Amaranthus retroflexus |
Amaranthus hypochondriacus |
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common amaranth, pigweed amaranth, red-root amaranth, red-root pigweed, rough pigweed, wild-beet amaranth |
amaranthus hypochondriacus, Prince's-feather, Prince's-feather amarant h, Prince-of-Wales-feather |
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Habit | Plants densely to moderately pubescent, especially distal parts of stem and branches. | Plants glabrous or moderately pubescent in distal parts, often becoming glabrescent at maturity. |
Stems | erect, reddish near base, branched in distal part to simple 0.2–1.5(–2) m; underdeveloped or damaged plants rarely ascending to nearly prostrate. |
usually erect, green or reddish purple, branched, mainly in inflorescences, to nearly simple proximally, 0.4–2(–2.5) m, coarse. |
Leaves | petiole 1/2 to equaling blade; blade ovate to rhombic-ovate, 2–15 × 1–7 cm, base cuneate to rounded-cuneate, margins entire, plane or slightly undulate, apex acute, obtuse, or slightly emarginate, with terminal mucro. |
petiole of distal leaves equaling or slightly shorter than blade, becoming longer proximally; blade rhombic-ovate to broadly lanceolate 4–12 × 2–7 cm, larger in robust plants, base cuneate to broadly cuneate, narrowly cuneate in distal leaves, margins entire, apex cuneate to obtuse or indistinctly emarginate, mucronulate. |
Bracts | lanceolate to subulate, (2.5–)3.5–5(–6) mm, exceeding tepals, apex acuminate with excurrent midrib. |
lanceolate to linear-subulate, subspinescent, 3–6(–8) mm, to 2 times as long as tepals, rigid. |
Inflorescences | terminal and axillary, erect or reflexed at tip, green or silvery green, often with reddish or yellowish tint, branched, leafless at least distally, usually short and thick. |
predominantly terminal, often with few spikes at distal axils stiff, erect, dark red, purple, or deep beet-red, less commonly yellowish or greenish, leafless at least in distal part, usually robust. |
Staminate flowers | few at tips of inflorescences; tepals 5; stamens (3–)4–5. |
clustered at tips of inflorescence branches; tepals 3–5; stamens 3–5. |
Pistillate flowers | tepals 5, spatulate-obovate, lanceolate-spatulate, not clawed, subequal or unequal, (2–)2.5–3.5(–4) mm, membranaceous, apex emarginate or obtuse, with mucro; style branches erect or slightly spreading,; stigmas 3. |
tepals usually 5, proximal ones lanceolate, distal ones narrowly ovate-elliptic to elliptic, not clawed, unequal to occasionally subequal, 1.3–3(–3.5) mm, apex acute; style branches spreading; stigmas 3. |
Seeds | black to dark reddish brown, lenticular to subglobose-lenticular, 1–1.3 mm, smooth, shiny. |
white, ivory, pinkish white, or black to dark reddish brown, subglobose to lenticular, 1–1.4 mm diam., smooth, shiny. |
Utricles | broadly obovoid to broadly elliptic, 1.5–2.5 mm, shorter than or subequal to tepals, smooth or slightly rugose, especially near base and in distal part, dehiscence regularly circumscissile. |
compressed-ovoid to elongate-ovoid, (1.5–)2–3 mm, equaling tepals or nearly so, smooth or lid slightly rugose or minutely verrucose, dehiscence regularly circumscissile. |
Amaranthus retroflexus |
Amaranthus hypochondriacus |
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Phenology | Flowering summer–fall. | Flowering summer–fall. |
Habitat | Banks of rivers, lakes, and streams, disturbed habitats, agricultural fields, railroads, roadsides, waste areas | Near places of cultivation |
Elevation | 0-2500 m (0-8200 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; NU; ON; PE; QC; SK; SPM [Introduced and naturalized nearly worldwide]
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AZ; MA; MI; NE; NM; NY; TX; UT; WI; WV; cultivated widely |
Discussion | Amaranthus retroflexus, native to central and eastern North America, is a successful invasive species and has effectively colonized a wide range of habitats on all inhabited continents. Its variability is extremely wide; usually the species is easily recognized and its identification causes no specific problems. Infraspecific entities described within A. retroflexus are mostly ecologic variants of little or no taxonomic value. Two varieties are more easily recognized: the common var. retroflexus, with bracts about 1.5–2 times as long as tepals, and a more rare var. delilei (Richter & Loret) Thellung (= A. delilei Richter & Loret), with bracts 1–1.5 times as long as tepals. Occasional forms morphologically intermediate between Amaranthus retroflexus and taxa of the A. hybridus aggregate (e.g., A. powellii and A. hybridus, in the strict sense) are known both in the Americas and the Old World. Usually such plants are treated as hybrids; in many cases they are probably just extremes of the natural variability of A. retroflexus. Putative hybrids of A. retroflexus were described from Europe as A. ×ozanonii Thellung (A. hybridus × A. retroflexus) and A. ×soproniensis Priszter & Karpáti (A. powellii × A. retroflexus) (see A. Thellung 1914–1919; S. Priszter 1958; P. Aellen 1959; F. Grüll and S. Priszter 1973). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Amaranthus hypochondriacus and its hybrids are widely cultivated as ornamental, pseudocereal, and fodder crops in many tropical to warm-temperate regions of the world. Occasionally, A. hypochondriacus occurs as escapes near the places of cultivation; there are no reliable reports of its successful naturalization in the flora area. The wild progenitor of Amaranthus hypochondriacus seems to be A. powellii (J. D. Sauer 1967b); hybridization with other cultivated taxa (e.g., A. cruentus) probably also played some role. The initial cultivated form probably emerged in southwestern North America, within the original range of native A. powellii. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 4. | FNA vol. 4. |
Parent taxa | Amaranthaceae > Amaranthus > subg. Amaranthus | Amaranthaceae > Amaranthus > subg. Amaranthus |
Sibling taxa | ||
Synonyms | A. retroflexus var. salicifolius | |
Name authority | Linnaeus: Sp. Pl. 2: 991. (1753) | Linnaeus: Sp. Pl. 2: 991. (1753) |
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