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.     

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.     

Vegetation,Hydrologic, and Erosion Responses of Sagebrush Steppe 9 Yr Following Mechanical Tree Removal

Land managers across the western United States are faced with selecting and applying tree-removal treatments on pinyon (Pinus spp.) and juniper (Juniperus spp.) woodland-encroached sagebrush (Artemisia spp.) rangelands, but current understanding of long-term vegetation and hydrological responses of sagebrush sites to tree removal is inadequate for guiding management. This study applied a suite of vegetation and soil measures (0.5 ? 990 m²), small-plot rainfall simulations (0.5 m²), and overland flow experiments (9 m²) to quantify the effects of mechanical tree removal (tree cutting and mastication) on vegetation, runoff, and erosion at two mid- to late-succession woodland-encroached sagebrush sites in the Great Basin, United States, 9 yr after treatment. Low amounts of hillslope-scale shrub (3 ? 15%) and grass (7 ? 12%) canopy cover and extensive intercanopy (area between tree canopies) bare ground (69 ? 88% bare, 75% of area) in untreated areas at both sites facilitated high levels of runoff and sediment from high-intensity (102 mm ? h^? 1, 45 min) rainfall simulations in interspaces (~ 45 mm runoff, 59 ? 381 g ? m^? 2 sediment) between trees and shrubs and from concentrated overland flow experiments (15, 30, and 45 L ? min^? 1, 8 min each) in the intercanopy (371 ? 501 L runoff, 2 342 ? 3 015 g sediment). Tree cutting increased hillslope-scale density of sagebrush by 5% and perennial grass cover by twofold at one site while tree cutting and mastication increased hillslope-scale sagebrush density by 36% and 16%, respectively, and perennial grass cover by threefold at a second more-degraded (initially more sparsely vegetated) site over nine growing seasons. Cover of cheatgrass (Bromus tectorum L.) was < 1% at the sites pretreatment and 1 ? 7% 9 yr after treatment. Bare ground remained high across both sites 9 yr after tree removal and was reduced by treatments solely at the more degraded site. Increases in hillslope-scale vegetation following tree removal had limited impact on runoff and erosion for rainfall simulations and concentrated flow experiments at both sites due to persistent high bare ground. The one exception was reduced runoff and erosion within the cut treatments for intercanopy plots with cut-downed-trees. The cut-downed-trees provided ample litter cover and tree debris at the ground surface to reduce the amount and erosive energy of concentrated overland flow. Trends in hillslope-scale vegetation responses to tree removal in this study demonstrate the effectiveness of mechanical treatments to reestablish sagebrush steppe vegetation without increasing cheatgrass for mid- to late-succession woodland-encroached sites along the warm-dry to cool-moist soil temperature ? moisture threshold in the Great Basin. Our results indicate improved hydrologic function through sagebrush steppe vegetation recruitment after mechanical tree removal on mid- to late-succession woodlands can require more than 9 yr. We anticipate intercanopy runoff and erosion rates will decrease over time at both sites as shrub and grass cover continue to increase, but follow-up tree removal will be needed to prevent pinyon and juniper recolonization. The low intercanopy runoff and erosion measured underneath isolated cut-downed-trees in this study clearly demonstrate that tree debris following mechanical treatments can effectively limit microsite-scale runoff and erosion over time where tree debris settles in good contact with the soil surface.     

