Hibiscus |
Hibiscus schizopetalus |
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hibiscus, rose-mallow |
Chinese lantern, fringe rose-mallow or hibiscus, fringe rosemallow |
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Habit | Herbs, annual or perennial, subshrubs, shrubs, or trees, glabrous or hairy. | Shrubs or trees, to 3(–5) m. Stems: new growth essentially glabrous, lines of curved hairs absent. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stems | erect, Inflorescences axillary, sometimes adnate to subtending petiole (H. moscheutos), flowers solitary or clustered; involucel present, bractlets usually persistent, rarely deciduous (H. mutabilis), 6–16, rarely minute or absent (H. denudatus), distinct, undivided, 2-fid or appendaged (H. acetosella, H. aculeatus, H. furcellatus, H. radiatus). |
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Leaves | stipules narrowly triangular, 1–2.5 mm; petiole to 1/3 blade, adaxial groove hairy with minute, ± sinuous hairs; blade lanceolate-ovate to ovate, unlobed, 3.5–10.5 × 1.5–4 cm, base rounded to cuneate, margins coarsely serrate in distal 2/3–3/4, apex acute to short-acuminate, ± pinnately veined, surfaces glabrate, nectary present abaxially on midvein near base. |
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Inflorescences | solitary flowers in axils of distal leaves. |
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Pedicels | jointed at middle or distally, 7.5–15 cm; involucellar bractlets 6–8, triangular, 0.06–0.18 cm, margins not ciliate. |
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Flowers | usually lasting for a day; calyx persistent, sometimes accrescent, inflated or not, not spathaceous, primary veins usually ± straight, rarely zigzag (H. trionum, sometimes H. dasycalyx), lobes triangular to trullate, sometimes strongly 3-ribbed (H. acetosella, H. aculeatus, H. furcellatus, H. radiatus), sometimes with nectary on midrib; corolla radial or weakly bilaterally symmetric, narrowly funnelform to broadly campanulate or rotate or petals sometimes recurved (H. clypeatus), white, cream, yellow, orange, pink, red, lavender, purple, or blue, usually red, purple, or brown basally; staminal column included or exserted (H. coccineus, H. poeppigii, H. schizopetalus); ovary 5-carpellate; ovules 8–60 per carpel; styles 5-branched from or beyond orifice of staminal column; stigmas capitate to discoid or wedge-shaped (H. striatus). |
pendulous; calyx divided 1/8–1/2 length, often 3-lobed, tubular to narrowly funnelform, (1–)1.4–2 cm, lobes broadly triangular, apices acute to obtuse, glabrate, neither accrescent nor inflated, nectaries absent; petals strongly recurved, rose-pink to red, darker on veins, broadly to narrowly obovate, deeply and irregularly pinnatifid-laciniate, 4–6.5 × 1.5–3.5 cm, glabrous; staminal column straight or curved apically, pendulous, pink to red, 5.5–9 cm, bearing filaments in distal 1/3–1/2, free portion of filaments not secund, 4.5–7.5 mm; pollen yellow; styles pink to red, 7–15 mm; stigmas pink to red. |
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Fruits | capsules, 5-valved, ovoid or spheroid, apex usually apiculate, acute, or acuminate, sometimes rounded or depressed or impressed, glabrous or hairy. |
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Capsules | brown, oblong-cylindric, 3.5–4 cm, glabrous or puberulent. |
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Seeds | to 60 per locule, reniform-ovoid, reniform-globose, or subglobose, sometimes angulate, sometimes laterally compressed or impressed, papillose or not, glabrous or hairy. |
brown, angulately reniform-ovoid, 2–3 mm, smooth, glabrous or puberulent. |
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x | = 10, 11, [12,] 14, [15–17,] 18, 19, [20,] 26, [27,] and probably higher. |
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2n | = 34, 40, 42, 45 (all cultivars). |
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Hibiscus |
Hibiscus schizopetalus |
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Phenology | Flowering year-round. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Habitat | Disturbed sites | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Elevation | 0–50 m (0–200 ft) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Distribution |
North America; Mexico; Central America; South America; West Indies; Eurasia; Africa; Indian Ocean Islands; Pacific Ocean Islands; Australia |
FL; e Africa [Introduced in North America; introduced also in Mexico, West Indies, Central America, South America, s Asia, elsewhere in Africa, Pacific Islands, Australia] |
