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Introductory

SPECIES: Betula glandulosa | Bog Birch
ABBREVIATION : BETGLA SYNONYMS : Betula glandulosa var. hallii SCS PLANT CODE : BEGL COMMON NAMES : bog birch glandular birch resin birch swamp birch glandular scrub birch ground birch dwarf birch mountain birch marsh birch arctic dwarf birch shrub birch scrub birch TAXONOMY : The currently accepted scientific name of bog birch is Betula glandulosa Michx. [4,25,63]. An abundance of intermediate forms makes a precise distinction between bog birch (Betula glandulosa) and swamp birch (Betula pumila) difficult. This taxonomic uncertainty results in intermediates regarded as either: Betula glandulosa Michx. var. glandulifera (Regel) Gleason [17,23] or Betula pumila L. var. glandulifera Regel [4,25]. This paper recognizes these intermediate forms as Betula pumila var. glandulifera, as more recent authorities do [4,6,25]. However, due to the continued uncertainty over their proper taxonomic placement, information on these plants will be incorporated into this paper, and they will be cited as Betula pumila var. glandulifera. This paper does not recognize any subspecies, varieties, or forms of Betula glandulosa. Numerous hybrids have been described within this group including [4,6]: Betula glandulosa x occidentalis = B. X eastwoodea Sargent Betula glandulosa x pumila var. glandulifera = B. X sargentii Dugle Betula papyrifera x pumila var. glandulifera = B. X sandbergii Britt Betula neoalaskana x pumila var. glandulifera = B. X uliginosa Dugle B. X sargentii x papyrifera = B. X arbuscula Dugle LIFE FORM : Shrub FEDERAL LEGAL STATUS : NO-ENTRY OTHER STATUS : NO-ENTRY COMPILED BY AND DATE : Ronald Uchytil/August 1989 LAST REVISED BY AND DATE : NO-ENTRY AUTHORSHIP AND CITATION : Uchytil, Ronald J. 1989. Betula glandulosa. In: Remainder of Citation

