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Despite decades of field research on greater sage-grouse, range-wide demographic data have yet to be synthesized into a sensitivity analysis to guide management actions. We reviewed range-wide demographic rates for greater sage-grouse from 1938 to 2011 and used data from 50 studies to parameterize a 2-stage, female-based population matrix model. We conducted life-stage simulation analyses to determine the proportion of variation in population growth rate (λ) accounted for by each vital rate, and we calculated analytical sensitivity, elasticity, and variance-stabilized sensitivity to identify the contribution of each vital rate to λ. As expected for an upland game bird, greater sage-grouse showed marked annual and geographic variation in several vital rates. Three rates were demonstrably important for population growth: female survival, chick survival, and nest success. Female survival and chick survival, in that order, had the most influence on λ per unit change in vital rates. However, nest success explained more of the variation in λ than did the survival rates. In lieu of quantitative data on specific mortality factors driving local populations, we recommend that management efforts for greater sage-grouse first focus on increasing female survival by restoring large, intact sagebrush-steppe landscapes, reducing persistent sources of human-caused mortality, and eliminating anthropogenic habitat features that subsidize species that prey on juvenile, yearling, and adult females. Our analysis also supports efforts to increase chick survival and nest success by eliminating anthropogenic habitat features that subsidize chick and nest predators, and by managing shrub, forb, and grass cover, height, and composition to meet local brood-rearing and nesting habitat guidelines. We caution that habitat management to increase chick survival and nest success should not reduce the cover or height of sagebrush below that required for female survival in other seasons (e.g., fall, winter). The success or failure of management actions for sage-grouse should be assessed by measuring changes in vital rates over long time periods to avoid confounding with natural, annual variation.

Recent declines in eastern wild turkeys (Meleagris gallopavo silvestris) have prompted increased interest in management and research of this important game species. However, the mechanisms underlying these declines are unclear, leaving uncertainty in how best to manage this species. Foundational to effective management of wildlife species is understanding the biotic and abiotic factors that influence demographic parameters and the contribution of vital rates to population growth. Our objectives for this study were to (1) conduct a literature review to collect all published vital rates for eastern wild turkey over the last 50 years, (2) perform a scoping review of the biotic and abiotic factors that have been studied relative to wild turkey vital rates and highlight areas that require additional research, and (3) use the published vital rates to populate a life‐stage simulation analysis (LSA) and identify the vital rates that make the greatest contribution to population growth. Based on published vital rates for eastern wild turkey, we estimated a mean asymptotic population growth rate (λ) of 0.91 (95% CI = 0.71, 1.12). Vital rates associated with after‐second‐year (ASY) females were most influential in determining population growth. Survival of ASY females had the greatest elasticity (0.53), while reproduction of ASY females had lower elasticity (0.21), but high process variance, causing it to explain a greater proportion of variance in λ. Our scoping review found that most research has focused on the effects of habitat characteristics at nest sites and the direct effects of harvest on adult survival, while research on topics such as disease, weather, predators, or anthropogenic activity on vital rates has received less attention. We recommend that future research take a more mechanistic approach to understanding variation in wild turkey vital rates as this will assist managers in determining the most appropriate management approach. Using a life‐stage simulation analysis, we show survival and reproduction of adult female wild turkeys had the greatest influence on population trajectories for this species. However, these life stages showed differing patterns in elasticity and variability, with adult survival having high elasticity but low process variance, and reproduction having lower elasticities but greater process variance. Additionally, we highlight several critical knowledge gaps regarding vital rates for different life stages and in the factors regulating or limiting wild turkeys.

