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Twenty quadrats within the burn perimeter of a September 2021 wildfire outside of Boise, Idaho were surveyed for the abundance of fire effects, biocrusts and vascular plants immediately post-fire. The fire was too small to be named. Char was measured as a proxy for fire intensity. Biocrusts were surveyed by morphogroup (crustose lichens, cup lichens, fruticose lichens, gelatinous lichens, short moss, tall moss) and vascular plants were surveyed by functional group (annual forbs, perennial grasses). Char was measured ocularly and biocrust/plant abundance was measured via point-vertex intercept at 40 points per quadrat. These data support the following publication: Condon, L.A., Shinneman, D.J., Rosentreter, R. and...
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We used a hierarchical Bayesian modeling framework to estimate resource selection functions and survival for early and late brood-rearing stages of sage-grouse in relation to a broad suite of habitat characteristics evaluated at multiple spatial scales within the Great Basin from 2009 to 2019. Sage-grouse selected for greater perennial grass cover, higher relative elevations, and areas closer to springs and wet meadows during both early and late brood-rearing. Terrain characteristics, including heat load and aspect, were important in survival models, as was variation in shrub height. We also found strong evidence for higher survival for both early and late broods within previously burned areas, but survival within...
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Predicted common raven (Corvus corax) impacts within greater sage-grouse (Centrocercus urophasianus) concentration areas across the Great Basin, USA, 2007–2016. Predicted impacts were based on a raven density of great than or equal to 0.40 (ravens per square kilometer) which corresponded to below-average survival rates of sage-grouse nests. These data support the following publication: Coates, P.S., O'Neil, S.T., Brussee, B.E., Ricca, M.A., Jackson, P.J., Dinkins, J.B., Howe, K.B., Moser, A.M., Foster, L.J. and Delehanty, D.J., 2020. Broad-scale impacts of an invasive native predator on a sensitive native prey species within the shifting avian community of the North American Great Basin. Biological Conservation,...
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Average and standard deviation of annual predicted common raven (Corvus corax) density (ravens per square kilometer) derived from random forest models given field site unit-specific estimates of raven density that were obtained from hierarchical distance sampling models at 43 field site units within the Great Basin region, USA. Fifteen landscape-level predictors summarizing climate, vegetation, topography and anthropogenic footprint were used to predict average raven density at each unit. These data support the following publication: Coates, P.S., O'Neil, S.T., Brussee, B.E., Ricca, M.A., Jackson, P.J., Dinkins, J.B., Howe, K.B., Moser, A.M., Foster, L.J. and Delehanty, D.J., 2020. Broad-scale impacts of an invasive...
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We evaluated the expected success of habitat recovery in priority areas under 3 different restoration scenarios: passive, planting, and seeding. Passive means no human intervention following a fire disturbance. Under a planting scenario, field technicians methodically plant young sagebrush saplings at the burned site. The seeding scenario involves distributing large amounts of sagebrush seeds throughout the affected area.
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Monitoring change in genetic diversity in wildlife populations across multiple scales could facilitate prioritization of conservation efforts. We used microsatellite genotypes from 7,080 previously collected genetic samples from across the greater sage-grouse (Centrocercus urophasianus) range to develop a modelling framework for estimating genetic diversity within a recently developed hierarchically nested monitoring framework (clusters). The majority of these genetic samples (n=6560) were used in previous research (Oyler-McCance et al. 2014; Cross et. al 2018; Row et. al. 2018). Genetic diversity values associated with clusters across multiple scales could facilitate the identification of areas with low genetic...
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Predictions of raven occurrence in the absence of anthropogenic environmental effects. Raven point counts were related to landscape covariates using Bayesian hierarchical occupancy models and the means of the posterior distributions for relevant effects were used to generate the predictions.
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Map of cumulative 38-day nest survival predicted from a Bayesian hierarchical shared frailty model of sage-grouse nest fates. The midpoint of coefficient conditional posterior distributions of 38-day nest survival were used for prediction at each 30 meter pixel across the landscape.
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These data represent predicted common raven (Corvus corax) density (ravens/square-km) derived from random forest models given field site unit-specific estimates of raven density that were obtained from hierarchical distance sampling models at 43 field site units within the Great Basin region, USA. Fifteen landscape-level predictors summarizing climate, vegetation, topography and anthropogenic footprint were used to predict average raven density at each unit. A raven density of greater than or equal to 0.40 ravens/square-km corresponds to below-average survival rates of sage-grouse (Centrocercus urophasianus) nests. We mapped areas which exceed this threshold within sage-grouse concentration areas to determine where...
