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Introductory

SPECIES: Flourensia cernua | Tarbush
ABBREVIATION : FLOCER SYNONYMS : NO-ENTRY SCS PLANT CODE : FLCE COMMON NAMES : tarbush hojase blackbrush varnishbush TAXONOMY : The currently accepted scientific name for tarbush is Flourensia cernua DC. It is a member of the Compositae family. LIFE FORM : Shrub FEDERAL LEGAL STATUS : No special status OTHER STATUS : NO-ENTRY COMPILED BY AND DATE : Sara Lynn Korthuis, September 1988 LAST REVISED BY AND DATE : NO-ENTRY AUTHORSHIP AND CITATION : Korthuis, Sara Lynn. 1988. Flourensia cernua. In: Remainder of Citation

DISTRIBUTION AND OCCURRENCE

SPECIES: Flourensia cernua | Tarbush
GENERAL DISTRIBUTION : Tarbush is essentially restricted to the Chihuahuan Desert, where it may be locally or generally abundant [14]. It occurs in Arizona, California, New Mexico, Texas, and Mexico at elevations ranging from 1,312 feet (400 m) to 6,500 feet (1,981 m) [1,4,12]. ECOSYSTEMS : FRES30 Desert shrub FRES33 Southwestern shrubsteppe FRES40 Desert grasslands STATES : AZ CA NM TX MEXICO ADMINISTRATIVE UNITS : BIBE CACA FOBO GUMO WHSA BLM PHYSIOGRAPHIC REGIONS : 7 Lower Basin and Range 12 Colorado Plateau 13 Rocky Mountain Piedmont KUCHLER PLANT ASSOCIATIONS : K044 Creosotebush - tarbush K059 Trans-Pecos shrub savanna SAF COVER TYPES : NO-ENTRY SRM (RANGELAND) COVER TYPES : NO-ENTRY HABITAT TYPES AND PLANT COMMUNITIES : Tarbush is associated with creosotebush (Larrea tridentata), mesquite (Prosopis spp.), burrograss (Scleropogon brevifolius), and tobosa (Hilaria mutica). It readily replaces native grasses in desert grasslands [1,28,32].

VALUE AND USE

SPECIES: Flourensia cernua | Tarbush
WOOD PRODUCTS VALUE : NO-ENTRY IMPORTANCE TO LIVESTOCK AND WILDLIFE : Tarbush is occasionally eaten by jackrabbits and other wildlife. It is not generally used by livestock unless little else is available [26]. Mature fruit while still on the plant is poisonous to sheep, goats, and other livestock [9,10,16,26]. Cattle have reportedly died after eating the flowers and green or mature fruits [5,10]; nonfruiting plants can apparently be grazed with no ill effect [10]. Tarbush fruit and browse may also be toxic to wildlife, particularly if forced to feed on it exclusively. PALATABILITY : The peppery, bitter quality of tarbush herbage makes it unpalatable to livestock and wildlife [15,16,28]. NUTRITIONAL VALUE : Tarbush forage in an arid New Mexico range showed relatively high protein, ash, lignin, and ether extract levels. Calcium content was high and phosphorus levels met the requirements for livestock. However, goats fed a diet consisting solely of tarbush leaves became severely emaciated, indicating low nutrient content for this forage in some areas [10]. COVER VALUE : Tarbush provides much-needed shade in summer for range animals [16]. It is used for cover by the western whiptail and side-blotched lizard [23]. VALUE FOR REHABILITATION OF DISTURBED SITES : NO-ENTRY OTHER USES AND VALUES : In northern Mexico, the leaves and flower heads were used historically to make a decoction for treating indigestion [17,26]. MANAGEMENT CONSIDERATIONS : Tarbush increases in response to overgrazing. It is considered a weed in desert rangelands where it is increasing in acreage. Invasion of grasslands by tarbush and other shrubs decreases their productivity and value to livestock and wildlife, and promotes wind and sheet erosion and the formation of arroyos [9,30,31]. Biological control methods have been considered but as of 1985 no such methods had been implemented either in the United States or Mexico [9]. Low density stands (less than 80 plants/acre [200 plants/ha]) can be controlled by individual shrub treatment with herbicides. Aerial applications of dicambra or tebuthiuron have produced good results. Picloram and 2,3,6-TBA have proven less effective [11,13].

