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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. 

The distribution and cycling of biogenic silica (BSi) and lithogenic silicon (LSi) in the ocean play crucial roles in the global silicon cycle and marine ecosystem dynamics. This is especially the case in the Southern Ocean where diatoms constitute the predominant phytoplankton and participate in a major way to the biological carbon pump. This study presents an assessment of BSi and LSi concentrations along the GEOTRACES South West Indian Ocean Section (SWINGS, late austral summer 2021), where several and contrasting regions were encountered: oligotrophic Mozambique basin, HNLC (High Nutrient Low Chlorophyll) areas and regions fertilized by the Subantarctic islands. Suspended particles were sampled from Niskin bottles and in situ pumps, along with scanning electron microscope (SEM) observations and specific pigments measurements to support BSi and LSi analyses. With samples coming from a contrasting study area prone to diverse continental influences, our BSi and LSi results showed a reproducibility of 13 ± 7%, in the same range as the established protocol. BSi concentrations show a north-south gradient with maxima encountered in the Antarctic Zone, and contrasted results between HNLC open ocean areas and naturally fertilized regions in the vicinity of the Subantarctic islands. Some open ocean stations have unusually high BSi (e.g. > 5 μmol L􀀀 1) likely resulting from fertilization by aerosols, upwelling or island mass effect when they are downstream of the islands. Coupling of BSi with SEM observations and pigments measurements respectively showed diatoms were the most representative of the carrying phase of BSi and suggested silicification changes, induced either by heavily silicified diatoms or by micronutrient limitation in HNLC regions. BSi is often dominated by the smallest size fraction (0.45–5 μm) which represent 47 ± 23% of the total BSi based on 29 measurements on size fractionated samples. LSi results highlighted atmospheric inputs at the surface and nepheloid layers in the water column, which makes LSi overall a good indicator of the origin of lithogenic materials. SEM observations supported these results, enabling characterization of the diversity of lithogenic materials in the vicinity of the Subantarctic islands, more specifically volcanic ash around Heard Island, and within the nepheloid layers. 

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 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 Despite the Pacific being the location of the earliest seawater Cd studies, the processes which control Cd distributions in this region remain incompletely understood, largely due to the sparsity of data. Here, we present dissolved Cd and δ¹¹⁴Cd data from the US GEOTRACES GP15 meridional transect along 152°W from the Alaskan margin to the equatorial Pacific. Our examination of this region's surface ocean Cd isotope systematics is consistent with previous observations, showing a stark disparity between northern Cd‐rich high‐nutrient low‐chlorophyll waters and Cd‐depleted waters of the subtropical and equatorial Pacific. Away from the margin, an open system model ably describes data in Cd‐depleted surface waters, but atmospheric inputs of isotopically light Cd likely play an important role in setting surface Cd isotope ratios (δ¹¹⁴Cd) at the lowest Cd concentrations. Below the surface, Southern Ocean processes and water mass mixing are the dominant control on Pacific Cd and δ¹¹⁴Cd distributions. Cd‐depleted Antarctic Intermediate Water has a far‐reaching effect on North Pacific intermediate waters as far as 47°N, contrasting with northern‐sourced Cd signatures in North Pacific Intermediate Water. Finally, we show that the previously identified negative Cd* signal at depth in the North Pacific is associated with the PO₄maximum and is thus a consequence of an integrated regeneration signal of Cd and PO₄at a slightly lower Cd:P ratio than the deep ocean ratio (0.35 mmol mol⁻¹), rather than being related to in situ removal processes in low‐oxygen waters. 

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.