Can Imazapic Increase Native Species Abundance in Cheatgrass (Bromus tectorum) Invaded Native Plant Communities?

Native plant communities invaded by cheatgrass (Bromus tectorum L.) are at risk of unnatural high intensity fires and conversion to cheatgrass monocultures. Management strategies that reduce cheatgrass abundance may potentially allow native species to expand and minimize further cheatgrass invasion. We tested whether the selective herbicide imazapic is effective in reducing cheatgrass and “releasing” native species in a semiarid grassland and shrub steppe in north-central Oregon. The experiment consisted of a completely randomized design with two treatments (sprayed with 70 g ai · ha^?1 of imazapic and unsprayed) and three replicates of each treatment applied to either 2.5 or 4 ha plots. We repeated this experiment in three different sites dominated by the following native species: 1) bluebunch wheatgrass (Pseudoroegneria spicata [Pursh] A. Löve ssp. spicata) and needle and thread (Hesperostipa comata [Trin. & Rupr.] Barkworth), 2) needle and thread and Sandberg bluegrass (Poa secunda J. Presl), and 3) big sagebrush (Artemisia tridentata Nutt.). Nested frequency of all plant species in 1-m² quadrats was collected for 1  yr pretreatment and 4  yr posttreatment. In all three sites, cheatgrass frequencies were significantly lower in sprayed plots than unsprayed plots for 3–4  yr posttreatment (P < 0.1). Other annual plant species were also impacted by imazapic, but the effects were highly variable by species and site. Only two native perennial species, hoary tansyaster (Machaeranthera canescens [Pursh] Gray) and big sagebrush, increased in sprayed plots, and increases occurred only at two sites. These results suggest that a short-term reduction in cheatgrass alone is not an effective strategy for increasing the abundance of most native perennial plant species.     

Understory Cover Responses to Piñon–Juniper Treatments Across Tree Dominance Gradients in the Great Basin

Piñon (Pinus spp.) and juniper (Juniperus spp.) trees are reduced to restore native vegetation and avoid severe fires where they have expanded into sagebrush (Artemisia tridentata Nutt.) communities. However, what phase of tree infilling should treatments target to retain desirable understory cover and avoid weed dominance? Prescribed fire and tree felling were applied to 8–20-ha treatment plots at 11 sites across the Great Basin with a tree-shredding treatment also applied to four Utah sites. Treatments were applied across a tree infilling gradient as quantified by a covariate tree dominance index (TDI = tree cover/&lsqb;tree + shrub + tall perennial grass cover]). Mixed model analysis of covariance indicated that treatment × covariate interactions were significant (P &spilt; 0.05) for most vegetation functional groups 3 yr after treatment. Shrub cover was most reduced with fire at any TDI or by mechanical treatment after infilling resulted in over 50% shrub cover loss (TDI &spigt; 0.4). Fire increased cheatgrass (Bromus tectorum L.) cover by an average of 4.2% for all values of TDI. Cutting or shredding trees generally produced similar responses and increased total perennial herbaceous and cheatgrass cover by an average of 10.2% and 3.8%, at TDIs ≥ 0.35 and ≥ 0.45. Cheatgrass cover estimated across the region was &spilt; 6% after treatment, but two warmer sites had high cheatgrass cover before (19.2% and 27.2%) and after tree reduction (26.6% and 50.4%). Fuel control treatments are viable management options for increasing understory cover across a range of sites and tree cover gradients, but should be accompanied by revegetation on warmer sites with depleted understories where cheatgrass is highly adapted. Shrub and perennial herbaceous cover can be maintained by mechanically treating at lower TDI. Perennial herbaceous cover is key for avoiding biotic and abiotic thresholds in this system through resisting weed dominance and erosion.     

