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At least 1,243 records · Page 69Linked to original sources

USGS2014

Dietary breadth of grizzly bears in the Greater Yellowstone Ecosystem

Grizzly bears ( Ursus arctos ) in the Greater Yellowstone Ecosystem (GYE) are opportunistic omnivores that eat a great diversity of plant and animal species. Changes in climate may affect regional vegetation, hydrology, insects, and fire regimes, likely influencing the abundance, range, and elevational distribution of the plants and animals consumed by GYE grizzly bears. Determining the dietary breadth of grizzly bears is important to document future changes in food resources and how those changes may affect the nutritional ecology of grizzlies. However, no synthesis exists of all foods consumed by grizzly bears in the GYE. We conducted a review of available literature and compiled a list of species consumed by grizzly bears in the GYE. We documented >266 species within 200 genera from 4 kingdoms, including 175 plant, 37 invertebrate, 34 mammal, 7 fungi, 7 bird, 4 fish, 1 amphibian, and 1 algae species as well as 1 soil type consumed by grizzly bears. The average energy values of the ungulates (6.8 kcal/g), trout (Oncorhynchus spp., 6.1 kcal/g), and small mammals (4.5 kcal/g) eaten by grizzlies were higher than those of the plants (3.0 kcal/g) and invertebrates (2.7 kcal/g) they consumed. The most frequently detected diet items were graminoids, ants (Formicidae), whitebark pine seeds (Pinus albicaulis), clover (Trifolium spp.), and dandelion (Taraxacum spp.). The most consistently used foods on a temporal basis were graminoids, ants, whitebark pine seeds, clover, elk (Cervus elaphus), thistle (Cirsium spp.), and horsetail (Equisetum spp.). Historically, garbage was a significant diet item for grizzlies until refuse dumps were closed. Use of forbs increased after garbage was no longer readily available. The list of foods we compiled will help managers of grizzly bears and their habitat document future changes in grizzly bear food habits and how bears respond to changing food resources.

Idaho, Montana, Wyoming↗

USGS2005

Estimating site occupancy and abundance using indirect detection indices

Knowledge of factors influencing animal distribution and abundance is essential in many areas of ecological research, management, and policy-making. Because common methods for modeling and estimating abundance (e.g., capture–recapture, distance sampling) are sometimes not practical for large areas or elusive species, indices are sometimes used as surrogate measures of abundance. We present an extension of the Royle and Nichols (2003) generalization of the MacKenzie et al. (2002) site-occupancy model that incorporates length of the sampling interval into the model for detection probability. As a result, we obtain a modeling framework that shows how useful information can be extracted from a class of index methods we call indirect detection indices (IDIs). Examples of IDIs include scent station, tracking tube, snow track, tracking plate, and hair snare surveys. Our model is maximum likelihood, and it can be used to estimate site occupancy and model factors influencing patterns of occupancy and abundance in space. Under certain circumstances, it can also be used to estimate abundance. We evaluated model properties using Monte Carlo simulations and illustrate the method with tracking tube and scent station data. We believe this model will be a useful tool for determining factors that influence animal distribution and abundance.

Journal of Wildlife Management↗

USGS2004

From the field: Efficacy of detecting Chronic Wasting Disease via sampling hunter-killed white-tailed deer

Surveillance programs for Chronic Wasting Disease (CWD) in free-ranging cervids often use a standard of being able to detect 1% prevalence when determining minimum sample sizes. However, 1% prevalence may represent >10,000 infected animals in a population of 1 million, and most wildlife managers would prefer to detect the presence of CWD when far fewer infected animals exist. We wanted to detect the presence of CWD in white-tailed deer ( Odocoileus virginianus ) in Pennsylvania when the disease was present in only 1 of 21 wildlife management units (WMUs) statewide. We used computer simulation to estimate the probability of detecting CWD based on a sampling design to detect the presence of CWD at 0.1% and 1.0% prevalence (23-76 and 225-762 infected deer, respectively) using tissue samples collected from hunter-killed deer. The probability of detection at 0.1% prevalence was <30% with sample sizes of ???6,000 deer, and the probability of detection at 1.0% prevalence was 46-72% with statewide sample sizes of 2,000-6,000 deer. We believe that testing of hunter-killed deer is an essential part of any surveillance program for CWD, but our results demonstrated the importance of a multifaceted surveillance approach for CWD detection rather than sole reliance on testing hunter-killed deer.

