USGS · 70030034
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J.K. Rigby, K.J. Cunningham. 2007. A new, large, late pleistocene demosponge from Southeastern Florida. https://doi.org/10.1666/pleo0022-3360(2007)081%5B0788%3Aanllpd%5D2.0.co%3B2
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Three types of geographic isolation—land barriers, deep water barriers, and climatic barriers—resulted in three distinct evolutionary responses in Neogene and Quaternary species of the epineritic ostracode genus Puriana . Through systematic, paleobiogeographic, and morphologic study of several hundred fossil and Recent populations from the eastern Pacific, western Atlantic, Gulf of Mexico, and the Caribbean, the phylogeny of the genus and the geography of speciation events were determined. Isolation of large populations by the Isthmus of Panama during the Pliocene did not lead to lineage splitting in species known to have existed before the Isthmus formed. Conversely, the establishment of small isolated populations on Caribbean islands by passive dispersal mechanisms frequently led to the evolution of new species or subspecies. Climatic changes along the southeastern United States during the Pliocene also catalyzed possible parapatric speciation as populations that immigrated to the northeastern periphery of the genus' range split to form new species. The results provide evidence that evolutionary models describing the influence of abiotic events on patterns of evolution and speciation can be tested using properly selected tectonic and climatic events and fossil groups amenable to species-level analysis. Two new species, P. bajaensis and P. paikensis , are described.
Cretaceous clavagellid pelecypods are a poorly known group, and have previously received little study. Ascaulocardium armatum is conchologically the most complex burrowing pelecypod known. From the study of living clavagellids, it is possible to interpret the various tubes extending outward from the adventitious crypt of A. armatum as devices for hydraulic burrowing and deposit feeding. The conchologically complex A. armatum occurs near the beginning of the history of the Clavagellidae, and does not seem to have given rise to any younger species. Ascaulocardium armatum is known only from the Upper Cretaceous rocks (Santonian–Maastrichtian) of the east Gulf and Atlantic Coastal Plains of the United States of America, as is probably the genus Ascaulocardium . All known Cretaceous clavagellids are burrowing species having a free right valve, and this is the ancestral mode of life of the Clavagellidae. Clavagellids that have a boring habit are a more recent evolutionary development, as are burrowing species having both juvenile valves cemented to the crypt. Clavagellids probably evolved from Jurassic–Early Cretaceous pholadomyids. Almost all Cretaceous clavagellids occur outside the Tethyan Zoogeographic Realm; this distribution is in marked contrast to the modern distribution of the family. Living species mostly inhabit clear, shallow seas in subtropical to tropical shelf areas.
Upper Cretaceous rocks of the Kuskokwim Group are exposed in a large region of southwestern Alaska and are mainly composed of deformed turbidite deposits that contain few fossils other than inoceramid bivalves. This paper documents the taxonomy of the inoceramids in the Kuskokwim Group, develops an inoceramid biostratigraphy based on known ranges in other regions, and analyzes biogeographic patterns, paleoecology, and depositional history of the Kuskokwim Group. Most of the inoceramid bivalves present in the Kuskokwim Group are of Cenomanian and Turonian age, and an assemblage of species typical of late Turonian age rocks is particularly well developed. Only two localities appear to be as young as Santonian age. The following 16 species or subspecies are discussed and illustrated in detail: Birostrina tamurai Matsumoto and Noda, Inoceramus virgatus Schlüter, I. pennatulus Pergament, I. pictus minus Matsumoto, I. cf. I. yabei Nagao and Matsumoto, I. ? sp. aff. I. costatus Nagao and Matsumoto, I. hobetsensis Nagao and Matsumoto, I. longealatus Tröger, I. frechi Flegel, I. waltersdorfensis waltersdorfensis Andert, I. cf. I. waltersdorfensis hannovrensis Heinz, I. kuskokwimensis n. sp., Mytiloides cf. M. opalensis (Böse), M. teraokai (Matsumoto and Noda), M. cf. M. incertus (Jimbo), and Sphenoceramus naumanni (Yokoyama). In addition, a specimen with affinities to Mytiloides striatoconcentricus carpathicus (Simionescu) and a specimen that may belong to the I. (Cremnoceramus?) rotundatus–I. ( C .) erectus lineage are illustrated. Most of the taxa present in the Kuskokwim region are found in other regions of the North Pacific, particularly Japan and eastern Siberia, or are found throughout the Northern Hemisphere. Only one species, I. kuskokwimensis n. sp., is new and may be endemic. North Pacific taxa are predominant in the Kuskokwim region, but intervals near the Cenomanian–Turonian Stage boundary and in the upper Turonian contain taxa characteristic of Europe and the Western Interior basin of North America; some of these taxa have not been recorded previously in the North Pacific region. Turonian heteromorph ammonite assemblages associated with inoceramids in the finer grained facies of the Kuskokwim region are similar to those found in coeval rocks of Japan and Germany. The depositional area of the Kuskokwim Group can be broken into two northeast-trending subbasins, the Kuskokwim River subbasin to the northwest and the Mulchatna River subbasin to the southeast, connected by the Nushagak Hills corridor. Within the Kuskokwim River subbasin, deposition apparently started earlier in the north (middle Cenomanian) than in the south (late Cenomanian to early Turonian), and prograding deltaic sedimentation along the western margin also appears to have started earlier in the north. No marine fossils younger than latest Turonian to earliest Coniacian are known from the Kuskokwim River subbasin. The youngest fossils identified are Santonian in age and are from deep-water deposits in the Nushagak Hills corridor. Few fossils are known from the Mulchatna River subbasin and age control is limited.