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Introductory

SPECIES: Gaylussacia baccata | Black Huckleberry
ABBREVIATION : GAYBAC SYNONYMS : Gaylussacia resinosa T. & G. [4,5,16] SCS PLANT CODE : GABA COMMON NAMES : black huckleberry huckleberry TAXONOMY : The currently accepted scientific name for black huckleberry is Gaylussacia baccata (Wang.) K. Koch (Ericaceae) [4,5,16]. There are no currently accepted infrataxa. LIFE FORM : Shrub FEDERAL LEGAL STATUS : No special status OTHER STATUS : NO-ENTRY COMPILED BY AND DATE : Jennifer H. Carey, June 1994 LAST REVISED BY AND DATE : NO-ENTRY AUTHORSHIP AND CITATION : Carey, Jennifer H. 1994. Gaylussacia baccata. In: Remainder of Citation

DISTRIBUTION AND OCCURRENCE

SPECIES: Gaylussacia baccata | Black Huckleberry
GENERAL DISTRIBUTION : Black huckleberry occurs in eastern Canada and the northeastern, north-central, and southeastern United States. Its range extends from Newfoundland west to Manitoba; south through Iowa to Louisiana; east to Georgia; and north to New England [4,5,41]. Disjunct populations occur in the Ouachita Mountains in Arkansas [22]. ECOSYSTEMS : FRES10 White - red - jack pine FRES11 Spruce - fir FRES13 Loblolly - shortleaf pine FRES14 Oak - pine FRES15 Oak - hickory STATES : AL AR CT DE GA IL IN IA KY LA ME MD MA MI MN MS MO NH NJ NY NC OH PA RI SC TN VT VA WV WI MB NB NF NS ON PE PQ ADMINISTRATIVE UNITS : ACAD ALPO APIS ASIS BLRI CACO CATO COLO CUGA CUVA DEWA FIIS GATE GWMP GRSM INDU MACA NERI OBRI PIRO ROCR SHEN SLBE VOYA BLM PHYSIOGRAPHIC REGIONS : NO-ENTRY KUCHLER PLANT ASSOCIATIONS : K081 Oak savanna K094 Conifer bog K095 Great Lakes pine forest K100 Oak - hickory forest K104 Appalachian oak forest K110 Northeastern oak - pine forest K111 Oak - hickory - pine forest SAF COVER TYPES : 1 Jack pine 12 Black spruce 13 Black spruce - tamarack 14 Northern pin oak 15 Red pine 20 White pine - northern red oak - red maple 21 Eastern white pine 38 Tamarack 43 Bear oak 44 Chestnut oak 45 Pitch pine 51 White pine - chestnut oak 52 White oak - black oak - northern red oak 75 Shortleaf pine 76 Shortleaf pine - oak 78 Virginia pine - oak 79 Virginia pine 108 Red maple 110 Black oak SRM (RANGELAND) COVER TYPES : NO-ENTRY HABITAT TYPES AND PLANT COMMUNITIES : Black huckleberry occurs in upland pine (Pinus spp.), oak (Quercus spp.), and mixed pine-oak forests, savannas, and barrens [1,9,19,24,37,53,54]. It is native to dwarf pitch pine (Pinus rigida)-oak forests of the New Jersey pine barrens [17]. Black huckleberry is an indicator plant of northern savanna, a forest-prairie transition community in Minnesota and Wisconsin [24]. Black huckleberry occurs in black oak (Q. velutina) savannas in Indiana [37]. Black huckleberry is commonly present or dominant in peatland bog, raised bog, and carr communities [11,14,28,40]. It is present in the lower shrub layer of a wetland shrub community in New York dominated by common mountain-holly (Nemopanthus mucronatus) and highbush cranberry (Vaccinium corymbosum) [28]. Black huckleberry frequently occurs with other ericaceous shrubs including low sweet blueberry (V. angustifolium), hillside blueberry (V. pallidum), mountain-laurel (Kalmia latifolia), sheep-laurel (Kalmia angustifolia), wintergreen (Gaultheria procumbens), bearberry (Arctostaphylos uva-ursi), rhododendrons (Rhododendron spp.), and dangleberry (Gaylussacia frondosa) [1,9,34,40,54]. Other plant associates not previously mentioned include sweetfern (Comptonia peregrina), chokecherry (Prunus virginiana), sumac (Rhus spp.), flowering dogwood (Cornus florida), and eastern hophornbeam (Ostrya virginiana) [19]. Black huckleberry is listed as a dominant, codominant, or indicator species in the following publications: 1. The ecology of peat bogs of the glaciated northeastern United States: a community profile [11] 2. Community classification of the vascular vegetation of a New Hampshire peatland [14] 3. A field guide to eastern forests: North America [24] 4. Ecological communities of New York State [40] 5. The ecology of the rocky heathlands of western Nova Scotia [47] 6. Vegetation of the Great Smoky Mountains [54]

