Condensed Tannins' Effect on White-Tailed Deer Forage Digestibility in Mississippi

Abstract: Condensed tannins (CT) can reduce digestibility of forages for white-tailed deer (Odocoileus virginianus), potentially confounding estimates of diet quality and nutritional carrying capacity. We collected 143 spring and 142 summer samples of 8 important deer forage species from 22 properties in Mississippi, USA, and tested for CT content using a modified butanol-HCl assay. Three species (partridge pea [Chamaecrista fasciculata], southern dewberry [Rubus trivialis], and roundleaf greenbrier [Smilax rotundifolia]) contained CT, ranging from 0.11% to 6.46% dry weight. Summer CT concentration was greater than in spring for 2 species. We ranked soil samples from least to most fertile using 8 chemical characteristics and found a positive correlation between fertility and CT concentration for 1 species and no correlation for 2 species. We tested effects of CT concentration on in vitro dry matter disappearance (IVDMD) and in vitro protein digestibility using samples of partridge pea and roundleaf greenbrier and rumen fluid from 3 free-ranging deer. Average IVDMD was reduced 1.9% for each 1% increase in CT concentration. In vitro protein digestibility was reduced 2.5% for each 1% increase in CT concentration. Assuming that our methods reflect the effects of CT on in vivo digestibility, maximum loss of available crude protein (CP) in our samples was 3.0 g/100 g dry-weight forage, and only 13 of the 112 CT-containing forage samples (12%) would have decreased available CP by >1 g/100 g dry-weight forage. Deer consuming equal portions of sampled forages would lose <1% of dietary CP to CT. Comparisons of foraging area quality using crude protein estimates should be unaffected by CT under reasonable restrictions of similar habitat types, soil fertility, and time. Given the ability of deer to forage selectively and the abundance of alternative forages in Mississippi, the potential for CT to substantially affect spring or summer diet quality of deer appears minimal.     

Cougar Prey Selection in a White-Tailed Deer and Mule Deer Community

Abstract Widespread mule deer (Odocoilus hemionous) declines coupled with white-tailed deer (O. virginianus) increases prompted us to investigate the role of cougar (Puma concolor) predation in a white-tailed deer, mule deer, and cougar community in northeast Washington, USA. We hypothesized that cougars select for and disproportionately prey on mule deer in such multiple-prey communities. We estimated relative annual and seasonal prey abundance (prey availability) and documented 60 cougar kills (prey usage) from 2002 to 2004. White-tailed deer and mule deer comprised 72% and 28% of the total large prey population and 60% and 40% of the total large prey killed, respectively. Cougars selected for mule deer on an annual basis (α_md = 0.63 vs. α_wt = 0.37; P = 0.066). We also detected strong seasonal selection for mule deer with cougars killing more mule deer in summer (α_md = 0.64) but not in winter (α_md = 0.53). Cougars showed no seasonal selection for white-tailed deer despite their higher relative abundance. The mean annual kill interval of 6.68 days between kills varied little by season (winter = 7.0 days/kill, summer = 6.6 days/kill; P = 0.78) or prey species (white-tailed deer = 7.0 days/kill, mule deer = 6.1 days/kill; P = 0.58). Kill locations for both prey species occurred at higher elevations during summer months (summer = 1,090 m, winter = 908 m; P = 0.066). We suspect that cougars are primarily subsisting on abundant white-tailed deer during winter but following these deer to higher elevations as they migrate to their summer ranges, resulting in a greater spatial overlap between cougars and mule deer and disproportionate predation on mule deer.     

