Flora of North America species comparison

Species 19 (18 in the flora).

Based on recent molecular and genomic analyses of the monophyletic group of North Temperate haplostemonous species (Liu S. H. et al. 2017), sect. Isnardia (previously referred to as sect. Dantia Baillon; C. I. Peng et al. 2005) has been expanded to include the species treated previously as sect. Microcarpium (Peng 1988, 1989). Section Isnardia now comprises a polyploid complex of 19 species with a center of distribution in the southeastern United States. Most species are restricted to the Gulf and/or southeastern Coastal Plains, usually from Florida to Texas and to New Jersey. Several species extend farther north (L. glandulosa and L. sphaerocarpa) or only occur farther north (L. polycarpa); L. palustris occurs widely across eastern North America from Newfoundland, Quebec, Minnesota, and Kansas to the Gulf and east coasts, is well established on the west coast from California to British Columbia, ranges south to the West Indies, Mexico, Central America, and northern South America, and also occurs in Europe. Ludwigia repens also extends to the West Indies and Mexico, with disjunct occurrences in Arizona, California, and Oregon; several other species also extend to the West Indies, and L. stricta (C. Wright ex Grisebach) C. Wright is endemic to Cuba (Peng and H. Tobe 1987; Peng 1988, 1989).

Section Isnardia now consists of five diploids (2n = 16), nine tetraploids (2n = 32), four hexaploids (2n = 48), and one octoploid (2n = 64); one diploid, Ludwigia stricta, does not occur in North America. Species in this treatment are arranged by ploidy level, then by presumed genomic and phylogenetic order (H. Tobe et al. 1988; C. I. Peng 1988, 1989). Despite the different ploidy levels, natural hybridization among the species of this section is relatively common, and all species above the diploid level are allopolyploid (Peng 1988, 1989; Peng et al. 2005). Most hybrids are sterile, but may persist vegetatively. One sterile hybrid, L. ×lacustris Eames (L. brevipes × L. palustris), has persisted in the same area in Connecticut and Rhode Island for at least 70 years through vegetative reproduction; one of its parents, L. brevipes, no longer occurs in this region (Peng et al. 2005).

Most species in sect. Isnardia have stolons and fibrous roots, and the more aquatic species have aerenchyma near the base of their stems. Five species (the former sect. Dantia, in the strict sense) differ from all others in Ludwigia by having opposite rather than alternate leaves. Most species (14 of 19 in the section) have no petals (some occasionally have one to four vestigial petals). Eight species shed their pollen as monads, most others as tetrads. Some of the apetalous species have showy sepals that are creamy white, light yellow, or light green, and insect visitors have been observed visiting them (C. I. Peng 1989; Peng et al. 2005); all species in the section that have been tested are self-compatible, and only Ludwigia arcuata has large enough flowers, with the stigma regularly exserted beyond the anthers, that it regularly outcrosses.

Several species in sect. Isnardia are popular aquarium plants due to their aquatic nature and small stature.

Several superfluous generic names have been proposed for this section, including Dantia Boehmer (and several combinations based on the genus at the sectional level).

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Genera 22, species 664 (17 genera, 277 species in the flora).

Members of the Onagraceae are especially richly represented in North America. The family comprises annual and perennial herbs, with some shrubs and a few small to medium-sized trees. Most species occur in open habitats, ranging from dry to wet, with a few species of Ludwigia aquatic, from the tropics to the deserts of western North America, temperate forests, and arctic tundra; some species of Epilobium, Ludwigia, and Oenothera can be weeds in disturbed habitats. Members of the family are characterized by 4-merous flowers (sometimes 2-, 5-, or 7-merous), an inferior ovary, a floral tube in most species, stamens usually two times as many as sepals, and pollen connected by viscin threads. Flowers are usually bisexual, sometimes unisexual, and plants are gynodioecious, matinal, diurnal, or vespertine, self-compatible or self-incompatible, often outcrossing and then pollinated by a wide variety of insects or birds, or autogamous (P. H. Raven 1979; W. L. Wagner et al. 2007).

Onagraceae are known in considerable systematic detail, and information is available on comparative breeding systems and pollination biology, on chromosome numbers and cytogenetic relations, often involving translocations, and on vegetative, floral, and seed anatomy, palynology, and embryology. The phylogeny of the family is known in reasonably good detail, with most parts of the trees generally well-supported.

The suprageneric and generic classification presented by W. L. Wagner et al. (2007) differs in a number of ways from the previous classification (P. H. Raven 1979, 1988). Onagraceae are divided into two subfamilies based on a fundamental basal split recognized in all phylogenetic studies (R. H. Eyde 1981; P. C. Hoch et al. 1993; R. A. Levin et al. 2003, 2004; V. S. Ford and L. D. Gottlieb 2007), with Ludwigia on one branch (as Ludwigioideae), and the rest of the family on a second branch (as Onagroideae). Onagroideae are subdivided into six tribes: Circaeeae (including Fuchsieae), Epilobieae, Gongylocarpeae, Hauyeae, Lopezieae, and Onagreae. The Epilobieae and Onagreae are diverse; together they constitute fully two-thirds of the species in the family and include 15 of the 22 genera. The classification following Wagner et al. can be viewed on the Onagraceae web site by Wagner and Hoch at http://botany.si.edu/Onagraceae.

(Discussion copyrighted by Flora of North America; reprinted with permission.)