Vol. 19 No. 1 (2024)
Articles

Autecology of the gecko Phyllopezus periosus (Squamata: Phyllodactylidae) inhabiting rock cliffs of a waterfall canyon from the semi-arid region of northeastern Brazil

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  • José Guilherme Gonçalves-Sousa,
  • Herivelto Faustino Oliveira,
  • Robson Waldemar Avila
José Guilherme Gonçalves-Sousa
Laboratório de Biologia e Ecologia de Animais Silvestres, Instituto de Formação de Educadores, Universidade Federal do Cariri, Ceará
Herivelto Faustino Oliveira
Núcleo Regional de Ofiologia, Departamento de Biologia, Universidade Federal do Ceará, Pici campus, Ceará
Robson Waldemar Avila
Núcleo Regional de Ofiologia, Departamento de Biologia, Universidade Federal do Ceará, Pici campus, Ceará
DOI: https://doi.org/10.36253/a_h-15046

Published 2024-06-21

Keywords

  • Caatinga,
  • Daily activity,
  • Diet,
  • Foraging mode,
  • Microhabitat use,
  • Reproduction,
  • Sexual size dimorphism
    • ...More
    Less

How to Cite

Gonçalves-Sousa, J. G., Oliveira, H. F., & Avila, R. W. (2024). Autecology of the gecko Phyllopezus periosus (Squamata: Phyllodactylidae) inhabiting rock cliffs of a waterfall canyon from the semi-arid region of northeastern Brazil. Acta Herpetologica, 19(1), 41–55. https://doi.org/10.36253/a_h-15046

Copyright (c) 2024 José Guilherme Gonçalves-Sousa, Herivelto F Oliveira, Robson W Avila

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This work is licensed under a Creative Commons Attribution 4.0 International License.

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Abstract

Phyllopezus periosus is the largest phyllodactilid in Brazil, with a relictual distribution in the Caatinga Domain. Herein, we investigated the autecology of P. periosus, describing activity patterns, microhabitat use (spatial niche dimension), foraging mode, body temperature, reproduction, diet (trophic niche dimension), and temperature. Also, we tested the influence of seasonality and ontogeny on these biological aspects. Geckos (n = 116, 54 females, 33 males, and 29 juveniles) were sampled from October 2013 to September 2014. Phyllopezus periosus has an unimodal activity pattern, with peak activity in the early hours of the night. Males are more robust than females, and forelimbs in females are longer than in males. The body temperatures of this thermoconformer gecko are higher in the dry season. The reproductive season begins in the early dry season, with a fixed clutch of two eggs. Although we did not find evidence of more than one clutch per year, the studied population of P. periosus reproduces for an extended period throughout the dry season, as highlighted by the presence of juveniles all year. Phyllopezus periosus is saxicolous and presents a generalist diet composed mainly of arthropods, also including vertebrates such as frogs and lizards.

