Search for: All records

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 Atmospheric deposition is an important pathway for delivering micronutrient and pollutant trace elements (TEs) to the surface ocean. In the central Arctic, much of this supply takes place onto sea ice during winter, before eventual delivery to the ocean during summertime melt. However, the seasonality of aerosol TE loading, solubility, and deposition flux are poorly studied over the Arctic Ocean, due to the difficulties of wintertime sampling. As part of the Multidisciplinary drifting Observatory for the Study of Arctic Climate (MOSAiC) expedition, aerosols collected during winter and spring (December–May) were analyzed for soluble, labile, and total TE concentrations. Despite low dust loading, mineral aerosol accounted for most of the variation in total Fe, Al, Ti, V, Mn, and Th concentrations. In contrast, soluble TE concentrations were more closely linked to non‐sea‐salt sulfate, and Fe solubility was significantly higher during Arctic winter (median = 6.5%) than spring (1.9%), suggesting an influence from Arctic haze. Beryllium‐7 data were used to calculate an average bulk deposition velocity of 613 ± 153 m d⁻¹over most of the study period, which was applied to calculate seasonal deposition fluxes of total, labile, and soluble TEs to the central Arctic. Total TE fluxes (173 ± 145 nmol m⁻² d⁻¹for Fe) agreed within a factor of two or three with earlier summertime estimates, with generally higher wintertime concentrations offset by a lower deposition velocity. Cumulative seasonal deposition of total, labile, and soluble Fe to the central Arctic Ocean was calculated at 25 ± 21, 5 ± 3, and 2 ± 2 μmol m⁻², respectively. 

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.