Landscape-Level Assessment of Brood Rearing Habitat for Greater Sage-Grouse in Nevada

Abstract: Loss of quality brood rearing habitat, resulting in reduced chick growth and poor recruitment, is one mechanism associated with decline of greater sage-grouse (Centrocercus urophasianus) populations. Low chick survival rates are typically attributed to poor-quality brood rearing habitat. Models that delineate suitability of sage-grouse nesting or brood rearing habitat at the landscape scale can provide key insights into the relationship between sage-grouse and the environment, allowing managers to identify and prioritize habitats for protection or restoration. We used Southwest Regional Gap landcover types to identify early and late greater sage-grouse brood rearing in east-central Nevada. We conducted an Ecological Niche Factor Analysis to 1) examine the effect these landcover types and other ecogeographical variables have on sage-grouse selection of brood rearing habitat, and 2) generate landscape-scale suitability maps. We also evaluated if incorporating a fitness component (brood survival) in landscape spatial analyses of habitat quality influenced our assessment of habitat suitability. Because 36% of our 6,500-km² study area was identified as early brood rearing habitat, we believe this habitat may not be limiting greater sage-grouse populations in east-central Nevada, USA, at least in wet years. We found strong selection for particular landcover types (e.g., higher elevation, moist sites with riparian shrubs or montane sagebrush) during late brood rearing. Late brood rearing habitat on which broods were successfully reared represented only 2.8% of the study area and had a restricted distribution, suggesting the potential that such habitat could limit sage-grouse populations in east-central Nevada.     

Achieving Better Estimates of Greater Sage-Grouse Chick Survival in Utah

Abstract: Declining sage-grouse (Centrocercus urophasianus) populations may be characterized by poor recruitment largely attributed to low chick survival. However, few published studies have explicitly examined factors that influence chick survival. We used a suture method to radiomark 1-2-day-old sage-grouse chicks (n = 150) in 2005-2006 on Parker Mountain in south-central Utah, USA, and monitored their survival to 42 days. We modeled effects of year, hatch date, chick age, brood-female age, brood-mixing, and arthropod abundance on chick survival. Our best model revealed an average survival estimate of 0.50 days to 42 days, which is the highest level ever documented for this long-lived species. Brood-mixing occurred in 21% (31/146) of chicks and 43% (18/42) of broods we studied. Moreover, yearling females had more chicks leave their broods than did adults. We found that survival may be higher among chicks that switch broods compared to those that stayed with their natal mother until fledging. Thus, brood-mixing may be an adaptive strategy leading to increased sage-grouse chick survival and higher productivity, especially among chicks born to yearling females. Our findings also indicate that arthropod abundance may be an important driver of chick survival, particularly during the early brood-rearing period and, therefore, sage-grouse populations may benefit from a management strategy that attempts to increase arthropod abundance via brood habitat management.     

Factors Affecting Nest Survival of Greater Sage-Grouse in Northcentral Montana

Abstract: We studied greater sage-grouse (Centrocercus urophasianus) in northcentral Montana, USA, to examine the relationship between nest success and habitat conditions, environmental variables, and female sage-grouse characteristics. During 2001-2003, we radiomarked 243 female greater sage-grouse, monitored 287 nests, and measured 426 vegetation plots at 4 sites in a 3,200-km² landscape. Nest survival varied with year, grass canopy cover, daily precipitation with a 1-day lag effect, and nesting attempt. In all years, daily survival rate increased on the day of a rain event and decreased the next day. There was temporal variation in nest success both within and among years: success of early (first 28 d of nesting season) nests ranged from 0.238 (SE = 0.080) in 2001 to 0.316 (SE = 0.055) in 2003, whereas survival of late (last 28 d of nesting season) nests ranged from 0.276 (SE = 0.090) in 2001 to 0.418 (SE = 0.055) in 2003. Renests experienced higher survival than first nests. Grass cover was the only important model term that could be managed, but direction and magnitude of the grass effect varied. Site, shrub and forb canopy cover, and Robel pole reading were less useful predictors of nest success; however, temporal and spatial variation in these habitat covariates was low during our study. We note a marked difference between both values and interpretations of apparent nest success, which have been used almost exclusively in the past, and maximum-likelihood estimates used in our study. Annual apparent nest success (0.46) was, on average, 53% higher than maximum-likelihood estimates that incorporate individual, environmental, and habitat covariates. The difference between estimates was variable (range = +8% to +91%). Management of habitats for nesting sage-grouse should focus on increasing grass cover to increase survival of first nests and contribute to favorable conditions for renesting, which should be less likely if survival of first nests increases.     

