ArticleScientific reports2020
Vocal panting: a novel thermoregulatory mechanism for enhancing heat tolerance in a desert-adapted bird.
Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 31 citations in OpenAlex.
- Prenatal acoustic communication triggers adaptive vascular programming in the developing avian brain.The Journal of experimental biology · 2026Article
- Thermal Mitigation Behaviors of Captive Blue Peafowls and Visitors' Outdoor Thermal Comfort: A Case Study at Jinan Zoo, China.Animals : an open access journal from MDPI · 2025Article
- A prenatal acoustic signal of heat reduces a biomarker of chronic stress at adulthood across seasons.Frontiers in physiology · 2024Article
- Neurobiology and Changing Ecosystems: Mechanisms Underlying Responses to Human-Generated Environmental Impacts.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023Article
- Thermal acclimatisation to heatwave conditions is rapid but sex-specific in wild zebra finches.Scientific reports · 2023Article
- A prenatal acoustic signal of heat affects thermoregulation capacities at adulthood in an arid-adapted bird.Scientific reports · 2022Article
- Prenatal acoustic programming of mitochondrial function for high temperatures in an arid-adapted bird.Proceedings. Biological sciences · 2021Article
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Authors and funding
4 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Animals thriving in hot deserts rely on extraordinary adaptations and thermoregulatory capacities to cope with heat. Uncovering such adaptations, and how they may be favoured by selection, is essential for predicting climate change impacts. Recently, the arid-adapted zebra finch was discovered to program their offspring's development for heat, by producing 'heat-calls' during incubation in hot conditions. Intriguingly, heat-calls always occur during panting; and, strikingly, avian evaporative cooling mechanisms typically involve vibrating an element of the respiratory tract, which could conceivably produce sound. Therefore, we tested whether heat-call emission results from a particular thermoregulatory mechanism increasing the parent's heat tolerance. We repeatedly measured resting metabolic rate, evaporative water loss (EWL) and heat tolerance in adult wild-derived captive zebra finches (n = 44) at increasing air temperatures up to 44 °C. We found high within-individual repeatability in thermoregulatory patterns, with heat-calling triggered at an individual-specific stage of panting. As expected for thermoregulatory mechanisms, both silent panting and heat-calling significantly increased EWL. However, only heat-calling resulted in greater heat tolerance, demonstrating that "vocal panting" brings a thermoregulatory benefit to the emitter. Our findings therefore not only improve our understanding of the evolution of passerine thermal adaptations, but also highlight a novel evolutionary precursor for acoustic signals.
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