Geology topics

Marc R. Matchett

Publications and source records attributed to Marc R. Matchett.

At least 19 recordsLinked to original sources

USGS2026

Fipronil baits as emerging tools for flea control and plague mitigation: Experiments with cricetid mice on prairie dog colonies

Plague is a zoonotic disease of mammalian hosts and flea vectors. Wildlife biologists most commonly mitigate plague by controlling flea populations. We evaluated the efficacy of edible baits for systemic flea control with two cricetid species on colonies of black-tailed prairie dogs ( Cynomys ludovicianus ): the western deer mouse ( Peromyscus sonoriensis ) and the northern grasshopper mouse ( Onychomys leucogaster ). We tested grain bait with 0.005% fipronil by weight and “FipBit” pellets with 0.46–1.52 mg of fipronil/pellet. Flea prevalence was assessed via combing of live-trapped mice. In one experiment with fipronil grain bait and FipBits ( n =564 combings), flea prevalence declined from 74% (grain) and 45% (FipBits) before treatments to 0% for both treatments from 30–44 d and from 324–413 d after treatments. During a second experiment with FipBits ( n =299 combings), flea prevalence declined from 13% to 32% before treatments to 0% from 11–15 d after treatments, but increased to 29–56% from 349–378 d after treatments. Results herein suggest annual fipronil bait treatments may be most effective for flea control.

Journal of Wildlife Diseases↗

USGS2026

Leucism in a family group and a review of color aberrations in Burrowing Owls ( Athene cunicularia )

Avian color aberrations capture public interest and sometimes indicate ecological problems. Diagnosing color aberration type can be difficult because nomenclature is inconsistent, appearance of color aberrations vary, typical coloration varies, and there are many undocumented color aberration types. One type of recognized avian color aberration is leucism. Leucism is often colloquially used to refer to all birds that are paler than normal but not albino, but it specifically refers to a plumage aberration in which, from hatching onward, birds are either all white or have patches of bilaterally symmetrical white feathers mixed with normally colored feathers, while retaining black pupils. Here, we document a case of leucism in a family of North American Burrowing Owls ( Athene cunicularia ). We observed a family group (two adults and five juveniles) of five leucistic, nearly all white owls, and two typically colored owls, in the Conata Basin, South Dakota, USA, in summer 2024. We also compiled all searchable records of color aberrations in Burrowing Owls across their North and South American range. We found 60 records of color aberrations, seven of which were cases of potential leucism. Twenty-five color aberrations were an unknown type in which only eye color was affected, all of them in Florida (USA) or south/central Brazil. Documenting color aberrations in birds can help expand our understanding of the types, causes, and consequences of color aberrations as well as the pigments and genetics that underly normal coloration.

South Dakota↗

USGS2026

Edible baits for systemic flea control, plague mitigation, and wildlife conservation: Evaluation of four active ingredients with three rodent species in western North America

The flea-borne agent of plague, Yersinia pestis , is lethal to endangered black-footed ferrets ( Mustela nigripes , BFFs) and the prairie dogs ( Cynomys spp., PDs) on which BFFs depend for habitat and prey. We developed bait pellets containing insecticides for flea control with PDs. Individual baits contained 0.46, 0.91, 1.21, or 1.52 mg fipronil, 5.40 mg afoxolaner, 50.62 mg fluralaner, or 85.20 mg spinosad. From 2023 to 2025, we tested the baits with black-tailed PDs ( C. ludovicianus , BTPDs), Gunnison's PDs ( C. gunnisoni , GPDs), and Richardson's ground squirrels ( Urocitellus richardsonii , RGSs). We sampled hosts 2810 times and detected 8825 fleas across 2 U.S. States, 1 Canadian Province, 6 sites, 9 PD colonies, and 41 sampling plots. Over ∼12 mo across 5 replicates in South Dakota, USA, bait pellets with 0.91 or 1.52 mg fipronil, applied at a rate of 125 baits/ha, were more effective in reducing the abundance of fleas on BTPDs than 0.46 mg fipronil or the 3 other active ingredients; on 2 South Dakota replicates with data from 24 mo posttreatment, the effects of fipronil pellets on flea abundance had waned after ∼24 mo. Similarly, over ∼12 mo on 2 replicates in Arizona, USA, pellets with 1.52 mg fipronil were more effective in reducing the abundance of fleas on GPDs than pellets with 0.46 mg fipronil; on 1 replicate with available data from ∼2 yr posttreatment, the effects of fipronil pellets had waned after ∼24 mo. Over ∼8-11 mo across 2 replicates in Saskatchewan, Canada, baits with 1.21 mg fipronil/pellet were more effective in suppressing the abundance of fleas on BTPDs and RGSs when applied at 250 pellets/ha than 62 pellets/ha; flea control had waned after ∼20-23 mo. When applied annually at 125-250/ha, baits with 0.84-1.52 mg fipronil (FipBits) provided an effective, efficient, and affordable tool for flea control on PD colonies.