Mid-contract management of Conservation Reserve Program grasslands provides benefits for ring-necked pheasant nest and brood survival

Conservation Reserve Program (CRP) fields may provide good habitat for nesting and brood-rearing ring-necked pheasants (Phasianus colchicus) during early stages of succession. But, the success of hens in early successional CRP, relative to late successional CRP and other grassland habitats, has yet to be evaluated. The reproductive period is especially critical for populations of pheasants, and CRP's benefits to hens and chicks may decrease as fields age because of loss of vegetative diversity, decrease in vegetation density, and accumulation of residual litter. During 2005–2006, we evaluated spatial and temporal variation in nest and brood survival for radio-marked hen pheasants in areas of northeastern Nebraska where portions of CRP fields had been recently disced and interseeded (DICRP) with legumes. Nests in DICRP tended to have a higher daily survival rate (0.984; 95% CI: 0.957–0.994) than nests in grasslands (including CRP) that were unmanaged (0.951; 95% CI: 0.941–0.972). The probability of 23-day nest success was 0.696 (95% CI: 0.631–0.762) for DICRP and 0.314 (95% CI: 0.240–0.389) for unmanaged grasslands. Daily brood survival rates varied by habitat type, brood age, and date of hatch. The probability of a brood surviving to day 21 was 0.710 (95% CI: 0.610–0.856). Brood survival rates increased with time spent in DICRP and as the brood aged. Survival decreased as broods spent more time in cropland and peaked seasonally with broods that hatched on 15 June. Brood survival probability, to 21 days, would be reduced to 0.36 (95% CI: 0.100–0.701) if broods in our sample had not used DICRP. We combined nest and brood survival in a productivity model that suggested 2,000 hens, in a landscape with no DICRP, would produce 1,826 chicks, whereas the same hens in a landscape of 100% DICRP would produce 5,398 chicks. Production of first-year roosters more than doubled when hens nested in DICRP. Without DICRP, population growth rates of pheasant populations usually declined; with DICRP, populations stabilized with at annual survival rates of 0.3 or greater. The positive response of nest and brood survival to discing and interseeding CRP provides further evidence that CRP fields must be managed to optimize wildlife benefits. © 2012 The Wildlife Society.     

Response of greater sage-grouse to sagebrush reduction treatments in Wyoming big sagebrush

Vegetation treatments have been widely implemented in efforts to enhance conditions for wildlife populations. Yet the effectiveness of such efforts often lack rigorous evaluations to determine whether these practices are effective for targeted species. This is particularly important when manipulating wildlife habitats in ecosystems that are faced with multiple stressors. The sagebrush (Artemisia spp.) ecosystem has been altered extensively over the last century leading to declines of many associated species. Wyoming big sagebrush (A. tridentata wyomingensis) is the most widely distributed subspecies, providing important habitats for sagebrush-obligate and associated wildlife. Sagebrush often has been treated with chemicals, mechanical treatments, and prescribed burning to increase herbaceous forage species released from competition with sagebrush overstory. Despite many studies documenting negative effects of sagebrush control on greater sage-grouse (Centrocercus urophasianus) habitat, treatments are still proposed as a means of improving habitat for sage-grouse and other sagebrush-dependent species. Furthermore, most studies have focused on vegetation response and none have rigorously evaluated the direct influence of these treatments on sage-grouse. We initiated a 9-year (2011–2019) experimental study in central Wyoming, USA, to better understand how greater sage-grouse respond to sagebrush reduction treatments in Wyoming big sagebrush communities. We evaluated the influence of 2 common sagebrush treatments on greater sage-grouse demography and resource selection. We implemented mowing and tebuthiuron application in winter and spring 2014 and evaluated the pre- (2011–2013) and post-treatment (2014–2019) responses of sage-grouse relative to these management actions. We evaluated responses to treatments using demographic and behavioral data collected from 620 radio-marked female greater sage-grouse. Our specific objectives were to evaluate how treatments influenced 1) sage-grouse reproductive success and female survival; 2) sage-grouse nesting, brood-rearing, and female resource selection; 3) vegetation responses; and 4) forbs and invertebrates. Our results generally suggested neutral demographic responses and slight avoidance by greater sage-grouse in response to Wyoming big sagebrush treated by mowing and tebuthiuron. Neither mowing nor tebuthiuron treatments influenced nest survival, brood survival, or female survival. Selection for nest and brood-rearing sites did not differ before and after treatments. Females selected habitats near treatments before and after they were implemented; however, the strength of selection was lower after treatments compared with pre-treatment periods, which may be explained by a lack of response in vegetation and invertebrates following treatments. Perennial grass cover and height varied temporally yet did not vary systematically between treatment and control plots. Forb cover and species richness varied annually but not in relation to either treatment type. Perennial grass cover and height, forb cover, and forb species richness did not increase within mowed or tebuthiuron-treated areas that received 2 or 6 years of grazing rest compared with areas that received no grazing rest. Finally, forb and invertebrate dry mass did not differ between treated plots and control plots at mowing or tebuthiuron sites in any years following treatments. Results from our study add to a large body of evidence that sage-grouse using Wyoming big sagebrush vegetation communities do not respond positively to sagebrush manipulation treatments. Management practices that focus on the maintenance of large, undisturbed tracts of sagebrush will best facilitate the persistence of sage-grouse populations and other species reliant on the sagebrush steppe.     

