Journal Articles: 2001-1999

Journal Article
A. K. Knox, J. B. Losos, and C. J. Schneider. 2001. “Adaptive radiation versus intraspecific differentiation: morphological variation in Caribbean Anolis lizards.” Journal of Evolutionary Biology, 14, Pp. 904-909. PDF
C. J. Schneider, J. B. Losos, and Kevin de Queiroz. 2001. “Evolutionary relationships of Anolis bimaculatus group from the northern Lesser Antilles.” Journal of Herpetology, 35, Pp. 1-12.
D. A. Creer, K. de Queiroz, T. R. Jackman, J. B. Losos, and A. Larson. 2001. “Systematics of the Anoils request series of the southern Lesser Antilles.” Journal of Herpetology, 35, Pp. 428-441.
T. W. Schoener, D. A. Spiller, and J. B. Losos. 2001. “Natural restoration of the species-area relation for a lizard after a hurricane.” Science, 294, Pp. 1525-8.Abstract

We document the decimation and recovery of the commonest lizard species, Anolis sagrei, on 66 islands in the Bahamas that were directly hit by Hurricane Floyd in September 1999. Before the hurricane, an island's area was a better predictor of the occurrence of A. sagrei than was its altitude. Immediately after, altitude was a better predictor: Apparently all lizards on islands lower than about 3 meters maximum elevation perished in the storm surge. After about 1 year, area again became the better predictor. By 19 months after the hurricane, A. sagrei populations occurred on 88% of the islands they formerly occupied. Recovery occurred via overwater colonization and propagation from eggs that survived inundation, mechanisms that were enhanced by larger island area. Thus, natural processes first destroyed and then quickly restored a highly regular species-area distribution.

T. W. Schoener, D. A. Spiller, and J. B. Losos. 2001. “Predators increase the risk of catastrophic extinction of prey populations.” Nature, 412, Pp. 183-6.Abstract

There has been considerable research on both top-down effects and on disturbances in ecological communities; however, the interaction between the two, when the disturbance is catastrophic, has rarely been examined. Predators may increase the probability of prey extinction resulting from a catastrophic disturbance both by reducing prey population size and by changing ecological traits of prey individuals such as habitat characteristics in a way that increases the vulnerability of prey species to extinction. We show that a major hurricane in the Bahamas led to the extinction of lizard populations on most islands onto which a predator had been experimentally introduced, whereas no populations became extinct on control islands. Before the hurricane, the predator had reduced prey populations to about half of those on control islands. Two months after the hurricane, we found only recently hatched individuals--apparently lizards survived the inundating storm surge only as eggs. On predator-introduction islands, those hatchling populations were a smaller fraction of pre-hurricane populations than on control islands. Egg survival allowed rapid recovery of prey populations to pre-hurricane levels on all control islands but on only a third of predator-introduction islands--the other two-thirds lost their prey populations. Thus climatic disturbance compounded by predation brought prey populations to extinction.

J. B. Losos, T. W. Schoener, KI Warheit, and D. Creer. 2001. “Experimental studies of adaptive differentiation in Bahamian Anolis lizards.” Genetica, 112-113, Pp. 399-415.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.

M. Leal and J. B. Losos. 2000. “Natural history of the Cuban lizard (Chamaeleolis barbatus).” Journal of Herpetology, 34, Pp. 318-322. PDF
J. B. Losos, D. A. Creer, D. Glossip, R. Goellner, A. Hampton, G. Roberts, N. Haskell, P. Taylor, and J. Ettling. 2000. “Evolutionary implications of phenotypic plasticity in the hindlimb of the lizard Anolis sagrei.” Evolution, 54, Pp. 301-5.Abstract

Species of Anolis lizards that use broad substrates have long legs, which provide enhanced maximal sprint speed, whereas species that use narrow surfaces have short legs, which permit careful movements. We raised hatchling A. sagrei in terraria provided with only broad or only narrow surfaces. At the end of the experiment, lizards in the broad treatment had relatively longer hindlimbs than lizards in the narrow treatment. These results indicate that not only is hindlimb length a plastic trait in these lizards, but that this plasticity leads to the production of phenotypes appropriate to particular environments. Comparison to hindlimb lengths of other Anolis species indicates that the range of plasticity is limited compared to the diversity shown throughout the anole radiation. Nonetheless, this plasticity potentially could have played an important role in the early stages of the Caribbean anole radiation.

