The dominant sink of oceanic calcium carbonate occurs in undersaturated seawater.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41134627.
- Also identified by DOI 10.1073/pnas.2507771122 and PMC identifier 12582267.
- Licence recorded as CC BY-NC-ND.
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Abstract
Calcium carbonate (CaCO<sub>3</sub>) particles formed by marine organisms dissolve in seawater and on the ocean floor, constituting a key component of the global ocean carbon cycle. However, neither the magnitude nor the distribution of CaCO<sub>3</sub> dissolution in the modern oceans is well constrained. Here we diagnose CaCO<sub>3</sub> dissolution rates in major oceanic regions and reconstruct CaCO<sub>3</sub> settling flux using a data-constrained ocean circulation model and observational climatologies of global seawater alkalinity and dissolved oxygen. Our approach distinguishes the effects of ocean circulation and CaCO<sub>3</sub> dissolution on seawater alkalinity and dissolved oxygen, and involves only one free parameter, a restoring timescale, which is constrained by compiling carbonate export rates estimated in the literature. We find that CaCO<sub>3</sub> dissolution in shallow waters (above the saturation horizon of aragonite) is much smaller than some recent estimates. Excluding the upper 114 m of the euphotic zone, the fraction of CaCO<sub>3</sub> dissolution within aragonite saturated waters is only about 16.5 ± 5.5%. About 39.8 ± 4.5% of CaCO<sub>3</sub> dissolution occurs below the aragonite saturation horizon but above the saturation horizon of calcite. The remaining 43.7 ± 3.8% dissolves in the deep ocean in undersaturated seawater. These results suggest that the seawater CaCO<sub>3</sub> saturation state is the primary control on CaCO<sub>3</sub> dissolution in the ocean.