Non sea-salt sulfate (NSS) of 2.2--2.3 nmol m-3 total magnitude in aerosols observed during the First Aerosol Characterization Experiment (ACE-1) at Cape Grim, Tasmania, was trimodally distributed with ~1-nmol NSS m-3 in >0.7 μm ambient diameter (diam) coarse sea-salt mode aerosols; despite this low NSS concentration, <H2SO4(g)> was so low that 0.7 μm diam aerosols. The mechanism of O3 oxidation of SO2 in sea-salt aerosol water (SSAW) is assessed for its capability to explain this coarse aerosol NSS. Limitation of this mechanism's NSS contribution is largely due to SSAW's buffering capacity since its reaction rate is reduced by 2 orders of magnitude at pH 6 versus the pH≥8 of unreacted SSAW. However, the buffering capacity of sea-salt aerosols may have been significantly enhanced over that of bulk seawater alkalinity. This appears to be due to carbonate resulting from small fragments of biogenic CaCO3 in the ocean's surface microlayer. Given the observed nonsoil calcium excess over that in bulk seawater, the estimated actual buffering capacity of sea-salt aerosols observed during ACE 1 was 50%, or more, enhanced over that due to bulk seawater alkalinity. Considering this enhanced buffering capacity, O3 oxidation of SO2 in SSAW can produce sufficient NSS to explain 70--90% of the ~1 nmol m-3 found in >0.7 μm diam coarse sea-salt aerosols with cloud processing and further oxidation of SO2 in SSAW (i.e., pH<6) by other sea-salt conversion mechanisms contributing the remainder. The amount of NSS produced by sea-salt conversion mechanisms during the ACE 1 remote Southern Ocean experiment vied with homogeneous and cloud processing in their contribution to the total observed NSS of 2.2--2.3 nmol m-3. ¿ 1999 American Geophysical Union