Within their circumpolar range, polar bears (Ursus maritimus) are not subject to absolute barriers. However, physiographic features do cause discontinuities in their movements. These discontinuities in distribution can be used to delineate population units. Based on satellite telemetry of the movements of female polar bears carried out in 1989–1998, we used cluster analysis to identify 6 regions within the Canadian and western Greenland Arctic in which movements appear to be restricted enough to identify distinct populations. These regions generally correspond to management units that have been previously identified as Viscount Melville Sound, Lancaster Sound, Norwegian Bay, Kane Basin, Baffin Bay, and Davis Strait. A north–south substructure was identified for the Baffin Bay population, but it was weaker than the structure identified for the 6 primary units. The 6 units were consistent with genetic information, except for the Baffin Bay – Kane Basin separation, and with mark–recapture observations and the traditional knowledge of Inuit hunters. Only 2 of 65 bears that provided telemetry information for more than 1 year were classified in different populations in different years. However, annual rates of exchange, measured as the percentage of locations outside the population boundary, ranged from 0.4 to 8.9%. Analysis of mark–recapture movements indicated no difference in large-scale movements between the sexes or long-term movements with age. Although our validation criteria for demographic closure were satisfied, the observed rates of exchange between adjacent populations suggest that population dynamics in adjacent populations may not be completely independent.

The trophodynamics of per- and polyfluorinated compounds and bromine-based flame retardants were examined in components of a marine food web from the western Canadian Arctic. The animals studied and their relative trophic status in the food web, established using stable isotopes of nitrogen (delta15N), were beluga (Delphinapterus leucas) > ringed seal (Phoca hispida) > Arctic cod (Boreogadus saida) > Pacific herring (Clupea pallasi) approximately equal to Arctic cisco (Coregonus autumnalis) > pelagic amphipod (Themisto libellula) > Arctic copepod (Calanus hyperboreus). For the brominated diphenyl ethers, the lipid adjusted concentrations of the seven congeners analyzed (Sigma7BDEs: -47, -85, -99, -100, -153, -154, and -209) ranged from 205.4 +/- 52.7 ng/g in Arctic cod to 2.6 +/- 0.4 ng/g in ringed seals. Mean Sigma7BDEs concentrations in Arctic copepods, 16.4 ng/g (n = 2, composite sample), were greater than those in the top trophic level (TL) marine mammals and suggests that (i) Arctic copepods are an important dietary component that delivers BDEs to the food web and (ii) because these compounds are bioaccumulative, metabolism and depletion of BDE congeners in top TL mammals is an important biological process. There were differences in the concentration profiles of the isomers of hexabromocyclododecane (HBCD) in the food web. The most notable difference was observed for beluga, where the alpha-isomer was enriched (accounting for approximately 90% of the SigmaHBCD body burden), relative to its primary prey species, Arctic cod, where the alpha-isomer accounted for only 20% of the SigmaHBCD body burden (beta: 4% and gamma: 78%). For the C8-C11 perfluorinated carboxylic acids, the trophic magnification factors (TMFs) were all greater than unity and increased with increasing carbon chain length. PFOS and its neutral precursor, PFOSA, also had TMF values greater than one. There were also pronounced differences in the PFOSA to PFOS ratio in ringed seal (0.04) and in beluga (1.4) and suggests that, in part, there are differences in the efficacy of biotransforming PFOSA by whale and seal top predators that both preferentially feed on Arctic cod.

The mean home range size of female polar bears (Ursus maritimus; 125 100 km2 ± 11 800; n = 93) is substantially larger than the predicted value (514 km2) for a terrestrial carnivore of similar weight. To understand this difference, we correlated home range size and sea ice characteristics. Home range size was related to (i) the ratio of land vs. sea within a given home range (42% of explained variance), and (ii) seasonal variation in ice cover (24%). Thus, bears using land during the ice‐free season had larger home ranges and bears living in areas of great seasonal variation in ice cover also had larger home ranges. In another analysis we investigated how variation in a bear’s environment in space and time affects its choice of home range. We found that polar bears adjusted the size of their home range according to the amount of annual and seasonal variation within the centre of their home range. For example, polar bears experiencing unpredictable seasonal and annual ice tended to increase their home range size if increasing home range size resulted in reducing variation in seasonal and annual ice. Polar bears make trade‐offs between alternate space‐use strategies. Large home ranges occur when variable ice cover is associated with more seals but also a more unpredictable distribution of those seals.

As part of the Canadian contribution to the International Polar Year (IPY), several major international research programs have focused on offshore arctic marine ecosystems. The general goal of these projects was to improve our understanding of how the response of arctic marine ecosystems to climate warming will alter food web structure and ecosystem services provided to Northerners. At least four key findings from these projects relating to arctic heterotrophic food web, pelagic-benthic coupling and biodiversity have emerged: (1) Contrary to a long-standing paradigm of dormant ecosystems during the long arctic winter, major food web components showed relatively high level of winter activity, well before the spring release of ice algae and subsequent phytoplankton bloom. Such phenological plasticity among key secondary producers like zooplankton may thus narrow the risks of Climatic Change

Aging, often considered a result of random cellular damage, can be accurately estimated using DNA methylation profiles, the foundation of pan-tissue epigenetic clocks. Here, we demonstrate the development of universal pan-mammalian clocks, using 11,754 methylation arrays from our Mammalian Methylation Consortium, which encompass 59 tissue types across 185 mammalian species. These predictive models estimate mammalian tissue age with high accuracy (r > 0.96). Age deviations correlate with human mortality risk, mouse somatotropic axis mutations and caloric restriction. We identified specific cytosines with methylation levels that change with age across numerous species. These sites, highly enriched in polycomb repressive complex 2-binding locations, are near genes implicated in mammalian development, cancer, obesity and longevity. Our findings offer new evidence suggesting that aging is evolutionarily conserved and intertwined with developmental processes across all mammals.