Density-Dependent Harvest Modeling for the Eastern Wild Turkey

Abstract Many current wild turkey (Meleagris gallopavo) harvest models assume density-independent population dynamics. We developed an alternative model incorporating both nonlinear density-dependence and stochastic density-independent effects on wild turkey populations. We examined model sensitivity to parameter changes in 5% increments and determined mean spring and fall harvests and their variability in the short term (3 yr) and long term (10 yr) from proportional harvesting under these conditions. In the long term, population growth rates were most sensitive to poult:female ratios and the form of density dependence. The nonlinear density-dependent effect produced a population that maximized yield at 40% carrying capacity. The model indicated that a spring or fall proportional harvest could be maximized for fall harvest rates between 0% and 13% of the population, assuming a 15% spring male harvest and 5% spring illegal female kill. Combined spring and fall harvests could be maximized at a 9% fall harvest, under the same assumptions. Variability in population growth and harvest rates increased uncertainty in spring and fall harvests and the probability of overharvesting annual yield, with growth rate variation having the strongest effect. Model simulations suggested fall harvest rates should be conservative (≤9%) for most management strategies.     

Weather conditions during hunting season affect the number of harvested roe deer (Capreolus capreolus)

Due to human‐induced climate and landscape changes, distribution and abundance of many ungulate species have increased worldwide. Especially in areas where natural predators are absent, hunting is the essential management tool for regulating ungulate populations. Therefore, understanding the factors associated with harvest rates is the first step toward an adaptive management approach. Weather influences hunter and ungulate behavior and thus presumably harvest, but how and which meteorological parameters are linked to harvest numbers have rarely been evaluated. We used nearly 65,000 “sit and wait” and driven hunt harvests of roe deer (Capreolus capreolus) in Bavaria, Germany, and weather data from 2008 to 2017 to test for factors affecting roe deer harvests (i.e., temperature, rain hours, wind speed, sunshine duration, snow depth, workdays vs. weekends, month) using zero‐inflated negative binomial mixed‐effect models. Our results reveal that, besides workdays, high temperatures and prolonged rain resulted in fewer harvested animals, whereas sunshine duration in summer and snow height in snow‐rich areas partially favored harvests during sitting hunts in summer and winter, respectively. The influence of wind speed varied over the course of the year. In summer and autumn, wind speed commonly had a negative effect, positively affecting harvests in winter in some regions. Daily harvest numbers decreased during the summer and autumn hunting periods (May till mid‐October), while they increased during the winter period (mid‐October till mid‐January). Interestingly, harvest success during driven hunts, which are planned well in advance and therefore take place largely independent of weather conditions, was similarly affected by the weather. This result suggests that the inferred weather influence is not only due to the hunters'' decisions but also due to deer behavior. Since many ungulate populations may further benefit from climate change, building an understanding of the relationship between hunting success and weather will aid adaptive ungulate management.     

Fort Peck paddlefish population survival and abundance in the Missouri River

Excessive fishing pressure can induce population declines or complete collapse of fisheries. Unless commercial and recreational fisheries for K-selected fishes, or those with slow growth and late maturation, are carefully managed, declines in abundance or fishery collapse is probable. Paddlefish Polyodon spathula,are a K-selected species that experienced historical declines in abundance as a result of habitat degradation and overfishing. Mark-recapture studies are well-suited for long-lived fishes by providing information on population density and vital rates. For sustainable commercial or recreational fisheries targeting species such as the paddlefish, managers require accurate estimates of population vital rates including survival, abundance, and exploitation. We used a Montana Fish, Wildlife & Parks (MFWP) mark-recapture dataset and modified Jolly-Seber (POPAN) models to estimate survival, recapture, probability of entry, and abundance of 8,518 tagged paddlefish over a 25-year period. With many supporting estimates including stable survival (0.92 for females, mean of 0.82 for males), low exploitation rates (means of 2.6% for females and 2.9% for males), and stable abundance estimates (25-year mean of 12,309 individuals for both sexes), the Fort Peck paddlefish population appears to be stable and well-managed over the past 25 years. Presently, this is the only study focused on paddlefish in North America that has estimated survival and abundance for both male and female paddlefish using contemporary analyses. This research provided a unique opportunity to highlight that the effort exerted by management agencies to collect long-term field data is extremely useful to our understanding of fish populations and management.     

