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Introductory

SPECIES: Arctostaphylos patula | Greenleaf Manzanita
ABBREVIATION : ARCPAT SYNONYMS : NO-ENTRY SCS PLANT CODE : ARPA6 COMMON NAMES : greenleaf manzanita buckbrush. indian tobacco TAXONOMY : The currently accepted scientific name of greenleaf manzanita is Arctostaphylos patula Greene [60,84]. There are no infrataxa [84]. Hybrids resulting from crsses between greenleaf manzanita and other Arctostaphylos species include: A. X coloradensis Rollins - a hybrid of A. uva-ursi x A. patula [71] A. X jepsonii Eastwood - a hybrid of A. patula Greene x A. viscidia ssp. mariposa Dudley var. bivisa Jepsson [21,69]. LIFE FORM : Shrub FEDERAL LEGAL STATUS : No special status OTHER STATUS : MT State Rank: S1 - critically imperiled in Montana (5 or fewer occurrences) [50]. Global Rank: G5 - demonstrably secure globally [50]. COMPILED BY AND DATE : Mary Lou Zimmerman, April 1991 LAST REVISED BY AND DATE : NO-ENTRY AUTHORSHIP AND CITATION : Zimmerman, Mary Lou. 1991. Arctostaphylos patula. In: Remainder of Citation

DISTRIBUTION AND OCCURRENCE

SPECIES: Arctostaphylos patula | Greenleaf Manzanita
GENERAL DISTRIBUTION : Greenleaf manzanita is the most common manzanita in the Great Basin and much of the Sierra Nevada [43,59]. From the Great Basin it ranges north through the Oregon Cascades to Klickitat County, Washington [22]; east to western Colorado [21]; south to the higher elevations of northern Arizona [31]; and west through the Sierra Nevada to the Coast Ranges of California north of Lake County [44]. There is also an isolated occurrence of this species in Lake County, Montana [13]. ECOSYSTEMS : FRES20 Douglas-fir FRES21 Ponderosa pine FRES23 Fir - spruce FRES26 Lodgepole pine FRES27 Redwood FRES28 Western hardwoods FRES34 Chaparral - mountain shrub FRES35 Pinyon - juniper STATES : AZ CA CO ID MT NV NM OR UT WA WY ADMINISTRATIVE UNITS : CARE BRCA CEBR CRLA DINO GRCA LAVO LABE NABR YOSE ZION BLM PHYSIOGRAPHIC REGIONS : 3 Southern Pacific Border 4 Sierra Mountains 5 Columbia Plateau 6 Upper Basin and Range 7 Lower Basin and Range 9 Middle Rocky Mountains 10 Wyoming Basin 11 Southern Rocky Mountains 12 Colorado Plateau 13 Rocky Mountain Piedmont KUCHLER PLANT ASSOCIATIONS : K005 Mixed conifer forest K007 Red fir forest K008 Lodgepole pine - subalpine forest K010 Ponderosa shrub forest K011 Western ponderosa forest K018 Pine - Douglas-fir forest K019 Arizona pine forest K022 Great Basin pine forest K023 Juniper - pinyon woodland K024 Juniper steppe woodland K029 California mixed evergreen forest K033 Chaparral K034 Montane chaparral SAF COVER TYPES : 207 Red fir 210 Interior Douglas-fir 211 White fir 218 Lodgepole pine 220 Rocky Mountain juniper 237 Interior ponderosa pine 238 Western juniper 239 Pinyon - juniper 243 Sierra Nevada mixed conifer 244 Pacific ponderosa pine - Douglas-fir 245 Pacific ponderosa pine 247 Jefferey pine 248 Knobcone pine 249 Canyon live oak SRM (RANGELAND) COVER TYPES : NO-ENTRY HABITAT TYPES AND PLANT COMMUNITIES : Greenleaf manzanita is indicative of open areas having dry, well-drained, coarse soils, poor site index, and a history of fire [21,43,44,74]. Greenleaf manzanita is listed as a dominant, codominant, or indicator species in the following publications: Plant communities and habitat types in the Lava Beds National Monument, California [14] Natural vegetation of Oregon and Washington [83] Coniferous forest habitat types of northern Utah [40] Montane and subalpine forests of the Transverse and Peninsular ranges [56] Ponderosa pine habitat types as an indicator of site quality in the Dixie National Forest, Utah [63] Plant associations of the central Oregon Pumice Zone [64] Coniferous forest habitat types of central and southern Utah [74]

