Affiliation:
1. Environmental Physics Institute of Biogeochemistry and Pollutant Dynamics ETH Zurich Zürich Switzerland
Abstract
AbstractThe oceans are acidifying in response to the oceanic uptake of anthropogenic carbon dioxide (CO2) from the atmosphere, yet the global‐scale progression of this acidification has been poorly documented so far by observations. Here, we fill this gap and use an updated version of the in situ and satellite observation‐based product OceanSODA‐ETHZ to determine the trends and drivers of the surface ocean aragonite saturation state (Ωar) and pH = –log([H+]) (total scale) over the last four decades (1982–2021). In the global mean, Ωar and pH declined at rates of −0.071 ± 0.006 decade−1 and −0.0166 ± 0.0010 decade−1, respectively, with the errors of the trends largely reflecting the uncertainties in the reconstructed pH and Ωar fields. These global mean trends are driven primarily by the increase in surface ocean concentration of dissolved inorganic carbon (DIC) in response to the uptake of anthropogenic CO2, but moderated by changes in natural DIC. Surface warming enhances the decrease in pH, accounting for ∼15% of the global trend. The long‐term trends vary substantially across regions and also differ distinctly between pH and Ωar. The highest trends in pH are found in the high latitudes, while Ωar decreases the fastest in the low latitudes. These regional differences are primarily a consequence of regional differences in the ability of the surface ocean to take up and buffer the anthropogenic CO2. Substantial El Niño‐driven interannual variability is superimposed on these trends, with Ωar showing greater variability than pH, resulting in substantially longer time of emergence for Ωar.
Funder
European Space Agency
Horizon 2020 Framework Programme
Publisher
American Geophysical Union (AGU)
Subject
Atmospheric Science,General Environmental Science,Environmental Chemistry,Global and Planetary Change
Cited by
20 articles.
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