Shin, S.-H.; Lim, H.-Y.; Lee, S.-M.; Seol, J.-M.; Lee, B.; Lee, C.-H.; Naya, Y.; Lee, J.; Lee, I.

In rodents, hippocampal activity is classically described in terms of position-anchored place cells, whereas nonhuman primate work has emphasized spatial view cells, in which activity depends on the region of space being viewed. This contrast has fueled a longstanding debate over whether primate and rodent spatial codes are biologically distinct. We recorded single units in the hippocampus of macaques as they navigated linear tracks in two visually distinct contexts, intermittently making context-dependent object choices. Using a generalized linear model to dissociate position coding from spatial view coding, we identified three coexisting populations in the macaque hippocampus: Position cells, View cells, and Conjunctive cells encoding both variables. Position cells were prevalent and showed rodent-like properties-localized firing, directional tuning, and contextual remapping-even after accounting for visual sampling, whereas View cells stably encoded allocentric visual space. Population decoding confirmed this dissociation at the ensemble level. Robust position codes thus coexist with, yet remain dissociable from, view codes in the primate hippocampus, suggesting that the apparent scarcity of place-like responses in earlier primate work reflects methodological and task-related differences rather than a fundamental species-level divergence.