Longer-Term Evaluation of Revegetation of Medusahead-Invaded Sagebrush Steppe

Medusahead (Taeniatherum caput-medusae [L.] Nevski) and other exotic annual grasses have invaded millions of hectares of sagebrush (Artemisia L.) steppe. Revegetation of medusahead-invaded sagebrush steppe with perennial vegetation is critically needed to restore productivity and decrease the risk of frequent wildfires. However, it is unclear if revegetation efforts provide long-term benefits (fewer exotic annuals and more perennials). The limited literature available on the topic questions whether revegetation efforts reduce medusahead abundance beyond 2 or 3 yr. We evaluated revegetation of medusahead-invaded rangelands for 5 yr after seeding introduced perennial bunchgrasses at five locations. We compared areas that were fall-prescribed burned immediately followed by an imazapic herbicide treatment and then seeded with bunchgrasses 1 yr later (imazapic-seed) with untreated controls (control). The imazapic-seed treatment decreased exotic annual grass cover and density. At the end of the study, exotic annual grass cover and density were 2-fold greater in the control compared with the imazapic-seed treatment. The imazapic-seed treatment had greater large perennial bunchgrass cover and density and less annual forb (predominately exotic annuals) cover and density than the untreated control for the duration of the study. At the end of the study, large perennial bunchgrass density average 10 plant ? m^? 2 in the imazapic-seed treatment, which is comparable with intact sagebrush steppe communities. Plant available soil nitrogen was also greater in the imazapic-seed treatment compared with the untreated control for the duration of the study. The results of this study suggest that revegetation of medusahead-invaded sagebrush steppe can provide lasting benefits, including limiting exotic annual grasses.     

Cheatgrass Invasion in Salt Desert Shrublands: Benefits of Postfire Reclamation

In 1998, fires burned more than 11 330 ha of rangeland on Dugway Proving Ground in Utah's west desert. Postfire revegetation was implemented in 2 affected salt desert shrub communities (greasewood; Sarcobatus vermiculatus Hook. and black sagebrush/shadscale; Artemisia nova A. Nels; Atriplex confertifolia Torr. & Frem.) to deter cheatgrass (Bromus tectorum L.) encroachment. We monitored cheatgrass densities for 3 years after the fire in burned drill seeded, burned not-seeded, and unburned plots to assess the rate of invasion and determine the impact on cheatgrass of drill seeding perennial species. Cheatgrass invaded quickly in both shrub sites following the fires. In the greasewood site, drill seeded species germinated but did not establish. This was likely due to a combination of soil salinity and extremely dry weather conditions during the second year of the study. Drill seeded species in the black sagebrush site germinated and established well, resulting in the establishment of 16.5 perennial grasses · m^-2 and 1 356 shrubs · ha^-1. Cheatgrass densities were consistently lower in drill seeded versus not-seeded plots, although these were not always statistically different when Bonferroni comparisons were considered. The initial decrease in cheatgrass densities in drill seeded plots may have resulted from soil disturbance coupled with extremely low precipitation rather than competitive effects. Nevertheless, as seeded species mature and increase their competitive ability, we predict long-term suppression of cheatgrass in the absence of further disturbance.     

Hydrologic and Erosion Responses of Sagebrush Steppe Following Juniper Encroachment,Wildfire, and Tree Cutting

Extensive woodland expansion in the Great Basin has generated concern regarding ecological impacts of tree encroachment on sagebrush rangelands and strategies for restoring sagebrush steppe. This study used rainfall (0.5 m² and 13 m² scales) and concentrated flow simulations and measures of vegetation, ground cover, and soils to investigate hydrologic and erosion impacts of western juniper (Juniperus occidentalis Hook.) encroachment into sagebrush steppe and to evaluate short-term effects of burning and tree cutting on runoff and erosion responses. The overall effects of tree encroachment were a reduction in understory vegetation and formation of highly erodible, bare intercanopy between trees. Runoff and erosion from high-intensity rainfall (102 mm · h^?1, 13 m² plots) were generally low from unburned areas underneath tree canopies (13 mm and 48 g · m^?2) and were higher from the unburned intercanopy (43 mm and 272 g · m^?2). Intercanopy erosion increased linearly with runoff and exponentially where bare ground exceeded 60%. Erosion from simulated concentrated flow was 15- to 25-fold greater from the unburned intercanopy than unburned tree canopy areas. Severe burning amplified erosion from tree canopy plots by a factor of 20 but had a favorable effect on concentrated flow erosion from the intercanopy. Two years postfire, erosion remained 20-fold greater on burned than unburned tree plots, but concentrated flow erosion from the intercanopy (76% of study area) was reduced by herbaceous recruitment. The results indicate burning may amplify runoff and erosion immediately postfire. However, we infer burning that sustains residual understory cover and stimulates vegetation productivity may provide long-term reduction of soil loss relative to woodland persistence. Simply placing cut-downed trees into the unburned intercanopy had minimal immediate impact on infiltration and soil loss. Results suggest cut-tree treatments should focus on establishing tree debris contact with the soil surface if treatments are expected to reduce short-term soil loss during the postcut understory recruitment period.     

