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Insights from long-term ungrazed and grazed watersheds in a salt desert Colorado Plateau ecosystem

Dryland ecosystems cover over 41% of the earth’s land surface, and living within these important ecosystems are approximately 2 billion people, a large proportion of whom are subsistence agropastoralists. Improper grazing in drylands can negatively impact ecosystem productivity, soil conservation, hydrologic processes, downstream water quantity and quality, and ultimately human health and economic well-being. Concerns regarding the degraded state of western US rangelands in the 1950s resulted in an interagency committee to study the effects of land use on runoff and erosion processes. In 1953, a federal research group established four paired watersheds in western Colorado to study the interaction of grazing by domestic livestock, runoff, and sediment yield. Exclusion of livestock from half of the watersheds dramatically reduced runoff and sediment yield after the first 10 yr—primarily due to changes in ground cover but not vegetation. Here, we report results of repeated soils and vegetation assessments of the experimental watersheds after more than 50 yr of grazing exclusion. Results show that many of the differences in soil conditions between grazed and ungrazed watersheds observed in the 1950s and 1960s were still present in 2004, despite reduced numbers of livestock: few differences in vegetation cover but large differences in biological soil crusts, soil stability, soil compaction, and soil biogeochemistry. There were differences among soil types in response to grazing history, especially soil lichen cover and soil organic matter, nitrogen, and sodium. Comparisons of ground cover measured in 2004 with those measured in 1953, 1966, and 1972 suggest much of the differences between grazed and ungrazed watersheds likely were driven by high sheep numbers during droughts in the 1950s. Persistence of these differences, despite large reductions in stocking rates , suggest the combination of overgrazing and drought may have pushed these salt desert ecosystems into a persistent, degraded ecological state.

Salt Desert Colorado Plateau Ecosystem

Fire risk in revegetated bunchgrass communities Infested with Bromus tectorum

In rangeland ecosystems, invasive annual grass replacement of native perennials is associated with higher fire risk. Large bunchgrasses are often seeded to reduce cover of annuals such as Bromus tectorum L. (cheatgrass), but there is limited information about how revegetation reduces fire risk over the long-term. For this research note, we conducted a pilot study to assess how community composition influences fire risk at 3 sites in Columbia National Wildlife Refuge in Washington, USA that were revegetated with large bunchgrasses 8 to 18 years prior to the study. At each revegetated site, five replicates with 10 plots each (plot size 10 × 10 m) were established. Fire risk was determined as the probability that a plot would completely burn following ignition at a randomly located point in each plot (i.e., if 8 of 10 plots burned fire risk was 80%). Pre-ignition, cover of bunchgrasses, cheatgrass, forbs, and surface cover characteristics were determined for each plot. Bunchgrasses successfully established to varying degrees among sites, but fire risk was still relatively high (around 73%) and did not significantly differ among sites cover. All sites had similar surface cover characteristics such as high total fuels cover (>80% at all sites) and low unvegetated gap cover (soil and soil cryptogams, <17%). Our pilot study suggests that even though revegetation may increase bunchgrass and decrease cheatgrass, fire risk remains high likely due to other surface cover characteristics. Future studies should aim to have larger variation in cover, grazing intensity, and weather conditions.

Washington

Patterns of big sagebrush plant community composition and stand structure in the western United States

