Abstract
Given documented social dominance and intraspecific predation in bear populations, the ideal despotic distribution model and sex hypothesis of sexual segregation predict adult female grizzly bears (Ursus arctos) will avoid areas occupied by adult males to reduce risk of infanticide. Under ideal despotic distribution, juveniles should similarly avoid adult males to reduce predation risk. Den-site selection and use is an important component of grizzly bear ecology and may be influenced by multiple factors, including risk from conspecifics. To test the role of predation risk and the sex hypothesis of sexual segregation, we compared adult female (n = 142), adult male (n = 36), and juvenile (n = 35) den locations in Denali National Park and Preserve, Alaska, USA. We measured elevation, aspect, slope, and dominant land cover for each den site, and used maximum entropy modeling to determine which variables best predicted den sites. We identified the global model as the best-fitting model for adult female (area under curve (AUC) = 0.926) and elevation as the best predictive variable for adult male (AUC = 0.880) den sites. The model containing land cover and elevation best-predicted juvenile (AUC = 0.841) den sites. Adult females spatially segregated from adult males, with dens characterized by higher elevations ( = 1,412 m, SE = 52) and steeper slopes ( = 21.9°, SE = 1.1) than adult male (elevation: = 1,209 m, SE = 76; slope: = 15.6°, SE = 1.9) den sites. Juveniles used a broad range of landscape attributes but did not avoid adult male denning areas. Observed spatial segregation by adult females supports the sex hypothesis of sexual segregation and we suggest is a mechanism to reduce risk of infanticide. Den site selection of adult males is likely related to distribution of food resources during spring.
Introduction
Animal distribution theory has two pervasive models: the ideal free distribution and ideal despotic distribution models. The ideal free distribution model applies to non-territorial animals and states individuals are distributed proportionately to resources available [1]. Under this model, individuals assess the quality of available habitats and move unhindered among habitat units to select those considered best [1]. The ideal despotic distribution model applies to territorial animals, with dominant individuals displacing subordinates from higher quality habitats [2]. Subordinates' selection of habitat is therefore constrained by the distribution and behavior of dominant individuals [2]. This displacement in part forms an animal's realized niche [3]. Evidence for ideal despotic distribution has been demonstrated across a broad range of taxa [4]–[7].
Risk of predation and infanticide has long been hypothesized to influence behavior and resource selection in animals [8]–[12]. Though studies of evolutionary responses to risk have largely focused on predator/prey systems, evidence of these responses to conspecifics has also been found [10]–[23]. For example, dispersal in juvenile field voles (Microtus agrestis), cougars (Puma concolor), and Iberian lynx (Lynx pardinus) apparently serves in part to reduce risk from conspecifics [13], [17], [22]. Habitat selection by juvenile Atlantic cod (Gadus morhua) and seal salamanders (Desmognathus monticola) is also affected by risk from larger conspecifics [10], [16]. To reduce infanticide risk by unfamiliar males, many primate species have evolved permanent male-female associations [19]. Sexual segregation is another method by which mammal species with male-biased size dimorphism appear to reduce risk from conspecifics [11], [12], [14]. In some cases, female African lions (Panthera leo) and their young abandon prides and become temporarily nomadic when a new male has taken over, thus avoiding infanticide by the new dominant male [15]. Similarly, female alpine marmots (Marmota marmota) and their young may shift territories when new males encroach [18]. Resource partitioning between adult male and adult female cougars with young may also reduce risk of infanticide through sexual segregation [21], [23]. Though empirical evidence for decreased infanticide events in segregating individuals is lacking, segregated female alpine marmots did successfully wean young [18], [20]. Sexual segregation by mature females to protect young from immigrant adult males is known as the sex hypothesis of sexual segregation [14], [24].
Sexual size dimorphism is common in many species, including those with polygynous and promiscuous breeding strategies and has been demonstrated to result in sexual segregation [12], [23], [24]. In bear (Ursus spp.) populations, adult males are physically larger and dominant over other sex/age classes [12]. Increased body size in male bears is also positively associated with within-group dominance and increased breeding opportunities [25], [26], [27]. Consumption of abundant, highly digestible food increases grizzly bear (U. arctos) size and condition [28], [29]. Thus, individuals with access to high quality food sources benefit from increased body size, and therefore improved fitness [28].
Intraspecific predation has been observed in bear populations, in which adult males have killed juveniles (independent, non-breeding individuals) and adult females [30]–[33]. Although mechanisms driving intraspecific predation in bears are not completely understood, intraspecific aggression and population regulation may be involved [30]–[32], [34]. To reduce predation risk, juvenile grizzly bears may spatially and temporally segregate from dominant, non-kin adult males [35]–[37]. Sexual segregation has also been observed in grizzly bear populations, with mature females avoiding male-occupied habitats, potentially to reduce risk of infanticide [24]. Infanticide of unrelated young may provide a reproductive advantage for the infanticidal male, as females without young may be brought into estrous earlier and bred by the infanticidal male [38], [39]. In Alaska, spatial distribution of bears near salmon (Oncorhynchus spp.) streams appears driven by adult male bear presence, with adult females with young avoiding streams frequented by adult males [12]. Seasonal range size of adult females also appears influenced by risk of infanticide in Scandinavia, where oestrous females occupy a larger area during the mating season while females with cubs select small ranges to avoid males [11].
