Estimating population size and density of a low-density population of black bears in Rocky Mountain National Park, Colorado

Rocky Mountain National Park (RMNP) is home to a low-density black bear (Ursus americanus) population that exists at >2,400?m with a very limited growing season. A previous study (1984–1991) found bear densities among the lowest reported (1.37–1.52 bears/100?km²). Because of concerns of viability of this small population, we assessed population size and density of black bears from 2003 to 2006 to determine the current status of RMNP’s bear population. We used three approaches to estimate population size and density: (1) minimum number known, (2) occupancy modeling, and (3) catch per unit effort (CPUE). We used information from capture and remote-triggered cameras, as well as visitor information, to derive a minimum known population estimate of 20–24 individuals and a median density estimate of 1.35 bears/100?km². Bear occupancy was estimated at 0.46 (SE?=?0.11), with occupancy positively influenced by lodgepole pine stands, non-vegetated areas, and patch density but negatively influenced by mixed conifer stands. We combined the occupancy estimate with mean home-range size and overlap for bears in RMNP to derive a density estimate of 1.44 bears/100?km². We also related CPUE to density estimates for eight low-density black bear populations to estimate density in RMNP; this estimate (1.03 bears/100?km²) was comparable to the occupancy estimate and suggests that this approach may be useful for future population monitoring. The use of corroborative techniques for assessing population size of a low-density black bear population was effective and should be considered for similar low-density wildlife populations.     

Unraveling the mystery of the glacier bear: Genetic population structure of black bears (Ursus americanus) within the range of a rare pelage type

Glacier bears are a rare grey color morph of American black bear (Ursus americanus) found only in northern Southeast Alaska and a small portion of western Canada. We examine contemporary genetic population structure of black bears within the geographic extent of glacier bears and explore how this structure relates to pelage color and landscape features of a recently glaciated and highly fragmented landscape. We used existing radiocollar data to quantify black bear home‐range size within the geographic range of glacier bears. The mean home‐range size of female black bears in the study area was 13 km² (n = 11), whereas the home range of a single male was 86.9 km². We genotyped 284 bears using 21 microsatellites extracted from noninvasively collected hair as well as tissue samples from harvested bears. We found ten populations of black bears in the study area, including several new populations not previously identified, divided largely by geographic features such as glaciers and marine fjords. Glacier bears were assigned to four populations found on the north and east side of Lynn Canal and the north and west side of Glacier Bay with a curious absence in the nonglaciated peninsula between. Lack of genetic relatedness and geographic continuity between black bear populations containing glacier bears suggest a possible unsampled population or an association with ice fields. Further investigation is needed to determine the genetic basis and the adaptive and evolutionary significance of the glacier bear color morph to help focus black bear conservation management to maximize and preserve genetic diversity.     

Home ranges of brown bears on the Kamchatka peninsula and Sakhalin Island

Territorial activity was studied using satellite tracking of four brown bears (Ursus arctos) in Kamchatka in 2005–2006 and three brown bears on Sakhalin in 2011–2012. The size of annual home ranges was 6.09–27.58 km² for females and 153.12 km² for males. The size of the nuclear zone of the annual home ranges did not exceed 1.68 km². Seasonal home ranges were largest in August-September and smallest in May. The home ranges of two females in Kamchatka were significantly overlapped, the lesser degree of overlap was noted for two females on Sakhalin. The nature of the use of the study area by bears, essentially depends on the seasonal distribution of food, in particular salmon.     

Black bear spatial responses to the Wallow Wildfire in Arizona

The Wallow Fire, the largest wildfire in Arizona history, encompassed 2,170 km² and provided a rare opportunity to examine habitat selection and home ranges of American black bears (Ursus americanus) before and after a wildfire. We had fitted global positioning system (GPS) collars on 47 bears from 2005 to April 2011, and 10 of these were still collared when the fire started in May 2011. We captured and collared an additional 7 black bears within the fire perimeter post-fire (Jul–Sep 2011 and Jun 2012). To evaluate how black bears were affected by the fire, we fit a step selection function using a conditional mixed effects Poisson regression model to estimate the relative strength of black bear habitat selection in response to burn severity. Additionally, we estimated home range sizes using an autocorrelated kernel density estimator by means of a continuous-time movement model. We then used a generalized linear model with a negative binomial error distribution and mixed effects to estimate the effect of the burn severity on black bear home range size, while controlling for sex and drought. In spring and summer in years prior to the fire, bears selected areas that later burned in the fire. After the fire, bears used all burn severities, but their selection for high-severity burns decreased significantly in summer 2011 and fall 2012. Home range sizes were 3.06 times larger pre-fire than post-fire. Our study demonstrates that black bears continued to use all burn severities after a major wildfire, and that post-fire conditions did not result in expanded black bear home ranges.     

