scholarly journals Long-Distance Movement of a Female Polar Bear from Canada to Russia

ARCTIC ◽  
2017 ◽  
Vol 70 (2) ◽  
pp. 121 ◽  
Author(s):  
Amy C. Johnson ◽  
Jodie D. Pongracz ◽  
Andrew E. Derocher

Polar bears (Ursus maritimus) display fidelity to large geographic regions, and their movements are influenced by sea ice distribution. Polar bear subpopulations are moderately distinct from one another, and long-distance movements between subpopulations are rare. We describe and analyze the movements of a female polar bear tracked by satellite telemetry from spring 2009 for 798 days. This female traveled an exceptionally long distance (totaling 11 686 km) from the sea ice off the Yukon Territory, Canada (Southern Beaufort Sea subpopulation) to Wrangel Island, Russia (Chukchi Sea subpopulation). In comparison to other polar bears in this study, this bear traveled farther, moved faster, and had a much larger home range in the first year. Furthermore, the calculation of the home range size by two different methods demonstrated that the commonly used minimum convex polygon method overestimated the home range compared to the less biased Brownian bridge movement model. This female’s long-distance movement was unusual and provides additional evidence for gene flow between subpopulations. Monitoring polar bear movements is useful to track such events, which is especially important at present because sea ice loss due to climate change can affect subpopulation boundaries and influence management.

Polar Biology ◽  
2011 ◽  
Vol 34 (7) ◽  
pp. 975-984 ◽  
Author(s):  
George M. Durner ◽  
John P. Whiteman ◽  
Henry J. Harlow ◽  
Steven C. Amstrup ◽  
Eric V. Regehr ◽  
...  

2016 ◽  
Vol 12 (12) ◽  
pp. 20160556 ◽  
Author(s):  
Eric V. Regehr ◽  
Kristin L. Laidre ◽  
H. Resit Akçakaya ◽  
Steven C. Amstrup ◽  
Todd C. Atwood ◽  
...  

Loss of Arctic sea ice owing to climate change is the primary threat to polar bears throughout their range. We evaluated the potential response of polar bears to sea-ice declines by (i) calculating generation length (GL) for the species, which determines the timeframe for conservation assessments; (ii) developing a standardized sea-ice metric representing important habitat; and (iii) using statistical models and computer simulation to project changes in the global population under three approaches relating polar bear abundance to sea ice. Mean GL was 11.5 years. Ice-covered days declined in all subpopulation areas during 1979–2014 (median −1.26 days year −1 ). The estimated probabilities that reductions in the mean global population size of polar bears will be greater than 30%, 50% and 80% over three generations (35–41 years) were 0.71 (range 0.20–0.95), 0.07 (range 0–0.35) and less than 0.01 (range 0–0.02), respectively. According to IUCN Red List reduction thresholds, which provide a common measure of extinction risk across taxa, these results are consistent with listing the species as vulnerable. Our findings support the potential for large declines in polar bear numbers owing to sea-ice loss, and highlight near-term uncertainty in statistical projections as well as the sensitivity of projections to different plausible assumptions.


2012 ◽  
Vol 90 (5) ◽  
pp. 663-676 ◽  
Author(s):  
A.M. Pagano ◽  
G.M. Durner ◽  
S.C. Amstrup ◽  
K.S. Simac ◽  
G.S. York

Polar bears ( Ursus maritimus Phipps, 1774) depend on sea ice for catching marine mammal prey. Recent sea-ice declines have been linked to reductions in body condition, survival, and population size. Reduced foraging opportunity is hypothesized to be the primary cause of sea-ice-linked declines, but the costs of travel through a deteriorated sea-ice environment also may be a factor. We used movement data from 52 adult female polar bears wearing Global Positioning System (GPS) collars, including some with dependent young, to document long-distance swimming (>50 km) by polar bears in the southern Beaufort and Chukchi seas. During 6 years (2004–2009), we identified 50 long-distance swims by 20 bears. Swim duration and distance ranged from 0.7 to 9.7 days (mean = 3.4 days) and 53.7 to 687.1 km (mean = 154.2 km), respectively. Frequency of swimming appeared to increase over the course of the study. We show that adult female polar bears and their cubs are capable of swimming long distances during periods when extensive areas of open water are present. However, long-distance swimming appears to have higher energetic demands than moving over sea ice. Our observations suggest long-distance swimming is a behavioral response to declining summer sea-ice conditions.