VALUE AND USE

SPECIES: Arctostaphylos patula | Greenleaf Manzanita
WOOD PRODUCTS VALUE : A 1986 study describes the feasibility of using greenleaf manzanita and Parry manzanita (Arctostaphylos manzanita) as raw material for processing into products such as torula yeast, furfural, methanol, brewer's yeast, and other assorted sugars and acids. These products were obtained through hydrolysis of various wood components [6]. IMPORTANCE TO LIVESTOCK AND WILDLIFE : Greenleaf manzanita is virtually worthless to livestock as browse [43,49]. Even domestic goats only browsed this shrub when nothing preferable was available [49,59]. Greenleaf manzanita is of considerable value as a food source for wildlife. Mature berries are eaten by bear, grouse, turkey, and song birds [59]. Use of the foliage as browse by deer is ample in the fall, winter, and spring [39]. Deer also browse sprouts and seedlings [49]. Both livestock and deer prefer the tender young shoots and seedlings common the first couple of years following fire to the mature foliage [49]. PALATABILITY : The palatability of greenleaf manzanita is listed as poor for cattle, sheep, and horses. It ranges from fair to good for various wildlife species. The degree of use shown by livestock and wildlife species for greenleaf manzanita in Colorado, Utah, and California is rated as follows [12,49]: CO UT CA Cattle ---- Poor Poor Sheep ---- Poor Poor Horses ---- Poor Poor Elk Fair Poor ---- Mule deer Good Poor Good Small mammals Good Good ---- Small nongame birds Good Fair ---- Upland game birds Good Fair ---- Waterfowl ---- Poor ---- NUTRITIONAL VALUE : No species of manzanita provides high quality browse [49]. The percentage of crude protein of browse material of greenleaf manzanita is relatively low year-round, ranging from 5.2 to 7.8 percent [4]. COVER VALUE : Chaparral generally harbors numerous species of seed-eating birds and rodents [51]. The value of greenleaf manzanita as cover for small mammals and birds is good, but for large mammals is poor. The degree to which greenleaf manzanita provides environmental protection during one or more seasons for wildlife species in Colorado and Utah is as follows [12]: CO UT Elk Poor Poor Mule deer Poor Poor Small mammals Good Good Small nongame birds Good Good Upland game birds Fair Fair Waterfowl ---- Poor VALUE FOR REHABILITATION OF DISTURBED SITES : Because of its ability to resprout quickly from the lignotuber (as little as 10 days to 3 weeks), this is an important species for rehabilitating disturbed sites, especially burned areas [3,43,59]. The shrub forms a good ground cover, and through the addition of humus tends to improve the site [51,59]. Seeds of this species are produced annually in large quantities and lie dormant in the soil [30,51,68]. These seeds will not germinate until exposed to heat from fire or unless they are otherwise mechanically scarified [43,51,53,66]. Seedling establishment is dependent upon seed production prior to fire, protection during fire, microsite characteristics, and postfire weather [24]. Greenleaf manzanita is listed as a superior shrub species for erosion control on sites in the Tahoe Basin of California [52]. OTHER USES AND VALUES : Food: Native peoples of the Great Basin ate the fruits occasionally and made an extract from the leaves for use as a diuretic [43]. They also made cider from the ripe fruits [59]. The berries can be made into jelly, and the seeds can be ground into flour [43]. Landscaping: The shrub is recommended for use in native and dryland landscaping in California [3]. Livestock barrier: Using brush fields of this shrub as natural fencing is suggested as a method to prevent the unwanted free movement of cattle on open range. Unless special trails are built and maintained within the brush, the cattle are not able to move through it [59]. Watersheds: This shrub is an important cover for many critical watersheds, especially in California [59]. MANAGEMENT CONSIDERATIONS : Timber management: Timber concerns related to the competition of greenleaf manzanita with regeneration of desirable tree species are as follows: Douglas-fir (Pseudotsuga menziesii) - A recent study showed that the uncontrolled development of canyon live oak (Quercus chrysolepis) and greenleaf manzanita sprouts following site preparation caused a significant reduction in Douglas-fir seedling growth. Growth of Douglas-fir seedlings was enhanced by the removal of these sprouts. Management practices that allow the development of even moderate levels of sprout competition with newly planted seedlings will substantially lengthen the rotation age of the stand [25,54]. The leaves of greenleaf mazanita have shown allelopathic qualities that have the potential to contribute to slow regeneration of managed stands of Douglas-fir in southern Oregon [57]. Ponderosa pine (Pinus ponderosa) - The growth of ponderosa pine seedlings is severely limited by the presence of sprouting greenleaf manzanita shrubs. The decline in growth is due to root competition for water. A greenleaf manzanita crown density of only 25 percent of the total cover resulted in a nearly 60 percent loss in tree productivity [47]. Established tree seedlings seldom die from the suppressing effects of the competing vegetation, but the growth loss could be substantial. Shrub crown cover of greater than 30 percent can cause significant growth loss, and rotations can be lengthened from 1 to 20 years [42]. Sugar pine (Pinus lambertiana) - The growth of sugar pine seedlings is severely retarded by the presence of greenleaf manzanita in the overstory; only 18 percent will survive in the understory over an 18- to 24-year period. However, sugar pine seedlings will compete if given an even start with shrub seedlings [37]. Brewer spruce (Picea breweriana) - The seedlings of Brewer spruce can establish under greenleaf manzanita shrubs. They have the ability to grow well despite competition for soil moisture and light [55]. Control treatments: The application of herbicides such as 2,4,D; 2,4,5-T; 2,4,DB; and Triclopyr ester have been proven effective in controlling greenleaf manzanita [7,9,17,46,61]. The nonsprouting form of this shrub is particularly vulnerable to herbicidal treatment [17,61]. The sprouting form may be more persistent and require more frequent applications of higher concentration herbicides carried in oil emulsions rather than water [17,61]. Mechanical treatments, such as slashing, disking, brushraking, and controlled burning (when done in open areas, not in the forest understory), were ineffective as a means of hrub control when applied alone. This is due to the sprouting ability of root burls, and the presence of viable seeds in the soil [38,54].

