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Numerous natural systems depend on the sedimentation of passive particles in the presence of swimming microorganisms. Here, we investigate the dynamics of the sedimentation of spherical colloids at various E. coli concentrations within the dilute regime. Results show the appearance of two sedimentation fronts: a spherical particle front and the bacteria front. We find that the bacteria front behave diffusive at short times, whereas at long times it decays linearly. The sedimentation speed of passive particles decays at a constant speed and decreases as bacteria concentration (ϕb) is increased. As ϕb is increased further, the sedimentation speed becomes independent of ϕb. The timescales of the bacteria front are associated with the particle settling speeds. Remarkably, all experiments collapse onto a single master line by using the bacteria front timescale. A phenomenological model is proposed that captures the sedimentation of passive particles in active fluids. 

When stressed sufficiently, solid materials yield and deform plastically via reorganization of microscopic constituents. Indeed, it is possible to alter the microstructure of materials by judicious application of stress, an empirical process utilized in practice to enhance the mechanical properties of metals. Understanding the interdependence of plastic flow and microscopic structure in these nonequilibrium states, however, remains a major challenge. Here, we experimentally investigate this relationship, between the relaxation dynamics and microscopic structure of disordered colloidal solids during plastic deformation. We apply oscillatory shear to solid colloidal monolayers and study their particle trajectories as a function of shear rate in the plastic regime. Under these circumstances, the strain rate, the relaxation rate associated with plastic flow, and the sample microscopic structure oscillate together, but with different phases. Interestingly, the experiments reveal that the relaxation rate associated with plastic flow at time t is correlated with the strain rate and sample microscopic structure measured at earlier and later times, respectively. The relaxation rate, in this nonstationary condition, exhibits power-law, shear-thinning behavior and scales exponentially with sample excess entropy. Thus, measurement of sample static structure (excess entropy) provides insight about both strain rate and constituent rearrangement dynamics in the sample at earlier times.