claim
active
claim:the-muscle-itself-peripheral-biological-tissue-can-learn-and-make-decisions-autonomously-not-just-centralized-control-units-like-the-brainThe 'muscle' itself—peripheral biological tissue—can learn and make decisions autonomously, not just centralized control units like the brain
Theoretical claim that physical learning reveals non-modular information processing; contrasts traditional view of separated control (brain) from controlled elements (muscle)
Source paper
extracted_from(2022) · Menachem Stern · Arvind Murugan
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Communities (3)
community
- Levin-led research showing bioelectric signals encode and control anatomical goal states in living systems.
- Cognition and sentience attributed solely via observable behavior, not neural substrate or species.
- Non-neural and neural tissues exhibit autonomous learning and goal-directed behavior in closed-loop systems, from cultured neurons to bioelectric collectives, challenging centralized brain-centric models of cognition.
Frameworks (1)
framework
- Physical learningsupportsFramework for solving inverse problems in which physical systems autonomously adapt their parameters in response to stimuli through local learning rules, without requiring computational design or explicit cost functions
Related by similarity (8)
cosine ≥ 0.65 · no typed edgeEntities in the same semantic neighborhood but without a typed relation to this one — candidates for new edges or unrecognized duplicates.
- Ongoing test prediction: tissues can associate stimuli with rewards to modify anatomy.
- Conditional claim urging consideration of non-neural tissues for cognition.
- Central hypothesis: sentience is not exclusive to neural systems; other biological substrates may achieve felt states.
- Explains the evolutionary pivot from morphospace to behavioral space.
- Second foundational pillar of TAME; supports basal cognition and rejects brain-centrism.
- Central claim about self-maintenance through radical component replacement.