Measurements at the remote marine boundary layer station of Cape Grim, Northwest Tasmania, allow study of the unperturbed background atmosphere. Here we present a continuous data series of nonmethane hydrocarbons (NMHCs), measured in situ and with high sensitivity during the Second Southern Ocean Photochemistry Experiment (SOAPEX 2) during austral summer 1999. Air masses arriving at Cape Grim originate from the Australian continent, Tasmania, and Southern Ocean and Antarctic regions. In Southern Ocean marine boundary layer (MBL) air, C2 and C3 alkanes show a highly uniform abundance (ethane 142¿11.9 parts per trillion by volume (pptv), propane 8.9¿1.7 pptv) at around 4 times lower concentrations than encountered in unpolluted Northern Hemisphere MBL air. The presence of shorter-lived NMHCs in marine air indicates sources of both C4-C6 alkanes and several alkenes in the Southern Ocean. The alkane isomer distributions and abundances are in broad agreement with literature sea-air flux rates. In dynamically stable maritime air, midday maxima in ethene, propene, and isoprene concentrations of a few pptv indicate photochemically driven sources very near to the sea surface. Despite their high reactivity, the impact of these oceanic alkenes on local OH concentrations in remote MBL air is not significant. However, the abundance of isoprene in marine air may significantly elevate formaldehyde above that generated by methane oxidation. ¿ 2001 American Geophysical Union