Space Use and Habitat Selection by Female Louisiana Black Bears in the Tensas River Basin of Louisiana

Abstract: Studies of space use and habitat selection of endangered species are useful for identifying factors that influence fitness of individuals and viability of populations. However, there is a lack of published information regarding these behaviors for the federally threatened Louisiana black bear (Ursus americanus luteolus). We documented space use and habitat selection for 28 female black bears in 2 subpopulations of the Tensas River Basin population in northeast Louisiana, USA. The Tensas subpopulation inhabits a relatively large (>300-km²) contiguous area of bottomland hardwood forest, whereas the Deltic subpopulation exists mainly in 2 small (<7-km²) forested patches surrounded by an agricultural matrix. Females on Deltic maintained smaller seasonal and annual home ranges than females on Tensas (all P < 0.04), except for females with cubs during spring. On Tensas, females with cubs maintained smaller home ranges than females without cubs during spring (P = 0.01), but we did not detect this difference on Deltic or in other seasons. Females on Tensas and Deltic exhibited differences in habitat selection when establishing home ranges and within home ranges (P < 0.001). Deltic females selected mature bottomland hardwood forests and avoided agricultural habitats at both spatial scales. Tensas females selected a mixture of swamps, mature and regenerating forests, and exhibited variation in selection across scale, season, and reproductive status. We suggest that differences in space use and habitat selection between Tensas and Deltic are at least partially due to habitat differences at the landscape (i.e., amount of forested habitat) and patch (i.e., food availability) scales. Our results contribute to the understanding of factors that influence space use and habitat selection by black bears and provide specific information on habitat types selected by Louisiana black bears to agencies involved in habitat protection and restoration for this threatened subspecies.     

Extensive Predator Space Use Can Limit the Efficacy of a Control Program

ABSTRACT Reduced to small isolated groups by anthropogenic habitat losses or habitat modifications, populations of many endangered species are sensitive to additive sources of mortality, such as predation. Predator control is often one of the first measures considered when predators threaten survival of a population. Unfortunately, predator ecology is often overlooked because relevant data are difficult to obtain. For example, the endangered Gaspésie caribou (Rangifer tarandus caribou) has benefited from 2 periods of predator control that targeted black bears (Ursus americanus) and coyotes (Canis latrans) in an attempt to reduce predation on caribou calves. Despite a high trapping effort, the number of predators removed has remained stable over time. To assess impact of predator movements on efficacy of a control program, we studied space use of 24 black bears and 16 coyotes over 3 years in and around the Gaspésie Conservation Park, Quebec, Canada, using Global Positioning System radiocollars. Annual home ranges of black bears averaged 260 km² and 10 individuals frequented area used by caribou. Annual home ranges of resident coyotes averaged 121 km², whereas dispersing coyotes covered >2,600 km². Coyotes were generally located at lower altitudes than caribou. However, because coyotes undertook long-distance excursions, they overlapped areas used by caribou. Simulations based on observed patterns showed that 314 bears and 102 coyotes potentially shared part of their home range with areas used by female caribou during the calving period. Despite low densities of both predator species, extensive movement and use of nonexclusive territories seem to allow predators to rapidly occupy removal areas, demonstrating the need for recurrent predator removals. Our results underscore the necessity of considering complementary and alternative solutions to predator control to assure long-term protection of endangered species.     

