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At least 1,153 records · Page 64Linked to original sources

Evaluation of age determination techniques for gray wolves

We evaluated tooth wear, cranial suture fusion, closure of the canine pulp cavity, and cementum annuli as methods of age determination for known- and unknown-age gray wolves (Canis lupus) from Alaska, Minnesota, Ontario, and Isle Royale, Michigan. We developed age classes for cranial suture closure and tooth wear. We used measurement data obtained from known-age captive and wild wolves to generate a regression equation to predict age based on the degree of closure of the canine pulp cavity. Cementum annuli were studied in known- and unknown-age animals, and calcified, unstained thin sections were found to provide clear annulus patterns under polarized transmitted light. Annuli counts varied among observers, partly because of variation in the pattern of annuli in different regions of the cementum. This variation emphasizes the need for standardized models of cementum analysis. Cranial suture fusion is of limited utility in age determination, while tooth wear can be used to estimate age of adult wolves within 4 years. Wolves <7 years old could be aged to within 1-3 years with the regression equation for closure of the canine pulp cavity. Although inaccuracy remains a problem, cementum-annulus counts were the most promising means of estimating age for gray wolves.

Journal of Wildlife Management↗

Estimating survival rates with age-structure data

We developed a general statistical model that provides a comprehensive framework for inference about survival rates based on standing age-structure and ages-at-death data. Previously available estimators are maximum likelihood under the general model, but they use only 1 type of data and require the assumption of a stable age structure and a known population growth rate. We used the general model to derive new survival rate estimators that use both types of data and require only the assumption of a stable age structure or a known population growth rate. Our likelihood-based approach allows use of standard model-selection procedures to test hypotheses about age-structure stability, population growth rates, and age-related patterns in survival. We used this approach to estimate survival rates for female sea otters ( Enhydra lutris ) in Prince William Sound, Alaska.

Journal of Wildlife Management↗

Limits of retrospective power analysis

Power analysis after study completion has been suggested to interpret study results. We present 3 methods of estimating power and discuss their limitations. We use simulation studies to show that estimated power can be biased, extremely variable, and severely bounded. We endorse the practice of computing power to detect a biologically meaningful difference as a tool for study planning but suggest that calculation of confidence intervals on the parameter of interest is the appropriate way to gauge the strength and biological meaning of study results.

Journal of Wildlife Management↗

Survival and recovery rates of American eiders in eastern North America

We analyzed banding and recovery data of adult female American eiders ( Somateria mollissima dresseri ) captured during the breeding season in eastern North America. We estimated survival rates for birds originating in the Atlantic Coast subpopulation to be 0.8730 ± 0.0156 (SE) while recovery rates were 0.0101 ± 0.0080 (SE). Support for several banding reference areas of American eiders was found. No trends were detected in band recovery, harvest rates or harvest over time.

Journal of Wildlife Management↗

Distribution of black-tailed jackrabbit habitat determined by GIS in southwestern Idaho

We developed a multivariate description of black-tailed jackrabbit (Lepus californicus) habitat associations from Geographical Information Systems (GIS) signatures surrounding known jackrabbit locations in the Snake River Birds of Prey National Conservation Area (NCA), in southwestern Idaho. Habitat associations were determined for characteristics within a 1-km radius (approx home range size) of jackrabbits sighted on night spotlight surveys conducted from 1987 through 1995. Predictive habitat variables were number of shrub, agriculture, and hydrography cells, mean and standard deviation of shrub patch size, habitat richness, and a measure of spatial heterogeneity. In winter, jackrabbits used smaller and less variable sizes of shrub patches and areas of higher spatial heterogeneity when compared to summer observations (P < 0.05). During the low population phase, jackrabbits also used agricultural regions more during winter than summer. The association with agricultural regions was emphasized spatially in a GIS map contrasting winter and summer periods. Multivariate habitat means (P < 0.001), but not individual GIS variables (P > 0.05), differed significantly between high and low population phase. We used the Mahalanobis distance statistic to rank all 50-m cells in a 440,000-ha region relative to the multivariate mean habitat vector. On verification surveys to test predicted models, we sighted jackrabbits in areas ranked close to the mean habitat vector. Areas burned by large-scale fires between 1980 and 1992 or in an area repeatedly burned by military training activities had greater Mahalanobis distances from the mean habitat vector than unburned areas and were less likely to contain habitats used by jackrabbits.