Assessing Greater Sage-Grouse Selection of Brood-Rearing Habitat Using Remotely-Sensed Imagery: Can Readily Available High-Resolution Imagery Be Used to Identify Brood-Rearing Habitat Across a Broad Landscape?

Greater sage-grouse populations have decreased steadily since European settlement in western North America. Reduced availability of brood-rearing habitat has been identified as a limiting factor for many populations. We used radio-telemetry to acquire locations of sage-grouse broods from 1998 to 2012 in Strawberry Valley, Utah. Using these locations and remotely-sensed NAIP (National Agricultural Imagery Program) imagery, we 1) determined which characteristics of brood-rearing habitat could be used in widely available, high resolution imagery 2) assessed the spatial extent at which sage-grouse selected brood-rearing habitat, and 3) created a predictive habitat model to identify areas of preferred brood-rearing habitat. We used AIC model selection to evaluate support for a list of variables derived from remotely-sensed imagery. We examined the relationship of these explanatory variables at three spatial extents (45, 200, and 795 meter radii). Our top model included 10 variables (percent shrub, percent grass, percent tree, percent paved road, percent riparian, meters of sage/tree edge, meters of riparian/tree edge, distance to tree, distance to transmission lines, and distance to permanent structures). Variables from each spatial extent were represented in our top model with the majority being associated with the larger (795 meter) spatial extent. When applied to our study area, our top model predicted 75% of naïve brood locations suggesting reasonable success using this method and widely available NAIP imagery. We encourage application of our methodology to other sage-grouse populations and species of conservation concern.     

Managing multiple vital rates to maximize greater sage-grouse population growth

Despite decades of field research on greater sage-grouse, range-wide demographic data have yet to be synthesized into a sensitivity analysis to guide management actions. We reviewed range-wide demographic rates for greater sage-grouse from 1938 to 2011 and used data from 50 studies to parameterize a 2-stage, female-based population matrix model. We conducted life-stage simulation analyses to determine the proportion of variation in population growth rate (λ) accounted for by each vital rate, and we calculated analytical sensitivity, elasticity, and variance-stabilized sensitivity to identify the contribution of each vital rate to λ. As expected for an upland game bird, greater sage-grouse showed marked annual and geographic variation in several vital rates. Three rates were demonstrably important for population growth: female survival, chick survival, and nest success. Female survival and chick survival, in that order, had the most influence on λ per unit change in vital rates. However, nest success explained more of the variation in λ than did the survival rates. In lieu of quantitative data on specific mortality factors driving local populations, we recommend that management efforts for greater sage-grouse first focus on increasing female survival by restoring large, intact sagebrush-steppe landscapes, reducing persistent sources of human-caused mortality, and eliminating anthropogenic habitat features that subsidize species that prey on juvenile, yearling, and adult females. Our analysis also supports efforts to increase chick survival and nest success by eliminating anthropogenic habitat features that subsidize chick and nest predators, and by managing shrub, forb, and grass cover, height, and composition to meet local brood-rearing and nesting habitat guidelines. We caution that habitat management to increase chick survival and nest success should not reduce the cover or height of sagebrush below that required for female survival in other seasons (e.g., fall, winter). The success or failure of management actions for sage-grouse should be assessed by measuring changes in vital rates over long time periods to avoid confounding with natural, annual variation. © 2011 The Wildlife Society.     

