Literature DB >> 31871116

Frogs seek hypoxic microhabitats that accentuate metabolic depression during dormancy.

Giulia S Rossi1, Rebecca L Cramp2, Patricia A Wright3, Craig E Franklin2.   

Abstract

Many animals occupy microhabitats during dormancy where they may encounter hypoxic conditions (e.g. subterranean burrows). We used the green-striped burrowing frog (Cyclorana alboguttata) to test the hypothesis that animals seek hypoxic microhabitats that accentuate metabolic depression during dormancy. We first measured the partial pressure of oxygen (P O2 ) within artificial cavities excavated in wet clay soil, which simulated C. alboguttata underground aestivation chambers, and recorded hypoxic conditions (P O2  as low as 8.9 kPa). Using custom-built tunnels that maintained a longitudinal P O2  gradient (hypoxic to normoxic), we then examined the P O2  preference of C. alboguttata in response to drying habitat conditions. In support of our hypothesis, we found that C. alboguttata chose to spend a greater proportion of time at the hypoxic end of the P O2  gradient compared with the normoxic end. To determine whether hypoxia accentuates metabolic depression in C. alboguttata, we exposed frogs to normoxia (21.0 kPa) or hypoxia (10.5 kPa) for 7 weeks during the transition from an active to an aestivating state. We found that hypoxia exposure accelerated the onset of metabolic depression in C. alboguttata by 2 weeks. Furthermore, we found that frogs exposed to hypoxia exhibited a 66% reduction in O2 consumption after 7 weeks compared with active frogs in normoxia, whereas frogs exposed to normoxia reduced O2 consumption by only 51%. Overall, our findings indicate that some animals may seek microhabitats to maximally depress metabolic rate during dormancy, and that microhabitat O2 availability can have significant implications for energy metabolism.
© 2020. Published by The Company of Biologists Ltd.

Entities:  

Keywords:  Aestivation; Amphibians; Dormancy; Hypometabolism; Hypoxia; Oxygen gradient

Year:  2020        PMID: 31871116     DOI: 10.1242/jeb.218743

Source DB:  PubMed          Journal:  J Exp Biol        ISSN: 0022-0949            Impact factor:   3.312


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