Asarum wagneri |
Asarum |
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green-flower wild ginger, long-tail wild ginger, wagner's wild ginger |
asaret, gingembre sauvage, wild-ginger |
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Habit | Herbs, perennial, deciduous, rhizomatous, without aerial stems. | |||||||||||||||||||||
Rhizomes | horizontal, ± deeply buried, internodes 0.5-2.1 cm. |
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Leaves | blade not variegate, broadly reniform to cordate-reniform, 3-8 × 4-11 cm, apex obtuse to rounded (broadly acute); surfaces abaxially sparsely hirsute, adaxially sparsely hirsute only along veins, marginal hairs mostly curved toward apex. |
blade membranous or leathery, pubescent at least abaxially and on margins. |
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Inflorescences | terminal on rhizome, flowers solitary; bracts absent. |
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Flowers | erect or ascending; peduncle 0.8- calyx tube subglobose to cylindric-urceolate or urceolate, externally light green, sparsely to moderately hirsute, internally white or light green, bordered and occasionally striped with purple, with purple hairs; distal portion of sepal spreading perpendicularly from base at anthesis, bent abruptly upward at midpoint, 8-20 mm, apex filiform-acuminate, abaxially white to pale green, sparsely villous to villous, adaxially white or light green, at least distally, bordered with purple and occasionally with purple band across base, puberulent with crisped purple-tipped hairs; pollen sacs 1-2 mm, sterile tip of connective on inner stamens dark red, 0.25-1 mm, shorter than pollen sacs. |
sepals distinct, usually mixture of white, green, tan, red, or purple, proximally touching valvately and forming well-de tube, externally usually villous, inner surface strigose, smooth or with weak longitudinal ribs, never with network of low ridges; vestigial petals present or absent; stamens 12, distinct; filaments longer than pollen sacs; terminal appendage of anther well developed; ovary inferior, 6-locular; styles connate in column. |
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Capsule | fleshy, dehiscence irregular. |
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Seeds | ovoid, not winged, with fleshy appendage. |
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x | = 13. |
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Asarum wagneri |
Asarum |
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Phenology | Flowering spring–summer (May–Jul). | |||||||||||||||||||||
Habitat | Understory of Abies forests and open boulder fields in Tsuga forests near timberline | |||||||||||||||||||||
Elevation | 1500-3200 m (4900-10500 ft) | |||||||||||||||||||||
Distribution |
OR
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North America; Eurasia |
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Discussion | Asarum wagneri is endemic to the Cascade Range of pouthern Oregon (K. L. Lu and M. R. Mesler 1983). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Species ca. 10 (6 in the flora). The species seem amply distinct, but herbarium material can be difficult to key for several reasons. First, the diagnostic colors of some organs (especially of the connective and the inner hairs of the calyx) often darken on drying. Second, immature flowers and young fruit are superficially similar to mature flowers, but color and posture of floral organs may be different at those stages. For instance, posture of the distal portion of sepals at anthesis (whether erect, spreading, or reflexed) is diagnostic for the species, but sepals in all species are erect in bud and in fruit. Third, as in Hexastylis, distortion of the flower in pressing makes it difficult to interpret calyx structure. In particular, the distinction between proximal portions of the sepals, which meet valvately to form a well-defined false calyx tube, and distal portions, which do not, is obvious in fresh material but often unclear in the herbarium. The flowers of Asarum are predominantly self-pollinated, but they are occasionally visited by mycotrophic flies (K. L. Lu 1982). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 3. | FNA vol. 3. | ||||||||||||||||||||
Parent taxa | Aristolochiaceae > Asarum | Aristolochiaceae | ||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||
Synonyms | A. caudatum var. viridiflorum | |||||||||||||||||||||
Name authority | K. L. Lu & Mesler: Brittonia 35: 331. (1983) | Linnaeus: Sp. Pl. 1: 442. 175: Gen. Pl. ed. 5, 201. (1754) | ||||||||||||||||||||
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