Marten and fisher responses to fluctuations in prey populations and mast crops in the northern hardwood forest

Many forest tree species produce seed (mast) crops that are consumed by a variety of wildlife species and these pulsed resources may mediate interactions among predator and prey populations. In the northern hardwood forests of New York, we investigated interactions among mast production, prey abundance, and harvests of American martens (Martes americana) and fishers (Martes pennanti) during 1988–2009. Mast production for beech (Fagus grandifolia), sugar maple (Acer saccharum), and mountain ash (Sorbus americana) was synchronous and an alternate-year pattern in production was evident for most of the time series. We documented considerable temporal variation in summer small mammal relative abundance and our numerical response models received substantial support for 5 of the 8 species, indicating lagged responses to autumn mast crops. Trap response of martens to the autumn production of beech mast and mountain ash berries was immediate and numerical responses to the relative abundance of small mammal prey occurred during the preceding summer. The age structure of the marten harvest differed based on the dominant alternate-year pattern of summer prey relative abundance and autumn mast production (χ²₄ = 33.06, P < 0.001). The proportion of juvenile marten in the autumn harvest was 52% and 34% following summers when small mammal relative abundance was high and low, respectively and these differences resulted in a persistent cohort effect that was apparent until age 3.5. Trap response of fishers to the autumn production of beech mast was immediate and numerical responses to the relative abundance of Sciurid prey occurred during the preceding summer. Marten and fisher harvests fluctuated similarly among New York, Maine, and New Brunswick, which may indicate regional synchronization of mast crops and responses of martens and fishers to similar prey dynamics. A better understanding of how food availability influences demographic responses and trapping vulnerability of martens and fishers would aid our ability to manage harvests of these species on a sustained yield basis. © 2011 The Wildlife Society.     

Are Brazil nut populations threatened by fruit harvest?

Harvest of Brazil nuts from the large, iconic tree Bertholletia excelsa generates substantial income for smallholders, providing a strong incentive to conserve the mature forests where it grows. Although much previous work has focused on the impact of nut harvest on new seedling recruits into B. excelsa populations, the connection between harvest rates and long‐term population stability is still unclear. Moreover, there is additional uncertainty for Brazil nut management in terms of population response to climate change and other anthropogenic influences. We drew on 14 years of research in two sites in Acre, Brazil with different B. excelsa nut harvest intensities (39% and 81%), to produce stochastic and deterministic matrix population models which incorporated parameter uncertainty in vital rates. Adult abundance was projected to remain close to the current observed abundance or higher through the next 50 years. Elasticity analyses revealed that the asymptotic population growth rate (λ) was most sensitive to stasis vital rates in sapling, juvenile, and adult stages. Deterministic transition matrices calculated using diameter growth rates dependent on rainfall yielded average λ values around 1.0 under extreme high, extreme low, and average annual rainfall. While sustained high rates of Brazil nut harvest and climate change could potentially negatively impact B. excelsa populations, changes in human use of the forested landscape are more immediate concern. To reduce the risk of population decline, smallholders and managers of B. excelsa rich forests should focus on conservation of pre‐mature and mature individuals.     

Effects of Timber Harvests and Silvicultural Edges on Terrestrial Salamanders

Balancing timber production and conservation in forest management requires an understanding of how timber harvests affect wildlife species. Terrestrial salamanders are useful indicators of mature forest ecosystem health due to their importance to ecosystem processes and sensitivity to environmental change. However, the effects of timber harvests on salamanders, though often researched, are still not well understood. To further this understanding, we used artificial cover objects to monitor the relative abundance of terrestrial salamanders for two seasons (fall and spring) pre-harvest and five seasons post-harvest in six forest management treatments, and for three seasons post-harvest across the edge gradients of six recent clearcuts. In total, we recorded 19,048 encounters representing nine species of salamanders. We observed declines in mean encounters of eastern red-backed salamanders (Plethodon cinereus) and northern slimy salamanders (P. glutinosus) from pre- to post-harvest in group selection cuts and in clearcuts. However, we found no evidence of salamander declines at shelterwoods and forested sites adjacent to harvests. Edge effects induced by recent clearcuts influenced salamanders for approximately 20 m into the forest, but edge influence varied by slope orientation. Temperature, soil moisture, and canopy cover were all correlated with salamander counts. Our results suggest silvicultural techniques that remove the forest canopy negatively affect salamander relative abundance on the local scale during the years immediately following harvest, and that the depth of edge influence of clearcuts on terrestrial salamanders is relatively shallow (<20 m). Small harvests (<4 ha) and techniques that leave the forest canopy intact may be compatible with maintaining terrestrial salamander populations across a forested landscape. Our results demonstrate the importance of examining species-specific responses and monitoring salamanders across multiple seasons and years. Long-term monitoring will be necessary to understand the full impacts of forest management on terrestrial salamanders.     

