The green links below add additional plants to the comparison table. Blue links lead to other Web sites.
enable glossary links

baumier de l'ouest, black cottonwood

liard amer, mountain cottonwood, narrow-leaf cottonwood, willow-leaf poplar

Habit Plants to 75 m, 26 dm diam.; moderately heterophyllous. Plants to 20 m, 7 dm diam.; moderately heterophyllous.
Bark

grayish brown, deeply furrowed.

light brown, shallowly furrowed.

Branchlets

reddish brown, becoming gray by third year, round, 1.5–3(–7) mm diam., coarse, usually densely hairy.

orange-brown, becoming whitish tan by third year, round or 5-angled, 1.5–2.5(–3.5) mm diam., not coarse, glabrous.

Leaves

petiole cylindrical or distally slightly flattened in plane of blade (often markedly swollen distally), 1–5(–9.5) cm, 1/2 blade length, (glabrous or sparsely pubescent);

blade usually triangular-ovate or narrowly ovate to cordate, (3–)5–9(–15) × (1–)2.5–6(–10) cm, w/l = 1/2–2/3, base rounded to cordate, basilaminar glands 0–2, round, margins not translucent, not ciliate, apex obtuse to acute, abaxial surface white to grayish white or greenish white with red resin stains, sparsely pubescent, adaxial dark green, glabrous; preformed blade margins very finely, evenly crenate-serrate throughout, teeth (20–)35–40(–50) on each side, sinuses 0.1–0.4 mm deep; neoformed blade margins finely, evenly crenate-serrate throughout, teeth (25–)40–60 on each side, sinuses 0.2–0.6 mm deep.

petiole round, adaxially slightly channeled distally, 0.2–0.8(–1.7) cm, 1/8–1/5 blade length, (glabrous);

blade usually lanceolate to narrowly ovate, (1.5–)4–8(–13.5) × 0.8–2.5(–4) cm, w/l = 1/5–1/2, base acute to rounded, basilaminar glands 0, margins not translucent, not ciliate, apex acute, abaxial surface whitish green, weakly glaucous, adaxial dark green, glabrous; preformed blade margins subentire to minutely, evenly crenate-serrate throughout, teeth (14–)23–35(–65) on each side, sinuses 0.1–0.3 mm deep; neoformed blade margins finely crenate-serrate throughout, teeth 35–65(–80) on each side, sinuses 0.1–0.6(–1.5) mm deep.

Pedicels

0.5–2.5(–3 in fruit) mm.

0.5–1.5(–3 in fruit) mm.

Flowers

discs broadly cup-shaped, not obviously oblique, entire, 4–6 mm diam.;

stamens 30–50(–60);

anthers truncate;

ovary 3- or 4-carpelled, spherical, (hairy);

stigmas 2–4, platelike, expanded, spreading.

discs shallowly cup-shaped, not obviously oblique, entire, 1–1.5(–3) mm diam.;

stamens 10–20;

anthers truncate;

ovary 2-carpelled, ovoid to spherical;

stigmas 2–4, broad, expanded.

Capsules

spherical, (6–)7–9 mm, densely hairy to glabrate, 3- or 4-valved.

broadly ovoid to spherical, 3–5 mm, glabrous, 2-valved.

Seeds

(6–)10–15(–19) per placenta.

(2–)4–7(–9) per placenta.

Winter

buds red, sparsely hairy or glabrous, resinous (resin red, abundant, very fragrant);

terminal buds 8–15(–20) mm; flowering buds clustered distally on branchlets, 18–20 mm.

buds reddish brown, glabrous, resinous (resin red, fragrant);

terminal buds (3–)6–9(–13) mm; flowering buds clustered distally on branchlets, 8–12(–18) mm.

Catkins

densely (10–)25–50(–90)-flowered, (4.5–)7–10(–17 in fruit) cm;

floral bract apex deeply cut, not ciliate.

± densely 35–50-flowered, 3–8(–9 in fruit) cm;

floral bract apex deeply cut, not ciliate.

2n

= 38.

= 38.

