The Belousov-Zhabotinsky reaction reveals two regimes of non-Arrhenius temperature scaling in relaxation oscillators

Abstract

The period of biological and chemical oscillators scales with temperature in a characteristic way. Some oscillators are very well described by an Arrhenius law, while others show systematic deviations. Several frameworks have been proposed to explain such deviations, but they are either phenomenological, focus on activation energy imbalances in specific circuits, or restrict themselves to sequential processes. Here we develop a mechanistic account of the temperature scaling of relaxation oscillators, using the Belousov-Zhabotinsky (BZ) reaction as a model system. We distinguish two typical scenarios by their temperature-scaling signatures. In the first, an Arrhenius-dependent timescale separation parameter produces a biphasic Arrhenius scaling of the period as the oscillator approaches a Hopf bifurcation. In the second, Arrhenius-dependent nullclines hide the same bifurcation behind a canard explosion, yielding apparent single-line Arrhenius scaling. Measuring the electrode potential of a classical and an uncatalyzed BZ reaction, over a very wide temperature range ({\approx} 100 °C), and comparing to dynamical models, we find that the two reactions represent these two distinct scenarios. Furthermore, we show that a single parameter characterizing the waveform asymmetry between fast and slow phases quantitatively predicts the temperature scaling of three other observables close to the Hopf bifurcation: the period, amplitude, and phase noise. This analysis also recovers elementary activation energies of the BZ mechanism, including a new estimate for the autocatalytic step. We discuss how this framework and its waveform-based diagnostics apply to the analysis of general biochemical relaxation oscillators