Lesser Scaup Nest Success and Duckling Survival on the Yukon Flats,Alaska

Abstract: Over the last 20 years scaup numbers have declined, and these declines have been greatest in the northern boreal forests of Canada and Alaska where most lesser scaup (Aythya affinis) nest. We studied nest success and duckling survival of lesser scaup over 3 field seasons, 2001–2003, on the Yukon Flats National Wildlife Refuge in northeastern Alaska, USA. Daily survival rate (DSR) of nests on our study area across all 3 years was 0.943 (n = 177 nests, 95% CI: 0.930–0.954), corresponding to a nest success of only 12.3%, considerably lower than published estimates of an average nest success as high as 57% for lesser scaup in the northern boreal forest. With Mayfield logistic regression, we investigated effects on nest survival of year, clutch initiation date, and nesting habitat type (large wetlands >10 ha, small wetlands <10 ha, and wooded creeks). Neither year nor clutch initiation date influenced nest survival; however, the odds of nest success on large wetlands was 49% lower than on wooded creeks (odds ratio = 0.512, 95% CI = 0.286, 0.918). Based on the model that used only habitat type for estimation, DSR on large wetlands was 0.931 (corresponding nest success = 7.6%), DSR on small wetlands was 0.941 (nest success = 11.1%), and DSR on wooded creeks was 0.963 (nest success = 26.2%). To estimate duckling survival, we monitored 10 broods (n = 75 ducklings) over 3 field seasons by radiotagging hens at nest hatch. Most duckling mortality (94%) occurred in the first 10 days after hatch. Average duckling survival during 1–10 days was 0.321 (95% CI: 0.122–0.772), during 11–20 days was 0.996 (95% CI: 0.891–1.040), and during 21–30 days was 0.923 (95% CI: 0.769–1.041). Three of 10 hens moved all or part of their broods overland between nesting and brood-rearing wetlands for distances of 0.3–1.6 km. Our estimates of lesser scaup nest success and duckling survival on the Yukon Flats were among the lowest ever reported for ducks nesting at northern latitudes, even though the study site was in pristine boreal forest. Estimating and comparing scaup demographic rates from different geographic areas can contribute to improved conservation. Given the scarcity of information on scaup nesting in the boreal forest, basic nesting parameters are important to those trying to model scaup population dynamics.     

Identifying and prioritizing greater sage-grouse nesting and brood-rearing habitat for conservation in human-modified landscapes

Background

Balancing animal conservation and human use of the landscape is an ongoing scientific and practical challenge throughout the world. We investigated reproductive success in female greater sage-grouse (Centrocercus urophasianus) relative to seasonal patterns of resource selection, with the larger goal of developing a spatially-explicit framework for managing human activity and sage-grouse conservation at the landscape level.

Methodology/Principal Findings

We integrated field-observation, Global Positioning Systems telemetry, and statistical modeling to quantify the spatial pattern of occurrence and risk during nesting and brood-rearing. We linked occurrence and risk models to provide spatially-explicit indices of habitat-performance relationships. As part of the analysis, we offer novel biological information on resource selection during egg-laying, incubation, and night. The spatial pattern of occurrence during all reproductive phases was driven largely by selection or avoidance of terrain features and vegetation, with little variation explained by anthropogenic features. Specifically, sage-grouse consistently avoided rough terrain, selected for moderate shrub cover at the patch level (within 90 m²), and selected for mesic habitat in mid and late brood-rearing phases. In contrast, risk of nest and brood failure was structured by proximity to anthropogenic features including natural gas wells and human-created mesic areas, as well as vegetation features such as shrub cover.

Conclusions/Significance

Risk in this and perhaps other human-modified landscapes is a top-down (i.e., human-mediated) process that would most effectively be minimized by developing a better understanding of specific mechanisms (e.g., predator subsidization) driving observed patterns, and using habitat-performance indices such as those developed herein for spatially-explicit guidance of conservation intervention. Working under the hypothesis that industrial activity structures risk by enhancing predator abundance or effectiveness, we offer specific recommendations for maintaining high-performance habitat and reducing low-performance habitat, particularly relative to the nesting phase, by managing key high-risk anthropogenic features such as industrial infrastructure and water developments.     

Greater sage-grouse habitat function relative to 230-kV transmission lines

Greater sage-grouse (Centrocercus urophasianus) is a landscape-level species that requires large tracts of intact sagebrush (Artemisia spp.). Loss of functional habitat resulting from increased demand for energy generation, transmission, and distribution within greater sage-grouse habitats in the western United States has the potential to negatively affect this species. We monitored 346 radio-marked female greater sage-grouse from 2009 to 2014 to evaluate the potential effects of 27-m-tall, 230-kilovolt (kV) wood-pole, H-frame transmission lines on greater sage-grouse habitat selection and demography. We modeled the effect of the transmission lines in 2 different study areas simultaneously using consistent habitat data. Previous research in our study areas suggested that the effect of transmission lines was potentially confounded by other habitat features. We accounted for these potential confounding effects by estimating habitat suitability before estimating the effect of transmission lines. We combined habitat selection and demography results to estimate habitat function relative to transmission lines and inform management recommendations. Overall, we found evidence that transmission lines had a negative effect on greater sage-grouse habitat selection and survival within our study areas over 6 years, but the magnitude of this effect varied by habitat suitability and proximity to occupied leks. The effect of transmission lines on habitat function extended 1.0 km from a transmission line in habitats within 3.1 km of an occupied lek compared to 0.50 km from a transmission line in habitats beyond 3.1 km from occupied leks. Based on these results, we suggest future power line placement relative to sage-grouse nesting, brood-rearing, and summer habitats consider potential effects to sage-grouse habitat selection and demography. Effects can be minimized by incorporating design features that discourage avian predator perching and siting power lines in habitats with lower suitability and, in our study area, habitats beyond 3.1 km from occupied leks. © 2019 The Wildlife Society.     

