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J.M. Berdan

Publications and source records attributed to J.M. Berdan.

8 recordsLinked to original sources
USGS1984

Leperditicopid ostracodes from Ordovician rocks of Kentucky and nearby states and characteristic features of the order Leperditicopida

Leperditicopid ostracodes from the Ordovician formations of Kentucky occur in micritic to fine-grained carbonate rocks believed to represent shallow-water facies. They are found at widely separated horizons in the Middle Ordovician High Bridge Group, the Middle and Upper Ordovician Lexington Limestone, and the Upper Ordovician Ashlock, Bull Fork, and Drakes Formations. In this sequence, the leperditicopes are represented by two genera of leperditiids, Eoleperditia Swartz, 1949 and Bivia Berdan, 1976, and six isochilinid genera, Isochilina Jones, 1858, Teichochilina Swartz, 1949, Ceratoleperditia Harris, 1960, Parabriartina n. gen., Kenodontochilina n. gen., and Saffordellina Bassler and Kellett, 1934; the type species of the hitherto poorly known genus Saffordellina, S. muralis (Ulrich and Bassler, 1923), is redescribed and refigured. In all, 18 taxa, of which 2 are in open nomenclature, are described and illustrated. In addition, the family Isochilinidae Swartz, 1949 is redefined to include genera without marginal brims and with straight ventral contact margins. The morphological characteristics of leperditicopid genera are discussed, and a table listing described genera and their diagnostic features is included.

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USGS1982

Palaeocopid and podocopid Ostracoda from the Lexington Limestone and Clays Ferry Formation (Middle and Upper Ordovician) of central Kentucky

The Middle through lower Upper Ordovician Lexington Limestone and lower part of the Clays Ferry Formation contain an abundant and diversified ostracode fauna. More than 10,000 specimens belonging to 39 genera and 53 species have been found in 73 collections made by members of the U.S. Geological Survey in cooperation with the Kentucky Geological Survey between 1961 and 1970. Five of the genera and 17 of the species are new. New taxa include the genera Gephyropsis, Ningulella, Phelobythocypris, Quasibollia, and Uninodobolba and the following species: Americoncha dubia, Ballardina millersburgia, Brevidorsa strodescreekensis, Ceratopsis asymme , trica C. fimbriata, Ctenobolbina ventrispinifera, Cystomatochilina reticulotiara, Easchmidtella sinuidorsata, Gephyropsis trachyreticulata, Jonesella gonyloba, Laccoprimitia claysferryensis, L. cryptomorphologica, Leperditella? perplexa, Ningulella paupera, Parenthatia sadievillensis, Silenis kentuckyensis, and Uninodobolba franklinensis. In addition, a new species, Quasibollia copelandi, is described from the Middle Ordovician of Ontario. The type specimens of ostracodes previously described from these formations but not represented in the recent collections are redescribed and refigured. The genus Warthinia Spivey, 1939, is reinstated for Ordovician bolliids with two to four nodes, and the genus Ceratopsis Ulrich, 1894, is reviewed with new figures of all known North American species of the genus. Forty-four collections included enough specimens to warrant quantitative analysis. The temporal and spatial distribution of the genera were defined by using Q-mode cluster analysis based on Sorensen's quantified coefficient of association. The resulting phenogram indicated the existence of eight clusters; these clusters were characterized by calculation of constancy and fidelity measures for each of the variables. Generic diversity, compound generic diversity, and lithologic associations were scanned in an attempt to delineate the paleoecologic regime of each cluster. In general, a trend can be seen in which the higher diversity Phelobythocypris-dominated clusters are found in the muddier rocks and less diverse, highly Ceratopsisdominated clusters in the predominantly carbonate members. An exception to this generalization is found in the limestones of the Strodes Creek Member of the Lexington Limestone which has the highest ostracode diversity. However, the Strodes Creek is found entirely within the confines of the muddy Millersburg Member of the Lexington and is believed to represent a similar environment. Diversity differences in these ostracode associations are thought to be controlled mainly by substrate and kinetic energy level. We suggest that the associations may represent ecologically controlled ostracode assemblages.

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