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1.
    
ABSTRACT Approximately 26% of annual mortality for the endangered Florida Key deer (Odocoileus virginianus clavium) occurs as deer-vehicle collisions (DVCs) on the 5.6-km section of United States Highway 1 (US 1) on Big Pine Key (BPK), but extensive urban development adjacent to sections of US 1 complicates efforts to reduce DVCs. Our objective was to evaluate the effectiveness of the US 1 Project (continuous 2.6-km system of 2.4-m fencing, 2 underpasses, and 4 experimental deer guards constructed on US 1 on BPK) in reducing DVCs along US 1. Deer used the underpasses all 3 postproject years (2003–2005); however, we observed higher underpass use in 2004 and 2005 compared to 2003. Exclusion fencing reduced deer intrusions onto the fenced section of US 1 during the 3-year period (2003, n = 7 deer; 2004, n = 4; 2005, n = 12). With a reduction of deer intrusions onto this section of US 1, DVCs decreased in the fenced area by 73–100%; however, US 1 DVCs within the unfenced sections of US 1 also increased (40%) as expected. In controlling for effects of increasing deer density and traffic volume, study results suggest that highway improvements have decreased the net risk of DVCs along US 1, which indicates that use of deer fencing, deer guards, and underpasses is applicable in other urban communities experiencing unacceptable levels of DVCs.  相似文献   

2.
    
ABSTRACT Status assessment of endangered Florida Key deer (Odocoileus virginianus clavium) is currently limited by a paucity of information regarding population estimates for outer islands, which collectively comprise approximately 70% of potential habitat within the Key deer range. Practical limitations and financial considerations render traditional survey techniques impractical for application on remote outer islands. Our objective was to evaluate the utility of infrared-triggered cameras to estimate Key deer abundance on outer islands. We used digital infrared-triggered cameras and mark-resight methods to estimate Key deer abundance on 20 outer islands. Abundance estimates for primary subpopulations ranged from 15 to 16 for Howe Key, 5 to 10 for Knockemdown complex, and 13 to 17 for Little Pine Key. Other island complexes such as Ramrod Key, Water Key, and Annette complex maintain only small subpopulations (i.e., ≤5 individuals) and other previously inhabited island complexes (e.g., Johnson complex and Summerland Key) no longer maintain subpopulations. Key deer abundance was well below estimated carrying capacities on all outer islands, with larger natural populations occurring closest to Big Pine Key. Our results suggest that camera-based surveys offer a practical method to monitor abundance and population trends of Key deer on outer islands. Our study is the first to estimate Key deer abundance in these areas using technically structured model-based methods and provides managers with current and baseline information regarding Key deer subpopulations.  相似文献   

3.
    
Abstract: Dispersal distances and their distribution pattern are important to understanding such phenomena as disease spread and gene flow, but oftentimes dispersal characteristics are modeled as a fixed trait for a given species. We found that dispersal distributions differ for spring and autumn dispersals of yearling male white-tailed deer (Odocoileus virginianus) but that combined data can be adequately modeled based on a log-normal distribution. We modeled distribution of dispersal distances from 3 distinct populations in Pennsylvania and Maryland, USA, based on the relationship between percent forest cover and mean dispersal distance and the relationship between mean and variance of dispersal distances. Our results suggest distributions of distances for dispersing yearling male white-tailed deer can be modeled by simply measuring a readily obtained landscape metric, percent forest cover, which could be used to create generalized spatially explicit disease or gene flow models.  相似文献   

4.
    
Abstract: The scale at which populations use the landscape influences ecological processes and management decisions. Dispersal and home-range size define the scale of landscape use for many large-mammal species. We measured dispersal and home-range size of yearling male white-tailed deer (Odocoileus virginianus) in southern Texas, and compared our results to values from the literature to understand the implications of dispersal in management of deer populations. We used radiotelemetry to monitor 22 yearling deer on 1 study site from October 1998 to October 1999, and 27 yearling deer on a second study site from October 1999 to October 2000. On the 2 study sites, 68% and 44% of yearling deer established new areas of use 4.4 ± 1.0 km and 8.2 ± 4.3 km, respectively, from the center of their autumn home range. Yearling males with spike antlers (2 points) were less likely to disperse than yearlings with fork antlers (>2 points) on 1 study site. Computer simulation showed that the scale at which deer use the landscape is large compared to property sizes in southern Texas and probably in other areas of the white-tailed deer's range. Differences in scale between land ownership patterns and landscape use by deer may result in a failure to meet management objectives and conflict among managers. High harvest rates for male deer occur in part because deer movements are large relative to property size, creating a “tragedy of the commons.” Cooperative management groups are beneficial if all landowners in an area agree on management objectives. Otherwise, deer-proof fences often are erected to reduce conflicts among property owners.  相似文献   

5.
    