Populus trichocarpa

Populus angustifolia

Phenology Flowering early spring. Flowering Apr–May; fruiting Jun–Jul.
Habitat Floodplains, lake margins, mesic areas, taluses and other slopes to subalpine tree line Streamsides in mountains and foothills
Elevation 0-2600(-3000) m (0-8500(-9800) ft) 1500-2400(-3300) m (4900-7900(-10800) ft)
Distribution
from FNA
AK; CA; ID; MT; NV; OR; UT; WA; WY; AB; BC; Mexico (Baja California)
[WildflowerSearch map]
from FNA
AZ; CO; ID; MT; NE; NM; NV; SD; TX; UT; WY; AB; SK; Mexico (Chihuahua, Coahuila, Sonora)
[WildflowerSearch map]
[BONAP county map]
Discussion

Populus trichocarpa has been mistakenly reported from North Dakota based on specimens of P. ×jackii (P. balsamifera × P. deltoides). It hybridizes with P. balsamifera to form P. ×hastata Dode along the northern Rocky Mountain axis (Alaska, Alberta, British Columbia, and Idaho). Hybrids have capsules with 2–4 glabrous or sparsely hairy valves. The extent of hybridization has led to treatment of P. trichocarpa as a subspecies of P. balsamifera (T. C. Brayshaw 1965; L. A. Viereck and J. M. Foote 1970); these two balsam poplars are more closely related to Asian members of sect. Tacamahaca than they are to each other (J. E. Eckenwalder 1996). Mountain ranges of the Intermountain Region (California, Idaho, Nevada, Oregon, and Utah) have trees intermediate between P. trichocarpa and P. angustifolia. These hybrids have narrower leaves with shorter petioles and sparsely hairy capsules with 2–3 valves.

In addition to hybridizing with other North American species of sect. Tacamahaca, Populus trichocarpa also hybridizes with both native species of sect. Aigeiros. Populus ×generosa A. Henry (synonym P. ×interamericana van Broekhuizen), a hybrid between P. trichocarpa and P. deltoides, is rare in the far western area of the range for P. deltoides subsp. monilifera, where it overlaps with the more drought-tolerant inland P. trichocarpa (Idaho, Montana, Washington, and Wyoming) (J. E. Eckenwalder 1984). This hybrid has also been grown artificially, and such hybrids between coastal P. trichocarpa and P. deltoides subsp. deltoides are becoming increasingly important plantation trees in the Pacific Northwest from northern Oregon to British Columbia, as well as in Europe. They are perhaps the fastest growing of all poplars in volume, with the rapid height growth of P. trichocarpa added to the steady diameter growth of P. deltoides (R. F. Stettler et al. 1988).

Populus ×parryi Sargent, a hybrid between P. trichocarpa and P. fremontii, is commonly found in a wide variety of mesic habitats throughout the region of sympatry between its parents in California and Nevada (and beyond the range of P. trichocarpa in Mohave County, Arizona; J. E. Eckenwalder 1992). It can be found particularly in canyons where its parents are elevationally separated but overlap as permanent streams spill out into lower elevations (Eckenwalder 1984, 1984b). A morphologically and ecologically distinctive race of P. trichocarpa in coastal southern California with heart-shaped leaves may have arisen through this kind of hybridization (Eckenwalder 1984c). This race includes the type of P. trichocarpa from Ventura County.

Populus maximowiczii A. Henry is an Asian balsam poplar that is sometimes cultivated as an ornamental, but usually as a plantation tree or parent of plantation hybrids. It is distinguished from P. trichocarpa and P. balsamifera by its elliptic leaves with rugose adaxial surfaces.

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

Populus angustifolia has been mistakenly reported from eastern California and eastern Oregon based on intergrades with, and narrow-leaved specimens of, P. trichocarpa in those arid regions. It is a characteristic species of the Rocky Mountains, extending onto the plains and overlapping in canyon mouths as they exit the mountains with two North American species of sect. Aigeiros, P. deltoides and P. fremontii, and hybridizing with each of them. It also hybridizes with the other two native species of sect. Tacamahaca, P. balsamifera and P. trichocarpa. The hybrid with P. balsamifera, P. ×brayshawii B. Boivin, differs most obviously in longer petioles, at least 2.5 cm, and is increasingly common from Colorado northwards, largely replacing P. angustifolia in southern Alberta (T. C. Brayshaw 1965b; S. B. Rood et al. 1985). The hybrid with P. trichocarpa (unnamed) is uncommon and largely confined to the Great Basin region, including Montana (W. W. White 1951). Populus angustifolia does not hybridize naturally with P. tremuloides, as sometimes reported (B. Boivin 1966b). The specimens that formed the basis for that report are long shoots of P. angustifolia with relatively coarsely toothed neoformed leaves.