Big sagebrush ( Artemisia tridentata Nutt.) plant communities are found in western North America and comprise a mix of shrubs, forbs, and grasses. Climate, topography, and soil water availability are important factors that shape big sagebrush stand structure and plant community composition; however, most studies have focused on understanding these relationships at sites in a small portion of the big sagebrush region. Our goal was to characterize detailed stand structure and plant composition patterns and identify environmental variables related to those patterns by sampling 15 sites distributed across the western United States. In each site, we characterized stand structure at the individual shrub level and at the site level. We quantified size distributions and assessed relationships among canopy volume, age, and height. We also characterized functional type cover and species composition and related those to climatic, topographic, and edaphic variables. Mean big sagebrush age ranged from 21 (± 8) to 57 (± 22) yr at individual sites, mean height ranged from 0.23 (± 0.12) to 0.67 (± 0.23) m, and mean canopy volume ranged from 0.03 (± 0.04) to 0.62 (± 0.51) m 3 . Bare ground and litter contributed the most cover (mean = 64%), followed by big sagebrush (mean = 39% of vascular plant cover). There was a negative relationship between big sagebrush cover and grass and forb cover. Species composition was related to both climate and elevation, likely because these variables influence water availability. Although our study was limited to 15 field sites, our detailed descriptions of widely distributed sites provide insight into the magnitude of variability in big sagebrush plant community structure.

Rangeland Ecology and Management

Comparison of methods to examine diet of feral horses from non-invasively collected fecal samples

Feral horses (Equus ferus caballus) have become abundant on public lands in the American West, particularly over the past 10 yr. In areas where they are overabundant, there is risk of habitat degradation. Most previous studies on diet and habitat use of feral horses were conducted more than 20 yr ago; rangelands have changed considerably in that time, so it is useful to revisit horse diets. We conducted a study to examine the diet of feral horses using noninvasive methods and subjectively compare diet analysis techniques. We collected feral horse fecal samples from a sagebrush/pinyon-juniper ecosystem in Colorado in May, August, and October 2014. We analyzed 30 fecal samples from each collection session by both microhistology and plant DNA barcoding. Both microhistology and plant DNA barcoding results indicated horse diet consisted primarily of graminoids (78.5% and 68.8%, respectively, both of which are in greater proportion than availability based on ecological site descriptions); however, the two methods differed in species composition of grasses. Similar to other studies, microhistological analyses underestimated the proportion of forbs in the diet compared with plant DNA barcoding analyses, which showed a surprisingly high contribution of forbs to the diet compared with previous studies. Our results suggest plant DNA barcoding analyses have great potential, although both methods have inherent biases.

Colorado

The influence of grazing on the spatiotemporal activity patterns of a primary sage-grouse nest predator

Perturbations in ecological processes can occur when wildlife alter their spatiotemporal activity patterns to avoid human activities that they perceive as a risk. Such perturbations can have cascading effects throughout wildlife communities. For greater sage-grouse ( Centrocercus urophasianus ; hereafter sage-grouse), nest predation plays an important role in population dynamics. Domestic cattle ( Bos taurus ) grazing has been hypothesized to increase nest predation by reducing grass height, and therefore reducing nest concealment, which may facilitate nest detection by predators. Grass height is lower on grazed pastures, but sage-grouse nest success appears similar on pastures grazed at varying intensities in several recent studies. Any reductions in nest concealment caused by grazing could potentially be offset by a localized response of one or more nest predators to the presence of cattle (i.e., the cattle avoidance hypothesis). A reduction in nest predator density or relative use within pastures could explain similar patterns of nest success on pastures grazed at varying intensities. Also, wildlife can potentially partition themselves temporally to avoid risks associated with human activities. For example, a shift in diel activity patterns by nest predators in response to cattle could result in predators being active during portions of the day when they are less efficient at locating sage-grouse nests. Thus, the effects of grazing could be offset by a temporal avoidance of cattle by predators. We deployed motion sensor cameras across six pastures to evaluate whether coyotes ( Canis latrans ; a primary sage-grouse nest predator) altered spatiotemporal activity patterns in response to cattle. We found that the probability of detecting coyotes had a positive relationship with cattle detections at camera sites (β = 0.22; 95% CI = 0.14,0.30). We also found that coyotes did not shift their diel activity patterns in response to cattle being in the pastures. Thus, in our system, similar sage-grouse nest success among pastures with different grazing intensities cannot be explained by the cattle avoidance hypothesis, at least for coyotes.