Prediction of Cheatgrass Field Germination Potential Using Wet Thermal Accumulation

Invasion and dominance of weedy species is facilitated or constrained by environmental and ecological factors that affect resource availability during critical life stages. We compared the relative effects of season, annual weather, site, and disturbance on potential cheatgrass (Bromus tectorum L.) germination in big sagebrush (Artemisia tridentata Nutt.) communities. Soil water status and temperature in the seedbed were measured continuously for 4 years on 9 big sagebrush sites in Nevada and Utah. Field plots at lower-, middle-, and upper-elevation sites were either undisturbed, or were burned, sprayed with herbicide, or both sprayed and burned. Spraying removed perennial herbaceous vegetation, whereas burning removed sagebrush. We used thermal-germination data from laboratory incubation studies of 18 cheatgrass seedlots and field soil moisture and temperature measurements to model and predict potential germination in the field plots for periods when seedbeds were continuously wet (above -0.5, -1, or -1.5 MPa) and across intermittent wet and dry periods. Season had the greatest effect on potential cheatgrass germination, followed by annual weather, and site variables (elevation and location); the effects of disturbance were minimal. Potential germination was predicted for most sites and years in spring, a majority of sites and years in fall, and few sites or years in winter. Even though disturbance has limited effects on potential germination, it can increase cheatgrass invasion and dominance by reducing perennial herbaceous species resource use and allowing increased cheatgrass growth and reproduction.     

Revegetation of Medusahead-Invaded Sagebrush Steppe

Medusahead (Taeniatherum caput-medusae [L.] Nevski) is an exotic annual grass invading western rangelands. Invasion by medusahead is problematic because it decreases livestock forage production, degrades wildlife habitat, reduces biodiversity, and increases fire frequency. Revegetation of medusahead-invaded sagebrush steppe is needed to increase ecosystem and economic productivity. Most efforts to revegetate medusahead-infested plant communities are unsuccessful because perennial bunchgrasses rarely establish after medusahead control. The effects of prescribed burning (spring or fall), fall imazapic application, and their combinations were evaluated for medusahead control and the establishment of seeded large perennial bunchgrasses. One growing season after treatments were applied, desert wheatgrass (Agropyron desertorum [Fisch. ex Link] Schult.) and squirreltail (Elymus elymoides [Raf.] Swezey) were drill seeded into treatment plots, except for the control treatment. Vegetation characteristics were measured for 2 yr postseeding (second and third year post-treatment). Medusahead was best controlled when prescribed burned and then treated with imazapic (P < 0.05). These treatments also had greater large perennial bunchgrass cover and density compared to other treatments (P < 0.05). The prescribed burned followed by imazapic application had greater than 10- and 8-fold more perennial bunchgrass cover and density than the control treatment, respectively. Prescribed burning, regardless of season, was not effective at controlling medusahead or promoting establishment of perennial bunchgrasses. The results of this study question the long-term effectiveness of using imazapic in revegetation efforts of medusahead-infested sagebrush steppe without first prescribed burning the infestation. Effective control of medusahead appears to be needed for establishment of seeded perennial bunchgrasses. The results of this study demonstrate that seeding desert wheatgrass and squirreltail can successfully revegetate rangeland infested with medusahead when medusahead has been controlled with prescribed fire followed by fall application of imazapic.     

Effects of Nitrogen Availability and Cheatgrass Competition on the Establishment of Vavilov Siberian Wheatgrass

Cheatgrass (Bromus tectorum L.) is the most widespread invasive weed in sagebrush ecosystems of North America. Restoration of perennial vegetation is difficult and land managers have often used introduced bunchgrasses to restore degraded sagebrush communities. Our objective was to evaluate the potential of ‘Vavilov’ Siberian wheatgrass (Agropyron fragile [Roth] P. Candargy) to establish on cheatgrass-dominated sites. We examined Vavilov establishment in response to different levels of soil nitrogen availability by adding sucrose to the soil to promote nitrogen (N) immobilization and examined cheatgrass competition by seeding different levels of cheatgrass. We used a blocked split-split plot design with two sucrose levels (0 and 360 g · m⁻²), two levels of Vavilov (0 and 300 seeds · m⁻²), and five levels of cheatgrass (0, 150, 300, 600, and 1 200 seeds · m⁻²). Seeding was conducted in fall 2003 and 2004, and measurements were taken in June 2004, 2005, and 2006. Sucrose addition decreased availability of soil nitrate but not orthophosphate. In the first year after seeding, sucrose reduced cheatgrass density by 35% and decreased both cheatgrass biomass per square meter and seed production per square meter by 67%. These effects were temporary, and by the second year after seeding, there was a sevenfold increase in cheatgrass density. As a result, the effects of sucrose addition were no longer significant. Sucrose affected Vavilov growth, but not density, during the first year after seeding. Vavilov density decreased as cheatgrass seeding density increased. Short-term reductions in N or cheatgrass seed supply did not have long-term effects on cheatgrass and did not increase Vavilov establishment. Longer-term reductions in soil N, higher seeding densities, or more competitive plant materials are necessary to revegetate areas dominated by cheatgrass.     