BOTANICAL AND ECOLOGICAL CHARACTERISTICS

SPECIES: Arctostaphylos patula | Greenleaf Manzanita
GENERAL BOTANICAL CHARACTERISTICS : Greenleaf manzanita is an erect native perennial shrub, approximately 3 to 7 feet (1-2 m) tall. Its limbs are crooked, many branched, stout, and rigid. The twigs are covered with fine hairs. The bark is smooth, shiny, and reddish brown. On older stems the bark becomes "shreddy". Stripping occurs and exposes the light colored whitish-green wood underneath. Those stems that are stripped of their bark become especially twisted and gnarled. The evergreen leaves are bright green to yellow-green, simple, alternate, leathery, broadly oval, hairless, entire, and have distinct petioles. The pinkish flowers are borne on nodding terminal clusters. The petals are fused together in an urn shape. The manzanita fruit is a berrylike drupe that looks like a small apple. It is dark reddish-brown to black and has a thin mealy pulp enclosing 4 to 10 stony seeds. The seeds may be separate or variously coalesced [3,26,43,44,49,59,69]. Greenleaf manzanita has a heavy, turnip-shaped or globular lignotuber which may include a tabular platform [24,26,76]. Its roots generally reach 10 feet (3 m) or more in depth [24]. Stands of greenleaf manzanita may reach 20 to 100 hundred years of age [20,32,58]. Lignotuber age is rarely documented. It is difficult to determine the age of a burl by its annual rings because the wood tissue is swirled and arranged in an irregular pattern. Carbon-dating techniques have shown that burls may persist in some species of chaparral brush for 200 hundred years or more [24]. RAUNKIAER LIFE FORM : Phanerophyte REGENERATION PROCESSES : Sexual: Greenleaf manzanita reproduces sexually by seed. These seeds have an extremely thick endocarp and will not germinate unless scarified. Seed coat scarification may occur naturally by the high temperatures associated with fire, mechanically by soil disturbances, such as those associated with logging activities, or chemically [3,28,51]. A recent laboratory study suggested that exposure to light inhibited the germination of greenleaf manzanita seeds [35]. Seeds stored in the soil appear to have a great longevity as evidenced by the synchronous establishment of large numbers of seedlings after fire in 400-year-old forests [36]. Seed longevity is also illustrated by the fact that there is little difference in the number of seedlings after fires in 100-year-old stands of chaparral than after fires in 20-year-old stands [32]. Greenleaf manzanita produces heavy seed crops nearly every year ( 10,000 seeds per acre [24,710 seeds/ha]) [51]. These seeds can tolerate soil temperatures in excess of 200 degrees F (93 degrees C) [66]. Animals are the primary mode of seed dispersal [41]. Insects are primarily responsible for the pollination of greenleaf manzanita flowers [41]. The flowers occurring on one individual are usually noncompatible [43]. Outcrossing and hybridization are common within this species [2,24]. Vegetative: Greenleaf manzanita regenerates vegetatively through sprouting and layering. Sprouting occurs from dormant buds located within the root burl or lignotuber [75]. These buds are stimulated to sprout after the removal of the aboveground crown [23,24,43,51]. This type of new growth occurs rather rapidly and may be observed in as little as 10 days to 3 weeks [23,24,43]. Greenleaf manzanita is generally able to sprout when the plant reaches approximately 2 years of age, as it takes about this long for the root burl to fully develop [24]. Fire may promote an increase in the size of the root burl [26]. Forma platyphylla does