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Monitoring surveys allow managers to document system status and provide the quantitative basis for management decision-making, and large amounts of effort and funding are devoted to monitoring. Still, monitoring surveys often fall short of providing required information; inadequacies exist in survey designs, analyses procedures, or in the ability to integrate the information into an appropriate evaluation of management actions. We describe current uses of monitoring data, provide our perspective on the value and limitations of current approaches to monitoring, and set the stage for 3 papers that discuss current goals and implementation of monitoring programs. These papers were derived from presentations at a symposium at The Wildlife Society's 13th Annual Conference in Anchorage, Alaska, USA.
Population trend data from the North American Breeding Bird Survey (BBS) have been used to identify conservation priorities and justify major conservation initiatives. Yet the BBS has been criticized for potential habitat bias and reliance on abundance indices to estimate trends. We compared 1992–2003 BBS trend estimates to trend estimates derived from bird-banding data collected as part of the Monitoring Avian Productivity and Survivorship (MAPS) program for 36 wood warbler species. Similarity in trends between the 2 monitoring programs at the survey-wide and program-wide scales suggested that each program can provide accurate trend information. The MAPS program, however, was designed primarily to complement (rather than duplicate) count-based efforts, such as the BBS, by providing estimates or indices of demographic rates. Demographic data from MAPS can be used to lend insight into proximate (demographic) causes of population trends and inform management. We illustrate this with analyses of 1992–2003 MAPS data for yellow warbler (Dendroica petechia). We used reverse-time capture–recapture models to evaluate importance of new recruits (including immigrating adults and young from the previous year) relative to surviving adults in explaining variation in trend among BBS physiographic strata. We included the number of young per adult captured (an index of productivity) as a covariate in models to assess effects of productivity on trends. Survival was the key demographic driver of recent population trends. Comparison of MAPS productivity indices and adult apparent survival rate estimates to BBS trend estimates largely confirmed this inference. We suggest that increased MAPS coverage, better coordination between MAPS and the BBS, and continued development of analytical methods that link the 2 programs will enhance the value of these monitoring efforts to land managers and conservation planners working at a variety of spatial scales.
The use of bird counts as indices has come under increasing scrutiny because assumptions concerning detection probabilities may not be met, but there also seems to be some resistance to use of model-based approaches to estimating abundance. We used data from the United States Forest Service, Southern Region bird monitoring program to compare several common approaches for estimating annual abundance or indices and population trends from point-count data. We compared indices of abundance estimated as annual means of counts and from a mixed-Poisson model to abundance estimates from a count-removal model with 3 time intervals and a distance model with 3 distance bands. We compared trend estimates calculated from an autoregressive, exponential model fit to annual abundance estimates from the above methods and also by estimating trend directly by treating year as a continuous covariate in the mixed-Poisson model. We produced estimates for 6 forest songbirds based on an average of 621 and 459 points in 2 physiographic areas from 1997 to 2004. There was strong evidence that detection probabilities varied among species and years. Nevertheless, there was good overall agreement across trend estimates from the 5 methods for 9 of 12 comparisons. In 3 of 12 comparisons, however, patterns in detection probabilities potentially confounded interpretation of uncorrected counts. Estimates of detection probabilities differed greatly between removal and distance models, likely because the methods estimated different components of detection probability and the data collection was not optimally designed for either method. Given that detection probabilities often vary among species, years, and observers investigators should address detection probability in their surveys, whether it be by estimation of probability of detection and abundance, estimation of effects of key covariates when modeling count as an index of abundance, or through design-based methods to standardize these effects.
In a natural resource management setting, monitoring is a crucial component of an informed process for making decisions, and monitoring design should be driven by the decision context and associated uncertainties. Monitoring itself can play ≥3 roles. First, it is important for state-dependent decision-making, as when managers need to know the system state before deciding on the appropriate course of action during the ensuing management cycle. Second, monitoring is critical for evaluating the effectiveness of management actions relative to objectives. Third, in an adaptive management setting, monitoring provides the feedback loop for learning about the system; learning is sought not for its own sake but primarily to better achieve management objectives. In this case, monitoring should be designed to reduce the critical uncertainties in models of the managed system. The United States Geological Survey and United States Fish and Wildlife Service are conducting a large-scale management experiment on 23 National Wildlife Refuges across the Northeast and Midwest Regions. The primary management objective is to provide habitat for migratory waterbirds, particularly during migration, using water-level manipulations in managed wetlands. Key uncertainties are related to the potential trade-offs created by management for a specific waterbird guild (e.g., migratory shorebirds) and the response of waterbirds, plant communities, and invertebrates to specific experimental hydroperiods. We reviewed the monitoring program associated with this study, and the ways that specific observations fill ≥1 of the roles identified above. We used observations from our monitoring to improve state-dependent decisions to control undesired plants, to evaluate management performance relative to shallow-water habitat objectives, and to evaluate potential trade-offs between waterfowl and shorebird habitat management. With limited staff and budgets, management agencies need efficient monitoring programs that are used for decision-making, not comprehensive studies that elucidate all manner of ecological relationships.
