55 research outputs found

    Dive Patterns of Belugas (Delphinapterus leucas) in Waters Near Eastern Devon Island

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    Data were obtained for six belugas or white whales (Delphinapterus leucas) instrumented with satellite-linked dive recorders in September-November 1995 in waters near eastern Devon Island, Canada. The mean of the daily maximum depths of dives was 483-665 m for the 31-51 days when maximum depth measurements were taken. The deepest dive recorded was 872 m. Both the dive rate (number of dives per hour to depths > 8 m) and the time at surface (time spent within the uppermost 5 m of the water column) declined from mid-September through mid-October. The four females had significantly elevated dive rates during the nights (2300-0500), whereas the males showed no effects of time of day on the dive rates. Few dives lasted more than 18 min, and most lasted either less than 1 min or for 9-18 min. A trend from short dives to longer dives was noted from mid-September through October, along with a decline in the number of dives to 8-20 m and a corresponding increase in the number of dives to 200-452 m during the same period. The small whales made more dives and had longer times at the surface than the large whales, but they did not dive as deeply or for as long periods as did the large whales. Vertical speeds ranged from .05 ms to .19 ms for depths of 52-800 m. These speeds are significantly faster than vertical speeds recorded from narwhals (Monodon monoceros).En septembre-novembre 1995, on a recueilli des données sur six bélugas ou dauphins blancs (Delphinapterus leucas) équipés d'enregistreurs de plongée en liaison avec un satellite, dans les eaux proches de la partie est de l'île Devon au Canada. La moyenne quotidienne de la profondeur maximale des plongées était de 483 à 665 m pour les 31 à 51 jours durant lesquels on a mesuré la profondeur maximale. La plongée la plus profonde enregistrée était de 872 m. De mi-septembre à mi-octobre, le taux de plongée (nombre de plongées par heure à des profondeurs > à 8 m), de même que le temps en surface (temps passé dans les 5 m supérieurs de la colonne d'eau) ont diminué. Les quatre femelles affichaient un taux de plongée nettement supérieur durant la nuit (de 23 h à 5 h), tandis que le taux de plongée des mâles n'était pas affecté par le moment de la journée. Peu de plongées duraient plus de 18 mn et la plupart duraient soit moins d'une minute, soit de 9 à 18 mn. De mi-septembre à fin octobre, on a noté une tendance à la hausse dans la durée des plongées, parallèlement à une baisse du nombre de plongées entre 8 et 20 m de profondeur et une augmentation correspondante du nombre de plongées entre 200 et 452 m au cours de la même période. Pour les petits dauphins blancs, le nombre de plongées et la durée des périodes passées en surface étaient plus grands que pour les gros dauphins. Les vitesses verticales allaient de 0,5 m/s à 1,9 m/s pour des profondeurs allant de 52 à 800 m. Ces vitesses sont notablement plus rapides que les vitesses verticales enregistrées pour les narvals (Monodon monoceros)

    Atlantic water variability on the SE Greenland continental shelf and its relationship to SST and bathymetry

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    Author Posting. © American Geophysical Union, 2013. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 118 (2013): 847–855, doi:10.1029/2012JC008354.Interaction of warm, Atlantic-origin water (AW) and colder, polar origin water (PW) advecting southward in the East Greenland Current (EGC) influences the heat content of water entering Greenland's outlet glacial fjords. Here we use depth and temperature data derived from deep-diving seals to map out water mass variability across the continental shelf and to augment existing bathymetric products. We compare depths derived from the seal dives with the IBCAO Version 3 bathymetric database over the shelf and find differences up to 300 m near several large submarine canyons. In the vertical temperature structure, we find two dominant modes: a cold mode, with the typical AW/PW layering observed in the EGC, and a warm mode, where AW is present throughout the water column. The prevalence of these modes varies seasonally and spatially across the continental shelf, implying distinct AW pathways. In addition, we find that satellite sea surface temperatures (SST) correlate significantly with temperatures in the upper 50 m (R = 0.54), but this correlation decreases with depth (R = 0.22 at 200 m), and becomes insignificant below 250 m. Thus, care must be taken in using SST as a proxy for heat content, as AW mainly resides in these deeper layers.Funding for this work came from National Science Foundation OPP grant 0909373 and OCE grant 1130008, plus the WHOI Arctic Research Initiative. The Greenland Institute of Natural Resources and the Department of Fisheries and Oceans, Canada, supported the seal tagging logistics.2013-08-2

    Do Organohalogen Contaminants Contribute to Histopathology in Liver from East Greenland Polar Bears (Ursus maritimus)?

