Genus Erycibe in Family Convolvulaceae
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!Erycibe (Roxb.) is a climbing, lianescent genus in Convolvulaceae placed in tribe Merremieae by recent revisions (Staples, 2006). About 90 species are accepted (POWO, 2024; Staples, 2006), distributed from India and Sri Lanka through mainland Southeast Asia, Malaysia, Indonesia, the Philippines, Papua New Guinea to northeastern Australia and the western Pacific (Staples, 2006; WFO, 2024). The type species is Erycibe tomentosa Benth., long recognized in the group (Staples, 2006).
Diagnostic traits are well summarized in regional treatments: woody twiners with opposite leaves and minute stipules; indumentum typically of simple hairs (sometimes absent). The calyx is apically reflexed with a distinct central apiculus, the corolla is white to cream, funnel-shaped, five-lobed with five marked midpetaline bands and a finely pilose limb; a whorl of five stamens is inserted near the base of the corolla tube, and the style is entire to slightly bilobed. Fruits are drupes with a thin exocarp and a hard endocarp, and the ovary is bilocular with two pendulous ovules per locule (Staples, 2006).
Centers of diversity lie in the Indo-Burma hotspot and in the Malesian region, with numerous endemics in the Malay Peninsula, Borneo, Sumatra, and New Guinea. Most species are lianas of lowland to lower montane tropical forests and secondary vegetation, though some extend into submontane zones and one Australian species reaches sclerophyll forest margins (Staples, 2006). A clear biogeographic pattern connects Indo-Malesian and Australasian taxa via repeated dispersal across Wallacea, consistent with molecular work positioning Erycibe within a Merremieae clade that includes Australasian and Asian lineages (Stefanović et al., 2002).
Pollination and seed dispersal biology remain minimally documented. Chromosome numbers reported across the Convolvulaceae show x=15 as prevalent, but a stable base number for Erycibe is not yet firmly established (Staples, 2006). Anatomically, the lianescent habit is reflected in expanded secondary xylem and pericycle fiber development characteristic of climbing Convolvulaceae.
No sectional or subgeneric classification has gained broad acceptance; Erycibe is treated as a coherent but internally variable genus in recent monographic and regional floras, with synonymy concentrated in historical names rather than formal rank-based groupings (Staples, 2006). Alternative placements have been explored in phylogenetic studies but do not alter the tribe-level alignment (Stefanović et al., 2002). Some floras retain Neuropeltis as distinct, while others merge it into Erycibe, highlighting unresolved boundaries and the need for further phylogenetic testing (Staples, 2006).
Species are widely used in horticulture as ornamental climbers in tropical gardens; the genus is not a major crop or timber group, and invasive tendencies are not widely reported (Staples, 2006).
Threats derive primarily from deforestation across Indo-Malesian centers, compounded by incomplete taxonomic resolution and sparse conservation assessments in many range countries (POWO, 2024). Continued field work and phylogenomic analyses are required to resolve Erycibe’s internal structure and protect its diversity effectively (Stefanović et al., 2002).
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Erycibe aenea (Prain)
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Erycibe albida (Prain)
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Erycibe beccariana (Hoogland)
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Erycibe borneensis ((Merr.) Hoogland)
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Erycibe brassii (Hoogland)
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Erycibe brunneopilosa (Kochaiph. & Utteridge)
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Erycibe bullata (Ridl. ex Hoogland)
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Erycibe carrii (Hoogland)
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Erycibe citriniflora (Griff.)
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Erycibe clemensae (Ooststr.)
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Erycibe coccinea ((F.M.Bailey) Hoogland)
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Erycibe cochinchinensis (Gagnep.)
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Erycibe coriacea (Wall.)
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Erycibe crassipes (Ridl. ex Hoogland)
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Erycibe crassiuscula (Gagnep.)
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Erycibe elliptilimba (Merr. & Chun)
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Erycibe expansa (Wall. ex G.Don)
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Erycibe festiva (Prain)
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Erycibe floribunda (Pilg.)
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Erycibe forbesii (Prain)
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Erycibe glaucescens (Wall. & Choisy)
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Erycibe glomerata (Blume)
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Erycibe grandiflora (Adelb.apud Hoogl.)
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Erycibe grandifolia (Merr. ex Hoogland)
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Erycibe griffithii (C.B.Clarke)
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Erycibe hainanensis (Merr.)
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Erycibe hellwigii (Prain)
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Erycibe henryi (Prain)
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Erycibe hollrungii (Hoogland)
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Erycibe impressa (Hoogland)
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Erycibe induta (Pilg.)
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Erycibe kinabaluensis (Hoogland)
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Erycibe laurifolia (D.G.Long)
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Erycibe leucoxyloides (King ex Prain)
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Erycibe macrophylla (Hallier f.)
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Erycibe magnifica (Prain)
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Erycibe maingayi (C.B.Clarke)
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Erycibe malaccensis (C.B.Clarke)
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Erycibe micrantha (Hallier f.)
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Erycibe myriantha (Merr.)
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Erycibe nitidula (Pilg.)
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Erycibe obtusifolia (Benth.)
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Erycibe oligantha (Merr. & Chun)
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Erycibe paniculata (Roxb.)
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Erycibe papuana (Wernham)
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Erycibe pedicellata (Ridl. ex Hoogland)
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Erycibe peguensis (Prain)
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Erycibe praecipua (Prain)
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Erycibe puberula (Hoogland)
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Erycibe ramiflora (Hallier f.)
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Erycibe ramosii (Hoogland)
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Erycibe rheedei (Blume)
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Erycibe sangiheensis (Kochaiph. & Utteridge)
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Erycibe sapotacea (Hallier f. & Prain ex Prain)
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Erycibe sargentii (Merr.)
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Erycibe schlechteri (Pilg.)
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Erycibe schmidtii (Craib)
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Erycibe sericea (Hoogland)
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Erycibe sinii (F.C.How)
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Erycibe stapfiana (Prain)
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Erycibe stenophylla (Hoogl)
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Erycibe subglabra (Scheff. ex Hoogland)
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Erycibe subsericea (Hoogland)
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Erycibe subspicata (Wall. ex G.Don)
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Erycibe sumatrensis (Merr.)
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Erycibe terminaliflora (Elmer)
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Erycibe timorensis (Hallier f. ex Hoogland)
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Erycibe tixieri (Deroin)
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Erycibe tomentosa (Blume)
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Erycibe trichocarpa (Kochaiph. & Utteridge)
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Erycibe villosa (Forman)
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Erycibe zippelii (Hoogland)