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Wolf's evening-primrose

long-tubed evening primrose, yellow evening primrose

Habit Herbs biennial or short-lived perennial, densely strigillose, also villous with spreading to subappressed hairs, hairs sometimes pustulate, also glandular puberulent distally. 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

erect, green, flushed with red proximally or red throughout, unbranched or branches obliquely arising from rosette and sometimes secondary branches arising from main stem, 50–100 cm.

(when present) ascending, 1–several, usually densely leafy, 0–2 cm.

Leaves

in a basal rosette and cauline, basal 13–35 ×1.5–4(–5) cm, cauline 5–18 × 1–2.5(–4) cm;

blade dull green, flat, oblanceolate to narrowly lanceolate or lanceolate to elliptic, margins bluntly dentate or subentire, teeth widely spaced or sinuate proximally;

bracts persistent.

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.

Inflorescences

erect, unbranched.

Flowers

opening near sunset;

buds erect, 5–8 mmdiam., with free tips terminal, erect, 1–3 mm;

floral tube 30–46 mm;

sepals yellowish green, also usually flushed with red or red-striped, 17–28 mm;

petals yellow, fading orange, pale yellow and somewhat opaque, very broadly obcordate, 13–23 mm, conspicuously shorter than sepals;

filaments 12–20 mm, anthers 7–12 mm, pollen ca. 50% fertile;

style 43–58 mm, stigma usually slightly exserted beyond anthers or surrounded by them 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

erect or slightly spreading, dark dull green and sometimes red-striped when dry, narrowly lanceoloid, 30–48 × 5–7 mm, free tips of valves 0.5–2.5mm.

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

0.9–2 × 0.9–1.3 mm.

asymmetrically cuneiform, 1.8–2.2(–2.6) mm.2n = 14.

2n

= 14.

Oenothera wolfii

Oenothera flava

Phenology Flowering Jun–Oct. Flowering Mar–Aug(–Oct).
Habitat Coarse-textured sandy or rocky sites, coastal dunes and bluffs, loose, sandy sites along roads, moist places. 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 0–100(–800) m. (0–300(–2600) ft.) 300–3200 m. (1000–10500 ft.)
Distribution
from FNA
CA; OR
[WildflowerSearch map]
[BONAP county map]
from FNA
AZ; CA; CO; ID; MT; ND; NE; NM; NV; OR; SD; UT; WA; WY; AB; MB; SK; Mexico (Chihuahua, Durango, Guanajuato, Hidalgo, Jalisco, Sonora)
[WildflowerSearch map]
[BONAP county map]
Discussion

Oenothera wolfii is a PTH species and forms a ring of 14 chromosomes in meiosis, and is self-compatible and autogamous (W. Dietrich et al. 1997). It has plastome I and a AA genome composition. It is known only from the vicinity of Port Orford, Curry County, Oregon (currently apparently only as far north as Otter Rock), south in a scattered distribution through Del Norte County to the mouth of the Mattole River, Humboldt County, California. The distribution, at least in California, is closely associated with small patches of Cenozoic-age marine sediments, isolated from each other by Franciscan sedimentary and metamorphic rocks. Most populations appear to occur near river mouths or to the south of a headland. The largest populations center in the area about 11 km long in the vicinity of Crescent City in Del Norte County, between Point George and Enderts Beach in Redwood National Park. There are collections from two inland California localities, one at the eastern border of Humboldt County, California (Willow Creek, Trinity River Valley), and the other at Carville, Trinity County, that may be O. wolfii. If so, they would presumably represent recent introductions and should be studied further. As summarized by Dietrich et al., O. wolfii is a rare endemic of coastal habitats and known from about 20 different sites. The total number of individuals of O. wolfii apparently fluctuates, with perhaps no more than about 5000 individuals total. It is threatened by any potential development and alteration of its habitat, presently by road maintenance and foot traffic. Another possibly more serious threat comes from the recent spread of O. glazioviana to this area. Oenothera glazioviana could swamp populations through hybridization and, perhaps, by direct competition.

