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Introductory

WILDLIFE SPECIES: Alces alces | Moose
ABBREVIATION : ALAL COMMON NAMES : moose European elk Shiras moose Alaskan moose TAXONOMY : There are seven subspecies of moose worldwide, four of which are found in North America. They are differentiated by size, color, palate shape, and geographic distribution [34]. Alces alces ssp. gigas A. alces ssp. shirasi A. alces ssp. andersoni A. alces ssp. americana ORDER : Artiodactyla CLASS : Mammal FEDERAL LEGAL STATUS : No special status OTHER STATUS : Moose numbers fluctuate periodically in any given location, sometimes reaching critically low numbers and other times abundant. Populations are influenced by weather, predators, food availability, and human disturbance, particularly hunting pressure [6,14]. COMPILED BY AND DATE : S. A. Snyder, May 1991 LAST REVISED BY AND DATE : NO-ENTRY AUTHORSHIP AND CITATION : Snyder, S. A. 1991. Alces alces. In: Remainder of Citation

WILDLIFE DISTRIBUTION AND OCCURRENCE

WILDLIFE SPECIES: Alces alces | Moose
GENERAL DISTRIBUTION : The moose can be found throughout Scandanavia, northern Asia, and northern North America. In North America, the subspecies gigas ranges from northwestern British Columbia into western Yukon Territory and throughout most of Alaska. Subspecies shirasi can be found in western Wyoming, north and central Idaho, western Montana, southwestern Alberta, southeastern British Columbia, and in isolated areas of Utah, Colorado, and extreme northwestern Washington. Subspecies andersoni ranges from northern Minnesota, Wisconsin, and Michigan into western Ontario, west to central British Columbia, and north to eastern Yukon Territory and the Northwest Territories. Subspecies americana ranges from Maine and Nova Scotia, west through Quebec and central Ontario, and from Hudson Bay south to the Great Lakes [34]. ECOSYSTEMS : FRES10 White-red-jack pine FRES11 Spruce-fir FRES19 Aspen-birch FRES20 Douglas-fir FRES21 Ponderosa pine FRES22 Western white pine FRES23 Fir-spruce FRES25 Larch FRES26 Lodgepole pine FRES28 Western hardwoods FRES37 Mountain meadows STATES :
AK CO ID ME MI MN MT
NH UT WA WI WY

AB BC MB NB NF NT NS ON
PE PQ SK YT
BLM PHYSIOGRAPHIC REGIONS : 5 Columbia Plateau 8 Northern Rocky Mountains 9 Middle Rocky Mountains 10 Wyoming Basin 11 Southern Rocky Mountains KUCHLER PLANT ASSOCIATIONS : K001 Spruce - cedar - hemlock forest K002 Cedar - hemlock - Douglas-fir forest K004 Fir - hemlock forest K005 Mixed conifer forest K008 Lodgepole pine - subalpine forest K012 Douglas-fir forest K013 Cedar - hemlock - pine forest K014 Grand fir - Douglas-fir forest K015 Western spruce - fir forest K020 Spruce - fir - Douglas-fir forest K093 Great Lakes spruce - fir forest K094 Conifer bog K095 Great Lakes pine forest K096 Northeastern spruce - fir forest SAF COVER TYPES : 1 Jack pine 5 Balsam fir 12 Black spruce 13 Black spruce - tamarack 15 Red pine 16 Aspen 17 Pin cherry 18 Paper birch 21 Eastern white pine 22 White pine - hemlock 23 Eastern hemlock 24 Hemlock - yellow birch 30 Red spruce - yellow birch 32 Red spruce 33 Red spruce - balsam fir 35 Paper birch - red spruce - balsam fir 37 Northern white cedar 38 Tamarack 107 White spruce 201 White spruce 202 White spruce - paper birch 203 Balsam poplar 204 Black spruce 205 Mountain hemlock 206 Engelmann spruce - subalpine fir 208 Whitebark pine 210 Interior Douglas-fir 212 Western larch 213 Grand fir 215 Western white pine 216 Blue spruce 217 Aspen 218 Lodgepole pine 219 Limber pine 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 235 Cottonwood - willow 251 White spruce - aspen 252 Paper birch 254 Black spruce - paper birch SRM (RANGELAND) COVER TYPES : NO-ENTRY PLANT COMMUNITIES : Moose are found throughout the boreal forests of North America. They inhabit jack pine (Pinus banksiana)-balsam fir (Abies balsamea) forests mixed with paper birch (Betula papyrifera) and quaking aspen (Populus tremuloides). They also inhabit white spruce (Picea glauca)-black spruce (P. mariana) forests mixed with birch (Betula spp.) and willow (Salix spp.) [12,39]. In the West moose inhabit Douglas-fir (Pseudotsuga menziesii)/ninebark (Physocarpus malvaceous) habitat types, with snowberry (Symphoricarpus albus), redosier dogwood (Cornus sericea) and willow. Moose are also found in grand fir (Abies grandis)-Pacific yew (Taxus brevifolia) forests and subalpine fir (Abies lasiocarpa)- Engelmann spruce (Picea engelmannii) types with aspen [22,36,37]. Moose use riparian communities and herbacious bogs. Moose are capable of altering the species composition of plant communities and the overall character of communities through overbrowsing [8,17]. REFERENCES : NO-ENTRY

