in

Predation risk is a function of seasonality rather than habitat complexity in a tropical semiarid forest

  • 1.

    Pianka, E. R. Niche relations of desert lizards in Ecology and Evolution of Communities, Cody, M. L. & Diamond, J. M. (Eds). (Harvard University Press, 1975).

  • 2.

    Castilla, A. M. & Labra, A. Predation and spatial distribution of the lizard Podarcis hipanica atrata: an experimental approach. Acta Oecol. 19, 107–114 (1998).

    ADS 
    Article 

    Google Scholar 

  • 3.

    Cantwell, L. R. & Forrest, T. G. Response of Anolis sagrei to acoustic calls from predatory and non-predatory birds. J. Herpetol. 47, 293–298 (2013).

    Article 

    Google Scholar 

  • 4.

    Edmund, M. Defense in animals: A survey of antipredator defenses. (Longman Press, 1974).

  • 5.

    Wilcove, D. Nest predation in forest tracts and the decline of migratory songbirds. Ecology 66, 121l-l214 (1985).

    Article 

    Google Scholar 

  • 6.

    Endler, J. A. Defense against predators in Predator-prey relationships, Feder, M. E. & Lauder, G. V. (Eds). (The University of Chicago Press, 1986).

  • 7.

    Constantini, D., Bruner, E., Fanfani, A. & Dell’Omo, G. Male-biased predation of western green lizards by Eurasian kestrels. Naturwissenschaften 94, 1015–1020. https://doi.org/10.1007/s00114-007-0284-5 (2007).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 8.

    Barnett, A. A. et al. Run, hide or fight: anti-predation strategies in Endangered red-nosed cuxiú (Chiropotes albinasus, Pitheciidae) in south-eastern Amazonia. Primates 58, 353–360. https://doi.org/10.1007/s10329-017-0596-9 (2017).

    Article 
    PubMed 

    Google Scholar 

  • 9.

    Barnett, A. A. et al. Honest error, precaution or alertness advertisement? Reactions to vertebrate pseudopredators in red-nosed cuxiús (Chiropotes albinasus), a high-canopy neo-tropical primate. Ethology 124, 177–187. https://doi.org/10.1111/eth.12721 (2018).

    Article 

    Google Scholar 

  • 10.

    Roslin, T. et al. Higher predation risk for insect prey at low latitudes and elevations. Science 356, 742–744. https://doi.org/10.1126/science.aaj1631 (2017).

    ADS 
    CAS 
    Article 
    PubMed 

    Google Scholar 

  • 11.

    Shepard, D. B. Habitat but not body shape affects predator attack frequency on lizard models in the Brazilian Cerrado. Herpetologica 63, 193–202. https://doi.org/10.1655/0018-0831(2007)63[193:HBNBSA]2.0.CO;2 (2007).

    Article 

    Google Scholar 

  • 12.

    Salvidio, S., Costa, A. & Romano, A. The use of clay models in amphibian field studies: a short review. Bull. Env. Life Sc. 1, 8 (2019).

    Google Scholar 

  • 13.

    Castilla, A. M., Gosá, A., Galán, P. & Pérez-Mellado, V. Green tails in lizards of the genus Podarcis: do they influence the intensity of predation?. Herpetologica 55, 530–537 (1999).

    Google Scholar 

  • 14.

    Bateman, P. W., Fleming, P. A. & Wolfe, A. K. A different kind of ecological modelling: the use of clay model organisms to explore predator-prey interactions in vertebrates. J. Zool. 301, 251–262. https://doi.org/10.1111/jzo.12415 (2017).

    Article 

    Google Scholar 

  • 15.

    Rössler, D., Pröhl, H. & Lötters, S. The future of clay model studies. BMC Zool. 3, 6. https://doi.org/10.1186/s40850-018-0033-6 (2018).

    Article 

    Google Scholar 

  • 16.

    Major, R. E. & Kendal, C. E. The contribution of artificial nest experiments to understanding avian reproductive success: a review of methods and conclusions. Ibis 138, 298–307 (1996).

    Article 

    Google Scholar 

  • 17.