BOTANICAL AND ECOLOGICAL CHARACTERISTICS

SPECIES: Flourensia cernua | Tarbush
GENERAL BOTANICAL CHARACTERISTICS : Tarbush is a much-branched, densely leafy shrub. It grow from less than 1 foot (0.30 m) to 3 to 7 feet (1-2 m) tall. This native perennial produces a tarlike odor, hence its common name [8,16,26]. Tarbush leaves are alternate, simple, and elliptical, and are covered with small black glands.. The sticky leaves grow up to 1 incg (2.5 cm) long. The scaly stem appears white because of hairs and dried resin [16,20,26]. The composite flower heads are small, solitary, and inconspicuous. The disked flower heads lack ray flowers and are pendant [8,16,26]. The fruit is an achene. Densely hairy, relatively motile seeds are produced in small pendant clusters [2,5]. RAUNKIAER LIFE FORM : Phanerophyte Therophyte REGENERATION PROCESSES : Tarbush grows at a slow rate and can spread vegetatively. This shrub produces a relatively motile seed that can be dispersed by wind [5,6]. SITE CHARACTERISTICS : Tarbush thickets inhabit deserts, and dry soils of valleys, mesas, flats, and foothills [16,26]. It reaches its best development in heavy clay loam soils with some gravel near the surface on sites that receive some flood water. It is often found in limestone or calcareous soils. Although it grows intermixed with creosotebush, it prefers soils that are deeper (24 inches [60 cm]) than those in areas where creosotebush dominates. It also grows into fringe areas of tobosa swales [5,7,16,20]. Although only 1 foot (0.30 m) tall or less in dry areas, tarbush may reach heights of 6 feet (1.8 m) or more on favorable sites [16]. Elevations range from 3,000 to 6,500 feet (1,067-1,981m) [16]. Primarily an inhabitant of the Chihuahuan Desert, tarbush is adapted to an average annual precipitation of 9.4 inches (24 cm), 70 percent of which falls in the summer when desert plants tend to be dormant and only 20 percent of which falls in the winter [2]. Temperatures are extreme; June has an average high of 97 degrees F (36 deg C), January averages a high of 56 degrees F (13 deg C). Temperatures exceeding 89 degrees F (32 deg C) can occur on 115 or more days in a year, but temperatures can also fall below 32 degrees F (0 deg C) on 66 days [2,22]. SUCCESSIONAL STATUS : Tarbush occurs in the desert shrub ecosystem, a system which may fall outside traditional ideas of succession. Extreme events or "disturbances" of the classical deciduous forest model of succession do not necessarily produces changes in species composition in the desert. The desert may be "autosuccessional" in this regard. In addition, if species composition does change, no predictable sequence of successional events can be made. The concept of climax as the final phase in a predictable, relatively unidirectional sequence of change in species composition may not be a valid element of desert succession [32]. Disturbance, even to the point of total destruction of aboveground vegetation, does not drastically alter soil or water conditions in the desert. The "climax" or stable vegetation type is well adapted to the extremes of desert climate whether a site is bare or vegetated, unlike mesic counterparts. However, if long-term disturbance has led to species composition change, this may not be reversed by a simple cessation of disturbance. Reinvasion by species of the original community may necessitate unusual and extreme conditions. Because the pace of regrowth is slow in deserts, successional stages may appear to occur, but these may not be necessary for establishment of the stable community that will emerge over time [19]. Campbell [6] considered tarbush to be characteristic of the late seral stage on clay soils and of climax on gravelly clay loams in southern New Mexico. Muller [21] stated that no seral stages occurred in creosotebush-tarbush climax types since disturbance did not result in invasion of new species. Such communities did not develop along classical successional lines. Tarbush is part of the desert grassland disclimax in which shrubs invade the herbaceous community following grazing. Tarbush primarily invades tobosa grasslands. Quickly reinvading, this shrub frustrates attempts to convert such rangeland back to grassland [22,27]. SEASONAL DEVELOPMENT : Tarbush is a rather unusual desert shrub because new growth occurs in midsummer and flowers appear in late fall. Fruit matures from January to March [26].