BIOLOGICAL DATA AND HABITAT REQUIREMENTS

WILDLIFE SPECIES: Alces alces | Moose
TIMING OF MAJOR LIFE HISTORY EVENTS : Mating - September through October Gestation - 8 months Calving Season - May through June; occasional twinning occurs if females receive more than adequate nutrition Lifespan - 20 or more years; average 16 years Age of Maturity - capable of reproducing at 16 months; however, females usually produce first calf at 2 to 3 years; moose reach full maturity at 5 or 6 years, with maximum fecundity of 10 to 11 years Antlers - only males have antlers, which are shed between November and January Home Range - varies from 116 square miles (300 sq km) in Alaska to 8 to 15 square miles (20-40 sq km) in northeastern North America [6,34,43]. PREFERRED HABITAT : Moose habitat preferences vary with the season. In summer moose can be found in open plant communities where forage is abundant, such as riparian communities and cutover stands older than 15 years. Moose seem to use bogs and other aquatic areas more frequently in summer and in disproportion to their availability [5]. During winter moose prefer forested areas and move into denser, conifer-dominated forests as the winter progresses. In mountainous areas of the West, moose concentrate at elevations below 3,500 feet (1,067 m) during winter. During summer they move to higher elevations, usually above 5,000 feet (1,524 m) [11,29,37]. Moose distribution in winter is limited by the availability of woody food plants and by snow conditions, such as depth, density, hardness, and duration [14,46]. COVER REQUIREMENTS : Moose need a variety of habitats from dense coniferous forests to more open aquatic and riparian communities with some cover. Moose seek dense forests during mid to late winter as snows deepen and harden. Cover becomes more essential than forage during winter [24,33,35,38]. Pierce and Peek [37] noted that, in winter, moose in the Clearwater Drainage of Idaho use dense stands characterized by broken canopies and dominated by subalpine fir (Abies lasiocarpa) and grand fir, with Pacific yew as the dominant understory and preferred forage. Allen and others [1] reported the quality of winter cover increases as the proportion of conifers increases. Ideal winter range is composed of conifers taller than 18 feet (6 m), with a canopy closure of 75 percent or greater. Cover becomes critical during severe winters in areas where snow depth exceeds 40 inches (100 cm) because at these depths moose are impeded [1,43,46]. For calving, cows need dense cover bordering younger stands which provide substantial food. Cow/calf movements are restricted because calves cannot wade through deep snow. FOOD HABITS : Moose are generalist, ruminant herbivores. Their foods encompass several hundred species worldwide, but moose usually eat about 25 to 30 species in any one locale [43]. Thoughout their range in North America, moose most commonly browse on alder (Alnus spp.), cottonwood (Populus spp.), willow, birch, aspen, and balsam fir. Following is a list of other species frequently found in moose diets: serviceberry (Amelanchier spp.), mountain ash (Sorbus spp.), bush honeysuckle (Diervilla lonicera), dogwood, mountain maple (Acer spicatum), Rocky Mountain maple (Acer glabrum), viburnum (Viburnum spp.), current (Ribes spp.), ceanothus (Ceanothus spp.), huckleberry (Vaccinium spp.), cherry (Prunus spp.), Pacific yew, and wild sarsaparilla (Aralia nudicaulis). Moose also eat various species of mushrooms, sedges (Carex spp.), grasses, such as bluegrass (Poa spp.) and brome (Bromus spp.), lichens (Peltigera spp.), and forbs, such as fireweed (Epilobium spp.) and lupine (Lupinus spp.) [1,13,16,28,34,36,38,40]. Some preferred aquatic species include water horsetail (Equisetum fluviatile), burreed (Sparganium spp.), and pondweed (Potomageton spp.) [47]. In Newfoundland Dodds [15] noted competition between snowshoe hares (Leupus americanus) and moose for browse. PREDATORS : Moose predators include humans, wolves (Canis lupus), grizzly bears (Ursus arctos), and black bears (U. americanus) [27,34]. MANAGEMENT CONSIDERATIONS : In the past wildlife managers have assumed that clearcuts were beneficial to moose because such cuts favor abundant browse production. In general this is true; however, moose require at least some cover during every season and usually will not venture into large, open areas with no hiding cover. Stelfox and others [41] reported that moose used clearcuts after 17 years only if adequate shelter was available in interspersed stands nearby. Matchett [29] reported that moose select cutover areas that are more vegetated than not; these are usually at least 10 to 30 years old. He concluded that for the Yaak River Drainage in western Montana, cutting units should be less than 49 acres (20 ha), and cutting units over large areas should exhibit a diversity of silvicultural methods. Three hundred and twenty feet (100 m) of timber should be left between cutting units, and road closures should be imposed. Costain [11] recommended maintaining timber in stream bottoms with a minimum of 300 feet (91 m) between cutting units. In most cases moose will not use clearcuts until adequate cover has been established, usually in 15 years. Moose select for edges along islands of residual timber within cuts, as opposed to edges of large cuts [30]. Pierce and Peek [37] recommended maintaining grand fir old-growth with a yew understory because of the importance of this type to wintering moose. In western Canada hundreds of moose are killed each year by trains. This factor may be holding moose populations below their potential [10]. REFERENCES : NO-ENTRY

