radiolaria - Marum
radiolaria - Marum
radiolaria - Marum
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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