    Kuchta, S. R. Experimental support for aposematic coloration in the salamander Ensatina eschscholtzii xanthoptica: implications for mimicry of Pacific newts. Copeia 267–271, 2005. https://doi.org/10.1643/CH-04-173R (2005).

    Article 

    Google Scholar 

  • 18.

    Kraemer, A. C., Serb, J. M. & Adams, D. C. Both novelty and conspicuousness influence selection by mammalian predators on the colour pattern of Plethodon cinereus (Urodela: Plethodontidae). Biol. J. Linn. Soc. 118, 889–900. https://doi.org/10.1111/bij.12780 (2016).

    Article 

    Google Scholar 

  • 19.

    Salvidio, S., Palumbi, G., Romano, A. & Costa, A. Safe caves and dangerous forests? Predation risk may contribute to salamander colonization of subterranean habitats. Sci. Nat. 104, 3–4. https://doi.org/10.1007/s00114-017-1443-y (2017).

    CAS 
    Article 

    Google Scholar 

  • 20.

    Mcelroy, M. T. Teasing apart crypsis and aposematism-evidence that disruptive coloration reduces predation on a noxious toad. Biol. J. Linn. Soc. 17, 285–294. https://doi.org/10.1111/bij.12669 (2016).

    Article 

    Google Scholar 

  • 21.

    Nordberg, E. J. & Schwarzkopf, L. Predation risk is a function of alternative prey availability rather than predator abundance in a tropical savanna woodland ecosystem. Sci. Rep. 9, 7718. https://doi.org/10.1038/s41598-019-44159-6 (2019).

    ADS 
    CAS 
    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • 22.

    Costa, A., Coroller, S. & Salvidio, S. Comparing day and night predation rates on lizard-Like clay models. Herpetol. Conserv. Biol. 15, 198–203 (2020).

    Google Scholar 

  • 23.

    Nour, N., Matthysen, E. & Dhondt, A. A. Artificial nest predation and habitat fragmentation: different trends in birds and mammal predators. Ecography 16, 111–116 (1993).

    Article 

    Google Scholar 

  • 24.

    Castilla, A. M. Intensive predation of Audouin’s Gull nests by the yellow legged gull in the Columbretes islands. Colon Waterbirds 18, 226–230. https://doi.org/10.2307/1521487 (1995).

    Article 

    Google Scholar 

  • 25.

    Diego-Rasilla, F. J. Influence of predation pressure on the escape behaviour of Podarcis muralis lizards. Behav. Processes 63, 1–7. https://doi.org/10.1016/S0376-6357(03)00026-3 (2003).

    Article 
    PubMed 

    Google Scholar 

  • 26.

    Stuart-fox, D. M., Moussalli, A., Marshall, N. J. & Owens, I. P. F. Conspicuous males suffer higher predation risk: Visual modeling and experimental evidence from lizards. Anim. Behav. 66, 541–550. https://doi.org/10.1006/anbe.2003.2235 (2003).

    Article 

    Google Scholar 

  • 27.

    Husak, J. F., Macedonia, J. M., Fox, S. F. & Sauceda, R. C. Predation cost of conspicuous male coloration in collared lizards (Crotaphytus collaris): an experimental test using clay-covered model lizards. Ethology 112, 572–580. https://doi.org/10.1111/j.1439-0310.2005.01189.x (2006).

    Article 

    Google Scholar 

  • 28.

    Keehn, J. E. & Feldman, C. R. Predator attack rates and anti-predator behavior of Side-blotched Lizards (Uta stransbuiana) at Southern California Wind Farms, USA. Herpetol. Conserv. Biol. 13, 194–204 (2018).

    Google Scholar 

  • 29.

    Hansen, N. A., Sato, C. F., Michael, D. L., Lindenmayer, D. B. & Driscoll, D. A. Predation risk for reptiles is highest at remnant edges in agricultural landscapes. J. Appl. Ecol. 56, 31–43. https://doi.org/10.1111/1365-2664.13269 (2019).

    Article 

    Google Scholar 

  • 30.

    Hegna, R. H., Saporito, R. A., Gerow, K. G. & Donnelly, M. A. Contrasting colours in an aposematic frog do not affect predation. Ann. Zool. 48, 29–38. https://doi.org/10.5735/086.048.0103 (2011).

