Heteranthera reniformis |
Heteranthera multiflora |
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kidney-leaf mud-plantain |
bouquet mudplantain |
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Habit | Plants annual or facultatively perennial. | Plants annual. |
Vegetative stems | submersed with elongate internodes, or emersed and procumbent. |
submersed with elongate internodes, or emersed and procumbent. |
Flowering stems | 1–9 cm, distal internode 0.5–4 cm. |
1–4 cm, distal internode less than 1 cm. |
Inflorescences | spicate, 2–8-flowered, elongating in 1 day, usually shorter than spathes, terminal flower sometimes extending beyond spathe apex; spathes 0.8–5.5 cm, glabrous; peduncle 0.5–4.2 cm, glabrous. |
spicate, 3–16-flowered, elongating in 1–2 days, longer than spathes (except on cleistogamous inflorescences); spathes 2–7 cm, glabrous; peduncle 4–11 cm, glabrous when emersed. |
Flowers | opening ca. 3 hours after sunrise, wilting by early afternoon; perianth white, salverform, tube 5–10 mm, limbs zygomorphic, lobes narrowly elliptic, 3–6.5 mm, distal central lobe with yellow or green region at base, sometimes with distal brown spot; stamens unequal, lateral stamens 0.9–2.2 mm, filaments linear, pubescent with white multicellular hairs toward apex; central stamen 2.2–4.7 mm, filament sparsely pubescent with multicellular hairs; style pubescent with multicellular hairs. |
opening ca. 2 hours after dawn, wilting early afternoon; perianth mauve or white, salverform, tube 3–12 mm, limbs zygomorphic, lobes narrowly elliptic, 3.3–5.9 mm, distal central lobe dark purple in basal 1/3, 2 yellow spots within dark area; stamens unequal, lateral stamens 1.3–2.4 mm, filaments linear, densely pubescent with purple multicellular hairs toward apex; central stamen 2.6–4 mm, filament sparsely pubescent with multicellular hairs; style pubescent with multicellular hairs. |
Seeds | 8–14-winged, 0.5–0.9 × 0.3–0.5 mm. |
9–12-winged, 0.6–0.9 × 0.4–0.5 mm. |
Sessile | leaves forming basal rosette, blade linear to oblanceolate, thin, 2.4–3.7 cm × 3–8 mm. |
leaves alternate; blade linear to oblanceolate, thin, 37–70 × 4–6 mm, margins entire. |
Petiolate | leaves floating or emersed; stipule 1–5 cm; petiole 2–13 cm; blade reniform, 1–4 × 1–5 cm, length equal to or less than width, apex obtuse. |
leaves floating or emersed; stipule 3–5 cm; petiole 5–15 cm; blade cordate, 2–5 × 2–5 cm, length usually greater than width, apex obtuse. |
2n | = 48. |
= 32. |
Heteranthera reniformis |
Heteranthera multiflora |
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Phenology | Flowering Jun–Oct. | Flowering Jul–Nov. |
Habitat | Roadside ditches, edges of streams and ponds, freshwater tidal mudflats | Roadside ditches, pond edges |
Elevation | 0–2600 m (0–8500 ft) | 0–1800 m (0–5900 ft) |
Distribution |
AL; CT; DE; FL; GA; IL; IN; KY; LA; MD; MO; MS; NC; NJ; NY; OH; PA; SC; TN; TX; VA; WV; Mexico; throughout Central America; scattered in South America (Argentina, Brazil, Paraguay); naturalized in Italy
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AR; DE; IA; IL; KS; LA; MD; MO; MS; NC; NE; NJ; OK; PA; TN; TX; VA; South America (Argentina, Brazil, Paraguay, Venezuela)
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Discussion | This species has in the past been incorrectly identified as either Heteranthera reniformis (J. A. Steyermark 1963) or H. peduncularis (R. B. Kaul and C. N. Horn 1986). However, detailed study of development, floral morphology, and chromosome number revealed distinct differences (C. N. Horn 1985, 1988). Three distinct genetic forms of this species exist, two in the flora range. Populations along the Atlantic coast have white flowers and inflorescences with most of the flowers within the spathe. Populations in the Great Plains have blue flowers and inflorescences with most flowers typically beyond the spathe. These populations have not been, nor should they be, recognized at any taxonomic level. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Source | FNA vol. 26, p. 43. | FNA vol. 26. |
Parent taxa | Pontederiaceae > Heteranthera | Pontederiaceae > Heteranthera |
Sibling taxa | ||
Synonyms | Heterandra reniformis | H. reniformis var. multiflora |
Name authority | Ruiz & Pavon: Fl. Peruv. 1: 43. (1798) | (Grisebach) C. N. Horn: Phytologia 59: 290. (1986) |
Web links |