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References

  1. Alcantara, E.P., Ferreira-Silva, C., Goncalves-Sousa, J.G., Morais, D.H., Ávila, R.W. (2019): Feeding ecology, reproductive biology, and parasitism of Gymnodactylus geckoides Spix, 1825 from a Caatinga area in northeastern Brazil. Herpetol. Conserv. Biol. 14: 641-647.
  2. Alcantara, E.P., Ferreira-Silva, C., Sousa, J.G.G., Ávila, R.W., Morais, D.H. (2018): Ecology and parasitism of the lizard Tropidurus jaguaribanus (Squamata: Tropiduridae) from northeastern Brazil. Phyllomedusa: J. Herpetol. 17: 195-210. DOI: https://doi.org/10.11606/issn.2316-9079.v17i2p195-210
  3. Andrade, M.J.M., Sales, R.F.D., Freire, E.M.X. (2013): Ecology and diversity of a lizard community in the semiarid region of Brazil. Biota Neotrop. 13: 199-209. DOI: https://doi.org/10.1590/S1676-06032013000300023
  4. Barden, G., Shine, R. (1994): Effects of sex and reproductive mode on dietary composition of the reproductively bimodal scincid lizard, Lerista bougainvillii. Aust. Zool. 29, 225-228. DOI: https://doi.org/10.7882/AZ.1994.009
  5. Bauer, A.M. (2007): The foraging biology of the Gekkota: life in the middle. In: Lizard ecology: the evolutionary consequences of foraging mode, pp. 371-404. Reilly, S.M., Mcbrayer, L.D., Miles, D.B., Eds, Cambridge University Press, United Kingdom. DOI: https://doi.org/10.1017/CBO9780511752438.014
  6. Bels, V.L., Pallandre, J.-P., Charlier, S., Maillard, A., Legreneur, P., Russell, A.P., Paindavoine, A.-S., Zghikh, L.-N., Paulet, E., Van Gysel, E. (2019): Predatory behavior in lizards: strategies and mechanisms for catching prey. In: Behavior of Lizards: Evolutionary and Mechanistic Perspectives, Vol. 1, pp. 107-141. Bels, V., Russell, A., Eds, CRC Press, USA. DOI: https://doi.org/10.1201/9781498782739-5
  7. Cacciali, P., Lotzkat, S., Gamble, T., Köhler, G. (2018): Cryptic diversity in the Neotropical gecko genus Phyllopezus Peters, 1878 (Reptilia: Squamata: Phyllodactylidae): A new species from Paraguay. Int. J. Zool. 2018: 3958327. DOI: https://doi.org/10.1155/2018/3958327
  8. Castro-Franco, R., Bustos-Zagal, M.G. (2011): Variation in parental investment and relative clutch mass of the spiny-tail iguana, Ctenosaura pectinata (Squamata: Iguanidae) in central México. Rev. Mex. Biodivers. 82: 199-204. DOI: https://doi.org/10.22201/ib.20078706e.2011.1.454
  9. Conselho Federal de Medicina Veterinária (2002): Resolução n° 714, 20 de junho. Procedimentos e métodos de eutanásia em animais. Available at http://portal.cfmv.gov.br/portal/lei/download-arquivo/id/326. Archived by WebCite at http://www.webcitation.org/6znsPN5t5 on 30 May 2018.
  10. Cooper Jr, W.E., Vitt, L.J., Caldwell, J.P., Fox, S.F. (2001): Foraging modes of some American lizards: relationships among measurement variables and discreteness of modes. Herpetologica 57: 65-76.
  11. Cummings, C., Gamble, T., Wells, M. (2021): A comparison of the foraging biology of two tropical gecko species in disturbed areas. S. Am. J. Herpetol. 19: 8-11. DOI: https://doi.org/10.2994/SAJH-D-18-00026.1
  12. Cunningham, E., Birkhead, T. (1998): Sex roles and sexual selection. Anim. Behav. 56: 1311-1321. DOI: https://doi.org/10.1006/anbe.1998.0953
  13. Faria, R.G., Araujo, A.F.B. (2004): Sintopy of two Tropidurus lizard species (Squamata: Tropiduridae) in a rocky cerrado habitat in central Brazil. Braz. J. Biol. 64: 775-786. DOI: https://doi.org/10.1590/S1519-69842004000500007
