Fighting and accidental injury commonly cause black rhinoceros (rhino; Diceros bicornis) death after release. Smaller reserves and higher conspecific density after release (release density) might increase a rhino's encounter rate with hazards like fenced boundaries and conspecifics. We conducted a science-by-management experiment on the influence of reserve size and release density on rates of movement, association, and injury and death amongst 39 black rhinos during the first 100 days after their release into 4 Namibian and 8 South African reserves ranging in size from 670 ha to 45,000 ha. Association rates were negatively related to reserve size and positively correlated with release density. There was also a negative relationship between the proportion of the reserve traversed by individual rhinos and reserve size. In reserves ≥18,000 ha association rates were consistently zero but became elevated in reserves ≤11,500 ha and at release densities ≤9 km²/rhino. Daily displacement did not increase with increasing reserve size >8,500 ha but in smaller reserves daily displacements indicated higher encounter rates by released rhinos with fenced boundaries. Three rhinos received fight-related injuries requiring intervention and 2 of 4 deaths were fight-related. All injuries and 3 deaths occurred in reserves ≤11,500 ha. Model selection based on Akaike's second-order Information Criterion indicated that the parameter release density alone best explained mortality risk. Traditionally considered risk factors, rhino sex, age, and presence of resident conspecifics, were superseded by the risk posed by releases into smaller reserves. Reserves ≤11,500 ha and release densities ≤9 km²/rhino pose an increasing risk to rhino survivorship and so larger reserves and lower densities than these should be favored as release sites.

The endangered Florida Key deer (Odocoileus virginianus clavium) is endemic to the Lower Florida Keys. In recent years, habitat fragmentation and restricted dispersal have resulted in small, isolated herds on some islands. Recovery biologists proposed translocations to increase the island herds that had declined or remained low; however, efficacy of Key deer translocations had yet to be evaluated. Our objective was to evaluate survival, ranges, reproduction, and dispersal of translocated deer. During 2003–2005, we translocated 39 adult or yearling deer to Sugarloaf (approx. 19 km from trap site; 10 M, 14 F) and Cudjoe (approx. 15 km from trap site; 6 M, 9 F) keys. We kept deer in large, high-fenced holding pens (Sugarloaf = 7.7 ha, Cudjoe = 10.7 ha) on the destination islands for 3–6 months (i.e., soft release). We observed low mortality (n = 6 mortalities) of translocated deer with average annual survival (S) of 0.796 for both sexes. We found translocated deer had larger seasonal ranges than did resident deer (i.e., those located on Big Pine and No Name keys). In evaluating effects of acclimation period on ranges and dispersal, we found no difference in 95% ranges or 50% core areas ≤4 month postrelease versus 4–8 months postrelease. We found, however, postrelease dispersal distances were dependent on time kept in pen. Only 2 of 39 (5%) translocated deer left the destination islands by the end of the study. With high survival and low dispersal indicating success, we credit soft release translocation in establishing deer herds on Sugarloaf and Cudjoe keys. Our data support translocations as an effective strategy for creating sustainable outer-island Key deer herds.

Because of increasing concerns about puma (Puma concolor) attacks on people and the desire to minimize dangerous puma–human encounters while conserving puma populations, we examined spatial and temporal relationships between pumas and people that used Cuyamaca Rancho State Park (CRSP), California, USA. From 2001 to 2003, we studied 10 adult pumas outfitted with Global Positioning System collars. Although number of visitors to CRSP was increasing, no dangerous puma–human encounters were reported during our study. Male and female pumas typically moved short distances during the day (mean of means of individual hourly movements = 168 m and 131 m each hr, respectively) and moved the most at night (mean of means = 690 m and 390 m each hr, respectively). Of 10 pumas, 9 were least active during the day and most active during the evening or at night. In contrast, most visitor use of trails (x̄ = 85%) occurred during the day. Based on puma and human activity patterns, risk of a puma–human encounter was greatest during the evening. Puma prey caches were randomly distributed in relation to trails and park facilities; however, 8 of 33 caches were still within 100 m of a trail and 2 were within 300 m of a facility. Individual puma behavior relative to human activity areas was variable. Some pumas appeared to temporally avoid human activity areas; others used the park randomly in relation to human activity areas; none appeared to be attracted to human activity areas. Pumas that did not show detectable responses to human activity may have been exhibiting some level of habituation; if so, this level of habituation did not result in puma–human conflicts. When human activity peaked during the day, adult male and female pumas were within 100 m of a trail an average of 9% and 19% of the time they were located in the park, respectively. Thus, there were opportunities for puma–human encounters. Management personnel can take a proactive approach to deal with puma–human interactions through education and protocols that help to minimize probability of conflicts; this may provide the best chance for a continued puma presence in habitat used by pumas and people.