Den selection and use is an important component of bear ecology. Bear hibernation is generally attributed to limited food resources during winter [40], when bears reduce energetic costs by reducing metabolic rates [41]. Den sites may also provide thermal advantages and likely provide a secure location for parturition [42], [43]. Energetic demands of hibernation result in substantial body mass loss [29], [44]; therefore, it would be advantageous for all bears to locate dens near areas where food is likely to be abundant shortly after den emergence in spring. However, spatial segregation between sex/age groups of bears has been reported [45], [47]. Juveniles and adult females, particularly females with dependent young, may be more vulnerable to predation and infanticide by male bears during hibernation [30], [45]. Consequently, risk from conspecifics may influence den-site selection in grizzly bears. To reduce predation risk, juveniles may spatially or temporally segregate from adult males during the denning season. As infanticide is maladaptive to adult female grizzly bears, they may also modify timing and location of den sites to avoid males, as suggested for polar bears (U. maritimus; [46]).
To avoid detection by adult male grizzly bears, juveniles and adult females may den at higher elevations [45], [47], arrive at these sites earlier [47]–[49] and leave the denning area later [47]–[49] than adult male bears. Our objective was to test if spatial distribution of grizzly bear den sites supports the ideal despotic distribution model. We also tested whether the sex hypothesis of sexual segregation [14], under the umbrella of ideal despotic distribution theory, further explains den-site selection of adult female grizzly bears. We predicted that in order to reduce risk of infanticide and predation, adult females and juveniles spatially segregate from adult males by choosing den sites at higher elevations than adult males. We further predicted that adult females segregate to a greater extent than juveniles in order to protect their reproductive investment from potentially infanticidal males.
Methods
Ethics Statement
Ethics approval was not required at the time animal capture occurred. However, animal capture and handling procedures followed guidelines established by the American Veterinary Medical Association and American Society of Mammalogists.
Study Area
The study area encompassed about 7,068 km2 of Denali National Park and Preserve (63°3′24.63″N 150°49′19.44″W). Temperatures vary depending on elevation and season; reaching 32°C in summer and dropping to −47°C in winter [50]. Study area elevations range from 152–4,116 m. The region lies partially in the rain shadow of Denali and receives less precipitation than areas south of the mountain. Still, winter snow pack reaches depths of about 200 cm [50]. White spruce (Picea glauca), birch (Betula spp.), and aspen (Populus spp.) are common tree species from valley bottoms to about 700 m. Willow (Salix spp.) and alder (Alnus spp.) are common from about 500 m to treeline (500–1,300 m). Mountain avens (Dryas spp.) mats and lichens are abundant in tundra (≥1,000 m). Several forms of disturbance are common in the study area, including the Muldrow Glacier, ice action (erosion due to ice flows during spring break up) along waterways, and wildfires at lower elevations [50]. Population trends for the resident grizzly bears were summarized previously [51] and are generally stable, with an estimated lambda = 0.9963, SE = 0.0166. The estimated mean litter size for this population is 2.03 cubs/litter, and the estimated annual reproductive rate = 0.35, SE = 0.04. Cub and yearling survival rates are relatively low at about 0.34, SE = 0.04 and 0.60, SE = 0.07 respectively. Young generally stay with the mother for 2 years before dispersing. Subadult and adult survival rates are high at approximately 0.96, SE = 0.04 and 0.96, SE = 0.01 respectively. In addition to grizzly bears, the area supports populations of black bears (U. americanus), wolves (Canis lupus), caribou (Rangifer tarandus), and moose (Alces alces) [52]. Though there are few human settlements in the park, Denali National Park and Preserve receives 350,000–460,000 visitors annually (National Park Service 2010).
Data Collection
Between 1990–1998, grizzly bears were captured by Denali National Park and Preserve staff using aerial darting and fitted with very high frequency (VHF) radiocollars [53]. Bear ages were estimated by counting cementum annuli from an upper premolar (Matson's Laboratory, Milltown, Montana, USA) [54]. Bears were classified as adult female (≥5 years old), adult male (≥5 years old), or juvenile (≤4 years old). We used age four as the cut-off for juveniles based on later reproduction for northern grizzly bears [3], [55]. Den sites were located between September and May each winter using aerial telemetry, plotted on United States Geological Survey (USGS) 7.5 minute topographic maps, and converted to Universal Transverse Mercator grid coordinates.
Four landscape variables were used to classify the exact den locations (single pixel): land cover, elevation, slope, and aspect. Land cover was the dominant vegetation community or other surface cover type as classified by the Earth Satellite Corporation and the National Park Service (DENA Land Cover Mapping Project, ∼48 m2 pixel size, 2001). Several land cover types were combined based on vegetative similarities: open woodland spruce with open woodland/stunted spruce, broadleaf with mixed forest, alder shrub with willow shrub, low shrub/birch/willow with low shrub/sedge, dwarf shrub with dwarf shrub/rock, wet herbaceous with aquatic herbaceous, sparse vegetation with bare ground, and silty water with clear water for 12 cover types (Table 1). Elevation, slope, and aspect were obtained for the pixel containing each den site using a USGS digital elevation model (US GeoData – Alaska, ∼48 m2 pixel size, 2010). Elevation of each pixel was classified to the nearest meter and slope was classified as 0–90°. Aspect of each pixel was converted from degrees to a cardinal direction (north = 316–45°; east = 46–135°; south = 136–225°; west = 226–315°; or flat) [56]. All landscape data was extracted using ArcMap 3.9 (Environmental Systems Research Institute, Redlands, California, USA). From initial evaluations of habitat patch size, estimated maximum location error, and pixel resolution, accuracy of resource metrics extracted was appropriate for analyses [57], [58].
Table 1. Covertypes used to classify adult female, adult male, and juvenile grizzly bear den sites, Denali National Park and Preserve, Alaska, USA 1990–1998.
