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Introductory

SPECIES: Vaccinium uliginosum ssp. occidentale | Western Huckleberry
ABBREVIATION : VACULIO SYNONYMS : Vaccinium occidentale Gray [31,49] SCS PLANT CODE : VAULO COMMON NAMES : western huckleberry western bog blueberry westernbog blueberry western blueberry swamp huckleberry swamp blueberry huckleberry TAXONOMY : The currently accepted scientific name of western huckleberry is Vaccinium uliginosum L. ssp. occidentale (Gray) Hulten [51]. LIFE FORM : Shrub FEDERAL LEGAL STATUS : No special status OTHER STATUS : NO-ENTRY COMPILED BY AND DATE : D. Tirmenstein, May 1990 LAST REVISED BY AND DATE : NO-ENTRY AUTHORSHIP AND CITATION : Tirmenstein, D. 1990. Vaccinium uliginosum ssp. occidentale. In: Remainder of Citation

DISTRIBUTION AND OCCURRENCE

SPECIES: Vaccinium uliginosum ssp. occidentale | Western Huckleberry
GENERAL DISTRIBUTION : Western huckleberry grows from Alaska and British Columbia southward through Washington and Oregon to northwestern California [16,22]. Along the Pacific Coast, it occurs mostly east of the Cascades and reaches as far south as the Sierra Nevada of California [16]. It extends northeastward into the Rocky Mountains of Montana, northern Idaho, and Utah [8,31,49]. ECOSYSTEMS : FRES22 Western white pine FRES23 Fir - spruce FRES24 Hemlock - Sitka spruce FRES26 Lodgepole pine FRES44 Alpine STATES : AK CA ID ME MT NY UT WI BC NF ADMINISTRATIVE UNITS : NOCA YELL GLAC CRLA GRTE LAVO MORA YOSE BLM PHYSIOGRAPHIC REGIONS : 2 Cascade Mountains 4 Sierra Mountains 5 Columbia Plateau 8 Northern Rocky Mountains 9 Middle Rocky Mountains KUCHLER PLANT ASSOCIATIONS : K001 Spruce - cedar - hemlock forest K004 Fir - hemlock forest K007 Red fir forest K013 Cedar - hemlock - pine K015 Western spruce - fir forest SAF COVER TYPES : 206 Engelmann spruce - subalpine fir 207 Red fir 211 White fir 213 Grand fir 215 Western white pine 218 Lodgepole pine 224 Western hemlock 225 Western hemlock - Sitka spruce 227 Western redcedar - western hemlock 228 Western redcedar 253 Black spruce - white spruce 254 Black spruce - paper birch 256 California mixed subalpine SRM (RANGELAND) COVER TYPES : NO-ENTRY HABITAT TYPES AND PLANT COMMUNITIES : Western huckleberry grows as an understory dominant in certain moist lodgepole pine (Pinus contorta), subalpine fir (Abies lasiocarpa) and/or Engelmann spruce (Picea engelmannii) forests. In parts of California and the Northwest, it grows with lodgepole pine, red fir (A. magnifica), and white fir (A. concolor) [48]. Western huckleberry is also an important understory shrub in mixed subalpine forests in the Sierra Nevada [40] and is a common component of slow-draining bogs in the northern Sierra Nevada and Klamath Mountains [44]. Shrub communities dominated by western huckleberry often occur in narrow bands or patches in bogs or mesic forest openings. Common codominants in western huckleberry shrub communities include bluejoint reedgrass (Calamagrostis canadensis), Sitka sedge (Carex sitchensis), water sedge (C. aquatilis), few-flowered spikerush (Eleocharis pauciflora), widefruit sedge (C. eurycarpa), tufted hairgrass (Deschampsia cespitosa), and sweetberry honeysuckle (Lonicera caerulea). Published classifications listing western huckleberry as an indicator or dominant species in community types, habitat types, plant associations, or dominance types are presented below. Ecoclass coding system for the Pacific Northwest plant associaitons [12] Riparian dominance types of Monatana [14] Plant association and management guide: Willamette National Forest [15] Riparian zone associations: Deschutes, Ochoco, Fremont, and Winema National Forests [21] Classification and environmental relationships of wetland vegetation in central Yellowstone National Park, Wyoming [28] Wetland community type classification for west-central Montana [34] Riparian classification for the Upper Salmon/Middle Fork Salmon River drainages, Idaho [45] Plant associations of the central Oregon Pumice Zone [48] Plant associates: Common understory associates of western huckleberry include water sedge, blister sedge (C. vesicaria), and other sedges (Carex spp.), tufted hairgrass, bluejoint reedgrass, willows (Salix spp.), bog Labrador tea (Ledum glandulosum), dwarf huckleberry (Vaccinium caespitosum), sweetberry honeysuckle (Lonicera caerulea), bog kalmia (Kalmia polifolia), western azalea (Rhododendron occidentale), thinleaf alder (Alnus incana ssp. tenuifolia), and numerous wetsite forbs [28,37,44,48].

