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Interactions between the Southern Ocean and the Weddell Sea ice shelves are important both to the Antarctic Ice Sheet and to the production of globally significant water masses. Here we review the interaction between the Filchner-Ronne Ice Shelf and the shelf sea in which it floats. The continental shelf processes leading to the production of Weddell Sea deep and bottom waters from the original off-shelf source waters are discussed, and a new view is offered of the initial production of High-Salinity Shelf Water. Data from ship-based measurements at the ice front, from glaciological methods, and from measurements made within the sub–ice shelf cavity itself are used to describe the pattern of flows beneath the ice shelf. We also consider the variability observed within the cavity from tidal to interannual time scales and finish with a discussion of future research priorities in the region.

Observations of snow properties, superimposed ice, and atmospheric heat fluxes have been performed on first-year and second-year sea ice in the western Weddell Sea, Antarctica. Snow in this region is particular as it does usually survive summer ablation. Measurements were performed during Ice Station Polarstern (ISPOL), a 5-week drift station of the German icebreaker RV Polarstern. Net heat flux to the snowpack was 8 W m−2, causing only 0.1 to 0.2 m of thinning of both snow cover types, thinner first-year and thicker second-year snow. Snow thinning was dominated by compaction and evaporation, whereas melt was of minor importance and occurred only internally at or close to the surface. Characteristic differences between snow on first-year and second-year ice were found in snow thickness, temperature, and stratigraphy. Snow on second-year ice was thicker, colder, denser, and more layered than on first-year ice. Metamorphism and ablation, and thus mass balance, were similar between both regimes, because they depend more on surface heat fluxes and less on underground properties. Ice freeboard was mostly negative, but flooding occurred mainly on first-year ice. Snow and ice interface temperature did not reach the melting point during the observation period. Nevertheless, formation of discontinuous superimposed ice was observed. Color tracer experiments suggest considerable meltwater percolation within the snow, despite below-melting temperatures of lower layers. Strong meridional gradients of snow and sea-ice properties were found in this region. They suggest similar gradients in atmospheric and oceanographic conditions and implicate their importance for melt processes and the location of the summer ice edge.

The available ecological and palaeoecological information for two sea ice-related marine diatoms (Bacillariophyceae), Thalassiosira antarctica Comber and Porosira glacialis (Grunow) Jørgensen, suggests that these two species have similar sea surface temperature (SST), sea surface salinity (SSS) and sea ice proximity preferences. From phytoplankton observations, both are described as summer or autumn bloom species, commonly found in low SST waters associated with sea ice, although rarely within the ice. Both species form resting spores (RS) as irradiance decreases, SST falls and SSS increases in response to freezing ice in autumn. Recent work analysing late Quaternary seasonally laminated diatom ooze from coastal Antarctic sites has revealed that sub-laminae dominated either by T. antarctica RS, or by P. glacialis RS, are nearly always deposited as the last sediment increment of the year, interpreted as representing autumn flux. In this study, we focus on sites from the East Antarctic margin and show that there is a spatial and temporal separation in whether T. antarctica RS or P. glacialis RS form the autumnal sub-laminae. For instance, in deglacial sediments from the Mertz Ninnis Trough (George V Coast) P. glacialis RS form the sub-laminae whereas in similar age sediments from Iceberg Alley (Mac.Robertson Shelf) T. antarctica RS dominate the autumn sub-lamina. In the Dumont d'Urville Trough (Adélie Land), mid-Holocene (Hypsithermal warm period) autumnal sub-laminae are dominated by T. antarctica RS whereas late Holocene (Neoglacial cool period) sub-laminae are dominated by P. glacialis RS. These observations from late Quaternary seasonally laminated sediments would appear to indicate that P. glacialis prefers slightly cooler ocean–climate conditions than T. antarctica. We test this relationship against two down-core Holocene quantitative diatom abundance records from Dumont d'Urville Trough and Svenner Channel (Princess Elizabeth Land) and compare the results with SST and sea ice concentration results of an Antarctic and Southern Ocean Holocene climate simulation that used a coupled atmosphere–sea ice–vegation model forced with orbital parameters and greenhouse gas concentrations. We find that abundance of P. glacialis RS is favoured by higher winter and spring sea ice concentrations and that a climatically-sensitive threshold exists between the abundance of P. glacialis RS and T. antarctica RS in the sediments. An increase to >0.1 for the ratio of P. glacialis RS:T. antarctica RS indicates a change to increased winter sea ice concentration (to >80% concentration), cooler spring seasons with increased sea ice, slightly warmer autumn seasons with less sea ice and a change from ~7.5months annual sea ice cover at a site to much greater than 7.5months. In the East Antarctic sediment record, an increase in the ratio from <0.1 to above 0.1 occurs at the transition from the warmer Hypsithermal climate into the cooler Neoglacial climate (~4cal kyr) indicating that the ratio between these two diatoms has the potential to be used as a semi-quantitative climate proxy.