ARCTIC ◽  
2009 ◽  
Vol 61 (1) ◽  
pp. 14 ◽  
Author(s):  
Ian Stirling ◽  
Evan Richardson ◽  
Gregory W. Thiemann ◽  
Andrew E. Derocher

In April and May 2003 through 2006, unusually rough and rafted sea ice extended for several tens of kilometres offshore in the southeastern Beaufort Sea from about Atkinson Point to the Alaska border. Hunting success of polar bears (Ursus maritimus) seeking seals was low despite extensive searching for prey. It is unknown whether seals were less abundant in comparison to other years or less accessible because they maintained breathing holes below rafted ice rather than snowdrifts, or whether some other factor was involved. However, we found 13 sites where polar bears had clawed holes through rafted ice in attempts to capture ringed seals (Phoca hispida) in 2005 through 2006 and another site during an additional research project in 2007. Ice thickness at the 12 sites that we measured averaged 41 cm. These observations, along with cannibalized and starved polar bears found on the sea ice in the same general area in the springs of 2004 through 2006, suggest that during those years, polar bears in the southern Beaufort Sea were nutritionally stressed. Searches made farther north during the same period and using the same methods produced no similar observations near Banks Island or in Amundsen Gulf. A possible underlying ecological explanation is a decadal-scale downturn in seal populations. But a more likely explanation is major changes in the sea-ice and marine environment resulting from record amounts and duration of open water in the Beaufort and Chukchi seas, possibly influenced by climate warming. Because the underlying causes of observed changes in polar bear body condition and foraging behaviour are unknown, further study is warranted.


2017 ◽  
Vol 23 (9) ◽  
pp. 3460-3473 ◽  
Author(s):  
George M. Durner ◽  
David C. Douglas ◽  
Shannon E. Albeke ◽  
John P. Whiteman ◽  
Steven C. Amstrup ◽  
...  

2017 ◽  
Author(s):  
Susan J Crockford

The polar bear (Ursus maritimus) was the first species to be classified as threatened with extinction based on predictions of future conditions rather than current status. These predictions were made using expert-opinion forecasts of population declines linked to modeled habitat loss – first by the International Union for the Conservation of Nature (IUCN)’s Red List in 2006, and then by the United States Fish and Wildlife Service (USFWS) in 2008 under the Endangered Species Act (ESA), based on data collected to 2005 and 2006, respectively. Both assessments predicted significant population declines of polar bears would result by mid-century as a consequence of summer sea ice extent rapidly reaching 3-5 mkm2 on a regular basis: the IUCN predicted a >30% decline in total population, while the USFWS predicted the global population would decline by 67% (including total extirpation of ten subpopulations within two vulnerable ecoregions). Biologists involved in these conservation assessments had to make several critical assumptions about how polar bears might be affected by future habitat loss, since sea ice conditions predicted to occur by 2050 had not occurred prior to 2006. However, summer sea ice declines have been much faster than expected: low ice levels not expected until mid-century (about 3-5 mkm2) have occurred regularly since 2007. Realization of predicted sea ice levels allows the ‘rapid sea ice decline = population decline’ assumption for polar bears to be treated as a testable hypothesis. Data collected between 2007 and 2015 reveal that polar bear numbers have not declined as predicted and no subpopulation has been extirpated. Several subpopulations expected to be at high risk of decline remained stable and five showed increases in population size. Another at-risk subpopulation was not counted but showed marked improvement in reproductive parameters and body condition with less summer ice. As a consequence, the hypothesis that repeated summer sea ice levels of below 5 mkm2 will cause significant population declines in polar bears is rejected, a result that indicates the ESA and IUCN judgments to list polar bears as threatened based on future risks of habitat loss were scientifically unfounded and that similar predictions for Arctic seals and walrus may be likewise flawed. The lack of a demonstrable ‘rapid sea ice decline = population decline’ relationship for polar bears also potentially invalidates updated survival model outputs that predict catastrophic population declines should the Arctic become ice-free in summer.