Invasion is Contingent on Species Assemblage and Invasive Species Identity in Experimental Rehabilitation Plots

Ecological studies often suggest that diverse communities are most resistant to invasion by exotic plants, but relatively few local species may be available to a rehabilitation practitioner. We examine the ability of monocultures and diverse assemblages to resist invasion by an exotic annual grass (cheatgrass) and an exotic biennial forb (dyer's woad) in experimental rehabilitation plots. We constructed seven assemblages that included three monocultures of grass, forb, or shrub; three four-species mixtures of grasses, forbs, or shrubs; and a three-species mixture of one species from each growth form in an experimental field setting to test resistance to invasion. Assemblages were seeded with cheatgrass and dyer's woad for two consecutive years and quantified as biomass and density of individuals from each exotic species. Soil NO₃^- and leaf-area index were examined as predictors of invasive plant abundance. Cheatgrass invasion was greatest in forb and shrub assemblages, and least in mixed grass or grass monoculture; dyer's woad invasion was greatest into mixed grass or grass monoculture, but least into monoculture or mixed-species assemblages composed of forbs or shrubs. The community composed of grasses, forbs, and shrubs suppressed invasion by both species. Consequently, assemblages were most resistant to invasion by species of the same growth form. Moreover, these monocultures and mixtures were generally similar in conferring resistance to invasion, but a monoculture of big sagebrush was more resistant than a mixture of shrubs. Soil NO₃^- was correlated with invasion by cheatgrass, whereas LAI was correlated with invasion by dyer's woad, suggesting these species were more limited by belowground and aboveground resources, respectively. Overall, increasing diversity with limited species did not necessarily enhance resistance to invasion.     

Prescribed Summer Fire and Seeding Applied to Restore Juniper-Encroached and Exotic Annual Grass-Invaded Sagebrush Steppe

Western juniper (Juniperus occidentalis Hook.) encroachment and exotic annual grass (medusahead [Taeniatherum caput-medusae L. Nevski] and cheatgrass [Bromus tectorum L.]) invasion of sagebrush (Artemisia L.) communities decrease ecosystem services and degrade ecosystem function. Traditionally, these compositional changes were largely confined to separate areas, but more sagebrush communities are now simultaneously being altered by juniper and exotic annual grasses. Few efforts have evaluated attempts to restore these sagebrush communities. The Crooked River National Grassland initiated a project to restore juniper-encroached and annual grass-invaded sagebrush steppe using summer (mid-July) applied prescribed fires and postfire seeding. Treatments were unburned, burned, burned and seeded with a native seed mix, and burned and seeded with an introduced seed mix. Prescribed burning removed all juniper and initially reduced medusahead cover but did not influence cheatgrass cover. Neither the native nor introduced seed mix were successful at increasing large bunchgrass cover, and 6 yr post fire, medusahead cover was greater in burned treatments compared with the unburned treatment. Large bunchgrass cover and biological soil crusts were less in treatments that included burning. Exotic forbs and bulbous bluegrass (Poa bulbosa L.), an exotic grass, were greater in burned treatments compared with the unburned treatment. Sagebrush communities that are both juniper encroached and exotic annual grass invaded will need specific management of both juniper and annual grasses. We suggest that additional treatments, such as pre-emergent herbicide control of annuals and possibly multiple seeding events, are necessary to restore these communities. We recommend an adaptive management approach in which additional treatments are applied on the basis of monitoring data.     

