Qiucheng LIU,Tongliang WANG,Xiaofei ZHAI and Jichao WANG.Call Characteristics of Two Sympatric and Morphologically Similar Tree Frogs Species, Polypedates megacephalus and Polypedates mutus (Anura: Rhacophoridae), from Hainan, China[J].Asian Herpetological Research(AHR),2018,9(4):240-249.[doi:10.16373/j.cnki.ahr.180025]
Click Copy

Call Characteristics of Two Sympatric and Morphologically Similar Tree Frogs Species, Polypedates megacephalus and Polypedates mutus (Anura: Rhacophoridae), from Hainan, China
Share To:

Asian Herpetological Research[ISSN:2095-0357/CN:51-1735/Q]

Issue:
2018 VoI.9 No.4
Page:
240-249
Research Field:
Publishing date:
2018-12-25

Info

Title:
Call Characteristics of Two Sympatric and Morphologically Similar Tree Frogs Species, Polypedates megacephalus and Polypedates mutus (Anura: Rhacophoridae), from Hainan, China
Author(s):
Qiucheng LIU Tongliang WANG Xiaofei ZHAI and Jichao WANG*
Ministry of Education Key Laboratory for Tropical Island Ecology, College of Life Sciences, Hainan Normal University, Haikou 571158, China
Keywords:
body size call characteristics Polypedates sexual selection
PACS:
-
DOI:
10.16373/j.cnki.ahr.180025
Abstract:
Anuran calls are usually species-specific and therefore valued as a tool for species identification. Call characteristics are a potential honest signal in sexual selection because they often reflect male body size. Polypedates megacephalus and P. mutus are two sympatric and morphologically similar tree frogs, but it remains unknown whether their calls are associated with body size. In this study, we compared call characteristics of these two species and investigated any potential relationships with body size. We found that P. megacephalus, males produced six call types which consisting of three distinct notes, while P. mutus males produced five types consisting of two types of notes. Dominant frequency, note duration, pulse duration, and call duration exhibited significant interspecific differences. In P. megacephalus, one note exhibited a dominant frequency that was negatively correlated with body mass, snout-vent length, head length, and head width. In P. mutus, the duration of one note type was positively correlated with body mass and head width. These differences in call characteristics may play an important role in interspecific recognition. Additionally, because interspecific acoustic variation reflects body size, calls may be relevant for sexual selection. Taken together, our results confirmed that calls are a valid tool for distinguishing between the two tree-frog species in the field.

References:

