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The present study is a review of the 1976 publication by professor A.D. NIAZI, director of the Natural History Museum of Bagdad, on the Lacertini of Iraq, including additional materials from Irqi collections. Twenty-two individuals of five taxa of this group originating from the territory under study were indentified in Iraqi collections: Lacerta cf. strigata EICHWALD, 1831 which had been removed from the list of Iraqi lacertids by many authors, L. media media LANTZ & CYRÉN, 1920, Timon kurdistanicus (SUCHOW, 1936) and two subspecies of Apathya cappadocica (WERNER, 1902). A key for identification and a map of the records are also presented.

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The Northwest of Iran, covering the three provinces of Ardabil, East Azerbaijan and West Azerbaijan, is a special area that, due to its particular geographical and climatic conditions has a rich biodiversity. The present study was conducted with the aim of studying the habitat, substrate type, feeding, conservation and distribution of lizards in this area from 2003 to now. Our results have revealed that there are 20 lizard species belonging to 13 genera and 5 families in this area. Lacertid lizards have the highest species diversity with 12 species. We also found that high ranges of habitats with a different substrate types are inhabited by lizard species. The number of species in pine regions compared with other types of area is considerably greater. The conservation status of lizards is unknown and requires further study.

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Anhand ihrer Feld- und Literaturstudien identifizierten die Autoren 36 Amphibien- und Reptilienarten, die nachweislich in der turkischen Provinz Bitlis vorkommen, wobei die Fundorte und die an ihnen angetroffenen Habitattypen angegeben werden. die durch Beobachtung festgestellten Hauptgefahrdungsursachen werden benannt. insgesamt kennt man aus dem Untersuchungsgebiet Vorkommen von vier Froschlurch-, zwei Schwanzlurch- und Schildkrötenarten sowie 15 Echsen- und 13 Schlangenarten. Hyla savignyi Audouin, 1827, Heremites vittatus (Olivier, 1804), Timon kurdistanicus (Suchow, 1936) and Eirenis thospitis Schmidtler & Lanza, 1990, stellen Erstnachweise fur die Provinz Bitlis dar.

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The present work provides a list of all amphibians and reptiles recorded from Iraq up to 2014. It includes 115 species (105 species of reptiles and 10 species of amphibians) dating back to 25 families (20 families of reptiles and 5 families of amphibians). Conservation status of each species was mentioned.

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An extensive review on the taxonomic status, occurrence, geographical distribution, and the IUCN conservation status of 122 species/taxa (10 amphibians and 112 reptiles) belonging to 71 genera (8 genera of amphibians and 63 of reptiles) and to 25 families (5 families of amphibians and 20 families of reptiles) was made. As a part of Iraq’s unique biota, the knowledge of the herpetofauna of Iraq is poorly discovered and requires extensive field surveys, further research, and explorations in order to create full frame knowledge of its status and conservation.

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Acanthodactylus cantoris blanfordi, Acanthodactylus cantoris schmidti, Acanthodactylus fraseri, Acanthodactylus micropholis, Apathya cappadocica urmiana, Eremias arguta, Eremias brevirostris, Eremias fasciata, Eremias grammica, Eremias guttulata, Eremias intermedia, Eremias lineolata, Eremias nigrocellata, Eremias persica, Eremias pleskei, Eremias scripta, Eremias strauchi, Eremias velox velox, Lacerta brandtii, Lacerta chlorogaster, Lacerta princeps princeps, Lacerta princeps kurdistanica, Lacerta saxicola defilippii. Lacerta saxicola raddei, Lacerta strigata, Lacerta trilineata media, Ophisops elegans.

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Acanthodactylus blanfordi, Acanthodactylus boskianus, Acanthodactylus grandis, Acanthodactylus micropholis, Acanthodactylus nilsoni, Acanthodactylus opheodurus, Acanthodactylus schmidti, Eremias acutirostris, Eremias andersoni, Eremias arguta, Eremias fasciata, Eremias grammica, Eremias intermedia, Eremias lalezharica, Eremias lineolata, Eremias nigrocellata, Eremias nigrolateralis, Eremias persica, Eremias pleskei, Eremias scripta, Eremias strauchi strauchi, Eremias strauchi kopetdaghica, Eremias velox velox, Lacerta brandtii, Lacerta cappadocica urmiana, Lacerta chlorogaster, Lacerta defilippii, Lacerta media media, Lacerta mostoufi, Lacerta praticola praticola, Lacerta princeps princeps, Lacerta princeps kurdistanica. Lacerta raddei raddei, Lacerta raddei vanensis, Lacerta steineri, Lacerta strigata, Lacerta valentini valentini, Lacerta zagrosica, Mesalina brevirostris brevirostris, Mesalina brevirostris fieldi, Mesalina watsonana, Ophisops elegans.

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The present study is on the morphologies and sizes of peripheral blood cells (erythrocytes, leukocytes, and thrombocytes) on blood smears, stained with Wright`s stain, in some lacertid lizards species [Apathya cappadocica (Werner, 1902), Acanthodactylus boskianus (Daudin, 1802), Acanthodactylus harranensis Baran et al. 2005, Anatolacerta danfordi (Günther, 1876), Darevskia praticola (Eversmann, 1834), D. uzzelli (Darevsky and Danielyan, 1977), D. valentini (Boettger, 1892), Parvilacerta parva (Boulenger, 1887), Lacerta pamphylica Schmidtler, 1975, L. trilineata Bedriaga, 1886, L. viridis (Laurenti, 1768), Ophisops elegans Menetries, 1832, Mesalina brevirostris Blanford, 1876, Podarcis muralis (Laurenti, 1768), P. sicula (Rafinesque-Schmaltz, 1810), Timon princeps (Blanford, 1874)] from Turkey. As a result of our survey, it was determined that the blood cells of the investigated species are shows significant variations in sizes and of leukocytes, agranulocytic leukocytes (lymphocytes and monocytes) are present as predominant cells. Moreover, of granulocytes, neutrophils were no observed in A. danfordi, D. praticola, D. uzzelli, and P. parva.

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Algyroides fitzingeri, Algyroides marchi, Algyroides moreoticus, Algyroides nigropunctatus, Lacerta agilis, Lacerta lepida, Lacerta princeps, Lacerta schreiberi, Lacerta strigata, Lacerta trilineata, Lacerta viridis, Lacerta andreanszkyi, Lacerta armeniaca, Lacerta bedriagae, Lacerta brandtii, Lacerta cappadocica, Lacerta caucasica, Lacerta chlorogaster, Lacerta cyanura, Lacerta danfordi, Lacerta derjugini, Lacerta dugesii, Lacerta fraasii, Lacerta graeca, Lacerta horvathi, Lacerta jayakari, Lacerta laevis, Lacerta monticola, Lacerta mosorensis, Lacerta oxycephala, Lacerta parva, Lacerta perspicillata, Lacerta praticola, Lacerta rudis, Lacerta saxicola, Lacerta vivipara, Gallotia atlantica, Gallotia galloti, Gallotia simonyi, Podarcis erhardii, Podarcis filfolensis, Podarcis hispanica, Podarcis lilfordi, Podarcis melisellensis, Podarcis milensis, Podarcis muralis, Podarcis peloponnesiaca, Podarcis pityusensis, Podarcis sicula, Podarcis taurica, Podarcis tiliguerta, Podarcis wagleriana, Psammodromus algirus, Psammodromus blanci, Psammodromus hispanicus, Psammodromus microdactylus.

