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A strategic and science-based framework for management of invasive annual grasses in the sagebrush biome

In the last 20 years, the North American sagebrush biome has lost over 500,000 ha of intact and largely intact sagebrush plant communities on an annual basis. Much of this loss has been associated with expansion and infilling of invasive annual grasses (IAGs). These species are highly competitive against native perennial grasses in disturbed environments, and create fuel conditions that increase both the likelihood of fire ignition and the ease of wildfire spread across large landscapes. Given the current rate of IAG expansion in both burned and unburned rangelands, ameliorating the IAG threat will involve a range-wide paradigm shift from opportunistic and reactive management, to a framework that spatially prioritizes maintenance of largely intact, uninvaded areas and improvement of invaded habitats in strategic locations. We created a framework accompanied by biome-wide priority maps using geospatial overlays that target areas to MAINTAIN large, uninvaded areas as natural resource anchors through activities to prevent IAGs and IMPROVE areas to reduce invasions with the highest potential for management efforts to succeed in restoring large, intact landscapes. We then offer three case studies to illustrate the use of these concepts and map products at multiple scales. Our map products operate at the biome scale using regional data sources but additional data sources may be needed to inform local conservation planning. However, the basic strategic management principles of a) maintaining the intact and uninvaded areas that we can least afford to lose to IAGs and b) improving areas where we have a higher likelihood of restoration success, is timely, relevant, and scalable from the biome to local levels.

Rangeland Ecology & Management↗

Transient population dynamics: Relations to life history and initial population state

Most environments are variable and disturbances (e.g., hurricanes, fires) can lead to substantial changes in a population's state (i.e., age, stage, or size distribution). In these situations, the long-term (i.e., asymptotic) measure of population growth rate (??1) may inaccurately represent population growth in the short-term. Thus, we calculated the short-term (i.e., transient) population growth rate and its sensitivity to changes in the life-cycle parameters for three bird and three mammal species with widely varying life histories. Further, we performed these calculations for initial population states that spanned the entire range of possibilities. Variation in a population's initial net reproductive value largely explained the variation in transient growth rates and their sensitivities to changes in life-cycle parameters (all AICc ??? 6.67 units better than the null model, all R2 ??? 0.55). Additionally, the transient fertility and adult survival sensitivities tended to increase with the initial net reproductive value of the population, whereas the sub-adult survival sensitivity decreased. Transient population dynamics of long-lived, slow reproducing species were more variable and more different than asymptotic dynamics than they were for short-lived, fast reproducing species. Because ??1 can be a biased estimate of the actual growth rate in the short-term (e.g., 19% difference), conservation and wildlife biologists should consider transient dynamics when developing management plans that could affect a population's state, or whenever population state could be unstable.

Ecological Modelling↗

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↗

What determines the effectiveness of Pinyon-Juniper clearing treatments? Evidence from the remote sensing archive and counter-factual scenarios

In the intermountain western US, expansion of Pinyon ( Pinus edulis) and Juniper ( Juniperus spp. ) woodlands (PJ) into grasslands and shrublands is a pervasive phenomenon, and an example of the global trend towards enhanced woody growth in drylands. Due to the perceived impacts of these expansions on ecosystem services related to biodiversity, hydrology, soil stability, fire prevention, and livestock forage, mechanical and chemical PJ reduction treatments have been a long-standing practice in the region. More recently, PJ reduction practices have come under enhanced public scrutiny, due to potential impacts on PJ-dependent wildlife, risk of erosion due to soil disturbance, and cost effectiveness due to variable rates of long-term success. Moreover, there is growing interest in understanding the biotic, abiotic, and management conditions under which PJ reduction treatments are effective. Here, we evaluated PJ reduction treatment outcomes leveraging large, curated databases of land treatments, new remotely sensed fractional cover time-series products, gridded climate and soils data, and analytical approaches adopted from the econometric literature. From 302 treatment events and 1569 distinct treatment polygons we found evidence that treatments reduced tree cover and largely increased shrub and perennial herbaceous cover for 10 or more years. However, treatments were also associated with increases in annual, likely non-native, herbaceous cover . Importantly, we noted treatment outcomes varied by landscape context, with some soil and geomorphic settings exhibiting consistent returns to pre-treatment conditions within 10–15 years, and others exhibiting more persistent changes in functional type composition. Despite the overall trends we observed, there was considerable unexplained variability in outcomes from treatment to treatment, highlighting the need for caution and attention to local geomorphic and biological context in planning future treatments.

