Circadian Rhythm Adaptation Mechanisms in Extreme Environments
DOI:
https://doi.org/10.61173/ee36ns36Keywords:
Circadian Clock, Extreme Environments, TemperatureAbstract
Circadian rhythms coordinate physiology and behavior across species, yet on extreme photoperiodic cycles, in polar regions, in spaceflight, and deep sea, and in thermally extreme habitats, photic entrainment is disturbed. This review attempts to draw together evidence for clocks functioning well when light cues are unreliable; in doing this, it emphasizes non-photic Zeitgebers and molecular plasticity. The studies cite temperature cycles, altered gravity, feeding and social schedules, and magnetic inputs in terms of their abilities to entrain central and peripheral oscillators. We highlight at the molecular level epigenetic remodeling (DNA methylation, histone marks, and chromatin accessibility), non-coding RNAs, and posttranslational modifications as the key mechanisms that under stress retune the CLOCK: BMAL1–PER/CRY feedback loops in metabolism and immunity. A comparative appraisal includes polar vertebrates maintaining rhythms in continuous light/darkness via thermal and seasonal signals; astronauts and model organisms adapting in microgravity with desynchronized tissue clocks and altered neurocardiac dynamics; and desert, polar marine, and deep-sea species responding to temperature, tidal, and lunar cycles. Overall, these findings reveal the flexible multi-cue architecture for temporal organization that directly pertains to human health and performance concerns in polar operations and long-duration spaceflight, as well as ecological resilience in rapid environmental change. The journey into how clocks reweight non-photic inputs and engage epigenetic flexibility underpins countermeasures (light, temperature, feeding schedules), which could lead to conservation methods aimed at reestablishing rhythmicity during conditions when photic cues become dysfunctional.
References
[1] Timothy Howard Monk, Daniel Joseph Buysse, Bart David Billy, Kathy Sue Kennedy, Linda Marie Willrich. Sleep and circadian rhythms in four orbiting astronauts. Journal of Biological Rhythms, 1998, 13(3): 188–201.
[2] Cory Todd Williams, Brian Mark Barnes, Lily Yan, Charles Loren Buck. Entraining to the polar day: circadian rhythms in arctic ground squirrels. Journal of Experimental Biology, 2017, 220: 3095–3102. https://doi.org/10.1242/jeb.159889 Dean&Francis Zihan Guo
[3] Jenni Maria Prokkola, Mikko Nikinmaa. Circadian rhythms and environmental disturbances – underexplored interactions. Journal of Experimental Biology, 2018, 221: jeb179267. https:// doi.org/10.1242/jeb.179267
[4] Cory Todd Williams, Brian Mark Barnes, Charles Loren Buck. Persistence, entrainment, and function of circadian rhythms in polar vertebrates. Physiology, 2015, 30(5): 258–269. https://doi.org/10.1152/physiol.00045.2014
[5] David George Hazlerigg, Daniel Appenroth, Barbara Maria Tomotani, Alexander Charles West, Shona Helen Wood. Biological timekeeping in polar environments: lessons from terrestrial vertebrates. Journal of Experimental Biology, 2023, 226: jeb246308. https://doi.org/10.1242/jeb.246308
[6] Hongjie Zong, Yifei Fei, Ningang Li. Circadian disruption and sleep disorders in astronauts: a review of multi-disciplinary interventions for long-duration space missions. International Journal of Molecular Sciences, 2025, 26(11): 5179. https://doi. org/10.3390/ijms26115179
[7] Bin Wu, Yue Wang, Xiaorui Wu, Dong Liu, Dong Xu, Fei Wang. On-orbit sleep problems of astronauts and countermeasures. Military Medical Research, 2018, 5: 17. https://doi.org/10.1186/s40779-018-0165-6
[8] Ricardo Orozco-Solis, Lorena Aguilar-Arnal. Circadian regulation of immunity through epigenetic mechanisms. Frontiers in Cellular and Infection Microbiology, 2020, 10: 96. https://doi.org/10.3389/fcimb.2020.00096
[9] Hiroaki Taniguchi, Agustin Federico Fernández, Fernando Setién, Santiago Ropero, Esteban Ballestar, Alberto Villanueva, Hiroyuki Yamamoto, Kohzoh Imai, Yasuhisa Shinomura, Manel Esteller. Epigenetic inactivation of the circadian clock gene BMAL1 in hematologic malignancies. Cancer Research, 2009, 69(21): 8447–8454.
[10] Marina Maria Bellet, Paolo Sassone-Corsi. Mammalian circadian clock and metabolism – the epigenetic link. Journal of Cell Science, 2010, 123(24): 3837–3848. https://doi. org/10.1242/jcs.051649
[11] Jeffrey Scott Adelman, Lynn Bixby Martin. Stress and disease ecology: A behavioral ecological approach. Integrative and Comparative Biology, 2009, 49(3): 202–214. https://doi. org/10.1093/icb/icp028
[12] Robert Morris Sapolsky. Why Zebras Don’t Get Ulcers (3rd ed.). Holt Paperbacks, 2004.
[13] Joseph E. LeDoux. Rethinking the emotional brain. Neuron, 2012, 73(4): 653–676. https://doi.org/10.1016/ j.neuron.2012.02.004
[14] Emma Jane Harding, Elizabeth Sarah Paul, Michael Mendl. Animal behaviour: Cognitive bias and affective state. Nature, 2004, 427(6972): 312. https://doi.org/10.1038/427312a
Downloads
Published
Issue
Section
License
Copyright (c) 2025 by the authors.

This work is licensed under a Creative Commons Attribution 4.0 International License.
