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Ecological site R028BY053NV
DROUGHTY CALCAREOUS LOAM 8-10 P.Z.(Burned Site)
Accessed: 09/14/2026
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Draft. A draft ecological site description is either incomplete or has not undergone quality control and quality assurance review.
MLRA notes
Major Land Resource Area (MLRA): 028B–Central Nevada Basin and Range
MLRA 28B occurs entirely in Nevada and comprises about 23,555 square miles (61,035 square kilometers). More than nine-tenths of this MLRA is federally owned. This area is in the Great Basin Section of the Basin and Range Province of the Intermontane Plateaus. It is an area of nearly level, aggraded desert basins and valleys between a series of mountain ranges trending north to south. The basins are bordered by long, gently sloping to strongly sloping alluvial fans. The mountains are uplifted fault blocks with steep sideslopes. Many of the valleys are closed basins containing sinks or playas. Elevation ranges from 4,900 to 6,550 feet (1,495 to 1,995 meters) in the valleys and basins and from 6,550 to 11,900 feet (1,995 to 3,630 meters) in the mountains.
The mountains in the southern half are dominated by andesite and basalt rocks that were formed in the Miocene and Oligocene. Paleozoic and older carbonate rocks are prominent in the mountains to the north. Scattered outcrops of older Tertiary intrusives and very young tuffaceous sediments are throughout this area. The valleys consist mostly of alluvial fill, but lake deposits are at the lowest elevations in the closed basins. The alluvial valley fill consists of cobbles, gravel, and coarse sand near the mountains in the apex of the alluvial fans. Sands, silts, and clays are on the distal ends of the fans.
The average annual precipitation ranges from 4 to 12 inches (100 to 305 millimeters) in most areas on the valley floors. Average annual precipitation in the mountains ranges from 8 to 36 inches (205 to 915 millimeters) depending on elevation. The driest period is from midsummer to midautumn. The average annual temperature is 34 to 52 degrees F (1 to 11 degrees C). The freeze-free period averages 125 days and ranges from 80 to 170 days, decreasing in length with elevation.
The dominant soil orders in this MLRA are Aridisols, Entisols, and Mollisols. The soils in the area dominantly have a mesic soil temperature regime, an aridic or xeric soil moisture regime, and mixed or carbonatic mineralogy. They generally are well drained, loamy or loamyskeletal, and shallow to very deep.
Nevada’s climate is predominantly arid, with large daily ranges of temperature, infrequent severe storms and heavy snowfall in the higher mountains. Three basic geographical factors largely influence Nevada’s climate: continentality, latitude, and elevation. The strong continental effect is expressed in the form of both dryness and large temperature variations. Nevada lies on the eastern, lee side of the Sierra Nevada Range, a massive mountain barrier that markedly influences the climate of the State. The prevailing winds are from the west, and as the warm moist air from the Pacific Ocean ascend the western slopes of the Sierra Range, the air cools, condensation occurs and most of the moisture falls as precipitation. As the air descends the eastern slope, it is warmed by compression, and very little precipitation occurs. The effects of this mountain barrier are felt not only in the West but throughout the state, as a result the lowlands of Nevada are largely desert or steppes.
The temperature regime is also affected by the blocking of the inland-moving maritime air. Nevada sheltered from maritime winds, has a continental climate with well-developed seasons and the terrain responds quickly to changes in solar heating. Nevada lies within the midlatitude belt of prevailing westerly winds which occur most of the year. These winds bring frequent changes in weather during the late fall, winter and spring months, when most of the precipitation occurs.
To the south of the mid-latitude westerlies, lies a zone of high pressure in subtropical latitudes, with a center over the Pacific Ocean. In the summer, this high-pressure belt shifts northward over the latitudes of Nevada, blocking storms from the ocean. The resulting weather is mostly clear and dry during the summer and early fall, with occasional thundershowers. The eastern portion of the state receives noteworthy summer thunderstorms generated from monsoonal moisture pushed up from the Gulf of California, known as the North American monsoon. The monsoon system peaks in August and by October the monsoon high over the Western U.S. begins to weaken and the precipitation retreats southward towards the tropics (NOAA 2004).
Ecological site concept
This site occurs on summits and sideslopes of fan piedmonts, and on footslopes of hills. Slopes range from 4 to 30 percent, but slope gradients of 4 to 15 percent are most typical. Elevations are 5800 to 6300 feet.
The climate associated with this site is semiarid, characterized by cool, moist winters and warm, dry summers. Average annual precipitation is 5 to 8 inches. Mean annual air temperature is 45 to 50 degrees F. The average growing season is about 100 to 120 days.
The soils associated with this site are generally moderately deep to deep and well drained. They are moderately coarse with surface textures being gravelly to very gravelly. They have medium runoff and moderate to moderately rapid permeability. Available water holding capacity is low.
The reference state is dominated by spiny hopsage, black sagebrush, Indian ricegrass and needleandthread. Production ranges from 200 to 600 pounds per acre.
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Table 1. Dominant plant species
Tree Not specified
Shrub (1) Grayia spinosa
(2) Artemisia novaHerbaceous (1) Achnatherum hymenoides
Physiographic features
This site occurs on summits and sideslopes of fan piedmonts, and on footslopes of hills. Slopes range from 4 to 30 percent, but slope gradients of 4 to 15 percent are most typical. Elevations are 5800 to 6300 feet.
Table 2. Representative physiographic features
Landforms (1) Hill
Climatic features
The climate associated with this site is semiarid, characterized by cool, moist winters and warm, dry summers.
Average annual precipitation ranges from 7 to 10 inches. Mean annual air temperature is about 45 to 50 degrees F. The average growing season is about 100 to 120 days.
Mean annual precipitaion at the MONTELLO 1 SE,NEVADA climate station (265352) is 6.95 inches. Monthly mean precipitation is:
January 0.61; February 0.46; March 0.43; April 0.61;
May 0.91; June 0.83; July 0.56; August 0.52;
September 0.51; October 0.51;
November 0.53; December 0.48.Table 3 Representative climatic features
Frost-free period (average) 110 days Freeze-free period (average) 110 days Precipitation total (average) 10 in BarLineFigure 1. Monthly precipitation range
BarLineFigure 2. Monthly average minimum and maximum temperature
Figure 3. Annual precipitation pattern
Figure 4 Annual average temperature pattern
">Influencing water features
This are no influencing water features associated with this site.