Integrated Population Modeling for White-Tailed Deer in Saskatchewan,Canada

Monitoring annual change and long-term trends in population structure and abundance of white-tailed deer (Odocoileus virginianus) is an important but challenging component of their management. Many monitoring programs consist of count-based indices of relative abundance along with a variety of population structure information. Analyzed separately these data can be difficult to interpret because of observation error in the data collection process, missing data, and the lack of an explicit biological model to connect the data streams while accounting for their relative imprecision. We used a Bayesian age-structured integrated population model to integrate data from a fall spotlight survey that produced a count-based index of relative abundance and a volunteer staff and citizen classification survey that generated a fall recruitment index. Both surveys took place from 2003–2018 in the parkland ecoregion of southeast Saskatchewan, Canada. Our approach modeled demographic processes for age-specific (0.5-, 1.5-, ≥2.5-year-old classes) populations and was fit to count and recruitment data via models that allowed for error in the respective observation processes. The Bayesian framework accommodated missing data and allowed aggregation of transects to act as samples from the larger management unit population. The approach provides managers with continuous time series of estimated relative abundance, recruitment rates, and apparent survival rates with full propagation of uncertainty and sharing of information among transects. We used this model to demonstrate winter severity effects on recruitment rates via an interaction between winter snow depth and minimum temperatures. In years with colder than average temperatures and above average snow depth, recruitment was depressed, whereas the negative effect of snow depth reversed in years with above average temperatures. This and other covariate information can be incorporated into the model to test relationships and provide predictions of future population change prior to setting of hunting seasons. Likewise, post hoc analysis of model output allows other hypothesis tests, such as determining the statistical support for whether population status has crossed a management trigger threshold. © 2020 The Wildlife Society.     

Reduction and Maintenance of a White-Tailed Deer Herd in Central Massachusetts

Abstract: Controlled public hunts have been used in a variety of settings to reduce overabundant white-tailed deer (Odocoileus virginianus) herds. We present the results of a large-scale (160 km²) controlled hunt at Quabbin Reservation (QR) in central Massachusetts, USA. The QR was divided into 5 hunt zones. Hunting was initiated in each zone from 1991 to 1994 and continued through 2004. The management goal was to achieve posthunt deer densities of4 deer/km². Initial estimated deer densities in each zone ranged from 11.4 deer/km² to 27.6 deer/km². The management goals were reached in each zone after 2-4 years of hunting. Posthunt populations were maintained at or below the goal even though total hunter effort was reduced. Hunters were not required to harvest antlerless deer, but antlerless deer comprised 55-83% of the harvest each year. We simulated the effects of 5 years without hunting on deer populations. The simulated deer population exceeded management goals after 2 years. Our results demonstrate that controlled public deer hunts can effectively reduce deer populations and maintain them at desired levels over large areas with minimal hunter restrictions. Managers should prepare stakeholders during the hunt planning process for the need to continue overall harvest rates of >30% during the maintenance phase of a deer management program.     

White-Tailed Deer,Weather and Predation: a New Understanding of Winter Severity for Predicting Deer Mortality

Variation in white-tailed deer (Odocoileus virginianus) mortality during winter affects population growth in cold climates. Across the northern extent of their range, mortality increases with colder temperatures and snow. Few studies have examined the relationships between winter conditions and deer mortality, and no studies have concurrently studied this relationship for different ages of deer across multiple years and landscapes. We used recently developed cause-specific mortality models to evaluate temporal and age-class variation in deer mortality in farmland areas and compared to published results from forest areas in Wisconsin, USA, from 2011–2014. We then used temporally varying snow and temperature covariates to predict mortality trends using telemetry information from 860 deer. Cause-specific mortality in the farmland varied by age and year, similar to results from previous research in the forest. Human-related mortality was the leading cause of mortality in the farmland during most years and ranged from 4.3% to 10.3% for juveniles and 3.6% to 9.1% for adults from 2011–2014. Very little predation occurred in the farmland, and this differed from previous research in the forest where predation was the leading cause of mortality. During more severe winters (2013 and 2014), other mortality, usually associated with starvation, was the leading cause of mortality for juveniles in the farmland but not adults. In the forest, we found support for saturating effects of accumulated snow depth days >30.5 cm and accumulated temperature days >0°C on mortality. We also found support for the relationship of mortality with accumulated temperature days >0°C in the farmland but no relationship with snow depth. Deer tolerate sustained cold temperatures, but the timing of winter to spring transition is more important for deer survival in both forested and agricultural areas. In the absence of empirical survival information, managers can use our model to predict annual winter effects on deer survival, which can provide improved inference compared to traditional winter severity indices. Our results suggest changes in predator abundance may have minor influence on overwinter survival compared to winter weather. Based on mortality estimates from previous research, the highest predation rates on juvenile deer in the forest occurred when wolf (Canis lupus) counts were lowest and when wolf abundance was highest, juvenile deer predation rates were lowest. © 2021 The Wildlife Society.     

