Natural Resources
Conservation Service
Ecological site R028BY026NV
FRACTURED STONY LOAM 14+ P.Z.
Accessed: 04/19/2024
General information
Provisional. A provisional ecological site description has undergone quality control and quality assurance review. It contains a working state and transition model and enough information to identify the ecological site.
Figure 1. Mapped extent
Areas shown in blue indicate the maximum mapped extent of this ecological site. Other ecological sites likely occur within the highlighted areas. It is also possible for this ecological site to occur outside of highlighted areas if detailed soil survey has not been completed or recently updated.
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
Following field visits (2012) and a comprehensive review of ecological site concepts and soil map unit components (2016) it has been determined this ecological site concept cannot be separated from 028BY015NV based on soil characteristics, abiotic factors or response to disturbance. There is limited data available for this concept and it is of limited extent.
For the purposes of the provisional ecological site initiative, Fractured Stony Loam 14+"PZ, 028BY026NV, should be considered an obsolete concept. Please refer to the soil features section for information on how individual existing occurrences of this site will be handled. A review of ecological literature supports this decision. Please refer to the ecological dynamic for a discussion on disturbance return interval and sprouting shrub species in the sagebrush ecosystem.
Associated sites
| R025XY004NV |
LOAMY SLOPE 16+ P.Z. |
|---|---|
| R028BY015NV |
LOAMY SLOPE 12-16 P.Z. |
| R028BY030NV |
LOAMY 12-16 P.Z. |
| R028BY035NV |
GRAVELLY CLAYPAN 14+ P.Z. |
| R028BY036NV |
CLAYPAN 14+ P.Z. |
| R028BY038NV |
MOUNTAIN RIDGE 14+ P.Z. |
| R028BY046NV |
GRAVELLY LOAM 12-14 P.Z. |
Similar sites
| R028BY046NV |
GRAVELLY LOAM 12-14 P.Z. PUTR2 dominant shrub |
|---|---|
| R028BY035NV |
GRAVELLY CLAYPAN 14+ P.Z. PUTR2-ARAR8 codominant shrubs |
| R028BY091NV |
GRAVELLY CALCAREOUS LOAM 14+ P.Z. burned phase ACTH7 and/or ACOCO absent |
Table 1. Dominant plant species
| Tree |
Not specified |
|---|---|
| Shrub |
(1) Amelanchier utahensis |
| Herbaceous |
(1) Pseudoroegneria spicata subsp. spicata |
Physiographic features
This site occurs on convex mountain sideslopes. Slopes range from 8 to 75 percent, but slope gradients of 15 to 50 percent are most typical. Elevations are 6500 to 8500 feet.
Table 2. Representative physiographic features
| Landforms |
(1)
Mountain slope
|
|---|---|
| Flooding frequency | None |
| Ponding frequency | None |
| Elevation | 6,500 – 8,500 ft |
| Slope | 15 – 50% |
Climatic features
The climate associated with this site is semiarid, characterized by cold, moist winters and warm, dry summers.
The average annual precipitation ranges from 10 to 16 inches. Mean annual air temperature is about 45 to 50 degrees F. The average growing season is 100 to 120 days.
Mean annual precipitation across the range in which this ES occurs is 11.9 inches: Jan. 0.99; Feb. 1.05; Mar. 1.15; Apr. 1.37; May 1.3; Jun. 0.95; Jul. 0.78; Aug. 0.86; Sept. 0.80; Oct. 0.96; Nov. 0.8; Dec. 0.92.
Table 3. Representative climatic features
| Frost-free period (average) | 100 days |
|---|---|
| Freeze-free period (average) | 120 days |
| Precipitation total (average) | 12 in |
Figure 2. Monthly precipitation range
Figure 3. Monthly average minimum and maximum temperature
Figure 4. Annual precipitation pattern
Figure 5. Annual average temperature pattern
Climate stations used
-
(1) EUREKA [USC00262708], Eureka, NV
-
(2) RUTH [USC00267175], Ely, NV
Influencing water features
Influencing water features are not associated with this site.
Soil features
The soils associated with this site are very deep, well drained and formed in residuum/colluvium derived from mixed volcanic rocks. These soils are characterized by a mollic epipedon, an argillic horizon and greater than 35 percent rock fragments.
Following a review of ecological site concepts and soil map unit components it has been determined this ecological site concept cannot be separated from 028BY015NV based on soil characteristics or abiotic factors. Fractured Stony Loam 14+" PZ, 028BY026NV, should be considered an obsolete concept. Acres of McIvey will be correlated to Loamy slope 12-16", 028BY015NV. Acres of Lithic Argixerolls will be correlated to Gravely Clay 12-14" PZ, 028BY087NV. Acres of Birchcreek will be correlated as appropriate. Future work will determine if the plant community represented by this site will be added to State 1 of the 028BY015NV STM.
Table 4. Representative soil features
| Parent material |
(1)
Residuum
–
quartzite
|
|---|---|
| Surface texture |
(1) Gravelly loam (2) Gravelly loam |
| Family particle size |
(1) Clayey |
| Drainage class | Well drained |
| Permeability class | Moderately slow |
| Soil depth | 40 – 60 in |
| Surface fragment cover <=3" | 20 – 30% |
| Surface fragment cover >3" | 5% |
| Available water capacity (0-40in) |
3 – 5 in |
| Calcium carbonate equivalent (0-40in) |
Not specified |
| Electrical conductivity (0-40in) |
Not specified |
| Sodium adsorption ratio (0-40in) |
Not specified |
| Soil reaction (1:1 water) (0-40in) |
6.3 – 6.8 |
| Subsurface fragment volume <=3" (Depth not specified) |
15 – 20% |
| Subsurface fragment volume >3" (Depth not specified) |
35 – 60% |
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 invasion. 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 influence resilience include site productivity, species composition and structure, and population regulation and regeneration (Chambers et al 2013).
The reference plant community for Fractured Stony Loam 14+, 028BY026NV is dominated by Utah serviceberry (Amelanchier utahensis). This ecological site concept is not well documented and is of limited extent. At this time there are no species composition differences, abiotic factors or soil characteristics that separate this site from the mountain big sagebrush dominated concept Loamy Slope 12-16”, 028BY015NV. Utah serviceberry is found in a wide range of habitat types across the western US and into the Rocky Mountains. It is possible Fractured Stony Loam 14+, 028BY026NV, is a community phase of a Loamy Slope 12-16", 028BY015NV. In the future additional data will be collected to determine if the plant community represented by this site will be included in State 1 of the 028BY015NV STM. A cursory review of the literature supports this decision. It is well documented that Utah serviceberry is an early seral species, it is known to be fire tolerant and shade intolerant (Zlatnik 1999).
