Net Community Production and Carbon Exchange From Winter to Summer in the Atlantic Water Inflow to the Arctic Ocean

The eastern Fram Strait and area north of Svalbard, are influenced by the inflow of warm Atlantic water, which is high in nutrients and CO2, influencing the carbon flux into the Arctic Ocean. However, these estimates are mainly based on summer data and there is still doubt on the size of the net ocean Arctic CO2 sink. We use data on carbonate chemistry and nutrients from three cruises in 2014 in the CarbonBridge project (January, May, and August) and one in Fram Strait (August). We describe the seasonal variability and the major drivers explaining the inorganic carbon change (CDIC) in the upper 50 m, such as photosynthesis (CBIO), and air-sea CO2 exchange (CEXCH). Remotely sensed data describes the evolution of the bloom and net community production. The focus area encompasses the meltwater-influenced domain (MWD) along the ice edge, the Atlantic water inflow (AWD), and the West Spitsbergen shelf (SD). The CBIO total was 2.2 mol C m–2 in the MWD derived from the nitrate consumption between January and May. Between January and August, the CBIO was 3.0 mol C m–2 in the AWD, thus CBIO between May and August was 0.8 mol C m–2. The ocean in our study area mainly acted as a CO2 sink throughout the period. The mean CO2 sink varied between 0.1 and 2.1 mol C m–2 in the AWD in August. By the end of August, the AWD acted as a CO2 source of 0.7 mol C m–2, attributed to vertical mixing of CO2-rich waters and contribution from respiratory CO2 as net community production declined. The oceanic CO2 uptake (CEXCH) from the atmosphere had an impact on CDIC between 5 and 36%, which is of similar magnitude as the impact of the calcium carbonate (CaCO3, CCALC) dissolution of 6–18%. CCALC was attributed to be caused by a combination of the sea-ice ikaite dissolution and dissolution of advected CaCO3 shells from the south. Indications of denitrification were observed, associated with sea-ice meltwater and bottom shelf processes. CBIO played a major role (48–89%) for the impact on CDIC.publishedVersio

Cold-Water Coral Reefs in the Langenuen Fjord, Southwestern Norway — A Window into Future Environmental Change

Ocean warming and acidification pose serious threats to cold-water corals (CWCs) and the surrounding habitat. Yet, little is known about the role of natural short-term and seasonal environmental variability, which could be pivotal to determine the resilience of CWCs in a changing environment. Here, we provide continuous observational data of the hydrodynamic regime (recorded using two benthic landers) and point measurements of the carbonate and nutrient systems from five Lophelia pertusa reefs in the Langenuen Fjord, southwestern Norway, from 2016 to 2017. In this fjord setting, we found that over a tidal (12 °C) than the mean conditions and high CT concentrations of 20 µmol kg−1 over the suggested threshold for healthy CWC reefs (i.e., >2170 µmol kg−1). Combined with hindcast measurements, our findings indicate that these shallow fjord reefs may act as an early hotspot for ocean warming and acidification. We predict that corals in Langenuen will face seasonally high temperatures (>18 °C) and hypoxic and corrosive conditions within this century. Therefore, these fjord coral communities could forewarn us of the coming consequences of climate change on CWC diversity and function