Evaluation of Shifts in White-Tailed Deer Winter Yards in the Adirondack Region of New York

ABSTRACT In the Adirondack region of northern New York, USA, severe weather and deep snow typically force white-tailed deer (Odocoileus virginianus) to congregate in areas of dense coniferous cover and along watercourses at lower elevations. We examined 16 yards in the Adirondacks and explored the observation that deer have changed their movement behavior to incorporate residential communities within their wintering areas. We compared locations of deer herds in 2003 and 2004 to deer wintering areas mapped during the 1960s and 1970s. Deer were predominantly absent in 9 of 16 historical yards but were present in residential communities within the same drainage. Yarding areas to which deer shifted contained more residential, deciduous, and mixed cover than yards where no shift occurred, indicating that deer in residential areas were using conifer and mixed cover at a finer scale than deer in nonresidential areas. Smaller winter ranges and core areas of marked deer in a residential winter yard further imply greater concentration of resources available in these areas. Marked deer demonstrated flexibility in core winter range fidelity, a behavior that allows for more permanent shifts as habitat and food resources change or as new areas with appropriate resources are encountered. Our study suggests that low-density residential areas in lowland conifer forests may provide an energetic advantage for deer during winter due to the assemblage of quality habitat interspersed with open areas and a variety of potential food sources in environments where movement is typically constrained by deep snow. Managers should consider the potential for changes in use of deer wintering areas prior to land conservation efforts and may need to adapt management strategies to reduce conflicts in communities occupied by deer during winter.     

Evaluating the Mechanisms of Landscape Change on White-Tailed Deer Populations

Understanding how landscape change influences the distribution and densities of species, and the consequences of these changes, is a central question in modern ecology. The distribution of white-tailed deer (Odocoileus virginianus) is expanding across North America, and in some areas, this pattern has led to an increase in predators and consequently higher predation rates on woodland caribou (Rangifer tarandus caribou)—an alternate prey species that is declining across western Canada. Understanding the factors influencing deer distribution has therefore become important for effective conservation of caribou in Canada. Changing climate and anthropogenic landscape alteration are hypothesized to facilitate white-tailed deer expansion. Yet, climate and habitat alteration are spatiotemporally correlated, making these factors difficult to isolate. Our study evaluates the relative effects of snow conditions and human-modified habitat (habitat alteration) across space on white-tailed deer presence and relative density. We modeled deer response to snow depth and anthropogenic habitat alteration across a large latitudinal gradient (49° to 60°) in Alberta, Canada, using motion-sensitive camera data collected in winter and spring from 2015 to 2019. Deer distribution in winter and spring were best explained by models including both snow depth and habitat alteration. Sites with shallower snow had higher deer presence regardless of latitude. Increased habitat alteration increased deer presence in the northern portion of the study area only. Winter deer density was best explained by snow depth only, whereas spring density was best explained by both habitat alteration and the previous winter's snow depth. Our results suggest that limiting future habitat alteration or restoring habitat can alter deer distribution, thereby potentially slowing or reversing expansion, but that climate plays a significant role beyond what managers can influence. © 2020 The Wildlife Society.     

