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bee-blossom, longflower beeblossom

Howard's 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 acaulescent or sometimes caulescent, moderately to densely strigillose and glandular puberulent, sometimes also sparsely to moderately hirsute; from a taproot, sometimes lateral roots producing adventitious shoots.
Stems

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

(when present) ascending, longer ones becoming decumbent, leafy, sometimes densely so, 0–10(–30) 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, sometimes also cauline, (6–)8.5–17(–23) × (0.5–)1–2(–3) cm;

petiole 2–7.5 cm;

blade usually oblanceolate, elliptic to narrowly oblong, rarely lanceolate, margins often undulate, entire or remotely and irregularly pinnately lobed mostly in proximal 1/2, rarely more regularly pinnately lobed and lobing extending to distal 1/2, sinuses usually extending less than 1/2 to midrib, lobes triangular to oblong or linear, (1–)4–9(–13) mm, apex acute to obtuse.

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.

usually 1 or 2, rarely more, opening per day near sunset, strongly and sweetly scented;

buds with unequal free tips 1–3(–4) mm;

floral tube (43–)60–110(–125) mm;

sepals (30–)35–60(–80) mm;

petals brilliant yellow, fading deep red, drying deep reddish purple to reddish brown, usually broadly obovate, rarely subrhombic, (30–)40–60(–73) mm, sometimes with a terminal tooth;

filaments (19–)25–38 mm, anthers 10–17 mm;

style(90–)110–145(–165) mm, stigma exserted beyond anthers at anthesis.

Capsules

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

sessile.

leathery, ovoid, narrowly ovoid, or narrowly lanceoloid to broadly ellipsoid, winged, wings (2–)4–7(–11) mm wide, body (20–)25–50(–80) × 4–6 mm, dehiscent 1/4–1/3 their length;

pedicel 2–6 mm.

Seeds

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

numerous, usually in 1 row per locule, rarely in 2 rows toward base, obovoid to subcuboid, 3–8 × 2.5–3.5 mm.

2n

= 14.

= 28, 42, 56.

Oenothera filiformis

Oenothera howardii

Phenology Flowering (Jun–)Jul–Oct(–Nov). Flowering May–Jul.
Habitat Open woods, fields, along streams, sandy soil, disturbed sites, ditch banks, roadsides, railway embankments. Open or rocky areas, in shale, fine-textured sandstones, clays, gypsum, or limestone from High Plains grasslands, open sites in pinyon-juniper woodlands, ponderosa pine-Douglas fir forests.
Elevation 10–500 m. (0–1600 ft.) (1000–)1500–2300(–3000) m. ((3300–)4900–7500(–9800) ft.)
Distribution
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]
from FNA
CO; KS; NV; UT; WY
[WildflowerSearch map]
[BONAP county map]
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.)

Oenotherahowardii is known from three disjunct areas: three collections on the High Plains (Baca and Otero counties, Colorado, and Hamilton County, Kansas); open yucca-juniper grassland, rocky slopes or disturbed areas on shale substrates along the Colorado counties of Boulder, Denver, Jefferson, and Larimer, and just over the state line in Wyoming; and, common to scattered, mostly on rocky slopes but also in shaded canyon sites on fine-textured red sandstones, clays, gypsum, chalky white degraded limestone or limestone in pinyon-juniper woodland to ponderosa pine-Douglas fir forest in southern Utah and eastern Nevada.

A. Nelson intended to publish Lavauxia howardii as a new combination and base it on Oenothera howardii M. E. Jones (1893), which was not validly published at the time, but inadvertently published L. howardii as a new species. Oenothera howardii (A. Nelson) W. L. Wagner is an isonym.

(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. Megapterium
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. 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
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. 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 filiformis, G. biennis var. pitcheri, G. filiformis var. kearneyi, G. longiflora Lavauxiahowardii a.
Name authority (Small) W. L. Wagner & Hoch: Syst. Bot. Monogr. 83: 212. (2007) (A. Nelson) M. E. Jones ex Prain in B. D. Jackson et al.: Index Kew., suppl. 3: 121. (1908) — (as howardi)
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