Oenothera rosea |
Oenothera pallida |
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pink evening primrose, rose evening-primrose |
mountain evening primrose, pale evening-primrose, rockweed brush, white-stem evening primrose |
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Habit | Herbs perennial, caulescent, strigillose and often also sparsely hirsute; from slender taproot. | Herbs annual or perennial, glabrous, strigillose and/or villous, sometimes more villous distally, especially on flower parts; from a taproot, sometimes lateral roots producing adventitious shoots. | ||||||||||||
Stems | 1–several, ascending to decumbent, 7–65 cm. |
erect or ascending, single to several from base, unbranched or many-branched throughout, 10–50(–70) cm. |
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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. |
cauline, rosette usually weakly developed or absent, at least during flowering, sometimes well developed, 1–5(–7.8) × 0.3–1(–1.5) cm; petiole 0–2(–4.5) cm; blade lanceolate, oblong, linear-lanceolate, or ovate, margins subentire or remotely denticulate, deeply sinuate-dentate, or pinnatifid, sometimes repand. |
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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. |
1–several opening per day near sunset; buds nodding, weakly quadrangular, with free tips 0–2 mm; floral tube 15–40 mm; sepals 10–30 mm, not spotted; petals white, fading pink to deep pink, broadly obovate or obcordate, (10–)15–25(–40) mm; filaments 9–15 mm, anthers 3–10 mm; style 25–55 mm, stigma exserted beyond anthers at anthesis. |
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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. |
spreading to reflexed, straight to curved or contorted, cylindrical, obtusely 4-angled, tapering slightly from base to apex, 15–60 × 1.5–2.5 mm; sessile. |
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Seeds | narrowly obovoid, 0.5–0.9 × 0.3–0.5 mm. |
numerous, in 1 row per locule, brownish with dark spots or black, narrowly obovoid, 1.5–2.2 mm. |
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2n | = 14. |
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Oenothera rosea |
Oenothera pallida |
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Phenology | Flowering Mar–Sep. | |||||||||||||
Habitat | tropical areas.. | |||||||||||||
Elevation | 10–600 m. (0–2000 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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w North America; n Mexico; c North America
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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.) |
Subspecies 4 (4 in the flora). Oenothera pallida is a poorly understood species currently subdivided into four subspecies (W. L. Wagner et al. 2007) that differ largely in aspect, leaf division, capsule configuration, and pubescence. The variation pattern is rather complex with almost no diagnostic character uniformly distinguishing any one of the subspecies. Instead, each of the subspecies, which are mostly geographically separated although there is some level of overlap, have diagnostic suites of characters that maintain their linkage some of the time, but break down across the geographic area of each so that no single character uniquely identifies it. Each subspecies is characterized by leaf, pubescence, and, often, habit features. The issues with the integrity and intergradations of the subspecies are discussed below. Oenothera pallida has been determined to be self-incompatible (W. L. Wagner et al. 2007), but K. E. Theiss et al. (2010) determined that although most populations of subsp. pallida are self-incompatible, one near Salt Lake City is self-compatible. (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 | ||||||||||||||
Sibling taxa | ||||||||||||||
Subordinate 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 | Anogra pallida, O. albicaulis var. pallida | ||||||||||||
Name authority | L’Héritier ex Aiton: Hort. Kew. 2: 3. (1789) | Lindley: Bot. Reg. 14: plate 1142. (1828) | ||||||||||||
Web links |