Molybdenum Isotope Fingerprinting of Microbial Sulfate Reduction in Seep Carbonate Rocks

Abstract Understanding the interaction between molybdenum (Mo) and organic matter during microbial sulfate reduction is critical for the use of Mo to reconstruct marine redox conditions throughout Earth's history. However, little is known about Mo isotope fractionation and how it relates to org...

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Main Authors: Zice Jia, Yu Hu, Germain Bayon, Jörn Peckmann, Xudong Wang, Shanggui Gong, Jie Li, Harry H. Roberts, Duofu Chen, Dong Feng
Format: Article
Language:English
Published: Wiley 2024-03-01
Series:Geochemistry, Geophysics, Geosystems
Online Access:https://doi.org/10.1029/2023GC011379
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author Zice Jia
Yu Hu
Germain Bayon
Jörn Peckmann
Xudong Wang
Shanggui Gong
Jie Li
Harry H. Roberts
Duofu Chen
Dong Feng
author_facet Zice Jia
Yu Hu
Germain Bayon
Jörn Peckmann
Xudong Wang
Shanggui Gong
Jie Li
Harry H. Roberts
Duofu Chen
Dong Feng
author_sort Zice Jia
collection DOAJ
description Abstract Understanding the interaction between molybdenum (Mo) and organic matter during microbial sulfate reduction is critical for the use of Mo to reconstruct marine redox conditions throughout Earth's history. However, little is known about Mo isotope fractionation and how it relates to organic matter remineralization during microbial sulfate reduction. Here, we report Mo abundances and isotopic (δ98Mo) compositions for bulk‐rock, non‐lithogenic and sequentially extracted fractions, including carbonate (carb), pyrite, and organic matter (OM), of seep carbonate rocks. Our data indicate that the difference between δ98Mocarb and δ98MoOM (Δ98Mocarb‐OM) displays significant variability in the studied samples, ranging between 0.72 and 1.01‰. Remarkably, the obtained Δ98Mocarb‐OM values indicate correlative trends with stable carbon isotope ratios and bulk abundances of (a) total organic carbon, (b) Mo, and (c) pyrite in seep carbonates, which we interpret as reflecting sustained adsorption of isotopically light Mo onto organic matter during enhanced sulfate reduction. On this basis, we put forward the concept that Δ98Mocarb‐OM of authigenic carbonate rocks can be used as a measure of the intensity of sulfate reduction and for reconstructing past interactions between Mo and organic matter in marine sediments.
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spelling doaj.art-a7ce9c64471141be91dd515176d8df542024-04-16T08:35:30ZengWileyGeochemistry, Geophysics, Geosystems1525-20272024-03-01253n/an/a10.1029/2023GC011379Molybdenum Isotope Fingerprinting of Microbial Sulfate Reduction in Seep Carbonate RocksZice Jia0Yu Hu1Germain Bayon2Jörn Peckmann3Xudong Wang4Shanggui Gong5Jie Li6Harry H. Roberts7Duofu Chen8Dong Feng9College of Oceanography and Ecological Science Shanghai Ocean University Shanghai ChinaCollege of Oceanography and Ecological Science Shanghai Ocean University Shanghai ChinaUniversity Brest CNRS Ifremer Geo‐Ocean Plouzané FranceCenter for Earth System Research and Sustainability Institute for Geology Universität Hamburg Hamburg GermanyCollege of Oceanography and Ecological Science Shanghai Ocean University Shanghai ChinaCollege of Oceanography and Ecological Science Shanghai Ocean University Shanghai ChinaState Key Laboratory of Isotope Geochemistry Guangzhou Institute of Geochemistry Chinese Academy of Sciences Guangzhou ChinaCollege of the Coastal and Environment Coastal Studies Institute Louisiana State University Baton Rouge LA USACollege of Oceanography and Ecological Science Shanghai Ocean University Shanghai ChinaCollege of Oceanography and Ecological Science Shanghai Ocean University Shanghai ChinaAbstract Understanding the interaction between molybdenum (Mo) and organic matter during microbial sulfate reduction is critical for the use of Mo to reconstruct marine redox conditions throughout Earth's history. However, little is known about Mo isotope fractionation and how it relates to organic matter remineralization during microbial sulfate reduction. Here, we report Mo abundances and isotopic (δ98Mo) compositions for bulk‐rock, non‐lithogenic and sequentially extracted fractions, including carbonate (carb), pyrite, and organic matter (OM), of seep carbonate rocks. Our data indicate that the difference between δ98Mocarb and δ98MoOM (Δ98Mocarb‐OM) displays significant variability in the studied samples, ranging between 0.72 and 1.01‰. Remarkably, the obtained Δ98Mocarb‐OM values indicate correlative trends with stable carbon isotope ratios and bulk abundances of (a) total organic carbon, (b) Mo, and (c) pyrite in seep carbonates, which we interpret as reflecting sustained adsorption of isotopically light Mo onto organic matter during enhanced sulfate reduction. On this basis, we put forward the concept that Δ98Mocarb‐OM of authigenic carbonate rocks can be used as a measure of the intensity of sulfate reduction and for reconstructing past interactions between Mo and organic matter in marine sediments.https://doi.org/10.1029/2023GC011379
spellingShingle Zice Jia
Yu Hu
Germain Bayon
Jörn Peckmann
Xudong Wang
Shanggui Gong
Jie Li
Harry H. Roberts
Duofu Chen
Dong Feng
Molybdenum Isotope Fingerprinting of Microbial Sulfate Reduction in Seep Carbonate Rocks
Geochemistry, Geophysics, Geosystems
title Molybdenum Isotope Fingerprinting of Microbial Sulfate Reduction in Seep Carbonate Rocks
title_full Molybdenum Isotope Fingerprinting of Microbial Sulfate Reduction in Seep Carbonate Rocks
title_fullStr Molybdenum Isotope Fingerprinting of Microbial Sulfate Reduction in Seep Carbonate Rocks
title_full_unstemmed Molybdenum Isotope Fingerprinting of Microbial Sulfate Reduction in Seep Carbonate Rocks
title_short Molybdenum Isotope Fingerprinting of Microbial Sulfate Reduction in Seep Carbonate Rocks
title_sort molybdenum isotope fingerprinting of microbial sulfate reduction in seep carbonate rocks
url https://doi.org/10.1029/2023GC011379
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