Several biogeographical studies have already been performed on the ascidians of the Antarctic region. However, new data obtained in the last few years have led us to a revision of the biogeography of this fauna. To examine the biogeographical structure of the Antarctic region, we divided it into 10 sectors, depending on the principal geographical features, and then applied cluster analysis and a multi-dimensional scaling ordination to a presence/absence matrix of species for each biogeographical area. Our study shows that Antarctic ascidians are a very homogeneous fauna, with a high level of endemism in the whole region (25–51% of Antarctic endemic species per sector), but with a low percentage of sector endemism (only up to 10%). This probably results from isolation arising from the Antarctic Convergence, and the vast geographical distances from adjacent regions, as well as from the relative constancy of the hydrographical conditions and the dispersal of organisms through circumpolar currents. In fact, cosmopolitan species represented only 0–7% of the total ascidian fauna in all sectors. Only the Bellingshausen Sea (low sample size), Bouvetøya (young and isolated, with an impoverished ascidian fauna) and the South Sandwich Islands (also young and isolated) are relatively separated. The insular sectors were more closely related to the South America and sub- Antarctic regions than the continental ones, showing a latitudinal gradient.

The oceans play a key role in climate regulation especially in part buffering (neutralising) the effects of increasing levels of greenhouse gases in the atmosphere and rising global temperatures. This chapter examines how the regulatory processes performed by the oceans alter as a response to climate change and assesses the extent to which positive feedbacks from the ocean may exacerbate climate change. There is clear evidence for rapid change in the oceans. As the main heat store for the world there has been an accelerating change in sea temperatures over the last few decades, which has contributed to rising sea‐level. The oceans are also the main store of carbon dioxide (CO2), and are estimated to have taken up ∼40% of anthropogenic-sourced CO2 from the atmosphere since the beginning of the industrial revolution. A proportion of the carbon uptake is exported via the four ocean ‘carbon pumps’ (Solubility, Biological, Continental Shelf and Carbonate Counter) to the deep ocean reservoir. Increases in sea temperature and changing planktonic systems and ocean currents may lead to a reduction in the uptake of CO2 by the ocean; some evidence suggests a suppression of parts of the marine carbon sink is already underway. While the oceans have buffered climate change through the uptake of CO2 produced by fossil fuel burning this has already had an impact on ocean chemistry through ocean acidification and will continue to do so. Feedbacks to climate change from acidification may result from expected impacts on marine organisms (especially corals and calcareous plankton), ecosystems and biogeochemical cycles. The polar regions of the world are showing the most rapid responses to climate change. As a result of a strong ice–ocean influence, small changes in temperature, salinity and ice cover may trigger large and sudden changes in regional climate with potential downstream feedbacks to the climate of the rest of the world. A warming Arctic Ocean may lead to further releases of the potent greenhouse gas methane from hydrates and permafrost. The Southern Ocean plays a critical role in driving, modifying and regulating global climate change via the carbon cycle and through its impact on adjacent Antarctica. The Antarctic Peninsula has shown some of the most rapid rises in atmospheric and oceanic temperature in the world, with an associated retreat of the majority of glaciers. Parts of the West Antarctic ice sheet are deflating rapidly, very likely due to a change in the flux of oceanic heat to the undersides of the floating ice shelves. The final section on modelling feedbacks from the ocean to climate change identifies limitations and priorities for model development and associated observations. Considering the importance of the oceans to climate change and our limited understanding of climate-related ocean processes, our ability to measure the changes that are taking place are conspicuously inadequate. The chapter highlights the need for a comprehensive, adequately funded and globally extensive ocean observing system to be implemented and sustained as a high priority. Unless feedbacks from the oceans to climate change are adequately included in climate change models, it is possible that the mitigation actions needed to stabilise CO2 and limit temperature rise over the next century will be underestimated.

