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Os viperídeos estão entre as serpentes de menor custo energético de manutenção, o que é, geralmente, relacionado a seus baixos níveis de deslocamento e a tática de forrageio por emboscada. Dois importantes componentes do alocamento energético destes animais são: 1) o metabolismo de repouso padrão, que está relacionado ao custo de manutenção visceral durante o repouso e 2) o aumento metabólico pós-prandial (AMPP), que está relacionado ao custo do processo digestório. O presente trabalho teve como objetivos estudar as variações da TMRP (taxa metabólica de repouso padrão) e do AMPP em 5 espécies pertencentes ao gênero Bothrops levando em conta aspectos filogenéticos, ontogenéticos e testando hipóteses acerca de possíveis variações destes componentes em função de características ecológicas. Além disso, o presente trabalho testou, através de ferramentas de ponderação filogenética, a hipótese atualmente aceita que prediz que as TMRPs em serpentes estão essencialmente ligadas a estratégia alimentar e não a filogenia. O trabalho está dividido em quatro capítulos, sendo o primeiro devotado a uma introdução geral acerca dos assuntos que serão abordados nos demais. Os resultados e discussões específicas estão divididos em dois capítulos redigidos em forma de artigo, primeiro referente aos estudos das taxas metabólicas de repouso (capítulo 2) e o segundo sobre o AMPP (capítulo 3). Por fim, a conclusão final acerca dos achados e as perspectivas para pesquisas futuras estão presente no capítulo 4. / The viperids are among the snakes with the lowest energetic maintenance costs which are generally related to the low mobility and ambush foraging mode. Two important components of energy allocation in these animals are 1) standard metabolic rates (SMR), related to the cost of keeping visceral components during resting and 2) specific dynamic action (SDA) , which is related to the cost of digestion. The present work aimed to study the variations of SMR and SDA in 5 species of the genus Bothrops taking into account aspects of phylogeny and ontogeny plus testing hypotheses about possible variations in these metabolic rates related to ecological characteristics. Furthermore, the present study used phylogenetic weighting tools to test the currently accepted hypothesis that predicts that SMR in snakes is related to the feeding strategy and not to phylogeny. The work is divided into four different chapters. Chapter 1 is devoted to a general introduction about the issues that will be addressed in the others chapters. The results and discussions are divided into two chapters presented as articles, the first referring to studies of SMR ( chapter 2 ) and the second to the SDA (chapter 3 ). Finally, in chapter 4 we include the final conclusion and prospects for future research

The pepsinogens and pepsins of cobra, mole snake and puff adder have been studied. The pepsinogens of all three species fall into two distinct groups, here designated PI and PII. At least the latter group, in all cases, shows substantial microheterogeneity. Physicochemical studies suggest that the cobra and puff adder PII groups are more similar to each other than either is to the mole snake PII group. Kinetic studies indicate that, in the cobra and mole snake, the PI and PII pepsins differ in their Arrhenius activation energies. Such difference is smaller, or absent, in the case of the puff adder PI and PII pepsins. These characteristics of the pepsins are assessed in the context of the differences between the oral secretions of the three species studied. The suggestion is advanced that the puff adder's strongly proteolytic venom has influenced certain properties of its gastric proteases.

The reptilian clade Squamata is defined primarily by osteological synapomorphies, few of which are entirely unambiguous. Studies of developing squamate eggs have revealed a uniquely specialized feature not known to occur in any other amniotes. This feature—the yolk cleft/isolated yolk mass complex—lines the ventral hemisphere of the egg. During its formation, extraembryonic mesoderm penetrates the yolk and an exocoelom (the yolk cleft [YC]) forms in association with it, cutting off a thin segment of yolk (the “isolated yolk mass” [IYM]) from the main body of the yolk. The YC–IYM complex has been observed and described in more than 65 squamate species in 12 families. In viviparous species, it contributes to the “omphaloplacenta,” a type of yolk sac placenta unique to squamates. The only squamates known to lack the IYM are a few highly placentotrophic skinks with minuscule eggs, viviparous species in which it clearly has been lost. Given its absence in mammals, chelonians, crocodylians, and birds, the YC–IYM complex warrants recognition as a developmental synapomorphy of the squamate clade. As in extant viviparous lizards and snakes, the YC–IYM complex presumably contributed to the placenta of extinct viviparous squamates.

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Gap crossing is a regular locomotor activity for arboreal animals. The distance between branches likely plays a role in determining whether an animal is capable of crossing a given gap, and what locomotor behavior it uses to do so. Yet, despite the importance of gap distance as a physical parameter influencing gap crossing behavior, the precise relationships between gap distance and movement kinematics have been explored in only a very small number of species. One particularly interesting group of arboreal inhabitants are the flying snakes (Chrysopelea). This species is able to use a dynamic "J-loop" movement to launch its glides, but it is not known whether it is also capable of using such jumps to cross smaller gaps between tree branches. This dissertation addresses this knowledge gap, and investigates the influence of gap distance on crossing behavior and kinematics in three closely-related species of snake: Chrysopelea paradisi, a species of flying snake, and two species from the sister genus, Dendrelaphis, neither of which can glide. Chapter 2 is a literature review of the biomechanics of gap crossing, specifically focusing on the role played by gap distance, and establishes the context for the rest of the work. Chapter 3 presents a detailed study of how increasing gap size influences the behavior and kinematics of gap crossing in C. paradisi, showing that this species uses increasingly dynamic movements to cross gaps of increasing size. Chapter 4 explores the same relationships between gap size and kinematics in D. punctulatus and D. calligastra, revealing remarkable similarities between the three species, suggesting the possibility that dynamic gap crossing may have evolved prior to gliding in this clade. Finally, chapter 5 addresses the role played by gap distance in limiting the non-dynamic, cantilever movements used by these species to cross small gaps, comparing observed stopping distances to those predicted by various torque-related limitations. / Doctor of Philosophy / To successfully cross a gap, an animal must be able to reach or jump from one side to the other. Animals who live in trees must do this quite frequently, as they live among the branches and there are often not connected paths from one place to another. But we don't know very much about how the distance between two structures (the "gap distance") affects the ways an animal moves between them. In this dissertation, I explore how gap distance changes the way a few special species of snakes cross a gap. The species I am studying are special because one species, the paradise tree snake, can glide. Because this 'flying' snake launches its glides by doing a big jump, it is possible that the snake can also jump between tree branches, but this question has never been examined before. We also don't know how the ability to do big jumps evolved, so I studied how distance affects the way two very closely related species of snake, the common tree snake and the northern tree snake, cross gaps. By looking at all of these species, we can understand more about what kinds of behavior are specific to the flying snakes, and which are present in related species. Finally, I also explore how gap distance limits the way the snakes cross gaps when they are not jumping. When the snakes do not jump, they have to hold themselves out straight off the end of a branch. This requires a lot of muscular effort, which means they can't go as far. The fact that the non-jumping behavior is distance-limited might help explain why the snakes need to jump. Altogether, the projects in this study help us understand how gap distance influences what behavior an animal chooses to cross the gap, and increases our knowledge of how flying snakes and their relatives cross gaps in particular.