We present the first rigorous estimate of grizzly bear (Ursus arctos) population density and distribution in and around Glacier National Park (GNP), Montana, USA. We used genetic analysis to identify individual bears from hair samples collected via 2 concurrent sampling methods: 1) systematically distributed, baited, barbed-wire hair traps and 2) unbaited bear rub trees found along trails. We used Huggins closed mixture models in Program MARK to estimate total population size and developed a method to account for heterogeneity caused by unequal access to rub trees. We corrected our estimate for lack of geographic closure using a new method that utilizes information from radiocollared bears and the distribution of bears captured with DNA sampling. Adjusted for closure, the average number of grizzly bears in our study area was 240.7 (95% CI = 202–303) in 1998 and 240.6 (95% CI = 205–304) in 2000. Average grizzly bear density was 30 bears/1,000 km2, with 2.4 times more bears detected per hair trap inside than outside GNP. We provide baseline information important for managing one of the few remaining populations of grizzlies in the contiguous United States.
I investigated seasonal altitudinal movements of 42 mountain goats (Oreamnos americanus) in the Cascade Range of Washington, USA. Because mountain goats typically move to lower elevations during the winter, I partitioned locations from Global Positioning System collars into summer and winter seasons based on elevation. Using an iterative narrowing search, I identified summer and winter start dates for each individual and year and derived several measures of altitudinal movements from these, and examined differences in these measures on the basis of sex and year and their interrelationship. Generally, female mountain goats started summer about 2 weeks earlier than nondispersing males; winter start dates varied among years. Horizontal distance moved between seasons was unrelated to measures of altitudinal movement. Based on elevation, winters were generally longer than summers for mountain goats I studied, suggesting that the common perception of mountain goats as inhabitants of alpine and subalpine terrain is biased, because they spent the greater part of the year at lower elevations. Mountain goats showed a wide range of responses to seasonal environmental changes and individuals cannot be easily classified as migratory or nonmigratory. Because ecological conditions in mountain environments are closely related to elevation and horizontal and altitudinal movements were unrelated, studies of seasonal movements of mountain animals based on horizontal movement may be misleading. Because seasonal altitudinal movements of mountain goats are highly variable, the management needs of each population must be considered separately.
We compared historic (1985–1992) and contemporary (2003–2006) black bear (Ursus americanus) den locations in Rocky Mountain National Park (RMNP), Colorado, USA, for habitat and physiographic attributes of den sites and used maximum entropy modeling to determine which factors were most influential in predicting den-site locations. We observed variability in the relationship between den locations and distance to trails and elevation over time. Locations of historic den sites were most associated with slope, elevation, and covertype, whereas contemporary sites were associated with slope, distance to roads, aspect, and canopy height. Although relationships to covariates differed between historic and contemporary periods, preferred den-site characteristics consistently included steep slopes and factors associated with greater snow depth. Distribution of den locations shifted toward areas closer to human developments, indicating little negative influence of this factor on den-site selection by black bears in RMNP.
