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balsam poplar, balsam poplar (ssp. balsamifera), bam tree, baumier, black cottonwood (ssp. trichocarpa), hackmatack, tacamahaca

Alamo cottonwood, Fremont cottonwood

Habit Plants to 40 m, 21 dm diam.; weakly heterophyllous. Plants to 30 m, 37 dm diam.; strongly heterophyllous, (often 2 or more trunks near base).
Bark

reddish gray, furrowed.

pale tan, deeply furrowed.

Branchlets

reddish brown, becoming grayish brown by third year, round, 1.5–3.5(–5) mm diam., coarse, glabrous or glabrate to densely hairy.

tannish brown, becoming paler tan to bone- white by third year, round, 1–3(–5) mm diam., slender to coarse, glabrous, glabrate, or sparsely to densely hairy, (yellowish).

Leaves

petiole cylindrical or distally slightly flattened in plane of blade, (0.2–)1.5–5 cm, 1/3–1/2 blade length (usually glabrous);

blade usually narrowly ovate to ovate, rarely broadly ovate, (2.5–)5–9(–15) × (0.7–)3–5.5(–9) cm, w/l = 1/2–2/3, base rounded to broadly cuneate or subcordate, basilaminar glands 0 or 2(–5), round, margins not translucent, not ciliate, apex obtuse to acute, abaxial surface often with reddish orange resin stains, glaucous, (veins prominent), adaxial dark green, glabrous; preformed blade margins subentire to very finely, evenly crenate-serrate throughout, teeth (9–)20–35(–45) on each side, sinuses 0.1–0.4 mm deep; neoformed blade margins finely crenate-serrate throughout, teeth (20–)30–45(–60) on each side, sinuses 0.2–0.6 mm deep.

petiole distally flattened at right angle to plane of blade, 1–6(–9) cm, 3/5–3/4 blade length;

blade rhombic-ovate to broadly triangular-ovate, (1.5–)4–8(–14) × (1.5–)3–8(–11) cm, w/l = 3/5–1/1, base cuneate to truncate or cordate, basilaminar glands 0, margins translucent, ciliate, apex short- to long-acuminate, surfaces yellowish green, resin stains not evident, glabrous or densely hairy; preformed blade margins coarsely crenate-serrate midblade, teeth 3–10(–15) on each side (graded, rounded), sinuses (0.2–)0.5–4(–5.5) mm deep; neoformed blade margins finely crenate-serrate much of margin, teeth (10–)20–30(–45) on each side, sinuses 0.1–1 mm deep.

Pedicels

0.5–2(–3.5 in fruit) mm.

1–4(–5.5 in fruit) mm.

Flowers

discs shallowly cup-shaped, not obviously oblique, entire, 2–3(–4) mm diam.;

stamens 20–30;

anthers truncate;

ovary 2-carpelled, ovoid to spherical;

stigmas 2–4, platelike, expanded, reflexed.

discs broadly cup-shaped, not obviously oblique, entire, (2.5–)4–7(–9) mm diam.;

stamens (30–)40–60(–70);

anthers truncate;

ovary 2–4-carpelled, spherical;

stigmas 2–4, flat, platelike, expanded.

Capsules

ovoid, (3–)5–8 mm, glabrous, 2-valved.

spherical, (5–)6–11 mm, glabrous, 2–4-valved.

Seeds

15–22 per placenta.

9–15(–25) per placenta.

Winter

buds reddish, glabrous, resinous (resin red, abundant, very fragrant, balsamic);

terminal buds (8–)12–16(–20) mm; flowering buds clustered distally on branchlets, 15–19 mm.

buds yellow-brown, usually densely stiffly hairy, resinous (resin yellow);

terminal buds (4–)7–11(–14) mm; flowering buds separated on branchlets, (5–)11–18(–22) mm.

Catkins

moderately loosely (35–)50–70(–80)-flowered, 7.5–15(–18 in fruit) cm;

floral bract apex deeply cut, not ciliate.

loosely (10–)15–25(–35)-flowered, (3–)4.5–10(–14 in fruit) cm;

floral bract apex deeply cut, not ciliate.

2n

= 38.

= 38.

