraphy to be late Bathonian. Eucyrtidiellum<br />
pustulatum and Pantanellium foveatum, both being common in the<br />
Japanese Jurassic formations, are found in the upper Bathonian part<br />
of the Snowshoe Formation. On the basis of the concurrent<br />
occurrence of these species and the evolutional trend of<br />
Eucyrtidiellum as well, we reached the following conclusion: the<br />
Japanese Upper Bathonian stage is located in a formation younger<br />
than the Unuma echinatus assemblage zone and older than, or in the
Bibliography - 1992 Radiolaria 14<br />
older part of, the Dictyomitrella(?) kamoensis-Pantanellium<br />
foveatum assemblage zone.<br />
Nagai, H. & Zhu, S. 1992. Permian Radiolaria from the<br />
Gufeng formation of Anhui Province and the Dalong<br />
formation of the Nanjing Area, China. Bull. Nagoya Univ.<br />
Furukawa Mus., 8, 1-11.<br />
Permian <strong>radiolaria</strong>ns were extracted from chert samples<br />
collected in the Gufeng Formation of Anhui Province and the Dalong<br />
Formation of the Nanjing area in China. The <strong>radiolaria</strong>n assemblage in<br />
the former sample includes abundant Pseudoalbaillella fusiformis<br />
Holdsworth and Jones, assignable to the Middle Permian, The latter<br />
one includes Hegleria ? sp., Octatormentum ? sp., Pseudoalbaillella<br />
sp. aff. P. longicornis Ishiga and Imoto, and Latentifistula sp cf. L<br />
patagilaterala Nazarov and Ormiston, and they are Late Permian in<br />
age.<br />
Nanayama, F. 1992. Stratigraphy and facies of the<br />
Paleocene Nakanogawa Group in the southern part of central<br />
Hokkaido, Japan. J. geol. Soc. Japan, 98/11, 1041-1059.<br />
(in Japanese)<br />
Nigrini, C. & Caulet, J.P. 1992. Late Neogene<br />
<strong>radiolaria</strong>n assemblages characteristic of Indo-Pacific areas of<br />
upwelling. Micropaleontology, 38/2, 139-164.<br />
Comparison of <strong>radiolaria</strong>n faunas in Late Neogene sediments<br />
from the Peru margin, the Oman margin and from beneath the<br />
Somalian gyres allowed definition of an assemblage characteristic of<br />
areas of upwelling. We describe the stratigraphic and geographic<br />
ranges of 12 previously studied and 10 new or newly described taxa.<br />
These forms fall into 3 categories: (1) endemic upwelling (14<br />
species); (2) displaced temperate (3 species); and (3) enhanced<br />
tropical (5 species). Not all elements of the assemblage are present,<br />
or in like abundances, in each upwelling area studied, but there is<br />
sufficient matching to allow identification of the assemblage. Eight<br />
long ranging species exhibit diachronous first appearances up to 7<br />
my older in the Oman material than in the Peru material.<br />
Nishimura, A. 1992. Paleocene <strong>radiolaria</strong>n<br />
biostratigraphy in the northwest Atlantic at Site 384, Leg 43,<br />
of the Deep Sea Drilling Project. Micropaleontology, 38/4,<br />
317-362.<br />
Two zones, Bekoma campechensis and B. bidartensis Zones,<br />
were recognized and three new subzones, Peritiviator (?) dumitricai,<br />
Orbula discipulus and Stylotrochus nitidus-Pterocodon (?) poculum<br />
Subzones are newly defined based on the Paleocene samples from<br />
DSDP Site 384. A new genus and 35 new taxa are described herein.<br />
Nishimura, A.A. & Ikehara, K. 1992. Deep-Sea<br />
sediments in the southern part of the central Pacific basin<br />
(GH82-4 area). Geol. Surv. Japan, Cruise Rep., 22, 85-96.<br />
(in Japanese)<br />
During the GH82-4 Cruise, areal distribution of sediments and<br />
sedimentary history were studied in the south of the Nova-Canton<br />
Trough, central Equatorial Pacific (Fig. VI-1) in relation to the<br />
genesis of manganese nodules. A small area was selected for smallscale<br />
sampling in the eastern margin of the whole survey area (Fig.<br />
VI-2). Sampling methods of sediments and manganese nodules are<br />
as follows; double spades box corer (15 sites), piston corer (20<br />
sites), and free-fall grab with a small sediment sampler (39 sites).<br />
Box and piston core sites are shown in Tables VI-1 and Vl-2 and in<br />
Figures VI-I and VI-2. Sediments collected by a box corer, piston<br />
corer, and free-fall grab sampler were treated in the same manner as<br />
in previous works (Nishimura, 1984 and 1986). Sediment lithology<br />
was classified according to the compositions of sediments<br />
determined on smear slides under a microscope. The framework of<br />
sediment classification is shown in Table VI-3. Age estimation of the<br />
core sequences are based on preliminary micropaleontologic<br />
analysis and a study of remnant magnetism of sediments (Yamazaki,<br />
chapter Vll of this volume). This chapter describes lithology of<br />
sediments and discusses sedimentary history concerning surface<br />
sediments and core sequences.<br />
Noble, P. 1992. Biostratigraphy of the Caballos<br />
Novaculaite-Tesnus Formation boundary, Marathon Basin,<br />
Texas. In: Significance and application of Radiolaria to<br />
terrane analysis. (Aitchison, J.C. & Murchey, B.L., Eds.),<br />
vol. 96/1-2. Special Issue: Palaeogeogr. Palaeoclimatol.<br />
Palaeoecol., Elsevier, Amsterdam. pp. 141-153.<br />
The Caballos Novaculite is a <strong>radiolaria</strong>n/sponge spicule chert<br />
and siliceous mudstone which represents the final episode of a 200<br />
- 86 -<br />
Ma span of dominantly biogenous hemipelagic sedimentation in<br />
Marathon Basin. It is overlain by the Tesnus Formation, an upwardcoarsening<br />
flysch sequence produced during the Ouachita Orogeny<br />
by the collision of Laurasia and Gondwana. Detailed <strong>radiolaria</strong>n<br />
biostratigraphy of the boundary between these two units has<br />
provided greater age control as to the onset of flysch deposition and<br />
provides a greater understanding of the sedimentary patterns<br />
produced in Ouachita basinal facies when switching modes of<br />
sedimentation from a passive to an active regime. Radiolarians and<br />
conodonts recovered from this interval show a hiatus equivalent to<br />
much of the Early Mississippian occurring in the vicinity of the<br />
boundary between the Caballos and Tesnus formations. In three<br />
sections, Late Mississippian (Meramecian) <strong>radiolaria</strong>ns overlie<br />
earliest Mississippian (early Kinderhookian) <strong>radiolaria</strong>ns in an<br />
apparently conformable sequence of siliceous shale. In a fourth<br />
section, Meramecian <strong>radiolaria</strong>ns overlie Late Devonian (Famennian)<br />
<strong>radiolaria</strong>ns and conodonts, separated by a conglomerate layer.<br />
These data indicate that a hiatus equivalent to the late<br />
Kinderhookian to Osagean time period is present and that local<br />
erosion into the Famennian part of the section occurred.<br />
Lithostratigraphically, this hiatus is coincident with the<br />
Caballos Novaculite-Tesnus Formation boundary in the central part<br />
of the basin, while at the western margin, it occurs 8 m above the<br />
base of the Tesnus Formation, immediately above a clastic zone<br />
containing olistoliths. Results from this investigation show that<br />
localized deposition of olistoliths occurred in the western basin<br />
margin during the Famennian (Late Devonian), followed by an interval<br />
of non-deposition in the Early Mississippian. Finally, basin-wide<br />
flysch deposition began in the Meramecian.<br />
Ogawa, Y., Ashi, J. & Fujioka, K. 1992. Vein<br />
structures and their tectonic implications for the development<br />
of the Izu-Bonin forearc, Leg 126. In: Proceedings of the<br />
Ocean Drilling Program, Scientific Results. (Taylor, B.,<br />
Fujioka, K. et al., Eds.), vol. 126. College Station, TX<br />
(Ocean Drilling Program), pp. 195-207.<br />
Samples with vein structures were taken from Sites 787 and<br />
793 in the forearc basin of the Izu-Bonin island arc off Aoga Shima<br />
and Sumisu Jima, respectively, between the present volcanic front<br />
and me outer arc high. The samples were studied by thin section, Xray<br />
radiograph, and magnetometer; they are discussed with respect<br />
to the tectonic implication of the vein structures to the island-arc<br />
development. Vein structures are developed in finer, more clayey,<br />
preferentially <strong>radiolaria</strong>n-bearing mudstone, subvertical to the<br />
bedding plane, which is mostly horizontal. The veins are restricted to<br />
certain horizons: in the upper Oligocene at Site 787 and in the lower<br />
Miocene at Site 793. The veins are filled with a dominant clay<br />
mineral (montmorillonite), which flowed into the vein when the<br />
fracture and concomitant stress drop occurred. Some clay mineral<br />
was deposited from the fluid that invaded the vein. Some veins might<br />
have occurred as hydraulic fractures. The shape, mode of<br />
occurrence, and other structural features indicate that the veins<br />
originated either as extension fractures or shear cleavages, and<br />
then were rotated by the following shearing parallel to the bedding.<br />
Sometimes the bedding-parallel slip planes are dislocated by the<br />
veins, and sometimes vice versa. This suggests that the vein<br />
formation and bedding parallel slip alternately occurred within the<br />
same stress environment. Vein attitude was measured by a<br />
magnetometer, after alternating field demagnetization; we interpret<br />
that they originally formed as subvertical planes, the trends of which<br />
average to N45W. The quantity of samples studied was small, but<br />
the trends suggest that the stress field for veining might have had a<br />
relative extensional stress axis mat lay subhorizontally and trended<br />
generally northeast. This stress orientation might be attributed to<br />
either bending or normal faulting in the forearc basin, at a time when<br />
the arc trended northwest.<br />
Ogawa, Y., Nishiyama, T., Obata, M., Nishi, T.,<br />
Miyazaki, K., Ikeda, T., Yoshimura, Y. &<br />
Nagakawa, K. 1992. Continental margin tectonics in<br />
Kyushu, southwest Japan- Mesozoic paired metamorphic<br />
belts and accretionary complexes. In: Paleozoic and<br />
Mesozoic Terranes: Basement of the Japanese Island Arcs.<br />
29th IGC Field Trip Guide Book. (Adachi, M. & Suzuki, K.,<br />
Eds.), vol. 1. Nagoya University, Nagoya, Japan. pp. 261-<br />
315.<br />
Ogg, J.G., Karl, S.M. & Behl, R.J. 1992. Jurassic<br />
through Early Cretaceous sedimentation history of the central<br />
equatorial Pacific and of Sites 800 and 801. In: Proceedings of<br />
the Ocean Drilling Program, Scientific Results. (Larsen, R.L.,<br />
Lancelot, Y. et al., Eds.), vol. 129. College Station, TX<br />
(Ocean Drilling Program), pp. 571-613.<br />
Sedimentation in the central Pacific during the Jurassic and<br />
Early Cretaceous was dominated by abundant biogenic silica. A
Radiolaria 14 Bibliography - 1992<br />
synthesis of the stratigraphy, lithology, petrology, and geochemistry<br />
of the radiolarites in Sites 801 and 800 documents the<br />
sedimentation processes and trends in the equatorial central Pacific<br />
from the Middle Jurassic through the Early Cretaceous. Paleolatitude<br />
and paleodepth reconstructions enable comparisons with previous<br />
DSDP sites and identification of the general patterns of<br />
sedimentation over a wide region of the Pacific.<br />
Clayey radiolarites dominated sedimentation on Pacific oceanic<br />
crust within tropical paleolatitudes from at least the latest<br />
Bathonian through Tithonian. Radiolarian productivity rose to a peak<br />
within 5° of the paleoequator. where accumulation rates of biogenic<br />
silica exceeded lOOOg/cm 2 /m.y. Wavy-bedded <strong>radiolaria</strong>n cherts<br />
developed in the upper Tithonian at Site 801 coinciding with the<br />
proximity of this site to the paleoequator. Ribbon-bedding of some<br />
<strong>radiolaria</strong>n cherts exposed on Pacific margins may have formed from<br />
silicification of radiolarite deposited near the equatorial highproductivity<br />
zone where <strong>radiolaria</strong>n/clay ratios were high.<br />
Silicification processes in sediments extensively mixed by<br />
bioturbation or enriched in clay or carbonate generally resulted in<br />
discontinuous bands or nodules of porcellanite or chert, e.g., a<br />
"knobby" radiolarite. Ribbon-bedded cherts require primary<br />
alternations of <strong>radiolaria</strong>n-rich and clay-rich layers as an initial<br />
structural template, coupled with abundant biogenic silica in both<br />
layers. During diagenesis, migration of silica from clay-rich layers<br />
leaves <strong>radiolaria</strong>n "ghosts" or voids, and the precipitation in<br />
adjacent radiolarite layers results in silicification of the inter<strong>radiolaria</strong>n<br />
matrix and infilling of <strong>radiolaria</strong>n tests. Alternations of<br />
claystone and clay-rich <strong>radiolaria</strong>n grainstone were deposited during<br />
the Callovian at Site 801 and during the Berriasian-Valanginian at<br />
Site 800, but did not silicify to form bedded chert.<br />
Carbonate was not preserved on the Pacific oceanic floor or<br />
spreading ridges during the Jurassic, perhaps due to an elevated<br />
level of dissolved carbon dioxide. During the Berriasian through<br />
Hauterivian, the carbonate compensation depth (CCD) descended to<br />
approximately 3500 m, permitting the accumulation of siliceous<br />
limestones at near-ridge sites. Carbonate accumuiation rates<br />
exceeded 1500 g/cm 2 /m.y. at sites above the CCD, yet there is no<br />
evidence of an equatorial carbonate bulge during the Early<br />
Cretaceous. In the Barremian and Aptian, the CCD rose, coincident<br />
with the onset of mid-plate volcanic activity.<br />
Abundance of Fe and Mn and the associated formation of<br />
authigenic Fe-smectite clays was a function of proximity to the<br />
spreading ridges, with secondary enrichments occurring during<br />
episodes of spreading-center reorganizations. Callovian radiolarite<br />
at Site 801 is anomalously depleted in Mn, which resulted either<br />
from inhibited precipitation of Mn-oxides by lower pH of interstitial<br />
waters induced by high dissolved oceanic CO2 levels or from<br />
diagenetic mobilization of Mn. Influx of terrigenous (eolian) clay<br />
apparently changed with paleolatitude and geological age.<br />
Cyclic variations in productivity of <strong>radiolaria</strong>ns and of<br />
nannofossils and in the influx of terrigenous clay are attributed to<br />
Milankovitch climatic cycles of precession (20,000 yr) and<br />
eccentricity ( 100,000 yr). Diagenetic redistribution of biogenic<br />
silica and carbonate enhanced the expression of this cyclic<br />
sedimentation.<br />
Jurassic and Lower Cretaceous sediments were deposited under<br />
oxygenated bottom-water conditions at all depths, accompanied by<br />
bioturbation and pervasive oxidation of organic carbon and metals.<br />
Despite the more "equable" climate conditions of the Mesozoic, the<br />
super-ocean of the Pacific experienced adequate deep-water<br />
circulation to prevent stagnation. Efficient nutrient recycling may<br />
have been a factor in the abundance of <strong>radiolaria</strong>ns in this ocean<br />
basin.<br />
Okamura, M. 1992. Cretaceous Radiolaria from Shikoku,<br />
Japan (Part 1). Mem. Fac. Sci., Kochi Univ., Series E<br />
(Geology), 13, 21-164.<br />
The biostratigraphic distribution of Early to Late Cretaceous<br />
<strong>radiolaria</strong>ns from eight sections in Shikoku, Japan, interpreted as<br />
belonging to any of the parts of the Cretaceous arc-trench system,<br />
is investigated and the stratigraphic range of each selected<br />
<strong>radiolaria</strong>n species is determined. Employing eight <strong>radiolaria</strong>n<br />
biohorizons set up on the base of the first and last occurrences of a<br />
given species, two sequences of upper Valanginian to Campanian<br />
strata are biostratigraphically divided into eight zones. These zones<br />
are, in ascending order: Acanthocircus dicranacanthos Zone,<br />
Sethocapsa uterculus Zone, Archaeodictyomitra lacrimula Zone,<br />
Pseudodictyomirta pseodomacrocephala morphotype C Zone,<br />
Holocryptocanium geysersensis Zone, Hemicryptocapsa polyhedra-<br />
Pyramispongia glascockensis Zone, Pseudoaulophacus pargueraensis<br />
Zone and Archaeospongoprunum salumi Zone.<br />
The Cretaceous Shikoku sequence among constructed through<br />
composite sequences at eight areas, which is correlated with the<br />
Yokonami chert and Shimantogawa turbidite, is attempted mainly by<br />
means of these datum levels and zonation herein proposed.<br />
- 87 -<br />
Correlation among intra-arc, fore-arc, trench and abyssal basin<br />
prove that <strong>radiolaria</strong>ns provide a valuable bases for constructing a<br />
biostratigraphic framework in the ancient arc-trench system.<br />
Additionary, comparisons of the proposed zonation with those of<br />
other fossil groups such as foraminifera, inocerami and ammonite<br />
from the Matsuyama, Monobe and Shimantogawa turbidite sequences<br />
provides important clues to the age assignment of the <strong>radiolaria</strong>n<br />
zones. Furthermore, Cretaceous oceanic plate stratigraphy is<br />
reconstructed based on chronology established by <strong>radiolaria</strong>n<br />
biostratigraphy.<br />
Osozawa, S. 1992. Double ridge subduction recorded in the<br />
Shimanto accretionary complex, Japan, and plate<br />
reconstruction. Geology, 20/10, 939-942.<br />
Combining a quantitative model relating ridge subduction and<br />
<strong>radiolaria</strong>n biostratigraphical data from the Shimanto belt including<br />
accreted midocean ridge basalt, the plate configuration for the<br />
western North Pacific since 83 Ma can be reconstructed. The Kula-<br />
North New Guinea and North New Guinea-Pacific ridges passed along<br />
the Japan arc. Assuming a constant plate motion, the half-spreading<br />
rates, angles at which ridges entered the trench, convergent rates<br />
and angles, and migration rates of triple junctions can be calculated.<br />
Otsuka, T., Kajima, M. & Hori, R. 1992. The<br />
Batinah Olistostrome of the Oman Mountains and Mesozoic<br />
<strong>radiolaria</strong>ns. In: Proceedings of the Third Radiolarian<br />
Symposium. (Sakai, T. & Aita, Y., Eds.), vol. 8. News of<br />
Osaka Micropaleontologists, special Volume, Osaka. pp. 21-<br />
34. (in Japanese)<br />
The Samail Ophiolite in the Oman Mountains is overlain by early<br />
Late Cretaceous supra-ophiolite sediments. The sediments are<br />
composed of the Suhaylah Formation, Zabyat Formation and Batinah<br />
Olistostrome in ascending order. The Batinah Olistostrome contains<br />
various size of olistoliths of serpentinite, basalt, limestone, chert<br />
and quartzite. Middle Triassic to early Late Cretaceous <strong>radiolaria</strong>ns<br />
are obtained mainly from chert olistoliths. Some olistoliths are<br />
correlated with the Samail Ophiolite and the Hawasina Series on the<br />
basis of their lithology and age. It is inferred that the Batinah<br />
Olistostrome was derived from the Samail and the Hawasina nappes<br />
in the west where they had formed a topographic high in the<br />
emplacement.<br />
Ozvoldová, L. 1992. The discovery of a Callovian<br />
<strong>radiolaria</strong>n association in the Upper Posidonia Beds of the<br />
Pieniny succession of the Klippen Belt (Western<br />
Carpathians). Geologica carpath., 43/2, 111-122.<br />
The first contribution dealing with the study of Middle Jurassic<br />
<strong>radiolaria</strong>ns in the Western Carpathians presents the composition of<br />
<strong>radiolaria</strong>n associations in the Upper Posidonia beds of the Pieniny<br />
succession (s.1.) in the Klippen Belt at Trstená in Orava. The<br />
assemblages have been assigned to the Lower to Middle Callovian.<br />
For comparison, the composition of an assemblage from the<br />
overlying radiolarite horizon of Upper Callovian to Upper Oxfordian<br />
age has been included.<br />
Ozvoldová, L. & Petercáková, M. 1992. Hauterivian<br />
<strong>radiolaria</strong>n association from the Luckovska Formation,<br />
Manin Unit (Mt. Butkov, western Carpathians). Geologica<br />
carpath., 43/5, 313-324.<br />
The paper deals with the occurrence of a rich <strong>radiolaria</strong>n<br />
microfauna in the limestones of the Lúckovská Formation of the<br />
Manín Unit (Mt. Butkov, Strázovské vrchy Mts., Central Western<br />
Carpathians). 36 taxa of <strong>radiolaria</strong>ns and four new species -<br />
?Acaeniotyle florea n. sp, Cyclastrum decorum n. sp, Orbiculiforma<br />
trispinosa n. sp. and Paronaella trifoliacea n. sp. have been identified<br />
in prospecting gallery St-02-38 m. The associations found represent<br />
the stratigraphical range of Uppermost Valanginian - Hauterivian.<br />
Findings of tintinnids and ammonites (Vasícek & Michalík 1986;<br />
Borza et al. 1987; Michalík et al. 1990) in this formation prove<br />
Barremian age. However, the calcareous microfauna and calcareous<br />
nannoplankton found in prospecting gallery St-02-38 m does not<br />
determine the exact age. The older age of <strong>radiolaria</strong>n associations<br />
can be explained here either by intraclasts of underlying rocks<br />
(Michalík et al. 1990) or by the assignation of the part of the<br />
Lúckovská Formation to Hauterivian in this prospecting gallery.<br />
Pessagno, E.A. & Mizutani, S. 1992. Radiolarian<br />
biozones of North America and Japan. In: The Jurassic of the<br />
Circum-Pacific. (Westerman, G.E.G., Eds.). Cambridge<br />
University Press, New York. pp. 293-295 and 578-585.<br />
The correlation chart presented herein (Figure 14.1) was<br />
compiled through a critical examination of published and unpublished
Bibliography - 1992 Radiolaria 14<br />
data for both Japan and North America. Because of the vast amount<br />
of unpublished data from both North America and Japan, it was first<br />
necessary for the authors to meet and to examine hundreds of<br />
scanning electron photomicrographs of North American and<br />
Japanese Radiolaria. Without such a meeting, any attempt at<br />
correlating North American and Japanese Jurassic <strong>radiolaria</strong>n<br />
biozones would have been, at best, an exercise in futility (plates 99-<br />
102). The <strong>radiolaria</strong>n zonation for North America followed herein<br />
represents an emended version of that presented by Pessagno et al.<br />
(1987b). The North American zonation shown in Figure 14.1 is the<br />
result of over 10 years of field and laboratory investigations by<br />
Pessagno and his associates. North American Jurassic samples were<br />
analyzed from Alaska, the Queen Charlotte Islands (British<br />
Columbia), east-central Oregon, California, Baja California Sur, and<br />
east-central Mexico. In establishing a zonal scheme for the North<br />
American Jurassic, Pessagno et al. (1987b) calibrated the<br />
<strong>radiolaria</strong>n biostratigraphy with those of the ammonites,<br />
calpionellids, Buchia, and other well-studied fossil groups. This<br />
amalgamation of data allowed a fit of the <strong>radiolaria</strong>n zonation to the<br />
ammonite-based chronostratigraphic scale. Figures showing the<br />
approximate correlation of <strong>radiolaria</strong>n zonal units with ammonite<br />
standard zones were presented by Pessagno et al. (1987b) and are<br />
not included here.<br />
Emendations to the original zonal scheme are minor. They<br />
include the introduction of a new subzone, Subzone 2 gamma, and<br />
the subsequent redefinition of Subzone 2 beta (Pessagno, Six, and<br />
Yang 1989). Subzone 2 gamma is defined from new data (Smith<br />
River Subterrane, Klamath Mountains, northwestern California)<br />
(Pessagno and Blome 1988, 1990) that document an interval of<br />
concurrence between the first appearance of Mirifusus Pessagno<br />
and the final appearance of Xiphostylus Haeckel ( primary marker<br />
taxa). The base of overlying Subzone 2 beta (Figure 14.1) is<br />
redefined to occur in the interval immediately above the final<br />
occurrence of Xiphostylus, whereas its top occurs immediately below<br />
the first occurrence of Parvicingula Pessagno s.s. Further discussion<br />
of the biostratigraphic, chronostratigraphic, and geochronological<br />
significance of Subzone 2 gamma is presented later.<br />
The Japanese <strong>radiolaria</strong>n zonation presented herein is that of<br />
Matsuoka and Yao (1986). This zonal scheme has become the<br />
standard for the western Pacific. Ammonites and other megafossils<br />
are very rare or totally absent from the Japanese <strong>radiolaria</strong>n-bearing<br />
succession (e.g., Mino terrane). Hence, the chronostratigraphic<br />
assignment of Japanese Jurassic <strong>radiolaria</strong>n biozones is based on<br />
North American data or data from elsewhere.<br />
Podobina, V.M. & Amon, E.O. 1992. Microfauna and<br />
biostratigraphy of Paleogene deposits of the Section<br />
"Sarbay" North-Western Turgay. In: Materials on<br />
Paleontology and Stratigraphy of the Western Siberia.<br />
(Podobina, V.M., Eds.). Tomsk Univ. Publisher, Tomsk. pp.<br />
88-96. (in Russian)<br />
Sakai, T. & Aita, Y. 1992. Proceedings of the Third<br />
Radiolarian Symposium. News of Osaka<br />
Micropaleontologists, special Volume, 8. Osaka, Japan.<br />
100 p.<br />
Sakai, T., Okada, H. & Aihara, A. 1992. Cretaceous<br />
and Tertiary active margin sedimentation: transect of Kyushu.<br />
In: Paleozoic and Mesozoic Terranes: Basement of the<br />
Japanese Island Arcs. 29th IGC Field Trip Guide Book.<br />
(Adachi, M. & Suzuki, K., Eds.), vol. 1. Nagoya University,<br />
Nagoya, Japan. pp. 317-354.<br />
Sancetta, C. 1992. Primary production in the glacial North<br />
Atlantic and North Pacific Oceans. Nature, 360/6401, 249-<br />
251.<br />
The conditions controlling primary production are very different<br />
in the modem North Atlantic and North Pacific oceans, a difference<br />
that is reflected in the composition of diatom fossils in surface<br />
sediments. By contrast, I report here evidence that during the last<br />
glacial interval the diatom assemblage, and by extrapolation the<br />
primary production, was very similar in the two regions. The modem<br />
analogues of these assemblages occur in sediments of Baffin Bay<br />
and the Sea of Okhotsk, both highly productive seas where ice is<br />
present. I infer that during the last glacial internal plankton biomass<br />
was at least as high as it is today in the North Atlantic, and was as<br />
much as an order of magnitude I higher in the North Pacific. I<br />
hypothesise that the presence of numerous icebergs, possibly<br />
associated with sea ice I supported high production of physical<br />
mechanisms (such as turbulent mixing and enhanced density<br />
stratification) and/or biogeochemical ones (such as supply of major<br />
or trace nutrients)<br />
- 88 -<br />
Sanfilippo, A. & Riedel, W.R. 1992. The origin and<br />
evolution of Pterocorythidae (Radiolaria): A Cenozoic<br />
phylogenetic study. Micropaleontology, 38/1, 1-36.<br />
A survey of pterocorythids throughout the Cenozoic shows that<br />
there are only two generalized, persistent stocks from which<br />
developed fourteen branches here treated as genera or subgenera.<br />
These branchings are the "speciations" of evolutionists, but we use<br />
the term "species" for chronospecies which would be subdivisions of<br />
the evolutionists anagenetic species. Thus we distribute the<br />
approximately fifty pterocorythid genera previously recognized<br />
among only sixteen genus-level taxa. We have found it necessary to<br />
describe the new genera Cryptocarpium and Albatrossidium, and the<br />
subgenera Calocyclior, Calocyclissima, Calocyclopsis, Podocyrtopsis<br />
and Podocyrtoges, as well as six new species to clarify generic<br />
origins and terminations.<br />
Cephalic structure tends to be conservative and distinctive at<br />
the generic level, as also does to a somewhat lesser extent the<br />
shape of the thorax and the nature of its wall and pores. More distal<br />
parts of the skeleton vary markedly within genera. Relationships can<br />
be determined only by following evolutionary changes through time in<br />
many cases, superficially similar species have quite different<br />
evolutionary origins.<br />
Sano, H., Wakita, K., Kojima, S. & Yamagata, T.<br />
1992. Late Mesozoic accretionary complex: Mino Terrane,<br />
Central Japan. In: Paleozoic and Mesozoic Terranes:<br />
Basement of the Japanese Island Arcs. 29th IGC Field Trip<br />
Guide Book. (Adachi, M. & Suzuki, K., Eds.), vol. 1. Nagoya<br />
University, Nagoya, Japan. pp. 197-203.<br />
Our field trip examines the stratigraphy, lithology, and<br />
structure of Paleozoic and Mesozoic rocks of the Mino terrane and<br />
intends to discuss its origin and tectonic evolution. The trip plans to<br />
meet rocks of the Mino terrane seven stops in the Neo-Miyama area,<br />
central Japan (Fig. 1). The Mino terrane is extensive in the<br />
continental side of Southwest Japan (Fig. 1). Its correlative terranes<br />
are described in northeast China and Sikhote-Alin (Kojima, 1989), in<br />
North Palawan, the Philippines (Isozaki et al., 1988), and on<br />
Ishigakijima Island at the southwestern extremity of Japan (Isozaki<br />
and Nishimura, 1989). The Mino terrane and its correlatives form a<br />
belt of Jurassic accretionary rocks fringing the western Pacific<br />
margin (Mizutani, 1987). The Mino terrane comprises a lithologically<br />
heterogeneous and structurally complicated aggregate of<br />
unmetamorphosed Paleozoic and Mesozoic rocks. Its major<br />
constituents are Permian basaltic rocks, carbonates, and chert,<br />
Triassic to Jurassic chert and related siliceous rocks, and Jurassic<br />
to lowest Lower Cretaceous sandstone and mudstone. The Jurassic<br />
terrigenous rocks are most extensive in the Mino terrane. These<br />
rocks are strongly deformed and form a series of fault-bounded,<br />
complexly stacked, originally southerly vergent, imbricated<br />
structural wedges. The complexly stacked wedges have been folded<br />
to form gentle synclines and anticlines on a mappable scale<br />
(Mizutani, 1964). The deformed rocks of the Mino terrane are<br />
unconformably covered by less deformed Late Cretaceous effusive<br />
rocks.<br />
Sano, H., Yamagata, T. & Horibo, K. 1992.<br />
Tectonostratigraphy of Mino terrane; Jurassic accretionary<br />
complex of southwest Japan. In: Significance and application<br />
of Radiolaria to terrane analysis. (Aitchison, J.C. &<br />
Murchey, B.L., Eds.), vol. 96/1-2. Special Issue:<br />
Palaeogeogr. Palaeoclimatol. Palaeoecol., Elsevier,<br />
Amsterdam. pp. 41-57.<br />
The Mino terrane, a disrupted accretionary terrane in central<br />
Japan, consists of four fault-bounded mappable units of Mesozoic<br />
and Paleozoic unmetamorphosed sedimentary rocks. The four units<br />
are described as (I) Permian greenstonecarbonate-chert unit, (2)<br />
Lower Triassic to lowest Cretaceous siliceous pelagite-distal<br />
turbidite unit, (3) Middle Jurassic proximal turbidite unit, and (4)<br />
upper Lower Jurassic to lowest Cretaceous olistostrome-slump unit.<br />
The first unit is interpreted as a sedimentary cover which was<br />
formed on and around a seamount in an open-ocean setting. The<br />
second unit records the accumulation of deep-water <strong>radiolaria</strong>n-rich<br />
sediments in a pelagic realm and a tapering wedge of trench<br />
turbidites. The third unit contains submarine fan sediments<br />
deposited in a possible trench-slope basin. The forth unit, labelled as<br />
sedimentary melange containing blocks derived from accretionary<br />
prisms, is considered to be submarine deposits which accumulated in<br />
a lower trench-slope basin to trench floor setting.<br />
An originally southward-vergent imbricate stacking of<br />
structural wedges of these four units characterizes the highly<br />
complicated structure of the Mino terrane rocks. Collision and<br />
subsequent offscraping accretion of Permian to Middle Jurassic<br />
oceanic rocks and Lower Jurassic to lowest Cretaceous clastic rocks<br />
provide the most satisfactory explanation for juxtaposition of the<br />
structural wedges of the four units which were originally laid down in
Radiolaria 14 Bibliography - 1992<br />
largely different depositional sites. These tectonic events most<br />
probably took place during Early Jurassic to Early Cretaceous time<br />
along an active continental margin of East Asia.<br />
Sarnthein, M., Pflaumann, U., Ross, R.,<br />
Tiedemann, R. & Winn, K. 1992. Transfer functions to<br />
reconstruct ocean paleoproductivity: a comparison. In:<br />
Upwelling Systems: Evolution Since the Early Miocene.<br />
(Summerhayes, C.P., Prell, W.L. & Emeis, K.C., Eds.), vol.<br />
64. Geological Society of London, special Publication,<br />
London, U. K. pp. 411-427.<br />
Oceanic plankton (export) productivity contributes to the<br />
control of glacial-to-interglacial changes in atmospheric CO2<br />
concentration. The extent of this contribution may be deciphered<br />
from global reconstruction of palaeoproductivity. We quantitatively<br />
estimate palaeoproductivity over the last 3500()0 years in the<br />
eastern equatorial Atlantic, using equations based on foraminiferal<br />
assemblages and marine organic carbon accumulation rates; and<br />
Make qualitative estimates using diatom and <strong>radiolaria</strong>n<br />
accumulation rates. These proxydata arc calibrated to data on<br />
modern primary production. When applied to the same set of marine<br />
sediment samples, the various reconstruction techniques produce<br />
productivity estimates with similar temporal productivity<br />
oscillations and a long term similar absolute productivity level,<br />
suggesting that each provides a good signal of productivity changes.<br />
Sashida, K. 1992a. Early Jurassic <strong>radiolaria</strong>ns from the<br />
Shomaru Pass-Higashiagano area, Hanno City, Saitama<br />
Prefecture, central Japan. In: Proceedings of the Third<br />
Radiolarian Symposium. (Sakai, T. & Aita, Y., Eds.), vol. 8.<br />
News of Osaka Micropaleontologists, special Volume,<br />
Osaka. pp. 35-46. (in Japanese)<br />
Three Early Jurassic <strong>radiolaria</strong>n assemblages are recognized in<br />
the Hanagiri Formation and the Nakato Formation (provisional name)<br />
distributed in the Shomaru Pass-Higashiagano area, Saitama<br />
Prefecture, central Japan. They are the Parahsuum simplum<br />
Assemblage, the Parahsuum takarazawaense Assemblage and the<br />
Laxtorum? jurassicum Assemblage, in ascending order. Based on<br />
stratigraphical and structural features and <strong>radiolaria</strong>n dating, the<br />
Hanagiri and Nakato Formations are correlative with the Middle<br />
Chichibu Belt (middle portion of the three folds Chichibu Belt) in the<br />
Outer Zone of Southwest Japan and are presumed to be products of<br />
the convergent complex of an oceanic plate during Early Jurassic<br />
time.<br />
Sashida, K. 1992b. Northern and middle Chichibu Belts of<br />
the Eastern Part of the Kanto Mountains, Central Japan. J.<br />
Geogr. (Tokyo), 101/7, 573-593. (in Japanese)<br />
Sashida, K. & Igo, H. 1992. Triassic <strong>radiolaria</strong>ns from a<br />
limestone exposed at Khao Chiak near Phatthalung, southern<br />
Thailand. Trans. Proc. palaeont. Soc. Japan, n. Ser., 168,<br />
1296-1310.<br />
We recovered well-preserved Triassic <strong>radiolaria</strong>ns from a thinbedded<br />
limestone exposed at Khao Chiak, near Phatthalung, southern<br />
Thailand. This <strong>radiolaria</strong>n fauna is associated with conodonts<br />
indicating a latest Spathian to earliest Anisian age and composed of<br />
families such as "Palaeozoic-type" Entactiniidae, Actinommidae,<br />
spicule-type Palaeoscenidiidae, and acanthodesmid Nassellaria. We<br />
propose a new genus and four new. species herein. The occurrence of<br />
the genera Entactinia Foreman and Polyentactinia Foreman is the<br />
first record from the Triassic.<br />
Shao, J.A., Tang, K.D., Wang, C.Y., Zang, Q.J.<br />
& Zhang, Y.P. 1992. Structural features and evolution of<br />
the Nadanhada terrane. Sci. China, Ser. B, 35/5, 621-630.<br />
The study of terranes has already become an important subject<br />
