The atmospheric circulation plays a critical role in the global transport and deposition of atmospheric pollutants such as mercury (Hg). Desert dust emissions contribute to nearly 60-95% of the global dust budget and thus, desert dust may facilitate atmospheric Hg transport and deposition to the downwind regions worldwide. The role of desert dust in biogeochemical cycling of Hg, however, has not been well recognized by the Hg research community. In this study, we measured the concentration of particulate bound Hg (HgP) in total suspended particulate (TSP) collected from China's largest desert, Taklimakan Desert, between 2013 and 2017. The results show that HgP concentrations over the Taklimakan Desert atmosphere are remarkably higher than those observed from background sites in China and are even comparable to those measured in most of the Chinese metropolitan cities. Moreover, HgP concentrations in the Taklimakan Desert exhibit a distinct seasonal pattern peaking during dust storm outbreak periods in spring and summer (March to August). A preliminary estimation demonstrates that export of total Hg associated with atmospheric dust from the Taklimakan Desert could be 59.7 +/- 60.3 (1SD) Mg yr(-1). The unexpectedly high HgP concentrations during duststorms, together with consistent seasonal pattern of Hg revealed from the snow/ice, clearly demonstrate that Asian desert dust could act as a significant carrier of atmospheric Hg to the cryosphere of Western China and even can have further global reach. (C) 2020 Elsevier Ltd. All rights reserved.

Mercury (Hg) is among the most toxic metals possessing a major threat to human health and aquatic ecosystems over the globe. However, measurement of Hg concentrations and seasonal variability remain poorly understood over the IndoGangetic Plain (IGP) in northern India. In this study, we present one-year data of particulate-bound mercury (HgP) in aerosol samples (PM10) collected from Kanpur to understand seasonal variability and factors influencing concentration, as well as dry deposition flux. The HgP concentration exhibit a large temporal variability and ranged between 100 (on 14 June 2007) to 4340 pg m(-3) (on 4 March 2007) with an annual average concentration of HgP is 776 +/- 846 pg m(-3). The HgP concentrations and HgP/PM10 ratios showed a marked seasonality with the highest in winter (Dec-Feb) followed by post-monsoon (Oct-Nov) and summer (April-June) seasons. HgP and HgP/PM10 were positively correlated (r(2) = 0.77, p < 0.05, N = 58) during the sampling period and the estimated dry deposition flux of HgP was 104.7 mu g m(-2) y(-1). Although this study provides a comprehensive data set on HgP in an urban atmosphere of the IGP revealing high levels of HgP, measurement of gaseous Hg is needed for estimation of the total Hg budget. Therefore, future studies should focus on identification of different sources as well as emission characteristics of all forms of Hg (organic and inorganic forms) for better mitigation strategy to prevent health risks associated with toxic Hg in the region.