SEARCH · USGS Science

Results for “Wildlife Disease”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

SourceResearch connectionFrom yearThrough year

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

1,304 records · Page 73Linked to original sources

USGS1989

Population ecology and harvest of the American black duck: a review

1. The purpose of our review was to examine available data on population trends and current status of black ducks and trends in natality and survival and to relate these, where possible, to changes in habitat, predation, disease, contaminants, harvest, and hybridization with mallards. 2. The number of black ducks tallied in the winter survey has declined steadily over the past 30 years at an average rate of about 3%/ year. Reliability and precision of the survey are uncertain; it may not provide an adequate index to the continental population of black ducks. Breeding surveys are incomplete and sporadic, but black ducks have decreased in Ontario and increased in the Maritime Provinces and Quebec. 3. Recent declines in numbers of black ducks tallied in the winter survey are not unusual in magnitude or much different from those that have occurred among several other species of waterfowl. 4. At present, black ducks are not especially scarce relative to numbers of several other ducks in eastern North America. 5. There is no solid evidence of major decreases in quality or quantity of breeding habitat for black ducks in recent years; in some areas, habitat has improved. 6. Natural mortality of black ducks has not been well studied, but does not seem unusually high compared to other dabbling ducks. 7. Harvest rates of black ducks are similar to those of sympatric mallards as determined by banding analyses. 8. There is no strong evidence for direct effects of contaminants on black ducks, but some indirect effects through invertebrate food resources have been detected. 9. Age ratios in black ducks show no trend in the past 18 years. 10. The quality and quantity of wintering habitat for black ducks have decreased substantially in some areas. 11. Disease and other natural mortality that affect black ducks do .not occur in unusually high frequency. 12. A decline in harvest of black ducks has occurred; most of the decline has been in the United States, especially since restrictive regulations were implemented in 1983. 13. Recovery rates of black ducks have declined recently in the U.S., but not in Canada. 14. Survival rates of black ducks are 56-63% for adults and 43% for young. These rates of survival are similar to comparable estimates in sympatric mallards. 15. Long hunting seasons may depress survival in some sex-age classes of black ducks, buteffects of small reductions in survival on population trends are unknown. 16. Available evidence does not support the contention that hunting is either the sole or most important cause of the decline in the winter tally of black duck numbers. 17. Surveys and banding of black ducks should be thoroughly reviewed and maintained or improved as warranted. Obtaining or maintaining a reasonable index to numbers of black ducks is the top priority among survey needs. 18. Experimental manipulation of hunting seasons should be considered to elucidate relationships among regulations, harvest, survival, and population trends. 19. Black ducks and mallards are genetically similar; there is as much genetic differentiation within the 2 species as there is between them. 20. Black duck x mallard hybrids are fertile. Hybrids are difficult to detect by plumage and thus published frequencies (0-13%) of hybrids may be low. 21. Hybridization could be a result of concomitant mallard increases and black duck decreases, or changes in black duck-to-mallard ratios could be from hybridization and genetic swamping of black ducks.

Wildlife Society Bulletin↗

USGS1995

Spring-staging ecology of midcontinent greater white-fronted geese

A major part of the midcontinent greater white-fronted goose ( Anser albifrons ) population stages for several weeks in spring in the Rainwater Basin Area (RBA) of south-central Nebraska where substantial mortality from disease occurs periodically. Effective management of this population requires better data on use of habitat, vulnerability to disease, and the role of staging areas in migration and reproduction. We studied use of habitat, foods, nutrient dynamics, and effect of changes in agriculture on food availability and habitat needs in spring 1979-80. During daylight, geese were observed primarily in harvested cornfields (76%) and growing winter wheat (23%). Corn grain and winter wheat shoots composed 90 and 9%, respectively, of foods consumed by collected geese ( n = 42). Feeding activity did not vary among post-harvest cornfield treatments except that little feeding occurred ( P < 0.05) in moldboard-plowed fields (<1%). Fat content for all geese increased ( P ≤ 0.01) with Julian date; protein content increased ( P = 0.03) only among adult females, and there was no evidence ( P > 0.05) of temporal variation in calcium content. Adult geese storing 14.2 g of fat per day deposited approximately 582 g of fat between 22 February and 8 April. Energy requirements for thermal regulation were small compared with requirements for fat synthesis and probably had little effect on nutrient deposition. The 34,000 white-fronted geese present on the Harvard Marsh and Prairie Dog Marsh study areas in March 1980 probably used <20% of the corn available within a 5-km radius. We believe that midcontinent white-fronted geese arrive on Arctic breeding grounds with larger and less variable fat reserves than prior to modern agricultural development. We attribute this response to increased food availability on staging areas where the net effect of agricultural changes has been an increase in corn availability. Waterfowl managers can increase dispersion of geese and provide favorable foraging conditions by maintaining well-distributed wetland roosting habitat and by working with private landowners to ensure access to grain in the vicinity of wetlands.