Arizona, Colorado, New Mexico, Utah↗

Invasive buffelgrass detection using high-resolution satellite and UAV imagery on Google Earth Engine

Methods to detect and monitor the spread of invasive grasses are critical to avoid ecosystem transformations and large economic costs. The rapid spread of non‐native buffelgrass (Pennisetum ciliare) has intensified fire risk and is replacing fire intolerant native vegetation in the Sonoran Desert of the southwestern US. Coarse‐resolution satellite imagery has had limited success in detecting small patches of buffelgrass, whereas ground‐based and aerial survey methods are often cost prohibitive. To improve detection, we trained 2 m resolution DigitalGlobe WorldView‐2 satellite imagery with 12 cm resolution unmanned aerial vehicle (UAV) imagery and classified buffelgrass on Google Earth Engine, a cloud computing platform, using Random Forest (RF) models in Saguaro National Park, Arizona, USA. Our classification models had an average overall accuracy of 93% and producer's accuracies of 94–96% for buffelgrass, although user's accuracies were low. We detected a 2.92 km 2 area of buffelgrass in the eastern Rincon Mountain District (1.07% of the total area) and a 0.46 km 2 area (0.46% of the total area) in the western Tucson Mountain District of Saguaro National Park. Buffelgrass cover was significantly greater in the Sonoran Paloverde‐Mixed Cacti Desert Scrub vegetation type, on poorly developed Entisols and Inceptisol soils and on south‐facing topographic aspects compared to other areas. Our results demonstrate that high‐resolution imagery improve on previous attempts to detect and classify buffelgrass and indicate potential areas where the invasive grass might spread. The methods demonstrated in this study could be employed by land managers as a low‐cost strategy to identify priority areas for control efforts and continued monitoring.

Arizona↗

Biocrust and seed placement influence emergence rates of perennial grass Elymus elymoides across five North American deserts

1. Dryland vascular plant emergence is often limited by water availability especially with projected climate and precipitation changes. Biological soil crusts (biocrusts) can promote water retention and nutrient availability that benefit germination, and emergence yet can also act as a surface barrier preventing critical seed soil contact and hindering emergence. Alongside these factors, dryland fire frequency has increased with the inclusion of invasive species and vegetation structural changes. With enhanced continuous fine fuel distribution there is a high potential to disrupt biocrust-plant interactions and influence associated management actions. 2. This study explores the dynamic relationship between biocrusts and fire-related heating effects on seedling emergence across five North American deserts: the Chihuahuan Desert, Colorado Plateau, Great Basin, Mojave Desert and Sonoran Desert. We conducted a greenhouse-based seedling emergence experiment using Elymus elymoides (bottlebrush squirreltail), a common perennial grass, with biocrust and bare soil mesocosms in which half were heated to mimic the effects of wildfire temperature. 3. The variables that had the greatest influence on germination rate and germination timing were the presence of biocrust and seed placement (on top of vs within the biocrust/soil matrix). Emergence rate was greatest atop bare soil followed by seeds inserted into biocrust. Emergence timing was faster with biocrust present, but only when seeds were inserted into it. Desert origin of biocrust and soil collection also influenced germination where the probability of any one seed emerging was highest in the Chihuahuan and Mojave desert sites relative to the Sonoran desert site which showed the lowest probability. Heating had mixed effects whereby it increased the likelihood of emergence but did not affect the overall rate or timing. 4. Synthesis and applications . This study underscores the importance of healthy and impaired biocrusts in dryland systems and suggests ways in which the combination of biocrust and seed placement can influence plant establishment, in addition to providing insight into seeding strategies for managers and restoration practitioners working in dryland sites.

Arizona, California, Colorado, Nevada, New Mexico↗

Deer do not affect short-term rates of vegetation recovery in overwash fans on Fire Island after Hurricane Sandy

