Oenothera deltoides |
Oenothera arida |
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basket evening-primrose, birdcage evening primrose, desert lantern, devil's lantern, dune primrose, hairy evening primrose, lion-in-a-cage |
trans-Pecos beeblossom |
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Habit | Herbs usually winter-annual, sometimes perennial, glabrous, glandular puberulent, strigillose, and/or villous, sometimes more villous distally, hairs sometimes very curly, especially on flower parts; from a taproot or relatively long, fleshy roots. | Herbs perennial, clumped, strigillose and glandular puberulent throughout, also sparsely villous; from stout roots. | ||||||||||||||||
Stems | central stem usually erect, usually thickened at base and spongy, branched or unbranched, branches few–several, slender, decumbent to ascending, from base, usually encircling central stem in older plants, 10–40(–100) cm. |
erect, usually branched several cm belowground or from near base, sometimes also branched distally, 20–60(–100) cm. |
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Leaves | in a basal rosette and cauline, rosette usually well developed (except subsp. howellii), basal 5–25 × 1–5 cm, cauline 4–12(–18) × 0.5–4 cm; petiole 1.5–8 cm; blade rhombic-obovate, lanceolate, or oblanceolate, margins subentire, dentate, or pinnatifid. |
in a basal rosette and cauline, basal 2–4 × 0.4–0.8 cm, petiole0–0.4 cm, blade narrowly oblanceolate to narrowly spatulate; cauline 0.5–5 × 0.1–0.8 cm, petiole 0–0.3 cm, blade narrowly lanceolate or very narrowly elliptic, margins subentire or sinuate-denticulate. |
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Flowers | 1–several opening per day near sunset; buds nodding, weakly or strongly quadrangular or fluted in distal 1/2, with free tips 0–9 mm; floral tube 20–40 mm; sepals (13–)15–35 mm, not spotted; petals white, fading pink to deep pink, broadly obovate or obcordate, 15–44 mm; filaments 8–15 mm, anthers 5–14 mm; style 35–60 mm, stigma exserted beyond anthers at anthesis. |
4-merous, nearly actinomorphic, opening near sunset; floral tube 9–13 mm; sepals 7–9 mm; petals white, fading pink to pale red, slightly unequal, rhombic, 7–8 mm, short-clawed; filaments 3–4 mm, anthers 4–5 mm, pollen 85–100% fertile; style 18–22 mm, stigma exserted beyond anthers at anthesis. |
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Capsules | spreading, straight to curved, becoming somewhat woody in age, cylindrical to slightly 4-angled, widest toward base, tapering from base to apex, (15–)30–80 × 1.5–5 mm; sessile. |
erect, fusiform, often slightly curved, weakly 4-angled, (9–)13–17 × 2–3 mm, valves with inconspicuous raised midrib; sessile. |
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Seeds | numerous, in 1 row per locule, buff with dark spots or black, narrowly obovoid, 1.5–2.8 mm. |
(1–)3 or 4, yellowish or light brown, 2–3.5 × 1–2 mm. |
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2n | = 14. |
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Oenothera deltoides |
Oenothera arida |
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Phenology | Flowering Apr–Aug. | |||||||||||||||||
Habitat | Sandy flats and washes. | |||||||||||||||||
Elevation | 1300–1800 m. (4300–5900 ft.) | |||||||||||||||||
Distribution |
w United States; nw Mexico
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TX; Mexico (Chihuahua) |
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Discussion | Subspecies 5 (5 in the flora). Oenothera deltoides is self-incompatible or self-compatible (W. M. Klein 1964; W. L. Wagner et al. 2007; K. E. Theiss et al. 2010). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Oenothera arida is known only from several areas in the foothills of the Davis Mountains in eastern Jeff Davis County, northeastern Presidio County, and northern Brewster County, and from areas near Gallego and Chihuahua in Chihuahua, Mexico. P. H. Raven and D. P. Gregory (1972[1973]) determined O. arida to be self-incompatible. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 10. | FNA vol. 10. | ||||||||||||||||
Parent taxa | Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Anogra | Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Gaura > subsect. Xerogaura | ||||||||||||||||
Sibling taxa | ||||||||||||||||||
Subordinate taxa | ||||||||||||||||||
Synonyms | Anogra deltoides | Gaura macrocarpa | ||||||||||||||||
Name authority | Torrey & Frémont in J. C. Frémont: Rep. Exped. Rocky Mts., 315. (1845) | W. L. Wagner & Hoch: Syst. Bot. Monogr. 83: 211. (2007) | ||||||||||||||||
Web links |