Pattern formation in active biological matter typically arises from the feedback between chemical concentration fields and mechanical stresses. The actomyosin cortex of cells is an archetypal example of an active thin film that displays such patterns. Here, we show how pulsatory patterns emerge in a minimal model of the actomyosin cortex with a single stress-regulating chemical species that exchanges material with the cytoplasm via a linear turnover reaction. Deriving a low-dimensional amplitude-phase model, valid for a one-dimensional periodic domain and a spherical surface, we show that nonlinear waves arise from a secondary parity-breaking bifurcation that originates from the nonreciprocal interaction between spatial modes of the concentration field. Numerical analysis confirms these analytical predictions, and also reveals analogous pulsatory patterns on impermeable domains. Our study provides a generic route to the emergence of nonreciprocity-driven pulsatory patterns that can be controlled by both the strength of activity and the turnover rate.
Picardo et al. (Wed,) studied this question.