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Lepidosauria

The Lepidosauria (/ˌlɛpɪdˈsɔːriə/, from Greek meaning scaled lizards) is a subclass or superorder of reptiles, containing the orders Squamata and Rhynchocephalia. Squamata includes lizards and snakes.[2] Squamata contains over 9,000 species, making it by far the most species-rich and diverse order of non-avian reptiles in the present day.[3] Rhynchocephalia was a formerly widespread and diverse group of reptiles in the Mesozoic Era.[4] However, it is represented by only one living species: the tuatara (Sphenodon punctatus), a superficially lizard-like reptile native to New Zealand.[5][6]

Lepidosaurs
Temporal range:
Middle Triassic - Present,[1] 240–0 Ma
Collage of five lepidosaurs. Clockwise from top left: tuatara, black mamba, green iguana, Smaug breyeri and reticulated python
Scientific classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Clade: Lepidosauromorpha
Superorder: Lepidosauria
Haeckel, 1866
Orders

Lepidosauria is a monophyletic group (i.e. a clade), containing all descendants of the last common ancestor of squamates and rhynchocephalians.[7] Lepidosaurs can be distinguished from other reptiles via several traits, such as large keratinous scales which may overlap one another. Purely in the context of modern taxa, Lepidosauria can be considered the sister taxon to Archosauria, which includes Aves (birds) and Crocodilia. Testudines (turtles) may be related to lepidosaurs or to archosaurs, but no consensus has been reached on this subject. Lepidosauria is encompassed by Lepidosauromorpha, a broader group defined as all reptiles (living or extinct) closer to lepidosaurs than to archosaurs.

Evolution edit

Lepidosauromorpha is thought to have split off from the ancestor of Archelosauria during the Permian period.[8] The earliest members of Lepidosauromorpha date the Early Triassic. Sophineta from the Early Triassic may be the oldest known lepidosaur, but its exact placement is uncertain.[9] The earliest rhynchocephalian, Wirtembergia, is known from the Middle Triassic.[10] While the lepidosaur Megachirella may represent a stem-group squamate from the Middle Triassic[11] the earliest modern members of the group are known from the Middle Jurassic.[12] Squamates underwent a great radiation in the Cretaceous,[13] while rhynchocephalians declined during the same time period.[14]

Description edit

Extant reptiles are in the clade Diapsida, named for two pairs temporal fenestrae present on the skull behind the eye socket.[15] Until recently, Diapsida was said to be composed of Lepidosauria and their sister taxa Archosauria.[16] The subclass Lepidosauria is then split into Squamata[17] and Rhynchocephalia. More recent morphological studies[18][19] and molecular studies[20][21][22][23][24][25] also place turtles firmly within Diapsida, even though they lack temporal fenestrations.

 
The quadrate bone is particularly elongated in snakes, to facilitate cranial kinesis

The reptiles in the subclass Lepidosauria can be distinguished from other reptiles by a variety of characteristics.[26] Lepidosaurs are suggested to be distinguished from more primitive lepidosauromorphs by the development of a conch on the quadrate, allowing for the development of a tympanic membrane in the ear (a trait lost in the tuatara, but present in early rhynchocephalians), as well as the development of a subolfactory process on the frontal bones of the skull.[9][27]

 
Schematic skull of a squamate showing the location of major dermal bones

The group Squamata[17] includes snakes, lizards, and amphisbaenians. Squamata can be characterized by the reduction or loss of limbs. Snakes and legless lizards have evolved the complete loss of their limbs. The upper jaw of Squamates is movable on the cranium, a configuration called kinesis.[28] This is made possible by a loose connection between the quadrate and its neighboring bones.[29] Without this, snakes would not be able consume prey that are much larger than themselves. Amphisbaenians are mostly legless like snakes, but are generally much smaller. Three species of amphisbaenians have kept reduced front limbs and these species are known for actively burrowing in the ground.[30] The tuatara and some extinct rhynchocephalians have a more rigid skull with a complete lower temporal bar closing the lower temporal fenestra formed by the fusion of the jugal and quadrate/quadratojugal bones, similar to the condition found in primitive diapsids. However early rhynchocephalians and lepidosauromorphs had an open lower temporal fenestra, without a complete temporal bar, so this is thought to be a reversion rather than retention. The temporal bar is thought to stabilise the skull during biting.[31]