in research of the Circum-Pacific continental margin. This paper<br />
discusses proper understanding of the terrane conception and<br />
identifies existence of the Nadanhada terrane according to its<br />
difference from the neighbouring massifs in terms of evolutionary<br />
history, tectonic background, and deformation features, and to the<br />
fault-contact relation between them; analyzes the paleogeographic<br />
position variation of the Nadanhada terrane during the Triassic to<br />
late Jurassic and the period when the terrane was attached to the<br />
ancient continental marging; finally discusses the consequential<br />
effects of the terrane accretion from the observed tectonic events<br />
after terrane collage.<br />
Steiger, T. 1992. Systematik, stratigraphie und<br />
Palökologie der Radiolarien des Oberjura-Unterkreiden-<br />
- 89 -<br />
Grenzbereiches im Osterhorn-Tirolikum (Nördliche<br />
Kalkalpen, Salzburg und Bayern. Zitteliana, 19, 3-188.<br />
Upper Jurassic to Lower Cretaceous deposits of the Osterhorn<br />
Tyrolian Zone in the Northern Calcareous Alps (Austria) contain a<br />
rich <strong>radiolaria</strong>n fauna. Analysis of the organisms yielded 54 genera<br />
with 183 species. 9 genera and 30 species are new. The<br />
biostratigraphic sequence shows a good correlation with significant<br />
forms of the Tethys, particularly from the Late Tithonian through the<br />
Berriasian. The fauna is partly endemic and useful for a regional<br />
zonation. The morphologic examination showed a strong<br />
interdependence of morphotypes and sedimentary environment. In<br />
<strong>radiolaria</strong>n accumulations still missing elements of morphologic<br />
sequences within higher taxonomic categories (Actinommidae,<br />
Hagiastridae) were found. Transitional forms and supplementary<br />
structures of the tests indicate ontogenetic and reproductive<br />
stages. On the basis of a paleobathymetric model first clues for a<br />
<strong>radiolaria</strong>n depth zonation were recognized at the Jurassic—<br />
Cretaceous boundary interval.<br />
Sugiyama, K. 1992a. Lower and Middle Triassic<br />
<strong>radiolaria</strong>ns from Mt. Kinkazan, Gifu Prefecture, Central<br />
Japan. Trans. Proc. palaeont. Soc. Japan, n. Ser., 167,<br />
1180-1223.<br />
Well-preserved <strong>radiolaria</strong>ns have been obtained from the Lower<br />
and Middle Triassic in Mt. Kinkazan, Gifu City, Gifu Prefecture,<br />
central Japan. They are represented by three assemblages, namely<br />
the Parentactinia nakatsugawaensis assemblage (Spathian or older),<br />
Hozmadia gifuensis sp. nov. assemblage (early Anisian) and<br />
Triassocampe coronata assemblage (middle Anisian). On the basis of<br />
field observations, <strong>radiolaria</strong>n dating and some sedimentological<br />
examinations, the general stratigraphy in the studied area is<br />
tentatively reconstructed as a sequence of Lower Triassic black<br />
shale, siliceous shale to chert, and Middle Triassic bedded chert in<br />
ascending order. The occurrence of Permian <strong>radiolaria</strong>ns in the<br />
studied area is also discussed. Twenty-six species are newly<br />
described and four new genera are also proposed herein.<br />
Sugiyama, K. 1992b. Early Miocene <strong>radiolaria</strong>ns from the<br />
Toyohama formation, Morozaki Group, Aichi Prefecture,<br />
central Japan. J. geol. Soc. Japan, 98/1, 65-67. (in<br />
Japanese)<br />
Sugiyama, K. 1992c. Syscioscenium velamen gen. et sp.<br />
nov., a new sethoformid Radiolaria from the lower to middle<br />
Miocene of central Japan. Bull. Mizunami fossil Mus., Dr.<br />
Juinji Itoigawa, Mem. vol., 19, 215-218.<br />
Syscioscenium velamen gen. et sp. nov. is described from the<br />
Middle Miocene Oidawara Formation, Mizunami Group, and Lower<br />
Miocene Toyohama Formation, Morozaki Group. Although its bellshaped<br />
test is generally characteristic for some lophophaenids, this<br />
new species has a sethoformid skeletal structure.<br />
Sugiyama, K. 1992d. New spumellarians (Radiolaria) from<br />
the lower Miocene Toyohama formation, Morozaki Group,<br />
central Japan. Bull. Mizunami fossil Mus., Dr. Juinji<br />
Itoigawa, Mem. vol., 19, 193-197.<br />
Three spumellarians are newly described from decapod-bearing<br />
calcareous nodules embedded within the Lower Miocene Toyohama<br />
Formation, Morozaki Group, Aichi Prefecture. One new genus<br />
Enalomelon is also proposed herein.<br />
Sugiyama, K. & Furutani, H. 1992. Middle Miocene<br />
<strong>radiolaria</strong>ns from the Oidawara formation, Mizunami Group,<br />
Gifu Prefecture, central Japan. Bull. Mizunami fossil Mus.,<br />
Dr. Juinji Itoigawa, Mem. vol., 19, 199-213.<br />
The <strong>radiolaria</strong>ns are abundant microfossils through the Middle<br />
Miocene Oidawara Formation, Mizunami Group, Gifu Prefecture. In<br />
order to provide their fundamental information, this paper reports<br />
the occurrence of 47 characteristic <strong>radiolaria</strong>ns including four new<br />
species.<br />
Sugiyama, K., Nobuhara, T. & Inoue, K. 1992.<br />
Preliminary report on Pliocene <strong>radiolaria</strong>ns from the Nobori<br />
formation, Tonohama Group Shikoku, southwest Japan. J.<br />
Earth Sci. Nagoya Univ., 39, 1-30.<br />
99 taxa of <strong>radiolaria</strong>ns were discriminated from the type<br />
section of the Nobori Formation, Tonohama Group, Shikoku,<br />
Southwest Japan. The preliminary investigation has revealed that the<br />
type locality of the formation, also that of planktonic foraminifera<br />
Globorotalia tosaensis whose first appearance defines the base of<br />
the zone N21, is correlative with both the Sphaeropyle langii zone
Bibliography - 1992 Radiolaria 14<br />
(mid latitude) and the Spongaster pentas zone (low latitude) and that<br />
the age is middle to late Pliocene. The Nobori <strong>radiolaria</strong>n fauna is<br />
considered to be a transitional type from typical low to mid latitude<br />
fauna, and is characterized by the predominant occurrence of<br />
pyloniaceans, on the other hand, the nassellarians are relatively rich<br />
in Cycladophora pliocenica representing one of cold water species.<br />
Pseudodictyophimus hexaptesimus, Bathropyramis (?) pyrgina,<br />
Eucyrtidium lene are newly described.<br />
Swanberg, N.R. & Bjørklund, K.R. 1992. The<br />
<strong>radiolaria</strong>n fauna of western Norwegian fjords: a multivariate<br />
comparison of the sediment and plankton assemblages.<br />
Micropaleontology, 38/1, 57-74.<br />
Radiolarian assemblages from the plankton and sediments in<br />
various Norwegian fjords and sediments from stations in the<br />
Norwegian Sea were compared using multivariate analysis. The<br />
sediments were very different from all of the plankton in all seasons.<br />
This difference was the largest source of variability in the data set,<br />
followed in turn by differences due to season, regions, various<br />
fjords, depths and locale within a given fjord. The sediments did not<br />
average the seasonal plankton signals observed, but did conserve<br />
most of the geographical information presented in the plankton<br />
assemblage. The information in the plankton and sediments was<br />
conveyed by different groups of species. While the sediments can be<br />
excellent indicators of environmental conditions in the overlying<br />
water column, they say relatively little about the species<br />
composition in the overlying plankton.<br />
Swanberg, N.R. & Eide, L.K. 1992. The <strong>radiolaria</strong>n<br />
fauna at the ice edge in the Greenland Sea during summer,<br />
1988. J. marine Res., 50, 297-320.<br />
Radiolaria were sampled from the plankton at 18 stations<br />
during two cruises in the Greenland Sea during summer, 1988. A<br />
total of 43 species or categories of Radiolaria was found, but over<br />
90% of the <strong>radiolaria</strong>n fauna was dominated by adults or juveniles of<br />
4 species: the spumellarian, Actinomma leptodermum and the<br />
nassellaria, Amphimelissa setosa, Pseudodictyophimus gracilipes,<br />
and Peridium longispinum. The stations sampled ranged from icecovered<br />
areas high in nutrients to open water areas which were<br />
depleted in nutrients. These stations encompassed a gradient in the<br />
composition of the <strong>radiolaria</strong>n fauna from an assemblage dominated<br />
by juveniles and adults of A. setosa and P. gracilipes at the ice edge<br />
to one dominated by Actinomma juveniles, A. Ieptodermum, and P.<br />
Iongispinum in open water. The total abundance of Radiolaria<br />
correlated with integrated phaeopigment, but not with chlorophyll a.<br />
In discriminate function analysis the 'ice edge' <strong>radiolaria</strong>n species<br />
listed above correlated well with chlorophyll a and phaeopigments,<br />
while the 'open water' species did not. Several water masses occur in<br />
the area, which complicates the interpretation considerably, but the<br />
data are consistent with the development of a <strong>radiolaria</strong>n population<br />
in tempo with, and in all probability linked successionally to the<br />
development of the phytoplankton—microplankton bloom.<br />
Takahashi, O. & Ishii, A. 1992. Tectonostratigraphic<br />
division and <strong>radiolaria</strong>n biochronology of the Otaki Group of<br />
the northern Shimanto Belt, Kanto Mountains, central Japan<br />
- The deforming processes and duplex structures of the<br />
northern Shimanto Belt in the Kanto Mountains.<br />
Bull.Saitama Mus. nat. Hist., 10, 11-28.<br />
Takemura, A. 1992. Radiolarian Paleogene<br />
biostratigraphy in the southern Indian Ocean, Leg 120. In:<br />
Proceedings of the Ocean Drilling Program, Scientific<br />
Results. (Wise, S.W.J., Schlich, R. et al., Eds.), vol. 120.<br />
College Station, TX (Ocean Drilling Program), pp. 735-756.<br />
During Ocean Drilling Program Leg 120, an almost complete<br />
Paleogene sediment section on the Kerguelen Plateau in the southern<br />
Indian Ocean was recovered. The biostratigraphy of <strong>radiolaria</strong>ns from<br />
these sediments at Sites 748 and 749 is studied. A biostratigraphic<br />
framework established in low and middle latitudes is not applicable<br />
because of the absence of most zonal marker species. Biogenic opal<br />
is present only in middle Eocene to Oligocene sediments, and three<br />
new zones-Lychnocanoma conica, Axoprunum(?) irregularis, and<br />
Eucyrtidium spinosum zones-are proposed. The Paleogene antarctic<br />
<strong>radiolaria</strong>n fauna is different from that in low and middle latitudes.<br />
Three new species, Axoprunum(?) irregularis, Eucyrtidium cheni, and<br />
Eucyrtidium spinosum, are described.<br />
Taketani, Y. & Kanie, Y. 1992. Radiolarian age of the<br />
Lower Yezo Group and the upper part of the Sorachi Group in<br />
Hokkaido. In: Centenary of Japanese Micropaleontology.<br />
(Ishizaki, K. & Saito, T., Eds.). Terra Scientific Publishing<br />
Company, Tokyo, Japan. pp. 365-373.<br />
- 90 -<br />
The Lower Yezo Group and the Sorachi Group are distributed in<br />
the Sorachi-Yezo belt which trends N-S in Hokkaido, and the<br />
Kamuikotan Metamorphic Rocks also occur in this belt. The Lower<br />
Yezo Group consists of terrigenous rocks, and the Sorachi Group is<br />
composed mainly of green rocks and siliceous shale. The Lower Yezo<br />
Group overlies conformably the Sorachi Group. Radiolarian fossils<br />
occur in many localities of the Lower Yezo and Sorachi Groups. The<br />
age of these groups based on <strong>radiolaria</strong>n assemblages is as follows:<br />
The Lower Yezo Group is of late Hauterivian to early Albian age; the<br />
uppermost part of the Sorachi Group is equated with the late<br />
Hauterivian; and the lower upper part of the group is of Berriasian to<br />
early Hauterivian age.<br />
Tonielli, R. 1992. Two new <strong>radiolaria</strong>n species from the<br />
"Calcari Diasprigni" Fm of Mt. Terminilleto (RI).<br />
Paleopelagos, 2, 163-173.<br />
Middle to Late Jurassic radiolarite deposits are well-exposed in<br />
the Mt. Terminilletto succession. The study of <strong>radiolaria</strong>n<br />
assemblages led to the recognition of two new species. The<br />
stratigraphical distribution and taxonomic characters of the latter<br />
suggest that they possess a good biostratigraphic potential.<br />
Umeda, M., Goto, H. & Ishiga, H. 1992. MIddle<br />
Ordovician <strong>radiolaria</strong>ns from the Lachlan Fold Belt,<br />
southeastern Australia. Mem. Fac. Sci., Shimane Univ., 26,<br />
131-140.<br />
Umeda, M., Kugimiya, Y. & Ishiga, H. 1992. Late<br />
Triassic-Early Jurassic <strong>radiolaria</strong>ns from chert pebbles of the<br />
middle Miocene in northern part of Ooda City, Shimane<br />
Prefecture, Japan. Geol. Rep. Shimane Univ., 11, 71-76. (in<br />
Japanese)<br />
Vasicek, Z., Rehakova, D., Michalik, J.,<br />
Peterkáková, M. & Halásová, E. 1992. Ammonites,<br />
Aptychi, Nanno- and Microplankton from the lower<br />
Cretaceous Pieniny formation in the Kysuca Gate near Zilina<br />
(western Carpathian Klippen Belt, Kysuca Unit). Západné<br />
karpaty, Sér. Paleont., 16, 43-58.<br />
The outcrops in steep sides of the Rochovica and Brodnianska<br />
Hora hills squeezing the Kysuca Gate (a break of the Kysuca River<br />
into the Vah River Valley by Zilina) yield the classical sections of the<br />
Kysuca Unit of the Klippen Belt. The sequence of the "Rudina<br />
Klippe" overturned to the east crops out in the western end of the<br />
Varin section of the Klippen Belt between the Magura Unit on the<br />
north and the Manin Unit on the south. It consists of Aalenian to<br />
upper Turonian members. Jurassic/Cretaceous boundary beds<br />
cropping out in a quarry near the Brodno railway station dealt with<br />
more complete Lower Cretaceous sequence exposed along right side<br />
of the Kysuca River on the southern Rochovica foothill. This paper<br />
deals with the distribution of microfauna (Calpionellids, <strong>radiolaria</strong>ns<br />
and foraminifera), macrofauna (apticci and ammonites) and<br />
nannoplankton for the Jurassic-Cretaceous boundary.<br />
Vishnevskaya, V. 1992. Significance of Mesozoic<br />
<strong>radiolaria</strong>ns for tectonostratigraphy in Pacific Rim terranes of<br />
the former USSR. In: Significance and application of<br />
Radiolaria to terrane analysis. (Aitchison, J.C. & Murchey,<br />
B.L., Eds.), vol. 96/1-2. Special Issue: Palaeogeogr.<br />
Palaeoclimatol. Palaeoecol., Elsevier, Amsterdam. pp. 23-<br />
39.<br />
The application of new methods for the extraction of<br />
<strong>radiolaria</strong>ns from dense cherts, jaspers and tuffs in fold belts of the<br />
Far East USSR enables us to revise the lowest age limit of<br />
volcanogenic-siliceous rocks along the NW Pacific Rim from Late<br />
Jurassic to Early or Late Permian. The discovery of new <strong>radiolaria</strong>n<br />
localities in the Koryak Upland, Kamchatka allows determination of<br />
the age of siliceous rocks in several ophiolite belts and provides<br />
indications of paleolatitude in some terranes. Radiolarians have been<br />
extracted to aid in terrane analysis as well as geological-tectonic<br />
mapping and palinspastic reconstructions. High diversity Middle<br />
Cretaceous <strong>radiolaria</strong>n assemblages from some allochthons of North<br />
Kamchatka resemble those from Site 466 of Leg 62 and Site 585 of<br />
Leg 89 in the Pacific Ocean as well as some from low latitude Cuban<br />
sections. This may be considered as evidence for the large scale<br />
lateral tectonic dislocations of these blocks since the Aptian-early<br />
Albian.<br />
Wakita, K., Kojima, S., Okamura, Y., Natal'in,<br />
B. & Zyabrev, S.V. 1992. Triassic and Jurassic<br />
Radiolaria from the Khabarovsk complex, eastern Russia. In:<br />
Proceedings of the Third Radiolarian Symposium. (Sakai, T.
Radiolaria 14 Bibliography - 1992<br />
& Aita, Y., Eds.), vol. 8 . News of Osaka<br />
Micropaleontologists, special Volume, Osaka. pp. 9-19. (in<br />
Japanese)<br />
Middle Triassic and late Early to early Middle Jurassic<br />
<strong>radiolaria</strong>ns are extracted from the rocks in the Khabarovsk<br />
complex, at the outcrops to the south of the railway bridge over the<br />
Amur River near Khabarovsk, eastern Russia. The Khabarovsk<br />
complex is a tectonic melange which includes blocks and slices of<br />
chert, siliceous shale, sandstone, basalt, limestone, and psammitic<br />
and pelitic schists within sheared shale matrices.<br />
Two rock samples of reddish brown bedded chert yield Middle<br />
Triassic <strong>radiolaria</strong>ns, such as Triassocampe deweveri,<br />
Pseudostylosphaera cf. japonica and P. cf. tenue. One rock sample of<br />
reddish brown siliceous shale yields late Early Jurassic <strong>radiolaria</strong>ns,<br />
such as Hsuum hisuikyoense, Tricolocapsa plicarum and<br />
Eucyrtidiellum sp. A. Another rock sample of reddish brown siliceous<br />
shale yields early Middle Jurassic <strong>radiolaria</strong>ns, such as Tricolocapsa<br />
plicarum, T. (?) fusiformis and Stichocapsa japonica. These Jurassic<br />
<strong>radiolaria</strong>n assemblages are almost coeval with the Laxtorum (?)<br />
jurassicum Zone and Tricolocapsa plicarum Zone (MATSUOKA and<br />
YAO, 1986), respectively. Lithology, structure, and ages of the<br />
rocks in the Khabarovsk complex is very similar to those of the<br />
sedimentary complexes in the Mino terrane (central Japan) and in<br />
the Nadanhada region (Northeast China). The evidence suggests that<br />
the complexes of the three regions belong to a single disrupted<br />
terrane in Jurassic to early Cretaceous time.<br />
Wang, Y.J. & Yang, Q. 1992. Neogene and Quaternary<br />
<strong>radiolaria</strong>ns from Leg 125. In: Proceedings of the Ocean<br />
Drilling Program, Scientific Results. (Freyer, P., Pearce,<br />
J.A., Stokking, L.B. et al., Eds.), vol. 125. College<br />
Station, TX (Ocean Drilling Program), pp. 95-112.<br />
Radiolarians were recovered from three of the five holes<br />
investigated during Leg 125. Relative abundances are estimated at<br />
Holes 782A and 784A, where preservation is poor to good. Rare,<br />
poorly preserved <strong>radiolaria</strong>ns are present in Hole 786A. Seven<br />
<strong>radiolaria</strong>n zones are recognized in the latest early- middle Miocene<br />
to early Pleistocene of Holes 782A and 784A. These zones are<br />
approximately correlated to the zones of Sanfilippo and others<br />
published in 1985.<br />
Welling, L.A., Pisias, N.G. & Roelofs, A.K.<br />
1992. Radiolarian microfauna in the northern California<br />
Current System: indicators of multiple processes controlling<br />
productivity. In: Upwelling Systems: Evolution Since the<br />
Early Miocene. (Summerhayes, C.P., Prell, W.L. & Emeis,<br />
K.C., Eds.), vol. 64. Geological Society of London, special<br />
Publication, London, U. K. pp. 177-194.<br />
Radiolaria. as other plankton, appear to be highly tuned to<br />
specific oceanographic environments. Thus, in a transitional region<br />
such as the eastern North Pacific, where many different water<br />
masses are mixed, Radiolaria provide very sensitive tracers of these<br />
water masses and the currents that carry them. We present the first<br />
two years of <strong>radiolaria</strong>n results from the Multitracers sediment trap<br />
study across the northern California Current System. Three<br />
moorings. positioned along a transect at approximately 130, 280<br />
and 650 km from the coast. sample a wide variety of oceanographic<br />
conditions both spatially and temporally. Selected species or species<br />
groups are presented along with hydrographic data from the region in<br />
order to demonstrate the basic trends in the <strong>radiolaria</strong>n data and<br />
illustrate their relationships to fluctuations in their physical<br />
environment. Multiple linear regression is used to explore the<br />
relationship between <strong>radiolaria</strong>n composition and the export of<br />
carbon from this system.<br />
The most important physical process controlling variability in<br />
the <strong>radiolaria</strong>n composition along this transect is attributed to<br />
variability in the intensity of the southward-flowing California<br />
Current. The seasonality of the California Current is clearly<br />
reflected by changes in the composition of the <strong>radiolaria</strong>n trap<br />
assemblages; very different species dominate this region in summer<br />
as compared to winter. In addition to seasonal trends, evidence in<br />
both the offshore and onshore environments suggests significant<br />
differences between years. This region appears to have been more<br />
strongly influenced by cold. subarctic water during the winter of<br />
1988/1989 than during the previous year. The relationship between<br />
<strong>radiolaria</strong>n species abundances and the fluxe of organic carbon<br />
strongly indicates that a number of different oceanographic<br />
processes contribute to enhanced productivity at these sites. This<br />
has important implications when making inferences from the<br />
geological record about past changes in the intensity of upwelling in<br />
this eastern boundary current system.<br />
White, L.D., Garrison, R.E. & Barron, J.A. 1992.<br />
Miocene intensification of upwelling along the California<br />
- 91 -<br />
margin as recorded in siliceous facies of the Monterey<br />
Formation and offshore DSDP sites. In: Upwelling Systems:<br />
Evolution Since the Early Miocene. (Summerhayes, C.P.,<br />
Prell, W.L. & Emeis, K.C., Eds.), vol. 64. Geological<br />
Society of London, special Publication, London, U.K. pp.<br />
429-442.<br />
Diatomaceous sediments and their diagenetic equivalents in the<br />
Monterey Formation record a variable history of upwelling along the<br />
California margin. Distinctive dark opal-CT and quartz cherts found<br />
in distal basins of the Monterey Formation are the result of burial<br />
diagenesis of pure biosiliceous oozes (biosiliceous oozes without<br />
significant admixtures of clay) and arc therefore evidence of<br />
intensified coastal upwelling during the early middle Miocene. Dating<br />
of six sections of the Monterey Formation, Iargely by diatom<br />
biostratigraphy, suggests that at the Point Reyes and Point Año<br />
Nuevo sections in north-central California. the age of the earliest<br />
chert intervals is between 13.8 and 15.0 Ma. and 14.3 and 14.8<br />
Ma. respectively. In south-central California. ages from the Shell<br />
Beach, Mussel Rock. and Lions Head sections imply that the age of<br />
the base of the chert intervals is between 12.7 and 13.3 Ma. Both<br />
ages correlate to an early middle Miocene high latitude cooling step<br />
that resulted in more vigorous surface water circulation. upwelling of<br />
nutrient-rich waters, and increased biosiliceous sedimentation in the<br />
North Pacific. The north-south difference in age of the base of the<br />
chert interval probably reflects a progressive intensification of the<br />
California Current from 15.0 to 12.7 Ma.<br />
The age of the onset of biosiliceous sedimentation at DSDP<br />
sites of the northeastern Pacific is also generally younger at the<br />
more southern sites; however, these particular DSDP sites were<br />
located some distance from the centres of coastal upwelling and arc<br />
not as reliable indicators of the intensification of upwelling along the<br />
California margin.<br />
Widz, D. 1992. Datation par les radiolaires des radiolarites<br />
jurassiques de l'Unité de Grajcarek (Zone des Klippes de<br />
Pieniny, Carpathes occidentales, Pologne). Bull. pol. Acad.<br />
Sci. (Earth Sci.), 40/2, 115-124.<br />
The present study of the <strong>radiolaria</strong>n fauna collected from the<br />
Grajcarek Unit provides evidence for the presence of Upper Jurassic<br />
Unitary Associations: U.A. 7-8 (Kimmeridgian), U.A. 8 (Upper<br />
Oxfordian), U.A. 9 (Kimmeridgian). A correlation between eastern<br />
and western parts of the Grajcarek Unit has been established. The<br />
biostratigraphic age determination suggests the synchronous<br />
disappearance of radiolarites (Kimmeridgian) and distinctive<br />
diachronism of lithofacies within them<br />
Wu, H.R. & Pan, Z.P. 1992. Paleozoic sedimentary<br />
sequences and their tectonic setting discrimination in<br />
Western Junggar, Xingjiang, China. Adv. Geosci., 2, 246-<br />
274.<br />
In west Junggar. there are large areas of Paleozoic marine<br />
volcanic-sedimentary clastic sequence associated with ophiolite<br />
melange. Usually a normal sedimentary sequence is in fault-contact<br />
with an older ophiolitic complex. Petrographic sedimentary features<br />
indicate that they are deep-sea turbidites. Mineral and geochemical<br />
evidences. including QFL and QmFLT plots, SiO2 vs K2O/Na2O and<br />
SiO2 /AI2O 3 vs K2O/Na2O plots. TiO2 % ,AI2O 3 /SiO2 , K2O/Na2O, Al2O3 /(CaO/Na2O) vs +MgO% plots, and Th-Sc-Zr. Th-Co-<br />
Zr, La-Th-Sc, Ti/Zr-La/Sc plots. indicate the volcanic arc provenance<br />
for the clastic sequences and the sedimentary basins relating to<br />
oceanic island are . continental island are and active continental<br />
margin. It is clear that during the Paleozoic time there was a west<br />
Junggar ocean characterized by the complicated island arcs and<br />
deep water basins. This ocean might be a part of paleo-ocean<br />
between the Sibirian plate. Kazakhstan plate and Tarim plate. The<br />
variation from the Ordovician-Silurian oceanic island arc or<br />
undissected and transitional arc to the Devonian-Carboniferous<br />
continental island arc or dissected and transitional arc shows the<br />
moving of west Junggar ocean from pelagic environment toward<br />
continental margin.<br />
Yamamoto, K. 1992. Composition and diversity of<br />
<strong>radiolaria</strong>n fossil assemblages: Case study on Upper<br />
Cretaceous Futakawa Formation, Sotoizumi Group. In:<br />
Proceedings of the Third Radiolarian Symposium. (Sakai, T.<br />
& Aita, Y., Eds.), vol. 8 . News of Osaka<br />
Micropaleontologists, special Volume, Osaka. pp. 77-88. (in<br />
Japanese)<br />
Radiolarian fossil assemblages from the Upper Cretaceous<br />
Futakawa Formation, Sotoizumi Group, Southwest Japan were<br />
preliminary studied in order to clarify their composition, diversity<br />
and dominant species. Some methods of quantitative analysis for<br />
<strong>radiolaria</strong>n assemblages are used herein. Through this study, the<br />
assemblages from the Futakawa Formation were characterized by a
Bibliography - 1992 Radiolaria 14<br />
predominance of spumellarian individuals. This trend in composition<br />
was similar to those of the bathyal assemblages of Empson-Morin<br />
(1984). The Fisher α index (Fisher et al., 1943), the Morishita's, β<br />
index (Morishita, 1967), and the MacArthur model (Shimoyama,<br />
1989) were used to measure the diversity of <strong>radiolaria</strong>n<br />
assemblages. The β was better than the α in the quantitative<br />
analysis of <strong>radiolaria</strong>n assemblages. Each assemblage from the<br />
Futakawa Formation was commonly dominated by only a few species<br />
of spongy or sieve plate spumellarians which comprised about 80%<br />
of the total number of individuals.<br />
Yamaoka, Y. 1992. Meso - Paleozoic complex in northern<br />
part of Tsuyama City, Okayama Prefecture, Japan. Geol. Rep.<br />
Shimane Univ., 11, 77-86. (in Japanese)<br />
Yamashita, M., Ishida, K. & Ishiga, H. 1992.<br />
Palaeofusulina sinensis age for late Permian Neoalbaillella<br />
ornithoformis <strong>radiolaria</strong>n zone, southwest Japan. J. geol.<br />
Soc. Japan, 98/12, 1145-1148. (in Japanese)<br />
Yamato-Omine-Research-Group 1992. Paleozoic and<br />
Mesozoic systems in the central area of the Kii mountains,<br />
southwest Japan (Part 4). Mesozoic of the Takaharagawa<br />
district in Nara Prefecture. Earth Sci., J. Assoc. geol. Collab.<br />
Japan, 46/3, 185-198. (in Japanese)<br />
Yanagida, J., Ota, M. & Sano, H. 1992. Akiyoshi<br />
limestone group: Permo-Carboniferous organic reef complex.<br />
In: Paleozoic and Mesozoic Terranes: Basement of the<br />
Japanese Island Arcs. 29th IGC Field Trip Guide Book.<br />
(Adachi, M. & Suzuki, K., Eds.), vol. 1. Nagoya University,<br />
Nagoya, Japan. pp. 225-259.<br />
Yao, A., Adachi, M., Shibuya, H. & Setoguchi,<br />
T. 1992. Triassic and Jurassic sequences of the Mino Terrane<br />
in Central Japan. In: Paleozoic and Mesozoic Terranes:<br />
Basement of the Japanese Island Arcs. 29th IGC Field Trip<br />
Guide Book. (Adachi, M. & Suzuki, K., Eds.), vol. 1. Nagoya<br />
University, Nagoya, Japan. pp. 179-188.<br />
The Mino (Tamba-Mino-Ashio) terrane of central Japan is one of<br />
the major tectonostratigraphic terranes that constitute the pre-<br />
Tertiary basement of the Japanese Islands, and is thought to extend<br />
north to Sikhote-Alin and northeast China (Kojima, 1989). This<br />
Afanasieva, M.S. & Zamilatskaya, T.K. 1993. The<br />
paleobiogeography of the northeast Precaspian Basinand pre-<br />
Uralian Depression in artinskian time based on Radiolaria and<br />
Foraminifera. In: Radiolaria of giant and subgiant fields in<br />
Asia. Nazarov Memorial Volume. (Blueford, J.R. & Murchey,<br />
B.L., Eds.), Micropaleontology, special Publication vol. 6.<br />
Micropaleontology Press, American Museum of Natural<br />
History, New York. pp. 61-65.<br />
Three biogeographic zones of the Artinskian paleosea in the<br />
Pricaspian Basin and the pre-Uralian Depression were reconstructed<br />
by distinguishing <strong>radiolaria</strong>n paleobiocoenoses, analyzing the<br />
paleoecological distribution of foraminiferal associations, and<br />
comparing lithologic compositions. These zones are: 1, the northern<br />
margin of the Pricaspian Basin together with the western margin of<br />
the pre-Uralian Depression; 2, the eastern margin of the Pricaspian<br />
and pre-Uralian paleosea: and 3, the relatively deep-water basin. The<br />
paleoecologic conditions of the relatively shallow-water basin<br />
margins evidently were the most favorable for the existence of both<br />
<strong>radiolaria</strong>ns and benthonic foraminifera. The more impoverished<br />
<strong>radiolaria</strong>n and foraminifera associations in the relatively deepwater<br />
parts of the ancient sea suggest unfavorable environmental<br />
conditions.<br />
Aguado, R., Molina, J.M. & O'Dogherty, L. 1993.<br />
Bioestratigrafía y litoestratigrafía de la formación carbonero<br />
(Barremiense-Albiense?) en la transición Externo-Subbético<br />
Medio. Cuad. Geol. ibérica, 17, 325-344.<br />
The biostratigraphy and lithostratigraphy of the Carbonero Fm.<br />
(Upper Barremian-Lower Albian?), in the transition between the<br />
External Subbetic and the Middle Subbetic (S of the Jaen province)<br />
have been analysed. In this formation three members have been<br />
recognized according to their lithologic characterisation. The age of<br />
each one of its three members has been stated precisely with<br />
calcareous nannoplankton, Radiolaria and planktonic Foraminifera.<br />
1993<br />
- 92 -<br />
terrane is represented by Late Paleozoic-Mesozoic complex which<br />
consists essentially of Carboniferous-Permian greenstone<br />
limestone-chert, Triassic-Jurassic chert, Early-Middle Jurassic<br />
siliceous mudstone, and Middle Jurassic to earliest Cretaceous<br />
clastic rocks. This sedimentary complex was produced by an<br />
accretionary process during Jurassic to earliest Cretaceous time<br />
(e.g. Mizutani, 1990). This field trip concentrates on observation of<br />
continuous Triassic-Jurassic chert-clastic sequences on the river<br />
bed and bank along the Kiso River in the Inuyama area and the Hida<br />
River in the Kamiaso area, Gifu Prefecture (Fig. 1). The trip includes<br />
a visit to the Kamiaso conglomerate (Adachi, 1971), in which the<br />
oldest geologic record (2050 Ma) in the Japanese Islands was<br />
detected by Rb-Sr whole-rock age determination (Shibata and Adachi,<br />
1974). Discussions will emphasize lithostratigraphy, <strong>radiolaria</strong>n<br />
biostratigraphy, paleomagnetism and sedimentary environments of<br />
the chert-clastic sequences.<br />
Yeh, K.Y. 1992. Triassic Radiolaria from Uson Island,<br />
Philippines. Bull. natl. Mus. nat. Sci., Taiwan, 3, 51-91.<br />
Triasic <strong>radiolaria</strong>n faunas were discovered from the bedded<br />
cherts of Uson Island, North Palawan Block, Philippines. By<br />
correlating with the <strong>radiolaria</strong>ns from previous studies, the ages of<br />
Uson <strong>radiolaria</strong>n faunas are dated as late Ladinian, late Carnian, late<br />
Norian, and early Rhaetian, respectively. This report illustrates the<br />
major <strong>radiolaria</strong>n taxa from Uson Island discovered in this study.<br />
Only those forms with better preservation were described herein.<br />
The bedded cherts in Uson Island are lithologically similar to those in<br />
the Busuanga Island. It is believed that the Uson cherts are parts of<br />
the Liminangcong chert which is widely distributed in the North<br />
Palawan Block. Only Triassic <strong>radiolaria</strong>ns have been discovered from<br />
Uson Island. The results of this study indicate that the upper Upper<br />
Triassic (Rhaetian) section of the Liminangcong chert exists in Uson<br />
Island.<br />
Zhang, K., Wu, S. & Liu, Y. 1992. Radiolarians and<br />
Conodonts from the Dalong Formation at Hushan of Nanjing<br />
and their Facieological significance. Earth Sci., J. China<br />
Univ. Geosci., 17/3, 295-300. (in Chinese)<br />
The <strong>radiolaria</strong>n and conodont fauna dealt with in the paper were<br />
collected from Hushan near Nanjing City. This fauna comprises 8<br />
species belonging to 6 genera of <strong>radiolaria</strong>ns and 12 species<br />
belonging to 7 genera of conodonts. One <strong>radiolaria</strong>n species is new<br />
namely Stauroplegma nanjingensis (sp. nov.). The characteristics of<br />
the fauna and its environmental significance have been discussed.<br />
The Dalong Forrnation is proved to be of deep-water shelf facies.<br />
Three nannoplankton zones have been recognized: Micrantholithus<br />
hoschulzii (Upper Barremian), Hayesites irregularis (Lower Aptian)<br />
and Rhagodiscus angustus (Upper Aptian-Lower Albian). The<br />
determined <strong>radiolaria</strong>n association is characteristically of Lower<br />
Aptian age. According to these bio stratigraphic and lithologic data<br />
the Carbonero Fm is correlated with the Lower Member (Member I) of<br />
the Fardes Fm.<br />
Aitchison, J.C. 1993a. Albaillellaria from the New<br />
England orogen, Eastern NSW, Australia. In: Interrad VI.<br />
(Lazarus, D.B. & De Wever, P., Eds.), vol. 21/4. Special<br />
Issue: Marine Micropal., Elsevier, Amsterdam. pp. 353-367.<br />
Radiolarian data provide important age constraints on the<br />
development of terranes within the New England orogen and have<br />
implications for existing tectonic models. Most <strong>radiolaria</strong>n<br />
assemblages recovered from the orogen are of Late Devonian to<br />
Early Carboniferous ages. Albaillellaria comprise a minor proportion<br />
of the faunas present but have major biostratigraphic significance.<br />
Holoeciscus Foreman, Helenifore Nazarov and Ormiston,<br />
Circulaforma Cheng, Ceratoikiscum Deflandre, Protoalbaillella<br />
Cheng, and Albaillella Deflandre, two new genera and three new<br />
species are found at various stratigraphic levels. Eleven <strong>radiolaria</strong>n<br />
assemblages are recognised. In stratigraphic order these are the<br />
Helenifore laticlavium-Ceratoikiscum planistellare, Protoholoeciscus<br />
hindea, Holoeciscus formanae, Paraholoeciscus bingaraensis,<br />
Ceratoikiscum umbraculum, Protoalbaillella anaiwanensis, Albaillella<br />
paradoxa, Albaillella undulata-Albaillella indensis, Albaillella<br />
indensis-Albaillella furcata, Albaillella cartalla-Albaillella thomasi<br />
and Circulaforma omicron assemblages. There is an apparent<br />
biostratigraphic succession amongst the Albaillellaria in the New<br />
England orogen in which Protoholoeciscus hindea n. gen. n. sp. is<br />
transitional between Ceratoikiscum Deflandre and Holoeciscus<br />
Foreman and Paraholoeciscus bingaraensis n. gen. n. sp. is<br />
transitional between Holoeciscus Foreman and the Albaillella<br />
paradoxa Deflandre group.