The assumption of independent sample units is potentially violated in survival analyses where siblings comprise a high proportion of the sample. Violation of the independence assumption causes sample data to be overdispersed relative to a binomial model, which leads to underestimates of sampling variances. A variance inflation factor, c, is therefore required to obtain appropriate estimates of variances. We evaluated overdispersion in fetal and neonatal mule deer (Odocoileus hemionus) datasets where more than half of the sample units were comprised of siblings. We developed a likelihood function for estimating fetal survival when the fates of some fetuses are unknown, and we used several variations of the binomial model to estimate neonatal survival. We compared theoretical variance estimates obtained from these analyses with empirical variance estimates obtained from data-bootstrap analyses to estimate the overdispersion parameter, c. Our estimates of c for fetal survival ranged from 0.678 to 1.118, which indicate little to no evidence of overdispersion. For neonatal survival, 3 different models indicated that ranged from 1.1 to 1.4 and averaged 1.24–1.26, providing evidence of limited overdispersion (i.e., limited sibling dependence). Our results indicate that fates of sibling mule deer fetuses and neonates may often be independent even though they have the same dam. Predation tends to act independently on sibling neonates because of dam–neonate behavioral adaptations. The effect of maternal characteristics on sibling fate dependence is less straightforward and may vary by circumstance. We recommend that future neonatal survival studies incorporate additional sampling intensity to accommodate modest overdispersion (i.e., = 1.25), which would facilitate a corresponding adjustment in a model selection analysis using quasi-likelihood without a reduction in power. Our computational approach could be used to evaluate sample unit dependence in other studies where fates of individually marked siblings are monitored.

Sodium has many fundamental physiological functions in animals but is rare in boreal ecosystems where moose (Alces alces) thrive. In Québec (Canada), sodium is readily available in aquatic vegetation and in salt pools that form along highways. We do not know if moose are adopting specific behaviors to access sodium sources or if they simply use the sodium sources they encounter during their movements. We tested the hypothesis that moose modify both space and habitat use to gather sodium from salt pools. We expected moose to use salt pools mostly in spring and early summer, when needs are greatest and before aquatic vegetation has fully developed. We fitted 47 moose with Global Positioning System telemetry collars and collected data for 2 to 36 months between 2003 and 2006. We rarely located moose at salt pools (0.12% among the 95,007 locations collected). As we expected, use of salt pools was highest in late spring and in early summer, and we observed a time lag between peak use of salt pools compared to use of lakes and waterways, indicating moose fulfilled their sodium requirements in salt pools before aquatic vegetation was available. Moose selected salt pools over lakes and waterways when these 2 sodium sources were present in their home range and moved rapidly over large distances to reach them. Our results were consistent with moose using salt pools when they are likely to be sodium deficient. Salt pools were less accessible, required long-distance movements, and were located in habitually avoided areas along highways. Elimination of roadside salt pools should be considered among strategies to reduce cervid–vehicle collision risks in boreal environments.

