Description: Silica is an essential element for marine life and plays a key role in the biogeochemistry of the ocean. Glacial activity stimulates rock weathering, generating dissolved silica that is exported to coastal areas along with meltwater. The magnitude of the dissolved silica export from large glacial areas such as the Greenland Ice Sheet is presently poorly quantified and not accounted for in global budgets. Here we present data from two fjord systems adjacent to the Greenland Ice Sheet which reveal a large export of dissolved silica by glacial meltwater relative to other macronutrients. Upscaled to the entire Greenland Ice Sheet, the export of dissolved silica equals 22 ± 10 Gmol Si yr−1. When the silicate-rich meltwater mixes with upwelled deep water, either inside or outside Greenland's fjords, primary production takes place at increased silicate to nitrate ratios. This likely stimulates the growth of diatoms relative to other phytoplankton groups.

Description: Key Points In Kongsfjorden, an Arctic glacier fjord, freshwater from glacier runoff and ice meltwater decreases phosphate, alkalinity and DOM concentrations Estuarine mixing is the major driver of summer CO2 undersaturation in glacially modified waters and near‐corrosive conditions were observed Future changes will amplify ocean acidification in the inner‐fjord surface waters Abstract A detailed survey of a high Arctic glacier fjord (Kongsfjorden, Svalbard) was carried out in summer 2016, close to the peak of the meltwater season, in order to identify the effects of glacier runoff on nutrient distributions and the carbonate system. Short‐term weather patterns were found to exert a strong influence on freshwater content within the fjord. Freshwater inputs from glacier runoff and ice meltwater averaged (±SD) low nitrate (1.85±0.47 μM; 0.41±0.99 μM), orthophosphate (0.07±0.27 μM; 0.02 ±0.03 μM), dissolved organic carbon (27 ±14 μM in glacier runoff), total alkalinity (708±251 μmol kg‐1; 173±121 μmol kg‐1) and dissolved inorganic carbon (622±108 μmol kg‐1; 41±88 μmol kg‐1), as well as a modest silicate concentration (3.71±0.02 μM; 3.16±5.41 μM). pCO2 showed a non‐conservative behavior across the estuarine salinity gradient with a pronounced under‐saturation in the inner‐fjord, leading to strong CO2 uptake from the atmosphere. The combined effect of freshwater dilution and atmospheric CO2 absorption was the lowering of aragonite saturation state, to values that are known to negatively affect marine calcifiers (ΩAr, 1.07). Glacier discharge was therefore a strong local amplifier of ocean acidification. Future increases in discharge volume and the loss of marine productivity following the retreat of marine‐terminating glaciers inland are both anticipated to further lower ΩAr within inner‐fjord surface waters. This shift may be partially buffered by an increase in the mean freshwater total alkalinity as the fractional importance of iceberg melt to freshwater fjord inputs declines and runoff increases.

Description: The duration and magnitude of the North Atlantic spring bloom impacts both higher trophic levels and oceanic carbon sequestration. Nutrient exhaustion offers a general explanation for bloom termination, but detail on which nutrients and their relative influence on phytoplankton productivity, community structure, and physiology is lacking. Here, we address this using nutrient addition bioassay experiments conducted across the midlatitude North Atlantic in June 2017 (late spring). In four out of six experiments, phytoplankton accumulated over 48–72 h following individual additions of either iron (Fe) or nitrogen (N). In the remaining two experiments, Fe and N were serially limiting, that is, their combined addition sequentially enhanced phytoplankton accumulation. Silicic acid (Si) added in combination with N + Fe led to further chlorophyll a (Chl a) enhancement at two sites. Conversely, addition of zinc, manganese, cobalt, vitamin B12, or phosphate in combination with N + Fe did not. At two sites, the simultaneous supply of all six nutrients, in combination with N + Fe, also led to no further Chl a enhancement, but did result in an additional 30–60% particulate carbon accumulation. This particulate carbon accumulation was not matched by a Redfield equivalent of particulate N, characteristic of high C:N organic exudates that enhance cell aggregation and sinking. Our results suggest that growth rates of larger phytoplankton were primarily limited by Fe and/or N, making the availability of these nutrients the main bottom‐up factors contributing to spring bloom termination. In addition, the simultaneous availability of other nutrients could modify bloom characteristics and carbon export efficiency.