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The basic anatomy of the lacertid hemipenis (intromittent organ) and methods for its investigation are described. In many members of the Lacertidae, the hemipenis has a structure quite unlike that of other squamate reptiles: the distal lobes of the retracted organ are complexly folded and there is a well-defined supporting structure of dense connective tissue, the armature. This incorporates blood sinuses and has an intramuscular portion embedded in the m. retractor penis magnus and two club-shaped bodies, the clavulae, that support the lobes in the erect organ. Unarmatured hemipenes occur in some lacertids and, like those of other squamates, possess sac-like lobes in the retracted state, but they are singular in having the lobes invested by the m. retractor penis magnus. It is argued that many of these apparently primitive hemipenes are in fact secondary derivatives of the armatured type. There is considerable inter-specific variation in hemipenial structure which is described systematically. In some cases this involves differences in size, asymmetry and simplification, which may arise as physical isolating mechanisms and is useful in distinguishing otherwise very similar species, particularly in the genus Mesalina (p. 1253). Other shared derived hemipenial features provide useful information about relationships between species and higher taxa and a summary of the hypotheses that they support is given (p. 1254).

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Relationships of lacertid lizards were assessed on the basis of 84 primary and 112 binary characters drawn mainly from morphology, including features of the skeleton, external anatomy, various internal soft part systems and two aspects of behaviour. Among features not previously used, or not fully investigated before, are structure of the septomaxilla and nasal passages, arranged of the xiphisternal cartilages, mite pockets, kidney position, ulnar nerve arragement, thoracic fascia, aspects of the hemipenis and its associated muscles, female genitalia and jaw muscles. On the basis of parsimony analysis and compatibilty treatment of this character set, the Lacertidae fall into two main portions: A paraphyletic Palaearctic and Oriental group of primitive forms, from which is derived a holophyletic assemblage of Ethiopian and advanced Saharan and Eurasian taxa. The former group ist not fully resolvable, but Psammodromus and Gallotia appear to be sister groups and are probably related to Lacerta parva and L. fraasi and then L. brandtii, Podarcis appears to be related successively to L. andreanszkyi, the sister species L. dugesii and L. perspicillata, and perhaps L. danfordi and L. laevis. This assemblage may be related to archaeolacertas and Algyroides. The separation of Lacerta lepida, L. pater and L. princeps from the agilis group, based on chemical evidence, is weakly contradicted by morphology. Takydromus may be most closely related to L. vivipara, and L. jayakari and L. cyanura constitute the most likely sister group of the Ethiopian and advanced Saharo-Eurasian assemblage. Taxe in the Ethiopian and advanced SaharoEuroasian assemblage form a long essentially pectinate tree with relatively change between the side branches, except for a strong disjunction separating the more primitive from the more advanced taxa. Most of the former fall on two main branches, with ´Lacerta` australis and ´L.` rupicola possibly basal to them. 1. the Equatorial forest group containing Gastropholis, Bedriagaia, ´Lacerta` echinata, Adolfus, ´Lacerta` jacksoni and Holaspis. The first three of these constitute a holophyletic group and the same is probably true of the remainder. 2. Tropidosaura, Poromera and Nucras, the latter being the sister group of the more advanced forms. These include successively the Ethiopian Philochortus, Latastia, Ichnotropis and Heliobolus, Pseuderemias, Meroles and Aporosaura, and Pedioplanis, and then the Saharo-Eurasian Eremias, Acanthodactylus, Mesalina and Ophisops-Cabrita. It seems probable that the ancestors of modern Lacertidae arose in western Eurasia, where the family is known since the Palaeocene and is still represented there largely by quite primitive forms (89 species and seven nominal genera). The family later invaded Africa, perhaps first in the early or middle Miocene. Relatively primitive lacertids spread widely in largely mesic situations in the Ethiopian region, radiating to some extent (six present genera and 16 species) and producing Nucras and the related series of advaned groups (eight genera and 54 species) whoich show increasing adaptation to xeric environments. These genera tend to have heir most primitive species in the northeast and north of the Ethiopian region. The most advaned gave rise to the Saharo-Eurasian clade, now made up to Eremias, Acanthodactylus, Mesalina and Ophisops-Cabrita. This invaded the arid areas of North Africa and Eurasia, where it is presently represented by 70 species. Many morphological changes in increasingly advanced lacertids may be functionally related to the problems of survival in arid, hot, open environments. Considerable ecological parallelism exists in lacertids, with members of separate stocks occupying similar niches in different geographical areas. Morphological adaptations associated with these niches contribute significantly to the high levels of character homoplasy found in the family. There is also some correlation between the degree of niche differentiation in various groups and the quality of the phylogenies that can be produced from their physical characters. A number of morphological parallels exist between advaned lacertids and New World macroteiids. In the skull at least, advaned lacertids show a complex mixture of paedomorphosis and acceleration. Nomenclatorial changes are as follows: Cabrita is synonymised with Ophisops, necessitating a new name, Ophisops nictans, for Cabrita jerdonii. Aporosaura is synonymised with Meroles, Platyplacopus with Takydromus, and Bedriagaia with Gastropholis. ´Lacerta` (or Centromastyx) echinata is also transferred to the latter genus and Lacerta jacksoni to Adolfus. ´Lacerta` australis and ´L.` rupicola are put in a new genus, Australolacerta. It is recommended that Lacerta dugesii and L. perspicillata should not be placed in the otherwise very uniform genus Podarcis. Although clearly paraphyletic, Lacerta s. lat. Should be retained at least for the present and, if necessary putative relationships within it indicated by informal groups or subgenera.

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Estimates of phylogeny may allow historical events to be reconstructed even without a fossil record. The reliability of such interpretations depends not only on the robustness of the phylogeny but also on its topology. Changes in individual features can be traced and general histories of groups developed and compared with each other. Results are ofter surprising, for Instance the sophisticated tail shedding mechanism of lizards turns out to be a primitive feature that has been lost many times. Similarly, ecological analogues may have developed their common characaters in quite different orders. Phylogenies also provide a way of recognizing constraints and the effects of history on present ecological and behavioural patterns. When using anatomical characters the quality of the apparent phylogenies produced may be related to ecological history: expansion of a group along an ecological continuum into increasingly demanding niches ina small geographical area tends to produce a robust phylogeny (for instance in Meroles), while this is often not so for widely distributed groups that occupy a more modest range of niches (such as Pedioplanis and Podarcis). Non-morphological data may not show this tendency, but can have their own problems. Lacertids can be referred to clade with many successive branches in Africa and the Saharo-Eurasian arid zones and a less resolved probably paraphyletic complex of more primitive forms in the Mediterranean and wider Palaearctic areas. The African-Eurasian clade shows a general trend towards ground-dwelling and increasingly arid habitats but is ecologically variied. These animals are important to the study of Mediterranean forms because they provide eco-morphological parallels to them (for instance to Algyroides, Psammodromus and the archaeolacertas) and help form a basis for testing hypotheses about function. Although it is possible to recognise a number of distinct clades among the Mediterranean and Eurasian forms, relationships within and between these are often much less well substantiated. If results are available in time, current work on mitochondrial DNA sequencing will be discussed.