VALUE AND USE

SPECIES: Vaccinium uliginosum ssp. occidentale | Western Huckleberry
WOOD PRODUCTS VALUE : NO-ENTRY IMPORTANCE TO LIVESTOCK AND WILDLIFE : Browse: The young twigs and leaves of western huckleberry provide high quality browse for deer in some locations [30]. Certain lodgepole pine/western huckleberry-forb wetlands of central Oregon are critical habitat for mule deer during spring, summer, and fall [48]. Green foliage of western huckleberry often appears prior to snowmelt [21], and browse may be particularly valuable to deer and elk during the early spring when food is scarce. In other areas it is rarely used by deer or elk in any season [22,28]. The value of western huckleberry browse to domestic sheep and goats ranges between good and poor [30]. In some areas, it is considered fair to good sheep and goat browse, particularly during the fall. Western huckleberry receives some local use by cattle [8,47]. Use of western huckleberry by wildlife and livestock may be limited by its restricted and often rather localized distribution [8]. On particularly wet microsites, it can be used only after the ground dries sufficiently for animals to access the area [8]. Fruit: Berries of western huckleberry are readily eaten by many birds including blue and spruce grouse. Thrushes, towhees, ruffed grouse, and sharp-tailed grouse consume the fruit of many huckleberries (Vaccinium spp.). Mammals such as chipmunks, red fox, gray fox, skunks, and squirrels also feed on huckleberry fruit [27,47]. Berries of western huckleberry are readily eaten by both black and grizzly bears [14] and by many small mammals. PALATABILITY : Palatability of western huckleberry browse is described as low to moderate for deer, elk, and domestic livestock [22]. Mattson [28] reports that it is relatively unpalatable to wild ungulates in the vicinity of Yellowstone National Park. However, Dayton [8] observed that western huckleberry is "one of the more palatable browse species of the genus." Fruit is highly palatable to many birds and mammals. NUTRITIONAL VALUE : Huckleberry (Vaccinium spp.) foliage is relatively high in carotene, manganese, and energy value [7,14]. Huckleberry fruits are sweet and contain high concentrations of both mono- and di-saccharides [42]. Berries are rich in vitamin C and energy content but low in fats [18,36]. COVER VALUE : Western huckleberry provides good cover for a variety of wildlife species. It commonly forms dense thickets beneath lodgepole pine [28], which can serve as favorable nesting, resting, or hiding cover for many smaller birds and mammals. Engelmann spruce/western huckleberry habitat types of western Oregon provide good cover for deer and elk. These sites, which commonly border bogs or marshes, are preferred locations for calving and rearing young [21]. VALUE FOR REHABILITATION OF DISTURBED SITES : Most huckleberries (Vaccinium spp.) can be propagated from hardwood cuttings or from seed. Seedlings grown in the greenhouse can be transplanted onto favorable sites 6 to 7 weeks after emergence. Seed collection and storage techniques have been examined in detail [6]. OTHER USES AND VALUES : Fruits of western huckleberry were traditionally used by many native peoples. Berries of the western huckleberry are eaten fresh, cooked, or made into jams and wine [22]. Berries are sweet and pulpy but rather dry and "of poor quality" compared with the fruit of many other species of Vaccinium [29,41]. Consequently, western huckleberry is not considered to be one of the most important berry producers [29]. Many huckleberries (Vaccinium spp.) have value as ornamentals. Schultz [41] reports western huckleberry-evergreen huckleberry (V. ovatum) hybrids may have horticultural value. MANAGEMENT CONSIDERATIONS : Chemical control: Huckleberries (Vaccinium spp.) exhibit variable susceptibility to herbicides such as 2,4-D, 2,4,5-T, glyphosate, karbutilate, and picloram [2]. Wildlife considerations: Huckleberries are an extremely important food source for grizzly bears [26] and both black and grizzly bears typically exploit areas with dense concentrations of berries. The habitat value of huckleberry shrubfields to grizzly bears can be increased by permanent or at least seasonal road closures, by coordinating timber harvest dates to have minimal impact on habitat use patterns, and by considering the cumulative effects of habitat modification across a broad area. In general, site preparation should include minimizing soil compaction, using cool broadcast burns rather than hot slash burns, or by eliminating site preparation entirely wherever possible. Grizzly use is favored where hiding cover is retained by treating small, irregular patches instead of large contiguous areas, and by leaving stringers of timber within larger cuts [50]. In many areas, bear-human conflicts are most likely to occur during years of huckleberry crop failure [26,38], as hungry bears come into contact with recreationists or wildland residents. Damage to crops and beehives, and livestock losses also typically increase during poor huckleberry years [38].