Disturbance Type and Sagebrush Community Type Affect Plant Community Structure After Shrub Reduction

Treatments to reduce shrub cover are commonly implemented with the objective of shifting community structure away from shrub dominance and toward shrub and perennial grass codominance. In sagebrush (Artemisia L.) ecosystems, shrub reduction treatments have had variable effects on target shrubs, herbaceous perennials, and non-native annual plants. The factors mediating this variability are not well understood. We used long-term data from Utah’s Watershed Restoration Initiative project to assess short-term (1 − 4 yr post-treatment) and long-term (5 − 12 yr post-treatment) responses of sagebrush plant communities to five shrub reduction treatments at 94 sites that span a range of abiotic conditions and sagebrush community types. Treatments were pipe harrow with one or two passes, aerator, and fire with and without postfire seeding. We analyzed effect sizes (log of response ratio) to assess responses of sagebrush, perennial and annual grasses and forbs, and ground cover to treatments. Most treatments successfully reduced sagebrush cover over the short and long term. All treatments increased long-term perennial grass cover in Wyoming big sagebrush (A. tridentata Nutt. ssp. wyomingensis Beetle & Young) communities, but in mountain big sagebrush (ssp. vaseyana [Rydb.] Beetle) communities, perennial grasses increased only when seeded after fire. In both sagebrush communities, treatments generally resulted in short-term, but not long-term, increases in perennial forb cover. Annual grasses (largely invasive cheatgrass, Bromus tectorum L.) increased in all treatments on sites dominated by mountain big sagebrush but stayed constant or decreased on sites dominated by Wyoming big sagebrush. This result was unexpected because sites dominated by Wyoming big sagebrush are typically thought to be less resilient to disturbance and less resistant to invasion than sites dominated by mountain big sagebrush. Together, these results indicate some of the benefits, risks, and contingent outcomes of sagebrush reduction treatments that should be considered carefully in any future decisions about applying such treatments.     

Herbaceous Biomass Response to Prescribed Fire in Juniper-Encroached Sagebrush Steppe

Western juniper (Juniperus occidentalis Hook.) has expanded into sagebrush steppe plant communities the past 130 ? 150 yr in the northern Great Basin. The increase in juniper reduces herbage and browse for livestock and big game. Information on herbaceous yield response to juniper control with fire is limited. We measured herbaceous standing crop and yield by life form in two mountain big sagebrush communities (MTN1, MTN2) and a Wyoming/basin big sagebrush (WYOBAS) community for 6 yrs following prescribed fire treatments to control western juniper. MTN1 and WYOBAS communities were early-successional (phase 1) and MTN2 communities were midsuccessional (phase 2) woodlands before treatment. Prescribed fires killed all juniper and sagebrush in the burn units. Total herbaceous and perennial bunchgrass yields increased 2 to 2.5-fold in burn treatments compared with unburned controls. Total perennial forb yield did not differ between burns and controls in all three plant communities. However, tall perennial forb yield was 1.6- and 2.5-fold greater in the WYOBAS and MTN2 burned sites than controls. Mat-forming perennial forb yields declined by 80 ? 90% after burning compared with controls. Cheatgrass yield increased in burned WYOBAS and MTN2 communities and at the end of the study represented 10% and 22% of total yield, respectively. Annual forbs increased with burning and were mainly composed of native species in MTN1 and MTN2 communities and non-natives in WYOBAS communities. Forage availability for livestock and wild ungulates more than doubled after burning. The additional forage provided on burned areas affords managers greater flexibility to rest and treat additional sagebrush steppe where juniper is expanding, as well as rest or defer critical seasonal habitat for wildlife.     