Soil features
The soils associated with this site are shallow to a duripan and well drained. They are moderately coarse with surface textures being gravelly to very gravelly. They have medium runoff and moderate to moderately rapid permeability. Available water holding capacity is low.
The representative soil series is Eastwell, a Loamy-skeletal, mixed, superactive, mesic, shallow Xereptic Haplodurids. Diagnostic horizons include an Ochric epipedon from the soil surface to 18 cm, Durinodes from 25 to 38 cm, and a Duripan from 38 to 43 cm. Clay content in the particle control section averages 10 to 27 percent. Rock fragments range from 35 to 50 percent, mainly gravel. Reaction is Moderately alkaline or strongly alkaline. Effervescence is moderately alkaline or violently effervescent. Lithology consists of mixed rock.Table 4. Representative soil features
Surface texture (1) Gravelly loam
Family particle size (1) Loamy
Drainage class Well drained Permeability class Moderate Soil depth 15 – 17 in Surface fragment cover <=3" 20 – 25 % Surface fragment cover >3" Not specified Calcium carbonate equivalent
(0-40in)15 – 30 % Electrical conductivity
(0-40in)Not specified Sodium adsorption ratio
(0-40in)Not specified Soil reaction (1:1 water)
(0-40in)8.4 – 8.8 Subsurface fragment volume <=3"
(Depth not specified)35 – 50 % Subsurface fragment volume >3"
(Depth not specified)Not specified Ecological dynamics
An ecological site is the product of all the environmental factors responsible for its development and it has a set of key characteristics that influence a site’s resilience to disturbance and resistance to invasives. Key characteristics include 1) climate (precipitation, temperature), 2) topography (aspect, slope, elevation, and landform), 3) hydrology (infiltration, runoff), 4) soils (depth, texture, structure, organic matter), 5) plant communities (functional groups, productivity), and 6) natural disturbance regime (fire, herbivory, etc.) (Caudle et al. 2013). Biotic factors that that influence resilience include site productivity, species composition and structure, and population regulation and regeneration (Chambers et al. 2013).
Periodic drought regularly influences sagebrush ecosystems and drought duration and severity has increased throughout the 20th century in much of the Intermountain West. Major shifts away from historical precipitation patterns have the greatest potential to alter ecosystem function and productivity. Species composition and productivity can be altered by the timing of precipitation and water availability within the soil profile (Bates et al. 2006).
Native insect outbreaks are also important drivers of ecosystem dynamics in sagebrush communities. Climate is generally believed to influence the timing of insect outbreaks especially a sagebrush defoliator, Aroga moth (Aroga websteri). Aroga moth infestations have occurred in the Great Basin in the 1960s, early 1970s, and is ongoing in Nevada since 2004 (Bentz et al. 2008). Thousands of acres of sagebrush have been impacted, with partial to complete die-off observed (Gates 1964, Hall 1965), but the research is inconclusive of the damage sustained by black sagebrush populations.
Black sagebrush is generally long-lived; therefore it is not necessary for new individuals to recruit every year for perpetuation of the stand. Infrequent large recruitment events and simultaneous low, continuous recruitment is the foundation of population maintenance (Noy-Meir 1973). Survival of the seedlings is dependent on adequate moisture conditions.
The perennial bunchgrasses that are co-dominant with the shrubs include Indian ricegrass and needleandthread. Sandberg’s bluegrass and squirreltail are other important grass species. These species generally have somewhat shallower root systems than the shrubs, but root densities are often as high or higher than those of shrubs in the upper 0.5 m of the soil profile. General differences in root depth distributions between grasses and shrubs results in resource partitioning in these shrub/grass systems.
The Great Basin sagebrush communities have high spatial and temporal variability in precipitation both among years and within growing seasons. Nutrient availability is typically low but increases with elevation and closely follows moisture availability. The invasibility of plant communities is often linked to resource availability. Disturbance can decrease resource uptake due to damage or mortality of the native species and depressed competition or can increase resource pools by the decomposition of dead plant material following disturbance. The invasion of sagebrush communities by cheatgrass has been linked to disturbances (fire, abusive grazing) that have resulted in fluctuations in resources (Chambers et al. 2007).
The range and density of Utah juniper has increased since the middle of the nineteenth century (Tausch 1999, Miller and Tausch 2000). Causes for expansion of Utah juniper into sagebrush ecosystems include wildfire suppression, historic livestock grazing, and climate change (Bunting 1994). Mean fire return intervals prior to European settlement in black sagebrush ecosystems were greater than 100 years, however frequent enough to inhibit the encroachment of Utah juniper into these low productive sagebrush cover types (Kitchen and McArthur 2007). Thus, trees were isolated to fire-safe areas such as rocky outcroppings and areas with low-productivity. An increase in crown density causes a decrease in understory perennial vegetation and an increase in bare ground. This allows for the invasion of non-native annual species such as cheatgrass. With annual species in the understory wildfire can become more frequent and increase in intensity. With frequent wildfires these plant communities can convert to annual species with a sprouting shrub and juvenile tree overstory.
This ecological site has low to moderate resilience to disturbance and resistance to invasion. Increased resilience increases with elevation, aspect, increased precipitation and increased nutrient availability. Six possible stable states have been identified for this site.
Fire Ecology:
Fire is not a major disturbance of these community types (Winward 2001), and would be infrequent. Historic fire return intervals have been estimated at 100-200 years (Kitchen and McArthur 2007); however, fires were probably patchy and very infrequent due to the low productivity of these sites. Black sagebrush plants have no morphological adaptations for surviving fire and must reestablish from seed following fire (Wright et al. 1979). The ability of black sagebrush to establish after fire is mostly dependent on the amount of seed deposited in the seed bank the year before the fire. Seeds typically do not persist in the soil for more than 1 growing season (Beetle 1960). A few seeds may remain viable in soil for 2 years (Meyer 2008); however, even in dry storage, black sagebrush seed viability has been found to drop rapidly over time, from 81% to 1% viability after 2 and 10 years of storage, respectively (Stevens et al. 1981). Thus, repeated frequent fires can eliminate black sagebrush from a site, however black sagebrush in zones receiving 12 to 16 inches of annual precipitation have been found to have greater fire survival (Boltz 1994). In lower precipitation zones, spiny hopsage and/or shadscale may become the dominant shrub species following fire. Douglas’ rabbitbrush and ephedra can also sprout after fire and become a dominant shrub on this site often with an understory of Sandberg’s bluegrass and/or cheatgrass and other weedy species.