Survival,Birth Characteristics,and Cause-Specific Mortality of White-Tailed Deer Neonates

ABSTRACT Understanding survival of and factors that may predispose newborn deer (Odocoileus spp.) to mortality contribute to improved understanding of population dynamics. We captured free-ranging white-tailed deer neonates (n = 66) of radiocollared females that survived severe (Winter Severity Index [WSI] = 153) and mild (WSI = 45) winters 2000–2001 and 2001–2002. Mean dates of birth (26 May ± 1.7 [SE] days and 26 May ± 1.3 days) and estimated birth-masses of 2.8 ± 0.1 kg and 3.0 ± 0.1 kg were similar between springs 2001 (n = 31) and 2002 (n = 35), respectively. Neonate survival was similar between years; pooled mortality rates of neonates were 0.14, 0.11, and 0.20 at 0–1 weeks, 2–4 weeks, and 5–12 weeks of age, respectively, and overall survival rate for neonates to 12 weeks of age was 0.47. Predation accounted for 86% of mortality; the remaining 14% of deaths were attributed to unknown causes. Black bears (Ursus americanus) were responsible for 57% and 38% of predation of neonates in springs 2001 and 2002, respectively, whereas bobcats (Felis rufus) accounted for 50% in 2002. Wolves (Canis lupus) accounted for only 5% of predator-related deaths. Low birth-mass, smaller body size, and elevated concentrations of serum urea nitrogen (26.1 ± 2.6 mg/dL vs 19.3 ± 0.8 mg/dL) and tumor necrosis factor-α (82.6 ± 78.6 pg/mL vs. 2.3 ± 0.5 pg/mL) were associated with neonates that died within 1 week of birth. Even though we did not detect a direct relation between winter severity and birth or blood characteristics of neonates, evidence suggests that birth-mass and key serum indices of neonate nutrition were associated with their early mortality. Thus, managers can make more informed predictions regarding survival and cause-specific mortality of fawns and adjust management strategies to better control deer population goals.     

Effects of Maternal Status on the Movement and Mortality of Sterilized Female White-Tailed Deer

Abstract: Surgical sterilization by tubal ligation has been proposed as a technique for controlling white-tailed deer (Odocoileus virginianus) populations in urban or suburban areas where other forms of population control are impractical, but little is known about demographic rates in populations under management with surgical sterilization. We analyzed seasonal movement and mortality data collected during a 4-year study of surgical sterilization in suburban Chicago, Illinois, USA. We calculated 323 home range size estimates for 62 individual females within season and year. Non-gravid females without young exhibited home range sizes 52% larger than gravid females and females with fawns. Mortality rate was positively correlated with home range size. We suggest that the increased mortality rate observed in surgically sterilized females may be due to greater movement by non-maternal females. Population managers will need to account for potential effects of maternal status on movement and mortality when considering the use of sterilization for management of suburban populations of white-tailed deer.     

White-Tailed Deer Movements in a Chronic Wasting Disease Area in South-Central Wisconsin

Abstract: To focus white-tailed deer (Odocoileus virginianus) management within a chronic wasting disease-infected area in south-central Wisconsin, USA, we assessed deer movements and related dispersal to variation in landscape pattern, deer density, and harvest intensity. We radiocollared and monitored 165 deer between 2003 and 2005. Yearling males that dispersed (45%) had greater forest edge (i.e., fragmentation) within natal home ranges. Exploratory movements were rare for adult females. Transient and migratory movements were rare among all deer (<5%). Although yearling males have low chronic wasting disease prevalence rates, they may be infected before dispersal due to variable incubation times. Managers should increase yearling male harvest and consider removing young males in areas of higher forest edge.     

