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USGS2021

Brown treesnake mortality after aerial application of toxic baits

Quantitative evaluation of control tools for managing invasive species is necessary to assess overall effectiveness and individual variation in treatment susceptibility. Invasive brown treesnakes ( Boiga irregularis ) on Guam have caused severe ecological and economic effects, pose a risk of accidental introduction to other islands, and are the greatest impediment to the reestablishment of extirpated native fauna. An aerial delivery system for rodent-based toxic baits can reduce brown treesnake abundance and heterogeneity among individuals may influence bait attraction or toxicant susceptibility. Previous baiting trials have either been simulated aerial treatments or relied on slightly different bait capsule compositions and the results of aerial delivery of toxic baits under operational conditions may not be directly comparable. We monitored 30 radio-tagged adult snakes (990–1,265 mm snout-vent length) during an aerial baiting operation in a 55-ha area using transmitters equipped with accelerometers and receivers programed to display a status code indicating mortality if a snake failed to move for >24 hours. We used known-fate models to estimate mortality and evaluate a priori hypotheses explaining differences in mortality based on size, sex, and treatment effects. Eleven radio-tagged snakes died in the aerial baiting treatment period (0.37, 95% CI = 0.21–0.55) and no individuals (0.00, 95% CI = 0.00–0.04) died during the non-treatment period. Our data provide strong evidence for an additive size-based treatment effect on mortality, with smaller adults (0.59, 95% CI = 0.35–0.80) exhibiting higher mortality than larger snakes (0.14, 95% CI = 0.02–0.37) but did not support a sex effect on mortality. The high mortality of snakes during the treatment period indicates that aerial baiting can reduce brown treesnake abundance, but further refinement or use in combination with other removal tools may be necessary to overcome size-based differences in susceptibility and achieve eradication.

Journal of Wildlife Management↗

USGS2019

Trends and carrying capacity of sea otters in Southeast Alaska

Sea otter populations in Southeast Alaska (SEAK) have increased dramatically from fewer than 500 translocated animals in the late 1960s. The recovery of sea otters to ecosystems from which they had been absent has affected coastal food webs, including commercially important fisheries, and thus information on expected growth and equilibrium abundances can help inform resource management. We compile available survey data for SEAK and fit a Bayesian state-space model to estimate past trends and current abundance. Our model improves upon previous analyses by partitioning and quantifying sources of estimation error, accounting for over-dispersion of aerial count data, and providing realistic measurements of uncertainty around point estimates of abundance at multiple spatial scales. We also provide the first estimates of carrying capacity (K) for SEAK, at both regional and sub-regional scales, and analyze growth rates, current population status and expected future trends. At the regional scale, the population increased from 13,221 otters in 2003 (95% credible interval 9,990 – 16,828) to 25,584 otters in 2011 (CI95 18,739 – 33,163). The average annual growth rate in southern SEAK (7.8%) was higher than northern SEAK (2.7%); however, growth varied at the sub-regional scale and there was a negative relationship between growth rates and the number of years sea otters were present in an area. Local populations vary in terms of current densities and expected future growth: the mean estimated density at K was 4.2 (1.58) sea otters per km2 of habitat (defined as the sub-tidal benthos between 0-40m depth) and current densities correspond on average to 50% of projected equilibrium values (range = 1% to 97%) with the earliest-colonized sub-regions tending to be closer to K. Assuming a similar range of equilibrium densities for currently un-occupied habitats in SEAK, the projected value of K for all of SEAK is 74,650 sea otters (CI95 =36,778–136,506). Future analyses can improve upon the precision of K estimates by employing more frequent surveys at index sites and incorporating environmental covariates into the process model to generate habitat-specific estimates of equilibrium density.

Alaska↗

USGS2021

Experimental evaluation of predator exclosures on nest, chick, and adult survival of piping plovers

