A Shift in the Biogenic Silica of Sediment in the Larsen B Continental Shelf,Off the Eastern Antarctic Peninsula,Resulting from Climate Change

In 2002, section B of the Larsen ice shelf, off of the Eastern Antarctic Peninsula, collapsed and created the opportunity to study whether the changes at the sea surface left evidence in the sedimentary record. Biogenic silica is major constituent of Antarctic marine sediment, and its presence in the sediment column is associated with diatom production in the euphotic zone. The abundance of diatom valves and the number of sponge spicules in the biogenic silica was analyzed to determine how the origin of the biogenic silica in the upper layers of the sediment column responded to recent environmental changes. Diatom valves were present only in the upper 2 cm of sediment, which roughly corresponds to the period after the collapse of the ice shelf. In contrast, sponge spicules, a more robust form of biogenic silica, were also found below the upper 2 cm layer of the sediment column. Our results indicate that in this region most of the biogenic silica in the sedimentary record originated from sponge spicules rather than diatoms during the time when the sea surface was covered by the Larsen ice shelf. Since the collapse of the ice shelf, the development of phytoplankton blooms and the consequent influx of diatom debris to the seabed have shifted the biogenic silica record to one dominated by diatom debris, as occurs in most of the Antarctic marine sediment. This shift provides further evidence of the anthropogenic changes to the benthic habitats of the Antarctic and will improve the interpretation of the sedimentary record in Polar Regions where these events occur.     

Utility of amino acids as biomarkers in polar marine sediments: a study on the continental shelf of Larsen region, Eastern Antarctic Peninsula

Ongoing global warming is affecting the polar regions at a faster pace than in many other lower latitude environments. Based on the idea that the changes at the sea surface leave a signal in the sedimentary record, we analysed the total hydrolysable amino acid (THAA) and enzymatically hydrolysable amino acid (EHAA) contents in sediments off the coast of the eastern Antarctic Peninsula during the decade following the collapse of sections A and B of the Larsen ice shelf to check their utility as biomarkers of this event. Two organic matter lability indexes (the EHAA-to-THAA ratio and the Dauwe degradation index) were also calculated to assess the quality of the organic matter in the sediment column. The THAA and EHAA concentrations in the upper 5 mm varied between ~1 and ~10 nmol mg^?1 DW^?1, corresponding to an oligotrophic environment, whereas the quality of the organic matter as indicated by the lability indexes was relatively high in the upper sediment column (<2 cm deep). The amino acid profiles and indexes in the sediment column were compared to the pigment profiles and indexes published in previous studies for the same stations. The results suggest that in the sediment column, pigments track more accurately than amino acids the pelagic organic matter supply to the seabed after the collapse of the Larsen ice shelf.     

The diversity,abundance and fate of ice algae and phytoplankton in the Bering Sea

Despite being an essential part of the marine food web during periods of ice cover, sea ice algae have not been studied in any detail in the Bering Sea. In this study, we investigated the diversity, abundance and ultimate fate of ice algae in the Bering Sea using sea ice, water and sub-ice sediment trap samples collected during two spring periods in 2008 and 2009: ice growth (March–mid-April) and ice melt (mid-April–May). The total ice algal species inventory included 68 species, dominated by typical Arctic ice algal diatom taxa. Only three species were determined from the water samples; we interpret the strong overlap in species as seeding of algal cells from the sea ice. Algal abundances in the ice exceeded 10⁷ cells l^?1 in the bottom 2-cm layer and were on average three orders of magnitude higher than in the water column. The vertical flux of algal cells beneath the ice during the period of ice melt (>10⁸ cells m^?2 day^?1) exceeded export during the ice growth period by one order of magnitude; the vertical flux during both periods can only be sustained by the release of algae from the ice. Differences in the relative species proportions of algae among sample types indicated that the fate of the released ice algae was species specific, with some taxa contributing to seeding in the water column, while other taxa were preferentially exported.     

