No abstract

Male-biased sexual dimorphism in head, limbs, and tail scaled to snout-vent length has been reported in many lizard species. Consequently, various hypotheses have been proposed to explain observed body-shape dimorphism. According to the majority of them, the proportions of body components are adaptively related to sexual differences in ecology as well as in reproductive behaviour. Our study shows an alternative, much more parsimonious explanation in the common lizard (Lacerta vivipara). According to our analyses, the exaggeration of a single trait, specifically trunk length in females, may explain the whole pattern of sexual differences in body shape. The only consistent adaptive hypothesis, then, is that females with a larger abdominal cavity, and consequently a longer trunk, have a reproductive advantage. Size-adjusted heads, limbs, and tails traditionally reported to be larger in males than in females, features ascribed to numerous evolutionary mechanisms, thus appear to be just an artifact of inappropriate scaling to a sexually dimorphic trait (snout-vent length). As scaling to a single trait has been routinely used in many studies carried out in animals, we warn against quick interpretations based on such analyses and recommend more cautious inspection of allometries.Résumé : On signale un dimorphisme sexuel des tailles de la tête, des membres et de la queue corrigées par rapport à la longueur museau-évent chez plusieurs espèces de lézards, dimorphisme qui favorise les mâles. Diverses hypothèses ont été avancées pour expliquer ce dimorphisme de la forme du corps. La plupart d'entre elles concluent que les proportions des segments du corps sont adaptées aux différences sexuelles d'écologie et de comportement reproducteur. Notre étude met de l'avant une explication de rechange, beaucoup plus parcimonieuse, chez le lézard vivipare (Lacerta vivipara). Selon nos analyses, l'exagération d'un seul caractère, spécifiquement la longueur du tronc chez les femelles, peut expliquer l'ensemble des différences sexuelles de la forme du corps. La seule hypothèse adaptative conséquente est alors que les femelles qui ont une plus grande cavité abdominale, et donc un tronc plus allongé, possèdent un avantage reproductif. Les tailles corrigées de la tête, des membres et de la queue, qui sont alors décrites comme plus grandes chez les mâles que chez les femelles et rattachées à divers mécanismes évolutifs, semblent alors n'être que des artéfacts causés par une correction impropre par rapport à la longueur museau-évent, un caractère à dimorphisme sexuel. Comme la correction par rapport à un seul caractère est couramment utilisée dans plusieurs études sur les animaux, nous mettons en garde contre l'interprétation hâtive des résultats et nous recommandons un examen plus attentif des allométries. [Traduit par la Rédaction] 1117Kratochvíl et al.

Despite their long history with the basal split dating back to the Eocene, all species of monitor lizards (family Varanidae) studied so far share the same chromosome number of 2n = 40. However, there are differences in the morphology of the macrochromosome pairs 5-8. Further, sex determination, which revealed ZZ/ZW sex microchromosomes, was studied only in a few varanid species and only with techniques that did not test their homology. The aim of this study was to (i) test if cryptic interchromosomal rearrangements of larger chromosomal blocks occurred during the karyotype evolution of this group, (ii) contribute to the reconstruction of the varanid ancestral karyotype, and (iii) test homology of sex chromosomes among varanids. We investigated these issues by hybridizing flow sorted chromosome paints from Varanus komodoensis to metaphases of nine species of monitor lizards. The results show that differences in the morphology of the chromosome pairs 5-8 can be attributed to intrachromosomal rearrangements, which led to transitions between acrocentric and metacentric chromosomes in both directions. We also documented the first case of spontaneous triploidy among varanids in Varanus albigularis. The triploid individual was fully grown, which demonstrates that polyploidization is compatible with life in this lineage. We found that the W chromosome differs between species in size and heterochromatin content. The varanid Z chromosome is clearly conserved in all the analyzed species. Varanids, in addition to iguanas, caenophidian snakes, and lacertid lizards, are another squamate group with highly conserved sex chromosomes over a long evolutionary time.

