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gray willow, large gray or gray willow, large gray willow

polished willow, red willow

Habit Shrubs, 3–7 m. Stems: branches brownish, not glaucous, pilose, villous, or tomentose to glabrescent, (peeled wood with striae to 62 mm); branchlets yellow-brown, pilose, velvety, or densely villous. Trees, 2–15 m. Stems: branches flexible to highly brittle at base, gray-brown to yellow-brown, glabrous or villous; branchlets yellow-brown or red-brown, glabrous, densely villous, velvety, or pilose, nodes hairy.
Leaves

stipules rudimentary or foliaceous on early ones, foliaceous on late ones, apex acute or rounded;

petiole convex to flat adaxially, 4–15 mm, tomentose adaxially;

largest medial blade elliptic, broadly elliptic, oblanceolate, or obovate, 65–105 × 22–52 mm, 2–3 times as long as wide, base convex or cuneate, margins slightly revolute, entire, crenate, or sinuate, (glands submarginal), apex acuminate or convex, abaxial surface glaucous, tomentose, hairs erect or spreading, curly, adaxial dull or slightly glossy, pubescent or tomentose;

proximal blade margins entire;

juvenile blade yellowish green, sparsely to densely tomentose abaxially, hairs white.

stipules rudimentary grading into foliaceous or absent on early ones, usually foliaceous on late ones, apex acute, acuminate, rounded or convex;

petiole (shallowly or deeply grooved adaxially, margins sometimes touching, sometimes with basilaminar glands, thickening), 3.5–18 mm, pubescent to glabrescent adaxially;

largest medial blade lorate, narrowly oblong, narrowly elliptic, lanceolate, or obovate, 53–190 × 11–35 mm, 2.8–9 times as long as wide, base convex, subcordate, rounded, or cuneate, margins crenate, entire, or finely serrulate, apex acuminate, acute, or caudate, abaxial surface glabrous or pubescent, hairs spreading, white and/or ferruginous, adaxial highly or slightly glossy, glabrous or pubescent, midrib sometimes villous;

proximal blade margins entire;

juvenile blade glabrous or moderately densely long-silky to pilose abaxially, hairs white and/or ferruginous.

Staminate flowers

adaxial nectary oblong or ovate, 0.5–1 mm;

filaments distinct, glabrous or hairy basally;

anthers yellow or purple turning yellow, ellipsoid or shortly cylindrical, 0.7–1 mm.

abaxial nectary 0.4–0.6 mm, adaxial nectary oblong, square, or ovate, 0.3–0.6 mm, nectaries distinct;

stamens 3–7;

filaments (sometimes basally connate), hairy on proximal 1/2 or basally;

anthers 0.4–0.6 mm.

Pistillate flowers

adaxial nectary oblong or square, 0.4–1 mm, shorter than stipe;

stipe 1.2–2.7 mm;

ovary pyriform, long-silky, beak slightly bulged below styles;

ovules 12 per ovary;

styles 0.2–0.5 mm;

stigmas slenderly or broadly cylindrical, 0.3–0.6 mm.

adaxial nectary square, 0.2–0.6 mm;

stipe 1.4–2.8 mm;

ovary pyriform, obturbinate, or ellipsoidal, beak slightly bulged below styles;

ovules 12–24 per ovary;

styles 0.1–0.2 mm;

stigmas 0.2–0.23–0.28 mm.

Capsules

5–5.6 mm.

3–5.5 mm.

Catkins

flowering before leaves emerge; staminate stout or subglobose, 26–39 × 12–26 mm, flowering branchlet 0–5 mm; pistillate densely flowered, stout or subglobose, 27–54(–75 in fruit) × 4–15 mm, flowering branchlet 1–5(–10) mm;

floral bract dark brown, black, or bicolor, 2–3 mm, apex acute or convex, abaxially hairy, hairs straight.

staminate 31–83 × 7–13 mm, flowering branchlet 2–26 mm; pistillate 28–79 × 6–11 mm, flowering branchlet 3–14 mm;

floral bract 1.6–3.4 mm, apex rounded or acute, irregularly toothed or entire, abaxially sparsely to moderately densely hairy proximally or throughout, hairs wavy; pistillate bract deciduous after flowering.

2n

= 76.

