Camassia |
Camassia quamash |
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camas, quamash |
camas, common camas, small camas |
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Habit | Herbs, perennial, from bulbs. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bulbs | solitary or clustered, tunicate, ovoid to globose; tunic black or brown. |
seldom clustered, globose, 1–5 cm diam. |
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Leaves | basal, appearing whorled; blade linear, keeled. |
usually fewer than 10, 1–6 dm × 4–20 mm. |
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Inflorescences | appearing terminal, racemose, bracteate; bracts sterile or subtending flowers, narrowly lanceolate. |
20–80 cm; sterile bracts absent, bracts subtending flowers usually equaling or exceeding pedicel. |
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Flowers | actinomorphic or zygomorphic; tepals 6, persistent, ± equal in 2 whorls of 3, distinct, violet, blue, or white, each 3–9-veined, lanceolate, ± twisted in drying; stamens 6; filaments inserted on receptacles at base of tepals, slender; anthers versatile, dehiscence introrse; ovary 3-locular, septal nectaries present, ovules 6–36; style filiform; stigma 3-lobed; pedicel spreading to incurving-erect in fruit. |
usually zygomorphic, sometimes actinomorphic; tepals withering separately or connivent over capsules after anthesis, long-persistent on fruiting racemes, blue or bluish violet, each 3–9-veined, 12–35 × 1.5–8 mm; anthers usually yellow, sometimes bluish violet, violet, or brown, 2.5–7 mm; fruiting pedicel mostly incurving-erect, occasionally spreading-erect, 5–70 mm. |
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Fruits | capsular, ovoid to ellipsoid or subglobose, dehiscence loculicidal. |
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Capsules | not deciduous, pale green to pale brown, ovoid, 6–19 mm. |
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Seeds | 6–36, lustrous black, obpyriform to ovoid-ellipsoid, 2–4 mm. |
5–10 per locule. |
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x | = 15. |
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2n | = 30. |
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Camassia |
Camassia quamash |
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Distribution |
North America |
w United States and Canada
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Discussion | Species 6 (6 in the flora). Cmassia has been associated with other western North American genera of Liliaceae such as Schoenolirion, Hastingsia, and especially Chlorogalum (F. Speta 1998; M. Pfosser and F. Speta 1999), but recent molecular evidence (D. J. Bogler and B. B. Simpson 1996; M. F. Fay and M. W. Chase 1996) suggests that it may be related instead to the Agavaceae. Furthermore, the bimodal, 2n = 30 karyology of Camassia (A. Fernandez and J. R. Davina 1991) is similar to that of Agavaceae (D. Satô 1935) and not that of Chlorogalum. Camassia bulbs have been an important food staple for native Americans, especially in the Pacific Northwest (G. R. Downing and L. S. Furniss 1968; N. J. Turner and H. V. Kuhnlein 1983), where bulbs were dug and traded on large encampment meadows. Similarity to the poisonous bulbs of Zigadenus (“death camas”) is a concern where ranges of the two genera overlap. Several Camassia species are cultivated and represent a major horticultural contribution from the native flora. Variation and intergradation of C. angusta and C. scilloides have been reviewed by T. A. Ranker and A. F. Schnabel (1986), as well as J. A. Steyermark (1961), R. O. Erickson (1941), and F. W. Gould (1942). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
camassia quamash is highly variable morphologically. although there tend to be distinct geographical variants. here recognized as subspecies following f. w. gould (1942), there is much overlap among them. the subspecific status of these taxa is retained to highlight the extreme morphological variability and geographical patterns within the species. a detailed biosystematic study of this complex is needed Subspecies 8 (8 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. 303. | FNA vol. 26, p. 304. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Synonyms | Phalangium quamash | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | Lindley: Edwards’s Bot. Reg. 18: plate 1486. (1832) | (Pursh) Greene: Man. Bot. San Francisco, 313. (1894) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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