To successfully respond to changing habitat, climate or harvest, managers need to identify the most effective strategies to reverse population trends of declining species and/or manage harvest of game species. A classic approach in conservation biology for the last two decades has been the use of matrix population models to determine the most important vital rates affecting population growth rate (λ), that is, sensitivity. Ecologists quickly realized the critical role of environmental variability in vital rates affecting λ by developing approaches such as life-stage simulation analysis (LSA) that account for both sensitivity and variability of a vital rate. These LSA methods used matrix-population modeling and Monte Carlo simulation methods, but faced challenges in integrating data from different sources, disentangling process and sampling variation, and in their flexibility. Here, we developed a Bayesian integrated population model (IPM) for two populations of a large herbivore, elk (Cervus canadensis) in Montana, USA. We then extended the IPM to evaluate sensitivity in a Bayesian framework. We integrated known-fate survival data from radio-marked adults and juveniles, fecundity data, and population counts in a hierarchical population model that explicitly accounted for process and sampling variance. Next, we tested the prevailing paradigm in large herbivore population ecology that juvenile survival of neonates <90 d old drives λ using our Bayesian LSA approach. In contrast to the prevailing paradigm in large herbivore ecology, we found that adult female survival explained more of the variation in λ than elk calf survival, and that summer and winter elk calf survival periods were nearly equivalent in importance for λ. Our Bayesian IPM improved precision of our vital rate estimates and highlighted discrepancies between count and vital rate data that could refine population monitoring, demonstrating that combining sensitivity analysis with population modeling in a Bayesian framework can provide multiple advantages. Our Bayesian LSA framework will provide a useful approach to addressing conservation challenges across a variety of species and data types.

We investigated survival, reproduction, and population growth (λ) for a declining elk (Cervus canadensis nelsoni) population in South Dakota, USA, 2011–2015. We obtained survival data from 125 calves and 34 yearlings. We determined survival and pregnancy rates for 42 adults (2–8 years old) and 39 old adults (≥8 years old). We combined population vital rates into a matrix model, which indicated a slightly growing population but with considerable uncertainty (λ̄ = 1.03, 95% CI = 0.93–1.13). Our elasticity analysis suggested asymptotic growth rates were most sensitive to proportional changes in old adult and adult female survival, followed by proportional changes in calf and yearling survival. Our life-stage simulation analysis further supported asymptotic growth rates being most sensitive to variation in survival, and most of the variation in λ we observed was a consequence of variation in annual calf survival (R² = 0.58). Annual calf survival was low (0.26, 95% CI = 0.05–0.52), and puma (Puma concolor) predation was the primary cause-specific mortality factor of calves (0.63, 95% CI = 0.51–0.76). Adult female survival was near its biological maximum (0.95, 95% CI = 0.87–0.99); therefore, managing for increased calf survival may be the most practical strategy for promoting elk population growth in this system. Managing this puma population at the lower end of the population objective and reducing white-tailed deer (Odocoileous virginianus) numbers (primary prey source) may allow for elk population growth in this system.

The wood duck (Aix sponsa) is a common and important cavity-nesting duck in North America; however, we know very little about how changes in vital rates influence population growth rate (λ). We used estimates of fertility and survival of female wood ducks from our nest-box studies in South Carolina, Alabama, and Georgia, USA, to create a stage-based matrix population model. We conducted perturbation analyses and ranked elasticity values to examine the relative importance of 17 component vital rates to λ. Female survival is influenced by nest success, so we recognized this female heterogeneity in our analyses. Four vital rates showed the greatest importance to λ. Analytic elasticities were greatest for breeding season and nonbreeding season survival of females that nested successfully, followed by nest success and female recruitment to the breeding population. Differences in female quality were important to λ. Next, we used process variation of vital rates and conducted life-stage simulation analyses (LSA) followed by variance decomposition to determine the amount of variation in λ explained by each vital rate. Female recruitment to the breeding population explained 57.7% of the variation in λ followed by nest success (11.4%), and breeding and nonbreeding season survival of females that nested successfully (9.3% and 9.4%, respectively). Together these 4 vital rates explained 88% of the variation in λ. Mean asymptotic population growth rate (λ = 0.80 ± 0.08 [SD]) from LSA revealed a declining population. Recruitment of females hatched from nest boxes was insufficient to sustain the nest-box population. However, including yearling (SY) females that were produced outside of nest boxes (i.e., immigrants) increased recruitment rates 1.5 to 2 times more than when only SY females recruited from nest boxes were included. Future research that examines how emigration and immigration interact with survival and reproduction to influence local population dynamics of wood ducks will be important for identifying the value of nest-box programs to wood duck conservation and management.

