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  • Cited by 13
  • Print publication year: 2007
  • Online publication date: August 2010

1 - Movement patterns in lizards: measurement, modality, and behavioral correlates

Summary

From the least to the greatest in the zoological progression, the stomach sways the world.

(Fabre, 1913)

Introduction

To reproduce successfully, an organism must survive, attain suitable size, attract a mate, and produce viable offspring. All of these activities require that the individual obtain considerable amounts of energy. Foraging success can thus strongly impact reproductive success (Travers and Sih, 1991; Bernardo, 1994; Nilsson, 1994). Reproductive success is the fabric upon which natural selection works (Darwin, 1859). Evolutionary biologists and behavioral ecologists, starting with the pioneering work of MacArthur and Pianka (1966) and Emlen (1966), have therefore shown considerable interest in foraging behaviors and their correlates. The resulting literature is voluminous and often contentious: too much so for a single chapter, or even volume, to effectively summarize. In keeping with the theme of this book, I focus on the issue of bimodality in lizard foraging behavior, its phylogenetic background, and its putative correlates.

Before one can discuss patterns, however, methodological issues must be clarified. This chapter is therefore divided into two main sections. The first section focuses on some previously neglected methodological issues related to measurement of foraging behavior. Establishing these is crucial for ensuring data quality in the analyses that follow. The second section then concentrates on testing theoretical predictions of foraging theory, and on some conceptual consequences of what has been learned to date. Because the literature is so extensive, I frequently limit the use of references to representative examples throughout this chapter.

References
Anderson, R. A. (1993). An analysis of foraging in the lizard, Cnemidophorus tigris. In Biology of Whiptail Lizards (Genus Cnemidophorus), ed. Wright, J. W. and Vitt, L. J., pp. 83–116. Norman, OK: Oklahoma Museum of Natural History.
Andrews, R. M. (1979a). The lizard Corytophanes cristatus: an extreme “sit-and-wait” predator. Biotropica 11, 136–9.
Andrews, R. M. (1979b). Evolution of life histories: a comparison of Anolis lizards from matched island and mainland habitats. Breviora 454, 1–51.
Avery, R. A., Mueller, C. F., Jones, S. M., Smith, J. A. and Bond, D. L. (1987). The movement patterns of lacertid lizards: a comparative study. J. Herpetol. 21, 324–9.
Avital, E. (1981). Resource partitioning between two lizard species of the genus Acanthodactylus living in the same area of sands. M.Sc. thesis, Hebrew University of Jerusalem. (In Hebrew.)
Bell, W. J. (1991). Searching Behaviour. London: Chapman and Hall.
Bernardo, J. (1993). Determinants of maturation in animals. Trends Ecol. Evol. 8, 166–73.
Bernardo, J. (1994). Experimental analysis of allocation in two divergent, natural salamander populations. Am. Nat. 143, 14–38.
Biro, P. A. and Ridgway, M. S. (1995). Individual variation in foraging movement in a lake population of young-of-the-year brook charr (Salvelinus fontinalis). Behaviour 132, 57–74.
Bonine, K. E. and Garland, T. Jr. (1999). Sprint performance of phrynosomatid lizards, measured on a high-speed treadmill, correlates with hindlimb length. J. Zool. Lond. 248, 255–65.
Borror, D. J., Triplehorn, C. A. and Johnson, N. F. (1989). An Introduction to the Study of Insects. Philadelphia, PA: Saunders.
Castanzo, R. A. and Bauer, A. M. (1993). Diet and activity of Mabuya acutilabris (Reptilia: Scincidae) in Namibia. Herpetol. J. 3, 130–5.
Cooper, W. E Jr. (1994). Prey chemical discrimination, foraging mode, and phylogeny. In Lizard Ecology: Historical and Experimental Perspectives, ed. Vitt, L. J. and Pianka, E. R., pp. 95–116. Princeton, NJ: Princeton University Press.
Cooper, W. E. Jr. (1995). Foraging mode, prey chemical discrimination, and phylogeny in lizards. Anim. Behav. 50, 973–85.
