The Transition from Mojave Desert to Great Basin Desert on the Nevada Test Site D. J. Hansen W. K. Ostler D.B. Hall Abstract—Plant species and associations on the Nevada Test Site are located along elevation and precipitation gradients. Associations in the Great Basin Desert had the highest species diversity. Rodent sign and productivity of annual plants are least in the lower and higher elevations and most abundant in the mid-elevations. Microbiotic crusts are most abundant in fine-textured soils and of low abundance in soils with active erosional processes. Texture of surface soils (0 to 5 centimeters [0 to 2 inches]) differs little among all associations except for a few that are correlated with playas and steep mountain slopes. However, differences among associations are observed for deeper substrates comprised of limestone, basalt, and tuff parent materials. The Nevada Test Site (NTS) is located about 105 km (65 miles) northwest of Las Vegas in southern Nevada (see fig. 1 of companion paper, Ostler and others, 1999). The site was created by a series of land withdrawals in the early 1950s for nuclear weapons testing. It comprises a total land area of 350,000 ha (1,350 square miles). Despite nearly 1,000 atmospheric and below-ground nuclear tests, the area is relatively undisturbed and offers an excellent location for biological studies. The area has had limited or no livestock grazing since the 1950s and is designated as a National Environmental Research Park. The NTS consists of three large valleys, Yucca, Frenchman, and Jackass Flats. It has two high mesas, Rainier and Pahute. It has a rough elevational gradient from south to north with the lowest point at 829 m (2,688 ft) in Jackass Flats and the highest point at 2,340 m (7,679 ft) on Rainier Mesa. The site straddles the Mojave and Great Basin Deserts and provides an excellent site to observe the transition between these two deserts. Numerous detailed studies have been conducted on NTS biota focusing primarily on inventories and evaluating the effects of nuclear testing. Approximately 730 plant species occur on the NTS, of which several are sensitive or protected. Methods _______________________ Shrublands of the NTS were classified using methods described in a companion paper presented in these proceedings In: McArthur, E. Durant; Ostler, W. Kent; Wambolt, Carl L., comps. 1999. Proceedings: shrubland ecotones; 1998 August 12–14; Ephraim, UT. Proc. RMRS-P-11. Ogden, UT: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station. D. J. Hansen, W. K. Ostler, and D. B. Hall are Biologists with Bechtel Nevada, P.O. Box 98521, M/S NLV-081, Las Vegas, NV 89193-8521. 148 (Ostler and others 1999). Approximately 1,500 ecological landform units (ELUs) were delineated using aerial photography and satellite imagery to distinguish ecological mapping types. The boundaries of each ELU were field verified. Landforms were selected because they are highly correlated with soil types in Nevada (Peterson 1981) and have been used historically to help classify habitat types in the Mojave Desert (Berry 1979). Vegetation and other site parameters were sampled within representative areas of each ELU. Data were analyzed using cluster analyses and descriptive statistics to help classify vegetation into 10 alliances and 20 associations. Results ________________________ Results of the vegetation classification on the NTS are shown in table 1. About 23 percent and 37 percent of the ELUs sampled on the NTS were located in the Mojave Desert and Great Basin Desert, respectively (table 2). The remaining 36 percent of the ELUs were located in a Transition Zone between these two deserts. About 4 percent of the 1,508 ELUs sampled were classified as “miscellaneous” because they were unique vegetation types, burned, scraped, or disturbed by nuclear testing. In the Mojave Desert the Larrea tridentata/Ambrosia dumosa Shrubland was the most numerous association representing about 19 percent