Male squamates have evolved a pair of hemipenises instead of a single penis with erectile tissue that is found in crocodilians, birds, mammals, and turtles. The hemipenis can be found in the base of the tail. The tuatara does not have a hemipenis, but instead has shallow paired outpocketings of the posterior wall of the cloaca.[16]

 
The foot of a skink, showing lepidosaurs' characteristic overlapping scales

Second, most lepidosaurs have the ability to autotomize their tails. However, this trait has been lost on some recent species. In lizards and rhynchoc, fracture planes are present within the vertebrae of the tail that allow for its removal. Some lizards have multiple fracture planes, while others just have a single fracture plane. The regrowth of the tail is not always complete and is made of a solid rod of cartilage rather than individual vertebrae.[16] In snakes, the tail separates between vertebrae and some do not experience regrowth.[16]

Third, the scales in lepidosaurs are horny (keratinized) structures of the epidermis, allowing them to be shed collectively, contrary to the scutes seen in other reptiles.[16] This is done in different cycles, depending on the species. However, lizards generally shed in flakes while snakes shed in one piece. Unlike scutes, lepidosaur scales will often overlap like roof tiles.

Biology and ecology edit

 
Python (top) and rattlesnake (bottom) featuring pit organs for infrared sensing. Red arrows indicating pit organs and black arrows pointing to the nostrils

Squamates are represented by viviparous, ovoviviparous, and oviparous species. Viviparous means that the female gives birth to live young, Ovoviviparous means that the egg will develop inside the female's body and Oviparous means that the female lays eggs. A few species within Squamata have the ability to reproduce asexually.[32] The tuatara lays eggs that are usually about one inch in length and which take about 14 months to incubate.[28]

While in the egg, the Squamata embryo develops an egg tooth on the premaxillary that helps the animal emerge from the egg.[33] A reptile will increase three to twentyfold in length from hatching to adulthood.[33] There are three main life history events that lepidosaurs reach: hatching/birth, sexual maturity, and reproductive senility.[33]

Because gular pumping is so common in squamates, and is also found in the tuatara, it is assumed that it is an original trait in the group.[34]

Most lepidosaurs rely on camouflage as one of their main defenses. Some species have evolved to blend in with their ecosystem, while others are able to change their skin color to blend in with their current surroundings. The ability to autotomize the tail is another defense that is common among lepidosaurs. Other species, such as the Echinosauria, have evolved the defense of feigning death.[33]

Hunting and diet edit

 
A green crested lizard feeding on an invertebrate

Viperines can sense their prey's infrared radiation through bare nerve endings on the skin of their heads.[33] Also, viperines and some boids have thermal receptors that allow them to target their prey's heat.[33] Many snakes are able to obtain their prey through constriction. This is done by first biting the prey, then coiling their body around the prey. The snake then tightens its grip as the prey struggles, which leads to suffocation.[33] Some snakes have fangs that produce venomous bites, which allows the snake to consume unconscious, or even dead, prey. Also, some venoms include a proteolytic component that aids in digestion.[33] Chameleons grasp their prey with a projectile tongue. This is made possible by a hyoid mechanism, which is the contraction of the hyoid muscle that drives the tip of the tongue outwards.[33]

 
An eastern blue-tongued lizard preyed upon by an eastern brown snake

Within the subclass Lepidosauria there are herbivores, omnivores, insectivores, and carnivores. The herbivores consist of iguanines, some agamids, and some skinks.[33] Most lizard species and some snake species are insectivores. The remaining snake species, tuataras, and amphisbaenians, are carnivores. While some snake species are generalist, others eat a narrow range of prey - for example, Salvadora only eat lizards.[33] The remaining lizards are omnivores and can consume plants or insects. The broad carnivorous diet of the tuatara may be facilitated by its specialised shearing mechanism, which involves a forward movement of the lower jaw following jaw closure.[35]

