The role of ethylene (ET) signaling in the responses of two hybrid aspen (Populus tremula L. ϫ P. tremuloides Michx.) clones to chronic ozone (O 3 ; 75 nL L Ϫ1 ) was investigated. The hormonal responses differed between the clones; the O 3 -sensitive clone 51 had higher ET evolution than the tolerant clone 200 during the exposure, whereas the free salicylic acid concentration in clone 200 was higher than in clone 51. The cellular redox status, measured as glutathione redox balance, did not differ between the clones suggesting that the O 3 lesions were not a result of deficient antioxidative capacity. The buildup of salicylic acid during chronic O 3 exposure might have prevented the up-regulation of ET biosynthesis in clone 200. Blocking of ET perception with 1-methylcyclopropene protected both clones from the decrease in net photosynthesis during chronic exposure to O 3 . After a pretreatment with low O 3 for 9 d, an acute 1.5-fold O 3 elevation caused necrosis in the O 3 -sensitive clone 51, which increased substantially when ET perception was blocked. The results suggest that in hybrid aspen, ET signaling had a dual role depending on the severity of the stress. ET accelerated leaf senescence under low O 3 , but under acute O 3 elevation, ET signaling seemed to be required for protection from necrotic cell death.The gaseous phytohormone ethylene (ET) is a signal molecule that is active during both plant development and senescence and is synthesized as a response to several biotic and abiotic stresses (Tingey et al., 1976;Yang and Hoffman, 1984; Abeles et al., 1992;Johnson and Ecker, 1998). The ET precursor 1-aminocyclopropane-1-carboxylic acid (ACC) is synthesized from S-adenosyl-l-Met by ACC synthase (ACS; Yang and Hoffman, 1984). ACC is further converted to CO 2 , cyanide (HCN), and ET by ACC oxidase. The HCN formed is rapidly detoxified by -cyano-Ala synthase (-CAS; Yip and Yang, 1988). ET has a role in the regulation of several plant defense genes (Broglie et al., 1986;Ecker and Davis, 1987;Eyal et al., 1993;Leubner-Metzger et al., 1998), but it also has an opposite role; ET can promote cell death under oxidative stress (Overmyer et al., 2000) and pathogen attack (Ciardi et al., 2001).Tropospheric ozone (O 3 ) has been recognized as a severe air pollutant since the 1950s. Ambient O 3 concentrations in northern Europe vary usually between 20 to 50 nL L Ϫ1 during the growth season, but acute O 3 peaks exceeding 150 nL L Ϫ1 are also regularly observed. Once O 3 enters the leaf through stomata, it degrades rapidly in the apoplast to form various reactive oxygen species (ROS;Mehlhorn et al., 1990;Kanofsky and Sima, 1995;Langebartels et al., 2002). It has been proposed that this apoplastic ROS formation may alter the integrity of the plasma membrane and thus cause cellular damage (Laisk et al., 1989;Heath and Taylor, 1997). To remove and detoxify excess ROS, plants have both enzymatic and nonenzymatic antioxidant defenses such as ascorbic acid, glutathione, ␣-tocopherol, and catalase (Noctor and Foyer, 1998;V...