Prey behavioral responses to predation risk in wolf‐ungulate‐plant systems are of interest to wildlife managers. Using Global Positioning System data collected from telemetry‐collared elk (Cervus elaphus) and wolves (Canis lupus), we evaluated elk behavioral responses to spatial and temporal variation in wolf‐ and human‐predation risk on a winter range in the Greater Yellowstone Area, USA. We found elk changed grouping patterns and increased movement rates as predation risk increased and that these behavioral changes were habitat dependent. Elk behavioral responses to wolf‐ and human‐predation risk were similar; however, responses to human‐predation risk were stronger than responses to wolf‐predation risk. These results suggest that predation risk from wolves or human hunters may result in elk spending more time on private rangelands away from public‐land winter ranges, which may exacerbate problems of landowner tolerance of elk on livestock pastures. However, increased movement and changing grouping patterns on winter ranges may also disperse elk grazing impacts and lessen elk impacts on any one area.
Summary1. The presence of Brucella abortus within free-ranging wildlife populations is an important conservation and management issue because of the risk of brucellosis transmission between wildlife and livestock. Predicting wildlife distributions is necessary to forecast wildlife and livestock spatial overlap and the potential for brucellosis transmission. 2. We used Global Positioning System data collected from telemetry-collared female elk Cervus elaphus to develop resource selection function (RSF) models during the brucellosis transmission risk period (the abortion and calving periods). We validated extrapolation of predictive models at two nearby elk ranges within the Greater Yellowstone Ecosystem. Additionally, we integrated extrapolated RSF maps and domestic livestock distributions to estimate the relative probability of elk and livestock commingling during the brucellosis transmission risk period. 3. The top-ranked model predicted that areas selected by elk had a lower probability of wolf Canis lupus occupancy, were privately owned and south facing, and had steeper slopes, lower road densities and higher Normalized Difference Vegetation Index (NDVI). Elk selected forests and shrublands over grasslands; however, the strength of selection decreased as snowpack increased. Elk selection for privately owned lands may lead to spatial overlap with livestock and increase the risk of elk and livestock intermingling. Furthermore, if both elk and livestock concentrate in areas of higher NDVI, increased spatial overlap may occur in these areas. 4. Predictive accuracy was highest in the study area where the model was developed. When compared to the model development area, predictive accuracy of extrapolated RSF maps was similar or better in one of the elk ranges and lower in the other elk range. 5. Synthesis and applications. Extrapolated RSF and spatial overlap maps can provide a foundation for identifying the highest risk areas of elk and livestock spatial overlap during the brucellosis transmission risk period. However, the predictive accuracy of the models is limited when applied to different areas. Site-specific models of spatial overlap would therefore be needed to provide the most accurate estimates of elk and livestock spatial overlap during the transmission risk period. The degree to which spatial overlap may lead to actual transmission risk needs to be investigated as this is not yet known and could have important implications for managing transmission risk.
Changes in resource selection associated with human predation risk may alter elk distributions and availability for harvest. We used Global Positioning System data collected from telemetered female elk (Cervus elaphus) to evaluate effects of refuges (areas where hunting was prohibited), spatial variation in hunting risk, and landscape attributes on resource selection within an established Greater Yellowstone Area, USA, winter range. We also evaluated elk distributions during and outside of a late‐season hunting period. Refuge areas and landscape attributes such as habitat type and snow water equivalents (SWE) affected resource selection. Elk selection for flat grasslands increased as SWE increased, likely because these areas were windswept, leaving grasses exposed for foraging. Elk distributions differed during hunting and no‐hunting periods. During the hunting period, elk shifted to privately owned refuge areas and the estimated odds of elk occupying refuge areas more than doubled. Risk‐driven changes in resource selection resulted in reduced availability of elk for harvest. Elk selection for areas where hunting is prohibited presents a challenge for resource managers that use hunting as a tool for managing populations and influences grazing patterns on private ranchlands.
Migration evolved as a behavior to enhance fitness through exploiting spatially and temporally variable resources and avoiding predation or other threats. Globally, landscape alterations have resulted in declines to migratory populations across taxa. Given the long time periods over which migrations evolved in native systems, it is unlikely that restored populations embody the same migratory complexity that existed before population reductions or regional extirpation. We used GPS location data collected from 209 female bighorn sheep ( Ovis canadensis ) to characterize population and individual migration patterns along elevation and geographic continuums for 18 populations of bighorn sheep with different management histories (i.e., restored, augmented, and native) across the western United States. Individuals with resident behaviors were present in all management histories. Elevational migrations were the most common population‐level migratory behavior. There were notable differences in the degree of individual variation within a population across the three management histories. Relative to native populations, restored and augmented populations had less variation among individuals with respect to elevation and geographic migration distances. Differences in migratory behavior were most pronounced for geographic distances, where the majority of native populations had a range of variation that was 2–4 times greater than restored or augmented populations. Synthesis and applications . Migrations within native populations include a variety of patterns that translocation efforts have not been able to fully recreate within restored and augmented populations. Theoretical and empirical research has highlighted the benefits of migratory diversity in promoting resilience and population stability. Limited migratory diversity may serve as an additional factor limiting demographic performance and range expansion. We suggest preserving native systems with intact migratory portfolios and a more nuanced approach to restoration and augmentation in which source populations are identified based on a suite of criteria that includes matching migratory patterns of source populations with local landscape attributes.
We administered a suite of treatments to a herd of Rocky Mountain bighorn sheep (Ovis canadensis canadensis) that was experiencing poor lamb recruitment and showing signs of respiratory disease. Despite 3 yr of treatment with various combinations of anthelmentics, antibiotics, vaccines, and hyperimmune serum products, recruitment was not improved.
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