Evidence map›Paper›PMID 42744327›Full record

ArticleProceedings. Biological sciences2026

Pervasive sublethal impacts of heat exposure revealed by telomere dynamics.

Justin R Eastwood, Niki Teunissen, Michelle Hall, Sjouke A Kingma, Michael J Roast, Nataly H Aranzamendi, Ian Hoppe, Ariana L Porte, Simon Verhulst, Anne Peters

Abstract read
In one paragraph

Article in Proceedings. Biological sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Justin R EastwoodSchool of Biological Sciences, Monash University , 25 Rainforest Walk, Clayton, Victoria 3800, Australia.ORCID 0000-0002-5294-3321
Niki TeunissenSchool of Biological Sciences, Monash University , 25 Rainforest Walk, Clayton, Victoria 3800, Australia.ORCID 0000-0001-7028-0034
Michelle HallMax Planck Institute for Ornithology , Vogelwarte Radolfzell, Schlossallee 2, 78315 Radolfzell, Germany.
Sjouke A KingmaBush Heritage Australia , 395 Collins Street, Melbourne, Vic 3000, Australia.
Michael J RoastSchool of Biological Sciences, Monash University , 25 Rainforest Walk, Clayton, Victoria 3800, Australia.ORCID 0000-0002-9454-7562
Nataly H AranzamendiSchool of Agriculture and Environment, University of Western Australia , Crawley, WA 6009, Australia.ORCID 0000-0001-6967-0780
Ian HoppeKonrad Lorenz Institute of Ethology (KLIVV), University of Veterinary Medicine Vienna , 1a Savoyenstrasse, 1160 Vienna, Austria.
Ariana L PorteKonrad Lorenz Institute of Ethology (KLIVV), University of Veterinary Medicine Vienna , 1a Savoyenstrasse, 1160 Vienna, Austria.
Simon VerhulstGroningen Institute for Evolutionary Life Sciences, University of Groningen , Nijenborgh 7, 9747 AG Groningen, The Netherlands.ORCID 0000-0002-1143-6868
Anne PetersSchool of Biological Sciences, Monash University , 25 Rainforest Walk, Clayton, Victoria 3800, Australia.ORCID 0000-0001-8071-0560

Funding

Australian Research Council DP150103595Australian Research Council DP180100058Australian Research Council DP210100328Australian Research Council DP240100330Australian Research Council FT110100505Max Planck Society Minerva Program
6 · The paper itself

Abstract

Predicting species responses to anthropogenic environmental change remains one of the most pressing and complex challenges in contemporary biology. While mass mortality events and localized extinctions have been linked to global warming, the more elusive and probably common, effects of sublethal heat are less well understood. In a cooperatively breeding bird from the Australian tropical savannah, we identified that hotter conditions accelerated telomere attrition through two critical life-history stages: juveniles transitioning to nutritional independence and adults transitioning into a reproductive phase. In both stages, there was no capacity for environmental or social conditions to mitigate heat-related telomere attrition, except in adults inhabiting high-density vegetation. These findings demonstrate that sublethal heat effects can have pervasive cryptic consequences for individual somatic state, thereby reducing fitness. More generally, our findings, although probably widespread and concerning for population persistence, also highlight the importance of preserving climate refugia in conservation strategies amid rising sublethal temperatures.

Indexed as

Hot TemperatureTelomereAnimalsAustraliaGlobal Warmingclimate warmingearly lifefitnesshabitat degradationtelomere length

Identifiers

PMID42744327
PMCPMC13577806

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.