Determining optimal incubation temperature for a head-start program: the effect of incubation temperature on hatchling Burnett River snapping turtles (Elseya albagula)
Yvonne A. Eiby A B and David T. Booth AA School of Biological Sciences, The University of Queensland, Brisbane, Qld 4072, Australia.
B Corresponding author. Email: y.eiby@uq.edu.au
Australian Journal of Zoology 59(1) 18-25 https://doi.org/10.1071/ZO10080
Submitted: 17 November 2010 Accepted: 19 May 2011 Published: 22 June 2011
Abstract
This study monitored natural nest temperatures and examined the effect of incubation temperature on hatchling phenotype of the freshwater turtle Elseya albagula to determine the optimal temperature for a potential head-start program. Eggs were incubated at constant temperatures (26°C, 28°C and 30°C) to determine the influence of temperature on incubation period, hatchling morphology, swimming performance and post-hatching growth rate. Hatchlings incubated at 26°C had longer plastrons than hatchlings from 30°C and swam faster, three days after hatching, than did hatchlings incubated at either 28°C or 30°C. Incubation temperature also provided a source of variation in hatchling scute patterns. Clutch of origin influenced hatchling mass and size, growth at 184 days after hatching, and the swimming performance of 3-day and 75-day post-hatch hatchlings. Constant temperatures of 26°C and 28°C produced the highest hatching success and highest-quality hatchlings and are therefore recommended for incubation of eggs in a head-start program. In the field, unshaded nests experienced greater daily fluctuations in temperature and higher temperatures overall compared with shaded nests, such that unshaded nest temperatures approached the upper thermal limit to development.
Additional keyword: hatchling.
References
Armstrong, G., and Booth, D. T. (2005). Dietary ecology of the Australian freshwater turtle (Elseya sp. : Chelonia: Chelidae) in the Burnett River, Queensland. Wildlife Research 32, 349–353.| Dietary ecology of the Australian freshwater turtle (Elseya sp. : Chelonia: Chelidae) in the Burnett River, Queensland.Crossref | GoogleScholarGoogle Scholar |
Ashmore, G. M., and Janzen, F. J. (2003). Phenotypic variation in smooth softshell turtles (Apalone mutica) from eggs incubated in constant versus fluctuating temperatures. Oecologia 134, 182–188.
| 12647158PubMed |
Birchard, G. F. (2004). Effects of incubation temperature. In ‘Reptilian Incubation: Environment, Evolution and Behaviour’. (Ed. D. C. Deeming.) pp. 103–123. (Nottingham University Press: Nottingham.)
Bobyn, M. L., and Brooks, R. J. (1994). Interclutch and interpopulation variation in the effects of incubation conditions on sex, survival and growth of hatchling turtles (Chelydra serpentina). Journal of Zoology 233, 233–257.
Booth, D. T. (1998a). Egg size, clutch size, and reproductive effort of the Australian broad-shelled river turtle, Chelodina expansa. Journal of Herpetology 32, 592–596.
| Egg size, clutch size, and reproductive effort of the Australian broad-shelled river turtle, Chelodina expansa.Crossref | GoogleScholarGoogle Scholar |
Booth, D. T. (1998b). Nest temperature and respiratory gases during natural incubation in the broad-shelled river turtle, Chelodina expansa (Testudinata : Chelidae). Australian Journal of Zoology 46, 183–191.
| Nest temperature and respiratory gases during natural incubation in the broad-shelled river turtle, Chelodina expansa (Testudinata : Chelidae).Crossref | GoogleScholarGoogle Scholar |
Booth, D. T. (1999). Incubation temperature and growth of Brisbane river turtle (Emydura signata) hatchlings. Proceedings of the Linnean Society of New South Wales 121, 45–52.
Booth, D. T. (2002). The breaking of diapause in embryonic broad-shell river turtles (Chelodina expansa). Journal of Herpetology 36, 304–307.
Booth, D. T. (2004). Artificial incubation. In ‘Reptilian Incubation: Environment, Evolution and Behaviour’. (Ed. D. C. Deeming.) pp. 253–263. (Nottingham University Press: Nottingham, UK.)
