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mountain willow, Scouler willow, Scouler's willow

blanket-leaf willow

Habit Shrubs or trees, 1–10(–20) m. Stems: branches gray-brown, yellow-brown, or red-brown, not glaucous, glabrous or tomentose; branchlets yellow-green or yellow-brown, sparsely to densely villous, tomentose, or velvety. Shrubs, 1–3 m, (forming clones by layering).
Stems

branches yellow-brown, gray-brown, or red-brown, not glaucous, villous in patches to glabrescent;

branchlets gray-brown or red-brown, very densely villous.

Leaves

stipules absent, rudimentary, or foliaceous on early ones, foliaceous on late ones, (1–16 mm), apex acute or acuminate;

petiole convex to flat adaxially, 2–13 mm, velvety or villous adaxially;

largest medial blade usually oblanceolate, sometimes narrowly elliptic, elliptic or obovate, 29–100 × 9–37 mm, 1.7–3.9 times as long as wide, base cuneate or convex, margins strongly to slightly revolute or flat, entire, remotely serrate, crenate, or sinuate, (glands submarginal or epilaminal), apex acuminate, convex, or rounded, abaxial surface glaucous, sparsely to densely short- to long-silky or woolly, hairs (white, sometimes also ferruginous), wavy or straight, adaxial slightly glossy, pilose or moderately densely short-silky, midrib velutinous or villous, (hairs white, sometimes also ferruginous);

proximal blade margins entire, serrulate, or crenulate;

juvenile blade reddish or yellowish green, sparsely to densely villous, short- or long-silky abaxially, hairs white, sometimes also ferruginous.

stipules foliaceous, apex acute to acuminate;

petiole convex to flat adaxially, 5–12 mm, villous or tomentose adaxially, (strongly ventricose around floral buds);

largest medial blade (apparently hypostomatous but surfaces obscured by hairs), narrowly oblong, narrowly elliptic, elliptic, or obovate, 36–84 × 19–40 mm, 1.8–3.6 times as long as wide, base convex or cuneate, margins slightly revolute, entire, apex convex or acuminate, abaxial surface very densely woolly-tomentose, hairs wavy, adaxial dull, moderately to very densely, villous-tomentose;

proximal blade margins entire;

juvenile blade color obscured by hairs, very densely tomentose-woolly abaxially, hairs white.

Staminate flowers

adaxial nectary oblong or square, 0.4–0.9 mm;

filaments distinct, glabrous or hairy on proximal 1/2;

anthers purple turning yellow, ellipsoid to shortly cylindrical, 0.7–1.2 mm.

adaxial nectary oblong to narrowly oblong, 0.6–1.5 mm;

filaments distinct;

anthers yellow, ellipsoid, 0.6–0.7 mm.

Pistillate flowers

adaxial nectary oblong or square, 0.2–0.8 mm, shorter than stipe;

stipe 0.8–2.3 mm;

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

ovules 10–18 per ovary;

styles 0.2–0.6 mm;

stigmas slenderly cylindrical, 0.4–0.82–1.04 mm.

adaxial nectary oblong or obtriangular, 0.5–1.1 mm;

stipe 0–0.3 mm;

ovary pyriform, beak gradually tapering to styles;

ovules 12–14 per ovary;

styles 1.2–2.2 mm;

stigmas 0.52–0.75–1 mm.

Capsules

4.5–11 mm.

4–7 mm.

Catkins

flowering before leaves emerge; staminate stout or subglobose, 18–40.5 × 8–22 mm, flowering branchlet 0–4 mm; pistillate very densely flowered, slender or stout, 18–60(–90 in fruit) × 10–22 mm, flowering branchlet 0–8 mm;

floral bract brown, black, or bicolor, 1.5–4.5 mm, apex rounded or acute, abaxially hairy, hairs straight.

flowering before leaves emerge; staminate stout, 40–56 × 14–15 mm, flowering branchlet 0 mm; pistillate densely flowered, slender, 35–125(–130 in fruit) mm, flowering branchlet 0 mm;

floral bract brown or black, 2–3 mm, apex convex to rounded, abaxially hairy, hairs straight.

