Biologypreprint2026-08-02

QUANTUM TUNNELING TO APEX PREDATOR MIGRATION CASCADE: A Comprehensive Monograph on Micro-to-Macro Physical Coupling in Biological Systems

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Abstract

This manuscript establishes a complete, first-principles derivation of the causal pathway linking a single quantum tunneling event in photosynthetic reaction centers to the synchronized migration of apex predators via multi-scale biological transduction. Beginning with the photoexcitation of bacteriochlorophyll special pair (P) in Rhodobacter sphaeroides reaction centers, we derive the full time-dependent Schrödinger equation for non-adiabatic electron transfer, incorporating explicit spatial coordinates for all nuclear and electronic degrees of freedom. The radical pair spin dynamics are solved via the Liouville–von Neumann equation with anisotropic hyperfine coupling tensors expanded to third order in nuclear spin operators. Proton translocation kinetics are quantified through the Nernst–Planck–Poisson system with explicit boundary conditions at the quinone binding sites, yielding the exact proton motive force (Δp = Δψ − (RT/F)ΔpH) with spatially resolved electric potential (Δψ) and pH gradient (ΔpH) components. ATP synthase catalysis is modeled via the three-site binding change mechanism with explicit rotation-angle-dependent free energy landscapes, coupled to L-type calcium channel gating through solved Poisson–Boltzmann equations for surface charge screening. Neurological propagation is derived from the Hodgkin–Huxley formalism with all four ion channel conductance variables (m, h, n, p) expanded as partial differential equations in spatial coordinate x along unmyelinated axons, including explicit terms for sodium–potassium pump electrogenicity. Organismal-scale plume generation is governed by the advection-diffusion-reaction equation for dimethyl sulfide (DMS) in the benthic boundary layer, with source terms derived from hemolymph GPCR-ligand binding kinetics solved via the Koshland–Némethy–Filmer cooperative binding model. Apex predator migration is initiated through lateral line mechanotransduction, where the Navier–Stokes equations for hydrodynamic pressure fluctuations are solved for cupula displacement, yielding explicit stereocilia tip-link tension as a function of spatial coordinates (x,y,z) and time. Finally, central pattern generator (CPG) coupling is derived as a Kuramoto model with asymmetric coupling matrices and explicit conduction delay terms, demonstrating how conspecific vibrational-pheromone entrainment drives phase-locked migration across populations exceeding 10⁴ individuals. Every equation is expanded to its fundamental coordinate components with no abbreviations, placeholders, or omitted steps.

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View paper (DOI)Open access versionOpenAlexZenodo (CERN European Organization for Nuclear Research)Published 2026-08-02

Authors: Brent Allen Jensen