Space use and site fidelity of wintering whooping cranes on the Texas Gulf Coast

The Aransas-Wood Buffalo population (the only non-reintroduced, migratory population) of endangered whooping cranes (Grus americana) overwinters along the Texas Gulf Coast, USA. Understanding whooping crane space use on the wintering grounds reveals essential aspects of this species' ecology, which subsequently assists with conservation. Using global positioning system telemetry data from marked whooping cranes during 2009–2017, we fit continuous-time stochastic process models to describe movement and home range using autocorrelated kernel density estimation (AKDE) and explored variation in home range size in relation to age, sex, reproductive status, and drought conditions. We used the Bhattacharyya coefficient of overlap and distance between home range centroids to quantify site fidelity. We examined the effects of time between winter home ranges and the sex of the crane on site fidelity using Bayesian mixed-effects beta regression. Winter whooping crane 95% AKDE home range size averaged 30.1 ± 45.2 (SD) km² (median = 14.3, range = 1.1–308.6). Home ranges of sub-adult females were approximately 2 times larger than those of sub-adult males or families. As drought worsened, home ranges typically expanded. Between consecutive years, the home ranges of an adult crane exhibited 68 ± 31% overlap (site fidelity), but fidelity to winter sites declined in subsequent winters. The overlap of adult home ranges with the nearest unrelated family averaged 33 ± 28%. As a whooping crane aged, overlap with its winter home range as a juvenile declined, regardless of sex. By 4 years of age, a whooping crane had approximately 14 ± 28% overlap with its juvenile winter home range. Limited evidence suggested male whooping cranes return to within 2 km of their juvenile home range by their fifth winter. Previous data obtained from aerial surveys led ecologists to assume that whooping crane families normally used small areas (~2 km²) and expressed persistent site fidelity. Our analyses showed <8% of families had home ranges ≤2 km², with the average area 15 times greater, and waning site fidelity over time. Our work represents an analysis of whooping crane home ranges for this population, identifying past misconceptions of winter space use and resulting in better estimates of space requirements for future conservation efforts.     

Black Bear Movement and Food Conditioning in an Exurban Landscape

Conflicts between humans and wildlife have become increasingly important challenges for resource managers along the urban-wildland interface. Food conditioning (i.e., reliance by an animal on anthropogenic foods) of American black bears (Ursus americanus) is related to conflict behavior (i.e., being bold or aggressive toward humans, consuming human food or garbage, causing property damage) and often occurs in communities adjacent to Great Smoky Mountains National Park (GRSM or Park), USA. The goal of our study was to evaluate black bear space use in GRSM and in exurban areas on surrounding private lands and to identify factors associated with food conditioning and conflict behavior. We radio-collared 53 bears (29 males, 24 females) from 2015 to 2017 to compare space use characteristics and used carbon isotopic signatures (δ¹³C) from bear hair to assess food conditioning. We then performed an integrated step selection function (iSSF) analysis to characterize and compare movement and resource use as related to food conditioning. Based on the stable isotope analyses, 24 bears were classified as food conditioned (FC; 16 males and 8 females) and 37 were not food conditioned (NFC; 14 males and 23 females). Annual 95% kernel density estimate (KDE) home ranges and 50% KDE core area estimates of female and male bears did not differ by level of food conditioning (i.e., mean δ¹³C), but 95% and 50% home ranges of FC females were smaller than NFC females when data from 2015, a year of food scarcity and abnormally large home ranges, were excluded. The mean proportion of exurban development (e.g., roads, buildings, openings) within 95% KDE and 50% KDE home ranges of females increased with mean δ¹³C (i.e., greater food conditioning). The iSSF models indicated that FC bears were more likely to use forest openings associated with higher levels of development than NFC bears. We used those models to demonstrate how landscape modifications can reduce bear use of exurban areas, particularly for NFC bears. Our stable isotope, movement, and resource use data indicate that conflict behaviors displayed by many bears within GRSM were learned in areas outside Park boundaries. © 2020 The Wildlife Society.     

Estimates of Abundance and Harvest Rates of Female Black Bears Across a Large Spatial Extent

