Overview

Comprehensive Description

General Description

Herblike shrubs, perennial, rhizomatous, 10–20 cm tall. Rhizomes creeping, slender. Vertical stems slender, unbranched. Leaves opposite, often appearing as a whorl of 6 at terminal node due to compression of internodes, 2 larger and 4 smaller; smaller ones developing from axillary buds of larger leaves; leaves at lower nodes rudimentary; petiole 2–3 mm long; leaf blade obovate to ± diamond-shaped, 3.5-4.8 cm long, 1.5-2.5 cm wide, papery, veins 2 or 3, base cuneate, margin entire, apex shortly acuminate. Inflorescences compound cymes, terminal; bracts white, broadly ovate, 0.8-1.2 cm long, 0.5-1.1 cm wide, with 7 parallel veins. Flowers white, ca. 2 mm in diameter. Calyx tube obovate, ca. 1 mm, densely pubescent with grayish white appressed trichomes; teeth higher than disk. Petals reflexed, creamy white, ovate-lanceolate, 1.5–2 mm. Stamens ca. 1 mm; anthers yellowish white, narrowly ovoid. Style ca. 1 mm, glabrous. Fruit red at maturity, globose, ca. 5 mm in diameter; stones ellipsoid-ovoid.
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Distribution

National Distribution

Canada

Origin: Native

Regularity: Regularly occurring

Currently: Present

Confidence: Confident

United States

Origin: Native

Regularity: Regularly occurring

Currently: Present

Confidence: Confident

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North American distribution of bunchberry. Map courtesy of USDA, NRCS. 2011. The PLANTS Database. National Plant Data Team, Greensboro, NC. 2011, 16 November.

Bunchberry is a widely distributed, partially circumboreal species [151]. In North America, it occurs throughout Canada, Alaska, and other northern US latitudes [298,299]. Bunchberry is much less common and often restricted to cool, moist, and/or high-elevation sites in its southern US range [29,52,74,198,272,299]. As of 1934, the southernmost distribution of bunchberry in the eastern United States was thought to be about 38° 35' in an upper elevation site in the Appalachians [309]. In the 1960s, however, Stevens [268] discovered a disjunct bunchberry population farther south in the Blue Ridge Mountains of Albemarle County, Virginia.

States and provinces (as of 2011) [290]:
United States: AK, CO, CT, IA, ID, IL, IN, MA, MD, ME, MI, MN, MT, ND, NH, NJ, NM, NY, OH, OR, PA, RI, SD, VA, VT, WA, WI, WV, WY
Canada: AB, BC, LB, MB, NB, NF, NS, NT, NU, ON, PE, QC, SK, YT

  • 29. Braun, E. Lucy. 1989. The woody plants of Ohio. Columbus, OH: Ohio State University Press. 362 p. [12914]
  • 52. Cox, Donald D. 2002. Wetlands as ecosystems. In: A naturalist's guide to wetland plants: An ecology for eastern North America. Syracuse, NY: Syracuse University Press: 1-26. [69691]
  • 74. Ferguson, I. K. 1966. The Cornaceae in the southeastern United States. Journal of the Arnold Arboretum. 47: 106-116. [7616]
  • 151. Lackschewitz, Klaus. 1991. Vascular plants of west-central Montana--identification guidebook. Gen. Tech. Rep. INT-227. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Research Station. 648 p. [13798]
  • 268. Stevens, Charles E. 1968. A remarkable disjunct occurrence of Cornus canadensis in the Virginia Blue Ridge. Castanea. 33(3): 247-248. [83933]
  • 272. Strausbaugh, P. D.; Core, Earl L. 1977. Flora of West Virginia. 2nd ed. Morgantown, WV: Seneca Books. 1079 p. [23213]
  • 298. Viereck, Leslie A.; Little, Elbert L., Jr. 1972. Alaska trees and shrubs. Agric. Handb. 410. Washington, DC: U.S. Department of Agriculture, Forest Service. 265 p. [6884]
  • 299. Voss, Edward G. 1985. Michigan flora. Part II. Dicots (Saururaceae--Cornaceae). Bulletin 59. Bloomfield Hills, MI: Cranbrook Institute of Science; Ann Arbor, MI: University of Michigan Herbarium. 724 p. [11472]
  • 309. Wherry, E. T. 1934. Temperature relations of the bunchberry, Cornus canadensis L. Ecology. 15(4): 440-443. [8929]
  • 198. Mohlenbrock, Robert H. 1986. Guide to the vascular flora of Illinois. [Revised edition]. Carbondale, IL: Southern Illinois University Press. 507 p. [17383]
  • 290. U.S. Department of Agriculture, Natural Resources Conservation Service. 2012. PLANTS Database, [Online]. Available: http://plants.usda.gov/. [34262]

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Localities documented in Tropicos sources

Cornus canadensis L.:
Burma (Asia)
Canada (North America)
Greenland (North America)
Japan (Asia)
Russian Federation (Asia)
South Korea (Asia)
United States (North America)
China (Asia)

Note: This information is based on publications available through Tropicos and may not represent the entire distribution. Tropicos does not categorize distributions as native or non-native.
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S Jilin (Changbai Shan) [Japan, Korea, N Myanmar, Russia (Far East); North America].
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Cornus canadensis is occurring in S Jilin (Changbai Shan), Japan, Korea, N Myanmar, Russia (Far East), North America.
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Physical Description

Morphology

Description

More info for the terms: cyme, hardwood, rhizome, swamp

This description covers characteristics that may be relevant to fire ecology and is not meant for identification. Keys for identification are available (e.g., [11,27,124,272,299]). For a description of bunchberry × Lapland cornel hybrids, see Hultén [128].

Aboveground description: Bunchberry is a low-growing, mostly herbaceous perennial that often forms patches or clumps from extensive, creeping rhizomes [124,151,261]. Stems are slender, typically less than 10 inches (25 cm) tall, and somewhat woody at the base [95,222]. Leaves are firm and occur in false whorls of 4 to 7 near the top of stems [95,124,261]. Whorls of 6 leaves are typical of flowering stems; whorls of 4 are typical of sterile stems [169,262,299]. Morphology may be affected by site conditions. In Oneida County, Wisconsin, leaves and shoots of bunchberry were larger and thicker in open-canopy than woodland habitats [14], but in Nova Scotia, leaf thickness, stem thickness, and plant height differences were not consistently correlated with coastal barren, inland forest, or intermediate habitats from 2 sites. However at one site, leaves were thicker at the coastal barrens and inland forest than at the intermediate habitat [159]. Individual bunchberry flowers are very small and occur in a terminal cyme surrounded by 4 showy, petal-like bracts [124,261]. There are typically 10 to 25 flowers per inflorescence [18,95]. Fruits are clusters of small (5-8 mm), 2-seeded, berry-like drupes [124,261,298].

Belowground description: Bunchberry grows laterally along rhizomes, which can grow up to 12 inches (30 cm) a year [103]. Along the shoreline of Douglas Lake in Cheboygan County, Michigan, bunchberry plantlets occurred 7 feet (2 m) apart on a single rhizome [262]. In the same county, primary bunchberry rhizomes excavated near Reese's Swamp were slender (0.2-1 mm in diameter), with a bark-like appearance and texture. The rhizomes were fine but strong [169].

Most bunchberry rhizomes and roots occur 1.6 to 5 inches (4-13 cm) deep. In the Douglas-fir forest zone of southern interior British Columbia, bunchberry roots and rhizomes occurred 2 to 5 inches (5-13 cm) below the mineral soil surface [191]. On sandy sites in central Alberta, maximum bunchberry rooting depths were 3.5 inches (9 cm) and 5 inches (13 cm) below the ground surface in black spruce and jack pine stands, respectively [275]. Along the shoreline of Douglas Lake in Cheboygan County, bunchberry rhizomes occurred beneath more than 4 inches (10 cm) of sand [262]. From a stream bank in Cheboygan, bunchberry rhizomes were removed from a maximum depth of 11.8 inches (30 cm) [169]. At the Acadia Forest Experiment Station in New Brunswick, the average depth of bunchberry rhizomes ranged from 1.6 to 5 inches (4-13 cm). Rhizome depth was evaluated at a variety of sites, which included 3- to 16-year-old clearcuts and undisturbed areas in spruce, balsam fir, hardwood, and mixed forest types. Rhizomes were typically found in the mineral soil layer. Depth of the rhizomes did not appear related to forest type or past disturbance [78]. See Vegetative regeneration for additional descriptions of bunchberry rhizomes.

  • 11. Anderson, J. P. 1959. Flora of Alaska and adjacent parts of Canada. Ames, IA: Iowa State University Press. 543 p. [9928]
  • 14. Armentano, Thomas Vincent. 1973. Population ecology and response to stress of Aster macrophyllus and Cornus canadensis. Chapel Hill, NC: University of North Carolina at Chapel Hill. 211 p. Dissertation. [83945]
  • 18. Barrett, Spencer C.; Helenurm, Kaius. 1987. The reproductive biology of boreal forest herbs. I. Breeding systems and pollination. Canadian Journal of Botany. 65(10): 2036-2046. [6624]
  • 78. Flinn, Marguerite A.; Wein, Ross W. 1977. Depth of underground plant organs and theoretical survival during fire. Canadian Journal of Botany. 55(19): 2550-2554. [6362]
  • 95. Great Plains Flora Association. 1986. Flora of the Great Plains. Lawrence, KS: University Press of Kansas. 1392 p. [1603]
  • 103. Hall, Ivan V.; Sibley, Jack D. 1976. The biology of Canadian weeds. 20. Cornus canadensis L. Canadian Journal of Plant Science. 56(4): 885-892. [83881]
  • 124. Hitchcock, C. Leo; Cronquist, Arthur. 1973. Flora of the Pacific Northwest. Seattle, WA: University of Washington Press. 730 p. [1168]
  • 128. Hulten, Eric. 1968. Flora of Alaska and neighboring territories. Stanford, CA: Stanford University Press. 1008 p. [13403]
  • 151. Lackschewitz, Klaus. 1991. Vascular plants of west-central Montana--identification guidebook. Gen. Tech. Rep. INT-227. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Research Station. 648 p. [13798]
  • 159. Lau, Jennifer H. T. 2009. Phenotypic and genotypic differentiation of plant populations between coastal barrens and forests in Nova Scotia, Canada. Halifax, NS: Saint Mary's University. 85 p. Thesis. [83947]
  • 169. Long-Robinson, Tammy M. 1990. A study of the clonal behavior of Cornus canadensis. Biology 556, Boreal Flora. Pellston, MI: University of Michigan, Biological Station. 18 p. [83948]
  • 191. McLean, Alastair. 1968. Fire resistance of forest species as influenced by root systems. Journal of Range Management. 22(2): 120-122. [1621]
  • 222. Pojar, Jim; MacKinnon, Andy, eds. 1994. Plants of the Pacific Northwest coast: Washington, Oregon, British Columbia and Alaska. Redmond, WA: Lone Pine Publishing. 526 p. [25159]
  • 261. Soper, James H.; Heimburger, Margaret L. 1982. Shrubs of Ontario. Life Sciences Miscellaneous Publications. Toronto, ON: Royal Ontario Museum. 495 p. [12907]
  • 262. Southwick, Alrun K. 1981. Cornus canadensis: A boreal species. Botany 510-Boreal flora. Ann Arbor, MI: University of Michigan. 18 p. [83949]
  • 272. Strausbaugh, P. D.; Core, Earl L. 1977. Flora of West Virginia. 2nd ed. Morgantown, WV: Seneca Books. 1079 p. [23213]
  • 275. Strong, W. L.; LaRoi, G. H. 1986. A strategy for concurrently monitoring the plant water potentials of spatially separate forest ecosystems. Canadian Journal of Forest Research. 16(2): 346-351. [10805]
  • 298. Viereck, Leslie A.; Little, Elbert L., Jr. 1972. Alaska trees and shrubs. Agric. Handb. 410. Washington, DC: U.S. Department of Agriculture, Forest Service. 265 p. [6884]
  • 299. Voss, Edward G. 1985. Michigan flora. Part II. Dicots (Saururaceae--Cornaceae). Bulletin 59. Bloomfield Hills, MI: Cranbrook Institute of Science; Ann Arbor, MI: University of Michigan Herbarium. 724 p. [11472]
  • 27. Booth, W. E.; Wright, J. C. 1962. Flora of Montana: Part II--Dicotyledons.[Revised]. Bozeman, MT: Montana State College, Department of Botany and Bacteriology. 280 p. [47286]

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Description

Herblike shrubs, perennial, rhizomatous, 10–20 cm tall. Rhizomes creeping, slender. Vertical stems slender, unbranched. Leaves opposite, often appearing as a whorl of 6 at terminal node due to compression of internodes, 2 larger and 4 smaller; smaller ones developing from axillary buds of larger leaves; leaves at lower nodes rudimentary; petiole 2–3 mm; leaf blade obovate to ± diamond-shaped, 3.5–4.8 × 1.5–2.5 cm, papery, veins 2 or 3, base cuneate, margin entire, apex shortly acuminate. Inflorescences compound cymes, terminal; bracts white, broadly ovate, 0.8–1.2 × 0.5–1.1 cm, with 7 parallel veins. Flowers white, ca. 2 mm in diam. Calyx tube obovate, ca. 1 mm, densely pubescent with grayish white appressed trichomes; teeth higher than disk. Petals reflexed, creamy white, ovate-lanceolate, 1.5–2 mm. Stamens ca. 1 mm; anthers yellowish white, narrowly ovoid. Style ca. 1 mm, glabrous. Fruit red at maturity, globose, ca. 5 mm in diam.; stones ellipsoid-ovoid. Fl. Jul–Aug, fr. Aug–Sep.
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Diagnostic Description

Synonym

Chamaepericlymenum canadense (Linnaeus) Ascherson & Graebner Cornella canadensis (Linnaeus) Rydberg.
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Ecology

Habitat

Site Characteristics and Plant Communities

More info for the terms: association, bog, climax, constancy, cover, density, duff, fire regime, frequency, hardwood, indicator value, mesic, minerotrophic, natural, peat, peatland, phase, presence, softwood, succession, swamp, taiga, tree, xeric

Site characteristics: Bunchberry typically occurs in coniferous, deciduous, and mixed forests, but can also be found in heathlands, barrens, hummocks, bogs, meadows, and thickets [93,95,151,178,222,241,298]. Bunchberry habitats are typically cool and moist (see Plant communities) and occur from about sea level to 5,000 feet (1,500 m) [145,166,222] or higher [50]. Soils in bunchberry habitats often have a relatively thick organic surface horizon [120,150,168], and bunchberry is sometimes associated with decaying wood [162,261,286]; however, bunchberry tolerates a range of soil types and moisture and nutrient conditions (see Soils).

Throughout its range, bunchberry occupies a variety of habitats. Researchers described a wide ecological amplitude for bunchberry in the sub-boreal spruce zone in British Columbia [300]. In west-central Alberta, bunchberry occupied sites ranging from wet to dry, poor to rich, and from 1,600 feet (500 m) to nearly 6,600 feet (2,000 m) in elevation in the Boreal Mixedwood, Lower and Upper Boreal Cordillera, and Subalpine ecoregions [50]. In the Adirondack Uplands of New York, bunchberry was "prolific" in well-drained, mixedwood forest sites receiving full sun to partial shade but also occurred in poorly drained spruce (Picea spp.) and fir (Abies spp.) forests with dense shade [145]. Bunchberry habitats and site characteristics are also described in Plant communities.

Climate: In northern North America, bunchberry predominantly occupies continental climates that are cold and moist. Average temperatures in the coldest month are below 30 °F (0 °C) and in the warmest month generally exceed 50 °F (10 °C). Monthly precipitation can average 1 inch (30 mm) or more in any season. In bunchberry habitats along the West Coast, temperature ranges are similar to those of continental climates, but precipitation in the summer months typically averages less than 1 inch (30 mm) [217]. After evaluating southeastern habitats within and outside bunchberry's range, one researcher suggests that bunchberry is restricted to northern habitats because of its failure to establish on sites where summer soil temperatures exceed 65 °F (18 °C) [309].

Microclimate preferences and tolerances reported from a portion of bunchberry's western range suggest that bunchberry abundance may be greater on warmer sites in its northern range and cooler sites in its southern range. Bunchberry constancy was high in boreal forests of central and northern Alberta, but its cover was significantly greater at central than northern latitudes (P<0.001) [276]. In the central portion of the Cascade Range in Washington, bunchberry occupied a greater range of habitats on the west than the east side. Because of the rain shadow effect, western forests experience cooler temperatures, higher snow packs, and lower evapotranspiration rates during the growing season. In the winter, western forests are warmer, experience less diurnal temperature fluctuations, and have higher humidity levels than eastern forests [61]. In coniferous forests in the central Cascade Range of Oregon, bunchberry was most important in stands with the coldest environments [318].

Bunchberry may tolerate a smaller range of temperature extremes on exposed sites. In northern Idaho, sharp changes in temperature exposure may have caused the "disappear(ance)" of bunchberry after western white pine (Pinus monticola) stands were clearcut. Nighttime temperatures were 10 °F (6 °C) cooler and daytime temperatures were 10 °F (6 °C) warmer in clearcuts than in uncut forests. Minimum and maximum soil temperatures fluctuated 4 to 5 °F (2-3 °C) in clearcuts and just 1 °F (0.5 °C) in forests. The time between clearcutting and bunchberry's mortality was not reported [157].

Elevation: From the few areas for which bunchberry's elevational range was reported, it appears that ranges are similar (from about sea level to 5,000 feet (1,500 m)) in the Pacific Northwest [166,222] and the Northeast [145]. In west-central Alberta, bunchberry occupied sites ranging from 1,600 feet (500 m) to nearly 6,600 feet (2,000 m) [50]. In western Oregon and Washington, bunchberry was most common at intermediate elevations (2,000-3,500 feet (600-1,000 m)) [265,286]. In the southern Rocky Mountains, bunchberry was restricted to high-elevation sites (7,500 to 11,000 feet (2,300-3,400 m)) [116,186].

Soils: Bunchberry tolerates a variety of soil textures and a range of moisture and nutrient regimes. In west-central Alberta, bunchberry occupied sites ranging from wet to dry and poor to rich [50]. A study of the environmental and phytosociological conditions in deciduous, coniferous, and mixed forests in northwestern New Brunswick reported wide nutrient and moisture tolerances for bunchberry [171]. On Newfoundland islands, bunchberry was common on upland and lowland sites where soils were well-drained to very poorly drained [235]. In Gros Morne National Park, Newfoundland, bunchberry was associated with characteristics found in forested areas, which included limited bare ground, low light availability, and soils with moderate to high moisture levels and carbon to nitrogen ratios, and low pH, magnesium, calcium, and potassium levels [242]. A growing guide reported that bunchberry growth was best in moist but well drained soils that were rich in humus and ranged from very to slightly acidic. Bunchberry also grew in sandy soils when moisture was not limited [263].

Bunchberry occupies sites with a range of moisture regimes. In the Adirondack Uplands of New York, bunchberry was more prolific in mixedwood forests on well-drained soils than in spruce and fir forests on poorly drained soils [145]. In the boreal mixedwoods region of north-central Alberta, bunchberry was most common in the dry to mesic part of the moisture gradient but occurred on sites ranging from xeromesic to hygromesic [148]. In the Great Lakes states, bunchberry was associated with strongly leached, sandy soils, and poorly drained, mineral soils [312]. Bunchberry occurred across the range of dry to wet moisture conditions in 102 boreal conifer-hardwood stands in the northern Great Lakes region. Frequency of bunchberry averaged 61% in dry, 24% in dry-mesic, 24% in mesic, 31% in wet-mesic, and 55% in wet stands [188]. In white spruce-balsam fir (Picea glauca-Abies balsamea) stands on the Keweenaw Peninsula in northern Michigan, bunchberry frequency averaged 15% \in dry-mesic, 53% in mesic, and 30% in wet-mesic stands [189]. In southwestern Manitoba, bunchberry occurred primarily on hummocks and relatively dry microsites in black spruce (P. mariana) swamp peatlands [168].