Although domestic animal transmission of rabies has largely been mitigated, the disease remains a concern in both Europe and North America where wildlife transmission has caused epizootics. Raccoon (Procyon lotor) rabies was established in Alabama, USA, in 1975, primarily in the southeastern corner of the state. However, with the exception of isolated events, rabies has not continued to spread westward across the Alabama River. We monitored movements of 100 radiocollared raccoons on 2 sites within hardwood and agriculture habitats in a rabies enzootic area east of the Alabama River, in managed pine habitat area west of the river where rabies sporadically occurs, and in a mixed pine hardwood area outside of the known rabies enzootic area to determine if raccoon movements and habitat use in certain habitat types and the presence of a river may serve as natural barriers preventing the western spread of rabies in Alabama. We also examined raccoon contact rates to determine if they influence disease transmission through static and dynamic interactions. Raccoons in mixed pine–hardwood forest habitats had smaller home ranges and less overlap of ranges compared to the other 3 habitats. However, static interactions between habitats in the use of overlap areas did not differ (F11,129 = 1.63, P = 0.09). Rabies antibody titers were highest in the managed pine habitat (28%) even prior to oral vaccine bait distributions in spring of 2004 and 2005. Biomarker data from radiocollared and additional raccoons captured after the bait distribution west of the Alabama River demonstrated a low efficacy of the vaccine reaching the small southern raccoons. The combination of the river as a partial barrier, the high percentage of pine forested habitat west of the river, and limited spatial movements of raccoons within these forested habitats appears to have reduced the likelihood of rabies establishing west of the river. Understanding different host–habitat–disease systems is important for successful management of diseases. Based on our results, we recommend that the oral vaccine program continue to use the Alabama River as a partial barrier and baiting be concentrated in the fragmented bottomland hardwood forests and around larger bodies of water where raccoon densities are highest. Success of baiting strategies designed to take advantage of northern raccoon dynamics and habitat use may not be applicable to southern populations.
Livestock grazing is common and widespread throughout North America, yet few studies have evaluated its effects on small mammals. We studied small mammals in mixed-conifer forests and oak woodlands on the Cascade–Siskiyou National Monument in southern Oregon, USA, to 1) evaluate small-mammal microhabitat associations, 2) identify riparian-associated species, and 3) test the hypothesis that grazing does not influence small mammals after accounting for microhabitat associations. We live-trapped small mammals at 16 study sites and used logistic regression to model probability of capture on measured habitat characteristics at each trap station and to evaluate effects of grazing. Over 2 years, we trapped 1,270 individual small mammals representing 18 species. Odds of capturing western harvest mice (Reithrodontomys megalotis), dusky-footed woodrats (Neotoma fuscipes), and long-tailed voles (Microtus longicaudus) were lower (P < 0.05) on heavily versus lightly grazed sites. Odds of capture for deer mice (Peromyscus maniculatus) were lower (P < 0.05) on heavily versus lightly grazed sites in woodlands, but there was less difference in the odds of capture between grazing intensities in conifer forests. Odds of capturing Townsend's vole (Microtus townsendii) were lower on heavily versus lightly grazed riparian areas. Western harvest mice, long-tailed voles, and Townsend's voles were associated with, but not obligated to, riparian areas. Deer mice were ubiquitous, but captures were also higher (P < 0.05) in riparian areas compared with uplands. Siskiyou chipmunks (Tamias siskiyou) and piñon mice (Peromyscus truei) were associated with uplands (P < 0.05) rather than riparian areas. Trowbridge's shrews (Sorex trowbridgii), Siskiyou chipmunks, and bushy-tailed woodrats (Neotoma cinerea) were positively associated with coarse woody debris. Land managers should anticipate that small mammals associated with herbaceous or shrub cover, particularly in riparian areas, will decline when cattle remove this cover.
We studied the effects of 6 green-tree retention levels and patterns on the diets of northern flying squirrels (Glaucomys sabrinus), Townsend's chipmunks (Tamias townsendii), Siskiyou chipmunks (T. siskiyou), western red-backed voles (Myodes californicus), and southern red-backed voles (Myodes gapperi) using fecal pellet analysis. These rodents are truffle spore dispersers and prey for forest predators such as the northern spotted owl (Strix occidentalis caurina). Pretreatment diets showed differences in truffle and plant consumption among genera. Tree harvesting, especially in the 15% aggregated retention pattern, reduced frequency of Rhizopogon spores in the diet of voles, which may reflect a reduced ability of these animals to forage for Rhizopogon truffles, a decreased access to these truffles, or a reduction in Rhizopogon truffle abundance or frequency. Habitat island effects and edge effects provide conceptual frameworks for the reduction in consumption of Rhizopogon truffles by voles in green-tree aggregates. Overall, small mammal consumption of truffles showed little change in response to the treatments. Animals may be compensating for a locally declining food source by altering their foraging behavior. The long-term effect of this postulated behavioral compensation on small mammal energetics and population dynamics is unknown. Forest managers may reduce the impact of tree harvesting on these key forest ecosystem components by including green-tree aggregates within a dispersed retention matrix.
