Because Picea mariana is a small tree, it has limited commercial value. Frequently it is harvested with P . glauca and used for pulp.
Black spruce ( Picea mariana ) is the provincial tree of Newfoundland.
Morphology: Black spruce grows as a medium- to small-sized tree or as a shrub. Throughout its distribution, mature trees range from 30 to 50 feet (9-15 m) tall and 6 to 10 inches (15-25 cm) in diameter [175,243]. Tree heights in interior Alaska range from 30 to 35 feet (9-11 m) [162], although black spruce often grows in krummholz form or as a <10-foot (3 m) shrub [177,396]. Cold temperatures at high elevations and latitudes force the krummholz and shrub forms [344]. These forms are sometimes described as Picea mariana var. semiprostrata (see Synonyms). Krummholz [25,313] or prostrate [25,179] forms are typical at boreal-arctic ecotones [108]. One hundred- to 200-year-old individuals may be only 10 to 20 feet (3-6 m) tall and 1 to 2 inches (2.5-5 cm) in diameter [129]. In the far north, black spruce's maximum height approximates average snow height [108].
The arrangement of branches and cones promotes easy ignition and torching while protecting seeds. Black spruce trees have a straight bole with little taper and short, compact, drooping branches with upturned ends [113,175,396]. They are short and slender compared to other spruces [113,396]; their form has been described as cigar-shaped [162]. The bole is thin-barked [264,311] and "poorly pruned" [346]: Branches are usually retained after they die [122,383]. Needles are short. Near arctic treeline, needles and cones may be only half the size of those on trees farther south [175]. The cones of black spruce are semiserotinous: they open gradually over time in the absence of fire but open and disperse seeds rapidly when heated by fire [129,152,412]. Cones form dense clusters in the upper part of the tree [2,113]. Generally, they are massed in the upper center of the crown, where they are least likely to sustain fire damage [2]. They are the smallest of the spruce cones [311,346]: only 0.6 to 1.2 inches (1.5-3.2 cm) long [396]. Cones remain on the tree for several years [396]. Seeds support a long, thin wing [396] that is relatively large compared to seed size [395]. Like cones, the seeds are small compared seeds of other spruces [147,242,340], averaging 404,000 seeds/pound [340].
Black spruce has vertical, lateral, and small adventitious roots [65]. The root system tends to be shallow [263], especially in organic soils with a high water table [113] or over permafrost [65]. Most roots grow in the upper 8 inches (20 cm) of organic soil horizons [395], and they are mostly lateral [245]. A review noted that black spruce growing over permafrost may be rooted only in the moss layer [263], but vertical roots sometimes extend into upper permafrost. When this occurs, adventitious roots growing in the organic soil layer help nourish the tree [65].
Stand structure: Structure varies tremendously in black spruce stands, from stringers in open bogs to very open black spruce-lichen woodlands and closed black spruce/feather moss forests. Generally, black spruce density increases with decreasing latitude and is higher on permafrost than nonpermafrost sites. On a site in interior Alaska, black spruce density averaged 2,000 stems/ha on uplands with intermittent permafrost and 11,067 stems/acre on lowlands with permafrost [33]. On the Caribou-Poker Creeks Research Watershed, interior Alaska, black spruce stems are often only 7 feet (2 m) apart. Black spruces rarely exceed 50 (15 m) tall or 10 inches (25 cm) in diameter, and about half are <2 inches (5 cm) in diameter [82].
Most black spruce stands are even-aged and date back to the last fire; however, old stands or stands on poor sites may become uneven-aged [174,197] due to die-off of individual trees [38,174] and subsequent gap succession (review by [47]). In northeastern Ontario, black spruce mortality was not detected in black spruce/feather moss stands <30 years old. Based on a chronosequence of 10 stands ranging from 44 to 82 years old, a self-thinning stage began around postfire year 30 to 40 and lasted about 20 years. Mortality occurred regardless of stand density and did not increase with stand density. It was greatest in drought years [71].
Black spruce generally has a moderate lifespan, although individuals at arctic treeline may be long-lived. Black spruces may live 250 [11,243] to 300 years on favorable lowland sites [11]. In Alberta, maximum recorded ages of black spruce were 200 to 250 years on upper foothills and 270 years in a low foothill bog (review by [245]). In Québec at arctic treeline, where most regeneration is from cloning, researchers dated the oldest stems within a clone at >2,000 years old. The oldest stems within a clone were usually dead, but surrounding live stems were "centuries, if not millennia" old [298].
Black spruce is native to the United States and Canada [210,253,367]. It is primarily a boreal species, although its distribution extends south into the Great Lakes and Northeast regions of the United States. Black spruce's expansion north is hindered by permanently frozen soils. In interior Alaska, young glacial deposits halt its distribution in the southern Brooks Range [255]. In southern Wisconsin, southern Michigan, Pennsylvania, and New Jersey, black spruce is confined to isolated, cold peatlands [172,395]. Climate warming is apparently favoring expansion of black spruce's distribution in the north [35,75] and shrinkage in the south [172].
Countries, states, and provinces [376]:Prescribed fire, without and with logging: Prescription conditions for effective prescribed fires on black spruce sites are more likely to be met in uplands than lowland muskegs, which remain too moist to burn in most years. On the Caribou-Poker Creeks Research Watershed near Fairbanks, the FROSTFIRE research project conducted a prescribed fire in the summer of 1999, burning about 900 acres (365 ha) of mostly black spruce. Fire crowned in most of the black spruce stands, but neither black spruce/sphagnum communities on south slopes and valley bottoms; birch communities; nor quaking aspen communities ignited. Researchers stated that these burn patterns "closely simulated those that occur in natural field conditions" [171]. Soil and forest floor temperatures and nutrient cycling rates increase after fire in black spruce stands. This may result in a warmer, more productive site for 10 to 20 postfire years [380].
On Washington Creek Fire Study and Training Area near Fairbanks, Alaska, Viereck and others [394] found small prescribed fires created a mosaic pattern of different severities that was similar to that created by wildfires. The fires reduced the forest floor by 24% to 62% [394]. For details of this study, see this Research Project Summary: The effects of experimental fires in an Alaskan black spruce/feather moss community.
Experimental prescribed fires were used in the Caribou Range area of the Northwest Territories to relate head fire rate of spread to the Initial Spread Index component of the Canadian Forest Fire Weather Index System for the black spruce-lichen woodland fuel type. The ~160-year-old study forest was near Porter Lake. The canopy was mostly sparsely stocked, stunted black spruce, with some jack pine and paper birch; Easter snow lichen dominated the ground layer. The study design included point-ignition, line-ignition, and wildfire plots. Fires were ignited on 26 June 1982; ground, surface, and crown components were observed during the fires. Head fire rates of spread ranged from 2.0 to 168.6 feet (0.6-51.4 m)/minute, with frontal fire intensities of nearly 33,000 kW/m. Equations presented in the paper help predict of fire behavior in the black spruce-lichen woodland fuel type [10]. See the Research Paper of this study for full details.
After clearcutting black spruce in the Great Lakes states, slash is often broadcast burned to aid natural black spruce regeneration. Burning is generally recommended if there is heavy slash, a feather moss carpet, or abundant tall shrubs, grasses, or sedges [199]. An adequate seed supply is necessary for natural black spruce regeneration, and fuels—including slash, litter, peat, and mosses—need to be sufficiently dry to allow for severe burns [80]. In Minnesota, clearcutting followed by high-severity prescribed fire in early summer produced good black spruce regeneration [375]. Since heavy postfire seed dispersal occurs in postfire years 1 and 2, delaying logging until the second winter after fire may increase natural regeneration of black spruce [149,411]. Black spruce cannot regenerate if cone-bearing branches are removed off site or concentrated in landings [131].
Black spruce may regenerate poorly on sites that are logged without follow-up broadcast burning. In black spruce ecosystems of northeastern Ontario, a chronosequence study comparing stands on 4- to 90-year-old burns to stands that were logged 2 to 126 years prior (and not burned afterward) found that no logged stands had succeeded to black spruce. Quaking aspen and bigtooth aspen had greatest cover on logged sites. Balsam fir cover was higher on logged than on burned sites, although balsam fir was frequent on both sites. Black spruce cover was greatest on burned sites [72].
Tree harvest may be used as a fire surrogate on black spruce sites where prescribed fire is not possible or desired, although black spruce may decline with long-term fire exclusion [45,51]. See Management Considerations for information on this topic.
The seedbed and prefire understory composition can greatly affect black spruce regeneration after logging and/or prescribed burning. Aksamit and Irving [6] studied black spruce regeneration on 27 broadcast-burned clearcuts in northern Minnesota. They found that where sphagnum mosses dominated the ground layer before cutting, black spruce regenerated well regardless of treatment. In fact, adequate regeneration was obtained even without burning. Where feather mosses dominated the ground layer, prescribed burning was necessary for black spruce regeneration [6]. Johnston [199] suggested that to be effective on feather moss sites, prescribed fires are best conducted when 100- and 1,000-hour fuel moistures are <25%. However, burning under these conditions may lead to fire control and mop-up problems, and higher costs. Where speckled alder dominates the understory before logging, natural regeneration of black spruce after broadcast burning is "quite variable". Low-severity fires tend to favor black spruce regeneration, and more severe fires tend to favor tall shrubs [199].
Postfire splitting or checking reduces the salvage value of burned black spruces. In a boreal mixed-conifer forest of central Alberta, order of frequency of splitting (greatest to least) was: balsam fir, black spruce, white spruce, and lodgepole pine. For black spruce trees that split, most split vertically up the bole (53%) but some split in spirals (45%). Thirty-four percent of black spruces did not split. Trees were sampled in severely burned areas of a 1-year-old burn [296].
Salvage logging in burned black spruce communities alters wildlife habitat. Nappi and others [297] review the effects of salvage logging on wildlife biodiversity and provide guidelines for salvage logging on burned boreal sites.
Prescribed burning guidelines are available for managers in the Great Lakes region. Johnston [199] has outlined broadcast burning techniques for lowland black spruce in the Great Lakes states. Humrickhouse [178] presents a prescription for burning cutover black spruce peatlands of Minnesota. McRae [281] provides guidelines for prescribed burning in mixedwood communities in Ontario's Red Clay Belt, where fire spread can be problematic due to discontinuous fuels and many wet areas [281]. See Models for a list of publications providing equations and other tools helpful for predicting fuel loads and fire behavior in different parts of black spruce's range.
Fire Studies available in FEIS:Eastern dwarf mistletoe: Wildfire is the primary factor limiting spread of eastern dwarf mistletoe in unmanaged black spruce stands (review by [13]). Fires of sufficient intensity to kill eastern dwarf mistletoe do not hinder postfire establishment of black spruce [13]. Eastern dwarf mistletoe density tends to increase with stand age [166]. In eastern Minnesota, eastern dwarf mistletoe was not present in black spruce stands <30 years old (Anderson 1949 in [13]). Heinselman [164] stated that "because of the fire exclusion policy and private protection agencies and organizations, we are seeing a vast expansion of dwarf mistletoe in forest areas, particularly on species like black spruce."
Eastern dwarf mistletoe infection on black spruce. Photo taken in Minnesota by Steven Katovich, USDA Forest Service, Bugwood.org. Prescribed fire in black spruce slash to control eastern dwarf mistletoe and improve the seedbed for black spruce regeneration. Photo taken in Minnesota by Fred Baker, Utah State University, Bugwood.org.Prescribed fire helps control eastern dwarf mistletoe in black spruce stands [2]. For such control to be effective, burning must result in 100% black spruce mortality [2,135]. To ensure complete mortality where understories are sparse, live trees can be cut to increase fuels [181].
Eastern spruce budworm: Heinselman [164] speculated that in the Great Lakes area and eastern Canada, outbreaks of eastern spruce budworm may be more frequent than they were historically due to fire exclusion. Outbreaks are most common where old-growth spruce-fir forests are extensive. He wrote that "fire would have frequently curtailed the expansion of these shade-tolerant climax species" (spruces), favoring pine species. A random, but very real fire 'rotation' insured that few stands reached climax", thereby reducing frequency of eastern spruce budworm outbreaks [164].
Eastern spruce budworm outbreaks may increase fuels in black spruce communities [7]. In southern Québec, 7 black spruce stands originated after wildfire occurred shortly after an eastern spruce budworm outbreak that had left many standing dead conifers [141]. In Ontario, a mixed-conifer forest had a 5-year eastern spruce budworm outbreak (1972-1977). Biomass of woody fuels peaked 5 to 8 years after the outbreak (1982-1985). Stand structure changes and increased fuel loads were due to stand mortality, crown breakage, and windthrow. Fire potential was greatest during that time, with fire hazard gradually decreasing as surface fuels—mostly balsam fir debris—decomposed. The infested forest had a sparse eastern white pine-jack pine-white spruce overstory and an understory of budworm-defoliated, dead balsam fir and mostly defoliated, live black spruce [360].
Wildlife: Wildfires in black spruce communities create a mosaic of different forest ages and types, resulting in a mix of habitat types that support a wide variety of wildlife species and guilds. Among the benefits to wildlife [368]:
See IMPORTANCE TO LIVESTOCK AND WILDLIFE for further information on this topic.
Very frequent fires: Black spruce normally seeds in prodigiously following fire, but it may be eliminated from an area if a second fire occurs before black spruce regeneration reaches cone-bearing age [1,263]. Lutz [263] wrote that in Alaska, "repeated fires at intervals shorter than 20 to 30 years (that is, seed-bearing age for black spruce) may result in replacement of the species by treeless communities of sedges, rushes, grasses, and low shrubs". Black spruce regenerated quickly following a 1923 fire in northern Ontario, but no black spruce seedlings were found after a second fire passed through the area in 1929 [283]. In northern British Columbia and southern Yukon, black spruce stands that burned when <25 years old tended to succeed to quaking aspen. For stands that burned when >75 years old, postfire black spruce recruitment tended to be correlated with prefire basal area of black spruce (P=0.02) [201].
Fire occurring within a few decades of an eastern spruce budworm outbreak may also result in poor black spruce recruitment because cone-bearing black spruces do not have sufficient time to recover from defoliation. For example, a 1920 wildfire burned in a black spruce/feather moss habitat type in central Québec. Although the history of eastern spruce budworm outbreaks on the study site was unknown, 3 documented eastern spruce budworm outbreaks occurred nearby between 1930 to 1992. In spring 1995, black spruce cover averaged 14%, but a wildfire that summer killed most black spruces on the study site. In 2011 (postfire year 16), black spruce's cover was only 3.5%. The authors suggested this poor recruitment was due to wildfires in 1920 and 1995, with successive eastern spruce budworm defoliations occurring between the wildfires [84].
Fire and climate change: In western North America, increased fire frequency and/or severity resulting from climate change may cause shifts from black spruce to hardwood types in the southern portion of black spruce's range [75,173,207] and from black spruce woodland to open tundra in the northern portion [30,35,75,315]. Studies in interior Alaska suggest that postfire succession is most likely to shift toward hardwoods when severe fire occurs on moderate- to well-drained sites [204].
Postfire permafrost melting can affect patterns of postfire succession in black spruce communities. In interior Alaska, failure of the permafrost layer to re-form after severe fire may result in type switches from black spruce to hardwood [75,173,207]. See Yoshikawa and others [408] for a discussion and model of fire effects on ground albedo and the active permafrost layer. The model was developed using data from the 1983 Rosie Creek Burn near the Alaska Range [408].
See the FIRE REGIMES of Alaskan black spruce communities synthesis for more information on fire-climate interactions in Alaska.
A model developed for black spruce forests of the Waswanipi region of west-central Québec predicted that compared to wildfire activity from 1975 to 2005, the likelihood of August wildfires would double by 2100. Due to a predicted shift in the fire season, however, the likelihood of May wildfires was predicted to decrease by 20%. The total number of forest fires was predicted to increase slightly in the region [238].
Black spruce may become more abundant in southern boreal regions with climate warming. This trend has been noted in southern Québec. From 1948 to 1995, the total area occupied by black spruce within 16 sphagnum bog-black spruce mosaic bogs in the Bas-St Lawrence region increased from 22.5% to 56.5%. The authors attributed this change to a combination of climate warming, human-engineered drainage affecting portions of all 16 bogs, and wildfires in 11 of the 16 bogs [320].Lutz [264] wrote of wildfire that "this powerful ecological factor has operated as long as the boreal forest has existed". Black spruce ecosystems have mostly lightning-ignited, stand-replacing fires. Most wildfires occur in summer. Most or all vegetation is usually killed or top-killed when black spruce communities burn [264,383]. Black spruce woodlands and forests typically burn with mixed, surface-and-crown fires (for example, [37,103,384,394]). Fires spread easily and uniformly through crowns in black spruce forests [28,264,266,383]. Intermittent or passive crown fires occur in more open communities; these occur in combination [9,124] with lethal surface fires [127] on some sites. Consumption of the organic soil layer (ground fire) typically accompanies both crown and lethal surface fires [206,264,383,404]. Fires in late summer—especially those occurring in dry years or with hot winds—often burn down to mineral soil [383]. In black spruce bogs, which generally have deep layers of soil organic material, ground fires may smolder for weeks, months, or even years [404]. Fire frequencies [383] and sizes vary across black spruce's range. Landscapes may burn in a mosaic pattern [124] or more uniformly [221].
In addition to the discussions that follow, see the Fire Regime Table for information on FIRE REGIMES of vegetation communities in which black spruce may occur. Find further fire regime information for the plant communities in which this species may occur by entering the species name in the FEIS home page under "Find FIRE REGIMES".
Season: Most fires in black spruce ecosystems occur in late spring and summer, with the most severe fires occurring late in the fire season. In boreal ecosystems of interior Alaska and western Canada, the fire season begins in April and extends until September. May and June fires account for about 90% of the acreage burned (~6.9 million acres (2.8 million ha)/year) [190,266]. May, June, and July are typically the most active fire months in Alaska because they have the highest average temperatures and lowest average humidity and precipitation [388]. Severe fire years are correlated with warm, dry air flows [188]. During the Alaskan wildfires in the summer of 2004—an extreme fire year—sites that burned in late July and August had a larger proportion of high-severity fires than sites that burned earlier in the summer (n=90 sites). That summer, interior Alaska had the largest area burned (6.7 million acres (2.7 million ha)) since fire records were started in the 1940s [173].
Type and severity: Black spruce communities experience nearly 100% stand-replacement fires [29,124,262,263,264,368]. Most are rapidly moving crown fires accompanied by surface and ground fires [37,103,185,285,384,394]. Active crown fires usually occur in closed black spruce forests [193,299], although Norum [299] noted that running crown fires are rare in black spruce forests; surface fuels typically carry the fire, with crowning occurring behind the fire front. Fires that occur early in the fire season, while the ground is still frozen, may burn only in the crown. Late-season fires are most likely to burn deeply into organic soil layers [397].
Lethal surface-ground fires may occur in woodlands [141], but such fires are poorly documented [298]. Active crown fires are rare in black spruce woodlands due to the wide spacing of trees, although individual trees and stringers torch [9,220]. Intermittent or passive crown fires occur in lichen woodlands and other open black spruce communities [193,299]; these may occur in combination [9,124] with lethal surface fires [127] on some sites.
Fire moves quickly between strata, traveling up tree boles and transitioning from surface to crown, or vice versa [124]. In forests, crown fires may move within the canopy and never touch the surface [124]. Hollingsworth (2008 cited in [65]) observed wildfires in interior Alaska that burned in crown, surface, and ground layers. She remarked that "after the fire has burned an individual tree it typically drops down and creeps slowly along the ground, depending on how wet the site is" (Hollingsworth 2008 cited in [65]). Low-severity surface fires sometimes occur in black spruce communities [9], but even low-severity fires are usually lethal to black spruce (see Fire Effects).
As applied to fire in black spruce communities, the term "severe" can be misleading [65]. Patterns of postfire succession in black spruce communities are strongly driven by how deeply fires burn into organic soil layers. Therefore, fire severity in black spruce ecosystems is best measured by how much of the organic soil layer was removed (Hollingsworth 2008 cited in [65]). Because the black spruce overstory is usually killed (for example, [298,317]) even when fire severity is low at ground and surface levels [298], fire severity is not a reliable indicator of black spruce mortality [401]. Ryan and Noste [339] stated that in black spruce communities, "the crown fire phase of a wildfire involves primarily the combustion of fine fuels. It devastates the overstory", but may have only slight effects on understory vegetation and organic soil layers [339]. If fire severity was low to moderate on the forest floor, the landscape may show no postfire changes in species composition [65].
Within 4 burned jack pine-black spruce communities of west-central Québec, Jayen and others [185] found fires on most quadrats were stand-replacement, mixed surface and crown fires, although fires apparently did not crown on some quadrats. They assigned fire-impact classes based on aerial surveys in postfire year 6 or 7. Mortality was not differentiated between jack pine and black spruce [185].
Variation in forest fire-impact classes in postfire year 6 or 7 in Québec. Data for high-impact classes were lumped for statistical analyses [185]. Tree condition Fire-impact classDuff, lichen, and/or moss layers in black spruce communities usually support smoldering combustion except when saturated. Video of an experimental fire in a 69-year-old jack pine/black spruce forest in the Northwest Territories showed the continuous flame front was a mix of surface and active crown fire. Rates of spread ranged from 70 to 100 feet (20-30 m)/minute. Tree boles and patches on the forest floor ignited in advance of the flame front, with spot fires from ember rain about 30 feet (10 m) ahead of the flame front. After the flame front passed, residual flaming continued on the forest floor, in downed woody debris, and in tree boles [364].
Ground fires in laurel or other shrublands may result in a type conversion to black spruce. Fires may burn down to mineral soil in extreme fire years, providing a seedbed for black spruce establishment. Once black spruce establishes, the site may become more susceptible to crown fires that perpetuate black spruce. Wein [404] noted areas in Newfoundland that apparently underwent such type conversions. Studies near and within Terra Nova National Park showed that the amount of residual organic matter in the soil was a major driver of postfire succession in this region. Where the residual organic soil layer was >0.8 inch (2 cm) thick in 40- to 100-year-old burns, the site had succeeded to sheep-laurel heathland. Postfire succession was more variable where the residual organic was thinner; such sites succeeded to either sheep-laurel savanna or black spruce forest. The authors suggested that on sites with shallow residual organic matter, an abundance of sprouting shrub species before fire may lead to dominance of sprouting shrubs after fire, while black spruce may dominate sites that had few shrubs before fire [347].
Because of irregular terrain and differences in substrate moisture, fire severity may vary greatly within black spruce communities. A study in central Saskatchewan found fire severity differed at microsite but not landscape levels. The landscape was comprised of closed-canopy black spruce/Schreber's moss-dark sphagnum stands on permafrost bogs and open black spruce/bog Labrador tea/dark sphagnum stands on nonpermafrost bogs. It burned in a March 1999 wildfire. In June 1999, 4 peat cores—2 from each stand type—were collected to determine fire severities. Based on ash concentrations, the researchers found high within-site variations in the amount of burned peat across the landscape (P=0.01). Areas of highly combusted peat often lay within 20 inches (50 cm) of lightly scorched or unburned peat. The authors were unable to account for these differences in fire severity. There were no significant differences in fire severity either across sites or between permafrost and nonpermafrost sites [374].
A study in black spruce and jack pine-black spruce stands of central Saskatchewan showed fire severity was greatest on sites with relatively low duff moisture. Comparing smoldering duff consumption on 2 sites with similar duff characteristics, duff consumption was greater during the Waskesiu Lake Wildfire of July 1998 than during the Bittern Creek Wildfire of June 1996. Both fires crowned, but the ground fire component was more severe on the Waskesiu Lake site. Based on measurements from adjacent unburned sites, this was likely because percent duff moisture was less on the Waskesiu Lake site than on the Bittern Creek site (5%-8% vs. 12%-16%, respectively). Both fires burned down to mineral soil in patches, but the Waskesiu Lake Burn had a wider range of sizes for mineral-soil patches, and average mineral-soil patch size was larger (P<0.001 for all variables). The study provided some additional information on ground fuels that pertains to fire severity: For unburned sites near both burns, low-slope black spruce stands on glaciofluvial deposits had significantly deeper duff layers (4.06 inches (10.3 cm)) compared to upper-slope unburned jack pine-black spruce stands (2.72 inches (6.9 cm), P<0.05). Bulk density of the duff was not significantly different between black spruce and jack pine-black spruce stands. Duff was drier beneath than between trees, probably due to interception of precipitation by tree crowns [285].
Frequency: Black spruce types in general have stand-replacement fires about every 75 years (review by [85]). Fire-return intervals range from 30 to 100 years in black spruce ecosystems [165,233]. Heinselman [167] calculated mean fire-rotation intervals of 100 years for closed black spruce forests and 130 years for open black spruce-lichen woodlands across Alaska. Fire-return intervals tend to increase from west to east [168]. Fire-return intervals increase eastward across boreal Canada, from the relatively dry continental boreal forests toward the Atlantic seaboard. The longest fire-free intervals for spruce stands probably occur in southern Labrador, where the fire-rotation interval for black spruce forests is estimated at 500 years [128]. For a summary of fire-return intervals and rotations across black spruce's distribution, see Table 2 in FEIS's FIRE REGIMES of Alaskan black spruce communities synthesis.
Fire-return intervals lengthen toward arctic treeline. Open black spruce-lichen woodlands in the Northwest Territories and northern Québec have fire-return intervals of ≥100 years [54,271,319]. Some black spruce stands in northern Québec have been aged at >2,000 years old [298]. On a site near Inukjuak, fire-return intervals ranged from 100 to 1,800 years [227].
Upland taiga burns more frequently than lowland taiga. Black spruce stands on muskegs generally experience longer fire-free intervals than nearby upland stands, and they often become uneven-aged with succession [395]. East of Great Slave Lake, black spruce/dark sphagnum peatlands burn about half as often as drier, upland black spruce communities. In observations of >30 burns in the low peatlands, burn patterns were patchy, with peat burned away only around some trees [184]. Johnson [189] reported MRFIs (mean fire-return intervals) of 70 to 100 years for black spruce communities in this region of the Northwest Territories. In the Boundary Waters Canoe Area, black spruce tends to occupy large, upland ridges distant from lakes; these areas burn more frequently than valleys, lower slopes, and lacustrine areas, which are typically occupied by pines and white spruce. Fire-rotation intervals range from 50 to 100 years for black spruce forests in the area, with fires sometimes skirting black spruce peatlands [166]. In southeastern Labrador, fire frequency was less on an interior plateau that was broken up by "extensive peatlands and numerous lakes" than on watersheds with more variable topography and few peatlands [127].
Black spruce peatlands may burn only in dry years. Once ignited, ground fires in peatlands may smolder for weeks, months, or even years. Fire frequencies are highly variable in peatlands and bogs. Small peatlands may burn at the same frequencies as the surrounding plant communities, but generally at lower severity and in a patchy pattern [404].
Based on reviews, Frost [136] mapped black spruce ecosystems of the Great Lakes states and Maine with 26- to 100-year fire-return intervals.
In west-central Alberta, a history of stand-level, crowning wildfire followed by several successive mixed-severity wildfires was documented for 6 mixed-conifer forests dominated by lodgepole pine, white spruce, and black spruce. Crown fires had occurred 120 to 300 years prior. The stand-replacement wildfires were followed by low- to moderate-severity wildfires that left live, fire-scarred lodgepole pine in each of the 6 forests. Return intervals of the low- and moderate-severity wildfires averaged <80 years and ranged from 29 to 167 years [16].
Pattern and size: Patchy fires are common in black spruce communities, with patches burned down to mineral soil intermixed with unburned patches and patches where the soil organic layer was partially burned [124,184]. Upland black spruce communities tend to burn more uniformly than lowland black spruce peatlands. Sphagnum mosses can absorb and sequester water up to about 20 times their own dry mass [325]. This likely explains why black spruce peatlands with >7 feet (2 m) of accumulated sphagnum dry slowly and rarely burn [221].
A burned black spruce/sphagnum stand in interior Alaska. The brown patches on the forest floor are live, scorched sphagnum. The brown sphagnum patches held so much water that they did not ignite. U.S. Forest ServiceIn burned jack pine/black spruce stands of southeastern Manitoba, most unburned areas were large bogs or fens. Time since fire averaged 70 years on densely treed wetlands—some of which were skirted by previous fires—and >120 years on wetlands with shallow water tables. At the landscape level, this resulted in an uneven-aged forest. Large wildfires accounted for the "vast majority" of area burned from 1955 to 1983. Large fires ranged from 500 to 200,000 acres (200-90,000 ha), with a median of 25,390 acres (10,155 ha). On 6 large burns, residual unburned islands were rare, occurring mostly near burn perimeters and in wetlands. [106].
Fire size varies greatly in black spruce communities (review by [85]). Most fires are small [127]. "Ecologically significant" fires are infrequent, but they can be large (>400 mile² (1,000 km²)) [127]. A few large fires (≥123,500 acres (50,000 ha)) [304,383] occurring in extreme fire years account for most acreage burned (for example, [106,127,383,395]). Burns of 500,000 acres (200, 000 ha) are common [304,333]; in some years, millions of acres may burn [304]. On sites across Alaska, 6 years accounted for 63% of total area burned from 1940 to 1977 [383]. Over 81 years (1863-1944) in the Mackenzie Valley, Northwest Territories, 42% of all fires occurred in 5 dry years, and in the northern portion of the valley, 60% of all fires occurred in 4 dry years. The fire-rotation interval was 80 to 90 years in black spruce communities [333].
Regional studies: Regional trends in fire ignition, season, type and severity, pattern, and size are discussed below. Alaska: Most wildfires in Alaskan black spruce communities are ignited by summer lightning. Documented mean fire-return intervals since the 1700s range from about 40 to 200 years [95,213]. Wet and stringer black spruce communities generally have longer fire-return intervals than mesic communities [85,395]. Fires typically crown, with accompanying surface and ground fire [82,206,264,383,404]. Most fires are small, but a few large fires account for most acreage burned [32,323]. Except near settlements, few Alaskan black spruce communities have been subject to fire exclusion [69]. See the FIRE REGIMES of Alaskan black spruce communities synthesis for detailed information and documentation of FIRE REGIMES in this area.Great Lakes: Fires are more frequent in pine-black spruce forests than in black spruce bogs. In Michigan, fire-return intervals of jack pine-black spruce forests are estimated at 50 to 100 years, with a mean of 80 years [132]. Fire-return intervals for jack pine-black spruce forests in the Boundary Waters Canoe Area range from about 50 to 70 years [251]. In pine-spruce forests of the Boundary Waters Canoe Area, Heinselman [164] documented "major fires" from at least 1600 to 1920 . Some areas reburned in 10 years, while others had not burned for 200 to 300 years [164,166]. The longest fire-rotation interval was around 360 years. From the 1920s to the 1970s, only "limited areas of virgin forest ... burned, due to effective fire control" [164]. Fire exclusion in this region may lead to very long fire-return intervals: In the 1990s, the fire-rotation interval for Boundary Waters Canoe Area was estimated at >1,000 years [134].