The ecological site is dominated by deep-rooted cool season, perennial bunchgrasses and long-lived shrubs (50+ years) with high root to shoot ratios. The dominant shrubs usually root to the full depth of the winter-spring soil moisture recharge, which ranges from 1.0 and over 3.0 m. (Comstock and Ehleringer 1992). Root length of mature sagebrush plants was measured to a depth of two meters in alluvial soils in Utah (Richards and Caldwell 1987). Tap roots of antelope bitterbrush have been documented from 4.5 to 5.4 m in length (McConnell 1961). These shrubs have a flexible generalized root system with development of both deep taproots and laterals near the surface (Comstock and Ehleringer 1992).
Mountain big sagebrush and antelope bitterbrush are 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 bluebunch wheatgrass, western and Thurber needlegrass, and bluegrass. These species generally have somewhat shallower root systems than the shrubs, but root densities are often as high as or higher than those of shrubs in the upper 0.5 m but taper off more rapidly than shrubs. Differences in root depth distributions between grasses and shrubs result 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 moisture resource supporting the greatest amount of plant growth is usually the water stored in the soil profile during the winter. 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 uptake 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). Dobrowolski et al. (1990) cite multiple authors on the extent of the soil profile exploited by the competitive exotic annual cheatgrass. Specifically, the depth of rooting is dependent on the size the plant achieves and in competitive environments cheatgrass roots were found to penetrate only 15 cm whereas isolated plants and pure stands were found to root at least 1 m in depth with some plants rooting as deep as 1.5 to 1.7 m.
The introduction of annual weedy species, like cheatgrass, may cause an increase in fire frequency and eventually lead to an annual state. Conversely, as fire frequency decreases, sagebrush will increase and with inappropriate grazing management the perennial bunchgrasses and forbs may be reduced.
The ecological site has moderate to high resilience to disturbance and resistance to invasion. Increased resilience increases with elevation, aspect, increased precipitation and increased nutrient availability. Long-term disturbance response may be influenced by small differences in landscape topography. Concave areas receive run-in from adjacent landscapes and consequently retain more moisture to support the growth of deep-rooted perennial grasses (i.e. bluebunch wheatgrass, Thurber needlegrass) whereas convex areas where runoff occurs are slightly less resilient and may have more shallow-rooted perennial grasses (i.e. squirreltail and muttongrass). North slopes are also more resilient than south slopes because lower soil surface temperatures operate to keep moisture content higher on northern exposures. Six possible alternative stable states have been identified for this site.
Fire Ecology:
Fire is believed to be the dominant disturbance force in natural big sagebrush communities. Several authors suggest pre-settlement fire return intervals in mountain big sagebrush communities varied from 15 to 25 years (Burkhardt and Tisdale 1969, Houston 1973, and Miller et al. 2000). Kitchen and McArthur (2007) suggest a mean fire return interval of 40 to 80 years for mountain big sagebrush communities. The range from 15 to 80 years is probably more accurate and reflects the differences in elevation and precipitation where mountain big sagebrush communities occur. On a landscape scale, multiple seral stages were represented in a mosaic reflecting periodic reoccurrence of fire and other disturbances (Crawford et al 2004). Post-fire hydrologic recovery and resilience is primarily influenced by pre-fire site conditions, fire severity, and post-fire weather and land use that relate to vegetation recovery. Fire adaptation by herbaceous species is generally superior to the dominant shrubs, which are typically killed by fire. Sites with low abundances of native perennial grasses and forbs typically have reduced resiliency following disturbance and are less resistant to invasion or increases in cheatgrass (Miller et al 2013).
Mountain big sagebrush is killed by fire (Neunschwander 1980, Blaisdell et al. 1982) and does not resprout (Blaisdell 1953). Post-fire regeneration occurs from seed and will vary depending on site characteristics, seed source, and fire characteristics. Once established mountain big sagebrush seedlings can grow rapidly and may reach reproductive maturity within 3 to 5 years (Bunting et al. 1987). Mountain big sagebrush may return to pre-burn density and cover within 15-20 years following fire, but establishment after severe fires may proceed more slowly (Bunting et al. 1987). Lack of adequate moisture conditions may also slow regeneration.
Utah serviceberry is able to sprout from the root crown following fire and rapidly increases in cover post-fire (Zlatnik 1999). In a fire case study that took place 16 miles northwest of Ely, Nevada, Zschaechner (1985), reported Utah serviceberry plants sprouted following both August and October burns. However, heavy litter accumulation did increase the chance of fire-caused mortality.
Antelope bitterbrush is moderately fire tolerant (McConnell and Smith 1977). It regenerates by seed and resprouting (Blaisdell and Mueggler 1956, McArthur et al. 1982), however sprouting ability is highly variable and has been attributed to genetics, plant age, phenology, soil moisture and texture and fire severity (Blaisdell and Mueggler 1956, Blaisdell et al. 1982, Clark et al. 1982, Cook et al. 1994). Bitterbrush sprouts from a region on the stem approximately 1.5 inches above and below the soil surface; the plant rarely sprouts if the root crown is killed by fire (Blaisdell and Mueggler 1956). Low intensity fires may allow for bitterbrush to sprout; however, community response also depends on soil moisture levels at time of fire (Murray 1983). Lower soil moisture allows more charring of the stem below ground level (Blaisdell and Mueggler 1956), thus sprouting will usually be more successful after a spring fire than after a fire in summer or fall (Murray 1983, Busse et al. 2000, Kerns et al. 2006). If cheatgrass is present, bitterbrush seedling success is much lower. The factor that most limits establishment of bitterbrush seedlings is competition for water resources with the invasive species cheatgrass (Clements and Young 2002).
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. For most forbs and grasses the growing points are located at or below the soil surface providing relative protection from disturbances which decrease above ground biomass, such as grazing or fire. Thus, fire mortality is more correlated to duration and intensity of heat which is related to culm density, culm-leaf morphology, size of plant and abundance of old growth (Young 1983, Wright 1971). Fire will remove aboveground biomass from bluebunch wheatgrass but plant mortality is generally low (Robberecht and Defosse 1995). However, season and severity of the fire will influence plant response. Plant response will vary depending on post-fire soil moisture availability. Thurber needlegrass is moderately resistant to wildfire (Smith and Busby 1981), but can be severely damaged and have high mortality depending on season and severity of fire. Post-fire regeneration usually occurs from seed, but plants that are not completely killed by fire will continue growth during favorable conditions (Koniak 1985).