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    In East Greenland polar bears (Ursus maritimus), anthropogenic organohalogen compounds (OHCs) (e.g., polychlorinated biphenyls, dichlorodiphenyltrichloroethane, and polybrominated diphenyl ethers) contributed to renal lesions and are believed to reduce bone mineral density. Because OHCs are also hepatotoxic, we investigated liver histology of 32 subadult, 24 adult female, and 23 adult male East Greenland polar bears sampled during 1999–2002. Light microscopic changes consisted of nuclear displacement from the normal central cytoplasmic location in parenchymal cells, mononuclear cell infiltrations (mainly portally and as lipid granulomas), mild bile duct proliferation accompanied by fibrosis, and fat accumulation in hepatocytes and pluripotent Ito cells. Lipid accumulation in Ito cells and bile duct hyperplasia accompanied by portal fibrosis were correlated to age, whereas no changes were associated with either sex or season (summer vs. winter). For adult females, hepatocytic intracellular fat increased significantly with concentrations of the sum of hexachlorocyclohexanes, as was the case for lipid granulomas and hexachlorobenzene in adult males. Based on these relationships and the nature of the chronic inflammation, we suggest that these findings were caused by aging and long-term exposure to OHCs. Therefore, these changes may be used as biomarkers for OHC exposure in wildlife and humans. To our knowledge, this is the first time liver histology has been evaluated in relation to OHC concentrations in a mammalian wildlife species, and the information is important to future polar bear conservation strategies and health assessments of humans relying on OHC-contaminated food resources

    Quantitative fatty acid signature analysis reveals a high level of dietary specialization in killer whales across the North Atlantic

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    Quantifying the diet composition of apex marine predators such as killer whales (Orcinus orca) is critical to assessing their food web impacts. Yet, with few exceptions, the feeding ecology of these apex predators remains poorly understood. Here, we use our newly validated quantitative fatty acid signature analysis (QFASA) approach on nearly 200 killer whales and over 900 potential prey to model their diets across the 5000 km span of the North Atlantic. Diet estimates show that killer whales mainly consume other whales in the western North Atlantic (Canadian Arctic, Eastern Canada), seals in the mid-North Atlantic (Greenland), and fish in the eastern North Atlantic (Iceland, Faroe Islands, Norway). Nonetheless, diet estimates also varied widely among individuals within most regions. This level of inter-individual feeding variation should be considered for future ecological studies focusing on killer whales in the North Atlantic and other oceans. These estimates reveal remarkable population- and individual-level variation in the trophic ecology of these killer whales, which can help to assess how their predation impacts community and ecosystem dynamics in changing North Atlantic marine ecosystems. This new approach provides researchers with an invaluable tool to study the feeding ecology of oceanic top predators

    Abundance and species diversity hotspots of tracked marine predators across the North American Arctic

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    Aim: Climate change is altering marine ecosystems worldwide and is most pronounced in the Arctic. Economic development is increasing leading to more disturbances and pressures on Arctic wildlife. Identifying areas that support higher levels of predator abundance and biodiversity is important for the implementation of targeted conservation measures across the Arctic. Location: Primarily Canadian Arctic marine waters but also parts of the United States, Greenland and Russia. Methods: We compiled the largest data set of existing telemetry data for marine predators in the North American Arctic consisting of 1,283 individuals from 21 species. Data were arranged into four species groups: (a) cetaceans and pinnipeds, (b) polar bears Ursus maritimus (c) seabirds, and (d) fishes to address the following objectives: (a) to identify abundance hotspots for each species group in the summer–autumn and winter–spring; (b) to identify species diversity hotspots across all species groups and extent of overlap with exclusive economic zones; and (c) to perform a gap analysis that assesses amount of overlap between species diversity hotspots with existing protected areas. Results: Abundance and species diversity hotpots during summer–autumn and winter–spring were identified in Baffin Bay, Davis Strait, Hudson Bay, Hudson Strait, Amundsen Gulf, and the Beaufort, Chukchi and Bering seas both within and across species groups. Abundance and species diversity hotpots occurred within the continental slope in summer–autumn and offshore in areas of moving pack ice in winter–spring. Gap analysis revealed that the current level of conservation protection that overlaps species diversity hotspots is low covering only 5% (77,498 km 2 ) in summer–autumn and 7% (83,202 km 2 ) in winter–spring. Main conclusions: We identified several areas of potential importance for Arctic marine predators that could provide policymakers with a starting point for conservation measures given the multitude of threats facing the Arctic. These results are relevant to multilevel and multinational governance to protect this vulnerable ecosystem in our rapidly changing world

    Rapid circulation of warm subtropical waters in a major glacial fjord in East Greenland

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    Author Posting. © The Authors, 2009. This is the author's version of the work. It is posted here by permission of Nature Publishing Group for personal use, not for redistribution. The definitive version was published in Nature Geoscience 3 (2010): 182-186, doi:10.1038/ngeo764.The recent rapid increase in mass loss from the Greenland Ice Sheet is primarily attributed to an acceleration of outlet glaciers. One possible cause is increased melting at the ice/ocean interface driven by the synchronous warming of subtropical waters offshore of Greenland. This hypothesis is largely untested, however, because of the lack of observations from Greenland’s glacial fjords and our limited understanding of their dynamics. Here, we present new ship-based and moored oceanographic data, collected in Sermilik Fjord, a large glacial fjord in East Greenland, showing that subtropical waters are present throughout the fjord and are continuously replenished via a wind-driven exchange with the shelf, where they occur year-round. The temperature and rapid renewal of these waters suggest that, at present, they drive enhanced submarine melting at the terminus. Key controls on the melting rate are the volume and properties of subtropical waters on the shelf and the patterns of the along-shore winds, suggesting the glaciers’ acceleration was triggered by a combination of atmospheric and oceanic changes. These measurements provide evidence of rapid advective pathway for the transmission of oceanic variability to the ice-sheet margins and highlight an important process that is missing from prognostic ice-sheet models.F.S. acknowledges support from WHOI’s Ocean and Climate Change Institute’s Arctic Research Initiative and from NSF OCE 0751896, and G.S.H and L.A.S from NASA’s Cryospheric Sciences Program. Funding for the hooded seal deployments was obtained from the International Governance and Atlantic Seal Research Program, Fisheries and Oceans, Canada, to G. B. S. and to the Greenland Institute of Natural Resources to A. R. A