Species of conservation concern often receive intensive management to improve vital rates and facilitate recovery. Piping plovers ( Charadrius melodus ) are federally listed in the United States and concerns over nest depredation have prompted widespread use of plover-permeable predator exclosures placed around nests (0.5–2-m radius). While effectiveness of exclosures for improving nest survival has been demonstrated, concerns remain about decreased chick survival (through predator cueing or density-dependent processes) or increased vulnerability of adults to predation (ambush as adult leaves exclosure). Either one of these concerns could demographically outweigh the benefits of increased nest survival. During 2014–2016, we conducted an experiment designed to evaluate survival of uniquely identified nests ( n = 418), chicks ( n = 453), and adults ( n = 367) at wetlands across the Northern Great Plains, USA. We assigned wetlands ( n 2014 = 26, n 2015 = 28, n 2016 = 25) into 2 groups: wetlands in which half of the nests received exclosures and wetlands in which none of the nests received exclosures. Exclosed nests had greater cumulative survival (0.73 [85% CI = 0.70–0.77]) than unexclosed nests at treatment wetlands (0.58 [0.54–0.62]) or unexclosed nests at control wetlands (0.52 [0.49–0.56]). Survival to fledging was highest for chicks hatched from exclosed nests (0.51 [0.47–0.56]), and similar between chicks hatched from unexclosed nests at treatment (0.34 [0.30–0.39]) and control (0.37 [0.32–0.42]) wetlands. Cumulative survival of adults during incubation varied by exclosure status, but adults associated with exclosed nests (0.90 [0.88–0.93]) and unexclosed nests at treatment wetlands (0.89 [0.86–0.92]) had greater survival than those associated with unexclosed nests at control wetlands (0.75 [0.64–0.84]). Adult annual survival rates varied by year (0.79–0.95) but not by exclosure status. The positive influence of exclosures on nest survival was not offset by a reduction in chick or adult survival, indicating that exclosures are a viable tool for piping plover conservation.

Montana, North Dakota↗

USGS2021

Using fecal DNA and closed-capture models to estimate feral horse population size

Accurate population estimates provide the foundation for managing feral horses ( Equus caballus ferus ) across the western United States. Certain feral horse populations are protected by the Wild and Free-Roaming Horses and Burros Act of 1971 and managed by the Bureau of Land Management (BLM) or the United States Forest Service on designated herd management areas (HMAs) or wild horse territories, respectively. Horses are managed to achieve an appropriate management level (AML), which represents the number of horses determined by BLM to contribute to a thriving natural ecological balance and avoid deterioration of the range. To achieve AML for each HMA, BLM resource managers need accurate and precise population estimates. We tested the use of non-invasive fecal samples in a genetic capture-recapture framework to estimate population size in a closed horse population at the Little Book Cliffs HMA, Colorado, USA, with a known size of 153 individuals. We collected 1,957 samples over 3 independent sampling periods in 2014 and amplified them at 8 microsatellite loci. We applied mark-recapture models to determine population size using 954 samples that amplified at all 8 loci. We subsampled and reanalyzed our dataset to simulate different data collection protocols and evaluated effects on accuracy and precision of estimates using N-mixture modeling, full likelihood closed-capture modeling, and capwire single-occasion modeling that used data from all 3 sampling periods. Our model results were accurate and precise for analyses that used data from all 3 occasions; however, capwire single-occasion modeling was not accurate when we analyzed each sampling period separately. For all subsampling analysis scenarios, reducing sample size decreased precision, whether by reducing number of field staff, field days, or geographic areas surveyed on each period. Reducing spatial coverage of the survey area did not result in accurate population estimates and only marginally lowered the number of samples that would need to be collected to maintain accuracy. Because laboratory analysis contributes the greatest expense for this method ($80 U.S./sample), reducing fecal sample size is advantageous. Our results demonstrate that non-invasive sampling combined with good survey design and careful genetic and capture-recapture analyses can provide an alternative method to estimate the number of feral horses in a closed population. This method may be especially appropriate in situations where aerial inventories are not practical or accurate because of low sighting conditions. But the higher costs associated with laboratory sample analyses may reduce the method's feasibility compared to helicopter surveys.

Colorado↗

USGS2015

An empirical evaluation of landscape energetic models: Mallard and American black duck space use during the non-breeding period