Pennsylvania↗

USGS2010

Activity budgets derived from time-depth recorders in a diving mammal

We describe a method to convert continuously collected time–depth data from archival time–depth recorders (TDRs) into activity budgets for a benthic-foraging marine mammal. We used data from 14 TDRs to estimate activity-specific time budgets in sea otters ( Enhydra lutris ) residing near Cross Sound, southeast Alaska, USA. From the TDRs we constructed a continuous record of behavior for each individual over 39–46 days during summer of 1999. Behaviors were classified as foraging (diving to the bottom), other diving (traveling, grooming, interacting), and nondiving (assumed resting). The overall average activity budget (proportion of 24-hr/d) was 0.37 foraging (8.9 hr/d), 0.11 in other diving (2.6 hr/d), and 0.52 nondiving time (12.5 hr/d). We detected significant differences in activity budgets among individuals and between groups within our sample. Historically, the sea otter population in our study area had been expanding and sequentially reoccupying vacant habitat since their reintroduction to the area in the 1960s, and our study animals resided in 2 adjacent yet distinct locations. Males ( n = 5) and individuals residing in recently occupied habitat ( n = 4) spent 0.28–0.30 of their time foraging (6.7–7.2 hr/d), 0.17–0.18 of their time in other diving behaviors (4.1–4.3 hr/d), and 0.53–0.54 of their time resting (12.7–13.0 hr/d). In contrast, females ( n = 9) and individuals residing in longer occupied habitat ( n = 10) spent 0.40 of their time foraging (9.6 hr/d), 0.08–0.09 of their time in other diving behaviors (1.9–2.2 hr/d), and 0.51–0.52 of their time resting (12.2–12.5 hr/d). Consistent with these differences, sea otters residing in more recently occupied habitat captured more and larger clams ( Saxidomus spp., Protothaca spp., Macoma spp., Mya spp., Clinocardium spp.) and other prey, and intertidal clams were more abundant and larger in this area. We found that TDRs provided data useful for measuring activity time budgets and behavior patterns in a diving mammal over long and continuous time periods. Fortuitous contrasts in time budgets between areas where our study animals resided suggest that activity time budgets estimated from TDRs may be a sensitive indicator of population status, particularly in relation to prey availability.

Journal of Wildlife Management↗

USGS2010

Evaluation of harmonic direction-finding systems for detecting locomotor activity

We conducted a physical simulation experiment to test the efficacy of harmonic direction finding for remotely detecting locomotor activity in animals. The ability to remotely detect movement helps to avoid disturbing natural movement behavior. Remote detection implies that the observer can sense only a change in signal bearing. In our simulated movements, small changes in bearing (<5.7??) were routinely undetectable. Detectability improved progressively with the size of the simulated animal movement. The average (??SD) of reflector tag movements correctly detected for 5 observers was 93.9 ?? 12.8% when the tag was moved ???11.5??; most observers correctly detected tag movements ???20.1??. Given our data, one can assess whether the technique will be effective for detecting movements at an observation distance appropriate for the study organism. We recommend that both habitat and behavior of the organism be taken into consideration when contemplating use of this technique for detecting locomotion.

Journal of Wildlife Management↗

USGS2010

Visual implant elastomer mark retention through metamorphosis in amphibian larvae

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.

Journal of Wildlife Management↗

USGS2010

Revisions of rump fat and body scoring indices for deer, elk, and moose

Because they do not require sacrificing animals, body condition scores (BCS), thickness of rump fat (MAXFAT), and other similar predictors of body fat have advanced estimating nutritional condition of ungulates and their use has proliferated in North America in the last decade. However, initial testing of these predictors was too limited to assess their reliability among diverse habitats, ecotypes, subspecies, and populations across the continent. With data collected from mule deer ( Odocoileus hemionus ), elk ( Cervus elaphus ), and moose ( Alces alces ) during initial model development and data collected subsequently from free-ranging mule deer and elk herds across much of the western United States, we evaluated reliability across a broader range of conditions than were initially available. First, to more rigorously test reliability of the MAXFAT index, we evaluated its robustness across the 3 species, using an allometric scaling function to adjust for differences in animal size. We then evaluated MAXFAT, rump body condition score (rBCS), rLIVINDEX (an arithmetic combination of MAXFAT and rBCS), and our new allometrically scaled rump-fat thickness index using data from 815 free-ranging female Roosevelt and Rocky Mountain elk ( C. e. roosevelti and C. e. nelsoni ) from 19 populations encompassing 4 geographic regions and 250 free-ranging female mule deer from 7 populations and 2 regions. We tested for effects of subspecies, geographic region, and captive versus free-ranging existence. Rump-fat thickness, when scaled allometrically with body mass, was related to ingesta-free body fat over a 38–522-kg range of body mass ( r 2 = 0.87; P < 0.001), indicating the technique is remarkably robust among at least the 3 cervid species of our analysis. However, we found an underscoring bias with the rBCS for elk that had >12% body fat. This bias translated into a difference between subspecies, because Rocky Mountain elk tended to be fatter than Roosevelt elk in our sample. Effects of observer error with the rBCS also existed for mule deer with moderate to high levels of body fat, and deer body size significantly affected accuracy of the MAXFAT predictor. Our analyses confirm robustness of the rump-fat index for these 3 species but highlight the potential for bias due to differences in body size and to observer error with BCS scoring. We present alternative LIVINDEX equations where potential bias from rBCS and bias due to body size are eliminated or reduced. These modifications improve the accuracy of estimating body fat for projects intended to monitor nutritional status of herds or to evaluate nutrition's influence on population demographics.

