radiolaria - Marum
radiolaria - Marum
radiolaria - Marum
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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.