Bird conservation Joint Ventures are collaborative partnerships between public agencies and private organizations that facilitate habitat management to support waterfowl and other bird populations. A subset of Joint Ventures has developed energetic carrying capacity models (ECCs) to translate regional waterfowl population goals into habitat objectives during the non-breeding period. Energetic carrying capacity models consider food biomass, metabolism, and available habitat to estimate waterfowl carrying capacity within an area. To evaluate Joint Venture ECCs in the context of waterfowl space use, we monitored 33 female mallards ( Anas platyrhynchos ) and 55 female American black ducks ( A. rubripes ) using global positioning system satellite telemetry in the central and eastern United States. To quantify space use, we measured first-passage time (FPT: time required for an individual to transit across a circle of a given radius) at biologically relevant spatial scales for mallards (3.46 km) and American black ducks (2.30 km) during the non-breeding period, which included autumn migration, winter, and spring migration. We developed a series of models to predict FPT using Joint Venture ECCs and compared them to a biological null model that quantified habitat composition and a statistical null model, which included intercept and random terms. Energetic carrying capacity models predicted mallard space use more efficiently during autumn and spring migrations, but the statistical null was the top model for winter. For American black ducks, ECCs did not improve predictions of space use; the biological null was top ranked for winter and the statistical null was top ranked for spring migration. Thus, ECCs provided limited insight into predicting waterfowl space use during the non-breeding season. Refined estimates of spatial and temporal variation in food abundance, habitat conditions, and anthropogenic disturbance will likely improve ECCs and benefit conservation planners in linking non-breeding waterfowl habitat objectives with distribution and population parameters. Published 2015. This article is a U.S. Government work and is in the public domain in the USA.

Arkansas, Delaware, Louisiana, Michigan, New Jerse↗

USGS2016

Environmental factors influence lesser scaup migration chronology and population monitoring

Identifying environmental metrics specific to lesser scaup ( Aythya affinis ; scaup) spring migration chronology may help inform development of conservation, management and population monitoring. Our objective was to determine how environmental conditions influence spring migration of lesser scaup to assess the effectiveness of the Waterfowl Breeding Population and Habitat Survey in accurately estimating scaup populations. We first compared peak timing of mallard ( Anas platyrhynchos ) and scaup migration from weekly ground surveys in North Dakota, USA because the Waterfowl Breeding Population and Habitat Survey is designed to capture annual mallard migration. As predicted, we detected that peak timing of scaup and mallard migrations differed in 25 of 36 years investigated (1980–2010). We marked scaup with satellite transmitters ( n = 78; 7,403 locations) at Long Point, Lake Erie, Ontario, Canada; Pool 19 of the Mississippi River, Iowa and Illinois, USA; and Presque Isle Bay, Lake Erie, Pennsylvania, USA. We tested the assumption that our marked scaup were representative of the continental population using the traditional survey area by comparing timing of migration of marked birds and scaup counted in the North Dakota Game and Fish Department survey. We detected a strong positive correlation between marked scaup and the survey data, which indicated that marked scaup were representative of the population. We subsequently used our validated sample of marked scaup to investigate the effects of annual variation in temperature, precipitation, and ice cover on spring migration chronology in the traditional and eastern survey areas of the Waterfowl Breeding Population and Habitat Survey, 2005–2010. We evaluated competing environmental models to explain variation in timing and rate of scaup migration at large-scale and local levels. Spring migration of scaup occurred earlier and faster during springs with warmer temperatures and greater precipitation, variables known to influence energy budgets and wetland availability. Our results suggest that surveys designed to index abundance of breeding mallards is imprecise for estimating scaup abundance, and inaccurate at estimating breeding population size by survey stratum.

Journal of Wildlife Management↗

USGS2018

Incorporating detection probability to estimate pheasant density

ndices of abundance, such as point counts, commonly are used to monitor trends in bird populations. In some circumstances, however, an index of abundance provides insufficient information for making management decisions and accurate density estimates are necessary. Wild ring-necked pheasants ( Phasianus colchicus ) were translocated to 10 study areas in Pennsylvania from 2007 to 2014 with the goal of establishing female densities of 3.86 pheasants/km 2 . We developed a population density estimator that used 3-minute crowing counts adjusted for probability of detection to estimate male pheasant density and flushing surveys to estimate the female:male ratio. To account for detection probability, we estimated the probability a pheasant was available to be detected by monitoring crowing frequency of male pheasants fitted with radio-transmitters and the probability an observer was able to detect a crowing pheasant at distances from 0 to 0.93 km. We found the probability a pheasant crowed during 3 minutes decreased linearly over our survey period from 0.66 in mid-April to 0.46 by the end of May. At the farthest distance we were able to accurately detect a crowing pheasant. We estimated the probability of detecting a pheasant at 0.80 km to be 0.019 ± 0.005 (SE), which means that we could not assume any fixed distance beyond which crowing birds could not be detected. Therefore, we replaced the probability of detection in the standard distance sampling estimator with the effective area of detection. The estimation of the effective area of detection is robust to choice of radius of the point and did not require observers to estimate the distance to crowing pheasants. We estimated the female:male ratio to be 1.02:1, despite the ratio of released pheasants being 4.46:1. Only 1 study area achieved the female density goal ( = 4.16); the maximum density at all other study areas was <2 females/km 2 . The estimator we developed incorporated multiple detection probabilities to provide density estimates and simplified the crowing count protocol by eliminating the need for observers to estimate their distance from a detected bird, which makes the estimator useful for estimation of population abundance when explicit population density objectives must be evaluated.

