Oenothera wolfii
Oenothera serrulata
Wolf's evening-primrose
serrate-leaf evening primrose, yellow evening-primrose, yellow sundrops
erect, green, flushed with red proximally or red throughout, unbranched or branches obliquely arising from rosette and sometimes secondary branches arising from main stem, 50–100 cm.
1–many, weakly decumbent to erect, unbranched to moderately branched, 10–60(–80) cm.
in a basal rosette and cauline, basal 13–35 ×1.5–4(–5) cm, cauline 5–18 × 1–2.5(–4) cm;
blade dull green, flat, oblanceolate to narrowly lanceolate or lanceolate to elliptic, margins bluntly dentate or subentire, teeth widely spaced or sinuate proximally;
bracts persistent.
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.
erect, unbranched.
opening near sunset;
buds erect, 5–8 mmdiam., with free tips terminal, erect, 1–3 mm;
floral tube 30–46 mm;
sepals yellowish green, also usually flushed with red or red-striped, 17–28 mm;
petals yellow, fading orange, pale yellow and somewhat opaque, very broadly obcordate, 13–23 mm, conspicuously shorter than sepals;
filaments 12–20 mm, anthers 7–12 mm, pollen ca. 50% fertile;
style 43–58 mm, stigma usually slightly exserted beyond anthers or surrounded by them 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.
erect or slightly spreading, dark dull green and sometimes red-striped when dry, narrowly lanceoloid, 30–48 × 5–7 mm, free tips of valves 0.5–2.5mm.
6–25 × 1–3 mm, hard, dehiscent 1/2 their length, often tardily dehiscent through their length.
0.9–2 × 0.9–1.3 mm.
obovoid, 1–1.8 mm, sharply angled, apex truncate.
= 14.
= 14.
Oenothera wolfii
Oenothera serrulata
Oenothera wolfii is a PTH species and forms a ring of 14 chromosomes in meiosis, and is self-compatible and autogamous (W. Dietrich et al. 1997). It has plastome I and a AA genome composition. It is known only from the vicinity of Port Orford, Curry County, Oregon (currently apparently only as far north as Otter Rock), south in a scattered distribution through Del Norte County to the mouth of the Mattole River, Humboldt County, California. The distribution, at least in California, is closely associated with small patches of Cenozoic-age marine sediments, isolated from each other by Franciscan sedimentary and metamorphic rocks. Most populations appear to occur near river mouths or to the south of a headland. The largest populations center in the area about 11 km long in the vicinity of Crescent City in Del Norte County, between Point George and Enderts Beach in Redwood National Park. There are collections from two inland California localities, one at the eastern border of Humboldt County, California (Willow Creek, Trinity River Valley), and the other at Carville, Trinity County, that may be O. wolfii. If so, they would presumably represent recent introductions and should be studied further. As summarized by Dietrich et al., O. wolfii is a rare endemic of coastal habitats and known from about 20 different sites. The total number of individuals of O. wolfii apparently fluctuates, with perhaps no more than about 5000 individuals total. It is threatened by any potential development and alteration of its habitat, presently by road maintenance and foot traffic. Another possibly more serious threat comes from the recent spread of O. glazioviana to this area. Oenothera glazioviana could swamp populations through hybridization and, perhaps, by direct competition.
Oenothera wolfii is in the Center for Plant Conservation’s National Collection of Endangered Plants.
(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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