Swarming is a fundamental part of the life of Euphausia superba, yet we still know very little about what drives the considerable variability in swarm shape, size and biomass. We examined swarms across the Scotia Sea in January and February 2003 using a Simrad EK60 (38 and 120kHz) echosounder, concurrent with net sampling. The acoustic data were analysed through applying a swarm-identification algorithm and then filtering out all non-krill targets. The area, length, height, depth, packing-concentration and inter-swarm distance of 4525 swarms was derived by this method. Hierarchical clustering revealed 2 principal swarm types, which differed in both their dimensions and packing-concentrations. Type 1 swarms were generally small (<50m long) and were not very tightly packed (<10ind.m−3), whereas type 2 swarms were an order of magnitude larger and had packing concentrations up to 10 times greater. Further sub-divisions of these types identified small and standard swarms within the type 1 group and large and superswarms within the type 2 group. A minor group (swarm type 3) was also found, containing swarms that were isolated (>100km away from the next swarm). The distribution of swarm types over the survey grid was examined with respect to a number of potential explanatory variables describing both the environment and the internal-state of krill (namely maturity, body length, body condition). Most variables were spatially averaged over scales of ∼100km and so mainly had a mesoscale perspective. The exception was the level of light (photosynthetically active radiation (PAR)) for which measurements were specific to each swarm. A binary logistic model was constructed from four variables found to have significant explanatory power (P<0.05): surface fluorescence, PAR, krill maturity and krill body length. Larger (type 2) swarms were more commonly found during nighttime or when it was overcast during the day, when surface fluorescence was low, and when the krill were small and immature. A strong pattern of diel vertical migration was not observed although the larger and denser swarms tended to occur more often at night than during the day. The vast majority of krill were contained within a minor fraction of the total number of swarms. These krill-rich swarms were more common in areas dominated by small and immature krill. We propose that, at the mesoscale level, the structure of swarms switches from being predominantly large and tightly packed to smaller and more diffuse as krill grow and mature. This pattern is further modulated according to feeding conditions and then level of light.

The two polar regions have experienced remarkably different climatic changes in recent decades. The Arctic has seen a marked reduction in sea-ice extent throughout the year, with a peak during the autumn. A new record minimum extent occurred in 2007, which was 40% below the long-term climatological mean. In contrast, the extent of Antarctic sea ice has increased, with the greatest growth being in the autumn. There has been a large-scale warming across much of the Arctic, with a resultant loss of permafrost and a reduction in snow cover. The bulk of the Antarctic has experienced little change in surface temperature over the last 50 years, although a slight cooling has been evident around the coast of East Antarctica since about 1980, and recent research has pointed to a warming across West Antarctica. The exception is the Antarctic Peninsula, where there has been a winter (summer) season warming on the western (eastern) side. Many of the different changes observed between the two polar regions can be attributed to topographic factors and land/sea distribution. The location of the Arctic Ocean at high latitude, with the consequently high level of solar radiation received in summer, allows the icealbedo feedback mechanism to operate effectively. The Antarctic ozone hole has had a profound effect on the circulations of the high latitude ocean and atmosphere, isolating the continent and increasing the westerly winds over the Southern Ocean, especially during the summer and winter.

Species of the genus Pyramimonas (Prasinophyceae) are a common, widespread, but minor component of the Antarctic marine phytoplankton. They are often associated with the seasonal sea-ice environment. Pyramimonas gelidicola (McFadden, Moestrup & Wetherbee, 1982) was isolated from the water column of a saline Antarctic lake, and observations on the organism’s life history as it grew in unialgal cultures were made. The alga proved to be pleomorphic: capable of producing several morphologically distinct life stages. We recorded motile single-celled quadriflagellates that formed two statistically distinct size classes, a rare uniflagellate cell-type, and aggregations of quadriflagellate cells, multilobed forms and an encystment stage. Multilobed forms and cell aggregations, never before observed in an Antarctic Pyramimonas species, are presumed to be growth medium-induced morphotypes. Multilobed forms contained an equal number of nuclei and lobes, suggesting that they are the product of asexual reproduction. Some of the morphotypes we report here may never be observed under natural field conditions, but the potential for this alga to alternate between morphotypes is clearly demonstrated.