Understanding year-round roost-site selection is essential for managing forest bat populations. From January to March, 2004 to 2006, we used radiotelemetry to investigate winter roost-site selection by Seminole bats (Lasiurus seminolus) on an intensively managed landscape with forested corridors in southeastern South Carolina, USA. We modeled roost-site selection with logistic regression and used Akaike's Information Criterion for small samples (AICc) and Akaike weights to select models relating roost-site selection to plot- and landscape-level variables. We tracked 20 adult male bats to 71 individual roosts. Bats used a variety of roosting structures, including the canopy of overstory trees, understory vegetation, pine (Pinus spp.) needle clusters, and leaf litter. Roost height, structure type, and habitat type were influenced by changes in minimum nightly temperature. On warmer nights, bats selected taller trees in mature forest stands, but when minimum nightly temperatures were <4° C, bats typically were found roosting on or near the forest floor in mid-rotation stands. We recommend avoiding prescribed burning in mid-rotation stands on days when the previous night's temperature is <4 °C to minimize potential disturbance and direct mortality of bats roosting on or near the forest floor. We encourage forest managers to incorporate seasonal changes in roost-site selection to create year-round management strategies for forest bats in managed landscapes.
Nest success is an important parameter affecting population fluctuations of wild turkeys (Meleagris gallopavo). Factors influencing mammalian predation on turkey nests are complicated and not well understood. Therefore, we assessed nest hazard risk by testing competing hypotheses of Merriam's turkey (M. g. merriami) nest survival in a ponderosa pine (Pinus ponderosa) ecosystem during 2001–2003. We collected nesting information on 83 female Merriam's turkeys; annual nest success averaged 50% for adult females (range = 45–59%) and 83% for yearling females (range = 75–100%). Proportional hazard modeling indicated that precipitation increased the hazard of nest mortality. However, estimated hazard of nest predation was lowered when incubating females had greater shrub cover and visual obstruction around nests. Coyotes (Canis latrans) were the primary predator on turkey nests. We hypothesize that precipitation is the best predictor of nest survival for first nests because coyotes use olfaction effectively to find nesting females during wet periods. Temporally, as the nesting season progressed, precipitation declined and vegetation cover increased and coyotes may have more difficulty detecting nests under these conditions later in the nesting period. The interaction of concealment cover with precipitation indicated that nest hazard risk from daily precipitation was reduced with greater shrub cover. Management activities that promote greater shrub cover may partially offset the negative effects of greater precipitation events.
We studied how human use of trails affected foraging shorebirds over 24 months at 3 locations around San Francisco Bay, California, USA. By observing sites with trails and nearby sites without trails, we assessed whether numbers of trail users had an effect on the number of birds, species richness, or proportion of shorebirds foraging on tidal mudflats. Human use at non-trail sites averaged <1 person/hour, whereas use at trail sites averaged 68 people/hour. Despite these differences, we found no negative effects of trail use on the number of birds, species richness, or proportion of birds foraging, either overall or by season, when comparing trail to non-trail sites. Human use of trail sites on higher use days (typically weekends) averaged about 2.5 times the level on lower use days (typically weekdays). When comparing bird response on paired lower and higher use days at the trail sites, we found the number of shorebirds decreased with increasing trail use (F1,119 = 4.20, P = 0.043), with higher trail-use days averaging 25% fewer birds than on lower use days. Although managers may allow human use of trails adjacent to shorebird foraging areas under some conditions, high levels of trail use may negatively affect birds, making it essential to offer birds alternative, trail-free foraging opportunities.
King eider (Somateria spectabilis) populations have declined markedly in recent decades for unknown reasons. Nest survival is one component of recruitment, and a female's chance of reproductive success increases with her ability to choose an appropriate nesting strategy. We estimated variation in daily nest survival of king eiders at 2 sites, Teshekpuk and Kuparuk, Alaska, USA, 2002–2005. We evaluated both a priori and exploratory competing models of nest survival that considered importance of nest concealment, seclusion, and incubation constancy as strategies to avoid 2 primary egg predators, avian (Larus spp., Stercorarius spp., and Corvus corax) and fox (Alopex lagopus). We used generalized nonlinear techniques to examine factors affecting nest survival rates and information-theoretic approaches to select among competing models. Estimated nest survival, accounting for a nest visitation effect, varied considerably across sites and years (0.21–0.57); however, given our small sample size, much of this variation may be attributable to sampling variation (σ2process = 0.007, 95% CI: 0.003–0.070). Nest survival was higher at Kuparuk than Teshekpuk in all years; however, due to the correlative nature of our data, we cannot determine the underlying causes with any certainty. We found mixed support for the concealed breeding strategy; females derived no benefit from nesting in areas with more willow (Salix spp.; measure of concealment) except that the observer effect diminished as willow cover increased. We suggest these patterns are due to conflicting predation pressures. Nest survival was not higher on islands (measure of seclusion) or with increased incubation constancy but was higher post–fox removal, indicating that predator control on breeding grounds could be a viable management option. Nest survival was negatively affected by our nest visitations, most likely by exposing the nest to avian scavengers. We recommend precautions be taken to limit the effects of nest visits in future studies and to consider them as a possible negative bias in estimated nest survival. Future models of the impacts of development within the breeding grounds of king eider should consider the influence of humans in the vicinity of nests.