Nebraska↗

USGS2025

Trophic transfer of fipronil residues to black-footed ferrets: Implications for ferret safety, flea control, and plague mitigation

Sylvatic plague, caused by the flea-borne bacterium Yersinia pestis , is an invasive disease in North America that causes reductions of native fauna and transforms ecosystems. Fipronil baits have shown promise in reducing flea loads on prairie dogs Cynomys spp. for plague mitigation. Many species depend on prairie dogs and their ecological influences, including the black-footed ferret Mustela nigripes (ferret), an obligate predator of prairie dogs. To better understand how fipronil affects ferrets, we offered carcass portions from black-tailed prairie dogs C. ludovicianus that had consumed fipronil bait (0.005% fipronil by weight) to captive ferrets and monitored their health. We fed carcass portions of three prairie dogs to four adult ferrets for 1 week. No ill effects were observed in the ferrets. We collected scat from the ferrets before, during, and after their feeding on treated prairie dogs. We evaluated potential effects of ferret scat on larval fleas, which feed on organic matter. Fipronil residues were not detected in ferret scat samples collected before treatment. During and shortly after treatment, ferret scat contained 3.76 ng/g fipronil and 13.75 ng/g fipronil sulfone, on average, demonstrating trophic transfer of the residues from prey to predator. We presented 0.5 mg of ferret scat to each of 96 larval Oropsylla montana (Siphonaptera: Ceratophyllidae) and assessed survival rates over 24 h. When exposed to ferret scat lacking fipronil residues, 85% of larvae survived. Survival was reduced to 61% and 35% for larvae contacting or consuming scat with fipronil-residue, respectively. Fipronil residues in scat from a variety of species on prairie dog colonies, perhaps especially the prairie dogs, may assist in flea control and plague mitigation. Hosts eliminate fipronil residues, and fipronil residues in the environment degrade over time, reducing but not eliminating potential concerns with bioaccumulation.

Journal of Fish and Wildlife Management↗

USGS2025

White‐tailed deer habitat use and implications for chronic wasting disease transmission

Animal space use, activity patterns, and habitat selection—and heterogeneity in these patterns—have important implications for where and when infectious diseases are transmitted. White-tailed deer ( Odocoileus virginianus ) are habitat generalists, with a high degree of heterogeneity in their movement ecology based on sex, age, season, and region. These heterogeneities have important implications for the transmission and management of chronic wasting disease (CWD), which is a deadly prion disease transmitted both directly and indirectly through the environment. As such, favored deer habitats may promote direct interactions between conspecifics or indirect spatial overlap and subsequent environmental transmission. However, little is known about how individual animal space use translates to actual spatial overlap between individuals, leaving uncertainty in how habitat shapes the risk of direct or environmental CWD transmission. In this study, we evaluated seasonal activity patterns, home ranges, and habitat selection for 596 white-tailed deer in southwest Wisconsin, USA, from 2017-2022. We also estimated seasonal encounter distributions—regions where a pair of deer were most likely to encounter each other—for all pairs of deer putatively in different social groups (between-group) in our study, and quantified seasonal variation in the habitat composition of these areas. We found that deer selection for crops, pasture, or grasslands was generally low, relative to forest, but was highest in the post-fawning (summer) and non-breeding (winter) seasons. We observed similar patterns for the habitat composition of encounter distributions, suggesting that crops, pasture, and grasslands may be attractive resources that facilitate between-group transmission. Site fidelity between years was generally high; combined with small female home ranges in the fawning season, this implies that females likely re-use the same small, high-quality fawning habitats from year to year. We found that attraction toward between-group individuals was low during the post-fawning season but high during the breeding (fall) and non-breeding seasons. These results suggest that space use and habitat selection could shape the risk of environmental transmission in the fawning and post-fawning seasons, social selection could favor direct transmission risk in the breeding season, and combined social and habitat selection may shape risk of both direct and environmental transmission during the non-breeding season. We provide a detailed picture of the physiological and social drivers of deer movement through the year, with implications for CWD transmission and management.

