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“…These findings emphasize the importance of understanding and incorporating the complexities of relationships between vital rates and environmental conditions in demographic assessments for management and conservation planning (Regehr et al. ), while highlighting the sensitivity of such assessments to variation and uncertainty in future environmental conditions.…”
Section: Discussionmentioning
confidence: 76%
“…, ), may not be suitable tools for addressing local management questions over shorter timeframes (e.g., setting of subsistence harvest levels) or for understanding how climate change and management actions interact to affect population viability (Regehr et al. ).…”
Changes in the abundance and distribution of wildlife populations are common consequences of historic and contemporary climate change. Some Arctic marine mammals, such as the polar bear (Ursus maritimus), may be particularly vulnerable to such changes due to the loss of Arctic sea ice. We evaluated the impacts of environmental variation on demographic rates for the Western Hudson Bay (WH), polar bear subpopulation from 1984 to 2011 using live-recapture and dead-recovery data in a Bayesian implementation of multistate capture-recapture models. We found that survival of female polar bears was related to the annual timing of sea ice break-up and formation. Using estimated vital rates (e.g., survival and reproduction) in matrix projection models, we calculated the growth rate of the WH subpopulation and projected population responses under different environmental scenarios while accounting for parametric uncertainty, temporal variation, and demographic stochasticity. Our analysis suggested a long-term decline in the number of bears from 1185 (95% Bayesian credible interval [BCI] = 993-1411) in 1987 to 806 (95% BCI = 653-984) in 2011. In the last 10 yr of the study, the number of bears appeared stable due to temporary stability in sea ice conditions (mean population growth rate for the period 2001-2010 = 1.02, 95% BCI = 0.98-1.06). Looking forward, we estimated long-term growth rates for the WH subpopulation of ~1.02 (95% BCI = 1.00-1.05) and 0.97 (95% BCI = 0.92-1.01) under hypothetical high and low sea ice conditions, respectively. Our findings support previous evidence for a demographic linkage between sea ice conditions and polar bear population dynamics. Furthermore, we present a robust framework for sensitivity analysis with respect to continued climate change (e.g., to inform scenario planning) and for evaluating the combined effects of climate change and management actions on the status of wildlife populations.
“…These findings emphasize the importance of understanding and incorporating the complexities of relationships between vital rates and environmental conditions in demographic assessments for management and conservation planning (Regehr et al. ), while highlighting the sensitivity of such assessments to variation and uncertainty in future environmental conditions.…”
Section: Discussionmentioning
confidence: 76%
“…, ), may not be suitable tools for addressing local management questions over shorter timeframes (e.g., setting of subsistence harvest levels) or for understanding how climate change and management actions interact to affect population viability (Regehr et al. ).…”
Changes in the abundance and distribution of wildlife populations are common consequences of historic and contemporary climate change. Some Arctic marine mammals, such as the polar bear (Ursus maritimus), may be particularly vulnerable to such changes due to the loss of Arctic sea ice. We evaluated the impacts of environmental variation on demographic rates for the Western Hudson Bay (WH), polar bear subpopulation from 1984 to 2011 using live-recapture and dead-recovery data in a Bayesian implementation of multistate capture-recapture models. We found that survival of female polar bears was related to the annual timing of sea ice break-up and formation. Using estimated vital rates (e.g., survival and reproduction) in matrix projection models, we calculated the growth rate of the WH subpopulation and projected population responses under different environmental scenarios while accounting for parametric uncertainty, temporal variation, and demographic stochasticity. Our analysis suggested a long-term decline in the number of bears from 1185 (95% Bayesian credible interval [BCI] = 993-1411) in 1987 to 806 (95% BCI = 653-984) in 2011. In the last 10 yr of the study, the number of bears appeared stable due to temporary stability in sea ice conditions (mean population growth rate for the period 2001-2010 = 1.02, 95% BCI = 0.98-1.06). Looking forward, we estimated long-term growth rates for the WH subpopulation of ~1.02 (95% BCI = 1.00-1.05) and 0.97 (95% BCI = 0.92-1.01) under hypothetical high and low sea ice conditions, respectively. Our findings support previous evidence for a demographic linkage between sea ice conditions and polar bear population dynamics. Furthermore, we present a robust framework for sensitivity analysis with respect to continued climate change (e.g., to inform scenario planning) and for evaluating the combined effects of climate change and management actions on the status of wildlife populations.
“…Future global population assessments could explore the use of hierarchical models [22], integrate data from multiple sources [23], model population processes (e.g. density-dependent interactions between harvest and habitat loss; [17]), consider cumulative effects on polar bear health [24] or consider nonlinear or spatial responses [25]. …”
Section: Resultsmentioning
confidence: 99%
“…Approach 3 estimated a separate ice – N relationship for each polar bear ecoregion using a dataset that was similar to approach 2 but included longer time series of N available for four subpopulations. All approaches assumed that changes in N were mediated primarily through changes in K or density-independent habitat effects, and that the ratio N / K was stable relative to other factors [17]. These assumptions were established on the basis that polar bears depend fundamentally on sea ice, that sea-ice changes represent the main source of habitat modification for the species [5], and that other potential stressors are either secondary (e.g.…”
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.
“…Subsequent to 1973, measures implemented by the Range States, such as increased research and monitoring, cooperative harvest management programs, and establishment of protected areas, were presumed to have either stabilized, or led to the recovery of, subpopulations that had experienced excessive unregulated harvest (Amstrup et al , Prestrud and Sterling ). Today, polar bears are legally harvested by Indigenous peoples in Alaska, Canada, and Greenland, and harvest levels in most subpopulations are well managed and occur at a rate that does not have a negative effect on population viability (Obbard et al , Regehr et al ).…”
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