Pennsylvania↗

USGS2005

Impact of special early harvest seasons on subarctic-nesting and temperate-nesting Canada geese

Dramatic changes in wintering distributions of Canada geese ( Branta canadensis ) have occurred over the past 50 years in eastern North America. Declines in numbers of subarctic-nesting geese wintering in southern states, and increases in numbers wintering in northern regions, have resulted in a northern shift in winter distributions. In contrast, numbers of temperate-nesting geese have increased throughout eastern North America. Management efforts to control overabundant temperate-nesting flocks have included the establishment of special early harvest seasons in September. However, the effect of early seasons on survival and harvest of subarctic-nesting populations has not been documented. Understanding the timing of migration movements and the fidelity of subarctic-nesting flocks to terminal winter refuges in the Southeast also is necessary to design early harvest seasons that target temperate-nesting flocks and protect subarctic-nesting populations. We used recoveries of marked geese to estimate survival and harvest rates before and after implementation of early harvest seasons within the Mississippi Flyway during 1976–1999. In addition, we used observations of neck-banded geese from the Southern James Bay Population (SJBP) to evaluate the hypothesis that subarctic-nesting geese arriving prior to mid-December on several key terminal winter refuges in the Southeast (early arriving migrants) were more likely to return to those refuges in subsequent years than were migrants arriving after mid-December (late arriving migrants). September seasons during 1987–1994 were a minor source of mortality for subarctic-nesting populations and accounted for <10% of their annual harvest mortality. The effectiveness of early seasons for increasing mortality of temperate-nesting flocks varied among the states we examined and was tempered by concurrent changes in state-specific harvest regulations during the regular harvest season. For SJBP Canada geese, annual fidelity to southeastern refuges was 10% higher for early arrivers than for late arriving geese. However, in any given year only 47–57% of the surviving geese were expected to return to the refuges the following year. Although early arriving migrants had higher survival and higher return probabilities than did late arriving migrants or geese that failed to return, numbers of geese wintering on southeastern refuges likely declined because <60% of the surviving geese affiliated with the refuges would return in a given year and because of lower survival for geese that did not return to the refuges.

Journal of Wildlife Management↗

USGS2021

Aural and visual detection of greater sage-grouse leks: Implications for population trend estimates

Counts of greater sage-grouse ( Centrocercus urophasianus ) at leks have been used in harvest management, Endangered Species Act listing decisions, and land management policies for over half a century. Lek count sampling methods focus on counting male sage-grouse at known leks, primarily those observed visually from roads or vantage points, but leks are likely missed that are unknown prior to the survey and are difficult to detect while driving between known lek sites. One way to ameliorate this shortfall may be to conduct short point-count surveys at multiple stops along lek-survey routes or while driving between lek counts, thereby detecting newly established or unknown leks. To evaluate the feasibility of this approach, we estimated aural and visual detection probability of active sage-grouse leks during 1-minute point-count surveys at known distances and examined the effects of environmental factors on aural lek detection in southern Idaho, USA, 2016–2017. Our results demonstrate that field observers can aurally detect sage-grouse leks at approximately 3 times greater distances compared to detecting leks visually. The probability of hearing an active lek was highest near the peak of male and female attendance (8 Apr), within an hour of sunrise, on relatively calm and cold days, when the observer was at a higher elevation relative to the lek, and during conditions with no background noise. Detection probability declined with distance and the probability of aural detection was 0.59 at 1 km from a lek when other variables were held at their means. Hence, conducting ≥3 1-minute surveys along a lek route would be expected to detect ≥93% of all leks within 1.5 km of each survey under the average environmental conditions in our study. Our results suggest that surveys could greatly improve detection of unknown or newly established leks and can facilitate a more accurate assessment of sage-grouse population trends through lek counts. Moreover, our results demonstrate how environmental factors influence the detection of leks during surveys, and therefore which variables should be considered for inclusion in any future revisions of lek count protocols or in analyses of lek count data.

