The families of flowering plants.
IncludingCleomaceae Horan. (p.p.)Excluding Cleomaceae, Koeberliniaceae,Pentadiplandraceae, Physenaceae, Setchellanthaceae
Habit and leaf form. Trees, or shrubs, or lianas, or herbs (rarely); non-glandular, not resinous. ‘Normal’ plants. Self supporting, or climbing. Xerophytic (commonly), or mesophytic. Leaves alternate; spiral, or distichous (rarely); petiolate; non-sheathing; gland-dotted, or not gland-dotted; simple, or compound; when compound, palmate. Lamina when simple dissected, or entire; when simple/dissected, palmatifid. Leaves stipulate, or exstipulate (stipules small). Stipules (when present) often spiny (or represented by glands). Lamina margins often involute. Leaves without a persistent basal meristem.
Leaf anatomy. Abaxial epidermis papillose, or not papillose. Stomata present; anomocytic. Hairs present; mostly eglandular (by contrast with Cleomaceae); unicellular and multicellular. Complex hairs present, or absent; peltate, or stellate, or capitate.
Adaxial hypodermis present, or absent. Lamina dorsiventral to centric. The mesophyll with sclerencymatous idioblasts, or without sclerenchymatous idioblasts. Minor leaf veins without phloem transfer cells (Capparis, Steriphoma).
Stem anatomy. Cork cambium present; initially deep-seated, or superficial. Nodes unilacunar. Cortical bundles (secondary, pericyclic) present, or absent. Medullary bundles absent. Internal phloem absent. Secondary thickening developing from a conventional cambial ring, or anomalous; via concentric cambia (often), or from a single cambial ring. The secondary phloem stratified into hard (fibrous) and soft (parenchymatous) zones, or not stratified. ‘Included’ phloem present (often), or absent. Xylem with fibre tracheids, or without fibre tracheids; with libriform fibres. Vessel end-walls simple. Vessels with vestured pits. Wood partially storied; parenchyma paratracheal. Sieve-tube plastids P-type, or S-type; when P-type type I (b).
Reproductive type, pollination. Plants hermaphrodite, or dioecious. Pollination entomophilous.
Inflorescence, floral, fruit and seed morphology. Flowers aggregated in ‘inflorescences’; usually in racemes. The ultimate inflorescence unit racemose. Inflorescences usually in racemes. Flowers bracteate; ebracteolate; regular to somewhat irregular; usually 4 merous. Floral receptacledeveloping a gynophore, or developing an androphore and developing a gynophore (causing the pistil to project). Hypogynous disk present; of separate members (a ring).
Perianthwith distinct calyx and corolla; (4–)6 (rarely), or 8; 2–4 whorled (more or less resolvable into K2+2 and C4 with decussate calyx and diagonal petals, cf. Cruciferae). Calyx 4 (2+2); 2 whorled; basally gamosepalous, or polysepalous. Calyx lobes about the same length as the tube, or markedly longer than the tube. Calyx bilabiate, or regular; imbricate.Corolla 4 (diagonal, very rarely 2); 1 whorled; not appendiculate; polypetalous (the petals equal or unequal, sometimes hooding).
Androecium basically 4, or 6–100 (i.e. to ‘many’, when branched). Androecial members branched (commonly), or unbranched; when branched, maturing centrifugally; free of the perianth; all equal to markedly unequal; basally coherent, or free of one another. The androecial bundles when detectable alternating with the corolla members. Androecium exclusively of fertile stamens, or including staminodes (or with staminodal branches). Stamens 4, or 6–20(–100) (to ‘many’); not didynamous, not tetradynamous; isomerous with the perianth to diplostemonous to polystemonous; basically oppositisepalous; filantherous, or petaloid and filantherous. Anthers dorsifixed to basifixed; dehiscing via longitudinal slits; introrse; tetrasporangiate. Endothecium developing fibrous thickenings. Anther epidermis persistent. Microsporogenesis simultaneous. The initial microspore tetrads tetrahedral, or decussate. Anther wall initially with more than one middle layer. Tapetum glandular. Pollen grains aperturate; (2–)3(–4) aperturate; colporate (colporoidate); 2-celled.
Gynoecium 2 carpelled, or 10–12 carpelled (by dédoublement). The pistil 1 celled, or 2 celled, or 3–12 celled. Gynoecium syncarpous; eu-syncarpous;superior. Ovary 1 locular (usually), or 2 locular (by false septa). Locules secondarily divided by ‘false septa’, or without ‘false septa’. Gynoecium when G=2 transverse. Ovary generally stipitate. Gynoecium non-stylate, or stylate. Styles 1; attenuate from the ovary; apical; shorter than the ovary. Stigmas 1; dorsal to the carpels, or commissural (?); dry type; papillate, or non-papillate; Group II type. Placentation when unilocular, parietal; when bilocular, parietal (without a ‘replum’, by contrast with Cleomaceae and Cruciferae). Ovules in the single cavity 10–100 (‘many’); when bilocular, 30–50 per locule (‘many’); arillate, or non-arillate; anatropous to campylotropous; bitegmic; crassinucellate. Outer integument contributing to the micropyle, or not contributing to the micropyle. Embryo-sac development Polygonum-type. Polar nuclei fusing prior to fertilization. Antipodal cells formed; 3; not proliferating; ephemeral (usually small, large in Maerua). Synergids hooked (sometimes with filiform apparatus). Endosperm formation nuclear. Embryogeny onagrad, or solanad.
Fruit fleshy, or non-fleshy; dehiscent, or indehiscent; a capsule (often), or a berry (usually), or a drupe, or a nut, or a samara. Capsules sometimes valvular (resulting in two valves to which the placentas remain attached — i.e., no replum). Seeds endospermic, or non-endospermic. Cotyledons 2 (oily). Embryo variously curved, or bent. The radicle lateral, or dorsal.
Physiology, biochemistry. Mustard-oilspresent. Cyanogenic, or not cyanogenic. Alkaloids present (21 species). Iridoids not detected. Proanthocyanidins absent. Flavonols absent. Ellagic acid absent (Euadenia). Aluminium accumulation not found. C3. C3 physiology recorded directly in Cadaba, Capparis, Maerua. Anatomy non-C4 type (Boscia, Capparis).
Geography, cytology. Temperate to tropical. Widespread. X = 10, 11, 17.
Taxonomy.Subclass Dicotyledonae; Crassinucelli. Dahlgren’s Superorder Violiflorae; Capparales. Cronquist’s Subclass Dilleniidae; Capparales. APG 3 core angiosperms; core eudicot; Superorder Rosanae; malvid; Order Brassicales.
Species 650. Genera about 25; Apophyllum, Bachmannia, Belencita, Borthwickia,Boscia, Buchholzia, Cadaba, Capparis, Cladostemon,Crateva, Dactylaena, Dipterygium (or Cruciferae?), Euadenia,Forchhammeria, Maerua, Morisonia, Neothorelia, Podandrogyne,Poilanedora(?), Puccionia (or Cruciferae?), Ritchiea, Steriphoma,Stixis, Thilachium, Tirania.
General remarks. Separation from Cleomaceae may be unsustainable, since difficulties are encountered in assigning the genera. Precise comparative data on gynoecium and fruit structure are elusive or non-existent.
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