Oenothera cavernae |
Oenothera gayleana |
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cave evening-primrose, cavedwelling evening primrose |
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Habit | Herbs winter or spring annual, acaulescent or short-caulescent, glandular puberulent, sometimes also sparsely hirsute; from a taproot. | Herbs perennial, sometimes suffrutescent, usually strigillose, sometimes glabrous; from a stout taproot. |
Stems | (when present) 1–several, ascending, usually unbranched, 2–4 cm. |
many, ascending to erect, branched from base, 15–30(–40) cm. |
Leaves | primarily in a basal rosette, sometimes also cauline, (0.5–)2.5–13(–19.5) × (0.2–)0.6–2.3(–2.7) cm; petiole 0.5–5.2 cm; blade oblanceolate to elliptic-oblanceolate (in some exceptionally large leaves), margins lyrate-pinnatifid to subentire (in very small ones), apex usually rounded, rarely acute. |
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. |
Flowers | 1–3(–10) per stem opening per day near sunset, without noticeable scent; buds sometimes ± recurved before anthesis; floral tube (20–)30–37(–47) mm; sepals 4.5–12 mm; petals white, fading pale pink, (6.5–)8–20(–25) mm; filaments 5.2–7.5(–12) mm, anthers (1.4–)3–4.5(–6) mm; style (24–)35–45(–56) mm, stigma surrounded by anthers at anthesis. |
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. |
Capsules | falcate (especially before maturity), ellipsoid-ovoid to ovoid, obtusely 4-angled, 12–38 × 6–14 mm, tapering to a sterile beak 2–8 mm, dehiscent to 1/2 their length, valve margins with a sinuate ridge or 8–20 nearly distinct tubercles; pedicel 0–10 mm. |
18–20 × 2 mm, hard, dehiscent 1/2 their length, often tardily dehiscent throughout their length. |
Seeds | usually numerous, sometimes as few as 5, in 2 adjacent rows per locule, obovoid, 2.5–3.1 × 1.1–1.4 mm, embryo 1/2 of seed volume, surface minutely papillose to reticulate; seed collar without membrane, producing a large empty cavity, margin irregularly sinuate. |
oblanceoloid, 1–1.8 mm, sharply angled, apex truncate. |
2n | = 14. |
= 14. |
Oenothera cavernae |
Oenothera gayleana |
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Phenology | Flowering Mar–May. | Flowering May–Sep. |
Habitat | Exposed calcareous slopes, crevices in limestone, dolomite, or loose talus, sandy arroyos, sandstone, granitic crevices, volcanic cinders in Mojave Desert or Great Basin scrub communities, rarely in arid juniper woodlands. | Gypsum outcrops. |
Elevation | 400–1700 m. (1300–5600 ft.) | 500–1400 m. (1600–4600 ft.) |
Distribution |
AZ; CA; NV |
NM; TX |
Discussion | Oenothera cavernae is known from the Arrow Canyon, Las Vegas, and Sheep ranges and the low hills near Arden and Sloan in Clark County, Nevada, eastward along the Grand Canyon to the vicinity of Page, Arizona, and perhaps Washington County, Utah and formerly in Glenn Canyon, and more recently collected in eastern San Bernardino County, California (eastern Clark Mountain Range, and the base of range in Ivanpah Valley). W. L. Wagner et al. (1985) determined O. cavernae to be self-compatible and autogamous. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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.) |
Source | FNA vol. 10. | FNA vol. 10. |
Parent taxa | ||
Sibling taxa | ||
Name authority | Munz: Leafl. W. Bot. 3: 50. (1941) | B. L. Turner & M. J. Moore: Phytologia 96: 200, figs. 1, 2. (2014) |
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