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Explosive entrainment in Arnold tongues

Jiangsheng Wang1,2,3, Changgui Gu1,*, Wei Zou4, Haiying Wang1, Huijie Yang1, Ludovico Minati5,6,7,†, and Stefano Boccaletti8,9,10

  • *Contact author: gu_changgui@163.com
  • †Contact author: lminati@uestc.edu.cn; lminati@ieee.org

Phys. Rev. Research 7, 043156 – Published 12 November, 2025

DOI: https://doi.org/10.1103/9crr-yd6r

Abstract

Entrainment refers to the unidirectional synchronization of an oscillator system to external periodic forcing, with phase-locking regions forming Arnold tongues. In some specific models, the hysteresis phenomenon of Arnold tongue has been observed, but methods to actively induce it across models are still lacking. In this study, we show that adaptive responses to periodic forcing can induce explosive entrainment, a phenomenon of sudden locking to an external frequency accompanied by significant hysteresis. In contrast to explosive synchronization, where synchronization emerges suddenly due to internal coupling, explosive entrainment describes the sudden locking to a given frequency caused by external forcing. Therefore, explosive entrainment is more likely to occur in systems where internal couplings are weak or difficult to estimate, but external forcing can be applied. Furthermore, we demonstrate the universal emergence of explosive entrainment in the Kuramoto model, Poincaré model, chaotic Rössler model, and complex Ginzburg-Landau equation. Theoretical hysteresis bounds in the Kuramoto model are determined based on analytical results of the Ott-Antonsen reduction method. This study provides ideas for actively inducing hysteresis through external forcing.

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References (76)

