| Contents | Classes | Subclasses | Orders |
Order 1. HETEROTRICHIDA Stein, 1859
| Syns. | Heterotricha, Heterotrichorida, Heterotrichorina |
With characteristics of subclass s.s. (above). Body generally large to very large, sometimes highly contractile; somatic ciliation frequently holotrichous, with regular, even dense, rows of simple cilia (though not true of all suborders); wide distribution, both free-living and symbiotic forms.
| With characteristics of order s.s. (above). Somatic ciliature well developed, but buccal organelles (paramembranelles) also numerous and prominent; of large body size, often contractile; single conspicuous contractile vacuole at posterior end of body; mucocysts in abundance, and pigment vesicles common in many species; no loricae, but cysts common; essentially all freeliving forms [endosymbiotic families formerly included here now comprise separate suborder: see below] , widely distributed in great variety of habitats. | Suborder (1) Heterotrichina Stein, 1859 |
| As in preceding suborder, somatic ciliature well developed, buccal organelles numerous and prominent (though here unique as heteromembranelles), and body size often above average (i.e., > 150 µm). But additionally, here, are kinetodesmal (as well as cathetodesmal and retrodesmal) fibers in some species; complex "systèmes sécants," characteristic of specific kinetal patterns; macronuclear karyophore in many species; sometimes conspicuous dorsoanterior sucker; cilia-lined cytoproct in several forms; and all species endosymbionts in digestive tract of either insects (or certain related arthropods) and lower vertebrates or, less often, in oligochaetes and molluscs. | Suborder (2) Clevelandellina de Puytorac & Grain, 1976 |
| Body generally small, top-shaped (often with very long caudal spine), with somatic ciliature absent except for caudal tuft and several anteriorly located cirri; buccal ciliature (accompanied by a "ciliary stripe") extensive, encircling body and spiraling posteriad, with cytostome thus near antapical pole; pellicle rigid; large ovoid macronucleus, multiple in several species; free living polysaprobic forms, typically in fresh-water habitats. | Suborder (3) Armophorina Jankowski, 1964 |
| Universally loricate, sessile forms, with vermiform migratory larval stage; body large and elongate, especially in neck region in some species, with conspicuous pair of "peristomial wings" extending from the lorica (a structure generally cylindrical, with a definite bend in some species) and bearing the prominent buccal ciliature; somatic ciliation uniform and holotrichous; body highly contractile and often pigmented; stomatogenesis parakinetal; widely distributed in marine habitats (few species, fresh-water), with loricae attached to algae, higher aquatic plants, or integument or shells of invertebrates (molluscs, various crustaceans, bryozoa, coelenterates, etc.). | Suborder (4) Coliphorina Jankowski, 1967 |
| Body laterally flattened, elongate-ovoid, with right side slightly concave; somatic ciliation uniform, but cilia in small, cirrus-like groups; no adhesive sucker; buccal ciliature extensive, coursing from apical end to subequatorial position; stomatogenesis parakinetal; macronucleus dendritic, with no karyophore; no mucocysts; endocommensals solely in certain species of lumbricid oligochaete annelids. | Suborder (5) Plagiotomina Albaret, 1974 |
| Body in form of hourglass, with prominent oral disc apically and conspicuous basal disc at posterior pole; essentially without cilia except for buccal organelles and posterior ciliary rings; stomatogenesis apokinetal; basal disc, fiber-rich and quite complex, serves as organelle of attachment; macronucleus moniliform or fragmented; ectocommensals on a variety of marine organisms ranging from an alga (substratum for one unique species) to tunicates, with coelenterates, annelids, molluscs, and echinoderms (sea cucumber) also involved. | Suborder (6) Licnophorina Corliss, 1957 |