23.11.2012 Views

radiolaria - Marum

radiolaria - Marum

radiolaria - Marum

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

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

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!