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The families of flowering plants

L. Watson and M.J. Dallwitz

Theligonaceae Dum.

Alternatively Thelygonaceae auctt., Cynocrambaceae Nees; ~ Rubiaceae.

Habit and leaf form. Fleshy herbs (with more chloroplasts in the pith of the stem than in the cortex, and lacking mechanical tissue other than xylem). Plants somewhat succulent; green and photosynthesizing. Annual, or perennial; without conspicuous aggregations of leaves. Leaves opposite (below), or alternate (sometimes, above, by suppression of one member of each pair); fleshy; petiolate; simple. Lamina entire; pinnately veined, or palmately veined. Leaves stipulate. Stipules interpetiolar; with colleters (on the inside, near the tip). Lamina margins entire.

Leaf anatomy. The leaf lamina dorsiventral. Stomata present; on both surfaces (but more numerous abaxially); paracytic. Hairs present; glandular (club-shaped). The mesophyll containing crystals. The crystals exclusively raphides (in idioblasts).

Axial (stem, wood) anatomy. Primary vascular tissues in a cylinder, without separate bundles; collateral. Internal phloem absent. Secondary thickening developing from a conventional cambial ring.

The vessels small. The axial xylem with fibre tracheids, or without fibre tracheids (female flowers). ‘Included’ phloem absent.

Reproductive type, pollination. Plants monoecious. Gynoecium of male flowers absent. Pollination anemophilous.

Inflorescence, floral, fruit and seed morphology. Flowers solitary and aggregated in ‘inflorescences’ (the males mostly borne singly or paired opposite the leaves at the upper nodes, unless each ostensible ‘flower’ is interpreted as a cluster; the females mostly in simple axillary dichasia at the lower nodes). The ultimate inflorescence units cymose. Inflorescences axillary; mostly in 1–3 flowered cymes — assuming that what are ostensibly male flowers are not interpreted as inflorescences. Free hypanthium absent. Hypogynous disk absent.

Perianth ostensibly sepaline (in male flowers, where it is closed in bud, subsequently becoming valvately 2–5 partite with broad, revolute segments; unless the ‘perianth’ is here interpreted as an involucre surrounding a reduced flower cluster), or petaline (the female flowers with a membranous, oblique, tubular, 2–4 valvately toothed perianth, interpreted as a corolla); 2–5. Calyx of the male flowers, if so interpreted, 2–5 (partite); valvate. Corolla of female flowers, if so interpreted, 2–4 (toothed); gamopetalous; valvate; vase-shaped (produced above into a narrow tube); unequal but not bilabiate.

Androecium in male flowers, (2–)7–12(–30). Androecial members branched (i.e., perhaps thus interpretable), or unbranched; free of the perianth; free of one another, or coherent; sometimes 2–5 adelphous (the stamens sometimes in groups of 2, 4 or 6). Androecium exclusively of fertile stamens. Stamens (2–)7–12(–30); erect in bud (the anthers becoming pendulous at anthesis); filantherous (the filaments filiform). Anthers versatile; dehiscing via longitudinal slits; bilocular; tetrasporangiate. Microsporogenesis simultaneous. The initial microspore tetrads tetrahedral. Pollen grains aperturate; 4–8 aperturate; (brevi-) colpate to porate; 3-celled.

Gynoecium ostensibly 1 carpelled. The pistil 1 celled. Gynoecium ostensibly monomerous (but ‘really’ pseudomonomerous?); ostensibly of one carpel; superior. Carpel stylate; with a gynobasic style (this filiform, exserted from the mouth of the perianth); 1 ovuled. Placentation basal. Ovules non-arillate; campylotropous, or amphitropous; unitegmic (the integument massive); tenuinucellate (Wunderlich 1971). Endothelium not differentiated. Embryo-sac development Polygonum-type. Antipodal cells formed; 3; not proliferating; ephemeral. Endosperm formation nuclear. Embryogeny probably solanad.

Fruit non-fleshy. The fruiting carpel indehiscent; nucular, or drupaceous. Fruit 1 seeded (the seed hippocrepiform). Seeds endospermic. Endosperm oily. Cotyledons 2. Embryo strongly curved.

Seedling. Germination phanerocotylar.

Physiology, phytochemistry. Verbascosides not detected. Iridoids detected; ‘Route I’ type (normal). Betalains absent. Sieve-tube plastids S-type.

Geography, cytology. Holarctic. Temperate to sub-tropical. Canaries, Mediterranean, Southwest China, Japan. N = 10 or 11.

Taxonomy. Subclass Dicotyledonae; Tenuinucelli. Dahlgren’s Superorder Gentianiflorae; Gentianales. Cronquist’s Subclass Asteridae; Rubiales. APG III core angiosperms; core eudicot; Superorder Asteranae; lamiid. APG IV Order Gentianales (as a synonym of Rubiaceae).

Species 3. Genera 1; only genus, Theligonum.

General remarks. See Wunderlich 1971. Differing from Rubiaceae sensu stricto (q.v.) in succulence, perianth morphology, free androecium, (pseudo-)monomerous ovary with campylotropous or amphitropous ovules; also in records of xylem without tracheids and assumed absence of inulin.

Illustrations. • Le Maout and Decaisne: Theligonum cynocrambe. • Theligonum cynocrambe: Ic. florae Germanicae et Helveticae 24 (1909).

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: 15th April 2018.’.