Most studies interpret reptilian sexual size dimorphism (SSD) as a means to reducing resource competition by way of sexual selection, fecundity selection, and natural selection. This chapter assesses the importance of these processes using data on 832 species of snakes, lizards, and turtles. The data reveal allometry consistent with Rensch's rule in most, but not all reptilian taxa, and support the hypothesis that sexual selection for large male size has influenced the evolution of reptile SSD. However, more data on male combat and territoriality are needed to test more fully this hypothesis. Although fecundity increases with female body size in many reptiles, comparative data provide only weak support for the fecundity advantage of large female size. The chapter concludes that further progress in assessing the relative importance of different selective processes in reptiles will require studies that more fully integrate evolutionary hypotheses with knowledge of proximate physiological and developmental mechanisms.
Phylogenetic comparative analysis is an approach to inferring evolutionary process from a combination of phylogenetic and phenotypic data. The last few years have seen increasingly sophisticated models employed in the evaluation of more and more detailed evolutionary hypotheses, including adaptive hypotheses with multiple selective optima and hypotheses with rate variation within and across lineages. The statistical performance of these sophisticated models has received relatively little systematic attention, however. We conducted an extensive simulation study to quantify the statistical properties of a class of models toward the simpler end of the spectrum that model phenotypic evolution using Ornstein–Uhlenbeck processes. We focused on identifying where, how, and why these methods break down so that users can apply them with greater understanding of their strengths and weaknesses. Our analysis identifies three key determinants of performance: a discriminability ratio, a signal-to-noise ratio, and the number of taxa sampled. Interestingly, we find that model-selection power can be high even in regions that were previously thought to be difficult, such as when tree size is small. On the other hand, we find that model parameters are in many circumstances difficult to estimate accurately, indicating a relative paucity of information in the data relative to these parameters. Nevertheless, we note that accurate model selection is often possible when parameters are only weakly identified. Our results have implications for more sophisticated methods inasmuch as the latter are generalizations of the case we study.
Despite its role in whole-animal performance, the adaptation of muscle physiology related to terrestrial locomotion remains underexplored. We tested evolutionary models based on predator escape and foraging strategies of lizards to assess whether fiber-type composition of a leg muscle is adaptive for behavior. The best-fitting model for fast-twitch fiber-type evolution was one based on predator-escape strategy, while the foraging-mode model fared poorly (Akaike Information Criterion with small sample size correction; DeltaAICc=29.7). According to the predator-escape model, lizards relying on sprints to avoid predators are predicted to have relatively higher proportions of fast glycolytic (FG) fibers (70%), while cryptic lizards are predicted to have relatively higher fast oxidative glycolytic (FOG) fiber proportions (77%). This pattern suggests an evolutionary trend toward greater FG (FOG) fiber composition among lizards that specialize in sprinting (crypsis). The best-fitting model for slow-twitch fibers had a single optimum, suggesting a common selective pressure across these lizards. The second-best model explaining slow-twitch fiber-type evolution was Brownian motion (DeltaAICc=0.80), indicating some support for neutral evolution. We find evidence suggesting that different fiber types occurring in the same muscle can evolve under different evolutionary pressures.
— 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.
21 March 2005 in Biological Journal of the Linnean Society
Foraging mode is an important aspect of life history, often associated with traits such as locomotor mode, energy budget, risk of predation and reproductive effort. Because of these life-history associations, classification of foraging mode can be conceptually useful. Lizards figured prominently in the historical development of foraging mode concepts, yet our current understanding is dominated by only two lizard families which are good examples of the two extreme modes, sit-and-wait vs. active foraging. A great deal of lizard phylogenetic diversity remains unrepresented. Chameleons are a highly derived lizard taxon for which we have very little behavioural or ecological data, and no foraging mode data. Because chameleons are so unusual, it is not possible to predict where they will fit within the bimodal paradigm. I studied time budget and foraging mode in the Cape dwarf chameleon, Bradypodion pumilum, in Stellenbosch, South Africa. Several approaches were taken to assess foraging behaviour. First, lag-sequential analysis was applied to compare rates behaviours associated with observed eating events, which did not support a sit-and-wait foraging mode. Second, the number of moves per minute (MPM) and per cent time moving (%TM) were compared with those of other lizard taxa from the literature. Foraging in B. pumilum was found to be most consistent with an active foraging mode, although the MPM is unusually low. Thus I propose classification of B. pumilum as a cruise forager. Sufficient data are available to define a discriminant function for active vs. sit-and-wait modes among lizard speries, which classifys B. pumilum as active and additionally lends statistical support for good separation between foraging modes. These findings are discussed in relation to the evolution of foraging modes in chameleons and other lizard families.