Salix subg. Protitea |
Salix laevigata |
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polished willow, red willow |
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Habit | Shrubs or trees, 1–30 m, not clonal, or clonal by stem fragmentation. | Trees, 2–15 m. Stems: branches flexible to highly brittle at base, gray-brown to yellow-brown, glabrous or villous; branchlets yellow-brown or red-brown, glabrous, densely villous, velvety, or pilose, nodes hairy. | ||||||||||||||||||||||||||||
Stems | usually erect; branches flexible to highly brittle at base or throughout, glaucous or not. |
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Buds | alba-type, scale margins distinct, overlapping. |
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Leaves | stipules on early ones usually rudimentary, sometimes absent or foliaceous, on late leaves foliaceous, rarely rudimentary (deciduous early or autumn); petiole usually deeply grooved adaxially (except S. floridana), not usually glandular distally (sometimes with basilaminar, spherical, or foliaceous glands); largest medial blade usually hypostomatous, sometimes amphistomatous, narrowly oblong, oblong, narrowly ovate, lorate, lanceolate, narrowly elliptic, or linear, 2.5–13 times as long as wide, angles of base and apex less than 90o, surface hairs usually white, sometimes also ferruginous; juvenile blade hairs white, sometimes also ferruginous. |
stipules rudimentary grading into foliaceous or absent on early ones, usually foliaceous on late ones, apex acute, acuminate, rounded or convex; petiole (shallowly or deeply grooved adaxially, margins sometimes touching, sometimes with basilaminar glands, thickening), 3.5–18 mm, pubescent to glabrescent adaxially; largest medial blade lorate, narrowly oblong, narrowly elliptic, lanceolate, or obovate, 53–190 × 11–35 mm, 2.8–9 times as long as wide, base convex, subcordate, rounded, or cuneate, margins crenate, entire, or finely serrulate, apex acuminate, acute, or caudate, abaxial surface glabrous or pubescent, hairs spreading, white and/or ferruginous, adaxial highly or slightly glossy, glabrous or pubescent, midrib sometimes villous; proximal blade margins entire; juvenile blade glabrous or moderately densely long-silky to pilose abaxially, hairs white and/or ferruginous. |
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Staminate flowers | abaxial nectary present; stamens 3–7[–9]; filaments usually distinct, sometimes connate less than 1/2 their lengths, usually hairy basally, sometimes on proximal 1/2; anthers yellow, usually globose. |
abaxial nectary 0.4–0.6 mm, adaxial nectary oblong, square, or ovate, 0.3–0.6 mm, nectaries distinct; stamens 3–7; filaments (sometimes basally connate), hairy on proximal 1/2 or basally; anthers 0.4–0.6 mm. |
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Pistillate flowers | abaxial nectary absent, (adaxial nectary shorter than stipe); ovary not glaucous, usually glabrous, sometimes villous, beak slightly bulged below or tapering to styles; ovules 4–24 per ovary; styles usually connate, sometimes distinct distally; stigmas usually flat, abaxially non-papillate, tip usually rounded, or stigmas slenderly cylindrical, or 2 plump lobes. |
adaxial nectary square, 0.2–0.6 mm; stipe 1.4–2.8 mm; ovary pyriform, obturbinate, or ellipsoidal, beak slightly bulged below styles; ovules 12–24 per ovary; styles 0.1–0.2 mm; stigmas 0.2–0.23–0.28 mm. |
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Capsules | 3–5.5 mm. |
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Catkins | usually flowering as leaves emerge (sometimes throughout season, axillary, sessile in S. bonplandiana), from lateral buds; staminate from flowering branchlet, slender to stout; pistillate from flowering branchlet, usually loosely flowered, slender to stout; floral bract usually tawny, sometimes greenish, apex entire, erose, 2-fid, or irregularly toothed; pistillate bract deciduous (persistent in S. floridana, sometimes S. bonplandiana) after flowering. |
staminate 31–83 × 7–13 mm, flowering branchlet 2–26 mm; pistillate 28–79 × 6–11 mm, flowering branchlet 3–14 mm; floral bract 1.6–3.4 mm, apex rounded or acute, irregularly toothed or entire, abaxially sparsely to moderately densely hairy proximally or throughout, hairs wavy; pistillate bract deciduous after flowering. |
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Salix subg. Protitea |
Salix laevigata |
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Phenology | Flowering (Dec-)Feb or mid Apr-early Jun. | |||||||||||||||||||||||||||||
Habitat | Riparian forests along streams, seepage areas, springs, subalkaline or brackish lakeshores, canyons, ditches | |||||||||||||||||||||||||||||
Elevation | 0-2200 m (0-7200 ft) | |||||||||||||||||||||||||||||
Distribution | North America; Mexico; Central America; West Indies; Asia |
AZ; CA; NV; OR; UT; Mexico (Baja California, Baja California Sur)
