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SPECIES: Acer rubrum

Introductory

SPECIES: Acer rubrum
AUTHORSHIP AND CITATION : Tirmenstein, D. A. 1991. Acer rubrum. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: https://www.fs.usda.gov/database/feis/plants/tree/acerub/all.html [].
ABBREVIATION : ACERUB SYNONYMS : Acer rubrum f. tomentosum (Tausch) Siebert & Voss Acer rubrum f. rubrum Acer rubrum f. pallidum [38,86] SCS PLANT CODE : ACRU COMMON NAMES : red maple scarlet maple TAXONOMY : Red maple is a member of the maple family Aceraceae [97]. It exhibits great morphological variation and has been included in a highly variable complex of related taxa [79,97]. The currently accepted scientific name of red maple is Acer rubrum L. [97]. Many varieties and forms have been identified, but most are no longer recognized. The following varieties are commonly recognized [38,86]: Acer rubrum var. drummondii (Hook. & Arn. ex Nutt.) Sarg., Drummond's maple Acer rubrum var. rubrum, red maple Acer rubrum var. trilobum Torr. & Gray ex K. Koch, Carolina maple Red maple hybridizes with silver maple (A. saccharinum) under natural conditions [64]. A hybrid product of this cross has been identified: Acer X freemanii E. Murray, Freeman maple [64]. LIFE FORM : Tree FEDERAL LEGAL STATUS : No special status OTHER STATUS : NO-ENTRY

DISTRIBUTION AND OCCURRENCE

SPECIES: Acer rubrum
GENERAL DISTRIBUTION : Red maple is one of the most widely distributed trees in eastern North America [97]. Its range extends from Newfoundland and Nova Scotia west to southern Ontario, Minnesota, Wisconsin, and Illinois; south through Missouri, eastern Oklahoma, and southern Texas; and east to southern Florida [64]. It is conspicuously absent from the bottomland forests of the Corn Belt in the Prairie Peninsula of the Midwest, the coastal prairies of southern Louisiana and southeastern Texas, and the swamp prairie of the Florida everglades [97]. It is cultivated in Hawaii [102]. ECOSYSTEMS : FRES10 White - red - jack pine FRES11 Spruce - fir FRES13 Loblolly - shortleaf pine FRES14 Oak - pine FRES15 Oak - hickory FRES16 Oak - gum - cypress FRES17 Elm - ash - cottonwood FRES18 Maple - beech - birch FRES19 Aspen - birch STATES : AL AR CT DE FL GA HI IL IN KY LA ME MA MD MI MN MS MO NH NJ NY NC OH OK PA RI SC TN TX VT VA WV WI MB NB NF NS ON PQ BLM PHYSIOGRAPHIC REGIONS : NO-ENTRY KUCHLER PLANT ASSOCIATIONS : K081 Oak savanna K093 Great Lakes spruce - fir forest K095 Great Lakes pine forest K096 Northeastern spruce - fir forest K097 Southeastern spruce - fir forest K098 Northern floodplain forest K099 Maple - basswood forest K100 Oak - hickory forest K101 Elm - ash forest