Behavior and Movement of Wild Turkey Broods

Behavioral and movement ecology of broods are among the most poorly understood aspects of wild turkey (Meleagris gallopavo) reproductive ecology. Recent declines in wild turkey productivity throughout the southeastern United States necessitate comprehensive evaluations of brood ecology across multiple spatial scales. We captured and marked 408 female wild turkeys with global positioning system (GPS)-transmitters across 9 pine (Pinus spp.)-dominated study sites in the southeastern United States during 2014–2019. We evaluated various aspects of the behavioral and movement ecology of 94 brood-rearing females until brood failure or 28 days after hatch (i.e., when poults are classified as juveniles). We found that 34 (36.2%) females had broods (≥1 poult) survive to 28 days after hatch. Broods moved >500 m away from nest sites the day after hatching, and then moved progressively farther away from nest sites over time. Daily movements increased markedly the first 3 days after hatching, and broods moved >1,000 m/day on average thereafter. Females roosted broods an average of 202 m away from nest sites the first night after hatching, but distances between consecutive ground or tree roosts were variable thereafter. Daily core areas increased from 0.8 ha the day of hatch to 4.6 ha by day 28, and range sizes increased from 6.9 ha to 27.9 ha by day 28. Broods tended to consistently select open land cover types, whereas selection for other land cover types varied temporally after hatch day. Broods spent 89% of their time foraging. Predicted daily survival for broods decreased rapidly with increasing distance moved during the initial 3 days after hatching and showed less variation during the subsequent 2 weeks post-hatch. Our findings parallel previous researchers noting that the most critical period for brood survival is the first week after hatch day. Previous researchers have attempted to identify vegetative communities used by broods under the assumption that these communities are a primary factor influencing brood success; however, our results suggest that brood survival is influenced by behavioral decisions related to movements during early brooding periods. © 2020 The Wildlife Society.     

Survival of Greater Sage-Grouse Chicks and Broods in the Northern Great Basin

ABSTRACT Reduced annual recruitment because of poor habitat quality has been implicated as one of the causative factors in the range-wide decline of sage-grouse (Centrocercus urophasianus) populations since the 1950s. Because chick and brood survival are directly linked to annual recruitment and may be the primary factors that limit sage-grouse population growth, we estimated 28-day survival rates of radiomarked chicks and broods from 2000 to 2003. We examined relationships between survival and several habitat variables measured at brood sites, including food availability (insects and forbs); horizontal cover of sagebrush, grasses, and forbs; and vertical cover of sagebrush and grass. We monitored 506 radiomarked chicks from 94 broods; chick survival was 0.392 (SE = 0.024). We found evidence that both food and cover variables were positively associated with chick survival, including Lepidoptera availability, slender phlox (Phlox gracilis) frequency, total forb cover, and grass cover. The effect of total grass cover on chick survival was dependent on the proportion of short grass. The hazard of an individual chick's death decreased 8.6% (95% CI = −1.0 to 18.3) for each percentage point increase in total grass cover when the proportion of short grass was >70%. Survival of 83 radiomarked broods was 0.673 (SE = 0.055). Lepidoptera availability and slender phlox frequency were the only habitat variables related to brood survival. Risk of total brood loss decreased by 11.8% (95% CI = 1.2–22.5) for each additional Lepidoptera individual and 2.7% (95% CI = −0.4 to 5.8) for each percentage point increase in the frequency of slender phlox found at brood sites. Model selection results revealed that temporal differences in brood survival were associated with variation in the availability of Lepidoptera and slender phlox. Years with high brood survival corresponded with years of high Lepidoptera availability and high slender phlox frequency. These foods likely provided high-quality nutrition for chicks during early growth and development and enhanced survival. Habitat management that promotes Lepidoptera and slender phlox abundance during May and June (i.e., early brood rearing) should have a positive effect on chick and brood survival in the short term and potentially increase annual recruitment.     

