Caves, crevices and cooling capacity: Roost microclimate predicts heat tolerance in bats
The microsites that animals occupy during the rest phase of their circadian activity cycle influence their physiology and behaviour, but relatively few studies have examined correlations between interspecific variation in thermal physiology and roost microclimate. Among bats, there is some evidence...
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Veröffentlicht in: | Functional ecology 2022-01, Vol.36 (1), p.38-50 |
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description | The microsites that animals occupy during the rest phase of their circadian activity cycle influence their physiology and behaviour, but relatively few studies have examined correlations between interspecific variation in thermal physiology and roost microclimate. Among bats, there is some evidence that species exposed to high roost temperatures (Troost) possess greater heat tolerance and evaporative cooling capacity, but the small number of species for which both thermal physiology and roost microclimate data exist mean that the generality of this pattern remains unclear.
Here, we test the hypothesis that bat heat tolerance and evaporative cooling capacity have co‐evolved with roost preferences. We predicted that species occupying roosts poorly buffered from high outside environmental temperature exhibit higher heat tolerance and evaporative cooling capacity compared to species inhabiting buffered roosts in which Troost remains well below outside conditions.
We used flow‐through respirometry to investigate thermoregulation at air temperatures (Ta) approaching and exceeding normothermic body temperature (Tb) among six species with broadly similar body mass but differing in roost microclimate (hot vs. cool roosts). We combined these data with empirical measurements of Troost for each study population.
Hot‐roosting species tolerated Ta ~4°C higher than cool‐roosting bats before the onset of loss of coordinated locomotion and non‐regulated hyperthermia. The evaporative scope (i.e. ratio of maximum evaporative water loss [EWL] to minimum thermoneutral EWL) of hot‐roosting species (16.1 ± 2.4) was substantially higher than that of cool‐roosting species (5.9 ± 2.4). Maximum evaporative cooling capacities (i.e. evaporative heat loss/metabolic heat production) of hot‐roosting species were >2, while the corresponding values for cool‐roosting species were ≤1.
The greater heat tolerance and higher evaporative cooling capacity of hot‐roosting species compared with those occupying cooler roosts reveal variation in bat evaporative cooling capacity correlated with roost microclimate, supporting the hypothesis that thermal physiology has co‐evolved with roost preference.
A free Plain Language Summary can be found within the Supporting Information of this article.
A free Plain Language Summary can be found within the Supporting Information of this article. |
doi_str_mv | 10.1111/1365-2435.13918 |
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Here, we test the hypothesis that bat heat tolerance and evaporative cooling capacity have co‐evolved with roost preferences. We predicted that species occupying roosts poorly buffered from high outside environmental temperature exhibit higher heat tolerance and evaporative cooling capacity compared to species inhabiting buffered roosts in which Troost remains well below outside conditions.
We used flow‐through respirometry to investigate thermoregulation at air temperatures (Ta) approaching and exceeding normothermic body temperature (Tb) among six species with broadly similar body mass but differing in roost microclimate (hot vs. cool roosts). We combined these data with empirical measurements of Troost for each study population.
Hot‐roosting species tolerated Ta ~4°C higher than cool‐roosting bats before the onset of loss of coordinated locomotion and non‐regulated hyperthermia. The evaporative scope (i.e. ratio of maximum evaporative water loss [EWL] to minimum thermoneutral EWL) of hot‐roosting species (16.1 ± 2.4) was substantially higher than that of cool‐roosting species (5.9 ± 2.4). Maximum evaporative cooling capacities (i.e. evaporative heat loss/metabolic heat production) of hot‐roosting species were >2, while the corresponding values for cool‐roosting species were ≤1.
The greater heat tolerance and higher evaporative cooling capacity of hot‐roosting species compared with those occupying cooler roosts reveal variation in bat evaporative cooling capacity correlated with roost microclimate, supporting the hypothesis that thermal physiology has co‐evolved with roost preference.