FIRE ECOLOGY

SPECIES: Flourensia cernua | Tarbush
FIRE ECOLOGY OR ADAPTATIONS : Very little has been published on the effects of fire on tarbush. In general the open zones and low herbaceous cover in tarbush communities prevent hot fires unless there is a year of exceptional winter rains resutling in a heavy stand of annuals to serve as fuels [14]. POSTFIRE REGENERATION STRATEGY : off-site colonizer; seed carried by wind; postfire years one and two

FIRE EFFECTS

SPECIES: Flourensia cernua | Tarbush
IMMEDIATE FIRE EFFECT ON PLANT : Killing fires rarely occur in desert communities because of low fuel loads [14]. However, when such fires do occur, the effect on ecosystem may be extreme because of the harsh environment and low rate of productivity [14]. Little is known about specific fire effects on tarbush. DISCUSSION AND QUALIFICATION OF FIRE EFFECT : NO-ENTRY PLANT RESPONSE TO FIRE : NO-ENTRY DISCUSSION AND QUALIFICATION OF PLANT RESPONSE : NO-ENTRY FIRE MANAGEMENT CONSIDERATIONS : Although their study site did not include tarbush, Rogers and Steele [25] recommended a conservative view toward fire management in deserts in general because of slow recovery rates in such communities.