VALUE AND USE

SPECIES: Gaylussacia baccata | Black Huckleberry
WOOD PRODUCTS VALUE : NO-ENTRY IMPORTANCE TO LIVESTOCK AND WILDLIFE : Black huckleberry provides food, shelter, and cover for wildlife. Numerous birds including sharp-tailed grouse, greater prairie chicken, bobwhite quail, wild turkey, mourning dove, catbird, and scarlet tanager eat the berries [19,52]. Black bear, gray fox, and fox squirrel also eat the berries. White-tailed deer, snowshoe hare, and cottontail rabbit browse stems lightly [19,50]. PALATABILITY : Black huckleberry was not highly preferred by white-tailed deer and snowshoe hare [50]. NUTRITIONAL VALUE : NO-ENTRY COVER VALUE : NO-ENTRY VALUE FOR REHABILITATION OF DISTURBED SITES : Black huckleberry is used for erosion control on sterile acidic sites [19]. In Lehigh Gap, Pennsylvania, black huckleberry cover and density were less where soil was contaminated with heavy metals from a nearby smelter than in uncontaminated areas [23]. OTHER USES AND VALUES : Black huckleberry fruits are edible [8]. Black huckleberry is occasionally used in ornamental plantings [19]. MANAGEMENT CONSIDERATIONS : Niering and Goodwin [36] recommend black huckleberry for right-of-way clearings in Connecticut where trees interfere with powerlines. Dense black huckleberry thickets resisted invasion of trees for at least 15 years in a right-of-way from which trees were originally removed by herbicide application [36]. Black huckleberry is recommended for restoration of the native dwarf pitch pine-oak forests of the New Jersey pine barrens. Black huckleberry is a native component of this forest and provides long-term stability, structural diversity, and wildlife benefits [17]. Propagation techniques are described for black huckleberry [19]. Equations for predicting black huckleberry biomass are available [43,44].

