Atriplex glabriuscula |
Chenopodiaceae |
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bract orache, glabrous orach, scotland orache |
goosefoot family |
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Habit | Herbs, monoecious, prostrate or sprawling, or sometimes erect, branched, (1–)2–10 dm; branches opposite or subopposite. | Herbs, shrubs (rarely small trees), annual or perennial, monoecious, dioecious, or polygamous, evergreen or deciduous. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Roots | fibrous, taprooted, sometimes fusiform or bulbous, fleshy and thickened in Beta. |
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Stems | green and striped, often blue-green when fresh, weakly ridged, sparsely scurfy to glabrous. |
sometimes succulent and apparently jointed, or with slippery and aromatic bark, sometimes spiny, alternate or opposite; pubescence silvery, sometimes stellate or glandular, often scurfy from inflated salt glands that senesce into white flakes. |
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Leaves | petiole 0.2–2.5(–3.5) cm; blade all entire or some or all triangular or lance-hastate with lobes spreading to antrorse, 5–100 × 3–80 mm, base abruptly to narrowly cuneate, entire or irregularly toothed. |
simple, usually alternate, occasionally opposite, lacking stipules, petiolate or sessile, sometimes reduced to small scales, or fleshy; blade linear to broadly triangulate in outline, margins entire to serrate, serrate-dentate, or lobed. |
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Inflorescences | flowers solitary or clustered in axillary or terminal glomerules or in short, cylindric spikes; bracts absent or 1–5, deciduous or persistent, of various shapes. |
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Flowers | in loose glomerules, arranged in foliose, interrupted spikes or axillary, terminating stems and branches. |
bisexual or unisexual, uniseriate, radially or rarely bilaterally symmetric; bracteoles absent or 1–5, connate basally, green; perianth segments 5, sometimes 1 or absent, green, inconspicuous, fleshy in Salicornia and Sarcocornia, strongly imbricate in Nitrophila; petals absent; stamens absent or 1–5, usually as many as and opposite perianth lobes; pistils absent or (1–)2(–3); styles 1–3, sometimes with stylopodium; ovary usually superior, half-inferior in Sarcobatus, inferior and connate with receptacle in fruit in Beta, 1-locular with single, basally attached ovule. |
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Ovules | usually 1, campylotropous, bitegmic, crassinucellate. |
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Seeds | dimorphic: brown, 2.5–4 mm wide (often the only ones present), or black, (1.2–)1.5–2.9(–3) mm wide; radicle median, ± antrorse, of brown seed basal and spreading. |
1 per flower, black, brown, reddish brown, or mixture, flattened vertically or rounded, margins winged or not winged, surfaces smooth and shiny or reticulate, regulate, verrucate, prickly, or indistinct, morphology variable and strongly influenced by plant photoperiod; seed coat smooth, striate, or verrucate when pericarp is removed; embryo large, curved to annular or spirally coiled; radicle position median or basal, ascending or pointing outward; endosperm usually digested by developing embryo and food storage taken over by perisperm. |
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Bracteoles | green, becoming black or reddish to yellow brown, sessile or some short stipitate, venation obscure, ovate-triangular to rhombic-triangular, 5–13 mm, margin united almost to middle, with few irregular teeth or entire, apex abruptly acuminate, faces irregularly muricate, tuberculate, or smooth, inflated, spongy inner layer strongly developed at bracteole base. |
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Fruiting | structures: bracteoles or fruiting bracts brown, black, or reddish brown, monomorphic or sometimes dimorphic; perianth segments deciduous or persistent in mature fruits and of various shapes and ornamentation, accrescent around fruits; fruits achenes or utricles, vertical or horizontal within perianth parts, pericarp (ovary wall) adherent or nonadherent, chartaceous or papery, sometimes reticulate, mottled or smooth. |
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Polyploidy | common. |
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x | = 9. |
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2n | = 18, 36. |
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Atriplex glabriuscula |
Chenopodiaceae |
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Distribution |
CT; MA; ME; NH; PA; AB; MB; NB; NS; PE; QC; Europe
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Worldwide; especially in desert and semidesert regions; often in alkaline or saline habitats |
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Discussion | Varieties 3 (3 in the flora). Members of the Atriplex glabriuscula complex occupy saline or brackish marshes and saline coastal strands mainly in the eastern maritime provinces of Canada, with extensions in similar habitats into the northeastern United States. They are seldom, if ever, ruderal weeds and appear to be indigenous or perhaps early introduced in some part from similar European habitats. The constituent taxa have been regarded at specific level (P. M. Taschereau 1972; I. J. Bassett et al. 1983). They are, however, alike in all major morphologic features, and are apparently closely allied. For those who wish to treat them at specific level, the names are supplied in the synonymy. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Genera ca. 100, species ca. 1500 (27 genera, 168 species in the flora). A number of species introduced from Europe and Asia are weedy in North America. The widespread distribution of the family in the deserts of Eurasia and Australia is indicative of the ancient status of the family. Fossil pollen from this family dates to the Maestrichtian, providing the oldest known fossils in the Caryophylliidae. Plants in this family typically have Crassulacean Acid Metabolism, have either a C3 or C4 photosynthetic pathway (W. V. Brown 1975; G. W. Welkie and M. Caldwell 1970), accumulate organic acids, free nitrates, and oxalates, and often contain alkaloids. Along with other members of the Caryophyllales, members of the family contain pigments called betalains (named for the genus Beta) rather than anthocyanins. Economically important members of this family include spinach and chard (Spinacia oleracea) and beets (Beta vulgaris). Seeds in this family generally provide a rich source of protein, and one species, Chenopodium quinoa, is gaining widespread acceptance as a cereal crop. Toxicity from high levels of nitrates or oxalates has been reported for a number of species (J. M. Kingsbury 1964), and the pollen is known to be allergenic (T. C. Fuller and E. McClintock 1986). The nutritional characteristics of many species that we share with northern Asia were described by M. M. Iljin (1936). Molecular and morphologic studies provide evidence supporting the inclusion of the Chenopodiaceae within Amaranthaceae (Angiosperm Phylogeny Group 1998; W. S. Judd and I. K. Ferguson 1999; J. E. Rodman 1990). However, until discordant elements within these lineages, such as Sarcobatus (H.-D. Behnke 1997), are interpreted within a larger evolutionary scheme, the disposition of family groups remains problematic. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Source | FNA vol. 4. | FNA vol. 4, p. 258. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | Chenopodiaceae > Atriplex > subg. Atriplex > sect. Teutliopsis | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Name authority | Edmondston: Fl. Shetland, 39. (1845) | Ventenat | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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