Mountain lions (Puma concolor) are widely hunted for recreation, population control, and to reduce conflict with humans, but much is still unknown regarding the effects of harvest on mountain lion population dynamics. Whether human hunting mortality on mountain lions is additive or compensatory is debated. Our primary objective was to investigate population effects of harvest on mountain lions. We addressed this objective with a management experiment of 3 years of intensive harvest followed by a 6-year recovery period. In December 2000, after 3 years of hunting, approximately 66% of a single game management unit within the Blackfoot River watershed in Montana was closed to lion hunting, effectively creating a refuge representing approximately 12% (915 km²) of the total study area (7,908 km²). Hunting continued in the remainder of the study area, but harvest levels declined from approximately 9/1,000 km² in 2001 to 2/1,000 km² in 2006 as a result of the protected area and reduced quotas outside. We radiocollared 117 mountain lions from 1998 to 2006. We recorded known fates for 63 animals, and right-censored the remainder. Although hunting directly reduced survival, parameters such as litter size, birth interval, maternity, age at dispersal, and age of first reproduction were not significantly affected. Sensitivity analysis showed that female survival and maternity were most influential on population growth. Life-stage simulation analysis (LSA) demonstrated the effect of hunting on the population dynamics of mountain lions. In our non-hunted population, reproduction (kitten survival and maternity) accounted for approximately 62% of the variation in growth rate, whereas adult female survival accounted for 30%. Hunting reversed this, increasing the reliance of population growth on adult female survival (45% of the variation in population growth), and away from reproduction (12%). Our research showed that harvest at the levels implemented in this study did not affect population productivity (i.e., maternity), but had an additive effect on mountain lion mortality, and therefore population growth. Through harvest, wildlife managers have the ability to control mountain lion populations.

The realized impact of a vital rate on population growth (λ) is determined by both the relative influence of the vital rate on λ (elasticity) and its magnitude of variability. We estimated mean survival and reproductive rates in elk (Cervus elaphus) and spatial and temporal variation in these rates from 37 sources located primarily across the Rocky Mountain region and northwestern United States. We removed sampling variance from estimates of process variance both within and across vital-rate data sets using the variance discounting method developed by White (2000). Deterministic elasticities calculated from a population matrix model parameterized with these mean vital rates ranked adult female survival (eScow = 0.869) much higher than calf survival (eScalf = 0.131). However, process variance in calf survival (σ̂2Scalf = 0.039) was >11 times greater than process variance in female survival (σ̂2Scow = 0.003) across data sets and 10 times greater on average (2Scalf = 0.020; 2Scow = 0.002) within studies. We conducted Life-Stage Simulation Analysis to incorporate both vital-rate elasticity patterns and empirical estimates of variability to identify those vital rates most influential in elk population dynamics. The overwhelming magnitude of variation in calf survival explained 75% of the variation in the population growth rates generated from 1,000 matrix replicates, compared to just 16% of the variation in λ explained by variation in female survival. Variation in calf survival greatly impacts elk population growth and calls into question the utility of classical elasticity analysis alone for guiding elk management. These results also suggest that the majority of interannual variability that wildlife managers document in late-winter and spring elk surveys is attributable to variation in calf survival over the previous year and less influenced by variation in the harvest of females during the preceding autumn. To meet elk population size objectives, managers should consider the inherent variation in calf survival, and its apparent sensitivity to management, in addition to female harvest.

