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Total individual ion activity coefficients of calcium and carbonate in seawater at 25°C and 35%. salinity,and implications to the agreement between apparent and thermodynamic constants of calcite and aragonite
Authors:LNiel Plummer  Eric T Sundquist
Institution:U.S. Geological Survey, Mail Stop 432, Reston, VA 22092 U.S.A.
Abstract:We have calculated the total individual ion activity coefficients of carbonate and calcium, γTCO32? and γTCa2+, in seawater. Using the ratios of stoichiometric and thermodynamic constants of carbonic acid dissociation and total mean activity coefficient data measured in seawater, we have obtained values which differ significantly from those widely accepted in the literature. In seawater at 25°C and 35%. salinity the (molal) values of γTCO23? and γTCa2+ are 0.038 ± 0.002 and 0.173 ± 0.010, respectively. These values of γTCO32? and γTCa2+ are independent of liquid junction errors and internally consistent with the value γTCl? = 0.651. By defining γTCa2+ and γTCO32? on a common scale (γTCl?), the product γTCa2+γTCO32? is independent of the assigned value of γCl? and may be determined directly from thermodynamic measurements in seawater. Using the value γTCa2+γTCO32? = 0.0067 and new thermodynamic equilibrium constants for calcite and aragonite, we show that the apparent constants of calcite and aragonite are consistent with the thermodynamic equilibrium constants at 25°C and 35%. salinity. The demonstrated consistency between thermodynamic and apparent constants of calcite and aragonite does not support a hypothesis of stable Mg-calcite coatings on calcite or aragonite surfaces in seawater, and suggests that the calcite critical carbonate ion curve of Broecker and Takahashi (1978, Deep-Sea Research25, 65–95) defines the calcite equilibrium boundary in the oceans, within the uncertainty of the data.
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