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Newediuk, L.

Publications and source records attributed to Newediuk, L..

9 recordsLinked to original sources

Mutation and Recombination Rates in Free-Ranging Polar Bears

Mutation rate () and recombination rate (r) are fundamental population-genetic parameters, yet demographic and conservation inference in polar bears (Ursus maritimus) has relied on values borrowed from humans and other mammals. Known values vary by an order of magnitude across mammals, and inaccuracies in these estimates propagate into downstream analyses, such as inferences of demographic history. To address this, we used high-coverage whole-genome resequencing of eight parent-offspring trios from the Western Hudson Bay subpopulation of polar bears. We identified 329 de novo mutations and estimated a pedigree-based germline mutation rate of 1.22 x 10?? per site per generation, which is within the mammalian range and close to values previously assumed for this species. Trio-based phasing yielded 522 crossovers across 16 meioses (32.6 per meiosis), and a pedigree-inferred recombination rate of 1.50 cM/Mb. From 44 unrelated individuals sampled from the same subpopulation, we inferred a demography-aware recombination map with a length-weighted genome-wide recombination rate of 3.03 cM/Mb (median 1.28 cM/Mb). We also identified 8,515 recombination hotspot regions covering 2.10% of the genome, accounting for 43.8% of total map length, a 20.9-fold concentration. Crossovers overlapped LD-defined hotspots 5.06-fold more often than expected by chance (p < 0.001). Nucleotide diversity was low and positively rank-correlated with recombination rate, consistent with linked selection. Genomic features explained only ~3% of recombination rate variation, with GC content and SINE abundance the only significant predictors. These species-specific parameters provide an empirical foundation for future demographic reconstruction and population projection in this vulnerable, ice-obligate species.

genomics↗

When blood is not thicker than water: Social information landscapes offset the food-fear trade-off in habitat selection decisions

1. Group foraging reduces the risks associated with foraging: larger groups dilute individual predation risk, allow group members to share the costs of vigilance, and provide a social structure for exchanging information about predators. The benefits of shared social information over simple safety in numbers should depend on the relationships among group members. Consequently, group composition should affect the selection of risky and safe habitats in social species. 2. We asked whether relationships among elk (Cervus canadensis) group members moving together influence their selection of risky habitats more than grouping alone. We tested three hypotheses. The familiarity hypothesis predicts that elk with close social ties are most likely to select risky habitats together. The inclusive fitness hypothesis predicts that the closest genetic relatives are most likely to select risky habitats together. The dilution hypothesis predicts that familiarity and genetic relationships do not influence habitat selection, with all group foraging benefits derived from proximity to others. 3. We used integrated Step Selection Analysis to test whether the identity of the closest group members influenced habitat selection. We tested whether the relationship of the nearest elk--either genetic or social--incentivized selection of risky habitat more than proximity to the nearest elk. 4. Group foraging clearly reduced risk, with elk more likely to select risky habitat when near others. Elk were also more likely to select risky habitats when near closer relatives, albeit with considerable variation among individuals. However, familiarity had a large and consistent effect: elk were far more likely to select risky habitats when near socially familiar group members. 5. Our results suggest that information shared within foraging groups, especially between socially familiar individuals, may lower the risks associated with habitat selection. Similarly, the benefits of reliable social information for reducing risk likely incentivizes the formation of stronger social ties within foraging groups. This positive feedback between social familiarity and habitat selection could thereby increase access to profitable habitats that are otherwise too risky, cementing what we term the social information landscape as a key driver of movement and habitat selection.

ecology↗

Sociality shapes context-dependent stress responses to anthropogenic disturbance in African elephants

