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Since 2004, we have carried out yearly measurements of physicochemical aerosol characteristics onboard research vessels at Southern Hemisphere high latitudes (34–72° S; 45° W–110° E). In this work, we statistically generalize the results from multiyear (2004–2021) measurements in this area of the aerosol optical depth (AOD) of the atmosphere, concentrations of aerosol and equivalent black carbon (EBC), as well as the ionic composition of aerosol. A common regularity was that the aerosol characteristics decreased with increasing latitude up to the Antarctic coast, where the aerosol content corresponded to the global background level. Between Africa and Antarctica, AOD decreased from 0.07 to 0.024, the particle volume decreased from 5.5 to 0.55 µm3/cm3, EBC decreased from 68.1 to 17.4 ng/m3, and the summed ion concentration decreased from 24.5 to 2.5 µg/m3. Against the background of the common tendency of the latitude decrease in aerosol characteristics, we discerned a secondary maximum (AOD and ion concentrations) or a plateau (aerosol and EBC concentrations). The obtained spatial distribution of aerosol characteristics qualitatively agreed with the model-based MERRA-2 reanalysis data, but showed quantitative differences: the model AOD values were overestimated (by 0.015, on average); while the EBC concentrations were underestimated (by 21.7 ng/m3). An interesting feature was found in the aerosol spatial distribution in the region of Antarctic islands: at a distance of 300 km from the islands, the concentrations of EBC decreased on average by 29%, while the aerosol content increased by a factor of 2.5.

We discuss the measurements of black carbon concentrations in the composition of atmospheric aerosol over the seas of the North Atlantic and European sector of the Arctic Ocean (21 expeditions in 2007–2020). The black carbon concentrations were measured by an aethalometer and filter method. The comparison of the two variants of the measurements of the black carbon concentrations showed that the data acceptably agreed and can be used jointly. It is noted that the spatial distribution of black carbon over the ocean is formed under the influence of outflows of air masses from the direction of continents, where the main sources of emission of absorbing aerosol are concentrated. We analyzed the statistical characteristics of black carbon concentrations in five marine regions, differing by the outflows of continental aerosol. The largest black carbon content is a salient feature of the atmosphere of the North and Baltic Seas, surrounded by land: average values of concentrations are 210 ng/m3, and modal values are 75 ng/m3. In other regions (except in the south of the Barents Sea), the average black carbon concentrations are 37–44 ng/m3 (modal concentrations are 18–26 ng/m3). We discuss the specific features of the spatial (latitude-longitude) distributions of black carbon concentrations, relying on ship-based measurements and model calculations (MERRA-2 reanalysis data). A common regularity of the experimental and model spatial distributions of black carbon is that the concentrations decrease in the northern direction and with the growing distance from the continent: from several hundred ng/m3 in the southern part of the North Sea to values below 50 ng/m3 in polar regions of the ocean.