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Odocoileus virginianus (white-tailed deer) and O. hemionus (mule deer) are sympatric across much of North America. Molecular evidence suggests that up to 24% of individuals in some populations are a product of hybrid ancestry. Several studies have alluded to ancient and recent introgression between Odocoileus spp.; however, no divergence dates were proposed. Herein, phylogenetic analyses of DNA sequences obtained from the mitochondrial Cytochrome b gene in 690 individuals identified three clades corresponding to black-tailed deer, white-tailed deer, or a unique combination of both white-tailed deer and mule deer. White-tailed deer and mule deer diverged from a common ancestor of approximately 3.13 mya followed by an ancient hybridization event of approximately 1.32 mya, in which the white-tailed deer mitochondrial genome was “captured” by mule deer. This hybridization event produced a novel haplogroup for white-tailed deer and mule deer located west of the Appalachian Mountains and east of the Cascade Range, south to Veracruz, Mexico, and north to the Yukon Territory, Canada. The ancestral mule deer-like mitochondrial genome appears to be restricted to black-tailed deer distributed along the western portion of the Cascade and Sierra Nevada Ranges of the United States and Canada, whereas the ancestral white-tailed deer-like mitochondrial genome is restricted to the eastern United States and portions of Latin America and Caribbean regions. The “captured mitochondrial genome” has continued on an independent evolutionary trajectory and represents a unique and broadly distributed haplogroup that is 7.25% and 2.84% different from the ancestral mule deer and ancestral white-tailed deer haplogroups, respectively. Odocoileus virginianus (ciervo de cola blanca) y O. hemionus (cievo mulo) son simpátricos a lo largo de Norte América. Evidencia molecular sugiere que en algunas poblaciones un 24% de individuos son el producto de linajes híbridos. Varios estudios aluden introgresiones antiguas y recientes entre Odocoileus spp. sin embargo, no proponen fecha de tal divergencia. En este estudio, los análisis filogenéticos de secuencias de ADN obtenidas del gen mitocondrial citocromo-b de 690 individuos, identificaron tres clados que corresponden al ciervo de cola negra, ciervo de cola blanca, o una combinación única de ciervo de cola blanca y ciervo mulo. El ciervo de cola blanca y el ciervo mulo divergieron de un ancestro común hace aproximadamente 2.65 Ma, seguido de un evento antiguo de hibridación hace aproximadamente 1.12 Ma en donde el genoma mitocondrial del ciervo de cola blanca fue “capturado” por el ciervo mulo. Este evento de hibridación produjo un nuevo haplogrupo en el ciervo de cola blanca y en el ciervo mulo localizados al Oeste de las Montañas Apalaches, al Este de las Cordilleras de Cascadas, al Sur de Veracruz, México, y al Norte del Territorio Yukón en Canadá. El genoma mitocondrial y ancestral semejante al ciervo mulo parece estar restringido al ciervo de cola negra que se distribuye a lo largo de la porción Oeste de las Cordilleras Sierras Nevadas y de la Cordillera de Cascadas de los EE. UU. y Canadá; mientras que, el genoma mitocondrial y ancestral semejante al ciervo de cola blanca se restringe al Este de los EE. UU. y partes de las regiones de Latinoamérica y el Caribe. El “genoma mitocondrial capturado” continuó una trayectoria evolutiva independiente y representa un único haplogrupo distribuido ampliamente siendo 7.25% y 2.84% diferente del haplogrupo del ancestro del ciervo mulo y del ancestro del ciervo de cola blanca respectivamente.

Tricholipeurus lipeuroides has previously been observed infesting mule deer and white-tailed deer in Alberta and British Columbia (Spencer 1939; Hopkins 1960; Russell 1967, Samuel et al. 1980; Colwell et al. 2008); T lipeuroides has also been reported infesting white-tailed deer in Manitoba (Galloway, unpublished data), Ontario (Scholten et al. 1962; Watson and Anderson 1975), and Quebec (Webster and Stewart 1964). Since the identification of T lipeuroides was confirmed, the examiners were able to collect more louse specimens. Evaluation of ivermectin for treatment of hair loss syndrome in black-tailed deer. First record of chewing lice, Damalinia (Tricholipeurus) lipeuroides and D. parallela (Phthiraptera: Trichodectidae), on white-tailed deer (Mammalia: Cervidae) in the U.S. Virgin Islands, with a review of other such introductions worldwide.

