Dolomite formation in the dynamic deep biosphere: results from the Peru Margin
Dolomite formation in the dynamic deep biosphere: results from the Peru Margin
Early diagenetic dolomite beds were sampled during the Ocean Drilling Programme (ODP) Leg 201 at four reoccupied ODP Leg 112 sites on the Peru continental margin (Sites 1227/684, 1228/680, 1229/681 and 1230/685) and analysed for petrography, mineralogy, ?13C, ?18O and 87Sr/86Sr values. The results are compared with the chemistry, and ?13C and 87Sr/86Sr values of the associated porewater. Petrographic relationships indicate that dolomite forms as a primary precipitate in porous diatom ooze and siliciclastic sediment and is not replacing the small amounts of precursor carbonate. Dolomite precipitation often pre-dates the formation of framboidal pyrite. Most dolomite layers show 87Sr/86Sr-ratios similar to the composition of Quaternary seawater and do not indicate a contribution from the hypersaline brine, which is present at a greater burial depth. Also, the ?13C values of the dolomite are not in equilibrium with the ?13C values of the dissolved inorganic carbon in the associated modern porewater. Both petrography and 87Sr/86Sr ratios suggest a shallow depth of dolomite formation in the uppermost sediment (<30 m below the seafloor). A significant depletion in the dissolved Mg and Ca in the porewater constrains the present site of dolomite precipitation, which co-occurs with a sharp increase in alkalinity and microbial cell concentration at the sulphate–methane interface. It has been hypothesized that microbial ‘hot-spots’, such as the sulphate–methane interface, may act as focused sites of dolomite precipitation. Varying ?13C values from ?15‰ to +15‰ for the dolomite are consistent with precipitation at a dynamic sulphate–methane interface, where ?13C of the dissolved inorganic carbon would likewise be variable. A dynamic deep biosphere with upward and downward migration of the sulphate–methane interface can be simulated using a simple numerical diffusion model for sulphate concentration in a sedimentary sequence with variable input of organic matter. Thus, the study of dolomite layers in ancient organic carbon-rich sedimentary sequences can provide a useful window into the palaeo-dynamics of the deep biosphere.
Carbon isotopes, deep b\iosphere, dolomite, Peru Margin, strontium isotopes, sulphate–methane interface
1007-1031
Meister, Patrick
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McKenzie, Judith A.
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Vasconcelos, Crisogono
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Bernasconi, Stefano
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Frank, Martin
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Gutjahr, Marcus
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Schrag, Daniel P.
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October 2007
Meister, Patrick
0b137df2-0719-4946-9927-7ef2a846b206
McKenzie, Judith A.
189620fe-2c4d-44b7-9c23-601bb3fb5a48
Vasconcelos, Crisogono
b89b5ed0-6e6c-4ae0-bbb1-afdbfeac95f2
Bernasconi, Stefano
8e669bf9-ad72-4845-aacf-acb7fbdba3cb
Frank, Martin
09ec65ac-f62d-41da-86b2-81908973b8a1
Gutjahr, Marcus
5babbbc4-2a1a-48df-a2e3-d87b2483ea9c
Schrag, Daniel P.
5c21604f-e862-4666-8ad5-d2e51c0c2753
Meister, Patrick, McKenzie, Judith A., Vasconcelos, Crisogono, Bernasconi, Stefano, Frank, Martin, Gutjahr, Marcus and Schrag, Daniel P.
(2007)
Dolomite formation in the dynamic deep biosphere: results from the Peru Margin.
Sedimentology, 54 (5), .
(doi:10.1111/j.1365-3091.2007.00870.x).
Abstract
Early diagenetic dolomite beds were sampled during the Ocean Drilling Programme (ODP) Leg 201 at four reoccupied ODP Leg 112 sites on the Peru continental margin (Sites 1227/684, 1228/680, 1229/681 and 1230/685) and analysed for petrography, mineralogy, ?13C, ?18O and 87Sr/86Sr values. The results are compared with the chemistry, and ?13C and 87Sr/86Sr values of the associated porewater. Petrographic relationships indicate that dolomite forms as a primary precipitate in porous diatom ooze and siliciclastic sediment and is not replacing the small amounts of precursor carbonate. Dolomite precipitation often pre-dates the formation of framboidal pyrite. Most dolomite layers show 87Sr/86Sr-ratios similar to the composition of Quaternary seawater and do not indicate a contribution from the hypersaline brine, which is present at a greater burial depth. Also, the ?13C values of the dolomite are not in equilibrium with the ?13C values of the dissolved inorganic carbon in the associated modern porewater. Both petrography and 87Sr/86Sr ratios suggest a shallow depth of dolomite formation in the uppermost sediment (<30 m below the seafloor). A significant depletion in the dissolved Mg and Ca in the porewater constrains the present site of dolomite precipitation, which co-occurs with a sharp increase in alkalinity and microbial cell concentration at the sulphate–methane interface. It has been hypothesized that microbial ‘hot-spots’, such as the sulphate–methane interface, may act as focused sites of dolomite precipitation. Varying ?13C values from ?15‰ to +15‰ for the dolomite are consistent with precipitation at a dynamic sulphate–methane interface, where ?13C of the dissolved inorganic carbon would likewise be variable. A dynamic deep biosphere with upward and downward migration of the sulphate–methane interface can be simulated using a simple numerical diffusion model for sulphate concentration in a sedimentary sequence with variable input of organic matter. Thus, the study of dolomite layers in ancient organic carbon-rich sedimentary sequences can provide a useful window into the palaeo-dynamics of the deep biosphere.
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Published date: October 2007
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Times Cited: 16
Keywords:
Carbon isotopes, deep b\iosphere, dolomite, Peru Margin, strontium isotopes, sulphate–methane interface
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Local EPrints ID: 191649
URI: http://eprints.soton.ac.uk/id/eprint/191649
ISSN: 0037-0746
PURE UUID: 79188481-a1c4-4788-97e5-1302747ce63d
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Date deposited: 23 Jun 2011 08:45
Last modified: 14 Mar 2024 03:45
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Author:
Patrick Meister
Author:
Judith A. McKenzie
Author:
Crisogono Vasconcelos
Author:
Stefano Bernasconi
Author:
Martin Frank
Author:
Marcus Gutjahr
Author:
Daniel P. Schrag
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