Amaranthus hybridus |
Amaranthaceae |
|||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
green amaranth, green pigweed, hybrid amaranth, slender pigweed, slim amaranth, smooth amaranth, smooth pigweed |
amaranth family |
|||||||||||||||||||||||||||||||||||||||||||||||||||||
Habit | Plants glabrous or glabrescent, or distal parts of stem and branches slightly pubescent when young. | Herbs, rarely subshrubs, annual or perennial; trichomes simple (branched in Tidestromia). | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Stems | erect, green or sometimes reddish purple, rarely under-developed plants ascending, branched to nearly simple, 0.3–2(–2.5) m. |
without nodal spines (Amaranthus spinosus sometimes with paired nodal spines). |
||||||||||||||||||||||||||||||||||||||||||||||||||||
Leaves | petiole 1/2 as long as to equaling blade; blade ovate, rhombic-ovate, or lanceolate, (2–)4–15 × (1–)2–6 cm, base cuneate to broadly cuneate, margins entire, apex acute to obtuse, with mucro. |
alternate or opposite, exstipulate, usually petiolate; blade margins entire (entire or serrulate in Iresine; entire, crispate, or erose in Amaranthus). |
||||||||||||||||||||||||||||||||||||||||||||||||||||
Bracts | lanceolate-linear to subulate, 2–3.5(–4) mm, subequal to or 2 times as long as tepals, apex spinescent. |
|||||||||||||||||||||||||||||||||||||||||||||||||||||
Inflorescences | terminal and axillary, erect or reflexed, occasionally nodding, green or olive green, occasionally with silvery or reddish purple tint, leafless at least distally, terrminal inflorescence often slightly nodding with numerous shorter branches at base. |
cymules arranged in spikes, panicles, thyrses, heads, glomerules, clusters, or racemes; each flower subtended by 1 bract and 2 bracteoles (latter sometimes 1 or absent in Amaranthus). |
||||||||||||||||||||||||||||||||||||||||||||||||||||
Flowers | bisexual or unisexual (plants then monoecious or dioecious), hypogynous, generally small or minute; tepals mostly (1–)4–5 or absent, distinct or connate into cups or tubes, scarious, chartaceous, membranaceous, or indurate; stamens 2–5, filaments basally connate into cups or tubes, rarely distinct, alternating with pseudostaminodes (appendages on staminal tubes) or not, anthers 2-locular with 1 line of dehiscence or 4-locular with 2 lines of dehiscence; ovary superior, 1-locular; ovules 1 or, rarely, 2–many; style 1 or absent; stigmas 1–3(–5). |
|||||||||||||||||||||||||||||||||||||||||||||||||||||
Staminate flowers | at tips of inflorescences; tepals 5; stamens (4–)5. |
|||||||||||||||||||||||||||||||||||||||||||||||||||||
Pistillate flowers | tepals 5, lanceolate to lanceolate-linear, subequal or unequal, 1.5–3 mm, membranaceous, apex acute or acuminate, gradually narrowing into aristate tip; style branches erect, shorter than body of fruit; stigmas 3. |
|||||||||||||||||||||||||||||||||||||||||||||||||||||
Fruits | utricles, dry, dehiscent or not. |
|||||||||||||||||||||||||||||||||||||||||||||||||||||
Seeds | black to dark reddish brown, lenticular to lenticular-globose, 1–1.3 mm, smooth, shiny. |
black, reddish brown, or brown, lenticular, subglobose or globose (rarely cylindric), usually small; embryo peripheral, surrounding mealy perisperm. |
||||||||||||||||||||||||||||||||||||||||||||||||||||
Utricles | obovoid or elongate-ovoid, 1.5–2.5 mm, shorter than tepals, smooth proximally, lid verrucose or rugose, dehiscence regularly circumscissile, or rarely in some presumably hybrid forms, irregularly dehiscent or indehiscent. |
|||||||||||||||||||||||||||||||||||||||||||||||||||||
Amaranthus hybridus |
Amaranthaceae |
|||||||||||||||||||||||||||||||||||||||||||||||||||||
Phenology | Flowering summer–fall. | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Habitat | Waste places, agricultural and fallow fields, railroads, roadsides, riverbanks, other disturbed habitats | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Elevation | 0-2500 m (0-8200 ft) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Distribution |