Defoliation Effects On Bromus Tectorum Seed Production: Implications For Grazing

Cheatgrass (Bromus tectorum L.) is an invasive annual grass that creates near-homogenous stands in areas throughout the Intermountain sagebrush steppe and challenges successful native plant restoration in these areas. A clipping experiment carried out at two cheatgrass-dominated sites in eastern Oregon (Lincoln Bench and Succor Creek) evaluated defoliation as a potential control method for cheatgrass and a seeding preparation method for native plant reseeding projects. Treatments involved clipping plants at two heights (tall = 7.6 cm, and short = 2.5 cm), two phenological stages (boot and purple), and two frequencies (once and twice), although purple-stage treatments were clipped only once. Treatments at each site were replicated in a randomized complete block design that included a control with no defoliation. End-of-season seed density (seeds · m⁻²) was estimated by sampling viable seeds from plants, litter, and soil of each treatment. Unclipped control plants produced an average of approximately 13 000 and 20 000 seeds · m⁻² at Lincoln Bench and Succor Creek, respectively. Plants clipped short at the boot stage and again 2 wk later had among the lowest mean seed densities at both sites, and were considered the most successful treatments (Lincoln Bench: F_6,45 = 47.07, P < 0.0001; Succor Creek: F_6,40 = 19.60, P < 0.0001). The 95% confidence intervals for seed densities were 123–324 seeds · m⁻² from the Lincoln Bench treatment, and 769–2 256 seeds · m⁻² from the Succor Creek treatment. Literature suggests a maximum acceptable cheatgrass seed density of approximately 330 seeds · m⁻² for successful native plant restoration through reseeding. Thus, although this study helped pinpoint optimal defoliation parameters for cheatgrass control, it also called into question the potential for livestock grazing to be an effective seed-bed preparation technique in native plant reseeding projects in cheatgrass-dominated areas.     

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. We assessed how revegetated community composition influences fire risk at three sites in Columbia National Wildlife Refuge in Grant County, Washington that were revegetated with large bunchgrasses 8 ? 18 years before the study. At each site, five replicates of 10 plots (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, then fire risk was 80%). Preignition, cover of bunchgrasses, cheatgrass, forbs, and surface characteristics were determined for each plot. Fire risk was < 100%. However, fire risk was still relatively high around 73% and did not differ significantly among sites despite differences in cheatgrass and bunchgrass cover, which may have been attributable to other characteristics, such as high total fuels cover (> 80% at all sites) and unvegetated gap cover (soil and soil cryptogams, < 17%). This information can provide guidance for future studies with larger ranges of cover characteristics to develop robust fire risk models, which ultimately will be used to aid rangeland managers who need to specify reduction of fire risk after reestablishing large bunchgrasses in rangelands infested with cheatgrass.     

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.     

