USGS ScienceSearch

Geology topics

Steven E. Hanser

Publications and source records attributed to Steven E. Hanser.

29 records · Page 2Linked to original sources

Dose-Response Calculator for ArcGIS

The Dose-Response Calculator for ArcGIS is a tool that extends the Environmental Systems Research Institute (ESRI) ArcGIS 10 Desktop application to aid with the visualization of relationships between two raster GIS datasets. A dose-response curve is a line graph commonly used in medical research to examine the effects of different dosage rates of a drug or chemical (for example, carcinogen) on an outcome of interest (for example, cell mutations) (Russell and others, 1982). Dose-response curves have recently been used in ecological studies to examine the influence of an explanatory dose variable (for example, percentage of habitat cover, distance to disturbance) on a predicted response (for example, survival, probability of occurrence, abundance) (Aldridge and others, 2008). These dose curves have been created by calculating the predicted response value from a statistical model at different levels of the explanatory dose variable while holding values of other explanatory variables constant. Curves (plots) developed using the Dose-Response Calculator overcome the need to hold variables constant by using values extracted from the predicted response surface of a spatially explicit statistical model fit in a GIS, which include the variation of all explanatory variables, to visualize the univariate response to the dose variable. Application of the Dose-Response Calculator can be extended beyond the assessment of statistical model predictions and may be used to visualize the relationship between any two raster GIS datasets (see example in tool instructions). This tool generates tabular data for use in further exploration of dose-response relationships and a graph of the dose-response curve.

Data Series

Greater sage-grouse as an umbrella species for shrubland passerine birds: a multiscale assessment

Working groups and government agen-cies are planning and conducting land actions in sagebrush (Artemisia spp.) habitats to benefit Greater Sage-Grouse (Centrocercus urophasianus) populations. Managers have adopted an umbrella concept, creating habitat characteristics specific to sage-grouse requirements, in the belief that other wildlife species dependent on sagebrush will benefit. We tested the efficacy of this approach by first identifying the primary environmental gradients underlying sagebrush steppe bird com-munities (including Greater Sage-Grouse). We integrated field sampling for birds and vegetation with geographic information system (GIS) data to characterize 305 sites sampled throughout the current range of Greater Sage-Grouse in the Intermountain West, United States. The primary environmental axis defining the bird community represented a gradient from local-scale Wyoming/basin big sagebrush (A. t. ssp. wyomingensis/A. t. ssp. tridentata), and bare ground cover to local and regional grassland cover; the second axis repre-sented a transition from low-elevation Wyoming/basin big sagebrush and bare ground to mountain big sagebrush (A. t. ssp. vaseyana) and habitat edge. We identified the relative overlap of sage-grouse with 13 species of passerine birds along the multiscale gradients and estimated the width of the umbrella when applying management guidelines specific to sage-grouse. Passerine birds associated with sagebrush steppe habitats had high levels of overlap with Greater Sage-Grouse along the multiscale environmental gradients. However, the overlap of the umbrella was prima-rily a function of the broad range of sagebrush habitats used by sage-grouse. Management that focuses on creating a narrow set of plot-scale con-ditions will likely be less effective than restoration efforts that recognize landscape scale heterogene-ity and multiscale organization of habitats. These multiscale efforts may improve some sage-grouse habitats and strengthen the management umb-rella for shrub steppe passerine birds.

Book chapter

Connecting pattern and process in greater sage-grouse populations and sagebrush landscapes

Abstract. Spatial patterns influence the processes that maintain Greater Sage-Grouse (Centrocercus urophasianus) populations and sagebrush (Artemisia spp.) landscapes on which they depend. We used connectivity analyses to: (1) delineate the dominant pattern of sagebrush landscapes; (2) identify regions of the current range-wide distribution of Greater Sage-Grouse important for conservation; (3) estimate distance thresholds that potentially isolate populations; and (4) understand how landscape pattern, environmental disturbance, or location within the spatial network influenced lek persistence during a population decline. Long-term viability of sagebrush, assessed from its dominance in relatively unfragmented landscapes, likely is greatest in south-central Oregon and northwest Nevada; the Owyhee region of southeast Oregon, southwest Idaho, and northern Nevada; southwest Wyoming; and south-central Wyoming. The most important leks (breeding locations) for maintaining connectivity, characterized by higher counts of sage-grouse and connections with other leks, were within the core regions of the sage-grouse range. Sage-grouse populations presently have the highest levels of connectivity in the Wyoming Basin and lowest in the Columbia Basin Sage-Grouse management zones (SMZs). Leks separated by distances 13-18 km could be isolated due to decreased probability of dispersals from neighboring leks. The range-wide distribution of sage-grouse was clustered into 209 separate components (units in which leks were interconnected within but not among) when dispersal was limited to distances 18 km. The most important components for maintaining connectivity were distributed across the central and eastern regions of the range-wide distribution. Connectivity among sage-grouse populations was lost during population declines from 1965-1979 to 1998-2007, most dramatically in the Columbia Basin SMZ. Leks that persisted during this period were larger in size, were more highly connected, and had lower levels of broad-scale fire and human disturbance. Protecting core regions and maintaining connectivity with more isolated sage-grouse populations may help reverse or stabilize the processes of range contraction and isolation that have resulted in long-term population declines.

