Abstract:A reliable method for producing reproductive cysts in Tetrahymena patula is described. The procedure involves the isolation of macrostomes without cytopharyngeal pouches in microdrops of distilled water under oil. The study of silver‐impregnated specimens has shown that a complex pattern of oral resorption and reformation occurs within the cyst that leads to the formation of a group of small cells with recessed oral apparatuses. These cells, called “cryptostomes,” swim very rapidly on excystment and are incapa… Show more
The functional mouth of exuviotrophic apostome ciltates appears only after an elaborate metamorphosis that begins at the onset of the molting of their crustacean hosts. In the tomite. a non‐feeding migratory stage, a mid‐ventrai depression at the origin of kineties x, y and z has been misidentified as the cytostome. Studies of fine structure and morphogenesis identify the true but nonfunctional cytostome—the subapiral lateral canal —and the falciform and ogival fields as the adoral ciliature. The anterior row of barren kinetosomes that parallels on the right the anterior third of the lateral canal is actually the infraciliature of a paroral. 2 rows of barren staggered kinetosomes. The canal itself is a narrow tube, its walls partially lined with microtubules. It begins 2–3 μm from the apex of the body and passes between falciform field 9 and the ogival field to end near the end of the ogival field. The fine structure of the infraciliature of the falciform and ogival fields differs markedly from that of the somatic kineties. In the host's early pre‐molt stages, the paroral migrates across the ventral surface of the encysted phoront and is accompanied by the microtubules of the lateral canal. The anterior end of falciform field 9 disorganizes into scattered kinetosomes, the trophont's anterior field of kinetosomes, but the posterior end migrates in an arc across the anterior ventral surface and remains as kinety a located near the angle where kinety 1 sharply par ra continues posteriad ind dorsad to the posterior limit of the extended cytostome. At the end of metamorphosis it sinks into The cytoplasm and disappears. The completion of the extended cytostome, the functional mouth, marks the termination of the microstome‐macrostome transformation. The fine structure of the infraciliature and microtubular elements making up the macrostome and the evocation of the microstome‐macrostome transformation in the presence of specific foods suggest that apostome ciliates any more properly be a suborder of Hymenostomatida rather than a subclass of Oligohymenophorea.
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