Salix cinerea

Salix laevigata

Phenology Flowering mid Mar-late May. Flowering (Dec-)Feb or mid Apr-early Jun.
Habitat Stream shores, mesic woodlands, gravelly or sandy beaches, waste ground Riparian forests along streams, seepage areas, springs, subalkaline or brackish lakeshores, canyons, ditches
Elevation 0-700 m (0-2300 ft) 0-2200 m (0-7200 ft)
Distribution
from FNA
AL; CT; DC; GA; IA; KY; LA; MA; MD; MI; MO; NC; NJ; NY; OH; PA; RI; SC; SD; TN; UT; VA; WI; WV; ON; Eurasia [Introduced in North America]
[WildflowerSearch map]
[BONAP county map]
from FNA
AZ; CA; NV; OR; UT; Mexico (Baja California, Baja California Sur)
[WildflowerSearch map]
[BONAP county map]
Discussion

The Ohio occurrence of Salix cinerea is based on information from T. Cooperrider (pers. comm.).

Salix cinerea and S. atrocinerea are very closely related. Their occurrence in the flora area, as naturalized introductions, is not well understood, probably because they usually are introduced under the name S. caprea, and that species often is not treated in North American floristic literature (e.g., C. K. Schneider 1921; M. L. Fernald 1950). They probably are introductions of long-standing brought to the New World for their value as ornamentals and bee-plants. Salix atrocinerea was first documented in the southeastern United States (G. W. Argus 1986) after plants with ferruginous hairs and prominently striate wood were found in North Carolina; since that time, it has been found in other states and provinces. In the northeastern states, S. atrocinerea and S. cinerea are thought to be invasive species. The species do reproduce by seed and hundreds of seedlings were observed in a drained reservoir (A. Zinovjev, pers. comm.) and on sandy pond shores (T. Rawinski, pers. comm.), where they are thought to compete with native species.

The presence of long, prominent, striae on the peeled wood of 4–5 year old branches is commonly used in European literature (K. H. Rechinger 1993; A. K. Skvortsov 1999) to separate Salix cinerea and S. atrocinerea from S. caprea etc., in which the wood is smooth or with fewer, shorter striae. In the flora area, long striae also occur in S. bebbiana, S. discolor, and S. humilis, but usually they are not as long as or as prominent in S. cinerea and S. atrocinerea. Some floras (e.g., F. Martini and P. Paiero 1988) use the relative prominence of striae to separate S. cinerea and S. atrocinerea, but their separation remains difficult. The presence of ferruginous hairs on the leaves of S. atrocinerea is the best diagnostic characteristic, but they are not always present or easily observed. For a comparison of these species, see the key to species under subg. Vetrix. For further discussion of morphologies, see Salix ×smithiana Willdenow [p. 132] and 76. S. discolor.

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

Hybrids:

Salix laevigata forms natural hybrids with S. gooddingii.

Related Species:

Salix humboldtiana Willdenow: Humboldt willow is not known to occur in the flora area. It is characterized by: trees, 4–25 m; branches highly brittle at base, bud-scale margins distinct and overlapping adaxially; stipules on late leaves rudimentary or foliaceous; largest medial leaf blade usually linear, abaxial surface not glaucous, adaxial dull; pistillate bract deciduous after flowering; stamens 3–7; capsules with distinct, often raised, white veins. It occurs throughout much of Mexico to central Chile.

Salix humboldtiana is closely related to S. nigra in its generally narrow leaf blades, which are not glaucous abaxially. The two differ in the following characters: S. humboldtiana has leaf blades linear to sometimes narrowly oblong (10–28.6 times as long as wide), ovaries usually ovoid to ellipsoid, ovary walls often stomatiferous and with raised, white veins, and capsule valves relatively thick, slightly recurved. S. nigra has leaf blades usually narrowly lanceolate (6–13 times as long as wide), ovaries pyriform to obclavate, ovary walls neither stomatiferous nor notably veined, and capsule valves relatively thin and strongly recurved. Both species occur in Chihuahua, Mexico.

The report by R. I. Lonard et al. (1991) that specimens identified as Salix nigra from the lower Rio Grande, Texas, resemble S. humboldtiana in having strongly veined capsules suggests that S. humboldtiana, or intergrades with that species, may occur in Texas. Attempts to locate a voucher specimen were unsuccessful; because strongly veined capsules are diagnostic, further field study is indicated.

An earlier name, Salix chilensis Molina, has been applied to this species; it does not seem to pertain to this taxon (C. K. Schneider 1918).

