Le sommeil constitue un comportement vital complexe, identifié chez la quasi-totalité des animaux étudiés. Sur la base d’études princeps dans les années 50 chez le chat et l’homme, le sommeil a pu être séparé clairement en deux états distincts : le sommeil lent et le sommeil paradoxal. Ces deux états ont ainsi été caractérisés sur la base de critères électroencéphalographiques, physiologiques et comportementaux. Basé sur une définition mammalienne, il a ainsi été montré que les mammifères terrestres et les oiseaux, tous deux homéothermes, possédaient ces deux états de sommeil. Cependant, l'origine évolutive de ces deux états reste inconnue et nous ne savons toujours pas s’ils ont évolué de façon indépendante ou s’ils ont été hérités d'un ancêtre commun. Les amphibiens et les reptiles, positionnés à la base des tétrapodes et des amniotes constituent par conséquent, des taxons clés dans la compréhension de l'évolution de ces deux états de sommeil. Afin de mieux comprendre la phylogénie de ces deux états, nous avons réalisé dans un premier temps une revue et méta-analyse de la littérature du sommeil chez ces espèces. Dans un second temps, et dans le but de pouvoir conduire des approches comparatives et ainsi mieux décrire la plasticité du sommeil, nous avons développé un dispositif miniature sans fil permettant d’enregistrer simultanément l’électrophysiologie, la physiologie, la température et le comportement en laboratoire et en milieu naturel. Enfin, nous avons conduit une étude électrophysiologique, physiologique, pharmacologique et comportementale chez deux espèces de squamates (Salvator merianae et Pogona vitticeps). Cette étude nous a permis de montrer que deux états électroencéphalographiques de sommeil existaient chez ces espèces. Cependant, elles ont aussi révélé des divergences phénotypiques importantes au sein même des lézards, ainsi qu’avec le sommeil des mammifères et des oiseaux, démontrant ainsi une origine commune mais complexe des deux états de sommeil / Sleep is a vital and complex behavior, identified in nearly all animals. Based on studies on cats and humans conducted in the 50’s, sleep was separated into two distinct sleep states: slow wave sleep and paradoxical sleep (or REM sleep). Those two states were identified based on electroencephalographic, physiological and behavioral parameters. Based on this mammalian definition, it has been demonstrated that those two states exist in terrestrial mammals and birds, both homeotherms. However, the evolutive origin of these sleeps states remains unknown and we do not know whether they evolved independently or if they were inherited from a common ancestor. Amphibians and reptiles are respectively positioned at the base of the tetrapod and the amniote tree. Therefore, they constitute key taxa in the understanding of the origin of these states. In order to understand the phylogeny of these states, we first performed an exhaustive review and meta-analysis of the sleep literature in these groups. Next, in order to be able to conduct comparative approaches and better understand the sleep plasticity, we developed a standalone miniature device to record electrophysiology, physiology, temperature, and behavior simultaneously and this under both lab and field conditions. Finally, we conducted an electrophysiological, physiological, pharmacological and behavioral study of two squamates species (Salvator merianae and Pogona vitticeps). This study revealed that two electro-encephalographical sleep states exist in these species. However, they also showed that the phenotype of these states diverged between the two lizards and between the lizards on the one hand and mammals and birds on the other hand. This would suggest a common, but complex, origin of these two sleep states

Fossil Agamidae from Western Australia have been the subject of limited study. To aid in fossil agamid identification, Hocknull (2002) examined the maxilla and dentary of several extant species from Australia and determined diagnostic characters for various species groups. In the study here, fossil agamids from two localities in Western Australia, Hastings Cave and Horseshoe Cave, were examined, grouped, and identified to the lowest unambiguous taxonomic level. Morphometric analyses were conducted to compare morphotypes, and find additional diagnostic characters. From Hastings Cave there were two maxilla morphotypes and three dentary morphotypes. Based on identifications, taxa present at this locality were Pogona and Ctenophorus. Horseshoe Cave contained three maxilla morphotypes and two dentary morphotypes; taxa present were Pogona, Tympanocryptis, and Ctenophorus. Morphometric analyses showed separation between groups; however, the dentary morphotype separation was not as clear. Each morphotype identification matched a species in the respective localities today, but identifications are cautious.

Background: As the climate warms, many species of reptiles are at risk of habitat loss and ultimately extinction. Locations of suitable habitat in the past, present, and future were modeled for several lizard species using MaxEnt, incorporating climatic variables related to temperature and precipitation. In this study, we predict where there is currently suitable habitat for the genus Pogona and potential shifts in habitat suitability in the past and future. Methods: Georeferenced occurrence records were obtained from the Global Biodiversity Information Facility, climate variables (describing temperature and precipitation) were obtained from WorldClim, and a vegetation index was obtained from AVHRR satellite data. Matching climate variables were downloaded for three different past time periods (mid-Holocene, Last Glacial Maximum, and Last Interglacial) and two different future projections representative concentration pathways (RCPs 2.6 and 8.5). MaxEnt produced accuracy metrics, response curves, and probability surfaces. For each species, parameters were adjusted for the best possible output that was biologically informative. Results: Model results predicted that in the past, there was little suitable habitat for P. henrylawsoni and P. microlepidota within the areas of their current range. Past areas of suitable habitat for P. barbata were predicted to be similar to the current prediction. Pogona minor and P. nullarbor were predicted to have had a more expansive range of suitable habitat in the past, which has reduced over time. P. vitticeps was predicted to have less suitable habitat in the past when examining the region of their known occurrence; however, there was predicted growth in suitable habitat in Western Australia. Both 2070 models predict a similar distribution of habitat; however, the model produced using the 2070 RCP 8.5 climate change projection showed a larger change, both in areas of suitable habitat gain and loss. In the future, P. henrylawsoni and P. microlepidota might gain suitable habitat, while the other four species could possibly suffer habitat loss. Discussion: Based on the model results, P. henrylawsoni and P. microlepidota had minimal areas of suitable habitat during the Last Glacial Maximum, possibly due to changes in tolerance or data/model limitations, especially since genetic analyses for these species suggest a much earlier emergence. The predicted late Quaternary habitat results for all species of Pogona are conservative and should be compared to the fossil record which is not possible at the moment due to the current inability to identify fossil Pogona to the species level. P. nullarbor and P. vitticeps future models predict substantial habitat loss. P. nullarbor could potentially be considered vulnerable in the present since it already has a restricted range, and a conservation plan may need to be considered.

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Sex determination among reptiles is a very variable matter across it's taxa. We meet there temperature sex determination and genotypic sex determination with many independent transitions between them. It is a group suitable to study evolution of sex determination, sex chromosomes and sex determination genes. Rare cases of sex reversal caused by extreme incubation temperature or exogenous hormones have been reported in recent years. In case of Acrodont lizard, Pogona vitticeps, was reported sex reversal caused by high incubation temperatures. Our purpose was to repeat the experiment, mainly due to insufficient conclusiveness of used methods. We wanted to expand the experiment by hormonal reversal, studying persistence of sex reversal to maturity and fertility of reversed individuals. We managed successfully to demonstrate sex reversal in both treatments by histological examination. Individuals with discordant phenotypic and genotypic sex were breed till one year of life, which demonstrate persistence of reversal. Our outcomes are concordant with most recent work on this species and show full functional phenomenon of sex reversal with reptiles, which studying could contribute to our understanding of evolution of sex determination.