Oenothera nealleyi |
Oenothera filiformis |
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bee-blossom, longflower beeblossom |
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Habit | Herbs annual, sparsely villous proximally, leaves glabrate to sparsely villous along veins and on margins, usually glandular puberulent in distal parts; from stout taproot. | Herbs usually robust winter-annual, sometimes biennial, moderately to densely strigillose, sometimes also glandular puberulent, villous and/or short-hirtellous; from fleshy taproot. |
Stems | usually well-branched, 20–70(–100) cm. |
usually well-branched distal to base, (50–)100–400 cm. |
Leaves | in a basal rosette and cauline, basal 3.5–9 × 0.5–1.5 cm, blade lyrate; cauline 1.5–7 × 0.1–0.6 cm, blade narrowly lanceolate to linear, margins sinuate-dentate, undulate. |
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. |
Flowers | 4-merous, zygomorphic, opening at sunset; floral tube 10–20 mm; sepals 11–21 mm; petals white, fading pink to red, elliptic to elliptic-obovate, 10–15 mm; filaments 8–13 mm, anthers 2–6 mm, pollen 90–100% fertile; style 22–36 mm, stigma exserted beyond anthers at anthesis. |
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. |
Capsules | ellipsoid or ovoid, narrowly 4-winged, furrowed between angles, 4.5–8 × 2–5 mm, stipe 0.2–2.2 mm; sessile. |
ellipsoid or ovoid, sharply 4-angled, 4.5–7 × 1.5–2.5 mm; sessile. |
Seeds | 3 or 4 (or 5), yellowish to light brown, 2–3(–4) × 1 mm. |
2–4, yellowish to reddish brown, 1.3–3 × 0.7–1.3 mm. |
2n | = 14. |
= 14. |
Oenothera nealleyi |
Oenothera filiformis |
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Phenology | Flowering Apr–Oct. | Flowering (Jun–)Jul–Oct(–Nov). |
Habitat | Washes, sandy places, grasslands, extending to pinyon-juniper woodlands. | Open woods, fields, along streams, sandy soil, disturbed sites, ditch banks, roadsides, railway embankments. |
Elevation | 1200–2200 m. (3900–7200 ft.) | 10–500 m. (0–1600 ft.) |
Distribution |
NM; TX; Mexico (Coahuila) |
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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Discussion | Oenothera nealleyi is restricted to an area from trans-Pecos Texas and northern Coahuila, Mexico, north to Bernalillo and Torrance counties, New Mexico. P. H. Raven and D. P. Gregory (1972[1973]) considered O. nealleyi to represent an unevenly intergrading entity with O. suffulta based on merging of distinguishing characteristics. The known intermediates occur in Terrell County, Texas, and were previously described as Gaura suffulta var. terrellensis Munz, but until new data on its status are available, we include this name with O. nealleyi. The molecular data (K. N. Krakos, unpubl.) suggest that O. nealleyi is not as closely related to O. suffulta as suggested by Raven and Gregory, given the placement in the phylogeny and the difference in scent profiles for these two taxa. Oenothera suffulta is a member of a strongly supported clade that also includes O. patriciae and O. triangulata, while O. nealleyi is a member of a polytomy that consists of other species of subsect. Gaura, with the O. suffulta—O. triangulata—O. patriciae clade sister to it (W. L. Wagner et al. 2013). Oenothera nealleyi has a strong sweet scent, whereas O. suffulta does not have a discernible scent (Wagner et al.). Raven and Gregory determined O. nealleyi to be self-incompatible. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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.) |
Source | FNA vol. 10. | FNA vol. 10. |
Parent taxa | ||
Sibling taxa | ||
Synonyms | Gaura nealleyi, G. suffulta subsp. nealleyi, G. suffulta var. terrellensis, O. suffulta subsp. nealleyi | Gaura filiformis, G. biennis var. pitcheri, G. filiformis var. kearneyi, G. longiflora |
Name authority | (J. M. Coulter) Krakos & W. L. Wagner: PhytoKeys 28: 64. (2013) | (Small) W. L. Wagner & Hoch: Syst. Bot. Monogr. 83: 212. (2007) |
Web links |