Fire Return Interval and Season of Fire Alter Bud Banks

Despite the importance of vegetative reproduction in annual tiller replacement, little is known about the patterns and timing of tiller recruitment from the bud bank, especially regarding fire return intervals and seasons of fire. We examined aboveground plant density, temporal patterns of tiller production, and belowground bud bank dynamics for Bouteloua gracilis (Willd ex. Kunth) Lag. ex Griffiths), Pascopyrum smithii (Rydb.) A. Löve, and Hesperostipa comata (Trin. & Rupr.) Barkworth following summer, fall, and spring prescribed fires at 2-yr, 3-yr, and 6-yr fire return intervals, and their interactions. Fire treatments were initiated in 2006, and buds were assessed July 2011 through July 2013. Density and number of reproductive B. gracilis tillers increased in 2013 following drought during 2012, unlike H. comata, which decreased reproductive tiller production. Irrespective of fire treatments, B. gracilis produced the most buds (8 ? 10 buds ? tiller^? 1) and H. comata produced the least (2 ? 3 buds ? tiller^? 1), with P. smithii producing an intermediate amount (6 ? 8 buds ? tiller^? 1). Immediate B. gracilis and P. smithii bud mortality did not occur for all season and fire return interval treatments. However, H. comata bud mortality increased immediately following summer and fall prescribed fires. Three-yr fire return intervals increased active buds throughout the 2013 winter and growing season for B. gracilis and P. smithii relative to control plots and 2- and 6-yr fire return intervals. Fire stimulated bud activity of B. gracilis and P. smithii relative to nonburned plots. The aboveground and belowground response of H. comata indicated meristem limitations following fire treatments, illustrating greater vulnerability to fire for that species than B. gracilis and P. smithii.     

Fire and Nitrogen Effects on Purple Threeawn (Aristida purpurea) Abundance in Northern Mixed-Grass Prairie Old Fields

Purple threeawn (Aristida purpurea Nutt. varieties) is a native grass capable of increasing on rangelands, forming near monocultures, and creating a stable state. Productive rangelands throughout the Great Plains and Intermountain West have experienced increases in purple threeawn abundance, reducing overall forage quality. Our objectives were to 1) reveal the effects of prescribed fire and nitrogen amendments on purple threeawn abundance and 2) assess nontarget plant response posttreatment. Season of fire (no fire, summer fire, fall fire) and nitrogen addition (0 kg N · ha^?1, 46 kg N · ha^?1, and 80 kg N · ha^?1) were factorially arranged in a completely randomized design and applied to two similar sites in southeastern Montana. We evaluated fire and nitrogen effects on purple threeawn basal cover, relative composition, and current-year biomass one growing season postfire at two sites treated during different years. Spring weather following fire treatments was very different between years and subsequently impacted community response. Initial purple threeawn biomass at both sites was 1 214 ± 46 kg · ha^?1 SEc. When postfire growing conditions were wet, current-year biomass of purple threeawn was reduced 90% and 73% with summer and fall fire, respectively. Under dry postfire growing conditions, purple threeawn current-year biomass was reduced 73% and 58% with summer and fall fire, respectively. Nitrogen additions had no effect on purple threeawn current-year biomass at either site. Current-year biomass of C₃ perennial grass doubled with nitrogen additions and was not impacted by fire during a wet spring. Nitrogen additions and fire had no effect on C₃ perennial grass current-year biomass following a dry spring. Prescribed fire appears to be a highly effective tool for reducing purple threeawn abundance on semiarid rangelands, with limited detrimental impacts to nontarget species.     

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.     

