Guardat en:
| Autor principal: | |
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| Format: | Recurso digital |
| Idioma: | anglès |
| Publicat: |
Zenodo
2026
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| Matèries: | |
| Accés en línia: | https://doi.org/10.5281/zenodo.20077420 |
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Taula de continguts:
- <p>This document presents a standalone USP Field Theory interpretation of human senses as biological resonance detectors. Rather than replacing mainstream sensory biology, the framework offers a physical mechanism layer for why sensory systems behave as tuned, damped, thresholded, adaptive detectors.</p> <p>The document covers vision, hearing, smell, taste, touch, temperature, pain, balance, proprioception, and internal sensing. Each sense is interpreted as a receptor interface that converts an external or internal disturbance into a bounded biological response.</p> <p>In this framework, the central quantity is the mismatch parameter Δf, interpreted operationally through photon energy, pressure-wave frequency, molecular vibrational modes, conformational transition energies, hydration-shell rearrangements, membrane deformation, ion-channel gating, and receptor relaxation time.</p> <p>Special emphasis is given to taste and smell. Taste is interpreted as hydrated molecular-surface resonance, where dissolved molecules and ions interact with receptor surfaces through local geometry, hydration structure, charge distribution, and conformational compatibility. Smell is treated as a coupled process involving shape recognition, binding energy, local vibration, and receptor dynamics.</p> <p>The work remains compatibility-first. Phototransduction, cochlear mechanics, olfactory receptors, taste GPCRs, ion channels, mechanotransduction, and neural coding remain the standard predictive layer. USP supplies an interpretive resonance-geometry layer, consistent with the broader molecular-resonance framework where bonding creates collective modes and new effective mismatch boundaries.</p> <p>The document also includes falsifiable experimental pathways using receptor-level spectroscopy, impedance measurements, hydration-damping tests, isotopologue comparisons, organoids, membrane patches, electrophysiology, and controlled psychophysics datasets. It includes non-circular calibration rules, predeclared thresholds, statistical null models, and safety guardrails.</p>