Idaho

Wildfire and postfire restoration treatments have lasting effects on rodent habitat and community composition

Rangeland fires can quickly change the structure of wildlife habitat and cause changes that persist for years to decades. To facilitate habitat recovery, postfire restoration actions often involve sowing seeds of native and nonnative perennial grasses and shrubs. Empirical information on whether such restoration activities are effective and how wildlife will respond is unknown. We evaluated the effects of wildfire and postfire seeding on rodent communities in sagebrush steppe by measuring environmental characteristics and live-trapping rodents at three wildfire locations in the northern Great Basin that burned 2–14 yr prior. Sampled plots were either 1) burned (control), 2) burned and seeded with nonnative species, 3) burned and seeded with native species, or 4) not burned (reference). Unburned reference plots had 95.7% more shrub cover and less cover of nonnative annual grasses than all burned plots. Burned plots seeded with native species had greater cover of native perennial grasses and less bare ground compared with burned plots seeded with nonnative species or control plots. Wildfire and postfire seeding significantly changed rodent community composition but not species richness. American deermouse ( Peromyscus maniculatus ) and least chipmunk ( Tamias minimus ) were less likely to occur in burned plots than in unburned reference plots. Ord’s kangaroo rat ( Dipodomys ordii ) and Piute ground squirrel ( Urocitellus mollis ) were more likely to occur in burned plots than in unburned reference plots. Sagebrush vole ( Lemmiscus curtatus ) was more likely to occur in burned plots with native seeding than with all other treatments. Species’ responses to wildfire and seeding reflected their relationships to cover of shrubs, perennial grasses, and nonnative annual grasses. These results suggest that wildfire and postfire seeding have long-lasting effects on wildlife communities. Landscape-level rodent diversity may be enhanced when small-scale disturbances or restoration actions increase landscape heterogeneity.

northern Great Basin

Long-term dynamics of production, respiration, and net CO 2 exchange in two sagebrush-steppe ecosystems

We present a synthesis of long-term measurements of CO 2 exchange in 2 US Intermountain West sagebrush-steppe ecosystems. The locations near Burns, Oregon (1995–2001), and Dubois, Idaho (1996–2001), are part of the AgriFlux Network of the Agricultural Research Service, United States Department of Agriculture. Measurements of net ecosystem CO 2 exchange ( F c ) during the growing season were continuously recorded at flux towers using the Bowen ratio-energy balance technique. Data were partitioned into gross primary productivity ( P g ) and ecosystem respiration ( R e ) using the light-response function method. Wintertime fluxes were measured during 1999/2000 and 2000/2001 and used to model fluxes in other winters. Comparison of daytime respiration derived from light-response analysis with nighttime tower measurements showed close correlation, with daytime respiration being on the average higher than nighttime respiration. Maxima of P g and R e at Burns were both 20 g CO 2 ·m −2 ·d −1 in 1998. Maxima of P g and R e at Dubois were 37 and 35 g CO 2 ·m −2 ·d −1 , respectively, in 1997. Mean annual gross primary production at Burns was 1 111 (range 475–1 715) g CO 2 ·m −2 ·y −1 or about 30% lower than that at Dubois (1 602, range 963–2 162 g CO 2 ·m −2 ·y −1 ). Across the years, both ecosystems were net sinks for atmospheric CO 2 with a mean net ecosystem CO 2 exchange of 82 g CO 2 ·m −2 ·y −1 at Burns and 253 g CO 2 ·m −2 ·y −1 at Dubois, but on a yearly basis either site could be a C sink or source, mostly depending on precipitation timing and amount. Total annual precipitation is not a good predictor of carbon sequestration across sites. Our results suggest that F c should be partitioned into P g and R e components to allow prediction of seasonal and yearly dynamics of CO 2 fluxes.