Abstract: The scale at which populations use landscapes influences ecological processes and management. We used dispersal and home-range data of 3 age groups of male white-tailed deer (Odocoileus virginianus) to determine the scale at which management will be effective. Home-range size at 5.5 years of age (182 ha ± 24.9 SE) was 56% smaller (P < 0.001) than home-range size of the same 13 males as yearlings (416 ± 59.4 ha). Percent overlap of yearling and 5.5-year-old home ranges was 62.7 6 10.3% (n = 13). Distance between home-range centers of yearling and mature deer was 1,264.9 ± 407.4 m, including 3 deer that dispersed after 2.5 years of age. Average 95% fixed-kernel home-range size was 207.4 ± 20.4 ha and 225.7 ± 30.1 ha for all mature males in years 1 and 2 of our study, respectively. We found that properties >10,000 ha were needed to manage >50% of original yearling males found on the property, whereas properties of 4,500 ha would maintain 50% of original middle-aged (2.5-4.5 yr of age) and mature males (≥4.5 yr of age). Movements after dispersal were minimal, with deer shifting their center of activity <600 m and <350 m each year for middle-aged and mature males, respectively. These data could be used by managers developing management plans, recommending harvest rates, and interpreting harvest data of male white-tailed deer and by biologists attempting to understand ecological processes such as spread of disease.  相似文献   

6.
    
Restoring male age structure in white-tailed deer populations has become an important objective for many state agencies aimed at improving herd dynamics. Limiting mortality in the yearling (1–2 yr old) age class is a primary consideration, and regional differences in climate, habitat characteristics, hunting regulations, and hunter behavior complicate the understanding of how specific factors influence the risk of mortality. We used Cox proportional hazard modeling to determine the effects of body size, mean distance to road, dispersal behaviors, use of forested land, and use of land open to public hunting on the risk of mortality for a population of radio-collared, yearling males (n = 76) in Sussex County, Delaware, USA. Annual survival averaged 0.55 (95% CI = 0.45–0.68), with harvest accounting for 79% (26/33) of all mortalities. Measurements of body size (chest girth, shoulder height, and total length; cm) influenced dispersal probability but not dispersal distance. The best approximating model for mortality risk included a covariate for landownership, whereby mortality risk increased on public land. Among males who dispersed, longer-distance dispersal was associated with reduced mortality, which contradicts previous research describing dispersal as a high-risk behavior. The effect of landownership on mortality risk has not been previously identified, especially when regulations regarding harvest of yearling males are similar between landownership types. We observed annual survival rates of 0.69 (95% CI = 0.57–0.82) for deer apparently using private land exclusively during the hunting season, and 0.20 (95% CI = 0.11–0.48) for deer that used public land during the hunting season. Survival rates on private land were comparable to those of other regions actively managing male age structure. These results suggest survival of yearling males in the region is influenced by hunter harvest and the risks associated with dispersal may be minimal in areas where harvest pressure is low, although hunter harvest on public land may limit male age structure on a localized scale. © The Wildlife Society, 2019  相似文献   

7.
    
Abstract: Past studies using penned deer provide conflicting results on the age when reliable predictions about antler growth potential in white-tailed deer (Odocoileus virginianus) can be made. We captured wild whitetail males via aerial net gun on 12 ranches in 5 counties in south Texas, USA, from 1999 to 2007 to determine if a reliable juvenile-to-adult relationship in antler development existed. We individually marked and released captured animals at the trap site after we took antler and body measurements. We recaptured marked animals as possible in subsequent years or until we obtained final measurements after legal harvest. Amount of growth in the first set of antlers in whitetail males was a poor predictor of antler growth at maturity. By 4.5 years of age there were no differences (P > 0.05) in antler measurements regardless of the amount of development of the first set of antlers at 1.5 years. We concluded culling of yearling males based on number of antler points would have little positive effect on overall antler quality in future years.  相似文献   

8.
    
