The existence of a diurnal fluctuation in root metabolism can be deduced from several studies. While studying root respiration, Harris (13) noted a diurnal variation in the rate of CO2 production by roots of tomatoes and certain deciduous fruit trees. Cannon (5) found oxygen consumption of roots to be increased in light under conditions conducive to high transpiration. Grossenbacher (7) (16) believes may be associated with increased transpiration during the period of illumination. Went (26) observed that the accumulation of p32 in the shoots of tomato plants was more rapid during the day.These diurnal fluctuations in root activity could be a reflection of a diurnal variation in respiration rate, as suggested by the experiments of Harris (13). However, Grossenbacher (7) were propagated in a sand bed. After 4 weeks, uniformly rooted cuttings were transplanted to culture containers patterned after the root respiration apparatus described by White and Childers (27). Culture containers were 19-liter glass bottles with a 2.5 cm diameter hole drilled in the bottom. The bottles were inverted, filled with pea-sized gravel and the plant inserted through the hole. The woody stem of this species allowed the culture vessel to be completely sealed except for inlet and outlet tubes. Nutrient solution (Shive's R5C,, complete with iron and micronutrients) (21) was supplied by sub-irrigation. The containers were immersed in separate water baths which were controlled by individual thermostats to provide 15.6, 21.1, 26.7, and 32.2 C temperatures about the root systems. The shoots, however, were exposed to the normal greenhouse environment.Since the primary purpose of the Derris experiment was to study the long-term effect of root temperature on the synthesis of rotenone, the respiration studies were made just prior to harvest when the plants were 28 months old.Respiration measurements were made by periodically displacing the total volume of air from the gravel-filled bottles with nutrient solution. Aliquots of the displaced gas mixture were assayed for CO2 and 02 content by the procedure of Haldane (10). Measurements were made on duplicate plants for each of the four temperature treatments. Air samples were taken at 6-hour intervals, beginning at 6 AM for 5 days. Air volume was corrected to standard temperature and pressure.-