Salix hookeriana
Salix pseudomyrsinites
coastal willow, dune willow, Hooker's willow
firmleaf willow, tall blueberry 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 rudimentary or foliaceous on early ones, foliaceous on late ones, (0.6–8 mm), apex acute or obtuse;
petiole shallowly to deeply grooved adaxially, 2.5–8 mm, glabrous or villous adaxially;
largest medial blade (sometimes amphistomatous), narrowly to broadly elliptic, oblong to oblanceolate or obovate, 32–109 × 10–47 mm, 1.8–4.8 times as long as wide, base convex, cuneate, or subcordate, sometimes cordate, margins flat, entire, crenate, or serrulate, apex acute, convex, or acuminate, abaxial surface not glaucous, glabrous or pilose, hairs (white, sometimes also ferruginous), wavy, adaxial slightly glossy, glabrous, pilose, pubescent, moderately densely short-silky, or velvety, midrib remaining pilose or short-hairy, (hairs sometimes also ferruginous, straight and geniculate);
proximal blade margins serrulate or entire;
juvenile blade sometimes reddish or yellowish green, abaxially glabrous, or midrib sparsely pubescent, or densely villous or short-silky, hairs white, sometimes also ferruginous.
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 square, 0.2–0.4–0.6 mm;
filaments distinct, glabrous;
anthers purple turning yellow, 0.4–0.7 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 square or oblong, 0.2–0.4 mm, shorter than stipe;
stipe 0.8–1.4 mm;
ovary pyriform, glabrous, beak slightly bulged below styles;
ovules 11–18 per ovary;
styles 0.4–1.6 mm;
stigmas flat, abaxially non-papillate with rounded tip, or 2 plump lobes, 0.16–0.24–0.32 mm.
5–10 mm.
4.4–6.4 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.
flowering as leaves emerge; staminate stout, 16.5–35.5 × 7–15 mm, flowering branchlet 0.5–12 mm; pistillate moderately or densely flowered, slender or stout, 10.5–68 × 5–20 mm, flowering branchlet 0.5–10 mm;
floral bract brown, black, tawny, or bicolor, 0.6–1.1 mm, apex retuse, abaxially hairy, hairs long-wavy or curly.
= 114.
= 76.
Salix hookeriana
Salix pseudomyrsinites
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 pseudomyrsinites occurs in Nunavut on Akimiski Island in James Bay.
Salix pseudomyrsinites and S. myrtillifolia, although sometimes treated as conspecific (R. D. Dorn 1975), deserve species rank. They differ in chromosome number and are distinct in habit, habitat, and general appearance, including glossiness of leaves, as well as a number of technical characteristics (L. A. Viereck and E. L. Little Jr. 1972; G. W. Argus 1973, 1997). There is no field evidence of hybridization, but some herbarium specimens appear to be intermediates, having the habit or habitat of one species and the leaf hairiness of the other.
Salix myrtillifolia is distinguished from S. pseudomyrsinites by having shrubs low, decumbent, 0.1–0.6 m, rarely to 1 m, of treed bogs and fens, juvenile and mature leaves typically glabrous, stipules usually rudimentary, 0.2–1.8(–5) mm, and styles often shorter, 0.3–0.7 mm; S. pseudomyrsinites has shrubs tall, erect, 1–7 m, of riparian habitats, juvenile leaves pubescent with hairs persisting on mature leaves, at least on adaxial midrib, stipules usually prominent and foliaceous, 0.6–8 mm, and styles often longer, 0.4–1.6 mm.
The nomenclature of these species is confusing. When treating them as varieties E. Hultén (1968) used the name Salix myrtillifolia var. pseudomyrsinites and R. D. Dorn (1975) used the name S. myrtillifolia var. cordata. At the species level, the name S. novae-angliae was used (L. A. Viereck and E. L. Little Jr. 1972; G. W. Argus 1973), but that name is illegitimate (Dorn) and is replaced by S. pseudomyrsinites (Argus 1997).
Hybrids:
Salix pseudomyrsinites forms natural hybrids with S. barrattiana.
Salix pseudomyrsinites × S. barrattiana is a rare hybrid that combines the characters of the two parents.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
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