BOTANICAL AND ECOLOGICAL CHARACTERISTICS

SPECIES: Gaylussacia baccata | Black Huckleberry
GENERAL BOTANICAL CHARACTERISTICS : Black huckleberry is a native, deciduous, upright shrub with a profusely and stiffly branched dense crown [39,48,52]. At maturity, it reaches 1 to 4 feet (0.3-1.2 m) in height [52]. The fruit is a fleshy drupe containing around 10 seeds [4,52]. Aerial stems arise from branched rhizomes to form extensive black huckleberry clones [33,39]. The stems are usually 12 to 48 inches (30-122 cm) apart on the rhizomes. The woody rhizomes are usually 0.25 to 0.75 inches (0.6-1.9 cm) in diameter, but may be larger. They are generally confined to the humus layer and the top 1 inch (2.5 cm) of soil. If no humus layer exists, rhizomes are 2 to 3 inches (5.1 to 7.6 cm) deep in the soil. Fibrous roots occur at the base of each aerial stem. Larger roots are generally confined to the same layers as the rhizomes, but may extend as deep as 8 inches (20 cm) [27]. RAUNKIAER LIFE FORM : Geophyte REGENERATION PROCESSES : Black huckleberry regenerates by vegetative reproduction and seed. Existing black huckleberry colonies extend their range and reproduce after disturbance primarily by sprouting from rhizomes [19,39]. In the New Jersey pine barrens, black huckleberry averaged 36.2 dormant buds per 3.9 inches (10 cm) of rhizome [31]. Destruction of aboveground stems stimulates sprouting [19,32]. A stem may grow up to 8 inches (20 cm) in height in the first growing season [39]. In a clearing dominated by shrubs, a black huckleberry clone averaged 7.5 inches (19 cm) of radial expansion a year [36]. Although seedlings are rare [19,31,39], black huckleberry may colonize new sites by seed. Fruit production begins when black huckleberry stems are 3 years old [19]. Heavy crops are produced occasionally [41]. Animals eat the berries, thereby dispersing the seeds [19,21]. Black huckleberry may be self sterile [19]. Germination capacity increases with stratification [4,55]. Warm stratification for 30 days followed by incubation at cold temperatures enhances germination [55]. In an oak woods in which black huckleberry dominated the shrub layer, black huckleberry seeds were not found in the seedbank by either germination or visual search methods [42]. SITE CHARACTERISTICS : Black huckleberry grows on a variety of sites from moist woodlands, thickets, and bogs to dry rocky slopes and stable coastal dunes [13,22,41,52]. It grows at sea level and in mountainous sites approaching 4,000 feet (1,220 m) in elevation in the southern Appalachian Mountains [13,54]. Black huckleberry grows in acidic, coarse textured, low nutrient soils which are well drained [1,19,39,53]. It is common on sandy outwash plains of glaciated areas in the northeastern United States [1,53]. Black huckleberry often grows in shallow soils overlying noncalcareous bedrock or hardpan [9,40,47,48]. Because of its requirement for acidic soils, it is rarely found in soil derived from calcareous rock [5]. In heathlands, black huckleberry is associated with pan development [47]. In Nova Scotia, dense black huckleberry communities occupy healthlands where the hardpan is more than 13.8 inches (35 cm) beneath the surface [48]. Black huckleberry occurs in mature, consolidated, ombrotrophic bogs [11,29,41]. In raised bogs along the Bay of Fundy, black huckleberry occupies well-drained, dry sites where the watertable is generally about 16 inches (41 cm) beneath the surface [10]. SUCCESSIONAL STATUS : Facultative Seral Species Black huckleberry invaded stable black oak dunes in Indiana after a humus layer had developed and soils were well leached [37]. Black huckleberry is intermediate in shade tolerance [19,26]. It frequently grows under open pine and oak canopies and forms dense shrub layers in canopy gaps and clearings [26,33,36]. Once established, black huckleberry tolerates deep shade for a short time but growth is inhibited. As spruce (Picea spp.) and fir (Abies spp.) replace pine and oak in the canopy, black huckleberry declines [30]. Shrub-carr communities in central New York which include black huckleberry represent an intermediate stage of succession between wet meadows and wet forests [28]. Once established, dense thickets of black huckleberry resist invasion by trees [30,36,47,48]. With periodic fire, black huckleberry heath communities in Nova Scotia are very stable [47]. SEASONAL DEVELOPMENT : Leaf bud break and flowering of black huckleberry begin as early as May. Flowering continues through June. Fruits begin to mature by the end of July and remain on the plant until September [16,19,39].

FIRE ECOLOGY

SPECIES: Gaylussacia baccata | Black Huckleberry
FIRE ECOLOGY OR ADAPTATIONS : Black huckleberry is fire tolerant. Aboveground parts are destroyed by most fires, but dormant rhizome buds usually survive and sprout [32,39]. Black huckleberry cover either increases, remains the same, or decreases after fire, depending on rhizome depth, fire severity and frequency, and associated plant community [6,30,31,32]. Low-severity fire encourages prolific vegetative reproduction of black huckleberry [30]. However, severe fire that burns the humus layer, where many of the rhizomes are, can reduce or eliminate black huckleberry from a site. Black huckleberry may not recolonize a severely burned site for several decades [32]. Frequent fire usually decreases black huckleberry cover, probably because of inadequate time between fires to replenish root resources [7]. Black huckleberry regeneration after fire is independent of aboveground severity but not belowground severity. Areas that burn frequently may have low levels of humus, so rhizomes grow in the soil and are less vulnerable to fire. For instance, black huckleberry persists in oak-pine barrens which typically experience severe crown fires [12]. Historically, the New Jersey pine barrens burned with severe crown fire every 20 to 25 years [3]. Presently, these areas are burned by low-severity prescribed fires. Changes in black huckleberry densities in pine barrens with the advent of fire management are unreported [31]. POSTFIRE REGENERATION STRATEGY : Rhizomatous shrub, rhizome in soil