K102 Beech - maple forest K103 Mixed mesophytic forest K104 Appalachian oak forest K106 Northern hardwoods (seral stages) K107 Northern hardwoods - fir forest (seral stages) K108 Northern hardwoods - spruce forest (seral stages) K110 Northeastern oak - pine forest K111 Oak - hickory - pine forest K112 Southern mixed forest K113 Southern floodplain forest SAF COVER TYPES : 5 Balsam fir 12 Black spruce 14 Northern pin oak 16 Aspen 17 Pin cherry 18 Paper birch 19 Gray birch - red maple 20 White pine - northern red oak - red maple 21 Eastern white pine 22 White pine - hemlock 23 Eastern hemlock 24 Hemlock - yellow birch 25 Sugar maple - beech - yellow birch 26 Sugar maple - basswood 27 Sugar maple 28 Black cherry - maple 30 Red spruce - yellow birch 31 Red spruce - sugar maple - beech 32 Red spruce 33 Red spruce - balsam fir 37 Northern white-cedar 38 Tamarack 39 Black ash - American elm - red maple 43 Bear oak 44 Chestnut oak 45 Pitch pine 46 Eastern redcedar 52 White oak - black oak - northern red oak 53 White oak 55 Northern red oak 57 Yellow-poplar 59 Yellow-poplar - white oak - northern red oak 61 River birch - sycamore 62 Silver maple - American elm 63 Cottonwood 65 Pin oak - sweetgum 73 Southern redcedar 74 Cabbage palmetto 75 Shortleaf pine 76 Shortleaf pine - oak 78 Virginia pine - oak 79 Virginia pine 81 Loblolly pine 82 Loblolly pine - hardwood 85 Slash pine - hardwood 87 Sweetgum - yellow-poplar 88 Willow oak - water oak - diamondleaf (laurel) oak 92 Sweetgum - willow oak 93 Sugarberry - American elm - green ash 95 Black willow 96 Overcup oak - water hickory 97 Atlantic white-cedar 98 Pond pine 100 Pondcypress 101 Baldcypress 103 Water tupelo - swamp tupelo 104 Sweetbay - swamp tupelo - redbay 108 Red maple 109 Hawthorne 110 Black oak SRM (RANGELAND) COVER TYPES : NO-ENTRY HABITAT TYPES AND PLANT COMMUNITIES : Red maple occurs as a dominant or codominant in several eastern deciduous forests and deciduous swamp communities with black ash (Fraxinus nigra), yellow birch (Betula alleghaniensis), northern red oak (Quercus rubra), black oak ( Q. velutinus), aspen (Populus tremuloides), and elm (Ulmus spp.). In mesic upland communities of the Southeast, it grows as an overstory dominant with sweetgum (Liquidambar styraciflua) and water oak (Quercus palustris). Red maple has been included as an indicator or dominant in the following community type (cts) and plant association (pas) classifications: Location Classification Authority AL forest cts Golden 1979 MA forest pas Spurr 1956 se MI deciduous swamp cts Barnes 1976 s MI forest cts Hammitt & Barnes 1989 NY forest cts Glitzenstein & others 1990 s ON general veg. cts Smith & others 1975