Because they are so wet, black spruce peatlands do not burn except in extreme fire years. For black spruce swamps in the Great Lakes states, LeBarron [243] noted that "during drought periods when water levels are low they can burn very fiercely, and when they do spruce timber is killed almost entirely". In Itasca State Park, Minnesota, Heinselman [168] found that fire sometimes skirted black spruce and black spruce-tamarack bogs on Laurentian uplands, glacial moraines, and outwashes. Fire-return intervals of upland areas were 20 to 40 years; he was unable to determine how often the bogs burned [168].
Fires typically crown in pine-black spruce and black spruce muskegs of the Great Lakes region [3,229]. In northeastern Minnesota, a mid-July wildfire burned a jack pine-black spruce site with a mixed crown, surface, and ground fire. The ground fire was described as "very hot", burning all litter, much of the duff, and exposing mineral soil on some microsites [3].
On the Pictured Rocks National Lakeshore, Michigan, black spruce is a minor species in mixedwood forests. The historical MFRI for the area is 21.8 years [257], which is too frequent to support black spruce stands (see Cone and seed production).
Northeast: Little information was available on FIRE REGIMES of black spruce communities in this region as of 2014, but since black spruce communities are wet, it is likely that fires are infrequent. In northwestern Maine, black spruce forests have an approximate 145-year fire-return interval. Between 20 to 200 acres (10-100 ha) usually burn [228]. Fires can be large in extreme fire years. In southwestern Maine, a 1947 wildfire burned 130,000 acres (53,000 ha) of forestland, about 580 acres (230 ha) of which was balsam fir with black spruce and/or red spruce [31]. Fires on deep, coarse glacial outwash can be intense, and black spruce communities on glacial outwash tend to remain in the heath-lichen stage of postfire succession longer than is typical for black spruce types of Maine [228].
FIRE REGIMES of black spruce communities in Maine are likely similar to those of southern Québec [43,74]. See the Eastern Canada section for information on FIRE REGIMES of black spruce communities in Québec.
The red maple-black spruce-highbush cranberry vegetation association of New Jersey rarely burns. It is classified in Fuel Model 0: the ground is saturated and the probability of the vegetation carrying fire is very low [321].
Canada: Throughout much of boreal Canada, spruce stands burn at 50- to 150-year intervals [167]. Across boreal Canada, large fires were least common in the Hudson Plains (0.24 fire/year/4,000 mile² (10,000 km²)) and most common in the Boreal Shield West (Central Plains) region (1.12 fires/year/4,000 mile²). Mean size of fires in the Taiga Plains (west-central) region was significantly larger (31,501 acres (12,748 ha)) than in the Boreal Plains (western interior) (15,458 acres 6,183 ha)) and Boreal Shield East (eastern interior) (12,955 acres (5,182 ha)) regions (P<0.001). Generally, large fires in communities with highly variable substrate moistures, such as black spruce, had proportionately more unburned islands within fire perimeters. Fire seasons arrived later in northern than southern regions. There was a shift toward more spring fires near human settlements [68].
Western Canada: This region has highly variable fire frequencies, types, and patterns. Fire-return intervals range from <20 [73] to >300 [54,356] years. Along the Dempster Highway in central Yukon, fire-return intervals in black spruce woodlands or adjacent shrub tundra communities ranged from 33 to over 300 years. The longest interval detected was 343 years, for a black spruce/carex sedge/fireweed stand [356]. Modeling indicates that black spruce-lichen woodlands of western Canada have a regime of ≥18% crown fire, 8% to 17% intermittent crown fire, and ≤7% surface fire. Intermittent crown fires are defined as those with discontinuous torching. They represent the transition zone between severe surface and active crowning fires, with flames extending from the forest floor to above tree crowns [9].
Studies in the Northwest Territories illustrate variations in FIRE REGIMES in black spruce ecosystems of western Canada. The fire season runs from about mid-June to mid-August. In the upper Mackenzie Valley and adjacent uplands, fires were considerably more frequent in jack pine stands (FRI range: 40-60 years) than in black spruce stands (100-200 years) [335]. Time since fire for 19 black spruce/bog blueberry woodlands near Inuvik ranged from 3 to 300 years; most stands were <100 years old [54].
Fire history studies of Nahanni National Park and the Mackenzie Bison Sanctuary, Northwest Territories, found the 2 areas had similar fire-return intervals and fuel loads despite important differences in weather, topography, and fire sizes. Both sites have open black spruce-white spruce boreal forests containing quaking aspen and paper birch. Climate at the Mackenzie Bison Sanctuary is strongly influenced by nearby Great Slave Lake and is harsher than that of Nahanni National Park. Mean fire-return interval of Nahanni National Park was 21.7 years from 1813 to 1974; for the Mackenzie Bison Sanctuary, it was 23.3 years from 1771 to 1977. Nahanni National Park averaged 0.084 large fire/year/200,000 acres (100,000 ha) from 1959 to 1999, while the Mackenzie Bison Sanctuary averaged 0.056 large fire/year/200,000 acres. Large fires were >500 acres (200 ha)). Nahannia National Park had more small fires, while the Mackenzie Bison Sanctuary had fewer but larger fires; this tended to even out the area burned. The authors speculated that steeper topography in Nahanni National Park may have increased fire frequency by increasing fuel continuity. They cautioned that these are conservative estimates, and fires may be more frequent than their results indicate [60].
The Caribou Range area of the Northwest Territories experiences short to moderate fire-return intervals, with discontinuous, infrequent fires in wet areas. From the mid-1970s to the early 1990s, this 1.38 million-acre (5.60 million ha) area averaged 34 fires/year; most were stand-replacement fires. Mean burn size was 226,200 acres (91,533 ha) [126]. From 1966 to 1975, Johnson and Rowe [191] documented 398 fires in the Caribou Range area, 89% of which were lightning-ignited. A total of 1.7 million acres (0.7 million ha) burned within those 10 years, with "large variation" in fire size across years. Mean fire-return intervals ranged from 55.5 to 101.1 years for 4 lacustrine sites. Some sites had not burned for about 150 years [192]. In black spruce-lichen communities of the area, fires did not always carry from open lichen patches into black spruce stands; these discontinuous fires remained on the surface and their severity was low [10].
On sandy soils in northeastern Alberta and northern Saskatchewan, fire-return intervals averaged 38 years (range: 28-54 years) in both upland jack pine-black spruce/bog Labrador tea/green reindeer lichen forests and more open, lowland jack pine-black spruce/bog Labrador tea/green reindeer lichen forests. Lowlands with no fire for ≥90 years showed a shift in groundlayer vegetation from green reindeer lichen to globose haircap moss, with an attendant increase in black spruce [73]. In Wood Buffalo National Park, northern Alberta, the fire-rotation interval for black spruce forests was 78 years: significantly longer than for jack pine or quaking aspen forests. Fire-rotation intervals increased significantly as distance from waterbreaks increased (P=0.05 for all variables) [233].
Eastern Canada: Fires are common and ecologically important in both spruce and mixedwood ecosystems of eastern Canada. Alexander and Euler [8] stated that the eastern boreal mixedwood forest "is a fire-dependent ecosystem that would lose its character, vigor, and faunal and floral diversity in the absence of fire". In boreal western Québec, 71% of the area burned from 1945 to 1998 was due to lightning, but most fires were small and started by humans (62% human ignition vs. 38% lightning) [249]. Generally, wildfires occur only during intervals of low precipitation or low relative humidity (<60%), which allows the litter layer to dry. Ignition and fire spread are most likely when high-atmospheric-pressure systems dominate for at least 3 days, during which rainfall is <1.5 mm. These conditions usually occur from late spring through early summer, after snowmelt but before deciduous leaves have fully flushed out (review by [70]. Because there are fewer flammable conifers in mixedwood stands, ignition is more difficult than in conifer stands [92].
Black spruce lowlands of eastern Canada may be too wet to burn in most years and therefore, have longer fire-return intervals than upland vegetation. In Quetico Parks, Ontario, Heinselman [168] found that fire sometimes skirted black spruce and black spruce-tamarack bogs on Laurentian uplands, glacial moraines, or outwashes. Fire-return intervals of upland areas were 20 to 40 years; he was unable to determine how often the black spruce bogs burned [168].
In Québec, black spruce tends to dominate in early postfire succession in mixed-conifer communities and in late postfire succession in mixedwood communities. In mixedwoods, short fire-return intervals favor hardwoods over black spruce and other conifers because the hardwood species sprout soon after fire, before conifers are old enough produce seed [8]. In southern and central Québec, where black spruce cooccurs with pines, aspens, and birches, black spruce is most common in areas that have moderate to long fire-return intervals [94], ranging from about 70 to 200 years. Balsam fir dominates areas with very long fire-return intervals. Day and Harvey [92] estimated fire-return intervals of approximately 75 years (SD 50) for boreal mixedwoods of southeastern Canada. Black spruces older than 150 to 200 years are scarce in mixedwoods. Lowland mixedwoods [8]—where black spruce is most prevalent—burn less often than upland mixedwoods [8]. In study in boreal eastern Québec, most of the landscape was occupied by mixedwood stands >150 old. Based on field data and modeling, black spruce was associated with sites that had relatively frequent fire (MFRI=164 years), while balsam fir was associated with sites that had infrequent fire (MFRI=722 years, P<0.0001 for both variables) [87]. For the Waswanipi region of central Québec, the fire-rotation interval between the 1940s to the 2000s was estimated at 132 to 153 years [239]. Near James Bay, fire-rotation intervals were estimated at 495 years for black spruce and 3,142 years for white spruce. Occurrence of black spruce was negatively correlated with time since fire (R = -0.75), while occurrence of white spruce was positively correlated with time since fire (R = 0.89) [312]. In boreal mixedwood lowlands of northeastern Québec, fire-return intervals are long enough to allow paludification to occur (see Successional Status). In the Lake Matagami Lowland region, time since fire for black spruce stands ranged from 160 to 1,585 years [20].
Studies in northern Québec show very long fire-return intervals at the boreal-arctic treeline and mostly vegetative regeneration. Black spruce occurred in scattered stands on sites that burned <600 years prior, while reindeer lichen tundra more was common on sites that had not burned for >1,500 years. This slow rate of succession suggests that black spruce communities rarely burn in this region (review by [313]). Tree ring data showed a black spruce-lichen woodland near arctic tree line had not burned for 850 to 900 years [318]. At the present arctic treeline near Chibougamau, fire frequency is low: estimated at 0.04 fire/year in the 20th century. Black spruce grows mostly as layering krummholz, with some stands originating >2,000 years prior [298]. At the northern treeline-tundra interface near Inukjuak, time since fire ranged from 100 to 1,800 years. Black spruces were regenerating solely by layering [227].
A study in a black spruce-lichen woodland in the Boniface River area of northern Québec found a MFRI of around 1,000 years. Black spruce had apparently cloned for 1,500 to 1,700 years before a wildfire deforested the area [25] in the mid-1500s. Carbon-14 dating showed the area had at least 3 fires in 2,500 years: around 350 BC, 10 BC, and in 1567 AD [27]. Black spruce did not regenerate after the 1567 fire; the prefire black spruce clones were likely unable to produce cones due to cold temperatures (see Cone and seed production). Presently, the postfire community is a treeless tundra community dominated by reindeer and other lichens. The authors attributed the type shift from black spruce woodland to lichen tundra to climate warming in the region [25,26,27].
A jack pine-black spruce community in the North Shore area of Québec had a MFRI of 75 years, averaged over the last 1,000 years. Intervals were frequent enough to maintain jack pine dominance and black spruce codominance; longer fire-return intervals would likely shift dominance to black spruce [316].
Spruce-fir and mixedwood ecosystems of eastern Canada often experience mosaic fires [8]. Boreal mixedwood landscapes are usually comprised of small to large patches of different-aged stands that originated after fire. Although black spruce density generally increases with time since fire in mixedwoods [94], closed-canopy black spruce stands rarely have enough time to develop before the next fire [92].
A study of mixed-conifer forests in south-central Québec found a pattern of large fires with long rotations. Over 2,000 miles² (5,000 km²), most of the landscape (55%) was old-growth black spruce-jack pine-paper birch/feather moss forest. Fire size averaged 25,282 acres (10,113 ha), with most detectable fires burning more than 20,000 acres (10,000 ha) (n=176 burns). The authors thought that more small fires occurred than had been detected. Mean fire-rotation interval averaged 247 years from 1734 to 2009 [38].
In a mixedwood forest in Timiskaming, southwestern Québec, no large fires were noted from 1950 to 2000, and <12,000 acres (5,000 ha) of the 1,000-mile² (2,500 km²) study area burned. Mean time since fire averaged 136 years (SD 60); approximately 52% of stands were older than 100 years. Balsam fir and yellow birch were the most common trees throughout the area, but black spruce was most common on xeric sites [150].
A dendrochronological study suggested that fire size and severity are important factors controlling the transition from boreal spruce-fir forests to southern mixedwood forests. Across 315 sites in northwestern Québec, fire frequency decreased around 1850, at the end of the Little Ice Age, compared to the previous 80 years. Fire frequency increased during the settlement period (1910-1920). From 1920 to 1945, there was a trend of large fires in southern mixedwood ecosystems; however, there were few fires in northern boreal spruce-fir ecosystems. Time since fire was not significantly different between the 2 ecosystems, although stands on xeric and surficial-deposit sites were younger than those on moist sites. After 1945, there were more fires in the south than the north, and fires were smaller in the south. Proportions of unburned land were similar for the ecosystems. Among all stands examined, black spruce dominated 25% of mixedwood and 90% of spruce-fir ecosystems, with 69% and 53% frequency, respectively. From 1953 through 1996, MFRIs were 90 years for the mixedwood and 85 years for the spruce-fir ecosystems, respectively; differences were not significant. There were no significant differences in fire weather parameters (for example, relative humidity) between the 2 ecosystems, although the mixedwoods had more lightning strikes [48].
Climate change effects on Fire-return intervals in boreal black spruce communities have lengthened and shortened with long-term patterns of climate cooling and warming, respectively. Sediment-core studies in southwestern Québec found that charcoal concentrations—a surrogate for fire frequency—increased greatly after the mid-Holocene. Analyses of cores from Lac á la Pessiére found MFRIs averaged 64 years (SE 55) from 3,300 to 1,300 BP and 439 years (SE 100) from 1,300 BP to present. Charcoal concentrations increased about 1,000 years earlier in northern boreal spruce-fir forests than in southern boreal mixedwood forests. The authors suggested climate triggered increases in fire frequencies, with cool, dry Pacific air masses creating drier conditions that were conductive to fire ignition and spread. Present-day old growth in the area is dominated by balsam fir and/or black spruce on mesic sites and black spruce on xeric sites [70].
The current trend of increasing fire frequencies and sizes in black spruce ecosystems is well documented (for example, [171,214,368]). A review reported that in the 2000s, 1.90 million acres (767,000 ha)/year of Alaska's boreal forest burned. This was a 50% increase from the 1940s to the 1990s. The area burned in late-season wildfires increased in the 1990s and 2000s. These late-season fires generally resulted in deeper burning of organic soil layers than had occurred previously. Poorly drained, black spruce-sphagnum sites did not experience the deep-burning ground fires [214]. See FIRE REGIMES of Alaskan black spruce communities for further information on this topic.
On the Kenai Peninsula of Alaska, spruce bark beetles were a greater disturbance in black spruce forests than fire. However, the authors suggested that interactions of spruce bark beetle attacks and climate warming may lead to increased fire frequencies (abstract [41]).
Warming climate may not result in increased fire frequencies in parts of black spruce's range in the eastern United States and Canada. A review reported that fire frequency in boreal forests of western Québec has decreased since the end of Little Ice Age (~1850 AD) despite warmer temperatures. This has been attributed to influences of warm, moist air flows during the fire season. Based on surveys of burned sites across Canada, Flannigan and others [119] asserted that "Increased temperature alone does not necessarily translate into greater fire disturbance".
Studies at the arctic treeline in northern Québec showed that from around 300 to 1500 AD, relatively warm temperatures favored black spruce. Size of the black spruce ecosystem contracted during the Little Ice Age (1600s-1850). With warming temperatures in the 19th and 20th centuries, the extent of black spruce ecosystems has shrunk yet again, while open peatlands have expanded [315].
Treeline black spruce communities may recover very slowly after fire, because most regeneration at arctic treeline is from cloning rather than postfire seedling establishment. Based on current, slow rates of black spruce regeneration and postfire recovery at their study site, Payette and others [298] predicted that despite warming temperatures, eastern black spruce-lichen woodlands will not expand into tundra ecosystems of northeastern Canada.
Sustained seedfall over several postfire years helps ensure black spruce's establishment during favorable years [366]. Although large amounts of seed disperse during postfire year 1, small amounts of seed rain continue for several more years. For example, seedfall continued for 8 years following fire in a 70-year-old black spruce stand in interior Alaska [390]. See Regeneration Processes for detailed discussions of black spruce's postfire seed dispersal, germination, and establishment.
Plant response to fire: After fire, black spruce establishes from crown-stored seed that disperses from its semiserotinous cones [2,263,383,388,415]. Large quantities of seeds are released soon after fire [2,113,124,263,319,385,406]. In fact, striking recently fire-killed black spruce trees with an axe causes seed rain [243]. Sixty days after a fire in Newfoundland, black spruce seed rain averaged 1,500,000 seeds/acre. Before the upland site burned, the black spruce stand averaged 40 feet (12 m) tall and 188 feet² (17 m²) in basal area [406]. After severe fire in central Alaska, a stand that averaged 909 black spruce snags/ha had an estimated seed rain of 8,200,000 black spruce seeds/ha. Based on the 41% germination rate of a seed lot collected from the burn (n=6,400 seeds), there were approximately 3,400,000 viable seeds/ha [389].
Seed sources are usually on-site trees killed by a recent fire [262,375], supplemented by unburned islands of trees [263]. Seed may also blow in from off-site parents [262,263,290]. In wet lowlands, unburned stringers of black spruce provide off-site seed that disperses onto adjacent burned areas [263]. Some black spruce established from off-site, wind-blown seed after the 1950 Porcupine Wildfire in interior Alaska, which burned 1.7 million acres (0.7 million ha). By postfire year 30, saplings were 7 to 13 feet (2-4 m) tall, and a few trees were producing cones [123,125]. DBH averaged 1.7 inches (4.4 cm) [125]. In Alberta, Eberhart and Woodard [105] found moderate-sized fires left more residual unburned areas than small or large fires.
Black spruce seed production is poor at the taiga-tundra ecotone so generally, little or no seed is available for postfire regeneration. Where seed production is sparse, short-term climatic changes over 1 to 10 years can exhaust the seed population before a fire or prevent seed germination after a fire. Black spruce stands did not regenerate after a fire near arctic treeline in the Northwest Territories [54,55]. At arctic treeline in northern Québec, fires can eliminate or severely reduce black spruce and cause a shift toward arctic tundra. Here, black spruce seedlings are only occasionally found after fire: They are usually in depressions at the edge of burned areas, where cones of nearby living trees contain viable seeds [319].
A type shift from black spruce-lichen woodland to treeless tundra occurred after wildfires at arctic treeline in the Northwest Territories [54] and northern Québec [25,26,27]. A growth-chamber experiment using seed collected in the Northwest Territories found black spruce germination stopped at temperatures below 49 °F (15 °C) [55], suggesting that germination of black spruce is unlikely after fire near arctic treelines.
Following fire, black spruce establishes best on lowland sites with partially burned moist peat or on upland sites where severe fire exposes mineral soil [243,414]. Most fires do not consume the entire forest floor; mosaic fires result in small patches of exposed mineral soil intermixed within larger areas of partially consumed organic material [124], ensuring a variety of potential seedbeds. However, late summer fires sometimes consume the entire organic soil layer and expose extensive areas of mineral soil [390]. Unburned or partially burned sphagnum mosses also provide good seedbeds, but unburned or partially burned feather mosses are generally less favorable [6]. A fire in southern Ontario did not wholly consume fire mosses and hence, did not foster black spruce establishment. However, rotting logs under the feather mosses were often exposed and provided excellent seedbeds [276]. See Seedbeds for further information.
Most black spruce seedling establishment occurs within 10 postfire years [206]. In Québec, most new seedlings established within 3 postfire years [138]. In interior Alaska, Foote [124] found an average of 17,954 black spruce seedlings/acre on black spruce sites that had burned 1 to 5 years prior. In 50-year-old stands, black spruce had self-thinned to 2,595 stems/acre; trees in these stands averaged 2.1 inches (5.4 cm) D.B.H. and were 16.4 to 23 feet (5-7 m) tall [124]. After Alaska's Wickersham Dome Wildfire, most seedling establishment occurred within 3 to 5 postfire years. Even on sites where fire severity was low and some surviving adults produced new cones after fire, most establishment apparently came from fire-opened cones [384]. Johnstone [206] suggested that declines in seedbed quality, such as litter accumulation or sphagnum development, may limit black spruce establishment as postfire succession proceeds. Permanent plots in boreal Alaska and Yukon showed black spruce seedling establishment occurred within 10 postfire years, with most seedlings establishing in postfire years 3 to 7 (review by [151]).
Most studies found postfire density of black spruce seedlings was proportional to prefire basal density of mature stands (for example, [146,147,201]). Dense, pure black spruce stands commonly establish in the first few decades after fire in interior Alaska [396]. On 30-year-old burns, Lutz [263] reported mean black spruce density at 5,000 one-inch- (2.5 cm) diameter stems/acre. In 100-year-old burns, density of stems ≥5-inch (13 cm) diameter ranged from 2,000 to 3,000 stems/acre.
Black spruce density generally drops after the first few postfire decades due to self-thinning. In the Northwest Territories, Rowe and others [335] found mortality of black spruce increased 4-fold from postfire year 80 to postfire year 100.
Fire-return intervals and depth of burn into the organic soil layer (see Seedbeds) affect postfire recruitment of black spruce. Postfire seedling establishment of black spruce is reduced or curtailed when fire-return intervals are so short that few or no trees reach cone-bearing age. Removal of all or most of the soil organic layer reduces black spruce recruitment when hardwood regeneration interferes with black spruce establishment or when the permafrost layer thins after losing the insulating organic soil layers. Sites may experience permafrost thinning where the organic soil layer is <4 inches (10 cm) thick (review by [265]).
A deep permafrost layer helps protect a site from severe ground fire. After fire, there may be fewer changes in species composition on sites with a deep permafrost layer. Studies of burns near the headwaters of the Kobuk River found permafrost on the coldest, wettest sites usually did not thaw deeply after fire. Cold sites included concave positions, low slopes, and north-facing midslopes. Permafrost on warmer or dry sites thawed deeply in some cases, but not in others. Warmer sites with permafrost included convex positions, crests, shoulders, and east-, west-, and south-facing midslopes. Dry sites were on convex positions and upper slopes, usually with sand and gravel at shallow depths. These lacked permafrost regardless of time since fire. Sites where permafrost failed to thaw after fire showed only weak changes in postfire vegetation, while sites where permafrost thawed deeply showed greater changes in postfire plant community composition. Paper birch and quaking aspen were most abundant on dry sites, while black spruce was present on all sites. Feather mosses and sphagnum were most abundant on sites where permafrost remained after fire, while lichens and haircap mosses were most abundant on thawed, dry sites. The burns resulted from fires dating from 1959 to 1991 (≤37 years prior) [363].
See Regeneration Processes for further information, including information on prefire seed production and postfire seed dispersal, germination, establishment, and growth. Successional Status discusses general patterns of postfire succession in black spruce communities. Examples of black spruce response to fire by region follow.
Alaska: In Alaskan studies, black spruce generally showed best establishment on mineral soils or soil where most of the organic layer was burned off. If dominant before fire, it usually regained dominance within 10 postfire years. On 4 wildfire-burned sites in interior Alaska and central Yukon, germination of hand-sown black spruce seed was significantly greater on high-severity plots with exposed mineral soil than on low-severity plots with organic soil (P<0.01). Growth of transplanted seedlings was faster on high-severity than on low-severity plots (P<0.01). Fire severity had less effect on seedling survivorship, although survivorship was about 15% greater on high-severity than on low-severity plots (P=0.07). The prefire communities were mixes of black spruce, white spruce, and lodgepole pine; the study sites were in early postfire succession (postfire year 1 or 2). In general, high-severity plots had greater total tree density than low-severity plots [206].
Across burned black spruce-reindeer lichen woodlands of the central Brooks Range, most postfire seedling establishment of black spruce occurred in postfire years 10 to 35 (n=346 plots). Black spruce height growth averaged 1.3 inches (3.3 cm)/year, which was slightly more than that of white spruce (1.0 inches (2.6 cm)/year) [79].
Foote [124] found that on mesic black spruce sites in the Tanana River valley, black spruce seedlings were about twice as numerous as quaking aspen seedlings and sprouts and about 50 times as numerous as paper birch seedlings and sprouts in postfire years 1 to 5. Quaking aspen and paper birch seedlings and sprouts grew faster than black spruce seedlings until after about postfire year 30, but black spruce was more abundant in all successional stages. Black spruce's density peaked in the moss-herb stage [124].
Table 2. Mean black spruce density and frequency in the Tanana River valley, Alaska (SD) [124] Postfire years Successional stage Age class Density (stems/ha) Frequency (%) <1 newly burned seedlings 0 0 saplings 0 0 trees 0 0 1-5 moss-herb seedlings 17,954 (14,972) 58 (35) saplings 13 (23) 23 (40) trees 48 (154) 23 (39) 6-30 tall shrub-sapling seedlings 12,881 (29,251) 40 (40) saplings 4 (7) 8 (8) trees 2 (5) 5 (22) 31-55 dense tree seedlings 240 (534) 77 (33) saplings 1 (1) 83 (32) trees 358 (736) 17 (33) 56-90 mixed hardwood-spruce seedlings 10 (19) 750 (1,548) saplings 417 (718) 92 (9) trees 1,550 (1,183) 85 (20) 91-200+ spruce seedlings 4,688 (4,942) 40 (37) saplings 225 (300) 52 (55) trees 1,680 (473) 99 (2)Three years after an experimental prescribed fire on black spruce/feather moss sites on the Washington Creek Fire Ecology Experimental Area, naturally dispersed and artificially sown black spruce seeds established only where fire had removed part or all of the organic matter. No seedlings were found on unburned, scorched, or charred feather moss substrates. In general, exposed mineral soils provided the best seedbeds. None of the black spruce seedlings that established in areas with some organic soil layer remaining survived past postfire year 3. However, on sites where mineral soil was exposed, seedling frequency of black spruce was 35% in postfire year 1 and 81% in postfire year 3; this was a result of continuing, natural seedfall [414]. For details of this study, see this Research Project Summary: Forest floor and plant responses to experimental fires in an Alaskan black spruce/feather moss community.
Black spruce formed a near-monoculture in the first 2 decades after the Wickersham Dome Wildfire near Fairbanks. The fire burned 15,600 acres (6,300 ha), mostly black spruce stands ranging from 50 to 125 years old. Through postfire year 3, tree seedling establishment was variable regardless of fire severity. Low-severity areas had <50% of the ground surface blackened, litter depth reduced an average of 2.25 inches (5.7 cm), and 40% of ground vegetation alive 1 year after fire. Black spruce seedling establishment was sparse in one high-severity area, with only 20% of plots supporting black spruce seedlings 3 years after the fire. Conversely, another high-severity area contained 21,000 black spruce seedlings/ha 3 years after the fire. In low-severity areas, unburned and partially burned sphagnum mosses provided good seedbeds for black spruce. By postfire year 3, low-severity plots averaged 40,000 black spruce seedlings/ha. Black spruce seedling density peaked at postfire year 10, but 50% of black spruce establishment occurred within the first 3 postfire years. Black spruce comprised 98% of postfire tree establishment, and its density remained "nearly constant" through postfire year 20 [384].
Although black spruce generally regains prefire dominance (for example, [146,147]), competition for substrates—especially from sprouting woody species—may tip postfire succession towards dominance by other tree species. A study in central interior Alaska found no correlation between prefire black spruce basal density and postfire recruitment (r = 0.34, P>0.1), but black spruce recruitment was negatively correlated with quaking aspen regeneration (r = -0.61, P=0.01). Density of quaking aspen regeneration was positively correlated with fire severity (r = 0.49, P=0.02). The study was conducted 7 and 8 years after a summer wildfire in the Alaska Range, near Hajdukovich Creek. The prefire forest was open to closed black spruce, with occasional quaking aspen stands. The fire burned from 14 June to early September 1994. Initially, fire weather was moderate and fire severity was low. In the first 3 weeks in August, however, fire weather escalated to extreme and fire severity was high. Fire severity was assessed by satellite and confirmed on ground plots by postfire depths of organic soil layers. Of 22 stands sampled, 20 were black spruce before the fire; the other 2 were quaking aspen. The quaking aspen stands were on coarse soils; the thick organic soil layer of most sites had apparently deterred quaking aspen growth. Prefire tree age ranged from 60 to 280 years. Two fires had occurred within the previous 200 years, 1 around 1875 and 1 around 1910. Mean prefire organic depth was estimated at >10 inches (25 cm) on severely burned plots, based on depths in an adjacent, unburned forests. Postfire organic depths ranged from 0 to >8 inches (20 cm). The authors attributed differences in postfire organic depths to increasingly dry weather conditions and drying fuels—and therefore, increased consumption of the organic soil layer—as fire severity increased through the summer [211].
Great Lakes: Black spruce seeds in quickly after fire on mesic to dry pine-spruce uplands. However, jack pine and/or red pine also seeds in aggressively and generally overtops black spruce in early postfire years. Thirty-five years after a fire in a mixed-confer forest in northern Minnesota, the overstory was mostly jack pine and black spruce. Most jack pines were 33 to 34 years old and 4 to 6 inches (10-15 cm) in diameter, while most black spruces were 28 to 32 years old and only 1 to 3 inches (2.5-3 cm) in diameter [166]. Black spruce is shade tolerant and can survive suppression for more than 100 years [166], so black spruce may replace the pines in the absence of fire for centuries [46,395].
After the May 1971 Little Sioux Wildfire in northeastern Minnesota, black spruce seedlings gained biomass quickly. In postfire year 1, mean biomass of seedlings was 0.1 g. By postfire year 4, it was 10.2 g [302]. Prior to the wildfire, the area had been recently logged and was a mosaic of stands including lowland and upland black spruce, quaking aspen, jack pine, and eastern spruce budworm-infested balsam fir [342].
Western Canada: A 20-year study after a wildfire in southeastern Yukon found spruce (black spruce and white spruce) seedling density averaged ≥8 stems/m² in postfire year 10. Spruce seedling density remained constant or increased slightly from postfire years 10 to 20 (P=0.08); in contrast, quaking aspen and lodgepole pine densities declined after postfire year 10 (P<0.001). In postfire year 19, mean spruce heights ranged from 0.6 to 4.1 feet (0.2-1.3 m). Tree heights were not correlated with either total tree or individual tree species densities [206].