State and transition model
Figure 6. State and Transition Model
Figure 7. Legend
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Click on state and transition labels to scroll to the respective text
State 1 submodel, plant communities
State 2 submodel, plant communities
State 3 submodel, plant communities
State 4 submodel, plant communities
State 5 submodel, plant communities
State 1
Reference State
The Reference State 1.0 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, a perennial grass dominant phase and a shrub dominant 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.
Community 1.1
Community Phase
The plant community is dominated by Utah serviceberry, bluebunch wheatgrass, and Thurber's needlegrass. Utah serviceberry dominates the visual aspect. Potential vegetative composition is about 35% grasses, 10% forbs and 55% shrubs. Approximate ground cover (basal and crown) is 35 to 45 percent.
Figure 8. 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 | 385 | 495 | 660 |
| Grass/Grasslike | 245 | 315 | 420 |
| Forb | 70 | 90 | 120 |
| Total | 700 | 900 | 1200 |
Community 1.2
Community Phase
This community phase is characteristic of a post-disturbance, early to mid-seral community phase. Bluebunch wheatgrass, Thurber’s needlegrass and other perennial grasses dominate. Mountain big sagebrush cover and production is greatly reduced.
Community 1.3
Community Phase
Mountain big sagebrush increases in the absence of disturbance or with grazing management that favors shrubs. Decadent sagebrush dominates the overstory and the deep-rooted perennial bunchgrasses in the understory are reduced either from competition with shrubs or from grazing management. Utah juniper and/or singleleaf pinyon may be present.
Pathway a
Community 1.1 to 1.2
Fire would reduce or eliminate mountain big sagebrush and allow for perennial bunchgrasses to dominate the site. Fires will typically be small and patchy due to low fuel loads. A fire following an unusually wet spring or a change in management may be more severe and reduce sagebrush to trace amounts. Coupled with drought conditions, a severe infestation of Aroga moth could also reduce in sagebrush within the community, giving a competitive advantage to the perennial grasses and forbs. This phenomenon is more likely at the lower end of the precipitation range.
Pathway b
Community 1.1 to 1.3
Chronic drought may reduce fire frequency and increase shrub cover, time and/or inappropriate grazing management may also favor an increase in Mountain big sagebrush over deep-rooted perennial bunchgrasses. Combinations of these would allow the sagebrush overstory to increase and dominate the site, causing a reduction in the perennial bunchgrasses. Sandberg bluegrass may increase in density depending on the grazing management.
Pathway a
Community 1.2 to 1.1
Time and lack of fire allows for sagebrush to reestablish.
Pathway a
Community 1.3 to 1.1
A low severity fire will reduce the sagebrush overstory and create a sagebrush/grass mosaic. Coupled with drought, an aroga moth infestation may reduce sagebrush dominance and allow recovery of the perennial bunchgrass understory.
Pathway b
Community 1.3 to 1.2
Fire will decrease or eliminate the overstory of sagebrush and allow for the perennial bunchgrasses to dominate the site. Fires will typically be low severity, resulting in a mosaic pattern due to low fine 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. A severe infestation of Aroga moth could also cause a large decrease in sagebrush within the community, giving a competitive advantage to the perennial grasses and forbs.
State 2
Current Potential State
This state is similar to the Reference State 1.0. with similar community phases plus the 2.4 at-risk community phase. Ecological function has not changed, however the resiliency of the state has been reduced by the presence of invasive weeds. 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. Additionally, the presence of highly flammable, non-native species reduces state resilience because these species can promote fire where historically fire has been infrequent leading to positive feedbacks that further the degradation of the system.
Community 2.1
Community Phase
This community phase is similar to the Reference State Community Phase 1.1, with the presence of non-native species in trace amounts. Mountain big sagebrush and bluebunch wheatgrass dominate the site. Thurber’s needlegrass and basin wildrye may be significant components while Sandberg bluegrass and forbs make up smaller percentages by weight of the understory.
Community 2.2
Community Phase
This 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. Mountain big sagebrush decreases, bluebunch wheatgrass, Thurber’s needlegrass, basin wildrye, and other perennial grasses dominate. Bitterbrush, snowberry, and/or rabbitbrush may dominate the overstory aspect for a number of years following fire. Perennial forbs may be a significant component for several years following fire. Annual non-native species are stable or increasing within the community.
Community 2.3
Community Phase (at risk)
Figure 9. Fractured Stony Loam 14” (R028BY026NV) T. Stringham June 2012
This community is at risk of crossing a threshold to another state. Sagebrush dominates the overstory and perennial bunchgrasses in the understory are reduced from competition with shrubs, inappropriate grazing, or both. Rabbitbrush may be a significant component. Sandberg bluegrass may increase and become co-dominate with deep rooted bunchgrasses. Utah juniper and singleleaf pinyon may be present and without management will likely increase. Annual non-natives species may be stable or increasing due to lack of competition with perennial bunchgrasses. This site is susceptible to further degradation from grazing, drought, and fire.
Community 2.4
Community Phase (at risk)
This community is at risk of crossing into an annual state. Native bunchgrasses dominate; however, annual non-native species such as cheatgrass may be sub-dominant in the understory. Annual production and abundance of these annuals may increase drastically in years with heavy spring precipitation. Seeded species may be present. Sagebrush and/or bitterbrush are a minor component. Singleleaf pinyon and/or Utah juniper may be present to increasing. This site is susceptible to further degradation from grazing, drought, and fire.
Pathway a
Community 2.1 to 2.2
Fire reduces the shrub overstory and allows for perennial bunchgrasses to dominate the site. 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. Aroga moth infestations can also cause mortality of the mountain big sagebrush overstory.
Pathway b
Community 2.1 to 2.3
Time and lack of disturbance allows for sagebrush to increase and become decadent. Chronic drought reduces fine fuels and leads to a reduced fire frequency, allowing big sagebrush to dominate the site. Inappropriate grazing management reduces the perennial bunchgrass understory; conversely Sandberg bluegrass may increase in the understory depending on grazing management.