Cause for spatial variation in phenotypic quality of white-tailed deer (Odocoileus virginianus) populations is of great interest to wildlife managers. Relating phenotypic variation of populations to large-scale land-use patterns may provide insight into why populations exhibit spatial variation and elucidate how management can influence population phenotype. We used an information-theoretic approach to relate average antler size of 203 deer populations to composition and structure of the habitat occupied by those populations. We used interspersion, edge, and diversity indices to represent habitat structure and percentage of area in vegetation types to represent habitat composition. Landscape composition was a better predictor of deer population antler size than was landscape structure. Percentages of the management unit in agriculture, pasture, and pine forest were variables commonly found in the region-specific set of best models. Model-averaged estimates of agriculture and pasture parameters were always positive and estimates of pine forest parameters were always negative, which suggests that land-use types that promote growth of early successional herbaceous plants will positively influence antler size and, most likely, body growth and reproduction of white-tailed deer populations. Conversely, our findings suggest landscapes dominated by pine forests did not provide optimal amounts of quality forages for white-tailed deer. Pine forest effects should be mitigated using a combination of increased harvest to lower deer density and silvicultural practices like thinning, prescribed burning, and selective herbicide applications that stimulate growth of high-quality forages beneath the forest canopy to improve deer phenotypic quality.

Past studies using penned deer provide conflicting results on the age when reliable predictions about antler growth potential in white-tailed deer (Odocoileus virginianus) can be made. We captured wild whitetail males via aerial net gun on 12 ranches in 5 counties in south Texas, USA, from 1999 to 2007 to determine if a reliable juvenile-to-adult relationship in antler development existed. We individually marked and released captured animals at the trap site after we took antler and body measurements. We recaptured marked animals as possible in subsequent years or until we obtained final measurements after legal harvest. Amount of growth in the first set of antlers in whitetail males was a poor predictor of antler growth at maturity. By 4.5 years of age there were no differences (P > 0.05) in antler measurements regardless of the amount of development of the first set of antlers at 1.5 years. We concluded culling of yearling males based on number of antler points would have little positive effect on overall antler quality in future years.

Historically, bobcats (Lynx rufus) were found throughout the Corn Belt region, but they nearly disappeared from this area due to habitat loss and unregulated harvest that occurred during the century after European settlement. Reports of bobcat occurrences have been increasing in Iowa, USA, and biologists would like to understand the mechanisms enabling bobcats to recolonize this fragmented agricultural landscape. We determined space use and habitat selection of bobcats by radiocollaring 68 bobcats in south-central Iowa during 2003–2006. We triangulated 12,966 locations and recovered an additional 1,399 3-dimensional locations from Global Positioning System collars. We used a fixed kernel estimator to calculate 95% utilization distributions (UDs) for home ranges and 50% UDs for cores. Annual home range area of males (x̄ = 58.6 km², 95% CI = 49.2–69.9) was nearly 3 times that of females (x̄ = 19.9 km², 95% CI = 17.0–23.3). Females used smaller home ranges during April–September when they were suspected to have kittens with them (x̄ = 16.8 km², 95% CI = 13.7–20.7), as compared to October–March (x̄ = 24.1 km², 95% CI = 19.0–30.7), whereas home ranges of males did not differ between seasons. Similarly, core area of males (x̄ = 7.7 km², 95% CI = 6.2–9.6) was larger than that of females (x̄ = 2.3 km², 95% CI = 1.9–2.7). Females used significantly smaller cores in April–September (x̄ = 1.8 km², 95% CI = 1.4–2.3) as compared to October–March (x̄ = 2.8 km², 95% CI = 2.2–3.7), whereas males did not. For both sexes, compositional analysis indicated that forest habitat was ranked higher than all other habitat classes at both the landscape and local scale. Standardized habitat selection ratios illustrate that female and male bobcats selected forest habitat about twice as frequently as any other habitat class, including grassland and Conservation Reserve Program land. Predictive models indicated that home range and core area was smaller in landscapes where perennial forest and grassland habitats were less fragmented. Predictive models indicated home ranges were more irregular in shape in landscapes where row crop patches were less aggregated within home ranges. Our results have practical implications for wildlife managers regarding expected bobcat habitat use and distribution as the species becomes more abundant in the agricultural landscape of the Midwest.

