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Chronic by-catch of diamondback terrapins (Malaclemys terrapin) in blue crab (Callinectes sapidus) pots is a concern for terrapin conservation along the United States Atlantic and Gulf of Mexico coasts. Despite the availability of by-catch reduction devices (BRDs) for crab pots, adoption of BRDs has not been mandated and by-catch of terrapins continues. We conducted experimental fishing studies in North Carolina's year-round blue crab fishery from 2000 to 2004 to evaluate the ability of various BRDs to reduce terrapin by-catch without a concomitant reduction in the catch of blue crabs. In 4,822 crab pot days fished, we recorded only 21 terrapin captures. Estimated capture rates were 0.003 terrapins/pot per day in hard crab experimental fishing and 0.008 terrapins/pot per day in peeler experimental fishing. All terrapin captures occurred from April to mid-May within 321.4 m of the shoreline. Longer soak times produced more dead terrapins, with 4 live and 4 dead during hard crab experimental fishing and 11 live and 2 dead during peeler experimental fishing. The 4.0-cm BRDs in fall and 4.5-cm and 5.0-cm BRDs in spring reduced the catch of legal-sized male hard crabs by 26.6%, 21.2%, and 5.7%, respectively. Only the 5.0-cm BRDs did not significantly affect the catch of legal-sized hard male crabs. However, BRDs had no measurable effect on catch of target crabs in the peeler crab fishery. Our results identify 3 complementary and economically feasible tools for blue crab fishery managers to exclude terrapins from commercially fished crab pots in North Carolina: 1) gear modifications (e.g., BRDs); 2) distance-to-shore restrictions; and 3) time-of-year regulations. These measures combined could provide a reduction in terrapin by-catch of up to 95% without a significant reduction in target crab catch.
We conducted extensive behavioral and food sampling of Atlantic brant (Branta bernicla hrota) across their winter range and used time-activity budgets for brant to determine daily energy expenditure (DEE). Sampling occurred 1 December—31 May 2006–2008 in 11,225-km2 sites between Rhode Island and Virginia containing important estuarine and upland habitat. To calculate DEE we used instantaneous scan sampling to estimate time-activity budgets. We also determined foods eaten by brant and energy density of food plants. Last, we quantified body condition of brant, which differed among years, months, regions, and ages, and sexes. Overall DEE for brant was 1,530 ± 64 kJ/day. There was considerable variation in time— activity budgets among years, months, regions, habitat, tide, temperature, and time-of-day, but we detected no significant difference in DEE of brant between years or among regions. However, DEE in January (2,018 ± 173 kJ/day) was nearly double the DEE of brant in May (1,048 ± 137 kJ/day). Brant spent their time feeding (32.3%), swimming (26.2%), resting (16.2%), and flying (14.5%). The percent of brant foreguts sampled contained macroalgae (53%) eelgrass (Zostera marina; 18%), salt marsh cordgrass (Spartina alterniflora; 17%), and terrestrial grass (Poa. sp.) and clover (Trifollium sp.; 9%). Energy density differed by vegetation type: macroalgae (12.6 ± 0.1 kJ/g), eelgrass (14.1 ± 0.1 kJ/g), new-growth salt marsh cordgrass (16.9 ± 0.2 kJ/g), and terrestrial grass and clover (17.7 ± 0.1 kJ/g). Atlantic brant exhibited behavioral plasticity thereby allowing modification of daily activity budgets to meet seasonally varying energetic requirements associated with wintering and spring staging. Recognizing a variable DEE can be used along with eventual estimates of food biomass and total metabolizable energy on the landscape to calculate carrying capacity (goose use days) on state, region, or range-wide scales.
Researchers often consider the importance of minimizing holding time during research activities; however, the long-term costs of such handling stress is rarely measured explicitly. As part of an ongoing study of common eiders (Somateria mollissima) at a breeding colony in East Bay, Southampton Island, Nunavut, we recorded duration of restraint for females captured during avian cholera epizootics (2007 and 2008) and monitored female fates (breeding probability, onset of laying, and survival) relative to holding time. Probability of death increased with holding time in 2007 from an estimated 0.05 for females held 20 min to 0.33 for females held for 150 min. In 2008, we responded by limiting holding time to <90 min and mortality was no longer positively correlated with holding time, although total mortality was greater due to increased severity of avian cholera. In both years, longer restraint durations delayed onset of egg-laying after capture by 0.5 days for each 10 min of additional restraint but did not prevent breeding. This delay of nest initiation did not enhance survival probability. Our results show that prolonged holding time can exacerbate mortality during epizootics and emphasize the importance of minimizing restraint time in wild birds, especially in the presence of diseases.
