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Joseph D. Clark

Publications and source records attributed to Joseph D. Clark.

At least 19 recordsLinked to original sources

Northern bobwhites select for native grasses on working grazing land

Northern bobwhite ( Colinus virginianus ; bobwhite) populations have experienced an 85% decline across most of its range since the 1960s. The most drastic decreases have been in the southeastern United States where biologists attribute the decline to widespread habitat loss, including conversion of native grasslands to tall fescue ( Lolium arundinaceum ) and other exotic cool-season grass (CSG) pasture and hayfields. Including agricultural lands in conservation programs could improve habitat conditions on a regional scale. One working-lands conservation strategy involves the use of native warm-season grasses (NWSGs) rather than cool-season exotic grasses as economically viable cattle forage. To evaluate this management practice for creating bobwhite habitat, we conducted a field study on a bobwhite population in eastern Kentucky, USA, where grazed NWSG and burned NWSG fields were adjacent to exotic grazed and exotic hayed CSG fields. Between April 2019 and October 2022, we used radio telemetry to track bobwhites to evaluate resource selection at second- and third-order scales. Bobwhites used traditionally managed CSGs less than would be expected by chance at the second-order scale in both breeding and non-breeding seasons. Bobwhite use of grazed NWSG and burned NWSG was greater than would be expected by chance at the second-order scale in both breeding and non-breeding seasons. Similarly, at the third-order scale, bobwhites used CSGs less than would be expected by chance, whereas NWSGs and woody stems were used more than by chance alone. Our study suggests that bobwhites select NWSGs at multiple spatial scales despite broad-scale availability of managed exotic CSGs. Under a working-lands framework, the integration of NWSGs into working lands could create bobwhite habitat in the southeastern United States, especially if woody stems are present.

Kentucky↗

Effectiveness of black bear translocation as a conflict management tool

Great Smoky Mountains National Park (GRSM) in Tennessee and North Carolina, USA, has a high-density American black bear ( Ursus americanus ) population and high human visitation, resulting in frequent human–bear conflicts. Translocation is a common tool for conflict mitigation, but previous research at GRSM based on very high frequency (VHF) telemetry and eartag returns found that the fates of most translocated conflict bears were unknown, thereby leaving many unanswered questions about the fates and movements of translocated bears, including their propensity for engaging in recurrent human–bear conflicts. We equipped 50 bears involved in human–bear conflicts in GRSM with global positioning system (GPS) radio-collars and translocated them to Cherokee National Forest, Tennessee. We used those GPS location data to evaluate survival, recurrence of conflict activity, homing rate, and settling rate. Many of these bears were released in the Pigeon River gorge (PRG), where we also collared 37 resident bears to compare survival rates and movement patterns. Known-fate models indicated that the mean annual survival probability for translocated bears across the study area during all years (2015–2024) was 0.223 (95% CI = 0.107–0.339), whereas the survival of translocated bears and resident bears in the PRG during years 2022–2024 was 0.210 (95% CI = 0.000–0.445) and 0.787 (95% CI = 0.632–0.942), respectively. Annual survival of translocated bears was also lower (0.034, 95% CI = 0.000–0.125) than their non-translocated counterparts that remained in GRSM (0.869, 95% CI = 0.762–0.976) from 2015–2018. Harvest was the greatest overall mortality risk for all translocated bears (0.482, 95% CI = 0.326–0.638), and translocated bears were at greater risk of harvest (0.750, 95% CI = 0.350–1.000) than residents (0.136, 95% CI = 0.000–0.280) in the PRG. The annual probability of translocated bears returning to their original capture locations (i.e., homing) decreased with distance translocated and averaged 0.615 (95% CI = 0.341–0.889) for adults and 0.111 (95% CI = 0.000–0.318) for subadults. For every 1-km increase in distance translocated, the weekly odds of a bear homing decreased by a factor of 0.975 ( ̂𝛽 = −0.025, 85% CI = −0.046 to −0.004). The annual probability of recurrent conflict for translocated bears, defined as a report to agency officials by landowners, was 0.388 (95% CI = 0.190–0.586). Recurrent conflict increased with the level of food conditioning ( ̂𝛽 = 0.334, 85% CI = 0.098–0.570). Public education and improved waste management are paramount to prevent human–bear conflicts, as translocation and other bear-centered options may not accomplish desired outcomes.