Bunchberry is tolerant of nutrient poor soils but is not restricted to them. In the boreal mixedwoods region of north-central Alberta, it was most common in nutrient-poor sands, but also occurred in mesotrophic to eutrophic, fine-textured and clay-rich soils [148]. In New Brunswick, bunchberry was often dominant or distinctive in balsam fir forests and red spruce (P. rubens) forests on dry soils with poor to moderately poor nutrient levels [28]. In western Quebec's Lake Abitibi region, the presence of bunchberry often represented nutrient-poor and/or xeric sites [22]. In peatlands in the Bas-Saint-Laurent region of southeastern Quebec, bunchberry was abundant at the edge of peatlands bordering agricultural fields, where conditions were minerotrophic [150]. In wetland ecosystems in northern Lower Michigan, bunchberry occurred almost exclusively in low-light, forest-dominated wetlands with saturated, slightly acidic to neutral, and relatively rich soils [319].

Bunchberry tolerates a range of pH, but is most often described on slightly to very acidic sites (e.g., [242,319]). In the Lake Agassiz Peatlands Natural Area, Minnesota, bunchberry was more plentiful in rich swamp forests where soil pH ranged from 6 to 6.5, than in poor swamp forests where soil pH ranged from 4.5 to 6 [120]. In New York's Adirondack Uplands, bunchberry grew in soils with a pH range of 3.75 to 5.0 [145]. On the Apostle Islands of northern Wisconsin, bunchberry was frequent in pine (Pinus spp.) and wet balsam fir-paper birch (Betula papyrifera) stands where soil pH ranged from 4.2 to 4.8 [20].

Bunchberry grows on both organic and mineral soils but is often described on organic substrates, such as “raw humus” in western Montana [151], coarse woody peat soils in the Great Lakes states [312], peatlands in the Bas-Saint-Laurent region of southeastern Quebec [150], and black spruce swamp peatlands in the southern boreal region of Manitoba where the peat depth averaged 35 inches (90 cm) [168]. In the Lake Agassiz Peatlands Natural Area, bunchberry occurred on peat soils in rich and poor swamp forests [120]. In Berkshire County, Massachusetts, bunchberry occurred in acidic conifer swamps on a thin, peaty surface layer underlain with shallow, rocky mineral soil [304]. In the taiga of interior Alaska, the quaking aspen-black spruce/bunchberry community type occurred on well drained soils with shallow organic layers (about 5 inches (12 cm)) [80].

Coarse woody debris: Bunchberry is often associated with woody material and found growing on and through tree trunks, stumps, and fallen logs [84,222,261]. In cool, moderately moist coniferous forests in western Oregon, bunchberry was common on thick duff or rotted logs [286]. In young, quaking aspen-dominated, boreal forests near Slave Lake, Alberta, bunchberry associated more with logs and stumps classified as decay class 4 or greater than with forest floor. Decay classes ranged from 1 to 7, and larger numbers were associated with increased percentages of air space or softwood and decreased hardness [162].

Plant communities: Throughout northern North America, bunchberry occurs in coniferous, deciduous, and mixed forests [128,240,261]. It is particularly widespread in the understory of spruce and fir forests [17,147,297]. Bunchberry occurred in 88% of 34 white spruce-fir stands and in 96% of 26 black spruce stands distributed from central Alaska to Newfoundland. Sampled stands occurred at sites ranging from 450 to 4,300 feet (140-1,300 m) in elevation [147].

Bunchberry is more commonly associated with conifers than hardwoods [19,240,299]. When mixed forests were surveyed from northern Wisconsin to Nova Scotia, bunchberry was more common beneath eastern hemlock (Tsuga canadensis) than hardwoods [240]. In a large area of northwestern Quebec that included pure quaking aspen, mixed forests, and old-growth northern whitecedar (Thuja occidentalis) forests, bunchberry was associated with low light levels and conifer dominance [19]. However, when researchers surveyed 231 black spruce and quaking aspen stands in northern British Columbia, frequency of bunchberry was nearly equal in black spruce (79%) and quaking aspen (74%) stands [226], and in the Caribou-Poker Creeks Watershed in interior Alaska, bunchberry was more common in quaking aspen-paper birch stands than black spruce stands [287]. In the Anthracite Region of northeastern Pennsylvania, bunchberry was most common in the ecotone between white oak-red maple and eastern hemlock-black spruce communities [64].

Bunchberry's often greater occurrence or abundance in coniferous than deciduous forest types likely relates more to succession than to intrinsic properties of the coniferous or deciduous species. In many of the coniferous forest types where bunchberry is a common or predominant understory species, deciduous species such as alder (Alnus spp.), willow (Salix spp.), birch (Betula spp.), or quaking aspen dominate following fire or other stand-replacing disturbances [80,81,82,231,292]. Although bunchberry cover can be high in young, deciduous stands (<50 years old) [82,257], it is rarely described as a dominant in these stands. Bunchberry is often considered a dominant in mature, coniferous stands but may be less abundant in the early seral stages of conifer stands. Because of the sparse understory in heavily shaded, late-seral forests, bunchberry's dominance may reflect a lack of other understory species more than its absolute abundance or cover.

Bunchberry is commonly recognized as an understory dominant in habitat and community classifications throughout its range [52,80,148,192,221,233,236,283,285]. Because bunchberry is rarely restricted to particular moisture conditions or soil types [167,221,300,315], it is less commonly an indicator species [105,163]. Generally, bunchberry is likely to occur in the understory of cool, temperate and boreal forest types. However, at specific sites or within smaller geographic areas, bunchberry may be more closely associated with particular overstory species and/or site conditions. The discussion below presents community and environmental relationships reported by local studies. This discussion illustrates the range of species and site charactertistics associated with bunchberry, but is not a definitive description of bunchberry habitat, since these studies represent only a small fraction of the community types in which bunchberry is important.

Western North America: Bunchberry is common in montane forests dominated by western hemlock (Tsuga heterophylla), western redcedar (Thuja plicata), and lodgepole pine (Pinus contorta) and in subalpine forests dominated by spruce, fir, and hemlock (Tsuga spp.) [218].

Bunchberry is a common understory species in the following forest cover types recognized by the Society of American Foresters in western North America:

  • white spruce, paper birch, and white spruce-paper birch types in Alaska and western Canada [65,316,317]
  • Pacific silver fir (Abies amabilis)-western hemlock type in the Pacific Northwest [87]
  • western redcedar-western hemlock type in Montana and Idaho and east of the Cascade Range in Oregon, Washington, and southern British Columbia [118]
  • aspen (typically quaking aspen) type across western North America [71]

Alaska, Yukon Territory, and Pacific Northwest: Bunchberry is a typical understory species in coniferous forests of Alaska and northwestern North America. In coastal areas of Alaska, common overstory species include black spruce, white spruce, Sitka spruce (Picea sitchensis), mountain hemlock (Tsuga mertensiana), and western hemlock [48,56,233,289]. In a survey of 129 spruce-dominated forest plots on the Kenai Peninsula, bunchberry occurred in 105 plots [233]. When bogs, forests, and forest-bog ecotones were compared in the southeast Alaska panhandle, bunchberry was chiefly a forest species, but bunchberry × Lapland cornel hybrids were common in the bogs and ecotones [207]. In the taiga of interior Alaska, the quaking aspen-black spruce/bunchberry community type was common on sites burned 60 to 70 years earlier. Stands were typical of warm sites on well-drained soils with shallow organic layers (about 5 inches (12 cm)) [80]. On well-drained uplands in southwestern Yukon Territory and neighboring northern British Columbia, bunchberry was the principal understory species in forb-rich white spruce forests [56]. Along the Alaska Highway in Yukon Territory, bunchberry occurred in spruce and lodgepole pine forest types [214]. In western Alaska, bunchberry was sometimes common in northern rough fescue (Festuca altaica) grasslands [114].

Coniferous forests are the most typical bunchberry habitats in the Pacific Northwest, and associated overstory species include many of those mentioned for Alaska and the Yukon Territory but also include Engelmann spruce (Picea emgelmannii), subalpine fir (Abies lasiocarpa), Pacific silver fir, Douglas-fir (Pseudotsuga menziesii), and Alaska-cedar (Chamaecyparis nootkatensis) [88,119,123,143,264,273]. Bunchberry was a dominant understory species in the following communities:

  • bunchberry phase of the subalpine fir-Oregon boxwood (Paxistima myrsinites) habitat type; an edaphic climax found at 1,200-1,500 feet (370-460 m) on Spodosols or Entisols in the Similkameen Valley [192]
  • western hemlock/Alaska blueberry (Vaccinium alaskensis)/bunchberry association in the cooler, moderately moist part of the western hemlock zone in the Gifford Pinchot National Forest [285]

Bunchberry occupies a wide range of edaphic conditions and forest types in British Columbia. Researchers described a very wide ecological amplitude for bunchberry in the sub-boreal spruce biogeoclimatic zone in British Columbia [300], and in northern British Columbia, bunchberry occurred in nearly all moisture and nutrient regimes within the boreal spruce, sub-boreal spruce, northern Engelmann spruce-subalpine fir, and sub-boreal pine-spruce biogeoclimatic zones [21]. Bunchberry was considered "virtually ubiquitous" in the Engelmann spruce-subalpine fir zone in northwestern British Columbia [221,315]. In the Kamloops Forest region, bunchberry occupied habitats ranging from dry to xeric montane spruce forests to moist and very wet interior western red cedar-western hemlock forests [167]; however, in mature, high-elevation forests in the Engelmann spruce-subalpine fir zone, bunchberry was common on moist or wet sites and only occasional on dry or very dry sites [62]. On the south-central coast of British Columbia, bunchberry was most important in ecotone or transitional forests between coastal fringe forests and inland peatland forests. Transitional forests were dominated by western hemlock and were drier than the inland peatland forests dominated by lodgepole pine [153].

In Washington and Oregon, bunchberry was often described in cool, moist forests. The western hemlock/Alaska blueberry/bunchberry association occurred in the cooler part of the western hemlock zone where moisture conditions were moderately high [285]. Bunchberry was an indicator of moist, cool sites in the western hemlock zone of the Mt Hood National Forest [105]. In Oregon's western Cascade Range, bunchberry was common in old-growth stands dominated by western hemlock, Pacific silver fir, or Alaska-cedar that were generally found on moist, cool sites [66].

Alberta, Manitoba, Idaho, and Montana: Canopy associates within bunchberry habitats in the northern Rockies and northern Plains regions of North America are very similar to those already mentioned. Bunchberry was recognized as a dominant in the following communities:

  • white spruce-balsam fir/bunchberry-twinflower (Linnaea borealis) community type found at 2,300 to 3,600 feet (700-1,100 m) in the highlands of northern Alberta [1]
  • jack pine (Pinus banksiana)/bunchberry community type in lowland areas of the boreal mixedwoods region in north-central Alberta [148]
  • Douglas-fir/bunchberry forest type in the Bear Paw Mountains of north-central Montana [236]

In the highlands of northern Alberta, bunchberry occurred in all 30 surveyed spruce-fir stands but had the greatest cover (up to 32%) in the white spruce-balsam fir/bunchberry-twinflower community type [1]. In lowland areas of north-central Alberta, bunchberry was the diagnostic understory species in the oligo-mesotrophic jack pine/bunchberry community type on relatively dry, low-nutrient sands. It also occurred in white spruce-quaking aspen community types on moister, more nutrient rich, fine-textured soils [148]. On Duck Mountain in southwestern Manitoba, bunchberry occurred primarily on hummocks and drier areas in black spruce swamp peatlands where the peat depth ranged from 16 to 79 inches (40-200 cm) [168]. In early-seral, shrub-dominated communities that established after logging and/or fire in the western redcedar-western hemlock zone of northern Idaho, bunchberry was more abundant on granitic than quartzite soils and was more frequent on north- than south-facing aspects [202]. In the Bear Paw Mountains of north-central Montana, the Douglas-fir/bunchberry forest type is considered the wettest of the Douglas-fir forests [236].

Eastern North America: In eastern North America, bunchberry occurs in coniferous, cold deciduous, and mixed forest types. Overstory associates in these forests typically include black spruce, red spruce, balsam fir, northern whitecedar, jack pine, eastern white pine (P. strobus), quaking aspen, or paper birch [54,55,133,137,187,283,320].

Bunchberry is a common understory species in the following forest cover types recognized by the Society of American Foresters in eastern North America:

  • red spruce-balsam fir and red spruce-yellow birch (Betula alleghaniensis) types from southeastern Quebec and the maritime provinces, south through the Appalachians as far as West Virginia [25,96]
  • balsam fir type in Quebec, the maritime provinces, northern New England, and eastern New York [179]
  • northern whitecedar type in southern Ontario and Quebec, New Brunswick, northern Great Lakes states, New York, and New England [136]
  • eastern hemlock type from southern Ontario to Nova Scotia and south through the Appalachians [311]
  • jack pine-feather moss (Hylocomium spp.) and jack pine-sheep-laurel (Kalmia angustifolia) types which are widespread in Canada, and also found in Great Lakes states, northern New England, and New York [179]
  • paper birch type in the northern coniferous zone of the northeastern United States and eastern Canada [246]
  • aspen type (typically quaking aspen) across Canada and the northern United States; the aspen type is the largest forest type in the Great Lakes states [71]

Eastern Canada: Bunchberry occurs in forests [235], bogs [223], woodlands [82], and blueberry (Vaccinium spp.) crops [103]. In New Brunswick, bunchberry was often dominant or distinctive in balsam fir forests and red spruce forests on dry soils with poor to moderately poor nutrient levels [28]. Bunchberry had the highest indicator value in jack pine stands when the understory vegetation was compared in quaking aspen, paper birch, jack pine, or white spruce-balsam fir forest plots in southwestern Quebec (P<0.0001). Light levels were similar among the forest types [163]. In southeastern Labrador, bunchberry occurred in vegetation types ranging from early-seral paper birch to late-seral fir and spruce. Extensive carpets of bunchberry were described in paper birch stands, and scattered bunchberry was described in fir and spruce stands [84]. On Newfoundland islands, bunchberry was common but had low cover in tamarack (Larix laricina) forests on upland and lowland sites where soils were well-drained to very poorly drained [235].

Great Lakes region: Although bunchberry occurs in a variety of coniferous, deciduous, and mixed forest types [320], it is generally more common in coniferous and mixed forests than in deciduous forests. In the Boundary Waters Canoe Area, bunchberry occurred in upland forest types dominated by black spruce, balsam fir, eastern whitecedar, jack pine, red pine (Pinus resinosa), red maple (Acer rubrum), or quaking aspen. Cover of bunchberry was greatest (3.8-4.5%) in balsam fir-paper birch and black spruce-feather moss stands and least (0.2-0.5%) in jack pine-oak and red maple-quaking aspen-paper birch stands [97]. In Michigan, bunchberry was more frequent in northern boreal forest than in southern deciduous forest [189]. Based on his comprehensive study of Michigan flora, Voss [299] reported that bunchberry often occurred in coniferous forests, mixed forests, swamps, and all but the driest jack pine forests, but rarely occurred in deciduous woodlands [299]. Bunchberry occurred in nearly all forest types in Isle Royale National Park, except for the exclusively deciduous red maple-birch forest. Cover was greatest in paper birch-quaking aspen-white spruce and black spruce-northern whitecedar forest types [113]. When vegetation of Isle Royale National Park was classified and mapped in 1999, bunchberry was considered a distinguishing species in the rare red maple-ash (Fraxinus spp.)-paper birch/bunchberry forest type; however, it was not listed among the most abundant or characteristic understory species for the type. Bunchberry was listed among the characteristic or most abundant understory species in the following forest types:

  • black spruce/Schreber's moss (Pleurozium schreberi)
  • northern whitecedar-(black spruce,balsam fir)/gray alder (Alnus incana)
  • white spruce-balsam fir-quaking aspen/mixed herb
  • northern whitecedar/balsam fir-mountain maple (Acer spicatum)
  • white spruce-balsam fir/Schreber's moss
  • yellow birch-sugar maple (A. saccharum) or white spruce
  • northern whitecedar-yellow birch
  • Canada yew-highbush cranberry-red-osier dogwood-green alder-devil's club (Taxus canadensis-Viburnum edule-Cornus sericea-Alnus viridis-Oplopanax horridus shrubland [283].

In the Great Lakes region, bunchberry occurs on sites that include a range of edaphic conditions, but bunchberry appears to be most common in coniferous stands on sites with mesic moisture regimes. In the Lake Agassiz Peatlands Natural Area, bunchberry was plentiful but had low cover in rich swamp forests and was sparse with very low cover in poor swamp forests. Eastern whitecedar dominated the rich forests on very wet sites where soil pH ranged from 6 to 6.5, and peat depths were 1 to 6 feet (1.8 m). Stunted tamarack was the usual dominant in poor forests on normally saturated sites where soil pH ranged from 4.5 to 6, and peat layers measured 10 to 25 feet (3-8 m) thick [120]. On the Apostle Islands of northern Wisconsin, bunchberry was frequent in pine and wet balsam fir-paper birch stands. In these stands, light levels were high, soil pH ranged from 4.2 to 4.8, and moisture was limited [20]. In a survey of lowland forests in northern Wisconsin, bunchberry's presence was highest in eastern whitecedar-dominated stands that occurred along streams or around springs and lakes with non-stagnant water [39]. In white spruce-balsam fir stands on the Keweenaw Peninsula of northern Michigan, bunchberry frequency averaged 15% in dry-mesic, 53% in mesic, and 30% in wet-mesic stands [189].

New England: Bunchberry was described in coniferous forests, mixed forests, and alpine communities in New England. In Berkshire County, Massachusetts, bunchberry occurred in mesic northern conifer forests and acidic conifer swamps. Swamp soil had a thin peaty surface layer underlain with shallow rocky mineral soil [304]. Bunchberry was also reported in a rare dwarf pitch pine (Pinus rigida) community on Mt Everett in Berkshire County. Harsh edaphic conditions, including shallow, rocky soils, and frequent ice storms were common in the dwarf pitch pine community [201]. Along transects from a stream bank to the center of a bog in Vermont, bunchberry was found within 200 feet (50 m) of the stream but not in the bog. The height and density of black spruce, soil pH, and soil nutrient levels decreased from the stream to bog center. Soil surface water and the water table increased from the stream to bog center [31]. In the central Green Mountains of Vermont, bunchberry was restricted to the red pine/American mountain-ash/bluebead (Sorbus americana/Clintonia borealis) forest type on mesic infertile sites. Bunchberry did not occur in hardwood or eastern hemlock forest types [260]. In the Presidential Range in New Hampshire, bunchberry occurred in alpine vegetation that included dwarf shrublands dominated by blueberries and bog Labrador tea (Ledum groenlandicum) and snow bank communities adjacent to krummholz vegetation at and above timberline [24]. In the Adirondack Uplands of New York, bunchberry was "prolific" in well-drained, mixedwood forests receiving full sun to part shade but also occurred in poorly drained, spruce and fir forests with dense shade [145].

Central Appalachians: At its southernmost distribution in the eastern United States, Albemarle County, Virginia, bunchberry was found beneath clumps of paper birch at 2,700 feet (820 m) on a north-facing slope, which was drier than northern bunchberry habitats [268].

See the Fire Regime Table for a list of plant communities in which bunchberry may occur and information on the FIRE REGIMES associated with those communities.