  1. H. Zeng, Z. Qian, M. Myers, and M. Rosbash, A light-entrainment mechanism for the Drosophila circadian clock, Nature (London) 380, 129 (1996).
  2. U. Albrecht, Timing to perfection: The biology of central and peripheral circadian clocks, Neuron 74, 246 (2012).
  3. N. Mrosovsky and P. Salmon, A behavioural method for accelerating re-entrainment of rhythms to new light-dark cycles, Nature (London) 330, 372 (1987).
  4. D. C. Fernandez, R. Komal, J. Langel, J. Ma, P. Duy, M. Penzo, H. Zhao, and S. Hattar, Retinal innervation tunes circuits that drive nonphotic entrainment to food, Nature (London) 581, 194 (2020).
  5. P. Lakatos, J. Gross, and G. Thut, A new unifying account of the roles of neuronal entrainment, Curr. Biol. 29, R890 (2019).
  6. E. Bittman, Entrainment is NOT synchronization: An important distinction and its implications, J. Biol. Rhythms 36, 196 (2021).
  7. T. Fuchikawa, A. Eban-Rothschild, M. Nagari, Y. Shemesh, and G. Bloch, Potent social synchronization can override photic entrainment of circadian rhythms, Nat. Commun. 7, 11662 (2016).
  8. J. Prokkola and M. Nikinmaa, Circadian rhythms and environmental disturbances—Underexplored interactions, J. Exp. Biol. 221, jeb179267 (2018).
  9. B. Bano-Otalora, F. Martial, C. Harding, D. Bechtolda, A. Allen, T. Brown, M. Belle, and R. Lucas, Bright daytime light enhances circadian amplitude in a diurnal mammal, Proc. Natl. Acad. Sci. USA 118, e2100094118 (2021).
  10. Y. Murayama, H. Kori, C. Oshima, T. Kondo, H. Iwasaki, and H. Ito, Low temperature nullifies the circadian clock in cyanobacteria through Hopf bifurcation, Proc. Natl. Acad. Sci. USA 114, 5641 (2017).
  11. E. Buhr, S. Yoo, and J. Takahashi, Temperature as a universal resetting cue for mammalian circadian oscillators, Science 330, 379 (2010).
  12. K. Stokkan, S. Yamazaki, H. Tei, Y. Sakaki, and M. Menaker, Entrainment of the circadian clock in the liver by feeding, Science 291, 490 (2001).
  13. B. Zoefel, A. Archer-Boyd, and M. Davis, Phase entrainment of brain oscillations causally modulates neural responses to intelligible speech, Curr. Biol. 28, 401 (2018).
  14. A. Giraud and D. Poeppel, Cortical oscillations and speech processing: Emerging computational principles and operations, Nat. Neurosci. 15, 511 (2012).
  15. M. Somveille, M. Wikelski, R. Beyer, A. Rodrigues, A. Manica, and W. Jetz, Simulation-based reconstruction of global bird migration over the past 50 000 years, Nat. Commun. 11, 801 (2020).
  16. G. Pannella, Fish otoliths: Daily growth layers and periodical patterns, Science 173, 1124 (1971).
  17. A. Cresci, C. Paris, C. Durif, S. Shema, R. Bjelland, A. Skiftesvik, and H. Browman, Glass eels (Anguilla anguilla) have a magnetic compass linked to the tidal cycle, Sci. Adv. 3, e1602007 (2017).
  18. A. Jiménez, Y. Lu, A. Jambhekar, and G. Lahav, Principles, mechanisms and functions of entrainment in biological oscillators, Interface Focus 12, 20210088 (2022).
  19. V. Crunelli, M. Lőrincz, W. Connelly, F. David, S. Hughes, R. Lambert, N. Leresche, and A. Errington, Dual function of thalamic low-vigilance state oscillations: Rhythm-regulation and plasticity, Nat. Rev. Neurosci. 19, 107 (2018).
  20. S. Masri and P. Sassone-Corsi, Plasticity and specificity of the circadian epigenome, Nat. Neurosci. 13, 1324 (2010).
  21. R. Adler, A study of locking phenomena in oscillators, Proc. IRE 34, 351 (1946).
  22. V. I. Arnol’d, Small denominators. I. Mapping the circle onto itself, Izv. Ross. Akad. Nauk, Ser. Mat. 25, 21 (1961).
  23. H. González, H. Arce, and M. R. Guevara, Phase resetting, phase locking, and bistability in the periodically driven saline oscillator: Experiment and model, Phys. Rev. E 78, 036217 (2008).
  24. S. Nakata, K. Miyazaki, S. Izuhara, H. Yamaoka, and D. Tanaka, Arnold tongue of electrochemical nonlinear oscillators, J. Phys. Chem. A 113, 6876 (2009).
  25. C. M. Denis and P. François, Unclocklike oscillators with frequency memory for the entrainment of biological clocks, PRX Life 2, 043008 (2024).