Linking alternative food sources to winter habitat selection of herbivores in overbrowsed landscapes

During winter, ungulates in boreal forests must cope with high energetic costs related to locomotion in deep snow and reduced forage abundance and quality. At high density, ungulates face additional constraints, because heavy browsing reduces availability of woody browse, the main source of forage during winter. Under these severe conditions, large herbivores might forage on alternative food sources likely independent of browsing pressure, such as litterfall or windblown trees. We investigated the influence of alternative food sources on winter habitat selection, by studying female white-tailed deer (Odocoileus virginianus) living in 2 landscapes with contrasted browse abundance, recently logged and regenerated landscapes, in a population at high density and on a large island free of predators. We fitted 21 female white-tailed deer with Global Positioning System (GPS) collars and delineated winter home ranges and core areas. We measured snow conditions in different habitat categories and sampled vegetation in the core areas and in the rest of the home ranges to determine how forage abundance, protective cover, and snow conditions influenced habitat selection within the home range. In both landscapes, deer were less likely to use open habitat categories as snow accumulated on the ground. At a finer scale, deer inhabiting the regenerated landscape intensively used areas where balsam fir cover was intermediate with greater balsam fir browse density than in the rest of the home range. In the recently logged landscape, deer were more likely to be found near edges between clear-cuts and balsam fir stands and in areas where windblown balsam fir trees were present; the latter being the most influential variable. Although balsam fir browse was sparse and mainly out of reach in this landscape, deer increased the use of areas where it was present. Our results offer novel insights into the resource selection processes of northern ungulates, as we showed that access to winter forage, such as woody browse and alternative food sources, depends on climatic conditions and stochastic events, such as abundant compacted snow or windthrows. To compensate for these scarce and unpredictable food supplies, deer selected habitat categories, but mostly areas within those habitat categories, where the likelihood of finding browse, litterfall, and windblown trees was greatest. © 2011 The Wildlife Society.     

Detection Probability and Sources of Variation in White-Tailed Deer Spotlight Surveys

Abstract: As a first step in understanding structure and dynamics of white-tailed deer (Odocoileus virginianus) populations, managers require knowledge of population size. Spotlight counts are widely used to index deer abundance; however, detection probabilities using spotlights have not been formally estimated. Using a closed mark—recapture design, we explored the efficiency of spotlights for detecting deer by operating thermal imagers and spotlights simultaneously. Spotlights detected only 50.6% of the deer detected by thermal imagers. Relative to the thermal imager, spotlights failed to detect 44.2% of deer groups (≥1 deer). Detection probabilities for spotlight observers varied between and within observers, ranging from 0.30 (SE = 0.053) to 0.66 (SE = 0.058). Managers commonly assume that although road counts based on convenience sampling designs are imperfect, observers can gather population-trend information from repeated counts along the same survey route. Our results indicate detection rate varied between and within observers and surveyed transects. If detection probabilities are substantially affected by many variables, and if transect selection is not based on appropriate sampling designs, it may be impractical to correct road spotlight counts for detection probabilities to garner unbiased estimates of population size.     

Diets,Movements, and Consequences of Providing Wildlife Food Plots for White-Tailed Deer in Central North Dakota

ABSTRACT White-tailed deer (Odocoileus virginianus) in North Dakota, USA, have greatly increased over the past 100 years due to conversion of prairie to agriculture, planting of tree rows, regulated hunting, and extirpation of large predators. In support of management to maintain harvestable big game while minimizing depredation damage to agriculture, the North Dakota Game and Fish Department manages wildlife management areas (WMAs) where planted trees and food plots provide habitat and public hunting. These WMAs are typically surrounded by agricultural fields, and management that concentrates deer in these areas may expose surrounding agricultural producers to increased depredation. We investigated diets, habitat use, and movements of white-tailed deer at a large WMA in central North Dakota (Lonetree WMA) to understand how the animals are responding to management designed to enhance wildlife populations. We also evaluated survival of white-tailed deer for an improved understanding of the recent trend for population growth. Diets of deer varied seasonally, including a relatively high proportion of crops from food plots in winter and mostly herbaceous forbs and browse during spring and summer. Data from radiocollared animals and biweekly spotlight surveys revealed that deer are being drawn from a relatively large area to Lonetree WMA during fall and winter. Hunting was the most important cause of mortality, but annual survival of adult and fawn females exceeded 80%. The original purpose of food plots at Lonetree WMA was to alleviate depredation on adjacent private lands. Depredation has been limited, but the multiyear trend of increased deer numbers is a new concern. A possible consequence of provisioning white-tailed deer with food plots during winter when some starvation would normally occur could be for the population to exceed a threshold above which regulated hunting will be unable to prevent irruptive growth. Research on how food plots influence winter survival is needed to inform management and prevent possible rapid increase in white-tailed deer populations across the prairie-coteau region of central North Dakota.     