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We evaluated brood-rearing habitat selection and brood survival of greater sage-grouse (Centrocercus urophasianus; hereafter, sage-grouse) in Long Valley, California, an area where the water rights are primarily owned by the city of Los Angeles and water is used locally to irrigate for livestock. This area thus represents a unique balance between the needs of wildlife and people that could increasingly define future water management. In this study, sage-grouse broods moved closer to the edge of mesic areas and used more interior areas during the late brood-rearing period, selecting for greener areas after 1 July. Mesic areas were particularly important during dry years, with broods using areas farther interior than...
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We evaluated nest site selection and nest survival both before and after a fire disturbance occurred. We then combined those surfaces to determine the areas which were most heavily impacted by the fire.
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These data represent habitat selection of greater sage-grouse at the 50 day mark of their brood rearing process. Sage-grouse and their broods were monitored on their own individual time lines, so one group's 50th day may not necessarily be the same as any other bird's 50th day.
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A raster representing Greater Sage-grouse (hereafter sage-grouse) space-use and lek abundance. A higher pixel value corresponds to a greater amount of likelihood that the area is utilized by sage-grouse. Values are the result of combining a kernel density estimation on lek abundances with a raster representing distance to lek. The kernel density was calculated using maximum lek abundances observed between the most recent population nadir for the Great Basin region (2013) and the most recent lek counts available (2021). Polygons representing high-space use areas of Greater Sage-grouse (hereafter sage-grouse) space-use and lek abundance. Areas represent the 85 percent isopleth of the abundance and space-use index...
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Raster layers depicting the distribution of possible ecological traps to sage-grouse based on the intersection of conifer cover-classes 1 (Greater than 0 up to 10 percent) and 2 (11 up to 20 percent) with high resistance and resilience, and ecological traps within sage-grouse concentration areas and ecological traps in sage-grouse habitat.
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These data represent an resource selection function (RSF) for translocated sage-grouse in North Dakota during the summer. Human enterprise has led to large‐scale changes in landscapes and altered wildlife population distribution and abundance, necessitating efficient and effective conservation strategies for impacted species. Greater sage‐grouse (Centrocercus urophasianus; hereafter sage‐grouse) are a widespread sagebrush (Artemisia spp.) obligate species that has experienced population declines since the mid‐1900s resulting from habitat loss and expansion of anthropogenic features into sagebrush ecosystems. Habitat loss is especially evident in North Dakota, USA, on the northeastern fringe of sage‐grouse’ distribution,...
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Predictions of raven occurrence in the absence of natural environmental effects. Raven point counts were related to landscape covariates using Bayesian hierarchical occupancy models and the means of the posterior distributions for relevant effects were used to generate the predictions.
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We monitored Greater Sage-Grouse (Centrocercus urophasianus; hereafter, Sage-Grouse) nests and various habitat characteristics at the nest locations near Susanville in northeastern California, crossing over into northwestern Nevada. We employed a before-after-control-impact (BACI) experimental design to account for spatiotemporal heterogeneity in the system and to derive estimates of relative change in survival parameters. Sage-Grouse nest survival decreased after the Rush Fire but decreased more in the burned area relative to the unburned area. Although female Sage-Grouse continued to occupy burned areas, nest survival was reduced from 52 percent to 19 percent. Using a BACI ratio approach we found that nest survival...
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Ranked index of model-projected nest site selection integrated with nesting productivity (i.e., nest survival), demonstrating the spatial distribution of adaptive vs. maladaptive habitat selection at each 30 m pixel. Hierarchical models of nest selection and survival were fit to landscape covariates within a Bayesian modeling framework in Nevada and California from 2009 through 2017 to develop spatially explicit information about nest site selection and survival consequences across the landscape. Habitat was separated into 16 classes ranking from high (1) to low (16). Habitat ranked highest where the top nest selection and survival classes intersected (adaptive selection), whereas the lowest rank occurred where...