Rangeland Ecology and Management

Climate-driven interannual variability in net ecosystem exchange in the Northern Great Plains grasslands

The Northern Great Plains grasslands respond differently under various climatic conditions; however, there have been no detailed studies investigating the interannual variability in carbon exchange across the entire Northern Great Plains grassland ecosystem. We developed a piecewise regression model to integrate flux tower data with remotely sensed data and mapped the 8-d and 500-m net ecosystem exchange (NEE) for the years from 2000 to 2006. We studied the interannual variability of NEE, characterized the interannual NEE difference in climatically different years, and identified the drought impact on NEE. The results showed that NEE was highly variable in space and time across the 7 yr. Specifically, NEE was consistently low (−35 to 322 g C·m −2 ·yr −1 ) with an average annual NEE of −2 ± 242 g C·m −2 ·yr −1 and a cumulative flux of −152 g C·m −2 . The Northern Great Plains grassland was a weak source for carbon during 2000–2006 because of frequent droughts, which strongly affected the carbon balance, especially in the Western High Plains and Northwestern Great Plains. Comparison of the NEE map with a drought monitor map confirmed a substantial correlation between drought and carbon dynamics. If drought severity or frequency increases in the future, the Northern Great Plains grasslands may become an even greater carbon source.

Northern Great Plains grasslands

Using digital photography to examine grazing in montane meadows

Cattle ( Bos taurus ) numbers on national forests are allocated based on allotment grazing capacity, but spatial patterns of timing and density at smaller scales are difficult to assess. However, it is often in meadows or riparian areas that grazing may affect hydrology, biodiversity, and other important ecosystem characteristics. To explore real-time animal presence in montane meadows we distributed 18 digital cameras across nine sites in the Sierra National Forest, California. Our objectives were to document seasonal and diurnal presence of both cattle and mule deer ( Odocoileus hemionus ), identify the effects of three fencing treatments on animal distribution, and test digital photography as a tool for documenting cattle presence. We recorded 409 399 images during daylight hours for two grazing seasons, and we identified 5 084 and 24 482 cattle "marks" (instances of animal occurrence) in 2006 and 2007, respectively. Deer presence was much lower, with 331 marks in 2006 and 598 in 2007. Morning cattle presence was highest before 0800 hours both years (13.7% and 15.4% of total marks for 2006 and 2007, respectively). Marks decreased until 1100 hours and then increased around 1400 hours and remained relatively stable until 1900 hours. Marks then rose precipitously, with >20% of total marks recorded after 1900 hours both years. Deer presence was less than 10% per hour until 1800 hours, when >20% of total marks were recorded after this time both years. Among treatments, cattle marks were highest outside fences at partially fenced meadows, and deer were highest within completely fenced meadows. Our experience suggests that cameras are not viable tools for meadow monitoring due to variation captured within meadows and the time and effort involved in image processing and review.

Rangeland Ecology and Management

A common-garden study of resource-island effects on a native and an exotic, annual grass after fire

Plant-soil variation related to perennial-plant resource islands (coppices) interspersed with relatively bare interspaces is a major source of heterogeneity in desert rangelands. Our objective was to determine how native and exotic grasses vary on coppice mounds and interspaces (microsites) in unburned and burned sites and underlying factors that contribute to the variation in sagebrush-steppe rangelands of the Idaho National Lab, where interspaces typically have abiotic crusts. We asked how the exotic cheatgrass ( Bromus tectorum L.) and native bluebunch wheatgrass ( Pseudoroegneria spicata [Pursh] A. Löve) were distributed among the microsites and measured their abundances in three replicate wildfires and nearby unburned areas. We conducted a common-garden study in which soil cores from each burned microsite type were planted with seed of either species to determine microsite effects on establishment and growth of native and exotic grasses. We assessed soil physical properties in the common-garden study to determine the intrinsic properties of each microsite surface and the retention of microsite soil differences following transfer of soils to the garden, to plant growth, and to wetting/drying cycles. In the field study, only bluebunch wheatgrass density was greater on coppice mounds than interspaces, in both unburned and burned areas. In the common-garden experiment, there were microsite differences in soil physical properties, particularly in crust hardness and its relationship to moisture, but soil properties were unaffected by plant growth. Also in the experiment, both species had equal densities yet greater dry mass production on coppice-mound soils compared to interspace soils, suggesting microsite differences in growth but not establishment (likely related to crust weakening resulting from watering). Coppice-interspace patterning and specifically native-herb recovery on coppices is likely important for postfire resistance of this rangeland to cheatgrass.

