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Symmetry-breaking in coupled, identical, fast–slow systems produces a rich, dramatic variety of dynamical behavior—such as amplitudes and frequencies differing by an order of magnitude or more and qualitatively different rhythms between oscillators, corresponding to different functional states. We present a novel method for analyzing these systems. It identifies the key geometric structures responsible for this new symmetry-breaking, and it shows that many different types of symmetry-breaking rhythms arise robustly. We find symmetry-breaking rhythms in which one oscillator exhibits small-amplitude oscillations, while the other exhibits phase-shifted small-amplitude oscillations, large-amplitude oscillations, mixed-mode oscillations, or even undergoes an explosion of limit cycle canards. Two prototypical fast–slow systems illustrate the method: the van der Pol equation that describes electrical circuits and the Lengyel–Epstein model of chemical oscillators. 

Abstract Abrupt (i. e. step) environmental changes, such as natural disasters or the intervention of predators, can alter the internal dynamics of groups with active units, leading to the rapid destruction and/or restructuring of the group, with the emergence of new collective structures that endow the system with adaptability. Few studies, to date, have considered the influence of abrupt environmental changes on emergent behavior. Here, we use a model of active matter, the Belousov‐Zhabotinsky (BZ) self‐oscillating gel, to study the mechanism of formation and transition between modes of collective locomotion caused by changes of illumination intensity in arrays of interacting photosensitive active units. New forms of collective motion can be generated by step changes of illumination intensity. These transformations arise from the phase resetting and wave‐signal regeneration induced by the abrupt parameter variation, while gradual change results in different evolution of collective motion. Our results not only suggest a novel mechanism for emergence, but also imply that new collective behaviors could be accessible via discontinuous parameter changes. 

Abstract Many drugs adjust and/or control the spatiotemporal dynamics of periodic processes such as heartbeat, neuronal signaling and metabolism, often by interacting with proteins or oligopeptides. Here we use a quasi‐biocompatible, non‐equilibrium pH oscillatory system as a biomimetic biological clock to study the effect of pH‐responsive peptides on rhythm dynamics. The added peptides generate feedback that can lengthen or shorten the oscillatory period during which the peptides alternate between random coil and coiled‐coil conformations. This modulation of a chemical clock supports the notion that short peptide reagents may have utility as drugs to regulate human body clocks.