Arizona, Saskatchewan, South Dakota↗

USGS2026

Effects of fipronil bait pellets on two cricetid species: Potential implications for plague mitigation and wildlife conservation

We evaluated the effects of fipronil bait pellets on two cricetids that commonly occupy colonies of black-tailed prairie dogs ( Cynomys ludovicianus ; BTPDs): western deer mice ( Peromyscus sonoriensis ) and northern grasshopper mice ( Onychomys leucogaster ). In one experiment, bait pellets (0.96 mg fipronil/bait) were applied at 75 baits/ha to three 1.44-ha plots on a BTPD colony. Mouse abundance declined by 70% from before to 6-10 d after treatment. In a second experiment, bait pellets (0.46 or 1.52 mg fipronil/bait) were applied at 125 baits/ha to four plots (0.85-1.86 ha) on two BTPD colonies; two non-treated plots were baselines (1.09 and 2.06 ha). From before to 11-15 d after treatment, mouse abundance declined by 51%- 67% on the treated plots vs. a decline of 9% on the non-treated plots. Mouse survival from before to 11-15 d after treatment was 51% lower on the treated plots. In a third experiment, bait pellets (0.84 mg fipronil/bait) were applied at 125 baits/acre on two 1.44-ha plots on a BTPD colony; two 1.44-ha non-treated plots were baselines. Mouse survival from before to 30-44 d after treatment was 45% lower on the treated plots; the abundance of deer mice on the treated plots remained similar from before to 30-44 d after treatment, perhaps due to juvenile recruitment and/or immigration. In a laboratory experiment, 33 deer mice offered one bait pellet (0.86 mg fipronil/bait) consumed 27% of their bait, on average (range = 0-100%). Over 3 d, deer mouse mortality was estimated at 53%; mortality increased with fipronil dose, which averaged 11 mg fipronil/kg body mass (range = 3-46 mg/kg). Brain samples were available from 31 deer mice; all tested positive for fipronil sulfone, the primary mammalian metabolite of fipronil, at 19 to 61,205 ng fipronil sulfone/g. Additional experiments could determine if these findings scale up to larger landscapes.