Population viability analysis (PVA) is a common tool to evaluate population vulnerability. However, most techniques require reliable estimates of underlying population parameters, which are often difficult to obtain and PVA are, therefore, best used in a qualitative context. Logistic regression is a powerful alternative to traditional PVA methods but has received surprisingly limited attention. Logistic regression fits regression equations to binary output from PVA models at a specific point in time to predict probability of a binary response over a range of parameter values. We used logistic regression on output from stochastic population models to evaluate the relative importance of demographic parameters for wolverine (Gulo gulo) populations and to estimate sustainable harvest in a wolverine population in Alaska. Our analysis indicated that adult survival is the most important demographic parameter to reliably estimate in wolverine populations because it had a greater effect on population persistence than did both fecundity and subadult survival. In accordance with this, harvest rate had a greater effect on population persistence than did any of the other harvest- and migration-related variables we tested. Furthermore, a high proportion of harvested females strengthened the effect of harvest. Hypothetical wolverine populations suffered high probabilities of both extinction and population decline over a range of realistic population sizes and harvest regimes. We suggest that harvested wolverine populations must be regarded as sink populations and that source populations in combination with sufficient dispersal corridors must be secured for any wolverine harvest to be sustainable.

Manipulation of forest habitat via mechanical thinning or prescribed fire has become increasingly common across western North America. Nevertheless, empirical research on effects of those activities on wildlife is limited, although prescribed fire in particular often is assumed to benefit large herbivores. We evaluated effects of season and spatial scale on response of Rocky Mountain elk (Cervus elaphus) and mule deer (Odocoileus hemionus) to experimental habitat manipulation at the Starkey Experimental Forest and Range in northeastern Oregon, USA. From 2001 to 2003, 26 densely stocked stands of true fir (Abies spp.) and Douglas-fir (Pseudotsuga menziesii) were thinned and burned whereas 27 similar stands were left untreated to serve as experimental controls. We used location data for elk and mule deer collected during spring (1 Apr–14 Jun) and summer (15 Jun–31 Aug) of 1999–2006 to compare use of treated and untreated stands and to model effects of environmental covariates on use of treated stands. In spring, elk selected burned stands and avoided control stands within the study area (second-order selection; large scale). Within home ranges (third-order selection; small scale), however, elk did not exhibit selection. In addition, selection of treatment stands by elk in spring was not strongly related to environmental covariates. Conversely, in summer elk selected control stands and either avoided or used burned stands proportional to their availability at the large scale; patterns of space use within home ranges were similar to those observed in spring. Use of treatment stands by elk in summer was related to topography, proximity to roads, stand size and shape, and presence of cattle, and a model of stand use explained 50% of variation in selection ratios. Patterns of stand use by mule deer did not change following habitat manipulation, and mule deer avoided or used all stand types proportional to their availability across seasons and scales. In systems similar to Starkey, manipulating forest habitat with prescribed fire might be of greater benefit to elk than mule deer where these species are sympatric, and thus maintaining a mixture of burned and unburned (late successional) habitat might provide better long-term foraging opportunities for both species than would burning a large proportion of a landscape.

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.

During 2 years of radiotelemetry research on chukars (Alectoris chukar) in western Utah, USA, we found 28% of retrieved radios (n = 78) in rubbish nests of woodrats (Neotoma spp.). Such movement and disturbance of carcasses and radios by woodrats and other species has implications for radiotelemetry studies. We evaluated spatio-temporal movement of 51 radiocollars attached to chukar carcasses in western Utah. Most (80%) carcasses were scavenged within one week and by the end of 3 weeks 25 (50%) had been retrieved from woodrat middens. Scavenging activity can both obscure important clues needed to identify causes of mortality and bias telemetry studies by delaying onset of mortality signals.

To focus white-tailed deer (Odocoileus virginianus) management within a chronic wasting disease–infected area in south-central Wisconsin, USA, we assessed deer movements and related dispersal to variation in landscape pattern, deer density, and harvest intensity. We radiocollared and monitored 165 deer between 2003 and 2005. Yearling males that dispersed (45%) had greater forest edge (i.e., fragmentation) within natal home ranges. Exploratory movements were rare for adult females. Transient and migratory movements were rare among all deer (<5%). Although yearling males have low chronic wasting disease prevalence rates, they may be infected before dispersal due to variable incubation times. Managers should increase yearling male harvest and consider removing young males in areas of higher forest edge.

