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تسجيل مستخدم جديدTraffic jams, gliders, and bands in the quest for collective motion
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We study a simple swarming model on a two-dimensional lattice where the self-propelled particles exhibit a tendency to align ferromagnetically. Volume exclusion effects are present: particles can only hop to a neighboring node if the node is empty. Here we show that such effects lead to a surprisingly rich variety of self-organized spatial patterns. As particles exhibit an increasingly higher tendency to align to neighbors, they first self-segregate into disordered particle aggregates. Aggregates turn into traffic jams. Traffic jams evolve toward gliders, triangular high density regions that migrate in a well-defined direction. Maximum order is achieved by the formation of elongated high density regions - bands - that transverse the entire system. Numerical evidence suggests that below the percolation density the phase transition associated to orientational order is of first-order, while at full occupancy it is of second-order. The model highlights the (pattern formation) importance of a coupling between local density, orientation, and local speed.
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Collective motion is found in various animal systems, active suspensions and robotic or virtual agents. This is often understood using high level models that directly encode selected empirical features, such as co-alignment and cohesion. Can these fe
atures be shown to emerge from an underlying, low-level principle? We find that they emerge naturally under Future State Maximisation (FSM). Here agents perceive a visual representation of the world around them, such as might be recorded on a simple retina, and then move to maximise the number of different visual environments that they expect to be able to access in the future. Such a control principle may confer evolutionary fitness in an uncertain world by enabling agents to deal with a wide variety of future scenarios. The collective dynamics that spontaneously emerge under FSM resemble animal systems in several qualitative aspects, including cohesion, co-alignment and collision suppression, none of which are explicitly encoded in the model. A multi-layered neural network trained on simulated trajectories is shown to represent a heuristic mimicking FSM. Similar levels of reasoning would seem to be accessible under animal cognition, demonstrating a possible route to the emergence of collective motion in social animals directly from the control principle underlying FSM. Such models may also be good candidates for encoding into possible future realisations of artificial intelligent matter, able to sense light, process information and move.
We characterize cell motion in experiments and show that the transition to collective motion in colonies of gliding bacterial cells confined to a monolayer appears through the organization of cells into larger moving clusters. Collective motion by no
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Locomotion and transport of microorganisms in fluids is an essential aspect of life. Search for food, orientation toward light, spreading of off-spring, and the formation of colonies are only possible due to locomotion. Swimming at the microscale occ
urs at low Reynolds numbers, where fluid friction and viscosity dominates over inertia. Here, evolution achieved propulsion mechanisms, which overcome and even exploit drag. Prominent propulsion mechanisms are rotating helical flagella, exploited by many bacteria, and snake-like or whip-like motion of eukaryotic flagella, utilized by sperm and algae. For artificial microswimmers, alternative concepts to convert chemical energy or heat into directed motion can be employed, which are potentially more efficient. The dynamics of microswimmers comprises many facets, which are all required to achieve locomotion. In this article, we review the physics of locomotion of biological and synthetic microswimmers, and the collective behavior of their assemblies. Starting from individual microswimmers, we describe the various propulsion mechanism of biological and synthetic systems and address the hydrodynamic aspects of swimming. This comprises synchronization and the concerted beating of flagella and cilia. In addition, the swimming behavior next to surfaces is examined. Finally, collective and cooperate phenomena of various types of isotropic and anisotropic swimmers with and without hydrodynamic interactions are discussed.
Nuclear pore complexes are constantly confronted by large fluxes of macromolecules and macromolecular complexes that need to get into and out of the nucleus. Such bi-directional traffic occurring in a narrow channel can easily lead to jamming. How th
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