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~ Loganiaceae sensu lato
Habit and leaf form. Erect or straggling shrubs (or undershrubs), or lianas. Self supporting, or climbing; the climbers stem twiners. Leaves opposite, or whorled; ‘herbaceous’; petiolate; connate to not connate; simple. Lamina entire; pinnately veined (?). Leaves stipulate to exstipulate (often reduced to an interpetiolar line). Stipules interpetiolar to intrapetiolar (sometimes reduced to a stipular sheath joining the opposite leaf bases); with colleters. Lamina margins obscurely sinuate dentate, or entire. Domatia occurring in the family (in Coinochlamys (= Mostuea)); manifested as pockets.
Leaf anatomy. Extra-floral nectaries absent. Hairs present; eglandular. Complex hairs absent. The crystals without raphides.
Axial (stem, wood) anatomy. Young stems cylindrical. Internal phloem present. Secondary thickening anomalous. The anomalous secondary thickening from a single cambial ring. Primary medullary rays very wide (Gelsemium), or narrow (Mostuea).
The wood ring porous. The vessel end-walls simple (mostly), or reticulately perforated, scalariform, and simple (but then mostly simple). The vessels with vestured pits (Mostuea), or without vestured pits (Gelsemium). The axial xylem with fibre tracheids; without libriform fibres; including septate fibres, or without septate fibres. The parenchyma paratracheal (Gelsemium, or absent in Mostuea). ‘Included’ phloem present. The wood not storied.
Reproductive type, pollination. Unisexual flowers absent. Plants hermaphrodite; nearly always heterostylous.
Inflorescence, floral, fruit and seed morphology. Flowers aggregated in ‘inflorescences’; in cymes and in panicles. The ultimate inflorescence units cymose. Inflorescences terminal, or axillary (in one axil); with involucral bracts (two, basally united, in Coinochlamys), or without involucral bracts. Flowers bracteate (bracts variously shaped); one to many bracteolate; medium-sized to large (larger in Gelsemium); fragrant (at least in Gelsemium), or odourless (?); regular; 4 merous (occasionally, in Mostuea), or 5 merous (usually); cyclic; tetracyclic. Free hypanthium absent. Hypogynous disk absent.
Perianth with distinct calyx and corolla; 8, or 10; 2 whorled; isomerous. Calyx 4 (ocasionally), or 5; 1 whorled; polysepalous (Gelsemium), or gamosepalous (Mostuea); blunt-lobed, or toothed. Calyx lobes when gamosepalous, markedly shorter than the tube to about the same length as the tube. Calyx regular; ‘mostly’ persistent; non-accrescent; imbricate; when K5, with the median member anterior. Corolla 4 (rarely, in Mostuea), or 5; 1 whorled; gamopetalous; imbricate; funnel-shaped (the tube much longer than the lobes); more or less regular; white, or yellow, or orange, or red, or blue (or lilac).
Androecium 4 (rarely, in Mostuea), or 5. Androecial members adnate (inserted at the middle of the corolla tube or below); all equal, or markedly unequal (short-styled Mostuea flowers); free of one another; 1 whorled. Stamens 4 (rarely), or 5; inserted near the base of the corolla tube, or midway down the corolla tube; isomerous with the perianth; oppositisepalous; alternating with the corolla members; filantherous, or with sessile anthers (? — the filaments very short). Filaments not appendiculate. Anthers separate from one another, or connivent; dorsifixed; dehiscing via longitudinal slits; latrorse; unappendaged. Pollen grains aperturate; 3 aperturate; colporate.
Gynoecium 2 carpelled. Carpels reduced in number relative to the perianth. The pistil 2 celled. Gynoecium syncarpous; synovarious to synstylovarious (the style bifid, its branches bifid again); superior. Ovary 2 locular (glabrous or hairy). Gynoecium median. Ovary sessile. Gynoecium stylate. Styles 1–2; free to partially joined; apical. Stigmas 2, or 4 (each bifurcated); 4 lobed (twice dichotomously divided). Placentation axile (the placentas not bilobed). Ovules differentiated; 2 per locule (Mostuea), or 2–8 per locule (to ‘several’: Gelsemium); collateral (in 2–4 series); anatropous, or amphitropous (?); unitegmic. Outer integument contributing to the micropyle. Endothelium not differentiated. Hypostase absent.
Fruit non-fleshy; dehiscent; a capsule. Capsules septicidal, loculicidal, and valvular. Fruit 1–6 seeded (to ‘several). Seeds endospermic (endosperm starchy or bony); conspicuously hairy, or not conspicuously hairy (but no hair tuft); flattened, winged (Gelsemium), or wingless. Cotyledons 2. Embryo straight, or curved. Testa smooth, or hairy.
Physiology, phytochemistry. Alkaloids present. Verbascosides not detected. Iridoids detected; ‘Route I’ type (normal and seco, and complex indole alkaloids in both Mostuea and Gelsemium).
Geography, cytology. Holarctic, Paleotropical, and Neotropical. Eastern Asia, North and Central America, northern South America, Africa, Madagascar. 2n= 8, 16 (Gelsemium) and 20 (Mostuea. Supposed basic chromosome number of family: 4 and 10. Ploidy levels recorded: 2 and 4.
Taxonomy. Subclass Dicotyledonae; Tenuinucelli. Dahlgren’s Superorder Gentianiflorae; Gentianales. Cronquist’s Subclass Asteridae; Gentianales. APG III core angiosperms; core eudicot; Superorder Asteranae; lamiid. APG IV Order Gentianales.
Species 11. Genera 2; Gelsemium, Mostuea.
General remarks. See Leeuwenberg 1980, under Loganiaceae. Perhaps justifiably removed from Loganiaceae sensu lato by Struwe et al. (1994). They made no effort, however, to organize family descriptive data to the standards required for this package (see comment under Loganiaceae). On the basis of the much extended description given here, these genera are nearer to Gentianaceae than to Rubiaceae and Apocynaceae. See comments under Loganiaceae.
Illustrations. • Mostuea surinamensis: Hook. Ic. Pl. 12 (1876). • Gelsemium sempervirens: Köhler’s Medizinal-Pflanzen 3 (1898). • Gelsemium sempervirens: Bot. Mag. 128 (1902).
We advise against extracting comparative information from the descriptions. This is much more easily achieved using the DELTA data files or the interactive key, which allows access to the character list, illustrations, full and partial descriptions, diagnostic descriptions, differences and similarities between taxa, lists of taxa exhibiting or lacking specified attributes, distributions of character states within any set of taxa, geographical distribution, genera included in each family, and classifications (Dahlgren; Dahlgren, Clifford, and Yeo; Cronquist; APG). See also Guidelines for using data taken from Web publications.
Cite this publication as: ‘Watson, L., and Dallwitz, M.J. 1992 onwards. The families of flowering plants: descriptions, illustrations, identification, and information retrieval. Version: 25th April 2024. delta-intkey.com’.
