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Forest Degradation and Weather Jointly Affect Early-Life Development in a Tropical Understory Bird.

  • Kung'u GN (Corresponding author)
  • , L Cousseau
  • , V Canoine
  • , J Heiskanen
  • , M Githiru
  • , P Njoroge
  • , P Pellikka
  • , Habel JC
  • , L Lens
  • , B Apfelbeck

Publications: Contribution to journal › Article › Peer Reviewed

Abstract

Tropical forest birds face mounting pressures from habitat loss, degradation, and climate warming, yet their combined effects on early-life development remain unclear. Using over a decade of morphological and behavioural observations from Kenya's Taita Hills and 4 years of nestling corticosterone measurements across eight forest patches differing in size and degradation, we examined how forest quality and climate shape nestling condition in the understorey insectivore placid greenbul (Phyllastrephus cabanisi placidus). Nestlings in smaller or more degraded patches showed lower body condition. Provisioning rates did not vary with forest quality, suggesting that poor condition in degraded habitats may result from lower prey quality rather than reduced parental effort. Unexpectedly, corticosterone levels were higher in larger forest patches, and nestlings with elevated corticosterone also showed more advanced wing development, indicating that corticosterone here may reflect developmental stage (readiness to fledge) rather than condition per se. In addition, nestling condition declined in hot weather. Furthermore, although body extremities were shorter in small or degraded patches at low temperatures, in hot weather nestlings developed extremities similar in length to those in larger, less degraded forest patches, consistent with short-term thermoregulatory plasticity. By contrast, in high-canopy areas tarsus growth decreased with increasing temperature, highlighting that multiple developmental mechanisms may operate simultaneously. High canopy cover also buffered body condition under dry weather, whereas nestlings in low-canopy habitats were particularly vulnerable during drought. Our findings demonstrate how forest degradation and climate interact to shape nestling growth, physiology, and potential thermal plasticity. Maintaining intact forest canopies and large forest patches is thus critical for preserving the microclimatic buffering needed to support offspring development in a warming climate. Because multiple, and sometimes opposing, developmental mechanisms may act simultaneously, integrating morphological, behavioural, and physiological indicators provides a powerful multi-metric approach to disentangle how habitat and climate jointly shape early-life development.

Original languageEnglish
Article numbere70771
JournalGlobal Change Biology
Volume32
Issue number3
DOIs
Publication statusPublished - Mar 2026

Funding

This study was funded in whole or in part by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) – 392075127, the Austrian Science Fund (FWF) [10.55776/I6837] awarded to BA and the Research Foundation Flanders (FWO-grant G.0ABI.24N) awarded to LL and LC. For open access purposes, the author has applied a CC BY public copyright license to any author accepted manuscript version arising from this submission. Corticosterone analysis was funded by the German Ornithologist's Society (DOG) and LiDAR data collection by the European Commission DG International Partnerships under DeSIRA programme (FOOD/2020/418-132), PI PP. G.N.K. is a recipient of a DOC Fellowship of the Austrian Academy of Sciences at the University of Salzburg. We are grateful to the placid greenbul project's field assistants: Laurence Chovu, Jack Kiiru, John Maghanga, Handrison Mganga, Adam Mwakulomba, Oliver Mwakio, Musa Makomba, Nathaniel Mkombola, Nathaniel Ndighila, and Peter Kafusi. We also want to thank Dries van de Loock for his efforts concerning field data collection and Caroline Deimel for laboratory work. Kenya Forest Service kindly facilitated access to the forest fragments. This work was approved by the National Commission for Science, Technology, and Innovation of Kenya (NACOSTI/P/20/7374, NACOSTI/P/16/61881/14065, NACOSTI/P/18/61881/18658, NACOSTI/P/19/61881/27686, NACOSTI/P/20/3322, NACOSTI/P/21/8581), the Kenyan Wildlife Service—Biodiversity Research and Monitoring (KWS/BRM/5001), and the Ghent University ethical committee (EC2022-073). Open Access funding provided by Paris Lodron Universitat Salzburg/KEMÖ. This study was funded in whole or in part by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) – 392075127, the Austrian Science Fund (FWF) [ 10.55776/I6837 ] awarded to BA and the Research Foundation Flanders (FWO‐grant G.0ABI.24N) awarded to LL and LC. For open access purposes, the author has applied a CC BY public copyright license to any author accepted manuscript version arising from this submission. Corticosterone analysis was funded by the German Ornithologist's Society (DOG) and LiDAR data collection by the European Commission DG International Partnerships under DeSIRA programme (FOOD/2020/418‐132), PI PP. G.N.K. is a recipient of a DOC Fellowship of the Austrian Academy of Sciences at the University of Salzburg.

Austrian Fields of Science 2012

  • 106026 Ecosystem research
  • 106048 Animal physiology
  • 106047 Animal ecology

Keywords

  • cooperative breeding
  • breeding success
  • habitat degradation
  • microclimate
  • forest insectivores
  • habitat disturbance
  • climate change

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