radiolaria - Marum
radiolaria - Marum
radiolaria - Marum
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Bibliography - 1990 Radiolaria 14<br />
preserved Radiolaria were recovered not only from strata overlying<br />
the Josephine ophiolite, but also from within the volcanic member of<br />
the ophiolite. U/Pb geochronometric data constrain the age of the<br />
Mirifusus first-occurrence event to after 162 ± 1 Ma and to being<br />
157 ±1.5 Ma or slightly older. Radiolarian faunal data indicate that<br />
the Josephine ophiolite originated at Central Tethyan paleolatitudes<br />
during the latest Callovian (162 Ma) and was carried northward to<br />
Northern Tethyan and Southern Boreal paleolatitudes during the<br />
Oxfordian.<br />
Petercáková, M. 1990. Radiolarian from cherts of the<br />
Kalisco limestone formation of the Manin unit (Butkov,<br />
West Carpathians). Geol. Sb. (Bratislava), 41/2, 155-169.<br />
The work deals with the first occurrence of <strong>radiolaria</strong>ns in the<br />
Lower Cretaceous pelagic sediments of the Manin unit of the West<br />
Carpathians. The <strong>radiolaria</strong>ns come from cherts of Kalisco<br />
Limestones that in the past were stratigraphically investigated by<br />
means of ammonites and tintinnoid organisms (Vasicek—Michalik,<br />
1986; Borza et al., 1987). Radiolarian species characterizing the<br />
zone Mirifusus chenodes (sensu SCHAAF, 1984) were identified,<br />
which stratigraphically corresponds to the uppermost part of the<br />
Lower Hauterivian.<br />
Petrushevskaya, M.G. & Swanberg, N.R. 1990.<br />
Variability in skeletal morphology of colonial Radiolaria<br />
(Actinopoda: Polycystinea: Collosphaeridae).<br />
MIcropaleontoloy, 36/1, 65-85.<br />
Skeletal morphology is used to determine species in almost all<br />
Radiolaria, and in many cases relatively fine differences between<br />
morphotypes are used to distinguish between species. While many<br />
Radiolaria have been described from very few specimens we have<br />
little knowledge of variability of Radiolaria because we have been<br />
able to study few known biological populations of a species. This<br />
problem has been addressed by examining the variation occurring<br />
within colonies of collosphaerid Radiolaria, and comparing it to that<br />
occurring between colonies of the same and other species. As far as<br />
we know the cells within such colonies are genetically identical and<br />
therefore intra-colony variation must be caused by other than<br />
species-level phenomena.<br />
Both quantitative and qualitative features were considered in a<br />
detailed study of a total of 2922 skeletons in 44 colonies<br />
representing 12 species. The results of this analysis have revealed<br />
substantial variation in both quantitative and qualitative features,<br />
both between and within colonies of a species. Furthermore, typically<br />
1-5% and sometimes even 10-20% of the individuals in a colony<br />
possess some structures which are absent in the majority of<br />
individuals of the species. The structures which are characteristic<br />
for one species, typically occurred at a low rate in another. No<br />
smooth transition between species was seen provided that one<br />
considered the whole suite of diagnostic morphological features and<br />
not just a single character. Caution is strongly urged in uncertain<br />
species assignments and it is asserted that it is absolutely<br />
impossible to erect new species on the basis of a few specimens<br />
which are non-identical, or on the appearance of a single feature.<br />
Raymond, D. & Lethiers, F. 1990. Signification<br />
géodynamique de l'événement radiolaritique dinantien dans les<br />
zones externes sud-varisques (Sud de la France et Nord de<br />
l'Espagne). C.R. Acad. Sci. (Paris), Sér. II, 310, 1263-1269.<br />
In the South of France and the North of Spain the radiolarites<br />
from Dinantian age have been deposited in a narrow basin initiated<br />
since the Frasnian times and bordered by emerged areas. The<br />
starting of the siliceous deposition would be related to the<br />
installation of cold deep-water currents coming from a Late<br />
Devonian-Early Carboniferous glacial North-Gondwanian area.<br />
Special ostracod faunas corroborate these paleoecologic changes.<br />
Renz, G.W. 1990. Ordovician Radiolaria from Nevada and<br />
Newfoundland a comparison at the family level. Mar.<br />
Micropaleontol., 15/3-4, 393-402.<br />
Two Ordovician <strong>radiolaria</strong>n assemblages from North America<br />
are examined and compared at the family (group) level. In the<br />
material from Newfoundland (Middle Ordovician—Llanvirnian, after<br />
Bergstrom, 1974), well-preserved specimens are common, 92%<br />
being spherical polycystines. In the Nevada material (Upper<br />
Ordovician—Caradocian, after Dunham and Murphy, 1976), wellpreserved<br />
specimens are abundant and coated with iron oxide. Here<br />
species of spherical polycystines constitute only 42% of the<br />
population while species of Palaeoscenidiidae, after their appearance<br />
and radiation within the preceding 25 million years, constitute 47%.<br />
Results of this comparison at the family level suggest that for<br />
<strong>radiolaria</strong>ns, evolutionary change during the Ordovician was not slow<br />
- 54 -<br />