Greater Sage-Grouse Winter Habitat Selection and Energy Development

Abstract Recent energy development has resulted in rapid and large-scale changes to western shrub-steppe ecosystems without a complete understanding of its potential impacts on wildlife populations. We modeled winter habitat use by female greater sage-grouse (Centrocercus urophasianus) in the Powder River Basin (PRB) of Wyoming and Montana, USA, to 1) identify landscape features that influenced sage-grouse habitat selection, 2) assess the scale at which selection occurred, 3) spatially depict winter habitat quality in a Geographic Information System, and 4) assess the effect of coal-bed natural gas (CBNG) development on winter habitat selection. We developed a model of winter habitat selection based on 435 aerial relocations of 200 radiomarked female sage-grouse obtained during the winters of 2005 and 2006. Percent sagebrush (Artemisia spp.) cover on the landscape was an important predictor of use by sage-grouse in winter. The strength of habitat selection between sage-grouse and sagebrush was strongest at a 4-km² scale. Sage-grouse avoided coniferous habitats at a 0.65-km² scale and riparian areas at a 4-km² scale. A roughness index showed that sage-grouse selected gentle topography in winter. After controlling for vegetation and topography, the addition of a variable that quantified the density of CBNG wells within 4 km² improved model fit by 6.66 Akaike's Information Criterion points (Akaike wt = 0.965). The odds ratio for each additional well in a 4-km² area (0.877; 95% CI = 0.834- 0.923) indicated that sage-grouse avoid CBNG development in otherwise suitable winter habitat. Sage-grouse were 1.3 times more likely to occupy sagebrush habitats that lacked CBNG wells within a 4-km² area, compared to those that had the maximum density of 12.3 wells per 4 km² allowed on federal lands. We validated the model with 74 locations from 74 radiomarked individuals obtained during the winters of 2004 and 2007. This winter habitat model based on vegetation, topography, and CBNG avoidance was highly predictive (validation R² = 0.984). Our spatially explicit model can be used to identify areas that provide the best remaining habitat for wintering sage-grouse in the PRB to mitigate impacts of energy development.     

Interactions between common buzzard Buteo buteo and goshawk Accipiter gentilis: trade-offs revealed by a field experiment

I examined the behavioural interactions between common buzzard Buteo buteo and goshawk Accipiter gentilis and their effects on buzzard breeding success and brood defence with a two-year field experiment using dummies and playback calls. A priori I showed through an extensive nest site analysis that there is considerable nesting habitat overlap between the two species and hence potential for interspecific competition for prime nesting habitat. Buzzards had a significantly lower breeding success when presented with a goshawk dummy compared to control broods but there was no effect of buzzard dummies on reproductive success. Buzzards failing with their breeding attempt tended to select another nest site while successful buzzards more frequently used the same nest again. Buzzard pairs were less often attacked by common crows Corvus corone while exposed to goshawk dummies compared to buzzard dummies. The decision to desert a nest seems to be a trade-off between predation risk on the one hand and protection against crows on the other. Goshawks proved far more aggressive against an intraspecific dummy than buzzards. Buzzards adjusted their level of brood defence against both intra- and interspecific dummies according to the age of offspring but not offspring number, with an increasing brood defence level with increasing offspring age. Thus the behaviour of buzzards towards goshawks is a result of a complex system of trade-offs between predation risk, competition for prime nesting habitat and protection from crows on which brood value acts as a temporal modifier.     

Recovery of Greater Sage-Grouse Habitat Features in Wyoming Big Sagebrush following Prescribed Fire

The ability of prescribed fire to enhance habitat features for Greater Sage-Grouse ( Centrocercus urophasianus ) in Wyoming big sagebrush ( Artemisia tridentata wyomingensis ) in western North America is poorly understood. We evaluated recovery of habitat features important to wintering, nesting, and early brood-rearing Sage-Grouse in Wyoming big sagebrush following prescribed fire. Our case study included 1 year of preburn (1989) and 10 years of postburn data collected over 14 years (1990–2003) from control and burned study areas in the Big Desert of southeastern Idaho, U.S.A. We compared recovery and rate of change for 12 features in four categories between burned and control transects and recovery in burned transects including change in variation. Our results indicate that prescribed fire induced quantifiable changes in wintering, nesting, and early brood-rearing Sage-Grouse habitat features 14 years after fire in Wyoming big sagebrush in our study area. Specifically, grass and litter required by Sage-Grouse for nest and brood concealment recovered relatively rapidly following fire; major forb cover was similar between burned and control sites, but the rate of increase for major forb cover and richness was greater in control transects, and structurally mediated habitat features required by Sage-Grouse for food and cover in winter and for nest and brood concealment in spring recovered slowly following fire. Because shrub structural features in our study did not recover in magnitude or variability to preburn levels 14 years after fire, we recommend that managers avoid burning Wyoming big sagebrush to enhance Sage-Grouse habitat, but rather implement carefully planned treatments that maintain Sagebrush.     