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DNA sequence indicates the Lacertidae contain two subfamilies, Gallotiinae and Lacertinae, the latter comprising two monophyletic tribes, the Eremiadini of Africa and arid southwest and central Asia, and the Lacertini of Europe, northwest Africa and southwest and east Asia. Relationships within the 108 species of Lacertini are explored using mtDNA (291 bp cytochrome b; 329 bp 12S rRNA for 59 nominal species, and reanalysis of the data of Harris et al. 1998, and Fu 2000). The morphology of the tribe is reviewed and 64 of its characters (equivalent to 83 binary ones) also used to assess relationships. The Lacertini are assigned to 19 monophyletic units of 1 to 27 species, recognised here as the following genera (contents are indicated in brackets): Algyroides, Anatololacerta gen. nov. (L. danfordi group), Apathya (L. cappadocica group), Archaeolacerta (L. bedriagae), Dalmatolacerta gen. nov. (L. oxycephala), Darevskia (L. saxicola group), Dinarolacerta gen. nov. (L. mosorensis), Hellenolacerta gen. nov. (L. graeca), Iberolacerta (L. monticola group), Iranolacerta gen. nov. (L. brandtii and L. zagrosica), Lacerta s. str. (sand and green lizards, L. agilis group), Parvilacerta gen. nov. (L. parva and L. fraasii), Phoenicolacerta gen. nov. (L. laevis group), Podarcis (wall lizards), Scelarcis (L. perspicillata), Takydromus (Asian grass lizards), Teira (L. dugesii), Timon (ocellated lizards, L. lepida group) and Zootoca (L. vivipara). Both mtDNA and morphology indicate that Lacerta and Timon are sister taxa, and DNA suggests further possible relationships among genera (Fig. 1, p. 6). Neither DNA nor morphology indicates that the archaeolacertas (sometimes formalised as Archaeolacerta sens. lat.) form a clade. Instead, they are representatives of an ecomorph associated with living on rock exposures and using the narrow crevices that these contain. The Lacertidae probably arose in the European area, with the Gallotiinae later reaching Northwest Africa and the Canary Islands, and the ancestor of the Eremiadini invading Africa in the mid-Miocene. The Lacertini spread through much of their present European range and diversified, perhaps largely by repeated vicariance, around 12–16 My ago, producing the ancestors of the present mainly small-bodied genera, which then underwent often modest speciation. Three units spread more widely: the Lacerta-Timon clade of large-bodied lizards probably dispersed earliest, followed by Algyroides and then Podarcis. Overall, European Lacertidae show a pattern of repeated spread, often accompanied by restriction of previous groups. Expansion of Lacertini may have displaced earlier lacertid lineages from all or much of Europe; while spread of Podarcis may have restricted many other genera of Lacertini. The earlier expansion of the Lacerta-Timon clade probably did not have this effect, as difference in adult body size restricted competitive interaction with other forms. Several invasions of more distant areas also occurred: of East Asia by Takydromus over 10 My ago, and more recently of northwest Africa by Podarcis, Scelarcis and Timon, and Madeira by Teira. Relationships within the Eremiadini estimated from both mtDNA, and nDNA differ considerably from those based on morphology. They indicate relatively mesic forms may have diversified widely across Africa and given rise to at least three independent invasions of arid habitats. MtDNA also indicates that Lacerta andreanskyi belongs in the Eremiadini and may occupy a basal position there. It is assigned to a further new genus, Atlantolacerta gen. nov.

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Die Pyrenäenarten von Archaeolacerta s.l. (A. aranica, A. aurelioi und A. bonnali) unterscheiden sich von den übrigen Arten der Eurasiatischen Radiationslinie (sensu MAYER & BENYR 1994) durch den Besitz knöcherner Rippen im Bereich des dritten Präsakralwirbels. Die drei Pyrenäenarten zeigen in der Morphologie von Postorbitale und Postfrontale jeweils osteologische Verschiedenheiten, die Artniveau erreichen und ihre zweifelsfreie Unterscheidung erlauben. Auch finden sich Unterscheidungsmerkmale im Schultergürtel (Klavikel und Sternalfontanella). Apomorphe Merkmale innerhalb der kaukasischen ´Lacerta` saxicola – Gruppe stellen deutliche Unterschiede sowohl gegenüber den Archaeolacerten Europas (fast immer einzusätzlicher Präsakralwirbel) als auch gegenüber Apathya (ein zusätzlicher Präsakralwirbel und eine verminderte Anzahl von Prämaxillarzähnen) dar. ´L.` chlorogaster unterscheidet sich von den übrigen kaukasischen Formen klar durch die Zahl der Prämaxillarzähne und Form der Interklavikel. Die parthenogenetischen Taxa zeigen deutliche Ähnlichkeiten (Modalwerte der Wirbelzahl, Morphologie des Postorbitale) zu ihrem Elternarten, besonders zur weiblichen Elternart. Aufgrund der osteologischen Befunde wird deutlich, daß die europäischen, vorläufig in der Sammelgattung Archaeolacerta s.l. vereinigten Taxa keine natürliche Einheit darstellen. Die Formen der Pyrenäen und des Kaukasus erscheinen osteologisch deutlich differenziert, während die iberischen, balkanischen und tyrrhenischen Taxa in den untersuchten Strukturen nur synplesiomorphe Merkmalsausprägungen gemeinsam haben, die keine Aussagen über ihre Verwandtschaft ermöglichen.

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Archaeolacerta s. l., in the currently utilized sense results to be a polyphyletic taxon, composed of three monophyletic and phylogenetically well differentiated taxa: a)-Archaeolacerta (s. str.) Mertens, 1921, which includes three species: A. bedriagae, A. oxycephala, and A. mosorensis, distributed by the northern part of the Central Mediterranean (Corsica, Sardinia, and west Balcanic Peninsula). His most related genera seem to be Teira (his adelphotaxon in our study), Apathya, and Omanosaura. b)-Iberolacerta gen. nov., with two subgenera: Iberolacerta s. str. and Pyrenesaura subgen. nov. includes six species: I. monticola, I. cyreni, I. bonnali, I. aranica, I. aurelioi, and I. horvathi. They are distributed by the mountains of Western Europe (Iberian Peninsula, Pyrenees, Central and Eastern Alps and the north of the Dinaric Chains). His adelphotaxon are the Caucasian and Near East species of Darevskia gen. nov. c)-The third taxa is Darevskia gen. nov., which includes the species of the `L.` saxicola complex besides `L.` derjugini, `L.` praticola, and `L.` chlorogaster. They are distributed by Eastern Europe, Caucasus, and Near East. Other clear relationships among some taxa of the Eurasian Radiation [= `Eurasische linie` from (Mayer and Benyr, 1994)] have been found: Algyroides seems to be the sister group of the species considered of uncertain phylogenetic relationships belonging to the `L.` danfordi-laevis group and of Podarcis. `L.` brandtii seems to be a very primitive species within the Eurasian Radiation. Omanosaura and Apathya appear as sister taxa. `L.` graeca occupies a very basal position in the sister group of Podarcis and relatives (see above). `L.` andreanskyi is the sister species of the Darevskia nov. and Iberolacerta nov. clade. The assimilation of `L.` andreanskyi to Teira is very problematic. Also the `L.` parva group seems to be related to Timon. Some groups of species like `L.` brandtii, `L.` parva-fraasii and `L.` danfordi-laevis probably merit generic rank, but it is necessary a more deep study before to take a decision.

