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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. 

This dataset reports Beryllium-7 concentrations from water samples collected on the MOSAiC expedition, PS122, aboard R/V Polarstern in the Central Arctic Ocean during 2019-2020. 

Naturally formed forest patches known as tree islands are found within lower-statured wetland matrices throughout the world, where they contrast sharply with the surrounding vegetation. In some coastal wetlands they are embedded in former freshwater marshes that are currently exposed to saltwater intrusion and mangrove encroachment associated with accelerating sea-level rise. In this study we resurveyed tree composition and determined environmental conditions in tree islands of the coastal Florida Everglades that had been examined two decades earlier. We asked whether tree islands in this coastal transition zone were differentiated geomorphologically as well as compositionally, and whether favorable geomorphology enabled coastal forest type(s) to maintain their compositional integrity against rising seas. Patterns of variation in geomorphology and soils among forest types were evident, but were dwarfed by differences between forest and adjacent wetlands. Tree island surfaces were elevated by 12–44 cm, and 210Pb analyses indicated that their current rates of vertical accretion were more rapid than those of surrounding ecosystems. Tree island soils were deeper and more phosphorus-rich than in the adjoining matrix. Salinity decreased interiorward in both tree island and marsh, but porewater was fresher in forest than marsh in Mixed Swamp Forest, midway along the coastal gradient where tropical hardwoods were most abundant. Little decrease in the abundance of tropical hardwood species nor increase in halophytes was observed during the study period. Our data suggest that geomorphological differences between organic tree island and marl marsh, perhaps driven by groundwater upwelling through more transmissive tree island soils, contributed to the forests’ compositional stability, though this stasis may be short-lived despite management efforts. 

Abstract Atmospheric deposition of aerosols transported from the continents is an important source of nutrient and pollutant trace elements (TEs) to the surface ocean. During the U.S. GEOTRACES GP15 Pacific Meridional Transect between Alaska and Tahiti (September–November 2018), aerosol samples were collected over the North Pacific and equatorial Pacific and analyzed for a suite of TEs, including Al, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, and Pb. Sampling coincided with the annual minimum in dust transport from Asia, providing an opportunity to quantify aerosol TE concentrations and deposition during the low dust season. Nevertheless, peak concentrations of “crustal” TEs measured at ∼40–50°N (∼145 pmol/m³Fe) were associated with transport from northern Asia, with lower concentrations (36 ± 14 pmol/m³Fe) over the equatorial Pacific. Relative to crustal abundances, equatorial Pacific aerosols typically had higher TE enrichment factors than North Pacific aerosols. In contrast, aerosol V was more enriched over the North Pacific, presumably due to greater supply to this region from oil combustion products. Bulk deposition velocity (V_bulk) was calculated along the transect using the surface ocean decay inventory of the naturally occurring radionuclide,⁷Be, and aerosol⁷Be activity. Deposition velocities were significantly higher (4,570 ± 1,146 m/d) within the Intertropical Convergence Zone than elsewhere (1,764 ± 261 m/d) due to aerosol scavenging by intense rainfall. Daily deposition fluxes to the central Pacific during the low dust season were calculated using V_bulkand aerosol TE concentration data, with Fe fluxes ranging from 19 to 258 nmol/m²/d. 

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. 

Abstract Deposition of aerosols to the surface ocean is an important factor affecting primary production in the surface ocean. However, the sources and fluxes of aerosols and associated trace elements remain poorly defined. Aerosol²¹⁰Pb,²¹⁰Po, and⁷Be data were collected on US GEOTRACES cruise GP15 (Pacific Meridional Transect, 152°W; 2018).²¹⁰Pb fluxes are low close to the Alaskan margin, increase to a maximum at ∼43°N, then decrease to lower values. There is good agreement between²¹⁰Pb fluxes and long‐term land‐based fluxes during the SEAREX program (1970–1980s), as well as between GP15 and GP16 (East Pacific Zonal Transect, 12°S; 2013) at adjacent stations. A normalized fractionf(⁷Be,²¹⁰Pb) is used to discern aerosols with upper (highf) versus lower (lowf) troposphere sources. Alaskan/North Pacific aerosols show significant continental influence while equatorial/South Pacific aerosols are supplied to the marine boundary layer from the upper troposphere. Lithogenic trace elements Al and Ti show inverse correlations withf(⁷Be,²¹⁰Pb), supporting a continental boundary layer provenance while anthropogenic Pb shows no clear relationship withf(⁷Be,²¹⁰Pb). All but four samples have²¹⁰Po/²¹⁰Pb activity ratios <0.2 suggesting short aerosol residence time. Among the four samples (²¹⁰Po/²¹⁰Pb = 0.42–0.88), two suggest an upper troposphere source and longer aerosol residence time while the remaining two cannot be explained by long aerosol residence time nor a significant component of dust. We hypothesize that enrichments of²¹⁰Po in them are linked to Po enrichments in the sea surface microlayer, possibly through Po speciation as a dissolved organic or dimethyl polonide species.