Chylismia claviformis |
Chylismia parryi |
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brown-eyed primrose, browneyes, clavate fruit primrose |
redclay suncup |
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Habit | Herbs annual, glabrous, strigillose, glandular puberulent, or, sometimes, villous. | Herbs annual, sparsely to densely villous throughout or, sometimes, glabrate distally. | ||||||||||||||||||||||||||||||||||||
Stems | branched mostly from base, 3–70 cm. |
often intricately branched, 5–80 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 poorly defined basal rosette and also cauline; petiole 0.3–3.8 cm; blade usually unlobed, very rarely pinnately lobed with few, small lateral lobes, ovate to elliptic, margins sparsely denticulate to subentire, pale or dark brown oil cells lining veins abaxially. |
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Racemes | nodding, elongating after anthesis. |
nodding, with intricate, filiform branches, elongating in fruit. |
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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 without free tips; floral tube 0.5–2 mm, glabrous or villous inside; sepals 1.5–4 mm; petals bright yellow, often with red dots near base, fading pale yellow or yellowish orange, 2–7 mm; stamens unequal, filaments of antisepalous stamens 1.7–3.5 mm, those of antipetalous ones 1.2–2.5 mm, anthers 0.9–1.2 mm, glabrous; style 4–9 mm, stigma exserted beyond anthers at anthesis. |
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Capsules | ascending to spreading, clavate, 8–40 mm; pedicel 4–40 mm. |
erect or ascending, clavate, 4–10 mm; pedicel 4–20 mm. |
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Seeds | 0.6–1.5 mm. |
0.7–1.2 mm. |
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2n | = 14. |
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Chylismia claviformis |
Chylismia parryi |
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Phenology | Flowering May–Jun(–Sep). | |||||||||||||||||||||||||||||||||||||
Habitat | Red clay and sand slopes weathered from red (freshwater-deposited) sandstone cliffs, with Juniperus or Larrea tridentata. | |||||||||||||||||||||||||||||||||||||
Elevation | 800–1300 m. [2600–4300 ft.] | |||||||||||||||||||||||||||||||||||||
Distribution | w United States; nw Mexico
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AZ; UT
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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.) |
Chylismia parryi is known from northwestern Arizona (Coconino to Mohave counties) and southwestern Utah (Beaver to Washington counties), and is apparently disjunct to San Juan County, Utah. It is outcrossing and, perhaps, self-incompatible (P. H. Raven 1962, 1969). There are two morphological forms of this species. Raven (1962) noted that a later flowering form has narrower, smaller leaves, and less overall pubescence. It is not clear what these represent, but Raven (1962) made the combination Oenothera parryi forma tenuissima (M. E. Jones) P. H. Raven for it. He later (Raven 1969) noted that these plants did not seem to merit formal recognition, without any discussion. (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 | ||||||||||||||||||||||||||||||||||||||
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Synonyms | Oenothera claviformis, Camissonia claviformis, C. scapoidea var. claviformis, O. scapoidea var. claviformis | Oenothera parryi, Camissonia parryi, C. tenuissima, O. scapoidea var. parryi, O. tenuissima | ||||||||||||||||||||||||||||||||||||
Name authority | (Torrey & Frémont) A. Heller: Muhlenbergia 2: 105. (1906) — (as Chylisma clavaeformis) | (S. Watson) Small: Bull. Torrey Bot. Club 23: 193. (1896) — (as Chylisma) | ||||||||||||||||||||||||||||||||||||
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