Individual‐ and species‐level heterogeneity in contact rates can alter the ability of a pathogen to invade a host community. Many pathogens have multiple modes of transmission—by direct or indirect contact. It is important to identify the role of heterogeneity in different types of transmission when managing the risk of disease spillover at the interface among different host species. We developed a network‐based analysis to explore how individual‐ and species‐level heterogeneity shape multi‐mode contact networks. We applied this network‐based approach to contact data from proximity loggers collected in a multi‐species host community that contributes to the spillover of the disease bovine tuberculosis (bTB) to cattle populations in Michigan, USA. We used this approach to (a) quantify how individual‐ and species‐level heterogeneity influence direct and indirect contacts in this system, (b) explore how management interventions to control spillovers, such as the installation of deer fences, can alter observed contact networks and c) predict the role that wildlife species have in maintaining bTB in the community. We found that individual‐ and species‐level heterogeneity disproportionately influenced indirect and direct contact networks, with individual‐level heterogeneity having a greater effect on indirect contact networks and species‐level heterogeneity having a greater effect on direct contact networks. We also found that the installation of deer fences significantly reduced deer‐specific indirect contacts. We used the results from our network analysis to show that white‐tailed deer (Odocoileus virginianus) could act as the sole reservoir host for bTB in this community with important implications for understanding past bTB dynamics and managing the persistence of bTB in the future. Synthesis and applications. Analyses of epidemiological networks rarely account for multiple modes of contact, which can lead to an incomplete understanding of how individual‐ and species‐level heterogeneity affect disease transmission. The multi‐mode, multi‐species network analysis we develop in this study illustrates that individual‐ and species‐level heterogeneity can play significantly different roles depending on the type of contact network considered. This has important implications when managing disease at the wildlife–livestock interface, where strategies may need to be multi‐pronged to account for the variable role of heterogeneity on different modes of contact. Analyses of epidemiological networks rarely account for multiple modes of contact, which can lead to an incomplete understanding of how individual‐ and species‐level heterogeneity affect disease transmission. The multi‐mode, multi‐species network analysis we develop in this study illustrates that individual‐ and species‐level heterogeneity can play significantly different roles depending on the type of contact network considered. This has important implications when managing disease at the wildlife–livestock interface, where strategies may need to be multi‐pronged to account for the variable role of heterogeneity on different modes of contact.

Camera trapping is a powerful tool for studying mammal populations over large spatial scales. Density estimation using camera-trap data is a commonly desired outcome, but most approaches only work for species that can be individually recognized, and researchers studying most mammals are typically constrained to measures of site occupancy or detection rate. These 2 metrics are often used as measures of relative abundance and presumed to be related directly to animal density. To test this relationship, we estimated density, occupancy, and detection rate of male white-tailed deer (Odocoileus virginianus) using camera-trap data collected from 1,199 cameras across 20 study sites. Detection rate and density exhibited stronger positive linear correlation (r2 = 0.80) than occupancy and density (r2 = 0.27). When hunted and unhunted paired areas were compared, detection rate and density showed the same trend between paired sites 62.5% of the time compared to 87.5% for occupancy and density. In particular, agreement between estimates was lowest for pairs of sites that had the largest differences in surrounding housing density. Although it is clear occupancy and detection rate contain some information about density, models suggested different ecological relationships associated with the metrics. Using occupancy or detection rate as proxies for density may be particularly problematic when comparing between areas where animals might to move or behave differently, such as urban–wild interfaces. In such cases, alternate methods of density approximation are recommended.