Sharpshooting is a proven management technique to lower white-tailed deer (Odocoileus virginianus) densities in areas where hunting is precluded. A donation program that allows for the consumptive use of these culled deer is often necessary to gain public approval for such a program. We culled 40 deer in Indiana using sharpshooting methods (head and neck shot placement) and radiographed the carcasses to determine if lead fragmentation spread throughout the skeletal muscle system. In 30 deer where shot placement was between the cranium and fourth cervical vertebrae, we observed no lead fragments in any thoracic or crural muscle tissue. Of 10 deer where shot placement was between the fifth and seventh cervical vertebrae, 8 deer experienced lead fragments in the extensor spinae muscle. Deer culled with highly frangible bullets via sharpshooting in the cranium or upper cervical spine have minimal risk of experiencing lead fragmentation in the thoracic or crural muscle systems. Deer shot in the lower neck may experience lead fragmentation in the anterior extensor spinae muscle, and up to 40 cm of that muscle should be removed before consumption. © 2011 The Wildlife Society.  相似文献   

9.
    
ABSTRACT Demarais and Strickland presented several questions about the scope and validity of conclusions regarding predictability of mature antler size based on yearling antler size and produced a simulation model reported to demonstrate measurement bias in our 2008 study. We believe our conclusions were appropriate with our research hypothesis and demonstrated the assumed differential selection bias by hunters used in Demarais and Strickland was unwarranted. Demarais and Strickland provided no metadata to document the provenance of data used in their model and did not account for location, year, cohort, nutrition of research animals, or loss of individuals from their sample population by accidents or death: the same questions raised in their critique. Additionally, selection and experimental design problems in a portion of their sample population indicate their model results are questionable. Our responses to Demarais and Strickland will aid wildlife managers in making future culling decisions in white-tailed deer management.  相似文献   

10.
    
ABSTRACT Debate within the popular and technical literature regarding predictability of antler size at maturity based on 1.5-year antler size in white-tailed deer (Odocoileus virginianus) has led to confusion and uncertainty within constituent groups. Koerth and Kroll (2008) provided measures of age-related antler development using recaptures of known-age males from 12 deer populations in southern Texas. Several design and analysis issues reduce the scope and validity of their conclusion that amount of growth in the first set of antlers was a poor predictor of antler growth at maturity. Although unstated, the statistical hypothesis they tested did not coincide with their specific conclusions. Using a simulation, we show that their methods were susceptible to measurement bias. Their results are applicable only to populations with similar culling and management programs. Additionally, we provide recommendations for future research projects that evaluate predictability of antler size at maturity based on antler size at younger ages.  相似文献   

11.
    
White-tailed deer (Odocoileus virginianus) are a cervid species found mostly in the Americas. Managing white-tailed deer requires understanding their relationship with the environment, which was characterized by Roseberry and Woolf (Wildlife Society Bulletin 1, 1998, 252) for all counties in Illinois, USA, who incorporated habitat quantity and quality in a deer habitat suitability index. However, this index was based on satellite imagery from 1996 and did not explore the smaller spatial scales used by deer. Our study addressed these gaps by developing a deer land cover utility (LCU) score for each TRS (township, range, and section), township, and county in Illinois based on the methodology outlined in Roseberry and Woolf (Wildlife Society Bulletin 1, 1998, 252) but using data from the National Land Cover Database (2001–2021). These deer LCU scores were validated against minimum deer population data using Bayesian regression with additional covariates relevant to hunting and deer density. These models performed well with Bayesian R2 values of 0.501 (TRS), 0.5 (township), and 0.969 (county). The regression coefficients for the deer LCU scores were statistically significant (95% credibility interval not containing 0) and positive at the TRS, township, and county levels, reflecting the expected relationship between minimum deer density and deer LCU. Predictions made by these regression models on new data were accurate, with the median absolute difference between the true and predicted values being 0.398 deer/km2 for TRS', 0.085 deer/km2 for townships, and 0.066 deer/km2 for counties. This deer LCU could be used in other studies about deer in Illinois or studies in which deer are a relevant factor such as investigations about deer disease or tick distribution. This modeling approach could also be adapted to different wild species, locations, and/or time periods for which land cover data is available.  相似文献   

12.
    
