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Joseph D. Clark

Publications and source records attributed to Joseph D. Clark.

At least 37 records · Page 2Linked to original sources

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.

Tennessee, North Carolina↗

Survival and conflict behavior of American black bears after rehabilitation

Wildlife agencies face difficult situations when orphaned or injured American black bear ( Ursus americanus ) cubs (<12 months old) or yearlings (≥12 and <24 months old) are captured. One option is bear rehabilitation, the care and feeding of cubs or yearlings in a semi‐natural environment, followed by release. Unfortunately, the survival and movements of bears released from rehabilitation facilities are often poorly documented and the ultimate reasons for success or failure poorly understood. Our goal was to assess survival and post‐release conflict of orphaned bear cubs and yearlings following release from a rehabilitation facility, Appalachian Bear Rescue (ABR), in Townsend, Tennessee, USA, from 2015–2016. We predicted that rehabilitated bears would survive at similar rates, die from similar causes, and engage in similar conflict behavior to wild conspecifics. We equipped 42 black bear cubs and yearlings from ABR with global positioning system‐collars and released them in Great Smoky Mountains National Park or Cherokee National Forest, Tennessee and North Carolina, USA. Estimated annual survival using known‐fate methods for all released bears was 0.93 ± 0.06 [SE]). Survival for 13 bears released as cubs was 0.64 ± 0.14, whereas none of the bears released as yearlings died within 1 year after release ( n = 29). Survival of rehabilitated bears was similar to or higher than published rates for wild conspecifics. Three of 42 bears (7.1%) released from ABR engaged in conflict behavior up to 1 year following release, and those had spent time involved in conflict behavior with their mothers (e.g., approaching humans) prior to being orphaned. Despite not having the typical post‐natal experience with their mothers, the bears in our study appeared to behave and survive similarly to their wild conspecifics. Rehabilitation is effective for managing orphaned or injured bears. Best survival occurred for bears released as yearlings; however, managers can maximize cub survival through fall releases when plentiful wild foods are available.

North Carolina, Tennessee↗

Applying spatially explicit capture–recapture models to estimate black bear density in South Carolina

Population density is an important component of wildlife management decisions, but can be difficult to estimate directly for an itinerant, wide‐ranging species such as the American black bear ( Ursus americanus ). In South Carolina, USA, where there has been growth in black bear populations and bear–human‐conflict reports during the past several decades, managers need robust estimates of population size to inform management strategies. We used maximum‐likelihood capture–recapture models, using hair snares to collect DNA samples, to estimate density and abundance for a harvested population of black bear in northwestern South Carolina during 2013 to 2014. Models were tested in a spatially explicit framework using the secr package in Program R. Black bear density was estimated at 0.133 bears/km 2 (SE = 0.034) in 2013 and 0.179 bears/km 2 (SE = 0.043) in 2014. Black bear abundance in our study area was estimated to be 586 bears (SE = 95) in 2013 and 680 bears (SE = 128) in 2014, which are 2–3‐fold lower than previous estimates. We suggest that these estimates be considered a baseline for state biologists to employ in the population's management and in developing future harvest‐regulation strategies. Overall our study highlighted the potential for model choice to influence density estimates, and we concluded that spatially explicit models were appropriate for this study because geographic closure could not be assumed.

south Carolina↗

Comparing clustered sampling designs for spatially explicit estimation of population density

Spatially explicit capture–recapture methods do not assume that animals have equal access to sampling devices (e.g., detectors), which allows for gaps in the sampling extent and nonuniform (e.g., clustered) sampling designs. However, the performance (i.e., relative root mean squared error [RRMSE], confidence interval coverage, relative bias and relative standard error) of clustered detector arrays has not been thoroughly evaluated. I used simulations to evaluate the performance of various detector and cluster spacings, cluster configurations (i.e., number of detectors arranged in a square grid), sampling extents and number of sampling occasions for estimating population density, the relationship between detection rate and distance to a detector from the animal's center of activity ( σ ) and base detection rates, using American black bears ( Ursus americanus ) as a case study. My simulations indicated that a wide range of detector configurations can provide reliable estimates if spacing between detectors in clusters is ≥1 σ and ≤3 σ . A number of cluster configurations and occasion lengths produced estimates that were unbiased, resulted in good spatial coverage, and were relatively precise. Moreover, increasing the duration of sampling, establishing large study areas, increasing detection rates and spacing clusters so that cross‐cluster sampling of individuals can occur could help ameliorate deficiencies in the detector layout. These results have application for a wide array of species and sampling methods (e.g., DNA sampling, camera trapping, mark‐resight and search‐encounter) and suggest that clustered sampling can significantly reduce the effort necessary to provide reliable estimates of population density across large spatial extents that previously would have been infeasible with nonclustered sampling designs.

