Phenotypic plasticity is an environmentally based change in phenotype and can be adaptive. Often, the change in an organism's phenotype is induced by the presence of a predator and serves as a defense against that predator. Defensive phenotypes are induced in freshwater physid snails in response to both crayfish and molluscivorous fish. Alternative morphologies are produced depending on which of these two predators snails are raised with, thus protecting them from each of these predators' unique mode of predation. Snails and other mollusks have been shown to produce thicker, differently shaped shells when found with predators relative to those found without predators. This production of thicker, differently shaped shells offers better protection against predators because of increased predator resistance. The first study in this thesis explores costs and limits to plasticity using the snailfish- crayfish system. I exposed juvenile physid snails (using a family structure) to either early or late shifts in predation regimes to assess whether developmental flexibility is equally possible early and late in development. Physid snails were observed to produce alternative defensive morphologies when raised in the presence of each of the two predators. All families responded similarly to the environment in which they were raised. Morphology was found to be heritable, but plasticity itself was not heritable. Morphology was found to become less flexible as snails progressed along their respective developmental pathways. In the second study, I raised physid snails with and without shell-crushing sunfish and examined the differences in shell thickness, shell mass, shell size and shell microstructural properties between the two treatment groups. Shells of snails raised with predators were found to be larger, thicker and more massive than those raised without predators, but differences in microstructure were found to be insignificant. I conclude that the observed shell thickening is accomplished by the snails' depositing more of the same material into their shells and not by producing a more complex shell composition.

Characters of scale surface microstructure are combined with 'traditional' morphological characters in a phylogenetic analysis of the Tropidurini. Tropidurid lizards show variation in types of coarse and fine scale surface microstructure, in the anatomical distribution of different scale surface features, and in scale organ morphology and distribution. The morphology of the inner surface zone of scales is here described for the first time using scanning electron microscopy. Our phylogeny differs considerably from those proposed in earlier studies. New characters and frequency coding of polymorphic characters help resolve the problematic relationships of several species. Statistical confidence supports recognition ot one large cis-Andean and one large trans-Andean clade of species. Based on our results, we synonymize Plesiomicrolophus with Microlophus and Uranoscodon with Tropidurus. The phylogenetic relationships of newly discovered Tropidurus are resolved: T. callathelys is the sister species of T. melanopleurus; T. xanthochilus is the sister species of T. spinulosus. Tropidurus spinulosus is found to be more closely related to T. strobilurus and a clade of Amazonian species than to T. melanopleurus. The species previously placed in Uracentron are more closely related to species previously placed in Plica than to T. strobilurus as previously thought.

In this collection of papers I have summarized my investigations into the field of evolutionary genetics and more specifically into patterns of biodiversity and evolutionary processes. The lizards (and frogs) studied here share common features in that they are largely present in unique environments, which are also regions that are biologically understudied. Most of these taxa show high degrees of endemism, interesting natural history characteristics, and each group manifests distinctive adaptations of general evolutionary interest. My work in the genus Telmatobius has been a progressive approach that began in my MS program, and it first focused on alpha taxonomy, morphological variation, and species boundaries. This work led to new studies initiated and completed at BYU involving further taxonomic revision (Formas et al., 2003; Chapter 1), and then revisiting and re-evaluating species boundaries established earlier (with allozyme markers) and this time with population level molecular (mitochondrial DNA) markers (Chapter 2). Our results indicate that the striking differences in size, coloration and general appearance in the various Lake Titicaca morphotypes are not genetically based. Further, there is evidence that these morphotypes have evolved very rapidly after demographic bottlenecks eroded present genetic variability. Telmatobius frogs of Lake Titicaca are listed by the International (IUCN) as critically endangered. We support this classification and further suggest studies to explore open questions like the possibility of adaptation along ecological resource gradients. Lizards of the genus Microlophus are interesting but for different reasons, and studies of this group constitutes the bulk of my dissertation work. The genus includes both Galapagos insular species, and continental taxa distributed in a linear gradient along > 4000 km of the western coast of South America. In studying Microlophus I first tackled the unresolved phylogenetic relationships within the genus (Chapter 3) and then pay attention to phylogeographic aspects of the most speciose lizard radiation in the Galapagos Archipelago (Chapter 4). Chapter 3 is a single manuscript provisionally accepted in the journal Systematic Biology. This paper introduces the lizard genus Microlophus (“lava lizards”) as a study system, and includes a large nuclear data set accompanied by an equally large mitochondrial data set (7877 characters in total). This paper explicitly differentiates among sequence alignments of gene regions that vary in tempo and class of mutational events. We show that this recognition is important and we suggest ways to appropriately deal with the alignment of multi-locus non-coding DNA data sets. A secondary finding in this study is that mtDNA and nDNA topologies are discordant with each other but that both are strongly supported, and that the nuclear topology is concordant with species distribution patterns along coastal South America. We hypothesize that in this particular region of the tree, the nuclear genome recovers a topology that is closer to the species tree, and conflicts occur due to likely secondary contact of distantly related taxa, suggesting that unique taxonomic relationships in the mtDNA gene tree are the result of hybridization. This last point highlights the value of dense taxonomic and character sampling for teasing apart different aspects of evolutionary processes. Chapter 4 is a manuscript to be submitted to the journal Evolution; in this study we further investigate the most speciose radiation of Microlophus in the Galapagos, based on an unparalleled sampling of most islands and small islets in the Archipelago. We use mtDNA sequences to both test hypothesized between-island colonization routes, as well as the expectation that within-island phylogeographic structure should be greater on older islands. Our mtDNA gene tree is strongly supported and allows rejection of previous alternatives, and we propose a novel sequence of between-island colonization events. Our results also reject the idea of phylogeographic structure been related solely to island age. Instead, we provide evidence to suggest that active volcanism as a major player in the generation of genetic diversity in within-island environments, and this is further compounded by the seemingly stochastic nature of within-island long-distance colonization routes mediated by ocean currents. We suggest that the direction and intensity of these currents, as currently understood, are insufficient to generate a priori hypotheses of oceanic colonization routes and their influence on gene flow. We do show that the standard stepping-stone model of migration, where genetic interchange is only possible among neighboring localities, does not explain much of the within-island population genetic structure unraveled by this study. From a biological conservation perspective the study of patterns of recent evolutionary history in the Galapagos provides with a window to evolutionary processes that have shaped and continue to impact the generation of biodiversity in the Galapagos Archipelago. Islands have long been viewed as natural laboratories of evolutionary change, and thus all island isolates are or could be distinctly important components of the larger, archipelago-wide processes. We provide working hypotheses for some of the demographic processes that might be generating within- and between-island biodiversity in this clade of lizards; confirmation of these explanations with independent data will have management implications for conserving the unique patterns observed in the Galapagos biota, but also the processes that generated these patterns.