Biomechanics of burst swimming speed in prey and predatory tadpole species
DOI:
https://doi.org/10.11606/issn.2316-9079.v25i1p43-50Keywords:
Antipredator behavior, Anuran larvae, Burst swimming speed, Ephemeral ponds, Foraging habits, Swimming movementsAbstract
Burst swimming speed of tadpoles of seven species of anurans near the city of Dharwad in southern India were studied. During the rainy season most temporary ponds harbor both prey (e.g., planktivorous and herbivorous) and predatory (e.g., omnivorous and carnivorous) tadpoles. Each tadpole species is variable in size, shape, and development. Each has its unique swimming speed, depending on its requirements. Swimming speed in tadpoles is generally used to escape aquatic predators, navigate, and forage for food. Burst swimming speed (Vmax) of the seven sympatric tadpole species belonging to four families were studied in the laboratory. Among these seven species both prey and predatory forms occurred, including Microhyla ornata (planktivorous), Duttaphrynus melanostictus, Uperodon taprobanicus, Sphaerotheca breviceps, Polypedates maculatus (herbivorous), Euphlyctis cyanophlyctis (omnivorous), and Hoplobatrachus tigerinus (carnivorous). Burst swimming speed was recorded for each species in developmental stages 29–30. Swimming speed differed significantly among species. Tadpoles of the carnivorous H. tigerinus exhibited the greatest Vmax (60.21 cm/s), followed by omnivorous E. cyanophlyctis (37.90 cm/s). Herbivorous tadpoles, including P. maculatus (29.27 cm/s), S. breviceps (27.26 cm/s), U. taprobanicus (24.89 cm/s), D. melanostictus (13.58 cm/s) had lower burst speeds, while the planktivorous M. ornata (12.11 cm/s) had the lowest speed. The results of this study show that predatory tadpoles (i.e., carnivorous or omnivorous) had greater swimming speeds than prey tadpoles. Even though prey tadpoles had lower burst swimming speeds than predatory tadpoles, they are still able to avoid predators. Prey tadpoles may have a variety of antipredator mechanisms, including the use of refugia, reduction of swimming movements, prolonged immobility, and cryptic coloration. In conclusion, predatory tadpoles exhibit higher burst swimming speeds than prey tadpoles. This ability facilitates prey capture because their larger size allows them to generate more force.
Downloads
References
Arendt, J. D. 2003. Reduced burst speed is a cost of rapid growth in anuran tadpoles: problems of autocorrelation and inferences about growth rates. Functional Ecology 17: 328–334.
Arendt, J. D. 2009. Influence of sprint speed and body size on predator avoidance in New Mexican spadefoot toads (Spea multiplicata). Oecologia 159: 455–461.
Arendt, J. D. 2010. Morphological correlates of sprint swimming speed in five species of Spadefoot toad tadpoles: comparison of morphometric methods. Journal of Morphology 271: 1044–1052.
Benard, M. F. 2004. Predator-induced phenotypic plasticity in organisms with complex life histories. Annual Review of Ecology, Evolution and Systematics 35: 651–673.
Cano-Barbacil, C., J. Radinger, M. Argudo, F. Rubio-Gracia, A. Vila-Gispert, and E. Garcia-Berthou. 2020. Key factors explaining critical swimming speed in freshwater fish: a review and statistical analysis for Iberian species. Scientific Reports 10: 18947.
Dayton, G. H., D. Saenz, K. A. Baum, R. B. Langerhans, and T. J. DeWitt. 2005. Body shape, burst speed and escape behavior of larval anurans. Oikos 111: 582–591.
Espanha, J., M. F. Vasconcelos, and P. C. Eterovick. 2016. The role of tadpole coloration against visually oriented predators. Behavioral Ecology and Sociobiology 70: 255–267.
Ferrari, M. C. O., B. D. Wisenden, and D. P. Chivers. 2010. Chemical ecology of predator-prey interactions in aquatic ecosystems: a review and prospectus. Canadian Journal of Zoology 88: 698–724.
Gosner, K. L. 1960. A simplified table for staging anuran embryos and larvae with notes on identification. Herpetologica 16: 183–190.
Hews, D. K. 1988. Alarm response in larval western toads, Bufo boreas: release of larval chemicals by a natural predator and its effect on predator capture efficiency. Animal Behaviour 36: 125–133.
Hiragond, N. C. and S. K. Saidapur. 2001. Microhabitat choice of tadpoles of seven anuran species. Current Herpetology 20: 51–60.
Huey, R. B. 1980. Sprint velocity of tadpoles (Bufo boreas) through metamorphosis. Copeia 1980: 537–540.
Lardner, B. 2000. Morphological and life history responses to predators in larvae of seven anurans. Oikos 88: 169–180.
Lima, S. L. and L. M. Dill. 1990. Behavioral decisions made under the risk of predation: a review and prospectus. Canadian Journal of Zoology 68: 619–640.
