Lythrum portula |
Lythraceae |
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broad leaf loosestrife, European loosestrife, European water-purslane, spatula-leaf loosestrife, water purslane |
loosestrife family |
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Habit | Herbs annual, slender, delicate, 0.5–2.5 dm, green, glabrous. | Herbs, annual or perennial, shrubs, subshrubs, or trees, terrestrial, amphibious, or aquatic, usually unarmed (armed in Punica), rarely glaucous, clonal or not. | ||||||||||||||||||||||||||||||||||||||||
Stems | frequently creeping and rooting at nodes, procumbent, decumbent, or weakly erect, often branched near base. |
erect, decumbent, lax, spreading, creeping, trailing, floating, or submerged, young ones often 4-angled. |
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Leaves | opposite; sessile; blade spatulate or oblong to broadly obovate or orbiculate, 5–15 × 3–8 mm, base narrowly attenuate. |
deciduous, usually opposite, sometimes alternate, subalternate, or whorled, simple, rarely dimorphic, emergent and submerged leaves dissimilar; stipules usually absent; sessile, subsessile, or petiolate; blade membranous [leathery], venation brochidodromous, each marginal vein forming a series of loops, margins entire (except coarsely toothed in Trapa), trichomelike glands present in axil at petiole base. |
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Inflorescences | spikelike. |
indeterminate or determinate, terminal or axillary, racemes, spikes, cymes, panicles, [thyrses], or flowers solitary; bracts absent (except present in Cuphea aspera); bracteoles present, paired on pedicels. |
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Flowers | opposite or alternate, along most of stem, sessile to subsessile, monostylous; floral tube broadly campanulate, 1 × 1.5 mm; epicalyx segments equal to or to 2 times longer than sepals; sepals 1/3–1/2 floral tube length, apex dark red; petals early caducous, 0 or 6, white to pink or rose, 1 × 0.7 mm; nectary absent; stamens 6. |
bisexual [unisexual], actinomorphic or zygomorphic; perianth and androecium usually perigynous (semi-epigynous to epigynous in Punica, perigynous to semi-epigynous in Trapa), mono-, di-, or tristylous; floral tube or cup persistent, campanulate, turbinate, urceolate, cylindrical, or obconic, green (except red or yellow in some Cuphea and Punica), sometimes conspicuously ribbed; sepals persistent, 4–8, valvate, usually deltate, sometimes subulate in Lythrum, alternating with segments of epicalyx or epicalyx absent; petals usually caducous or deciduous, rarely persistent, 0–8, distinct, on interior margin of floral tube between sepals, crinkled, pinnately-veined; nectary present as distinct organ, as nectariferous tissue in wall of ovary or floral tube, or absent; stamens (1–)4–42[+], usually equal to or 2 times number of petals, usually in 2 whorls of unequal length, sometimes 1 whorl; anthers versatile [or basifixed], introrse, 2-locular, longitudinally dehiscent; pistil 1; ovary usually superior (semi-inferior to inferior in Punica and Trapa), 2–6-locular (to 9 twisted locules in Punica); placentation axile, placenta elongate or globose; septa incomplete near ovary apex (reduced to thin threads in Cuphea); style 1; stigma 1, capitate to punctiform, dry (wet in Heimia, Lagerstroemia, and Punica); ovules 1–1400, anatropous, bitegmic. |
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Fruits | capsules, walls usually thin and dry (thick in Decodon, woody in Lagerstroemia), or leathery berries (Punica), or indurated, 2–4-horned drupes (Trapa), usually smooth (striate in Rotala), dehiscence loculicidal, septicidal, or septifragal, or indehiscent and splitting irregularly. |
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Capsules | surpassing floral tube, indehiscent, splitting irregularly. |
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Seeds | ca. 10–25, subglobose. |
3–250(–1400), usually brown (wine in Punica) [black, red], narrowly obovoid to fusiform, oblong to pyramidal, obovoid-semiovoid, semiorbicular, suborbicular, or elliptic (in outline), usually dry, fleshy in Punica, winged or not; endosperm not developed; embryo straight, oily, cotyledons usually ± complanate, rarely rolled, often auriculate or cordate. |
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2n | = 10 (Europe). |
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Lythrum portula |
Lythraceae |
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Phenology | Flowering summer–fall. | |||||||||||||||||||||||||||||||||||||||||
Habitat | Drying ponds, lake margins, shallow water. | |||||||||||||||||||||||||||||||||||||||||
Elevation | 1000–2200 m. (3300–7200 ft.) | |||||||||||||||||||||||||||||||||||||||||
Distribution |
CA; OR; WA; BC; Europe; n Africa [Introduced in North America]
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North America; nearly worldwide; mostly in tropical and subtropical areas |
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Discussion | Lythrum portula was long regarded as belonging to Peplis and is still accepted in that genus in some floras (D. A. Webb 1967). It is widespread in western Asia and Europe and has become established in the northwestern United States and adjacent Canada. It may be expected occasionally elsewhere in cool temperate regions in the flora area, as suggested by a 1999 introduction in Lake County, Ohio, presumably by seeds in soil accompanying plants purchased from a nursery on the West Coast. The Ohio population was recognized as non-native and destroyed (J. K. Bissell, pers. comm.). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Genera 28, species ca. 600 (10 genera, 32 species in the flora). Lythraceae are widely distributed in both hemispheres, generally in wet habitats, with limited temperate representation. Taxa of Lythraceae in the flora area range in elevation from coastal plain to mid montane. Elevational ranges of the species are approximations based on regional topography taken from collection data where possible. Lythraceae (order Myrtales) have recently been expanded to include the previously recognized families Duabangaceae, Punicaceae, Sonneratiaceae, and Trapaceae. Together they form a monophyletic family sister to Onagraceae (S. A. Graham et al. 2005). The traditional, more narrowly defined family (E. Koehne 1903) was divided into two tribes and four subtribes, a classification not supported by morphological or molecular phylogenetic evidence (Graham et al. 2011). Lythraceae are notably among only 28 angiosperm families that have evolved a heterostylous breeding system and one of three families in which the tristylous condition has evolved (S. C. H. Barrett et al. 2000). Six genera (Adenaria, Ammannia, Decodon, Lythrum, Pemphis, and Rotala) have distylous and/or tristylous species. Seed coats of many of the genera possess mucilaginous trichomes in the outermost cell layer that evaginate upon wetting, coming to resemble fungal growth. In Cuphea and in some genera outside the flora area, the trichomes reach half the length of the seeds and are spirally twisted. Floral merosity is highly variable in the family, and it is common to find a range of merosity in flowers of a single plant or within a population. The most frequent states are 4- and 6-merous. Only Decodon is commonly 5-merous. Submerged portions of the stems of the marsh-inhabiting genera Ammannia, Decodon, Lythrum, and Trapa can develop external spongy, aerenchymatous tissue that enhances oxygen exchange to the interior. Some genera are widely cultivated: Cuphea and Lagerstroemia as landscape and garden plants, Punica for the pomegranate fruit, and Lawsonia for the leaves from which henna dye is obtained. Trapa and some species of Lythrum and Rotala can be invasive and pose significant problems for wetlands and river systems in North America. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 10. | FNA vol. 10. | ||||||||||||||||||||||||||||||||||||||||
Parent taxa | Lythraceae > Lythrum | |||||||||||||||||||||||||||||||||||||||||
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Synonyms | Peplis portula | |||||||||||||||||||||||||||||||||||||||||
Name authority | (Linnaeus) D. A. Webb: Feddes Repert. 74: 13. (1967) | J. Saint-Hilaire | ||||||||||||||||||||||||||||||||||||||||
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