Postfire Recovery of Sagebrush Communities: Assessment Using Spot-5 and Very Large-Scale Aerial Imagery

Much interest lies in long-term recovery rates of sagebrush communities after fire in the western United States, as sagebrush communities comprise millions of hectares of rangelands and are an important wildlife habitat. Little is known about postfire changes in sagebrush canopy cover over time, especially at a landscape scale. We studied postfire recovery of shrub canopy cover in sagebrush-steppe communities with the use of spectral mixture analysis. Our study included 16 different fires that burned between 1937 and 2005 and one unburned site at the US Sheep Experiment Station in eastern Idaho. Spectral mixture analysis was used with September 2006 Systeme Pour l’Observation de la Terre-5 (SPOT-5) satellite imagery to estimate percent shrub canopy cover within pixels. Very large-scale aerial (VLSA) imagery with 24-mm resolution was used for training and validation. SPOT-5 image classification was successful and the spectral mixture analysis estimates of percent shrub canopy cover were highly correlated with the shrub canopy cover estimates in the VLSA imagery (R² = 0.82; P < 0.0001). Additional accuracy assessment of shrub classification produced 85% overall accuracy, 98% user’s accuracy, and 78% producer’s accuracy. This successful application of spectral mixture analysis has important implications for the monitoring and assessment of sagebrush-steppe communities. With the use of the percent shrub canopy cover estimates from the classified SPOT-5 imagery, we examined shrub canopy recovery rates since different burn years. With the use of linear-plateau regression, it was determined that shrub cover in mountain big sagebrush (Artemisia tridentata Nutt. subsp. vaseyana [Rydb.] Beetle) communities recovered approximately 27 yr after fire, with an average shrub cover of 38%. These results are consistent with other field-based studies in mountain big sagebrush communities.     

Influence of Land-Use Legacies Following Shrub Reduction and Seeding of Big Sagebrush Sites

Big sagebrush (Artemisia tridentata Nutt.) plant communities often require management to reduce shrub density and rehabilitate understory vegetation. We studied vegetation responses to a two-way chain harrow treatment and broadcast seeding of 12 herbaceous species at eight Wyoming big sagebrush (A. tridentata Nutt. subsp. wyomingensis Beetle & Young) sites. These sites differed in land-use history; five were cultivated for dryland wheat production during the 1950 ? 1980s and then seeded with introduced forage grasses (C-S), while three had not been exposed to this land-use legacy (non C-S). Our objective was to evaluate whether the C-S legacy influences the magnitude of vegetation change following contemporary treatment. Before treatment, C-S sites had lower sagebrush cover, higher dead sagebrush cover, and higher broom snakeweed (Gutierrezia sarothrae [Pursh] Britton & Rusby) cover than adjacent non C-S sites. Plant community change 3 years after treatment, determined with multivariate ordination analysis of species composition, varied between site histories, and response to treatment was most strongly correlated with reductions in sagebrush cover, increases in perennial grasses, and increases in 10 other herbaceous species—including some undesirable species and four that were seeded in 2010. Five years after treatment, mature sagebrush cover remained reduced for both land-use histories, yet density of sagebrush seedlings and broom snakeweed increased in C-S sites during the second and third years after treatment. In addition, perennial forb cover increased for C-S sites, while perennial grass biomass increased for non C-S sites. Our results emphasize that broad variability in plant community responses to sagebrush reduction and seeding is possible within the same ecological site classification and that legacy effects due to the combination of past cultivation and seeding should be considered when planning restoration projects, including the consideration that seeding may not always be necessary on C-S sites.     

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.     

Native Plant Growth and Seedling Establishment in Soils Influenced by Bromus Tectorum

