Chylismia claviformis |
Chylismia walkeri |
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brown-eyed primrose, browneyes, clavate fruit primrose |
Walker's evening-primrose, Walker's sun-cup |
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Habit | Herbs annual, glabrous, strigillose, glandular puberulent, or, sometimes, villous. | Herbs annual or short-lived perennial, villous, usually densely so proximally, less dense to glabrate distally, sometimes hairs somewhat appressed and shorter on leaves, also sometimes glandular puberulent on distal parts. | ||||||||||||||||||||||||||||||||||||||||
Stems | branched mostly from base, 3–70 cm. |
slender, unbranched or branched from base, 10–60 cm. |
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Leaves | primarily in basal rosette, cauline reduced or absent, 1.5–20 × 0.3–3.5 cm; petiole 0.7–12 cm; blade usually pinnately lobed, sometimes lateral lobes poorly developed or absent, terminal lobe usually narrowly ovate to lanceolate, sometimes cordate or subcordate, 0.8–9 × 0.2–4.5 cm, margins dentate, sinuate-dentate, or serrate, brown oil cells conspicuously lining veins abaxially. |
in basal rosette and/or cauline, often purple-dotted, 2–22 × 0.4–3.5 cm; petiole 0.4–8 cm; blade pinnately lobed, sometimes lateral lobes greatly reduced or absent and blade reduced to terminal lobe only, terminal lobe oblong or cordate to ovate, 1–5 × 0.5–3.2 cm, margins serrate, brown oil cells prominently lining veins abaxially. |
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Racemes | nodding, elongating after anthesis. |
erect, elongating after anthesis. |
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Flowers | opening at sunset or sunrise; buds with or without subapical or apical free tips; floral tube 2–6.5 mm, villous inside proximally; sepals 2–8 mm; petals pale to bright yellow or white, sometimes red- or purple-dotted near base, fading purple, sometimes red or orange, or not changing color, 1.5–8 mm; stamens subequal, filaments 1.5–5.5 mm, anthers 1.5–6 mm, ciliate; style 5–16 mm, stigma exserted beyond anthers at anthesis. |
opening at sunrise; buds individually reflexed, with apical free tips less than 1 mm; floral tube 0.5–1.5 mm, glabrous or sparsely villous inside; sepals 1.5–5 mm; petals bright yellow, fading pale orange or lavender, 1–6 mm; stamens unequal, filaments of antisepalous stamens 1–3 mm, those of antipetalous ones 0.3–2 mm, anthers 0.5–2 mm, glabrous or sparsely ciliate; style 1.5–6 mm, stigma surrounded by anthers at anthesis. |
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Capsules | ascending to spreading, clavate, 8–40 mm; pedicel 4–40 mm. |
spreading or ascending, oblong-cylindrical, 11–45 mm; pedicel 5–30 mm. |
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Seeds | 0.6–1.5 mm. |
0.6–1.2 mm. |
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Chylismia claviformis |
Chylismia walkeri |
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Distribution | w United States; nw Mexico
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sw United States
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Discussion | Subspecies 11 (10 in the flora). P. H. Raven (1962) subdivided this species into 12 subspecies and, subsequently (1969), he combined two of them. The latter approach is used here. Only subsp. wigginsii P. H. Raven does not occur in the United States; its narrow range is restricted to northern Baja California. Raven (1962, 1969) determined this species to be self-incompatible. Chylismia claviformis is the most complex and, along with C. scapoidea, the most widely distributed species of the genus. The central part of its geographical range is occupied by five closely related white-petaled subspecies (aurantiaca, claviformis, funerea, integrior, and peeblesii) that are very similar morphologically. South of this area four additional subspecies occur, all yellow-petaled (peirsonii, rubescens, wigginsii, and yumae). These four subspecies have sepals and petal color similar to those of C. brevipes, and P. H. Raven (1962, 1969) thought it likely that they were derived following hybridization between that species and one of the white-petaled populations of C. claviformis. North of the range of the white-petaled subspecies are found two additional yellow-petaled subspecies (cruciformis and lancifolia). Most populations of subsp. cruciformis consist of plants in which the flowers open in the early morning; in all other subspecies the flowers open in the late afternoon (Raven 1962, 1969). The following key will separate them, but there are many intergrades among the subspecies so that not all specimens will be easily identified. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Subspecies 2 (2 in the flora). P. H. Raven (1962, 1969) determined this species to be self-incompatible and primarily autogamous. (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 | ||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||||||||||||||||||||||
Synonyms | Oenothera claviformis, Camissonia claviformis, C. scapoidea var. claviformis, O. scapoidea var. claviformis | Camissonia walkeri, Oenothera walkeri | ||||||||||||||||||||||||||||||||||||||||
Name authority | (Torrey & Frémont) A. Heller: Muhlenbergia 2: 105. (1906) — (as Chylisma clavaeformis) | A. Nelson: Bot. Gaz. 56: 66. (1913) — (as Chylisma) | ||||||||||||||||||||||||||||||||||||||||
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