Skip to main content

Experimental studies of adaptive differentiation in Bahamian Anolis lizards

  • Chapter
Microevolution Rate, Pattern, Process

Part of the book series: Contemporary Issues in Genetics and Evolution ((CIGE,volume 8))

Abstract

Populations of the lizards Anolis carolinensis and A. sagrei were experimentally introduced onto small islands in the Bahamas. Less than 15 years after introduction, we investigated whether the populations had diverged and, if so, whether differentiation was related to island vegetational characteristics or propagule size. No effect of founding population size was evident, but differentiation of A. sagrei appears to have been adaptive, a direct relationship existed between how vegetationally different an experimental island was from the source island and how much the experimental population on that island had diverged morphologically. Populations of A. carolinensis had also diverged, but were too few for quantitative comparisons. A parallel exists between the divergence of experimental populations of A. sagrei and the adaptive radiation of Anolis lizards in the Greater Antilles; in both cases, relative hindlimb length and perch diameter are strongly correlated. This differentiation could have resulted from genetic change or environmentally-driven phenotypic plasticity. Laboratory studies on A. sagrei from a population in Florida indicate that hindlimb length exhibits adaptive phenotypic plasticity. Further studies are required to determine if the observed differences among the experimental populations are the result of such plasticity. Regardless of whether the differences result from plasticity, genetic change, or both, the observation that anole populations differentiate rapidly and adaptively when exposed to novel environmental conditions has important implications for understanding the adaptive radiation of Caribbean anoles.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 169.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 219.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 219.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Ashton, E.H. & S. Zuckerman, 1951. The influence of geographic isolation on the skull of the green monkey (Cercopithecus ae-thiops sabaeus): II. the cranial dimensions of the St. Kitts and the African green monkey. Proc. R. Soc. Lond. 138: 204–212.

    Article  CAS  PubMed  Google Scholar 

  • Autumn, K., Y.A. Liang, S. T. Hsieh, W. Zeach, W.P. Chan, T.W. Kenny, R. Fearing & R.J. Full, 2000. Adhesive force of a single gecko foot-hair. Nature 405: 681–685.

    Article  CAS  PubMed  Google Scholar 

  • Baker, A.J., 1980. Morphometric differentiation in New Zealand populations of the house sparrow (Passer domesticus). Evolution 34: 638–653.

    Article  Google Scholar 

  • Baker, A.J. & A. Moeed, 1979. Evolution in the introduced New Zealand populations of the common myna, Acridotheres tristis (Aves: Sturnidae). Can. J. Zool. 57: 570–584.

    Article  Google Scholar 

  • Barton, N.H., 1989. Founder effect speciation, pp. 229–256 in Spe-ciation and its Consequences, edited by D. Otte & J.A. Endler. Sinauer Assoc, Sunderland, MA.

    Google Scholar 

  • Barton, N.H., 1996. Natural selection and random genetic drift as causes of evolution on islands. Phil. Trans. Royal Soc. Lond. 351: 785–795.

    Article  CAS  Google Scholar 

  • Barton, N.H. & B. Charlesworth, 1984. Genetic revolutions, founder effects, and speciation. Ann. Rev. Ecol. Syst. 15: 133–164.

    Article  Google Scholar 

  • Bernays, E.A., 1986. Diet-induced head allometry among foliage-chewing insects and its importance for graminivores. Science 231: 495–497.

    Article  CAS  PubMed  Google Scholar 

  • Berry, R.J., 1964. The evolution of an island population of the house mouse. Evolution 18: 468–483.

    Article  Google Scholar 

  • Beutteil, K. & J.B. Losos, 1999. Ecological morphology of Caribbean anoles. Herpetol. Monogr. 13: 1–28.

    Article  Google Scholar 

  • Bookstein, F.L., 1989. ’size and shape’: a comment on semantics. Syst. Zool. 38: 173–180.

    Article  Google Scholar 

  • Booth, F.W. & E.W. Gould, 1975. Effects of training and disuse on connective tissue, pp. 83–112 in Exercise and Sports Sciences Reviews, Vol. 3, edited by J.H. Wilmore & J.F. Keogh. Academic Press, New York.

    Google Scholar 

  • Bryant, E.H. & L.M. Meffert, 1993. The effect of a serial founder-flush cycles on quantitative genetic variation in the housefly. Heredity 70: 122–129.

