999 resultados para OXYGEN-ISOTOPE


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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.

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High-resolution benthic oxygen isotope and dust flux records from Ocean Drilling Program site 659 have been analyzed to extend the astronomically calibrated isotope timescale for the Atlantic from 2.85 Ma back to 5 Ma. Spectral analysis of the delta18O record indicates that the 41-kyr period of Earth's orbital obliquity dominates the Pliocene record. This is shown to be true regardless of fundamental changes in the Earth's climate during the Pliocene. However, the cycles of Sahelian aridity fluctuations indicate a shift in spectral character near 3 Ma. From the early Pliocene to 3 Ma, the periodicities were dominantly precessional (19 and 23 kyr) and remained strong until 1.5 Ma. Subsequent to 3 Ma, the variance at the obliquity period (41 kyr) increased. The timescale tuned to precession suggests that the Pliocene was longer than previously estimated by more than 0.5 m.y. The tuned ages for the magnetic boundaries Gauss/Gilbert and Top Cochiti are about 6-8% older than the ages of the conventional timescale. A major phase of Pliocene northern hemisphere ice growth occurred between 3.15 Ma and 2.5 Ma. This was marked by a gradual increase in glacial Atlantic delta18O values of 1per mil and an increase in amplitude variations by up to 1.5 per mil, much larger than in the Pacific deepwater record (site 846). The first maxima occured in cold stages G6-96 between 2.7 Ma and 2.45 Ma. Prior to 3 Ma, the isotope record is characterized by predominantly low amplitude fluctuations (< 0.7 per mil). When obliquity forcing was at its minimum between 4.15 and 3.6 Ma and during the Kaena interval, delta18O amplitude fluctuations were minimal. From 4.9 to 4.3 Ma, the delta18O values decreased by about 0.5 per mil, reaching a long-term minimum at 4.15 Ma, suggesting higher deepwater temperatures or a deglaciation. Deepwater cooling and/or an increase in ice volume is indicated by a series of short-term delta18O fluctuations between 3.8 and 3.6 Ma.

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Variations in the 18O/16O ratios of marine fossils and microfossils record changes in seawater 18O/16O and temperature and form the basis for global correlation. Relying on previous compilations and new data, this chapter presents oxygen isotope curves for Phanerozoic foraminifera, mollusks, brachiopods, and conodonts, and for Precambrian limestones, dolostones, and cherts. Periodic oxygen-isotopic variations in deep-sea foraminifera define marine isotope stages that, when combined with biostratigraphy and astronomical tuning, provide a late Cenozoic chronostratigraphy with a resolution of several thousand years. Oxygen isotope events of early Cenozoic, Mesozoic, and Paleozoic age serve as chemostratigraphic markers for regional and global correlation. Precambrian oxygen isotope stratigraphy, however, is hampered by the lack of unaltered authigenic marine sediments.

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Stable oxygen and carbon isotope and sedimentological-paleontological investigations supported by accelerator mass spectrometry 14C datings were carried out on cores from north of 85°N in the eastern central Arctic Ocean. Significant changes in accumulation rates, provenance of ice-rafted debris (IRD), and planktic productivity over the past 80,000 years are documented. During peak glacials, i.e., oxygen isotope stages 4 and 2, the Arctic Ocean was covered by sea ice with decreased seasonal variation, limiting planktic productivity and bulk sedimentation rates. In early stage 3 and during Termination I, major deglaciations of the circum-Arctic regions caused lowered salinities and poor oxygenation of central Arctic surface waters. A meltwater spike and an associated IRD peak dated to ~14-12 14C ka can be traced over the southern Eurasian Basin of the Arctic Ocean. This event was associated with the early and rapid deglaciation of the marine-based Barents Sea Ice Sheet. A separate Termination Ib meltwater event is most conspicuous in the central Arctic and is associated with characteristic dolomitic carbonate IRD. This lithology suggests an origin of glacial ice from northern Canada and northern Greenland where lower Paleozoic platform carbonates crop extensively out.

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Many (bio)geochemical processes that bring about changes in sediment chemistry normally begin at the sediment-water interface, continue at depth within the sediment column and may persist throughout the lifetime of sediments. Because of the differential reactivity of sedimentary phosphate phases in response to diagenesis, dissolution/precipitation and biological cycling, the oxygen isotope ratios of phosphate (d18OP) can carry a distinct signature of these processes, as well as inform on the origin of specific P phases. Here, we present results of sequential sediment extraction (SEDEX) analyses combined with d18OP measurements, aimed at characterizing authigenic and detrital phosphate phases in continental margin sediments from three sites (Sites 1227, 1228 and 1229) along the Peru Margin collected during ODP Leg 201. Our results show that the amount of P in different reservoirs varies significantly in the upper 50 m of the sediment column, but with a consistent pattern, for example, detrital P is highest in siliciclastic-rich layers. The d18OP values of authigenic phosphate vary between 20.2 per mil and 24.8 per mil and can be classified into at least two major groups: authigenic phosphate precipitated at/near the sediment-water interface in equilibrium with paleo-water oxygen isotope ratios (d18Ow) and temperature, and phosphate derived from hydrolysis of organic matter (Porg) with subsequent incomplete to complete re-equlibration and precipitated deeper in the sediments column. The d18OP values of detrital phosphate, which vary from 7.7-15.4 per mil, suggest two possible terrigenous sources and their mixtures in different proportions: phosphate from igneous/metamorphic rocks and phosphate precipitated in source regions in equilibrium with d18Ow of meteoric water. More importantly, original isotopic compositions of at least one phase of authigenic phosphates and all detrital phosphates are not altered by diagenesis and other biogeochemical changes within the sediment column. These findings help to understand the origin and provenance of P phases and paleoenvironmental conditions at/near the sediment-water interface, and to infer post-depositional activities within the sediment column.