Embryonic lens vesicles from both species of salamander self-diff erentiated into a small lens with fibers when implanted into either the dorsal f i n or anterior chamber of the larval eye. Growth of these lenses was very slow in Amblystoma and somewhat faster in Triturus. When implanted into the pupil in place of the extirpated host lens, the embryonic lens vesicles differentiated normally and had a normal rate of growth. Lens regeneration from the host iris in Triturus was frequently inhibited by the implanted lens. A statistical analysis by the method of covariance showed that, in both species, lenses from the implants were largest in the lentectomized eyes, smaller in the vitreous chamber of eyes with intact host lens and smallest in the anterior chamber, host lens present. In Amblystma, the growth rates, as indicated by the coefficients for linear regression, were significantly different between lenses developing in the absence of the host lens and those growing from implants into either the anterior or vitreous chambers of eyes containing the host lens. In Trituru.~, a significant difference was observed only between growth rates of lenses in the lentectomized eyes and in the anterior chambers, host lens present or in the dorsal fin. These results show that the neural retina stimulates growth and differentiation of embryonic lens vesicles and that the host lens retards their growth.The regeneration of a lost part in an older animal frequently repeats many of the events of morphogenesis and cytodifferentiation that characterized the development of this structure during embryonic Iife. However, this takes place in an environment which is quite different from that found in an embryo. Unlike the embryonic anlage, the regenerating part is subject to local influences from adjacent differentiated tissues and to systemic influences such as hormones. The interactions of these factors have been extensively investigated in the many studies on regeneration of the amphibian limb. The regeneration of a lens from the pigmented epithelium of the dorsal iris in certain urodeles also repeats the events of morphogenesis and histogenesis observed in the embryonic development of the lens from the surface ectoderm overlying the optic vesicle and cup. In the embryo, lens development is stimulated and modu- namely, the entoderm of the dorsal-antenor archenteron wall, the adjacent mesoderm and, finally, the optic vesicle and cup (Liedke, '51, '55; Reyer, '58a, b; Jacobson, '55, '58, '63a, b, c). In the larval and adult eye, the presence of the neural retina is essential for the initiation of lens regeneration from the iris (reviewed by Stone, '59, '65; Goss, '64; Reyer, '54, '62a). This is normally released by extirpation of the host lens. It was of interest, therefore, to test the response of the prospective lens-forming ectoderm and embryonic lens vesicle to the environment of the differentiated eye, especially to any influences emanating from the host neural retina or lens. Experiments have already been reported (Reyer...