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Critical Scaling and Metabolic Regulation in a Ginzburg--Landau Theory of Cognitive Dynamics

24 February 2026 at 13:00
arXiv:2602.19023v1 Announce Type: cross Abstract: We formulate a phenomenological effective field theory in which biological intelligence emerges as a macroscopic order parameter sustained by continuous metabolic flux. By modeling cognition as a coarse-grained neural activity field governed by a variational free energy, we derive closed-form expressions for information capacity and structural susceptibility using a Gaussian maximum entropy approximation. The theory predicts a universal algebraic divergence of the susceptibility, $\chi \sim K^{-3/2}$, as the structural stiffness $K$ approaches the instability threshold. The exponent $\gamma = 3/2$ is consistent with the mean-field branching process universality class, thereby providing a theoretical rationale for the observed avalanche size exponent $\tau \approx 3/2$ in cortical dynamics without invoking microscopic equivalence. We identify adult cognition as a metabolically pinned non-equilibrium steady state maintained near the critical regime $\Gamma \equiv K/\alpha \approx 1$ by continuous metabolic regulation, while pathological decline corresponds to a delocalization transition triggered by the violation of structural stability conditions. The framework generates concrete, falsifiable predictions for attention scaling, altered states of consciousness, and transcranial magnetic stimulation responses, each of which can be tested against existing neuroimaging and electrophysiological datasets.

AI-driven Large-scale Electron Microscopy enables Whole-tissue Subcellular Digitization

By: Li Xiao Β· Liqing Liu Β· Hongjun Wu Β· Jiayi Zhong Β· Xixia Li Β· Yan Zhang Β· Junjie Hu Β· Sun Fei Β· Ge Yang Β· Tao Xu
24 February 2026 at 13:00
arXiv:2511.02860v2 Announce Type: replace-cross Abstract: The distribution and interactions of cellular organelles play a critical role in mediating cellular physiology and pathology. Large-scale electron microscopy enables visualization of organelle distribution and interactions at the tissue level with nanometer resolution, but robust and efficient computational analysis tools are lacking. Here, we present a deep learning tool for universal large-scale 2D/3D electron microscopy analysis, DeepOrganelle. This new tool enables high-throughput, cell-resolved spatiotemporal mapping and digitization of organelle distribution and interactions. When applied to spermatogenesis across 12 stages and 22 differentiation status of the germ cells, DeepOrganelle uncovered previously unrecognized, stage-dependent dynamics of mitochondria-endoplasmic reticulum contact sites within one subphase of prophase I during meiosis. It also revealed coordinated organelle redistribution in Sertoli cells towards the blood-testis barrier, digitizing the remodeling dynamics of the tissue. This study demonstrates that DeepOrganelle provides a powerful framework that captures subcellular dynamics at the whole-tissue level.

Coevolutionary balance of resting-state brain networks in autism

arXiv:2507.09045v3 Announce Type: replace Abstract: Autism spectrum disorder (ASD) is associated with atypical large-scale brain organization, yet the functional principles underlying these alterations remain incompletely understood. We examined whether coevolutionary balance, a network-level energy measure derived from signed interactions and nodal activity states, captures disruptions in resting-state functional connectivity in autistic adults. Using resting-state fMRI data from ABIDE I with ComBat harmonization to mitigate multi-site batch effects, we constructed whole-brain networks by combining binarized fALFF activity with signed functional correlations and quantified their coevolutionary energy. In the primary analysis with global signal regression (GSR), the ASD group showed significantly more negative global coevolutionary energy (pFDR
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