  26. T. Antonsen, M. G. Faghih Jr., E. Ott, and J. Platig, External periodic driving of large systems of globally coupled phase oscillators, Chaos 18, 037112 (2008).
  27. L. Childs and S. Strogatz, Stability diagram for the forced Kuramoto model, Chaos 18, 043128 (2008).
  28. P. Poisson and K. D. Bhalerao, Hidden hysteresis—Population dynamics can obscure gene network dynamics, J. Biol. Eng. 7, 16 (2013).
  29. P. G. L. Sanchez, V. Mochulska, C. M. Denis, G. Mönke, T. Tomita, N. Tsuchida-Straeten, Y. Petersen, K. Sonnen, P. François, and A. Aulehla, Arnold tongue entrainment reveals dynamical principles of the embryonic segmentation clock, Elife 11, e79575 (2022).
  30. T. Lenc, P. E. Keller, M. Varlet, and S. Nozaradan, Neural and behavioral evidence for frequency-selective context effects in rhythm processing in humans, Cereb. Cortex Commun. 1, tgaa037 (2020).
  31. T. M. Lenton, H. Held, E. Kriegler, J. W. Hall, W. Lucht, S. Rahmstorf, and H. J. Schellnhuber, Tipping elements in the Earth’s climate system, Proc. Natl. Acad. Sci. USA 105, 1786 (2008).
  32. P. J. Menck, J. Heitzig, N. Marwan, and J. Kurths, How basin stability complements the linear-stability paradigm, Nat. Phys. 9, 89 (2013).
  33. X. Liu, D. Li, M. Ma, B. K. Szymanski, H. E. Stanley, and J. Gao, Network resilience, Phys. Rep. 971, 1 (2022).
  34. D. A. Golombek and R. E. Rosenstein, Physiology of circadian entrainment, Physiol. Rev. 90, 1063 (2010).
  35. Y. Kuramoto, Chemical Oscillations, Waves, and Turbulence (Springer-Verlag, Berlin, 1984).
  36. A. E. Motter, S. A. Myers, M. Anghel, and T. Nishikawa, Spontaneous synchrony in power-grid networks, Nat. Phys. 9, 191 (2013).
  37. L. Braga, A. Grinstein, M. Tardin, and M. Perin, Understanding reaction to corporate activism: The moderating role of polarization, PNAS Nexus 3, pgae313 (2024).
  38. S. Claessens, K. Fischer, A. Chaudhuri, C. Sibley, and Q. Atkinson, The dual evolutionary foundations of political ideology, Nat. Hum. Behav. 4, 336 (2020).
  39. K. Roecklein, P. Wong, N. Ernecoff, M. Miller, S. Donofry, M. Kamarck, W. Wood-Vasey, and P. Franzen, The post illumination pupil response is reduced in seasonal affective disorder, Psychiatry Res. 210, 150 (2013).
  40. M. Münch, L. Léon, S. Crippa, and A. Kawasaki, Circadian and wake-dependent effects on the pupil light reflex in response to narrow-bandwidth light pulses, Invest. Ophthalmol. Vis. Sci. 53, 4546 (2012).
  41. A. Kawasaki, S. Wisniewski, B. Healey, N. Pattyn, D. Kunz, M. Basner, and M. Münch, Impact of long-term daylight deprivation on retinal light sensitivity, circadian rhythms and sleep during the Antarctic winter, Sci. Rep. 8, 16185 (2018).
  42. M. Capello, M. Soria, P. Cotel, J-L. Deneubourg, and L. Dagorn, Quantifying the interplay between environmental and social effects on aggregated-fish dynamics, PLoS ONE 6, e28109 (2011).
  43. A. O. Kasumyan and D. S. Pavlov, Problems and prospects of studying schooling behavior of fish, J. Ichthyol. 63, 1393 (2023).
  44. A. Covanis, Photosensitivity in idiopathic generalized epilepsies, Epilepsia 46, 67 (2005).
  45. M. Q. Menétrey and D. Pascucci, Spectral tuning and after-effects in neural entrainment, Behav. Brain Funct. 20, 29 (2024).
  46. H. Sakaguchi, Cooperative phenomena in coupled oscillator systems under external fields, Prog. Theor. Phys. 79, 39 (1988).
  47. E. Ott and T. Antonsen, Low dimensional behavior of large systems of globally coupled oscillators, Chaos 18, 037113 (2008).
  48. X. Zhang, S. Boccaletti, S. Guan, and Z. Liu, Explosive synchronization in adaptive and multilayer networks, Phys. Rev. Lett. 114, 038701 (2015).
  49. J. Wang, C. Gu, and W. Zou, Rhythmic states and first-order phase transitions in adaptive coupled three-dimensional limit-cycle oscillators, Phys. Rev. E 110, 044209 (2024).
  50. See Supplemental Material at http://link.aps.org/supplemental/10.1103/9crr-yd6r for more numerical simulation details.
  51. S. H. Strogatz and R. E. Mirollo, Stability of incoherence in a population of coupled oscillators, J. Stat. Phys. 63, 613 (1991).