FIRE EFFECTS AND USE

WILDLIFE SPECIES: Alces alces | Moose
DIRECT FIRE EFFECTS ON ANIMALS : Occasionally moose are trapped and killed by fire [20]. HABITAT RELATED FIRE EFFECTS : An extensive review of the literature indicates that fire generally enhances moose habitat by creating and maintaining seral communities, and is considered beneficial to moose populations [14,49,50]. The beneficial effects of fire on habitat were estimated to last less than 50 years, with moose density peaking 20 to 25 years following fire [50]. Much research has been conducted on fire-moose relationships in Alaska. Bishop and Rausch [5] stated that fire-created seral communities have been the major influence on increasing moose numbers. A study conducted by Gasaway and DuBois [20] showed that moose were not displaced from their summer home range when a portion of it was burned. Moose used unburned vegetation both within and outside the burned area. The fire burned in spring, allowing vegetation to resprout for use during the summer. However, extremely large, hot, and fast-moving wildfires can force moose to temporarily abandon their home ranges. MacCracken and Viereck [49] reported that following a spring fire browse for moose was abundant within 2 months. Aspen, birch, and willow sprouted from roots and stumps, and this response was closely related to the prefire stand age. Young (70-year-old) aspen-white spruce-black spruce stands produce 10 times more forage than older stands (130 to 180-year-old). Krefting [46] discussed the importance of fire to the Isle Royale moose population. He stated that fire is the primary agent responsible for maintaining the secondary successional vegetation that moose prefer. Hansen and others [48] reported that the moose population of Isle Royale quadrupled in the decade following a 1936 fire that burned 26,000 acres (10,526 ha). At this time there were no predators on the island. Wolf and Zasada [45] reported that aspen provided the most browse 1 to 5 years after fire, while birch and willow provided the most browse 10 to 16 years after fire. Others reported similar findings and noted a decrease in browse production after 20 years [31,44,45]. However, fires do not always stimulate aspen-birch-willow communities [9]. Following fire in the boreal forest there is usually a period of 5 to 20 years and occasionally 60 to 70 years when moose foraging conditions are favorable. Duration of browse growth and volume produced is variable, however. In Alaska a single, well-timed reburn could increase browse by reducing white spruce [40]. Five years after a 40-acre (16 ha) fire in the Gallatin National Forest, Montana, aspen increased from a few hundred stems per acre to over 30,000 stems per acre (74,100/ha). Shrubs sprouted vigorously from rootstocks, with willow producing a greater canopy and crown volume than prefire conditions allowed [22]. Frequent fires can destroy most of the humus layer and reduce the regeneration of quaking aspen. Fires at 2- to 3-year intervals during the regeneration stage may entirely destroy the suckering capability of aspen. In older aspen stands fire seldom harms root systems enough to destroy suckering [7]. A study in Idaho showed that burning Rocky Mountain maple increased the crude fiber content, resulting in decreased digestibility. Moisture and crude protein in willow and serviceberry (Amelanchier alnifolia) increased significantly during postfire year 1 but began to decrease by postfire years 2 and 3 [2]. Bangs and Bailey [3] stated that hot fires in hot weather probably would not produce much beneficial edge habitat. They also concluded that calf recruitment could be low in springs following fires that reduce vegetation on wintering grounds. FIRE USE : In willow-birch-aspen forest types, burning every 15 to 20 years will increase forage production for moose and maintain a vegetation height of about 9 feet (3 m), which is within foraging reach of moose [31]. Spring or early summer burning allows for some forage regrowth in the same year. Late summer or fall burning in northern latitudes will delay forage regrowth until the following spring, reducing winter food [20,49]. Areas where forage species are killed by fire must be seeded, which delays browse production by 3 to 5 years [45]. Fires can be used to intersperse new and old growth cover, and increase the edge effect. To create a mosaic of stand age classes, burning should be discontinuous. This allows moose to remain in immediate areas during a burn. Also a variety of plant communities should be burned to provide immediate and long-term browse, as well as a diversity of forage species [49]. Dense coniferous forests must always be maintained adjacent to more open areas with high forage production. Openings should be no larger than 40 to 50 acres (16-20 ha) in areas of dense cover and less in more open habitats [14,22]. Pierce and Peek [37] concluded that piling and burning is better than broadcast burning in selection-cut grand fir-yew stands in order to maintain the essential yew browse understory. However, caution must be taken when burning these areas because of Pacific yew's sensitivity to fire. Fire can be used to maintain aspen communities and keep out balsam fir and white spruce where these types succeed aspen [46]. REFERENCES : NO-ENTRY

