Longevity and larval development among southern bell frogs (Litoria raniformis) in the Coleambally Irrigation Area – implications for conservation of an endangered frog
Reinier M. Mann A D , Ross V. Hyne B , Paulina Selvakumaraswamy C and Sergio S. Barbosa CA Centre for Ecotoxicology (CET), Department of Environmental Sciences, University of Technology-Sydney, PO Box 123, Broadway, NSW 2007, Australia.
B Centre for Ecotoxicology, Ecotoxicology and Environmental Contaminants Section, Department of Environment, Climate Change and Water, PO Box 29, Lidcombe, NSW 1825, Australia.
C Anatomy and Histology, School of Medical Sciences, University of Sydney, NSW 2006, Australia.
D Corresponding author. Email: reinier.mann@uts.edu.au
Wildlife Research 37(6) 447-455 https://doi.org/10.1071/WR10061
Submitted: 1 April 2010 Accepted: 5 August 2010 Published: 18 October 2010
Abstract
Context. With the flow of many of the world’s rivers regulated such that water can be diverted for agriculture and human consumption, basic ecological information on the current status of key biota in significant floodplain wetlands and their response following inundation is needed. The maintenance of natural habitat to ensure amphibian survival is gaining increasing recognition, given the ongoing decline of anuran populations. Information on longevity, time required to emerge from the water and to reach sexual maturity, all provide important information about the required timing, frequency and duration of environmental water allocations to ensure successful recruitment among populations of southern bell frogs (Litoria raniformis Keferstein, 1867).
Aims. The aims of this research were to establish the longevity of southern bell frogs in the Coleambally Irrigation Area (CIA) in the Riverina region of New South Wales, Australia, and to evaluate the capacity for southern bell frog tadpoles to survive and successfully metamorphose following an extended overwintering period.
Methods. Skeletochronology studies were carried out using toe-clips taken from adult and juvenile frogs captured in irrigation channels and rice fields over two rice-growing seasons. For the metamorphosis assay, southern bell frog tadpoles were held back in their development by low temperatures and low food allocation for 290 days, before temperatures and food allocation were increased adequately to allow metamorphosis to occur.
Key results. The study indicated that skeletochronological examination of toe-bones was a useful technique for establishing the age structure of southern bell frogs in this region. The oldest animals in the population were found to be 4–5 years old, although the majority of frogs were typically 2–3 years old. Also, the metamorphosis assay indicated that successful metamorphosis was the exception rather than the rule if tadpole development was held back by low food ration and low temperatures.
Conclusions. If southern bell frogs reach sexual maturity only after 2 years, and the oldest animals observed in the field are 4 or 5 years old, then there is a very narrow window of opportunity – two to three seasons – for each individual to successfully breed.
Implications. The implications for environmental flow management are that habitats for key species identified for protection such as the endangered southern bell frog will need water every 1–2 years to enable each cohort to breed and maintain the wild populations. The extent of the environmental flows needs to be adequate to ensure that water persists long enough for critical biological events such as anuran metamorphosis to occur during the spring and summer months.
Acknowledgements
We gratefully acknowledge Catherine Choung for field assistance and for supplying a subset of the tadpole metamorphosis data. We thank Amanda Rose for technical assistance, Maria Byrne for guidance in the histology and two anonymous reviewers of the manuscript. M. Robb and A. Tiwari (Coleambally Irrigation Cooperative Ltd) are also thanked for liaising with farmers for access to their properties. The authors also appreciate the interest of the participating farmers. Adult L. raniformis were collected and/or maintained under Permit S11480, issued by the NSW National Parks and Wildlife Service. All sampling procedures described here were conducted within the auspices of the Department of Environment, Climate Change & Water (DECCW) Animal Care and Ethics Animal Research Authority Project Approvals 070618/04 and 080331/05. We thank Dr Karrie Rose of the Taronga Wildlife Hospital for undertaking the pathology examinations of L. raniformis frogs that either died in captivity or were killed during this and other projects. We also thank Ashlie Hartigan and Jan Slapeta of the Faculty of Veterinary Science, Sydney University, for information regarding parasite infections. Funding for this project was provided by the Australian Government’s Water for the Future program and the NSW Government’s Rivers Environmental Restoration Program.
Berger, L. , Speare, R. , Hines, H. B. , Marantelli, G. , Hyatt, A. D. , McDonald, K. R. , Skerratt, L. F. , Olsen, V. , Clarke, J. M. , Gillespie, G. , Mahony, M. , Sheppard, N. , Williams, C. , and Tyler, M. J. (2004). Effect of season and temperature on mortality in amphibians due to chytridiomycosis. Australian Veterinary Journal 82, 434–439.
| Crossref | GoogleScholarGoogle Scholar | CAS | CAS | PubMed | PubMed |
Delvinquier, B. L. J. (1986). Myxidium immersum (Protozoa, Myxosporea) of the cane toad, Bufo marinus, in Australian anura, with a synopsis of the genus in amphibians. Australian Journal of Zoology 34, 843–853.
| Crossref | GoogleScholarGoogle Scholar |
Driscoll, D. A. (1999). Skeletochronological assessment of age structure and population stability for two threatened frog species. Australian Journal of Ecology 24, 182–189.
| Crossref | GoogleScholarGoogle Scholar |
Hyne, R. V. , Spolyarich, N. , Wilson, S. P. , Patra, R. W. , Byrne, M. , Gordon, G. , Sánchez-Bayo, F. , and Palmer, C. G. (2009). Distribution of frogs in rice bays within an irrigated agricultural area: links to pesticide usage and farm practice. Environmental Toxicology and Chemistry 28, 1255–1265.
| Crossref | GoogleScholarGoogle Scholar | CAS | CAS | PubMed | PubMed |
Stuart, S. N. , Chanson, J. S. , Cox, N. A. , Young, B. E. , Rodrigues, A. S. L. , Fischman, D. L. , and Waller, R. W. (2004). Status and trends of amphibian declines and extinctions worldwide. Science 306, 1783–1786.
| Crossref | GoogleScholarGoogle Scholar | CAS | CAS | PubMed | PubMed |
Wassens, S. (2008). Review of the past distribution and decline of the southern bell frog Litoria raniformis in New South Wales. Australian Zoologist 34, 446–452.
Wassens, S. , Watts, R. J. , Jansen, A. , and Roshier, D. (2008). Movement patterns of southern bell frog (Litoria raniformis) in response to flooding. Wildlife Research 35, 50–58.
| Crossref | GoogleScholarGoogle Scholar |
Woodhams, D. C. , Alford, R. A. , and Marantelli, G. (2003). Emerging disease of amphibians cured by elevated body temperature. Diseases of Aquatic Organisms 55, 65–67.
| Crossref | GoogleScholarGoogle Scholar | PubMed | PubMed |