Models for Predicting Fuel Consumption in Sagebrush-Dominated Ecosystems

Fuel consumption predictions are necessary to accurately estimate or model fire effects, including pollutant emissions during wildland fires. Fuel and environmental measurements on a series of operational prescribed fires were used to develop empirical models for predicting fuel consumption in big sagebrush (Artemisia tridentata Nutt.) ecosystems. Models are proposed for predicting fuel consumption during prescribed fires in the fall and the spring. Total prefire fuel loading ranged from 5.3–23.6 Mg · ha^?1; between 32% and 92% of the total loading was composed of live and dead big sagebrush. Fuel consumption ranged from 0.8–22.3 Mg · ha^?1, which equates to 11–99% of prefire loading (mean = 59%). Model predictors include prefire shrub loading, proportion of area burned, and season of burn for shrub fuels (R² = 0.91). Models for predicting proportion of area burned for spring and fall fires were also developed (R² = 0.64 and 0.77 for spring and fall fire models, respectively). Proportion of area burned, an indicator of the patchiness of the fire, was best predicted from the coverage of the herbaceous vegetation layer, wind speed, and slope; for spring fires, day-of-burn 10-h woody fuel moisture content was also an important predictor variable. Models predicted independent shrub consumption measurements within 8.1% (fall) and 12.6% (spring) for sagebrush fires.     

Shrub Microsite Influences Post-Fire Perennial Grass Establishment

Woody plants can cause localized increases in resources (i.e., resource islands) that can persist after fire and create a heterogeneous environment for restoration. Others have found that subcanopies have increased soil organic matter, nitrogen, and carbon and elevated post-fire soil temperature. We tested the hypothesis that burned sagebrush subcanopies would have increased seedling establishment and performance of post-fire seeded perennial bunchgrasses compared to burned interspaces. We used a randomized complete block design with five study sites located in southeast Oregon. The area was burned in a wildfire (2007) and reseeded in the same year with a seed mix that included non-native and native perennial bunchgrasses. Seedling density, height, and reproductive status were measured in October 2008 in burned subcanopy and interspace microsites. Non-native perennial grasses had greater densities than native species (P < 0.001) and were six times more abundant in burned subcanopies compared to burned interspaces (P < 0.001). Density of natives in burned subcanopies was 24-fold higher than burned interspaces (P = 0.043). Seedlings were taller in burned subcanopies compared to burned interspaces (P = 0.001). Subcanopy microsites had more reproductive seedlings than interspace microsites (P < 0.001). Our results suggest that under the fire conditions examined in this study, pre-burn shrub cover may be important to post-fire restoration of perennial grasses. Determining the mechanisms responsible for increased seeding success in subcanopy microsites may suggest tactics that could be used to improve existing restoration technologies.     

Resilience and Resistance of Sagebrush Ecosystems: Implications for State and Transition Models and Management Treatments

In sagebrush ecosystems invasion of annual exotics and expansion of piñon (Pinus monophylla Torr. and Frem.) and juniper (Juniperus occidentalis Hook., J. osteosperma &lsqb;Torr.] Little) are altering fire regimes and resulting in large-scale ecosystem transformations. Management treatments aim to increase resilience to disturbance and enhance resistance to invasive species by reducing woody fuels and increasing native perennial herbaceous species. We used Sagebrush Steppe Treatment Evaluation Project data to test predictions on effects of fire vs. mechanical treatments on resilience and resistance for three site types exhibiting cheatgrass (Bromus tectorum L.) invasion and/or piñon and juniper expansion: 1) warm and dry Wyoming big sagebrush (WY shrub); 2) warm and moist Wyoming big sagebrush (WY PJ); and 3) cool and moist mountain big sagebrush (Mtn PJ). Warm and dry (mesic/aridic) WY shrub sites had lower resilience to fire (less shrub recruitment and native perennial herbaceous response) than cooler and moister (frigid/xeric) WY PJ and Mtn PJ sites. Warm (mesic) WY Shrub and WY PJ sites had lower resistance to annual exotics than cool (frigid to cool frigid) Mtn PJ sites. In WY shrub, fire and sagebrush mowing had similar effects on shrub cover and, thus, on perennial native herbaceous and exotic cover. In WY PJ and Mtn PJ, effects were greater for fire than cut-and-leave treatments and with high tree cover in general because most woody vegetation was removed increasing resources for other functional groups. In WY shrub, about 20% pretreatment perennial native herb cover was necessary to prevent increases in exotics after treatment. Cooler and moister WY PJ and especially Mtn PJ were more resistant to annual exotics, but perennial native herb cover was still required for site recovery. We use our results to develop state and transition models that illustrate how resilience and resistance influence vegetation dynamics and management options.     