Waterfowl nesting in annual croplands has remained a little-known aspect of waterfowl nesting ecology because of the inability of many studies to systematically search this habitat through the nesting season. Where searches have been conducted, they are generally restricted to the period prior to seeding, and many nests found are destroyed by the seeding operation. Consequently, fall-seeded crops have been promoted as an alternative cropping practice that could increase nest survival of waterfowl nesting in croplands. During 1996–1999, we conducted 3–4 complete nest searches on 4,274 ha of cropland, including spring-seeded wheat and barley, winter wheat, and fall rye in southern Saskatchewan, Canada. Using suites of predictive models, we tested hypotheses regarding relative nest abundance and nest survival among crop types and tested the influence of several landscape-scale covariates on these metrics. Apparent nest densities were higher in fall-seeded crops (winter wheat: 0.39 nests/ha, fall rye: 0.25 nests/ha) than in spring-seeded crops (0.03 nests/ha), and nest density in spring-seeded croplands increased with percent cropland and percent wetland habitat in the surrounding landscape. Nest survival was higher in winter wheat (38%) than in either fall rye (18%) or spring-seeded crops (12%), and nest survival in spring-seeded crops increased with relative nest initiation date. Nest survival was unaffected by surrounding landscape characteristics but tended to be higher in years of average wetness. Based on our findings, winter wheat and fall rye have the potential to provide productive nesting habitat for ≥7 species of upland nesting ducks and fall-seeded crops are a conservation tool well suited to highly cropped landscapes.
Stratification is commonly used to improve sampling efficiency of aerial surveys of ungulate populations with strata typically based on a priori information, such as preflight animal observations or vegetation attributes as surrogates for animal densities. We evaluated the usefulness of stratifying survey units for elk (Cervus elaphus) in the Rocky Mountain foothills of Alberta, Canada, using a resource selection function (RSF). We compared precision and design efficiency (DEFF) of population estimates from stratification approaches based on an RSF model to the past approach using amount of forest cover. We used a sample of telemetry relocations taken over a 3-year period from 165 elk, rarified to times of the day and months of the year when aerial surveys are conducted, to develop the RSF. We then used the top RSF model, based on Akaike's Information Criterion, to derive the average RSF value for an 8-km2 survey unit. Using survey data from the first year, we evaluated binning schemes to define RSF-oriented strata based on poststratification and showed that Jenks natural breaks in the RSF values provided the greatest improvement in DEFF and increased precision, compared to 2 other stratification schemes. We then used this approach with data from 2 additional surveys to find that stratification by RSF consistently improves relative precision and design efficiency of elk population estimates, whether we employ pre- or poststratification. Where a RSF is available it could be used as a surrogate for animal densities when conducting stratified sampling for population surveys.
The traditional method of sex identification in beavers (Castor canadensis) by external palpation can be inaccurate. We tested 2 genetic methods for determining sex in beavers, the zinc-finger DNA marker and the Y chromosome–specific sex determining region (SRY) marker. The SRY marker identified sex correctly in 57 of 67 (85%) beavers, whereas the zinc-finger technique was successful less often in only 48 of 67 (72%) animals. Sex was correctly assigned by palpation for 21 of 27 beavers (78%). Beaver studies in which accurate sex identification is critical may benefit by verifying the sex of individuals using one or both of these molecular markers.
