Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone
The strongly 13C-depleted calcite in the Doushantuo cap dolostones (∼635 Ma) of South China is considered to form via thermochemical or biological oxidation of methane by sulfate in an environment with sulfate concentrations close to that of modern seawater (∼28 mM). Here we demonstrate that the coe...
Ausführliche Beschreibung
Autor*in: |
Cai, Chunfang [verfasserIn] Liu, Dawei [verfasserIn] Hu, Yongjie [verfasserIn] Huang, Taiyu [verfasserIn] Jiang, Ziwen [verfasserIn] Xu, Chenlu [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2023 |
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Übergeordnetes Werk: |
Enthalten in: Geochimica et cosmochimica acta - New York, NY [u.a.] : Elsevier, 1950, 346, Seite 245-258 |
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Übergeordnetes Werk: |
volume:346 ; pages:245-258 |
DOI / URN: |
10.1016/j.gca.2023.02.014 |
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Katalog-ID: |
ELV009360042 |
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245 | 1 | 0 | |a Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone |
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520 | |a The strongly 13C-depleted calcite in the Doushantuo cap dolostones (∼635 Ma) of South China is considered to form via thermochemical or biological oxidation of methane by sulfate in an environment with sulfate concentrations close to that of modern seawater (∼28 mM). Here we demonstrate that the coeval seawater sulfate levels were indeed low (∼1 to 3 mM) because all bulk δ34S values of pyrites are close to and higher than the coeval seawater, with only a few showing a wide in situ δ34S range from 5 to 62‰. Such low sulfate concentrations were initially consumed by sulfate reducing microorganisms to extremely low levels (<∼0.2 mM), and thus Mn-driven anaerobic oxidation of methane (AOM) by sulfate occurred in pore water to produce H2S, which was in turn oxidized by Mn oxides back to sulfate. Consequently, with increasing Mn reduction and decreasing sulfate concentrations in pore waters, the produced pyrite shows an increase of in situ δ34S values, and is in association with calcite with more negative δ13C values, and an inherited positive Ce anomaly from Mn oxides. Finally, the pyrite with the highest δ34S value may have co-precipitated with the 13C-depelted calcite (with a nadir of −58‰), and thus show similarly high Mn concentrations (∼20000 μg/g). This is the first report of sulfate-dependent AOM driven by Mn- or Fe- oxides from the entire Precambrian record. Such a previously unrecognized biogeochemical cycling during Marinoan global deglaciation may serve as the mechanism for major methane sink during the Proterozoic and Archean with low sulfate concentrations in the oceans. | ||
650 | 4 | |a Mn-driven AOM | |
650 | 4 | |a Snowball Earth | |
650 | 4 | |a Cryptic sulfur cycle | |
650 | 4 | |a Sulfur isotopes | |
700 | 1 | |a Liu, Dawei |e verfasserin |4 aut | |
700 | 1 | |a Hu, Yongjie |e verfasserin |4 aut | |
700 | 1 | |a Huang, Taiyu |e verfasserin |0 (orcid)0000-0002-1235-6667 |4 aut | |
700 | 1 | |a Jiang, Ziwen |e verfasserin |0 (orcid)0000-0001-8144-9210 |4 aut | |
700 | 1 | |a Xu, Chenlu |e verfasserin |4 aut | |
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allfields |
10.1016/j.gca.2023.02.014 doi (DE-627)ELV009360042 (ELSEVIER)S0016-7037(23)00087-X DE-627 ger DE-627 rda eng 550 DE-600 38.32 bkl 39.29 bkl Cai, Chunfang verfasserin (orcid)0000-0001-7483-2991 aut Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The strongly 13C-depleted calcite in the Doushantuo cap dolostones (∼635 Ma) of South China is considered to form via thermochemical or biological oxidation of methane by sulfate in an environment with sulfate concentrations close to that of modern seawater (∼28 mM). Here we demonstrate that the coeval seawater sulfate levels were indeed low (∼1 to 3 mM) because all bulk δ34S values of pyrites are close to and higher than the coeval seawater, with only a few showing a wide in situ δ34S range from 5 to 62‰. Such low sulfate concentrations were initially consumed by sulfate reducing microorganisms to extremely low levels (<∼0.2 mM), and thus Mn-driven anaerobic oxidation of methane (AOM) by sulfate occurred in pore water to produce H2S, which was in turn oxidized by Mn oxides back to sulfate. Consequently, with increasing Mn reduction and decreasing sulfate concentrations in pore waters, the produced