North Carolina, Tennessee↗

Comparison of methods for estimating wild turkey poult survival

Eastern wild turkey ( Meleagris gallopavo silvestris ) population growth is driven by variation in reproduction, and poult survival is a crucial vital rate. Traditional poult survival monitoring uses flush counts of radio-tagged females, but brood flocking (when broods and females merge into larger flocks) and mark retention are potential problems with this method and can produce biased estimates. Alternatively, radio-tagging poults to estimate survival offers a potentially less-biased method if tagging and tracking poults can be conducted without adverse effects on the poults. We compared poult survival estimates derived from flush counts and from radio-tagged poults over a 56-day monitoring period during 2018–2022 in south-central Tennessee, USA. We radio-tagged 183 poults and monitored 85 broods via 2-week flush counts and observed 572 individual poults during flush counts over the 56-day monitoring period. We used known-fate survival models for the telemetry data, Lukacs survival models for the flush count data, and a modified known-fate model to estimate whether radio-tagging poults affected their survival. Two-week survival estimates from the flush count of broods, and radio-tagged poults were similar (flush count: day 0–28: 0.25, 95% CI: 0.20–0.31, day 29–56: 0.56, 95% CI: 0.36–0.76; radio-tagged: day 0–28: 0.30, 95% CI: 0.23–0.37, day 29–56: 0.68, 95% CI: 0.49–0.87). Using known-fate survival models, radio-tagged poults had similar survival rates to non-tagged poults within the brood (day 0–28: Ŝ Radio-tagged = 0.15, 95% CI: 0.10–0.20 v. Ŝ Non-tagged = 0.20, 95% CI: 0.16–0.23), which suggests the radio-tags did not directly affect survival. However, survival of individuals that were trapped was lower than survival of broods that were not trapped during the first 14 days. Trapping methods may need to be adjusted to limit incidental capture effects when choosing to use radio-tagged poults. Conducting flush counts every 14 days until day 56 of the brood-rearing period likely is the most cost-effective method for estimating poult survival. However, monitoring individual radio-tagged poults may yield additional information, such as cause-specific mortality, that may better inform management.

Tennessee↗

Spatially explicit capture-mark-recapture to evaluate demographic status of the Louisiana black bear

Louisiana black bears ( Ursus americanus luteolus ) occur in semi-isolated fragments of bottomland hardwood forest in the lower Mississippi Alluvial Valley and were listed as threatened under the United States Endangered Species Act in 1992. A population viability analysis based on radio-telemetry and capture-mark-recapture (CMR) data collected from 2002 to 2012 revealed that the probability of bears persisting in at least 1 subpopulation was >0.999, which prompted the United States Fish and Wildlife Service to remove the Louisiana black bear from the threatened species list in 2016. A post-delisting monitoring plan was developed, which included continued noninvasive CMR surveys to monitor subpopulation trends. We used genetic CMR data based on non-invasively collected hair samples for a post-delisting assessment of the demographic status of the black bear subpopulations in Louisiana, USA. The assessment included primary range in the Tensas River Basin (TRB; 2006–2020), the Upper Atchafalaya River Basin (UARB; 2007–2020), and the Three Rivers Complex (TRC; 2014 and 2021), where bears had been reintroduced beginning in 2001, and adjacent areas of possible range expansion (i.e., secondary range). We used spatially explicit closed-population capture-recapture models to estimate abundance ( N ), density ( D ), and the realized population growth rate ( λ ) for female bears at TRB, UARB, and TRC. Model-averaged estimates of N for primary range at TRB ranged from 135 (95% CI = 121–149) female bears in 2006 to 140 (95% CI = 123–157) in 2020 with mean λ of 1.003 (95% CI = 0.991–1.015), which suggested a stable primary population. An estimated 56 (95% CI = 19–92) additional female bears occurred in secondary range at TRB in 2020. Model-averaged estimates of N for primary range at UARB ranged from 35 (95% CI = 28–43) females in 2007 to 33 (95% CI = 28–43) in 2020, with mean λ = 0.996 (95% CI = 0.972–1.020), again suggesting a stable population. We estimated 3 (95% CI = 0–6) additional female bears occurred in secondary range at UARB during 2020. The estimate of N at TRC was 28 (95% CI = 18–44) females in 2014 and 42 (95% CI = 19–94) in 2021. The number of bears in the secondary ranges suggests some bears may have emigrated from the primary areas and colonized secondary areas, likely facilitated by increases in bottomland hardwood forests adjacent to the core populations. The stable primary populations, the reintroduced population at TRC, and the number of bears in secondary range adjacent to TRB indicate the overall number of Louisiana black bears has increased since monitoring began.