American black bears (Ursus americanus) are an iconic wildlife species in the southern Appalachian highlands of the eastern United States and have increased in number and range since the early 1980s. Given an increasing number of human-bear conflicts in the region, many management agencies have liberalized harvest regulations to reduce bear populations to socially acceptable levels. Wildlife managers need reliable population data for assessing the effects of management actions for this high-profile species. Our goal was to use DNA extracted from hair collected at barbed-wire enclosures (i.e., hair traps) to identify individual bears and then use spatially explicit capture-recapture methods to estimate female black bear density, abundance, and harvest rate. We established 888 hair traps across 66,678 km² of the southern Appalachian highlands in Georgia, North Carolina, South Carolina, and Tennessee, USA, in 2017 and 2018, arranged in 174 clusters of 2–9 traps/cluster. We collected 9,113 hair samples from those sites over 6 weeks of sampling, of which 1,954 were successfully genotyped to 462 individual female bears. Our spatially explicit estimator included a percent forest covariate to explain inhomogeneous bear density across the region. Densities ranged up to 0.410 female bears/km² and regional abundance was 5,950 (95% CI = 4,988–7,098) female bears. Based on hunter kill data from 2016 to 2018, mean annual harvest rates for females were 12.7% in Georgia, 17.6% in North Carolina, 17.6% in South Carolina, and 22.8% in Tennessee. Our estimated harvest rates for most states approached or exceeded theoretical maximum sustainable levels, and population trend data (i.e., bait-station indices) indicated decreasing growth rates since about 2009. These data suggest that the increased harvest goals and poor hard mast production over a series of prior years reduced bear population abundance in many states. We were able to obtain reasonable population abundance and density estimates because of spatially explicit capture-recapture methods, cluster sampling, and a large spatial extent. Continued monitoring of bear populations (e.g., annual bait-station surveys and periodic population estimation using spatially explicit methods) by state jurisdictions would help to ensure that population trajectories are consistent with management goals. © 2021 The Wildlife Society.     

Space Use,Survival, Movements,and Reproduction of Reintroduced Louisiana Black Bears

ABSTRACT Studies of reintroduced animals are beneficial to evaluate the success of reintroduction programs and to understand factors influencing fitness of reintroduced individuals. The geographic distribution of the federally threatened Louisiana black bear (Ursus americanus luteolus) has been reduced to 3 isolated populations due to habitat loss and excessive harvest. We reintroduced 23 adult female Louisiana black bears and their cubs to east-central Louisiana, USA, and documented postrelease space use, survival, movements, and reproduction. Individual females used larger home ranges after reintroduction than they had in the source population (P = 0.037). Spring ranges of reintroduced females were smaller than summer, autumn, and annual ranges (all P < 0.09), which did not differ from each other (all P > 0.60). Survival of reintroduced females did not differ between their first (S = 0.933) and second (S = 1.00) year after release or from annual survival of females in the source population (S = 0.964–1.00). Mean straight-line distance traveled by females from their release sites to the center of established home ranges or last recorded locations was 22.7 km. Six females reproduced after reintroduction and produced 15 cubs. Mean postrelease litter size of parturient reintroduced females (2.5) was similar to reported mean litter size of females in the source population (2.4). Our results suggest that the Louisiana reintroduction program is proceeding favorably; however, future studies should continue to monitor survival and reproduction of reintroduced females in Louisiana. Additional demographic parameters (i.e., cub survival) should be estimated to allow for population viability analysis to determine if the new population is self-sustaining.     

Spatial variation in density of American black bears in northern Yellowstone National Park

The quality and availability of resources are known to influence spatial patterns of animal density. In Yellowstone National Park, relationships between the availability of resources and the distribution of grizzly bears (Ursus arctos) have been explored but have yet to be examined in American black bears (Ursus americanus). We conducted non-invasive genetic sampling during 2017–2018 (mid-May to mid-July) and applied spatially explicit capture-recapture models to estimate density of black bears and examine associations with landscape features. In both years, density estimates were higher in forested vegetation communities, which provide food resources and thermal and security cover preferred by black bears, compared with non-forested areas. In 2017, density also varied by sex, with female densities being higher than males. Based on our estimates, the northern range of Yellowstone National Park supports one of the highest densities of black bears (20 black bears/100 km²) in the northern Rocky Mountains (6–12 black bears/100 km² in other regions). Given these high densities, black bears could influence other wildlife populations more than previously thought, such as through displacement of sympatric predators from kills. Our study provides the first spatially explicit estimates of density for black bears within an ecosystem that contains the majority of North America's large mammal species. Our density estimates provide a baseline that can be used for future research and management decisions of black bears, including efforts to reduce human–bear conflicts.     

