Oenothera rosea |
Oenothera suffrutescens |
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pink evening primrose, rose evening-primrose |
linda tarde, scarlet beeblossom, scarlet evening-primrose, scarlet gaura, wild honeysuckle |
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Habit | Herbs perennial, caulescent, strigillose and often also sparsely hirsute; from slender taproot. | Herbs perennial, densely strigillose, sometimes also long-villous proximally, sometimes glabrate; from a deep, thick taproot, often with branching underground stems, or branching only at surface, these often becoming horizontal or nearly so and giving rise to new plants. |
Stems | 1–several, ascending to decumbent, 7–65 cm. |
erect or ascending, usually many-branched, 10–120 cm. |
Leaves | in a basal rosette and cauline, basal 1–6 × 0.3–2 cm, blade narrowly elliptic to elliptic or ovate, margins subentire, weakly serrulate, or sinuate-pinnatifid; cauline 1–6 × 0.3–2 cm, blade narrowly elliptic to narrowly ovate, margins subentire or weakly serrulate, proximal ones sinuate-pinnatifid. |
in a basal rosette (but not present at flowering) and cauline, 0.7–6.5 × 0.1–1.5 cm, blade linear to narrowly elliptic, margins entire or remotely and coarsely serrate. |
Inflorescences | erect. |
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Flowers | 1–3 opening per day near sunrise; buds with free tips 0.1–1 mm; floral tube 4–8 mm; sepals 6–12 mm; petals rose purple, fading darker, 4–12 mm; filaments 4–6 mm, anthers 2–3.5 mm, pollen 35–65% fertile; style 7–13.5 mm, stigma surrounded by anthers at anthesis. |
4-merous, zygomorphic, opening near sunset; floral tube 4–11(–13) mm; sepals 5–9(–10) mm; petals white, fading salmon pink to scarlet-red, slightly unequal, obovate to elliptic-obovate or elliptic, 3–7(–8) mm, abruptly clawed; filaments 3–6.5(–7) mm, anthers (2.5–)3–5(–5.5) mm; style 10–22 mm, stigma exserted beyond anthers at anthesis. |
Capsules | narrowly obovoid, 4–12 × 2–4 mm, apex attenuate to a sterile beak, proximal stipe 5–20 mm, gradually tapering to base, valve midrib prominent in distal part; sessile. |
erect, pyramidal in distal 1/2 and abruptly constricted to terete proximal part, pyramidal part weakly or strongly angled, not conspicuously bulging at base, 4–9 × (1–)1.5–3 mm; sessile. |
Seeds | narrowly obovoid, 0.5–0.9 × 0.3–0.5 mm. |
(1–)3 or 4, light to reddish brown, 1.5–3 × 1–1.5 mm. |
2n | = 14. |
= 14, 28, 42, 56. |
Oenothera rosea |
Oenothera suffrutescens |
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Phenology | Flowering Mar–Sep. | Flowering Apr–Aug(–Nov). |
Habitat | tropical areas.. | Sandy or clay soil, often calcareous, desert shrublands to pinyon-juniper or oak woodlands, grasslands, disturbed areas. |
Elevation | 10–600 m. (0–2000 ft.) | 150–2000(–3000) m. (500–6600(–9800) ft.) |
Distribution |
AZ; CA; TX; Mexico; Central America; West Indies; tropical areas [Introduced in South America (Argentina), Europe, Asia, s Africa, Atlantic Islands (Azores, Canary Islands)]
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AZ; CA; CO; IA; IL; IN; KS; MI; MN; MO; MT; ND; NE; NM; NV; NY; OK; SD; TX; UT; WI; WY; AB; BC; MB; ON; SK; Mexico (Aguascalientes, Chihuahua, Coahuila, Durango, Guanajuato, Hidalgo, Jalisco, México, Nuevo León, Oaxaca, Puebla, San Luis Potosí, Sonora, Tamaulipas, Veracruz, Zacatecas); introduced in South America (Brazil); Europe (Wales)
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Discussion | Oenothera rosea is a PTH species, forming a ring of 14 chromosomes in meiosis, and is self-compatible and autogamous. In the flora area, it is known from Cochise, Pima, and Santa Cruz counties in Arizona, Alameda, Los Angeles, Riverside, San Bernardino, San Diego, San Francisco, and Santa Barbara counties in California (primarily in urban areas), and from southern Texas. It is clearly of North American origin, since all of its close relatives are confined to North America, and has spread south along the Andes. It occurs at 500–3700 m in South America but generally at lower elevations in most areas. The name Hartmannia affinis Spach is illegitimate, being based on Oenothera virgata; H. gauroides Spach is also illegitimate, being based on O. rosea; O. purpurea Lamarck is a later homonym; these three names pertain here. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Oenothera suffrutescens is naturalized sporadically in southern California (Los Angeles, San Diego, Santa Barbara, and Ventura counties; although native in eastern part of the state), Illinois, Indiana, Michigan, New York, southern Ontario, and Wisconsin. P. H. Raven and D. P. Gregory (1972[1973]) determined Oenothera suffrutescens to be self-incompatible and polyploid. It is known to form hybrids with O. calcicola and O. hispida. Schizocarya kunthii Spach is an illegitimate name based on Gaura epilobioides that pertains here. (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. Hartmannia | Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Gaura > subsect. Campogaura |
Sibling taxa | ||
Synonyms | Gaura epilobia, Godetia heuckii, Hartmannia rosea, H. rosea var. parvifolia, H. virgata, O. psycrophila, O. rosea var. parvifolia, O. rubra, O. virgata, Xylopleurum roseum | Gaura suffrutescens, G. bracteata, G. coccinea, G. coccinea var. arizonica, G. coccinea var. epilobioides, G. coccinea var. glabra, G. coccinea var. integerrima, G. coccinea var. parvifolia, G. epilobioides, G. glabra, G. induta, G. linearis, G. marginata, G. multicaulis, G. odorata, G. parvifolia, G. spicata |
Name authority | L’Héritier ex Aiton: Hort. Kew. 2: 3. (1789) | (Seringe) W. L. Wagner & Hoch: Syst. Bot. Monogr. 83: 214. (2007) |
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