Louisiana↗

Spatially explicit capture-recapture using fecal DNA to estimate elk population abundance and growth in western North Carolina, USA

In an effort to restore extirpated elk to their historical range, 52 elk were reintroduced to Great Smoky Mountains National Park (GRSM) in North Carolina, USA, during 2001 and 2002. Since their reintroduction, elk numbers have increased, and elk have extended their range beyond GRSM boundaries. We used spatially explicit capture-recapture (SCR) methods based on fecal DNA to identify individual elk and estimate population abundance ( N ), apparent survival ( φ ), per capita recruitment ( f ), and population growth rate ( λ ) in western North Carolina. We walked a series of transects during 3 winter field seasons (2020–2022) and collected elk pellets encountered along those transects. We created spatially explicit capture histories and incorporated those data into both closed and open population SCR models. The top performing closed SCR models for males and females estimated density by year and as a function of the scaled distance to the nearest field, with densities decreasing as the distance increased. Combined male and female N were 179 elk (95% CI = 149–215) in 2020, 220 elk (95% CI = 188–256) in 2021, and 240 elk (95% CI = 207–279) in 2022. The top open population model estimated both φ and λ as functions of sex and year. The estimate of φ for males was 0.682 (95% CI = 0.317–0.908) during 2020–2021 and 0.339 (95% CI = 0.152–0.596) during 2021–2022 and for females was 0.953 (95% CI = 0.830–1.000) during 2020–2021 and 0.829 (95% CI = 0.601–1.000) during 2021–2022. The annual population growth rate ( λ ) for males was 1.127 (95% CI = 0.806–1.575) during 2020–2021 and 0.811 (95% CI = 0.566–1.163) during 2021–2022 and for females was 1.559 (95% CI = 1.162–2.091) during 2020–2021 and 1.122 (95% CI = 0.876–1.437) during 2021–2022. Our elk abundance estimates in areas >300 m from fields were negligible, and we suggest that sampling only the areas in and adjacent to fields in the future will result in reliable but more cost-efficient population estimates. Confidence intervals for vital rate parameters were wide for our 3-year dataset, but continued annual pellet sampling will increase sample sizes for vital rate estimation and thus improve precision. If elk herd expansion on public lands is desired, we suggest habitat modification to establish open grasslands adjacent to forests.

North Carolina↗

Assessing wild turkey productivity before and after a 14-day delay in the start date of the spring hunting season in Tennessee