Radiolaria 14 Bibliography - 1993<br />
Aitchison, J.C. 1993b. Devonian (Frasnian) Radiolarians<br />
from the Gogo Formation, Canning Basin, Western Australia.<br />
Palaeontographica Abt. A, 228, 105-128.<br />
A diverse and remarkably well-preserved Frasnian <strong>radiolaria</strong>n<br />
fauna is described from carbonate concretions of the Gogo<br />
Formation, Canning Basin, Western Australia. It is the best<br />
preserved, most diverse Frasnian assemblage yet documented with<br />
57 species (41 new) assigned to 14 genera described. All elements<br />
of the fauna are common but it is dominated by ceratoikiscids of<br />
which 11 are new species. New species described include:<br />
Ceratoikiscum patagiatum n.sp., Ceratoikiscum spiculatum n.sp.,<br />
Ceratoikiscum fragile n.sp., Ceratoikiscum canningense n. sp.,<br />
Ceratoikiscum robustum n. sp., Ceratoikiscum marginatum n. sp.,<br />
Ceratoikiscum echinatum n. sp., Ceratoikiscum torale n.sp.,<br />
Ceratoikiscum stellatum n.sp., Ceratoikiscum pillaraense n.sp.,<br />
Helenifore gogoense n.sp., Entactinia hystricousa n.sp., Entactinia<br />
gogoense n. sp., Entactinia aperticuvas n. sp., Entactinia pillaraense<br />
n. sp., Entactinia profundisulcus n. sp., Entactinia proceraspina n.sp.,<br />
Entactinosphaera australis n.sp., Entactinosphaera aculeatissime<br />
n.sp., Entactinosphaera? robusta n.sp., Spongentactinia concinna n.<br />
sp., Spongentactinia exquisita n. sp., Polyentactinia invenusta n. sp.,<br />
Polyentactinia tenera n. sp., ? Astroentactinia radiata n. sp.,<br />
Helioentactinia stellaepolus n.sp., Helioentactinia aster n.sp.,<br />
Somphoentactinia cavata n.sp., Spongentactinella intracta n.sp.,<br />
Spongentactinella abstrusa n.sp., Seccuicollacta labyrinthica n.sp.,<br />
Secuicollacta araneam n.sp., Palaeoscenidium venustum n.sp.,<br />
Palaeoscenidium robustum n.sp., Palaeoscenidium echinatum n.sp.,<br />
Palaeoscenidium nudum n.sp., Palaeoscenidium daktylethra n.sp.,<br />
Palaeoscenidium tabernaculum n.sp., Palaeoscenidium phalangium n.<br />
sp., Palaeoscenidium delicatum n.sp., Paleotripus gogense n. sp.<br />
Alder, V.A. & Boltovskoy, D. 1993. The ecology of<br />
larger microzooplankton in the Weddell-Scotia confluence<br />
area: horizontal and vertical distribution patterns. J. marine<br />
Res., 51/2, 323-344.<br />
The distribution of microzooplankton >15µm (large<br />
dinoflagellates, foraminifers, <strong>radiolaria</strong>ns, tintinnids,<br />
microcrustaceans and various Invertebrate larvae) was studied in<br />
samples retrieved from 10 to 400 m in two overlapping transects<br />
along 49 W, between 57°S and 61°30'S (27 Nov.-12 Dec. 1988, and<br />
27 Dec. 1988-4 Jan. 1989). For each sample approx. 10 litres of<br />
water were concentrated with a 15 µm-mesh sieve and counted<br />
under an inverted microscope. Biomass estimates were based on<br />
measurements of cell dimensions. Dinoflagellates and tintinnids<br />
concentrated at 50-90 m (10-400 m weighted averages,<br />
dinoflagellates: 103 ind./l, 131 mg C/m 2 ; tintinnids: 9.7 ind./l, 53<br />
mg C/m 2 ). Copepod nauplii had a more variable vertical pattern with<br />
maximum numbers at 100-200 m (10-400 m av.: 2.6 ind./l, 27 mg<br />
C/m 2 ). Foraminifers and <strong>radiolaria</strong>ns were most abundant in<br />
noticeably deeper waters peaking below 150 m (10-400 m av.,<br />
foraminifers: 0.2 ind./l, 11 mg C/m2; <strong>radiolaria</strong>ns: 2.7 ind./l, 12 mg<br />
C/m 2 ). Large dinoflagellates accounted, on the average, for 55% of<br />
the biomass of the heterotrophs considered in the 10-400 m layer,<br />
followed by the tintinnids (23%), Copepod nauplii (11%),<br />
foraminifers (5X), and <strong>radiolaria</strong>ns (5X). The 100-400 m layer<br />
hosted up to 87% (mean: 49X) of total 10-400 m integrated<br />
microzooplanktonic biomass, and limited data for depths over 400 m<br />
indicate that these strata can contribute significantly (up to 50%)<br />
to total organic carbon, especially at the less fertile locales. The<br />
distribution of loricate ciliates was strongly correlated with those of<br />
chlorophyll a, and especially dinoflagellates (r=0.832, for logtransformed<br />
data), suggesting close trophic relationships between<br />
these two groups. The northern sites were generally richer in<br />
microzooplankton than the area closer to the ice-edge, and the<br />
southernmost ice-covered zone yielded the lowest microplanktonic<br />
values. This biological pattern, which was but loosely coupled with<br />
the Weddell-Scotia Confluence, with the vertical stability of the<br />
water column, and with near surface concentrations of chlorophyll a,<br />
can at least partly be explained by differential grazing pressure by<br />
crustacean mesozooplankton. The time elapsed between the two<br />
transects did not affect the microzooplanktonic assemblages<br />
noticeably. Comparisons with previous abundance estimated carried<br />
out earlier and later in the growth season suggest that<br />
microzooplanktonic abundances increase toward the late summerfall,<br />
probably In response to enhanced availability of nano- and picosized<br />
producers, characteristic of Antarctic post-bloom conditions.<br />
Amon, E.O. 1993. Cretaceous Radiolaria of the Urals. In:<br />
Radiolaria of giant and subgiant fields in Asia. Nazarov<br />
Memorial Volume. (Blueford, J.R. & Murchey, B.L., Eds.),<br />
Micropaleontology, special Publication vol. 6 .<br />
Micropaleontology Press, American Museum of Natural<br />
History, New York. pp. 66-71.<br />
Radiolarians have a wide distribution in Cretaceous deposits<br />
from the Great Urals region of the Russia eastern slope of the Urals,<br />
and adjacent areas of the West Siberian plate. In the local area there<br />
are 10 preliminary <strong>radiolaria</strong>n zones that can be distinguished.<br />
- 93 -<br />
Understanding the geologic history of this area requires a more<br />
intense geographic and stratigraphic distribution study of<br />
<strong>radiolaria</strong>ns, including correlation with the Russian Platform and<br />
Atlantic Basin with respect to species and assemblage.<br />
Anderson, O.R. 1993. The trophic role of planktonic<br />
foraminifera and <strong>radiolaria</strong>. Marine Microbial food Webs,<br />
7/1, 31-51.<br />
Planktonic foraminifera and <strong>radiolaria</strong> are abundant in diverse<br />
oceanic locations and at varying depths in the water column. They<br />
are largely opportunistic feeders and generalists taking a wide<br />
variety of prey spanning monera (eubacteria and cyanobacteria) to<br />
protista and metazoan zooplankton (copepods, Larvacea, etc.).<br />
Juvenile and adults of small species generally consume algal or<br />
protistan prey. Most of the larger species of planktonic foraminifera,<br />
and some <strong>radiolaria</strong>, are omnivorous based on current evidence. One<br />
planktonic foraminiferan (Hastigerina pelagica) is carnivorous,<br />
consuming zooplankton prey. Data on predators is limited, but based<br />
on digestive tract samples from diverse geographic locations,<br />
planktonic foraminifera and <strong>radiolaria</strong> have been detected in<br />
tunicates (e.g., salps), crustacea such as copepods and euphausids,<br />
and in certain penaeidae, among others. The co-occurrence of<br />
diverse species of planktonic foraminifera and <strong>radiolaria</strong> in the same<br />
locale suggests that these species do not differ substantially in<br />
their trophic competitiveness. Furthermore, the presence of algal<br />
symbionts (providing a primary source of nutrition), approximately<br />
similar longevity, and lie-in-wait predatory strategies make them<br />
trophically complementary rather than differentially competitive,<br />
thus possibly accounting for their local diversity and high<br />
abundance.<br />
Bak, M. 1993a. Micropaleontological and Statistical<br />
Analyses of the Albian and Cenomanian deposits based on<br />
Radiolaria, Pieniny Klippen Belt, Carpathians. Bull. pol.<br />
Acad. Sci. (Earth Sci.), 41/1, 13-22.<br />
Fifty three species of Radiolaria from the Upper Albian-Lower<br />
Cenomanian marly deposits of the Czorsztyn and Branisko<br />
successions have been statistically analysed. Interdependence<br />
between diversification of <strong>radiolaria</strong>n faunas and black shale (anoxic<br />
events) deposition was found. These Radiolaria assemblages<br />
represent the Acaeniotyle umbilicata Zone.<br />
Bak, M. 1993b. Late Albian-early Cenomanian Radiolaria<br />
from the Czorsztyn succession Pieniny Klippen Belt,<br />
Carpathians. In: Geology of the Pieniny Klippen Belt,<br />
Carpathians, Poland. (Birkenmajer, K., Eds.), vol. 102.<br />
Studia geologica polonica, Crakow, Poland. pp. 177-207.<br />
Fifty three species of Radiolaria from the Upper Albian-Lower<br />
Cenomanian marly deposits of the Czorsztyn Succession have been<br />
analysed. The species determined belong to the orders Spumellaria<br />
(12 species) and Nassellaria (41 species). The investigated<br />
Radiolaria assemblages represent the Acaeniotyle umbilicata Zone.<br />
Baumgartner, P.O. 1993. Early Creataceous <strong>radiolaria</strong>ns<br />
of the Northeast Indian Ocean (Leg 123: Sites 765, 766 and<br />
DSDP Sites 261): The Antarctic-Tethys connection. In:<br />
Interrad VI. (Lazarus, D.B. & De Wever, P., Eds.), vol. 21.<br />
Special Issue: Marine Micropal., Elsevier, pp. 329-352.<br />
During ODP Leg 123, abundant and well-preserved Neocomian<br />
<strong>radiolaria</strong>ns were recovered at Site 765 (Argo Abyssal Plain) and<br />
Site 766 (lower Exmouth Plateau). Assemblages are characterized<br />
by the numerical dominance of a small number of non-tethyan forms<br />
and by the scarcity of tethyan taxa. Remarkable contrasts exist<br />
between <strong>radiolaria</strong>n assemblages extracted from claystones of Site<br />
765 and reexamined DSDP Site 261, and faunas recovered from<br />
<strong>radiolaria</strong>n sand layers, only found at Site 765. Clay faunas are<br />
unusual in their low diversity of apparently ecologically tolerant ( or<br />
solution resistant?), ubiquist species, whereas sand faunas are<br />
dominated by non-tethyan taxa. Comparisons with Sites 766 and<br />
261, as well as sedimentological observations, lead to the<br />
conclusion that this faunal contrast resulted from a difference in<br />
provenance, rather than from hydraulic sorting or selective<br />
dissolution.<br />
The ranges of 27 tethyan taxa from Site 765 were compared to<br />
the tethyan <strong>radiolaria</strong>n zonation by Jud (1991) by means of the<br />
Unitary Associations Method. This calculation allows to directly date<br />
the Site 765 assemblages and to estimate the amount of truncation<br />
of ranges for tethyan taxa. Over 70% of the already few tethyan<br />
species of Site 765, have truncated ranges during the Valanginian-<br />
Hauterivian. Radiolarian assemblages recovered from claystones at<br />
Sites 765 and 261 in the Argo Basin apparently reflect restricted<br />
oceanic conditions during the latest Jurassic-Barremian. Neither<br />
sedimentary facies nor faunal associations bear any resemblance to
Bibliography - 1993 Radiolaria 14<br />
what we know from typical tethyan sequences. We conclude that the<br />
Argo Basin was paleoceanographically separated from the Tethys<br />
during the Late Jurassic and part of the Early Cretaceous by its<br />
position at higher paleolatitudes and/or by enclosing land masses.<br />
Assemblages recovered from <strong>radiolaria</strong>n sand layers are<br />
dominated by non-tethyan species that are interpreted as<br />
circumantarctic. Their first appearance in the late Berriasian-early<br />
Valanginian predates the oceanization of the Indo-Australian<br />
breakup (Ml l, late Valanginian), but coincides with a sharp increase<br />
in margin-derived pelagic turbidites. The Indo-Australian rift zone<br />
and the adjacent margins must have been submerged deeply enough<br />
to allow an intermittent influx of circumantarctic cold water into the<br />
Argo Basin, creating increased bottom current activity. Cold-water<br />
<strong>radiolaria</strong>ns carried into the Argo Basin upwelled along the margin,<br />
died, and accumulated in radiolarite layers due to winnowing by<br />
bottom currents. High rates of faunal change and the sharp increase<br />
of bottom current activity are thought to be synchronous with<br />
possible pronounced late Berriasian-early Valanginian lowstands in<br />
sea level. Hypothetically, both phenomena might have been caused<br />
by a tendency to glaciation on the Antarctic-Australian continent,<br />
which was for the first time isolated from the rest of Gondwana by<br />
oceanic seaways as a result of Jurassic-Early Cretaceous sea-floor<br />
spreading.<br />
The absence of most typical tethyan <strong>radiolaria</strong>n species during<br />
the Valanginian-Hauterivian is interpreted as reflecting a time of<br />
strong influx of circumantarctic cold water following oceanization (M<br />
11) and rapid spreading between Southeast India and West<br />
Australia.<br />
The reappearance and gradual abundance/diversity increase of<br />
tethyan taxa, along with the still dominant circumantarctic species<br />
are thought to result from overall more equitable climatic conditions<br />
during the Barremian-early Aptian and from the establishment of an<br />
oceanic connection with the Tethys Ocean during the early Aptian.<br />
Blome, C.D. & Reed, K.M. 1993. Acid processing of<br />
pre-Tertiary <strong>radiolaria</strong>n cherts and its impact on faunal<br />
content and biozonal correlation. Geology, 21/2, 177-180.<br />
The numbers of <strong>radiolaria</strong>ns visible in thin sections of chertrich<br />
rocks are commonly an order of magnitude greater than the<br />
numbers observed on the surfaces of fragments etched by<br />
hydrofluoric acid (HF) and typically orders of magnitude greater than<br />
the numbers of individuals found in HF-processed residues.<br />
Destruction of <strong>radiolaria</strong>ns during both diagenesis and HF processing<br />
severely reduces faunal abundance and diversity and affects the<br />
taxonomic and biostratigraphic utility of chert residues. The robust<br />
forms that survive the processing represent only a small fraction of<br />
the death assemblage, and delicate skeletal structures used for<br />
species differentiation, commonly preserved in limestone <strong>radiolaria</strong>n<br />
faunas, are either poorly preserved or dissolved in many coeval<br />
chert residues. First and last occurrences of taxa in chert<br />
sequences are likely to be coarse approximations of their true<br />
stratigraphic ranges. Precise correlation is difficult between<br />
biozonations based solely on index species from cherts and those<br />
constructed from limestone faunas. Careful selection of samples in<br />
sequence, use of weaker HF solutions, and study of both chert and<br />
limestone faunas should yield better biostratigraphic information.<br />
Blueford, J. & Murchey, B. 1993. Radiolaria of giant<br />
and subgiant fields in Asia. Nazarov Memorial Volume.<br />
Micropaleontology Press Special Publication, vol. 6.<br />
American Museum of Natural History , 200 p.<br />
Throughout geologic time <strong>radiolaria</strong>ns have been major<br />
contributors to world-wide siliceous deposits. Their robust skeletons<br />
make them excellent candidates for preservation. The fact that<br />
<strong>radiolaria</strong>ns can be traced in abundance back to the Ordovician with<br />
unique evolutionary sequences, coupled with their planktonic<br />
lifestyles that are indicative of various paleoenvironmental<br />
conditions, make them ideal microfossils for stratigraphy and basin<br />
analysis. In this volume, workers from Russia, China, and Japan<br />
outline the usefulness of rads in stratigraphy, petrography, and<br />
paleoenvironmental interpretations.<br />
This book highlights the <strong>radiolaria</strong>ns found in important<br />
hydrocarbon basins in the East Eurasian continent. Many of the<br />
papers reflect an English summary of years of work by the authors<br />
of this book. Originally this book was proposed as a collection of<br />
papers in honor of Dr. Boris Nazarov, a pioneer in using Paleozoic<br />
<strong>radiolaria</strong>ns. However, the recent opening of the former Soviet Union<br />
to the outside put an urgency on obtaining information about these<br />
basins. We then decided to weave a story about how <strong>radiolaria</strong>ns are<br />
not only important in determining stratigraphy but also in evaluating<br />
the paleoenvironments of these important hydrocarbon yielding<br />
basins.<br />
Blueford, J.R. & Amon, E.O. 1993. Comparing<br />
elongated Spongodiscoidea (Radiolaria) from early Eocene<br />
- 94 -<br />
deposits of Turgay, Russia, with present world-wide<br />
distribution. In: Radiolaria of giant and subgiant fields in<br />
Asia. Nazarov Memorial Volume. (Blueford, J.R. & Murchey,<br />
B.L., Eds.), Micropaleontology, special Publication vol. 6.<br />
Micropaleontology Press, American Museum of Natural<br />
History, New York. pp. 72-89.<br />
Radiolarians can be reliable paleoceanographic indicators.<br />
"Spongy" <strong>radiolaria</strong>ns can be used to determine the environment of<br />
deposition of the early Eocene Tassaranskaya Formation in the<br />
northern Turgay area of Russia when compared to their present day<br />
distribution. The Turgay fauna shows similarities with faunas from<br />
other northern deposits during the Late Cretaceous through<br />
Paleogene. Of particular interest are the abundant elongated<br />
spongodiscoids found in the Tassaranskaya Formation. If recent<br />
studies on spongodiscoid distribution are accurate analogous to<br />
paleoenvironmental interpretation, the presence of these forms<br />
indicate a shallow, wind driven upwelling system with periods of<br />
warm water invasions. Elongated spongy <strong>radiolaria</strong>ns are helpful in<br />
reconstructing the depositional history of paleobasins. This paper<br />
taxonomically defines the early Eocene elongated spongodiscoids in<br />
the Turgay region so researchers can more easily compare data from<br />
this area. This study is an example of how paleoceanographic and<br />
paleoenvironmental information can be derived when spongy<br />
<strong>radiolaria</strong>ns are found.<br />
Blueford, J.R. & Gonzales, J. 1993. Selected<br />
sedimentary basins on the eastern Eurasian continent. In:<br />
Radiolaria of giant and subgiant fields in Asia. Nazarov<br />
Memorial Volume. (Blueford, J.R. & Murchey, B.L., Eds.),<br />
Micropaleontology, special Publication vol. 6 .<br />
Micropaleontology Press, American Museum of Natural<br />
History, New York. pp. 3-8.<br />
The eastern Eurasian continent has experienced several<br />
tectonic events throughout geologic time. The sedimentary basins<br />
that were formed as a consequence of plate interactions range in<br />
size, form, content and sedimentary evolution. The ages range from<br />
the Proterozoic to the Neogene and represent sedimentary basin fill<br />
from clastics, reefal, deep sea carbonates and silicates, to shallow<br />
water silicates. This area is a vast territory that includes Russia,<br />
China, Japan, India and other Far East countries. This area has been<br />
neglected in the English literature, but it is key to reconstructing<br />
global paleoceanographic patterns. The purpose of this paper is to<br />
summarize those basins that are mentioned in the volume and to<br />
provide geologic background. Since <strong>radiolaria</strong>ns are present in many<br />
of the evolving basins of the Phanerozoic, they are of great<br />
importance to understanding the depositional histories of many<br />
Eurasian basins.<br />
Boltovskoy, D., Alder, V.A. & Abelmann, A.<br />
1993. Annual flux of Radiolaria and other shelled plankters in<br />
the eastern equatorial Atlantic at 853 m: seasonal variations<br />
and Polycystine species-specific response. Deep-Sea Res.<br />
Part A, oceanogr. Res. Pap., 40/9, 1863-1895.<br />
Polycystine <strong>radiolaria</strong>ns, phaeodarians, tintinnids, tintinnid<br />
cysts and molluscs (chiefly pteropod protoconchae) were counted in<br />
20 time-series sediment trap samples retrieved in the eastern<br />
equatorial Atlantic (01 47.5'N, 11 07.6'W) at 853 m, between 1<br />
March 1989 and 16 March 1990. In addition, polycystine species<br />
were identified. Mean annual flux rates, in ind./m 2 /day, were:<br />
polycystines: 28,446, tintinnids: 27,275, foraminifers: 17,816,<br />
tintinnid cysts: 14,632, phaeodarians: 1370, and molluscs: 1192.<br />
These yields are noticeably higher than most previous data from<br />
various areas of the World Ocean, which in part is attributed to the<br />
coverage of particles
Radiolaria 14 Bibliography - 1993<br />
however, were also relatively small and would not be expected to<br />
bias the sedimentary record toward restricted periods of higher<br />
<strong>radiolaria</strong>n output. Comparison of the present data with detailed<br />
previous information for the Gulf of Alaska shows that both total<br />
<strong>radiolaria</strong>n flux, and its intermittence throughout the year, are very<br />
similar in the two areas.<br />
Boltovskoy, D., Alder, V.A. & Abelmann, A.<br />
1993. Radiolarian sedimentary imprint in Atlantic equatorial<br />
sediments: Comparison with the yearly flux at 853m. Mar.<br />
Micropaleontol., 23/1, 1-12.<br />
Radiolarian specific compositions in a series of 20 sediment<br />
trap samples covering an entire year (1.3.1989 to 16.3.1990,<br />
collected at 853 m) were compared with bottom (0-1 cm) materials<br />
from the same site (eastern equatorial Atlantic: 01°47.5'N,<br />
11°07.6'W). Data on mean sediment accumulation rates at the site<br />
of the mooring (I.59 -g/cm 2 /kyr), mean <strong>radiolaria</strong>n flux at 853 m<br />
(28,446 shells/m 2 /day), and abundance in the 0-1 cm bottom layer<br />
(48,258 shells/g) suggest that approximately 95% of the<br />
<strong>radiolaria</strong>ns produced are lost to the fossil record. Sediment trap<br />
sample-to-sample correlations (based on relative abundances of 40<br />
<strong>radiolaria</strong>n species present at levels ≥1% in at least one sample,<br />
mean value, r=0.886) did not differ significantly from correlations<br />
between each water column sample and surface sediments (mean<br />
r=0.878). Similarities between the flux and the sediments were not<br />
associated with time of year and with periods of enhanced<br />
<strong>radiolaria</strong>n output. Two taxa had lower, and nine taxa had higher<br />
percentage contributions in the sediments than in any one sediment<br />
trap sample, and a few of the abundant species had averages up to 7<br />
times higher in either the water column or the sediments. These<br />
dissimilar percentage loadings are attributed to selective<br />
dissolution, lateral subsurface and deep advection of shells from<br />
higher-latitude areas, and identification biases. As opposed to<br />
species-level inventories, family-level databases (including shells<br />
identified to family only ) differed significantly between the water<br />
column and the sediments. Spumellaria (especially Spongodiscidae)<br />
were more abundant in the sediments (35%) than in the water<br />
column (19%), while Nassellaria showed the opposite trend (64%<br />
and 80%, respectively). It is suggested that ease of identification of<br />
spongodiscid fragments and fragility of juvenile nassellarians are<br />
responsible for these differences.<br />
Braun, A. 1993. Die Anwendung der Radiolarien-<br />
Biochronologie auf Gesteine des Thüringischen Unterkarbons<br />
- Ergebnisse und Möglichkeiten. Geol. Jb. Hessen, 121, 11-<br />
16.<br />
Radiolarian faunas from Phosphorite-concretions of the<br />
"Ruβschiefer" and from Siderite concretions ("Kieskälber") of the<br />
roof slates in the Thuringian Lower Carboniferous allow dating and<br />
correlation of the Thuringian sediment series with those of the<br />
eastern Rheinisches Schiefergebirge. The level of the "Ruβschierer"<br />
contains the same Radiolarian zones as the "Liegende<br />
Alaunschiefer" of the Rheinisches Schiefergebirge. The deeper part<br />
of the "Dachschierer-Folge" corresponds biostratigraphically to the<br />
deeper part of the "Schwarze Lydite" of the Rheinisches<br />
Schiefergebirge.<br />
Braun, A. & Amon, E.O. 1993. A rapid technology of<br />
detecting and preliminary investigating of <strong>radiolaria</strong>ns in<br />
field work conditions. Paleont. Z., Akad. Nauk SSSR, 2, 122.<br />
(in Russian)<br />
A method for etching the surfaces of various sedimentary<br />
rocks, including <strong>radiolaria</strong>n. cherts, in field-work conditions is<br />
proposed. Solution of hydrofluoric acid can be used for this<br />
procedure.<br />
Braun, A. & Schmidt-Effing, R. 1993. Biozonation,<br />
diagenesis and evolution of <strong>radiolaria</strong>ns in the Lower<br />
Carboniferous of Germany. In: Interrad VI. (Lazarus, D.B. &<br />
De Wever, P., Eds.), vol. 21/4. Special Issue: Marine<br />
Micropal., Elsevier, Amsterdam. pp. 369-383.<br />
Based on <strong>radiolaria</strong>n faunas recovered from sequences of<br />
siliceous shales and dark claystones in the Lower Carboniferous of<br />
the Rheinisches Schiefergebirge (Germany), a <strong>radiolaria</strong>n biozonation<br />
is proposed. Diagenetic alteration of faunas is documented and the<br />
stratigraphic distribution of more resistant taxa is given. For closely<br />
spaced samples a gradual shift of morphotype abundance has been<br />
found for Albaillella cartalla in the Visean, but no gradual transition<br />
between species of Albaillella has been found.<br />
Carter, E.S. 1993. Biochronology and paleontology of<br />
uppermost triassic (Rhaetian) <strong>radiolaria</strong>ns, Queen Charlotte<br />
- 95 -<br />
Islands, British Columbia, Canada. Mem. Geol. (Lausanne),<br />
vol. 11, 1-175.<br />
A rich <strong>radiolaria</strong>n fauna of Rhaetian age has been recovered<br />
from limestone concretions in strata of the Sandilands Formation at<br />
localities on northwest Graham Island (Kennecott Point), Louise<br />
Island, Skidegate Inlet, and Kunga Island, Queen Charlotte Islands,<br />
British Columbia. Unusually thick stratigraphic sections at<br />
Kennecott Point and Kunga Island record continuous sedimentation<br />
through latest Triassic and earliest Jurassic time. Independent<br />
dating is provided by conodonts that co-occur in many <strong>radiolaria</strong>n<br />
samples and rare ammonoids that are associated at several levels.<br />
New <strong>radiolaria</strong>n zonation for the Rhaetian defined by Unitary<br />
Associations (UA.; Guex 1977, 1991) is presented. A database<br />
recording the appearance of 136 species in 69 superposed horizons<br />
or samples of 6 sections was used to establish 27 successive U A.,<br />
with each U A. defined by the totality of its characteristic species.<br />
UA's. were grouped into 6 distinct assemblages (biochronozones)<br />
whose terminology follows Carter 1990.<br />
The late Norian Betracciun deweveri Zone (Blome 1984) ranges<br />
into post-Monotis basal strata of the Sandilands Formation (late<br />
Norian or earliest Rhaetian). Immediately above this zone, three<br />
successive <strong>radiolaria</strong>n assemblages occur whose age is correlated<br />
with Late Triassic ammonoid biochronology of Tozer (1979).<br />
Assemblage 1, the lower one, approximates the lower part of the<br />
Amoenum Zone; Assemblage 2 (with four subassemblages)<br />
approximates the middle and upper Amoenum Zone; and Assemblage<br />
3 is correlated with the uppermost Triassic Crickmayi Zone.<br />
Two formal zones are established which allow worldwide<br />
correlation of the Rhaetian using <strong>radiolaria</strong>ns. Their ages are<br />
correlative with the Late Triassic ammonoid biochronology of Tozer<br />
(1979). The Proparvicingula moniliformis Zone contains <strong>radiolaria</strong>ns<br />
of Assemblage 1 and Assemblage 2 (this study); it represents the<br />
lower Rhaetian and is approximately equivalent to the Amoenum<br />
Zone. The Globolaxtorum tozeri Zone contains <strong>radiolaria</strong>ns of<br />
Assemblage 3 (this study); it represents the upper Rhaetian and is<br />
equivalent to the Crickmayi Zone.<br />
All <strong>radiolaria</strong>n species used in the zonation are discussed along<br />
with a few others having more limited occurrence. Species previously<br />
described and/or figured in the literature are discussed in terms of<br />
their occurrence in Queen Charlotte Islands. One family, five genera<br />
and 63 species are described as new.<br />
Casey, R.E. 1993. Radiolaria. In: Fossil Prokaryotes and<br />
Protists. (Lipps, J.H., Eds.). Blackwell Scientific<br />
Publications, Oxford/London. pp. 249-284.<br />
Radiolaria are marine, holoplanktic protozoans belonging to the<br />
superclass Actinopodea of the subphylum Sarcodina. The term<br />
<strong>radiolaria</strong> itself is now used informally. In the fossil record, only the<br />
class Polycystinea (or polycystine) encompassing the orders<br />
Spumellar (spurnellarians) and Nassellar (or nassellarians), which<br />
possess solid opaline skeletal structures, and the order Phaeodarea<br />
(or phaeodarians), which possess hollow skeletal structures of an<br />
admixture of silica and organic matter, are preserved. Radiolarian<br />
skeletons range in size from about 50 to 200 µm. The class<br />
Acantharea (or acantharians) are common in nearshore waters and<br />
are sometimes involved in plankton blooms, but they are never<br />
preserved as fossils. Herein, <strong>radiolaria</strong> refers to both members of<br />
the Polycystina and the Phaeodara. The polycystine <strong>radiolaria</strong>ns have<br />
the longest geologic range (Cambrian to Holocene), the widest<br />
biogeography (pole to pole, surface to abyss), and the most diverse<br />
taxonomy of the well-preserved microzooplankton. They are used<br />
extensively in biostratigraphy, in paleoceanography, and in studies<br />
on the tempo and mode of evolution. Phaeodarians may be used to<br />
infer various water and geologic conditions. The history of<br />
<strong>radiolaria</strong>n research can be separated into six periods: an early<br />
recognition of the group in both living and fossil forms; work by Ernst<br />
Haeckel; early work on living forms; a resurgence of <strong>radiolaria</strong>n work<br />
by William Riedel; <strong>radiolaria</strong>n work associated with the Deep Sea<br />
Drilling Project (DSDP) and the Ocean Drilling Program; and the<br />
current diverse modern work.<br />
Caulet, J.P., Nigrini, C. & Schneider, D.A. 1993.<br />
High resolution Pliocene-Pleistocene <strong>radiolaria</strong>n stratigraphy<br />
of the tropical Indian Ocean. Mar. Micropaleontol., 22/1-2,<br />
111-129.<br />
We refined the positions of 31 Plio-Pleistocene <strong>radiolaria</strong>n<br />
datum levels by examining 3 paleomagnetically dated cores and<br />
comparing results with 4 previously studied cores from the Central<br />
Indian Basin. When not affected by hiatuses or drastic changes in<br />
rates of sedimentation, absolute ages of <strong>radiolaria</strong>n events in<br />
multiple cores from this restricted geographic area are precise to<br />
within 0.05 million years. Some events are complicated by minor<br />
morphotypic changes at the beginning or end of ranges or within<br />
evolutionary lineages; species definitions have to be restricted
Bibliography - 1993 Radiolaria 14<br />
accordingly. Further study of these variations within an accurate<br />
chronostratigraphic framework should permit determination of the<br />
rates of these evolutionary changes.<br />
Cordey, F. & Schiarizza, P. 1993. Long-lived<br />
Panthalassic remnant: The Bridge River accretionary<br />
complex, Canadian Cordillera. Geology, 21, 263-266.<br />
Newly identified <strong>radiolaria</strong>ns from ribbon chert of the Bridge<br />
River complex in the southeastern Canadian Coast Mountains range<br />
in age from Mississippian to late Middle Jurassic. The Bridge River<br />
complex and the associated Cadwallader arc and Tyaughton and<br />
Methow basins lie between the Intermontane superterrane to the<br />
east and the Insular superterrane to the west. Triassic-Middle<br />
Jurassic development of the Bridge River subduction-accretion<br />
complex records an important component of convergence between<br />
these superterranes.<br />
The time span represented in the Bridge River complex (~170<br />
m.y.), one of the longest known age ranges for chert sedimentation,<br />
suggests that the Bridge River complex contains remnants of a longlived,<br />
potentially far-travelled Panthalassic oceanic domain.<br />
Douzen, K. & Ishiga, H. 1993. Change of paleocurrent<br />
in redox conditions of Lower Jurassic bedded cherts revealed<br />
by azimuth orientation of conical <strong>radiolaria</strong>n shells of<br />
southwest Japan. N. Osaka Micropaleont. spec. Vol., 9, 91-<br />
99. (in Japanese)<br />
Ellis, G. 1993. Late Aptian-early Albian Radiolaria of the<br />
Windalia Radiolarite (type section), Carnarvon Basin,<br />
Western Australia. Eclogae geol. Helv., 86/3, 943-995.<br />
During the Late Aptian-Early Albian Australia was inundated by<br />
a widespread (global?) marine transgression that resulted in<br />
extensive sedimentation of <strong>radiolaria</strong>n-rich facies. This facies is<br />
represented by the Windalia Radiolarite, and to a lesser extent the<br />
overlying Gearle Siltstone in the Carnarvon Basin of Western<br />
Australia. In this study, a detailed <strong>radiolaria</strong>n biostratigraphic<br />
assessment of the type section of the Windalia Radiolarite is<br />
presented. Fifty-nine <strong>radiolaria</strong>n taxa are represented, including one<br />
new genus (Windalia n. gen.) and three new species (Actinomma (?)<br />
pleiadescensis n. sp., Paronaella (?) diastimuspltere n. sp. and<br />
Praeconocaryomma excelsa n. sp.). Many of these taxa have been<br />
recorded previously from Tethyan regions. However, the<br />
assemblages are dominated in abundance by a few non-Tethyan<br />
forms which are also recognized in coeval sediments elsewhere in<br />
Australia, the Indian Ocean and the Weddell Sea. These dominant<br />
taxa are considered to be endemic elements of an "Austral" faunal<br />
realm. Many of the known biostratigraphically important <strong>radiolaria</strong><br />
are sparse or absent, but the previously recorded stratigraphic<br />
ranges of several species correspond with the Late (latest) Aptian-<br />
Early Albian age of the Windalia Radiolarite known from ammonites<br />
and belemnites, and from age constraints emplaced by the<br />
underlying and overlying formations. The published ranges of other<br />
<strong>radiolaria</strong>n species from the Windalia Radiolarite, however, conflict<br />
with this age, highlighting the limited detailed knowledge of early<br />
Cretaceous <strong>radiolaria</strong> and the difficulties in applying '"low latitude"<br />
<strong>radiolaria</strong>n biozonations to the Austral region.<br />
Feng, Q. & Liu, B. 1993a. Permian <strong>radiolaria</strong>n on<br />
southwest Yunnan. Earth Sci., J. China Univ. Geosci., 18/5,<br />
540-564.<br />
A <strong>radiolaria</strong>n fauna, consisting of 32 species belonging to 17<br />
genera, found in Laochang and Nanpan of Lancang County and<br />
Bangsha of Jinghong County, is described in this paper. The fauna<br />
can be divided into 3 assemblage zones. The sequence of these<br />
zones is listed ascendingly as follows: (1) Follicucullus assemblage<br />
zone, collected from the upper part of Laba Group in Nanpan, Late<br />
Maokou - Early Longtan. (2) Neoalbaillella optima assemblage zone,<br />
occurring in the upper part of Laba Group in Nanpan and the middle<br />
part of Laochang Formation in Laochang, Late Longtan. (3)<br />
Neoalbaillella ornithoformis assemblage zone, preserved in the upper<br />
part of Laba Group in Nanpan and the chert interbed of volcanic<br />
rocks in Bangsha, Early Changxing. The geological times of the lithostratigraphic<br />
units are discussed based on the three assemblage<br />
zones.<br />
Feng, Q. & Liu, B. 1993b. A new early Devonian<br />
<strong>radiolaria</strong>n genus from western Yunnan. Sci. China, Ser. B,<br />
36/2, 242-248.<br />
A new <strong>radiolaria</strong>n genus, Eoalbaillella belonging to Albaillellidae<br />
Deflandre emend. Holdsworth, is proposed from the Early Devonian in<br />
Western Yunnan, Southwestern China. Its test is composed of an<br />
imperforate lamellar shell and an elongate triangular framework, of<br />
which the upper part is enclosed by the lamellar shell and the lower<br />
- 96 -<br />
part, without the shell, has the shape of the letter X. The relations<br />
between new genus and other <strong>radiolaria</strong>n genera are studied and the<br />
type species of the genus is described.<br />
Fergusson, C.L., Henderson, R.A., Leitch, E.C.<br />
& Ishiga, H. 1993. Lithology and structure of the Wandilla<br />
Terrane, Gladstone-Yeppoon District, central Qeensland, and<br />
an overview of the Palaeozoic Subduction complex of the<br />
New-England fold belt. Austral. J. Earth Sci., 40/4, 403-414.<br />
The Wandilla terrane consists of, from west to east, the<br />
Doonside Formation and the Wandilla Formation. The Doonside<br />
Formation is dominated by chert and mudstone. Conodonts from a<br />
single locality (Devils Bend) indicate an age in the interval Late<br />
Silurian to Middle Devonian. The Wandilla Formation consists of<br />
mudstone with greywacke, tuff, chert and greenstone. The<br />
greywacke is dominated by volcanic detritus with sparse but<br />
persistent ooliths that suggest contemporaneity with Early<br />
Carboniferous strata of the Yarrol shelf to the west. The Wandilla<br />
terrane is structurally complex with two main deformation events.<br />
The first deformation (D1 ) formed widespread lenticular melange<br />
during offscraping at the toe of a subduction complex. The second<br />
deformation (D2 ) formed a moderately to shallowly east-dipping<br />
cleavage that typically dips less steeply than the north-northwesttrending<br />
D1 structures, and contains a down-dip elongation lineation.<br />
D2 structures were produced by the Late Permian to Triassic Hunter-<br />
Bowen Orogeny.<br />
Lithological attributes and structural styles indicate a<br />
subduction complex setting for much of the Wandilla terrane and<br />
related units farther south. New ages from chert in the subduction<br />
complex of the New England Fold Belt are mainly Early Carboniferous,<br />
consistent with a major accretionary episode in the late Early and<br />
Late Carboniferous. By analogy with the considerably better dated<br />
units of the Japanese accretionary terranes, this major period of<br />
growth may have been a result of collision of a major topographic<br />
feature with the trench (e.g. a mid-ocean ridge).<br />
Fujii, J., Hattori, I. & Nakajima, T. 1993. A study<br />
of <strong>radiolaria</strong>n biostratigraphy and magnetostratigraphy of<br />
early Mesozoic red bedded chert, central Japan. N. Osaka<br />
Micropaleont. spec. Vol., 9, 71-89. (in Japanese)<br />
Funakawa, S. 1993. Late Miocene <strong>radiolaria</strong>n fossils from<br />
eastern Hokkaido, Japan. N. Osaka Micropaleont. spec. Vol.,<br />
9, 293-311. (in Japanese)<br />
Garrison, D.L., Buck, K.R. & Gowing, M.M.<br />
1993. Winter plankton assemblage in the ice edge zone of the<br />
Weddell and Scotia Seas - composition, biomass and spatial<br />
distributions. Deep-Sea Res. Part A, oceanogr. Res. Pap.,<br />
40/2, 311-338.<br />
George, A.D. 1993. Radiolarians in offscraped seamount<br />
fragments, Aorangi range, New Zealand. New Zealand J. Geol.<br />
Geophys., 36/2, 185-199.<br />
Well-preserved <strong>radiolaria</strong>ns occur in coloured argillites at two<br />
localities in the Torlesse Terrane exposed in the Aorangi Range. The<br />
coloured argillites which host the <strong>radiolaria</strong>ns are associated with<br />
metabasite, and together these rocks are interpreted as remnants of<br />
seamounts which were dismembered immediately before or during<br />
subduction and accretion. Radiolarians from the two Aorangi Range<br />
localities are consistent with a Late Jurassic to Early Cretaceous<br />
age.<br />
Gorican, S. 1993. Jurassic and Cretaceous <strong>radiolaria</strong>n<br />
biostratigraphy and sedimentary evolution of the Budva Zone<br />
(Dinarides, Montenegro). Ph.D. Thesis. University of<br />
Lausanne, 227 p. (unpublished)<br />
The Budva Zone is the northernmost part of a long belt of<br />
Mesozoic basinal sediments, which extend southward to the Krasta-<br />
Cukali Zone in Albania and Pindos-Olonos Zone in Greece. Lowermost<br />
Jurassic to middle Cretaceous formations are defined and described.<br />
105 <strong>radiolaria</strong>n samples collected in ten sections allowed us to date<br />
pelagic sequences and to constrain ages of intervening carbonate<br />
gravity-flow deposits. Systematics of about 200 recorded<br />
<strong>radiolaria</strong>n species is discussed and supported by illustrations. For<br />
the Middle Jurassic to Turonian time interval, a local <strong>radiolaria</strong>n<br />
zonation is constructed by means of Unitary Association Method<br />
(Guex, 1977, 1991). The appearance of 138 taxa was used in the<br />
database. 48 Unitary Associations are established and grouped into<br />
15 distinct "zones". The calibration is based on the existing<br />
zonations. The Budva Zone formations are correlated to timeequivalent<br />
lithologies in the tectonically overthrusting High Karst
Radiolaria 14 Bibliography - 1993<br />
Platform. The correlation reveals a close relationship between the<br />
sedimentary and tectonic activity of the High Karst Platform margin,<br />
and facies evolution in the adjacent Budva Basin.<br />
The Hettangian to Sinemurian lime-poor "Passee Jaspeuse"<br />
Formation coincides with a subsidence of the High Karst Platform<br />
margin. In the Pliensbachian to lower Toarcian the entire basin was<br />
characterized by calcareous resediments (Lower Bar Limestone<br />
Member). The margin-ward propagation of radiolarite sedimentation<br />
(Lastva Radiolarite) and retreat of calcareous clastics (Upper Bar<br />
Limestone Member) in the Middle Jurassic are related to a<br />
development of continuous oolitic bars on the platform. The<br />
maximum expansion of radiolarites was attained in the Oxfordian and<br />
Kimmeridgian, when the platform margin was fringed by a large reefcomplex.<br />
Most of the carbonate mud in the Jurassic basinal<br />
succession was probably of platform origin. Periods of reduced<br />
periplatform-ooze supply were characterized by lime-poor to limefree<br />
basinal sedimentation. In the late Tithonian, distal sequences<br />
show a transition from siliceous to carbonate deposition (Praevalis<br />
Limestone). In the Hauterivian-Barremian, again, radiolarite<br />
sedimentation (Bijela Radiolarite) progressively replaced pelagic<br />
carbonates and persisted to the Turonian. These facies changes are<br />
correlative with synchronous shifts in the Southern Alps and<br />
Apennines. The Budva Basin, however, differs from other Tethyan<br />
basins by a lower proportion of carbonate in the Upper Jurassic and<br />
Cretaceous sequences.<br />
The composition and distributional pattern of calcareous<br />
resediments changed significantly by Late Jurassic time. Prior to<br />
that time, in the Early and Middle Jurassic, carbonate gravity-flow<br />
deposits were composed of remobilized pelagic sediments and<br />
penecontemporaneous platform debris. Contrary to this, since the<br />
Tithonian the bulk of the calcareous resediments was derived from<br />
the erosion of lithified shallow water limestones. Coarse grained<br />
turbidites became restricted to the northwestern depositional area.<br />
This facies change is believed to reflect the evolution from an<br />
extensional to a compressive regime in the internal domains of the<br />
Dinaric Tethys, which induced a differential uplift of the High Karst<br />
Platform.<br />
Gowing, M.M. 1993. Seasonal <strong>radiolaria</strong>n flux at the<br />
VERTEX Noth Pacific time-series Site. Deep-Sea Res. Part A,<br />
oceanogr. Res. Pap., 40/3, 517-545.<br />
Guex, J. 1993. Simplifications géométriques liées au stress<br />
écologique chet certain protistes. Bull. Soc. vaud. Sc. nat.,<br />
82/4, 357-368.<br />
The evolution of Silicoflagellates (Chrysophytes) is<br />
characterized by two main trends: 1.- progressive complexification<br />
of the skeleton and 2.- elongation of the skeleton with development<br />
of a bilateral symmetry and concomitant simplification of some<br />
skeletal elements (loss of the lateral radial spines). Silicoflagellates<br />
are extremely sensitive to environemental instabilities. During<br />
phases of ecological stress, the skeleton frequently shows drastic<br />
geometrical simplifications (loss of the basal ring or of the apical<br />
system), and a loss of the symmetry. The evolution of this group<br />
corroborates some hypotheses proposed in a recent paper devoted<br />
to the reversal of some evolutionary trends induced by ecological<br />
stress (GUEX,1992). A similar case of evolutionary reversal<br />
observed in <strong>radiolaria</strong>ns is briefly discussed.<br />
Haggart, J.W. & Carter, E.S. 1993. Cretaceous<br />
(Barremian-Aptian) Radiolaria from Queen Charlotte Islands,<br />
British Columbia: newly recognized faunas and stratigraphic<br />
implications. Geol. Surv. Canada, curr. res., Pap., 93-1E,<br />
55-65.<br />
Radiolarian faunas have been identified from Lower Cretaceous<br />
rocks of Queen Charlotte Islands (NTS 103B, F). Microfossils were<br />
obtained from fine grained clastic rocks of the Longarm and Haida<br />
formations and taxa indicative of the Hauterivian, Barremian, Aptian,<br />
and Albian stages were identified. The faunas include the first<br />
Cretaceous <strong>radiolaria</strong>ns noted from the northern part of the<br />
Canadian Insular Belt and the first diverse <strong>radiolaria</strong>n assemblages<br />
of Barremian and Aptian age from west coast North America. These<br />
collections are critically important in the development of a<br />
<strong>radiolaria</strong>n biochronology for the Lower Cretaceous of the North<br />
American Cordillera. The faunas demonstrate that deposition of fine<br />
clastic rocks was widespread across the Queen Charlotte Islands<br />
region during most of the Early Cretaceous and argue against<br />
diastrophism at that time.<br />
Hattori, I. 1993. Diagenetic modification of <strong>radiolaria</strong>ns<br />
in a chaotic Jurassic sedimentary sequence of the Mino<br />
