Jorge Ayala-Berdon , Kevin I. Medina-Bello , Jorge D. Carballo-Morales , Romeo A. Saldaña-Vázquez , Federico Villalobos
{"title":"Thermal energetics of bats of the family Vespertilionidae: An evolutionary approach","authors":"Jorge Ayala-Berdon , Kevin I. Medina-Bello , Jorge D. Carballo-Morales , Romeo A. Saldaña-Vázquez , Federico Villalobos","doi":"10.1016/j.zool.2025.126271","DOIUrl":null,"url":null,"abstract":"<div><div>Thermal energetics define the way animals spend energy for thermoregulation. In this regard, numerous studies have determined that body mass (<em>M</em><sub><em>b</em></sub>) is the most influential morphological trait affecting the thermal traits in different species of birds and mammals. However, most of the studies have been focused on the basal metabolic rate (<em>BMR</em>), while other thermal traits have been less studied. We addressed this gap by examining thermal variables on bats of the family Vespertilionidae. Using open-flow respirometry, we measured <em>BMR</em>, absolute thermal conductance (<em>C</em>’), lower and upper critical temperatures (<em>T</em><sub><em>LC</em></sub> and <em>T</em><sub><em>UC</em></sub>), and breadth of the thermoneutral zone (<em>TNZ</em><sub><em>b</em></sub>) of 16 bat species ranging in <em>M</em><sub><em>b</em></sub> from ∼ 4.0–21.0 g from central Mexico. We: 1) combined our empirical data with information gathered from the literature and conducted phylogenetic analyses to investigate the relationship between <em>M</em><sub><em>b</em></sub> and thermal traits, 2) tested the relationship between mass independent <em>C</em>’ and mass independent <em>BMR</em> with <em>T</em><sub><em>LC</em></sub> and <em>T</em><sub><em>UC</em></sub> of bats, and the relationship between critical temperatures and <em>TNZ</em><sub><em>b</em></sub>, and 3) mapped the thermal energetic traits along the phylogeny to explore their evolutionary trends. We found a positive relationship between <em>M</em><sub><em>b</em></sub> and <em>BMR</em> and absolute <em>C’</em> but not to <em>T</em><sub><em>LC</em></sub>, <em>T</em><sub><em>UC</em></sub> and <em>TNZ</em><sub><em>b</em></sub> of bats. Mass independent <em>BMR</em> and mass independent <em>C</em>’ were positively related to <em>T</em><sub><em>LC</em></sub> and <em>T</em><sub><em>UC</em></sub>. Finally, <em>T</em><sub><em>LC</em></sub> showed a negative relationship with <em>TNZ</em><sub><em>b</em></sub> while <em>T</em><sub><em>UC</em></sub> exhibited a positive relationship with this thermal trait. The phylogenetic approach indicates that over the evolutionary history, <em>BMR</em> and <em>C´</em> have decreased while <em>T</em><sub><em>LC</em></sub>, <em>T</em><sub><em>UC</em></sub> and <em>TNZ</em><sub><em>b</em></sub> have increased. Our results suggest that: 1) differences in the limits of the <em>TNZ</em> and <em>C’</em> may have helped bats to avoid the constraints on heat dissipation imposed by ambient temperatures, and 2) adaptive changes in <em>M</em><sub><em>b</em></sub> and thermal traits may have influenced the geographical distribution and energy-saving strategies of bats. These findings contribute to an understanding of how small endotherms cope with thermal challenges, shedding light on the physiological and evolutionary mechanisms that shape species’ ecological niches and biogeographic patterns across diverse environments.</div></div>","PeriodicalId":49330,"journal":{"name":"Zoology","volume":"170 ","pages":"Article 126271"},"PeriodicalIF":1.6000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zoology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0944200625000352","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ZOOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Thermal energetics define the way animals spend energy for thermoregulation. In this regard, numerous studies have determined that body mass (Mb) is the most influential morphological trait affecting the thermal traits in different species of birds and mammals. However, most of the studies have been focused on the basal metabolic rate (BMR), while other thermal traits have been less studied. We addressed this gap by examining thermal variables on bats of the family Vespertilionidae. Using open-flow respirometry, we measured BMR, absolute thermal conductance (C’), lower and upper critical temperatures (TLC and TUC), and breadth of the thermoneutral zone (TNZb) of 16 bat species ranging in Mb from ∼ 4.0–21.0 g from central Mexico. We: 1) combined our empirical data with information gathered from the literature and conducted phylogenetic analyses to investigate the relationship between Mb and thermal traits, 2) tested the relationship between mass independent C’ and mass independent BMR with TLC and TUC of bats, and the relationship between critical temperatures and TNZb, and 3) mapped the thermal energetic traits along the phylogeny to explore their evolutionary trends. We found a positive relationship between Mb and BMR and absolute C’ but not to TLC, TUC and TNZb of bats. Mass independent BMR and mass independent C’ were positively related to TLC and TUC. Finally, TLC showed a negative relationship with TNZb while TUC exhibited a positive relationship with this thermal trait. The phylogenetic approach indicates that over the evolutionary history, BMR and C´ have decreased while TLC, TUC and TNZb have increased. Our results suggest that: 1) differences in the limits of the TNZ and C’ may have helped bats to avoid the constraints on heat dissipation imposed by ambient temperatures, and 2) adaptive changes in Mb and thermal traits may have influenced the geographical distribution and energy-saving strategies of bats. These findings contribute to an understanding of how small endotherms cope with thermal challenges, shedding light on the physiological and evolutionary mechanisms that shape species’ ecological niches and biogeographic patterns across diverse environments.
期刊介绍:
Zoology is a journal devoted to experimental and comparative animal science. It presents a common forum for all scientists who take an explicitly organism oriented and integrative approach to the study of animal form, function, development and evolution.
The journal invites papers that take a comparative or experimental approach to behavior and neurobiology, functional morphology, evolution and development, ecological physiology, and cell biology. Due to the increasing realization that animals exist only within a partnership with symbionts, Zoology encourages submissions of papers focused on the analysis of holobionts or metaorganisms as associations of the macroscopic host in synergistic interdependence with numerous microbial and eukaryotic species.
The editors and the editorial board are committed to presenting science at its best. The editorial team is regularly adjusting editorial practice to the ever changing field of animal biology.