Effects of Sagebrush Restoration and Conifer Encroachment on Small Mammal Diversity in Sagebrush Ecosystem

Conifer encroachment in sagebrush ecosystems reduces habitat heterogeneity, niche space, and resource availability, all of which negatively affect many wildlife populations. Sagebrush restoration is recommended as a management action to mitigate conifer encroachment and restore wildlife across millions of hectares in the Great Basin. Despite this recommendation, the effects of conifer encroachment and sagebrush restoration are unknown for most wildlife species. Small nonvolant mammal communities include keystone species, consumers and prey; facilitate energy flow and ecological function; and provide important ecological goods and services. We assessed causal relationships between conifer encroachment and sagebrush restoration (conifer removal and seeding native plants) on small mammal communities over 11 yr using a Before-After-Control–Impact design. Sagebrush habitat supported an additional small mammal species, twice the biomass, and nearly three times higher densities than conifer-encroached habitat. Sagebrush restoration increased shrub cover, decreased tree cover, and density but failed to increase native herbaceous plant density. Restoration caused a large increase in the non-native, invasive annual cheatgrass (Bromus tectorum L.). Counter to prediction, small mammal diversity did not increase in response to sagebrush restoration, but restoration maintained small mammal density in the face of ongoing conifer encroachment. Piñon mice (Peromyscus truei), woodland specialists with highest densities in conifer-encroached habitat, were negatively affected by sagebrush restoration. Increasing cheatgrass due to sagebrush restoration may not negatively impact small mammal diversity, provided cheatgrass density and cover do not progress to a monoculture and native vegetation is maintained. The consequences of conifer encroachment, a long-term, slow-acting impact, far outweigh the impacts of sagebrush restoration, a short-term, high-intensity impact, on small mammal diversity. Given the ecological importance of small mammals, maintenance of small mammal density is a desirable outcome for sagebrush restoration.     

Crested Wheatgrass Control and Native Plant Establishment in Utah

Effective control methods need to be developed to reduce crested wheatgrass (Agropyron cristatum [L.] Gaertner) monocultures and promote the establishment of native species. This research was designed to determine effective ways to reduce crested wheatgrass and establish native species while minimizing weed invasion. We mechanically (single- or double-pass disking) and chemically (1.1 L · ha^?1 or 3.2 L · ha^?1 glyphosate–Roundup Original Max) treated two crested wheatgrass sites in northern Utah followed by seeding native species in 2005 and 2006. The study was conducted at each site as a randomized block split plot design with five blocks. Following wheatgrass-reduction treatments, plots were divided into 0.2-ha subplots that were either unseeded or seeded with native plant species using a Truax Rough Rider rangeland drill. Double-pass disking in 2005 best initially controlled wheatgrass and decreased cover from 14% to 6% at Lookout Pass and from 14% to 4% at Skull Valley in 2006. However, crested wheatgrass recovered to similar cover percentages as untreated plots 2–3 yr after wheatgrass-reduction treatments. At the Skull Valley site, cheatgrass cover decreased by 14% on herbicide-treated plots compared to an increase of 33% on mechanical-treated plots. Cheatgrass cover was also similar on undisturbed and treated plots 2 yr and 3 yr after wheatgrass-reduction treatments, indicating that wheatgrass recovery minimized any increases in weed dominance as a result of disturbance. Native grasses had high emergence after seeding, but lack of survival was associated with short periods of soil moisture availability in spring 2007. Effective wheatgrass control may require secondary treatments to reduce the seed bank and open stands to dominance by seeded native species. Manipulation of crested wheatgrass stands to restore native species carries the risk of weed invasion if secondary treatments effectively control the wheatgrass and native species have limited survival due to drought.     