1. Coastal resilience is threatened as storm-induced disturbances become more frequent and intense with anticipated changes in weather patterns. After severe storms, rapid recovery of vegetation, especially that of dune-stabilizing plants, is a fundamental property of coastal resilience. Herbivores may affect resilience by selectively foraging palatable plant species in disturbed areas. Knowledge of herbivore impacts to dune recovery after storm events is crucial to management of coastal properties. 2. We combined imagery classification, wildlife monitoring, and trend analysis to investigate effects of white-tailed deer on recovery rates of vegetation over four years post-storm in nine areas overwashed. We estimated local deer density with trail cameras, coupled deer density with primary productivity, and assessed the relationship between deer density and rates of vegetation recovery in overwash fans. 3. Pre-storm vegetation cover consisted of shrubs and sporadic patches of beachgrass. Post-storm cover was dominated by beachgrass. At current recovery rates, vegetation coverage will return to pre-storm conditions within the decade, though community transition from grasses to shrubs will take longer and will vary by site with the rate of dune formation. 4. The effect of deer on rates of vegetation recovery was negative, but not statistically significant nor biologically compelling. Although effects of trampling are evident in classified imagery, deer foraging on beachgrass had little effect on rates of spread throughout overwash fans. 5. Our research provides perhaps the first assessment of the effects of deer on post-storm vegetation recovery. While the rate of spread of the primary dune-building plant species was not deleteriously affected by deer, locally high deer densities will likely affect the establishment and development of more palatable herbs and shrubs.

New York↗

Appropriate sample sizes for monitoring burned pastures in sagebrush steppe: How many plots are enough, and can one size fit all?

Statistically defensible information on vegetation conditions is needed to guide rangeland management decisions following disturbances such as wildfire, often for heterogeneous pastures. Here we evaluate the number of plots needed to make informed adaptive management decisions using >2000 plots sampled on the 2015 Soda Fire that burned across 75 pastures and 113,000 ha in Idaho and Oregon, USA. We predicted that the number of plots required to generate a threshold of standard error/mean ≤0.2 (TSR, threshold sampling requirement) for plant cover within pasture units would vary between sampling methods (rapid ocular versus grid-point intercept) and among plot sizes (1, 6, or 531 m2), as well as relative to topography, elevation, pasture size, complexity of soils and vegetation treatments applied, and dominance by exotic annual or perennial grasses. Sampling was adequate for determining exotic annual and perennial grass cover in about half of the pastures. A tradeoff in number versus size of plots sampled was apparent, whereby TSR was attainable with less area searched using smaller plot sizes (1 compared to 531 m2) in spite of less variability between larger plots. TSR for both grass types decreased as their dominance increased (0.5-1.5 plots per % cover increment). TSR decreased for perennial grass but increased for exotic annual grass with higher elevations. TSR increased with standard deviation of elevation for perennial grass sampled with grid-point intercept. Sampling effort could be more reliably predicted from landscape variables for the grid-point compared to ocular sampling method. These findings suggest that adjusting the number and size of sample plots within a pasture or burn area using easily determined landscape variables could increase monitoring efficiency and effectiveness.

Rangeland Ecology and Management↗

Patchy response of cheatgrass and nontarget vegetation to indaziflam and imazapic applied after wildfire in sagebrush steppe

Control of nonnative grasses is needed where they are altering fire regimes and degrading rangelands, such as cheatgrass ( Bromus tectorum ) invasion of perennial sagebrush-steppe communities. Aerial broadcast of the pre-emergent and postemergent herbicide imazapic has been used for decades over vast areas to control cheatgrass after fire. Recent small-scale studies indicate that the pre-emergent herbicide indaziflam may provide more enduring cheatgrass control. We evaluated landscape-level vegetation responses to indaziflam sprayed in replicated areas at 66.7 g · ai · ha −1 , with and without imazapic (66.1 g · ai · ha −1 ) over almost 500 ha of sagebrush steppe. Herbicides were strip-sprayed by helicopter in the fall of 2019 in subregions that either 1) had burned in the summer of 2019 and had moderate background cheatgrass invasion, 2) had burned in 2011 and became heavily invaded, or 3) were burned in both 2011 and 2019 and had intermediate invasion. Tarps were temporarily deployed to intercept herbicides and create untreated controls. Overall, indaziflam + imazapic had greater initial control of cheatgrass, but by 2023, both treatments led to similar ∼17 percentage-point reductions in cheatgrass cover. Cheatgrass individuals that “escaped” the herbicide treatment grew exceptionally large and fecund. There were no reductions in cover in any native vegetation type, including biocrusts, and nontarget increases in cover were observed for 1) deep-rooted perennial grasses treated with indaziflam + imazapic in the 2011 burn subregion and 2) the shallow-rooted Sandberg bluegrass ( Poa secunda ) treated with either herbicide in the 2011 or 2011 + 2019 burn subregions. Consideration of burn legacies, pretreatment landscape condition, and evenness of treatment application may improve restoration outcomes and help prioritize management allocation, timing, and treatment expectations.