Although black spruce often regenerates poorly after logging (see Fire Management Considerations), it regenerated successfully in southeastern Manitoba after selective logging was followed by prescribed fire. Two black spruce/feather moss forest sites were thinned from 2,180 to 800 trees/acre in winter, then broadcast burned 2 years later, on 17 May (a low-severity fire) and 29 May (a moderate-severity fire). Black spruce seedling establishment and survival were better on the moderate-severity site than on the low-severity site. Depth of burning into the moss layer averaged 5.5 inches (14.0 cm) on the moderate-severity and 2.5 inches (6.4 cm) on the low-severity site. Five years after burning, black spruce stocking was 94% (16,129 seedlings/acre) in areas where burning depth ranged from 4 to 7 inches (10-18 cm); 70% (3,075 seedlings/acre) in areas where burning depth ranged from 2 to 3 inches (5-8 cm); and 35% (1,898 seedlings/acre) in an unburned control [80]. For details of this study, see this Research Project Summary: Black spruce experimental fires on lowland sites in Manitoba.
A prescribed surface and crown fire in a black spruce-lichen stand on the Caribou Range, Northwest Territories [9]. Photo courtesy of the Northern Forestry Centre.Eastern Canada: Black spruce dominates most boreal conifer ecosystems of this region (see Plant communities), but balsam fir and/or northern whitecedar may eventually replace black spruce if fire does not return for centuries. In open woodlands in northern Québec, black spruce tends to regenerate quickly after fire, regaining or exceeding prefire density within 30 years [354]. In the balsam fir-black spruce ecosystem of northwestern Québec, a chronosequence study found that black spruce and northern whitecedar dominated all xeric, exposed-bedrock and some morainal sites from early through late postfire succession. Black spruce frequency declined around postfire year 300; it persisted longer on xeric than on mesic sites. Across sites, balsam fir persisted longer than black spruce, and northern whitecedar persisted longer than balsam fir [46].
A study in northwestern Québec found survivorship of trees was higher after low-severity fire than after moderate-severity fire. Angers and others [19] studied tree recovery after mixed-severity fires in boreal mixedwoods. In stands codominated by black spruce and jack pine, about 60% of those conifers were still alive in postfire year 1 on plots that burned at low severity (data were pooled for the 2 conifers). Conifer survival dropped to about 45% by postfire year 9. On moderate-severity plots, conifer survival was about 20% in postfire year 1 and 8% in postfire year 9. Where conifers and hardwood species codominated, overall tree survival on low-severity plots averaged about 42% in postfire year 1 and 20% in postfire year 9. On moderate-severity plots, overall tree survival averaged about 5% in postfire year 9 [19].
In southern Labrador, black spruce's postfire seedling establishment progresses slowly for 70 to 100 years, resulting in uneven-aged stands. Within spruce stands in this coastal climate, fires generally consume very little organic matter and leave only charred humus. For the first 20 years after fire, black spruce seedling establishment is sporadic and largely restricted to depressions, the edges of water courses, and exposed mineral soils [128].
Black spruce forests are highly flammable: They are the most flammable vegetation types in boreal Alaska [85] and Canada [15]. Jack pine-black spruce forests of the Great Lakes region and Maine are considered the second most flammable ecosystem in the United States, next to chaparral (Frelich personal communication cited in [228,229]). Among black spruce types, upland black spruce stands are generally most flammable and black spruce bogs the least [122]. Fuel loads are usually lower in black spruce-lichen woodlands than in black spruce forests because woodland stands are more park-like and open, often with a component of less flammable white spruce [385]. However, black spruce woodlands can have large accumulations of fine fuels, sometimes >50 tons/acre. During warm summers, these fine fuels dry and become flammable very rapidly [52].
Because they are typically wet, lowland black spruce bogs cannot usually carry fire [122] and serve as firebreaks [233] in most years. However, lowland bogs burn in extreme fire years [122]. In Quetico Provincial Park, Ontario, an August 1995 wildfire burned through old-growth red spruce-eastern white pine stands (200-300 years old) into black spruce lowlands that "would normally be considered fire breaks". The crown fire burned 62,000 acres (25,000 ha) and was largest and "most significant" fire in the Park since 1936. Intensity was estimated to have reached 40,000 kW/m in some red pine-eastern white pine stands [267].
Chemical content and arrangement [56] of fuels make black spruce forests highly susceptible to crown fires. Black spruce trees are highly flammable [85,266]. Todd and Jewkes [368] report that black spruces "are an ideal fuel for spreading fire". Black spruces have resinous needles and cones [85,396] and considerable pitch in their wood [368]. Their twigs and needles are "tougher and gummier"—with more resins—than those of white spruce [396]. Branches are usually retained after they die [122,383], encouraging fire spread into crowns [383]. Because black spruce needles are fine and highly flammable fuels, they combust and are consumed in 1 or 2 minutes [37]. Eastern dwarf mistletoe infections increase flammability of black spruce (review by [13]) (see Fire Management Considerations).
Typically, stand structure of black spruce forests provides vertical continuity of surface and ladder fuels [56,85]. Cronan and others [85] report that in black spruce communities, the "combination of continuous surface fuels, frequent ladder fuels, and flammable canopy fuels creates optimal conditions for high-intensity crown fires that can initiate across a wide gradient of weather". The forest floor under most black spruce stands is made up of a thick mat of decomposed organic material [104] and live mosses and lichens. In summer, the mosses and lichens "become dry and tinderlike" [263]. Feather mosses [85] and ground lichens [263] provide surface fuels that can dry out rapidly, becoming highly flammable [85,263]. Because feather mosses retain moisture better than lichens, flammability of surface fuels may decrease with succession as feather mosses replace lichens. Permafrost slows drying of feather mosses [127]. In mature (>50 years) black spruce-lichen tundra communities, lichens often form a continuous mat that ensures surface fuel continuity. These communities are highly flammable, with low rates of decomposition on the forest floor [28]. Typically, most of the litter and much of the soil organic matter are consumed during fire, exposing 30% to 40% of the mineral soil (review by [28]). On the Caribou-Poker Creek Experimental Watershed, Hylocomium feather mosses dried out faster than Schreber's moss, possibly because Hylocomiums have more vertical structure and better drainage. Moisture levels at the surface of the forest floor were more spatially variable in May than in June and July. After the moss layer had dried, it required a "significant rainfall" to rehydrate: Intermittent light rains had little effect on moss moisture levels [116].
Branches of individual black spruces are dense, often extending to the ground [104,368,383]. These branches are ladder fuels, and once fire crowns, it "intensifies and spreads rapidly" [368]. Low, ericaceous shrubs may also carry flames to tree crowns [56,85,383]. Ericaceous shrubs such as black huckleberry, sheep-laurel, and bog blueberry have a high percentage of ether extracts and lipids [28] and are highly flammable [28,383]. They may carry flames 2 to 3 feet (0.5- 1 m) above the soil surface. From that point, black spruce's dead or live lower branches usually carry fire to tree crowns [383]. The branches are often draped with arboreal lichens, which also carry flames to the crown [263,264]. Dyrness and others [103,393] reported that in open-canopy black spruce communities with feather mosses and lichens, a shrub layer is not critical for continuity of ladder fuels; fire easily moves from the moss-lichen ground layer to black spruce canopies.
Johnstone (2008 in [65]) noted that because plant community flammability and fire severity are less in hardwood than in black spruce types, "increasing the proportion of deciduous dominated stands across the landscape reduces the probability of severe fire, not only for deciduous trees but ultimately for black spruce too". Deciduous patches in a black spruce matrix can serve as fire breaks [65].
Woody debris loads are high after crown fires in black spruce stands, and live stands usually accumulate deep organic soil layers [404]. Mutch [295] suggested that accumulation of windfall and other fuels over long time periods renders black spruce communities highly flammable and predisposed to large fires during drought years. In the Northwest Territories, structure of a ~300-year-old black spruce forest was open, with stunted trees and a "high amount of standing dead matter" [301]. In interior Alaska, the litter layer of a black spruce/feather moss-lichen forest had greater mass, was more acidic, and contained fewer total nutrients than the litter layer beneath a quaking aspen-paper birch forest [372].
Moss biomass may be high in all stages of postfire succession in black spruce communities, while snag density tends to decrease and downed woody debris tends to increase over time. In a chronosequence of fuel accumulation in black spruce stands of north-central Manitoba, 8% to 20% of downed woody fuels [273] were completely covered by sphagnum [59] and/or feather mosses [57] in stands of all ages. For stands >70 years old, up to 26% of downed woody fuels were partially to fully buried by mosses. Loads of downed woody debris were greatest from postfire years 20 to 40. Standing dead woody fuels were prevalent before then [273]. Coarse woody debris loads ranged from 9.7 Mg/ha in 43- and 77-year-old stands to 80.4 Mg/ha in an 18-year-old stand. Snag fall was 3 times more frequent in a 12-year-old stand (9.8%/year) than in a 9-year-old stand (2.9%/year) [58]. Net primary production peaked in 12- to 20-year-old stands, and primary production of trees peaked in 37-year-old stands, with both net and tree primary production greater on well-drained than poorly drained burns. In 37-year-old stands, most tree biomass was from sprouting hardwood species such as quaking aspen [59].
Several studies sequenced decay and falling rates of black spruce and other snags. In Labrador, biomass of woody debris in burned black spruce forests peaked around postfire year 20, mostly due to snag fall. The authors provide a model for predicting merchantable wood volume for young (<10-year) to old-growth (>181-year) black spruce stands [154]. In northwestern Québec, most wildfire-burned black spruce snags fell within 19 years of tree death, a rate similar to that of balsam fir. Quaking aspen snags fell quickest (x̄ =15 years), while jack pine snags stood the longest (x̄ =26 years). Nearly all black spruce snags had fallen within 40 years of tree death [20]. For black spruce, snags fell sooner on plots that burned at low severity than on plots that burned at high severity (P<0.0001) [19]. A study near James Bay, Québec, had similar findings. Decomposition rates were slowest for severely burned black spruce snags and highest for lightly burned black spruce logs. The authors found that black spruce snags that burned at high severity shed their bark fastest and had lowest moisture contents, which slowed decay [62]. Rapid decay rates of snags that burned at low severity might be due to wood tunneling by wood-feeding insects and subsequent infections of wood-colonizing fungi [62,341].
In mixedwood stands, boreal hardwood trees are less flammable than associated conifers, including black spruce [170]. A fire history study found that fire was a relatively unimportant disturbance in interior Alaska until about 5,500 years BP, when black spruce replaced birch-alder as the dominant community type in the region [266]. In mixedwood forests, flammability tends to increase as the conifer component of the forest increases [183]. In early postfire stages, however, fuel loads may be greater in hardwood than in black spruce forests. In interior Alaska, total woody fuel loads from postfire years 1 to 5 averaged more in paper birch than in black spruce communities. From postfire years 6 to 25, large woody debris loads were greater in paper birch than black spruce stands, but there were more small-diameter woody fuels in black spruce. After that, black spruce stands had more total downed woody fuels than paper birch stands. Fuel loads in black spruce-hardwood stands were intermediate except from postfire years 51 to 100, when large woody debris loads were greater in mixed stands than in either paper birch or black spruce stands [122].
Woody fuels loads (T/ha) of black spruce and paper birch communities in interior Alaska. Cells are empty where data were not reported [122]. Postfire years 1-5 6-25 26-50 51-100 >100 Black spruce Small-diameter7.4 Large-diameter 10.2 Total 4.9 8.1 5.7 7.3 Paper birch Small-diameter 5.3 Large-diameter 28.8 Total 16.3 5.4 5.2 5.0
Distribution and loading of fuel biomass differ with successional stage and substrate moisture. Early-seral herb and shrub stages have less continuous fuels than later-successional, even-aged black spruce stands [368]. In southeastern Labrador, open black spruce-balsam fir forests from 40 to 90 years old were the most flammable vegetation types. At that seral stage, stands were composed of scattered, mature trees; a "fairly luxuriant" shrub layer of bog Labrador tea and sheep-laurel; and a nearly continuous ground layer of reindeer lichens [127]. Surface fuels may increase with soil moisture due to increasing cover of lichens and ericaceous shrubs [385]. Chronosequence surveys near Delta Junction in interior Alaska found biomass production of black spruce communities—including biomass of lichens, feather mosses, and vascular plants—differed with substrate moisture. On dry sites, mean maximum production peaked in a young stand (15 years old) at 410 g/m²/year. On mesic sites, it peaked in a mature stand (>100 years old) at 335 g/m²/year. Production in the young stand was mostly sprouting shrubs, while it was mostly black spruce in the mature stand [269].
Blowdowns resulting from extreme nor'easters can greatly increase loads of downed woody debris in coniferous forests with black spruce. In a review, Flannigan and others [118] noted that an extreme windstorm is "not a rare event" in the Great Lakes region. Windspeeds of ≥60 miles (90 km)/hour occur every 5 to 10 years in Minnesota [118]. In northwestern Ontario, a 1973 tornado in jack pine-black spruce was followed by a 1974 wildfire that consumed blowdown fuels on 79,000 acres (32,000 ha) [118]. A blowdown on 4 July 1999 affected nearly 500,000 acres (200,000 ha) on the Superior National Forest, Michigan. Fuel loads in the Boundary Waters Canoe Area increased from 5-20 tons/acre to 50-100 tons/acre as a result. A blowdown of this size, and the consequent 5- to 10-fold increase in fuel loads, was historically unprecedented. A "very severe prescribed fire" was conducted in September 2002 to reduce fuel loads in the area. The prescribed fire was credited for helping contain the 2006 Cavity Lake Wildfire within the wilderness area. It was a "very high intensity fire" that "burned the soil down to bedrock in some areas", exposing pink granite. In contrast, the 2007, human-ignited Ham Lake Wildfire occurred in an untreated part of the blowdown outside the wilderness and burned 160 structures. The author suggested that climate change may increase the likelihood of severe weather events such as the 1999 blowdown [250].
Several studies across black spruce's distribution measured fuel loads in various strata of black spruce stands. Barney and others [33] provide forest floor fuel loads, depths, and bulk densities for upland and lowland black spruce types of interior Alaska.
In black spruce/Easter snow lichen woodlands of the Northwest Territories, active crown fire developed on 2 plots with crown bulk densities of 0.12 and 0.17 kg/m³ and rates of fire spread of 26.3 and 33.3 m/minute. Active crown fires did not develop on 6 other plots even though crown bulk densities were higher (0.18-0.32 kg/m³); on these plots, rates of fire spread were lower (1.2-6.1 m/minute) (review by [151]).
In Alberta, annual peat accumulation on 2 black spruce/sphagnum bogs ranged from 156 g/m² to 257 g/m². Accumulation was similar on hummocks and in hollows on the Sinkhole Lake Bog, but peat accumulated more rapidly on hummocks than in hollows on the Athabasca Bog. Dark sphagnum dominated the ground layer of hummocks, while lichens, true mosses (Bryopsida), and wet-loving sphagnum species such as narrow-leaved sphagnum dominated the ground layer of hollows [39].
In Newfoundland, litterfall in a mature, 70-year-old black spruce/feather moss forest ranged from 2.4 to 3.5 Mg/ha/year before clearcutting and from 0.2 to 0.3 Mg/ha/year after clearcutting. Rates of litter decay did not differ significantly between uncut and cut plots for 2 to 4.5 years after clearcutting. Splendid feather moss, Schreber's moss, and knight's-plume moss dominated the groundlayer, and there was a balsam fir-hardwood component in the overstory [291].
Zasada and others [103,413,414] demonstrated that feather moss and lichen fuels on the forest floor carry the surface portion of mixed-severity fires in black spruce/feather moss types. Downed woody fuels were too sparse to have much impact on fire spread on the forest floor. The "upper portion of the forest floor readily carried fire across most of every unit" [103]. From there, low branches on black spruce easily carried fire into tree crowns. These experimental fires created a mosaic similar to that created by the mosaic fires typical of black spruce/feather moss forests of interior Alaska. The authors concluded that "wildfires burning on sites similar to the experimental area and within the ranges of variables documented" in their study should produce similar fire behavior and effects on vegetation and soils [103]. For details of this study, see this Research Project Summary: Forest floor and plant responses to experimental fires in an Alaskan black spruce/feather moss community.
Models: Researchers have developed many models to help quantify fuels, decay rates, mortality, and fire behavior in black spruce stands. Models are listed below by region and purpose.
General for the United States and Canada:Viability of fresh black spruce seed is high, but viability of cone-stored seed drops with age. A variety of substrates may support germination, although rates are generally best on mineral or deeply charred organic soil.
Viability: Coned-stored seeds remain viable for several years [2]. Viability of fresh seed averages about 88% [340]. Some seeds may remain in cones for up to 20 years, but viability drops to nearly zero after about 15 years [174]. A Newfoundland study found viability of crown-stored black spruce seed remained above 90% for 12 years but dropped rapidly after that (review by [395]). In northeastern Ontario, viability of filled seed collected from unburned cones averaged 53% for 1- to 5-year-old seed; 20% for 6- to 10-year-old seed; and 5% for 11- to 15-year-old seed [152].
Seed viability apparently drops quickly after fire opens cones [406]. After the 1971 Wickersham Dome Wildfire in Alaska, germination dropped from 65% for seeds collected in postfire year 1 to 32% for seeds collected in postfire year 2 [411]. After a wildfire at the boreal-arctic interface, Northwest Territories, germination of black spruce seed ranged from 0% to 19% from postfire years 0 to 6 but was ≤1% in postfire year 20 [403]. On burned sites near James Bay, western Québec, black spruce establishment averaged about 4,000 seedlings/ha in postfire year 4, but cone-stored seed was no longer viable and establishment was poor by postfire year 10 [235].
Severe fire kills some of coned-stored seed and apparently reduces overall germination rates of dispersed seed. After the Wickersham Dome Wildfire, germination rates of black spruce seed were significantly higher (P=0.5) on unburned (77%) and low-severity plots (87%, not all needles consumed and some remained green) compared to severely burned plots (54%, needles and fine branches consumed). Researchers collected seeds from postfire months 2 through 12 [411].
Recruitment failure can be due to a lack of seed sources [8] resulting from very short fire-return intervals or due to thick organic soil layers. Natural regeneration of black spruce was poor on a reburned Yukon site that had burned in 1990 or 1991 and again in 2005. The site was artificially seeded to black spruce 3 or 4 years after the last fire. Artificial regeneration resulting from the seeding was similar to or greater than natural establishment on a black spruce site that had burned 94 years prior and therefore had a crown-stored seed bank. Recruitment was poor after artificial seeding of an untreated, 76-year-old stand with a thick moss and lichen layers on the organic horizon. The authors attributed the poor establishment to thick organic horizon layers [64].
Black spruce establishment is generally poor after clearcutting that occurs before seeds disperse (see Seasonal Development) [66,260] or when cone-bearing branches are burned in piles rather than broadcast burned [263]. See the Very frequent fires section of Fire Management Considerations for more information on this topic.
Seed production and viability may be low in the northernmost limits of black spruce's distribution [55,113]. Few trees produced cones near the arctic treeline on the southern Brooks Range, Alaska. Of seeds collected, only 2% germinated in the greenhouse [256].
Seedbeds: Best establishment generally occurs on mineral or thin organic soil. When the seedbed is continually moist, black spruce may successfully germinate on either mineral soil, organic soil, or sphagnum [86,174,255,395]. Germination proceeds "rather quickly" under continually moist conditions. The germination period may be longer if the seedbed substrate dries and re-wets during germination [243].
Fire prepares favorable seedbeds by removing soil organic horizons [54,55], lichen and moss mats [28], other competing vegetation, and by blackening and warming the soil [54,55]. Several authors reported that mineral soil or a thin humus layer provides an ideal seedbed for black spruce [2,22,332]. Generally, severe fires result in good black spruce establishment. On upland burned sites in interior Alaska, good germination occurred on moderately burned (various levels of organic matter burned off but mineral soil not exposed) to heavily burned (mineral soil exposed) sites, while lightly burned (organic layer only scorched) and unburned sites had no black spruce germinants [414]. On 4 sites in interior Alaska and Yukon, plots burned at different severities were then artificially seeded to determine how fire severity affects black spruce's postfire establishment. Although some establishment occurred on unburned plots or plots burned at low severity, black spruce required about 6 times as much seed by weight to produce a viable seedling on unburned organic soil compared to mineral soil. Seedling establishment was negatively associated with depth of the organic soil layer (P<0.025). The authors attributed this to the unstable moisture supply and frequent drought stress of organic soils. However, establishment was lower on the most severely burned site (ash layer with no organic material remaining) than on sites where severe fires left some residual organic material and no ash layer. Establishment was also greater on manually cleared mineral soil than on the most severely burned site. The authors suggested that on the severely burned site, a water-repellant ash layer reduced moisture availability at the soil surface [202]. On a burn in northwestern Québec, black spruce recruitment was highest on skid trails, followed by mineral soil, then very thin charred organic soil. Charred moss, charred sphagnum, and leaf litter had the fewest black spruce germinants [149].
On a 30-year-old burn in Alberta, most black spruces established in rotten wood (40%). About 25% established in mineral soil [245].
A review noted that sphagnums often provide good seedbeds for black spruce. Fire is not always needed for good black spruce establishment on sphagnum seedbeds, although it may help clear a seedbed covered with downed woody debris or slash. In contrast, feather moss is often an unfavorable seedbed, and moderate to severe fire that reduces the feather moss layer is usually required for good black spruce establishment [22]. Sphagnums likely provide a favorable seedbed due to their high capacity to hold moisture: they can absorb about 20 times their dry mass in water [325].
Hydrophobic soil or a heavy ash layer inhibits black spruce germination. After severe fire creates those conditions, the soil must regain permeability before black spruce can successfully germinate and establish. In southeastern Manitoba, black spruce seed hand-sown on wildfire-burned plots showed better establishment in postfire year 3, after mosses and lichens had colonized the mineral soil, than in postfire year 1, when mineral soil was covered by an ash layer [217]. In central Alberta, highest black spruce establishment occurred in postfire year 7, with few trees establishing in postfire year 1. The author attributed this to presence of an inhibitory ash layer in the first few postfire years [252]. Rowe [332] reported that in Riding Mountain National Park, Manitoba, a wildfire in the 1940s—fueled by live vegetation and heavy downed woody debris from a blowdown—left a thick ash layer. By the late 1960s, black spruce had established in "patches of vigorous saplings...conforming to the fired areas". The relatively heavier seeds of black spruce withstood desiccation better than the lightweight seeds of quaking aspen and birch, so even on organic soils, black spruce had higher rates of establishment than the hardwoods [110].
In the foothills of Alberta, "practically all stands containing black spruce over the whole range of sites can be traced back to fire origin. As a result, the stand structure is generally even-aged" [174]. After fires in the summer of 2004 in interior Alaska, surveys conducted in 2005 on 90 burn sites found nearly 100% mortality of black spruce. Based on percent consumption of the organic soil layer, most of these sites burned at high severity [173]. Refer to FIRE REGIMES for detailed discussions of fire severity and patterns of burning in black spruce communities.
Although fires are usually fatal, some black spruce individuals may not torch. In north-central Alberta, Kiil [220] reported that although 100% of black spruces died as a result of an 18 July prescribed fire, only about 54% of black spruce crowns caught fire. Torching of individual black spruces became "increasingly frequent" 10 to 15 minutes after ignition. For trees that were scorched but did not torch, mean scorch height was 9.5 feet (2.9 m). Trees usually torched if scorch height reached more than 16 feet (5 m). Depth of burn into the organic soil layer averaged 3.2 inches (8.1 cm); this completely removed the ground cover of reindeer lichens [220].
On wet to mesic sites, black spruces in clumps or in the interior of stands may escape fire [37,383], leaving a patchwork of stringers or smaller clumps. Foote [124] noted live black spruce stringers on newly burned, mesic black spruce sites in interior Alaska [124]. Lutz [262] reported that in interior Alaska, extensive "upland areas of black spruce are occasionally seen where a fire has killed literally every tree. On relatively wet lowland areas the likelihood of complete destruction of stands is much less. There are individual trees, and trees in irregular groups and stringers, (that) are likely to survive" [262].
Some individual black spruces may survive fire [169] with scarring. Foote [124] noted live, fire-scarred black spruces in black spruce/bog blueberry-bog Labrador tea/splendid feather moss forests of interior Alaska. Scarred trees were either standing alone or in stringers [124]. Some scarred spruces were also found by the Tanana River, Alaska, although the spruces were not identified to species [274]. Rowe and others [335] found a few fire-scarred black spruces in jack pine-black spruce forests in the Northwest Territories. They suggested that scarring was from lingering ground fires that "creep through the peat plateaus in the years after some major conflagration" [335]. In southern Québec, live, fire-scarred black spruces were found in black spruce-lichen woodlands that had stand-replacement fires >100 years prior. The fire scars were thought to have been caused by surface fires that followed stand-replacement fires [141]. Some fire-scarred black spruces were found near arctic treeline in Québec, but the authors noted that fire scars "were rare because subarctic (black) spruces usually display dense foliage at the stem base that is susceptible to burning completely during fire" [298].
Black spruce is most likely to survive low-severity surface fire that leaves unburned patches [205,383]. On 10 sites across interior Alaska that burned in the severe fire years of 2004 or 2005, fires crowned in all stands but effects to the organic soil layer varied from low to high severity. Vegetation and soil data were collected in 2005. Some black spruce foliage remained unconsumed on burn edges or within small islands, and some trees on low-severity plots were alive in either postfire year 1 (for 2004 fires) or postfire week 6 (for 2005 fires). All black spruces on moderately-burned plots were dead. On moderate-severity plots, boles showed "significant charring" and on average, foliage on >50% of stems in tree canopies was consumed. Moderate-severity sites had 30% to 50% mean reduction in total depth of the organic soil layer, and >90% of the layer was charred. High-severity sites had an 80% to 100% average reduction in total depth of the organic soil layer [213].
Despite these exceptions, it is important to note that even low-severity fires typically kill most—or all—black spruces in a stand. Hanson [159] found that all black spruce trees were killed following a low-severity surface fire in an open black spruce-tamarack community in interior Alaska. The site contained 81 to 162 trees/acre; trees ranged from 40 to 178 years old and 1.5 to 3 inches (4-7 cm) in diameter. The fire consumed the top 2 to 4 inches (5-10 cm) of the 6- to 14-inch (15-35 cm) soil organic layer [159].
Effect on seed: Most cone-stored black spruce seeds survive fire. Even though fires usually crown in black spruce stands, they are rarely so hot that all seeds are killed ([263,388], review by [2]). Crown fires kill some seeds [203,208,410,411], but most survive because of the compact nature of individual cones [410] and the tightly packed arrangement of cones on the branch-dense crown [37,243,410]. A study conducted in northern Québec suggests that black spruce cones are more fire-resistant than the fully serotinous cones of jack pine [24]. Mortality of black spruce seeds increases with fire temperature; however, high temperatures also increase the rate of cone opening, ensuring that surviving seeds disperse soon after fire [208,410].
Black spruce seeds subjected to high, prolonged temperatures or those in short-statured individuals are most vulnerable to fire mortality. LeBarron [243] observed that black spruce did not regenerate after slash fires in clearcuts. He concluded that the "intense and prolonged heat" of slash fires kills black spruce seeds [243]. Fire often kills the seed crop of short trees. Natural selection for fast-growing, tall black spruces may occur in areas with fire-return intervals of 100 years [2] or less.
Seed rain of black spruce is usually greatest immediately or soon after fire, with lower levels over ~5 postfire years [410]. Snags, surviving black spruces, and adjacent stands provide seed sources [262]. See Seed dispersal for further information.
Many wildlife species use black spruce communities. Mammals using black spruce communities as habitat include moose [251,311], caribou [209,355], American martens [18,309,311], and American minks [311]. A variety of bird species [311] use black spruce communities, including woodpecker and sparrow species [156], great grey owls [306], and northern hawk owls [157].
See Appendix C for links to FEIS reviews available for animal species mentioned in this section.
Many wildlife species are adapted to particular successional stages in black spruce communities. For example, moose [164,251,268], snowshoe hares [164,215], black-backed woodpeckers [176,222,294,298], and other woodpeckers [294,298] use early postfire stages. American martens use midseral [234] and late-seral [18,143,144] black spruce communities. Woodland caribou use late-seral black spruce communities as winter habitat and forage on arboreal lichens draping black spruce branches [77].
Some wildlife species move between and use different-aged black spruce stands. For example, woodland caribou use open burns when migrating and as predator escape routes [284]. A study in central-interior Alaska found snowshoe hares and Canada lynx preferred 30-year-old (midseral) black spruce forests and woodlands, but the authors noted that Canada lynx might use late-seral black spruce stands during denning and when snowshoe hare numbers are low [310].
Postfire population trends of mammals, birds, herptiles, fish, and arthropods using black spruce communities follow:
In north-central Ontario, deer mouse populations increased after logging and slash fires in black spruce forests. Southern red-back vole populations declined [277].
Short-term studies in the Great Lakes region showed postfire shifts in bird guilds, a temporary decrease in small mammals, habitat improvements for larger mammals, and no effect on fish populations. Surveys in northeastern Minnesota found foliage gleaners such as Blackburnian warbler were most important in a 70-year-old jack pine-black spruce stand. A wildfire burned the stand in August 1976. In May 1977, ground- and shrub-foragers such as gray-cheeked thrush had become most important [21]. A study conducted 3 years after a 1979 wildfire on the Seney National Wildlife Refuge, Michigan, also found postfire shifts in bird guilds. The fire created a mosaic of open bogs in lowlands interspersed with tamarack-black spruce-red maple peatlands on uplands. In postfire year 3, bird species that forage in early-seral forests, especially brown thrashers and song sparrows, used the upland peatlands. Small mammal numbers dropped the fall after the fire, and no small mammal species used burned areas more than unburned areas. Small mammal numbers increased 17-fold in the second postfire fall. By postfire year 3, American beavers were concentrating in alder thickets, which were dense with new sprouts. Likely due to heavy berry crops, survival of American black bear cubs was good in postfire year 3. An inventory in postfire year 2 showed no significant postfire drop in northern pike, yellow perch, or brown bullhead populations. This was attributed to the ability of remaining peat to hold silt and minerals, leaving the mineral content of the water similar to that of prefire levels [17].
Great gray owl partially hidden behind a black spruce bole. Photo ©Sparky Stensaas,Newly burned black spruces provide foraging opportunities for insectivorous birds, snags for cavity nesters, and open structure for foraging raptors. A study comparing bird use on 1) unburned, 2) burned, and 3) burned and salvage logged sites in mixedwoods of Alberta found that the 3 sites supported distinctly different assemblages. Canopy nesters, cavity nesters, and insectivores (for example, yellow-rumped warbler, boreal chickadee, ovenbird, respectively) were most common in burns and least likely to use burned and salvage logged sites. Ground nesters, shrub nesters, omnivores, and habitat generalists (for example, white-throated sparrow, chipping sparrow, gray jay, and dark-eyed junco, respectively) were most common in burned and salvage logged sites. The mixedwoods were a mosaic of jack pine and quaking aspen on uplands and black spruce and tamarack on lowlands. The wildfire occurred in the summer of 1995, and salvage logging was conducted in postfire year 2. Bird surveys were conducted in the spring and summer of postfire year 3 [289].