We used radiotelemetry to locate daytime forms of endangered Lower Keys marsh rabbits (LKMRs; Sylvilagus palustris hefneri) throughout their range so we could determine habitat characteristics of diurnal cover. We typically found forms (n = 1,298) of 36 rabbits in brackish wetlands in patches of saltmarsh or buttonwoods. In freshwater wetlands, forms (n = 54) were located most often in patches of freshwater hardwoods embedded in or adjacent to freshwater marshes. Forms (n = 942) in brackish wetlands were characterized by thick groundcover (>75%), whereas those (n = 42) in freshwater wetlands had both thick groundcover and canopy vegetation. The mean minimum convex polygon around forms of 15 rabbits was 1.4 ha (SD = 1.7), with smaller ranges characterized by thick bunchgrasses or clump-forming sedges. To increase the amount of annual space usable by LKMRs, managers should provide more saltmarsh habitat interspersed with buttonwoods and enhance ground cover in existing habitat.

We assessed responses of the breeding bird community to mechanical thinning and prescribed surface fire, alone and in combination, between 2000 and 2006 in ponderosa pine (Pinus ponderosa) forests in northern Arizona, USA. Fuel-reduction treatments did not affect species richness or evenness, and effects on density of 5 commonly detected species varied among species. Populations of some species, such as the western bluebird (Sialia mexicana), increased following burning treatments, whereas others, such as the mountain chickadee (Poecile gambeli), decreased in response to thinning treatments. Our results also identified a temporal response component, where avian community composition and structure changed synchronously on all treatments over time. Given the modest effects these small-scale fuel-reduction treatments had on avian composition and the specific density responses of particular species, our results suggest that land managers should consider implementing prescribed surface fire after thinning projects, where appropriate.

Currently available methods of estimating northern bobwhite (Colinus virginianus) abundance are often expensive and time-consuming; therefore, additional research is necessary to develop new tools. Using Global Positioning System (GPS) and Geographic Information System technologies and distance-sampling theory, we developed a method of estimating bobwhite density during hunts with pointing dogs. Data collection occurred during the 2005–2006 and 2006–2007 hunting seasons in western Oklahoma and northern Texas, USA. We estimated effective strip width (ESW) of a bird dog's path using distance-sampling theory and point-to-flush distances. For coveys >7 birds (n = 58), estimated ESW was 13.2 m (95% CI = 11.1–15.6 m). Area searched by one dog was its GPS path buffered by ESW. For ≥2 dogs, area searched was the union of the areas of individual dogs; taking the union eliminated between- or among-dog redundancy in searched areas. A point estimate of density was number of birds flushed on a hunt divided by searched area. During the 2005–2006 hunting season, bobwhite density averaged 1.4 birds/ha (±0.28 SE; n = 33). Average density declined to 0.2 birds/ha (±0.07 SE) during 2006–2007 (n = 46). Estimating bobwhite density with pointing dogs needs further testing and development, but the technique may prove useful in research and management.

Mallard (Anas platyrhynchos) populations in the United States portion of the Great Lakes region increased through the 1990s but have since declined. To promote sustainable growth of this population, managers need to understand how perturbation of vital rates will affect annual population growth rate (λ). We developed a stage-based model representing the female mallard population in the Great Lakes using vital rates generated from a landscape-level study documenting reproductive parameters from 2001 to 2003. We conducted perturbation analyses (i.e., sensitivity analyses) to identify vital rates that most influence λ and variance decomposition analyses to determine the proportion of variation in λ explained by variation in each vital rate. Perturbation analyses indicated that λ was most sensitive to changes in nonbreeding survival, duckling survival, and nest success. Therefore, changes in these vital rates would be expected to result in the greatest Δλ. Process variation in breeding season parameters accounted for 63% of variation in λ. Breeding season parameters explaining the most variation were duckling survival (32%) and nest success (16%). Survival of adult females outside the breeding season accounted for 36% of variation in λ. Harvest derivation, high harvest, and high sensitivity of λ to nonbreeding survival for Great Lakes female mallards suggests there is a strong potential for managing the Great Lakes mallard population via harvest management. Because λ was highly sensitive to changes in duckling survival, we suggest programs that emphasize wetland protection, enhancement, and restoration as a management strategy to improve population growth for breeding mallards.

