Anaerobic oxidation of methane and sulfate reduction along the Chilean continental margin |
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Authors: | Tina Treude,Jutta Niggemann,Paul Wintersteller,Antje Boetius,Bo Barker Jø rgensen |
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Affiliation: | 1 Max Planck Institute for Marine Microbiology, Department of Biogeochemistry, Celsiusstrasse 1, 28359 Bremen, Germany 2 NASA Astrobiology Institute, University of Rhode Island, South Ferry Road, Narragansett, RI 02882, USA 3 RF Forschungsschiffahrt GmbH, Blumenthalstrasse 15, 28023 Bremen, Germany 4 Swiss Federal Institute for Environmental Science and Technology, Limnological Research Center, 6047 Kastanienbaum, Switzerland 5 International University Bremen, Research II, Campusring 1, 28759 Bremen, Germany |
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Abstract: | Anaerobic oxidation of methane (AOM) and sulfate reduction (SR) were investigated in sediments of the Chilean upwelling region at three stations between 800 and 3000 m water depth. Major goals of this study were to quantify and evaluate rates of AOM and SR in a coastal marine upwelling system with high organic input, to analyze the impact of AOM on the methane budget, and to determine the contribution of AOM to SR within the sulfate-methane transition zone (SMT). Furthermore, we investigated the formation of authigenic carbonates correlated with AOM. We determined the vertical distribution of AOM and SR activity, methane, sulfate, sulfide, pH, total chlorins, and a variety of other geochemical parameters. Depth-integrated rates of AOM within the SMT were between 7 and 1124 mmol m−2 a−1, effectively removing methane below the sediment-water interface. Single measurements revealed AOM peaks of 2 to 51 nmol cm−3 d−1, with highest rates at the shallowest station (800 m). The methane turnover was higher than in other diffusive systems of similar ocean depth. This higher turnover was most likely due to elevated organic matter input in this upwelling region offering significant amounts of substrates for methanogenesis. SR within the SMT was mostly fuelled by methane. AOM led to the formation of isotopically light DIC (δ13C: −24.6‰ VPDB) and of distinct layers of authigenic carbonates (δ13C: −14.6‰ VPDB). |
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