Cooper, W. E. Jr. and Whiting, M. J. (1999). Foraging modes in lacertid lizards from southern Africa. Amph.-Rept. 20, 299–311.
Cooper, W. E. Jr. and Whiting, M. J. (2000). Ambush and active foraging modes both occur in the scincid genus Mabuya. Copeia 2000, 112–18.
Cooper, W. E. Jr., Vitt, L. J., Caldwell, J. P. and Fox, S. F. (2001). Foraging modes of some American lizards: relationships among measurement variables and discreteness of modes. Herpetologica 57, 65–76.
Cooper, W. E. Jr., Whiting, M. J. and Wyk, J. H. (1997). Foraging modes of cordyliform lizards. S. Afr. J. Zool. 32, 9–13.
Cooper, W. E. Jr., Whiting, M. J., Wyk, J. H. and Mouton, P. F. N. (1999). Movement- and attack-based indices of foraging mode and ambush foraging in some gekkonid and agamine lizards from southern Africa. Amph.-Rept. 20, 391–9.
Darwin, C. (1859). On the Origin of Species. London: John Murray.
Dmi'el, R., Perry, G. and Lazell, J. (1997). Evaporative water loss in nine insular populations of the Anolis cristatellus group in the British Virgin Islands. Biotropica 29, 111–16.
Dubas, G. (1987). Biotic determinants of home range size of the scincid lizard Trachydosaurus rugosus (Gray). Ph.D. thesis, Flinders University.
Dubas, G. and Bull, C. M. (1991). Diet choice and food availability in the omnivorous lizard, Trachydosaurus rugosus. Wild. Res. 18, 147–55.
Durtsche, R. D. (1992). Feeding time strategies of the fringe-toed lizard, Uma inornata, during breeding and non-breeding seasons. Oecologia 89, 85–9.
du Toit, A., Mouton, P. L. N., Geertsema, H. and Flemming, A. F. (2002). Foraging mode of serpentiform, grass-living cordylid lizards: a case study of Cordylus anguina. Afr. Zool. 37, 141–9.
Eifler, D. A. and Eifler, M. A. (1998). Foraging behavior and spacing patterns of the lizard Cnemidophorus uniparens. J. Herpetol. 32, 24–33.
Eifler, D. A. and Eifler, M. A. (1999). Foraging behavior and spacing patterns of the lizard Oligosoma grande. J. Herpetol. 33, 632–9.
Ellinger, N., Schlatte, G., Jerome, N. and Hödl, W. (2001). Habitat use and activity patterns of the neotropical arboreal lizard Tropidurus (= Uracentron) azureus werneri (Tropiduridae). J. Herpetol. 35, 395–402.
Emlen, J. M. (1966). The role of time and energy in food preference. Am. Nat. 100, 611–17.
Fabre, J. H. (1913). The Life of the Fly. London: Hodder and Stoughton.
Felsenstein, J. (1985). Phylogenies and the comparative method. Am. Nat. 125, 1–15.
Fitch, H. S. (1970). Reproductive cycles in lizards and snakes. Univ. Kansas Mus. Nat. Hist. Misc. Pub. 52, 1–247.
Fitzpatrick, J. W. (1981). Search strategies of tyrant flycatchers. Anim. Behav. 29, 810–21.
Fuiman, L. A. and Cowan, J. H. (2003). Behavior and recruitment success in fish larvae: repeatability and covariation of survival skills. Ecology 84, 53–67.
Garland, T. Jr., Dickerman, A. W., Janis, C. M. and Jones, J. A. (1993). Phylogenetic analysis of covariance by computer simulation. Syst. Biol. 42, 265–92.
Garland, T. Jr., Harvey, P. H. and Ives, A. R. (1992). Procedures for the analysis of comparative data using phylogenetically independent contrasts. Syst. Biol. 41, 18–32.
Gasnier, T. R., Magnusson, W. E. and Lima, A. P. (1994). Foraging activity and diet of four sympatric lizard species in a tropical rainforest. J. Herpetol. 28, 187–92.
Gerritsen, J. and Strickler, J. R. (1977). Encounter probabilities and community structure in zooplankton: a mathematical model. J. Fish. Res. Board Can. 34, 73–82.
