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baumier de l'ouest, black cottonwood

big-tooth poplar, bigtooth aspen, grand tremble, large-tooth aspen

Habit Plants to 75 m, 26 dm diam.; moderately heterophyllous. Plants to 35 m, 14 dm diam.; strongly heterophyllous.
Bark

grayish brown, deeply furrowed.

dark grayish brown, furrowed only basally on large trees, (light gray and smooth otherwise).

Branchlets

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

reddish brown, becoming reddish gray by third year, round, 1.3–2.5(–5) mm diam., moderately coarse, thinly tomentose to glabrate.

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 distally flattened at right angle to plane of blade, 1.5–6(–11) cm, 1/2–3/4 blade length;

blade ovate, (2–)4–10(–27.5) × (2–)3–8(–28.5) cm, w/l = 3/4, base broadly cuneate to subcordate, basilaminar glands (1 or) 2(–4), cup-shaped, margins not translucent, not ciliate, apex acute, abaxial surface greenish-white, resin stains absent, (glaucous), densely silky, (hairs white, relatively long, appressed) at emergence, soon becoming glabrate, adaxial bright dark green, glabrous; preformed blade margins coarsely serrate midblade, teeth (1–)5–12(–16) on each side (graded, sharp), sinuses 0.3–4.5(–6) mm deep; neoformed blade margins finely crenate-serrate throughout, teeth (5–)15–50(–138) on each side (rounded), sinuses 0.8–1.5(–2.5) mm deep.

Pedicels

0.5–2.5(–3 in fruit) mm.

0.2–1.5(–2 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 narrowly cup-shaped, obviously oblique, shallowly toothed, 1–2 mm diam.;

stamens 6–12;

anthers truncate;

ovary 2-carpelled;

stigmas 2, filiform, erect.

Capsules

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

narrowly ovoid, 2–5(–6) mm, glabrous, 2-valved.

Seeds

(6–)10–15(–19) per placenta.

(3–)6–8(–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, proximally pubescent, (dull), not evidently resinous;

terminal buds 2.5–7(–10) mm, (glabrous or pubescent); flowering buds separated on branchlets or clustered distally, 6–9(–13) mm.

Catkins

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

floral bract apex deeply cut, not ciliate.

densely (30–)50–150(–175)-flowered, (4–)6–10(–14 in fruit) cm;

floral bract apex deeply cut, ciliate.

2n

= 38.

= 38.

Populus trichocarpa

Populus grandidentata

Phenology Flowering early spring. Flowering Mar–May; fruiting May–Jun.
Habitat Floodplains, lake margins, mesic areas, taluses and other slopes to subalpine tree line Dry to moist, open to closed upland woodlands and forests
Elevation 0-2600(-3000) m (0-8500(-9800) ft) 0-1000 m (0-3300 ft)
Distribution
from FNA
AK; CA; ID; MT; NV; OR; UT; WA; WY; AB; BC; Mexico (Baja California)
[WildflowerSearch map]
from FNA
CT; DC; DE; IA; IL; IN; KY; MA; MD; ME; MI; MN; MO; NC; NH; NJ; NY; OH; PA; RI; TN; VA; VT; WI; WV; MB; NB; NS; ON; PE; QC
[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 grandidentata is a successional species that regenerates after fires by suckering from living rootstocks. The exclusively neoformed leaves on such suckers are much larger than those found on mature trees, are conspicuously pubescent abaxially, and are similar enough to preformed and neoformed leaves of P. heterophylla that they are responsible for incorrect published reports of the latter in upland sites. Once suckers reach their second or third year and begin to branch, they start to bear at least some preformed leaves that clearly identify them as Bigtooth aspen. As far as is known, P. grandidentata and P. heterophylla never grow together at a single site.

Bigtooth aspen hybridizes sporadically with the other native aspen, Populus tremuloides, to form P. ×smithii B. Boivin (synonym P. ×barnesii W. H. Wagner) throughout their large region of sympatry (Frère Marie-Victorin 1930; S. S. Pauley 1956; B. V. Barnes 1961; W. H. Wagner Jr. 1970). Leaves of the hybrids have more numerous, smaller, more rounded teeth than those of P. grandidentata. They may be found as far west as Niobrara River valley, Nebraska, 350 km west of the nearest present station of P. grandidentata.