Spatial and temporal variability in export fluxes of biogenic matter in Kongsfjorden

The marine ecosystem of Kongsfjorden experiences large variations in primary productivity due to pronounced seasonal variations in sunlight, glacier melt, and ice cover. The objective of this study was to assess spatial and seasonal variability in the downward export of biogenic matter in Kongsfjorden. Short-term sediment traps were deployed for periods ranging from 21 to 52 h at three stations from the inner fjord to the outer fjord in May, August, and October 2012 and at one mid-fjord station in January 2013. Total particulate matter, particulate organic carbon, phytoplankton cells, chlorophyll a, biogenic particulate silica, and zooplankton fecal pellet fluxes were measured to determine the magnitude and composition of the material exported in the fjord. The amount and composition of export fluxes reflected a large phytoplankton bloom grazed upon by zooplankton in May, the melting of glaciers and the intrusion of Atlantic Water in August, the end of the glacier melt period in October, and the polar night in January. Overall, seasonal changes in the phytoplankton community impacted export efficiency in the fjord, directly through phytoplankton sinking and indirectly through zooplankton grazing. Results obtained in this study may reflect the magnitude and composition of export fluxes to expect in coming years in Kongsfjorden, especially under conditions of warmer Atlantic Water and longer glacier melt periods.     

Inter-annual variability in the proportional contribution of higher trophic levels to the diet of Pacific walruses

Pacific walruses (Odobenus rosmarus divergens) depend on Arctic sea ice as a resting and foraging platform; however, recent years have seen unprecedented seasonal reductions in ice extent. Previous researchers proposed that during unfavorable ice conditions, walruses might prey on other pinnipeds. To examine this hypothesis, we analyzed carbon and nitrogen stable isotope ratios of muscle from walruses (n = 155) sampled from the Bering and Chukchi seas during 2001–2010. We used a Bayesian stable isotope mixing model to examine the proportional contribution of higher trophic level prey (HTLP) (e.g., seals, seabirds) to walrus diets and extrapolated a tissue-specific turnover rate to compare diet of individuals over time. Mode HTLP across years was 19 % ± 8. Results indicate a significant decrease (P < 0.05) in the reliance on HTLP during 2008–2009 (mode HTLP 13 %), one of two sampling periods that experienced great seasonal loss of pan-Arctic sea ice (the other being 2007–2008 with mode HTLP of 23 %). We also reveal intra-annual fluctuations in the contribution of HTLP to the diet of a walrus sampled in 2011 with seal remains in its stomach through high-resolution sectioning along a whisker length. Our findings suggest that walruses forage opportunistically as a result of multiple environmental factors and that sea ice extent alone does not drive consumption of HTLP.     

Ecology of sea ice biota

Summary The sea ice does not only determine the ecology of ice biota, but it also influences the pelagic systems under the ice cover and at ice edges. In this paper, new estimates of Arctic and Antarctic production of biogenic carbon are derived, and differences as well as similarities between the two oceans are examined. In ice-covered seas, high algal concentrations (blooms) occur in association with several types of conditions. Blooms often lead to high sedimentation of intact cells and faecal pellets. In addition to ice-related blooms, there is progressive accumulation of organic matter in Arctic multi-year ice, whose fate may potentially be similar to that of blooms. A fraction of the carbon fixed by microalgae that grow in sea ice or in relation to it is exported out of the production zone. This includes particulate material sinking out of the euphotic zone, and also material passed on to the food web. Pathways through which ice algal production does reach various components of the pelagic and benthic food webs, and through them such top predators as marine mammals and birds, are discussed. Concerning global climate change and biogeochemical fluxes of carbon, not all export pathways from the euphotic zone result in the sequestration of carbon for periods of hundreds of years or more. This is because various processes, that take place in both the ice and the water column, contribute to mineralize organic carbon into CO₂ before it becomes sequestered. Processes that favour the production and accumulation of biogenic carbon as well as its export to deep waters and sequestration are discussed, together with those that influence mineralization in the upper ice-covered ocean.Authors are members of SCOR Working Group 86: Ecology of Sea Ice Biota     

Fatty acid and stable isotope characteristics of sea ice and pelagic particulate organic matter in the Bering Sea: tools for estimating sea ice algal contribution to Arctic food web production