The effect of fire on bunchgrasses relates to culm density, culm-leaf morphology, and the size of the plant. The initial condition of bunchgrasses within the site along with seasonality and intensity of the fire all factor into the individual species response. The two dominant grasses on this site, Indian ricegrass and needleandthread grass, have different responses to fire. Needleandthread is top-killed by fire but is likely to resprout if fire does not consume above ground stems (Akinsoji 1988, Bradley, Noste and Fischer 1992). In a study by Wright and Klemmedson (1965), season of burn rather than fire intensity seemed to be the crucial factor in mortality for needleandthread grass. Early spring season burning was seen to kill the plants while August burning had no effect. Indian ricegrass is fairly fire tolerant (Wright 1985), which is likely due to its low culm density and below ground plant crowns. Indian ricegrass has been found to reestablish on burned sites through seed dispersed from adjacent unburned areas (Young 1983, West 1994). Thus the presence of surviving, seed producing plants is necessary for reestablishment of Indian ricegrass. Grazing management following fire to promote seed production and establishment of seedlings is important.
Sandberg’s bluegrass, a minor component of this ecological site, has been found to increase following fire likely due to its low stature and productivity (Daubenmire 1975). Sandberg’s bluegrass may retard reestablishment of deeper rooted bunchgrass. Repeated frequent fire in this community will eliminate both black sagebrush and Indian ricegrass from the site and facilitate the establishment of an annual weed community with varying amounts of Sandberg’s bluegrass, spiny hopsage and rabbitbrush.
Utah juniper is usually killed by fire, and is most vulnerable to fire when it is under four feet tall (Bradley et al. 1992). Larger trees, because they have foliage farther from the ground and thicker bark, can survive low severity fires but mortality does occur when 60% or more of the crown is scorched (Bradley et al. 1992). With the low production of the understory vegetation, high severity fires within this plant community were not likely and rarely became crown fires (Bradley et al. 1992, Miller and Tausch 2000). Tree density on this site increases with grazing management that favors the removal of fine fuels and management focused on fire suppression. With an increase of cheatgrass in the understory, fire severity is likely to increase. Utah juniper reestablishes by seed from nearby seed source or surviving seeds. Utah juniper begins to produce seed at about 30 years old (Bradley et al. 1992). Seeds establish best through the use of a nurse plant such as sagebrush and rabbitbrush (Everett and Ward 1984, Tausch and West 1988, Bradley et al. 1992). Utah juniper woodlands reach mature stage between 85 to 150 years after fire (Barney and Frischknecht 1974, Tausch and West 1988).State and transition model
More interactive model formats are also available. View Interactive Models
Click on state and transition labels to scroll to the respective textEcosystem states
State 1 submodel, plant communities
State 2 submodel, plant communities
State 3 submodel, plant communities
State 1
Reference StateThe Reference State is a representative of the natural range of variability under pristine conditions. The Reference State has three general community phases; a shrub-grass dominant phase, and a shrub dominant phase and a grass dominate phase. State dynamics are maintained by interactions between climatic patterns and disturbance regimes. Negative feedbacks enhance ecosystem resilience and contribute to the stability of the state. These include the presence of all structural and functional groups, low fine fuel loads, and retention of organic matter and nutrients. Plant community phase changes are primarily driven by fire, periodic drought and/or insect or disease attack. Due to the nature and extent of disturbance in this site, all three plant community phases would likely occur in a mosaic across the landscape. Utah juniper may be present on the site, but will only occur as scattered trees and will not dominate the site.
Community 1.1
Community PhaseThis plant community is dominated by black sagebrush in the overstory with Indian ricegrass and needleandthread grass dominant in the understory. Utah juniper may be present. Potential vegetative composition is about 40% grasses, 5% forbs and 55% shrubs. Approximate ground cover (basal and crown) is 25 to 35 percent.
Figure 5. Annual production by plant type (representative values) or group (midpoint values)
Table 5. Annual production by plant type
Plant type Low
(lb/acre)Representative value
(lb/acre)High
(lb/acre)Shrub/Vine 110 220 330 Grass/Grasslike 80 160 240 Forb 10 20 30 Total 200 400 600 Community 1.2
Community PhaseThis community phase is characteristic of a post-disturbance, early seral community phase. Indian ricegrass and needleandthread will increase and dominate the community. Sprouting shrubs such as Douglas’ rabbitbrush, spiny hopsage, and shadscale may increase. Black sagebrush could still be present in unburned patches. Forbs may increase post-fire but will likely return to pre-burn levels within a few years.
Community 1.3
Community PhaseBlack sagebrush increases in the absence of disturbance. Decadent sagebrush dominates the overstory and the deep-rooted perennial bunchgrasses in the understory are reduced, either from competition with shrubs or from herbivory. Sandberg’s bluegrass will likely increase in the understory and may be the dominant grass on the site. Scattered Utah juniper trees may be present on the site.
Pathway a
Community 1.1 to 1.2A low severity fire would decrease the overstory of sagebrush and allow for the understory perennial grasses to increase. Fires are typically low severity resulting in a mosaic pattern due to low fuel loads. A fire following an unusually wet spring facilitating an increase in fine fuels may be more severe and reduce sagebrush cover to trace amounts.
Pathway b
Community 1.1 to 1.3Absence of disturbance over time, significant herbivory, chronic drought or combinations of these would allow the sagebrush overstory to increase and dominate the site. This will generally cause a reduction in perennial bunch grasses; however Sandberg’s bluegrass may increase in the understory depending on the timing and intensity of herbivory. Heavy spring utilization will favor an increase in sagebrush.
Pathway a
Community 1.2 to 1.1Time and lack of disturbance will allow sagebrush to establish.
