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Historical Constraints on Neural State Space: Measuring Assembly Depth via Eigenvalue Distribution Structure

Kimiyasu Igarashi

Zenodo (CERN European Organization for Nuclear Research) May 31, 2026 DOI: 10.5281/zenodo.20415592 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Simulation study Peer reviewed
Keywords Multiplicative function Consciousness Attractor Cognition Exaptation Bounded function Perception Topology electrical circuits Artificial intelligence Cognitive science Premise Theoretical computer science
Key points History-dependent (biological) gain actively low-dimensionalizes neural state space in a manner robust to input diversity, while fixed (AI-style) gain passively reflects input diversity as high-dimensional spread.

Abstract

A central unresolved question in computational consciousness research concerns whether meaningful differences between biological and artificial systems can be quantified without recourse to computationally intractable measures such as Integrated Information Theory (IIT). We propose Participation Ratio (PR) — derived from the eigenvalue distribution of neural trajectory covariance matrices — as a tractable proxy for the effective dimensionality of state-space usage. We show through simulation that history-dependent (biological) gain formation and fixed (AI-style) gain produce qualitatively distinct PR signatures: biological gain actively low-dimensionalizes the state space in a manner robust to input diversity, while AI fixed gain passively reflects input diversity as high-dimensional spread. This active low-dimensionalization is interpreted via the Maximum Entropy principle (Savin & Tkacik, 2017): history-dependent gain formation imposes structured constraints on eigenvalue distributions, converging toward a low-PR attractor state regardless of environmental variability. The result connects to Shine et al. (2018) on gain-mediated segregation/integration transitions, Claudi et al. (2025) MADE framework for attractor manifold topology, and Ferguson & Cardin (2020) on cortical gain modulation mechanisms. We propose PR as a practically computable, neurobiologically grounded index for comparing the structural organization of biological and artificial information processing