Synchronization plays a crucial role in the dynamics of living organisms. Uncovering the mechanism behind it requires an understanding of individual biological oscillators and the coupling forces between them. Here, a single-cell assay is developed that studies rhythmic behavior in the motility of E. coli cells that can be mutually synchronized. Circular microcavities are used to isolate E. coli cells that swim along the cavity wall, resulting in self-sustained oscillations. Connecting these cavities by microchannels yields synchronization patterns with phase slips. It is demonstrated that the coordinated movement observed in coupled E. coli oscillators follows mathematical rules of synchronization which is used to quantify the coupling strength. These findings advance the understanding of motility in confinement, and open up new opportunities for engineering networks of coupled oscillators in microbial active matter.@en

Mechanical sources of nonlinear damping play a central role in modern physics, from solid-state physics to thermodynamics. The microscopic theory of mechanical dissipation suggests that nonlinear damping of a resonant mode can be strongly enhanced when it is coupled to a vibration mode that is close to twice its resonance frequency. To date, no experimental evidence of this enhancement has been realized. In this letter, we experimentally show that nanoresonators driven into parametric-direct internal resonance provide supporting evidence for the microscopic theory of nonlinear dissipation. By regulating the drive level, we tune the parametric resonance of a graphene nanodrum over a range of 40–70 MHz to reach successive two-to-one internal resonances, leading to a nearly two-fold increase of the nonlinear damping. Our study opens up a route towards utilizing modal interactions and parametric resonance to realize resonators with engineered nonlinear dissipation over wide frequency range.

@en