    Article  Google Scholar 

  • Bryant, E.H. & L.M. Meffert, 1996. Morphometric differentiation in serially bottlenecked populations of the housefly. Evolution 50: 935–940.

    Article  Google Scholar 

  • Burnaby, T.P., 1966. Growth-invariant discriminant functions and generalized distances. Biometrics 22: 96–110.

    Article  Google Scholar 

  • Buskirk, E.R., K.L. Andersen & J. Brozek. 1956. Unilateral activity and bone and muscle development in the forearm. Res. Quart. Amer. Assoc. Health Phys. Educ. 27: 127–131.

    Google Scholar 

  • Carlquist, S., 1974. Island Biology. Columbia Univ. Press, New York.

    Google Scholar 

  • Carroll, S.P. & C. Boyd, 1992. Host race radiation in the soapberry bug: natural history with the history. Evolution 46: 1052–1069.

    Article  Google Scholar 

  • Carson, H.L. & A.R. Templeton, 1984. Genetic revolutions in relation to speciation phenomena: the founding of new populations. Ann. Rev. Ecol. Syst. 15: 97–131.

    Article  Google Scholar 

  • Cheverud, J.M. & E.J. Routman, 1996. Epistasis as a source of increased additive genetic variance at population bottlenecks. Evolution 50: 1042–1051.

    Article  Google Scholar 

  • Cheverud, J.M., T.T. Vaughn, L.S. Pletscher, K. King-Ellison, J. Bailiff, E. Adams, C. Erickson & A. Bonislawski, 1999. Epistasis and the evolution of additive genetic variance in populations that pass through a bottleneck. Evolution 53: 1009–1018.

    Article  Google Scholar 

  • Coker, W.C., 1905. Vegetation of the Bahama Islands, pp. 185–270 in The Bahama Islands, edited by G.B. Shattuck. Macmillan, New York.

    Google Scholar 

  • Conant, S., 1988. Geographic variation in the Laysan finch (Telespyza cantans). E vol. Ecol. 2: 270–282.

    Google Scholar 

  • Erickson, G.M., 1997. The Evolution of the Biomechanical Attributes of Long Bones. Ph.D. Dissertation, University of California. Berkeley.

    Google Scholar 

  • Fox, W., 1963. Special tubules for sperm storage in female lizards. Nature 198: 500–501.

    Article  Google Scholar 

  • Frankel, O.H. & M.E. Soule, 1981. Conservation and Evolution. Cambridge Univ. Press. Cambridge.

    Google Scholar 

  • Frankham, R., K. Lees, M.E. Montgomery, PR. England, E.H. Lowe & D.A. Briscoe, 1999. Do population size bottlenecks reduce evolutionary potential? Anim. Cons. 2: 25–260.

    Google Scholar 

  • Franklin, I.R., 1980. Evolutionary change in small populations, pp. 135–149 in Conservation Biology: An Evolutionary-Ecological Perspective, edited by M.E. Soule & B.A. Wilcox. Sinauer Associates, Sunderland, Ma.

    Google Scholar 

  • Gilpin, M.E. & M.E. Soulé. 1986. Minimum viable populations: processes of species extinction, pp. 19–34 in Conservation Biology: the Science of Scarcity and Diversity, edited by M.E. Soulé. Sinauer Associates, Sunderland, Ma.

    Google Scholar 

  • Gingerich, P.D., 1983. Rates of evolution: effects of time and temporal scaling. Science 222: 159–161.

    Article  CAS  PubMed  Google Scholar 

  • Glossip, D. & J.B. Losos, 1997. Ecological correlates of number of subdigital lamellae in anoles. Herpetologica 53: 192–199.

    Google Scholar 

  • Goodnight, C.J., 1987. On the effect of founder events on epistatic genetic variance. Evolution 41: 80–91.

    Article  Google Scholar 

  • Hendry, A.P. & M. T. Kinnison, 1999. The pace of modern life: measuring rates of contemporary microevolution. Evolution 53: 1637–1653.

    Article  Google Scholar 

  • Huxley, J., 1942. Evolution: The Modern Synthesis. Harper & Bros., New York, 645 pp.

    Google Scholar 

  • Irschick, D.J. & J.B. Losos, 1998. A comparative analysis of the ecological significance of maximal locomotor performance in Caribbean Anolis lizards. Evolution 52: 219–226.

