Oenothera laciniata
Oenothera serrulata
cut-leaf evening-primrose, southern evening primrose
serrate-leaf evening primrose, yellow evening-primrose, yellow sundrops
erect to ascending, unbranched to much branched, 5–50 cm.
1–many, weakly decumbent to erect, unbranched to moderately branched, 10–60(–80) cm.
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.
1–9 × 0.1–1 cm, sometimes fascicles of small leaves to 2 cm present in non-flowering axils;
petiole 0–0.6 cm;
blade linear to narrowly lanceolate or oblanceolate, often folded lengthwise, usually not much reduced distally, proximalmost stem leaves often narrowly oblanceolate to oblanceolate, sometimes spatulate, base attenuate, margins subentire or spinulose-serrate, apex acute.
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 sunrise;
buds with free tips 0–4 mm;
floral tube 2–12(–16) mm;
sepals 1.5–9 mm, midribs keeled;
petals yellow, fading dark yellow to orange, 5–12(–20) mm; antisepalous filaments 1–5(–7) mm, antipetalous filaments 0.5–3 mm, anthers 1.5–4(–6) mm, pollen 30–60(–80)% fertile;
style 2–15(–20) mm, stigma discoid to quadrangular, surrounded by anthers at anthesis.
cylindrical, sometimes slightly enlarged toward apex, 20–50 × 2–4 mm.
6–25 × 1–3 mm, hard, dehiscent 1/2 their length, often tardily dehiscent through their length.
ellipsoid to subglobose, 0.9–1.8 × 0.4–0.9 mm.
obovoid, 1–1.8 mm, sharply angled, apex truncate.
= 14.
= 14.
Oenothera laciniata
Oenothera serrulata
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 serrulata occurs from southern Alberta, southern Saskatchewan, and southern Manitoba to eastern New Mexico, the Texas Panhandle, and the Gulf Coast of Texas, including eastern Montana, eastern Wyoming, eastern Colorado, North Dakota, South Dakota, Nebraska, Kansas, western and central Oklahoma, western and southern Minnesota, Iowa, northwestern Missouri, and with outlying populations in central Illinois, northern Indiana, southeastern Wisconsin, northwestern peninsular Michigan, east-central Arizona, and west-central Chihuahua, Mexico; it is naturalized in Ontario. It was documented in 1909 as a non-native in Vermont and has not been collected since. Oenothera serrulata is a PTH species and forms a ring of 12 + 1II or a ring of 14 chromosomes in meiosis, and is self-compatible and autogamous (H. F. Towner 1977).
Calylophus nuttallii Spach is a superfluous name that pertains here. Oenothera spachiana Steudel August 1840 (not Torrey & A. Gray June 1840) is an illegitimate later homonym and also pertains here.
H. F. Towner (1977) is followed here in recognition of a broadly delimited Oenothera serrulata as a complex assemblage of populations that are all primarily autogamous and are PTH. These populations consist of wide morphological diversity involving leaf size and shape, stature, pubescence, and flower size. Some of these variants may have evolved independently from O. capillifolia. Flower size is variable throughout the geographical range, and some of the largest flowered forms occur near large-flowered populations of O. capillifolia subsp. capillifolia in central Oklahoma. Most populations occurring west of approximately 98°W longitude comprise well-branched, short-leaved, and relatively low-statured plants, while those east of that line are less branched, taller and more erect, long-leaved, and densely strigillose. Populations along the Texas Gulf Coast described as Calylophus australis are rather distinctive and are separated from the remainder of the populations of O. serrulata primarily in less dense pubescence, shorter, coarsely serrate leaves, and more erect stems. They may have been independently derived from O. capillifolia. In his revision, Towner did not continue to recognize them because there were no data available on the phylogeny of other populations of O. serrulata. Subsequent detailed analyses (B. Cooper, unpubl.) indicate that the Texas coastal populations described as C. australis arose independently from other populations of O. serrulata, but O. serrulata also has multiple apparent origins from O. capillifolia.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
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