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  • 264. Spies, Thomas A. 1991. Plant species diversity and occurrence in young, mature, and old-growth Douglas-fir stands in western Oregon and Washington. In: Ruggiero, Leonard F.; Aubry, Keith B.; Carey, Andrew B.; Huff, Mark H., technical coordinators. Wildlife and vegetation of unmanaged Douglas-fir forests. Gen. Tech. Rep. PNW-GTR-285. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Research Station: 111-121. [17309]
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Montane coniferous forests, margins of woods, old tree stumps, mossy areas, open and moist habitats; ca. 1200 m.
Creative Commons Attribution Non Commercial Share Alike 3.0 (CC BY-NC-SA 3.0)

© Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA

Source: Missouri Botanical Garden

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Growing in montane coniferous forests, margins of woods, old tree stumps, mossy areas, open and moist habitats; ca. 1200 m.
Creative Commons Attribution Non Commercial 3.0 (CC BY-NC 3.0)

© Wen, Jun

Source: Plants of Tibet

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Associations

Flower-Visiting Insects of Bunchberry in Illinois

Cornus canadensis (Bunchberry)
(bees suck nectar or collect pollen, flies and beetles suck nectar or feed on pollen, while other insects suck nectar; all observations are from Barrett & Helenurm)

Bees (long-tongued)
Apidae (Bombini): Bombus perplexus, Bombus ternarius, Bombus terricola, Bombus vagans fq, Psithyrus sp. sn; Anthophoridae (Nomadini): Nomada sayi sn; Megachilidae (Osmiini): Osmia proxima

Bees (short-tongued)
Halictidae (Halictinae): Halictus confusus, Lasioglossum spp. fq, Lasioglossum divergens, Lasioglossum quebecensis fq; Halictidae (Sphecodini): Sphecodes spp.; Colletidae (Hylaeinae): Hylaeus basalis; Andrenidae (Andreninae): Andrena miranda, Andrena sigmundi, Andrena w-scripta fq

Wasps
Sphecidae (Crabroninae): Crabro sp. sn; Vespidae (Eumeninae): Ancistrocerus spp. sn

Sawflies
Cimbicidae: Zaraea americana sn

Flies
Syrphidae: Blera badia, Blera confusa, Blera nigripes, Chalcosyrphus curvarius, Chalcosyrphus inarmatus, Chalcosyrphus nemorum, Chalcosyrphus piger, Cheilosia sialia, Mallota posticata, Orthonevra pulchella, Parasyrphus relictus fq, Sphaerophoria bifurcata, Sphaerophoria longipilosa, Syritta pipiens, Syrphus rectus, Temnostoma alternans, Temnostoma balyras, Temnostoma barberi, Tropidia quadrata, Xylota sp., Xylota bigelowi, Xylota hinei; Bombyliidae: Bombylius major, Thevenemyia harrisi; Milichiidae: Paramyia nitens; Muscidae: Eudasyphora cyanicolor, Phaonia serva; Sarcophagidae: Sarcophaga nearctica

Butterflies
Lycaenidae: Celastrina argiolus sn; Pieridae: Pieris napi sn

Beetles
Buprestidae: Anthaxia inornata; Cantharidae: Cantharis sp.; Cerambycidae: Acmaeopsoides rufula, Evodinus monticola monticola, Judolia montivagans montivagans, Pidonia ruficollis fq; Curculionidae: Anthonomus sp., Tychius stepheni; Elateridae: Dalopius sp.; Orsodacnidae: Orsodacne atra; Staphylinidae: Eusphalerum pothos

Plant Bugs
Miridae: Lygus rufidorsus sn

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General Ecology

Fire Management Considerations

More info for the term: fire exclusion

Because bunchberry occurs in recently burned as well as long unburned forests throughout its range, it is unlikely that either frequent fire or fire exclusion would affect bunchberry persistence. Although bunchberry mortality was uncommon on burned sites, severe fires that produce long-duration soil heating or short-duration temperature spikes in the soil could kill bunchberry [77,169]. While mortality on burned-and-logged sites was also uncommon, it was reported after a severe fire left only ash and mineral soil in a clearcut area [67]. So, although it is unlikely that bunchberry would be removed from a site by fire, decreased abundance in the understory is likely following moderate- to high-severity fires [161,295,302].
  • 169. Long-Robinson, Tammy M. 1990. A study of the clonal behavior of Cornus canadensis. Biology 556, Boreal Flora. Pellston, MI: University of Michigan, Biological Station. 18 p. [83948]
  • 67. Dyrness, C. T.; Viereck, L. A.; Foote, M. J.; Zasada, J. C. 1988. The effect on vegetation and soil temperature of logging flood-plain white spruce. Res. Pap. PNW-RP-392. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Research Station. 45 p. [7471]
  • 77. Flinn, Marguerite A.; Pringle, Joan K. 1983. Heat tolerance of rhizomes of several understory species. Canadian Journal of Botany. 61(2): 452-457. [8444]
  • 161. Lee, Philip. 2004. The impact of burn intensity from wildfires on seed and vegetative banks, and emergent understory in aspen-dominated boreal forests. Canadian Journal of Botany. 82(10): 1468-1480. [51462]
  • 295. Viereck, L. A.; Dyrness, C. T. 1979. Ecological effects of the Wickersham Dome fire near Fairbanks, Alaska. Gen. Tech. Rep. PNW-90. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station. 71 p. [6392]
  • 302. Wang, G. Geoff; Kemball, Kevin J. 2005. Effects of fire severity on early development of understory vegetation. Canadian Journal of Forest Research. 35(2): 254-262. [60329]

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Fire Regimes

More info for the terms: climax, fire cycle, fire frequency, fire intensity, fire regime, fire suppression, fire-return interval, frequency, fuel, interference, natural, natural fire rotation, surface fire

Bunchberry occurs in forests with varied presettlement FIRE REGIMES, including those characterized predominantly by stand-replacement fires with long fire-return intervals, such as Sitka spruce-western hemlock forests; those characterized by stand-replacement fires with relatively short fire-return intervals, such as spruce-fir and jack pine forests; and those characterized by surface FIRE REGIMES such as mixed conifer forests (see the Fire Regime Table). In the boreal forests of North America, bunchberry typically persists regardless of fire cycle length [244].

Western North America: In the various forest types that provide bunchberry habitat in the western half of North America, the average fire-return interval can range from 20 to more than 1,000 years. In western Montana, bunchberry occurred in moist lower subalpine, grand fir, western redcedar, and western hemlock forest types, where fires are generally infrequent but severe [75]. In the cedar-hemlock zone of northern Idaho, average fire frequency can range from 25 to more than 500 years. Early-seral forests are more likely to have low-intensity surface fires at shorter intervals compared to late-seral or climax forests, which are more likely to have stand-replacement fires at longer intervals [254]. See the Fire Regime Table for more information on FIRE REGIMES for communities in which bunchberry may occur.

Fire regime information for plant communities in Canada and Alaska where bunchberry is common are not well described in the Fire Regime Table. Fire history was studied on many sites in the Mackenzie Valley, Northwest Territories. Lightning was the most common cause of fire, and lightning fires were common from June to August. Fire size and annual area burned were typically large. The fire regime in a site dominated by mixedwood and pine forests was characterized by surface fires at intervals of 20 to 30 years. Fires became less frequent after about 1925. At a site dominated by black spruce forests, the average fire-return interval was estimated at 80 to 100 years. Nearly all of the study area dominated by black spruce forests burned in the last 180 years except for some high-elevation and floodplain sites. Throughout the Valley, size of the area burned increased northward, but fire frequency did not. Researchers reported that for their record of fires in the Valley from about the mid 1850s to 1973 "there are years with scarcely any fires and years when all hell breaks loose" [245]. Based on pollen and charcoal records, researchers found that 12 large fires burned in the boreal white spruce forests around Rainbow Lake, northeastern Alberta during the past 840 years. The interval between fires ranged from 30 to 130 years, and the average fire-return interval was 69 years [156].

Eastern North America: The average presettlement fire-return interval in forest types that provide bunchberry habitat in eastern North America also ranges from 20 to more than 1,000 years. A 1000-year charcoal record from the Lake of the Clouds in the Boundary Waters Canoe Area indicated that on average, the area's pine- and spruce-dominated forests burned every 70 to 80 years. The range of time between fires, however, ranged from 20 to more than 100 years. There was no evidence that fire frequency had changed much in this area with European settlement, over the past 300 years [280]. However, this was not the case throughout bunchberry's range (see Fire regime changes). In an upland jack pine forest in the boreal region of northwestern Ontario, fire scars recorded 10 major fires from 1848 to 1967 in the Sachigo Hills study area. The shortest period between fires was 5 years and the longest was 30 years [174]. In southern boreal forests along Lake Duparquet in northwestern Quebec, the fire cycle is 100 years (Bergeron 1991 cited in [60]). Quaking aspen, white spruce, and balsam fir are typical in early-seral forests and may persist 200 years, but at about 100 to 150 years after fire, balsam fir and northern white cedar increasingly dominate the overstory [60].

In the studies that described fire behavior in bunchberry habitats in the eastern half of Canada, characteristics ranged from small, patchy fires in boreal forests of interior Labrador [83] to surface fires and active crown fires in jack pine stands in Ontario [271]. From 1870 to 1980, 80 fires burned 21% of the 18,700-mi² (48,500 km²) boreal forest region of interior Labrador. Because the interior region is largely uninhabited wilderness, nearly all fires were ignited by lightning and burned without human interference. In the study area, the fire cycle was slightly greater than 500 years. Growing-season precipitation was lowest during the year in which the largest area burned. Most fires were small and patchy. Fires were more common in open regenerating forests than in mature unburned forests. It was common for only the fringes of dense, mature forests to burn. Although fires occurred from early June to late October, ignitions peaked in late June and early July. Fall fires were often extinguished quickly by rain or snow [83]. Researchers monitored fire behavior during 12 experimental fires in mature jack pine stands with a black spruce understory near Kenshoe Lake, Ontario. Surface fuel loads were moderate in the stands. Fires occurred between late May and early June, when it had been 1 to 15 days since last rain. At the time of the fires, air temperatures ranged from 60 to 85 °F (10-29 °C), relative humidity was 30% to 48%, and wind speeds were 2 to 18 miles (3-29 km)/hour. Fire behavior included surface fires with slow or moderate spread rates and a low frontal fire intensity (<500 kW/m), surface fires with intermittent torching and crowning and moderate intensity (500-3000 kW/m), and active, high-intensity, crown fires (>4000 kW/m). Depth of burn ranged from 0.7 to 2 inches (1.8-5.1 cm) and was greatest for fires that burned after the longest period without rain [271].

Fire regime changes: FIRE REGIMES in many bunchberry habitats have been altered by human settlement, development, and active fire suppression. Reduced fire frequency during the past century was reported in bunchberry habitats in Canada [23], Washington, Oregon [72], and Minnesota [121], but changes are likely not limited to these areas.

When information from literature reviews, contemporary databases, and modeling was used to compare historical (after 1714), current (1959-1999), and predicted future fire frequencies in Canadian boreal forests, researchers found that current fire frequencies were significantly lower than historical. Climate changes and improved fire protection were suggested as the reasons for reduced fire frequency from historic to current times. Historical fire information came from 18 study areas throughout Canada's boreal forest region, and the current fire frequency was estimated from a large Canadian fire database. With modeling, researchers predicted that the relationship between future fire activity and potential changes in climate would vary regionally. Increased temperatures were associated with predictions of increased fire frequency. However, in areas where increased temperatures were combined with increased frequency and amount of precipitation, increased moisture was predicted to moderate the effects of temperature increases so that fire frequency would be unchanged or even decreased [23].

Fire history studies completed in the 1970s in wilderness areas in the Cascade Range of Washington and Oregon suggest that fire frequency decreased between 1910 and 1969. The Pasayten Wilderness in north-central Washington is about 400,000 acres (160,000 ha) and supports a subalpine fir climax forest type. Between 1910 and 1969, the Wilderness averaged 4.5 lightning and 0.6 human-caused fires/year and burned a little less than 100,000 acres. The largest area burned by large fires was from 1920 to 1929, and no area burned in large fires from 1960 to 1969. The last lightning fire that burned more than 1,000 acres (400 ha) occurred in the 1950s. The Mt Jefferson Wilderness in west-central Oregon is about 100,000 acres (40,000 ha) and mostly occurs at elevations over 5,000 feet (1,500 m). Climax forest types are the true fir-mountain hemlock and western hemlock-western redcedar types. Between 1910 and 1969, Mt Jefferson averaged 3 lightning and 1.4 human-caused fires/year and less than 8,000 acres (3,000 ha) burned. All Mt Jefferson fires larger than 40 acres (16 ha) occurred from 1911 to 1924 [72].

From 1542 to 1972 in the Boundary Waters Canoe Area (BWCA), the average time between fire years was 6.1 years, and the average time between large fire years (>100 square miles burned) was 48 years. The natural fire rotation was about 100 years for the BWCA, which is about 800,000 acres (300,000 ha). The time between fires decreased from the presettlement (1727-1868) to settlement period (1868-1910) and increased from the settlement to suppression period (1911-1972). The average fire-return interval in pine stands where at least some trees survived was 36 years but ranged from 5 to 100 years. Large upland ridge sites with jack pine, black spruce, aspen, or birch stand burned most frequently or intensely. Swamps, valleys, ravines, and the east, northeast, north, and southeast sides of large lakes and streams burned least frequently or intensely. In these areas, white pine, red pine, white spruce, and northern white cedar stands were typical [121].

  • 23. Bergeron, Yves; Flannigan, Mike; Gauthier, Sylvie; Leduc, Alain; Lefort, Patrick. 2004. Past, current, and future fire frequency in the Canadian boreal forest: implications for sustainable forest management. Ambio. 33(6): 356-360. [83877]
  • 60. De Grandpre, Louis; Gagnon, Daniel; Bergeron, Yves. 1993. Changes in the understory of Canadian southern boreal forest after fire. Journal of Vegetation Science. 4(6): 803-810. [23019]
  • 72. Fahnestock, George Reeder. 1977. Interactions of forest fire, flora, and fuels in two Cascade Range wilderness areas. Seattle, WA: University of Washington. 179 p. Dissertation. [10431]
  • 75. Fischer, William C.; Bradley, Anne F. 1987. Fire ecology of western Montana forest habitat types. Gen. Tech. Rep. INT-223. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Research Station. 95 p. [633]
  • 83. Foster, David R. 1983. The history and pattern of fire in the boreal forest of southeastern Labrador. Canadian Journal of Botany. 61: 2459-2471. [9683]
  • 121. Heinselman, Miron L. 1973. Fire in the virgin forests of the Boundary Waters Canoe Area, Minnesota. Quaternary Research. 3(3): 329-382. [282]
  • 156. Larsen, C. P. S.; MacDonald, G. M. 1998. An 840-year record of fire and vegetation in a boreal white spruce forest. Ecology. 79(1): 106-118. [28521]
  • 174. Lynham, Timothy J.; Stocks, B. J. 1991. The natural fire regime of an unprotected section of the boreal forest in Canada. In: Proceedings, 17th Tall Timbers fire ecology conference; 1989 May 18-21; Tallahassee, FL. Tallahassee, FL: Tall Timbers Research Station: 99-109. [17602]
  • 244. Rowe, J. S. 1983. Concepts of fire effects on plant individuals and species. In: Wein, Ross W.; MacLean, David A., eds. The role of fire in northern circumpolar ecosystems. SCOPE 18. New York: John Wiley & Sons: 135-154. [2038]
  • 245. Rowe, J. S.; Bergsteinsson, J. L.; Padbury, G. A.; Hermesh, R. 1974. Fire studies in the Mackenzie Valley. ALUR 73-74-61. Ottawa: Canadian Department of Indian and Northern Development. 123 p. [50174]
  • 254. Shiplett, Brian; Neuenschwander, Leon F. 1994. Fire ecology in the cedar-hemlock zone of North Idaho. In: Baumgartner, David M.; Lotan, James E.; Tonn, Jonalea R., compilers. Interior cedar-hemlock-white pine forests: ecology and management: Symposium proceedings; 1993 March 2-4; Spokane, WA. Pullman, WA: Washington State University, Department of Natural Resources: 41-51. [25789]
  • 271. Stocks, B. J. 1989. Fire behavior in mature jack pine. Canadian Journal of Forest Research. 19(6): 783-790. [8672]
  • 280. Swain, Albert M. 1973. A history of fire and vegetation in northeastern Minnesota as recorded in lake sediments. Quaternary Research. 3(3): 383-396. [38931]

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Fuels

More info for the term: fuel

Bunchberry fuel characteristics were not reported in the available literature (2011). In boreal forests, bunchberry is probably unimportant as a fuel that drives or affects fire behavior.

In northeastern Minnesota, bunchberry plants growing in mature forests averaged 270% moisture content from 24 June to 24 July and 237% from 25 July to 26 August. The area experienced a late summer drought. The moisture content of bunchberry was moderate compared to the other 20 understory species evaluated [170].

  • 170. Loomis, Robert M.; Roussopoulos, Peter J.; Blank, Richard W. 1979. Summer moisture contents of understory vegetation in northeastern Minnesota. Res. Pap. NC-179. St. Paul, MN: U.S. Department of Agriculture, Forest Service, North Central Forest Experiment Station. 7 p. [14330]

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Fire adaptations and plant response to fire

More info for the terms: cover, crown fire, density, duff, fire severity, fireline intensity, frequency, fuel, hardwood, high-severity fire, litter, low-severity fire, peat, prescribed fire, ramet, rhizome, severity, succession, surface fire, tree, wildfire

Fire adaptations: Bunchberry survives most fires by sprouting from rhizomes. Postfire seedling establishment on burned sites was not described in the available literature (2011). However, bunchberry seeds may have survived wildfire in a mixed forest stand in northern Saskatchewan where bunchberry was present in the prefire community. Burned soil was collected from plots that burned at severities ranging from light surface fire to crown fire. Fourteen bunchberry stems emerged. Emergents were not identified as developing from remnant vegetative material, as were other emerging species, so they may have developed from seed [13]. Bunchberry seedlings failed to emerge from soil collected immediately after a spring wildfire in quaking aspen stands in northeastern Alberta. A small number of bunchberry seedlings (1.9/m²) did emerge from unburned soil, but none emerged from soil collected from lightly or severely burned plots. Note, however, that seedling emergence studies may underestimate bunchberry seed bank density (see Seed banking) [161]. Bunchberry sprouted after a prescribed fire in white pine-mixed hardwood stands in Strafford County, New Hampshire, but no bunchberry seedlings were observed [37].

Rhizome characteristics: Excavation studies from widely separated regions report that bunchberry rhizomes typically occur about 1.6 to 5 inches (4-13 cm) below the duff or mineral soil surface. For details, see Belowground description.

Bunchberry rhizomes may be killed by temperatures of 100 °F (38 °C) or above, depending on duration of exposure [77,169]. Bunchberry rhizomes collected from an average depth of 3 inches (8 cm) in the Acadian forest type in Nova Scotia that were heated to 113 °F (45 °C) for 5 minutes produced more shoots than unheated rhizomes or rhizomes heated to higher temperatures. Rhizomes heated to 122 °F (50 °C) for 5 minutes also sprouted, but those heated to 131 °F (55 °C) and 140 °F (60 °C) were killed. Rhizomes collected in the fall produced more sprouts after heat treatments than those collected in the spring or summer [77]. This finding may relate to seasonal differences in the levels of total nonstructural carbohydrates, which are greatest in the fall (see Seasonal Development). Bunchberry sprouted after small controlled fires in the Acadian forest conducted in spring, summer, and fall. Temperatures at 0.8 inch (2 cm) into the duff layer reached 131 °F (55 °C) for at least 5 minutes during these fires. In this area, bunchberry rhizomes were found an average of 3 inches (8 cm) below the litter layer and typically grew into mineral soil [79]. Heat was the suspected cause of ramet death after bunchberry clones were excavated from a stream bank in Cheboygan County, Michigan, and transplanted to different environments. All ramets planted outdoors beneath shade cloth or in full sun survived, but all ramets planted in the greenhouse died within 2 weeks of transplanting. Greenhouse temperatures exceeded 100 °F (38 °C) on full-sun days [169].

Plant response to fire: Bunchberry sprouts are common within months of burning, regardless of fire season [37], and increased flower and fruit production have been reported on burned sites ([85], personal observation cited in [280]). Bunchberry may not survive severe fires that produce long-duration soil heating or short-duration temperature spikes in the soil [77,169]. Increases in bunchberry abundance are common after fire; sometimes these increases are immediate [161,243], and other times they are delayed [206,294]. Bunchberry sprouts were "vigorous" after spring and fall prescribed surface fires in white pine-mixed hardwood stands in Strafford County, New Hampshire. Fires did not burn layers beneath the surface litter. Bunchberry failed to flower in the first postfire growing season [37]. Bunchberry cover was greater on 5-year-old burned (15%) than unburned (3%) sites in a mature mixedwood boreal forest near Prince Albert National Park, central Saskatchewan. The wildfire burned understory vegetation but did not penetrate deeply into the organic layer [219]. On Isle Royale, bunchberry was reported on burned sites where the organic layer was not entirely consumed in a balsam fir-paper birch-white spruce stand. The fire burned into the peat layer and killed most trees, but the report did not clearly indicate whether or not bunchberry was restricted to less severely burned areas [47]. Researchers observed bunchberry sprouts 2 months after an August wildfire in 200- to 300-year-old red pine and white pine stands. Based on anecdotal observations, the fire was severe, burned into the canopy, consumed crown foliage, and burned through swamps, marshes, and lowland black spruce stands that often serve as fire breaks. Complete consumption of the organic soil layer was reported in some places [173].

