Oenothera psammophila
Oenothera filiformis
St. Anthony dunes evening primrose
bee-blossom, longflower beeblossom
decumbent, usually branched, 10–30 cm, becoming woody and buried in sand.
usually well-branched distal to base, (50–)100–400 cm.
(6–)8–9(–14.2) × (0.7–)1.5–2(–3.1) cm;
petiole 3–9 cm;
blade narrowly oblanceolate to oblanceolate, margins usually subentire or repand or remotely dentate, rarely serrate, apex acute.
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.
1–3 per stem opening per day near sunset, with sweet scent;
buds erect;
floral tube 42–60 mm;
sepals 22–28 mm;
petals white, fading rose pink to rose, 23–40 mm;
filaments 17–19 mm, anthers 13–16 mm;
style 60–72(–88) 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.
somewhat curved and often somewhat twisted, lanceoloid-cylindrical, nearly cylindrical, (20–)30–47 × 7–8 mm, gradually tapering to apex, 6–8 mm, dehiscent nearly throughout their length, valve margins with a conspicuous, irregular, wavy ridge;
pedicel 1–5 mm.
ellipsoid or ovoid, sharply 4-angled, 4.5–7 × 1.5–2.5 mm;
sessile.
numerous, in 2 distinct rows per locule, narrowly obovoid, 2.5–3 × 1.2–1.4 mm, embryo 7/8 of seed volume, surface finely reticulate;
seed collar with a broad membrane sealing cavity, margin entire.
2–4, yellowish to reddish brown, 1.3–3 × 0.7–1.3 mm.
= 14.
= 14.
Oenothera psammophila
Oenothera filiformis
Oenothera psammophila is known only from the dune area north and west of St. Anthony, Fremont County. It is unique in Oenothera because of the exudate produced on the leaves to which sand particles adhere, forming a sand sheath, presumably for protection from the constantly blowing sand particles. It is self-incompatible (W. L. Wagner et al. 1985; Wagner 2005).
(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.)
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