A free Plain Language Summary can be found within the Supporting Information of this article.
A free Plain Language Summary can be found within the Supporting Information of this article.</description><identifier>ISSN: 0269-8463</identifier><identifier>EISSN: 1365-2435</identifier><identifier>DOI: 10.1111/1365-2435.13918</identifier><language>eng</language><publisher>London: Wiley Subscription Services, Inc</publisher><subject>Air temperature ; bats ; Body mass ; Body temperature ; Buffers ; Caves ; Chiroptera ; Circadian rhythms ; Cooling ; Evaporative cooling ; evaporative water loss ; Heat ; Heat loss ; Heat tolerance ; Hyperthermia ; Hypotheses ; Locomotion ; Microclimate ; Physiology ; Population studies ; Respirometry ; resting metabolic rate ; roost microclimate ; Roosts ; Species ; Temperature tolerance ; Thermoregulation ; Water loss</subject><ispartof>Functional ecology, 2022-01, Vol.36 (1), p.38-50</ispartof><rights>2021 British Ecological Society</rights><rights>2022 British Ecological Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3158-e6fd187bc09f0b0862730ff0393c71a6ed1390e74140f270b0776f10b43cf8953</citedby><cites>FETCH-LOGICAL-c3158-e6fd187bc09f0b0862730ff0393c71a6ed1390e74140f270b0776f10b43cf8953</cites><orcidid>0000-0002-1113-7593 ; 0000-0001-5342-7313 ; 0000-0003-4160-8242 ; 0000-0001-5154-5922 ; 0000-0002-1524-1021</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1365-2435.13918$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1365-2435.13918$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids></links><search><creatorcontrib>Czenze, Zenon J.</creatorcontrib><creatorcontrib>Smit, Ben</creatorcontrib><creatorcontrib>Jaarsveld, Barry</creatorcontrib><creatorcontrib>Freeman, Marc T.</creatorcontrib><creatorcontrib>McKechnie, Andrew E.</creatorcontrib><title>Caves, crevices and cooling capacity: Roost microclimate predicts heat tolerance in bats</title><title>Functional ecology</title><description>The microsites that animals occupy during the rest phase of their circadian activity cycle influence their physiology and behaviour, but relatively few studies have examined correlations between interspecific variation in thermal physiology and roost microclimate. Among bats, there is some evidence that species exposed to high roost temperatures (Troost) possess greater heat tolerance and evaporative cooling capacity, but the small number of species for which both thermal physiology and roost microclimate data exist mean that the generality of this pattern remains unclear.
Here, we test the hypothesis that bat heat tolerance and evaporative cooling capacity have co‐evolved with roost preferences. We predicted that species occupying roosts poorly buffered from high outside environmental temperature exhibit higher heat tolerance and evaporative cooling capacity compared to species inhabiting buffered roosts in which Troost remains well below outside conditions.
We used flow‐through respirometry to investigate thermoregulation at air temperatures (Ta) approaching and exceeding normothermic body temperature (Tb) among six species with broadly similar body mass but differing in roost microclimate (hot vs. cool roosts). We combined these data with empirical measurements of Troost for each study population.
Hot‐roosting species tolerated Ta ~4°C higher than cool‐roosting bats before the onset of loss of coordinated locomotion and non‐regulated hyperthermia. The evaporative scope (i.e. ratio of maximum evaporative water loss [EWL] to minimum thermoneutral EWL) of hot‐roosting species (16.1 ± 2.4) was substantially higher than that of cool‐roosting species (5.9 ± 2.4). Maximum evaporative cooling capacities (i.e. evaporative heat loss/metabolic heat production) of hot‐roosting species were >2, while the corresponding values for cool‐roosting species were ≤1.
The greater heat tolerance and higher evaporative cooling capacity of hot‐roosting species compared with those occupying cooler roosts reveal variation in bat evaporative cooling capacity correlated with roost microclimate, supporting the hypothesis that thermal physiology has co‐evolved with roost preference.