Bird counts in black spruce/feather moss forests of southern Québec showed woodpeckers were abundant in early postfire succession. Secondary cavity nesters such as boreal chickadees and brown creepers were most abundant in mid- and late succession [258]. Overall, bird species diversity was 60% higher 30 years after a wildfire than before in a jack pine-black spruce forest in the Boundary Waters Canoe Area. From postfire years 1 through 5, the number of primary and secondary cavity nesters—such as black-backed woodpeckers and tree swallows, respectively—increased. Because shrub cover increased in early postfire years, the importance of shrub-foraging species such as white-throated sparrow and chipping sparrow also increased. The forest was 73 years old prior to the late-August, lightning-ignited fire that burned 554 acres (1,368 ha). Permanent plots had been established the year before the wildfire [156].
In boreal black spruce forests of east-central Alberta, northern hawk owls used burned snags in early postfire seres for perching and nesting. Their abundance was negatively associated with time since fire (P=0.05), and no northern hawk owls were detected in forests >110 years old. Based on surveys and a model, the authors suggested that burned black spruce forests were suitable northern hawk owl habitat only until around postfire year 8 [157].
Few studies were available on herptile use of black spruce communities. In a New York study, the eastern massasauga rattlesnake [194], a Federal Candidate species [377], was found exclusively within open portions of a black spruce-tamarack-heathland that had been logged and pile-burned a year prior [194].
Fire in subarctic black spruce/sphagnum forests apparently had little effect on small-lake fish populations of Alberta. Two years after summer wildfires, <3% of the variation in fish assemblages in 6 small lakes within a burned area was due to disturbance (fire alone or fire and salvage logging). The fish assemblages in the burned area were compared to those within an adjacent unburned area encompassing 9 lakes. The difference in population sizes was not statistically significant (P=0.18). However, white sucker populations were slightly higher [370] and artic grayling slightly lower [369] in lakes within the burned area than in lakes in the adjacent unburned area.
Arthropod guilds use burned and unburned black spruce habitats based, in part, on their foraging or hunting strategies. Several families of beetles (for example, Buprestidae) contain species that are obligate feeders on dead or decaying wood [140,298,341]. These beetles congregate in recent burns, and woodpeckers prey upon them. In black spruce/feather moss stands of northwestern Québec, wood-feeding beetles were found in areas that burned from low to high severity. They were most abundant where fire severity was low [298]. In Grand-Jardins Provincial Park, Québec, stalking spiders were positively associated with burns and clearcuts, while web builders were about equally common on burns, clearcuts, and undisturbed sites. Total spider species diversity was greater on burns and clearcuts than on unburned sites (P≤0.01 for all variables) [232].
Palatability and nutritional value: Wild ungulates and livestock rarely browse black spruce. Moose occasionally browse saplings [129,412], but white-tailed deer browse black spruce only under starvation conditions [129]. Barren grounds caribou use black spruce-lichen woodlands and black spruce/shrub forests as winter rangeland [345].
Black spruce is important browse for some small mammals and bird species. It is a major food of snowshoe hares, especially in winter. Snowshoe hares in interior Alaska consume black spruce's bark, twigs, and needles most heavily in fall and winter [407]. Near Yellowknife, Northwest Territories, they browsed the bark of charred black spruces more than expected based on availability (P>0.05). The study was conducted August, in a black spruce-paper birch-tamarack forest that had burned 1 year prior [357]. Spruce grouse feed entirely on spruce needles during winter. In Alaska, they eat spruce needles from early November through March [109].
See Ellison [109] for information on the nutritional content of black spruce needles.
Numerous mammals and birds feed on black spruce seed. Red squirrels harvest the cones and eat the seeds within [113,243,263,412]. Mice, voles, shrews, and chipmunks consume seeds off the ground. Chickadees, nuthatches, crossbills, grosbeaks, and the pine siskin extract seeds from open spruce cones and eat seeds off the ground [155,200].
Black spruce seeds do not provide as much energy as white spruce seeds. In Alaska, black spruce seeds averaged 6,053 cal/g, about 9% fewer calories than white spruce seeds [63].
Cover value: Black spruce provides good cover for moose. It often grows in dense stands and on moist substrates, conditions that provide cool bedding in summer [14]. Black spruce also provides good cover for spruce grouse [199]. In the Great Lakes states, spruce grouse use black spruce stands regularly [200].
The ruby-crowned kinglet, magnolia warbler, Cape May warbler, and ovenbird commonly nest in black spruces in the Great Lakes region [200].
Logging:
Tree harvest may be used as a fire surrogate on sites where prescribed fire is not possible or desired. In the long term, however, even-aged management of black spruce forests will likely result in loss of old growth, reduced stand structure variability, and reduced biodiversity. On fire-excluded sites, Bergeron and others [44,45] advocate using silvicultural techniques that allow for the full spectrum of age classes and stand structures across a landscape. Because harvesting trees does not mimic all the effects of fire ecologically (for example, no reduction of soil organic matter and no increases in soil nutrients) [45,51], they suggest using such management only in small acreages [45]. A mix of clearcuts, partial cuts, and selective cuts may best create diverse stand structures similar to those of areas where fire is not excluded. Clearcutting followed by planting or seeding can create an even-aged structure similar to that of young and mature stands. Partial cutting can simulate structure of old growth, and selective cutting can create gaps, mimicking gap dynamics
in old growth [49].
A study across 30,956 miles² (57,332 km²) in eastern Québec found that generally, balsam fir dominated stands originated after clearcutting; quaking aspen and paper birch dominated stands originating after clearcutting followed by wildfire; and black spruce dominated stands originating after fire (prescribed or wild). Sites subjected to clearcutting from 1920 to 2000 or to burning from 1800 to 2000 were selected for study [61].
Not all studies indicate that fire is important for black spruce regeneration. In a mixedwood forest near Thunder Bay, Ontario, black spruce establishment was greater 5 to 15 years after clearcutting (~190 trees/ha) than 5 to 15 years after fire (~60 trees/ha). The researchers concluded that for black spruce, the "natural regeneration process after fire appears to be emulated by clearcutting". Density of black spruce after disturbance was positively related to its density before disturbance (P<0.001) [180].
Eastern dwarf mistletoe:
Eastern dwarf mistletoe is the most serious disease of black spruce in the Great Lakes states and eastern Canada [129,395]. A 1986 publication estimated that 10% to 20% of black spruce in the Great Lakes states was infested with eastern dwarf mistletoe [135]. It is less frequent in the West, and it is absent in northwestern Canada and Alaska [129,376,395]. Infection results in reduced vigor, witches' brooms, deformed trees, and death. Control is possible through silvicultural treatments and use of fire [129,395]
(see Fire Management Considerations).
Other damaging agents: Black spruce is susceptible to numerous needle rusts, fungi, and insect infestations that result in defoliation, reduced vigor, or death. These diseases usually remain at low levels but may become epidemic [395]. Wind breakage caused by butt and heart rots is common in 70- to 100-year-old stands on uplands and 100- to 130-year-old stands on low peatlands [129,199]. The eastern spruce budworm
defoliates black spruce; however, black spruce is less susceptible than balsam fir, white spruce, or red spruce. Black spruce trees most likely to be attacked are those growing with balsam fir and white spruce [129]. Numerous other insects attack black spruce but only occasionally cause serious damage [129,395].
Climate change and distributions of black spruce communities:
Black spruce and adjacent boreal ecosystems are expected to be disproportionately affected by climate change (for example, [75,76,85]). With warming temperatures, black spruce is apparently expanding into some tundra communities (e.g., [30,35,75]). In some boreal regions, reduced permafrost layers have favored hardwood species at the expense of black spruce [75,173,207]. Some boreal wetlands are drying out, reducing the area available for black spruce bogs. In lowlands of the Kenai Peninsula, Alaska, cover of black spruce-white spruce-quaking aspen forests increased while cover of open wetlands decreased from 1950 to 1996, and two-thirds of water bodies showed loss of area. The authors stated that "it appears likely that climate change is driving wetland drying and vegetative shifts to predominantly woodland and forest" [221]. See Fire Management Considerations and FIRE REGIMES of Alaskan black spruce communities
for further discussions on this topic.
Across black spruce's range, new growth begins in late spring and ends in August [129]. Cones open for pollination soon after needle flush and ripen around the time annual growth stops. Seeds ripen and disperse by late summer or early fall, about 3 months after pollination [395].
Seeds disperse either soon after a fire or when ambient air temperatures are warm enough to partially open cones [174]. Cones usually remain attached to and disseminate seeds from burned trees, but sometimes break off after burning. In northern Québec, black spruces burned by a June wildfire had dropped many of their cones by August [37].
Seed rain may occur at any time of year [174,383], but it is greatest in winter and spring and lowest in fall [395]. In northeastern Ontario, 58% of annual seed rain occurred March, April, and May [152]. In Minnesota, proportions of annual seed rain were: 9% in August; 19% in September; 38% from October through April; 13% in May; 14% in June; and 7% in July [129].
Limited data show a spring and summer germination period for black spruce seeds. In northern Québec, seeds hand-sown in late July germinated either just before frost in early summer or after snowmelt in spring. For seeds that germinated, most had done so by May [351]. After winter tree harvest and a follow-up spring prescribed fire in Alberta, most (70%) black spruce germinants emerged in June. About 23% emerged in July and 7% in August [42].
Black spruce seedlings require open conditions for optimal growth [86]. Although the seedlings are shade tolerant, growth is fastest in full sun [199]. Black spruce is often slow-growing [2,243,396]. Seedlings rarely grow more than 1 inch (2.5 cm) in their first growing season. Three-year-old seedlings are commonly 3 to 5 inches (8-13 cm) tall [129]. Roots of 1st-year seedlings may penetrate to 2 inches (5 cm) in upland soils, but roots growing in mosses rarely reach 1.5 inches (3.8 cm) deep in their second year [129].
In a 35-year-old black spruce peatland in north-central Alberta, black spruces that established in the first postfire decade grew faster than those that established later. Most established in postfire years 4 to 7, with little recruitment after postfire year 25. Height growth was "nearly constant" over tree life, although large black spruces tended to attain height growth faster than small black spruces. Most black spruces were <7 feet (2.0 m) tall and 3 inches (8 cm) in diameter. Trees ranged from 3 to 37 years old, with most 31 to 33 years old. Mortality was not evident in this young black spruce stand [252].
Black spruce seedlings do not grow as quickly as hardwood sprouts [373]. On black spruce-alder sites in Ontario, for example, postfire establishment of black spruce is usually poor due to interference from faster-growing alder sprouts [22]. Field manipulations on a 1-year-old burn near Delta Junction, interior Alaska, suggested quaking aspen can outcompete black spruce for light in early postfire succession, reducing black spruce's growth rates [206]. Relative to other conifers, black spruce's slow growth is at least partially due to its relatively small seeds, which have few food reserves to support germinant growth. However, black spruce on upland sites may grow about as quickly as white spruce [113]. On 8 different-aged burns in northeastern Ontario, black spruce took longer to reach breast height (18 years) than jack pine (8 years), quaking aspen, and paper birch (7 years for both hardwoods). Time to reach breast height did not vary with either soil texture or moisture [382]. Black spruce seedlings grow poorly beneath a canopy. Zasada and others [415] report that understory black spruces take 15 to 20 years to attain 5 feet (1.5 m) in height, and it is "not uncommon" for 40-year-old black spruces under a mixedwood canopy to be <4.9 feet tall.
Poor site conditions slow growth. Black spruces on well-drained, upland sites grow tallest [113], while poor drainage [113,175] and cold climates reduce growth. Although nutrient-poor swamps and bogs are tolerated, they are not ideal habitats for black spruce growth. In northeastern Minnesota, black spruce showed progressively slower growth from the border toward the center of a swamp. Eighty-year-old trees at a swamp border averaged 60 feet (18 m) tall, but 120 feet (37 m) away—at the center of the swamp—80-year-old trees were only 20 feet (6 m) tall [243]. In Victory Basin Bog, Vermont, black spruce stringers extended from the raised bog to a nearby stream. Height and density of black spruce decreased towards the bog's center (P<00.1), although there was no corresponding difference in tree ages. Black spruces at the stream edge averaged 39 feet (12 m) tall, while those in the bog center averaged 10 feet (3 m). Age of black spruces ranged from 45 to 77 years; height was not significantly correlated with age. There was a gradient of decreased mineral content and water pH to the bog center. Dominance shifted abruptly from black spruce to speckled alder about 30 feet (10 m) from the stream edge [67]. On the Great Northern Peninsula on the northern tip of Newfoundland, black spruces took an average of 40 years to reach breast height. Tree ages ranged from 25 to 269 years; tree height and age were poorly correlated [278]. Viereck and Little [396] described growth rings of trees in northern boreal Alaska as "very narrow to almost microscopic".
Browsing can slow black spruce growth substantially, and when cone buds are eaten, it can have a "significant impact" on reproduction. Moose, hares, red squirrels, ptarmigan, and grouse are among the animals favoring black spruce twigs and buds [415]. See IMPORTANCE TO LIVESTOCK AND WILDLIFE for further details.
Comparing postlogging growth rates of layer-origin vs. seed-origin stems, layered stems were taller because of their prelogging growth. However, postlogging incremental growth was similar among the 2 groups [288].
Black spruce has a crown-stored seed bank, with seeds stored in semiserotinous cones [138,263,383].
Soil seed banking does not appear important to black spruce. Once dispersed, black spruce seeds remain viable for only a short time. In a clearcut, upland black spruce site in Ontario, portions of a seed lot that were either hand-buried or sown on the soil surface retained viability for up to 10 months, but no seeds were viable 16 months after sowing. Buried seed retained viability longer than seed sown on the soil surface (91% vs. 30% germination, respectively, 10 months after sowing) [131]. On 4 black spruce-lichen woodlands in the Northwest Territories, black spruce seed was collected from the soil, but it did not germinate in the greenhouse [186]. In New Brunswick, however, hand-sown seeds showed delayed emergence. Only 19% of black spruce seed sown on burned areas emerged in the 1st postfire year, while 25% emerged in the 2nd postfire year [366].
Seed dispersal: Wind disperses black spruce's winged seeds [4,263,396]. Since the seeds are small and lightweight [147], they may disperse 70 feet (20 m) or more from the stand edge, although most fall within the stand [197]. Most seeds disperse within about 260 feet (80 m) of their parent [375]. In logged areas, seed sources can include freshly cut slash as well as standing live or dead [5] and nearby trees. Near Ely, Minnesota, black spruce's annual seed rain averaged 3000,000 seeds/ha within a black spruce stand; 18,000 seeds/ha at 100 feet (30 m) away from the stand; and 8,000 seeds/ha at 200 feet (60 m) away. The author suggested that beyond that, seed rain would be too sparse to result in much regeneration [242]. Due to their lighter weight, black spruce seeds can disperse farther than white spruce seeds [263].
The semiserotinous cones release seeds over time [2,113,263,383,388,406,415]. Resin seals mature, second-year cones. If fire melts the resin, cones may open "in a matter of seconds" [195], although postfire dispersal is usually spread over a few years [383,388,415]. Without fire, the cones open slowly as the resin degrades. Warm air temperatures hasten this process [195]. In northeastern Ontario, unburned black spruce cones retained about 50% of their seeds after 5 years. Unburned cones tend to remain closed in cold, wet weather and open in warm, dry weather [152].
Viereck [388] reported that tremendous quantities of black spruce seed disperse during postfire years 1 and 2. In interior Alaska, the quantity of black spruce seed dispersed over 70 postfire days in a burned-over stand was 1.5 times greater than that dispersed in an adjacent unburned stand [394]. How quickly cones open and release seed is apparently related to fire temperatures: High temperatures melt cone resin and open cones quickly [395]. An initial postfire "burst" of seed rain may gradually slow to prefire levels over 2 postfire years [415]. A Saskatchewan study found that 35% of seeds from standing dead black spruces were released by postfire year 2. Only 6% of seed remained by postfire year 6 (review by [151]). Over 2 postfire years in Newfoundland, about half of black spruce's total seed rain occurred in the first 60 postfire days. Seed viability dropped quickly, from an average of 60% immediately after the fire to 20% the next spring [406]. In Minnesota, burned black spruce cones had released about 50% of their seeds within postfire year 1 and about 85% by postfire year 5 [406]. In Québec, black spruce seeds dispersed through postfire year 5. About half had dispersed by postfire year 4 [148].
Because black spruce retains its cones and the cones release seed over several years, the current year's crop is not critically important to regeneration [410]. Some report that fire will only "modestly accelerate" seed dispersal [148].
Most black spruce establishment occurs after fire, with peak occurrence during postfire years 3 to 5 [186,383]. Paired studies in Alaska and Yukon showed most black spruce establishment occurred within 10 postfire years. There was little difference in the time black spruce took to establish on thick (8-12 inches (20-30 cm)) organic soils in Alaska and thin (0-4 inches (0-10 cm)) organic soils in Yukon [206]. However, seedbed composition and organic horizon depth can influence black spruce rates of establishment and growth.
Most seeds fail to establish. On a site in Alaska, <2% of black spruce seeds that fell in postfire year 3 had produced seedlings (Zasada and others 1979 in [384]).
Rates of postfire establishment are largely determined by seed input and seedbed quality in the first few postfire years [353]. Generally, black spruce establishes best on moist lowlands where most of the moss and/or lichen layer has burned off from organic soils. The summer after winter tree harvest and spring prescribed fire in a white spruce-black spruce forest in Alberta, most spruce germinants (62%) occurred on concave microsites, with 23% on flat and 15% on elevated microsites (data for the 2 spruces were pooled). Severe fire favored spruce establishment: 43% of germinants were on plots that burned at high severity, 30% on medium-severity plots, and 27% on low-severity plots. Spruce density averaged 176,000 germinants/ha. Sixty percent of seedlings survived through the summer, but only 37% of this cohort survived through the next winter. Winter survival was greater for June germinants than for seedlings that germinated later in summer [42].
On 6 burned jack pine-black spruce sites on the Superior National Forest, Minnesota, highest black spruce establishment occurred in postfire years 2 and 3. This establishment peak was 1 or 2 years behind that of white spruce. In postfire year 1, many black spruce germinants died in a thick ash layer. Black spruce seedling survival averaged 54%, with most mortality occurring in the 1st or 2nd growing season after germination. Fires on the study sites varied in severity, with 1 to 6 inches (2.5-15 cm) of the soil organic layer burned off. Some study sites were burned under prescription and some were burned by wildfire; generally, wildfires removed more of the organic soil layer. In all cases, black spruce seedling establishment was higher on burned than on unburned soils [3,4].
In a southern boreal mixedwood in Saskatchewan, black spruce establishment was higher in mineral soil, humus (0.4-2 inches (1-5 cm) thick), or a thin layer of haircap mosses (0.4-2 inches)) than in thick haircap moss (6-8 inches (15-20 cm)), scorched haircap moss, or quaking aspen litter (2-3 inches (5-8 cm)) layers. Through the first growing season, there were no significant differences in black spruce survivorship among mineral soil, humus, and thin haircap moss seedbeds. Black spruce seedling mortality was 100% in quaking aspen litter [78].
A review suggested that on slopes, interactions of litter buildup, geomorphology, and fire may determine conifer seedling establishment and vegetation patterns. For example, black spruce generally establishes on wet slope bottoms of glaciofluvial hillslopes, while jack pine tends to occupy drier middle and top positions. Duff and organic soil layers are thicker in the black spruce stands, so when fire occurs, more ground fuels are available beneath black spruce than beneath jack pine stands. The authors concluded that duff consumption patterns were driving postfire seedling recruitment patterns on the slope bottoms and upper slopes [151].
Requirements for germination may differ from those for black spruce establishment. Although mineral seedbeds are good for germination, black spruce seedlings may grow faster on unburned organic horizons than on mineral soils ([117], review by [115]), presumably because organic horizons hold more moisture. Since black spruce seeds are small, the germinants are also small and can desiccate quickly on porous substrates [147]. However, black spruce germinants grow on a variety of substrates if the seedbed remains moist but not saturated and the site is relatively free of other vegetation [199]. Feather mosses can dry out quickly, but black spruce establishes in feather moss during wet years [129]. In a study comparing different substrates, planted black spruce seedlings grew taller on Schreber's moss or Schreber's moss-humic seedbeds than on sphagnum, decaying wood, or mineral soil seedbeds (P=0.001). The study was conducted in northeastern Ontario and northwestern Québec. Three years prior, study sites had either burned in a wildfire or been logged. Sites were classified as black spruce/bog Labrador tea/feather moss-sphagnum peatlands. Prior to disturbance, time since fire was >120 years for all sites [236].
Lowlands may support higher rates of establishment than uplands. In Alberta, harvesting and prescribed burning resulted in good black spruce seedling establishment on wet to moist low peatlands. Regeneration was "unacceptable" on fresh to moist upland sites. Before tree harvest, the community was a 100-year-old black spruce forest with a continuous feather moss-sphagnum ground layer. Burning was conducted on 29 May 1967, 2 to 3 years after selective logging. In postfire year 22, black spruce density averaged 4,162 stems/ha on unburned sites, 6,203 stems/ha on low-severity plots, and 31,563 stems/ha on moderate-severity plots. Fire severity was determined by level of peat consumption [81].
Drought was the primary cause of black spruce seedling mortality in a burned black spruce-alpine reindeer lichen woodland in Terra Nova National Park, Newfoundland. By postfire year 2, mortality of planted black spruce seedlings averaged 79%. Seedling mortality was similar on substrates that burned at low (73%) and high (76%) severities. Some plots were caged to exclude seedling browsers (voles and snowshoe hares), but there was no significant difference in mortality between caged and uncaged plots in either postfire year 1 or 2. Although mortality was initially high and the burn occurred on the southern edge of the black spruce-lichen woodland latitudinal limit, the authors predicted that black spruce's survivorship would be sufficient to replace the burned stand [293].
Interference by other species can greatly reduce black spruce's rate of establishment. In a fire chronosequence study in Terra Nova National Park, reindeer lichen substrates favored black spruce germination, but black spruce seedling establishment was negligible on that substrate. Mineral soil provided highest rates of black spruce germination (8%), seedling establishment (5%), and growth (0.4-0.8 inch (1-2 cm) at 14 months of age) [272]. Although black spruce seeds readily germinate on sphagnum, black spruce seedlings are often overtopped and engulfed by the faster-growing sphagnums [129]. Conversely, sphagnums may facilitate black spruce establishment on some sites. In the southern Brooks Range of interior Alaska, black spruce establishment was positively correlated with sphagnum (r=0.66, P=0.003). Although sphagnum covered only 15% of the soil surface, 60% of black spruce seedlings were growing in sphagnum [255].
At arctic treeline, black spruce generally establishes at higher rates than other conifers [15]. At an arctic treeline site on the southern Brooks Range, however, white spruce showed better seedling establishment than black spruce [256].
Site characteristics: Black spruce occurs mostly on cold sites, including wet lowlands and drier uplands. It grows in a variety of soils and is most common on poorly drained sites underlain with permafrost.
Climate: Black spruce grows in regions with long, cold winters and short, warm summers [383,396]. Mean annual temperatures are often below 32 °F (0 °C). Near black spruce's distributional limit at arctic treeline, annual temperatures may average 14 °F (-10 °C) [383]. Precipitation increases from west to east across black spruce's distribution. Alaska, western, and central Canada receive ≤10 inches (250 mm) of precipitation annually, while Newfoundland may average >39 inches (1,000 mm) [383].Topography and elevation: Black spruce most commonly grows on lowlands but also on uplands [129]. Lowland black spruce communities occupy river terraces and gently rolling valleys, while upland communities generally occupy low-gradient and north-facing slopes [162,225,379]. In interior Alaska, black spruce occupies poorly drained lowlands such as cold, wet flats and muskegs. It is also common on north-facing slopes within 5 miles (8 km) of major rivers and—where white spruce is absent—on upland slopes of all exposures that are more than 5 miles from major rivers [124,396]. At the southern end of its range, black spruce is mostly restricted to wet lowlands [142,375,400]. In the Great Lakes states and New England, it is most abundant on low, acidic peatlands, but it is also common on transitional sites between low peatlands and uplands [375].
Except in isolated areas of northern Minnesota and the Upper Peninsula of Michigan [375], black spruce is rare on uplands in the Great Lakes region [198,375]. In the 1830s, township surveyors on the Lower Peninsula of Michigan documented characteristics of sites with black spruce. Analyses of those data in the 1980s showed black spruce was positively associated with depressions, acidic to neutral peats, and areas with very poor drainage (P=0.1) [405].
Blacks spruce occurs from sea level to 5,000 feet (1,500 m) elevation across its range [121] but is generally found from 500 to 2,500 feet (150-760 m) [129]. In Alaska, it ranges up to 2,300 feet (700 m) elevation in Denali National Park and 3,800 feet (1,150 m) in mountainous regions of eastern Alaska [396]. Black spruce-lichen communities tend to occupy relatively high elevations [379] or latitudes. Black spruce is confined to elevations above 2,000 feet (650 m) in the northeastern United States [90].
Soils and soil moisture regimes: Poor drainage and shallow permafrost typify soils supporting black spruce [162,182,225,263,332]; black spruce is one of few conifers that tolerate such conditions [242,243,362,381,387]. However, black spruce tolerates a wide range of soil temperature and moisture regimes: It grows in in relatively warm, dry soils as well as nearly frozen, wet soils that exclude hardwoods and most other conifers [65,242,375]. Substrate moisture varies from saturated in bogs and swamps to wet on bottomlands and flats, wet to moist on lake margins, mesic on north-facing slopes, well-drained on most other slopes, and dry on drained peatlands [121,162,396].
Both lowland and upland black spruce types are most abundant on nutrient-poor soils that are poorly drained and cold [85]. Productivity in black spruce communities is lowest among boreal forest types (review by [85]). The most productive black spruce stands generally occupy south-facing slopes [379].
Although black spruce favors acidic soils, high soil or water pH may be tolerated. In Alberta, black spruce grows in bogs with extremely acidic to neutral soils (pH 4.0-7.0), but it sometimes grows in calcareous bogs with soil pH as high as 8.0 [174].
Black spruce is not well adapted to coastal fog or salt spray, so it is rare in maritime settings (review by [108]).
Permafrost tends to be continuous in black spruce's northernmost distributions, becoming discontinuous to the south [383]. The permafrost layer beneath black spruce is often shallow in boreal regions [85]. In the growing season, soils thaw to a depth of 8 to 35 inches (20-90 cm) [388]. In interior Alaska, black spruce dominates bogs with shallow permafrost [124,182,225]; permafrost tables are often as shallow as 12 inches (30 cm) [104]. Permafrost is often absent on newly deposited alluvium and south slopes and becomes discontinuous south of the Alaska Range, so black spruce is less dominant on such sites [388].
Black spruce stands typically have a thick organic mat overlying the mineral soil layer. Consequently, forest floor temperatures are lower and soil moisture content higher in black spruce muskegs than in white spruce, balsam fir, paper birch, or quaking aspen stands [380]. In Alaska, the live moss and organic soil layers may be up to 20 inches (50 cm) thick [389]. On the Laurentian Shield in Minnesota, the peat layer on black spruce sites is often 10 feet (3 m) deep, and sometimes up to 60 feet (18 m) deep [129]. In the northeastern United States, black spruce grows on peats >12 inches (30 cm) thick [40].
Black spruce grows in all soil textures [129,395] but is mostly restricted to acidic soils [91,108]. It is often reported on loams (for example, [129,205]). In the Great Lakes region, black spruce grows in coarse soils and mucks. It is common in sands, gravels, and coarse to bouldery loams [199] on lakeshores and dune ridges [400]. In northern Minnesota and southern Ontario, black spruce occurs on gravelly and bouldery loams and shallow soils over bedrock [129]. Throughout much of Canada, upland black spruce stands occur on wet to moist clays and clay loams on lowlands and long, gentle slopes. In New Brunswick, Nova Scotia, and parts of Québec, black spruce grows in sands and gravels on outwash plains, river terraces, and eskers [129]. Along a 0.6 × 9-mile (1 × 140-km) transect in southern Québec, all black spruce-lichen woodlands occurred over well-drained podzols formed in fluvial-glacial or glacial deposits [141]. White spruce is more likely than black spruce to occupy alluvial soils [332].
Plant communities: Black spruce communities are nearly ubiquitous in boreal regions of North America but have minor coverage in the Great Lakes states and the Northeast. Many factors determine plant species composition in black spruce communities, including altitude [225,388], slope, drainage, presence and thickness of permafrost, fire history, stage of succession, and canopy openness [388]. Black spruce stands establish after a stand-replacement event; usually fire, although clearcutting, disease, or insect outbreaks may also facilitate such succession.
See Appendix B for scientific names of plant taxa named in this review and for links to available FEIS reviews.
Black spruce grows in pure and mixed stands. Structure of black spruce forests often includes tall shrub and low shrub layers. Mosses and/or lichens usually dominate the ground layer, although graminoids may dominate on some sites. Trees associated with black spruce across its range include tamarack, white spruce, quaking aspen, and paper birch [129,162,395]. Bigtooth aspen is frequently associated in the southeastern portion of black spruce's range [72] and balsam poplar in the southwestern portion [162]. Quaking aspen and birches are more common in southern boreal than in northern boreal black spruce communities [383].
Tall shrubs associated with black spruce across all or most of its range include gray alder, red-osier dogwood, and various willow and birch species. Low shrubs associated with black spruce across its range include prickly rose and the ericaceous shrubs bog blueberry, black crowberry, and bog Labrador tea [383,385,395]. These tall and low shrubs can be ladder fuels during a fire. A review noted that understory diversity usually increases with time since fire and is greatest in old-growth black spruce forest undergoing gap succession [47].
The ground layer is often nearly continuous feather and/or sphagnum mosses. Splendid feather moss, Schreber's moss, juniper haircap moss, and knight's-plume moss are dominant feather mosses [395]. A review noted that in low black spruce peatlands, dominant sphagnum mosses dominant in peatlands include Magellan's sphagnum, deceptive sphagnum, and red sphagnum. Sphagnums dominant on hummocks include hairy-leaved sphagnum, Girgensohn's sphagnum, and fine sphagnum [47]. Lichen layers are sparse to nearly continuous [391] in black spruce-lichen woodlands. Reindeer lichens or green dog lichen usually dominate the ground layer; other lichen species may codominate. Feather mosses may replace lichens as postfire succession proceeds, although lichens may continue to dominate woodlands [383].
Black spruce/feather moss-lichen and black spruce-white spruce forest types occur across boreal Alaska and Canada [108]. "Primarily a Canadian forest cover type of vast extent" [111], the distribution of the Society of American Forester's (SAF) black spruce type stretches across most of Canada [111]. The SAF black spruce type is divided into 6 subtypes [90]:
1) The black spruce/feather moss forest type is most extensive; it is found in the central and southern portions of black spruce's range. Stands are well-stocked to dense spruce stands with a well-developed carpet of Schreber's moss, splendid feather moss, and/or knight's-plume moss.
2) Black spruce-dwarf shrub/Schreber's moss forests occur in the same regions, including Maine, on poor loamy sands and sandy loams. Stands are closed, with a well-developed ericaceous dwarf shrub layer. Mosses and reindeer lichens dominate the forest floor.
3) Black spruce/sphagnum forests occur throughout North America's boreal and Great Lakes regions, on very wet organic or wet mineral soils. Forests are open to closed pure black spruce stands, with a well-developed ericaceous dwarf shrub layer.
4) Black spruce-sedge forests occur across North America's boreal forest on peatlands with moving water; they are infrequent farther south. Stands are very open stands with stunted trees. Sedges, grasses, and a well-developed feather moss layer dominate the ground layer.
