50. PALEOBIOGEOGRAPHIC EVOLUTION OF SHALLOW-WATER ORGANISMS FROM THE APTIAN TO THE EOCENE IN THE WESTERN PACIFIC1

Shallow-water organisms recovered from drilling four guyots in the western Pacific (from the southern Marshall Islands to the Japanese Seamounts) allow the recognition of changes in bioprovinces through time. The Tethyan low-latitude bioprovince characterizes the early Aptian worldwide. In the late Albian, however, shallow-water floral and f aunal assemblages from the drilled guyots, although predominantly composed of cosmopolitan forms, yielded few elements with an areal distribution more restricted to either the Caribbean-central American region or the Mediterranean, suggesting that two bioprovinces had already differentiated at low latitude at that time. During the late Campanian-Maastrichtian, the guyots' area was under the influence of the Caribbean bioprovince, but foraminifer assemblages also include some Mediterranean elements, suggesting that colonization occurred both westward and eastward. In the latest Paleocene-early middle Eocene, the direction of colonization reversed, with prevalent migration from the Mediterranean toward the Pacific.

[1]  J. Masse 1. EARLY CRETACEOUS RUDIST FAUNA OF ALLISON AND RESOLUTION GUYOTS, MID-PACIFIC MOUNTAINS1 , 1995 .

[2]  E. Flügel,et al.  Carbonate platforms as recorders of high‐amplitude eustatic sea‐level fluctuations: the late Albian appenninica‐event , 1993 .

[3]  H. Gillavry,et al.  Review of upper Cretaceous orbitoidal larger foraminifera from Jamaica, West Indies, and their connection with rudist assemblages , 1993 .

[4]  J. Masse The Lower Cretaceous Mesogean benthic ecosystems: palaeoecologic aspects and palaeobiogeographic implications , 1992 .

[5]  J. Butterlin Données nouvelles sur la distribution géographique d'espèces Américaines de Grands Foraminifères du Crétacé Terminal , 1992 .

[6]  E. Barron,et al.  Model Simulation of the Cretaceous Ocean Circulation , 1989, Science.

[7]  K. Konishi Limestone of the Daiichi Kashima Seamount and the fate of a subducting guyot: fact and speculation from the Kaiko “Nautile” dives , 1989 .

[8]  Alfred R. Loeblich,et al.  Foraminiferal Genera and Their Classification , 1988 .

[9]  柴 正博 Geohistory of the Daiichi-Kashima seamount and the Middle Cretaceous eustacy , 1988 .

[10]  P. Skelton The trans-Pacific spread of equatorial shallow-marine benthos in the Cretaceous , 1988, Geological Society, London, Special Publications.

[11]  P. H. Roth Mid-Cretaceous Calcareous Nannoplankton from the Central Pacific: Implications for Paleoceanography , 1981 .

[12]  C. Brusa,et al.  Shallow-Water Skeletal Debris and Larger Foraminifers from Deep Sea Drilling Project Site 462, Nauru Basin, Western Equatorial Pacific , 1981 .

[13]  H. Jenkyns,et al.  Volcanism and vertical tectonics in the Pacific Basin related to global Cretaceous transgressions , 1981 .

[14]  J. Beckmann Shallow-Water Foraminifers and Associated Microfossils from Sites 315, 316, and 318, DSDP Leg 33 , 1976 .

[15]  R. Cowen Faunal provinces in space and time: F. A. Middlemiss, P. F. Rawson and G. Newall (Editors). Geological Journal, Special Issue 4. Seel House PRess, Liverpool, 1971, 236 pp., £5.50 , 1972 .

[16]  M. Glaessner Upper Cretaceous Larger Foraminifera from New Guinea , 1960 .