Covertype | Description |
Dense conifer forest | Dense canopy forest dominated by spruce |
Open woodland spruce | Open canopy forest dominated by spruce |
Broadleaf/mixed forest | Open or dense canopy forest with multiple species |
Alder/willow shrub | Shrub community dominated by alder and willow |
Closed low birch shrub | Dense shrub community dominated by birch |
Low shrub/birch/willow/sedge | Open or dense shrub community with multiple species |
Dwarf shrub | Open or dense shrub community with smaller plants |
Dry herbaceous | Open herbaceous community associated with drier sites |
Wet herbaceous | Open herbaceous community associated with wet sites |
Sparse vegetation | Characterized by mixture of bare soil, rock, and herbaceous plants |
Snow/ice | Characterized by year-round ice or snow |
Open water | Lakes and ponds |
Data Analysis
We tested for multicollinearity (r>0.7) of den-site variables to justify inclusion in candidate models. We used mixed model analysis of variance to compare den site landscape characteristics among adult female, adult male, and juvenile bears for relationships with elevation and slope. We controlled for repeated measures of bears (n≥1 den per individual) and treated year as a random effect, with bear ID nested within year. We used Tukey's range test for multiple comparisons. We compared den site aspects using chi-square analysis. We set α = 0.10 a priori for all analyses, as we expected our explanatory variables to vary greatly [58]. Land cover of den sites was summarized for each sex/age class. We also summarized variables between juvenile males and juvenile females to account for possible bias between these classes.
We used maximum entropy to model probable denning habitat (Maxent 3.3.3a; [56], [59]). Maximum entropy is a machine learning method for modeling species distributions from presence-only data, in which correlates at known locations are compared to the same correlates at 10,000 random points in the study area. Maximum entropy minimizes relative entropy between known location data and random point data [60]. Resulting models assign a 0 to 100 value (0 to 100% probability of occurrence) to all pixels, ranking them by relative suitability. Because maximum entropy compares presence locations to random locations, absence locations are not needed for analysis [61], [62].
We created separate models for adult female, adult male, and juvenile den sites using all variable combinations and each model was evaluated using receiver operating characteristic (ROC) plots. The ROC plots represent a model's ability to predict den locations and absences by plotting sensitivity against 1 – specificity [56]. We used the AUC statistic to select the most accurate model. Area under curve values range from 0.5 to 1.0, with 0.5 indicating no greater fit than expected by chance and 1.0 indicating perfect model fit [56]. We calculated standard errors for resulting AUC values by specifying that Maxent randomly set aside 30% of the den sites as test data. Maxent then used the remaining 70% of den sites as training data to fit a model, testing model fit using the test data. One problem with the AUC approach is that AUC values may be greatest for models with many variables even if some of those variables have negligible influence [56]. To account for this, we used a critical ratio test [63] to compare global models to the best 1–3 variable models for each sex/age class to see if improvement from additional variables was significant at α = 0.10. We then calculated Spearman rank correlation coefficients between competing models, and related the resulting coefficients to the table by Hanley and McNeil (1983) [64] to obtain adjusted correlation coefficients (r). These adjusted correlation coefficients were included in a critical ratio test [63]:
where A 1 is the AUC value for the highest-ranked model, A 2 is the AUC value for a lower-ranked model, and SE is the standard error for each respective model. We developed thresholds for probability of use by maximizing sensitivity and minimizing specificity and converted these results to a binary response of presence or absence [56]. Using the most parsimonious models, we mapped denning habitats of adult female, adult male, and juvenile grizzly bears.
Results
From 1990–1998, we located 142 adult female, 36 adult male, and 35 juvenile (20 male, 15 female) den sites. Den-site elevation and slope were similar between juvenile males (elevation: = 1,309 m, SE = 102; slope: = 20.2°, SE = 2.2) and juvenile females (elevation: = 1,332 m, SE = 109; slope: = 19.4°, SE = 3.6). Den-site elevation varied by gender/age class (F2,63 = 2.49, P = 0.091), with adult females denning at higher elevations than adult males (T58 = 2.22, P = 0.075). Juveniles denned at elevations similar to adult females (T66 = 1.02, P = 0.567) and adult males (T66 = 1.23, P = 0.443). Den-site slope also varied by sex/age class (F2,84 = 4.57, P = 0.013), with adult females denning on steeper slopes than adult males (T62 = 2.97, P = 0.011). Den-site slope of juveniles was similar to adult females (T111 = 1.45, P = 0.319) and adult males (T105 = 1.31, P = 0.391) (Table 2).
Table 2. Comparisons among grizzly bear den locations and habitat correlates for adult female (n = 142), adult male (n = 36), and juveniles (n = 35), Denali National Park and Preserve, Alaska, USA 1990–1998.
Adult Female | Adult Male | Juvenile | ||||
Variable | a | SE | a | SE | a | SE |
Elevation (m) | 1,412A | 52 | 1,209B | 76 | 1,329AB | 66 |
Slope (°) | 21.9A | 1.1 | 15.6B | 1.9 | 18.9AB | 1.9 |
Means not sharing a letter within rows differed significantly (P<0.10).
Bears showed non-random selection for aspect (χ2 8 = 15.96, P = 0.043) with adult females and juveniles using east and south-facing aspects and adult males using east and west-facing aspects more than expected (Table 3). Both juvenile males and juvenile females selected east and south-facing aspects. Dwarf shrub and sparse vegetation were the two primary land covers of den sites for all sex/age classes. However, percentage of dens in each land cover varied, with adult female dens relatively equally distributed (45% dwarf shrub, 36% sparse vegetation), adult male dens primarily in the dwarf shrub class (58% dwarf shrub, 17% sparse vegetation), and juvenile dens primarily in the sparse vegetation land cover (55% sparse vegetation, 27% dwarf shrub) (Table 3). Sparse vegetation was the most common land cover class for both juvenile males and juvenile females.
