Portulacaceae |
Phemeranthus |
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purslane family |
fameflower, flameflower |
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Habit | Subshrubs [shrubs] or herbs, annual, biennial, or perennial, often succulent or fleshy. | Herbs, perennial, caulescent (subscapose in P. humilis), glabrous. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Roots | sometimes tuberous, fleshy to woody. |
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Stems | ascending to erect, simple or branching, sometimes suffrutescent. |
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Leaves | opposite, subopposite, or alternate and sometimes secund, sometimes rosulate or subrosulate, exstipulate (except Portulaca and Talinopsis, with nodal or axillary hairs regarded as stipular); blade margins mostly entire, occasionally dentate to crisped. |
alternate or subopposite, sometimes subrosulate, petiolate or sessile, articulate at base, not clasping but sometimes with auriculate, membranous to chartaceous basal enations, attachment point round; blade terete, semiterete, or narrowly planate, 1–3 (10–20 in P. aurantiacus) mm wide, succulent (semisucculent in P. aurantiacus, P. sediformis, and P. spinescens). |
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Inflorescences | axillary or terminal, cymose, racemose, paniculate, or umbellate, sometimes glomerate, spikelike, or with flowers solitary, open to congested. |
lateral and/or terminal (lateral sometimes appearing terminal due to congestion of leaves on very short stems), cymose or cymulose, not appearing secund, few- to many-flowered, or flowers solitary and axillary; peduncle very short to elongate, sometimes scapelike. |
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Flowers | mostly radially symmetric, sometimes slightly irregular (in Montia); sepals 2–9; petals (1–)2–19 or sometimes absent, distinct or connate basally; stamens 1–many, opposite and sometimes basally adnate to petals; gynoecium 2–9-carpelled; ovary 1, superior (half-inferior to inferior in Portulaca), 1-locular throughout or initially plurilocular and becoming 1-locular distally (in Portulaca), placentation basal or free-central, ovules 1-many; style present, sometimes branched, or absent; stigmas 1–9. |
pedicellate (sometimes subsessile or sessile in P. parviflorus), each opening for 2–4 hours from afternoon to early evening of a single day, sometimes facultatively cleistogamous; sepals promptly deciduous after anthesis or persistent through capsule development, distinct; petals fugacious, 5 or rarely more, distinct or sometimes basally connate; stamens 4–many, distinct or with filaments basally shortly coherent in several clusters, anther 2-locular, oblong (subglobose in P. rugospermus); gynoecium 3[–5]-carpelled, placentention free-central; style 1 [absent]; stigmas 1 or 3[–5]. |
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Fruits | capsular. |
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Capsules | longitudinally dehiscent from apex, 3-valved; valves deciduous, erect, exocarp and endocarp not evidently differentiated and not separating. |
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Seeds | smooth or sculptured, with or without strophioles or elaiosomes. |
many, black or brown, ± compressed, with or without ± parallel, arcuate ridges, estrophiolate, circular-reniform, small; seed coat lustrous, smooth (corrugate-rugulose in P. rugospermus), covered with pale white or gray, thin, dull, fleshy to chartaceous pellicle. |
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x | = 4–9, 11, 13, 15, 23. |
= 12. |
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Portulacaceae |
Phemeranthus |
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Distribution | Primarily Southern Hemisphere; poorly represented in Eurasia |
North America; Central America; South America |
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Discussion | Genera 20–30, species ca. 500 (9 genera, 91 species in the flora). The eastern New World species of Portulacaceae seem to have a closer relationship with the African species, and the western New World species a closer one with the Australian species, than the two New World groups have with each other to each other. The outer perianth segments, referred to herein as sepals, are held by some (e.g., T. Eckardt 1976) to be modified bracteoles, the petals then representing the true sepals. However, the traditional interpretation, adopted here and in most North American floras, still finds current support (R. C. Carolin 1987). A comparable situation prevails with respect to the cauline leaves in Claytonia and other genera, which are widely interpreted to be foliaceous bracts (R. C. Carolin 1987); here again, as is appropriate in a descriptive context, the traditional terminology is employed. In Talinopsis and Portulaca, the stipular nature of the nodal or axillary hairs also has been a matter of discussion. The question was revisited by R. Geesink (1969), who denied their stipular origin. The relationships of the family are not a matter of dispute (A. Cronquist 1981; R. C. Carolin 1987); the same cannot be said for the relationships and delimitations of the genera, which have always been labile. They are, at present, the subject of active research, which has led to the current acceptance of Phemeranthus and Cistanthe. Changes in the generic classification are discussed in the treatments of the genera concerned. Because of the uncertain relationships, the genera and species are listed alphabetically. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Species 25–30 (16 in the flora). C. S. Rafinesque (1814b) transferred Pursh’s Talinum teretifolium, which had been described earlier that year and was the only North American species then attributed to that primarily Old World genus, to the segregate genus Phemeranthus. Since then, though, most other authors have continued to recognize that species within Talinum, along with other similar and exclusively New World taxa described subsequently, as sect. Phemeranthus. However, a fairly strongly correlated set of differences in the leaf, pollen, fruit, and seed structures of these species compared with those of sect. Talinum, only two species of which are found in North America, supports their recognition at the generic level (R. Carolin 1987, 1993; M. A. Hershkovitz 1993). Complementary to the morphological evidence, recent molecular studies (M. A. Hershkovitz and E. A. Zimmer 1997, 2000; W. L. Applequist and R. S. Wallace 2001) indicate that Phemeranthus is phylogenetically distinct from Talinum. Positive identification of Phemeranthus specimens often requires examination of both flower and fruit, including seeds (with hand lens). Fortunately, the flowers develop successively and the capsules mature rapidly after anthesis, so both flowers and fruits will be present on a given plant during most of the reproductive season. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Source | FNA vol. 4, p. 457. | FNA vol. 4, p. 488. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Synonyms | Talinum section P. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | Adanson | Rafinesque: Specchio Sci. 1: 86. (1814) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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