Survival and Recovery Rate of Canada Geese Staging in Interior Alaska

Abstract: Lesser Canada geese (Branta canadensis parvipes) are indistinguishable from other subspecies of small Canada geese on the wintering grounds using current survey methods. Consequently, managers are unable to adequately measure their abundance. Without direct estimates of abundance, researchers often use estimates of vital rates that influence abundance (e.g., annual survival) to monitor potential impact of harvest on the population. Based on capture and re-sighting data records of 567 geese marked from 1994 through 1998, we calculated annual survival and recovery rates for different age and sex classes of white-cheeked geese staging in interior Alaska. We compared those survival and recovery rates with those of other neck-collared white-cheeked geese. The best approximating model allowed survival to vary by age class while holding Seber's recovery probability (r̂) constant over sex, age class, and time. We estimated annual survival to be 0.49 (SE = 0.05) for hatch-year geese and 0.68 (SE = 0.03) for after-hatch-year geese based on the weighted average of all models with a change in Akaike's Information Criterion adjusted for small sample size and lack of fit < 4. Estimates of annual survival of white-cheeked geese in this study are among the lowest and recovery estimates are among the highest for migratory populations of neck-collared geese. Low survival estimates of Canada geese in our study suggest that harvest rates may be higher than in many other populations. Surveys to estimate abundance or other population parameters such as reproductive success and recruitment are necessary to determine whether this population is self-sustaining. Furthermore, we recommend monitoring abundance and harvest of small white-cheeked geese east and west of the Cascade Mountain Range separately to better determine harvest pressure on white-cheeked geese wintering east of the Cascades.     

Individual heterogeneity in black brant survival and recruitment with implications for harvest dynamics

We examined individual heterogeneity in survival and recruitment of female Pacific black brant (Branta bernicla nigricans) using frailty models adapted to a capture–mark–recapture context. Our main objectives were (1) to quantify levels of heterogeneity and examine factors affecting heterogeneity, and (2) model the effects of individual heterogeneity on harvest dynamics through matrix models. We used 24 years of data on brant marked and recaptured at the Tutakoke River colony, AK. Multievent models were fit as hidden Markov chain using program E‐SURGE with an adequate overdispersion coefficient. Annual survival of individuals marked as goslings was heterogeneous among individuals and year specific with about 0.23 difference in survival between “high” (0.73)‐ and “low” (0.50)‐quality individuals at average survival probability. Adult survival (0.85 ± 0.004) was homogeneous and higher than survival of both groups of juveniles. The annual recruitment probability was heterogeneous for brant >1‐year‐old; 0.56 (±0.21) and 0.31 (±0.03) for high‐ and low‐quality individuals, respectively. Assuming equal clutch sizes for high‐ and low‐quality individuals and that 80% of offspring were in the same quality class as the breeding female resulted in reproductive values about twice as high for high‐quality individuals than low‐quality individual for a given class of individuals producing differential contributions to population growth among groups. Differences in reproductive values greatly increased when we assumed high‐quality individuals had larger clutch sizes. When we assumed that 50% of offspring were in the same quality class as their mothers and clutches were equal, differences in reproductive values between quality classes were greatly reduced or eliminated (breeders [BRs]). We considered several harvest scenarios using the assumption that 80% of offspring were in the same quality class as their mothers. The amount of compensation for harvest mortality declined as the proportion of high‐quality individuals in the harvest increased, as differences in clutch sizes between groups decreased and as the proportion of BRs in the harvest increased. Synthesis and applications. Harvest at the same proportional level of the overall population can result in variable responses in population growth rate when heterogeneity is present in a population. λ was <1.0 under every scenario when harvest rates were >10%, and heterogeneity caused as much as +2% difference in growth rates at the highest levels of proportional harvest for low‐quality individuals and the greatest differences in qualities between classes of individuals, a critical difference for a population with λ near 1.0 such as the brant. We observed less response in overall survival in the presence of heterogeneity because we did not observe heterogeneity in the annual survival of BRs. This analysis provides a comprehensive view of overall compensation at the population level and also constitutes the first example of a survival‐recruitment model with heterogeneity. Individual heterogeneity should be more explicitly considered in harvest management of vertebrates.     