The northern bobwhite (Colinus virginianus) is an economically important gamebird that is currently undergoing widespread population declines. Despite considerable research on the population ecology of bobwhites, there have been few attempts to model population dynamics of bobwhites to determine the contributions of different demographic parameters to variance of the finite rate of population change (λ). We conducted a literature review and compiled 405 estimates of 9 demographic parameters from 49 field studies of bobwhites. To identify demographic parameters that might be important for management, we used life-stage simulation analyses (LSA) to examine sensitivity of λ to simulated variation in 9 demographic parameters for female bobwhites. In a baseline LSA based on uniform distributions bounded by the range of estimates for each demographic parameter, bobwhite populations were predicted to decline (λ = 0.56) and winter survival of adults made the greatest contribution to variance of λ (r2 = 0.453), followed by summer survival of adults (r2 = 0.163), and survival of chicks (r2 = 0.120). Population change was not sensitive to total clutch laid, nest survival, egg hatchability, or 3 parameters associated with the number of nesting attempts (r2 <0.06). Our conclusions were robust to alternative simulation scenarios, and parameter rankings changed only if we adjusted the lower bounds of winter survival upwards. Bobwhite populations were not viable with survival rates reported from most field studies. Survival rates may be depressed below sustainable levels by environmental conditions or possibly by impacts of capture and telemetry methods. Overall, our simulation results indicate that management practices that improve seasonal survival rates will have the greatest potential benefit for recovery of declining populations of bobwhites.

Age ratios (e.g., calf:cow for elk and fawn:doe for deer) are used regularly to monitor ungulate populations. However, it remains unclear what inferences are appropriate from this index because multiple vital rate changes can influence the observed ratio. We used modeling based on elk (Cervus elaphus) life-history to evaluate both how age ratios are influenced by stage-specific fecundity and survival and how well age ratios track population dynamics. Although all vital rates have the potential to influence calf:adult female ratios (i.e., calf:cow ratios), calf survival explained the vast majority of variation in calf:adult female ratios due to its temporal variation compared to other vital rates. Calf:adult female ratios were positively correlated with population growth rate (λ) and often successfully indicated population trajectories. However, calf:adult female ratios performed poorly at detecting imposed declines in calf survival, suggesting that only the most severe declines would be rapidly detected. Our analyses clarify that managers can use accurate, unbiased age ratios to monitor arguably the most important components contributing to sustainable ungulate populations, survival rate of young and λ. However, age ratios are not useful for detecting gradual declines in survival of young or making inferences about fecundity or adult survival in ungulate populations. Therefore, age ratios coupled with independent estimates of population growth or population size are necessary to monitor ungulate population demography and dynamics closely through time.

Demographic studies of imperiled populations can aid managers in planning conservation actions. However, applicability of findings for a single population across a species’ range is sometimes questionable. We conducted long-term studies (8 and 9 years, respectively) of 2 populations of the lizard Phrynosoma cornutum separated by 1000 km within the historical distribution of the species. The sites were a 15-ha urban wildlife reserve on Tinker Air Force Base (TAFB) in central Oklahoma and a 6000-ha wildland site in southern Texas, the Chaparral Wildlife Management Area (CWMA). We predicted a trade-off between the effect of adult survival and fecundity on population growth rate (λ), leading to population-specific contributions of individual vital rates to λ and individualized strategies for conservation and management of this taxon. The CWMA population had lower adult survival and higher fecundity than TAFB. As predicted, there was a trade-off in the effects of adult survival and fecundity on λ between the two sites; fecundity affected λ more at CWMA than at TAFB. However, adult survival had the smallest effect on λ in both populations. We found that recruitment in P. cornutum most affected λ at both sites, with hatchling survival having the strongest influence on λ. Management strategies focusing on hatchling survival would strongly benefit both populations. As a consequence, within the constraint of the need to more accurately estimate hatchling survival, managers across the range of species such as P. cornutum could adopt similar management priorities with respect to stage classes, despite intra-population differences in population vital rates.