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Wolf's evening-primrose

large-flower 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, often appearing glabrous to naked eye, usually sparsely to moderately strigillose and villous with pustulate, translucent hairs proximal to inflorescence, pustules not red (in fresh material), inflorescence glabrous, glandular puberulent, or strigillose and glandular puberulent.
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, red on proximal parts, usually green on distal ones, rarely red throughout, unbranched or with branches obliquely arising from rosette and secondary branches arising from main stem, 100–300(–400) 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 18–32 × (2–)3–6.5 cm, cauline 6–20 × 1.5–6.5 cm;

blade soft and thin, bright green, usually flat, rarely undulate, narrowly oblanceolate to narrowly obovate, or narrowly elliptic to elliptic, sometimes narrowly ovate distally, margins bluntly dentate or subentire, teeth widely spaced, sometimes sinuate-dentate proximally or lobed;

bracts usually caducous.

Inflorescences

erect, unbranched.

erect, often with secondary or tertiary branches just proximal to main one.

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, 5–9 mm diam., with free tips terminal, erect, 2–9 mm;

floral tube 35–55 mm;

sepals yellowish green or flushed with red, 22–46 mm;

petals yellow to pale yellow, fading pale yellowish white, very broadly obcordate or obovate, (25–)30–45 mm;

filaments 18–27 mm, anthers 10–15 mm, pollen 90–100% fertile;

style 57–90 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, narrowly lanceoloid to narrowly ovoid, 15–35 × 3.5–5.5 mm, free tips of valves 0.5–2.5 mm.

Seeds

0.9–2 × 0.9–1.3 mm.

1–1.7 × 0.6–1.2 mm.

2n

= 14.

= 14.

Oenothera wolfii

Oenothera grandiflora

Phenology Flowering Jun–Oct. Flowering Jul–Aug(–Sep).
Habitat Coarse-textured sandy or rocky sites, coastal dunes and bluffs, loose, sandy sites along roads, moist places. Scattered, presumably relictual populations on chalky bluffs, loose sand over limestone, along streams, marshes, ditches, roadsides.
Elevation 0–100(–800) m. (0–300(–2600) ft.) 20–600 m. (100–2000 ft.)
Distribution
from FNA
CA; OR
[WildflowerSearch map]
[BONAP county map]
from FNA
AL; FL; MS; NC; SC; TN
[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 grandiflora has a scattered distribution, from the eastern half of Mississippi and Alabama, east to Tennessee (Franklin and Marion counties), North Carolina (Cherokee, Macon, Martin, Moore, New Hanover, Sampson, and Swain counties), South Carolina (Oconee, Spartanburg, and Sumter counties), and Florida (Alachua, Escambia, Franklin, Lake, Leon, Polk, Putnam, and Santa Rosa counties). Collections from southern Canada, New York, Pennsylvania, Vermont, and West Virginia almost certainly represent cultivated plants, garden escapes, or adventive populations, and the single locality from central Kentucky also may be an introduction; it is sometimes a colonizer in disturbed sites such as along roads.

Oenothera grandiflora has plastome III and a BB genome composition. As summarized by W. Dietrich et al. (1997), some populations of O. grandiflora seem to be entirely or mostly composed of self-incompatible individuals, whereas others consist of self-compatible plants. This is an extremely uncommon phenomenon within a single species of Oenothera; the only other species known to exhibit mixed populations of self-incompatible and self-compatible individuals is O. primiveris.

Oenothera grandiflora Lamarck 1798, being a later homonym of O. grandiflora L’Héritier 1789, pertains here.

(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. glazioviana, 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. biennis var. grandiflora, O. grandiflora var. glabra, O. grandiflora var. pubescens, O. lamarckiana, O. spectabilis
Name authority (Munz) P. H. Raven, W. Dietrich & Stubbe: Syst. Bot. 4: 244. (1980) L’Héritier in W. Aiton: Hort. Kew. 2: 2. (1789)
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