Snowmelt processes on Antarctic sea ice are examined. We present a simple snowmelt indicator based on diurnal brightness temperature variations from microwave satellite data. The method is validated through extensive field data from the western Weddell Sea and lends itself to the investigation of interannual and spatial variations of the typical snowmelt on Antarctic sea ice. We use in-situ measurements of physical snow properties to show that despite the absence of strong melting, the summer period is distinct from all other seasons with enhanced diurnal variations of snow wetness. A microwave emission model reveals that repeated thawing and refreezing cause the typical microwave emissivity signatures that are found on perennial Antarctic sea ice during summer. The proposed melt indicator accounts for the characteristic phenomenological stages of snowmelt in the Southern Ocean and detects the onset of diurnal snow wetting. An algorithm is presented to map large-scale snowmelt onset based on satellite data from the period between 1988 and 2006. The results indicate strong meridional gradients of snowmelt onset with the Weddell, Amundsen, and Ross Seas showing earliest (beginning of October) and most frequent snowmelt. Moreover, a distinct interannual variability of melt onset dates and large areas of first-year ice where no diurnal freeze thawing occurs at the surface are determined.

The vertical distribution (0–550 m) of zooplankton biomass, and indices of respiration (electron transfer system [ETS]) and structural growth (aminoacyltRNA synthetases activity [AARS]), were studied in waters off the Antarctic Peninsula during the austral summer of 2000. The dominant species were the copepod Metridia gerlachei and the euphausiid Euphausia superba. We observed a vertical krill/copepod substitution in the water column. The zooplankton biomass in the layer at a depth of 200–500 m was of the same magnitude as the biomass in the layer at a depth of 0–200 m, indicating that biomass in the mesopelagic zone is an important fraction of the total zooplankton in Antarctic waters. The metabolic rates of the zooplankton community were sustained by less than 0.5% of the primary production in the area, suggesting that microplankton or small copepods are the main food source. Neither food availability nor predation seemed to control mesozooplankton biomass. The wide time lag between the abundance peak of the dominant copepod (M. gerlachei) and the phytoplankton bloom is suggested to be the main explanation for the low summer zooplankton biomass observed in these waters.

A baseline for persistent organohalogen compound (POC) accumulation in the Antarctic keystone species, Antarctic krill (Euphausia superba) has been established for a 50° longitudinal range of the eastern Antarctic sector. Samples of adult krill, caught from 12 sites distributed between 30° and 80°E (60–70°S), were analysed for >100 organohalogen compounds including chlorinated pesticides, polychlorinated biphenyls (PCBs), polybrominated organic compounds and polychlorinated dibenzo-p-dioxins/furans (PCDD/Fs). Organochlorine pesticides dominated measured krill contaminant burdens with hexachlorobenzene (HCB) as the single most abundant compound quantified. Krill HCB concentrations were comparable to those detected at this trophic level in both the Arctic and temperate northwest Atlantic, lending support for the hypothesis that HCB will approach global equilibrium at a faster rate than other POCs. Para, para′-dichlorodiphenylethene (p,p′-DDE) was detected at notable concentrations. Measurements of DDT and its degradation products provide an important baseline for monitoring the temporal and geographical influence of renewed, DDT usage for malaria-control in affected southern hemisphere countries. In contrast to the Arctic, PCBs did not feature prominently in contaminant burdens of Antarctic krill. The major commercial polybrominated diphenyl ether (PBDE) congeners -99 and -47 were quantified at low background levels with clear concentration spikes observed at around 70°E , in the vicinity of modern, active research stations. The likelihood that local anthropogenic activities are supplementing low PBDE levels, delivered otherwise primarily via long range environmental transport, is discussed. The suspected naturally occurring brominated organic compound, 2,4,6-tribromoanisole (TBA), was a ubiquitous contaminant in all samples whereas the only PCDD/Fs quantifiable were trace levels of octachlorodibenzo-p-dioxin (OCDD) and 1,2,3,4,7,8/1,2,3,4,7,9-hexachlorodibenzofuran (HxCDF). With the aims of; i) Generating a robust and broadly applicable POC auditing platform for the scarcely studied eastern Antarctic sector; ii) Determining the compounds accumulating in Antarctic krill for further toxicity evaluation studies and iii) Establishing a baseline for Antarctic predator exposure to POCs, this study represents one of the most comprehensive reports of POC contamination of the Antarctic food web to date.