Terrane, Central Japan. In: Radiolaria of giant and subgiant<br />
fields in Asia. Nazarov Memorial Volume. (Blueford, J.R. &<br />
Murchey, B.L., Eds.), Micropaleontology, special<br />
- 97 -<br />
Publication vol. 6. Micropaleontology Press, American<br />
Museum of Natural History, New York. pp. 137-152.<br />
This study documents the diagenetic modification of Middle<br />
Jurassic <strong>radiolaria</strong>ns in shale and manganese nodules which are<br />
considered to be of pelagic origin from the Tarumigawa section in the<br />
Mino Terrane, Central Japan. Based on paragenesis of authigenetic<br />
minerals, the sedimentary environment and diagenetic history of the<br />
<strong>radiolaria</strong>n-bearing rocks were analyzed. The <strong>radiolaria</strong>n<br />
assemblages in the shale differ from those in the manganese<br />
nodules. Radiolarians derived from reddish brown shale were pressed<br />
and flattened by deformation in an early stage of diagenesis. Some<br />
families of <strong>radiolaria</strong>ns were chemically and physically sensitive in<br />
diagenesis and the genus and species compositions were remarkably<br />
modified. Although multisegmented nassellarians were also<br />
deformed during the diagenesis, their characteristic shapes remain<br />
identifiable. Multisegmented nassellarians can be used as key<br />
fossils in age and paleogeographic correlation.<br />
Hattori, I., Bustillo, M.A., Arana, V. &<br />
Nishimura, A. 1993. Lepisphere and chert - microtextural<br />
comparison between two foreing Cenozoic siliceous<br />
sediments and white chert in the Nanjo Massif, Central Japan.<br />
N. Osaka Micropaleont. spec. Vol., 9 , 271-291. (in<br />
Japanese)<br />
Hollis, C.J. 1993. Latest Cretaceous to Late Paleocene<br />
<strong>radiolaria</strong>n biostratigraphy: A new zonation from the New<br />
Zealand region. In: Interrad VI. (Lazarus, D.B. & De Wever,<br />
P., Eds.), vol. 21/4. Special Issue: Marine Micropal.,<br />
Elsevier, Amsterdam. pp. 295-327.<br />
The scarcity of records of Early Paleocene <strong>radiolaria</strong>ns has<br />
meant that while <strong>radiolaria</strong>n biostratigraphy is firmly established as<br />
an important tool for correlation, there has been a long-standing gap<br />
between established zonations for the Cretaceous and from latest<br />
Paleocene to Recent. It has also led to considerable speculation over<br />
the level of faunal change across the Cretaceous/Tertiary (K/T)<br />
boundary. Consequently, the discovery of rich and diverse<br />
<strong>radiolaria</strong>n assemblages in well-delineated K/T boundary sections<br />
within siliceous limestones of the Amuri Limestone Group in eastern<br />
Marlborough, New Zealand, is of great significance for<br />
biostratigraphy and K/T boundary research. This initial report is<br />
restricted to introducing a new latest Cretaceous to mid Late<br />
Paleocene zonation based on the <strong>radiolaria</strong>n succession at four of<br />
these sections and a re-examination of faunas from coeval<br />
sediments at DSDP Site 208 (Lord Howe Rise). Three new Paleocene<br />
species are described: Amphisphaera aotea, Amphisphaera kina and<br />
Stichomitra wero. Six new interval zones are defined by the first<br />
appearances of the nominate species. In ascending order these are:<br />
Lithomelissa? hoplites Foreman (Zone RK9, Cretaceous),<br />
Amphisphaera aotea n. sp. (Zone RPI, Paleocene),<br />
Amphisphaerakinan. sp. (RP2), Stichomitra granulata<br />
Petrushevskaya (RP3), Buryella foremanae Petrushevskaya (RP4)<br />
and Buryella tetradica (RP5). Good age control from foraminifera and<br />
calcareous nannofossils permits close correlation with established<br />
microfossil zonations. Where age control is less reliable, <strong>radiolaria</strong>n<br />
events are used to substantially improve correlation between the<br />
sections. No evidence is found for mass extinction of <strong>radiolaria</strong>ns at<br />
the end of the Cretaceous. However, the K/T boundary does mark a<br />
change from nassellarian to spumellarian dominance, due to a<br />
sudden influx of actinommids, which effectively reduces the relative<br />
abundance of many Cretaceous survivors. An accompanying influx of<br />
diatoms in the basal Paleocene of Marlborough, together with<br />
evidence for an increase of total <strong>radiolaria</strong>n abundance, suggests<br />
siliceous plankton productivity increased across the K/T boundary.<br />
Possible causes for this apparently localised phenomenon are briefly<br />
discussed.<br />
Hori, R. 1993. Pantanelliidae abundance for lower Jurassic<br />
siliceous rocks. N. Osaka Micropaleont. spec. Vol., 9, 101-<br />
108. (in Japanese)<br />
Hull, D.M. 1993. Quaternary, Eocene, and Cretaceous<br />
<strong>radiolaria</strong>ns from the Hawaiian Arch, northern Equatorial<br />
Pacific Ocean. In: Proceedings of the Ocean Drilling Program,<br />
Scientific Results. (Wilkens, R.H., Firth, J., Bender, J. et al.,<br />
Eds.), vol. 136. College Station, TX (Ocean Drilling<br />
Program), pp. 3-25.<br />
Deep-sea cores recovered at Sites 842 and 843 on Leg 136 of<br />
the Ocean Drilling Program have yielded assemblages of Quaternary,<br />
Eocene, and Cretaceous <strong>radiolaria</strong>ns from the Hawaiian Arch region<br />
of the northern equatorial Pacific Ocean. Reddish-brown clays from<br />
Hole 842A (0-9.6 mbsf), Hole 842B (0-6.3 mbsf), and Hole 843C<br />
(0-4.2 mbsf) contain abundant and diverse assemblages of<br />
Quaternary <strong>radiolaria</strong>ns consisting of more than 80 species typical<br />
of the equatorial Pacific region. Quaternary <strong>radiolaria</strong>ns at these
Bibliography - 1993 Radiolaria 14<br />
sites are assignable to the Quaternary Collosphaera tuberosa<br />
Interval Zone and Amphirhopalum ypsilon Interval Zone. The boundary<br />
between these zones cannot be determined precisely because of the<br />
rarity of zonal markers below surface sediments. Correlations have<br />
been made between <strong>radiolaria</strong>n occurrences and<br />
magnetostratigraphic events elsewhere in the Pacific Ocean, but<br />
similar correlations are difficult at Sites 842 and 843 because of<br />
poor subsurface preservation. Chert samples collected from<br />
intervals in Cores 842B-10 and 842C- 1W have yielded <strong>radiolaria</strong>n<br />
ages of lower Cenomanian to Santonian and lower Cenomanian,<br />
respectively. Radiolarian assemblages in volcanic sand layers in<br />
Sections 6 and 7 of Core 842A-1H (7.5-9.6 mbsf) contain lower<br />
and middle Eocene <strong>radiolaria</strong>ns admixed with abundant Quaternary<br />
faunas. Reworked Eocene <strong>radiolaria</strong>ns appear to be restricted to thin<br />
layers of volcanic sands within the cores, suggesting deposition by<br />
turbidity currents.<br />
Hull, D.M., Pessagno, E.A.J., Hopson, C.A.,<br />
Blome, C.D. & Muñoz, I.M. 1993.<br />
Chronostratigraphic assignment of volcanopelagic strata<br />
above the coast range ophiolite. In: Mesozoic<br />
Paleogeography of the Western United States-II. (Dunn, G. &<br />
McDougall, K., Eds.), vol. 71. Pacific Section, Society of<br />
economic Paleontologists and Mineralogists, pp. 157-170.<br />
The chronostratigraphic assignments of <strong>radiolaria</strong>n cherts,<br />
tuffaceous mudstones and volcaniclastic strata (referred to herein<br />
as volcanopelagic succession) overlying the Coast Range ophiolite in<br />
the Coast Ranges of California have been refined on the basis of<br />
additional field data and recent revision of the Pessagno and others<br />
<strong>radiolaria</strong>n biostratigraphic zonation for the Middle and Upper<br />
Jurassic of North America. Revision of this zonation scheme,<br />
accomplished through the integration of <strong>radiolaria</strong>n data with<br />
ammonite biostratigraphy and geochronometry, has enabled close<br />
correlation of <strong>radiolaria</strong>n assemblages in North America, Europe, and<br />
Japan. However, major differences still exist in the stage<br />
assignments of these assemblages among different zonations. The<br />
Pessagno and others scheme is utilized herein to discuss the current<br />
chronostratigraphic assignments at five localities in the Coast<br />
Ranges: Point Sal, Stanley Mountain, Cuesta Ridge, and Llanada in the<br />
southern Coast Ranges, and Black Mountain (Geyser Peak area) in<br />
the northern Coast Ranges of California. Stage assignments for<br />
volcanopelagic successions in these areas range from uppermost<br />
Callovian/lower Oxfordian to upper Tithonian.<br />
Iijima, H., Sekine, K. & Saito, Y. 1993. Jurassic<br />
<strong>radiolaria</strong>ns from the Clastic Rock Unit of the northern part<br />
of the Chichibu Belt in the Kanto Mountains, central Japan.<br />
Bull. nat. Sci. Mus., Tokyo, Ser. C, 19/3, 81-89.<br />
Imazato, A. & Otoh, S. 1993. Jurassic <strong>radiolaria</strong>ns from<br />
the Nyukawa area, northernmost part of the Mino Belt. N.<br />
Osaka Micropaleont. spec. Vol., 9, 131-141. (in Japanese)<br />
Ishiga, H. 1993. Carbonaceous mudstones of the lower<br />
Toarcian (Jurassic) and the Permian/Triassic boundary<br />
horizons in Japan. N. Osaka Micropaleont. spec. Vol., 9, 51-<br />
69.<br />
Jafri, S.H., Balaram, V. & Govil, P.K. 1993.<br />
Depositional environments of Cretaceous <strong>radiolaria</strong>n cherts<br />
from Andaman-Nicobar Islands, northeastern Indian Ocean.<br />
Marine Geol., 112/1-4, 291-301.<br />
Radiolarian cherts of Cretaceous age are tectonically<br />
associated with pillow basalts, ultramafic rocks and turbidites in the<br />
outer sedimentary arc of the Andaman-Nicobar Islands. These<br />
<strong>radiolaria</strong>n cherts are composed of <strong>radiolaria</strong>n tests, quartz, albitic<br />
feldspar, basaltic rock fragments, montmorillonite and chlorite, and<br />
are classified into three different types: (I) massive tuffaceous<br />
<strong>radiolaria</strong>n claystone, (II) bedded tuffaceous <strong>radiolaria</strong>n claystone,<br />
and (III) bedded <strong>radiolaria</strong>n argillaceous chert. Radiolarian cherts of<br />
Types I and II are similar in composition, characterised by the lower<br />
abundance of SiO2 , total REE (Σ REE) and are rich in Fe203 , MgO, TiO2 and Al203 and trace elements (e.g., Ni, Co, Cr, V, Rb, Sr, Cu and Zr)<br />
as compared to those of Type 111 <strong>radiolaria</strong>n chert. Based on<br />
elemental abundance as well as petrological evidence, it is<br />
suggested that both Types I and 1I cherts have been derived from a<br />
mixed continental and basaltic source. In comparison, Type III chert<br />
seems to have been derived from a continental source.<br />
Low values of Fe20 3 /AI20 3 , Σ REE and weakly positive to<br />
negative Ce anomalies in Types I and II cherts further suggest that<br />
they accumulated close to continental margins as compared to Type<br />
III chert, which is suggested to have accumulated in a relatively<br />
distal oceanic (hemipelagic) environment. It is inferred that these<br />
<strong>radiolaria</strong>n chert sequences, which were originally deposited in<br />
- 98 -<br />
different oceanic environments, were scraped off the subducting<br />
Indian plate, became tectonically juxtaposed, and now constitute a<br />
part of the Andaman-Nicobar ophiolite complex.<br />
Kashima, N. 1993. Discovery of <strong>radiolaria</strong>n fossils from<br />
the Hokezu Block at the Northern area of Uwajima, Shikoku.<br />
N. Osaka Micropaleont. spec. Vol., 9 , 225-231. (in<br />
Japanese)<br />
Kashiwagi, K. & Yao, A. 1993. Jurassic to Early<br />
Cretaceous <strong>radiolaria</strong>ns from Yuasa area in western Kii<br />
Peninsula, southwest Japan and its significance. N. Osaka<br />
Micropaleont. spec. Vol., 9, 177-189. (in Japanese)<br />
Kawabata, K. & Ito, N. 1993. Early Jurassic <strong>radiolaria</strong>ns<br />
from northernmost part of the Ashio Terrane, Niigata<br />
Prefecture, central Japan. N. Osaka Micropaleont. spec. Vol.,<br />
9, 119-129. (in Japanese)<br />
Kimura, K. 1993. Occurrence of siliceous claystone and<br />
associated greenstones in the Mino-Tamba Belt. Bull. geol.<br />
Surv. Japan, 44/12, 727-743. (in Japanese)<br />
Kozlova, G.E. 1993. Radiolarian zonal scale of the boreal<br />
Paleogene. In: Radiolaria of giant and subgiant fields in Asia.<br />
Nazarov Memorial Volume. (Blueford, J.R. & Murchey, B.L.,<br />
Eds.), Micropaleontology, special Publication vol. 6.<br />
Micropaleontology Press, American Museum of Natural<br />
History, New York. pp. 90-93.<br />
Boreal Paleogene <strong>radiolaria</strong>ns of middle Eurasia occur in many<br />
areas including West Siberia, the Urals, the North Caspian<br />
depression, Turgay. the Basin of the Volga River, the Don River and<br />
the Dnieper River. Thirteen Paleogene successive <strong>radiolaria</strong>n<br />
assemblages are recognized. each consisting of 7-80 species.<br />
These assemblages contain species characteristic of the boreal<br />
realm and those typical of tropical and subtropical basins including<br />
some <strong>radiolaria</strong>n index species of the Atlantic. At some stratigraphic<br />
levels, tropical species account for 20-85% of an assemblage. The<br />
age of the <strong>radiolaria</strong>n assemblages can be correlated using<br />
planktonic foraminifers in the North Caspian depression. This article<br />
reviews the <strong>radiolaria</strong>n zonation currently used by Russian workers.<br />
Kozur, H. 1993a. First evidence of Liassic in the Vicinity<br />
of Csovár (Hungary) and its Paleogeographic and<br />
Paleotectonic Significance. Jb. geol. Bundesanst. (Wien),<br />
136/1, 89-98.<br />
The Csovar Limestone Formation sensu HAAS & KOVACS<br />
(1985) consists of two units different in lithofacies and age. The<br />
lower unit (Csovar Limestone Formation sensu BALOGH, 1981, who<br />
established this formation) consists of dark, bituminous, often<br />
resedimented and graded limestones, cherty limestones, marly<br />
limestones and marls. The surface outcrops of the Csovar Limestone<br />
Formation belong to the Upper Rhaetian. In a borehole also Norian is<br />
present in the Csovar Limestone Formation. The upper unit consists<br />
of bedded, in some parts massive, light-yellowish to light-brownish<br />
micritic limestones and cherty limestones. The upper part contains<br />
thick slump breccias. The upper unit is separated from the Csovar<br />
Limestone Formation s.l. and designated as Varhegy Cherty<br />
Limestone Formation. Its largest part belongs to the Hettangian. The<br />
basal Varhegy Cherty Limestone Formation has yielded<br />
Neohindeodella detrei KOZUR & MOCK, the stratigraphically<br />
youngest conodont species of the world that characterizes probably<br />
the basal Hettangian. The uppermost part of the Varhegy Cherty<br />
Limestone Formation belongs to the Sinemurian.<br />
Kozur, H. 1993b. Upper Permian Radiolarians from the<br />
Sosio Valley Area, Western Sicily (Italy) and from the<br />
Uppermost Lamar Limestone of West Texas. Jb. geol.<br />
Bundesanst. (Wien), 136/1, 99-123.<br />
Red deep-water clays from the Sosio Valley area in Western<br />
Sicily contain one of the richest Upper Permian <strong>radiolaria</strong>n faunas of<br />
the world. 4 new genera and 4 new species are described from this<br />
fauna. Conodonts from a calcarenite intercalation near to the richest<br />
<strong>radiolaria</strong>n-bearing sample indicate a Dzhulfian age. The<br />
stratigraphic and paleogeographic importance of this deep-water<br />
<strong>radiolaria</strong>n is discussed. For comparison with the Sicilian Upper<br />
Permian <strong>radiolaria</strong>n fauna, the <strong>radiolaria</strong>n fauna of the uppermost<br />
Lamar Limestone of West Texas was re-investigated. In contrast to<br />
the previous age determinations this fauna is not of Late Capitanian,<br />
but of Dzhulfian age. Follicullus bispinosum n. sp. has been<br />
described from this fauna
Radiolaria 14 Bibliography - 1993<br />
Kozur, H. & Mostler, H. 1993. Anisian to Middle<br />
Carnian <strong>radiolaria</strong>n zonation and description of some<br />
stratigraphically important <strong>radiolaria</strong>ns. Geol. Pälont. Mitt.<br />
Innsbruck, Sonderbd., 3, 39-199.<br />
Kruglikova, S.B. 1993. Observations on the distribution<br />
of polycystine Radiolaria in marine sediments (mainly at<br />
high taxonomic levels). In: Radiolaria of giant and subgiant<br />
fields in Asia. Nazarov Memorial Volume. (Blueford, J.R. &<br />
Murchey, B.L., Eds.), Micropaleontology, special<br />
Publication vol. 6. Micropaleontology Press, American<br />
Museum of Natural History, New York. pp. 17-21.<br />
Data on the ecology and distribution of modem <strong>radiolaria</strong>n<br />
species and higher taxonomic classification is poor. This paper<br />
reviews published data on the diversity of polycystine <strong>radiolaria</strong>n<br />
assemblages in different regions of the world's ocean and looks at<br />
the ecological distribution of high rank taxa.<br />
Kurimoto, C., Teraoka, Y. & Okamura, K. 1993.<br />
Cretaceous <strong>radiolaria</strong>ns from the Shimanto Belt of the Saiki<br />
area, Kyushu. N. Osaka Micropaleont. spec. Vol., 9, 233-<br />
247. (in Japanese)<br />
Kuwahara, K. 1993. Morphological change of late<br />
Permian Radiolaria Albaillella. N. Osaka Micropaleont. spec.<br />
Vol., 9, 35-40. (in Japanese)<br />
Lipman, R.K. 1993. Paleogene Radiolaria of North Eurasia<br />
and their implication for a global correlation. In: Radiolaria<br />
of giant and subgiant fields in Asia. Nazarov Memorial<br />
Volume. (Blueford, J.R. & Murchey, B.L., Eds.),<br />
Micropaleontology, special Publication vol. 6 .<br />
Micropaleontology Press, American Museum of Natural<br />
History, New York. pp. 94-97.<br />
Radiolarians can be useful in developing a global zonal<br />
stratigraphy of Paleogene marine deposits. In Paleogene deposits<br />
approximately 100 species of <strong>radiolaria</strong>ns are found that can be<br />
used to correlate strata from North Eurasia to other continents and<br />
other oceanic sediments. A correlation scheme of zonal division of<br />
Paleogene of the North Eurasia and oceanic troughs based on<br />
<strong>radiolaria</strong>ns is given and their correlation with zones based on<br />
foraminifers and nannoplankton. This article reviews the Paleogene<br />
<strong>radiolaria</strong>n stratigraphy used by Soviet researchers prior to 1990.<br />
Lipps, J.H. 1993. Fossil Prokaryotes and Protists. ,<br />
Blackwell Scientific Publications Oxford, 342 p.<br />
Fossil Prokaryotes and Protists is a textbook for an advanced<br />
paleontology course dealing with the morphology, systematics,<br />
distribution in time and space, and evolution of single-celled<br />
organisms, as represented in the fossil record. The book assumes a<br />
knowledge of the principles of paleontology or general biology, and<br />
students would be well advised to have taken an introductory course<br />
in paleontology, biology, botany, or zoology before using this book.<br />
No preceding course on systematic paleontology is necessary,<br />
because each group considered here is unique and unlike any of the<br />
multicellular animals or plants. An understanding of basic geology<br />
will be useful, although separate sections on biostratigraphy,<br />
paleoceanography, and paleoenvironments are included because that<br />
is the chief geologic use of most unicellular fossils.<br />
Traditionally, fossils of protists, although not usually those of<br />
prokaryotes, have been taught in courses called micropaleontology,<br />
but just as traditionally, these courses have covered any tiny fossils<br />
that require a microscope for study, including those of many<br />
invertebrate, vertebrate, and plant groups. Tiny fossils of higher<br />
plants, invertebrates, and vertebrates are excluded from this<br />
textbook in order to treat levels of biologic organization together<br />
rather than a particular technique of study. Both approaches have<br />
merit. Microfossils are found together in the same samples<br />
regardless of biologic origin, and the inclusion of the common fossils<br />
likely to be encountered in microscopic examination of samples in a<br />
single text book has some practical value. However, modern<br />
techniques for study of the very wide variety of microfossils are no<br />
longer simple, and nearly every group now requires special<br />
techniques. In addition, paleontology in general is making great<br />
advances by moving towards a more biologic interpretation of<br />
fossils, so textbook treatments of fossils should be usefully<br />
organized by systematic affinities. Fossil Prokaryotes and Protists<br />
does just that by including bacteria and single-celled algae and<br />
protozoa in a single volume. The multicellular invertebrate<br />
microfossils are considered in the companion textbook to this<br />
volume, Fossil Invertebrates, edited by Richard S. Board man, Alan H.<br />
Cheetham, and Albert J. Rowell, and also published by Blackwell<br />
- 99 -<br />
Scientific Publications in 1987. Vertebrate and plant fossils are<br />
considered in any of several modern textbooks.<br />
Some topics in the general field of paleontology have not yet<br />
had major impact on the study of fossil prokaryotes and protists.<br />
Cladistic analysis, for example, has not been applied to unicellular<br />
fossils in any major way, although the method is discussed in this<br />
book with the hope that it will be more widely applied by the next<br />
generation of protistan paleontologists. Molecular phylogeny has<br />
clarified relationships between large groups of prokaryotes and<br />
between some protists and other kingdoms, but these techniques<br />
have not been applied extensively enough to reveal information<br />
useful in the context of this book. So many of the more recent<br />
advances in general paleontology and evolutionary biology have<br />
great but unrealized potential in prokaryotic and protistan<br />
paleontology. Other entire fields are based solidly on unicellular<br />
fossils; for example, paleoceanography. While such topics are useful<br />
in a textbook on these fossils, in recent years they have grown so<br />
much that they too deserve and have textbooks and courses devoted<br />
exclusively to them. The specific goals, then, of Fossil Prokaryotes<br />
and Protists are:<br />
1 to provide an understanding of the fossil record of unicellular<br />
organisms;<br />
2 to provide an understanding of the important role these<br />
organisms have played in Earth and life history;<br />
3 to provide an understanding of the usefulness of these<br />
fossils in solving certain geologic problems;<br />
4 to include enough information about the biology, morphology,<br />
and relationships of prokaryote and protist fossils to enable<br />
students to enter the professional literature, to be conversant with<br />
specialists on each group, or to proceed to more advanced studies of<br />
these groups;<br />
5 to provide a summary of the morphology, systematic<br />
paleontology, biology, and paleontology of unicellular fossils<br />
sufficiently detailed that advanced students can recognize and<br />
develop geologic or biologic research problems in their own programs<br />
that can be addressed using these fossils, given advice from their<br />
professors about topics amenable to study at their institutions.<br />
The book is organized into two parts—one dealing with general<br />
aspects of fossil unicellular organisms, and another describing each<br />
major group. Fossil prokaryotes first appear in the fossil record 3.5<br />
billion years ago (Ga), and so they are close to the very origin of life<br />
on Earth. A single, brief chapter is included on the origin of life,<br />
constrained by reasonable geologic and biochemical evidence, in<br />
order to provide an understanding of how the first unicellular fossils<br />
themselves may have arisen. Another chapter deals with the<br />
problems peculiar to single-celled fossils, and a third covers their<br />
applications to geologic problems because protists play an essential<br />
role in modern geology. A brief evolutionary history of the<br />
prokaryotes and protists and their role in influencing Earth's history<br />
provides a summary in which to place succeeding chapters that deal<br />
with specific groups of organisms.<br />
The 11 major unicellular contributors to the fossil record are<br />
considered in detail in the second part, each written by practising<br />
experts. One or two groups that occur very sparsely in the fossil<br />
record, for example thecamoebians, are omitted. The chapters are<br />
organized similarly: an introduction, history of study, morphology<br />
and systematics, biology, paleobiology, biostratigraphy, and an<br />
evolutionary history of the group. The level of systematic treatment<br />
of each group varies depending on its diversity and complexity. All<br />
chapters include a short list of supplementary reading that can<br />
provide additional information for the students or instructor. The<br />
paleontology of unicellular organisms has grown so much in the past<br />
few decades that no individual can adequately deal with all groups.<br />
Well over 40000 technical papers have appeared on aspects of<br />
single-celled fossils in the last two decades alone. Multiauthored<br />
texts are now standard. This approach has the particular problem<br />
that chapters vary in treatment and style. Partly that cannot be<br />
avoided because each expert has made his or her own judgement<br />
about what material should be included within the objectives and<br />
outline for each chapter, and each has their own style. Even more<br />
important in this book, however, is that each group is quite variable<br />
in its complexity, its geologic or ecologic distribution, and in the<br />
knowledge accumulated about it. For example, foraminifera have<br />
been studied carefully for more than 150 years, have over 60000<br />
described benthic and planktic species, have perhaps as many as<br />
6000 workers in industrial and research institutions worldwide,<br />
range in age from Cambrian to Recent, and live in environments from<br />
fresh water to shallow water of all types, to the deep sea, and from<br />
polar to equatorial regions. Silicoflagellates, in contrast, have been<br />
intensively studied for less than 30 years, have a few hundred<br />
species at most, have a dozen or so workers worldwide, are wholly<br />
planktic in the surficial waters of the oceans, and range in age from<br />
the Cretaceous to the Recent. Naturally, foraminifera will be treated<br />
less inclusively than silicoflagellates, although more pages will be<br />
devoted to them. Such is the nature of paleontology.
Bibliography - 1993 Radiolaria 14<br />
Each chapter has been reviewed by other experts in the field,<br />
and the entire book has been reviewed by paleontologists who teach<br />
this subject. Nevertheless, the book will surely differ in various<br />
respects from most courses. It is the only textbook that treats<br />
single-celled fossils exclusively and that includes all the major<br />
groups. The editor alone is responsible for this organization, and he<br />
hopes that the book marks the initiation of a more unified biologic<br />
approach to systematic paleontology in general.<br />
Maate, A., Martin-Algarra, A., O'Dogherty, L.,<br />
Sandoval, J. & Baumgartner, P.O. 1993. Découverte<br />
du Dogger dans la Dorsale calcaire interne au Sud de Tetouan<br />
(Rif septentrional, Maroc). Conséquences<br />
paléogéographiques. C.R. Acad. Sci. (Paris), Sér. II, 317/2,<br />
227-233.<br />
The Dogger (Bajocian-Lower Bathonian) has been dated for the<br />
first time in the internal Limestone Dorsale of the Rif by means of<br />
ammonites and <strong>radiolaria</strong>ns. It shows <strong>radiolaria</strong>n and nodular<br />
limestone facies. It is concluded, then, that <strong>radiolaria</strong>n<br />
sedimentation began during the Dogger in this realm, and that a<br />
drowning of the "Ghomaride margin" occurred at that time.<br />
Marsella, E., Kozur, H. & D'Argenio, B. 1993.<br />
Monte Facito Formation (Scythian-Middle Carnian). A<br />
deposit of the ancestral Lagonegro Basin in the Southern<br />
Apennines. Boll. Serv. geol. Ital., 110, 225-248.<br />
The sedimentary sequence of the Lagonegro Domain is among<br />
the most important rock assemblages in the structural pattern of<br />
Southern Italy. Rocks considered to be part of such domain form a<br />
pile of imbricates well developed in the median part of the Southern<br />
Apennines. A composite sequence ranging in age from Triassic to<br />
Neogene and showing a variety of facies related to a deep water<br />
basin, was restored by previous Authors. We report here a study of<br />
several sections of the lower part of the Lagonegro sequence in the<br />
northern area of outcrop which allowed to distinguish three main<br />
intervals: a Lower Clastic Interval (higher Middle Scythian to basal<br />
Anisian), an Olistostromic Interval (Late Ladinian to Early Carnian)<br />
and a Pelagic Limestone-Marl Interval (Anisian to Middle Carnian).<br />
Matsuda, S. & Ogawa, Y. 1993. Two-stage model of<br />
incorporation of seamount and oceanic blocks into<br />
sedimentary melange: geochemical and biostratigraphic<br />
constraints in Jurassic Chichibu accretionary complex,<br />
Shikoku, Japan. Island Arc, 2/1, 7-14.<br />
Matsuoka, A. 1993a. Localities and biostratigraphy of<br />
Jurassic Radiolaria in Japan. In: Radiolaria of giant and<br />
subgiant fields in Asia. Nazarov Memorial Volume. (Blueford,<br />
J.R. & Murchey, B.L., Eds.), Micropaleontology, special<br />
Publication vol. 6. Micropaleontology Press, American<br />
Museum of Natural History, New York. pp. 153-160.<br />
More than 140 <strong>radiolaria</strong>n species have been recently<br />
described from pelagic <strong>radiolaria</strong>n chert (mainly Lower Jurassic),<br />
hemipelagic siliceous mudstone (mainly Middle Jurassic) and<br />
terrigenous mudstone (Middle-Upper Jurassic) in the Mino and the<br />
southem Chichibu Terranes of southwest Japan and from pelagic<br />
<strong>radiolaria</strong>n chert (uppermost Jurassic) in the Sorachi-Yezo Terrane<br />
of northeast Japan. Their type localities are shown and their relative<br />
biostratigraphic positions are placed in the framework of Jurassic<br />
<strong>radiolaria</strong>n zonation of Japan, which consists of the Parahsuum<br />
ovale, Archicapsa pachyderma, Laxtorum(?) jurassicum,<br />
Tricolocapsa plicarum, Tricolocapsa conexa, Stylocapsa(?) spiralis,<br />
Cinguloturris carpatica and Pseudodictyomitra primitiva Zones in<br />
ascending order.<br />
Matsuoka, A. 1993b. Living <strong>radiolaria</strong>ns around the<br />
Sesoko Island Okinawa Prefecture. Fossils, 54, 1-9. (in<br />
Japanese)<br />
Living <strong>radiolaria</strong>ns were collected from the surface water<br />
around the Sesoko Island by using a plankton net. The fauna is<br />
composed of more than 30 species. The dominant species are<br />
Didymocyrtis tetrathalamus tetrathalamus, Euchitonia elegans,<br />
Tetrapyle octacantha, Pterocanium praetextum praetextum,<br />
Pterocorys zancleus. This paper documents the result of light<br />
microscopic observation of the following nine species; Dictyocoryne<br />
profunda, Dictyocoryne truncatum, Euchitonia elegans, Lophophaena<br />
hispida, Eucyrtidium hexastichum, Pterocanium praetextum<br />
praetextum, Carpocanistrum coronatum, Acanthodesmia vinculata,<br />
Zygocircus productus.<br />
- 100 -<br />
Matsuoka, A. 1993c. Observation of living <strong>radiolaria</strong>ns<br />
from the surface water in the Caribbean Sea. N. Osaka<br />
Micropaleont. spec. Vol., 9, 349-363. (in Japanese)<br />
Miyamoto, T. & Kuwazuru, J. 1993. Finding of Early<br />
Jurassic Radiolarians from the Hashirimizu formation at the<br />
Hikawa Valley, Kumamoto Prefecture, Kyushu and its<br />
geological significance. N. Osaka Micropaleont. spec. Vol.,<br />
9, 165-175.<br />
Miyamoto, T. & Tanimoto, Y. 1993. Late Permian<br />
olistostromes Kamoshishigawa formation in the Chichibu<br />
Belt of south Kyushu, southwest Japan. N. Osaka<br />
Micropaleont. spec. Vol., 9, 19-33.<br />
Moore, T.C., Shackleton, N.J. & Pisias, N.G.<br />
1993. Paleoceanography and the diachrony of <strong>radiolaria</strong>n<br />
events in the eastern Equatorial Pacific. Paleoceanography,<br />
8/5, 567-586.<br />
The development of an orbitally tuned time scale for the ODP<br />
leg 138 sites provides biostrstigraphers a very high resolution<br />
chronostratigraphic framework. With this framework we are better<br />
able to define which of the first and last appearances of species<br />
appear to be synchronous. In addition, the geographic distribution of<br />
sites provides the means with which the detailed spatial patterns of<br />
invasion of new species and the extinction of older species can be<br />
mapped. These maps not only provide information on the process of<br />
evolution migration, and extinction, they can also be related to water<br />
mass distributions and near-surface circulation of the ocean. Of 39<br />
<strong>radiolaria</strong>n events studied at 11 sites in the eastern equatorial<br />
Pacific, 28 were found to have a minimum range in their estimated<br />
age that exceeded 0.15 m.y. The temporal pattern of first and last<br />
appearances of these diachronous events have coherent spatial<br />
patterns that indicate shifts in the areas of high oceanographic<br />
gradients over the past 10 Ma. These changes in the locations of<br />
high gradient regions suggest that the South Equatorial Current<br />
(SEC) was north of its present position prior to approximately 7 Ma.<br />
There was a southward shift in the northern boundary of this current<br />
between approximately 6 and 7 Ma, and the development of a<br />
relatively strong gradient between the northeastern and<br />
northwestern sites. Between approximately 3.7 and 3.4 Ma, there<br />
was a very slight northward shift in the northern boundary of the SEC<br />
and the steep gradients between the northeastern and northwestern<br />
sites may have disappeared. This change is thought to be associated<br />
with the closing of the isthmus of Panama. The temporal-spatial<br />
patterns of diachronous events younger than 3.4 Ma are consistent<br />
with patterns of circulation in the modern ocean.<br />
Mostler, H. & Krainer, K. 1993. Saturnalidae<br />
radiolarien aus dem Langobard der südalpinen karawanken<br />
(Kärnten, Österreich). Geol. Pälont. Mitt. Innsbruck, 19, 93-<br />
131.<br />
In the Langobardian of the southalpine Karawanken Mountains<br />
(Carinthia, southern Austria) a surprisingly rich fauna of saturnalid<br />
<strong>radiolaria</strong>ns has been observed, allowing a stratigraphic subdivision<br />
of the investigated sequence of the Buchenstein Formation.<br />
Whereas during the Fassanian no saturnalid <strong>radiolaria</strong>ns<br />
appear, the first representatives of this group have been already<br />
recorded from the Lower Langobardian of Hungary. Immediately after<br />
that, during the Langobardian II (mungoensis-Zone), an explosive<br />
evolution of saturnalid <strong>radiolaria</strong>ns belonging to the Entactinara<br />
started. In the lower part of the Langobardian II 4 genera with 28<br />
species were already present.<br />
Based only on genera it is possible to divide the <strong>radiolaria</strong>n<br />
fauna, which stratigraphically belongs to the Muelleritortus<br />
cochleata-Zone, into two clearly discernible faunas. Based on<br />
species a threefold division is possible. Saturnalid <strong>radiolaria</strong>ns<br />
belonging to the Spumellaria are absent in the Langobardian, they<br />
first occur in the Cordevolian with 3 genera.<br />
Whereas representatives of the genus Austrisaturnalis occur<br />
from the Langobardian II up to the Cordevolian, Praeheliostaurus<br />
first seems to appear in the Cordevolian.<br />
Altogehter, for the Langobardian II and Cordevolian 2 new<br />
families, 4 new genera and 26 new species of saturnalid <strong>radiolaria</strong>ns<br />
are described. According to the <strong>radiolaria</strong>n fauna, the Buchenstein<br />
Formation of the southalpine Karawanken Mountains ranges in age<br />
from the Upper Fassanian (Oertlispongus primitivus - Subzone) up to<br />
the uppermost Langobardian II (Muelleritortus cochleata-Zone).<br />
Motoyama, I. 1993. Late Miocene and Pliocene<br />
<strong>radiolaria</strong>n datum levels from DSDP Sites 192 and 302, and
Radiolaria 14 Bibliography - 1993<br />
Hole 438A of the mid- to high-latitutde NW Pacific. N. Osaka<br />
Micropaleont. spec. Vol., 9, 337-347. (in Japanese)<br />
Nagai, H. & Mizutani, S. 1993. Early Triassic<br />
<strong>radiolaria</strong>ns from Tsuzuya, Minokamo City, Gifu Prefecture,<br />
central Japan. Bull. Nagoya Univ. Furukawa Mus., 9, 1-23.<br />
(in Japanese)<br />
Early Triassic <strong>radiolaria</strong>ns extracted from bedded chert<br />
exposed at Tsuzuya (Minokamo City, Gifu Prefecture) in the Mino<br />
terrane are briefly described. They are partly correlative with those<br />
of the Parentactinia nakatsugawaensis (Pn) assemblage of Sugiyama<br />
(1992) and are supposed to be Spathian in age. In the study area,<br />
this Spathian part of chert seems to be successively overlain by the<br />
Anisian and younger chert; but no older or lower part is exposed. The<br />
chert formation changes abruptly to sandstone of the clastic facies<br />
to an apparently lower direction. The occurrence of the Spathian<br />
<strong>radiolaria</strong>ns in this area suggests that the early Triassic bedded<br />
chert is rather common as has been pointed out so far by the<br />
paleontological evidence of conodont. The Triassic chert formation in<br />
the Mino terrane is discussed from the <strong>radiolaria</strong>n biostratigraphic<br />
point of view.<br />
Nazarov, B.B. & Ormiston, A.R. 1993. New<br />
biostratigraphically important Paleozoic Radiolaria of<br />
Eurasia and North America. In: Radiolaria of giant and<br />
subgiant fields in Asia. Nazarov Memorial Volume. (Blueford,<br />
J.R. & Murchey, B.L., Eds.), Micropaleontology, special<br />
Publication vol. 6. Micropaleontology Press, American<br />
Museum of Natural History, New York. pp. 22-60.<br />
In previous publications by the authors (Nazarov and Ormiston<br />
1985a, 1985b, 1986). a scheme for the temporal succession and<br />
distribution of twenty-seven <strong>radiolaria</strong>n assemblages (Cambrian to<br />
Permian) was introduced as a means for biostratigraphic subdivision<br />
of the Paleozoic using <strong>radiolaria</strong>ns. Among the component species of<br />
these assemblages, <strong>radiolaria</strong>ns of the Late Carboniferous to<br />
Permian are more completely described, whereas older ones remain<br />
insufficiently characterized. There are many <strong>radiolaria</strong>n species<br />
from the Ordovician to Middle Carboniferous which have<br />
biostratigraphic importance but have not been described. To fill that<br />
need, two new genera, Haplotaeniatum, and Aciferopylorum, and<br />
thirty-three new species are described, and four species are<br />
redescribed from the lower and middle Paleozoic. In addition, four<br />
new polycystine species are described from the Lower Permian of<br />
the southern Urals and western Texas. The diagnosis of Meschedea<br />
(Won 1983) is modified and augmented. Range charts are provided<br />
for Ordovician, Silurian, Devonian, Mississippian and latest<br />
Carboniferous to earliest Permian <strong>radiolaria</strong>ns.<br />
Nishimura, A. 1993. Nazarov, Boris B. (1988): Paleozoic<br />
Radiolaria. Practical manual of microfauna of the USSR,<br />
Leningrad "Nedra" vol. 2, 232p. N. Osaka Micropaleont.<br />
spec. Vol., 9, 365-377. (in Japanese)<br />
Nishimura, H., Kawata, T. & Ogawa, Y. 1993.<br />
Microfabrics of Deep Sea Bottom Sediment Collected by<br />
Research Dive 134 of "Shinkai 6500". Proc. JAMSTEC<br />
Symp. Deep Sea Res., 9, 49-64. (in Japanese)<br />
Deep sea bottom and fissure sediment was sampled by<br />
Research Dive 134 of "Shinkai 6500" in the oceanward slope of the<br />
Japan trench. The primary objective of the study was to examine the<br />
contents of three samples of Recent biogenic sediment with a<br />
scanning electron microscope. Our observation clarified that the<br />
samples consist mainly of Recent diatom shells, Tertiary and Recent<br />
<strong>radiolaria</strong>ns, silicoflagellates, foraminifers and Tertiary coccoliths,<br />
sponge spicules, and clay minerals. The geological age indicated by<br />
fossils, the state of preservation, arrangements of Recent shells and<br />
spicules, and composition of their fillings, suggest that flocculated<br />
solitary planktonic shells and colonial phyto- and zoo-planktons sank<br />
from the oceanic surface layer and accumulated on the bottom at<br />
the same time as the arrival of derived Tertiary and Recent<br />
sediment.<br />
The secondary objective was to classify the microfabrics in<br />
three core samples. An approach to microfabric characterization<br />
based on the size of grains and particles, arrangement of grains and<br />
assemblages, and size and form of pore-spaces has been presented<br />
to accommodate the depositional environments in the deep sea and<br />
the relationship between diagenetic effect (especially compaction)<br />
and depth in bottom sediment.<br />
Ogawa, Y. 1993. Destruction and dissolution of <strong>radiolaria</strong>n<br />
test in relation to the present and ancient decollement zones,<br />
Barbados accretionary compley, Ocean Drilling Program Leg<br />
- 101 -<br />
110. Sci. Rep. Inst. Geosci., Univ. Tsukuba, Sect. B: geol.<br />
Sci., 14, 53-64.<br />
Radiolarian preservation states related to mechanical<br />
destruction and chemical dissolution of samples from Ocean Drilling<br />
Program Leg 1 10, the Barbados accretionary complex. are observed<br />
by using SEM photographs, and are classified into four grades. The<br />
first is almost intact, and the second is structurally fragmented. The<br />
latter group results from slight shearing in the imbricate thrust part<br />
or in the deeper part in front of the deformation front. The third<br />
preservation grade is defined by chemical dissolution chiefly<br />
observed near the thrust faults or along the decollement zone. The<br />
fourth grade is of strong shearing characterized by striated<br />
foliation. This is only seen in samples of the present and plausible<br />
ancient decollement zones. The ancient decollement zone is<br />
interpreted to be uplifted in the accretionary complex by<br />
underplating.<br />
Okamoto, S. 1993. Radiolarian fossils obtained from the<br />
Cretaceous Miyama Complex of the Shimanto Belt in the<br />
western part of the Kii Peninsula. N. Osaka Micropaleont.<br />
spec. Vol., 9, 205-214. (in Japanese)<br />
Ondrejickowa, A., Borza, V., Korabova, K. &<br />
Michalik, J. 1993. Calpionellid, <strong>radiolaria</strong>n and<br />
calcareous nannoplankton association near the Jurassic-<br />
Cretaceous boundary (Hrusove section, Cachticke Karpaty<br />
Mts., western Carpathians). Geologica carpath., 44/3, 177-<br />
188.<br />
The article presents the results of a biostratigraphic study<br />
based on the distribution and joint occurrences of calpionellids,<br />
<strong>radiolaria</strong>ns and calcareous nannoplankton, in a time section around<br />
the Jurassic-Cretaceous boundary in the Hrusove section of the<br />
Cachticke Karpaty Mts. The results gained show that the boundaries<br />
of biozones established on the basis of studies of the above<br />
mentioned groups of micro- and nannoplankton are not<br />
synchronnous. The association of <strong>radiolaria</strong>ns (U.A.11) and<br />
calcareous nannoplankton (zonee CC1 Nannoconus steinmanii<br />
occurs in the uppermost Tithonian, below the boundary of the<br />
calpionellid zones Crasicolaria/Calpionella, which in the conception<br />
of Remane et al. (1986) corresponds to the Tithonian-Berriasian<br />
boundary.<br />
Ormiston, A.R. 1993a. Dedication: Dr. Boris Borisovich<br />
Nazarov (1937-1989). In: Radiolaria of giant and subgiant<br />
fields in Asia. Nazarov Memorial Volume. (Blueford, J.R. &<br />
Murchey, B.L., Eds.), Micropaleontology, special<br />
Publication vol. 6. Micropaleontology Press, American<br />
Museum of Natural History, New York. pp. 1-2.<br />
Ormiston, A.R. 1993b. The association of <strong>radiolaria</strong>ns<br />
with hydrocarbon source rocks. In: Radiolaria of giant and<br />
subgiant fields in Asia. Nazarov Memorial Volume. (Blueford,<br />
J.R. & Murchey, B.L., Eds.), Micropaleontology, special<br />
Publication vol. 6. Micropaleontology Press, American<br />
Museum of Natural History, New York. pp. 9-16.<br />
As the only planktic group commonly recovered from deposits<br />
of all Phanerozoic systems, <strong>radiolaria</strong>ns have special significance in<br />
discriminating deep basinal or oceanic marine environments of<br />
deposition through time. Assuming <strong>radiolaria</strong>n planktic habit has<br />
changed little since the Ordovician, they can be used for<br />
comparative environmental analysis for much of the Phanerozoic.<br />
This approach must be tempered by the realization that there is<br />
probably much yet to learn about the details of environmental<br />
response of pre-Mesozoic <strong>radiolaria</strong>ns. Radiolaria were clearly not<br />
the dominant planktic group throughout the Phanerozoic. However,<br />
their consistent association with other planktic organisms in the<br />
stratigraphic record and their association with facies inferred to be<br />
deeper-water validates their cautious use as indicators of distal<br />
basinal or oceanic environments from the Ordovician to the present.<br />
As such environments are often optimal sites for the preservation of<br />
abundant lipid-rich, organic material largely derived from<br />
phytoplankton, <strong>radiolaria</strong>ns are commonly associated with riche<br />
marine hydrocarbon source rocks irrespective of their age within the<br />
Phanerozoic. Other equally rich source rocks that are of nonmarine<br />
origin do not, of course, contain <strong>radiolaria</strong>ns. In addition to being<br />
associated with environmental settings favorable to the accretion<br />
and preservation of organic-rich sediments, <strong>radiolaria</strong>ns themselves<br />
may have been significant contributors to the ultimately preserved<br />
petroleum precursors, because certain living <strong>radiolaria</strong>ns are known<br />
to contain high levels of lipid material. Thus, Radiolaria may have had<br />
both environmental and some measure of causative association with<br />
the accumulation of organic-rich rocks which have the potential to<br />
become source rocks for hydrocarbons through most of the<br />
Phanerozoic.