Liu, H., R. J. Wassersug, and K. Kawachi. 1996. A computational fluid dynamics study of tadpole swimming. Journal of Experimental Biology 199: 1245–1260.
Liu, H., R. J. Wassersug, and K. Kawachi. 1997. The three dimensional hydrodynamics of tadpole locomotion. Journal of Experimental Biology 200: 2807–2819.
Mogali, S. M., S. K. Saidapur, and B. A. Shanbhag. 2011a. Levels of predation modulate antipredator defense behavior and metamorphic traits in the toad Bufo melanostictus. Journal of Herpetology 45: 428–431.
Mogali, S. M., S. K. Saidapur, and B. A. Shanbhag. 2011b. Receding water levels hasten metamorphosis in the frog, Sphaerotheca breviceps (Schneider, 1799): a laboratory study. Current Science 101: 1219–1222.
Mogali, S. M., S. K. Saidapur, and B. A. Shanbhag. 2017. Influence of desiccation threat on the metamorphic traits of the Asian common toad, Duttaphrynus melanostictus (Anura). Acta Herpetologica 12: 175–180.
Mogali, S. M., B. A. Shanbhag, and S. K. Saidapur. 2020. Adaptive significance of the transparent body in the tadpoles of ornamented pygmy frog, Microhyla ornata (Anura, Amphibia). Acta Herpetologica 15: 55–57.
Mogali, S. M., B. A. Shanbhag, and S. K. Saidapur. 2022a. Knowledge of predators and accessibility to refuge reduces larval mortality of the Bicolored frog, Clinotarsus curtipes (Anura: Ranidae). Salamandra 58: 157–160.
Mogali, S. M., B. A. Shanbhag, and S. K. Saidapur. 2022b. Antipredator responses of tadpoles to kairomones from an omnivorous tadpole. Herpetological Review 53 :404–407.
Mogali, S. M., B. A. Shanbhag, and S. K. Saidapur. 2023a. Relative susceptibility of tadpoles of Uperdon taprobanicus (Anura: Microhylidae) and Duttaphrynus melanostictus (Anura: Bufonidae) to predacious Hoplobatrachus tigerinus (Anura: Dicroglossidae) tadpoles: significance of refugia and swimming speed in predator avoidance. Phyllomedusa 22: 139–146.
Mogali, S. M., B. A. Shanbhag, and S. K. Saidapur. 2023b. Antipredator responses of Polypedates maculatus tadpoles to kairomones from the carnivorous tadpoles of Hoplobatrachus tigerinus. Salamandra 59: 83–86.
Mogali, S. M., B. A. Shanbhag, and S. K. Saidapur. 2024. Behavioural responses of predator-naïve, predator-experienced and wild-caught Sphaerotheca breviceps tadpoles to kairomones from the carnivorous tadpoles of Hoplobatrachus tigerinus. Salamandra 60: 147–152.
Nomura, F., V. H. M. Prado, F. R. Silva, R. E. Borges, N. Y. N. Dias, and D. C. Rossa-Feres. 2011. Are you experienced? Predator type and predator experience trade-offs in relation to tadpole mortality rates. Journal of Zoology 284: 144–150.
Richardson, J. M. L. 2002. Burst swimming speed in tadpoles inhabiting ponds with different top predators. Evolutionary Ecology Research 4: 627–642.
Saidapur, S. K. 2001. Behavioral ecology of anuran tadpoles: the Indian scenario. Proceedings of Indian National Science Academy B 67: 311–322.
Saidapur, S. K. 2025. Behavioural ecology and developmental plasticity in Indian anuran tadpoles. Behavioural Ecology and Sociobiology 79: e46.
Schmidt, B. R. and A. Amézquita. 2001. Predator-induced behavioral responses: tadpoles of the neotropical frog Phyllomedusa tarsius do not respond to all predators. Herpetological Journal 11: 9–15.
Spieler, M. and K. E. Linsenmair. 1999. Aggregation behaviour of Bufo maculates tadpoles as an antipredator mechanism. Ethology 105: 665–686.
Van Buskirk, J. V. and A. McCollum. 2000. Influence of tail shape on tadpole swimming performance. Journal of Experimental Biology 203: 2449–2458.
Wassersug, R. J. 1989. Locomotion in amphibian larvae (or ‘Why aren’t tadpoles built like fishes?). American Zoologist 29: 65–84.
Webb, P. W. 1984. Body form, locomotion and foraging in aquatic vertebrates. American Zoologist 24: 107–120
Downloads
Published
Issue
Section
License
Copyright (c) 2026 ESALQ-USP

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
All material originally published in Phyllomedusa belongs to Escola Superior de Agricultura Luiz de Queiroz - Universidade de São Paulo. All contents are under a license of Creative Commons BY-NC-ND.
Impact Factor (JCR): 0.600
CiteScore: 1.0