Salix brachycarpa |
Salix amygdaloides |
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barren-ground willow, short-fruit willow, small-fruit willow |
peach-leaf willow |
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Habit | Plants 0.2–1.5 m, not clonal. | Trees, 4–20 m. Stems: branches flexible to ± brittle at base, yellow to gray-brown, glabrous; branchlets yellow-brown, gray-brown, or red-brown, glabrous. | ||||
Stems | erect or decumbent; branches gray-brown or red-brown, villous or short-silky to glabrescent; branchlets red-brown, long-silky, villous, or woolly. |
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Leaves | stipules absent or rudimentary on early ones, foliaceous or rudimentary on late ones; petiole (deeply to shallowly grooved adaxially), (0.5–)1–3(–4) mm, (usually shorter than or barely exceeding subtended bud); largest medial blade hypostomatous, narrowly oblong, oblong, narrowly elliptic, elliptic, narrowly oblanceolate, ovate, or obovate, base rounded, convex, cordate, or subcordate, margins flat, entire, apex rounded, acute, or convex, abaxial surface (sometimes obscured by hairs), densely villous, woolly, or long-silky, adaxial slightly glossy, pilose, villous, or long-silky to glabrescent, (hairs straight or wavy); proximal blade margins entire; juvenile blade very densely long-silky abaxially. |
stipules absent or rudimentary on early ones, foliaceous or rudimentary on late ones, apex rounded; petiole (margins covering groove, not glandular or with spherical glands distally), 7–21 mm, glabrous or puberulent adaxially; largest medial blade (sometimes amphistomatous), very narrowly elliptic, elliptic, lanceolate, or lorate, 55–130 × 24–37 mm, 2.8–6 times as long as wide, base convex, cuneate, or cordate, margins serrulate, apex acuminate to caudate, abaxial surface glaucous, glabrous, adaxial dull, glabrous or sparsely pubescent along midrib; proximal blade margins entire or shallowly serrulate; juvenile blade glabrous or pubescent abaxially, hairs white and/or ferruginous. |
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Staminate flowers | abaxial nectary (0–)0.5–1.5 mm, adaxial nectary 0.5–1.4 mm, nectaries distinct or connate and cup-shaped; filaments distinct or connate less than 1/2 their lengths, glabrous or hairy throughout or on proximal 1/2; anthers ellipsoid, shortly cylindrical, or globose, 0.3–0.8 mm. |
abaxial nectary 0.2–0.7 mm, adaxial nectary narrowly oblong to square, 0.3–0.8 mm, nectaries distinct; stamens 3–7; filaments hairy on proximal 1/2 or basally; anthers 0.5–0.6 mm. |
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Pistillate flowers | abaxial nectary often present, adaxial nectary longer than stipe; stipe 0–0.6 mm; ovary pyriform, very densely villous, tomentose, or woolly, beak slightly bulged below styles; ovules 2–10 per ovary; styles connate to distinct 1/2 their lengths, 0.4–1.5 mm; stigmas broadly or slenderly cylindrical, 0.24–0.3–0.48 mm. |
adaxial nectary square, 0.1–0.6 mm; stipe 1.4–3.2 mm; ovary pyriform, beak slightly bulged below styles; ovules 16–18 per ovary; styles 0.2–0.4 mm; stigmas 0.24–0.31–0.4 mm. |
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Capsules | 3–6.5 mm. |
3–7 mm. |
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Catkins | staminate 5.3–24 × 4–10 mm, flowering branchlet 0.3–24(–43) mm; pistillate (and staminate) densely flowered, globose, subglobose, or stout, 6–25 × 4–15 mm, flowering branchlet 0.3–11 mm; floral bract tawny or greenish, 1–3 mm, apex rounded or convex, entire, abaxially hairy, hairs straight or wavy. |
staminate 23–80 × 5–12 mm, flowering branchlet 3–28 mm; pistillate 41–110(–127 in fruit) × 8–16 mm, flowering branchlet 17–35 mm; floral bract 1.5–2.8 mm, apex acute to rounded, entire or toothed, abaxially sparsely to moderately densely hairy proximally, hairs wavy; pistillate bract deciduous after flowering. |
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2n | = 38. |
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Salix brachycarpa |
Salix amygdaloides |
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Phenology | Flowering early Apr–Jun. | |||||
Habitat | Moist to mesic floodplains, shores of lakes on sandy, silty, or gravelly substrates, marshes, wet sand dune slacks | |||||
Elevation | 60-2400 m (200-7900 ft) | |||||
Distribution |
CA; CO; ID; MT; NM; OR; UT; WA; WY; AB; BC; MB; NT; NU; ON; QC; SK; YT
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AZ; CO; IA; ID; IL; IN; KS; KY; MI; MN; MO; MT; ND; NE; NM; NV; NY; OH; OK; OR; PA; SD; TX; UT; WA; WI; WY; AB; BC; MB; ON; QC; SK
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Discussion | Varieties 2 (2 in the flora). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Presence of Salix amygdaloides in Massachusetts, New Hampshire, and Vermont has not been verified; its occurrence in those New England states was reported by H. A. Gleason and A. Cronquist (1991), and by M. L. Fernald (1950). Hybrids: Salix amygdaloides forms natural hybrids with S. gooddingii and S. nigra. Hybrids with S. caroliniana (N. M. Glatfelter 1898) and S. eriocephala (M. L. Fernald 1950) have been reported; no convincing specimens have been seen. Controlled pollination between S. amygdaloides and S. eriocephala, S. interior, and S. petiolaris set no seed; controlled pollination with S. lucida produced a few seeds; some seedlings suffered necrosis in the cotyledon stage (A. Mosseler 1990). Salix amygdaloides × S. gooddingii (S. ×wrightii Andersson): This hybrid occurs throughout the Rio Grande Valley, Texas, and New Mexico (C. K. Schneider 1919; C. R. Ball 1961), and at Happy and Rio Frio, Texas, and Virgil Run, Arizona. The leaves are somewhat glaucous abaxially, as in S. amygdaloides, but they are linear to narrowly elliptic and branchlets are sparsely pubescent as in S. gooddingii. Salix amygdaloides × S. nigra (S. ×glatfelteri C. K. Schneider) resembles S. amygdaloides in leaves somewhat glaucous abaxially, but usually linear or narrowly elliptic, as in S. nigra. The stipules are not as prominent as in S. nigra but are foliaceous on late leaves; it should be expected wherever the ranges of the two species overlap. The hybrid is common in Missouri, where N. M. Glatfelter (1894) estimated that ca. 40% of the populations were hybrids, and in Illinois (R. H. Mohlenbrock 1980; G. Wilhelm, pers. comm.). Putative hybrids occur also in Ontario. Narrow leaves are typical of juvenile plants of S. amygdaloides but even at that stage they tend to be broadest at the midpoint or toward the base rather than in a midzone as in S. nigra. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 7, p. 86. | FNA vol. 7, p. 37. | ||||
Parent taxa | ||||||
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Name authority | Nuttall: N. Amer. Sylv. 1: 69. (1842) | Andersson: Öfvers. Kongl. Vetensk.-Akad. Förh. 15: 114. (1858) | ||||
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