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Discussion | Species ca. 350 (21 in the flora). Taxonomy of Hibiscus is in flux. Molecular studies place members of some other genera in Hibiscus as traditionally circumscribed, indicating paraphyly (B. E. Pfeil and M. D. Crisp 2005). Neither of the two solutions to this problem—vastly expanding the circumscription of Hibiscus to include the nested genera, or breaking Hibiscus into smaller genera—has been attempted here. The 21 species of Hibiscus in the flora area are scattered among nine sections. The sections follows: sect. Hibiscus (species 1), sect. Bombicella de Candolle (species 2–6), sect. Furcaria de Candolle (species 7–10), sect. Lilibiscus Hochreutiner (species 11 and 12), sect. Muenchhusia (Heister ex Fabricius) O. J. Blanchard (species 13–17), sect. Venusti Ulbrich (species 18), sect. Striati O. J. Blanchard (species 19), sect. Trionum de Candolle (species 20), and sect. Clypeati O. J. Blanchard (species 21). Most Hibiscus species in the flora area are native; seven were introduced into North America either for horticultural purposes (H. acetosella, H. mutabilis, H. rosa-sinensis, H. schizopetalus, H. syriacus, and H. trionum) or as fiber crops (H. radiatus). Experimental crosses among some native species (H. coccineus, H. grandiflorus, H. laevis, and H. moscheutos) have been the basis of selections of hardy Hibiscus available in the horticultural trade. A popular cultivated form in the South is the result of an experimental cross involving a complex interspecific hybrid combining H. coccineus, H. laevis, and H. moscheutos as the staminate parent and H. mutabilis as the pistillate parent (H. F. Winters 1970). North American taxa in the speciose sect. Bombicella share a base chromosome number of × = 11 (chromosome numbers are unknown for Hibiscus coulteri); those in sect. Furcaria, × = 18; and those in sect. Muenchhusia, × = 19. Base numbers of the two sections represented in the flora area by one native species each are 10 and 26, and cannot be readily reconciled between themselves or with the others. The remaining four sections together include five species, all of which are non-natives and, except for H. trionum, have long histories in cultivation and multiple different chromosome numbers that are not easily evaluated. This overall chromosomal diversity supports the molecular evidence for a polyphyletic Hibiscus. Extensive experimental hybridization work in sect. Furcaria, and the study of chromosome pairing relationships in these hybrids, indicate that the native species Hibiscus aculeatus and H. furcellatus, both tetraploids, share the genomic makeup GGPP, while the introduced species H. acetosella and H. radiatus, also tetraploids, share AABB (F. D. Wilson 1994). A naturally occurring hybrid between Hibiscus coulteri and H. denudatus (Hibiscus ×sabei Weckesser) has been documented from western Texas (W. Weckesser 2011). Some desert species of Hibiscus sometimes produce cleistogamous flowers. Foliar nectaries are present abaxially near the base of the midvein in some species. Three species of Hibiscus are of doubtful status in the flora area. Hibiscus cannabinus Linnaeus and H. sabdariffa Linnaeus have both been cultivated in the southern states as fiber crops, and the latter also for its fleshy calyces, which are used to flavor beverages. It is doubtful that either has become established in the flora area. Hibiscus bifurcatus Cavanilles is widely distributed from the West Indies and Guatemala to South America; it was documented with two collections from Dade County in Florida by R. Woodbury in 1949 and 1950, but since Woodbury was involved at the time in establishing what later became the John C. Gifford Arboretum in Coral Gables south of Miami, there is a good chance that the source was a plant in cultivation. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Apparently native only in Kenya, Tanzania, and perhaps Mozambique, Hibiscus schizopetalus is widely cultivated in the Tropics and occasionally escapes. The occurrence in many H. rosa-sinensis cultivars of semipendulous, long-pedicelled flowers with variously crenate, undulate petals suggests the involvement of H. schizopetalus. Hybrids between H. schizopetalus and H. rosa-sinensis can be called H. ×archeri W. Watson. Typification of H. schizopetalus was discussed by M. Cheek (1989). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 6, p. 252. | FNA vol. 6, p. 261. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Synonyms | H. rosa-sinensis var. schizopetalus | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | Linnaeus: Sp. Pl. 2: 693. (1753): Gen. Pl. ed. 5, 310. (1754) | (Dyer) Hooker f.: Bot. Mag. 106: plate 6524. (1880) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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