Book chapter

Influences of environmental and anthropogenic features on greater sage-grouse populations, 1997-2007

The Greater Sage-Grouse (Centrocercus urophasianus), endemic to western North Amer-ica, is of great conservation interest. Its popula-tions are tracked by spring counts of males at lek sites. We explored the relations between trends of Greater Sage-Grouse lek counts from 1997 to 2007 and a variety of natural and anthropogenic fea-tures. We found that trends were correlated with several habitat features, but not always similarly throughout the range. Lek trends were positively associated with proportion of sagebrush (Artemisia spp.) cover, within 5 km and 18 km. Lek trends had negative associations with the coverage of agriculture and exotic plant species. Trends also tended to be lower for leks where a greater pro-portion of their surrounding landscape had been burned. Few leks were located within 5 km of developed land and trends were lower for those leks with more developed land within 5 km or 18 km. Lek trends were reduced where communi-cation towers were nearby, whereas no effect of power lines was detected. Active oil or natural gas wells and highways, but not secondary roads, were associated with lower trends. Effects of some anthropogenic features may have already been manifested before our study period and thus not have been detected in this analysis. Results of this range-wide analysis complement those from more intensive studies on smaller areas. Our findings are important for identifying features that could threaten Greater Sage-Grouse populations.

Book chapter

Ecological influence and pathways of land use in sagebrush

Land use in sagebrush (Artemisia spp.) landscapes influences all sage-grouse (Centrocer-cus spp.) populations in western North America. Croplands and the network of irrigation canals cover 230,000 km2 and indirectly influence up to 77% of the Sage-Grouse Conservation Area and 73% of sagebrush land cover by subsidizing synanthropic predators on sage-grouse. Urbanization and the demands of human population growth have created an extensive network of con-necting infrastructure that is expanding its influence on sagebrush landscapes. Over 2,500 km 2 are now covered by interstate highways and paved roads; when secondary roads are included, 15% of the Sage-Grouse Conservation Area and 5% of existing sagebrush habitats are 2.5 km from roads. Density of secondary roads often exceeds 5 km/km 2 , resulting in widespread motorized access for recreation, creating extensive travel corridors for management actions and resource development, subsidizing predators adapted to human presence, and facilitating spread of exotic or invasive plants. Sagebrush lands also are being used for their wilderness and recreation values, including off highway vehicle use. Approximately 12,000,000 animal use months (AUM amount of forage to support one livestock unit per month) are permitted for grazing livestock on public lands in the western states. Direct effects of grazing on sage-grouse populations or sagebrush landscapes are not possible to assess from current data. However, management of lands grazed by livestock has influenced sagebrush ecosystems by vegetation treatments to increase forage and reduce sagebrush and other plant species unpalatable to livestock. Fences (2 km/km 2 in some regions), roads, and water developments to manage livestock movements further modify the landscape. Oil and gas development influences 8% of the sagebrush habitats with the highest intensities occurring in the eastern range of sage-grouse; 20% of the sagebrush distribution is indirectly influenced in the Great Plains, Wyoming Basin, and Colorado Plateau SMZs. Energy development physically removes habitat to construct well pads, roads, power lines, and pipelines; indirect effects include habitat fragmentation, soil disturbance, and facilitation of exotic plant and animal spread. More recent development of alternative energy, such as wind and geothermal, creates infrastructure in new regions of the sage-grouse distribution. Land use will continue to be a dominant stressor on sage-brush systems; its individual and cumulative effects will challenge long-term conservation of sage-grouse populations.