Pathway a
Community 1.3 to 1.1A low severity fire, herbivory or combinations will reduce the sagebrush overstory and create a sagebrush/grass mosaic.
Pathway b
Community 1.3 to 1.2Fire will decrease or eliminate the overstory of sagebrush and allow for the perennial bunchgrasses to dominate the site. Fires will typically be high intensity due to the dominance of sagebrush resulting in removal of the overstory shrub community.
State 2
Current Potential StateThis state is similar to the Reference State 1.0 and has three similar community phases. Ecological function has not changed in this state, but the resiliency of the state has been reduced by the presence of invasive weeds. These non-native species can be highly flammable, and promote fire where historically fire had been infrequent. Negative feedbacks enhance ecosystem resilience and contribute to the stability of the state. These include the presence of all structural and functional groups, low fine fuel loads and retention of organic matter and nutrients. Positive feedbacks decrease ecosystem resilience and stability of the state. These include the non-natives high seed output, persistent seed bank, rapid growth rate, ability to cross pollinate and adaptations for seed dispersal.
Community 2.1
Community PhaseThis community phase is compositionally similar to the Reference State Community Phase 1.1 with the presence non-native species in trace amounts. This community is dominated by black sagebrush in the overstory with Indian ricegrass and needleandthread grass dominant in the understory. Utah juniper may be present.
Community 2.2
Community PhaseThis community phase is characteristic of a post-disturbance, early seral community where annual non-native species are present. Sagebrush is present in trace amounts; perennial bunchgrasses dominate the site. Depending on fire severity patches of intact sagebrush may remain. Rabbitbrush or other sprouting shrubs may be increasing. Shadscale may increase. Annual non-native species generally respond well after fire and may be stable or increasing within the community.
Community 2.3
Community Phase (At Risk)Black sagebrush dominates the overstory and perennial bunchgrasses in the understory are reduced, either from competition with shrubs or from inappropriate grazing, or from both. Rabbitbrush may be a significant component. Sandberg’s bluegrass will likely increase in the understory and may be co-dominant with the deep rooted bunchgrasses. Utah juniper may be present and without management will likely increase. Annual non-native species are stable or increasing. This community is at risk of crossing a threshold to either State 3.0 (grazing or fire) or State 4.0 (fire).
Pathway a
Community 2.1 to 2.2A low severity fire would decrease the overstory of sagebrush and allow for the understory perennial grasses to increase. Fires are typically low severity resulting in a mosaic pattern due to low fuel loads. A fire following an unusually wet spring or a change in management favoring an increase in fine fuels may be more severe and reduce sagebrush cover to trace amounts. Annual non-native species are likely to increase after fire.
Pathway b
Community 2.1 to 2.3Absence of disturbance over time, chronic drought, inappropriate grazing management or combinations of these would allow the sagebrush overstory to increase and dominate the site. Inappropriate grazing management reduces the perennial bunchgrass understory; conversely Sandberg bluegrass may increase in the understory.
Pathway a
Community 2.2 to 2.1Absence of disturbance over time and/or grazing management that favors the establishment and growth of sagebrush allows the shrub component to recover. The establishment of black sagebrush can take many years.
Pathway a
Community 2.3 to 2.1Grazing management that reduces shrubs will allow for the perennial bunchgrasses in the understory to increase. Heavy late-fall/winter grazing may cause mechanical damage to sagebrush promoting the perennial bunchgrass understory. Brush treatments with minimal soil disturbance will also decrease sagebrush and release the perennial understory. Annual non-native species are present and may increase in the community. A low severity fire would decrease the overstory of sagebrush and allow for the understory perennial grasses to increase. Due to low fuel loads in this State, fires will likely be small creating a mosaic pattern.
Pathway b
Community 2.3 to 2.2Fire will decrease or eliminate the overstory of sagebrush and allow for the perennial bunchgrasses to dominate the site. Fires will typically be high intensity due to the dominance of sagebrush resulting in removal of the overstory shrub community. Annual non-native species respond well to fire and may increase post-burn.
State 3
Shrub StateThis state has one community phase is characterized by black sagebrush or a sprouting shrub overstory with a Sandberg’s bluegrass understory. The site has crossed a biotic threshold and site processes are being controlled by shrubs. Bare ground has increased and pedestalling of grasses may be excessive.
Community 3.1
Community PhaseBlack sagebrush dominates overstory while Sandberg’s bluegrass dominates the understory. Deep-rooted perennial bunchgrasses have significantly declined. Annual non-native species may be present. Bare ground and soil redistribution may be increasing. If present on the site, Utah juniper is increasing. The community phase may be at risk of transitioning into a Tree State or Annual State
Community 3.2
Community Phase (At Risk)Shadscale or rabbitbrush dominate the overstory. Broom snakeweed may be present to increasing. Annual non-native species may be increasing and bare ground is significant. This site is at risk for an increase in invasive annual weeds.
Pathway a
Community 3.1 to 3.2Fire reduces black sagebrush to trace amounts and allows for sprouting shrubs such as rabbitbrush to dominate. Shadscale may also establish post-fire and become dominate. Inappropriate or excessive sheep grazing could also reduce cover of sagebrush and allow for shadscale or sprouting shrubs to dominate the community. Brush treatments with minimal soil disturbance would facilitate sprouting shrubs and Sandberg’s bluegrass.
Transition A
State 1 to 2Trigger: Introduction of non-native annual plants. Slow variables: Over time the annual non-native plants will increase within the community. Threshold: Any amount of introduced non-native species causes an immediate decrease in the resilience of the site. Annual non-native species cannot be easily removed from the system and have the potential to significantly alter disturbance regimes from their historic range of variation.
Transition A
State 2 to 3Trigger: To Community Phase 3.1: Inappropriate cattle/horse grazing will decrease or eliminate deep rooted perennial bunchgrasses, increase Sandberg bluegrass and favor shrub growth and establishment. To Community Phase 3.2: Severe fire will remove sagebrush overstory, decrease perennial bunchgrasses and enhance Sandberg’s bluegrass. Soil disturbing brush treatments and/or inappropriate sheep grazing will reduce sagebrush and potentially increase sprouting shrubs and Sandberg’s bluegrass. Slow variables: Long term decrease in deep-rooted perennial grass density and/or black sagebrush. Threshold: Loss of deep-rooted perennial bunchgrasses changes nutrient cycling, nutrient redistribution, and reduces soil organic matter. Loss of long-lived, black sagebrush changes the temporal and depending on the replacement shrub, the spatial distribution of nutrient cycling.