  14. Ferreira, A.S., Conceição, B.M., França, L.M., Silva, A.O. (2014): Ecologia Térmica, Padrão de Atividade e Uso de Hábitat pelo lagarto noturno, Phyllopezus pollicaris (Phyllodactylidae), em uma área de Caatinga no Nordeste do Brasil. Rev. Nordest. Zool. 8: 52-69.
  15. Fox, J., Weisberg, S. (2019): An R Companion to Applied Regression, Third Edition. Thousand Oaks CA: Sage. Available at https://cran.r-project.org/web/packages/car/index.html (accessed on 26 February 2024).
  16. Franzini, L.D., Silva, I.R.S., Santana, D.O., Delfim, F.R., Vieira, G.H.C., Mesquita, D.O. (2019): Lizards (Lacertilia) from Paraíba state, Northeast, Brazil: current knowledge and sampling discontinuities. Herpetol. Notes 12: 749-763.
  17. Freitas, P.R.S., França, F.G.R., Mesquita, D.O. (2015): Aspectos demográficos dos lagartos Phyllopezus periosus e Phyllopezus pollicaris (Sauria: Phyllodactylidae) em simpatria em área de Caatinga no Nordeste do Brasil. Gaia Sci. 8: 294-305.
  18. Gamble, T., Bauer, A.M., Greenbaum, E., Jackman, T.R. (2008): Out of the blue: a novel, trans‐Atlantic clade of geckos (Gekkota, Squamata). Zool. Scripta 37: 355-366. DOI: https://doi.org/10.1111/j.1463-6409.2008.00330.x
  19. Gamble, T., Colli, G.R., Rodrigues, M.T., Werneck, F.P., Simons, A.M. (2012): Phylogeny and cryptic diversity in geckos (Phyllopezus; Phyllodactylidae; Gekkota) from South America’s open biomes. Mol. Phylogenet. Evol. 62: 943-953. DOI: https://doi.org/10.1016/j.ympev.2011.11.033
  20. Gonçalves-Sousa, J.G., Cavalcante, L.A., Mesquita, D.O., Ávila, R.W. (2023): Determinants of resource use in lizard assemblages from the semiarid Caatinga, Brazil. Biotropica 55: 185-196. DOI: https://doi.org/10.1111/btp.13174
  21. Gonçalves-Sousa, J.G., Menezes, B.S., Fraga, R., Mesquita, D.O., Ávila, R.W. (2022): Riverine barrier and aridity effects on taxonomic, phylogenetic, and functional diversities of lizard assemblages from a semi-arid region. J. Biogeogr. 49: 1021-1033. DOI: https://doi.org/10.1111/jbi.14356
  22. Gonçalves-Sousa, J.G., Mesquita, D.O., Ávila, R.W. (2019): Structure of a Lizard Assemblage in a Semiarid Habitat of the Brazilian Caatinga. Herpetologica 75: 301-314. DOI: https://doi.org/10.1655/Herpetologica-D-19-00026.1
  23. Gotelli, N., Entsminger, G. (2004): EcoSim: Null models software for ecology. Version 7. Acquired Intelligence Inc. & Kesey-Bear. Jericho, VT 05465. Computer software. http://garyentsminger.com/ecosim/index.htm [accessed on 26 February 2024]
  24. Hammer, Ø., Harper, D.A., Ryan, P.D. (2001): PAST: Paleontological statistics software package for education and data analysis. Palaeontol. Electron. 4: 1-9.
  25. Huey, R.B. (1982): Temperature, physiology, and the ecology of reptiles. In: Biology of the Reptilia. Physiology, Vol. 12, pp. 25-91. Gans, C., and Pough, F.H., Eds, Academic Press, UK.
  26. Huey, R.B., Pianka, E.R. (1981): Ecological consequences of foraging mode. Ecology 62: 991-999. DOI: https://doi.org/10.2307/1936998
  27. Husak, J.F., Fox, S.F. (2008): Sexual selection on locomotor performance. Evol. Ecol. Res. 10: 213-228.
  28. Hutchinson, G. (1957): Concluding Remarks. Cold Spr. Harb. Symp. Quant. Biol, pp. 415-427. DOI: https://doi.org/10.1101/SQB.1957.022.01.039
