23.11.2012 Views

radiolaria - Marum

radiolaria - Marum

radiolaria - Marum

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

Radiolaria 14 Bibliography - 1992<br />

This P. u-forma Group shows a wide variation in its pseudo-abdominal<br />

morphology.<br />

Kuwahara, K. & Sakamoto, M. 1992. Late Permian<br />

Albaillella (Radiolaria) from a bedded chert section in the<br />

Gujo-hachiman area of the Mino Belt, central Japan:<br />

preliminary report on morphometry and cluster analysis. J.<br />

Geosci. Osaka City Univ., 35, 33-52.<br />

Eight species of Late Permian Albaillella (A. excelsa, A. flexa n.<br />

sp., A. Iauta n. sp., A. Ievis, A. sp. aff. A. Ievis, A. triangularis, A. sp.<br />

A, and A. sp. B) were recognized from <strong>radiolaria</strong>n assemblages in a<br />

bedded chert section in the Gujo-hachiman area of the Mino Belt,<br />

Central Japan. Quantitative features were measured for a total of<br />

1000 specimens representing eight species of Albaillella. Their<br />

morphometry indicates morphological distinctions among species.<br />

From their stratigraphic distribution and resemblance of shell forms,<br />

A. excelsa, A. flexa, A. Iauta, A. sp. A, and A. sp. B are considered to<br />

have closely phylogenic relations.<br />

Cluster analysis was attempted to well preserved specimens<br />

representing five species of Albaillella, in order to ascertain<br />

classification by visual inspection. Each clustered group generally<br />

corresponds to each species.<br />

Lazarus, D.B. 1992. Antarctic Neogene <strong>radiolaria</strong>ns from<br />

the Kerguelen Plateau, Legs 119 and 120. In: Proceedings of<br />

the Ocean Drilling Program, Scientific Results. (Wise,<br />

S.W.J., Schlich, R. et al., Eds.), vol. 120. College Station,<br />

TX (Ocean Drilling Program), pp. 785-809.<br />

Abundant, generally well-preserved <strong>radiolaria</strong>ns from Sites<br />

737, 744, 745, 746, 747, 748, and 751 were used in stratigraphic<br />

analysis of Neogene, and particularly middle Miocene to Holocene,<br />

Kerguelen Plateau sediments. The composite Kerguelen section is<br />

more complete than the Weddell Sea sections recovered by Leg 113,<br />

and the <strong>radiolaria</strong>ns are better preserved. Leg 113 <strong>radiolaria</strong>n<br />

zonations of Weddell Sea sites were applicable with only slight<br />

modification, and three new zones—Siphonosphaera vesuvius,<br />

Acrosphaera? Iabrata, and Amphymenium challengerae—are<br />

proposed for the latest Miocene. Geologic age estimates are given<br />

for all <strong>radiolaria</strong>n zones used. Major hiatuses affecting most sites<br />

were seen within the middle Miocene, in the latest Miocene, and<br />

latest Pliocene. Five new species are described: Acrosphaera?<br />

Iabrata, Acrosphaera? mercurius, Siphonosphaera vesuvius,<br />

Actinomma? magnifenestra, and Helotholus? haysi.<br />

Ling, H.Y. 1992. Radiolarians from the Sea of Japan: Leg<br />

128. In: Proceedings of the Ocean Drilling Program,<br />

Scientific Results. (Piscotto, K.A., Ingle, J.C., Von<br />

Breymann, M.T. et al., Eds.), vol. 127-128/1. College<br />

Station, TX (Ocean Drilling Program), pp. 225-236.<br />

The analysis of <strong>radiolaria</strong>ns from Japan Sea subsurface<br />

sediments recovered during Leg 128 of the Ocean Drilling Program<br />

reveals that a warm-water assemblage similar to that of the North<br />

Pacific was replaced by unique post-middle Miocene faunas probably<br />

as a result of the restriction of oceanographic circulation. The<br />

modern fauna was gradually established only in the Pleistocene. No<br />

attempt was made to establish the <strong>radiolaria</strong>n zonation because of<br />

low species diversity and the absence of generally recognized index<br />

forms in the North Pacific. In the diagenetically altered quartz<br />

section, however, a <strong>radiolaria</strong>n assemblage correlative to the middle<br />

Miocene Cyrtocapsella tetrapera Zone of western Honshu was<br />

identified from Hole 799B.<br />

Ling, H.Y. & Kobayashi, H. 1992. Geological<br />

significance of siliceous microfossils from Dogo, Oki<br />

Islands. In: Centenary of Japanese Micropaleontology.<br />

(Ishizaki, K. & Saito, T., Eds.). Terra Scientific Publishing<br />

Company, Tokyo, Japan. pp. 439-447.<br />

Marcucci-Passerini, M. & Gardin, S. 1992. The<br />

Fosso Cupo Formation (northern Latium, Italy): redefinition<br />

and new age data from <strong>radiolaria</strong>n and calcareous nannofossil<br />

biostratigraphy. Cretaceous Res., 13, 549-563.<br />

The "Varicoloured Manganiferous Shales", cropping out at<br />

Monti della Tolfa (northern Latium, Italy) constitute the stratigraphic<br />

substratum of the Upper Cretaceous Pietraforte Flysch in the Ligurid<br />

nappes of the Northern Apennines. These shales are here renamed<br />

the 'Fosso Cupo Formation'. A detailed study of <strong>radiolaria</strong>ns and<br />

calcareous nannofossils permits assignment of this formation to the<br />

Turonian-late Santonian interval. Previous data indicated an<br />

uncertain age ranging from Aptian/Albian to Late Cretaceous. A new<br />

<strong>radiolaria</strong>n subspecies, Crucella cachensis tolfaensis, is described.<br />