Iowa, Wisconsin↗

USGS2017

Paltry past-precipitation: Predisposing prairie dogs to plague?

The plague bacterium Yersinia pestis was introduced to California in 1900 and spread rapidly as a sylvatic disease of mammalian hosts and flea vectors, invading the Great Plains in the United States by the 1930s to 1940s. In grassland ecosystems, plague causes periodic, devastating epizootics in colonies of black-tailed prairie dogs ( Cynomys ludovicianus ), sciurid rodents that create and maintain subterranean burrows. In doing so, plague inhibits prairie dogs from functioning as keystone species of grassland communities. The rate at which fleas transmit Y. pestis is thought to increase when fleas are abundant. Flea densities can increase during droughts when vegetative production is reduced and herbivorous prairie dogs are malnourished and have weakened defenses against fleas. Epizootics of plague have erupted frequently in prairie dogs during years in which precipitation was plentiful, and the accompanying cool temperatures might have facilitated the rate at which fleas transmitted Y. pestis . Together these observations evoke the hypothesis that transitions from dry-to-wet years provide conditions for plague epizootics in prairie dogs. Using generalized linear models, we analyzed a 24-year dataset on the occurrence of plague epizootics in 42 colonies of prairie dogs from Colorado, USA, 1982–2005. Of the 33 epizootics observed, 52% erupted during years with increased precipitation in summer. For the years with increased summer precipitation, if precipitation in the prior growing season declined from the maximum of 502 mm to the minimum of 200 mm, the prevalence of plague epizootics was predicted to increase 3-fold. Thus, reduced precipitation may have predisposed prairie dogs to plague epizootics when moisture returned. Biologists sometimes assume dry conditions are detrimental for plague. However, 48% of epizootics occurred during years in which precipitation was scarce in summer. In some cases, an increased abundance of fleas during dry years might compensate for other conditions that become less favorable for plague transmission. Global warming is forecasted to amplify the hydrological cycle in the Great Plains, causing an increased occurrence of prolonged droughts interceded by brief periods of intense precipitation. Results herein suggest these changes might affect plague cycles in prairie dogs. Both negative and positive consequences of dry conditions should be considered when managing plague.

Journal of Wildlife Management↗

USGS2015

Estimating the phenology of elk brucellosis transmission with hierarchical models of cause-specific and baseline hazards

Understanding the seasonal timing of disease transmission can lead to more effective control strategies, but the seasonality of transmission is often unknown for pathogens transmitted directly. We inserted vaginal implant transmitters (VITs) in 575 elk ( Cervus elaphus canadensis ) from 2006 to 2014 to assess when reproductive failures (i.e., abortions or still births) occur, which is the primary transmission route of Brucella abortus , the causative agent of brucellosis in the Greater Yellowstone Ecosystem. Using a survival analysis framework, we developed a Bayesian hierarchical model that simultaneously estimated the total baseline hazard of a reproductive event as well as its 2 mutually exclusive parts (abortions or live births). Approximately, 16% (95% CI = 0.10, 0.23) of the pregnant seropositive elk had reproductive failures, whereas 2% (95% CI = 0.01, 0.04) of the seronegative elk had probable abortions. Reproductive failures could have occurred as early as 13 February and as late as 10 July, peaking from March through May. Model results suggest that less than 5% of likely abortions occurred after 6 June each year and abortions were approximately 5 times more likely in March, April, or May compared to February or June. In western Wyoming, supplemental feeding of elk begins in December and ends during the peak of elk abortions and brucellosis transmission (i.e., Mar and Apr). Years with more snow may enhance elk-to-elk transmission on supplemental feeding areas because elk are artificially aggregated for the majority of the transmission season. Elk-to-cattle transmission will depend on the transmission period relative to the end of the supplemental feeding season, elk seroprevalence, population size, and the amount of commingling. Our statistical approach allowed us to estimate the probability density function of different event types over time, which may be applicable to other cause-specific survival analyses. It is often challenging to assess the cause of death, or in this case whether the reproductive event was an abortion or live birth. Accounting for uncertainty in the event type is an important future addition to our methodological approach.

