Oenothera deltoides |
Oenothera glazioviana |
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basket evening-primrose, birdcage evening primrose, desert lantern, devil's lantern, dune primrose, hairy evening primrose, lion-in-a-cage |
garden evening-primrose, large-flower evening primrose, red-sepal evening-primrose |
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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 biennial, densely to sparsely strigillose and villous, with spreading, red-pustulate hairs, also glandular puberulent and with only a few appressed hairs near inflorescence. | ||||||||||||||||
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, green or flushed with red on proximal parts, sometimes inflorescence axis red, usually withside branches obliquely arising from rosette and secondary branches from main stem, 50–150 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 13–30 × 3–5 cm, cauline 5–15 × 2.5–4 cm; blade dark to bright green, white- or red-veined, narrowly oblanceolate to oblanceolate, sometimes narrowly elliptic to lanceolate distally, margins usually conspicuously crinkled, sometimes undulate, bluntly dentate, teeth widely spaced, sometimes sinuate-dentate proximally or lobed; bracts persistent. |
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Inflorescences | erect, unbranched. |
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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. |
opening near sunset; buds erect, 7–9 mm diam., with free tips terminal, erect to spreading, 5–8 mm; floral tube 35–50 mm; sepals yellowish green, usually flushed with red or red-striped, sometimes very dark red throughout, 28–45 mm; petals yellow to pale yellow, fading yellowish white and somewhat translucent, very broadly obcordate, 35–50 mm; filaments 17–25 mm, anthers 10–12 mm, pollen ca. 50% fertile; style 50–80 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 or slightly spreading, dull green when dry, lanceoloid, 20–35 × 5–6 mm, free tips of valves 0.8–1.5 mm. |
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Seeds | numerous, in 1 row per locule, buff with dark spots or black, narrowly obovoid, 1.5–2.8 mm. |
1.3–2 ×1–1.5 mm, ca. 50% abortive. |
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2n | = 14. |
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Oenothera deltoides |
Oenothera glazioviana |
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Phenology | Flowering (Jun–)Jul–Sep(–Oct). | |||||||||||||||||
Habitat | Open, disturbed sites. | |||||||||||||||||
Elevation | 20–600(–1400) m. (100–2000(–4600) ft.) | |||||||||||||||||
Distribution |
w United States; nw Mexico
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AL; AR; CA; CT; IL; IN; MA; ME; MI; MT; NC; NH; NJ; NY; OR; PA; RI; VT; WA; WI; WV; BC; MB; NS; ON; QC [Introduced in North America; introduced nearly worldwide in temperate and subtropical regions]
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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 glazioviana originated by hybridization between two cultivated or naturalized species in Europe and was introduced into the horticultural trade by Carter and Company of England in 1860 (R. E. Cleland 1972; P. H. Raven et al. 1979). The oldest name applied to this entity was based on plants cultivated in Rio de Janeiro in 1868; clearly, O. glazioviana must have spread very rapidly. Oenothera glazioviana is a PTH species and forms a ring of 12 chromosomes and 1 bivalent in meiosis, and is self-compatible and autogamous (W. Dietrich et al. 1997). It has plastome II or III and a AB genome composition. (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. Oenothera > subsect. Oenothera | ||||||||||||||||
Sibling taxa | ||||||||||||||||||
Subordinate taxa | ||||||||||||||||||
Synonyms | Anogra deltoides | O. erythrosepala, O. grandiflora subsp. erythrosepala, Onagra erythrosepala | ||||||||||||||||
Name authority | Torrey & Frémont in J. C. Frémont: Rep. Exped. Rocky Mts., 315. (1845) | Micheli in C. F. P. von Martius et al.: Fl. Brasil. 13(2): 178. (1875) | ||||||||||||||||
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