Since the discovery of heavy water, many experiments have been made to determine its influence upon living organisms. Although some of these investigations have shown little effect (Melot, 1934;Rea and Yuster, 1934), others (Lewis, 1933;Harvey, 1934;Ussing, 1935) reported a depressing action on the growth of plants and animals. The pioneer experiment in this field was carried out by Lewis (1933). Tobacco seed (Nicotiana tabacum var. purpurea) would not germinate in 100 per cent heavy water but did germinate very slowly in a 50 per cent concentration. Pratt and Curry (1937) found that wheat seedlings and the lower parts of buds of Kalanchoe daigremontiana grew only 0.025 as rapidly in 99 per cent heavy water as in normal water. The osmotic effects of heavy water on the leaf cells of Nitella clavata was studied by Brooks (1937), who found that the cells shrank in heavy water and expanded in normalwater. It was concluded that heavy water was hypertonic to the cells.Fox, Cupp, and McEwen (1936) measured the growth of diatoms in 1 per cent heavy water and in filtered sea water. They reported a lag of 16 per cent in the growth rate of Nilzschia bilabata over a period of 12 days in heavy water. Freshly collected Spirogyra placed in 0.06 per cent heavy water by Barnes (1933) was characterized by lack of movement, much less cell disjunction, and greater longevity than the controls in distilled water. A study of the influence of heavy water upon the rate of photosynthesis was made by Craig and Trelease (1937) upon Chlorella vulgaris suspended in a carbonate-bicarbonate buffer. Using the evolution of oxygen as a measure of photosynthesis, they found a decrease in the rate of 0.41 in 99.9 per cent heavy water. Using the same organism, Pratt (1938) found the decrease in growth to be in inverse linear proportion to the concentration of deuterium oxide up to 75 per cent, at which concentration practically no growth occurred.Taylor, Swingle, Eyring, and Frost (1933) showed that 92 per cent of heavy water influenced the life processes of tadpoles, Rana clamitans; fish, Lebestes reticulatus; flatworms, Planaria maculata; and the protozoan, Paramecium caudatum. The tadpole died within an hour; the fish within 2 hours; the flatworm within 3 hours; but the Paramecium lived 48 hours. When the concentration was decreased to 30 per cent, no effect could be detected on the tadpoles, fish, or flatworms over a period of 48 hours. When the white mouse was subjected (Barbour, 1935) to a 99 per cent solution of heavy water, the metabolism was slowed