SUMMARY1. The steady-state fluxes of Na, K and Cl ions have been measured in Necturus gall-bladder epithelium by a technique that involves labelling the cells with tracer ions from the mucosal bath only, whilst the serosa is kept at low specific activity.After removing tracer, the efflux is followed into the serosal bath, revealing two exponential components.2. The time constant of the fast component lies between 0-03 and 0 04 s-l and corresponds to that of the extracellular space. The slow component closely matches the cellular efflux, with constants which lie between 0-14 and 0-46 x 10-2s2l.3. Full unstirred-layer calculations have been performed to determine the specific activities in the mucosal solution, the cell and the corium (subepithelium). These involved measuring the diffusion coefficients of Na and Cl in the isolated corium: they are restricted by factors of 0 17 and 0I11.4. The partial flux equations for this double-membrane system have been solved to obtain the cellular fluxes for all three ions. The results indicate that: (i) the net transcellular Na flux is 190 pmol cm-2 s-1, equivalent to the transepithelial salt flux during fluid secretion; (ii) the net transcellular K flux is effectively zero because this ion recirculates across the serosal membrane; (iii) the net transcellular Cl flux is 27 pmol cm-2 s'l, or 15 % of the net transepithelial salt flux.5. The permeability of the paracellular pathway to Cl is 1-65 x I0O-cm s-1 and the available driving forces will allow a maximum net electrodiffusive Cl transport of 10 % through the shunt pathway.