K+ content and concentration within the apoplast of mesophyll tissue of pea (Pisum sativum L., cv Argenteum) leaflets were determined using an elution procedure. Following removal of the epidermis, a 1 centimeter (inside diameter) glass cylinder was attached to the exposed mesophyll tissue and filled with 5 millimolar CaCI2 solution (10C). From time-course curves of cumulative K+ diffusion from the tissue, the amount of K+ of extracellular origin was estimated. Apoplastic K+ contents for leaves from plants cultured in nutrient solution containing 2 or 10 millimolar K+ were found to range from 1 to 4.5 micromoles per gram fresh weight, comprising less than 3% of the total K+ content within the lamina tissue. Assuming an apoplastic solution volume of 0.04 to 0.1 milliliters per gram fresh weight and a Donnan cation exchange capacity of 2.63 micromoles per gram fresh weight (experimentally determined), the K+ concentration within apoplastic solution was estimated at 2.4 to 11.8 millimolar. Net movement of Rb+ label from the extracellular compartment within mesophyll tissue into the symplast was demonstrated by pulse-chase experiments. It was concluded that the mesophyll apoplast in pea has a relatively low capacitance as an ion reservoir. Apoplastic K+ content was found to be highly sensitive to changes in xylem solution concentration.The apoplast within leaf tissue constitutes a potentially important pathway for K+ transport between vascular and mesophyll tissues (6,22,23) accumulate extracellulary within the vascular bundles, whereas lower concentrations would exist within the cell wall of mesophyll tissue more distant from the minor veins.The specific role(s) ofthe apoplast as related to K+ transport and accumulation within leaf lamina tissue cannot be fully elucidated without quantitative analysis of extracellular K+ content and concentration (20). Several indirect approaches have been reported for collection of apoplastic sap and estimation of ionic concentrations including analysis of xylem exudates, vacuum perfusion of leaf lamina discs (1), and pressure dehydration of leaves (14). X-ray microanalysis (7, 9, 12) and ion-sensitive microelectrodes have been used to measure directly extracellular ion concentrations ofepidermal guard cells (2) and the extensor and flexor cells within the pulvinus of legume leaves (26). The primary limitation of these procedures is the inability to estimate the ionic content within the apoplastic reservoir of the mesophyll.Apoplastic ion content is a function of the amount of ion bound to fixed, negatively charged sites within the cell wall, the Donnan free space, and that in solution within the cell wall. Although the cation exchange capacity of leaf cell walls has been investigated for a variety of plant species (19, 25), the 'functional' volume of apoplastic solution in situ is more difficult to estimate. The volume within a unit fresh weight of tissue in theory is influenced by the thickness of the cell walls and the mean size of mesophyll cells. In addition, the vo...