pyrite shows an increase of in situ δ34S values, and is in association with calcite with more negative δ13C values, and an inherited positive Ce anomaly from Mn oxides. Finally, the pyrite with the highest δ34S value may have co-precipitated with the 13C-depelted calcite (with a nadir of −58‰), and thus show similarly high Mn concentrations (∼20000 μg/g). This is the first report of sulfate-dependent AOM driven by Mn- or Fe- oxides from the entire Precambrian record. Such a previously unrecognized biogeochemical cycling during Marinoan global deglaciation may serve as the mechanism for major methane sink during the Proterozoic and Archean with low sulfate concentrations in the oceans. Mn-driven AOM Snowball Earth Cryptic sulfur cycle Sulfur isotopes Liu, Dawei verfasserin aut Hu, Yongjie verfasserin aut Huang, Taiyu verfasserin (orcid)0000-0002-1235-6667 aut Jiang, Ziwen verfasserin (orcid)0000-0001-8144-9210 aut Xu, Chenlu verfasserin aut Enthalten in Geochimica et cosmochimica acta New York, NY [u.a.] : Elsevier, 1950 346, Seite 245-258 Online-Ressource (DE-627)300898797 (DE-600)1483679-8 (DE-576)120883465 0016-7037 nnns volume:346 pages:245-258 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OPC-GGO SSG-OPC-AST GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 38.32 Geochemie 39.29 Theoretische Astronomie: Sonstiges AR 346 245-258 |
spelling |
10.1016/j.gca.2023.02.014 doi (DE-627)ELV009360042 (ELSEVIER)S0016-7037(23)00087-X DE-627 ger DE-627 rda eng 550 DE-600 38.32 bkl 39.29 bkl Cai, Chunfang verfasserin (orcid)0000-0001-7483-2991 aut Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The strongly 13C-depleted calcite in the Doushantuo cap dolostones (∼635 Ma) of South China is considered to form via thermochemical or biological oxidation of methane by sulfate in an environment with sulfate concentrations close to that of modern seawater (∼28 mM). Here we demonstrate that the coeval seawater sulfate levels were indeed low (∼1 to 3 mM) because all bulk δ34S values of pyrites are close to and higher than the coeval seawater, with only a few showing a wide in situ δ34S range from 5 to 62‰. Such low sulfate concentrations were initially consumed by sulfate reducing microorganisms to extremely low levels (<∼0.2 mM), and thus Mn-driven anaerobic oxidation of methane (AOM) by sulfate occurred in pore water to produce H2S, which was in turn oxidized by Mn oxides back to sulfate. Consequently, with increasing Mn reduction and decreasing sulfate concentrations in pore waters, the produced pyrite shows an increase of in situ δ34S values, and is in association with calcite with more negative δ13C values, and an inherited positive Ce anomaly from Mn oxides. Finally, the pyrite with the highest δ34S value may have co-precipitated with the 13C-depelted calcite (with a nadir of −58‰), and thus show similarly high Mn concentrations (∼20000 μg/g). This is the first report of sulfate-dependent AOM driven by Mn- or Fe- oxides from the entire Precambrian record. Such a previously unrecognized biogeochemical cycling during Marinoan global deglaciation may serve as the mechanism for major methane sink during the Proterozoic and Archean with low sulfate concentrations in the oceans. Mn-driven AOM Snowball Earth Cryptic sulfur cycle Sulfur isotopes Liu, Dawei verfasserin aut Hu, Yongjie verfasserin aut Huang, Taiyu verfasserin (orcid)0000-0002-1235-6667 aut Jiang, Ziwen verfasserin (orcid)0000-0001-8144-9210 aut Xu, Chenlu verfasserin aut Enthalten in Geochimica et cosmochimica acta New York, NY [u.a.] : Elsevier, 1950 346, Seite 245-258 Online-Ressource (DE-627)300898797 (DE-600)1483679-8 (DE-576)120883465 0016-7037 nnns volume:346 pages:245-258 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OPC-GGO SSG-OPC-AST GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 38.32 Geochemie 39.29 Theoretische Astronomie: Sonstiges AR 346 245-258 |
allfields_unstemmed |
