» Articles » PMID: 21865254

Emergence of Coherent Structures and Large-scale Flows in Motile Suspensions

Overview
Date 2011 Aug 26
PMID 21865254
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

The emergence of coherent structures, large-scale flows and correlated dynamics in suspensions of motile particles such as swimming micro-organisms or artificial microswimmers is studied using direct particle simulations. A detailed model is proposed for a slender rod-like particle that propels itself in a viscous fluid by exerting a prescribed tangential stress on its surface, and a method is devised for the efficient calculation of hydrodynamic interactions in large-scale suspensions of such particles using slender-body theory and a smooth particle-mesh Ewald algorithm. Simulations are performed with periodic boundary conditions for various system sizes and suspension volume fractions, and demonstrate a transition to large-scale correlated motions in suspensions of rear-actuated swimmers, or Pushers, above a critical volume fraction or system size. This transition, which is not observed in suspensions of head-actuated swimmers, or Pullers, is seen most clearly in particle velocity and passive tracer statistics. These observations are consistent with predictions from our previous mean-field kinetic theory, one of which states that instabilities will arise in uniform isotropic suspensions of Pushers when the product of the linear system size with the suspension volume fraction exceeds a given threshold. We also find that the collective dynamics of Pushers result in giant number fluctuations, local alignment of swimmers and strongly mixing flows. Suspensions of Pullers, which evince no large-scale dynamics, nonetheless display interesting deviations from the random isotropic state.

Citing Articles

Transcription-dependent mobility of single genes and genome-wide motions in live human cells.

Chu F, Clavijo A, Lee S, Zidovska A Nat Commun. 2024; 15(1):8879.

PMID: 39438437 PMC: 11496510. DOI: 10.1038/s41467-024-51149-4.


Bacterial bioconvection confers context-dependent growth benefits and is robust under varying metabolic and genetic conditions.

Shoup D, Ursell T J Bacteriol. 2023; 205(10):e0023223.

PMID: 37787517 PMC: 10601612. DOI: 10.1128/jb.00232-23.


Gyrotactic cluster formation of bottom-heavy squirmers.

Ruhle F, Zantop A, Stark H Eur Phys J E Soft Matter. 2022; 45(3):26.

PMID: 35304659 PMC: 8933315. DOI: 10.1140/epje/s10189-022-00183-5.


Imaging the emergence of bacterial turbulence: Phase diagram and transition kinetics.

Peng Y, Liu Z, Cheng X Sci Adv. 2021; 7(17).

PMID: 33893094 PMC: 8064640. DOI: 10.1126/sciadv.abd1240.


Active fluid with Acidithiobacillus ferrooxidans: correlations between swimming and the oxidation route.

Torrenegra J, Agudelo-Morimitsu L, Marquez-Godoy M, Hernandez-Ortiz J J Biol Phys. 2019; 45(2):193-211.

PMID: 31073789 PMC: 6548800. DOI: 10.1007/s10867-019-09524-6.


References
1.
Tuval I, Cisneros L, Dombrowski C, Wolgemuth C, Kessler J, Goldstein R . Bacterial swimming and oxygen transport near contact lines. Proc Natl Acad Sci U S A. 2005; 102(7):2277-82. PMC: 548973. DOI: 10.1073/pnas.0406724102. View

2.
Wolgemuth C . Collective swimming and the dynamics of bacterial turbulence. Biophys J. 2008; 95(4):1564-74. PMC: 2483759. DOI: 10.1529/biophysj.107.118257. View

3.
Hohenegger C, Shelley M . Stability of active suspensions. Phys Rev E Stat Nonlin Soft Matter Phys. 2010; 81(4 Pt 2):046311. DOI: 10.1103/PhysRevE.81.046311. View

4.
Paxton W, Kistler K, Olmeda C, Sen A, St Angelo S, Cao Y . Catalytic nanomotors: autonomous movement of striped nanorods. J Am Chem Soc. 2004; 126(41):13424-31. DOI: 10.1021/ja047697z. View

5.
Baskaran A, Marchetti M . Statistical mechanics and hydrodynamics of bacterial suspensions. Proc Natl Acad Sci U S A. 2009; 106(37):15567-72. PMC: 2747162. DOI: 10.1073/pnas.0906586106. View