We tested whether colony-site availability could allow for an increase in the unusually small breeding populations of yelkouan shearwater (Puffinus yelkouan) on the islands of the Port-Cros National Park (France) if feral cat eradication were undertaken. Comparisons between colony and noncolony sites indicated yelkouan shearwaters preferred deep-soiled and low-outcrop–covered coastal sites. A substrate cover, light avoidance, and sea proximity model suggested that 17.5% of unoccupied sites are suitable for colony establishment. The low proportion of suitable sites currently used by yelkouan shearwaters suggests that these colonies could be refuges and that feral cat eradication will probably lead to a breeding population increase.

Since 1997 the Mexican government has promoted Management Units for Conservation and Sustainable Use of Wildlife (UMAs) on private and community lands as an economically attractive mean for the conservation of biodiversity. To date, compliance of UMAs with stated sustainability goals has not been evaluated. Thus, we designed multicriteria evaluation framework based on the stated objectives of the national UMA program and applied it to a sample of 6 UMAs operating in peasant communities near or in the Calakmul Biosphere Reserve in Campeche, Mexico. Evaluation criteria covered thematic areas of environment, economy, social development, and laws and rules. We formulated 15 criteria with 29 indicators, and 133 verifiers. Data for the verifiers were based on direct observation, interviews with key actors in the peasant communities, participation in regional meetings, scrutiny of government reports, and databases. We calculated sustainability indexes by weighting, summing, and standardizing verifiers to percentage scales, and aggregating to the successive higher hierarchical levels of the evaluation framework. We found an average overall sustainability index of 45.7% for the UMAs evaluated. Scores were highest for the environment thematic area (55.2%), followed by economy (43.4%), social development (42.3%), and laws and rules (41.7%). We observed particularly low indicators for management strategies, habitat monitoring, environmental education, and knowledge of wildlife laws. We conclude that the contribution of UMAs to the conservation and sustainable use of biodiversity could be improved by a number of actions. These include developing wildlife management educational programs with a strong environmental legislation component, the correct enforcement of wildlife laws, and creating country-wise links among academic and governmental institutions promoting the work with regional and national wildlife experts.

A common situation in capture–mark–recapture (CMR) studies on birds and other organisms is to capture individuals not belonging to the studied population only present during the short time of the capture session. Presence of such transient individuals affects demographic parameter estimation from CMR data. Methods exist to reduce biases on survival estimates in the presence of transients and have been shown to be particularly efficient within the Robust Design framework (several secondary capture sessions within a short time interval during which the studied population can be assumed closed). We present a new model to estimate population size accounting for transients. We first used simulated data to show that the method reduces positive biases due to transients. In a second step, we applied the method to a real CMR dataset on a reed warbler (Acrocephalus scirpaceus) population. Population size estimates are reduced by up to 50% when correcting for the presence of transients. Many field studies on managed animal populations use capture–recapture methodology to obtain crucial parameters of the focal population demography. The resulting data sets are used either to estimate population size ignoring the presence of transients, or to estimate vital rates, accounting for transients but overlooking abundance estimation. Our method conciliates these 2 approaches.

Ecologists and wildlife biologists rely on periodic observation of radiocollared animals to study habitat use, survival, movement, and migration, resulting in response times (e.g., mortality and migration) known only to occur within an interval of time. We illustrate methods for analyzing interval-censored data using data on the timing of fall migration (from spring-summer-fall to winter ranges) for white-tailed deer (Odocoileus virginianus) in northern Minnesota, USA, during years 1991–1992 to 2005–2006. We compare both nonparametric and parametric methods for estimating the cumulative distribution function of migration times, and we suggest a parametric (cure rate) model that accounts for conditional (facultative) migrators as a potential alternative to traditional parametric models. Lastly, we illustrate methods for exploring the effect of environmental covariates on migration timing. Models with time-dependent covariates (snow depth, temp) were sensitive to the treatment of the data (as interval-censored or known event times), suggesting the need to account for interval-censoring when modeling the effect of these covariates.