5) Black spruce-gray alder forests occur in the same regions, but are confined to mucky depressions where the water table is at or above the surface during the growing season. Stands are pure or mixed, occurring in areas where the water table is near the surface during the growing season. They have well-developed tall shrub and herbaceous layers.
6) Black spruce-lichen woodlands are frequent throughout black spruce's range at the forest-tundra transition zone. They have a well-developed carpet of reindeer lichens. These woodlands remain open due to cold climate.
Additionally, black spruce is codominant in SAF's balsam fir [130], black spruce-tamarack [111,145], black spruce-white-spruce [391], and black spruce-paper birch [102] forest cover types. The balsam fir type occurs in the Maritime Provinces, eastern Canada, and the northeastern and Great Lakes states on a wide variety of sites [130]. The black spruce-tamarack forest type has a similar distribution. It occupies lowland, minerotrophic streamsides and peat bogs [145]. Tamarack becomes dominant on very wet, nutrient-poor sites [206]. Black spruce-white spruce woodland or forest types occur from Alaska and across Canada to the Hudson Bay. Black spruce-tamarack sites are typically near latitudinal or elevational treelines. Sometimes, these sites have characteristics intermediate to those favored by tamarack (low and acidic) and those favored by spruces (upper floodplain terraces and bases of south slopes) [391]. The black spruce-paper birch forest type occurs in intermittent, small patches in Alaska and Yukon. It is a seral type that occurs after severe ground fire exposes mineral soil. It occupies loess or glacial till slopes with shallow permafrost [102].
See the Fire Regime Table for a list of plant communities in which black spruce may occur and information on the FIRE REGIMES associated with those communities. More detailed descriptions of black spruce communities follow by region.
Alaska: Black spruce dominates or codominates most Alaskan taiga landscapes [206]; black spruce is the most common forest type in the state [85]. It has dominated Alaska's boreal region for the past 5,500 years [265]. Black spruce communities presently occupy 39% to 44% of interior Alaska [69]. At the landscape level, Alaskan black spruce communities form mosaics with quaking aspen-birch, white spruce, and mixedwood (spruce-hardwood) stands. Black spruce generally occupies the most poorly drained, coldest portions of these mosaics (see Site characteristics). White spruce and hardwoods generally occupy relatively warm sites, and balsam poplar and black cottonwood dominate floodplains of major rivers [388].Lowland black spruce communities are mostly wetlands, while upland black spruce communities are drier [386]. Lowland black spruce forests are abundant in interior Alaska [122,124] but sporadic on the southern coast (Copper River Basin and Cook Inlet lowlands). Coastal black spruce forests are open and interspersed with shrub tundra [279].
Several species or genera are common in many Alaskan black spruce types including quaking aspen, paper birch, white spruce, and tamarack in the overstory; willows and ericaceous shrubs in the shrub layer; and cottongrasses, feather mosses, sphagnum mosses, and reindeer lichens in the ground layer [124,162,386]. Black spruce branches are often draped with arboreal lichens including Fremont's horsehair lichen and old man's beard [263].
An upland black spruce forest.Foote [122,124] identified several black spruce forest types of interior Alaska. She noted these types might be difficult to distinguish in early postfire succession, but could usually be distinguished from one another by postfire year 50 [124].
Black spruce dominates some riparian areas of interior Alaska. In Kobuk Valley National Park, it dominates poorly drained lowland and some slope forests of the Salmon River valley. Black spruce stands generally dominate river bends where fine-textured sediments are exposed, while balsam poplar or white spruce dominate coarse-textured soils along the riverbank. Black spruce-reindeer lichen woodlands occur on sandy ridges, knolls, and bluffs. Dwarf black spruces have scattered occurrence in heathlands [282]. Along the Kuskokwim River, open black spruce-quaking aspen forests occupy upper terraces, while black spruce/sphagnum muskegs occupy low terraces [99]. On the Tanana River floodplain, open white spruce-black spruce stands were transitional between the active floodplain and upper, older terraces. Canopy cover ranged from 25% to 50%. These stands were 150 to 250 years old and uneven-aged. Open (40%-60% canopy cover) black spruce/bog Labrador tea stands were found on upper terraces of the active floodplain. Both mixed spruce and black spruce bog types were always underlain with permafrost, frequently with a shallow active layer. Black spruce bogs occupied the uppermost, oldest terraces. These poorly drained areas originated on sites where the upper permafrost layer was melting [392].
Black spruce does not always codominate mixed-conifer forests. It is a minor species in many tamarack bogs [101]. In interior Alaska, it is usually a minor component of white spruce forests. In white spruce communities, it is most common on well-drained uplands during early postfire succession [162].
Black spruce is generally a minor type in southern Alaska. It occurs over scattered pockets of permafrost, mainly on muskegs of the Kenai Lowlands. An open to closed black spruce/bunchberry-mountain cranberry/lichen community type has been identified there [329]. Black spruce dominates some hills and ridges of the Ahklun Mountains, and it is the dominant forest type in the Koskokwin Mountains [279]. Open black spruce forests are interspersed with shrub tundra in the Copper River Basin and on Cook Inlet lowlands [279].
Great Lakes: Black spruce dominates some cold forests and wooded bogs of the Great Lakes region. It is common in mixed-conifer and occurs in some maple-beech-birch communities. It often codominates with jack pine in mixed-conifer communities [7]. In the Boundary Waters Canoe Area of Michigan, a black spruce-paper birch-jack pine community was noted on Fishhook Island, and black spruce was a component of a red-maple-balsam fir-eastern white pine community near Hegman Lake [133]. Jack pine-black spruce and black spruce-jack pine communities of Boundary Waters Canoe Area generally differ in understory structure and composition: The jack pine-black spruce community typically has well-developed shrub and herb layers. The black spruce-jack pine community generally lacks those layers but has a feather moss layer that covers nearly 100% of the ground. Both communities occur on southerly, low and midslopes with poorly drained soils, with jack pine becoming less important with time since fire. Black spruce is occasional to important in red maple-quaking aspen-paper birch, eastern white pine, and northern whitecedar communities of the Boundary Waters Canoe Area. It is a minor species in red spruce communities [303].
Four black spruce forest associations are described for Isle Royale National Park, Michigan. They include black spruce/Schreber's moss, jack pine-black spruce/low sweet blueberry/Schreber's moss, black spruce/speckled alder/peatmoss (sphagnum and calliergon mosses) rich swamp, and black spruce/bog Labrador tea/sphagnum poor swamp. These forests are uncommon in the Park but also occur in northern Michigan and northeastern Minnesota. The black spruce/bog Labrador tea forest also occurs in Wisconsin. Canopies of the black spruce/Schreber's moss forest are typically closed (60%-90% canopy cover), while canopies of the jack pine-black spruce forest are open (~60%), with black spruce in the subcanopy. The black spruce/speckled alder forest occurs in wet depressions. It has an open canopy (30%-40%) and a tall shrub layer (20%-40%). Short and dwarf shrubs are sparse. The black spruce/bog Labrador tea swamp forest also occurs in wet depressions, with an open canopy (20%-50%) and a subcanopy of tall shrubs (5%-30%) and black spruce (1%-25%). Black spruce is sometimes codominant in northern whitecedar/speckled alder, jack pine-eastern white pine, and tamarack rich swamp forests of Isle Royale National Park [365].
Black spruce/sphagnum bogs occur on lowlands of northern Minnesota [279] and Michigan. Shrubby black spruce peatlands or black spruce-tamarack swamps dominate sandy glacial lake plains [7]. In Voyageurs National Park, Michigan, black spruce/speckled alder and black spruce/laurel communities occurred on wet, nutrient-poor lowlands. The overstory was nearly pure in black spruce/speckled alder, but the herb layer was often diverse. Black spruce/laurel ecotypes were more open and less diverse, possibly because nutrient levels were very low. Black spruce was an associated to dominant species of red pine-eastern white pine/twinflower and balsam fir-spruce-paper birch/clubmoss ecotypes on drier, richer soils [226].
Mixed forests of this region may have an important black spruce component. Kuchler [224] described a tamarack-black spruce-northern whitecedar conifer bog type that had scattered occurrences in the northern Great Lakes region, New York, and New England. In the mid-1850s in northwestern Wisconsin, surveyors recorded a mosaic of wet sedge meadows interspersed with small patches of lowland tamarack-black spruce woodlands [399]. In northeastern Wisconsin and Michigan's Upper Peninsula, black spruce is successionally dominant in logged or logged-and-burned eastern hemlock-red maple-sugar maple and eastern hemlock-northern whitecedar habitat types [83].
Conifer swamps with black spruce, northern whitecedar, tamarack, and/or eastern hemlock are scattered throughout Wisconsin [86,223]. Tamarack-black spruce communities occur as open bogs, swamps, or closed wet forests in northern Wisconsin. Overstories vary from nearly pure tamarack to nearly pure black spruce. Black spruce usually dominates paludified lake basins completely filled with peat, while tamarack usually dominates where bog mats are still advancing into open water [86].
Northeast: Black spruce dominates some conifer bogs of the Northeast. Dammam and French [91] describe 2 black spruce forest bog community types within this region: black spruce/Magellan's sphagnum of New England and northern Maine and black spruce/threeseeded sedge of New England. Stand structure in Magellan's sphagnum types range from open to closed and dense, with a well-developed sphagnum carpet. The shrub component decreases with increasing overstory density. Ericaceous thickets dominated by highbush blueberry, swamp azalea, bog Labrador tea, and/or catberry may succeed to this forest type. The black spruce/threeseeded sedge type borders northern hardwood or spruce forests; balsam fir may codominate in the overstory [91]. Black spruce also occurs in mixed-conifer, mixedwood, and heathland communities. Its importance decreases in the southern limits of its distribution in this region.
In Maine, black spruce dominates some late-successional conifer communities. Red spruce and balsam fir often cooccur, especially in canopy gaps and on forest edges [228]. In Acadia National Park, black spruce dominates some conifer/heathland communities and occurs in subboreal mixed-conifer forests that are transitional to the boreal spruce-fir forests of Québec. A black spruce/sheep-laurel woodland occurs on rocky sites, and a black spruce/highbush blueberry-black huckleberry/sphagnum woodland occurs in bogs. Black spruce is an important component of red maple woodland swamps and mixed-conifer forests with red spruce, eastern white pine, tamarack, and/or northern whitecedar [259].
In the Adirondack Mountains of New York, black spruce dominates some conifer and mixedwood forests. It replaces red spruce as the dominant tree at high elevations [163,328] (≥1,200 feet (360 m)) [163]. In midelevations of the Adirondack Mountains, black spruce dominates poor fens, while red spruce dominates rich fens by streams [330]. A balsam fir-black spruce/bunchberry/splendid feather moss forest association occurs in the Adirondack and White mountains on very strongly acid soils. Eastern white pine often dominates after fire until black spruce replaces it successionally [163]. On soils that are only seasonally moist, black spruce sometimes dominates mixedwoods with yellow birch, black cherry, and eastern hemlock. These forests occur on flat lowlands or border swamps, lakes, or streams [328]. Above 3,500 feet (1,000 m) in the Adirondack Mountains, black spruce grows as krummholz in balsam fir alpine dwarf woodlands. A black spruce-eastern hemlock talus community occurs in the ice caves (icy rock crevices) of Shawangunk Ridge [328].
Black spruce bogs and swamps are scattered throughout New York. Black spruce-tamarack/sphagnum bogs occur on acidic peatlands in cool, poorly drained depressions. The canopy is open to closed (50%-90%), and the shrub layer is composed of ericaceous species. Stringers of black spruce, often with tamarack, are interspersed with low sphagnum peatlands. The trees are usually dwarfed. In northern and central New York, black spruce is a component of northern whitecedar swamps [328].
In the White Mountains of New Hampshire, black spruce is an associated species of high-elevation balsam fir-quaking aspen forests. Red spruce dominates at low elevations [327]. On the White Mountain National Forest, dwarf black spruce and tamarack cooccur on shrub islands within acidic fens and on small (<2.0 acre (0.8 ha)) forest seeps [336].
Black spruce is occasional in Mud Pond Bog, New Hampshire. Red maple dominates the swampland area of Mud Pond Bog, but black spruce is a component of the swamp. Scattered black spruce trees grow in leatherleaf/sphagnum and black huckleberry-highbush blueberry heathlands, and black spruce grows in dwarf form in sheep-laurel-threeseeded sedge heathlands [100].
In the Allegheny Mountains of northeastern Pennsylvania, black spruce occurs in the transitional zone between oak-hickory and northern mixedwood ecosystems. An eastern hemlock-black spruce bog community was noted at 2,100 feet (640 m) in a flat, poorly drained area. The canopy was so closed that most shrubs were excluded, and the ground layer was thick sphagnum. Woody debris was substantial and the water table was near ground level; often, standing pools of water formed in tip-up pits. A black spruce/tamarack/black highbush blueberry-highbush blueberry/sphagnum bog community was noted at 1,900 feet (580 m) [98].
In New Jersey, where black spruce reaches its lower latitudinal limit, black spruce-tamarack swamps are occasional in lowlands. Black spruce is a component of highbush blueberry bogs [338]. A red maple-black spruce-highbush blueberry palustrine woodland is described in the New Jersey portion of Delaware Water Gap National Recreation Area. The woodland occurs in isolated pockets of upland depressions, within a larger wetland matrix. The woodland soil is very poorly drained and sometimes overlain with muck or peat [322].
Western Canada: In British Columbia and Alberta, black spruce associates with white spruce, Rocky Mountain lodgepole pine (hereafter, lodgepole pine), subalpine fir, and balsam poplar on upland sites. It occurs mostly in pure stands in bogs, although tamarack may be a minor tree. The ground layer is composed of feather and/or sphagnum mosses [174]. In interior portions of the Prince Rupert Forest Region, British Columbia, black spruce/peatmoss communities typically occur in frost-pocket depressions where the peat mat has grown over a pond or lake. Sites range from very acidic bogs to neutral fens, with canopies ranging from very open to closed [153].
In Yukon, black spruce is an indicator of permafrost sites. Black spruce/bog Labrador tea/splendid feather moss forests are multilayered, with grayleaf willow in the tall shrub and ericaceous species in the low shrub layer [305]. Open black spruce-tamarack/bog blueberry/lichen taiga occurs in the foothills of the Richardson Mountains. The shrub canopy is closed. Slopes are gentle and have poor drainage, with permafrost at depths of 13 to 26 inches (33-65 cm) [356].
In the Northwest Territories east of Great Slave Lake, black spruce codominates open parklands with jack pine, white spruce, and paper birch. Ericaceous species (crowberry, Labrador tea, and blueberry spp.) dominate the shrub layer, and lichens (snow, cetraria, and reindeer lichens) dominate the ground layer. Black spruce dominates open, forested peatlands; tamarack is infrequently associated. Plateaus are generally treeless lichen tundra [188].
Central and eastern Canada: In the central portion of black spruce's boreal distribution, jack pine displaces lodgepole pine as the codominant [106]. Black spruce tends to grow on wet lowlands, while jack pine grows on dry uplands. With accumulation of soil organic material due to fire exclusion or long fire-return intervals, black spruce may eventually replace jack pine successionally on uplands [404].
In eastern Canada, black spruce tends to dominate mixed-conifer and mixedwood forests on poorly drained sites. In Ontario, it dominates poorly drained lowlands and codominates with white spruce, quaking aspen, and/or paper birch on uplands. It codominates with jack pine on some sand plains and well-drained, shallow soils [92]. In Quetico Provincial Park, Ontario, jack pine, black spruce, and balsam fir cooccurred in a nearly even-aged stand. Trees ranged from 40 to 69 years old. Jack pine dominated the overstory; black spruce the midstory; and balsam fir the understory. The dense balsam fir understory prevented further conifer establishment. In a 160-year-old stand, black spruce dominated the canopy, with white spruce and jack pine codominating. Paper birch and sugar maple were establishing in the canopy, with the conifers "in the process of breaking up" successionally. Black spruce regeneration was growing slowly, likely due to shade cast by the hardwoods [93]. A mosaic of black spruce-red spruce-balsam spruce and yellow birch-paper birch-red maple occurs on lowland forests in New Brunswick. Black spruce forest occupies poorly drained areas, and the hardwood forest occupies well-drained sites at the periphery of poorly drained sites [402]. In Newfoundland, the black spruce/sheep-laurel forest type is very open (<20% canopy cover), with a ground layer of feather mosses and reindeer lichens. Speckled alder-black spruce swamps occur in mucks with an organic layer >6 inches (15 cm) thick [89].
In Nova Scotia, black spruce bogs occur in a matrix of shrublands and open water. Stunted black spruce are scattered within rocky, black huckleberry-broom crowberry heathlands in southern Nova Scotia [361].
Black spruce dominance increases with latitude in eastern boreal forests. In eastern Québec, black spruce increasingly replaces balsam fir as permafrost thickens [94]. Krummholz black spruce-reindeer lichen woodlands and forests grow at the boreal-arctic treeline interface in Québec. In one study, black spruce occurred as scattered stands on sites that last burned <600 years prior, while reindeer lichens were the primary cover on soils that had not burned for >1,000 years [313].Black spruce is found in all stages of boreal forest succession [87]. Its shade tolerance is intermediate [87]: It grows in open bogs and woodlands [87] as well as in closed-canopy forests [390]. It typically seeds in promptly after fire (see Seed dispersal and Plant response to fire). Although quaking aspen, paper birch, and shrubs frequently sprout or colonize after fire in black spruce types, black spruce usually regains dominance [390] in 90 postfire years or less [383]. However, if fire returns before the black spruce stand has produced many cones (around 30 years old [395]), the site may convert to a hardwood or shrubfield type [162]. The presence of white spruce in nearby, unburned stands increases the change of white spruce becoming codominant with black spruce after fire [203,204,207,383]. Horton and Lees [174] speculated that in the long-term absence of fire in Alberta, black spruce/feather moss bogs would succeed to white spruce-black spruce or subalpine fir types. However, they point out that "fire generally does occur, preventing this succession" [174].
Many factors affect postfire trajectories in black spruce ecosystems, including prefire plant community composition, fire severity, presence of permafrost, and postfire weather [53,203,204,383]. The patchy burn patterns typical of black spruce communities perpetuate numerous seral communities. A review of postfire succession in boreal black spruce/feather moss forest types found this general pattern [383]:
1) Conifer seedling-herb stage, postfire years 1 to 4: black spruce seedlings and common liverwort-fire moss mats often dominate. Ericaceous shrubs and willows sprout in areas that burned at low to moderate severity. Plant cover may increase from 0% to 40% or 50% during this stage.
2) Shrub stage, postfire years 6 to 25: Shrubs establish and/or continue to grow, gaining dominance as cover of mat-forming and herbaceous species decreases.
3) Young tree stage, postfire years 25 to 30: Black spruce gains dominance and may be very dense. Tree density (all species) may exceed 4,000 saplings/ha, with up to 12,000 seedlings/ha. Willows and alders begin to thin, but ericaceous shrubs and paper birch continue to gain cover. Cover of feather mosses and other mosses also increases. Thawed permafrost layers may refreeze as the soil organic layer increases.
4) Mature tree stage, postfire years 60+: Around postfire year 60 to 90, black spruce tends to form closed stands. It self-thins to about 1,700 trees/ha around postfire year 100. Stands have layered branches and are often clumped; shrubs occupy spaces between black spruce clumps. Lichen cover continues to decline.
The degree to which fire burns off organic soil layers greatly influences postfire succession and plant community composition in black spruce communities [207]. In general, intact soil organic layers tend to prolong a graminoid- or shrub-dominated successional phase after fire, while exposed mineral soil promotes postfire establishment of hardwood trees [383]. Hollingsworth (2008 cited in [65]) remarked that in black spruce ecosystems, moisture content of the soil organic layer during fire is an important driver of succession afterwards: "Unless conditions are dry enough to allow the fire to burn down to the organic layer, chances are the system is going to regenerate exactly how it was before the fire". Black spruce is most likely to replace itself successionally after ground fires that leave some organic layers unburned, whereas hardwood trees are most likely to establish with black spruce if they were present before fire and/or if soils are burned down to either shallow organic or mineral layers [203,204,207]. Viereck [383] reported that in Alaska and northern Canada, shrub cover is usually sparse after fires that burn down to mineral soil, but such fires prepare good seed- and sporebeds for black spruce, mosses, and lichens. Postfire sprouting of shrubs is most likely when organic soil layers are not entirely consumed [383].
After severe fire, hardwood trees may dominate for 50 to 80 postfire years before black spruce regains dominance. If hardwoods were on site before low- to moderate-severity fire, postfire sprouting of hardwood trees may prolong the hardwood stage for 60 to 90 postfire years [383]. In the Great Lakes states, hardwoods may replace black spruce on uplands [243]. Some conjecture that black spruce types may succeed to hardwood types following either a fire severe enough to kill seed stored in black spruce crowns or a recurrence of fire before black spruce has matured enough to produce cones [263,388]. See Fire Management Considerations for further discussion on the effects of very short fire-return intervals on black spruce.
Viereck [383] suggested that a quaking aspen community with a black spruce understory develops after a severe fire burns organic alluvium down to mineral soil and quaking aspen and black spruce seedlings establish around the same time. Black spruce likely replaces quaking aspen successionally on these sites unless fire returns within the lifespan of quaking aspen [383], approximately 100 years [196].
Frequent fires (<100-year intervals) often convert fir or spruce-fir forests to spruce forests. In black spruce-balsam fir forests, balsam fir recovers more slowly after fire than black spruce. Like black spruce, it has thin bark and is easily killed, but unlike black spruce, it has nonserotinous cones that experience high seed mortality during fire (review by [137]). After fire, a balsam fir forest with a black spruce seed source either on site or nearby may convert to black spruce [89]. Without fire, balsam fir may replace black spruce on some sites [383]. In subboreal and boreal regions, it is likely that fir-dominated communities will succeed to black spruce or other later-seral conifers, such as tamarack, balsam fir, and northern whitecedar, if late-seral conifers were present before fire (review by [137]).
In southeastern Canada and the northeastern United States, balsam fir and northern whitecedar are more shade tolerant than black spruce and tend to replace it successionally under long fire-return intervals [40,87]. However, black spruce may remain codominant with balsam fir or maintain a "strong presence" [87].
Where jack pine is present before fire, it may establish in larger numbers than black spruce after fire because its cones are totally serotinous (review by [383]). In jack pine communities on the Superior National Forest, Michigan, black spruce advanced regeneration usually gained dominance over jack pine after blowdowns, while jack pine regained dominance after fires [88]. In the Great Lakes states, black spruce often establishes beneath the canopies of pine and mixedwood communities [88]. In northeastern Minnesota, where black spruce often codominates with jack pine, black spruce may replace jack pine successionally on sites that experience long periods between fires or other stand-replacing disturbances [243].
Generally, a site must remain cold for black spruce to maintain dominance (see Site characteristics). Black spruce usually replaces white spruce successionally on permafrost sites [381,387], while white spruce usually replaces black spruce on relatively warm, dry sites. On alluvial sites, periodic fires help prevent development of a permafrost layer, which may prevent succession of white spruce to black spruce [15]. Near rivers, black spruce may replace white spruce on old terraces as the soil organic layer builds up and the permafrost table rises; this may occur on upland sites as well (review by [383]). By the Tanana River, Alaska, black spruce presence was positively correlated with backswamp and other poorly drained permafrost areas and with areas that burned <200 years prior. White spruce was positively correlated with meander belts (P=0.05 for all variables) [274].
Fires that reduce permafrost layers may result in lowered black spruce density or a type shift to hardwoods. Permafrost renders the site wetter and therefore, less likely to experience severe ground fire in most years [207]. However, severe ground fires occur in extreme fire years. When the insulating organic layer is reduced or removed by such fire, the active layer above permafrost often increases [171,212,408]. On some such sites, soils no longer freeze completely in winter, so they drain intermittently and dry out. Plant community composition shifts in response to these drier conditions. While wet soils over shallow permafrost favor black spruce, soils with deeper active layers favor quaking aspen, birches, and alders [171]. This hydrologic-thermal regime is a primary factor controlling plant succession in taiga underlain with permafrost [378].
Tree species composition and abundance may show only short-term change after fires in boreal mixedwoods. On 3 recently burned sites in central Saskatchewan and 1 in central Québec, density of quaking aspen sprouts was greater than densities of black spruce and jack pine seedlings, but relative abundance of the 3 species became similar as quaking aspen sprouts thinned over time. For all 3 species, there was a significant, positive relationship between prefire basal area of mature trees and basal area of postfire regeneration (P=0.05). The authors concluded that for these species, there was little change in pre- and postfire species composition. In Saskatchewan, the prefire forests ranged from 50 to 90 years old and burned in May or June. In Québec, the prefire forest was about 40 years old and burned in early summer [146].
Black spruce may invade the borders of open shrub or herbaceous bogs. In Matanuska Valley near Anchorage, for example, black spruce invaded a bog rosemary-sweetgale-arctic dwarf birch-sphagnum bog [158]. Where permafrost is near the soil surface, an open sphagnum bog may develop into a mosaic of sphagnum bog and black spruce woodland [15]. Pioneering black spruce and tamarack frequently invade sedge mats of filled-lake bogs. In time, they may form stable swamps [129]. In the Great Lakes states, black spruce is usually a late-seral species in bogs and swamps [243]. However, as the peat soil is gradually elevated by the accumulation of organic matter and the fertility of the site improves, balsam fir and northern whitecedar may eventually replace black spruce and tamarack [129,243]. At broad scales, black spruce bogs tend to become more homogenized, less productive, and have smaller trees as paludification progresses [160].
Insects: Insect outbreaks—especially eastern spruce budworm outbreaks—affect successional pathways throughout black spruce's distribution. Since the settlement period, eastern spruce budworm outbreaks have occurred in 40- to 60-year cycles. Prior to the 1800s, they were apparently less frequent and affected less of the landscape [228]. Unlike fire, which kills all or most overstory conifers, eastern spruce budworm outbreaks tend to reduce balsam fir cover over that of black spruce or white spruce [120,216,228]. Among eastern spruces and firs, black spruce is considered the least susceptible to eastern spruce budworm attacks, followed by red spruce, white spruce, and balsam fir, which is most susceptible (review by [270]). Since hardwood species are not attacked, they are favored over all susceptible conifers. However, not all susceptible conifers die, so recovering stands become uneven-aged as black spruce and other conifers establish near recovering conifers [47,94]. In south-central Québec, most black spruce mortality during eastern spruce budworm outbreaks occurred in small, suppressed trees, with mortality increasing with stand density (P<0.001) [261].
A review noted that annually, eastern spruce budworm outbreaks affect succession over a larger area than fire. After eastern spruce budworm attacks, tree mortality and consequent gap succession increased with time since fire. In eastern Canada, increasing postattack abundance of balsam fir was strongly correlated with time since fire [47].
Multiple disturbances over a short time may result in a type shift from black spruce forest to shrubland or woodland. In eastern Québec, black spruce/feather moss stands defoliated by eastern spruce budworm may take 20 years to recover. If fire occurs before then, the site may convert to open black spruce-lichen woodlands [348]. In southeastern Québec, a black spruce/feather moss forest was subject to staggered logging from 1940 to 1980; eastern spruce budworm outbreaks in the late 1970s and mid-1980s; and a wildfire in 1991. Although eastern spruce budworms preferred balsam firs and white spruces, black spruces in the region also showed heavy defoliation or mortality during the outbreaks, and postlogging black spruce regeneration was only beginning to bear cones when the outbreaks occurred. The combined result of these disturbances was a loss of seed-bearing black spruce and consequently, poor postfire regeneration. In postfire year 4, the area was an ericaceous shrub-lichen parkland with few black spruce seedlings [314].
Gap succession: Insect outbreaks, asynchronous mortality of individual trees, windthrow, fungi, eastern dwarf mistletoe infection, and paludification can create gaps in black spruce communities. On a fine scale (≤7 feet (2 m)), this can lead to open patches [160]. In gap succession, black spruce generally remains dominant if it was dominant before the gap-creating disturbance [47]. In in 1930s in northern Minnesota, LeBarron [242] observed uneven-aged black spruce stands in open peatlands and old forests. He attributed this to black spruce seedlings "filling in" canopy gaps where mature black spruces had died [242]. Gaps resulting from windthrow and root-rot fungi are often smaller than those resulting from insect outbreaks [47]. In the Abitibi region of east-central Ontario and southwestern Québec, gaps in boreal black spruce forests increased with time since fire (P=0.05). Eastern dwarf mistletoe might have accelerated the transformation of even-aged to uneven-aged stands. Infection rates usually increased with time since fire [243]. See Fire Management Considerations for information on controlling eastern dwarf mistletoe in black spruce stands.
Effects of climate change on succession: Advancement or retreat of black spruce at arctic treeline is controlled primarily by climate. Black spruce woodlands shift northward in warm periods, while tundra shifts southward during cold periods. The last cold shift spanned approximately 500 to 100 years BP. Upheaval of permafrost aggregates in open peatlands can favor black spruce establishment and formation of black spruce krummholz or forest stands as the aggregates dry [313]. See Fire and climate change for further information on this topic.
Regional studies: Examples of succession in black spruce communities follow by region. Alaska: Black spruce is present in all stages of postfire succession in Alaska, although it does not regain dominance for several postfire decades. In interior Alaska, the most common pattern of postfire succession in black spruce forests is rapid replacement of a mature black spruce stand by a dense, young black spruce stand. Stands thin with time since fire, eventually forming open woodlands or scattered muskegs [388]. Throughout much of Alaska, quaking aspen and paper birch dominate seral stands on relatively warm sites. Hardwood stands begin to break up around postfire year 90, when black spruce becomes dominant. Since fires usually occur every 100 years or less, midseral communities codominated by hardwoods and black spruce are widespread [124].Foote [122] noted that in burned black spruce forest communities on the Tanana highlands of interior Alaska, black spruce seedlings were apparent by postfire years 1 to 5, but willow or ericaceous shrubs dominated until about postfire year 25. Hardwoods and small black spruces dominated the canopy from postfire years 26 to 50, after which a dense black spruce/Schreber's moss stage developed. The canopy thinned around postfire year 100. She noted that black spruce-quaking aspen-paper birch/bluejoint reedgrass and quaking aspen-black spruce/red-osier dogwood community types required frequent fire (≤100 years) to maintain the hardwood component. Of 90 black spruce stands surveyed, most were in early postfire succession (<26 years old) [122].
Table 1. Ages and number of black spruce stands found on the Tanana highlands, interior Alaska [122] Age (years) Number of stands represented 0 3 1-5 31 6-25 18 26-50 14 51-100 13 >100 11In a follow-up study, Foote [124] surveyed 130 black spruce or white spruce stands that were 1 month to 200 years old. Results of that study are discussed in Plant response to fire. See her Research Paper for general information on postfire succession in black spruce communities of interior Alaska and details about her studies on the Tanana highlands [124].