Survival of Wood Duck Ducklings and Broods in Mississippi and Alabama

ABSTRACT Although North American wood ducks (Aix sponsa) are well-studied throughout their range, researchers know little about demographic and environmental factors influencing survival of ducklings and broods, which is necessary information for population management. We studied radiomarked female and duckling wood ducks that used nest boxes and palustrine wetlands at Noxubee National Wildlife Refuge (NNWR) in Mississippi, USA, in 1996–1999, and riverine wetlands of the Tennessee-Tombigbee Rivers and Waterway (TTRW) system in Alabama in 1998–1999. We estimated survival of ducklings and broods and evaluated potentially important predictors of duckling survival, including age and body mass of brood-rearing females, hatch date of ducklings, duckling mass, brood size at nest departure, inter-day travel distance by ducklings, site and habitat use, and daily minimum air temperature and precipitation. At NNWR, survival of 300 radiomarked ducklings ranged from 0.15 (95% CI = 0.04-0.27) to 0.24 (95% CI = 0.13-0.38) and was 0.21 (95% CI = 0.15-0.28) for 1996–1999. Our overall estimate of brood survival was 0.64 (n = 91; 95% CI = 0.54-0.73). At TTRW, survival of 129 radiomarked ducklings was 0.29 in 1998 (95% CI = 0.20-0.41) and 1999 (95% CI = 0.13-0.45) and was 0.29 (95% CI = 0.20-0.40) for 1998–1999. Our overall estimate of brood survival was 0.71 (n = 38; 95% CI = 0.56-0.85). At NNWR, models that included all predictor variables best explained variation in duckling survival. Akaike weight (w_i) for the best model was 0.81, suggesting it was superior to other models (<0.01 < w_i < 0.18). We detected 4 competing models for duckling survival at TTRW. Inter-day distance traveled by ducklings was important as this variable appeared in all 4 models; duckling survival was positively related to this variable. Patterns of habitat-related survival were similar at both study areas. Ducklings in broods that used scrub-shrub habitats disjunct from wetlands containing aggregations of nest boxes had greater survival probabilities than birds remaining in wetlands with such nest structures. Managers may increase local wood duck recruitment by promoting availability of suitable brood habitats (e.g., scrub-shrub wetlands) without aggregations of nest boxes that may attract predators and by dispersing nest boxes amid or adjacent to these habitats. We did not determine an optimal density of nest boxes relative to local or regional population goals, which remains important research and conservation needs.     

Columbian sharp-tailed grouse female and nest survival in northwestern Colorado

Wildlife management and conservation can be challenging when the demography of a focal species is unknown or limited given that fecundity and adult survival influence population growth. The Columbian sharp-tailed grouse (Tympanuchus phasianellus columbianus) have been reduced to ≤10% of their former range since the early 1900s. We conducted a 3-year study (2015–2017) across 4 study sites in northwestern Colorado, USA, to evaluate female hazard and nest survival. We trapped and marked 270 female sharp-tailed grouse and identified 275 nests for our hazard and survival analyses. Females during the breeding stage of the reproductive season experienced more hazard compared to the nesting and the early and late post-nesting stages for females without broods. Females experienced a higher degree of hazard during the breeding stage and mortality risk was >3 times higher than the nesting stage, >7 times higher than early post-nesting (EPN)-no brood stage, and >5 times higher than the late post-nesting (LPN)-unsuccessful stage. Two reproductive season stages (LPN-successful and EPN-brood) provided marginal inference. Nest incubation initiation date and nest age best described nest daily survival. Females that initiated incubation of initial nests earlier in the season experienced lower nest daily survival than later in the incubation season. Because female Columbian sharp-tailed grouse hazard varied among different reproductive season stages, we recommend that wildlife managers develop management actions that reduce hazard during the specific reproductive season stages (i.e., the breeding season). For Columbian sharp-tailed grouse in Colorado, we recommend that Colorado Parks and Wildlife collaborate with federal farm program agencies to implement a no-tillage restriction from 1 May through 30 June for active agricultural fields within 2 km of active Columbian sharp-tailed grouse leks to enhance nest survival.     