We evaluated the ability of a set of published trans-species molecular sexing primers and a set of walrus-specific primers, which we developed, to accurately identify sex of 235 Pacific walruses (Odobenus rosmarus divergens). The trans-species primers were developed for mammals and targeted the X- and Y-gametologs of the zinc finger protein genes (ZFX, ZFY). We extended this method by using these primers to obtain sequence from Pacific and Atlantic walrus (O. r. rosmarus) ZFX and ZFY genes to develop new walrus-specific primers, which yield polymerase chain reaction products of distinct lengths (327 and 288 base pairs from the X- and Y-chromosome, respectively), allowing them to be used for sex determination. Both methods yielded a determination of sex in all but 1–2% of samples with an accuracy of 99.6–100%. Our walrus-specific primers offer the advantage of small fragment size and facile application to automated electrophoresis and visualization.
Home-range estimators are commonly tested with simulated animal locational data in the laboratory before the estimators are used in practice. Although kernel density estimation (KDE) has performed well as a home-range estimator for simulated data, several recent studies have reported its poor performance when used with data collected in the field. This difference may be because KDE and other home-range estimators are generally tested with simulated point locations that follow known statistical distributions, such as bivariate normal mixtures, which may not represent well the space-use patterns of all wildlife species. We used simulated animal locational data of 5 point pattern shapes that represent a range of wildlife utilization distributions to test 4 methods of home-range estimation: 1) KDE with reference bandwidths, 2) KDE with least-squares cross-validation, 3) KDE with plug-in bandwidths, and 4) minimum convex polygon (MCP). For the point patterns we simulated, MCP tended to produce more accurate area estimates than KDE methods. However, MCP estimates were markedly unstable, with bias varying widely with both sample size and point pattern shape. The KDE methods performed best for concave distributions, which are similar to bivariate normal mixtures, but still overestimated home ranges by about 40–50% even in the best cases. For convex, linear, perforated, and disjoint point patterns, KDE methods overestimated home-range sizes by 50–300%, depending on sample size and method of bandwidth selection. These results indicate that KDE does not produce home-range estimates that are as accurate as the literature suggests, and we recommend exploring other techniques of home-range estimation.
White-tailed deer (Odocoileus virginianus) are important game mammals and potential reservoirs of diseases of domestic livestock; thus, diseases of deer are of great concern to wildlife managers. Contact, either direct or indirect, is necessary for disease transmission, but we know little about the ecological contexts that promote intrasexual contact among deer. Using pair-wise direct contacts estimated from Global Positioning System collar locations and joint utilization distributions (JUDs), we assessed habitats in which contacts occur to test whether direct contact rates among female white-tailed deer in different social groups differs among land-cover types. We also tested whether contact rates differed among seasons, lunar phases, and times of day. We obtained locations from 27 female deer for periods of 0.5–17 months during 2002–2006. We designated any simultaneous pair of locations for 2 deer <25 m apart as a direct contact. For each season, we used compositional analysis to compare land-cover types where 2 deer had contact to available land-cover weighted by their JUD. We used mixed-model logistic regression to test for effects of season, lunar phase, and time of day on contact rates. Contact rates during the gestation season were greater than expected from random use in forest and grassland cover, whereas contact rates during the fawning period were greater in agricultural fields than in other land-cover types. Contact rates were greatest during the rut and lowest in summer. Diel patterns of contact rates varied with season, and contact rates were elevated during full moon compared to other lunar periods. Both spatial and temporal analyses suggest that contact between female deer in different social groups occurs mainly during feeding, which highlights the potential impact of food distribution and habitat on contact rates among deer. By using methods to associate contacts and land-cover, we have created beneficial tools for more elaborate and detailed studies of disease transmission. Our methods can offer information necessary to develop spatially realistic models of disease transmission in deer.