Long-Term and Seasonal Trends in Estuarine and Coastal Carbonate Systems

Coastal pH and total alkalinity are regulated by a diverse range of local processes superimposed on global trends of warming and ocean acidification, yet few studies have investigated the relative importance of different processes for coastal acidification. We describe long-term (1972-2016) and seasonal trends in the carbonate system of three Danish coastal systems demonstrating that hydrological modification, changes in nutrient inputs from land, and presence/absence of calcifiers can drastically alter carbonate chemistry. Total alkalinity was mainly governed by conservative mixing of freshwater (0.73-5.17mmolkg(-1)) with outer boundary concentrations (similar to 2-2.4mmolkg(-1)), modulated seasonally and spatially (similar to 0.1-0.2mmolkg(-1)) by calcifiers. Nitrate assimilation by primary production, denitrification, and sulfate reduction increased total alkalinity by almost 0.6mmolkg(-1) in the most eutrophic system during a period without calcifiers. Trends in pH ranged from -0.0088year(-1) to 0.021year(-1), the more extreme of these mainly driven by salinity changes in a sluice-controlled lagoon. Temperature increased 0.05 degrees Cyr(-1) across all three systems, which directly accounted for a pH decrease of 0.0008year(-1). Accounting for mixing, salinity, and temperature effects on dissociation and solubility constants, the resulting pH decline (0.0040year(-1)) was about twice the ocean trend, emphasizing the effect of nutrient management on primary production and coastal acidification. Coastal pCO(2) increased similar to 4 times more rapidly than ocean rates, enhancing CO2 emissions to the atmosphere. Indeed, coastal systems undergo more drastic changes than the ocean and coastal acidification trends are substantially enhanced from nutrient reductions to address coastal eutrophication.Peer reviewe

Shell density of planktonic foraminifera and pteropod species Limacina helicina in the Barents Sea: Relation to ontogeny and water chemistry

Planktonic calcifiers, the foraminiferal species Neogloboquadrina pachyderma and Turborotalita quinqueloba, and the thecosome pteropod Limacina helicina from plankton tows and surface sediments from the northern Barents Sea were studied to assess how shell density varies with depth habitat and ontogenetic processes. The shells were measured using X-ray microcomputed tomography (XMCT) scanning and compared to the physical and chemical properties of the water column including the carbonate chemistry and calcium carbonate saturation of calcite and aragonite. Both living L. helicina and N. pachyderma increased in shell density from the surface to 300 m water depth. Turborotalita quinqueloba increased in shell density to 150–200 m water depth. Deeper than 150 m, T. quinqueloba experienced a loss of density due to internal dissolution, possibly related to gametogenesis. The shell density of recently settled (dead) specimens of planktonic foraminifera from surface sediment samples was compared to the living fauna and showed a large range of dissolution states. This dissolution was not apparent from shell-surface texture, especially for N. pachyderma, which tended to be both thicker and denser than T. quinqueloba. Dissolution lowered the shell density while the thickness of the shell remained intact. Limacina helicina also increase in shell size with water depth and thicken the shell apex with growth. This study demonstrates that the living fauna in this specific area from the Barents Sea did not suffer from dissolution effects. Dissolution occurred after death and after settling on the sea floor. The study also shows that biomonitoring is important for the understanding of the natural variability in shell density of calcifying zooplankton.publishedVersio

Hydrography, inorganic nutrients and chlorophyll a linked to sea ice cover in the Atlantic Water inflow region north of Svalbard

Changes in the inflow of Atlantic Water (AW) and its properties to the Arctic Ocean bring more warm water, contribute to sea ice decline, promote borealisation of marine ecosystems, and affect biological and particularly primary productivity in the Eurasian Arctic Ocean. One of the two branches of AW inflow follows the shelf break north of Svalbard, where it dominates oceanographic conditions, bringing in heat, salt, nutrients and organisms. However, the interplay with sea ice and Polar Surface Water (PSW) determines the supply of nutrients to the euphotic layer especially northeast of Svalbard where AW subducts below PSW. In an effort to build up a time series monitoring the key characteristics of the AW inflow, repeat sampling of hydrography, macronutrients (nitrate, phosphate and silicate), and chlorophyll a (chl a) was undertaken along a transect across the AW inflow at 31◦E, 81.5◦N since 2012 — first during late summer and in later years during early winter. Such time series are scarce but invaluable for investigating the range of variability in hydrography and nutrient concentrations. We investigate linkages between late summer hydrographic conditions and nutrient concentrations along the transect and the preceding seasonal dynamics of surface chl a and sea ice cover in the region north of Svalbard. We find large interannual variability in hydrography, nutrients and chl a, indicating varying levels of nutrient drawdown by primary producers over summer. Sea ice conditions varied considerably between the years, impacting upper ocean stratification, light availability and potential wind-driven mixing, with a strong potential for steering chl a concentration over the productive season. Early winter measurements show variable efficiency of nutrient re-supply through vertical mixing when stratification was low, related to autumn wind forcing and sea ice conditions. While this re-supply elevates nutrient levels sufficiently for primary production, it likely happens too late in the season when light levels are already low, limiting the potential for autumn blooms. Such multidisciplinary observations provide insight into the interplay between physical, chemical and biological drivers in the marine environment and are key to understanding ongoing and future changes, especially at this entrance to the central Arctic Ocean