A free Plain Language Summary can be found within the Supporting Information of this article.
A free Plain Language Summary can be found within the Supporting Information of this article.</description><subject>Air temperature</subject><subject>bats</subject><subject>Body mass</subject><subject>Body temperature</subject><subject>Buffers</subject><subject>Caves</subject><subject>Chiroptera</subject><subject>Circadian rhythms</subject><subject>Cooling</subject><subject>Evaporative cooling</subject><subject>evaporative water loss</subject><subject>Heat</subject><subject>Heat loss</subject><subject>Heat tolerance</subject><subject>Hyperthermia</subject><subject>Hypotheses</subject><subject>Locomotion</subject><subject>Microclimate</subject><subject>Physiology</subject><subject>Population studies</subject><subject>Respirometry</subject><subject>resting metabolic rate</subject><subject>roost microclimate</subject><subject>Roosts</subject><subject>Species</subject><subject>Temperature tolerance</subject><subject>Thermoregulation</subject><subject>Water loss</subject><issn>0269-8463</issn><issn>1365-2435</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkMFLwzAUh4MoOKdnrwGvdiZNm7TeZGwqDARR8BbS9EUzuqYm2WT_vZkVr-byIHy_9_h9CF1SMqPp3VDGyywvWDmjrKbVEZr8_RyjCcl5nVUFZ6foLIQ1IaQu83yC3uZqB-Eaaw87qyFg1bdYO9fZ_h1rNSht4_4WPzsXIt5Y7Z3u7EZFwIOH1uoY8AeoiKPrwKteA7Y9blQM5-jEqC7Axe-cotfl4mX-kK2e7h_nd6tMM1pWGXDT0ko0mtSGNKTiuWDEGMJqpgVVHNrUhoAoaEFMLhIiBDeUNAXTpqpLNkVX497Bu88thCjXbuv7dFLmnHJRC0ZZom5GKhUIwYORg081_F5SIg_65EGWPMiSP_pSohwTX7aD_X-4XC7mY-4bkR5wdw</recordid><startdate>202201</startdate><enddate>202201</enddate><creator>Czenze, Zenon J.</creator><creator>Smit, Ben</creator><creator>Jaarsveld, Barry</creator><creator>Freeman, Marc T.</creator><creator>McKechnie, Andrew E.</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><orcidid>https://orcid.org/0000-0002-1113-7593</orcidid><orcidid>https://orcid.org/0000-0001-5342-7313</orcidid><orcidid>https://orcid.org/0000-0003-4160-8242</orcidid><orcidid>https://orcid.org/0000-0001-5154-5922</orcidid><orcidid>https://orcid.org/0000-0002-1524-1021</orcidid></search><sort><creationdate>202201</creationdate><title>Caves, crevices and cooling capacity: Roost microclimate predicts heat tolerance in bats</title><author>Czenze, Zenon J. ; Smit, Ben ; Jaarsveld, Barry ; Freeman, Marc T. ; McKechnie, Andrew E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3158-e6fd187bc09f0b0862730ff0393c71a6ed1390e74140f270b0776f10b43cf8953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Air temperature</topic><topic>bats</topic><topic>Body mass</topic><topic>Body temperature</topic><topic>Buffers</topic><topic>Caves</topic><topic>Chiroptera</topic><topic>Circadian rhythms</topic><topic>Cooling</topic><topic>Evaporative cooling</topic><topic>evaporative water loss</topic><topic>Heat</topic><topic>Heat loss</topic><topic>Heat tolerance</topic><topic>Hyperthermia</topic><topic>Hypotheses</topic><topic>Locomotion</topic><topic>Microclimate</topic><topic>Physiology</topic><topic>Population studies</topic><topic>Respirometry</topic><topic>resting metabolic rate</topic><topic>roost microclimate</topic><topic>Roosts</topic><topic>Species</topic><topic>Temperature tolerance</topic><topic>Thermoregulation</topic><topic>Water loss</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Czenze, Zenon J.</creatorcontrib><creatorcontrib>Smit, Ben</creatorcontrib><creatorcontrib>Jaarsveld, Barry</creatorcontrib><creatorcontrib>Freeman, Marc T.</creatorcontrib><creatorcontrib>McKechnie, Andrew E.</creatorcontrib><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Functional ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Czenze, Zenon J.</au><au>Smit, Ben</au><au>Jaarsveld, Barry</au><au>Freeman, Marc T.