Idaho↗

Landscape-scale forest restoration decreases vulnerability to drought mortality under climate change in southwest USA ponderosa forest

Drought-induced tree mortality is predicted to increase in dry forests across the western USA as future projections show hotter, drier climates potentially resulting in large-scale tree die-offs, changes in species composition, and loss of forest ecosystem services, including carbon storage. While some studies have found that forest stands with greater basal areas (BA) have higher drought mortality, many have not evaluated the extent to which forest structure, either overly dense forests due to fire suppression or forests restored to lower densities, interacts with drought mortality. The southwestern USA is particularly susceptible to tree mortality due to the predicted increases in temperature, drier soils, and forests with high density. Our objective was to evaluate how ponderosa pine mortality is expected to be influenced by the Four Forests Restoration Initiative, a large-scale forest restoration effort ongoing in northern Arizona, USA, that will reduce stand BA by approximately 40%. Specifically, we modeled drought mortality in three time periods, one contemporary (1970-2010), and two future (2020-2059 and 2060-2099) under three restoration scenarios: no thinning, 4FRI thinning, and a BA reduction beyond the 4FRI plan (4FRI-intensive). We estimated mortality using 11 climate models under two emissions scenarios. Without thinning, our model predicted that by mid-century (2020-2059), changes in climate could increase annual ponderosa pine mortality rates by 45-57% over contemporary rates. However, with thinning, mid-century mortality was predicted to remain near or below contemporary rates and these rates are 31-35% (4FRI) and 46-51% (4FRI-intensive) less than the mid-century scenarios without thinning. Our study shows that while climate change is likely to increase tree mortality rates, large-scale forest restoration projects, such as 4FRI, have the potential to ameliorate the effects of climate change and keep mortality rates near contemporary levels for decades.

Arizona↗

Africa’s drylands in a changing world: Challenges for wildlife conservation under climate and land-use changes in the Greater Etosha Landscape

Proclaimed in 1907, Etosha National Park in northern Namibia is an iconic dryland system with a rich history of wildlife conservation and research. A recent research symposium on wildlife conservation in the Greater Etosha Landscape (GEL) highlighted increased concern of how intensification of global change will affect wildlife conservation based on participant responses to a questionnaire. The GEL includes Etosha and surrounding areas, the latter divided by a veterinary fence into large, private farms to the south and communal areas of residential and farming land to the north. Here, we leverage our knowledge of this ecosystem to provide insight into the broader challenges facing wildlife conservation in this vulnerable dryland environment. We first look backward, summarizing the history of wildlife conservation and research trends in the GEL based on a literature review, providing a broad-scale understanding of the socioecological processes that drive dryland system dynamics. We then look forward, focusing on eight key areas of challenge and opportunity for this ecosystem: climate change, water availability and quality, vegetation and fire management, adaptability of wildlife populations, disease risk, human-wildlife conflict, wildlife crime, and human dimensions of wildlife conservation. Using this model system, we summarize key lessons and identify critical threats highlighting future research needs to support wildlife management. Research in the GEL has followed a trajectory seen elsewhere reflecting an increase in complexity and integration across biological scales over time. Yet, despite these trends, a gap exists between the scope of recent research efforts and the needs of wildlife conservation to adapt to climate and land-use changes. Given the complex nature of climate change, in addition to locally existing system stressors, a framework of forward-thinking adaptive management to address these challenges, supported by integrative and multidisciplinary research could be beneficial. One critical area for growth is to better integrate research and wildlife management across land-use types. Such efforts have the potential to support wildlife conservation efforts and human development goals, while building resilience against the impacts of climate change. While our conclusions reflect the specifics of the GEL ecosystem, they have direct relevance for other African dryland systems impacted by global change.

Africa, Greater Etosha Landscape↗

The potential influence of changing climate on the persistence of salmonids of the inland west