Journal of Wildlife Management↗

Use of burrow entrances to indicate densities of Townsend's ground squirrels

Counts of burrow entrances have been positively correlated with densities of semi-fossorial rodents and used as an index of densities. We evaluated their effectiveness in indexing densities of Townsend's ground squirrels ( Spermophilus townsendii ) in the Snake River Birds of Prey National Conservation Area (SRBOPNCA), Idaho, by comparing burrow entrance densities to densities of ground squirrels estimated from livetrapping in 2 consecutive years over which squirrel populations declined by >75%. We did not detect a consistent relation between burrow entrance counts and ground squirrel density estimates within or among habitat types. Scatter plots indicated that burrow entrances had little predictive power at intermediate densities. Burrow entrance counts did not reflect the magnitude of a between-year density decline. Repeated counts of entrances late in the squirrels' active season varied in a manner that would be difficult to use for calibration of transects sampled only once during this period. Annual persistence of burrow entrances varied between habitats. Trained observers were inconsistent in assigning active-inactive status to entrances. We recommend that burrow entrance counts not be used as measures or indices of ground squirrel densities in shrubsteppe habitats, and that the method be verified thoroughly before being used in other habitats.

Idaho↗

Survival of spectacled eider adult females and ducklings during brood rearing

We studied survival of adult female and duckling spectacled eiders ( Somateria fischeri ) during brood rearing on the Yukon-Kuskokwim Delta, Alaska from 1993 to 1995. Duckling survival to 30 days of age averaged 34% with a 95% confidence interval from 25 to 47%. Half (49%) of radiomarked adult females had lost all their ducklings by 30 days after hatch. Most (74%) duckling mortality occurred in the first 10 days. Adult female survival during the first 30 days of brood rearing was 93 ± 3% (SE). Females died from lead poisoning, as a result of ingesting lead shot, and predation. Mortality of adult females during brood rearing is probably higher than during other times of the year. Low adult female survival during the breeding season may be contributing to the overall population decline of spectacled eiders.

Alaska↗

Population dynamics of white-winged scoters

A significant ( P < 0.01) decline between 1961 and 1993 in ratio of harvested young per adult in the Atlantic Flyway (age ration) of white-winged scoters ( Melanitta fusca ) led us to examine annual survival rates and harvest of this species. Compared to waterfowl with similar life histories, black scoters ( M. nigra ) and surf scoters ( M. perspicillata ), the decline in age ratios of white-winged scoter age ratios was not significantly different ( P = 0.11). Adult females banded at Redberry Lake, Saskatchewan that winter along both coasts, had high annual survival rates (0.773 ± 0.0176 [SE]). High harvest in the Atlantic Flyway was not followed by an increase in production (age ratios) the following year or 2, i.e., there was no short-term rebound in recruitment by the population. Harvest of white-winged scoters in the Atlantic Flyway was explained by the age ratio in the fall flight and by hunter effort.

Connecticut, Delaware, Maryland, Massachusetts, Ne↗

Site-specific lead exposure from lead pellet ingestion in sentinel mallards

We monitored lead poisoning from the ingestion of spent lead pellets in sentinel mallards (Anas platyhrynchos) at the Sacramento National Wildlife Refuge (SNWR), Willows, California for 4 years (1986-89) after the conversion to steel shot for waterfowl hunting on refuges in 1986. Sentinel mallards were held in 1.6-ha enclosures in 1 hunted (P8) and 2 non-hunted (T19 and TF) wetlands. We compared site-specific rates of lead exposure, as determined by periodic measurement of blood lead concentrations, and lead poisoning mortality between wetlands with different lead pellet densities, between seasons, and between male and female sentinels. In 1986, the estimated 2-week rate of lead exposure was significantly higher (P < 0.005) in P8 (43.8%), the wetland with the highest density of spent lead pellets (>2,000,000 pellets/ha), than in those with lower densities of lead pellets, T19 (18.1%; 173,200 pellets/ha) and TF (0.9%; 15,750 pellets/ha). The probability of mortality from lead poisoning was also significantly higher (P < 0.01) in sentinel mallards enclosed in P8 (0.25) than T19 (0) and TF (0) in 1986 and remained significantly higher (P < 0.001) during the 4-year study. Both lead exposure and the probability of lead poisoning mortality in P8 were significantly higher (P < 0.001) in the fall of 1986 (43.8%; 0.25), before hunting season, than in the spring of 1987 (21.6%; 0.04), after hunting season. We found no significant differences in the rates of lead exposure or lead poisoning mortality between male and female sentinel mallards. The results of this study demonstrate that in some locations, lead exposure and lead poisoning in waterfowl will continue to occur despite the conversion to steel shot for waterfowl hunting.

