367 resultados para 105-647B


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Faunal and stable isotopic data in Sites 646 and 647 provide a ~0.9-Ma paleoclimatic and paleoceanographic record for the Labrador Sea, that is supported by a floral record for the past ~0.3 Ma. At both sites, most glacial stages generally are dominated by polar fauna and flora with low species diversity. Although minor occurrences of subpolar species also were observed in lowermost parts of several glacial stages in Site 646, the faunal classification of Ruddiman and Mclntyre (1976) suggested the presence of polar ecological water masses in the area during most of the glacial periods. In several glacial stages at Site 647, both the faunal and floral data indicate that early periods were marked by subpolar and transitional ecological water masses. The interglacials are characterized by a polar fauna at Site 646 and by polar and transitional faunas and floras at Site 647. However, several interglacial stages in Site 646 include a subpolar flora, in contrast to a planktonic foraminifer fauna similar to that found in the glacial stages. The occurrence of subpolar water masses in several glacial isotopic stages indicates significant northward advection of warmer waters into the Labrador Sea during the early glacial periods, which provided a corridor of oceanic warmth extending from mid- to high latitudes and contributed an additional source of moisture for continental ice-sheet growth. Similar conditions also were documented in the northwest Labrador Sea, Grand Banks, and the North Atlantic.

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Possible genetic relationships between syn- and post-depositional processes and sediment microstructure were investigated. Samples from cores at Sites 646 and 647 of Ocean Drilling Program (ODP) Leg 105 included examples of bottom current deposition (contourites), turbidity current deposition, consolidation, and diagenesis. Examination of nearly 200 micrographs of 14 samples from Site 646 and 13 samples from Site 647 leads to the conclusion that sedimentation processes do not appear to have an obvious influence on fabric. The effects of post-depositional processes, such as bioturbation, coring disturbance, and even remolding, appear to be less significant than one might expect as a result of the relatively coarse grain size of the sediments studied. Consolidation resulting from increased overburden stress results in increased particle alignment and compression of fabric elements with depth. The transition from open, random fabric in shallow samples to preferred orientation at depth represents the only change in these sediments that can be ascribed directly to a specific depositional or post-depositional process. Mineralogical variations, owing to changes in weathering processes and growth of authigenic/diagenetic minerals, also have a pronounced effect on sediment fabric.

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The quantity and quality of organic carbon of Eocene to Holocene sediments from ODP Sites 645, 646, and 647 were investigated to reconstruct depositional environments. Results were based on organic-carbon and nitrogen determinations, Rock-Eval pyrolysis, and kerogen microscopy. The sediments at Site 645 in Baffin Bay are characterized by relatively high organic-carbon values, most of which range from 0.5% to almost 3%, with maximum values in the middle Miocene. Distinct maxima of organic-carbon accumulation rates occur between 18 and 12.5 Ma and between 3.4 and 0 Ma. At Sites 646 and 647 in the Labrador Sea, organic-carbon contents vary between 0.1% and 0.75%. Cyclic 'Milankovitch-type' changes in organic-carbon deposition imply climate-controlled mechanisms that cause these fluctuations. The composition of organic matter at Site 645 is dominated by terrigenous components throughout the entire sediment sequence. An increased content of marine organic carbon was recorded only in the late-middle Miocene. At Sites 646 and 647, the origin of the organic matter most probably is marine. Oceanic paleoproductivity values were estimated, based on the amount of marine organic carbon. During most of the Neogene time interval at Site 645, productivity was low, i.e., similar or less than that measured in Baffin Bay today. Higher values of up to 150 (200) gC/m**2/y may have occurred only in the Miocene. At Sites 646 and 647, mean paleoproductivity values vary between 90 and 170 gC/m**2/y; i.e., these are also similar to those measured in the Labrador Sea today. Lower values of 40 to 70 gC/m**2/y were estimated for the early Eocene and (middle) Miocene.

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Basalt samples recovered from the lowermost 37 m of Leg 105 Hole 647A in the Labrador Sea are fine- to medium grained, have microphenocrysts of clinopyroxene, and show little evidence of alteration. Chemically, these rocks are low potassium (0.01-0.09 wt% K20), olivine- to quartz-normative tholeiites that are also depleted in other incompatible elements. In terms of many of the incompatible trace elements, the Labrador Sea samples are similar both to iV-type midocean ridge basalts (MORBs) and to the terrestrial Paleocene volcanic rocks in the Davis Strait region of Baffin Island and West Greenland. However, significant differences are found in their strontium and neodymium isotope systematics. Hole 647A samples are more depleted in epsilon-Nd (+9.3) and are anomalously rich in 87Sr/86Sr (0.7040) relative to the Davis Strait basalts (epsilon-Nd +2.54 to + 8.97; mean 87Sr/86Sr, 0.7034). We conclude that the Hole 647A and Davis Strait basalts may have been derived from a similar depleted mantle source composition. In addition, the Davis Strait magmas were generated from mantle of more than one composition. We also suggest that there is no geochemical evidence from the Hole 647A samples to support or to refute the existence of foundered continental crust in the Labrador Sea.

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In this preliminary biometric study of the calcareous nannofossil species Chiasmolithus expansus, Chiasmolithus oamaruensis, and Chiasmolithus altus from the upper middle Eocene to lower Oligocene of Sites 647 and 748, we document a complete gradation of forms among all three species. Chiasmolithus oamaruensis has significantly higher morphologic variance than the other species. The Chiasmolithus population at each site changes from C. expansus to C. oamaruensis and then to C. altus. This may not reflect a true evolutionary sequence because a major reversal in shape change of the central cross-bar structure accompanies this sequence, and because C. altus is morphologically closer to C. expansus than it is to C. oamaruensis. The change in the width of the cross-bar structure is primarily a result of changes in the alignment of the central connecting bar, rather than of changes in the cross-bar angle. At Site 748, two fluctuations in morphology produce sample populations intermediate between all three species. In addition, reported stratigraphic and paleogeographic occurrences of C. oamaruensis and C. altus show different latitudinal distributions. These morphological and distributional patterns may be explained by a continuous morphologic gradient between C. oamaruensis and C. altus, with C. oamaruensis occurring more commonly in cool-water paleoenvironments, and C. altus occurring more commonly in cold-water paleoenvironments. Thus, paleoenvironmental fluctuations at Site 748 may be the cause of the morphologic fluctuations in Chiasmolithus. This hypothesis can be tested against previously proposed evolutionary models by more detailed sampling of sections along a latitudinal transect.