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The microornamentation of the scales (oberhautchen) has been studied by means of enamel casts (in negative), or with detached skin pieces (positive cast in the upper face or negative in their lower face of the scales) and its observation by transparency with optical microscopy at 40x, 400x and 1000x. In this study we have found a remarkable uniformity in all genera of Lacertini studied (already known, although significantly expanding the number of species previously studied). In light of the results obtained, it seems that the use of the microornamentation of the scales in taxonomy is limited. There is a remarkable degree of variation and probably of homoplasy, as it happens in so many characters of Lacertini. Nor is it clearly linked to certain conditions of the environment, although it may have a certain importance in mechanisms such as evapotranspiration and perhaps in the crypsis through its influence on the reflectance of the scales. These scales can present protuberances (like small tubercles) on their surface (derived character) in Algyroides (the four species), and in the case of Algyroides marchi also seems to present small pits on its scale surface. In most lacertids the cells of the “oberhautchen” are usually narrow (or short anteroposteriorly, if preferred), between 1 and 4 μm, having the appearance of ribbons or transverse straps. Smaller sizes (derivated) appear more or less marked in Algyroides spp, Darevskia praticola complex, Parvilacerta spp and in Dinarolacerta mosorensis (although not in D. montenegrina) and is difficult to interpret. Except in Dinarolacerta, in the other species it coincides that they are ground or ground-rock interface species, and the coarser stripes could have to do with reflectance (imitating the vegetation or the medium between which they move, according to the hypothesis of Allam et al.). In the case of Dinarolacerta, very saxicolous, it is probably the sister group of Algyroides and the common morphology could have a phylogenetic origin linked to its relationship with Algyroides. There is also no relationship with moisture since some come from dry places and others are from very wet areas. The posterior flange of the cells may be slightly mounted in the next cell (primitive character) but appears quite raised (derived character) in Algyroides nigropunctatus (much less in A. moreoticus and A. marchi, and apparently little or nothing in A. fitzingeri). The rear flange of the cells can be smooth, corrugated or notched. In our samples, irregular (and even dentate) posterior ridges appear in numerous Darevskia such as D. derjugini, D. parvula, D. raddei complex [D. raddei raddei, D. r. vanensis and D. nairensis], in part of the group of D. rudis [D. rudis sspp. and D. bithynica sspp.], several Iberolacerta (I. bonnali, I. horvathi and I. monticola astur), as well as in Teira dugesii. The character appears, although less marked in Algyroides (more in A. moreoticus, but less marked or barely visible in the others), in Hellenolacerta graeca, and other Iberolacerta (I. aurelioi, I. martinezricai, and scarcely marked in I. cyreni). Very little marked in Darevskia mixta, somewhat more in D. dryada and none in D. clarkorum, and also appears in the group of D. saxicola (D. saxicola, D. brauneri brauneri, D. b. darevskii, D. lindholdmi, D. szczerbaki), Dalmatolacerta oxycephala, Dinarolacerta mosorensis (only in the Biokovo sample, and not in Durmitor or D. montenegrina), Apathya cappadocica, in some places of the scales of Parvilacerta fraasii (but not in P. parva) and very little in D. (p) hungarica; also in the remaining group of D. rudis (D. valentini valentini, D. v. lantzicyreni, D. rudis bolkardaghica, D. portschinskii), and some parthenogenetic species (D. armeniaca, D. dahli, D. rostombekowi) but not in D. unisexualis, D. uzzelli, D. sapphirina, D. bendimahiensis or in the triploid hybrid between D. unisexualis and D. nairensis. In these parthenogenetic species it seems a general rule that the character of the crenulation or irregularity of the posterior flange of the cells resembles that of the paternal rather than the maternal species. The exception is the triploid hybrid [arisen from the hybridization of D. unisexualis (parthenogenetic female, without the character) and a male of D. nairensis (with fairly developed character)] that lacks character, and in this case is more similar to the maternal species of which has two genetic sets compared to only one of the paternal one.

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The first record of the lacertid lizard Apathya cappadocica muhtari from Iran is presented based on five specimens (four males and one female) collected from June to August 2011 from 40 km southwest of Bane, Kurdistan province, western Iran. The specimens were examined based on morphometrics, color pattern and pholidotic characters. The most distinguishing characters of A. c. muhtari are the presence of an undivided and single preanal plate and six longitudinal rows of ventral shields.

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A complete catalogue is provided for the type specimens of lacertid lizards in the herpetological collection of the Zoological Museum, Berlin, as of December, 1993. The collection contains a total of 514 type specimens, representing 63 taxa, of which 42 are currently regarded as valid at the specific or subspecific level. Types representing an additional four taxa appear to have been lost from the collection. The collections are especially rich in African lacertid types and in historically significant specimens collected early in the Nineteenth Century by Pallas, Eversmann, and Hemprich & Ehrenberg. Also present are the type series of many subspecies of Podarcis lilfordi and P. pityusensis described by Eisentraut.

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A total of thirty-one Anatolian Lizard, Apathya cappacocica, samples from several provinces of Eastern and South-Eastern Turkey were examined for helminths. Two species of Nematoda, including Spauligodon atlanticus, Skrjabinodon medinae; two species of Cestoda, including Mesocestoides sp. tetrahydia and Oochoristica tuberculata and one species of Acanthocephala, Centrorhynchus sp. were found. This is the first helminth record of A. cappodocica from Turkey. A. cappadocica represents a new host record for each of the parasite species. S. atlanticus is reported from Turkey for the fi rst time.

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GEORGI FEDOROWITSCH SUCHOW (1899-1942) was one of those researchers from the former Soviet Union who has been completely forgotten. This changed with the memories of his daughter NATALIA GEORGIEVNA SUKHOVA, published in 2015. Born in Ukraine, SUKHOV went to Leningrad in 1930, but did not get the hoped-for position as a scientist in the local herpetological department of the Zoological Museum of the Academy of Sciences of the USSR. He was only hired as a museum guide. In February 1942 he died as a result of the siege of Leningrad by German troops. SUCHOW’S twelve herpetological works were almost exclusively devoted to the lacertid lizards. He described five new taxa, four of which are valid (Lacerta agilis tauridica, Lacerta agilis boemica, Apathya cappadocica urmiana und Timon kurdistanicus).

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During two excursions to Syria (March/April and May 1994) 9 species of lacertid lizards were found (Acanthodactylus grandis, A. orientalis, A. tristrami, Lacerta media wolterstorffi L. cappadocica wolteri, L. l. laevis, L. (cf.) kulzeri, Mesalina brevirostris and Ophisops elegans ssp.). Three of them (A. tristrami, L. cappadocica wolteri and L. (cf.) kulzeri) are reported for the first time for this country. Concerning L. cappadocica, L. laevis, L. (cf.) kulzeri and O. elegans systematical questions are discussed. Ecological data are presented. Further amphibians and reptiles found during the excursions are listed, Coluber najadum is reported for the first time for Syria.

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In the herpetological collection of ZFMK 528 scientific species group names are represented by type materi- al. Of these, 304 names are documented by primary type specimens (onomatophores) while for 224 further names sec- ondary type specimens (typoids) are available, ranging chronologically from 1801 to 2010. The list is a shortened pred- ecessor of a comprehensive type catalogue in progress. It lists name bearing types with their catalogue numbers includ- ing information on further type series members also in other institutions, while secondary types are listed only by pres- ence, both in ZFMK and other collections including holotype repositories. Geographic origin and currently valid names are also provided.

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The physical geography of Iraq is summarised. Using data from the relevant literature and current information from the Internet, a very provisional checklist of Iraqi amphibians and reptiles is presented. Ten amphibian species are reported for Iraq, and exactly 100 reptile species.

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The interspecific relationships among female size, clutch size, egg size, and hatchling size were examined for 64 European lacertids. The eggs of all species increased linearly in both linear dimensions and mass during incubation. Across species initial egg mass was positively correlated with juvenile mass, with an allometric relationship exponent of 0.87. Initial egg mass across species increased proportionally with female mass to the power of 0.57. Moreover, an increase in maternal mass was also accompanied by an increase in clutch size. The number of eggs per clutch across species scaled with female mass to the power of 0.39. Removing the effect of female mass resulted in a negative correlation between egg mass and clutch size. Species for which the average egg size was lower than expected on the basis of female mass, tended to have larger relative clutch size. The total egg mass per clutch was about one third of female mass (exponent 0.94).

