Transplanting gravid lizards to high elevation alters maternal and embryonic oxygen physiology, but not reproductive success or hatchling phenotype

Author:

Kouyoumdjian Laura1ORCID,Gangloff Eric J.1ORCID,Souchet Jérémie1ORCID,Cordero Gerardo A.2ORCID,Dupoué Andréaz3,Aubret Fabien14ORCID

Affiliation:

1. Station d'Ecologie Théorique et Expérimentale du CNRS – UMR 5321, Moulis, France

2. Fachbereich Geowissenschaften, Eberhard Karls Universität Tübingen, Tübingen, Germany

3. CNRS UPMC, UMR 7618, iEES Paris, Université Pierre et Marie Curie, Paris, France

4. School of Molecular and Life Sciences, Curtin University, 6102 WA, Australia

Abstract

Increased global temperatures have opened previously inhospitable habitats, such as at higher elevations. However, the reduction of oxygen partial pressure with increase in elevation represents an important physiological constraint that may limit colonization of such habitats, even if the thermal niche is appropriate. To test the mechanisms underlying the response to ecologically-relevant levels of hypoxia, we performed a translocation experiment with the common wall lizard (Podarcis muralis), a widespread European lizard amenable to establishing populations outside its natural range. We investigated the impacts of hypoxia on the oxygen physiology and reproductive output of gravid common wall lizards and the subsequent development and morphology of their offspring. Lowland females transplanted to high elevations increased their haematocrit and haemoglobin concentration within days and maintained routine metabolism compared to lizards kept at native elevations. However, transplanted lizards suffered from increased reactive oxygen metabolite production near the oviposition date, suggesting a cost of reproduction at high elevation. Transplanted females and females native to different elevations did not differ in reproductive output (clutch size, egg mass, relative clutch mass, or embryonic stage at oviposition) or in post-oviposition body condition. Developing embryos reduced heart rates and prolonged incubation times at high elevations within the native range and at extreme high elevations beyond the current range, but this reduced oxygen availability did not affect metabolic rate, hatching success, or hatchling size. These results suggest that this opportunistic colonizer is capable of successfully responding to novel environmental constraints in these important life-history stages.

Funder

Laboratoire d'Excellence (LabEx) TULIP

Interreg POCTEFA ECTOPYR

European Union

Company of Biologists

Publisher

The Company of Biologists

Subject

Insect Science,Molecular Biology,Animal Science and Zoology,Aquatic Science,Physiology,Ecology, Evolution, Behavior and Systematics

Reference141 articles.

1. Thermal, hydric and respiratory climate of nests;Ackerman,2004

2. Low oxygen: a constraint on the evolution of viviparity in reptiles;Andrews;Physiol. Biochem. Zool.,2002

3. Patterns of embryonic development;Andrews,2004

4. Metabolism of squamate reptiles: allometric and ecological relationships;Andrews;Physiol. Zool.,1985

5. The metabolic cost of reproduction in an oviparous lizard;Angilletta;Funct. Ecol.,2000

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