DISTRIBUTION AND OCCURRENCE

SPECIES: Betula glandulosa | Bog Birch
GENERAL DISTRIBUTION : Bog birch is widely distributed from the interior of Alaska across northern Canada to Labrador and Greenland [60]. In the West, it is found from coastal British Columbia in the mountains to California and Colorado [23,63]. In the northeastern United States bog birch is found in Maine and New Hampshire [48]. Betula pumila var. glandulifera inhabits North Dakota, South Dakota, Minnesota, Wisconsin, Michigan, New York, and much of southeastern Canada [4,17,51]. In Idaho, British Columbia, and Alberta both the type specimen of Betula glandulosa and Betula pumila var. glandulifera occur [6]. ECOSYSTEMS : FRES11 Spruce - fir FRES20 Douglas-fir FRES21 Ponderosa pine FRES23 Fir - spruce FRES26 Lodgepole pine FRES44 Alpine STATES : AK CA CO ID ME MT NH OR UT WA WY AB BC MB NF NT NS ON PQ SK YT ADMINISTRATIVE UNITS : CRMO DENA GLAC GRTE LACL NOCA OLYM ROMO TICA VOYA WRST YELL YUCH BLM PHYSIOGRAPHIC REGIONS : 2 Cascade Mountains 4 Sierra Mountains 8 Northern Rocky Mountains 9 Middle Rocky Mountains 10 Wyoming Basin 11 Southern Rocky Mountains 16 Upper Missouri Basin and Broken Lands KUCHLER PLANT ASSOCIATIONS : K008 Lodgepole pine - subalpine forest K012 Douglas-fir forest K015 Western spruce - fir forest K018 Pine - Douglas-fir forest K021 Southwestern spruce - fir forest K037 Mountain mahogany - oak scrub K052 Alpine meadows and barren K093 Great Lakes spruce - forest (B. pumila var. glandulifera) K094 Conifer bog (B. pumila var. glandulifera) SAF COVER TYPES : 12 Black spruce (B. pumila var. glandulifera) 13 Black spruce - tamarack (B. pumila var. glandulifera) 38 Tamarack (B. pumila var. glandulifera) 107 White spruce 201 White spruce 202 White spruce - paper birch 203 Balsam poplar 204 Black spruce 206 Engelmann spruce - subalpine fir 210 Interior Douglas-fir 217 Aspen 218 Lodgepole pine 251 White spruce - aspen 252 Paper birch 253 Black spruce - white spruce 254 Black spruce - paper birch SRM (RANGELAND) COVER TYPES : NO-ENTRY HABITAT TYPES AND PLANT COMMUNITIES : In the boreal forests of interior Alaska and Canada, bog birch is found in many black spruce (Picea mariana) and white spruce (P. glauca) communities and is especially common at the western, northern, and altitudinal limit of trees [44,58,60]. In these northern environments, permafrost prevents the percolation of water, resulting in the development of muskegs, bogs, and ponds which often impede the growth of trees, but which support many low growing shrubs such as bog birch, bog-rosemary (Andromeda polifolia), dwarf arctic birch (Betula nana), and Labrador-tea (Ledum spp.) [14,60]. Over vast areas of the arctic, moist tundra is characterized by continuous and uniformly developed cottongrass (Eriophorum spp.) occasionally interspersed with shrubs including bog birch [60]. Bog birch occurs on these wet sites but may also be found on many cool and dry to mesic spruce sites where it may form a continuous tall shrub layer [14]. Near treeline bog birch often forms extensive pure stands [55] or shrubfields with alders (Alnus spp.) and willows (Salix spp.) [60,61]. In southwestern Canada and the contiguous United States bog birch most often occurs on wetland sites within lodgepole pine (Pinus contorta), Engelmann spruce (Picea engelmanii), or subalpine fir (Abies lasiocarpa) forest types and is often associated with alders and willows [27,29,39,61]. Associated species: In the interior of Alaska and Canada, bog birch is often present in the understory of black and white spruce communities. Commonly associated shrubs throughout the range of this species include grayleaf willow (Salix glauca), Lemmon willow (S. lemmonii), Geyer willow (S. geyerana), Booth willow (S. boothii), thinleaf alder (Alnus incana ssp. tenuifolia), green alder (A. viridis ssp. crispa), prickly rose (Rosa acicularis), Douglas spirea (Spiraea douglasii), bog blueberry (Vaccinium uliginosum), mountain cranberry (V. vitis-idaea), Labrador tea (Ledum groenlandicum), and red-osier dogwood (Cornus sericea) [14,29,39,43,44,61]. Commonly associated grasses and sedges include water sedge (Carex aquatilis), soft-leaved sedge (C. disperma), beaked sedge (C. rostrata), bluejoint reedgrass (Calamagrostis canadensis), and tufted hairgrass (Deschampsia cespitosa) [43,44,63]. Horsetails (Equisetum spp.) and rushes (Juncus spp.) are also often found with bog birch [43,44]. Publications listing bog birch as a dominant, codominant, or indicator species include: Classification, description, and dynamics of plant communities after fire in the taiga of interior Alaska [14] Riparian dominance types of Montana [18] Plant associations of Region Two: Potential plant communities of Wyoming, South Dakota, Nebraska, Colorado, and Kansas [24] Forest vegetation of the Gunnison and parts of the Uncompahgre National Forests: a preliminary habitat type classification [28] Riparian zone associations: Deschutes, Ochoco, Fremont, and Winema National Forests [29] A physical and biological characterization of riparian habitat and its importance to wildlife in Wyoming [39 Wetland community type classification for west-central Montana [43] Ecosystem classification and interpretation of the sub-boreal spruce zone, Prince Rupert Forest Region, British Columbia [44] The Alaska vegetation classification [58]