Abstract: Natural and anthropogenic landscape features, such as rivers, mountain ranges, and roads can alter animal dispersal paths and movement patterns. Consequently landscape, through its effects on dispersal, may influence many ecological processes, including disease transmission, invasion dynamics, and gene flow. To investigate influences of landscape features on dispersal patterns of a large mammal, we captured and radiomarked 363 juvenile male white-tailed deer (Odocoileus virginianus), including 212 confirmed dispersers, in 2 topographically dissimilar study areas in Pennsylvania, USA. Dispersal azimuths were uniformly distributed in the western study area (WSA), where there was irregular, hilly topography. Mean dispersal azimuths paralleled ridge direction in the eastern study area, where long parallel ridges were aligned northeast-southwest. Major roads in both areas and a large river in the WSA were semipermeable barriers to dispersal of juvenile males; dispersal paths were less likely to intersect these linear features. Dispersal movements were direct and brief, typically lasting <12 hours. For all dispersers, we found no evidence for preference or avoidance of establishing adult, postdispersal ranges in proximity to roads; however, deer that encountered roads near the terminus of their dispersal path were more likely to stop on the near side. Further, for deer that established postdispersal home ranges near major roads, these features influenced range placement such that locations were typically clustered on one side of the road. The influence of roads, rivers, and mountains on dispersal paths and postdispersal locations of white-tailed deer suggest that landscape-specific features should be considered in conservation and management of this and possibly other species of large mammals.  相似文献   

13.
    
ABSTRACT The sex-age-kill (SAK) model is widely used to estimate abundance of harvested large mammals, including white-tailed deer (Odocoileus virginianus). Despite a long history of use, few formal evaluations of SAK performance exist. We investigated how violations of the stable age distribution and stationary population assumption, changes to male or female harvest, stochastic effects (i.e., random fluctuations in recruitment and survival), and sampling efforts influenced SAK estimation. When the simulated population had a stable age distribution and λ > 1, the SAK model underestimated abundance. Conversely, when λ < 1, the SAK overestimated abundance. When changes to male harvest were introduced, SAK estimates were opposite the true population trend. In contrast, SAK estimates were robust to changes in female harvest rates. Stochastic effects caused SAK estimates to fluctuate about their equilibrium abundance, but the effect dampened as the size of the surveyed population increased. When we considered both stochastic effects and sampling error at a deer management unit scale the resultant abundance estimates were within ±121.9% of the true population level 95% of the time. These combined results demonstrate extreme sensitivity to model violations and scale of analysis. Without changes to model formulation, the SAK model will be biased when λ ≠ 1. Furthermore, any factor that alters the male harvest rate, such as changes to regulations or changes in hunter attitudes, will bias population estimates. Sex-age-kill estimates may be precise at large spatial scales, such as the state level, but less so at the individual management unit level. Alternative models, such as statistical age-at-harvest models, which require similar data types, might allow for more robust, broad-scale demographic assessments.  相似文献   

14.
    
Radiotelemetry and unmarked occupancy modeling have been used to estimate animal population growth, but have not been compared for ungulates. We compared white-tailed deer (Odocoileus virginianus) population growth estimates from radiomarked individuals and occupancy modeling of unmarked individuals and evaluated advantages and disadvantages of each method. Estimates of population growth were obtained using remote camera (N = 54/year) detection/non-detection occupancy surveys of unmarked deer and from survival and recruitment data of radiomarked adult females (N = 87) and neonate fawns (N = 127) in a predominantly forested region of the Upper Peninsula of Michigan, USA, 2009–2011. We hypothesized that occupancy models and radiotelemetry data would have similar population growth trends because both methods sampled the same temporally closed population. Percent changes in camera trap data generally reflected finite population growth (λ) of radiomarked deer which increased (λ = 1.10 ± 0.01) from 2009 to 2010, but decreased (λ = 0.87 ± 0.02) from 2010 to 2011. Also, unmarked adult female abundance and fawn:adult female ratios generally reflected trends in radiomarked deer survival and recruitment. Royle–Nichols occupancy model abundance estimates had wide confidence intervals, which may preclude using this method from accurately estimating deer population growth. Radiotelemetry provided more precise population growth estimates, while allowing collection of vital rates and location data. However, the Royle–Nichols occupancy model may be preferred to radiotelemetry because it reflected yearly variation in population growth with reduced labor and no invasive marking. Researchers should consider the objectives and logistics of their study when choosing a specific method.  相似文献   