Spatio-temporal variation in male white-tailed deer harvest rates in Pennsylvania: Implications for estimating abundance

The performance of 2 popular methods that use age-at-harvest data to estimate abundance of white-tailed deer is contingent on assumptions about variation in estimates of subadult (1.5 yr old) and adult (≥2.5 yr old) male harvest rates. Auxiliary data (e.g., estimates of survival or harvest rates from radiocollared animals) can be used to relax some assumptions, but unless these population parameters exhibit limited temporal or spatial variation, these auxiliary data may not improve accuracy. Unfortunately maintaining sufficient sample sizes of radiocollared deer for parameter estimation in every wildlife management unit (WMU) is not feasible for most state agencies. We monitored the fates of 397 subadult and 225 adult male white-tailed deer across 4 WMUs from 2002 to 2008 using radio telemetry. We investigated spatial and temporal variation in harvest rates and investigated covariates related to the patterns observed. We found that most variation in harvest rates was explained spatially and that adult harvest rates (0.36–0.69) were more variable among study areas than subadult harvest rates (0.26–0.42). We found that hunter effort during the archery and firearms season best explained variation in harvest rates of adult males among WMUs, whereas hunter effort during only the firearms season best explained harvest rates for subadult males. From a population estimation perspective, it is advantageous that most variation was spatial and explained by a readily obtained covariate (hunter effort). However, harvest rates may vary if hunting regulations or hunter behavior change, requiring additional field studies to obtain accurate estimates of harvest rates. © 2011 The Wildlife Society.     

Integrated Population Modeling of Black Bears in Minnesota: Implications for Monitoring and Management

Background

Wildlife populations are difficult to monitor directly because of costs and logistical challenges associated with collecting informative abundance data from live animals. By contrast, data on harvested individuals (e.g., age and sex) are often readily available. Increasingly, integrated population models are used for natural resource management because they synthesize various relevant data into a single analysis.

Methodology/Principal Findings

We investigated the performance of integrated population models applied to black bears (Ursus americanus) in Minnesota, USA. Models were constructed using sex-specific age-at-harvest matrices (1980–2008), data on hunting effort and natural food supplies (which affects hunting success), and statewide mark–recapture estimates of abundance (1991, 1997, 2002). We compared this approach to Downing reconstruction, a commonly used population monitoring method that utilizes only age-at-harvest data. We first conducted a large-scale simulation study, in which our integrated models provided more accurate estimates of population trends than did Downing reconstruction. Estimates of trends were robust to various forms of model misspecification, including incorrectly specified cub and yearling survival parameters, age-related reporting biases in harvest data, and unmodeled temporal variability in survival and harvest rates. When applied to actual data on Minnesota black bears, the model predicted that harvest rates were negatively correlated with food availability and positively correlated with hunting effort, consistent with independent telemetry data. With no direct data on fertility, the model also correctly predicted 2-point cycles in cub production. Model-derived estimates of abundance for the most recent years provided a reasonable match to an empirical population estimate obtained after modeling efforts were completed.

Conclusions/Significance

Integrated population modeling provided a reasonable framework for synthesizing age-at-harvest data, periodic large-scale abundance estimates, and measured covariates thought to affect harvest rates of black bears in Minnesota. Collection and analysis of these data appear to form the basis of a robust and viable population monitoring program.     