The common loon (Gavia immer) breeds during the summer on northern lakes and water bodies that are also often desirable areas for aquatic recreation and human habitation. In northern New England, we assessed how the spatial nature of disturbance affects common loon nest site selection and territory success. We found through classification and regression analysis that distance to and density of disturbance factors can be used to classify observed nest site locations versus random points, suggesting that these factors affect loon nest site selection (model 1: Correct classification = 75%, null = 50%, K = 0.507, P < 0.001; model 2: Correct classification = 78%, null = 50%, K = 0.551, P < 0.001). However, in an exploratory analysis, we were unable to show a relation between spatial disturbance variables and breeding success (P = 0.595, R2 = 0.436), possibly because breeding success was so low during the breeding seasons of 2007–2008. We suggest that by selecting nest site locations that avoid disturbance factors, loons thereby limit the effect that disturbance will have on their breeding success. Still, disturbance may force loons to use sub-optimal nesting habitat, limiting the available number of territories, and overall productivity. We advise that management efforts focus on limiting disturbance factors to allow breeding pairs access to the best nesting territories, relieving disturbance pressures that may force sub-optimal nest placement.
Much of the breeding range for the mountain plover (Charadrius montanus) occurs in shortgrass steppe and mixed-grass prairie in the western Great Plains of North America. Studies of mountain plovers in shortgrass steppe during the 1970s and 1990s were focused in Weld County, Colorado, which was considered a key breeding area for the species. These studies, however, did not include habitats influenced by black-tailed prairie dogs (Cynomys ludovicianus) or prescribed fire. The role of these 2 rangeland disturbance processes has increased substantially over the past 15 years. During 2008–2009, I used radial distance point count surveys to estimate mountain plover densities early in the nesting season in 4 habitats on public lands in Weld County, Colorado. All 4 habitats were grazed by cattle during the growing season at moderate stocking rates but had different additional disturbances consisting of 1) dormant-season prescribed burns, 2) active black-tailed prairie dog colonies, 3) black-tailed prairie dog colonies affected by epizootic plague in the past 1–2 years, and 4) rangeland with no recent history of fire or prairie dogs. Mountain plover densities were similar on active black-tailed prairie dog colonies ( = 6.8 birds/km2, 95% CI = 4.3–10.6) and prescribed burns ( = 5.6 birds/km2, 95% CI = 3.5–9.1). In contrast, no plovers were detected at randomly selected rangeland sites grazed by cattle but lacking recent disturbance by prairie dogs or fire, even though survey effort was highest for this rangeland habitat. Mountain plover densities were intermediate (2.0 birds/km2, 95% CI = 0.8–5.0) on sites where black-tailed prairie dogs had recently been extirpated by plague. These findings suggest that prescribed burns and active black-tailed prairie dog colonies may enhance breeding habitat for mountain plovers in shortgrass steppe and illustrate the potential for suppressed or altered disturbance processes to influence habitat availability for declining wildlife species.
Loss of breeding habitat and nest predation have contributed to the decline of many shorebird species. The United States Army Corps of Engineers (USACE) initiated a piping plover (Charadrius melodus) habitat creation and augmentation program on the Missouri River in the summer of 2004. The USACE increased unvegetated sandbar habitat by depositing dredged material (engineered sandbars) and by clearing vegetation from existing sandbars (managed sandbars). We evaluated the effects of this increase in nesting and foraging habitat on habitat selection and nest daily survival rate (DSR) of piping plovers on Lewis and Clark Lake and the Gavins Point Reach of the Missouri River from 2005 to 2007 (n = 623 nests). Piping plovers selected engineered sandbars more often than expected based on area and selected natural and managed habitats less than expected based on area. Daily survival rate on engineered sandbars was significantly higher than on natural or managed sandbars (log odds: 2.50, 95% CI: 1.05–5.94). Thus, plovers' habitat selection may have increased their nesting success. Our results suggest that habitat augmentation may stave off declines in piping plover populations limited by insufficient habitat and low nesting success.