Grafen, A. (1989). The phylogenetic regression. Phil. Trans. R. Soc. Lond. B326, 19–157.
Greeff, J. M. and Whiting, M. J. (2000). Foraging-mode plasticity in the Augrabies flat lizard Platysaurus broadleyi. Herpetologica 56, 402–7.
Hirth, H. F. (1963). The ecology of two lizards on a tropical beach. Ecol. Monogr. 33, 83–112.
Honda, M., Ota, H., Köhler, G.et al. (2003). Phylogeny of the lizard subfamily Lygosominae (Reptilia: Scincidae), with special reference to the origin of the New World taxa. Gen. Genet. Syst. 78, 71–80.
Huey, R. B. and Pianka, E. R. (1981). Ecological consequences of foraging mode. Ecology 62, 991–9.
Huey, R. B., Pianka, E. R. and Vitt, L. J. (2001). How often do lizards run on empty? Ecology 82, 1–7.
Husak, J. F. and Ackland, E. N. (2003). Foraging mode of the reticulate collared lizard, Crotaphytus reticulatus. Southw. Nat. 48, 282–6.
Irschick, D. J. (2000). Comparative and behavioral analyses of preferred speed: Anolis lizards as a model system. Physiol. Biochem. Zool. 73, 428–37.
Kareiva, P. (1989). Renewing the dialogue between theory and experiments in population ecology. In Perspectives in Ecological Theory, ed. Roughgarden, J., May, R. M. and Levin, S. A., pp. 68–88. Princeton, N.J.: Princeton University Press.
Krebs, J. R. and Kacelnik, A. (1991). Decision-making. In Behavioural Ecology, 3rd edn, ed. Krebs, J. R. and Davies, N. B., pp. 105–36. London: Blackwell Scientific.
Lawton, J. (1991). Ecology as she is done, and could be done. Oikos 61, 289–90.
Levins, R. (1966). The strategy of model building in population biology. Am. Sci. 54, 421–31.
Lewis, A. R. (1989). Diet selection and depression of prey abundance by an intensively foraging lizard. J. Herpetol. 23, 164–70.
Lewis, A. R. and Saliva, J. (1987). Effects of sex and size on home range, dominance, and activity budgets in the Puerto Rican teiid Ameiva exsul (Lacertilia: Teiidae). Herpetologica 43, 374–83.
Lister, B. C. (1981). Seasonal niche relationships of rain forest anoles. Ecology 62, 1548–60.
Losos, J. B., Jackman, T. R., Larson, A., Queiroz, K. and Rodríguez-Schettino, L. (1998). Contingency and determinism in replicated adaptive radiations of island lizards. Science 279, 2115–18.
MacArthur, R. H. and Pianka, E. R. (1966). On optimal use of a patchy environment. Am. Nat. 100, 603–9.
Mac Nally, R. C. (1994). On characterizing foraging versatility, illustrated by using birds. Oikos 69, 95–106.
Magnusson, W. E. and da Silva, E. V. (1993). Relative effects of size, season and species on the diets of some Amazonian savanna lizards. J. Herpetol. 27, 380–5.
Magnusson, W. E., Paiva, L. J., da Rocha, R. M.et al. (1985). The correlates of foraging mode in a community of Brazilian lizards. Herpetologica 41, 324–32.
Mausfeld, P., Vences, M., Schmitz, A. and Veith, M. (2000). First data on molecular phylogeography of scincid lizards of the genus Mabuya. Molec. Phylog. Evol. 17, 11–14.
McLaughlin, R. L. (1989). Search modes of birds and lizards: evidence for alternative movement patterns. Am. Nat. 133, 654–70.
Mori, A. and Randriamahazo, H. J. A. R. (2002). Foraging mode of a Madagascan iguanian lizard, Oplurus cuvieri cuvieri. Afr. J. Ecol. 40, 61–4.
Mouton, P. F. N., Geertsema, H. and Visagie, L. (2000). Foraging mode of a group-living lizard, Cordylus cataphractus (Cordylidae). Afr. Zool. 35, 1–7.