In interior Alaska, patterns of early seedling establishment strongly dictate community composition of black spruce types for at least 2 or 3 postfire decades [206]. Fruticose lichens often colonize dry soils, developing a nearly continuous cover that can delay black spruce establishment. Dry sites eventually succeed to black spruce-lichen woodlands. Feather mosses are most likely to colonize moist sites, which generally succeed to closed-canopy black spruce/feather moss forests [383]. In wildfire-burned black spruce stands in interior Alaska, severe fires favored forbs with wind-dispersed seeds, such as fireweed. Mosses, liverworts, and lichens were most common on moist sites; those groundlayer components were little impacted by moderate-severity fires but declined after severe fires. Deciduous and evergreen shrub cover declined after fire, with evergreen, ericaceous shrubs such as black crowberry decreasing with increasing fire severity (P≤0.03 for all variables) [53]. Postfire species composition in black spruce types appeared highly correlated with fire severity and site moisture 1 year after wildfires in summer 2004. Wet to moist sites were significantly more likely to support residual sprouting and nonvascular plants than dry sites (n=90 sites total). On the 14 sites for which there were prefire data, dry sites and those that had high-severity fire (burned to mineral soil) showed the greatest changes from prefire species composition [173].
Fungal species in black spruce communities also undergo postfire succession. A chronosequence study near Delta Junction found fires did not appreciably reduce abundance of vesicular-arbuscular mycorrhizal fungi. However, ecotmychorrizal fungi required up to 15 years to return to prefire levels. As postfire fungal succession progressed, ecotmychorrizal fungi replaced vesicular-arbuscular mycorrhizal fungi [371].
Several papers are available to help predict successional patterns in black spruce ecosystems of interior Alaska:Northeast: Fire histories and consequent patterns of succession were not well documented for black spruce ecosystems of Maine. Experts suggest that fires occurring early in the growing season or during drought years apparently favor quaking aspen and paper birch, which sprout, over black spruce. After early-season fire, succession to a black spruce-balsam fir overstory may be delayed for as long as 120 years. It is likely that successional patterns in black spruce forests of Maine are similar to those in black spruce forests of southwestern Québec [228], which are discussed in the Eastern Canada section below.
Little information was available on successional patterns in black spruce forests and mires of the Northeast (as of 2014). In a 94-year-old catberry-highbush blueberry mire in central New York, black spruce had the greatest density and basal area of canopy trees; black spruce in the canopy averaged 24 years old. The mire developed after a stand-replacement wildfire [244].
Western Canada: Black spruce tends to replace jack pine and lodgepole pine successionally on relatively dry sites in western Canada [129]. In central-interior British Columbia, black spruce dominated some mature (41-140 years) and old-growth (>140 years) stands. An even-aged lodgepole pine cohort that established after fire dominated most stands <41 years old [96].
A fire chronosequence study on drumlins (compact glacial till forming mounds or low hills) near Great Slave Lake, Northwest Territories, illustrates successional phases of black spruce communities in western boreal Canada. A globose haircap moss phase occurred from postfire years 1 to 20; a reindeer lichen phase from postfire years 21 to about 60; an open-canopy black spruce/Easter snow lichen phase from about postfire years 61 to 130; and a closed-canopy black spruce/splendid feather moss-Schreber's moss phase after about postfire year 130. Succession to the feather moss stage was rare, because fire usually set succession back before then (n=19 sites and 70 plots) [271].
Near Watson Lake, Yukon, succession was studied after stand-replacing wildfires in black spruce-lodgepole pine stands (n=39 stands). In stands that were <30 years old before they burned, black spruce and lodgepole pine had significantly lower rates of early postfire establishment than in stands that were older before they burned (P<0.009). On sites where stands were >80 years old before they burned, black spruce and lodgepole pine densities were significantly related with their prefire basal areas (P≤0.03). Quaking aspen densities did not differ with stand age prior to fire (P<0.77) [206].
Open boreal bogs and marshes may eventually succeed to black spruce bogs. However, because paludification takes centuries to millennia, direct evidence of this is lacking. Moss [292] suggested that in Alberta, "circumstantial evidence...indicates a natural succession from (sedge) marsh, through tamarack swamp, to Sphagnum bog and bog forest dominated by black spruce".
On upland sites across boreal Canada, white spruce may replace black spruce with long fire-return intervals; however, long fire-free periods rarely occur. Typically, upland sites have fire-return intervals short enough to favor black spruce, jack pine, and/or lodgepole pine. Rowe [332] stated that in black spruce's southern distribution, several fires per century may be needed to prevent succession to white spruce, while at the boreal forest-arctic treeline, a fire every few centuries may prevent such succession.
Eastern Canada: The general pattern of succession in conifer forests of this region is early dominance by black spruce, with successional replacement by balsam fir when fire-return intervals are long. If jack pine cooccurs in the overstory, it may dominate or codominate with black spruce in early postfire succession, particularly after severe fire. Sprouting ericaceous shrubs may also dominate early postfire succession in black spruce communities. A chronosequence study in Terra Nova National Park found sheep-laurel dominated burned black spruce sites until about postfire year 60, with 50% to 90% cover from postfire years 1 to 60. Black spruce cover was negligible until postfire year 20, followed by a slow increase, with black spruce cover surpassing that of sheep-laurel after about postfire year 60. Lichen cover increased at a rate similar to that of black spruce [272]. A study in south-central Québec found that in 2,000 miles² (5,000 km²) of black spruce-jack pine-paper birch/feather moss forest, roughly 10% of the landscape was in early postfire succession (0-30 years). Young forests (31-80 years) comprised <1% of the landscape, while mature forests (81-150 years) accounted for 38%. Most (>51%) was old growth (>150 years) [38]. To date (2014), most postfire successional studies in this region were conducted in Québec.
Sheep-laurel heath, 27 years after a fire in a black spruce forest. Photo taken near Terra Nova National Park, Newfoundland, by A. U. Mallik.Relatively long fire-return intervals favor black spruce over jack pine. A model developed for poorly drained black spruce-jack pine boreal forests east of James Bay predicted that a 47-year fire-return interval favored successional replacement of black spruce by jack pine. However, continued dominance of black spruce was predicted with 211- to 270-year fire-return intervals [241]. On 2 sites in Québec that burned 38 and 43 years previously, jack pine had replaced black spruce successionally as the dominant tree species. The authors observed that while black spruce did not "substantially regenerate" in these early postfire decades, jack pine density "noticeably increased in most cases" [235].
In a fire history study in northeastern Québec, black spruce tended to dominate either early postfire communities where it dominated prior to fire or late-seral communities that had not burned for >175 years. Balsam fir often codominated the late-seral stands [94]. Time-series aerial photos of burned sites, taken near the Gulf of St Lawrence in 1930, 1965, and 1987, show 3 patterns of postfire succession. In 1 pattern, black spruce was dominant in early postfire succession, and remained so through late postfire succession. In the other 2 patterns, hardwoods dominated early seres, but either black spruce or balsam fir successionally replaced the hardwoods. Sites where black spruce was dominant throughout successional seres were positively associated with well-drained, thin tills or imperfectly drained tills, while sites that succeeded from hardwoods to black spruce or balsam fir were positively associated with moderate to deep, well-drained tills. However, all 3 patterns of succession were observed on all substrates represented [139].
By analyzing archived and new data, several patterns of succession were apparent in the black spruce/feather moss and balsam fir-paper birch bioclimatic zones of central Québec. Seral sites were compared with sites that had not had fire or insect outbreaks for >100 years. Across sites, time since fire ranged from 10 to 103 years. On glaciofluvial deposits, jack pine and black spruce tended to dominate early-seral stages, with black spruce becoming increasingly dominant with time since fire (P>0.01). Successional patterns were more varied on glacial deposits. More than 30% of glacial-deposit sites in early succession were codominated or dominated by balsam fir, and balsam fir remained dominant throughout succession. About 30% were codominated or dominated by black spruce in early succession, and black spruce retained dominance throughout succession. Hardwood trees dominated early succession on about 25% of the sites; balsam fir and, to a lesser extent, black spruce, replaced the hardwoods. Jack pine dominated or codominated with black spruce on <10% of early-seral sites; black spruce eventually dominated those sites [246].
After >100 postfire years, black spruce-lichen woodlands often succeed to black spruce/moss forests on moist sites [218,219]. Such succession is unlikely on dry sites. In northern Québec, dry black spruce-lichen woodlands remained stable for 125 to 250 years. The canopy remained open, and neither feather mosses nor sphagnum mosses were replacing the lichens successionally [290].
Severe fires can slow or stop paludification. Paludification has been attributed to buildup of the moss layer, resulting in increasingly cold, humid soils and permafrost buildup [362]. Black spruce is favored successionally on cold, wet muskegs, which burn poorly in most years. A study near James Bay, Québec, found that rates of paludification in black spruce/sphagnum peatlands were faster after low-severity fires than after high-severity fires [347]. In the Clay Belt of northern Québec, conifer stands initiated after low-severity fires had low tree recruitment and slow growth relative to stands initiated after severe fires, and stands initiated after low-severity fires tended to remain open throughout succession. Jack pine tended to dominate sites that burned at high severity, while black spruce tended to dominate sites that burned at low severity (P=0.05) [247]. Low-severity fire accelerated paludification; sphagnum usually dominated the ground layer of such sites in <200 postfire years [248]. Postfire successional patterns varied with soil texture, but black spruce dominated all sites that had not burned for ≥100 years. Four burn age classes were investigated: 50 to 100 years; 100 to 150 years; 150 to 200 years; and >200 years, and 953 plots in 781 stands were measured. For sites that burned <100 years prior, black spruce dominated all sites with organic soils, while the shade-intolerant species quaking aspen and jack pine dominated 30% of sites with fine-textured soils and 60% with coarse-textured soils. Tamarack was important on late-successional sites undergoing paludification, while balsam fir was negatively associated with paludification. Overall tree species diversity was highest on burns <100 years old. Mean stand age was 154 years. Stand age was least (108 years) on coarse soils and greatest (188 years) on organics (P=0.5 for all variables) [246].The scientific name of black spruce is Picea mariana (Mill.) B.S.P. (Pinaceae) [113,121,177,210,253,344].
Natural black spruce × red spruce hybrids occur "to a limited extent" [121] in eastern Canada [121,287]. Putative black spruce × white spruce hybrids, sometimes called Rosendahl spruce, have been reported in Minnesota [121,254,395].
See Appendix B
for scientific names of plant taxa named in this review and for links to available FEIS reviews.
Black spruce is recommended for revegetating disturbed sites in boreal regions. It can be used for revegetating seismic lines, borrow pits, abandoned roads, and construction and well sites [55]. In Minnesota, Maine, and southeastern Canada, black spruce colonizes well-drained, raised surfaces in abandoned peat mines. It establishes on disturbed sites after direct seeding or transplanting [112].
Special procedures have been developed for removing black spruce seed from the semiserotinous cones [340]. Seeds retain their viability for several years when stored in sealed containers in a cool, dry environment [340]. They require no stratification prior to sowing, which is recommended soon after snowmelt [55]. On peatlands, black spruce seedling establishment is best when surface organic layers are exposed by burning or mechanical scarification. On upland sites, it is best to expose mineral soils before sowing [200].
On well-drained soils, 8- to 12-inch-tall (20-43 cm) bareroot transplants showed good growth and survival when planted directly into organic soil layers. Armson [23] recommended against removing soil organic layers when transplanting black spruce on uplands. Transplant survival and growth are generally better following summer than spring outplanting [23]. In northeastern Alberta, overwinter survival of container-grown and transplanted black spruce seedlings was "satisfactory" on amended oil sand tailings [114].
Black spruce can be propagated from root cuttings [23].
Layering occurs after mosses or litter cover black spruce's lower branches [174,396]. It is prevalent on organic soils [113] and is particularly common in swamps, bogs, and at arctic and elevational treelines. Boggy conditions in lowland black spruce/sphagnum sites promote more layering than drier conditions in upland black spruce/feather moss sites [255]. Layering may be particularly important in taiga-tundra transition zones (review by [255,256,415]). Across North America's arctic treeline, black spruce reproduces almost entirely through layering [107,113,383].
Layering may greatly increase black spruce's density in mid- to late succession, although it is not important in early postfire years [383]. In the Brooks Range of Alaska, layering was the primary method of black spruce regeneration for undisturbed stands ([256], review by [415]). Black spruce regenerated from seed in early postfire years, but later-successional regeneration was from layering [255].
Most advanced regeneration present after clearcutting is of layer origin [197,337]. Postclearcut layering is common as long as slash is not broadcast burned [314,337].
Layered branches are ladder fuels [383]. See Fuels for further information.
Root sprouting has been reported in Québec [245] and Alberta. Root sprouting may be more common than is usually realized because it is confused with layering. Excavations in Alberta found more black spruce stems originated from root sprouting (31% of total reproduction) than from branch layering (7%) [174]. Ground fires usually kill black spruce roots [264] (see Immediate Fire Effects on Plant), so root sprouting is likely only incidental in early postfire succession.
Şimali Amerika nın çimalında Labrador yarımadasından Alyaska ya kimi və cənubda Virciniya dan Vinkonsinaya qədər yayılmışdır. Hündürlüyü 20-30 m, gövdəsinin dimateri 30-90 sm, ensiz, konusvarı çətirli ağacdır: mədəni şəraitdə, əsaəsn, orta ölçülüdür. İri ağaclarda budaqları torpağa qədər sallanır. Qabığı yarıqlı, bozumtul və ya qırmızımtıl-qonur, nazikdir. Cavan zoğları qırmızımtıl-qonur, sıx, qırmızı tükcüklüdür. Tumurcuqların uzunluğu təxminən 5 mm, yumurtavarı-konusvarıdır, qatransız və ya az qatranlıdır; onların qabıqları üçbucaq, uzunsov-ucu biz, tükcüklü, qırmızı-qonurdur. İynəyarpaqları nazik, uzunluğu 6-12 (18) mm, eni 0,7-0,8 mm, dördbucaqlı, iynəli, bəzən küt, tünd göyümtül-yaşıl, çox sıx, 8-9 (14) ol qalır, sürtüldükdə ətirli olur. Qozaları yumurtavarı, xırda (uzunluğu 2-3,5 sm və eni 1,5-1,8 sm), yetişənə qədər alqırmızı-qonur, yaşlandıqda tutqun-qonur, nazik yumurtavarı qabıqlı, uzun illər (20-30 ilə qədər) ağacda qalır. Toxumların uzunluğu 2 mm, tünd-qonur, narıncı-qonur qanadı 2-3 dəfə ondan uzundur. ədəni .raitdə torpaqlara az tələbkar, kölgəyə davamlıdır. Avropa da 1700-cü ildən becərilir, az miqdarda rast gəlinir. Qışadavamlıdır, hər yerdə qozalar və toxumlar əmələ gətirir. Cənubda ilin quru dövrlərində suvarılmaya ehtiyacı var. Hətta əlverişli şəraitdə yavaş böyüyür. Kiçik ölçülərinə görə onu kiçik sahələrdə istifadə etmək olar. Küknarların digər növlərindən fərqli olaraq hər il bol meyvə verir. Ensiz çətiri və göyümtül xırda iynəyarpaqları ilə fərqlənir. Avrop ada və Şimali Amerika da qara küknarın dekorativ formalarından (“Kobold”, “Baysneri”, “Doumeti”, “Nana”, “Argenteo-varieqata”), qızılı, parlaq iynəyarpaqlı “Aurea”, sallaq çətirli “Pendula”, alçaqboylu “Empetroides”, “Erikoides” və s.-dən hələlik yaşıllaşdırmada az istifadə edilir. Azərbaycan ın cənub rayonlarında çox davamlıdır, ancaq az rast gəlinir.
Деревья и кустарники СССР. т.3.1954; Флора Азербайджана. т.5. 1954; Azərbaycanın ağac və kolları. III cild. 1970; Azərbaycanın “Qırmızı” və “Yaşıl Кitabları”na tövsiyə olunan bitki və bitki formasiyaları. 1996; Azərbaycan florasının konspekti. I-III cildlər. 2005; 2006; 2008.
Şimali Amerika nın çimalında Labrador yarımadasından Alyaska ya kimi və cənubda Virciniya dan Vinkonsinaya qədər yayılmışdır. Hündürlüyü 20-30 m, gövdəsinin dimateri 30-90 sm, ensiz, konusvarı çətirli ağacdır: mədəni şəraitdə, əsaəsn, orta ölçülüdür. İri ağaclarda budaqları torpağa qədər sallanır. Qabığı yarıqlı, bozumtul və ya qırmızımtıl-qonur, nazikdir. Cavan zoğları qırmızımtıl-qonur, sıx, qırmızı tükcüklüdür. Tumurcuqların uzunluğu təxminən 5 mm, yumurtavarı-konusvarıdır, qatransız və ya az qatranlıdır; onların qabıqları üçbucaq, uzunsov-ucu biz, tükcüklü, qırmızı-qonurdur. İynəyarpaqları nazik, uzunluğu 6-12 (18) mm, eni 0,7-0,8 mm, dördbucaqlı, iynəli, bəzən küt, tünd göyümtül-yaşıl, çox sıx, 8-9 (14) ol qalır, sürtüldükdə ətirli olur. Qozaları yumurtavarı, xırda (uzunluğu 2-3,5 sm və eni 1,5-1,8 sm), yetişənə qədər alqırmızı-qonur, yaşlandıqda tutqun-qonur, nazik yumurtavarı qabıqlı, uzun illər (20-30 ilə qədər) ağacda qalır. Toxumların uzunluğu 2 mm, tünd-qonur, narıncı-qonur qanadı 2-3 dəfə ondan uzundur. ədəni .raitdə torpaqlara az tələbkar, kölgəyə davamlıdır. Avropa da 1700-cü ildən becərilir, az miqdarda rast gəlinir. Qışadavamlıdır, hər yerdə qozalar və toxumlar əmələ gətirir. Cənubda ilin quru dövrlərində suvarılmaya ehtiyacı var. Hətta əlverişli şəraitdə yavaş böyüyür. Kiçik ölçülərinə görə onu kiçik sahələrdə istifadə etmək olar. Küknarların digər növlərindən fərqli olaraq hər il bol meyvə verir. Ensiz çətiri və göyümtül xırda iynəyarpaqları ilə fərqlənir. Avrop ada və Şimali Amerika da qara küknarın dekorativ formalarından (“Kobold”, “Baysneri”, “Doumeti”, “Nana”, “Argenteo-varieqata”), qızılı, parlaq iynəyarpaqlı “Aurea”, sallaq çətirli “Pendula”, alçaqboylu “Empetroides”, “Erikoides” və s.-dən hələlik yaşıllaşdırmada az istifadə edilir. Azərbaycan ın cənub rayonlarında çox davamlıdır, ancaq az rast gəlinir.
Picea mariana (Picea negra) és una espècie de Picea nativa del nor d'Amèrica del Nord, des de l'illa de Terranova a Alaska, i sud i nord de Nova York, Minnesota i Colúmbia Britànica central. Aquesta és una zona de bosc de taigà.[1][2][3][4][5]
Picea mariana és un arbre de creixement lent de fulla persistent. A la majoria de la seva zona de distribució arriba a fer entre 5 i 15 m d'alt però ocasionalment pot arribar als 30 m. Lews fulles són aciculars de t6-15 mm de llarg. Les pinyes són les més petites entre totes les picees, 1,5-4 cm de llarg i 1–2 cm d'ample.
Fa híbrids naturals amb Picea rubens i rarament amb Picea glauca.
Entre els seus sinònims antics estan Abies mariana, Picea brevifolia, Picea nigra.
Picea mariana és l'emblema oficial de la província canadenca de Terranova i Labrador.
La fusta és de valor menor per la seva mida petita però se'n fa paper.
Picea mariana (Picea negra) és una espècie de Picea nativa del nor d'Amèrica del Nord, des de l'illa de Terranova a Alaska, i sud i nord de Nova York, Minnesota i Colúmbia Britànica central. Aquesta és una zona de bosc de taigà.
Smrk černý (Picea mariana) je druh smrku, původem ze Severní Ameriky.
Jedná se o menší strom, zpravidla do 25 m výšky a průměru kmene do 25 cm, většinou však je spíš menší. Na extrémních stanovištích vytváří i keřovité zakrslé formy.[2] Koruna je úzce kuželovitá až jehlanovitá, tvar koruny však může být pozměněn díky stanovištním podmínkám (vítr aj.). Borka i pupeny jsou šedohnědé.[2] Jehlice jsou na průřezu čtyřhranné, poměrně krátké, jen 0,6-1,5 cm (zřídka až 2 cm dlouhé), tuhé, světle modrozelené, nasivělé, na vrcholu tupě špičaté.[2] Samičí šišky jsou celkem malé, 1,5-2,5 (zřídka až 3,5) cm dlouhé, vřetenovitého tvaru, matné, za zralosti nachově hnědé.[3] Šupiny jsou vějířovitého tvaru, na vrcholu nepravidelně zubaté, cca 8-12 mm dlouhé a asi stejně široké. Počet chromozómů je 2n=24.[2]
Původní areál druhu se rozkládá hlavně na Aljašce a v Kanadě, kde roste na většině území, chybí jen na jihozápadě a extrémním severu a severovýchodě. Přesahuje na severovýchod USA do širšího okolí Velkých jezer, do států Minnesota, Wisconsin, Michigan, Pennsylvania, New York, New Jersey, Connecticut, Rhode Island, Massachusetts, Vermont, New Hampshire a Maine.[2][3]
Smrk černý je významnou součástí severoamerické tajgy. Smrčiny s dominancí Picea mariana bývají nazývány "black spruce forests", vedle toho existují i "white spruce forests", tedy smrčiny s dominancí smrku sivého (Picea glauca). Lesy se smrkem černým najdeme především na vlhkých místech, často vytváří rašelinné lesy, kdy dominantou mechového patra jsou rašeliníky (Sphagnum sp.).[4] Společenstva se smrkem černým se nachází i na jiných podmáčených místech, jako břehy potoků a okraje močálů.[5] Vytváří lesy i mimo rašeliniště, s dobře vyvinutým mechovým patrem, častý např. Pleurozium schreberi. Tam, kde jsou rašeliníky řídké nebo chybí, je v keřovém patře častý druh rojovníku Ledum groenlandicum.[4] Hojné jsou taky zakrslé řídkolesy na bažinách, kde v bylinném patře dominují ostřice (Carex sp.) a trávy, dobře je vyvinuto mechové patro (ovšem jen málo rašeliníky).[4] Dále jsou známy smíšené lesy s olší šedou (Alnus incana).[4] Dalšími dřevinami v lesích se smrkem černým jsou např. jedle balzámová (Abies balsamea), topol osikovitý (Populus tremuloides), bříza papírovitá (Betula papyrifera), smrk sivý (Picea glauca) nebo modřín americký (Larix laricina).[4] Smrk černý snáší i velmi kyselé a živinami chudé půdy. Je často napadán poloparazitickou rostlinou Arceuthobium pusillum, příbuznou se jmelím.[6] Při větším napadení může docházet k oslabení stromu, deformaci až úhynu.[4] Porosty smrku černého mohou být disturbovány větrem nebo požáry. Uschnutí porostu může způsobit i trvalejší zaplavení, např. díky bobřím hrázím. Smrk černý je také napadán kůrovcem Dendroctonus rufipennis, i když jen příležitostně. Daleko více je napadán smrk sivý, kdy jsou známy rozsáhlé kůrovcové kalamity na Aljašce a v Kanadě o rozloze v řádu tisíců km².[7] Kromě kůrovce je smrk černý napadán i jiným hmyzem, jako housenkami můr z rodu Choristoneura, larvami brouků rodu Monochamus, larvami hmyzu z řádu blanokřídlí Pikonema alaskensis[8] a Pikonema dimmockii[4] a dalším hmyzem. Jsou známy i různé houbové choroby.
Smrčina s dominancí smrku černého
Kalamitou postižená smrčina
Smíšený les smrku černého a modřínu amerického
Porost smrku černého
Z volné přírody, na narušovaných stanovištích východní Kanady, je znám kříženec s druhem Picea rubens.[2]
Využití v lesnictví je oproti jiným druhům smrků omezené díky menšímu vzůstu. Dřevo lze využít k výrobě papíru aj.[2] Smrk černý se pěstuje i ve střední Evropě jako okrasný strom ve více kultivarech. V Čechách byl poprvé vysazen roku 1835 v Královské oboře. Rozšířené je spíš pěstování různých zakrslých kultivarů.[9]
Obrázky, zvuky či videa k tématu smrk černý ve Wikimedia Commons
Galerie smrk černý ve Wikimedia CommonsSmrk černý (Picea mariana) je druh smrku, původem ze Severní Ameriky.
Sortgran (Picea mariana) er et mellemstort, stedsegrønt nåletræ med en tætgrenet, kegleformet vækst og en meget smal top. Hovedgrenene er korte og hængende med opadbøjede spidser.
Barken er først rødbrun og behåret. Senere bliver den rødgrå og afskallende, og på gamle grene og stammer er den rødligt mørkegrå med små, grå skæl. Knopperne er omvendt ægformede og lysebrune. Nålene er tynde, stive og firkantede i tværsnit, og de sidder tæt hele vejen rundt om skuddet. Oversiden er mørkegrøn med et blåligt skær, mens undersiden har to lyseblå striber.
De hanlige blomster findes i små, højrøde og kegleformede stande, der sidder tæt overalt på planten. De hunlige blomster er samlet i små røde, oprette stande, der sidder i toppen af træet. Koglerne er ægformede og i begyndelsen rødlige, men senere bliver de rødbrune og skinnende. Frøene er vingede.
Rodnettet er normalt fladt og højtliggende, men på gode voksesteder kan der udvikles en pælerod. Arten har mykorrhiza med hulstokket rørhat (Suillus cavipes), rød ametysthat (Laccaria laccata), tvefarvet ametysthat (Laccaria bicolor), Pisolithus tinctorius og med arter af slægterne Cenococcum og skægtrøffel (Rhizopogon).
Højde x bredde og årlig tilvækst: 15 x 2 m (10 x 3 cm/år), men størrelsen aftager, hvor forholdene er mere barske. Ved skovgrænsen opnår træet præcis den højde, som er bestemt af snelagets tykkelse.
Sortgran er udbredt i hele det trædækkede Canada og Alaska, hvor den danner skovgrænse ind mod tundraen. Desuden findes arten spredt på sure og våde biotoper i USA's stater ved de store søer og i New England.
I provinsen Manitobas lavland op mod Hudsonbugten, Canada, finder man en åben skovtype, hvor arten er dominerende over en vegetation med bl.a. arktisk pil, blåbærpil, fjeldrevling, hvidgran, sumpbirk og tyttebær[1]
Sortgran (Picea mariana) er et mellemstort, stedsegrønt nåletræ med en tætgrenet, kegleformet vækst og en meget smal top. Hovedgrenene er korte og hængende med opadbøjede spidser.
Die Schwarz-Fichte (Picea mariana) ist eine immergrüne Baumart aus der Gattung der Fichten (Picea) innerhalb der Familie der Kieferngewächse (Pinaceae), die im nördlichen Nordamerika heimisch ist.
Die Schwarz-Fichte wächst je nach Standortbedingungen als immergrüner Baum oder Strauch. Die Baumform erreicht Wuchshöhen von 6 bis 35 Meter und Brusthöhendurchmesser von etwa 25 Zentimeter. Die vollholzigen Stämme sind kerzengerade. Jungbäume besitzen eine schmale und regelmäßig aufgebaute Krone, die schmal-kegelförmige Krone der Altbäume ist eher offen und unregelmäßig aufgebaut. Die relativ kurzen und dünnen Äste sitzen waagerecht an den Stämmen. Sie sind herabhängend und richten sich an der Spitze wieder auf. Die Strauchform findet man vor allem an der Waldgrenze. Die Schwarz-Fichte wächst sehr langsam, meist nur 15 bis 25 Zentimeter pro Jahr.
Die eiförmigen Knospen sind hell rötlich-braun, werden etwa 5 Millimeter lang und sind harzfrei. Die dicht stehenden Nadeln sind 6 bis 18 Millimeter lang und etwa 0,8 Millimeter breit. Sie sind im Querschnitt viereckig geformt. Die Nadeloberseite ist mattgrün bis blaugrün. An der Oberseite sitzen ein bis zwei und an der Nadelunterseite drei bis vier weißliche Spaltöffnungsreihen. Der Apex ist kurz zugespitzt. Die Nadeln sind ab der Mitte oft ein wenig einwärts gekrümmt. Sie stehen an der Zweigoberseite radiär und an der Unterseite mehr oder weniger gescheitelt angeordnet. Die zerriebenen Nadeln duften aromatisch. Sie verbleiben zwischen 5 und 13 Jahren am Baum, ehe sie abfallen.
Die Schwarz-Fichte ist einhäusig-getrenntgeschlechtig (monözisch) und ist zur Selbstbefruchtung fähig. Sie wird mit 7 bis 10 Jahren mannbar, wobei bis zu einem Alter von 14 Jahren hauptsächlich weibliche Blütenzapfen gebildet werden. Später verhält es sich umgekehrt. Die Blütezeit erstreckt sich von Ende Mai bis Anfang Juni. Die aufrecht stehenden und grün bis purpurrot gefärbten weiblichen Blütenzapfen werden ausschließlich an der Kronenspitze gebildet. Die dunkelroten männlichen Blütenzapfen werden 12 bis 20 Millimeter lang und werden an der Peripherie der Krone gebildet. Es können im Grenzbereich der Zonen von männlichen und weiblichen Blütenzapfen zweigeschlechtige Blütenstände entstehen. Die anfangs dunkelvioletten später braunen Zapfen reifen etwa drei Monate nach der Blüte. Sie werden zwischen 1,5 und 3,8 Zentimeter lang und zwischen 1,5 und 1,8 Zentimeter dick. Die Zapfen bestehen aus rundlichen bis eiförmigen Zapfenschuppen. Diese sind steif, spröde und am Rand fein gesägt. Die Zapfen sitzen an einen rund 2 Millimeter langen gekrümmten Stiel. Die Samen werden hauptsächlich im Frühjahr entlassen. Manche Zapfen öffnen sich erst bei Hitzeeinwirkung, wie sie zum Beispiel bei Waldbränden auftritt, um die Samen freizulassen. Die leichten, schokoladebraunen Samen sind geflügelt und sind ohne Flügel rund 2,5 Millimeter lang. Mit Flügel sind sie rund 10 Millimeter lang. Der spitz auslaufende Samenflügel ist oberhalb der Mitte am breitesten. Die Samen werden selten mehr als 80 Meter vom Baum fortgetragen. Das Tausendkorngewicht liegt zwischen 1,3 und 1,5 Gramm. Die Sämlinge besitzen 2 bis 7 Keimblätter (Kotyledonen). Die Chromosomenzahl beträgt 2n = 24.
Die Entwicklung des Wurzelsystems wird von der Bodenbeschaffenheit bestimmt. Während die Baumform tiefwurzelnd ist, wurzelt die Strauchform flach. Anhand der Untersuchung eines 130-jährigen Bestandes in Alaska nimmt man an, dass das Wurzelsystem rund 15 % der gesamten Biomasse ausmacht. Die Art geht Mykorrhiza-Partnerschaften mit dem Hohlfußröhrling (Suillus cavipes), mit dem Rötlichen Lacktrichterling (Laccaria laccata), mit Laccaria bicolor, mit Pisolithus tinctorius sowie mit Arten der Gattungen Cenococcum und Rhizpogon ein.