Effect of Harvest on a Brown Bear Population in Alaska

There is a long and contentious history of brown bear (Ursus arctos) harvest management in Alaska, USA, the state that hosts the largest brown bear population in North America. In the mid-1990s, the Alaska Board of Game set the population objective for brown bears in Game Management Unit 13 A, located in interior southcentral Alaska, to be reduced by 50% to improve survival of moose (Alces alces) calves. The Board began further liberalizing brown bear harvest regulations for the unit beginning in regulatory year 1995, though adult females and their dependent offspring (i.e., cubs <2 yrs old) were protected. To evaluate progress toward this abundance objective, we captured and collared bears between 2006 and 2011 and conducted a capture-mark-resight density survey during summer 2011 for comparison to a similar baseline survey conducted in 1998. We report the results of the density survey and vital rates estimated from resight histories of collared bears and harvest information spanning from 1985 (10 years before establishment of the population objective) to 2012. There was a 25–40% reduction in abundance between 1998 and 2011. Population growth rates derived from density estimates and a matrix population projection model indicated that the population declined by 2.3–4.2% annually. We estimated harvest rates to be 8–15% annually, but harvest composition data indicated no changes in skull size, age distribution, or overall sex ratio. There was evidence of an increase in the proportion of older females in the harvest. Demographic analysis indicated high reproductive output and recruitment, potentially indicating a density-dependent compensatory response to reduced population size. Despite 13 years of harvest rates in excess of what had previously been considered to be sustainable for this population, the objective of reducing bear abundance by 50% had not been achieved as of 2011. The protection of females and dependent offspring in our study population appears to be a sufficient safeguard against a precipitous population decline while still permitting progress toward the population objective through high harvest on other segments of the population. © 2020 The Wildlife Society.     

Population and Harvest Dynamics of Midcontinent Sandhill Cranes

Sandhill cranes (Antigone canadensis) inhabiting the midcontinent of North America have been hunted since the 1960s under management goals of maintaining abundance, retaining geographic distribution, and maximizing sustainable harvest. Some biologists have raised concerns regarding harvest sustainability because sandhill cranes have lower reproductive rates than other game birds. We summarized demographic information in an age-structured matrix model to better understand population dynamics and harvest. Population indices and recovered harvest since the early 1980s suggest midcontinent sandhill cranes have experienced an average long-term annual growth of 0.9%; meanwhile, harvest has increased 1.8% annually. Adult survival and recruitment rates estimated from field data required modest adjustments (1–3%) so that model-derived growth rates matched growth estimated from a long-term survey (0.887 adult survival and 0.199 females/breeding female). Considering 0.9% long-term annual growth, sandhill cranes could be harvested at a rate of 6.6% if harvest was additive to natural mortality (assumed to be 0.05) or 11.3% if harvest mortality compensated for natural mortality. Life-history characteristics for long-lived organisms and demographic evidence suggested that hunter harvest was primarily additive. Differential harvest rates of segments of sandhill cranes in the midcontinent population derived from differential exposure to hunting suggested potentially unsustainable harvest for greater sandhill cranes (A. c. tabida) from 2 breeding segments. Overall, demographic evidence suggests that the harvest of sandhill cranes in the midcontinent population has been managed sustainably. Monitoring activities that reduce nuisance variation and estimate vital and harvest rates by subspecies would support continued management of sandhill cranes that are of interest to hunters and bird watchers. Published 2020. This article is a U.S. Government work and is in the public domain in the USA.     

Clustering Timber Harvests and the Effect of Dynamic Forest Management Policy on Forest Fragmentation