Populus balsamifera

Populus fremontii

Phenology Flowering Mar–Jun; fruiting May–Jul.
Habitat Open, rich, low woods, cool, seasonally wet soils, bog margins in boreal forests, aspen parklands, montane streamsides, rocky slopes, gallery forests within tundra
Elevation 0-2900 (-3700) m (0-9500 (-12100) ft)
Distribution
from FNA
AK; CO; CT; DE; IA; IL; IN; MA; ME; MI; MN; MT; ND; NH; NY; OH; PA; SD; VT; WI; WV; WY; AB; BC; MB; NB; NF; NS; NT; NU; ON; PE; QC; SK; YT; SPM
[WildflowerSearch map]
[BONAP county map]
from FNA
AZ; CA; ID; NM; NV; TX; UT; n Mexico
[WildflowerSearch map]
Discussion

Populus balsamifera has been reported in error from Nebraska based on incorrectly localized specimens and from Idaho, Oregon, and Utah based on vegetative specimens of P. trichocarpa or intergrades. The two species can be difficult to separate vegetatively, particularly in their region of overlap and hybridization along the northern Cordilleran axis from southern Alaska to northwestern Wyoming. Their hybrids, named P. ×hastata Dode, have intermediate leaf shapes and also differ from P. balsamifera in having capsules with 2–4 sparsely hairy or glabrous valves (T. C. Brayshaw 1965). Populus balsamifera also hybridizes and intergrades with another native species of sect. Tacamahaca, P. angustifolia, to form P. ×brayshawii B. Boivin where the margins of their ranges overlap (Brayshaw 1965b). Populus ×brayshawii is intermediate in some respects between its parents. It is most similar to P. angustifolia; it differs in longer petioles and darker twigs, characteristics in which it approaches P. balsamifera. Some trees of P. balsamifera from North Dakota (Bottineau and Divide counties) also seem to show an influence of P. angustifolia, although they are far from the present range of the latter species.

Populus ×jackii Sargent (synonyms P. ×andrewsii Sargent, P. ×bernardii B. Boivin, P. ×dutillyi Lepage, and P. ×gileadensis Rouleau) is an intersectional hybrid with P. deltoides (sect. Aigeiros) and is moderately common in riparian and other wet habitats throughout the broad range of overlap between these two species (Alberta, Colorado, Illinois, Indiana, Iowa, Manitoba, Massachusetts, Michigan, Minnesota, Montana, Nebraska, New York, North Dakota, Ontario, Quebec, Pennsylvania, Saskatchewan, South Dakota, West Virginia, and Wisconsin) (W. G. Ronald et al. 1973; J. E. Eckenwalder 1984). A pistillate clone that probably arose from this hybrid by segregation or backcrossing (‘Balm-of-Gilead’) has been widely cultivated since at least the eighteenth century for its bud resin, used in treating coughs (E. Rouleau 1948). Capsules rarely, if ever, mature and trees do not appear to produce fertile seed, but persist and spread by root sprouts in waste places and at edges of woods. It is cultivated mostly in southeastern Canada and eastern United States to the Great Plains, chiefly in mountains in southeastern United States. This clone is more balsam poplarlike than first generation hybrids and has differences from wild hybrids in North America. It may have arisen in Europe through hybridization and backcrossing between P. balsamifera and southern P. deltoides subsp. deltoides. Most wild hybrids have P. deltoides subsp. monilifera as the cottonwood parent.

Similar to the other North American balsam poplars, Populus balsamifera hybridizes sporadically with the introduced Eurasian P. nigra. That hybrid, P. ×rollandii Rouleau, which was originally thought to have involved P. ×canadensis, itself a hybrid offspring of P. nigra, has been collected in the vicinity of Montreal, Quebec (E. Rouleau 1944). Its leaves are similar in shape to those of P. ×canadensis but have the reddish resin stains and cylindrical petioles of P. balsamifera.

Populus balsamifera does not hybridize naturally with P. tremuloides, as sometimes reported (E. Lepage 1961; F. G. Bernard 1968). Specimens that formed the basis for those reports are either P. ×jackii or slender sucker shoots of P. tremuloides bearing correspondingly narrow leaves.

