Oenothera laciniata |
Oenothera organensis |
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cut-leaf evening-primrose, southern evening primrose |
Organ Mountain evening primrose |
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Habit | Herbs annual, sparsely to moderately strigillose, sometimes also villous, sometimes also becoming glandular puberulent distally. | 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 | erect to ascending, unbranched to much branched, 5–50 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 4–15 × 1–3 cm, cauline 2–10 × 0.5–3.5 cm; blade green, narrowly oblanceolate to narrowly elliptic or narrowly oblong, margins usually dentate or deeply lobed; bracts spreading, flat. |
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. |
Flowers | usually 1 opening per day near sunset; buds erect, with free tips erect, 0.3–3 mm; floral tube 12–35 mm; sepals 5–15 mm; petals yellow, fading orange or reddish tinged, broadly obovate or obcordate, 5–22 mm; filaments 3–14 mm, anthers 4–5 mm, pollen ca. 50% fertile; style 20–50 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 | cylindrical, sometimes slightly enlarged toward apex, 20–50 × 2–4 mm. |
erect to slightly spreading at acute angle from stem, cylindrical, 25–35 ×4–5.5 mm, dehiscent at least 3/4 their length. |
Seeds | ellipsoid to subglobose, 0.9–1.8 × 0.4–0.9 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 laciniata |
Oenothera organensis |
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Phenology | Flowering (Feb–)Apr–Sep(–Oct). | Flowering Jun–Sep. |
Habitat | introduced nearly worldwide in temperate and subtropical areas.. | In larger rhyolite canyons, along water courses, in eroded basins filled with gravel and rocks. |
Elevation | 0–1000(–1300) m. (0–3300(–4300) ft.) | 1800–2300 m. (5900–7500 ft.) |
Distribution |
AL; AR; CA; CT; DC; DE; FL; GA; IA; IL; IN; KS; KY; LA; MA; MD; ME; MI; MN; MO; MS; NC; ND; NE; NJ; NM; NY; OH; OK; PA; RI; SC; SD; TN; TX; VA; VT; WI; WV; WY [Introduced nearly worldwide in temperate and subtropical areas]
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NM |
Discussion | Oenothera laciniata is a PTH species and forms aring of 14 chromosomes in meiosis, and is self-compatible and autogamous (W. Dietrich and W. L. Wagner 1988). Oenothera laciniata is known in New Mexico from Doña Ana and Roosevelt counties from non-montane habitats and thus do not appear to represent O. pubescens; however, a few collections from Brewster and Jeff Davis counties, Texas, reported by W. Dietrich and W. L. Wagner (1988) as O. laciniata appear to represent collections of O. pubescens. Dietrich and Wagner found that O. laciniata hybridizes not only with O. grandis, but also with O. drummondii subsp. drummondii, O. humifusa, and O. mexicana. It is naturalized nearly worldwide in temperate and subtropical areas. (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. Oenothera > subsect. Raimannia | Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Oenothera > subsect. Emersonia |
Sibling taxa | ||
Synonyms | O. minima, O. repanda, O. sinuata, O. sinuata var. minima, Onagra sinuata, Raimannia laciniata | O. macrosiphon |
Name authority | Hill: Veg. Syst. 12(app.): 64, plate 10. (1767) | Munz ex S. Emerson: Genetics 23: 190. (1938) |
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