Idaho

Region-wide ecological responses of arid Wyoming big sagebrush communities to fuel treatments

If arid sagebrush ecosystems lack resilience to disturbances or resistance to annual invasives, then alternative successional states dominated by annual invasives, especially cheatgrass ( Bromus tectorum L.), are likely after fuel treatments. We identified six Wyoming big sagebrush ( Artemisia tridentata ssp. wyomingensis Beetle & Young) locations (152–381 mm precipitation) that we believed had sufficient resilience and resistance for recovery. We examined impacts of woody fuel reduction (fire, mowing, the herbicide tebuthiuron, and untreated controls, all with and without the herbicide imazapic) on short-term dominance of plant groups and on important land health parameters with the use of analysis of variance (ANOVA). Fire and mowing reduced woody biomass at least 85% for 3 yr, but herbaceous fuels were reduced only by fire (72%) and only in the first year. Herbaceous fuels produced at least 36% more biomass with mowing than untreated areas during posttreatment years. Imazapic only reduced herbaceous biomass after fires (34%). Tebuthiuron never affected herbaceous biomass. Perennial tall grass cover was reduced by 59% relative to untreated controls in the first year after fire, but it recovered by the second year. Cover of all remaining herbaceous groups was not changed by woody fuel treatments. Only imazapic reduced significantly herbaceous cover. Cheatgrass cover was reduced at least 63% with imazapic for 3 yr. Imazapic reduced annual forb cover by at least 45%, and unexpectedly, perennial grass cover by 49% (combination of tall grasses and Sandberg bluegrass [ Poa secunda J. Presl.]). Fire reduced density of Sandberg bluegrass between 40% and 58%, decreased lichen and moss cover between 69% and 80%, and consequently increased bare ground between 21% and 34% and proportion of gaps among perennial plants > 2 m (at least 28% during the 3 yr). Fire, mowing, and imazapic may be effective in reducing fuels for 3 yr, but each has potentially undesirable consequences on plant communities.

Wyoming

Assessing transportation infrastructure impacts on rangelands: test of a standard rangeland assessment protocol

Linear disturbances associated with on- and off-road vehicle use on rangelands has increased dramatically throughout the world in recent decades. This increase is due to a variety of factors including increased availability of all-terrain vehicles, infrastructure development (oil, gas, renewable energy, and ex-urban), and recreational activities. In addition to the direct impacts of road development, the presence and use of roads may alter resilience of adjoining areas through indirect effects such as altered site hydrologic and eolian processes, invasive seed dispersal, and sediment transport. There are few standardized methods for assessing impacts of transportation-related land-use activities on soils and vegetation in arid and semi-arid rangelands. Interpreting Indicators of Rangeland Health (IIRH) is an internationally accepted qualitative assessment that is applied widely to rangelands. We tested the sensitivity of IIRH to impacts of roads, trails, and pipelines on adjacent lands by surveying plots at three distances from these linear disturbances. We performed tests at 16 randomly selected sites in each of three ecosystems (Northern High Plains, Colorado Plateau, and Chihuahuan Desert) for a total of 208 evaluation plots. We also evaluated the repeatability of IIRH when applied to road-related disturbance gradients. Finally, we tested extent of correlations between IIRH plot attribute departure classes and trends in a suite of quantitative indicators. Results indicated that the IIRH technique is sensitive to direct and indirect impacts of transportation activities with greater departure from reference condition near disturbances than far from disturbances. Trends in degradation of ecological processes detected with qualitative assessments were highly correlated with quantitative data. Qualitative and quantitative assessments employed in this study can be used to assess impacts of transportation features at the plot scale. Through integration with remote sensing technologies, these methods could also potentially be used to assess cumulative impacts of transportation networks at the landscape scale.