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Apathya is a lacertid genus occurring mainly in south-east Turkey and its adjacent regions (part of Iran and Iraq). So far two morphological species have been attributed to the genus, i.e. A. cappadocica (with five subspecies, A. c. cappadocica, A. c. muhtari, A. c. schmidtlerorum, A. c. urmiana and A. c. wolteri) and A. yassujica. The first of them occupies most of the genus’ distribution while A. yassujica is endemic of the Zagros Mountains. The topology and the genetic distances retrieved from this study, reveal that Apathya is a highly variable genus, which comes in agreement with the high morphological variation found in previous studies. Such levels of morphological differentiation and genetic divergence often exceed those between species of other Lacertini genera that are already treated as full species, justifying our view that the genus requires taxonomical revision. The phylogeographical scenario proposed reveals that dispersal and vicariant events in Anatolia and Southwest Asia throughout the Miocene, Pliocene, and Pleistocene resulted in the present distribution of the genus under study. Key geological event for the understanding of the phylogeography of the genus is the movement of the Arabian plate that led to the configuration of Middle East specifically the formation of the mountain ranges of Turkey and Iran.

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Apathya cappadocica is a medium-sized lizard species included in the family Lacertidae. The species is known from Türkiye, Northern Syria, Iraq, and Western Iran. Sexual dimorphism (SD), which is a phenomenon including phenotypic differences between males and females, has many effects on behaviour, shape and size characteristics. A total of 87 adult lizard specimens collected from south-eastern Anatolia were used in this study. The results of ANOVA showed that all morphometric features exhibited a pattern in which males have larger size than females. According to principal component analysis (PCA), the first three factors explain 81.553% of the total variance. Differences in head size between sexes have been well-documented in lizards and are associated with male-male aggression which results in mating success. This kind of pattern is supported by this study. Additionally, the results showed that males have more femoral pores, which is a signalling mechanism for sexual selection, than females. In conclusion, it can be accepted that the species in the genus Apathya has a similar pattern in accordance with the larger male theory.

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In this study, with habitat features, distribution, morphometric and meristic data relating to the 5 samples of subspecies Apathya cappadocica urmiana Lantz & Suchow, 1934, the new distribution model is presented in the west of Iranian plateau. These samples were collected during 2010-2013. Previously, the distribution range of this subspecies in the West Azarbaijan Province, was known from gorges on the west slope of the Urmia Lake. In this paper, this subspecies are also reported from province of Kurdistan, Kermanshah and Ilam, and therefore its distributional range is being extended to the south and west foothills of the Zagros Mountains and stop the distribution model in Ilam province to the south, the last limit distribution of this subspecies shown by topography and climate maps, and new information about the biology, distribution and morphology of this subspecies have been offers.

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The paper provides data on the current location of the type specimens of lacertid lizard’s taxa described by herpe- tologist Georgy F. Sukhov (1899–1942), as at July 1, 2020: Lacerta agilis tauridica Suchow, 1927 (lectotype [here designated] – ZISP No 12620, paralectotypes – ZISP No 3226, 3235, 3238, 3856, 10366в, 12230, 12231, 12520, 12619, 14110, NMNH No 2152 (14599–14600), 2163 (14621–14622), 2172 (14705–14712), 2184 (14772–14773), 2184 (14774–14777), 2188 (14872–14893), 2279 (15983–16037), 2279 (16038–16074), 2518 (16621)), Lacerta boemica Suchow, 1929 (lectotype [here designated] – ZISP No 30363, paralectotypes – ZISP No 16210, 30358- 30362, 30364-30398.1, NHM No 1960.1.4.26–30, 1965.337–342, NMNO no No), Apathya cappadocica urmiana Lantz et Suchow, 1934 (holotype – ZISP No 12657b, paratypes – ZISP No 11444, 12657a, c, 12658), Lacerta princeps kurdistanica Suchow, 1936 (holotype – ZISP No 11441.1, paratypes – ZISP No 11440, 11441.2–4, 11442, 11443). According to the International Code of Zoological Nomenclature (4th edition), the name Lacerta agilis caucasica Suchow, 1927 should be considered as a junior primary homonym of Lacerta caucasica Méhely, 1909, and the designation of the neotype of L. a. tauridica by Kalyabina-Hauf et al. must be rejected. The history of de- scription of taxa as well as a list of Sukhov’s publications (12 articles published in 1927–1948) are given. Localities, collector’s names and dates of capture of the type specimens are clarified. Anderson and Šmíd et al. indicated that Eiselt restricted the type locality of L. princeps kurdistanica; this is not true.

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A revisionary study of 366 specimens of Lacerta cappadodca WERNER, from Turkey, Iraq, and Iranhas revealed the existence of 5 subspecies: L. c. cappadodca WERNER (Kilikian Taurus to west of Malatya) ; L. c. wolteri (BIRD, 1936) (Amanus-Mountains to the Euphrates) ; L. c. muhtari ssp. nov. (east of Malatya and the Euphrates to the south of Lake Van, Turkey and to Sersang, Northeastern Iraq); L. c. schmidtlerorum ssp. nov. (around Diyarbakir and Viransehir); L. c. urmiana (LANTZ & STJCHOW, 1934) (South- eastern Turkey, Northeastern Iraq, Northwestern Iran).

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Western Iran in general and Ilam province in particular, has unique geographical and climatic conditions that support a rich flora and fauna. In view of the lack of in-depth studies of lizards of the region, an investigation was initiated in most areas of Ilam Province for an inventory of lizard species and their habitats. A total of 189 specimens were collected and identified from May 2005 to August 2009. Twenty one species belonging to 18 genera and 8 families were represented, including Agamidae: Laudakia nupta, Trapelus lessonae (formerly T. ruderatus), Trapelus ruderatus (formerly T. persicus); Eublepharidae: Eublepharis angramainyu; Gekkonidae: Bunopus tuberculatus, Cyrtopodion scabrum, Cyrtopodion heterocercum, Hemidactylus persicus, Stenodactylus affinis, Tropiocolotes helenae; Lacertidae: Acanthodactylus boskianus, Apathya cappadocica, Mesalina brevirostris, Ophisops elegans; Phyllodactylidae: Asaccus elisae; Scincidae: Ablepharus pannonicus, Eumeces schneiderii, Trachylepis aurata, Trachylepis vittata; Uromastycidae: Uromastyx loricatus; Varanidae: Varanus griseus griseus, Varanus griseus caspius. Comparing this list to the data provided by Anderson (1999), several lizards are reported for the first time in this region. With six species represented, gekkonids have the highest species diversity in the area.

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Climatic conditions changing over time and space shape the evolution of organisms at multiple levels, including temperate lizards in the family Lacertidae. Here we reconstruct a dated phylogenetic tree of 262 lacertid species based on a supermatrix relying on novel phylogenomic datasets and fossil calibrations. Diversification of lacertids was accompanied by an increasing disparity among occupied bioclimatic niches, especially in the last 10 Ma, during a period of progressive global cooling. Temperate species also underwent a genome- wide slowdown in molecular substitution rates compared to tropical and desert-adapted lacertids. Evaporative water loss and preferred temperature are correlated with bioclimatic parameters, indicating physiological adaptations to climate. Tropical, but also some popu- lations of cool-adapted species experience maximum temperatures close to their preferred temperatures. We hypothesize these species-specific physiological preferences may con- stitute a handicap to prevail under rapid global warming, and contribute to explaining local lizard extinctions in cool and humid climates.

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Altitudinal gradients are an important variable in testing the life history traits (e.g., longevity, age at maturity, and body size) of organisms. In this study, the life history traits of the Anatolian lizard Apathya cappadocica were examined from 3 populations from different altitudes (Kilis, 697 m; Sanliurfa, 891 m; Diyarbakir, 1058 m) from southeastern Anatolia, Turkey. Age structure was determined by using skeletochronology. Males in all populations were the larger sex; therefore, the populations showed male biases that were negative by the sexual size dimorphism index. Males in Diyarbakir (high altitude) were also younger than males in the other populations. There were no significant differences between the males and females of all 3 populations in terms of either age or snout–vent length except in the Sanliurfa population, in which males were larger than females. Life history traits of A. cappadocica across altitudinal gradients may be affected by climatic factors, as males from the middle altitude population in Sanliurfa, which inhabits a warmer and more arid environment, tended to be larger than males and females in Kilis and Diyarbakir.