REFERENCES

WILDLIFE SPECIES: Alces alces | Moose
REFERENCES : 1. Allen, Arthur W.; Jordan, Peter A.; Terrell, James W. 1987. Habitat suitability index models: moose, Lake Superior region. Biol. Rep. 82 (10.155). Washington, DC: U.S. Department of the Interior, Fish and Wildlife Service. 47 p. [11710] 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. Bangs, Edward E.; Bailey, Theodore N. 1983. Interrelationships of weather, fire, and moose on the Kenai National Moose Range, Alaska. In: Proceedings, North American moose conference workshop. 16: 255-274. [10735] 4. 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] 5. Bishop, R. H.; Rausch, R. A. 1974. Moose population fluctuations in Alaska, 1950-1972. Le Naturaliste Canadien. 101: 559-593. [13117] 6. Bishop, Richard H. 1988. The moose in Alaska. In: Chandler, William J.; Labate, Lillian, eds. Audubon wildlife report 1988/1989. San Diego, CA: Academic Press: 495-512. [14284] 7. Brinkman, Kenneth A.; Roe, Eugene I. 1975. Quaking aspen: silvics and management in the Lake States. Agric. Handb. 486. Washington, DC: U.S. Department of Agriculture, Forest Service. 52 p. [5107] 8. Chadde, Steve; Kay, Charles. 1988. Willows and moose: a study of grazing pressure, Slough Creek exclosure, Montana, 1961-1986. Number 24. Missoula, MT: University of Montana, School of Forestry, Montana Forest and Range Experiment Station. 5 p. [6916] 9. Chandler, Craig; Cheney, Phillip; Thomas, Philip [and others]. 1983. Fire as a natural process in forests. In: Fire in forestry, volume I; forest fire behavior and effects. New York; John Wiley & Sons: 293-393. [614] 10. Child, Kenneth N. 1983. Railways and moose in the central interior of British Columbia: a recurrent management problem. Alces. 19: 118-136. [13898] 11. Costain, Brent. 1989. Habitat use patterns and population trends among Shiras moose in a heavily logged region of northwestern Montana. Missoula, MT: University of Montana. 258 p. Thesis. [13897] 12. Crete, Michel. 1988. Forestry practices in Quebec and Ontario in relation to moose population dynamics. Forestry and wildlife management in the boreal forest--an Ontario workshop; 1987 December 7-9; Thunder Bay, ON. In: The Forestry Chronicle. 1988 June: 246-250. [5119] 13. Cushwa, Charles T.; Coady, John. 1976. Food habits of moose (Alces alces) in Alaska: a preliminary study using rumen contents analysis. Canadian Field-Naturalist. 90: 11-16. [13895] 14. Davis, James L.; Franzmann, Albert W. 1979. Fire-moose-caribou interrelationships: a review and assessment. Proc. North American Moose Conference Workshop. 15: 80-118. [7534] 15. Dodds, Donald G. 1960. Food competition and range relationships of moose and snowshoe hare in Newfoundland. Journal of Wildlife Management. 24: 52-60. [13894] 16. Edwards, Joan. 1985. Effects of herbivory by moose on flower and fruit production of Aralia nudicaulis. Journal of Ecology. 