Allium amplectens |
Allium fimbriatum |
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narrow-leaf onion, slim-leaf onion |
fringe onion, wild onion |
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Bulbs | 1–15+, increase bulbs absent or ± equaling parent bulbs, never appearing as basal cluster, not clustered on stout primary rhizome, ovoid to ± globose, 0.6–1.5 × 0.6–1.3 cm; outer coats enclosing 1 or more bulbs, brown, prominently cellular-reticulate, membranous, cells in ± vertical rows, forming irregular herringbone pattern, transversely elongate, V-shaped, without fibers; inner coats usually dark red, sometimes white to pink, cells obscure, quadrate. |
1–3, not clustered on stout, primary rhizome, ovoid to ± globose, 1–1.7 × 0.8–1.7 cm; outer coats enclosing 1 or more bulbs, reddish brown, membranous, lacking cellular reticulation or cells arranged in only 2–3 rows proximal to roots, ± quadrate, without fibers; inner coats pale brown to white, cells obscure, quadrate. |
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Leaves | persistent, withering from tip at anthesis, 2–4, basally sheathing, sheaths not extending much above soil surface; blade solid, subterete or ± channeled, 10–36 cm × 0.5–2 mm, margins entire. |
persistent, withering from tip by anthesis, 1, basally sheathing, sheath not extending much above soil surface; blade solid, terete, 12–50 cm × 1–4 mm. |
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Scape | persistent, solitary, erect, solid, terete, 15–50 cm × 3–5 mm. |
persistent, solitary, erect, solid, terete, 10–35 cm × 0.5–3.5 mm. |
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Umbel | shattering after seeds mature, each flower deciduous with its pedicel as a unit, erect, compact, 10–50-flowered, hemispheric, bulbels unknown; spathe bracts persistent, 2–3, 6–13-veined, ovate, ± equal, apex short-acuminate. |
persistent, erect, compact, 6–75-flowered, hemispheric, bulbils unknown; spathe bracts persistent, 2–3, 4–7-veined, lanceolate to ovate, ± equal, apex attenuate to setaceous. |
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Flowers | stellate, 5–9 mm; tepals spreading at anthesis, white to pink, lanceolate, ± equal, becoming papery and connivent over capsule, margins entire, apex acute; stamens included; anthers yellow or purple; pollen yellow; ovary crested; processes 6, lateral, ± prominent, ± rectangular, margins entire; style linear, equaling stamens; stigma capitate, scarcely thickened, unlobed; pedicel 4–16 mm. |
urceolate to campanulate, 6–12 mm; tepals erect, dark reddish purple to pale lavender, or white, lanceolate to ovate, ± equal, becoming ± rigid to papery in fruit, margins entire or denticulate with few minute teeth near tip, apex acute to acuminate, recurved-spreading or not at tip; stamens included; anthers yellow; pollen yellow; ovary usually crested (rarely crestless); processes 6, prominent, ± triangular, margins denticulate to laciniate; style linear, equaling stamens; stigma capitate, 3-lobed, lobes slender, recurved; pedicel 6–20 mm. |
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Seed | coat dull; cells minutely roughened. |
coat dull; cells minutely roughened. |
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2n | = 14, 21, 28. |
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Allium amplectens |
Allium fimbriatum |
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Phenology | Flowering Apr–Jul. | |||||||||
Habitat | Clay soils, including serpentine, dry slopes, and open plains | |||||||||
Elevation | 0–1800 m (0–5900 ft) | |||||||||
Distribution |
CA; OR; WA; BC
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CA; Mexico (Baja California)
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Discussion | All three chromosome races of Allium amplectens are widespread. The triploids are achiasmatic, causing a breakdown in the first meiotic division. This is followed by a normal second division resulting in pollen dyads that are, presumably, nonfunctional; seeds are produced by apomixis. The diploids and tetraploids produce normal pollen, in tetrads, that appears to be functional. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Varieties 3 (3 in the flora). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 26, p. 262. | FNA vol. 26, p. 254. | ||||||||
Parent taxa | Liliaceae > Allium | Liliaceae > Allium | ||||||||
Sibling taxa | ||||||||||
Subordinate taxa | ||||||||||
Synonyms | A. acuminatum var. gracile, A. attenuifolium, A. attenuifolium var. monospermum, A. monospermum, A. occidentale, A. serratum | |||||||||
Name authority | Torrey: Pacif. Railr. Rep. 4(5): 148. (1857) | S. Watson: Proc. Amer. Acad. Arts 14: 232. (1879) | ||||||||
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