not have a root burl and is not able to sprout [71]. Layering may occur when manzanita branches are forced to the ground and kept there for long periods of time, such as may occur with a heavy snowfall. Under conditions such as these, the branches may sprout roots and develop into separate plants [24,43,69]. SITE CHARACTERISTICS : Greenleaf manzanita is typically found on dry sites. It characteristically grows in full sunlight on well-drained soils. It is found in the openings of coniferous forests, on old burns, and in arid chaparral belts [59]. It is found on a variety of aspects and at elevations ranging between 3,100 and 10,000 feet (945 and 3,048 m) throughout its range [1,5,11,40,56,64,74]. Soil: Greenleaf manzanita typically occurs on soils that are well-drained, shallow to moderately deep, and sandy loam to silty loam in texture. Parent materials may include sandstones, limestones, and granite types [5,11,40,64,74]. In Utah greenleaf manzanita shows a preference for acidic and saline soils over sodic-saline and organic soils [12]. Climate: Greeenleaf manzanita usually occurs within warm, dry, semiarid climes [5,40,56,74]. Elevation: Elevational ranges for greenleaf manzanita in several western locations follow: Location Elevation Reference w Colorado 7,500 to 9,000 feet (2,286-2,743 m) [59] Utah 3,700 to 10,000 feet (1,128-3,048 m) [12,40,72] n Arizona 7,000 to 8,500 feet (2,134-2,591 m) [31] Sierra Nevada 2,500 to 9,000 feet ( 762-2,743 m) [59] SUCCESSIONAL STATUS : Facultative Seral Species Greenleaf manzanita-dominated communities have been variously referred to as grassland climax, true climax, pyric climax, and transitional vegetation [19,51]. Greenleaf manzanita displays characteristics common to shade intolerant pioneer species [73,59]. It begins to die back when overtopped by trees, preferring open areas in full sunlight [53]. It is often one of the first plants to become established on disturbed sites, especially after fire [59]. When this plant occurs in locations susceptible to frequent fires, it has the ability to regenerate quickly, allowing it to perpetually dominate a site [8,59,65,73]. On sites where fire is excluded for long periods of time, greenleaf manzanita may provide a better microclimate for some tree seedlings than would exist on harsh sites in full sunlight, and it may enhance soil conditions through the addition of organic material [51]. This would allow for the relatively slow but sure establishment of the seedlings of some species of pine. Several authors have noted that conifers may regain site dominance from chaparral within 10 to 30 years [51]. SEASONAL DEVELOPMENT : Greenleaf manzanita flowers from late March to June, depending on location [59]. In California flowering occurs from April to June [44,49], in the Great Basin from May to June [43]. Flowering of this species may be triggered by summer moisture stress [3]. The number of flowers produced by a shrub is dependent upon the amount of the previous year's precipitation. The flower buds form 1 year prior to the time they mature. They are dormant the following summer, fall, and winter, and bloom the next spring [43]. The fruits ripen in late summer to early fall [59]. Generally, this species fruits over its entire range between July and October [3,67]. In Nevada, fruiting occurs from May to September [67]. The fruits may occasionally persist on the shrub year-round [62]. The seeds are generally dispersed in the summer and fall [3,34]. Most chaparral species experience the greatest amount of growth in May and June. Growth ceases in mid-July, due to high air temperatures and low soil-moisture [24].