Bastos R. P., Signorelli L., Morais A. R., Costa T. B., Lima L. P., Jr J. P. P. 2011. Advertisement calls of three anuran species (Amphibia) from the Cerrado, Central Brazil. S Am J Herpetol, 6: 67–72
Bee M. A., Kozich C. E., Blackwell K. J., Gerhardt H. C. 2010. Individual variation in advertisement calls of territorial male green frogs, Rana clamitans: implications for individual discrimination. Ethology, 107: 65–84
Bee M. A., Perrill S. A., Owen P. C. 1999. Size assessment in simulated territorial encounters between male green frogs (Rana clamitans). Behav Ecol Sociobiol, 45: 177–184
Boersma P., Weenink D. 2017. Praat: doing phonetics by computer [Computer program],Version 5.1.11. Available from: http://www.praat.org/
Christensen-Dalsgaard J., Ludwig T. A., Narins P. M. 2002. Call diversity in an old world treefrog: level dependence and latency of acoustic responses. Bioacoustics, 13: 21–35
Cui J. G., Tang Y. Z., Narins P. M. 2011. Real estate ads in Emei music frog vocalizations: Female preference for calls emanating from burrows. Biol Lett, 8: 337–340
Fang K., Zhang B. W., Brauth S. E., Tang Y. Z., Fang G. Z. 2018. The first call note of the Anhui tree frog (Rhacophorus zhoukaiya) is acoustically suited for enabling individual recognition. Bioacoustics, DOI: 10.1080/09524622.2017.
1422805
Fei L. 1999. Atlas of Amphibians of China. China: Henan Scientific and Technologic Press, Zhengzhou (In Chinese)
Fei L., Hu S. Q., Ye C. Y., Huang Y. Z. 2009. Fauna Sinica, Vol. 2, Amphibia. Science Press, Beijing China (In Chinese)
Fei L., Ye C. Y., Jiang J. P., Xie F., Huang Y. Z. 2005. An Illustrated Key to Chinese Amphibians. Sichuan Science and Technology, Chengdu China (In Chinese)
Fei L., Ye C. Y., Jiang J. P. 2012. Colored Atlas of Chinese Amphibians and Their Distributions. Sichuan Science and Technology Press, Chengdu (In Chinese)
Forlani M. C., Mendes C. V. D. M., Dias I. R. Ruas D. S., Tonini J. F. R., Sá R. O. D. 2013. The advertisement calls and distribution of two sympatric species of Chiasmocleis (Méhely 1904) (Anura, Microhylidae, Gastrophryninae) from the Atlantic Forest. S Am J Herpetol, 8: 46–51
Gerhardt H. C., Huber F. 2002. Acoustic communication in insects and anurans: Common problems and diverse solutions. University of Chicago Press, Chicago
Gerhardt H. C. 1994. The evolution of vocalization in frogs and toads. Annu Rev Ecol S, 25: 293–324
Given M. F. 1987. Vocalization and acoustic interactions of the carpenter frog, Rana virgatipes. Herpetologica, 43: 467?481
Given M. F. 1988. Territoriality and aggressive interactions of male carpenter frogs, Rana virgatipes. Copeia, 1988: 411?421
Hallowell E. 1861. Report upon the Reptilia of the North Pacific Exploring Expedition, under command of Capt. John Rogers, U.S. N. P Acad Nat Sci Phila, 12: 480–510
Heyer W. R., Barrio-Amorós C. L. 2009. The advertisement calls of two sympatric frogs, Leptodactylus lithonaetes (Amphibia: Anura: Leptodactylidae) and Pristimantis vilarsi (Amphibia: Anura: Strabomantidae). P Biol Soc Wash, 122: 282–291
Inger R. F. 1999. Distributions of amphibians in southern Asia and adjacent islands. Pp. 445–482. In Duellman W. E. (Eds.), Patterns of distribution of amphibians: A global perspective. Baltimore: John Hopkins University Press
Jiang J. P., Xie F., Fei L., Ye C. Y., Zheng M. 2002. Mating calls of six forms of pleobatid in Wa Wu Mountain National Forest Park, Sichuan, China (Anura: Pelobatidae). Zool Res, 23: 89–94 (In Chinese)
Kelley D. B. 2004. Vocal communication in frogs. Curr Opin Neurobiol, 14: 751–757
Kuraishi N., Matsui M., Hamidy A., Belabut D. M., Ahmad N., Panha S., Sudin A., Yong H. S., Jiang J. P., Ota H., Thong H. T., Nishikawa K. 2012. Phylogenetic and taxonomic relationships of the Polypedates leucomystax complex (Amphibia). Zool Scr, 42: 54–70
Kuraishi N., Matsui M., Ota H., Chen S. L. 2011. Specific separation of Polypedates braueri (Vogt, 1911) from P. megacephalus (Hallowell, 1861) (Amphibia: Anura: Rhacophoridae). Zootaxa, 2744: 53–61
K?hler J., Jansen M., Rodríguez A., Pjr K., Toledo L. F., Emmrich M., Glaw F., Haddad C. F. B., R?del M. O., Vences M. 2017. The use of bioacoustics in anuran taxonomy: Theory, terminology, methods and recommendations for best practice. Zootaxa, 4251: 1–124
Liao W. B., Lu X. 2011. Proximate mechanisms leading to large male mating advantage in the Andrew’s toad, Bufo andrewsi. Behaviour, 148: 1087–1102
Liu C. C., Нu S. Q., Yang F. H. 1960. Amphibia of Yunnan collected in 1958. Acta Zoologica Sinica, 12: 149–174
Liu Q. C., Zhai X. F., Wang T. L., Wang J. C. 2018. Morphological identification and diversity of Polypedates species (Rhacophoridae, Anura, Amphibia) on Hainan Island. Sichuan Journal of Zoology, 5(37): 490–496 (In Chinese)
Márquez R., Penna M., Marques P., do Amaral J. P. S. 2005. Diverse types of advertisement calls in the frogs Eupsophus calcaratus and E. roseus (Leptodactylidae): A quantitative comparison. Herpetol J, 15(4): 257–263
Martin W. F. 1972. Evolution of vocalization in the genus Bufo. Pp. 279?309. In Blair W. F. (Eds.), Evolution in the Genus Bufo. University of Texas Press, Austin
