Family Barringtoniaceae
Reproductive type, pollination. Plants hermaphrodite. Inflorescence, floral, fruit and seed morphology. Flowers solitary, or aggregated in ‘inflorescences’ (usually); when solitary, terminal; in racemes, or in corymbs. The ultimate inflorescence unit racemose. Inflorescences terminal, or axillary; racemes or corymbs, often elongated. Flowers medium-sized to large; regular to very irregular; when irregular, asymmetric. The floral irregularity involving the androecium, or involving the perianth and involving the androecium. Flowers cyclic; pentacyclic, or polycyclic. Free hypanthium present to absent. Perianth with distinct calyx and corolla; (6–)8–12; 2 whorled; isomerous; different in the two whorls. Calyx (2–)4(–6); 1 whorled; polysepalous, or gamosepalous; when gamosepalous, blunt-lobed; calyptrate (rarely, in Barringtonia), or not calyptrate; imbricate (rarely calyptrate). Corolla 4(–6); 1 whorled; polypetalous, or gamopetalous (sometimes fused to the staminal cup); imbricate. Androecium 50–100 (or more — i.e. ‘many’, giving the flowers a fluffy, myrtaceous appearance). Androecial members maturing centrifugally; free of the perianth, or adnate (to the corolla); coherent (the filaments basally united, usually in several series, often concentrated on one side of the flower by abortion of members); 1–20 adelphous (to ‘polyadelphous’); 3–5 whorled (‘in several series’). Androecium exclusively of fertile stamens, or including staminodes (sometimes including members lacking anthers). Stamens 20–100 (‘many’); polystemonous; inflexed in bud (or incurved). Anthers basifixed; dehiscing via longitudinal slits; latrorse; tetrasporangiate. Endothecium developing fibrous thickenings. Microsporogenesis simultaneous. Anther wall initially with more than one middle layer (two); of the ‘basic’ type. Tapetum amoeboid. Pollen grains aperturate; 3 aperturate (with a specialised marginal ridge); (syn-) colpate, or colporate (or colporoidate); 3-celled. Gynoecium 2–4(–6) carpelled. Carpels reduced in number relative to the perianth to isomerous with the perianth. The pistil 2–4(–6) celled. Gynoecium syncarpous; eu-syncarpous; inferior. Ovary 2–4(–6) locular. Epigynous disk present (intrastaminal). Gynoecium stylate. Styles 1; apical. Stigmas 1. Placentation axile to apical. Ovules 2–50 per locule (to ‘many’); anatropous; unitegmic (?—Cronquist 1981), or bitegmic; tenuinucellate. Outer integument not contributing to the micropyle. Embryo-sac development Polygonum-type. Endosperm formation nuclear. Fruit fleshy, or non-fleshy; dehiscent, or indehiscent; capsular-indehiscent (then broadly 4-winged), or a berry (then fibrous, usually one-seeded), or a capsule. Capsules sometimes circumscissile. Seeds non-endospermic; often woody and large. Embryo well differentiated. Physiology, biochemistry. Iridoids not detected. Proanthocyanidins absent. Geography, cytology. Paleotropical. Tropical. Palaeotropical. X = 13. Taxonomy. Subclass Dicotyledonae; Tenuinucelli. Dahlgren’s Superorder Theiflorae; Theales. Cronquist’s Subclass Dilleniidae; Lecythidales. APG (1998) Eudicot; core Eudicot; Asterid; unassigned to Euasterid I or Euasterid II. APG 3 (2009) Order: Ericales. Species about 55. Genera 6; Abdulmajidia, Barringtonia, Careya, Chydenanthus, Combretodendron (= Petersianthus), Petersianthus, Planchonia. Morton et al. (1998) present these genera as subfamily Planchonioideae of an expanded Lecythidaceae, based on an assessment ‘using both molecular and morphological data’. |