Population Ecology↗

Early genetic outcomes of American black bear reintroductions in the Central Appalachians, USA

Habitat loss and overexploitation extirpated American black bears (Ursus americanus) from most of the Central Appalachians, USA, by the early twentieth century. To attempt to restore bears to the southwestern portion of this region, 2 reintroductions that used small founder groups (n = 27 and 55 bears), but different release methods (hard versus soft), were conducted during the 1990s. We collected hair samples from black bears in the reintroduced Big South Fork (BSF) and Kentucky–Virginia populations (KVP), their respective Great Smoky Mountains (GSM) and Shenandoah National Park (SNP) source populations, and a neighboring population in southern West Virginia (SWV) to investigate the early genetic outcomes of bear reintroduction. Despite having undergone genetic bottlenecks, genetic diversity remained similar between reintroduced populations and their sources ~15 years after the founder events (ranges: AR = 4.86–5.61; HO = 0.67–0.75; HE = 0.65–0.71). Effective population sizes of the reintroduced KVP and BSF (NE = 31 and 36, respectively) were substantially smaller than their respective SNP and GSM sources (NE = 119 and 156, respectively), supporting founder effects. Genetic structure analysis indicated that the hard released (i.e., no acclimation period) KVP founder group likely declined considerably, whereas the soft released BSF founder group remained mostly intact, suggesting superior effectiveness of soft releases. Asymmetrical gene flow via immigration from the SWV has resulted in the KVP recovering from the initial founder group reduction. Sustained isolation, small NE, and small population size of the BSF may warrant continued genetic monitoring to determine if gene flow from neighboring populations is established or NE declines. For future bear reintroductions, we suggest managers consider sourcing founders from populations with high genetic diversity and soft-releasing bears to locales that are, if possible, within the dispersal capability of extant populations to mitigate the potential consequences of founder effects and isolation.

Central Appalachians↗

Restoring a forest icon: Could returning the American chestnut remodel our wildlife landscape?

Mother Nature was not making it easy. It was February 18, 2009, and winds were gusting, sleet was falling, and temperatures were hovering around 40° F. Our crew of 9 which consisted of personnel from the USDA Forest Service Southern Research Station, the Cherokee National Forest, and The University of Tennessee’s Tree Improvement Program, was attempting to establish the first test planting of American chestnuts ( Castanea dentata ) bred for resistance to an exotic fungal pathogen, the chestnut blight ( Cryphonectria parasitica ). With each hole dug and seedlings tamped into the ground, our hope was that we were one step closer to restoring an important wildlife food to eastern hardwood forests.

Alabama, Connecticut, Delaware, Georgia, Illinois,↗

Genetic diversity, effective population size, and structure among black bear populations in the Lower Mississippi Alluvial Valley, USA

Multiple small populations of American black bears Ursus americanus , including the recently delisted Louisiana black bear subspecies U. a. luteolus , occupy a fragmented landscape in the Lower Mississippi Alluvial Valley, USA (LMAV). Populations include bears native to the LMAV, bears translocated from Minnesota during the 1960s, and recently reintroduced and colonizing populations sourced from within the LMAV. We estimated population structure, gene flow, and genetic parameters important to conservation of small populations using genotypes at 23 microsatellite markers for 265 bears from seven populations. We inferred five genetic clusters corresponding to the following populations: White River and western Mississippi, Tensas River and Three Rivers, Upper Atchafalaya, Lower Atchafalaya, and Minnesota. Upper Atchafalaya was suggested as the product of Minnesota-sourced translocations, but those populations have since diverged, likely because of a founder effect followed by genetic drift and isolation. An admixture zone recently developed in northeastern Louisiana and western Mississippi between migrants from White River and Tensas River, resulting in a Wahlund effect. However, gene flow among most populations has been limited and considerable genetic differentiation accumulated (global F ST = 0.22), particularly among the three Louisiana black bear populations that existed when federal listing occurred. Consistent with previous bottlenecks, founder effects, and persisting isolation, all LMAV bear populations had low genetic diversity ( A R = 2.08–4.81; H E = 0.36–0.63) or small effective population size ( N E = 3–49). Translocating bears among populations as part of a regional genetic restoration program may help improve genetic diversity and increase effective population sizes.

