Storm-induced water dynamics and thermohaline structure at the tidewater Flade Isblink Glacier outlet to theWandel Sea (NE Greenland)

In April 2015, an ice-tethered conductivity&ndash;temperature&ndash;depth (CTD) profiler and a down-looking acoustic Doppler current profiler (ADCP) were deployed from the landfast ice near the tidewater glacier terminus of the Flade Isblink Glacier in the Wandel Sea, NE Greenland. The 3-week time series showed that water dynamics and the thermohaline structure were modified considerably during a storm event on 22&ndash;24 April, when northerly winds exceeded 15 m s⁻¹. The storm initiated downwelling-like water dynamics characterized by on-shore water transport in the surface (0&ndash;40 m) layer and compensating offshore flow at intermediate depths. After the storm, currents reversed in both layers, and the relaxation phase of downwelling lasted ∼&thinsp;4 days. Although current velocities did not exceed 5 cm s⁻¹, the enhanced circulation during the storm caused cold turbid intrusions at 75&ndash;95 m depth, which are likely attributable to subglacial water from the Flade Isblink Ice Cap. It was also found that the semidiurnal periodicities in the temperature and salinity time series were associated with the lunar semidiurnal tidal flow. The vertical structure of tidal currents corresponded to the first baroclinic mode of the internal tide with a velocity minimum at ∼&thinsp;40 m. The tidal ellipses rotate in opposite directions above and below this depth and cause a divergence of tidal flow, which was observed to induce semidiurnal internal waves of about 3 m height at the front of the glacier terminus. <br><br> Our findings provide evidence that shelf&ndash;basin interaction and tidal forcing can potentially modify coastal Wandel Sea waters even though they are isolated from the atmosphere by landfast sea ice almost year-round. The northerly storms over the continental slope cause an enhanced circulation facilitating a release of cold and turbid subglacial water to the shelf. The tidal flow may contribute to the removal of such water from the glacial terminus

Estimates of ikaite export from sea ice to the underlying seawater in a sea ice-seawater mesocosm

The precipitation of ikaite and its fate within sea ice is still poorly understood.We quantify temporal inorganic carbon dynamics in sea ice from initial formation to its melt in a sea ice.seawater mesocosm pool from 11 to 29 January 2013. Based on measurements of total alkalinity (TA) and total dissolved inorganic carbon (TCO2), the main processes affecting inorganic carbon dynamics within sea ice were ikaite precipitation and CO2 exchange with the atmosphere. In the underlying seawater, the dissolution of ikaite was the main process affecting inorganic carbon dynamics. Sea ice acted as an active layer, releasing CO2 to the atmosphere during the growth phase, taking up CO2 as it melted and exporting both ikaite and TCO2 into the underlying seawater during the whole experiment. Ikaite precipitation of up to 167 μmolkg-1 within sea ice was estimated, while its export and dissolution into the underlying seawater was responsible for a TA increase of 64.66 μmolkg-1 in the water column. The export of TCO2 from sea ice to the water column increased the underlying seawater TCO2 by 43.5 μmolkg-1, suggesting that almost all of the TCO2 that left the sea ice was exported to the underlying seawater. The export of ikaite from the ice to the underlying seawater was associated with brine rejection during sea ice growth, increased vertical connectivity in sea ice due to the upward percolation of seawater and meltwater flushing during sea ice melt. Based on the change in TA in the water column around the onset of sea ice melt, more than half of the total ikaite precipitated in the ice during sea ice growth was still contained in the ice when the sea ice began to melt. Ikaite crystal dissolution in the water column kept the seawater pCO2 undersaturated with respect to the atmosphere in spite of increased salinity, TA and TCO2 associated with sea ice growth. Results indicate that ikaite export from sea ice and its dissolution in the underlying seawater can potentially hamper the effect of oceanic acidification on the aragonite saturation state (ωaragonite) in fall and in winter in ice-covered areas, at the time when ωaragonite is smallest