California↗

Survival of juvenile black brant during brood rearing

Survival of young is an important and poorly understood component of waterfowl productivity. We estimated survival of black brant ( Branta bernicla nigricans ) goslings during summers 1987-89 on the Yukon-Kuskokwim Delta, Alaska, to determine timing and magnitude of gosling mortality and to compare methods of estimating gosling survival. Eighty-two percent of radio-tagged adult females (n = 61) fledged ≥1 gosling (brood success). We estimated survival of goslings within broods by 3 methods: (1) changes in mean brood size through time, (2) observation of goslings associated with marked adults, and (3) age ratios of brant captured in banding drives. Estimates of gosling survival within successful broods averaged 81% and ranged from 66 to 92%. Combining brood success and gosling survival within successful broods yielded estimates of overall gosling survival that averaged 68%, ranging from 79% in 1987 to 56% in 1989. Eighty-two percent of gosling mortality occurred in the first 15 days. Estimates of survival on the basis of age ratios of birds captured in banding drives are biased low. Our estimates of average gosling survival are higher than reported for other species of geese.

Alaska↗

Factors affecting visibility rate of aerial waterfowl surveys in the Mississippi alluvial valley

Because visibility bias can confound attempts to detect changes in abundance, we evaluated factors that affect visibility rate in aerial surveys of wintering waterfowl. We placed waterfowl decoys in 32 2- x 0.25-km strip transects in the Mississippi Alluvial Valley (MAV) during February 1990 and 1991 and observed the decoys under different experimental conditions. Visibility rate was influenced ( P < 0.10) by habitat, transect width, and decoy group size. We simulated variation in use of habitat and found that changes in use between open and wooded wetlands would cause changes in visibility rate and affect the power to detect a change in abundance. The effect of changes in visibility rate on likelihood of detecting population change depended on the magnitude and direction of population change and precision of the population index. For transect surveys of wintering ducks in the MAV we recommend reducing transect width from 250 to 150 m on each side of the aircraft and restricting comparisons between years when 70% of the population is likely to be distributed in open wetlands. Improved techniques for estimating abundance of wintering waterfowl are also needed so use of questionable population indices can be avoided.

Mississippi↗

Effects of canine parvovirus on gray wolves in Minnesota

Long-term effects of disease on wild animal population demography is not well documented. We studied a gray wolf (Canis lupus) population in a 2,060-km 2 area of Minnesota for 15 years to determine its response to canine parvovirus (CPV). The CPV had little effect ( P > 0.05) on wolf population size while epizootic during 1979-83. However, after CPV became enzootic, percentage of pups captured during summer-fall 1984-93 and changes in subsequent winter wolf numbers were each inversely related to the serological prevalence of CPV in wolves captured during July-November ( r 2 = 0.39 and 0.72, P = 0.05 and < 0.01, respectively). The CPV antibody prevalence in adult wolves increased to 87% in 1993 (r2 = 0.28, P = 0.05). However, because population level remained stable, CPV-induced mortality appeared to compensate for other mortality factors such as starvation. We -predict that the winter wolf population will decline when CPV prevalence in adults consistently exceeds 76%. The CPV may become important in limiting wolf populations.