Lower Mississippi Alluvial Valley↗

Estimating population extinction thresholds with categorical classification trees for Louisiana black bears

Monitoring vulnerable species is critical for their conservation. Thresholds or tipping points are commonly used to indicate when populations become vulnerable to extinction and to trigger changes in conservation actions. However, quantitative methods to determine such thresholds have not been well explored. The Louisiana black bear ( Ursus americanus luteolus ) was removed from the list of threatened and endangered species under the U.S. Endangered Species Act in 2016 and our objectives were to determine the most appropriate parameters and thresholds for monitoring and management action. Capture mark recapture (CMR) data from 2006 to 2012 were used to estimate population parameters and variances. We used stochastic population simulations and conditional classification trees to identify demographic rates for monitoring that would be most indicative of heighted extinction risk. We then identified thresholds that would be reliable predictors of population viability. Conditional classification trees indicated that annual apparent survival rates for adult females averaged over 5 years ( ) was the best predictor of population persistence. Specifically, population persistence was estimated to be ≥95% over 100 years when , suggesting that this statistic can be used as threshold to trigger management intervention. Our evaluation produced monitoring protocols that reliably predicted population persistence and was cost-effective. We conclude that population projections and conditional classification trees can be valuable tools for identifying extinction thresholds used in monitoring programs.

PLoS ONE↗

Genetic structure in Elk persists after translocation

Elk ( Cervus canadensis ) translocation success is thought to be facilitated by high post‐release herd cohesion and limited movements; both should ensure genetic mixing following release. Such mixing is important to reduce potential effects of inbreeding or genetic drift, which can be especially important in small founding populations. We had a natural experiment where we could evaluate genetic mixing of 2 distinct lineages of elk after translocation to the same area. Founding elk ultimately came from north and south of a road barrier at Elk Island National Park (EINPN or EINPS, respectively), Alberta, Canada and the 2 groups were genetically distinct. During 2000 to 2003, elk originating from Elk Island National Park were translocated to Cumberland Mountains, Tennessee (TNCM) and Great Smoky Mountains National Park, North Carolina (GSMNP), USA (some elk spent time at Land Between the Lakes Recreation Area, Kentucky, USA, before their final translocation). At TNCM, translocated elk were hard released, whereas at GSMNP elk were held in pens up to 60 days before release (i.e., soft release). We hypothesized that associations formed in the source population would affect genetic structure in the future population. We predicted that matrilineal groups would stay closer together and have similar movements after translocation. We used 16 microsatellite markers to analyze genetic composition and structure of translocated elk and their offspring in the years after release. Most source elk used for translocation strongly assigned to either EINPN or EINPS (93.2%, n = 204). Evaluating the genetic structure of offspring after translocation, we found the 2 genetic groups mostly persisted ≥11 years following release. We measured the Euclidean distance between all possible pairs of telemetered female elk during each season and year and calculated the maximum distance moved from the release sites for females surviving >1 year. Mean Euclidean distances between pairwise locations of female elk were similar for each genetic cluster for each area. The mean distances for all paired locations (genetic clusters combined) in TNCM were 14.67 km ( n = 4,576 ± 13.23 [SD]) and in GSMNP were 9.30 km ( n = 1,468 ± 9.75). However, when looking at only simultaneous locations <50 m apart, the frequency of occurrence was higher ( P < 0.001) for elk with the same genetic structure (71.1%) compared with those with different structure (28.9%). The maximum distance travelled from the release site was not different for the 2 genetic groups, but EINPN females tended to travel farther. Pairwise female distances were lower in GSMNP where we used a soft release. Release methodology and social structure appear to affect movements and possibly genetic mixing after translocation. Given that restoration success can depend on maintaining genetic diversity and number of founders, our analyses suggest that within‐cluster breeding bias can result in lower genetic variability and a smaller effective population size than previously assumed.

