Nicolas-Xavier Geilfus

Dynamics of pCO2 and related air-ice CO2 fluxes in the Arctic coastal zone (Amundsen Gulf, Beaufort Sea)

We present an Arctic seasonal survey of carbon dioxide partial pressure (pCO 2 ) dynamics within sea ice brine and related air-ice CO 2 fluxes. The survey was carried out from early spring to the beginning of summer in the Arctic coastal waters of the Amundsen Gulf. High concentrations of pCO 2 (up to 1834 matm) were observed in the sea ice in early April as a consequence of concentration of solutes in brines, CaCO 3 precipitation and microbial respiration. CaCO 3 precipitation was detected through anomalies in total alkalinity (TA) and dissolved inorganic carbon (DIC). This precipitation seems to have occurred in highly saline brine in the upper part of the ice cover and in bulk ice. As summer draws near, the ice temperature increases and brine pCO 3 shifts from a large supersaturation (1834 matm) to a marked undersaturation (down to almost 0 matm). This decrease was ascribed to brine dilution by ice meltwater, dissolution of CaCO 3 and photosynthesis during the sympagic algal bloom. The magnitude of the CO 2 fluxes was controlled by ice temperature (through its control on brine volume and brine channels connectivity) and the concentration gradient between brine and the atmosphere. However, the state of the ice-interface clearly affects air-ice CO 2 fluxes.

Southern Ocean CO2 sink: The contribution of the sea ice

We report first direct measurements of the partial pressure of CO2 (pCO2) within Antarctic pack sea ice brines and related CO2 fluxes across the air-ice interface. From late winter to summer, brines encased in the ice change from a CO2 large oversaturation, relative to the atmosphere, to a marked undersaturation while the underlying oceanic waters remains slightly oversaturated. The decrease from winter to summer of pCO2 in the brines is driven by dilution with melting ice, dissolution of carbonate crystals, and net primary production. As the ice warms, its permeability increases, allowing CO2 transfer at the air-sea ice interface. The sea ice changes from a transient source to a sink for atmospheric CO2. We upscale these observations to the whole Antarctic sea ice cover using the NEMO-LIM3 large-scale sea ice-ocean and provide first estimates of spring and summer CO2 uptake from the atmosphere by Antarctic sea ice. Over the spring-summer period, the Antarctic sea ice cover is a net sink of atmospheric CO2 of 0.029 Pg C, about 58% of the estimated annual uptake from the Southern Ocean. Sea ice then contributes significantly to the sink of CO2 of the Southern Ocean.

Consequences of change and variability in sea ice on marine ecosystem and biogeochemical processes during the 2007–2008 Canadian International Polar Year program

Change and variability in the timing and magnitude of sea ice geophysical and thermodynamic state have consequences on many aspects of the arctic marine system. The changes in both the geophysical and thermodynamic state, and in particular the timing of the development of these states, have consequences throughout the marine system. In this paper we review the ‘consequences’ of change in sea ice state on primary productivity, marine mammal habitats, and sea ice as a medium for storage and transport of contaminants and carbon exchange across the ocean-sea-ice-atmosphere interface based upon results from the International Polar Year. Pertinent results include: 1) conditions along ice edges can bring deep nutrient-rich ‘pacific’ waters into nutrient-poor surface waters along the arctic coast, affecting local food webs; 2) both sea ice thermodynamic and dynamic processes ultimately affect ringed seal/polar bear habitats by controlling the timing, location and amount of surface deformation required for ringed seal and polar bear preferred habitat 3) the ice edges bordering open waters of flaw leads are areas of high biological production and are observed to be important beluga habitat. 4) exchange of climate-active gases, including CO2, is extremely active in sea ice environments, and the overall question of whether the Arctic Ocean is (or will be) a source or sink for CO2 will be dependent on the balance of competing climate-change feedbacks.

First “in situ” determination of gas transport coefficients ( DO2, DAr, and DN2) from bulk gas concentration measurements (O2, N2, Ar) in natural sea ice

We report bulk gas concentrations of O2, N2, and Ar, as well as their transport coefficients, in natural landfast subarctic sea ice in southwest Greenland. The observed bulk ice gas composition was 27.5% O2, 71.4% N2, and 1.09% Ar. Most previous studies suggest that convective transport is the main driver of gas displacement in sea ice and have neglected diffusion processes. According to our data, brines were stratified within the ice, so that no convective transport could occur within the brine system. Therefore, diffusive transport was the main driver of gas migration. By analyzing the temporal evolution of an internal gas peak within the ice, we deduced the bulk gas transport coefficients for oxygen (DO2), argon (DAr), and nitrogen (DN2). The values fit to the few existing estimates from experimental work, and are close to the diffusivity values in water (10-5 cm2 s-1). We suggest that gas bubbles escaping from the brine to the atmosphereas the ice gets more permeable during meltcould be responsible for the previously reported high transport coefficients. These results underline that when there is no convective transport within the sea ice, the transport of gas by diffusion through the brines, either in the liquid or gaseous phases, is a major factor in controlling the ocean-atmosphere exchange.

Drivers of inorganic carbon dynamics in first-year sea ice: A model study

Sea ice is an active source or a sink for carbon dioxide (CO2), although to what extent is not clear. Here, we analyze CO2 dynamics within sea ice using a one-dimensional halothermodynamic sea ice model including gas physics and carbon biogeochemistry. The ice-ocean fluxes, and vertical transport, of total dissolved inorganic carbon (DIC) and total alkalinity (TA) are represented using fluid transport equations. Carbonate chemistry, the consumption, and release of CO2 by primary production and respiration, the precipitation and dissolution of ikaite (CaCO3·6H2O) and ice-air CO2 fluxes, are also included. The model is evaluated using observations from a 6 month field study at Point Barrow, Alaska, and an ice-tank experiment. At Barrow, results show that the DIC budget is mainly driven by physical processes, wheras brine-air CO2 fluxes, ikaite formation, and net primary production, are secondary factors. In terms of ice-atmosphere CO2 exchanges, sea ice is a net CO2 source and sink in winter and summer, respectively. The formulation of the ice-atmosphere CO2 flux impacts the simulated near-surface CO2 partial pressure (pCO2), but not the DIC budget. Because the simulated ice-atmosphere CO2 fluxes are limited by DIC stocks, and therefore <2 mmol m−2 d−1, we argue that the observed much larger CO2 fluxes from eddy covariance retrievals cannot be explained by a sea ice direct source and must involve other processes or other sources of CO2. Finally, the simulations suggest that near-surface TA/DIC ratios of ∼2, sometimes used as an indicator of calcification, would rather suggest outgassing.

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 Canadas western Arctic region by sea ice stage-of-development that ended in 2004. The annual evolution of sea ice by stage of development in Canadas 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.