Description: Marine nitrogen (N2) fixation supports significant primary productivity in the global ocean. However, in one of the most productive regions of the world ocean, the northern Humboldt Upwelling System (HUS), the magnitude and spatial distribution of this process remains poorly characterized. This study presents a spatially resolved dataset of N2 fixation rates across six coastal transects of the northern HUS off Peru (8°S – 16°S) during austral summer. N2 fixation rates were detected throughout the waters column including within the OMZ between 12°S and 16°S. N2 fixation rates were highest where the subsurface Oxygen Minimum Zone (OMZ, O2 〈20 µmol L-1) was most intense and estimated nitrogen (N) loss was highest. There, rates were measured throughout the water column. Hence the vertical and spatial distribution of rates indicates colocation of N2 fixation with N loss in the coastal productive waters of the northern HUS. Despite high phosphate and total dissolvable iron (TdFe) concentrations throughout the study area, N2 fixation was still generally low (1.19 ± 3.81 nmol L-1 d-1) and its distribution could not be directly explained by these two factors. Our results suggest that the distribution was likely influenced by a complex interplay of environmental factors including phytoplankton biomass and organic matter availability, and potentially iron, or other trace metal (co)-limitation of both N2 fixation and primary production. In general, our results support previous conclusions that N2 fixation in the northern HUS plays a minor role as a source of new N and to replenish the regional N loss. Key Points: A north-to-south pattern in N2 fixation rates was observed implying increased N turnover between 12°S and 16°S where N loss was pronounced Highest N2 fixation rates were measured in coastal productive waters above and within the OMZ, showing no clear relationship with Fe or P The magnitude of N2 fixation was low compared to predictions, estimated to account for ∼0.3% of primary production and 〈2% of local N loss

Description: Key Points: - Glacier-derived particles release 2–46% of labile particulate lead (Pb) upon mixing with seawater - Pb dynamics in glacier fjords are characterized by a rapid release of dissolved Pb followed by readsorption on a timescale of hours-to-days - Dissolved Pb release from the Greenland Ice Sheet is likely within the range 0.2–1 Mmol yr−1 Higher than expected concentrations of dissolved lead (dPb) have been consistently observed along glaciated coastlines and it is widely hypothesized that there is a net release of dPb from glacier-derived sediments. Here we further corroborate that dPb concentrations in diverse locations around west Greenland (3.2–252 pM) and the Western Antarctic Peninsula (7.7–107 pM) appear to be generally higher than can be explained by addition of dPb from glacier-derived freshwater. The distribution of dPb across the salinity gradient is unlike any other commonly studied trace element (e.g., Fe, Co, Ni, Cu, Mn, and Al) implying a dynamic, reversible exchange between dissolved and labile particulate Pb. Incubating a selection of glacier-derived particles from SW Greenland (Ameralik and Nuup Kangerlua) and Svalbard (Kongsfjorden), with a range of labile particulate Pb (LpPb) content (11–113 nmol g−1), the equivalent of 2–46% LpPb was released as dPb within 24 hr of addition to Atlantic seawater. Over longer time periods, the majority of this dPb was typically readsorbed. Sediment loading was the dominant factor influencing the net release of dPb into seawater, with a pronounced decline in net dPb release efficiency when sediment load increased from 20 to 500 mg L−1. Yet temperature also had some effect with 68 ± 22% higher dPb release at 11°C compared to 4°C. Future regional changes in dPb dynamics may therefore be more sensitive to short-term suspended sediment dynamics, and potentially temperature changes, than to changing interannual runoff volume.

