radiolaria - Marum
radiolaria - Marum
radiolaria - Marum
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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