Spring bloom dynamics in a subarctic fjord influenced by tidewater outlet glaciers (Godthåbsfjord, SW Greenland)

In high-latitude fjord ecosystems, the spring bloom accounts for a major part of the annual primary production and thus provides a crucial energy supply to the marine food web. However, the environmental factors that control the timing and intensity of these spring blooms remain uncertain. In 2013, we studied the spring bloom dynamics in Godthåbsfjord, a large fjord system adjacent to the Greenland Ice Sheet. Our surveys revealed that the spring bloom did not initiate in the inner stratified part of the fjord system but only started farther away from tidewater outlet glaciers. A combination of out-fjord winds and coastal inflows drove an upwelling in the inner part of the fjord during spring (April–May), which supplied nutrient-rich water to the surface layer. This surface water was subsequently transported out-fjord, and due to this circulation regime, the biomass accumulation of phytoplankton was displaced away from the glaciers. In late May, the upwelling weakened and the dominant wind direction changed, thus reversing the direction of the surface water transport. Warmer water was now transported toward the inner fjord, and a bloom was observed close to the glacier terminus. Overall, our findings imply that the timing, intensity, and location of the spring blooms in Godthåbsfjord are controlled by a combination of upwelling strength and wind forcing. Together with sea ice cover, the hydrodynamic regime hence plays a crucial role in structuring food web dynamics of the fjord ecosystem

Oxygen exchange and ice melt measured at the ice-water interface by eddy correlation

This study examined fluxes across the ice-water interface utilizing the eddy correlation technique. Temperature eddy correlation systems were used to determine rates of ice melting and freezing, and O&lt;sub&gt;2&lt;/sub&gt; eddy correlation systems were used to examine O&lt;sub&gt;2&lt;/sub&gt; exchange rates driven by biological and physical processes. The study was conducted below 0.7 m thick sea-ice in mid-March 2010 in a southwest Greenland fjord and revealed low rates of ice melt at a maximum of 0.80 mm d&lt;sup&gt;−1&lt;/sup&gt;. The O&lt;sub&gt;2&lt;/sub&gt; flux associated with release of O&lt;sub&gt;2&lt;/sub&gt; depleted melt water was less than 13 % of the average daily O&lt;sub&gt;2&lt;/sub&gt; respiration rate. Ice melt and insufficient vertical turbulent mixing due to low current velocities caused periodic stratification immediately below the ice. This prevented the determination of fluxes 61 % of the deployment time. These time intervals were identified by examining the velocity and the linearity and stability of the cumulative flux. The examination of unstratified conditions through vertical velocity and O&lt;sub&gt;2&lt;/sub&gt; spectra and their cospectra revealed characteristic fingerprints of well-developed turbulence. From the measured O&lt;sub&gt;2&lt;/sub&gt; fluxes a photosynthesis/irradiance curve was established by least-squares fitting. This relation showed that light limitation of net photosynthesis began at 4.2 μmol photons m&lt;sup&gt;−2&lt;/sup&gt; s&lt;sup&gt;−1&lt;/sup&gt;, and that algal communities were well-adapted to low-light conditions as they were light saturated for 75 % of the day during this early spring period. However, the sea-ice associated microbial and algal community was net heterotrophic with a daily gross primary production of 0.69 mmol O&lt;sub&gt;2&lt;/sub&gt; m&lt;sup&gt;−2&lt;/sup&gt; d&lt;sup&gt;−1&lt;/sup&gt; and a respiration rate of −2.13 mmol O&lt;sub&gt;2&lt;/sub&gt; m&lt;sup&gt;−2&lt;/sup&gt; d&lt;sup&gt;−1&lt;/sup&gt; leading to a net ecosystem metabolism of −1.45 mmol O&lt;sub&gt;2&lt;/sub&gt; m&lt;sup&gt;−2&lt;/sup&gt; d&lt;sup&gt;−1&lt;/sup&gt;. This application of the eddy correlation technique produced high temporal resolution O&lt;sub&gt;2&lt;/sub&gt; fluxes and ice melt rates that were measured without disturbing the in situ environmental conditions while integrating over an area of approximately 50 m&lt;sup&gt;2&lt;/sup&gt; which incorporated the highly variable activity and spatial distributions of sea-ice communities