Additional community tables
Table 6. Community 1.1 plant community composition
Group Common name Symbol Scientific name Annual production () Foliar cover (%) Grass/Grasslike1 Primary Perennial Grasses 88–160 Indian ricegrass ACHY Achnatherum hymenoides 60–100 – needle and thread HECO26 Hesperostipa comata 20–40 – bluegrass POA Poa 8–20 – 2 Secondary Perennial Grasses 20–40 squirreltail ELEL5 Elymus elymoides 2–12 – Forb3 Perennial 16–52 globemallow SPHAE Sphaeralcea 8–20 – cryptantha CRYPT Cryptantha 2–8 – spiny phlox PHHO Phlox hoodii 2–8 – Shrub/Vine4 Primary Shrubs 140–220 spiny hopsage GRSP Grayia spinosa 80–120 – black sagebrush ARNO4 Artemisia nova 60–100 – 5 Secondary Shrubs 20–40 yellow rabbitbrush CHVI8 Chrysothamnus viscidiflorus 4–20 – Nevada jointfir EPNE Ephedra nevadensis 4–20 – bud sagebrush PIDE4 Picrothamnus desertorum 4–20 – Table 7. Community 1.2 plant community composition
Group Common name Symbol Scientific name Annual production () Foliar cover (%) Table 8. Community 1.3 plant community composition
Group Common name Symbol Scientific name Annual production () Foliar cover (%) Table 9. Community 2.1 plant community composition
Group Common name Symbol Scientific name Annual production () Foliar cover (%) Table 10. Community 2.2 plant community composition
Group Common name Symbol Scientific name Annual production () Foliar cover (%) Table 11. Community 2.3 plant community composition
Group Common name Symbol Scientific name Annual production () Foliar cover (%) Table 12. Community 3.1 plant community composition
Group Common name Symbol Scientific name Annual production () Foliar cover (%) Table 13. Community 3.2 plant community composition
Group Common name Symbol Scientific name Annual production () Foliar cover (%) Interpretations
Animal community
Livestock/Wildlife Grazing Interpretations:
Black sagebrush palatability has been rated as moderate to high depending on the ungulate and the season of use (Horton 1989, Wambolt 1996). The palatability of black sagebrush increases the potential negative impacts on remaining black sagebrush plants from grazing or browsing pressure following fire (Wambolt 1996). Pronghorn utilize black sagebrush heavily (Beale and Smith 1970). On the Desert Experiment Range, black sagebrush was found to comprise 68% of pronghorn diet even though it was only the 3rd most common plant. Fawns were found to prefer black sagebrush utilizing it more than all other forage species combined (Beale and Smith 1970). Domestic livestock will also utilize black sagebrush. The domestic sheep industry that emerged in the Great Basin in the early 1900s was largely based on wintering domestic sheep in black sagebrush communities (Mozingo 1987). Domestic sheep will browse black sagebrush during all seasons of the year depending on the availability of other forage species, with greater amounts being consumed in fall and winter. Black sagebrush is generally less palatable to cattle than to domestic sheep and wild ungulates (McArthur et al. 1979); however, cattle use of black sagebrush has also been shown to be greatest in fall and winter (Schultz and McAdoo 2002), with only trace amounts being consumed in summer (Van Vuren 1984).
Inappropriate grazing management during the growing season will cause a decline in understory plants such as needleandthread and Indian ricegrass. Growing season grazing by cattle may initially cause a decrease in the bunchgrass component and give a competitive advantage to shrub species including black sagebrush (Eckert et al. 1972).
Indian ricegrass is a deep-rooted, cool season perennial bunchgrass that is adapted primarily to sandy soils. Indian ricegrass is a preferred forage species for livestock and wildlife (Cook 1962, Booth et al. 2006). This species is often heavily utilized in winter because it cures well (Booth et al. 2006). It is also readily utilized in early spring, being a source of green feed before most other perennial grasses have produced new growth (Quinones 1981). Booth et al. (2006) note that the plant does well when utilized in winter and spring. Cook and Child (1971), however, found that repeated heavy grazing reduced crown cover, which may reduce seed production, density, and basal area of these plants. Additionally, heavy early spring grazing reduces plant vigor and stand density (Stubbendieck et al. 1985). In eastern Idaho, productivity of Indian ricegrass was at least 10 times greater in undisturbed plots than in heavily grazed ones (Pearson 1976). Cook and Child (1971) found significant reduction in plant cover after 7 years of rest from heavy (90%) and moderate (60%) spring use. The seed crop may be reduced where grazing is heavy (Bich et al. 1995). Tolerance to grazing increases after May, thus spring deferment may be necessary for stand enhancement (Pearson 1964, Cook and Child 1971); however, utilization of less than 60% is recommended.
Needle-and-thread grass is most commonly found on warm/dry soils (Miller et al. 2013). It is not grazing tolerant and will be one of the first grasses to decrease under heavy grazing pressure (Smoliak et al. 1972, Tueller and Blackburn 1974). Heavy grazing is likely to reduce basal area of these plants (Smoliak et al. 1972). With the reduction in competition from deep rooted perennial bunchgrasses, shallower rooted grasses such as Sandberg bluegrass and forbs may increase (Smoliak et al. 1972). Further degradation of the grass community can lead to an invasion by exotic annual species such as halogeton and cheatgrass.
Reduced bunchgrass vigor or density provides an opportunity for Sandberg’s bluegrass expansion and/or cheatgrass and other invasive species to occupy interspaces, leading to increased fire frequency and potentially an annual plant community. Sandberg’s bluegrass increases under grazing pressure (Tisdale and Hironaka 1981) and is capable of co-existing with cheatgrass. Excessive sheep grazing favors Sandberg’s bluegrass; however, where cattle are the dominant grazers, cheatgrass often dominates (Daubenmire 1970). Thus, depending on the season of use, the type of grazing animal, and site conditions, either Sandberg’s bluegrass or cheatgrass may become the dominant understory with inappropriate grazing management.
