radiolaria - Marum
radiolaria - Marum
radiolaria - Marum
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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