Grazing History Effects on Rangeland Biomass,Cover and Diversity Responses to Fire and Grazing Utilization

Exclusion of large grazers from rangelands that evolved with significant grazing pressure can alter natural processes and may have legacy effects by changing magnitude or direction of community responses to subsequent disturbance. Three moderately grazed pastures were paired with 12-ha areas with 15 yr of livestock exclusion. Six treatments were assigned to each in a 2 x 3 factorial arrangement of fire (fall fire or no fire) and grazing utilization (0%, 50%, or 75% biomass removal) to determine grazing history effects on rangeland response to subsequent disturbance. Livestock exclusion increased C₃ perennial grass (1 232 vs. 980 ± 50 kg ? ha^-1) and forbs (173 vs. 62 ± 19 kg ? ha^-1) and reduced C₄ perennial grass (36 vs. 180 ± 25 kg ? ha^-1) with no effect on total current-year biomass. Diversity was greater in pastures than exclosures (H’ = 1.5400 vs. 1.3823 ± 0.0431). Every biomass, cover, and diversity measure, except subshrub biomass, was affected by fire, grazing utilization, or both. Contrary to expectations, grazing history only interacted with fire effects for old standing dead material and interactions with grazing utilization were limited to old dead, bare ground, richness and dominance. Fire by grazing utilization interaction was limited to bare ground. Fire reduced annual grass (64 vs. 137 ± 29 kg ? ha^-1), forbs (84 vs. 133 ± 29 kg ? ha^-1), and diversity (H’ = 1.3260 vs. 1.5005 ± 0.0537) with no difference in total current-year biomass (1 557 vs. 1 594 ± 66 kg ? ha^-1). Grazing to 75% utilization reduced total current-year biomass (1 467 vs. 1 656 ± 66 kg ? ha^-1) and dominance (0.4824 vs. 0.5584 ± 0.0279). Grazing history affected starting points for most variables, but changes caused by grazing utilization or fire were similar between pastures and exclosures, indicating management decisions can be made based on independent knowledge of grazing or fire effects.     

Interannual Herbaceous Biomass Response to Increasing Honey Mesquite Cover on Two Soils

This study quantified herbaceous biomass responses to increases in honey mesquite (Prosopis glandulosa Torr.) cover on two soils from 1995 to 2001 in north central Texas. Vegetation was sampled randomly with levels of mesquite ranging from 0% to 100%. With no mesquite covering the silt loam soils of bottomland sites, peak herbaceous biomass averaged (±SE) 3 300 ± 210 kg · ha⁻¹ vs. 2 560 ± 190 kg · ha⁻¹ on clay loam soils of upland sites (P = 0.001). A linear decline of 14 ± 2.5 kg · ha⁻¹ in herbaceous biomass occurred for each percent increase in mesquite cover (P = 0.001). The slope of this decline was similar between soils (P = 0.135). Herbaceous biomass with increasing mesquite cover varied between years (P = 0.001) as did the slope of decline (P = 0.001). Warm-season herbaceous biomass decreased linearly with increasing mesquite cover averaging a 73 ± 15% reduction at 100% mesquite cover (P = 0.001) compared to 0% mesquite cover. Cool-season herbaceous biomass was similar between soils with no mesquite, 1 070 ± 144 kg · ha⁻¹ for silt loam vs. 930 ± 140 kg · ha⁻¹ for clay loam soils, but averaged 340 ± 174 kg · ha⁻¹ more on silt loam than on clay loam soils at 100% mesquite cover (P = 0.004). Multiple regression analysis indicated that each centimeter of precipitation received from the previous October through the current September produced herbaceous biomass of 51 kg · ha⁻¹ on silt loam and 41 kg · ha⁻¹ on clay loam soils. Herbaceous biomass decreased proportionally with increasing mesquite cover up to 29 kg · ha⁻¹ at 100% mesquite cover for each centimeter of precipitation received from January through September. Increasing mesquite cover reduces livestock forage productivity and intensifies drought effects by increasing annual herbaceous biomass variability. From a forage production perspective there is little advantage to having mesquite present.     