15.
ABSTRACT Behavioral studies of white-tailed deer (Odocoileus virginianus) often assign mother-offspring relationships based on common capture of juveniles with adult deer, assuming that fawns associate closely with mothers. We tested this assumption using genetic parentage to assess mother-offspring relationships within capture groups based on data from 10 polymorphic microsatellite loci. At the 80% confidence level, we assigned maternity to 43% and 51% of juveniles captured with an adult female in 2 respective study areas. Capture with their mother did not differ by sex of juveniles in either study area, and limiting our analysis to capture groups that most represent family groups (i.e., one ad F with 1–3 juv) did not increase maternity assignment (35%). Our results indicate that common capture may be a poor indicator of mother-offspring relationships in many field settings. We recommend genetic verification of family relationships.  相似文献   

16.
    
The performance of 2 popular methods that use age-at-harvest data to estimate abundance of white-tailed deer is contingent on assumptions about variation in estimates of subadult (1.5 yr old) and adult (≥2.5 yr old) male harvest rates. Auxiliary data (e.g., estimates of survival or harvest rates from radiocollared animals) can be used to relax some assumptions, but unless these population parameters exhibit limited temporal or spatial variation, these auxiliary data may not improve accuracy. Unfortunately maintaining sufficient sample sizes of radiocollared deer for parameter estimation in every wildlife management unit (WMU) is not feasible for most state agencies. We monitored the fates of 397 subadult and 225 adult male white-tailed deer across 4 WMUs from 2002 to 2008 using radio telemetry. We investigated spatial and temporal variation in harvest rates and investigated covariates related to the patterns observed. We found that most variation in harvest rates was explained spatially and that adult harvest rates (0.36–0.69) were more variable among study areas than subadult harvest rates (0.26–0.42). We found that hunter effort during the archery and firearms season best explained variation in harvest rates of adult males among WMUs, whereas hunter effort during only the firearms season best explained harvest rates for subadult males. From a population estimation perspective, it is advantageous that most variation was spatial and explained by a readily obtained covariate (hunter effort). However, harvest rates may vary if hunting regulations or hunter behavior change, requiring additional field studies to obtain accurate estimates of harvest rates. © 2011 The Wildlife Society.  相似文献   

17.
    
ABSTRACT Understanding sources of male deer mortality is a prerequisite to a successful management program, especially in Texas, USA, where white-tailed deer (Odocoileus virginianus) are the most economically important game species. South Texas, USA, is one of the few areas where males reach older age classes (> 4.5 yr), in part because of intense population management. Therefore, we obtained survival rates and causes of mortality of 48 mature male deer in south Texas, USA, over 2 years. We calculated Kaplan—Meier survival estimates during 2 study years modified for a staggered-entry design and annual survival rates for one cohort of deer from 1998 to 2004 using recapture and radiotelemetry data. We documented 21 mortalities (16 harvest and 5 nonhunting mortalities). Average annual survival of the known-aged 1998 cohort was 82% with 52% of surviving to 6.5 years of age. Survival in study year 2 (0.497 ± 0.069) was less than in study year 1 (0.781 ± 0.073; P = 0.0047), largely because males had finally reached harvestable age (> 6.5 yr old). All but one non-harvest mortality occurred during the rut or postrut periods. It appears that a large percentage of males can reach mature age classes under intense population management, making them available for harvest when at peak antler size. This allows for increased economic returns on intensively managed white-tailed deer populations.  相似文献   

18.
    
