Perinuclear vesicles (estimated diameter less than 0.15 micron), too small to be seen in living mouse macrophages by direct phase-contrast microscopy, could be detected by darkfield microscopy thanks to their rapid non-saltatory movements at 37 degrees C, contrasting with the slower saltations of accompanying phase-visible larger vesicles (0.25-0.5 micron, presumed secondary lysosomes). The movements of these 'small visicles' also differed from those of the 'larger visicles' in their responses to changes in temperature, and to chemical agents known to inhibit both the saltations of secondary lysosomes and the latter's fusion with phagosomes. Thus the 'larger vesicles' stopped moving at 25 degrees C, the small ones did not; both stopped at 18 degrees C. The 'small vesicles' continued to move actively after cell uptake of the polyanion poly-D-glutamic acid, while the saltations of the 'larger vesicles' were markedly slowed; both sets of vesicles stopped after uptake of ammonium chloride. Degranulation of the small vesicles paralleled that of the larger, while simultaneously observed preformed pinosomes (labelled with fluorescent wheat germ agglutinin (WGA) appeared to be unaffected. On the basis also of refractivity, location and speed the 'small vesicles' are considered not to be pinosomes, but probably to be lysosomes. The question of whether they are a subgroup of small immature secondary lysosomes or primary lysosomes (0.05-0.08 micron) is discussed. The broad spectrum of movement inhibited by ammonia in macrophages raises the possibility that this weak base inhibits movements of all lysosomes. Further characterization of these 'small vesicles' requires their relation to be defined to the small particles in other cell types (especially in axoplasm) which have been detected by video-enhanced microscopy.