Fire severity: High-severity fires that consume a substantial portion of the duff and litter layers may kill bunchberry plants. Information in the literature is difficult to interpret in regard to fire severity, however, because the studies do not often describe fire severity as it applies to strictly low-growing understory species like bunchberry. In boreal forests, the degree of forest floor consumption by fire can vary with the degree of smoldering that occurs after the fire front has passed, and depth of burn is often unrelated to the intensity of the fire front [301]. For example, in northern conifer forests of the Boundary Waters Canoe Area, an intense crown fire, during a dry spring when wind speeds were high, burned heavy fuel accumulations but rarely consumed the entire duff layer. The following summer, buncherry was common in burned areas [26].

Several studies report postfire occurrence of bunchberry after what they variously describe as high-severity fires. Bunchberry covered large areas 3 to 4 years after a "very severe" summer forest fire near Rangeley Lake, western Maine [259]. Bunchberry was present within a year of a "very severe" fire in a mixedwood forest in Queen's County, Nova Scotia. The fire crossed the study area 3 times before being extinguished [182]. Bunchberry was widespread within 16 months of a crown fire in a white spruce stand in the Agassiz Provincial Forest in Manitoba. The May 1981 fire top-killed all vegetation and consumed the peat layer in many sites within the burned area. No living vegetation was observed in the burned area throughout the remainder of 1981 [126]. Bunchberry occurred within 2 years of an August fire in black spruce forest near Yellowknife, Northwest Territories. The fire was considered "quite severe"; there was persistent smoldering, and "much" mineral soil was exposed [267]. Ten to 11 years after a severe wildfire, which killed nearly all trees in mixed-conifer forest in the Oregon Coast Range, bunchberry was more frequent in adjacent unburned (14%) than severely burned (8%) forest areas [206].

On some sites, bunchberry abundance may be reduced by high-severity crown fires. When the composition and abundance of understory vegetation were compared in 36 deciduous, coniferous, and mixed forest sites that burned lightly, moderately, or severely in an early June wildfire in the northern Clay Belt Region of Quebec, bunchberry was considered an indicator of moderately burned, mixed forests. Lightly burned sites had less than 25% tree mortality, moderately burned sites had 25% to 75% tree mortality, and severely burned sites had more than 75% tree mortality [225]. Bunchberry was described as an understory dominant before a "high-intensity crown fire" in a jack pine-black spruce stand in the Northwest Territories but was not among the understory dominants described in the 2nd or 4th postfire years [125]. Bunchberry responded differently after a late June wildfire in two community types at Wickersham Dome in interior Alaska: black spruce and quaking aspen. The fire consumed the majority of tree crowns and blackened 90% of the understory. In black spruce stands, bunchberry cover and frequency were not much different between unburned and "heavily" burned plots by the 2nd postfire growing season, and they were greater on burned than unburned plots by the 4th postfire growing season. In quaking aspen, however, bunchberry cover was 3.5% to nearly 5% lower on burned than unburned plots in the first 4 postfire growing seasons [295].

Bunchberry abundance was also greater on low-severity than high-severity burns when severity was measured in the ground layer [161,302]. Cover of bunchberry was greater on low-severity burned (7.56%) than high-severity burned (5.65%) and unburned (3.16%) patches 2 years after a spring wildfire in quaking aspen stands in northeastern Alberta. No bunchberry seedlings emerged from low-severity or high-severity burned soils collected immediately after the fire, although seedlings did emerge from unburned soil. Vegetative sprouts emerged from high-severity burned (0.10 sprouts/m²), low-severity burned (0.17 sprouts/m²), and unburned (0.17 sprouts/m²) soil samples. The low-severity fire killed all aboveground plant parts, partially oxidized small and medium-sized downed wood, and consumed 0.8 inch (2 cm) of the organic soil layer. The high-severity fire consumed all aboveground vegetation, oxidized woody material over 8 inches (20 cm) in diameter, and consumed 2 to 4 inches (6-10 cm) of the organic soil layer [161]. When burned plots were evaluated in the first 4 years after a May wildfire in quaking aspen-mixed conifer stands in southeastern Manitoba, average bunchberry cover and frequency were greatest on low-severity burned plots (6.9% and 73%), least on high-severity burned plots (0.9% and 26%), and intermediate on scorched plots (4.3% and 60%) that burned at the lowest severity. The fire was stand replacing, and degree of forest floor consumption was used to classify fire severity. On scorched plots, litter was only partly burned. On low-severity burned plots, litter was burned, but duff consumption was limited. On high-severity burned plots, litter was entirely consumed, and duff was partly consumed [301,302].

Bunchberry recovered to prefire frequencies sooner on low- than high-severity burns in jack pine, spruce-fir, and quaking aspen forest types in Minnesota's Superior National Forest. Time since fire varied from 4 months to 5 years. On severely burned plots, all foliage, small branches (≥0.5 inch (1.3 cm) in diameter), litter, and duff were consumed, and mineral soil was exposed. On lightly burned plots, only loose litter was consumed, and crown scorch was slight. Bunchberry frequency averaged 90% to 93% on 2 unburned sites, 67% on a 2-year-old, severely burned site, and 97% on the 5-year-old, severely burned site. Frequency averaged 97% to 100% on 4-month old, lightly burned plots [4].

In a beetle-attacked Lutz spruce (Picea × lutzii) stand in the Chugach National Forest in south-central Alaska, bunchberry was less abundant 7 years after a June prescribed fire than 4 years before the fire, but it also decreased on unburned plots. Most living and beetle-killed trees were still standing at the time of the fire. All aboveground overstory and understory vegetation was top-killed in the fire, and mineral soil was exposed in spots [127].

Frequency and cover of bunchberry on burned and unburned plots evaluated before and after a prescribed fire in Alaska [127]
Time of evaluation Burned Unburned
Frequency Cover Frequency Cover
Before fire (4 yrs) 59 15 54 8
After fire (7 yrs) 47 9 23 6

Fire season: The few studies that evaluated the effects of different fire seasons in bunchberry habitats suggest that growing-season fires may impact bunchberry populations more severely than dormant-season fires. In mixed conifer-hardwood forests in Minnesota's Superior National Forest, the frequency of bunchberry on summer-burned plots did not reach that of unburned plots by the 11th postfire year, but on spring-burned plots the frequency of bunchberry exceeded unburned levels by the 3rd postfire year. The spring fire burned in late April when the ground was cold and moist and winds were strong and burned little, if any, of the duff layer. The summer fire burned in July, and although it was described as "hot", there was little to no duff consumption [144]. In jack pine stands in northeastern Minnesota, bunchberry occurred in the first postfire growing season after a spring wildfire (14 May) but not after a summer wildfire (27 July). However, prefire comparisons were lacking, so it is unclear whether or not the summer fire killed bunchberry plants. Surface-fire severity was greater in stands burned in the summer where virtually all litter and duff was consumed. The spring fire consumed primarily the litter layer. Both fires burned during dry, windy (23-49 feet (7-15 m)/s) conditions and resulted in "intense" crowning. Average bunchberry biomass ranged from less than 0.1 to 4.1 g/m² and density ranged from 0.2 to 44.8 stems/m² in spring-burned stands. Bunchberry was not reported in either of the 2 summer-burned stands [213]. Bunchberry importance was greater after fire than before fire in the first postfire growing season on fall-burned, spring-burned, and unburned plots in white pine and white pine-mixed hardwood stands in eastern New Hampshire. Increases were greatest in fall-burned plots and relatively small in spring-burned and unburned stands. Prescribed fires were low severity, "relatively cool, surface headfires". Average litter consumption for fall and spring fires was similar among stands: In burned mixed stands, 1.4 inches (3.5 cm) of litter was consumed and 1 inch (2.5 cm) remained; in burned white pine stands, 1 inch (2.5 cm) of litter was consumed and 0.6 inch (1.5 cm) remained [243].

Early postfire succession: The following studies present information on early postfire succession (primarily the first 10 postfire years). For longer postfire succession studies, see Fire-related forest succession.

Bunchberry is generally present in recently burned sites, but it may take several years to reach prefire or unburned abundance levels. Bunchberry appeared within 11 months of a wildfire in a balsam fir stand in northwestern Newfoundland, and within 10 years of the fire, formed an "almost complete carpet" in the understory layer. The wildfire lightly charred the surface layer [294]. Bunchberry frequency generally increased with each successive postfire sampling in the 3 years following a summer fire (1989) in black spruce/lichen and jack pine/lichen forests in northern Quebec's Ecomiak Lake area. In the 2nd postfire year, bunchberry frequency was evaluated multiple times over the growing season. Frequency was greatest in the last summer (August) sampling period [258].

Frequency (%) of bunchberry in the first 3 postfire growing seasons after a summer fire (1989) in northern Quebec [258]
Sampling date July 1990 June 1991 July 1991 August 1991 July 1992 July 1993
Black spruce/lichen 0.6 <0.5 <0.5 0.9 2.1 3.1
Jack pine/lichen 1.6 1.1 2.8 4.4 7.2 7.9

Cover of bunchberry typically peaked in the 2nd or 3rd postfire year after spring and summer fires in spruce-willow-birch vegetation in northern British Columbia and southern Yukon Territory. Cover and frequency declined in the 3rd or 4th postfire year, but bunchberry persisted as stands reached maturity [215]. Findings were similar when burned barrens vegetation in Newfoundland was evaluated 0.5 to 37 years after fire [220].

Frequency and cover of bunchberry on burned sites as time since fire increased in western Canada [220]
Time since fire (years) 0.5-1 2-5 6-9 10-19 20-36 37
Frequency (%) 64 92 67 71 86 70
Cover (%) 3 13 6 6 6 3

Effects of multiple fires: Two studies that evaluated twice-burned bunchberry habitats suggest that frequent fire may reduce bunchberry abundance. Bunchberry density and frequency were reduced 2 months after a June prescribed fire in a red and white pine stand at Ontario's Petawawa Forest Experimental Station. Bunchberry abundance was further reduced after a 2nd June fire the following year. Bunchberry density, frequency, and biomass remained below prefire levels 14 months after the 2nd fire. Prescribed fires were described as "gentle" and consumed all vegetation less than 12 inches (30 cm) tall. Fires burned into the litter but not into the duff. The 1st fire consumed 21% of the total available fuel and the 2nd fire consumed 5% of total available fuel. Fire intensities were similar, about 18 kcal/m/s [197]:

Density, frequency, and biomass of bunchberry before and after 1 and 2 fires in pine stands in Ontario [197]
Time since fire(s) Prefire 2 months after 1st fire 2 months after 2nd fire 14 months after 2nd fire
Density (stems/ha) 1,602 247 129 301
Frequency (%) 39 18 9 15
Biomass (kg/ha) 35.2 ----* ---- 3.9
* Not measured.

Bunchberry was more abundant in unburned quaking aspen stands than in stands burned twice in 5 years in central Alberta, while abundance was similar on unburned stands and stands burned only once in the same period. Bunchberry cover and frequency in the twice-burned stand were about 7% and 8% lower, respectively, than in unburned stands. The 1st prescribed fire occurred in fall 1972, produced an average depth of burn of 0.6 inch (1.5 cm) and a fireline intensity of 236 kW/m. The 2nd prescribed fire occurred in spring 1978, produced an average depth of burn of 1.4 inch (3.5 cm) and a fireline intensity of 4,392 kW/m, which is characteristic of a high-intensity surface fire [227]. See the Summary of this fire study by Quintilio and others for additional details.

Logged and burned sites: Bunchberry often persists after logging and burning [5,40,102] and may increase [102,117] unless the fire is severe [5,67]. Bunchberry occurred on cut and burned jack pine and black spruce stands in Manitoba and Saskatchewan that ranged from 2 to 5 years since the last disturbance [40,41,42]. In old-growth western hemlock-Sitka spruce forest in southeast Alaska, bunchberry cover was 5% greater on 7-year-old logged-and-burned than on logged-and-unburned sites. Winter logging removed saplings, pole-sized trees, snags, and left a moderate amount of slash. The "light" burn occurred in July after 6 days without rain [117]. Bunchberry density was about 70 stems/transect greater and cover was about 1% greater than predisturbance levels after clearcutting and 2 consecutive fires in a 25-year-old balsam fir-red pine woodlot in southwestern New Brunswick. Frequency of bunchberry, however, was about 7% lower than predisturbance levels on the cut and twice burned site [102]. In jack pine stands in Minnesota's Superior National Forest, bunchberry frequency increased on logged-and-burned sites when soil surface temperatures during slash burning were less than 900 °F (480 °C) but decreased when burning produced soil surface temperatures above 900 °F (480 °C). At the site of the cooler burn, the predisturbance frequency of bunchberry was 87%. In the first 3 postdisturbance years, bunchberry frequency was 90% to 100%. At the site of the hotter burn, the predisturbance frequency of bunchberry was 90%. In the 1st postdisturbance year, bunchberry frequency was 7%, and in the 2nd postdisturbance year was 63% [5]. Bunchberry was not present in the 1st or 2nd years after clearcutting and fire in the floodplain white spruce forest type on Willow Island near Fairbanks, Alaska. Prior to the disturbances, bunchberry cover was 5.7% and frequency was 90%. The fire was considered severe; researchers reported ash and mineral soil but no charred material on the burned site [67].

On logged-and-burned sites, it is common for bunchberry abundance to increase as time since disturbance increases. However, the length of time for increases varies. In clearcut and slash-burned old-growth Douglas-fir forest in Oregon's HJ Andrews Experimental Forest, frequency of bunchberry generally increased rapidly in the first 4 to 5 postfire years but increased more slowly thereafter [314]. On northern Vancouver Island, the above- and belowground bunchberry biomass increased as time since fire increased from 2 to 8 years in clearcut-and-burned areas. Aboveground bunchberry biomass averaged 2 lbs (1 kg)/ha on 2-year-old, 57 lbs (26 kg)/ha on 4-year-old, and 895 lbs (406 kg)/ha on 8-year-old clearcut-and-burned plots. Biomass was significantly greater on 8-year-old than 2- or 4-year-old sites (P<0.05). Fine root biomass and small rhizome biomass increases were large between the 4th and 8th postdisturbance years [195].

Cover of bunchberry exceeded prefire levels 3 to 5 years after clearcutting and burning in subalpine fir and western white spruce (Engelmann spruce × white spruce) forest sites in British Columbia. Sites were clearcut in the winter and burned the following summer. Bunchberry cover increased with time since disturbance up to the 5th or 10th postfire year [108,109]:

Average cover (%) of bunchberry after fire in clearcut forest sites in British Columbia [108]
Site as described by burn characteristics Time since disturbance (years)

Before fire,
after clearcutting

1 2 3 5 10
Fairly low severity; 28.5% woody fuel consumption; average depth of burn: 1 cm [108] 8.00 3.0 7.5 10.2 11.7 2.2
Moderate severity; 47.7% woody fuel consumption; average depth of burn: 3.8 cm [109] 10.0 2.2 4.3 8.0 12.5 15.0
Moderate severity; 58.6% woody fuel consumption; average depth of burn: 1.8 cm [109] present
(no cover data)
1.5 2.2 3.0 4.8 6.2

Comparing canopy-removal disturbances: When studies compared burned, logged, and logged-and-burned sites, there were no clear trends in bunchberry abundance. Three studies reported greater bunchberry cover on burned than logged or logged-and-burned sites [101,139,146], and 3 reported lower bunchberry cover on burned than logged or logged-and-burned sites [106,135,216]. In another study, bunchberry cover was greater on burned (21%) than logged-and-burned (17%) stands about 4 years after disturbance in jack pine-black spruce stands in the Superior National Forest in Minnesota; and greater on logged-and-burned (9%) than burned (2%) stands about 14 years after disturbance in jack pine-black spruce stands in Quetico Provincial Park, Ontario [211].

Bunchberry was significantly (P<0.05) more abundant in burned than clearcut quaking aspen stands in the southern boreal region of Ontario. Researchers determined that prior to the disturbances physiographic, soil, and stand characteristics were not significantly different between burned and clearcut stands at the site, stand, or landscape scales. Sites were visited 3 years after disturbances. Logging occurred in summer or winter of 1996 or 1997, and wildfires burned as crown fires in late May or early June 1997 [101].

Cover of bunchberry was greater on burned than logged stands in boreal mixedwoods in southeastern Manitoba but was greatest in stands impacted by spruce budworm. Sites were disturbed 10 to 15 years prior to the study. Bunchberry cover averaged 6.3% in stands severely impacted by spruce budworm, 2.9% in burned stands, and 1.1% in logged stands. Researchers thought that gradual increases in light by canopy removal from budworm may have promoted increases in established understory species, whereas rapid increases in light from immediate canopy removal may have favored increases and establishment of fast-growing, shade-intolerant species [139].

In midboreal mixedwood stands burned by wildfire in Alberta, bunchberry cover was significantly (P≤0.03) greater on sites that were not salvage logged than on sites that were salvage logged. In early postdisturbance succession, density of deciduous saplings was greater and litter cover and downed wood were less on burned than burned-and-logged sites. In mid-seral stands, organic matter depths and soil moisture were greater and woody stem densities were less on burned than burned-and-logged sites [146].

Average cover and frequency of bunchberry on burned and burned-and-salvage logged sites 2 and 34 years after a wildfire in midboreal mixedwood stands in Alberta [146]
  Burned Burned and logged
Early-seral stands (2 years since fire)
Cover (%) 6.7 3.6
Frequency (%) 100 93
Mid-seral stands (34 years since fire)
Cover (%) 5.7 3.5
Frequency (%) 100 85

Bunchberry cover was much lower before than 2 to 11 years after prescribed fire in a clearcut Engelmann spruce-subalpine fir stand in interior British Columbia. The fire was considered severe. Average total woody fuel consumption was 53%, and the average depth of burn was 1.2 inches (3.1 cm). Stands were clearcut in winter 1987-88, vegetation was measured in the 1988 growing season, and the prescribed fire burned in mid-September 1989. Bunchberry cover averaged 6.1% before the fire in the clearcut area, and 11%, 20.5%, and 27.9% in the 2nd, 5th, and 11th postfire years, respectively [106]. Findings were similar 2 to 10 years after slash burning in a clearcut area in the very wet and cool zone of the sub-boreal forest in northern British Columbia. Bunchberry cover was less than 1% after winter clearcutting operations, but 5 years after slash burning, bunchberry cover increased to 5.4% and 8.2% in logged areas where the forest floor remained intact and on skid roads where mineral soil was exposed, respectively. Slash burning occurred in mid-August following clearcutting in the previous winter. Average woody fuel consumption was 32%. Average forest floor consumption was 17%, and the average depth of burn was about 0.8 inch (2 cm) [107]. For additional details on these studies, see the original research papers by Hamilton (2006a and 2006b).

Relative bunchberry cover was greatest on clearcut sites when researchers compared undisturbed, clearcut, burned, and clearcut-and-burned black spruce stands in northwestern Ontario. Relative cover of bunchberry was less than 1% in 60- to 70-year-old, undisturbed forest, 1% in wildfire-burned forest, and 13% in clearcut forest. Bunchberry was absent from clearcut-and-burned stands. Surface fuel was more abundant and the wildfire much more intense in the clearcut (71,000 kW/m calculated) than in uncut stands (21,000 kW/m). The wildfire burned on 12 June when the temperature was 88 °F (31 °C), relative humidity was 52%, and wind speeds were 11 km/h [135]. Bunchberry density was highest on winter-logged sites when control, spring-logged, winter-logged, and winter-logged-and-burned sites were compared in the spruce-fir zone at the University of Minnesota's Cloquet Forestry Center. Density of bunchberry in the 1st and 2nd years after spring logging and in the 1st year after burning the winter-logged site was significantly (P<0.05) lower than bunchberry density on control and winter-logged sites [216].

No differences in bunchberry frequency were found between undisturbed, clearcut, and burned portions of black spruce forest in central Quebec, but bunchberry frequency increased with time since disturbance in burned-and-logged stands. Frequency of bunchberry was about 60% less in areas burned 2 years earlier than in areas burned 14 years earlier and in areas logged 5 years earlier than in areas logged 16 years earlier [209].