Seasonal carbon cycling in a Greenlandic fjord: an integrated pelagic and benthic study

Climate change is expected to have a pronounced effect on biogeochemical cycling in Arctic fjords, but current insight on the biogeochemical functioning of these systems is limited. Here, we present seasonal data on primary production, export of particulate organic carbon (POC), and the coupling to benthic biogeochemistry in Kobbefjord (SW Greenland). Primary production and associated POC export from the photic zone showed marked seasonality, with annual integrated values of 7.2 and 19.9 mol C m-2 yr-1, respectively. This discrepancy, the isotopic signature, and C:N ratio of the sedimentating material suggested substantial import of marine POC from outside the fjord. At least 52% of the POC export reached the sediment, but the seasonality in pelagic productivity was not reflected in the sediment biogeochemistry, showing only moderate variation. Benthic mineralization and burial of organic carbon amounted to 3.2 and 5.3 mol C m-2 yr-1, respectively. Sulfate reduction was the most prominent mineralization pathway, accounting for 69% of the benthic mineralization, while denitrification accounted for 2%. Overall, the carbon mineralization and burial in Kobbefjord were significantly higher than previously observed in other more northerly Arctic fjords. Data compilation from Arctic fjords suggests proportional increases in surface production, POC export, benthic mineralization and burial of organic material with increasing duration of the ice-free period. Thus, the projected decline in ice coverage in higher Arctic Greenlandic fjords will, as a first approximation, entail proportional increases in productivity, mineralization, and burial of organic carbon in the fjords, which will thus become similar to present-day southerly systems

Sea ice contribution to the air–sea CO₂ exchange in the Arctic and Southern Oceans

Although salt rejection from sea ice is a key process in deep-water formation in ice-covered seas, the concurrent rejection of CO2 and the subsequent effect on air–sea CO2 exchange have received little attention. We review the mechanisms by which sea ice directly and indirectly controls the air–sea CO2 exchange and use recent measurements of inorganic carbon compounds in bulk sea ice to estimate that oceanic CO2 uptake during the seasonal cycle of sea-ice growth and decay in ice-covered oceanic regions equals almost half of the net atmospheric CO2 uptake in ice-free polar seas. This sea-ice driven CO2 uptake has not been considered so far in estimates of global oceanic CO2 uptake. Net CO2 uptake in sea-ice–covered oceans can be driven by; (1) rejection during sea–ice formation and sinking of CO2-rich brine into intermediate and abyssal oceanic water masses, (2) blocking of air–sea CO2 exchange during winter, and (3) release of CO2-depleted melt water with excess total alkalinity during sea-ice decay and (4) biological CO2 drawdown during primary production in sea ice and surface oceanic waters

Sea ice <i>p</i>CO₂ dynamics and air-ice CO₂ fluxes during the Sea Ice Mass Balance in the Antarctic (SIMBA) experiment - Bellingshausen Sea, Antarctica

Temporal evolution of pCO2 profiles in sea ice in the Bellingshausen Sea, Antarctica, in October 2007 shows physical and thermodynamic processes controls the CO2 system in the ice. During the survey, cyclical warming and cooling strongly influenced the physical, chemical, and thermodynamic properties of the ice cover. Two sampling sites with contrasting characteristics of ice and snow thickness were sampled: one had little snow accumulation (from 8 to 25 cm) and larger temperature and salinity variations than the second site, where the snow cover was up to 38 cm thick and therefore better insulated the underlying sea ice. We show that each cooling/warming event was associated with an increase/decrease in the brine salinity, total alkalinity (TA), total dissolved inorganic carbon (TCO2), and in situ brine and bulk ice CO2 partial pressures (pCO2). Thicker snow covers reduced the amplitude of these changes: snow cover influences the sea ice carbonate system by modulating the temperature and therefore the salinity of the sea ice cover. Results indicate that pCO2 was undersaturated with respect to the atmosphere both in the in situ bulk ice (from 10 to 193 µatm) and brine (from 65 to 293 µatm), causing the sea ice to act as a sink for atmospheric CO2 (up to 2.9 mmol m-2 d-1), despite supersaturation of the underlying seawater (up to 462 µatm)

