Oenothera organensis |
Oenothera triloba |
|
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Organ Mountain evening primrose |
stemless evening-primrose |
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Habit | 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. | Herbs winter-annual, sometimes biennial, acaulescent or very short-caulescent, sparsely to moderately strigillose and glandular puberulent, sometimes one hair type predominant, rarely glabrate, sometimes also very sparsely hirsute, especially on leaf veins; from a slender or, sometimes, stout taproot. |
Stems | weakly erect to ascending, many from base, forming clumps 1–1.5 m diam., often branched distally, 30–60 cm. |
(when present) ascending, 1–several, densely leafy, 0–20 cm. |
Leaves | 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. |
in a basal rosette, sometimes also cauline, (2.5–)6–25(–32) × (0.6–)1.5–4(–5) cm, thin; petiole (0.5–)1–8 cm; blade oblanceolate to elliptic, margins irregularly pinnatifid, sometimes subentire, apex acute to obtuse or rounded. |
Flowers | 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. |
1–4 opening per day near sunset, without noticeable scent; buds with subequal free tips 2–7 mm; floral tube (20–)28–95(–138) mm; sepals (6–)10–30(–35) mm; petals pale yellow, fading pale orange, drying lavender, (10–)12–30(–38) mm; filaments (5–)8–15(–18) mm, anthers (3.5–)4–11 mm; style (3.4–)4.2–11.5(–16.3) mm, stigma usually surrounded by anthers, sometimes (especially in some Texas populations) exserted beyond anthers. |
Capsules | erect to slightly spreading at acute angle from stem, cylindrical, 25–35 ×4–5.5 mm, dehiscent at least 3/4 their length. |
woody in age, rhombic-obovoid, winged, wings broadly triangular, 5–10 mm wide, often terminating in a hooked tooth, (10–)15–25(–28) × 4–8 mm (excluding wings), valve surface reticulate, dehiscent 1/8–1/3 their length. |
Seeds | 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. |
asymmetrically cuneiform, (2.1–)2.5–3(–3.3) mm. |
2n | = 14. |
= 14. |
Oenothera organensis |
Oenothera triloba |
|
Phenology | Flowering Jun–Sep. | Flowering (Feb–)Mar–May(–Jul). |
Habitat | In larger rhyolite canyons, along water courses, in eroded basins filled with gravel and rocks. | Scattered to common in clay, sandy or rocky soil, playas, floodplains, creek beds, slopes and flats, moist sites, disturbed sites, roadsides, old fields, in Larrea deserts, prairies, glades. |
Elevation | 1800–2300 m. (5900–7500 ft.) | 300–1900 m. (1000–6200 ft.) |
Distribution |
NM |
AL; AR; CO; DC; IL; IN; KS; KY; MD; MO; NM; OH; OK; PA; TN; TX; VA; Mexico (Baja California, Chihuahua, Nuevo León)
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Discussion | 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.) |
Oenotheratriloba is primarily a species of the high plains from eastern Socorro County, New Mexico, east through all but eastern Texas, Oklahoma, to southern Kansas, east of Meade and Pawnee counties and south of Douglas and Saline counties. It becomes more sporadic eastward into Missouri south of the Missouri River, northwestern and north-central Arkansas, central and eastern Tennessee, northern Alabama, and Logan and Warren counties, Kentucky; also known from disjunct sites in northern Mexico from Nuevo León, Chihuahua, and Baja California, Mexico; and, introduced in Illinois, Indiana, Ohio, Kentucky (Campbell and Fayette counties), Pennsylvania, Virginia, Maryland, and the District of Columbia. Areas where it was introduced are represented by old collections; no current information indicates their continued presence in any of these areas. It was recently collected in Baca County, Colorado. Capsules of dead plants sometimes form pineconelike clusters of ten to 100 or more capsules. The illegitimate names Lavauxia nuttalliana Spach and L. triloba (Nuttall) Spach var. watsonii Britton pertain here. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 10. | FNA vol. 10. |
Parent taxa | ||
Sibling taxa | ||
Synonyms | O. macrosiphon | Lavauxiahamata wooton, L. triloba, L. watsonii, O. hamata, O. rhizocarpa, O. roemeriana, O. triloba var. parviflora, O. triloba |
Name authority | Munz ex S. Emerson: Genetics 23: 190. (1938) | Nuttall: J. Acad. Nat. Sci. Philadelphia 2: 118. (1821) |
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