Wyoming↗

USGS2015

Modeling risk of pneumonia epizootics in bighorn sheep

Pneumonia epizootics are a major challenge for management of bighorn sheep ( Ovis canadensis ) affecting persistence of herds, satisfaction of stakeholders, and allocations of resources by management agencies. Risk factors associated with the disease are poorly understood, making pneumonia epizootics hard to predict; such epizootics are thus managed reactively rather than proactively. We developed a model for herds in Montana that identifies risk factors and addresses biological questions about risk. Using Bayesian logistic regression with repeated measures, we found that private land, weed control using domestic sheep or goats, pneumonia history, and herd density were positively associated with risk of pneumonia epizootics in 43 herds that experienced 22 epizootics out of 637 herd-years from 1979–2013. We defined an area of high risk for pathogen exposure as the area of each herd distribution plus a 14.5-km buffer from that boundary. Within this area, the odds of a pneumonia epizootic increased by >1.5 times per additional unit of private land (unit is the standardized % of private land where global  = 25.58% and SD = 14.53%). Odds were >3.3 times greater if domestic sheep or goats were used for weed control in a herd's area of high risk. If a herd or its neighbors within the area of high risk had a history of a pneumonia epizootic, odds of a subsequent pneumonia epizootic were >10 times greater. Risk greatly increased when herds were at high density, with nearly 15 times greater odds of a pneumonia epizootic compared to when herds were at low density. Odds of a pneumonia epizootic also appeared to decrease following increased spring precipitation (odds = 0.41 per unit increase, global  = 100.18% and SD = 26.97%). Risk was not associated with number of federal sheep and goat allotments, proximity to nearest herds of bighorn sheep, ratio of rams to ewes, percentage of average winter precipitation, or whether herds were of native versus mixed or reintroduced origin. We conclude that factors associated with risk of pneumonia epizootics are complex and may not always be from the most obvious sources. The ability to identify high-risk herds will help biologists and managers determine where to focus management efforts and the risk factors that most affect each herd, facilitating more effective, proactive management.

Journal of Wildlife Management↗

USGS2007

Determining the pattern of cementum annuli and relationship to reproduction in male sea otters

Since the early 1990s, the southwestern Alaskan sea otter (Enhydra lutris) population has declined dramatically and the cause has yet to be determined. Population trajectories of large mammals are determined by three factors: survival rate, reproduction rate, and age of first reproduction (AFR). Of these three, AFR should respond first to environmental change. Life history theory predicts that AFR will be older with bottom-up causes (ie, food limitation) and younger when the cause of the decline is top-down (ie, predation), as there is usually abundant resources in this scenario. Traditionally, determining AFR required lethal sampling, which may not always be possible. Work on many mammalian species suggests that the width of annual cementum layers in teeth may decline when breeding begins. If so, examining teeth annuli may provide a nonlethal alternative for determining AFR. Ongoing research has shown this relationship in female sea otters, but male sea otters have not been tested. Sea otter testes and premolar teeth slides were collected by subsistence hunters working with the US Fish and Wildlife Service and the Alaska Sea Otter and Steller Sea Lion Commission from Alaska (1994– 2005). We determined the pattern in cementum annuli thickness for male sea otters across age by measuring annuli at three sites on each of the two slide sections available. We found that cementum annuli layers decreased with age, but found no correlation between cementum annuli and sexual maturity in male sea otters. This lack of correlation may be due to sampling error or different energy expenditures during reproduction for each sex. Since females expend large amounts of energy through gestation and lactation, we hypothesize that the width of female cementum annuli decreases at a much sharper rate when they reach AFR. The southwest Alaskan sea otter population has plummeted up to 90% since the early 1990s and the reason is unknown.1 Declines may be due to a bottom-up source caused by lack of food and habitat that occurs when populations are dense, in which case we would expect reproduction rates to decrease and age of first reproduction (AFR) to increase. However, circumstantial evidence suggests that the decline may be due to a top-down source, ie, predation.2 In this case, we would expect reproduction rates to increase and AFR to decrease due to lowered densities that coincide with top-down declines.3 An ongoing study of female sea otters has shown that past reproduction can be determined by analysis of cementum annuli in the teeth, and used to calculate AFR.4 Cementum annuli are annual deposits of minerals that occur on the root of a tooth that correspond to the growth of the animal (Figure 1). During summer and spring, growth is fast which accounts for the white area, but during winter, growth slows down and the cementum is compressed which accounts for a darkened line. In females, the relationship between cementum width declines and reproduction likely reflects the large expenditure of energy that is required during gestation and lactation. However, male and female mammals expend energy for reproduction in very distinct ways,3 and the same pattern of cementum decline may not be present in males. Since shifts in the life history strategy of males are poorly understood, we are interested in testing the relationship between cementum declines and reproduction in male sea otters using cementum analysis.

Ethnicity and Disease↗