Conflict Bear Translocation: Investigating Population Genetics and Fate of Bear Translocation in Dachigam National Park,Jammu and Kashmir,India

The Asiatic black bear population in Dachigam landscape, Jammu and Kashmir is well recognized as one of the highest density bear populations in India. Increasing incidences of bear-human interactions and the resultant retaliatory killings by locals have become a serious threat to the survivorship of black bears in the Dachigam landscape. The Department of Wildlife Protection in Jammu and Kashmir has been translocating bears involved in conflicts, henceforth ‘conflict bears’ from different sites in Dachigam landscape to Dachigam National Park as a flagship activity to mitigate conflicts. We undertook this study to investigate the population genetics and the fate of bear translocation in Dachigam National Park. We identified 109 unique genotypes in an area of ca. 650 km² and observed bear population under panmixia that showed sound genetic variability. Molecular tracking of translocated bears revealed that mostly bears (7 out of 11 bears) returned to their capture sites, possibly due to homing instincts or habituation to the high quality food available in agricultural croplands and orchards, while only four bears remained in Dachigam National Park after translocation. Results indicated that translocation success was most likely to be season dependent as bears translocated during spring and late autumn returned to their capture sites, perhaps due to the scarcity of food inside Dachigam National Park while bears translocated in summer remained in Dachigam National Park due to availability of surplus food resources. Thus, the current management practices of translocating conflict bears, without taking into account spatio-temporal variability of food resources in Dachigam landscape seemed to be ineffective in mitigating conflicts on a long-term basis. However, the study highlighted the importance of molecular tracking of bears to understand their movement patterns and socio-biology in tough terrains like Dachigam landscape.     

Integrating sign surveys and telemetry data for estimating brown bear (Ursus arctos) density in the Romanian Carpathians

Accurate population size estimates are important information for sustainable wildlife management. The Romanian Carpathians harbor the largest brown bear (Ursus arctos) population in Europe, yet current management relies on estimates of density that lack statistical oversight and ignore uncertainty deriving from track surveys. In this study, we investigate an alternative approach to estimate brown bear density using sign surveys along transects within a novel integration of occupancy models and home range methods. We performed repeated surveys along 2‐km segments of forest roads during three distinct seasons: spring 2011, fall‐winter 2011, and spring 2012, within three game management units and a Natura 2000 site. We estimated bears abundances along transects using the number of unique tracks observed per survey occasion via N‐mixture hierarchical models, which account for imperfect detection. To obtain brown bear densities, we combined these abundances with the effective sampling area of the transects, that is, estimated as a function of the median (± bootstrapped SE) of the core home range (5.58 ± 1.08 km²) based on telemetry data from 17 bears tracked for 1‐month periods overlapping our surveys windows. Our analyses yielded average brown bear densities (and 95% confidence intervals) for the three seasons of: 11.5 (7.8–15.3), 11.3 (7.4–15.2), and 12.4 (8.6–16.3) individuals/100 km². Across game management units, mean densities ranged between 7.5 and 14.8 individuals/100 km². Our method incorporates multiple sources of uncertainty (e.g., effective sampling area, imperfect detection) to estimate brown bear density, but the inference fundamentally relies on unmarked individuals only. While useful as a temporary approach to monitor brown bears, we urge implementing DNA capture–recapture methods regionally to inform brown bear management and recommend increasing resources for GPS collars to improve estimates of effective sampling area.     

Dispersal of Yearling Pronghorns in Western South Dakota

Abstract: We captured and radiocollared 57 pronghorn (Antilocapra americana) fawns in western South Dakota, USA, during May 2002–2003 and radiotracked them through 15 months of age, by which time all surviving individuals had established a permanent home range. We classified 56% (n = 19) of fawns as dispersers and 44% (n = 15) as residents. Eighty-four percent (n = 16) of dispersers departed natal home ranges in late October and occupied winter home ranges for 102–209 days before dispersing to permanent home ranges during April 2003 and 2004. Dispersal distances from natal ranges to permanent home ranges varied from 6.2–267.0 km. Winter home-range sizes for all individual pronghorns varied from 39.4–509.6 km. Permanent home-range size for all individuals varied from 15.5–166.1 km². Mean 95% permanent home-range size differed (P = 0.06) between residents (x̄ = 97.3 ± 15.1 km²) and dispersers (x̄ = 48.6 ± 16.0 km²), but was similar (P = 0.97) among sexes. Mean dispersal distance from natal to permanent home ranges was similar (P = 0.35) for males (x̄ = 54.2 ± 21.0 km) and females (x̄ = 26.3 ± 19.9 km). We suggest that habitat quality (i.e., patchiness) and pronghorn density, in part, stimulated dispersal. We hypothesize that as habitat patch size decreases, home range sizes and distance traveled during predispersal and dispersal movements by pronghorns will increase.     

