Accumulation of Cs' by Chlovelfa salina was 28-fold greater in cells incubated in the presence than in the absence of 0.5 M-NaCl. An approximate 70% removal of external Cs+ resulted after 15 h incubation of cells with 50 ~L MCsCl and 0.5 M-NaCI. LiCl also had a stimulatory effect on Cs' uptake, although manaitol did not. Cs+ influx increased with increasing external NaCl concentration and was maximal between 25-500 mM-NaC1 at approximately 4 nmol Cs+ h-' (lo6 cells)-'. Little effect on Cs+ uptake resulted from the presence of Mg2+ or Cat+ or from varying the external pH, and Cs' was relatively non-toxic towards C. safina. At increasing cell densities (from 4 x lo5 to 1 x 10' cells ml-'), decreasing amounts of Cs+ were accumulated per cell although the rate of Cs+ removal from the external medium was still greatest at the higher cell densities examined. Freely suspended C. salina and cell-loaded alginate microbeads accumulated similar levels of CS+, however, 46% of total Cs' uptake was attributable to the calcium-alginate matrix in the latter case. When Cs+-loaded cells were subjected to hypoosmotic shock, loss of cellular Cs' occurred allowing easy Cs' recovery. This loss exceeded 90% of cellular Cs' when cells were washed with solutions containing < 50 mM-NaC1 between consecutive Cs' uptake periods; these cells subsequently lost their ability to accumulate large amounts of Cs+. Maximal Cs + uptake (approximately 85-1 YO removal after three 15 h incubations) occurred when cells were washed with a solution containing 500 m~-NaCl and 200 rnM-KC1 between incubations. The relevance of these results to the possible use of C. salinu in a saltdependent biological Cs-removal process is discussed.