Effects of 34 Years of Experimentally Manipulated Burn Seasons and Frequencies on Prairie Plant Composition

Historically, tallgrass prairie burns occurred at many seasons and frequencies. Currently, tallgrass prescribed burns often occur annually in the spring, usually for cattle forage production. Altering burning season and frequency is known to affect plant composition and biomass production, but researchers are still uncertain how burning season and frequency interact. We present the long-term effects of a factorial combination of different burn seasons (spring, summer, autumn, or variable [rotated through seasons]) and frequencies (annual or quadrennial) on the plant composition and biomass production of an ungrazed, restored tallgrass prairie in eastern Nebraska, United States. The experimental plots were established in 1978 and visually surveyed for baseline data in 1979 and 1981. Experimental burn treatments were begun in 1982. Plots were visually surveyed until 2011 with the following results: 1) annual spring and summer burns increased C₄ graminoid abundance; 2) annual autumn burns increased forb abundance; 3) burn season had little effect on plant composition for quadrennial burns; and 4) variable season burns generally led to plant composition that was intermediate between annual spring/summer and annual autumn burns. We also clipped biomass to estimate aboveground annual net primary production (ANPP) in 2015, a year in which both annual and quadrennial burns occurred. Total ANPP did not differ significantly between burn frequencies nor between spring and autumn burns (772 g m^? 2 average) but was lower in summer burns (541 g m^? 2). ANPP results were similar to visual surveys, with significantly higher C₄ graminoid ANPP in spring than autumn burns and significantly lower forb and C₃ graminoid ANPP in spring than autumn burns. Overall, these results suggest autumn burns can increase forb and C₃ graminoid abundance, without strongly affecting total ANPP relative to spring burns. Future studies should compare plant and livestock production between spring and autumn burns in grazed fields.     

Plant Community and Soil Environment Response to Summer Fire in the Northern Great Plains

Fire is an important process in many ecosystems, especially grasslands. However, documentation of plant community and soil environment responses to fire is limited for semiarid grasslands relative to that for mesic grasslands. Replicated summer fire research is lacking but necessary because summer is the natural fire season and the period of most wildfires in the western United States. We evaluated summer fire effects on soil temperature, soil moisture, aboveground biomass, root biomass, and functional group composition for 2 yr in semiarid C₃-dominated northern Great Plains. Following pre-treatment measures, four 0.75-ha sites were burned during August for comparison with nonburned sites, and the experiment was repeated the next year on adjacent sites to assess weather effects. Soils were about 0.5°C cooler on burned sites in the first experiment and similar in the second. Burned sites were consistently 1% drier than nonburned sites. Litter was reduced by fire but did not account for changes in soil moisture because differences occurred before the growing season. Current-year aboveground biomass and root biomass were similar between treatments, indicating productivity was resistant to summer fire. Perennial C₃ grasses increased in dominance because of positive biomass responses to fire for all but the bunchgrass, Hesperostipa comata, and a reduction of annual grasses. Perennial C₄ grasses were unaffected by summer fire. H. comata was resilient, with biomass on burned sites equaling nonburned sites the second growing season. Biomass was more responsive to precipitation than fire, and the fire-induced changes in species composition suggest exclusion of fire may be a greater disturbance than summer fire.     

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.     

Fire,Defoliation, and Competing Species Alter Aristida purpurea Biomass,Tiller, and Axillary Bud Production

Aristida purpurea (purple threeawn) is a competitive native perennial grass with monoculturistic tendencies and poor palatability. We examined effects of fire, defoliation, and interspecific/intraspecific planting for 1) threeawn responses in the presence of threeawn, Bouteloua gracilis, or Pascopyrum smithii, and 2) B. gracilis and P. smithii response with threeawn. Biomass, aboveground production, tillers, and axillary buds were analyzed following two fire and four clipping treatments applied to three species–pair combinations in a completely randomized factorial design with nine replications. Fire killed 36% of threeawn. Fire reduced surviving threeawn biomass 61% and reduced production 27%. Threeawn production was greatest when neither plant was clipped and least when competing species were moderately clipped, or when both plants were severely clipped. Tiller counts of burned threeawn were similar among clipping treatments, and less than non-clipped or moderately clipped plants not burned. Fire decreased threeawn axillary buds on average by 25%. Moderately clipped plants had greater production than those from other clipping treatments across species. Average threeawn percentage of pot biomass was greater with B. gracilis (46 ± 3% SE) than P. smithii (38 ± 3% SE). Fire reduced threeawn from 60 ± 3% to 23 ± 3% of pot biomass, indicating good potential for rapid reductions in threeawn dominance and restoration of plant diversity with fire.     

