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prairie beeblossom

bee-blossom, longflower beeblossom

Habit Herbs annual, villous proximally, sparsely villous along veins and on margins, usually glabrate, sometimes strigillose distally; from 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

ascending, usually well-branched from base and distally, rarely unbranched, 15–60 cm.

usually well-branched distal to base, (50–)100–400 cm.

Leaves

in a basal rosette and cauline, 1.5–8 × 0.2–0.6(–1.5) cm, blade very narrowly elliptic to oblanceolate or oblong-elliptic, margins entire or weakly sinuate-dentate.

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

3(or 4)-merous, zygomorphic, opening at sunset;

floral tube 4–5.5 mm;

sepals 4.5–6 mm;

petals white, fading pink, elliptic-obovate, 3.5–5 mm;

filaments 2–3.5 mm, anthers 1.5–3 mm, pollen 35–65% fertile;

style 9–10 mm, stigma surrounded by anthers.

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

narrowly obovoid, 3(or 4)-winged, furrowed between wings, 7–9 × 3–5 mm, narrowed at base;

sessile.

ellipsoid or ovoid, sharply 4-angled, 4.5–7 × 1.5–2.5 mm;

sessile.

Seeds

(1 or)2–5, yellowishto light brown, 1.5–3.5 × 1–1.5 mm.

2–4, yellowish to reddish brown, 1.3–3 × 0.7–1.3 mm.

2n

= 14.

= 14.

Oenothera triangulata

Oenothera filiformis

Phenology Flowering Apr–Jul. Flowering (Jun–)Jul–Oct(–Nov).
Habitat Open, sandy sites. Open woods, fields, along streams, sandy soil, disturbed sites, ditch banks, roadsides, railway embankments.
Elevation 200–600 m. (700–2000 ft.) 10–500 m. (0–1600 ft.)
Distribution
from FNA
OK; TX
[BONAP county map]
from FNA
AL; AR; CO; CT; IA; IL; IN; KS; KY; LA; MA; MD; MI; MO; MS; NE; OH; OK; PA; TN; TX; WI; ON
[WildflowerSearch map]
[BONAP county map]
Discussion

Oenothera triangulata is a PTH species and forms a ring of 14 chromosomes in meiosis. The species is self-compatible and autogamous (P. H. Raven and D. P. Gregory 1972[1973]). It may have been derived from hybridization between O. patriciae and O. suffulta. The species has a relatively narrow distribution across south-central Oklahoma and north-central Texas (Oklahoma in Cleveland, Comanche, Cotton, Grady, Oklahoma, Rogers, Stephens, and Tulsa counties; Texas in Archer, Baylor, Callahan, Clay, Coleman, Crosby, Eastland, Erath, Jones, Montague, Taylor, Throckmorton, Tom Greene, Wichita, Wilbarger, and Young counties).

(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 Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Gaura > subsect. Gaura Onagraceae > subfam. Onagroideae > tribe Onagreae > Oenothera > sect. Gaura > subsect. Gaura
Sibling taxa
O. acutissima, O. albicaulis, O. argillicola, O. arida, O. arizonica, O. biennis, O. boquillensis, O. brachycarpa, O. calcicola, O. californica, O. canescens, O. capillifolia, O. cavernae, O. cespitosa, O. cinerea, O. clelandii, O. coloradensis, O. cordata, O. coronopifolia, O. coryi, O. curtiflora, O. curtissii, O. deltoides, O. demareei, O. dodgeniana, O. drummondii, O. elata, O. engelmannii, O. falfurriae, O. filiformis, O. filipes, O. flava, O. fruticosa, O. gaura, O. gayleana, O. glaucifolia, O. glazioviana, O. grandiflora, O. grandis, O. harringtonii, O. hartwegii, O. havardii, O. heterophylla, O. hispida, O. howardii, O. humifusa, O. jamesii, O. kunthiana, O. laciniata, O. lavandulifolia, O. lindheimeri, O. linifolia, O. longissima, O. macrocarpa, O. mckelveyae, O. mexicana, O. nealleyi, O. neomexicana, O. nutans, O. nuttallii, O. oakesiana, O. organensis, O. pallida, O. parviflora, O. patriciae, O. perennis, O. pilosella, O. platanorum, O. podocarpa, O. primiveris, O. psammophila, O. pubescens, O. rhombipetala, O. riparia, O. rosea, O. serrulata, O. sessilis, O. simulans, O. sinuosa, O. spachiana, O. speciosa, O. stricta, O. suffrutescens, O. suffulta, O. tetraptera, O. texensis, O. toumeyi, O. triloba, O. tubicula, O. villosa, O. wolfii, O. xylocarpa
O. acutissima, O. albicaulis, O. argillicola, O. arida, O. arizonica, O. biennis, O. boquillensis, O. brachycarpa, O. calcicola, O. californica, O. canescens, O. capillifolia, O. cavernae, O. cespitosa, O. cinerea, O. clelandii, O. coloradensis, O. cordata, O. coronopifolia, O. coryi, O. curtiflora, O. curtissii, O. deltoides, O. demareei, O. dodgeniana, O. drummondii, O. elata, O. engelmannii, O. falfurriae, O. filipes, O. flava, O. fruticosa, O. gaura, O. gayleana, O. glaucifolia, O. glazioviana, O. grandiflora, O. grandis, O. harringtonii, O. hartwegii, O. havardii, O. heterophylla, O. hispida, O. howardii, O. humifusa, O. jamesii, O. kunthiana, O. laciniata, O. lavandulifolia, O. lindheimeri, O. linifolia, O. longissima, O. macrocarpa, O. mckelveyae, O. mexicana, O. nealleyi, O. neomexicana, O. nutans, O. nuttallii, O. oakesiana, O. organensis, O. pallida, O. parviflora, O. patriciae, O. perennis, O. pilosella, O. platanorum, O. podocarpa, O. primiveris, O. psammophila, O. pubescens, O. rhombipetala, O. riparia, O. rosea, O. serrulata, O. sessilis, O. simulans, O. sinuosa, O. spachiana, O. speciosa, O. stricta, O. suffrutescens, O. suffulta, O. tetraptera, O. texensis, O. toumeyi, O. triangulata, O. triloba, O. tubicula, O. villosa, O. wolfii, O. xylocarpa
Synonyms Gaura triangulata, G. hexandra var. triangulata, G. tripetala var. triangulata Gaura filiformis, G. biennis var. pitcheri, G. filiformis var. kearneyi, G. longiflora
Name authority (Buckley) W. L. Wagner & Hoch: Syst. Bot. Monogr. 83: 214. (2007) (Small) W. L. Wagner & Hoch: Syst. Bot. Monogr. 83: 212. (2007)
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