Apparent calcite supersaturation at the ocean surface: Why the present solubility product of pure calcite in seawater does not predict the correct solubility of the salt in nature |
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| Authors: | Robert C Cooke Paul E Kepkay |
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| Institution: | Department of Oceanography, Dalhousie University, Halifax, Nova Scotia B3H 4J1 Canada;Marine Ecology Laboratory, Bedford Institute of Oceanography, Dartmouth, Nova Scotia B2Y 4A2 Canada |
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| Abstract: | It is generally accepted that seawaters near the ocean surface are supersaturated with calcite and that increasing atmospheric CO2 will not overcome this condition until late in the 21st century. These expectations are based on comparisons of the ion activity products (IAPs) of various seawaters to the solubility product (K) of seawater saturated with pure calcite at 1 atm and a given temperature. It has been shown in recent papers, however, that calcites in contact with natural seawater in the surface oceans are not pure, but are magnesian calcite compositions. As a result, the presently accepted values of the solubility product of calcite in seawater cannot be used to obtain a correct, or even a reasonable estimate of the saturation state of sea water relative to either pure or magnesian calcite. Data are presented demonstrating that use of the currently accepted solubility product of calcite in seawater to determine seawater's relative calcite saturation leads to gross overestimates of its extent. |
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