The Earth's climate warmed steadily during the 20th century, and mean annual air temperatures are estimated to have increased by 0.6°C (Intergovernmental Panel on Climate Change, 2007). Although many cycles of warming and cooling have occurred in the past, the most recent warming period is unique in its rate and magnitude of change (Siegenthaler and others, 2005) and in its association with anthropogenic emissions of greenhouse gases (Intergovernmental Panel on Climate Change , 2007). The climate in the western United States warmed in concert with the global trend but at an accelerated rate (+0.8°C during the 20th century; Saunders and others, 2008). The region could also prove especially sensitive to future changes because the relatively small human population is growing rapidly, as are demands on limited water supplies. Regional hydrological patterns are dominated by seasonal snow accumulation at upper elevations. Most of the region is relatively dry, and both terrestrial and aquatic ecosystems are strongly constrained b y water availability (Barnett and others, 2008; Brown and others, 2008). Stream environments are dynamic and climatically extreme, and salmonid fishes are the dominant elements of the native biodiversity (McPhail and Lindsey, 1986; Waples and others, 2008). Salmonids have broad economic and ecologic importance, but a century of intensive water resource development, nonnative fish stocking, and land use has significantly reduced many populations and several taxa are now protected under the Endangered Species Act (Thurow and others, 1997; Trotter, 2008). Because salmonids require relatively pristine, cold water environments and are often isolated in headwater habitats, members of this group may be especially vulnerable to the effects of a warming climate (Keleher and Rahel, 1996; Rieman and others, 2007; Williams and others, 2009). Warming during the 20th century drove a series of environmental trends that have profound implications for many aspects of salmonid habitat, including disturbance regimes such as wildfire, and unfavorable changes to thermal and hydrologic properties of aquatic systems. Warmer air temperatures have been associated with decreased winter snow accumulations, have accelerated snowmelt, and have advanced the timing of peak runoff by several days to weeks across most of western North America (Stewart and others, 2005; Barnett and others, 2008). Less snow and earlier runoff decrease aquifer recharge, make less water available for groundwater inputs to streams, and are contributing to widespread decreases in summer low flows (Stewart and others, 2005; Rood and others, 2008; Luce and Holden 2009). Interannual variability in stream flow is increasing, as is the persistence of multi-year extreme conditions (McCabe and others, 2004; Pagano and Garen 2005). In many areas of western North America, flood risks have increased in association with warmer temperatures during the 20th century (Hamlet and Lettenmaier, 2005). Streams where midwinter temperatures are near freezing have proven especially sensitive to increased flooding because of associated transitional hydrological patterns (mixtures of rainfall and snowmelt) and propensity for occasional rain-on-snow events to rapidly melt winter snowpack and generate large floods (Hamlet and Lettenmaier, 2005). Stream temperatures in many areas are increasing (Peterson and Kitchell, 2001; Morrison and others, 2002; Bartholow, 2005; Kaushal and others, 2010), due to both air temperature increases and reduced summer flows that make streams more sensitive to warmer air temperatures (Isaak and others, 2010). In recent decades, wildfires have become more common across much of the western United States during periods of more frequent droughts (Westerling and others, 2006; Hoerling and Eischeid, 2007), and local stream temperature can increase in postfire environments (Gresswell, 1999; Dunham and others, 2007). Fire-related temperature increase within streams is commonly a transient phenomenon, lasting only until riparian vegetation has recovered (Gresswell, 1999); however, ongoing climate change could preclude recovery to higher stature, prefire vegetation types in some areas (McKenzie and others, 2004; van Mantgem and Stephenson, 2007), resulting in a loss of critical riparian shading. Additionally, when wildfires occur in steep mountain topographies, the vegetation that stabilize s soils on hillslopes is often killed and landslides become more prevalent (Gresswell, 1999). Landslides int o stream channels form debris flows composed of sediment slurries and dead trees that can scour channels to bedrock and further exacerbate stream heating, delay recovery of riparian areas, or extirpate fish populations (Gresswell, 1999; May and Gresswell, 2003; Dunham and others, 2007). Changes in stream environments will shift habitat distributions, sometimes unpredictably, in both time and space for many salmonid fishes. Water temperature fundamentally influences aquatic ecosystem health because distribution, reproduction, fitness, and survival of ectothermic organisms are inextricably linked to the thermal regime of the environment. Historically, research has focused on defining lethal thermal limits of salmonids (Eaton and others, 1995; Selong and others, 2001; Todd and others, 2008); however, water temperature is known to be important in biological processes at a variety of spatial scales and levels of biological organization (Rahel and Olden, 2008; McCullough and others, 2009). For instance, trout are affected directly by water temperature through feeding, metabolism, and growth rates, and indirectly by factors such as prey availability and species interactions (Wehrly and others, 2007; Rahel and Olden, 2008). Where cold water temperatures currently limit habitat suitability and distributions of some species (for example, at the highest and most northerly distributional extents; Nakano and others, 1996; Coleman and Fausch, 2007), a warming climate may gradually increase the quality and extent of suitable habitat. Over time, previously constrained populations are expected to expand into these new habitats and increase in number. Some evidence suggests this may already be happening in Alaska, where streams in recently deglaciated areas are being colonized by emigrants from nearby salmon and char populations (Milner and others, 2000). Unfortunately, many of the sensitive salmonid species that are often the focus of western managers are unlikely to benefit from future water temperature increases. Warmer stream temperatures will facilitate invasion by nonnative species that are broadly established in downstream areas into upstream areas where they will compete with native species (Rieman and others, 2006; Rahel and Olden, 2008; Fausch and others, 2009). In other cases, warmer stream temperatures will render thermally suitable habitats unsuitable in downstream areas and effect net losses of habitat because upstream distributions are often constrained by streams that are too small or steep (Hari and others, 2006; Isaak and others, 2010). Both scenarios are realistic for fish species like bull trout ( Salvelinus confluentus ) (Rieman and others, 2006; Rieman and others, 2007), the various subspecies of cutthroat trout ( Oncorhynchus clarkii ) (Williams and others, 2009), Gila trout ( Oncorhynchus gilae gilae ) (Kennedy and others, 2008), and Apache trout ( Oncorhynchus gilae apache ) (Rinne and Minckley, 1985; Carmichael and others, 1993). As native species are increasingly confined to smaller and more isolated habitats by a gradually warming climate, the effects of wildfires (whether related to lethal changes in water quality during a fire, channel debris flows, or chronic postfire warming ) could have greater proportional effects on remaining habitats (for example, Brown and others, 2001; Rieman and others, 2007). If these changes were accompanied by additional hydrologic alterations associated with changes to the magnitude, frequency, duration, timing, and rate of change of discharge patterns (Jager and others, 1999; Henderson and others, 2000), populations may begin to lose some of their historic resilience and become ever more susceptible to local extirpations. As dramatic and extensive as climatic and environmental trends are for salmonid habitats, global climate models (GCMs) project that many of these trends will continue and even accelerate until at least the middle of the 21st century (Intergovernmental Panel on Climate Change, 2007). Current projections suggest mean annual air temperatures will increase by an additional 1–3°C, and early indications are that climate trajectory is at the higher end of this range (Pittock, 2006; Raupach and others, 2007). Although predicted changes vary considerably, even the most conservative estimates suggest a warming rate that will be twice that observed during the 20th century. Projections for the midcentury are most certainly due to the effects of greenhouse gases already emitted or predicted in the short term, uncertainties of the effects of longer-term greenhouse gas emissions, short-term climate cycles, and process errors associated with climate models (Cox and Stephenson, 2007). Projections of changes in total precipitation are less certain than those for air temperatures, but most GCMs project relatively small changes in the Northwest, with the exception of slightly drier summer periods (Mote and others, 2008; Karl and others, 2009). In the Southwest, however, significant decreases (such as 15–30 percent ) are projected during most periods of the year, and this area is one of the few for which Intergovernmental Panel on Climate Change (2007) precipitation projections have a high level of certainty (Hoerling and Eischeid, 2007; Karl and others, 2009). Clearly, managers of native salmonids in the wester n United States should consider adjusting management strategies to accommodate a warmer and possibly drier future (Williams and others, 2009). Tools are needed to forecast where important changes may occur and how conservation efforts should be prioritized. In this Open-File Report, we document our initial efforts in this regard for 10 species and subspecies of inland trout and Montana Arctic grayling ( Thymallus arcticus ) across the western United States.