Muth, A. (1992). Development of baseline data and procedures for monitoring populations of the flat-tailed horned lizard, Phrynosoma mcallii. Final report for California Dept. of Fish and Game contract 86/87 C-2056 and 87/88 C-2056.
Nilsson, J.-A. (1994). Energetic bottle-necks during breeding and the reproductive cost of being too early. J. Anim. Ecol. 63, 200–8.
Orr, Y., Shachak, M. and Steinberger, Y. (1979). Ecology of the small spotted lizard (Eremias guttulata guttulata) in the Negev desert (Israel). J. Arid Env. 2, 151–61.
Orzack, S. H. and Sober, E. (1994). How (not) to test an optimality model. Trends Ecol. Evol. 9, 265–7.
Paulissen, M. A. (1987). Optimal foraging and intraspecific diet differences in the lizard Cnemidophorus sexlineatus. Oecologia 71, 439–46.
Pease, C. M. and Bull, J. J. (1992). Is science logical?BioScience 42, 293–8.
Pereira, H. M., Bergman, A. and Roughgarden, J. (2003). Socially stable territories: the negotiation of space by interacting foragers. Am. Nat. 161, 143–52.
Perry, G. (1995). The evolutionary ecology of lizard foraging: a comparative study. Ph.D. dissertation, University of Texas at Austin.
Perry, G. (1996). The evolution of sexual dimorphism in the lizard Anolis polylepis (Iguania): evidence from intraspecific variation in foraging behavior and diet. Can. J. Zool. 74, 1238–45.
Perry, G. (1999). The evolution of search modes: ecological versus phylogenetic perspectives. Am. Nat. 153, 98–109.
Perry, G. and Brandeis, M. (1992). Variation in stomach contents of the gecko Ptyodactylus hasselquistii guttatus in relation to sex, age, season and locality. Amph.-Rept. 13, 275–82.
Perry, G. and Buden, D. W. (1999). Notes on the ecology, behavior and color variation of the green tree skink, Lamprolepis smaragdina (Lacertilia: Scincidae), in Micronesia. Micronesica 31, 263–73.
Perry, G. and Garland, T. Jr. (2002). Lizard home ranges revisited: effects of sex, body size, diet, habitat, and phylogeny. Ecology 83, 1870–85.
Perry, G. and Pianka, E. R. (1997). Foraging behaviour: past, present and future. Trends. Ecol. Evol. 12, 360–4.
Perry, G., Dmi'el, R. and Lazell, J. (1999). Evaporative water loss in insular populations of the Anolis cristatellus group (Reptilia: Sauria) in the British Virgin Islands II: the effects of drought. Biotropica 31, 337–43.
Perry, G., Dmi'el, R. and Lazell, J. (2000). Evaporative water loss in insular populations of Anolis cristatellus (Reptilia: Sauria) in the British Virgin Islands III: a common garden experiment. Biotropica 32, 722–8.
Perry, G., Lampl, I., Lerner, A.et al. (1990). Foraging mode in lacertid lizards: variation and correlates. Amph.-Rept. 11, 373–84.
Perry, G., LeVering, K., Girard, I. and Garland, T. Jr. (2004). Locomotor performance and social dominance in male Anolis cristatellus. Anim. Behav. 67, 37–47.
Pianka, E. R. (1966). Convexity, desert lizards, and spatial heterogeneity. Ecology 47, 1055–9.
Pianka, E. R. (1970). Comparative autecology of the lizard Cnemidophorus tigris in different parts of its geographic range. Ecology 51, 703–20.
Pianka, E. R. (1986). Ecology and Natural History of Desert Lizards. Princeton, NJ: Princeton University Press.
Pianka, E. R. (1993). The many dimensions of a lizard's ecological niche. In Lacertids of the Mediterranean Region, ed. Valakos, E. D., Böhme, W., Pérez-Mellado, V. and Maragou, P., pp. 121–54. Athens: Hellenic Zoological Society.
Pianka, E. R., Huey, R. B. and Lawlor, L. R. (1979). Niche segregation in desert lizards. In Analysis of Ecological Systems, ed. Horn, D. J., Stairs, R. and Mitchell, R. D., pp. 67–115. Columbus, OH: Ohio State University.