VALUE AND USE

SPECIES: Betula glandulosa | Bog Birch
WOOD PRODUCTS VALUE : NO-ENTRY IMPORTANCE TO LIVESTOCK AND WILDLIFE : Bog birch is only lightly to moderately browsed by most classes of livestock. Herbage production may be moderate to high in some bog birch communities. However, cattle tend to avoid the boggy soils associated with this species, unless the soil becomes dry enough to walk on, usually in late summer [9,18,29]. Bog birch is eaten by numerous wildlife species. In the Jackson Hole area of Wyoming, it is a preferred browse of many big game animals [1]. Moose, elk, and mule deer consumption may be moderate to heavy in both summer and winter [12,32,33,46,65]. In Alaska, caribou eat the twigs and leaves [60]. In Alaska and Canada, the snowshoe hare feeds heavily on bog birch [50,64]. A study in the Yukon Territories found this birch to be the most preferred browse of snowshoe hares. When the hare population peaked, over 80 percent of available bog birch twigs were eaten during one winter [50]. Bog birch catkins, buds, and seeds are eaten by numerous bird species including ptarmigan, sharp-tailed grouse, spruce grouse, ruffed grouse, redpolls, pine siskin, chickadees, and kinglets [5,36,54,60]. PALATABILITY : The relish and degree of use shown by livestock and wildlife species for bog birch in several western states is rated as follows [1,11,15,42,46,47]. CA CO MT OR WY Cattle poor fair poor poor fair Sheep poor-fair fair fair ---- fair Horses poor poor poor ---- fair Goats poor-fair ---- fair ---- ---- Pronghorn ---- ---- ---- ---- poor Elk ---- ---- poor ---- good Moose ---- ---- good ---- good Mule deer fair ---- poor ---- fair White-tailed deer ---- ---- poor ---- poor Small mammals ---- ---- ---- ---- fair Small nongame birds ---- ---- ---- ---- good Upland game birds ---- ---- ---- ---- fair Waterfowl ---- ---- ---- ---- poor NUTRITIONAL VALUE : Bog birch's energy and protein value is rated as poor [11]. COVER VALUE : Bog birch presumably provides hiding cover for small birds and mammals but is probably of little importance as cover for larger mammals due to its small size. VALUE FOR REHABILITATION OF DISTURBED SITES : This birch does not transplant easily and is of limited use for rehabilitation [26]. OTHER USES AND VALUES : NO-ENTRY MANAGEMENT CONSIDERATIONS : Grazing on wet soils inhabited by bog birch may make sites more susceptible to surface or streambank erosion [29].

