We measured dimethylsulfide in air (DMSa) and the number concentration, size distribution, and chemical composition of atmospheric aerosols, including the concentration of cloud condensation nuclei (CCN), during February‐March 1991 over the tropical South Atlantic along 19°S (F/S Meteor, cruise 15/3). Aerosol number/size distributions were determined with a laser‐optical particle counter, condensation nuclei (CN) concentrations with a TSI 3020, and cloud condensation nuclei (CCN) with a Hudson‐type supersaturation chamber. Aerosol samples were collected on two‐stage stacked filters and analyzed by ion chromatography for soluble ion concentrations. Black carbon in aerosols was measured by visible light absorption and used to identify and eliminate periods with anthropogenic pollution from the data set. Meteorological analysis shows that most of the air masses sampled had spent extended periods over remote marine areas in the tropical and subtropical region. DMSa was closely correlated with the sea‐to‐ air DMS flux calculated from DMS concentrations in seawater and meteorological data. Sea salt made the largest contribution to aerosol mass and volume but provided only a small fraction of the aerosol number concentration. The submicron aerosol had a mean composition close to ammonium bisulfate, with the addition of some methanesulfonate. Aerosol (CN and CCN) number and non‐sea‐salt sulfate concentrations were significantly correlated with DMS concentration and flux. This suggests that DMS oxidation followed by aerosol nucleation and growth in the marine boundary layer is an important, if not dominating, source of CN and possibly CCN. The degree of correlation between DMS and particle concentrations in the marine boundary layer may be strongly influenced by the different time scales of the processes regulating these concentrations. Our results provide strong support for several aspects of the CLAW hypothesis, which proposes the existence of a feedback loop linking DMS emission from marine plankton to sulfate aerosol and global climate.

Recent studies have established that aqueous phase concentrations of dimethylsulfoxide (DMSO) often exceed those of dimethylsulfoniopropionate (DMSP) and dimethylsulfide (DMS). Yet, in comparison to DMSP and DMS, DMSO remains a poorly understood component of the marine sulfur cycle. Much of what is known about the mechanisms for the formation and loss for DMSO is inferred from laboratory experiments, and no explanation exists to rationalize how a large pool of DMSO is maintained. One formation pathway that, until very recently, has been ignored involves the direct synthesis of DMSO by marine phytoplankton. This review examines some of the circumstantial evidence for DMSO in marine particulate material and recent reports containing preliminary data for particulate DMSO (DMSOp) in the marine environment. Drawing on literature from a range of scientific disciplines, speculations on the possible origins and biological functions of intracellular DMSO are also made. On the basis of its physicochemical properties, intracellular DMSO could have a potential role as a cryoprotectant, a specialist cryo‐osmoregulator in extreme environments, an intracellular electrolyte modifier, and a free‐radical scavenger. The review also assesses the impact of DMSOp at both the organism and the global level. Consideration is given to the marine biogeochemical cycling of sulfur and potential links to climate control.

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Two shallow ponds at Cape Evans, Ross Island, were sampled at 1–2 week intervals, during winter freezing throughout the winter and during the subsequent melt period, to examine the physical and chemical conditions imposed on the biota during the year. Liquid water was first detected at the base of the ponds in late December. During the main summer melt period conductivities were less than 10 mS cm−1 with maximum daily temperatures around 5°C. The bottom waters became increasingly saline during freezing and water temperatures decreased below 0°C; by June the remaining water overlying the sediments had conductivities >150 mS cm−1 and temperatures of −13°C. Calcium carbonate, then sodium sulphate precipitated out of solution during early freezing. The dominant nitrogen species was dissolved organic-N which reached 12 g m−3 in Pond 1 just prior to final freeze up. The organic and inorganic forms of nitrogen and dissolved reactive phosphorus increased with increasing conductivity in the ponds. The behaviour of particulate-N and particulate-P mirrored that of chlorophyll a with a peak in March-April and a second higher peak just before final freeze-up. This study provides clear evidence that organisms which persist throughout the year in Antarctic coastal ponds must be capable of surviving much more severe osmotic, pH, temperature and redox conditions than those measured during the summer melt. Deoxygenation, pH decline and H2S production, however, point to continued respiratory activity well into the dark winter months.