Effects of the egg incubation environment on turtle carapace development
- PMID: 36373204
- DOI: 10.1111/ede.12425
Effects of the egg incubation environment on turtle carapace development
Erratum in
-
Erratum.Evol Dev. 2023 May;25(3):253. doi: 10.1111/ede.12435. Epub 2023 Apr 3. Evol Dev. 2023. PMID: 37010003 No abstract available.
Abstract
Developing organisms are often exposed to fluctuating environments that destabilize tissue-scale processes and induce abnormal phenotypes. This might be common in species that lay eggs in the external environment and with little parental care, such as many reptiles. In turtles, morphological development has provided striking examples of abnormal phenotypic patterns, though the influence of the environment remains unclear. To this end, we compared fluctuating asymmetry, as a proxy for developmental instability, in turtle hatchlings incubated in controlled laboratory and unstable natural conditions. Wild and laboratory hatchlings featured similar proportions of supernumerary scales (scutes) on the dorsal shell (carapace). Such abnormal scutes likely elevated shape asymmetry, which was highest in natural nests. Moreover, we tested the hypothesis that hot and dry environments cause abnormal scute formation by subjecting eggs to a range of hydric and thermal laboratory incubation regimes. Shape asymmetry was similar in hatchlings incubated at five constant temperatures (26-30°C). A hot (30°C) and severely Dry substrate yielded smaller hatchlings but scutes were not overtly affected. Our study suggests that changing nest environments contribute to fluctuating asymmetry in egg-laying reptiles, while clarifying the conditions at which turtle shell development remains buffered from the external environment.
Keywords: developmental instability; developmental noise; fluctuating asymmetry; turtle shell development.
© 2022 The Authors. Evolution & Development published by Wiley Periodicals LLC.
References
REFERENCES
-
- Ackerman, R., & Lott, D. (2004). Thermal, hydric and respiratory climate of nest. In D. Deeming (Ed.), Reptilian Incubation: Environment, Evolution and Behaviour (pp. 229-251). Nottingham University Press.
-
- Baken, E. K., Collyer, M. L., Kaliontzopoulou, A., & Adams, D. C. (2021). geomorph v4.0 and gmShiny: Enhanced analytics and a new graphical interface for a comprehensive morphometric experience. Methods in Ecology and Evolution, 12(12), 2355-2363. https://doi.org/10.1111/2041-210x.13723
-
- Bates, D., Mächler, M., Bolker, B., & Walker, S. (2015). Fitting linear mixed-effects models using lme4. Journal of Statistical Software, 67(1), 1-48.
-
- Bentley, B. P., McGlashan, J. K., Bresette, M. J., & Wyneken, J. (2020). No evidence of selection against anomalous scute arrangements between juvenile and adult sea turtles in Florida. Journal of Morphology, 282, 173-184. https://doi.org/10.1002/jmor.21294
-
- Bodensteiner, B. L., Mitchell, T. S., Strickland, J. T., & Janzen, F. J. (2015). Hydric conditions during incubation influence phenotypes of neonatal reptiles in the field. Functional Ecology, 29(5), 710-717. https://doi.org/10.1111/1365-2435.12382
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
