Eremothera |
Eremothera nevadensis |
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evening primrose, mooncup |
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Habit | Herbs, annual, caulescent; with a taproot. | Herbs glabrate to strigillose in distal and younger parts and capsules. | ||||||||||||||||||||||||
Stems | usually erect, sometimes ascending, usually well-branched from base, sometimes also distally, with white or reddish green exfoliating epidermis. |
branched from base, primary stem short, lateral stems decumbent, usually with leaves mostly in a tuft toward apex, 1–5(–18) cm, flowering proximally and distally. |
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Leaves | cauline, proximal ones often clustered near base, alternate; stipules absent; petiolate, often subsessile distally; blade margins denticulate, crenate-dentate, serrulate, sinuate-toothed, or entire. |
mostly cauline, clustered toward ends of branches, 1–4.5 × 0.2–0.8 cm; petiole 1–3 cm; blade oblanceolate or narrowly oblanceolate, margins entire. |
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Inflorescences | spikes, erect or nodding at anthesis, or flowers also in proximal leaf axils in some taxa. |
erect. |
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Flowers | bisexual, actinomorphic, buds erect; floral tube deciduous (with sepals, petals, and stamens) after anthesis, with basal nectary; sepals 4, reflexed singly or in pairs; petals 4, usually white, rarely red or tinged red, without spots, fading pink or red; stamens 8 in 2 unequal series, episepalous ones rarely abortive (E. minor), anthers versatile, pollen shed singly; ovary 4-locular, without apical projection, style villous near base, strigillose, or glabrous, stigma entire, subglobose, surface unknown, probably wet and non-papillate. |
opening at sunset; floral tube 2.2–3.5 mm, glabrous inside; sepals 3.2–4 mm; petals white, fading pinkish, 3–5 mm; episepalous filaments 4.5–4.8 mm, epipetalous filaments 3–4 mm, anthers 0.4–1.5 mm; style 6–7 mm, glabrous, stigma 0.5–0.8 mm diam., exserted beyond anthers at anthesis. |
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Fruit | a capsule, straight or much contorted, narrowly cylindrical throughout or thickened proximally, terete or 4-angled, regularly but tardily loculicidal; sessile. |
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Capsules | cylindrical and thickened proximally, spreading and highly contorted, 4-angled, 8–14 × 1–2 mm, regularly but tardily dehiscent. |
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Seeds | numerous, in 1 row per locule, usually monomorphic and narrowly obovoid to oblanceoloid, sometimes dimorphic, with seeds near base of capsule sharply angular and truncate-ellipsoid, finely reticulate, or seeds near base of capsule coarsely papillose. |
monomorphic, gray, 1.2–1.5 × 0.3–0.4 mm, finely reticulate. |
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2n | = 14. |
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Eremothera |
Eremothera nevadensis |
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Phenology | Flowering Apr–May(–early Jun). | |||||||||||||||||||||||||
Habitat | Local and colonial on clay, sandy, or gravelly soils, often vernally wet sites, somewhat tolerant of alkali soils. | |||||||||||||||||||||||||
Elevation | 1200–1700 m. (3900–5600 ft.) | |||||||||||||||||||||||||
Distribution | w United States; sc United States; nw Mexico |
NV |
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Discussion | Species 7 (7 in the flora). Species of Eremothera are found mainly in the interior deserts and bordering areas of the western United States. R. A. Levin et al. (2004) found strong molecular support for paraphyly in the broadly delimited Camissonia of P. H. Raven (1969). There was some support for a clade of Camissonia and Eremothera and another clade of Camissoniopsis, Neoholmgrenia, and Tetrapteron (Levin et al.), but without morphological features linking the members of these two clades. The monophyletic subclades of these two clades were recognized as genera by W. L. Wagner et al. (2007) whereas they were all treated by Raven as clearly distinguishable sections. Raven recognized four distinct groups within Eremothera (as Camissonia sect. Eremothera): E. refracta and its autogamous derivative, E. chamaenerioides; the very diverse E. boothii (with six subspecies) and two rare autogamous derivatives, E. gouldii and E. pygmaea; the local clay endemic E. nevadensis; and the widespread autogamous and often cleistogamous E. minor. Levin et al. included one species from each of these four groups in their molecular analyses and found strong support for Eremothera as circumscribed by Raven and maintained by Wagner et al. Eremothera is well defined by white petals that open in the evening and an entire, subglobose stigma; some species are visited by moths at anthesis and by bees the following morning (Raven). Reproductive features include: self-incompatible (E. boothii, E. refracta, and, possibly, E. nevadensis) or self-compatible; flowers vespertine; outcrossing and pollinated in the evening by small moths and the following morning by bees, in E. boothii subsp. decorticans by large oligolectic andrenid bees (E. G. Linsley et al. 1963, 1964, 1973), or autogamous, rarely cleistogamous (Raven). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Eremothera nevadensis is known only from west-central Nevada in western Churchill, Douglas, northern Lyon, Ormsby, Pershing, Storey, and southern Washoe counties. P. H. Raven (1969) presumed Eremothera nevadensis to be self-compatible. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 10. | FNA vol. 10. | ||||||||||||||||||||||||
Parent taxa | ||||||||||||||||||||||||||
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Synonyms | Camissonia section eremothera, Oenothera section eremothera | Oenothera nevadensis, Camissonia nevadensis, O. gauriflora var. caput-medusae, O. gauriflora var. vermiculatam., Sphaerostigma nevadense, S. tortuosum | ||||||||||||||||||||||||
Name authority | (P. H. Raven) W. L. Wagner & Hoch: Syst. Bot. Monogr. 83: 125. (2007) | (Kellogg) W. L. Wagner & Hoch: Syst. Bot. Monogr. 83: 210. (2007) | ||||||||||||||||||||||||
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