Noise

Noise-Induced Resonance in Periodically Driven Run-and-Tumble Bacterial Suspensions

Authors

Keywords:

Active matter, Stochastic resonance, Density-dependent motility, Collective dynamics, Particle-based simulation

Abstract

Noise is generally regarded as a source of disorder in active matter, yet its role in periodically driven bacterial suspensions remains poorly understood. Here, we use particle-based simulations to investigate whether stochastic tumbling can enhance the collective response of a quasi-two-dimensional suspension of run-and-tumble bacteria subjected to weak periodic motility modulation. The unforced system exhibits a transition from a homogeneous active fluid to a clustered state below a critical tumbling rate of approximately 0.42 s⁻¹, establishing the intrinsic relaxation timescale of the suspension. Under subthreshold forcing, the structural response displays a clear resonance at an intermediate tumbling rate, where the active-pressure oscillation increases by approximately 5.4-fold and the mechanical hysteresis area by 4.6-fold relative to the low-noise state. Increasing temperature shifts the optimal tumbling rate from 0.26 to 1.30 s⁻¹, reduces the maximum structural response by about 94%, and shortens the relaxation time by more than one order of magnitude. Nevertheless, both structural and mechanical responses collapse onto universal master curves when expressed as a function of  demonstrating that collective synchronization is governed by relaxation-time matching between stochastic tumbling and periodic forcing. These findings provide a simple framework for controlling organization and mechanical response in active bacterial suspensions.

Dimensions

Arlt, J., Martinez, V. A., Dawson, A., Pilizota, T., & Poon, W. C. K. (2018). Painting with light-powered bacteria. Nature Communications, 9, Article 768. https://doi.org/10.1038/s41467-018-03161-8 DOI: https://doi.org/10.1038/s41467-018-03161-8

Baconnier, P., Démery, V., & Dauchot, O. (2024). Noise-induced collective actuation in active solids. Physical Review E, 109(2), 024606. https://doi.org/10.1103/PhysRevE.109.024606 DOI: https://doi.org/10.1103/PhysRevE.109.024606

Bäuerle, T., Fischer, A., Speck, T., & Bechinger, C. (2018). Self-organization of active particles by quorum-sensing rules. Nature Communications, 9, Article 3232. https://doi.org/10.1038/s41467-018-05675-7 DOI: https://doi.org/10.1038/s41467-018-05675-7

Caprini, L., Marconi, U. M. B., Puglisi, A., & Vulpiani, A. (2020). Active escape dynamics: The effect of persistence on barrier crossing. Journal of Statistical Mechanics: Theory and Experiment, 2020(5), 053203. https://doi.org/10.1088/1742-5468/ab7c5f DOI: https://doi.org/10.1088/1742-5468/ab14dd

Cates, M. E., & Tailleur, J. (2015). Motility-induced phase separation. Annual Review of Condensed Matter Physics, 6, 219–244. https://doi.org/10.1146/annurev-conmatphys-031214-014710 DOI: https://doi.org/10.1146/annurev-conmatphys-031214-014710

Digregorio, P., Levis, D., Suma, A., Cugliandolo, L. F., Gonnella, G., & Pagonabarraga, I. (2018). Full phase diagram of active Brownian disks: From melting to motility-induced phase separation. Physical Review Letters, 121(9), 098003. https://doi.org/10.1103/PhysRevLett.121.098003 DOI: https://doi.org/10.1103/PhysRevLett.121.098003

Dubay, M. M., Johnston, N., Wronkiewicz, M., Lee, J., Lindensmith, C. A., & Nadeau, J. L. (2022). Quantification of motility in Bacillus subtilis at temperatures up to 84°C using a submersible volumetric microscope and automated tracking. Frontiers in Microbiology, 13, Article 836808. https://doi.org/10.3389/fmicb.2022.836808 DOI: https://doi.org/10.3389/fmicb.2022.836808

Gammaitoni, L., Hänggi, P., Jung, P., & Marchesoni, F. (1998). Stochastic resonance. Reviews of Modern Physics, 70(1), 223–287. https://doi.org/10.1103/RevModPhys.70.223 DOI: https://doi.org/10.1103/RevModPhys.70.223

Solon, A. P., Fily, Y., Baskaran, A., Cates, M. E., Kafri, Y., Kardar, M., & Tailleur, J. (2015). Pressure is not a state function for generic active fluids. Nature Physics, 11(8), 673–678. https://doi.org/10.1038/nphys3374 DOI: https://doi.org/10.1038/nphys3377

Stenhammar, J., Marenduzzo, D., Allen, R. J., & Cates, M. E. (2014). Phase behaviour of active Brownian particles: The role of dimensionality. Soft Matter, 10(10), 1489–1499. https://doi.org/10.1039/C3SM52813H DOI: https://doi.org/10.1039/C3SM52813H

Tailleur, J., & Cates, M. E. (2008). Statistical mechanics of interacting run-and-tumble bacteria. Physical Review Letters, 100(21), 218103. https://doi.org/10.1103/PhysRevLett.100.218103 DOI: https://doi.org/10.1103/PhysRevLett.100.218103

Takatori, S. C., Yan, W., & Brady, J. F. (2014). Swim pressure: Stress generation in active matter. Physical Review Letters, 113(2), 028103. https://doi.org/10.1103/PhysRevLett.113.028103 DOI: https://doi.org/10.1103/PhysRevLett.113.028103

Zheng, C., & Tönjes, R. (2022). Noise-induced swarming of active particles. Physical Review E, 106(6), 064601. https://doi.org/10.1103/PhysRevE.106.064601 DOI: https://doi.org/10.1103/PhysRevE.106.064601

Published

2026-08-03

How to Cite

Igwe, I. E. (2026). Noise: Noise-Induced Resonance in Periodically Driven Run-and-Tumble Bacterial Suspensions. Nigerian Journal of Theoretical and Environmental Physics, 1(1), 80-89. https://doi.org/10.62292/njtep.v1i1.2023.149

How to Cite

Igwe, I. E. (2026). Noise: Noise-Induced Resonance in Periodically Driven Run-and-Tumble Bacterial Suspensions. Nigerian Journal of Theoretical and Environmental Physics, 1(1), 80-89. https://doi.org/10.62292/njtep.v1i1.2023.149

Most read articles by the same author(s)