A Unified Phase-native Computational Principle Governs Hippocampal Spike Timing and Neural Coding

Human cognition emerges from coordinated spiking dynamics in distributed neural circuits, where information is encoded via both firing rates and precise spike timing determined by brain rhythms. Inspired by this notion, we propose a brain-inspired learning primitive in which cognition-level neural synchrony emerges through iterative bottom-up and top-down interactions between micro-scale dynamics of spiking neurons and a macro-scale mechanism of oscillatory synchronization. Specifically, we model each parcel (e.g., a cortical region or an image pixel) in the target system as a spiking neuron embedded in a predefined connectivity scaffold. Low-level information is encoded in a spatiotemporal domain, where neurons are selectively grouped and fire spontaneously over time through self-organized dynamics. In the bottom-up route, oscillatory synchronization is formed from past spiking activity accumulated over a finite memory window. Since brain dynamics operate in a regime of partial and transient synchronization rather than global phase locking, we model oscillatory coordination using a time-delayed synchronization formulation, which enables a top-down modulation of heterogeneous neural spiking for a large-scale distributed system. Together, we devise a spiking-by-synchronization neural network (S2-Net) that uses rhythmic timing as a control mechanism for efficient information processing. Promising results have been achieved across a broad range of tasks, including neural activity decoding, energy-efficient signal processing, temporal binding and semantic reasoning.

Artificial neural networks (ANN) provide accurate continuous-valued representation, whereas spiking neural networks (SNN) offer event-driven temporal processing, yet both paradigms face limitations when value encoding and timing dynamics must be learned within a single computational structure. This paper introduces a network based on Unified Complex-valued Neuron (UCN), a new neural computational model that integrates continuous activation and phase-driven event generation through an asymmetric complex-valued state. In the UCN, magnitude encodes signal strength while phase governs intrinsic temporal evolution and valued spike emission. A foundational training framework combining backpropagation (BP) and backpropagation through time (BPTT) is first developed to optimize magnitude and phase pathways in a unified way. To reduce computational complexity, an event-driven adaptive phase learning (EAPL) rule is then introduced as a more efficient alternative. The proposed model is evaluated through object tracking and Lorenz attractor learning. Results demonstrate that UCN-based Network (UCNN) provides accurate, stable, and interpretable spatiotemporal learning while preserving sparse event-driven computation for neuromorphic and edge-AI applications.

Hippocampal place and time cells encode spatial and temporal aspects of experience. Both have the same neural substrate, but have been modeled as having different functions and mechanistic origins, place cells as continuous attractors, and time cells as leaky integrators. Here, we show that both types emerge from two dynamical regimes of a single recurrent network (RNN) modeling hippocampal CA3 as a predictive autoencoder. The network receives simulated, partially occluded experience vectors" containing spatial patterns (location-specific activity sampled during environmental traversal) and/or temporal patterns (correlated activity pairs separated by void" intervals), and is trained to reconstruct missing input. During spatial navigation, the network generates stable attractor-like place fields. But trained on temporally structured inputs, the network produces sequentially broadened fields, recapitulating time cells. By varying spatio-temporal input patterning, we observe hidden units transition smoothly between time cell-like and place cell-like representations. These results suggest a shared origin, but task-driven difference, between place and time cells.