Populus ×jackii has branchlets that are short-haired or pubescent, petioles densely pubescent, at least distally, preformed blade margins with 20(–45) teeth on each side, sinuses to 1.5 mm deep, pedicels to 3 mm, discs saucer-shaped, 1–4 mm diam., ovaries 3- or 4-carpelled and glabrous, capsules usually 3- or 4-valved, ovoid, (4–)8–11(–16) mm, and seeds (6 or) 7–15(–25) per placenta. It is similar to P. simonii in having winter buds with red resin, petioles to 2 cm, round, cylindrical, or distally slightly flattened in the plane of blade, leaf blades lighter green abaxially, elliptic-rhombate to ovate, (1–)3–20(–27.5) cm, bases acute, cuneate, rounded, truncate, or shallowly cordate, apices obtuse, acute, or acuminate, and surfaces not obviously resin-stained, with abaxial surface glabrous or with short, stiff hairs. The flowers are similar with discs entire, persistent, and not obviously oblique, catkins with floral bracts not ciliate and glabrous abaxially, 10–60(–70) stamens (P. simonii with fewer than 12), anthers usually truncate, stigmas 2–4 and expanded, and ovaries ovoid to spherical. In addition to these traits, P. simonii has terminal buds that are usually less than 12 mm, branchlets whitish tan by the third year, catkins 3–8 cm, and stamens usually fewer than 12.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Subspecies 2 (2 in the flora).

Populus fremontii hybridizes with P. deltoides subsp. wislizeni where they come in contact in the Colorado Plateau region and trans-Pecos Texas. Hybrids have longer pedicels and narrower discs than does P. fremontii, and less densely hairy twigs in regions where P. fremontii is densely pubescent. It also hybridizes with the two members of sect. Tacamahaca with which it overlaps, P. trichocarpa (P. ×parryi Sargent), and P. angustifolia (P. ×hinckleyana Correll) (synonyms P. ×acuminata Rydberg nothomorph rehderi Sargent and P. ×intercurrens S. Goodrich & S. L. Welsh). Both hybrids have smaller, more numerous teeth on preformed leaves than does P. fremontii, with blades clearly paler abaxially than adaxially, and buds with reddish resin (J. E. Eckenwalder 1984). Preformed leaves are broadly ovate to heart-shaped in P. ×parryi (Eckenwalder 1984b) and usually ovate in P. ×hinckleyana; trees from the type locality in the Davis Mountains, Texas, had round leaves (D. S. Correll 1960). They could be distinguished from P. ×parryi by their smaller leaf blades and hairy petioles. Trees of P. ×parryi have been found in Mohave County, Arizona, east of the present range of P. trichocarpa (Eckenwalder 1992).

Populus ×inopina Eckenwalder is a hybrid between P. fremontii and P. nigra known only from the type locality along Coyote Creek, San Jose, California, where P. nigra was the seed parent (J. E. Eckenwalder 1982). Trees of the same parentage were produced artificially by A. B. Stout and E. J. Schreiner (1933); none appears to have survived. They differ from P. nigra in broader habit, twigs thicker, buds thicker and less red, broader and more cordate leaves with larger teeth, and more numerous stamens. They differ from P. fremontii in narrower habit, twigs more orange, buds without a green cast, longer leaf apices, more numerous teeth, and fewer stamens. If pistillate trees occur, they would be expected to have 2 or 3 carpels and discs 3–5 mm diam., both intermediate between those of the parents.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Key
1. Neoformed blade: usually about as wide as long, rarely wider, bases truncate or cordate, apices short-acuminate; branchlets glabrous or glabrate to densely hairy.
subsp. fremontii
1. Neoformed blade: longer than wide, bases cuneate or truncate, apices long-acuminate; branchlets usually densely hairy.
subsp. mesetae
Source FNA vol. 7, p. 14. FNA vol. 7, p. 19.
Parent taxa Salicaceae > Populus Salicaceae > Populus
Sibling taxa
P. angustifolia, P. deltoides, P. fremontii, P. grandidentata, P. heterophylla, P. tremuloides, P. trichocarpa
P. angustifolia, P. balsamifera, P. deltoides, P. grandidentata, P. heterophylla, P. tremuloides, P. trichocarpa
Subordinate taxa
P. fremontii subsp. fremontii, P. fremontii subsp. mesetae
Synonyms P. balsamifera var. subcordata, P. candicans, P. tacamahacca
Name authority Linnaeus: Sp. Pl. 2: 1034. (1753) S. Watson: Proc. Amer. Acad. Arts 10: 350. (1875)
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