</au><au>McKechnie, Andrew E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Caves, crevices and cooling capacity: Roost microclimate predicts heat tolerance in bats</atitle><jtitle>Functional ecology</jtitle><date>2022-01</date><risdate>2022</risdate><volume>36</volume><issue>1</issue><spage>38</spage><epage>50</epage><pages>38-50</pages><issn>0269-8463</issn><eissn>1365-2435</eissn><abstract>The microsites that animals occupy during the rest phase of their circadian activity cycle influence their physiology and behaviour, but relatively few studies have examined correlations between interspecific variation in thermal physiology and roost microclimate. Among bats, there is some evidence that species exposed to high roost temperatures (Troost) possess greater heat tolerance and evaporative cooling capacity, but the small number of species for which both thermal physiology and roost microclimate data exist mean that the generality of this pattern remains unclear.
Here, we test the hypothesis that bat heat tolerance and evaporative cooling capacity have co‐evolved with roost preferences. We predicted that species occupying roosts poorly buffered from high outside environmental temperature exhibit higher heat tolerance and evaporative cooling capacity compared to species inhabiting buffered roosts in which Troost remains well below outside conditions.
We used flow‐through respirometry to investigate thermoregulation at air temperatures (Ta) approaching and exceeding normothermic body temperature (Tb) among six species with broadly similar body mass but differing in roost microclimate (hot vs. cool roosts). We combined these data with empirical measurements of Troost for each study population.
Hot‐roosting species tolerated Ta ~4°C higher than cool‐roosting bats before the onset of loss of coordinated locomotion and non‐regulated hyperthermia. The evaporative scope (i.e. ratio of maximum evaporative water loss [EWL] to minimum thermoneutral EWL) of hot‐roosting species (16.1 ± 2.4) was substantially higher than that of cool‐roosting species (5.9 ± 2.4). Maximum evaporative cooling capacities (i.e. evaporative heat loss/metabolic heat production) of hot‐roosting species were >2, while the corresponding values for cool‐roosting species were ≤1.
The greater heat tolerance and higher evaporative cooling capacity of hot‐roosting species compared with those occupying cooler roosts reveal variation in bat evaporative cooling capacity correlated with roost microclimate, supporting the hypothesis that thermal physiology has co‐evolved with roost preference.
A free Plain Language Summary can be found within the Supporting Information of this article.
A free Plain Language Summary can be found within the Supporting Information of this article.</abstract><cop>London</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/1365-2435.13918</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-1113-7593</orcidid><orcidid>https://orcid.org/0000-0001-5342-7313</orcidid><orcidid>https://orcid.org/0000-0003-4160-8242</orcidid><orcidid>https://orcid.org/0000-0001-5154-5922</orcidid><orcidid>https://orcid.org/0000-0002-1524-1021</orcidid></addata></record> |
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subjects | Air temperature bats Body mass Body temperature Buffers Caves Chiroptera Circadian rhythms Cooling Evaporative cooling evaporative water loss Heat Heat loss Heat tolerance Hyperthermia Hypotheses Locomotion Microclimate Physiology Population studies Respirometry resting metabolic rate roost microclimate Roosts Species Temperature tolerance Thermoregulation Water loss |
title | Caves, crevices and cooling capacity: Roost microclimate predicts heat tolerance in bats |
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