Abstract
Calcium carbonate (CaCO3) minerals secreted by marine organisms are abundant in the ocean. These particles settle and the majority dissolves in deeper waters or at the seafloor. Dissolution of carbonates buffers the ocean, but the vertical and regional distribution and magnitude of dissolution are unclear. Here we use seawater chemistry and age data to derive pelagic CaCO3 dissolution rates in major oceanic regions and provide the first data-based, regional profiles of CaCO3 settling fluxes. We find that global CaCO3 export at 300 m depth is 76 ± 12 Tmol yr−1, of which 36 ± 8 Tmol (47%) dissolves in the water column. Dissolution occurs in two distinct depth zones. In shallow waters, metabolic CO2 release and high-magnesium calcites dominate dissolution while increased CaCO3 solubility governs dissolution in deeper waters. Based on reconstructed sinking fluxes, our data indicate a higher CaCO3 transfer efficiency from the surface to the seafloor in high-productivity, upwelling areas than in oligotrophic systems. These results have implications for assessments of future ocean acidification as well as palaeorecord interpretations, as they demonstrate that surface ecosystems, not only interior ocean chemistry, are key to controlling the dissolution of settling CaCO3 particles.
Original language | English |
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Pages (from-to) | 423-428 |
Number of pages | 6 |
Journal | Nature Geoscience |
Volume | 14 |
Issue number | 6 |
DOIs | |
Publication status | Published - Jun 2021 |
Bibliographical note
Funding Information:We thank G. Gebbie for providing the seawater 14C-age dataset. We thank all who contributed to the creation of GLODAPv2. We thank M. P. Humphreys, W. M. Berelson, S. Dong and A. V. Subhas for useful comments on an earlier version of the manuscript and the three journal reviewers for constructive feedback. O.S. and J.J.M. were supported by the Dutch Ministry of Education via the Netherlands Earth System Science Centre (NESSC). A.D. was supported by the Swiss National Science Foundation (#200020_172476) and by the UniBE international 2021 fellowship programme of the University of Bern.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Nature Limited.