    Article 

    Google Scholar 

  • 31.

    Paluh, D. J., Hantak, M. M. & Saporito, R. A. A test of aposematism in the dendrobatid poison frog Oophaga pumilio: the importance of movement in clay model experiments. J. Herpetol. 48, 249–254. https://doi.org/10.1670/13-027 (2014).

    Article 

    Google Scholar 

  • 32.

    Rojas, D. P., Stow, A., Amézquita, A., Simões, P. I. & Lima, A. P. No predatory bias with respect to colour familiarity for the aposematic Adelphobates galactonotus (Anura: Dendrobatidae). Behaviour 152, 1637–165. https://doi.org/10.1163/1568539X-00003297 (2015).

    Article 

    Google Scholar 

  • 33.

    Brodie, E. D. I. I. I. Differential avoidance of coral snake banded patterns by free-ranging avian predators in Costa Rica. Evolution 47, 227–235. https://doi.org/10.1111/j.1558-5646.1993.tb01212.x (1993).

    Article 
    PubMed 

    Google Scholar 

  • 34.

    Brodie, E. D. I. I. I. & Janzen, F. J. Experimental studies of coral snake mimicry: Generalized avoidance of ringed snake patterns by free-ranging avian predators. Funct. Ecol. 9, 186–190. https://doi.org/10.2307/2390563 (1995).

    Article 

    Google Scholar 

  • 35.

    Pfennig, D. W., Harper, G. R. Jr., Brumo, A. F., Harcombe, W. R. & Pfennig, K. S. Population differences in predation on Batesian mimics in allopatry with their model: Selection against mimics is strongest when they are common. Behav. Ecol. Sociobiol. 61, 505–511. https://doi.org/10.1007/s00265-006-0278-x (2006).

    Article 

    Google Scholar 

  • 36.

    Martín, J. & López, P. An experimental test of the costs of antipredatory refuge use in the wall lizard, Podarcis muralis. Oikos 84, 499–505 (1999).

    Article 

    Google Scholar 

  • 37.

    Amo, L., López, P. & Martín, J. Refuge use: a conflict between avoiding predation and losing mass in lizards. Physiol. Behav. 90, 334–343. https://doi.org/10.1016/j.physbeh.2006.09.035 (2007).

    CAS 
    Article 
    PubMed 

    Google Scholar 

  • 38.

    Endler, J. A. Interactions between predators and prey in Behavioural Ecology: An Evolutionary Approach, Krebs, J. R. & Davies, N. B., (Eds). (Blackwell, 1991).

  • 39.

    Denno, R. F., Finke, D. L. & Langellotto, G. A. Direct and indirect effects of vegetation structure and habitat complexity on predator-prey and predator-predator interactions in Ecology of Predator-prey Interactions, Barbosa, P. & Castellanos, I. (Eds). (Oxford University Press, 2005).

  • 40.

    Ruxton, G. D., Sherratt, T. N. & Speed, M. P. Avoiding Attack: The evolutionary ecology of crypsis, warning signals, and mimicry. (Oxford University Press, 2004).

  • 41.

    Sih, A. To hide or not to hide? Refuge use in a fluctuating environment. Trends Ecol. Evol. 12, 375–6 (1997).

    CAS 
    Article 

    Google Scholar 

  • 42.

    Martín, J., López, P. & Cooper, W. E. Jr. When to come out from a refuge: balancing predation risk and foraging opportunities in an alpine lizard. Ethology 109, 77–87. https://doi.org/10.1046/j.1439-0310.2003.00855.x (2003).

    Article 

    Google Scholar 

  • 43.

    Bulova, S. J. Ecological correlates of population and individual variation in antipredator behaviour of two species of desert lizards. Copeia 4, 980–992. https://doi.org/10.2307/1446721 (1994).

    Article 

    Google Scholar 

  • 44.

    Vanhooydonck, B. & Van Damme, R. Relationships between locomotor performance, microhabitat use and antipredator behaviour in lacertid lizards. Func. Ecol. 17, 160–169. https://doi.org/10.1046/j.1365-2435.2003.00716.x (2003).