Matsui M., Seto T., Utsunomiya T. 1986. Acoustic and karyotypic evidence for specific separation of Polypedates megacephalus from P. leucomystax. J Herpetol, 20: 483–489
Morris M. R., Yoon S. L. 1989. A mechanism for female choice for large males in the treefrog Hyla chrysoscelis. Behav Ecol Sociobiol, 25: 65?71
Narins P. M., Feng A. S., Fay R. R., Popper A. N. 2006. Hearing and sound communication in amphibians. Springer Science, New York
Narins P. M., Lewis E. R., McClell B. E. 2000. Hyperextended call note repertoire of the endemic Madagascar treefrog Boophis madagascariensis (Rhacophoridae). The Zoological Society of London, 250: 283–298
Pan S. L., Dang N. X., Wang J. S., Zheng Y. T., Rao D. Q., Li J. T. 2013. Molecular phylogeny supports the validity of Polypedates impresus yang 2008. Asian Herpetol Res, 4: 124–133
Penna M. 2004. Amplification and spectral shifts of vocalizations inside burrows of the frog Eupsophus calcaratus (Leptodactylidae). J Acoust Soc Am, 116: 1254–1260
Pettitt B. A., Bourne G. R., Bee M. A. 2013. Advertisement call variation in the golden rocket frog (Anomaloglossus beebei): Evidence for individual distinctiveness. Ethology, 119: 244–256
Haddad C. F. B., Pombal Jr. J. P., Batistic R. F. 1994. Natural hybridization between diploid and tetraploid species of Leaf-frogs, Genus Phyllomedusa (Amphibia). J Herpetol, 28(4): 425–430
Pr?hl H. 2003. Variation in male calling behaviour and relation to male mating success in the Strawberry poison frog (Dendrobates piimilio). Ethology, 109: 273–290
Rand A. S., Ryan M. 1981. The adaptive significance of a complex vocal repertoire in a neotropical frog. Ethology, 57: 209–214
Rausch A. M., Sztatecsny M., Jehle R., Ringler E., H?dl W. 2014. Male body size and parental relatedness but not nuptial colouration influence paternity success during scramble competition in Rana arvalis. Behaviour, 151: 1869–1884
Pettitt B. A., Bourne G. R., Bee M. A. 2013. Advertisement call variation in the Golden rocket frog (Anomaloglossus beebei): Evidence for individual distinctiveness. Ethology, 119: 244–256
Richardson C., Joly P., Léna J. P., Plénet S., Lengagne T. 2010. The challenge of finding ahighquality male: A treefrog solution based on female assessment of male calls. Behaviour, 147: 1737–1752
Robisson P., Aubin T., Bremond J. C. 2010. Individuality in the voice of the emperor penguin Aptenodytes forsteri: Adaptation to a noisy environment. Ethology, 94: 279–290
Smith M. J., Hunter D. 2005. Temporal and geographic variation in the advertisement call of the Booroolong frog (Litoria booroolongensis: Anura: Hylidae). Ethology, 111: 1103–1115
Wang J. C., Yang C. C., Lin L., Liu H. W. 2014. Wild Vertebrate In Diaoluoshan, Hainan, China. China Forestry Press, Beijing (In Chinese)
Wang J. C., Cui J. G., Shi H. T., Brauth S. E., Tang Y. Z. 2012. Effects of body size and environmental factors on the acoustic structure and temporal rhythm of calls in Rhacophorus dennysi. Asian Herpetol Res, 3:205–212
Wang J. C., Wang T. L., Wang P. P., Cui J. G. 2016. Calls characteristics in round-tongued floating Phrynoglossus martensii. Chinese Journal of Zoology, 51: 214–220 (In Chinese)
Wei L., Zhao L. H., Ma X. H., Fan X. L., Ma X. M., Lin Z. H. 2012. Advertisement call variability in the black-spined toad Bufo melanostictus (Anura: Bufonidae) during the breeding season in Lishui, Zhejiang, China. Asian Herpetol Res, 3: 157–162
Welch A. M., Semlitsch R. D., Gerhardt H. C. 1998. Call duration as an indicator of genetic quality in male gray tree frogs. Science, 280: 1928–1930
Wells K. D. 1978. Territoriality in the green frog (Rana clamitans): Vocalizations and agonistic behaviour. Anim Behav, 26: 1051?1063
Xiong L. C., Matsui M., Jiang J. P., Nishikawa K. 2015. Advertisement calls of two horned frogs, Megophrys kuatunensis and M. huangshanensis, from China (Anura, Megophryidae). Current Herpetology, 34: 51–59
Xu F., Cui J. G., Song J., Brauth S. E., Tang Y. Z. 2011. Male competition strategies change when information concerning female receptivity is available. Behavi Ecol, 23: 307–312
Xu J. X., Xie F., Jiang J. P., Mo Y. M., Zheng Z. H. 2005. The acoustic features of the mating call of 12 anuran species. Chinese Journal of Zoology, 40: 12–19 (In Chinese)
Zhao E. M., Adler K. 1993. Herpetology of China. Oxford, Ohio:Society for the study of amphibians and reptiles in cooperation with Chinese. Society for the Study of Amphibians and Reptiles
Zhu B. C., Wang J. C., Cui J. G., Brauth S. E., Tang Y. Z. 2016a. The spectral structure of vocalizations match hearing sensitivity but imprecisely in Philautus odontotarsus. Bioacoustics, 121–134
Zhu B. C., Wang J. C., Zhao L. H., Sun Z. X., Cui J. G., Brauth S. E., Tang Y. Z. 2016b. Bigger is not always better: females prefer males of mean body size in Philautus odontotarsus. Plos One, 11(2): e0149879
Zhu B. C., Wang J. C., Zhao L. H., Chen Q., Sun Z. X., Yang Y., Brauth S. E., Tang Y. Z., Cui J. G. 2017. Male-male competition and female choice are differentially affected by male call acoustics in the serrate-legged small treefrog, Kurixalus odontotarsus. PeerJ, 5: e3980

Memo

Memo:
-
Last Update: 2018-12-26