Table 3. Number of grizzly bear den sites by aspect and covertype for adult females (n = 142), adult males (n = 36), and juveniles (n = 35), Denali National Park and Preserve, Alaska, USA 1990–1998.
Variable | Class | Adult Female | Adult Male | Juvenile |
Aspect | North | 22 | 5 | 4 |
East | 43 | 15 | 10 | |
South | 43 | 5 | 12 | |
West | 34 | 11 | 7 | |
Flat | 0 | 0 | 2 | |
Covertype | Open woodland spruce | 1 | 3 | 1 |
Broadleaf/mixed forest | 0 | 0 | 1 | |
Alder/willow shrub | 4 | 1 | 0 | |
Closed low birch shrub | 0 | 0 | 1 | |
Low shrub/birch/willow/sedge | 6 | 4 | 2 | |
Dwarf shrub | 64 | 21 | 9 | |
Sparse vegetation | 51 | 6 | 18 | |
Snow/ice | 16 | 1 | 3 |
For maximum entropy modeling, we found no correlation between any variables for adult female or juvenile den sites (r≤0.70). Elevation and land cover was correlated for adult males (r = 0.72), thus, we did not run models containing elevation and land cover.
Best models for predicting den site use differed among adult females, adult males, and juveniles (Table 4). Based on AUC values and classification efficiency, the global model was most parsimonious for adult females (Fig. 1). This model was influenced most by elevation (contribution = 79.3%), followed by slope (12.7%), land cover (5.6%), and aspect (2.5%). Probability of den use increased with increasing elevation from 925 to 1,523 m, gradually decreased to 1,937 meters, and declined sharply thereafter (Fig. 2). Probability of den use also generally increased with increasing slope to 39°, declining thereafter. Den use was associated with east or south-facing aspects, and dwarf shrub/sparse vegetation land covers.
Table 4. Candidate maximum entropy models for adult female, adult male, and juvenile grizzly bear dens, Denali National Park and Preserve, Alaska, USA 1990–1998.
Age/Sex Class | Modela | AUC | SE | Z | P | Threshold | Class % |
Adult Female | ESVA | 0.926 | 0.002 | 19.900 | 83 | ||
ESV | 0.923 | 0.002 | 2.957 | 0.003 | 20.334 | 83 | |
EVA | 0.920 | 0.002 | 5.624 | <0.001 | 21.666 | 83 | |
ESA | 0.919 | 0.002 | 2.673 | 0.008 | 21.118 | 83 | |
EV | 0.916 | 0.002 | 9.373 | <0.001 | 19.426 | 81 | |
SVA | 0.910 | 0.002 | 11.153 | <0.001 | 29.190 | 83 | |
Adult Male | E | 0.880 | 0.013 | 48.141 | 80 | ||
EA | 0.854 | 0.015 | 2.707 | 0.007 | 41.686 | 80 | |
ES | 0.851 | 0.013 | 1.562 | 0.118 | 40.990 | 80 | |
ESA | 0.840 | 0.014 | 4.050 | <0.001 | 30.542 | 70 | |
SVA | 0.838 | 0.022 | 1.841 | 0.066 | 30.647 | 80 | |
VA | 0.831 | 0.027 | 1.849 | 0.065 | 33.814 | 80 | |
Juvenile | EV | 0.841 | 0.011 | 20.152 | 70 | ||
SVA | 0.824 | 0.012 | 1.893 | 0.058 | 18.824 | 80 | |
ESA | 0.823 | 0.013 | 1.067 | 0.286 | 31.640 | 70 | |
EVA | 0.823 | 0.013 | 1.071 | 0.284 | 19.478 | 80 | |
SV | 0.823 | 0.015 | 1.963 | 0.049 | 18.778 | 70 | |
ESVA | 0.819 | 0.012 | 3.088 | 0.002 | 14.922 | 70 |
Model abbreviations: E = elevation, S = slope, V = land cover, A = aspect.
We selected the model containing elevation for adult males. Probability of den use increased with increasing elevation from 300 to 1,334 m and declined for areas >1,334 m (Figs. 1, 3). We selected the model containing land cover (contribution = 90.6%) and elevation (9.4%) for juveniles (Figs. 1, 4). Probability of den use was greater in areas with sparse vegetation, closed low birch shrub, and dwarf shrub land covers. There was a comparatively wide range of elevations associated with juvenile den use, with probability of use increasing with increasing elevation from 300 to 1,500 m, followed by a gradual decline.
Discussion
Risk and Den-Site Selection
Predation risk did not appear to influence juvenile den-site selection. Juveniles selected a wide range of elevations that did not differ from those selected by adult males. Thus, juvenile den-site selection did not appear to follow the ideal despotic distribution model. While it is possible that adult males selectively kill juvenile males to eliminate potential competitors and increase breeding opportunities, small sample size for juvenile den locations (n = 35, 20 male, 15 female) precluded rigorous testing between juvenile females and juvenile males. Thus, we were unable to test whether this potential source of predation risk affected juvenile male den location. However, our results supported the ideal despotic distribution model and the sex hypothesis of sexual segregation for adult females, in that den-site selection differed between adult females and adult males, with maximum probability of den use for adult females at higher elevations than for adult males. The sex hypothesis of sexual segregation, coupled with adult females denning for longer periods of time than adult males [47]–[49], is the most likely explanation for observed adult female den use. As predation risk is similar for juveniles and adult females (the risk to the individual), we suggest that observed sexual segregation is a consequence of adult females avoiding adult males to reduce risk of infanticide (the added risk of losing their reproductive investment).