We determined fatty acid (FA) profiles and carbon stable isotopic composition of individual FAs (δ¹³C_FA values) from sea ice particulate organic matter (i-POM) and pelagic POM (p-POM) in the Bering Sea during maximum ice extent, ice melt, and ice-free conditions in 2010. Based on FA biomarkers, differences in relative composition of diatoms, dinoflagellates, and bacteria were inferred for i-POM versus p-POM and for seasonal succession stages in p-POM. Proportions of diatom markers were higher in i-POM (16:4n-1, 6.6–8.7 %; 20:5n-3, 19.6–25.9 %) than in p-POM (16:4n-1, 1.2–4.0 %; 20:5n-3, 5.5–14.0 %). The dinoflagellate marker 22:6n-3/20:5n-3 was highest in p-POM. Bacterial FA concentration was higher in the bottom 1 cm of sea ice (14–245 μg L^?1) than in the water column (0.6–1.7 μg L^?1). Many i-POM δ¹³C_FA values were higher (up to ~10 ‰) than those of p-POM, and i-POM δ¹³C_FA values increased with day length. The higher i-POM δ¹³C_FA values are most likely related to the reduced dissolved inorganic carbon (DIC) availability within the semi-closed sea ice brine channel system. Based on a modified Rayleigh equation, the fraction of sea ice DIC fixed in i-POM ranged from 12 to 73 %, implying that carbon was not limiting for primary productivity in the sympagic habitat. These differences in FA composition and δ¹³C_FA values between i-POM and p-POM will aid efforts to track the proportional contribution of sea ice algal carbon to higher trophic levels in the Bering Sea and likely other Arctic seas.     

Year-round acoustic detection of bearded seals (Erignathus barbatus) in the Beaufort Sea relative to changing environmental conditions, 2008–2010

Bearded seals (Erignathus barbatus) are pan-Arctic pinnipeds that are often seen in association with pack ice, and are known for their long, loud trills, produced underwater primarily in the spring. Acoustic recordings were collected from August 2008 to August 2010 at two locations and a single year (2008–2009) at a third location, in the western Beaufort Sea. Three recorders in 2008–2009 had a 30 % duty cycle and a bandwidth of 10–4,096 Hz. One recorder in 2009–2010 had a 45 % duty cycle and a bandwidth of 10–4,096 Hz and the second had a 20 % duty cycle and bandwidth of 10–8,192 Hz. Spectrograms of acoustic data were examined for characteristic patterns of bearded seal vocalizations. For each recorder, the number of hours per day with vocalizations was compared with in situ water temperature and satellite-derived daily sea ice concentrations. At all sites, bearded seals were vocally active year-round. Call activity escalated with the formation of pack ice in the winter and the peak occurred in the spring, coinciding with mating season and preceding breakup of the sea ice. There was a change in the timing of seasonal sea ice formation and retreat between the two consecutive years that was reflected in the timing of peak bearded seal call activity. This study provides new information on fall and winter bearded seal vocal behavior and the relationship between year-round vocal activity and changes in annual sea ice coverage and in situ water temperature.     

Size and stage composition of age class 0 Antarctic krill (<Emphasis Type="Italic">Euphausia superba</Emphasis>) in the ice–water interface layer during winter/early spring

The condition and survival of Antarctic krill (Euphausia superba) strongly depends on sea ice conditions during winter. How krill utilize sea ice depends on several factors such as region and developmental stage. A comprehensive understanding of sea ice habitat use by krill, however, remains largely unknown. The aim of this study was to improve the understanding of the krill’s interaction with the sea ice habitat during winter/early spring by conducting large-scale sampling of the ice–water interface (0–2 m) and comparing the size and developmental stage composition of krill with the pelagic population (0–500 m). Results show that the population in the northern Weddell Sea consisted mainly of krill that were <1 year old (age class 0; AC0), and that it was comprised of multiple cohorts. Size per developmental stage differed spatially, indicating that the krill likely were advected from various origins. The size distribution of krill differed between the two depth strata sampled. Larval stages with a relatively small size (mean 7–8 mm) dominated the upper two metre layer of the water column, while larger larvae and AC0 juveniles (mean 14–15 mm) were proportionally more abundant in the 0- to 500-m stratum. Our results show that, as krill mature, their vertical distribution and utilization of the sea ice appear to change gradually. This could be the result of changes in physiology and/or behaviour, as, e.g., the krill’s energy demand and swimming capacity increase with size and age. The degree of sea ice association will have an effect on large-scale spatial distribution patterns of AC0 krill and on predictions of the consequences of sea ice decline on their survival over winter.     

