Oenothera howardii
Oenothera biennis
Howard's evening-primrose
common evening-primrose, eastern evening primrose, evening star, King's-cureall, small flower evening primrose
(when present) ascending, longer ones becoming decumbent, leafy, sometimes densely so, 0–10(–30) cm.
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, sometimes also cauline, (6–)8.5–17(–23) × (0.5–)1–2(–3) cm;
petiole 2–7.5 cm;
blade usually oblanceolate, elliptic to narrowly oblong, rarely lanceolate, margins often undulate, entire or remotely and irregularly pinnately lobed mostly in proximal 1/2, rarely more regularly pinnately lobed and lobing extending to distal 1/2, sinuses usually extending less than 1/2 to midrib, lobes triangular to oblong or linear, (1–)4–9(–13) mm, apex acute to obtuse.
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.
erect, unbranched or with secondary branches just proximal to main one, internodes in fruit usually shorter than capsule.
usually 1 or 2, rarely more, opening per day near sunset, strongly and sweetly scented;
buds with unequal free tips 1–3(–4) mm;
floral tube (43–)60–110(–125) mm;
sepals (30–)35–60(–80) mm;
petals brilliant yellow, fading deep red, drying deep reddish purple to reddish brown, usually broadly obovate, rarely subrhombic, (30–)40–60(–73) mm, sometimes with a terminal tooth;
filaments (19–)25–38 mm, anthers 10–17 mm;
style(90–)110–145(–165) mm, stigma exserted beyond anthers at anthesis.
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.
leathery, ovoid, narrowly ovoid, or narrowly lanceoloid to broadly ellipsoid, winged, wings (2–)4–7(–11) mm wide, body (20–)25–50(–80) × 4–6 mm, dehiscent 1/4–1/3 their length;
pedicel 2–6 mm.
erect or slightly spreading, dull green when dry, lanceoloid, 20–40 × 4–6 mm, free tips of valves 0.8–1.5 mm.
numerous, usually in 1 row per locule, rarely in 2 rows toward base, obovoid to subcuboid, 3–8 × 2.5–3.5 mm.
1–1.2 × 0.6–1.1 mm.
= 28, 42, 56.
= 14.
Oenothera howardii
Oenothera biennis
Oenotherahowardii is known from three disjunct areas: three collections on the High Plains (Baca and Otero counties, Colorado, and Hamilton County, Kansas); open yucca-juniper grassland, rocky slopes or disturbed areas on shale substrates along the Colorado counties of Boulder, Denver, Jefferson, and Larimer, and just over the state line in Wyoming; and, common to scattered, mostly on rocky slopes but also in shaded canyon sites on fine-textured red sandstones, clays, gypsum, chalky white degraded limestone or limestone in pinyon-juniper woodland to ponderosa pine-Douglas fir forest in southern Utah and eastern Nevada.
A. Nelson intended to publish Lavauxia howardii as a new combination and base it on Oenothera howardii M. E. Jones (1893), which was not validly published at the time, but inadvertently published L. howardii as a new species. Oenothera howardii (A. Nelson) W. L. Wagner is an isonym.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
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.)
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