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The chemistry of snow and ice cores from Svalbard is influenced by variations in local sea ice margin and distance to open water. Snow pits sampled at two summits of Vestfonna ice cap (Nordaustlandet, Svalbard), exhibit spatially heterogeneous soluble ions concentrations despite similar accumulation rates, reflecting the importance of small-scale weather patterns on this island ice cap. The snow pack on the western summit shows higher average values of marine ions and a winter snow layer that is relatively depleted in sulphate. One part of the winter snow pack exhibits a [SO4-/Na+] ratio reduced by two thirds compared with its ratio in sea water. This low sulphate content in winter snow is interpreted as the signature of frost flowers, which are formed on young sea ice when offshore winds predominate. Frost flowers have been described as the dominant source of sea salt to aerosol and precipitation in ice cores in coastal Antarctica but this is the first time their chemical signal has been described in the Arctic. The eastern summit does not show any frost flower signature and we interpret the unusually dynamic ice transport and rapid formation of thin ice on the Hinlopen Strait as the source of the frost flowers.

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The vegetation pattern of siliceous boulder snow beds (Dicranoweision crispulae all. nov. prov.) of Svalbard was investigated by using transect studies in several places on Spitsbergen. Dicranoweisia crispula is the best diagnostic species. It is found throughout the whole snow bed, is a good differential species against Racomitrium lanuginosum communities above the snow bed, and does not occur on basic rocks. Three Andreaea spp. are also among the most important members of these communities. They are all acidophilous, but with different pH preferences. Eight weakly acidophilous species lacking both on basic and on gneissic/granitic rocks, are reported from Svalbard. Half of these are characteristic species of Dicranoweision crispulae on Svalbard.

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Frost flowers have been proposed to be the major source of sea-salt aerosol to the atmosphere during polar winter and a source of reactive bromine during polar springtime. However little is known about their bulk chemical composition or microstructure, two important factors that may affect their ability to produce aerosols and provide chemically reactive surfaces for exchange with the atmosphere. Therefore, we chemically analyzed 28 samples of frost flowers and parts of frost flowers collected from sea ice off of northern Alaska. Our results support the proposed mechanism for frost flower growth that suggests water vapor deposition forms an ice skeleton that wicks brine present on newly grown sea ice. We measured a high variability in sulfate enrichment factors (with respect to chloride) in frost flowers and seawater from the vicinity of freezing sea ice. The variability in sulfate indicates that mirabilite precipitation (Na2SO4 x 10 H2O) occurs during frost flower growth. Brine wicked up by frost flowers is typically sulfate depleted, in agreement with the theory that frost flowers are related to sulfate-depleted aerosol observed in Antarctica. The bromide enrichment factors we measured in frost flowers are within error of seawater composition, constraining the direct reactive losses of bromide from frost flowers. We combined the chemical composition measurements with temperature observations to create a conceptual model of possible scenarios for frost flower microstructure development.

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Broadcast spawning marine invertebrates are susceptible to environmental stressors such as climate change, as their reproduction depends on the successful meeting and fertilization of gametes in the water column. Under near-future scenarios of ocean acidification, the swimming behaviour of marine invertebrate sperm is altered. We tested whether this was due to changes in sperm mitochondrial activity by investigating the effects of ocean acidification on sperm metabolism and swimming behaviour in the sea urchin Centrostephanus rodgersii. We used a fluorescent molecular probe (JC-1) and flow cytometry to visualize mitochondrial activity (measured as change in mitochondrial membrane potential, MMP). Sperm MMP was significantly reduced in delta pH -0.3 (35% reduction) and delta pH -0.5 (48% reduction) treatments, whereas sperm swimming behaviour was less sensitive with only slight changes (up to 11% decrease) observed overall. There was significant inter-individual variability in responses of sperm swimming behaviour and MMP to acidified seawater. We suggest it is likely that sperm exposed to these changes in pH are close to their tipping point in terms of physiological tolerance to acidity. Importantly, substantial inter-individual variation in responses of sperm swimming to ocean acidification may increase the scope for selection of resilient phenotypes, which, if heritable, could provide a basis for adaptation to future ocean acidification.