Seasonal dynamics of the marine CO2 system in Adventfjorden, a West Spitsbergen fjord

Time series of the marine CO2 system and related parameters at the IsA Station, by Adventfjorden, Svalbard, were investigated between March 2015 and November 2017. The physical and biogeochemical processes that govern changes in total alkalinity (TA), total dissolved inorganic carbon (DIC) and the saturation state of the calcium carbonate mineral aragonite (ΩAr) were assessed on a monthly timescale. The major driver for TA and DIC was changes in salinity, caused by river runoff, mixing and advection. This accounted for 77 and 45%, respectively, of the overall variability. It contributed minimally to the variability in ΩAr (5%); instead, biological activity was responsible for 60% of the monthly variations. For DIC, the biological activity was also important, contributing 44%. The monthly effect of air–sea CO2 fluxes accounted for 11 and 15% of the total changes in DIC and ΩAr, respectively. Net community production (NCP) during the productive season ranged between 65 and 85 g C m−2, depending on the year and the presence of either Arctic water or transformed Atlantic water (TAW). The annual NCP as estimated from DIC consumption was 34 g C m−2 yr−1 in 2016, which was opposite in direction but similar in magnitude to the integrated annual air–sea CO2 flux (i.e., uptake of carbon from the atmosphere) of −29 g C m−2 yr−1 for the same year. The results showed that increased intrusions of TAW into Adventfjorden in the future could possibly lower the NCP, with the potential to reduce the CO2buffer capacity and ΩAr over the summer season.publishedVersio

Methane release from open leads and new ice following an Arctic winter storm event

We examine an Arctic winter storm event, which led to ice break–up, the formation of open leads, and the subsequent freezing of these leads. The methane (CH4) concentration in under–ice surface water before and during the storm event was 8–12 nmol L−1, which resulted in a potential sea–to–air CH4 flux ranging from +0.2 to +2.1 mg CH4 m−2 d−1 in open leads. CH4 ventilation between seawater and atmosphere occurred when both open water fraction and wind speed increased. Over the nine days after the storm, sea ice grew 27 cm thick. Initially, CH4 concentrations in the sea ice brine were above the equilibrium with the atmosphere. As the ice grew thicker, most of the CH4 was lost from upper layers of sea ice into the atmosphere, implying continued CH4 evasion after the leads were ice–covered. This suggests that wintertime CH4 emissions need to be better constrained

Ocean acidification state variability of the Atlantic Arctic Ocean around northern Svalbard

