Acute temperature effects on cilia beating increase coral deoxygenation
4 affiliations
- 1Marine Biology Section, Department of Biology, University of Copenhagen, Strandpromenaden 5, Helsingør, Denmark
- 2Marine Science Program, Biological and Environmental Science and Engineering Division, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia
- 3School of Mathematics and Statistics, The University of Melbourne, Parkville, Victoria, Australia
- 4IOW Leibniz-Institute for Baltic Sea Research, Warnemünde, Rostock, Germany
Abstract
Cilia-induced vortical flows are critical for regulating oxygen (O 2 ) and metabolite exchange across coral-water interfaces. While this active ventilation affects the coral tissue microenvironment, its role in thermal stress remains poorly understood. Using high-speed imaging of cilia beating, particle image velocimetry with O 2 -sensitive nanoparticles, and a mechanistic transport model, we quantified how ciliary dynamics in the reef-building coral Porites lutea respond to acute warming in darkness. Moderate warming (~35°C) enhanced ciliary activity and advective transport yet paradoxically thickened the concentration boundary layer with O 2 -depleted water, exposing tissues to transient hypoxia. At higher temperatures, ventilation failed to meet rising metabolic demands and anoxic regions expanded rapidly. Above ~37°C, ciliary coordination collapsed and vortical flows dissipated, shifting transport to a diffusion-limited regime accelerating coral mortality. These results identify ciliary beating as a key regulator of thermal tolerance and early indicator of critical physiological tipping points for reef-building corals in a warming, deoxygenating ocean.
Related
- An Analog-Sensitive Tau Tubulin Kinase 2 Enables Acute Chemical-Genetic Control of Primary Cilia
- Historical squid biomass increase is not explained by rising temperature but rather by loss of top predators.
- Comprehensive transcriptome-wide characterisation of hepatopancreas in response to acute low-temperature stress in Macrobrachium rosenbergii
- In vivo optical induction of INaL by photoactivation of AaH-II peptide in beating heart using wireless implantable device
- Standardizing deoxygenation studies in coral biology
BibTeX
@article{pacherres2026acute,
title = {{Acute temperature effects on cilia beating increase coral deoxygenation}},
author = {César O. Pacherres and Max S. Dhillon and Mads Bilbo and Mikkel Hansen and Douglas R. Brumley and Manuel Aranda and Soeren Ahmerkamp and Michael Kühl},
journal = {Science Advances},
year = {2026},
month = may,
doi = {10.1126/sciadv.aeg0950},
url = {https://doi.org/10.1126/sciadv.aeg0950},
note = {CC BY-NC},
}
RIS
TY - JOUR
TI - Acute temperature effects on cilia beating increase coral deoxygenation
AU - César O. Pacherres
AU - Max S. Dhillon
AU - Mads Bilbo
AU - Mikkel Hansen
AU - Douglas R. Brumley
AU - Manuel Aranda
AU - Soeren Ahmerkamp
AU - Michael Kühl
PY - 2026
DA - 2026/05/20
JO - Science Advances
DO - 10.1126/sciadv.aeg0950
UR - https://doi.org/10.1126/sciadv.aeg0950
AB - Cilia-induced vortical flows are critical for regulating oxygen (O 2 ) and metabolite exchange across coral-water interfaces. While this active ventilation affects the coral tissue microenvironment, its role in thermal stress remains poorly understood. Using high-speed imaging of cilia beating, particle image velocimetry with O 2 -sensitive nanoparticles, and a mechanistic transport model, we quantified how ciliary dynamics in the reef-building coral Porites lutea respond to acute warming in darkness. Moderate warming (~35°C) enhanced ciliary activity and advective transport yet paradoxically thickened the concentration boundary layer with O 2 -depleted water, exposing tissues to transient hypoxia. At higher temperatures, ventilation failed to meet rising metabolic demands and anoxic regions expanded rapidly. Above ~37°C, ciliary coordination collapsed and vortical flows dissipated, shifting transport to a diffusion-limited regime accelerating coral mortality. These results identify ciliary beating as a key regulator of thermal tolerance and early indicator of critical physiological tipping points for reef-building corals in a warming, deoxygenating ocean.
SN - 2375-2548
ER -