BOTANICAL AND ECOLOGICAL CHARACTERISTICS

SPECIES: Betula glandulosa | Bog Birch
GENERAL BOTANICAL CHARACTERISTICS : Throughout much of its range, bog birch is a deciduous, low and spreading to erect shrub, with one to several main stems from 3 to 6.5 feet (1-2 m) tall [4,19,60,63]. The smooth, thin bark is reddish brown, becoming dark gray, and does not peel readily [60]. The twigs have yellowish, crystalline resin glands [60,63]. The 0.4- to 1-inch-long (1-2.5 cm) leaves are nearly orbicular [4]. In the arctic, towards the northern limit of its distribution, bog birch is a prostrate shrub, often less than 8 inches (20 cm) tall [62]. Vegetative reproduction is prevalent in these northern plants and clones often form large continuous mats [22]. Characteristics used to distinguish bog birch (Betula glandulosa) from swamp birch (Betula pumila var. glandulifera) include [6]: B. glandulosa B. pumila var. glandulifera samara wings narrow: (less than 1/2 broad: (greater than 1/2 as as broad as the body) broad as the body) leaves broadly ovate to orbicular, obovate, greater than 10 less than 10 teeth per side teeth per side size generally less than 6.5 feet up to 13.1 feet (4 m) (2 m) chromosomes 2n = 28 B. pumila 2n = 56 RAUNKIAER LIFE FORM : Phanerophyte Chamaephyte REGENERATION PROCESSES : Throughout much of Alaska, Canada, and the contiguous United States, bog birch reproduction is primarily sexual. Plants produce abundant, small seeds which are dispersed by wind. At the northern distributional limit of bog birch, plants rarely produce viable seed and regenerate by vegetative layering [22,62]. Seed production and dispersal: Bog birch plants are monoecious. Male flowers occur in narrow catkins that form in the summer, remain naked until the next spring, and then elongate and shed their pollen. The pistillate catkins appear with the leaves, then become conelike as they mature by late summer or autumn [5]. Most individuals produce numerous catkins which generally contain 30 to 50 winged samara fruits [62]. Each samara contains a single seed. The small seeds average between 3 and 5 million per pound [5]. Samaras are dispersed principally in the fall by wind. During late fall and winter the catkins disintegrate on the shrub, a process which may be aided by the foraging activities of small birds such as chickadees and kinglets [5]. This releases any remaining seed to fall on the snow. Seed has been observed blowing over crusted snow [5]. Any remaining seeds are dispersed in the spring [62]. Germination: Seed that are dispersed in the fall and those that overwinter on the plant are viable [49]. Germination occurs fairly rapidly under normal temperatures after winter stratification [34]. How long bog birch seed remains viable is not known; however, seed of most Alaska shrubs lose their viability if they do not germinate during the first or second growing season [34]. Northern Plants: In the arctic, recruitment of new individuals from seed is almost nonexistent. These northern plants regenerate by vegetative layering; little or no sexual reproduction occurs. Here clones develop by lateral extension of branches beneath the surface moss layer, rooting at nodes, with only short vertical branches extending above the surface vegetation [62]. It is hypothesized that the successful establishment of seed may be restricted by the short growing season of the northern environment [62]. SITE CHARACTERISTICS : Bog birch is typically a wetland species occurring in fens, swamps, bogs (both sphagnum and nonsphagnum), muskegs, moist-to-wet tundra, wet meadows, moist-to-wet basins, and along low gradient streams and lakes [4,18,29,37,43,44,60]. This birch has a very high frost tolerance and is distributed over large areas of permafrost [30]. Permafrost prevents water percolation, which often results in the development of extensive muskegs and bogs. Bog birch has a moderate to high shade tolerance [30] and is found in the understory of many black and white spruce taiga communities of Alaska and Canada [14,55,60]. It is apparently more common within black spruce types than white spruce. Black spruce typically occupies poorly drained sites, such as those underlain by permafrost, which contain a thick mat, often made up of sphagnum mosses (Sphagnum spp.), sedges (Carex spp.), and grasses. Bog birch may be interspersed on moist cottongrass-dominated tundra sites or occur on hummocks in wet tundra sites [60]. On some alpine sites it occasionally occurs in relatively dry rocky habitats [4,27]. Soils: Surface layers often have large accumulations of organic matter. In fens and swamps these are normally peats derived from nonsphagnum mosses and sedges; in bogs peats are normally derived from sphagnum mosses. Floodplain soils may have surface textures of silt, fine sandy loam, or organic loam [29]. Soil-water relationships: Krajina and others [30] reported that the nutritional requirements of bog birch are low and stated that "It prefers soils in which accumulation of acid mor humus forms causes eluviation of nutrients, especially calcium and magnesium, from the uppermost soil horizons." This is consistent with other researchers [37,49] who observed bog birch to be uncommon or lacking in swamps and fens with minerotrophic (rich in minerals and nutrients), poorly drained soils but common in ombrotrophic (low nutrient), acidic bogs. However, Pojar and others [44] found bog birch occurring only in minerotrophic swamps which derived their water as runoff from adjacent mineral uplands high in dissolved ions, but absent from ombrotrophic, acidic, sphagnum-derived peat bogs. Swamp birch (Betula pumila var. glandulifera) has been reported in minerotrophic fens [10,49], weakly minerotrophic swamps [21], and ombrotrophic bogs [8,10]. Swamps, fens, wet meadows, swales, and low gradient streams often flood seasonally. These areas often hold standing water in the spring, and water tables often remain near the soil surface throughout the summer [18,29,43,44]. Elevation: Elevational ranges for western states are presented below [11,19,38,43,63]: from 6,500 to 7,500 feet (1,981-2,286 m) in CA 7,700 to 11,400 feet (1,734-3,475 m) in CO 4,000 to 8,000 feet (1,219-2,438 m) in MT 6,000 to 11,000 feet (1,829-3,354 m) in UT 6,400 to 10,500 feet (1,951-3,201 m) in WY SUCCESSIONAL STATUS : Bog birch is typically found on sites where the water table is kept high from runoff of nearby uplands. Bog birch maintains itself in these moist habitats and appears to be a topoedaphic climax species [35,44]. SEASONAL DEVELOPMENT : Bog birch is a deciduous shrub. The male catkins begin blooming in the spring before or as the leaves expand. After fertilization the female catkins ripen and develop into conelike structures which resemble "miniature spruce cones." The majority of seed are dispersed in the fall. Flowering dates for several western states are presented below [11,41,51]: State Flowering Begins Flowering Flowering Ends AK May-June CO April August ID April June MT June Sept ND Mid-June (B. pumila var. glandulifera) SD Mid-June (B. pumila var. glandulifera) UT July July WY June Aug Fruit ripening dates for the following states are presented below [51,60]: State Fruits reach maturity AK July-August ND August-Sept (B. pumila var. glandulifera) SD August-Sept (B. pumila var. glandulifera)