Die Rinde der jungen Triebe ist rostbraun und dicht drüsig behaart, verkahlt aber nach und nach. Bei älteren Trieben ist die Rinde dunkel. Sie bilden im zweiten Jahr erste dünne Borkenschuppen aus. Die Schuppenborke der Altbäume ist schwärzlich-graubraun gefärbt und wird selten dicker als 1,2 Zentimeter. Die innere Rinde soll je nach Quelle olivgrün bis gelbgrün gefärbt sein.
Das Kernholz ist gelblich-weiß gefärbt und wird von einem sehr schmalen und etwas helleren Splint umgeben. Das Holz ist relativ weich. Harzkanäle finden sich vor allem im Spätholz. Die Rohdichte beträgt rund 0,48 g/cm³. Sie ist im Norden des Verbreitungsgebietes höher als im Süden. Die Jahresringe sind deutlich zu erkennen.
Die Schwarz-Fichte ist in ganz Kanada und der nördlichen USA heimisch. Sie ist die häufigste Baumart im Borealen Schild. Ihr Areal reicht von der Ostküste Labradors bis zur Westküste Alaskas. Die Südgrenze des geschlossenen Verbreitungsgebietes befindet sich im Gebiet der Großen Seen, es gibt aber auch Einzelvorkommen in New Jersey, Virginia und Pennsylvania. Man findet sie nordwärts bis zur polaren Waldgrenze. Sie wird in Europa nur selten angepflanzt.
Die Schwarz-Fichte ist eine Pionierart auf Brand- und Sturmflächen. Sie ist an extreme Klima- und Standortbedingungen angepasst und wächst auch auf Permafrostböden. Es werden selbst arme, vernässte, anmoorige, schwach staunasse, vergraste und spätfrostgefährdete Standorte besiedelt. Optimale Standorte bieten kalkführende Mineralböden, Lehm- und Tonböden, sowie Moränen und Flusstrassen. Der pH-Wert sollt neutral bis schwach alkalisch sein. An ihren natürlichen Standorten können die Temperaturmaxima bzw. -minima −62 °C und +41 °C erreichen. Die Jahresniederschläge liegen zwischen 150 und 1.520 mm, wovon ein Großteil als Schnee fällt. Sie kommt vom Tiefland bis in Höhenlagen von 1.800 Metern vor. Im südlichen Teil des Verbreitungsgebietes bildet die Art Mischwälder mit Banks Kiefer (Pinus banksiana), der Weymouths-Kiefer (Pinus strobus), der Rot-Erle (Alnus rubra), der Schwarz-Esche (Fraxinus nigra) und dem Abendländischen Lebensbaum (Thuja occidentalis).
Die Schwarz-Fichte ist einer der wichtigsten Holzlieferanten für die Papier- und Zellstofferzeugung in Kanada. Sägeware fällt aufgrund der geringen Dimensionen kaum an. Früher fand das Holz Verwendung als Grubenholz. Die Indianer gewannen aus den Wurzeln ein Bindematerial, das sie zum Herstellen ihrer Kanus benutzten. Die Art wird auch als Christbaum genutzt. Sie findet nur selten Verwendung als Ziergehölz.
Für die Schwarz-Fichte stellen Waldbrände und Windwurf eine größere Gefahr dar als biotische Schädlinge. Sie reagiert empfindlich auf Fluorwasserstoff. Die Raupen des Wicklers Choristoneura fumiferana fressen die Nadeln und können bei starken Befall zum Tod der Pflanze führen. Als Holzschädling wird der Borkenkäfer Dendroctonus rufipennis genannt, der besonders häufig in Mischkulturen mit der Weiß-Fichte (Picea glauca) auftritt. An Schadpilzen werden der Gemeine Hallimasch (Armillaria mellea), Chrysomyxa ledicola, Chrysomyxa pirolata und Gremmeniella abietina genannt. Schneeschuhhasen (Lepus americanus) verbeißen die Zweige bis zu einer Höhe von 2 Metern.
Die Schwarz-Fichte wird von Schmidt innerhalb der Fichten (Picea) in die Untergattung Picea und die Sektion Picea gestellt. Willkomm ordnete die Art innerhalb der Fichten der Sektion Eupicea zu. Die Schwarz-Fichte bildet natürliche Hybride mit der Weiß-Fichte (Picea glauca) und der Amerikanischen Rot-Fichte (Picea rubens). Es werden auch künstliche Hybride mit der Serbischen Fichte (Picea omorika), der Gemeinen Fichte (Picea abies), der Ajan-Fichte (Picea jezoensis) und mit der Sitka-Fichte (Picea sitchensis) gezüchtet.
Synonyme für Picea mariana (Mill.) Britton, Sterns & Poggenb. sind: Abies mariana Mill., Picea brevifolia Peck, Picea mariana var. brevifolia (Peck) Rehder, Picea nigra (Castigl.) Link, Pinus nigra Aiton nom. illeg., Pinus mariana (Mill.) Münchh., Pinus canadensis var. nigricans Weston.[1]
Die Schwarz-Fichte (Picea mariana) ist eine immergrüne Baumart aus der Gattung der Fichten (Picea) innerhalb der Familie der Kieferngewächse (Pinaceae), die im nördlichen Nordamerika heimisch ist.
Must kuz' (latin.: Picea mariana) om kuzen levitadud erik.
Kazvab kavag'mecoiš Kanadadme, AÜV:oiden Aläskas i pohjoižpäivnouzmaižiš štatoiš.
Сьӧд кыз (лат. Picea mariana) – Pinaceae семьяысь Уйпал Америкаын будӥсь кыз. Ӝуждалаез ог 15-50 м, модослэн диаметрез 30-60 см.
Picea mariana, the black spruce, is a North American species of spruce tree in the pine family. It is widespread across Canada, found in all 10 provinces and all 3 territories. It is the official tree of the province of Newfoundland and Labrador and is that province's most numerous tree. The range of the black spruce extends into northern parts of the United States: in Alaska, the Great Lakes region, and the upper Northeast. It is a frequent part of the biome known as taiga or boreal forest.[3][4][5][6][7]
The Latin specific epithet mariana means “of the Virgin Mary”.[8]
P. mariana is a slow-growing, small upright evergreen coniferous tree (rarely a shrub), having a straight trunk with little taper, a scruffy habit, and a narrow, pointed crown of short, compact, drooping branches with upturned tips. Through much of its range it averages 5–15 m (15–50 ft) tall with a trunk 15–50 cm (6–20 in) diameter at maturity, though occasional specimens can reach 30 m (98 ft) tall and 60 cm (24 in) diameter. The bark is thin, scaly, and grayish brown. The leaves are needle-like, 6–15 mm (1⁄4–9⁄16 in) long, stiff, four-sided, dark bluish green on the upper sides, paler glaucous green below. The cones are the smallest of all of the spruces, 1.5–4 cm (1⁄2–1+1⁄2 in) long and 1–2 cm (1⁄2–3⁄4 in) broad, spindle-shaped to nearly round, dark purple ripening red-brown, produced in dense clusters in the upper crown, opening at maturity but persisting for several years.[3][4]
Natural hybridization occurs regularly with the closely related P. rubens (red spruce), and very rarely with P. glauca (white spruce).[3]
It differs from P. glauca in having a dense cover of small hairs on the bark of young branch tips, an often darker reddish-brown bark, shorter needles, smaller and rounder cones, and a preference for wetter lowland areas. Numerous differences in details of its needle and pollen morphology also exist but require careful microscopic examination to detect. From true firs, such as Abies balsamea (balsam fir), it differs in having pendulous cones, persistent woody leaf-bases, and four-angled needles, arranged all round the shoots.
Due to the large difference between heartwood and sapwood moisture content, it is easy to distinguish these two wood characteristics in ultrasound images,[9] which are widely used as a nondestructive technique to assess the internal condition of the tree and avoid useless log breakdown.
Older taxonomic synonyms include A. mariana, P. brevifolia, or P. nigra.
Growth varies with site quality. In swamp and muskeg it shows progressively slower growth rates from the edges toward the centre. The roots are shallow and wide spreading, resulting in susceptibility to windthrow. In the northern part of its range, ice pruned asymmetric black spruce are often seen with diminished foliage on the windward side.[10] Tilted trees colloquially called "drunken trees" are associated with thawing of permafrost.[3][11]
In the southern portion of its range it is found primarily on wet organic soils, but farther north its abundance on uplands increases. In the Great Lakes region it is most abundant in peat bogs and swamps, also on transitional sites between peatlands and uplands. In these areas it is rare on uplands, except in isolated areas of northern Minnesota and the Upper Peninsula of Michigan.
Most stands are even-aged due to frequent fire intervals in black spruce forests. It commonly grows in pure stands on organic soils and in mixed stands on mineral soils. It is tolerant of nutrient-poor soils, and is commonly found on poorly drained acidic peatlands. It is considered a climax species over most of its range; however, some ecologists question whether black spruce forests truly attain climax because fires usually occur at 50 to 150 year intervals, while "stable" conditions may not be attained for several hundred years.[3]
The frequent fire return interval, a natural fire ecology, perpetuates numerous successional communities. Throughout boreal North America, Betula papyrifera (paper birch) and Populus tremuloides (quaking aspen) are successional hardwoods that frequently invade burns in black spruce. Black spruce typically seeds in promptly after fire, and with the continued absence of fire, eventually dominates the hardwoods.
Black spruce is a pioneer that invades the sphagnum mat in filled-lake bogs, though often preceded slightly by Larix laricina (tamarack). Black spruce frequently out-competes shade-intolerant tamarack in the course of bog succession.[12] However, as the peat soil is gradually elevated by the accumulation of organic matter, and the fertility of the site improves, balsam fir and northern white cedar (Thuja occidentalis) eventually replace black spruce and tamarack. On drier sites following fires, black spruce can take over stands of faster growing jack pine (Pinus banksiana) by virtue of its ability to grow in partially shaded conditions which inhibit pine seedlings.[13] But black spruce seedlings are themselves intolerant to the low light and low moisture conditions under mature spruce stands. Balsam fir and northern white cedar, both more understory-tolerant species with deeper taproots, survive and eventually succeed the spruce in the absence of fire.[14]
The spruce budworm, a moth larva, causes defoliation, which kills trees if it occurs several years in a row, though black spruce is less susceptible than white spruce or balsam fir. Trees most at risk are those growing with balsam fir and white spruce.[15]
Numerous cultivars have been selected for use in parks and gardens. The cultivar P. mariana 'Nana' is a dwarf form which has gained the Royal Horticultural Society's Award of Garden Merit.[16][17]
Balsam fir is known to hybridize with Serbian spruce, Picea omorika. The hybrid is Picea machala, and hybrids with Sitka spruce are known as well.
Black spruce is the provincial tree of Newfoundland and Labrador.
The timber is of low value due to the small size of the trees, but it is an important source of pulpwood and the primary source of it in Canada.[18] Fast-food chopsticks are often made from black spruce.[5]
However, it is increasingly being used for making cross laminated timber by companies such as Nordic Structures, which allows the high strength due to the tight growth rings to be assembled into larger timbers.[19]
Along with red spruce, it has also been used to make spruce gum and beer.[20]
Boggy taiga habitat
Lit by the midnight sun in Ivvavik National Park
Immature cones
Mature, open cones
Seeds
Media related to Picea mariana at Wikimedia Commons
Picea mariana, the black spruce, is a North American species of spruce tree in the pine family. It is widespread across Canada, found in all 10 provinces and all 3 territories. It is the official tree of the province of Newfoundland and Labrador and is that province's most numerous tree. The range of the black spruce extends into northern parts of the United States: in Alaska, the Great Lakes region, and the upper Northeast. It is a frequent part of the biome known as taiga or boreal forest.
The Latin specific epithet mariana means “of the Virgin Mary”.
Picea mariana, la pícea negra, es una especie arbórea perteneciente a la familia de las pináceas, género de las píceas.
Es originaria de Norteamérica, desde la Isla de Terranova hasta el oeste de Alaska, y más al sur llegan hasta el norte de New York, Minnesota y hasta la zona central de la Columbia Británica.
Esta área es también conocido como el “bioma forestal” denominado Taiga.[1][2][3][4][5]
Se trata de una especie de Pinophyta o conífera de crecimiento lento, de posición vertical. Es un árbol pequeño, siempre verde, (rara vez como arbusto), con un tronco recto, copa de aspecto desaliñada, estrecha con ramas colgantes más bien cortas, compactas, y con las puntas hacia arriba.
Generalmente su rango promedio es de 5.15 m de altura con un tronco de 15-50 cm de diámetro en su madurez, aunque pueden hallarse ejemplares que llegan a alcanzar los 30 m de altura y 60 cm de diámetro. Su corteza es delgada, escamosa, y de color marrón grisáceo. Las hojas son como agujas, de 6-15 mm de largo, rígidas, de cuatro lados, de color verde azulado oscuro en los lados superiores , verde pálido en la parte inferior. Las piñas en forma de cono (coníferas) son las más pequeñas de todos los abetos, entre 1.5 y 4 cm de largo y de 1 a 2 cm de ancho, con forma de hueso de color rojo o púrpura oscuro, y de color marrón cuando están maduras, formando densos racimos en la corona superior. La piña se abre cuando está madura y persiste en el árbol durante varios años.[1][2]
Suelen presentarse regularmente casos de hibridación natural entre las píceas negras y su pariente cercano la pícea roja (Picea rubens), y raramente se cruza con la pícea blanca (Picea glauca).[1]
La pícea negra se diferencia de la pícea blanca en que las agujas son más cortas, las piñas más pequeñas y redondas, y tiene mayor preferencia por las zonas de tierras húmedas bajas. A diferencia de las especies primarias como el Abies balsamea (abeto balsámico), difiere en que tienen piñas colgantes, hojas persistente a modo de agujas de 4 lados desde la base del brote.
El crecimiento varía según las condiciones del lugar. En pantanos muestra tasas de crecimiento más lento, desde los bordes hacia el centro. Las raíces son poco profundas y de gran difusión entre árboles caídos, coloquialmente llamados "árboles borrachos", y se asocian a menudo con el descongelamiento del permafrost.[1][4][5]
En las zonas más septentrionales, la pícea negra sufre a menudo una asimétrica poda de hielo, donde disminuye su follaje del lado de barlovento.[6]
Crece tanto en tierras bajas como en montañas. En la parte sur de su distribución se encuentra principalmente en suelos orgánicos húmedos, pero más al norte, abunda sobre las pendientes de las montañas. En los grandes lagos es más abundante en las turberas y pantanos, también en los sitios de transición entre las tierras altas y las turberas. En estas áreas es raro verlos sobre las montañas, excepto en zonas aisladas del norte de Minnesota y la Península Superior de Míchigan.
En los bosques de píceas negras, la mayoría de los ejemplares tienen la misma edad, debido a los intervalos de los incendios frecuentes. Comúnmente crecen formando bosques puros sobre suelos orgánicos y en bosques mixtos en los suelos más minerales. Es tolerante a suelos pobres en nutrientes, y se encuentra comúnmente en las turberas de mal drenaje ácido. Se considera una especie de punto culminante en la mayor parte de su gama. Sin embargo, algunos ecologistas se preguntan si los bosques de píceas negras realmente alcanzan el clímax alguna vez; porque los incendios ocurren generalmente a intervalos de 50-150 años, mientras que en condiciones "estables" un ejemplar puede alcanzar varios cientos de años de edad.[1]
La frecuencia de retorno a intervalos regulares de los incendios, perpetúa numerosas comunidades sucesivas. A lo largo de América del Norte boreal los abedules como el Abedul de los cánoes, o el Populus tremuloides, que son de madera más duras, con frecuencia invaden las zonas quemadas de los bosques de píceas negras. La Pícea negra se regenera por medio de semillas, inmediatamente después del fuego, y con la continua ausencia de fuego, finalmente terminan dominando las especies de madera dura.
Es un pionero que invade la alfombra llena de juncos en los lagos y pantanos, aunque a menudo es precedido por el Alerce oriental (Larix laricina), con el que forma con el tiempo de una cubierta forestal estable en los pantanos. Sin embargo, en la turba es poco elevado por la acumulación de materia orgánica y la fertilidad que el lugar ofrece, favoreciendo al Abeto balsámico (Abies balsamea) y la Tuya occidental (Thuja occidentalis) que termina finalmente reemplazando a la Pícea negra y a los alerces.
Las larvas de la polilla Larva Spruce causan defoliación y si ocurre durante muchos años en el tronco, produce la muerte, aunque la pícea negra es menos susceptible que el abeto blanco o el balsámico. Los árboles de mayor riesgo son los que crecen con el abeto balsámico y el abeto blanco.
La Pícea negra es el “Árbol emblemático Provincial de Canadá” de Terranova y Labrador.
Su madera es de un valor bajo debido al pequeño tamaño de los troncos, pero se utiliza para pulpa y papel.
Picea mariana fue descrita por (Mill.) Britton, Sterns & Poggenb. y publicado en Preliminary Catalogue of Anthophyta and Pteridophyta Reported as Growing Spontaneously within One Hundred Miles of New York 71. 1888.[7]
Picea; nombre genérico que es tomado directamente del Latín pix = "brea", nombre clásico dado a un pino que producía esta sustancia[8]
mariana: epíteto
Picea mariana, la pícea negra, es una especie arbórea perteneciente a la familia de las pináceas, género de las píceas.
Must kuusk (Picea mariana) on igihaljas okaspuuliik kuuse perekonnast. Nad kasvavad Alaskal, Kanadas ja USA kirdeosas, niiske või mõõdukalt niiske kliimaga aladel meretasemel ja mägedes kuni 1830 m kõrgusel. Puude eluiga on 200–300 aastat ja need kasvad 10–15 m, harva kuni 30 m kõrguseks.
Puu kasvab looduslikus levilas keskmiselt 10–15, harva kuni 30 m kõrguseks. Tüve läbimõõt on tavaliselt kuni 30, harva kuni 90 cm.[3] Levila põhjaosa karmides ilmastikutingimustes on 100–200 aasta vanused puud sageli 3–6 m kõrgused ning tüve läbimõõt on 2,5–5,0 cm.[4]
Eluiga ei küündi tavaliselt üle 200 aasta, harva kuni 300 aastani.[5]
Tüve koor on hallikas- või punakaspruun, vanemas eas mustjas ja tugevalt kestendav.[3]
Juurestik on maapinnalähedane, ulatudes keskmiselt 18–30, maksimaalselt 60 cm sügavusele. Peenema tüve ja maapinnalähedase juurestiku tõttu esineb sageli tormimurdu ja -heidet.[5]
Võra on üsna kitsas, koonusjas-kuhikja, sageli ebasümmeetrilise kujuga, valgusküllases kasvukohas ulatub maapinnani. Oksad asetsevad noores eas horisontaalselt, vanemas eas rippuvad.[3]
Võrsed on punakaspruunid, tihedalt hatukarvased.[3] Pungad on punakaspruunid, vaiguta, pikkade pungasoomustega, karvakestega kaetud.[6]
Okkad on tömbid või lühidalt teritunud, 0,6–1,2 (1,8) cm pikkused, sinakasrohelised kuni tumerohelised, asetsevad väga tihedalt, sirged või nõrgalt kõverdunud, pealpool 3–4, allpool 1–2 õhulõherida.[3]
Käbid on 2–3,5 cm pikkused ja läbimõõduga 1,2–1,8 cm, munajad kuni ümardunud, pika rootsuga, õitsemisel punased, valminult tumevioletjaspruunid, on sageli tihedas kobaras, peale seemnete varisemist jäävad mõneks aastaks puule. Seemnesoomuse väljaulatuv osa on kolmnurkjas kuni ümar, serv tipuosas paksenenud, ebaühtlaselt peensaagjas, laineline.[3]
Seemned on 2–3 (4) mm pikkused, tumepruunid, läikivad, 6–9 (15) mm pikkuse tiivakesega.[6] Põhja-Ameerika kuuskede seas on musta kuuse seemned kõige väiksemad, 1000 seemne mass on keskmiselt 1,1 g.[4]
Musta kuuse levikuala laiub suurel territooriumil Põhja-Ameerikas – Alaskal, Kanadas ja USA kirdeosas. Kasvab merepinna kõrgusel Kanada ida- ja põhjaosas ning Alaska lääneosas. Mägedes tõuseb kuni 1830 m kõrgusele (Alberta provintsi põhjaosas).[5]
Levikuala kliimat iseloomustavad väga külmad talved ja niiske kuni mõõdukalt niiske õhk. Aasta keskmine õhutemperatuur on vahemikus +7 °C levila lõunaosas kuni –11 °C Kanada kesk- ja lääneosas. Jaanuari keskmine õhutemperatuur on –30 °C Kanada loodeosas ja Alaskal ning –6 °C levila kaguosas. Juuli keskmine õhutemperatuur jääb vahemikku +10...+26 °C. Levikuala minimaalsed temperatuurid jäävad vahemikku –34...–62 °C, maksimaalsed +27...+41 °C. Sademete hulk väheneb läänest itta. Maksimaalselt sajab Atlandi ookeani rannikupiirkonnas – 1520 mm, minimaalselt Alaska lääneosas – 150 mm. Suuremal osal levikualast jääb keskmine sademete hulk siiski vahemikku 380...760 mm.[5]
Must kuusk kasvab peamiselt märgadel ja happelistel turvasmuldadel. Kasvupinnastest esinevad veel huumusrikkad mullad, soostunud pinnased, moreen, liivmuld ja õhukesed mullad kaljude nõlvadel. Moodustab puhtpuistuid eelkõige turbamuldadel ja segametsi mineraalmuldadel. Must kuusk on tavaliselt madal ja aeglase kasvuga. Levinud eelkõige tasandikel ja madalikel, kuid teda leidub ka mägedes.[5] Levila põhjaosas on must kuusk sageli enamuspuuliik igikeltsa aladel.[4]
Musta kuuse metsad on regulaarselt puhkevate metsapõlengute tõttu ühevanused. Ta moodustab puhtpuistuid ja segametsi peamiselt koos järgmiste puuliikidega: kanada kuusk (Picea glauca), palsamnulg (Abies balsamea), hall mänd (Pinus banksiana), ameerika lehis (Larix laricina), paberikask (Betula papyrifera), keerdmänd (Pinus contorta), ameerika haab (Populus tremuloides), punane kuusk (Picea rubens), palsampappel (Populus balsamifera), harilik elupuu (Thuja occidentalis), must saar (Fraxinus nigra), ameerika jalakas (Ulmus americana), punane vaher (Acer rubrum) jt.[5]
Musta kuuse looduslikud hübriidid:
Kuusepüüd (Falcipennis canadensis) toituvad talvel (Alaskal novembrist märtsini) ainult kuuseokastest ning elutsevad peamiselt kuusikutes. Samuti on musta kuuse pungad, kambium ja võrsed oluliseks toidulisaks ameerika jänesele (Lepus americanus). Ameerika punaoravad söövad koguvad musta kuuse käbisid, et sealt hiljem seemneid süüa. Siiski maitsevad neile rohkem kanada kuuse seemned. Nad toituvad sügisel ja talvel peamiselt seemnetest, kevadel puu võrsetest ja pungadest. Mahalangenud seemneid koguvad hiired ja vöötoravad. Seemnetest toituvad ka mitmed linnuliigid, näiteks ameerika põhjatihane (Poecile atricapillus), mägitihane (P. gambeli), kanada tihane (P. hudsonicus), ruskselg-tihane (P. rufescens), valgekulm-puukoristaja (Sitta canadensis), kuuse-käbilind (Loxia curvirostra), vööt-käbilind (L. leucoptera) ja männisiisike (Carduelis pinus). Rubiin-pöialpoiss (Regulus calendula), tsuugasäälik (Dendroica magnolia), kuusesäälik (D. tigrina) ja maasäälik (Seiurus aurocapillus) pesitsevad peamiselt musta kuuse metsades.[4]
Must kuusk on ühekojaline ning paljuneb peamiselt seemnetega. Samas suudab ka vegetatiivselt paljuneda alumiste okste juurdumisega. Seda eriti piirkondades, kus kiirelt kasvav sammal katab aeglaselt kasvavad seemikud. Käbikandvus algab väga soodsatel tingimustel juba 10 aasta vanuselt, kuid esineb siis üksikute käbidena. Tavaliselt algab käbikandvus siiski 30 aasta vanustel puudel ja kestab kuni 250 aasta vanuseni. Parimat saaki annavad puud vanuses 100–200 aastat.[5]
Puu tolmleb mai lõpust juuni alguseni. Levikuala põhjapoolsemad puud tolmlevad 1–2 nädalat lõunapoolsematest hiljem. Emasõisikud on õitsemise ajal 15–25 mm pikkused, rohelised või purpursed, asetsevad ladva viimasel meetril, eelmise aasta võrsete tipul ja on üldjuhul püstised. Isasõisikud on õitsemise ajal tumepunased või purpurjad, munajad, 12–20 mm pikkused, paiknevad allpool emasõisikuid, kollaste tolmukatega, peale õitsemist pruunikad. Seemned valmivad kolm kuud peale tolmlemist, augusti lõpust kuni septembri alguseni. Head seemneaastad korduvad 2–6 aasta järel, harvemini esineb neid levikuala põhjapoolsemates, karmi kliimaga piirkondades. Käbid ei avane karmi kliimaga piirkondades täielikult ning seemnete varisemine võib kesta mitu aastat. Reeglina langevad seemned puust mitte kaugemale kui 80 m. Enamus seemneid variseb talvel ja kevadel. Seemnete idanevus on ligi 88%.[4][5]
Noored puud taluvad reeglina hästi varju, kuid kõige paremini kasvavad siiski täisvalguses. Esimese kasvuperioodi lõpuks on puud harva kõrgemad kui 2,5 cm ning nende juurestik võib ulatuda kuni 5 cm sügavusele. Kolmeaastased seemikud on tavaliselt 7–13 cm kõrgused.[4]
Musta kuuse puit on helekollase tooniga, kerge, keskmise elastsuse ning tugevusomadustega. Kanadas on musta kuuse puit kõige olulisem tooraine kõrge kvaliteediga tselluloosi valmistamisel. Puitu kasutatakse veel ehitusmaterjalina ja kasvatatakse jõulupuuna (eriti Minnesotas).[5] Okastest saab valmistada eeterlikku õli ning musta kuuse kultivare kasvatatakse vähesel määral ka ilupuudena. Puidu füüsikalised ja mehaanilised omadused on toodud alljärgnevas tabelis:[7][8]
Omadus Väärtus Ühik Tihedus, õhukuiv puit* 470 kg/m3 Erikaal, õhukuiv puit* 0,42 Elastsusmoodul, värske puit / õhukuiv puit* 9500 / 11100 MPa Paindetugevus, värske puit / õhukuiv puit* 42,0 / 74,0 MPa Survetugevus, (õhukuiv puit*) pikikiudu / ristikiudu 41,1 / 3,8 MPa Nihketugevus, värske puit / õhukuiv puit* 5,1 / 8,5 MPa Ruumala kahanemine kuivamisel, ahjukuiv puit** 11,3 % * – niiskusesisaldus 12%; ** – niiskusesisaldus 0%.Must kuusk toodi Euroopasse esmakordselt juba aastal 1700, Eestisse jõudis 19. sajandil. Meie kliima sobib talle üsna hästi. Ta on meil täiesti külmakindel, kannab rikkalikult käbisid ning seemnete kvaliteet on väga hea (idanevus kuni 80%). Mulla kuivust ei talu, kuid kasvab soostunud aladel, eelistab niisket õhku. Aeglasekasvulisena ta meie metskultuuri ei sobi, kuid väärib kasvatamist parkides ja haljasaladel oma ilusa sihvaka võra ja sinakasrohelise okastiku tõttu. Meil on musta kuuske rohkem hakatud kasvatama möödunud sajandil. Viljakandvaid puid võib leida Järvseljal, Luual, Tihemetsa dendraariumis, Tartus jm. Samuti on Soomes (Mustilas, Punkaharjus, Ruotsinkyläs jm) musta kuuse metsastamisel saadud häid tulemusi.[3][6]
Must kuusk (Picea mariana) on igihaljas okaspuuliik kuuse perekonnast. Nad kasvavad Alaskal, Kanadas ja USA kirdeosas, niiske või mõõdukalt niiske kliimaga aladel meretasemel ja mägedes kuni 1830 m kõrgusel. Puude eluiga on 200–300 aastat ja need kasvad 10–15 m, harva kuni 30 m kõrguseks.
