The existence, characteristics, and behavior of conspecifics are important features of most animals' worlds. Although many animals live in relative isolation, many others interact with members of their own species in critically important ways. Given the importance of social interaction, one would expect that the behavior of others serves as the content of many memories and that such social memories would be an important part of our investigations of animal memory. Although there is increasing evidence that learning from other individuals is important for many animals (e.g., Galef & Laland, 2005;Zentall & Galef, 1988), very little is known about the existence, p properties, or mechanisms of memory for the behavior of other animals.It is well known that the efficiency of choices made by rats in the radial-arm maze task is increased by memories of the spatial locations that they have already chosen and depleted of food (e.g., Olton, 1978;Olton & Samuelson, 1976). Recently, work in our laboratory has shown that rats foraging together with their cagemate in a radial-arm maze are also affected by the choices of the other rat and that at least some of these effects are produced by memory for the choices made earlier during the trial by the other rat (Brown, Farley, & Lorek, 2007;Brown et al., 2008). The nature of the effect produced by choices of the other rat is sometimes an increase in the tendency to visit the locations chosen by it and sometimes an opposite tendency to avoid visits to those locations.Brown et al. (2007) used a free-choice procedure in which two rats chose simultaneously from the eight locations in the maze, as well as an observer/model procedure in which a subject rat observed a model rat make choices in the maze and later made choices itself. In the latter procedure, the subject rat avoided locations that had been chosen by the model rat. In the free-choice procedure, the results were more complicated. There was a tendency to selectively choose the location that had been most recently d visited by the other rat but an opposite tendency to avoid locations visited earlier during the trial by the other rat. Brown et al. (2007) suggested that the physical presence d of the other rat on or near the maze location that it had most recently visited functioned as an attractant stimulus. However, rats avoided locations that they remembered to have been visited earlier during the trial by the other rat.More recently, Brown et f al. (2008) reported a series of experiments using the same free-choice procedure used in some of the experiments reported by Brown et al. (2007). Rather than the usual technique of baiting each maze arm with a small amount of food that is depleted when a rat visits the arm, each maze arm was baited with a large number of pellets, so that food remained throughout each trial. Furthermore, the hedonic value of the food was mad nipulated by baiting some locations with less-preferred grain pellets and other locations with more-preferred sucrose pellets. With one important exception, there ...