Interplay between activity, elasticity, and liquid transport in self-contractile biopolymer gels.

Active gels play an important role in biology and in inspiring biomimetic active materials, due to their ability to change shape, size, and create their own morphology. We study a particular class of active gels, generated by polymerizing actin in the presence of cross-linkers and clusters of myosin as molecular motors, which exhibit large contractions. The relevant mechanics for these highly swollen gels is the result of the interplay between activity and liquid flow: gel activity yields a structural reorganization of the gel network and produces a flow of liquid that eventually exits from the gel boundary. This dynamics inherits lengthscales that are typical of the liquid flow processes. The analyses we present provide insights into the contraction dynamics, and they focus on the effects of the geometry on both gel velocity and fluid flow.

Interplay of different environments in open quantum systems: Breakdown of the additive approximation.

We analyze an open quantum system under the influence of more than one environment: a dephasing bath and a probability-absorbing bath that represents a decay channel, as encountered in many models of quantum networks. In our case, dephasing is modeled by random fluctuations of the site energies, while the absorbing bath is modeled with an external lead attached to the system. We analyze under which conditions the effects of the two baths can enter additively the quantum master equation. When such additivity is legitimate, the reduced master equation corresponds to the evolution generated by an effective non-Hermitian Hamiltonian and a Haken-Strobl dephasing super-operator. We find that the additive decomposition is a good approximation when the strength of dephasing is small compared to the bandwidth of the probability-absorbing bath.