Endogenous peroxide levels in pear fruit (Pyrus communis) were measured using a titanium assay method, and were found to increase during senescence in both Bartlett and Bosc varieties. Application of glycolic acid or xanthine, serving as substrates for the formation of H202, increased the peroxide content of the tissue and accelerated the onset of ripening, as measured by increased softening and ethylene evolution. Application of ethylene also induced increased peroxide levels. Ripening processes were similarly promoted when peroxides were conserved by inhibiting the activity of catalase with hydroxylamine or potassium cyanide. By comparison, the inhibition of glycolate oxidase with alphahydroxy-2-pyridinemethanesulfonic add decreased the peroxide content of the tissue and delayed the onset of ripening. These results indicate that the onset of ripening correlates with the peroxide content of fruit tissues as occurring under normal conditions or as influenced by the treatments. Hydrogen peroxide may be involved in oxidative processes required in the initiation and the promotion of ripening.Fruit ripening is viewed as an oxidative phenomenon (3, 5), as indicated by results suggesting the decline in sulfhydryl gradients during ripening (7) and the acceleration of ripening processes by the application of high 02 tensions (2, 5, 10). We hypothesize that the effects of 02 reflect, in part, the utilization of 02 for the formation of peroxides for the following reasons.a. The free radical theory of aging proposes that progressive aging results from the random and cumulative attack by oxygen radicals (partially reduced oxygen forms) (16). However, the view of ripening as a regulated senescence phenomenon (13) requires a controlled turnover of radicals. Hydrogen peroxide is a stable partially reduced oxygen form (15), and its turnover is characteristically mediated by enzyme action. For that reason, we envision that H202 can be integrated into the regulated metabolic events occurring during senescence in fruit.b. The acceleration of ripening by high 02 tensions (6, 10) is consistent with the high Km(02) of some peroxide-forming enzyme systems (26).c. The onset of senescence in some systems is accompanied by an increase in the activity of peroxide-utilizing enzymes (4) and a decrease in peroxide-destroying enzymes (17).In the present work, we found that changes in peroxides, as The treated fruit were kept at 21 C at standard conditions and ventilated with air at a rate of 400 ml/min. Ethylene was scrubbed from the ventilating air with Purafil (H. E. Burrough and Assoc., Chamblee, Ga.).Fruits were sampled at intervals for measuring the rate of softening, ethylene evolution, and peroxide levels. Softening and peroxides were measured at 0, 2, 4, 6, and 8 days following infiltration. Ethylene evolution was measured daily for the duration of the experiment. Samples of 10 fruit were used for each of the above determinations. All determinations were run in duplicate. Ethylene was collected from the ventilating gases accor...