map background search result map search result map Raven study site locations in the Great Basin, derived from survey locations 2007 - 2016 Predictions of raven occurrence in the absence of natural environmental effects in the Great Basin, 2007-2016 (Fig. 4A) Predictions of raven occurrence in the absence of anthropogenic environmental effects in the Great Basin, 2007-2016 (Fig. 4B) Prediction of raven occurrence intersected with high impact areas for sage-grouse populations in the Great Basin, 2007-2016 (Fig. 5A) Possible Ecological Traps to Sage-grouse in the Bistate Region of California and Nevada Data Maps of Predicted Raven Density and Areas of Potential Impact to Nesting Sage-grouse within Sagebrush Ecosystems of the North American Great Basin Raven Impacts within Greater Sage-grouse Concentration Areas within the Great Basin Region of the United States 2007 - 2016 Average and Standard Deviation of Annual Predicted Raven Density in the Great Basin, Western U.S. Greater Sage-grouse Nest Survival, Nevada and California 2019 Greater Sage-grouse Nest Site Source-Sink, Nevada and California 2019 Summer RSF of Translocated Greater Sage-grouse in North Dakota, 2017 - 2018 Genotypes and cluster definitions for a range-wide greater sage-grouse dataset collected 2005-2017 (ver 1.1, January 2023) Greater Sage-Grouse Nest Observations Before and After Wildfire Disturbance in Northeastern California (2007-2018) Fire Response Effects, Biocrust, and Vascular Plant Abundance Following Wildfire near Boise, Idaho (October 2021) Spatially-Explicit Predictive Maps of Greater Sage-Grouse Brood Selection Integrated with Brood Survival in Nevada and Northeastern California, USA Habitat Suitability Index for Greater Sage-Grouse 50 Days into the Brood Rearing Life Stage, Nevada and California Sagebrush Restoration Under Passive, Planting, and Seeding Scenarios Following Fire Disturbance in the Virginia Mountains, Nevada (2018) Post-Fire Change in Greater Sage-Grouse Nest Selection and Survival in the Virginia Mountains, Nevada (2018) Selection and Survival of Greater Sage-Grouse Broods in Mesic Areas of Long Valley, California (2003 - 2018) Greater Sage-grouse Abundance and Space-use Index, Nevada and Northeastern California Selection and Survival of Greater Sage-Grouse Broods in Mesic Areas of Long Valley, California (2003 - 2018) Post-Fire Change in Greater Sage-Grouse Nest Selection and Survival in the Virginia Mountains, Nevada (2018) Sagebrush Restoration Under Passive, Planting, and Seeding Scenarios Following Fire Disturbance in the Virginia Mountains, Nevada (2018) Fire Response Effects, Biocrust, and Vascular Plant Abundance Following Wildfire near Boise, Idaho (October 2021) Greater Sage-Grouse Nest Observations Before and After Wildfire Disturbance in Northeastern California (2007-2018) Summer RSF of Translocated Greater Sage-grouse in North Dakota, 2017 - 2018 Possible Ecological Traps to Sage-grouse in the Bistate Region of California and Nevada Greater Sage-grouse Nest Site Source-Sink, Nevada and California 2019 Greater Sage-grouse Nest Survival, Nevada and California 2019 Greater Sage-grouse Abundance and Space-use Index, Nevada and Northeastern California Spatially-Explicit Predictive Maps of Greater Sage-Grouse Brood Selection Integrated with Brood Survival in Nevada and Northeastern California, USA Habitat Suitability Index for Greater Sage-Grouse 50 Days into the Brood Rearing Life Stage, Nevada and California Raven study site locations in the Great Basin, derived from survey locations 2007 - 2016 Raven Impacts within Greater Sage-grouse Concentration Areas within the Great Basin Region of the United States 2007 - 2016 Prediction of raven occurrence intersected with high impact areas for sage-grouse populations in the Great Basin, 2007-2016 (Fig. 5A) Data Maps of Predicted Raven Density and Areas of Potential Impact to Nesting Sage-grouse within Sagebrush Ecosystems of the North American Great Basin Average and Standard Deviation of Annual Predicted Raven Density in the Great Basin, Western U.S. Predictions of raven occurrence in the absence of natural environmental effects in the Great Basin, 2007-2016 (Fig. 4A) Predictions of raven occurrence in the absence of anthropogenic environmental effects in the Great Basin, 2007-2016 (Fig. 4B) Genotypes and cluster definitions for a range-wide greater sage-grouse dataset collected 2005-2017 (ver 1.1, January 2023)