Atmospheric sulfur cycling in the tropical Pacific marine boundary layer (12°S, 135°W): A comparison of field data and model results: 2. Sulfur dioxide

The atmospheric chemistry of sulfur dioxide over the tropical South Pacific Ocean is investigated by using results from field measurements and numerical models. Simultaneous real time measurements of sulfur dioxide and its biogenic precursor dimethylsulfide were made at 12°S, 135°W for a 6‐day period from March 3 through March 9, 1992. The mean SO 2 and DMS mole fractions were 71 ± 56 pmol mol −1 (1σ) and 453 ± 93 pmol mol −1 (1σ) respectively. These concentrations are compared to those predicted by a time‐dependent photochemical box model of the marine boundary layer. Model estimates of the yield of SO 2 from DMS oxidation range from 27% to 54%. Even with low yields, DMS is the dominant source of SO 2 in this region. Estimates of vertical entrainment velocities based on the tropospheric ozone budget suggest that vertical entrainment is a minor source of SO 2 . The relative rates of various loss mechanisms for SO 2 are dry deposition to the sea surface (58%), in‐cloud oxidation (9%), OH oxidation (5%), and uptake by sea‐salt aerosols (28%).