10.1016/j.gca.2023.02.014 doi (DE-627)ELV009360042 (ELSEVIER)S0016-7037(23)00087-X DE-627 ger DE-627 rda eng 550 DE-600 38.32 bkl 39.29 bkl Cai, Chunfang verfasserin (orcid)0000-0001-7483-2991 aut Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The strongly 13C-depleted calcite in the Doushantuo cap dolostones (∼635 Ma) of South China is considered to form via thermochemical or biological oxidation of methane by sulfate in an environment with sulfate concentrations close to that of modern seawater (∼28 mM). Here we demonstrate that the coeval seawater sulfate levels were indeed low (∼1 to 3 mM) because all bulk δ34S values of pyrites are close to and higher than the coeval seawater, with only a few showing a wide in situ δ34S range from 5 to 62‰. Such low sulfate concentrations were initially consumed by sulfate reducing microorganisms to extremely low levels (<∼0.2 mM), and thus Mn-driven anaerobic oxidation of methane (AOM) by sulfate occurred in pore water to produce H2S, which was in turn oxidized by Mn oxides back to sulfate. Consequently, with increasing Mn reduction and decreasing sulfate concentrations in pore waters, the produced pyrite shows an increase of in situ δ34S values, and is in association with calcite with more negative δ13C values, and an inherited positive Ce anomaly from Mn oxides. Finally, the pyrite with the highest δ34S value may have co-precipitated with the 13C-depelted calcite (with a nadir of −58‰), and thus show similarly high Mn concentrations (∼20000 μg/g). This is the first report of sulfate-dependent AOM driven by Mn- or Fe- oxides from the entire Precambrian record. Such a previously unrecognized biogeochemical cycling during Marinoan global deglaciation may serve as the mechanism for major methane sink during the Proterozoic and Archean with low sulfate concentrations in the oceans. Mn-driven AOM Snowball Earth Cryptic sulfur cycle Sulfur isotopes Liu, Dawei verfasserin aut Hu, Yongjie verfasserin aut Huang, Taiyu verfasserin (orcid)0000-0002-1235-6667 aut Jiang, Ziwen verfasserin (orcid)0000-0001-8144-9210 aut Xu, Chenlu verfasserin aut Enthalten in Geochimica et cosmochimica acta New York, NY [u.a.] : Elsevier, 1950 346, Seite 245-258 Online-Ressource (DE-627)300898797 (DE-600)1483679-8 (DE-576)120883465 0016-7037 nnns volume:346 pages:245-258 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OPC-GGO SSG-OPC-AST GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 38.32 Geochemie 39.29 Theoretische Astronomie: Sonstiges AR 346 245-258 |
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10.1016/j.gca.2023.02.014 doi (DE-627)ELV009360042 (ELSEVIER)S0016-7037(23)00087-X DE-627 ger DE-627 rda eng 550 DE-600 38.32 bkl 39.29 bkl Cai, Chunfang verfasserin (orcid)0000-0001-7483-2991 aut Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The strongly 13C-depleted calcite in the Doushantuo cap dolostones (∼635 Ma) of South China is considered to form via thermochemical or biological oxidation of methane by sulfate in an environment with sulfate concentrations close to that of modern seawater (∼28 mM). Here we demonstrate that the coeval seawater sulfate levels were indeed low (∼1 to 3 mM) because all bulk δ34S values of pyrites are close to and higher than the coeval seawater, with only a few showing a wide in situ δ34S range from 5 to 62‰. Such low sulfate concentrations were initially consumed by sulfate reducing microorganisms to extremely low levels (<∼0.2 mM), and thus Mn-driven anaerobic oxidation of methane (AOM) by sulfate occurred in pore water to produce H2S, which was in turn oxidized by Mn oxides back to sulfate. Consequently, with increasing Mn reduction and decreasing sulfate concentrations in pore waters, the produced pyrite shows an increase of in situ δ34S values, and is in association with calcite with more negative δ13C values, and an inherited positive Ce anomaly from Mn oxides. Finally, the pyrite with the highest δ34S value may have co-precipitated with the 13C-depelted calcite (with a nadir of −58‰), and thus show similarly high Mn concentrations (∼20000 μg/g). This is the first report of sulfate-dependent AOM driven by Mn- or Fe- oxides from the entire Precambrian record. Such a previously unrecognized biogeochemical cycling during Marinoan global deglaciation may serve as the mechanism for major methane sink during the Proterozoic and Archean with low sulfate concentrations in the oceans. Mn-driven AOM Snowball Earth Cryptic sulfur cycle Sulfur isotopes Liu, Dawei verfasserin aut Hu, Yongjie verfasserin aut Huang, Taiyu verfasserin (orcid)0000-0002-1235-6667 aut Jiang, Ziwen verfasserin (orcid)0000-0001-8144-9210 aut Xu, Chenlu verfasserin aut Enthalten in Geochimica et cosmochimica acta New York, NY [u.a.] : Elsevier, 1950 346, Seite 245-258 Online-Ressource (DE-627)300898797 (DE-600)1483679-8 (DE-576)120883465 0016-7037 nnns volume:346 pages:245-258 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OPC-GGO SSG-OPC-AST GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 38.32 Geochemie 39.29 Theoretische Astronomie: Sonstiges AR 346 245-258 |