Minnesota↗

Caribou calf mortality in Denali National Park, Alaska

Calf mortality is a major component of caribou (Rangifer tarandus) population dynamics, but little is known about the timing or causes of calf losses, or of characteristics that predispose calves to mortality. During 1984-87, we radiocollared 226 calves (≤3 days old) in the Denali Caribou Herd (DCH), an unhunted population utilized by a natural complement of predators, to determine the extent, timing, and causes of calf mortality and to evaluate influences of year, sex, birthdate, and birth mass on those losses. Overall, 39% of radio-collared calves died as neonates (≤15 days old), and 98% of those deaths were attributed to predation. Most neonatal deaths (85%) occurred within 8 days of birth. Few deaths occurred after the neonatal period (5, 10, and 0% of calves instrumented died during 16-30, 31-150, and >150 days of age, respectively). Survival of neonates was lower (P = 0.038) in 1985, following a severe winter, than during the other 3 years. In years other than 1985, calves born during the peak of calving (approx 50% of the total, born 5-8 days after calving onset) experienced higher (P < 0.001) neonatal survival than did other calves. Grizzly bears (Ursus arctos), wolves (Canis lupus), and unknown large predators (i.e., grizzly bears or wolves) accounted for 49, 29, and 16% of the neonatal deaths, respectively. The rate of bear-caused mortalities declined (P < 0.001) with calf age, and bears killed few calves >10 days old. Wolf predation was not related (P > 0.05) to calf age and peaked 10 days after onset of calving. Grizzly bear and wolf predation on neonates during the calving season was a limiting factor for the Denali Caribou Herd.

Journal of Wildlife Management↗

Use of solicited bands and separation of hunting and natural mortality: a comment

We previously presented (Conroy 1985, Conroy et al. 1989) models for analysis of band recovery data stratified into those voluntarily reported and those obtained by solicitation, similar to models described by Pollock et al. (1994). We discuss differences between the 2 modeling approaches and suggest designs and analyses involving overlapping samples of standard and reward bands to enable adjustment for temporal and geographic variation in reporting and solicitation rates,

Journal of Wildlife Management↗

An aerial sightability model for estimating ferruginous hawk population size

Most raptor aerial survey projects have focused on numeric description of visibility bias without identifying the contributing factors or developing predictive models to account for imperfect detection rates. Our goal was to develop a sightability model for nesting ferruginous hawks (Buteo regalis) that could account for nests missed during aerial surveys and provide more accurate population estimates. Eighteen observers, all unfamiliar with nest locations in a known population, searched for nests within 300 m of flight transects via a Maule fixed-wing aircraft. Flight variables tested for their influence on nest-detection rates included aircraft speed, height, direction of travel, time of day, light condition, distance to nest, and observer experience level. Nest variables included status (active vs. inactive), condition (i.e., excellent, good, fair, poor, bad), substrate type, topography, and tree density. A multiple logistic regression model identified nest substrate type, distance to nest, and observer experience level as significant predictors of detection rates (P < 0.05). The overall model was significant (??26 = 124.4, P < 0.001, n = 255 nest observations), and the correct classification rate was 78.4%. During 2 validation surveys, observers saw 23.7% (14/59) and 36.5% (23/63) of the actual population. Sightability model predictions, with 90% confidence intervals, captured the true population in both tests. Our results indicate standardized aerial surveys, when used in conjunction with the predictive sightability model, can provide unbiased population estimates for nesting ferruginous hawks.

Journal of Wildlife Management↗

The effectiveness of tape playbacks in estimating Black Rail densities

Tape playback is often the only efficient technique to survey for secretive birds. We measured the vocal responses and movements of radio-tagged black rails (Laterallus jamaicensis; 26 M, 17 F) to playback of vocalizations at 2 sites in Florida during the breeding seasons of 1992-95. We used coefficients from logistic regression equations to model probability of a response conditional to the birds' sex. nesting status, distance to playback source, and time of survey. With a probability of 0.811, nonnesting male black rails were ))lost likely to respond to playback, while nesting females were the least likely to respond (probability = 0.189). We used linear regression to determine daily, monthly and annual variation in response from weekly playback surveys along a fixed route during the breeding seasons of 1993-95. Significant sources of variation in the regression model were month (F3.48 = 3.89, P = 0.014), year (F2.48 = 9.37, P < 0.001), temperature (F1.48 = 5.44, P = 0.024), and month X year (F5.48 = 2.69, P = 0.031). The model was highly significant (P < 0.001) and explained 54% of the variation of mean response per survey period (r2 = 0.54). We combined response probability data from radiotagged black rails with playback survey route data to provide a density estimate of 0.25 birds/ha for the St. Johns National Wildlife Refuge. The relation between the number of black rails heard during playback surveys to the actual number present was influenced by a number of variables. We recommend caution when making density estimates from tape playback surveys

Journal of Wildlife Management↗