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Long-term monitoring of atmospheric aerosols and their interaction with radiation, cloud, and cryosphere over the Arctic and the Antarctic are very important for the global climate change related issues. In this regard, for conducting aerosol measurements, India has extended the concerted efforts to the Svalbard region of the Norwegian Arctic (Himadri, 78°55′N 11°56′E, 8 m a.s.l.) in the northern hemisphere and the Larsemann Hills of coastal Antarctic (Bharati, 69°24.4′S 76°11.7′E, 40 m a.s.l.) in the southern hemisphere. In the present study, we have examined the role of black carbon (BC) deposition in darkening the polar snow in different sunlit seasons and estimated the scavenging ratio of BC over both the poles from simultaneous measurements of atmospheric and snow deposited BC concentrations. The study reveals distinct spatio-temporal variability of BC in polar snow, even though the concentrations are, in general, low (<12 ppbw, parts per billion by weight). During local summer seasons, the BC in snow at the Arctic (median ∼ 7.98 ppbw) was higher than that at the Antarctica (median ∼ 1.70 ppbw). Concurrent with this, the scavenging ratio (SR) also showed large variability over both the poles. Relatively higher values of SR over the Antarctica (mean ∼ 119.54 ± 23.04; during southern hemispheric summer) in comparison to that over the Arctic (mean ∼ 69.48 ± 4.79; during northern hemispheric spring) clearly indicate the difference in removal mechanisms (aerosol mixing, aging and size distribution) of BC from the atmosphere over distinct polar environments. Measurement of spectral incoming and reflected radiances over the Arctic snow during the early spring season of 2017 indicated the values of surface broadband albedo varying between 0.64 and 0.79. The Snow, Ice and Aerosol Radiative (SNICAR) model simulated values of spectral albedo correlated well with the measured ones and indicated the role of dust absorption, in addition to that of BC, in changing the snow albedo. This information needs to be accurately incorporated in the radiative transfer models for the accurate estimation of snow albedo forcing over the Polar Regions. [ABSTRACT FROM AUTHOR]

In view of the climate impact of aerosol Black Carbon (BC) over snow covered regions (through enhanced absorption of radiation as well as snow-albedo forcing), and in view of the increasing anthropogenic presence and influence in the northern polar regions, continuous long term measurements of airborne BC have been undertaken from the Svalbard region of Norwegian Arctic (Ny-Ålesund, 79°N, 12°E, 8 m a.s.l.). This study, employing data over a period of 4-years (2010–2013) have shown a consistent spring-time enhancement in BC concentrations, having a (climatological) seasonal mean value of ∼50.3 ± 19.5 ng m −3 , nearly 3-times higher than the lowest BC concentrations in summer (∼19.5 ± 6.5 ng m −3 ). Spectral variation of absorbance indicates that long-range transported biomass burning aerosols contribute as high as 25% to the high BC concentrations in the Arctic atmosphere in spring. Concurrent estimates of BC concentrations in the Arctic snow (for an ensemble of snow samples collected over a period of time during spring) showed values ranging from 0.6 ppb to 4.1 ppb. These values have been used to estimate the BC scavenging ratio (SR). Our studies revealed a mean value of SR ∼98 ± 46, which varied over wide range from 40 to 184 for individual samples. In a broader perspective, the seasonal variations of atmospheric BC concentrations at the Arctic are similar to those seen at the high altitude Himalayas; even though the concentrations are much lower at Arctic. It is found that synoptic conditions mainly influence the high altitude Himalayas, while the influences of local anthropogenic influences are not negligible at the Arctic in modulating the seasonal variations of absorbing aerosols. [ABSTRACT FROM AUTHOR]