  52. T. Stankovski, T. Pereira, P. V. McClintock, and A. Stefanovska, Coupling functions: Universal insights into dynamical interaction mechanisms, Rev. Mod. Phys. 89, 045001 (2017).
  53. C. Gu and H. Yang, The asymmetry of the entrainment range induced by the difference in intrinsic frequencies between two subgroups within the suprachiasmatic nucleus, Chaos 27, 063115 (2017).
  54. C. Gu and H. Yang, Differences in intrinsic amplitudes of neuronal oscillators improve synchronization in the suprachiasmatic nucleus, Chaos 27, 093108 (2017).
  55. C. Gu, H. Yang, M. Wang, and J. H. Rohling, Heterogeneity in relaxation rate improves the synchronization of oscillatory neurons in a model of the SCN, Chaos 29, 013103 (2019).
  56. O. E. Rössler, An equation for continuous chaos, Phys. Lett. A 57, 397 (1976).
  57. A. Pikovsky, M. Rosenblum, G. Osipov, and J. Kurths, Phase synchronization of chaotic oscillators by external driving, Phys. D 104, 219 (1997).
  58. M. Zaks, E. Park, M. Rosenblum, and J. Kurths, Alternating locking ratios in imperfect phase synchronization, Phys. Rev. Lett. 82, 4228 (1999).
  59. A. E. Hramov, A. A. Koronovskii, and P. V. Popov, Generalized synchronization in coupled Ginzburg-Landau equations and mechanisms of its arising, Phys. Rev. E 72, 037201 (2005).
  60. B. Thakur and A. Sen, Collective dynamics of globally delay-coupled complex Ginzburg-Landau oscillators, Chaos 29, 053104 (2019).
  61. M.-L. Chabanol, V. Hakim, and W.-J. Rappel, Collective chaos and noise in the globally coupled complex Ginzburg-Landau equation, Phys. D 103, 273 (1997).
  62. A. Golden, A. E. Sgro, and P. Mehta, Arnold tongues in oscillator systems with nonuniform spatial driving, Phys. Rev. E 103, 042211 (2021).
  63. S. Boccaletti, J. A. Almendral, S. Guan, I. Leyva, Z. Liu, I. Sendiña-Nadal, Z. Wang, and Y. Zou, Explosive transitions in complex networks’ structure and dynamics: Percolation and synchronization, Phys. Rep. 660, 1 (2016).
  64. J. Gómez-Gardeñes, S. Gómez, A. Arenas, and Y. Moreno, Explosive synchronization transitions in scale-free networks, Phys. Rev. Lett. 106, 128701 (2011).
  65. J. Wang, C. Gu, and P. Ji, Frequency-amplitude correlation inducing first-order phase transition in coupled oscillators, New J. Phys. 24, 073038 (2022).
  66. J. Wang, C. Gu, Y. Xu, and W. Zou, Discontinuous phase transition switching induced by a power-law function between dynamical parameters in coupled oscillators, Chaos 34, 023106 (2024).
  67. Z. Lu, K. Klein-Cardeña, S. Lee, T. Antonsen, M. Girvan, and E. Ott, Resynchronization of circadian oscillators and the east-west asymmetry of jet-lag, Chaos 26, 094811 (2016).
  68. J. Lucero, J. Schoentgen, J. Haas, P. Luizard, and X. Pelorson, Self-entrainment of the right and left vocal fold oscillators, J. Acoust. Soc. Am. 137, 2036 (2015).
  69. A. Sahay, A. Roy, S. A. Pawar, and R. I. Sujith, Dynamics of coupled thermoacoustic oscillators under asymmetric forcing, Phys. Rev. Appl. 15, 044011 (2021).
  70. M. Ghil and V. Lucarini, The physics of climate variability and climate change, Rev. Mod. Phys. 92, 035002 (2020).
  71. D. Witthaut, F. Hellmann, J. Kurths, S. Kettemann, H. Meyer-Ortmanns, and M. Timme, Collective nonlinear dynamics and self-organization in decentralized power grids, Rev. Mod. Phys. 94, 015005 (2022).
  72. Z. Ma, Y. Luo, C. Zeng, and B. Zheng, Spatiotemporal diffusion as early warning signal for critical transitions in spatial tumor-immune system with stochasticity, Phys. Rev. Res. 4, 023039 (2022).
  73. A. C.-L. Chian, P. R. Muñoz, and E. L. Rempel, Edge of chaos and genesis of turbulence, Phys. Rev. E 88, 052910 (2013).
  74. J. A. C. Gallas, Structure of the parameter space of the Hénon map, Phys. Rev. Lett. 70, 2714 (1993).
  75. R. A. Miranda, E. L. Rempel, and A. C. -L. Chian, Chaotic saddles in nonlinear modulational interactions in a plasma, Phys. Plasmas 19, 112303 (2012).
  76. R. Rajni and B. Ghosh, Arnold tongues, shrimp structures, multistability, and ecological paradoxes in a discrete-time predator-prey system, Chaos 34, 123103 (2024).

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