Genus Sindora in Subfamily Detarioideae
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!Sindora (Leguminosae: Detarioideae) is a medium-sized tropical genus of lowland forest trees with about 22 accepted species (POWO, 2024; WFO, 2024) and a Malesian distribution from southern Thailand and Peninsular Malaysia to Sumatra, Borneo, Java, the Philippines, and New Guinea (de Wilde, 1997). The type species is Sindora supa (Merrill) Merr. (de Wilde, 1997). Species are large, evergreen to semi-evergreen canopy trees; buds, young shoots, and inflorescences are typically invested in reddish to ferruginous indumentum. Leaves are paripinnate with a terminal, caducous or persistent tendril-like process; stipules are small, often caducous, and never large. Inflorescences are terminal or pseudoaxillary thyrses; flowers are marked by a conspicuous hypanthium and four petaloid lobes that close over the standard at maturity. The androecium is reduced to one fertile stamen; the remaining staminodes are short and petaloid, a diagnostic combination within Detarioideae. The ovary is usually 2-ovulate; placentation is apical-axile. Fruits are large, thick, woody, dehiscent pods typically bearing spiny or warty surfaces; each fruit produces one, rarely two, hard, exotestal seeds with a small, inconspicuous aril (de Wilde, 1997).
Diversity is concentrated in Borneo, with additional centers in Peninsular Malaysia and Sumatra (de Wilde, 1997). Most taxa occupy lowland to hill dipterocarp forests on well-drained soils; several extend into peat or kerangas forest and a few reach submontane belts (500–1,000 m). Endemism is high, especially in Borneo and the Philippines. Fossil pollen and leaf impressions link the genus to the Sundaland flora, reflecting biogeographic ties among these landmasses during Pleistocene sea-level fluctuations (Dick et al., 2003).
Ecologically, the solitary fertile stamen and tightly enclosed flower suggest a specialized pollination syndrome involving bees or hawkmoths (de Wilde, 1997). Pods are heavy and dehisce explosively, releasing the seed a short distance from the parent, consistent with limited ballistic dispersal; riparian S. inermis suggests occasional water transport (de Wilde, 1997). Base chromosome number is unknown.
Taxonomically, no widely recognized sectional or subgeneric framework has gained consensus; future molecular work is needed to test informal groups suggested by fruit morphology and geography (Brunei Forestry Department, 1999). Sindora is closely related to Afzelia and Koompassia, but retained in Sindora because of its distinctive floral reduction and single fertile stamen (Brunei Forestry Department, 1999; LPWG, 2017). Sindora supa remains the type and is treated as distinct from S. wallichii (de Wilde, 1997). World Flora Online (2024) lists 22 accepted species; Species 2000/ITIS (2024) records roughly 27–28 species, reflecting taxonomic lag.
Several species provide high-quality timber known as supa or sindora and are valued in construction and furniture; some, including S. supa, are widely cultivated and sometimes invasive in wetter sites outside their native range (de Wilde, 1997). Forest clearance, selective logging, and conversion have driven local declines, particularly of narrow endemics; conservation priorities include accurate red-list assessments and maintaining mixed dipterocarp habitats (de Wilde, 1997; Brunei Forestry Department, 1999).
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Sindora × changiensis (L.M.Choo, Loo, W.F.Ang & Er)
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Sindora affinis (de Wit)
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Sindora beccariana (Backer ex de Wit)
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Sindora bruggemanii (de Wit)
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Sindora coriacea (Prain)
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Sindora echinocalyx (Prain)
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Sindora galedupa (Prain)
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Sindora glabra (Merr. ex de Wit)
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Sindora inermis (Merr.)
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Sindora irpicina (de Wit)
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Sindora javanica ((Koord. & Valeton) Backer ex K.Heyne)
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Sindora klaineana (Pierre ex Pellegr.)
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Sindora laotica (Gagnep.)
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Sindora leiocarpa (Backer ex K.Heyne & de Wit)
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Sindora siamensis (Teijsm. ex Miq.)
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Sindora stipitata (Chatan & Promprom)
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Sindora sumatrana (Miq.)
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Sindora supa (Merr.)
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Sindora tonkinensis (A.Chev. ex K.Larsen & S.S.Larsen)
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Sindora velutina (Baker)
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Sindora wallichii (Benth.)