High variability in iron-bound organic carbon among five boreal lake sediments

Being both stable carbon sinks and greenhouse gas sources, boreal lake sediments represent significant players in carbon (C) cycling. The release of dissolved organic carbon (DOC) into anoxic water is a widespread phenomenon in boreal lakes with impact on sediment C budgets. The association of OC with iron (Fe) is assumed to play an important role for this anoxic OC release via the dissimilatory reduction of Fe, but also to influence the stabilization of OC in sediments. To investigate the role of Fe–OC association for OC dynamics in different boreal lake sediments, we compared the content of Fe-bound OC [Fe–OC, defined as citrate bicarbonate dithionite (CBD) extractable OC] and the extent of reductive dissolution of solid-phase Fe and OC at anoxia. We found high among-lake variability in Fe–OC content, and while the amount of Fe–OC was high in three of the lakes (980–1920 µmol g^?1), the overall contribution of Fe–OC to the sediment OC pool in all study lakes was not higher than 11%. No linkages between the amount of the Fe–OC pool and lake or sediment characteristics (e.g., pH, DOC concentration, sediment OC content, C:N ratio) could be identified. The observed release of OC from anoxic sediment may be derived from dissolution of Fe–OC in the lake sediments with high Fe–OC, but in other lake sediments, OC release during anoxia exceeded the sediment Fe–OC pool, indicating low contribution of reductive Fe dissolution to OC release from these lake sediments. The range of the investigated boreal lakes reflects the high variability in the size of the sediment Fe–OC pool (0–1920 µmol g^?1) and CBD-extractable Fe (123–4050 µmol g^?1), which was not mirrored in the extent of reductive dissolution of Fe (18.9–84.6 µmol g^?1) and OC (1080–1700 µmol g^?1) during anoxia, suggesting that Fe-bound OC may play a minor role for sediment OC release in boreal lakes. However, studies of redox-related OC cycling in boreal lake sediments should consider that the amount of Fe–OC can be high in some lakes.     

Late pleistocene paleoclimates of the South Pacific based on statistical analysis of planktonic foraminifers

Statistical analysis applied to foraminiferal data from 78 South Pacific core tops enables the derivation of a transfer function that relates sea surface temperature to foraminiferal assemblages. Application of this transfer function to eight cores from the southern part of the East Pacific Rise yields estimates of the sea surface temperatures of the last glacial maximum, as well as the paleotemperature record of the past 150,000 years. Comparison of the last glacial temperature estimates with the recent sea surface temperature shows that the greatest change between glacial and present conditions (about 5°C) occurs in a climatically sensitive area near 50°S. Stratigraphic correlation of two cores from this area suggests that the last glacial started in this area with rapid cooling, and that the climate stayed generally cold until the end of the glacial. Similar general shape of the climatic record is found in the high latitudes of the North Atlantic as well as in the ice sheets of Greenland and Antarctica. In contrast to the similarity in the shape of these high-latitude records, they differ distinctly from the foraminiferal oxygen isotope record of several deep-sea cores which indicates a general gradual increase of ice volume from the beginning of the last glacial to the maximum glaciation which occurred about 18,000 years B.P.In the study area the rate of sediment accumulation during the last glacial is about two to three times less than in the last interglacial. There is no indication of increased carbonate solution during the glacial, and it is suggested that the change in the accumulation rate results from a reduction in the supply of calcareous shells to the sediment. It seems that with cooling, the environment becomes less favorable to organisms producing calcium carbonate tests, and therefore carbonate production decreases during the glacial.     