Idaho↗

USGS2012

Estimating abundance of mountain lions from unstructured spatial sampling

Mountain lions (Puma concolor) are often difficult to monitor because of their low capture probabilities, extensive movements, and large territories. Methods for estimating the abundance of this species are needed to assess population status, determine harvest levels, evaluate the impacts of management actions on populations, and derive conservation and management strategies. Traditional mark–recapture methods do not explicitly account for differences in individual capture probabilities due to the spatial distribution of individuals in relation to survey effort (or trap locations). However, recent advances in the analysis of capture–recapture data have produced methods estimating abundance and density of animals from spatially explicit capture–recapture data that account for heterogeneity in capture probabilities due to the spatial organization of individuals and traps. We adapt recently developed spatial capture–recapture models to estimate density and abundance of mountain lions in western Montana. Volunteers and state agency personnel collected mountain lion DNA samples in portions of the Blackfoot drainage (7,908 km 2 ) in west-central Montana using 2 methods: snow back-tracking mountain lion tracks to collect hair samples and biopsy darting treed mountain lions to obtain tissue samples. Overall, we recorded 72 individual capture events, including captures both with and without tissue sample collection and hair samples resulting in the identification of 50 individual mountain lions (30 females, 19 males, and 1 unknown sex individual). We estimated lion densities from 8 models containing effects of distance, sex, and survey effort on detection probability. Our population density estimates ranged from a minimum of 3.7 mountain lions/100 km 2 (95% Cl 2.3–5.7) under the distance only model (including only an effect of distance on detection probability) to 6.7 (95% Cl 3.1–11.0) under the full model (including effects of distance, sex, survey effort, and distance x sex on detection probability). These numbers translate to a total estimate of 293 mountain lions (95% Cl 182–451) to 529 (95% Cl 245–870) within the Blackfoot drainage. Results from the distance model are similar to previous estimates of 3.6 mountain lions/100 km 2 for the study area; however, results from all other models indicated greater numbers of mountain lions. Our results indicate that unstructured spatial sampling combined with spatial capture–recapture analysis can be an effective method for estimating large carnivore densities.

Journal of Wildlife Management↗

USGS2023

Survival and establishment of captive-reared and translocated giant gartersnakes after release

Many imperiled species face increasing extinction risk that requires interventional management like translocation or captive rearing. The use of translocations to successfully restore or create populations requires that animals survive at recipient sites, information that is often lacking for imperiled species and that can be risky to acquire if not obtained before a species has dwindled in number. The giant gartersnake ( Thamnophis gigas ), a semiaquatic snake endemic to the Central Valley in California, USA, has declined after losing >90% of its historical habitat and may benefit from successful translocations to protected habitat. We released adult and captive-reared juvenile snakes from 2 donor sites into a recently restored wetland in 2019 and 2020 and compared their survival, movement, and activity using radio-telemetry through 2021. We monitored juvenile survival for 2 years in captivity after birth and then estimated post-release survival at the recipient site using radio-telemetry. Just 8% of translocated adult snakes survived >801 days (95% CI = 1–64%) compared with 39% of resident snakes at the donor sites surviving >1,154 days (95% CI = 23–68%). This equated to annualized survival rates of translocated adults ( x̄ = 0.32, 95% CI = 0.12–0.82) that were roughly half that of resident snakes ( x̄ = 0.74, 95% CI = 0.63–0.89). Translocation was negatively correlated with survival, but movement and activity received little support in models. Seventy-six percent of juvenile snakes survived captivity and, once released, juvenile survival was 60% (95% CI = 38–94%) for the 4-month monitoring period before winter. It is unclear why survival of translocated adult snakes was lower than that of resident snakes, but there was little evidence for differences in behavior (e.g., increased surface activity, average distance moved, emigration from the translocation site) that are commonly cited causes of mortality in other translocation studies. Our results suggest that, in the absence of a clear understanding as to what contributes to adult survival after release to a new site, future work using captive-rearing and juvenile translocation may be more promising for establishing and recovering populations than just translocating adults given the high survival of juveniles.