Social relationships can buffer individuals against environmental challenges, reducing the physiological costs of disturbance. Assessing how social and environmental conditions jointly shape physiological stress is critical for predicting individual responses to disturbance, particularly in managed populations. We evaluated whether social and environmental stressors act additively or whether social context modifies physiological responses to environmental challenges. We combined behavioural data and faecal glucocorticoid metabolite samples from a small, intensively monitored population of African elephants (Loxodonta africana) in a fenced reserve. Using a Bayesian framework, we tested how social factors interacted with variation in the biophysical environment, including natural environmental and anthropogenic disturbances, to predict glucocorticoid concentrations. Natural environmental variables, including weather, water availability, and season, did not predict glucocorticoid concentrations. In contrast, helicopter use, a common management intervention, was associated with higher glucocorticoid concentrations. Social effects were context dependent. Following disturbance, low-ranking individuals showed higher glucocorticoid concentrations than high-ranking individuals, whereas this pattern reversed under low-disturbance conditions. Individuals with more social connections had lower glucocorticoid concentrations, but this effect was evident only under non-disturbance conditions. Measures of betweenness centrality did not predict glucocorticoid levels. These results demonstrate that social factors mediate physiological responses to anthropogenic disturbance and that management actions can impose uneven physiological costs across individuals. Quantifying interactions between social factors and the biophysical environment may improve conservation and management strategies for social species. Integrating physiological responses to interactions between social factors and the biophysical environment can guide conservation strategies and improve management interventions in social species.

animal behavior and cognition↗

Revisiting Size Selective Morality in Young Fish: Do Small Teleosts Really Pay a Cost?

Small juvenile and larval teleosts are typically more susceptible to starvation and predation, so the largest individuals tend to survive. However, most support for this bigger is better hypothesis is experimental and does not account for the variation in food availability, competition, and other conditions that alter how starvation and predation affect small fish. To assess how natural populations experience size-selective mortality, we reviewed the past 30 years of literature on the subject while compiling 76 effect sizes of longitudinal survival data, which evaluates selection against size classes, to test for evidence that bigger is better. Our meta-analysis shows that the effect of body size on survival is consistently weak across species, populations, times, and locations. We discuss several reasons why larger young teleosts may not have a distinct survival advantage. We argue that they: 1) may be more profitable or noticeable to predators, 2) are unable to outgrow all their predators, and 3) require more resources, increasing their predator exposure out of necessity to forage. We recommend that mortality not be treated as constant across young teleost size classes, as different ecological conditions may favour smaller, larger, or neither size class. We suggest that the relationship between metabolic scope and mortality, geographic gradients in the importance of predation and starvation, and the interactive effects of alternative sources of mortality with predation and starvation in warming oceans are underexplored and could change how we think about the relationship between young teleost size and survival. Investigating these drivers will be important as temperatures rapidly rise, altering growth in wild fish.

ecology↗

Not so scary after all? Decoding the landscape of fear through hormonal responses to risky times and places

Prey must balance the energetic benefits of foraging with avoiding predation risk. This risk-reward trade-off, a cornerstone of behavioural ecology, hinges not only on realized predation risk but also on how prey perceive that risk. We often assume energetically rewarding habitats must be inherently risky because prey often increase their vigilance in these habitats or avoid them altogether. However, our assumption that these antipredator behaviours reflect perceived risk frequently goes untested. We used non-behavioural data to test our assumptions about which habitats prey perceive as risky by pairing observations of habitat use of elk (Cervus canadensis) with their physiological responses measured from faecal hormones: glucocorticoids (GC), which reflect stress from perceived risk and hunger, and triiodothyronine (T3), which increases with energy intake. Elk had lower GC and T3 in the forest, a putatively safer and poorer foraging habitat than cropland, where they produced more T3, indicating foraging. Surprisingly, GC levels were consistent in cropland, even during the daytime when human activity--and putative risk--peaked. This lack of risk responsiveness highlights that physiological responses are a nuanced integration of perceived risk and reward rather than a guaranteed outcome of habitat use. Our study challenges the assumption that high-reward habitats are inherently risky, and that safer habitats limit energy intake, revealing that the assumptions we make about habitats from a behavioural lens may not always be the reality for prey.

ecology↗

Climate change, age acceleration, and the erosion of fitness in polar bears

Climate change is increasingly disrupting evolved life history strategies and reducing population viability in wild species. Using estimates of epigenetic age acceleration, a cellular biomarker of lifetime stress and the expression of age-related phenotypes, we found that polar bears aged approximately one year faster for each degree of warming since the 1960s. Age acceleration was also associated with reproducing early in life, linking this cellular process to well-established life history theory. However, we found evidence for the erosion of fitness as epigenetic aging accelerated and temperatures increased. Finally, using a large pedigree, we found adaptive potential in our study population was approximately zero. Global temperatures will soon reach the levels of warming currently experienced by Arctic species, which could impose widespread physiological costs and limit adaptive capacities worldwide.

ecology↗

Migration distance and mating system are not associated with genetic diversity and differentiation among bats (Chiroptera)

