Salix hookeriana
Salix gooddingii
coastal willow, dune willow, Hooker's willow
Goodding's black willow, Goodding's willow, Gooding's willow
branches (highly brittle at base), yellow-brown, gray-brown, red-brown, or violet, not or weakly glaucous, glabrous, tomentose, woolly, or sparsely villous to glabrescent (nodes hairy);
branchlets gray-brown, red-brown, or yellow-brown (sometimes color obscured by hairs), glabrous, pilose, moderately densely villous, tomentose, or woolly, scale with inner membranaceous layer free, (not separating from outer layer).
stipules rudimentary or absent on early ones, foliaceous (early deciduous) or rudimentary (sometimes obscured) on late ones, (2.5–7.8–18 mm), apex acuminate, acute, or rounded;
petiole convex to flat, or shallowly grooved adaxially, 4–29 mm, villous, woolly, pilose, or tomentose adaxially;
largest medial blade (sometimes hemiamphistomatous), narrowly to broadly elliptic, oblanceolate, or obovate to broadly obovate, 36–123 × 18–63 mm, 1.5–4.2 times as long as wide, base convex, rounded, subcordate, cordate, or cuneate, margins slightly revolute, crenate, serrate, shallowly serrulate, sinuate, or entire, apex acuminate, acute, or convex, abaxial surface glaucous, pilose, moderately densely tomentose, villous, or woolly, midrib hairy, hairs (white, sometimes also ferruginous), wavy or straight, adaxial highly or slightly glossy, glabrous, pilose, villous, or moderately densely tomentose, midrib and veins hairy (hairs white, sometimes also ferruginous);
proximal blade margins entire or shallowly serrulate;
juvenile blade yellowish, reddish green (sometimes obscured by hairs), pilose or sparsely to densely long-silky, tomentose, woolly, or villous abaxially, hairs white, sometimes also ferruginous, or yellowish.
stipules broad rudiments or foliaceous on early ones, foliaceous on late ones, (glands numerous adaxially), apex rounded to convex;
petiole (sometimes with spherical glands distally), 4–10 mm, pilose adaxially;
largest medial blade (sometimes amphistomatous), narrowly elliptic, very broadly oblong, lorate, or linear, 67–130 × 9.5–16 mm, 4.7–12.4 times as long as wide, base cuneate to convex, margins serrulate to serrate, apex acuminate, caudate, or acute, abaxial surface (usually not glaucous, rarely thinly so), glabrous or puberulent, hairs wavy, adaxial slightly glossy, pilose to glabrescent;
proximal blade margins entire or shallowly serrulate;
juvenile blade sparsely velvety to pilose abaxially, hairs white.
adaxial nectary oblong, ovate, or narrowly oblong, 0.5–1.4 mm;
filaments distinct or slightly basally connate, glabrous or hairy on proximal 1/2 or basally;
anthers yellow, cylindrical or ellipsoid, (0.5–)0.7–1 mm.
abaxial nectary (0.2–)0.3–0.6 mm, adaxial nectary square to ovate, 0.2–0.6 mm, nectaries distinct;
stamens 4–6(–8);
filaments (sometimes basally connate), hairy on proximal 1/2;
anthers 0.4–0.5 mm, (axes straight).
adaxial nectary narrowly oblong, oblong, or square, 0.5–1.4 mm, shorter than stipe;
stipe 0.5–1.8(–2.8) mm;
ovary obclavate or pyriform, glabrous, tomentose, villous, or woolly (hairs wavy), beak sometimes abruptly tapering to styles;
ovules 12–20 per ovary;
styles 0.6–2.3 mm;
stigmas broadly to slenderly cylindrical, 0.3–0.8 mm.
adaxial nectary square (flattened), 0.2–0.6 mm;
stipe 1.2–3.2 mm;
ovary pyriform, (sometimes villous), beak slightly bulged or abruptly tapering to styles;
ovules 12–18 per ovary;
styles 0.1–0.3 mm;
stigmas 0.2–0.29–0.32 mm.
5–10 mm.
6–7 mm.
flowering before or as leaves emerge; staminate slender or stout, 26–73 × 10–27 mm, flowering branchlet 0–10 mm; pistillate densely flowered, slender or stout, 36–92(–140 in fruit) × 10–25 mm, flowering branchlet 0–20 mm;
floral bract brown, black, or bicolor, 1.1–3.6 mm, apex convex, rounded, or acute, abaxially hairy, hairs straight or wavy.
staminate 19–80 × 6–10 mm, flowering branchlet 2–23 mm; pistillate 23–82 × 6–15 mm, flowering branchlet 2–48 mm;
floral bract 1.4–2.4 mm, apex acute or rounded, entire or toothed, abaxially sparsely to moderately densely hairy, hairs wavy; pistillate bract deciduous after flowering.
= 114.
= 38.