The invasion of 40 million hectares of the American West by cheatgrass (Bromus tectorum L.) has caused widespread modifications in the vegetation of semi-arid ecosystems and increased the frequency of fires. In addition to well-understood mechanisms by which cheatgrass gains competitive advantage, it has been implicated in reducing arbuscular mycorrhizal fungi (AMF) abundance and taxa diversity. We evaluated this possibility at a high elevation site in a two-pronged approach. To test whether cheatgrass changed native AMF communities in ways that affected subsequent native plant growth, we grew cheatgrass and native plants in native soils and then planted native plants into these soils in a greenhouse experiment. We found that cheatgrass-influenced soils did not inhibit native plant growth or AMF sporulation or colonization. To test whether soils in cheatgrass-dominated areas inhibited establishment and growth of native plants, cheatgrass was removed and six seeding combinations were applied. We found that 14.02 ±  seedlings · m⁻² established and perennial native plant cover increased fourfold over the three years of this study. Glyphosate reduced cheatgrass cover to less than 5% in the year it was applied but did not facilitate native plant establishment or growth compared with no glyphosate. We conclude that cheatgrass influence on the soil community does not appear to contribute to its invasion success in these high elevation soils. It appears that once cheatgrass is controlled on sites with sufficient native plant abundance, there may be few lingering effects to inhibit the natural reestablishment of native plant communities.     

The Response of Thurber’s Needlegrass to Fall Prescribed Burning

Thurber’s needlegrass (Achnatherum thurberianum [Piper] Barkworth) is an important component of many sagebrush communities in the Intermountain West. Prescribed fall burning is often implemented in sagebrush plant communities to mimic historic wildfires, improve wildlife habitat, and increase livestock forage production. Burning is used because it shifts dominance from sagebrush to herbaceous vegetation. The effects of prescribed fall burning on Thurber’s needlegrass are largely unexplored. The purpose of this study was to determine the response of Thurber’s needlegrass to prescribed fall burning. A randomized block design was used, and each block consisted of a fall burned and unburned (control) Wyoming big sagebrush (Artemisia tridentata subsp. wyomingensis [Beetle & A. Young] S. L. Welsh)–bunchgrass communities. Response variables measured in the first and second years after burns were Thurber’s needlegrass community foliar cover and density, vegetative and reproductive biomass, photosynthetic rates, tissue carbon (C) and nitrogen (N) content, and N (¹⁵N:¹⁴N) and C (¹³C:¹²C) isotope ratios. Density of Thurber’s needlegrass in both postburn years and cover in the second postburn year were not different between treatments (P > 0.05), but cover was less in the burned than control treatment in the first postburn year (P = 0.008). Carbon isotope ratios in Thurber’s needlegrass differed between the burn (-25.9 ±  SE) and control (-26.3 ±  SE) treatments in the first postburn year (P = 0.019). Nitrogen isotope ratios indicated nitrogen was more available in the burned than control treatment in both years (P < 0.05). Photosynthetic rates of Thurber’s needlegrass were also generally greater in the burned than control treatment (P = 0.045). Our results suggest burning altered the availability of resources to Thurber’s needlegrass plants. Our results also suggest that prescribed fall burning is not detrimental to Thurber’s needlegrass and, thus, can be used as a method to shift dominance from sagebrush to herbaceous vegetation.     

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.     

Evaluating Mechanical Treatments and Seeding of a Wyoming Big Sagebrush Community 10 Yr Post Treatment

Increased cover of perennial grasses and forbs would increase the wildlife and forage value of many Wyoming big sagebrush (Artemisia tridentata ssp. wyomingensis Beetle & Young) communities, as well as increase their resistance to weeds. We compared six mechanical treatments in conjunction with seeding a Wyoming big sagebrush community in northern Utah over a 10-yr period. The treatments included disk plow followed by land imprinter, one-way Ely chain, one- and two-way pipe harrow, all applied in fall, and meadow aerator applied in fall and spring. A mixture of native and introduced grasses and forbs was broadcast seeded at 18.3 kg PLS ha^? 1 after the disk and before the imprinter and all other treatments. The experiment was installed in three randomized blocks, and density and cover data were collected before treatment in 2001 and 1, 2, 5, and 10 yr after treatment. All treatments initially reduced sagebrush and residual herbaceous cover and increased seeded species cover compared with the untreated control. By 10 yr after treatment, sagebrush cover was 24.5% ± 0.35% on the control, 1.6% ± 0.28% on the disk imprinter treatment, and 11.7% ± 0.79% on all other treatments. At that time, seeded grass cover was 16.5% ± 1.22% on the disk imprinter treatment and an average of 2% ± 0.1% on all other mechanical treatments. Sagebrush seedlings were recruited in all of the mechanical treatments, but least in the disk imprinter treatment. After 10 yr, the untreated control was dominated by decadent sagebrush and rabbitbrush, the disk imprinter treatment was dominated by seeded perennial grasses, and the other mechanical treatments shared dominance of sagebrush and native perennial grasses. Mechanical treatments changed the composition of this community while retaining sagebrush, but greatest understory increases were associated with greatest control of sagebrush and establishment of seeded species by disk imprinting.     