Rangeland Ecology and Management

Rangeland monitoring reveals long-term plant responses to precipitation and grazing at the landscape scale

Managers of rangeland ecosystems require methods to track the condition of natural resources over large areas and long periods of time as they confront climate change and land use intensification. We demonstrate how rangeland monitoring results can be synthesized using ecological site concepts to understand how climate, site factors, and management actions affect long-term vegetation dynamics at the landscape-scale. Forty-six years of rangeland monitoring conducted by the Bureau of Land Management (BLM) on the Colorado Plateau reveals variable responses of plant species cover to cool-season precipitation, land type (ecological site groups), and grazing intensity. Dominant C 3 perennial grasses (Achnatherum hymenoides , Hesperostipa comata) , which are essential to support wildlife and livestock on the Colorado Plateau, had responses to cool-season precipitation that were at least twice as large as the dominant C 4 perennial grass (Pleuraphis jamesii) and woody vegetation. However, these C 3 perennial grass responses to precipitation were reduced by nearly one-third on grassland ecological sites with fine- rather than coarse-textured soils, and there were no detectable C 3 perennial grass responses to precipitation on ecological sites dominated by a dense-growing shrub, Coleogyne ramosissima . Heavy grazing intensity further reduced the responses of C 3 perennial grasses to cool-season precipitation on ecological sites with coarse-textured soils and surprisingly reduced the responses of shrubs as well. By using ecological site groups to assess rangeland condition, we were able to improve our understanding of the long-term relationships between vegetation change and climate, land use, and site characteristics, which has important implications for developing landscape-scale monitoring strategies.

Arizona, Colorado, New Mexico, Utah

Vegetation sampling and management

What is the utility of vegetation measurements for wildlife managers? In the prairie, savanna, tundra, forest, steppe, and wetland regions of the world, mixtures of plant species provide wildlife with food, cover and, in some circumstances, water; the 3 essential habitat elements necessary to sustain viable wildlife populations. We define habitat in reference to use of a vegetation type by an animal (e.g., deer habitat) and vegetation type when referring to differences in vegetation stands (e.g., marsh vegetation type versus tall grass prairie vegetation type; Hall et al. 1997). In strict definition, the variety of wildlife using plants ranges from snails and voles (Microtus spp.) to bison (Bison bison) and elephants (Loxodonta spp.) in uplands and from mosquitoes and ducks to muskrats (Ondatra zibethicus) and manatees (Trichechus manatus) in wetlands. Through evolutionary processes, some wildlife species are totally dependent on vegetation for all annual life requirements, whereas other species use vegetation only for cover or food. Regardless of the role of vegetation in the sustenance of wildlife, any management or research project that requires evaluation of wildlife and vegetation type relationships on a unit of land will necessitate some form of vegetation measurement. The term vegetation can refer to a single plant or species on a specific site or a community in the landscape. Vegetation may occur naturally or be introduced, and may be live or dead. Uses of vegetation measurements are many: (1) evaluation of vegetation response to management practices, (2) estimation of carrying capacity and/or forage production, (3) characterization of cover and habitat components for an endangered species, or (4) long-term monitoring of the general trend of plant vigor or vegetation type condition. Surveying and measuring quantity and quality of vegetation within habitats are basic to wildlife research and management. Grassland, shrubland, and woodland vegetation types are comprised of populations in which individual plants are usually too numerous to inventory completely. Consequently, wildlife biologists usually use sampling techniques to make inferences about the total plant population within a given vegetation type. Vegetation sampling methodologies have evolved within several ecological disciplines (e.g., plant ecology, forestry, rangeland science) and for a variety of management or research objectives (e.g., estimating forage for ungulates, describing habitat use by passerine birds). Description of every method that has been used to sample vegetation is beyond the scope of this chapter. We describe how to measure vegetation structure, which Dansereau (1957) defined as the spatial organization (distribution) of individuals that form a stand. We have organized this chapter into a description of basic methods of vegetation sampling with examples of how those methods have been applied or modified in wildlife research and management. We assume the investigator/reader has adequate knowledge of the concepts of wildlife ecology, primary habitat requirements of wildlife species under study, and ability to systematically identify the species of wildlife and vascular plants within the geographical area of investigation.