Salix hookeriana
Salix gooddingii
Salix hookeriana is primarily a coastal species occurring from northern California northward to Oregon, Washington, and southern Vancouver Island, with disjunct populations on Queen Charlotte Islands, British Columbia, and northward to Yakatut Bay, Turnagain Arm, and Kodiak, Alaska. It was treated by G. W. Argus (1973) and R. D. Dorn (2000) in a broad sense because of an absence of strong distinguishing characters and intergradation in characters that could be used to divide it. It is highly variable and three very similar taxa have been named: S. amplifolia, S. hookeriana (including vars. tomentosa and laurifolia), and S. piperi. Although extremes of these taxa sometimes are recognizable, the intergradation displayed is so great that even attempts to recognize them as varieties are thwarted. The amplifolia variant in Alaska is characterized by having only white leaf hairs, hairy ovaries, no stipules, and catkins often borne on distinct flowering branchlets, but variation can occur within the same population, and typical S. hookeriana on Vancouver Island sometimes displays the same characteristics. The piperi variant, an inland population in western Oregon and Washington, is usually recognized by local botanists as different from coastal populations. It is characterized by leaves and branchlets soon becoming glabrate and stipules prominent. These characteristics, however, sometimes appear in northern California coastal populations, and some inland populations in Oregon include very hairy individuals that are indistinguishable from coastal variants of S. hookeriana. In general, very hairy populations of S. hookeriana are probably an adaptation to marine coastal environments, but some variation may be due to hybridization and introgression with S. scouleriana. Inland populations suggest the influence of S. lasiolepis. Two hexaploid chromosome numbers reported for S. hookeriana from Vancouver Island (R. L. Taylor and S. Taylor 1977) and Queen Charlotte Islands (R. L. Taylor and G. A. Mulligan 1968), British Columbia, indicate that hybridization has played a role in the evolution of this complex. It is possible that each variant of S. hookeriana has had a different, possibly even recurrent, polyploid origin. Further cytological and genetic study is indicated.
The following comparisons may help to distinguish Salix hookeriana, S. lasiolepis, and S. scouleriana.
Vegetative specimens of Salix hookeriana can be distinguished from S. lasiolepis by having floral buds ellipsoid, beaks distinctly long-tapered, densely long-hairy (villous), red-brown, blades usually pilose, villous, or woolly on abaxial surfaces, usually 18–63 mm wide, and 1.5–4.2 times as long as wide; S. lasiolepis has floral buds ovoid, beaks inconspicuous and blunt, sparsely to moderately densely short-hairy (velvety), yellowish to red-brown, blades usually tomentose on abaxial surfaces, usually 6–32 mm wide, and 3.2–9.6 times as long as wide.
Salix hookeriana is distinguished from S. scouleriana by having branchlets with spreading hairs (woolly or tomentose to glabrate), petioles usually pilose to tomentose, blades typically narrowly elliptic but variable, stigmas 0.3–0.74, short in relation to styles (0.6–2.3 mm), and pistillate nectaries 0.5–1.4 mm, shorter or longer than stipes; S. scouleriana has branchlets usually with short, erect hairs (velutinous), sometimes spreading (villous or tomentose), petioles velvety or villous adaxially, blades typically oblanceolate but variable, stigmas 0.4–1.04 mm, long in relation to styles (0.2–0.6 mm), and pistillate nectaries 0.2–0.8 mm, shorter than stipes.
Hybrids:
Salix hookeriana forms natural hybrids with S. barclayi and S. scouleriana. Variation in some S. hookeriana populations suggests hybridization with S. lasiolepis but no positive identifications have been made. R. D. Dorn (2000) doubted that hybridization in California between these species with different chromosome numbers was possible, but species with different chromosome numbers do hybridize [for example, S. athabascensis (4x) × S. pedicellaris (2x)]; synthetic hybridization studies are indicated.
Salix hookeriana × S. scouleriana: Plants from southern British Columbia with leaves similar to S. hookeriana but with prominent stipules, catkins both erect and recurving, and relatively long stigmas were thought by J. K. Henry (1915) to be this hybrid.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
Salix gooddingii and S. nigra are closely related and are sometimes treated as conspecific (C. R. Ball 1950). Salix gooddingii has yellow-brown or pale gray-brown branches, capsules 6–7 mm, and ovaries usually glabrous but pilose in ca. 20% of specimens. Salix nigra has red-brown to dark gray-brown branches, capsules 3–5 mm, and ovaries almost always glabrous. A single plant with pilose ovaries was found in Ontario, Canada; reports (W. A. Archer 1965) of S. nigra with hairy ovaries in Alabama, Arkansas, Illinois, Iowa, Kansas, Massachusetts, Oklahoma, and Texas could not be confirmed. Ranges of these taxa overlap in west-central Texas, where there is evidence of intergradation; they rarely occur in the same population. The map by E. L. Little Jr. (1971), who treated them as conspecific, shows a significant range disjunction between the two.
Catkins of Salix gooddingii flowering in March and early April are sometimes borne in leaf axils. This suggests that the sylleptic condition, typical of S. bonplandiana, is sometimes ecotypic.
Hybrids:
Salix gooddingii forms natural hybrids with S. amygdaloides and S. nigra. Hybrids with S. lasiandra have been reported (C. K. Schneider 1921); no convincing specimens have been seen.
Salix gooddingii × S. laevigata: In Arizona, a population of young plants displays intermediate characteristics. They have leaf blades sparsely glaucous abaxially, as in S. laevigata, but narrow, often amphistomatous, and with petioles sometimes not glandular distally, as in S. gooddingii. Both parental species occur in the region. This hybrid was also reported by C. K. Schneider (1921) from California.
Salix gooddingii × S. nigra: This hybrid may occur in western Texas where the parental species overlap. Some specimens from that area seem to be “intermediate” in branch color, but the differences are subtle.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
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