The pack ice of Earth's polar oceans appears to be frozen white desert, devoid of life. However, beneath the snow lies a unique habitat for a group of bacteria and microscopic plants and animals that are encased in an ice matrix at low temperatures and light levels, with the only liquid being pockets of concentrated brines. Survival in these conditions requires a complex suite of physiological and metabolic adaptations, but sea-ice organisms thrive in the ice, and their prolific growth ensures they play a fundamental role in polar ecosystems. Apart from their ecological importance, the bacterial and algae species found in sea ice have become the focus for novel biotechnology, as well as being considered proxies for possible life forms on ice-covered extraterrestrial bodies.

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[1] We report on the discovery of the mineral ikaite (CaCO 3 Á6H 2 O) in sea-ice from the Southern Ocean. The precipitation of CaCO 3 during the freezing of seawater has previously been predicted from thermodynamic modelling, indirect measurements, and has been documented in artificial sea ice during laboratory experiments but has not been reported for natural sea-ice. It is assumed that CaCO 3 formation in sea ice may be important for a sea ice-driven carbon pump in ice-covered oceanic waters. Without direct evidence of CaCO 3 precipitation in sea ice, its role in this and other processes has remained speculative. The discovery of CaCO 3 Á6H 2 O crystals in natural sea ice provides the necessary evidence for the evaluation of previous assumptions and lays the foundation for further studies to help elucidate the role of ikaite in the carbon cycle of the seasonally sea icecovered regions.

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Despite being one of the largest biomes on earth, sea ice ecosystems have only received intensive study over the past 30 years. Sea ice is a unique habitat for assemblages of bacteria, algae, protists, and invertebrates that grow within a matrix dominated by strong gradients in temperature, salinity, nutrients, and UV and visible radiation. A suite of physiological adaptations allow these organisms to thrive in ice, where their enormous biomass makes them a fundamental component of polar ecosystems. Sea ice algae are an important energy and nutritional source for invertebrates such as juvenile krill, accounting for up to 25% of total annual primary production in ice-covered waters. The ability of ice algae to produce large amounts of UV absorbing compounds such as mycosporine-like amino acids makes them even more important to organisms like krill that can incorporate these sunscreens into their own tissues. Furthermore, the nutrient and light conditions in which sea ice algae thrive induce them to synthesize enhanced concentrations of polyunsaturated fatty acids, a vital constituent of the diet of grazing organisms, especially during winter. Finally, sea ice bacteria and algae have become the focus of biotechnology, and are being considered as proxies of possible life forms on ice-covered extraterrestrial systems. An analysis of how the balance between sea ice and pelagic production might change under a warming scenario indicates that when current levels of primary production and changes in the areas of sea ice habitats are taken into account, the expected 25% loss of sea ice over the next century would increase primary production in the Southern Ocean by approximately 10%, resulting in a slight negative feedback on climate warming.

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ABSTRACT. Ice-core and snow data from the Amundsen, Bellingshausen and Weddell Seas, Antarctica, show that the formation of superimposed ice and the development of seawater-filled gap layers with high algal standing stocks is typical of the perennial sea ice in summer. The coarse-grained and dense snow had salinities mostly below 0.1ù. A layer of fresh superimposed ice had a mean thickness of 0.04^0.12 m. Gap layers 0.04^0.08 m thick extended downwards from 0.02 to 0.14 m below the water level. These gaps were populated by diatom standing stocks up to 439 mg L^1 chlorophyll a. We propose a comprehensive heuristic model of summer processes, where warming and the reversal of temperature gradients cause major transformations in snow and ice properties. The warming also causes the reopening of incompletely frozen slush layers caused by flood^freeze cycles during winter. Alternatively, superimposed ice forms at the cold interface between snow and slush in the case of flooding with negative freeboard. Combined, these explain the initial formation of gap layers by abiotic means alone. The upward growth of superimposed ice above the water level competes with a steady submergence of floes due to bottom and internal melting and accumulation of snow.