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n this study the Check list lizards of Iraq were investigated. by reviewing the old and new data as well as carrying out field work and study of material in the Natural history Museum of Iraq as well as many departments and colleges in various universities, are discussed.Further, various relevant websites in the Internet specialized lizards. I found in this study 7 families, 27 genera and 50 species distribution in the different parts of Iraq. During this study I found Asaccus saffinae (Afrasiab & Mohamad, 2009) the first time in SheraSwar Cave in the Saffine Mountain near Erbil, Kurdistan and the first record new species in Iraq and found Ptyodactylus puiseuxi (Boutan, 1893) the first time in same area . Also found Carinatogecko heteropholis(Minton, S. Anderson, and J. A. Anderson, 1970) Which is one of the endemic species in western Iran in the Erbil western Zagros foothills in Erbil. Trapelus ruderatus (Olivier, 1804) found in the central of Iraq. Cyrtopodion scaber (Heyden, 1827) Previously found in southern Iraq But recently also recorded in the center and northern Iraq. Varanus nesterovi (Bohme, Ehrlich, Milto, Orlov & Scholz, 2015) new species in the northern of Iraq. Lacerta media (Lantz & Cyren, 1758) found newly in central and northern of Iraq and Timon kurdistanicus, Apathya cappadocica (Werner, 1902) (Suchow, 1936) northern of Iraq. I note the two families were finding Previously in Iraq and they did not record any new genus and species in Iraq.

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In recent years there has been an exponential increase in the amount of published DNA sequences, as it has become one of the most popular sources of data for reconstructing phylogenies. A number of studies have attempted to resolve the relationships of groups of lacertids using mitochondrial DNA sequence data, in particular Podarcis and Gallotia (e.g. THORPE et al., 1994; 1996; GONZALEZ et al., 1996; FU et al., 1997; HARRIS, 1997; HARRIS et al., 1998a; 1999; CASTILLA et al., 1999a,b). Reassessment of these data suggest some alternative phylogenies to those previously published, and also highlight possible problems. Two studies have attempted to unravel the phylogeny of the whole family using mitochondrial DNA sequences (FU, 1998; HARRIS et al., 1998b). By combining these essentially congruent data sets, and reanalysing levels of support for the phylogenies produced, a more complete estimate of relationships across the family is produced. This is then compared to alternative sources of evidence, primarily morphological (ARNOLD, 1989), biochemical (MAYER & BENYR, 1994) and karyological (OLMO et al., 1993). Reasons for discrepencies are discussed, as are the relative advantages and disadvantages of the different sources of phylogenetic inference.

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The evolutionary diversification of many terrestrial vertebrate groups is strongly linked to climatic events in the Cenozoic, the period from 65 Million years ago to today when modern animals first appeared. I investigated the effects of Cenozoic climate change on the taxonomic and morphological diversification of the Old World lizard family Lacertidae, with particular emphasis on the African radiation. African lacertids exhibit an unusual pattern of diversification, in which their highest species richness occurs in deserts north and south of the equator, despite being spread throughout the continent. This disparity is particularly surprising given that desert lacertids are thought to be evolutionarily younger than their mesic-dwelling relatives, suggesting increased diversification rates in arid habitats. To identify the evolutionary factors underlying this pattern, I use a combination of phylogenetic, morphological and ecological techniques. In Chapter 1, I apply Bayesian methods and fossil-based calibrations to molecular sequence data to construct a time-calibrated phylogeny for Lacertidae. I estimate that the family arose in the early Cenozoic, with the majority of their African radiation occurring in the Eocene and Oligocene. In Chapter 2, I describe changes in lacertid body shape across biomes and substrates, and find widespread morphological convergence in similar habitat types. I suggest that in addition to foraging demands, fluctuating and extreme climatic conditions, largely driven by precipitation and temperature, contribute to morphological convergence across independent arid-dwelling clades. Finally, I test if ancestral transitions in ecology, morphology, and rates of diversification temporally coincide with paleoclimatic events in the Cenozoic. I use High Resolution X-ray Computed Tomography to characterize changes in the skull related to life in arid habitats, and apply maximum likelihood methods to test if the origins of those traits temporally coincide with significant shifts in habitat, diversification rates and climatic changes. My results show that African lacertids experienced three major peaks in diversification, accompanied by the evolution of suites of arid-adapted morphological traits. These changes coincide with climatic shifts in Africa, including the transition from closed forests to open grasslands and savanna in the late Oligocene, prior to the peak temperatures of the mid-Miocene Climatic Optimum, and following the formation of the Benguela current leading to hyper-aridity in southern Africa. I conclude that deserts are important centers for reptile evolution, but that expected changes in climate due to global warming may outpace the ability of arid-dwelling species to adapt and persist in the future.

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Background: Although current molecular clock methods offer greater flexibility in modelling evolutionary events, calibration of the clock with dates from the fossil record is still problematic for many groups. Here we implement several new approaches in molecular dating to estimate the evolutionary ages of Lacertidae, an Old World family of lizards with a poor fossil record and uncertain phylogeny. Four different models of rate variation are tested in a new program for Bayesian phylogenetic analysis called TreeTime, based on a combination of mitochondrial and nuclear gene sequences. We incorporate paleontological uncertainty into divergence estimates by expressing multiple calibration dates as a range of probabilistic distributions. We also test the reliability of our proposed calibrations by exploring effects of individual priors on posterior estimates. Results: According to the most reliable model, as indicated by Bayes factor comparison, modern lacertids arose shortly after the K/T transition and entered Africa about 45 million years ago, with the majority of their African radiation occurring in the Eocene and Oligocene. Our findings indicate much earlier origins for these clades than previously reported, and we discuss our results in light of paleogeographic trends during the Cenozoic. Conclusion: This study represents the first attempt to estimate evolutionary ages of a specific group of reptiles exhibiting uncertain phylogenetic relationships, molecular rate variation and a poor fossil record. Our results emphasize the sensitivity of molecular divergence dates to fossil calibrations, and support the use of combined molecular data sets and multiple, well-spaced dates from the fossil record as minimum node constraints. The bioinformatics program used here, TreeTime, is publicly available, and we recommend its use for molecular dating of taxa faced with similar challenges.

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The aim of this study is to detect areas of endemism in lizards in Iran. This is the first study of its kind focusing on this subject. Areas of endemism for two families of lizards (Lacertidae and Gekkonidae) that have the highest number of endemic species than other lizard families in Iran were identified by Parsimony Analysis of Endemicity (PAE). Distribution data were collected from previous studies on the Iranian lizards and also from the recent literature on the descriptions of new endemic species. A total of 81 species of lizards were available for analysis. The study area was divided into a 2° × 2° grid of 63 Operational Geographic Units (OGUs). PAE was applied to the data matrix to detect areas of endemism and detected eight areas of endemism in southwestern Iran and near the Persian Gulf. Southern Iran is the main region where most species from Arabia came into Iran and were stopped in their dispersal. Two grids in southern and northeastern Iran were recognized as the areas with the highest density of species in the studied families. Lacertidae and Gekkonidae did not have a shared endemic species in the region (cells 59 and 60) but the area of endemism identified by PAE in the Persian Gulf region suggests that exchange between Iranian and Arabian herpetofauna was very high during interglacial periods. The distribution pattern of the endemic species of these families is concentrated in the region of the Alborz and the Zagros Mountains, but the single area of endemism in southern Iran has an important role in the historical biogeography of the Iranian herpetofauna. During interglacial periods, the Persian Gulf acted as a corridor between the herpetofauna of the two sides and this suggests the importance of this area of endemism for the Gekkonidae family. Also, the OGUs with the highest density of species are located around the country and, the lowest density is in the Central Plateau. PAE detected eight areas of endemism in southwestern Iran, but according to the number of species per units, two OGUs can be identified as high density in northeastern and southern Iran.

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The aim of this study was to predict suitable habitat for different clades of Apathya cappadocica in the Middle East. An additional goal was to calculate the ecological niche space of all lineages to determine the hypothesized degree of niche overlap and niche differentiation between these clades in Iran, Turkey, Iraq and Syria. All presence records of Apathya taxa in the study area were obtained and georeferenced from fieldwork, literature, and museums. All presence points were determined using 1 × 1 km grids covering the study countries. Environmental data such as bioclimate variables were also gathered at this resolution. Species distribution modeling was carried out using MaxEnt to determine current suitable regions for each lineage, and then the outputs were compared to find the degree of niche overlap between them. Our results found that all of the predicted models have high accuracy and some overlap with each other, especially for A. c. schmidtlerorum, but other lineages have distinctive models. Mean temperature of coldest quarter, isothermality, annual precipitation, and precipitation of coldest quarter were the highest contributed variables for A. c. cappadocica, A. c. wolteri, A. c. schmidtlerorum, A. c. urmiana, and A. c. muhtari, respectively. Ecological niche differentiation was found between all lineages, but A. c. schmidtlerorum shows niche similarity with other subspecies. Therefore, as previously recommended, A. c. schmidtlerorum can be synonymized with A. c. muhtari. Finally, our ecological results confirmed the specific status of all genetic lineages except for A. c. schmidtlerorum, consistent with the recommendation from a previous molecular study.

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Blood-serum proteins of the known subspecies of Apathya cappadocica (Werner, 1902) were studied comparatively by polyacrylamide disc gel electrophoresis. In order to obtain useful biochemical data for classification, differences between the electrophoreograms of the samples included in the morphologically different subspecies were distinguished qualitatively and quantitatively. These comparisons indicated that electrophoretic results supported morphological discrimination of the known subspecies of A. cappadocica.

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The life and work of the Alsatian Louis Amédée Lantz (1886-1953), a pioneer of European herpetology. A trained and professional research-chemist, the Alsatian Louis Amédée Lantz was an active and particularly dynamic herpetologist. His residence of nearly twelve years in Russia enabled him to make several field trips to regions such as the Caucasus and Iran. He always carried with him a home made telescopic net that he used to catch lizards. That net became symbolic of Lantz for most people around him. He realized significant herpetological collections mainly deposited in the Museum of the Zoology Institute of the Russian Academy of Sciences in St. Petersburg. Soon after the Russian Revolution in 1917, he had to leave the country and stayed for a few years in France before joining England. During this period, Lantz visited the French Pyrenees and the Mediterranean border (Hyeres Islands, Bandol), enabling him to discover for the first time oviparous populations of common lizard and also to describe a new species of lizard from the French Pyrenees. Lantz is also at the origin of the discovery of unisexual reproduction by parthenogenesis in reptiles. His collaboration with the Swedish amateur herpetologist Otto Cyrén, whom he met through the German herpetologist Willy Wolterstorff, was particularly successful throughout his career. Lantz died at the age of 66 years, in Switzerland, as he was about to join the team of herpetologists at the Natural History Museum in Paris.

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Little is known about altitudinal distribution of lizards in Iran. In the present study we studied distribution pattern of members of family Lacertidae along the eleveatinal gradient in Iran. To determine environmental drivers of distribution pattern of 48 lizard species, all known valid members of family Lacertidae, along elevational gradient in Iran. Firstly, we classified Iran digital elevation model (DEM) based on 100m intervals, that resulted in 56 altitudinal bands and number of species in each band was recorded. Secondly, we extracted mean value of following variables; altitude, slop, area, solar radiation index (SRI), normalized differences vegetation index (NDVI), annual precipitation, precipitation of wettest month, precipitation of driest month precipitation, precipitation of wettest quarter, precipitation of driest quarter, and precipitation of warmest quarter, and using VIF measure correlated variables were removed. Finally, we performed a multiple regression and found that area and precipitation of warmest quarter are the most important drivers of distribution pattern of family Lacertidae along elevational gradient in Iran. General distribution pattern of family Lacertidae was unimodal and maximum number of species living from 1475 m to 1675 m.

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Mountains play a key role in forming biodiversity by acting both as barriers to gene flow among populations and as corridors for the migration of populations adapted to the conditions prevailing at high elevations. The Anatolian and the Zagros Mountains are located in the Alpine-Himalayan belt. The formation of these mountains has influenced the distribution and isolation of the animal population since the late Cenozoic. Apathya is a genus of lacertid lizards distributed along these mountains with two species, i.e., Apathya cappadocica and Apathya yassujica. The taxonomy status of lineages within the genus is complicated. In this study, we tried to collect extensive samples from throughout the distribution range, especially within the Zagros Mountains. Also, we used five genetic markers, two mitochondrial (COI and Cyt b) and three nuclear (C-mos, NKTR, and MCIR), to resolve the phylogenetic relationships within the genus and explain several possible scenarios that shaped multiple genetic structures. The combination of results in the current study indicated eight well-support monophyletic lineages that separated to two main groups; group 1 including A. c. cappadocica, A. c. muhtari and A. c. wolteri, group 2 contains four regional clades Turkey, Urmia, Baneh and Ilam, and finally a single clade belonging to the species A. yassujica. In contrast to previous studies, Apathya cappadocica urmiana was divided into four clades and three clades were recognized within Iranian boundaries. The clades have dispersed from Anatolia to adjacent regions in the south of Anatolia and the western Zagros Mountains. According to the evidence generated in this study this clade is paraphyletic. Based on our assumption, orogeny activities and also climate fluctuations in Middle Miocene and Pleistocene have influenced to formation of lineages. In this study we revisit the taxonomy of the genus and demonstrate that the species diversity was substantially underestimated. Our findings suggest that each of the eight clades corresponding to subspecies and distinct geographic regions deserve to be promoted to species level.

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Apathya is a lacertid genus occurring mainly in south-east Turkey and its adjacent regions (part of Iran and Iraq). So far two morphological species have been attributed to the genus; A. cappadocica (with five subspecies, A. c.cappadocica, A. c.muhtari, A. c.schmidtlerorum, A. c. urmiana and A. c.wolteri) and A.yassujica. The first species occupies most of the genus’ distribution range, while A. yassujica is endemic of the Zagros Mountains. Here, we explored Apathya’s taxonomy and investigated the evolutionary history of the species by employing phylogenetic and phylogeographic approaches and using both mitochondrial (mtDNA) and nuclear markers. The phylogenetic relationships and the genetic distances retrieved, revealed that Apathya is a highly variable genus, which parallels its high morphological variation. Such levels of morphological and genetic differentiation often exceed those between species of other Lacertini genera that are already treated as full species, suggesting the necessity for a taxonomic revision of Apathya. The phylogeographical scenario emerging from the genetic data suggests that the present distribution of the genus was determined by a combination of dispersal and vicariance events between Anatolia and Southwest Asia dating back to the Miocene and continuing up to the Pleistocene. Key geological events for the understanding of the phylogeography of the genus are the movement of the Arabian plate that led to the configuration of Middle East (orogenesis of the mountain ranges of Turkey and Iran) and the formation of Anatolian Diagonal.

