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birdweed, common knotgrass, common knotweed, doorweed, dooryard knotweed, knotgrass, knotweed, lowgrass, pigweed, prostrate knotweed, renouée des oiseaux, yard knotweed

close-flower knotweed, close-flower knotweed (ssp. confertiflorum), Kellogg's knotweed (ssp. kelloggii), milkwort knotweed, polygala knotweed, whitemargin knotweed

Habit Plants green or bluish green, green after drying, sometimes whitish from powdery mildew, homophyllous or heterophyllous. Herbs.
Stems

prostrate to erect, branched, flexuous, 5–200 cm.

erect, green, usually divaricately branched, rarely simple, ± wiry, (2–)6–20(–25) cm, glabrous.

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.

uniformly distributed, articulated to ocreae, basal leaves often caducous, distal leaves abruptly reduced to bracts;

ocrea 4–8 mm, glabrous, proximal part cylindric, distal part silvery, with inconspicuous veins, lacerate;

petiole absent;

blade 3-veined, lateral veins sometimes inconspicuous, without pleats, narrowly linear, 10–40 × 1–2.5 mm, margins ± revolute, smooth, apex acute or mucronate.

Inflorescences

axillary;

cymes uniformly distributed or aggregated at tips of stems and branches, 1–6(–8)-flowered.

axillary and terminal, spikelike, subglobose to cylindric;

cymes in most axils or crowded distally, 1–3-flowered.

Pedicels

enclosed in or exserted from ocreae, 1.5–5 mm.

enclosed in ocreae, erect, 0.1–2 mm, sometimes absent.

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.

mostly closed;

perianth 1.5–3 mm;

tube 19–40% of perianth length;

tepals overlapping, uniformly white, pink, or red, petaloid, oblong-lanceolate, ± navicular, apex acute to acuminate;

midveins usually unbranched or with 2 lateral branches proximally, moderately to strongly thickened, tepals appearing ± keeled;

stamens 3–8.

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.

enclosed in perianth, light yellow, light brown, or greenish brown to dark brown, ovate to lanceolate, 1.3–2.5 mm, faces subequal, shiny or dull, smooth or reticulate with longitudinal ridges.

Polygonum aviculare

Polygonum polygaloides

Distribution
from FNA
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
[WildflowerSearch map]
[BONAP county map]
from FNA
AZ; CA; CO; ID; MT; NM; NV; OR; UT; WA; WY; AB; BC; SK
[WildflowerSearch map]
[BONAP county map]
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 4 (4 in the flora).