BOTANICAL AND ECOLOGICAL CHARACTERISTICS

SPECIES: Vaccinium uliginosum ssp. occidentale | Western Huckleberry
GENERAL BOTANICAL CHARACTERISTICS : Western huckleberry is a branching, erect or low semispreading shrub [22,31,41]. Plants are sometimes compact and decumbent [31] and can form dense, extensive thickets or clones [28,41]. Western huckleberry typically reaches 8 to 36 inches (20-91 cm) in height [8,49]. Twigs are yellow-green, smooth, round, and glabrous [22,29,49]. Small, thin, alternate leaves are oblanceolate to obovate, acute at the base and rounded to obtuse at the apex [16,22,31,49]. Leaves are generally less than one-half as long as broad [17]. Leaves are glaucous bluish-green, and often paler or with a waxy, whitish bloom on the lower surface [29]. Leaves turn a bright red or yellow in the fall [28,30]. The urn-shaped flowers of western huckleberry are pink or white [22,31]. Flowers are generally borne singly or in clusters of two to four in the leaf axils [29,31,41]. Fruit is an ellipsoid or spherical berry 0.16 to 0.2 inch (4-5 mm) thick [16,29,31]. Berries are blue or bluish-black, with a dense, waxy bloom [29,41,49]. Western huckleberry, a cluster-fruited species, can produce 10 to 20 times more fruit than single-fruited species of similar size [29]. Berries are sweet but rather dry, and contain approximately 10 individual seeds [30,41]. Seeds are small, brown, compressed, and "cellular-pitted" [31]. RAUNKIAER LIFE FORM : Phanerophyte Geophyte REGENERATION PROCESSES : Western huckleberry is capable of reproducing through seed or vegetatively through sprouting of rhizomes or "underground stems" [41]. Vegetative regeneration appears to be of primary importance in most species of huckleberries (Vaccinium spp.) that occur in western North America [26]. Seed: Seeds of most huckleberries (Vaccinium spp.) are not dormant and require no pretreatment for germination. Seedlings first emerge in approximately 1 month and continue to emerge for long periods of time in the absence of cold stratification [6]. Schultz [41] reports that western huckleberry "spreads readily by underground stems as well as by seed." However, other researchers report that seedlings of western huckleberries are rarely encountered in the field [26]. Seed banking does not appear to be an important regenerative strategy in western huckleberry. The morphologically and ecologically similar bog bilberry is characterized by seeds of short-viability which are readily destroyed by fire [33]. Where plants are killed by disturbance, reestablishment presumably occurs from off-site seed. Edible berries are widely dispersed by birds [24] and mammals. Vegetative regeneration: Most species of huckleberry regenerate from basal sprouts or underground regenerative structures such as roots or rhizomes [39]. Clones of western huckleberry generally expand through rhizome sprouting even in the absence of disturbance [41]. Rhizome sprouting is also likely where aboveground vegetation has been eliminated but where underground regenerative structures remain undamaged. Basal stem sprouting has also been observed after much of the aboveground portions of the plants have been destroyed by fire [22]. SITE CHARACTERISTICS : Western huckleberry grows well on open, moist, wet, swampy or boggy sites [8,22]. Dense stands often develop on favorable sites such as along the edges of fens, wet meadows, ponds, and streams, and at the drier edges of mountain swamps [28,29,41,43]. Since its presence is largely restricted to moist sites, extensive thickets may be common [28,41] but somewhat localized [8]. Clinal boundaries between western huckleberry shrub communities and adjacent drier upland types are often quite abrupt [28]. Soil: Huckleberries (Vaccinium spp.) require acidic conditions and can survive on infertile soils which have relatively low amounts of many essential elements [20]. Western huckleberry often grows on sandy loams with a pH of 4.2 to 5.2 [28,30,47]. Soils are wet to saturated, cold, and with "appreciable" amounts of organic matter [28]. Extensive stands of western huckleberry are commonly associated with a high water table [48]. Elevation: In the Pacific Northwest, western huckleberry generally occurs at moderate to moderately high elevations [22]. However, it is generally restricted to the highest elevations in the Great Basin [30]. Generalized elevational range by state has been documented as follows [9,31,49]: from 5,000 to 11,000 feet (1,524-3,355 m) in CA 5,700 to 8,100 feet (1,737-2,469 m) in MT 10,800 to 11,513 feet (3,294-3,294 m) in UT 6,800 to 11,000 feet (2,042-3,355 m) in WY SUCCESSIONAL STATUS : The successional role of western huckleberry is poorly known. Taylor [43] found no definite successional trends in western huckleberry communities which border small ponds in Yellowstone National Park. In parts of western Oregon, western huckleberry forms climax associations with Sitka sedge on poorly drained sites with undulating microtopography [21]. It also codominates climax communities on boggy, poorly drained soils with few-flowered spikerush [22]. Many moist sites dominated by western huckleberry experience disturbances at infrequent intervals and this shrub apparently persists between disturbances. Western huckleberry often assumes prominence during early seral stages if underground regenerative structures remain undamaged. It may become common during the second stage of succession in western redcedar (Thuja plicata)-western hemlock (Tsuga heterophylla)-grand fir (Abies grandis) forests of Idaho following the decline of initial weedy invaders such as fireweed (Epilobium angustifolium). Sprouts of western huckleberry grow rapidly and this shrub can become a prominent component of vegetative communities within 2 to 3 years after disturbance [24]. SEASONAL DEVELOPMENT : Western huckleberry typically flowers in June or July [17]. Fruit ripens in July or August [47]. Seasonal development by geographic location has been documented as follows [9,17,31]: location flowering fruit ripening CA June-July ---- Pacific Northwest June-July ---- UT July ----

