EVALUATION OF OSMIUM ISOTOPES AND IRIDIUM AS PALEOFLUX TRACERS IN PELAGIC CARBONATES

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dc.contributor.author Dalai T.K.
dc.contributor.author Ravizza G.
dc.date.accessioned 2024-04-29T04:07:47Z
dc.date.available 2024-04-29T04:07:47Z
dc.date.issued 2006
dc.identifier https://elibrary.ru/item.asp?id=12091733
dc.identifier.citation Geochimica et Cosmochimica Acta, 2006, 70, 15, 3928-3942
dc.identifier.issn 0016-7037
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/43780
dc.description.abstract New osmium (Os) isotope and platinum group element (PGE) concentration data are used in conjunction with published 3He and Th isotope data to determine the relative proportions of lithogenic, extraterrestrial and hydrogenous iridium (Ir) in a Pacific pelagic carbonate sequence from the Ocean Drilling Program (ODP) Site 806 on the Ontong Java Plateau (OJP). These calculations demonstrate that lithogenic and extraterrestrial contributions to sedimentary Ir budget are minor, while hydrogenous Ir accounts for roughly 85% of the total Ir. Application of analogous partitioning calculations to previously reported data from a North Pacific red clay sequence (LL44-GPC3) yields very similar results. Total Ir burial fluxes at Site 806 and LL44-GPC3 are also similar, 45 and 30 pg cm-2 kyr-1, respectively. Average Ir/3He and Ir/xs230Thinitial ratios calculated from the entire Site 806 data set are similar to those reported earlier for Pacific sites. In general, down-core profiles of Ir, 3He and xs230Thinitial, are not well correlated with one another. However, all three data sets show similar variance and yield sediment mass accumulation rate estimates that agree within a factor of two. While these results indicate that Ir concentration has potential as a point-paleoflux tracer in pelagic carbonates, Ir-based paleoflux estimates are likely subject to uncertainties that are similar to those associated with Co-based paleoflux estimates. Consequently, local calibration of Ir flux in space and time will be required to fully assess the potential of Ir as a point paleoflux tracer. Measured 187Os/188Os of the OJP sediments are systematically lower than the inferred 187Os/188Os of contemporaneous seawater and a clear glacial-interglacial 187Os/188Os variation is lacking. Mixing calculations suggest Os contributions from lithogenic sources are insufficient to explain the observed 187Os/188Os variations. The difference between the 187Os/188Os of bulk sediment and that of seawater is interpreted in terms of subtle contributions of unradiogenic Os carried by particulate extraterrestrial material. Down-core variations of 187Os/188Os with Pt/Ir and Os/Ir also point to contributions from extraterrestrial particles. Mixing calculations for each set of several triplicate analyses suggest that the unradiogenic Os end member cannot be characterized by primary extraterrestrial particles of chondritic composition. It is noteworthy that in efforts aimed at determining the effect of extraterrestrial contributions, 187Os/188Os of pelagic carbonates has greater potential compared to abundances of PGE. An attempt has been made for the first time to estimate sediment mass accumulation rates based on amount of extraterrestrial Os in the OJP samples and previously reported extraterrestrial Os flux. Throughout most of the OJP record, Os isotope-based paleoflux estimates are within a factor of two of those derived using other constant flux tracers. Meaningful flux estimates cannot be made during glacial maxima because the OJP sediments do not record the low 187Os/188Os reported previously. We speculate that this discrepancy may be related to focusing of extraterrestrial particles at the OJP, as has been suggested to explain down-core 3He variations.
dc.subject ACCUMULATION RATE
dc.subject CARBONATE SEDIMENT
dc.subject GLACIAL DEPOSIT
dc.subject GLACIAL-INTERGLACIAL CYCLE
dc.subject IRIDIUM
dc.subject OCEAN DRILLING PROGRAM
dc.subject OSMIUM ISOTOPE
dc.subject SEAWATER
dc.subject TRACER
dc.title EVALUATION OF OSMIUM ISOTOPES AND IRIDIUM AS PALEOFLUX TRACERS IN PELAGIC CARBONATES
dc.type Статья
dc.identifier.doi 10.1016/j.gca.2006.06.002


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