Ten state wildlife management agencies in the United States, including six within the Southeast, have delayed their spring wild turkey ( Meleagris gallopavo ) hunting seasons since 2017 by five or more days to address concerns related to the potential effects of hunting on wild turkey seasonal productivity. One hypothesis posits that if the spring hunting season is too early, there may be insufficient time for males to breed hens before being harvested, thus leading to reduced seasonal productivity. We conducted an experiment to determine whether delaying the wild turkey hunting season by 2 weeks in south-middle Tennessee would affect various reproductive rates. In 2021 and 2022, the Tennessee Fish and Wildlife Commission experimentally delayed the spring hunting season to open 14 days later than the traditional date (the Saturday closest to 1 April) in Giles, Lawrence, and Wayne counties. We monitored reproductive rates from 2017 to 2022 in these three counties as well as two adjacent counties, Bedford and Maury, that were not delayed. We used a Before-After-Control-Impact design to analyze the proportion of hens nesting, clutch size, hatchability, nest success, poult survival and hen survival with linear mixed-effect models and AIC model selection to detect relationships between the 14-day delay and reproductive parameters. We detected no relationship ( p > .05) between the 14-day delay and any individual reproductive parameter. In addition, recruitment (hen poults per hen that survived until the next breeding season) was very low (<0.5) and did not increase because of the 14-day delay. The traditional Tennessee start date had been in place since 1986 while the turkey harvest increased markedly until about 2006 and more recently stabilized. Our data indicate that moving the start of the hunting season from a period just prior to peak nest initiation to 2 weeks later, to coincide with a period just prior to peak nest incubation initiation, resulted in no change to productivity or populations in wild turkey flocks in south-middle Tennessee.

Tennessee↗

A systematic review of the effects of climate variability and change on black and brown bear ecology and interactions with humans

Climate change poses a pervasive threat to humans and wildlife by altering resource availability, changing co-occurrences, and directly or indirectly influencing human-wildlife interactions. For many wildlife agencies in North America, managing bears ( Ursus spp.) and human-bear interactions is a priority, yet the direct and indirect effects of climate change are exacerbating management challenges. Understanding the underlying ecological drivers of bear responses to climate variability and change, and the implications for conflict, will be critical for maintaining human-bear coexistence in North America. We synthesized 120 articles that identified direct and indirect mechanisms by which climate variability and change affect brown bears ( Ursus arctos ) and American black bears ( Ursus americanus ) in North America. The literature focused on examining climate impacts on bear diet, body size, habitat selection, space use, activity, denning chronology, and population demographics and dynamics. Across these categories, we summarized the documented and projected bear responses and resulting implications for human-bear interactions. Climate-driven changes in natural food availability were frequently implicated in influencing bear behavior and demography, and creating conditions under which interactions with humans are likely to increase. Bears in North America may face increased challenges as habitat and natural food availability continue to be altered by climate change. Our review provides a foundation upon which to identify climate drivers of bear ecology, conditions conducive to human-bear interactions, and adaptive management strategies. Given substantial evidence of climate impacts to bears, incorporating climate considerations into bear management can help managers strategically allocate resources and promote human-bear coexistence.

Biological Conservation↗

No long-term effect of black bear removal on elk calf recruitment in the southern Appalachians

In 2001 and 2002, 52 elk ( Cervus canadensis ; 21 males, 31 females), originally obtained from Elk Island National Park, Alberta, Canada, were transported and released into Cataloochee Valley in the northeastern portion of Great Smoky Mountains National Park (GRSM, Park), North Carolina, USA. The annual population growth rate ( λ ) was negative (0.996, 95% CI = 0.945–1.047) and predation by black bears ( Ursus americanus ) on elk calves was identified as an important determinant of population growth. From 2006 to 2008, 49 bears from the primary elk calving area (i.e., Cataloochee Valley) were trapped and translocated about 70 km to the southwestern portion of the Park just prior to elk calving. Per capita recruitment (i.e., the number of calves produced per adult female that survive to 1 year of age) increased from 0.306 prior to bear translocation (2001–2005) to 0.544 during years when bears were translocated (2006–2008) and λ increased to 1.118 (95% CI = 1.096–1.140). Our objective was to determine whether per capita calf recruitment rates after bear removal (2009–2019) at Cataloochee were similar to the higher rates estimated during bear removal (i.e., long-term response) or if they returned to rates before bear removal (i.e., short-term response), and how those rates compared with recruitment from portions of our study area where bears were not relocated. We documented 419 potential elk calving events and monitored 129 yearling and adult elk from 2001 to 2019. Known-fate models based on radio-telemetry and observational data supported calf recruitment returning to pre-2006 levels at Cataloochee (short-term response); recruitment of Cataloochee elk before and after bear relocation was lower (0.184) than during bear relocation (0.492). Recruitment rates of elk outside the removal area during the bear relocation period (0.478) were similar to before and after rates (0.420). In the Cataloochee Valley, cause-specific annual calf mortality rates due to predation by bears were 0.319 before, 0.120 during, and 0.306 after bear relocation. In contrast, the cause-specific annual mortality rate of calves in areas where bears were not relocated was 0.033 after the bear relocation period, with no bear predation on calves before or during bear relocation. The mean annual population growth rate for all monitored elk was 1.062 (95% CI = 0.979–1.140) after bear relocation based on the recruitment and survival data. Even though the effects of bear removal were temporary, the relocations were effective in achieving a short-term increase in elk recruitment, which was important for the reintroduction program given that the elk population was small and vulnerable to extirpation.

