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Mercury (Hg) is a global pollutant with substantial human health impacts. While most studies focus on atmospheric total Hg (THg) deposition, contributions of methylated Hg (MeHg), including monomethylmercury (MMHg) and dimethylmercury (DMHg), remain poorly understood. To examine this, we use rain and aerosol Hg speciation data and high-resolution surface DMHg measurements, collected on a transect from Alaskan coastal waters to the Bering and Chukchi Seas. We observed a significant fivefold increase in the MeHg:THg fraction in rain and a 10-fold increase for aerosols, closely linked to elevated surface DMHg and the highest DMHg evasion (~9.4 picomoles per square meter per hour) found in upwelling waters near the Aleutian Islands. These data highlight a previously underexplored aspect of MeHg air-sea exchange and its importance to Hg cycling and human health concerns. Our findings emphasize the importance of DMHg evasion by demonstrating that atmospheric MeHg can be transported long distances (~1700 kilometers) in the Arctic, posing risks to human health and ecosystems. 

Abstract We use a tracer method involving the cosmogenic radioisotope beryllium‐7 (half‐life = 53.3 days) to follow the deposition of aerosols and the fate of snow on the MOSAiC ice floe during winter and spring 2019–2020. When examined alongside data from earlier studies in the Arctic Ocean that covered summer and fall, Be‐7 inventories indicate a summertime peak for aerosol Be‐7 deposition fluxes coinciding with seasonal minima boundary‐level aerosol concentrations, which suggests that deposition fluxes are primarily controlled by precipitation. This conclusion is supported by the linear relationship between Be‐7 fluxes and precipitation rates derived from data from the MOSAiC and SHEBA expeditions. Inventories of Be‐7 within the snow column exhibited evidence of significant redistribution. Be‐7 deficits, relative to the flux, were observed in areas of level sea ice while excess Be‐7 was found associated with deformed ice features such as pressure ridges, leading to the following estimates for the distribution of snow on the ice floe in May 2020: 75–93% of the snow mass is found on deformed sea ice with the remainder on level ice. Furthermore, uncertainties associated with measurements of Be‐7 concentrations within the ocean mixed layer would allow for losses of snow through open leads of up to approximately 20% of the flux. Our snow distribution estimates agree with data from repeat snow depth transect measurements. These results suggest that Be‐7 can be a useful tool in studying snow redistribution. 

Abstract The distributions of iodate and iodide were measured along the GEOTRACES GP15 meridional transect at 152°W from the shelf of Alaska to Papeete, Tahiti. The transect included oxygenated waters near the shelf of Alaska, the full water column in the central basin in the North Pacific Basin, the upper water column spanning across seasonally mixed regimes in the north, oligotrophic regimes in the central gyre, and the equatorial upwelling. Iodide concentrations are highest in the permanently stratified tropical mixed layers, which reflect accumulation due to light‐dependent biological processes, and decline rapidly below the euphotic zone. Vertical mixing coefficients (K_z), derived from complementary⁷Be data, enabled iodide oxidation rates to be estimated at two stations. Iodide half‐lives of 3–4 years show the importance of seasonal mixing processes in explaining north‐south differences in the transect, and also contribute to the decrease in iodide concentrations with depth below the mixed layer. These estimated half‐lives are consistent with a recent global iodine model. No evidence was found for significant inputs of iodine from the Alaskan continental margin, but there is a significant enrichment of iodide in bottom waters overlying deep sea sediments from the interior of the basin.