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Chilean evening primrose
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Organ Mountain evening primrose
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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. |
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weakly erect to ascending, many from base, forming clumps 1–1.5 m diam., often branched distally, 30–60 cm. |
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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. |
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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. |
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erect to slightly spreading at acute angle from stem, cylindrical, 25–35 ×4–5.5 mm, dehiscent at least 3/4 their length. |
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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. |
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= 14. |
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Flowering Jun–Sep. |
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In larger rhyolite canyons, along water courses, in eroded basins filled with gravel and rocks. |
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1800–2300 m. (5900–7500 ft.) |
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South America [Introduced, California] |
NM |
Subspecies 2 (1 in the flora). Oenothera stricta is a PTH species and forms a ring of 14 chromosomes in meiosis, and is self-compatible and autogamous (W. Dietrich 1977). Subspecies stricta is naturalized in many areas around the world and may be so in California. Subspecies altissima W. Dietrich occurs only in Argentina. (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.) |
| FNA vol. 10. |
FNA vol. 10. |
| Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Oenothera > subsect. Munzia > ser. Allochroa |
Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Oenothera > subsect. Emersonia |
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. 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 |
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O. macrosiphon |
| Ledebour ex Link: Enum. Hort. Berol. Alt. 1: 377. (1821) — (as striata) |
Munz ex S. Emerson: Genetics 23: 190. (1938) |
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