ALBERT

Description: We suggest the application of a flux parameterization commonly used over terrestrial areas for calculation of CO2 fluxes over sea ice surfaces. The parameterization is based on resistance analogy. We present a concept for parameterization of the CO2 fluxes over sea ice suggesting to use properties of the atmosphere and sea ice surface that can be measured or calculated on a routine basis. Parameters, which can be used in the conceptual model, are analysed based on data sampled from a seasonal fast-ice area, and the different variables influencing the exchange of CO2 between the atmosphere and ice are discussed. We found the flux to be small during the late winter with fluxes in both directions. Not surprisingly we find that the resistance across the surface controls the fluxes and detailed knowledge of the brine volume and carbon chemistry within the brines as well as knowledge of snow cover and carbon chemistry in the ice are essential to estimate the partial pressure of pCO2 and CO2 flux. Further investigations of surface structure and snow cover and driving parameters such as heat flux, radiation, ice temperature and brine processes are required to adequately parameterize the surface resistance.

Description: We apply a flux parameterisation commonly used over terrestrial areas for calculation of CO2 fluxes over sea ice surfaces. The parameterisation is based on resistance analogy, and is evaluated and tested on data from seasonal fast sea ice, and the different variables influencing the exchange of CO2 between the atmosphere and ice are investigated. We found the flux to be small during the late winter with fluxes in both directions. Not surprisingly we find that the resistance across the surface controls the fluxes and detailed knowledge of the brine volume and carbon chemistry within the brines as well as knowledge of snow cover and carbon chemistry in the ice are essential to estimate the partial pressure of pCO2 and CO2 flux. Further investigations of surface structure and snow cover and driving parameters like heat flux, radiation, ice temperature and brine processes are required to adequately parameterize the surface resistance.

Description: A major issue of Arctic marine science is to understand whether the Arctic Ocean is, or will be, a source or sink for air-sea CO2 exchange. This has been complicated by the recent discoveries of ikaite (CaCO3·6H2O) in Arctic and Antarctic sea ice, which indicate that multiple chemical transformations occur in sea ice with a possible effect on CO2 and pH conditions in surface waters. Here we report on biogeochemical conditions, microscopic examinations and x-ray diffraction analysis of single crystals from an actively melting 1.7 km2 (0.5–1 m thick) drifting ice floe in the Fram Strait during summer. Our findings show that ikaite crystals are present throughout the sea ice but with larger crystals appearing in the upper ice layers. Ikaite crystals placed at elevated temperatures gradually disintegrated into smaller crystallites and dissolved. During our field campaign in late June, melt reduced the ice flow thickness by ca. 0.2 m per week and resulted in an estimated 1.6 ppm decrease of pCO2 in the ocean surface mixed layer. This corresponds to an air-sea CO2 uptake of 11 mmol m−2 sea ice d−1 or to 3.5 ton km−2 ice floe week−1.

Description: The precipitation of ikaite (CaCO3 ⋅ 6H2O) in polar sea ice is critical to the efficiency of the sea ice-driven carbon pump and potentially important to the global carbon cycle, yet the spatial and temporal occurrence of ikaite within the ice is poorly known. We report unique observations of ikaite in unmelted ice and vertical profiles of ikaite abundance and concentration in sea ice for the crucial season of winter. Ice was examined from two locations: a 1 m thick land-fast ice site and a 0.3 m thick polynya site, both in the Young Sound area (74° N, 20° W) of NE Greenland. Ikaite crystals, ranging in size from a few μm to 700 μm, were observed to concentrate in the interstices between the ice platelets in both granular and columnar sea ice. In vertical sea ice profiles from both locations, ikaite concentration determined from image analysis, decreased with depth from surface-ice values of 700–900 μmol kg−1 ice (~25 × 106 crystals kg−1) to values of 100–200 μmol kg−1 ice (1–7 × 106 crystals kg−1) near the sea ice–water interface, all of which are much higher (4–10 times) than those reported in the few previous studies. Direct measurements of total alkalinity (TA) in surface layers fell within the same range as ikaite concentration, whereas TA concentrations in the lower half of the sea ice were twice as high. This depth-related discrepancy suggests interior ice processes where ikaite crystals form in surface sea ice layers and partly dissolve in layers below. Melting of sea ice and dissolution of observed concentrations of ikaite would result in meltwater with a pCO2 of

