Sarcocornia |
Chenopodiaceae |
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glasswort, pickleweed, saltwort, samphire, swampfire |
goosefoot family |
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Habit | Shrubs, glabrous. | 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 | apparently jointed and fleshy when young, becoming woody and not jointed, not armed; some stems terminated by an inflorescences, others entirely vegetative. |
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 | opposite, united at base, petiolate, decurrent forming fleshy joints (sterile segments) fleshy on stem, fleshy; eventually deciduous; blade fleshy triangular projections at tips of joints, edges with narrow scarious margins. |
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 | terminal and lateral, spikelike, apparently jointed, each joint (fertile segment) consisting of 2 opposite, axillary, 3(–5)-flowered cymes embedded in and adnate to fleshy tissue of distal internode; flowers in each cyme arranged in transverse rows, central flower separating lateral flowers, slightly larger; flowers in each cyme partially separated by flaps of tissue which persist on stem when flowers have fallen. |
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 | bisexual or unisexual, ± radially symmetric; perianth segments persistent in fruit, 3–4, united except at tip, fleshy; stamens 1–2; styles 2–3. |
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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Fruits | utriclelike, ellipsoid; pericarp membranous. |
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Ovules | usually 1, campylotropous, bitegmic, crassinucellate. |
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Seeds | vertical, ellipsoid; seed coat light brown, membranous, pubescent; hairs strongly curved or hooked and slender, or conic, straight or slightly curved; perisperm absent. |
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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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. |
= 9. |
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Sarcocornia |
Chenopodiaceae |
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Distribution |
North America; w Europe; Mediterranean region; s Africa; e Africa; Australasia |
Worldwide; especially in desert and semidesert regions; often in alkaline or saline habitats |
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Discussion | Species ca. 15 (3 in the flora). Sarcocornia is taxonomically difficult and has never been the subject of a taxonomic revision for the Northern Hemisphere. Although it is possible to identify dry specimens to some extent, by comparison, it is impossible to obtain from dried specimens data that can be used in a taxonomic revision. Characters that may be taxonomically useful are lost on drying, especially flower and inflorescence characters and those derived from the fleshy vegetative segments. Habit appears to be useful, but few specimen labels note the habit of the living plant, and the parts collected rarely allow for a reliable determination of habit. Some species, such as S. perennis are prostrate, with the woody stems readily rooting in the substrate. Others such as S. pacifica are procumbent to erect shrubs in which the woody stems usually do not root. This apparently obvious habit difference is sometimes confounded by external factors, erect species becoming procumbent due to water movement, trampling, or burial by silt or sand deposits. Conversely, prostrate rooting species can be disturbed by erosion and appear to be procumbent plants of a nonrooting species. One of the most useful characters, the indumentum on the testa of the seeds, is rarely present in dried specimens because of the lateness of the plants’ flowering season. Plants collected in August and September rarely have even immature seeds present, so most herbarium specimens do not display this character. The consequence of these problems is that most accounts of Sarcocornia in North America recognize only one species, frequently using the name Salicornia virginica Linnaeus for the collective entity. The type specimens of S. virginica were collected by John Clayton, presumably from Virginia, which are immature annuals and not flowering. The name S. virginica cannot be applied to a species in this genus. (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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms | Salicornia section Perennes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | A. J. Scott: B ot. J. Linn. Soc. 75: 366. (1978) | Ventenat | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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