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Wolf's evening-primrose

desert evening primrose, yellow desert 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 winter-annual, caulescent to short-caulescent, long-hirsute, hairs often with reddish purple pustulate bases, especially proximally, also moderately strigillose, and glandular puberulent distally, often on leaves; from a weakly fleshy 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) unbranched and erect or, sometimes, few branches from near base, in robust plants stems and caudex hollow and greatly enlarged, especially toward base, densely leafy, 5–35 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.

in a basal rosette, sometimes also cauline, (1.4–)6–15(–28) × (0.2–)1–3.5(–5.6) cm;

petiole (0.9–)3.5–8(–14) cm;

blade oblanceolate to linear-oblanceolate, pinnatifid or 2-pinnatifid to shallowly pinnately lobed, margins sinuate-dentate or subentire, apex obtuse.

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.

usually 1–4, rarely more, opening per day, 1–2 hours before sunset;

sepals (7–)12–25(–30) mm;

petals yellow, fading reddish orange to purple, obcordate to obovate, (6–)13–35(–40) mm;

filaments 6–16 mm, anthers 3–10 mm;

style (32–)40–90(–100) mm, stigma exserted beyond anthers or surrounded by them.

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.

woody in age, sigmoid or curved to nearly straight, lanceoloid to ovoid, 4-angled, 10–45(–60) × 4–8 mm, beak 4–15 mm, dehiscent 1/4–2/3 their length;

sessile.

Seeds

0.9–2 × 0.9–1.3 mm.

usually numerous, in 2 rows per locule, obovoid to oblanceoloid, 3–3.5 × 1–1.4 mm, surface thickened above raphe and at distal end into U-shaped structure.

2n

= 14.

= 14.

Oenothera wolfii

Oenothera primiveris

Phenology Flowering Jun–Oct. Flowering Feb–May(–Jun).
Habitat Coarse-textured sandy or rocky sites, coastal dunes and bluffs, loose, sandy sites along roads, moist places. Sandy soil on flats, low hills and margins of sand dunes, along arroyos, road­sides, in desert scrub, grasslands and oak-grasslands.
Elevation 0–100(–800) m. (0–300(–2600) ft.) 30–1600 m. (100–5200 ft.)
Distribution
from FNA
CA; OR
[WildflowerSearch map]
[BONAP county map]
from FNA
AZ; CA; NM; NV; TX; UT; Mexico (Baja California, Chihuahua, 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.)

Oenothera primiveris has a complex variation pattern (W. L. Wagner 2005). In the western part of the range from southeastern California across southern Nevada to southern Utah counties of Emery, Kane, and Washington, and northwestern Mohave County, Arizona, plants generally have a gray appearance, with dense pubescence and larger flowers with widespread self-compatibility, but with scattered populations retaining self-incompatibility. Populations from southof the Mogollon Plateau to southern New Mexico, western Texas, Chihuahua, Sonora, and Baja California, Mexico, are greener in appearance with smaller to much smaller flowers, and are all self-compatible with occasional outcrossing or complete autogamy. The transitions between these two extremes are so extensive and more or less gradual that it is not possible to subdivide into two subspecies as has been done previously (Wagner).

(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. Eremia
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. 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. 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. Lavauxia lobata, L. primiveris, O. bufonis, O. cespitosa var. primiveris, O. johnsonii, O. primiveris subsp. bufonis, O. primiveris var. bufonis, O. primiveris subsp. caulescens, O. primiveris var. caulescens, Pachylophus johnsonii
Name authority (Munz) P. H. Raven, W. Dietrich & Stubbe: Syst. Bot. 4: 244. (1980) A. Gray: Smithsonian Contr. Knowl. 5(6): 58. (1853)
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