North Carolina↗

A multi-level modeling approach to guide management of female feral hogs in Great Smoky Mountains National Park

We trapped, anesthetized, and fit 16 female feral swine ( Sus scrofa ) with Global Positioning System (GPS) collars in Great Smoky Mountains National Park (GRSM) to develop predictive summer and winter models for more effective population control efforts. Given the highly diverse habitat and topography in GRSM and the spatial extent of our dataset, we employed Step Selection Function (SSF) to evaluate resource selection at the 3 rd -order level and Resource Selection Function (RSF) models at the 2 nd -order level for both summer and winter seasons. The summer SSF and RSF models suggested relatively similar levels of selection, whereas the winter models differed by method. We created a straightforward consensus model to better visualize the agreement and constraints of each set of models. In summer, feral swine used lower slopes regardless of elevation, especially those closer to human-dominated spaces such as along paved and gravel roadways. In winter, feral swine maintained preference for lower slopes but preferred oak-dominated forest areas and selection for human development was less than in summer. Wildlife managers can use these models to better focus feral swine surveillance and management in GRSM. Managers can identify areas of high use by season and plan control activities that are both accessible and highly efficient. The combination and consensus framework presented here can be applied to other systems where species’ habitat selection may result in incongruous results across different levels of selection or seasons of interest.

Tennessee↗

Density, harvest rates, and growth of a reintroduced American black bear population

Less than 30% of all species reintroductions have been successful and it is important that factors associated with success or failure be identified. Officials experimentally translocated 14 adult female American black bears ( Ursus americanus ) from Great Smoky Mountains National Park, North Carolina and Tennessee, USA, to Big South Fork National River and Recreation Area in the Cumberland Plateau of Kentucky and Tennessee, USA, in 1996–1997. Since that time, the reintroduced bear population has continued to expand in size and range so our study objective was to use spatially explicit capture-recapture methods across a wide spatial extent to estimate bear population abundance and growth. We constructed 440 (223 in KY, 217 in TN) hair traps in our primary sampling area in 2019 arranged in clusters of 4–9 traps/cluster, which we augmented with data from 138 hair traps in a secondary sampling area in Tennessee collected in 2018. We extracted and genotyped DNA from hair samples to construct spatially explicit capture histories, using spatial covariates to model inhomogeneous densities. Population abundance estimates across our 36,035-km 2 study area were 411 males and 406 females excluding cubs. Based on an initial standing population of 18 adult and subadult bears, the mean annual growth rate ( λ ) from 1998 to 2019 was 1.199. The mean annual harvest rate in Kentucky from 2013 to 2019 was 5.1% and in Tennessee from 2014 to 2019 was 13.2%. Based on simulations, the hunting seasons reduced mean λ from 1.217 to 1.199, but growth was rapid despite harvest. Genetic diversity was retained, with similar expected heterozygosity as in the source population. The lack of conspecifics, highly productive habitat, and an initial age and sex distribution that was skewed toward the most fecund members of the population likely contributed to the rapid growth and high levels of gene retention in this bear population.

