Description: Sea-ice ecosystems are among the most extensive of Earth’s habitats; yet its autotrophic and heterotrophic activities remain poorly constrained. We employed the in situ aquatic eddy-covariance (AEC) O2 flux method and laboratory incubation techniques (H14CO3−, [3H] thymidine and [3H] leucine) to assess productivity in Arctic sea-ice using different methods, in conditions ranging from land-fast ice during winter, to pack ice within the central Arctic Ocean during summer. Laboratory tracer measurements resolved rates of bacterial C demand of 0.003–0.166 mmol C m−2 day−1 and primary productivity rates of 0.008–0.125 mmol C m−2 day−1 for the different ice floes. Pack ice in the central Arctic Ocean was overall net autotrophic (0.002–0.063 mmol C m−2 day−1), whereas winter land-fast ice was net heterotrophic (− 0.155 mmol C m−2 day−1). AEC measurements resolved an uptake of O2 by the bottom-ice environment, from ~ − 2 mmol O2 m−2 day−1 under winter land-fast ice to~ − 6 mmol O2 m−2 day−1 under summer pack ice. Flux of O2-deplete meltwater and changes in water flow velocity masked potential biological-mediated activity. AEC estimates of primary productivity were only possible at one study location. Here, productivity rates of 1.3 ± 0.9 mmol O2 m−2 day−1, much larger than concurrent laboratory tracer estimates (0.03 mmol C m−2 day−1), indicate that ice algal production and its importance within the marine Arctic could be underestimated using traditional approaches. Given careful flux interpretation and with further development, the AEC technique represents a promising new tool for assessing oxygen dynamics and sea-ice productivity in ice-covered regions.

Description: Antarctic krill Euphausia superba (“krill”) constitute a fundamental food source for Antarctic seabirds and mammals, and a globally important fisheries resource. The future resilience of krill to climate change depends critically on the winter survival of young krill. To survive periods of extremely low production by pelagic algae during winter, krill are assumed to rely partly on carbon produced by ice algae. The true dependency on ice algae-produced carbon, however, is so far unquantified. This confounds predictions on the future resilience of krill stocks to sea ice decline. Fatty acid (FA) analysis, bulk stable isotope analysis (BSIA), and compound-specific stable isotope analysis (CSIA) of diatom- and dinoflagellate-associated marker FAs were applied to quantify the dependency of overwintering larval, juvenile, and adult krill on ice algae-produced carbon (αIce) during winter 2013 in the Weddell-Scotia Confluence Zone. Our results demonstrate that the majority of the carbon uptake of the overwintering larval and juvenile krill originated from ice algae (up to 88% of the carbon budget), and that the dependency on ice algal carbon decreased with ontogeny, reaching 〈56% of the carbon budget in adults. Spatio-temporal variability in the utilization of ice algal carbon was more pronounced in larvae and juvenile krill than in adults. Differences between αIce estimates derived from short- vs. long-term FA-specific isotopic compositions suggested that ice algae-produced carbon gained importance as the winter progressed, and might become critical at the late winter-spring transition, before the phytoplankton bloom commences. Where the sea ice season shortens, reduced availability of ice algae might possibly not be compensated by surplus phytoplankton production during wintertime. Hence, sea ice decline could seriously endanger the winter survival of recruits, and subsequently overall biomass of krill.

