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Temporal evolution of shallow marine diagenetic environments: Insights from carbonate concretions

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Temporal evolution of shallow marine diagenetic environments: Insights from carbonate concretions. / Lloyd, S.J; Meister , Patrick ; Liu, Bo et al.
In: Geochimica et Cosmochimica Acta, Vol. 351, 15.06.2023, p. 152-166.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Lloyd, SJ, Meister , P, Liu, B, Nichols, N, Corsetti, FA, Berelson, W, Raiswell, R, Hounslow, MW, Shields, G, Waldron, JWF, Westrick-Snapp , B & Hoffman, J 2023, 'Temporal evolution of shallow marine diagenetic environments: Insights from carbonate concretions', Geochimica et Cosmochimica Acta, vol. 351, pp. 152-166. https://doi.org/10.1016/j.gca.2023.04.022

APA

Lloyd, S. J., Meister , P., Liu, B., Nichols, N., Corsetti, F. A., Berelson, W., Raiswell, R., Hounslow, M. W., Shields, G., Waldron, J. W. F., Westrick-Snapp , B., & Hoffman, J. (2023). Temporal evolution of shallow marine diagenetic environments: Insights from carbonate concretions. Geochimica et Cosmochimica Acta, 351, 152-166. https://doi.org/10.1016/j.gca.2023.04.022

Vancouver

Lloyd SJ, Meister P, Liu B, Nichols N, Corsetti FA, Berelson W et al. Temporal evolution of shallow marine diagenetic environments: Insights from carbonate concretions. Geochimica et Cosmochimica Acta. 2023 Jun 15;351:152-166. Epub 2023 May 11. doi: 10.1016/j.gca.2023.04.022

Author

Lloyd, S.J ; Meister , Patrick ; Liu, Bo et al. / Temporal evolution of shallow marine diagenetic environments : Insights from carbonate concretions. In: Geochimica et Cosmochimica Acta. 2023 ; Vol. 351. pp. 152-166.

Bibtex

@article{2142b3530fbc4d1998f256c9135366e2,
title = "Temporal evolution of shallow marine diagenetic environments: Insights from carbonate concretions",
abstract = "Early diagenesis of marine organic matter dramatically impacts Earth{\textquoteright}s surface chemistry by changing the burial potential of carbon and promoting the formation of authigenic mineral phases including carbonate concretions. Marine sediment-hosted carbonate concretions tend to form as a result of microbial anaerobic diagenetic reactions that degrade organic matter and methane, some of which require an external oxidant. Thus, temporal changes in the oxidation state of Earth{\textquoteright}s oceans may impart a first-order control on concretion authigenesis mechanisms through time. Statistically significant variability in concretion carbonate carbon isotope compositions indicates changes in shallow marine sediment diagenesis associated with Earth{\textquoteright}s evolving redox landscape. This variability manifests itself as an expansion in carbon isotope composition range broadly characterized by an increase in maximum and decrease in minimum isotope values through time. Reaction transport modelling helps to constrain the potential impacts of shifting redox chemistry and highlights the importance of organic carbon delivery to the seafloor, marine sulfate concentrations, methane production and external methane influx. The first appearance of conclusively anaerobic oxidation of methane-derived concretions occurs in the Carboniferous and coincides with a Paleozoic rise in marine sulfate. The muted variability recognized in older concretions (and in particular for Precambrian concretions) likely reflects impacts of a smaller marine sulfate reservoir and perhaps elevated marine dissolved inorganic carbon concentrations. Causes of the increase in carbon isotope maximum values through time are more confounding, but may be related to isotopic equilibration of dissolved inorganic carbon with externally derived methane. Ultimately the concretion isotope record in part reflects changes in organic matter availability and marine oxidation state, highlighting connections with the subsurface biosphere and diagenesis throughout geologic time.",
keywords = "Carbonate concretion, Organic carbon, Sulfate, Methanogenesis, Anaerobic oxidation of methane (AOM), Authigenic carbonate",
author = "S.J Lloyd and Patrick Meister and Bo Liu and Nichols Nichols and Corsetti, {Frank A.} and William Berelson and Raiswell Raiswell and Hounslow, {Mark W} and Graham Shields and Waldron, {John W.F.} and Bayne Westrick-Snapp and Jamie Hoffman",
year = "2023",
month = jun,
day = "15",
doi = "10.1016/j.gca.2023.04.022",
language = "English",
volume = "351",
pages = "152--166",
journal = "Geochimica et Cosmochimica Acta",
issn = "0016-7037",
publisher = "Elsevier Limited",

}

RIS

TY - JOUR

T1 - Temporal evolution of shallow marine diagenetic environments

T2 - Insights from carbonate concretions

AU - Lloyd, S.J

AU - Meister , Patrick

AU - Liu, Bo

AU - Nichols, Nichols

AU - Corsetti, Frank A.