Linking White-Tailed Deer Density,Nutrition, and Vegetation in a Stochastic Environment

Density-dependent behavior underpins white-tailed deer (Odocoileus virginianus) theory and management application in North America, but strength or frequency of the phenomenon has varied across the geographic range of the species. The modifying effect of stochastic environments and poor-quality habitats on density-dependent behavior has been recognized for ungulate populations around the world, including white-tailed deer populations in South Texas, USA. Despite the importance of understanding mechanisms influencing density dependence, researchers have concentrated on demographic and morphological implications of deer density. Researchers have not focused on linking vegetation dynamics, nutrition, and deer dynamics. We conducted a series of designed experiments during 2004–2012 to determine how strongly white-tailed deer density, vegetation composition, and deer nutrition (natural and supplemented) are linked in a semi-arid environment where the coefficient of variation of annual precipitation exceeds 30%. We replicated our study on 2 sites with thornshrub vegetation in Dimmit County, Texas. During late 2003, we constructed 6 81-ha enclosures surrounded by 2.4-m-tall woven wire fence on each study site. The experimental design included 2 nutrition treatments and 3 deer densities in a factorial array, with study sites as blocks. Abundance targets for low, medium, and high deer densities in enclosures were 10 deer (equivalent to 13 deer/km²), 25 deer (31 deer/km²), and 40 deer (50 deer/km²), respectively. Each study site had 2 enclosures with each deer density. We provided deer in 1 enclosure at each density with a high-quality pelleted supplement ad libitum, which we termed enhanced nutrition; deer in the other enclosure at each density had access to natural nutrition from the vegetation. We conducted camera surveys of deer in each enclosure twice per year and added or removed deer as needed to approximate the target densities. We maintained >50% of deer ear-tagged for individual recognition. We maintained adult sex ratios of 1:1–1:1.5 (males:females) and a mix of young and older deer in enclosures. We used reconstruction, validated by comparison to known number of adult males, to make annual estimates of density for each enclosure in analysis of treatment effects. We explored the effect of deer density on diet composition, diet quality, and intake rate of tractable female deer released into low- and high-density enclosures with natural nutrition on both study sites (4 total enclosures) between June 2009 and May 2011, 5 years after we established density treatments in enclosures. We used the bite count technique and followed 2–3 tractable deer/enclosure during foraging bouts across 4 seasons. Proportion of shrubs, forbs, mast, cacti, and subshrubs in deer diets did not differ (P > 0.57) between deer density treatments. Percent grass in deer diets was higher (P = 0.05) at high deer density but composed only 1.3 ± 0.3% (SE) of the diet. Digestible protein and metabolizable energy of diets were similar (P > 0.45) between deer density treatments. Likewise, bite rate, bite size, and dry matter intake did not vary (P > 0.45) with deer density. Unlike deer density, drought had dramatic (P ≤ 0.10) effects on foraging of tractable deer. During drought conditions, the proportion of shrubs and flowers increased in deer diets, whereas forbs declined. Digestible protein was 31%, 53%, and 54% greater (P = 0.06) during non-drought than drought during autumn, winter, and spring, respectively. We studied the effects of enhanced nutrition on the composition and quality of tractable female deer diets between April 2007 and February 2009, 3 years after we established density treatments in enclosures. We also estimated the proportion of supplemental feed in deer diets. We used the 2 low-density enclosures on each study site, 1 with enhanced nutrition and 1 with natural nutrition (4 total enclosures). We again used the bite count technique and 2–3 tractable deer living in each enclosure. We estimated proportion of pelleted feed in diets of tractable deer and non-tractable deer using ratios of stable isotopes of carbon. Averaged across seasons and nutrition treatments, shrubs composed a majority of the vegetation portion of deer diets (44%), followed by mast (26%) and forbs (15%). Enhanced nutrition influenced the proportion of mast, cacti, and flowers in the diet, but the nature and magnitude of the effect varied by season and year. The trend was for deer in natural-nutrition enclosures to eat more mast. We did not detect a statistical difference (P = 0.15) in the proportion of shrubs in diets between natural and enhanced nutrition, but deer with enhanced nutrition consumed 7–24% more shrubs in 5 of 8 seasons. Deer in enhanced-nutrition enclosures had greater (P = 0.03) digestible protein in their overall diet than deer in natural-nutrition enclosures. The effect of enhanced nutrition on metabolizable energy in overall diets varied by season and was greater (P < 0.04) for enhanced-nutrition deer during summer and autumn 2007 and winter 2008. In the enhanced-nutrition