To assess and improve existing monitoring protocols for sharp-tailed grouse (Tympanuchus phasianellus) in the eastern Upper Peninsula of Michigan, we used data from 58 radio-collared grouse (46 M, 12 F) monitored within 3 openland landscape types: a xeric, conifer-dominated site, a wetland-dominated site, and a site dominated by low-intensity agriculture. We used lek counts and radio telemetry to determine lek attendance rates, factors affecting lek attendance rates, lek fidelity, and inter-sexual variation in these parameters. Our analysis indicated lek attendance varied with respect to sex of bird, day of year, time after sunrise, and wind speed. Peak male lek attendance rates exceeded those of females by up to 40%, and peak lekking activity for both males and females occurred during the second and third weeks of April. Male lekking activity occurred earlier and was sustained longer than that of females. Lekking activity was negatively related to time of day and wind speed. We observed strong lek fidelity as radio-collared birds attended a primary lek 94% of the time, indicating a low probability of multiple counting of individual birds. We also proposed a method to adjust lek count data for the probability that birds are on a lek during lek counts. Our proposed method can be used by researchers and managers to improve estimates of the number of birds attending a lek by reducing the negative bias associated with observed counts.
Models are important tools that can help managers and researchers understand the population dynamics of a species and how different habitat or population management scenarios impact that species. We used radio-telemetry data from northern bobwhites (Colinus virginianus) in southern Texas from 2000 to 2005 to develop a stochastic simulation model for bobwhite populations. Our model is based on difference equations, with stochastic variables drawn from normal and Weibull distributions. We simulated bobwhite populations to 100 yr and evaluated our model by comparing results with independent estimates of 4 population parameters (spring and fall density, finite rate of increase in the fall population [λ], and winter juv:ad age ratios). Using a quasi-extinction criterion of ≤40 birds (density = ≤0.05 birds/ha), probability of persistence to 100 yr was 88.3% (106 of 120 simulations) for the spring population and 96.7% (116 of 120 simulations) for the fall population. Using a less restrictive quasi-extinction criteria (≤ 14 birds), probability of persistence was 93.3% (112 of 120 simulations) for the spring population and 98.3% (118 of 120 simulations) for the fall population. Simulated population parameters were similar to independent estimates for 4 of 4 population parameters. Winter age ratios differed between our model ( = 4.98 juv:ad, n = 120, SE = 0.32) and empirical age ratios from harvested bobwhites on our study area ( = 2.85 juv:ad, n = 25, SE = 0.24). However, when we corrected harvest age ratios for bias in juvenile harvest ( = 3.85 juv:ad, n = 25, SE = 0.32) simulated and empirical estimates were similar. Our model appears to be a reliable predictor of bobwhite populations in the southern Texas. Our simulation results indicate that bobwhite hunters and managers can expect excellent bobwhite hunting (fall populations ≥2.2 birds per ha) in about one of 10 yr.
KEYWORDS: California spotted owls, radio-telemetry, random sampling design, resource selection function, Sierra Nevada, Strix occidentalis occidentalis
We studied home range and habitat selection of radio-marked adult California spotted owls (Strix occidentalis occidentalis) randomly selected from among the breeding population of owls in the central Sierra Nevada, California from June to October 2006. The most parsimonious home-range estimate for our data was 555 ha (SE = 100 ha). Home-range size was positively correlated with the number of vegetation patches in the home range (habitat heterogeneity). We used resource selection ratios to examine selection of vegetation types by owls within our study area. Owl home ranges contained a high proportion of mature conifer forest, relative to its availability, although the confidence interval for this estimate overlapped one. We also used resource selection functions (RSF) to examine owl foraging habitat selection. Relative probability of selection of foraging habitat was correlated with vegetation classes, patch size, and their interaction. Owls showed highest selection rates for large patches (>10 ha) of pole-sized coniferous forest. Our results suggested that spotted owls in the central Sierra Nevada used habitat that contained a high proportion of mature conifer forest at the home-range scale, but at a finer scale (foraging site selection) owls used other vegetation classes interspersed among mature forest patches, consistent with our hypothesis that spotted owls may use other forest types besides old growth and mature forests when foraging. Our study provides an unbiased estimate of habitat use by spotted owls in the central Sierra Nevada. Our results suggest that forest managers continue to protect remaining mature and old-growth forests in the central Sierra Nevada because owl home ranges contain high proportions of these habitats. However, our results also showed that owls used younger stands as foraging habitat so that landscape heterogeneity, with respect to cover types, may be an important consideration for management but we did not attempt to relate our findings to fitness of owls. Thus management for some level of landscape heterogeneity for the benefit of owls should proceed with caution or under an adaptive management framework.
