Water-relation parameters of leaf mesophyll cells of the CAM plant Kaklchoi daigremontiana have been determined directly in cells of tissue slices using the pressure-probe technique. Turgor pressures measured in cells of the second to fourth layer from the cut surface showed an average of 1.82 ± 0.62 bar (mean ± SD; n = 157 cells). This was lower than expected from measurements of the osmotic pressure of the cell sap. The half-time (T112) for water-flux equilibration of individual cels was 2.5 to 8.8 seconds. This is the fastest T112 found so far for higher-plant cells. The calculated values of the hydraulic conductivity were in the range of 0.20 to 1.6 x 10-5 centimeters second-' bar-', with an average of (0.69 ± 0.46) x 10-5 centimeters second`bar-' (mean + SD; n = 8 cells). The T1/2 values of water exchange of individual cells are consistent with the overall rates of water-flux equilibration measured for tissue slices.The volumetric elastic moduli (e) of individual cells were in the range 13 to 128 bar for turgor pressures between 0.0 and 3.4 bar, the average e value was 42.4 ± 27.7 bar (mean ± SD; n = 21 cells). This e value is similar to that observed for other higher-plant cells.The of CO2 fixation during the dark period (e.g. refs. 3, 12, 13, 22). However, it is not clear whether the occurrence of CAM is associated with particular water-relation parameters of CAM-performing cells, such as the turgidity of cells, the water permeability of cell membranes and the elastic extensibility of cell walls.The osmotic processes that occur during the CAM rhythm may be rate-limited at different levels, ie. at the level of either solute (malic acid) or water transport, of solute synthesis and degradation, or by the mechanical extensibility of solute-and waterstoring cells (18). Interrelations may occur (8) between waterrelation characteristics of CAM-performing cells and (a) intracellular (tonoplast) transport of malic acid (10, 11), (b) synthesis and degradation of malate in the cytoplasm, and (c) the rhythm of stomatal movement. At the morphological level, CAM seems only to be found in tissues possessing voluminous cells containing chloroplasts and large vacuoles. As a consequence, the plant organs containing these tissues are normally "succulent," but it has proved hard to formulate a satisfactory definition of "succulence" from a physiological and biophysical point of view.For a decision as to whether plant water status plays a key role in the induction and control of CAM, the water-relation parameters2 (i.e. cell P, water-exchange rates (T1/2 values), Lp and e) of individual cells must be known. Such measurements have become possible with the introduction of the pressure-probe technique, which was developed first for giant algal cells (17,19,21,27)