allfieldsSound |
10.1016/j.gca.2023.02.014 doi (DE-627)ELV009360042 (ELSEVIER)S0016-7037(23)00087-X DE-627 ger DE-627 rda eng 550 DE-600 38.32 bkl 39.29 bkl Cai, Chunfang verfasserin (orcid)0000-0001-7483-2991 aut Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The strongly 13C-depleted calcite in the Doushantuo cap dolostones (∼635 Ma) of South China is considered to form via thermochemical or biological oxidation of methane by sulfate in an environment with sulfate concentrations close to that of modern seawater (∼28 mM). Here we demonstrate that the coeval seawater sulfate levels were indeed low (∼1 to 3 mM) because all bulk δ34S values of pyrites are close to and higher than the coeval seawater, with only a few showing a wide in situ δ34S range from 5 to 62‰. Such low sulfate concentrations were initially consumed by sulfate reducing microorganisms to extremely low levels (<∼0.2 mM), and thus Mn-driven anaerobic oxidation of methane (AOM) by sulfate occurred in pore water to produce H2S, which was in turn oxidized by Mn oxides back to sulfate. Consequently, with increasing Mn reduction and decreasing sulfate concentrations in pore waters, the produced pyrite shows an increase of in situ δ34S values, and is in association with calcite with more negative δ13C values, and an inherited positive Ce anomaly from Mn oxides. Finally, the pyrite with the highest δ34S value may have co-precipitated with the 13C-depelted calcite (with a nadir of −58‰), and thus show similarly high Mn concentrations (∼20000 μg/g). This is the first report of sulfate-dependent AOM driven by Mn- or Fe- oxides from the entire Precambrian record. Such a previously unrecognized biogeochemical cycling during Marinoan global deglaciation may serve as the mechanism for major methane sink during the Proterozoic and Archean with low sulfate concentrations in the oceans. Mn-driven AOM Snowball Earth Cryptic sulfur cycle Sulfur isotopes Liu, Dawei verfasserin aut Hu, Yongjie verfasserin aut Huang, Taiyu verfasserin (orcid)0000-0002-1235-6667 aut Jiang, Ziwen verfasserin (orcid)0000-0001-8144-9210 aut Xu, Chenlu verfasserin aut Enthalten in Geochimica et cosmochimica acta New York, NY [u.a.] : Elsevier, 1950 346, Seite 245-258 Online-Ressource (DE-627)300898797 (DE-600)1483679-8 (DE-576)120883465 0016-7037 nnns volume:346 pages:245-258 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OPC-GGO SSG-OPC-AST GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 38.32 Geochemie 39.29 Theoretische Astronomie: Sonstiges AR 346 245-258 |
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Enthalten in Geochimica et cosmochimica acta 346, Seite 245-258 volume:346 pages:245-258 |
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Cai, Chunfang @@aut@@ Liu, Dawei @@aut@@ Hu, Yongjie @@aut@@ Huang, Taiyu @@aut@@ Jiang, Ziwen @@aut@@ Xu, Chenlu @@aut@@ |
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Cai, Chunfang |
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Cai, Chunfang ddc 550 bkl 38.32 bkl 39.29 misc Mn-driven AOM misc Snowball Earth misc Cryptic sulfur cycle misc Sulfur isotopes Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone |
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550 DE-600 38.32 bkl 39.29 bkl Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone Mn-driven AOM Snowball Earth Cryptic sulfur cycle Sulfur isotopes |
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Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone |
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Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone |
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interlinked marine cycles of methane, manganese, and sulfate in the post-marinoan doushantuo cap dolostone |
title_auth |
Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone |
abstract |
