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

pink evening primrose, rose evening-primrose

Organ Mountain evening primrose

Habit Herbs perennial, caulescent, strigillose and often also sparsely hirsute; from slender taproot. Herbs perennial, moderately hirsute (hairs often with reddish purple, pustulate bases), alsostrigillose and becoming glandular puberulent distally; initially from slender taproot with single rosette, later developing numerous adventitious shoots from taproot and lateral roots, root system then appearing fibrous.
Stems

1–several, ascending to decumbent, 7–65 cm.

weakly erect to ascending, many from base, forming clumps 1–1.5 m diam., often branched distally, 30–60 cm.

Leaves

in a basal rosette and cauline, basal 1–6 × 0.3–2 cm, blade narrowly elliptic to elliptic or ovate, margins subentire, weakly serrulate, or sinuate-pinnatifid;

cauline 1–6 × 0.3–2 cm, blade narrowly elliptic to narrowly ovate, margins subentire or weakly serrulate, proximal ones sinuate-pinnatifid.

in a weakly developed basal rosette and cauline, basal 9–23 × 1–2.5 cm, cauline 5–11 × 1.5–3.5 cm;

petiole 0.5–1.5 cm;

blade very narrowly oblanceolate to narrowly elliptic, margins undulate, remotely and bluntly dentate.

Inflorescences

erect.

Flowers

1–3 opening per day near sunrise;

buds with free tips 0.1–1 mm;

floral tube 4–8 mm;

sepals 6–12 mm;

petals rose purple, fading darker, 4–12 mm;

filaments 4–6 mm, anthers 2–3.5 mm, pollen 35–65% fertile;

style 7–13.5 mm, stigma surrounded by anthers at anthesis.

opening near sunset, not strongly scented;

buds with free tips terminal, erect, 3–10 mm;

floral tube straight, 100–165(–190) mm;

sepals 25–50 mm;

petals yellow, fading deep reddish orange, broadly obovate with truncate apex, or obcordate, 30–55 mm;

filaments 18–35 mm, anthers 10–19 mm;

style 140–235 mm, stigma exserted beyond anthers at anthesis.

Capsules

narrowly obovoid, 4–12 × 2–4 mm, apex attenuate to a sterile beak, proximal stipe 5–20 mm, gradually tapering to base, valve midrib prominent in distal part;

sessile.

erect to slightly spreading at acute angle from stem, cylindrical, 25–35 ×4–5.5 mm, dehiscent at least 3/4 their length.

Seeds

narrowly obovoid, 0.5–0.9 × 0.3–0.5 mm.

numerous, in 2 distinct rows per locule, dark reddish brown, sometimes with darker flecks, obovoid, asymmetrical, irregularly angled, 1.5–2.1 × 1–1.2 mm, surface irregularly pitted and with collapsed papillae.

2n

= 14.

= 14.

Oenothera rosea

Oenothera organensis

Phenology Flowering Mar–Sep. Flowering Jun–Sep.
Habitat tropical areas.. In larger rhyolite canyons, along water courses, in eroded basins filled with gravel and rocks.
Elevation 10–600 m. (0–2000 ft.) 1800–2300 m. (5900–7500 ft.)
Distribution
from FNA
AZ; CA; TX; Mexico; Central America; West Indies; tropical areas [Introduced in South America (Argentina), Europe, Asia, s Africa, Atlantic Islands (Azores, Canary Islands)]
[WildflowerSearch map]
[BONAP county map]
from FNA
NM
[BONAP county map]
Discussion

Oenothera rosea is a PTH species, forming a ring of 14 chromosomes in meiosis, and is self-compatible and autogamous. In the flora area, it is known from Cochise, Pima, and Santa Cruz counties in Arizona, Alameda, Los Angeles, Riverside, San Bernardino, San Diego, San Francisco, and Santa Barbara counties in California (primarily in urban areas), and from southern Texas. It is clearly of North American origin, since all of its close relatives are confined to North America, and has spread south along the Andes. It occurs at 500–3700 m in South America but generally at lower elevations in most areas.

The name Hartmannia affinis Spach is illegitimate, being based on Oenothera virgata; H. gauroides Spach is also illegitimate, being based on O. rosea; O. purpurea Lamarck is a later homonym; these three names pertain here.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Oenothera organensis is known only from the Organ Mountains, Doña Ana County, especially on the east side. Various studies have been done to assess the status of this narrow endemic and estimate 2000 to 5000 individuals with wide fluctuations likely due to variation in rainfall (W. Dietrich et al. 1985). Oenothera organensis could decline if degradation of habitat increases in the Organ Mountains. The genetics and population biology of this taxon have been heavily studied in the past (summarized in Dietrich et al.). It is self-incompatible.

(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. Hartmannia Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Oenothera > subsect. Emersonia
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. 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
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. 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 Gaura epilobia, Godetia heuckii, Hartmannia rosea, H. rosea var. parvifolia, H. virgata, O. psycrophila, O. rosea var. parvifolia, O. rubra, O. virgata, Xylopleurum roseum O. macrosiphon
Name authority L’Héritier ex Aiton: Hort. Kew. 2: 3. (1789) Munz ex S. Emerson: Genetics 23: 190. (1938)
Web links