FIRE EFFECTS

SPECIES: Gaylussacia baccata | Black Huckleberry
IMMEDIATE FIRE EFFECT ON PLANT : Most fires kill aboveground portions of black huckleberry [31,32]. Buds on unburned, but heated aboveground stems are usually dead, indicating that black huckleberry buds are very sensitive to heat. Moderate-severity or severe fire that burns the humus layer may kill many of the rhizomes, killing the plant [32]. DISCUSSION AND QUALIFICATION OF FIRE EFFECT : NO-ENTRY PLANT RESPONSE TO FIRE : Surviving rhizomes sprout from dormant buds following fire [6,7]. Sprouting depends on the release of hormonally suppressed buds following the death of the dominant aboveground stem [32]. Sprouting of plants top-killed by fire does not differ in vigor from sprouting of clipped plants, indicating that heat is not a factor in stimulating sprouting [32]. A single low-severity fire usually encourages prolific black huckleberry growth [30]. Vigorous black huckleberry thickets with high stem densities arise after low-severity fire [33]. Annual growth of black huckleberry stems increased considerably in the first growing season after a low-severity March fire in the New Jersey pine barrens. The new sprouts formed a closed canopy by August of the same year, but growth rates diminished rapidly the second year [32]. Brayton and Woodwell [6] compared the response of black huckleberry to light and heavy fire damage from a crown fire which occurred in September. The degree of fire damage was measured using several factors including the amount of charcoal in the soil and the amount of litter remaining. At this Long Island, New York, site black huckleberry rhizomes were generally in the humus layer and the top 1 inch (2.5 cm) of the A1 soil horizon. Where heavy damage occurred (a large amount of charcoal, no litter, and no standing shrub stems), black huckleberry sprouts were restricted to rhizomes that were 0.6 to 1.4 inches (1.5-3.5 cm) beneath the soil surface. In areas with light damage, sprouts originated from rhizomes 0 to 0.8 inches (0-2 cm) beneath the soil surface. The postfire density of black huckleberry was 11 stems per square meter in the heavily damaged area and 72 stems per square meter in the lightly damaged area. The authors concluded that fire damaged the perennating buds on rhizomes in the heavily damaged areas [6]. In a south-central New York oak forest, black huckleberry neither increased nor decreased after a single spring fire when compared to adjacent unburned communities [49]. DISCUSSION AND QUALIFICATION OF PLANT RESPONSE : Effects of repeated burning on black huckleberry vary and may depend on plant community and availiability of light. Buell and Cantlon [7] investigated the effects of fire frequency on an upland oak forest in New Jersey with a well-developed shrub layer. Low-severity prescribed fires were conducted in the winter at 1-, 2-, 3-, 4-, 5-, 10-, and 15-year intervals. Black huckleberry showed long-term decline in percent cover at fire intervals of 5 years or less. Black huckleberry had 40 percent cover on unburned control plots and 3 percent cover on plots burned annually for 10 years. In a black oak savanna in Indiana, two plots were prescribed burned: one plot was burned four times in 8 years (3 spring fires and 1 fall fire) and the other plot was burned five times in 8 years (3 spring and 2 fall fires). Black huckleberry decreased from prefire levels with progressive fires [2]. In little bluestem (Schizachyrium scoparium) grasslands in Connecticut with up to 40 percent woody cover of clonal shrubs, black huckleberry increased in cover with annual spring fires that were conducted while plants were still dormant. Cover of an established black huckleberry thicket on one tract increased four times over prefire levels after 12 annual spring fires [35]. The ability of black huckleberry to increase its cover on this site despite the high fire frequency may be related to the high availability of light. Black huckleberry takes advantage of light with vigorous growth [31]. FIRE MANAGEMENT CONSIDERATIONS : In New Jersey, biomass nutrient concentrations of a heath, shrub, and herb vegetative group which included black huckleberry did not differ depending on site fire history. Sites which had burned by wildfire (usually severe) did not differ significantly (P>0.05) from those that had undergone prescribed burning (low-severity) or from the control which had not burned for 53 years. In addition, nutrient levels in the humus were similar among sites despite differing fire histories [3]. Stergas and Adams [45] determined macronutrient concentrations, ash content, heat content, and ash-free heat content for black huckleberry foliage in four different-aged jack pine (Pinus banksiana) stands. Ash content ranged from 4.38 percent to 4.83 percent. Litter depth did not affect black huckleberry stem production or growth after fire or after clipping of stems to simulate fire [32].

