Chylismia claviformis subsp. yumae |
Onagraceae subfam. onagroideae |
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Yuma clavate fruit primrose |
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Habit | Herbs strigillose, often densely so, sometimes also glandular puberulent distally. | |
Stems | 5–40 cm. |
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Leaves | blade lateral lobes poorly or well developed, terminal lobe lanceolate, to 6.5 × 2 cm, margins irregularly sinuate-dentate. |
stipules present or absent. |
Flowers | opening at sunset; buds usually without free tips, sometimes with apical free tips less than 1 mm; floral tube orange-brown inside, 2.5–4 mm; petals pale yellow, fading reddish or not changing color, 3–5 mm. |
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. |
x |
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2n | = 14. |
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Chylismia claviformis subsp. yumae |
Onagraceae subfam. onagroideae |
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Phenology | Flowering Feb–May. | |
Habitat | Very arid dunes and sandy flats, with Ambrosia dumosa and Larrea tridentata. | |
Elevation | 0–300 m. (0–1000 ft.) | |
Distribution |
AZ; CA; Mexico (Baja California, Sonora) |
North America; Mexico; Central America; South America; West Indies; Eurasia; Pacific Islands (New Zealand, Society Islands); Australia |
Discussion | Subspecies yumae is known from southeastern Imperial County, California, Yuma Desert, Arizona, and from El Gran Desierto to Puerto Peñasco in northwestern Sonora, and in northeastern Baja California. The subspecies is probably from hybridization between subspp. aurantiaca and peirsonii; it intergrades with subsp. aurantiaca and rarely hybridizes with Chylismia brevipes subsp. arizonica. (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. |
Parent taxa | ||
Sibling taxa | ||
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Synonyms | Oenothera claviformis subsp. yumae, Camissonia claviformis subsp. yumae | |
Name authority | (P. H. Raven) W. L. Wagner & Hoch: Syst. Bot. Monogr. 83: 207. (2007) | W. L. Wagner & Hoch: Syst. Bot. Monogr. 83: 41. (2007) |
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