    Article 

    Google Scholar 

  • 45.

    Vervust, B., Grbac, I. L. & Van Damme, R. Differences in morphology, performance and behavior between recently diverged populations of Podarcis sicula mirror differences in predation pressure. Oikos 116, 1343–1352. https://doi.org/10.1111/j.2007.0030-1299.15989.x (2007).

    Article 

    Google Scholar 

  • 46.

    Smith, G. R. & Ballinger, R. E. The ecological consequences of habitat and microhabitat use in lizards: a review. Contemp. Herpetol. 3, 1–13. https://doi.org/10.1002/3527600213.ch1 (2001).

    Article 

    Google Scholar 

  • 47.

    Wüster, W. et al. Do aposematism and Batesian mimicry require bright colours? A test, using European viper markings. Proc. Roy. Soc. London 271, 2495–2499. https://doi.org/10.1098/rspb.2004.2894 (2004).

    Article 

    Google Scholar 

  • 48.

    Worthington-Hill, O. & Gill, A. Effects of large-scale heathland management on thermal regimes and predation on adders Vipera berus. Anim. Conserv. 22, 481–492. https://doi.org/10.1111/acv.12489 (2019).

    Article 

    Google Scholar 

  • 49.

    Chiang, J. C. H. & Koutavas, A. Tropical flip-flop connection. Nature 432, 684–685. https://doi.org/10.1038/432684a (2004).

    ADS 
    CAS 
    Article 
    PubMed 

    Google Scholar 

  • 50.

    Carmo, R. F. R., Amorim, H. P. & Vasconcelos, S. D. Scorpion diversity in two types of seasonally dry tropical forest in the semi-arid region of Northeastern Brazil. Biota. Neotrop. 13, 340–344. https://doi.org/10.1590/S1676-06032013000200037 (2013).

    Article 

    Google Scholar 

  • 51.

    Warrick, G. D., Kato, T. T. & Rose, B. R. Microhabitat use and home range characteristics of Blunt-nosed leopard lizards. J. Herpetol. 32, 183–191 (1998).

    Article 

    Google Scholar 

  • 52.

    Constantini, D. & Dell’Omo, G. Sex-Specific predation on two lizard species by kestrels. Russ. J. Ecol. 41, 99–101. https://doi.org/10.1134/S1067413610010182 (2010).

    Article 

    Google Scholar 

  • 53.

    Poulin, B. et al. Avian predation upon lizards and frogs in a neotropical forest understory. J. Trop. Ecol. 17, 21–40. https://doi.org/10.1017/S026646740100102X (2001).

    Article 

    Google Scholar 

  • 54.

    Araújo, C. S., Candido, D. M., Araújo, H. F. P., Dias, S. C. & Vasconcellos, A. Seasonal variations in scorpion activities (Arachnida: Scorpiones) in an area of Caatinga vegetation in Northeastern Brazil. Zoologia 27, 372–376. https://doi.org/10.1590/S1984-46702010000300008 (2010).

    Article 

    Google Scholar 

  • 55.

    Vasconcellos, A. et al. Seasonality of insects in the semi-arid Caatinga of northeastern Brazil. Rev. Bras. Entomol. 54, 471–476. https://doi.org/10.1590/S0085-56262010000300019 (2010).

    Article 

    Google Scholar 

  • 56.

    Schall, J. J. & Pianka, E. R. Evolution of escape behavior diversity. Am. Nat. 115, 551–566 (1980).

    Article 

    Google Scholar 

  • 57.

    Martín, J. & López, P. Influence of habitat structure on the escape tactics of the lizard Psammodromus algirus. Can. J. Zool. 73, 129–132 (1995).

    Article 

    Google Scholar 

  • 58.

    Rocha, C. F. D. & Bergallo, H. G. Intercommunity variation in the distribution of abundance of dominant lizard species in restinga habitats. Ciencia e Cultura 49, 269–274 (1997).

    Google Scholar 

  • 59.

    Van-Sluys, M. Growth and body condition of the saxicolous lizard Tropidurus itambere in southeastern Brazil. J. Herpetol. 32, 359–365 (1998).