Booth, D. T. (2006). Influence of incubation temperature on hatchling phenotype in reptiles. Physiological and Biochemical Zoology 79, 274–281.
| Influence of incubation temperature on hatchling phenotype in reptiles.Crossref | GoogleScholarGoogle Scholar | 16555187PubMed |
Boulan, R. H. (1999). Reducing threats to eggs and hatchlings: in-situ protection. In ‘Research and Management Techniques for the Conservation of Sea Turtles’. (Eds K. L. Eckert, K. A. Bjorndal, F. A. Abreu-Grobois, and M. Donnelly.) pp. 169–174. IUCN/SSC Marine Turtle Specialist Group Publication No. 4.
Brana, F., and Ji, X. (2000). Influence of incubation temperature on morphology, locomotor performance, and early growth of hatchling wall lizards (Podarcis muralis). The Journal of Experimental Zoology 286, 422–433.
| Influence of incubation temperature on morphology, locomotor performance, and early growth of hatchling wall lizards (Podarcis muralis).Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD3c7kvV2iug%3D%3D&md5=db160c3173c53485581213e10bfea5ffCAS | 10684565PubMed |
Brooks, R. J., Bobyn, M. L., Galbraith, D. A., Layfield, J. A., and Nancekivell, E. G. (1991). Maternal and environmental-influences on growth and survival of embryonic and hatchling snapping turtles (Chelydra serpentina). Canadian Journal of Zoology-Revue Canadienne De Zoologie 69, 2667–2676.
| Maternal and environmental-influences on growth and survival of embryonic and hatchling snapping turtles (Chelydra serpentina).Crossref | GoogleScholarGoogle Scholar |
Burgess, E. A., Booth, D. T., and Lanyon, J. M. (2006). Swimming performance of hatchling green turtles is affected by incubation temperature. Coral Reefs 25, 341–349.
| Swimming performance of hatchling green turtles is affected by incubation temperature.Crossref | GoogleScholarGoogle Scholar |
Christens, E., and Bider, J. (1987). Nesting activity and hatching success of the painted turtle (Chrysemys picta marginata) in south-western Quebec. Herpetologica 43, 55–65.
Deeming, D. C. (2004). Post-hatching phenotypic effects of incubation in reptiles. In ‘Reptilian Incubation: Environment, Evolution and Behaviour’. (Ed. D. C. Deeming.) pp. 229–251. (Nottingham University Press: Nottingham.)
Doody, J. S. (1999). A test of the comparative influences of constant and fluctuating incubation temperatures on phenotypes of hatchling turtles. Chelonian Conversation and Biology 3, 529–531.
Du, W. G., and Ji, X. (2003). The effects of incubation thermal environments on the morphology and locomotor performance and early growth of hatchling soft-shelled turtles, Pelodiscus sinensis. Journal of Thermal Biology 28, 279–286.
| The effects of incubation thermal environments on the morphology and locomotor performance and early growth of hatchling soft-shelled turtles, Pelodiscus sinensis.Crossref | GoogleScholarGoogle Scholar |
Eckert, K. L., and Eckert, S. A. (1990). Embryo mortality and hatch success in in situ and translocated leatherback sea turtle Dermochelys coriacea eggs. Biological Conservation 53, 37–46.
Elphick, M. J., and Shine, R. (1998). Long term effects of incubation temperatures on the morphology and locomotor performance of hatchling lizards (Bassiana duperreyi, Scincidae). Biological Journal of the Linnean Society. Linnean Society of London 63, 429–447.
| Long term effects of incubation temperatures on the morphology and locomotor performance of hatchling lizards (Bassiana duperreyi, Scincidae).Crossref | GoogleScholarGoogle Scholar |
Ewert, M. A., and Legler, J. M. (1978). Hormonal induction of oviposition in turtles. Herpetologica 34, 314–318.
Hamann, M., Schauble, C. S., Limpus, D. J., Emerick, S. P., and Limpus, C. J. (2007). Management plan for the conservation of Elseya sp. (Burnett River) in the Burnett River catchment. Queensland Government Environment Protection Agency, Brisbane.
Janzen, F. J. (1993). The influence of incubation-temperature and family on eggs, embryos, and hatchlings of the smooth softshell turtle (Apalone mutica). Physiological Zoology 66, 349–373.
Janzen, F. J. (1995). Experimental evidence for the evolutionary significance of temperature-dependent sex determination. Evolution 49, 864–873.
| Experimental evidence for the evolutionary significance of temperature-dependent sex determination.Crossref | GoogleScholarGoogle Scholar |
Limpus, C. J., Limpus, D. J., and Hamann, M. (2002). Freshwater turtle populations in the area to be flooded by the Walla Weir, Burnett River, Queensland: baseline study. Memoirs of the Queensland Museum 48, 155–168.