Canada goose (Branta canadensis) harvest management depends on reliable estimates of harvest composition, and established genetic methods provide an alternative to traditional methods. We expanded upon previous genetic studies by comparing the utility of 6 nuclear microsatellite loci and mitochondrial (mtDNA) control region sequences for discriminating among giant (B. c. maxima) and interior (B. c. interior) populations in Ohio (USA) Canada goose harvests at both individual and population levels. Subspecies and populations exhibited greater differentiation in mtDNA (F_ST = 0.202) than microsatellites (F_ST = 0.021), as would be expected based on differences in effective population size. Neither microsatellites nor mtDNA alone were sufficient for estimating harvest composition at the subspecies or population level in simulations and empirical blind tests using individuals of known origin; however, a combined microsatellite mtDNA dataset yielded accurate and precise harvest derivations at the subspecies level. Both population-level mixed stock analysis and individual-level assignment tests provided accurate results, but a large proportion of birds could not be assigned with confidence at the individual level. We applied mixed stock analysis and the combined microsatellite mtDNA dataset to Ohio's 2003–2004 harvest and found that interior populations accounted for 4.9% (95% CI = 1.7–8.0%) of the statewide early season and 9.3% (95% CI = 6.9–11.6%) of the regular and late-season harvested sample. These results suggest that maximum likelihood harvest derivations are highly dependent on the choice of genetic markers. Studies should only employ markers that exhibit sufficient variation and have been shown through simulations and empirical testing to accurately discriminate among the subspecies or management populations of interest.

We determined effectiveness of using mitochondrial DNA barcodes (cytochrome c oxidase subunit 1 [CO1]) to identify bird–aircraft collision (birdstrike) cases that lacked sufficient feather evidence for morphological diagnosis. From September through December 2006, 821 samples from birdstrike events occurring in the United States were submitted for DNA analysis. We successfully amplified a CO1 DNA barcode product from 554 (67.5%) of the samples; 267 (32.5%) did not contain viable DNA and depended on morphological methods (microscopy) for Order or Family level identification. We deemed 19 cases inconclusive either because the DNA barcode recovered from the sample did not meet our 98% match criteria when compared to the Barcode of Life Database (BoLD) or because the DNA barcode matched to a set of ≥2 closely related species with overlapping barcodes, preventing complete species identification. Age of the sample (≤6 months) did not affect DNA viability, but initial condition of the sample and the collection method was critical to DNA identification success. The DNA barcoding approach has great potential in aiding in identification of birds (and wildlife) for airfield management practices, particularly in regions of the world that lack the vast research collections and individual expertise for morphologic identifications.

Certain birds use mammal hair for the lining or structural strengthening of their nest. As a result, many bird nests can be regarded as natural hair snares. Preliminary studies indicate that analyses of hairs found in birds' nests are an effective method for detecting and identifying mammals that live in or migrate through an area and could be a useful tool to gain information about rare or hard to detect mammals. I documented 27 mammal taxa that were identified from hair collected from >3,000 nests. This study summarizes the results of 4 projects that represent application of this technique. This noninvasive method appears to be a useful tool for easily accessing basic faunistical data about mammal fauna of the given area.

We designed and developed a vehicle-mounted very high frequency–based telemetry system that integrated an on-board antenna, receiver, electronic compass, Global Positioning System, computer, and Geographic Information System. The system allows users to accurately and quickly obtain fixes, estimate and confirm locations of radiomarked animals, and immediately record data into an electronic spreadsheet or database. The total cost of materials to build the system was $7,349 (United States currency). Mean error angle of 2.63 ± 12.1° (SD; range = −33.7–42.2°) and mean location error distance of 128 ± 91.3 m (SD; range = 0–408 m) suggested precision and accuracy of our system were comparable to other reported systems. Mean time to record 5 bearings/test transmitter was 6.28 ± 0.24 minutes (SE), which is the most efficient system reported to locate animals in the field. Vehicle-mounted telemetry systems like ours provide additional value to studies that involve tracking highly mobile species because investigators need not take bearings from established receiving stations and because investigators can immediately recognize bounced signals and take additional bearings and optimize accuracy of location estimates.

