574 resultados para 108-667


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High-resolution records (2 7 kyr) of Upper Pliocene Discoaster abundances obtained from six ODP/DSDP sites are assessed independently using oxygen isotope stratigraphy. Four Atlantic Ocean sites (DSDP Sites 552 and 607, and ODP Sites 659 and 662) comprise a transect from 56°N to 1°S and provide a record of latitudinal variations in Diseoaster biogeography. Low-latitude sites in the Atlantic (ODP Site 662), Pacific (ODP Site 677), and Indian (ODP Site 709) oceans provide additional information about variability in Discoaster abundance patterns within the equatorial region. A common chronology, based on the astronomical time scale developed for ODP Site 677, has been established for all the sites. By integrating oxygen isotope data and Discoaster abundance records at each site we are able to independently evaluate the temporal and spatial distribution of D. brouweri and D. triradiatus in the 500 kyr prior to the extinction of the discoasters near the base of the Olduvai subchron. Major decreases in abundance are evident during some of the more intense late Pliocene glacial events. In particular, glacial isotope stages 82, 96, 98 and 100 are associated with distinct abundance minima. At these times, large-scale changes in surface hydrographic conditions appear to have suppressed Discoaster numbers on a global scale. The increase in abundance of D. triradiatus, which precedes the extinction of the discoasters by around 200 kyr, may also be related to the intensification of environmental pressures that accompanied the build-up of Northern Hemisphere ice sheets during the late Pliocene. In spite of contrasting geographic and oceanographic settings, the various D. brouweri and D. triradiatus records are remarkably similar. This demonstrates that the acme and extinction events are excellent biostratigraphic datums. The simultaneous extinction of D. brouweri and D. triradiatus at 1.95 Ma were synchronous events at both a regional scale within the Atlantic, and on a global scale between the three major oceans. However, the start of the D. triradiatus acme appears to have been diachronous, occurring some 40 kyr earlier in the Atlantic than in the Indo-Pacific, and hence the stratigraphic usefulness of this datum is regional rather than global.

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We have integrated Oligocene to lower upper Miocene planktonic foraminifer biostratigraphy with benthic foraminifer (Cibicidoides spp.) stable isotope records for two sites drilled on opposite sides of the Sierra Leone Rise in the eastern equatorial Atlantic Ocean. Deep Sea Drilling Project Site 366 (2853 m present water depth; 2200-2800 m paleodepth) recovered an Oligocene to upper Miocene record with a minor unconformity in the "middle" Oligocene and a condensed middle Miocene section. Ocean Drilling Program Site 667 (3529 m present depth; 3000-3500 m paleodepth) recovered an apparently continuous "middle" Oligocene to lower middle Miocene record and a similar condensed middle Miocene section. The Oligocene to lower Miocene sections were deposited at similar sedimentation rates (~11-16 m/m.y.). Stable isotope stratigraphy proved to be useful in establishing intra- and interbasinal correlations. In addition to the well-known earliest Oligocene and middle Miocene S180 increases, a distinct d18O increase occurred near the Oligocene/Miocene boundary. Carbon isotope variations provide similar potential for improving correlations; for example, a d13C increase occurred near the Oligocene/Miocene boundary in concert with increased d18O values. There was little d13C difference between the western Atlantic and eastern Atlantic basins during the late Oligocene and most of the middle Miocene; in contrast, eastern basin d13C values were slightly lower than those in the western basins during the earliest Oligocene (about 35-33 Ma) and early Miocene (about 22-18 Ma).

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Detailed quantitative analyses of selected calcareous nannofossil species were used to determine the placement of zonal boundaries. In Hole 667A in the equatorial Atlantic Ocean, Zones CP19 through CN5 were recognized, whereas at Site 574 in the equatorial Pacific Ocean, only the CN4/CN5 boundary could be determined. Boundaries were identified by sharp rises and declines in abundance at the beginnings and ends, respectively, of index fossil ranges. The sharp rise in abundance at the beginning of the range of Triquetrorhabdulus rugosus provided a good datum level in both regions; the same is true for the sharp decline in abundance at the end of the range of Cyclicargolithus floridanus. The last occurrence of Helicosphaera ampliaperta was used to mark the CN3/CN4 boundary in Hole 667A, while at Site 574, H. ampliaperta was absent. The abundance pattern of Triquetrorhabdulus carinatus obtained from Hole 667A makes it impossible to observe a distinct disappearance level. Age/depth plots reveal uniform sedimentation rates at both sites during early Miocene times. At Site 667 in the Atlantic the mean sedimentation rate was 14.90 m/m.y., and at Site 574 in the Pacific it was 16.17 m/m.y. during this same period. One new nannofossil species, Triquetrorhabdulus rioensis, is described; and one species, Triquetrorhabdulus serratus, is recombined.

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