Book chapter

Influences of the human footprint on sagebrush landscape patterns: Implications for sage-grouse conservation

Spatial patterns influence the processes that maintain Greater Sage-Grouse (Centrocercus urophasianus) populations and sagebrush (Artemisia spp.) landscapes on which they depend. We used connectivity analyses to: (1) delineate the dominant pattern of sagebrush landscapes; (2) identify regions of the current range-wide distribution of Greater Sage-Grouse important for conservation; (3) estimate distance thresholds that potentially isolate populations; and (4) understand how landscape pattern, environmental disturbance, or location within the spatial network influenced lek persistence during a population decline. Long-term viability of sagebrush, assessed from its dominance in relatively unfragmented landscapes, likely is greatest in south-central Oregon and northwest Nevada; the Owyhee region of southeast Oregon, southwest Idaho, and northern Nevada; southwest Wyoming; and south-central Wyoming. The most important leks (breeding locations) for maintaining connectivity, characterized by higher counts of sage-grouse and connections with other leks, were within the core regions of the sage-grouse range. Sage-grouse populations presently have the highest levels of connectivity in the Wyoming Basin and lowest in the Columbia Basin Sage-Grouse management zones (SMZs). Leks separated by distances 1318 km could be isolated due to decreased probability of dispersals from neighboring leks. The range-wide distribution of sage-grouse was clustered into 209 separate components (units in which leks were interconnected within but not among) when dispersal was limited to distances 18 km. The most important components for maintaining connectivity were distributed across the central and eastern regions of the range-wide distribution. Connectivity among sage-grouse populations was lost during population declines from 1965 1979 to 1998 2007, most dramatically in the Columbia Basin SMZ. Leks that persisted during this period were larger in size, were more highly connected, and had lower levels of broad-scale fire and human disturbance. Protecting core regions and maintaining connectivity with more isolated sage-grouse populations may help reverse or stabilize the processes of range contraction and isolation that have resulted in long-term population declines.

Book chapter

Conservation of greater sage-grouse- a synthesis of current trends and future management

Recent analyses of Greater Sage-Grouse (Centrocercus urophasianus) populations indicate substantial declines in many areas but relatively stable populations in other portions of the species? range. Sagebrush (Artemisia spp.) habitats neces-sary to support sage-grouse are being burned by large wildfires, invaded by nonnative plants, and developed for energy resources (gas, oil, and wind). Management on public lands, which con-tain 70% of sagebrush habitats, has changed over the last 30 years from large sagebrush control projects directed at enhancing livestock grazing to a greater emphasis on projects that often attempt to improve or restore ecological integrity. Never-theless, the mandate to manage public lands to provide traditional consumptive uses as well as recreation and wilderness values is not likely to change in the near future. Consequently, demand and use of resources contained in sagebrush land-scapes plus the associated infrastructure to sup-port increasing human populations in the western United States will continue to challenge efforts to conserve Greater Sage-Grouse. The continued widespread distribution of sage-grouse, albeit at very low densities in some areas, coupled with large areas of important sagebrush habitat that are relatively unaffected by the human footprint, sug-gest that Greater Sage-Grouse populations may be able to persist into the future. We summarize the status of sage-grouse populations and habitats, provide a synthesis of major threats and chal-lenges to conservation of sage-grouse, and suggest a roadmap to attaining conservation goals.

Book chapter

Chapter 4: A sampling and analytical approach to develop spatial distribution models for sagebrush-associated species

Understanding multi-scale floral and faunal responses to human land use is crucial for informing natural resource management and conservation planning. However, our knowledge on how land use influences sagebrush (Artemisia spp.) ecosystems is limited primarily to site-specific studies. To fill this void, studies across large regions are needed that address how species are distributed relative to type, extent, and intensity of land use. We present a study design for the Wyoming Basin Ecoregional Assessment (WBEA) to sample sagebrush-associated flora and fauna along a land cover-human land use gradient. To minimize field costs, we sampled various taxonomic groups simultaneously on transects (ungulates and lagomorphs), point counts (song birds), and area-searches of 7.29-ha survey blocks (pellet counts, burrow counts, reptile surveys, medium-sized mammals, ant mounds, rodent trapping, and vegetation sampling of native and exotic plants). We then present an exploratory approach to develop species occurrence and abundance models when a priori model building is not an option. Our study design has broad applications for large-scale evaluations of arid ecosystems.

Wyoming

Chapter 9: Occurrence of small mammals: Deer mice and challenge of trapping across large spatial extents

Small mammal communities living in sagebrush ( Artemisia spp. ) may be sensitive to habitat isolation and invasion by exotic grass species. Yet there have been no spatially explicit models to improve our understanding of landscape-scale factors determining small mammal occurrence or abundance. We live-trapped small mammals at 186 locations in the Wyoming Basin Ecoregional Assessment area to develop species distribution (habitat) models for each species. Most small mammal species (n = 14) were trapped at a only few locations. As a result, we developed a small mammal model only for the deer mouse ( Peromyscus maniculatus ). Deer mice were associated with areas having moderately productive habitat as measured by Normalized Difference Vegetation Index (NDVI), increased grassland land cover, contagion of sagebrush land cover, and proximity to intermittent water. The proportion of big sagebrush ( Artemisia tridentata ) within 0.27 km, proportion of mixed shrubland within 5 km, soil clay content, and proximity to pipelines were inversely related to the occurrence of deer mice. Understanding habitat characteristics for deer mice helps our overall understanding of the ecological processes within sagebrush habitats because deer mice act as predator, prey, competitor, and disease reservoir. Development of the empirical data necessary for spatially explicit habitat modeling of small mammal distributions at large spatial extents requires an extensive trapping effort in order to obtain enough observations to construct models, calculate robust detectability estimates, and overcome issues such as trap shyness and population cycling.

