Oenothera biennis
Onagraceae tribe Onagreae
common evening-primrose, eastern evening primrose, evening star, King's-cureall, small flower evening primrose
erect, green or flushed with red on proximal parts, sometimes inflorescence axis red, unbranched or with side branches obliquely arising from rosette or stem, 30–200 cm.
in a basal rosette and cauline, basal 10–30 × 2–5 cm, cauline 5–22 ×(1–)1.5–5(–6) cm;
blade usually green to pale green, narrowly oblanceolate to oblanceolate, sometimes narrowly elliptic to elliptic distally, margins usually flat, rarely undulate, bluntly dentate, teeth widely spaced, sometimes sinuate-dentate proximally or lobed;
bracts persistent.
alternate or basal;
stipules absent.
erect, unbranched or with secondary branches just proximal to main one, internodes in fruit usually shorter than capsule.
opening near sunset;
buds erect, 3.5–6 mm diam., with free tips terminal, erect or spreading, 1.5–3 mm;
floral tube (20–)25–40 mm;
sepals yellowish green, rarely flushed with red or red-striped, 12–22(–28) mm;
petals yellow to pale yellow, fading yellowish white and somewhat translucent, very broadly obcordate, 12–25(–30) mm;
filaments 8–15(–20) mm, anthers 3–6(–9) mm, pollen 50% fertile;
style 30–55 mm, stigma surrounded by anthers at anthesis.
usually actinomorphic, rarely slightly zygomorphic (in Oenothera), (3 or)4-merous;
stamens 2 times as many, or rarely as many, as sepals;
pollen usually shed in monads, rarely tetrads (Chylismia sect. Lignothera).
a dry capsule, usually dehiscent, sometimes indehiscent.
erect or slightly spreading, dull green when dry, lanceoloid, 20–40 × 4–6 mm, free tips of valves 0.8–1.5 mm.
1–1.2 × 0.6–1.1 mm.
few to numerous, without hairs or wings, [very rarely with asymmetrical dry wing (Xylonagra)], or with dry (Oenothera), erose or smooth wing, or with thick, papillate wings (Chylismiella).
= 14.
Oenothera biennis
Onagraceae tribe Onagreae
Oenothera biennis is a PTH species and usually forms a ring of 14 chromosomes or a ring of 12 and 1 bivalent in meiosis, and is self-compatible and autogamous (W. Dietrich et al. 1997). It has plastome II and a BA or AB genome composition across different populations.
W. Dietrich et al. (1997) found that in the western half of the United States, where Oenothera biennis is most likely introduced, there are distinctive series of forms that seemed similar to a phenotype of O. biennis that originated in Europe. The most distinctive morphological characters of this western form are the densely villous stems with pustulate hairs and the intense, often dark red color of the stems and sepals, characters which are not typical for the eastern North America forms of O. biennis. The pustulate pubescence of this form is also a characteristic feature of many O. elata and O. villosa subsp. strigosa forms, suggesting possible past hybridization with them. Crossing studies confirm that one of these taxa was most likely involved, and these studies showed that, like O. biennis, they are all AB and BA genomic combinations. One of the seemingly odd features of this form is its scattered distribution across a wide expanse of western states. A possible explanation is that perhaps O. biennis spread westward during glacial periods, hybridized with AA taxa (O. elata and O. villosa subsp. strigosa), followed by compression during warming periods since. A hypothesis of repeated recent hybridization does not seem likely since more typical eastern forms of O. biennis are not present throughout much of the western states. Oenothera biennis hybridizes with the other species of subsect. Oenothera with which it comes in contact, includingO. grandiflora, O. nutans, O. oakesiana, O. parviflora, O. villosa subsp. strigosa, and O. villosa subsp. villosa.
Oenothera biennis subsp. rubricaulis (Klebahn) Stomps is a later homonym that pertains here.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
Genera 13, species 265 (12 genera, 199 species in the flora).
Onagreae account for more than half the total genera in Onagraceae and diversified from a center in southwestern North America (L. Katinas et al. 2004). Delimitation of the tribe by W. L. Wagner et al. (2007) differs from previous ones by the exclusion of Gongylocarpus, now in its own tribe, by the segregation of eight genera (Camissoniopsis, Chylismia, Chylismiella, Eremothera, Eulobus, Neoholmgrenia, Taraxia, and Tetrapteron) from Camissonia, and by the inclusion of three previously separate genera (Calylophus, Gaura, and Stenosiphon) in Oenothera. Within the branch of the family that lacks stipules (Gongylocarpeae, Epilobieae, and Onagreae), the last two tribes form a clade that has very strong molecular support (R. A. Levin et al. 2003, 2004), but no obvious morphological synapomorphy. The clade may be defined by a cytogenetic change from the base chromosome number of x = 11 found in Circaeeae, Gongylocarpeae, and Lopezieae, to x = 18 in Epilobieae, and x = 7 in Onagreae; however, these changes could also have occurred independently. Other than the new chromosome number x = 7, the only apparent morphological synapomorphy for Onagreae alone is pollen with prominent apertural protrusions (J. Praglowski et al. 1987, 1989), a character state also found in Circaeeae (Praglowski et al. 1994). The monophyly of Onagreae has moderate (Levin et al. 2004) to strong support (V. S. Ford and L. D. Gottlieb 2007).
(Discussion copyrighted by Flora of North America; reprinted with permission.)
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