Emergence of Spatial Representation in an Actor-Critic Agent with Hippocampus-Inspired Sequence Generator

Sequential firing of hippocampal place cells is often attributed to sequential sensory drive along a trajectory, and has also been attributed to planning and other cognitive functions. Here, we propose a mechanistic and parsimonious interpretation to complement these ideas: hippocampal sequences arise from intrinsic recurrent circuitry that propagates transient input over long horizons, acting as a temporal memory buffer that is especially useful when reliable sensory evidence is sparse. We implement this idea with a minimal sequence generator inspired by neurobiology and pair it with an actor–critic learner for egocentric visual navigation. Our agent reliably solves a continuous maze without explicit geometric cues, with performance depending on the length of the recurrent sequence. Crucially, the model outperforms LSTM cores under sparse input conditions (16 channels, $\sim2.5\%$ activity), but not under dense input, revealing a strong interaction between representational sparsity and memory architecture. Through learning, units develop localized place fields, distance-dependent spatial kernels, and task-dependent remapping, while inputs to the sequence generator orthogonalize and spatial information increases across layers. These phenomena align with neurobiological data and are causal to performance. Together, our results show that sparse input synergizes with sequence-generating dynamics, providing both a mechanistic account of place cell sequences in the mammalian hippocampus and a simple inductive bias for reinforcement learning based on sparse egocentric inputs in navigation tasks.