Short-Term Control of an Invasive C4 Grass With Late-Summer Fire

Yellow bluestem (Bothriochloa ischaemum [L.] Keng var. songarica [Rupr. ex Fisch & C.A. Mey] Celarier & Harlan) is a non-native, invasive C₄ grass common in southern Great Plains rangelands. We measured the effects of a single late-summer (September 2006) fire on yellow bluestem at two sites in central Texas (Fort Hood and Onion Creek). At Fort Hood, relative frequency of yellow bluestem in burned plots decreased from 74 ± 4% (preburn; mean ± standard error) to 9 ± 2% (2007) and remained significantly lower compared with unburned plots through 2009 (burned: 14 ± 2%; unburned: 70 ± 14%). At Onion Creek, yellow bluestem initially decreased from 74 ± 5% (2006) to 32 ± 7% (2007). Yellow bluestem recovered substantially by 2009 (67 ± 10%) but was still significantly lower than in unburned transects (96 ± 1%). Relative frequency of other graminoids increased significantly in burned plots (compared with preburn values) at Fort Hood (preburn: 11 ± 4%; 2009: 29 ± 7%) but not at Onion Creek (preburn: 24 ± 6%; 2009: 22 ± 7%). Frequency of forbs increased dramatically in the first growing season after fire (Fort Hood: 15 ± 2% to 76 ± 3%; Onion Creek: 2 ± 2% to 45 ± 5%), then decreased through the third growing season (Fort Hood: 57 ± 6%; Onion Creek: 11 ± 4%). Key differences between the sites include much higher biomass at Fort Hood than at Onion Creek (8 130 kg ? ha^-1 vs. 2 873 kg ? ha^-1), more recent grazing at Onion Creek (ending in 2000 vs. before 1996 at Fort Hood), and higher rainfall after the Onion Creek burn (214 mm in 20 days vs. 14 mm). Late-summer fire can temporarily decrease yellow bluestem frequency, but effects vary with site conditions and precipitation. Restoring dominance by native grasses may require additional management.     

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.     

Restoring Perennial Grasses in Medusahead Habitat: Role of Tilling,Fire, Herbicides,and Seeding Rate

Restoring arid regions degraded by invasive annual grasses to native perennial grasses is a critical conservation goal. Targeting site availability, species availability, and species performance is a key strategy for reducing invasive annual grass cover while simultaneously increasing the abundance of seeded native perennial grasses. However, the potential for establishing successful seedings is still highly variable in rangeland ecosystems, likely because of variable year-to-year weather. In this study, we evaluated the independent and combined inputs of tilling, burning, applying imazapic herbicide, and varying seeding rates on existing species and seeded native perennial grass performance from 2008 to 2012 in a southwestern Idaho rangeland ecosystem. We found that combining tilling, fire, and herbicides produced the lowest annual grass cover. The combination of fire and herbicides yielded the highest seeded species density in the hydrologic year (HY) (October ? September) 2010, especially at higher than minimum recommended seeding rates. Although the independent and combined effects of fire and herbicides directly affected the growth of resident species, they failed to affect seeded species cover except in HY 2010, when weather was favorable for seedling growth. Specifically, low winter temperature variability (few freeze-thaw cycles) followed by high growing season precipitation in HY 2010 yielded 14 × more seeded perennial grasses than any other seeding year, even though total annual precipitation amounts did not greatly vary between 2009 and 2012. Collectively, these findings suggest that tilling, applying prescribed fire, and herbicides before seeding at least 5 × the minimum recommended seeding rate should directly reduce resident annual grass abundance and likely yield high densities of seeded species in annual grass ? dominated ecosystems, but only during years of stable winter conditions followed by wet springs.     