Pathway a
Community 2.2 to 2.1
Time and lack of disturbance and/or grazing management that favors the establishment and growth of sagebrush allows the shrub component to recover. The establishment of big sagebrush can take many years.
Pathway b
Community 2.2 to 2.4
Tree/shrub removal treatment or prescribed burning in the presence of annual grass species will reduce shrub canopy may cause a shift to Phase 2.4. A subsequent year with precipitation that is favorable to nonnative annual grasses may speed up this pathway.
Pathway a
Community 2.3 to 2.1
A change in grazing management that reduces shrubs will allow for the perennial bunchgrasses in the understory to increase. Heavy late-fall/winter grazing may cause mechanical damage and subsequent death to sagebrush, facilitating an increase in the herbaceous understory. Aroga moth infestation, release from growing season herbivory or drought or combinations of these allows for perennial bunchgrasses to increase as well. 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 this community.
Pathway b
Community 2.3 to 2.2
Fire reduces or eliminates the overstory of sagebrush and allows for the understory perennial grasses to increase. Fires will typically be low severity resulting in a mosaic pattern due to low fine fuel loads. Following an unusually wet spring or a change in management favoring an increase in fine fuels, a fire may be more severe and reduce the shrub component to trace amounts. Annual non-native species respond well to fire and may increase post-burn.
State 3
Shrub State
This state has one community phase and is the product of many years of heavy grazing during time periods harmful to deep-rooted perennial bunchgrasses. With a reduction in deep-rooted perennial bunchgrass competition, bluegrasses and squirreltail will increase and become the dominant grass. Sagebrush dominates the overstory. Bitterbrush and/or rabbitbrush may be significant components. Sagebrush cover exceeds site concept and may be decadent, reflecting stand maturity and lack of seedling establishment due to competition with mature plants. Bare ground is also increasing. The shrub overstory and bluegrass understory dominate site resources such that soil water, nutrient capture, nutrient cycling and soil organic matter are temporally and spatially redistributed.
Community 3.1
Community Phase (at risk)
Figure 10. Fractured Stony Loam 14+ (R028BY026NV) T.Stringham July 2013
This site is at risk of transitioning to another state. Mountain big sagebrush, possibly decadent, dominates overstory and rabbitbrush may be a significant component. Deep-rooted perennial bunchgrasses may be present in trace amounts or absent from the community. Utah juniper may be present or increasing. Annual non-native species are present to increasing. Understory may be sparse, with bare ground increasing. Utah juniper or singleleaf pinyon may be present as a result of encroachment from neighboring sites and lack of disturbance.
State 4
Annual State
This state has two community phases. One phase is characterized by the dominance of annual non-native species such as cheatgrass and tansy mustard. The second phase has either mountain big sagebrush and/or rabbitbrush dominating the overstory with an understory of annual non-natives.
Community 4.1
Community Phase
Annual non-native plants such as tansy mustard and cheatgrass dominate this phase.
Community 4.2
Community Phase
Mountain big sagebrush and/or sprouting shrubs dominate the overstory. Annual non-native plants such as tansy mustard and cheatgrass dominate the understory. Trace amounts of desirable bunchgrasses may be present. The mountain big sagebrush may be old and decadent of this transitioned from State 2.3.
Pathway a
Community 4.1 to 4.2
Time and lack of fire allows for sagebrush/rabbitbrush to establish. Probability of sagebrush establishment is dependent on a near-by seed source from unburned patches of sagebrush.
Pathway a
Community 4.2 to 4.1
Fire reduces or eliminates the overstory shrub component and allows for annual non-native species to dominate the phase.
State 5
Seeded State
This state has three community phases a grass-dominated phase; a grass-shrub phase and a shrub dominated phase. The state is characterized by the dominance of seeded species such as smooth brome and crested wheatgrass. Other seeded species include forage kochia, Wyoming big sagebrush, and native and non-native perennial forbs.
Community 5.1
Community Phase
Introduced grass species and other non-native species such as forage kochia dominate the community. Native and non-native seeded forbs may be present. Trace amounts of big sagebrush may be present, especially if seeded. Annual non-native species present.
Community 5.2
Community Phase
Sprouting shrubs such as rabbitbrush and seeded species co-dominate. Annual non-native species stable to increasing. Sagebrush may be a minor component.
Community 5.3
Community Phase (at risk)
This community phase is at risk of crossing a threshold and transitioning to another state. Wyoming sagebrush dominates. Rabbitbrush may be a significant component. Seeded grass vigor and density are reduced. Annual non-native species stable to increasing. Utah juniper and/or singleleaf pinyon may be present. This site is susceptible to further degradation from grazing, drought, and fire.
Pathway a
Community 5.1 to 5.2
Inappropriate grazing management, particularly during the growing season, reduces perennial bunchgrass vigor and density and facilitates shrub establishment.
Pathway a
Community 5.2 to 5.1
Low severity fire, brush management, and/or Aroga moth infestation will reduce the sagebrush overstory and allow seeded species to become dominant.
Pathway b
Community 5.2 to 5.3
Absence of fire over time, coupled with inappropriate grazing management that promotes a reduction in perennial bunchgrasses and facilitates shrub dominance.
Pathway a
Community 5.3 to 5.1
Fire eliminates/reduces the overstory of sagebrush and allows for the understory perennial grasses to increase. Fires will typically be low severity resulting in a mosaic pattern due to low fine fuel loads. A fire following an unusually wet spring or change in management favoring an increase in fine fuels, may be more severe and reduce the shrub component to trace amounts. A severe infestation of Aroga moth will also cause a large decrease in sagebrush within the community, giving a competitive advantage to the perennial grasses and forbs. Brush treatments with minimal soil disturbance will also decrease sagebrush and release the perennial understory. Annual non-native species respond well to fire and may increase post-burn.
Transition A
State 1 to 2
Trigger: This transition is caused by the introduction of non-native annual weeds, such as cheatgrass. 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 3
Trigger: Inappropriate, long-term grazing of perennial bunchgrasses during growing season would favor shrubs and initiate transition to Community Phase 3.1. Slow variables: Long term decrease in deep-rooted perennial grass density. Threshold: Loss of deep-rooted perennial bunchgrasses changes spatial and temporal nutrient cycling and nutrient redistribution, and reduces soil organic matter.