Arizona, California, Colorado, Idaho, Montana, Nev↗

Prescribed fire and other fuel-reduction treatments alter ground spider assemblages in a Southern Appalachian hardwood forest

Prescribed burns and understory thinnings are forest management practices aimed at reducing fuel loads to lessen wildfire threat in the Southern Appalachians, USA. Spiders play a critical role in forest ecosystems by controlling insect populations and providing an important food source for vertebrates. We used pitfall and colored pan traps to investigate how abundance, species richness, and diversity of spiders differed among three fuel reduction treatments administered repeatedly over a 15-year period and untreated controls. Additionally, we examined how spiders responded to one round (before and after) of fuel reduction treatments. We established treatments within the 15-year period as follows: mechanical understory removal (twice; M), prescribed burning (four times; B), mechanical understory removal followed one year later by high-severity prescribed burns and three subsequent burns (MB), and untreated controls (C). Our study period (2014–2016) occurred after multiple prescribed burns and two rounds of mechanical understory removal had occurred. Salticidae and Lycosidae were the two most commonly collected spider families in Southern Appalachian hardwood forests. Generally, we found increased spider abundances within all fuel-reduction treatments compared to controls. Individual spider families and species showed variable responses to treatments, but abundance of several spider families was greater in one or more fuel-reduction treatments than in controls. Additionally, abundance of several spider families and hunting/web building guilds (webs built for hunting purposes or defense) exhibited yearly differences to the last round of fuel-reduction treatments. Overall, our results suggest that changes in the overstory and understory of a forest are important drivers of regional spider abundance and assemblages, and forest management practices that modify forest structure can dramatically alter spider abundance and richness, usually in a positive manner.

