Salix alaxensis var. longistylis |
Salicaceae |
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Alaska willow, feltleaf willow, glaucous Alaska willow |
willow family |
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Habit | Shrubs or trees, 1–4 m. Stems: branches yellow-brown or red-brown, glabrous or sparsely villous; branchlets strongly glaucous, glabrescent or sparsely villous. | 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 | 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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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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Largest | medial leaves: midrib prominent, sparsely pubescent to glabrescent, abaxial surface noticeably glaucous or not. |
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Catkins | pistillate 37–103 × 8–20 mm, flowering branchlet 0–13 mm. |
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Salix alaxensis var. longistylis |
Salicaceae |
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Phenology | Flowering late Mar-early Jul. | |||||||||||||
Habitat | Pioneer thickets on river alluvium and glacial moraines, subalpine thickets, alpine tundra, moist to mesic talus slopes, forest openings | |||||||||||||
Elevation | 0-2000 m (0-6600 ft) | |||||||||||||
Distribution |
AK; BC; MB; NT; YT |
Nearly worldwide |
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Discussion | Variety longistylis differs from var. alaxensis mainly in its glaucous and less densely hairy branchlets. Some specimens of var. alaxensis, in which the indumentum has been partially removed by wind erosion, show that they, too, have glaucous branchlets. The only fundamental difference between the two may be density of branchlet indumentum. Other differences, which appear in varietal descriptions, may represent inadequate sampling. These taxa sometimes intergrade and var. longistylis may not be worthy of taxonomic recognition. It is included here only because of very conspicuous differences between the extremes. Hybrids: Variety longistylis forms natural hybrids with Salix sitchensis. Variety longistylis × Salix sitchensis grows with both parents at the mouth of the Twentyfour Mile River, south-central Alaska. The plants resemble var. longistylis in having relatively long styles and stigmas, oblong nectaries, and sparsely hairy branchlets, and S. sitchensis in having brittle branches, weakly glaucous branchlets, hairs sparse and crinkled, and ovaries with straight hairs. Fruits were set but no seed developed. (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. 147. | FNA vol. 7, p. 3. | ||||||||||||
Parent taxa | ||||||||||||||
Sibling taxa | ||||||||||||||
Subordinate taxa | ||||||||||||||
Synonyms | S. longistylis, S. alaxensis subsp. longistylis | |||||||||||||
Name authority | (Rydberg) C. K. Schneider: J. Arnold Arbor. 1: 225. (1920) | Mirbel | ||||||||||||
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