treatment, supplemental feed averaged 47–80% of the diet of tractable deer. Of non-tractable deer in all density treatments with enhanced nutrition, 97% (n = 128 deer) ate supplemental feed. For non-tractable deer averaged across density treatments, study sites, and years, percent supplemental feed in deer diets exceeded 70% for all sex and age groups. We determined if increasing deer density and enhanced nutrition resulted in a decline in preferred forbs and shrubs and an increase in plants less preferred by deer. We sampled all 12 enclosures via 20, 50-m permanent transects in each enclosure. Percent canopy cover of preferred forbs was similar (P = 0.13) among deer densities averaged across nutrition treatments and sampling years (low density: = 8%, SE range 6–10; medium density: 5%, 4–6; high density: 4%, 3–5; SE ranges are presented because SEs associated with backtransformed means are asymetrical). Averaged across deer densities, preferred forb canopy cover was similar between nutrition treatments in 2004; but by 2012 averaged 20 ± 17–23% in enhanced-nutrition enclosures compared to 10 ± 8–13% in natural-nutrition enclosures (P = 0.107). Percent canopy cover of other forbs, preferred shrubs, other shrubs, and grasses, as well as Shannon's index, evenness, and species richness were similar (P > 0.10) among deer densities, averaged across nutrition treatments and sampling years. We analyzed fawn:adult female ratios, growth rates of fawns and yearlings, and survival from 6 to 14 months of age and for adults >14 months of age. We assessed adult body mass and population growth rates (lambda apparent, λ_APP) to determine density and nutrition effects on deer populations in the research enclosures during 2004–2012. Fawn:adult female ratios declined (P = 0.04) from low-medium density to high density in natural-nutrition enclosures but were not affected (P = 0.48) by density in enhanced nutrition enclosures although, compared to natural nutrition, enhanced nutrition increased fawn:adult female ratios by 0.15 ± 0.12 fawns:adult female at low-medium density and 0.44 ± 0.17 fawns:adult female at high density. Growth rate of fawns was not affected by deer density under natural or enhanced nutrition (P > 0.17) but increased 0.03 ± 0.01 kg/day in enhanced-nutrition enclosures compared to natural nutrition (P < 0.01). Growth rate of yearlings was unaffected (P > 0.71) by deer density, but growth rate increased for males in some years at some density levels in enhanced-nutrition enclosures. Adult body mass declined in response to increasing deer density in natural-nutrition enclosures for both adult males (P < 0.01) and females (P = 0.10). Enhanced nutrition increased male body mass, but female mass did not increase compared to natural nutrition. Survival of adult males was unaffected by deer density in natural- (P = 0.59) or enhanced- (P = 0.94) nutrition enclosures. Survival of adult females was greatest in medium-density enclosures with natural nutrition but similar at low and high density (P = 0.04). Enhanced nutrition increased survival of females (P < 0.01) and marginally for males (P = 0.11). Survival of fawns 6–14 months old was unaffected (P > 0.35) by density in either natural- or enhanced-nutrition treatments but was greater (P = 0.04) under enhanced nutrition. Population growth rate declined (P = 0.06) with increasing density in natural-nutrition enclosures but not (P = 0.55) in enhanced nutrition. Enhanced nutrition increased λ_APP by 0.32. Under natural nutrition, we found only minor effects of deer density treatments on deer diet composition, nutritional intake, and plant communities. However, we found density-dependent effects on fawn:adult female ratios, adult body mass, and population growth rate. In a follow-up study, deer home ranges in our research enclosures declined with increasing deer density. We hypothesized that habitat quality varied among home ranges and contributed to density-dependent responses. Variable precipitation had a greater influence on deer diets, vegetation composition, and population parameters than did deer density. Also, resistance to herbivory and low forage quality of the thornshrub vegetation of our study sites likely constrained density-dependent behavior by deer. We posit that it is unlikely that, at our high-density (50 deer/km²) and perhaps even medium-density (31 deer/km²) levels, negative density dependence would occur without several wet years in close association. In the past century, this phenomenon has only happened once (1970s). Thus, density dependence would likely be difficult to detect in most years under natural nutrition in this region. Foraging by deer with enhanced nutrition did not result in a reduction in preferred plants in the vegetation community and had a protective effect on preferred forbs because ≤53% of deer diets consisted of vegetation. However, enhanced nutrition improved fitness of individual deer and deer populations, clearly demonstrating that nutrition is limiting for deer populations under natural conditions in western South Texas. © 2019 The Authors. Wildlife Monographs published by Wiley Periodicals, Inc. on behalf of The Wildlife Society.     

