Genus Stephania in Family Menispermaceae
In botanical taxonomy, a genus (plural genera) is a rank used to group closely related species within a family. In the hierarchy, genus sits below family and above species.
Genera are defined by shared morphological, anatomical, and genetic characteristics (for example, features of flowers, fruits, seeds, or leaves) that indicate a close evolutionary relationship among the species they contain.
Each genus can include one or more species. Examples include Rosa (roses) and Solanum (nightshades, including tomato and eggplant).
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Genus Description
Suggest a correction!Stephania Lour., a genus of twining lianas and herbaceous climbers in the family Menispermaceae, comprises roughly 50 species (POWO, 2024; WFO, 2024). It occurs from sea level to about 2000 m in tropical Asia, with secondary centres in Africa and Madagascar. No formal type species is designated, though Stephania japonica often serves as the nomenclatural anchor (APG IV, 2016).
Stephania bears alternate, simple, often peltate leaves with caducous stipules. Plants are dioecious, bearing tiny unisexual flowers in axillary cymes. The perianth has five sepals and reduced petals; the androecium bears six to many free stamens, and the ovary has 6–12 free carpels each with a single ovule. Fruit is a laterally compressed drupe with a hard endocarp.
Species richness peaks in Southeast Asia (Malay Peninsula, Borneo, Philippines); a secondary centre occurs in tropical Africa, the Congo Basin and West Africa. Stephania inhabits lowland rainforests, montane cloud forests, limestone cliffs and mangroves as twining lianas. Elevations range from sea level to about 2000 m; S. dielsiana reaches Himalayan slopes, S. rotunda is confined to coastal mangroves.
Flowers are pollinated by flies and beetles attracted to fragrant inflorescences, a pattern typical of Menispermaceae (Renner & Kato, 2019). Drupes are eaten by birds, dispersing seeds. Cytological data suggest a base chromosome number of x = 13 (Huang & Keng, 1974). Plants are perennial lianas that flower at start of rainy season, fruiting before leaf drop.
Early sectional concepts of Stephania (e.g., sects. Stephania and Myrtosepalum) are superseded by molecular phylogenies. Plastid and nuclear data place the genus as monophyletic, split into Asian and African lineages (Wang et al., 2019; Kool & Thulin, 2017). Recent re‑circumscriptions synonymise Asian taxa with African ones, indicating morphological divergence. Stephania sensu lato is retained, treating Cocculus and Arcangelisia as distinct, a view backed by genome‑scale analyses (Kool & Thulin, 2017).
Stephania species such as S. erecta and S. japonica are cultivated as ornamental climbers for attractive foliage (Plants of the World Online, 2024). No species are used for timber, and most have only horticultural value or occur as occasional weeds in disturbed sites.
Many taxa remain data deficient in global assessments, reflecting limited field surveys and taxonomic uncertainty (IUCN Red List, 2023). Habitat loss from deforestation and forest fragmentation, combined with collection for horticulture, poses ongoing threats. Continued targeted fieldwork and integrative taxonomy will be essential to clarify species limits and guide conservation planning.
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Stephania abyssinica (Walp.)
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Stephania andamanica (Diels)
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Stephania bancroftii (F.M.Bailey)
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Stephania brachyandra (Diels)
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Stephania brevipedunculata (C.Y.Wu & D.D.Tao)
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Stephania brevipes (Craib)
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Stephania cambodica (Gagnep.)
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Stephania capitata ((Blume) Spreng.)
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Stephania cephalantha (Hayata)
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Stephania chingtungensis (H.S.Lo)
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Stephania corymbosa (Walp.)
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Stephania crebra (Forman)
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Stephania cyanantha (Welw. ex Hiern)
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Stephania delavayi (Diels)
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Stephania dentifolia (H.S.Lo & M.Yang)
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Stephania dicentrinifera (H.S.Lo & M.Yang)
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Stephania dictyoneura (Diels)
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Stephania dielsiana (Wu)
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Stephania dinklagei (Diels)
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Stephania dolichopoda (Diels)
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Stephania ebracteata (S.Y.Zhao & H.S.Lo)
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Stephania elegans (Hook.f. & Thomson)
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Stephania epigaea (H.S.Lo)
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Stephania excentrica (H.S.Lo)
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Stephania formanii (Kundu & S.Guha)
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Stephania glandulifera (Miers)
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Stephania gracilenta (Miers)
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Stephania grandiflora (Forman)
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Stephania hainanensis (H.S.Lo & Y.Tsoong)
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Stephania herbacea (Gagnep.)
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Stephania intermedia (H.S.Lo)
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Stephania japonica ((Thunb.) Miers)
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Stephania kaweesakii (Jenjitt. & Ruchis.)
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Stephania kuinanensis (H.S.Lo & M.Yang)
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Stephania kwangsiensis (H.S.Lo)
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Stephania lincangensis (H.S.Lo & M.Yang)
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Stephania longa (Lour.)
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Stephania longipes (H.S.Lo)
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Stephania macrantha (H.S.Lo & M.Yang)
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Stephania mashanica (H.S.Lo & B.N.Chang)
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Stephania merrillii (Diels)
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Stephania micrantha (H.S.Lo & M.Yang)
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Stephania mildbraedii (Diels)
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Stephania miyiensis (S.Y.Zhao & H.S.Lo)
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Stephania moluccana (Forman)
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Stephania montana (Diels)
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Stephania neoguineensis (Kundu & S.Guha)
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Stephania novenanthera (Heng C.Wang)
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Stephania oblata (Craib)
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Stephania officinarum (H.S.Lo & M.Yang)
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Stephania papillosa (Craib)
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Stephania pierrei (Diels)
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Stephania polygona (N.H.Xia & V.T.Chinh)
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Stephania psilophylla ((C.Presl) Forman)
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Stephania renifolia (Forman)
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Stephania reticulata (Forman)
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Stephania rotunda (Lour.)
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Stephania salomonum (Diels)
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Stephania sinica (Diels)
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Stephania suberosa (Forman)
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Stephania subpeltata (H.S.Lo)
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Stephania succifera (H.S.Lo & Y.Tsoong)
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Stephania sutchuenensis (H.S.Lo)
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Stephania tetrandra (S.Moore)
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Stephania tomentella (Forman)
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Stephania tuberosa (Forman)
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Stephania venosa ((Blume) Spreng.)
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Stephania viridiflavens (H.S.Lo & M.Yang)
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Stephania wightii ((Arn. ex Wight) Dunn)
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Stephania yunnanensis (H.S.Lo)
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Stephania zippeliana (Miq.)