The secretive nature of snow leopards (Uncia uncia) makes them difficult to monitor, yet conservation efforts require accurate and precise methods to estimate abundance. We assessed accuracy of Snow Leopard Information Management System (SLIMS) sign surveys by comparing them with 4 methods for estimating snow leopard abundance: predator:prey biomass ratios, capture–recapture density estimation, photo-capture rate, and individual identification through genetic analysis. We recorded snow leopard sign during standardized surveys in the SaryChat Zapovednik, the Jangart hunting reserve, and the Tomur Strictly Protected Area, in the Tien Shan Mountains of Kyrgyzstan and China. During June–December 2005, adjusted sign averaged 46.3 (SaryChat), 94.6 (Jangart), and 150.8 (Tomur) occurrences/km. We used counts of ibex (Capra ibex) and argali (Ovis ammon) to estimate available prey biomass and subsequent potential snow leopard densities of 8.7 (SaryChat), 1.0 (Jangart), and 1.1 (Tomur) snow leopards/100 km2. Photo capture–recapture density estimates were 0.15 (n = 1 identified individual/1 photo), 0.87 (n = 4/13), and 0.74 (n = 5/6) individuals/100 km2 in SaryChat, Jangart, and Tomur, respectively. Photo-capture rates (photos/100 trap-nights) were 0.09 (SaryChat), 0.93 (Jangart), and 2.37 (Tomur). Genetic analysis of snow leopard fecal samples provided minimum population sizes of 3 (SaryChat), 5 (Jangart), and 9 (Tomur) snow leopards. These results suggest SLIMS sign surveys may be affected by observer bias and environmental variance. However, when such bias and variation are accounted for, sign surveys indicate relative abundances similar to photo rates and genetic individual identification results. Density or abundance estimates based on capture–recapture or ungulate biomass did not agree with other indices of abundance. Confidence in estimated densities, or even detection of significant changes in abundance of snow leopard, will require more effort and better documentation.
Current techniques for remotely monitoring wildlife lack the capability to survey a wide area or to transmit data in real time. We addressed these technology gaps by developing and testing a new video and telemetry system for remotely sampling wildlife abundance, distribution, and behavior across large open areas. The system consisted of 2 pan–tilt–zoom video cameras equipped with 20–200× lens, and an automated telemetry scanner and data logger. All components were charged by wind and solar power and located on a hilltop overlooking an open valley (23 km2) in Yellowstone National Park, USA. A satellite up-link to the internet transmitted data in real time to the University of Minnesota-St. Paul and relayed commands from undergraduate students who controlled the cameras and systematically scanned the area at 2-hour intervals 6 times/day (0800–2000 hr) 7 days/week for about 20 consecutive weeks (Dec–Jun). During each scan, students recorded presence, activity, and location of bison (Bison bison), coyote (Canis latrans), grizzly bear (Ursus arctos), red fox (Vulpes vulpes), and wolf (Canis lupus). The telemetry system continuously scanned frequencies of 100 tagged wolves, including 4 members of the one resident pack. We determined wolf presence in real time by viewing the incoming data stream, or we assessed presence later after off-loading the data logger. Matched pairs of simultaneous observations taken by remote and on-site observers during a 13-day double-sampling period were highly correlated (r = 0.71–0.94), but remote observations were biased toward larger, more visible mammals (e.g., bison) and tended to underestimate their abundance. Nevertheless, the system was deployed longer than was practical for on-site observers and was, therefore, useful for detecting long-term, fine-scale trends such as daily changes in bison numbers as a function of snow depth.
Accurately predicting occurrence of wildlife damage is crucial for effective management of problematic wildlife species, because accurate predication allows deterrence efforts to be focused at sites or times where damage is most likely. We explored methods to predict occurrence of white-fronted geese (Anser albifrons) grazing in wheat fields around Lake Miyajimanuma, Japan. Depletion of waste rice grains caused geese to forage on wheat leaves in spring, reducing wheat harvest in grazed fields. The cumulative number of goose-days per hectare of rice-planted area from the beginning of the staging period explained the variation in the proportion of geese foraging in wheat fields. A logistic regression model on the location of vulnerable fields showed that goose grazing was likely to occur in wheat fields far from roads and windbreaks and those close to (within 1,000–2,000 m of) previously grazed fields. Although probability of occurrence of goose grazing was initially low in wheat fields with scaring devices, effectiveness of such devices was lost over the 4 survey years. We recommend farmers in the study area prepare counter-damage measures when the cumulative number of goose-days per rice-planted area approaches a threshold above which some geese are predicted to start foraging on wheat (e.g., 199.46 goose-days/ha rice ± 28.95 for 10% of geese foraging on wheat). Further, farmers should be aware that grazing on wheat is more likely to occur if wheat fields within 1,000–2,000 m have already been exploited during that particular season and should concentrate deterrence efforts to wheat fields that are far from roads and windbreaks. Systematic deployment of scaring devices over the entire habitat has a risk of accelerating the decline in effectiveness. Thus, we need methods to retard goose habituation to scaring devices, such as scaring with guns, providing alternative feeding sites, and preventing diet change by geese.
