The mechanism whereby light generates an electrical signal in photoreceptors has been extensively studied in the intact retina. The uniform organization of the vertebrate photoreceptor layer has aided in the detection of an ionic current that flows extracellularly from the inner segment toward the outer segment of the photoreceptor during darkness (1). Ion substitution experiments indicate that this current is carried by sodium ions which, in the dark, enter the outer segment and maintain the photoreceptor in a depolarized state (2-4). Light stimulation interrupts this current and hyperpolarizes the photoreceptor's membrane (1, 5, 6). Intracellular recording indicates that the cessation of this current is accompanied by a conductance decrease in at least some preparations (7,8). It seems, therefore, that an effect of light on photoreceptors is to decrease a sodium conductance that is high when the photoreceptor is in the dark.The light response, however, is not shaped solely by the light-sensitive conductance changes; intracellular recordings from photoreceptors have shown that the amplitude of the response can be increased when the size of the illuminating spot is increased, even though the irradiance is kept constant (9, 10). Concomitantly, the time course of the response is altered. These changes have been attributed to interactions between photoreceptors (9-11), to voltage-dependent membrane conductances (10, 11), and, for cone photoreceptors, to feedback from second-order neurons (9). Electrical synapses have been proposed to mediate the interaction between photoreceptors (11-15). This notion is supported by experiments showing that cobalt ions, which are assumed to block chemical synaptic transmission, have no detectable effect on the interaction between rod photoreceptors (13). Also, gap junctions (15-17), but not chemical synapses, have been described between photoreceptors in several species. Thus photoreceptors in the intact vertebrate retina form a syncytium. Consequently, current can