MANAGEMENT CONSIDERATIONS

SPECIES: Acer rubrum
WOOD PRODUCTS VALUE : Red maple is an important source of sawtimber and pulpwood [42] but is often overlooked as a wood resource [100]. The wood is used for furniture, veneer, pallets, cabinetry, plywood, barrels, crates, flooring, and railroad ties [25,49,62]. IMPORTANCE TO LIVESTOCK AND WILDLIFE : Red maple is browsed by some wildlife species, including white-tailed deer, moose, elk, and snowshoe hare [97]. It is a particularly valuable white-tailed deer browse during the late fall and winter, and is considered an important deer food in New Brunswick, Nova Scotia, Maine, and Minnesota [31,51,60,70,94]. Although red maple is browsed by moose, it is often only lightly used [19]. Irwin [51], however, reported that red maple is an important fall and winter moose browse in parts of northeastern Minnesota. PALATABILITY : Red maple is one of the most palatable white-tailed deer foods in Minnesota [31]; stump sprouts are especially sought out by deer [74,92]. NUTRITIONAL VALUE : The nutrient content of red maple browse varies with the genetic make-up of the individual plant, plant part, position in the crown, phenological development, and geographic location [22,28]. Soil moisture, soil nutrients, fire history, and climatic conditions also influence food value [22,28,29]. COVER VALUE : Maples provide cover for many species of wildlife [78]. The screech owl, pileated woodpecker, and common flicker nest in cavities in many species of maple [44]. Cavities in red maples in river floodplain communities are often well suited for cavity nesters such as the wood duck [36]. Riparian red maple communities provide autumn roosts for blackbirds in central Ohio [75]. VALUE FOR REHABILITATION OF DISTURBED SITES : Red maple can be planted onto many types of disturbed sites. It can be propagated by seed or by various vegetative techniques. Cleaned seed averages approximately 23,000 per pound (51,100/kg). Red maple is reported to be somewhat tolerant of municipal landfill leachates [41]. Seedlings have been observed colonizing strip mine spoils in parts of Maryland, West Virginia, and Florida [45,72], but seedlings transplanted onto strip-mine spoil banks often do poorly [97]. Direct seeding in old-field communities has not been successful [97]. OTHER USES AND VALUES : Red maple is characterized by showy fruits and flowers and colorful fall foliage [25]. Red maple was first cultivated in 1656 [78], and many cultivars are available [23,63,84]. Red maple can be used to make maple syrup, although sugar maple is much more commonly used [55,97. OTHER MANAGEMENT CONSIDERATIONS : Toxicity: Red maple browse is toxic to cattle and horses, particularly during the summer and late fall [5,15,58]. Insects/disease: Loopers, spanworms, the gallmaking maple borer, maple callus borer, Columbian timber borer, and various scale insects are common damaging agents [4,97]. Red maple has experienced periodic declines in past decades. Although the precise pathogens have not been identified, evidence suggests that insects can weaken the trees, making them more vulnerable to decline [4]. Damage: Red maple is tolerant of water-logged soils and flooding [3,6] and is intermediately tolerant of ice damage. Red maple is susceptible to decay after mechanical damage. Butt rot, trunk rot fungi, heart rot, and stem diseases are common in damaged trees; even increment boring can cause result in serious decay. Pollution: Red maple is relatively tolerant of landfill-contaminated gases [6], but ambient air pollution can damage the foliage [57]. Red maple persists in industrially damaged woodlands near Sudbury, Ontario, despite the accumulation of heavy metals in the soil [52]. Chemical control: Red maple is resistant to herbicides and girdling [66,97]. Picloram or cacodylic acid injected directly into the stems can control red maple. Silviculture: Red maple is often poorly regarded as a timber species due to its susceptibility to defects and disease, and poor form of individuals of sprout-clump origin [27]. Red maple usually grows rapidly after heavy cutting or high-grading, and crop tree release may be a low-cost management option [27]. Mechanical thinning of clumps can produce good-quality sawlogs on good sites [26].

