Biogeochemical cycle in a coccolithophorid bloom

The biogeochemical properties of an extensive bloom of the coccolithophore, Emiliania huxleyi, at the shelf break in the northern Gulf of Biscay was investigated in June 2006. Total Alkalinity (TA) values in the water column showed strong non-conservative behaviour indicative of the impact of calcification, with the highest TA anomalies (up to 26μmol.kg-1) in the high reflectance coccolith patch. Partial pressure of CO2 (pCO2) values ranged from 250 to 338μatm and the area was found to act as a sink for atmospheric CO2.Overall, pCO2@13°C (pCO2 normalized at a constant temperature of 13°C) in the water column was negatively related to TA anomalies in agreement with an overall production of CO2 related to calcification. Hence, the calcifying phase of the E. huxleyi bloom decreased the sink of atmospheric pCO2, but did not reverse the direction of the flux. Rates of pelagic respiration up to 5.5mmol O2.m-3.d-1 suggested a close coupling between primary production and respiration and/or between organic carbon content and respiration. Benthic respiration rates were quite low and varied between 2 and 9mmol O2.m-3.d-1, in agreement with the fact that the study area consists of sandy sediments with low organic matter content. Benthic respiration was well correlated to the chlorophyll a content of the top 1cm of the sediment cores. Evidence was found for dissolution of CaCO3 due to the acidification of superficial sediments in relation to the production of CO2 and the oxidation of H2S in the oxic layers

CO2 and CH4 in sea ice from a subarctic fjord under influence of riverine input

We present the CH4 concentration [CH4], the partial pressure of CO2 (pCO2) and the total gas content in bulk sea ice from subarctic, land-fast sea ice in the Kapisillit fjord, Greenland. Fjord systems are characterized by freshwater runoff and riverine input and based on dδ18O data, we show that > 30% of the surface water originated from periodic river input during ice growth. This resulted in fresher sea-ice layers with higher gas content than is typical from marine sea ice. The bulk ice [CH4] ranged from 1.8 to 12.1 nmol Lg-1, which corresponds to a partial pressure ranging from 3 to 28 ppmv. This is markedly higher than the average atmospheric methane content of 1.9 ppmv. Evidently most of the trapped methane within the ice was contained inside bubbles, and only a minor portion was dissolved in the brines. The bulk ice pCO2 ranged from 60 to 330 ppmv indicating that sea ice at temperatures above -4 °C is undersaturated compared to the atmosphere (390 ppmv). This study adds to the few existing studies of CH4 and CO2 in sea ice, and we conclude that subarctic seawater can be a sink for atmospheric CO2, while being a net source of CH4

Evidence of Freezing Pressure in Sea Ice Discrete Brine Inclusions and Its Impact on Aqueous-Gaseous Equilibrium

Sea ice in part controls surface water properties and the ocean-atmosphere exchange of greenhouse gases at high latitudes. In sea ice, gas exists dissolved in brine and as air bubbles contained in liquid brine inclusions or as bubbles trapped directly within the ice matrix. Current research on gas dynamics within the ocean-sea ice-atmosphere interface has been based on the premise that brine with dissolved air becomes supersaturated with respect to the atmosphere during ice growth. Based on Henry's law, gas bubbles within brine should grow when brine reaches saturation during cooling, given that the total partial pressure of atmospheric gases is above the implicit pressure in brine of 1 atm. Using high-resolution light microscopy time series imagery of gas bubble evolution inside discrete brine pockets, we observed bubbles shrinking during cooling events in response to the development of freezing pressure above 3 atm. During warming of discrete brine pockets, existing bubbles expand and new bubbles nucleate in response to depressurization. Pressure variation within these inclusions has direct impacts on aqueous-gaseous equilibrium, indicating that Henry's law at a constant pressure of 1 atm is inadequate to assess the partitioning between dissolved and gaseous fractions of gas in sea ice. This new evidence of pressure build-up in discrete brine inclusions controlling the solubility of gas and nucleation of bubbles in these inclusions has the potential to affect the transport pathways of air bubbles and dissolved gases within sea ice-ocean-atmosphere interface and modifies brine biochemical properties

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)

Where does the methane entrapped in Antarctic sea ice come from?

info:eu-repo/semantics/publishe

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

Whole-system metabolism and CO₂ fluxes in a Mediterranean Bay dominated by seagrass beds (Palma Bay, NW Mediterranean)

The relationship between whole-system metabolism estimates based on planktonic and benthic incubations (bare sediments and seagrass, Posidonia oceanica meadows), and CO2 fluxes across the air-sea interface were examined in the Bay of Palma (Mallorca, Spain) during two cruises in March and June 2002. Moreover, planktonic and benthic incubations were performed at monthly intervals from March 2001 to October 2002 in a seagrass vegetated area of the bay. From the annual study, results showed a contrast between the planktonic compartment, which was heterotrophic during most of the year, except for occasional bloom episodes, and the benthic compartment, which was slightly autotrophic. Whereas the seagrass community was autotrophic, the excess organic carbon production therein could only balance the excess respiration of the planktonic compartment in shallow waters (<10 m) relative to the maximum depth of the bay (55 m). This generated a horizontal gradient from autotrophic or balanced communities in the shallow, seagrass-covered areas of the bay, to strongly heterotrophic communities in deeper areas, consistent with the patterns of CO2 fields and fluxes across the bay observed during the two extensive cruises in 2002. Finally, dissolved inorganic carbon and oxygen budgets provided NEP estimates in fair agreement with those derived from direct metabolic estimates based on incubated samples over the Posidonia oceanica meadow

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