- 83 -<br />

Maruyama, T., Takemura, A. & Hiroo, I. 1992.<br />

Result from ODP Leg 120 (Kerguelen Plateau) - Special<br />

reference to diatom, <strong>radiolaria</strong>n and paleomagnetism. Earth<br />

Sci., J. Assoc. geol. Collab. Japan, extra, 6, 154-160. (in<br />

Japanese)<br />

Matsuoka, A. 1992a. Skeletal growth of a spongiose<br />

<strong>radiolaria</strong>n Dictyocoryne truncatum in laboratory culture.<br />

Mar. Micropaleontol., 19/4, 287-297.<br />

The stages of skeletal growth of the <strong>radiolaria</strong>n Dictyocoryne<br />

truncatum were observed using scanning electron and light<br />

microscopy. Four growth stages were recognized through<br />

comparison of laboratory-grown individuals with various sized<br />

skeletons which were collected by plankton tows near Barbados.<br />

Skeletal size is expressed as test height, which is the largest value<br />

among the three dimensions between a base line and arm apex of a<br />

triangular skeleton. The early stage (stage 1), with a maximum<br />

height of less than approximately 120 µm, is a uniformly spongiose,<br />

triangular skeleton lacking arms and a patagium. The next stage<br />

(stage 2) is a triangular skeleton with slightly concave sides of ca.<br />

120-200 µm size with three arms and a lace-like patagium. Further<br />

accretion of silica on the patagium conceals its lace-like structure,<br />

making a skeleton (stage3;ca.200-280 µm) with a more uniformly<br />

spongiose patagium. The mature stage (stage 4) with a maximum<br />

height more than ca. 280 µm is a triangular skeleton with convex<br />

sides, resulting from an outward growth of the patagium. Additional<br />

maturation produces an accretion of spongiose silica on the central<br />

part of the skeleton, forming a thickly biconvex skeleton in<br />

transverse section. One hundred and one individuals of D. truncatum<br />

were cultured in the laboratory at 28 ° C, 35‰ salinity and 165<br />

µE/m 2 /s light intensity, with maximum and mean longevity of 37 and<br />

6.4 days, respectively. The mean growth of 57 specimens which<br />

grew in the laboratory culture was 24.7 µm, with a maximum of 95<br />

µm. The initial size of cultured specimens ranged from 103 to 325<br />

µm, covering all of the four growth stages. Some specimens grew<br />

from one stage to the next stage changing skeletal morphology. The<br />

mean growth rate of four specimens which grew from stage 3 to 4 in<br />

laboratory culture was 5.4 µm/day (range 4.5-6.5 µm/day).<br />

Sporadic growth patterns exhibiting periods of rapid growth (15-20<br />

µm per day ) punctuated by intervals of little or no growth were<br />

observed in some cultured specimens. The sporadic growth may be<br />

related to a physiological rhythm of the organisms rather than<br />

environmental factors. The silica-depositing capacity is related<br />

largely to the vitality of the organisms. Discolored specimens and<br />

specimens with weakly extended axopodia showed no skeletal<br />

growth.<br />

Matsuoka, A. 1992b. Diversity of Jurassic Nassellarians<br />

in Japan. In: Proceedings of the Third Radiolarian<br />

Symposium. (Sakai, T. & Aita, Y., Eds.), vol. 8. News of<br />

Osaka Micropaleontologists, special Volume, Osaka. pp. 63-<br />

66. (in Japanese)<br />

Matsuoka, A. 1992c. Jurassic-Early Cretaceous tectonic<br />

evolution of the Southern Chichibu terrane, southwest Japan.<br />

In: Significance and application of Radiolaria to terrane<br />

analysis. (Aitchison, J.C. & Murchey, B.L., Eds.), vol.<br />

96/1-2. Special Issue: Palaeogeogr. Palaeoclimatol.<br />

Palaeoecol., Elsevier, Amsterdam. pp. 71-88.<br />

The Southern Chichibu terrane fringes the southern margin of<br />

the Jurassic-Early Cretaceous accretionary complex of southwest<br />

Japan. Two subterranes, the Togano subterrane in the north and<br />

Sambosan subterrane to the south, are recognized by examination of<br />

the common features of the terrane. They are juxtaposed throughout<br />

the terrane from western Kyushu to the Kanto Mountains a distance<br />

of over 1000 km. The geology of the Sakawa area, central Shikoku,<br />

is described in detail to show an example of the terrane. The geology<br />

around Tsukumi in eastern Kyushu and Okutama in the Kanto<br />

Mountains is introduced to emphasize the common features of this<br />

terrane.<br />

The Togano subterrane is composed of predominantly Triassic<br />

Jurassic chert clastic sequences associated with subordinate<br />

Jurassic olistostromal sequences and Upper Jurassic-Lower<br />

Cretaceous limestone-bearing clastic sequences. The chert-clastic<br />

sequences show an upward-coarsening sequence which reflects<br />

landward drift of the sea floor from a pelagic realm towards a trench.<br />

The olistostromal sequence contains abundant upper Paleozoic<br />

blocks. This subterrane is characterized by a south-vergent<br />

imbricate structure and south-younging polarity of the chert-clastic<br />

sequences.<br />

The Sambosan subterrane consists of mainly Upper Jurassic-<br />

Lower Cretaceous olistostromal sequences associated with Upper<br />

Jurassic Lower Cretaceous limestone-bearing clastic sequences. The<br />

olistostromal sequence includes abundant Triassic-Jurassic chert<br />

blocks and Triassic limestone blocks accompanied by greenstones.

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

Saved successfully!

Ooh no, something went wrong!