Longer-Term Evaluation of Sagebrush Restoration After Juniper Control and Herbaceous Vegetation Trade-offs

Degradation of shrublands around the world from altered fire regimes, overutilization, and anthropogenic disturbance has resulted in a widespread need for shrub restoration. In western North America, reestablishment of mountain big sagebrush (Artemisia tridentata Nutt. ssp. vaseyana [Rydb.] Beetle) is needed to restore ecosystem services and function. Western juniper (Juniperus occidentalis ssp. occidentalis Hook) encroachment is a serious threat to mountain big sagebrush communities in the northern Great Basin and Columbia Plateau. Juniper trees can be controlled with fire; however, sagebrush recovery may be slow, especially if encroachment largely eliminated sagebrush before juniper control. Short-term studies have suggested that seeding mountain big sagebrush after juniper control may accelerate sagebrush recovery. Longer-term information is lacking on how sagebrush recovery progresses and if there are trade-offs with herbaceous vegetation. We compared seeding and not seeding mountain big sagebrush after juniper control (partial cutting followed with burning) in fully developed juniper woodlands (i.e., sagebrush had been largely excluded) at five sites, 7 and 8 yr after seeding. Sagebrush cover averaged ~ 30% in sagebrush seeded plots compared with ~ 1% in unseeded plots 8 yr after seeding, thus suggesting that sagebrush recovery may be slow without seeding after juniper control. Total herbaceous vegetation, perennial grass, and annual forb cover was less where sagebrush was seeded. Thus, there is a trade-off with herbaceous vegetation with seeding sagebrush. Our results suggest that seeding sagebrush after juniper control can accelerate the recovery of sagebrush habitat characteristics, which is important for sagebrush-associated wildlife. We suggest land manager and restoration practitioners consider seeding sagebrush and possibly other shrubs after controlling encroaching trees where residual shrubs are lacking after control.     

Soil Seed Banks of the Exotic Annual Grass Bromus rubens on a Burned Desert Landscape

Red brome (Bromus rubens), an exotic annual grass, can dominate soil seed banks and poses serious threats to mature native plant communities in the Mojave Desert by competing with native species and providing fine fuels that facilitate widespread wildfire. By exploring how seed bank density and composition in burned areas change over time since fire (TSF), we can improve our understanding of how the seed banks are affected by fire. Samples of the 5-cm-deep soil seed bank were collected from two microsites (under shrubs, in open interspaces) within paired burned and unburned areas on 12 fires ranging from 5–31 yr TSF. Seed bank samples were assayed using the emergence method and seed densities were compared among TSFs, burn status (burned, unburned), and microsites for the species that emerged. Red brome soil seed bank density was spatially variable and TSF rarely predicted abundance. Overall, undershrub seed densities did not differ between burned and unburned areas. However, at some fire sites, seed densities in interspaces were greater in burned than unburned areas. Although native seed densities were low overall, they did not appear to differ according to burn status. Studies have shown that red brome plant and seed bank densities can be greatly reduced immediately after fire. Management efforts that focus on this initial colonization window may be able to take advantage of diminished red brome seed densities to limit its reestablishment while facilitating the establishment of native species. However, this window is brief, as our findings indicate that once reestablished, red brome soil seed densities in burned areas can be similar to those in unburned areas within 5 yr.