Populus ×acuminata Rydberg is the intersectional hybrid of P. angustifolia with P. deltoides (sect. Aigeiros) that occurs on floodplains of major streams, primarily along the foot of the Rocky Mountain Front Ranges where these species grow together, but also extends onto the plains and Colorado Plateau (Alberta, Arizona, Colorado, Montana, Nebraska, New Mexico, North Dakota, South Dakota, Texas, Utah, and Wyoming) (J. E. Eckenwalder 1984). As with other cloning hybrids, it can often occur without one or both parents. It differs from P. angustifolia in larger, ovate leaves with coarser teeth, less color differentiation between abaxial and adaxial surfaces, and longer petioles that are slightly flattened side to side near the junction with the blade. Because of its frequency and morphological consistency, P. ×acuminata was first described as a species and is often treated as such in local and regional floras. It was long suspected of being a hybrid, and its hybrid origin was amply confirmed by multiple lines of evidence in the 1970s and 1980s (D. J. Crawford 1974; A. G. Jones and D. S. Seigler 1975; S. B. Rood et al. 1985). The name has also been widely misapplied to intersectional hybrids involving other combinations of balsam poplar and cottonwood parents (Eckenwalder).

Populus ×berolinensis Dippel is a similar cultivated, introduced, intersectional hybrid between two Eurasian species, P. laurifolia Ledebour (sect. Tacamahaca) and P. nigra Linnaeus (sect. Aigeiros). It has an upright growth habit and leaves similar in shape to those of P. ×acuminata, but more balsam poplar-like with smaller teeth and greater color differentiation between abaxial and adaxial surfaces. Pistillate individuals may hybridize with native species of both parent sections (W. G. Ronald and J. W. Steele 1974).

Populus ×hinckleyana Correll (synonyms P. ×acuminata nothomorph rehderi Sargent and P. ×intercurrens S. Goodrich & S. L. Welsh) is the intersectional hybrid of P. angustifolia with P. fremontii (sect. Aigeiros) and is moderately common in canyons throughout their range of sympatry (Arizona, Idaho, Nevada, New Mexico, Texas, Utah, and Mexico [Chihuahua, Sonora]). At the type locality in the Davis Mountains, Texas, P. angustifolia is now absent, and the cottonwood parent is P. fremontii subsp. mesetae, but other occurrences have arisen through hybridization with P. fremontii subsp. fremontii (G. C. Bennion et al. 1961; J. E. Eckenwalder 1984; P. Keim et al. 1989). It differs from P. angustifolia in hairy young shoots and a broader floral disc.

A related Eurasian species, Populus simonii Carrière, is moderately commonly cultivated, especially in the form of a broadly pyramidal staminate clone (‘Pyramidalis’). It shares the slender, often 5-angled twigs and relatively small leaves of P. angustifolia, but differs most noticeably in elliptic blades of preformed leaves and obovate blades of neoformed leaves.

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

Source FNA vol. 7, p. 13. FNA vol. 7, p. 16.
Parent taxa Salicaceae > Populus Salicaceae > Populus
Sibling taxa
P. angustifolia, P. balsamifera, P. deltoides, P. fremontii, P. grandidentata, P. heterophylla, P. tremuloides
P. balsamifera, P. deltoides, P. fremontii, P. grandidentata, P. heterophylla, P. tremuloides, P. trichocarpa
Synonyms P. balsamifera subsp. trichocarpa, P. trichocarpa var. ingrata P. ×sennii, P. tweedyi
Name authority Torrey & A. Gray: Icon. Pl. 9: plate 878. (1852) E. James: Account Exped. Pittsburgh 1: 497. (1823)
Web links