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  • 215. Oswald, E. T.; Brown, B. N. 1990. Vegetation establishment during 5 years following wildfire in northern British Columbia and southern Yukon Territory. Information Report BC-X-320. Victoria, BC: Forestry Canada, Pacific and Yukon Region, Pacific Forestry Centre. 46 p. [16934]
  • 216. Outcalt, Kenneth Wayne; White, Edwin H. 1981. Phytosociological changes in understory vegetation following timber harvest in northern Minnesota. Canadian Journal of Forest Research. 11(1): 175-183. [16301]
  • 219. Peltzer, Duane A.; Bast, Marcy L.; Wilson, Scott D.; Gerry, Ann K. 2000. Plant diversity and tree responses following contrasting disturbances in boreal forest. Forest Ecology and Management. 127(1-3): 191-203. [48541]
  • 220. Peters, Stuart S. 1958. The ecological effects of fire and its possible application to game management. In: Proceedings, symposium on prescribed burning in forestry, agriculture, and wildlife management. Newfoundland Research Committee Publication No. 1. St. John's, Newfoundland: Memorial University of Newfoundland, Department of Mines and Resources: 41-52. [36589]
  • 225. Purdon, Mark; Brais, Suzanne; Bergeron, Yves. 2004. Initial response of understory vegetation to fire severity and salvage-logging in the southern boreal forest of Quebec. Applied Vegetation Science. 7(1): 49-60. [3412]
  • 227. Quintilio, D.; Alexander, M. E.; Ponto, R. L. 1991. Spring fires in a semimature trembling aspen stand in central Alberta. Information Report NOR-X-323. Edmonton, AB: Forestry Canada, Northwest Region, Northern Forestry Centre. 30 p. [19243]
  • 243. Ross, S. Rachel. 1978. The effects of prescribed burning on ground cover vegetation of white pine and mixed hardwood forests in southeastern New Hampshire. Durham, NH: University of New Hampshire. 151 p. Thesis. [20674]
  • 258. Sirois, Luc. 1995. Initial phase of postfire forest regeneration in two lichen woodlands of northern Quebec. Ecoscience. 2(2): 177-183. [27068]
  • 259. Skutch, Alexander F. 1929. Early stages of plant succession following forest fires. Ecology. 10(2): 177-190. [21349]
  • 267. Stephenson, David E. 1985. The use of charred black spruce bark by snowshoe hare. The Journal of Wildlife Management. 49(2): 296-300. [8451]
  • 280. Swain, Albert M. 1973. A history of fire and vegetation in northeastern Minnesota as recorded in lake sediments. Quaternary Research. 3(3): 383-396. [38931]
  • 294. Van Nostrand, R. S. 1965. Results of experimental seeding of balsam fir on a recent burn. Department of Forestry Publication No. 1103. Ottawa, ON: Canadian Department of Forestry, Research Branch. 10 p. [41914]
  • 314. Yerkes, Vern P. 1960. Occurrence of shrubs and herbaceous vegetation after clear cutting old-growth Douglas-fir. Res. Pap. PNW-34. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station. 12 p. [8937]
  • 301. Wang, G. Geoff; Kemball, Kevin J. 2003. The effect of fire severity on early development of understory vegetation following a stand replacing wildfire--3B.2, [Online]. In: Proceedings, 2nd international wildland fire ecology and fire management congress held concurrently with the 5th symposium on fire and forest meteorology; 2003 November 16-20; Orlando, FL. Boston, MA: American Meteorology Society (Producer): Available: http://ams.confex.com/ams/FIRE2003/techprogram/paper_65430.htm [2006, October 27]. [64194]

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Post-fire Regeneration

More info for the terms: rhizome, secondary colonizer

Postfire regeneration strategy
[270]:
Rhizomatous herb, rhizome in soil
Secondary colonizer (on- or off-site seed sources)
  • 270. Stickney, Peter F. 1989. Seral origin of species comprising secondary plant succession in Northern Rocky Mountain forests. FEIS workshop: Postfire regeneration. Unpublished draft on file at: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory, Missoula, MT. 10 p. [20090]

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Immediate Effect of Fire

More info for the terms: cover, duff, resistance, rhizome

Bunchberry is typically only top-killed by fire; postfire sprouting is common [37,173]. Rhizomes typically reach the mineral soil layer and are covered by about 1.6 to 5 inches (4-13 cm) of duff or soil [78,191]. With reproductive organs at these depths, bunchberry is considered intermediate in fire damage resistance among ground cover species in British Columbia's Douglas-fir forest zone. It is generally expected to survive fires that fail to raise soil temperatures appreciably or produce long-term soil heating [191]. Bunchberry rhizomes are sensitive to heating [77,169] (see Rhizome characteristics). Therefore, on sites where rhizome depths do not penetrate beyond the duff layer or the top few centimeters of mineral soil (e.g., [78]), bunchberry may not survive fires that consume the entire duff layer.
  • 78. Flinn, Marguerite A.; Wein, Ross W. 1977. Depth of underground plant organs and theoretical survival during fire. Canadian Journal of Botany. 55(19): 2550-2554. [6362]
  • 169. Long-Robinson, Tammy M. 1990. A study of the clonal behavior of Cornus canadensis. Biology 556, Boreal Flora. Pellston, MI: University of Michigan, Biological Station. 18 p. [83948]
  • 173. Lynham, T. J.; Curran, T. R. 1998. Vegetation recovery after wildfire in old-growth red and white pine. Frontline: Forestry Research Applications/Technical Note No. 100. Sault Ste. Marie, ON: Natural Resources Canada, Canadian Forest Service, Great Lakes Forestry Centre. 4 p. [30685]
  • 191. McLean, Alastair. 1968. Fire resistance of forest species as influenced by root systems. Journal of Range Management. 22(2): 120-122. [1621]
  • 77. Flinn, Marguerite A.; Pringle, Joan K. 1983. Heat tolerance of rhizomes of several understory species. Canadian Journal of Botany. 61(2): 452-457. [8444]
  • 37. Chapman, Rachel Ross; Crow, Garrett E. 1981. Application of Raunkiaer's life form system to plant species survival after fire. Bulletin of the Torrey Botanical Club. 108(4): 472-478. [617]

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Successional Status

More info on this topic.

More info for the terms: bog, climax, cover, eruption, frequency, hardwood, phase, restoration, severity, shrubs, stand-replacing fire, succession, tree

Bunchberry tolerates the range of conditions present from early to late forest succession [57,103,104,241]. Bunchberry abundance can be greater in open-canopy than closed-canopy habitats, but it still persists in dense forest shade. If the canopy is removed but soil is left intact, bunchberry "exists indefinitely" as the new canopy develops [103]. Bunchberry cover can be similar in young and mature forests, but it is more commonly described as a dominant understory species in mature than young forests. This may reflect the rarity of other understory species in mature or old-growth stands rather than an abundance of bunchberry.

Shade relationships: Bunchberry grows in habitats ranging from full sun to nearly complete shade [145,151,177,303]. Studies report each of the following conditions: greater abundance of bunchberry in closed-canopy than open-canopy sites [16,19,51], greater abundance of bunchberry in open-canopy than closed-canopy sites [8,59,277], and similar abundance in open-canopy and closed-canopy sites [208,224,269]. There was no discernable pattern to bunchberry's abundance as related to light availability, but large, open sites devoid of grasses and shrubs that could shade a low-growing species such as bunchberry were rarely described.

The following studies reported that the abundance of bunchberry was greatest in sites with low light conditions. In western white pine stands in northern Idaho, bunchberry was restricted to shady sites that occurred beneath tree canopies and "disappear(ed)" after clearcutting [157,158]. Cover of bunchberry was greater in mature (120-year old) lodgepole pine stands than in stands clearcut 6 to 12 years earlier in the Lower Foothills of Alberta [51]. In west-central Alberta, bunchberry cover increased as forest canopy cover increased. Average cover was significantly lower in early-seral (2.5%) than mid-seral (7.6%) stands (P<0.001); forest canopy was less than 30% in early-seral stands and greater than 30% in mid-seral stands [16]. In the Chippewa National Forest in north-central Minnesota, the greatest frequency of bunchberry occurred in red pine forest plots receiving less than 20% of full light [255]. When overstory and understory patterns were studied over a large area of northwestern Quebec, which included quaking aspen, mixed deciduous-conifer forests, and old-growth northern whitecedar forests, researchers found that bunchberry was associated with low light levels and conifer canopies [19].

Bunchberry abundance was greater in open-canopy than closed-canopy forests in many studies. Bunchberry flower and seed crops were "heavy" on logging roads scraped of vegetation [263]. In the Chugach National Forest on the Kenai Peninsula of Alaska, bunchberry cover increased as overstory canopy cover reached 50% then decreased as canopy cover reached 100% [277]. In Sitka spruce-western hemlock forests in southeastern Alaska, bunchberry cover was significantly less (P<0.01) beneath the canopy than in canopy gaps [8]. Bunchberry biomass was significantly greater (P=0.03) in boreal mixedwood forest plots where all erect shrubs were removed than in plots where shrubs were retained. The amount of diffuse, direct, and total incoming light at 20 inches (50 cm) above ground was significantly lower in control than removal plots (P<0.0017) [38]. In early-seral, shrub-dominated communities regenerating after logging and/or fire in the western redcedar-western hemlock zone in northern Idaho, frequency of bunchberry was greatest in stands with 26% to 55% tree canopy cover and least on sites with 56% to 100% canopy cover [202]. In southern boreal forests along Lake Duparquet in northwestern Quebec, bunchberry cover was typically greater after experimental canopy gaps were created. Bunchberry abundance was compared before and up to 4 years after gap creation [59]. In red spruce forests near Liverpool, Nova Scotia, abundance of bunchberry was high in semi-open clearcut forests and in mature forests with large canopy gaps [199]. Bunchberry was considered "prolific" in full sun to partial shade mixedwood forests but also occurred in spruce and fir forests with dense shade in the Adirondack Uplands of New York [145].

In several other studies there was little to no difference in bunchberry abundance related to degree of shading. Cover and frequency of bunchberry were nearly identical in harvested and canopy tree retention sites in a mixed-conifer forest on the west slope of the Cascade Range in southwestern Washington. Percentage of open sky was 17% in retention and 45% in harvest areas. Cover of logging slash was 10% in retention and 66% in harvest areas [208]. In the Willamette National Forest, Oregon, bunchberry cover was 20.6% beneath Douglas-fir canopies and 26.9% in canopy openings [269]. Cover of bunchberry was not significantly different in a tornado blow down area and an adjacent undisturbed site in mixed-conifer-northern hardwood forests in the Boundary Waters Canoe Wilderness Area. Researchers evaluated the sites 1, 2, 3, and 4 years following the tornado [224].

Disturbance tolerance: Bunchberry is rarely killed by forest disturbances, but abundance of bunchberry is often lower on disturbed than undisturbed sites, which may relate to the disturbance itself or changes in the mircoenvironment resulting from the disturbance. In the Harvard Forest in Petersham, Massachusetts, bunchberry frequency (8%) had not recovered to pre-hurricane levels (18%) within 53 years of a hurricane [175]. In mixed-conifer forests impacted by the eruption of Mount St Helens, bunchberry frequency was greater in scorched areas (33%), where trees were killed but remained standing, than in blow down areas (15%), where trees were killed and snapped or uprooted [193]. Bunchberry was associated with the least disturbed sites when restoration sites and naturally recovering sites were compared in the industrially impacted area of Sudbury, Ontario. Forests were damaged by logging, mining, and smelting operations that began in the 1800s [229].

Abundance of bunchberry can be reduced by logging. Bunchberry cover was negatively correlated (r = -0.650) with mechanical site treatments, when cleared and mechanically treated boreal and sub-boreal sites were visited 10 years after logging. Severity of the treatments ranged from low to high severity and included disk trenching, plowing, rotoclearing, and/or windrow burning [100]. In the Cascade Range in Oregon and Washington, bunchberry occurred in young, mature, and old-growth Douglas-fir forests. However, its development was best in old-growth stands, and it was considered sensitive to disturbance based on the evaluation of experimental stands that were logged, clearcut, and/or slash burned [104]. When disturbed and undisturbed western redcedar-western hemlock stands were compared in northern Idaho, average bunchberry cover was greatest (12%) in 100-year-old, undisturbed stands. Average bunchberry cover was much lower (<1-4%) in stands clearcut, thinned, or burned 30 years earlier [131]. Bunchberry cover decreased on both undisturbed and clearcut plots in a mixed coniferous-deciduous forest in southeastern New Brunswick. Average cover of bunchberry had decreased by about 1% on the undisturbed and clearcut sites when evaluated in the second posttreatment year. On a site that was clearcut, scarified, and planted with the jack pine seedlings, average bunchberry cover increased 0.4% from pretreatment levels [237].

Bunchberry is likely to persist following disturbance. Cover of bunchberry was similar in unlogged and salvage logged portions of a severely wind-damaged black spruce-jack pine forest in Minnesota's Superior National Forest. Two years after the microburst and 1 year after salvage logging, bunchberry cover was 5.2% in unlogged and 6.5% in salvage-logged areas. A year later, bunchberry cover was 1.3% in unlogged and 3.2% in salvage-logged areas [152]. On caribou summer range in northern Quebec and Labrador, bunchberry cover was not significantly different between grazed (1.8%) and ungrazed (1.0%) areas [180].

Forest succession: Generally bunchberry can occur in all stages of forest succession. Bunchberry occurred in nearly all of 121 plots surveyed throughout the entire range of black spruce in British Columbia. Forest age ranged from 37 to about 185 years old and included a wide range of soil moisture, nutrient, and aeration conditions [142]. Two successional trends were identified in the boreal forest zone of west-central Alberta, and bunchberry occurred in nearly all successional forest types, including communities transitioning from lodgepole pine and quaking aspen to white spruce on moist, low-elevation uplands, and communities transitioning from lodgepole pine and black spruce to spruce-subalpine fir forests on moist but well-drained, high-elevation uplands [49]. In Montana's Glacier National Park, bunchberry was more frequent in pioneer and early-seral lodgepole pine forests than in late-seral and climax western hemlock and western redcedar forests [98], but it was considered common in climax western redcedar and grand fir (Abies grandis) stands over 300 years old in Idaho's Selway-Bitterroot Wilderness [99]. In Isle Royale National Park, bunchberry occurs in the early succession of rocky sites [44] and in climax balsam fir-paper birch-white spruce forests [45]. In a region south of James Bay in Ontario and Quebec, researchers surveyed 197 boreal forest stands and found bunchberry throughout the studied stand types. Abundance of bunchberry was similar along the full spectrum of successional stages identified [35].

In forested wetland or riparian sites, bunchberry may be restricted to later seral stages. Along the Chena River near Fairbanks, Alaska, bunchberry occurred in older floodplain terraces and upper elevations. Bunchberry did not occur in 15-year-old willow (Salix spp.) or 50-year-old balsam poplar (Populus balsamifera) stands, but did occur in 120-year-old white spruce, 220-year-old white spruce-black spruce, and climax black spruce/sphagnum (Sphagnum spp.) stands. Soil froze quicker, deeper, and reached lower temperatures in the early-seral deciduous stands than in late-seral conifer stands [296]. Xerosere and hydrosere successions occur in Algonquin Park, Ontario, where the climatic climax species is eastern hemlock. Xerosere succession involves transitioning from pioneer woodlands dominated by red maple, quaking aspen, paper birch, or jack pine to white pine or balsam fir-white spruce forests, then to eastern hemlock forest. Bunchberry occurs in nearly all forest types along the xerosere. In hydrosere succession, which involves transitioning from bog vegetation to black spruce and balsam fir forests and then to eastern hemlock forest, bunchberry is restricted to later successional stages [185].

Fire-related forest succession: Generally bunchberry can be present in recently burned as well as long unburned forests throughout its range. Studies suggest, however, that bunchberry abundance is lower in early postfire succession than later successional stages.

Bunchberry typically survives fire. Bunchberry frequency was relatively consistent in fire-origin lodgepole pine stands less than 100 years old in Banff and Jasper National Parks in Alberta [149]. In southeastern Manitoba, bunchberry occurred in severely burned 5-year-old stands and forests over 90 years old [247]. In northern Lower Michigan, bunchberry was described as a relic species. It occurred in mature pine, fir, and spruce stands, and after fire, it occurred in early-seral quaking aspen forests colonizing the burned area [92]. On Isle Royale, bunchberry "thrive(s) better than ever after the destruction of forest cover" by fires consuming only small amounts of the humus layer [46]. Bunchberry occurred on all burned sites in the boreal region of northwestern Ontario that experienced "intense, fast-spreading" wildfires 1, 4, 14, and 45 years earlier [196]. In coniferous and mixedwood forests of southwestern Nova Scotia, bunchberry was present in nearly all 1- to 40-year-old burned stands [183]. See the section on Early postfire succession for more information.

Bunchberry can occur on burned sites 1 to 400+ years old, but abundance of bunchberry is often lower in the early than the mid- or late stages of forest regeneration. In central Alaska, bunchberry was considered a late-seral dominant in burned white spruce forests. Researchers surveyed stands from the initiation phase (1-5 years since fire) through the mature hardwood phase (75-95 years since fire) [231]. In the spruce region of interior British Columbia, bunchberry's frequency index was 8 in stands burned 4 to 22 years prior and 10 in stands burned 37 to 75 years prior. A value of 10 indicated the most uniform distribution [91]. In black spruce forests in northern Saskatchewan, bunchberry was a dominant in stands burned 11 to more than 30 years prior but not in stands burned less than 10 years prior [253]. In black spruce or jack pine boreal forest stands in northern Quebec, bunchberry was more common on sites burned 16 to 110 years prior than sites burned less than 10 years prior [81]. In sub-boreal forests of west-central British Columbia, bunchberry had the highest cover of all herbaceous forest species in all but the youngest stands, although the absolute cover of bunchberry was greatest in these young stands. Early-seral forests were dominated by lodgepole pine, which rarely lived beyond 200 years. Subalpine fir and Engelmann spruce established in young stands and increased in abundance as forests aged [43].

Average cover of bunchberry along a postfire chronosequence in sub-boreal British Columbia [43]
Forest age (yrs) 0-50 51-100 101-150 151-200 201-250 251-300 301-350 351-400 400+
Bunchberry cover (%) 11.0 4.5 6.9 10.0 3.8 1.5 4.5 3.3 7.3

Although it is common to find more bunchberry in the mid- and late stages than in the early stages of a postfire chronosequence, there are exceptions to this trend. Along a postfire chronosequence spanning 80 years in burned jack pine-black spruce forests in northeastern Minnesota, cover was lowest (5%) in 1-year-old burned plots, ranged from 9% to 12% in 2- to 5-year-old burned plots, 12% to 16% in 10- to 20-year-old burned plots, and 8% to 10% in 30- to 80-year old burned plots [3]. In northeastern New Brunswick, there were no consistent differences in bunchberry abundance with time since fire in jack pine and black spruce stands [176]. Bunchberry was most abundant in 2-year-old and 140-year-old forest plots in open black spruce stands in western Labrador, compared to 18-, 40-, and 80-year-old stands [257]. In southeastern Labrador, the frequency of bunchberry was 100% in paper birch stands burned 6 to 100 years prior. Frequency of bunchberry ranged from 40% to 95% in black spruce or balsam forests unburned for more than 100 years [82].

Bunchberry often dominated 50- to 200-year-old stands when long postfire chronosequences were evaluated. In white spruce forests in central Alaska, bunchberry and field horsetail (Equisetum arvense) typically replaced bluejoint reedgrass (Calamagrostis canadensis) and fireweed (Chamerion angustifolium) as the dominant understory species in hardwood stands 51 to 100 years after fire. Bunchberry persists 100 to 250 years after fire in white spruce-hardwood and mature white spruce/moss stands. The changes occurring once forests age beyond 200 years are relatively unknown because white spruce forests of that age are rare in Alaska's interior [292]. In Isle Royale National Park, the relative cover of bunchberry was greater in older stands that developed after stand-replacing fire. Bunchberry was unimportant in 40- and 99-year old stands. Relative cover was 4.3%, 8.9%, and 8.3% in 117-year-old, 170-year-old, and 223-year-old stands, respectively. As stand age increased, the relative densities of balsam fir and white spruce increased and paper birch and quaking aspen decreased [132]. Bunchberry cover was greatest, although still low, in 167- and 174-year-old stands in a chronosequence spanning 26 to 230 years since stand-replacing fire in southern boreal forests along Lake Duparquet in northwestern Quebec [60].

