Using leaf epidermis from Vicia faba, we tested whether auxin-induced stomatal opening was initiated by auxin-induced ethylene synthesis. Epidermis was dark-incubated in buffered KNO3 containing 0.1 mM alpha -napthalene acetic acid or 1 mM indole-3-acetic acid. Maximum net opening was ca, 4 mum after 6 h. Opening was reversed by 20 muM ABA, 0.1 mM CaCl2. 1-Aminocyclopropane carboxylic acid (ACC) synthase catalyzes synthesis of ACC, the immediate precursor to ethylene, Auxin-induced stomatal opening was fully inhibited by 10 muM 1-aminoethoxyvinylglycine (AVG), an ACC synthase inhibitor, In solutions containing AVG, auxin-induced opening was restored in a concentration-dependent manner by exogenous ACC, but not in control solutions lacking an auxin, ACC-mediated reversal of AVG-inhibition of stomatal opening was inhibited by a-aminoisobutyric acid (AIB), an inhibitor of ACC oxidase, the last enzyme in the ethylene biosynthetic pathway, by 10 muM silver thiosulfate (STS), an inhibitor of ethylene action, and by 20 muM ABA, 0.1 mM CaCl2, CoCl2, an inhibitor of ethylene synthesis, also inhibited auxin-induced opening. Both STS and CoCl2, inhibited opening induced by light or by fusicoccin, but neither light- nor fusicoccin-induced opening was inhibited by AVG. These results support the hypothesis that auxin-induced stomatal opening is mediated through auxin-induced ethylene production by guard cells.