994 resultados para Sr isotope
Resumo:
Identifying terrigenous sources in deep-sea sediments may reveal temporal trends in paleocirculation and the relative role of eolian, upwelled, and hemipelagic Fe sources to surface waters. Bulk elemental and isotopic geochemistry of deep-sea sediments recovered during Ocean Drilling Program Leg 177 in the southeastern Atlantic sector of the Southern Ocean reveal several important aspects of paleocirculation and terrigenous provenance. The sites studied span 43°-53°S and represent different oceanographic settings relative to regional hydrography and sediment type. Bulk sediment geochemistry indicates that terrigenous provenance varied over the past 600 k.y. Site 1089, the northernmost site, exhibits clear glacial-interglacial variability in provenance, while provenance appears to vary regardless of climate state at the more southerly sites (Site 1093 and 1094). Nd and Sr isotopes and Sm/Nd ratios of the terrigenous fraction indicate that study sites have geochemically distinguishable provenance. Nd and Sr isotopes further suggest that Sites 1089 and 1094 both contain detrital components that originated in South America over the past 30 k.y.; however, Site 1089 is also influenced by southern African sources and the strength of the Agulhas Current. The e-Nd data support a more hemipelagic source for the terrigenous material rather than an eolian source based on comparisons with Antarctic ice core data and known sea-ice extent.
Resumo:
A detailed Pliocene oxygen isotope record from the Ontong Java Plateau, based on measurements of the surface-dwelling planktonic foraminifer Globigerinoides sacculifer, was produced for the period from 5 to 2 Ma. The record documents major long- and short-term climate changes. The results show periods of enhanced ice volume at 4.6 to 4.3 Ma and after 2.85 Ma, a long-term warming trend from 4.1 to 3.7 Ma, and a distinct cooling trend that was initiated at 3.5 Ma and progressed through the initiation of large-scale Northern Hemisphere glaciation after 2.85 Ma (according to the time scale of Shackleton and others proposed in 1990). Periods of high average ice volumes also show the highest d18O amplitudes. The pattern of climate cyclicity changed markedly at about 2.85 Ma. Earlier times were marked by high-frequency variability at the precessional frequencies or even higher frequencies, pointing to low-latitude processes as a main controlling factor driving planktonic d18O variability in this period. The high-frequency variability is not coherent with insolation and points to strong nonlinearity in the way the climate system responded to orbital forcing before the onset of large scale Northern Hemisphere glaciation. After 3 Ma, stronger 41-k.y. cyclicity appears in the record. The shift in pattern is clearest around 2.85 Ma (according to the time scale proposed by Shackleton and others in 1990), 100-200 k.y. before the most dramatic spread of Northern Hemisphere ice sheets. This indicates that high-latitude processes from this point on began to take over and influence most strongly the d18O record, which now reflects ice-volume fluctuations related to the climatic effects of obliquity forcing on the seasonality of high-latitude areas, most probably in the Northern Hemisphere. The general Pliocene trend is that high-latitude climate sensitivity and instability was increasing, and the causal factors producing the intensified glacial cyclicity during the Pliocene must be factors that enhance cooling and climate sensitivity in the subarctic areas.
Resumo:
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.
Resumo:
Continuous sediment sections spanning the last 2.8 Ma have been studied using stable isotope stratigraphy and sedimentological methods. By using paleomagnetic reversals as a chronostratigraphic tool, climatic and paleoceanographic changes have been placed in a time framework. The results show that the major expansion of the Scandinavian Ice Sheet to the coastal areas occurred in the late Neogene period at about 2.8 Ma. Relatively high-amplitude glacials appeared until about 2 Ma. The period between 2.8 and 1.2 Ma was marked by cold surface water conditions with only weak influx of temperate Atlantic water as compared with late Quaternary interglacials. During this period, climatic variations were smaller in amplitude than in the late Quaternary. The Norwegian Sea was a sink of deep water throughout the studied period but deep water ventilation was reduced and calcite dissolution was high compared with the Holocene. Deep water formed by other processes than today. Between 2 and 1.2 Ma, glaciations in Scandinavia were relatively small. A transition toward larger glacials took place during the period 1.2 to 0.6 Ma, corresponding with warmer interglacials and increasing influx of temperate surface water during interglacials. A strong thermal gradient was present between the Norwegian Sea and the northeastern Atlantic during the Matuyama (2.5-0.7 Ma). This is interpreted as a sign of a more zonal and less meridional climatic system over the region as compared with the present situation. The transition towards more meridionality took place over several hundred thousand yr. Only during the last 0.6 Ma has the oceanographic and climatic system of the Norwegian Sea varied in the manner described from previous studies of the late Quaternary.
