Salix exigua var. hindsiana |
Salicaceae |
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Hind' narrowleaf willow, Hind' willow, Hinds' willow, sandbar willow |
willow family |
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Habit | Shrubs or trees, 1–5(–17) m. Stems: branches gray-brown or red-brown, glabrous or hairy; branchlets yellow-brown or red-brown, pubescent or densely long-silky-villous, hairs spreading, appressed. | Shrubs or trees, heterophyllous or not, sometimes clonal, forming clones by root shoots, rhizomes, layering, or stem fragmentation; glabrous or glabrescent to pubescent; branching monopodial or sympodial. | ||||||||||||
Stems | erect to pendent; branched. |
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Leaves | stipules rudimentary on early ones, foliaceous or rudimentary on late ones; petiole puberulent, villous, or short-silky adaxially; largest medial blade (sometimes hypostomatous) linear, 39–96 × 5.3–14 mm, 6.5–31 times as long as wide, abaxial surface glabrous or densely silky-villous to glabrescent, hairs appressed or spreading, straight, adaxial sparsely to very densely long-silky-villous; juvenile blade densely silky-villous abaxially (hairs relatively long, spreading, appressed). |
persistent, deciduous or marcescent, alternate (opposite or subopposite in Salix purpurea), spirally arranged, simple; stipules present or not; petiole present; blade margins toothed or entire, sometimes glandular. |
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Inflorescences | racemose or spicate, usually catkins, unbranched, sometimes fasciculate or racemelike cymes, flowering before or as leaves emerge or year-round; floral bract (1) subtending each flower, displaced onto pedicel or distinct, scalelike, apex entire, toothed, or laciniate; bract subtending pistillate flower deciduous or persistent. |
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Peduncles | present or absent. |
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Pedicels | present or absent. |
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Flowers | usually unisexual, sometimes bisexual, usually staminate and pistillate on different plants; sepals present or absent, or perianth modified into 1 or 2 nectaries, or a non-nectariferous disc; stamens 1–60(–70); filaments distinct or connate basally, slender; anthers longitudinally dehiscent; ovary 1, 2–7[–10]-carpellate, 1–7[–10]-locular; placentation usually parietal, sometimes axile on intruded, fused placentae; ovules 1–25 per ovary; style 1 per carpel, distinct or connate; stigmas 2–4, truncate, notched-capitate, or 2- or 3-lobed. |
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Staminate flowers | abaxial nectary 0.5–0.9 mm, adaxial nectary narrowly oblong, square, or ovate, 0.4–1.1 mm; anthers 0.6–1.1 mm. |
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Pistillate flowers | adaxial nectary oblong, ovate, or flask-shaped, 0.4–1.3 mm, longer than stipe; stipe 0–0.2 mm; ovary pyriform, pilose or villous to glabrescent, beak abruptly tapering to styles; ovules 12–24 per ovary; styles (± distinct) 0.2–0.5 mm; stigmas flat, abaxially non-papillate with pointed tip, or slenderly cylindrical, 0.3–1 mm. |
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Fruits | capsular, baccate, or drupaceous. |
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Seeds | sometimes surrounded by arillate coma of relatively long, silky hairs; endosperm scant or absent. |
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Catkins | staminate 7–42 × 4–9 mm, flowering branchlet 2–56 mm; pistillate densely or moderately densely flowered, slender to stout, 22–43 × 3–11 mm, flowering branchlet 2–55 mm; floral bract 1.4–2.6 mm, apex acute or convex, entire or erose, abaxially hairy throughout or proximally, hairs wavy, straight, or crinkled. |
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Salix exigua var. hindsiana |
Salicaceae |
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Phenology | Flowering mid Apr-mid May. | |||||||||||||
Habitat | Riparian, sandy-gravel floodplains | |||||||||||||
Elevation | 0-600 m (0-2000 ft) | |||||||||||||
Distribution |
CA; OR |
Nearly worldwide |
