Clarkia lingulata |
Onagraceae subfam. onagroideae |
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Merced clarkia |
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Stems | erect, to 60 cm, puberulent. |
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Leaves | petiole to 15 mm; blade linear to narrowly lanceolate, 2–6 cm. |
stipules present or absent. |
Flowers | floral tube 1–4 mm; sepals reflexed together to 1 side; corolla rotate, petals bright pink, red-flecked or not, oblanceolate, 10–20 mm, apex subentire or minutely notched; stamens 8, unequal, outer anthers lavender, inner smaller, paler. |
floral tube present or, rarely, absent; sepals 2 or 4 (very rarely 3), deciduous with floral tube, petals, and stamens; petals yellow, white, pink, red, rarely in combination. |
Capsules | 10–20 mm. |
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Seeds | brown, 1 mm, minutely scaly to puberulent, crest inconspicuous. |
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Inflores | -cences open racemes, axis recurved at tip in bud; buds pendent. |
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x |
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2n | = 18. |
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Clarkia lingulata |
Onagraceae subfam. onagroideae |
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Phenology | Flowering May–Jun. | |
Habitat | Open chaparral. | |
Elevation | 400–500 m. (1300–1600 ft.) | |
Distribution |
CA |
North America; Mexico; Central America; South America; West Indies; Eurasia; Pacific Islands (New Zealand, Society Islands); Australia |
Discussion | Clarkia lingulata is listed as endangered by the State of California, known from only a few populations in Merced River Canyon, Mariposa County. It is derived from C. biloba subsp. australis, from which it can be distinguished morphologically by its narrower, unlobed petals; the two taxa also differ in chromosome number, and form only highly sterile hybrids. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Genera 21, species 582 (16 genera, 246 species in the flora). Onagroideae encompass the main lineage of the family, after the early branching of Ludwigia (R. A. Levin et al. 2003, 2004). This large and diverse lineage is distinguished by the presence of a floral tube beyond the apex of the ovary; sepals deciduous with the floral tube, petals, and stamens; pollen shed in monads (or tetrads in Chylismia sect. Lignothera and all but one species of Epilobium); ovular vascular system exclusively transseptal (R. H. Eyde 1981); ovule archesporium multicellular (H. Tobe and P. H. Raven 1996); and change in base chromosome number from x = 8 in Ludwigia to x = 10 or x = 11 at the base of Onagroideae (Raven 1979; Levin et al. 2003). Molecular work (Levin et al. 2003, 2004) substantially supports the traditional tribal classification (P. A. Munz 1965; Raven 1979, 1988); tribes are recognized to delimit major branches within the phylogeny of Onagroideae, where the branches comprise strongly supported monophyletic groups of one or more genera. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 10. | FNA vol. 10. |
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Sibling taxa | ||
Subordinate taxa | ||
Name authority | H. Lewis & M. E. Lewis: Madroño 12: 35. (1953) | W. L. Wagner & Hoch: Syst. Bot. Monogr. 83: 41. (2007) |
Web links |