Halogeton is a non-competitive plant that tends to invade areas that are susceptible to repeated disturbance such as; livestock trails, roadsides, trampled areas near watering holes or corrals and rangeland areas stripped of the natural vegetation by excessive grazing or other soil disturbing activities (Young 2002). It was first introduced into the western U.S. during the 20th century with the first collection being made near Wells, Nevada in 1934. Halogeton is highly toxic to sheep and has been responsible for thousands of sheep deaths throughout the western U.S., which triggered a massive effort to eradicate the introduced species (Young 2002).
Halogeton has two distinct seed forms; black form which consists of the achene only and brown form which consists of the achene and attached sepals (Tisdale and Zappetini 1953, Robocker et al. 1969). The black form of halogeton seed germinate readily under a wide range of pH and salt concentrations within the first year. The brown form of seed was found to be 100 percent viable at the end of 2 years and 15 percent viable at the end of 10 years, proving that halogeton seed may remain viable in the soil for up to 10 years (Robocker et al. 1969). Eradication of this species is problematic therefore appropriate range management practices focused on soil and rangeland integrity may keep the plant in check.
Recreational uses
Aesthetic value is derived from the diverse floral and faunal composition and the colorful flowering of wild flowers and shrubs during the spring and early summer. This site offers rewarding opportunities to photographers and for nature study. This site is used for camping and hiking and has potential for upland and big game hunting.
Other products
Some Native American peoples traditionally ground parched seeds of spiny hopsage to make pinole flour. Indian ricegrass was traditionally eaten by some Native Americans. The Paiutes used the seed as a reserve food source.
Other information
Spiny hopsage has moderate potential for erosion control and low to high potential for long-term revegetation projects. It can improve forage, control wind erosion, and increase soil stability on gentle to moderate slopes. Spiny hopsage is suitable for highway plantings on dry sites in Nevada. Black sagebrush is an excellent species to establish on sites where management objectives include restoration or improvement of domestic sheep, pronghorn, or mule deer winter range. Needleandthread is useful for stabilizing eroded or degraded sites.
Supporting information
Type locality
Location 1: Elko County, NV Township/Range/Section T27N R65E S17 Latitude 40° 13′ 4″ Longitude 114° 39′ 51″ General legal description About 13 miles southeast of Currie along footslopes of Currie Hills, Goshute Lake area, Elko County, Nevada. This site also occurs in White Pine County, Nevada. Other references
Akinsoji, A. 1988. Postfire vegetation dynamics in a sagebrush steppe in southeastern Idaho, USA. Vegetatio 78:151-155.
Beale, D.M. and A.D. Smith. 1970. Forage use, water consumption, and productivity of pronghorn antelope in western Utah. Journal of Wildlife Management 34(3):570-582
Beetle, A.A. 1960. A study of sagebrush: The section Tridentatae of Artemisia. Bulletin 368. Laramie, WY: University of Wyoming, Agricultural Experiment Station. 83 p.
Bentz, B., D. Alston, and T. Evans. 2008. Great Basin Insect Outbreaks. Pages 45-48 in Collaborative Management and Research in the Great Basin -- Examining the issues and developing a framework for action Gen. Tech. Rep. RMRS-GTR-204. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fort Collins, CO.
Bich, B.S., J.L. Butler, and C.A. Schmidt. 1995. Effects of differential livestock use of key plant species and rodent populations within selected Oryzopsis hymenoides/Hilaria jamesii communities in Glen Canyon National Recreation Area. The Southwestern Naturalist 40(3):281-287.
Blaisdell, J. P., and J. F. Pechanec. 1949. Effects of Herbage Removal at Various Dates on Vigor of Bluebunch Wheatgrass and Arrowleaf Balsamroot. Ecology 30:298-305.
Booth, D. T., C. G. Howard, and C. E. Mowry. 2006. 'Nezpar'Indian ricegrass: description, justification for release, and recommendations for use. Rangelands Archives 2:53-54.
Bradley, A. F., N. V. Noste, and W. C. Fischer. 1992. Gen. Tech. Rep. INT-287: Fire ecology of forests and woodlands in Utah. . U.S. Department of Agriculture, Forest Service, Intermountain Research Station, Ogden, UT.
Britton, C. M., G. R. McPherson, and F. A. Sneva. 1990. Effects of burning and clipping on five bunchgrasses in eastern Oregon. Great Basin Naturalist 50:115-120.
Boltz, M. 1994. Factors influencing postfire sagebrush regeneration in south-central Idaho. In: Monsen, S.B. and S.G. Kitchen (compilers). Proceedings--ecology and management of annual rangelands; 1992 May 18-22; Boise, ID. Gen. Tech. Rep. INT-GTR-313. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Research Station: Pgs 281-290.
Bradley, A., Noste, N. and Fischer, W. 1992. Fire ecology of forests and woodlands in Utah. USDA Forest Service, Intermountain Research Station, General Technical Report INT-287, 92 pp.
Britton, C. M., G. R. McPherson, and F. A. Sneva. 1990. Effects of burning and clipping on five bunchgrasses in eastern Oregon. Great Basin Naturalist 50:115-120.
Bunting, S. 1994. Effects of Fire on Juniper woodland ecosystems in the great basin.in Proceedings--Ecology and Management of Annual Rangelands. USDA: FS Intermountain Research Station.
Busso, C. A., and J. H. Richards. 1995. Drought and clipping effects on tiller demography andgrowth of two tussock grasses in Utah. Journal of Arid Environments 29:239-251.
Chambers, J., B. Bradley, C. Brown, C. D’Antonio, M. Germino, J. Grace, S. Hardegree, R. Miller, and D. Pyke. 2013. Resilience to Stress and Disturbance, and Resistance to Bromus tectorum L. Invasion in Cold Desert Shrublands of Western North America. Ecosystems:1-16.
Chambers, J. C., B. A. Roundy, R. R. Blank, S. E. Meyer, and A. Whittaker. 2007. What makes great basin sagebrush ecosystems invasible by Bromus tectorum? Ecological Monographs 77:117-145.
Cook, C. W. 1962. An Evaluation of Some Common Factors Affecting Utilization of Desert Range Species. Journal of Range Management 15:333-338.
