Amaranthus torreyi |
Amaranthus spinosus |
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Bigelow's amaranth, sandhill amaranth, Torrey's amaranth, Torrey's amaranthus |
spiny amaranth, thorny amaranth |
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Habit | Plants glabrescent to sparsely pubescent. | Plants glabrous or sparsely pubescent in the distal younger parts of stems and branches. |
Stems | erect or ascending proximally, much-branched especially near base, 0.1–0.7 m. Leaves: petiole less than 1/2 as long as blade; blade oblanceolate or lanceolate to ovate-lanceolate, (1.2–)1.5–5(–7) × 0.3–2 cm, base narrowly cuneate to cuneate, margins entire, plane or slightly undulate, apex acute to subobtuse, mucronulate. |
erect or sometimes ascending proximally, much-branched and bushy, rarely nearly simple, 0.3–1(–2) m; each node with paired, divergent spines (modified bracts) to 1.5(–2.5) cm. |
Leaves | petiole ± equaling or longer than blade; blade rhombic-ovate, ovate, or ovate-lanceolate, 3–10(–15) × 1.5–6 cm, base broadly cuneate, margins entire, plane or slightly undulate, apex acute or subobtuse to indistinctly emarginate, mucronulate. |
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Bracts | lanceolate to linear-subulate, 1.3–3.5 mm, slightly longer than tepals. |
of pistillate flowers lanceolate to ovate-lanceolate, shorter than tepals, apex attenuate. |
Inflorescences | axillary clusters, toward apex aggregated in spikes (rarely spicate panicles), axes, leafy (occasionally almost leafless distally). |
simple or compound terminal staminate spikes and axillary subglobose mostly pistillate clusters, erect or with reflexed or nodding tips, usually green to silvery green. |
Staminate flowers | mostly at tips of inflorescences; tepals 5, equal or subequal; stamens 3(–5). |
often terminal or in proximal glomerules; tepals 5, equal or subequal, 1.7–2.5 mm; stamens 5. |
Pistillate flowers | tepals 5, spatulate to narrowly spatulate, clawed, equal or subequal, 1.5–2.5 mm, margins entire, apex obtuse, rounded, or slightly emarginate; style branches erect; stigmas 3. |
tepals 5, obovate-lanceolate or spatulate-lanceolate, equal or subequal, 1.2–2 mm, apex mucronate or short-aristate; styles erect or spreading; stigmas 3. |
Seeds | black, subglobose to broadly lenticular, 1 mm diam., smooth, shiny. |
black, lenticular or subglobose-lenticular, 0.7–1 mm diam., smooth, shiny. |
Utricles | obovoid to subglobose-obovoid, 1.5–2 mm, nearly equaling or slightly shorter than tepals, smooth, dehiscence regularly circumscissile. |
ovoid to subglobose, 1.5–2.5 mm, membranaceous proximally, wrinkled and spongy or inflated distally, irregularly dehiscent or indehiscent. |
Amaranthus torreyi |
Amaranthus spinosus |
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Phenology | Flowering summer–fall. | Flowering summer–fall. |
Habitat | Sandy, rocky, and gravelly flats, slopes, canyons, washes, other naturally disturbed habitats | Waste places, fields, roadsides, railroads, barnyards, overgrazed pastures, other disturbed habitats |
Elevation | 1000-1700 m (3300-5600 ft) | 0-700 m (0-2300 ft) |
Distribution |
AZ; CA; NM; TX; Mexico
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AL; AR; CA; CT; DC; DE; FL; GA; IA; IL; IN; KS; KY; LA; MA; MD; ME; MN; MO; MS; NC; NE; NJ; NY; OH; OK; PA; RI; SC; TN; TX; VA; VT; WI; WV; MB; ON; Mexico; Central America; South America; West Indies [Introduced in North America; introduced nearly worldwide]
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Discussion | The name Amaranthus torreyi has been widely misapplied to at least two other species, 7. A. arenicola and 6. A. watsonii. Because of that, the name A. bigelovii was used for A. torreyi by J. D. Sauer (1955) and in some recent floras. Sometimes A. torreyi (California and Arizona) and A. bigelovii (New Mexico and Texas) are recognized as separate species. The nomenclature and taxonomic relationships in this group should be critically reviewed based on type specimens and additional experimental and field studies. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Amaranthus spinosus is native to lowlands in tropical America; at present it is a pantropical weed that also occurs in some warm-temperate regions. Amaranthus spinosus, or its ancestral taxon, probably gave rise to the allopolyploid A. dubius by hybridization with some species of the A. hybridus aggregate (see above). Section Centrusa probably occupies a basal position, at least for the clade of subg. Amaranthus sect. Amaranthus, and probably for some representatives of subg. Acnida as currently outlined. Recent results of sequencing the ITS region (including ITS-1, 5.8S rDNA, and ITS-2) of nuclear ribosomal DNA from 15 species of Amaranthus occurring in China also suggest the basal position of A. spinosus among the studied species (Song B. H. et al. 2000). These results also confirm a profound divergence between subgenera Amaranthus and Albersia; the latter is called “sect. Paucestamen by the above authors. Data on the electrophoretic variation of seed proteins (R. H. Sammour et al. 1993) are also in accord with the segregation of these two subgenera; in the cited article, these groups are called sect. Amaranthus and sect. Blitopsis. (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 | Amblogyna torreyi, Amblogyna bigelovii, A. pringlei, Sarratia berlandieri var. emarginata | |
Name authority | (A. Gray) S. Watson: in W. H. Brewer et al., Bot. California 2: 42. (1880) | Linnaeus: Sp. Pl. 2: 991. (1753) |
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