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Introductory

WILDLIFE SPECIES: Odocoileus hemionus | Mule Deer
ABBREVIATION : ODHE COMMON NAMES : mule deer burro deer California mule deer Cedros deer Columbian black-tailed deer desert deer Inyo deer peninsula mule deer Rocky Mountain mule deer Sitka black-tailed deer southern mule deer Tiburon deer TAXONOMY : There are 11 subspecies of mule deer in North America. Black-tailed deer, which consist of two mule deer subspecies, comprise a distinct race, differentiated by appearance and behavior [35]. Only seven subspecies are recognized. There is some doubt as to the distribution, differentiation, and possible existence of the remaining four. These four are indicated below with an asterisk [52]: Odocoileus hemionus ssp. hemionus - Rocky Mountain mule deer O. hemionus ssp. crooki - desert mule deer O. hemionus ssp. californicus - California mule deer O. hemionus ssp. fuliginatus - southern mule deer O. hemionus ssp. peninsulae - peninsula mule deer O. hemionus ssp. columbianus - Columbian black-tailed deer O. hemionus ssp. sitkensis - Sitka black-tailed deer O. hemionus ssp. eremicus* - burro deer O. hemionus ssp. sheldoni* - Tiburon Island mule deer O. hemionus ssp. inyoensis* - Inyo mule deer O. hemionus ssp. cedrosensis or cerrosensis* - Cedros Island mule deer For the purpose of this write-up, life history, basic requirements, and management for mule deer and black-tailed deer will be combined, unless an aspect differs significantly. ORDER : Artiodactyla CLASS : Mammal FEDERAL LEGAL STATUS : No special status OTHER STATUS : The Cedros Island mule-deer, ssp. cedrocensis, is endangered [46]. COMPILED BY AND DATE : S. A. Snyder, June 1991 LAST REVISED BY AND DATE : NO-ENTRY AUTHORSHIP AND CITATION : Snyder, S. A. 1991. Odocoileus hemionus. In: Remainder of Citation

WILDLIFE DISTRIBUTION AND OCCURRENCE

WILDLIFE SPECIES: Odocoileus hemionus | Mule Deer
GENERAL DISTRIBUTION : Mule deer inhabit western North America from northern British Columbia and Alberta south through central Mexico. Black-tailed deer occur from southern, coastal Alaska south along the coast through northern California. Ranges for each subspecies are listed below [9,18,35,52,54]: ssp. hemionus - central Arizona and New Mexico north to northern British Columbia, Alberta, and central Saskatchewan; west-central British Columbia, Washington, Oregon, and east through central North and South Dakota, Nebraska, and Kansas; northeast corner of California and scattered sightings in Missouri, Minnesota, and Iowa ssp. crooki - possibly the Texas Panhandle; southern Arizona and New Mexico; southwestern Texas and into Mexico ssp. californicus - south coastal and east-central California ssp. fuliginatus - northern Baja California into southern California ssp. peninsulae - southern Baja California ssp. columbianus - coastal British Columbia, including Vancouver Island, south through coastal Washington, Oregon, and through California into Santa Barbara County ssp. sitkensis - Alexander Archipelago, Alaska into western British Columbia and the southern fringe of Yukon Territory; areas in Alaska include Prince William Sound and its islands; Kodiak, Afognak, Prince of Wales, and Queen Charlotte Islands, and the Yakutat area. ssp. eremicus - possibly an isolated portion of southeastern California along the Colorado River ssp. sheldoni - possibly Tiburon Island, Baja California, Mexico ssp. inyoensis - possibly the eastern slope of the southern Sierra Nevada, California ssp. cedrosensis - Cedros Island, Baja California ECOSYSTEMS : FRES20 Douglas-fir FRES21 Ponderosa pine FRES22 Western white pine FRES23 Fir-spruce FRES24 Hemlock-Sitka spruce FRES25 Larch FRES26 Lodgepole pine FRES27 Redwood FRES28 Western hardwoods FRES29 Sagebrush FRES30 Desert shrub FRES31 Shinnery FRES32 Texas savanna FRES33 Southwestern shrubsteppe FRES34 Chaparral-mountain shrub FRES35 Pinyon-juniper FRES36 Mountain grasslands FRES37 Mountain meadows FRES38 Plains grasslands FRES39 Prairie FRES40 Desert grasslands FRES41 Wet grasslands FRES42 Annual grasslands FRES44 Alpine STATES :
AK AZ AR CA CO ID IA KS MN MO MT
NE NV NM ND OK OR SD TX UT WA WY

