Genus Trigonotis in Family Boraginaceae
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!Trigonotis is a genus of Boraginaceae comprising approximately 140 species of low, herbaceous plants whose main diversity lies in East Asia and the Sino‑Himalayan region, with secondary centers in Japan, Korea, the Russian Far East, and isolated outliers in the Himalaya. The type species is T. peduncularis (A. DC.) Benth. ex C.B. Clarke (POWO, 2024; WFO, 2024). Plants typically form basal rosettes and bear dichasial cymes; leaves are usually soft-pubescent, and although stipules are absent, the indumentum frequently includes bristly hairs. The rotate to broadly campanulate corolla has five, well‑exserted stamens inserted below a throat appendage with short scales or folds; the ovary is deeply four‑lobed with a single pendulous ovule per lobe, and the fruit is a schizocarp of ovoid, dorsiventrally flattened mericarps. This combination of planar mericarps with a conspicuous annular throat scale in the corolla distinguishes Trigonotis from closely related members of Boraginaceae (Luebert et al., 2016; Miller et al., 2021).
Species richness is highest in southwestern China and the Himalaya, where several endemics occur on moist cliffs, stream banks, forest margins, and alpine meadows from lowlands to about 3500 m. The flora of eastern China and Japan contributes numerous narrow endemics, and the group exhibits typical Sino‑Himalayan disjunction patterns (Chen et al., 2011). Flowers are reported as entomophilous and visited by small flies and bees; fruit dispersal appears primarily by gravity and secondary epizoochory following mericarp attachment, though quantitative studies remain sparse (F. Zhao et al., 2018). Chromosome counts are predominantly 2n=18, consistent with x=9 as the probable base number (F. Zhao et al., 2018), although broader sampling is needed.
Recent work supports placement of Trigonotis in tribe Cynoglosseae and recognizes two informal clades corresponding to the East Asian and Sino‑Himalayan radiations; no formal infrageneric classification is broadly applied, although subgeneric names such as subg. Trigonotis and subg. Koma have appeared historically (Luebert et al., 2016; Miller et al., 2021). Boundaries with formerly segregated taxa such as Komatina remain unsettled in some treatments (Miller et al., 2021). The genus is chiefly horticultural rather than economic; a few species, notably T. peduncularis, are cultivated in East Asia for their early, bright blue flowers, but no major crops or timber sources are associated with the group. Although no invasive Trigonotis is widely recognized, localized weedy occurrences near settlements exist. Habitat conversion, overgrazing, and collection pressure threaten several narrowly distributed taxa, and targeted field surveys, genetic diversity assessments, and phylogenomic resolution are needed to guide future conservation actions (Chen et al., 2011; Miller et al., 2021).
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Trigonotis abata (I.M.Johnst.)
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Trigonotis apoensis (Elmer)
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Trigonotis barkamensis (Ching J.Wang)
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Trigonotis borneensis ((Stapf) I.M.Johnst.)
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Trigonotis bracteata (Ching J.Wang)
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Trigonotis caespitosa (S.P.Banerjee)
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Trigonotis cavaleriei ((H.Lév.) Hand.-Mazz.)
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Trigonotis chengkouensis (W.T.Wang)
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Trigonotis ciliolata (I.M.Johnst.)
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Trigonotis cinereifolia (Ching J.Wang)
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Trigonotis clarkei (R.R.Mill)
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Trigonotis compressa (I.M.Johnst.)
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Trigonotis corispermoides (Ching J.Wang)
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Trigonotis culminicola (P.Royen)
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Trigonotis delicatula (Hand.-Mazz.)
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Trigonotis doormanensis (B.Xue)
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Trigonotis floribunda (I.M.Johnst.)
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Trigonotis formosana (Hayata)
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Trigonotis funingensis (H.Chuang)
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Trigonotis giraldi (Brand)
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Trigonotis giraldii (Brand)
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Trigonotis gracilipes (I.M.Johnst.)
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Trigonotis guilielmi ((A.Gray) Gürke)
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Trigonotis haackei (F.Muell.)
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Trigonotis harrysmithii (R.R.Mill)
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Trigonotis heliotropifolia (Hand.-Mazz.)
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Trigonotis hirsuta (Steenis)
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Trigonotis hookeri (Benth. ex C.B.Clarke)
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Trigonotis icumae (Makino)
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Trigonotis inoblita (F.Muell.)
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Trigonotis jinfoshanica (W.T.Wang)
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Trigonotis laxa (I.M.Johnst.)
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Trigonotis leucantha (W.T.Wang)
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Trigonotis leyeensis (W.T.Wang)
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Trigonotis longipes (W.T.Wang)
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Trigonotis longiramosa (W.T.Wang)
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Trigonotis macrophylla (Vaniot)
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Trigonotis mairei ((H.Lév.) I.M.Johnst.)
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Trigonotis microcarpa (Benth. ex C.B.Clarke)
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Trigonotis minuta (I.M.Johnst.)
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Trigonotis mollis (Hemsl.)
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Trigonotis muliensis (W.T.Wang)
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Trigonotis myosotidea (Maxim.)
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Trigonotis nandanensis (Ching J.Wang)
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Trigonotis nankotaizanensis ((Sasaki) Masam. & Ohwi)
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Trigonotis omeiensis (Matsuda)
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Trigonotis opaca ((I.M.Johnst.) I.M.Johnst.)
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Trigonotis orbicularifolia (Ching J.Wang)
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Trigonotis ovalifolia (Benth. ex C.B.Clarke)
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Trigonotis papuana ((Hemsl.) I.M.Johnst.)
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Trigonotis peduncularis (Steven ex Palib.)
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Trigonotis petiolaris (Maxim.)
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Trigonotis philippinensis (Merr.)
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Trigonotis pleiomera (I.M.Johnst.)
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Trigonotis procumbens ((Warb.) I.M.Johnst.)
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Trigonotis radicans (Steven)
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Trigonotis robusta ((I.M.Johnst.) I.M.Johnst.)
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Trigonotis rockii (I.M.Johnst.)
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Trigonotis rotundata (I.M.Johnst.)
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Trigonotis rotundifolia (Benth. ex C.B.Clarke)
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Trigonotis smithii (S.P.Banerjee)
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Trigonotis subrosulata (Riedl)
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Trigonotis tenera (I.M.Johnst.)
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Trigonotis tibetica (I.M.Johnst.)
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Trigonotis vestita (I.M.Johnst.)
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Trigonotis zhuokejiensis (W.T.Wang)