  29. IPECE (2017): Missão Velha. Anuário Estatístico do Ceará. Perfil Básico dos Municípios. Available at https://www.ipece.ce.gov.br/wp-content/uploads/sites/45/2018/09/Missao_Velha_2017.pdf [accessed on 26 February 2024]
  30. Johnston, G., Bouskila, A. (2007): Sexual dimorphism and ecology of the gecko, Ptyodactylus guttatus. J. Herpetol. 41: 506-513. DOI: https://doi.org/10.1670/0022-1511(2007)41[506:SDAEOT]2.0.CO;2
  31. Kuo, C.-Y., MuñOz, M.M., Irschick, D.J. (2019): Lizard Foraging: A Perspective Integrating Sensory Ecology and Life Histories. In: Behavior of Lizards: Evolutionary and Mechanistic Perspectives, Vol. 1, pp. 87-105. Bels, V.L., and Russell, A.P., Eds, CRC Press, USA. DOI: https://doi.org/10.1201/9781498782739-4
  32. Lara-Resendiz, R.A., Arenas-Moreno, D., Valle-Jiménez, F.I. (2013a): Phyllodactylus tuberculosus (Yellow-Bellied Gecko). Body temperature. Herpetol. Rev. 44: 327-328.
  33. Lara-Resendiz, R.A., Arenas-Moreno, D.M., Méndez-De La Cruz, F.R. (2013b): Termorregulación diurna y nocturna de la lagartija Phyllodactylus bordai (Gekkota: Phyllodactylidae) en una región semiárida del centro de México. Rev. Chil. Hist. Nat. 86: 127-135. DOI: https://doi.org/10.4067/S0716-078X2013000200002
  34. Lima, D.C., Passos, D.C., Borges-Nojosa, D.M. (2011): Communal nests of Phyllopezus periosus, an endemic gecko of the Caatinga of northeastern Brazil. Salamandra 47: 227-228.
  35. Macarthur, R.H., Pianka, E.R. (1966): On optimal use of a patchy environment. Am. Nat. 100: 603-609. DOI: https://doi.org/10.1086/282454
  36. Massetti, F., Gomes, V., Perera, A., Rato, C., Kaliontzopoulou, A. (2017): Morphological and functional implications of sexual size dimorphism in the Moorish gecko, Tarentola mauritanica. Biol. J. Linn. Soc. 122: 197-209. DOI: https://doi.org/10.1093/biolinnean/blx060
  37. Mccluney, K.E., Sabo, J.L. (2009): Water availability directly determines per capita consumption at two trophic levels. Ecology 90: 1463-1469. DOI: https://doi.org/10.1890/08-1626.1
  38. Meiri, S., Avila, L., Bauer, A.M., Chapple, D.G., Das, I., Doan, T.M., Doughty, P., Ellis, R., Grismer, L., Kraus, F. (2020): The global diversity and distribution of lizard clutch sizes. Glob. Ecol. Biogeogr. 29: 1515-1530. DOI: https://doi.org/10.1111/geb.13124
  39. Mesquita, D.O., Costa, G.C., Colli, G.R., Costa, T.B., Shepard, D.B., Vitt, L.J., Pianka, E.R. (2016): Life-history patterns of lizards of the world. Am. Nat. 187: 689-705. DOI: https://doi.org/10.1086/686055
  40. Mochiutti, N.F., Guimarães, G.B., Moreira, J.C., Lima, F.F., Freitas, F.I. (2012): Os valores da geodiversidade: geossítios do Geopark Araripe/CE. Anu. Inst. Geoci. 35: 173-189. DOI: https://doi.org/10.11137/2012_1_173_189
  41. Neta, A.F.D.S., Ferreira, A.J.M.G., Oliveira, H.F.D., Silva, M.C.D., Avila, R.W. (2014): Geographical Distribution: Phyllopezus periosus. Herpetol. Rev. 45: 661.
  42. Nieva, R.A., Blanco, G.M., Acosta, J.C., Olmedo, M. (2013): Reproducción y dimorfismo sexual en una población de Homonota fasciata (Squamata: Phyllodactylidae) del monte de San Juan, Argentina. Rev. Mex. Biodiv. 84: 1266-1272. DOI: https://doi.org/10.7550/rmb.36045
  43. Olsson, M., Shine, R., Wapstra, E., Ujvari, B., Madsen, T. (2002): Sexual dimorphism in lizard body shape: the roles of sexual selection and fecundity selection. Evolution 56: 1538-1542. DOI: https://doi.org/10.1111/j.0014-3820.2002.tb01464.x
