Camissonia |
Camissonia integrifolia |
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evening primrose, sun cup, suncups |
Kern River evening-primrose |
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Habit | Herbs, annual, caulescent; with a taproot. | Herbs sparsely strigillose or glabrate, more densely so distally. | ||||||||||||||||||||||||||||||||||||||||
Stems | erect, decumbent, or ascending, usually branched from base and distally, epidermis white or reddish brown, often exfoliating. |
usually erect, sometimes decumbent, slender, wiry, usually many-branched, to 30 cm. |
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Leaves | cauline, proximalmost often clustered near base, alternate; stipules absent; subsessile; blade margins entire, serrulate, or serrate. |
proximalmost not clustered near base; blade linear, 1–3 × 0.1–0.3 cm, base cuneate or attenuate, margins usually entire, rarely with 1 or 2 small teeth, apex acute. |
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Inflorescences | usually leafy spikes, sometimes racemes, nodding at anthesis, erect in fruit. |
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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 separately or in pairs; petals 4, yellow, fading red, often with red dots basally; stamens 8, in 2 unequal series, anthers versatile, pollen shed singly; ovary 4-locular, without apical projection, stigma subentire, subcapitate to subglobose, surface unknown, probably wet and non-papillate. |
opening near sunrise; floral tube 1.5–2.5 mm, moderately to sparsely pubescent inside on proximal 1/2; sepals 1.6–4 mm, reflexed in pairs; petals 2–4.2 mm, each ± with 2 red dots basally; episepalous filaments 0.9–2.1 mm, epipetalous filaments 0.5–1.4 mm, anthers 0.3–0.6 mm, pollen with usually less than 10% of grains 4-pored; style 2.3–4.8 mm, stigma surrounded by anthers at anthesis. |
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Fruit | a capsule, straight to flexuous, cylindrical, subterete, regularly, sometimes tardily, loculicidally dehiscent; usually sessile, sometimes pedicellate. |
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Capsules | 45–60 × 0.8–1.3 mm; subsessile. |
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Seeds | numerous, in 1 row per locule, narrowly obovoid to narrowly oblanceoloid, triangular in cross-section, appearing smooth, glossy. |
1–2 × 0.4–0.5 mm. |
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x |
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2n | = 28. |
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Camissonia |
Camissonia integrifolia |
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Phenology | Flowering Apr–May. | |||||||||||||||||||||||||||||||||||||||||
Habitat | Sagebrush slopes. | |||||||||||||||||||||||||||||||||||||||||
Elevation | 700–1000 m. (2300–3300 ft.) | |||||||||||||||||||||||||||||||||||||||||
Distribution |
w North America; nw Mexico; w South America |
CA; Mexico (Baja California) |
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Discussion | Species 12 (11 in the flora). Species of Camissonia occur in desert scrub, grasslands, or pinyon-juniper woodlands, on brushy or open slopes and flats, washes, and, sometimes, on serpentine barrens, at elevations 0 to 2300 meters. Camissonia campestris and C. kernensis are self-incompatible diploids; C. pusilla and C. sierrae are self-compatible diploids; C. contorta is an autogamous hexaploid; the other species are autogamous tetraploids. Identification of the polyploid species of Camissonia is aided by their pollen having a high proportion of grains with more pores, usually 4 or 5, than typical 3-pored pollen in Onagraceae. This can be observed under low magnification (for example, 10\×) since 3-pored pollen is triangular, while 4-pored is quadrangular, and 5-pored is pentangular. P. H. Raven (1969) delineated a group of four closely related species (Camissonia kernensis, C. parvula, C. pubens, and C. pusilla), marked by having sepals reflexed separately (rather than in pairs), which occur mainly in the Great Basin. Of the remaining species of Camissonia in the flora area, several (C. benitensis, C. campestris, C. integrifolia, C. lacustris, and C. sierrae) have more or less restricted ranges within California, or (C. strigulosa) extend also to Baja California, Mexico, or (C. contorta) to Washington, Idaho, and disjunctly to Vancouver Island, British Columbia. Camissonia dentata (Cavanilles) Reiche is the twelfth species in the genus, disjunct in western South America from southern Peru southward into Chile and Argentina. W. L. Wagner et al. (2007) departed significantly from the most recent monograph by P. H. Raven (1969) in the delimitation of Camissonia based on the molecular analysis (R. A. Levin et al. 2004); they recognized eight genera in addition to the much reduced Camissonia: Camissoniopsis, Chylismia, Chylismiella, Eremothera, Eulobus, Neoholmgrenia, Taraxia, and Tetrapteron. Raven noted that Camissonia was the most heterogeneous genus in Onagreae, consisting of sharply distinct sections. He further noted that the capitate or subglobose stigma found in Camissonia, by which he distinguished the genus from the broadly circumscribed Oenothera of P. A. Munz (1965), was also found in Gayophytum, Gongylocarpus Schlechtendal & Chamisso, and Xylonagra Donnell Smith & Rose, thus the primary defining character state for the genus at that time is a plesiomorphy (P. C. Hoch et al. 1993). The redefined Camissonia is morphologically delimited by having subterete capsules that are more or less swollen by seeds, linear to narrowly elliptic leaves, and glossy seeds that are triangular in cross-section and mostly smaller than 1 mm in length; and flowering only at the distal, not basal, nodes; and is without ultraviolet reflectance pattern on petals (Raven). Reproductive features include: self-incompatible (C. campestris, C. kernensis) or self-compatible; flowers diurnal; outcrossing and pollinated by bees (E. G. Linsley et al. 1963, 1963b, 1964, 1973), or autogamous, rarely cleistogamous (Raven). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Camissonia integrifolia is known in the flora area from central to southern California, west of the Sierra Nevada. P. H. Raven (1969) determined that Camissonia integrifolia is a self-compatible tetraploid and autogamous. The species forms sterile natural hybrids with C. strigulosa, to which it is presumably most closely related. (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. | ||||||||||||||||||||||||||||||||||||||||
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Synonyms | C. section sphaerostigma, Oenothera section sphaerostigma, Oenothera unraked sphaerostigma, Oenothera subg. sphaerostigma, Sphaerostigma | |||||||||||||||||||||||||||||||||||||||||
Name authority | Link: Jahrb. Gewächsk. 1(1): 186. (1818) | P. H. Raven: Contr. U.S. Natl. Herb. 37: 344, fig. 62. (1969) | ||||||||||||||||||||||||||||||||||||||||
Web links |