FIRE ECOLOGY

SPECIES: Vaccinium uliginosum ssp. occidentale | Western Huckleberry
FIRE ECOLOGY OR ADAPTATIONS : Western huckleberry typically occurs on relatively moist to wet microsites which burn infrequently [22]. Fire intervals for some boggy sites dominated by this shrub have been estimated at 100 to 300 years [22]. Many, if not most, fires occur when the soil is still at least somewhat moist and plants typically resprout from stem bases or from "underground stems" or rhizomes after light to moderate fires [22,41]. However, fires which occur when the flammable peaty soil is dry can damage or destroy underground regenerative structures [21]. Limited seedling establishment may occur from off-site seed transported by various birds and mammals. POSTFIRE REGENERATION STRATEGY : Small shrub, adventitious-bud root crown Rhizomatous shrub, rhizome in soil Initial-offsite colonizer (off-site, initial community)

FIRE EFFECTS

SPECIES: Vaccinium uliginosum ssp. occidentale | Western Huckleberry
IMMEDIATE FIRE EFFECT ON PLANT : Western huckleberry is described as "sensitive" to cool fires [21]. Even low-intensity fires can remove much of the crown [30]. However, portions of the stem base, as well as underground regenerative structures, often survive these light fires [22]. Western huckleberry commonly occurs on peaty soils which are very flammable when dry. Plants are often killed when the peat is deeply burned [21] and underground regenerative structures destroyed by heat. Fire generally destroys the heat-sensitive seeds of closely related huckleberries such as bog bilberry [33]. DISCUSSION AND QUALIFICATION OF FIRE EFFECT : NO-ENTRY PLANT RESPONSE TO FIRE : Vegetative response: Western huckleberry generally sprouts after light to moderate fires [14,21]. Plants may be "naturally pruned" by light fires which consume the crown but which remove little soil or duff [30]. Basal sprouting commonly occurs where stem bases remain relatively undamaged [21,22]. Sprouting from rhizomes or "underground stems" is likely if the crown has been destroyed but underground regenerative structures left intact [41]. Seed: Western huckleberry may occasionally reestablish a site through seed [41]. However, many researchers report that postfire seedling establishment is extremely rare in huckleberries of western North America [26,(P. Stickney, pers. comm. 1990)]. Seeds of closely related species, such as the bog bilberry, are of short viability and are readily killed by heat [33]. Consequently, seed banking does not appear to be an important postfire regenerative strategy. Some seed may be transported from off-site by birds [24] and mammals. Postfire reestablishment: Stem bases often sprout during the first year after fire [21] and the length of time required for vegetative postfire reestablishment is described as "moderate" [22]. Shrubs which develop from resprouts can become prominent within 2 to 3 years after fire [24]. Postfire reestablishment from seed, if it occurs at all, is likely to be slow. DISCUSSION AND QUALIFICATION OF PLANT RESPONSE : NO-ENTRY FIRE MANAGEMENT CONSIDERATIONS : Berry production: Berry production is generally reduced for at least 5 years after fire in most huckleberries (Vaccinium spp.) of western North America. On some sites, berry production may be significantly reduced for 20 to 30 years or more [26]. Wildlife: Evidence suggests that fire suppression may be having an adverse impact on bear habitat in some areas [46,50]. Once productive seral berry fields are now being invaded by conifers. Since plants beneath a forest canopy generally produce few berries, fruit production has been steadily declining [29]. Logging treatments which include severe soil scarification or slash burns may also result in decreased berry availability. Even where timber harvest favors berry production, lack of cover in early years can limit bear use. However, wildfires often create diverse habitat mosaics which incorporate elements of hiding cover and favor bear use [50].