Chronic wasting disease (CWD) is a fatal transmissible spongiform encephalopathy affecting white-tailed deer (Odocoileus virginianus), mule deer (Odocoileus hemionus), Rocky Mountain elk (Cervus elaphus nelsoni), and moose (Alces alces shirasi) in North America. In southeastern Wyoming average annual CWD prevalence in mule deer exceeds 20% and appears to contribute to regional population declines. We determined the effect of CWD on mule deer demography using age-specific, female-only, CWD transition matrix models to estimate the population growth rate (λ). Mule deer were captured from 2010-2014 in southern Converse County Wyoming, USA. Captured adult (≥ 1.5 years old) deer were tested ante-mortem for CWD using tonsil biopsies and monitored using radio telemetry. Mean annual survival rates of CWD-negative and CWD-positive deer were 0.76 and 0.32, respectively. Pregnancy and fawn recruitment were not observed to be influenced by CWD. We estimated λ = 0.79, indicating an annual population decline of 21% under current CWD prevalence levels. A model derived from the demography of only CWD-negative individuals yielded; λ = 1.00, indicating a stable population if CWD were absent. These findings support CWD as a significant contributor to mule deer population decline. Chronic wasting disease is difficult or impossible to eradicate with current tools, given significant environmental contamination, and at present our best recommendation for control of this disease is to minimize spread to new areas and naïve cervid populations.

For decades, mule deer Odocoileus hemionus populations have appeared to shrink across their range in North America, while white‐tailed deer O. virginianus populations have increased, and their range has expanded. The underlying drivers of these patterns are unclear, and a combination of factors may be at play, including land use changes, climate change, and direct or indirect competition between the two species. Understanding how the two species differentially use the landscape and select habitat would help shed light on the underlying drivers of mule deer decline and highlight opportunities to change population trajectories through habitat management. Using an extensive GPS dataset on mule deer (n = 345) and white‐tailed deer (n = 345) in their sympatric range, we used resource selection functions to investigate the relative probability of selection of different resources available to the two species. We estimated population‐level relative probability of selection in winter and summer and demonstrated that a combination of factors, including nutrition, thermal cover, and human impact described resource selection better than any single factor on its own, despite annual variation in these metrics. In keeping with long‐established patterns, we verified that white‐tailed deer had more consistent selection than mule deer for agriculture, higher human modification, road density and tree cover. Across seasons and years, individuals of both species consistently selected for shrubs, perennial forbs and grasses, and steeper slopes. Using our large dataset, we performed out‐of‐sample validation and demonstrated that although the resource selection functions predicted space use well at the population level, they performed poorly at predicting resource selection between individuals or even within an individual over time. Thus, while we successfully identified key habitat characteristics that were selected differentially by individuals from the two deer species, inferring individual habitat selection and future resource use patterns proved challenging.

1. In forests of eastern North America, white-tailed deer (Odocoileus virginianus) can directly affect, via herbivory, the presence, abundance and reproductive success of many plant species. In addition, deer indirectly influence understorey communities by altering environmental conditions. 2. To examine how deer indirectly influence understorey plants via environmental modification, we sampled vegetation and environmental variables in- and outside deer exclosures (10-20 years old) located in temperate forests in northern Wisconsin and the Upper Peninsula of Michigan, USA. We assessed how excluding deer affected understorey community composition and structure, the soil and light environment, and relationships between direct and indirect effects, using non-metric multidimensional scaling (NMDS), mixed linear models and nonparametric multiplicative regression (NPMR). 3. Excluding deer altered sapling communities and several aspects of the understorey environment. Excluding deer from plots with lower overstory basal area increased sapling abundance, decreasing the amount of light available to groundlayer plants. Exclusion also reduced soil compaction and the thickness of the soil E horizon. 4. The composition of understorey communities covaried in apparent response to the environmental factors affected by exclusion. In several common species and groups, E horizon thickness, compaction, openness, and/or total (sapling and overstory) basal area were significant predictors of plant frequency. 5. Complementary analyses revealed that deer exclusion also altered the frequency distributions of several species and groups across environmental space. 6. Synthesis. Deer alter many facets of the understorey environment, such as light availability, soil compaction and thickness of the soil E horizon, which, in turn, appear to mediate variation in plant communities. Those environmental modifications likely compound direct impacts of herbivory as drivers of understorey community change. Our results provide evidence that deer effects on the environment have important implications for forest composition. Thus, we suggest a re-examination of the common assumption that understorey community shifts stem primarily from tissue removal.

