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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.

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