California↗

USGS2018

Lesser prairie-chicken space use among landscapes in relation to anthropogenic structures

The Southern Great Plains has been altered by conversion of native grassland to row‐crop agriculture, which is considered the primary cause of declining lesser prairie‐chicken ( Tympanuchus pallidicinctus ) populations. However, recent analyses indicate that direct loss of grassland has slowed while lesser prairie‐chicken populations continue to decline, suggesting that remaining grasslands potentially suffer from degradation by various land uses (e.g., increased anthropogenic disturbance). Understanding the spatial ecology of lesser prairie‐chickens relative to anthropogenic structures is important for conservation planning, habitat management, and infrastructure mitigation. We investigated effects of proximity to anthropogenic structures on home range and nest placement (second‐order selection) and within home range space use (third‐order selection) of radio‐marked lesser prairie‐chickens ( n = 285) at 2 scales of selection using resource utilization functions and resource selection functions. We collected data from birds marked in the Mixed‐Grass Prairie and Short‐Grass Prairie ecoregions of Kansas, USA, from 15 March 2013 to 14 March 2016. Home range placement did not vary by region or season, and lesser prairie‐chickens placed home ranges farther from powerlines and roads than would be expected at random. As distance increased from 0 to 3 km away from roads and powerlines, the relative probability of home range placement increased 1.66 and 1.54 times, respectively. Distance to powerline was the single most consistent variable negatively affecting nest placement. As the distance from powerline increased from 0 to 3 km, the relative probability of nest placement increased 2.19 times. Distance to oil well did not influence placement of home ranges or nests. When pooled across regions, lesser prairie‐chickens exhibited behavioral avoidance of powerlines, roads, and oil wells within their home range. Lesser prairie‐chickens, on average, used space at greater intensities within their home range farther from wells, powerlines, and roads than available. Across breeding season phases, we found no evidence of increased behavioral avoidance of anthropogenic structures during the nesting or brooding phases compared to the lekking or post‐breeding phases. Within home range space use during the brooding phase was not related to powerlines, wells, or roads. Our results indicate that avoidance of anthropogenic structures may result in functional habitat loss and continued fragmentation of remaining grassland habitat. Reduction or elimination of anthropogenic development in quality lesser prairie‐chicken habitat and concentrating new development in already altered areas that are avoided by lesser prairie‐chickens and no longer considered available habitat may reduce continued habitat degradation throughout the species’ range and aid in population persistence.

Journal of Wildlife Management↗

USGS2017

Declining survival of black brant from subarctic and arctic breeding areas

Since the mid 1990s, the number of black brant ( Branta bernicla nigricans ; brant) nests on the Yukon‐Kuskokwim Delta (YKD), Alaska, USA, the historically predominant breeding area of brant, has declined steadily. This has caused researchers and managers to question if arctic breeding populations can compensate for the reduction in brant nests on the YKD. An important component of the assessment of brant population dynamics is having current estimates of first‐year and adult survival. We banded brant at 4 locations in Arctic Alaska and western Canada, and at 1 location in the subarctic, the Tutakoke River (TR) colony on the YKD, 1990–2015. We used joint live and dead mark‐recapture models to estimate first‐year and adult (≥1 yr old) survival of brant. We also used band recovery rates from a Brownie model to assess temporal trends in band recovery rates of adult brant. First‐year survival of brant hatched at TR declined from approximately 0.60 to <0.20 and, although first‐year survival generally was higher for goslings marked in the Arctic, their survival declined from approximately 0.70 in the early 1990s to ≤0.45 in the 2010s. Annual survival of adult females decreased from an average of 0.881 (95% CI = 0.877–0.885) to 0.822 (95% CI = 0.815–0.829) at TR and from 0.851 (95% CI = 0.843–0.860) to 0.821 (95% CI = 0.805–0.836) in the Arctic, from 1990 to 2014. Band recovery rates of adults generally were <1.25% until the last several years of study, when they reached ≤3.5%. Although the current harvest rates may be partially additive to natural mortality, we do not believe that harvest is the main influence on the declines in survival. The general decline in survival rates of brant breeding across a large geographic area may be influenced by a reduction in the quality of migration and wintering ground habitats. We suggest an analysis of seasonal survival of brant to test the hypothesis that declining habitat quality on wintering or spring migration areas is reducing survival. Our results suggest that the number of breeding pairs at TR will continue to decline and also brings into question the ability of arctic breeding populations to grow at a rate necessary to offset the declines on the YKD. Researchers should continue to closely monitor survival and harvest rates of brant, and assess methods currently used to monitor their abundance.

