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baumier de l'ouest, black cottonwood

Alamo cottonwood, Fremont cottonwood

Habit Plants to 75 m, 26 dm diam.; moderately heterophyllous. Plants to 30 m, 37 dm diam.; strongly heterophyllous, (often 2 or more trunks near base).
Bark

grayish brown, deeply furrowed.

pale tan, deeply furrowed.

Branchlets

reddish brown, becoming gray by third year, round, 1.5–3(–7) mm diam., coarse, usually 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 (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, 1–6(–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

0.5–2.5(–3 in fruit) mm.

1–4(–5.5 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 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

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

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

Seeds

(6–)10–15(–19) per placenta.

9–15(–25) 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 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

densely (10–)25–50(–90)-flowered, (4.5–)7–10(–17 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 trichocarpa

Populus fremontii

Phenology Flowering early spring.
Habitat Floodplains, lake margins, mesic areas, taluses and other slopes to subalpine tree line
Elevation 0-2600(-3000) m (0-8500(-9800) ft)
Distribution
from FNA
AK; CA; ID; MT; NV; OR; UT; WA; WY; AB; BC; Mexico (Baja California)
[WildflowerSearch map]
from FNA
AZ; CA; ID; NM; NV; TX; UT; n Mexico
[WildflowerSearch 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.)

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. 13. FNA vol. 7, p. 19.
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. grandidentata, P. heterophylla, P. tremuloides, P. trichocarpa
Subordinate taxa
P. fremontii subsp. fremontii, P. fremontii subsp. mesetae
Synonyms P. balsamifera subsp. trichocarpa, P. trichocarpa var. ingrata
Name authority Torrey & A. Gray: Icon. Pl. 9: plate 878. (1852) S. Watson: Proc. Amer. Acad. Arts 10: 350. (1875)
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