Corispermum pacificum |
Chenopodiaceae |
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common bugseed, Pacific bug-seed |
goosefoot family |
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Habit | Plants usually branched from base, (5–)15–40 cm, glabrous or sparsely covered with dendroid hairs (especially when young). | 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 | 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 | blades narrowly lanceolate, linear-lanceolate, or linear, flat or nearly so, 2–5(–7) × 0.2–0.6 cm. |
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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Bracts | ovate-lanceolate, narrowly ovate-lanceolate, almost ovate, or lanceolate, (1–)1.5–2.5 × 0.3–0.7(–0.9) cm. |
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Inflorescences | usually compact, rather dense, or sometimes ± lax, condensed only near apex, ovoid, oblong-ovate, obovate, broadly linear, or occasionally clavate. |
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, 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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Perianth | segment 1, sometimes absent in distal flowers. |
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Fruits | usually black (rarely deep olive green, especially when immature), sharply contrasting with greenish semitransparent wings, without spots and warts, slightly convex abaxially, flat or slightly concave adaxially, orbiculate-obovate to almost orbiculate, broadest near middle (or occasionally slightly beyond), 3–4 × 2.7–3.8 mm, shiny; wing translucent, thin, (0.2–)0.3–0.6 mm wide, margins slightly undulate or indistinctly erose-denticulate, apex rounded or occasionally indistinctly notched. |
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Ovules | usually 1, campylotropous, bitegmic, crassinucellate. |
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Seeds | 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. |
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Corispermum pacificum |
Chenopodiaceae |
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Phenology | Flowering late summer–fall. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Habitat | Sandy shores, dunes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Elevation | 0-500 m (0-1600 ft) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Distribution |
ID; OR; WA
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Worldwide; especially in desert and semidesert regions; often in alkaline or saline habitats |
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Discussion | Of conservation concern. Corispermum pacificum seems to be closely related to Siberian C. crassifolium Turczaninov and C. maynense Ignatov. The latter species occurs in the northeastern Russian Far East and may be expected to occur in Alaska. Corispermum pacificum differs from C. maynense by its usually more robust habit, and its wing rounded (rarely rounded-truncate or indistinctly emarginate, but not triangular) at apex. From C. crassifolium it may be distinguished by the constant presence of perianth segments, and more flattened black mature fruits. Corispermum pacificum probably also occurs in adjacent regions of British Columbia. Corispermum pacificum is placed in subsect. Crassifolia (S. L. Mosyakin 1997). This subsection seems to be of Siberian origin, with its central species, C. crassifolium, being closest to the hypothetic ancestral taxon. The presence of perianth segments in C. pacificum may be explained by ancient hybridization with representatives of subsect. Pallasiana. Reproductive isolation between the sympatric species of Corispermum may be achieved by different flowering periods. Occasional hybrids between C. pacificum and C. villosum are similar in their habit to C. pacificum in having usually broad leaves and rather dense inflorescences but they have mostly aborted fruits suggesting that C. pacificum and C. villosum are taxonomically distant species. (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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Key |
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Source | FNA vol. 4, p. 319. | FNA vol. 4, p. 258. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | Chenopodiaceae > Corispermum | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Name authority | Mosyakin: Novon 5: 345, fig. 1A. (1995) | Ventenat | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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