BOTANICAL AND ECOLOGICAL CHARACTERISTICS

SPECIES: Acer rubrum
GENERAL BOTANICAL CHARACTERISTICS : Red maple is a deciduous tree that grows 30 to 90 feet (9-28 m) tall and up to 4 feet (1.6 m) in diameter [16,25]. The bark is smooth and gray but darkens and becomes furrowed in narrow ridges with age [16,38]. Twigs are stout and shiny red to grayish brown [49]. The small, fragrant flowers are borne in slender-stalked, drooping, axillary clusters [8,16,24,49]. The fruit is a paired, winged samara, approximately 0.75 inch (1.9 cm) long [49]. Samaras are red, pink, or yellow [38]. RAUNKIAER LIFE FORM : Undisturbed State: Phanerophyte (mesophanerophyte) Burned or Clipped State: Chamaephyte Burned or Clipped State: Hemicryptophyte REGENERATION PROCESSES : Seed: Red maple can bear seed as early as 4 years of age [78] and produces good or better seed crops over most of its range in 1 out of 2 years [39]. Bumper seed crops do occur. Trees are extremely prolific; individual trees 2 to 8 inches (5-20 cm) in diameter commonly produce 12,000 to 91,000 seeds annually, and trees 12 inches (30 cm) in diameter can produce nearly 1,000,000 seeds [1]. Seed is wind dispersed [97]. Seed banking: In parts of Nova Scotia and Minnesota, red maple seed has been found buried at depths of 0 to 6 inches (0-16 cm) [2,61,81], but these seeds are usually not viable [2,61]. Up to 95 percent of viable seed germinates with the first 10 days [1]; some seed survives within the duff and germinates the following year [30,61]. Seedling establishment: Seedbed requirements for red maple are minimal [42], and a bank of persistent seedlings often accumulates beneath a forest canopy [97]. Seedlings may number more than 11,000 per acre (44,534/ha) [69] and can survive for 3 to 5 years under moderate shade [73]. Vegetative regeneration: Red maple sprouts vigorously from the stump, root crown, or "root suckers" after fire or mechanical damage [32,96,97]. Lees [62] observed that at least three generations of stump sprouts can "thrive on the same regenerating root system." Buds located at the base of stems commonly sprout 2 to 6 weeks after the stem is cut [97]. Mroz and others [77] reported that sprouting is generally confined to the root collar. SITE CHARACTERISTICS : Red maple grows throughout throughout much of the deciduous forest of eastern North America and into the fringes of the boreal forest [49]. It occurs on a variety of wet to dry sites in dense woods and in openings [25]. Red maple grows in low, rich woods, along the margins of lakes, marshes, and swamps, in hammocks, wet thickets, and on floodplains and stream terraces [13,17,24,79,82]. Red maple also occurs in drier upland woodlands, low-elevation cove forests, dry sandy plains, and on stable dunes [24,38,96]. Red maple is a common dominant in many forest types and is considered a major species or associate in more that 56 cover types [97]. In much of the Northeast it grows as an overstory dominant only in swamps and other wet sites [65]. Red maple grows in association with more than 70 important tree species. Soils: Red maple does well on a wider range of soil types, textures, moisture regimes, and pH than does any other forest species in North America [97]. It develops best on moist, fertile, loamy soils [27] but also grows on a variety of dry, rocky, upland soils [49]. Red maple grows on soils derived from a variety of parent materials, including granite, shales, slates, gneisses, schists, sandstone, limestone, conlgomerates, and quartzites [97]. It also occurs on a variety of lacustrine sediments, glacial till, and glacial outwash [53]. Elevation: Red maple grows from sea level to 3,000 feet (0-900 m) in elevation [97]. Elevational ranges by geographic location are as follows: Location Elevation Authority s Appalachians up to 5,904 feet (1,800 m) Duncan & Duncan 1988 White Mountains, NH 1,968 to 2,778 feet (600-850 m) Leak & Graber 1974 SUCCESSIONAL STATUS : Red maple is characterized by a wide ecological amplitude and occupies a wide range of successional stages [54,83]. It is moderately tolerant of shade in the North but intolerant of shade in the Piedmont [97]. Red maple commonly grows as a subclimax or mid-seral species [20,97], but characteristics such as vigorous sprouting, prolific seeding, and ability to compete enable it to pioneer on a variety of disturbed sites [54,97]. This tree lives longer than most seral species [97] but generally does not persist in late successional stages [65]. In even-aged stands which develop after clearcutting, red maple is commonly overtopped by faster growing species such as northern red oak [65]. In a few locations in the Southeast, it grows as a climax dominant in wet-site communities [76]. Red maple commonly increases after disturbances such as windthrow, clearcutting, or fire [97]. In many locations, red maple has increased in importance since presettlement times. Dutch elm disease and chestnut blight have led to increases in the number of red maple stems in many stands [97]. In many parts of the East, red maple has increased in gaps resulting from oak decline and gypsy moth infestations [43,65]. SEASONAL DEVELOPMENT : Red maple is one of the first trees to flower in early spring [97]. Specific flowering dates are largely dependent on weather conditions, and latitude and elevation [8,97]. Flowers generally appear several weeks before vegetative buds. Bud break may be affected by soil factors, and is typically delayed for 7 to 10 days on copper-, lead-, and zinc-mineralized sites [9]. Fruit matures in spring before leaf development is complete [39,97]. Generalized fruiting and flowering dates by geographic location are as follows: Location Flowering Fruiting Authority Adirondack Mtns. Apr June Chapman & Bessette 1990 Blue Ridge Mtns. Feb-Mar ---- Wofford 1989 FL Panhandle Jan-Apr ---- Clewell 1985 Gulf & Atlantic Coasts Jan-May ---- Duncan & Duncan 1987 MD Mar-Apr ---- Batra 1985 MA ---- mid May-early June Abbott 1974 MI late Apr-early May ---- Sakai 1990 NC, SC Jan-Mar Apr-July Radford & others 1968 e TN ---- mid-May-early Apr Farmer & Cunningham 1981 TX Feb ---- Simpson 1988 Nova Scotia late Apr-early May ---- Roland & Smith 1969

