Gayophytum diffusum |
Gayophytum diffusum subsp. parviflorum |
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diffuse groundsmoke, spreading groundsmoke |
Nuttall's groundsmoke, small flower groundsmoke, spreading groundsmoke |
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Habit | Herbs usually glabrous to strigillose, sometimes villous. | |||||
Stems | erect, branched or unbranched near base, much branched distally, usually with 1 or 2 nodes between branches, distal branching dichotomous or lateral branches shortened, 5–60 cm. |
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Leaves | reduced distally, 10–60 × 1–5 mm; petiole 0–10 mm; blade very narrowly lanceolate. |
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Inflorescences | with flowers arising usually as proximally as first 1–20 nodes from base. |
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Flowers | sepals 0.9–3(–5) mm, reflexed singly or in pairs; petals 1.2–5(–7) mm; pollen 90–100% fertile; stigma hemispheric to subglobose, exserted beyond anthers of longer stamens or surrounded by them at anthesis. |
sepals 0.9–2 mm; petals 1.2–3 mm; stigma subglobose, surrounded by anthers at anthesis. |
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Capsules | ascending to reflexed, subterete, 3–15 × 1–1.5 mm, with inconspicuous or conspicuous constrictions between seeds, valve margins somewhat undulate, all valves free from septum after dehiscence, septum straight or sinuous; pedicel 2–10(–15) mm, usually shorter than capsule. |
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Seeds | (3–)6–18, all or most developing, arranged ± parallel to septum and in alternating pattern between locules, crowded, overlapping, often appearing to form 2 irregular rows in each locule, or well spaced, forming a single row in capsule, brown, sometimes mottled with gray, 1–1.6 × 0.5–0.8 mm, glabrous or puberulent. |
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2n | = 28. |
= 28. |
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Gayophytum diffusum |
Gayophytum diffusum subsp. parviflorum |
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Phenology | Flowering Jun–Oct. | |||||
Habitat | Open pine forests, sagebrush slopes, dry margins of meadows. | |||||
Elevation | 800–3700 m. (2600–12100 ft.) | |||||
Distribution |
w North America; n Mexico
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AZ; CA; CO; ID; MT; NM; NV; OR; SD; UT; WA; WY; BC; Mexico (Baja California) |
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Discussion | Subspecies 2 (2 in the flora). Gayophytumdiffusum consists of a diverse assemblage of tetraploid populations, some of which are similar to every known diploid species except G. humile. The combination of characteristics of at least five diploid species in various ways suggests that the complex is derived from several independently formed allopolyploids that subsequently hybridized and segregated to produce the observed diversity. Populations of Gayophytum diffusum differ in breeding behavior. Populations with relatively large flowers and stigmas that extend beyond the anthers are obviously outcrossing, whereas most populations are small-flowered and modally self-pollinated. It is among the latter that the greatest morphological diversity is found. Often two or more morphologically different, apparently true-breeding strains can be found growing together. In such a variable complex, recognition of infraspecific taxa becomes arbitrary. In this treatment the striking morphological differences associated with breeding behavior have been used as a basis for subspecies recognition. At some localities the two subspecies intergrade. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Subspecies parviflorum is extremely variable and may sometimes closely resemble diploid species Gayophytum decipiens, G. heterozygum, G. oligospermum, and G. ramosissimum, the first of which are hypothesized to have been involved in its origin and variation (H. Lewis and J. Szweykowski 1964). (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 | Onagraceae > subfam. Onagroideae > tribe Onagreae > Gayophytum | Onagraceae > subfam. Onagroideae > tribe Onagreae > Gayophytum > Gayophytum diffusum | ||||
Sibling taxa | ||||||
Subordinate taxa | ||||||
Synonyms | G. diffusum var. strictipes, G. lasiospermum, G. lasiospermum var. hoffmannii, G. nuttallii var. abramsii, G. nuttallii var. intermedium, G. ramosissimum var. strictipes | |||||
Name authority | Torrey & A. Gray: Fl. N. Amer. 1: 513. (1840) | H. Lewis & Szweykowski: Brittonia 16: 386, figs. 5B, 17B. (1964) | ||||
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