Cotton (Gossypium hirsutum L. cv Acala SJ-2) seedlings were grown in nutrient solutions with four combinations of NaCI (0.1 and 150 millimolar) and CaC12 (1 and 10 millimolar) for 7 days, and then exposed to [14Cjglucose for 5 hours. Uptake and incorporation of j'4Clglucose into various cell wall fractions of the root tips were determined. At 1 millimolar Ca2 , treatment with 150 millimolar NaCl slightly stimulated uptake but considerably inhibited glucose incorporation into noncellulosic and cellulosic polysaccharides. Supplemental Ca2' did not affect incorporation of glucose into the noncellulosic fraction (regardless of NaCl treatment) but completely alleviated the inhibitory effect of NaCI on glucose incorporation into cellulose. We suggest that high Na' concentrations reduce synthesis of cellulose in cotton roots via disturbance of plasma membrane integrity and that supplemental Ca2" counteracts this effect. The effects on cellulose biosynthesis are proposed to be related to Ca2' displacement from the plasma membrane. Salt stress is characterized by an inhibition of growth in many crop plants. This inhibition may be caused by osmotic effects, ion toxicity, ion imbalance or a combination of these factors. Calcium is a particularly important nutrient in plants exposed to NaCl stress because of its role in maintaining the structural and functional integrity of membranes (18,20) MATERIALS AND METHODS Plant Material. Cotton seeds (Gossypium hirsutum L. cv Acala SJ-2) were imbibed in aerated deionized water for 15 h and then planted between strips of germination paper as described previously (14). The strips were rolled to form a 'cigar' and placed into 500-mL glass beakers containing 100 mL 0.5 mM CaSO4. The beakers were covered with plastic wrap to minimize evaporation and salt accumulation on the germination paper, and then placed in a germination cabinet for 48 h in the dark at 27°C. Five germinated seeds with a taproot length of about 5 cm were transferred to small plastic containers with 120 mL of control solution and allowed to grow for 2 d in the growth chamber under low light condition (200-250 ,mol m-2 s-'). The growth temperature was maintained at 26/18°C day/night. Relative humidity varied between 70 and 85%. The control solution was a 1/10 strength modified Hoagland nutrient solution (9) but containing 1 mm Ca2 . On the 3rd d of growing in the control solution, the salinization treatment was initiated with increments of 50 mM NaCl each day up to 150 mm. The three treatment solutions were prepared by adding NaCl and CaCl2 to the control solution to final concentrations of 150 mM NaCl, 10 mM CaCl2, and 150 mm NaCl plus 10 mm CaCl2, respectively. The initial pH of the growth solutions was 5.6. The growth solution was changed every day.