To integrate multiple uses (mature forest and commodity production) better on forested lands, timber management strategies that cluster harvests have been proposed. One such approach clusters harvest activity in space and time, and rotates timber production zones across the landscape with a long temporal period (dynamic zoning). Dynamic zoning has been shown to increase timber production and reduce forest fragmentation by segregating uses in time without reducing the spatial extent of timber production. It is reasonable to wonder what the effect of periodic interruptions in the implementation of such as strategy might be, as would be expected in a dynamic political environment. To answer these questions, I used a timber harvest simulation model (HARVEST) to simulate a dynamic zoning harvest strategy that was periodically interrupted by changes in the spatial dispersion of harvests, by changes in timber production levels, or both. The temporal scale (period) of these interruptions had impacts related to the rate at which the forest achieved canopy closure after harvest. Spatial dynamics in harvest policies had a greater effect on the amount of forest interior and edge than did dynamics in harvest intensity. The periodically clustered scenarios always produced greater amounts of forest interior and less forest edge than did their never clustered counterparts. The results suggest that clustering of harvests produces less forest fragmentation than dispersed cutting alternatives, even in the face of a dynamic policy future. Although periodic episodes of dispersed cutting increased fragmentation, average and maximum fragmentation measures were less than if clustered harvest strategies were never implemented. Clustering may also be useful to mitigate the fragmentation effects of socially mandated increases in timber harvest levels. Implementation of spatial clustering during periods of high timber harvest rates reduced the variation in forest interior and edge through time, providing a more stable supply of forest interior habitat across the landscape. Received 19 September 1997; accepted 6 August 1998.     

Factors contributing to carbon fluxes from bioenergy harvests in the U.S. Northeast: an analysis using field data

With growing interest in wood bioenergy there is uncertainty over greenhouse gas emissions associated with offsetting fossil fuels. Although quantifying postharvest carbon (C) fluxes will require accurate data, relatively few studies have evaluated these using field data from actual bioenergy harvests. We assessed C reductions and net fluxes immediately postharvest from whole‐tree harvests (WTH), bioenergy harvests without WTH, and nonbioenergy harvests at 35 sites across the northeastern United States. We compared the aboveground forest C in harvested with paired unharvested sites, and analyzed the C transferred to wood products and C emissions from energy generation from harvested sites, including indirect emissions from harvesting, transporting, and processing. All harvests reduced live tree C; however, only bioenergy harvests using WTH significantly reduced C stored in snags (P < 0.01). On average, WTH sites also decreased downed coarse woody debris C while the other harvest types showed increases, although these results were not statistically significant. Bioenergy harvests using WTH generated fewer wood products and resulted in more emissions released from bioenergy than the other two types of harvests, which resulted in a greater net flux of C (P < 0.01). A Classification and Regression Tree analysis determined that it was not the type of harvest or amount of bioenergy generated, but rather the type of skidding machinery and specifics of silvicultural treatment that had the largest impact on net C flux. Although additional research is needed to determine the impact of bioenergy harvesting over multiple rotations and at landscape scales, we conclude that operational factors often associated with WTH may result in an overall intensification of C fluxes. The intensification of bioenergy harvests, and subsequent C emissions, that result from these operational factors could be reduced if operators select smaller equipment and leave a portion of tree tops on site.     

An Evaluation of Sex-Age-Kill (SAK) Model Performance

ABSTRACT The sex-age-kill (SAK) model is widely used to estimate abundance of harvested large mammals, including white-tailed deer (Odocoileus virginianus). Despite a long history of use, few formal evaluations of SAK performance exist. We investigated how violations of the stable age distribution and stationary population assumption, changes to male or female harvest, stochastic effects (i.e., random fluctuations in recruitment and survival), and sampling efforts influenced SAK estimation. When the simulated population had a stable age distribution and λ > 1, the SAK model underestimated abundance. Conversely, when λ < 1, the SAK overestimated abundance. When changes to male harvest were introduced, SAK estimates were opposite the true population trend. In contrast, SAK estimates were robust to changes in female harvest rates. Stochastic effects caused SAK estimates to fluctuate about their equilibrium abundance, but the effect dampened as the size of the surveyed population increased. When we considered both stochastic effects and sampling error at a deer management unit scale the resultant abundance estimates were within ±121.9% of the true population level 95% of the time. These combined results demonstrate extreme sensitivity to model violations and scale of analysis. Without changes to model formulation, the SAK model will be biased when λ ≠ 1. Furthermore, any factor that alters the male harvest rate, such as changes to regulations or changes in hunter attitudes, will bias population estimates. Sex-age-kill estimates may be precise at large spatial scales, such as the state level, but less so at the individual management unit level. Alternative models, such as statistical age-at-harvest models, which require similar data types, might allow for more robust, broad-scale demographic assessments.     

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.     