Sea ice meiofauna distribution on local to pan‐Arctic scales

Arctic sea ice provides microhabitats for biota that inhabit the liquid‐filled network of brine channels and the ice–water interface. We used meta‐analysis of 23 published and unpublished datasets comprising 721 ice cores to synthesize the variability in composition and abundance of sea ice meiofauna at spatial scales ranging from within a single ice core to pan‐Arctic and seasonal scales. Two‐thirds of meiofauna individuals occurred in the bottom 10 cm of the ice. Locally, replicate cores taken within meters of each other were broadly similar in meiofauna composition and abundance, while those a few km apart varied more; 75% of variation was explained by station. At the regional scale (Bering Sea first‐year ice), meiofauna abundance varied over two orders of magnitude. At the pan‐Arctic scale, the same phyla were found across the region, with taxa that have resting stages or tolerance to extreme conditions (e.g., nematodes and rotifers) dominating abundances. Meroplankton, however, was restricted to nearshore locations and landfast sea ice. Light availability, ice thickness, and distance from land were significant predictor variables for community composition on different scales. On a seasonal scale, abundances varied broadly for all taxa and in relation to the annual ice algal bloom cycle in both landfast and pack ice. Documentation of ice biota composition, abundance, and natural variability is critical for evaluating responses to decline in Arctic sea ice. Consistent methodology and protocols must be established for comparability of meiofauna monitoring across the Arctic. We recommend to (1) increase taxonomic resolution of sea ice meiofauna, (2) focus sampling on times of peak abundance when seasonal sampling is impossible, (3) include the bottom 30 cm of ice cores rather than only bottom 10 cm, (4) preserve specimens for molecular analysis to improve taxonomic resolution, and (5) formulate a trait‐based framework that relates to ecosystem functioning.     

Milk fatty acid profile of Peruvian Criollo and Brown Swiss cows in response to different diet qualities fed at low and high altitude

Two identical experimental protocols were followed at 200 and 3,600 m above sea level (a.s.l.) determining the changes of the milk fatty acid (FA) profile of Brown Swiss (BS) and indigenous Peruvian Criollo cows (CR) as a response to diets which were designed to cover the variation in feed quality caused by season. At each site (altitude), six BS and six CR cows, adapted to >3,500 m a.s.l., were fed three dietary treatments (DS, dry-season forage; RS rainy-season forage; OC, diet optimised to meet the cow's requirements) in a 2 × 2 × 3-factorial arrangement. Intakes of FA and milk yield increased from diet DS (low quality diet) to RS and OC (high quality diet) for both cow types. Milk fat proportions of conjugated linoleic acid (CLA), C18:3 c9,c12,c15, total n-3 and polyunsaturated FA (PUFA) were highest (p < 0.05) with diet OC and higher in the lowlands than in the highlands. Low intakes of diet DS obviously resulted in a ruminal energy deficiency and body lipid mobilisation. The ruminal energy deficiency with diet DS was especially pronounced in BS, apparently reducing biohydrogenation rate and leading to lower proportions of C18:0 and higher proportions of C18:3 c9,c12,c15 in milk fat (p < 0.05). Especially C18:3 c9,c12,c15 intake did not concur with its proportion in milk fat, suggesting a strong dependence on energy status. Milk yield and FA excretion with milk were higher for BS than for CR (p < 0.05) with all three diets although milk fat content was lower (p < 0.05) for BS than CR. Milk fat of BS was richer in CLA and PUFA than milk fat of CR (p < 0.05). The desaturase indices for 18 FA were also higher for BS than CR (p < 0.05), suggesting a slightly higher Δ9-desaturase activity for BS, especially with diet DS. Milk fat content was generally higher at the high altitude than at the lowland site (p < 0.05), whereas the FA profile was unexpectedly similar across sites. Various interactions were found among diet type, cow type and altitude (site) indicating that a combination of these factors contributes to the characteristic FA profile of the respective milk.     