M. A. Butler, T. W. Schoener, and J. B. Losos. 2000. “The relationship between sexual size dimorphism and habitat use in Greater Antillean Anolis lizards.” Evolution, 54, Pp. 259-72.Abstract

Sexual size dimorphism (SSD) is the evolutionary result of selection operating differently on the body sizes of males and females. Anolis lizard species of the Greater Antilles have been classified into ecomorph classes, largely on the basis of their structural habitat (perch height and diameter). We show that the major ecomorph classes differ in degree of SSD. At least two SSD classes are supported: high SSD (trunk-crown, trunk-ground) and low SSD (trunk, crown-giant, grass-bush, twig). Differences cannot be attributed to an allometric increase of SSD with body size or to a phylogenetic effect. A third explanation, that selective pressures on male and/or female body size vary among habitat types, is examined by evaluating expectations from the major relevant kinds of selective pressures. Although no one kind of selective pressure produces expectations consistent with all of the information, competition with respect to structural habitat and sexual selection pressures are more likely possibilities than competition with respect to prey size or optimal feeding pressures. The existence of habitat-specific sexual dimorphism suggests that adaptation of Anolis species to their environment is more complex than previously appreciated.

J. B. Losos and D. Schluter. 2000. “Analysis of an evolutionary species-area relationship.” Nature, 408, Pp. 847-50.Abstract

Large islands typically have more species than comparable smaller islands. Ecological theories, the most influential being the equilibrium theory of island biogeography, explain the species-area relationship as the outcome of the effect of area on immigration and extinction rates. However, these theories do not apply to taxa on land masses, including continents and large islands, that generate most of their species in situ. In this case, species-area relationships should be driven by higher speciation rates in larger areas, a theory that has never been quantitatively tested. Here we show that Anolis lizards on Caribbean islands meet several expectations of the evolutionary theory. Within-island speciation exceeds immigration as a source of new species on all islands larger than 3,000 km2, whereas speciation is rare on smaller islands. Above this threshold island size, the rate of species proliferation increases with island area, a process that results principally from the positive effects of area on speciation rate. Also as expected, the slope of the species-area relationship jumps sharply above the threshold. Although Anolis lizards have been present on large Caribbean islands for over 30 million years, there are indications that the current number of species still falls below the speciation-extinction equilibrium.

J. B. Losos and D. Spiller. 1999. “Differential colonization success and asymmetrical interactions between two lizard species.” Ecology, 80, Pp. 252-258. PDF
K. Beuttell and J. B. Losos. 1999. “Ecological morphology of Caribbean anoles.” Herpetological Monographs, 13, Pp. 1-28. PDF
KI Warheit, J.D. Forman, J. B. Losos, and D. B. Miles. 1999. “Morphological diversification and adaptive radiation: a comparison of two diverse lizards clades.” Evolution, 53, Pp. 1226-1234. PDF
T. R. Jackman, A. Larson, K. de Queiroz, and J. B. Losos. 1999. “Phylogenetic relationships and the tempo of early diversification in Anolis lizards.” Systematic Biology, 48, Pp. 254-285. PDF
D. J. Irschick and 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.” Am Nat, 154, Pp. 293-305.Abstract

Recent years have seen an increased emphasis on measuring ecologically relevant performance capabilities to understand associations between morphology and habitat use. Such studies presume that performance is invariant, but in eight Caribbean Anolis lizard species, we found that maximal sprinting ability depends on surface diameter. Moreover, these species differ in the degree to which sprint speed declines with decreasing surface diameter, defined as "sprint sensitivity" (high sprint sensitivity=substantial declines in speed between broad and narrow dowels). The habitat constraint hypothesis postulates that Anolis lizards will avoid structural habitats in which their maximal sprinting capabilities are impaired. The habitat breadth hypothesis postulates that species whose performance is less affected by substrate will use a greater variety of habitats than species whose performance varies to a greater extent on surfaces of different diameters. Field observations quantified the proportion of time that lizards spent on different perch diameters. Both hypotheses were confirmed: species with high values of sprint sensitivity avoided using perches on which their maximal sprinting abilities are impaired, whereas species with low sprint sensitivity used such "submaximal" surfaces more frequently. Species with low sprint sensitivity used a broader range of structural habitats than species with high sprint sensitivity.

J. B. Losos. 1999. “Uncertainty in the reconstruction of ancestral character states and limitations on the use of phylogenetic comparative methods.” Anim Behav, 58, Pp. 1319-1324. PDF