Ludwigia peruviana |
Ludwigia polycarpa |
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Peruvian primrose-willow |
false loosestrife, many-fruit water-primrose, manyfruit primrose-willow |
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Habit | Herbs often woody at base, with peeling bark. | Herbs slender, with well-developed aerenchyma on submerged stems, forming stolons 2.5–15(–22) cm, 1–2.3 mm thick, well branched. |
Stems | usually ridged, rarely succulent, profusely branched, 100–400 cm, usually villous, rarely glabrous, hairs deciduous in age, multicellular, usually tawny. |
erect or ascending, slightly ridged, well branched, (10–)25–60(–85) cm, glabrate with raised ± strigillose lines decurrent from leaf axils. |
Leaves | stipules deciduous, narrowly deltate, 1–1.5 × 0.3–0.5 mm, setaceous; petiole 0–1.5 cm; blade usually lanceolate, elliptic or broadly elliptic, sometimes ovate, obovate, or rounded, 2–45 × 1–10 cm, base obtuse or cuneate, rarely asymmetrical, margins entire or gland-toothed, apex usually acute or acuminate, rarely rounded and emarginate, mostly scabrid, membranous or papery, surfaces usually villous, sometimes glabrous; bracts usually not strongly reduced. |
alternate; stipules narrowly to broadly ovate, 0.1–0.4 × 0.1–0.3 mm; stolons: leaves often clustered near apex of stolon, petiole 0–0.5 cm, blade narrowly elliptic or oblanceolate, 0.8–2(–3.2) × 0.2–0.8(–1.2) cm, base attenuate, margins entire or remotely denticulate, apex acute, surfaces glabrous; stems: petiole winged, 0.1–1 cm, blade very narrowly oblong-elliptic, 3.5–11 × 0.4–1(–1.7) cm, base very narrowly cuneate or long-attenuate, margins entire and densely, minutely papillose-serrulate with obscure hydathodal glands, apex narrowly acute or acuminate, surfaces glabrous; bracts not much reduced. |
Inflorescences | leafy racemes, flowers solitary in distal axils; bracteoles deciduous, usually attached near base or on lower 1/2 of ovary, sometimes on upper pedicel, subtended by reduced, glandlike stipels, ovate or lanceolate to linear, 5–20 × 1–6 mm, apex acute or short-acuminate, surfaces villous. |
elongated, leafy spikes, flowers solitary in leaf axils, sometimes borne almost to base of stems; bracteoles attached 0.5–2.5(–3) mm distal to base of ovary, linear-lanceolate, 3.5–6.5(–8) × 0. |
Flowers | sepals ovate or ovate-lanceolate, 10–23 × 4–9 mm, apex acute or short-acuminate, sometimes glandular-serrulate; petals bright yellow, orbiculate or obovate, 10–40 × 10–40 mm, apex rarely emarginate, short-clawed; stamens 8(or 10) in 2 unequal series, yellow, shorter filaments 1.5–4 mm, longer ones 3.5–5 mm, anthers oblong, 3–6 mm; ovary obconic, 4- or 5-angled, sometimes subterete, 5–20 × 3–7 mm, narrowed to pedicel, usually densely villous, sometimes glabrous; nectary disc elevated 0.3–3.2 mm on ovary apex, 4–6 mm diam., 4(or 5)-lobed, sunken, ringed by long, white hairs; style 1.5–3.5 mm, stigma globose, 1.6–3.5 × 1.8–3.5 mm, usually as long as stamens, rarely exserted beyond them. |
sepals spreading horizontally with reflexed tips, pale green, narrowly ovate-deltate, 2.5–4.5 × 1.5–3.2 mm, margins entire, minutely papillose-serrulate, apex elongate-acuminate, surfaces glabrous; petals 0; filaments yellowish green, 0.7–1.5 mm, base dilated, anthers 0.5–0.9 × 0.5–0.7 mm; pollen shed in tetrads; ovary oblong, barely 4-angled, 3–4.5 × 2–3.5 mm; nectary disc elevated 0.5–0.8 mm on ovary apex, yellowish green, 1.8–3 mm diam., 4-lobed, glabrous; style yellowish green, 0.5–0.8 mm, glabrous, stigma broadly clavate to subglobose, 0.4–0.8 × 0.3–0.6 mm, usually 4-lobed, not exserted beyond anthers. |
Capsules | ± sharply 4- or 5-angled, 10–40 × 6–13 mm, thin-walled, irregularly dehiscent, pedicel 5–65 mm. |
oblong-obovoid, obscurely 4-angled, 4–7 × 2.5–5 mm, hard-walled, irregularly dehiscent, pedicel 0.1–0.3 mm. |