of the ELUs on the NTS (18 percent of the total area). No other association in the Mojave Desert represented more than 4 percent of the total ELUs. In the Great Basin Desert the Artemisia tridentata-Chrysothamnus viscidiflorus Shrubland was the most numerous association representing about 11 percent of the ELUs on the NTS (7.5 percent of the total area). No other association in the Great Basin Desert represented more than 7 percent of the total ELUs. In the Transition Zone between these deserts, the Coleogyne ramosissima-Ephedra nevadensis Shrubland was the most numerous association representing about 22 percent of the ELUs on the NTS (21.6 percent of the total area). No other association in the Transition Zone represented more than 6 percent of the total ELUs. Distribution of Plant Alliances on the Nevada Test Site Figure 1 shows the distribution of plant alliances on the NTS. Also shown are the generalized boundaries for the Mojave Desert, Great Basin Desert, and the Transition Zone between these deserts. Plant species that dominate associations within the Transition Zone have been historically USDA Forest Service Proceedings RMRS-P-11. 1999 Table 1—Classification of vegetation on the Nevada Test Site. Mojave Desert Lycium spp. Shrubland Alliance Lycium shockleyi-Lycium pallidum Shrubland Larrea tridentata/Ambrosia dumosa Shrubland Alliance Larrea tridentata /Ambrosia dumosa -Shrubland Atriplex confertifolia - Ambrosia dumosa Shrubland Alliance Atriplex confertifolia - Ambrosia dumosa Shrubland Transition Zone Hymenoclea -Lycium Shrubland Alliance Lycium andersonii - Hymenoclea salsola Shrubland Hymenoclea salsola - Ephedra nevadensis Shrubland Ephedra nevadensis Shrubland Alliance Menodora spinescens - Ephedra nevadensis Shrubland Krascheninnikovia lanata - Ephedra nevadensis Shrubland Eriogonum fasciculatum - Ephedra nevadensis Shrubland Ephedra nevadensis - Grayia spinosa Shrubland Coleogyne ramosissima Shrubland Alliance Coleogyne ramosissima - Ephedra nevadensis Shrubland Great Basin Desert Atriplex spp. Shrubland Alliance Atriplex confertifolia - Kochia americana Shrubland Atriplex canescens - Krascheninnikovia lanata Shrubland Chrysothamnus-Ericameria Shrubland Alliance Chrysothamnus viscidiflorus - Ephedra nevadensis Shrubland Ericameria nauseosa Shrubland Alliance Ericameria nauseosa - Ephedra nevadensis Shrubland Artemisia spp. Shrubland Alliance Ephedra viridis - Artemisia tridentata Shrubland Artemisia tridentata - Chrysothamnus viscidiflorus Shrubland Artemisia nova - Chrysothamnus viscidiflorus Shrubland Artemisia nova - Artemisia tridentata Shrubland Pinus monophylla/Artemisia spp. Woodland Alliance Pinus monophylla/Artemisia nova Woodland Pinus monophylla/Artemisia tridentata Woodland deciduous (e.g., blackbrush) or have essentially leafless, photosynthetic stems (e.g., Ephedra spp.), while the most abundant dominant shrubs from associations in the Mojave Desert and Great Basin Desert are evergreen in habit (e.g., creosote bush, big sagebrush, singleleaf pinyon, and Utah juniper). The evolutionary adaptation of leaf reduction or abscission during drought and stress-induced dormancy may help maintain the abundance of blackbrush and Mormon tea (Ephedra nevadensis) in these ecotones. While the abundance of species other than blackbrush are relatively low in the Coleogyne ramosissima - Ephedra nevadensis Shrubland, they are frequently present in small numbers being found in small patches where animals have disturbed the soil horizons or fire has reduced competition with blackbrush. Blackbrush occurs at intermediate elevations. At these elevations lightning strikes, associated with storms blowing from the south, are common during the summer and occasionally fuel loading reaches levels high enough to support wildfires. Once burned these communities reestablish very slowly; this phenomenon is also reported by Brown (1982). Species Diversity Species diversity (richness or the number of species) of