  44. Palmeira, C.N.S., Goncalves, U., Dantas Sales, R.F., Xavier Freire, E.M. (2021): Foraging behavior and diet composition of the gecko Phyllopezus periosus (Squamata: Phyllodactylidae) in the Brazilian semiarid Caatinga. Cuad. Herpetol. 35: 261-272.
  45. Passos, D.C., Zanchi, D., Duarte Rocha, C.F. (2013): Basking in shadows and climbing in the darkness: microhabitat use, daily activity and thermal ecology of the gecko Phyllopezus periosus Rodrigues, 1986. Herpetozoa 25: 171-174.
  46. Paulissen, M. (1999): Life history and drought tolerance of the parthenogenetic whiptail lizard Cnemidophorus laredoensis (Teiidae). Herpetol. Nat. Hist. 7: 41-57.
  47. Perry, G. (1995): The evolutionary ecology of lizard foraging: a comparative study. Unpublished Ph.D. Thesis. University of Texas, USA.
  48. Perry, G., Pianka, E.R. (1997): Animal foraging: past, present and future. Trends Ecol. Evol. 12: 360-364. DOI: https://doi.org/10.1016/S0169-5347(97)01097-5
  49. Pianka, E.R. (1973): The structure of lizard communities. Annu. Rev. Ecol. Syst. 4: 53-74. DOI: https://doi.org/10.1146/annurev.es.04.110173.000413
  50. Pianka, E.R., Vitt, L.J., Pelegrin, N., Fitzgerald, D.B., Winemiller, K.O. (2017): Toward a periodic table of niches, or exploring the lizard niche hypervolume. Am. Nat. 190: 601-616. DOI: https://doi.org/10.1086/693781
  51. Pinheiro, F., Diniz, I., Coelho, D., Bandeira, M. (2002): Seasonal pattern of insect abundance in the Brazilian cerrado. Aust. Ecol. 27: 132-136. DOI: https://doi.org/10.1046/j.1442-9993.2002.01165.x
  52. Powell, R., Parmelee, J.S., Rice, M.A., D, S.D. (1990): Ecological observations of Hemidactylus brooki haitianus Meerwath (Sauria: Gekkonidae) from Hispaniola. Caribb. J. Sci. 26: 67-70.
  53. Ragner, P., França, F., França, R., Silva, G. (2014): História natural do lagarto Phyllopezus periosus (Squamata: Phyllodactylidae) em um ambiente semi-árido no nordeste do Brasil. Revista Biociências 20: 5-12.
  54. R Core Team (2019): R: A language and environment for statistical computing. Version 3.6.1. R Foundation for Statistical Computing, Vienna, Austria.
  55. Recoder, R., Junior, M.T., Camacho, A., Rodrigues, M.T. (2012): Natural history of the tropical gecko Phyllopezus pollicaris (Squamata, Phyllodactylidae) from a sandstone outcrop in Central Brazil. Herpetol. Notes 5: 49-58.
  56. Ribeiro, S.C., Teles, D.A., Mesquita, D.O., Almeida, W.O., Anjos, L.a.D., Guarnieri, M.C. (2015): Ecology of the skink, Mabuya arajara Rebouças-Spieker, 1981, in the Araripe Plateau, northeastern Brazil. J. Herpetol. 49: 237-244. DOI: https://doi.org/10.1670/13-018
  57. Rodrigues, M. (1986): Uma nova espécie do gênero Phyllopezus de Cabaceiras: Paraíba: Brasil, com comentários sobre a fauna de lagartos da área (Sauria, Gekkonidae). Pap. Avulsos Zool. 36: 237-250. DOI: https://doi.org/10.5962/bhl.part.18420
  58. Saenz, D., Conner, R.N. (1996): Sexual dimorphism in head size of the Mediterranean gecko Hemidactylus turcicus (Sauria: Gekkonidae). Tex. J. Sci. 48: 207-212.
  59. Secor, S.M. (2009): Specific dynamic action: a review of the postprandial metabolic response. J. Comp. Physiol. B 179: 1-56. DOI: https://doi.org/10.1007/s00360-008-0283-7