North Carolina↗

Influence of management and precipitation on carbon fluxes in greatplains grasslands

Suitable management and sufficient precipitation on grasslands can provide carbon sinks. The net carbon accumulation of a site from the atmosphere, modeled as the Net Ecosystem Productivity (NEP), is a useful means to gauge carbon balance. Previous research has developed methods to integrate flux tower data with satellite biophysical datasets to estimate NEP across large regions. A related method uses the Ecosystem Performance Anomaly (EPA) as a satellite-derived indicator of disturbance intensity (e.g., livestock stocking rate, fire, and insect damage). To better understand the interactions among management, climate, and carbon dynamics, we evaluated the relationship between EPA and NEP data at the 250 m scale for grasslands in the Central Great Plains, USA (ranging from semi-arid to mesic). We also used weekly estimates of NEP to evaluate the phenology of carbon dynamics, classified by EPA (i.e., by level of disturbance impact). Results show that the cumulative carbon balance over these grasslands from 2000 to 2008 was a weak net sink of 13.7 g C m −2 yr −1 . Overall, NEP increased with precipitation (R 2 = 0.39, P < 0.05) from west to east. Disturbance influenced NEP phenology; however, climate and biophysical conditions were usually more important. The NEP response to disturbance varies by ecoregion, and more generally by grassland type, where the shortgrass prairie NEP is most sensitive to disturbance, the mixed-grass prairie displays a moderate response, and tallgrass prairie is the least impacted by disturbance (as measured by EPA). Sustainable management practices in the tallgrass and mixed-grass prairie may potentially induce a period of average net carbon sink until a new equilibrium soil organic carbon is achieved. In the shortgrass prairie, management should be considered sustainable if carbon stocks are simply maintained. The consideration of site carbon balance adds to the already difficult task of managing grasslands appropriately to site conditions. Results clarify the seasonal and interannual dynamics of NEP, specifically the influence of disturbance and moisture availability.

Ecological Indicators↗

Mid-contract management alters conservation reserve program vegetation in the central and western United States

Disturbances such as grazing, fire, and burrowing are historically important in North American grasslands, and plans for restoring disturbance regimes are often required for successful restoration. The U.S. Department of Agriculture’s Conservation Reserve Program (CRP) has become the dominant grassland restoration mechanism in many areas, and requires planned disturbances known as mid-contract management (MCM). We recorded evidence of MCM in CRP fields across a 14-state region of the western and central United States, then revisited fields after one to five years to characterize bare ground and vegetative cover and composition using edge-of-road visual surveys. We found a reduced cover of grasses up to five years after MCM, and a concomitant increased cover of flowering forbs and diversity of pollinator-friendly forbs. There was little measurable change in overall plant cover or bare ground cover between one and five years after MCM, though bare soil cover did increase slightly. Baseline tree and shrub covers were very low on average but highly variable due to outliers with high woody cover. After MCM, the presence of woody vegetation remained low and relatively constant. Grazing and haying resulted in a lower probability of noxious grass presence than mowing or disking, but haying and disking were better for inhibiting the presence of noxious forbs. These results show that MCM can be a useful tool for maintaining vegetation quality. The results also point to an important need to understand factors that influence the effects of MCM, including disturbance technique, disturbance frequency, drought, and climate.

Ecological Restoration↗

The role of driving factors in historical and projected carbon dynamics of upland ecosystems in Alaska