REFERENCES

SPECIES: Flourensia cernua | Tarbush
REFERENCES : 1. Anderson, D. M. 1988. Seasonal stocking of tobosa managed under continuous and rotation grazing. Journal of Range Management. 41(1): 78-83. [2878] 2. Barbour, Michael G. 1968. Germination requirements of the desert shrub Larrea divaricata. Ecology. 49: 915-923. [4212] 3. Bernard, Stephen R.; Brown, Kenneth F. 1977. Distribution of mammals, reptiles, and amphibians by BLM physiographic regions and A.W. Kuchler's associations for the eleven western states. Tech. Note 301. Denver, CO: U.S. Department of the Interior, Bureau of Land Management. 169 p. [434] 4. Brown, David E. 1982. Chihuahuan desertscrub. In: Brown, David E., ed. Biotic communities of the American Southwest--United States and Mexico. Desert Plants. 4(1-4): 169-179. [3607] 5. Buffington, Lee C.; Herbel, Carlton H. 1965. Vegetational changes on a semidesert grassland range from 1858 to 1963. Ecological Monographs. 35: 139-164. [3383] 6. Campbell, R. S. 1931. Plant succession and grazing capacity on clay soils in southern New Mexico. Journal of Agricultural Research. 43(12): 1027-1051. [4035] 7. Chew, Robert M.; Chew, Alice Eastlake. 1965. The primary productivity of a desert-shrub (Larrea tridentata) community. Ecological Monographs. 35: 355-375. [4254] 8. Correll, Donovan S.; Johnston, Marshall C. 1970. Manual of the vascular plants of Texas. Renner, TX: Texas Research Foundation. 1881 p. [4003] 9. DeLoach, C. Jack; Boldt, Paul E.; Cjordo, Hugo A.; [and others]. 1986. Weeds common to Mexican and U.S. rangelands: proposals for biological control and ecological studies. In: Patton, David R.; Gonzales V., Carlos E.; Medina, Alvin L.; [and others], technical coordinators. Management and utilization of arid land plants: Symposium proceedings; 1985 February 18-22; Saltillo, Mexico. Gen. Tech. Rep. RM-135. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Forest and Range Experiment Station: 49-68. [776] 10. Dollahite, J. W.; Allen, T. J. 1975. The toxicity of the fruit of Flourensia cernua (tarbush) (blackbrush). Southwestern Veterinarian. 28(2): 113-117. [4323] 11. Emmerich, W. E.; Helmer, J. D.; Renard, K. G.; Lane, L. J. 1984. Fate and effectiveness of tebuthiuron applied to a rangeland watershed. Journal of Environmental Quality. 13(3): 382-386. [3969] 12. Gay, Charles W., Jr.; Dwyer, Don D. 1965. New Mexico range plants. Circular 374. Las Cruces, NM: New Mexico State University, Cooperative Extension Service. 85 p. [4039] 13. Herbel, Carlton H.; Abernathy, George H.; Yarbrough, Clyde C.; Gardner, David K. 1973. Rootplowing and seeding arid rangelands in the Southwest. Journal of Range Management. 26(3): 193-197. [4189] 14. Humphrey, Robert R. 1974. Fire in the deserts and desert grassland of North America. In: Kozlowski, T. T.; Ahlgren, C. E., eds. Fire and ecosystems. New York: Academic Press: 365-400. [1217] 15. Kearney, Thomas H.; Peebles, Robert H. 1942. Flourensia. Tarbush, varnishbush. In: Misc. Publ. 423. Flowering plants and ferns of Arizona. Washington, DC: U.S. Department of Agriculture: 957. [3932] 16. Kingsbury, John M. 1964. Poisonous plants of the United States and Canada. Englewood Cliffs, NJ: Prentice-Hall, Inc. 626 p. [122] 17. Krochmal, A.; Paur, S.; Duisberg, P. 1954. Useful native plants in the American Southwestern deserts. Economic Botany. 8: 3-20. [2766] 18. Kuchler, A. W. 1964. Manual to accompany the map of potential vegetation of the conterminous United States. Special Publication No. 36. New York: American Geographical Society. 77 p. [1384] 19. Lathrop, Earl W.; Rowlands, Peter G. 1983. Plant ecology in deserts: an overview. In: Webb, R. H.; Wilshire, H. G, eds. Environmental effects of off-road vehicles. New York: Springer-Verlag: 113-152. [5133] 20. MacMahon, James A. 1985. The Audubon Society nature guides: Deserts. New York: Alfred A. Knopf, Inc. 638 p. [4956] 21. Muller, Cornelius H. 1940. Plant succession in the Larrea-Flourensia climax. Ecology. 21: 206-212. [4244] 22. Paulsen, Harold A., Jr.; Ares, Fred N. 1962. Grazing values and management of black grama and tobosa grasslands and associated shrub ranges of the Southwest. Tech. Bull. No. 1270. Washington, DC: U.S. Department of Agriculture, Forest Service. 56 p. [4041] 23. Peterson, David K.; Whitford, Walter G. 1987. Foraging behavior of Uta stansburiana and Cnemidophorus tigris in two different habitats. Southwestern Naturalist. 32(4): 427-433. [2919] 24. Raunkiaer, C. 1934. The life forms of plants and statistical plant geography. Oxford: Clarendon Press. 632 p. [2843] 25. Thomas, Renee L.; Anderson, Roger C. 1993. Influence of topography on stand composition in a midwestern ravine forest. American Midland Naturalist. 130(1): 1-12. [1742] 26. Stubbendieck, J.; Hatch, Stephan L.; Hirsch, Kathie J. 1986. North American range plants. 3rd ed. Lincoln, NE: University of Nebraska Press. 465 p. [2270] 27. Tueller, Paul T. 1976. Secondary succession, disclimax, and range condition standards in desert scrub vegetation. In: Hyder, D. N., ed. Arid shrublands--Proceedings of the third workshop of the United States/Australia rangelands panel; 1973 March 26 - April 5; Tucson, AZ. Denver, CO: Society for Range Management: 57-65. [3790] 28. U.S. Department of Agriculture, Forest Service. 1937. Range plant handbook. Washington, DC. 532 p. [2387] 29. U.S. Department of Agriculture, Soil Conservation Service. 1982. National list of scientific plant names. Vol. 1. List of plant names. SCS-TP-159. Washington, DC. 416 p. [11573] 30. Weltz, M. A.; Renard, K. G.; Simanton, J. R. 1987. Revised universal soil loss equation for western rangelands. In: Aldon, Earl F.; Gonzales Vicente, Carlos E.; Moir, William H., technical coordinators. Strategies for classification and management of native vegetation for food production in arid zones: Proceedings; 1987 October 12-16; Tucson, AZ. Gen. Tech. Rep. RM-150. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Forest and Range Experiment Station: 104-111. [2730] 31. Wondzell, Steven M.; Cunningham, Gary L.; Bachelet, Dominique. 1987. A hierarchical classification of landforms: some implications for understanding local and regional vegetation dynamics. In: Aldon, Earl F.; Gonzales Vicente, Carlos E.; Moir, William H., technical coordinators. Strategies for classification and management of native vegetation for food production in arid zones; 1987 October 12-16; Tucson, AZ. Gen. Tech. Rep. RM-150. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Forest and Range Experiment Station: 15-23. [2727] 32. Zedler, Paul H. 1981. Vegetation change in chaparral and desert communities in San Diego County, California. In: West, D. C.; Shugart, H. H.; Botkin, D. B., eds. Forest succession: Concepts and application. New York: Springer-Verlag: 406-430. [4241]

Index

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