Salix hookeriana
Salix bebbiana
coastal willow, dune willow, Hooker's willow
beak willow, Bebb willow, Bebb's willow, gray or Bebb's or long-beak willow, gray willow, grey willow, long-beak 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).
branches divaricate, sometimes ± brittle at base, yellow-brown to dark red-brown, not or weakly glaucous, pilose to glabrescent, peeled wood often with very dense striae, to 25 mm;
branchlets yellow-green or red-brown, moderately to very densely villous to glabrescent.
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 rudimentary or absent on early ones, apex acute, acuminate, or convex;
petiole convex to flat adaxially, 2–5.5–13 mm, pubescent adaxially;
largest medial blade narrowly oblong, narrowly elliptic, elliptic, oblanceolate, or obovate, 20–44–87 × 10–16–45 mm, base cuneate, convex, or rounded, margins flat, entire, crenate, or irregularly serrate, glands submarginal, apex acute, acuminate, or convex, abaxial surface glaucous, moderately densely pubescent or long-silky to glabrescent, hairs white or gray, wavy, adaxial finely impressed-reticulate, dull or slightly glossy, moderately densely pubescent, sparsely short-silky, or glabrescent, hairs white or gray;
proximal blade margins entire, gland-dotted;
juvenile blade yellowish green or reddish, pilose or sparsely to moderately densely tomentose or long-silky 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.
adaxial nectary oblong or ovate, 0.3–0.8 mm;
filaments distinct or connate less than 1/2 their lengths, glabrous or hairy on proximal 1/2;
anthers yellow or purple turning yellow, ellipsoid or shortly cylindrical, 0.5–0.8 mm.
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 oblong or square, 0.3–0.8 mm;
ovary obclavate, beak slightly bulged below styles (long-beaked);
ovules 6–16 per ovary;
styles 0.1–0.4 mm;
stigmas slenderly to broadly cylindrical.
5–10 mm.
5–9 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 flowering just before leaves emerge, pistillate flowering as leaves emerge; staminate stout to globose, 10–42 × 7–16 mm, flowering branchlet 0.5–11 mm; pistillate loosely flowered, stout, slender, or subglobose, 16.5–85 × 9–32 mm, flowering branchlet 1–26 mm;
floral bract tawny, 1.2–3.2 mm, apex rounded, abaxially hairy to glabrescent, hairs straight or wavy.
= 114.
= 38.
Salix hookeriana
Salix bebbiana
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 bebbiana occurs in Nunavut on Akimiski Island in James Bay.
Hybrids:
Salix bebbiana forms natural hybrids with S. candida, S. geyeriana, S. humilis, and S. petiolaris. Reports of hybrids with S. discolor (C. K. Schneider 1921; M. L. Fernald 1950) are not based on convincing specimens, and synthetic hybrids could not be made (G. W. Argus 1974). Reports of hybrids with S. eriocephala and S. myricoides (Fernald) are unverified. Controlled pollinations with S. eriocephala and S. interior had low seed viability (A. Mosseler 1990).
Salix bebbiana × S. candida (S. ×cryptodonta Fernald, as species) is intermediate between parental species. It resembles S. candida in having juvenile leaves densely woolly, mature leaves sparsely to moderately woolly abaxially, margins strongly revolute to crenulate, and ovaries woolly; and S. bebbiana in having stipes 2.8–3 mm and capsules long-beaked, 8–9 mm. The hybrid commonly occurs in Newfoundland.
Salix bebbiana × S. geyeriana: A plant with the pistillate catkins and flowers of S. bebbiana and the narrow, entire or slightly serrulate leaves with white and ferruginous hairs of S. geyeriana was collected by R. D. Dorn in a mixed population in Montana (Beaverhead County).
Salix bebbiana × S. humilis: Reported by C. K. Schneider (1921) and M. L. Fernald (1950) and successfully synthesized by G. W. Argus (1974, 1986).
Salix bebbiana × S. petiolaris is known from Ontario, based on an infertile pistillate specimen, and from Alberta and Saskatchewan, where it is relatively uncommon. It was successfully synthesized (G. W. Argus 1974, 1986) and controlled pollinations showed high seed viability (A. Mosseler 1990).
(Discussion copyrighted by Flora of North America; reprinted with permission.)
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