The effects that changes in forest structure and composition have on wildlife have often been considered independently, such that the potential for interactive effects has received relatively little attention. We investigated the importance of vegetation structure, floristic composition, and their interaction for predicting bird distribution in mixed broadleaf—conifer forest. We collected vegetation and bird data at 979 stations in a watershed in southern Oregon in the spring of 2001. At each station, we described the vegetation using measures of structure (total vegetation volume) and of floristic composition (broadleaf-conifer composition). We then used logistic regression to model the probability of occurrence of bird species as a function of these 2 variables, their quadratic terms, and their interaction. Using stepwise model selection we identified the best model for each species and used area under the curve (AUC) scores to evaluate model performance. Of the 44 bird species we investigated, 20 had models with AUC scores ≥0.70. Of the best models for these 20 species, 1 included vegetation composition alone, 12 included just the main effects of vegetation composition and structure, and 7 included both the main effects and interaction terms. In summer of 2001 a wildfire burned 2,500 ha of the study area, resulting in substantial changes in the vegetation structure and composition. We used 4 yr of postfire bird and vegetation surveys to test the predictive performance of the habitat models for 9 species that occurred at >15% of the burned stations. Models for 3 of these species performed poorly (AUC < 0.7) in all 4 yr. For the other 6 species, predictive performance was low in the first year after fire and improved during subsequent years, suggesting a lagged response to changes in vegetation structure and composition. Quantifying the interactive effects of vegetation structure and composition improves our understanding of how birds respond to forest management and large-scale disturbances, such as wildfires.
We determined efficacy of AV-1011® (a 50% anthraquinone product; Arkion® Life Sciences, New Castle, Delaware) on drill-planted rice seed to reduce blackbird damage and determine residue levels of anthraquinone (AQ) in rice seeds and seedlings and in the mature rice crop under field enclosures at the University of Missouri-Delta Center farm near Portageville, Missouri. Red-winged blackbird (Agelaius phoeniceus) damage was higher for untreated than AV-1011® treated rice seedlings at assessment period 3, 15 days postplanting (F1,141 = 15.81, P < 0.001), and at assessment period 4, 19 days postplanting F1,136 = 11.54, P = 0.001). Blackbird damage to AV-1011-treated seedling for assessment periods 3 and 4 was 8% and 7%, respectively, while blackbird damage to untreated seedlings during the same assessment periods was 52% and 44%. More blackbirds used untreated plots than AV-1011-treated plots during assessment periods 2–4 (F1,17.8 = 20.02, P < 0.001). Overall concentrations of AQ on seeds averaged 5,993 µg/g or 0.59% during the test period. Concentrations of AQ in mature rice seed and plant collected at harvest averaged 1.22 µg/g and 0.10 µg/g, respectively. AV-1011 offers promise for reducing bird depredations to newly planted rice, but additional testing should be conducted to evaluate this repellent in a large-scale field setting.
Sylvatic plague (Yersinia pestis) is an exotic pathogen that is highly virulent in black-tailed prairie dogs (Cynomys ludovicianus) and causes widespread colony losses and individual mortality rates >95%. We investigated colony spatial characteristics that may influence inter-colony transmission of plague at 3 prairie dog colony complexes in the Great Plains. The 4 spatial characteristics we considered include: colony size, Euclidean distance to nearest neighboring colony, colony proximity index, and distance to nearest drainage (dispersal) corridor. We used multi-state mark—recapture models to determine the relationship between these colony characteristics and probability of plague transmission among prairie dog colonies. Annual mapping of colonies and mark—recapture analyses of disease dynamics in natural colonies led to 4 main results: 1) plague outbreaks exhibited high spatial and temporal variation, 2) the site of initiation of epizootic plague may have substantially influenced the subsequent inter-colony spread of plague, 3) the longterm effect of plague on individual colonies differed among sites because of how individuals and colonies were distributed, and 4) colony spatial characteristics were related to the probability of infection at all sites although the relative importance and direction of relationships varied among sites. Our findings suggest that conventional prairie dog conservation management strategies, including promoting large, highly connected colonies, may need to be altered in the presence of plague.