Monitor lizards are unique among ectothermic reptiles in that they have high aerobic capacity and distinctive cardiovascular physiology resembling that of endothermic mammals. Here, we sequence the genome of the Komodo dragon Varanus komodoensis, the largest extant monitor lizard, and generate a high-resolution de novo chromosome-assigned genome assembly for V. komodoensis using a hybrid approach of long-range sequencing and single-molecule optical mapping. Comparing the genome of V. komodoensis with those of related species, we find evidence of positive selection in pathways related to energy metabolism, cardiovascular homoeostasis, and haemostasis. We also show species-specific expansions of a chemoreceptor gene family related to pheromone and kairomone sensing in V. komodoensis and other lizard lineages. Together, these evolutionary signatures of adaptation reveal the genetic underpinnings of the unique Komodo dragon sensory and cardiovascular systems, and suggest that selective pressure altered haemostasis genes to help Komodo dragons evade the anticoagulant effects of their own saliva. The Komodo dragon genome is an important resource for understanding the biology of monitor lizards and reptiles worldwide.

Most lizards feed on a variety of food items that may differ dramatically in their physical and behavioral characteristics. Several lizard families are known to feed upon hard-shelled prey (durophagy). Yet, specializations toward true molluscivory have been documented for only a few species. As snails are hard and brittle food items, it has been suggested that a specialized cranial morphology, high bite forces, and an adapted feeding strategy are important for such lizards. Here we compare head and skull morphology, bite forces, and feeding kinematics of a snail-crushing teiid lizard (Dracaena guianensis) with those in a closely related omnivorous species (Tupinambis merianae). Our data show that juvenile D. guianensis differ from T. merianae in having bigger heads and greater bite forces. Adults, however, do not differ in bite force. A comparison of feeding kinematics in adult Dracaena and Tupinambis revealed that Dracaena typically use more transport cycles, yet are more agile in manipulating snails. During transport, the tongue plays an important role in manipulating and expelling shell fragments before swallowing. Although Dracaena is slow, these animals are very effective in crushing and processing hard-shelled prey.

We developed new tools to build a high-quality chromosomal map of the Komodo dragon (Varanus komodoensis) available for cross-species phylogenomic analyses. First, we isolated chromosomes by flow sorting and determined the chromosome content of each flow karyotype peak by FISH. We then isolated additional Komodo dragon chromosomes by microdissection and amplified chromosome-specific DNA pools. The chromosome-specific DNA pools can be sequenced, assembled, and mapped by next-generation sequencing technology. The chromosome-specific paint probes can be used to investigate karyotype evolution through cross-species chromosome painting. Overall, the set of chromosome-specific DNA pools of V. komodoensis provides new tools for detailed phylogenomic analyses of Varanidae and squamates in general.

No abstract

The Komodo dragon (Varanus komodoensis) is the largest lizard in the world. Surprisingly, it has not yet been cytogenetically examined. Here, we present the very first description of its karyotype and sex chromosomes. The karyotype consists of 2n = 40 chromosomes, 16 macrochromosomes and 24 microchromosomes. Although the chromosome number is constant for all species of monitor lizards (family Varanidae) with the currently reported karyotype, variability in the morphology of the macrochromosomes has been previously documented within the group. We uncovered highly differentiated ZZ/ZW sex microchromosomes with a heterochromatic W chromosome in the Komodo dragon. Sex chromosomes have so far only been described in a few species of varanids including V. varius, the sister species to Komodo dragon, whose W chromosome is notably larger than that of the Komodo dragon. Accumulations of several microsatellite sequences in the W chromosome have recently been detected in 3 species of monitor lizards; however, these accumulations are absent from the W chromosome of the Komodo dragon. In conclusion, although varanids are rather conservative in karyotypes, their W chromosomes exhibit substantial variability at the sequence level, adding further evidence that degenerated sex chromosomes may represent the most dynamic genome part.