Book chapter

Future direction of fuels management in sagebrush rangelands

Sagebrush ecosystems in the United States have been declining since EuroAmerican settlement, largely due to agricultural and urban development, invasive species, and altered fire regimes, resulting in loss of biodiversity and wildlife habitat. To combat continued conversion to undesirable ecological states and loss of habitat to invasive species fueled by frequent fire, a variety of fuel treatments, including networks of fuel breaks, are being implemented or proposed in sagebrush ecosystems, particularly in and around the Great Basin. In this forum paper we briefly review current knowledge of common fuel treatment approaches, their intended benefits, potential risks, and limitations. We additionally discuss challenges for fuel treatment strategies in the context of changes in climate, invasive species, wildlife habitat, and human population, and we explore how advances in geospatial technologies, monitoring, and fire behavior modeling, as well as accounting for social context, can improve the efficacy of fuels management in sagebrush ecosystems. Finally, given continued potential for ecosystem transformation, we describe approaches to future fuels management by considering the applicability of the Resist-Accept-Direct (RAD) framework. The intent of the paper is to provide scientists and land managers with key information and a forward-thinking framework for fuels science and adaptive management that can respond to both expected and unexpected changes in sagebrush rangelands.

Rangeland Ecology and Management

Remote camera-trap methods and analyses reveal impacts of rangeland management on Namibian carnivore communities

Assessing the abundance and distribution of mammalian carnivores is vital for understanding their ecology and providing for their long-term conservation. Because of the difficulty of trapping and handling carnivores many studies have relied on abundance indices that may not accurately reflect real abundance and distribution patterns. We developed statistical analyses that detect spatial correlation in visitation data from combined scent station and camera-trap surveys, and we illustrate how to use such data to make inferences about changes in carnivore assemblages. As a case study we compared the carnivore communities of adjacent communal and freehold rangelands in central Namibia. We used an index of overdispersion to test for repeat visits to individual camera-trap scent stations and a bootstrap simulation to test for correlations in visits to camera neighbourhoods. After distilling our presence-absence data to the most defensible spatial scale, we assessed overall carnivore visitation using logistic regression. Our analyses confirmed the expected pattern of a depauparate fauna on the communal rangelands compared to the freehold rangelands. Additionally, the species that were not detected on communal sites were the larger-bodied carnivores. By modelling these rare visits as a Poisson process we illustrate a method of inferring whether or not such patterns are because of local extinction of species or are simply a result of low sample effort. Our Namibian case study indicates that these field methods and analyses can detect meaningful differences in the carnivore communities brought about by anthropogenic influences. ?? 2007 FFI.

Oryx

Assessing rangelands

It is important for land managers and technical assistance specialists to be able to assess the health of rangelands in order to know where to focus management efforts. The complexity of ecological processes, and the inherent expense of directly measuring site integrity, suggests a need for an evaluation process that focuses instead on biological and physical attributes. In a collaborative effort, the USGS, ARS, BLM, and NRCS have jointly developed a system in which 17 indicators are used to gauge three attributes of rangeland health. A qualitative, observational procedure provides an assessment of the functional status of these indicators. This quick assessment technique, by providing an understanding about each attribute, helps interpret rangeland health.