Description: The Arctic Ocean is considered a source of micronutrients to the Nordic Seas and the North Atlantic Ocean through the gateway of Fram Strait. However, there is a paucity of trace element data from across the Arctic Ocean gateways, and so it remains unclear how Arctic and North Atlantic exchange shapes micronutrient availability in the two ocean basins. In 2015 and 2016, GEOTRACES cruises sampled the Barents Sea Opening (GN04, 2015) and Fram Strait (GN05, 2016) for dissolved iron (dFe), manganese (dMn), cobalt (dCo), nickel (dNi), copper (dCu) and zinc (dZn). Together with the most recent synopsis of Arctic-Atlantic volume fluxes, the observed trace element distributions suggest that Fram Strait is the most important gateway for Arctic-Atlantic dissolved micronutrient exchange as a consequence of Intermediate and Deep Water transport. Combining fluxes from Fram Strait and the Barents Sea Opening with estimates for Davis Strait (GN02, 2015) suggests an annual net southward flux of 2.7 ± 2.4 Gg·a-1 dFe, 0.3 ± 0.3 Gg·a-1 dCo, 15.0 ± 12.5 Gg·a-1 dNi and 14.2 ± 6.9 Gg·a-1 dCu from the Arctic towards the North Atlantic Ocean. Arctic-Atlantic exchange of dMn and dZn were more balanced, with a net southbound flux of 2.8 ± 4.7 Gg·a-1 dMn and a net northbound flux of 3.0 ± 7.3 Gg·a-1 dZn. Our results suggest that ongoing changes to shelf inputs and sea ice dynamics in the Arctic, especially in Siberian shelf regions, affect micronutrient availability in Fram Strait and the high latitude North Atlantic Ocean.

Description: Cyclonic ocean eddies drive upwelling of deep waters enhanced in nutrients, which can elevate phytoplankton productivity. At mid‐latitudes in the North Atlantic, satellite images show enhanced chlorophyll‐a associated with eddies. However, surface macronutrient concentrations are often not fully depleted in this region, implying enhanced macronutrient supply is not the primary control. We conducted high resolution sampling through two mid‐latitude Atlantic eddies in late spring, located 800 and 350 km east of the Newfoundland Grand Banks. Waters outside of both eddies had unused residual macronutrients, low dissolved iron, and iron‐stressed phytoplankton. Inside both eddies, plankton biomass was higher and macronutrient concentrations lower. However, full macronutrient drawdown and an absence of iron stress were only present in the eddy nearer the continental shelf. From these two examples, iron supply and proximity to shelf iron sources appear to be important factors regulating productivity and macronutrient utilization in mid‐latitude North Atlantic cyclonic eddies.

Description: We present high-resolution profiles of dissolved, labile and total particulate trace metals (TMs) on the Northeast Greenland shelf from GEOTRACES cruise GN05 in August 2016. Combined with radium isotopes, stable oxygen isotopes, and noble gas measurements, elemental distributions suggest that TM dynamics were mainly regulated by the mixing between North Atlantic-derived Intermediate Water, enriched in labile particulate TMs (LpTMs), and Arctic surface waters, enriched in Siberian shelf-derived dissolved TMs (dTMs; Co, Cu, Fe, Mn, and Ni) carried by the Transpolar Drift. These two distinct sources were delineated by salinity-dependent variations of dTM and LpTM concentrations and the proportion of dTMs relative to the total dissolved and labile particulate ratios. Locally produced meltwater from the Nioghalvfjerdsbræ (79NG) glacier cavity, distinguished from other freshwater sources using helium excess, contributed a large pool of dTMs to the shelf inventory. Localized peaks in labile and total particulate Cd, Co, Fe, Mn, Ni, Cu, Al, V, and Ti in the cavity outflow, however, were not directly contributed by submarine melting. Instead, these particulate TMs were mainly supplied by the re-suspension of cavity sediment particles. Currently, Arctic Ocean outflows are the most important source of dFe, dCu and dNi on the shelf, while LpTMs and up to 60% of dMn and dCo are mainly supplied by subglacial discharge from the 79NG cavity. Therefore, changes in the cavity-overturning dynamics of 79NG induced by glacial retreat, and alterations in the transport of Siberian shelf-derived materials with the Transport Drift may shift the shelf dTM-LpTM stoichiometry in the future. Key Points The overall dissolved and particulate trace metal dynamics were mainly regulated by the mixing with Arctic surface waters Resuspension of cavity sediments is a major localized source of labile and total particulate Cd, Co, Fe, Mn, Ni, Cu, Al, V, and Ti Whilst dissolved and particulate trace metals are mostly coupled on the Greenland shelf, cavity outflow decouples both phases