2n

= 76.

= 38.

Salix scouleriana

Salix silicicola

Phenology Flowering late Feb-mid Jun. No data are available on flowering time in the wild; in cultivation flowering is early May.
Habitat Dry conifer forests, mature woods on edges of streams and lakes, treed bogs, meadows, subalpine slopes, springs, pine barrens, openings in old burns, arroyos and disturbed sites, sandy, silty-clay, or gravelly, igneous substrates Active sand dunes
Elevation 0-3500 m (0-11500 ft) 20-500 m (100-1600 ft)
Distribution
from FNA
AK; AZ; CA; CO; ID; MT; NM; NV; OR; SD; UT; WA; WY; AB; BC; MB; NT; SK; YT; Mexico (Chihuahua, Sonora)
[WildflowerSearch map]
[BONAP county map]
from FNA
NU; SK
[BONAP county map]
Discussion

Western Salix scouleriana and eastern S. humilis are closely related and are sometimes difficult to separate. Although there is an apparent range disjunction between them in western Manitoba, it may be a collecting gap. In general, S. scouleriana differs from S. humilis in being a taller shrub, sometimes even tree-like, with broader leaves and longer catkins, floral bracts, stigmas, and styles, but these quantitative characteristics all overlap. The apparent difference in anther length (S. scouleriana 0.7–1.2 mm; S. humilis 0.4–0.6 mm) may be correlated with a difference in chromosome number. Salix scouleriana is tetraploid (Y. Suda and G. W. Argus 1968); S. humilis has been reported to be both diploid (Suda and Argus; L. Zsuffa and Y. Raj, unpubl.) and tetraploid (R. D. Dorn 1976). The latter count was from the same population as the one by Suda and Argus. Further chromosome counts are indicated.

See 77. Salix hookeriana for comparative descriptions.

Hybrids:

Salix scouleriana forms natural hybrids with S. hookeriana, S. planifolia, and S. pulchra.

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

Comparisons of genetic variation in Salix alaxensis var. alaxensis from British Columbia and S. silicicola from Lake Athabasca sand dunes, Saskatchewan, based on isozyme loci, fit predicted relationships between progenitor and derived taxon (B. G. Purdy and R. J. Bayer 1995). Allelic diversity of S. silicicola was a subset of that of S. alaxensis, there was less genetic variation in S. silicicola than in S. alaxensis, and interspecific genetic variation within the two species was similar and relatively very high. This suggested a recent origin for the derived S. silicicola.

Salix silicicola is a uniform population that differs from S. alaxensis in its very densely villous or tomentose leaves and branchlets. These characters seem to be an adaptation to reduce sand abrasion and water loss in a sand dune environment. It is unlikely that it would have evolved in situ but probably derived from a pre-adapted source such as the one represented by specimens of putative S. silicicola from Pelly Lake, Nunavut. The isozyme study did not include specimens from that population or of S. alaxensis from Northwest Territories from which S. silicicola is likely to have been derived. Occurrence of S. silicicola-like plants in northern continental Nunavut suggests that during the late Pleistocene, it had a wider range, which now is represented by two disjunct populations. The question of appropriate taxonomic rank for the derived taxon is still unresolved. Although S. silicicola is different from S. alaxensis in its general appearance, they are very similar genetically, and argument could be made for treating them as varieties (B. Boivin 1966b).

Hybrids:

Salix silicicola forms natural hybrids with S. brachycarpa var. psammophila.

of conservation concern

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

Source FNA vol. 7, p. 131. FNA vol. 7, p. 147.
Parent taxa Salicaceae > Salix > subg. Vetrix > sect. Cinerella Salicaceae > Salix > subg. Vetrix > sect. Villosae
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. 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. 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. 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. 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. 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. scouleriana var. poikila S. alaxensis var. silicicola
Name authority Barratt ex Hooker: Fl. Bor.-Amer. 2: 145. (1838) Raup: J. Arnold Arbor. 17: 236, plate 194. (1936)
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