Managing for Elevated Yield of Moose in Interior Alaska

ABSTRACT Given recent actions to increase sustained yield of moose (Alces alces) in Alaska, USA, we examined factors affecting yield and moose demographics and discussed related management. Prior studies concluded that yield and density of moose remain low in much of Interior Alaska and Yukon, Canada, despite high moose reproductive rates, because of predation from lightly harvested grizzly (Ursus arctos) and black bear (U. americanus) and wolf (Canis lupus) populations. Our study area, Game Management Unit (GMU) 20A, was also in Interior Alaska, but we describe elevated yield and density of moose. Prior to our study, a wolf control program (1976–1982) helped reverse a decline in the moose population. Subsequent to 1975, moose numbers continued a 28-year, 7-fold increase through the initial 8 years of our study (λ_B1 = 1.05 during 1996–2004, peak density = 1,299 moose/1,000 km²). During these initial 8 hunting seasons, reported harvest was composed primarily of males ( = 88%). Total harvest averaged 5% of the prehunt population and 57 moose/1,000 km², the highest sustained harvest-density recorded in Interior Alaska for similar-sized areas. In contrast, sustained total harvests of <10 moose/1,000 km² existed among low-density, predator-limited moose populations in Interior Alaska (≤417 moose/1,000 km²). During the final 3 years of our study (2004–2006), moose numbers declined (λ_B2 = 0.96) as intended using liberal harvests of female and male moose ( = 47%) that averaged 7% of the prehunt population and 97 moose/1,000 km². We intentionally reduced high densities in the central half of GMU 20A (up to 1,741 moose/1,000 km² in Nov) because moose were reproducing at the lowest rate measured among wild, noninsular North American populations. Calf survival was uniquely high in GMU 20A compared with 7 similar radiocollaring studies in Alaska and Yukon. Low predation was the proximate factor that allowed moose in GMU 20A to increase in density and sustain elevated yields. Bears killed only 9% of the modeled postcalving moose population annually in GMU 20A during 1996–2004, in contrast to 18–27% in 3 studies of low-density moose populations. Thus, outside GMU 20A, higher bear predation rates can create challenges for those desiring rapid increases in sustained yield of moose. Wolves killed 8–15% of the 4 postcalving moose populations annually (10% in GMU 20A), hunters killed 2–6%, and other factors killed 1–6%. Annually during the increase phase in GMU 20A, calf moose constituted 75% of the predator-killed moose and predators killed 4 times more moose than hunters killed. Wolf predation on calves remained largely additive at the high moose densities studied in GMU 20A. Sustainable harvest-densities of moose can be increased several-fold in most areas of Interior Alaska where moose density and moose: predator ratios are lower than in GMU 20A and nutritional status is higher. Steps include 1) reducing predation sufficient to allow the moose population to grow, and 2) initiating harvest of female moose to halt population growth and maximize harvest after density-dependent moose nutritional indices reach or approach the thresholds we previously published.     

The Sustainability of Wolverine Trapping Mortality in Southern Canada

Range declines, habitat connectivity, and trapping have created conservation concern for wolverines throughout their range in North America. Previous researchers used population models and observed estimates of survival and reproduction to infer that current trapping rates limit population growth, except perhaps in the far north where trapping rates are lower. Assessing the sustainability of trapping requires demographic and abundance data that are expensive to acquire and are therefore usually only achievable for small populations, which makes generalization risky. We surveyed wolverines over a large area of southern British Columbia and Alberta, Canada, used spatial capture-recapture models to estimate density, and calculated trapping kill rates using provincial fur harvest data. Wolverine density averaged 2 wolverines/1,000 km² and was positively related to spring snow cover and negatively related to road density. Observed annual trapping mortality was >8.4%/year. This level of mortality is unlikely to be sustainable except in rare cases where movement rates are high among sub-populations and sizable un-trapped refuges exist. Our results suggest wolverine trapping is not sustainable because our study area was fragmented by human and natural barriers and few large refuges existed. We recommend future wolverine trapping mortality be reduced by ≥50% throughout southern British Columbia and Alberta to promote population recovery. © 2019 The Authors. The Journal of Wildlife Management published by Wiley Periodicals, Inc. on behalf of The Wildlife Society.