While birds, including raptors, wading birds and roadrunners, and mammals are known to prey on reptiles, the major predator is other reptiles. Some reptiles eat reptile eggs, for example the diet of the Nile monitor includes crocodile eggs, and small reptiles are preyed upon by larger ones.[33]

Conservation edit

 
Global range of lizard species

The geographic ranges of lepidosaurs are vast and cover all but the most extreme cold parts of the globe. Amphisbaenians exist in Florida, mainland Mexico, including Baja California, the Mediterranean region, the Middle East, North Africa, sub-Saharan Africa, South America, and the Caribbean.[29] The tuatara is confined to only a few rocky islands of New Zealand, where it digs burrows to live in and preys mostly on insects.[28]

Climate change has led to the need for conservation efforts to protect the existence of the tuatara. This is because it is not possible for this species to migrate on its own to cooler areas. Conservationists are beginning to consider the possibility of translocating them to islands with cooler climates.[36] The range of the tuatara has already been minimized by the introduction of cats, rats, dogs, and mustelids to New Zealand.[37] The eradication of the mammals from the islands where the tuatara still survives has helped the species increase its population. An experiment observing the tuatara population after the removal of the Polynesian rat showed that the tuatara expressed an island-specific increase of population after the rats' removal.[38] However, it may be difficult to keep these small mammals from reinhabiting these islands.

Habitat destruction is the leading negative impact of humans on reptiles. Humans continue to develop land that is important habitat for the lepidosaurs. The clear-cutting of land has also led to habitat reduction. Some snakes and lizards migrate toward human dwellings because there is an abundance of rodent and insect prey. However, these reptiles are seen as pests and are often exterminated.[16]

Interactions with humans edit

 
Boots made from snake skin, the three closest from diamondback rattlesnakes

Snakes are commonly feared throughout the world. Bounties were paid for dead cobras under the British Raj in India; similarly, there have been advertised rattlesnake roundups in North America. Data shows that between 1959 and 1986 an average of 5,563 rattlesnakes were killed per year in Sweetwater, Texas, due to rattlesnake roundups, and these roundups have led to documented declines and local extirpations of rattlesnake populations, especially Eastern Diamondbacks in Georgia.[16]

People have introduced species to the lepidosaurs' natural habitats that have increased predation on the reptiles. For example, mongooses were introduced to Jamaica from India to control the rat infestation in sugar cane fields. As a result, the mongooses fed on the lizard population of Jamaica, which has led to the elimination or decrease of many lizard species.[16] Actions can be taken by humans to help endangered reptiles. Some species are unable to be bred in captivity, but others have thrived. There is also the option of animal refuges. This concept is helpful to contain the reptiles and keep them from human dwellings. However, environmental fluctuations and predatorial attacks still occur in refuges.[33]

Reptile skins are still being sold. Accessories, such as shoes, boots, purses, belts, buttons, wallets, and lamp shades, are all made out of reptile skin.[16] In 1986, the World Resource Institute estimated that 10.5 million reptile skins were traded legally. This total does not include the illegal trades of that year.[16] Horned lizards are popularly harvested and stuffed.[16] Some humans are making a conscious effort to preserve the remaining species of reptiles, however.

