The precision principle: driving biological self-organization

In this perspective, we introduce the <i>Precision Principle</i> as a unifying theoretical framework to explain self-organization across biological systems. Drawing from neurobiology, systems theory, and computational modeling, we propose that precision, understood as constraint-driven coherence, is the key force shaping the architecture, function, and evolution of nervous systems. We identify three interrelated domains: Structural Precision (efficient, modular wiring), Functional Precision (adaptive, context-sensitive circuit deployment), and Evolutionary Precision (selection-guided architectural refinement). Each domain is grounded in local operations such as spatial and temporal averaging, multiplicative co-activation, and threshold gating, which enable biological systems to achieve robust organization without centralized control. Within this framework, we introduce the <i>Precision Coefficient</i>, <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:mi>P</mml:mi> <mml:mrow> <mml:mfenced><mml:mrow><mml:mi>z</mml:mi></mml:mrow> </mml:mfenced> </mml:mrow> <mml:mo>=</mml:mo> <mml:mi>C</mml:mi> <mml:mrow> <mml:mfenced><mml:mrow><mml:mi>z</mml:mi></mml:mrow> </mml:mfenced> </mml:mrow> <mml:mo>-</mml:mo> <mml:mi>α</mml:mi> <mml:mi>R</mml:mi> <mml:mrow> <mml:mfenced><mml:mrow><mml:mi>z</mml:mi></mml:mrow> </mml:mfenced> </mml:mrow> </mml:mrow> </mml:math> , which formalizes the balance between network coherence and resource cost and serves as a simple quantitative outline of the principle. Conceptually, this formalism aligns with established learning mechanisms: Hebbian reinforcement provides the local substrate for weight changes, while winner-take-all and k-winners competition selectively eliminates weaker synapses, together increasing <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:mi>C</mml:mi> <mml:mrow> <mml:mfenced><mml:mrow><mml:mi>z</mml:mi></mml:mrow> </mml:mfenced> </mml:mrow> </mml:mrow> </mml:math> and reducing redundancy within <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:mi>R</mml:mi> <mml:mrow> <mml:mfenced><mml:mrow><mml:mi>z</mml:mi></mml:mrow> </mml:mfenced> </mml:mrow> </mml:mrow> </mml:math> . Rather than framing the theory in opposition to existing models, we aim to establish the <i>Precision Principle</i> as an original, integrative lens for understanding how systems sustain efficiency, flexibility, and resilience. We hope the framework inspires new research into neural plasticity, development, and artificial systems, by centering internal coherence, not prediction or control, as the primary driver of self-organizing intelligence.

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Publication Details

Journal
Frontiers in Network Physiology
Published
2025-11-12
DOI
https://doi.org/10.3389/fnetp.2025.1678473
Primary Topic
Slime Mold and Myxomycetes Research
Type
article
Field-Weighted Citation Impact
0.00

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article

The precision principle: driving biological self-organization

Amedeo D’Angiulli, Birgitta Dresp, Gabriel Byczynski, Raymond S. Roy et al.
Frontiers in Network Physiology
Slime Mold and Myxomycetes Research
article

The precision principle: driving biological self-organization

Amedeo D’Angiulli, Birgitta Dresp, Gabriel Byczynski, Raymond S. Roy, Kiranpreet Sidhu
article en

Abstract

In this perspective, we introduce the <i>Precision Principle</i> as a unifying theoretical framework to explain self-organization across biological systems. Drawing from neurobiology, systems theory, and computational modeling, we propose that precision, understood as constraint-driven coherence, is the key force shaping the architecture, function, and evolution of nervous systems. We identify three interrelated domains: Structural Precision (efficient, modular wiring), Functional Precision (adaptive, context-sensitive circuit deployment), and Evolutionary Precision (selection-guided architectural refinement). Each domain is grounded in local operations such as spatial and temporal averaging, multiplicative co-activation, and threshold gating, which enable biological systems to achieve robust organization without centralized control. Within this framework, we introduce the <i>Precision Coefficient</i>, <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:mi>P</mml:mi> <mml:mrow> <mml:mfenced><mml:mrow><mml:mi>z</mml:mi></mml:mrow> </mml:mfenced> </mml:mrow> <mml:mo>=</mml:mo> <mml:mi>C</mml:mi> <mml:mrow> <mml:mfenced><mml:mrow><mml:mi>z</mml:mi></mml:mrow> </mml:mfenced> </mml:mrow> <mml:mo>-</mml:mo> <mml:mi>α</mml:mi> <mml:mi>R</mml:mi> <mml:mrow> <mml:mfenced><mml:mrow><mml:mi>z</mml:mi></mml:mrow> </mml:mfenced> </mml:mrow> </mml:mrow> </mml:math> , which formalizes the balance between network coherence and resource cost and serves as a simple quantitative outline of the principle. Conceptually, this formalism aligns with established learning mechanisms: Hebbian reinforcement provides the local substrate for weight changes, while winner-take-all and k-winners competition selectively eliminates weaker synapses, together increasing <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:mi>C</mml:mi> <mml:mrow> <mml:mfenced><mml:mrow><mml:mi>z</mml:mi></mml:mrow> </mml:mfenced> </mml:mrow> </mml:mrow> </mml:math> and reducing redundancy within <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:mi>R</mml:mi> <mml:mrow> <mml:mfenced><mml:mrow><mml:mi>z</mml:mi></mml:mrow> </mml:mfenced> </mml:mrow> </mml:mrow> </mml:math> . Rather than framing the theory in opposition to existing models, we aim to establish the <i>Precision Principle</i> as an original, integrative lens for understanding how systems sustain efficiency, flexibility, and resilience. We hope the framework inspires new research into neural plasticity, development, and artificial systems, by centering internal coherence, not prediction or control, as the primary driver of self-organizing intelligence.

Frontiers in Network PhysiologyVol. 5
Children's Hospital of Eastern Ontario (CA), University Hospital of Geneva (CH), Geneva College (US), Carleton University (CA), Université de Strasbourg (FR)
Universidade de São Paulo
Openalex Percentile: Top 67%
Slime Mold and Myxomycetes Research
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