Exposure of the source leaf of bean (Phaseols vulgaris L. cv. Black Valentine) for 2 hours to 2.9 microliters per liter SO2 inhibited the net photosynthetic rate an average of 75% and, simultaneously, the translocation rate an average of45%. Calculations indicated that the experimentally determined translocation rates from S02-stressed leaves were lower than were the rates expected on the basis of the observed reductions in photosynthesis. It is inferred that, under SO2 stress, the phloem-loading system becomes a major lmiting step in controlling the translocation rate.Following removal of SO2, photosynthesis recovered quite rapidly (to about 60% of its preexposure rate within 2 hours), but the translocation rate failed to increase during this time interval. This delayed response of transloation to removal of SO2 does not appear to be due to an injury effect of SO2, inasmuch as a similar effect was obtained by exposing the source leaf to a short (2-hour) interval of dark.Considerable information is now available on the effects of SO2 on photosynthesis in relation to concentration, RH, species, chloroplast physiology, and other factors (see reviews by Heath [8] and Ziegler [17]). Much less is known, however, of its effects on phloem translocation. This paper reports short-term studies on the inhibition and recovery kinetics of phloem translocation in bean plants in response to SO2 exposure of the source leaf.Data presented below suggest that the observed reduction in translocation is actually greater than that which can be expected from the observed reduction in photosynthesis when the source leaf is S02-stressed. We suggest that, under conditions of SO2 exposure, the carrier molecules involved in loading are also damaged, and the loading mechanism thus becomes an important limiting step controlling translocation.The possible involvement of carrier proteins at the sucroseloading sites on the sieve tube-companion cell plasma membranes has been demonstrated by Giaquinta (6, 7), Geiger (4), and others. In particular, it has been shown that relatively nonpermeant sulfhiydryl-specific inhibitors, such asp-chloromercuribenzene sulfonic acid, strongly inhibit loading without affecting photosynthesis (6), indicating that inhibitors are accessible to the carrier molecules via the apoplast. Thus, SO2 or its derivative species, mostly so32 or HS03 in aqueous solution (17), should also have ready access to the carrier proteins. Recently, Noyes (11) reported significant damage to the phloem-loading system in bean by SO2, as inferred from autoradiograms and a reduced efflux rate of pulse-labeled photosynthates.