Rand, A. S., Dugan, B. A., Monteza, H. and Vianda, D. (1990). The diet of a generalized folivore: Iguana iguana in Panama. J. Herpetol. 24, 211–14.
Reagan, D. P. (1986). Foraging behavior of Anolis stratulus in a Puerto Rican rain forest. Biotropica 18, 157–60.
Reeder, T. W. (2003). A phylogeny of the Australian Sphenomorphus group (Scincidae: Squamata) and the phylogenetic placement of the crocodile skinks (Tribolonotus): A Bayesian approaches to assessing congruence and obtaining confidence in maximum likelihood inferred relationships. Molec. Phylog. Evol. 27, 384–97.
Reeder, T. W., Cole, C. J. and Dessauer, H. C. (2002). Phylogenetic relationships of whiptail lizards of the genus Cnemidophorus (Squamata: Teiidae): A test of monophyly, reevaluation of karyotypic evolution, and review of hybrid origins. Am. Mus. Nov. 3365, 1–61.
Regal, P. J. (1978). Behavioral differences between reptiles and mammals: an analysis of activity and mental capabilities. In Behavior and Neurology of Lizards, ed. Greenberg, N. and Maclean, P. D., pp. 183–202. Rockville, MD: NIMH.
Schwenk, K. (1995). Of tongues and noses: chemoreception in lizard and snakes. Trends. Ecol. Evol. 10, 7–12.
Shaffer, D. T. Jr. and Whitford, W. G. (1981) Behavioral responses of a predator, the round-tailed horned lizard, Phrynosoma modestum and its prey, honey pot ants, Myrmecocystus spp. Am. Midl. Nat. 105, 209–16.
Sih, A., Bell, A. M., Johnson, J. C. and Ziemba, R. E. (2004). Behavioral syndromes: an integrative overview. Quart. Rev. Biol. 79, 241–77.
Sokal, R. R. and Rohlf, F. J. (1995). Biometry, 3rd edn. New York: Freeman.
Stephens, D. W. and Krebs, J. R. (1986). Foraging Theory. Princeton, NJ: Princeton University Press.
Sugarman, R. A. and Hacker, R. A. (1980). Observer effects on collared lizards. J. Herpetol. 14, 188–90.
Taylor, J. A. (1986). Food and foraging behavior of the lizard, Ctenotus taeniolatus. Australian J. Ecol. 11, 49–54.
Travers, S. E. and Sih, A. (1991). The influence of starvation and predators on the mating behavior of a semiaquatic insect. Ecology 72, 2123–36.
Turner, F. B. and Medica, P. A. (1982). The distribution and abundance of the flat-tailed horned lizard (Phrynosoma mcallii). Copeia 1982, 815–23.
Vitt, L. J., Zani, P. A., Caldwell, J. C. and Durtsche, R. D. (1993). Ecology of the whiptail lizard Cnemidophorus deppii on a tropical beach. Can. J. Zool. 71, 2391–400.
Weiner, J. (1995). On the practice of ecology. J. Ecol. 83, 153–8.
Weinstein, R. B. and Full, R. J. (1999). Intermittent locomotion increases endurance in a gecko. Physiol. Biochem. Zool. 72, 732–9.
Werner, Y. L. and Chou, L. M. (2002). Observations on the ecology of the arrhythmic equatorial gecko Cnemaspis kendallii in Singapore (Sauria: Gekkoninae). Raffles Bull. Zool. 50, 185–96.
Werner, Y. L., Okada, S., Ota, H., Perry, G. and Tokunaga, S. (1997). Varied and fluctuating foraging modes in nocturnal lizards of the family Gekkonidae. Asia. Herpetol. Res. 7, 153–65.
Wiens, J. J., Reeder, T. W. and Oca, A. N. M. (1999). Molecular phylogenetics and evolution of sexual dichromatism among populations of the Yarrow's spiny lizard (Sceloporus jarrovii). Evolution 53, 1884–97.
Wymann, M. N. and Whiting, M. J. (2002). Foraging ecology of rainbow skinks (Mabuya margaritifer) in southern Africa. Copeia 2002, 943–57.