Kentucky, Tennessee↗

Rainforest carnivore ecology in a managed forest reserve: Differential seasonal correlates between habitat components and relative abundance

Studies of relationships between seasons and Neotropical carnivore distributions tend to focus on water and prey availability without considering other habitat components such as escape, foraging, and resting cover. Our goal was to evaluate habitat characteristics that may be important for predicting the seasonal (dry or rainy) relative abundance of four commonly captured Neotropical carnivores (i.e., jaguar [ Panthera onca ], puma [ Puma concolor ], ocelot [ Leopardus pardalis ], and grey fox [ Urocyon cinereoargenteus ]) in Chiquibul Forest Reserve in Belize, Central America. We used trail camera data and random-effect Poisson models to investigate how prey ratios (number of prey detections/total detections), cover (e.g., logs and stumps used for hiding cover from predators), vegetation structure, and environmental site characteristics (e.g., site harvest-history, slope, aspect) were related to carnivore relative abundance. Both prey ratios and vegetation structure appeared in supported models more frequently than other environmental site characteristics and were negatively correlated with carnivore relative abundance. Supported models differed for each season for all species except jaguars for which mammalian prey ratios and prey cover at sites was always negatively correlated with jaguar relative abundance. Carnivores appeared to avoid sites where vegetation created ideal escape and hiding cover for prey even though prey may be less abundant. Our data suggest that vegetation structure and composition can create conditions conducive to carnivore foraging and that these characteristics can differ by season in the tropics.

Biological Conservation↗

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 km 2 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/km 2 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.

Georgia, North Carolina, South Carolina, Tennessee↗

Evaluation of connectivity among black bear populations in Georgia

Habitat fragmentation and loss contribute to isolation of wildlife populations and increased extinction risks for various species, including many large carnivores. We studied a small and isolated population of American black bears ( Ursus americanus ) that is of conservation concern in central Georgia, USA (i.e., central Georgia bear population [CGBP]). Our goal was to evaluate the potential for demographic and genetic interchange from neighboring bear populations to the CGBP. To evaluate resource selection and movement potential, we used 35,487 global positioning system locations collected every 20 minutes from 2012 to 2014 from 33 male bears in the CGBP. We then developed a step selection function model based on conditional logistic regression. Male bears chose steps that avoided crops, roads, and human developments and were closer to forests and woody wetlands than expected based on availability. We used a geographic information system to simulate 300 bear movement paths from nearby bear populations in northern Florida, northern Georgia, and southern Georgia to estimate the potential for immigration to the CGBP. Only 4 simulated movement paths from the nearby populations intersected the CGBP. The creation of a hypothetical 1-km-wide corridor between the southern Georgia population and the CGBP produced only minor improvements in interchange. Our findings suggest that demographic connectivity between the CGBP and surrounding bear populations may be limited, and coupled with previous works showing genetic isolation in the CGBP, that creation of corridors may have only marginal effects on restoring gene flow, at least in the near term. Management actions such as translocation and the establishment of stepping stone populations may be needed to increase the genetic diversity and demographic stability of bears in the CGBP. © 2021 The Wildlife Society.

Florida Georgia, North Carolina, South Carolina↗

American Black Bear (Ursus americanus)

