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An isolated perfused crab gill preparation was used to test the hypotheses that crab gill carbonic anhydrase (CA) catalyzes the efflux of CO2 from the hemolymph, which lacks the enzyme, to the ambient medium and that the CA is localized on the luminal surface of the basal membrane. It was found that the efflux of CO2 from the internal perfusate was sensitive to the flow rate of the internal perfusate through the gill (and thus the residence time within the gill). The sensitivity of the CO2 efflux to residence time was nearly abolished upon treatment of the gill with an impermeable dextran-bound CA inhibitor. It is concluded that CA present on the luminal surface of the gill epithelium facilitates CO2 excretion by catalyzing the dehydration of the large hemolymph bicarbonate pool to the more diffusible molecular CO. The action of the enzyme is important in maintaining a CO2 gradient between hemolymph and water in a situation where hemolymph PCO2 is normally low, water PCO2 is variable, and the gills themselves are a source of metabolic CO2.

A new method of calculating PCO2 based on mathematical expressions derived from a measured 'Davenport diagram' is described. The measured 'Davenport diagram' is constructed from in vitro buffer curves relating total CO2 to pH at PCO2 levels which adequately encompass the in vivo range of the acid-base status for the species in question. The 'Davenport diagram' is described by three linear equations such that PCO2 can be accurately calculated from in vivo measured CCO2 and pH. The equations are specific for a given species at a given temperature and hemolymph ionic strength, as are the constants in the more classical Henderson-Hasselbalch equation. The accuracy of the method is equal to calculations using the Henderson-Hasselbalch equation with corrected values for pK1' and alpha CO2 and in vivo PCO2 measured directly. This procedure is equally applicable to fluids with dissolved pigments such as hemolymph from freshwater and marine crustaceans and to human blood. The major benefit of this method of calculating PCO2 is that correction nomograms for the constants in the Henderson-Hasselbalch equation are not required.