Larvae of Rana chensinensis developed from fertilized eggs which had been subjected to ultraviolet (u.v.) irradiation on their vegetal hemisphere at a dose of 20000 ergs/mm2 within 60 min of fertilization contained no primordial germ cells (PGCs) when examined histologically at the stage when the operculum was complete (8 days after fertilization at 18 °C, stage 25 according to Shumway, 1940). The morphogenetic ability of vegetal pole cytoplasm from non-irradiated eggs to establish the PGCs was tested by injecting some fractions of this cytoplasm into the vegetal hemisphere of u.v.-irradiated eggs. Crude homogenate of the vegetal pole cytoplasm without large yolk platelets was able to restore the PGCs when injected into u.v.-irradiated eggs, but a similar fraction from animal half cytoplasm had no ability to form PGCs. The ‘PGC-forming activity’ demonstrated in the crude homogenate of the vegetal pole cytoplasm was not abolished by dialysis, lyophilization and heating to 90 °C for 10 min. When the homogenate was fractionated by differential centrifugation in 0·25 M sucrose, the ‘PGC-forming activity’ was recovered mainly in the precipitate of 15000 g for 30 min. The precipitate of 7000 g for 10 min had also a little ‘activity’. The possibility was discussed that the ‘PGC-forming activity’ demonstrated in the vegetal pole cytoplasm was associated with the germinal granules in the germ plasm rather than the mitochondria.

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