perennial trees and shrubs was greatest in the Great Basin Desert associations (mean of 56 species) compared to associations in the Transition Zone (mean of 49 species) and the Mojave Desert (mean of 36 species). Similar species diversity patterns were also observed for all combined perennial species on the NTS (table 2) (e.g., Great Basin Desert: 21.7 species per ELU, Transition Zone: 17.4 species per ELU, and Mojave Desert: 12.7 species per ELU). Elevation and Precipitation associated with either desert, and in some cases, listed as a minor species in both deserts. Associations that were considered typical or characteristic of the Mojave Desert were those that contained a presence of Shockley’s desertthorn (Lycium shockleyi), rabbit thorn (Lycium pallidum), creosote bush (Larrea tridentata), or white bursage (Ambrosia dumosa), but lacked species characteristic of the Great Basin Desert (table 3). The distribution of creosote bush on the NTS (fig. 2) approximates the boundaries for the Mojave Desert on the NTS. Associations that were considered typical of the Great Basin Desert were those that contained a presence of sagebrush (Artemisia spp.), singleleaf pinyon (Pinus monophylla), or Utah juniper (Juniperus osteosperma), but lacked species characteristic of the Mojave Desert. The distribution of big sagebrush (Artemisia tridentata) on the NTS (fig. 3) approximates the boundaries of the Great Basin on the NTS. Associations within the Transition Zone were considered to be those that had a mixture of species, many species occurring in both the Mojave and Great Basin Desert (table 3), such as Ephedra (Ephedra) spp. and blackbrush, (Coleogyne ramosissima). The distribution of blackbrush on the NTS (fig. 4) approximates the boundaries of the Transition Zone on the NTS. Associations that occur in the Transition Zone appear to be comprised of shrubs that are predominantly drought USDA Forest Service Proceedings RMRS-P-11. 1999 Plant associations within the Mojave Desert and Great Basin Desert were ordered according to increasing elevation and precipitation (fig. 5). Mean annual precipitation was 2 determined to be positively correlated (r = 0.85) with elevation on the NTS, based on correlation modeling and actual weather recording data (French 1986; other detailed meteorological data are presented by Fransioli and Ambos 1997). The importance of elevation, slope, and substrate in accounting for statistical variance in shrub species cover was also described for the Nellis Air Force Range consisting of 2 1,228,355 ha (7,432 mi ) of shrubland adjacent to the NTS (Pritchett and others 1997). Soils and Parent Materials Texture of surface soils (0 to 5 centimeters [0 to 2 inches]) appeared to differ little among all associations except for two that were correlated with playas and steep mountain slopes. The plant associations associated with playas were the Lycium shockleyi - Lycium pallidum Shrubland and the Atriplex confertifolia - Kochia americana Shrubland. Soil texture of these associations had a greater percentage of clay than other associations. The most abundant soil textures for surface soils of the associations were comprised of three textural types: sandy loam (30 percent), loamy sand 149 Number of stands Number of shrub species Mean number of perennial species/ELU Mean elevation (m) Mean precipitation (cm) Mean slope (degrees) Mean rock pavement (percent) Parameters Lycium shockleyi-Lycium pallidum 4 11 8.8 941 14.8 0.8 32.5 Larrea tridentata/Ambrosia dumosa 287 49 13.2 1,080 16 5.7 63.2 Atriplex confertifolia-Ambrosia dumosa 51 49 16.2 1,153 16.9 13.6 57.4 Menodora spinescens-Ephedra nevadensis 42 50 19.4 1,198 17.5 8 65 Krascheninnikovia lanata-Ephedra nevadensis 29 34 17.6 1,258 18.2 3.6 58.1 11 23 12.8 1,263 18.3 2.3 55.5 Lycium andersonii-Hymenoclea salsola 44 50 15.2 1,263 18.3 3.8 47.6 Eriogonum fasciculatum - Ephedra nevadensis 14 36 20.4 1,292 18.7 36.3 17.5 Transition zone Hymenoclea salsola-Ephedra nevadensis Mojave Desert Ephedra nevadensis-Grayia spinosa 93 66 19.7 1,413 20.2 8.8 57 Coleogyne ramosissima-Ephedra nevadensis 325 84 16.9 1,385 19.8 8.5 68.2 Atriplex confertifolia-Kochia americana 17 53 9.2 1,208 17.6 2.7 34.1 38 87 11.9 1,237 18 3.5 41.1 Atriplex canescens-Krascheninnikovia lanata Table 2—Parameters associated with associations in the Mojave and Great Basin Deserts and Transition Zone on the Nevada Test Site. 76 61 21.4 1,485 21.1 7.1 57.2 Chrysothamnus viscidiflorus-Ephedra Nevadensis 150 USDA Forest Service Proceedings RMRS-P-11. 