The strongly 13C-depleted calcite in the Doushantuo cap dolostones (∼635 Ma) of South China is considered to form via thermochemical or biological oxidation of methane by sulfate in an environment with sulfate concentrations close to that of modern seawater (∼28 mM). Here we demonstrate that the coeval seawater sulfate levels were indeed low (∼1 to 3 mM) because all bulk δ34S values of pyrites are close to and higher than the coeval seawater, with only a few showing a wide in situ δ34S range from 5 to 62‰. Such low sulfate concentrations were initially consumed by sulfate reducing microorganisms to extremely low levels (<∼0.2 mM), and thus Mn-driven anaerobic oxidation of methane (AOM) by sulfate occurred in pore water to produce H2S, which was in turn oxidized by Mn oxides back to sulfate. Consequently, with increasing Mn reduction and decreasing sulfate concentrations in pore waters, the produced pyrite shows an increase of in situ δ34S values, and is in association with calcite with more negative δ13C values, and an inherited positive Ce anomaly from Mn oxides. Finally, the pyrite with the highest δ34S value may have co-precipitated with the 13C-depelted calcite (with a nadir of −58‰), and thus show similarly high Mn concentrations (∼20000 μg/g). This is the first report of sulfate-dependent AOM driven by Mn- or Fe- oxides from the entire Precambrian record. Such a previously unrecognized biogeochemical cycling during Marinoan global deglaciation may serve as the mechanism for major methane sink during the Proterozoic and Archean with low sulfate concentrations in the oceans. |
abstractGer |
The strongly 13C-depleted calcite in the Doushantuo cap dolostones (∼635 Ma) of South China is considered to form via thermochemical or biological oxidation of methane by sulfate in an environment with sulfate concentrations close to that of modern seawater (∼28 mM). Here we demonstrate that the coeval seawater sulfate levels were indeed low (∼1 to 3 mM) because all bulk δ34S values of pyrites are close to and higher than the coeval seawater, with only a few showing a wide in situ δ34S range from 5 to 62‰. Such low sulfate concentrations were initially consumed by sulfate reducing microorganisms to extremely low levels (<∼0.2 mM), and thus Mn-driven anaerobic oxidation of methane (AOM) by sulfate occurred in pore water to produce H2S, which was in turn oxidized by Mn oxides back to sulfate. Consequently, with increasing Mn reduction and decreasing sulfate concentrations in pore waters, the produced pyrite shows an increase of in situ δ34S values, and is in association with calcite with more negative δ13C values, and an inherited positive Ce anomaly from Mn oxides. Finally, the pyrite with the highest δ34S value may have co-precipitated with the 13C-depelted calcite (with a nadir of −58‰), and thus show similarly high Mn concentrations (∼20000 μg/g). This is the first report of sulfate-dependent AOM driven by Mn- or Fe- oxides from the entire Precambrian record. Such a previously unrecognized biogeochemical cycling during Marinoan global deglaciation may serve as the mechanism for major methane sink during the Proterozoic and Archean with low sulfate concentrations in the oceans. |
abstract_unstemmed |
The strongly 13C-depleted calcite in the Doushantuo cap dolostones (∼635 Ma) of South China is considered to form via thermochemical or biological oxidation of methane by sulfate in an environment with sulfate concentrations close to that of modern seawater (∼28 mM). Here we demonstrate that the coeval seawater sulfate levels were indeed low (∼1 to 3 mM) because all bulk δ34S values of pyrites are close to and higher than the coeval seawater, with only a few showing a wide in situ δ34S range from 5 to 62‰. Such low sulfate concentrations were initially consumed by sulfate reducing microorganisms to extremely low levels (<∼0.2 mM), and thus Mn-driven anaerobic oxidation of methane (AOM) by sulfate occurred in pore water to produce H2S, which was in turn oxidized by Mn oxides back to sulfate. Consequently, with increasing Mn reduction and decreasing sulfate concentrations in pore waters, the produced pyrite shows an increase of in situ δ34S values, and is in association with calcite with more negative δ13C values, and an inherited positive Ce anomaly from Mn oxides. Finally, the pyrite with the highest δ34S value may have co-precipitated with the 13C-depelted calcite (with a nadir of −58‰), and thus show similarly high Mn concentrations (∼20000 μg/g). This is the first report of sulfate-dependent AOM driven by Mn- or Fe- oxides from the entire Precambrian record. Such a previously unrecognized biogeochemical cycling during Marinoan global deglaciation may serve as the mechanism for major methane sink during the Proterozoic and Archean with low sulfate concentrations in the oceans. |
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title_short |
Interlinked marine cycles of methane, manganese, and sulfate in the post-Marinoan Doushantuo cap dolostone |
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