Journal of Wildlife Management↗

USGS2023

Survival, cause-specific mortality, and population growth of white-tailed deer in western Virginia

Understanding the role of recruitment in population dynamics of white-tailed deer ( Odocoileus virginianus ) is important for management. In the central Appalachian Mountains, deer are part of a largely forested ecosystem that supports 3 carnivore species thought to be capable of influencing white-tailed deer recruitment: black bears ( Urus americanus ), coyotes ( Canis latrans ), and bobcats ( Lynx rufus ). Yet little is known about predation, how other environmental factors influence recruitment, or the importance of neonate survival to white-tailed deer population performance in the region. Our objectives were to identify causes of mortality for neonates, analyze effects of landscape attributes on survival of neonates, estimate survival rates for neonates and adult female white-tailed deer, and to model population growth trends based on current vital rates and hypothetical harvest and neonate survival scenarios. During 2019–2020, we captured 57 neonate deer in Bath County, Virginia, USA, by monitoring 38 pregnant females equipped with global positioning system collars and vaginal implant transmitters and by conducting transect searches for recently born neonates. We observed 37 neonate mortalities and identified cause of death using field and genetic evidence. Mortalities included 28 predation events and 9 deaths from other causes (e.g., abandonment, malnutrition, disease). Black bears accounted for 48.6% of neonate mortalities, and 64.2% of predation events ( n = 18), followed by bobcats ( n = 5) and coyotes ( n = 3). Annual survival for adult female deer was 0.871 and neonate survival to 12 weeks old was 0.310. Elevation was a significant predictor of neonate survival; mortality risk increased 20% for every 100-m increase in elevation. Models of annual population growth using observed vital rates predicted an increasing population (λ = 1.10). A 10% increase in female harvest would still result in a potential population increase of 2% (λ = 1.02), but a 20% increase in harvest rate would result in a potential 7% decline (λ = 0.93). Neonate survival was higher near fertile valley bottoms and lower along forested ridges characterized by shallow, infertile soils and limited edge or early successional forests. While predation, largely influenced by black bears, was the leading cause of neonate mortality and contributed to low neonate survival, we observed little evidence of population decline, and suggest there is opportunity for a modest increase in harvest of female deer.

Virginia↗

USGS2021

Habitat features predict carrying capacity of a recovering marine carnivore

The recovery of large carnivore species from over‐exploitation can have socioecological effects; thus, reliable estimates of potential abundance and distribution represent a valuable tool for developing management objectives and recovery criteria. For sea otters ( Enhydra lutris ), as with many apex predators, equilibrium abundance is not constant across space but rather varies as a function of local habitat quality and resource dynamics, thereby complicating the extrapolation of carrying capacity ( K ) from one location to another. To overcome this challenge, we developed a state‐space model of density‐dependent population dynamics in southern sea otters ( E. l. nereis ), in which K is estimated as a continuously varying function of a suite of physical, biotic, and oceanographic variables, all described at fine spatial scales. We used a theta‐logistic process model that included environmental stochasticity and allowed for density‐independent mortality associated with shark bites. We used Bayesian methods to fit the model to time series of survey data, augmented by auxiliary data on cause of death in stranded otters. Our model results showed that the expected density at K for a given area can be predicted based on local bathymetry (depth and distance from shore), benthic substrate composition (rocky vs. soft sediments), presence of kelp canopy, net primary productivity, and whether or not the area is inside an estuary. In addition to density‐dependent reductions in growth, increased levels of shark‐bite mortality over the last decade have also acted to limit population expansion. We used the functional relationships between habitat variables and equilibrium density to project estimated values of K for the entire historical range of southern sea otters in California, USA, accounting for spatial variation in habitat quality. Our results suggest that California could eventually support 17,226 otters (95% CrI = 9,739–30,087). We also used the fitted model to compute candidate values of optimal sustainable population abundance (OSP) for all of California and for regions within California. We employed a simulation‐based approach to determine the abundance associated with the maximum net productivity level (MNPL) and propose that the upper quartile of the distribution of MNPL estimates (accounting for parameter uncertainty) represents an appropriate threshold value for OSP. Based on this analysis, we suggest a candidate value for OSP (for all of California) of 10,236, which represents 59.4% of projected K .