Cook, C.W. and R.D. Child. 1971. Recovery of desert plants in various states of vigor. Journal of
Range Management 24(5):339-343.
Daubenmire, R.F. 1970. Steppe vegetation of Washington. Technical Bulletin 62. Pullman, WA:
Washington State University, College of Agriculture, Washington Agricultural Experiment Station. 131 p.
Daubenmire, R.F. 1975. Plant succession on abandoned fields, and fire influences, in a steppe area in southeastern Washington. Northwest Science 49(1):36-48.
Eckert, R.E., Jr., A.D. Bruner and G.J. Klomp. 1972. Response of understory species following herbicidal control of low sagebrush. Journal of Range Management 25:280-285.
Eckert, R.E., Jr. and J.S. Spencer. 1987. Growth and reproduction of grasses heavily grazed under rest-rotation management. Journal of Range Management 40(2):156-159.
Evans, R.A. and J.A. Young. 1978. Effectiveness of rehabilitation practices following wildfire in a degraded big sagebrush-downy brome community. Journal of Range Management 31(3):185-188.
Everett, R. L. and K. Ward. 1984. Early plant succession on pinyon-juniper controlled burns. Northwest Science 58:57-68.
Fire Effects Information System (Online; http://www.fs.fed.us/database/feis/plants/).
Ganskopp, D. 1988. Defoliation of Thurber needlegrass: herbage and root responses. Journal of Range Management 41(6):472-476.
Gates, D. H. 1964. Sagebrush infested by leaf defoliating moth. Journal of Range Management 17:209-210.
Hall, R. C. 1965. Sagebrush defoliator outbreak in Northern California. Res. Note PSW-RN-075., Berkeley, CA.
Horton, H. 1989. Interagency forage and conservation planting guide for Utah. Extension Circular 433. Logan, UT: Utah State University, Cooperative Extension Service. 67 p.
Hurd, R. M., and C. K. Pearse. 1944. Relative Palatability of Eight Grasses used in Range Reseeding. Agronomy Journal 36:162-165.
Houghton, J.G., C.M. Sakamoto, and R.O. Gifford. 1975. Nevada's Weather and Climate, Special Publication 2. Nevada Bureau of Mines and Geology, Mackay School of Mines, University of Nevada, Reno, NV.
Jones, T. A., M. H. Ralphs, and D. C. Nielson. 1994. Cattle Preference for 4 Wheatgrass Taxa. Journal of Range Management 47:119-122.
Kitchen, S.G. and E.D. McArthur. 2007. Big and black sagebrush landscapes. In: Hood, S.M. and M. Miller (eds.). Fire ecology and management of the major ecosystems of southern Utah. Gen. Tech. Rep. RMRS-GTR-202. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station: 73-95.
Koniak, S. 1985. Succession in pinyon-juniper woodlands following wildfire in the Great Basin. The Great Basin Naturalist 45:556-566.
Martens, E., D. Palmquist, and J.A. Young. 1994. Temperature profiles for germination of cheatgrass versus native perennial bunchgrasses. In: Monsen, S.B. and S.G. Kitchen (compilers). Proceedings--ecology and management of annual rangelands; 1992 May 18-22; Boise, ID. Gen. Tech. Rep. INT-GTR-313. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Research Station:238-243.
McArthur, E.D., A.C. Blauer, A.P. Plummer, and R. Stevens. 1979. Characteristics and hybridization of important Intermountain shrubs. III. Sunflower family. Res. Pap. INT-220. Ogden, UT. U.S. Department of Agriculture, Forest Service, Intermountain Forest and Range Experiment Station. 82 p.
Meyer, S.E. 2008. Artemisia L.--sagebrush. In: Bonner, F.T. and R.P. Karrfalt (eds.). The woody plant seed manual. Agriculture Handbook 727. Washington, DC: U.S. Department of Agriculture, Forest Service: 274-280.
Miller, R. F., J. C. Chambers, D. A. Pyke, F. B. Pierson, and C. J. Williams. 2013. A review of fire effects on vegetation and soils in the Great Basin Region: response and ecological site characteristics.
Miller, R. F. and R. J. Tausch. 2000. The role of fire in pinyon and juniper woodlands: a descriptive analysis. Pages 15-30 in Proceedings of the invasive species workshop: the role of fire in the control and spread of invasive species. Fire conference.
Mozingo, H.N. 1987. Shrubs of the Great Basin: A natural history. Reno, NV: University of Nevada Press. 342 p.
Mueggler, W. F. 1975. Rate and Pattern of Vigor Recovery in Idaho Fescue and Bluebunch Wheatgrass. Journal of Range Management 28:198-204.
National Oceanic and Atmospheric Administration. 2004. The North American Monsoon. Reports to the Nation. National Weather Service, Climate Prediction Center. Available online: http://www.weather.gov/
Pearson, L.C. 1976. Primary production in grazed and ungrazed desert communities of eastern
Idaho. Ecology 46(3):278-285.
Quinones, F.A. 1981. Indian ricegrass evaluation and breeding. Bulletin 681. Las Cruces, NM:
New Mexico State University, Agricultural Experiment Station. 19 p.
Robocker, W. C., M. C. Williams, R. A. Evans, and P. J. Torell. 1969. Effects of Age, Burial, and Region on Germination and Viability of Halogeton Seed. Weed Science 17:63-65.
Schultz, B. and K. McAdoo. 2002. Common sagebrush in Nevada. Special Publication SP-02-02. Reno, NV. University of Nevada, Cooperative Extension. 9 p.
Smoliak, S., J. F. Dormaar, and A. Johnston. 1972. Long-Term Grazing Effects on Stipa-Bouteloua Prairie Soils. Journal of Range Management 25:246-250.
Stevens, R., K.R. Jorgensen, and J.N. Davis. 1981. Viability of seed from thirty-two shrub and forb species through fifteen years of warehouse storage. The Great Basin Naturalist 41(3):274-277.
Stubbendieck, J., J.T. Nichols, and K.K. Roberts. 1985. Nebraska range and pasture grasses(including grass-like plants). E.C. 85-170. Lincoln, NE: University of Nebraska, Department of Agriculture, Cooperative Extension Service. 75 p.