Differential Range Use between Age Classes of Southern African Bearded Vultures Gypaetus barbatus

Bearded Vulture Gypaetus barbatus movements were investigated in southern Africa to determine whether an individual''s age, sex or breeding status influenced its ranging behaviour and to provide the information required to guide conservation activities. Data from satellite transmitters fitted to 18 individuals of four age classes were used to determine range size and use. Because of the nature of the movements of marked individuals, these data could be used to determine the overall foraging range of the entire population, which was estimated to be 51 767 km². Although juvenile, immature and sub-adult birds used different parts of the overall range, their combined foraging range was 65% (33 636 km²) of the overall range. Average adult home ranges (286 km²) were only around 1% the size of the average foraging ranges of non-adults (10 540 –25 985 km²), with those of breeding adults being even smaller (95 km²). Home ranges of breeding adults did not vary in size between seasons but adults utilized their home range more intensively whilst breeding, moving greater distances during the incubation and chick hatching period. Range size and use increased as non-adults aged. Immatures and sub-adults had larger range sizes during winter, but range use of non-adults did not vary seasonally. Range size and use did not differ between the sexes in any of the age classes. Information on home range size and use enables specific areas within the species'' range to be targeted for management planning, education and conservation action.     

Extreme home range sizes among Eurasian lynx at the northern edge of their biogeographic range

Eurasian lynx (Lynx lynx) have a wide distribution across Eurasia. The northern edge of this distribution is in Norway, where they reach up to 72 degrees north. We conducted a study of lynx space use in this region from 2007 to 2013 using GPS telemetry. The home range sizes averaged 2,606 (± 438 SE) km² for males (n = 9 ranges) and 1,456 (± 179 SE) km² for females (n = 24 ranges). These are the largest home ranges reported for any large felid, and indeed are only matched by polar bears, arctic living wolves, and grizzly bears among all the Carnivora. The habitat occupied was almost entirely treeless alpine tundra, with home ranges only containing from 20% to 25% of forest. These data have clear implications for the spatial planning of lynx management in the far north as the current management zones are located in unsuitable habitats and are not large enough to encompass individual lynx movements.     

Factors associated with black bear density and implications for management

Wildlife density estimates are important to accurately formulate population management objectives and understand the relationship between habitat characteristics and a species’ abundance. Despite advances in density and abundance estimation methods, management of common game species continues to be challenged by a lack of reliable population estimates. In Washington, USA, statewide American black bear (Ursus americanus) abundance estimates are predicated on density estimates derived from research in the 1970s and are hypothesized to be a function of precipitation and vegetation, with higher densities in western Washington. To evaluate current black bear density and landscape relationships in Washington, we conducted a 4-year capture-recapture study in 2 areas of the North Cascade Mountains using 2 detection methods, non-invasive DNA collection and physical capture and deployment of global positioning system (GPS) collars. We integrated GPS telemetry from collared bears with spatial capture-recapture (SCR) data and created a SCR-resource selection model to estimate density as a function of spatial covariates and test the hypothesis that density is higher in areas with greater vegetative food resources. We captured and collared 118 bears 132 times and collected 7,863 hair samples at hair traps where we identified 537 bears from 1,237 detections via DNA. The most-supported model in the western North Cascades depicted a negative relationship between black bear density and an index of human development. We estimated bear density at 20.1 bears/100 km², but density varied from 13.5/100 km² to 27.8 bears/100 km² depending on degree of human development. The model best supported by the data in the eastern North Cascades estimated an average density of 19.2 bears/100 km², which was positively correlated with primary productivity, with resulting density estimates ranging from 7.1/100 km² to 33.6 bears/100 km². The hypothesis that greater precipitation and associated vegetative production in western Washington supports greater bear density compared to eastern Washington was not supported by our data. In western Washington, empirically derived average density estimates (including cubs) were nearly 50% lower than managers expected prior to our research. In eastern Washington average black bear density was predominantly as expected, but localized areas of high primary productivity supported greater than anticipated bear densities. Our findings underscore the importance that black bear density is not likely uniform and management risk may be increased if an average density is applied at too large a scale. Disparities between expected and empirically derived bear density illustrate the need for more rigorous monitoring to understand processes that affect population numbers throughout the jurisdiction, and suggest that management plans may need to be reevaluated to determine if current harvest strategies are achieving population objectives. © 2019 The Wildlife Society.     