Resumo:
Stable isotopic compositions of carbon and nitrogen and organic carbon content of sediments ranging from the Pliocene to the Pleistocene-Holocene in age from the Oman Margin (ODP Sites 724 and 725) are reported. In general, the organic carbon content is greater than 2% at Site 724. Prior to the Pleistocene-Holocene at this site, sediments with higher content of organic matter were deposited owing to favorable preservation conditions and/or higher productivity. In the Pleistocene, lower amounts of organic matter have been preserved; this material generally has more enriched nitrogen isotopic compositions. This may indicate intensification of the Oxygen Minimum Zone and denitrification with the onset of the Pleistocene. A correlation of carbon isotope content of these sediments with oxygen isotope stages at Site 724 indicates an enrichment in 13C during glacial events. Based on the stable isotope evidence of both carbon and nitrogen, there does not appear to be major input of terrigenous-derived allochthonous material in this marine environment. The timing and extent of monsoon winds on the productivity of this region are not evident, but require further studies for collaborative interpretation of small-scale features in the isotopic and carbon content of this environment.
Resumo:
Hydrothermal fluids expelled from the seafloor at high and low temperatures play pivotal roles in controlling seawater chemistry. However, the magnitude of the high temperature water flux of mid-ocean ridge axes remains widely disputed and the volume of low temperature vent fluids at ridge flanks is virtually unconstrained. Here, we determine both high and low temperature hydrothermal fluid fluxes using the chemical and isotopic mass balance of the element thallium (Tl) in the ocean crust. Thallium is a unique tracer of ocean floor hydrothermal exchange because of its contrasting behavior during seafloor alteration at low and high temperatures and the distinctive isotopic signatures of fresh and altered MORB and seawater. The calculated high temperature hydrothermal water flux is (0.17-2.93)*10**13 kg/yr with a best estimate of 0.72*10**13 kg/yr. This result suggests that only about 5 to 80% of the heat available at mid-ocean ridge axes from the crystallization and cooling of the freshly formed ocean crust, is released by high temperature black smoker fluids.The residual thermal energy ismost likely lost via conduction and/or through the circulation of intermediate temperature hydrothermal fluids that do not alter the chemical budgets of Tl in the ocean crust. The Tl-based calculations indicate that the low temperature hydrothermal water flux at ridge flanks is (0.2-5.4)*10**17 kg/yr. This implies that the fluids have an average temperature anomaly of only about 0.1 to 3.6 °C relative to ambient seawater. If these low temperatures are correct then both Sr and Mg are expected to be relatively unreactive in ridge-flank hydrothermal systems and this may explain why the extent of basalt alteration that is observed for altered ocean crust appears insufficient to balance the oceanic budgets of 87Sr/86Sr and Mg.
Resumo:
Secondary carbonate minerals were recovered within the basalts at both ODP Sites 768 and 770 in the Sulu and Celebes seas. Petrographic and X-ray diffraction analyses indicate that the carbonates are calcites. Other alteration products recognized in the thin sections are smectites, iron oxides, and gypsum. The 13C values of carbonates from both sites range from 1.6 per mil to 2.3 per mil, which are indicative of inorganic carbonate formation with no contributions from 13C-depleted sources such as oxidized organic carbon or methane. The oxygen isotopes at Site 770 range from 30.8 per mil to 31.6 per mil, which indicates a pervasive circulation of cold seawater (9° to 12°C) during alteration of the Celebes Sea basalts. In contrast, carbonates associated with Site 768 basalts have less positive d18O values (21.0 per mil to 27.3 per mil). A lighter 18O isotopic signature indicates the formation of secondary calcite at either higher temperatures or in a system closed to seawater. The rapidly deposited pyroclastic flows at Site 768 would have limited water access to the crust very soon after its formation, which leads us to speculate that the carbonates in the Sulu Sea basalts were formed by isotopically modified fluids resulting from basalt alteration in a closed system.