Journal of Wildlife Diseases↗

USGS1985

The effects of catastrophic ecosystem disturbance: the residual mammals at Mount St. Helens

Individuals that survive the direct effects of community- or ecosystem-level disturbances, i.e., "residuals", can have major roles in determining the rate and pathway of subsequent secondary succession. The explosive eruption of the Mount St. Helens volcano on 19 May 1980 resulted in severe damage to a cast array of animal and plant populations (Edwards and Schwartz, 1981; MacMahon, 1982; Hayward et al., 1982). We apply the term "catastrophic" to this event because of its intensity and the large area (>600 km 2 ) over which successional processes were initiated. We present here the results of surveys for mammals, particularly small mammals (excluding bats), conducted in the Mount St. Helens region during the 40 months following the eruption. Our purpose was to elucidate any patterns in species representation that might exist along a gradient of disturbance "intensity", and thus document which species could potentially influence early plant successional patterns there. We infer whether individuals captured were more likely to have been residuals (or their descendants), or immigrants from areas less affected by the eruption, from consideration of the time span between the eruption and the capture date, the trapping location, and life history data. We also make inferences concerning the animal-environment relationships that led to our survey results, and thereby address the question of the likelihood of other types of disturbance, either natural or anthropogenic, producing similar results. Data concerning survival of Thomomys talpoides , the northern pocket gopher, have been presented elsewhere (Andersen, 1982). Initial results from our studies of the relationships among residual small mammals and plant population dynamics are detailed in MacMahon and Warner (1984), Allen et al. (1984) and Andersen and MacMahon (in press).

Washington↗

USGS1988

Tunnel-construction methods and foraging path of a fossorial herbivore, Geomys bursarius

The fossorial rodent Geomys bursarius excavates tunnels to find and gain access to belowground plant parts. This is a study of how the foraging path of this animal, as denoted by feeding-tunnel systems constructed within experimental gardens, reflects both adaptive behavior and constraints associated with the fossorial lifestyle. The principal method of tunnel construction involves the end-to-end linking of short, linear segments whose directionalities are bimodal, but symmetrically distributed about 0°. The sequence of construction of left- and right-directed segments is random, and segments tend to be equal in length. The resulting tunnel advances, zigzag-fashion, along a single heading. This linearity, and the tendency for branches to be orthogonal to the originating tunnel, are consistent with the search path predicted for a "harvesting animal" (Pyke, 1978) from optimal-foraging theory. A suite of physical and physiological constraints on the burrowing process, however, may be responsible for this geometric pattern. That is, by excavating in the most energy-efficient manner, G. bursarius automatically creates the basic components to an optimal-search path. The general search pattern was not influenced by habitat quality (plant density). Branch origins are located more often than expected at plants, demonstrating area-restricted search, a tactic commonly noted in aboveground foragers. The potential trade-offs between construction methods that minimize energy cost and those that minimize vulnerability to predators are discussed.

Journal of Mammalogy↗

USGS1994

Black bears in Arkansas: Characteristics of a successful translocation

In 1958, the Arkansas Game and Fish Commission began translocating black bears ( Ursus americanus ) from Minnesota to the Interior Highlands (Ozark and Ouachita mountains) of Arkansas where bears had been extirpated early in this century. This project continued for 11 years with little public imput, during which time an estimated 254 bears were released. We estimate there are now >2,500 bears in the Interior Highlands of Arkansas, Missouri, and Oklahoma, making it one of the most successful translocations of a Carnivora. Factors that contributed to the success include use of wild-captured animals, elimination of major factors associated with extirpation, release into prime habitats within the former range, multiple release sites, release of 20–40 animals/year for eight years, and release of mostly males prior to release of mostly females. Studies on two allopatric populations demonstrate that they are now diverging in some demographic characteristics, including litter size, cub survivorship, and adult sex-ratio. Translocation of black bears to the Interior Highlands is successful in terms of numbers of animals, but it will not be truly successful until people accept black bears as part of the regional fauna. To that end, those associated with management and research of bears in Arkansas are now focussing on public education and control of nuisance bears.

