Lin, Yu-Shih et al. (2012): Towards constraining H (sub 2) concentration in sub-seafloor sediment; a proposal for combined analysis by two distinct approaches

Leg/Site/Hole:
ODP 201
ODP 201 1231
Identifier:
2012-026211
georefid

10.1016/j.gca.2011.11.008
doi

Creator:
Lin, Yu-Shih
University of Bremen, Department of Geosciences, Organic Geochemistry Group, Bremen, Germany
author

Heuer, Verena B.
author

Goldhammer, Tobias
author

Kellermann, Matthias Y.
author

Zabel, Matthias
author

Hinrichs, Kai-Uwe
author

Identification:
Towards constraining H (sub 2) concentration in sub-seafloor sediment; a proposal for combined analysis by two distinct approaches
2012
Geochimica et Cosmochimica Acta
Elsevier, New York, NY, International
77
186-201
Molecular hydrogen (H (sub 2) ) is a central metabolite that couples organic matter degradation and terminal electron-accepting processes. H (sub 2) levels in natural environments are often regulated by microbial syntrophy; therefore, pore-water H (sub 2) concentration is a useful parameter for studying biogeochemical processes in sediments. However, little is known about H (sub 2) concentrations in marine subsurface sediments. Previous studies applying either a headspace equilibration technique or an extraction method for the analysis of pore-water H (sub 2) in deeply buried sediments have generated results that sometimes contradict the principles established based on studies of microbial culture and surface sediments. In this study, we first evaluated and optimized an extraction method, which was then applied in combination with a headspace equilibration method to determine concentrations of pore-water H (sub 2) in subseafloor sediments along a transect of five sites of different water depths and geochemical regimes at the continental margin off Namibia, SE Atlantic. The two methods generated depth profiles with some similarities in curve shape, but the extraction method yielded higher H (sub 2) values than the headspace equilibration technique. By comparing the two data sets with thermodynamic calculations of potential terminal electron-accepting processes, we were able to provide a first evaluation of syntrophic conditions in subseafloor sediment from the perspective of H (sub 2) biogeochemistry. We observed that in the sulfate reduction zone, the H (sub 2) concentrations are higher than the H (sub 2) threshold allowed for the next most favorable terminal metabolism (methanogenesis), suggesting relaxation of coupling between H (sub 2) -producing and H (sub 2) -consuming activities at these depths. In contrast, the H (sub 2) concentrations in the upper methanogenic zone are low enough for methanogens to outcompete CO (sub 2) -reducing acetogens. Our findings suggest the existence of varied extents of syntrophic H (sub 2) coupling in subseafloor sediment. Abstract Copyright (2012) Elsevier, B.V.
English
Serial
Coverage:Geographic coordinates:
North:-12.0100
West:-81.5400East: 13.4000
South:-27.1500

Geochemistry of rocks, soils, and sediments; Oceanography; Africa; aliphatic hydrocarbons; alkanes; Atlantic Ocean; biochemistry; chemical composition; chemical reactions; chromatograms; chromatography; degradation; East Pacific; Equatorial Pacific; geochemistry; hydrocarbons; hydrochemistry; hydrogen; ICP mass spectra; Leg 201; liquid chromatography; marine sediments; mass spectra; mathematical methods; methane; Namibia; Ocean Drilling Program; ocean floors; ODP Site 1231; organic compounds; Pacific Ocean; pore water; prediction; reduction; sea water; sediments; solid phase; South Atlantic; South Pacific; Southeast Atlantic; Southeast Pacific; Southern Africa; spectra; sulfates; total organic carbon; water-rock interaction;

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