journal article·2016-01

Mechanics of fire ant aggregations

Michael Tennenbaum, Zhongyang Liu, David Hu, Alberto Fernandez-Nieves

Nature Materials· Volume 15· Issue 1
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Abstract

Fire ants link their bodies to form aggregations; these can adopt a variety of structures, they can drip and spread, or withstand applied loads. Here, by using oscillatory rheology, we show that fire ant aggregations are viscoelastic. We find that, at the lowest ant densities probed and in the linear regime, the elastic and viscous moduli are essentially identical over the spanned frequency range, which highlights the absence of a dominant mode of structural relaxation. As ant density increases, the elastic modulus rises, which we interpret by alluding to ant crowding and subsequent jamming. When deformed beyond the linear regime, the aggregation flows, exhibiting shear-thinning behaviour with a stress load that is comparable to the maximum load the aggregation can withstand before individual ants are torn apart. Our findings illustrate the rich, collective mechanical behaviour that can arise in aggregations of active, interacting building blocks.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Insect and Arachnid Ecology and Behavior · Micro and Nano Robotics · Ecosystem dynamics and resilience

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (30)

Show source-provided references
1. Anderson, C., Theraulaz, G. & Deneubourg, J.-L. Self-assemblages in insect societies. Insect. Soc. 49, 99–110 (2002).10.1007/s00040-002-8286-y ↗
2. Bonabeau, E. et al. Dripping faucet with ants. Phys. Rev. E 57, 5904–5907 (1998).
3. Hölldobler, B. The Ants (Harvard Univ. Press, 1990).10.1007/978-3-662-10306-7 ↗
4. Mlot, N. J., Tovey, C. A. & Hu, D. L. Fire ants self-assemble into waterproof rafts to survive floods. Proc. Natl Acad. Sci. USA 108, 7669–7673 (2011).10.1073/pnas.1016658108 ↗
5. Foster, P. C., Mlot, N. J., Lin, A. & Hu, D. L. Fire ants actively control spacing and orientation within self-assemblages. J. Exp. Biol. 217, 2089–2100 (2014).10.1242/jeb.093021 ↗
6. Schneirla, T. C. Army Ants: A Study in Social Organization (W. H. Freeman, 1971).
7. Winter, H. H. & Mours, M. Neutron Spin Echo Spectroscopy Viscoelasticity Rheology 165–234 (Springer, 1997).10.1007/3-540-68449-2_3 ↗
8. Chhabra, R. P. Bubbles, Drops, and Particles in Non-Newtonian Fluids (CRC Press, 2006).10.1201/9781420015386 ↗
9. Zill, S. N., Chaudhry, S., Büschges, A. & Schmitz, J. Directional specificity and encoding of muscle forces and loads by stick insect tibial campaniform sensilla, including receptors with round cuticular caps. Arth. Struct. Dev. 42, 455–467 (2013).10.1016/j.asd.2013.10.001 ↗
10. Couzin, I. D. & Krause, J. in Advances in the Study of Behavior Vol. 32, 1–75 (Academic Press, 2003).
11. Sumpter, D. J. The principles of collective animal behaviour. Phil. Trans. R Soc. Lond. B 361, 5–22 (2006).10.1098/rstb.2005.1733 ↗
12. Alcaraz, J. et al. Microrheology of human lung epithelial cells measured by atomic force microscopy. Biophys. J. 84, 2071–2079 (2003).10.1016/S0006-3495(03)75014-0 ↗
13. Gisler, T. & Weitz, D. A. Scaling of the microrheology of semidilute F-actin solutions. Phys. Rev. Lett. 82, 1606 (1999).10.1103/PhysRevLett.82.1606 ↗
14. Marchetti, M. C. Active matter: Spontaneous flows and self-propelled drops. Nature 491, 340–341 (2012).10.1038/nature11750 ↗
15. Sanchez, T., Chen, D. T. N., DeCamp, S. J., Heymann, M. & Dogic, Z. Spontaneous motion in hierarchically assembled active matter. Nature 491, 431–434 (2012).10.1038/nature11591 ↗
16. Stone, M. & Goldbart, P. Mathematics for Physics: A Guided Tour for Graduate Students (Cambridge Univ. Press, 2009).10.1017/CBO9780511627040 ↗
17. Bird, R. B., Armstrong, R. C. & Hassager, O. Dynamics of Polymeric Liquids, Fluid Mechanics 2nd edn (Wiley, 1987).
18. Winter, H. H. & Chambon, F. Analysis of linear viscoelasticity of a crosslinking polymer at the gel point. J. Rheol. 30, 367–382 (1986).10.1122/1.549853 ↗
19. Krall, A. H. & Weitz, D. A. Internal dynamics and elasticity of fractal colloidal gels. Phys. Rev. Lett. 80, 778–781 (1998).10.1103/PhysRevLett.80.778 ↗
20. Fabry, B. et al. Scaling the microrheology of living cells. Phys. Rev. Lett. 87, 148102 (2001).10.1103/PhysRevLett.87.148102 ↗
21. Ng, T. S. K. & McKinley, G. H. Power law gels at finite strains: The nonlinear rheology of gluten gels. J. Rheol. 52, 417 (2008).10.1122/1.2828018 ↗
22. Trappe, V. & Sandkühler, P. Colloidal gels—low-density disordered solid-like states. Curr. Opin. Colloid Interface Sci. 8, 494–500 (2004).10.1016/j.cocis.2004.01.002 ↗
23. Mason, T., Bibette, J. & Weitz, D. Elasticity of compressed emulsions. Phys. Rev. Lett. 75, 2051–2054 (1995).10.1103/PhysRevLett.75.2051 ↗
24. Angelini, T. E. et al. Glass-like dynamics of collective cell migration. Proc. Natl Acad. Sci. USA 108, 4714–4719 (2011).10.1073/pnas.1010059108 ↗
25. Berthier, L. Nonequilibrium glassy dynamics of self-propelled hard disks. Phys. Rev. Lett. 112, 220602 (2014).10.1103/PhysRevLett.112.220602 ↗
26. Gonzalez-Rodriguez, D., Guevorkian, K., Douezan, S. & Brochard-Wyart, F. Soft matter models of developing tissues and tumors. Science 338, 910–917 (2012).10.1126/science.1226418 ↗
27. Ni, R., Stuart, M. A. C. & Dijkstra, M. Pushing the glass transition towards random close packing using self-propelled hard spheres. Nature Commun. 4, 2704 (2013).10.1038/ncomms3704 ↗
28. Rubenstein, M., Cornejo, A. & Nagpal, R. Programmable self-assembly in a thousand-robot swarm. Science 345, 795–799 (2014).10.1126/science.1254295 ↗
29. Werfel, J., Petersen, K. & Nagpal, R. Designing collective behavior in a termite-inspired robot construction team. Science 343, 754–758 (2014).10.1126/science.1245842 ↗
30. Janmey, P. A. & Weitz, D. A. Dealing with mechanics: Mechanisms of force transduction in cells. Trends Biochem. Sci. 29, 364–370 (2004).10.1016/j.tibs.2004.05.003 ↗