The Svalbard shelf and Atlantic Arctic Ocean are a transition zone between northward flowing Atlantic Water and ice-covered waters of the Arctic. Effects of regional ocean warming, sea ice loss and greater influence of Atlantic Water or “Atlantification” on the state of ocean acidification, i.e. calcium carbonate (CaCO3) saturation (Ω) are yet to be fully understood. Anomalies in surface layer Ω for the climatically-vulnerable CaCO3 mineral aragonite (ΔΩ) were determined by considering the variability in Ωaragonite during late summer each year from 2014 to 2017 relative to the four-year average. Greatest sea ice extent and more Arctic-like conditions in 2014 resulted in ΔΩ anomalies of −0.05 to −0.01 (up to 45% of total ΔΩ) as a result of lower primary production. Conversely, greater Atlantic Water influence in 2015 supplied the ice-free surface layer with nitrate, which prolonged primary production to drive ΔΩ anomalies of 0.01 to 0.06 (up to 45% of total ΔΩ) in more Atlantic-like conditions. Additionally, dissolution of CaCO3 increased carbonate ion concentrations giving ΔΩ anomalies up to 0.06 (up to 52% of total ΔΩ). These processes enhanced surface water Ω, which ranged between 2.01 and 2.65 across the region. Recent sea ice retreat in 2016 and 2017 (rate of decrease in ice cover of ∼4% in 30 days) created transitional Atlantic-Arctic conditions, where surface water Ω varied between 1.87 and 2.29 driven by ΔΩ anomalies of −0.10 to 0.01 due to meltwater inputs and influence of Arctic waters. Anomalies as low as −0.12 from reduced CaCO3 dissolution in 2016 further supressed Ω. Wind-driven mixing in 2017 entrained Atlantic Water with low Ω into the surface layer to drive large ΔΩ anomalies of −0.15 (up to 58% of ΔΩ). Sea-ice meltwater provided a minor source of carbonate ions, slightly counteracting dilution effects. Ice-free surface waters were substantial sinks for atmospheric CO2, where uptake of 20.5 mmol m−2 day−1 lowered surface water Ω. “Atlantification” could exacerbate or alleviate acidification of the Arctic Ocean, being highly dependent on the numerous factors examined here that are intricately linked to the sea ice-ocean system variability.publishedVersio

Methane release from open leads and new ice following an Arctic winter storm event

We examine an Arctic winter storm event, which led to ice break–up, the formation of open leads, and the subsequent freezing of these leads. The methane (CH4) concentration in under–ice surface water before and during the storm event was 8–12 nmol L−1, which resulted in a potential sea–to–air CH4 flux ranging from +0.2 to +2.1 mg CH4 m−2 d−1 in open leads. CH4 ventilation between seawater and atmosphere occurred when both open water fraction and wind speed increased. Over the nine days after the storm, sea ice grew 27 cm thick. Initially, CH4 concentrations in the sea ice brine were above the equilibrium with the atmosphere. As the ice grew thicker, most of the CH4 was lost from upper layers of sea ice into the atmosphere, implying continued CH4 evasion after the leads were ice–covered. This suggests that wintertime CH4 emissions need to be better constrainedMethane release from open leads and new ice following an Arctic winter storm eventacceptedVersio

Antarctic sea ice carbon dioxide system and controls

In austral summer, from December 2008 to January 2009, we investigated the sea-ice carbon dioxide (CO(2)) system and CO(2) controls in the Amundsen and Ross Seas, Antarctica. We sampled seawater, brine and sea ice for the measurements of total alkalinity (A(T)), total inorganic carbon (DIC), pH, inorganic nutrients, particulate organic carbon (POC) and nitrogen (PON), chlorophyll a, pigments, salinity and temperature. Large variability in all measured parameters was observed in time and space due to the complex sea-ice dynamics. We discuss the controls of the sea-ice CO(2) system, such as brine rejection, biological processes, calcium carbonate (CaCO(3)) precipitation/dissolution and CO(2) exchange. Most (80 to 90%) of the DIC loss was due to brine rejection, which suggests that the sea ice acted as an efficient DIC sink from 0.8 and 2.6 mol m(-2) yr(-1) (9.6-31 g C m(-2) yr(-1)). The remaining change in DIC was to a large extent explained by net biological production. The A(T):DIC ratio in the sea ice was higher than in the under-ice water (UIW), with ratios reaching 1.7, which indicated CaCO(3) precipitation and concomitant DIC loss in the sea ice. Elevated A(T):DIC ratios and carbonate concentrations were also observed in the UIW, which reflect the solid CaCO(3) rejected from the ice during melt. The potential for uptake of atmospheric CO(2) in the mixed layer increased by approximately 56 mu atm due to the combined effect of CaCO(3) precipitation during ice formation, and ice melt in summer