Arkansas↗

USGS1998

Analysis of the influence of spatial pattern in habitat selection studies

Design and analysis of wildlife habitat selection studies typically do not assess the effect of spatial pattern on the habitat selection process. Effects of landscape scale pattern on habitat selection cannot be accomplished without replicate study areas, because pattern is a single, albeit multifaceted, attribute of an area. For a single area, however, the influence of pattern-related characteristics, such as shape and edge shared with adjacent patches, can be estimated by using GLIM (McCullough and Neider 1983) procedures to model patch-specific frequency counts of animal use as a function of these parameters. This approach is evaluated and illustrated with simulated breeding-bird counts in a South Carolina study area for which a GIS land cover classification is available. A related technique for evaluating whether movement from patch to patch is selective is developed and illustrated for designs that involve collection of trajectory data from monitored individuals. These designs and analyses are feasible given current GIS and GPS technology. Statistical inferences from habitat selection studies should be interpreted within the context of a range of scales at which animals differentiate between patch attributes.

Journal of Agricultural, Biological, and Environme↗

USGS1997

A monoclonal antibody to inclusion body disease of cranes virus enabling specific immunohistochemistry and competitive ELISA

Inclusion body disease of cranes (IBDC) herpesvirus kills some infected cranes and persists in convalescent animals. To enable further study and rapid identification of carrier animals, we developed a monoclonal antibody (MAb) to IBDC virus and used it in immunohistochemistry and a competitive enzyme-linked immunosorbent assay (ELISA). We used conventional techniques to make murine MAbs directed against IBDC virus purified from infected duck embryo cells. Hybridomas reacting in an ELISA with IBDC virus but not uninfected duck embryo cells were characterized by radioimmunoprecipitation, in situ immunohistochemistry, and competitive ELISA with neutralizing and nonneutralizing crane sera. MAb 2C11 immunoprecipitated 59-, 61-, and 110-kD proteins from IBDC virus-infected but not uninfected cells and stained glutaraldehyde-fixed IBDC virus plaques but not surrounding uninfected duck embryo cells in vitro. Antibody 2C11 did not react with duck embryo cells infected with falcon herpesvirus, psittacine herpesvirus, infectious laryngotracheitis, pigeon herpesvirus, or duck plague virus. A competitive ELISA using antibody 2C11 identified most sera that were positive in the neutralization test. This antibody will be useful in further characterizing IBDC virus, its pathogenesis, and its natural history.

Avian Diseases↗

USGS1980

The comparison of usage and availability measurements for evaluating resource preference

Modern ecological research often involves the comparison of the usage of habitat types or food items to the availability of those resources to the animal. Widely used methods of determining preference from measurements of usage and availability depend critically on the array of components that the researcher, often with a degree of arbitrariness, deems available to the animal. This paper proposes a new method, based on ranks of components by usage and by availability. A virtue of the rank procedure is that it provides comparable results whether a questionable component is included or excluded from consideration. Statistical tests of significance are given for the method. The paper also offers a hierarchical ordering of selection processes. This hierarchy resolves certain inconsistencies among studies of selection and is compatible with the analytic technique offered in this paper.

Ecology↗

USGS1992

Estimating transition probabilities for stage-based population projection matrices using capture-recapture data

In stage—based demography, animals are often categorized into size (or mass) classes, and size—based probabilities of surviving and changing mass classes must be estimated before demographic analyses can be conducted. In this paper, we develop two procedures for the estimation of mass transition probabilities from capture—recapture data. The first approach uses a multistate capture—recapture model that is parameterized directly with the transition probabilities of interest. Maximum likelihood estimates are then obtained numerically using program SURVIV. The second approach involvesa modification of Pollock's robust design. Estimation proceeds by conditioning on animals caught in a particualr class at time i, and then using closed models to estimate the number of these that are alive in other classes at i + 1. Both methods are illustrated by application to meadow vole, Microtus pennsylvanicus, capture—recapture data. The two methods produced reasonable estimates that were similar. Advantages of these two approaches include the directness of estimation, the absence of need for restrictive assumptions about the independence of survival and growth, the testability of assumptions, and the testability of related hypotheses of ecological interest (e.g., the hypothesis of temporal variation in transition probabilities).