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Discussion | Species 33 (7 species in the flora). Two of the three sections recognized in this subgenus are found in the flora area. Subgenus Protitea includes the New World members of sects. Floridanae and Humboldtianae. These sections often are placed in subg. Salix along with sect. Salicaster (R. D. Dorn 1976; G. W. Argus 1997; A. K. Skvortsov 1999); including them in a separate subgenus better emphasizes their position within the genus. Taxa in subg. Protitea are characterized by bud-scales with distinct, overlapping adaxial margins, flowers with 3–7[–9] stamens, and, usually, a tropical distribution. When subg. Protitea was described, it did not receive strong support. The debate was whether the multistaminate willows should be grouped on stamen number (T. Nakai 1928) or bud-scale characteristics (A. Kimura 1928). In a cladistic study of multistaminate Salix (Zhang M. L. 1994), members of subg. Protitea were in a clade that included two members of sect. Salicaster (subg. Salix). In a phenetic study of New World Salix (Argus), subg. Protitea appeared as a separate branch but was closely associated with a branch including members of subg. Salix. Two molecular studies provided equivocal results. A study based on ribosomal DNA (E. Leskinen and C. Alström-Rapaport 1999) included only one species from subg. Protitea (S. amygdaloides); it grouped with S. alba (subg. Salix). A study based on cpDNA, rbcL gene sequence (T. Azuma et al. 2000) placed members of subg. Protitea in a clade along with taxa from subg. Salix and subg. Longifoliae. Within this clade, species included here in subg. Protitea appeared on different branches. These results argue against the recognition of subg. Protitea but they were not definitive because the molecular cladistic studies included too few species of the subgenus and the morphological phenetic study did not account for polyploidy. All members of subg. Protitea for which we have counts are diploid; species in sect. Salicaster, the other section with multistaminate species, are polyploid. It is likely that sect. Salicaster, which is placed here in subg. Salix, originated through hybridization between members of subg. Protitea and subg. Salix followed by polyploidy. This would account for the occurrence of both multiple stamens and calyptrate bud-scales in the polyploid members of subg. Salix. Placing the diploid, multistaminate Salix with distinct, overlapping bud-scales in a subgenus separate from the polyploid, multistaminate Salix (sect. Salicaster) with calyptrate bud-scales would make subg. Protitea a more natural group. A study including a large sample of the 33 species in this subgenus would help resolve this question. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Hybrids: Salix laevigata forms natural hybrids with S. gooddingii. Related Species: Salix humboldtiana Willdenow: Humboldt willow is not known to occur in the flora area. It is characterized by: trees, 4–25 m; branches highly brittle at base, bud-scale margins distinct and overlapping adaxially; stipules on late leaves rudimentary or foliaceous; largest medial leaf blade usually linear, abaxial surface not glaucous, adaxial dull; pistillate bract deciduous after flowering; stamens 3–7; capsules with distinct, often raised, white veins. It occurs throughout much of Mexico to central Chile. Salix humboldtiana is closely related to S. nigra in its generally narrow leaf blades, which are not glaucous abaxially. The two differ in the following characters: S. humboldtiana has leaf blades linear to sometimes narrowly oblong (10–28.6 times as long as wide), ovaries usually ovoid to ellipsoid, ovary walls often stomatiferous and with raised, white veins, and capsule valves relatively thick, slightly recurved. S. nigra has leaf blades usually narrowly lanceolate (6–13 times as long as wide), ovaries pyriform to obclavate, ovary walls neither stomatiferous nor notably veined, and capsule valves relatively thin and strongly recurved. Both species occur in Chihuahua, Mexico. The report by R. I. Lonard et al. (1991) that specimens identified as Salix nigra from the lower Rio Grande, Texas, resemble S. humboldtiana in having strongly veined capsules suggests that S. humboldtiana, or intergrades with that species, may occur in Texas. Attempts to locate a voucher specimen were unsuccessful; because strongly veined capsules are diagnostic, further field study is indicated. An earlier name, Salix chilensis Molina, has been applied to this species; it does not seem to pertain to this taxon (C. K. Schneider 1918). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 7, p. 30. | FNA vol. 7, p. 34. | ||||||||||||||||||||||||||||
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Synonyms | S. bonplandiana var. laevigata, S. laevigata var. angustifolia, S. laevigata var. araquipa, S. laevigata var. congesta | |||||||||||||||||||||||||||||
Name authority | Kimura: Bot. Mag. (Tokyo) 42: 290. (1928) | Bebb: Amer. Naturalist 8: 202. (1874) | ||||||||||||||||||||||||||||
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