Resource Selection by Recolonizing American Black Bears

American black bears (Ursus americanus) were extirpated from Oklahoma, USA, in the early twentieth century but have since recolonized eastern portions of the state after immigrating from Arkansas, where they were successfully translocated. Within the last 2 decades, a population of black bears was detected in the Oklahoma Ozark region, prompting studies to determine population size, growth rate, and genetic makeup. To understand how black bears were recolonizing the human-dominated landscape, we investigated resource selection at 2 scales. Between 2011 and 2016, we collected global positioning system collar spatial data for 10 males and 13 females. We calculated average kernel density home ranges on a seasonal scale for all collared bears. We used generalized linear mixed models to calculate resource selection functions at the study area, defined by locations of all radio-collared black bears (second order) and the scale of individual black bear home ranges (third order). Resource selection did not differ significantly by sex. Black bears across seasons and scales selected riparian forest and moist oak (Quercus spp.) forest land cover types and mostly selected against indicators of human activity (e.g., pasture-prairie, anthropogenic land cover types, roads, and areas of high human population density). Black bears also selected areas with rugged terrain at high elevations, although not consistently across seasons and scales. Black bear recolonization appeared to be negatively affected by areas and features characterized as human-altered. Further expansion of the range of black bears may be limited by anthropogenic disturbance in the region. © 2021 The Wildlife Society.     

Space use and territoriality of wolverines (<Emphasis Type="Italic">Gulo gulo</Emphasis>) in northern Scandinavia

Space use and territoriality influence population structure and dynamics and is therefore an important aspect in understanding the ecology of animals. We investigated spatial and temporal space use of wolverines (Gulo gulo) in northern Scandinavia. We estimated home ranges of 24 radio-marked individuals (17 females and seven males). Male home ranges (mean 669 km²; SE = 211) were significantly larger than female home ranges (mean 170 km²; Wilcoxon–Mann–Whitney; P = 0.001) and encompassed or included parts of up to five different females. Home range sizes of reproducing (170 km²; SE = 51) and barren (171 km²; SE = 63) adult females did not differ. Wolverines in Scandinavia exhibit intrasexual territoriality, with male home ranges totally exclusive and female home ranges either exclusive or with little home range overlap. Overlap between wolverine territories is most likely explained by intrasexual tolerance and kinship.     

Dietary adjustability of grizzly bears and American black bears in Yellowstone National Park

Grizzly bears (Ursus arctos) and American black bears (U. americanus) are sympatric in much of Yellowstone National Park. Three primary bear foods, cutthroat trout (Oncorhynchus clarki), whitebark pine (Pinus albicaulis) nuts, and elk (Cervus elaphus), have declined in recent years. Because park managers and the public are concerned about the impact created by reductions in these foods, we quantified bear diets to determine how bears living near Yellowstone Lake are adjusting. We estimated diets using: 1) stable isotope and mercury analyses of hair samples collected from captured bears and from hair collection sites established along cutthroat trout spawning streams and 2) visits to recent locations occupied by bears wearing Global Positioning System collars to identify signs of feeding behavior and to collect scats for macroscopic identification of residues. Approximately 45 ± 22% ( ± SD) of the assimilated nitrogen consumed by male grizzly bears, 38 ± 20% by female grizzly bears, and 23 ± 7% by male and female black bears came from animal matter. These assimilated dietary proportions for female grizzly bears were the same as 10 years earlier in the Lake area and 30 years earlier in the Greater Yellowstone Ecosystem. However, the proportion of meat in the assimilated diet of male grizzly bears decreased over both time frames. The estimated biomass of cutthroat trout consumed by grizzly bears and black bears declined 70% and 95%, respectively, in the decade between 1997–2000 and 2007–2009. Grizzly bears killed an elk calf every 4.3 ± 2.7 days and black bears every 8.0 ± 4.0 days during June. Elk accounted for 84% of all ungulates consumed by both bear species. Whitebark pine nuts continue to be a primary food source for both grizzly bears and black bears when abundant, but are replaced by false-truffles (Rhizopogon spp.) in the diets of female grizzly bears and black bears when nut crops are minimal. Thus, both grizzly bears and black bears continue to adjust to changing resources, with larger grizzly bears continuing to occupy a more carnivorous niche than the smaller, more herbivorous black bear. © 2012 The Wildlife Society.