Oenothera gayleana |
Oenothera flava |
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long-tubed evening primrose, yellow evening primrose |
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Habit | Herbs perennial, sometimes suffrutescent, usually strigillose, sometimes glabrous; from a stout taproot. | Herbs perennial, rarely short-lived, acaulescent or very short-caulescent, glabrate to moderately strigillose, usually also glandular puberulent, sometimes sparsely hirsute distally; from a taproot. |
Stems | many, ascending to erect, branched from base, 15–30(–40) cm. |
(when present) ascending, 1–several, usually densely leafy, 0–2 cm. |
Leaves | 2.5–3.5 × 0.1–0.2 cm, rarely fascicles of small leaves present in non-flowering axils; petiole 0–0.1 cm; blade linear to narrowly linear-lanceolate, folded lengthwise, base long-attenuate, margins subentire or serrulate, apex acute. |
primarily in a basal rosette, (3.4–)6–30(–36) × (0.5–)1.5–5(–7) cm, flexible, sometimes ± fleshy; petiole (0.2–)2–7(–10) cm; blade oblanceolate to linear, margins usually irregularly and coarsely pinnately lobed, rarely subentire, apex acute. |
Flowers | opening near sunrise; buds with free tips 0–0.5 mm; floral tube 7 mm; sepals 4–6 mm, midribs keeled; petals yellow, fading yellow to orange, 15–20 mm; antisepalous filaments 5 mm, antipetalous filaments 2 mm, anthers 3–4 mm, pollen 90–100% fertile; style 10 mm, stigma discoid to quadrangular, exserted beyond anthers at anthesis. |
1–4 opening per day near sunset; buds with free tips (1–)2–10(–12) mm; floral tube (24–)40–200(–265) mm; sepals (8–)11–40(–42) mm; petals bright yellow, sometimes paler (in smaller-flowered plants), fading pale orange, drying purple, (7–)10–45(–50) mm; filaments (5–)8–23(–26) mm, anthers (2–)3–13(–16) mm; style (40–)50–250(–290) mm, stigma exserted beyond or surrounded by ring of anthers. |
Capsules | 18–20 × 2 mm, hard, dehiscent 1/2 their length, often tardily dehiscent throughout their length. |
leathery in age, surface usually conspicuously reticulate, usually narrowly ovoid or ellipsoid, sometimes ovoid or lanceoloid, winged, wings narrowly oblong, (2–)3–5(–6) mm wide, confined to distal 2/3 of capsule, (10–)20–35(–43) × 4–8 mm (excluding wings), gradually constricted to a short beak, dehiscent 1/4–1/2 their length, valve surface usually conspicuously reticulate; sessile. |
Seeds | oblanceoloid, 1–1.8 mm, sharply angled, apex truncate. |
asymmetrically cuneiform, 1.8–2.2(–2.6) mm.2n = 14. |
2n | = 14. |
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Oenothera gayleana |
Oenothera flava |
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Phenology | Flowering May–Sep. | Flowering Mar–Aug(–Oct). |
Habitat | Gypsum outcrops. | Local and colonial, sometimes abundant in wet (at least seasonally moist) clay to gravelly sand of swales, desiccating flats and ponds, montane meadows, margins of permanent or seasonal watercourses, open sites. |
Elevation | 500–1400 m. (1600–4600 ft.) | 300–3200 m. (1000–10500 ft.) |
Distribution |
NM; TX |
AZ; CA; CO; ID; MT; ND; NE; NM; NV; OR; SD; UT; WA; WY; AB; MB; SK; Mexico (Chihuahua, Durango, Guanajuato, Hidalgo, Jalisco, Sonora)
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Discussion | Oenothera gayleana is a recently discovered gypsum endemic known only from scattered outcrops from De Baca and Eddy counties in New Mexico, and Culberson County in Texas. When published, the delimitation of O. gayleana included populations in Collinsworth and Dickens counties in the Texas panhandle, and adjacent Harmon County in Oklahoma. Subsequent study (B. Cooper et al., unpubl.) has determined they are actually O. serrulata. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Petals in Oenothera flava typically range from 7–32 mm with floral tubes 24–100 mm; however, plants from three disjunct areas: the Mogollon Plateau in Arizona to Catron County, New Mexico; Sacramento Mountains and Sierra Blanca, Lincoln and Otero counties, New Mexico; and the Sierra Madre Occidental from northern Chihuahua south to Durango, have much larger petals (30–55 mm) and longer floral tubes (80–265 mm). They were originally recognized as a distinct species or most recently as a subspecies (O. flava subsp. taraxacoides), but detailed study of the variation pattern suggests that the larger flowers occur in areas of high hawkmoth species diversity and higher rates of outcrossing, similar to the pattern discussed in detail by D. P. Gregory (1963, 1964). R. A. Raguso et al. (2007) and H. E. Summers et al. (2015) came to the same conclusion in an independent study of floral biology of sect. Lavauxia. Because populations from the three disjunct areas appear to have diverged independently from lower-elevation source populations, it seems best to treat the complex as one variable species without any formal subdivision. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 10. | FNA vol. 10. |
Parent taxa | ||
Sibling taxa | ||
Synonyms | Lavauxiaflava a., L. palustris, L. taraxacoides, O. flava subsp. taraxacoides, O. murdockii, O. taraxacoides, O. triloba var. ecristata | |
Name authority | B. L. Turner & M. J. Moore: Phytologia 96: 200, figs. 1, 2. (2014) | (A. Nelson) Garrett: Spring Fl. Wasatch ed. 4, 106. (1927) |
Web links |
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