Bibliography - 1993 Radiolaria 14<br />
Osozawa, S. & Okamura, M. 1993. New <strong>radiolaria</strong>n<br />
ages from the Troodos ophiolite and their tectonic<br />
implications. Island Arc, 2/1, 1-6.<br />
Newly obtained <strong>radiolaria</strong>n biostratigraphic age combined with<br />
previous isotopic age of the Troodos ophiolite shows that the<br />
ophiolite becomes systematically younger from east to west:<br />
Turonian, early Campanian, and late Campanian. The youngest late<br />
Campanian part of the ophiolite is directly covered by the<br />
volcaniclastic sediment derived from an active island arc, whereas<br />
the older part is covered by pelagic radiolarite. These facts<br />
constitute evidence that the Troodos ophiolite was probably<br />
emplaced during the subduction of an active spreading ridge.<br />
Pessagno, E.A., Blome, C.D., Hull, D.M. & Six,<br />
W.M. 1993. Jurassic Radiolaria from the Josephine<br />
ophiolite and overlying strata, Smith River subterrane<br />
(Klamath Mountains), northwestern California and<br />
southwestern Oregon. Micropaleontology, 39/2, 93-166.<br />
This report deals with me <strong>radiolaria</strong>n assemblage occurring<br />
within the Josephine ophiolite and in overlying sedimentary strata in<br />
the Western Klamath terrane, Smith River subterrane, northwestern<br />
California. Twenty-seven new species, eight new genera, and one new<br />
family (Bernoulliidae, n. fam.) are described from this succession. An<br />
emended definition is given for Parvicingula Pessagno and a new<br />
name is given for Andromeda Baumgartner. In addition, a revised<br />
<strong>radiolaria</strong>n zonation is presented for the Middle and Upper Jurassic.<br />
This new zonal scheme can be linked to both zonal schemes in Japan<br />
and Europe via first or last occurrence biohorizons of diagnostic<br />
taxa. Radiolarian biostratigraphic data from the Smith River and<br />
Rogue Valley subterranes is related to co-occurring megafossil<br />
chronostratigraphic data and to U/Pb geochronometry. Range,<br />
occurrence, and relative abundance of the more important taxa are<br />
shown in the text-figures. This investigation also establishes that<br />
well-preserved Radiolaria can be extracted from strata exposed to<br />
prehnite-pumpellyite facies metamorphism. Moreover,<br />
paleobiogeographic data are presented to substantiate tectonic<br />
transport of the Western Klamath terrane from low latitudes to high<br />
latitudes during the course of the Middle and Late Jurassic<br />
(Oxfordian-Callovian).<br />
Popova, I.M. 1993. Significance and paleoecological<br />
interpretations of early-middle Miocene <strong>radiolaria</strong>ns from<br />
south Sakhalin, Russia. In: Radiolaria of giant and subgiant<br />
fields in Asia. Nazarov Memorial Volume. (Blueford, J.R. &<br />
Murchey, B.L., Eds.), Micropaleontology, special<br />
Publication vol. 6. Micropaleontology Press, American<br />
Museum of Natural History, New York. pp. 161-174.<br />
Radiolarians from the deposits of five south Sakhalins sections<br />
were studied. Taxa found indicated a late early Miocene to early<br />
middle Miocene age of the Maruyamskaya, Kurashiidkaya, and<br />
Sertunaiskaya suites. The comparison of the South Sakhalin<br />
<strong>radiolaria</strong>n assemblages with the same age assemblages from the<br />
Deep Sea Drilling Project Holes 436 (Leg 58) and 438B (Leg 57)<br />
show a large taxonomic similarity especially from the Larcopyle<br />
polyacantha, Sphaeropyle rohusta and Eucyrtidium inflatum zones.<br />
Facies changes and <strong>radiolaria</strong>n assemblages in sections from the<br />
Krilyon Peninsula and the central part of Sakhalin Island show that<br />
early middle Miocene represents a phase of peak paleobasin<br />
transgression. Comparing <strong>radiolaria</strong>ns from similar age deposits<br />
from the Kuril, Japanese and Sakhalin Islands suggest a global<br />
oceanic level rise. The comparison of this data with the available<br />
scale of sea level fluctuations of the eastern Pacific near North<br />
America indicates possible synchronisms of middle Miocene<br />
transgressive phases in the northwest and northeast Pacific<br />
sectors.<br />
Saito, M. 1993. Geological significance of the "Toishitype"<br />
shale in the evolution of the Jurassic melanges in the<br />
Kuze area, western Mino Terrane, central Japan. Bull. geol.<br />
Surv. Japan, 44/9, 571-596. (in Japanese)<br />
Saito, M., Sugiyama, K. & Sato, Y. 1993.<br />
Cretaceous <strong>radiolaria</strong>ns from the Shimanto Supergroup in<br />
eastern Kagoshima Prefecture, and their geological<br />
significance. J. geol. Soc. Japan, 99/12, 1037-1040. (in<br />
Japanese)<br />
Saito, M., Teraoka, Y., Miyazaki, K. &<br />
Toshimitsu, S. 1993. Radiolarian fossils from the<br />
Nishikawauchi formation in the Onogawa Basin east Kyushu,<br />
and their geological significance. J. geol. Soc. Japan, 99/6,<br />
479-482. (in Japanese)<br />
- 102 -<br />
Saito, M. & Tsukamoto, H. 1993. Chert breccia, its<br />
occurrence and <strong>radiolaria</strong>n fossils in the Hichiso-Mugi area,<br />
central Mino Terrane, central Japan. J. geol. Soc. Japan,<br />
99/2, 117-133. (in Japanese)<br />
A detailed geological survey has revealed that the chert breccia<br />
conformably covers the Jurassic sandstone in the Hichiso-Mugi area.<br />
It shows that the chert-clastic sequence in the Kamiaso Unit<br />
consists of Early Triassic banded claystone, Middle Triassic to early<br />
Middle Jurassic chert, Middle Jurassic siliceous shale and shale, late<br />
Middle to Late (?) Jurassic turbidite and sandstone, and chert<br />
breccia in the ascending order. On the basis of field and laboratory<br />
evidence and the knowledge of the currently active subduction<br />
zones, the sedimentary process of chert and chert-limestone<br />
breccia formation is discussed. Clasts of the breccias came from<br />
the uppermost part of accretionaly complex and were supplied to the<br />
trench by submarine current in a submarine canyon or gravitational<br />
sliding on it.<br />
Sakakibara, M., Hori, R.S. & Murakami, T. 1993.<br />
Evidence from <strong>radiolaria</strong>n chert xenoliths for post-Early<br />
Jurassic volcanism of the Mikabu greenrocks, Okuki area,<br />
western Shikoku, Japan. J. geol. Soc. Japan, 99/10, 831-<br />
833. (in Japanese)<br />
Sakakibara, M., Isozaki, Y., Nanayama, F. &<br />
Narui, E. 1993. Radiolarian age of greenrock-chertlimestone<br />
sequence and its accretionary prodess of the Nikoro<br />
Group in the Tokoro belt, eastern Hokkaido, Japan. J. geol.<br />
Soc. Japan, 99, 615-627. (in Japanese)<br />
Sarnthein, M. & Faugères, J.C. 1993. Radiolarian<br />
contourites record Eocene AABW circulation in the equatorial<br />
East Atlantic. In: Contourites and bottom currents. (Stow,<br />
D.A.V. & Faugeres, J.C., Eds.), vol. 82/1-4. Sedimentary<br />
Geology, pp. 145-155.<br />
50 m of Middle Eocene pure <strong>radiolaria</strong>n ooze were drilled at ODP<br />
Site 660 in the equatorial East Atlantic, 80 km northeast of the<br />
Kane Gap. The oozes comprise a 10 m high and 2 km broad mound of<br />
seismic reverberations, covered by manganese-rich sediment, and<br />
contain trace amounts of sponge spicules and diatoms, negligible<br />
organic carbon (0.15%), clay, and variable amounts of pyrite. The<br />
yellow to pale brown silty sediments are relatively coarse-grained<br />
(30-45% coarser than 6 µm), little bioturbated, and commonly<br />
massive or laminated on a cm-scale. The unlithified <strong>radiolaria</strong>n ooze<br />
may indicate an interval of high oceanic productivity, probably linked<br />
to a palaeoposition of Site 660 close to the equatorial upwelling belt<br />
during Middle Eocene time. The absence of organic matter, however,<br />
and both the laminated bedding and the mound-like structure of the<br />
deposit on the lower slope of a continental rise indicate deposition<br />
by relatively intense contour currents of oxygen-rich deep water,<br />
which passed through the Kane Gap, winnowed the fine clay fraction,<br />
and prevented the preservation of organic carbon. The ooze may be<br />
either a contourite-lag deposit, or a contourite accumulation of<br />
displaced <strong>radiolaria</strong>ns, originating south of the Kane Gap and being<br />
deposited in its northern lee, thus documenting the passage of a<br />
strong cross-equatorial bottom-water current formed near<br />
Antarctica. These Eocene contourites may be an analogue for<br />
ancient radiolarites in the Tethyan Ocean.<br />
Sashida, K., Igo, H., Adachi, S., Koike, T.,<br />
Hisad, K.I. & Nakornsri, N. 1993. Occurrences of<br />
Paleozoic and Mesozoic <strong>radiolaria</strong>ns from Thailand and<br />
Malaysia and its geologic significance (preliminary report).<br />
N. Osaka Micropaleont. spec. Vol., 9, 1-17. (in Japanese)<br />
Sashida, K., Igo, H., Hisada, K.I., Nakornsri, N.<br />
& Amponmaha, A. 1993. Occurrence of Paleozoic and<br />
early Mesozoic Radiolaria in Thailand (preliminary report). J.<br />
Southeast Asian Earth Sc., 8/1-4, 97-108.<br />
Paleozoic and Early Mesozoic <strong>radiolaria</strong>ns are newly recovered<br />
from chert and associated fine-grained clastic rocks in Thailand.<br />
This study clarifies the geologic age of these <strong>radiolaria</strong>n rocks ant<br />
their paleogeographical and geotectonic significance. Devonian,<br />
Early Carboniferous ant Permian <strong>radiolaria</strong>ns were found in the "Fang<br />
Chert" which outcrops along the Chiang Mai-Fang Road, upper north<br />
Thailand. Early Carboniferous <strong>radiolaria</strong>ns were recovered from a<br />
sequence of tuffaceous shale ant chert exposed in the Pak Chom<br />
area along the Mekong River, and well-preserved Late Devonian ant<br />
Early Carboniferous <strong>radiolaria</strong>ns were also recovered from cherts<br />
exposed along the Pak Chom-Loei Road near Phu Laem, north of Loei,<br />
in northeast Thailant. These Devonian to Carboniferous <strong>radiolaria</strong>n<br />
faunas are apparently identical with those reported from eastern and<br />
western Australia. Well-preserved Early Triassic conodonts and
Radiolaria 14 Bibliography - 1993<br />
<strong>radiolaria</strong>ns were obtained from a limestone exposed near<br />
Patthalung, southern Thailand. Most of the <strong>radiolaria</strong>n species of this<br />
fauna show close affinity with those reported from the Upper<br />
Paleozoic rocks, and are new species except for some spicule-type<br />
forms. Based on the above-mentioned newly obtained<br />
micropaleontological evidence, the geotectonic significance of these<br />
<strong>radiolaria</strong>n rocks are briefly discussed in relation to the<br />
paleogeography of the Palaeo-Tethys Ocean, Sibumas and Indochina<br />
Terranes, and Australia during the Late Devonian to Middle Permian<br />
times.<br />
Sashida, K., Nishimura, H., Igo, H., Kazama, S.<br />
& Kamata, Y. 1993. Triassic <strong>radiolaria</strong>n faunas from Kisofukushima,<br />
Kiso Mountains, central Japan. Sci. Rep. Inst.<br />
Geosci., Univ. Tsukuba, Sect. B: geol. Sci., 14, 77-97.<br />
Moderately well-preserved Triassic <strong>radiolaria</strong>ns were recovered<br />
from a chert section along a valley north of Kisofukushima, Kiso<br />
Mountains, central Japan. Five Triassic <strong>radiolaria</strong>n assemblages are<br />
recognized in this section; three of Middle Triassic and two of Late<br />
Triassic in age. Middle Triassic assemblages are:<br />
Pseudostylosphaera japonica (middle Anisian), Pseudostylosphaera<br />
helicata (late Anisian-early Ladinian), Cryptostephanidium sp. (late<br />
Ladinian) Assemblages. Late Triassic assemblages are:<br />
Capnuchosphaera sp. (Carnian) and Betraccium sp. (early Norian)<br />
Assemblages. The age of these assemblages is directly controlled by<br />
co-occurring conodonts. We correlated these assemblages with<br />
those of local and foreign studies. Several selected <strong>radiolaria</strong>n<br />
species are illustrated and systematically described in this paper.<br />
Sharma, V. & Singh, S. 1993. Radiolarian<br />
biostratigraphy of early Pliocene sequences, Car Nicobar<br />
Island, northeast Indian Ocean. J. geol. Soc. India, 41/3,<br />
199-213.<br />
A study of the <strong>radiolaria</strong>n assemblage from the Sawai Bay<br />
Formation (Early Pliocene) exposed in Car Nicobar Island shows the<br />
presence of age diagnostic <strong>radiolaria</strong>n taxa. Based on the <strong>radiolaria</strong>n<br />
zonation applicable for the tropical Indian Ocean, three <strong>radiolaria</strong>n<br />
zones are identified in this formation. These, in ascending order, are:<br />
Phormostichoartus dolfolum zone, P. fistula zone and Stichocorys<br />
peregrina Zone. The <strong>radiolaria</strong>n events (first and last appearances)<br />
recognised in the Car Nicobar sequences are discussed in relation to<br />
those in the Central Indian Ocean Basin. The proposed <strong>radiolaria</strong>n<br />
zones are correlated with the previously proposed planktonic<br />
foraminiferal zone in the study area, and an integrated<br />
biostratigraphic scheme is presented.<br />
Sharma, V., Srinivasan, M.S. & Mahapatra, A.K.<br />
1993. Early Miocene <strong>radiolaria</strong>n and planktonic foraminiferal<br />
biostratigraphy, North Passage Island, Andaman Sea. J. geol.<br />
Soc. India, 42/2, 154-162.<br />
The Early Miocene sequences of North Passage Island in the<br />
Andaman Sea have been studied for their siliceous and calcareous<br />
microfossil assemblages. 95 species of <strong>radiolaria</strong> and 27 species of<br />
planktonic foraminifera belonging to these two major groups of<br />
microfossils have been documented. An integrated <strong>radiolaria</strong>n and<br />
planktonic foraminiferal biostratigraphy is presented.<br />
Spencer-Cervato, C., Lazarus, D.B., Beckman,<br />
J.P., Von Salis Perch-Nielsen, K. & Biolzi, M.<br />
1993. New calibration of Neogene <strong>radiolaria</strong>n events in the<br />
North Pacific. In: Interrad VI. (Lazarus, D.B. & De Wever, P.,<br />
Eds.), vol. 21/4. Special Issue: Marine Micropal., Elsevier,<br />
Amsterdam. pp. 261-293.<br />
New age models for twelve Deep Sea Drilling Project sites in the<br />
North Pacific have been produced, based on (in order of importance<br />
in our dataset) a recompilation of previously published diatom,<br />
calcareous nannofossil and foraminifer first and last occurrences,<br />
and magnetostratigraphy. The projected ages of <strong>radiolaria</strong>n first and<br />
last occurrences derived from the line of correlation of the<br />
age/depth plots have been computed from these sites, and 28<br />
<strong>radiolaria</strong>n events have thereby been newly cross calibrated to North<br />
Pacific diatom and other stratigraphy. Several of the North Pacific<br />
<strong>radiolaria</strong>n events are older than in previously published equatorial<br />
Pacific calibrations, and some may be diachronous within the North<br />
Pacific. These patterns may be due to complex latitudinal patterns of<br />
clinal variation in morphotypes within lineages, or to migration<br />
events from the North Pacific towards the Equator.<br />
Stamatakis, M.G. & Hein, J.R. 1993. Origin of barite<br />
in Tertiary marine sedimentary rocks from Lefkas Island,<br />
Greece. Econ. Geol., 88/1, 91-103.<br />
- 103 -<br />
Siliceous and calcareous biogenic rocks host pervasive,<br />
although volumetrically minor, authigenic barite on Lefkas Island,<br />
Greece. The barite composes up to 10 percent of the carbonate-free<br />
fraction of samples. In decreasing order of abundance, authigenic<br />
barite occurs as infilled foraminifera and <strong>radiolaria</strong>n tests,<br />
disseminated grains and aggregates in porcelanite and siliceous<br />
limestone, replaced siliceous and calcareous biogenic tests, and thin<br />
laminae and lenses. The laminae form anastomosing networks that<br />
were probably originally rich in organic matter. Barite abundance<br />
shows a good correlation with the abundance of skeletal biogenic<br />
components. Biogenic silica diagenesis produced opal-CT and<br />
clinoptilolite, which compose the cement of porcelanite, replaced<br />
<strong>radiolaria</strong>ns, diatoms, and echinoderms and filled in some<br />
foraminifera tests. Subsequent silica diagenesis produced<br />
chalcedony at deeper stratigraphic levels, which also filled in pore<br />
space and calcareous microfossils in siliceous limestones and<br />
formed chert beds. Textural evidence shows that barite<br />
mineralization postdated opal-CT formation and preceded<br />
chalcedony formation Barite precipitated in microenvironments<br />
including microfossil chambers, fecal pellets, and areas rich in<br />
organic matter. The source of the barium was probably from the<br />
decomposition of organic matter derived from plankton and bacteria<br />
and from the diagenesis of silica and carbonate tests. The source of<br />
the sulfate ion was seawater; possibly additional sulfate was<br />
produced and utilized in microenvironments from degradation of<br />
organic matter.<br />
Sugie, H. 1993. Analysis of paleoenvironment by<br />
<strong>radiolaria</strong>ns in the late Miocene Arakawa Group (Tochigi<br />
Prefecture, Japan). N. Osaka Micropaleont. spec. Vol., 9,<br />
313-335. (in Japanese)<br />
Sugiyama, K. 1993. Skeletal structures of lower and middle<br />
Miocene Lophophaenids (Radiolaria) from central Japan.<br />
Trans. Proc. palaeont. Soc. Japan, n. Ser., 169, 44-72.<br />
Nine species of five lophophaenid genera are described from<br />
the Lower Miocene Toyohama Formation, Morozaki Group, Aichi<br />
Prefecture and the lowest Middle Miocene Oidawara Formation,<br />
Mizunami Group, Gifu Prefecture, central Japan. A special attention<br />
is given to describing and illustrating the details of their skeletal<br />
structures which possess one or two horizontal rings, since it is<br />
believed that these details are important in establishing the<br />
taxonomy and clarifying the phylogenetic relationships. The<br />
examination discriminates seven types of skeletal structure. Four<br />
species are newly described, and two new genera, Steganocubus and<br />
Cryptogyrus, are also erected herein.<br />
Sugiyama, K., Ozawa, T., Kuroyanagi, Y. &<br />
Furutani, H. 1993. Stratigraphy and <strong>radiolaria</strong>n fossils of<br />
the Jurassic Shiranezaki formation (new name) and the<br />
Cretaceous Matsuo Group in the eastern part of Shima<br />
Peninsula, Mie Prefecture, central Japan. N. Osaka<br />
Micropaleont. spec. Vol., 9, 191-203. (in Japanese)<br />
Suzuki, H. 1993. The Canoptum assemblage (Radiolaria)<br />
from the Umenoki unit (the northern Chichibu Belt) in the<br />
Kamikatsu Town area. N. Osaka Micropaleont. spec. Vol., 9,<br />
109-117. (in Japanese)<br />
Takahashi, K. & Ling, H. 1993. Cretaceous<br />
<strong>radiolaria</strong>ns from the Ontong Java Plateau, Western Pacific,<br />
holes 803D and 807C. In: Proceedings of the Ocean Drilling<br />
Program, Scientific Results. (Berger, W.H., L.W., K., Mayer,<br />
L.A. et al., Eds.), vol. 130. College Station, TX (Ocean<br />
Drilling Program), pp. 93-102.<br />
Among the five sites drilled during Ocean Drilling Program Leg<br />
130, two deep holes (803D and 807C) penetrated Cretaceous<br />
sediments overlying the basaltic pillows, flows, and possibly<br />
basement rocks. Abundant, poorly preserved <strong>radiolaria</strong>ns with<br />
limited diversity were recovered from a few horizons within the<br />
sediments proximal to the basalt. At Site 803, three thin layers of<br />
radiolarites interbedded with claystone and clayey siltstone yielded<br />
<strong>radiolaria</strong>n assemblages of late Albian age. At Site 807, several<br />
layers of <strong>radiolaria</strong>n siltstones were recovered proximal to the<br />
basalt. Among them the most significant <strong>radiolaria</strong>n assemblage is<br />
an Aptian fauna, located approximately 7 m above the basaltic flows.<br />
The Aptian <strong>radiolaria</strong>n age for Site 807 is at least in accord with<br />
those suggested by planktonic foraminifer and paleomagnetic<br />
evidence. These Cretaceous <strong>radiolaria</strong>ns are the oldest assemblages<br />
recorded from the Ontong Java Plateau region.<br />
Takahashi, O. & Ishii, A. 1993a. Oligocene<br />
<strong>radiolaria</strong>ns from the southern margin of the Kobotoke
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Group, Kanto Mountains, central Japan. J. geol. Soc. Japan,<br />
99/4, 289-291. (in Japanese)<br />
Takahashi, O. & Ishii, A. 1993b. Paleo-oceanic<br />
environment in the latest Cretaceous time, inffered from<br />
<strong>radiolaria</strong>n fauna of Amphipyndax tylotus Zone. N. Osaka<br />
Micropaleont. spec. Vol., 9, 261-270. (in Japanese)<br />
Takami, M., Isozaki, Y., Nishimura, Y. & Itaya,<br />
T. 1993. Effect of detrital white mica and contact<br />
metamorphism to K-Ar dating of weakly metamorphosed<br />
accretionary complex - an example of Jurassic accretionary<br />
complex in eastern Yamaguchi Prefecture, southwest Japan. J.<br />
geol. Soc. Japan, 99/7, 545-563. (in Japanese)<br />
Takashiroyama-Research-Group 1993. A new<br />
information on the geological history of the Tamba Belt,<br />
southwest Japan. Earth Sci., J. Assoc. geol. Collab. Japan,<br />
47/6, 549-554. (in Japanese)<br />
Takemura, A. & Yamakita, S. 1993. Late Permian<br />
Neoalbaillella assemblage (Radiolaria) from a phospate<br />
nodule in the Chichibu Belt, Shikoku, Japan. N. Osaka<br />
Micropaleont. spec. Vol., 9, 41-49.<br />
Takemura, S., Suzuki, S. & Ishiga, H. 1993.<br />
Stratigraphy of the Kozuki formation, "Kamigori Zone",<br />
southwest Hyogo Prefecture, Japan, reconsideration with the<br />
discovery of Albaillella asymmetrica (<strong>radiolaria</strong>n fossil) and<br />
the structural analysis. J. geol. Soc. Japan, 99, 675-678. (in<br />
Japanese)<br />
Taketani, Y. 1993. Radiolarian fossils from the Site of<br />
Ikego Ammunition Depot, Zushi City, Kanagawa Prefecture.<br />
Final Report of Research on Fossil Calyptogena in Ikego,<br />
Yokohama Defence Facilities Administration Bureau, , 341-<br />
344. (in Japanese)<br />
Theodhori, P., Peza, L.H. & Pirdeni, A. 1993.<br />
Cretaceous pelagic and flysch facies of the Krasta-Cukali<br />
Zone, Albania. Cretaceous Res., 14/2, 199-209.<br />
The upper Tithonian to Upper Cretaceous and lower Tertiary<br />
pelagic and flysch facies of the Krasta-Cukali zone in central<br />
Albania are described from several stratigraphic sections, five in the<br />
northern Cukali subzone and three in the larger central and southern<br />
Krasta subzone. Preliminary facies analysis shows that pelagic<br />
deposition in the Cukali subzone was at a greater depth than that of<br />
the Krasta subzone, and that no terrigenous clastics reached this<br />
basin. Ophiolitic detritus derived from the eastern Mirdita zone is<br />
found in the Krasta subzone. Radiolaria and planktonic foraminifers<br />
allow a generalized biostratigraphic correlation between the<br />
sections. The palaeogeographic evolution of the zone is also<br />
outlined.<br />
Ueda, H., Kawamura, M. & Iwata, K. 1993.<br />
Occurrence of the Paleocene <strong>radiolaria</strong>n fossils from the<br />
Idon'nappu Belt, central part of Hokkaido, Northern Japan. J.<br />
geol. Soc. Japan, 99/7, 565-568. (in Japanese)<br />
Vishnevskaya, V. 1993. Jurassic and Cretaceous<br />
<strong>radiolaria</strong>n biostratigraphy in Russia. In: Radiolaria of giant<br />
and subgiant fields in Asia. Nazarov Memorial Volume.<br />
(Blueford, J.R. & Murchey, B.L., Eds.), Micropaleontology,<br />
special Publication vol. 6. Micropaleontology Press,<br />
American Museum of Natural History, New York. pp. 175-<br />
200.<br />
Jurassic and Cretaceous <strong>radiolaria</strong>n faunas from carbonate and<br />
siliceous rock sequences of the Greater and Lesser Caucasus and<br />
volcaniclastic and siliceous rock sections from the Koryak upland,<br />
Kamchatka, Sakhalin and Sichote-Alin were investigated. As a result<br />
of this biostratigraphical research, thirteen Tethyan <strong>radiolaria</strong>n<br />
assemblages and eleven Pacific Rim assemblages were<br />
distinguished. The ages of the Tethyan <strong>radiolaria</strong>n associations were<br />
calibrated with ammonites, inoceramids and planktonic foraminifers.<br />
These <strong>radiolaria</strong>n assemblages can be considered as zonal for the<br />
southern part of Eurasia. The <strong>radiolaria</strong>n zonal scheme for the<br />
volcanogenic-siliceous sequences from the far eastern part of<br />
Russia (Pacific Rim) is less detailed because the rocks contain few<br />
other microfauna or macrofossils. However, even in these rocks,<br />
radiolanan assemblages can be used for division and correlation of<br />
- 104 -<br />
sections in order to study the Mesozoic stratigraphy of Pacific<br />
folded belts. Radiolarians are particularly useful for reconstructions<br />
of tectonically complex fragmentary sections. The discovery of wellpreserved,<br />
abundant Jurassic and Cretaceous <strong>radiolaria</strong>ns in Russia<br />
contributes to a reliable <strong>radiolaria</strong>n biostratigraphy and increases<br />
the opportunity to use these microfossils for global correlation.<br />
Vishnevskaya, V.S., Merts, A.V. & Sedaeva,<br />
K.M. 1993. Devonian <strong>radiolaria</strong>ns as possible generators of<br />
oil. Dokl. Akad. Nauk SSSR, 333/6, 745-749.<br />
Wang, R.J. 1993. Fossil Radiolaria from Kufeng formation<br />
of Chaohu, Anhui. Acta palaeont. sinica, 32/4, 442-457.<br />
Recently, diverse, abundant and well-preserved <strong>radiolaria</strong>ns<br />
have been discovered from the chert of the Kufeng Formation<br />
(Permian) in Chaohu, Anhui, among which fourteen genera, thirty-six<br />
species (including two new species, Latentifistula triradiata and<br />
Quadriremis flata), and one unnamed spheroidal form are recognized<br />
and described. These <strong>radiolaria</strong>ns are composed of three basic type<br />
microfossils, namely, the albaillellids, the spherical polycystine and<br />
the stauraxon polycystine, with such dominant elements as<br />
Pseudoalbaillella scalprata, P. longtanensis, P. sp. cf. P. Iongicornis,<br />
Phaenicosphaera mammilla, P. sp. A, Ruzhencevispongus uralicus, R.<br />
sp. A and R . sp. B. Based on the distribution pattern of the<br />
<strong>radiolaria</strong>ns in the Kufeng Formation, two assemblage zones have<br />
been proposed, namely the Pseudoalbaillella scalprata-P. sp. cf. P.<br />
Iongicornis Assemblage in the lower part and the Phaenicosphaera<br />
mammilla-Ruzhencevispongus uralicus Assemblage in the upper part.<br />
Biostratigraphically, the first assemblage is correlated with the<br />
Pseudoalbaillella scalprata-P. fusiformis Assemblage from the<br />
Kufeng Formation at Longtan, Nanjing and the Pseudoalbaillella sp. C<br />
Assemblage of Southwest Japan, while the second assemblage is<br />
considered as equivalent to the Phaenicosphaera mammilla<br />
Assemblage from the Kufeng Formation at longtan, Nanjing and<br />
Hegleria mammifera (= Phaenicosphaera mammilla Sheng et Wang )<br />
from West Texas, USA and correlated with the Ruzhencevispongus<br />
uralicus Assemblage of the Southern Urals, USSR. Therefore, it is<br />
considered that the two zones fall into early Maokouan and middle to<br />
late Maokouan stage respectively, and correspond to early and<br />
middle to late Guadalupian.<br />
Wang, Y.J. 1993. Middle Ordovician <strong>radiolaria</strong>ns from the<br />
Pingliang Formation of Gansu Province, China. In:<br />
Radiolaria of giant and subgiant fields in Asia. Nazarov<br />
Memorial Volume. (Blueford, J.R. & Murchey, B.L., Eds.),<br />
Micropaleontology, special Publication vol. 6 .<br />
Micropaleontology Press, American Museum of Natural<br />
History, New York. pp. 98-114.<br />
Middle Ordovician <strong>radiolaria</strong>ns were collected from the sandy<br />
limestone of the lower member of the Pinglinng Formation of Gansu<br />
province, China. The <strong>radiolaria</strong>n fauna contains five genera and more<br />
than ten species belonging to the spherical polycystines of the<br />
family Inaniguttidae. These genera include Inanihella, Inanigutta,<br />
Oriundogutta, Cessipylorum and Inanihigutta. Seven of these species<br />
(Inanihella penrosei, Inanigutta complanta, Oriundogutta cornuta, O.<br />
nazarovi, O. miscella miscella, Cessipylorum sp. cf. C. aperta and<br />
Inanihigutta verrucula) are identical with those of the Middle<br />
Ordovician Llandeilian-lower Caradocian of eastern Kazaichstan,<br />
(Nazarov 1975; Nazarov and Popov 1980). The graptolite<br />
Nemagraptus gracilis Zone (Syndyograptus subzone) and conodont<br />
Pygodus anserrinus Zone associated with the <strong>radiolaria</strong>n fauna are in<br />
accordance with Llandeilian-lower Caradocian in age.<br />
Welling, L.A. & Pisias, N.G. 1993. Seasonal trends<br />
and preservation biases of polycystine <strong>radiolaria</strong> in the<br />
northern California current system. Paleoceanography, 8/3,<br />
351-372.<br />
We analyzed a 2-year sediment trap record of 76 species of<br />
Radiolaria from three locations across the northern California<br />
Current System. Q-mode factor analysis identifies the fundamental<br />
trends in the <strong>radiolaria</strong>n data with a five-factor model that explains<br />
86% of the trap data. The factor assemblages that emerge from this<br />
analysis have temporal and spatial aspects that reflect fundamental<br />
oceanographic features of the eastern North Pacific. The most<br />
dominant process revealed by this analysis is related to the<br />
seasonality of the Califomia Current. Two factors illustrate this: the<br />
California Current factor, which has highest loadings during summer<br />
and fall, and the Winter factor, which is most important in the winter<br />
and spring. Together they account for 75% of the information in the<br />
trap samples from the two moorings located in the coastal region<br />
extending to ~300 km offshore. The oceanic environment sampled<br />
by the mooring 650 km offshore is strongly influenced by<br />
transitional waters and those from the Central and Subarctic Gyres.<br />
Loadings of the three factors related to these oceanographic regions<br />
show marked differences between years, which illustrates the
Radiolaria 14 Bibliography - 1993<br />
latitudinal variability in the divergence of the North Pacific Current.<br />
Spatial distributions of the trap factors in surface sediments<br />
beneath the California Current System generally agree with the<br />
temporal and spatial patterns they exhibit in the traps. Nonetheless,<br />
the trap factor model can only describe up to 50% of the <strong>radiolaria</strong>n<br />
sediment data, which means the species ratios in the sediment traps<br />
are significantly different than those in the sediments. A factor<br />
model using only robust specie's reveals the same basic trends as<br />
the first analysis, but the culled model is able to describe a larger<br />
fraction of the sediment data (63%-91% in sediments directly<br />
beneath the mooring sites). However, the increase in the amount of<br />
sediment data explained by the culled model is not distributed<br />
equally across all factors but is due to very high estimates of one<br />
factor in the coastal sediments, the California Current factor. At the<br />
Nearshore mooring site (130 km I offshore) this factor explains<br />
69% of the sediment data versus only 32% of the data in the traps<br />
where it was derived. This discrepancy suggests that either these<br />
two years of trap data are anomalous and have underestimated the<br />
predominance of the California Current assemblage over long time<br />
periods or the culled factor model, rather than eliminating the<br />
dissolution bias, actually overemphasizes the importance of wellpreserved<br />
species in the coastal environment.<br />
Widz, D. & De Wever, P. 1993. Nouveaux Nassellaires<br />
(Radiolaria) des radiolarites jurassiques de la coupe de<br />
Szeligowy Potok (Zones de Klippes de Pieniny, Carpathes<br />
Occidentales, Pologne). Rev. Micropaléont., 36/1, 77-91.<br />
One new genus and 6 new species of Nassellaria (Birkenmajeria<br />
n. gen., Gongylothorax szeligowiensis n. sp., Obesacapsula nodosa n.<br />
sp., Parahsuum carpathicum n. sp., Saitoum dercourti n. sp.,<br />
Spongocapsula dumitricai n. sp., Williriedellum sujkowskii n. sp.) are<br />
described from Oxfordian-Kimmeridgian (UA 7-8, UA 8, UA 9)<br />
radiolarites of the Szeligowy Potok section (Grajcarek Unit, Pieniny<br />
Klippen Belt). Some taxonomic remarks are given for several species<br />
of Nassellaria.<br />
Wu, H. 1993. Upper Jurassic and Lower Cretaceous<br />
<strong>radiolaria</strong>ns of Xialu chert, Yarlung Zangbo ophiolite belt,<br />
southern Tibet. In: Radiolaria of giant and subgiant fields in<br />
Asia. Nazarov Memorial Volume. (Blueford, J.R. & Murchey,<br />
B.L., Eds.), Micropaleontology, special Publication vol. 6.<br />
Micropaleontology Press, American Museum of Natural<br />
History, New York. pp. 115-136.<br />
Well preserved <strong>radiolaria</strong>n fossils were found in the Xialu ribbon<br />
chert on the southern side of Yarlung Sangbo ophiolite in southern<br />
Tibet. Based on the correlation with the <strong>radiolaria</strong>n zonations of<br />
western North America and other areas, the age of the Xialu chert<br />
can be assigned to Upper Jurassic (upper Kimmeridgian-lower<br />
Tithonian) - Lower Cretaceous (upper Valanginian). This provides<br />
important evidence for reconstructing geological history of east<br />
Tethys and shows <strong>radiolaria</strong>ns to be very important stratigraphic<br />
tools in long distance correlation even between different<br />
paleogeographic realms. Two new genera and nineteen new species<br />
are described.<br />
Yamagata, T. 1993. Occurrence of Jurassic <strong>radiolaria</strong>ns<br />
from mudstone of the Ryozensan formation, Suzuka<br />
Mountains, central Japan. N. Osaka Micropaleont. spec.<br />
Vol., 9, 143-149. (in Japanese)<br />
Yamamoto, K. 1993. Analysis of sediemntary depth based<br />
on quantitative analysis for <strong>radiolaria</strong>n assemblages. N.<br />
Osaka Micropaleont. spec. Vol., 9, 249-259. (in Japanese)<br />
Yamaoka, Y. 1993. Geological relationship between<br />
metamorphic rocks and non-metamorphic rocks in Jurassic<br />
Terrane and their time as an accretionary complex in<br />
northwestern part of Tsuyama City, Okayama Prefecture,<br />
southwest Japan. N. Osaka Micropaleont. spec. Vol., 9, 151-<br />
163. (in Japanese)<br />
Yamasaki, T., Yokota, Y. & Okumura, K. 1993.<br />
Cretaceous <strong>radiolaria</strong>ns from the eastern part of Aki City,<br />
Kochi Prefecture - with reference to the boundary between the<br />
north and south Shimanto Subbelts. N. Osaka Micropaleont.<br />
spec. Vol., 9, 215-223. (in Japanese)<br />
Yanase, A. & Isozaki, Y. 1993. Lithostratigraphy and<br />
<strong>radiolaria</strong>n age of Permian accretionary complex in Kiku<br />
Peninsula, northern Kyushu. J. geol. Soc. Japan, 99/4, 285-<br />
288. (in japanese)<br />
- 105 -<br />
Yang, Q. 1993. Taxonomic Studies of Upper Jurassic<br />
(Tithonian) Radiolaria from the Taman Formation, eastcentral<br />
Mexico. Paleoworld, 3, 1-164.<br />
The upper Tithonian Radiolaria (Upper Jurassic; Zone 4) of the<br />
Taman Formation represent a highly abundant and diversified fauna<br />
of outer neritic to bathyal environment. Thirteen families (one new),<br />
forty-four genera (seven new), and one hundred and seventy-two<br />
species level taxa (forty-nine new) are documented herein.<br />
Biostratigraphically important taxa present in this assemblage<br />
include Acanthocircus dicranocanthos, Vallupus hopsoni, Bivallupus,<br />
Parvicingula excelsa, and Perispyridium. The distinctive Jurassic<br />
"marker" Perispyridium rapidly decreases in abundance towards the<br />
top of Subzone 4 beta and does not occur in Subzone 4 alpha.<br />
Curiously, the Taman <strong>radiolaria</strong>n fauna is poor in Mirifusus and<br />
completely lacks Ristola altissima, R. procera, Eucyrtidiellum<br />
ptyctum, and Sethocapsa(?) cetia, which are common, distinctive<br />
upper Tithonian elements elsewhere. This <strong>radiolaria</strong>n fauna is<br />
associated with ammonites, calpionellids, and pectenacids. It<br />
includes the Kossmatia-Durangites assemblage and the lower part of<br />
Substeueroceras-Proniceras assemblage of Imlay (1980).<br />
Furthermore, the base of Zone 4 corresponds closely to the first<br />
occurrence of hyaline calpionellids. The <strong>radiolaria</strong>n assemblage is<br />
correlated with <strong>radiolaria</strong>n faunas in other areas, such as the Cape<br />
Verde Basin (East Atlantic) and Oman. Additionally, a new genus<br />
(Loopus, Family Pseudodictyomitridae), described herein from the<br />
Taman, bridges the correlation of Tithonian between North America<br />
and Japan.<br />
Subfamilies Tetraditryminae Baumgartner and Higumastrinae<br />
Baumgartner are treated herein as synonyms on the basis of their<br />
internal test structure. Two new genera (Neoparonaella and<br />
Pseudohigumastra) of the Family Hagiastridae and one new genus<br />
(Tetnastrum) of Spumellariina family incertae sedis are erected<br />
herein.<br />
The Acaeniotylidae, n. fam., is established herein to include a<br />
unique group of Radiolaria represented by the well-known genus<br />
Acaeniotyle Foreman. The new family is characterized by having a<br />
tubercular cortical shell, a latticed medullary shell and a number<br />
(varying among genera) of secondary spines on the test surface.<br />
Three new genera (Acastea, Acusten and Praeconosphaera) of this<br />
family are erected herein, and Genus Acaeniotyle Foreman is<br />
emended. The following families are common in the Taman (Zone 4):<br />
Acaeniotylidae, n. fam., Hagiastridae, Patulibracchiidae, Hsuidae,<br />
Parvivaccidae, Parasaturnalidae (Acanthocircus), Epitingiidae<br />
(Perispyridium), Archaeodictyomitridae, Pseudodictyomitridae,<br />
Syringocapsidae, Xiphostylidae, and Ultranaporidae (Napora).<br />
Paleobiogeographically, the upper Tithonian Taman faunas<br />
described herein belong to the Northern Tethyan Province of<br />
Pessagno et al. (1 987a), because of the common occurrence of<br />
both Pantanelliidae and Parvicingula and the lack of Ristola.<br />
Yang, Q., Mizutani, S. & Nagai, H. 1993.<br />
Biostratigraphic correlation between the Nadanhada Terrane<br />
of NE China and the Mino Terrane of central Japan. J. Earth<br />
Sci. Nagoya Univ., 40, 27-43.<br />
A biostratigraphic analysis of available data from the<br />
Nadanhada terrane, northeast China, and the Mino terrane, central<br />
Japan, shows that the Paleozoic limestone strata occurring in exotic<br />
blocks in both terranes contain similar fusulinid zones, ranging in<br />
age from Late Carboniferous Moscovian to Late Permian<br />
Changhsingian; but so far, no Permo-Carboniferous <strong>radiolaria</strong>n chert<br />
has been reported from the Nadanhada area. Triassic and lower<br />
Jurassic <strong>radiolaria</strong>n chert strata from both areas contain identical<br />
<strong>radiolaria</strong>n faunas. Lower Jurassic and Middle Jurassic fine clastic<br />
sediments of the two areas have similar <strong>radiolaria</strong>n and ammonite<br />
faunas, although there are a few differences in faunal composition.<br />
Late Jurassic and Early Cretaceous biostratigraphy of the two areas<br />
shows discernibly diverging features.<br />
Yao, A., Jie, Y. & An, T.X. 1993. Late Paleozoic<br />
<strong>radiolaria</strong>ns from the Guizhou and Guangxi areas, China. J.<br />
Geosci. Osaka City Univ., 36, 1-13.<br />
Late Paleozoic <strong>radiolaria</strong>ns were found from the Upper<br />
Paleozoic siliceous and clastic sediments on the Yangtze Platform in<br />
the Guizhou and Guangxi areas, South China. Three <strong>radiolaria</strong>n<br />
faunas were preliminarily distinguished, namely, the late<br />
Carboniferous to early Permian fauna, the late Middle Permian fauna<br />
and the Late Permian fauna. The first fauna, represented by<br />
Pseudoalbaillella uforma and P. cf. annulata, occurs in chert layers<br />
interbedded with limestone. The second, containing Follicucullus<br />
scholasticus and stauraxon polycystines, is from chert layers of the<br />
Gufeng Formation. The last fauna, characterized by Albaillella<br />
triangularis, A. excelsa, A. Ievis and Neoalbaillella optima, is from<br />
chert nodules within limestone of the Changxing Formation, from<br />
mudstone land chert of the Dalong Formation, and from their<br />
equivalents.