References edit

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External links edit

lepidosauria, ɔː, from, greek, meaning, scaled, lizards, subclass, superorder, reptiles, containing, orders, squamata, rhynchocephalia, squamata, includes, lizards, snakes, squamata, contains, over, species, making, most, species, rich, diverse, order, avian, . The Lepidosauria ˌ l ɛ p ɪ d oʊ ˈ s ɔː r i e from Greek meaning scaled lizards is a subclass or superorder of reptiles containing the orders Squamata and Rhynchocephalia Squamata includes lizards and snakes 2 Squamata contains over 9 000 species making it by far the most species rich and diverse order of non avian reptiles in the present day 3 Rhynchocephalia was a formerly widespread and diverse group of reptiles in the Mesozoic Era 4 However it is represented by only one living species the tuatara Sphenodon punctatus a superficially lizard like reptile native to New Zealand 5 6 LepidosaursTemporal range Middle Triassic Present 1 240 0 Ma PreꞒ Ꞓ O S D C P T J K Pg N Collage of five lepidosaurs Clockwise from top left tuatara black mamba green iguana Smaug breyeri and reticulated python Scientific classification Domain Eukaryota Kingdom Animalia Phylum Chordata Class Reptilia Clade Lepidosauromorpha Superorder LepidosauriaHaeckel 1866 Orders Rhynchocephalia Vellbergia Pan Squamata Sophineta Megachirella Marmoretta Tamaulipasaurus Hongshanxi Bellairsia Oculudentavis Huehuecuetzpalli Squamata Lepidosauria is a monophyletic group i e a clade containing all descendants of the last common ancestor of squamates and rhynchocephalians 7 Lepidosaurs can be distinguished from other reptiles via several traits such as large keratinous scales which may overlap one another Purely in the context of modern taxa Lepidosauria can be considered the sister taxon to Archosauria which includes Aves birds and Crocodilia Testudines turtles may be related to lepidosaurs or to archosaurs but no consensus has been reached on this subject Lepidosauria is encompassed by Lepidosauromorpha a broader group defined as all reptiles living or extinct closer to lepidosaurs than to archosaurs Contents 1 Evolution 2 Description 3 Biology and ecology 3 1 Hunting and diet 4 Conservation 4 1 Interactions with humans 5 References 6 External linksEvolution editLepidosauromorpha is thought to have split off from the ancestor of Archelosauria during the Permian period 8 The earliest members of Lepidosauromorpha date the Early Triassic Sophineta from the Early Triassic may be the oldest known lepidosaur but its exact placement is uncertain 9 The earliest rhynchocephalian Wirtembergia is known from the Middle Triassic 10 While the lepidosaur Megachirella may represent a stem group squamate from the Middle Triassic 11 the earliest modern members of the group are known from the Middle Jurassic 12 Squamates underwent a great radiation in the Cretaceous 13 while rhynchocephalians declined during the same time period 14 Description editExtant reptiles are in the clade Diapsida named for two pairs temporal fenestrae present on the skull behind the eye socket 15 Until recently Diapsida was said to be composed of Lepidosauria and their sister taxa Archosauria 16 The subclass Lepidosauria is then split into Squamata 17 and Rhynchocephalia More recent morphological studies 18 19 and molecular studies 20 21 22 23 24 25 also place turtles firmly within Diapsida even though they lack temporal fenestrations nbsp The quadrate bone is particularly elongated in snakes to facilitate cranial kinesisThe reptiles in the subclass Lepidosauria can be distinguished from other reptiles by a variety of characteristics 26 Lepidosaurs are suggested to be distinguished from more primitive lepidosauromorphs by the development of a conch on the quadrate allowing for the development of a tympanic membrane in the ear a trait lost in the tuatara but present in early rhynchocephalians as well as the development of a subolfactory process on the frontal bones of the skull 9 27 nbsp Schematic skull of a squamate showing the location of major dermal bones The group Squamata 17 includes snakes lizards and amphisbaenians Squamata can be characterized by the reduction or loss of limbs Snakes and legless