An assessment of ocean margin anaerobic processes on oceanic alkalinity budget

Recent interest in the ocean’s capacity to absorb atmospheric CO2 and buffer the accompanying “ocean acidification” has prompted discussions on the magnitude of ocean margin alkalinity production via anaerobic processes. However, available estimates are largely based on gross reaction rates or misco...

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Published in:Global Biogeochemical Cycles
Main Authors: Hu, Xinping, Cai, Wei-Jun
Format: Article in Journal/Newspaper
Language:English
Published: Global Biogeochem 2011
Subjects:
Online Access:https://hdl.handle.net/1969.6/95728
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spelling fttexasamucorpus:oai:tamucc-ir.tdl.org:1969.6/95728 2023-10-25T01:42:27+02:00 An assessment of ocean margin anaerobic processes on oceanic alkalinity budget Hu, Xinping Cai, Wei-Jun 2011-07-08 application/pdf https://hdl.handle.net/1969.6/95728 en_US eng Global Biogeochem Hu, X. and Cai, W.-J., 2011. An assessment of ocean margin anaerobic processes on oceanic alkalinity budget. Global Biogeochemical Cycles, GB3003, doi:10.1029/2010GB003859 https://hdl.handle.net/1969.6/95728 Article 2011 fttexasamucorpus https://doi.org/10.1029/2010GB003859 2023-09-25T10:20:01Z Recent interest in the ocean’s capacity to absorb atmospheric CO2 and buffer the accompanying “ocean acidification” has prompted discussions on the magnitude of ocean margin alkalinity production via anaerobic processes. However, available estimates are largely based on gross reaction rates or misconceptions regarding reaction stoichiometry. In this paper, we argue that net alkalinity gain does not result from the internal cycling of nitrogen and sulfur species or from the reduction of metal oxides. Instead, only the processes that involve permanent loss of anaerobic remineralization products, i.e., nitrogen gas from net denitrification and reduced sulfur (i.e., pyrite burial) from net sulfate reduction, could contribute to this anaerobic alkalinity production. Our revised estimate of net alkalinity production from anaerobic processes is on the order of 4–5 Tmol yr−1 in global ocean margins that include both continental shelves and oxygen minimum zones, significantly smaller than the previously estimated rate of 16–31 Tmol yr−1 . In addition, pyrite burial in coastal habitats (salt marshes, mangroves, and seagrass meadows) may contribute another 0.1–1.1 Tmol yr−1 , although their long‐term effect is not yet clear under current changing climate conditions and rising sea levels. Finally, we propose that these alkalinity production reactions can be viewed as “charge transfer” processes, in which negative charges of nitrate and sulfate ions are converted to those of bicarbonate along with a net loss of these oxidative anions. Article in Journal/Newspaper Ocean acidification Texas A&M University - Corpus Christi: DSpace Repository Global Biogeochemical Cycles 25 3 n/a n/a
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collection Texas A&M University - Corpus Christi: DSpace Repository
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description Recent interest in the ocean’s capacity to absorb atmospheric CO2 and buffer the accompanying “ocean acidification” has prompted discussions on the magnitude of ocean margin alkalinity production via anaerobic processes. However, available estimates are largely based on gross reaction rates or misconceptions regarding reaction stoichiometry. In this paper, we argue that net alkalinity gain does not result from the internal cycling of nitrogen and sulfur species or from the reduction of metal oxides. Instead, only the processes that involve permanent loss of anaerobic remineralization products, i.e., nitrogen gas from net denitrification and reduced sulfur (i.e., pyrite burial) from net sulfate reduction, could contribute to this anaerobic alkalinity production. Our revised estimate of net alkalinity production from anaerobic processes is on the order of 4–5 Tmol yr−1 in global ocean margins that include both continental shelves and oxygen minimum zones, significantly smaller than the previously estimated rate of 16–31 Tmol yr−1 . In addition, pyrite burial in coastal habitats (salt marshes, mangroves, and seagrass meadows) may contribute another 0.1–1.1 Tmol yr−1 , although their long‐term effect is not yet clear under current changing climate conditions and rising sea levels. Finally, we propose that these alkalinity production reactions can be viewed as “charge transfer” processes, in which negative charges of nitrate and sulfate ions are converted to those of bicarbonate along with a net loss of these oxidative anions.
format Article in Journal/Newspaper
author Hu, Xinping
Cai, Wei-Jun
spellingShingle Hu, Xinping
Cai, Wei-Jun
An assessment of ocean margin anaerobic processes on oceanic alkalinity budget
author_facet Hu, Xinping
Cai, Wei-Jun
author_sort Hu, Xinping
title An assessment of ocean margin anaerobic processes on oceanic alkalinity budget
title_short An assessment of ocean margin anaerobic processes on oceanic alkalinity budget
title_full An assessment of ocean margin anaerobic processes on oceanic alkalinity budget
title_fullStr An assessment of ocean margin anaerobic processes on oceanic alkalinity budget
title_full_unstemmed An assessment of ocean margin anaerobic processes on oceanic alkalinity budget
title_sort assessment of ocean margin anaerobic processes on oceanic alkalinity budget
publisher Global Biogeochem
publishDate 2011
url https://hdl.handle.net/1969.6/95728
genre Ocean acidification
genre_facet Ocean acidification
op_relation Hu, X. and Cai, W.-J., 2011. An assessment of ocean margin anaerobic processes on oceanic alkalinity budget. Global Biogeochemical Cycles, GB3003, doi:10.1029/2010GB003859
https://hdl.handle.net/1969.6/95728
op_doi https://doi.org/10.1029/2010GB003859
container_title Global Biogeochemical Cycles
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