Polygonum aviculare |
Polygonum aviculare subsp. neglectum |
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birdweed, common knotgrass, common knotweed, doorweed, dooryard knotweed, knotgrass, knotweed, lowgrass, pigweed, prostrate knotweed, renouée des oiseaux, yard knotweed |
narrow-leaf knotweed, prostrate knotweed, renouée négligée |
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Habit | Plants green or bluish green, green after drying, sometimes whitish from powdery mildew, homophyllous or heterophyllous. | Plants green, homophyllous or sometimes heterophyllous. | ||||||||||||||||||||||||||||
Stems | prostrate to erect, branched, flexuous, 5–200 cm. |
usually 1–7, procumbent to ascending, sometimes erect, mostly branched from base, (5–)15–60 cm. |
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Leaves | ocrea 3–15 mm, proximal part cylindric or ± funnelform, distal part silvery, hyaline, soon disintegrating into persistent fibers or nearly completely deciduous; petiole 0.3–9 mm; blade green to gray-green, narrowly elliptic, lanceolate, elliptic, obovate, or spatulate, 6–50(–60) × 0.5–22 mm, margins flat, apex acute, obtuse, or rounded; stem leaves 1–4 times as long as adjacent branch leaves; distal leaves overtopping flowers. |
ocrea (3–)4–8 mm, proximal part cylindric, distal part with inconspicuous veins, eventually disintegrating and leaving few or no fibrous remains; petiole (0.3–)1–3(–5.2) mm; blade green, lateral veins visible but not raised abaxially, narrowly elliptic or oblanceolate, (7.6–)12.2–34(–40) × 1.5–6.8(–8) mm, (3.4–)4.2–9.2 times as long as wide, apex acute or obtuse; stem leaves 1–2.7(–3.3) times as long as branch leaves. |
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Inflorescences | axillary; cymes uniformly distributed or aggregated at tips of stems and branches, 1–6(–8)-flowered. |
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Pedicels | enclosed in or exserted from ocreae, 1.5–5 mm. |
mostly enclosed in ocreae, 1.5–3 mm. |
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Flowers | closed or semi-open; perianth 1.8–5.5 mm; tube 20–57% of perianth length; tepals overlapping or not, green or reddish brown with white, pink, or red margins, petaloid, not keeled, oblong to obovate, often cucullate in fruit; midveins branched or unbranched, thickened or not; stamens 5–8. |
perianth (1.9–)2.3–3.4 mm, 1.6–2.6 times as long as wide; tube 28–48% of perianth length; tepals overlapping, spreading slightly as achene matures, green usually with pink or red, rarely white, margins, oblong, ± cucullate, outer tepals not pouched at base; veins branched, moderately to strongly thickened; stamens 7–8. |
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Achenes | enclosed in or exserted from perianth, light to dark brown, ovate, (2–)3-gonous, 1.2–4.2 mm, faces subequal or unequal, apex not beaked, edges slightly concave, dull, usually coarsely striate-tubercled, sometimes obscurely tubercled; late-season achenes common or not, 2–5 mm. |
exserted from perianth, dark brown, ovate, 3-gonous, 1.2–1.8 mm, faces unequal or, less often, subequal, flat to concave, apex with straight edges or somewhat bent toward narrow face, striate-tubercled or, rarely, obscurely so; late-season achenes uncommon, 2–3.7 mm. |
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Cymes | uniformly distributed along stems and branches, 1–3(–5)-flowered. |
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2n | = 40, 60. |
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Polygonum aviculare |
Polygonum aviculare subsp. neglectum |
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Phenology | Flowering Jun–Nov. | |||||||||||||||||||||||||||||
Habitat | Disturbed places | |||||||||||||||||||||||||||||
Elevation | 0-1500 m (0-4900 ft) | |||||||||||||||||||||||||||||
Distribution |
AK; AL; AR; AZ; CA; CO; CT; DC; DE; FL; GA; IA; ID; IL; IN; KS; KY; LA; MA; MD; ME; MI; MN; MO; MS; MT; NC; ND; NE; NH; NJ; NM; NV; NY; OH; OK; OR; PA; RI; SC; SD; TN; TX; UT; VA; VT; WA; WI; WV; WY; AB; BC; MB; NB; NL; NS; NT; ON; PE; QC; SK; YT; nearly worldwide
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AK; AL; AR; AZ; CA; CT; GA; IL; IN; KS; KY; LA; MA; MD; ME; MI; MN; MO; MS; MT; NC; ND; NE; NH; NJ; NM; NV; NY; OH; OK; OR; PA; RI; SC; SD; TN; TX; UT; VA; VT; WA; WV; WY; AB; BC; MB; NB; NF; NS; ON; PE; QC; SK; Europe [Introduced in North America] |
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Discussion | Subspecies 7+ (6 in the flora). Polygonum aviculare is a taxonomically controversial polyploid complex of selfing annuals. Although members of the complex have been considered inbreeders, they possess some structures that make cross pollination possible. Cleistogamous and chasmogamous flowers, heterostyly, protandry, and the capacity to secrete nectar suggest an ancestral mixed-mating system. Isoenzyme studies showed that the complex has an allopolyploid origin (P. Meerts et al. 1998) and has evolved as a swarm of inbreeding lines (“Jordanons”) (J. Gasquez et al. 1978). The six subspecies included here have been treated variously (T. Karlsson 2000; M. Costea and F. J. Tardif 2003). Complex intergradation patterns among them make their recognition at the species level impractical. Multivariate analysis and isoenzyme studies show that populations with intermediate characteristics may occur (Meerts et al. 1990, 1998). Except for subsp. boreale, which occurs in Greenland and Labrador, all subspecies are partially sympatric and their distributions have been influenced greatly by humans. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Subspecies neglectum has been reported from Colorado, Idaho, Iowa, and Wisconsin; those reports have not been confirmed. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 5, p. 556. | FNA vol. 5, p. 558. | ||||||||||||||||||||||||||||
Parent taxa | Polygonaceae > subfam. Polygonoideae > Polygonum > sect. Polygonum | Polygonaceae > subfam. Polygonoideae > Polygonum > sect. Polygonum > Polygonum aviculare | ||||||||||||||||||||||||||||
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Synonyms | P. neglectum, P. aequale subsp. oedocarpum, P. aviculare subsp. rectum | |||||||||||||||||||||||||||||
Name authority | Linnaeus: Sp. Pl. 1: 362. (1753) | (Besser) Arcangeli: Comp. Fl. Ital., 583. (1882) | ||||||||||||||||||||||||||||
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