Bibliography - 1994 Radiolaria 14<br />
Aitchison, J.C. 1994. Early Cretaceous (Albian/Aptian)<br />
<strong>radiolaria</strong>ns from Blocks in Ayer Complex Melange, eastern<br />
Sabah, Malaysia with comments on their regional tectonic<br />
significance and the origins of enveloping melanges. J.<br />
Southeast Asian Earth Sc., (in press).<br />
Aitchison, J.C. & Flood, P.G. 1994. Cenozoic<br />
<strong>radiolaria</strong>ns from Ocean Drilling Program Leg 143, Site 869A<br />
Equatorial Pacific Ocean. In: Proceedings of the Ocean<br />
Drilling Program, Scientific Results. vol. 143. College<br />
Station, TX (Ocean Drilling Program). (in press)<br />
Amon, E.O. & Braun, A. 1994. Radiolarians from lower<br />
Permian deposits of the Belskaya depression, Bashkiria (west<br />
slope of southern Urals; Artinskian stage, Burtsevsky<br />
horizon). In: Contributions to Eurasian Geology; Permian<br />
Conference Papers. Eds.), vol. 9. Occasional Publications<br />
ESRI, Columbia, USA. pp. 1-7.<br />
From marly deposits of the Tulkas type section (Belskaya<br />
depression, Bashkiria) a well preserved Lower Permian (Artinskian)<br />
<strong>radiolaria</strong>n faunas is figured and described: Astroentactinia speciosa<br />
n. sp., Entactinia densissima, Entactinia aff. pycnoclada,<br />
Helioentactinia cf. ikka, Copicyntra leviuscula n. sp., Tetracircinata<br />
reconda Latentibifistula cf. triacanthophora, Quadriremis? sp.,<br />
Quinqueremis clathrolobulatus n. sp. Peculiarites of fauns<br />
compositio are briefly discussed.<br />
Bohrmann, G., Abelmann, A., Gersonde, R.,<br />
Hubberten, H. & Kuhn, G. 1994. Pure siliceous ooze, a<br />
diagenetic environment for early chert formation. Geology,<br />
22/3, 207-210.<br />
The formation of marine opal-CT nodules or layers as early<br />
diagenetic deposits has been documented only in Antarctic deep-sea<br />
sediments. In contrast, porcellanites and cherts in land sections and<br />
Deep Sea Drilling Project and Ocean Drilling Program drill sites are<br />
usually found in sediment sections of Miocene age and older. During<br />
R.V. Polarstern cruises ANT-IV3 and 4, young porcellanites were<br />
recovered for the first time in contact with their host sediment in<br />
two cores from the Atlantic sector of the southern ocean. Chemical<br />
and mineralogical studies of these deposits and their surrounding<br />
sediments have increased knowledge about very early chert<br />
formation. In both cores the porcellanites are embedded in<br />
sediments rich in opal-A with extremely low levels of detrital<br />
minerals, an environment that seems conducive to a rapid<br />
transformation of biogenic silica into porcellanites.<br />
Haslett, S.K. 1994a. Plio-Pleistocene <strong>radiolaria</strong><br />
biostratigraphy and palaeoceanography of the mid-latitude<br />
North Atlantic (DSDP Site 609). Geol. Mag., 131/1, 57-66.<br />
Radiolaria were examined throughout the Plio-Pleistocene of<br />
Deep Sea Drilling Project (DSDP) Site 609. Eight <strong>radiolaria</strong>n datumlevels<br />
(first and last appearances) were identified, some for the first<br />
time in the North Atlantic. The recognition of these datums allows<br />
correlation between the Atlantic, Pacific and Indian oceans, through<br />
a previously published zonal scheme (Johnson et al. 1989). Zones<br />
NR1 to NR11 were recognized, although some zones had to be<br />
combined (NR1-2 and NR8-10) due to the absence of some<br />
stratigraphically important taxa. The relative abundance distribution<br />
of the <strong>radiolaria</strong>n palaeoceanographical proxy Didymocyrtis<br />
tetrathalamus indicated three cool phases (0/0.56-0.75 Ma, 1.2-<br />
1.33/1.69-1.86 Ma, and 2.14 2.32/3.73-> 4.1 Ma) interrupted by<br />
two relatively warm episodes (0.56-0.75/1.2-1.33 Ma and 1.69-<br />
1.86/2.14-2.35 Ma). These fluctuations in sea-surface<br />
temperature (SST) correspond with palaeoclimatic events indicated<br />
by other proxies (e.g. Foraminifera), such as the onset of Northern<br />
Hemisphere glaciation. This study illustrates the usefulness of<br />
<strong>radiolaria</strong> in North Atlantic stratigraphical and palaeoceanographical<br />
analysls .<br />
Haslett, S.K. 1994b. Plio-Pleistocene <strong>radiolaria</strong>n<br />
biostratigraphy and palaeoceanography of the North<br />
Atlantic. In: Tectonic, Sedimentation and Palaeoceanography<br />
of the North Atlantic. (Scrutton, R.A. & Stoker, M.S., Eds.).<br />
Special Publications of the Geological Society of London,<br />
London, U.K. pp.<br />
Milliman, J.D. & Takahashi, K. 1994. Carbonate and<br />
opal production and accumulation in the ocean. In: Global<br />
1994<br />
- 106 -<br />
Surficial Geofluxex: Modern to Glacial. (Usselman, T.M.,<br />
Hay, W. & Meybeck, M., Eds.) . National Academy Press. (in<br />
press)<br />
Calcium carbonate and biogenically produced opal account for<br />
the deposition of nearly 1.8 x 10 14 t of sediment annually. Recent<br />
advances in documenting rates of production and sediment<br />
accumulation have facilitated a greater quantitative understanding<br />
of the carbonate and opal systems in the marine environment.<br />
Although reefs, atolls and carbonate banks occupy less than 1<br />
percent the area of the deep sea, they produce 25 to 250 times<br />
more carbonate per unit surface area than planktonic organisms. As<br />
a result, during high stands of sea level banks and reefs serve as a<br />
major source and sink of carbonate. During low stands of sea level,<br />
when shallow-water productivity is dramatically reduced, the locus<br />
of deposition shifts deep water. Export of carbonate from banks<br />
during high stands of sea level, after they have reached their<br />
assimilative capacity, tends to modulate these extreme conditions<br />
Because silicate is biologically active, opal flux is more<br />
governed by upper ocean productivity than is carbonate flux.<br />
Approximately 150 x 10 14 g SiO2 exit the surface ocean annually,<br />
greatest flux occurring in shelf and upwelling areas, particularly on<br />
the Antarctic shelf. Because the oceans are greatly undersaturated<br />
with respect to silicate, opal dissolution occurs both in the upper<br />
ocean and near the sea-floor. Less than one percent of the biogenic<br />
opal produced in surface waters survives in the fossil record. Higher<br />
rates of opal preservation occur in areas of high productivity, such<br />
as upwelling and Antarctic regions, whereas in oligotrophic regions<br />
nearly all the opal dissolves, resulting in little preservation in the<br />
fossil record.<br />
Montgomery, H., Pessagno, E.A.J. & Pindell,<br />
J.L. 1994. A 195 Ma Terrane in a 165 Ma Sea: Pacific Origin<br />
of the Caribbean Plate. GSA Today, 4/1, 2-6.<br />
Tectonic models purporting to describe the origin of the<br />
Caribbean plate can be divided into two broad categories conflicting<br />
on the point of in situ origin vs. genesis in the Pacific realm followed<br />
by eastward transport relative to the American plate. Important<br />
elements of Caribbean geology including Cayman Trough spreading,<br />
the presence of the Lesser Antilles and Aves volcanic arcs,<br />
incompatible crustal juxtapositions, complicated plate geometry,<br />
truncated structural trends, fossils that originated at higher<br />
latitudes, and a lengthy geologic record of eastward progression<br />
strongly suggest allochthonous origin. However, none of these is<br />
conclusive proof. The discovery of a Caribbean plate island terrane<br />
significantly older than the Caribbean Sea assures that in situ<br />
models are incorrect. The Bermeja Complex of southwestern Puerto<br />
Rico, located on the northeastern corner of the Caribbean plate,<br />
exposes Lower Jurassic chert. Deposited on a deep ocean floor,<br />
<strong>radiolaria</strong>n chert from the Bermeja is late Pliensbachian (~195 Ma)<br />
in age, predating an open marine connection between the North<br />
Atlantic and the Pacific by ~30 m.y<br />
Murchey, B.L. & Jones, D.L. 1994. The<br />
environmental and tectonic significance of two coeval<br />
Permian <strong>radiolaria</strong>n-sponge associations in eastern Oregon.<br />
In: Geology of the Blue Mountains Region of Oregon, Idaho,<br />
and Washington: Stratigraphy, Physiography, and Mineral<br />
Resources of the Blue Mountains Region. (Vallier, T.L. &<br />
Brooks, H.C., Eds.), vol. 1439. United States geological<br />
Survey, professional Paper, Report, pp. 183-198.<br />
Nakazawa, K., Ishibashi, T., Kimura, T., Koike,<br />
T., Shimizu, D. & Yao, A. 1994. Triassic<br />
biostratigraphy of Japan based on various taxa. In: Recent<br />
Development on Triassic Stratigraphy. (Guex, J. & Baud, A.,<br />
Eds.), vol. 22. Mémoires de Géologie (Lausanne), Lausanne,<br />
Switzerland. pp. 83-105.<br />
Two different faunas belonging to two different lithofacies are<br />
distinguished in the Triassic of Japan. The one belongs to the shelf<br />
facies composed of terrigenous clastic rocks, and is characterized<br />
by ammonites, bivalves, and less amount of brachiopods and<br />
gastropods. The zonation of the lower half of the Triassic is mainly<br />
based on ammonoids, while the upper half is founded on bivalve<br />
fossils. The other one belonging to the oceanic facies consists of<br />
chert, limestone, pelagic shale, and greenstone, and yields abundant<br />
conodonts and <strong>radiolaria</strong>ns. Molluscan fossils are also common in<br />
pelagic limestones. The zonation of the oceanic sequence is made by<br />
mainly conodonts and <strong>radiolaria</strong>ns The comparison of the two<br />
different zones is difficult, because the two faunas do not occur in<br />
association. Reviewing the various zonation, it becomes clear that
Radiolaria 14 Bibliography - 1994<br />
the lower Eo-Triassic Induan strata are missing both in the shelf and<br />
oceanic facies. The latest Triassic "Rhaetian" is probably lacking in<br />
the shelf facies, but developed in the oceanic facies. The shelf<br />
facies faunas are related to those of Primorye and Siberia. On the<br />
contrary, those of the oceanic facies have typical Tethyan aspects.<br />
It is worthy of note that the land plants belong to the Dictyophyllum-<br />
Clathropteris floristic province of warm climate. The present<br />
distribution of the two quite different assemblages is well explained<br />
by the plate tectonics theory.<br />
O'Dogherty, L. 1994. Middle Cretaceous Radiolaria<br />
Biochronology and Paleontology from Umbria Apennines<br />
(central Italy) and Betic Cordillera (Spain). Ph. D. Thesis.<br />
University of Lausanne, 375 p. (unpublished)<br />
A highly diversified <strong>radiolaria</strong>n fauna of middle Cretaceous age<br />
has been recovered from a detailed study of pelagic and hemipelagic<br />
sequences recording the Barremian-Turonian interval in<br />
Mediterranean Regions. Several lithologies (limestones, cherty<br />
limestones, marls and siliceous shales) in strata of selected<br />
sections with long-term sedimentary continuous succession of deepsea<br />
facies, at different localities in the Central Apennines (Apulian<br />
Block) and on the External Zones of the Betic Cordillera (Southern<br />
Iberian Paleomargin) were thoroughly examined.<br />
The taxonomy and biochronology of the middle Cretaceous<br />
Radiolaria has been studied so as to construct a precise <strong>radiolaria</strong>n<br />
zonation in the Western Mediterranean on the basis of their vertical<br />
distribution. The sequence of species in the fossil record inevitably<br />
reflects the order in which they evolved. Subsequently, this detailed<br />
biochronological analysis was used for tracing evolutionary lineages<br />
to elucidate the phylogenetic relationships of some examined taxa.<br />
Finally, generic and suprageneric classifications have been based on<br />
previous work as well as on my own analysis of the faunal<br />
succession.<br />
The biochronology has been carried out by means of Unitary<br />
Association Method (Guex 1977, 1991). A database recording the<br />
appearance of 303 species in 29 superposed horizons selected<br />
from six hundred samples of seven sections has been used to<br />
establish a sequence of 21 Unitary Associations. Each of these<br />
associations is defined by the totality of its species pair<br />
characteristics. The biochronological analysis has allowed the<br />
definition of nine new <strong>radiolaria</strong>n biochronologic units for the middle<br />
Cretaceous, each assemblage are labelled either as zones or<br />
subzones. These biochronologic units are tied to chronostratigraphy<br />
through other coexisting fossil groups, like planktonic Foraminifera<br />
and calcareous nannofossils previously studied by other authors at<br />
the same localities.<br />
Two major drastic <strong>radiolaria</strong>n faunal changes coincide with well<br />
established major Cretaceous oceanic anoxic events (OAE): early<br />
- 107 -<br />
Aptian to early Albian (OAE lA- OAE lB) and Cenomanian-Turonian<br />
boundary (OAE 2).<br />
All <strong>radiolaria</strong>n species used in the biochronology have been<br />
described with complete synonymies. They have likewise been<br />
illustrated in order to clear up the variations of their faunal spectra .<br />
Three families, 17 genera and 84 species are described as being<br />
new.<br />
Okamoto, S., Kojima, S., Suparka, S. &<br />
Supriyanto, J. 1994. Campanian (upper Cretaceous)<br />
<strong>radiolaria</strong>n from a shale clast in the Paleogene of central Java,<br />
Indonesia. J. Southeast Asian Earth Sc., 9/1-2, 45-50.<br />
A Campanian (upper Cretaceous) <strong>radiolaria</strong>n assemblage<br />
containing two new species is described from a reddish brown shale<br />
clast in a Paleogene breccia formation in the Karangsambung area,<br />
central Java, Indonesia. The occurrence of some species typically<br />
found in low paleolatitudes strongly suggests that the <strong>radiolaria</strong>ns<br />
were deposited in a tropical ocean. On the other hand, coeval<br />
Campanian <strong>radiolaria</strong>n assemblages from the blocks in the Luk-Ulo<br />
melanges, which unconformably underlies the Paleogene breccia<br />
formation, are lacking in the "tropical species" obtained from the<br />
clast in the Tertiary cover. The faunal difference indicates that the<br />
Campanian Radiolaria-bearing siliceous rocks in the Luk-Ulo<br />
melanges and Paleogene formation were deposited in different<br />
paleolatitudes and juxtaposed before the deposition of the Paleogene<br />
rocks.<br />
Wakita, K., Munasri & Bambang, W. 1994.<br />
Cretaceous <strong>radiolaria</strong>ns from the Luk Ulo Melange Complex<br />
in the Karangsambung area, central Java, Indonesia. J.<br />
Southeast Asian Earth Sc., 9/1-2, 29-43.<br />
The Luk-Ulo Melange Complex is a chaotic mixture of various<br />
kinds of sedimentary, igneous and metamorphic rocks, and is<br />
unconformably overlain by the Eocene Karangsambung Formation.<br />
Cretaceous <strong>radiolaria</strong>ns were extracted from shale and chert which<br />
are main constituents of the complex in the Karangsambung area,<br />
central Java. They are grouped into five assemblages (I-V). From the<br />
<strong>radiolaria</strong>n data, the siliceous and argillaceous rocks of the Luk-Ulo<br />
Melange Complex are considered to have been deposited in Early to<br />
Late Cretaceous time, and accreted at a subduction trench during<br />
middle to latest Cretaceous or earliest Paleocene. As the complex is<br />
unconformably overlain by the Eocene, the fragmentation and mixing<br />
of these rocks with schist and quartz porphyry must have occurred<br />
during Paleocene time.
Directory Radiolaria 14<br />
ANNOUNCEMENTS<br />
JAPANESE PUBLICATIONS<br />
Yoshiaki Aita<br />
Sakai, T. and Aita, Y. (Eds.), 1992, Proceedings of the Third Radiolarian Symposium. News<br />
of Osaka Micropaleontologists, Special Volume, No. 8, 100 p. Price: US$32 plus postage US$10<br />
(Total US$42). ISSN: 0287-0436.<br />
To order: Yoshiaki Aita<br />
Department of Geology, Faculty of General Education Utsunomiya University, Utsunomiya, 321<br />
Japan<br />
Fax (81) 286-35-31 71<br />
Ishizaki, K. and Saito, T. (Eds.), 1992, Centenary of Japanese Micropaleontology. Terra<br />
scientific Publishing Company, Tokyo, 480p. Price US$ 170 plus postage US$ 9 (Total US$<br />
179)<br />
To order: Terra Scientific Publishing Company<br />
302, 303 Jiyugaoka Komatsu Building, 24-17 Midorigaoka 2-chome, Meguro-ku, Tokyo 152,<br />
Japan<br />
Fax (81) 3-3718-4406<br />
1994 INTERRAD Calendar<br />
Paula Noble and Donna Hull<br />
Now Available: A wonderfull 1994 Calendar of Radiolaria (SEM) Photos.<br />
Featuring Radiolaria from all over the world, spanning from Devonian to Recent,<br />
contributed by scientists from Europe, North America, Asia and Australia. For<br />
Sale by the International Association of Radiolarian Paleontologists<br />
Send $ 5.00 (US $) for each calendar plus $ 1.25 postage to:<br />
Paula Noble<br />
Geology Department CSU, Sacramento<br />
CA 95819-6043 Sacramento<br />
U.S.A.<br />
Tel: (1) 916-778-6667<br />
make check payable to: INTERRAD<br />
- 108 -
Radiolaria 14 Announcements<br />
"RADREFLIB"<br />
PALEOZOIC through CENOZOIC<br />
A. Sanfilippo G.W. Renz, C.A. Nigrini and J.P. Caulet<br />
A comprehensive annotated <strong>radiolaria</strong>n reference library of all literature through 1993 -<br />
approximately 3500 entries<br />
$300-individuals, $600-departments/industry<br />
For use with NOTEBOOK & BIBLIOGRAPHY (for PCs -purchased separately from<br />
PRO/TEM) or PROCITE (for PC or Macintosh - purchased separately). The data base now<br />
includes the original library plus 2 supplements. Supplements are assembled annually and<br />
cost $50.<br />
For further information contact:<br />
Annika Sanfilippo<br />
Scripps Institution of Oceanography<br />
La Jolla, CA 92093-0220<br />
NOTE FROM THE AUTHORS: We are aware of the existence of papers, especially in the<br />
Japanese and Russian literature, but the difficulty in obtaining these papers have made it<br />
impossible to include them, since in constructing this database we have endeavored to obtain a<br />
reprint of every article included in it. At the same time we have updated Bill Riedel's reprint<br />
collection at Scripps to make it as complete as possible, so that fellow <strong>radiolaria</strong>n workers can<br />
be supplied with the latest references to pertinent <strong>radiolaria</strong>n literature. Please send your reprints<br />
to us so that we may include them in this valuable database.<br />
BIOCHRONOLOGICAL CORRELATIONS<br />
Jean Guex<br />
Spinger -Verlag DM 98 (see abstract on p. 63-64, Bibliography Section)<br />
ISBN 3-540-53937-9 ISBN 0-387-53937-9<br />
- 109 -
Directory Radiolaria 14<br />
Address Directory of Radiolarian Paleontologists<br />
Luis O'Dogherty<br />
This address directory includes members and non members of INTERRAD. We intend to present a precise<br />
directory of all people interested in any field of <strong>radiolaria</strong>n research. Please, help us to upgrade our directory by<br />
notifying any change, omission or error in this preliminary list.<br />
This is a message to everybody: please return us the included post-card, complete with your data, even if<br />
your address is OK. This will allow us to prepare a new directory including all the information requested on the<br />
postcard and this to guarantee us a good reception of Radiolaria 14.<br />
Chevron Standard Oil Company<br />
of California Library<br />
P.O. Box 5046<br />
CA 94583 San Ramon, California<br />
U.S.A.<br />
Geological Survey of Canada<br />
Cordilleran Geology Library<br />
Ms. Mary Akehurst<br />
100 W. Pender St. 5th floor<br />
V6B 1R8 Vancouver B.C.<br />
CANADA<br />
Plankton Newsletter Editor<br />
P.Hilgersom<br />
P. Higerson P.O. Box 16915<br />
1001 AK Amsterdam<br />
THE NETHERLANDS<br />
IPA International<br />
Paleontological Association<br />
Secretary-General<br />
William A. Oliver Jr.<br />
U.S. Geological Survey E-305<br />
Natural History Building<br />
20560 Washington, D.C.<br />
U.S.A.<br />
Elsevier Sc Publish., Sciences &<br />
Technology M.G. Tanke<br />
P.O. Box 330<br />
100 AH Amsterdam<br />
THE NETHERLANDS<br />
Union Oil Co. Library Technical<br />
Information Ct.<br />
376 S. Valencia Ave.<br />
CA 92621 Brea, California<br />
U.S.A.<br />
ABBASOV A. B.<br />
Akad Nauka Azerbaidzanskoi<br />
Instituta Geologii<br />
Baku<br />
AZERBAIJAN<br />
ABELMANN Andrea<br />
Wegener Institute for Polar Research<br />
Columbusstrasse - Postfach 120161<br />
D-2850 Bremerhaven<br />
GERMANY<br />
Tel: (49) 471-4831205<br />
Fax: (49) 471-4831149<br />
ADACHI Mamoru<br />
Department of Earth Sciences<br />
Faculty of Science Nagoya University<br />
464 Nagoya<br />
JAPAN<br />
AFANASIEVA Marina<br />
Aprelevka Department<br />
All-Russian Research Geological Oil<br />
Insitute (AO VNIGNI)<br />
st. Ketritsa I, Naro-Fominsk District<br />
143360 Moscow region Aprelevka<br />
RUSSIA<br />
Tel: (70) 95-4223096<br />
AGARKOV Yu. V.<br />
Rostov-on-Don University<br />
Zorge street, 40<br />
Rostov-on-Don<br />
RUSSIA<br />
AHMED Nizamuddin<br />
Geological Survey of Bangladesh<br />
153, Pioneer Road, Segunbagicha<br />
1000 Dhaka<br />
BANGLADESH<br />
AIELLO Ivano Walter<br />
Dipartimento de Scienze della Terra<br />
Universitá di Firenze. Via la Pira, 4<br />
50121 Firenze<br />
ITALY<br />
Fax: (39) 55-218628<br />
AITA Yoshiaki<br />
Department of Geology<br />
Faculty of General Education<br />
Utsunomiya University<br />
350 Mine<br />
321 Utsunomiya<br />
JAPAN<br />
Tel: (81) 286-36-1515 ext. 577<br />
Fax: (81) 286-35-3171<br />
AITCHISON Jonathan<br />
Department of Geology & Geophysics<br />
University of Sydney<br />
Edgeworth David Building<br />
NSW 2006 Sydney FO5<br />
AUSTRALIA<br />
Tel: (61) 2-692-2032<br />
Fax: (61) 2-692-0184<br />
E-mail: jona@es.su.oz.au<br />
AKERS Wilburn H.<br />
121 Maple Tree Ct.<br />
CA 90631 La Habra, California<br />
U.S.A.<br />
AKIBA Fumio<br />
JAPEX Research Center<br />
1-2-1 Hamada Mihama<br />
260 Mihama, Chiba<br />
JAPAN<br />
- 110 -<br />
AKTURK Solmaz<br />
Mobil Research & Dev. Co.<br />
P.O. Box 819047<br />
TX 75381-9047 Dallas, Texas<br />
U.S.A.<br />
ALDER Viviana A.<br />
Instituto Antártico Argentino<br />
Cerrito 1248<br />
1010 Buenos Aires<br />
ARGENTINA<br />
ALEKSEEVA Olga A.<br />
VNII Okeageologia<br />
Maklina prosp. 1<br />
190121 St. Petersburg<br />
RUSSIA<br />
ALEXANDROVICH Joanne M.<br />
Biological Oceanography<br />
Lamont-Doherty Geological<br />
Observatory Columbia University<br />
NY 10964 Palisades, New York<br />
U.S.A.<br />
AMODEO Filomena<br />
Dipartimento di Scienze della Terra<br />
Università di Napoli<br />
Largo S. Marcellino 10<br />
80138 Napoli ITALY<br />
Fax: (39) 81-5549714<br />
AMON Edward O.<br />
Institute of Geology and Geochemistry<br />
of the Urals branch<br />
Russian Academy of Sciences<br />
Pochtovyi per. 7<br />
620219 Ekaterinburg RUSSIA<br />
Tel: 3432-511997 or 519111<br />
Fax: 3432-515252<br />
ANDERSON O. Rogers<br />
Biological Oceanography<br />
Lamont-Doherty Geological<br />
Observatory Columbia University<br />
NY 10964 Palisades, New York<br />
U.S.A.<br />
E-mail: ora@ldgo.columbia.edu<br />
ANDREOLI Maria Gabriella<br />
Instituto di Zoologia<br />
Università di Parma<br />
Strada dell’Università 12<br />
43100 Parma<br />
ITALY
Radiolaria 14 Directory<br />
ARAKAWA Ryuichi<br />
Tochigi Prefectural Museum<br />
2-2 Mutsumi<br />
320 Utsunomiya<br />
JAPAN<br />
ARENDS Robert G.<br />
Unocal, Geotech Services<br />
P.O. Box 4551<br />
TX 77210-4551 Houston, Texas<br />
U.S.A.<br />
ASHBY Jeff<br />
Geological Department Victoria<br />
University Private Bag<br />
Wellington<br />
NEW ZEALAND<br />
AVERINA G. Yu<br />
Institute of Lithosphere<br />
Academy of Science<br />
Staromonethyper, 22<br />
109017 Moscow. RUSSIA<br />
Fax: (70) 95-2335590<br />
BAK Marta<br />
Institute of Geological Sciences<br />
Jagiellonian University<br />
ul. Oleandry 2a<br />
30-063 Kraków<br />
POLAND<br />
BAKER Colin<br />
McLean Laboratory<br />
MA 02543 Woods Hole, Massachuset<br />
U.S.A.<br />
BALTUCK Miriam<br />
Department of Geology<br />
Tulane University<br />
LA 70118 New Orleans<br />
U.S.A.<br />
BARBIERI Francesco<br />
Istituto de Geologia<br />
Università di Parma<br />
Viale delle Scienze 78<br />
43100 Parma ITALY<br />
Fax: (39) 521-580305<br />
BARNES Christopher R.<br />
Geological Survey of Canada<br />
580 Booth str., 20 th floor<br />
K1A OE4 Ottawa, Ontario<br />
CANADA<br />
Tel: (16) 13-9925265<br />
BARRICK James E.<br />
Department of Geosciences<br />
Texas Technical University<br />
P.O. Box 4109<br />
TX 79409 Lubbock, Texas<br />
U.S.A.<br />
BARTOLINI Annachiara<br />
Dipartimento di Sciene della Terra<br />
Universitá di Perugia<br />
Piazza dell’Universitá<br />
06100 Perugia<br />
ITALY<br />
Tel: (39) 75-5853225<br />
Fax: (39) 75-5852067<br />
BARWICZ Wanda<br />
Department of Geology<br />
Academy of Mining<br />
Al Michiewicza 30<br />
30059 Krakow<br />
POLAND<br />
BAUMGARTNER Peter O.<br />
Institut de Géologie et Paléontologie<br />
Université de Lausanne, BFSH-2<br />
CH-1015 Lausanne<br />
SWITZERLAND<br />
Tel: (41) 21-6924344<br />
Fax: (41) 21-6924305<br />
E-mail: pbaumgar@igp.unil.ch<br />
BENSON Richard<br />
Delaware Geological Survey<br />
University of Delaware<br />
DE 19716 Newark<br />
U.S.A.<br />
BERNSTEIN Renate E.<br />
5240 61st Ave South<br />
FL 33715 St. Petersburg, Florida<br />
U.S.A.<br />
BINGGAO Zhang<br />
Laboratory of Palaeobiology and<br />
Stratigraphy Nanjing Institute of<br />
Geology & Paleontology<br />
Academia Sinica<br />
Chi-Ming-Ssu<br />
210008 Nanjing CHINA<br />
Fax: (86) 25-3357026<br />
BJøRKLUND Kjell<br />
Paleontologisk Museum<br />
Oslo Universitetet<br />
Sars gate 1<br />
N-0562 Oslo 5<br />
NORWAY<br />
E-mail: kjell.bjorklund@toyen.uio.no<br />
BLOME Charles D.<br />
U.S. Geological Survey MS 919<br />
P.O. Box 25046 Federal Center<br />
CO 80225-0046 Denver, Colorado<br />
U.S.A.<br />
BLUEFORD Joyce R.<br />
Math/Science Nucleus<br />
4009 Pestana Place<br />
CA 94538-6301 Fremont, California<br />
U.S.A.<br />
BOECK Elke<br />
Institut für Paläontologie<br />
Universität Erlangen-Nürnberg<br />
Loewenichstrasse 28<br />
D-8520 Erlangen<br />
GERMANY<br />
BOERSMA Anne<br />
Microclimates 404 RRI<br />
NY 10980 Stony Point, New York<br />
U.S.A.<br />
BOLTOVSKOY Demetrio<br />
Departamento de Ciencias Biológicas<br />
Facultad de Ciencias Exactas y Naturales<br />
Universidad de Buenos Aires<br />
1428 Buenos Aires ARGENTINA<br />
Tel: (54) 1-790-9591 or 782-0620<br />
Fax: (54) 1-795-1518<br />
E-mail: postmaster@plankt.edu.ar<br />
BORISOV B.A.<br />
All-Russia Scientific Research<br />
Geological Institute (VSEGEI )<br />
Sredniy Prospect 74<br />
199026 St. Petersburg<br />
RUSSIA<br />
- 111 -<br />
BOTTAZZI MASSERA Elsa<br />
Instituto di Zoologia<br />
Università di Parma<br />
Strada dell’Università 12<br />
43100 Parma<br />
ITALY<br />
BOUNDY-SANDERS Susan<br />
1653 E Fremont Drive<br />
AZ 85282-7366 Tempe<br />
U.S.A.<br />
BOURDILLON DE GRISSAC C.<br />
Départment de Stratigraphie<br />
BP 6009<br />
45046 Orleans<br />
FRANCE<br />
BRAGIN Nikita<br />
Geological Institute of the USSR<br />
Academy of Science<br />
Pyshevsky per, 7<br />
109017 Moscow<br />
RUSSIA<br />
Tel: (70) 95-2308079<br />
BRAGINA Z.G.<br />
Geological Institute of the USSR<br />
Academy of Science<br />
Pyshevsky per, 7<br />
Moscow<br />
RUSSIA<br />
BRAUN Andreas<br />
Institut für Paläontologie der<br />
Rheinischen Friedrich-Wilhelms-<br />
Universität. Nussallee 8<br />
D-5300 Bonn 1<br />
GERMANY<br />
BRUNNER Charlotte<br />
Department of Paleontology<br />
University of California<br />
Berkeley, CA 94720<br />
U.S.A.<br />
E-mail: cbrunner@whale.st.usm.edu<br />
CACHON Jean<br />
Station Zoologique Laboratoire de<br />
Protistologie Marine<br />
06230 Villefranche-sur-Mer<br />
FRANCE<br />
CACHON Monique<br />
Station Zoologique Laboratoire de<br />
Protistologie Marine<br />
06230 Villefranche-sur-Mer<br />
FRANCE<br />
CARIDROIT Martial<br />
Université des Sciences Techniques,<br />
Lille 1 Sciences de la Terre SN 5<br />
Laboratoire de Paléontologie<br />
59655 Villeneuve d’Ascq<br />
FRANCE<br />
Tel: (33) 20-434755<br />
CARON David A.<br />
Woods Hole Oceanographic Institution<br />
MA 02543 Woods Hole, Massachuset<br />
U.S.A.<br />
CARSON Tom<br />
Geological Department<br />
Rice University<br />
P.O. Box 1892<br />
TX 77501 Houston, Texas<br />
U.S.A.