J. C. Hickman’s (1993c) treatment of the Polygonum polygaloides complex is provisionally accepted here. Most of the intermediate specimens occur between subspp. confertiflorum, esotericum, and kelloggii. Alternatively, P. polygaloides could be recognized in the narrow sense and the three other taxa could be treated as subspecies of a separate P. kelloggii, the earliest available binomial.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Key
1. Perianth tubes 40-57% of perianth length
→ 2
1. Perianth tubes (15-)20-40(-42)% of perianth length. [3. Shifted to left margin.—Ed.]
→ 3
2. Tepals green or reddish brown, margins white, veins unbranched
subsp. depressum
2. Tepals green, margins usually pink or red, rarely white, veins branched
subsp. neglectum
3. Perianths 3.3-5.5 mm; achenes 2.5-4.2 mm
→ 4
3. Perianths 1.9-3.6 mm; achenes 1.2-2.8(-3) mm
→ 5
4. Plants heterophyllous; leaf blades elliptic to oblanceolate; tepals oblong, cucullate in fruit; cymes aggregated at tips of stems and branchs; broad distribution in North America
subsp. aviculare
4. Plants homophyllous or subheterophyllous; leaf blades obovate-spatulate or oblanceolate; tepals obovate, flat or curved outward in fruit; cymes ± uniformly distributed; Greenland, Newfoundland and Labrador
subsp. boreale
5. Ocreae with distal parts relatively persistent, silvery; perianths 0.9-1.3(-1.5) times as long as wide, outer tepals pouched at base
subsp. buxiforme
5. Ocreae soon disintegrating into persistent fibers or leaving almost no fibrous remains; perianths 1.5-2.9 times as long as wide; outer tepals not pouched at base
→ 6
6. Leaf blades (6-)10-20 mm wide, 2-4.5 times as long as wide; cymes 3-8-flowered, aggregated at tips of stems and branches; achenes enclosed in or barely exserted from perianth
subsp. aviculare
6. Leaf blades 0.5-6.8(-8) mm wide, (3.4-)4.2-15(-19) times as long as wide; cymes 1-3(-5)-flowered, uniformly distributed along stems and branches; achenes usually exserted from perianth
→ 7
7. Ocreae 4-8 mm, veins inconspicuous, distal parts leaving almost no fibrous remains; lateral veins of leaf blades visible but not raised adaxially
subsp. neglectum
7. Ocreae (6-)8-12 mm, veins conspicuous, distal parts disintegrating into persistent fibers; lateral veins of leaf blades raised adaxially
subsp. rurivagum
1. Margins of bracts green, if white then scarious border less than 0.2 mm wide
→ 2
1. Margins of bracts white, scarious border (0.2-)0.25-1 mm wide
→ 3
2. Achenes lanceolate, 2-2.5 mm; bracts elliptic-lanceolate, appressed, rigid; stamens 5-8
subsp. esotericum
2. Achenes ovate, 1.3-1.7 mm; bracts linear to linear-lanceolate, ± patent, soft; stamens 3
subsp. kelloggii
3. Inflorescences narrowly cylindric, continuous from bases of branches or stems; achenes 2-2.5 mm, lanceolate
subsp. esotericum
3. Inflorescences round to ovate or cylindric, confined to tips of branches, rarely continuous from bases of branches or stems; achenes 1.3-2.1 mm, ovate-lanceolate to ovate
→ 4
4. Inflorescences round to ovate; scarious borders of bracts 0.5-1 mm wide; stamens8
subsp. polygaloides
4. Inflorescences ovate to cylindric; scarious borders of bracts 0.25-0.4 mm wide; stamens 3
subsp. confertiflorum
Source FNA vol. 5, p. 556. FNA vol. 5, p. 565.
Parent taxa Polygonaceae > subfam. Polygonoideae > Polygonum > sect. Polygonum Polygonaceae > subfam. Polygonoideae > Polygonum > sect. Duravia
Sibling taxa
P. achoreum, P. argyrocoleon, P. austiniae, P. bidwelliae, P. bolanderi, P. californicum, P. cascadense, P. douglasii, P. engelmannii, P. erectum, P. fowleri, P. glaucum, P. heterosepalum, P. hickmanii, P. humifusum, P. majus, P. marinense, P. minimum, P. nuttallii, P. oxyspermum, P. paronychia, P. parryi, P. patulum, P. plebeium, P. polygaloides, P. ramosissimum, P. sawatchense, P. shastense, P. spergulariiforme, P. striatulum, P. tenue, P. utahense
P. achoreum, P. argyrocoleon, P. austiniae, P. aviculare, P. bidwelliae, P. bolanderi, P. californicum, P. cascadense, P. douglasii, P. engelmannii, P. erectum, P. fowleri, P. glaucum, P. heterosepalum, P. hickmanii, P. humifusum, P. majus, P. marinense, P. minimum, P. nuttallii, P. oxyspermum, P. paronychia, P. parryi, P. patulum, P. plebeium, P. ramosissimum, P. sawatchense, P. shastense, P. spergulariiforme, P. striatulum, P. tenue, P. utahense
Subordinate taxa
P. aviculare subsp. aviculare, P. aviculare subsp. boreale, P. aviculare subsp. buxiforme, P. aviculare subsp. depressum, P. aviculare subsp. neglectum, P. aviculare subsp. rurivagum
P. polygaloides subsp. confertiflorum, P. polygaloides subsp. esotericum, P. polygaloides subsp. kelloggii, P. polygaloides subsp. polygaloides
Name authority Linnaeus: Sp. Pl. 1: 362. (1753) Meisner: in A. P. de Candolle and A. L. P. P. de Candolle, Prodr. 14: 101. (1856)
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