Cattle Grazing and Vegetation Succession on Burned Sagebrush Steppe

There is limited information about the effects of cattle grazing to longer-term plant community composition and herbage production following fire in sagebrush steppe. This study evaluated vegetation response to cattle grazing over 7 yr (2007–2013) on burned Wyoming big sagebrush (Artemisia tridentata ssp. wyomingensis [Beetle & Young] Welsh) steppe in eastern Oregon. Treatments, replicated four times and applied in a randomized complete block design, included no grazing on burned (nonuse) and unburned (control) sagebrush steppe; and cattle grazing at low (low), moderate (moderate), and high (high) stocking on burned sagebrush steppe. Vegetation dynamics were evaluated by quantifying herbaceous (canopy and basal cover, density, production, reproductive shoot weight) and shrub (canopy cover, density) response variables. Aside from basal cover, herbaceous canopy cover, production, and reproduction were not different among low, moderate, and nonuse treatments. Perennial bunchgrass basal cover was about 25% lower in the low and moderate treatments than the nonuse. Production, reproductive stem weight, and perennial grass basal cover were greater in the low, moderate, and nonuse treatments than the control. The high treatment had lower perennial bunchgrass cover (canopy and basal) and production than other grazed and nonuse treatments. Bunchgrass density remained unchanged in the high treatment, not differing from other treatments, and reproductive effort was comparable to the other treatments, indicating these areas are potentially recoverable by reducing stocking. Cover and production of Bromus tectorum L. (cheatgrass) did not differ among the grazed and nonuse treatments, though all were greater than the control. Cover and density of A.t. spp. wyomingensis did not differ among the burned grazed and nonuse treatments and were less than the control. We concluded that light to moderate stocking rates are compatible to sustainable grazing of burned sagebrush steppe rangelands.     

Postfire Succession in Big Sagebrush Steppe With Livestock Grazing

Prescribed fire in rangeland ecosystems is applied for a variety of management objectives, including enhancing productivity of forage species for domestic livestock. In the big sagebrush (Artemisia tridentata Nutt.) steppe of the western United States, fire has been a natural and prescribed disturbance, temporarily shifting vegetation from shrub–grass codominance to grass dominance. There is limited information on the impacts of grazing to community dynamics following fire in big sagebrush steppe. This study evaluated cattle grazing impacts over four growing seasons after prescribed fire on Wyoming big sagebrush (Artemisia tridentata subsp. Wyomingensis [Beetle & Young] Welsh) steppe in eastern Oregon. Treatments included no grazing on burned and unburned sagebrush steppe, two summer-grazing applications after fire, and two spring-grazing applications after fire. Treatment plots were burned in fall 2002. Grazing trials were applied from 2003 to 2005. Vegetation dynamics in the treatments were evaluated by quantifying herbaceous canopy cover, density, annual yield, and perennial grass seed yield. Seed production was greater in the ungrazed burn treatments than in all burn–grazed treatments; however, these differences did not affect community recovery after fire. Other herbaceous response variables (cover, density, composition, and annual yield), bare ground, and soil surface litter did not differ among grazed and ungrazed burn treatments. All burn treatments (grazed and ungrazed) had greater herbaceous cover, herbaceous standing crop, herbaceous annual yield, and grass seed production than the unburned treatment by the second or third year after fire. The results demonstrated that properly applied livestock grazing after low-severity, prescribed fire will not hinder the recovery of herbaceous plant communities in Wyoming big sagebrush steppe.     

Hydrologic Impacts of Mechanical Seeding Treatments on Sagebrush Rangelands

In and around the Great Basin, United States, restoration of shrub steppe vegetation is needed where rangelands are transitioning to annual grasslands. Mechanical seedbed preparation can aid native species recovery by reducing annual grass competition. This study was designed to investigate the nature and persistence of hydrologic and erosion impacts caused by different mechanical rangeland seeding treatments and to identify interactions between such impacts and related soil and vegetation properties. A cheatgrass (Bromus tectorum L.)–dominated site was burned and seeded with native grasses and shrubs in the fall of the year. An Amazon-drill and a disk-chain seeder were used to provide varying levels of surface soil disturbance. An undisturbed broadcast seeding was used as a control. Simulated rainfall was applied to 6 large (32.5-m²) plots per treatment over 3 growing seasons at a rate of 63.5 mm · h^-1. Rainfall was applied for 60 minutes under dry antecedent moisture conditions and for 30 minutes, 24 hours later under wet antecedent moisture conditions. The disk-chain created the largest reduction in infiltration and increase in sediment yield, which lasted for 3 growing seasons posttreatment. The Amazon-drill had a lesser impact, which was insignificant after the second growing season posttreatment. Surface soil properties showed little correlation with treatment-induced hydrologic and erosion impacts. Hydrologic recovery was strongly correlated with litter dynamics. The seeding treatments were unsuccessful at establishing seeded plant species, and the site once again became dominated by cheatgrass. A continuous upward trend in biomass production and surface litter cover was observed for all treatments between the beginning and end of the study because of cheatgrass invasion. Although the initial goal of using mechanical seeding treatments to enhance recovery of native grass species failed, cheatgrass production provided sufficient biomass to rapidly replenish surface litter cover necessary for rapid hydrologic stability of the site.     