Directory Radiolaria 14<br />
CARTER Elizabeth S.<br />
58335 Timber Road<br />
OR 97064 Veronia, Oregon<br />
U.S.A.<br />
Tel: (1) 503-4292011<br />
Fax: (1) 503-4292011<br />
E-mail: I1EC@cc.pdx.edu<br />
CARTER Elizabeth S.<br />
Department of Geology<br />
Portland State University<br />
P.O. Box 1493<br />
OR 97207-8751 Portland, Oregon<br />
U.S.A.<br />
Tel: (1) 503-7254882<br />
Fax: (1) 503-4292011 or 7255900<br />
E-mail: I1EC@cc.pdx.edu<br />
CASEY Richard<br />
Marine Studies<br />
University of San Diego<br />
208 Serra Hall, Alcala Park<br />
CA 92110 San Diego, California<br />
U.S.A.<br />
Tel: (1) 619-2604600 ext 4418<br />
CASILIO Tony<br />
31 Everit Street<br />
CT 06511 New Haven, Connecticut<br />
U.S.A.<br />
CAULET Jean-Pierre<br />
Muséum National d’Histoire Naturelle<br />
Laboratoire de Géologie<br />
43, rue Buffon<br />
75005 Paris. FRANCE<br />
Tel: (33) 1-40793471 or 59<br />
Fax: (33) 1-40793739<br />
E-mail: caulet@cimrs1.mnhn.fr<br />
CHEDIYA D. M.<br />
Kand. Geol. Mineral. Nauk<br />
Tadshiskii Gosudarstrenyi Universitet<br />
Dushanbe, Tadshiskoi<br />
RUSSIA<br />
CHEN Muhong<br />
South China Sea Institute of<br />
Oceanography Academia Sinica<br />
164 West Xingang Road<br />
510301 Gangzhou<br />
CHINA<br />
CHEN Wenbin<br />
2nd Institute of Oceanographie SOA<br />
P.O. Box 1207<br />
310012 Hangzhou<br />
CHINA<br />
CHENG Yen Nien<br />
National Museum of Natural Science<br />
1 Kuan Chien Rd.<br />
40416 Taichung<br />
TAIWAN R.O.C.<br />
CHIARI Marco<br />
Dipartimento de Scienze della Terra<br />
Universitá di Firenze. Via la Pira, 4<br />
50121 Firenze. ITALY<br />
Fax: (39) 55-218628<br />
CHUVASHOV Boris I.<br />
Institute of Geology and Geochemistry<br />
of the Urals branch<br />
Academiy of Sciences<br />
Pochtovyi per. 7<br />
620219 Ekaterinburg<br />
RUSSIA<br />
CLOWES Emma<br />
Department of Geological Sciences<br />
University College London<br />
Gower Street<br />
WC1E 6BT London<br />
UNITED KINGDOM<br />
Fax: (44) 71-3887614<br />
COMBLE-DESPAQUIS Christi<br />
Université des Sciences Techniques,<br />
Lille 1 Sciences de la Terre SN 5<br />
Laboratoire de Paléontologie<br />
59655 Villeneuve d’Ascq<br />
FRANCE<br />
CONTI Maurizio<br />
Ecosystems s.a.s.<br />
Via G.F. Mariti, 10<br />
50127 Firenze ITALY<br />
Tel: (39) 55-353966<br />
Fax: (39) 55-354306<br />
COOKE James C.<br />
MEPSI Applied Stratigraphy<br />
P.O. Box 900<br />
TX 75221 Dallas, Texas<br />
U.S.A.<br />
COPESTAKE Philip<br />
BRITOIL Plc.<br />
150 St. Vincent Street<br />
G2 5LJ Glasgow, Scotland<br />
UNITED KINGDOM<br />
CORDEY Fabrice<br />
305-2336 York Avenue<br />
V6K 1C7 Vancouver B.C.<br />
CANADA<br />
CORNELL William<br />
Department of Geological Sciences<br />
University of Texas<br />
TX 79968-0555 El Paso, Texas<br />
U.S.A.<br />
Tel: (1) 915-7475501<br />
CORTESE Giuseppe<br />
Dipartimento de Scienze della Terra<br />
Universitá di Firenze. Via la Pira, 4<br />
50121 Firenze. ITALY<br />
Tel: (39) 55-2757512 or 511<br />
Fax: (39) 55-218628<br />
DANELIAN Taniel<br />
Department of Geology and Geophysiys<br />
University of Edinburgh<br />
Grat Institute, West Mains Road<br />
EH9 3JW Edinburgh<br />
UNITED KINGDOM<br />
Tel: (44) 31-6505943<br />
Fax: (44) 31-6683184<br />
E-mail: tdanelia@glg.ed.ac.uk<br />
DE WEVER Patrick<br />
CNRS- Université Pierre et Marie Curie<br />
Laboratoire de Stratigraphie T15-16 E4<br />
4 Place Jussieu<br />
F-75252 Paris Cédex 05<br />
FRANCE<br />
Tel: (33) 1-44274786<br />
Fax: (33) 1-44273831<br />
DIENI Iginio<br />
Dipartimento di Geologia,<br />
Paleontologia e Geofisica<br />
Università di Padova. Via Giotto 1<br />
35137 Padova ITALY<br />
Fax: (39) 49-8750367<br />
- 112 -<br />
DINKELMAN Menno<br />
Department of Geology<br />
Florida State University<br />
FL 32306 Tallahassee, Florida<br />
U.S.A.<br />
DONOFRIO Donato Antonio<br />
Institut für Geologie und Paläontologie<br />
Innsbruck Universität 4<br />
A-6020 Innsbruck<br />
AUSTRIA<br />
DORN Wolfgang U.<br />
Hawaii Institute of Geophysics<br />
2525 Correa Rd.<br />
HI 96822 Honolulu<br />
U.S.A.<br />
DOSZTáLY Lajos<br />
Geologisches Institut<br />
M. All. Földtani Intézet<br />
Nepstadion út 14<br />
1143 Budapest<br />
HUNGARY<br />
DOUGLAS Robert<br />
Department of Geological Sciences<br />
University of Southern California<br />
SCI-165<br />
CA 90089-0741 Los Angeles<br />
U.S.A.<br />
DOUZEN Kaori<br />
Department of Geology<br />
Faculty of Science Shimane University<br />
1060 Nishikawatsu<br />
690 Matsue<br />
JAPAN<br />
Fax: (81) 852-32-6469<br />
DRISKILL Lorinda E.<br />
9437 Fondren<br />
TX 77074 Houston, Texas<br />
U.S.A.<br />
DUMITRICA Paulian<br />
Könizstr. 39<br />
CH-3008 Bern<br />
SWITZERLAND<br />
Tel: (41) 31-3812858<br />
DUMITRICA Paulian<br />
Institut de Géologie et Paléontologie<br />
Université de Lausanne BFSH-2<br />
CH-1015 Lausanne<br />
SWITZERLAND<br />
Fax: (41) 21-6924305<br />
DUNN Dean A.<br />
Department of Geology<br />
University of Southern Mississippi<br />
MS 39406 Hattiesburg<br />
U.S.A.<br />
DYER Robin<br />
BRITOIL Plc.<br />
150 St. Vincent Street<br />
G2 5LJ Glasgow, Scotland<br />
UNITED KINGDOM<br />
EILERT Valesca Portilla<br />
Instituto de Geociencias<br />
Dept. Paleontologia<br />
Universida Rio Grande do Sul<br />
Av. Bento Goncalves 9500 , Bloco 1,<br />
Caixa Postal 15001<br />
91509-900 Porto Alegre RS<br />
BRAZIL
Radiolaria 14 Directory<br />
El KADIRI Khalil<br />
Département de Géologie<br />
Faculté des Sciences<br />
Université de Tétouan<br />
BP 2121 Tétouan<br />
MOROCCO<br />
ELLIS Glynn<br />
Institut de Géologie et Paléontologie<br />
Université de Lausanne BFSH-2<br />
CH-1015 Lausanne<br />
SWITZERLAND<br />
Tel: (41) 21-6924361<br />
Fax: (41) 21-6924305<br />
E-mail: gellis@igp.unil.ch<br />
ERBACHER Jochen<br />
Institut und Museum für Geologie und<br />
Paläontologie Universität Tübingen<br />
Sigwartstrasse 10<br />
D-72076 Tübingen<br />
GERMANY<br />
Fax: (49) 7071-296990<br />
ERNST Charlene Snow<br />
College of Oceanography<br />
Oceanograpy Administration Building<br />
104 Oregon State University<br />
OR 97331-5503 Corvallis, Oregon<br />
U.S.A.<br />
EZAKI Yoichi<br />
Dept. of Geosciences. Faculty of<br />
Sciences. Osaka City University<br />
Sugimoto 3-3-138<br />
558 Sumiyoshi-ku, Osaka<br />
JAPAN<br />
Fax: (81) 6-605-2604 or 2522<br />
FARIDUDDIN Mohammad<br />
Department of Geology<br />
Northern Illinois University<br />
IL 60115 Dekalb, Illinois<br />
U.S.A.<br />
FEARY David<br />
Department of Geology<br />
Australian National University<br />
P.O. Box 4<br />
ACT 2600 Canberra<br />
AUSTRALIA<br />
FEBVRE Jean<br />
Station Zoologique<br />
Laboratoire de Protistologie Marine<br />
06230 Villefranche-sur-Mer<br />
FRANCE<br />
FEBVRE-CHEVALIER Colette<br />
Station Zoologique Laboratoire de<br />
Protistologie Marine<br />
06230 Villefranche-sur-Mer<br />
FRANCE<br />
FENG Qinlay<br />
Geology Department<br />
China University of Geosciences<br />
430074 Wuhan City, Hubei Province<br />
CHINA<br />
FLOREZ-ABIN Emiliano<br />
Centro de Investigaciones Geológicas<br />
Oficios 154, Teniente Rey y Amargura<br />
Ciudad de la Habana<br />
CUBA<br />
FLUEGEMAN Rich<br />
Department of Geology Ball State<br />
IN 47306 Munsie<br />
U.S.A.<br />
FOLK Robert L.<br />
Department of Geological Sciences<br />
University of Texas at Austin<br />
P.O. Box 7909<br />
TX 78713-7909 Austin, Texas<br />
U.S.A.<br />
FORDHAM Barry G.<br />
Geological Survey<br />
Regional Investigations<br />
Queensland Department of Mines<br />
GPO Box 194<br />
4001 Brisbane, QLD<br />
AUSTRALIA<br />
FRIEND Jennifer<br />
95 Water Lane<br />
Oakington, Cambs.<br />
UNITED KINGDOM<br />
FUNAKAWA Satoshi<br />
Dept. of Geoscience. Faculty of<br />
Sciences. Osaka City University<br />
Sugimoto 3-3-138<br />
558 Sumiyoshi-ku, Osaka<br />
JAPAN<br />
Fax: (81) 6-605-2604 or 2522<br />
FURUTANI Hiroshi<br />
Hyogo Museum of Natural and<br />
Environmental Sciences<br />
6 Yayoigaoka, Sanda<br />
669-13 Hyogo<br />
JAPAN<br />
GOLL Robert<br />
IKU Institute for kontinental<br />
sokkelunderwsokelser<br />
petroleumsteknologi A/S<br />
Hakon Magnussonsgt 1B P.O.Box 1883<br />
N-7002 Jarelles, Trondheim<br />
NORWAY<br />
Tel: (47) 7-9200611 ext. 149<br />
GOLTMAN E. V.<br />
Institute of Geology Academia of<br />
Sciences<br />
Stalinbad, Dushnabe<br />
TADZHIKISTAN<br />
GOMBOS A.<br />
Exxon Production Research<br />
P.O. Box 2189<br />
TX 77001 Houston, Texas<br />
U.S.A.<br />
GORBOVETS A. N.<br />
Siberian Scientific Research<br />
Krasnyi pr. 80<br />
Novosibirsk<br />
RUSSIA<br />
GORBUNOV V.S.<br />
Institute of Geological Sciences<br />
Academia of Sciences<br />
Chkalova, 58-b<br />
54 Kiev<br />
UKRAINE<br />
GORICAN Spela<br />
Paleontoloski Institut Ivana Rakovca<br />
ZRC SAZU<br />
Gosposka 13<br />
61000 Ljubljana<br />
SLOVENIA<br />
Tel: (386) 61-1256068<br />
Fax: (386) 61-1255253<br />
E-mail: spela.gorican@uni-lj.si<br />
- 113 -<br />
GóRKA Hanna<br />
Iniwerytet Warszawski Wydzial<br />
Geologii Instytut Geologii<br />
Podstawowej<br />
Al. Zwirki i Wigury 93<br />
02-089 Warsaw<br />
POLAND<br />
TEL: (48)-22-223051<br />
GOURMELON Françoise<br />
Laboratoire de Paléontologie et de<br />
Stratigraphie du Paleozoique<br />
Facuté des Sciences<br />
Université de Bretagne Occidentale<br />
6, Avenue le Gorgeu<br />
29283 Brest, Cedex<br />
FRANCE<br />
GOWING Marcia<br />
Institute of Marine Sciences<br />
University of California<br />
CA 95064 Santa Cruz, California<br />
U.S.A.<br />
E-mail: gowing@cats.ucsc.edu<br />
GRANLUND Anders<br />
Geologisk Institut<br />
Kungstensgatan 45<br />
S-10691 11386 Stockholm<br />
SWEDEN<br />
GREENE Malcolm B.<br />
13714 Lynnwood Ln<br />
TX 77478 Sugar Land, Texas<br />
U.S.A.<br />
GRIGORJEVA Ali<br />
Ural Geological Department<br />
Veinera 55<br />
Sverdlovsk<br />
RUSSIA<br />
GUERRA Rudy<br />
Mobil Exploration & Production<br />
P.O. Box 900<br />
TX 75221 Dallas, Texas<br />
U.S.A.<br />
GUEX Jean<br />
Institut de Géologie et Paléontologie<br />
Université de Lausanne. BFSH-2<br />
CH-1015 Lausanne<br />
SWITZERLAND<br />
Tel: (41) 21-6924346<br />
Fax: (41) 21-6924305<br />
E-mail: jguex@igp.unil.ch<br />
GUPTA Shyam Murti<br />
Geological Oceanography National<br />
Institute of Oceanography<br />
403 004 Dona Paula, Goa<br />
INDIA<br />
GURSKY Hans-Jürgen<br />
Geologisch Paläontologisches Institut<br />
TH Darmstadt<br />
Schnittspahustrasse 9<br />
D-64287 Darmstadt<br />
GERMANY<br />
GUTSCHICK Raymond C.<br />
2901 Leonard<br />
OR 97504 Medford, Oregon<br />
U.S.A.
Directory Radiolaria 14<br />
HADA Shigeki<br />
Department of Geology<br />
Faculty of Science Kochi University<br />
780 Akebono-cho, Kochi<br />
JAPAN<br />
Tel: (81) 888-44-0111<br />
Fax: (81) 888-43-4220<br />
HAQUE M.D. Ershadul<br />
Geological Survey of Bangladesh<br />
153, Pioneer Road, Segunbagicha<br />
1000 Dhaka<br />
BANGLADESH<br />
HARPER Gregory<br />
Department of Geological Sciences<br />
State University of New York<br />
NY 12222 Albany, New York<br />
U.S.A.<br />
HASHIMOTO Hisao<br />
88 Tsuji<br />
Otera Itano-cho, Itano-gun<br />
779-01 Tokushima<br />
JAPAN<br />
HASLETT Simon K.<br />
Marine Geoscience Research Group<br />
Department of Geology<br />
University of Wales Cardiff<br />
P.O. Box 914<br />
CF1 3YE Cardiff<br />
UNITED KINGDOM<br />
HASSAN Nagib<br />
Geological Survey of Bangladesh<br />
153, Pioneer Road, Segunbagicha<br />
1000 Dhaka<br />
BANGLADESH<br />
HATTORI Isamu<br />
Geological Laboratory<br />
Fukui University<br />
910 Fukui<br />
JAPAN<br />
HAYS James<br />
Lamont-Doherty Geological<br />
Observatory Columbia University<br />
NY-10964 Palisades, New York<br />
U.S.A.<br />
HAYS Patricia<br />
College of Oceanography<br />
Oceanograpy Administration Building<br />
104 Oregon State University<br />
OR 97331-5503 Corvallis, Oregon<br />
U.S.A.<br />
HEIN James R.<br />
U.S. Geological Survey<br />
345 Middlefield Road<br />
CA 94025 Menlo Park, California<br />
U.S.A.<br />
HERMELIN Otto<br />
Department of Geology University of<br />
Stockholm<br />
S-10691 Stockholm<br />
SWEDEN<br />
HEYROTH Paul D.<br />
Program in Geosciences University of<br />
Texas at Dallas<br />
P.O. Box 830688<br />
75083-0688 Richardson, Texas<br />
U.S.A.<br />
Tel: (1) 2146902401<br />
Fax: (1) 2146902537<br />
HILL P. H.<br />
Waitaki Catchment Commission<br />
Kurow<br />
NEW ZEALAND<br />
HIRAISHI Mikiko<br />
Department of Geosciences Faculty of<br />
Sciences Oska City University<br />
Sugimoto 3-3-138<br />
558 Sumiyoshi, Osaka<br />
JAPAN<br />
Fax: (81) 6-605-2604 or 2522<br />
HISADA Ken Ichiro<br />
Institute of Geoscience<br />
University of Tsukuba<br />
Tennoudai 1-1-1<br />
305 Tsukuba, Ibaraki<br />
JAPAN<br />
HOBAN Michael<br />
Department of Geology<br />
Golden State Park<br />
CA 94118 San Francisco, California<br />
U.S.A.<br />
HOLDSWORTH Brian K.<br />
Department of Geology<br />
University of Keele<br />
ST5 5BG Keele, Staffordshire<br />
UNITED KINGDOM<br />
HOLLANDE André<br />
Faculté des Sciences. Paris VI<br />
Evolution des Etres Organisés<br />
105 bd. Raspail<br />
Paris<br />
FRANCE<br />
HOLLIS Christopher John<br />
Department of Geology<br />
University of Auckland<br />
Private Bag, Auckland 1<br />
NEW ZEALAND<br />
HOLZER Hans Ludwig<br />
Institut für Geologie und Paläontologie<br />
Universität Graz<br />
Heinrichstrasse 26<br />
A-8010 Graz<br />
AUSTRIA<br />
HONJO Susumo<br />
Woods Hole Oceanographic Institution<br />
MA 02543 Woods Hole, Massachuset<br />
U.S.A.<br />
HORI Rie<br />
Faculty of General Education<br />
Department of Earth Science<br />
Ehime University<br />
Bunkyo-cho 3<br />
790 Matsuyama<br />
JAPAN<br />
HULL MEYERHOFF Donna<br />
Program in Geosciences<br />
University of Texas at Dallas<br />
P.O. Box 830688<br />
75083-0688 Richardson, Texas<br />
U.S.A.<br />
Tel: (1) 214-6902475<br />
Fax: (1) 214-6902537<br />
E-mail: dmhull@utdallas.edu<br />
- 114 -<br />
IAMS William J.<br />
Department of Earth Sciences<br />
Sir Wilfred Grenfell College<br />
Memorial University<br />
A2H 6P9 Corner Brook, Newfoundland<br />
CANADA<br />
Tel: (17) 09-6862764<br />
ICHIKAWA Koichiro<br />
Department of Geosciences Faculty of<br />
Sciences Osaka City University<br />
Sugimoto 3-3-138<br />
558 Sumiyoshi-ku, Osaka<br />
JAPAN<br />
Fax: (81) 6-605-2604 or 2522<br />
IGO Hisaharu<br />
Dept. of Astronomy and Earth Sciences<br />
Tokyo Gakugei University<br />
4-1-1 Nukui Kita-Machin<br />
184 Koganei, Tokyo<br />
JAPAN<br />
IGO Hisayoshi<br />
Instiitute of Geoscience<br />
University of Tsukuba<br />
305 Ibaraki<br />
JAPAN<br />
IIJIMA Azuma<br />
Geological Institute<br />
University of Tokyo<br />
7-3-1 Hongo<br />
113 Tokyo<br />
JAPAN<br />
IMAZATO Akihiko<br />
Pasco Corporation<br />
Yokohama Branch Office<br />
Miki Bldg. 1-1-3 Hiranuma Nishi-ku<br />
220 Yokohama<br />
JAPAN<br />
IMOTO Nobuhiro<br />
Department of Earth Sciences Kyoto<br />
University of Education<br />
Fukakusa Fushimi-ku<br />
612 Kyoto<br />
JAPAN<br />
INGLE James<br />
Department of Geology<br />
Stanford University<br />
CA 94305 Stanford, California<br />
U.S.A.<br />
ISHIDA Keisuke<br />
Department of Earth Sciences College<br />
of General Education<br />
University of Tokushima<br />
1-1 Minamijosanjima-cho<br />
770 Tokushima<br />
JAPAN<br />
ISHIDA Kotaro<br />
Department of Geology Faculty of<br />
Science Shimane University<br />
1060 Nishikawatsu<br />
690 Matsue JAPAN<br />
Fax: (81) 852-32-6469<br />
ISHIGA Hiroaki<br />
Department of Geology<br />
Faculty of Science Shimane University<br />
1060 Nishikawatsu<br />
690 Matsue JAPAN<br />
Tel: (81) 852-32-6459<br />
Fax: (81) 852-32-6469<br />
E-mail: g01483@sinet.ad.jp
Radiolaria 14 Directory<br />
ISOZAKI Yukio<br />
Earth and Planetary Sciences<br />
Tokyo Institute of Technology<br />
152 Meguro, Tokyo<br />
JAPAN<br />
ISVEKOV I.N.<br />
Institute of Lithosphere<br />
Staromonetny per. 22<br />
Moscow<br />
RUSSIA<br />
ITASAKA Koji<br />
Department of Geology and<br />
Mineralogy Faculty of Science<br />
Niigata University<br />
950-21 Niigata<br />
JAPAN<br />
IVIATUL A.G.<br />
Institute Oceanology<br />
Academy of Sciences<br />
Krasikova 23<br />
117218 Moscow<br />
RUSSIA<br />
IWASAKI Masao<br />
OYO Corporation Tokushima Branch<br />
Sako 5-Bancho, 10-3<br />
770 Tokushima<br />
JAPAN<br />
IWATA Keiji<br />
Geological Survey of Hokkaido<br />
N18 W12<br />
060 Sapporo<br />
JAPAN<br />
JANIN Marie-Christine<br />
27, Rue de Clignancourt<br />
75018 Paris<br />
FRANCE<br />
JOHNSON D.A.<br />
Woods Hole Oceanographic Institution<br />
MA 02543 Woods Hole, Massachuset<br />
U.S.A.<br />
JOHNSON Thomas<br />
Department of Geology<br />
University of Minneapolis<br />
108 Pillsbury Hall<br />
MI 55455 Minneapolis<br />
U.S.A.<br />
JUD Ruth<br />
Könizstr. 39<br />
CH-3008 Bern<br />
SWITZERLAND<br />
KAKUWA Yoshitaka<br />
Department of Earth Sciences &<br />
Astronomy College of Arts & Sciences<br />
University of Tokyo at Komaba<br />
3-8-1 komaba, Meguro-ku<br />
153 Tokyo<br />
JAPAN<br />
KAMATA Yoshihito<br />
Institute of Geoscience<br />
University of Tsukuba<br />
Tennoudai 1-1-1<br />
305 Tsukuba, Ibaraki<br />
JAPAN<br />
KASHIMA Naruhiko<br />
Department of Geology<br />
Faculty of General Education<br />
Ehime University<br />
Bunkyo-cho 3<br />
790 Matsuyama<br />
JAPAN<br />
KATO Yukihiro<br />
Institute of Continental Shelf Survey<br />
Hydrographic Department<br />
Maritime Safety Agency<br />
3-1, Tsukiji 5-Chome, Chuo-ku<br />
104 Tokyo. JAPAN<br />
Tel: (81) 3-5413811 or 3819<br />
KAWABATA Kiyoshi<br />
Osaka Museum of Natural History<br />
Nagai Park Higashi-sumiyoshi-ku<br />
546 Osaka<br />
JAPAN<br />
KAZINTSOVA Ludmila I.<br />
All-Russia Scientific Research<br />
Geological Institute (VSEGEI )<br />
Sredniy Prospect 74<br />
199026 St. Petersburg<br />
RUSSIA<br />
KELLOG Davida<br />
Institute of Quaternary Studies<br />
University of Maine<br />
ME 04469 Orono, Maine<br />
U.S.A.<br />
KEMKIN Igor V.<br />
Far Eastern Geological Institute<br />
Russian Academy of Science<br />
159 Prospect, 100 - Letiya<br />
690022 Vladivostok<br />
RUSSIA<br />
KESTNER F.F.<br />
Central Laboratory<br />
Ministry of Geology. Engelsa 86<br />
84 Tashkent<br />
RUSSIA<br />
KHABAKOV A.V.<br />
All-Russia Scientific Research<br />
Geological Institute (VSEGEI )<br />
Sredniy Prospect 74<br />
199026 St. Petersburg<br />
RUSSIA<br />
KHOKHLOVA Irina Ye<br />
Geologocal Institute<br />
Academy of Sciences<br />
Pyshevsky per, 7<br />
109017 Moscow RUSSIA<br />
Tel: (70) 95-2308079<br />
KIDO Satishi<br />
Tsurga H.S.<br />
24-1-3 Akasaki<br />
914-02 Tsurga City, Fuki Prefecture<br />
JAPAN<br />
KIESSLING Wolfgang<br />
Institut für Paläontologie<br />
Universität Erlangen-Nürnberg<br />
Loewenichstrasse 28<br />
D-8520 Erlangen<br />
GERMANY<br />
KILMAR N.<br />
5260 Angeles Crest<br />
CA 91011 La Canada, California<br />
U.S.A.<br />
- 115 -<br />
KITO Norio<br />
Institute of Earth Science<br />
College of General Education<br />
Hokkaido University of Education<br />
1-2 Hachiman-cho<br />
040 Hakodate<br />
JAPAN<br />
Tel: (81) 0138-41-1121<br />
Fax: (81) 0138-42-3982<br />
KLEIN George de V.<br />
University of Illinois 245<br />
Natural History Building<br />
1301 W. Green Street<br />
IL 61801-2999 Urbana, Illinois<br />
U.S.A.<br />
KLING S.A.<br />
416 Shore View Lane<br />
CA 92024 Leucadia, California<br />
U.S.A.<br />
KNIPPER A.I.<br />
Geological Institute of the USSR<br />
Academy of Science<br />
Pyzhenwski per 7<br />
109017 Moscow<br />
RUSSIA<br />
Tel: (70) 95-2308079<br />
KOIZUMI Itaru<br />
Osaka University<br />
1-1 Machikaneyama-cho Toyonaka-shi<br />
560 Osaka<br />
JAPAN<br />
KOJIMA Satoru<br />
Department of Earth Sciences Faculty<br />
of Sciences Nagoya University<br />
464-01 Chikusa, Nagoya<br />
JAPAN<br />
KOLAR-JURKOVSEK Tea<br />
Geoloski Zavod Ljubljana<br />
Dimiceva 14<br />
61000 Ljubljana<br />
SLOVENIA<br />
Tel: (386) 61-315044<br />
KOLETTI Lida<br />
Ifaistou 13<br />
14565 Ekaly, Athens<br />
GREECE<br />
KONEVA M.P.<br />
Institute of Tectonics & Geophysics<br />
Far East Branch of the Russian<br />
Academy of Sciences<br />
65 Kim Yu Chena Street<br />
680063 Khabarovsk<br />
RUSSIA<br />
KOSAKA Yuko<br />
Department of Geology<br />
Faculty of Science<br />
Shimane University<br />
690 Matsue<br />
JAPAN<br />
KOTZIAN Sonia Bender<br />
Instituto de Geociencias<br />
Dept. Paleontologia<br />
Universida Rio Grande do Sul<br />
Av. Bento Goncalves 9500 , Bloco 1,<br />
Caixa Postal 15001<br />
91509-900 Porto Alegre RS<br />
BRAZIL
Directory Radiolaria 14<br />
KOUTSOUKOS Eduardo A.M.<br />
Petroleo Brasileiro S.A.<br />
(PETROBRAS) CENPES, Cidade<br />
Universitaria<br />
Q7, CEP 21910<br />
Ilha do Fundáo, Rio do Janeiro<br />
BRAZIL<br />
KOZLOVA Genrietta E.<br />
All-Russian Petroleum Scientific<br />
Research Geological Exploration<br />
Institute VNIGNI<br />
Micropaleontological Laboratory<br />
Liteynii propect 39<br />
191104 St. Petersburg<br />
RUSSIA<br />
Tel: (78) 12- 2780028<br />
KOZUR Heinz<br />
Rèzsú u. 83<br />
H-1029 Budapest<br />
HUNGARY<br />
KRIMSALOVA V.T.<br />
Geological Survey<br />
Proletar street, 11<br />
685000 Magadan<br />
RUSSIA<br />
KRSINIC Franco<br />
Biological Institute<br />
50000 Dubrovnik<br />
CROATIA<br />
KRUGLIKOVA Svetlana B.<br />
Institute Oceanology<br />
Academy of Sciences<br />
Krasikova 23<br />
117 218 Moscow<br />
RUSSIA<br />
KRYLOV K. Arturovich<br />
Geological Institute<br />
Russian Academy of Sciences<br />
Pyzhevski per. 7<br />
109017 Moscow<br />
RUSSIA<br />
KUMON Fujio<br />
Faculty of Science<br />
Shinshu University<br />
390 Matsumoto, Nagano<br />
JAPAN<br />
KURIMOTO Chikao<br />
Geology Department<br />
Geological Survey of Japan<br />
1-1-3 Higashi<br />
305 Tsukuba, Ibaraki<br />
JAPAN<br />
KUWAHARA Kiyoko<br />
Department of Geoscience Faculty of<br />
Sciences Osaka City University<br />
Sugimoto 3-3-138<br />
558 Sumiyoshi-ku, Osaka<br />
JAPAN<br />
Fax: (81) 6-605-2604 or 2522<br />
LABESSE Bernard<br />
Laboratoire de Géologie<br />
Ecole Normale Supérieur de Saint-Cloud<br />
Avenue de la Grille d’Honneur<br />
Parc de Saint-Cloud<br />
92211 Saint-Cloud<br />
FRANCE<br />
LABRACHERIE Monique<br />
Département de Géologie et<br />
Oceanographie<br />
Université de Bordeaux<br />
Avenue des Facultés<br />
F-33405 Talence Cedex<br />
FRANCE<br />
LAMBERT B.<br />
Centre Scientifique et Technique<br />
Groupe Total<br />
Compagnie Française des Pétroles<br />
Domaine de Beauplan - Rte de Versailles<br />
78470 St-Rémy- Lès-Chevreuse<br />
FRANCE<br />
LAZARUS David B.<br />
Geological Institute<br />
ETH-Zentrum<br />
Sonneggstrasse 5<br />
CH-8092 Zürich<br />
SWITZERLAND<br />
Tel: (41) 1-6325695<br />
Fax: (41) 1-6320819<br />
E-mail: gonzo@erdw.ethz.ch<br />
LEFFINGWELL Harry<br />
Union Oil Co.<br />
Sciences & Technology Division<br />
376 S. Valencia Avenue<br />
CA 92621 Brea, California<br />
U.S.A.<br />
LEVENTER Amy R.<br />
Byrd Polar Research Center<br />
Ohio State University<br />
125 South Oval Mall<br />
OH 43210-1308 Columbus, Ohio<br />
U.S.A.<br />
E-mail:<br />
rschere@ohstmvsa.acs.ohio-state.edu<br />
LING Hsin Yi<br />
Northern Illinois University<br />
Department of Geology<br />
1527 Pickwick Ln.<br />
IL 60115-2854 DeKalb, Illinois<br />
U.S.A.<br />
LIPMAN Raissa K.<br />
Novosibirskaja St. 13, Flat 77<br />
197342 St. Petersburg<br />
RUSSIA<br />
LIPPS Jere H.<br />
Department of Geology<br />
University of California<br />
CA 95616 Davis, California<br />
U.S.A.<br />
E-mail: jlipps@ucmp1.berkeley.edu<br />
LITVINOVA NataliyaN.<br />
Kamchatgeologia<br />
Street Mischennaya, 106<br />
683016 Petropavlovsk-Kamchatstky<br />
RUSSIA<br />
LLORENTE BOUSQUETS J.<br />
Museo de Zoología Universidad<br />
Autónoma de Mexico (UNAM)<br />
20 D.F. CD Universidad. Ap. 70-399<br />
04510 Mexico D.F.<br />
MEXICO<br />
LOMBARI Gail<br />
20 Knight Street<br />
RI 02816 Coventry<br />
U.S.A.<br />
- 116 -<br />
LONG Donna M.<br />
Department of Earth Sciences<br />
Monash University<br />
3168 Clayto, Victoria<br />
AUSTRALIA<br />
LORD Alan Richard<br />
Department of Geological Sciences<br />
University College London<br />
Gower Street<br />
WC1E 6BT London<br />
UNITED KINGDOM<br />
Tel: (44) 71-3807131<br />
Fax: (44) 71-3887614<br />
LOZANO José<br />
Departamento de Geología<br />
Universidad Nacional Bogota S.A.<br />
COLUMBIA<br />
LOZYNYAK Peter Yu<br />
Ukraina NKGI<br />
Mitskevicha sq. 8<br />
290601 Lvov<br />
UKRAINE<br />
LUCZKOWSHA E.<br />
Akademia Gornicizo<br />
Hutnicza Katedra Paleontologii<br />
Al Michiewicza 30<br />
30059 Krakow<br />
POLAND<br />
LUKANINA Irena B.<br />
Institut de Recherches Scientifiques<br />
CEBMOPTEO BNI Oceanologie D 120<br />
190 120 St. Petersburg<br />
RUSSIA<br />
LUKKE Donald<br />
7721 El Padre<br />
TX 75248 Dallas, Texas<br />
U.S.A.<br />
MAC LEOD Norman<br />
Department of Geological Sciences<br />
University College London<br />
Gower Street<br />
WC1E 6BT London<br />
UNITED KINGDOM<br />
Fax: (44) 71-3887614<br />
MALLAN-DALLA PIAZZA Pascale<br />
Institut de Géologie et Paléontologie<br />
Université de Lausanne. BFSH-2<br />
CH-1015 Lausanne<br />
SWITZERLAND<br />
Tel: (41) 21-6924362<br />
Fax: (41) 21-6924305<br />
E-mail: Pascale.DallaPiazza@igp.unil.ch<br />
MAMEDOV N.A.<br />
A. Azizbekov Institute of Oil<br />
Baku<br />
AZERBAIJAN<br />
MARCUCCI-PASSERINI Marta<br />
Dipartimento de Scienze della Terra<br />
Universitá di Firenze. Via la Pira, 4<br />
50121 Firenze ITALY<br />
Tel: (39) 55-2757512 or 511<br />
Fax: (39) 55-218628<br />
MARIANOS Andrew W.<br />
Exxon Co. USA<br />
P.O. Box 4279<br />
TX 77001 Houston, Texas<br />
U.S.A.