73: 861-868. [13626] 17. Euler, D. 1975. The economic impact of prescribed burning on moose hunting. Journal of Environmental Management. 3: 1-5. [11181] 18. Eyre, F. H., ed. 1980. Forest cover types of the United States and Canada. Washington, DC: Society of American Foresters. 148 p. [905] 19. 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] 20. Gasaway, William C.; DuBois, Stephen D. 1985. Initial response of moose, Alces alces, to a wildfire in interior Alaska. Canadian Field-Naturalist. 99(2): 135-140. [4509] 22. Gordon, Floyd A. 1976. Spring burning in an aspen-conifer stand for maintenance of moose habitat, West Boulder River, Montana. In: Proceedings, Montana Tall Timbers fire ecology conference and Intermountain Fire Research Council fire & land management symposium; 1974 October 8-10; Missoula, MT. No. 14. Tallahassee, FL: Tall Timbers Research STation: 501-538. [13529] 23. Cringan, Alexander Thom. 1957. History, food habits and range requirements of the woodland caribou of continental North America. Transactions, North American Wildlife Conference. 22: 485-501. [15651] 24. Irwin, Larry L. 1975. Deer-moose relationships on a burn in northeastern Minnesota. Journal of Wildlife Management. 39: 653-662. [13892] 25. Kozlowski, T. T.; Ahlgren, C. E., eds. 1974. Fire and ecosystems. New York: Academic Press. 542 p. [1374] 26. 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] 27. LaChapelle, Alain; Messier, Francois; Crete, Michel. 1984. Importance of moose as a black bear food in southwest Quebec. Alces. 20: 79-83. [13899] 28. LeResche, Robert E.; Davis, James L. 1973. Importance of nonbrowse foods to moose on the Kenai Peninsula, Alaska. Journal of Wildlife Management. 37(3): 279-287. [13123] 29. Matchett, Marc R. 1985. Moose-habitat relationships in the Yaak River drainage, northwestern Montana. Missoula, MT: University of Montana. 229 p. Thesis. [13896] 30. McNicol, J. G.; Gilbert, F. F. 1980. Late winter use of upland cutovers by moose. Journal of Wildlife Management. 44(2): 363-371. [4348] 31. Oaks, Wendell R.; Wilson, A. M.; Fraser, Joseph G. 1984. Performance and release of the new cultival "hachita" blue grama and development of a new blue grama cultivar. In: Abstracts--the 37th annual meeting of the Society for Range Management; 1984 February 12-17; Rapid City, SD. Denver, CO: Society for Range Management; 197. Abstract. [1792] 33. Peek, James M.; Scott, Michael D.; Nelson, Louis J.; [and others}. 1982. Role of cover in habitat management for big game in northwestern United States. Transactions, 47th North American Wildlife and Natural Resources Conference. 47: 363-373. [13901] 34. Peterson, Randolph L. 1955. North American moose. Toronto, ON: University of Toronto Press. 280 p. [13900] 35. Phillips, R. L.; Berg, W. E.; Siniff, D. B. 1973. Moose movement patterns and range use in northwestern Minnesota. Journal of Wildlife Management. 