18 resultados para Census and revisitas

em Publishing Network for Geoscientific


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We investigated surface and deep ocean variability in the subpolar North Atlantic from 1000 to 500 thousand years ago (ka) based on two Ocean Drilling Program (ODP) sites, Feni drift site 980 (55°29'N, 14°42'W) and Bjorn drift site 984 (61°25'N, 24°04'W). Benthic foraminiferal stable isotope data, planktic foraminiferal faunas, ice-rafted debris data, and faunally based sea-surface temperature estimates help test the hypothesis that oceanographic changes in the North Atlantic region were associated with the onset of the 100-kyr world during the mid-Pleistocene revolution. Based on percentage of Neogloboquadrina pachyderma (s) records from both sites, surface waters during interglacials and glacials were cooler in the mid-Pleistocene than during marine isotope stages (MIS) 5 and 6. In particular, interglaciations at Bjorn drift site 984 were significantly cooler. Faunal evidence suggests that the interglacial Arctic front shifted from a position between the two sites to a position northwest of Bjorn drift site 984 after ca. 610 ka. As during the late Pleistocene, we find faunal evidence for lagging surface warmth at most of the glacial initiations during the mid-Pleistocene. Each initiation is associated with high benthic d13C values that are maintained into the succeeding glaciation, which we term "lagging NADW production." These findings indicate that lagging warmth and lagging NADW production are robust features of the regional climate system that persist in the middle to late Pleistocene.

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Radiolarian census and abundance data were collected from three deep-sea cores drilled by the Ocean Drilling Program Sites 884, 887 and 1151 to investigate patterns of ecologic changes in space and time during the last 16 million years for the mid-latitude to subarctic North Pacific. High concentrations of radiolarians occurred between 9.0 and 2.7 Ma. Radiolarian species richness was highest in the early middle Miocene at each site and gradually decreased up to about 7 Ma, coinciding with a well-established global cooling trend. A degree of overlap index calculated for radiolarian assemblages revealed 11 faunal change events, of which 8 corresponded to global cooling events and expansions of polar ice sheets. Three of the faunal change events were observed within the peak of radiolarian accumulation rate and were ascribed to changes in primary productivity in the North Pacific rather than global climatic changes. Our assemblage analyses revealed that north-south differentiation in radiolarian assemblages in the northwestern Pacific has existed since 16 Ma and became more distinct via major steps at 6.8 Ma and 2.7 Ma, coinciding with major glaciation events, and that east-west faunal contrasts in the subarctic region became obvious beginning at 11.7 Ma and changed to a different mode around 6.8 Ma. The observed east-west faunal differences possibly reflect east to west climate differences that were characterized by cooler temperatures in the east than the west during the late Miocene (11.7-6.8 Ma) and then by the opposite temperature trend (6.8 Ma-Recent). A severe glaciation at 2.7 Ma played a large role, particularly in temporal changes in radiolarian accumulation rate and assemblage composition.

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Calcareous nannofossils were encountered at only one of the sites (435) drilled during DSDP Leg 56. Cores from Hole 435A yield fairly diverse early and late Pliocene assemblages. The section shows considerable reworking, however. Three to five biostratigraphic datum events provide a reasonable biochronology. The datums range from about 3.3 Ma in Core 11 to about 1.8 Ma in Core 3. Paleobiogeographic data indicate relatively stable and warm climatic conditions in this area in the early Pliocene, becoming more unstable in the late Pliocene when the cosmopolitan species become dominant.

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Analogous to West- and North Africa, East Africa experienced more humid conditions between approximately 12 to 5 kyr BP, relative to today. While timing and extension of wet phases in the North and West are well constrained, this is not the case for the East African Humid Period. Here we present a record of benthic foraminiferal assemblages and sediment elemental compositions of a sediment core from the East African continental slope, in order to provide insight into the regional shallow Indian Ocean paleoceanography and East African climate history of the last 40 kyr. During glacial times, the dominance of a benthic foraminiferal assemblage characterized by Bulimina aculeata, suggests enhanced surface productivity and sustained flux of organic carbon to the sea floor. During Heinrich Stadial 1 (H1), the Nuttallides rugosus Assemblage indicates oligotrophic bottom water conditions and therefore implies a stronger flow of southern-sourced AAIW to the study site. During the East African Humid Period, the Saidovina karreriana Assemblage in combination with sedimentary C/N and Fe/Ca ratios suggest higher river runoff to the Indian Ocean, and hence more humid conditions in East Africa. Between 8.5 and 8.1 kyr, contemporaneous to the globally documented 8.2 kyr Event, a severe reduction in river deposits implies more arid conditions on the continent. Comparison of our marine data with terrestrial studies suggests that additional moisture from the Atlantic Ocean, delivered by an eastward migration of the Congo Air Boundary during that time period, could have contributed to East African rainfall. Since approximately 9 kyr, the gaining influence of the Millettiana millettii Assemblage indicates a redevelopment of the East African fringe reefs.

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The development of models of marine ecosystems in the Southern Ocean is becoming increasingly important as a means of understanding and managing impacts such as exploitation and climate change. Collating data from disparate sources, and understanding biases or uncertainties inherent in those data, are important first steps for improving ecosystem models. This review focuses on seals that breed in ice habitats of the Southern Ocean (i.e. the crabeater seal, Lobodon carcinophaga; Ross seal, Ommatophoca rossii; leopard seal, Hydrurga leptonyx; and Weddell seal, Leptonychotes weddellii). Data on populations (abundance and trends in abundance), distribution and habitat use (movement, key habitat and environmental features) and foraging (diet) are summarised, and potential biases and uncertainties inherent in those data are identified and discussed. Spatial and temporal gaps in knowledge of the populations, habitats and diet of each species are also identified.