Forb Cover Increases After Solarization and Winter Fire in a Grassland Invaded by Yellow Bluestem

Solarization (covering soil and vegetation with plastic) has long been used in agriculture to control undesirable plants, but solarization of invasive plants in rangelands has shown mixed and species-specific results. Yellow bluestem (Bothriochloa ischaemum (L.) Keng var. songarica (Rupr. ex Fisch & C.A. Mey) Celarier & Harlan), an invasive perennial C₄ grass, is common throughout the southern Great Plains and is not controlled by winter prescribed fire. We tested whether solarization (tarping) with black plastic, combined with winter prescribed fire, could control yellow bluestem. We applied three treatments (with four replicates): solarization (August to November 2017) + fire (January 2018), trimming + fire, and fire only. Results after two growing seasons show that total yellow bluestem cover in solarized + fire plots was reduced to 54% ± 10% (mean ± standard error), lower than trimmed + fire (82% ± 5%, p < 0.01) and fire only plots (78% ± 6%, p = 0.01). Forb cover in solarized + fire plots (15% ± 4%) was much higher than trimmed + fire (4% ± 1%, p < 0.01) and fire only plots (3% ± 1%, p < 0.01). Native forb richness was only slightly higher in solarized + fire plots (16 ± 2 species) compared to fire only (10 ± 2 species, p = 0.08) and trimmed + fire plots (10 ± 1 species, p = 0.08). Interestingly, native forb richness in all plots increased compared to pre-treatment values (2 ± 1 species for all treatments, p < 0.01). Solarization + winter fire can slightly decrease yellow bluestem cover and greatly increase native forb cover, creating islands of diversity in otherwise low-diversity grasslands. However, repeated treatments or alternative techniques will be needed for full control of yellow bluestem.     

Plant Community Responses to Mastication and Mulching of One-Seed Juniper (Juniperus monosperma)

Mechanical cutting and mastication of juniper trees aims to restore grassland habitat by reducing the density of encroaching woody species. However, the associated soil disturbance may also create conduits for invasive species, a risk that must be mitigated by land managers. We characterized herbaceous communities in treated and adjacent untreated areas in a piñon-juniper (Pinus edulis and Juniper monosperma) woodland in northern Arizona 2.5 years after treatment. Untreated plots had 4 × the herbaceous cover (82%) than treated plots (21%). Within treated plots, native species cover (19%) was 10 × higher than invasive species cover (2%). Furthermore, treated plots exhibited greater plant community variability and diversity than untreated plots, driven by an increase in the diversity of native grasses and non-native forbs. No new recruits were Arizona listed noxious weeds, indicating that, at least in the short term, mastication is not producing invasive species hot spots in this piñon-juniper woodland.     

Can Mowing Substitute for Fire in Semiarid Grassland?

Accumulating data indicate the importance of fire in rangeland systems. Mowing is a common management technique sometimes considered a surrogate for fire. However, direct comparisons of fire and mowing effects are limited. Our objective was to determine whether mowing can substitute for fire in rangeland by comparing effects on plant biomass, composition, cover, soil nutrients, and forage quality. Three disturbance treatments (nontreated control, spring mowing with clipping removal, and spring fire) were randomly assigned to 21 plots (5 × 5 m) each on silty and claypan ecological sites in a completely randomized design, with seven replications per site. Current-yr biomass was similar among control, mowed, and burned treatments (1 003, 974, 1 022 ± 64 kg ● ha^− 1). Mowing shifted functional group composition by reducing C₃ perennial grass 12% and increasing forbs 8%. Non-native species were a larger component of mowed (12%) than control (6%) or burned plots (4%). Fire increased bare ground 35%, reduced litter 32%, and eliminated previous yrs’ growth the first growing season. Plant-available soil N and S more than doubled with fire, and there was a trend for more P in burned plots. Mowing effects were limited to a trend for less soil Fe. Mowing affected 42% of the forage quality variables with a 2% average improvement across all variables. Fire affected 84% of the variables, with a 12% average improvement. Mowing increased forage P and K, whereas fire increased forage concentrations of N, K, P, S, Mg, Fe, Mn, and Cu. Total digestible nutrients increased 1.1% with mowing and 2.1% with fire. In vitro dry matter disappearance increased 2.2% with mowing and 6.7% with fire. Burned plots had greater in vitro fermentation than controls or mowed plots. Although mowing can be a useful management tool, it is not a substitute for the ecological effects of rangeland fire.     