AB BC MB SK YK

MEXICO
BLM PHYSIOGRAPHIC REGIONS : 1 Northern Pacific Border 2 Cascade Mountains 3 Southern Pacific Border 4 Sierra Mountains 5 Columbia Plateau 6 Upper Basin and Range 7 Lower Basin and Range 8 Northern Rocky Mountains 9 Middle Rocky Mountains 10 Wyoming Basin 11 Southern Rocky Mountains 12 Colorado Plateau 13 Rocky Mountain Piedmont 14 Great Plains 15 Black Hills Uplift 16 Upper Missouri Basin and Broken Lands KUCHLER PLANT ASSOCIATIONS : K001 Spruce - cedar - hemlock forest K002 Cedar - hemlock - Douglas-fir forest K003 Silver fir - Douglas-fir forest K004 Fir - hemlock forest K005 Mixed conifer forest K006 Redwood forest K007 Red fir forest K008 Lodgepole pine - subalpine forest K009 Pine - cypress forest K010 Ponderosa shrub forest K011 Western ponderosa forest K012 Douglas-fir forest K013 Cedar - hemlock - pine forest K014 Grand fir - Douglas-fir forest K015 Western spruce - fir forest K017 Black Hills pine forest K018 Pine - Douglas-fir forest K019 Arizona pine forest K020 Spruce - fir - Douglas-fir forest K021 Southwestern spruce - fir forest K022 Great Basin pine forest K023 Juniper - pinyon woodland K024 Juniper steppe woodland K025 Alder - ash forest K026 Oregon oakwoods K027 Mesquite bosque K028 Mosaic of K002 and K026 K029 California mixed evergreen forest K030 California oakwoods K031 Oak - juniper woodland K032 Transition between K031 and K037 K033 Chaparral K034 Montane chaparral K035 Coastal sagebrush K036 Mosaic of K030 and K035 K037 Mountain-mahogany - oak scrub K038 Great Basin sagebrush K039 Blackbrush K040 Saltbush - greasewood K041 Creosotebush K042 Creosotebush - bursage K043 Paloverde - cactus shrub K044 Creosotebush - tarbush K045 Ceniza shrub K047 Fescue - oatgrass K048 California steppe K049 Tule marshes K050 Fescue - wheatgrass K051 Wheatgrass - bluegrass K052 Alpine meadows and barren K053 Grama - galleta steppe K054 Grama - tobosa prairie K055 Sagebrush steppe K056 Wheatgrass - needlegrass shrubsteppe K057 Galleta - threeawn shrubsteppe K058 Grama - tobosa shrubsteppe K059 Trans-Pecos shrub savanna K060 Mesquite savanna K061 Mesquite - acacia savanna K062 Mesquite - live oak savanna K063 Foothills prairie K064 Grama - needlegrass - wheatgrass K065 Grama - buffalograss K066 Wheatgrass - needlegrass K067 Wheatgrass - bluestem - needlegrass K068 Wheatgrass - grama - buffalograss K069 Bluestem - grama prairie K070 Sandsage - bluestem prairie K071 Shinnery K076 Blackland prairie K085 Mesquite - buffalograss K086 Juniper - oak savanna K087 Mesquite - oak savanna K088 Fayette prairie K098 Northern floodplain forest SAF COVER TYPES : 16 Aspen 18 Paper birch 42 Bur oak 66 Ashe juniper - redberry (Pinchot) juniper 67 Mohrs ("shin") oak 68 Mesquite 201 White spruce 202 White spruce - paper birch 203 Balsam poplar 204 Black spruce 205 Mountain hemlock 206 Engelmann spruce - subalpine fir 207 Red fir 208 Whitebark pine 209 Bristlecone pine 210 Interior Douglas-fir 211 White fir 212 Western larch 213 Grand fir 215 Western white pine 216 Blue spruce 217 Aspen 218 Lodgepole pine 219 Limber pine 220 Rocky Mountain juniper 221 Red alder 222 Black cottonwood - willow 223 Sitka spruce 224 Western hemlock 225 Western hemlock - Sitka spruce 226 Coastal true fir - hemlock 227 Western redcedar - western hemlock 228 Western redcedar 229 Pacific Douglas-fir 230 Douglas-fir - western hemlock 231 Port-Orford-cedar 232 Redwood 233 Oregon white oak 234 Douglas-fir - tanoak - Pacific madrone 235 Cottonwood - willow 236 Bur oak 237 Interior ponderosa pine 238 Western juniper 239 Pinyon - juniper 240 Arizona cypress 241 Western live oak 242 Mesquite 243 Sierra Nevada mixed conifer 244 Pacific ponderosa pine - Douglas-fir 245 Pacific ponderosa pine 246 California black oak 247 Jeffrey pine 248 Knobcone pine 249 Canyon live oak 250 Blue oak - Digger pine 251 White spruce - aspen 252 Paper birch 253 Black spruce - white spruce 254 Black spruce - paper birch 255 California coast live oak 256 California mixed subalpine SRM (RANGELAND) COVER TYPES : NO-ENTRY PLANT COMMUNITIES : Mule deer and black-tailed deer together inhabit virtually every major vegetative type in western North America except those in the tropics, arctic, and extreme deserts [35,54]. Generally black-tailed deer inhabit the temperate, coniferous forests along the northern Pacific Coast, from northern California to Alaska. They inhabit spruce (Picea spp.)-fir (Abies spp.)-hemlock (Tsuga spp.) forests as well as pine (Pinus spp.)-Douglas-fir (Pseudotsuga menziesii) and lodgepole pine (Pinus contorta)-subalpine fir (Abies lasiocarpa) forests. Some black-tailed deer also occur in the chaparral communities south of the central Coast Ranges of California. Mule deer inhabit grass-dominated plains and prairies, shrublands, woodlands, and mountain forests from south coastal Alaska south through Canada and the United States, and into Mexico. They are found in the semideserts of the Southwest and Great Basin region, as well as the high mountains of the Northwest [35,52,54]. REFERENCES : NO-ENTRY