Nitrification contributes to winter oxygen depletion in seasonally frozen forested lakes

In lakes that experience seasonal ice cover, understanding of nitrogen–oxygen coupling and nitrification has been dominated by observations during open water, ice-free conditions. To address knowledge gaps about nitrogen–oxygen linkages under ice, we examined long-term winter data (30 + years, 2–3 sample events per winter) in 7 temperate lakes of forested northern Wisconsin, USA. Across lakes and depths, there were strong negative relationships between dissolved oxygen (DO) and the number of days since ice-on, reflecting consistent DO consumption rates under ice. In two bog lakes that routinely experience prolonged winter DO concentrations below 1.0 mg L^?1, nitrate accumulated near the ice surface mainly in late winter, suggesting nitrification may depend on biogenic oxygen from photosynthesis. In contrast, within five oligotrophic-mesotrophic lakes, nitrate accumulated more consistently over winter and often throughout the water column, especially at intermediate depths. Exogenous inputs of nitrate to these lakes were minimal compared to rates of nitrate accumulation. To produce the nitrate via in-lake nitrification, substantial oxygen consumption by ammonium oxidizing microbes would be required. Among lakes and depths that had significant DO depletion over winter, the stoichiometric nitrifier oxygen demand ranged from 1 to 25% of the DO depletion rate. These estimates of nitrifier-driven DO decline are likely conservative because we did not account for nitrate consumed by algal uptake or denitrification. Our results provide an example of nitrification at temperatures < 5 degrees C having a substantial influence on ecosystem-level nitrogen and oxygen availability in seasonally-frozen, northern forested lakes. Consequently, models of under-ice dissolved oxygen dynamics may be advanced through consideration of nitrification, and more broadly, coupled nitrogen and oxygen cycling.     

The relative contributions of biological and abiotic processes to carbon dynamics in subarctic sea ice

Knowledge on the relative effects of biological activity and precipitation/dissolution of calcium carbonate (CaCO₃) in influencing the air-ice CO₂ exchange in sea-ice-covered season is currently lacking. Furthermore, the spatial and temporal occurrence of CaCO₃ and other biogeochemical parameters in sea ice are still not well described. Here we investigated autotrophic and heterotrophic activity as well as the precipitation/dissolution of CaCO₃ in subarctic sea ice in South West Greenland. Integrated over the entire ice season (71 days), the sea ice was net autotrophic with a net carbon fixation of 56 mg C m^?2, derived from a sea-ice-related gross primary production of 153 mg C m^?2 and a bacterial carbon demand of 97 mg C m^?2. Primary production contributed only marginally to the TCO₂ depletion of the sea ice (7–25 %), which was mainly controlled by physical export by brine drainage and CaCO₃ precipitation. The net biological production could only explain 4 % of this sea-ice-driven CO₂ uptake. Abiotic processes contributed to an air-sea CO₂ uptake of 1.5 mmol m^?2 sea ice day^?1, and dissolution of CaCO₃ increased the air-sea CO₂ uptake by 36 % compared to a theoretical estimate of melting CaCO₃-free sea ice. There was a considerable spatial and temporal variability of CaCO₃ and the other biogeochemical parameters measured (dissolved organic and inorganic nutrients).     

Late Quaternary environmental and climate history of Rauer Group, East Antarctica

The Rauer Group is an archipelago in Prydz Bay, East Antarctica. The ice-free islands and the surrounding shallow marine areas provide valuable archives for the reconstruction of the late Pleistocene and Holocene environmental and climatic history of the region. Two sediment records from two marine inlets of Rauer Group have been studied for their sedimentological, geochemical, and biological characteristics. Radiocarbon ages from one of the inlets indicate ice-free conditions within the last glacial cycle, probably during the second half of Marine Isotope Stage 3. Subsequent ice sheet coverage of Rauer Group during the Last Glacial Maxiumum (LGM) can be inferred from a till layer recovered in one of the basins. The inlets became ice-free prior to 11,200 cal yr BP, when biogenic sedimentation started. Deglacial processes in the catchments, however, influenced the inlets until ~ 9200 cal yr BP as evidenced by the input of minerogenic material. Marine productivity under relatively open water conditions indicates an early Holocene climate optimum until 8200 cal yr BP, which is followed by a cooler period with increased sea ice. Warmer conditions are inferred for the mid Holocene, when both basins experienced an input of freshwater between ~ 5700-3500 cal yr BP, probably due to ice-sheet melting and increased precipitation on the islands. Neoglacial cooling in the late Holocene since c. 3500 cal yr BP is reflected by an increase in sea ice in both inlets.     