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  • 180. Manseau, M.; Huot, J.; Crete, M. 1996. Effects of summer grazing by caribou on composition and productivity of vegetation: community and landscape level. Journal of Ecology. 84(4): 503-513. [26980]
  • 183. Martin, J. Lynton. 1956. An ecological survey of burned-over forest land in southwestern Nova Scotia. The Forestry Chronicle. 32(3): 313-336. [8932]
  • 185. Martin, N. D. 1959. An analysis of forest succession in Algonquin Park, Ontario. Ecological Monographs. 29(3): 187-218. [19930]
  • 193. Means, Joseph E.; McKee, W. Arthur; Moir, William H.; Franklin, Jerry F. 1982. Natural revegetation of the northeastern portion of the devastated area. In: Keller, S. A, C.; ed. Mount St. Helens: one year later: Proceedings of a symposium; 1981 May 17-18; Cheney, WA. Cheney, WA: Eastern Washington University Press: 93-103. [5977]
  • 196. Methven, I. R.; Van Wagner, C. E.; Stocks, B. J. 1975. The vegetation of four burned areas in northwestern Ontario. Inf. Rep. PS-X-60. Chalk River, ON: Canadian Forestry Service, Petawawa Forest Experiment Station. 10 p. [13114]
  • 199. Moola, F. M.; Vasseur, L. 2004. Recovery of late-seral vascular plants in a chronosequence of post-clearcut forest stands in coastal Nova Scotia, Canada. Plant Ecology. 172(2): 183-197. [83930]
  • 208. Nelson, Cara R.; Halpern, Charles B. 2005. Edge-related responses of understory plants to aggregated retention harvest in the Pacific Northwest. Ecological Applications. 15(1): 196-209. [61474]
  • 224. Powell, Roger A.; Brooks, William S. 1981. Small mammal changes in populations following tornado blowdown in northern mixed forest. Journal of Mammalogy. 62(2): 397-400. [61244]
  • 229. Rayfield, Bronwyn; Anand, Madhur; Laurence, Sophie. 2005. Assessing simple versus complex restoration strategies for industrially disturbed forests. Restoration Ecology. 13(4): 639-650. [60346]
  • 237. Roberts, Mark R.; Zhu, Lixiang. 2002. Early response of the herbaceous layer to harvesting in a mixed coniferous-deciduous forest in New Brunswick, Canada. Forest Ecology and Management. 155(1-3): 17-31. [40747]
  • 247. Schaefer, James A. 1993. Spatial patterns in taiga plant communities following fire. Canadian Journal of Botany. 71(12): 1568-1573. [25527]
  • 253. Scotter, George Wilby. 1964. Effects of forest fires on the winter range of barren-ground caribou in northern Saskatchewan. Wildlife Management Bulletin. Series 1. No. 18. Ottawa, ON: Canadian Wildlife Service, National Parks Branch, Department of Northern Affairs and National Resources. 111 p. [28989]
  • 255. Shirley, Hardy L. 1932. Light intensity in relation to plant growth in a virgin Norway pine forest. Journal of Agricultural Research. 44: 227-244. [10360]
  • 269. Stewart, G. H. 1988. The influence of canopy cover on understory development in forests of the western Cascade Range, Oregon, USA. Vegetatio. 76: 79-88. [6631]
  • 277. Suring, Lowell H.; Goldstein, Michael I.; Howell, Susan M.; Nations, Christopher S. 2008. Response of the cover of berry-producing species to ecological factors on the Kenai Peninsula, Alaska, USA. Canadian Journal of Forest Research. 38(5): 1244-1259. [83935]
  • 296. Viereck, Leslie A. 1970. Forest succession and soil development adjacent to the Chena River in interior Alaska. Arctic and Alpine Research. 2(1): 1-26. [12466]
  • 303. Waterman, W. G. 1922. Development of plant communities of a sand ridge region in Michigan. Botanical Gazette. 74(1): 1-31. [63565]
  • 131. Irwin, Larry L. 1976. Effects of intensive silviculture on big game forage sources in northern Idaho. In: Hieb, S., ed. Proceedings, elk-logging roads symposium; [1975 December 16-17]; [Moscow, ID]. Moscow, ID: University of Idaho: 135-142. [16146]

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Vegetative regeneration

More info for the terms: density, eruption, rhizome, swamp

Bunchberry clones can be extensive, but the size of clones and abundance of nodes and sprouts along rhizomes vary by site and are likely greater in high-light environments. Three large bunchberry clones were excavated as completely as possible from a stream bank near Reese's Swamp in Cheboygan County, Michigan. The greatest total length of rhizomes for an individual clone was 13.8 feet (4.2 m), and the greatest depth from which rhizomes were recovered was 11.8 inches (30 cm) [169]. Bunchberry rhizome length, annual growth, and number of nodes were greater in clearcut stands than in young and old-growth stands in southeastern Alaska. Old-growth stands were dominated by western hemlock and Sitka spruce; young stands were clearcut 40 years earlier, and clearcut stands were 4- to 6-years old. The longest living bunchberry rhizome found was 172 inches (436 cm) and was estimated to be 36 years old. The longest internode length found was 30 inches (75 cm) and occurred in an area where the rhizome grew through decayed logs [282]. Bunchberry rhizomes are also described in Belowground description.

Average characteristics of bunchberry clones in old-growth, young, and clearcut stands in the western hemlock-Sitka spruce zone in southeastern Alaska [282]
Stand type* Old-growth Young Clearcut
Total rhizome length (cm) 165 15 309
Annual rhizome growth (cm) 9 4 131
Nodes/clone (number) 9 not measured 20
*Percentage of open canopy: old-growth 2.8-6.4%; young 0.6-2.3%; clearcut 100%.

Bunchberry rhizomes may sprout when light availability increases [14] or aboveground stems are buried [12] or killed (see Plant response to fire). After the eruption of Mount St Helens, bunchberry stems grew through 3.5 inches (9 cm) of ash [12]. In Oneida County, Wisconsin, density of bunchberry stems increased from 30 to 94 shoots/m² within a year after canopy removal [14].

Research suggests that bunchberry's dispersal potential from rhizome pieces may be limited. In southeastern Canada, 3-foot (1 m) long sections of bunchberry rhizomes were dug from forest sites and transplanted within an hour into a common garden. Rhizome sections were planted at a depth equal to that from which they were excavated at the forest sites. Five months after transplanting, bunchberry regrowth was poor from transplanted rhizomes [79].

  • 14. Armentano, Thomas Vincent. 1973. Population ecology and response to stress of Aster macrophyllus and Cornus canadensis. Chapel Hill, NC: University of North Carolina at Chapel Hill. 211 p. Dissertation. [83945]
  • 169. Long-Robinson, Tammy M. 1990. A study of the clonal behavior of Cornus canadensis. Biology 556, Boreal Flora. Pellston, MI: University of Michigan, Biological Station. 18 p. [83948]
  • 12. Antos, Joseph A.; Zobel, Donald B. 1985. Plant form, developmental plasticity and survival following burial by volcanic tephra. Canadian Journal of Botany. 63(12): 2083-2090. [12553]
  • 79. Flinn, Marguerite Adele. 1980. Heat penetration and early postfire regeneration of some understory species in the Acadian forest. Halifax, NB: University of New Brunswick. 87 p. Thesis. [9876]
  • 282. Tappeiner, J. C.; Alaback, P. B. 1989. Early establishment and vegetative growth of understory species in the western hemlock-Sitka spruce forests of southeast Alaska. Canadian Journal of Botany. 67(2): 318-326. [8931]

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Germination

More info for the terms: duff, litter

Bunchberry seed germinates best when a cold stratification period is followed by alternating temperatures [63] and light [282].

Several controlled studies report that bunchberry seed fails to germinate without cold stratification [2,190,210]. Maximum germination of bunchberry seed collected from Kamloops, British Columbia, was 38% after stratification [190]. Maximum germination was 2% when bunchberry seed was not exposed to cold temperatures or was dried before cold temperature exposure. When seeds overwintered outdoors, germination was 28% [2]. Bunchberry seeds collected in August from the Bonanza Creek Experimental Forest in central Alaska germinated best when cold stratified and subsequently exposed to alternating cool and warm temperatures 43 to 81 °F (6-27 °C). Germination was significantly less (P<0.05) for cold stratified seeds exposed to constant temperatures and for seeds exposed to warm and cold pretreatments before exposure to either constant or alternating germination temperatures [63].

Field and laboratory studies indicate that bunchberry germination typically occurs in the spring and is best for unburied seed. In central Alaska, germination of bunchberry seed was much better for uncovered than buried seeds. Most seed germinated in June, and all seed germinated by the end of July. Seeds sown in late August did not germinate in the fall [63]. For bunchberry seed collected near Juneau, Alaska, germination in the laboratory was 61% to 87% after cold stratification. In the field, the average germination of uncovered seed was 78%. Seeds buried by 0.4 inch (1 cm) of litter and/or duff material germinated poorly (1-8%). Bunchberry seedlings emerged over a 3-year period for 2 seeding trials [282]. See Seed banking for details.

Bunchberry seedling emergence is possible on sunny, shady, burned, or unburned sites. Emergence of bunchberry was greater in old-growth (22%) than in young (12%) western hemlock-Sitka spruce stands near Juneau, Alaska. The percentage of light and canopy openings was greater in old-growth than young stands [282]. When seedling emergence was evaluated in the greenhouse in soil samples that were experimentally exposed to shady, sunny, disturbed, undisturbed, burned, and unburned conditions, bunchberry emergence was low but did not appear sensitive to any one condition. Two bunchberry seedlings emerged from a 1,560 cm³ soil sample that was collected and kept as an undisturbed block of forest soil, put under shade cloth, and burned with a propane torch. Two seedlings also emerged from a soil block that was thoroughly mixed, exposed to full sun, and not burned. Soil blocks were collected in late April from old-growth Douglas-fir stands in Oregon's HJ Andrews Experimental Forest [130].

  • 2. Adams, John. 1927. The germination of the seeds of some plants with fleshy fruits. American Journal of Botany. 14(8): 415-428. [48174]
  • 63. Densmore, Roseann Van Essen. 1979. Aspects of the seed ecology of woody plants of the Alaskan taiga and tundra. Durham, NC: Duke University. 285 p. Dissertation. [70495]
  • 130. Ingersoll, Cheryl A.; Wilson, Mark V. 1990. Buried propagules in an old-growth forest and their response to experimental disturbances. Canadian Journal of Botany. 68(5): 1156-1162. [11767]
  • 190. McLean, Alastair. 1967. Germination of forest range species from southern British Columbia. Journal of Range Management. 6(5): 321-322. [83928]
  • 210. Nichols, G. E. 1934. The influence of exposure to winter temperatures upon seed germination in various native American plants. Ecology. 15(4): 364-373. [55167]
  • 282. Tappeiner, J. C.; Alaback, P. B. 1989. Early establishment and vegetative growth of understory species in the western hemlock-Sitka spruce forests of southeast Alaska. Canadian Journal of Botany. 67(2): 318-326. [8931]

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Seed banking

More info for the terms: cover, density, frequency, litter

Several studies report that bunchberry seed is dormant upon maturity and requires cold stratification for germination. Bunchberry seed can remain viable in the soil seed bank for at least 3 years [282]. Several studies indicate that viable bunchberry seed occurs in the soil, but the quantity varies from no seed [7,89,266] up to 242 bunchberry seeds/ha [7]. Seed bank density does not seem to be associated with aboveground frequency (e.g., [6,7,266]). Differences among studies may be due to differences in seed production, which can be highly variable due to low light or late flowering; differences in seed predation (see Seed dispersal and Importance to wildlife); or differences in methodology used to determine seed bank composition [30].

In field studies conducted near Juneau, Alaska, emergence of bunchberry seedlings was monitored for seeds that were buried 0.4 inch (1 cm) below the forest floor in fine-mesh packets. Year 1 emergence ranged from 47% to 80%, year 2 emergence ranged from 18% to 53%, and year 3 emergence ranged from 1% to 16%. When ungerminated seeds were collected after a year of burial in the field, germination in the laboratory averaged 85% [282].

Seed bank studies in northeastern Minnesota suggested that bunchberry seed bank density may not correspond to the aboveground frequency of bunchberry. Only 4 bunchberry seeds/ha were extracted from soil samples collected in undisturbed jack pine stands where the aboveground frequency of bunchberry averaged 97%. Soil samples included the top 1 inch (2.5 cm) of mineral soil and surface litter layers [6]. In the Boundary Waters Canoe Area, no bunchberry seeds were extracted from soil samples collected from pine stands where the average aboveground frequency of bunchberry ranged from 27% to 67%. However, in a balsam fir stand where the aboveground frequency of bunchberry was only 3%, 242 bunchberry seeds/ha were extracted. Soil samples included the top 1 inch (2.5 cm) of mineral soil and the surface litter layers [7]. Samples of the top 1.2 inches (3 cm) of soil were taken from subalpine and low alpine white spruce forests in southern Quebec in early September. At both sites, aboveground cover of bunchberry averaged about 10% and 22 to 28 bunchberry seeds/m² were recovered [200].

Estimates of bunchberry seed bank density were low to none when researchers used the seedling emergence method [115,266], which may underestimate seed bank density [30]. When seedling emergence and seed extraction methods were compared for soil samples from a recently clearcut, mixed-deciduous forest in southern Ontario, no bunchberry seedlings emerged from soil samples in the greenhouse, but researchers successfully extracted almost 70 bunchberry seeds/m² from the soil. All soil samples were cold stratified then dried, and all roots and plant debris were removed from the samples [30].

Because the seedling emergence method may underestimate the density of bunchberry seed in the soil, the following studies may not reflect the true size of bunchberry seed banks. Bunchberry did not emerge from cold-stratified soil samples from disturbed or undisturbed Douglas-fir forests in south-central British Columbia. The frequency of bunchberry was about 15% in 2 of 8 sample sites [266]. Just 10 bunchberry seedlings/m² emerged from soil samples collected from old-growth, mixed-conifer forests in the HJ Andrews Experimental Forest in Oregon, where the aboveground cover of bunchberry averaged 9.4% [115]. In quaking aspen stands in northeastern Alberta, a small number of bunchberry seedlings (1.9/m²) emerged from unburned soil samples, but no seedlings emerged from soil collected from lightly or severely burned plots. Within about 2 years of burning, aboveground bunchberry cover averaged 3.2% on unburned, 7.6% on lightly burned, and 5.6% on severely burned plots [161].

The bunchberry seed bank may be limited to the upper soil layers. In jack pine- and white spruce-dominated stands in central Alberta, bunchberry seedlings did not emerge from mineral soil samples, but 22 seedlings/m² emerged from soil samples of the organic layer from a white spruce stand. Aboveground abundance of bunchberry was not reported [89].

  • 161. Lee, Philip. 2004. The impact of burn intensity from wildfires on seed and vegetative banks, and emergent understory in aspen-dominated boreal forests. Canadian Journal of Botany. 82(10): 1468-1480. [51462]
  • 6. Ahlgren, Clifford E. 1979. Buried seed in prescribe-burned jack pine forest soils, northeastern Minnesota. Minnesota Forestry Research Notes. No. 272. St. Paul, MN: University of Minnesota, College of Forestry. 3 p. [65922]
  • 7. Ahlgren, Clifford E. 1979. Buried seed in the forest floor of the Boundary Waters Canoe Area. Minnesota Forestry Research Notes No. 271. St. Paul, MN: University of Minnesota, College of Forestry. 4 p. [3459]
  • 30. Brown, Doug. 1992. Estimating the composition of a forest seed bank: a comparison of the seed extraction and seedling emergence methods. Canadian Journal of Botany. 70(8): 1603-1612. [69376]
  • 89. Fyles, James W. 1989. Seed bank populations in upland coniferous forests in central Alberta. Canadian Journal of Botany. 67: 274-278. [6388]
  • 115. Harmon, Janice M.; Franklin, Jerry F. 1995. Seed rain and seed bank of third- and fifth-order streams on the western slope of the Cascade Range. Res. Pap. PNW-RP-480. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Research Station. 27 p. [25915]
  • 200. Morin, Hubert; Payette, Serge. 1988. Buried seed populations in the montane, subalpine, and alpine belts of Mont Jacques-Cartier, Quebec. Canadian Journal of Botany. 66(1): 101-107. [6376]
  • 266. Stark, Kaeli E.; Arsenault, Andre; Bradfield, Gary E. 2006. Soil seed banks and plant community assembly following disturbance by fire and logging in interior Douglas-fir forests of south-central British Columbia. Canadian Journal of Botany. 84(10): 1548-1560. [65962]
  • 282. Tappeiner, J. C.; Alaback, P. B. 1989. Early establishment and vegetative growth of understory species in the western hemlock-Sitka spruce forests of southeast Alaska. Canadian Journal of Botany. 67(2): 318-326. [8931]

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Seed dispersal

More info for the term: fresh

Bunchberry fruits are consumed by many mammals and birds [69,248,299], and bunchberry seeds have been recovered from the feces of many species [58,86,129]. By early fall in central New Brunswick, 41% of bunchberry fruits were gone, 5% occurred beneath the parent plant, and the rest remained on plant (17% were whole, 33% were rotten, 4% were shriveled). The percentage of fruits removed from unprotected plants was 46.1% and from protected plants was 8.2% (P<0.001) [122]. In Newfoundland, researchers monitored the fate of bunchberry fruits and seeds for 3 fall seasons. Removal of fruits averaged 53%, damage by invertebrates averaged 23%, and fungal or microbe infection averaged 18%. Three percent of fruits were shriveled but remained on the plant, 2% of fruits were firm and remained on the plant, and 1% of fruits fell beneath the plant. Almost 6% of bunchberries were bitten off at the stem, suggesting removal by small mammals. Slugs were the major invertebrate feeders. Frugivores preferred intact, fresh berries; 92% of fruits removed were intact, and most fruits were taken within 5 weeks of ripening. American robins and white-throated sparrows fed on bunchberry fruits, and intact bunchberry seeds were recovered from ruffed grouse droppings. Field observations and exclusion experiments suggested that migratory birds were the primary bunchberry fruit predators or dispersers in Newfoundland [33]. Another study reported that white-throated sparrows may crush bunchberry seeds and may therefore be considered predators or poor dispersers (Thompson and Willson 1979 cited in [33]).
  • 58. Day, Susan Marie. 1997. Aspects of Newfoundland black bear (Ursus americanus hamiltoni) food habits and habitat use in human-influenced environments. Wolfville, NS: Acadia University. 107 p. Thesis. [83946]
  • 69. Ellison, Laurence. 1966. Seasonal foods and chemical analysis of winter diet of Alaskan spruce grouse. The Journal of Wildlife Management. 30(4): 729-735. [9735]
  • 129. Hungerford, Kenneth E. 1957. Evaluating ruffed grouse foods for habitat improvement. Transactions, 22nd North American Wildlife Conference. 22: 380-395. [15905]
  • 248. Schmidt, F. J. W. 1936. Winter food of the sharp-tailed grouse and pinnated grouse in Wisconsin. The Wilson Bulletin. 48(3): 186-203. [16729]
  • 299. Voss, Edward G. 1985. Michigan flora. Part II. Dicots (Saururaceae--Cornaceae). Bulletin 59. Bloomfield Hills, MI: Cranbrook Institute of Science; Ann Arbor, MI: University of Michigan Herbarium. 724 p. [11472]
  • 33. Burger, A. E. 1987. Fruiting and frugivory of Cornus canadensis in boreal forest in Newfoundland. Oikos. 49(1): 3-10. [8930]
  • 122. Helenurm, Kaius; Barrett, Spencer C. H. 1987. The reproductive biology of boreal forest herbs. II. Phenology of flowering and fruiting. Canadian Journal of Botany. 65(10): 2047-2056. [6623]
  • 86. Francis, George Reid. 1958. Ecological studies of marten, Martes americana, in Algonquin Park, Ontario. Vancouver, BC: University of British Columbia. 74 p. [+ appendices]. Thesis. [76922]

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Seed production

More info for the terms: cover, tree

Studies often report poor seed production by bunchberry; however, seed production may increase with increased light availability. Weather conditions and flowering date can also affect seed production. While the age at which wild-growing bunchberry plants produce flowers and fruits was not reported in the available literature (as of 2011), in a nursery setting, bunchberry plants grown from seed took 5 years to produce flowers [73].

