Dynamical equivalence between resonant translocation of a polymer chain and diversity-induced resonance
Marco Patriarca, Stefano Scialla, Els Heinsalu, Marius E. Yamakou, Julyan H. E. Cartwright
TL;DR
The paper tackles how heterogeneity promotes collective oscillations in networks of nonlinear oscillators, linking diversity-induced resonance (DIR) to a mechanical analog of a dimer/polymer diffusing on a substrate. It introduces a dimer-diffusion resonance (DDR) mechanism and shows that, for networks with zero-mean bias distributions, the system behaves like a 1D polymer whose monomer ordering mirrors the bias values. An analytical condition emerges: resonance occurs when the effective rest length or bias-to-coupling ratio satisfies a critical relation, e.g., $\bar{a}/c \approx \lambda/2$, which for a bistable quartic potential with $\lambda=2$ yields $a^* \approx 0.5$ (for $N=100$, $c=1$). The findings extend from simple two-oscillator models to networks of quartic and FitzHugh–Nagumo oscillators, offering a general, intuitive framework for synchronization in heterogeneous systems with broad biological and technological relevance.
Abstract
Networks of heterogeneous oscillators are often seen to display collective synchronized oscillations, even when single elements of the network do not oscillate in isolation. It has been found that it is the diversity of the individual elements that drives the phenomenon, possibly leading to the appearance of a resonance in the response. Here we study the way in which heterogeneity acts in producing an oscillatory regime in a network and show that the resonance response is based on the same physics underlying the resonant translocation regime observed in models of polymer diffusion on a substrate potential. Such a mechanical analog provides an alternative viewpoint that is useful to interpret and understand the nature of collective oscillations in heterogeneous networks.