REFERENCES

SPECIES: Vaccinium uliginosum ssp. occidentale | Western Huckleberry
REFERENCES : 1. 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] 2. Bovey, Rodney W. 1977. Response of selected woody plants in the United States to herbicides. Agric. Handb. 493. Washington, DC: U.S. Department of Agriculture, Agricultural Research Service. 101 p. [8899] 3. Camp, W. H. 1942. A survey of the American species of Vaccinium, subgenus Euvaccinium. Brittonia. 4: 205-247. [6950] 4. Camp, W. H. 1942. On the structure of populations in the genus Vaccinium. Brittonia. 4(2): 189-204. [9512] 5. Camp, W. H. 1945. The North American blueberries with notes on other groups of Vacciniaceae. Brittonia. 5(3): 203-275. [9515] 6. Crossley, John A. 1974. Vaccinium L. Blueberry. In: Schopmeyer, C. S., ed. Seeds of woody plants in the United States. Agric. Handb. 450. Washington, DC: U.S. Department of Agriculture, Forest Service: 840-843. [7774] 7. Dahlgreen, Matthew Craig. 1984. Observations on the ecology of Vaccinium membranaceum Dougl. on the southeast slope of the Washington Cascades. Seattle, WA: University of Washington. 120 p. Thesis. [2131] 8. Dayton, William A. 1931. Important western browse plants. Misc. Publ. 101. Washington, DC: U.S. Department of Agriculture. 214 p. [768] 9. 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] 10. Eyre, F. H., ed. 1980. Forest cover types of the United States and Canada. Washington, DC: Society of American Foresters. 148 p. [905] 11. Garrison, George A.; Bjugstad, Ardell J.; Duncan, Don A.; [and others]. 1977. Vegetation and environmental features of forest and range ecosystems. Agric. Handb. 475. Washington, DC: U.S. Department of Agriculture, Forest Service. 68 p. [998] 12. Hall, Frederick C. 1984. Ecoclass coding system for the Pacific Northwest plant associations. R6 Ecol 173-1984. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Region. 83 p. [7650] 13. Hanley, Thomas A.; McKendrick, Jay D. 1983. Seasonal changes in chemical composition and nutritive values of native forages in a spruce-hemlock forests, southeastern Alaska. Res. Pap. PNW-312. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station. 41 p. [8770] 14. Hansen, Paul L.; Chadde, Steve W.; Pfister, Robert D. 1988. Riparian dominance types of Montana. Misc. Publ. No. 49. Missoula, MT: University of Montana, School of Forestry, Montana Forest and Conservation Experiment Station. 411 p. [5660] 15. Hemstrom, Miles A.; Logan, Sheila E.; Pavlat, Warren. 1987. Plant association and management guide: Willamette National Forest. R6-Ecol 257-B-86. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Region. 312 p. [13402] 16. Hitchcock, C. Leo; Cronquist, Arthur. 1973. Flora of the Pacific Northwest. Seattle, WA: University of Washington Press. 730 p. [1168] 17. Hitchcock, C. Leo; Cronquist, Arthur; Ownbey, Marion. 1959. Vascular plants of the Pacific Northwest. Part 4: Ericaceae through Campanulaceae. Seattle, WA: University of Washington Press. 510 p. [1170] 18. Hunn, Eugene S.; Norton, Helen H. 1984. Impact of Mt. St. Helens ashfall on fruit yields of mountain huckleberry Vaccinium membranaceum, important Native American food. Economic Botany. 38(1): 121-127. [9501] 19. Kartesz, John T. 1994. A synonymized checklist of the vascular flora of the United States, Canada, and Greenland. Volume II--thesaurus. 