REFERENCES

SPECIES: Gaylussacia baccata | Black Huckleberry
REFERENCES : 1. Archambault, Louis; Barnes, Burton V.; Witter, John A. 1989. Ecological species groups of oak ecosystems of southeastern Michigan. Forest Science. 35(4): 1058-1074. [9768] 2. Bacone, John A.; Post, Thomas W. 1987. Effects of prescribed burning on woody & herbaceous vegetation in black oak sand savannas at Hoosier Praire Nature Preserve, Lake Co., Indiana. Proceedings, Indiana Academy of Science. 96: 205-208. [15588] 3. Boerner, Ralph E. J. 1983. Nutrient dynamics of vegetation and detritus following two intensities of fire in the New Jersey pine barrens. Oecologia. 59: 129-134. [8648] 4. Bonner, F. T.; Halls, Lowell K. 1974. Gaylussacia baccata (Wangh.) K.Koch black huckelberry. In: Schopmeyer, C. S., ed. Seeds of woody plants in the United States. Agriculture Handbook No. 450. Washington, DC: U.S. Department of Agriculture, Forest Service: 427-428. [7672] 5. Braun, E. Lucy. 1961. The woody plants of Ohio. Columbus, OH: Ohio State University Press. 362 p. [12914] 6. Brayton, R. D.; Woodwell, G. M. 1966. Effects of ionizing radiation and fire on Gaylussacia baccata and Vaccinium vacillans. American Journal of Botany. 53(8): 816-820. [9074] 7. Buell, Murray F.; Cantlon, John E. 1953. Effects of prescribed burning on ground cover in the New Jersey pine region. Ecology. 34: 520-528. [9262] 8. Chapman, William K.; Bessette, Alan E. 1990. Trees and shrubs of the Adirondacks. Utica, NY: North Country Books, Inc. 131 p. [12766] 9. Christensen, Norman L. 1988. Vegetation of the southeastern Coastal Plain. In: Barbour, Michael G.; Billings, William Dwight, eds. North American terrestrial vegetation. Cambridge: Cambridge University Press: 317-363. [17414] 10. Damman, A. W. H. 1977. Geographical changes in the vegetation pattern of raised bogs in the Bay of Fundy region of Maine and New Brunswick. Vegetatio. 35(3): 137-151. [10158] 11. Damman, Antoni W. H.; French, Thomas W. 1987. The ecology of peat bogs of the glaciated northeastern United States: a community profile. Biological Report 85(7.16). Washington, DC: U.S. Department of the Interior, Fish and Wildlife Service, Research and Development, National Wetlands Research Center. 100 p. [9238] 12. Dosmann, Mark G.; Patterson, William A.; III; Stack, E.; Caljouw, Caren. 1991. Fire regime of a Massachusetts scrub oak-pitch pine barren. In: Proceedings, 17th Tall Timbers fire ecology conference; 1989 May 18-21; Tallahassee, FL. Tallahassee, FL: Tall Timbers Research Station: 409-410. Abstract. [17623] 13. Duncan, Wilbur H.; Duncan, Marion B. 1987. The Smithsonian guide to seaside plants of the Gulf and Atlantic Coasts from Louisiana to Massachusetts, exclusive of lower peninsular Florida. Washington, DC: Smithsonian Institution Press. 409 p. [12906] 14. Dunlop, D. A. 1987. Community classification of the vascular vegetation of a New Hampshire peatland. Rhodora. 89(860): 415-440. [20275] 15. Eyre, F. H., ed. 1980. Forest cover types of the United States and Canada. Washington, DC: Society of American Foresters. 148 p. [905] 16. Fernald, Merritt Lyndon. 1950. Gray's manual of botany. [Corrections supplied by R. C. Rollins]. Portland, OR: Dioscorides Press. 