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Discussion | Variety hindsiana often is not distinguished from var. exigua. The two are difficult to separate morphologically even though var. hindsiana has been shown to have highly diverged chloroplast DNA (S. J. Brunsfeld et al. 1992). It can be distinguished from var. exigua by its soft, spreading hairs on branchlets and juvenile leaves (S. Brunsfeld, pers. comm.). Hybrids: Variety hindsiana forms natural hybrids with var. exigua. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Genera 50+, species ca. 1000 (4 genera, 123 species in the flora). Taxonomic placement of the Salicaceae and the genera included in it have varied greatly. Some botanists (H. G. A. Engler and K. Prantl 1887–1915) treated it as a primitive member of the Dicotyledoneae and grouped it with other families having simple, apetalous, unisexual flowers arranged in catkins, the “Amentiferae.” At about the same time, others (C. E. Bessey 1915) took a different view, regarding the simple flowers as the result of reduction, and placed the taxa in Caryophyllales. As early as 1905, H. Hallier could see that there were similarities between Salicaceae and Flacourtiaceae; at the time, he was vigorously challenged by E. Gilg (1915). A. D. J. Meeuse (1975) summarized evidence for a close relationship between these families, including wood anatomy, phytochemistry, host-parasite relationships (including rust fungi), and morphology. He concluded that the Salicaceae could be combined with the Flacourtiaceae, “perhaps as a tribe.” A. Cronquist (1988) and R. F. Thorne (1992b) placed the Salicaceae, in a narrow sense, in Violales near Flacourtiaceae. Molecular studies support a close relationship between Salicaceae and Flacourtiaceae in Malpighiales and show that Flacourtiaceae, in a broad sense, is paraphyletic. Based on a study of plastid rbcL DNA sequences, Salix and Populus were nested within a subset of 52 genera of Flacourtiaceae (M. W. Chase et al. 2002). Chase et al. proposed moving some genera from broadly circumscribed Flacourtiaceae to Salicaceae. Other studies, based on different gene sequences, came to the same conclusion (O. I. Nandi et al. 1998; V. Savolainen et al. 2000; K. W. Hilu et al. 2003; Angiosperm Phylogeny Group 2003). The discovery of the extinct fossil genus Pseudosalix (L. D. Boucher et al. 2003), from the Eocene Green River Formation of Utah, provided further support for placing some members of Flacourtiaceae in Salicaceae. The well-preserved Pseudosalix fossils, in which reproductive structures are directly associated with the leaves, occur intermixed with Populus fossils. The leaves are slender and have salicoid teeth, inflorescences are cymose, flowers are unisexual, pedicellate, tetrasepalous, and 3- or 4-carpellate, and seeds are comose, i.e., having characteristics intermediate between Salicaceae and Flacourtiaceae. The presence, in both families, of salicoid teeth is often cited in support of their close relationship (W. S. Judd 1997b; O. Nandi et al. 1998; M. W. Chase et al. 2002; H. P. Wilkinson 2007). Salicoid teeth were first recognized and defined as having the tip of the medial vein (seta) of the tooth retained as a dark, but not opaque, non-deciduous spherical callosity fused to the tooth apex and were reported to occur in Salicaceae and Idesia of the Flacourtiaceae (L. J. Hickey and J. A. Wolfe 1975). Nandi et al. reported that a broad survey of angiosperm leaves showed that salicoid teeth occur outside of Flacourtiaceae and Salicaceae only in Tetracentraceae. Isozyme and cytological evidence show that Populus and Salix are ancient polyploids (D. E. Soltis and P. S. Soltis 1990; Wang R. and Wang J. 1991). All Salix and Populus species contain salicin (R. T. Palo 1984). The genera often included in Salicaceae, in the narrow sense, are Chosenia, Populus, Salix (A. K. Skvortsov 1999), and, sometimes, Toisusu. Molecular studies (E. Leskinen and C. Alström-Rapaport 1999; T. Azuma et al. 2000) show that Chosenia is nested within Salix. H. Ohashi (2001) treated Toisusu as Salix subg. Pleuradinea Kimura and Chosenia as Salix subg. Chosenia (Nakai) H. Ohashi. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 7, p. 56. | FNA vol. 7, p. 3. | ||||||||||||
Parent taxa | ||||||||||||||
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Synonyms | S. hindsiana, S. exigua var. parishiana, S. hindsiana var. leucodendroides, S. hindsiana var. parishiana, S. macrostachya var. leucodendroides, S. parishiana, S. sessilifolia var. hindsiana, S. sessilifolia var. leucodendroides | |||||||||||||
Name authority | (Bentham) Dorn: Brittonia 50: 203. (1998) | Mirbel | ||||||||||||
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