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  • Deep biosphere  (1)
  • Fe isotope  (1)
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  • 1
    Publication Date: 2022-05-25
    Description: Author Posting. © Elsevier B.V., 2008. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Earth and Planetary Science Letters 268 (2008): 110-123, doi:10.1016/j.epsl.2008.01.010.
    Description: The subsurface biosphere in the basaltic ocean crust is potentially of major importance in affecting chemical exchange between the ocean and lithosphere. Alteration of the oceanic crust commonly yields secondary pyrite that are depleted in 34S relative to igneous sulfides. Although these 34S depleted sulfur isotope ratios may point to signatures of biological fractionation, previous interpretations of sulfur isotope fractionation in altered volcanic rocks have relied on abiotic fractionation processes between intermediate sulfur species formed during basalt alteration. Here, we report results for multiple-S isotope (32S,33S,34S) compositions of altered basalts at ODP Site 801 in the western Pacific and provide evidence for microbial sulfate reduction within the volcanic oceanic crust. In-situ ion-microprobe analyses of secondary pyrite in basement rocks show a large range of δ34S values, between –45‰ and 1‰, whereas bulk rock δ34S analyses yield a more restricted range of –15.8 to 0.9‰. These low and variable δ34S values, together with bulk rock S concentrations ranging from 0.02% up to 1.28% are consistent with loss of magmatic primary mono-sulfide and addition of secondary sulfide via microbial sulfate reduction. High-precision multiple-sulfur isotope (32S/33S/34S) analyses suggest that secondary sulfides exhibit mass-dependent equilibrium fractionation relative to seawater sulfate in both δ33S and δ34S values. These relationships are explained by bacterial sulfate reduction proceeding at very low metabolic rates. The determination of the S-isotope composition of bulk altered oceanic crust demonstrates that S-based metabolic activity of subsurface life in oceanic basalt is widespread, and can affect the global S budget at the crust-seawater interface.
    Description: Alt's contribution was supported by NSF OCE-0424558 and OCE-0622949. Rouxel's contribution was supported by NSF OCE-0622982 and Frank and Lisina Hoch Endowed Fund. Ono thanks Agouron Institute and NSF OCE-0753126 for funding. This research used samples and/or data provided by the Ocean Drilling Program. The ODP is sponsored by the US National Science Foundation (NSF) and participating countries under the management of Joint Oceanographic Institutions (JOI).
    Keywords: Sulfur isotopes ; Seafloor weathering ; Deep biosphere ; Oceanic crust ; Sulfur cycle
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
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  • 2
    Publication Date: 2022-05-26
    Description: Author Posting. © The Author(s), 2009. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Earth and Planetary Science Letters 286 (2009): 436-445, doi:10.1016/j.epsl.2009.07.008.
    Description: Multiple S (δ34S and δ33S) and Fe (δ56Fe) isotope analyses of rounded pyrite grains from 3.1 to 2.6 Ga conglomerates of southern Africa indicate their detrital origin, which supports anoxic surface conditions in the Archaean. Rounded pyrites from Meso- to Neoarchaean gold and uranium-bearing strata of South Africa are derived from both crustal and sedimentary sources, the latter being characterised by non-mass dependent fractionation of S isotopes (Δ33S as negative as -1.35‰) and large range of Fe isotope values (δ56Fe between -1.1 and 1.2‰). Most sediment-sourced pyrite grains are likely derived from sulphide nodules in marine organic matter-rich shales, sedimentary exhalites and volcanogenic massive sulphide deposits. Some sedimentary pyrite grains may have been derived from in situ sulphidised Fe-oxides, prior to their incorporation into the conglomerates, as indicated by unusually high positive δ56Fe values. Sedimentary sulphides without significant non-mass dependent fractionation of S isotopes were also present in the source of some conglomerates. The abundance in these rocks of detrital pyrite unstable in the oxygenated atmosphere may suggest factors other than high pO2 as the cause for the absence of significant non-mass dependent fractionation processes in the 3.2 – 2.7 Ga atmosphere. Rounded pyrites from the ca. 2.6 Ga conglomerates of the Belingwe greenstone belt in Zimbabwe have strongly fractionated δ34S, Δ33S and δ56Fe values, the source of which can be traced back to black shale-hosted massive sulphides in the underlying strata. The study demonstrates the utility of combined multiple S and Fe isotope analysis for provenance reconstruction of Archaean sedimentary successions.
    Description: AH acknowledges support by NAI International Collaboration Grant and NRF grant FA2005040400027. AB participation was supported by NSF grant EAR-937 05-45484, NAI award No. NNA04CC09A, and NSERC 938 Discovery grant. Rouxel's contribution was supported by NSF OCE-0622982.
    Keywords: Archaean ; Witwatersrand basin ; Belingwe greenstone belt ; S isotope ; Fe isotope ; Pyrite ; Gold mineralisation
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
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