Carbon Sequestration in a Large Hydroelectric Reservoir: An Integrative Seismic Approach

Artificial reservoirs likely accumulate more carbon than natural lakes due to their unusually high sedimentation rates. Nevertheless, the actual magnitude of carbon accumulating in reservoirs is poorly known due to a lack of whole-system studies of carbon burial. We determined the organic carbon (OC) burial rate and the total OC stock in the sediments of a tropical hydroelectric reservoir by combining a seismic survey with sediment core sampling. Our data suggest that no sediment accumulation occurs along the margins of the reservoir and that irregular bottom morphology leads to irregular sediment deposition. Such heterogeneous sedimentation resulted in high spatial variation in OC burial—from 0 to 209 g C m^?2 y^?1. Based on a regression between sediment accumulation and OC burial rates (R ² = 0.94), and on the mean reservoir sediment accumulation rate (0.51 cm y^?1, from the seismic survey), the whole-reservoir OC burial rate was estimated at 42.2 g C m^?2 y^?1. This rate was equivalent to 70% of the reported carbon emissions from the reservoir surface to the atmosphere and corresponded to a total sediment OC accumulation of 0.62 Tg C since the reservoir was created. The approach we propose here allows an inexpensive and integrative assessment of OC burial in reservoirs by taking into account the high degree of spatial variability and based on a single assessment. Because burial can be assessed shortly after the survey, the approach combining a seismic survey and coring could, if applied on a larger scale, contribute to a more complete estimate of carbon stocks in freshwater systems in a relatively short period of time.     

An extreme wandering leopard seal, <Emphasis Type="Italic">Hydrurga leptonyx</Emphasis>, at Pitcairn Island,central South Pacific

Leopard seals are distributed around the Antarctic continent principally between 50°S and 80°S though they are known to wander even farther north, particularly to Australia, New Zealand, South America, and South Africa, and several sub-Antarctic Islands. Seasonal movements of leopard seals have been correlated with seasonal changes in the distribution of sea ice with seals moving north as sea ice develops in spring and winter and southward toward the Antarctic continent as it melts in late autumn and winter. On August 9, 2013, an emaciated juvenile male leopard seal was observed swimming in Bounty Bay at Pitcairn Island (25°4′S, 130°6′W). It was found ashore at a boat ramp in the bay the next day. Because of the seal’s apparent distress, it was promptly shot and killed humanely by an island police officer and then dumped at sea before any measurements or additional observations could be made. We estimated the seal to be a 10-month-old pup, about 1.8–2 m long. The appearance of this leopard seal at Pitcairn Island is only slightly farther south than the most northern record (the Cook Islands, 21°25′S, 159°8′W) for the species, but it is the most remote occurrence yet documented worldwide and correlates with the all-time record for sea ice coverage in the Antarctic in winter 2013.     

Distribution and abundance of the planktic foraminifer Neogloboquadrina pachyderma in sea ice of the Weddell Sea (Antarctica)

Summary Sea ice cores were obtained from eleven fast ice stations and one floe in the Weddell Sea, Antarctica in January–February 1985. All cores from the north eastern part of the Weddell Sea contained numerous living and dead planktic foraminifers of the species Neogloboquadrina pachyderma (Ehrenberg), while cores drilled in southern parts were barren of foraminifers with one exception. Foraminiferal abundances were variable, with numbers up to 320 individuals per liter melted sea ice. Distribution of foraminifers appears to be patchy, parallel cores taken less than 30 cm apart contained numbers which varied considerably. On the other hand, three cores taken on a transect each more than 3 km apart showed striking similarities. In general, small dead tests were found in the upper parts of the sea ice cores while large living individuals mainly occurred in lower sections. Abundant diatoms probably serve as a food source for the foraminifers. Correlation of foraminiferal abundance with salinity, chlorophyll and nutrient profiles are inconsistent. The possible mechanism of incorporation of N. pachyderma into the ice is discussed.