Search bioRxivSearch

bioRxiv · 10.1101/521567

The emergence of integrated information, complexity, andconsciousness at criticality

Abstract

Using the critical Ising model of the brain, integrated information as a measure of consciousness is measured in toy models of generic neural networks. Monte Carlo simulations are run on 159 random weighted networks analogous to small 5-node neural network motifs. The integrated information generated by this sample of small Ising models is measured across the model parameter space. It is observed that integrated information, as a type of order parameter not unlike a concept like magnetism, undergoes a phase transition at the critical point in the model. This critical point is demarcated by the peaks of the generalized susceptibility of integrated information, a point where the consciousness of the system is maximally susceptible to perturbations and on the boundary between an ordered and disordered form. This study adds further evidence to support that the emergence of consciousness coincides with the more universal patterns of self-organized criticality, evolution, the emergence of complexity, and the integration of complex systems.\n\nAuthor summaryUnderstanding consciousness through a scientific and mathematical language is slowly coming into reach and so testing and grounding these emerging ideas onto empirical observations and known systems is a first step to properly framing this ancient problem. This paper in particular explores the Integrated Information Theory of Consciousness framed within the physics of the Ising model to understand how and when consciousness, or integrated information, can arise in simple dynamical systems. The emergence of consciousness is treated like the emergence of other classical macroscopic observables in physics such as magnetism and understood as a dynamical phase of matter. Our findings show that the sensitivity of consciousness in a complex system is maximized when the system is undergoing a phase transition, also known as a critical point. This result, combined with a body of evidence highlighting the privelaged state of critical systems suggests that, like many other complex phenomenon, consciousness may simply follow from/emerge out of the tendency of a system to self-organize to criticality.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Khajehabdollahi, S., Abeyasinghe, P., Owen, A., Soddu, A.. 2019-01-15. The emergence of integrated information, complexity, andconsciousness at criticality. https://doi.org/10.1101/521567

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

The Unreasonable Effectiveness of Cell Types in Describing Neuronal Physiological Features

Single-cell RNA sequencing (scRNA-seq) captures detailed gene expression profiles at scale, while patch-clamp recordings measure intrinsic neuronal electrophysiological properties. Modeling the relations between these two modalities remains a challenge. Here, we compare how well electrophysiological features can be predicted by traditional transcriptomic cell type classification, representations derived from a foundational model (scGPT) pretrained on large-scale scRNA-seq datasets, ion channel-coding genes, and highly variable genes. Using paired transcriptomic and electrophysiological patch-sequencing data from 495 human neurons from neurosurgical tissue, we find that cluster-level cell type representations consistently outperform highly variable gene selection, ion channel gene selection, and context-enriched scGPT embeddings. Notably, performance varies across model architectures and initializations, and the best results are obtained by combining the outputs of separate cell type and scGPT-based models. Together, these findings suggest that traditional discrete cellular classification is highly effective in predicting physiological features. For maximum performance it can be complemented by pretrained transformer models.

neuroscience

A nonlinear inhibition pathway underlying cortical responses to tuned holographic optogenetic perturbations

Optogenetics enables causal manipulation of cortical activity. Perturbation responses can be counterintuitive due to network interactions, making theory essential for predicting them. Existing approaches often rely on linear approximations, which fail for many biologically relevant perturbations. Here we develop a nonlinear theory of responses to holographic perturbations in cell-type-specific recurrent networks with structured connectivity. We fit a nonlinear model to mouse V1 data, which shows cotuned-ensemble suppression: perturbing spatially clustered neurons with similar preferred orientations yields markedly stronger short-range suppression than perturbing untuned ensembles. We show that cotuned-ensemble suppression arises from a feature-tuned, nonlinear inhibition pathway implicating somatostatin-positive (SST) interneurons. The theory predicts that cotuned ensembles suppress parvalbumin-positive (PV) neurons but facilitate SST neurons, and links the degree of cotuned-ensemble suppression or facilitation to the variance of the SST response. This framework identifies mechanisms by which nonlinear inhibition sculpts cortical dynamics and establishes a predictive basis for targeted optogenetic interventions.

neuroscience

Proteomic signatures of APOE ε4 across human tissues and cell types in Alzheimers disease

The apolipoprotein E {varepsilon}4 (APOE {varepsilon}4) allele is the strongest genetic risk factor for late-onset Alzheimers disease (AD). However, the underlying molecular mechanisms remain unclear. This study included 1691 participants from the Religious Orders Study and Rush Memory and Aging Project (ROSMAP), 1226 participants from the Accelerating Medicines Partnership - Alzheimers Disease (AMP-AD) Diverse Cohorts Study, and 735 participants from the Alzheimers Disease Neuroimaging Initiative (ADNI). To characterise APOE {varepsilon}4 molecular effects, we analysed proteomic data from plasma, cerebrospinal fluid (CSF), and induced pluripotent stem cell (iPSC)-derived astrocytes and neurons, as well as transcriptomic and proteomic data from multiple brain regions. The association of APOE {varepsilon}4 with AD neuropathology was also examined. APOE {varepsilon}4 carriers shared a plasma proteomic signature enriched for immune processes, irrespective of AD diagnosis. A machine learning classifier trained on this signature discriminated APOE {varepsilon}4 carriers from non-carriers in an independent cohort using CSF proteomics. APOE {varepsilon}4 carriage was associated with higher Braak stages and Consortium to Establish a Registry for Alzheimers Disease (CERAD) score. However, only limited APOE {varepsilon}4-associated transcriptomic and proteomic changes were observed in bulk brain tissue, with poor cross-layer concordance. Proteomic analyses of iPSC-derived astrocytes and neurons further revealed cell-type-specific APOE {varepsilon}4-associated changes. APOE {varepsilon}4 is associated with a consistent proteomic signature across plasma and CSF. Its molecular effects in the brain differ across cell types, brain regions and molecular layers. These findings support the need for cell-type-resolved multi-omic studies to elucidate how APOE {varepsilon}4 confers AD risk.

neuroscience