BIOLOGICAL DATA AND HABITAT REQUIREMENTS

WILDLIFE SPECIES: Odocoileus hemionus | Mule Deer
TIMING OF MAJOR LIFE HISTORY EVENTS : Mating Season - usually begins in November and continues through December in the north; may begin in December and continue through January in warmer climates; can begin in September for black-tailed deer Gestation - about 6 or 7 months Birthing Season - usually begins in June and can continue into August; may begin in April for black-tailed deer; mature females commonly have twins, while yearlings have only single fawns Age of Maturity - about 1 1/2 years for females; young males may not mate due to competition with older males Lifespan - females as long as 22 years; males as long as 16 years; 8 to 10 years is considered old for both Antlers - males only; begin shedding in December and continues into March; mature and less healthy males may shed earlier [35] PREFERRED HABITAT : Mule deer are most likely to be found in open forested regions or on the plains and prairies. They prefer rocky or broken terrain at elevations near or at the subalpine zone in the mountainous regions of the West [8]. They are also found in alpine, montane, and foothill zones. Mule deer seek shelter at lower elevations when snows become deep. In the mountains of the Southwest, mule deer are found in lower elevation shrublands, while white-tailed deer occupy the higher elevation montane areas. In open prairie regions mule deer tend to concentrate in river breaks and brushy streambottoms [35]. In the high ranges of the Rocky Mountains, mule deer migrate during winter, sometimes moving 50 to 100 miles (80-160 km) [35,54]. COVER REQUIREMENTS : Mule deer are better adapted to open areas than white-tailed deer, although cover becomes important in winter. Areas where cover can prevent snow from accumulating beyond 12 inches (30 cm) are most beneficial [18,39]. Wallmo and Schoen [53] reported that mule deer can cope with snow up to 24 inches (60 cm) if not dense or crusty. In Alaska during winter black-tailed deer use old-growth forests at low elevations, where forage becomes abundant after the stand exceeds 300 years in age and canopy cover is 60 to 80 percent [18]. During snow-free periods, black-tailed deer move to less dense stands and subalpine meadows [42]. In the Cariboo Region of British Columbia winter range is defined as those areas with 10 to 45 percent slope, having a south and/or west aspect, and below 4,950 feet (1,500 m) in shallow to moderate snowpack zones, or below 3,300 feet (1,000 m) in deep snowpack zones [1]. Lackenby and others [33] and Black and others [5] listed optimal cover attributes for the Great Basin shrubsteppe region, including estimates of tree heights and canopy closure for thermal, hiding, fawning, and foraging cover. They estimated the proportion of cover to forage at 55 percent forage, 20 percent hiding cover, 10 percent thermal cover, 10 percent fawn-rearing cover, and 5 percent fawn habitat. FOOD HABITS : Mule deer are primarily browsers, feeding on several thousand different plant species across their range. They are capable of altering or severely damaging plant communities through overbrowsing [40]. Mule deer consume leaves, stems, and shoots of woody plants most often during summer and fall, while grasses and forbs compose