The electrogenic Na-K pump coupling ratio in the large neurons of the lobster cardiac ganglion was determined by two different electrophysiological techniques . A graphical analysis plotting exp(E.F/RT) vs .[K]o after the pump was blocked by ouabain was used to determine values for [K]i, PNa/PK, and the pump coupling ratio. These measurements were made 4-8 h after the cells were penetrated with microelectrodes, and thus represent non-Na-loaded steady state values . The value obtained for the pump coupling ratio under these conditions was 1 .44 ± 0.06 (11 = 9) or close to 3 Na for 2 K. The second technique used to measure the coupling ratio was to iontophoretically inject Na ions into the neuron . Neurons were penetrated with three microelectrodes, two of which were filled with 2 M Na-citrate ; the third electrode contained either 2 M K-citrate or 3 M KCI. By passing current between the Na salt-containing electrodes, Na was injected into the cell soma . The injection system was calibrated by injecting z4 Na-citrate into counting vials from representative microelectrodes (calculated z4 Na transport = 0.92) . By knowing the Na load injected into the cells, and by measuring the time-current area produced by the Na activation of the Na-K pump, the coupling ratio was calculated to be 1 .54 ± 0.05 ()1 = 19), which is not significantly different from the value obtained by the first method . This value represents a Na-loaded experimental situation . When Na was removed from the external bathing solution, the coupling ratio shifted to 2 Na to 1 K (2 .0 ± 0.07, 11 = 4) . These results suggest that the pump normally operates with a 3 :2 ratio both in steady state and under Na load but that in the absence of external Na, it can operate with less than a full complement (2) of K on the external surface of the pump .