Oenothera wolfii is in the Center for Plant Conservation’s National Collection of Endangered Plants.

(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 Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Oenothera > subsect. Oenothera Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Lavauxia > subsect. Lavauxia
Sibling taxa
O. acutissima, O. albicaulis, O. argillicola, O. arida, O. arizonica, O. biennis, O. boquillensis, O. brachycarpa, O. calcicola, O. californica, O. canescens, O. capillifolia, O. cavernae, O. cespitosa, O. cinerea, O. clelandii, O. coloradensis, O. cordata, O. coronopifolia, O. coryi, O. curtiflora, O. curtissii, O. deltoides, O. demareei, O. dodgeniana, O. drummondii, O. elata, O. engelmannii, O. falfurriae, O. filiformis, O. filipes, O. flava, O. fruticosa, O. gaura, O. gayleana, O. glaucifolia, O. glazioviana, O. grandiflora, O. grandis, O. harringtonii, O. hartwegii, O. havardii, O. heterophylla, O. hispida, O. howardii, O. humifusa, O. jamesii, O. kunthiana, O. laciniata, O. lavandulifolia, O. lindheimeri, O. linifolia, O. longissima, O. macrocarpa, O. mckelveyae, O. mexicana, O. nealleyi, O. neomexicana, O. nutans, O. nuttallii, O. oakesiana, O. organensis, O. pallida, O. parviflora, O. patriciae, O. perennis, O. pilosella, O. platanorum, O. podocarpa, O. primiveris, O. psammophila, O. pubescens, O. rhombipetala, O. riparia, O. rosea, O. serrulata, O. sessilis, O. simulans, O. sinuosa, O. spachiana, O. speciosa, O. stricta, O. suffrutescens, O. suffulta, O. tetraptera, O. texensis, O. toumeyi, O. triangulata, O. triloba, O. tubicula, O. villosa, O. xylocarpa
O. acutissima, O. albicaulis, O. argillicola, O. arida, O. arizonica, O. biennis, O. boquillensis, O. brachycarpa, O. calcicola, O. californica, O. canescens, O. capillifolia, O. cavernae, O. cespitosa, O. cinerea, O. clelandii, O. coloradensis, O. cordata, O. coronopifolia, O. coryi, O. curtiflora, O. curtissii, O. deltoides, O. demareei, O. dodgeniana, O. drummondii, O. elata, O. engelmannii, O. falfurriae, O. filiformis, O. filipes, O. fruticosa, O. gaura, O. gayleana, O. glaucifolia, O. glazioviana, O. grandiflora, O. grandis, O. harringtonii, O. hartwegii, O. havardii, O. heterophylla, O. hispida, O. howardii, O. humifusa, O. jamesii, O. kunthiana, O. laciniata, O. lavandulifolia, O. lindheimeri, O. linifolia, O. longissima, O. macrocarpa, O. mckelveyae, O. mexicana, O. nealleyi, O. neomexicana, O. nutans, O. nuttallii, O. oakesiana, O. organensis, O. pallida, O. parviflora, O. patriciae, O. perennis, O. pilosella, O. platanorum, O. podocarpa, O. primiveris, O. psammophila, O. pubescens, O. rhombipetala, O. riparia, O. rosea, O. serrulata, O. sessilis, O. simulans, O. sinuosa, O. spachiana, O. speciosa, O. stricta, O. suffrutescens, O. suffulta, O. tetraptera, O. texensis, O. toumeyi, O. triangulata, O. triloba, O. tubicula, O. villosa, O. wolfii, O. xylocarpa
Synonyms O. hookeri subsp. wolfii, Var. o. var. o. Lavauxiaflava a., L. palustris, L. taraxacoides, O. flava subsp. taraxacoides, O. murdockii, O. taraxacoides, O. triloba var. ecristata
Name authority (Munz) P. H. Raven, W. Dietrich & Stubbe: Syst. Bot. 4: 244. (1980) (A. Nelson) Garrett: Spring Fl. Wasatch ed. 4, 106. (1927)
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