FIRE ECOLOGY

SPECIES: Acer rubrum
FIRE ECOLOGY OR ADAPTATIONS : Red maple is a common fire type in the Acadian Forest of New Brunswick, where mean fire intervals have been estimated at 370 years [32]. In the New Jersey Pine Barrens, mean fire intervals averaged 20 years in the early 1900's, but due to a variety of factors including fire suppression and increased prescribed burning, now average 65 years [34]. Red maple regeneration in the Pine Barrens is favored in the absence of fire [34]. In upland oak forests of central Pennsylvania fire suppression has led to the replacement of oaks by red maple, beech, black cherry, and sugar maple [71]. Red maple has also increased in the absence of fire throughout much of the Southeast [11]. In parts of the Appalachians, fire suppression has allowed maple stems to grow large enough and develop bark thick enough to enable them to survive fires [47]. As a result, restoration to presettlement conditions would be "a very long-term process" [47]. Red maple sprouts vigorously from the root crown after aboveground vegetation is killed by fire [87]. Seedling establishment may also occur [87]. FIRE REGIMES : Find fire regime information for the plant communities in which this species may occur by entering the species name in the FEIS home page under "Find Fire Regimes". POSTFIRE REGENERATION STRATEGY : survivor species; on-site surviving root crown or caudex off-site colonizer; seed carried by wind; postfire yrs 1 and 2

FIRE EFFECTS

SPECIES: Acer rubrum
IMMEDIATE FIRE EFFECT ON PLANT : Red maple is intolerant of fire; even large individuals can be killed by moderate fires [97]. Postfire mortality is relatively high for saplings, but because bark becomes thicker and more fire-resistant with age, mortality is much lower for sawtimber [98]. The effects of fire also vary with fire severity, season of burn, and various site factors. DISCUSSION AND QUALIFICATION OF FIRE EFFECT : Season of burn: Late spring or early summer burns are most damaging to understory hardwoods such as red maple [48]. A series of consecutive annual late spring and early summer burns killed the rootstocks of progressively more individuals; however, as many as five consecutive annual winter burns had no effect on sprouting ability of top-killed hardwoods [48]. Bark: Bark of red maple is intermediate in resistance to fire [46]. Mean number of seconds required for the cambium to reach 140 degrees (60 deg C) (often considered a lethal temperature) are as follows [46]: Bark thickness Seconds 0.20 inch 20.0 0.30 inch 56.8 0.40 inch 117.6 PLANT RESPONSE TO FIRE : Fire can stimulate sprouting of dormant red maple buds located on the root crown [97]. Trees top-killed by fire often sprout vigorously and assume increased prominence in postfire stands [85]. Seedlings also sprout and may produce dense sprout clumps following fire [93]. Regrowth following fire is often rapid. Regrowth begins during the first month following summer and fall burns, and significant increases in stem density occur by the third and fourth postfire months. Martin [74] observed red maple sprouts 2 weeks after a July fire in Nova Scotia. Red maple establishes through seed from June through August [33]. Postfire increases in stem density commonly promotes red maple's dominance within a stand [68]. DISCUSSION AND QUALIFICATION OF PLANT RESPONSE : Red maple is reportedly common on burned lands in the Maritime Provinces [82], boreal forests on northern Minnesota [12,51,96], and hardwood forests of the Allegheny Mountains [50]. However, it is rarely observed on burned sites in Rhode Island [14] and was reported to be greatly reduced by prescribed fire in northern Indiana woodlands [18]. On the George Washington National Forest, West Virginia, a spring prescribed fire increased red maple density in a mixed-hardwood forest. Average red maple seedling densities before fire and in postfire year 5 were 132 and 368 seedlings/acre, respectively; red maple sprout densities were 1,368 sprouts/acre before and 1,395 sprouts/acre 5 years after the fire. See the Research Paper of Wendel and Smith's [103] study for details on the fire prescription and fire effects on red maple and 6 other tree species.
The following Research Project Summaries provide further information on prescribed
fire use and postfire response of plant community species, including red
maple, that was not available when this species review was originally
written:
FIRE MANAGEMENT CONSIDERATIONS : 
Protein content of red maple commonly increases on burned sites[22].
Low-intensity fires produced increases in protein levels during the
first postfire season, but no increases were noted the following season.
High-intensity fires produced significant increases in protein levels
during both the first and second seasons [22]. Dills [101] reported,
however, that burning had no effect on the nutritive content of red
maple browse.