Spatial ecology of white-tailed deer fawns in the northern Great Plains: Implications of loss of conservation reserve program grasslands

Few studies have evaluated how wildlife, and white-tailed deer (Odocoileus virginianus) in particular, respond to Conservation Reserve Program (CRP) grasslands. We conducted a 3-year study (2007–2009) to determine the influence of CRP on fawn ecology during a time of declining CRP enrollment. We captured and radiocollared 81 fawn white-tailed deer during 15 May to 15 June 2007–2009 in north-central South Dakota, collected 6,505 locations, and documented 70 summer home ranges. Mean summer home ranges increased temporally during 2007–2009 (P < 0.001) and corresponded to a 41% loss of CRP grasslands in the area (2.3% loss in land cover and approx. 21% loss in cover habitat in the study area) over the duration of the study. Additionally, mean movement between daily locations increased (P < 0.001) from 2007 to 2009. Analysis of covariance models indicated that change in CRP influenced home-range size, and change in CRP and wheat influenced daily movement. Smaller home ranges and reduced movements were associated with greater quantity of CRP available to fawns, and increased movements were associated with more acreage of wheat available to fawns. Fawns shifted resource selection during the summer at a mean age ranging from 48.8 days to 58.6 days, and this shift was associated with height of corn (83–87 cm). During early summer, fawns consistently selected for CRP; selection of wheat progressed temporally from avoidance in 2007 to selection in 2009. During late summer, fawns consistently selected for corn habitat and used CRP at least in proportion to its availability. Reduction in CRP-grasslands seemed to increase fawn home-range size and daily movements and, influenced change in resource selection to wheat. Current legislation mandates continued decrease in CRP enrollment and concomitant increase in the planting of corn for ethanol production. Management of habitat throughout the grasslands of the Northern Great Plains that maximizes cover habitats would provide neonates with adequate cover for protection from predators. © 2011 The Wildlife Society.