Description: Concentrations of the toxic element lead (Pb) are elevated in seawater due to historical emissions. While anthropogenic atmospheric emissions are the dominant source of dissolved Pb (dPb) to the Atlantic Ocean, evidence is emerging of a natural source associated with subglacial discharge into the ocean but this has yet to be constrained around Greenland. Here, we show subglacial discharge from the cavity underneath Nioghalvfjerdsbræ floating ice tongue, is a previously unrecognized source of dPb to the NE Greenland Shelf. Contrasting cavity-inflowing and cavity-outflowing waters, we constrain the associated net-dPb flux as 2.2 ± 1.4 Mg·yr−1, of which ∼90% originates from dissolution of glacial bedrock and cavity sediments. We propose that the retreat of the floating ice tongue, the ongoing retreat of many glaciers on Greenland, associated shifts in sediment dynamics, and enhanced meltwater discharges into shelf waters may result in pronounced changes, possibly increases, in net-dPb fluxes to coastal waters. Key Points - Helium and neon show strong evidence for a subglacial source of Pb discharging onto the NE Greenland Shelf - Contrasting inflowing and outflowing waters beneath the floating ice tongue of Nioghalvfjerdsbræ shows a 2-3-fold dPb enrichment - The dissolved Pb flux from Nioghalvfjerdsbræ (2.2 ± 1.4 Mg·yr−1) is comparable to small Arctic rivers, with ∼90% of a sedimentary origin

Description: An insufficient supply of the micronutrient iron (Fe) limits phytoplankton growth across large parts of the ocean. Ambient Fe speciation and solubility are largely dependent on seawater physico-chemical properties. We calculated the apparent Fe solubility (SFe(III)app) at equilibrium for ambient conditions, where SFe(III)app is defined as the sum of aqueous inorganic Fe(III) species and Fe(III) bound to organic matter formed at a free Fe3+ concentration equal to the solubility of Fe hydroxide. We compared the SFe(III)app to measured dissolved Fe (dFe) in the Atlantic and Pacific Oceans. The SFe(III)app was overall ∼2 to 4-fold higher than observed dFe at depths less than 1000 m, ∼2-fold higher than the dFe between 1000-4000 m and ∼3-fold higher than dFe below 4000 m. Within the range of used parameters, our results showed that there was a similar trend in the vertical distributions of horizontally averaged SFe(III)app and dFe. Our results suggest that vertical dFe distributions are underpinned by changes in SFe(III)app which are driven by relative changes in ambient pH and temperature. Since both pH and temperature are essential parameters controlling ambient Fe speciation, these should be accounted for in investigations of changing Fe dynamics, particularly in the context of ocean acidification and warming. Key Points Apparent iron solubility is driven by ambient pH, temperature (T) and dissolved organic carbon (DOC), and showed a 6-fold variation between surface (pH= 8.05 on the total scale, DOC= 71.8 µmol L-1, T= 20.4 °C) and deep oceanic waters (pH= 7.82, DOC= 38.6 µmol L-1, T= 1.1°C). Higher values of apparent iron solubility were determined for deep Atlantic and Pacific waters, with lower values in subtropical gyres. Calculated apparent iron solubility showed a similar trend in vertical distribution to dissolved iron, highlighting the importance of considering the impact of changes in ambient physico-chemical conditions on seawater iron chemistry.