Evaluation of Herbicide and Disking to Control Invasive Bluestems in a South Texas Coastal Prairie

Conservation and restoration efforts of native grasslands are being hindered by invasive, exotic plants. Exotic bluestem grasses (Bothriochloa and Dichanthium spp.) have become increasingly invasive throughout the rangelands of the central and southern Great Plains, United States. Accordingly, the aim of this study was to evaluate the efficacy of glyphosate, imazapyr, and imazapyr + glyphosate treatments with or without disking to remove exotic bluestems from a south Texas coastal prairie. We evaluated three different control regimens: 1) herbicide treatments only, 2) herbicide treatments followed by two diskings (H + D), and 3) disking followed by herbicide treatments (D + H). Percent exotic bluestem, native grass, and forb cover were visually estimated at 0 (pre-treatment: May 2006), 20, 52, and 104 wk after treatment (WAT). The herbicide-only and H + D regimens were ineffective at controlling exotic bluestems. However, exotic bluestem cover in herbicide-treated plots of the D + H regimen was significantly lower (P ≤ 0.05) compared to control plots and most treatment plots of the herbicide-only and H + D regimens up to 52 WAT. Control regimens did not notably facilitate an increase in native grass cover from pre-treatment levels, but native grass cover remained the highest, and increased the most, in some imazapyr-treated plots of the herbicide-only and D + H regimens, respectively. In the H + D and D + H regimens, disking resulted in a flush of forb cover (up to 50%) at 52 WAT; yet forb cover was ≤ 5% in these plots by 104 WAT. Exotic bluestem cover recovered back to, or was greater than, pre-treatment levels among most treatment plots across all three control regimens at 104 WAT. This study suggests that follow-up control measures are needed to suppress the re-invasion of exotic bluestems after initial control efforts. Additional studies are needed to evaluate other strategies to control exotic bluestems in rangelands of the central and southern United States.     

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.     

Targeted Grazing for Native Forbs in Annual Grasslands

Targeted grazing is a promising strategy for addressing management issues in annual grasslands. We evaluated targeted cattle grazing strategies for tarweed (Hemizonia fitchii A. Gray) and vinegarweed (Trichostema lanceolatum Benth.). These native annual forbs provide biodiversity to annual grass-dominated landscapes, in addition to being important pollinator plants that discourage yellow starthistle (Centaurea solstitialis L.) invasion. However, these forbs can form dense stands that interfere with grazing. Therefore, we sought grazing strategies that promote sparse stands to maintain livestock production while supporting other ecosystem services. Treatments were 1) early grazing when dominant annual grasses were vegetative, 2) late grazing when grasses were senescing, 3) repeated grazing, and 4) a nongrazed control. These treatments were applied in 2011, 2012, and 2013. In 2012, neither tarweed nor vinegarweed were observed regardless of treatment, likely due to low water availability during their major growth period. In 2011 and 2013, grazing grasses repeatedly throughout the growing season increased tarweed to 3 ? 5 plants m^? 2, compared with < 1 plants m^? 2 in the control, and in 2011 repeated grazing also increased vinegarweed. Therefore, although environmental factors can prevent tarweed and vinegarweed from forming stands some years, defoliating grasses repeatedly from vegetative through senesced stages is the most reliable way to encourage these forbs in annual grasslands. However, a single period of defoliation can also encourage tarweed: In 2011 and 2013, we found a single period of grazing as annual grasses senesced and tarweed began rapid growth increased tarweed, possibly by increasing light availability. Finally, we found grazing once early in the growing season provided low tarweed and vinegarweed densities, likely because the long postgrazing period allowed annual grasses to recover and competitively suppress these forbs. Therefore, early grazing may reduce/prevent overly dense tarweed and vinegarweed stands.