Management and conservation of large carnivores increasingly includes conflicts with humans. Consequently, a greater understanding of spatiotemporal trends of conflicts is needed to efficiently allocate resources and apply targeted management. Therefore, we examined spatial and temporal distribution of American black bear (Ursus americanus; hereafter, bear)–human conflicts in Colorado, USA, related to 3 conflict types (agriculture operations, human development, and road kills). We used the Getis–Ord spatial clustering statistic to describe location and assess magnitude of bear–human conflicts in Colorado during 1986–2003 and investigated temporal trends of bear–human conflicts by type. Bear–human conflicts showed distinct spatial clustering by type, and areas of high clustering overlapped conflict types. Clustering for agriculture operations conflicts had the largest overall value and overlapped counties with high sheep production. Both human development and road-kill conflict clusters were high in areas of high-quality oak (Quercus spp.)–shrub habitat in the central and southern portions of Colorado's Front Range region and near the city of Durango in southwestern Colorado. Bear–human conflicts varied by year and type but overall increased during the 18 years. Summed across years, most conflicts were related to agriculture (32%), followed by road kills (27%) and human development (24%). The greatest proportion of agriculture operations–related conflicts (76%), human development–related conflicts (36%), and road kills (47%) occurred in 1988, 1999, and 2003, respectively. Considering that bear–human conflicts in Colorado increased over time and will likely continue to increase, we suggest wildlife managers improve data collection by obtaining detailed location data, categorizing conflict types uniformly, and applying conflict regulations consistently to strengthen inference of similar analyses. We also suggest that managers target efforts to mitigate damage by focusing on areas with high clustering of conflicts.
Nonlethal management alternatives are needed to minimize bird depredation of agricultural crops. We conducted 8 caged feeding tests and 2 field studies to evaluate 2 registered fungicides (GWN-4770, Gowan Company, Yuma, AZ; Quadris®, Syngenta Crop Protection, Greensboro, NC), a neem oil insecticide (Aza-Direct®, Gowan Company), and a novel terpene formulation (Gander Gone, Natural Earth Products, Winter Springs, FL) as avian repellents. For all candidate repellents, red-winged blackbirds (Agelaius phoeniceus) discriminated between untreated and treated rice during preference-testing in captivity. We observed a positive concentration–response relationship among birds offered rice treated with 2,500 ppm, 5,000 ppm, 7,500 ppm, 11,000 ppm, or 22,000 ppm GWN-4770. Relative to pretreatment, blackbirds consumed 34% and 77% less rice treated with 11,000 ppm and 22,000 ppm GWN-4770, respectively, during the concentration–response test. Maximum repellency among other tested compounds was <40% during the concentration–response test. Blackbirds consumed 28% of rice seeds treated with 20,000 ppm GWN-4770 and 68% of untreated seeds broadcast within rice fields in southwestern Louisiana, USA. We observed 50% fewer unprotected seedlings than those treated with 10,000 ppm GWN-4770 within a drill-seeded rice field in southeastern Missouri, USA. The manufacturer subsequently applied for a United States patent for the active ingredient of GWN-4770 as an avian repellent. Although additional registration criteria and formulation optimization must be satisfied to enable the commercial availability of GWN-4770 as an avian repellent, additional efficacy studies of GWN-4770 and other promising repellents under extended field conditions are warranted for protection of newly planted and ripening rice.
Statistics is one of the most important yet difficult subjects for many ecology and wildlife graduate students to learn. Insufficient knowledge about how to conduct quality science and the ongoing debate about the relative value of competing statistical ideologies contribute to uncertainties among graduate students regarding which statistical tests are most appropriate. Herein, we argue that increased education of the available statistical tests alone is unlikely to ameliorate the problem. Instead, we suggest that statistical uncertainties among graduate students are a secondary symptom of a larger problem. We believe the root cause lies in the lack of education on how to conduct science as an integrated process from hypothesis creation through statistical analysis. We argue that if students are taught to think about how each step of the process will affect all other steps, many statistical uncertainties will be avoided.
I hypothesized that statistical ritual has supplanted knowledge accrual as the sine qua non of wildlife science. Under the hypothesis, I deduced occurrence of 1) significance testing of the obvious and inconsequential, 2) quantitative debasement of research problems, and 3) publication of papers that largely lacked information but were methodologically impeccable. Articles in past and recent wildlife literature fit the deductions and supported the hypothesis. Thus, wildlife science is operating inefficiently because quantitative formalities are supplanting ecological information in technical articles. This problem can be corrected by a change of mindset in authors, referees, and editors. The change entails less emphasis on quantitative ritual and more emphasis on information that aids in understanding and explaining nature and managing wildlife.
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