lizards have evolved the complete loss of their limbs The upper jaw of Squamates is movable on the cranium a configuration called kinesis 28 This is made possible by a loose connection between the quadrate and its neighboring bones 29 Without this snakes would not be able consume prey that are much larger than themselves Amphisbaenians are mostly legless like snakes but are generally much smaller Three species of amphisbaenians have kept reduced front limbs and these species are known for actively burrowing in the ground 30 The tuatara and some extinct rhynchocephalians have a more rigid skull with a complete lower temporal bar closing the lower temporal fenestra formed by the fusion of the jugal and quadrate quadratojugal bones similar to the condition found in primitive diapsids However early rhynchocephalians and lepidosauromorphs had an open lower temporal fenestra without a complete temporal bar so this is thought to be a reversion rather than retention The temporal bar is thought to stabilise the skull during biting 31 Male squamates have evolved a pair of hemipenises instead of a single penis with erectile tissue that is found in crocodilians birds mammals and turtles The hemipenis can be found in the base of the tail The tuatara does not have a hemipenis but instead has shallow paired outpocketings of the posterior wall of the cloaca 16 nbsp The foot of a skink showing lepidosaurs characteristic overlapping scalesSecond most lepidosaurs have the ability to autotomize their tails However this trait has been lost on some recent species In lizards and rhynchoc fracture planes are present within the vertebrae of the tail that allow for its removal Some lizards have multiple fracture planes while others just have a single fracture plane The regrowth of the tail is not always complete and is made of a solid rod of cartilage rather than individual vertebrae 16 In snakes the tail separates between vertebrae and some do not experience regrowth 16 Third the scales in lepidosaurs are horny keratinized structures of the epidermis allowing them to be shed collectively contrary to the scutes seen in other reptiles 16 This is done in different cycles depending on the species However lizards generally shed in flakes while snakes shed in one piece Unlike scutes lepidosaur scales will often overlap like roof tiles Biology and ecology edit nbsp Python top and rattlesnake bottom featuring pit organs for infrared sensing Red arrows indicating pit organs and black arrows pointing to the nostrils Squamates are represented by viviparous ovoviviparous and oviparous species Viviparous means that the female gives birth to live young Ovoviviparous means that the egg will develop inside the female s body and Oviparous means that the female lays eggs A few species within Squamata have the ability to reproduce asexually 32 The tuatara lays eggs that are usually about one inch in length and which take about 14 months to incubate 28 While in the egg the Squamata embryo develops an egg tooth on the premaxillary that helps the animal emerge from the egg 33 A reptile will increase three to twentyfold in length from hatching to adulthood 33 There are three main life history events that lepidosaurs reach hatching birth sexual maturity and reproductive senility 33 Because gular pumping is so common in squamates and is also found in the tuatara it is assumed that it is an original trait in the group 34 Most lepidosaurs rely on camouflage as one of their main defenses Some species have evolved to blend in with their ecosystem while others are able to change their skin color to blend in with their current surroundings The ability to autotomize the tail is another defense that is common among lepidosaurs Other species such as the Echinosauria have evolved the defense of feigning death 33 Hunting and diet edit nbsp A green crested lizard feeding on an invertebrate Viperines can sense their prey s infrared radiation through bare nerve endings on the skin of their heads 33 Also viperines and some boids have thermal receptors that allow them to target their prey s heat 33 Many snakes are able to obtain their prey through constriction This is done by first biting the prey then coiling their body around the