1632 p. (Dudley, Theodore R., gen. ed.; Biosystematics, Floristic & Phylogeny Series; vol. 2). [14935] 17. Fimbel, Robert A.; Kuser, John E. 1993. Restoring the pygmy pine forest of New Jersey's pine barrens. Restoration Ecology. 1(2): 117-129. [22352] 18. 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] 19. Gill, John D.; Healy, William M. 1974. Shrubs and vines for Northeastern wildlife. Gen. Tech. Rep. NE-9. Upper Darby, PA: U.S. Department of Agriculture, Forest Service, Northeastern Forest Experiment Station. 180 p. [6207] 20. Glaser, Paul H. 1992. Raised bogs in eastern North America--regional controls for species richness and floristic assemblages. Journal of Ecology. 80(3): 535-554. [18425] 21. Gorchov, David L. 1987. Sequence of fruit ripening in bird-dispersed plants: consistency among years. Ecology. 68(1): 223-225. [3395] 22. Hunter, Carl G. 1989. Trees, shrubs, and vines of Arkansas. Little Rock, AR: The Ozark Society Foundation. 207 p. [21266] 23. Jordan, Marilyn J. 1975. Effects of zinc smelter emissions and fire on a chestnut-oak woodland. Ecology. 56: 78-91. [3461] 24. Kricher, John C. 1988. A field guide to eastern forests: North America. Peterson Field Guide Series 37. Boston: Houghton Mifflin Company. 368 p. [22677] 25. 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] 26. Kudish, Michael. 1992. Adirondack upland flora: an ecological perspective. Saranac, NY: The Chauncy Press. 320 p. [19376] 27. Laycock, William A. 1967. Distribution of roots and rhizomes in different soil types in the Pine Barrens of New Jersey. Geological Survey Professional Paper 563-C. Washington, DC: U.S. Department of of the Interior, Geological Survey. 29 p. [Hydrology and ecology, Pine Barrens, New Jersey]. [22934] 28. LeBlanc, Cheryl M.; Leopold, Donald J. 1992. Demography and age structure of a central New York shrub-carr 94 years after fire. Bulletin of the Torrey Botanical Club. 119(1): 50-64. [18208] 29. Lynn, Les M.; Karlin, Eric F. 1985. The vegetation of the low-shrub bogs of northern New Jersey and adjacent New York: ecosystems at their southern limit. Bulletin of the Torrey Botanical Club. 112(4): 436-444. [20276] 30. Martin, J. Lynton. 1956. An ecological survey of burned-over forest land in southwestern Nova Scotia. Forestry Chronicle. 32: 313-336. [8932] 31. Matlack, G. R.; Gibson, D. J.; Good, R. E. 1993. Clonal propagation, local disturbance, and the structure of vegetation: Ericaceous shrubs in the Pine Barrens of New Jersey. Biological Conservation. 63: 1-8. [20098] 32. Matlack, Glenn R.; Gibson, David J.; Good, Ralph E. 1993. Regeneration of the shrub Gaylussacia baccata and associated species after low-intensity fire in an Atlantic coastal plain. American Journal of Botany. 80(2): 119-126. [20726] 33. Matlack, G. R.; Good, R. E. 1989. Plant-scale pattern among herbs and shrubs of a fire-dominated coastal plain forest. Vegetatio. 82: 95-103. [9829] 34. Motzkin, Glenn H.; Patterson, William A., III. 1991. Vegetation patterns and basin morphometry of a New England moat bog. Rhodora. 93(876): 307-321. [17360] 35. Niering, William A.; Dreyer, Glenn D. 1989. Effects of prescribed burning on Andropogon scoparius in postagricultural grasslands in Connecticut. American Midland Naturalist. 122: 88-102. [8768] 36. Niering, William A.; Goodwin, Richard H. 1974. Creation of relatively stable shrublands with herbicides: arresting "succession" on rights-of-way and pastureland. Ecology. 