Technical Note: Large overestimation of <i>p</i>CO₂ calculated from pH and alkalinity in acidic, organic-rich freshwaters

Abstract

Abstract. Inland waters have been recognized as a~significant source of carbon dioxide (CO2) to the atmosphere at the global scale. Fluxes of CO2 between aquatic systems and the atmosphere are calculated from the gas transfer velocity and the water-air gradient of the partial pressure of CO2 (pCO2). Nowadays, direct measurements of water pCO2 remain scarce in freshwaters and most published pCO2 data are calculated from temperature, pH and total alkalinity (TA). Here, we compare calculated (pH and TA) and measured (Equilibrator and headspace) water pCO2 in a large array of temperate and tropical freshwaters. The 761 data points cover a wide range of values for TA (0 to 14.2 mmol L−1), pH (3.94 to 9.17), measured pCO2 (36 to 23 000 ppmv), and dissolved organic carbon (DOC) (29 to 3970 μmol L−1). Calculated pCO2 were > 10% higher than measured pCO2 in 60% of the samples (with a median overestimation of calculated pCO2 compared to measured pCO2 of 2560 ppmv) and were > 100% higher in the 25% most organic-rich and acidic samples (with a median overestimation of 9080 ppmv). We suggest these large overestimations of calculated pCO2 with respect to measured pCO2 are due to the combination of two cumulative effects: (1) a more significant contribution of organic acids anions to TA in waters with low carbonate alkalinity and high DOC concentrations; (2) a lower buffering capacity of the carbonate system at low pH, that increases the sensitivity of calculated pCO2 to TA in acidic and organic-rich waters. We recommend that regional studies on pCO2 should not be based on pH and TA data only, and that direct measurements of pCO2 should become the primary method in inland waters in general, and in particular in acidic, poorly buffered, freshwaters.