Inorganic carbon dynamics of melt-pond-covered first-year sea ice in the Canadian Arctic

Melt pond formation is a common feature of spring and summer Arctic sea ice, but the role and impact of sea ice melt and pond formation on both the direction and size of CO2 fluxes between air and sea is still unknown. Here we report on the CO2-carbonate chemistry of melting sea ice, melt ponds and the underlying seawater as well as CO2 fluxes at the surface of first-year landfast sea ice in the Resolute Passage, Nunavut, in June 2012. Early in the melt season, the increase in ice temperature and the subsequent decrease in bulk ice salinity promote a strong decrease of the total alkalinity (TA), total dissolved inorganic carbon (T CO2) and partial pressure of CO2 (pCO2) within the bulk sea ice and the brine. As sea ice melt progresses, melt ponds form, mainly from melted snow, leading to a low in situ melt pond pCO2 (36 μatm). The percolation of this low salinity and low pCO2 meltwater into the sea ice matrix decreased the brine salinity, TA and T CO2, and lowered the in situ brine pCO2 (to 20 μatm). This initial low in situ pCO2 observed in brine and melt ponds results in air-ice CO2 fluxes ranging between -0.04 and -5.4 mmolm-2 day-1 (negative sign for fluxes from the atmosphere into the ocean). As melt ponds strive to reach pCO2 equilibrium with the atmosphere, their in situ pCO2 increases (up to 380 μatm) with time and the percolation of this relatively high concentration pCO2 meltwater increases the in situ brine pCO2 within the sea ice matrix as the melt season progresses. As the melt pond pCO2 increases, the uptake of atmospheric CO2 becomes less significant. However, since melt ponds are continuously supplied by meltwater, their in situ pCO2 remains undersaturated with respect to the atmosphere, promoting a continuous but moderate uptake of CO2 (∼-1 mmolm-2 day-1) into the ocean. Considering the Arctic seasonal sea ice extent during the melt period (90 days), we estimate an uptake of atmospheric CO2 of -10.4 Tg of Cyr-1. This represents an additional uptake of CO2 associated with Arctic sea ice that needs to be further explored and considered in the estimation of the Arctic Ocean's overall CO2 budget

Replacement of multiyear sea ice and changes in the open water season duration in the Beaufort Sea since 2004

The last decade has witnessed the nine lowest Arctic September sea ice extents in the observational record. It also forms the most recent third of the long-term trend in that record, which reached -13.4% decade-1 in 2015. While hemispheric analyses paint a compelling picture of sea ice loss across the Arctic, the situation with multiyear ice in the Beaufort Sea is particularly dire. This study was undertaken in light of substantial changes that have occurred in the extent of summer multiyear sea ice in the Arctic inferred from the passive microwave record. To better elucidate these changes at a sub-regional scale, we use data from the Canadian Ice Service archive, the most direct observations of sea ice stage-of-development available. We also build upon the only previous sea ice climatological analysis for Canada's western Arctic region by sea ice stage-of-development that ended in 2004. The annual evolution of sea ice by stage of development in Canada's western Arctic changed dramatically between 1983 and 2014. The rate of these changes and their spatial prevalence were most prominent in the last decade. In summer, total sea ice loss occurred via reductions in old and first-year sea ice over increasingly large areas and over more months per year. Resultant delay of thermodynamic freeze up has increased the annual open water duration in the study region. The winter sea ice cover was increasingly composed of first-year sea ice at the expense of old ice. Breakup timing has not significantly changed in the region

High export of dissolved silica from the Greenland Ice Sheet

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