South Dakota↗

USGS2023

Alternative lifestyles: A plague persistence hypothesis

Several explanations have been posited for how the plague bacterium ( Yersinia pestis ) reemerges during sylvatic cycles within the same foci over many years, and often without direct evidence of host die-offs. One prevalent view is that transmission-optimized Y. pestis bacteria, exhibiting epizootic/enzootic behavior, almost continually replicate and survive through repeated, linked, host-centered propagation events. These bacteria, we will refer to as “ r-pestis ” type ecotype(s), represent a limited number of phenotypic lineages exhibiting optimal transmissibility and high rates of reproduction. These attributes, it is thought, assure their durability through time. For continuous r-pestis type expansions to be successful, adequate numbers of fleas and hosts must become infected to produce massive numbers of bacteria. In the process, host and flea numbers decline as they succumb to plague. Here we hypothesize that r-pestis population expansions seed the environment and confront a unique, highly competitive local milieu, where natural selection favors new ecotypes that incorporate a range of emergent adaptive survival strategies. These newly adapted survivors we recognize as a range of “ K - pestis ” ecotypes with greater durability and lower reproduction rates. These emergent K - pestis forms may arise in succession or coexist for varying periods of time with r-pestis ecotypes, and with other K - pestis ecotypes. Among K-pestis ecotypes, we hypothesize that through adaptive radiations, some persist within flea life stages, soil, organic waste, amoebae, plants, carcasses, hosts, or within niches yet to be characterized. In some settings, after a long quiet period, when favorable, K-pestis bacteria may trigger a singular event where an r-pestis transmission stream emerges precipitating another enzootic/epizootic progression. If this hypothesis withstands rigorous testing, then Y. pestis might represent an even more formidable, enduring, and adaptable foe, where unforeseen local events could trigger new epidemic and epizootic/enzootic events threatening humans and populations of other mammals, including those of conservation concern.

Ecosphere↗

USGS2023

Flea control on prairie dogs (Cynomys spp.) with fipronil bait pellets: Potential plague mitigation tool for rapid field application and wildlife conservation

Sylvatic plague is a widespread, primarily flea-vectored disease in western North America. Because plague is highly lethal to endangered black-footed ferrets ( Mustela nigripes , BFFs) and the prairie dogs ( Cynomys spp., PDs) on which BFFs depend for habitat and prey, minimizing the impacts of plague is a priority at BFF reintroduction sites. We developed a new, flour-based bait pellet containing 0.84 mg of fipronil and weighing ∼1.25 g (FipBits). We measured the degree and duration of flea control on black-tailed PDs ( C. ludovicianus ) in Montana and on Gunnison's PDs ( C. gunnisoni ) in Arizona, USA from 2018–2020. FipBits were distributed on treated plots one time at a rate of 125/ha. Fleas were virtually eliminated in Montana from 1 mo posttreatment to 1 yr later and remained substantially depressed 2 yr posttreatment. With the split colony design, we probably underestimated the degree of flea control achieved with FipBits due to crossover edge effects along the arbitrary line dividing the plots. Flea control in Arizona was significant from 1 mo posttreatment to 1 yr later, but flea abundance had recovered by 2 yr posttreatment. Flea control was evaluated from 2020–2021 in South Dakota, USA on four plots treated with three concentrations of fipronil in FipBits (0.68, 0.71, and 0.83 mg/FipBit). Fleas were essentially eliminated for 10 mo on the 0.83-mg plot and were substantially reduced on the two 0.71-mg plots. Fleas were reduced on the 0.68-mg plot, but the degree of control was less than observed on other treated plots. Impacts of plague on PDs and BFFs would probably be greatly reduced by the levels of flea control observed with FipBits. Options for expanded FipBit evaluations are being pursued for what may become a highly practical, affordable, and effective plague mitigation tool.

Arizona, Montana, South Dakota↗

USGS2023

Evaluating baits with lufenuron and nitenpyram for flea control on prairie dogs (Cynomys spp.) to mitigate plague

Plague, caused by Yersinia pestis , is a widespread threat to endangered black-footed ferrets ( Mustela nigripes ) and their primary prey, prairie dogs ( Cynomys spp.). Wildlife biologists most commonly manage plague using insecticides to control fleas, the primary vectors of Y. pestis . We tested edible baits containing the insecticides lufenuron and/or nitenpyram in prairie dogs. During a laboratory study, we treated 26 white-tailed prairie dogs ( Cynomys leucurus ) with lufenuron at 300 mg/kg body mass. All animals remained clinically healthy over the 9 wk monitoring period. Although serum lufenuron concentrations were >130 ppb in two treatment groups at week 1, concentrations declined to ≤60 ppb after 3 wk in non-torpid prairie dogs and after 7 wk in torpid prairie dogs. In a field experiment, we tested baits containing a combination of 75 mg lufenuron and 6 mg nitenpyram, respectively, in black-tailed prairie dogs ( Cynomys ludovicianus ). We uniformly distributed baits at 125 baits/ha on two plots (treated once) and 250 baits/ha on two plots (each treated twice 4.4 wk apart). Following treatments, flea abundance increased on prairie dogs and remained stable in burrows. Our findings indicate that baits containing lufenuron and nitenpyram, at the reported treatment rates, are ineffective tools for flea control on prairie dogs. Future experiments might evaluate efficacy of higher doses of lufenuron and nitenpyram, and repetitive treatments at differing intervals over time to evaluate potentially therapeutic treatments.

Journal of Wildlife Diseases↗

USGS2022

Exploring and mitigating plague for One Health purposes

Purpose of Review In 2020, the Appropriations Committee for the U.S. House of Representatives directed the CDC to develop a national One Health framework to combat zoonotic diseases, including sylvatic plague, which is caused by the flea-borne bacterium Yersinia pestis . This review builds upon that multisectoral objective. We aim to increase awareness of Y. pestis and to highlight examples of plague mitigation for One Health purposes (i.e., to achieve optimal health outcomes for people, animals, plants, and their shared environment). We draw primarily upon examples from the USA, but also discuss research from Madagascar and Uganda where relevant, as Y. pestis has emerged as a zoonotic threat in those foci. Recent Findings Historically, the bulk of plague research has been directed at the disease in humans. This is not surprising, given that Y. pestis is a scourge of human history. Nevertheless, the ecology of Y. pestis is inextricably linked to other mammals and fleas under natural conditions. Accumulating evidence demonstrates Y. pestis is an unrelenting threat to multiple ecosystems, where the bacterium is capable of significantly reducing native species abundance and diversity while altering competitive and trophic relationships, food web connections, and nutrient cycles. In doing so, Y. pestis transforms ecosystems, causing “shifting baselines syndrome” in humans, where there is a gradual shift in the accepted norms for the condition of the natural environment. Eradication of Y. pestis in nature is difficult to impossible, but effective mitigation is achievable; we discuss flea vector control and One Health implications in this context. Summary There is an acute need to rapidly expand research on Y. pestis , across multiple host and flea species and varied ecosystems of the Western US and abroad, for human and environmental health purposes. The fate of many wildlife species hangs in the balance, and the implications for humans are profound in some regions. Collaborative multisectoral research is needed to define the scope of the problem in each epidemiological context and to identify, refine, and implement appropriate and effective mitigation practices.

Current Tropical Medicine Reports↗

USGS2022

Reevaluation of the role of blocked Oropsylla hirsuta prairie dog fleas (Siphonaptera: Ceratophyllidae) in Yersinia pestis (Enterobacterales: Enterobacteriaceae) transmission

Prairie dogs in the western United States experience periodic epizootics of plague, caused by the flea-borne bacterial pathogen Yersinia pestis . An early study indicated that Oropsylla hirsuta (Baker), often the most abundant prairie dog flea vector of plague, seldom transmits Y. pestis by the classic blocked flea mechanism. More recently, an alternative early-phase mode of transmission has been proposed as the driving force behind prairie dog epizootics. In this study, using the same flea infection protocol used previously to evaluate early-phase transmission, we assessed the vector competence of O. hirsuta for both modes of transmission. Proventricular blockage was evident during the first two weeks after infection and transmission during this time was at least as efficient as early-phase transmission 2 d after infection. Thus, both modes of transmission likely contribute to plague epizootics in prairie dogs.

Journal of Medical Entomology↗

USGS2021

Comparison of flea sampling methods and Yersinia pestis detection on prairie dog colonies

Scientists collect fleas (Siphonaptera) to survey for Yersinia pestis , the bacterial agent of plague. When studying fleas parasitizing prairie dogs ( Cynomys spp.), two primary methods are used: (1) combing fleas from live-trapped prairie dogs and (2) swabbing fleas from burrows with cloth swabs attached to metal cables. Ideally, burrow swabbing, the cheaper and easier method, would explain flea burdens on prairie dogs and provide reliable information on plague prevalence. In a linear regression analysis of data from 1-month intervals (June–August 2010–2011) on 13 colonies of black-tailed prairie dogs ( Cynomys ludovicianus , BTPDs) in New Mexico, flea abundance on swabs explained 0–26% of variation in BTPD flea burdens. In an analysis of data (May–August 2016) from six colonies of BTPDs in Montana, flea abundance on swabs explained 2% of variation in BTPD flea burdens. In an analysis of data from a short-term interval (July 23–27, 2019) on four colonies of BTPDs in Montana, flea abundance on swabs explained 0.1% of variation in BTPD flea burdens. In an analysis of data from 1-week intervals (August–October 2000) on four colonies of white-tailed prairie dogs ( Cynomys leucurus , WTPD) in Utah, swabbing data explained 0.1% of variation in WTPD flea burdens. Pools of fleas from two WTPD colonies were tested for Y. pestis by mouse inoculation and isolation; 65% from WTPDs tested positive, whereas 4% from burrows tested positive. Data herein also show that results from burrow swabbing can misrepresent flea species composition and phenology on prairie dogs. Burrow swabbing is useful for some purposes, but limitations should be acknowledged, and accumulated data should be interpreted with caution.

Montana, New Mexico, Utah↗

USGS2021

Oral sylvatic plague vaccine does not adequately protect prairie dogs (Cynomys spp.) for endangered black-footed ferret (Mustela nigripes) conservation

The plague bacterium Yersinia pestis is lethal to endangered black-footed ferrets ( Mustela nigripes , BFF) and the prairie dogs ( Cynomys spp., PD) on which they depend for habitat and prey. We assessed the effectiveness of an oral sylvatic plague vaccine delivered in baits to black-tailed PD ( Cynomys ludovicianus , BTPD) from 2013 to 2017 on the Charles M. Russell National Wildlife Refuge (CMR) in northcentral Montana. We permanently marked BTPD on four paired vaccine ( N = 1,349 individuals) and placebo plots ( N = 926; 7,027 total captures). We analyzed capture–recapture data under a Cormack–Jolly–Seber model to estimate annual apparent survival. Overall, survival averaged 0.05 lower on vaccine plots than on paired placebo plots. Immediately before noticeable die-offs and detecting plague on pairs CMR1 and CMR2, 89% of BTPD sampled on vaccine plots had consumed at least one bait and the immune systems (pleural) of 40% were likely boosted by consuming baits over multiple years. Survival to the following year was 0.16 and 0.05 on the vaccine plots and 0.19 and 0.06 on the placebo plots for pairs CMR1 and CMR2, respectively. These rates were markedly lower than 0.63, the overall average estimate on those same plots during the previous 3 years. PD populations subjected to such large die-offs would not be expected to sustain a BFF population. An overriding limitation to achieving sufficient protection rests with vaccine delivery constraints. Late summer/fall bait distribution results in the highest bait uptake rates. However, the PD birth pulse each spring can double the size of populations in most years, greatly reducing the proportion of vaccinates in populations and diminishing potential herd immunity benefits. In addition to nonvaccinated juveniles and PD that do not consume bait, incomplete vaccine protection and time required for immunity to develop leaves a large majority of PD populations vulnerable to plague for 6–7 months or more each year.

Montana↗

USGS2017

Factors influencing uptake of sylvatic plague vaccine baits by prairie dogs

Sylvatic plague vaccine (SPV) is a virally vectored bait-delivered vaccine expressing Yersinia pestis antigens that can protect prairie dogs (Cynomys spp.) from plague and has potential utility as a management tool. In a large-scale 3-year field trial, SPV-laden baits containing the biomarker rhodamine B (used to determine bait consumption) were distributed annually at a rate of approximately 100–125 baits/hectare along transects at 58 plots encompassing the geographic ranges of four species of prairie dogs. We assessed site- and individual-level factors related to bait uptake in prairie dogs to determine which were associated with bait uptake rates. Overall bait uptake for 7820 prairie dogs sampled was 70% (95% C.I. 69.9–72.0). Factors influencing bait uptake rates by prairie dogs varied by species, however, in general, heavier animals had greater bait uptake rates. Vegetation quality and day of baiting influenced this relationship for black-tailed, Gunnison’s, and Utah prairie dogs. For these species, baiting later in the season, when normalized difference vegetation indices (a measure of green vegetation density) are lower, improves bait uptake by smaller animals. Consideration of these factors can aid in the development of species-specific SPV baiting strategies that maximize bait uptake and subsequent immunization of prairie dogs against plague.

EcoHealth↗

USGS2017

Sylvatic plague vaccine partially protects prairie dogs (Cynomys spp.) in field trials

Sylvatic plague, caused by Yersinia pestis , frequently afflicts prairie dogs ( Cynomys spp.), causing population declines and local extirpations. We tested the effectiveness of bait-delivered sylvatic plague vaccine (SPV) in prairie dog colonies on 29 paired placebo and treatment plots (1–59 ha in size; average 16.9 ha) in 7 western states from 2013 to 2015. We compared relative abundance (using catch per unit effort (CPUE) as an index) and apparent survival of prairie dogs on 26 of the 29 paired plots, 12 with confirmed or suspected plague ( Y. pestis positive carcasses or fleas). Even though plague mortality occurred in prairie dogs on vaccine plots, SPV treatment had an overall positive effect on CPUE in all three years, regardless of plague status. Odds of capturing a unique animal were 1.10 (95% confidence interval [C.I.] 1.02–1.19) times higher per trap day on vaccine-treated plots than placebo plots in 2013, 1.47 (95% C.I. 1.41–1.52) times higher in 2014 and 1.19 (95% C.I. 1.13–1.25) times higher in 2015. On pairs where plague occurred, odds of apparent survival were 1.76 (95% Bayesian credible interval [B.C.I.] 1.28–2.43) times higher on vaccine plots than placebo plots for adults and 2.41 (95% B.C.I. 1.72–3.38) times higher for juveniles. Our results provide evidence that consumption of vaccine-laden baits can protect prairie dogs against plague; however, further evaluation and refinement are needed to optimize SPV use as a management tool.

EcoHealth↗

USGS2015

Linking resource selection and mortality modeling for population estimation of mountain lions in Montana

To be most effective, the scale of wildlife management practices should match the range of a particular species’ movements. For this reason, combined with our inability to rigorously or regularly census mountain lion populations, several authors have suggested that mountain lions be managed in a source-sink or metapopulation framework. We used a combination of resource selection functions, mortality estimation, and dispersal modeling to estimate cougar population levels in Montana statewide and potential population level effects of planned harvest levels. Between 1980 and 2012, 236 independent mountain lions were collared and monitored for research in Montana. From these data we used 18,695 GPS locations collected during winter from 85 animals to develop a resource selection function (RSF), and 11,726 VHF and GPS locations from 142 animals along with the locations of 6343 mountain lions harvested from 1988–2011 to validate the RSF model. Our RSF model validated well in all portions of the State, although it appeared to perform better in Montana Fish, Wildlife and Parks (MFWP) Regions 1, 2, 4 and 6, than in Regions 3, 5, and 7. Our mean RSF based population estimate for the total population (kittens, juveniles, and adults) of mountain lions in Montana in 2005 was 3926, with almost 25% of the entire population in MFWP Region 1. Estimates based on a high and low reference population estimates produce a possible range of 2784 to 5156 mountain lions statewide. Based on a range of possible survival rates we estimated the mountain lion population in Montana to be stable to slightly increasing between 2005 and 2010 with lambda ranging from 0.999 (SD = 0.05) to 1.02 (SD = 0.03). We believe these population growth rates to be a conservative estimate of true population growth. Our model suggests that proposed changes to female harvest quotas for 2013–2015 will result in an annual statewide population decline of 3% and shows that, due to reduced dispersal, changes to harvest in one management unit may affect population growth in neighboring units where smaller or even no changes were made. Uncertainty regarding dispersal levels and initial population density may have a significant effect on predictions at a management unit scale (i.e. 2000 km 2 ), while at a regional scale (i.e. 50,000 km 2 ) large differences in initial population density result in relatively small changes in population growth rate, and uncertainty about dispersal may not be as influential. Doubling the presumed initial density from a low estimation of 2.19 total animals per 100 km 2 resulted in a difference in annual population growth rate of only 2.6% statewide when compared to high density of 4.04 total animals per 100 km 2 (low initial population estimate λ = 0.99, while high initial population estimate λ = 1.03). We suggest modeling tools such as this may be useful in harvest planning at a regional and statewide level.

Ecological Modelling↗

USGS2012

Resource selection models are useful in predicting fine-scale distributions of black-footed ferrets in prairie dog colonies

Wildlife-habitat relationships are often conceptualized as resource selection functions (RSFs)—models increasingly used to estimate species distributions and prioritize habitat conservation. We evaluated the predictive capabilities of 2 black-footed ferret ( Mustela nigripes ) RSFs developed on a 452-ha colony of black-tailed prairie dogs ( Cynomys ludovicianus ) in the Conata Basin, South Dakota. We used the RSFs to project the relative probability of occurrence of ferrets throughout an adjacent 227-ha colony. We evaluated performance of the RSFs using ferret space use data collected via postbreeding spotlight surveys June–October 2005–2006. In home ranges and core areas, ferrets selected the predicted "very high" and "high" occurrence categories of both RSFs. Count metrics also suggested selection of these categories; for each model in each year, approximately 81% of ferret locations occurred in areas of very high or high predicted occurrence. These results suggest usefulness of the RSFs in estimating the distribution of ferrets throughout a black-tailed prairie dog colony. The RSFs provide a fine-scale habitat assessment for ferrets that can be used to prioritize releases of ferrets and habitat restoration for prairie dogs and ferrets. A method to quickly inventory the distribution of prairie dog burrow openings would greatly facilitate application of the RSFs.

South Dakota↗

USGS2011

Resource selection by black-footed ferrets in South Dakota and Montana

The black-footed ferret (Mustela nigripes), once extinct in the wild, remains one of the most critically endangered mammals in North America despite 18 years of reintroduction attempts. Because black-footed ferrets are specialized predators of prairie dogs (Cynomys sp.), a better understanding of how black-footed ferrets select resources might provide insight into how best to identify and manage reintroduction sites. We monitored ferret resource selection at two reintroduction sites with different densities of prairie dog populations-one that contained a high density of prairie dogs (Conata Basin, South Dakota) and one that was lower (UL Bend, Montana). We evaluated support for hypotheses about ferret resource selection as related to the distribution of active burrows used by black-tailed prairie dogs (Cynomys ludovicianus), interactions between ferrets, and habitat edge effects. We found support for all three factors within both populations; however, they affected ferret resource selection differently at each site. Ferrets at Conata Basin tended to select areas with high prairie dog burrow density, closer to the colony edge, and that overlapped other ferret ranges. In contrast, ferrets at UL Bend tended not to select areas of high active prairie dog burrow density, avoided areas close to edge habitat, and females avoided areas occupied by other ferrets. The differences observed between the two sites might be best explained by prairie dog densities, which were higher at Conata Basin (119.3 active burrows per ha) than at UL Bend (44.4 active burrows per ha). Given the positive growth of ferret populations at Conata Basin, management that increases the density of prairie dogs might enhance ferret success within natural areas. To achieve long-term recovery of ferrets in the wild, conservationists should increasingly work across and outside natural area boundaries to increase prairie dog populations.

Natural Areas Journal↗

USGS2010

Enzootic plague reduces black-footed ferret (Mustela nigripes) survival in Montana

Black-footed ferrets ( Mustela nigripes ) require extensive prairie dog colonies ( Cynomys spp.) to provide habitat and prey. Epizootic plague kills both prairie dogs and ferrets and is a major factor limiting recovery of the highly endangered ferret. In addition to epizootics, we hypothesized that enzootic plague, that is, presence of disease-causing Yersinia pestis without any noticeable prairie dog die off, may also affect ferret survival. We reduced risk of plague on portions of two ferret reintroduction areas by conducting flea control for 3 years. Beginning in 2004, about half of the ferrets residing on dusted and nondusted colonies were vaccinated against plague with an experimental vaccine (F1-V fusion protein). We evaluated 6-month reencounter rates (percentage of animals observed at the end of an interval that were known alive at the beginning of the interval), an index to survival, for ferrets in four treatment groups involving all combinations of vaccination and flea control. For captive-reared ferrets (115 individuals observed across 156 time intervals), reencounter rates were higher for vaccinates (0.44) than for nonvaccinates (0.23, p  = 0.044) on colonies without flea control, but vaccination had no detectable effect on colonies with flea control (vaccinates = 0.41, nonvaccinates = 0.42, p  = 0.754). Flea control resulted in higher reencounter rates for nonvaccinates ( p  = 0.026), but not for vaccinates ( p  = 0.508). The enhancement of survival due to vaccination or flea control supports the hypothesis that enzootic plague reduces ferret survival, even when there was no noticeable decline in prairie dog abundance. The collective effects of vaccination and flea control compel a conclusion that fleas are required for maintenance, and probably transmission, of plague at enzootic levels. Other studies have demonstrated similar effects of flea control on several species of prairie dogs and, when combined with this study, suggest that the effects of enzootic plague are widespread. Finally, we demonstrated that the experimental F1-V fusion protein vaccine provides protection to ferrets in the wild.

Vector-Borne and Zoonotic Diseases↗

USGS2008

Implications of black-tailed prairie dog spatial dynamics to black-footed ferrets

The spatial dynamics of black-tailed prairie dog (Cynomys ludovicianus) colonies affect the utility of these environments for other wildlife, including the endangered black-footed ferret (Mustela nigripes). We used location data of active and inactive black-tailed prairie dog burrows to investigate colony structure, spatial distribution, and patch dynamics of two colonies at ferret recovery sites. We used kernel-based utilization distributions (UDs) of active and inactive burrows from two time periods (six and 11 years apart) as the basis for our analysis. Overall, the total extent of our prairie dog colonies changed little over time. However, within colonies, areas with high densities of active and inactive prairie dog burrows formed patches and the distribution of these patches changed in size, shape, and connectivity over time. At the Conata Basin site, high-density active burrow patches increased in total area covered while decreasing in connectivity as they shifted towards the perimeter of the colony over time. At the UL Bend site, we observed a similar but less pronounced shift over a longer period of time. At both sites, while at a large scale it appeared that prairie dogs were simply shifting areas of activity towards the perimeter of colonies and abandoning the center of colonies, we observed a dynamic interaction between areas of active and inactive burrows within colonies over time. Areas that previously contained inactive burrows tended to become active, and vice versa, leading us to hypothesize that there are shifts of activity areas within colonies over time as dictated by forage availability. The spatial dynamics we observed have important implications for techniques to estimate the suitability of ferret habitat and for the management of prairie dog colonies. First, fine-scale techniques for measuring prairie dog colonies that account for their patchy spatial distribution are needed to better assess ferret habitat suitability. Second, the shift of high-density areas of active prairie dog burrows, likely associated with changes in vegetation, suggests that through the management of vegetation we might be able to indirectly improve habitat for ferrets. Finally, we found that prairie dog distributions within a colony are a naturally dynamic process and that management strategies should consider the long-term value of both active and inactive areas within colonies.

Natural Areas Journal↗