Piping plover chick ecology following landscape-level disturbance

Population declines of disturbance-dependent species due to suppression of natural disturbances are realized across ecosystems. The piping plover (Charadrius melodus; plover), a disturbance-dependent and conservation-reliant shorebird that nests on sandy beaches and barrier islands on the Atlantic Coast, was listed under the United States Endangered Species Act in 1986. In 2012, Hurricane Sandy landed on Fire and Westhampton islands, barrier island nesting sites for plovers in New York, USA. Hurricane Sandy was a natural disturbance in this system, creating abundant nesting habitat. The number of chicks produced by a pair, or a population, is a direct measure of reproductive output, and gaining a better understanding of productivity and chick behavior following large-scale habitat creation may improve plover habitat management and potentially species persistence. We evaluated the effects of landscape features on habitat selection, behavior, and survival of plover broods using logistic regression, generalized linear mixed effects models, and survival models. Plover broods selected flatter sites with less dense vegetation than available at random. Chick foraging rates were highest in moist substrates and were lower in areas of higher nesting plover density. Chick survival was greater for broods that hatched earlier in the breeding season and increased as chicks aged. Generally, providing access to sites with flatter, moist substrates will likely result in higher quality brood rearing habitat on the landscape. Ultimately, vegetation removal and habitat management may be needed to reduce plover nesting density and ensure sufficient habitat, which may in turn improve plover chick survival. Moreover, sustaining natural landscape disturbances such as those resulting from storms, and not taking actions to prevent hurricane-created overwash, will allow these landscape features to persist.     

Nest Predation of Greater Sage-Grouse in Relation to Microhabitat Factors and Predators

ABSTRACT Nest predation is a natural component of greater sage-grouse (Centrocercus urophasianus) reproduction, but changes in nesting habitat and predator communities may adversely affect grouse populations. We used a 2-part approach to investigate sage-grouse nest predation. First, we used information criteria to compare nest survival models that included indices of common raven (Corvus corax) abundance with other survival models that consisted of day of incubation, grouse age, and nest microhabitat covariates using measurements from 77 of 87 sage-grouse nests. Second, we used video monitoring at a subsample of 55 of 87 nests to identify predators of depredated nests (n = 16) and evaluated the influence of microhabitat factors on the probability of predation by each predator species. The most parsimonious model for nest survival consisted of an interaction between day of incubation and abundance of common ravens (w_{ravenXincubation day} = 0.67). An estimated increase in one raven per 10-km transect survey was associated with a 7.4% increase in the odds of nest failure. Nest survival was relatively lower in early stages of incubation, and this effect was strengthened with increased raven numbers. Using video monitoring, we found the probability of raven predation increased with reduced shrub canopy cover. Also, we found differences in shrub canopy cover and understory visual obstruction between nests depredated by ravens and nests depredated by American badgers (Taxidea taxus). Increased raven numbers have negative effects on sage-grouse nest survival, especially in areas with relatively low shrub canopy cover. We encourage wildlife managers to reduce interactions between ravens and nesting sage-grouse by managing raven populations and restoring and maintaining shrub canopy cover in sage-grouse nesting areas.     

Interseasonal movements of greater sage-grouse,migratory behavior,and an assessment of the core regions concept in Wyoming

Animals can require different habitat types throughout their annual cycles. When considering habitat prioritization, we need to explicitly consider habitat requirements throughout the annual cycle, particularly for species of conservation concern. Understanding annual habitat requirements begins with quantifying how far individuals move across landscapes between key life stages to access required habitats. We quantified individual interseasonal movements for greater sage-grouse (Centrocercus urophasianus; hereafter sage-grouse) using radio-telemetry spanning the majority of the species distribution in Wyoming. Sage-grouse are currently a candidate for listing under the United States Endangered Species Act and Wyoming is predicted to remain a stronghold for the species. Sage-grouse use distinct seasonal habitats throughout their annual cycle for breeding, brood rearing, and wintering. Average movement distances in Wyoming from nest sites to summer-late brood-rearing locations were 8.1 km (SE = 0.3 km; n = 828 individuals) and the average subsequent distances moved from summer sites to winter locations were 17.3 km (SE = 0.5 km; n = 607 individuals). Average nest-to-winter movements were 14.4 km (SE = 0.6 km; n = 434 individuals). We documented remarkable variation in the extent of movement distances both within and among sites across Wyoming, with some individuals remaining year-round in the same vicinity and others moving over 50 km between life stages. Our results suggest defining any of our populations as migratory or non-migratory is innappropriate as individual strategies vary widely. We compared movement distances of birds marked using Global Positioning System (GPS) and very high frequency (VHF) radio marking techniques and found no evidence that the heavier GPS radios limited movement. Furthermore, we examined the capacity of the sage-grouse core regions concept to capture seasonal locations. As expected, we found the core regions approach, which was developed based on lek data, was generally better at capturing the nesting locations than summer or winter locations. However, across Wyoming the sage-grouse breeding core regions still contained a relatively high percentage of summer and winter locations and seem to be a reasonable surrogate for non-breeding habitat when no other information exists. We suggest that conservation efforts for greater sage-grouse implicitly incorporate seasonal habitat needs because of high variation in the amount of overlap among breeding core regions and non-breeding habitat. © 2012 The Wildlife Society.