1999 43 17.1 1,563 22.1 6.9 62.8 42 27 1,719 24 18.2 49.8 73 20.8 1,776 24.7 5.9 52.5 56 24.7 1,805 25.1 6.4 66.7 Great Basin Desert 47 29.1 1,831 25.4 8.6 47.8 54 27 1,985 27.3 8.1 53.5 47 28.6 2,054 28.2 14.3 47.8 Figure 1—Vegetation alliances on the Nevada Test Site. (1 = Pinus monophylla/Artemisia spp. woodland; 2 = Artemisia spp. shrubland; 3 = Atriplex spp. shrubland; 4 = Chrysothamnus-Ericameria shrubland; 5 = Coleogyne ramosissima shrubland; 6 = Ephedra nevadensis shrubland; 7 = Lycium spp. shrubland; 8 = Hymenoclea-Lycium shrubland; 9 = Atriplex confertifolia-Ambrosia dumosa shrubland; 10 = Larrea tridentata/Ambrosia dumosa shrubland; 11 = Miscellaneous; 12 = Playa/Disturbances). USDA Forest Service Proceedings RMRS-P-11. 1999 151 Lycium shockleyi Lycium pallidum Ambrosia dumosa Larrea tridentata Krameria erecta Menodora spinescens Grayia spinosa Krascheninnikovia lanata Lycium andersonii Hymenoclea salsola Eriogonum fasciculatum Coleogyne ramosissima Ericameria cooperii Ephedra nevadensis Artemisia spinescens Atriplex confertifolia Kochia americana Atriplex canescens Chrysothamnus viscidiflorus spp. Ericameria nauseosa Ephedra viridis Purshia stansburiana Purshia glandulosa Artemisia tridentata Artemisia nova Chrysothamnus viscidiflorus spp. Leptodactylon pungens Juniperus osteosperma Purshia tridentata Pinus monophylla Parameters Lycium shockleyi-Lycium pallidum 1.0 7.5 0.5 9.0 0.0 3.5 47.5 17.0 12.5 Larrea tridentata/Ambrosia dumosa 0.0 0.0 0.4 0.1 0.5 5.5 43.4 12.4 6.6 1.3 2.1 3.3 3.0 1.7 0.4 0.6 0.6 7.1 0.1 2.7 Atriplex confertifolia-Ambrosia dumosa 0.0 0.0 0.0 15.6 4.2 3.8 1.8 0.6 4.4 6.4 1.2 0.8 3.6 0.2 8.9 0.7 31.3 0.1 0.3 0.5 Menodora spinescens-Ephedra nevadensis 0.0 0.2 0.8 2.7 10.3 3.4 4.5 13.9 1.1 3.6 4.5 2.7 0.5 4.7 0.5 11.8 0.6 8.2 Krascheninnikovia lanata-Ephedra nevadensis 0.1 2.5 2.2 4.0 2.4 0.8 2.2 8.3 28.5 8.0 3.7 0.1 1.9 1.2 12.3 5.2 4.7 Lycium andersonii-Hymenoclea salsola 6.4 0.6 2.6 0.4 6.4 1.5 1.1 2.4 0.4 0.4 5.3 7.3 51.8 9.6 0.2 4.6 5.4 0.5 0.5 0.6 8.5 0.2 0.5 1.9 2.5 4.5 51.5 0.1 1.6 0.0 0.4 2.2 1.6 0.3 Hymenoclea salsola-Ephedra nevadensis Transition zone 0.3 0.2 0.4 2.2 0.3 3.0 3.0 5.3 0.3 5.0 0.0 3.7 3.7 3.4 1.3 28.1 0.7 2.3 16.4 Eriogonum fasciculatum - Ephedra nevadensis Mojave Desert Ephedra nevadensis-Grayia spinosa 0.1 3.5 1.9 1.0 1.6 2.1 1.4 3.2 2.6 0.8 56.3 0.7 9.6 0.2 1.4 0.0 0.8 1.5 0.2 1.0 0.6 0.1 1.3 0.3 0.2 0.0 0.1 0.0 0.0 8.0 5.3 0.5 1.5 0.3 0.4 1.4 0.9 0.4 0.0 0.0 0.5 0.6 0.8 0.5 8.1 3.3 5.9 7.9 1.7 4.1 4.9 22.8 0.9 0.7 Coleogyne ramosissima-Ephedra nevadensis 0.9 0.1 6.6 49.8 22.1 2.4 0.8 0.1 0.6 0.1 0.0 5.8 0.2 2.8 5.4 0.2 0.0 1.0 0.4 0.9 0.2 2.6 3.2 10.8 5.0 3.9 0.1 1.8 0.0 2.9 0.8 3.3 0.9 57.8 1.0 0.3 0.4 0.2 0.7 0.3 0.0 0.1 0.6 0.1 0.0 0.4 5.1 5.3 4.7 1.6 0.4 1.8 0.8 11.4 2.6 3.9 0.3 6.6 36.7 0.3 1.5 0.4 0.2 5.0 1.0 0.2 0.3 0.2 0.4 0.2 0.1 0.0 0.5 0.2 0.1 0.1 0.2 0.1 5.2 4.4 51.7 2.3 1.3 0.8 6.0 0.5 0.1 0.7 4.5 1.5 0.6 3.5 1.9 0.2 21.0 8.9 15.0 15.7 6.0 1.8 0.0 2.1 0.8 0.1 0.1 1.9 8.1 0.9 2.0 0.8 0.6 56.1 1.9 3.3 2.9 1.4 0.6 2.2 0.1 0.0 0.1 0.0 1.9 1.0 0.7 0.0 0.4 0.5 0.2 7.1 0.3 0.2 0.0 2.0 0.6 0.6 0.0 0.0 0.2 0.1 4.3 0.1 0.8 0.0 1.4 5.2 0.3 1.7 0.3 0.3 14.3 67.9 2.7 0.7 0.6 0.2 0.9 Great Basin Desert 5.3 0.7 11.1 Table 3—Percent abundance of dominant species found in associations in the Mojave and Great Basin Deserts on the Nevada Test Site. Atriplex confertifolia-Kochia americana 152 USDA Forest Service Proceedings RMRS-P-11. 