Kentucky, Tennessee↗

Elk research efforts

Presented the history of the NC elk herd and summarized early research to determine the population dispersal and mortality rates, assess habitat use, and evaluate elk’s impact on the national park to estimate the probability of success in establishing a permanent elk population in the Great Smoky Mountains National Park (GSMNP). Gave an overview of a fiveyear elk population study beginning October 2018

Report↗

No flood effect on recruitment of a small Louisiana black bear population

A flood event in 2011 had minor impacts on apparent survival and movement probabilities of a small, isolated population of Louisiana black bears ( Ursus americanus luteolus ) in the Upper Atchafalaya River Basin, Louisiana, USA. However, the potential effects of the flood on recruitment of juveniles into the population, then listed as threatened under the United States Endangered Species Act, were not evaluated. We used hair trapping data collected from 2007 to 2015 and Pradel temporal symmetry models in a robust‐design framework to investigate changes in per capita recruitment that could have resulted from the flood. We detected 91 bears (37 M:54 F) within the flooded area during our study period, ranging from 21 to 44 individuals/year. Models that tested for reduced recruitment resulting from the flood were not supported more than models with constant recruitment, and the population growth rate did not decline. Although we documented marginally lower recruitment following the 2011 flood, lag effects and detectability biases complicated our analysis. We suggest that wildlife managers continue monitoring recruitment and survival in this recently delisted black bear population given the potential for heightened flood frequency and severity in the future.

Journal of Wildlife Management↗

Spatially explicit population estimates for black bears based on cluster sampling

We estimated abundance and density of the 5 major black bear ( Ursus americanus ) subpopulations (i.e., Eglin, Apalachicola, Osceola, Ocala-St. Johns, Big Cypress) in Florida, USA with spatially explicit capture-mark-recapture (SCR) by extracting DNA from hair samples collected at barbed-wire hair sampling sites. We employed a clustered sampling configuration with sampling sites arranged in 3 × 3 clusters spaced 2 km apart within each cluster and cluster centers spaced 16 km apart (center to center). We surveyed all 5 subpopulations encompassing 38,960 km 2 during 2014 and 2015. Several landscape variables, most associated with forest cover, helped refine density estimates for the 5 subpopulations we sampled. Detection probabilities were affected by site-specific behavioral responses coupled with individual capture heterogeneity associated with sex. Model-averaged bear population estimates ranged from 120 (95% CI = 59–276) bears or a mean 0.025 bears/km 2 (95% CI = 0.011–0.44) for the Eglin subpopulation to 1,198 bears (95% CI = 949–1,537) or 0.127 bears/km 2 (95% CI = 0.101–0.163) for the Ocala-St. Johns subpopulation. The total population estimate for our 5 study areas was 3,916 bears (95% CI = 2,914–5,451). The clustered sampling method coupled with information on land cover was efficient and allowed us to estimate abundance across extensive areas that would not have been possible otherwise. Clustered sampling combined with spatially explicit capture-recapture methods has the potential to provide rigorous population estimates for a wide array of species that are extensive and heterogeneous in their distribution.

Florida↗

Northern bobwhite breeding season ecology on a reclaimed surface mine

Surface coal mining and subsequent reclamation of surface mines have converted large forest areas into early successional vegetative communities in the eastern United States. This reclamation can provide a novel opportunity to conserve northern bobwhite ( Colinus virginianus ). We evaluated the influence of habitat management activities on nest survival, nest-site selection, and brood resource selection on managed and unmanaged units of a reclaimed surface mine, Peabody Wildlife Management Area (Peabody), in west-central Kentucky, USA, from 2010 to 2013. We compared resource selection, using discrete-choice analysis, and nest survival, using the nest survival model in Program MARK, between managed and unmanaged units of Peabody at 2 spatial scales: the composition and configuration of vegetation types (i.e., macrohabitat) and vegetation characteristics at nest sites and brood locations (i.e., microhabitat). On managed sites, we also investigated resource selection relative to a number of different treatments (e.g., herbicide, disking, prescribed fire). We found no evidence that nest-site selection was influenced by macrohabitat variables, but bobwhite selected nest sites in areas with greater litter depth than was available at random sites. On managed units, bobwhite were more likely to nest where herbicide was applied to reduce sericea lespedeza ( Lespedeza cuneata ) compared with areas untreated with herbicide. Daily nest survival was not influenced by habitat characteristics or by habitat management but was influenced by nest age and the interaction of nest initiation date and nest age. Daily nest survival was greater for older nests occurring early in the breeding season (0.99, SE < 0.01) but was lower for older nests occurring later in the season (0.08, SE = 0.13). Brood resource selection was not influenced by macrohabitat or microhabitat variables we measured, but broods on managed units selected areas treated with herbicide to control sericea lespedeza and were located closer to firebreaks and disked native-warm season grass stands than would be expected at random. Our results suggest the vegetation at Peabody was sufficient without manipulation to support nesting and brood-rearing northern bobwhite at a low level, but habitat management practices improved vegetation for nesting and brood-rearing resource selection. Reproductive rates (e.g., nest survival and re-nesting rates) at Peabody were lower than reported in other studies, which may be related to nutritional deficiencies caused by the abundance of sericea lespedeza. On reclaimed mine lands dominated by sericea lespedeza, we suggest continuing practices such as disking and herbicide application that are targeted at reducing sericea lespedeza to improve the vegetation for nesting and brood-rearing bobwhite.