    Article 

    Google Scholar 

  • 60.

    Liebezeit, J. R. & Zack, S. Point counts underestimate the importance of arctic foxes as avian nest predators: evidence from remote video cameras in arctic Alaskan oil fields. Arctic 61, 153–161 (2008).

    Google Scholar 

  • 61.

    DeGregorio, B. A., Weatherhead, P. J. & Sperry, J. H. Power lines, roads, and avian nest survival: effects on predator identity and predation intensity. Ecol. Evol. 4, 1589–1600. https://doi.org/10.1002/ece3.1049 (2014).

    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • 62.

    Huey, R. B. & Pianka, E. R. Ecological consequences of foraging mode. Ecology 62, 991–999 (1981).

    Article 

    Google Scholar 

  • 63.

    Greene, H. W. Antipredator mechanisms in reptiles in Biology of Reptilian, Gans, C. & Huey, R. B. (Eds.). (Springer, 1998).

  • 64.

    Martín, J. & López, P. Amphibians and reptiles as prey of birds in southwestern Europe. Smit. Herpetol. Inform. Serv. 82, 1–43 (1990).

    Google Scholar 

  • 65.

    Steffen, J. E. Perch-height specific predation on tropical lizard clay models: implications for habitat selection in mainland neotropical lizards. Rev. Biol. Trop. 57, 859–864. https://doi.org/10.15517/rbt.v57i3.5498 (2009).

    Article 
    PubMed 

    Google Scholar 

  • 66.

    Dunham, A. E., Grant, B. W. & Overall, K. L. Interfaces between biophysical and physiological ecology and the population ecology of terrestrial vertebrate ectotherms. Physiol. Zool. 62, 335–355 (1989).

    Article 

    Google Scholar 

  • 67.

    Ruiz-Esparza, J. et al. Birds of the Grota do Angico Natural Monument in the semi-arid Caatinga scrublands of northeastern Brazil. Biota. Neotrop. 11, 1–8. https://doi.org/10.1590/S1676-06032011000200027 (2011).

    Article 

    Google Scholar 

  • 68.

    Lima, C. P., Santos, S. S. & Lima, R. C. Levantamento e Anilhamento da Ornitofauna na Pátria da Arara-Azul-de-Lear (Anodorhynchus leari, Bonaparte, 1856): um complemento ao Levantamento realizado por Sick, H., Gonzaga, L. P. e Teixeira, D. M., 1987. Atual. Ornitol. 112, 11–22 (2003).

  • 69.

    Roos, A. L. et al. Avifauna da região do Lago de Sobradinho: composição, riqueza e biologia. Ornithologia 1, 135–160 (2006).

    Google Scholar 

  • 70.

    Farias, G. B., Pereira, G. P. & Burgos, K. Q. Aves da Floresta Nacional de Negreiros (Serrita, Pernambuco). Atual. Ornitol. 157, 41–46 (2010).

    Google Scholar 

  • 71.

    Sousa, P. A. G. & Freire, E. M. X. Coleodactylus natalensis (NCN). Predation. Herpetol. Rev. 41, 218 (2010).

    Google Scholar 

  • 72.

    Ribeiro, L. B., Gogliath, M. & Freire, E. M. X. Hemidactylus brasilianus (Amaral’s Brazilian Gecko) and Cnemidophorus ocellifer (Spix`s Whiptail). Predation. Herpetol. Bull. 117, 31–32 (2011).

    Google Scholar 

  • 73.

    De-Carvalho, C. B. et al. Gymnodactylus geckoides (Naked-Toed Gecko): Predation. Herpetol. Bull. 121, 41–43 (2012).

    Google Scholar 

  • 74.

    McCormick, S. & Polis, G. A. Arthropods that prey on vertebrates. Biol. Rev. 57, 29–58 (1982).

    Article 

    Google Scholar 

  • 75.

    Rocha, C. F. D. & Vrcibradic, D. Reptiles as predators of vertebrates and as preys in a restinga habitat of southeastern Brazil. Ciencia e Cultura 50, 364–368 (1998).

    Google Scholar 

  • 76.

    Armas, L. F. Frogs and lizards as prey of some Greater Antillean arachnids. Rev. Iberica Aracnol. 3, 87–88 (2000).

