Stimulation of the stigma of Hibiscus flowers by pollen, wounding (heat), or cold shock (4°C) evokes electrical potential changes in the style, which propagate toward the ovary with a speed of 1.3 to 3.5 cm s-'. Potential changes were measured intracellularly by microelectrodes inserted i n the style. l h e resting potential ranged from -90 to -112 mV (n = 20) in cells of the vascular tissue and from -1 84 to -220 mV (n = 22) in cells of the pollen-transmitting tissue.The amplitude of the potential changes was between 40 and 150 mV, depending on the kind of stimulus. Self-as well as crosspollination hyperpolarized the resting potential after 50 to 100 s, followed by a series of 10 to 15 action potentials. I n contrast, cooling of the stigma caused a single action potential with a different shape and duration, whereas wounding generated a strong depolarization of the membrane potential with an irregular form and a lower transmission rate. To determine the physiological function of the different signals measured i n the style, the gas exchange and metabolite concentrations were measured in the ovary before and 1 O min after stimulation of the stigma. Self-and cross-pollination caused a transient increase of the ovarian respiration rate by 12%, which was measured 3 to 5 min after the stigma was stimulated. Simultaneously, the levels of ATP, ADP, and starch increased significantly. In contrast, both cold shock and wounding of the stigma caused a spontaneous decrease of the CO, content in the measuring chamber, as well as reduced metabolite concentrations in the ovary. Since the transport of labeled auxin from the top to the base of the style lasts at least 45 min, the influence of a chemical substance transmitted within 10 min is unlikely. lhus, our results strongly support the view that different, stimulus-dependent electrical signals cause specific responses of the ovarian metabolism.Since the last century, electrical signaling in plants has been examined, and comprehensive reviews have been published by Pickard (1973) and Sibaoka (1966). An integral part of the generation of action potentials is based on changes in ion flux, including the efflux of chloride and potassium (Oda, 1976;Fromm and Spanswick, 1993) and the influx of calcium (Williamson and Ashley, 1982; Kikuyama and Tazawa, 1983;Beilby, 1984;Beilby and MacRobbie, 1984). In recent years, evidence was given that action potentials may regulate a wide variety of physiological responses in plants, including elongation growth (Shiina and Tazawa, 1986), respiration (Dziubinska et al., 1989), water uptake (Davies et al., 1991), phloem unloading (Fromm, 1991), activation of proteinase inhibitor genes (Wildon et al., 1992), and gas exchange (Fromm and Eschrich, 1993).With regard to pollination, two different kinds of bioelectric potential changes have been observed in the style of flowers. First, Sinyukhin and Britikov (1967) measured an action potential in the style of Lilium martagon and Incarvillea grandiflora a few minutes after placing pollen on the stigma ...