2017 ◽  
Author(s):  
Susan J Crockford

The polar bear (Ursus maritimus) was the first species to be classified as threatened with extinction based on predictions of future conditions rather than current status. These predictions were made using expert-opinion forecasts of population declines linked to modeled habitat loss – first by the International Union for the Conservation of Nature (IUCN)’s Red List in 2006, and then by the United States Fish and Wildlife Service (USFWS) in 2008 under the Endangered Species Act (ESA), based on data collected to 2005 and 2006, respectively. Both assessments predicted significant population declines of polar bears would result by mid-century as a consequence of summer sea ice extent rapidly reaching 3-5 mkm2 on a regular basis: the IUCN predicted a >30% decline in total population, while the USFWS predicted the global population would decline by 67% (including total extirpation of ten subpopulations within two vulnerable ecoregions). Biologists involved in these conservation assessments had to make several critical assumptions about how polar bears might be affected by future habitat loss, since sea ice conditions predicted to occur by 2050 had not occurred prior to 2006. However, summer sea ice declines have been much faster than expected: low ice levels not expected until mid-century (about 3-5 mkm2) have occurred regularly since 2007. Realization of predicted sea ice levels allows the ‘rapid sea ice decline = population decline’ assumption for polar bears to be treated as a testable hypothesis. Data collected between 2007 and 2015 reveal that polar bear numbers have not declined as predicted and no subpopulation has been extirpated. Several subpopulations expected to be at high risk of decline remained stable and five showed increases in population size. Another at-risk subpopulation was not counted but showed marked improvement in reproductive parameters and body condition with less summer ice. As a consequence, the hypothesis that repeated summer sea ice levels of below 5 mkm2 will cause significant population declines in polar bears is rejected, a result that indicates the ESA and IUCN judgments to list polar bears as threatened based on future risks of habitat loss were scientifically unfounded and that similar predictions for Arctic seals and walrus may be likewise flawed. The lack of a demonstrable ‘rapid sea ice decline = population decline’ relationship for polar bears also potentially invalidates updated survival model outputs that predict catastrophic population declines should the Arctic become ice-free in summer.


2021 ◽  
Author(s):  
Erin M. Henderson ◽  
Andrew E. Derocher

The Cape Bathurst polynya and flaw lead (CBP) are major, predictable habitat features with ≤15% ice cover in an otherwise ice-covered Beaufort Sea, and thought to provide hunting opportunities for polar bears (Ursus maritimus Phipps, 1774). We assessed 78 adult (female; with and without cubs) and subadult (male and female) polar bears’ use of the CBP from October – June, 2007–2014. The CBP was up to 725 km wide in autumn, ice-covered in winter, and <306 km wide in spring. Seventy-nine percent (n = 62) of the bears used the CBP (≥1 location <2.4 km, or one 4 h step length, from the CBP). Use was higher for solitary adult females and subadult males, which travelled faster with low turning angles along wider sections than females with offspring and subadult females. Bears were closest to the CBP during the spring hyperphagia season. While a wider CBP did not prevent crossing, bears primarily crossed from the coast towards pack ice at locations 53% narrower than areas not crossed. Bears might avoid crossing when it would require a long-distance swim. The CBP affects polar bear ecology by providing hunting habitat and a corridor that could increase prey encounters but may affect movement.


2017 ◽  
Vol 472 (1) ◽  
pp. 17-20 ◽  
Author(s):  
V. V. Rozhnov ◽  
N. G. Platonov ◽  
S. V. Naidenko ◽  
I. N. Mordvintsev ◽  
E. A. Ivanov

2007 ◽  
Vol 85 (5) ◽  
pp. 596-608 ◽  
Author(s):  
T.W. Bentzen ◽  
E.H. Follmann ◽  
S.C. Amstrup ◽  
G.S. York ◽  
M.J. Wooller ◽  
...  

Ringed seals ( Phoca hispida Schreber, 1775 = Pusa hispida (Schreber, 1775)) and bearded seals ( Erignathus barbatus (Erxleben, 1777)) represent the majority of the polar bear ( Ursus maritimus Phipps, 1774) annual diet. However, remains of lower trophic level bowhead whales ( Balaena mysticetus L., 1758) are available in the southern Beaufort Sea and their dietary contribution to polar bears has been unknown. We used stable isotope (13C/12C, δ13C, 15N/14N, and δ15N) analysis to determine the diet composition of polar bears sampled along Alaska’s Beaufort Sea coast in March and April 2003 and 2004. The mean δ15N values of polar bear blood cells were 19.5‰ (SD = 0.7‰) in 2003 and 19.9‰ (SD = 0.7‰) in 2004. Mixing models indicated bowhead whales composed 11%–26% (95% CI) of the diets of sampled polar bears in 2003, and 0%–14% (95% CI) in 2004. This suggests significant variability in the proportion of lower trophic level prey in polar bear diets among individuals and between years. Polar bears depend on sea ice for hunting seals, and the temporal and spatial availabilities of sea ice are projected to decline. Consumption of low trophic level foods documented here suggests bears may increasingly scavenge such foods in the future.


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