    Article  Google Scholar 

  • Irschick, D.J. & J.B. Losos, 1999. Do lizards avoid habitats in which performance is submaximal?: The relationship between sprinting capabilities and structural habitat use in Caribbean anoles. Amer. Natural. 154: 293–305.

    Article  Google Scholar 

  • James, F.C., 1983. Environmental component of morphological differentiation in birds. Science 221: 184–187.

    Article  CAS  PubMed  Google Scholar 

  • James, F.C., 1991. Complementary descriptive and experimental studies of clinal variation in birds. Amer. Zool. 31: 694–706.

    Google Scholar 

  • Johnston, R., 1992. Evolution in the rock dove: skeletal morphology. Auk 109: 530–542.

    Google Scholar 

  • Johnston, R.F. & R.K. Selander, 1971. Evolution in the house sparrow. II. Adaptive differentiation in North American populations. Evolution 25: 1–28.

    Article  Google Scholar 

  • Jones, H.H., J.D. Priest, W.C. Hayes, C.C. Tichenor & D.A. Nagel, 1977. Humeral hypertrophy in response to exercise. J. Bone Joint Surg. 59-A: 204–208.

    Google Scholar 

  • Kato, S. & T. Ishiko, 1966. Obstructed growth of children’s bones due to excessive labor in remote corners, p. 479 in Proc. Int. Congress Sport Sci., edited by K. Kato. Japanese Union of Sport Sciences, Tokyo.

    Google Scholar 

  • Kiiskinen, A., 1977. Physical training and connective tissues in young mice — physical properties of achilles tendons and long bones. Growth 41: 123–137.

    CAS  PubMed  Google Scholar 

  • Kinnison, M.T. & A.P. Hendry, 2001. The pace of modern life. II: from rates to pattern and process. Genetica 112-113: 145–164.

    Article  CAS  PubMed  Google Scholar 

  • Lints, F.A. & M. Bourgois, 1982. A test of the genetic revolution hypothesis of speciation, pp. 423–436 in Advances in Genetics, Development, and Evolution of Drosophila, edited by S. Lakovaara. Plenum Press, NY.

    Chapter  Google Scholar 

  • Loitz, B.J. & R.F. Zernicke, 1992. Strenuous exercise-induced remodelling of mature bone: relationships between in vivo strains and bone mechanics. J. Exp. Biol. 170: 1–18.

    CAS  PubMed  Google Scholar 

  • Losos, J.B., 1990a. The evolution of form and function: morphology and locomotor performance in West Indian Anolis lizards. Evolution 44: 1189–1203.

    Article  Google Scholar 

  • Losos, J.B., 1990b. Ecomorphology, performance capability, and scaling of West Indian Anolis lizards: an evolutionary analysis. Ecol. Mon. 60: 369–388.

    Article  Google Scholar 

  • Losos, J.B., D.A. Creer, D. Glossip, R. Goellner, A. Hampton, G. Roberts, N. Haskell, P. Taylor & J. Etling. 2000. Evolutionary implications of phenotypic plasticity in the Hindlimb of the lizard Anolis sagrei. Evolution 54: 301–305.

    CAS  PubMed  Google Scholar 

  • Losos, J.B. & D.J. Irschick. 1996. The effect of perch diameter on escape behaviour of Anolis lizards: laboratory-based predictions and field tests. Anim. Behav. 51: 593–602.

    Article  Google Scholar 

  • Losos, J.B., D.J. Irschick & T.W. Schoener, 1994. Adaptation and constraint in the evolution of specialization of Bahamian Anolis lizards. Evolution 48: 1786–1798.

    Article  Google Scholar 

  • Losos, J.B., T.R. Jackman, A. Larson, K. de Queiroz & L. Rodríguez-Schettino, 1998. Historical contingency and determinism in replicated adaptive radiations of island lizards. Science 279: 2115–2118.

    Article  CAS  PubMed  Google Scholar 

  • Losos, J.B. & B. Sinervo, 1989. The effect of morphology and perch diameter on sprint performance of Anolis lizards. J. Exp. Biol. 145: 23–30.

    Google Scholar 

  • Losos, J.B., K.I. Warheit & T.W. Schoener, 1997. Adaptive differentiation following experimental island colonization in Anolis lizards. Nature 387: 70–73.

