It was investigated whether the methyl-erythritol phosphate (MEP) pathway that generates volatile isoprenoids and carotenoids also produces foliar abscisic acid (ABA) and controls stomatal opening. When the MEP pathway was blocked by fosmidomycin and volatile isoprenoid emission was largely suppressed, leaf ABA content decreased to about 50% and leaf stomatal conductance increased significantly. No effect of fosmidomycin was seen in leaves with constitutively high rates of stomatal conductance and in plant species with low foliar ABA concentration. In all other cases, isoprene emission was directly associated with foliar ABA, but ABA reduction upon MEP pathway inhibition was also observed in plant species that do not emit isoprenoids. Stomatal closure causing a midday depression of photosynthesis was also associated with a concurrent increase of isoprene emission and ABA content. It is suggested that the MEP pathway generates a labile pool of ABA that responds rapidly to environmental changes. This pool also regulates stomatal conductance, possibly when coping with frequent changes of water availability. MEP pathway inhibition by leaf darkening, and its down-regulation by exposure to elevated CO 2 , was also associated with a reduction of foliar ABA content. However, stomatal conductance was reduced, indicating that stomatal aperture is not regulated by the MEP-dependent foliar ABA pool, under these specific cases.Volatile isoprenoids (isoprene and monoterpenes) are formed via a chloroplastic pathway (the methylerythritol phosphate [MEP] pathway; Lichtenthaler et al., 1997), predominantly by carbon shunted from the carbon fixation cycle, as indicated by the rapid and quasicomplete labeling of isoprene carbon atoms by 13 C (Delwiche and Sharkey, 1993). The MEP pathway also generates more complex isoprenoids such as carotenoids, essential for chloroplast functioning. Xanthophylls, specialized carotenoids regulating excess energy through the well-described deepoxidation/ epoxidation cycle (Demmig-Adams and Adams, 1996), also act as precursors of abscisic acid (ABA) through the intermediate xanthoxin (Milborrow, 2001;Schwartz et al., 2003). However, multiple ABA pools are present in plants, which may have different biosynthetic and regulatory steps. In leaves, ABA may be also produced after stress episodes, from a pool that is not blocked from carotenoid inhibitors (Li and Walton, 1987). ABA may also accumulate in roots (Cornish and Zeevaart, 1985) and be transported to leaves through the xylem, where it plays an important role in modulating stomatal responses to water stress (Tardieu et al., 1992). ABA has a general role in stress protection, inducing stomatal closure (Mittelheuser and van Steveninck, 1969) and reduction of leaf expansion rate (Zhang and Davies, 1990) under water stress, as well as under several other stress conditions (Milborrow, 2001).Understanding the regulation of ABA biosynthesis and catabolism is key to developing an integrated perspective on plant stress and to linking processes acting at th...