the bulk of spring diets. However, feeding behavior is quite variable in any given location. Some of the most common foods are: rabbitbrush (Chrysothamnus spp.), mountain-mahogany (Cercocarpus spp.), snowberry (Symphoricarpos spp.), buffaloberry (Shepherdia spp.), ceanothus (Ceanothus spp.), rose (Rosa spp.), serviceberry (Amelanchier spp.), sagebrush (Artemisia spp.), sumac (Rhus spp.), common chokecherry (Prunus virginiana), willow (Salix spp.), Gambel oak (Quercus gambellii), mockorange (Philadelphus lewisii), ninebark (Physocarpus spp.), antelope bitterbrush (Purshia tridentata), mariposa (Calochortus elegans), juniper (Juniperus spp.), yucca (Yucca spp.), eurphorbia (Euphorbia spp.), manzanita (Arctostaphylos spp.), lechuguilla (Agave lechuguilla), western yarrow (Achillea millefolium), red huckleberry (Vaccinium parvifolium), swordfern (Polystichum munitum), milkvetch (Astragalus spp.), and dandelion (Taraxacum officinale). Grasses include bluegrasses (Poa spp.), wheatgrasses (Agropyron spp.), and bromes (Bromus spp.) [17,18,19,21,25,30,35,36,42,48,49,56]. PREDATORS : Mule deer predators include humans, domestic dogs (Canis familiaris), coyotes (Canis latrans), wolves (Canis lupus), black bears (Ursus americanus), grizzly bears (U. arctos), mountain lions (Felis concolor), lynx (F. lynx), bobcats (F. rufus), and golden eagles (Aquilla chrysaetos) [35]. MANAGEMENT CONSIDERATIONS : The effects of logging on mule deer populations vary between and within regions; therefore it is difficult to generalize conclusions [34]. Site-specific studies are required to determine logging effects, although many studies confirm that slash depth is a major factor limiting mule deer use of harvested areas [1,18,27,34,53]. Studies in Alaska have shown that black-tailed deer avoid second-growth forests after 20 to 30 years, and instead turn to "over-mature" forests (older than 300 years) because these forests provide more browse than younger stands [18,27,53]. Happe and others [19] have shown that forage in coastal old-growth forests has higher crude protein values than forage in clearcuts. Tannin astringency of browse, which reduces digestive protein, is higher in clearcuts than in old-growth forests. Hanley [18] recommended scattering clearcuts in old-growth in irregular shapes and spreading them over a wide elevational range. A study in Colorado showed that mule deer increased after 10 years following a treatment of alternating clearcuts with uncut strips in lodgepole pine-spruce-fir forests. Strips 100 feet (30 m) wide produced the best results [51]. Wallmo and Schoen [53] listed management guidelines for timber harvesting that benefit deer in the western United States. However, they stated that some of these guidelines are based on speculation and all contradict claims that large clearcuts are better for mule deer. Mule deer are vulnerable to a variety of viral, fungal, and bacterial diseases [20]. They inflict heavy crop damage and damage to hayfields, stackyards, and orchards, as well as reforestation projects. Mule deer are often attacked and killed by domestic dogs, and several hundred thousand deer are killed by vehicles each year [40]. Mule deer are not as tolerant of human activity and not as adaptable to disturbances as white-tailed deer [40]. REFERENCES : NO-ENTRY