Transition B
State 2 to 4
Trigger: Fire and/or multiple fires lead to plant community phase 4.1, inappropriate grazing management that favors shrubs in the presence of non-native annual species leads to community phase 4.2. Slow variables: Increased production and cover of non-native annual species. Threshold: Cheatgrass or other non-native annuals dominate understory
Restoration pathway A
State 3 to 2
Sagebrush removal by mechanical or chemical treatments such as brush beating and/or herbicide usually coupled with seeding of perennial bunchgrass species. This restoration leads to Community Phase 2.4.
Conservation practices
| Brush Management | |
|---|---|
| Range Planting |
Transition A
State 3 to 4
Trigger: To Community Phase 4.1: Severe fire. To Community Phase 4.2: Inappropriate grazing management in the presence of annual non-native species. Slow variables: Increased production and cover of non-native annual species. Threshold: Increased continuous fine fuels modify the fire regime by changing intensity, size, and spatial variability of fires. Changes in plant community composition and spatial variability of vegetation due to the loss of perennial bunchgrasses and sagebrush truncate energy capture spatially and temporally thus impacting nutrient cycling and distribution.
Restoration pathway A
State 4 to 5
Seeding of deep-rooted bunchgrasses, coupled herbicide. Brush treatments may be applied if needed. Probability of success is extremely low.
Conservation practices
| Brush Management | |
|---|---|
| Range Planting |
Transition A
State 5 to 4
Trigger: Catastrophic fire. Slow variables: Increased production and cover of non-native annual species. Threshold: Increased continuous fine fuels modify the fire regime by changing intensity, size, and spatial variability of fires. Changes in plant community composition and spatial variability of vegetation due to the loss of perennial bunchgrasses and sagebrush truncate energy capture spatially and temporally, thus impacting nutrient cycling and distribution.
Additional community tables
Table 6. Community 1.1 plant community composition
| Group | Common name | Symbol | Scientific name | Annual production (lb/acre) | Foliar cover (%) | |
|---|---|---|---|---|---|---|
|
Grass/Grasslike
|
||||||
| 1 | Primary Perennial Grasses | 153–1926 | ||||
| bluebunch wheatgrass | PSSPS | Pseudoroegneria spicata ssp. spicata | 90–180 | – | ||
| bluegrass | POA | Poa | 18–72 | – | ||
| Thurber's needlegrass | ACTH7 | Achnatherum thurberianum | 23–68 | – | ||
| western needlegrass | ACOC3 | Achnatherum occidentale | 22–67 | – | ||
| 2 | Secondary Perennial Grasses | 18–90 | ||||
| Indian ricegrass | ACHY | Achnatherum hymenoides | 5–27 | – | ||
| Columbia needlegrass | ACNE9 | Achnatherum nelsonii | 5–27 | – | ||
| squirreltail | ELEL5 | Elymus elymoides | 5–27 | – | ||
|
Forb
|
||||||
| 3 | Perennial | 45–135 | ||||
| arrowleaf balsamroot | BASA3 | Balsamorhiza sagittata | 5–27 | – | ||
| tapertip hawksbeard | CRAC2 | Crepis acuminata | 5–27 | – | ||
| lupine | LUPIN | Lupinus | 5–27 | – | ||
|
Shrub/Vine
|
||||||
| 4 | Primary Shrubs | 423–747 | ||||
| Utah serviceberry | AMUT | Amelanchier utahensis | 315–405 | – | ||
| mountain big sagebrush | ARTRV | Artemisia tridentata ssp. vaseyana | 45–135 | – | ||
| antelope bitterbrush | PUTR2 | Purshia tridentata | 45–135 | – | ||
| snowberry | SYMPH | Symphoricarpos | 18–72 | – | ||
| 5 | Secondary Shrubs | 18–72 | ||||
| yellow rabbitbrush | CHVI8 | Chrysothamnus viscidiflorus | 9–27 | – | ||
| chokecherry | PRVI | Prunus virginiana | 9–27 | – | ||
Interpretations
Animal community
Livestock Interpretations:
This site is suitable for livestock grazing. Considerations for grazing management including timing, intensity and duration of grazing. Targeted grazing could be used to decrease the density of non-natives.
Bluebunch wheatgrass is considered one of the most important forage grass species on western rangelands for livestock. Although bluebunch wheatgrass can be a crucial source of forage, it is not necessarily the most highly preferred species. Bluebunch wheatgrass is moderately grazing tolerant and is very sensitive to defoliation during the active growth period (Blaisdell and Pechanec 1949, Laycock 1967, Anderson and Scherzinger 1975 Britton et al. 1990). Herbage and flower stalk production was reduced with clipping at all times during the growing season; however, clipping was most harmful during the boot stage (Blaisdell and Pechanec 1949, Britton et al. 1990)). Tiller production and growth of bluebunch was greatly reduced when clipping was coupled with drought (Busso and Richards 1995). Mueggler (1975) estimated that low vigor bluebunch wheatgrass may need up to 8 years rest to recover. Although an important forage species, it is not always the preferred species by livestock and wildlife.
Thurber’s needlegrass species begin growth early in the year and remain green throughout a relatively long growing season. This pattern of development enables animals to use Thurber’s needlegrass when many other grasses are unavailable. Cattle prefer Thurber’s needlegrass in early spring before fruits have developed as it becomes less palatable when mature. Thurber’s needlegrasses are grazed in the fall only if the fruits are softened by rain. Thurber’s needlegrass is sensitive to defoliation, especially during the boot stage (Ganskopp 1988).
Bluegrass is a widespread forage grass. It is one of the earliest grasses in the spring and is sought by domestic livestock and several wildlife species. Bluegrass is a palatable species, but its production is closely tied to weather conditions. It produces little forage in drought years, making it a less dependable food source than other perennial bunchgrasses. Muttongrass is excellent forage for domestic livestock especially in the early spring. Muttongrass begins growth in late winter and early spring, which makes it available before many other forage plants. Antelope bitterbrush is important browse for livestock. Domestic livestock and mule deer may compete for antelope bitterbrush in late summer, fall, and/or winter. Cattle prefer antelope bitterbrush from mid-May through June and again in September and October. Despite low palatability, mountain big sagebrush is eaten by sheep, cattle, goats, and horses. Chemical analysis indicates that the leaves of big sagebrush equal alfalfa meal in protein, have a higher carbohydrate content, and yield twelvefold more fat (USDA-Forest Service 1937). Antelope bitterbrush is an important shrub species to a variety of animals, such as domestic livestock, antelope, deer, and elk. Bitterbrush is critical browse for mule deer, as well as domestic livestock, antelope, and elk (Wood 1995, Clements and Young 2002). Grazing tolerance of antelope bitterbrush is dependent on site conditions (Garrison 1953).
