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Chemical concentration fields and flow patterns inside and outside of a spherical active droplet powered by collective chemotaxis. 

The phenomenon of the ‘coil-stretch’ (C-S) transition, wherein a long-chain polymer initially in a coiled state undergoes a sudden configuration change to become fully stretched under steady elongational flows, has been widely recognized. This transition can display intricate hysteresis behaviours under specific critical conditions, giving rise to unique rheological characteristics in dilute polymer solutions. Historically, microscopic stochastic models and Brownian dynamics simulations have shed light on the underlying mechanisms of the transition by uncovering bistable configurations of polymer chains. Following the initial work by Cerf (J. Chem. Phys., vol. 20, 1952, pp. 395–402), we introduce a continuum model in this study to investigate the C-S transition in a constant uniaxial elongational flow. Our approach involves approximating the unfolding process of the polymer chain as an axisymmetric deformation of an elastic particle. We make the assumption that the particle possesses uniform material properties, which can be represented by a nonlinear, strain-hardening constitutive equation to replicate the finite extensibility of the polymer chain. Subsequently, we analytically solve for the steady-state deformation using a polarization method. By employing this reduced model, we effectively capture the C-S transition and establish its specific correlations with material and geometric properties. The hysteresis phenomena can be comprehended through a force-balance analysis, which involves comparing the externally applied viscous forces with the intrinsic elastic responsive forces. We demonstrate that our model, while simple, unveils rich elastohydrodynamics of the C-S transition. 

Dense assemblies of self-propelling rods (SPRs) may exhibit fascinating collective behaviors and anomalous physical properties that are far away from equilibrium. Using large-scale Brownian dynamics simulations, we investigate the dynamics of disclination defects in 2D fluidized swarming motions of dense dry SPRs ( i.e. , without hydrodynamic effects) that form notable local positional topological structures that are reminiscent of smectic order. We find the deformations of smectic-like rod layers can create unique polar structures that lead to slow translations and rotations of ±1/2-order defects, which are fundamentally different from the fast streaming defect motions observed in wet active matter. We measure and characterize the statistical properties of topological defects and reveal their connections with the coherent structures. Furthermore, we construct a bottom-up active-liquid-crystal model to analyze the instability of polar lanes, which effectively leads to defect formation between interlocked polar lanes and serves as the origin of the large-scale swarming motions. 

Microorganisms can efficiently navigate in anisotropic complex fluids, but the precise swimming mechanisms remain largely unexplored. Their dynamics are determined by the interplay between multiple effects, including the fluid's orientation order, swimmer's undulatory gait, and the finite length. Here we extend the numerical study of the two-dimensional undulatory motions of a flexible swimmer in lyotropic liquid-crystalline polymers (LCPs) by Lin et al. (2021) to the scenarios of arbitrary swimming directions with respect to the nematic director. The swimmer is modeled as a nearly inextensible yet flexible fiber with imposed traveling-wave like actuation. We investigate the orientation-dependent swimming behaviors in nematic LCPs for an infinite long sheet (i.e., Taylor's swimming sheet model) and finite-length swimmers. We demonstrate that the swimmer must be sufficiently stiff to produce undulatory deformations to gain net motions. Moreover, a motile finite-length swimmer can reorient itself to swim parallel with the nematic director, due to a net body torque arising from the asymmetric distribution of the polymer force along the body. 

Microorganisms may exhibit rich swimming behaviours in anisotropic fluids, such as liquid crystals, which have direction-dependent physical and rheological properties. Here we construct a two-dimensional computation model to study the undulatory swimming mechanisms of microswimmers in a solution of rigid, rodlike liquid crystal polymers. We describe the fluid phase using Doi's $$Q$$ -tensor model, and treat the swimmer as a finite-length flexible fibre with imposed propagating travelling waves on the body curvature. The fluid–structure interactions are resolved via an immersed boundary method. Compared with the swimming dynamics in Newtonian fluids, we observe non-Newtonian behaviours that feature both enhanced and retarded swimming motions in lyotropic liquid crystal polymers. We reveal the propulsion mechanism by analysing the near-body flow fields and polymeric force distributions, together with asymptotic analysis for an idealized model of Taylor's swimming sheet.