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

Source FNA vol. 7, p. 132. FNA vol. 7, p. 34.
Parent taxa Salicaceae > Salix > subg. Vetrix > sect. Cinerella Salicaceae > Salix > subg. Protitea > sect. Humboldtianae
Sibling taxa
S. alaxensis, S. alba, S. amygdaloides, S. arbusculoides, S. arctica, S. arctophila, S. argyrocarpa, S. arizonica, S. athabascensis, S. atrocinerea, S. aurita, S. babylonica, S. ballii, S. barclayi, S. barrattiana, S. bebbiana, S. bonplandiana, S. boothii, S. brachycarpa, S. breweri, S. calcicola, S. candida, S. caprea, S. caroliniana, S. cascadensis, S. chamissonis, S. chlorolepis, S. columbiana, S. commutata, S. cordata, S. daphnoides, S. delnortensis, S. discolor, S. drummondiana, S. eastwoodiae, S. elaeagnos, S. eriocephala, S. euxina, S. exigua, S. famelica, S. farriae, S. floridana, S. fuscescens, S. geyeriana, S. glauca, S. gooddingii, S. hastata, S. herbacea, S. hookeriana, S. humboldtiana, S. humilis, S. interior, S. irrorata, S. jejuna, S. jepsonii, S. laevigata, S. lasiandra, S. lasiolepis, S. lemmonii, S. ligulifolia, S. lucida, S. lutea, S. maccalliana, S. melanopsis, S. monochroma, S. monticola, S. myricoides, S. myrsinifolia, S. myrtillifolia, S. nigra, S. niphoclada, S. nivalis, S. nummularia, S. orestera, S. ovalifolia, S. pedicellaris, S. pellita, S. pentandra, S. petiolaris, S. petrophila, S. phlebophylla, S. planifolia, S. polaris, S. prolixa, S. pseudomonticola, S. pseudomyrsinites, S. pulchra, S. purpurea, S. pyrifolia, S. raupii, S. reticulata, S. richardsonii, S. rotundifolia, S. scouleriana, S. sericea, S. serissima, S. sessilifolia, S. setchelliana, S. silicicola, S. sitchensis, S. sphenophylla, S. stolonifera, S. taxifolia, S. thurberi, S. tracyi, S. triandra, S. turnorii, S. tweedyi, S. tyrrellii, S. uva-ursi, S. vestita, S. viminalis, S. wolfii, S. ×fragilis, S. ×jesupii, S. ×pendulina, S. ×sepulcralis, S. ×smithiana
S. alaxensis, S. alba, S. amygdaloides, S. arbusculoides, S. arctica, S. arctophila, S. argyrocarpa, S. arizonica, S. athabascensis, S. atrocinerea, S. aurita, S. babylonica, S. ballii, S. barclayi, S. barrattiana, S. bebbiana, S. bonplandiana, S. boothii, S. brachycarpa, S. breweri, S. calcicola, S. candida, S. caprea, S. caroliniana, S. cascadensis, S. chamissonis, S. chlorolepis, S. cinerea, S. columbiana, S. commutata, S. cordata, S. daphnoides, S. delnortensis, S. discolor, S. drummondiana, S. eastwoodiae, S. elaeagnos, S. eriocephala, S. euxina, S. exigua, S. famelica, S. farriae, S. floridana, S. fuscescens, S. geyeriana, S. glauca, S. gooddingii, S. hastata, S. herbacea, S. hookeriana, S. humboldtiana, S. humilis, S. interior, S. irrorata, S. jejuna, S. jepsonii, S. lasiandra, S. lasiolepis, S. lemmonii, S. ligulifolia, S. lucida, S. lutea, S. maccalliana, S. melanopsis, S. monochroma, S. monticola, S. myricoides, S. myrsinifolia, S. myrtillifolia, S. nigra, S. niphoclada, S. nivalis, S. nummularia, S. orestera, S. ovalifolia, S. pedicellaris, S. pellita, S. pentandra, S. petiolaris, S. petrophila, S. phlebophylla, S. planifolia, S. polaris, S. prolixa, S. pseudomonticola, S. pseudomyrsinites, S. pulchra, S. purpurea, S. pyrifolia, S. raupii, S. reticulata, S. richardsonii, S. rotundifolia, S. scouleriana, S. sericea, S. serissima, S. sessilifolia, S. setchelliana, S. silicicola, S. sitchensis, S. sphenophylla, S. stolonifera, S. taxifolia, S. thurberi, S. tracyi, S. triandra, S. turnorii, S. tweedyi, S. tyrrellii, S. uva-ursi, S. vestita, S. viminalis, S. wolfii, S. ×fragilis, S. ×jesupii, S. ×pendulina, S. ×sepulcralis, S. ×smithiana
Synonyms S. bonplandiana var. laevigata, S. laevigata var. angustifolia, S. laevigata var. araquipa, S. laevigata var. congesta
Name authority Linnaeus: Sp. Pl. 2: 1021. (1753) Bebb: Amer. Naturalist 8: 202. (1874)
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