In the early 1990s the Nelchina Caribou (Rangifer tarandus) Herd (NCH) began a dramatic shift to its current winter range, migrating at least an additional 100 km beyond its historic range. We evaluated the impacts of fire and grazing history on lichen abundance and subsequent use and distribution by the NCH. Historic (prior to 1990) and current (2002) winter ranges of the NCH had similar vascular vegetation, lichen cover (P = 0.491), and fire histories (P = 0.535), but the former range had significantly less forage lichen biomass as a result of grazing by caribou. Biomass of forage lichens was twice as great overall (P = 0.031) and 4 times greater in caribou selected sites on the current range than in the historic range, greatly increasing availability to caribou. Caribou on the current range selected for stands with >20% lichen cover (P < 0.001), greater than 1,250 kg/ha (P < 0.001) forage lichen biomass and stands older than 80 yr postfire (P < 0.001). After fires, forage lichen cover and biomass seldom recovered sufficiently to attract caribou grazing until after ≥60 yr, and, as a group, primary forage lichen species did not reach maximum abundance until 180 yr postfire. Recovery following overgrazing can occur much more quickly because lichen cover, albeit mostly fragments, and organic substrates remain present. Our results provide benchmarks for wildlife managers assessing condition of caribou winter range and predicting effects of fires on lichen abundance and caribou distribution. Of our measurements of cover and biomass by species, densities and heights of trees, elevation, slope and aspect, only percentage cover by Cladonia amaurocraea, Cladina rangiferina, Flavocetraria cuculata, and lowbush cranberry (Vaccinium vitis-idaea) were necessary for predicting caribou use of winter range.
Understanding the social dynamics of large carnivores is critical to effective conservation and management planning. We made the first attempt to delineate both paternity and relatedness for a population of cougar (Puma concolor) using microsatellite data. We analyzed a long-term genetic dataset collected from a hunted population in the Garnet Mountains of western Montana. We assigned paternity for 62.5% of litters sampled using both exclusion and likelihood analyses. Attempts at reconstructing unsampled paternal genotypes resulted in delineating possible sires for 8 more litters. Sires were on average younger than reported for males involved in pairings assessed via field data in other cougar populations. Although most mating pairs were unrelated, 5 of 17 pairings involved cougars with levels of relatedness corresponding to half-sibling and full-sibling or parent offspring relationship (r = 0.215–0.575). Relatedness among adult and subadult males was higher than relatedness levels among adult and subadult females. Relatedness among males in the Garnet population differed from patterns hypothesized to occur under male-biased dispersal theories for cougars. The long-term impact of the turnover of resident cougars in hunted populations is still unclear and warrants additional research. Our results highlight the utility of monitoring cougar demographic parameters using a combination of genetic and field data that in turn may assist managers with determining cougar harvest quotas or strategies, harvest seasons, sustainable harvest, and the appropriate management level of cougar populations.
The recent introduction of red foxes (Vulpes vulpes) to Australia's island state of Tasmania represents a major threat to native fauna. In response, the Tasmanian government has begun a fox eradication program using Foxoff®, a bait containing the poison sodium monofluoroacetate (commonly known as 1080). The bait is potentially attractive to native Tasmanian carnivores as well as to foxes. Of particular concern is the endangered Tasmanian devil (Sarcophilus harrisii), which is already at risk from an emergent infectious disease, devil facial tumor disease (DFTD). In both a captive and a field study using non-toxic Foxoff bait, we assessed bait palatability and possible effects of demographics, hunger level, bait age, and bait burial method on the likelihood of bait uptake by Tasmanian devils. Captive devils showed varying interest in the bait, but wild devils appeared to find it uniformly palatable. In the captive study, males and younger, captive-born animals were more likely to excavate and remove bait. Subterranean burial at 15 cm was the most effective deterrent to bait excavation; effectiveness decreased at shallower depths and with surface-level bait buried beneath soil mounds. Our findings suggest that the current fox-baiting campaign may negatively impact individual devils. More extensive study is necessary to assess potential risk at the population level.