    Google Scholar 

  • 77.

    Schatz, B., Suzzoni, J. P., Corbara, B. & Dejean, A. Selection and capture of prey in the African ponerine ant Plectroctena minor (Hymenoptera: formicidae). Acta Oecol. 22, 55–60. https://doi.org/10.1016/S1146-609X(00)01100-0 (2001).

    ADS 
    Article 

    Google Scholar 

  • 78.

    Nordberg, E. J., Edwards, L. & Schwarzkopf, L. Terrestrial invertebrates: an underestimated predator guild for small vertebrate groups. Food Webs 15, e00080 (2018).

    Article 

    Google Scholar 

  • 79.

    Seifert, C. L., Schulze, C. H., Dreschke, T. C. T., Frötscher, H. & Fiedler, K. Day vs. night predation on artificial caterpillars in primary rainforest habitats-an experimental approach. Entomol. Exp. Appl. 158, 54–59. https://doi.org/10.1111/eea.12379 (2016).

    Article 

    Google Scholar 

  • 80.

    Andrade, L. A., Pereira, I. M., Leite, U. T. & Barbosa, M. R. V. Análise da cobertura de duas fitofisionomias de Caatinga, com diferentes históricos de uso, no município de São João do Cariri, estado da Paraíba. Cerne 11, 253–262 (2005).

    Google Scholar 

  • 81.

    Castelletti, C. H. M., Silva, J. M. C., Tabarelli, M. & Santos, A. M. M. Quanto ainda resta da Caatinga? Uma estimative preliminar in Biodiversidade da Caatinga: áreas e ações prioritárias para a conservação, Silva, J. M. C., Tabarelli, M., Fonseca, M. T. & Lins, L. V. (Eds.). (Ministério do Meio Ambiente Publishing, 2004).

  • 82.

    Albuquerque, U. P. et al. Caatinga revisited: ecology and conservation of an important seasonal dry forest. Sci. World J. 1–18, 2012. https://doi.org/10.1100/2012/205182 (2012).

    Article 

    Google Scholar 

  • 83.

    Da Silva, A. C. C., Prata, A. P. N. & Mello, A. A. Flowering plants of the Grota do Angico Natural Monument, Caatinga of Sergipe, Brazil. Check List 9, 733–739 (2013).

    Article 

    Google Scholar 

  • 84.

    Nimer, E. Climatologia da Região Nordeste do Brasil: Introdução à Climatologia Dinâmica. Rev. Bras. Geog. 34, 3–51 (1972).

    Google Scholar 

  • 85.

    Santos, A. F. & Andrade, J. A. O quadro natural: caracterização e delimitação do semi-árido sergipano. Sergipe. Brazil. (CNPq/UFS, 1992).

  • 86.

    SEMARH–Secretaria de Estado do Meio Ambiente e dos Recursos Hídricos. Plano de Manejo do Monumento Natural Grota do Angico. Sergipe, Brazil. (Secretaria de Estado do Meio Ambiente e dos Recursos Hídricos, 2011)

  • 87.

    Ferreira, A. S., Silva, A. O., Conceição, B. M. & Faria, R. G. The diet of six species of lizards in an area of Caatiga, Brazil. Herpetol. J. 27, 151–160 (2017).

    Google Scholar 

  • 88.

    Rocha, S. M. et al. Lizards from the Alto Sertão region of Sergipe state, northeastern Brazil. Biota Neotrop. 21(2), e20201137 (2021).

    Article 

    Google Scholar 

  • 89.

    Bennett, A. T. D., Cuthill, I. C. & Norris, K. J. Sexual selection and the mismeasure of color. Am. Nat. 144, 848–860 (1994).

    Article 

    Google Scholar 

  • 90.

    Niskanen, M. & Mappes, J. Significance of the dorsal zigzag pattern of Vipera latastei gaditana against avian predators. J. Anim. Ecol. 74, 1091–1101. https://doi.org/10.1111/j.1365-2656.2005.01008.x (2005).

    Article 

    Google Scholar 

  • 91.

    R Core Team. R: A language and environment for statistical computing (2020).


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