FIRE EFFECTS AND USE

WILDLIFE SPECIES: Odocoileus hemionus | Mule Deer
DIRECT FIRE EFFECTS ON ANIMALS : Although uncommon, mule deer can be trapped and killed by fast-moving fires [9,21]. HABITAT RELATED FIRE EFFECTS : The effects of fire on mule deer habitat are widely varied and well documented in the literature. In general, fires that create mosaics of forage and cover are beneficial. Deer seem to prefer foraging in burned compared to unburned areas, although preference may vary seasonally [4,12,13,23,24,25,28,58]. This preference may indicate an increase in plant nutrients which usually occurs following fire [2,22,43]. Hobbs and Spowart [22] warned about making conclusions regarding the benefits of fire based on forage studies alone. Their study of fire on nutrition in Colorado revealed increases in the quality of deer diets due to changes in forage selection--not increases in nutrients of previously selected forage. Burning in grassland communities reduces litter that otherwise inhibits new growth of grasses. Fire rejuvenates and improves these grasslands, which are important winter range in some areas [23,58]. Burning sagebrush communities can result in significant increases of herbaceous plants by reducing decadent sagebrush that outcompetes more nutritious and palatable species [44,47]. However, in areas where sagebrush is the only cover, its complete removal can be detrimental to mule deer populations [47]. Antelope bitterbrush is a highly preferred browse species on some mule deer winter ranges and is sensitive to burning [17,50]. Burned bitterbrush takes longer to recover than bitterbrush disturbed by other means [50]. Burned bitterbrush grows slower, is less dense, and plants are smaller than unburned specimens. Bitterbrush responds variably to fire intensity, temperature, and season [17]. Late summer fires in Idaho killed two-thirds of the bitterbrush, while a moderate-intensity spring fire in Montana killed one-third. A summer fire of moderate intensity in Oregon destroyed the entire stand of bitterbrush [17]. Shrubs and forbs in pinyon (Pinus spp.)-juniper (Juniperus spp.) communities tend to increase the first few years following fire, providing valuable browse [6,37]. Mule deer seem to use these areas more after 15 years [37,45]. Stager and Klebenow [45] reported that the beneficial effects of fire for mule deer in pinyon-juniper stands can last as long as 115 years. However, Bunting [7] concluded that burning of these stands becomes increasingly difficult as stands grow older because fine fuels in the understory are reduced. He stated that burning should take place at early successional stages and at intervals based on the fire tolerance of desirable forage species. Everett [14] warned that preburn conditions in pinyon-juniper stands will most likely determine the postfire plant composition. If perennial shrubs are present before a burn, they will come back following fire. If no shrubs are present, perennial grasses will develop [6]. FIRE USE : Fire can be used to stimulate browse, create openings in dense, inaccessible plant communities, and reduce slash, as well as increase nutrient content and palatability of forage [11,17,38]. Gruell [17] listed several factors that influence postfire plant composition, including the severity, size, and season of the burn, fuel type, postburn foraging intensity, and the preburn plant community composition. He stated that surface fires of moderate intensity following thinning or selection cuts can improve Douglas-fir or ponderosa pine (Pinus ponderosa) forests for mule deer by promoting regeneration of crown-sprouting shrubs and preparing the seedbed for herbs and shrubs. A mosaic of seral stages is best for mule deer [17]. In areas where chaparral adjoins oak woodlands, prescribed burns can create access through the chaparral to the understory forage of the oak woodlands [28]. Biswell [4] recommended burning chaparral every 30 years to create a mosaic of young stands. Late summer or early fall burning promotes the highest seed crop for most species in these plant communities. Wallmo and others [55] listed several recommendations for burning chaparral communities to improve mule deer habitat. Fire can control pinyon-juniper woodlands by maintaining them in a subclimax state [6]. Small burns are more beneficial than large burns to mule deer because they tend to use burned areas close to cover. The optimum width for burns in these communities may be less than 0.25 mile (0.4 km) [6]. To maintain forage in bunchgrass communities, burning at 4- to 6-year intervals in winter or early spring is recommended [23]. Burning can control sagebrush in areas where it has dominated grasslands and reduced deer forage [47]. Where Gambel oak grows thick and impenetrable, fire can open stands and provide valuable winter range for mule deer [32]. Kufeld [31] recommended burning Gambel oak in autumn during or immediately following leaf fall and building fire breaks 26 feet wide (8 m) around the areas to be burned. Because Gambel oak recovers quickly following fire, particularly at low elevations where mule deer winter, its growth must be monitored and retarded to improve mule deer habitat [32]. REFERENCES : NO-ENTRY

