The green links below add additional plants to the comparison table. Blue links lead to other Web sites.
enable glossary links

Wolf's evening-primrose

garden evening-primrose, large-flower evening primrose, red-sepal 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 biennial, densely to sparsely strigillose and villous, with spreading, red-pustulate hairs, also glandular puberulent and with only a few appressed hairs near inflorescence.
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.

erect, green or flushed with red on proximal parts, sometimes inflorescence axis red, usually withside branches obliquely arising from rosette and secondary branches from main stem, 50–150 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 and cauline, basal 13–30 × 3–5 cm, cauline 5–15 × 2.5–4 cm;

blade dark to bright green, white- or red-veined, narrowly oblanceolate to oblanceolate, sometimes narrowly elliptic to lanceolate distally, margins usually conspicuously crinkled, sometimes undulate, bluntly dentate, teeth widely spaced, sometimes sinuate-dentate proximally or lobed;

bracts persistent.

Inflorescences

erect, unbranched.

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.

opening near sunset;

buds erect, 7–9 mm diam., with free tips terminal, erect to spreading, 5–8 mm;

floral tube 35–50 mm;

sepals yellowish green, usually flushed with red or red-striped, sometimes very dark red throughout, 28–45 mm;

petals yellow to pale yellow, fading yellowish white and somewhat translucent, very broadly obcordate, 35–50 mm;

filaments 17–25 mm, anthers 10–12 mm, pollen ca. 50% fertile;

style 50–80 mm, stigma exserted beyond anthers at anthesis.

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.

erect or slightly spreading, dull green when dry, lanceoloid, 20–35 × 5–6 mm, free tips of valves 0.8–1.5 mm.

Seeds

0.9–2 × 0.9–1.3 mm.

1.3–2 ×1–1.5 mm, ca. 50% abortive.

2n

= 14.

= 14.

Oenothera wolfii

Oenothera glazioviana

Phenology Flowering Jun–Oct. Flowering (Jun–)Jul–Sep(–Oct).
Habitat Coarse-textured sandy or rocky sites, coastal dunes and bluffs, loose, sandy sites along roads, moist places. Open, disturbed sites.
Elevation 0–100(–800) m. (0–300(–2600) ft.) 20–600(–1400) m. (100–2000(–4600) ft.)
Distribution
from FNA
CA; OR
[WildflowerSearch map]
[BONAP county map]
from FNA
AL; AR; CA; CT; IL; IN; MA; ME; MI; MT; NC; NH; NJ; NY; OR; PA; RI; VT; WA; WI; WV; BC; MB; NS; ON; QC [Introduced in North America; introduced nearly worldwide in temperate and subtropical regions]
[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 glazioviana originated by hybridization between two cultivated or naturalized species in Europe and was introduced into the horticultural trade by Carter and Company of England in 1860 (R. E. Cleland 1972; P. H. Raven et al. 1979). The oldest name applied to this entity was based on plants cultivated in Rio de Janeiro in 1868; clearly, O. glazioviana must have spread very rapidly.

Oenothera glazioviana is a PTH species and forms a ring of 12 chromosomes and 1 bivalent in meiosis, and is self-compatible and autogamous (W. Dietrich et al. 1997). It has plastome II or III and a AB genome composition.

(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. Oenothera > subsect. Oenothera
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. 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. O. erythrosepala, O. grandiflora subsp. erythrosepala, Onagra erythrosepala
Name authority (Munz) P. H. Raven, W. Dietrich & Stubbe: Syst. Bot. 4: 244. (1980) Micheli in C. F. P. von Martius et al.: Fl. Brasil. 13(2): 178. (1875)
Web links