The air-sea gas exchange rate is important for modeling and verifying ocean CO₂ uptake, but remains subject to considerable uncertainty. The widely assumed quadratic or cubic dependence of the exchange rate on windspeed together with the latitudinal pattern of mean windspeed implies that exchange is much faster at high compared with low latitudes. This should affect the pattern of ocean uptake of bomb carbon-14 as well as the rate of decline of and latitudinal gradients in atmospheric Δ¹⁴CO₂. We evaluate the constraints on the windspeed dependence of the exchange rate offered by available isotopic measurements, discuss the major uncertainties, and suggest observational strategies to reduce these uncertainties.

Measurements of atmospheric O₂/N₂ ratios and CO₂ concentrations can be combined to form the tracer Atmospheric Potential Oxygen (APO), reflecting primarily ocean biogeochemistry and atmospheric circulation. Building on the work of Stephens et al. [1998], we present a new set of APO observations including shipboard collections from the equatorial Pacific. Our data show a smaller interhemispheric gradient than observed in past studies and a substantial APO maximum around the equator. Following a modeling approach developed by Gruber et al. [2001], we compare these observations with APO fields generated by a set of oceanic and atmospheric models. Overall, our model results agree well with observations, but small differences suggest that modeled north-south transport may be too vigorous, air-sea fluxes may be too coarsely resolved in some regions, and seasonal trapping of surface fluxes may be excessive in some model locations.