Although the mechanism for male den-site selection is unknown, we suggest the range of elevations selected by males was related to food availability at den emergence. Grizzly bears in Denali National Park and Preserve emerge from dens around May [50], coinciding with caribou parturition on their calving ground in our study area [65]. Den site elevation use of adult male grizzly bears overlapped extensively with the elevation range of the caribou calving ground, with highest number of newborn calves generally occurring from 900 to 1,500 m [65]. Mortality of caribou calves due to bear predation averaged 22% annually [50]. We suggest this concentrated and available food source was exploited by adult male grizzly bears to increase lean body mass following den emergence (e.g., Belant et al. 2006 [29]), leading to improved condition. Improved body condition (e.g., larger size) provides males with greater breeding opportunities in many species [26], [66]–[68].
In addition to denning at higher elevations, adult females entering dens earlier and emerging later may also be in response to infanticide risk [47]–[49]. Adult females, particularly those with young, should delay denning to maximize foraging opportunities before winter as percentage body fat in fall influences proportion of lean body mass lost during hibernation, and therefore animal condition [44]. However, we suggest that by moving to high elevation den locations early, adult females are further reducing the risk of infanticide, by moving through adult male denning areas before occupation by adult males. Likewise, it would be energetically advantageous for adult females to leave dens earlier to forage, because females with young lose more body mass than lone bears during hibernation [44]. However, this would necessitate adult females moving through high concentrations of adult males in denning areas. Further, the most readily available food in our study area in early spring was caribou calves or carcasses of animals that died in winter. These concentrated food sources are likely to attract multiple bears, including adult males, similar to concentrations of salmon [12], [69]. These food resources are therefore risky for adult females with young [12], [70]–[72]. Consequently, adult females may remain in high elevation dens to conserve energy, where longer snow cover increases thermal insulation and reduces energy loss, and wait for adult males to disperse from den areas and more dispersed food (e.g., herbaceous vegetation) to become available. We suggest that predation risk alone does not strongly influence den-site selection in grizzly bears. However, the added risk of infanticide appears to influence adult female den-site selection and contributes to spatial segregation between adult females and adult males.
Though not addressed in our hypotheses, our results suggest adult females may further spatially segregate by occupying steeper slopes than adult males [45]. This difference, however, may also be an artifact of the observed elevation gradient among sex/age classes as higher elevations often exhibit steeper slopes. Though elevation and slope differed between adult females and adult males, it is important to note there was considerable overlap. We suggest that while adult females attempted to sexually segregate, they were constrained by topographic (i.e., elevation) and structural (e.g., slope) features. These requirements likely limited how high and steep adult females could den, as very steep slopes are structurally unstable and the highest elevations in the study area have permafrost or little topsoil conducive to den excavation. Adult females in this study exhibited greatest selection for a narrow band of habitat near ridges (Fig. 5). Consequently, although segregation of adult females from adult males was observed, segregation may have been constrained by landscape features.
Den-Site Characteristics
Elevation was an important indicator of den sites for adult females and adult males, with high probability of use associated with mid-elevation portions of the study area. These elevations likely provided good insulative snow cover while remaining free of permafrost [30]. Although elevation was a predictor in the juvenile model, it only contributed 9.4% to model fit. The difference in contribution of elevation between juveniles and adult bears may be a consequence of inexperience. Resource use of juveniles often differs from adults and has been attributed to naïveté [73], [74], which may in part explain high observed variability in juvenile den elevation, resulting in low explanatory power.
Slope was moderately important for predicting adult female denning habitat, contributing 12.7% to model fit. Strongest selection was for slopes between 22–39°. These values are within the range reported in other studies, and likely were selected in part for structural stability and drainage properties [30], [75]–[78].
Land cover was the best predictor of juvenile denning habitat (contribution = 90.6%). Sparse vegetation and closed low birch shrub were the most probable cover types, followed by dwarf shrub. These cover types are indicative of higher elevation sites generally chosen for den sites. Land cover was also present in our adult female model but only contributed 5.6% to model fit. Sparse vegetation, dwarf shrub, and snow cover types were probable denning habitat. These cover types are consistent with den elevations, and we believe were an artifact of selection for elevation.
Conclusions
Risk from conspecifics influences resource selection in many species [10]–[23]. Adult male grizzly bears selected den sites in areas with abundant, high quality food available at den emergence (i.e., caribou calves [65]). We suggest that adult males selected these areas to improve individual fitness and increase breeding opportunities [26], [28]. That adult male and juvenile den-site selection was similar suggests predation risk was not a strong indicator of den-site selection by juveniles. However, risk of infanticide appeared to influence adult female den-site selection, with adult females selecting higher elevations and steeper slopes than adult males. We suggest sexual segregation is an important component of grizzly bear denning ecology, providing a mechanism by which adult females avoid infanticidal males. As adult male grizzly bears are the dominant sex/age group and adult female denning behavior appears suboptimal from an energetic perspective, observed sexual segregation supports the ideal despotic distribution model. While empirical evidence supporting sexual segregation to reduce infanticide is limited [18], [20], a growing body of literature suggests it occurs frequently across numerous taxa [15], [18], [21], [23], [24], [46].
Acknowledgments
We thank Denali National Park and Preserve staff for providing data. We also thank Dr. Sam Riffell and Dr. Roger Baldwin for assistance with statistical and GIS analysis.
Footnotes
Competing Interests: The authors have declared that no competing interests exist.