Mustakuusi (Picea mariana) on Pohjois-Amerikan pohjoisosista kotoisin oleva ainavihanta, pienikokoinen havupuu, joka kuuluu kuusten sukuun ja mäntykasvien heimoon.[2][3] Se on valittu Newfoundlandin provinssipuuksi.[4]
Mustakuusi on hidaskasvuinen pensas tai puu, joka alkaa tuottaa siementä 20 vuoden iässä ja elää tavallisesti 200 vuoden ikäiseksi, mutta joskus jopa 280 vuoden ikäiseksikin.[5] Se kasvaa keskimäärin 9–15 metriä korkeaksi ja rinnankorkeusläpimitaltaan 15–25 senttimetriä paksuksi paitsi levinneisyysalueensa pohjoisreunalla, jossa se jää yleensä 3–6 metriä korkeaksi ja rungoltaan 3–5 senttimetriä paksuksi.[2][5] Suurimmat luonnosta löydetyt yksilöt ovat olleet noin 27 metriä korkeita ja 46 senttimetriä paksuja ja sijainneet Ontarion savimaavyöhykkeellä Kanadassa.[5]
Mustakuusella on lähelle maanpintaa levittäytyvä, laaja juuristo, kapean kartiomainen tai piikkimäinen, tiheähkö latvus sekä lyhyet ja riippuvat haarat, jotka ympäröivät runkoa säännöllisinä kiehkuroina.[2][4][6] Suoraa runkoa peittää karhea, hilseilevä, punertavanharmaa kaarna.[2][3] Kuluvan kesän kasvainranka on ohut, tiheäkarvainen ja vaaleanruskea tai punertava.[4][6] Kärkisilmut ovat harmaanruskeat, pistäväkärkiset ja läpimitaltaan 3 millimetriä.[4] Lehdet ovat himmeitä, sinivihreitä neulasia, jotka siirottavat eri puolille haaraa.[6] Yksittäinen neulanen on 6–15 millimetriä pitkä, tylppäkärkinen, läpileikkaukseltaan neliskulmainen ja kauttaaltaan ilmarakojen peittämä.[4]
Muiden kuusien tapaan mustakuusi on yksikotinen eli samassa yksilössä kasvaa sekä hede- että emikukintoja.[3] Käpymäiset kukinnot syntyvät elokuun alkuun mennessä mutta kehittyvät lopullisesti vasta seuraavan vuoden keväänä.[5] Latvuksen uloimmissa oksissa sijaitsevat hedekukinnot ovat riippuvat, luumunmuotoiset ja 12–20 millimetriä pitkät.[5][7] Ne ovat aluksi tummanpunaiset tai sinipunervat mutta muuttuvat kellanruskeiksi siitepölyn muodostuksen jälkeen.[5][6] Latvuksen kärjessä sijaitsevat emikukinnot ovat pystyt, liereät, 15–25 millimetriä pitkät ja vihreät tai sinipunervat. Ne pölyttyvät touko–kesäkuussa ja kypsyvät nopeasti lähes pallomaisiksi kävyiksi, jotka ovat pituudeltaan 3 senttimetriä ja leveydeltään 2 senttimetriä.[4][5] Ohuiden ja pyöreäkärkisten käpysuomujen alle kehittyy elo–syyskuuhun mennessä ohutkuorisia ja siivekkäitä siemeniä.[3][5][6] Kävyt säilyvät puussa vuosien ajan ja vapauttavat vähitellen siemeniä puun ympäristöön.[5][6]
Mustakuusi on kotoisin laajalta alueelta Pohjois-Amerikan pohjoisosista. Sen levinneisyysalueen pohjoisraja seuraa puurajaa ja kulkee Newfoundlandista Pohjois-Quebeciin ja edelleen Kanadan pohjoisosien halki Alaskan länsirannikolle. Etelässä levinneisyysalue ulottuu Rhode Islandista ja Massachusettsista Minnesotaan ja Brittiläisen Kolumbian keskiosiin. Yksittäisiä esiintymiä on lisäksi Etelä-Wisconsinissa, Etelä-Michiganissa, Pennsylvaniassa ja New Jerseyssä.[2]
Mustakuusi menestyy vähäkalkkisessa ja niukkaravinteisessa maaperässä aina 1 500 metrin korkeuteen asti. Yleensä se kasvaa boreaalisen vyöhykkeen soilla, erityisesti rämeillä ja jokirannoilla, mutta pohjoisempana myös kuivissa kangasmetsissä sekä kalliokoissa.[4][6] Se risteytyy luonnostaan punakuusen kanssa Nova Scotiassa, New Brunswickissa ja Quebecissä, missä lajien levinneisyydet kohtaavat.[2]
Mustakuusen puuaines on vahvaa, suhteellisen kevyttä ja väriltään valkoista tai keltaista.[5] Se on selluloosan tärkein yksittäinen raaka-aine Kanadassa ja taloudellisesti merkittävä paperiteollisuudelle myös Suuria järviä reunustavissa Yhdysvaltojen osavaltioissa, erityisesti Minnesotassa.[2][5] Sitä käytetään myös jonkin verran sahateollisuudessa sekä joulukuusena.[5] Jo ennen teollista käyttöä mustakuusta osattiin hyödyntää monilla tavoilla: sen juurista tehtiin köyttä, pihkasta parantavia voiteita sekä kuusenkerkistä ja neulasista teetä, jolla torjuttiin keripukkia.[2]
Mustakuusi on myös tärkeä ravinnonlähde ja pesäpaikka villieläimille. Se muodostaa merkittävän osan kanadanpyyn ja lumikenkäjäniksen talviravinnosta, ja monet linnut sekä pienet nisäkkäät syövät sen siemeniä. Sen sijaan hirvieläimet ja muut isot nisäkkäät eivät käytä sitä ravintonaan juuri lainkaan.[2]
Mustakuusi (Picea mariana) on Pohjois-Amerikan pohjoisosista kotoisin oleva ainavihanta, pienikokoinen havupuu, joka kuuluu kuusten sukuun ja mäntykasvien heimoon. Se on valittu Newfoundlandin provinssipuuksi.
Picea mariana
L'épinette noire ou épicéa noir ou sapinette noire (Picea mariana), est une espèce de conifère commun au nord-est des États-Unis et surtout au Canada.
C’est une des près de 40 espèces d'épicéas, et l'une des plus résistantes aux climats rudes (taïga) de l’arctique. Elle est pour cette raison le symbole de la forêt boréale d'Amérique, où elle pousse jusqu'à la limite de la toundra.
Elle est parfois victime d'importantes attaques d'insectes défoliateurs, que l'arbre supporte généralement, si elles ne se répètent pas plus de 4 ou 5 ans consécutivement. Les incendies de forêt (naturels ou d'origine humaine) sont un autre facteur de perturbation des peuplements.
L'Épinette noire a un port pyramidal touffu. Elle est buissonnante et tassée (6 à 8 m de haut[réf. nécessaire]) dans les zones où le climat est le plus rude, et arborescente et élancée (20 m de haut[réf. nécessaire]) dans les zones qui lui conviennent, avec des branches de plus en plus tombantes avec l’âge.
Ses rameaux sont rugueux et son écorce écailleuse.
Le cône est petit, de couleur pourpre, virant au brun clair à la maturité.
C’est l’un des conifères les plus répandus de la forêt canadienne, du nord des États-Unis et de l’Alaska[réf. nécessaire]. Il domine la région intérieure de l'Alaska et se raréfie jusqu’à devenir très rare à la limite nord de la forêt boréale. Il est adapté à des milieux relativement extrêmes et pousse aussi bien sur des sols secs, acides et sablonneux que sur des sols tourbeux humides.
L’épinette se reproduit parfois mal par semis (très mal au nord de la toundra, où la diffusion est presque exclusivement assurée par le marcottage naturel de quelques sujets issus de graines apportées par le vent ou des animaux).
La reproduction par marcottage se fait au détriment de la diversité génétique, qui est cependant dans ce cas entretenue par les incendies et épidémies ou attaques d’insectes (Cf. pression sélective). Des études[1] ont montré qu’au niveau mitochondrial, l'épinette noire est effectivement génétiquement très homogène dans la zone subarctique, mais pas au niveau du noyau cellulaire, où elle montre une diversité génétique comparable à celle des forêts boréales plus au sud. Son pollen aéroporté sur de longues distances aurait permis une redistribution des allèles nucléaires des populations boréales jusqu’aux plus nordiques, compensant pour partie la faible diversité génétique du génome mitochondrial marqué par la jeunesse de cette forêt (recolonisation post-glaciaire).
Le fonctionnement des écosystèmes subarctiques, caractérisé par des populations d’arbres comprenant un grand nombre d’individus et un petit nombre d’espèces est encore mal compris, mais il semble que le climat, le feu, et la défoliation périodique par les insectes (comme la tordeuse des bourgeons de l'épinette (TBE) Archips fumiferana), ainsi que la diversité génétique semblent principalement contrôler la répartition de l’épinette et des espèces associées.
Les impacts du réchauffement climatique et de l’extension de la sylviculture et des coupes rases sont également mal compris. Il existe probablement des boucles de rétroactions complexes qui prendront de l’importance, impliquant par exemple les défoliateurs, qui permettent en limitant ou bloquant évapotranspiration de l’épinette d’aider des peuplements entiers à supporter des périodes de sècheresse, tout en limitant le risque d’incendie. Les champignons du sol et les lichens pourraient aussi avoir une grande importance dans l’adaptation des écosystèmes.
Une étude portant sur la recolonisation de sites au nord de l’Alaska a montré que le feu stimulait le recrutement de l'épinette noire, mais avec une faible diversité génétique. La faible croissance de l’espèce dans les zones froides et acides et une faible production de graines viables sont un temps compensé par la longévité des adultes, mais les feux doivent au moins être espacés de 350 ans pour que la population reste stable[2].
Les variations de la sévérité du brûlage du sol (liées au vent, à l’exposition, à l’humidité du sol, au drainage etc.) semblent déterminer différents modèles écopaysagers de régénération. Dans le cas d’une étude faite après des incendies d’intensités diverses dans le centre de l'Alaska, l’épinette noire a été l’espèce dont le semis étaient le plus affecté par les sols les plus dégradés par le feu, alors qu’au contraire le peuplier faux-tremble (Populus tremuloides Michx.) y produisait une biomasse aérienne (g/m2) qui était (7 à 8 ans après des feux) plus de 1000 fois plus élevée que sur les stations où le sol avait été le moins sévèrement brûlé. Là, une combustion faible du sol a favorisé les graminées et les arbustes à feuilles persistantes. Sur les sols les plus fortement brûlés, les feuilles du peuplier et le tapis de mousses acrocarpes pourraient accélérer la restauration de la litière et produire un lit de germination défavorable à une population monospécifique de conifères au profit de peuplements mélangés de conifères dominés par des feuillus[3].
L’épinette noire subsiste généralement dans les forêts boréales, caractérisées par de basses températures annuelles moyennes et de grands contrastes thermiques, marqués par les saisons. Elle est donc adaptée à un apport relativement peu élevé en lumière dû à la courte saison de croissance et à une variation importante du climat[4]. L’épinette s’établit normalement dans des sols mal drainés (donc très humides), où il y a peu d’activités biologiques qui sont effectuées en raison du climat froid[5]. Les conifères contribuent au développement de ce sol, puisque leurs aiguilles au sol forment une litière acide et indigeste pour de nombreux décomposeurs (dû au rapport élevé en C/N de la litière et de sa haute concentration en tanins et polyphénols). La minéralisation s’effectue donc très lentement et c’est pourquoi, en général, il y a dans ces sols une couche épaisse de matière organique[6]. L’épinette noire est donc une espèce dominante dans des domaines climatiques où les conditions sont arides, et s'implante particulièrement bien lorsque la compétition avec d’autres espèces est faible[7].
L’une des adaptations principales de l’épinette noire à ce milieu est sa régénération qui se fait grâce aux feux de forêts, et qui s’effectue de façon cyclique. Ces incendies sont très importants puisqu’ils permettent de régénérer la forêt dans lesquelles les conditions sont de plus en plus difficiles à mesure que cette dernière prend de l’âge. En effet, à mesure que les arbres recouvrent la surface aérienne (ce qui abaisse la température et la luminosité), l’humus au sol devient de plus en plus épais, la qualité du drainage diminue, le sol devient asphyxiant, et les nutriments sont de moins en moins disponibles pour les plantes, incluant pour l’épinette noire. Les feux permettent donc de dégrader l’humus, ce qui rend les nutriments accessibles[4],et favorise l’ouverture des cônes de l’épinette, ce qui permet la dispersion des graines[7].
Au niveau de sa reproduction, l’épinette a également des adaptations qui lui permettent d’être avantagée dans son milieu. C’est une des espèces dominantes du climax de la forêt boréale, c’est-à-dire l’une des espèces qui s’établit en toute fin de succession écologique. Elle produit des graines qui ont la capacité de tolérer l’exposition au soleil, à l’ombre et de résister au gel. Elle peut également se reproduire par multiplication végétative, soit par marcottage, ce qui facilite son établissement sur un humus peu favorable à la germination des graines[7]. L’épinette a également un système racinaire qui n’est pas très profond, ce qui lui permet de croître sur la mince couche de sol qui lui est disponible pour sa croissance, comparativement à d’autres espèces qui ont des racines qui s’établissent profondément dans le sol[7]. L’épinette noire est, au niveau physiologique et comme la plupart des conifères, un exemple d’espèce sempervirente. Ceci implique que cette dernière a développé, au lieu des feuilles, des aiguilles qui sont un compromis à une faible disponibilité en nutriments, à un climat froid et à un faible apport en lumière. Les aiguilles requièrent un investissement énergétique annuel qui est moindre que celui exigé par la formation et la conservation de feuilles, puisqu’elles ont une durée de vie plus longue que ces dernières. Aussi, la photosynthèse peut commencer dès le moment où la température dépasse 4 °C. Ceci permet à l’épinette d’assimiler un maximum de lumière, un avantage dans un milieu où la saison estivale et d’ensoleillement est très courte[4]. La capacité maximale de photosynthèse de l’épinette noire est ainsi réduite par rapport à d’autres végétaux, mais il s’agit d’un compromis lui permettant de l’effectuer efficacement et à partir de peu, dans des conditions où ces autres végétaux ne pourraient subsister.
Comme dans tous les milieux extrêmes, des maladies ou plus souvent des défoliations touchent de vastes peuplements d’arbres. Certaines épinettes se couvrent de lichens après des défoliations et avant des dépérissements. Une colonisation inhabituellement importante de branches d’épinette noire dépérissantes par le lichen bryoria semble être un bon témoin (bioindicateur) du fait que cette partie de l’arbre a antérieurement (jusqu’à 30 ans avant, voire plus) été fortement défoliée par la tordeuse de l'épinette, mais le bryoria n’est pas responsable du dépérissement[8], il a simplement profité de la lumière et peut-être des excrétats de chenilles.
C’est une question de plus en plus étudiée[évasif]. L’augmentation du CO2 et le réchauffement semble pouvoir doper la reproduction par graine et la croissance de l’épinette, sauf à l’extrême nord ou l’espèce est limitée par les vents et par la température estivale trop fraîche, ce qui peut laisser penser que l’enforestation des collines toundriques projetée par certains à la faveur des scénarios « 2 × CO2 » (doublement du taux de CO2 dans l’air) pourrait être plus lente que prévu au nord, où la reproduction par graine échoue généralement au profit du marcottage naturel qui ne permet qu'une très lente colonisation vers le nord.
L’augmentation de la température estivale (somme des degrés-jours) semble un paramètre déterminant[9]. Les modifications des vents au moment de la pollinisation pourraient aussi avoir une certaine importance, de même que les incendies estivaux et l’augmentation de l’enneigement en hiver ou de la pluviométrie au printemps et en automne[10].
Au Canada, son premier usage actuel est l'exploitation, souvent en coupe rase, pour la production de pâte à papier.
L'épinette a été longtemps utilisée pour la charpente (bois solide, disponible, droit, et léger).
L'huile essentielle d'épinette noire est produite par distillation des aiguilles récoltées. L'huile essentielle est principalement constituée des composés suivants acétate de bornyle, alpha-pinènes, camphène, béta-pinènes. Il faut environ 1 kg d'aiguilles pour obtenir 10 ml d'huile essentielle. Cette huile essentielle est principalement reconnue pour ses propriétés tonique, anti-infectieuse et anti-inflammatoire[réf. souhaitée].
On recueille aussi la gomme d'épinette dont on fait une liqueur douce rafraîchissante et effervescente appelée bière d'épinette, un breuvage-maison très usité en Nouvelle-France dès les débuts de la colonie[11].
Picea mariana
L'épinette noire ou épicéa noir ou sapinette noire (Picea mariana), est une espèce de conifère commun au nord-est des États-Unis et surtout au Canada.
C’est une des près de 40 espèces d'épicéas, et l'une des plus résistantes aux climats rudes (taïga) de l’arctique. Elle est pour cette raison le symbole de la forêt boréale d'Amérique, où elle pousse jusqu'à la limite de la toundra.
Elle est parfois victime d'importantes attaques d'insectes défoliateurs, que l'arbre supporte généralement, si elles ne se répètent pas plus de 4 ou 5 ans consécutivement. Les incendies de forêt (naturels ou d'origine humaine) sont un autre facteur de perturbation des peuplements.
Svartgreni (fræðiheiti Picea mariana) er fremur lítið og hægvaxta barrtré upprunið frá Norður-Ameríku. Það hefur svipaða útbreiðslu og hvítgreni en þolir blautan jarðveg. Barrið er smágert og króna trésins er mjó.
Svartgreni getur orðið 15 m hátt á Íslandi en hæstu tré verða um 30 metra í heimkynnum þess.
Svartgreni (fræðiheiti Picea mariana) er fremur lítið og hægvaxta barrtré upprunið frá Norður-Ameríku. Það hefur svipaða útbreiðslu og hvítgreni en þolir blautan jarðveg. Barrið er smágert og króna trésins er mjó.
Svartgreni getur orðið 15 m hátt á Íslandi en hæstu tré verða um 30 metra í heimkynnum þess.
Il peccio nero (Picea mariana (Mill.) Britton, Sterns & Poggenb., 1888) è una specie di peccio, appartenente alla famiglia delle Pinaceae, originaria del Nord America.[1]
Il nome generico Picea, utilizzato già dai latini, potrebbe, secondo un'interpretazione etimologica, derivare da Pix picis = pece, in riferimento all'abbondante produzione di resina.[2] Il nome specifico mariana, secondo una prima interpretazione, significa della Vergine Maria;[3] Una seconda interpretazione, fa riferimento al Maryland, zona peraltro dove la specie non è endemica, ma che nel diciottesimo secolo era creduta essere molto più estesa dai botanici del periodo.[4]
Albero che può raggiungere i 25-30 m di altezza (ma in gran parte del suo areale di solito ridotto a 5-10 m), con tronco monopodiale diritto o ricurvo, che può raggiungere 50-60 cm di diametro; i rami del primo ordine sono generalmente corti e snelli, pendenti. I rami del secondo ordine, anch'essi corti, sono fitti, soprattutto in prossimità della cima. La chioma è variabile ma generalmente stretta, conica, o colonnare, con i rami inferiori che spesso arrivano a terra. I virgulti sono corti e snelli, giallastri o rossastri e ricoperti di una fitta pubescenza nel secondo anno, poi glabri a partire dal terzo anno; i pulvini sono piccoli e lievemente appuntiti.[5]
Le foglie sono aghiformi, di colore verde glauco o verde scuro superiormente, verdi con bande bianco-bluastre inferiormente, lunghe 0,8-1,2 cm, lineari, con sezione rombica e punte pungenti; hanno stomi su entrambe le pagine (1-2 linee su quella superiore, 3-4 linee in quella inferiore). Le gemme vegetative sono ovoidali-coniche, lunghe 5-6 mm, lievemente resinose; hanno perule triangolari, pubescenti, di colore porpora o marrone-purpureo, persistenti per anni.[5]
Sono strobili maschili marroni-giallastri, ascellari e spesso numerosi, lunghi 1-1,5 cm.[5]
I coni femminili sono sessili o obliquamente peduncolati, ovoidali o sub-globulari, spesso a gruppi numerosi e disposti nella parte alta della chioma, lunghi 2-3,5 cm e larghi 1,5-2 cm, inizialmente rossastri o viola-scuro, poi marrone-rosso o porpora-scuro, a volte persistenti per anni prima di cadere a terra. I macrosporofilli sono obovati-sub-orbicolari, inizialmente rigidi poi fragili, con superficie lievemente rugosa, striata e glabra. Le brattee sono rudimentali, ligulate, lunghe 1,2 mm, totalmente incluse. I semi, di color marrone nerastro, sono ovoidali-cuneati e lunghi 2 mm; hanno la parte alata di colore arancione-marrone, ovata, lunga 5-8 mm.[5]
La corteccia è grigia o grigio-nerastra, rugosa e scanalata, con la parti esposte di recente di colore marrone.[5]
Aghi
Cono femminile maturo
Giovani coni femminili
Strobili maschili
Semi
Foresta di pecci neri
Nativo del Canada (Ontario, Nuova Scozia, Territori del Nord-Ovest, Saskatchewan, Yukon, Terranova, Manitoba, Isola del Principe Edoardo, Columbia Britannica, Labrador, Alberta, Québec e Nuovo Brunswick) e degli Stati Uniti d'America (Vermont, Wisconsin, Minnesota, Rhode Island, Alaska, Massachusetts, Maine, New Hampshire, Connecticut, Michigan e Pennsylvania). Vegeta prevalentemente in zone fangose e pantani, a volte caratterizzati dalla presenza di permafrost, dai 150 ai 800 m di quota, con il limite superiore che si alza fino a 1500-1800 m sulle Montagne Rocciose Canadesi; predilige suoli acidi, torbosi. Il clima dell'habitat è freddo, con precipitazioni annue variabili tra 200 e 1400 mm, con stagione vegetativa variabile in durata tra i 25 e i 160 giorni. Si rinviene in formazioni pure nelle zone a torbiera o con permafrost caratterizzate dalla presenza di Sphagnum. Altrove predominano le formazioni miste con Picea laxa, Pinus banksiana e Abies balsamea; nelle zone elevate con Abies lasiocarpa e Pinus contorta e nelle zone ripopolate dopo incendi con Populus tremuloides. Nella parte sud-orientale dell'areale le associazioni più frequenti sono con Chamaecyparis thyoides, Larix laricina, Populus balsamifera, Acer rubrum, Ulmus americana e Fraxinus nigra.[1]
Nel Canada orientale può ibridarsi naturalmente con P. rubens, mentre l'ibridazione con P. glauca non è stata accertata con sicurezza.[6]
Il peccio nero ha una grande importanza economica per lo sfruttamento del suo legno, utilizzato nell'industria cartaria soprattutto nella parte orientale dell'areale. Il legno è leggero e duro, molto chiaro di colore. Seppur in declino, è uno dei pochi pecci nordamericani utilizzati come alberi di Natale, per la chioma con forma compatta in età giovanile. Le proprietà aromatiche di questo peccio vengono sfruttate nella produzione di una sorta di birra, utilizzando gli aghi, mentre i virgulti e le gemme resinose vengono trattati e distillati per ottenere un olio aromatico utilizzato in cosmesi. Vi sono evidenze che una bevanda ricavata dagli aghi, ricca in vitamina c, salvò nel diciottesimo secolo i primi abitanti inglesi insediati nella Baia di Hudson, dalle conseguenze letali dello scorbuto; un altro utilizzo storico e accertato è l'utilizzo delle radici, da parte dei nativi americani, per legare insieme le parti delle canoe realizzate con la corteccia di betulla, sfruttando le loro proprietà elastiche per tenere strette le cuciture. In commercio, inoltre, esistono varie cultivar di questa specie, apprezzata in orticoltura per la sua crescita lenta e compatta, e per il colore della chioma dai particolari riflessi bluastri.[1]
Con un areale vastissimo e una presenza molto numerosa all'interno dello stesso, il peccio nero viene classificato come specie a rischio minimo (least concern in inglese) nella Lista rossa IUCN.[1]
Il peccio nero (Picea mariana (Mill.) Britton, Sterns & Poggenb., 1888) è una specie di peccio, appartenente alla famiglia delle Pinaceae, originaria del Nord America.
Juodoji eglė (lot. Picea mariana, angl. Black Spruce) – pušinių (Pinaceae) šeimos, eglių (Picea) genties visažalis spygliuotis medis. Juodoji eglė yra Niufaundlando ir Labradoro provincijos (Kanada) simbolis.
Plačiai paplitusi Šiaurės Amerikoje (nuo Niufaundlando iki Britų Kolumbijos rytų-vakarų kryptimi, nuo Aliaskos iki Niujorko, Minesotos šiaurės-pietų kryptimi). Sudaro taigos miškus.
Aukštis apie 5-15 m (kartais iki 30 m). Kamieno skersmuo 0,15-0,5 m, kartais 0,6 m. Spygliai 6-15 mm ilgio, melsvai žali. Kankorėžiai cilindriški, 1,5-4 cm ilgio (mažiausi iš visų eglių), 1-2 cm pločio.
Auga įvairiose sąlygose. Pelkėse paprastai juodosios eglės užauga mažesnės. Amžinojo įšalo srityse sudaro „girtus miškus“, kai šaknys neįsitvirtina į dirvą ir medžiai būna pasvirę.
Juodoji eglė (lot. Picea mariana, angl. Black Spruce) – pušinių (Pinaceae) šeimos, eglių (Picea) genties visažalis spygliuotis medis. Juodoji eglė yra Niufaundlando ir Labradoro provincijos (Kanada) simbolis.
Svartgran (vitenskapelig navn Picea mariana) er en art i slekten gran i furufamilien. Svartgrana vokser vilt i Nord-Amerika.
Denne botanikkrelaterte artikkelen er foreløpig kort eller mangelfull, og du kan hjelpe Wikipedia ved å utvide den. Svartgran (vitenskapelig navn Picea mariana) er en art i slekten gran i furufamilien. Svartgrana vokser vilt i Nord-Amerika.
Świerk czarny (Picea mariana (Mill.) Britton, Sterns & Poggenb.) – gatunek drzewa iglastego z rodziny sosnowatych. Rodzimy obszar występowania to Ameryka Północna, gdzie jest gatunkiem pospolitym, a zwarty zasięg jego występowania sięga od gór Wirginii na południu po granicę tundry na Alasce[3]
Jako drzewo ozdobne sadzony jest w parkach i ogrodach. Jest odporny na mróz (strefy mrozoodporności 1-8). Preferuje stanowiska bagienne i słoneczne. Uprawianych jest wiele kultywarów, m.in. karłowa 'Nana'[4].
Świerk czarny (Picea mariana (Mill.) Britton, Sterns & Poggenb.) – gatunek drzewa iglastego z rodziny sosnowatych. Rodzimy obszar występowania to Ameryka Północna, gdzie jest gatunkiem pospolitym, a zwarty zasięg jego występowania sięga od gór Wirginii na południu po granicę tundry na Alasce
Svartgran (Picea mariana) är en trädart med ursprung i Kanada och nordöstra USA. Den klarar av att växa i fuktig och oländig mark och odlas försöksvis i Sverige, men anses ej kunna konkurrera produktionsmässigt med svensk gran på normal skogsmark.[källa behövs]
Wikimedia Commons har media som rör Svartgran.
Svartgran (Picea mariana) är en trädart med ursprung i Kanada och nordöstra USA. Den klarar av att växa i fuktig och oländig mark och odlas försöksvis i Sverige, men anses ej kunna konkurrera produktionsmässigt med svensk gran på normal skogsmark.[källa behövs]
Kara ladin (Picea mariana), çamgiller (Pinaceae) familyasından, Alaska, Kanada ve Amerika Birleşik Devletlerinde Kuzey Amerika taygalarında yetişen, 40-50 5-15 metre boylara ulaşan, 15-50 metre çap yapabilen, dolgun ve düzgün gövdeli, sivri tepeli önemli bir orman ağacı türü. Doğal olarak Picea rubens ile Picea glauca türleriyle melez yapabilir.
Kara ladin (Picea mariana), çamgiller (Pinaceae) familyasından, Alaska, Kanada ve Amerika Birleşik Devletlerinde Kuzey Amerika taygalarında yetişen, 40-50 5-15 metre boylara ulaşan, 15-50 metre çap yapabilen, dolgun ve düzgün gövdeli, sivri tepeli önemli bir orman ağacı türü. Doğal olarak Picea rubens ile Picea glauca türleriyle melez yapabilir.
Країни проживання: Канада (Альберта, Британська Колумбія, Лабрадор, Манітоба, Нью-Брансвік, Ньюфаундленд, Північно-західні Території, Нова Шотландія, Онтаріо, Острови Принца Едуарда, Квебек, Саскачеван, Юкон); США (Аляска, Коннектикут, Мен, Массачусетс, Мічиган, Міннесота, Нью-Гемпшир, Пенсильванія, Род-Айленд, Вермонт, Вісконсин). Росте на болотах. Проживає на висотах від 150 м до 800 м над рівнем моря, іноді в західних горах до 1500 м або 1800 м над рівнем моря, на різних кислих ґрунтах, часто на торфі. Клімат холодний. Річна кількість опадів коливається від 200 до 1400 мм.
В залежності від умов проживання росте як вічнозелене дерево або чагарник до 25 м у висоту і 25 см діаметром (часто набагато менше, виникають криволісся у Полярній Арктиці). Крона вузько конічна. Кора тонка, луската, сіро-бура. Гілки короткі, горизонтальні. Бруньки сіро-коричневі, бл. 3 мм, вершини гострі. Голки 0,6-1,5 (2) см довжиною, від зеленого до блакитно-зеленого кольору, залишаються від 5 до 13 років на дереві. Період цвітіння триває з кінця травня до початку червня. Темно-червоні пилкові шишки довжиною від 12 до 20 міліметрів формуються на периферії крони. Насіннєві шишки 1,5-2,5 (-3.5) см довжиною. 2n = 24. Шишки веретеноподібні, матові, темно-фіолетові, після дозрівання пурпурно-коричневі. Насіння яскраве шоколадно-коричневе без крил близько 2,5 мм в довжину, з крилами близько 10 міліметрів у довжину. Вага зерен від 1,3 до 1,5 грам. Чорна ялина росте дуже повільно, як правило, тільки від 15 до 25 сантиметрів на рік.
Вік 330 років недавно був закріплений для дерева в англ. Sleeping Giant Provincial Park, Онтаріо.
Економічно дуже важливе як джерело деревини, особливо в східних районах.
Загрози не визначені для цьому виду. Зустрічається в багатьох охоронних районах по всьому діапазону поширення.
Це незавершена стаття про родину Соснові.Picea mariana là một loài thực vật hạt trần trong họ Thông. Loài này được (Mill.) Britton, Sterns & Poggenb. miêu tả khoa học đầu tiên năm 1888.[2] Loài này phân bố khắp Canada, được tìm thấy ở tất cả 10 tỉnh và 3 vùng đất vùng cực của Canada. Phạm vi phân bố loài này mở về phía bắc của Hoa Kỳ: ở Alaska, vùng Ngũ Đại Hồ, và Đông Bắc. Loài này thường tạo thành quần xã gọi là rừng taiga hoặc phương bắc.[3][4][5][6][7]
Picea mariana là một loài thực vật hạt trần trong họ Thông. Loài này được (Mill.) Britton, Sterns & Poggenb. miêu tả khoa học đầu tiên năm 1888. Loài này phân bố khắp Canada, được tìm thấy ở tất cả 10 tỉnh và 3 vùng đất vùng cực của Canada. Phạm vi phân bố loài này mở về phía bắc của Hoa Kỳ: ở Alaska, vùng Ngũ Đại Hồ, và Đông Bắc. Loài này thường tạo thành quần xã gọi là rừng taiga hoặc phương bắc.
Picea mariana Mill., Britton, Sterns & Poggenburg
Ареал
Ель чёрная (лат. Picea mariana, Picea nigra) — один из видов ели.
Вид происходит из Северной Америки. Границы естественного ареала — Аляска на западе и Ньюфаундленд на востоке; на севере территория распространения ограничена лесотундрой, на юге — штатами Миннесота и севером Мичигана. Вид встречается также в горных районах Нью-Йорка и в Аппалачских горах Новой Англии. Растёт большей частью в тайге; крайне редко, в южной части ареала, встречается в смешанных лесах[1].
Ель чёрная нетребовательна к климату и почвам и широко распространена на территориях вечной мерзлоты, а в южной части — на сфагновых болотах и влажных низинах.
Вид весьма распространён, охранный статус оценивается как с наиболее низкой угрозой (LC).
Ель чёрная является деревом-символом канадской провинции Ньюфаундленд и Лабрадор.[2]
Ель чёрная представляет собой вечнозелёное хвойное дерево. В зависимости от климатических условий, высота взрослых экземпляров — 7—15 м, диаметр ствола — 15—50 см. В благоприятных условиях встречаются деревья высотой около 30 м. Кора тонкая, серо-коричневая. Хвоя 6—15 мм длиной, сине-зелёная или зелёная. Шишки длиной 2,5—4 см и шириной 1—2 см, одни из наименьших среди елей, от красно-коричневого до фиолетового цвета.[3]
Как декоративные выращиваются в Европе с 1700 года, в России — с середины XIX века.[4] Культивируемые деревья обычно выше, с более пышной кроной, длинной хвоей и крупными шишками. Однако распространена и карликовая форма вида (Picea mariana Nana) высотой около 50 см.[5]
В естественных условиях ель чёрная может создавать гибриды с наиболее близкими видами — с елью красной (Picea rubens) и реже с елью канадской или сизой (Picea glauca).
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검은가문비나무(학명: Picea mariana)는 가문비나무속에 속하는 가문비나무의 일종으로, 캐나다와 미국 북부에 분포한다.
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