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; PA; RI; SC; SD; TN; TX; VA; VT; WA; WI; WV; BC; MB; NS; ON; QC; Mexico; Central America; South America; West Indies [Widely introduced or naturalized in tropical, subtropical, and warm-temperate regions worldwide]
|
Nearly worldwide; most abundant in tropics; subtropics; and warm-temperate regions; evidently absent from alpine and arctic regions |
||||||||||||||||||||||||||||||||||||||||||||||||||||
Discussion | Originally a riverside pioneer in eastern North America, now Amaranthus hybridus is extremely abundant in agricultural fields and other disturbed habitats. Related cultivated species have been reported from the flora area, including A. caudatus, A. hypochondriacus, and A. cruentus; there is no evidence that they are established; specimens identified as these species are often variants of A. hybridus. Distribution of Amaranthus hybridus in North America needs clarification because the name was misapplied to other species, notably A. powellii, and specimens of A. retroflexus, A. powellii, and A. hybridus are frequently interchangeably misidentified. Forms of A. hybridus and A. powellii with reddish inflorescences are often misidentified as escaped and hence presumably naturalized, cultivated species A. caudatus Linnaeus, A. hypochondriacus Linnaeus, and A. cruentus Linnaeus. Amaranthus hybridus is extremely variable. In particular, there are numerous North American specimens with subobtuse tepals and thick inflorescences, suggesting hybridization with A. retroflexus. In Europe such presumably hybrid forms are known as A. ×ozanonii Thellung (A. Thellung 1914–1919). A new, presumably hybridogenous taxon, Amaranthus ×tucsonensis Henrickson, was recently described from Arizona (J. Henrickson 1999). It was suggested that one of its parents is A. hybridus; the other parental species (probably a species with obtuse or spatulate tepals) remains unknown. The problem of proper taxonomic position and origin of A. ×tucsonensis needs further study. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Genera ca. 65, species ca. 900 (12 genera, 80 species in the flora). Centers of diversity for Amaranthaceae are southwestern North America, Central America, South America, and Africa south of the Sahara Desert. Generic limits are not well defined in some groups; fewer than 60 or more than 70 genera could be recognized. Some species occur in severe habitats such as sandy, calcareous, gypseous, saline, or serpentine soils in deserts, semideserts, and seashores. Some species are weedy, including the major agricultural weeds in Amaranthus. Some species are cultivated as ornamentals, particularly Amaranthus caudatus (love-lies-bleeding), A. hypochondriacus (prince’s-feather), A. tricolor (Joseph’s-coat), Celosia cristata (cockscomb), and Gomphrena globosa (globe-amaranth). Native Americans domesticated white-seeded grain amaranths (A. caudatus, A. cruentus, and A. hypochondriacus) for use as cereal grains. Some species of Amaranthus and Celosia are potherbs. Amaranthaceae are usually divided into subfamilies Amaranthoideae (anthers 4-locular with two lines of dehiscence) and Gomphrenoideae Schinz (anthers 2-locular with one line of dehiscence). Amaranthaceae and Chenopodiaceae have long been recognized as allied families that share a number of features: generally small flowers, one perianth whorl, a syncarpous gynoecium with a superior ovary and often only one ovule, basal or free-central placentation, pollen characteristics, centrospermous embryo development, betalain pigments, and P-type form (c) sieve-element plastids. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
||||||||||||||||||||||||||||||||||||||||||||||||||||
Key |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||
Source | FNA vol. 4. | FNA vol. 4, p. 405. | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | Amaranthaceae > Amaranthus > subg. Amaranthus | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | Linnaeus: Sp. Pl. 2: 990. (1753) | Jussieu | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Web links |
|
|