Stocking rates vary over time depending upon season of use, climate variations, site, and previous and current management goals. A safe starting stocking rate is an estimated stocking rate that is fine-tuned by the client by adaptive management through the year and from year to year.
Wildlife Interpretations:
Many wildlife species are dependent on the sagebrush ecosystem including the greater sage grouse, sage sparrow, pygmy rabbit and the sagebrush vole. Dobkin and Sauder (2004) identified 61 species, including 24 mammals and 37 birds, associated with the shrub-steppe habitats of the Intermountain West. Mountain big sagebrush is important to wildlife for both food and cover. Mountain big sagebrush is highly preferred and nutritious winter forage for mule deer, elk and pronghorn. Elk (Alces alces) and pronghorn antelope (Antilocapra americana) prefer mountain big sagebrush over basin and Wyoming sagebrush (Beale and Smith 1970, Wambolt 1996). A study by Brown (1977) determined that desert bighorn sheep (Ovis canadensis nelisoni) preferred big sagebrush over other shrub types; however, the variety was not noted. Welch and Wagstaff (1992) noted in a study near Provo, Utah, mountain big sagebrush was highly preferred winter forage of mule deer (Odocoileus hemionus) over other available forage. Other studies have determined, in the same study area, that mountain big sagebrush is preferred by both wintering domestic sheep as well as mule deer (Welch et al. 1986).
Furthermore, wildlife use a variety of associated understory plants and soils that occur in basin big sagebrush habitat. For example: sage grouse (Centrocercus urophasianus), sagebrush vole (Lemmiscus curtatus), Merriam’s shrew (Sorex merriami) and Preble’s shrew (Sorex preblei) use the grasses that occur with mountain big sagebrush for nesting, cover and forage. Mountain big sagebrush sandy soil sites provide burrowing opportunities and protection from predators for burrowing owls (Athene cunicularia), dark and pale kangaroo mice (Microdipodops megacephalus and Microdipodops pallidus, respectively). Mountain big sagebrush that occur on woodland and rock ecotnes provides nesting and foraging habitat for the ferruginous hawk (Buteo regalis) (Nevada Wildlife Action Plan 2012). Deer and elk make heavy use of muttongrass, especially in early spring when other green forage is scarce. Depending upon availability of other nutritious forage, deer may use mutton grass in all seasons. Muttongrass cures well and is an important fall and winter deer food in some areas. Canby's bluegrass is also an important forage species for several wildlife species.
Several reptiles and amphibians are distributed throughout the sagebrush steppe in the west in Nevada, where basin big sagebrush is known to grow (Bernard and Brown 1977). Reptile species including: eastern racers (Coluber constrictor), ringneck snakes (Diadophis punctatus), night snakes (Hypsiglena torquata), Sonoran mountain kingsnakes (Lampropeltis pyromelana), striped whipsnakes (Masticophis taeniatus), gopher snakes (Pituophis catenifer), long-nosed snakes (Rhinoceheilus lecontei), wandering garter snakes (Thamnophis elegans vagrans), Great Basin rattlesnakes (Crotalus oreganus lutosus), Great Basin collared lizard (Crotaphytus bicinctores), long-nosed leopard lizard (Gambelia wislizenii), short-horned lizard (Phrynosoma douglassi), desert-horned lizard (Phrynosoma platyrhinos), sagebrush lizards (Sceloporus graciosus), western fence lizards (Sceloporus occidentalis), northern side-blotched lizards (Uta uta stansburiana), western skinks (Plestiodon skiltonianus), and Great Basin whiptails (Aspidoscelis tigris) occur in areas where sagebrush is dominant. Similarly, amphibians such as: western toads (Anaxyrus boreas), Woodhouse’s toads (Anaxyrus woodhousii), northern leopard frogs (Lithobates pipiens), Columbia spotted frogs (Rana luteiventris), bullfrogs (Lithobates catesbeianus), and Great Basin spadefoots (Spea intermontana) also occur throughout the Great Basin in areas sagebrush species are dominant (Hamilton 2004). Studies have not determined if reptiles and amphibians prefer certain species of sagebrush; however, researchers agree that maintaining habitat where basin big sagebrush and reptiles and amphibians occur is important. In fact, wildlife biologists have noticed declines in reptiles where sagebrush steppe habitat has been seeded with introduced grasses (West 1999 and ref. therein).
Sagebrush communities are important for maintaining lagomorph and rodent populations. Pygmy rabbits, sagebrush obligates, use sites with big sagebrush at a higher intensity than low sagebrush sites (Heady and Laundre 2005). A study by Larrison and Johnson (1973) captured more deer mice in big sagebrush communities than in any other plant community. Although specific varieties of big sagebrush are not mentioned in these studies, thus, suggests that deer mice prefer big sagebrush plant communities where mountain big sagebrush are present, for cover over other plant communities.
It should be noted that sagebrush-grassland communities provide critical sage-grouse (Centrocercus urophaianus) breeding and nesting habitats. Meadows surrounded by sagebrush may be used as feeding and strutting grounds. Sagebrush is a crucial component of their diet year-round, and sage-grouse select sagebrush almost exclusively for cover. Sage-grouse prefer mountain big sagebrush and Wyoming big sagebrush communities to basin big sagebrush communities.
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
Utah serviceberry fruits were used by Native Americans and early European explorers in North America for food and medicine. Native Americans used big sagebrush leaves and branches for medicinal teas, and the leaves as a fumigant. Bark was woven into mats, bags and clothing. Common snowberry fruit was eaten fresh but was not favored by Native Americans in Washington and Oregon. The fruits were eaten fresh and also dried for winter use. Common snowberry was used on hair as soap, and the fruits and leaves mashed and applied to cuts or skin sores as a poultice and to soothe sore, runny eyes. Tea from the bark was used as a remedy for tuberculosis and sexually transmitted diseases. A brew made from the entire plant was used as a physic tonic. Arrowshafts and pipestems were made from the stems.
Other information
Utah serviceberry has been used to revegetate big game winter range and for surface stabilization. It grows slowly from seed and therefore transplanting may be more successful than seeding for revegetation projects. Antelope bitterbrush has been used extensively in land reclamation. Antelope bitterbrush enhances succession by retaining soil and depositing organic material and in some habitats and with some ecotypes, by fixing nitrogen.
