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 - 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

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

Saved successfully!

Ooh no, something went wrong!