Photo © Joy Viola, Northeastern University, Bugwood.org

Several studies suggest that bunchberry seed production is greater in high-light than low-light environments. In the Chugach National Forest on the Kenai Peninsula, bunchberry fruit production increased with tree morality from spruce beetle infestations. Regression analyses revealed that the number of fruits produced decreased by a factor of 0.84 with every 10% increase in canopy cover. When data were pooled from all study plots regardless of beetle infestation levels, bunchberry fruit production was greatest (35.3 berries/m²) in white spruce stands and least (10.6 berries/m²) in mountain hemlock stands [278]. In Itasca State Park, Minnesota, bunchberry was typically found in a vegetative state in densely shaded areas of jack pine-white spruce-balsam fir forests. Only 3.1% of plants were found in a flowering or fruiting state where light intensity averaged 16% of full sun [94]. At the Enterprise Radiation Site in Oneida County, Wisconsin, bunchberry flowers were rare in a woodland, but up to 15.6% of bunchberry shoots were flowering at an open-canopy site. However, fruit set was low at all sites, and seed viability was very low [14]. Over 4 growing seasons in the Sitka spruce-western hemlock zone of southeastern Alaska, seed production by understory species was compared in clearcut, second-growth, and old-growth stands. Cornus spp. fruit production in clearcuts was 400 times the production in old-growth stands. No fruit was produced by any understory species in areas where solar transmissivity was 3% or less [9].

Abundance and size of bunchberry fruits can vary with seasonal conditions and time of year. During wet, cool conditions in central New Brunswick, duration of bunchberry flower production was reduced, and late-developing flowers had low fruit set. During the 1st growing season in the spruce-fir study area, conditions were warm and dry, and bunchberry flowered for 26 days; in the 2nd growing season, conditions were cool and wet, and bunchberry flowered for 18 days. The number of days from the 1st open flowers to peak flowering was 6 days shorter in the cool, wet growing season. From a total of 207 bunchberry plants, 5,221 flower buds were produced. Nearly 87% of flowers opened and almost 11% produced mature fruit. Fruit set was best (almost 20%) for flowers produced at the initial or early flowering periods; fruit set was less (nearly 9%) for flowers produced at peak flowering time. Fruit set was poor to nonexistent (≤1.6%) for flowers produced near or at the end of the flowering period [122]. In Kings County, Nova Scotia, bunchberry fruits were sampled from 25 shoots at 2 times in a single growing season. Fruits sampled at the end of July averaged 11.8 per inflorescence and 0.077 g/fruit; fruits sampled in mid-September averaged 9.2 per inflorescence and 0.149 g/fruit [103]. It was unclear if sampled shoots were protected and whether or not the reduction in fruits/inflorescence reflects both herbivory and maturation events.

In the southernmost bunchberry population, a relatively dry site in Albemarle County, Virginia, plants produced no fruits in 5 years of observation. About 10% of plants produced flowers but none developed into fruits. The author did not speculate about the prevailing cause of fruit failure [268].

  • 14. Armentano, Thomas Vincent. 1973. Population ecology and response to stress of Aster macrophyllus and Cornus canadensis. Chapel Hill, NC: University of North Carolina at Chapel Hill. 211 p. Dissertation. [83945]
  • 103. Hall, Ivan V.; Sibley, Jack D. 1976. The biology of Canadian weeds. 20. Cornus canadensis L. Canadian Journal of Plant Science. 56(4): 885-892. [83881]
  • 268. Stevens, Charles E. 1968. A remarkable disjunct occurrence of Cornus canadensis in the Virginia Blue Ridge. Castanea. 33(3): 247-248. [83933]
  • 73. Feng, Chun-Miao; Qu, Rongda; Zhou, Li-Li; Xie, De-Yu; Xiang, Qiu-Yun (Jenny). 2009. Shoot regeneration of dwarf dogwood (Cornus canadensis L.) and morphological characterization of the regenerated plants. Plant Cell, Tissue and Organ Culture. 97(1): 27-37. [83880]
  • 94. Good, Norma Frauendorf. 1963. Reproduction and productivity patterns in a pine-spruce-fir community in Itasca Park, Minnesota. Bulletin of the Torrey Botanical Club. 90(5): 287-292. [61333]
  • 122. Helenurm, Kaius; Barrett, Spencer C. H. 1987. The reproductive biology of boreal forest herbs. II. Phenology of flowering and fruiting. Canadian Journal of Botany. 65(10): 2047-2056. [6623]
  • 278. Suring, Lowell H.; Goldstein, Michael I.; Howell, Susan; Nations, Christopher S. 2006. Effects of spruce beetle infestations on berry productivity on the Kenai Peninsula, Alaska. Forest Ecology and Management. 227(3): 247-256. [62653]
  • 9. Alaback, Paul B.; Tappeiner, John C., II. 1986. Seed and fruit production of forest understory plants in coastal Alaska. In: Proceedings, 67th annual meeting of the Pacific Division, American Association for the Advancement of Science and the 1986 meeting of the arctic science conference (Arctic Division, American Association for the Advancement of Science); 1986 June 8-13; Vancouver, BC. Volume 5, part 1. [San Francisco, CA]: Pacific Division, American Association for the Advancement of Science: 20. Abstract. [83874]

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Pollination and breeding system

More info for the term: perfect

Bunchberry produces perfect flowers [11,251] that are self incompatible and insect pollinated [103]. Self fertilization of bunchberry flowers is prevented by protandry. Bees and flies commonly visit bunchberry flowers, and an extensive list of insect visitors was recorded by Lovell [172]. In central New Brunswick, the number of insect visits to bunchberry flowers was "relatively high" among the 12 understory species observed in the area. When flowers were bagged to exclude insect visitors, virtually no bunchberry fruit was set. In controlled experiments, 21.5% of cross-pollinated flowers set fruit, 10.7% of open-pollinated flowers set fruit, but no self-pollinated flowers set fruit. Low fruit set for cross-pollinated flowers suggested that bunchberry aborts fruits as resources become limited [18]. Wind pollination of bunchberry flowers was suspected in Isle Royale National Park, after researchers protected flowers from insects and found that 3 of 9 protected inflorescences produced seed. Seed production was greater for unprotected inflorescences [310].

Bunchberry flowers are equipped with an appendage that explosively releases pollen when touched [70,172,222]. Researchers recorded and studied explosive pollen release from bunchberry plants collected from relatively undisturbed forest habitat in Isle Royale National Park. When the flower appendage was touched, pollen was launched straight upward at high speeds. Bunchberry pollen was carried over 8.7 inches (22 cm) in a room with minor air currents. Researchers calculated that any wind speed greater than 0.4 feet (0.12 m)/second was sufficient to transport bunchberry pollen. The speed of pollen release was sufficient to lodge pollen into an insect's hairs, and in the field, insects that triggered flower explosions were coated with pollen [310].

  • 11. Anderson, J. P. 1959. Flora of Alaska and adjacent parts of Canada. Ames, IA: Iowa State University Press. 543 p. [9928]
  • 18. Barrett, Spencer C.; Helenurm, Kaius. 1987. The reproductive biology of boreal forest herbs. I. Breeding systems and pollination. Canadian Journal of Botany. 65(10): 2036-2046. [6624]
  • 103. Hall, Ivan V.; Sibley, Jack D. 1976. The biology of Canadian weeds. 20. Cornus canadensis L. Canadian Journal of Plant Science. 56(4): 885-892. [83881]
  • 222. Pojar, Jim; MacKinnon, Andy, eds. 1994. Plants of the Pacific Northwest coast: Washington, Oregon, British Columbia and Alaska. Redmond, WA: Lone Pine Publishing. 526 p. [25159]
  • 70. Eyde, Richard H. 1988. Comprehending Cornus: puzzles and progress in the systematics of the dogwoods. Botanical Review. 54(3): 233-351. [6144]
  • 251. Scoggan, H. J. 1978. The flora of Canada. Part 4: Dicotyledoneae (Dictoyledonceae to Compositae). National Museum of Natural Sciences: Publications in Botany, No. 7(4). Ottawa: National Museums of Canada. 1711 p. [78054]
  • 172. Lovell, John H. 1898. The insect-visitors of flowers. Bulletin of the Torrey Botanical Club. 25(7): 382-390. [83926]
  • 310. Whitaker, D. L.; Webster, L. A.; Edwards, J. 2007. The biomechanics of Cornus canadensis stamens are ideal for catapulting pollen vertically. Functional Ecology. 21(2): 219-225. [83939]

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Regeneration Processes

More info for the terms: breeding system, top-kill

Bunchberry regenerates by seed and rhizomes. Sprouting from rhizomes is its primary regeneration method following top-kill [37,173]. Clonal growth is important to bunchberry's long-term persistence in densely shaded, late-seral forests where flowering is rare [9,14,94].

  • 14. Armentano, Thomas Vincent. 1973. Population ecology and response to stress of Aster macrophyllus and Cornus canadensis. Chapel Hill, NC: University of North Carolina at Chapel Hill. 211 p. Dissertation. [83945]
  • 173. Lynham, T. J.; Curran, T. R. 1998. Vegetation recovery after wildfire in old-growth red and white pine. Frontline: Forestry Research Applications/Technical Note No. 100. Sault Ste. Marie, ON: Natural Resources Canada, Canadian Forest Service, Great Lakes Forestry Centre. 4 p. [30685]
  • 37. Chapman, Rachel Ross; Crow, Garrett E. 1981. Application of Raunkiaer's life form system to plant species survival after fire. Bulletin of the Torrey Botanical Club. 108(4): 472-478. [617]
  • 94. Good, Norma Frauendorf. 1963. Reproduction and productivity patterns in a pine-spruce-fir community in Itasca Park, Minnesota. Bulletin of the Torrey Botanical Club. 90(5): 287-292. [61333]
  • 9. Alaback, Paul B.; Tappeiner, John C., II. 1986. Seed and fruit production of forest understory plants in coastal Alaska. In: Proceedings, 67th annual meeting of the Pacific Division, American Association for the Advancement of Science and the 1986 meeting of the arctic science conference (Arctic Division, American Association for the Advancement of Science); 1986 June 8-13; Vancouver, BC. Volume 5, part 1. [San Francisco, CA]: Pacific Division, American Association for the Advancement of Science: 20. Abstract. [83874]

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Growth Form (according to Raunkiær Life-form classification)

More info on this topic.

More info for the term: hemicryptophyte

Raunkiaer [228] life form:
Hemicryptophyte
  • 228. Raunkiaer, C. 1934. The life forms of plants and statistical plant geography. Oxford: Clarendon Press. 632 p. [2843]

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Life Form

More info for the terms: forb, shrub

Forb-shrub

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Fire Regime Table

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Seedling establishment and plant growth

Bunchberry seedling establishment and plant growth were not well documented in the available literature (as of 2011). Factors that are favorable or unfavorable to bunchberry seedling establishment are unknown or have gone unreported. In southeastern Alaska, bunchberry seedling survival averaged 13% in 3 to 4 years after experimental seeding in western hemlock-Sitka spruce stands [282]. After surveying numerous bunchberry habitats in Nova Scotia for 2 summers, researchers found no bunchberry seedlings. One of the summers was very dry [103].
  • 103. Hall, Ivan V.; Sibley, Jack D. 1976. The biology of Canadian weeds. 20. Cornus canadensis L. Canadian Journal of Plant Science. 56(4): 885-892. [83881]
  • 282. Tappeiner, J. C.; Alaback, P. B. 1989. Early establishment and vegetative growth of understory species in the western hemlock-Sitka spruce forests of southeast Alaska. Canadian Journal of Botany. 67(2): 318-326. [8931]

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Life History and Behavior

Cyclicity

Phenology

More info on this topic.

Throughout its range, bunchberry flowering is most typical from May to July [186,241,261,272]. However, flowering may be delayed on cold, exposed sites [299]. In the Adirondack Uplands of New York, the earliest bunchberry flowering date was 26 May, and the latest was 19 October [145].

Bunchberry fruits are common near the end of summer but can occur anytime from July to October [145,178,261,299]. In the Canadian Arctic, bunchberry produced both flowers and fruits within 6 to 7 weeks [103].

The percentage of nonstructural carbohydrates in bunchberry rhizomes increased from spring to fall in Nova Scotia. The dry weight of nonstructural carbohydrates was 5% to 10% for rhizomes collected in the spring, a little more than 15% in the summer, and a little less than 20% in the fall [76].

  • 103. Hall, Ivan V.; Sibley, Jack D. 1976. The biology of Canadian weeds. 20. Cornus canadensis L. Canadian Journal of Plant Science. 56(4): 885-892. [83881]
  • 145. Kudish, Michael. 1992. Adirondack upland flora: an ecological perspective. Saranac, NY: The Chauncy Press. 320 p. [19376]
  • 178. Magee, Dennis W.; Ahles, Harry E. 2007. Flora of the Northeast: A manual of the vascular flora of New England and adjacent New York. 2nd ed. Amherst, MA: University of Massachusetts Press. 1214 p. [74293]
  • 186. Martin, William C.; Hutchins, Charles R. 1981. A flora of New Mexico. Volume 2. Germany: J. Cramer. 2589 p. [37176]
  • 241. Roland, A. E.; Smith, E. C. 1969. The flora of Nova Scotia. Halifax, NS: Nova Scotia Museum. 746 p. [13158]
  • 261. Soper, James H.; Heimburger, Margaret L. 1982. Shrubs of Ontario. Life Sciences Miscellaneous Publications. Toronto, ON: Royal Ontario Museum. 495 p. [12907]
  • 272. Strausbaugh, P. D.; Core, Earl L. 1977. Flora of West Virginia. 2nd ed. Morgantown, WV: Seneca Books. 1079 p. [23213]
  • 299. Voss, Edward G. 1985. Michigan flora. Part II. Dicots (Saururaceae--Cornaceae). Bulletin 59. Bloomfield Hills, MI: Cranbrook Institute of Science; Ann Arbor, MI: University of Michigan Herbarium. 724 p. [11472]
  • 76. Flinn, Marguerite A.; Fisher, Sharon E.; Martin, Earl V.; Blum, Ilya E. 1985. Seasonal variation in the nonstructural carbohydrate composition of rhizomes of forest understory species. Proceedings of the Nova Scotian Institute of Science. 35: 91-97. [10488]

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Flowering from July to August; fruiting from August to September.
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© Wen, Jun

Source: Plants of Tibet

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Evolution and Systematics

Evolution

The phylogenetic relationships of Cornus has been inferred using nuclear gene 26S rDNA (Fan and Xiang, 2001). The 26S rDNA sequence data suggested that Cornus Canadensis is closely related to C. unalaschkensis.
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© Wen, Jun

Source: Plants of Tibet

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Functional Adaptations

Functional adaptation

Pollen catapults from flower: bunchberry
 

Pollen from bunchberry flowers are dispersed by release of stored elastic energy.

         
  "[W]e describe how the flower stamens of the bunchberry dogwood (Cornus canadensis) rely on this principle [release of stored elastic energy] to catapult pollen into the air as the flower opens explosively. Our high-speed video observations show that the flower opens in less than 0.5 ms — to our knowledge, the fastest movement so far recorded in a plant.
 
"Cornus canadensis grows in dense carpets in the vast spruce-fir forests of the North American taiga. As bunchberry flowers burst open, their petals rapidly separate and flip back to release the stamens (Fig. 1). During the first 0.3 ms, the stamens accelerate at up to 24,000 + or - 6,000 m/s2 (2,400g), reaching the high speed (3.1+ or - 0.5 m/s) necessary to propel pollen, which is light and rapidly decelerated by air resistance (terminal velocity, 0.12 + or - 0.03m/s(mean = or - s.e.m.);n=7).The
 pollen granules are launched to an impressive height of 2.5 cm (range, 2.2–2.7 cm; n=5), which is more than ten times the height of the flower: from this height, they can be carried away by the wind."

"Bunchberry stamens are designed like miniature medieval trebuchets — specialized catapults that maximize throwing distance by having the payload (pollen in the anther) attached to the throwing arm (filament) by a
hinge or flexible strap (thin vascular strand connecting the anther to the filament tip). This floral trebuchet enables stamens to propel pollen upwards faster than would a simple catapult. After the petals open, the bent filaments unfold,releasing elastic energy.The tipof the filament follows an arc,but the rotation of the anther about the filament tip allows it to accelerate pollen upwards to its maximum vertical speed, and the pollen is released only as it starts to accelerate horizontally. (Edwards et al. 2005:164)


  Learn more about this functional adaptation.
  • Edwards, J., Whitaker, D., Klionsky, S., & Laskowski, M. 2005. A record-breaking pollen catapult. Nature. 435: 164.
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Molecular Biology and Genetics

Genetics

There are some reports for the chromosomal data of Cornus canadensis. All counts are 2n = 22, 44 (Brain and Denford, 1979; Plante, 1995; Gervais et al., 1999).
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Molecular Biology

Barcode data: Cornus canadensis

The following is a representative barcode sequence, the centroid of all available sequences for this species.


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© Barcode of Life Data Systems

Source: Barcode of Life Data Systems (BOLD)

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Statistics of barcoding coverage: Cornus canadensis

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 8
Specimens with Barcodes: 27
Species With Barcodes: 1
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Conservation

Conservation Status

Information on state- and province-level protection status of plants in the United States and Canada is available at NatureServe.

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National NatureServe Conservation Status

Canada

Rounded National Status Rank: N5 - Secure

United States

Rounded National Status Rank: N5 - Secure

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NatureServe Conservation Status

Rounded Global Status Rank: G5 - Secure

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Threats

Comments: Land-use conversion, habitat fragmentation, and forest management practices are low-level threats to this species (Southern Appalachian Species Viability Project 2002).

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Management

Management considerations

Experimental findings suggest that bunchberry may improve conditions in areas impacted by acid rain. When 4 boreal forest understory species were compared, bunchberry leaves neutralized experimental acid rain treatments most [90].
  • 90. Gaber, B. A.; Hutchinson, T. C. 1988. The neutralization of acid rain by the leaves of four boreal forest species. Canadian Journal of Botany. 66(9): 1877-1882. [8872]

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Relevance to Humans and Ecosystems

Benefits

Importance to Livestock and Wildlife

More info for the terms: cover, frequency

Bunchberry can be an important forage species for caribou, moose, elk, and deer [15,53,140,249,298]. Bunchberry fruits are utilized by bears, small mammals, and many bird species [181,250,299]. Bunchberry does not appear to be a food source for cattle [140].

Ungulates: A variety of large ungulates in northern North America utilize bunchberry. Caribou dig through snow to feed on bunchberry in the winter in British Columbia (review in [141]). On the Slate Islands of Lake Superior in Ontario, caribou frequently feed on bunchberry in the spring [53]. Two out of 20 rumens from caribou taken from the Northwest Territories, northern Saskatchewan, and northern Manitoba had bunchberry, and weight of bunchberry was only a trace of the contents recovered [252]. Reviews report that bunchberry is eaten by moose [15,232]. When researchers observed feeding by 3 tame moose on Kenai Peninsula, bunchberry was occasionally eaten from May to October [165]. On Brunette Island, Newfoundland, 15% of the bites taken by a tame moose over 50 minutes were from bunchberry and Lapland cornel [34]. In eastern Maine, bunchberry was early winter moose forage [160]. A review reports that the average percentage of bunchberry in the diets of elk in British Columbia and Washington was greatest in the summer (5.4%) and fall (3.9%). Bunchberry was much less common in winter (0.5%) and spring (1.4%) diets [134]. In northern Idaho, elk and white-tailed deer fed on bunchberry more in grand fir than western redcedar forests. In grand fir forests, the composition of early fall diets for elk and white-tailed deer averaged 7.4% and 8.7% bunchberry, respectively. Bunchberry was not a part of mid-summer elk diets and made up only 3.6% of white-tailed deer diets in mid-summer [140].

Deer use of bunchberry can be extensive. Bunchberry is considered highly preferred and is highly digestible by mule deer in British Columbia and Alaska [212]. In western hemlock forests on warm winter-use areas of the Tongass National Forest, Alaska, severe browsing by mule deer can result in the "virtual elimination" of bunchberry from the understory [184]. Mule deer feces collected from Admiralty Island in southeastern Alaska were 33%, 26%, 14%, and 19% bunchberry in the winter, spring, summer, and fall, respectively [111]. In the Upper Swan Valley of northwestern Montana, bunchberry was an important component of white-tailed deer diets in the fall [203,204]. On a reclaimed mine site in west-central Alberta, white-tailed deer and mule deer feces contained 31.2% bunchberry, but no bunchberry was recovered from moose feces collected from the same area [239]. Bunchberry made up at least 4% of the rumen contents from 14 white-tailed deer killed in northeastern Minnesota [308]. On Anticosti Island, Quebec, bunchberry was significantly (P<0.05) associated with fenced areas of a clearcut located 79 to 3,020 feet (24-919 m) from the edge of a balsam fir-spruce forest. White-tailed deer and snowshoe hares were excluded by fencing. Immediately after cutting, bunchberry cover averaged 2.9% in fenced and 1.1% in unfenced areas; 8 years after cutting, cover averaged 9.8% in fenced and 1.6% in unfenced areas [36].