Fact Sheet

Ecological thresholds as a basis for defining management triggers for National Park Service vital signs: case studies for dryland ecosystems

Threshold concepts are used in research and management of ecological systems to describe and interpret abrupt and persistent reorganization of ecosystem properties (Walker and Meyers, 2004; Groffman and others, 2006). Abrupt change, referred to as a threshold crossing, and the progression of reorganization can be triggered by one or more interactive disturbances such as land-use activities and climatic events (Paine and others, 1998). Threshold crossings occur when feedback mechanisms that typically absorb forces of change are replaced with those that promote development of alternative equilibria or states (Suding and others, 2004; Walker and Meyers, 2004; Briske and others, 2008). The alternative states that emerge from a threshold crossing vary and often exhibit reduced ecological integrity and value in terms of management goals relative to the original or reference system. Alternative stable states with some limited residual properties of the original system may develop along the progression after a crossing; an eventual outcome may be the complete loss of pre-threshold properties of the original ecosystem. Reverting to the more desirable reference state through ecological restoration becomes increasingly difficult and expensive along the progression gradient and may eventually become impossible. Ecological threshold concepts have been applied as a heuristic framework and to aid in the management of rangelands (Bestelmeyer, 2006; Briske and others, 2006, 2008), aquatic (Scheffer and others, 1993; Rapport and Whitford 1999), riparian (Stringham and others, 2001; Scott and others, 2005), and forested ecosystems (Allen and others, 2002; Digiovinazzo and others, 2010). These concepts are also topical in ecological restoration (Hobbs and Norton 1996; Whisenant 1999; Suding and others, 2004; King and Hobbs, 2006) and ecosystem sustainability (Herrick, 2000; Chapin and others, 1996; Davenport and others, 1998). Achieving conservation management goals requires the protection of resources within the range of desired conditions (Cook and others, 2010). The goal of conservation management for natural resources in the U.S. National Park System is to maintain native species and habitat unimpaired for the enjoyment of future generations. Achieving this goal requires, in part, early detection of system change and timely implementation of remediation. The recent National Park Service Inventory and Monitoring program (NPS I&M) was established to provide early warning of declining ecosystem conditions relative to a desired native or reference system (Fancy and others, 2009). To be an effective tool for resource protection, monitoring must be designed to alert managers of impending thresholds so that preventive actions can be taken. This requires an understanding of the ecosystem attributes and processes associated with threshold-type behavior; how these attributes and processes become degraded; and how risks of degradation vary among ecosystems and in relation to environmental factors such as soil properties, climatic conditions, and exposure to stressors. In general, the utility of the threshold concept for long-term monitoring depends on the ability of scientists and managers to detect, predict, and prevent the occurrence of threshold crossings associated with persistent, undesirable shifts among ecosystem states (Briske and others, 2006). Because of the scientific challenges associated with understanding these factors, the application of threshold concepts to monitoring designs has been very limited to date (Groffman and others, 2006). As a case in point, the monitoring efforts across the 32 NPS I&M networks were largely designed with the knowledge that they would not be used to their full potential until the development of a systematic method for understanding threshold dynamics and methods for estimating key attributes of threshold crossings. This report describes and demonstrates a generalized approach that we implemented to formalize understanding and estimating of threshold dynamics for terrestrial dryland ecosystems in national parks of the Colorado Plateau. We provide a structured approach to identify and describe degradation processes associated with threshold behavior and to estimate indicator levels that characterize the point at which a threshold crossing has occurred or is imminent (tipping points) or points where investigative or preventive management action should be triggered (assessment points). We illustrate this method for several case studies in national parks included in the Northern and Southern Colorado Plateau NPS I&M networks, where historical livestock grazing, climatic change, and invasive species are key agents of change. The approaches developed in these case studies are intended to enhance the design, effectiveness, and management-relevance of monitoring efforts in support of conservation management in dryland systems. They specifically enhance National Park Service (NPS) capacity for protecting park resources on the Colorado Plateau but have applicability to monitoring and conservation management of dryland ecosystems worldwide.

Colorado Plateau