Oenothera filiformis |
Oenothera jamesii |
|
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bee-blossom, longflower beeblossom |
trumpet evening primrose |
|
Habit | Herbs usually robust winter-annual, sometimes biennial, moderately to densely strigillose, sometimes also glandular puberulent, villous and/or short-hirtellous; from fleshy taproot. | Herbs biennial or winter-annual, usually predominately and densely strigillose, sometimes also villous with scattered, appressed hairs, rarely with a few pustulate hairs, inflorescence sometimes also glandular puberulent. |
Stems | usually well-branched distal to base, (50–)100–400 cm. |
erect, usually green, rarely flushed with red, unbranched or with branches arising obliquely from rosette and secondary branches arising from main stem, 60–180 cm. |
Leaves | in a basal rosette and cauline, basal 8–15(–40) × 1.5–3.6 cm, blade lyrate, margins irregularly toothed to lobed; cauline 1.5–13 × 0.5–3 cm, blade narrowly elliptic to elliptic or lanceolate, margins subentire or shallowly undulate-denticulate. |
in a basal rosette and cauline, basal 10–30 × 2.5–5 cm, cauline 4–20 × 1–5 cm; blade dull green, flat, narrowly oblanceolate, oblanceolate to narrowly elliptic, or narrowly lanceolate, margins bluntly dentate or subentire, teeth widely spaced; bracts persistent. |
Inflorescences | erect, usually unbranched, rarely with few lateral branches. |
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Flowers | 4-merous, zygomorphic, opening at sunset; floral tube 4–13(–15) mm; sepals 7–18 mm; petals white, fading pink, elliptic to elliptic-obovate, 7–15 mm; filaments 5–13 mm, anthers 1.5–5 mm, pollen 90–100% fertile; style 12–34 mm, stigma exserted beyond anthers at anthesis. |
opening near sunset; buds erect, 7–12 mm diam., with free tips terminal, erect, 0.5–3 mm; floral tube persistent on ovary after anthesis, (60–)80–120(–160) mm; sepals yellowish green, red-striped to red throughout, 30–55 mm; petals yellow, fading orange or pale yellow, very broadly obcordate, 40–50 mm; filaments 23–30 mm, anthers 12–22 mm, pollen 90–100% fertile; style 90–170(–200) mm, stigma exserted beyond anthers at anthesis. |
Capsules | ellipsoid or ovoid, sharply 4-angled, 4.5–7 × 1.5–2.5 mm; sessile. |
erect or slightly spreading, dull green or gray-green when dry, narrowly lanceoloid, 20–50 × 6–12 mm, free tips of valves 2.5–5 mm. |
Seeds | 2–4, yellowish to reddish brown, 1.3–3 × 0.7–1.3 mm. |
1–1.2 × 0.7–1.3 mm. |
2n | = 14. |
= 14. |
Oenothera filiformis |
Oenothera jamesii |
|
Phenology | Flowering (Jun–)Jul–Oct(–Nov). | Flowering Jul–Sep(–Oct). |
Habitat | Open woods, fields, along streams, sandy soil, disturbed sites, ditch banks, roadsides, railway embankments. | Sandy stream banks, ditches, moist areas, cultivated areas, disturbed roadsides. |
Elevation | 10–500 m. (0–1600 ft.) | (30–)300–1800 m. ((100–)1000–5900 ft.) |
Distribution |
AL; AR; CO; CT; IA; IL; IN; KS; KY; LA; MA; MD; MI; MO; MS; NE; OH; OK; PA; TN; TX; WI; ON
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KS; OK; TX; Mexico (Coahuila, Nuevo León, Puebla) [Introduced in e Asia (Japan), s Africa, Atlantic Islands (Canary Islands)] |
Discussion | P. H. Raven and D. P. Gregory (1972[1973]) found various levels of hybridization and intergradation between Oenothera filiformis and O. lindheimeri to occur where their ranges overlap. In the region of geographical overlap, most populations of O. filiformis are strigillose in the inflorescences and have evening-opening flowers, while O. lindheimeri is villous in the inflorescences, and has large morning-opening flowers. Moreover, O. lindheimeri occurs only on black clay prairie soil, while O. filiformis occurs in light, sandy soil, as it does throughout its range, and in more disturbed areas. Despite these differences, Raven and Gregory found hybridization between these species scattered across an area from eastern Texas across Louisiana to Alabama. At some locations there is apparently no hybridization, while at others hybrids were uncommon to relatively common. Intermediate morning-blooming plants in Alabama appear to represent evidence of past hybridization since O. lindheimeri does not occur there. Many of the individuals they tested had somewhat reduced pollen fertility (40–70% fertile). They suspected that habitat disturbance was primarily responsible in many cases, but they also detected what may have been intergradation resulting from past hybridization outside of the current distribution of O. lindheimeri. Many of these individual cases deserve further investigation to better understand the dynamics of the interactions between these species and if any of the interactions have led to stabilization of novel populations that might be recognized taxonomically. Very few collections have been made from areas on the periphery of the range of Oenothera filiformis (southern Ontario, Connecticut, Maryland, Massachusetts, Pennsylvania), and populations in these areas probably represent recent human-based introductions. P. H. Raven and D. P. Gregory (1972[1973]) determined O. filiformis to be self-incompatible. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Oenothera jamesii has plastome I and a AA genome composition; it is known in the flora area from southern Kansas (Clark County), central Oklahoma, and Texas. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 10. | FNA vol. 10. |
Parent taxa | ||
Sibling taxa | ||
Synonyms | Gaura filiformis, G. biennis var. pitcheri, G. filiformis var. kearneyi, G. longiflora | Onagra jamesii, O. communis var. jamesii |
Name authority | (Small) W. L. Wagner & Hoch: Syst. Bot. Monogr. 83: 212. (2007) | Torrey & A. Gray: Fl. N. Amer. 1: 493. (1840) |
Web links |