Description: A major issue of Arctic marine science is to understand whether the Arctic Ocean is, or will be, a source or sink for air–sea CO2 exchange. This has been complicated by the recent discoveries of ikaite (a polymorph of CaCO3·6H2O) in Arctic and Antarctic sea ice, which indicate that multiple chemical transformations occur in sea ice with a possible effect on CO2 and pH conditions in surface waters. Here, we report on biogeochemical conditions, microscopic examinations and x-ray diffraction analysis of single crystals from a melting 1.7 km2 (0.5–1 m thick) drifting ice floe in the Fram Strait during summer. Our findings show that ikaite crystals are present throughout the sea ice but with larger crystals appearing in the upper ice layers. Ikaite crystals placed at elevated temperatures disintegrated into smaller crystallites and dissolved. During our field campaign in late June, melt reduced the ice floe thickness by 0.2 m per week and resulted in an estimated 3.8 ppm decrease of pCO2 in the ocean surface mixed layer. This corresponds to an air–sea CO2 uptake of 10.6 mmol m−2 sea ice d−1 or to 3.3 ton km−2 ice floe week−1. This is markedly higher than the estimated primary production within the ice floe of 0.3–1.3 mmol m−2 sea ice d−1. Finally, the presence of ikaite in sea ice and the dissolution of the mineral during melting of the sea ice and mixing of the melt water into the surface oceanic mixed layer accounted for half of the estimated pCO2 uptake.

Description: The precipitation of ikaite (CaCO3·6H2O) in polar sea ice is critical to the efficiency of the sea ice-driven carbon pump and potentially important to the global carbon cycle, yet the spatial and temporal occurrence of ikaite within the ice is poorly known. We report unique observations of ikaite in unmelted ice and vertical profiles of ikaite abundance and concentration in sea ice for the crucial season of winter. Ice was examined from two locations: a 1 m thick land-fast ice site and a 0.3 m thick polynya site, both in the Young Sound area (74° N, 20° W) of NE Greenland. Ikaite crystals, ranging in size from a few µm to 700 µm were observed to concentrate in the interstices between the ice platelets in both granular and columnar sea ice. In vertical sea-ice profiles from both locations, ikaite concentration determined from image analysis, decreased with depth from surfaceice values of 700–900 µmol kg−1 ice (~ 25 × 106 crystals kg−1) to bottom-layer values of 100–200 µmol kg−1 ice (1–7 × 106 kg−1), all of which are much higher (4–10 times) than those reported in the few previous studies. Direct measurements of total alkalinity (TA) in surface layers fell within the same range as ikaite concentration whereas TA concentrations in bottom layers were twice as high. This depth-related discrepancy suggests interior ice processes where ikaite crystals form in surface sea ice layers and partly dissolved in bottom layers. From these findings and model calculations we relate sea ice formation and melt to observed pCO2 conditions in polar surface waters, and hence, the air-sea CO2 flux.

Description: This study uses the eddy correlation technique to examine fluxes across the ice-water interface. Temperature eddy correlation systems were used to determine rates of ice melting and freezing, and O2 eddy correlation systems were used to examine O2 exchange rates as driven by biological and physical processes. The research was conducted below 0.7 m thick sea ice in mid March 2010 in a southwest Greenland fjord and revealed low average rates of ice melt amounting to a maximum of 0.80 ± 0.09 mm d−1 (SE, n=31). The corresponding calculated O2 flux associated with release of O2 depleted melt water was less than 13 % of the average daily O2 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 during certain time periods, amounting to 66 % of total deployment time. The identification of these conditions was evaluated by examining the velocity and the linearity and stability of the cumulative flux. The examination of unstratified conditions through velocity and O2 spectra and their cospectra revealed characteristic fingerprints of well-developed turbulence. From the observed O2 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−2 s−1, and that the 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 ± 0.02 mmol O2 m−2 d−1 (SE, n=4) and a respiration rate of −2.13 mmol O2 m−2 d−1 (no SE, see text for details) leading to a net primary production of −1.45 ± 0.02 mmol O2 m−2 d−1 (SE, n=4). Modeling the observed fluxes allowed for the calculation of fluxes during time periods when no O2 fluxes were extracted. This application of the eddy correlation technique produced high temporal resolution O2 fluxes and ice melt rates that were measured without disturbing the environmental conditions while integrating over a large area of approximately 50 m2 which encompassed the highly variable activity and spatial distributions of sea ice algal communities.

Description: 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 O2 eddy correlation systems were used to examine O2 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−1. The O2 flux associated with release of O2 depleted melt water was less than 13 % of the average daily O2 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 O2 spectra and their cospectra revealed characteristic fingerprints of well-developed turbulence. From the measured O2 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−2 s−1, 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 O2 m−2 d−1 and a respiration rate of −2.13 mmol O2 m−2 d−1 leading to a net ecosystem metabolism of −1.45 mmol O2 m−2 d−1. This application of the eddy correlation technique produced high temporal resolution O2 fluxes and ice melt rates that were measured without disturbing the in situ environmental conditions while integrating over an area of approximately 50 m2 which incorporated the highly variable activity and spatial distributions of sea-ice communities.