1999 2.0 4.8 0.8 2.2 0.1 0.9 25.1 33.8 7.5 3.6 1.2 0.2 1.3 0.0 0.3 1.8 0.1 3.1 1.9 0.5 0.3 0.5 3.7 0.0 2.3 1.1 0.8 2.6 55.4 1.7 2.3 5.9 1.7 14.1 0.8 0.1 0.0 0.0 0.1 0.5 0.0 0.0 0.0 2.8 0.3 1.1 1.4 0.3 22.8 5.4 1.5 4.1 7.3 7.9 27.5 0.7 1.0 1.8 0.3 0.1 0.0 Figure 2—Distribution and percent abundance of creosote bush on the Nevada Test Site. USDA Forest Service Proceedings RMRS-P-11. 1999 153 Figure 3—Distribution and percent abundance of big sagebrush on the Nevada Test Site. 154 USDA Forest Service Proceedings RMRS-P-11. 1999 Figure 4—Distribution and percent abundance of blackbrush on the Nevada Test Site. USDA Forest Service Proceedings RMRS-P-11. 1999 155 156 USDA Forest Service Proceedings RMRS-P-11. 1999 Figure 5—Average elevation and precipitation of vegetation associations on the Nevada Test Site. (18 percent), and loam (14 percent). Soil samples from the remaining 38 percent of associations were classified into more than 30 different textural types. The Eriogonum fasiculatum - Ephedra nevadensis Shrubland was located on the steepest slopes (36 degrees) with all other associations averaging slopes less than 18 degrees, with a mean slope of 7 degrees. Despite little difference in soil texture near the soil surface, associations were observed to differ in the type of substrate upon which they most commonly appeared. The Coleogyne ramosissima - Ephedra nevadensis Shrubland and Atriplex confertifolia - Ambrosia dumosa Shrubland appeared frequently on shallow soils of limestone-derived parent materials, while most of the associations in the Great Basin Desert occurred in the basalt or tuff formations. Remaining associations occurred in alluvial soils. Creosote bush appeared to be limited by shallow soils or the presence of a caliche layer. Lunt and others (1973) suggest that big sagebrush and creosote bush have unusually high oxygen requirements, while roots of white bursage appear to require less oxygen. Microbiotic Crusts The presence of microbiotic crusts on the soil surface (i.e., nonvascular microorganisms such as algae, fungi or lichens that are frequently important for enhancing soil fertility and surface stabilization) was noted during the field surveys. Within the NTS 58 percent of the ELUs sampled had no visual evidence of microbiotic crusts, 28 percent had low visual evidence of crusts, 11 percent had moderate visual evidence of crusts, and only 4 percent had high visual evidence of microbiotic crusts. Visual evidence of crusts were observed to decrease with increases in elevation. For example, no microbiotic crusts were observed in 31 percent of sites within the Mojave Desert, 43 percent of sites within the Transition Zone and 50 percent of sites within the Great Basin Desert. Associations with high abundance of crusts also had higher percentages of soil fines (clays or silts). Low presence of crusts or their absence was associated with active soil erosional processes (e.g., along washes and steeper unstable slopes). Productivity of Annual Vegetation The presence of annual vegetation and its relative abundance were not randomly distributed across the three areas (Mojave Desert, Transition Zone, and Great Basin Desert) based on Chi-square analyses (58.6, P < 0.001, df = 4). Associations in the Mojave Desert and the Transition Zone tended to be over-represented in the moderate category (41 and 35 percent respectively) and underrepresented in the low-very low category (43 and 43 percent respectively) while associations in the Great Basin Desert tended to be overrepresented in the low-very low category (60 percent) and underrepresented in the moderate category (22 percent). Levels within the high-very high category were similar for all three areas. This is consistent with regional floras which show a greater number of annual species in drier and hotter deserts of the Southwest compared to the colder Great Basin Desert. USDA Forest Service Proceedings RMRS-P-11. 