Cerastium alpinum |
Cerastium |
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alpine chickweed, alpine mouse-ear chickweed, céraiste alpin |
cerastium, chickweed, céraiste, mouse-ear chickweed |
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Habit | Plants perennial, mat-forming, rhizomatous. | Herbs, annual, winter annual, or perennial. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Taproots | slender, perennial taxa often rhizomatous, rooting at nodes. |
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Stems | prostrate or ascending, tomentose (very rarely subglabrous), hairs white, translucent, long, soft, flexuous, some usually also short and glandular; flowering shoots ascending, 5–20 cm; small axillary tufts of leaves usually absent; nonflowering shoots ± prostrate, to 6 cm. |
ascending to erect or decumbent, simple or branched, terete. |
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Leaves | marcescent or not, sessile; blade obovate or ovate to elliptic-oblanceolate, elliptic, or lanceolate, usually 10–18 × 5–7 mm, apex obtuse, pubescence as on stems. |
basally connate, petiolate (basal in some species) or sessile (cauline); blade 1–5-veined, linear or elliptic to broadly ovate, not succulent (except in C. bialynickii, C. regelii, and C. viride), apex acute to obtuse. |
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Inflorescences | open, (1–)2–4-flowered cymes; bracts lanceolate, acute, margins narrow, scarious, glandular-pubescent. |
terminal, open or congested cymes, or flowers solitary, axillary (racemosely arranged in C. axillare); bracts paired, foliaceous or reduced, herbaceous or often with scarious margins. |
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Pedicels | straight but often becoming angled at base and curved at apex, slender, 5–30 mm, often elongating to 3 or 4 times as long as sepals, pubescence usually dense, hairs both long, flexuous, multicellular, and short, glandular, viscid. |
erect, sometimes reflexed or hooked at apex in fruit, or flowers sometimes subsessile (C. regelii). |
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Flowers | sepals green, often violet tipped, narrowly elliptic-lanceolate, 7.5–10 mm, margins ± narrow, apex acute to obtuse, densely pubescent, hairs both long, eglandular and short, glandular; petals 1–2 times as long as sepals, apex shallowly 2-fid; stamens 10; styles 5. |
bisexual, occasionally unisexual and pistillate; perianth and androecium hypogynous or weakly perigynous; hypanthium minimal; sepals (4–)5, distinct, green (red-tipped in C. glomeratum and C. pumilum, often violet-tipped in C. alpinum, purple in C. bialynickii, turning pale orange-brown in fruit in C. texanum), elliptic to ovate, 3–12 mm, herbaceous, margins translucent to purplish, scarious, apex acute, acuminate, or obtuse, not hooded; petals (4–)5 or sometimes absent, white (purple tinged in C. pumilum and C. regelii), clawed, blade apex 2-fid 1/5–1/2 of length, notched, or emarginate; nectaries at base of filaments opposite sepals; stamens usually 10, sometimes 5 or 8, occasionally 4; filaments distinct, inserted at base of ovary; staminodes absent or 1–4 (via anther abortion), linear; styles (3–)5(–6), clavate to filiform, 0.5–2 mm, glabrous proximally; stigmas (3–)5(–6), subterminal to linear along adaxial surface of styles, roughened to papillate (30x). |
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Capsules | cylindric, slightly curved, 12–16 mm, to 2 times as long as sepals; teeth 10, erect, margins convolute. |
oblong or cylindric, usually ± curved, opening by 10, or occasionally 6 or 8, erect or spreading, convolute or revolute teeth, longer than sepals; carpophore absent. |
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Seeds | dark brown, 1–1.4 mm diam., acutely tuberculate; testa not inflated. |
15–150+, orange to brown, angular-obovate, often with abaxial groove, laterally compressed, papillate-tuberculate, marginal wing absent, appendage absent. |
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x | = [9?, 13, 15] 17, 18, 19. |
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2n | = 72, 108. |
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Cerastium alpinum |
Cerastium |
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Distribution |
MB; NT; NU; ON; QC; SK; Canada; Greenland; Europe (Iceland, Scandinavia)
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Worldwide; but mainly north-temperate region |
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Discussion | Subspecies 3+ (2 in the flora). The Cerastium alpinum group of species is a difficult complex of intergrading taxa. E. Hultén (1956) considered this complex to be the result of worldwide introgression among the various taxa. Members of this group in North America include C. aleuticum, C. alpinum, C. arcticum, C. beeringianum, C. bialynickii, C. fischerianum, C. regelii, and C. terrae-novae. Cerastium alpinum itself is distinguished from all other members of the complex by its lanate pubescence, which consists of long, silvery, translucent, multicellular, flexuous, often tangled hairs; the more or less square base of the calyx; the convex margins of the sepals; and, in well-grown plants, the long, slender, divaricate pedicels. In western North America, Cerastium alpinum is replaced by C. beeringianum, which has long, straight, strigose, somewhat fuscous hairs, usually smaller flowers, and smaller seeds. The two species intergrade in eastern Canada; intermediate specimens were named C. alpinum var. strigosum Hultén. Cerastium arcticum differs from C. alpinum, with which it often grows, in its straight, somewhat fuscous hairs; calyx which is round at the base; long, narrowly lanceolate sepals; large, straight, broad capsules; and broad, obtuse cauline leaves. Like C. alpinum, it usually has large flowers with the petals much longer than the sepals. Many infraspecific taxa have been named in Cerastium alpinum but in North America it is much less variable than elsewhere. Two forms can be recognized at either the varietal or subspecific level. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Species ca. 100 (27 in the flora). Two names that appear in many North American treatments, Cerastium viscosum Linnaeus and C. vulgatum Linnaeus, have been proposed for rejection (N. J. Turland and M. Wyse Jackson 1997) because they have been a long-standing source of confusion. American authors have frequently applied C. viscosum to C. glomeratum Thuillier but most of the possible lectotypes are referable to C. fontanum. Similarly C. vulgatum has been used for C. fontanum Baumgarten. However the possible lectotypes of C. vulgatum are mixed and most are referable to C. arvense, C. fontanum, and C. glomeratum. I have not attempted to present an infrageneric classification for Cerastium. Several species groupings can be recognized based on capsule structure. Examples include species with the capsule teeth revolute (coiled outwards like a watch spring), e.g., C. maximum and C. texanum, whereas in most of our species the teeth are erect with their margins outwardly rolled (convolute). Also C. cerastoides is anomalous in having three styles, a straight ovoid-conic capsule, and deeply bilobed petals—characters that have led some authors to place it in the genus Stellaria. Accepting the most recent infrageneric classification (B. K. Schischkin 1936), even with subsequent modifications, does not appear to be warranted. Additional study is needed to determine relevant species relationships within the genus. While the base chromosome number for Cerastium is often cited as x = 9, only a single count of 2n = 18 is known; see C. Favarger and M. Krähenbühl (1996) for a discussion of the diverse cytological conditions found in Cerastium. Excluded species: Cerastium clawsonii Correll, described from Texas, is a synonym of Linum hudsonioides Planchet (R. L. Hartman 1979). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Source | FNA vol. 5, p. 77. | FNA vol. 5, p. 74. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | Caryophyllaceae > subfam. Alsinoideae > Cerastium | Caryophyllaceae > subfam. Alsinoideae | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Name authority | Linnaeus: Sp. Pl. 1: 438. (1753) | Linnaeus: Sp. Pl. 1: 437. (1753): Gen. Pl. ed. 5. 199. (1754) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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