A Comparison of Bromus tectorum Growth and Mycorrhizal Colonization in Salt Desert vs. Sagebrush Habitats

Cheatgrass (Bromus tectorum) has recently invaded marginal low-elevation salt desert habitats across the Great Basin. We tested the hypothesis that cheatgrass seed produced in populations from the more stressful salt desert vs. upland sagebrush habitats should grow differently in salt desert soils compared to adjacent upland sagebrush soil, and vice versa. We evaluated growth, incidence of flowering, and arbuscular mycorrhizal fungi (AMF) colonization of plants grown in the soils from which their seeds were collected vs. in the reciprocal soils from the nearest sagebrush or salt desert site in three large basins in northern Nevada. Simultaneously we measured nutrient cations, available nitrogen and phosphorus, percent carbon and nitrogen, texture, and dry-down characteristics in all soils. We found that salt desert soils were generally more nutrient poor and more saline than their upland (sagebrush) counterparts; salt desert soils also generally had a higher percentage of sand compared to their upland counterparts and were consistently drier. The most dramatic plant responses to soil and seed source were 1) lower aboveground biomass of mature plants in most salt desert soils compared to sagebrush soils, or lower biomass in plants grown from salt desert seed; 2) lower root:shoot ratios in plants grown in salt desert soil across two of three basins, irrespective of seed source; 3) a higher percentage of flowering individuals from salt desert seed sources at harvest, irrespective of soil source; 4) depressed AMF colonization of plants in salt desert soils; and 5) strong influence exerted by seed source on AMF, whereby sagebrush-originating plants grown in sagebrush soils had greater AMF colonization compared to salt desert soils but salt desert-originating seedlings had very low AMF colonization rates irrespective of soil source. These results suggest that both population level and soil-based controls are important as this widespread weed moves into marginal habitat.     

Postfire Invasion Potential of Rush Skeletonweed (Chondrilla Juncea)

North American sagebrush steppe communities have been transformed by the introduction of invasive annual grasses and subsequent increase in fire size and frequency. We examined the effects of wildfires and environmental conditions on the ability of rush skeletonweed (Chondrilla juncea L.), a perennial Eurasian composite, to invade degraded sagebrush steppe communities, largely dominated by cheatgrass (Bromus tectorum L.). Recruitment of rush skeletonweed from seed and root buds was investigated on 11 burned and unburned plot pairs on Idaho's Snake River Plain following summer 2003 wildfires. Emergence from soil seedbanks was similar on burned and unburned plots in 2003 and 2004 (P = 0.37). Soils from recently burned plots (P = 0.05) and sterilized field soil (P &spilt; 0.01) supported greater emergence than did unburned field soils when rush skeletonweed seeds were mixed into the soils in the laboratory. These decreases may indicate susceptibility of this exotic invasive to soil pathogens present in field soils. Seeds in bags placed on field soil in late October 2003 reached peak germination by mid-January 2004 during a wet period; 1% remained viable by August 2004. Seedling emergence from sown plots or the native seedbank and establishment of new rosettes from root sprouts in 2003–2005 indicate that seed germination of rush skeletonweed on the Snake River Plain may be facultative, occurring in fall or spring if soil moisture is adequate, although many germinants may not survive. Stand development results primarily from root sprouting. Establishment from seed is episodic but provides for dispersal, with increasing fire frequency and size expanding the areas of disturbance available for new invasions.