Supporting information
Type locality
| Location 1: White Pine County, NV | |
|---|---|
| Township/Range/Section | T18N R62E S4 |
| Latitude | 39° 27′ 18″ |
| Longitude | 115° 0′ 4″ |
| General legal description | About 11 air miles east of McGill, Egan Range, White Pine County, Nevada. This site also occurs in Elko County, Nevada. |
Other references
Akinsoji, A. 1988. Postfire vegetation dynamics in a sagebrush steppe in southeastern Idaho, USA. Vegetation 78:151-155.
Anderson, E.W. and R.J. Scherzinger. 1975. Improving quality of winter forage for elk by cattle grazing. Journal of Range Management 28(2):120-125.
Blaisdell, J.P. 1953. Ecological effects of planned burning of sagebrush-grass range on the Upper Snake River Plains. Tech. Bull. 1975. Washington, DC: U.S. Department of Agriculture. 39 p.
Blaisdell, J. P. and W. F. Mueggler. 1956. Sprouting of bitterbrush (Purshia tridentata) following burning or top removal. Ecology 37:365-370.
Blaisdell, J.P. R.B. Murray, and E.D. McArthur. 1982. Managing Intermountain rangelands-- sagebrush-grass ranges. Gen. Tech. Rep. INT-134. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Forest and Range Experiment Station. 41 p.
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(3):298-305.
Britton, C.M., G.R. McPherson and F.A. Sneva. 1990. Effects of burning and clipping on five bunchgrasses in eastern Oregon. The Great Basin Naturalist 50(2):115-120.
Bunting, S.C., B.M. Kilgore, and C.L. Bushey. 1987. Guidelines for prescribed burning sagebrush/grass rangelands in the northern Great Basin. Gen. Tech. Rep. INT-231. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Research Station. 33 p.
Burkhardt, J.W. and E.W. Tisdale. 1969. Nature and successional status of western juniper vegetation in Idaho. Journal of Range Management 22(4):264-270.
Busse, D., A. Simon, and M. Riegel. 2000. Tree-growth and understory responses to low-severity prescribed burning in thinned Pinus ponderosa forests of central Oregon. Forest Science 46:258-268.
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.
Clark, R. G., M. B. Carlton, and F. A. Sneva. 1982. Mortality of bitterbrush after burning and clipping in Eastern Oregon. Journal of Range Management 35:711-714.
Clements, C. D. and J. A. Young. 2002. Restoring antelope bitterbrush. Rangelands 24:3-6.
Comstock, J.P. and J.R. Ehleringer. 1992. Plant adaptation in the Great Basin and Colorado Plateau. The Great Basin Naturalist 52:195-215.
Conrad, C.E. and C.E. Poulton. 1966. Effect of a wildfire on Idaho fescue and bluebunch wheatgrass. Journal of Range Management 19(3):138-141.
Cook, J. G., T. J. Hershey, and L. L. Irwin. 1994. Vegetative Response to Burning on Wyoming Mountain-Shrub Big Game Ranges. Journal of Range Management 47:296-302.
Crawford, J.A., R.A. Olson, N.E. West, J.C. Mosley, M.A. Schroeder, T.D. Whitson, R.F. Miller, M.A. Gregg, and C.S. Boyd. 2004. Ecology and management of sage-grouse and sage-grouse habitat. Journal of Range Management. 57: 2-19.
Dobkin, D.S. and J.D. Sauder. 2004. Shrub steppe landscapes in jeopardy. Distributions, abundances, and the uncertain future of birds and small mammals in the Intermountain West. High Desert Ecological Research Institute, Bend, Oregon. USA.
Driscoll, R. S. 1964. A relict area in the central Oregon juniper zone. Ecology 45:345-353. Ganskopp, D. 1988. Defoliation of Thurber needlegrass: herbage and root responses. Journal of Range Management 41(6):472-476.
Fire Effects Information System (Online; http://www.fs.fed.us/database/feis/plants/).
Ganskopp, D., L. Aguilera, and M. Vavra. 2007. Livestock forage conditioning among six northern Great Basin grasses. Rangeland Ecology and Management 60:71-78.
Garrison, G. A. 1953. Effects of Clipping on Some Range Shrubs. Journal of Range Management 6:309-317.
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.
Houston, D.B. 1973. Wildfires in northern Yellowstone National Park. Ecology 54(5):1111-1117. Hurd, R.M. 1961. Grassland vegetation in the Big Horn Mountains, Wyoming. Ecology 42(3):459-467.
Kerns, B. K., W. G. Thies, and C. G. Niwa. 2006. Season and severity of prescribed burn in ponderosa pine forests: implications for understory native and exotic plants. Ecoscience 13:44-55.
Koniak, S. 1985. Succession in piñon-juniper woodlands following wildfire in the Great Basin. The Great Basin Naturalist 45(3):556-566.
Krall, J.L., J.R. Stroh, C.S. Cooper, and S.R. Chapman. 1971. Effect of time and extent of harvesting basin wildrye. Journal of Range Management 24(6):414-418.
Kuntz, D.E. 1982. Plant response following spring burning in an Artemisia tridentata subsp. vaseyana/Festuca idahoensis habitat type. Moscow, ID: University of Idaho. 73 p. Thesis.
Laycock, W.A. 1967. How heavy grazing and protection affect sagebrush-grass ranges. Journal of Range Management 20:206-213.
Majerus, M. E. 1992. High-stature grasses for winter grazing. Journal of soil and water conservation 47:224-225.
McConnell, B. R. 1961. Notes on some rooting characteristics of antelope bitterbrush. Res. Note No. 204. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station. 5 p.
McConnell, B. R. and J. G. Smith. 1977. Influence of grazing on age-yield Interactions in bitterbrush. Journal of Range Management 30:91-93.
Miller, R.F., T.J. Svejcar, and J.A. Rose. 2000. Impacts of western juniper on plant community composition and structure. Journal of Range Management 53(6):574-585.
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. Gen. Tech. Rep. RMRS-GTR-308. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station. 126 p.
Murray, R. 1983. Response of antelope bitterbrush to burning and spraying in southeastern Idaho. Tiedemann, Arthur R.; Johnson, Kendall L., compilers. Research and management of bitterbrush and cliffrose in western North America. General Technical Report INT-152. Ogden, UT: US Department of Agriculture, Forest Service, Intermountain Forest and Range Experiment Station: 142-152.