FIRE ECOLOGY

SPECIES: Arctostaphylos patula | Greenleaf Manzanita
FIRE ECOLOGY OR ADAPTATIONS : Greenleaf manzanita has a dynamic relationship with fire [18]. This shrub has adapted specialized reproductive processes that enhance its ability to survive fires [36]. It can reestablish by sprouting from dormant buds in the root burl or from fire-stimulated germination of dormant residual seeds in the soil [36,59,66]. Greenleaf manzanita is very susceptible to fire due to its stand density, presence of volatile materials in its leaves, low moisture content of foliage during summer, and the persistence of its dead branches and stems [10,18,51]. This shrub forms stands that are conducive to very rapid and extensive fire spread due to its physical and chemical characteristics [33]. POSTFIRE REGENERATION STRATEGY : Small shrub, adventitious-bud root crown Ground residual colonizer (on-site, initial community)

FIRE EFFECTS

SPECIES: Arctostaphylos patula | Greenleaf Manzanita
IMMEDIATE FIRE EFFECT ON PLANT : Fire generally top-kills greenleaf manzanita, but severe fire may kill it completely. Fire generally scarifies the seed, which promotes later germination [32,33,35]. DISCUSSION AND QUALIFICATION OF FIRE EFFECT : The seeds of greenleaf manzanita can survive temperatures in excess of 200 degrees Fahrenheit (93 deg C) for 40 minutes and still germinate [66]. PLANT RESPONSE TO FIRE : Fire stimulates greenleaf manzanita seeds stored in the soil to germinate [15,28,36,59,68]. Germination of these seeds occurs in the 1st postfire year [36]. It may take 10 or more years before these seedlings mature and produce a significant seed crop [33]. Unless the entire periphery of the lignotuber is deeply charred, which seldom occurs, vigorous sprouting occurs following fire [48]. Shrubs produce new sprouts from dormant buds in the lignotuber in as little as 10 days to 3 weeks [23,24,43]. These new sprouts are capable of heavy seed production by the 2nd postfire year [33]. DISCUSSION AND QUALIFICATION OF PLANT RESPONSE : Weatherspoon [68] reported on the effects of preharvest burning for shrub control in a white fir (Abies concolor var. lowiana) stand in California. The density of greenleaf manzanita seedlings after postharvest burning was considerably higher for spring burns than for fall burns. This seasonal difference was attributable to consistently higher percent burned area in spring than in fall; in the fall burning period the available fuels were wet due to rains. The density of greenleaf manzanita seedlings was not significantly reduced by preharvest burning. This may have been due to the relatively low fuel-consuption levels in these burns [68]. FIRE MANAGEMENT CONSIDERATIONS : An understanding of the dynamics of shrub reestablishment after fire is an important fire management concern. This is dependent upon an understanding of shrub reproductive strategies [33]. When fire is used for brush control, consumption level, as well as shrub phenology, is an important factor contributing to mortality. Phenologically, shrubs are more resistant to fire in fall, but more fuels are generally available for consumption at this time. Therefore, more destructive heat can be generated around meristematic tissues and root crowns [28]. It has been reported that the greatest mortality of shrubs occurred during high consumption burns regardless of season, and that burning during the active aboveground growing season appeared to increase mortality regardless of the amount of duff consumed. Timing controlled burns to coincide with dryer fuel conditions and active aboveground growth may result in the highest mortality rates [29]. Fire can also be used to reduce or eliminate the greatly increased fire hazard of the standing dead brush, to set back resprouting brush a second time, and to remove the impenetrable mass of dead brush resulting from herbicide application [15]. Prescribed burning in the early spring, before active shrub growth, can be used to increase palatability of foliage to wildlife [29]. Studies indicate that prescribed understory burning can used successfully to kill or reduce the vigor of greenleaf manzanita shrubs and seedlings, deplete the amount of viable residual seed in the soil, and thus prepare a better seedbed for pine and white fir (Abies concolor) regeneration [28,68]. An increase in understory slash depth may reduce the density of manzanita seedlings [68].