Kentucky↗

A long-term evaluation of biopsy darts and DNA to estimate cougar density

Accurately estimating cougar ( Puma concolor ) density is usually based on long-term research consisting of intensive capture and Global Positioning System collaring efforts and may cost hundreds of thousands of dollars annually. Because wildlife agency budgets rarely accommodate this approach, most infer cougar density from published literature, rely on short-term studies, or use hunter harvest data as a surrogate in their jurisdictions; all of which may limit accuracy and increase risk of management actions. In an effort to develop a more cost-effective long-term strategy, we evaluated a research approach using citizen scientists with trained hounds to tree cougars and collect tissue samples with biopsy darts. We then used the DNA to individually identify cougars and employed spatially explicit capture–recapture models to estimate cougar densities. Overall, 240 tissue samples were collected in northeastern Washington, USA, producing 166 genotypes (including recaptures and excluding dependent kittens) of 133 different cougars (8-25/yr) from 2003 to 2011. Mark–recapture analyses revealed a mean density of 2.2 cougars/100 km 2 (95% CI=1.1-4.3) and stable to decreasing population trends (β=-0.048, 95% CI=-0.106–0.011) over the 9 years of study, with an average annual harvest rate of 14% (range=7-21%). The average annual cost per year for field sampling and genotyping was US$11,265 ($422.24/sample or $610.73/successfully genotyped sample). Our results demonstrated that long-term biopsy sampling using citizen scientists can increase capture success and provide reliable cougar-density information at a reasonable cost.