AU - Berelson, William

AU - Raiswell, Raiswell

AU - Hounslow, Mark W

AU - Shields, Graham

AU - Waldron, John W.F.

AU - Westrick-Snapp , Bayne

AU - Hoffman, Jamie

PY - 2023/6/15

Y1 - 2023/6/15

N2 - Early diagenesis of marine organic matter dramatically impacts Earth’s surface chemistry by changing the burial potential of carbon and promoting the formation of authigenic mineral phases including carbonate concretions. Marine sediment-hosted carbonate concretions tend to form as a result of microbial anaerobic diagenetic reactions that degrade organic matter and methane, some of which require an external oxidant. Thus, temporal changes in the oxidation state of Earth’s oceans may impart a first-order control on concretion authigenesis mechanisms through time. Statistically significant variability in concretion carbonate carbon isotope compositions indicates changes in shallow marine sediment diagenesis associated with Earth’s evolving redox landscape. This variability manifests itself as an expansion in carbon isotope composition range broadly characterized by an increase in maximum and decrease in minimum isotope values through time. Reaction transport modelling helps to constrain the potential impacts of shifting redox chemistry and highlights the importance of organic carbon delivery to the seafloor, marine sulfate concentrations, methane production and external methane influx. The first appearance of conclusively anaerobic oxidation of methane-derived concretions occurs in the Carboniferous and coincides with a Paleozoic rise in marine sulfate. The muted variability recognized in older concretions (and in particular for Precambrian concretions) likely reflects impacts of a smaller marine sulfate reservoir and perhaps elevated marine dissolved inorganic carbon concentrations. Causes of the increase in carbon isotope maximum values through time are more confounding, but may be related to isotopic equilibration of dissolved inorganic carbon with externally derived methane. Ultimately the concretion isotope record in part reflects changes in organic matter availability and marine oxidation state, highlighting connections with the subsurface biosphere and diagenesis throughout geologic time.

AB - Early diagenesis of marine organic matter dramatically impacts Earth’s surface chemistry by changing the burial potential of carbon and promoting the formation of authigenic mineral phases including carbonate concretions. Marine sediment-hosted carbonate concretions tend to form as a result of microbial anaerobic diagenetic reactions that degrade organic matter and methane, some of which require an external oxidant. Thus, temporal changes in the oxidation state of Earth’s oceans may impart a first-order control on concretion authigenesis mechanisms through time. Statistically significant variability in concretion carbonate carbon isotope compositions indicates changes in shallow marine sediment diagenesis associated with Earth’s evolving redox landscape. This variability manifests itself as an expansion in carbon isotope composition range broadly characterized by an increase in maximum and decrease in minimum isotope values through time. Reaction transport modelling helps to constrain the potential impacts of shifting redox chemistry and highlights the importance of organic carbon delivery to the seafloor, marine sulfate concentrations, methane production and external methane influx. The first appearance of conclusively anaerobic oxidation of methane-derived concretions occurs in the Carboniferous and coincides with a Paleozoic rise in marine sulfate. The muted variability recognized in older concretions (and in particular for Precambrian concretions) likely reflects impacts of a smaller marine sulfate reservoir and perhaps elevated marine dissolved inorganic carbon concentrations. Causes of the increase in carbon isotope maximum values through time are more confounding, but may be related to isotopic equilibration of dissolved inorganic carbon with externally derived methane. Ultimately the concretion isotope record in part reflects changes in organic matter availability and marine oxidation state, highlighting connections with the subsurface biosphere and diagenesis throughout geologic time.

KW - Carbonate concretion

KW - Organic carbon

KW - Sulfate

KW - Methanogenesis

KW - Anaerobic oxidation of methane (AOM)

KW - Authigenic carbonate

U2 - 10.1016/j.gca.2023.04.022

DO - 10.1016/j.gca.2023.04.022

M3 - Journal article

VL - 351

SP - 152

EP - 166

JO - Geochimica et Cosmochimica Acta

JF - Geochimica et Cosmochimica Acta

SN - 0016-7037

ER -