Wyoming

Chapter 10: Occurrence of non-native invasive plants: The role of anthropogenic features

The invasion of non-native plants in the Wyoming Basins Ecoregional Assessment (WBEA) area is a major economic and ecological stress, with invasions thought to be hastened by energy developments. Given the potential impacts of nonnative invasive plants and the rapid changes in land use in the WBEA, broad-scale assessments and predictive models of nonnative invasive plant distribution are needed. Using this information, the current extent of populations for targeting treatment and monitoring can be identified, the habitat affinities for forecasting where weeds may establish next determined, and the responses to individual human disturbances (such as energy developments) predicted. To address these needs, we conducted vegetation surveys across the WBEA area at 317 individual survey blocks (five plots per survey block) during the summers of 2005 and 2006. Survey blocks were stratified by both human disturbance and habitat productivity; in each of five plots per survey block the occurrence of 23 common nonnative invasive plants was recorded during early and late season surveys. Here, we report on the four most common invasive plants, crested wheatgrass ( Agropyron cristatum ), cheatgrass ( Bromus tectorum ), halogeton ( Halogeton glomeratus ), and Russian thistle ( Salsola spp. ). Occurrence models were generated for each species using random-effects logistic regression to account for nesting of plots within sample sites. Predictors of occupancy included local habitat, abiotic condition, and distance to anthropogenic features. Although occurrences of all four invasive plants were affected by habitat, abiotic, and anthropogenic factors, cheatgrass and Russian thistle were most strongly associated with anthropogenic disturbance, primarily major roads and energy well sites. We assessed relationships between environmental and anthropogenic predictors and species occurrences to identify the major factors affecting current species distribution, examined shape of the response in occurrence in relation to proximity to individual anthropogenic disturbances, and provided spatial predictions of the locations where invasive plants are most likely to occur.

Wyoming

Chapter 11: Management considerations

We conducted an ecoregional assessment of sagebrush ( Artemisia spp. ) ecosystems in the Wyoming Basins and surrounding regions (WBEA) to determine broad-scale species-environmental relationships. Our goal was to assess the potential influence from threats to the sagebrush ecosystem on associated wildlife through the use of spatially explicit occurrence and abundance models. These models were developed using information from field surveys conducted along gradients of vegetation productivity and human disturbance integrated with spatial datasets delineating land cover, topography, and human land use in the WBEA area. Our evaluation included all sagebrush-associated wildlife species across multiple taxa whose habitat requirements and distributions were appropriate for modeling and interpretation at the broad scales of this assessment. Dominant land uses were included in delineating the human footprint. Although overall levels of the cumulative human footprint were generally low across the WBEA area, oil and gas activities have decreased the amount of shrubland habitats and increased fragmentation within development regions over the last century. At the scale of this assessment, the influence of humans was primarily expressed as an indirect function through actions that altered or reduced available habitat. We identified 65 plant species of conservation concern; 28 of 40 vertebrate species associated with sagebrush were species of concern in at least one state. We modeled environmental relationships for 15 wildlife species from data collected from surveys conducted in 2005 and 2006 designed to sample multiple species and taxa along land cover and land use gradients across the WBEA area. Occurrence of 3 species was negatively influenced by human features; anthropogenic features were a positive influence for 3 species, 8 had a mixed response, and 1 had no measurable relationship. Sagebrush land cover, considered in all wildlife models, was important to most species but differed among species in the proportion of sagebrush required and at what spatial extent. For most species examined, the spatial extent at which sagebrush cover influenced the probability of occupancy was much larger than an individual’s home range size. Exotic plants were strongly associated with human features, particularly roads, which may function as linear vectors to facilitate spread of exotic plants across the WBEA area. We used coarse-grained spatial and thematic data because of the large spatial extent (350,000 km 2 ) of the WBEA area and the need for a consistent land cover map for the region. Distributions of species occurrence or abundance mapped in this assessment need to be corroborated with information on population demographics. In addition, our results should be interpreted relative to assumptions inherent in broad-scale ecoregional assessments. Our assessment provides managers with extensive and detailed maps of occurrence and abundance, allowing for status assessments of native species, diversity and richness, natural communities, and ecological systems present within the Wyoming Basins.

Wyoming