Funding: The National Park Service and the Mississippi State University Forest and Wildlife Research Center provided funding for this research. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
References
- 1.Fretwell SD, Lucas HL. On territorial behavior and other factors influencing habitat distribution in birds. I. Theoretical development. Acta Biotheoretica. 1970;19:16–36. [Google Scholar]
- 2.Fretwell SD. Populations in seasonal environments. Princeton: Princeton University Press; 1972. 224 [Google Scholar]
- 3.Belant JL, Griffith B, Zhang Y, Follmann EH, Adams LG. Population-level resource selection by sympatric brown and American black bears in Alaska. Polar Biology. 2010;33:31–40. [Google Scholar]
- 4.Murray CM, Mane SV, Pusey AE. Dominance rank influences female space use in wild chimpanzees, Pan troglodytes: towards an ideal despotic distribution. Animal Behaviour. 2007;74:1795–1804. [Google Scholar]
- 5.Oro D. Living in a ghetto within a local population: an empirical example of an ideal despotic distribution. Ecology. 2008;89:838–846. doi: 10.1890/06-1936.1. [DOI] [PubMed] [Google Scholar]
- 6.Purchase CF, Hutchings JA. A temporally stable spatial pattern in the spawner density of a freshwater fish: evidence for an ideal despotic distribution. Canadian Journal of Fisheries and Aquatic Sciences. 2008;65:382–388. [Google Scholar]
- 7.Smith JAM, Reitsma LR, Marra PP. Multiple space-use strategies and their divergent consequences in a nonbreeding migratory bird (Parkesia noveboracensis). Auk. 2011;128:53–60. [Google Scholar]
- 8.Festa-Bianchet M. Seasonal range selection in bighorn sheep: conflicts between forage quality, forage quantity, and predator avoidance. Oecologia. 1988;75:580–586. doi: 10.1007/BF00776423. [DOI] [PubMed] [Google Scholar]
- 9.Bergerud AT, Ferguson R, Butler HE. Spring migration and dispersion of woodland caribou at calving. Animal Behaviour. 1990;39:360–368. [Google Scholar]
- 10.Gotceitas V, Brown JA. Substrate selection by juvenile Atlantic cod (Gadus morhua): effects of predation risk. Oecologia. 1993;93:31–37. doi: 10.1007/BF00321187. [DOI] [PubMed] [Google Scholar]
- 11.Dahle B, Swenson JE. Seasonal range size in relation to reproductive strategies in brown bears Ursus arctos. Journal of Animal Ecology. 2003;72:660–667. doi: 10.1046/j.1365-2656.2003.00737.x. [DOI] [PubMed] [Google Scholar]
- 12.Rode KD, Farley SD, Robbins CT. Sexual dimorphism, reproductive strategy, and human activities determine resource use by brown bears. Ecology. 2006;87:2636–2646. doi: 10.1890/0012-9658(2006)87[2636:sdrsah]2.0.co;2. [DOI] [PubMed] [Google Scholar]
- 13.Myllymäki A. Intraspecific competition and home range dynamics in the field vole Microtus agrestis. Oikos. 1977;29:553–569. [Google Scholar]
- 14.Hrdy SB. Infanticide among animals: a review, classification, and examination of the implications for the reproductive strategies of females. Ethology and Sociobiology. 1979;1:13–40. [Google Scholar]
- 15.Packer C, Pusey AE. Adaptations of female lions to infanticide by incoming males. The American Naturalist. 1983;121:716–728. [Google Scholar]
- 16.Colley SA, Keen WH, Reed RW. Effects of adult presence on behavior and microhabitat use of juveniles of a desmognathine salamander. Copeia. 1989;1:1–7. [Google Scholar]
- 17.Beier P. Dispersal of juvenile cougars in fragmented habitat. Journal of Wildlife Management. 1995;59:228–237. [Google Scholar]
- 18.Coulon J, Graziani L, Allainé D, Bel MC, Puderoux S. Infanticide in the alpine marmot (Marmota marmota). Ethology Ecology & Evolution. 1995;7:191–194. [Google Scholar]
- 19.Van Schaik CP, Kappeler PM. Infanticide risk and the evolution of male–female association in primates. Proceedings of the Royal Society B: Biological Sciences. 1997;264:1687–1694. doi: 10.1098/rspb.1997.0234. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Ebensperger LA. Strategies and counterstrategies to infanticide in mammals. Biological Reviews. 1998;73:321–346. [Google Scholar]
- 21.Pierce BM, Bleich VC, Bowyer RT. Selection of mule deer by mountain lions and coyotes: effects of hunting style, body size, and reproductive status. Journal of Mammalogy. 2000;81:462–472. [Google Scholar]
- 22.Ferreras P, Delibes M, Palomares F, Fedriani JM, Calzada J, et al. Proximate and ultimate causes of dispersal in the Iberian lynx Lynx pardinus. Behavioral Ecology. 2004;15:31–40. [Google Scholar]
- 23.Keehner JR. Effects of reproductive status of mountain lions on prey selection of mule deer and white-tailed deer in northeastern Washington. 2009. MS Thesis. Washington State University.