Genetic variation is critical for evolutionary responses to environmental change. Links between genetic variation and behavioural or life history traits may reveal how varied strategies influence evolutionary trends in speciation and adaptation. Traits associated with movement typically correlate with population genetic structure and could help predict populations vulnerability to geographic processes such as habitat fragmentation and disease spread. With their wide diversity in behaviours and ecologies, bats provide a useful testing ground for hypotheses about population structure related to species-specific movement patterns. We used a global sample of microsatellite data (n=233 sites from 17 bat species) associated with published studies to examine potential links between genetic variation and migration and mating strategies. The genetic measures we tested were population-specific differentiation, gene diversity, and allelic richness. Using Bayesian models that accounted for phylogenetic distances among species, we identified no correlations between migration or mating strategy and genetic variation. Our results do not support long-standing hypotheses about dispersal-mediated genetic structure, and contrast with prior studies on bat genetic diversity and differentiation. We discuss the need for continued research into the complex association of ecological, biogeographical, and behavioural factors that facilitate gene flow among populations, especially in species with diverse movement patterns.

zoology↗

Unifying adaptive stress and adaptive habitat selection hypotheses through movement ecology

The cort-adaptation and cort-fitness hypotheses both propose glucocorticoids produced by parents mediate trade-offs between their own survival and that of their offspring. The contribution of glucocorticoids to offspring provisioning can quantify these trade-offs because provisioning poses a risk to parents. However, attributing provisioning behaviour to glucocorticoids is difficult because glucocorticoids often drive foraging behaviours to store energy for later provisioning. We compared the effects of glucocorticoids on habitat selection before and after calving to test for the trade-offs female elk make when provisioning offspring. Despite finding that female elk with elevated glucocorticoids selected more strongly for high-risk, high-forage cropland, we found no difference in glucocorticoid production nor a significant change in the effect of glucocorticoids on cropland selection at calving time when lactating elk required the more energy. However, we found a gradual increase in the effect of glucocorticoids on cropland selection by female elk as their calves grew, suggesting the growing energy requirements of calves encouraged more risky habitat selection behaviours by their parents over time. We suggest trade-offs in investment between parents and offspring across life history stages can be tested by integrating glucocorticoids into habitat selection models. Ultimately, this integration will help elucidate the adaptive function of glucocorticoids.

ecology↗

Solving the Sample Size Problem for Resource Selection Analysis

O_LISample size sufficiency is a critical consideration for conducting Resource-Selection Analyses (RSAs) from GPS-based animal telemetry. Cited thresholds for sufficiency include a number of captured animals M [&ge;] 30 and as many relocations per animal N as possible. These thresholds render many RSA-based studies misleading if large sample sizes were truly insufficient, or unpublishable if small sample sizes were sufficient but failed to meet reviewer expectations. C_LIO_LIWe provide the first comprehensive solution for RSA sample size by deriving closed-form mathematical expressions for the number of animals M and the number of relocations per animal N required for model outputs to a given degree of precision. The sample sizes needed depend on just 2 biologically meaningful quantities: habitat selection strength and a novel measure of landscape complexity, which we define rigorously. The mathematical expressions are calculable for any environmental dataset at any spatial scale and are applicable to any study involving resource selection (including sessile organisms). We validate our analytical solutions using globally relevant empirical data including 5,678,623 GPS locations from 511 animals from 10 species (omnivores, carnivores, and herbivores living in boreal, temperate, and tropical forests, montane woodlands, swamps, and arctic tundra). C_LIO_LIOur analytic expressions show that the required M and N must decline with increasing selection strength and increasing landscape complexity, and this decline is insensitive to the definition of availability used in the analysis. Our results contradict conventional wisdom by demonstrating that the most biologically relevant effects on the utilization distribution (i.e. those landscape conditions with the greatest absolute magnitude of resource selection) can often be estimated with far fewer data than is commonly assumed. C_LIO_LIWe identify several critical steps in implementing these equations, including (i) a priori selection of expected model coefficients, and (ii) sampling intensity for background (absence/pseudo-absence) data within a given definition of availability. We show that random sampling of background data violates the underlying mathematics of RSA, leading to incorrect values for necessary M and N and potentially incorrect RSA model outputs. We argue that these equations should be a mandatory component for all future RSA studies. C_LI

ecology↗