Questions in population ecology require the study of marked animals, and marks are assumed to be permanent and not overlooked by observers. I evaluated retention through metamorphosis of visual implant elastomer marks in larval salamanders and frogs and assessed error in observer identification of these marks. I found 1) individual marks were not retained in larval wood frogs (Rana sylvatica), whereas only small marks were likely to be retained in larval salamanders (Eurycea bislineata), and 2) observers did not always correctly identify marked animals. Evaluating the assumptions of marking protocols is important in the design phase of a study so that correct inference can be made about the population processes of interest. This guidance should be generally useful to the design of mark–recapture studies, with particular application to studies of larval amphibians.

Wolverines (Gulo gulo) are a rare carnivore and live-capture efforts often comprise a significant component of field research projects. Wolverine studies have used aerial, snowmobile, hand-capture, and live-trap capture techniques. We reviewed existing wolverine live-capture data to evaluate sex-related biases associated with capture technique. We modified round log live traps, developed a new portable wooden live trap, and evaluated effects of live trap type, trap-site selection, and seasonal timing of trapping on wolverine capture success. Aerial capture techniques had a positive bias for capture of male wolverines. Live-capture rates were highest for portable wooden traps and lowest for barrel traps. Trapping success was highest during March when snow conditions were amenable to wolverine travel and temperatures improved bait effectiveness. Traps in corridor habitats were more successful than traps in noncorridor habitats. This difference was more pronounced in environments with rugged topography. We provide guidance for live-trap operation, describe animal handling procedures, and provide detailed instructions for construction of modified round log and portable wooden wolverine live traps. These will benefit future wolverine studies by increasing trap effectiveness and reducing risk of injury and mortality to captured wolverines.

We evaluated a chamber and nose cone method of isoflurane delivery for anesthetizing eastern gray squirrels (Sciurus carolinensis; summer n = 43, winter n = 48) and Allegheny woodrats (Neotoma magister; summer n = 24, winter n = 13) for use when pain or stress was possible from sampling procedures. Mean induction time for squirrels (from beginning of isoflurane administration to safe removal from trap), was 4.63 ± 0.58 minutes. Squirrels awoke more quickly in summer (1.40 ± 0.15 min) than in winter (3.62 ± 0.24 min) after removal of the nose cone. We manually restrained woodrats and administered the nose cone for 0.5 minutes to each animal. Woodrats awoke after 4.76 ± 0.58 minutes following the final dose of isoflurane for both seasons. These methods are useful for working with small mammals in the field and provide an appropriate anesthetic when there may be more than slight pain or distress.

We chemically restrained free-ranging coyotes (Canis latrans), red foxes (Vulpes vulpes), and raccoons (Procyon lotor) using medetomidine antagonized by atipamezole. All coyotes and 80% of red foxes were sedated with mean ± standard deviation doses of 0.12 ± 0.02 mg/kg and 0.14 ± 0.02 mg/kg medetomidine, respectively. Seventy-seven percent of raccoons were sedated with 0.21 ± 0.05 mg/kg medetomidine. In all species we observed occasional movement, muscle rigidity, and partial-arousal during sedation. Animals were alert within 4.3–8.6 ± 3.5–8.4 min following atipamezole at 0.4 mg/kg. Medetomidine and atipamezole provided safe handling in most animals and rapid recovery without use of a controlled substance. At these doses, biologists in the field should be prepared to administer a supplementary dose of medetomidine to some animals depending on ambient conditions and the objectives of the restraint event.

I review concepts of basic graph design and outline general guidance for basic preparation and presentation of data. I comment on the continued use of convenient summary graphics found in our literature where data are often misrepresented and review potential remedies that will improve data description and graphical efficiency for the most frequently used graph types in wildlife data reporting. I suggest that graphics should play a larger role in data description and analysis and less in summarizing study results.