It is important to understand how upland ecosystems of Alaska, which are estimated to occupy 84% of the state (i.e., 1,237,774 km 2 ), are influencing and will influence state‐wide carbon (C) dynamics in the face of ongoing climate change. We coupled fire disturbance and biogeochemical models to assess the relative effects of changing atmospheric carbon dioxide (CO 2 ), climate, logging and fire regimes on the historical and future C balance of upland ecosystems for the four main Landscape Conservation Cooperatives (LCCs) of Alaska. At the end of the historical period (1950–2009) of our analysis, we estimate that upland ecosystems of Alaska store ~50 Pg C (with ~90% of the C in soils), and gained 3.26 Tg C/yr. Three of the LCCs had gains in total ecosystem C storage, while the Northwest Boreal LCC lost C (−6.01 Tg C/yr) because of increases in fire activity. Carbon exports from logging affected only the North Pacific LCC and represented less than 1% of the state's net primary production (NPP). The analysis for the future time period (2010–2099) consisted of six simulations driven by climate outputs from two climate models for three emission scenarios. Across the climate scenarios, total ecosystem C storage increased between 19.5 and 66.3 Tg C/yr, which represents 3.4% to 11.7% increase in Alaska upland's storage. We conducted additional simulations to attribute these responses to environmental changes. This analysis showed that atmospheric CO 2 fertilization was the main driver of ecosystem C balance. By comparing future simulations with constant and with increasing atmospheric CO 2 , we estimated that the sensitivity of NPP was 4.8% per 100 ppmv, but NPP becomes less sensitive to CO 2 increase throughout the 21st century. Overall, our analyses suggest that the decreasing CO 2 sensitivity of NPP and the increasing sensitivity of heterotrophic respiration to air temperature, in addition to the increase in C loss from wildfires weakens the C sink from upland ecosystems of Alaska and will ultimately lead to a source of CO 2 to the atmosphere beyond 2100. Therefore, we conclude that the increasing regional C sink we estimate for the 21st century will most likely be transitional.

Alaska↗

Validating a time series of annual grass percent cover in the sagebrush ecosystem

We mapped yearly (2000–2016) estimates of annual grass percent cover for much of the sagebrush ecosystem of the western United States using remotely sensed, climate, and geophysical data in regression-tree models. Annual grasses senesce and cure by early summer and then become beds of fine fuel that easily ignite and spread fire through rangeland systems. Our annual maps estimate the extent of these fuels and can serve as a tool to assist land managers and scientists in understanding the ecosystem’s response to weather variations, disturbances, and management. Validating the time series of annual maps is important for determining the usefulness of the data. To validate these maps, we compare Bureau of Land Management Assessment Inventory and Monitoring (AIM) data to mapped estimates and use a leave-one-out spatial assessment technique that is effective for validating maps that cover broad geographical extents. We hypothesize that the time series of annual maps exhibits high spatiotemporal variability because precipitation is highly variable in arid and semiarid environments where sagebrush is native, and invasive annual grasses respond to precipitation. The remotely sensed data that help drive our regression-tree model effectively measures annual grasses’ response to precipitation. The mean absolute error (MAE) rate varied depending on the validation data and technique used for comparison. The AIM plot data and our maps had substantial spatial incongruence, but despite this, the MAE rate for the assessment equaled 12.62%. The leave-one-out accuracy assessment had an MAE of 8.43%. We quantified bias, and bias was more substantial at higher percent cover. These annual maps can help management identify actions that may alleviate the current cycle of invasive grasses because it enables the assessment of the variability of annual grass − percent cover distribution through space and time, as part of dynamic systems rather than static systems.

Rangeland Ecology and Management↗

Using remote sensing to quantify ecosystem site potential community structure and deviation in the Great Basin, United States

The semi-arid Great Basin region in the Northwest U.S. is impacted by a suite of change agents including fire, grazing, and climate variability to which native vegetation can have low resilience and resistance. Assessing ecosystem condition in relation to these change agents is difficult due to a lack of a consistent and objective Site Potential (SP) information of the conditions biophysically possible at each site. Our objectives were to assess and quantify patterns in ecosystem condition, based on actual fractional component cover and a SP map and to evaluate drivers of change. We used long-term 90th percentile Landsat NDVI(Normalized Difference Vegetation Index) and biophysical variables to produce a map of SP. Ecosystem condition was assessed using two methods, first we integrated fractional components into an index which was regressed against SP. Regression confidence intervals were used to segment the study area into normal, over-, and under-performing relative to SP. Next, the relationships between SP and fractional component cover produced SP expected component cover, from which we mapped the actual cover deviation. Much of the study area is within the range of conditions expected by the SP model, but degraded conditions are more common than those above SP expectations. We found that shrub cover deviation is more positive at higher elevation, while herbaceous cover deviation has the opposite pattern, supporting the hypothesis that more resistant and resilient sites are less likely to change from the shrub dominated legacy. Another key finding was that regions with significant annual herbaceous invasions tend to have lower than expected bare ground and shrub cover.

Great Basin↗