2nd ed. Portland, OR: Timber Press. 816 p. [23878] 20. Korcak, Ronald F. 1988. Nutrition of blueberry and other calcifuges. Horticultural Reviews. 10: 183-227. [9612] 21. Kovalchik, Bernard L. 1987. Riparian zone associations: Deschutes, Ochoco, Fremont, and Winema National Forests. R6 ECOL TP-279-87. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Region. 171 p. [9632] 22. Kovalchik, Bernard L.; Hopkins, William E.; Brunsfeld, Steven J. 1988. Major indicator shrubs and herbs in riparian zones on National Forests of central Oregon. R6-ECOL-TP-005-88. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Region. 159 p. [8995] 23. 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] 24. Larsen, J. A. 1929. Fires and forest succession in the Bitterroot Mountains of northern Idaho. Ecology. 10: 67-76. [6990] 25. Lyon, L. Jack; Stickney, Peter F. 1976. Early vegetal succession following large northern Rocky Mountain wildfires. In: Proceedings, Tall Timbers fire ecology conference and Intermountain Fire Research Council fire and land management symposium; 1974 October 8-10; Missoula, MT. No. 14. Tallahassee, FL: Tall Timbers Research Station: 355-373. [1496] 26. Martin, Patricia A. E. 1979. Productivity and taxonomy of the Vaccinium globulare, V. membranaceum complex in western Montana. Missoula, MT: University of Montana. 136 p. Thesis. [9130] 27. Martin, Alexander C.; Zim, Herbert S.; Nelson, Arnold L. 1951. American wildlife and plants. New York: McGraw-Hill Book Company, Inc. 500 p. [4021] 28. Mattson, David John. 1984. Classification and environmental relationships of wetland vegetation in central Yellowstone National Park, Wyoming. Moscow, ID: University of Idaho. 409 p. Thesis. [7348] 29. O'Rourke, F. L. 1942. The influence of blossom buds on rooting of hardwood cuttings of blueberry. Proceedings American Society for Horticultural Science. 40: 332-334. [8950] 30. Mozingo, Hugh N. 1987. Shrubs of the Great Basin: A natural history. Reno, NV: University of Nevada Press. 342 p. [1702] 31. Munz, Philip A. 1973. A California flora and supplement. Berkeley, CA: University of California Press. 1905 p. [6155] 32. Munz, Philip A. 1974. A flora of southern California. Berkeley, CA: University of California Press. 1086 p. [4924] 33. Parminter, John. 1983. Fire-ecological relationships for the biogeoclimatic zones and subzones of the Fort Nelson Timber Supply Area: summary report. In: Northern Fire Ecology Project: Fort Nelson Timber Supply Area. Victoria, BC: Province of British Columbia, Ministry of Forests. 53 p. [9203] 34. Pierce, John; Johnson, Janet. 1986. Wetland community type classification for west-central Montana. Missoula, MT: U.S. Department of Agriculture, Forest Service, Northern Region, Ecosystem Management Program. 158 p. [Review draft]. [7436] 35. Raunkiaer, C. 1934. The life forms of plants and statistical plant geography. Oxford: Clarendon Press. 632 p. [2843] 36. Reich, Lee. 1988. Backyard blues. Organic Gardening. 35(6): 28-34. [9179] 37. Roach, A. W. 1952. Phytosociology of the Nash Crater lava flows, Linn County, Oregon. Ecological Monographs. 22: 169-193. [8759] 38. Rogers, Lynn. 1976. Effects of mast and berry crop failures on survival, growth, and reproductive success of black bears. Transactions, North American Wildlife Conference. 