ABSTRACT In North America and Europe, deer (Cervidae)—vehicle collisions (DVCs) are common and result not only in injury and death to the animals involved, but also human injury and property damage. Given that most DVCs occur during crepuscular periods, we questioned whether the perceived threat to deer posed by vehicle approach could be enhanced. We hypothesized that a vehicle-based lighting system that better complements peak visual capabilities of deer at night relative to standard tungsten-halogen (TH) lighting alone would elicit a greater flight-initiation distance (FID) by free-ranging white-tailed deer (Odocoileus virginianus). Our lighting system comprised 2 TH lamps and one Xenarc high-intensity discharge (HID) lamp. We defined an a priori logistic model comprising 4 variables potentially explaining deer FID relative to vehicle approach: 1) starting distance of the approach, 2) lighting treatment, 3) season, and 4) deer group size. Deer exposed to the combination of TH lamps and constant illumination of the HID lamp exhibited a mean (SD) FID of 136 (127) m. In contrast, deer exposed to TH lamps only initiated flight on average at 116 (127) m, and those exposed to the combination of TH lamps and the HID lamp pulsed at 2 Hz exhibited a mean FID of 89 (98) m. We contend that the pulsing of the HID lamp while TH lamps were illuminated resulted in consistent loss (over approx. 0.5-sec intervals) of a portion of the image on approach, possibly interfering with sensory information relative to the position of the potential threat. In contrast, the combination of TH lamps and constant illumination of the HID lamp contributed (P = 0.033) to the probability of a FID ≥94 m. We suggest, therefore, that deer FID can be increased by combining currently available TH and HID lamps, or use of HID lamps alone, to enhance detection of an approaching vehicle at night. Also, we encourage research into new lamp designs to better complement deer visual capabilities as well as continued research to quantify deer FID in response to vehicle approach at night and lamp-specific properties that can enhance deer detection of the vehicle.  相似文献   

19.
    
Movements of male white-tailed deer (Odocoileus virginianus) are of great concern with respect to spread of chronic wasting disease (CWD) across landscapes because most yearlings males disperse and adult males have higher prevalence of CWD than do females and younger deer. We radiocollared and monitored 85 male white-tailed deer in the middle Missouri River Valley of eastern Nebraska and western Iowa, USA from 2004 to 2008. Average size (±SE) of fixed-kernel annual home ranges (95%) and core areas (50%) for resident deer were 449 (±32) ha and 99 (±7) ha, respectively. Resident deer exhibited a high-degree of fidelity to their home ranges. Mean overlap between consecutive annual home ranges and core areas was 81% and 74%, respectively. Average dispersal distance was 17.7 ± 4.5 km (range = 3–121 km) for 22 radio-marked and 6 ear-tagged yearlings. Mean spring dispersal distance (25 km) was 150% greater than fall (10 km). Dispersal direction from Desoto National Wildlife Refuge (DNWR) was bimodal on a northwest to southeast axis that followed the Missouri River corridor. Of 22 yearlings that dispersed, 18 (82%) established adult home ranges within the river valley. Dispersal movements of yearling males represent the greatest risk for rapid spread of diseases from infected source populations. Disease management efforts in riparian habitats should target male fawns and yearling males for removal in areas within or immediately adjacent to river corridors. © 2011 The Wildlife Society.  相似文献   

20.
    
Mitochondrial DNA (mtDNA) was used to characterize patterns of geographic variation among white-tailed deer (Odocoileus virginianus) populations in the southeastern United States. Fifteen restriction enzymes were employed to survey and map 99 restriction sites in 142 deer from 18 localities in five southeastern states. Phylogenetic analysis revealed three primary groups of haplotypes: (1) southern Florida and the Florida Keys, (2) the remainder of peninsular Florida northward to South Carolina, and (3) the Florida panhandle westward to Mississippi. Geographical heterogeneity in haplotype frequencies suggests that stochastic lineage sorting or isolation by distance are not important determinates of mtDNA differentiation among deer populations. The pattern of mtDNA variation in white-tailed deer is concordant spatially with those observed in unrelated taxa suggesting the common influence of historical biogeographic events. The data (1) support previous hypotheses that relate contemporary patterns of intraspecific phylogeography in northern Florida to the physiogeographic history of the region; and (2) suggest that genetic differentiation in southern Florida may be attributable to episodes of Pleistocene dispersal. Despite potentially high vagility and human intervention, ecological and demographic characteristics of deer have effectively preserved the historical pattern of intraspecific mtDNA differentiation.  相似文献   

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