55: 784-795. [8744] 37. Olson, Jerry S. 1958. Rates of succession and soil changes on southern Lake Michigan sand dunes. Botanical Gazette. 119(3): 125-170. [10557] 38. Raunkiaer, C. 1934. The life forms of plants and statistical plant geography. Oxford: Clarendon Press. 632 p. [2843] 39. Reiners, W. A. 1965. Ecology of a heath-shrub synusia in the pine barrens of Long Island, New York. Bulletin of the Torrey Botanical Club. 92(6): 448-464. [22835] 40. Reschke, Carol. 1990. Ecological communities of New York State. Latham, NY: New York State Department of Environmental Conservation, New York Natural Heritage Program. 96 p. [21441] 41. Roland, A. E.; Smith, E. C. 1969. The flora of Nova Scotia. Halifax, NS: Nova Scotia Museum. 746 p. [13158] 42. Schiffman, Paula M.; Johnson, W. Carter. 1992. Sparse buried seed bank in a southern Appalachian oak forest: implications for succession. American Midland Naturalist. 127(2): 258-267. [18191] 43. Smith, W. Brad; Brand, Gary J. 1983. Allometric biomass equations for 98 species of herbs, shrubs, and small trees. Res. Note NC-299. St. Paul, MN: U.S. Department of Agriculture, Forest Service, North Central Forest Experiment Station. 8 p. [20785] 44. Stanek, W.; State, D. [n.d.]. Equations predicting primary productivity (biomass) of trees, shrubs and lesser vegetation based on current literature. [Place of publication unknown]: Environment Canada, Forestry Service. 58 p. On file with: U.S. Department of Agriculture, Forest Service, Intermountain Research Station, Fire Sciences Laboratory, Missoula, MT. [20783] 45. Stergas, R. L.; Adams, K. B. 1989. Jack pine barrens in northeastern New York: postfire macronutrient concentrations, heat content, and understory biomass. Canadian Journal of Forest Research. 19: 904-910. [8629] 46. 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] 47. Strang, R. M. 1971. The ecology of the rocky heathlands of western Nova Scotia. In: Proceedings, annual Tall Timbers fire ecology conference; 1970 August 20-21; Fredericton, NB. No. 10. Tallahassee, FL: Tall Timbers Research Station: 287-292. [5466] 48. Strang, R. M. 1972. Ecology and land use of the barrens of western Nova Scotia. Canadian Journal of Forest Research. 2: 276-290. [21381] 49. Swan, Frederick R., Jr. 1970. Post-fire response of four plant communities in south-central New York state. Ecology. 51(6): 1074-1082. [3446] 50. Telfer, Edmund S. 1972. Browse selection by deer and hares. Journal of Wildlife Management. 36(4): 1344-1349. [12455] 51. U.S. Department of Agriculture, Soil Conservation Service. 1982. National list of scientific plant names. Vol. 1. List of plant names. SCS-TP-159. Washington, DC. 416 p. [11573] 52. Vines, Robert A. 1960. Trees, shrubs, and woody vines of the Southwest. Austin, TX: University of Texas Press. 1104 p. [7707] 53. Weatherbee, Pamela B.; Crow, Garrett E. 1992. Natural plant communities of Berkshire County, Massachusetts. Rhodora. 94(878): 171-209. [19726] 54. Whittaker, R. H. 1956. Vegetation of the Great Smoky Mountains. Ecological Monographs. 26(1): 1-79. [11108] 55. Young, James A.; Young, Cheryl G. 1986. Collecting, processing and germinating seeds of wildland plants. Portland, OR: Timber Press. 236 p. [12232]

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