1999 Rodent Activity The absence of sign indicating burrowing rodents and the low abundance of sign (e.g., burrows and excavated soils) were found to be correlated with increasing elevation. For example, the Mojave Desert was observed to have 45 percent of the sites with none to low sign. The Transition Zone was observed to have 59 percent of the sites with none to low sign, and the Great Basin Desert was observed to have 80 percent of the sites with none to low sign Both the moderate rodent sign and the high to very high rodent sign were inversely correlated with elevation. For example, the Mojave Desert had 39 percent moderate sign and 16 percent high to very high sign. The Transition Zone had 30 percent moderate sign and 11 percent high to very high sign. The Great Basin Desert had 14 percent moderate sign and 6 percent high to very high sign. The Mojave Desert sites may have deeper soils that are more conducive to burrowing, while the rockier soils of the Transition Zone have fewer burrows. The Great Basin Desert sites have shallow soils and more severe winters that may also reduce burrowing or abundance of animals likely to burrow. Species Correlations Pairwise comparisons of species abundance at a statistical level of significance of α = 0.05 of the 718 species observed to occur on the NTS indicate that there were 447 positive interspecific associations between species and only 271 negative interspecific associations. This general trend is in agreement with earlier studies conducted using 25 circular plots of 30.5 m (100 ft) in diameter during the late 1960s at the NTS (Wallace and Romney 1972). Using Chi-squared analyses, Wallace and Romney reported a great many more positive than negative measures of association. Vegetation and Climate of the Last 45,000 Years Vegetation patterns in response to changing climatic conditions have been studied extensively on the NTS and documented through the analyses of several packrat-midden sites (Spaulding 1985). Vegetation patterns suggest that about 45 thousand years before present (k yr BP), the NTS had cooler and wetter conditions than currently; dominant plants included littleleaf mountain mahogany (Cercocarpus ledifolius), Utah juniper, sagebrush, and horsebrush (Tetradymia spp). By 35 k yr BP, limber pine (Pinus flexilis) and four-wing saltbush (Atriplex canescens) had established at the site. By 25 k yr BP, shadscale (Atriplex confertifolia), snowberry (Symphoricarpos longiflorus), and Utah Fendlerbush (Fendlerella utahensis) became more common. By 10 k yr BP, limber pine was no longer found in packratmidden samples and was replaced by the presence of singleleaf pine and increase in the abundance of Utah Juniper. Goldenweed (Haplopappus nanus), Dorr’s sage (Salvia dorii), and grizzlybear pricklypear (Opuntia erinacea) became more prevalent. During the past 5 k yr BP, creosote bush, white bursage, and other species characteristic of the Mojave Desert 157 established within the NTS area as temperatures increased and precipitation decreased. It was estimated that many Great Basin Desert trees and shrubs were displaced about 457 to 610 m (1,500 to 2,000 ft) upward in elevation to what they historically had been as the climate changed (Spaulding 1985). This climate change opened new niches for colonization by other species such as blackbrush. Ecotonal species are often adapted to a wide change in climatic conditions such as freezing temperatures as well as hot, droughty climate. Summary and Conclusions _______ Vegetation of the NTS is diverse and relatively protected from the effects of livestock grazing. Plant communities appear to respond to moisture and temperature gradients associated with elevation gradients at the site. Other secondary patterns of plant distribution are associated with adaptation to unique substrates such as playas, steep rocky slopes, and novel substrates comprised of limestone, basalt, tuff, and alluvium. Changes in temporal species