    Gut evacuation rate and grazing impact of the krill Thysanoessa raschii and T. inermis

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    Gut evacuation rates and ingestion rates were measured for the krill Thysanoessa raschii and T. inermis in Godthåbsfjord, SW Greenland. Combined with biomass of the krill community, the grazing potential on phytoplankton along the fjord was estimated. Gut evacuation rates were 3.9 and 2.3 h−1 for T. raschii and T. inermis, respectively. Ingestion rates were 12.2 ± 7.5 µg C mg C−1 day−1 (n = 4) for T. inermis and 4.9 ± 3.2 µg C mg C−1 day−1 (n = 4) for T. raschii, corresponding to daily rations of 1.2 and 0.5 % body carbon day−1. Clearance experiments conducted in parallel to the gut evacuation experiment gave similar results for ingestion rates and daily rations. Krill biomass was highest in the central part of the fjord’s length, with T. raschii dominating. Community grazing rates from krill and copepods were comparable; however, their combined impact was low, estimated as <1 % of phytoplankton standing stock being removed per day during this late spring study

    The Effects of Climate Change on Harp Seals (Pagophilus groenlandicus)

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    Harp seals (Pagophilus groenlandicus) have evolved life history strategies to exploit seasonal sea ice as a breeding platform. As such, individuals are prepared to deal with fluctuations in the quantity and quality of ice in their breeding areas. It remains unclear, however, how shifts in climate may affect seal populations. The present study assesses the effects of climate change on harp seals through three linked analyses. First, we tested the effects of short-term climate variability on young-of-the year harp seal mortality using a linear regression of sea ice cover in the Gulf of St. Lawrence against stranding rates of dead harp seals in the region during 1992 to 2010. A similar regression of stranding rates and North Atlantic Oscillation (NAO) index values was also conducted. These analyses revealed negative correlations between both ice cover and NAO conditions and seal mortality, indicating that lighter ice cover and lower NAO values result in higher mortality. A retrospective cross-correlation analysis of NAO conditions and sea ice cover from 1978 to 2011 revealed that NAO-related changes in sea ice may have contributed to the depletion of seals on the east coast of Canada during 1950 to 1972, and to their recovery during 1973 to 2000. This historical retrospective also reveals opposite links between neonatal mortality in harp seals in the Northeast Atlantic and NAO phase. Finally, an assessment of the long-term trends in sea ice cover in the breeding regions of harp seals across the entire North Atlantic during 1979 through 2011 using multiple linear regression models and mixed effects linear regression models revealed that sea ice cover in all harp seal breeding regions has been declining by as much as 6 percent per decade over the time series of available satellite data

    Are liver and renal lesions in East Greenland polar bears (Ursus maritimus) associated with high mercury levels?

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    BACKGROUND: In the Arctic, polar bears (Ursus maritimus) bio-accumulate mercury as they prey on polluted ringed seals (Phoca hispida) and bearded seals (Erignathus barbatus). Studies have shown that polar bears from East Greenland are among the most mercury polluted species in the Arctic. It is unknown whether these levels are toxic to liver and kidney tissue. METHODS: We investigated the histopathological impact from anthropogenic long-range transported mercury on East Greenland polar bear liver (n = 59) and kidney (n = 57) tissues. RESULTS: Liver mercury levels ranged from 1.1–35.6 μg/g wet weight and renal levels ranged from 1–50 μg/g wet weight, of which 2 liver values and 9 kidney values were above known toxic threshold level of 30 μg/g wet weight in terrestrial mammals. Evaluated from age-correcting ANCOVA analyses, liver mercury levels were significantly higher in individuals with visible Ito cells (p < 0.02) and a similar trend was found for lipid granulomas (p = 0.07). Liver mercury levels were significantly lower in individuals with portal bile duct proliferation/fibrosis (p = 0.007) and a similar trend was found for proximal convoluted tubular hyalinisation in renal tissue (p = 0.07). CONCLUSION: Based on these relationships and the nature of the chronic inflammation we conclude that the lesions were likely a result of recurrent infections and ageing but that long-term exposure to mercury could not be excluded as a co-factor. The information is important as it is likely that tropospheric mercury depletion events will continue to increase the concentrations of this toxic heavy metal in the Sub Arctic and Arctic marine food webs
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