Seeds | brown or reddish brown, oblong, 0.6–0.9 × 0.3–0.4 mm, rounded at ends, with inconspicuous raphe. |
light brown, narrowly oblong with curved ends, 0.5–0.6 × 0.2–0.3 mm, surface cells elongate parallel to seed length. |
4 | –1(–1.3) mm, with a swollen base, margins minutely papillose-serrulate. |
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2n | = 64, 80, 96, 128. |
= 32. |
Ludwigia peruviana |
Ludwigia polycarpa |
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Phenology | Flowering Jun–Aug(–Sep) (sometimes in any month). | Flowering Jun–Sep. |
Habitat | Wet places, ditches, drainage canals, sloughs, swales, marshy shores, wet clearings. | Ditches, moist prairies, alluvial ground of ponds, lakes, and rivers, marshes, swales, edges of lagoons, low fallow fields. |
Elevation | 0–200[–2600] m. [0–700[–8500] ft.] | 100–300 m. [300–1000 ft.] |
Distribution |
AL; FL; GA; NC; TX; Central America; South America; Mexico (Chiapas, Durango, Oaxaca, Puebla, Tabasco, Veracruz); West Indies [Introduced in Eurasia (India, Indonesia, Singapore, Sri Lanka), Australia]
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CT; IA; ID; IL; IN; KS; KY; MA; MI; MN; MO; NE; OH; PA; VA; WI; WV; ON
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Discussion | Ludwigia peruviana is sometimes cultivated and naturalized, which may account for occurrences in North America and Eurasia. Except in the Amazon basin, where it is known only from few collections in western Amazonia, and in northeastern Brazil, where it is scarce, L. peruviana is common throughout its range, and may behave as a weed, especially along slow-flowing canals and drainage ditches. Ludwigia peruviana is also naturalized at scattered localities in Asia (P. H. Raven 1963[1964]) and around Sydney, Australia. The earliest collection from Asia is labeled “ex horto bot. Bogoriensi Javae misit 1869” (Raven). It also occurs locally in the Nilgiri Mountains of southwest India and in Sri Lanka, as well as in scattered locations in Bangka, Java, Malaysia, and Sumatra from sea level to 1000 m (Raven 1963[1964], 1978). Jussiaea grandiflora Ruíz & Pavon, a synonym for J. peruviana Linnaeus, appeared in 1830, not in 1802 (P. A. Munz 1942; P. H. Raven 1963[1964]); it is a later homonym of J. grandiflora Michaux (1803), as reported in W. Greuter and T. Raus (1987). Jussiaea hirta (Linnaeus) Swartz is an illegitimate homonym and J. hirta (Linnaeus) Vahl is an illegitimate isonym; both pertain here. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Ludwigia polycarpa, unlike all other species in sect. Isnardia, is distributed primarily in the central Midwest and Great Lakes regions, with one highly disjunct population recorded from Kootenai County, Idaho, which is presumably introduced. This species has also been found scattered as far east as Connecticut and Massachusetts, and reports of it from Arkansas, Maine, Tennessee, and Vermont cannot be confirmed. As indicated by C. I. Peng (1989), a report of this species from Alabama involved a natural hybrid between L. glandulosa and L. pilosa. The basal stolons formed by Ludwigia polycarpa tend to be shorter, more condensed, and more branched than those found in other species, and may be a morphological adaptation to perennial survival in the colder areas in which it grows. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 10. | FNA vol. 10. |
Parent taxa | ||
Sibling taxa | ||
Synonyms | Jussiaea peruviana, J. hirsuta, J. macrocarpa, J. mollis, J. peruviana var. glaberrima, J. speciosa, J. sprengeri, L. hirta, Oenothera hirta | Isnardia polycarpa |
Name authority | (Linnaeus) H. Hara: J. Jap. Bot. 28: 293. (1953) | Short & R. Peter: Transylvania J. Med. Assoc. Sci. 8: 581. (1835) |
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