REFERENCES

SPECIES: Acer rubrum
REFERENCES : 1. Abbott, Herschel G. 1974. Some characteristics of fruitfulness and seed germination in red maple. Tree Planters' Notes. 25(2): 25-27. [12435] 2. Ahlgren, Clifford E. 1979. Buried seed in the forest floor of the Boundary Waters Canoe Area. Minnesota Forestry Research Note No. 271. St. Paul, MN: University of Minnesota, College of Forestry. 4 p. [3459] 3. Ahlgren, Clifford E.; Hansen, Henry L. 1957. Some effects of temporary flooding on coniferous trees. Forestry. 55(9): 647-650. [2924] 4. Allen, Douglas C. 1987. Insects, declines and general health of northern hardwoods: issues relevant to good forest management. In: Nyland, Ralph D., editor. Managing northern hardwoods: Proceedings of a silvicultural symposium; 1986 June 23-25; Syracuse, NY. Faculty of Forestry Miscellaneous Publication No. 13 (ESF 87-002); Society of American Foresters Publication No. 87-03. Syracuse, NY: State University of New York, College of Environmental Science and Forestry: 252-285. [10659] 5. Anon. 1984. Red maple leaves can kill horses. Crops and Soils Magazine. 36(7): 24. [12737] 6. Arthur, J. J.; Leone, I. A.; Flower, F. B. 1981. Flooding and landfill gas effects on red and sugar maples. Journal of Environmental Quality. 10(4): 431-433. [12555] 7. Barnes, Burton V. 1976. Succession in deciduous swamp communities of southeastern Michigan formerly dominated by American elm. Canadian Journal of Botany. 54: 19-24. [4914] 8. Batra, S. W. T. 1985. Red maple (Acer rubrum L.), an important early spring food resource for honey bees and other insects. Journal of the Kansas Entomological Society. 58(1): 169-172. [12666] 9. Bell, R.; Labovitz, M. L.; Sullivan, D. P. 1985. Delay in leaf flush associated with a heavy metal-enriched soil. Economic Geology. 80: 1407-1414. [11014] 10. 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] 11. Blair, Robert M.; Brunett, Louis E. 1976. Phytosociological changes after timber harvest in a southern pine ecosystem. Ecology. 57: 18-32. [9646] 12. Books, David J. 1972. Little Sioux Burn: year two. Naturalist. 23(3&4): 2-7. [11550] 13. Braun, E. Lucy. 1961. The woody plants of Ohio. Columbus, OH: Ohio State University Press. 362 p. [12914] 14. Brown, James H., Jr. 1960. The role of fire in altering the species composition of forests in Rhode Island. Ecology. 41(2): 310-316. [5935] 15. Burrows, George E.; Tyrl, Ronald J.; Rollins, Dale;. [and others]. [n.d.]. Toxic plants of Oklahoma and the Southern Plains. E-868. Stillwater, OK: Oklahoma State University, Cooperative Extension Service. 40 p. [4994] 16. Chapman, William K.; Bessette, Alan E. 1990. Trees and shrubs of the Adirondacks. Utica, NY: North Country Books, Inc. 131 p. [12766] 17. Clewell, Andre F. 1985. Guide to the vascular plants of the Florida Panhandle. Tallahassee, FL: Florida State University Press. 605 p. [13124] 18. Cole, Kenneth L.; Benjamin, Pamela K.; Klick, Kenneth F. 1990. The effects of prescribed burning on oak woods and prairies in the Indiana Dunes. Restoration & Management Notes. 8(1): 37-38. [13552] 19. Cumming, H. G. 1987. Sixteen years of moose browse surveys in Ontario. Alces. 23: 125-156. [8859] 20. Curtis, J. T.; McIntosh, R. P. 1951. An upland forest continuum in the prairie-forest border region of Wisconsin. Ecology. 32: 476-496. [6927] 21. Cypert, Eugene. 1961. The effects of fires in the Okefenokee Swamp in 1954 and 1955. American Midland Naturalist. 66(2): 485-503. [11018] 22. DeWitt, James B.; Derby, James V., Jr. 1955. Changes in nutritive value of browse plants following forest fires. Journal of Wildlife Management. 