Description: Sea-ice ecosystems are among the most extensive of Earth’s habitats; yet its autotrophic and heterotrophic activities remain poorly constrained. We employed the in situ aquatic eddy-covariance (AEC) O2 flux method and laboratory incubation techniques (H14CO3−, [3H] thymidine and [3H] leucine) to assess productivity in Arctic sea-ice using different methods, in conditions ranging from land-fast ice during winter, to pack ice within the central Arctic Ocean during summer. Laboratory tracer measurements resolved rates of bacterial C demand of 0.003–0.166 mmol C m−2 day−1 and primary productivity rates of 0.008–0.125 mmol C m−2 day−1 for the different ice floes. Pack ice in the central Arctic Ocean was overall net autotrophic (0.002–0.063 mmol C m−2 day−1), whereas winter land-fast ice was net heterotrophic (− 0.155 mmol C m−2 day−1). AEC measurements resolved an uptake of O2 by the bottom-ice environment, from ~ − 2 mmol O2 m−2 day−1 under winter land-fast ice to~ − 6 mmol O2 m−2 day−1 under summer pack ice. Flux of O2-deplete meltwater and changes in water flow velocity masked potential biological-mediated activity. AEC estimates of primary productivity were only possible at one study location. Here, productivity rates of 1.3 ± 0.9 mmol O2 m−2 day−1, much larger than concurrent laboratory tracer estimates (0.03 mmol C m−2 day−1), indicate that ice algal production and its importance within the marine Arctic could be underestimated using traditional approaches. Given careful flux interpretation and with further development, the AEC technique represents a promising new tool for assessing oxygen dynamics and sea-ice productivity in ice-covered regions.

Description: Survival of larval Antarctic krill (Euphausia superba) during winter is largely dependent upon the presence of sea ice as it provides an important source of food and shelter. We hypothesized that sea ice provides additional benefits because it hosts fewer competitors and provides reduced predation risk for krill larvae than the water column. To test our hypothesis, zooplankton were sampled in the Weddell-Scotia Confluence Zone at the ice-water interface (0–2 m) and in the water column (0–500 m) during August–October 2013. Grazing by mesozooplankton, expressed as a percentage of the phytoplankton standing stock, was higher in the water column (1.97 ± 1.84%) than at the ice-water interface (0.08 ± 0.09%), due to a high abundance of pelagic copepods. Predation risk by carnivorous macrozooplankton, expressed as a percentage of the mesozooplankton standing stock, was significantly lower at the ice-water interface (0.83 ± 0.57%; main predators amphipods, siphonophores and ctenophores) than in the water column (4.72 ± 5.85%; main predators chaetognaths and medusae). These results emphasize the important role of sea ice as a suitable winter habitat for larval krill with fewer competitors and lower predation risk. These benefits should be taken into account when considering the response of Antarctic krill to projected declines in sea ice. Whether reduced sea-ice algal production may be compensated for by increased water column production remains unclear, but the shelter provided by sea ice would be significantly reduced or disappear, thus increasing the predation risk on krill larvae.

Description: In this study, we present unique data collected with a Surface and Under-Ice Trawl (SUIT) during five campaigns between 2012 and 2017, covering the spring to summer and autumn transition in the Arctic Ocean, and the seasons of winter and summer in the Southern Ocean. The SUIT was equipped with a sensor array from which we retrieved: sea-ice thickness, the light field at the underside of sea ice, chlorophyll a concentration in the ice (in-ice chl a), and the salinity, temperature, and chl a concentration of the under-ice water. With an average trawl distance of about 2 km, and a global transect length of more than 117 km in both polar regions, the present work represents the first multi-seasonal habitat characterization based on kilometer-scale profiles. The present data highlight regional and seasonal patterns in sea-ice properties in the Polar Ocean. Light transmittance through Arctic sea ice reached almost 100 in summer, when the ice was thinner and melt ponds spread over the ice surface. However, the daily integrated amount of light under sea ice was maximum in spring. Compared to the Arctic, Antarctic sea-ice was thinner, snow depth was thicker, and sea-ice properties were more uniform between seasons. Light transmittance was low in winter with maximum transmittance of 73. Despite thicker snow depth, the overall under-ice light was considerably higher during Antarctic summer than during Arctic summer. Spatial autocorrelation analysis shows that Arctic sea ice was characterized by larger floes compared to the Antarctic. In both Polar regions, the patch size of the transmittance followed the spatial variability of sea-ice thickness. In-ice chl a in the Arctic Ocean remained below 0.39 mg chl a m〈sup〉â��2〈/sup〉, whereas it exceeded 7 mg chl a m〈sup〉â��2〈/sup〉 during Antarctic winter, when water chl a concentrations remained below 1.5 mg chl a m〈sup〉â��2〈/sup〉, thus highlighting its potential as an important carbon source for overwintering organisms. The data analyzed in this study can improve large-scale physical and ecosystem models, habitat mapping studies and time series analyzed in the context of climate change effects and marine management.