California↗

USGS2010

Ranking Alaska moose nutrition: Signals to begin liberal antlerless harvests

We focused on describing low nutritional status in an increasing moose ( Alces alces gigas ) population with reduced predation in Game Management Unit (GMU) 20A near Fairbanks, Alaska, USA. A skeptical public disallowed liberal antlerless harvests of this moose population until we provided convincing data on low nutritional status. We ranked nutritional status in 15 Alaska moose populations (in boreal forests and coastal tundra) based on multiyear twinning rates. Data on age-of-first-reproduction and parturition rates provided a ranking consistent with twinning rates in the 6 areas where comparative data were available. Also, short-yearling mass provided a ranking consistent with twinning rates in 5 of the 6 areas where data were available. Data from 5 areas implied an inverse relationship between twinning rate and browse removal rate. Only in GMU 20A did nutritional indices reach low levels where justification for halting population growth was apparent, which supports prior findings that nutrition is a minor factor limiting most Alaska moose populations compared to predation. With predator reductions, the GMU 20A moose population increased from 1976 until liberal antlerless harvests in 2004. During 1997–2005, GMU 20A moose exhibited the lowest nutritional status reported to date for wild, noninsular, North American populations, including 1) delayed reproduction until moose reached 36 months of age and the lowest parturition rate among 36-month-old moose (29%, n = 147); 2) the lowest average multiyear twinning rates from late-May aerial surveys ( x̄ = 7%, SE = 0.9%, n = 9 yr, range = 3–10%) and delayed twinning until moose reached 60 months of age; 3) the lowest average mass of female short-yearlings in Alaska ( x̄ = 155 ± 1.6 [SE] kg in the Tanana Flats subpopulation, up to 58 kg below average masses found elsewhere); and 4) high removal (42%) of current annual browse biomass compared to 9–26% elsewhere in boreal forests. When average multiyear twinning rates in GMU 20A (sampled during 1960–2005) declined to <10% in the mid- to late 1990s, we began encouraging liberal antlerless harvests, but only conservative annual harvests of 61–76 antlerless moose were achieved during 1996–2001. Using data in the context of our broader ranking system, we convinced skeptical citizen advisory committees to allow liberal antlerless harvests of 600–690 moose in 2004 and 2005, with the objective of halting population growth of the 16,000–17,000 moose; total harvests were 7–8% of total prehunt numbers. The resulting liberal antlerless harvests served to protect the moose population's health and habitat and to fulfill a mandate for elevated yield. Liberal antlerless harvests appear justified to halt population growth when multiyear twinning rates average ≤10% and ≥1 of the following signals substantiate low nutritional status: <50% of 36-month-old moose are parturient, average multiyear short-yearling mass is <175 kg, or >35% of annual browse biomass is removed by moose.

Journal of Wildlife Management↗

USGS2015

A broader definition of occupancy: A reply to Hayes and Monofils

Occupancy models are widely used to analyze presence–absence data for a variety of taxa while accounting for observation error (MacKenzie et al. 2002, 2006; Tyre et al. 2003; Royle and Dorazio 2008). Hayes and Monfils (2015) question their use for analyzing avian point count data based on purported violations of model assumptions incurred by avian mobility. Animal mobility is an important consideration, not just for occupancy models, but for a variety of population and habitat models (Boyce 2006, Royle et al. 2009, Manning and Goldberg 2010, Dormann et al. 2013, Renner et al. 2015). Nevertheless, we believe the ultimate conclusions of Hayes and Monfils are shortsighted mainly due to a narrow interpretation of occupancy. Rather than turn away from the use of occupancy models, we believe they remain an appropriate method for analyzing many data sets collected from avian point count surveys. Further, we suggest that there is value in having a broader and more nuanced interpretation of occupancy that incorporates the potential for animal movement.

Journal of Wildlife Management↗

USGS2016

Book review: Advances in reintroduction biology of Australian and New Zealand fauna

Reintroduction, and other forms of moving animals around the landscape, is an estab lished action that has been used in the contexts of mitiga tion, conservation, and salvage. Advances in Reintroduction Biol ogy of Australia n and New Zealand Fauna is more than an update of its pred ecessor (Serena 1995 ). This book not only enumerates advances in reintroduction but also provides a cogent road map for understanding and applying current know ledge, and for developing future strategi es. Review info: Advances in Reintroduction Biology of Australian and New Zealand Fauna. Doug P. Armstrong, Matthew W. Hayward, Dorian Moro, and Philip J. Seddon, editors. 2015. ISBN 978-1486303014. 320 pp.

Journal of Wildlife Management↗