Abstract:The egg tooth is a hatching adaptation, characteristic of all squamates. In brown anole embryos, the first tooth that starts differentiating is the egg tooth. It develops from a single tooth germ and, similar to the regular dentition of all the other vertebrates, the differentiating egg tooth of the brown anole passes through classic morphological and developmental stages named according to the shape of the dental epithelium: epithelial thickening, dental lamina, tooth bud, cap and bell stages. The differentia… Show more
“…2019; Hermyt et al . 2020), but this can arise in different ways. In snakes, a single egg tooth can arise from the fusion of paired adjacent tooth germs during early embryonic stages (Fons et al .…”
Section: Discussionmentioning
confidence: 99%
“…2019), but in lizards, a median egg tooth can result from the degeneration of one of an original pair of egg teeth or from a single median tooth germ (De Beer, 1949; Hermyt et al . 2020). The egg tooth or teeth are lost a few days post hatching, and replaced by adult premaxillary teeth (Trauth, 1988).…”
Tarentola annularis is a climbing gecko with a wide distribution in Africa north of the equator. In the present paper, we describe the development of the osteocranium of this lizard, from the first appearance of the cranial elements up to the point of hatching. This is based on a combination of histology and cleared and stained specimens. This is the first comprehensive account of gekkotan pre‐hatching skull development based on a comprehensive series of embryos, rather than a few selected stages. Given that Gekkota is now widely regarded as representing the sister group to other squamates, this account helps to fill a significant gap in the literature. Moreover, as many authors have considered features of the gekkotan skull and skeleton to be indicative of paedomorphosis, it is important to know whether this hypothesis is supported by delays in the onset of cranial ossification. In fact, we found the sequence of cranial bone ossification to be broadly comparable to that of other squamates studied to date, with no significant lags in development.
“…2019; Hermyt et al . 2020), but this can arise in different ways. In snakes, a single egg tooth can arise from the fusion of paired adjacent tooth germs during early embryonic stages (Fons et al .…”
Section: Discussionmentioning
confidence: 99%
“…2019), but in lizards, a median egg tooth can result from the degeneration of one of an original pair of egg teeth or from a single median tooth germ (De Beer, 1949; Hermyt et al . 2020). The egg tooth or teeth are lost a few days post hatching, and replaced by adult premaxillary teeth (Trauth, 1988).…”
Tarentola annularis is a climbing gecko with a wide distribution in Africa north of the equator. In the present paper, we describe the development of the osteocranium of this lizard, from the first appearance of the cranial elements up to the point of hatching. This is based on a combination of histology and cleared and stained specimens. This is the first comprehensive account of gekkotan pre‐hatching skull development based on a comprehensive series of embryos, rather than a few selected stages. Given that Gekkota is now widely regarded as representing the sister group to other squamates, this account helps to fill a significant gap in the literature. Moreover, as many authors have considered features of the gekkotan skull and skeleton to be indicative of paedomorphosis, it is important to know whether this hypothesis is supported by delays in the onset of cranial ossification. In fact, we found the sequence of cranial bone ossification to be broadly comparable to that of other squamates studied to date, with no significant lags in development.
“…It is known that all the egg teeth in unidentates are located in the midline of the frontal part of the palate (Fons et al, 2019;Hermyt et al, 2020Hermyt et al, , 2017Smith et al, 1953). They have varying spatial orientation, which in some cases can change in the course of embryonic development.…”
Section: Localization and Spatial Orientationmentioning
confidence: 99%
“…However, these fibers and long axes of cells located among them are oriented in the leftright axis. In previously investigated unidentates they are oriented in the dorsoventral axis (Hermyt et al, 2020(Hermyt et al, , 2017. It is possible that differences, both in terms of attachment and fiber orientation, result from different positions of gekkotan egg teeth, and different premaxilla shape.…”
Section: Attachment and Implantationmentioning
confidence: 99%
“…Leopard gecko egg teeth have similar shape and curvature as previously described egg teeth of unidentates. They differ from them in terms of spatial orientation, attachment tissue, and localization on the premaxilla (Fons et al, 2019;Hermyt et al, 2020Hermyt et al, , 2017Smith et al, 1953). Egg teeth of mourning geckos are distinct from other teeth and even from egg teeth of other squamate species in having a vessel; D, dentin; DL, dental lamina; DP, dental pulp; EO, enamel organ; ET, egg tooth; NC, nasal capsule; OB, odontoblasts; PMX, premaxilla; SR, stellate reticulum caudoventrally oriented cusps at their tip which might be connected with different hardness of their eggshell.…”
Section: Different Ways Of Hatching In Geckosmentioning
The egg tooth of squamates evolved to facilitate hatching from mineralized eggshells. Squamate reptiles can assist their hatching with a single unpaired egg tooth (unidentates) or double egg teeth (geckos and dibamids). Egg tooth ontogeny in two gekkotan species, the leopard gecko Eublepharis macularius and the mourning gecko Lepidodactylus lugubris, was compared using microtomography, scanning electron microscopy, and light microscopy. Investigated species are characterized by different hardnesses of their eggshells. Leopard geckos eggs have a relatively soft and flexible parchment (leathery) shell, while eggshells of mourning geckos are hard and rigid. Embryos of both species, like other Gekkota, have double egg teeth, but the morphology of these structures differs between the investigated species. These differences in shape, localization, and spatial orientation were present from the earliest stages of embryonic development. In mourning gecko, anlagen of differentiating egg teeth change their position on the palate during embryonic development. Initially they are separated by condensed mesenchyme, but later in development, their enamel organs are connected. In leopard geckos, the localization of egg tooth germs does not change, but their spatial orientation does. Egg teeth of this species shift from inward to outward orientation. This is likely related to differences in structure and mechanical properties of eggshells in the studied species. In investigated species, two hatching mechanisms are possible during emergence of young individuals. We speculate that mourning geckos break the eggshell through puncturing action with egg teeth, similar to the pipping phase of chick and turtles embryos. Egg teeth of leopard geckos cut egg membranes similarly to most squamates. Our results also revealed differences in egg tooth implantation between Gekkota and Unidentata: gekkotan egg teeth are subthecodont (in shallow sockets), while those in unidentates are acrodont (attached to the top of the alveolar ridge).
The sensory olfactory epithelium and the vomeronasal sensory epithelium (VSE) are characterized by continuous turnover of the receptor cells during postnatal life and are capable of regeneration after injury. The VSE, like the entire vomeronasal organ, is generally well developed in squamates and is crucial for detection of pheromones and prey odors. Despite the numerous studies on embryonic development of the VSE in squamates, especially in snakes, an ultrastructural analysis, as far as we know, has never been performed. Therefore, we investigated the embryology of the VSE of the grass snake (Natrix natrix) using electron microscopy (SEM and TEM) and light microscopy. As was shown for adult snakes, the hypertrophied ophidian VSE may provide great resolution of changes in neuron morphology located at various epithelial levels. The results of this study suggest that different populations of stem/progenitor cells occur at the base of the ophidian VSE during embryonic development. One of them may be radial glia‐like cells, described previously in mouse. The various structure and ultrastructure of neurons located at different parts of the VSE provide evidence for neuronal maturation and aging. Based on these results, a few nonmutually exclusive hypotheses explaining the formation of the peculiar columnar organization of the VSE in snakes were proposed.
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