Oenothera macrocarpa |
Oenothera glazioviana |
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bigfruit evening primrose, Missouri evening primrose, Ozark sundrop |
garden evening-primrose, large-flower evening primrose, red-sepal evening-primrose |
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Habit | Herbs caulescent, strigillose or glabrous, sometimes glandular puberulent distally; from a stout taproot, sometimes lateral roots producing adventitious shoots. | Herbs biennial, densely to sparsely strigillose and villous, with spreading, red-pustulate hairs, also glandular puberulent and with only a few appressed hairs near inflorescence. | ||||||||||||||||
Stems | moderately leafy, (1–)4–40(–60) cm. |
erect, green or flushed with red on proximal parts, sometimes inflorescence axis red, usually withside branches obliquely arising from rosette and secondary branches from main stem, 50–150 cm. |
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Leaves | cauline, (2.8–)3.7–12.5(–17) × (0.1–)0.4–3(–4.5) cm; petiole (0.4–)1–4(–6) cm; blade linear, lanceolate-elliptic, elliptic to oblanceolate or suborbiculate, margins entire or conspicuously or inconspicuously denticulate or serrulate, sometimes undulate, apex usually acute, sometimes obtuse or retuse (subsp. incana). |
in a basal rosette and cauline, basal 13–30 × 3–5 cm, cauline 5–15 × 2.5–4 cm; blade dark to bright green, white- or red-veined, narrowly oblanceolate to oblanceolate, sometimes narrowly elliptic to lanceolate distally, margins usually conspicuously crinkled, sometimes undulate, bluntly dentate, teeth widely spaced, sometimes sinuate-dentate proximally or lobed; bracts persistent. |
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Inflorescences | erect, unbranched. |
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Flowers | usually 1 or 2, rarely more, opening per day near sunset, fading next morning, sometimes (subspp. |
opening near sunset; buds erect, 7–9 mm diam., with free tips terminal, erect to spreading, 5–8 mm; floral tube 35–50 mm; sepals yellowish green, usually flushed with red or red-striped, sometimes very dark red throughout, 28–45 mm; petals yellow to pale yellow, fading yellowish white and somewhat translucent, very broadly obcordate, 35–50 mm; filaments 17–25 mm, anthers 10–12 mm, pollen ca. 50% fertile; style 50–80 mm, stigma exserted beyond anthers at anthesis. |
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Capsules | papery in age, narrowly ellipsoid to lanceoloid, sometimes twisted (subsp. fremontii), winged, wings (2–)10–28(–34) mm wide, body (13–)25–70(–115) × 2–9 mm, dehiscent 1/4–1/3 their length; pedicel 1–12(–25) mm. |
erect or slightly spreading, dull green when dry, lanceoloid, 20–35 × 5–6 mm, free tips of valves 0.8–1.5 mm. |
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Seeds | numerous, rarely as few as 8, in 1 row per locule, obovoid, (2–)3–5 × 1–2.3 mm. |
1.3–2 ×1–1.5 mm, ca. 50% abortive. |
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Macrocarpa | and oklahomensis) lasting for 2 days, weakly scented; buds with unequal free tips 1–11(–15) mm; floral tube (21–)35–140(–160) mm; sepals (20–)25–65(–75) mm; petals bright yellow, fading orange, reddish orange or mostly unchanged, obovate to very broadly obovate, (17–)25–65(–68) mm, usually with terminal notch and/or tooth, margin sometimes erose; filaments 13–40(–44) mm, anthers 10–24(–25) mm; style (45–)55–192 mm, stigma usually exserted beyond anthers at anthesis. |
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2n | = 14. |
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Oenothera macrocarpa |
Oenothera glazioviana |
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Phenology | Flowering (Jun–)Jul–Sep(–Oct). | |||||||||||||||||
Habitat | Open, disturbed sites. | |||||||||||||||||
Elevation | 20–600(–1400) m. (100–2000(–4600) ft.) | |||||||||||||||||
Distribution |
c United States; n Mexico; s United States
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AL; AR; CA; CT; IL; IN; MA; ME; MI; MT; NC; NH; NJ; NY; OR; PA; RI; VT; WA; WI; WV; BC; MB; NS; ON; QC [Introduced in North America; introduced nearly worldwide in temperate and subtropical regions]
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Discussion | Subspecies 5 (4 in the flora). Oenotheramacrocarpa is variable and has differentiated extensively in the Great Plains region. Each of the five distinctive subspecies occupies a different geographical and ecological situation. Only subsp. mexicana W. L. Wagner from Coahuila, Mexico, occurs outside of the flora area. In general, the subspecies are sharply distinct and each is characterized by a number of features, including pubescence, leaf features, flower and floral tube size, and size and morphology of the capsules and seeds. The five entities are treated as subspecies primarily because of their complete interfertility and extensive intergradation in any area of marginal contact. Intermediates are known between subsp. macrocarpa and subspp. fremontii and oklahomensis and between subspp. incana and oklahomensis. There is also some evidence that suggests past hybridization between subspp. fremontii and incana although there is no present contact between them. All subspecies are self-incompatible. Oenothera alata Nuttall (1818) is an illegitimate name based on O. macrocarpa and pertains here. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Oenothera glazioviana originated by hybridization between two cultivated or naturalized species in Europe and was introduced into the horticultural trade by Carter and Company of England in 1860 (R. E. Cleland 1972; P. H. Raven et al. 1979). The oldest name applied to this entity was based on plants cultivated in Rio de Janeiro in 1868; clearly, O. glazioviana must have spread very rapidly. Oenothera glazioviana is a PTH species and forms a ring of 12 chromosomes and 1 bivalent in meiosis, and is self-compatible and autogamous (W. Dietrich et al. 1997). It has plastome II or III and a AB genome composition. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 10. | FNA vol. 10. | ||||||||||||||||
Parent taxa | Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Megapterium | Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Oenothera > subsect. Oenothera | ||||||||||||||||
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Subordinate taxa | ||||||||||||||||||
Synonyms | Megapterium macrocarpum, M. nuttallianum | O. erythrosepala, O. grandiflora subsp. erythrosepala, Onagra erythrosepala | ||||||||||||||||
Name authority | Nuttall: Cat. Pl. Upper Louisiana, no. 56. (1813) | Micheli in C. F. P. von Martius et al.: Fl. Brasil. 13(2): 178. (1875) | ||||||||||||||||
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