Polar regions are particularly sensitive to climate change, with the potential for significant feedbacks between ocean circulation, sea ice, and the ocean carbon cycle. However, the difficulty in obtaining in situ data means that our ability to detect and interpret change is very limited, especially in the Southern Ocean, where the ocean beneath the sea ice remains almost entirely unobserved and the rate of sea-ice formation is poorly known. Here, we show that southern elephant seals (Mirounga leonina) equipped with oceanographic sensors can measure ocean structure and water mass changes in regions and seasons rarely observed with traditional oceanographic platforms. In particular, seals provided a 30-fold increase in hydrographic profiles from the sea-ice zone, allowing the major fronts to be mapped south of 60°S and sea-ice formation rates to be inferred from changes in upper ocean salinity. Sea-ice production rates peaked in early winter (April?May) during the rapid northward expansion of the pack ice and declined by a factor of 2 to 3 between May and August, in agreement with a three-dimensional coupled ocean?sea-ice model. By measuring the high-latitude ocean during winter, elephant seals fill a ?blind spot? in our sampling coverage, enabling the establishment of a truly global ocean-observing system.

Investigations into Fe(II) cycling during two Southern Ocean mesoscale iron enrichment experiments, SOFeX and EIFeX, clearly show the importance of Fe(II) to iron speciation during these experiments. In both cases the added Fe(II) persisted significantly longer than its expected oxidation time indicating a significant Fe reduction process at work. During EIFeX diel studies showed a strong photochemically induced cycle in Fe(II) production in sunlit surface waters. Our results suggest that the photochemical cycling of iron may also be important in unfertilized waters of the Southern Ocean.

We present the first detailed maps of fast ice around East Antarctica (75°E–170°E), using an image correlation technique applied to RADARSAT ScanSAR images from November in 1997 and 1999. This method is based upon searching for, and distinguishing, correlated regions of the ice-covered ocean which remain stationary, in contrast to adjacent moving pack ice. Within the overlapping longitudinal range of ∼86°E–150.6°E, the total fast-ice area is 141,450 km2 in 1997 and 152,216 km2 in 1999. Calibrated radar backscatter data are also used to determine the distribution of two fast-ice classes based on their surface roughness characteristics. These are “smooth” fast ice (−25.4 dB to −13.5 dB) and “rough” fast ice (−13.5 dB to −2.5 dB). The former comprises ∼67% of the total area, with rough fast ice making up the remaining ∼33%. An estimate is made of fast-ice volume, on the basis of fast-ice type as a proxy measure of ice thickness and area. Results suggest that although fast ice forms 2–16% of the total November sea ice area for this sector of East Antarctica in 1997 and 1999 (average 8.3% across maps), it may comprise 6–57% of the total ice volume (average ∼28% across maps). Grounded icebergs play a key role in fast-ice distribution in all regions apart from 150°E–170°E. These are “snapshot” estimates only, and more work is required to determine longer-term spatiotemporal variability.

The annual trend in energy storage in the Antarctic minke whale was examined using catch data from all 18 survey years in the Japanese Whale Research Program (JARPA). Regression analyses clearly showed that blubber thickness, girth and fat weight have been decreasing for nearly 2 decades. The decrease per year is estimated at approximately 0.02 cm for mid-lateral blubber thickness and 17 kg for fat weight, corresponding to 9% for both measurements over the 18-year period. Furthermore, "date", "extent of diatom adhesion", "sex", "body length", "fetus length", "latitude", "age" and "longitude" were all identified as partially independent predictors of blubber thickness. The direct interpretation of this substantial decline in energy storage in terms of food availability is difficult, since no long-term krill abundance series is available. However, an increase in the abundance of krill feeders other than minke whales and a resulting decrease in the krill population must be considered as a likely explanation.