FIRE ECOLOGY

SPECIES: Betula glandulosa | Bog Birch
FIRE ECOLOGY OR ADAPTATIONS : In the northwestern United States bog birch typically occupies wetland sites which burn infrequently. Many wetland sites cannot carry fires until late in the fall due to the high moisture content of the soil and associated vegetation [7,29]. When aboveground plant parts of bog birch are killed by fire, they often sprout from the base of the stem [34,40]. Information on the importance of off-site windblown seed revegetating burned areas is lacking. However, some seeds from nearby plants probably reach burned sites. In the Alaska taiga, bog birch is found on poorly drained and permafrost underlain sites occupied primarily by black spruce stands, muskegs, and bogs. These types are the most widespread in Alaska and burn the most frequently [55,59]. Most black spruce stands burn at least every 100 years [14]. Fires in black spruce usually kill the overstory trees and consume most of the aboveground vegetation [56]. POSTFIRE REGENERATION STRATEGY : Small shrub, adventitious-bud root crown Initial-offsite colonizer (off-site, initial community)

FIRE EFFECTS

SPECIES: Betula glandulosa | Bog Birch
IMMEDIATE FIRE EFFECT ON PLANT : Intense fires in black spruce types occur following exceptionally dry periods or under dry, windy conditions [56]. Such fires can completely remove organic soil layers and leave the roots of shrubs exposed, thus eliminating the ability of bog birch to resprout from basal buds [34,66]. Most fires, however, do not remove the entire organic soil layer, and bog birch is able to resprout from the base of the stem following these fires. DISCUSSION AND QUALIFICATION OF FIRE EFFECT : NO-ENTRY PLANT RESPONSE TO FIRE : After the removal of aboveground vegetation by fire, bog birch resprouts quickly from the stem base [20,40]. It sprouts best when organic soil layers are not destroyed by fire [20,66]. After wildfires in black spruce forests of interior Alaska bog birch often increases in density (stems/unit area) for the first 5 postfire years due to continued sprouting [14,57]. It may continue to increase in density or cover for 25 to 55 years after the fire [14,56]. As the black spruce canopy develops bog birch density decreases, but it will persist in canopy openings when spruce grows in a clumped arrangement [3,14,56]. On wet sites in the arctic near treeline, repeated fires often result in shrub thickets composed of green alder, willows, and bog birch [55]. DISCUSSION AND QUALIFICATION OF PLANT RESPONSE : NO-ENTRY FIRE MANAGEMENT CONSIDERATIONS : In the contiguous United States, areas occupied by bog birch often act as natural fire breaks due to saturated substrates [18]. However, many sites will carry a fire late in the growing season after soils and vegetation become drier. Along low gradient stream channels, fires may reduce the buffering and filtering capacity of the site during the next year's runnoff, thus increasing the chances of erosion [29].