    Article  CAS  Google Scholar 

  • Manly, B.F.J., 1991. Randomization and Monte Carlo Methods in Biology. Chapman & Hall, London.

    Book  Google Scholar 

  • Mayer, G.C., 1989. Deterministic patterns of community structure in West Indian reptiles and amphibians. Ph.D. Dissertation, Harvard University.

    Google Scholar 

  • Mayr, E., 1963. Animal Species and Evolution. Belknap Press, Cambridge, MA.

    Google Scholar 

  • Meyer, A. 1987. Phenotypic plasticity and heterochrony in Cichla-soma managuense (Pisces, Cichlidae) and their implications for speciation in cichlid fishes. Evolution 41: 1357–1369.

    Article  Google Scholar 

  • Nei, M., T. Maruyama & R. Chakraborty, 1975. The bottleneck effect and genetic variability in populations. Evolution 29: 1–10 The bottleneck effect and genetic variability in populations. Evolution 29: 1–10.

    Article  Google Scholar 

  • Neter, J., W. Wasserman & M.H. Kutner, 1985. Applied Linear Statistical Models: Regression, Analysis of Variance, and Experimental Design. R.D. Irwin, Homewood, II., 2nd edn.

    Google Scholar 

  • Patton, J.L. & P.V. Brylski, 1988. Pocket gophers in alfalfa fields: causes and consequences of habitat-related body size variation. Am. Nat. 130: 493–506.

    Article  Google Scholar 

  • Rand, A.S., 1964. Ecological distribution in anoline lizards of Puerto Rico. Ecology 45: 745–752.

    Article  Google Scholar 

  • Rand, A.S. & E. E. Williams, 1969. The anoles of La Palma. Breviora 327: 1–19.

    Google Scholar 

  • Reznick, D.N. & Ghalamboor, 2001.

    Google Scholar 

  • Reznick, D.N., F.H. Shaw, F.H. Rodd & R.G. Shaw, 1997. Evaluation of the rate of evolution in natural populations of guppies (Poecilia reticulata). Science 275: 1934–1937.

    Article  CAS  PubMed  Google Scholar 

  • Rhymer, J.M., 1992. An experimental study of geographic variation in avian growth and development. J. Evol. Biol. 5: 289–306.

    Article  Google Scholar 

  • Rice, W.R. & E.E. Hostert, 1993. Perspective: laboratory experiments on speciation: what have we learned in forty years? Evolution 47: 1637–1653.

    Article  Google Scholar 

  • Roughgarden, J.D. & E. Fuentes, 1977. The environmental determinants of size in solitary populations of West Indian Anolis lizards. Oikos 29: 44–51.

    Article  Google Scholar 

  • Rundle, H.D., A.O. Mooers & M.C. Whitlock, 1998. Single founder-flush events and the evolution of reproductive isolation. Evolution 52: 1850–1855.

    Article  Google Scholar 

  • Rundle, H.D., A.O. Mooers & M.C. Whitlock, 1999. Experimental tests of founder-flush: a reply to Templeton. Evolution 53: 1632–1633.

    Article  Google Scholar 

  • Schlichting, C.D. & M. Pigliucci, 1998. Phenotypic Evolution: A Reaction Norm Perspective. Sinauer Publ., Sinauer, MA.

    Google Scholar 

  • Schmalhausen, I.I., 1949. Factors of Evolution. Blakiston, Philadelphia.

    Google Scholar 

  • Schoener, T.W., 1968. The Anolis lizards of Bimini: resource partitioning in a complex fauna. Ecology 49: 704–726.

    Article  Google Scholar 

  • Schoener, T.W., 1986. Patterns in terrestrial vertebrate versus arthropod communities: do systematic differences in regularity exist, pp. 556–586 in Community Ecology, edited by J. Diamond & T.J. Case. Harper & Row, New York.

    Google Scholar 

  • Schoener, T.W. & A. Schoener, 1978. Inverse relation of survival of lizards with island size and avifaunal richness. Nature 274: 685–687.

    Article  Google Scholar 

  • Schoener, T.W. & A. Schoener, 1980. Densities, sex ratios, and population structure in four species of Bahamian Anolis lizards. J. Anim. Ecol. 49: 19–53.