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/
Neuenschwander, L.F. 1980. Broadcast burning of sagebrush in the winter. Journal of Range Management (33)3:233-236.
Noste, N.V. and C.L. Bushey. 1987. Fire response of shrubs of dry forest habitat types in Montana and Idaho. Gen. Tech. Rep. INT-239. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Research Station. 22 p.
Richards, J. H. and M. M. Caldwell. 1987. Hydraulic lift: substantial nocturnal water transport between soil layers by Artemisia tridentata. Oecologia. 73(4): 486-489.
Robberecht, R. and G.E. Defosse. 1995. The relative sensitivity of two bunchgrass species to fire. International Journal of Wildland Fire 5(3):127-134.
Smith, M.A. and F. Busby. 1981. Prescribed burning: effective control of sagebrush in Wyoming. RJ-165. Laramie, WY: University of Wyoming, Agricultural Experiment Station. 12 p.
Stringham, T.K., P. Novak-Echenique, P. Blackburn, C. Coombs, D. Snyder and A. Wartgow. 2015. Final Report for USDA Ecological Site Description State-and-Transition Models, Major Land Resource Area 28A and 28B Nevada. University of Nevada Reno, Nevada Agricultural Experiment Station Research Report 2015-01. p. 1524.
Tirmenstein, D. 1999. Achnatherum hymenoides. In: Fire Effects Information System. [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory. http://www.fs.fed.us/database/feis.
USDA–Forest Service. 1937. Range Plant Handbook. Dover Publications, New York. 816 p.
USDA-NRCS Plants Database (Online; http://www.plants.usda.gov).
Wood, M. K., Bruce A. Buchanan, & William Skeet. 1995. Shrub preference and utilization by big game on New Mexico reclaimed mine land. Journal of Range Management 48:431-437.
Wright, H. A. 1971. Why squirreltail is more tolerant to burning than needle-and-thread. Journal of Range Management 24:277-284.
Young, R.P. 1983. Fire as a vegetation management tool in rangelands of the Intermountain Region. In: Monsen, S.B. and N. Shaw (compilers). Managing Intermountain rangelands-- improvement of range and wildlife habitats: Proceedings; 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.
Zschaechner, G.A. 1985. Studying rangeland fire effects: a case study in Nevada. In: Sanders, K. and J. Durham (eds). Rangeland fire effects. Proceedings of the symposium. 1984 November 27- 29; Boise, ID. Boise, ID. U.S. Department of the Interior, Bureau of Land Management, Idaho State Office. pp 66-84.
Contributors
RK
Rangeland 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) | P.NOVAK-ECHENIQUE |
|---|---|
| Contact for lead author | STATE RANGELAND MANAGEMENT SPECIALIST |
| Date | 03/24/2015 |
| Approved by | |
| Approval date | |
| Composition (Indicators 10 and 12) based on | Annual Production |
Indicators
-
Number and extent of rills:
Rills are none to rare. A few rills can be expected on steeper slopes in areas subjected to summer convection storms or rapid spring snowmelt. These will begin to heal during the next growing season. -
Presence of water flow patterns:
Water flow patterns are none to rare but can be expected in areas subjected to summer convection storms or rapid snowmelt usually on steeper slopes. flow paths are typically short (<1m), meandering and not connected. They are interrupted by plants and surface rock fragments. -
Number and height of erosional pedestals or terracettes:
Pedestals are rare. Occurrence is usually limited to areas of water flow patterns. Frost heaving of shallow rooted plants should not be considered a "normal" condition. -
Bare ground from Ecological Site Description or other studies (rock, litter, lichen, moss, plant canopy are not bare ground):
Bare Ground up to 30 % depending on amount of surface rock fragments. -
Number of gullies and erosion associated with gullies:
None -
Extent of wind scoured, blowouts and/or depositional areas:
None -
Amount of litter movement (describe size and distance expected to travel):
Fine litter (foliage from grasses and annual & perennial forbs) expected to move distance of slope length during intense summer convection storms or rapid snowmelt events. Persistent litter (large woody material) will remain in place except during large rainfall events. -
Soil surface (top few mm) resistance to erosion (stability values are averages - most sites will show a range of values):
Soil stability values should be 4 to 6 on most soil textures found on this site -
Soil surface structure and SOM content (include type of structure and A-horizon color and thickness):
Surface structure is typically fine and medium granular. Soil surface colors are dark grayish browns and soils are typified by a mollic epipedon. Surface textures are loams. Organic matter of the surface 2 to 4 inches is typically 1 to 3 percent dropping off quickly below. Organic matter content can be more or less depending on micro-topography. -
Effect of community phase composition (relative proportion of different functional groups) and spatial distribution on infiltration and runoff:
Perennial herbaceous plants, especially deep-rooted bunchgrasses (bluebunch wheatgrass, needlegrass), slow runoff and increase infiltration. Shrub canopy and associated litter break raindrop impact and provide opportunity for snow catch and accumulation on site. -
Presence and thickness of compaction layer (usually none; describe soil profile features which may be mistaken for compaction on this site):
Compacted layers are none. Subanuglar blocky or massive structure or subsoil argillic horizons are not to be interpreted as compacted. -
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:
Reference Plant Community: tall shrubs (Utah serviceberrry, bitterbrush, big sagebrush)Sub-dominant:
Deep-rooted, cool season, perennial bunchgrasses >> associated shrubs > deep-rooted perennial forbs > shallow-rooted perennial grasses > fibrous, shallow-rooted, cool season, perennial and annual forbsOther:
Additional:
With an extended fire return interval, the shrub component will increase at the expense of the herbaceous component. -
Amount of plant mortality and decadence (include which functional groups are expected to show mortality or decadence):
Dead branches within individual shrubs common and standing dead shrub canopy material may be as much as 25% of total woody canopy; some of the mature bunchgrasses (<10%) have dead centers. -
Average percent litter cover (%) and depth ( in):
Between plant interspaces (20-30%) and litter depth is < ½ inch. -
Expected annual annual-production (this is TOTAL above-ground annual-production, not just forage annual-production):
For normal or average growing season (through June) ±900 lbs/ac. Favorable years ±1200 lbs/ac and unfavorable years ±700 lbs/ac. -
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:
Potential invaders include cheatgrass, Russian thistle, annual mustards and knapweeds. -
Perennial plant reproductive capability:
All functional groups should reproduce in average (or normal) and above average growing season years. Little growth or reproduction occurs during extreme drought years.
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