The effects of widespread sagebrush removal treatments on pygmy rabbits (Brachylagus idahoensis) are not well understood. Due to reliance on sagebrush, pygmy rabbits are among the species for which these treatments may be detrimental. Our objectives were to evaluate the effects of experimental sagebrush treatment on 8 radio-collared pygmy rabbits between and within home range habitat selection using Monte Carlo simulation from null models. Pygmy rabbits were not extirpated from plots containing habitat treatments, and we found no evidence that treatments affected home range placement. The mean treatment distance of observed home range centers did not differ from repeated trials of random points. However, we found evidence of within home range selection against treatments from 2 of 8 rabbits located close to the treatments. The mean treatment distance of all observed locations for these 2 rabbits was greater than expected based on a null model. We also used snow tracking to show that pygmy rabbits entered treatments in 4 out of 21 trials, which was less often than expected by chance (G2 = 8.662, P = 0.003). Conservatively, sagebrush removal treatments should not be conducted on active or recently active pygmy rabbit burrows. Elsewhere near known pygmy rabbit sites, treated patches should be small and connected by untreated corridors to prevent potentially limiting movement of rabbits among the untreated habitat.
Monitoring the response of endangered and protected species to hydrological restoration is a major component of the adaptive management framework of the Comprehensive Everglades Restoration Plan. The endangered Florida manatee (Trichechus manatus latirostris) lives at the marine-freshwater interface in southwest Florida and is likely to be affected by hydrologic restoration. To provide managers with prerestoration information on distribution and abundance for postrestoration comparison, we developed and implemented a new aerial survey design and hierarchical statistical model to estimate and map abundance of manatees as a function of patch-specific habitat characteristics, indicative of manatee requirements for offshore forage (seagrass), inland fresh drinking water, and warm-water winter refuge. We estimated the number of groups of manatees from dual-observer counts and estimated the number of individuals within groups by removal sampling. Our model is unique in that we jointly analyzed group and individual counts using assumptions that allow probabilities of group detection to depend on group size. Ours is the first analysis of manatee aerial surveys to model spatial and temporal abundance of manatees in association with habitat type while accounting for imperfect detection. We conducted the study in the Ten Thousand Islands area of southwestern Florida, USA, which was expected to be affected by the Picayune Strand Restoration Project to restore hydrology altered for a failed real-estate development. We conducted 11 surveys in 2006, spanning the cold, dry season and warm, wet season. To examine short-term and seasonal changes in distribution we flew paired surveys 1–2 days apart within a given month during the year. Manatees were sparsely distributed across the landscape in small groups. Probability of detection of a group increased with group size; the magnitude of the relationship between group size and detection probability varied among surveys. Probability of detection of individual manatees within a group also differed among surveys, ranging from a low of 0.27 on 11 January to a high of 0.73 on 8 August. During winter surveys, abundance was always higher inland at Port of the Islands (POI), a manatee warm-water aggregation site, than in the other habitat types. During warm-season surveys, highest abundances were estimated in offshore habitat where manatees forage on seagrass. Manatees continued to use POI in summer, but in lower numbers than in winter, possibly to drink freshwater. Abundance in other inland systems and inshore bays was low compared to POI in winter and summer, possibly because of low availability of freshwater. During cold weather, maps of patch abundance of paired surveys showed daily changes in manatee distribution associated with rapid changes in air and water temperature as manatees sought warm water with falling temperatures and seagrass areas with increasing temperatures. Within a habitat type, some patches had higher manatee abundance suggesting differences in quality, possibly due to freshwater flow. If hydrological restoration alters the location of quality habitat, postrestoration comparisons using our methods will document how manatees adjust to new resources, providing managers with information on spatial needs for further monitoring or management. Total abundance for the entire area was similar among survey dates. Credible intervals however were large on a few surveys, and may limit our ability to statistically detect trends in total abundance. Additional modeling of abundance with time- and patch-specific covariates of salinity, water temperature, and seagrass abundance will directly link manatee abundance with physical and biological changes due to restoration and should decrease uncertainty of estimates.
Estimates of utilization distributions (UDs) are used in analyses of home-range area, habitat and resource selection, and social interactions. We simulated data from 12 parent UDs, representing 3 series of increasingly intense space-use patterns (clustering of points around a home site, restriction of locations to a network of nodes and corridors, and dominance of a central hole in the UD) and compared the ability of kernel density estimation (KDE) and local convex hull (LCH) construction to reconstruct known UDs from samples of 10, 50, 250, and 1,000 location points. For KDE, we considered 4 bandwidth selectors: the reference bandwidth, least-squares cross-validation (LSCV), direct plug-in (DPI), and solve-the-equation (STE). For the sample sizes and UD patterns tested here, KDE achieved significantly higher volume-of-intersection (VI) scores with known parent UDs than did LCH; KDE also provided less biased home-range area estimates under many conditions. However, LCH minimized the UD volume that occurred outside the true home range boundary (Vout). Among the KDE bandwidth estimators, relative performance depended on the type and intensity of space use patterns, sample size, and the metric used to evaluate performance. Biologists should use KDE for UD and home range estimation within a probabilistic context, unless their objective is to exclude potentially unused areas by defining the area delimited by data.
