| Abstract: | In controlled-environment studies with debudded Xanthium plants,appreciable changes in stomatal activity and attendant ratesof transpiration were found to be associated with photoperiodicinduction. Leaves of plants kept on a 10-h inductive photoperiodafter removal of the apical and axillary buds grew at ratescomparable to those of similarly debudded plants kept on a 10-h-interruptednon-inductive photoperiod (consisting of an 8-h photoperiodand a 2-h interruption of the dark period). There was a large effect of leaf age on stomatal behaviour:the minimum stomatal resistance of leaves of non-induced plantsdecreased from about 5 s cm–1 when the leaf was 25 percent of its final size to 1.6 s cm–1 when almost fullyexpanded. Thereafter, it slowly increased with time. Superimposedon this age response was a marked effect of photoperiodic induction.The stomata on induced leaves opened more widely than thoseon non-induced leaves, the response being greatest with theleaves which were youngest at the time induction commenced.However, this ‘opening’ tendency was maintainedfor only a few weeks; thereafter, the stomata failed to openas widely. This later ‘closing’ tendency of stomataon leaves of induced plants progressed rapidly and in a basipetalsequence and presaged a necrotic form of leaf senescence whichdeveloped in the same sequence. The closing tendency on leavesof non-induced plants progressed slowly in an acropetal direction;leaves senesced in the same sequence with the familiar yellowingsymptoms. It is suggested that flower induction sets in train a sequenceof events which influence stomatal movement (and other processes)and inevitably leads to the death of the induced axis. Transpiration rates calculated from measurements of the physicalenvironments and stomatal resistances agreed well with thosemeasured. |