- 24.Wielgus RB, Bunnell FL. Tests of hypotheses for sexual segregation in grizzly bears. Journal of Wildlife Management. 1995;59:552–560. [Google Scholar]
- 25.Stonorov D, Stokes A. Social behavior of the Alaska brown bear. Bears: Their Biology and Management. 1972;2:232–242. [Google Scholar]
- 26.Bellemain E, Zedrosser A, Manel S, Waits LP, Taberlet P, et al. The dilemma of female mate selection in the brown bear, a species with sexually selected infanticide. Proceedings of the Royal Society B. 2006;273:283–291. doi: 10.1098/rspb.2005.3331. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Kovach AI, Powell RA. Effects of body size on male mating tactics and paternity in black bears, Ursus americanus. Canadian Journal of Zoology. 2003;81:1257–1268. [Google Scholar]
- 28.Hilderbrand GV, Jenkins SG, Schwartz CC, Hanley TA, Robbins CT. Effect of seasonal differences in dietary meat intake on changes in body mass and composition in wild and captive brown bears. Canadian Journal of Zoology. 1999;77:1623–1630. [Google Scholar]
- 29.Belant JL, Kielland K, Follmann EH, Adams LG. Interspecific resource partitioning by sympatric ursids. Ecological Applications. 2006;16:2333–2343. doi: 10.1890/1051-0761(2006)016[2333:irpisu]2.0.co;2. [DOI] [PubMed] [Google Scholar]
- 30.Pearson AM. The northern interior grizzly bear Ursus arctos L. 1975. Canadian Wildlife Service Report Series 34, Ottawa, Canada.
- 31.Taylor MK, Larsen T, Schweinsburg RE. Observations of intraspecific aggression and cannibalism in polar bears (Ursus maritimus). Arctic. 1985;38:303–309. [Google Scholar]
- 32.Case RL, Buckland L. Reproductive characteristics of grizzly bears in the Kugluktuk area, Northwest Territories, Canada. Ursus. 1998;10:41–47. [Google Scholar]
- 33.Swenson JE, Dahle B, Sandegren F. Intraspecific predation in Scandinavian brown bears older than cubs-of-the-year. Ursus. 2001;12:81–91. [Google Scholar]
- 34.Bunnell FL, Tait DEN. Dynamics of large mammal populations. New York: Wiley; 1981. 477 [Google Scholar]
- 35.Mattson DJ, Knight RR, Blanchard BM. The effects of developments and primary roads on grizzly bear habitat use in Yellowstone National Park, Wyoming. International Conference on Bear Research and Management. 1987;7:259–273. [Google Scholar]
- 36.Gunther KA. Visitor impact on grizzly bear activity in Pelican Valley, Yellowstone National Park. International Conference on Bear Research and Management. 1990;8:73–78. [Google Scholar]
- 37.Mattson DJ. Human impacts on bear habitat use. International Conference on Bear Research and Management. 1990;8:33–56. [Google Scholar]
- 38.Swenson JE, Sandegren F, Söderberg A, Bjärvall A, Franzén R, et al. Infanticide caused by hunting of male bears. Nature. 1997;386:450–451. [Google Scholar]
- 39.Bellemain E, Swenson JE, Taberlet P. Mating strategies in relation to sexually selected infanticide in a nonsocial carnivore: the brown bear. Ethology. 2006;111:1–14. [Google Scholar]
- 40.Nelson RA. Protein and fat metabolism in hibernating bears. Federal Proceedings. 1980;39:2955–2958. [PubMed] [Google Scholar]
- 41.Folk GE., Jr . Textbook of environmental physiology. Philadelphia: Lea and Febiger; 1974. 468 [Google Scholar]
- 42.Nelson RA. Winter sleep in the black bear: a physiologic and metabolic marvel. Mayo Clinic Proceedings. 1973;48:733–737. [PubMed] [Google Scholar]
- 43.Harding LE. Den-site characteristics of arctic coastal grizzly bears (Ursus arctos L.) on Richards Island, Northwest Territories, Canada. Canadian Journal of Zoology. 1976;54:1357–1363. [Google Scholar]
- 44.Hilderbrand GV, Schwartz CC, Robbins CT, Hanley TA. Effect of hibernation and reproductive status on body mass and condition of coastal brown bears. Journal of Wildlife Management. 2000;64:178–183. [Google Scholar]
- 45.Schoen JW, Beier LW, Lentfer JW, Johnson LJ. Denning ecology of brown bears on Admiralty and Chichagof Islands. International Conference on Bear Research and Management. 1987;7:293–304. [Google Scholar]
- 46.Derocher AE, Stirling I. Distribution of polar bears (Ursus maritimus) during the ice-free period in western Hudson Bay. Canadian Journal of Zoology. 1990;68:1395–1403. [Google Scholar]
- 47.Haroldson MA, Ternent MA, Gunther KA, Schwartz CC. Grizzly bear denning chronology and movements in the Greater Yellowstone Ecosystem. Ursus. 2002;13:29–37. [Google Scholar]
- 48.McLoughlin PD, Cluff HD, Messier F. Denning ecology of barren-ground grizzly bears in the central arctic. Journal of Mammalogy. 2002;83:188–198. doi: 10.1007/s00442-002-0941-5. [DOI] [PubMed] [Google Scholar]
- 49.Manchi S, Swenson JE. Denning behavior of Scandinavian brown bears Ursus arctos. Wildlife Biology. 2005;11:123–132. [Google Scholar]
- 50.Mech LD, Adams LG, Meier TJ, Burch JW, Dale BW. The wolves of Denali. Minneapolis: University of Minnesota Press; 1998. 240 [Google Scholar]
- 51.Owen PA, Mace RD. Grizzly bear population ecology in Denali National Park and Preserve. Alaska Park Science: Crossing Boundaries in a Changing Environment. 2006;6:67–69. [Google Scholar]
- 52.Sheldon C. The wilderness of Denali: explorations of a hunter-naturalist in northern Alaska. New York: Charles Scribner's Sons; 1930. 432 [Google Scholar]