REFERENCES

SPECIES: Arctostaphylos patula | Greenleaf Manzanita
REFERENCES : 1. Ball, Charles T.; Keeley, Jon; Mooney, Harold; [and others]. 1983. Relationship between form, function, and distribution of two Arctostaphylos species (Ericaceae) and their putative hybrids. Oecologia Plantarum. 4: 153-164. [12179] 2. Barbour, Michael G.; Billings, William Dwight, eds. 1988. North American terrestrial vegetation. Cambridge; New York: Cambridge University Press. 434 p. [13876] 3. Berg, Arthur R. 1974. Arctostaphylos Adans. manzanita. In: Schopmeyer, C. S., technical coordinator. Seeds of woody plants in the United States. Agric. Handb. 450. Washington, DC: U.S. Department of Agriculture, Forest Service: 228-231. [7428] 4. Bissell, Harold D.; Strong, Helen. 1955. The crude protein variations in the browse diet of California deer. California Fish and Game. 41(2): 145-155. [10524] 5. Blackburn, Wilbert H.; Tueller, Paul T.; Eckert, Richard E., Jr. 1969. Vegetation and soils of the Pine and Mathews Canyon watersheds. Reno, NV: University of Nevada, Agricultural Experiment Station. 109 p. In cooperation with: U.S. Department of the Interior, Bureau of Land Management. [7437] 6. Brink, D. L.; Merriman, M. M.; Gullekson, E. E. 1987. Ethanol fuel, organic chemicals, single-cell proteins: a new forest products industry. In: Plumb, Timothy R.; Pillsbury, Norman H., technical coordinators. Proceedings of the symposium on multiple-use management of California's hardwood resources; 1986 November 12-14; San Luis Obispo, CA. Gen. Tech. Rep. PSW-100. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 237-243. [5379] 7. Burrill, Larry C.; Braunworth, William S., Jr.; William, Ray D.; [and others], compilers. 1989. Pacific Northwest weed control handbook. Corvallis, OR: Oregon State University, Extension Service, Agricultural Communications. 276 p. [6235] 8. Clements, Frederic E. 1936. Nature and structure of the climax. Journal of Ecology. 24: 252-284. [11729] 9. Conard, Susan G.; Emmingham, W. H. 1984. Herbicides for forest brush control in southwestern Oregon. Corvallis, OR: Oregon State University, College of Forestry. 7 p. [10817] 10. Countryman, Clive M. 1982. Physical characteristics of some northern California brush fuels. Gen. Tech. Rep. PSW-61. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station. 8 p. [4177] 11. Dealy, J. Edward. 1971. Habitat characteristics of the Silver Lake mule deer range. Res. Pap. PNW-125. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station. 99 p. [782] 12. Dittberner, Phillip L.; Olson, Michael R. 1983. The plant information network (PIN) data base: Colorado, Montana, North Dakota, Utah, and Wyoming. FWS/OBS-83/86. Washington, DC: U.S. Department of the Interior, Fish and Wildlife Service. 786 p. [806] 13. Dorn, Robert D. 1984. Vascular plants of Montana. Cheyenne, WY: Mountain West Publishing. 276 p. [819] 14. Erhard, Dean H. 1979. Plant communities and habitat types in the Lava Beds National Monument, California. Corvallis, OR: Oregon State University. 173 p. Thesis. [869] 15. Gratkowski, H. 1961. Brush seedlings after controlled burning of brushlands in southwestern Oregon. Journal of Forestry. 59(12): 885-888. [3392] 16. Gratkowski, H. 1975. Silvicultural use of herbicides in Pacific Northwest forests. Gen. Tech. Rep. PNW-37. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station. 44 p. [10998] 17. Gratkowski, H. 1978. Herbicides for shrub and weed control in western Oregon. Gen. Tech. Rep. PNW-77. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station. 48 p. [6539] 18. Hanes, Ted L. 1974. The vegetation called chaparral. In: Rosenthal, Murray, ed. Symposium on living with the chaparral: Proceedings; 1973 March 30-31; Riverside, CA. San Francisco, CA: The Sierra Club: 1-5. [3261] 19. Hanes, Ted L. 1977. California chaparral. In: Barbour, Michael G.; Major, Jack, eds. Terrestrial vegetation of California. New York: John Wiley and Sons: 417-469. [7216] 20. Hanes, Ted L. 1981. California chaparral. In: Di Castri, F.; Goodall, D. W.; Specht, R. L., eds. Mediterranean-type shrublands. Amsterdam: Elsevier Science Publishers B.V: 139-174. [13576] 21. Harrington, H. D. 1964. Manual of the plants of Colorado. 2d ed. Chicago: The Swallow Press Inc. 666 p. [6851] 22. Hitchcock, C. Leo; Cronquist, Arthur. 1973. Flora of the Pacific Northwest. Seattle, WA: University of Washington Press. 730 p. [1168] 23. Hobbs, Stephen D.; Wearstler, Kenneth A., Jr. 1985. Effects of cutting sclerophyll brush on sprout development and Douglas- fir growth. Forestry Ecology and Management. 13: 69-81. [9690] 24. James, Susanne. 1984. Lignotubers and burls--their structure, function and ecological significance in Mediterranean ecosystems. Botanical Review. 50(3): 225-266. [5590] 25. Jaramillo, Annabelle E. 1988. Growth of Douglas-fir in southwestern Oregon after removal of competing vegetation. Res. Note PNW-470. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station. 10 p. [6224] 26. Jepson, Willis L. 1916. Regeneration in Manzanita. Madrono. 1: 3-11. [12206] 27. Kartesz, John T.; Kartesz, Rosemarie. 1980. A synonymized checklist of the vascular flora of the United States, Canada, and Greenland. Volume II: The biota of North America. Chapel Hill, NC: The University of North Carolina Press; in confederation with Anne H. Lindsey and C. Richie Bell, North Carolina Botanical Garden. 500 p. [6954] 28. Kauffman, J. Boone; Martin, R. E. 1985. A preliminary investigation on the feasibility of preharvest prescribed burning for shrub control. In: Proceedings, 6th annual forestry vegetation management conference; [Date of conference unknown]; Redding, CA. [Place of publication unknown]. [Publisher unknown]. 89-114. [7526] 29. Kauffman, J. Boone; Martin, Robert E. 1985. Shrub and hardwood response to prescribed burning with varying season, weather, and fuel moisture. In: Proceedings, 8th conference on fire and forest meteorology; 1985 April 29-May 2; Detroit, MI. Bethesda, MD: Society of American Foresters: 279-286. [9796] 30. Kauffman, J. B.; Martin, R. E. 1990. Sprouting shrub response to different seasons and fuel consumption levels of prescribed fire in Sierra Nevada mixed conifer ecosystems. Forest Science. 36(3): 748-764. [13063] 31. Kearney, Thomas H.; Peebles, Robert H.; Howell, John Thomas; McClintock, Elizabeth. 1960. Arizona flora. 2d ed. Berkeley, CA: University of California Press. 1085 p. [6563] 32. Keeley, Jon E. 1977. 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