Polygonum argyrocoleon |
Polygonum douglasii |
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Persian knotweed, silver sheath knotweed |
Douglas' knotweed, renouée de Douglas |
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Habit | Plants green, heterophyllous. | Herbs. |
Stems | erect or decumbent, branched mostly from base, not wiry, 15–100 cm. |
erect, green, simple or branched, not wiry, 5–80 cm, glabrous or sparsely papillose-scabridulous. |
Leaves | ocrea 4–8 mm, proximal part cylindric, distal part soon disintegrating into curly or straight fibers; petiole 0–1.5 mm; blade bluish green, lanceolate or linear-lanceolate, 15–50 × 2–8 mm, margins flat, apex acute; stem leaves 2.1–4 times as long as branch leaves; distal leaves abruptly reduced and not overtopping flowers (shorter than or equaling flowers). |
uniformly distributed, articulated to ocreae, basal leaves caducous, distal leaves abruptly reduced to bracts; ocrea 6–12 mm, glabrous or minutely papillose-scabridulous, proximal part cylindric, distal part hyaline, lacerate; petiole 0.1–2 mm; blade 1-veined, not pleated, linear, narrow-oblong, or oblanceolate, 15–55 × 2–8(–12) mm, margins revolute, smooth or papillose-denticulate; apex acute to mucronate. |
Inflorescence(s) | axillary and terminal, spikelike; cymes aggregated at tips of stems and branches, 4–6-flowered, bracts inconspicuous. |
axillary and terminal, spikelike, elongate; cymes widely spaced along branches, 2–4-flowered. |
Pedicels | enclosed in ocreae, 1–2 mm. |
mostly exserted from ocreae, reflexed, 2–6 mm. |
Flowers | closed; perianth 1.8–2.4 mm; tube 10–22% of perianth length; tepals overlapping, green or white, usually with pink, rarely red or white, margins, petaloid, not keeled, oblong to obovate, cucullate; midveins usually unbranched; stamens 7–8. |
closed; perianth 3–4.5 mm; tube 20–28% of perianth length; tepals overlapping, green to tannish with white or pink margins, petaloid, oblong, cucullate, navicular, apex rounded; midveins usually branched, rarely unbranched; stamens 8. |
Achenes | enclosed in perianth, brown, ovate, 3-gonous, 1.3–2.3 mm, faces subequal, slightly concave, apex not beaked, with concave edges, shiny, smooth; late-season achenes unknown. |
enclosed in perianth, black, elliptic or oblong to ovate, 3–4(–4.5) mm, faces subequal, shiny or dull, smooth or minutely striate-tubercled. |
Polygonum argyrocoleon |
Polygonum douglasii |
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Phenology | Flowering May–Oct. | Flowering Jun–Oct. |
Habitat | Fields, gardens, disturbed sites, often in saline soils | Dry, often disturbed places, rock outcrops, sandy ground |
Elevation | 0-1200 m (0-3900 ft) | 300-3000 m (1000-9800 ft) |
Distribution |
AZ; CA; CO; FL; ID; LA; MA; MO; NC; NM; NV; TX; UT; VT; WV; c Asia [Introduced in North America]
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AZ; CA; CO; IA; ID; MI; MN; MT; NE; NH; NM; NV; NY; OR; SD; UT; VA; VT; WA; WY; AB; BC; MB; ON; QC; SK; YT
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Discussion | Five taxa that have been included in Polygonum douglasii (E. Murray 1982; J. C. Hickman 1984; J. T. Kartesz and K. N. Gandhi 1990) are treated here as distinct species: P. austiniae, P. majus, P. nuttallii, P. sawatchense, and P. spergulariiforme. Hickman noted extensive intergradation and numerous intermediate specimens among those sympatric elements, but qualitative or quantitative characters allow reliable discrimination in most cases (M. Costea and F. J. Tardif 2005), and species are here circumscribed similar to C. L. Hitchcock (1964). Greene described var. latifolium as having leaf blades and achenes broader than those of var. douglasii. C. L. Hitchcock (1964) recognized the former, but the characters used to distinguish it appear to vary continuously, and reliable separation is not possible. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Source | FNA vol. 5, p. 560. | FNA vol. 5, p. 567. |
Parent taxa | Polygonaceae > subfam. Polygonoideae > Polygonum > sect. Polygonum | Polygonaceae > subfam. Polygonoideae > Polygonum > sect. Duravia |
Sibling taxa | ||
Synonyms | P. douglasii var. latifolium, P. emaciatum, P. montanum, P. tenue var. commune, P. tenue var. latifolium | |
Name authority | Steudel ex Kunze: Linnaea 20: 17. (1847) | Greene: Bull. Calif. Acad. Sci. 1: 125. (1885) |
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