Ecology↗

USGS1987

The Husting dilemma: A methodological note

Recently, Gill (1985) discussed the interpretation of capture history data resulting from his own studies on the red-spotted newt, Notophthalmus viridescens , and work by Husting (1965) on spotted salamanders, Ambystoma maculatum. Gill (1985) noted that gaps in capture histories (years in which individuals were not captured, preceded and followed by years in which they were) could result from either of two very different possibilities: (1) failure of the animal to return to the fenced pond to breed (the alternative Husting (1965) favored), or (2) return of the animal to the breeding pond, but failure of the investigator to capture it and detect its presence. The authors agree entirely with Gill (1985) that capture history data such as his or those of Husting (1965) should be analyzed using models that recognize the possibility of 'census error,' and that it is important to try to distinguish between such 'error' and skipped breeding efforts. The purpose of this note is to point out the relationship between Gill's (1985:347) null model and certain capture-recapture models, and to use capture-recapture models and tests to analyze the original data of Husting (1965).

Ecology↗

USGS1987

Geomys bursars burrowing patterns: influence of season and food patch structure

The relationship between belowground food resources and the pattern and pace of soil excavation by Geomys bursarius, the plains pocket gopher, was assessed during spring and autumn using replicated 18 x 18 m enclosures containing uniform arrays of food plants (Daucus carota) at spacings assumed to result in burrowing being energetically profitable (25 and 50 cm) or unprofitable (100 cm and empty). Soil excavation rate, measured in terms of either daily additions to tunnel length or volume, or the maximum volume excavated during a 3—d interval, varied greatly among individuals. No significant effect due to season or density of belowground plant biomass was detected when burrowing was profitable. Individuals readily initiated aboveground travel in unprofitable treatments. Soil bulk density was negatively related and animal body mass positively related to excavation rate. Individuals deposited from 41 to 87% of excavated soil on the ground surface; the remainder was used to backfill previously created tunnels or chambers. Plant size, but not plant spacing, affected the ratio of the volumes deposited aboveground and belowground. There was no evidence that animals in enclosures disturbed soil in a manner quantitatively or qualitatively different from free—ranging adults. The large proportions and absolute quantities (up to 30 L/d) of soil involved suggest that backfilling may affect ecosystem structure and functioning as much as surface mound—building.

Ecology↗

USGS1996

Assessing habitat selection when availability changes

We present a method of comparing data on habitat use and availability that allows availability to differ among observations. This method is applicable when habitats change over time and when animals are unable to move throughout a predetermined study area between observations. We used maximum—likelihood techniques to derive an index that estimates the probability that each habitat type would be used if all were equally available. We also demonstrate how these indices can be used to compare relative use of available habitats, assign them ranks, and assess statistical differences between pairs of indices. The set of these indices for all habitats can be compared between groups of animals that represent different seasons, sex or age classes, or experimental treatments. This method allows quantitative comparisons among types and is not affected by arbitrary decisions about which habitats to include in the study. We provide an example by comparing the availability of four categories of sea ice concentration to their use by adult female polar bears (Ursus maritimus), whose movements were monitored by satellite radio tracking in the Bering and Chukchi Seas during 1990. Use of ice categories by bears was nonrandom, and the pattern of use differed between spring and late summer seasons.

Ecology↗

USGS1976

The abundance and diversity of the herpetofaunas of tropical forest litters

Quantitative and qualitative samples of amphibian and lizard faunas were taken from forest litter in Costa Rica and compared with similar samples collected in Borneo, the Philippines, and Panama. Animal abundance is about ten times greater in Costa Rican lowland wet forest than in Borneo. Radically different routes and rates of energy flow are postulated to account for the difference. In a series of upland (1010-1425 m) samples in the Philippines, the number of litter lizards and frogs increases with elevation. A single upland (1200 m) Costa Rican sample contains about three times as many animals per 100 m2 as two lowland sites. This increase with altitude correlates well with hypotheses that overall tropical forest productivity is greatest at intermediate elevations. Herpetofaunal densities are greater in wet areas compared to dry sites and flat terrain compared to slopes. These observations are linked to the greater variation and lesser total litter fall in dry sites and/or slopes. The number of species of amphibians and lizards regularly inhabiting the litter is similar in all wet lowland forests studied. Increasing elevation and decreasing rainfall correlate with faunas having fewer species. The former is seen as the result of the differential ability of lowland species to invade uplands, and the latter as a decrease in the kind and duration of frog-spawning sites. Reduced equitability with increasing elevation is principally due to the much greater proportional increase of the commonest species. In the evolution of American and Bornean-Philippine wet lowland faunas, frogs with direct development (Eleutherodactylus) have radiated in the former in the same fashion that skinks have in the latter.

Biotropica↗