REFERENCES

SPECIES: Betula glandulosa | Bog Birch
REFERENCES : 1. Beetle, Alan A. 1962. Range survey in Teton County, Wyoming: Part 2. Utilization and condition classes. Bull. 400. Laramie, WY: University of Wyoming, Agricultural Experiment Station. 38 p. [418] 2. 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] 3. Black, R. A.; Bliss, L. C. 1978. Recovery sequence of Picea mariana - Vaccinium uliginosum forests after burning near Inuvik, Northwest Territories, Canada. Canadian Journal of Botany. 56: 2020-2030. [7448] 4. Brayshaw, T. Christopher. 1976. Catkin bearing plants of British Columbia. Occas. Pap. No. 18. Victoria, BC: The British Columbia Provincial Museum. 176 p. [6170] 5. Brinkman, Kenneth A. 1974. Betula L. birch. 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: 252-257. [46] 6. Brunsfeld, S. J.; Johnson, F. D. 1986. Notes on Betula ser. Humiles (Betulaceae) in Idaho. Madrono. 33(2): 147-148. [6987] 7. Crane, Marilyn F. 1982. Fire ecology of Rocky Mountain Region forest habitat types. Final Report Contract No. 43-83X9-1-884. Missoula, MT: U.S. Department of Agriculture, Forest Service, Region 1. 272 p. On file with: U.S. Department of Agriculture, Forest Service, Intermountain Research Station, Fire Sciences Laboratory, Missoula, MT. [5292] 8. Curtis, John T. 1959. The vegetation of Wisconsin. Madison, WI: The University of Wisconsin Press. 657 p. [7116] 9. Dayton, William A. 1931. Important western browse plants. Misc. Publ. 101. Washington, DC: U.S. Department of Agriculture. 214 p. [768] 10. Dirschl, H. J.; Coupland, R. T. 1972. Vegetation patterns and site relationships in the Saskatchewan River Delta. Canadian Journal of Botany. 50: 647-675. [7449] 11. 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] 12. Dorn, Robert D. 1970. Moose and cattle food habits in southwestern Montana. Journal of Wildlife Management. 34(3): 559-564. [6173] 13. Eyre, F. H., ed. 1980. Forest cover types of the United States and Canada. Washington, DC: Society of American Foresters. 148 p. [905] 14. Foote, M. Joan. 1983. Classification, description, and dynamics of plant communities after fire in the taiga of interior Alaska. Res. Pap. PNW-307. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station. 108 p. [7080] 15. Gaffney, William S. 1941. The effects of winter elk browsing, south fork of the Flathead River, Montana. Journal of Wildlife Management. 5(4): 427-453. [5028] 16. 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] 17. Great Plains Flora Association. 1986. Flora of the Great Plains. Lawrence, KS: University Press of Kansas. 1392 p. [1603] 18. 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] 19. Harrington, H. D. 1964. Manual of the plants of Colorado. 2d ed. Chicago: The Swallow Press Inc. 666 p. [6851] 20. Hawkes, Brad C. 1982. Fire history and ecology of forest ecosystems in Kluane National Park. In: Wein, Ross W.; Riewe, Roderick R.; Methven, Ian R., eds. Resources and dynamics of the Boreal Zone; [Date of conference unknown]; Thunder Bay, ON. [Place of publication unknown]. Association of Canadian Universities for Northern Studies: 266-280. [7444] 21. Heinselman, M. L. 1970. Landscape evolution, peatland types and the environment in the Lake Agassiz Peatlands Natural Area, Minnesota. Ecological Monographs. 40(2): 235-261. [8378] 22. Hermanutz, L. A.; Innes, D. J.; Weis, I. M. 1989. Clonal structure of arctic dwarf birch (Betula glandulosa) at its northern limit. American Journal of Botany. 76(5): 755-761. [7346] 23. Hitchcock, C. Leo; Cronquist, Arthur. 1964. Vascular plants of the Pacific Northwest. Part 2: Salicaceae to Saxifragaceae. Seattle, WA: University of Washington Press. 597 p. [1166] 24. Johnston, Barry C. 1987. Plant associations of Region Two: Potential plant communities of Wyoming, South Dakota, Nebraska, Colorado, and Kansas. 4th ed. R2-ECOL-87-2. Lakewood, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Region. 429 p. [3519] 25. 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] 26. Kelly, George W. 1970. A guide to the woody plants of Colorado. Boulder, CO: Pruett Publishing Co. 180 p. [6379] 27. Komarkova, Vera. 1986. Habitat types on selected parts of the Gunnison and Uncompahgre National Forests. Final Report Contract No. 28-K2-234. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Forest and Range Experiment Station. 270 p. [1369] 28. Komarkova, Vera; Alexander, Robert R.; Johnston, Barry C. 1988. Forest vegetation of the Gunnison and parts of the Uncompahgre National Forests: a preliminary habitat type classification. Gen. Tech. Rep. RM-163. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Forest and Range Experiment Station. 65 p. [5798] 29. 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] 30. Krajina, V. J.; Klinka, K.; Worrall, J. 1982. Distribution and ecological characteristics of trees and shrubs of British Columbia. Vancouver, BC: University of British Columbia, Department of Botany and Faculty of Forestry. 131 p. [6728] 31. 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] 32. Kufeld, Roland C. 1973. 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Index

Related categories for Species: Betula glandulosa | Bog Birch

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