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Joseph G. Yarkovich

Publications and source records attributed to Joseph G. Yarkovich.

4 recordsLinked to original sources

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

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

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