19(1): 65-70. [7343] 23. Dirr, Michael A. 1981. What do we know about cultivars?. American Nurseryman. 154(6): 16-17, 88. [12569] 24. Duncan, Wilbur H.; Duncan, Marion B. 1988. Trees of the southeastern United States. Athens, GA: The University of Georgia Press. 322 p. [12764] 25. 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] 26. Erdmann, Gayne G. 1987. Methods of commercial thinning in even-aged northern hardwood stands. In: Nyland, Ralph D., editor. Managing northern hardwoods: Proceedings of a silvicultural symposium; 1986 June 23-25; Syracuse, NY. Faculty of Forestry Miscellaneous Publication No. 13 (ESF 87-002); Society of American Foresters Publication No. 87-03. Syracuse, NY: State University of New York, College of Environmental Science and Forestry: 191-210. [10657] 27. Erdmann, Gayne G.; Peterson, Ralph M., Jr.; Oberg, Robert R. 1985. Crown releasing of red maple poles to shorten high-quality sawlog rotations. Canadian Journal of Forest Research. 15(4): 694-700. [12624] 28. Erdmann, Gayne G.; Crow,, Thomas R.; Rauscher, H. Michael. 1988. Foliar nutrient variation and sampling intensity for Acer rubrum trees. Canadian Journal of Forest Research. 18(1): 134-139. [12622] 29. Eyre, F. H., ed. 1980. Forest cover types of the United States and Canada. Washington, DC: Society of American Foresters. 148 p. [905] 30. Farmer, Robert E., Jr.; Cunningham, Maureen. 1981. Seed dormancy of red maple in east Tennessee. Forest Science. 27(3): 446-448. [12440] 31. Fashingbauer, Bernard A.; Moyle, John B. 1963. Nutritive value of red-osier dogwood and mountain maple as deer browse. Minnesota Academy of Science Proceedings. 31(1): 73-77. [9246] 32. Flinn, Marguerite A.; Wein, Ross W. 1977. Depth of underground plant organs and theoretical survival during fire. Canadian Journal of Botany. 55: 2550-2554. [6362] 33. Flinn, Marguerite A.; Wein, Ross W. 1988. Regrowth of forest understory species following seasonal burning. Canadian Journal of Botany. 66: 150-155. [3014] 34. Forman, Richard T. T.; Boerner, Ralph E. 1981. Fire frequency and the pine barrens of New Jersey. Bulletin of the Torrey Botanical Club. 108(1): 34-50. [8645] 35. 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] 36. Gilmer, David S.; Ball, I. J.; Cowardin, Lewis M.; [and others]. 1978. Natural cavities used by wood ducks in north-central Minnesota. Journal of Wildlife Management. 42(2): 288-298. [13749] 37. Glitzenstein, Jeff S.; Canham, Charles D.; McDonnell, Mark J.; Streng, Donna R. 1990. Effects of environment and land-use history on upland forests of the Cary Arboretum, Hudson Valley, New York. Bulletin of the Torrey Botanical Club. 117(2): 106-122. [13301] 38. Godfrey, Robert K. 1988. Trees, shrubs, and woody vines of northern Florida and adjacent Georgia and Alabama. Athens, GA: The University of Georgia Press. 734 p. [10239] 39. Godman, Richard M.; Mattson, Gilbert A. 1976. Seed crops and regeneration problems of 19 species in northeastern Wisconsin. Res. Pap. NC-123. St. Paul, MN: U.S. Department of Agriculture, Forest Service, North Central Forest Experiment Station. 5 p. [3715] 40. Golden, Michael S. 1979. Forest vegetation of the lower Alabama Piedmont. Ecology. 60(4): 770-782. [9643] 41. Gordon, Andrew M.; McBride, Raymond A.; Fisken, Avril J.; Bates, Tom E. 1989. Effect of landfill leachate irrigation on red maple (Acer rubrum L.) and sugar maple (Acer saccharum Marsh.) seedl. growth and foliar nut. conc. Environmental Pollution. 56(4): 327-336. [13004] 42. Haag, Carl L.; Johnson, James E.; Erdmann, Gayne G. 1989. 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