Salix lucida
Salix cinerea
Pacific willow (var. lasiandra), shining willow, whiplash willow (ssp. caudata)
gray willow, large gray or gray willow, large gray willow
stipules foliaceous, apex convex to rounded;
petiole shallowly to deeply grooved adaxially, 5–13 mm, with clusters of spherical or foliaceous glands distally, glabrous, pilose, or densely villous adaxially;
largest medial blade usually hypostomatous or hemiamphistomatous, rarely amphistomatous, lorate, very narrowly elliptic, narrowly elliptic, or lanceolate, (24–)55–133 × 11–43 mm, 2.5–6.2 times as long as wide, base convex or cuneate, margins flat, serrulate, apex acuminate to caudate, abaxial surface usually not glaucous (rarely so), glabrous, pilose, or moderately densely villous or long-silky, hairs appressed or spreading, white and/or ferruginous, straight or wavy, (coarse, caducous), adaxial (secondary veins flat or protruding), slightly or highly glossy, glabrous, pilose, or long-silky, hairs white and/or ferruginous;
proximal blade margins entire and glandular-dotted, or serrulate or crenulate;
juvenile blade reddish or yellowish green, glabrous or densely villous or long-silky abaxially, hairs white and ferruginous.
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.
abaxial nectary 0.5–1.1 mm, adaxial nectary square or ovate, 0.3–0.9 mm, nectaries connate and cup-shaped;
stamens 3–6;
filaments distinct, hairy on proximal 1/2 or basally;
anthers ellipsoid, shortly cylindrical, obovoid, or globose, 0.6–0.8 mm.
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.
adaxial nectary square or ovate, (swollen), 0.2–0.5 mm, shorter than stipe;
stipe 0.5–2 mm;
ovary pyriform, beak slightly bulged below or gradually tapering to styles;
ovules 18–24 per ovary;
styles connate or distinct 1/2 their lengths, 0.5–0.8 mm;
stigmas flat, abaxially non-papillate with rounded tip, broadly cylindrical, or 2 plump lobes, 0.24–0.31–0.42 mm.
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.
5–7 mm.
5–5.6 mm.
staminate 19–69 × 4–14 mm, flowering branchlet 5–23 mm; pistillate (fruiting in summer), moderately densely to loosely flowered, slender to stout, 23–56(–70 in fruit) × 8–12 mm, flowering branchlet 8–25 mm;
floral bract 1.5–3 mm, apex convex or rounded, entire or toothed, abaxially sparsely hairy throughout or proximally, hairs wavy.
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.
= 76.
= 76.
Salix lucida
Salix cinerea
The Virginia plants of Salix lucida are introduced (G. W. Argus 1986).
The Salix lucida complex is a group of three weakly delimited taxa, S. lasiandra var. caudata, S. lasiandra var. lasiandra, and S. lucida. The morphological characters used to separate them (leaves amphistomatous or hypostomatous and blades glaucous abaxially or not) are usually geographically correlated, but there are exceptions. G. W. Argus (1986b) proposed, based on principal components analysis of morphological data, to treat them as a single species consisting of three subspecies. The geographic overlap of the northeastern S. lucida and the western S. lasiandra is a relatively small area in central Saskatchewan. Evidence of intergradation was based on cultivation of a plant that, in the wild, had leaves that were not glaucous abaxially but were glaucous in cultivation. It seems best to treat them as two species, S. lucida and S. lasiandra, the latter with two varieties, var. lasiandra and var. caudata.
Hybrids:
Salix lucida forms natural hybrids with S. alba and S. nigra. Hybrids with S. serissima have been reported (M. L. Fernald 1950) but no convincing specimens have been seen. Attempts to hybridize S. lucida with members of subg. Protitea (S. amygdaloides), subg. Longifoliae (S. interior), and subg. Vetrix (S. discolor, S. eriocephala, and S. petiolaris) were unsuccessful (A. Mosseler 1990).
Salix lucida × S. nigra (S. ×schneideri B. Boivin) seems to be a rare intersubgeneric hybrid between tetraploid S. lucida and diploid S. nigra. It is known only from the type specimen, an infertile plant, growing with both parents. It resembles S. lucida in bud-scale margins connate, in petiolar glands stalked or foliaceous, and in leaf shape, and S. nigra in stipules rudimentary on proximal leaves and sometimes even on early leaves, stipule apex acute, pistillate catkins relatively long and slender, and styles relatively short.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
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.)
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