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Schnack-Schiel, S. B., Dieckmann, G. S., Gradinger, R., Melnikov, I. A., Spindler, M., & Thomas, D. N. (2001). Meiofauna in sea ice of the Weddell Sea (Antarctica). Polar Biol, 24(10), 724–728.
Abstract: Sea-ice meiofauna was studied during various cruises to the Weddell Sea. Foraminifers dominate (75%) the sea-ice community in terms of numerical abundance while turbellarians dominate (45%) in terms of biomass. Distribution of organisms is patchy and varies considerably between cruises but also between sampling sites within one cruise. The bulk of the meiofauna is concentrated in the lowest parts of the sea ice, especially during winter and autumn. However, in porous summer sea ice, sympagic organisms also occur in high densities in upper and intermediate layers of sea ice. Proto- and metazoans associated with Antarctic sea ice include organisms actually living in sea ice, as well as those on the underside of floes and in the underlying water. The sea-ice habitat serves as a feeding ground, as well as an important nursery for juveniles, providing energy-rich food resources. The ice also constitutes a shelter from predators.
Keywords: Sea ice biota; Foraminifera; Antarctic sea ice; Sea ice; Meiofauna; Community composition; Meiobenthos; Antarctic zone; Juveniles; Psw; Weddell Sea; Antarctica
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Mock, T., Dieckmann, G. S., Haas, C., Krell, A., Tison, J. - L., Belem, A. L., et al. (2002). Micro-optodes in sea ice: a new approach to investigate oxygen dynamics during sea ice formation. Aquat Microb Ecol, 29(3), 297–306.
Abstract: Oxygen micro-optodes were used to measure oxygen dynamics directly within the microstructure of sea ice by freezing the sensors into the ice during its formation. The experiment was conducted in a 4 m³ mesocosm filled with artificial seawater and inoculated with a unialgal culture of the common Antarctic ice diatom Fragilariopsis cylindrus (Bacillariophyceae) to a final chlorophyll a (chl a) concentration of 11 µg 1?¹. Ice growth was initiated 7 d after inoculation by reducing the air temperature to -10 plus or minus 2 degree C and terminated 17 d later. The final ice thickness was 27 cm. One optode was frozen into grease ice and 2 others into the skeletal layer of the growing ice sheet. Increasing oxygen concentrations during ice crystal formation at the water surface and the ice-water interface revealed a strong inclusion of oxygen, which was either physically trapped and/or the result of photosynthesising diatoms. The major portion of oxygen was present as gas bubbles due to super-saturation as a result of increasing salinity and oxygen production by diatoms. An increase in salinity due to a concurrent decrease in ice temperatures during subsequent sea ice development reduced the maximum concentration of dissolved oxygen within brine. Thus, dissolved oxygen concentrations decreased over time, whereas gaseous oxygen was released to the atmosphere and seawater. The sensors are a significant advance on more conventional microelectrodes, because the recordings can be temperature and salinity compensated in order to obtain precise measurements of oxygen dynamics with regard to total (dissolved and gaseous) and dissolved oxygen in sea ice. Optodes do not consume oxygen during measuremnet over a long period under extreme conditions, which is another advantage for long-term deployment in the field.
Keywords: Fragilariopsis cylindrus; Oxygen; Methods; Micro-optodes; Sea ice; Biogeochemistry; Diatoms; Algae; Chlorophyll; Photosynthesis; Salinity effects; Sea water; Marine ecosystems; Chlorophylls; Dissolved oxygen; Gases; Epontic environment; Electrodes; Sensors; Brines; Ice-water interface; Ice formation; Bacillariophyceae
Notes: Marine
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Kennedy, H., Thomas, D. N., Kattner, G., Haas, C., & Dieckmann, G. S. (2002). Particulate organic matter in Antarctic summer sea ice: concentration and stable isotopic composition. Mar Ecol Prog Ser, 238, 1–13.
Abstract: The chemical and isotopic data from sea ice collected over a wide area of the Weddell Sea, Antarctica, during the austral summer/early autumn illustrate the range of environmental conditions under which ice algae grow. A range of ice types and features were sampled including intact and layered ice floes and surface ponds. Sea ice communities were found in all these environments but the highest biomasses were found either at the base of ice floes, or in the interior of layered floes with quasi-continuous horizontal gaps at or shortly below the water level. In the layered floes, particulate organic carbon (POC) measured in the ice layer immediately overlying the gap water (280 to 6014 µmol dm?³) was in excess of what would be predicted if algal growth had occurred in a closed environment. The chemical composition of the gap water was strongly affected by biological activity in the overlying ice, which acts as a physical support for the algae retained within its matrix. The lowest range of POC (27 to 739 µmol dm?³) conformed to predictions of algal growth in a closed system and samples were collected from the interior of ice floes where there was essentially no potential for nutrient exchange. The surface ponds displayed nitrate (NO³?) exhaustion and total dissolved inorganic carbon (?CO?) reductions consistent with nutrient limited algal growth. The stable carbon isotopic composition of the particulate organic matter (POM) across all habitat types sampled (?¹³CPOC -10.0 to -27.3?) displayed a wide range but was much less variable than the range of POC concentrations might have implied. The assumption that the highest biomass of algae in sea ice will result in the most positive ?¹³CPOC values cannot be generally applied. The isotopic composition of dissolved inorganic carbon (?¹³C?CO?) in gap waters and surface ponds varied from 0.15 to 3.0? and was shown to be commensurate with the changes predicted from NO³? deficits caused by algal growth.
Keywords: Pom; Anarctic sea ice; ice microalgae; carbon isotopic composition
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Thomas, D. N. (2005). Photosynthetic microbes in freezing deserts. Trends Microbiol, 13(3), 87–88.
Abstract: Polar deserts are not devoid of life despite the extreme low temperature and scarcity of water. Recently, patterned stone fields – caused by periglacial activity – have been surveyed in the Arctic and Antarctic. It was found that the productivity of the cyanobacteria and algae (hypoliths) that colonise the underside of the stones is strongly related to the pattern of the stones. The hypolith assemblages were in some cases as productive as lichens, bryophytes and plants that resided nearby.
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Gleitz, M., & Thomas, D. N. (1992). Physiological responses of a small Antarctic diatom (Chaetoceros sp.) to simulated environmental constraints associated with sea-ice formation. Mar Ecol Prog Ser, 88(2-3), 271–278.
Abstract: The physiological responses of a small unicellular Chaetoceros species, isolated from the Weddell Sea, Antarctica, to changes in temperature, salinity and irradiance simulating those that occur during new-ice formation were investigated. The combination of increased salinity, increased quantum irradiance and decreased temperature significantly reduced growth and photosynthetic rates compared to the control, although cellular metabolism was not inhibited. The cells retained the capacity to photoacclimate, which was observed in the variations in cellular chlorophyll a concentrations and carbon allocation patterns. In terms of photosynthesis, a doubling of quantum irradiance apparently compensated for the adverse effects of increased salinity and lowered temperature. It is thus hypothesized that at least some species of the late season phytoplankton population survive incorporation into ice and continue to photosynthesize and grow under the extreme conditions encountered during sea-ice formation.
Keywords: plant physiology; abiotic factors; temperature effects; salinity effects; irradiance; sea ice; growth; photosynthesis; Chaetoceros; Psw; Weddell Sea; simulation
Notes: Bibliogr.: 38 ref.; Marine
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