    Article  Google Scholar 

  • Schoener, T.W. & A. Schoener, 1983. The time to extinction of a colonizing propagule of lizards increases with island area. Nature 302: 332–334.

    Article  Google Scholar 

  • Simpson, G.G., 1953. The Baldwin effect. Evolution 7: 110–117.

    Article  Google Scholar 

  • Sinervo, B. & J.B. Losos, 1991. Walking the tight rope: arboreal sprint performance among Sceloporus occidentalis lizard populations. Ecology 72: 1225–1233.

    Article  Google Scholar 

  • Sokal, R.R. & F.J. Rohlf, 1995. Biometry. W.H. Freeman & Co., New York.

    Google Scholar 

  • Spiller, D.A., J.B. Losos & T.W. Schoener, 1998. Impact of a catastrophic hurricane on island populations. Science 281: 695–697.

    Article  CAS  PubMed  Google Scholar 

  • St. Louis, V.L. & J.C. Barlow, 1991. Morphometric analyses of introduced and ancestral populations of the Eurasian tree sparrow. Wilson Bull. 103: 1–12.

    Google Scholar 

  • Stamps, J.A., 1993. Sexual size dimorphism in species with asymptotic growth after maturity. Biol. J. Linn. Soc. 50: 123–145.

    Article  Google Scholar 

  • Stamps, J.A., V.V. Krishnan & R.M. Andrews, 1994. Analyses of sexual size dimoiphism using null growth-based models. Copeia 1994: 598–613.

    Article  Google Scholar 

  • Steinhaus, A.H., 1933. Chronic effects of exercise. Physiol. Rev. 13: 103–147.

    Google Scholar 

  • Sultan, S.E., 1987. Evolutionary implications of phenotypic plasticity in plants. Evol. Biol. 21: 127–178.

    Google Scholar 

  • Templeton, A.R., 1980. The theory of speciation via the founder principle. Genetics 94: 1011–1038.

    CAS  PubMed Central  PubMed  Google Scholar 

  • Templeton, A.R., 1996. Experimental evidence for the genetic-transilience model of speciation. Evolution 50: 909–915.

    Article  Google Scholar 

  • Templeton, A.R., 1999. Experimental tests of genetic transiliencc. Evolution 53: 1628–1632.

    Article  Google Scholar 

  • Trassell, G.C. & R.J. Etter, 2001. Integrating genetic and environmental forces that shape the evolution of geographic variation. Genetica.

    Google Scholar 

  • Waddington, C.H., 1975. The Evolution of an Evolutionist. Cornell University Press, Ithaca.

    Google Scholar 

  • West-Eberhard, M. J., 1989. Phenotypic plasticity and the origins of diversity. Ann. Rev. Ecol. Syst. 20: 249–278.

    Article  Google Scholar 

  • Williams, E.E., 1983. Ecomorphs, faunas, island size, and diverse end points in island radiations of Anolis, pp. 326–370 in Lizard Ecology: Studies of a Model Organism, edited by R.B. Huey, E.R. Pianka & T.W. Schoener. Harvard University Press, Cambridge.

    Google Scholar 

  • Woo, S.L.-Y., S.C. Kuei, D. Amiel, M.A. Gomez, W.C. Hayes, F.C. White & W.H. Akeson, 1981. The effect of prolonged physical training on the properties of long bone: a study of Wolff’s Law. J. Bone Joint Surg. 63-A: 780–786.

    Google Scholar 

  • Wright, S., 1977. Evolution and the genetics of populations, in Experimental Results and Evolutionary Deductions. Vol. 3. University of Chicago Press, Chicago.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

A. P. Hendry M. T. Kinnison

Rights and permissions

Reprints and permissions

Copyright information

© 2001 Springer Science+Business Media Dordrecht

About this chapter

Cite this chapter

Losos, J.B., Schoener, T.W., Warheit, K.I., Creer, D. (2001). Experimental studies of adaptive differentiation in Bahamian Anolis lizards. In: Hendry, A.P., Kinnison, M.T. (eds) Microevolution Rate, Pattern, Process. Contemporary Issues in Genetics and Evolution, vol 8. Springer, Dordrecht. https://doi.org/10.1007/978-94-010-0585-2_24

Download citation

  • DOI: https://doi.org/10.1007/978-94-010-0585-2_24

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-3889-8

  • Online ISBN: 978-94-010-0585-2

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics