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Gary W. Roemer

Publications and source records attributed to Gary W. Roemer.

13 recordsLinked to original sources

Abundance estimates of Gunnison’s prairie dogs compared to the number of active burrows

Reliable estimates of prairie dog ( Cynomys spp.) population size and distribution are critical for assessing the status of prairie dogs and for selecting sites to reintroduce black-footed ferrets ( Mustela nigripes ). The density of active prairie dog burrows has commonly been used as an index of prairie dog abundance. Indices derived from active burrow counts were developed for black-tailed ( C. ludovicianus ) and white-tailed ( C. leucurus ) prairie dogs, but their efficacy has not been evaluated for all prairie dog species and studies affirming their validity with robust abundance estimators are few. We indexed or estimated the abundance of Gunnison's prairie dogs ( C. gunnisoni ) in the Aubrey Valley, Arizona, USA, in 2006 at 2 different time periods using 4 different methods—maximum above ground counts (MAGC), minimum number known alive (MNKA), capture-mark-recapture (CMR), and mark-resight—and compared these estimates to active burrow counts in 2005 and 2006. We found no positive relationship between active burrow counts and any abundance estimators. Mark-resight estimates of abundance were greater than the MNKA and were positively correlated with both the MNKA ( r 2 = 0.30) and CMR estimates ( r 2 = 0.49). Both CMR estimates and MAGC were typically below the MNKA and therefore biased low. Our results indicated that more rigorous estimation methods may be necessary to accurately estimate prairie dog abundance and assess habitat quality for ferret conservation.

Arizona

Habitat selection and water dependency of feral burros in the Mojave Desert, California, USA

Expansion of feral burro ( Equus asinus ) populations across the southwestern United States is causing human–wildlife conflicts including rangeland degradation, competition with livestock and native species, and burro–vehicle collisions. On the Fort Irwin National Training Center (NTC) in California, feral burros interfere with military training and are involved in vehicle collisions and other conflicts (e.g., burros blocking access to buildings). Limited data on burro movements and resource use poses a challenge for the development of management plans and mitigation strategies. We estimated home range size, second- and third-order seasonal resource selection, and water dependency of 10 adult female feral burros fitted with global positioning system (GPS) collars on the NTC from November 2015 to April 2017. Mean 95% autocorrelated kernel home range size of female burros (253.9 ± 30.7 km 2 [SE]) did not differ among seasons or between burros that resided close to or far from urban areas. Burros selected areas closer to water in all seasons and at both spatial scales, but selection was stronger in the dry season and at the landscape scale. When available, burros strongly selected for areas closer to urban areas. Burros consistently selected for areas with green forage and at lower elevations, but selection for other topographical features was variable. Water use patterns were consistent with the resource selection results. Burros visited water sources twice as often (every 22.2 ± 6.3 hr) during the hot-dry season (Apr–Oct) compared to the cool-wet seasons (Nov–Mar; 2015: 45.9 ± 21.0; 2016: 39.7 ± 9.3 hr). Our results suggest that urban areas, and resources therein, and water sources have the biggest influence on burro resource selection, and management plans could focus mitigation programs on these areas.

California

A 37 K SNP array for the management and conservation of Golden Eagles (Aquila chrysaetos)

We describe the development of a custom 37 K Affymetrix Axiom myDesign single nucleotide polymorphism (SNP) array for a culturally and ecologically important apex predator, the golden eagle ( Aquila chrysaetos ). Using this SNP array, we performed population genomic analysis on 154 individuals of known natal localities and detected three genetic clusters that we designated as Taiga/High Arctic, Great Basin, and Rocky Mountains/Great Plains. Each of these clusters appears to display clinal variation within these geographic regions. After determining genetic structure, we performed an assignment test of 32 individuals, five of which were siblings of individuals used in the assessment of genetic structure, three had associated telemetry data, and the remaining individuals were of unknown natal locations. Using this array, four siblings were correctly assigned to the same geographic region as their sibling and the genetic assignment of the radio telemetered birds agreed with the expected movement patterns displayed by these individuals. For the remaining individuals, we were able to assign all but five individuals to one of the three genetic clusters. Our genetic assignments illustrates the utility of this SNP array to accurately assign most individuals to predesignated geographical regions. While further compiling genetic and other data types, we can increase the power of this tool for identifying those breeding populations that may need assistance due to anthropogenic stressors that negatively impact their population viability. The use of this genetic resource will help substantiate decisions by multiple conservation groups that seek to preserve the natural population structure of the golden eagle.

Conservation Genetics

Anthropogenic subsidies influence resource use during a mange epizootic in a desert coyote population

Colonization of urban areas by synanthropic wildlife introduces novel and complex alterations to established ecological processes, including the emergence and spread of infectious diseases. Aggregation at urban resources can increase disease transfer, with wide-ranging species potentially infecting outlying populations. The garrison at the National Training Center, Fort Irwin, California, USA, was recently colonized by mange-infected coyotes ( Canis latrans ) that also use the surrounding Mojave Desert. This situation provided an ideal opportunity to examine the effects of urban resources on disease dynamics. We evaluated seasonal space use and determined the influence of anthropogenic subsidies, water sources, and prey density on urban resource selection. We found no difference in home range size between healthy and infected individuals, but infected residents had considerably more spatial overlap with one another than healthy residents. All coyotes selected for anthropogenic subsidies during all seasons, while infected coyotes seasonally selected for urban water sources, and healthy coyotes seasonally selected for urban areas with greater densities of natural prey. These results suggest that while all coyotes were selecting for anthropogenic subsidies, infected resident coyotes demonstrated a greater tolerance for other conspecifics, which could be facilitating the horizontal transfer of sarcoptic mange to non-resident coyotes. Conversely, healthy coyotes also selected for natural prey and healthy residents exhibited a lack of spatial overlap with other coyotes suggesting they were not reliant on anthropogenic subsidies and were maintaining territories. Understanding the association between urban wildlife, zoonotic diseases, and urban resources can be critical in determining effective responses for mitigating future epizootics.

California

Pleistocene–Holocene vicariance, not Anthropocene landscape change, explains the genetic structure of American black bear (Ursus americanus) populations in the American Southwest and northern Mexico

The phylogeography of the American black bear ( Ursus americanus ) is characterized by isolation into glacial refugia, followed by population expansion and genetic admixture. Anthropogenic activities, including overharvest, habitat loss, and transportation infrastructure, have also influenced their landscape genetic structure. We describe the genetic structure of the American black bear in the American Southwest and northern Mexico and investigate how prehistoric and contemporary forces shaped genetic structure and influenced gene flow. Using a suite of microsatellites and a sample of 550 bears, we identified 14 subpopulations organized hierarchically following the distribution of ecoregions and mountain ranges containing black bear habitat. The pattern of subdivision we observed is more likely a product of postglacial habitat fragmentation during the Pleistocene and Holocene, rather than a consequence of contemporary anthropogenic barriers to movement during the Anthropocene. We used linear mixed-effects models to quantify the relationship between landscape resistance and genetic distance among individuals, which indicated that both isolation by resistance and geographic distance govern gene flow. Gene flow was highest among subpopulations occupying large tracts of contiguous habitat, was reduced among subpopulations in the Madrean Sky Island Archipelago, where montane habitat exists within a lowland matrix of arid lands, and was essentially nonexistent between two isolated subpopulations. We found significant asymmetric gene flow supporting the hypothesis that bears expanded northward from a Pleistocene refugium located in the American Southwest and northern Mexico and that major highways were not yet affecting gene flow. The potential vulnerability of the species to climate change, transportation infrastructure, and the US–Mexico border wall highlights conservation challenges and opportunities for binational collaboration.

Arizona, New Mexico, Utah, Wyoming

Accounting for residual heterogeneity in double-observer sightability models decreases bias in burro abundance estimates

Feral burros ( Equus asinus ) and horses ( E. ferus caballus ) inhabiting public land in the western United States are intended to be managed at population levels established to promote a thriving, natural ecological balance. Double-observer sightability (M DS ) models, which use detection records from multiple observers and sighting covariates, perform well for estimating feral horse abundances, but their effectiveness for use in burro populations is less understood. These M DS models help minimize detection bias, yet bias can be further reduced with models that account for unmodeled variation, or residual heterogeneity, in detection probability. In populations containing radio-marked individuals, residual heterogeneity can be estimated with M DS models by including a covariate that corresponds to the marked status of a group (M H models). Another approach is to use information from detections missed by both observers to account for the characteristics that make groups more or less likely to be detected, or recaptured, by the second observer (M R models). We used aerial survey data from 3 burro populations (Sinbad Herd Management Area, UT [2016–2018], Lake Pleasant Herd Management Area, AZ [2017], and Fort Irwin National Training Center, CA [2016–2017]) to develop M DS models applicable for feral burros in the southwestern United States. Our objectives were to quantify precision and bias of standard M DS surveys for feral burros and to examine which model type for incorporating residual heterogeneity (M H or M R ) would result in the least-biased estimates of burro populations relative to the minimum number known alive (MNKA) within the Sinbad Herd Management Area. Standard M DS model estimates achieved a mean coefficient of variation of 0.08, while underestimating MNKA by an average of 27.1%. Accounting for residual heterogeneity through recapture probability in M R models resulted in estimates closer to MNKA than M H models (9.5% vs. 16.5% less than MNKA). Our results indicate that M DS models can achieve precise enough estimates to monitor feral burro populations, but they routinely produce negatively biased estimates. We encourage the use of radio-collars to reduce bias in future burro surveys by accounting for residual heterogeneity through M R models.

Journal of Wildlife Management

Estimating abundance and simulating fertility control in feral burros

Overabundant populations of feral equids are negatively impacting rangelands in the western United States. To effectively manage these populations, robust estimates of abundance and demography are necessary, as well as cost-effective methods of reducing abundance. We used a double-observer-sightability aerial survey method to estimate the number of feral burros (Equus asinus) occupying the Fort Irwin National Training Center (NTC), California, USA. We examined the efficacy of using porcine zona pellucida (PZP) immunocontraception as a control agent and used matrix population models to simulate how changes in demographic rates would influence abundance. We estimated there were 690 (CI: 618–752) feral burros within the surveyed area, but these are part of a much larger population that is not geographically isolated from those in the survey area. Sighting probabilities ranged from 0.19–0.98 and were most strongly influenced by distance from observer and group size. We estimated age-specific demographic rates at the NTC and compiled mean rates across burro populations in arid environments from the literature. Mean fecundity varied from 0.17 to 0.58 foals per adult female with younger females having lower fecundity. Mean survival was 0.90 for foals, 0.98 for yearlings, and 0.96 for adults. PZP vaccine treatment strategies that suppressed fertility for up to 10 years, predicted that burro abundance would be reduced by 67–88% after 15 years (compared with no treatment), but none of these strategies resulted in population extirpation. Our fieldwork also highlights the difficulty of administering PZP vaccination to large, free-ranging animals. Burro growth rates shifted from increasing to decreasing at adult survival rates below 0.84 and the population was predicted to become extirpated when adult survival declined below 0.60. In the absence of other methods to reduce burro numbers, our findings indicate that current formulations of PZP immunocontraception, which require multiple doses, would be inadequate for controlling population growth rates at the NTC and perhaps elsewhere. Development of longer-term fertility reduction agents and/or more efficient vaccine delivery techniques would likely improve the efficacy of fertility control for overabundant ungulate populations. Lack of geographic closure (physical barriers to migration) further complicates management efforts to reduce burro numbers.

California

Urbanization’s influence on the distribution of mange in a carnivore revealed with multistate occupancy models

Increasing urbanization and use of urban areas by synanthropic wildlife has increased human and domestic animal exposure to zoonotic diseases and exacerbated epizootics within wildlife populations. Consequently, there is a need to improve wildlife disease surveillance programs to rapidly detect outbreaks and refine inferences regarding spatiotemporal disease dynamics. Multistate occupancy models can address potential shortcomings in surveillance programs by accounting for imperfect detection and the misclassification of disease states. We used these models to explore the relationship between urbanization, slope, and the spatial distribution of sarcoptic mange in coyotes ( Canis latrans ) inhabiting Fort Irwin, California, USA. We deployed remote cameras across 180 sites within the desert surrounding the populated garrison and classified sites by mange presence or absence depending on whether a symptomatic or asymptomatic coyote was photographed. Coyotes selected flatter sites closer to the urban area with a high probability of use (0.845, 95% credible interval (CRI): 0.728, 0.944); site use decreased as the distance to urban areas increased (standardized β ^ "> β ˆ β^ = − 1.354, 95% CRI − 2.423, − 0.619). The probability of correctly classifying mange presence at a site also decreased further from the urban area and was probably related to the severity of mange infection. Severely infected coyotes, which were more readily identified as symptomatic, resided closer to the urban area and were most likely dependent on urban resources for survival; urban resources probably contributed to sustaining the disease. Multistate occupancy models represent a flexible framework for estimating the occurrence and spatial extent of observable infectious diseases, which can improve wildlife disease surveillance programs.

California

Validating the performance of occupancy models for estimating habitat use and predicting the distribution of highly-mobile species: A case study using the American black bear

Occupancy models have become a valuable tool for estimating wildlife-habitat relationships and for predicting species distributions. Highly-mobile species often violate the assumption that sampling units are geographically closed shifting the probability of occupancy to be interpreted as the probability of use. We used occupancy models, in conjunction with noninvasive sampling, to estimate habitat use and predict the distribution of a highly-mobile carnivore, the American black bear ( Ursus americanus ) in New Mexico, USA. The top model indicated that black bears use areas with higher primary productivity and fewer roads. The predictive performance of such models is rarely validated with independent data, so we validated our model predictions with 2-independent datasets. We first assessed the correlation between predicted and observed habitat use for 28 telemetry-collared bears in the Jemez Mountains. Predicted habitat use was positively correlated with observed use for all 3 years (2012: ρ = 0.81; 2013: ρ = 0.87; 2014: ρ = 0.90). We then predicted the probability of use within a cell where a bear mortality was documented using 2043 mortality locations from sport harvest, depredation, and vehicle collisions. The probability of habitat use at a mortality location was also positively correlated with observed use by the species (2012: ρ = 0.74; 2013: ρ = 0.89; 2014: ρ = 0.93). Our validation procedure supports the notion that occupancy models can be an effective tool for estimating habitat use and predicting the distribution of highly-mobile species when the assumption of geographic closure has been violated. Our findings may be of interest to studies that are estimating habitat use for highly-mobile species that are secretive or rare, difficult to capture, or expensive to monitor with other more intensive methods.

New Mexico

Density of American black bears in New Mexico

Considering advances in noninvasive genetic sampling and spatially explicit capture–recapture (SECR) models, the New Mexico Department of Game and Fish sought to update their density estimates for American black bear ( Ursus americanus ) populations in New Mexico, USA, to aide in setting sustainable harvest limits. We estimated black bear density in the Sangre de Cristo, Sandia, and Sacramento Mountains, New Mexico, 2012–2014. We collected hair samples from black bears using hair traps and bear rubs and used a sex marker and a suite of microsatellite loci to individually genotype hair samples. We then estimated density in a SECR framework using sex, elevation, land cover type, and time to model heterogeneity in detection probability and the spatial scale over which detection probability declines. We sampled the populations using 554 hair traps and 117 bear rubs and collected 4,083 hair samples. We identified 725 (367 male, 358 female) individuals. Our density estimates varied from 16.5 bears/100 km 2 (95% CI = 11.6–23.5) in the southern Sacramento Mountains to 25.7 bears/100 km 2 (95% CI = 13.2–50.1) in the Sandia Mountains. Overall, detection probability at the activity center (g0) was low across all study areas and ranged from 0.00001 to 0.02. The low values of g0 were primarily a result of half of all hair samples for which genotypes were attempted failing to produce a complete genotype. We speculate that the low success we had genotyping hair samples was due to exceedingly high levels of ultraviolet (UV) radiation that degraded the DNA in the hair. Despite sampling difficulties, we were able to produce density estimates with levels of precision comparable to those estimated for black bears elsewhere in the United States.

New Mexico

Estimating black bear density in New Mexico using noninvasive genetic sampling coupled with spatially explicit capture-recapture methods

During the 2004–2005 to 2015–2016 hunting seasons, the New Mexico Department of Game and Fish (NMDGF) estimated black bear abundance (Ursus americanus) across the state by coupling density estimates with the distribution of primary habitat generated by Costello et al. (2001). These estimates have been used to set harvest limits. For example, a density of 17 bears/100 km2 for the Sangre de Cristo and Sacramento Mountains and 13.2 bears/100 km2 for the Sandia Mountains were used to set harvest levels. The advancement and widespread acceptance of non-invasive sampling and mark-recapture methods, prompted the NMDGF to collaborate with the New Mexico Cooperative Fish and Wildlife Research Unit and New Mexico State University to update their density estimates for black bear populations in select mountain ranges across the state. We established 5 study areas in 3 mountain ranges: the northern (NSC; sampled in 2012) and southern Sangre de Cristo Mountains (SSC; sampled in 2013), the Sandia Mountains (Sandias; sampled in 2014), and the northern (NSacs) and southern Sacramento Mountains (SSacs; both sampled in 2014). We collected hair samples from black bears using two concurrent non-invasive sampling methods, hair traps and bear rubs. We used a gender marker and a suite of microsatellite loci to determine the individual identification of hair samples that were suitable for genetic analysis. We used these data to generate mark-recapture encounter histories for each bear and estimated density in a spatially explicit capture-recapture framework (SECR). We constructed a suite of SECR candidate models using sex, elevation, land cover type, and time to model heterogeneity in detection probability and the spatial scale over which detection probability declines. We used Akaike’s Information Criterion corrected for small sample size (AICc) to rank and select the most supported model from which we estimated density. We set 554 hair traps, 117 bear rubs and collected 4,083 hair samples. We identified 725 (367 M, 358 F) individuals; the sex ratio for each study area was approximately equal. Our density estimates varied within and among mountain ranges with an estimated density of 21.86 bears/100 km2 (95% CI: 17.83 – 26.80) for the NSC, 19.74 bears/100 km2 (95% CI: 13.77 – 28.30) in the SSC, 25.75 bears/100 km2 (95% CI: 13.22 – 50.14) in the Sandias, 21.86 bears/100 km2 (95% CI: 17.83 – 26.80) in the NSacs, and 16.55 bears/100 km2 (95% CI: 11.64 – 23.53) in the SSacs. Overall detection probability for hair traps and bear rubs, combined, was low across all study areas and ranged from 0.00001 to 0.02. We speculate that detection probabilities were affected by failure of some hair samples to produce a complete genotype due to UV degradation of DNA, and our inability to set and check some sampling devices due to wildfires in the SSC. Ultraviolet radiation levels are particularly high in New Mexico compared to other states where NGS methods have been used because New Mexico receives substantial amounts of sunshine, is relatively high in elevation (1,200 m – 4,000 m), and is at a lower latitude. Despite these sampling difficulties, we were able to produce density estimates for New Mexico black bear populations with levels of precision comparable to estimated black bear densities made elsewhere in the U.S. Our ability to generate reliable black bear density estimates for 3 New Mexico mountain ranges is attributable to our use of a statistically robust study design and analytical method. There are multiple factors that need to be considered when developing future SECR-based density estimation projects. First, the spatial extent of the population of interest and the smallest average home range size must be determined; these will dictate size of the trapping array and spacing necessary between hair traps. The number of technicians needed and access to the study areas will also influence configuration of the trapping array. We believe shorter sampling occasions could be implemented to reduce degradation of DNA due to UV radiation; this might help increase amplification rates and thereby increase both the number of unique individuals identified and the number of recaptures, improving the precision of the density estimates. A pilot study may be useful to determine the length of time hair samples can remain in the field prior to collection. In addition, researchers may consider setting hair traps and bear rubs in more shaded areas (e.g., north facing slopes) to help reduce exposure to UV radiation. To reduce the sampling interval it will be necessary to either hire more field personnel or decrease the number of hair traps per sampling session. Both of these will enhance detection of long-range movement events by individual bears, increase initial capture and recapture rates, and improve precision of the parameter estimates. We recognize that all studies are constrained by limited resources, however, increasing field personnel would also allow a larger study area to be sampled or enable higher trap density. In conclusion, we estimated the density of black bears in 5 study areas within 3 mountains ranges of New Mexico. Our estimates will aid the NMDGF in setting sustainable harvest limits. Along with estimates of density, information on additional demographic rates (e.g., survival rates and reproduction) and the potential effects that climate change and future land use may have on the demography of black bears may also help inform management of black bears in New Mexico, and may be considered as future areas for research.

New Mexico

Anthropogenic impacts to the recovery of the Mexican gray wolf with a focus on trapping-related incidents

Concerns regarding the potential negative impacts of regulated furbearer trapping to reintroduced Mexican gray wolves (Canis lupus baileyi), led to an executive order prohibiting trapping in the New Mexico, USA, portion of the Blue Range Wolf Recovery Area. This ban was to last for 6 months and required an evaluation of the risk posed to wolves by traps and snares legally permitted in New Mexico. We reviewed potential threats to wolves in the Blue Range Wolf Recovery Area, including threats associated with regulated furbearer trapping. One hundred Mexican gray wolf mortalities have been documented during the reintroduction effort (1998–2011). Of those mortalities with a known cause, >81% were human-caused resulting from illegal shooting (n = 43), vehicle collisions (n = 14), lethal removal by the United States Fish and Wildlife Service (USFWS; n = 12), non-project-related trapping (n = 2), project-related trapping (n = 1), and legal shooting by the public (n = 1). Ten wolves died due to unknown causes. The remaining 17 mortalities were a result of natural causes (e.g., starvation, disease). An additional 23 wolves were permanently, but non-lethally, removed from the wild by the USFWS. Of 13 trapping incidents in New Mexico that involved non-project trappers (i.e., trappers not associated with USFWS or U.S. Department of Agriculture-Wildlife Services), 7 incidents are known to have resulted in injuries to wolves: 2 wolves sustained injuries severe enough to result in leg amputations and 2 additional wolves died as a result of injuries sustained. Foothold traps with rubber-padded jaws and properly set snares may reduce trap-related injuries to Mexican gray wolves; however, impacts caused by trapping are overshadowed by other anthropogenic impacts (e.g., illegal shooting, non-lethal permanent removal, and vehicle collisions).

New Mexico

Re-wilding North America

A plan to restore animals that disappeared 13,000 years ago from Pleistocene North America offers an alternative conservation strategy for the twenty-first century, argue Josh Donlan and colleagues.

Nature