prey The snake then tightens its grip as the prey struggles which leads to suffocation 33 Some snakes have fangs that produce venomous bites which allows the snake to consume unconscious or even dead prey Also some venoms include a proteolytic component that aids in digestion 33 Chameleons grasp their prey with a projectile tongue This is made possible by a hyoid mechanism which is the contraction of the hyoid muscle that drives the tip of the tongue outwards 33 nbsp An eastern blue tongued lizard preyed upon by an eastern brown snake Within the subclass Lepidosauria there are herbivores omnivores insectivores and carnivores The herbivores consist of iguanines some agamids and some skinks 33 Most lizard species and some snake species are insectivores The remaining snake species tuataras and amphisbaenians are carnivores While some snake species are generalist others eat a narrow range of prey for example Salvadora only eat lizards 33 The remaining lizards are omnivores and can consume plants or insects The broad carnivorous diet of the tuatara may be facilitated by its specialised shearing mechanism which involves a forward movement of the lower jaw following jaw closure 35 While birds including raptors wading birds and roadrunners and mammals are known to prey on reptiles the major predator is other reptiles Some reptiles eat reptile eggs for example the diet of the Nile monitor includes crocodile eggs and small reptiles are preyed upon by larger ones 33 Conservation edit nbsp Global range of lizard species The geographic ranges of lepidosaurs are vast and cover all but the most extreme cold parts of the globe Amphisbaenians exist in Florida mainland Mexico including Baja California the Mediterranean region the Middle East North Africa sub Saharan Africa South America and the Caribbean 29 The tuatara is confined to only a few rocky islands of New Zealand where it digs burrows to live in and preys mostly on insects 28 Climate change has led to the need for conservation efforts to protect the existence of the tuatara This is because it is not possible for this species to migrate on its own to cooler areas Conservationists are beginning to consider the possibility of translocating them to islands with cooler climates 36 The range of the tuatara has already been minimized by the introduction of cats rats dogs and mustelids to New Zealand 37 The eradication of the mammals from the islands where the tuatara still survives has helped the species increase its population An experiment observing the tuatara population after the removal of the Polynesian rat showed that the tuatara expressed an island specific increase of population after the rats removal 38 However it may be difficult to keep these small mammals from reinhabiting these islands Habitat destruction is the leading negative impact of humans on reptiles Humans continue to develop land that is important habitat for the lepidosaurs The clear cutting of land has also led to habitat reduction Some snakes and lizards migrate toward human dwellings because there is an abundance of rodent and insect prey However these reptiles are seen as pests and are often exterminated 16 Interactions with humans edit nbsp Boots made from snake skin the three closest from diamondback rattlesnakes Snakes are commonly feared throughout the world Bounties were paid for dead cobras under the British Raj in India similarly there have been advertised rattlesnake roundups in North America Data shows that between 1959 and 1986 an average of 5 563 rattlesnakes were killed per year in Sweetwater Texas due to rattlesnake roundups and these roundups have led to documented declines and local extirpations of rattlesnake populations especially Eastern Diamondbacks in Georgia 16 People have introduced species to the lepidosaurs natural habitats that have increased predation on the reptiles For example mongooses were introduced to Jamaica from India to control the rat infestation in sugar cane fields As a result the mongooses fed on the lizard population of Jamaica which has led to the elimination or decrease of many lizard species 16 Actions can be taken by humans to help endangered reptiles Some species are unable to be bred in captivity but others