Lynn, W. G., and Ullrich, M. C. (1950). Experimental production of shell abnormality in turtles. Copeia 150, 253–261.
| Experimental production of shell abnormality in turtles.Crossref | GoogleScholarGoogle Scholar |
McCosker, J. (2004). The reproductive ecology of the Brisbane River turtle (Emydura macquarri signata) and the long-necked turtle (Chelodina expansa). Ph.D. Thesis, The University of Queensland.
Miller, K., Packard, G. C., and Packard, M. J. (1987). Hydric conditions during incubation influence locomotor performance of hatchling snapping turtles. The Journal of Experimental Biology 127, 401–412.
Mortimer, J. A. (1999). Reducing threats to eggs and hatchlings: hatcheries. In ‘Research and Management Techniques for the Conservation of Sea Turtles’. (Eds K. L. Eckert, K. A. Bjorndal, F. A. Abreu-Grobois, and M. Donnelly.) pp. 175–178. IUCN/SSC Marine Turtle Specialist Group Publication No. 4.
Mortimer, J. A., Ahmad, Z., Kaslan, S., Daud, M. D., Sharma, D., and Aikanathan, S. (1994). Evaluation of the practice of splitting sea turtle egg clutches under hatchery conditions in Malaysia. In ‘Proceedings of the Thirteenth Annual Symposium on Sea Turtle Biology and Conservation, 23–27 February, 1993. Jekyll Island, Georgia, USA’. (Compilers B. A. Shroeder and B. E. Witherington.) pp. 118–120. NOAA Technical Memorandum NMFS-SEFSC-341.
Nelson, N. J., Keall, S. N., Brown, D., and Daugherty, C. H. (2002). Establishing a new wild population of tuatara (Sphenodon guntheri). Conservation Biology 16, 887–894.
| Establishing a new wild population of tuatara (Sphenodon guntheri).Crossref | GoogleScholarGoogle Scholar |
O’Steen, S. (1998). Embryonic temperature influences juvenile temperature choice and growth rate in snapping turtles Chelydra serpentina. The Journal of Experimental Biology 201, 439–449.
| 1:STN:280:DyaK1c7msVeqtw%3D%3D&md5=4148d6b7cb333db11ba1efa8c479155aCAS |
Packard, G. C., Packard, M. J., Miller, K., and Boardman, T. J. (1987). Influence of moisture, temperature, and substrate on snapping turtle eggs and embryos. Ecology 68, 983–993.
| Influence of moisture, temperature, and substrate on snapping turtle eggs and embryos.Crossref | GoogleScholarGoogle Scholar |
Pena, J. C., Rojac, J. R., Galeano, G., and Meza, V. (1996). Embryo mortality and hatch rate of Trachemys scripta (Testudines: Emydidae) eggs artificially developed in a protected natural area. Revista de Biologia Tropical 44, 841–846.
| 9332615PubMed |
Shine, R. (1995). A new hypothesis for the evolution of viviparity in reptiles. American Naturalist 145, 809–823.
| A new hypothesis for the evolution of viviparity in reptiles.Crossref | GoogleScholarGoogle Scholar |
Thompson, M. B. (1985). Functional significance of the opaque white patch in eggs of Emydura macquarii. In ‘Biology of Australasian Frogs and Reptiles’. (Eds G. Grigg, R. Shine and H. Ehmann.) pp. 387–395. (Royal Zoological Society of New South Wales & Surrey Beatty: Sydney.)
Thomson, S., Georges, A., and Limpus, C. J. (2006). A new species of freshwater turtle in the genus Elseya (Testudines: Chelidae) from central coastal Queensland, Australia. Chelonian Conservation and Biology 5, 74–86.
| A new species of freshwater turtle in the genus Elseya (Testudines: Chelidae) from central coastal Queensland, Australia.Crossref | GoogleScholarGoogle Scholar |
Webb, J. K., Brown, G. P., and Shine, R. (2001). Body size, locomotor speed and antipredator behaviour in a tropical snake (Tropidonophis mairii, Colubridae): the influence of incubation environments and genetic factors. Functional Ecology 15, 561–568.
| Body size, locomotor speed and antipredator behaviour in a tropical snake (Tropidonophis mairii, Colubridae): the influence of incubation environments and genetic factors.Crossref | GoogleScholarGoogle Scholar |