Description: During the 2018 Multidisciplinary Arctic Program‐Last Ice in the Lincoln Sea, we sampled 45 multiyear ice (MYI) and 34 first‐year ice (FYI) cores, combined with snow depth, ice thickness, and transmittance surveys from adjacent level FYI and undeformed MYI. FYI sites show a decoupling between bottom‐ice chlorophyll a (chl a) and snow depth; however, MYI showed a significant correlation between ice‐algal chl a biomass and snow depth. Topographic control of the snow cover resulted in greater spatiotemporal variability of the snow over the level FYI, and consequently transmittance, compared to MYI with an undulating surface. The coupled patterns of snow depth, transmittance, and chl a indicate that MYI provides an environment with more stable light conditions for ice algal growth. The importance of sea ice surface topography for ice algal habitat underpins the potential ecological changes associated with projected increased ice dynamics and deformation.

Description: Sea ice is one of the main features influencing the Arctic marine protist community composition and diversity in sea ice and sea water. We analyzed protist communities within sea ice, melt pond water, under-ice water and deep-chlorophyll maximum water at eight sea ice stations sampled during summer of the 2012 record sea ice minimum year. Using Illumina sequencing, we identified characteristic communities associated with specific habitats and investigated protist exchange between these habitats. The highest abundance and diversity of unique taxa were found in sea ice, particularly in multi-year ice (MYI), highlighting the importance of sea ice as a unique habitat for sea ice protists. Melting of sea ice was associated with increased exchange of communities between sea ice and the underlying water column. In contrast, sea ice formation was associated with increased exchange between all four habitats, suggesting that brine rejection from the ice is an important factor for species redistribution in the Central Arctic. Ubiquitous taxa (e.g. Gymnodinium) that occurred in all habitats still had habitat-preferences. This demonstrates a limited ability to survive in adjacent but different environments. Our results suggest that the continued reduction of sea ice extent, and particularly of MYI, will likely lead to diminished protist exchange and subsequently, could reduce species diversity in all habitats of the Central Arctic Ocean. An important component of the unique sea ice protist community could be endangered because specialized taxa restricted to this habitat may not be able to adapt to rapid environmental changes.

Description: Assessing the role of sea ice algal biomass and primary production for polar ecosystems remains challenging due to the strong spatio-temporal variability of sea ice algae. Therefore, the spatial representativeness of sea ice algal biomass and primary production sampling remains a key issue in large-scale models and climate change predictions of polar ecosystems. To address this issue, we presented two novel approaches to up-scale ice algal chl a biomass and net primary production (NPP) estimates based on profiles covering distances of 100 to 1,000 s of meters. This was accomplished by combining ice core-based methods with horizontal under-ice spectral radiation profiling conducted in the central Arctic Ocean during summer 2012. We conducted a multi-scale comparison of ice-core based ice algal chl a biomass with two profiling platforms: a remotely operated vehicle and surface and under ice trawl (SUIT). NPP estimates were compared between ice cores and remotely operated vehicle surveys. Our results showed that ice core-based estimates of ice algal chl a biomass and NPP do not representatively capture the spatial variability compared to the remotely operated vehicle-based estimates, implying considerable uncertainties for pan-Arctic estimates based on ice core observations alone. Grouping sea ice cores based on region or ice type improved the representativeness. With only a small sample size, however, a high risk of obtaining non-representative estimates remains. Sea ice algal chl a biomass estimates based on the dominant ice class alone showed a better agreement between ice core and remotely operated vehicle estimates. Grouping ice core measurements yielded no improvement in NPP estimates, highlighting the importance of accounting for the spatial variability of both the chl a biomass and bottom-ice light in order to get representative estimates. Profile-based measurements of ice algae chl a biomass identified sea ice ridges as an underappreciated component of the Arctic ecosystem because chl a biomass was significantly greater in this unique habitat. Sea ice ridges are not easily captured with ice coring methods and thus require more attention in future studies. Based on our results, we provide recommendations for designing an efficient and effective sea ice algal sampling program for the summer season.