Polygonum parryi |
Polygonum aviculare |
|||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Parry's knotweed, Parry's or prickly knotweed, prickly knotweed |
birdweed, common knotgrass, common knotweed, doorweed, dooryard knotweed, knotgrass, knotweed, lowgrass, pigweed, prostrate knotweed, renouée des oiseaux, yard knotweed |
|||||||||||||||||||||||||||||
Habit | Herbs, compact, often cushion-like. | Plants green or bluish green, green after drying, sometimes whitish from powdery mildew, homophyllous or heterophyllous. | ||||||||||||||||||||||||||||
Stems | erect, green-brown, simple or branched from base, not wiry, 2–5(–8) cm, glabrous. |
prostrate to erect, branched, flexuous, 5–200 cm. |
||||||||||||||||||||||||||||
Leaves | ± uniformly distributed, dense, not articulated to ocreae, basal leaves ± persistent, distal leaves gradually reduced to bracts; ocrea 2–4(–5) mm, glabrous, proximal part cylindric, distal part deeply lacerate, disintegrating into white, curled fibers; petiole absent; blade 3-veined, without pleats, linear-lanceolate, subulate, 5–13(–20) × 0.4–1 mm, margins revolute, smooth, apex spine-tipped. |
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. |
||||||||||||||||||||||||||||
Inflorescences | axillary; cymes in most axils, 1-flowered. |
axillary; cymes uniformly distributed or aggregated at tips of stems and branches, 1–6(–8)-flowered. |
||||||||||||||||||||||||||||
Pedicels | absent. |
enclosed in or exserted from ocreae, 1.5–5 mm. |
||||||||||||||||||||||||||||
Flowers | closed; perianth 1.5–2(–2.5) mm; tube 6–15% of perianth length; tepals overlapping, usually reddish with white margins, petaloid, oblong, navicular, apex acute; midveins unbranched; stamens 8. |
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. |
||||||||||||||||||||||||||||
Achenes | slightly exserted from perianth at maturity, dark brown, ovate, 1.2–1.6(–2) mm, faces subequal, shiny, smooth. |
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. |
||||||||||||||||||||||||||||
Polygonum parryi |
Polygonum aviculare |
|||||||||||||||||||||||||||||
Phenology | Flowering May–July. | |||||||||||||||||||||||||||||
Habitat | Vernally moist, open, sandy or rocky places | |||||||||||||||||||||||||||||
Elevation | 500-2000 m (1600-6600 ft) | |||||||||||||||||||||||||||||
Distribution |
CA; WA
|
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
|
||||||||||||||||||||||||||||
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.) |
|||||||||||||||||||||||||||||
Key |
|
|||||||||||||||||||||||||||||
Source | FNA vol. 5, p. 563. | FNA vol. 5, p. 556. | ||||||||||||||||||||||||||||
Parent taxa | Polygonaceae > subfam. Polygonoideae > Polygonum > sect. Duravia | Polygonaceae > subfam. Polygonoideae > Polygonum > sect. Polygonum | ||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||||||||||
Name authority | Greene: Bull. Torrey Bot. Club 8: 99. (1881) | Linnaeus: Sp. Pl. 1: 362. (1753) | ||||||||||||||||||||||||||||
Web links |
|
|