Widespread human SARS-CoV-2 infections combined with human–wildlife interactions create the potential for reverse zoonosis from humans to wildlife. We targeted white-tailed deer (Odocoileus virginianus) for serosurveillance based on evidence these deer have angiotensin-converting enzyme 2 receptors with high affinity for SARS-CoV-2, are permissive to infection, exhibit sustained viral shedding, can transmit to conspecifics, exhibit social behavior, and can be abundant near urban centers. We evaluated 624 prepandemic and postpandemic serum samples from wild deer from four US states for SARS-CoV-2 exposure. Antibodies were detected in 152 samples (40%) from 2021 using a surrogate virus neutralization test. A subset of samples tested with a SARS-CoV-2 virus neutralization test showed high concordance between tests. These data suggest white-tailed deer in the populations assessed have been exposed to SARS-CoV-2.

The availability and quality of forage on the landscape constitute the foodscape within which animals make behavioral decisions to acquire food. Novel changes to the foodscape, such as human disturbance, can alter behavioral decisions that favor avoidance of perceived risk over food acquisition. Although behavioral changes and population declines often coincide with the introduction of human disturbance, the link(s) between behavior and population trajectory are difficult to elucidate. To identify a pathway by which human disturbance may affect ungulate populations, we tested the Behaviorally Mediated Forage-Loss Hypothesis, wherein behavioral avoidance is predicted to reduce use of available forage adjacent to disturbance. We used GPS collar data collected from migratory mule deer (Odocoileus hemionus) to evaluate habitat selection, movement patterns, and time-budgeting behavior in response to varying levels of forage availability and human disturbance in three different populations exposed to a gradient of energy development. Subsequently, we linked animal behavior with measured use of forage relative to human disturbance, forage availability, and quality. Mule deer avoided human disturbance at both home range and winter range scales, but showed negligible differences in vigilance rates at the site level. Use of the primary winter forage, sagebrush (Artemisia tridentata), increased as production of new annual growth increased but use decreased with proximity to disturbance. Consequently, avoidance of human disturbance prompted loss of otherwise available forage, resulting in indirect habitat loss that was 4.6-times greater than direct habitat loss from roads, well pads, and other infrastructure. The multiplicative effects of indirect habitat loss, as mediated by behavior, impaired use of the foodscape by reducing the amount of available forage for mule deer, a consequence of which may be winter ranges that support fewer animals than they did before development.

Abstract The glacial cycles of the Quaternary heavily impacted species through successions of population contractions and expansions. Similarly, populations have been intensely shaped by human pressures such as unregulated hunting and land use changes. White-tailed and mule deer survived in different refugia through the Last Glacial Maximum, and their populations were severely reduced after the European colonization. Here, we analyzed 73 resequenced deer genomes from across their North American range to understand the consequences of climatic and anthropogenic pressures on deer demographic and adaptive history. We found strong signals of climate-induced vicariance and demographic decline; notably, multiple sequentially Markovian coalescent recovers a severe decline in mainland white-tailed deer effective population size (Ne) at the end of the Last Glacial Maximum. We found robust evidence for colonial overharvest in the form of a recent and dramatic drop in Ne in all analyzed populations. Historical census size and restocking data show a clear parallel to historical Ne estimates, and temporal Ne/Nc ratio shows patterns of conservation concern for mule deer. Signatures of selection highlight genes related to temperature, including a cold receptor previously highlighted in woolly mammoth. We also detected immune genes that we surmise reflect the changing land use patterns in North America. Our study provides a detailed picture of anthropogenic and climatic-induced decline in deer diversity and clues to understanding the conservation concerns of mule deer and the successful demographic recovery of white-tailed deer.