Many previous comparisons of multiple sampling methods have assumed that detection probabilities for each method are either constant or equal to one. We used 4 sampling methods to estimate detection probabilities for forest-floor dwelling amphibians, reptiles, and small mammals. We investigated associations between seasonality and precipitation on species detection and explored sample design tradeoffs for future studies. Although we captured 25 species, we could reliably detect (detection probability >0.15) only northern short-tailed shrews (Blarina brevicauda) and pygmy and masked shrews (Sorex spp.) using drift fences and red-backed salamanders (Plethodon cinereus) using visual encounter surveys (VES). The use of multiple sampling methods improved detection probabilities for only red-backed salamanders (VES = 0.32, 95% CI: 0.24–0.38, allmethods = 0.38, 95% CI: 0.32–0.44). Parameter estimates indicated detection of both shrew species was positively related to increased precipitation. Detection probabilities for pygmy and masked shrews and red-backed salamanders were positively and negatively associated with date, respectively. Our power analysis revealed that sampling during rain events increased the power of detecting a change in sorid occupancy by ≥40% (α = 0.05). Our results demonstrate the need to incorporate species detectability when comparing the effectiveness of different trapping methodologies. Furthermore, our study highlights the utility of power analyses for exploring study design tradeoffs for research and monitoring programs.
Despite the efforts of many natural resource professionals, wild pig (Sus scrofa) populations are expanding in many areas of the world. Although many creative techniques for controlling pig populations are being explored, trapping has been and still is the most commonly used method of population control for many public and private land managers. We conducted an observational study to examine the efficiency of 2 frequently used trap styles: a small, portable box-style trap and a larger, semi-permanent, corral-style trap. We used game cameras to examine patterns of trap entry by wild pigs around each style of trap, and we conducted a trapping session to compare trapping success between trap styles. Adult female and juvenile wild pigs entered both styles of trap more readily than did adult males, and adult males seemed particularly averse to entering box traps. Less than 10% of adult male visits to box traps resulted in entries, easily the least percentage of any class at any style of trap. Adult females entered corral traps approximately 2.2 times more often per visit than box traps and re-entered corral traps >2 times more frequently. Juveniles entered and reentered both box and corral traps at similar rates. Overall (all-class) entry-per-visit rates at corral traps (0.71) were nearly double that of box traps (0.37). Subsequent trapping data supported these preliminary entry data; the capture rate for corral traps was >4 times that of box traps. Our data suggest that corral traps are temporally and economically superior to box traps with respect to efficiency; that is, corral traps effectively trap more pigs per trap night at a lower cost per pig than do box traps.
We used female ring-necked pheasant (Phasianus colchicus) carcasses as surrogates for greater sage-grouse (Centrocercus urophasianus) to study factors influencing survival and detection bias associated with avian fence collision surveys in southern Idaho, USA, during spring 2009. We randomly placed 50 pheasant carcasses on each of 2 study areas, estimated detection probability during fence-line surveys, and monitored survival and retention of carcasses and their associated sign over a 31-day period. Survival modeling suggested site and habitat features had little impact on carcass survival, and constant survival models were most supported by the data. Model averaged carcass daily survival probability was low on both study areas and ranged from 0.776 to 0.812. Survival of all carcass sign varied strongly by location, and the top sign survival model included a site effect parameter. Model averaged daily survival probability for collision sign on the 2 study sites ranged from 0.863 to 0.988 and varied between sites. Logistic regression modeling indicated detection probability of carcasses during fence-line surveys for avian collision victims was influenced by habitat type and microsite shrub height at the carcass location. Carcasses located in big sagebrush (Artemisia tridentata) habitats were detected at a lower rate (0.36) than carcasses in little (A. arbuscula) and black sagebrush (A. nova) habitats (0.71). Increasing shrub height at the carcass location from the little sagebrush mean of 16.5 cm to the big sagebrush mean of 36.0 cm reduced detection probability by approximately 30%. Avian fence collision surveys in sagebrush-steppe habitats should be conducted at ≤2-week sampling intervals to reduce the impact of survival bias on collision rate estimates. Two-week sampling intervals may be too long in areas with low carcass and sign survival, therefore survival rates should be estimated on all study areas to determine the appropriate sampling interval duration. Researchers should be aware of the effects of local vegetation on detection probabilities, and methods to correct detection probabilities based on collision site attributes should be applied to ensure more accurate collision rate estimates. Additionally, caution should be used when aggregating or comparing uncorrected collision data from areas with differing vegetation, as detection probabilities are likely different between sites.