Washington↗

Demographic rates and population viability of black bears in Louisiana

The Louisiana black bear ( Ursus americanus luteolus ) was reduced to a few small, fragmented, and isolated subpopulations in the Lower Mississippi Alluvial Valley by the mid-twentieth century resulting from loss and fragmentation of habitat. In 1992, the United States Fish and Wildlife Service (USFWS) granted the Louisiana black bear threatened status under the United States Endangered Species Act of 1973. Since that time, a recovery plan was developed, a reintroduced population was established, and habitat recovery has occurred. The Recovery Plan states that a minimum of 2 populations must be viable (i.e., persistence probabilities over 100 years >0.95), 1 in the Tensas River Basin and 1 in the Atchafalaya River Basin. Consequently, our objectives were to 1) estimate demographic rates of Louisiana black bear subpopulations, 2) develop data-driven stochastic population projection models, and 3) determine how different projection model assumptions affect population trajectories and predictions about long-term persistence. Our overall goal was to assess long-term persistence of the bear subpopulations in Louisiana, individually and as a whole. We collected data using varying combinations of non-invasive DNA sampling, live capture, winter den visits, and radio monitoring from 2002 to 2012 in the 4 areas currently supporting breeding subpopulations in Louisiana: Tensas River Basin (TRB), Upper Atchafalaya River Basin (UARB), Lower Atchafalaya River Basin (LARB), and a recently reintroduced population at the Three Rivers Complex (TRC). From 2002 to 2012, we radio monitored fates of 86 adult females within the TRB and 43 in the TRC. Mean estimates of annual adult survival for the TRB and TRC were 0.997 and 0.990, respectively, when unknown fates were assumed alive and 0.970 and 0.926 when unknown fates were assumed dead. From 2003 to 2013, we observed 130 cub litters from 74 females in the TRB, and 74 cub litters from 45 females in the TRC. During the same period, we observed 43 yearling litters for 33 females in the TRB and 21 yearling litters for 19 females in the TRC. The estimated number of cubs and number of yearlings produced per breeding adult female was 0.47 and 0.20, respectively, in the TRB and 0.32 and 0.18 in the TRC. On the basis of matrix projection models, asymptotic growth rates ranged from 1.053 to 1.078 for the TRB and from 1.005 to 1.062 for the TRC, depending on how we treated unresolved fates of adult females. Persistence probabilities estimated from stochastic population models based on telemetry data ranged from 0.997 to 0.998 for the TRC subpopulation depending on model assumptions and were >0.999 for the TRB regardless of model assumptions. We extracted DNA from hair collected at baited, barbed-wire enclosures in the TRB, UARB, and LARB to determine individual identities for capture-mark-recapture (CMR) analysis. We used those detection histories to estimate apparent survival ( φ ), per-capita recruitment ( f ), abundance ( N ), realized growth rate ( λ ), and long-term viability, based on Bayesian hierarchical modeling methods that allowed estimation of temporal process variance and parameter uncertainty. Based on 23,312 hair samples, annual N for females in the TRB ranged from 133 to 164 during 2006–2012, depending on year and how detection heterogeneity was modeled. Geometric mean of λ ranged from 0.996 to 1.002. In the UARB, we collected 11,643 hair samples from 2007 to 2012, from which estimates of N for females ranged from 23 to 43 during the study period, depending on detection heterogeneity model. The geometric mean of λ ranged from 1.038 to 1.059. Estimated N for females in LARB ranged from 69 to 96, and annual λ ranged from 0.80 to 1.11 based on 3,698 hair samples collected during 2010–2012, also depending on year and heterogeneity model. Probabilities of persistence over 100 years for the TRC and TRB based on stochastic matrix projection models that used vital rate estimates from telemetry data were >0.95 for all scenarios. Probability of persistence at the TRB and the UARB based on projection models that used vital rate estimates from CMR analyses ranged from 0.928 to 0.954 and from 0.906 to 0.959, respectively, depending on model assumptions. Data from the LARB were insufficient for a viability assessment. Thus, individual persistence probabilities for TRB and UARB did not meet the strict definition of viability (i.e., >0.95) under some model assumptions. However, the joint probability of bears persisting either in the TRB or UARB was >0.993 assuming individual population dynamics were independent and was >0.958 assuming dynamics were perfectly correlated. Furthermore, including the TRC increased the joint probability of bears persisting somewhere in the TRB, UARB, or TRC to >0.999 based on the most pessimistic individual persistence estimates from those subpopulations. Therefore, if the intent of specifying that 2 subpopulations should be viable was to ensure the persistence of Louisiana black bears somewhere within its historical range, then the viability threshold was met. © 2016 The Wildlife Society.

Louisiana↗

Connectivity among subpopulations of Louisiana black bears as estimated by a step selection function

Habitat fragmentation is a fundamental cause of population decline and increased risk of extinction for many wildlife species; animals with large home ranges and small population sizes are particularly sensitive. The Louisiana black bear ( Ursus americanus luteolus ) exists only in small, isolated subpopulations as a result of land clearing for agriculture, but the relative potential for inter-subpopulation movement by Louisiana black bears has not been quantified, nor have characteristics of effective travel routes between habitat fragments been identified. We placed and monitored global positioning system (GPS) radio collars on 8 female and 23 male bears located in 4 subpopulations in Louisiana, which included a reintroduced subpopulation located between 2 of the remnant subpopulations. We compared characteristics of sequential radiolocations of bears (i.e., steps) with steps that were possible but not chosen by the bears to develop step selection function models based on conditional logistic regression. The probability of a step being selected by a bear increased as the distance to natural land cover and agriculture at the end of the step decreased and as distance from roads at the end of a step increased. To characterize connectivity among subpopulations, we used the step selection models to create 4,000 hypothetical correlated random walks for each subpopulation representing potential dispersal events to estimate the proportion that intersected adjacent subpopulations (hereafter referred to as successful dispersals). Based on the models, movement paths for males intersected all adjacent subpopulations but paths for females intersected only the most proximate subpopulations. Cross-validation and genetic and independent observation data supported our findings. Our models also revealed that successful dispersals were facilitated by a reintroduced population located between 2 distant subpopulations. Successful dispersals for males were dependent on natural land cover in private ownership. The addition of hypothetical 1,000-m- or 3,000-m-wide corridors between the 4 study areas had minimal effects on connectivity among subpopulations. For females, our model suggested that habitat between subpopulations would probably have to be permanently occupied for demographic rescue to occur. Thus, the establishment of stepping-stone populations, such as the reintroduced population that we studied, may be a more effective conservation measure than long corridors without a population presence in between.

Louisiana↗