- Letter
- Open Access
Physical interactions enable energy-efficient Turing patterns
Phys. Rev. Research 7, L042070 – Published 30 December, 2025
DOI: https://doi.org/10.1103/vtnv-2hw6
Abstract
Patterns are ubiquitous in nature, but how they form is often unclear. Turing developed a seminal theory to explain patterns based on reactions that counteract the equalizing tendency of diffusion. These reactions require continuous energy input since the system otherwise would proceed to equilibrium, but what systems are energy-efficient is currently unclear. To address this question, we introduce a thermodynamically consistent model of a Turing system. We reveal that repulsive interactions between the stereotypical activator and inhibitor reduce energy requirements significantly. Interestingly, efficient patterns occur for weak activity, albeit at reduced amplitude. Our results suggest that physical interactions might be central in forming natural patterns.
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References (39)
- F. Yuki, K. Hiroyasu, B. Kamran, and K. Aharon, Nanoscale Turing patterns in a bismuth monolayer, Nat. Phys. 17, 1031 (2021).
- P. Recho, A. Hallou, and E. Hannezo, Theory of mechanochemical patterning in biphasic biological tissues, Proc. Natl. Acad. Sci. USA 116, 5344 (2019).
- L. Goehring, Pattern formation in the geosciences, Philos. Trans. R. Soc. A 371, 20120352 (2013).
- A. M. Turing, The chemical basis of morphogenesis, Philos. Trans. R. Soc. Lond. B 237, 37 (1952).
- S. T. Vittadello, T. Leyshon, D. Schnoerr, and M. P. H. Stumpf, Turing pattern design principles and their robustness, Philos. Trans. R. Soc. A 379, 20200272 (2021).
- S. Kondo and T. Miura, Reaction-diffusion model as a framework for understanding biological pattern formation, Science 329, 1616 (2010).
- L. Menou, C. Luo, and D. Zwicker, Physical interactions in non-ideal fluids promote Turing patterns, J. R. Soc. Interface 20, 20230244 (2023).
- S. F. Banani, H. O. Lee, A. A. Hyman, and M. K. Rosen, Biomolecular condensates: Organizers of cellular biochemistry, Nat. Rev. Mol. Cell Biol. 18, 285 (2017).
- T. Y.-C. Tsai, R. M. Garner, and S. G. Megason, Adhesion-based self-organization in tissue patterning, Annu. Rev. Cell Dev. Biol. 38, 349 (2022).
- Q. X. Liu, A. Doelman, V. Rottschäfer, M. de Jager, P. M. J. Herman, M. Rietkerk, and J. van de Koppel, Phase separation explains a new class of self-organized spatial patterns in ecological systems. Proc. Natl. Acad. Sci. USA 110, 11905 (2013).
- G. L. Dignon, R. B. Best, and J. Mittal, Biomolecular phase separation: From molecular driving forces to macroscopic properties, Annu. Rev. Phys. Chem. 71, 53 (2020).
- See Supplemental Material at http://link.aps.org/supplemental/10.1103/vtnv-2hw6 for numerical details and additional calculations.
- J. W. Cahn and J. E. Hilliard, Free energy of a nonuniform system. I. Interfacial free energy, J. Chem. Phys. 28, 258 (1958).
- S. Safran, Statistical Thermodynamics of Surfaces, Interfaces and Membranes (CRC Press, Boca Raton, 2018).
- M. Rubinstein and R. H. Colby, Polymer Physics (Oxford University Press, Oxford, 2003), Vol. 23.
- P. Atkin and J. de Paula, Atkins’ Physical Chemistry, 9th ed. (W. H. Freeman & Company, New York, 2010), pp. 747–755.
- P. Hänggi, P. Talkner, and M. Borkovec, Reaction-rate theory: Fifty years after Kramers, Rev. Mod. Phys. 62, 251 (1990).
- I. Pagonabarraga, A. Pérez-Madrid, and J. M. Rubí, Fluctuating hydrodynamics approach to chemical reactions, Physica A 237, 205 (1997).
- M. Z. Bazant, Theory of chemical kinetics and charge transfer based on nonequilibrium thermodynamics, Acc. Chem. Res. 46, 1144 (2013).
- J. Kirschbaum and D. Zwicker, Controlling biomolecular condensates via chemical reactions, J. R. Soc. Interface 18, 20210255 (2021).
- D. Zwicker, The intertwined physics of active chemical reactions and phase separation, Curr. Opin. Colloid Interface Sci. 61, 101606 (2022).
- J. N. Weiss, The Hill equation revisited: Uses and misuses, FASEB J. 11, 835 (1997).
- J. Jorné, The effects of ionic migration on oscillations and pattern formation in chemical systems, J. Theor. Biol. 43, 375 (1974).
- N. Shigesada, K. Kawasaki, and E. Teramoto, Spatial segregation of interacting species, J. Theor. Biol. 79, 83 (1979).
- H. Malchow, Dissipative pattern formation in ternary non-linear reaction-electrodiffusion systems with concentration-dependent diffusivities, J. Theor. Biol. 135, 371 (1988).
- H. Malchow, A note on electrodiffusion and nonlinear reactions in heterogeneous media, Z. Phys. Chem. 271, 751 (1990).
- H. Malchow, Pattern formation in reaction-electrodiffusion systems with variable diffusivities and reaction rates, Physica A 213, 159 (1995).
- V. K. Vanag and I. R. Epstein, Cross-diffusion and pattern formation in reaction–diffusion systems, Phys. Chem. Chem. Phys. 11, 897 (2009).
- E. P. Zemskov, V. K. Vanag, and I. R. Epstein, Amplitude equations for reaction-diffusion systems with cross diffusion, Phys. Rev. E 84, 036216 (2011).
- E. A. Gaffney, A. L. Krause, P. K. Maini, and C. Wang, Spatial heterogeneity localizes Turing patterns in reaction-cross-diffusion systems, Discrete Contin. Dyn. Syst. B 28, 6092 (2023).
- A. Diez, A. L. Krause, P. K. Maini, E. A. Gaffney, and S. Seirin-Lee, Turing pattern formation in reaction-cross-diffusion systems with a bilayer geometry, Bull. Math. Biol. 86, 13 (2024).
- P. Kumar and G. Gangopadhyay, Nonequilibrium thermodynamics of glycolytic traveling wave: Benjamin-Feir instability, Phys. Rev. E 104, 014221 (2021).
- D. Zwicker, O. W. Paulin, and C. ter Burg, Physics of droplet regulation in biological cells, Rep. Prog. Phys. 88, 116601 (2025).
- J. Sastre, A. Thatte, A. M. Bergmann, M. Stasi, M. Tena-Solsona, C. A. Weber, and J. Boekhoven, Size control and oscillations of active droplets in synthetic cells, Nat. Commun. 16, 2003 (2025).
- F. Jülicher and C. A. Weber, Droplet physics and intracellular phase separation, Annu. Rev. Condens. Matter Phys. 15, 237 (2024).
- C. A. Weber, D. Zwicker, F. Jülicher, and C. F. Lee, Physics of active emulsions, Rep. Prog. Phys. 82, 064601 (2019).
- D. Zwicker, A. A. Hyman, and F. Jülicher, Suppression of Ostwald ripening in active emulsions. Phys. Rev. E 92, 012317 (2015).
- J. Söding, D. Zwicker, S. Sohrabi-Jahromi, M. Boehning, and J. Kirschbaum, Mechanisms of active regulation of biomolecular condensates, Trends Cell Biol. 30, 4 (2020).
- https://doi.org/10.5281/zenodo.17989458