- 53.Taylor WP, Reynolds HV, Ballard WB. Immobilization of grizzly bears with tiletamine hydrochloride and zolazepam hydrochloride. Journal of Wildlife Management. 1989;53:978–981. [Google Scholar]
- 54.Craighead JJ, Craighead FC, McCutchen HE. Age determination of grizzly bears from fourth premolar tooth sections. Journal of Wildlife Management. 1970;34:353–363. [Google Scholar]
- 55.Leland PG, Miller LH. Seasonal movements of an Alaska Peninsula brown bear population. Bears: Their Biology and Management. 1980;4:307–312. [Google Scholar]
- 56.Baldwin RA, Bender LC. Den-site characteristics of black bears in Rocky Mountain National Park, Colorado. Journal of Wildlife Management. 2008;72:1717–1724. [Google Scholar]
- 57.Montgomery RA, Roloff GJ, Ver Hoef JM, Millspaugh JJ. Can we accurately characterize wildlife resource use when telemetry data are imprecise? Journal of Wildlife Management. 2010;74:1917–1925. [Google Scholar]
- 58.Montgomery RA, Roloff GJ, Ver Hoef JM. Implications of ignoring telemetry error on inference in wildlife resource use models. Journal of Wildlife Management. 2011;75:702–708. [Google Scholar]
- 59.Schauber EM, Edge WD. Statistical power to detect main and interactive effects on small mammal population attributes. Canadian Journal of Zoology. 1999;77:68–73. [Google Scholar]
- 60.Phillips SJ, Anderson RP, Schapire RE. Maximum entropy modeling of species geographic distributions. Ecological Modelling. 2006;190:231–259. [Google Scholar]
- 61.Elith J, Phillips SJ, Hastie T, Dudik M, Chee YE, et al. A statistical explanation of MaxEnt for ecologists. Diversity and Distributions. 2011;17:43–57. [Google Scholar]
- 62.Johnson KG, Pelton MR. Selection and availability of dens for black bears in Tennessee. Journal of Wildlife Management. 1981;45:111–119. [Google Scholar]
- 63.Oli MK, Jacobson HA, Leopold BD. Denning ecology of black bears in the White River National Wildlife Refuge, Arkansas. Journal of Wildlife Management. 1997;61:700–706. [Google Scholar]
- 64.Pearce J, Ferrier S. Evaluating the predictive performance of habitat models developed using logistic regression. Ecological Modelling. 2000;133:225–245. [Google Scholar]
- 65.Hanley JA, McNeil BJ. A method of comparing the areas under receiver operating characteristic curves derived from the same cases. Radiology. 1983;148:839–843. doi: 10.1148/radiology.148.3.6878708. [DOI] [PubMed] [Google Scholar]
- 66.Adams LG, Dale BW, Mech LD. Wolf predation on caribou calves in Denali National Park, Alaska. In: Carbyn LN, Fritts SH, Seip DR, editors. Ecology and conservation of wolves in a changing world. Edmonton: Canadian Circumpolar Institute, University of Alberta; 1995. pp. 245–260. [Google Scholar]
- 67.McCann TS. Aggression and sexual activity of male southern elephant seals, Mirounga leonine. Journal of Zoology. 1981;195:295–310. [Google Scholar]
- 68.Ruby DE. Male breeding success and differential access to females in Anolis carolinensis. Herpetologica. 1984;40:272–280. [Google Scholar]
- 69.Reid ML, Roitberg BD. Effects of body size on investment in individual broods by male pine engravers (Coleoptera: Scolytidae). Canadian Journal of Zoology. 1995;73:1396–1401. [Google Scholar]
- 70.Ben-David M, Titus K, Beier L. Consumption of salmon by Alaskan brown bears: a trade-off between nutritional requirements and the risk of infanticide. Oecologia. 2004;138:465–474. doi: 10.1007/s00442-003-1442-x. [DOI] [PubMed] [Google Scholar]
- 71.Luque MH, Stokes AW. Fishing behavior of Alaska brown bear. International Conference on Bear Research and Management. 1976;3:71–78. [Google Scholar]
- 72.McClellan B. Density-dependent population regulation of brown bears. In: Taylor M, editor. Density-dependent population regulation in black, brown, and polar bears. International Conference on Bear Research and Management Monograph Series 3; 1994. pp. 15–24. [Google Scholar]
- 73.Chi DK. The effects of salmon availability, social dynamics, and people on black bear (Ursus americanus) fishing behavior on Alaskan salmon stream. 1999. Dissertation. Utah State University.
- 74.Sjöberg M, Ball JP. Grey seal, Halichoerus grypus, habitat selection around haulout sites in the Baltic Sea: bathymetry or central-place foraging? Canadian Journal of Zoology. 2000;78:1661–1667. [Google Scholar]
- 75.Krebs J, Lofroth E, Copeland J, Banci V, Cooley D, et al. Synthesis of survival rates and causes of mortality in North American wolverines. Journal of Wildlife Management. 2004;68:493–502. [Google Scholar]
- 76.Reynolds HV, Curatolo JA, Quimby R. Denning ecology of grizzly bears in northeastern Alaska. International Conference on Bear Research and Management. 1976;3:403–409. [Google Scholar]
- 77.Vroom GW, Herrero S, Ogilvie RT. The ecology of winter den sites of grizzly bears in Banff National Park, Alberta. International Conference on Bear Research and Management. 1980;4:321–330. [Google Scholar]
- 78.Servheen CW, Klaver R. Grizzly bear dens and denning activity in the Mission and Rattlesnake Mountains, Montana. International Conference on Bear Research and Management. 1983;5:201–207. [Google Scholar]