DURING THE course of an earlier investigation, Albaum and Commoner (19,1<1) were able to show that iodoacetic acid inhibited the growth of intact oat seedlings. This inhibition, however, did not appear immediately, but was manifest only after the seedlings had been subjected to the treatment for several days. At the time it was assumed that this lag in response might be due to difficulty in penetration of the iodoacetate. Subsequent experiments with other respiratory poisons and some stimulants, however, made this explanation highly unlikely. These new experiments indicated that iodoacetate, and some of the respiratory stimulants used, produced no immediate effects on growth because the .early growth stages are probably under the control of metabolic processes insensitive to these substances, but with time new metabolic mechanisms appear which respond to the addition of these substances. This paper amplifies the results of some of these later experiments and presents more complete evidence establishing the operation of at least two distinct respiratory mechanisms controlling the growth of the oat seedling.:MATERIAL AND METHoDs.-Grains of Avena sativa L. var. Black Norway, similar to those used in earlier experiments were hulled, soaked in distilled water for two hours in the light, and germinated in the dark for twenty-four hours at 27°C. After germination, the grains were planted in beakers in contact with moist filter paper, as described in an earlier paper (Kaiser and Albaum, 1939), to which test solutions had been added. The plants were then allowed to continue their growth in the dark at the same temperature. At regular intervals, the coleoptiles were measured to the nearest millimeter. Coleoptile length was used as an index of growth. All figures reported are the averages of at least twenty plants. The test solutions, iodoacetic, fumaric, pyruvic, succinic, malic, maleic and malonic acids, and sodium azide (all Eastman Kodak) were made up in distilled water and adjusted with a Beckmann pH meter to pH 6.0 with KOH at the beginning of each experiment. The pH of these solutions did not change appreciably during the course of the experiments.All measurements on oxygen uptake were carried out in a Warburg respirometer at 26°C. Those experiments not performed on intact embryos (prepared by dissection from seedlings; see below) were carried out on extracts made up in the following way: Grains were removed from beakers in which they had been grown, 24, 48, 72, 96 and 120 hours after soaking. The embryos were carefully dissected from groups of fifty seedlings, ground in sand in 2 cc. of