have thrived There is also the option of animal refuges This concept is helpful to contain the reptiles and keep them from human dwellings However environmental fluctuations and predatorial attacks still occur in refuges 33 Reptile skins are still being sold Accessories such as shoes boots purses belts buttons wallets and lamp shades are all made out of reptile skin 16 In 1986 the World Resource Institute estimated that 10 5 million reptile skins were traded legally This total does not include the illegal trades of that year 16 Horned lizards are popularly harvested and stuffed 16 Some humans are making a conscious effort to preserve the remaining species of reptiles however References edit Jones Marc EH Anderson Cajsa Lisa Hipsley Christy A Muller Johannes Evans Susan E Schoch Rainer R 25 September 2013 Integration of molecules and new fossils supports a Triassic origin for Lepidosauria lizards snakes and tuatara BMC Evolutionary Biology 13 208 doi 10 1186 1471 2148 13 208 PMC 4016551 PMID 24063680 Pyron RA Burbrink FT Wiens JJ 2013 A phylogeny and revised classification of Squamata including 4 161 species of lizards and snakes BMC Evolutionary Biology 13 93 doi 10 1186 1471 2148 13 93 PMC 3682911 PMID 23627680 Uetz Peter 13 January 2010 The original descriptions of reptiles Zootaxa 2334 1 59 68 doi 10 11646 zootaxa 2334 1 3 Jones M E H 2009 Dentary Tooth Shape in Sphenodon and Its Fossil Relatives Diapsida Lepidosauria Rhynchocephalia Frontiers of Oral Biology 13 9 15 doi 10 1159 000242382 ISBN 978 3 8055 9229 1 PMID 19828962 Hay Jennifer M Sarre Stephen D Lambert David M Allendorf Fred W Daugherty Charles H June 2010 Genetic diversity and taxonomy a reassessment of species designation in tuatara Sphenodon Reptilia Conservation Genetics 11 3 1063 1081 doi 10 1007 s10592 009 9952 7 hdl 10072 30480 S2CID 24965201 Jones M E H Cree A 2012 Tuatara Current Biology 22 23 986 987 doi 10 1016 j cub 2012 10 049 PMID 23218010 Evans S E Jones M E H 2010 The Origin early history and diversification of lepidosauromorph reptiles In Bandyopadhyay S ed New Aspects of Mesozoic Biodiversity Lecture Notes in Earth Sciences Vol 132 pp 27 44 doi 10 1007 978 3 642 10311 7 2 ISBN 978 3 642 10310 0 Simoes T R Kammerer C F Caldwell M W Pierce S E 2022 Successive climate crises in the deep past drove the early evolution and radiation of reptiles Science Advances 8 33 eabq1898 doi 10 1126 sciadv abq1898 PMC 9390993 PMID 35984885 a b Ford David P Evans Susan E Choiniere Jonah N Fernandez Vincent Benson Roger B J 2021 08 25 A reassessment of the enigmatic diapsid Paliguana whitei and the early history of Lepidosauromorpha Proceedings of the Royal Society B Biological Sciences 288 1957 20211084 doi 10 1098 rspb 2021 1084 ISSN 0962 8452 PMC 8385343 PMID 34428965 Sues Hans Dieter Schoch Rainer R 2023 11 07 The oldest known rhynchocephalian reptile from the Middle Triassic Ladinian of Germany and its phylogenetic position among Lepidosauromorpha The Anatomical Record doi 10 1002 ar 25339 ISSN 1932 8486 PMID 37937325 S2CID 265050255 Simōes Tiago R Caldwell Michael W Talanda Mateusz Bernardi Massimo Palci Alessandro Vernygora Oksana Bernardini Federico Mancini Lucia Nydam Randall L 30 May 2018 The origin of squamates revealed by a Middle Triassic lizard from the Italian Alps Nature 557 7707 706 709 Bibcode 2018Natur 557 706S doi 10 1038 s41586 018 0093 3 PMID 29849156 S2CID 44108416 Rage Jean Claude December 2013 Mesozoic and Cenozoic squamates of Europe Palaeobiodiversity and Palaeoenvironments 93 4 517 534 doi 10 1007 s12549 013 0124 x ISSN 1867 1594 S2CID 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Reptile Phylogeny and Reveal Unexpected Placements for Fossil Taxa PLOS ONE 10 3 e0118199 Bibcode 2015PLoSO 1018199R doi 10 1371 journal pone 0118199 PMC 4372529 PMID 25803280 Rieppel O DeBraga M 1996 Turtles as diapsid reptiles PDF Nature 384 6608 453 5 Bibcode 1996Natur 384 453R doi 10 1038 384453a0 S2CID 4264378 Muller Johannes 2004 The relationships among diapsid reptiles and the influence of taxon selection PDF In Arratia G Wilson M V H Cloutier R eds Recent Advances in the Origin and Early Radiation of Vertebrates Verlag Dr Friedrich Pfeil pp 379 408 ISBN 978 3 89937 052 2 Mannen