Oenothera stricta |
Oenothera primiveris |
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Chilean evening primrose |
desert evening primrose, yellow desert evening primrose |
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Habit | Herbs winter-annual, caulescent to short-caulescent, long-hirsute, hairs often with reddish purple pustulate bases, especially proximally, also moderately strigillose, and glandular puberulent distally, often on leaves; from a weakly fleshy taproot. | |
Stems | (when present) unbranched and erect or, sometimes, few branches from near base, in robust plants stems and caudex hollow and greatly enlarged, especially toward base, densely leafy, 5–35 cm. |
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Leaves | in a basal rosette, sometimes also cauline, (1.4–)6–15(–28) × (0.2–)1–3.5(–5.6) cm; petiole (0.9–)3.5–8(–14) cm; blade oblanceolate to linear-oblanceolate, pinnatifid or 2-pinnatifid to shallowly pinnately lobed, margins sinuate-dentate or subentire, apex obtuse. |
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Flowers | usually 1–4, rarely more, opening per day, 1–2 hours before sunset; sepals (7–)12–25(–30) mm; petals yellow, fading reddish orange to purple, obcordate to obovate, (6–)13–35(–40) mm; filaments 6–16 mm, anthers 3–10 mm; style (32–)40–90(–100) mm, stigma exserted beyond anthers or surrounded by them. |
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Capsules | woody in age, sigmoid or curved to nearly straight, lanceoloid to ovoid, 4-angled, 10–45(–60) × 4–8 mm, beak 4–15 mm, dehiscent 1/4–2/3 their length; sessile. |
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Seeds | usually numerous, in 2 rows per locule, obovoid to oblanceoloid, 3–3.5 × 1–1.4 mm, surface thickened above raphe and at distal end into U-shaped structure. |
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2n | = 14. |
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Oenothera stricta |
Oenothera primiveris |
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Phenology | Flowering Feb–May(–Jun). | |
Habitat | Sandy soil on flats, low hills and margins of sand dunes, along arroyos, roadsides, in desert scrub, grasslands and oak-grasslands. | |
Elevation | 30–1600 m. (100–5200 ft.) | |
Distribution |
South America [Introduced, California] |
AZ; CA; NM; NV; TX; UT; Mexico (Baja California, Chihuahua, Sonora)
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Discussion | Subspecies 2 (1 in the flora). Oenothera stricta is a PTH species and forms a ring of 14 chromosomes in meiosis, and is self-compatible and autogamous (W. Dietrich 1977). Subspecies stricta is naturalized in many areas around the world and may be so in California. Subspecies altissima W. Dietrich occurs only in Argentina. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Oenothera primiveris has a complex variation pattern (W. L. Wagner 2005). In the western part of the range from southeastern California across southern Nevada to southern Utah counties of Emery, Kane, and Washington, and northwestern Mohave County, Arizona, plants generally have a gray appearance, with dense pubescence and larger flowers with widespread self-compatibility, but with scattered populations retaining self-incompatibility. Populations from southof the Mogollon Plateau to southern New Mexico, western Texas, Chihuahua, Sonora, and Baja California, Mexico, are greener in appearance with smaller to much smaller flowers, and are all self-compatible with occasional outcrossing or complete autogamy. The transitions between these two extremes are so extensive and more or less gradual that it is not possible to subdivide into two subspecies as has been done previously (Wagner). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 10. | FNA vol. 10. |
Parent taxa | Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Oenothera > subsect. Munzia > ser. Allochroa | Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Eremia |
Sibling taxa | ||
Subordinate taxa | ||
Synonyms | Lavauxia lobata, L. primiveris, O. bufonis, O. cespitosa var. primiveris, O. johnsonii, O. primiveris subsp. bufonis, O. primiveris var. bufonis, O. primiveris subsp. caulescens, O. primiveris var. caulescens, Pachylophus johnsonii | |
Name authority | Ledebour ex Link: Enum. Hort. Berol. Alt. 1: 377. (1821) — (as striata) | A. Gray: Smithsonian Contr. Knowl. 5(6): 58. (1853) |
Web links |