Bear: Bunchberry fruits are eaten by black bears from Alaska and Oregon to Newfoundland. Use may be greatest in the late summer or fall. On the Kenai Peninsula, bunchberry frequency and volume in fall black bear diets were 5.9% and 37.5%, respectively, in a northern coniferous forest that had burned 10 to 15 years earlier. Bunchberry was not found in spring or summer black bear diets or in scat collected on a less recently burned forest area [250]. In fecal samples collected in northeastern Oregon, bunchberry fruits made up 4% or less of the volume of black bear diets [32]. In black bear scat collected from spring through fall in Gros Morne National Park and Terra Nova National Park in Newfoundland, the frequency of bunchberry ranged from 0% to 15.7%. Scat was collected for 3 to 4 years. Frequency of bunchberry was greater in late-summer and fall collections than spring-summer collections, and in one year, no bunchberry was recovered in any season [58].

Small mammals: Chipmunks, martens, cottontails, and snowshoe hares feed on bunchberry stems and fruits [284,299,306,313]. In Michigan, chipmunks presented bunchberry fruits fed on them "eagerly" (Gorchov personal communication cited in [262]). Bunchberry was not recovered from all marten scat collected over a 6-year period in northwestern Glacier National Park, but a high of 3.6% bunchberry was recovered from one collection [306]. Marten scat collected from Algonquin Park, Ontario, occasionally contained bunchberry seeds; however, when a released marten was observed feeding, it ignored ripe bunchberries [86]. In western Massachusetts, damage to bunchberry was rated as severe after 6 years of eastern cottontail feeding [281]. In the winter near Syracuse, New York, eastern cottontails fed "sparingly" on bunchberry [284]. Based on the analysis of stomach contents, the diet of snowshoe hares near Fairbanks, Alaska, was 1.8% bunchberry in April, 2.6% in May, and 1% in the fall [313].

Birds: Bunchberry is utilized by song and game birds. Bunchberry fruits are eaten by thrushes, veeries, vireos, and grouse [181]. In Alaska, the occurrence of bunchberry flowers in the crops of spruce grouse was 4.3% in the spring, and the occurrence of bunchberry fruits was 3.9% in September and 9.3% in October [69]. From ruffed grouse droppings collected from the University of Idaho's Experimental Forest in Latah County, researchers determined that utilization of bunchberry seeds averaged 13% in the last half of July, 27% in the first half of August, and 29% in the last half of August. Availability of bunchberry averaged 23% [129]. Ruffed grouse fed on bunchberry in the spring in the boreal forest region of northern Minnesota [279], and sharp-tailed grouse fed on bunchberry fruits in the winter in Quebec [248]. Other researchers report that bunchberry is often found in the vegetation surrounding American woodcock nests [194].

Palatability and nutritional value: Palatability information was generally unavailable as of 2011. After reviewing the available literature, Strong and Gates [274] suggested that the preference rating for bunchberry was low for elk and low to moderate for moose.

Digestibility and nutritional content of bunchberry vary with season and site conditions. In Sitka spruce-western hemlock forests in southeastern Alaska, the 48-hour digestibility of bunchberry averaged 65.9%, and bunchberry was most digestible in the winter [110]. Based on captive feeding trials for black bears and grizzly bears, researchers determined that the dry matter digestibility of bunchberry fruits was 45.6% [307]. In southeastern Alaska, the chemical composition of bunchberry leaves varied significantly with stand age and season (P<0.001). Generally, nitrogen and potassium levels were greater in older than younger stands and decreased from spring to fall. Nonstructural carbohydrate and astringency levels increased with increasing stand age [293]. Studies from the same region reported that bunchberry from an old-growth forest had significantly greater nitrogen content and digestibility than bunchberry from scrub stands (Schoen and Kirchhoff 1984 cited in [249]) and that protein content of bunchberry leaves was 27% greater from a forest site than an adjacent clearcut (personal observation cited in [234]). The average crude protein content of bunchberry pulp was 4.3% and of seed was 10% from fruits collected in Idaho, Washington, Montana, and/or Alaska [307]. Bunchberry fruits collected from northern Ontario had fat, protein, and soluble carbohydrate levels intermediate among the 16 other species evaluated [291]. On Admiralty Island, Alaska, bunchberry was considered an important and nutritious winter food for mule deer [249]. For a comparison of the seasonal composition of bunchberry in southeastern Alaska, see Hanley and McKendrick [110], and for a comparison of the chemical composition of bunchberry in New Hampshire, Wisconsin, and Canada, see Siccama and others [256].

  • 15. Ayotte, Jeremy B.; Parker, Katherine L.; Arocena, Joselito M.; Gillingham, Michael P. 2006. Chemical composition of lick soils: functions of soil ingestion by four ungulate species. Journal of Mammalogy. 87(5): 878-888. [78499]
  • 32. Bull, Evelyn L.; Torgersen, Torolf R.; Wertz, Tara L. 2001. The importance of vegetation, insects, and neonate ungulates in black bear diet in northeastern Oregon. Northwest Science. 75(3): 244-253. [67680]
  • 34. Butler, C. E. 1986. Summer food utilization and observations of a tame moose Alces alces. The Canadian Field-Naturalist. 100: 85-88. [8871]
  • 36. Casabon, Christine; Pothier, David. 2008. Impact of deer browsing on plant communities in cutover sites on Anticosti Island. Ecoscience. 15(3): 389-397. [83878]
  • 53. Cringan, Alexander Thom. 1957. History, food habits and range requirements of the woodland caribou of continental North America. In: Transactions, 22nd North American wildlife conference; 1957 March 4-6; Washington, DC. Washington, DC: Wildlife Management Institute: 485-501. [15651]
  • 58. Day, Susan Marie. 1997. Aspects of Newfoundland black bear (Ursus americanus hamiltoni) food habits and habitat use in human-influenced environments. Wolfville, NS: Acadia University. 107 p. Thesis. [83946]
  • 69. Ellison, Laurence. 1966. Seasonal foods and chemical analysis of winter diet of Alaskan spruce grouse. The Journal of Wildlife Management. 30(4): 729-735. [9735]
  • 111. Hanley, Thomas A.; Robbins, Charles T.; Spalinger, Donald E. 1989. Forest habitats and the nutritional ecology of Sitka black-tailed deer: a research synthesis with implications for forest management. Gen. Tech. Rep. PNW-GTR-230. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Research Station. 52 p. [7509]
  • 129. Hungerford, Kenneth E. 1957. Evaluating ruffed grouse foods for habitat improvement. Transactions, 22nd North American Wildlife Conference. 22: 380-395. [15905]
  • 134. Jenkins, Kurt J.; Starkey, Edward E. 1991. Food habits of Roosevelt elk. Rangelands. 13(6): 261-265. [17351]
  • 140. Kingery, James L.; Mosley, Jeffrey C.; Bordwell, Kirsten C. 1996. Dietary overlap among cattle and cervids in northern Idaho forests. Journal of Range Management. 49(1): 8-15. [26611]
  • 141. Kinley, Trevor A.; Bergenske, John; Davies, Julie-Anne; Quinn, David. 2003. Characteristics of early-winter caribou, Rangifer tarandus caribou, feeding sites in the southern Purcell Mountains, British Columbia. The Canadian Field-Naturalist. 117(3): 352-359. [65798]
  • 160. Lautenschlager, R. A.; Crawford, H. S.; Stokes, M. R.; Stone, T. L. 1997. Forest disturbance type differentially affects seasonal moose forage. Alces. 33: 49-73. [78861]
  • 165. LeResche, Robert E.; Davis, James L. 1973. Importance of nonbrowse foods to moose on the Kenai Peninsula, Alaska. The Journal of Wildlife Management. 37(3): 279-287. [13123]
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  • 184. Martin, Jon R.; Trull, Susan J.; Brady, Ward W.; West, Randolph A.; Downs, Jim M. 1995. Forest plant association management guide: Chatham Area, Tongass National Forest. R10-TP-57. Juneau, AK: U.S. Department of Agriculture, Forest Service, Alaska Region. Variously paginated. [67100]
  • 194. Mendall, Howard L.; Aldous, Clarence M. 1943. The ecology and management of the American woodcock. Orono, ME: Maine Cooperative Wildlife Research Unit. 201 p. [73807]
  • 203. Mundinger, John D. 1978. Population ecology and habitat relationships of white-tailed deer in coniferous forest habitat of northwestern Montana. Montana deer studies: Job progress report 1977-1978. Helena, MT: Montana Department of Fish and Game. 74 p. [21525]
  • 204. Mundinger, John G. 1979. Population ecology and habitat relationships of white-tailed deer in coniferous forest habitat of northwestern Montana. Montana deer studies: Job progress report 1978-1979. Helena, MT: Montana Department of Fish and Game. 65 p. [21526]
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  • 232. Renecker, Lyle A.; Schwartz, Charles C. 2007. Food habits and feeding behavior. In: Franzmann, Albert W.; Schwartz, Charles C.; McCabe, Richard E., eds. Ecology and management of the North American moose. 2nd ed. Boulder, CO: University Press of Colorado: 403-440. [79106]
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Other uses and values

Although edible, bunchberry fruits are nearly flavorless [68,145]. They have been important in the diets of Eskimos of the Northern Bering Sea and Arctic regions of Alaska [10], Indians of the Nuxalk Nation in British Columbia [164], and Coast Salish Indians on Vancouver Island [288]. Bunchberry leaves have been smoked as a tobacco substitute. A tea from bunchberry roots has been used to treat colic in infants. In ancient Scotland, bunchberry was referred to as the "plant of gluttony" because it was thought to increase the appetite [238]. The Hoh and Quileute Indians of the Olympic peninsula used bunchberry fruits in ceremonies, bunchberry bark in medicinal teas, and bunchberry leaves as an intoxicating smoke [230].
  • 145. Kudish, Michael. 1992. Adirondack upland flora: an ecological perspective. Saranac, NY: The Chauncy Press. 320 p. [19376]
  • 10. Anderson, J. P. 1939. Plants used by the Eskimo of the Northern Bering Sea and Arctic regions of Alaska. American Journal of Botany. 26(9): 714-716. [55594]
  • 68. Elias, Thomas S.; Dykeman, Peter A. 1982. Field guide to North American edible wild plants. New York: Outdoor Life Books. 286 p. [21103]
  • 164. Lepofsky, Dana; Turner, Nancy J.; Kuhnlein, Harriet V. 1985. Determining the availability of traditional wild plant foods: an example of Nuxalk foods, Bella Coola, British Columbia. Ecology of Food and Nutrition. 16: 223-241. [7002]
  • 230. Reagan, Albert B. 1934. Plants used by the Hoh and Quileute Indians. Transactions of the Kansas Academy of Science. 37: 55-70. [66487]
  • 238. Robuck, O. Wayne. 1985. The common plants of the muskegs of southeast Alaska. Miscellaneous Publication/July 1985. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station. 131 p. [11556]
  • 288. Turner, Nancy Chapman; Bell, Marcus A. M. 1971. The ethnobotany of the Coast Salish Indians of Vancouver Island. Economic Botany. 25(3): 63-104. [21014]

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Wikipedia

Cornus canadensis

Cornus canadensis (Canadian dwarf cornel, Canadian bunchberry, quatre-temps, crackerberry, creeping dogwood) is a species of flowering plant in the Cornaceae (dogwood) family, native to eastern Asia (Japan, Korea, northeastern China (Jilin Province) and the Russian Far East), northern USA, Colorado, New Mexico, Canada and Greenland.[1] Unlike its relatives, which are for the most part substantial trees and shrubs, C. canadensis is a creeping, rhizomatous perennial growing to about 20 cm (8 in) tall.

Taxonomy[edit]

While distinctive as a species itself, the generic placement of these plants has differed in various botanical treatments. When the genus Cornus is taken broadly, as done here, this species is Cornus canadensis. However, if Cornus is treated in a narrower sense, excluding this species, it can instead be classified as Chamaepericlymenum canadense or as Cornella canadensis.[2][3]

Where bunchberry, a forest species, and Cornus suecica, a bog species, grow near each other in their overlapping ranges in Alaska, Labrador, and Greenland, they can hybridize by cross-pollination, producing plants with intermediate characteristics.[4]

Description[edit]

Cornus canadensis is a slow-growing herbaceous subshrub growing 10–20 cm tall, generally forming a carpet-like mat. The above-ground shoots rise from slender creeping rhizomes that are placed 2.5–7.5 cm deep in the soil, and form clonal colonies under trees. The vertically produced above-ground stems are slender and unbranched. The leaves are oppositely arranged on the stem, but are clustered with six leaves that often seem to be in a whorl because the internodes are compressed. The leafy green leaves are produced near the terminal node and consist of two types: 2 larger and 4 smaller leaves. The smaller leaves develop from the axillary buds of the larger leaves. The shiny dark green leaves have 2 to 3 mm long petioles and leaf blades that are obovate. The blades have entire margins and are 3.5 to 4.8 cm long and 1.5 to 2.5 cm wide, with 2 or 3 veins and cuneate shaped bases and abruptly acuminate apexes. In the fall, the leaves have red tinted veins and turn completely red.

Flowers[edit]

Mature and immature flowers, Bonnechere Provincial Park, Ontario

In late spring to midsummer, white flowers are produced that are 2 mm (0.079 in) in diameter with reflexed petals that are ovate-lanceolate in shape and 1.5–2 cm (0.59–0.79 in) long. Inflorescences are made up of compound terminal cymes, with large showy white bracts. The bracts are broadly ovate and 0.8 to 1.2 cm long and 0.5 to 1.1 cm wide, with 7 parallel running veins. The lower nodes on the stem have greatly reduced rudimentary leaves. The calyx tube is obovate in shape and 1 mm long covered with densely pubescent hairs along with grayish white appressed trichomes. Stamens are very short, being 1 mm long. The anthers are yellowish white in color, narrowly ovoid in shape. The styles are 1 mm long and glabrous. Plants are for the most part self-sterile and dependent on pollinators for sexual reproduction. Pollinators include bumblebees, solitary bees, beeflies, and syrphid flies.[5] The fruits look like berries but are drupes.

Release of pollen[edit]

Each flower has highly elastic petals that flip backward, releasing springy filaments that are cocked underneath the petals. The filaments snap upward flinging pollen out of containers hinged to the filaments. This motion takes place in less than half a millisecond and the pollen experiences two to three thousand times the force of gravity.[6] The Bunchberry has one of the fastest plant actions found so far requiring a camera capable of shooting 10,000 frames per second to catch the action.[7]

Fruit[edit]

Fruit

The drupes are green, globose in shape, turning bright red at maturity in late summer; each fruit is 5 mm in diameter and contains typically one or two ellipsoid-ovoid shaped stones. The fruits are edible with a mild flavour somewhat like apples. The large seeds within are somewhat hard and crunchy.

Ecology[edit]

Birds are the main dispersal agents of the seeds, consuming the fruit during their fall migration. In Alaska, bunchberry is an important forage plant for mule deer, black-tailed deer and moose, which consume it throughout the growing season.[8]

Habitat[edit]

Cornus canadensis is a mesophytic species that needs cool, moist soils. It inhabits montane and boreal coniferous forests, where it is found growing along the margins of moist woods, on old tree stumps, in mossy areas, and amongst other open and moist habitats.

References[edit]

  1. ^ RHS A-Z encyclopedia of garden plants. United Kingdom: Dorling Kindersley. 2008. p. 1136. ISBN 1405332964. 
  2. ^ Eyde, R. H. 1987. The case for keeping Cornus in the broad Linnaean sense. Systematic Botany. 12(4): 505-518.
  3. ^ Eyde, Richard H. 1988. Comprehending Cornus: puzzles and progress in the systematics of the dogwoods. Botanical Review. 54(3): 233-351.
  4. ^ Neiland, Bonita J. 1971. The forest-bog complex of southeast Alaska. Vegetatio. 22: 1-64.
  5. ^ Barrett, Spencer C.; Helenurm, Kaius. 1987. The reproductive biology of boreal forest herbs. I. Breeding systems and pollination. Canadian Journal of Botany. 65: 2036-2046.
  6. ^ A record-breaking pollen catapult at Academia.edu
  7. ^ Edwards J, Whitaker D, Klionsky S, Laskowski MJ (2005). "Botany: a record-breaking pollen catapult". Nature 435 (7039): 164. doi:10.1038/435164a. PMID 15889081. 
  8. ^ Hanley, Thomas A.; Cates, Rex G.; Van Horne, Beatrice; McKendrick, Jay D. 1987. Forest stand-age related differences in apparent nutritional quality of forage for deer in southeastern Alaska. In: Provenza, Frederick D.; Flinders, Jerran T.; McArthur, E. Durant, compilers. Proceedings--symposium on plant-herbivore interactions; 1985 August 7–9; Snowbird, UT. Gen. Tech. Rep. INT-222. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Research Station: 9-17.
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Names and Taxonomy

Taxonomy

Synonyms

Chamaepericlymenum canadense (L.) Asch. and Graebn. [305]
  • 305. Weber, William A.; Wittmann, Ronald C. 1996. Colorado flora: eastern slope. 2nd ed. Niwot, CO: University Press of Colorado. 524 p. [27572]

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The scientific name of bunchberry is Cornus canadensis L. (Cornaceae) [95,138,299]. Bunchberry belongs to the Arctocrania subgenus or the dwarf cornels group [70,74,205].
Bunchberry hybridizes with Lapland cornel (C. suecica) to produce Cornus × intermedia (Farr) Calder & Roy L. Taylor [251,261]. Bunchberry also hybridizes with western cordilleran bunchberry (Cornus unalaschkensis) [70]. According to Murrell [205], western cordilleran bunchberry resulted from a past hybridization event in the Pacific Northwest between bunchberry and Lapland cornel.
  • 74. Ferguson, I. K. 1966. The Cornaceae in the southeastern United States. Journal of the Arnold Arboretum. 47: 106-116. [7616]
  • 95. Great Plains Flora Association. 1986. Flora of the Great Plains. Lawrence, KS: University Press of Kansas. 1392 p. [1603]
  • 261. Soper, James H.; Heimburger, Margaret L. 1982. Shrubs of Ontario. Life Sciences Miscellaneous Publications. Toronto, ON: Royal Ontario Museum. 495 p. [12907]
  • 299. Voss, Edward G. 1985. Michigan flora. Part II. Dicots (Saururaceae--Cornaceae). Bulletin 59. Bloomfield Hills, MI: Cranbrook Institute of Science; Ann Arbor, MI: University of Michigan Herbarium. 724 p. [11472]
  • 70. Eyde, Richard H. 1988. Comprehending Cornus: puzzles and progress in the systematics of the dogwoods. Botanical Review. 54(3): 233-351. [6144]
  • 205. Murrell, Zack E. 1994. Dwarf dogwoods: intermediacy and the morphological landscape. Systematic Botany. 19(4): 539-556. [83931]
  • 251. Scoggan, H. J. 1978. The flora of Canada. Part 4: Dicotyledoneae (Dictoyledonceae to Compositae). National Museum of Natural Sciences: Publications in Botany, No. 7(4). Ottawa: National Museums of Canada. 1711 p. [78054]
  • 138. Kartesz, John T. 1999. A synonymized checklist and atlas with biological attributes for the vascular flora of the United States, Canada, and Greenland. 1st ed. In: Kartesz, John T.; Meacham, Christopher A. Synthesis of the North American flora (Windows Version 1.0), [CD-ROM]. Chapel Hill, NC: North Carolina Botanical Garden (Producer). In cooperation with: The Nature Conservancy; U.S. Department of Agriculture, Natural Resources Conservation Service; U.S. Department of the Interior, Fish and Wildlife Service. [36715]

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Common Names

bunchberry

Canadian dwarf cornel

dwarf dogwood

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