Hideyuki Li Steven S L Oct 1999 Molecular evidence for a clade of turtles Molecular Phylogenetics and Evolution 13 1 144 148 doi 10 1006 mpev 1999 0640 PMID 10508547 Zardoya R Meyer A 1998 Complete mitochondrial genome suggests diapsid affinities of turtles Proc Natl Acad Sci U S A 95 24 14226 14231 Bibcode 1998PNAS 9514226Z doi 10 1073 pnas 95 24 14226 ISSN 0027 8424 PMC 24355 PMID 9826682 Iwabe N Hara Y Kumazawa Y Shibamoto K Saito Y Miyata T Katoh K 2004 12 29 Sister group relationship of turtles to the bird crocodilian clade revealed by nuclear DNA coded proteins Molecular Biology and Evolution 22 4 810 813 doi 10 1093 molbev msi075 PMID 15625185 Roos Jonas Aggarwal Ramesh K Janke Axel Nov 2007 Extended mitogenomic phylogenetic analyses yield new insight into crocodylian evolution and their survival of the Cretaceous Tertiary boundary Molecular Phylogenetics and Evolution 45 2 663 673 doi 10 1016 j ympev 2007 06 018 PMID 17719245 Katsu Y Braun E L Guillette L J Jr Iguchi T 2010 03 17 From reptilian phylogenomics to reptilian genomes analyses of c Jun and DJ 1 proto oncogenes Cytogenetic and Genome Research 127 2 4 79 93 doi 10 1159 000297715 PMID 20234127 S2CID 12116018 Tyler R Lyson Erik A Sperling Alysha M Heimberg Jacques A Gauthier Benjamin L King Kevin J Peterson 2012 02 23 MicroRNAs support a turtle lizard clade Biology Letters 8 1 104 107 doi 10 1098 rsbl 2011 0477 PMC 3259949 PMID 21775315 Evans S E 2003 At the feet of the dinosaurs the early history and radiation of lizards PDF Biological Reviews 78 4 513 551 doi 10 1017 S1464793103006134 PMID 14700390 S2CID 4845536 Archived from the original PDF on 2019 02 19 Evans Susan E 2016 Clack Jennifer A Fay Richard R Popper Arthur N eds The Lepidosaurian Ear Variations on a Theme Evolution of the Vertebrate Ear vol 59 Cham Springer International Publishing pp 245 284 doi 10 1007 978 3 319 46661 3 9 ISBN 978 3 319 46659 0 retrieved 2024 01 08 a b c Bellairs Angus d A 1960 Reptiles life history evolution and structure Harper OCLC 692993911 page needed a b Benton M J 1988 The Phylogeny and classification of the tetrapods Oxford OCLC 681456805 page needed Vidal Nicolas Hedges S Blair February 2009 The molecular evolutionary tree of lizards snakes and amphisbaenians Comptes Rendus Biologies 332 2 3 129 139 doi 10 1016 j crvi 2008 07 010 PMID 19281946 S2CID 23137302 Simoes Tiago R Kinney Broderick Grace Pierce Stephanie E 2022 03 03 An exceptionally preserved Sphenodon like sphenodontian reveals deep time conservation of the tuatara skeleton and ontogeny Communications Biology 5 1 195 doi 10 1038 s42003 022 03144 y ISSN 2399 3642 PMC 8894340 PMID 35241764 Smith James G 2010 Survival estimation in a long lived monitor lizard radio tracking of Varanus mertensi Population Ecology 52 243 247 doi 10 1007 s10144 009 0166 0 S2CID 43055329 a b c d e f g h i j k l m Zug George R 1993 Herpetology An Introductory Biology of Amphibians and Reptiles Academic Press ISBN 978 0 12 782620 2 page needed Functional morphology and evolution of aspiration breathing in tetrapods Jones M E H O Higgins P Fagan M Evans S E Curtis N 2012 Shearing mechanics and the influence of a flexible symphysis during oral food processing in Sphenodon Lepidosauria Rhynchocephalia The Anatomical Record 295 7 1075 1091 doi 10 1002 ar 22487 PMID 22644955 S2CID 45065504 Besson A A Cree A 2011 Integrating physiology into conservation an approach to help guide translocations of a rare reptile in a warming environment Animal Conservation 14 28 37 doi 10 1111 j 1469 1795 2010 00386 x S2CID 84015883 Nelson Nicola J et al 2002 Establishing a new wild population of tuatara Sphendon guntheri Conservation Biology 16 4 887 894 doi 10 1046 j 1523 1739 2002 00381 x S2CID 85262510 Towns David R 2009 Eradication as reverse invasion lesions from Pacific Rat Rattus exulans removals on New Zealand islands Biol Invasions 11 7 1719 1733 doi 10 1007 s10530 008 9399 7 S2CID 44200993 External links edit nbsp Reptiles portal Animaldiversity ummz umich edu Reptile taxonomy Benton 2004 Lepidosaur phylogeny Retrieved from https en wikipedia org w index php title Lepidosauria amp oldid 1218719363, wikipedia, wiki, book, books, library,

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