Portulacaceae |
Talinopsis |
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purslane family |
talinopsis |
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Habit | Subshrubs [shrubs] or herbs, annual, biennial, or perennial, often succulent or fleshy. | Subshrubs. | ||||||||||||||||||||||||||||||||||||||||
Roots | tuberous. |
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Stems | branching, suffrutescent, glabrous except at nodes; young branches slender, nodes dilated, tufted-pubescent. |
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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. |
opposite, sometimes in axillary fascicles, sessile; blade subterete, fleshy, margins entire. |
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Inflorescences | axillary or terminal, cymose, racemose, paniculate, or umbellate, sometimes glomerate, spikelike, or with flowers solitary, open to congested. |
lateral, cymose, few-flowered, axes angled; peduncle short. |
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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. |
sessile; sepals persistent, distinct; petals fugacious, 5, distinct; stamens 20–25, distinct, anther 2-locular, oblong; gynoecium 3-carpellate, ovary superior, placentation free-central, style 1, stigmas 3, dilated. |
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Fruits | capsular. |
capsular, longitudinally dehiscent from apex; valves persistent; exocarp and endocarp evidently differentiated and separating; exocarp 3-valved, valves recurving; endocarp 6-valved, valves erect. |
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Seeds | smooth or sculptured, with or without strophioles or elaiosomes. |
many, uncinate to arcuate, small, estrophiolate; seed coat granulate, pellicle absent. |
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x | = 4–9, 11, 13, 15, 23. |
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Portulacaceae |
Talinopsis |
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Distribution | Primarily Southern Hemisphere; poorly represented in Eurasia |
sw United States; n Mexico |
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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 1. A cladistic analysis of chloroplast ndhF sequence data (W. L. Applequist and R. S. Wallace 2001) indicated that Talinopsis is closely related to representatives of Anacampseros Linnaeus and Grahamia Gillies ex Hooker & Arnott (as originally suggested by A. Gray), in a clade not far removed from Talinum but fairly distant from the one that includes Phemeranthus mengesii and presumably the other species of that genus (except perhaps P. aurantiacus, which see). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 4, p. 457. | FNA vol. 4, p. 501. | ||||||||||||||||||||||||||||||||||||||||
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Name authority | Adanson | A. Gray: Smithsonian Contr. Knowl. 3(5): 14. (1852) | ||||||||||||||||||||||||||||||||||||||||
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