patterns on the NTS have been correlated with changing climate during the past 45 thousand years. Position of species along the elevation gradient on the NTS under current climatic conditions creates a Transition Zone characterized by a diverse mixture of species. This assemblage of species is not recognized as a regional vegetation type, but appears to be shaped by climatic extremes present in both the Mojave Desert and Great Basin Desert. The width of this zone is dependent on the steepness of the elevation gradient, slope aspect, and moisture retention characteristics of the substrate. Individual species appear to be independently distributed across the NTS within both deserts and the Transition Zone. This distribution is based on species growth requirements, although assemblages of species that have similar biological and physiological needs are found together consistently enough to be considered as distinct plant communities (i.e., alliances and associations). A better knowledge of the vegetation and the environmental conditions within the Mojave Desert and Great Basin Desert helps us better appreciate the transition between these deserts with its varying temporal and spatial characteristics. 158 References _____________________ Berry, K. H. 1979. The East Mojave Desert: An example of Inventory design and habitat analysis. In: Classification, inventory, and analysis of fish and wildlife habitat—the proceedings of a national symposium; January 24-27, 1977; Phoenix, AZ; Allan Marmelstein, General Chairman. Biological Services Program, PB 299240, FWS/OBS-78/76, U.S. Fish and Wildlife Service, Washington, D.C. Brown, D. E. 1982. Biotic communities of the American Southwest—United States and Mexico. Tucson, AZ: The University of Arizona. Desert Plants. 4(1-4): 151. French, R. H. 1986. Daily, seasonal, and annual precipitation at the Nevada Test Site, Nevada. Desert Research Institute University of Nevada System, Water Resources Center Publication #45042, DOE/NV/10384-01, U.S. Department of Energy, Nevada Operations, Las Vegas, Nevada. Fransioli, P. M.; Ambos, D. S. 1997. Engineering design climatology and regional meterological conditions report. TRW Environmental Safety Systems Inc. B00000000-01717-570700066 REV00, October 2, 1997, U.S. Department of Energy, Yucca Mountain Site Characterization Office, North Las Vegas, Nevada. Lunt, O. R.; Letey, J.; Clark, S. B. 1973. Oxygen requirements for root growth in three species of desert shrubs. Ecology. 54( 6): 1356-1362. Ostler, W. Kent; Hansen, D. J.; Hall, D. J. 1999. The classification of ahrublands on the Nevada Test Site. In: McArthur, E. Durant; Ostler, W. Kent; Wambolt, Carl L. comps. 1999. Proceedings: Shrubland Ecotones. 1998 August 12-14, Ephraim, UT. Proceedings RMRS-P-000. Ogden, UT: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station. Peterson, F. F. 1981. Landforms of the Basin & Range Province, defined for soil survey. Technical Bulletin 28. Reno: University of Nevada, Nevada Agricultural Experiment Station, Max C. Fleischmann College of Agriculture. 52 pp. Pritchertt, D.; Knight, T.; Smith, F. 1997. An inventory for rare, threatened, endangered, and endemic plants and unique communities on Nellis Air Force Bombing and Gunnery Range, Clark, Lincoln, and Nye Counties, Nevada. The Nature Conservancy, U.S. Department of Defense, Legacy Resource Management Program, Nellis Air Force Base, Nevada. Spaulding, W. G. 1985. Vegetation and climates of the last 45,000 years in the vicinity of the Nevada Test Site, South-Central Nevada. U.S. Geological Survey Professional Paper 1329. U.S. Department of the Interior in cooperation with the U.S. Department of Energy. 83 p. Wallace, A.; Romney, E. M. 1972. Radioecology and ecophysiology of desert plants at the Nevada Test Site. TID-25954. United States Atomic Energy Commission, Office of Information Services, Library of Congress Catalog Card Number: 72-600110. USDA Forest Service Proceedings RMRS-P-11. 1999