American black bears (Ursus americanus) are endemic to North America, having speciated from other ursids some 1.2 to 1.8 million years ago (Kurtn & Anderson 1994). During that time, black bears came to occupy nearly all of the forested areas of the North American continent. Historically, black bears were one of the most important mammals to indigenous peoples of North America by providing food, fat, hides, and tools (Raybourne 1987). Bears also played important roles in indigenous culture as symbols of strength, hard work, and love (see Rockwell 1991). In the 18th and 19th centuries in the U.S., Canada, and Mexico, European settlers with firearms reduced black bear numbers (Williams 1930), but the axe and plow had equally negative effects on bear populations as forests gave way to agriculture and livestock. Black bears also faced intense pressure from unregulated market hunting, poaching, and predator control programs. Black bears disappeared from large portions of their North American range, being relegated to swamps, thickets, rugged mountains, and other areas deemed too inaccessible, unsuitable, or undesirable to be occupied by humans (Pelton & van Manen 1994). In the early 20th century, Canadian and U.S. governments established national parks, forests, and refuges, and state and provincial legislatures created wildlife management agencies and enacted regulations to manage wildlife populations. By the late 20th century, the combination of public land infrastructure, habitat improvements, harvest regulations, law enforcement, and information-education programs resulted in significant increases in black bear numbers and range expansions in the U.S. and Canada (Pelton & van Manen 1994), aided in no small part by the remarkable adaptability of this animal (Pelton 2003; Scheick & McCown 2014). Today, the American black bear is one of the most iconic, abundant, and economically important bear species in the world. Unfortunately, black bear populations in Mexico have not recovered similarly to those in the U.S and Canada, and the status of the species there is uncertain.

Book chapter↗

Spatial ecology and resource selection of eastern box turtles

Eastern box turtles ( Terrapene carolina carolina ) are widely distributed throughout the eastern United States. Although once common throughout much of its distribution, the species has experienced declines in local populations. Understanding resource selection is important for the conservation of this species; however, few data exist on resource selection for eastern box turtles in the southeastern United States. We estimated home range and resource selection for 100 individual turtles in the Blue Ridge, Ridge and Valley, and Cumberland Plateau and Mountains physiographic regions in Tennessee, USA, from 2016 to 2018. We used step‐selection functions to investigate eastern box turtle resource selection during May–August 2017 and May–August 2018 at 2 spatial scales. We classified vegetation type, measured vegetation composition and structure, recorded time since fire, and measured coarse woody debris abundance at 1,225 used telemetry locations and 1,225 associated available points. Home range sizes averaged 9.3 ha ± 3.0 (SE) using minimum convex polygon analysis, 8.25 ha ± 2.88 using 95% kernel density analysis, and 1.50 ha ± 0.56 using 50% kernel density analysis. Box turtles selected areas with greater visual obstruction at the 0–0.25‐m level, greater amounts of 10‐hour and 100‐hour fuels (timelag categories used in fire‐danger ratings), and greater litter depths compared to available locations. Box turtles were more likely to select areas with greater cover of brambles and coarser woody debris and were less likely to select areas with less vegetation cover. Vegetation type and time since last fire did not affect selection. Our data suggest that management activities that encourage greater understory vegetation cover, greater visual obstruction at the 0–0.25‐m level, and greater bramble cover will enhance habitat quality for eastern box turtles.

Journal of Wildlife Management↗

Direct and indirect effects of fire on eastern box turtles

Prescribed fire is an increasingly important management tool for eastern deciduous forests, but relativity little is known about the direct effects of fire on the eastern box turtle ( Terrapene carolina carolina ). We used very high frequency (VHF) transmitters to monitor mortality, movement, and spatial ecology of 118 box turtles in response to 17 prescribed fires across 4 seasons and 3 sites in east Tennessee, USA, during 2016–2018. Annual survival of box turtles that experienced a prescribed fire event was lower (0.87 ± 0.04 [SE]) than turtles that did not (0.98 ± 0.01) and was negatively correlated with fire intensity, fire temperature the turtle experienced, and litter depth. All prescribed fire‐related mortalities occurred during the early (Apr–May, n = 5) or late growing season (Sep–Oct, n = 1). Fourteen percent of box turtles we captured exhibited damage to their carapace from previous fire events. Box turtles that survived prescribed fires were in microsites that did not burn, moved to unburned areas during the fire, or burrowed following ignition. Home range size was similar before and after burns and sinuosity of movements did not differ in burned or unburned areas. Our results indicate that though box turtles are susceptible to prescribed fire during their active season, they have behavioral and physical traits that reduce the direct effects of prescribed fire. Prescribed fire practitioners should be aware of the risks of fire, particularly during the active season. We suggest managers consider altering prescribed fire intensity, seasonality, and firing pattern to minimize risk of direct effects where box turtles are of concern.

Tennessee↗