Tausch, R. J. 1999. Historic pinyon and juniper woodland development. Proceedings: ecology and management of pinyon–juniper communities within the Interior West. Ogden, UT, USA: US Department of Agriculture, Forest Service, Rocky Mountain Research Station, RMRS-P-9:12-19.
Tausch, R. J. and N. E. West. 1988. Differential establishment of pinyon and juniper following fire. American Midland Naturalist:174-184.
Tisdale, E. W. and G. Zappetini. 1953. Halogeton Studies on Idaho Ranges. Journal of Range Management 6:225-236.
Tisdale, E.W. and M. Hironaka. 1981. The sagebrush-grass region: a review of the ecological literature. Bull. 33. Moscow, ID: University of Idaho, Forest, Wildlife and Range Experiment Station. 31 p.
Tueller, P. T. and W. H. Blackburn. 1974. Condition and Trend of the Big Sagebrush/Needleandthread Habitat Type in Nevada. Journal of Range Management 27:36-40.
Uresk, D.W., J.F. Cline, and W.H. Rickard. 1976. Impact of wildfire on three perennial grasses in south-central Washington. Journal of Range Management 29(4):309-310.
USDA-NRCS Plants Database (Online; http://www.plants.usda.gov).
Van Vuren, D. 1984. Summer diets of bison and cattle in southern Utah. Journal of Range Management 37(3): 260-261.
Wambolt, C.L. 1996. Mule deer and elk foraging preference for 4 sagebrush taxa. Journal of Range Management 49(6):499-503.
Winward, A.H. 2001. Sagebrush taxonomy and ecology workshop--October 5-6, 1999. In: Vegetation, wildlife and fish ecology and rare species management--Wasatch-Cache National Forest. Logan, UT: U.S. Department of Agriculture, Forest Service, Intermountain Region, Uinta- Wasatch-Cache National Forest.
Wright, H. A. 1985. Effects of fire on grasses and forbs in sagebrush-grass communities. Pages 12-21 in Rangeland Fire Effects; A Symposium: Boise, ID, USDI-BLM.
Wright, H.A., L.F. Neuenschwander, and C.M. Britton. 1979. The role and use of fire in sagebrush-grass and pinyon-juniper plant communities: A state-of-the-art review. Gen. Tech. Rep. INT-58. Ogden, UT. U.S. Department of Agriculture, Forest Service, Intermountain Forest and Range Experiment Station. 48 p.
Wright, H. A., and J. O. Klemmedson. 1965. Effect of Fire on Bunchgrasses of the Sagebrush-Grass Region in Southern Idaho. Ecology 46:680-688.
Wright, H. A. 1985. Effects of fire on grasses and forbs in sagebrush-grass communities. Pages 12-21 in Rangeland Fire Effects; A Symposium: Boise, ID, USDI-BLM.
Young, R.P. 1983. Fire as a vegetation management tool in rangelands of the Intermountain region. In: Monsen, S.B. and N. Shaw (eds). Managing Intermountain rangelands—improvement of range and wildlife habitats: Proceedings of symposia; 1981 September 15-17; Twin Falls, ID; 1982 June 22-24; Elko, NV. Gen. Tech. Rep. INT-157. Ogden, UT. U.S. Department of Agriculture, Forest Service, Intermountain Forest and Range Experiment Station. Pgs 18-31.
Young, J. A. 2002. Halogeton Grazing Management: Historical Perspective. Journal of Range Management 55:309-311.
Fire Effects Information System (Online; http://www.fs.fed.us/database/feis/plants/).
USDA-NRCS Plants Database (Online; http://www.plants.usda.gov).
Houghton, J.G., C.M. Sakamoto, and R.O. Gifford. 1975. Nevada’s Weather and Climate, Special Publication 2. Nevada Bureau of Mines and Geology, Mackay School of Mines, University of Nevada, Reno, NV.
National Oceanic and Atmospheric Administration. 2004. The North American Monsoon. Reports to the Nation. National Weather Service, Climate Prediction Center. Available online: http://www.weather.gov/
Contributors
MD
T.Stringham/P.Novak-EcheniqueRangeland health reference sheet
Interpreting Indicators of Rangeland Health is a qualitative assessment protocol used to determine ecosystem condition based on benchmark characteristics described in the Reference Sheet. A suite of 17 (or more) indicators are typically considered in an assessment. The ecological site(s) representative of an assessment location must be known prior to applying the protocol and must be verified based on soils and climate. Current plant community cannot be used to identify the ecological site.
Author(s)/participant(s) Contact for lead author Date Approved by Approval date Composition (Indicators 10 and 12) based on Annual Production Indicators
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Number and extent of rills:
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Presence of water flow patterns:
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Number and height of erosional pedestals or terracettes:
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Bare ground from Ecological Site Description or other studies (rock, litter, lichen, moss, plant canopy are not bare ground):
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Number of gullies and erosion associated with gullies:
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Extent of wind scoured, blowouts and/or depositional areas:
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Amount of litter movement (describe size and distance expected to travel):
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Soil surface (top few mm) resistance to erosion (stability values are averages - most sites will show a range of values):
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Soil surface structure and SOM content (include type of structure and A-horizon color and thickness):
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Effect of community phase composition (relative proportion of different functional groups) and spatial distribution on infiltration and runoff:
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Presence and thickness of compaction layer (usually none; describe soil profile features which may be mistaken for compaction on this site):
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Functional/Structural Groups (list in order of descending dominance by above-ground annual-production or live foliar cover using symbols: >>, >, = to indicate much greater than, greater than, and equal to):
Dominant:
Sub-dominant:
Other:
Additional:
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Amount of plant mortality and decadence (include which functional groups are expected to show mortality or decadence):
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Average percent litter cover (%) and depth ( in):
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Expected annual annual-production (this is TOTAL above-ground annual-production, not just forage annual-production):
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Potential invasive (including noxious) species (native and non-native). List species which BOTH characterize degraded states and have the potential to become a dominant or co-dominant species on the ecological site if their future establishment and growth is not actively controlled by management interventions. Species that become dominant for only one to several years (e.g., short-term response to drought or wildfire) are not invasive plants. Note that unlike other indicators, we are describing what is NOT expected in the reference state for the ecological site:
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Perennial plant reproductive capability:
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