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Surface ocean pH and buffer capacity: past, present and future
The ocean’s chemistry is changing due to the uptake of anthropogenic carbon dioxide (CO(2)). This phenomenon, commonly referred to as “Ocean Acidification”, is endangering coral reefs and the broader marine ecosystems. In this study, we combine a recent observational seawater CO(2) data product, i.e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901524/ https://www.ncbi.nlm.nih.gov/pubmed/31819102 http://dx.doi.org/10.1038/s41598-019-55039-4 |
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author | Jiang, Li-Qing Carter, Brendan R. Feely, Richard A. Lauvset, Siv K. Olsen, Are |
author_facet | Jiang, Li-Qing Carter, Brendan R. Feely, Richard A. Lauvset, Siv K. Olsen, Are |
author_sort | Jiang, Li-Qing |
collection | PubMed |
description | The ocean’s chemistry is changing due to the uptake of anthropogenic carbon dioxide (CO(2)). This phenomenon, commonly referred to as “Ocean Acidification”, is endangering coral reefs and the broader marine ecosystems. In this study, we combine a recent observational seawater CO(2) data product, i.e., the 6(th) version of the Surface Ocean CO(2) Atlas (1991–2018, ~23 million observations), with temporal trends at individual locations of the global ocean from a robust Earth System Model to provide a high-resolution regionally varying view of global surface ocean pH and the Revelle Factor. The climatology extends from the pre-Industrial era (1750 C.E.) to the end of this century under historical atmospheric CO(2) concentrations (pre-2005) and the Representative Concentrations Pathways (post-2005) of the Intergovernmental Panel on Climate Change (IPCC)’s 5(th) Assessment Report. By linking the modeled pH trends to the observed modern pH distribution, the climatology benefits from recent improvements in both model design and observational data coverage, and is likely to provide improved regional OA trajectories than the model output could alone, therefore, will help guide the regional OA adaptation strategies. We show that air-sea CO(2) disequilibrium is the dominant mode of spatial variability for surface pH, and discuss why pH and calcium carbonate mineral saturation states, two important metrics for OA, show contrasting spatial variability. |
format | Online Article Text |
id | pubmed-6901524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69015242019-12-12 Surface ocean pH and buffer capacity: past, present and future Jiang, Li-Qing Carter, Brendan R. Feely, Richard A. Lauvset, Siv K. Olsen, Are Sci Rep Article The ocean’s chemistry is changing due to the uptake of anthropogenic carbon dioxide (CO(2)). This phenomenon, commonly referred to as “Ocean Acidification”, is endangering coral reefs and the broader marine ecosystems. In this study, we combine a recent observational seawater CO(2) data product, i.e., the 6(th) version of the Surface Ocean CO(2) Atlas (1991–2018, ~23 million observations), with temporal trends at individual locations of the global ocean from a robust Earth System Model to provide a high-resolution regionally varying view of global surface ocean pH and the Revelle Factor. The climatology extends from the pre-Industrial era (1750 C.E.) to the end of this century under historical atmospheric CO(2) concentrations (pre-2005) and the Representative Concentrations Pathways (post-2005) of the Intergovernmental Panel on Climate Change (IPCC)’s 5(th) Assessment Report. By linking the modeled pH trends to the observed modern pH distribution, the climatology benefits from recent improvements in both model design and observational data coverage, and is likely to provide improved regional OA trajectories than the model output could alone, therefore, will help guide the regional OA adaptation strategies. We show that air-sea CO(2) disequilibrium is the dominant mode of spatial variability for surface pH, and discuss why pH and calcium carbonate mineral saturation states, two important metrics for OA, show contrasting spatial variability. Nature Publishing Group UK 2019-12-09 /pmc/articles/PMC6901524/ /pubmed/31819102 http://dx.doi.org/10.1038/s41598-019-55039-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jiang, Li-Qing Carter, Brendan R. Feely, Richard A. Lauvset, Siv K. Olsen, Are Surface ocean pH and buffer capacity: past, present and future |
title | Surface ocean pH and buffer capacity: past, present and future |
title_full | Surface ocean pH and buffer capacity: past, present and future |
title_fullStr | Surface ocean pH and buffer capacity: past, present and future |
title_full_unstemmed | Surface ocean pH and buffer capacity: past, present and future |
title_short | Surface ocean pH and buffer capacity: past, present and future |
title_sort | surface ocean ph and buffer capacity: past, present and future |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901524/ https://www.ncbi.nlm.nih.gov/pubmed/31819102 http://dx.doi.org/10.1038/s41598-019-55039-4 |
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