Radiolaria 14 Directory<br />
MAROLT Richard<br />
Chevron Oil Inc.<br />
P.O. Box 446<br />
Ca 90631 La Habra, California<br />
U.S.A.<br />
MARTIN H.A.<br />
School of Botany University of NSW<br />
P.O. Box 1<br />
NSW 2033 Kensington<br />
AUSTRALIA<br />
MARTIN Richard<br />
780 Oak Grove Road B. 318<br />
CA 94518 Concord, California<br />
U.S.A.<br />
MARTY Richard<br />
780 Oak Grove Rd. B318<br />
CA 94518 Concord, California<br />
U.S.A.<br />
MASSE J. P.<br />
Centre de Sédimentologie et de<br />
Paléontologie C.N.R.S.-U.R.A. 1208<br />
Université de Provence-St.-Charles<br />
3, Place Victor-Hugo - Case 67<br />
13331 Marseille Cédex 3<br />
FRANCE<br />
MATSUOKA Atsushi<br />
Department of Earth Sciences<br />
College of General Education<br />
Niigata University<br />
Ikarashi 2 no cho 8050<br />
950-21 Niigata<br />
JAPAN<br />
Tel: (81) 25-262-6376<br />
Fax: (81) 25-262-7278<br />
MATUL Alexander<br />
Institute Oceanology<br />
Academy of Sciences<br />
Krasikova 23<br />
117218 Moscow<br />
RUSSIA<br />
McMILLEN Ken<br />
Gulf Oil Exploration & Production Co.<br />
P.O. Box 1392<br />
CA 93302 Bakersfield, California<br />
U.S.A.<br />
MERINFELD G.<br />
Department of Oceanography<br />
Dalhouise University<br />
B3H 4J1 Halifax, N.S.<br />
CANADA<br />
MITSUSIO Taikou<br />
Department of Geology<br />
Kochi University<br />
780 Akebono, Kochi<br />
JAPAN<br />
MIZIK M.<br />
Department of Geology & Paleontology<br />
Faculty of Natural Sciences<br />
J. A. Comenius University<br />
Mlynska Dolina Pav. G1<br />
842 12 Bratislav<br />
SLOVAKIA<br />
MIZUTANI Shinjiro<br />
Department of Earth Sciences<br />
Faculty of Sciences<br />
Nagoya University<br />
464-01 Chikusa, Nagoya<br />
JAPAN<br />
MOHAMMAD Fariduddin<br />
Department of Geology<br />
Northern Illinois University<br />
IL 60115-2854 Dekalb<br />
U.S.A.<br />
MOKSYAKOVA A.M.<br />
All-Union Petroleum Scientific<br />
Research Institute of Geology<br />
Caasussee Entusiastov 124<br />
Moscow<br />
RUSSIA<br />
MOLINA-CRUZ Adolfo<br />
Instituto de Ciencias del Mar<br />
Universidad Autónoma de Mexico<br />
(UNAM) Ciudad Universitaria<br />
04510 Mexico D.F.<br />
MEXICO<br />
MOORE Ted<br />
Exxon Production Research PTS-1663<br />
P.O. Box 2189<br />
TX 77001 Houston, Texas<br />
U.S.A.<br />
E-mail: ted.moore@um.cc.umich.edu<br />
MORIN Karen M.<br />
2016 Wedgewood Lane<br />
TX 75006 Carrollton, Texas<br />
U.S.A.<br />
MORLEY Joe J.<br />
32 West End Ave.<br />
NJ 07675 Westwood<br />
U.S.A.<br />
E-mail: morley@ldgo.columbia.edu<br />
MOSTLER Helfried<br />
Institut für Geologie und Paläontologie<br />
Universität Innsbruck<br />
Innrain 52<br />
A-6020 Innsbruck<br />
AUSTRIA<br />
MOTOYAMA Isao<br />
Geological Survey of Japan<br />
1-1-3 Higashi<br />
305 Tsukuba, Ibaraki<br />
JAPAN<br />
MULVANE Sonja<br />
Shell Oil Co.<br />
P.O. Box 481<br />
TX 77001 Houston, Texas<br />
U.S.A.<br />
MURATA Masafumi<br />
Department of Geology Faculty of<br />
Sciences Kumamoto University<br />
860 Kumamoto<br />
JAPAN<br />
MURCHEY Benita L.<br />
U.S. Geological Survey<br />
Paleontological Branch, MS 915<br />
Middlefield Road 345<br />
94025 Menlo Park, California<br />
U.S.A.<br />
Tel: (1) 415-3294980<br />
Fax: (1) 415-3294975<br />
E-mail: bmurchey@usgs.gov<br />
MURRAY Dave<br />
Department of Geological Sciences<br />
Brown University<br />
P.O. Box 1846<br />
RI 02912 Providence<br />
U.S.A.<br />
- 117 -<br />
MUZAVOR Sadat<br />
Seminario Aquacultura<br />
Universidae doAlgarve<br />
Campo de Gambelas, Apartado 322<br />
8004 Faro<br />
PORTUGAL<br />
Tel: (35) 189-29761 or 28177<br />
NAGAI Hiromi<br />
Furukawa Museum Dating and<br />
Materials Research Center<br />
Nagoya University<br />
Chikusa-ku<br />
464-01 Nagoya<br />
JAPAN<br />
NAGATA Kyoichi<br />
Technical Laboratory Japanese<br />
Petroleum Exploration Ltd.<br />
3-5-5 Midorigaoka Hamura-machi<br />
Nishitama-gun<br />
190-11 Tokyo<br />
JAPAN<br />
NAKAE Satoshi<br />
Kyushu Center<br />
Geological Survey of Japan<br />
2-1-28 Shiobara<br />
815 Minami, Fukuoka<br />
JAPAN<br />
NAKAGAWA Cuzo<br />
Geological Institute<br />
Tokushima University<br />
770 Kjoikugakubu, Tokushima<br />
JAPAN<br />
NAKAGAWA Mitjuro<br />
Department of Geology & Mineralogy<br />
Faculty of Science<br />
Hokkaido University<br />
060 Sapporo, Hokkaido<br />
JAPAN<br />
NAKASEKO Kojiro<br />
Kobe Yamate Women’s College<br />
3 Suwayama<br />
650 Chuo, Kobe<br />
JAPAN<br />
NIGRINI Catherine<br />
510 Papyrus Drive<br />
CA 90631 La Habra, Heights<br />
U.S.A.<br />
Tel: (1) 213-6978842<br />
E-mail:74710.2367@compuserve.com<br />
NISHIMURA Akiko<br />
3212 Satoyamabe<br />
390-02 Matsumoto, Nagano<br />
JAPAN<br />
NISHIMURA Harumi<br />
Institute of Geoscience<br />
University of Tsukuba<br />
Tennoudai 1-1-1<br />
305 Tsukuba, Ibaraki<br />
JAPAN<br />
NISHIMURA Kouichi<br />
Department of Geology<br />
Faculty of Sciences Shimane University<br />
1060 Nishikawatsu<br />
690 Matsue, Shimane<br />
JAPAN<br />
Fax: (81) 852-32-6469
Directory Radiolaria 14<br />
NISHIWAKI Niichi<br />
Faculty of Social Research<br />
Nara University<br />
631 Nara<br />
JAPAN<br />
NISHIYAMA Yukio<br />
Institute of Geoscience<br />
Doctoral Program of Geoscience<br />
The University of Tsukuba<br />
Tennoudai 1-1-1<br />
305 Tsukuba, Ibaraki<br />
JAPAN<br />
NOBLE Paula<br />
Geology Department CSU, Sacramento<br />
CA 95819-6043 Sacramento<br />
U.S.A.<br />
Tel: (1) 916-778-6667<br />
NOGAMI Yasuo<br />
1-5-12, Suzaku<br />
631 Nara<br />
JAPAN<br />
O’DOGHERTY Luis<br />
Institut de Géologie et Paléontologie<br />
Université de Lausanne BFSH-2<br />
CH-1015 Lausanne<br />
SWITZERLAND<br />
Tel: (41) 21-6924360<br />
Fax: (41) 21-6924305<br />
E-mail: lodogher@igp.unil.ch<br />
OBRADOVIC Jelena<br />
Faculty of Mining & Geology<br />
University of Beograd<br />
Djusina 7<br />
11000 Beograd<br />
YUGOSLAVIA<br />
OGAWA Yujiro<br />
Institute of Geosciences<br />
University of Tsukuba<br />
Tennoudai 1-1-1<br />
305 Tsukuba, Ibaraki<br />
JAPAN<br />
OHNENSTTETER Maryse<br />
C.N.R.S. Centre de Recherches sur la<br />
Synthèse et Chimie des Mineraux<br />
1a, Rue de la Ferollerie<br />
45045 Orléans Cedex<br />
FRANCE<br />
OKAMURA Makoto<br />
Department of Geology<br />
Faculty of Science<br />
Kochi University<br />
780 Kochi<br />
JAPAN<br />
Tel: (81) 888-44-0111<br />
Fax: (81) 888-43-4220<br />
OLEINIK Larisa M.<br />
Geological Survey “Primorgeologija”<br />
Ocean-prospect, 29/31<br />
690010 Vladivostok<br />
RUSSIA<br />
OLSON Donald L.<br />
Min. Man. Service Arkansas OCS<br />
Region, R.E.<br />
P.O. Box 101159<br />
AK 99510-1159 Anchorage, Arkansas<br />
U.S.A.<br />
ORIGLIA-DEVOS Isabelle<br />
3, Rue Descartes<br />
F-59270 Wasquehal<br />
FRANCE<br />
ORMISTON Allen<br />
AMOCO Production Co.<br />
P.O. Box 3385<br />
OK 74102 Tulsa, Oklahoma<br />
U.S.A.<br />
Tel: (1) 918-6603263<br />
OZVOLDOVA Ladislava<br />
Department of Geology & Paleontology<br />
Faculty of Natural Sciences<br />
J. A. Comenius University<br />
Mlynska Dolina Pav G1<br />
842 12 Bratislava<br />
SLOVAKIA<br />
PAIGE Carrie<br />
Marine Sciences<br />
State University<br />
NY 11794 Stonybrook, New York<br />
U.S.A.<br />
PALMER Amanda<br />
Ocean Drilling Program<br />
Texas AM University<br />
TX 77843 College Station, Texas<br />
U.S.A.<br />
PANASENKO Eugene<br />
Geological Survey “Primorgeologija”<br />
Ocean-prospect, 29/31<br />
690010 Vladivostok<br />
RUSSIA<br />
PAPROTH Eva<br />
Geologisches Landesamt NW<br />
DE-Greii-Str. 195<br />
D-415 Krefeld. GERMANY<br />
Tel: (49) 2151-897296<br />
PARFENOVA T. G.<br />
Tadzhikskaya Univerity<br />
17 Lenin St.<br />
Dunshabe<br />
TADZHIKISTAN<br />
PASZKOWSKI Mariusz<br />
Polish Academy of Sciences<br />
Department of Dinamic Geology<br />
Ul. Senaka 1<br />
31002 Krakow<br />
POLAND<br />
PAYNE Simon<br />
B.P. Petroleum Brittanic House<br />
Moor Lane<br />
Moorgate, London<br />
UNITED KINGDOM<br />
PéREZ-GUZMAN Ana María<br />
Instituto de Geología<br />
Universidad Autónoma de Mexico<br />
(UNAM ) Delegación de Coyoacan<br />
04510 Mexico D.F.<br />
MEXICO<br />
PESSAGNO Emile A.<br />
Program in Geosciences<br />
University of Texas at Dallas<br />
P.O. Box 830688<br />
TX 75083-0688 Richardson, Texas<br />
U.S.A.<br />
Tel: (1) 2146902401<br />
Fax: (1) 2146902537<br />
- 118 -<br />
PETERCAKOVA Maria<br />
Geological Institute<br />
Slovak Academy of Sciences<br />
Dúbravská cesta 9<br />
842 26 Bratislava<br />
SLOVAKIA<br />
PETERSON Susanne<br />
624 National St.<br />
Santa Cruz, California<br />
CA 95060<br />
U.S.A.<br />
PETRUSHEVSKAYA Maria G.<br />
Zoological Institute<br />
Academy of Sciences<br />
University of Nabereshnaya<br />
199054 St. Petersburg<br />
RUSSIA<br />
PISIAS Nicklas G.<br />
College of Oceanography<br />
Oceanograpy Administration. Bld. 104<br />
Oregon State University<br />
OR 97331-5503 Corvallis, Oregon<br />
U.S.A.<br />
E-mail: pisias@oce.orst.edu<br />
POHLER Susanne<br />
Geological Survey of Canada<br />
100 West Pender Street<br />
V6B 1R8 Vancouver, B.C.<br />
CANADA<br />
Tel: (16) 04-6667787<br />
POLUGAR Morton<br />
Chevron Overseas<br />
575 Market Street<br />
CA 94105 San Francisco, California<br />
U.S.A.<br />
POLUZZI A.<br />
Instituto di Geologia<br />
Università di Bologna<br />
Via Zamboni 67<br />
60127 Bologna<br />
ITALY<br />
POPOVA Irina M.<br />
Far Eastern Geological Institute<br />
Russian Academy of Science<br />
159 Prospect, 100 - Letiya<br />
690022 Vladivostok. RUSSIA<br />
Tel: (74) 232-318556<br />
E-mail: fegi@visenet.iasnet.com<br />
PUJANA Ignacio<br />
Laboratorio de Bioestratigrafía<br />
Facultad de Ciencias Naturales<br />
Universidad Nacional de la Patagonia<br />
9000 Comodoro Rivadavia<br />
ARGENTINA<br />
PRALNICOVA I.E.<br />
Geological Institute of the USSR<br />
Academy of Science<br />
Pyshevsky per, 7<br />
Moscow<br />
RUSSIA<br />
RAHMAN S.M. Jubaidur<br />
Geological Survey of Bangladesh<br />
153, Pioneer Road, Segunbagicha<br />
1000 Dhaka<br />
BANGLADESH
Radiolaria 14 Directory<br />
REED Kitty<br />
P.O. Box 5991<br />
WA 98503 Lacey, Washington<br />
U.S.A.<br />
RENZ G. W.<br />
9 Highland Court<br />
CA 94563, Orinda California<br />
U.S.A.<br />
RESHETNYAK V. V.<br />
Zoological Institute<br />
Academy of Sciences<br />
University of Nabereshnaya<br />
199054 St. Petersburg<br />
RUSSIA<br />
REYNOLDS William R.<br />
Department of Geological &<br />
Geophysical Engineering University<br />
of Mississippi<br />
MS 38677 Mississippi<br />
U.S.A.<br />
RIDER Jonathan<br />
101 Broad Street Suite B<br />
CA 95959 Nevada City, California<br />
U.S.A.<br />
RIEDEL William R.<br />
Geological Research Division<br />
Scripps Institution of Oceanography<br />
University of California, San Diego<br />
Ca 92093-0220 La Jolla, California<br />
U.S.A.<br />
Tel: (1) 619-5344386<br />
Fax: (1) 619-5340784<br />
E-mail: wriedel@sdsioa.ucsd.edu<br />
E-mail:71611.1047@compuserve.com<br />
RIEDER Jonathan<br />
6590 E Sargent Rd.<br />
CA 95240 Lodi, California<br />
U.S.A.<br />
RIEGRAF Wofgang<br />
Holandtstr. 55<br />
D-4400 Münster<br />
GERMANY<br />
ROBERTSON A.H.<br />
Department of Geology and Geophysics<br />
University of Edinburgh<br />
Grat Institute, West Mains Road<br />
EH9 3JW Edinburgh<br />
UNITED KINGDOM<br />
Tel: (44) 31-6505943<br />
Fax: (44) 31-6683184<br />
E-mail: ahrobert@glg.ed.ac.uk<br />
ROBERTSON James<br />
Chevron USA<br />
P.O. Box 1660<br />
TX 79702 Midland, Texas<br />
U.S.A.<br />
ROBINSON Brad E.<br />
816 Filmore Dr.<br />
TX 75075 Plano, Texas<br />
U.S.A.<br />
Tel: (1) 214-7546353<br />
ROBSON Simon<br />
Department of Marine Geology Cape<br />
Town University<br />
Rondebosch, Cape Town<br />
SOUTH AFRICA<br />
ROELOFS Adrienne K.<br />
College of Oceanography<br />
Oceanograpy Administration Building<br />
104 Oregon State University<br />
OR 97331-5503 Corvallis, Oregon<br />
U.S.A.<br />
ROMINE Karen<br />
Exxon Production Research<br />
P.O. Box 2189<br />
TX 77001 Houston, Texas<br />
U.S.A.<br />
ROSE Graham<br />
Department of Geological Sciences<br />
University College London<br />
Gower Street<br />
WC1E 6BT London<br />
UNITED KINGDOM<br />
Fax: (44) 71-3887614<br />
ROTH Peter H.<br />
Department of Geology and Geophysics<br />
The University of Utah WBB 717<br />
UT 84112-1138 Salt Lake City, Utah<br />
U.S.A.<br />
ROTHWELL Tom<br />
9 Balasm Ct.<br />
NC 27514 Chapel Hill, North Carolina<br />
U.S.A.<br />
ROWELL H. Chandler<br />
Exxon Co. USA<br />
440 Benmar<br />
TX 77060 Houston, Texas<br />
U.S.A.<br />
RUDENKO Valeriya S.<br />
Far Eastern Geological Institute<br />
Russian Academy of Sciences<br />
159 Prospect, 100 - Letiya<br />
690022 Vladivostok<br />
RUSSIA<br />
RUNEVA N. P.<br />
VNIGNI Micropaleontological<br />
Laboratory<br />
Liteynii propect 39<br />
191104 St. Petersburg<br />
RUSSIA<br />
RYABENSKAYA Irene<br />
Pacific Oceanological Institute Far-<br />
Eatern branch Russian Academy of<br />
Sciences<br />
Baltiyskaya St. 43<br />
690041 Vladivostok<br />
RUSSIA<br />
SACHS H. M.<br />
Department of Geological &<br />
Geophysical Sciences Princenton<br />
University<br />
NJ 08544 Princenton, New Jersey<br />
U.S.A.<br />
SADRISLAMOV B.M.<br />
Uralgeology<br />
Bylvar Davletschinoi, 9<br />
Ufa<br />
RUSSIA<br />
SADUSHI Pellumb<br />
Instituti Geologjik i Naftes e Gazit<br />
Fier<br />
ALBANIA<br />
- 119 -<br />
SAKAI Toyosaburo<br />
Department of Geology<br />
Faculty of General Education<br />
Utsunomiya University<br />
321 Utsunomiya. JAPAN<br />
Tel: (81) 286-36-1515 ext. 602<br />
Fax: (81) 286-36-3171<br />
SANCETTA Constance<br />
Lamont-Doherty Geological<br />
Observatory Columbia university<br />
10964 Palisades, New York<br />
U.S.A.<br />
SANFILIPPO Annika<br />
Geological Research Division<br />
Scripps Institution of Oceanography<br />
University of California, San Diego<br />
Ca 92093-0220 La Jolla, California<br />
U.S.A.<br />
Tel: (1) 619-5342049<br />
Fax: (1) 619-5340784<br />
E-mail: wriedel@odpwcr.ucsd.edu<br />
SANO Hiroyoshi<br />
Dept. of Earth and Planetary Sciences<br />
Kyushu University<br />
812 Fukuoka<br />
JAPAN<br />
SASHIDA Katsuo<br />
Institute of Geoscience<br />
University of Tsukuba<br />
Tennoudai 1-1-1<br />
305 Tsukuba, Ibaraki<br />
JAPAN<br />
Tel: (81) 298-53-4303<br />
Fax: (81) 298-51-9764<br />
SBLENDORIO-LEVY Joanne<br />
Shell Oil Co.<br />
P.O. Box 481<br />
TX 77001 Houston, Texas<br />
U.S.A.<br />
SCHAAF André<br />
Institut de Géologie<br />
1 rue Blessig<br />
F-67084 Strasbourg Cedex<br />
FRANCE<br />
E-mail: aschaaf@illite.u-strasbg.fr<br />
SCHERER Reed. P.<br />
Department of Geological Sciences<br />
Byrd Polar Research Center The Ohio<br />
State University<br />
125 South Oval Mall<br />
OH 43210-1308 Columbus, Ohio<br />
U.S.A.<br />
SCHMIDT-EFFING Reinhardt<br />
Institut für Geologie und Paläontologie<br />
Philipps Universität Lahnberge<br />
Hans Meerwein Strasse<br />
D-3550 Marburg/Lahn<br />
GERMANY<br />
SCHRADER Hans<br />
College of Oceanography<br />
Oceanograpy Administration Building<br />
104 Oregon State University<br />
OR 97331-5503 Corvallis, Oregon<br />
U.S.A.<br />
SCHWARTZAPFEL Jon<br />
22 Bramble Lane<br />
NY 11747 Melville<br />
U.S.A.
Directory Radiolaria 14<br />
SELNICK Martin<br />
Program in Geosciences<br />
University of Texas at Dallas<br />
P.O. Box 830688<br />
75083-0688 Richardson, Texas<br />
U.S.A.<br />
Tel: (1) 214-.6902401<br />
Fax: (1) 214-6902537<br />
SHAKHAWAT HOSSAIN A.T.M.<br />
Department of Geological Sciences<br />
Jahangirnagar University<br />
1342 Savar, Dhaka<br />
BANGLADESH<br />
SHARMA Vijayanand<br />
Department of Geology<br />
University of Delhi<br />
110007 Delhi<br />
INDIA<br />
SHASTINA Valentina V.<br />
Pacific Oceanological Institute<br />
Far-Eatern branch<br />
Russian Academy of Sciences<br />
Baltiyskaya St. 43<br />
690041 Vladivostok<br />
RUSSIA<br />
SHENG Jin-zhang<br />
Laboratory of Palaeobiology and<br />
Stratigraphy Nanjing Institute of<br />
Geology & Paleontology<br />
Academia Sinica<br />
Chi-Ming-Ssu<br />
210008 Nanjing. CHINA<br />
Fax: (86) 25-3357026<br />
SHIKOVA Tanja<br />
Institute of Lithosphera<br />
Academy of Sciences<br />
Staromonethyper, 22<br />
109017 Moscow<br />
RUSSIA<br />
Fax: (70) 95-2335590<br />
SHILOV Valery V.<br />
VNII Okeangeologia<br />
Maklina prosp., 1<br />
190121 St. Petersburg<br />
RUSSIA<br />
SIMES J.E.<br />
Institute of Geological & Nuclear<br />
Science<br />
P.O. Box 30368<br />
Lower Hutt<br />
NEW ZEALAND<br />
SIX Walter M.<br />
Program in Geosciences<br />
University of Texas at Dallas<br />
P.O. Box 830688<br />
75083-0688 Richardson, Texas<br />
U.S.A.<br />
Fax: (1) 214-6902537<br />
SLOAN Jon R.<br />
Geological Department<br />
California State University<br />
CA 91330 Northridge, California<br />
U.S.A.<br />
SMIRNOVA Olga L.<br />
Geological Survey “Primorgeologija”<br />
Ocean prospect, 29/31<br />
690010 Vladivostok<br />
RUSSIA<br />
SMIRNOVA R.F.<br />
Stat of Geological Survey Geological<br />
Department of the Central Ar<br />
2 Toshchinskaya ul. d.10<br />
B-191 Moscow<br />
RUSSIA<br />
SMITH David Thomas<br />
5303 Fleetwood Oaks Dr. 178<br />
TX 75235 Dallas, Texas<br />
U.S.A.<br />
SOEKA Soemoenar<br />
LEMIGAS Indonesia Petroleum<br />
Institute<br />
1089 Jakarta<br />
INDONESIA<br />
SPILLER Frances<br />
Dept. of Geology and Geophysics<br />
University of New England<br />
NSW 2351 Armidale<br />
AUSTRALIA<br />
SPINDLER Michael<br />
Wegener Institute for Polar Research<br />
Columbus Center<br />
D-2850 Bremerhaven<br />
GERMANY<br />
Tel: (49) 471-4831336<br />
SPRAGUE Jamie<br />
Program in Geosciences<br />
University of Texas at Dallas<br />
P.O. Box 830688<br />
75083-0688 Richardson, Texas<br />
U.S.A.<br />
Tel: (1) 2146902401<br />
Fax: (1) 2146902537<br />
STANLEY Edith<br />
604 E 9th Street<br />
CA 95616 Davis, California<br />
U.S.A.<br />
STARRATT Scott W.<br />
U.S. Geological Survey<br />
Paleontological Branch, MS 915<br />
Middlefield Road 345<br />
94025 Menlo Park, California<br />
U.S.A.<br />
Fax: (1) 415-3294975<br />
STASICA Marta<br />
Okolna 22 m 45<br />
30669 Krakow<br />
POLAND<br />
STEIGER Torsten<br />
Institut für Paläontologie<br />
Universität Erlangen-Nürnberg<br />
Loewenichstrasse 28<br />
D-8520 Erlangen<br />
GERMANY<br />
STEINMETZ John<br />
Marathon Oil Co.<br />
P.O. Box 269<br />
CO 80160 Littleton, Colorado<br />
U.S.A.<br />
STEVENS R.K.<br />
Department of Earth Sciences S.J.<br />
Carew Building Memorial<br />
University of Newfoundland<br />
A1B 3X5 St John’s, Newfoundland<br />
CANADA<br />
- 120 -<br />
STINEMEYER Jr. Edwin H.<br />
131 Wetherly Dr<br />
CA 93309 Bakersfield, California<br />
U.S.A.<br />
STRATFORD James<br />
Department of Geology & Geophysics<br />
University of Sydney<br />
NSW 2006 Sydney<br />
AUSTRALIA<br />
STREETER Larisa<br />
P.O. Box 35402<br />
TX 77235-5402 Houston, Texas<br />
U.S.A.<br />
SU Xinghui<br />
Institute of Oceanology<br />
Academia Sinica<br />
7 Nan-Hai Road<br />
3152 Cable-Qingdao<br />
CHINA<br />
Tel: 279062-271<br />
SUGANO Kozo<br />
Division of Natural Science<br />
Osaka kyoiku University<br />
582 Kashivara, Osaka<br />
JAPAN<br />
Tel: (81) 729-76-3211 ext. 4320<br />
Fax: (81) 729-76-3273<br />
SUGIE Hiroyuki<br />
1-9-14 Chuo-higashi<br />
Kuzuu-cho, Aso-gun<br />
327-05 Tochigi<br />
JAPAN<br />
SUGIYAMA Kazuhiro<br />
Department of Earth & Planetary<br />
Sciences Nagoya University<br />
School of Science<br />
464-01 Chikusa, Nagoya<br />
JAPAN<br />
Tel: (81) 052-1893022<br />
SUYARI Kazumi<br />
College of General Education<br />
University of Tokushima<br />
770 Tokushima<br />
JAPAN<br />
SUZUKI Hisashi<br />
Dept. of Geology and Mineralogy<br />
Faculty of Science. Kyoto University<br />
606 Kyoto<br />
JAPAN<br />
SUZUKI Noritoshi<br />
Institute of Geology and Paleontology<br />
Faculty of Science. Tohoku University<br />
980 Aobaku Sendai<br />
JAPAN<br />
SWANBERG Neil R.<br />
Dept.of Fisheries & Marine Biology<br />
University of Bergen<br />
Thormøhlensgt. 55<br />
N-5008 Bergen<br />
NORWAY<br />
E-mail: neil@igbp.kva.se<br />
SZUMAKOW Larisa<br />
Exxon Co. USA<br />
P.O. Box 4279<br />
TX 77001 Houston, Texas<br />
U.S.A.
Radiolaria 14 Directory<br />
TAKAHASHI Kozo<br />
Department of Marine Science<br />
School of Engineering<br />
Hokkaido Tokai University<br />
005 Minami-ku, Sapporo<br />
JAPAN<br />
Tel: (81) 11-571-5112 ext. 615<br />
Fax: (81) 11-571-7879<br />
TAKAHASHI Osamu<br />
Department of Astronomy<br />
and Earth Sciences<br />
Tokyo Gakugei University<br />
4-1-1 Nukui Kita-Machin<br />
184 Koganei, Tokyo<br />
JAPAN<br />
TAKEMURA Atsushi<br />
Geoscience Institute Hygoyo<br />
University of Teacher Education<br />
942-1 Shimokume<br />
673-14 Yashiro-cho, Kato-gun, Hyogo<br />
JAPAN<br />
Tel: (81) 795-44-2206<br />
Fax: (81) 795-44-2189<br />
TAKEMURA Shizuo<br />
Department of Geosciences<br />
Faculty of Sciences<br />
Oska City University<br />
Sugimoto 3-3-138<br />
558 Sumiyoshi, Osaka<br />
JAPAN<br />
Fax: (81) 6-605-2604 or 2522<br />
TAKETANI Yojiro<br />
Fukushima Museum<br />
1-25 Joto-cho, Aizu-Wakamatsu<br />
965 Fukushima<br />
JAPAN<br />
TAN Zhiyuan<br />
Institute of Oceanology<br />
Academia Sinica<br />
7 Nan-Hai Road<br />
3152 Cable-Qingdao<br />
CHINA<br />
Tel: (86) 27-9062271<br />
THEYER Fritz<br />
Hawaii Institute of Geophysics<br />
Room 107<br />
University of Hawaii at Manoa<br />
2525 Correa Road<br />
HI 96822 Honolulu, Hawaii<br />
U.S.A.<br />
THUROW Jürgen<br />
Department of Geological Sciences<br />
University College London<br />
Gower Street<br />
WC1 E6B7 London<br />
UNITED KINGDOM<br />
Fax: (44) 71-3887614<br />
TIKHOMIROVA Ljubov B.<br />
All-Russia Scientific Research<br />
Geological Institute (VSEGEI )<br />
Sredniy Prospect 74<br />
199026 St. Petersburg<br />
RUSSIA<br />
TIPPER Howard<br />
Geological Survey of Canada<br />
100 West Pender Street<br />
V6B 1R8 Vancouver B.C.<br />
CANADA<br />
TOCHILINA Svetlana V.<br />
Pacific Oceanographic Institute<br />
Radfo St<br />
690032 Vladivostok 7<br />
RUSSIA<br />
TOMILSON Andrew J.<br />
Servicio Nacional de Geología<br />
Casilla<br />
14065 Santiago de Chile<br />
CHILE<br />
TONIELLI Renato<br />
Dipartimento de Sienze della Terra<br />
Università “La Sapienza”<br />
P. le A. Moro, 5<br />
00185 Roma<br />
ITALY<br />
E-mail: dottrig@itcaspur<br />
TUMANDA Fe<br />
Mines & Geosciences Bureau<br />
North Avenue<br />
Diliman, Quenzon City<br />
PHILIPPINES<br />
TUMANDA Fe<br />
Institute of Geosciences<br />
University of Tsukuba<br />
Tennoudai 1-1-1<br />
Ibaraki<br />
305 Tsukuba<br />
JAPAN<br />
TUNYOW Huang<br />
Central Geological Survey MOEA<br />
P.O. Box 968<br />
Taipei<br />
TAIWAN R.O.C.<br />
UFFENORDE Henning<br />
Deutsche Texaco AG<br />
Industriestr. 2<br />
D-3109 Wietze<br />
GERMANY<br />
UMEDA Masaki<br />
Department of Geology<br />
Faculty of Science<br />
Shimane University<br />
1060 Nishikawatsu<br />
690 Matsue<br />
JAPAN<br />
Fax: (81) 852-32-6469<br />
URQUHART Elspeth<br />
Department of Geological Sciences<br />
University College London<br />
Gower Street<br />
WC1 E6B7 London<br />
UNITED KINGDOM<br />
Tel: (44) 71-3807131<br />
Fax: (44) 71-3887614<br />
E-mail: ucfbexu@ucl.ac.uk<br />
VAUGHAN Dominique<br />
Elsevier Science Publisher B.V.<br />
Section Geo-Sciences<br />
P.O.Box 1930<br />
1000 BX Amsterdam<br />
THE NETHERLANDS<br />
VENTURINI Maurizio<br />
Instituto di Geologia<br />
Via Zamboni 67<br />
60127 Bologna<br />
ITALY<br />
- 121 -<br />
VISHNEVSKAYA Valentina<br />
Institute of Lithosphera<br />
Academy of Sciences<br />
Staromonethyper, 22<br />
109017 Moscow<br />
RUSSIA<br />
Tel: (70) 95-2307783<br />
Fax: (70) 95-2335590<br />
VITUCHIN D.I.<br />
Geological Institute of the USSR<br />
Academy of Science<br />
Pyshevsky per, 7<br />
Moscow<br />
RUSSIA<br />
VON RAD Ulrich<br />
Bundesanstalt für Geowissenschaften<br />
und Rohstoffe<br />
Postfach 510153<br />
D-3000 Hannover 51<br />
GERMANY<br />
E-mail: vonrad@gate1.bgr.d400.de<br />
WAGNER Dana<br />
Chevron U.S.A. Inc. Western Region<br />
Exploration Department<br />
6001 Bollinger Canyon Road<br />
CA 94583-2398 San Ramon<br />
U.S.A.<br />
Tel: (1) 415-8420428<br />
WAKITA Koji<br />
Department of Geology<br />
Geological Survey of Japan<br />
1-1-3 Higashi<br />
305 Tsukuba, Ibaraki<br />
JAPAN<br />
Fax: (81) 298-543533<br />
WANG Naiwen<br />
Institute of Geology<br />
Academia Sinica<br />
P.O. Box 634 Beijing<br />
CHINA<br />
Tel: 446551-615<br />
WANG Rujian<br />
Department of Marine Geology &<br />
Geophysics Tongji University<br />
1239 Siping Road<br />
200092 Shanghai<br />
CHINA<br />
WANG Yu-jing<br />
Laboratory of Palaeobiology and<br />
Stratigraphy Nanjing<br />
Institute of Geology & Paleontology<br />
Academia Sinica<br />
Chi-Ming-Ssu<br />
210008 Nanjing<br />
CHINA<br />
Fax: (86) 25-3357026<br />
WARNKE Detlef A.<br />
Department of Geological Sciences<br />
California State University<br />
CA 94542 Hayward, California<br />
U.S.A.<br />
WARREN A.D.<br />
Warren Worldwide Inc.<br />
1353 Caminito Faro<br />
CA 92037-7173 La Jolla<br />
U.S.A.
Directory Radiolaria 14<br />
WELLING Leigh A.<br />
College of Oceanography<br />
Oceanograpy Administration Building<br />
104 Oregon State University<br />
OR 97331-5503 Corvallis, Oregon<br />
U.S.A.<br />
E-mail: welling@oce.orst.edu<br />
WHALEN Patricia<br />
Department of Geological Sciences<br />
Southern Methodist University<br />
TX-75275 Dallas, Texas<br />
U.S.A<br />
WHITE Lisa D.<br />
Geology Department<br />
San Francisco State University<br />
1600 Holloway Ave.<br />
CA 94132 San Francisco, California<br />
U.S.A.<br />
WIDZ Daniel<br />
Institute of Geological Sciences<br />
Polish Academy of Sciences<br />
Senacka, 1<br />
31-002 Krakow. POLAND<br />
Tel: (48) 12-221910 or 8929<br />
Fax: (48) 12-222791<br />
WIECZOREK Józef<br />
Polish Geological Society<br />
Historical Geology Section<br />
ul. Oleandry 2a<br />
30063 Kraków<br />
POLAND<br />
WIGLEY Cynthia<br />
Geological Department<br />
Rice University<br />
P.O. Box 1892<br />
TX 77501 Houston, Texas<br />
U.S.A.<br />
WITMER Roger<br />
Union Oil Co.<br />
Sciences & Technology Division<br />
376 S. Valencia Avenue<br />
CA 92621 Brea, California<br />
U.S.A.<br />
WOLFART R.<br />
Federal Geological Survey<br />
Postfach 230153 Stilleweg 2<br />
3 Hannover-Buchholz<br />
GERMANY<br />
WON Hyung Kim<br />
Department of Geology<br />
Stanford University<br />
CA 94305 Stanford, California<br />
U.S.A.<br />
WONDERS Antonius A.H.<br />
British Petroleum Company Ltd. B.P.<br />
Research Centre<br />
Chertsey Road, Sunbury-on-Thames<br />
TW16 7LN Middlesex<br />
UNITED KINGDOM<br />
WRIGHT Anthony J.<br />
Department of Geology<br />
University of Wollongong<br />
P.O. Box 1144<br />
NSW 2500 Wollongong<br />
AUSTRALIA<br />
Tel: (61) 42-270444<br />
Fax: (61) 42-297768<br />
WU Haoruo<br />
Department of Stratigraphy<br />
Institute of Geology<br />
Academia Sinica<br />
P.O. Box 634<br />
100011 Beijing<br />
CHINA<br />
Tel: (86) 44- 6551615<br />
YAGI Nobuyuki<br />
Doctoral Program of Geoscience<br />
University of Tsukuba<br />
Tennoudai 1-1-1<br />
305 Tsukuba, Ibaraki<br />
JAPAN<br />
YAMAGATA Takeshi<br />
Department of Geosciences<br />
College of GeneralEducation<br />
Kyushu University<br />
810 Fukuoka<br />
JAPAN<br />
YAMAMOTO Hirofumi<br />
Department of Marine Geology<br />
Geological Survey<br />
Yatabe<br />
JAPAN<br />
YAMASAKI Tetsuji<br />
Department of Earth<br />
Sciences College of General Education<br />
University of Tokushima<br />
770 Tokushima<br />
JAPAN<br />
YAMASHITA Masayuki<br />
Nishimatsu Co.<br />
2570-4 Shimotsuruma<br />
242 Yamato, Kanagawa<br />
JAPAN<br />
YAMAUCHI Moriyoshi<br />
1-27 Hamadera-Motomachi<br />
592 Sakai, Osaka<br />
JAPAN<br />
YANG Qun<br />
Laboratory of Palaeobiology and<br />
Stratigraphy<br />
Nanjing Institute of Geology &<br />
Paleontology<br />
Academia Sinica<br />
Chi-Ming-Ssu<br />
210008 Nanjing<br />
CHINA<br />
- 122 -<br />
Fax: (86) 25-3357026<br />
YAO Akira<br />
Department of Geoscience<br />
Faculty of Sciences<br />
Osaka City University<br />
Sugimoto 3-3-138<br />
558 Sumiyoshi-ku, Osaka<br />
JAPAN<br />
Tel: (81) 6-605-2604<br />
Fax: (81) 6-605-2604 or 2522<br />
E-mail:<br />
h1682@ocugw.cc.osaka-cu.ac.jp<br />
YEH Hsueh-wen<br />
Hawaii Institute of Geophysics<br />
University of Hawaii at Manoa<br />
2525 Correa Road<br />
HI 96822 Honolulu, Hawaii<br />
U.S.A.<br />
YEH Kuei Yu<br />
National Museum of Natural Science<br />
1 Kuan Chien Rd.<br />
40416 Taichung<br />
TAIWAN R.O.C.<br />
YOSHINO Atsushi<br />
3533-75-107, Kurihara<br />
305 Tsukuba, Ibaraki<br />
JAPAN<br />
YOUNG Jeremy R.<br />
INA Editor<br />
Palaeontology Department<br />
The Natural History Museum<br />
SW7 5BD London<br />
UNITED KINGDOM<br />
E-mail: jy@nhm.ic.ac.uk<br />
ZAGORCEV Ivan<br />
Geological Institute Bulgarian<br />
Academy of Sciences<br />
1113 Sofia<br />
BULGARIA<br />
ZHAMOIDA A.<br />
All-Russia Scientific Research<br />
Geological Institute (VSEGEI )<br />
Sredniy Prospect 74<br />
199026 St. Petersburg<br />
RUSSIA<br />
ZYABREV Sergei V.<br />
Institute of Tectonics & Geophysics<br />
Far East Branch of the Russian<br />
Academy of Sciences<br />
65 Kim Yu Chena Street<br />
680063 Khabarovsk<br />
RUSSIA
Mémoires de Géologie (Lausanne) ISSN 1015-3578<br />
No. 1 BAUD A. 1987. Stratigraphie et sédimentologie des calcaires de Saint-Triphon (Trias, Préalpes, Suisse et France).<br />
202 pp., 53 text-figs., 29 pls. .......................................................................................................................................... $ 20 or CHF 30<br />
No. 2 ESCHER A, MASSON H. and STECK A. 1988. Coupes géologiques des Alpes occidentales suisses. 11 pp., 1 textfigs.,<br />
1 map ............................................................................................................................................................................ $ 20 or CHF 30<br />
No. 3 STUTZ E. 1988. Géologie de la chaîne Nyimaling aux confins du Ladakh et du Rupshu (NW-Himalaya, Inde).<br />
Evolution paléogéographique et tectonique d'un segment de la marge nord-indienne. 149 pp., 42 text-figs., 11 pls. 1<br />
map................................................................................................................................................................................................ 20 or CHF 30<br />
No. 4 COLOMBI A. 1989. Métamorphisme et géochimie des roches mafiques des Alpes ouest-centrales (géoprofil Viège-<br />
Domodossola-Locarno). 216 pp., 147 text-figs., 2 pls. ........................................................................................... $ 20 or CHF 30<br />
No. 5 STECK A., EPARD J.-L., ESCHER A., MARCHANT R., MASSON H. and SPRING L. 1989 Coupe tectonique<br />
horizontale des Alpes centrales. 8 pp., 1 map. ............................................................................................................ $ 20 or CHF 30<br />
No. 6 SARTORI M. 1990. L'unité du Barrhorn (Zone pennique, Valais, Suisse). 140 pp., 56 text-figs., 3 pls. . $ 20 or CHF 30<br />
No. 7 BUSSY F. 1990. Pétrogenèse des enclaves microgrenues associées aux granitoïdes calco-alcalins: exemple des<br />
massifs varisque du Mont-Blanc (Alpes occidentales) et miocène du Monte Capanne (Ile d'Elbe, Italie). 309 pp., 177<br />
text-figs. ................................................................................................................................................................................. $ 20 or CHF 30<br />
No. 8 EPARD J.-L. 1990. La nappe de Morcles au sud-ouest du Mont-Blanc. 165 pp., 59 text-figs. ...................... $ 20 or CHF 30<br />
No. 9 PILLOUD C. 1991 Structures de déformation alpines dans le synclinal de Permo-Carbonifère de Salvan-Dorénaz<br />
(massif des Aiguilles Rouges, Valais). 98 pp., 59 text-figs. ................................................................................... $ 20 or CHF 30<br />
No. 10 BAUD A., THELIN P. and STAMPFLI G. 1991. Paleozoic geodynamic domains and their alpidic evolution in the<br />
Tethys. IGCP Project No. 276. Newsletter No. 2. 155 pp. ....................................................................................... $ 20 or CHF 30<br />
No. 11 CARTER E.S. 1993 Biochronology and Paleontology of uppermost Triassic (Rhaetian) <strong>radiolaria</strong>ns, Queen Charlotte<br />
Islands, British Columbia, Canada. 132 pp., 15 text-figs., 21 pls. ...................................................................... $ 20 or CHF 30<br />
No. 12 GOUFFON Y. 1993. Géologie de la "nappe" du Grand St-Bernard entre la Doire Baltée et la frontière suisse (Vallée<br />
d'Aoste -Italie). 147 pp., 71 text-figs., 2 pls. .............................................................................................................. $ 20 or CHF 30<br />
No. 13 HUNZIKER J.C., DESMONS J., and HURFORD AJ. 1992. Thirty-two years of geochronological work in the Central<br />
and Western Alps: a review on seven maps. 59 pp., 18 text-figs., 7 maps. ........................................................ $ 20 or CHF 30<br />
No. 14 SPRING L. 1993. Structures gondwaniennes et himalayennes dans la zone tibétaine du Haut Lahul-Zanskar oriental<br />
(Himalaya indien). 148 pp., 66 text-figs, 1 map. ....................................................................................................... $ 20 or CHF 30<br />
No. 15 MARCHANT R. 1993. The Underground of the Western Alps. 137 pp., 104 text-figs. .................................. $ 20 or CHF 30<br />
No. 16 VANNAY J.-C. 1993. Géologie des chaînes du Haut-Himalaya et du Pir Panjal au Haut-Lahul (NW-Himalaya, Inde).<br />
Paléogéographie et tectonique. 148 pp., 44 text-figs., 6 pls. ................................................................................. $ 20 or CHF 30<br />
No. 17 PILLEVUIT A. 1993. Les blocs exotiques du Sultanat d'Oman. Evolution paleogeographique d'une marge passive<br />
flexurale. 249 pp., 138 text-figs., 7 pls. ....................................................................................................................... $ 20 or CHF 30<br />
* No. 18 GORICAN S. 1994. Jurassic and Cretaceous <strong>radiolaria</strong>n biostratigraphy and sedimentary evolution of the Budva Zone<br />
(Dinarides, Montenegro). 120 pp., 20 text-figs., 28 pls. ........................................................................................ $ 20 or CHF 30<br />
* No. 19 JUD R. 1994. Biochronology and systematics of Early Cretaceous Radiolaria of the Western Tethys. 147 pp., 29<br />
text-figs., 24 pls. ................................................................................................................................................................. $ 20 or CHF 30<br />
* No. 20 DI MARCO, G. 1994. Les terrains accrétés du sud du Costa Rica. Evolution tectonostratigraphique de la marge<br />
occidentale de la plaque Caraïbe. 166 pp., 89 text-figs., 6 pls. .............................................................................. $ 20 or CHF 30<br />
* No. 21 O'DOGHERTY L. 1994. Biochronology and paleontology of middle Cretaceous <strong>radiolaria</strong>ns from Umbria-Marche<br />
Apennines (Italy) and Betic Cordillera (Spain). 351 pp., 33 text-figs., 73 pls. ................................................ $ 20 or CHF 30<br />
* No. 22 GUEX J. and BAUD A. 1994. Recent Development on Triassic Stratigraphy. 184 pp. ................................... $ 20 or CHF 30<br />
* No. 23 INTERRAD Jurassic-Cretaceous Working Group. 1994. Middle Jurassic to Lower Cretaceous Radiolaria of Tethys:<br />
Occurrences, Systematics, Biochronolgy. 1230 pp., 420 pls. .......................................... please see details inside back-cover<br />
* Volumes 18 to 23 will be available after October 1994<br />
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