We study a simple stochastic model of neuronal excitatory and inhibitory interactions. The model is defined on a directed lattice and internodes couplings are modulated by a nonlinear function that mimics the process of synaptic activation. We prove that such a system behaves as a fully tunable amplifier: the endogenous component of noise, stemming from finite size effects, seeds a coherent (exponential) amplification across the chain generating giant oscillations with tunable frequencies, a process that the brain could exploit to enhance, and eventually encode, different signals. On a wider perspective, the characterized amplification process could provide a reliable pacemaking mechanism for biological systems. The device extracts energy from the finite size bath and operates as an out of equilibrium thermal machine, under stationary conditions.
We consider a one-dimensional directional array of diffusively coupled oscillators. They are perturbed by the injection of a small additive noise, typically orders of magnitude smaller than the oscillation amplitude, and the system is studied in a region of the parameters that would yield deterministic synchronization. Non normal directed couplings seed a coherent amplification of the perturbation: this latter manifests as a modulation, transversal to the limit cycle, which gains in potency node after node. If the lattice extends long enough, the initial synchrony gets eventually lost and the system moves toward a non trivial attractor, which can be analytically characterized as an asymptotic splay state. The noise assisted instability, ultimately vehiculated and amplified by the non normal nature of the imposed couplings, eventually destabilizes also this second attractor. This phenomenon yields spatiotemporal patterns, which cannot be anticipated by a conventional linear stability analysis. arXiv:1810.01933v1 [cond-mat.dis-nn]
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