Salix sect. Glaucae |
Salix subg. Chamaetia |
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Habit | Plants 0.2–6 m, not clonal or clonal by layering. | Shrubs, 0.005–6 m, clonal by layering or rhizomes, rarely root shoots, or not clonal. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stems | erect, trailing, or decumbent; branches flexible at base, usually not glaucous (usually slightly or highly glossy). |
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Buds | usually arctica-type (alba-type in S. athabascensis), scale margins connate. |
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Leaves | stipules usually absent or rudimentary, sometimes foliaceous; petiole shallowly or deeply grooved, convex, or flat adaxially, often not glandular, sometimes with 1 or 2 pairs of spherical glands distally; largest medial blade amphistomatous, hemiamphistomatous, or hypostomatous, (usually pinnately veined), narrowly to broadly elliptic, obovate, subcircular, circular, oblanceolate, narrowly oblong, oblong, or broadly obovate, 0.8–5.5 times as long as wide, angle of base and of apex usually less than or greater than 90o, (abaxial surface usually glaucous), surface hairs usually white, rarely ferruginous; juvenile blade (usually yellowish green), hairs usually white, rarely ferruginous. |
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Staminate flowers | filaments glabrous or hairy. |
abaxial nectary present or absent; stamens 2 (1 in S. uva-ursi); filaments distinct or connate, glabrous or hairy; anthers usually purple, or red turning yellow. |
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Pistillate flowers | abaxial nectary sometimes present, then distinct or connate to adaxial one and forming a cup; ovary pubescent or moderately to very densely villous, tomentose, woolly, or silky, hairs white, cylindrical or flattened. |
abaxial nectary absent or present; ovary usually not glaucous, hairy or glabrous, hairs flattened, ribbonlike, or cylindrical, beak abruptly or gradually tapering to styles or slightly bulged below styles; ovules 4–23 per ovary; styles usually connate; stigmas flat, abaxially non-papillate with rounded tip, or stigmas slenderly or broadly cylindrical, or 2 plump lobes. |
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Largest | medial blades hypostomatous, hemiamphistomatous, or amphistomatous, abaxial surface glaucous (sometimes obscured by hairs). |
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Catkins | from lateral buds. |
flowering as leaves emerge, usually from lateral buds (sometimes subterminal); staminate on flowering branchlet or sessile; pistillate on flowering branchlet, usually stout, globose, or subglobose, sometimes slender; floral bract brown, tawny, or bicolor, apex usually entire, sometimes toothed; pistillate bract usually persistent after flowering. |
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Salix sect. Glaucae |
Salix subg. Chamaetia |
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Distribution | North America; Eurasia |
North America; Eurasia |
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Discussion | Species 8 (3 in the flora). Section Glaucae is placed here in subg. Chamaetia but it clusters with members of subg. Vetrix (G. W. Argus 1997) and could equally well be included there. It includes high polyploids, which probably incorporate genes from members of other sections and subgenera. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Species ca. 133 (27 species in the flora). Eight of the 14 sections recognized in this subgenus are found in the flora area. Subgenus Chamaetia is difficult to separate from subg. Vetrix by morphological characters. It has diverged in habit, which is often dwarfed and rhizomatous; in leaf venation, which often is almost palmate with several veins that diverge from near the base of the blade; in buds, which often contain all the vegetative and reproductive structures that will be produced during the growing season; and less-needed structures such as cataphylls, and in some axillary buds, which are highly reduced. It is possible, as A. K. Skvortsov (1999) pointed out, that this reduction has gone so far that relationships are obscured. The primary characters that distinguish subg. Chamaetia are adaptations to arctic-alpine environments that involve simplification through reduction (Skvortsov). Molecular studies have not resolved any species usually placed in subg. Chamaetia from subg. Vetrix (E. Leskinen and C. Alström-Rapaport 1999; T. Azuma et al. 2000); two unpublished DNA studies also have not revealed a “Chametia” clade. A phenetic study (G. W. Argus 1997) revealed a distinct group separated at a level similar to other subgenera. The exception to this was sect. Glaucae, which sometimes clustered with subg. Chamaetia and other times with subg. Vetrix. This inconsistent clustering may be due to high polyploidy in sect. Glaucae, which may have evolved through hybridization with members of subg. Vetrix, perhaps sect. Hastatae. Although it is clear that subg. Chamaetia is more closely related to subg. Vetrix than to subg. Salix, it is highly probable that it is polyphyletic and does not deserve subgeneric rank. Until more information is available, it is taxonomically useful to treat it as a subgenus. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Source | FNA vol. 7, p. 86. | FNA vol. 7, p. 60. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms | family S. tribe Glaucae | S. section Chamaetia | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | (Fries) Andersson: in A. P. de Candolle and A. L. P. P. de Candolle, Prodr. 16(2): 273. (1868) | (Dumortier) Nasarow: in V. L. Komarov et al., Fl. URSS 5: 31. (1936) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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