41: 431-438. [8951] 39. Rowe, J. S.; Scotter, G. W. 1973. Fire in the boreal forest. Quaternary Research. 3: 444-464. [72] 40. Rundel, Philip W.; Parsons, David J.; Gordon, Donald T. 1977. Montane and subalpine vegetation of the Sierra Nevada and Cascade Ranges. In: Barbour, Michael G.; Major, Jack, eds. Terrestrial vegetation of California. New York: John Wiley & Sons: 559-599. [4235] 41. Schultz, Joseph Herbert. 1944. Some cytotaxonomic and germination studies in the genus Vaccinium. Pullman, WA: Washington State University. 115 p. Thesis. [10285] 42. Stiles, Edmund W. 1980. Patterns of fruit presentation and seed dispersal in bird-disseminated woody plants in the Eastern deciduous forest. American Naturalist. 116(5): 670-688. [6508] 43. Taylor, Dale L. 1969. Biotic succession of lodgepole pine forests of fire origin in Yellowstone National Park. Laramie, WY: University of Wyoming. 320 p. M.S. thesis. [9481] 44. Thorne, Robert F. 1977. Montane and subalpine forests of the Transverse and Peninsular ranges. In: Barbour, Michael G.; Major, Jack, eds. Terrestrial vegetation of California. New York: John Wiley and Sons: 537-557. [7214] 45. Tuhy, Joel S.; Jensen, Sherman. 1982. Riparian classification for the Upper Salmon/Middle Fork Salmon River drainages, Idaho. Smithfield, UT: White Horse Associates. Final Report, Contract with U.S.S. Forest Service, Region 4. 153 p. [8380] 46. Unsworth, James W.; Beecham, John J.; Irby, Lynn R. 1989. Female black bear habitat use in west-central Idaho. Journal of Wildlife Management. 53(3): 668-673. [8407] 47. Van Dersal, William R. 1938. Native woody plants of the United States, their erosion-control and wildlife values. Washington, DC: U.S. Department of Agriculture. 362 p. [4240] 48. Volland, Leonard A. 1985. Plant associations of the central Oregon Pumice Zone. Rt-ECOL-104-1985. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Region. 138 p. [7341] 49. Welsh, Stanley L.; Atwood, N. Duane; Goodrich, Sherel; Higgins, Larry C., eds. 1987. A Utah flora. Great Basin Naturalist Memoir No. 9. Provo, UT: Brigham Young University. 894 p. [2944] 50. Zager, Peter Edward. 1980. The influence of logging and wildfire on grizzly bear habitat in northwestern Montana. Missoula, MT: University of Montana. 131 p. Dissertation. [5032] 51. Hickman, James C., ed. 1993. The Jepson manual: Higher plants of California. Berkeley, CA: University of California Press. 1400 p. [21992] 52. Stickney, Peter F. 1989. Seral origin of species originating in northern Rocky Mountain forests. Unpublished draft on file at: U.S. Department of Agriculture, Forest Service, Intermountain Research Station, Fire Sciences Laboratory, Missoula, MT; RWU 4403 files. 7 p. [20090] 53. U.S. Department of Agriculture, Soil Conservation Service. 1994. Plants of the U.S.--alphabetical listing. Washington, DC: U.S. Department of Agriculture, Soil Conservation Service. 954 p. [23104] 54. U.S. Department of the Interior, National Biological Survey. [n.d.]. NP Flora [Data base]. Davis, CA: U.S. Department of the Interior, National Biological Survey. [23119]

Index

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Information Courtesy: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory. Fire Effects Information System

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