12 resultados para Tin oxyhydroxide

em Publishing Network for Geoscientific


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This study presents osmium (Os) isotope and elemental data for cleaned planktic foraminifera, authigenic Fe-Mn oxyhydroxides and pelagic carbonate host sediments from ODP site 758 in the southernmost reaches of the Bay of Bengal. The Os in the bulk sediments appears to be dominantly hydrogeneous (sourced by carbonate and Fe-Mn oxyhydroxide), but variations in this particular core are controlled by the presence of volcanic ash. Fe-Mn oxyhydroxide leachates (of the bulk sediments) from Holocene samples also yield an Os isotope composition close to that of seawater, but the record diverges from that of foraminifera at a depth corresponding to the oxic/post-oxic boundary, suggesting diagenetic mobilization of Os at depths below this. Holocene planktic foraminifera, cleaned using oxidative-reductive techniques, also give Os isotope compositions indistinguishable from modern seawater, but the record obtained for the past 150 kyr shows strong covaraitions of 187Os/188Os with both the local and global oxygen isotope record, with less radiogenic Os isotope compositions during glacial intervals. These results indicate that foraminifera provide a robust record of seawater Os isotope compositions, and comparison of the data obtained here with records from the other major oceans demonstrate global changes in 187Os/188Os over this time interval, while the covariation with oxygen isotopes suggest a process controlling the Os isotope composition that is in phase with global climate cycles. Global excursions to relatively unradiogenic 187Os/188Os during glacial intervals are consistent with decreased input of radiogenic continental material, reflecting cooler temperatures and reduced continental runoff. Modelling indicates that the shift to unradiogenic values during glacial intervals could be caused by an ~30% decrease in the global river flux, with an ~5% change in river composition. If the residence time of Os in the oceans is ~5 ka then the post-glacial recovery to present-day seawater values is consistent with a corresponding increase in the river flux of around 30%. However, if the residence time of Os is closer to 40 ka, as is suggested by the global river flux, then this demands either significant changes in both the riverine Os flux and composition of around 40% and 30%, respectively, that closely follow the oxygen isotope record, or else a short-lived post-glacial pulse of weathering some 75% greater than the steady-state flux. In either case, these results clearly indicate that climatic changes affect both the flux and composition of weathered material delivered to the oceans on glacial-interglacial timescales.

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Concentrations of tin in sea water decreased from estuarine and shelf (0.02-0.04 µg/kg) to surface Atlantic waters (0.009 µg/kg). Mean contents (ppm) in other materials included: ultramafic rocks, 0.8; basalts, 1.7; silicic rocks, 2.5; red clays, 3.4; amphibolites, 1.2. Oceanic ferromanganese deposits contained from 0.2 to 5.8 ppm; tin and cobalt contents were correlated.

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The strength of the North Atlantic Meridional Overturning Circulation during climatically highly variable Marine Isotope Stage (MIS) 3 has attracted much attention in recent years. Here we present high-resolution Nd isotope compositions of past seawater derived from authigenic Fe-Mn oxyhydroxides recovered from drift sediments on the Blake Ridge in the deep western North Atlantic (ODP Leg 172, Site 1060, 3481 m water depth). The data cover the period from 45 to 35 ka BP, tracing circulation changes during major Heinrich iceberg discharge event 4 (H4, ~40-39 ka BP). The Nd isotope record suggests that there was no northern-source water (NSW) mass like modern NADW at the deeper part of Blake Ridge at any time between 45 and 35 ka. This is fundamentally different from the hydrographic situation during the Holocene where NADW extends below 4500 m at this location. The epsilon-Nd of past deep water recorded in the Blake Ridge sediments was least radiogenic during Dansgaard/Oeschger (D/O) Interstadial (IS) 8 (epsilon-Nd = -11.3) and most radiogenic immediately preceding IS 9 (epsilon-Nd = -9.8). More radiogenic compositions were also recorded during H4 (-10.2 <= epsilon-Nd <= -9.9). The Nd isotope variability in MIS 3 matches that of a physical bottom current strength reconstruction from the same location. Neither record follows the pattern of Northern Hemisphere D/O climatic cycles. In our record, reduced mixing with northern source waters started in stadial 12 and lasted until after H4 in stadial 9, followed by a rapid increase in NSW contribution thereafter. This major change in the Nd isotope record predates the iceberg discharge event Heinrich 4 by more than 3 ka indicating a shallowing of the water mass boundary between Glacial North Atlantic Intermediate Water and Southern Source Water beneath. This early change in bottom water properties at the deep Blake Ridge suggests that North Atlantic deep water advection may already have decreased several thousand years before the actual iceberg discharge event and associated freshening of the surface waters in the North Atlantic. The change can thus not be attributed to climatic events in the North Atlantic but may be related to changes in flux of deep water from the South.