as previously thought. Rather, this was a time of growth, radiation<br />
and experimentation.<br />
Riedel, W.R. 1990. Quantitative description of pore<br />
patterns in <strong>radiolaria</strong>. Micropaleontology, 36/2, 177-181.<br />
The arrangement of pores in the lattice-shells of <strong>radiolaria</strong>ns<br />
can be an important descriptor of the skeletons, if the pattern can<br />
be characterized quantitatively. An image analysis system<br />
integrated with a personal computer provides a convenient means of<br />
measuring distances between pores, and their angular relations,<br />
together with the variability of those measures. Both regular and<br />
irregular patterns can be quantified. The procedure is adaptable to a<br />
wide spectrum of patterns in the organic world.<br />
Sanfilippo, A. 1990. Origin of the subgenra<br />
Cyclampterium, Paralampterium and Sciadiopeplus from<br />
Lophocyrtis (Lophocyrtis) (Radiolaria, Theoperidae). Mar.<br />
Micropaleontol., 15/3-4, 287-312.<br />
Work on the exceptionally well-preserved, rapidly accumulating<br />
Bath Cliff Section, Barbados and supplementary Deep Sea Drilling<br />
Project samples, has revealed the evolutionary origins of three<br />
stratigraphically useful species in the Cryptoprora ornata Zone<br />
straddling the Eocene/Oligocene boundary and demonstrated the<br />
origin of the genus Cyclampterium. Elucidation of the origin of<br />
Cyclampterium milowi necessitates a revision of the genera<br />
Lophocyrtis and Cyclampterium. Lophocyrtis (Lophocyrtis) jacchia is<br />
the ancestor of L. (Cyclampterium) hadra, the earliest member in the<br />
subgenus Cyclampterium which comprises the anagenetic lineage<br />
leading from L. (C.) hadra to L. (C.) neatum. The monotypic subgenus<br />
Sciadiopeplus branches off from an early member in the<br />
Cyclampterium lineage. The new species L. (L.) exitelus and L. (S.)<br />
oberhaensliae terminate the subgenera Lophocyrtis and<br />
Sciadiopeplus, respectively. During the investigation it also became<br />
clear that morphotypes resembling early L. (C.) milowi could be<br />
found in mid and high latitude assemblages in the late Early and late<br />
Middle Eocene. The origin of one these morphotypes was also traced<br />
to L . (Lophocyrtis) jacchia giving rise to the new subgenus<br />
Paralampterium. This lineage includes the new species L .<br />
(Paralampterium) dumitricai and two species questionably assigned<br />
to it, L. (Paralampterium) ? Iongiventer and the new species L.<br />
(Paralampterium) ? galenum. The relationship of L. (P.) dumitricai to<br />
L. (P.) ? Iongiventer and L. (P.) ? galenum is unknown.<br />
Schwartzapfel, J.A. 1990. Biostratigraphic<br />
investigations of Late Paleozoic (Upper Devonian to<br />
Mississipian) Radiolaria within the Arbuckle Mountains and<br />
Ardmore. Ph.D Thesis. Programs in Geoscience, University<br />
of Texas at Dallas, p. (unpublished)<br />
Sedlock, R.L. & Isozaki, Y. 1990. Lithology and<br />
biostratigraphy of Franciscan-like chert and associated rocks<br />
in west-central Baja California, Mexico. Geol. Soc. Amer.,<br />
Bull., 102, 852-864.<br />
We present the result of biostratigraphic and lithologic studies<br />
of ribbon chert and associated rocks in a Mesozoic subduction<br />
complex in west-central Baja California, Mexico. The subduction<br />
complex terrane is divided into three subterranes, each of which<br />
consists of an originally coherent sequence of interbedded oceanic<br />
rocks, including ocean-floor basalt, terrigenous siliciclastic<br />
turbidites, <strong>radiolaria</strong>n ribbon chert, and limestone. Parts of the<br />
original stratigraphy are preserved in the least deformed, least<br />
metamorphosed subterrane. Ocean-floor pillow basalt on Cedros<br />
Island is overlain by about 40 m of <strong>radiolaria</strong>n ribbon chert ranging in<br />
age from Early Jurassic or older to Early Cretaceous; the chert is<br />
overlain by thin-bedded turbidites. On San Benito West Island,<br />
<strong>radiolaria</strong>n ribbon chert is interbedded with volcanogenic rocks,<br />
including a megabreccia that contains blocks of metabasites, folded<br />
Late Jurassic-Early Cretaceous chert, and marble in a mid-<br />
Cretaceous radiolarite matrix. Chert samples from tectonically<br />
thinned sequences elsewhere on Cedros and San Benito Islands<br />
contain Late Triassic to Early Cretaceous <strong>radiolaria</strong>n assemblages.<br />
The 40-m-thick chert section on Cedros Island probably<br />
accumulated atop oceanic crust in a large ocean basin for at least<br />
65 m.y. and was later capped by terrigenous turbidites as it<br />
approached the subduction zone along the western margin of North<br />
America. Faulted chert sections on Cedros and San Benito Central<br />
and West Islands are subsets of the main section on Cedros Island.<br />
The chert/megabreccia section on San Benito West Island is<br />
interpreted to have accumulated at the foot of a volcanic edifice on<br />
the ocean floor (for example, seamount, fracture zone) or during<br />
extension and normal faulting of the downgoing oceanic plate in a<br />
subduction zone. Sedimentary structures and stratigraphic relations<br />
indicate that all ribbon chert in this subduction complex was<br />
deposited by sediment gravity flows; that is, they are turbidites.