Transparency in resource management decisions requires a proper accounting of uncertainty at multiple stages of the decision-making process. As information becomes available, periodic review and updating of resource management protocols reduces uncertainty and improves management decisions. One of the most basic steps to mitigating anthropogenic effects on populations is determining if a population of a species occurs in an area that will be affected by human activity. Species are rarely detected with certainty, however, and falsely declaring a species absent can cause improper conservation decisions or even extirpation of populations. We propose a method to design survey protocols for imperfectly detected species that accounts for multiple sources of uncertainty in the detection process, is capable of quantitatively incorporating expert opinion into the decision-making process, allows periodic updates to the protocol, and permits resource managers to weigh the severity of consequences if the species is falsely declared absent. We developed our method using the giant gartersnake (Thamnophis gigas), a threatened species precinctive to the Central Valley of California, as a case study. Survey date was negatively related to the probability of detecting the giant gartersnake, and water temperature was positively related to the probability of detecting the giant gartersnake at a sampled location. Reporting sampling effort, timing and duration of surveys, and water temperatures would allow resource managers to evaluate the probability that the giant gartersnake occurs at sampled sites where it is not detected. This information would also allow periodic updates and quantitative evaluation of changes to the giant gartersnake survey protocol. Because it naturally allows multiple sources of information and is predicated upon the idea of updating information, Bayesian analysis is well-suited to solving the problem of developing efficient sampling protocols for species of conservation concern.
We studied the effect of great-horned owl (Bubo virginianus) removal on piping plover (Charadrius melodus) hatchling survival on Missouri River sandbars (2008–2009). Owl removal increased daily survival of piping plover chicks in 2008 (β = 2.03, 95% CI: 0.04–4.02), but this effect decreased with increasing age of the chick (β = -0.42, 95% CI: -0.81 to -0.03). Results for 2009 were similar in direction but not significant. Survival was higher in 2008 than in 2009, regardless of owl capture, indicating that even if owl capture consistently were effective at increasing survival, overall survival resulting from trapping may vary annually. Owl trapping was a successful means to raise chick survival on the Missouri River in ≥1 year and could be used at other sites experiencing depressed chick survival due to avian predators.
We designed, deployed, and evaluated a sound broadcast system for use in an experiment investigating response of songbirds to conspecific vocalizations in habitat selection; the system was functional, flexible, and allowed for easy assembly, customization, and repair. Broadcast of sound in the field can enable study of animal response to predators, conspecifics, heterospecifics, noise, and other stimuli and is being considered for a variety of management applications. However, no published method is available for building a sound broadcast system from readily available components for use in the field.
I developed a modified leg harness for mounting radiotelemetry transmitters to small birds, which includes a weak link that allows telemetry equipment to be shed. Over 4 years, I mounted 62 transmitters on 49 Tuamotu kingfishers (Todiramphus gambieri) using weak-link harnesses. Kingfishers retained 86% of transmitters for the duration of monitoring periods (23–66 days) whereas 22 of 23 transmitters were shed from birds resighted after 6–15 months. Apparent mortality was no higher for radio-marked birds than for birds without transmitters. The weak-link harness is an improvement to existing transmitter attachment techniques and provides a useful, effective, and ethical means of studying bird movements.
Camera surveys often involve placing bait in front of the camera to capture animals more frequently, which could introduce biases in parameter estimates. From September 2008 to March 2009, we monitored cameras placed at random, along game trails, and at feed stations to determine if camera placement influenced measures of population demographics in a herd of white-tailed deer (Odocoileus virginianus). There was no time period in which cameras placed at feed stations provided sex ratio and recruitment estimates similar to those acquired from randomly placed cameras. Trail-based camera surveys provided population estimates similar to those from random sites and may provide a feasible alternative to using baited camera stations.
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