The Greenland Ice Sheet is currently not accounted for in Arctic mercury budgets, despite large and increasing annual runoff to the ocean and the socio-economic concerns of high mercury levels in Arctic organisms. Here we present concentrations of mercury in meltwaters from three glacial catchments on the southwestern margin of the Greenland Ice Sheet and evaluate the export of mercury to downstream fjords based on samples collected during summer ablation seasons. We show that concentrations of dissolved mercury are among the highest recorded in natural waters and mercury yields from these glacial catchments (521–3,300 mmol km−2 year−1) are two orders of magnitude higher than from Arctic rivers (4–20 mmol km−2 year−1). Fluxes of dissolved mercury from the southwestern region of Greenland are estimated to be globally significant (15.4–212 kmol year−1), accounting for about 10% of the estimated global riverine flux, and include export of bioaccumulating methylmercury (0.31–1.97 kmol year−1). High dissolved mercury concentrations (~20 pM inorganic mercury and ~2 pM methylmercury) were found to persist across salinity gradients of fjords. Mean particulate mercury concentrations were among the highest recorded in the literature (~51,000 pM), and dissolved mercury concentrations in runoff exceed reported surface snow and ice values. These results suggest a geological source of mercury at the ice sheet bed. The high concentrations of mercury and its large export to the downstream fjords have important implications for Arctic ecosystems, highlighting an urgent need to better understand mercury dynamics in ice sheet runoff under global warming.

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<p>The accelerated melting of the Greenland Ice Sheet could potentially enhance fluxes of key nutrients, to the surrounding oceans, impacting marine biogeochemical processes and ecosystems. Iron (Fe) is one key micronutrient for marine phytoplankton that may be affected by this increase in meltwater flux, with high export of dissolved and particulate Fe from glacial meltwaters into fjords and a potentially significant increase in the supply of labile and potentially bioavailable Fe to the Greenlandic shelf. However, biogeochemical processing within estuarine-like fjord systems may result in depletion of nutrients, acting as a sink of micronutrients before they can reach the coastal ocean. The extent to which glacially derived micronutrients, specifically Fe, reach coastal waters remains an unanswered question.</p><p>Here, we address this question by assessing the concentration of dissolved (<0.45 µm) and labile particulate (determined using the Berger leach) bio-essential trace metals (Fe, Cd, Mn, Ni, Cu, Zn) in two contrasting glaciated fjords in southwest Greenland; one fed predominantly by marine terminating glaciers and the other by a land terminating glacier. We investigate the difference in size fractionated concentrations between fjords and the transport of these metals from stations close to glacial termini down to the fjord mouths. Our findings reveal that each micronutrient exhibits a distinctive behaviour, with some metals enhanced in meltwaters (e.g. dissolved Fe and Mn) and some depleted (e.g. dissolved Cd), relative to marine waters. The spatial variability in our dataset highlights that concentration of Fe and other trace metals (Cd, Mn, Ni, Cu, Zn) enriched in meltwaters become depleted towards the mouth of the fjords, with non-conservative loss from surface waters. Despite this depletion, the concentrations of these metals in waters that reach the coastal zone are significantly higher than typical surface ocean values, both in dissolved and labile particulate form. These data can ultimately be used in combination with a physical understanding of the fjord systems to constrain the capacity of fjords to enhance productivity downstream and deliver micronutrients into coastal and open ocean systems. Furthermore, the direct comparison of land- and marine-terminating glacial fjords could provide valuable information on the potential future impact of retreating glacial systems with enhanced melting.</p>

<p>Biogeochemical cycling of silicon (Si) in the high latitudes has an important influence on the marine Si budget. The Barents Sea is divided aproximately equally into Arctic and Atlantic water (ArW and AW respectively) domains.  However, increases in the temperature and inflow of AW across the Barents Sea opening is driving an expansion of the AW realm. While the sensitivity of pelagic processes pertaining to primary production is receiving increasingly more attention, less is known of the effect on the benthic Si cycle. This knowledge gap could prove integral, as the flux of Si across the sediment-water interface (SWI) from Arctic shelf sediments could be up to 20% higher than that of riverine sources. This benthic flux is largely controlled by early diagenetic processes in sediment pore waters, including biogenic silica (bSi) dissolution and authigenic precipitation.</p><p>To improve our understanding of benthic Si dynamics in the Barents Sea and examine its sensitivity to future change, we analysed pore water and sediment samples from both the AW and ArW realms between 2017-2019 for dissolved silica (dSi) concentrations and stable silicon isotopic compositions. Moreover, to determine the composition and content of bSi, as well as Si sorbed onto metal oxides, we conducted a sequential digestion of surface sediment. Following this we coupled our analyses with reaction transport modelling to further improve our mechanistic understanding of the system and to quantitatively disentangle the relative importance of these diagenetic processes to pore water Si chemistry and benthic fluxes.</p><p>Our work suggests that both interannual and spatial variability of dSi are increased in the southern, AW region of the Barents Sea. Benthic flux estimates for the southern sites have been found to more than double (~30 to 100 mmol m<sup>-2 </sup>yr<sup>-2</sup>) between cruise years, compared to a more consistent flux in the north (~80 mmol m<sup>-2 </sup>yr<sup>-2</sup>). Therefore, future Atlantification of the northern region may enance the variability of dSi supply from the benthos to bottom waters, with potential consequences for diatom productivity in the region.</p>