Evidence map›Paper›PMID 40356272›Full record

ArticleThe Journal of animal ecology2025

Heat limits scale with metabolism in ectothermic animals.

Nicholas L Payne, Jacinta D Kong, Andrew L Jackson, Amanda E Bates, Simon A Morley, James A Smith, Jean-Francois Arnoldi

Abstract read
In one paragraph

Article in The Journal of animal ecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. A universal thermal performance curve arises in biology and ecology.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Nicholas L PayneTrinity College Dublin, Dublin, Ireland.ORCID 0000-0002-5274-471X
Jacinta D KongTrinity College Dublin, Dublin, Ireland.
Andrew L JacksonTrinity College Dublin, Dublin, Ireland.
Amanda E BatesUniversity of Victoria, Victoria, British Columbia, Canada.
Simon A MorleyBritish Antarctic Survey, Cambridge, UK.
James A SmithUniversity of California Santa Cruz, Santa Cruz, California, USA.ORCID 0000-0002-0496-3221
Jean-Francois ArnoldiCentre National de la Recherche Scientifique, Station d'Ecologie Théorique et Expérimentale de Moulis, Moulis, France.

Funding

Irish Research Council IRCLA/2017/186'Laboratoires d'Excellences (LABEX)' TULIP ANR-10-LABX-41Science Foundation Ireland 18/SIRG/5549
6 · The paper itself

Abstract

Ectotherms given time to acclimate to warmer environments, habitats or experimental treatments tend to tolerate higher maximum temperatures, but only slightly higher. This means warmer acclimated organisms live closer to their physiological temperature limits (their 'critical temperatures'). The reason for this modest-and often highly variable-plasticity of heat limits is debated but raises concerns for resilience to future climate warming. Experiments have shown heat tolerance is dependent not just on the magnitude of thermal stress but also on time via exposure duration. This implicates rate processes in the regulation of heat limits, yet few studies have explored this possibility. Invoking biological rates (such as metabolic rate) to explain the plasticity of critical temperatures is complicated by the need to account for temperature, time and the nonlinear dependence of rates on temperature. We developed a new approach to explore whether incorporating estimated metabolic rate and its thermal scaling could explain the apparently modest and highly variable capacities of ectotherms to adjust their heat limits. To do this, we re-evaluate a large thermal tolerance dataset for diverse ectothermic animals heated from different acclimation temperatures up to their critical temperature. By integrating temperature, time and the exponential relationship between temperature and metabolic rate, we compute a cumulative 'metabolic currency' that ectotherms expend (or accumulate) before reaching their heat limits. We then explore how this quantity varies for ectotherms acclimated to different temperatures. Our 'metabolic rescaling' has a dramatic impact on explaining variation in heat limits, revealing that heating tolerance is effectively fixed within a species such that heat limits from any acclimation temperature can be predicted with remarkable accuracy by measuring heat limits at any other acclimation temperature. Heating rate also has a strong, consistent, influence. Evidently, warmer-acclimated organisms only marginally elevate their critical temperatures because they have a fixed amount of energy to spend during heating, and they spend it at a faster rate in warmer temperatures. This provides a very different perspective to leading explanations that organismal heat limits are constrained by hard physiological boundaries and instead encourages unification of thermal tolerance and metabolic scaling theory.

Indexed as

Energy MetabolismHot TemperatureThermotoleranceAcclimatizationAnimalsBasal MetabolismModels, Biologicalacclimationheat tolerancephysiologyscalingthermal limitswarming temperatures

Identifiers

PMID40356272
PMCPMC12134445

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.