References for species: Odocoileus hemionus


1. Permar, T. A.; Fisher, R. F. 1983. Nitrogen fixation and accretion by wax myrtle (Myrica cerifera) in slash pine (Pinus elliottii) plantations. Forest Ecology and Management. 5: 39-46. [15006]
2. Asherin, Duane A. 1973. Prescribed burning effects on nutrition, production and big game use of key northern Idaho browse species. Moscow, ID: University of Idaho. 96 p. Dissertation. [360]
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. Biswell, Harold H. 1989. Prescribed burning in California wildlands vegetation management. Los Angeles, CA: University of California Press. 255 p. [13700]
5. Black, Hugh; Scherzinger, Richard J.; Thomas, Jack Ward. 1976. Relationships of Rocky Mountain elk and Rocky Mountain mule deer habitat to timber management in the Blue Mountains of Oregon and Washington. In: Hieb, S. R.,, ed. Elk-logging-roads: Proceedings of the symposium; 1975 December 16-17; Moscow, ID. Moscow, ID: University of Idaho: 11-31. [14367]
6. Blackburn, W. H.; Beall, R.; Bruner, A.; [and others]. 1975. Controlled fire as a management tool in the pinyon-juniper woodland, Nevada. Annual Progress Report FY 1975. Unpublished report on file with: U.S. Department of Agriculture, Forest Service, Intermountain Research Station, Fire Sciences Laboratory, Missoula, MT. 77 p. [453]
7. Bunting, Stephen C. 1987. Use of prescribed burning in juniper and pinyon-juniper woodlands. In: Everett, Richard L., compiler. Proceedings--pinyon-juniper conference; 1986 January 13-16; Reno, NV. Gen. Tech. Rep. INT-215. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Research Station: 141-144. [4836]
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12. Davis, Peter R. 1976. Response of vertebrate fauna forest fire and clearcutting in south central Wyoming. Final Report Cooperative Agreements Nos. 16-391-CA and 16-464-CA, U.S. Department of Agriculture, Forest Service and University of Wyoming. Laramie, WY: University of Wyoming, Department of Zoology and Physiology. 94 p. [318]
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21. Hines, William W. 1973. Black-tailed deer populations and Douglas-fir reforestation in the Tillamook Burn, Oregon. Game Research Report Number 3. Federal Aid to Wildlife Restoration, Project W-51-R, Final Report. Corvallis, OR: Oregon State Game Commission. 59 p. [8431]
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25. Keay, Jeffrey A.; Peek, James M. 1980. Relationships between fires and winter habitat of deer in Idaho. Journal of Wildlife Management. 44(2): 372-380. [125]
26. Kie, John G. 1984. Deer habitat use after prescribed burning in northern California. Res. Note PSW-369. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station. 3 p. [14393]
27. Kirchhoff, Matthew D. 1983. Black-tailed deer use in relation to forest clearcut edges in southeastern Alaska. Journal of Wildlife Management. 47(2): 497-501. [14395]
28. Klinger, Robert C.; Kutilek, Michael J.; Shellhammer, Howard S. 1989. Population responses of black-tailed deer to prescribed burning. Journal of Wildlife Management. 53(4): 863-871. [10686]
29. 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]
30. Kufeld, Roland C.; Wallmo, O. C.; Feddema, Charles. 1973. Foods of the Rocky Mountain mule deer. Res. Pap. RM-111. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Forest and Range Experiment Station. 31 p. [1387]
31. Kufeld, Roland C. 1983. Responses of elk, mule deer, cattle, and vegetation to burning, spraying and chaining of Gambel oak rangeland. Tech. Publ. 34. Fort Collins, CO: Colorado Division of Wildlife. 47 p. [253]
32. Kunzler, L. M.; Harper, K. T. 1980. Recovery of Gambel oak after fire in central Utah. The Great Basin Naturalist. 40(2): 127-130. [1389]
33. Leckenby, Donavin A.; Sheehy, Dennis P.; Nellis, Carl H.; [and others]. 1982. Wildlife habitats in managed rangelands--the Great Basin of southeastern Oregon: mule deer. Gen. Tech. Rep. PNW-139. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station. 40 p. [1432]
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36. Maser, Chris; Mate, Bruce R.; Franklin, Jerry F.; Dyrness, C. T. 1981. Natural history of Oregon Coast mammals. Gen. Tech. Rep. PNW-133. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station. 496 p. [10238]
37. McCulloch, Clay Y. 1969. Some effects of wildfire on deer habitat in pinyon-juniper woodland. Journal of Wildlife Management. 33(4): 778-784. [1594]
38. Nelson, Jack R. 1976. Forest fire and big game in the Pacific Northwest. In: Proceedings, annual Tall Timbers fire ecology fire ecolgy conference: Pacific Northwest; 1974 October 16-17; Portland, OR. No. 15. Tallahassee, FL: Tall Timbers Research Station: 85-102. [6464]
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