37(3): 266-278. [13893] 36. Pierce, John D. 1984. Shiras moose forage selection in relation to browse availability in north-central Idaho. Canadian Journal of Zoology. 62(12): 2404-2409. [12493] 37. Pierce, D. John; Peek, James M. 1984. Moose habitat use and selection patterns in north-central Idaho. Journal of Wildlife Management. 48(4): 1334-1343. [12516] 38. Ritchie, Brent W. 1978. Ecology of moose in Fremont County, Idaho. Wildlife Bulletin No. 7. Boise, ID: Idaho Department of Fish and Game. 33 p. [4482] 39. Rowe, J. S.; Scotter, G. W. 1973. Fire in the boreal forest. Quaternary Research. 3: 444-464. [72] 40. Spencer, David L; Hakala, John B. 1964. Moose and fire on the Kenai. In: Proceedings, 3rd annual Tall Timbers fire ecology conference; 1964 April 9-10; Tallahassee, FL. Tallahassee, FL: Tall Timbers Research Station: 10-33. [5970] 41. Stelfox, J. G.; Lynch, G. M.; McGillis, J. R. 1976. Effects of clearcut logging on wild ungulates in the central Albertan foothills. Forestry Chronicle. April: 65-70. [13506] 42. Thompson, Ian D.; Vukelich, Milan F. 1981. Use of logged habitats in winter by moose cows with calves in northeastern Ontario. Canadian Journal of Zoology. 59(11): 2103-2114. [14283] 43. Timmermann, H. R.; McNicol, J. G. 1988. Moose habitat needs. Forestry and wildlife management in the boreal forest--an Ontario workshop; 1987 December 7-9; Thunder Bay, ON. In: The Forestry Chronicle. 1988 June: 238-245. [5118] 44. Viereck, Leslie A.; Schandelmeier, Linda A. 1980. Effects of fire in Alaska and adjacent Canada--a literature review. BLM-Alaska Tech. Rep. 6. Anchorage, AK: U.S. Department of the Interior, Bureau of Land Mangement, Alaska State Office. 124 p. [7075] 45. Wolff, Jerry O.; Zasada, John C. 1979. Moose habitat and forest succession on the Tanana river floodplain and Yukon-Tanana upland. In: Proceedings, North American Moose Conference and Workshop No 15; [Date of conference unknown]; Kenai, AK. [Place of publication unknown]. [Publisher unknown]. 213-244. [6860] 46. Krefting, Laurtis W. 1974. The ecology of the Isle Royale Moose with special reference to the habitat. Tech. Bull. 297, Forestry Series 15. Minneapolis, MN: University of Minnesota, Agricultural Experiment Station. 75 p. [8678] 47. Peek, James M. 1974. Intial response of moose to a forest fire in northeastern Minnesota. American Midland Naturalist. 91(2): 435-438. [16531] 48. Hansen, H. L.; Krefting, L. W.; Kurmis, V. 1973. The forest of Isle Royale in relation to fire history and wildlife. Tech. Bull. 294; Forestry Series 13. Minneapolis, MN: University of Minnesota, Agricultural Experiment Station. 44 p. [8120] 49. MacCracken, James G.; Viereck, Leslie A. 1990. Browse regrowth and use by moose after fire in interior Alaska. Northwest Science. 64(1): 11-18. [10803] 50. LeResche, R. E.; Bishop, R. H.; Coady, J. W. 1974. Distribution and habitats of moose in Alaska. Le Naturaliste Canadien. 101: 143-178. [15190]

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