The related Eurasian white poplar, Populus alba Linnaeus, is commonly and widely planted throughout temperate North America as a pistillate clone with a spreading crown or, less often, as a columnar staminate clone, the Bolleana poplar (‘Pyramidalis’), both of which can persist after cultivation and even spread to a limited extent by root sprouts in old garden sites, roadsides, waste places, hedgerows, and edges of woods. This species differs from P. grandidentata (and all other species of the genus) in having neoformed leaf blades palmately 5-lobed and, along with the petioles, densely white-tomentose abaxially. Unlike all native species of Populus, white poplar has floral bract apices only shallowly cut; these are ciliate like those of native aspens. Populus alba hybridizes commonly with both P. grandidentata, forming P. ×rouleauiana B. Boivin, and P. tremuloides, forming P. ×heimburgeri B. Boivin, in southeastern Canada and the northeastern United States; the hybrids are progressively uncommon southward (E. L. Little Jr. et al. 1957; T. A. Spies and B. V. Barnes 1982). Although their leaves are tomentose abaxially, they differ from P. alba in not having the deeply 5-lobed neoformed leaves. Those of P. ×heimburgeri are shallowly 3-lobed, with apical lobes much larger than lateral ones, and those of P. ×rouleauiana are irregularly and compoundly toothed. With their prominently white-tomentose leaves abaxially, both hybrids are often misidentified as white poplar and are the basis for published reports of naturalized P. alba in sites away from present or former cultivation.

The gray poplar, Populus ×canescens (Aiton) Smith, a natural hybrid between P. alba and the Eurasian aspen, P. tremula Linnaeus, is common and variable in Europe but usually represented by a single pistillate clone in North America. It is widely cultivated, persisting and spreading by root sprouts at former homesites, in waste places, and edges of woods. It is usually less frequent than P. alba, but mostly replaces white poplar in southeastern United States, where it is more widely established under semi-natural conditions. Neoformed leaves have a thin, grayish tomentum abaxially and are irregularly and coarsely toothed rather than 5-lobed, like those of P. alba. Populus ×tomentosa Carrière, from China, is a similar hybrid white poplar with larger leaves and two prominent, cup-shaped basilaminar glands that is rarely planted in southeastern United States in the form of a pistillate clone. It is derived from hybridization between P. alba and a Chinese aspen, P. adenopoda Maximowicz.

Populus alba is similar to P. ×canescens in having resinous winter buds, branchlets and terminal buds that are densely to sparsely tomentose, leaf blade surfaces densely tomentose abaxially when young, retaining their dense tomentum on at least some intervein regions, and usually 5–8(–10) cm. Flowers are similar with discs narrowly cup-shaped, obviously oblique, catkins with floral bracts that are ciliate and apices shallowly cut, 6–12 stamens, the 2 stigmas filiform, and ovaries narrowly ovoid to lanceoloid. Capsules are similar in that they are usually 2-valved, lanceoloid or narrowly ovoid, and 2–7(–9) mm, with seeds (1 or) 2 (or 3) per placenta. The two taxa differ by P. alba having white hairs, neoformed blade margins deeply to shallowly (3 or) 5-lobed, catkin floral bracts densely tomentose, and (1 or) 2 (or 3) seeds per placenta; P. ×canescens has grayish, tannish, or dirty white (tomentose) hairs, neoformed blade margins irregularly toothed, and (3–)5–8 (or 9) seeds per placenta.

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

Source FNA vol. 7, p. 13. FNA vol. 7, p. 20.
Parent taxa Salicaceae > Populus Salicaceae > Populus
Sibling taxa
P. angustifolia, P. balsamifera, P. deltoides, P. fremontii, P. grandidentata, P. heterophylla, P. tremuloides
P. angustifolia, P. balsamifera, P. deltoides, P. fremontii, P. heterophylla, P. tremuloides, P. trichocarpa
Synonyms P. balsamifera subsp. trichocarpa, P. trichocarpa var. ingrata P. tremula subsp. grandidentata
Name authority Torrey & A. Gray: Icon. Pl. 9: plate 878. (1852) Michaux: Fl. Bor.-Amer. 2: 243. (1803)
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