  60. Simpson, E.H. (1949): Measurement of diversity. Nature 163: 688. DOI: https://doi.org/10.1038/163688a0
  61. Sinervo, B., Mendez-De-La-Cruz, F., Miles, D.B., Heulin, B., Bastiaans, E., Villagrán-Santa Cruz, M., Lara-Resendiz, R., Martínez-Méndez, N., Calderón-Espinosa, M.L., Meza-Lázaro, R.N. (2010): Erosion of lizard diversity by climate change and altered thermal niches. Science 328: 894-899. DOI: https://doi.org/10.1126/science.1184695
  62. Sousa, J.G.G., Ávila, R.W. (2015): Body size, reproduction and feeding ecology of Pleurodema diplolister (Amphibia: Anura: Leiuperidae) from Caatinga, Pernambuco state, Northeastern Brazil. Acta Herpetol. 10: 129-134.
  63. Sousa, J.G.G., Teixeira, A.a.M., Teles, D.A., Araújo-Filho, J.A., Ávila, R.W. (2017): Feeding ecology of two sympatric geckos in an urban area of Northeastern Brazil. Acta Herpetol. 12: 49-54.
  64. Uetz, P., Freed, P., Aguilar, R., Reyes, F., Hošek, J., (Eds.) (2022): The Reptile Database, http://www.reptile-database.org [accessed on 24 April 2023]
  65. Van Damme, R., Entin, P., Vanhooydonck, B., Herrel, A. (2008): Causes of sexual dimorphism in performance traits: a comparative approach. Evol. Ecol. Res. 10: 229-250.
  66. Vasconcellos, A., Andreazze, R., Almeida, A.M., Araujo, H.F., Oliveira, E.S., Oliveira, U. (2010): Seasonality of insects in the semi-arid Caatinga of northeastern Brazil. Rev. Bras. Entomol. 54: 471-476. DOI: https://doi.org/10.1590/S0085-56262010000300019
  67. Vitt, L.J. (1986): Reproductive tactics of sympatric gekkonid lizards with a comment on the evolutionary and ecological consequences of invariant clutch size. Copeia 3: 773-786. DOI: https://doi.org/10.2307/1444960
  68. Vitt, L.J. (1992): Diversity of reproductive strategies among Brazilian lizards and snakes: the significance of lineage and adaptation. In: Reproductive biology of South American vertebrates, Vol. 1, pp. 135-149. Hamlett, W.C., Ed, Springer, USA. DOI: https://doi.org/10.1007/978-1-4612-2866-0_10
  69. Vitt, L.J. (1995): The ecology of tropical lizards in the Caatinga of northeast Brazil. Oklahoma museum of Natural History 1: 1-29. DOI: https://doi.org/10.2307/1446894
  70. Vitt, L.J., Breitenbach, G.L. (1993): Life histories and reproductive tactics among lizards in the genus Cnemidophorus (Sauria: Teiidae). In: Biology of whiptail lizards (Genus Cnemidophorus), Vol 1, pp. 211-243. Wright, J., Vitt, L.J., Eds, Oklahoma Museum of Natural, USA.
  71. Vitt, L.J., Zani, P.A., Caldwell, J.P. (1996): Behavioural ecology of Tropidurus hispidus on isolated rock outcrops in Amazonia. J. Trop. Ecol. 12: 81-101. DOI: https://doi.org/10.1017/S0266467400009329
  72. Walter, G.H., Hengeveld, R. (2014): Autecology: organisms, interactions and environmental dynamics. CRC Press. DOI: https://doi.org/10.1201/b16805
  73. Wang, Y., Zeng, Z.-G., Li, S.-R., Bi, J.-H., Du, W.-G. (2016): Low precipitation aggravates the impact of extreme high temperatures on lizard reproduction. Oecologia 182: 961-971. DOI: https://doi.org/10.1007/s00442-016-3727-x
  74. Whiting, M.J., Mouton, P.L.F., Wyk, J.H.V., Cooper, W.E. (1999): Movement-and attack-based indices of foraging mode and ambush foraging in some gekkonid and agamine lizards from southern Africa. Amphibia-Reptilia 20: 391-399. DOI: https://doi.org/10.1163/156853899X00439

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