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Talia Calazans

Publications and source records attributed to Talia Calazans.

3 recordsLinked to original sources

The Countoscope for self-propelled particles

Particle number fluctuations $N(t)$, measured in virtual observation boxes of an image or a simulation, offer a way to quantify particle dynamics when particle tracking is impractical, such as in high-density systems. While traditionally limited to equilibrium diffusive systems, we extend this approach -- named ``Countoscope'' -- to out-of-equilibrium self-propelled particles: Active Brownian (ABPs), Run and Tumble (RTPs), and Active Ornstein-Uhlenbeck Particles (AOUPs). For AOUPs, we leverage their Gaussian statistics to derive a general formula applicable to any Gaussian system. For ABPs and RTPs, we derive the intermediate scattering function (ISF) -- and thus the correlations of $N(t)$ -- using an exact perturbative expansion over the probability density fields, revealing key physical features of the ISF and of the number correlations. Our theoretical predictions for the mean-squared number difference $\langle \Delta N^2(t) \rangle = \langle (N(t) - N(0))^2 \rangle$ match stochastic simulations and exhibit three time-dependent scaling regimes: diffusive, advective, and long-time enhanced diffusive, reflecting the regimes of the mean squared particle displacement. We further uncover limiting laws in each of these regimes that are useful to quantify self-propulsion properties.

cond-mat.soft

Biomedical active matter: Emergence and breakdown of collective functionalities

Living systems are made of active materials with microscopic components that work together to perform macroscopic biological tasks. The breakdown of these collective functionalities leads to diseases, which, conversely, could be treated by exploiting self-organization in healthcare technologies. Here, we review recent advances in this rapidly growing field of biomedical active matter. The main themes are (1) collective self-assembly and spatiotemporal coordination; (2) collective motion, transport, and navigation; (3) collective sensing, signaling, and communication; and (4) collective adaptation, evolution, and learning. We discuss these emerging processes in a wide range of systems, including protein folding, biomolecular condensates, cytoskeleton dynamics, intracellular flows, bacterial biofilms, quorum sensing, cilia synchronization, wound healing, biolocomotion, neurons, endocrine signalling, and cardiovascular flow networks. For each, we highlight medical conditions associated with reduced collective functionality and how they may be treated using microrobotic swarms, bioinspired metamaterials, diagnostics, lab-on-chip devices, organoids, and other active and adaptive matter innovations.

physics.bio-ph

Surfing on metachronal waves: ciliary transport by inertial coasting

Motile cilia drive biological fluid transport through whip-like beating motions that synchronize into metachronal waves. The lengths of these cilia span three orders of magnitude, from microns in human airways to millimeters in ctenophores. While recent studies have considered ciliary flows at intermediate Reynolds numbers, the effect of inertia on coordinated particle transport remains unexplored. Here, we address this gap using "Pufflets," the inertial counterparts of Stokeslets. These Pufflets describe rapidly accelerating flows generated by short-lived impulses, encoded by spatiotemporally singular momentum injections. To produce such rapid impulses experimentally, we designed an Atwood machine that generates long-lived Pufflet flows, which we capture with high-speed PIV measurements that agree well with analytical theory and simulations. Moreover, we find that pairs of equal and opposite Pufflets can drive net particle displacements and mixing due to time reversal symmetry breaking, which would be impossible in Stokes flow. Finally, we consider metachronal waves of Pufflets. Remarkably, we discover that particles can surf on these waves by coasting inertially from one cilium to the next, leading to highly efficient particle transport. This work paves the way toward understanding rapidly accelerating flows and collective transport driven by biological and artificial cilia.

physics.bio-ph