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In this study, a total of 29 specimens (16 , 10 and 3 juvenile) collected from Ihlara Valley were examined. The study was based on pholidosis, coloration and pattern, and body measurement as well as ecological and biologic observations. In conclusion it was determened that the population in the vicinity of Aksaray possess the same features as the nominate subspecies.

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Turkey is biogeographically diverse and consequently has a rich herpetofauna. As a result of active herpetological research, the number of species has steadily increased in recent years. I present here a new checklist of amphibian and reptile species distributed in Turkey, revising the nomenclature to reflect the latest taxonomic knowledge. In addition, information about the systematics of many species is also given. In total 35 (19.4%) amphibian and 145 (80.6%) reptile species comprise the Turkish herpetofauna. Among amphibians, 16 (45.7%) anurans and 19 urodelans (54.3%) are present. Among reptiles, 11 (7.6%) testudines, 71 (49%) saurians, 3 (2.1%) amphisbaenians and 60 (41.3%) ophidians are considered part of the herpetofauna. The endemism rate in Turkey is considered relatively high with a total of 34 species (12 amphibian species – 34.3% and 22 reptile species – 15.2%) endemic to Turkey, yielding a total herpetofaunal endemism of 18.9%. While 38 species have not been threat-assessed by the IUCN, 92 of the 180 Turkish herpetofaunal species are of Least Concern (LC), 13 are Near Threatened (NT), 10 are Vulnerable (VU), 14 are Endangered (EN), and 7 are Critically Endangered (CR). In addition, 6 species are in the DD (Data Deficient) category.

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Chemosystematic investigations on the position of Lacerta jayakari and the genera Gallotia and Psammodromus (Sauria; Lacertidae) 13 species of the genera Lacerta, Psammodromus and Gallotia (L. erhardii, L. filfolensis, L. bedriagae, L. cappadocica, L. jayakari, L. vivipara, L. trilineata, L. agilis, P. hispanicus, P. algirus, G. atlantica, G. galloti, G. stehlin:) have been examined by means of micro complement fixation tests (albumin) as well as by proteinelectrophoresis concerning 14 genetic loci. The results and their con-sequences are the follows: 1. L. cappadocica, L. bedriagae, and L. erhardii/L. filfolensis are representatives of phylogeneticly equivalent groups (subgenera). Their isolation in the Middle Miocene corresponds with the first contacts of the landmasses of Eurasia and Africa. 2. Lacerta jayakari may be considered as a representative of a further group equivalent in this aspect; though the immunological results would not exclude a position near the green lizards (subgenus Lacerta s. str.). 3. Because of this isolated position of L. jayakari for this species (and Lacerta cyanura) the subgenus Omanosaura subgen. nov. has been established. 4. Psammodromus hispanicus and P. algirus have probably been isolated of each other since the Middle Miocene, too. 5. The radiation of the genus Gallotia corresponds closely with genesis of the Canary Isles.

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Anhand der Ergebnisse einer Sammelreise des Natural History Museum of Crete (NHMC) im April 1999 werden neue Ergebnisse zur Herpetofauna Syriens vorgestellt. Wir sammelten an 30 Lokalitäten insgesamt 391 Exemplare in 43 Arten. Die Ergebnisse erweitern unser Wissen über die Verbreitung mehrerer Arten. Die systematische Stellung von vier Arten (Rana bedriagae, Ptyodactylus sp., Lacerta kultzeri, Mabuya aurata) wird im Lichte neuerer Revisionen der syrischen Herpetofauna diskutiert.

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Parts of the mitochondrial genes coding for 12SrRNA and 16SrRNA (together about 960 bp) were sequenced for all Mediterranean species of `Mountain lizards` of the genera Archaeolacerta (sensu lato) and Iberolacerta. All subspecies of the Iberian species Iberolacerta cyreni and I. monticola were included in this study. In addition, samples of Apathya cappadocica and Darevskia rudis were analysed to elucidate the relationships of the European `Mountain lizards` to their possible relatives in the Near East. Maximum parsimony and neighbour joining analyses lead to the following major conclusions: (i) the monophyly of the genus Iberolacerta is very well supported; (ii) Archaeolacerta bedriagae (the type species of the genus) is most basal with respect to the ingroup taxa. If we accept Iberolacerta as a genus, Archaeolacerta becames paraphyletic. Therefore, we propose to restrict Archaeolacerta to the type species and to treat A. mosorensis and A. oxycephala provisionally as members of the collective genus Lacerta; (iii) within the genus Iberolacerta three groups were found: a Pyrenean group, an Iberian group and I. horvathi. The relationships among these groups remain unresolved; and (iv) the Peña de Francia lizards, described originally as a subspecies of I. cyreni, are in fact more closely related to I. monticola.

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Investigated the albumins from 31 species and subspecies of the genus Lacerta s.1. by means of the immunoloical techniue Micro-Complement-fixation. Dendrograms were computed by means of the ktch-MargJiash algorithm. Moreover the taxa of the Lacerta saxicola and the Lacerta danfordi comlexes were analyzed by electrophoresis concerning 14 genetic loci. The results were discussel together with karyological and genitalmorphological data so far known yielding the following relationships: Lacerta graeca shows a closer relationshi to the subgenus Podarcis as does the quite closely related species air L. dugesii and L. perspicikata. Lacerta Iaevis probabl is connected closely to Podarcis, too. Lacerta parva shows a closer relationship to the `small izards` than to the sub-genus Lacerta s. str. A clear decision concerning the position of the Lacerta danfordi complex according to chemosystematical data was not possible. It is isolated from the other species probably about as long as L. puma. Biochemical differences between its `species` are too small to confirm their taxonomical revalorisation by Eiselt and Schmidtler Within the Lacerta saxicola complex the investigated taxa show a close relationship. Lacerta praticola and L. derjugini were definitly assigned to this group.

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Aim Body size is instrumental in influencing animal physiology, morphology, ecology and evolution, as well as extinction risk. I examine several hypotheses regarding the influence of body size on lizard evolution and extinction risk, assessing whether body size influences, or is influenced by, species richness, herbivory, island dwelling and extinction risk. Location World-wide. Methods I used literature data and measurements of museum and live specimens to estimate lizard body size distributions. Results I obtained body size data for 99% of the world`s lizard species. The body size–frequency distribution is highly modal and right skewed and similar distributions characterize most lizard families and lizard assemblages across biogeographical realms. There is a strong negative correlation between mean body size within families and species richness. Herbivorous lizards are larger than omnivorous and carnivorous ones, and aquatic lizards are larger than non-aquatic species. Diurnal activity is associated with small body size. Insular lizards tend towards both extremes of the size spectrum. Extinction risk increases with body size of species for which risk has been assessed. Main conclusions Small size seems to promote fast diversification of disparate body plans. The absence of mammalian predators allows insular lizards to attain larger body sizes by means of release from predation and allows them to evolve into the top predator niche. Island living also promotes a high frequency of herbivory, which is also associated with large size. Aquatic and nocturnal lizards probably evolve large size because of thermal constraints. The association between large size and high extinction risk, however, probably reflects a bias in the species in which risk has been studied.

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The etymology of the reptiles, especially the lizards of Iran has not been completely presented in other published works. Iran is a very active geographic area for any animals, and more especially for lizards, due to its wide range deserts and ecology. We have attempted to ascertain, as much as possible, the construction of the Latin binomials of all Iranian lizard species. We believe that a review of these names is instructive, not only in codifying many aspects of the biology of the lizards, but in presenting a historical overview of collectors and taxonomic work in Iran and Middle East region. We have listed all recorded lizards of Iran according to the order of the scientific names in the book of Anderson, The Lizards of Iran. All lizard species and types have been grouped under their proper Families, and then they have been alphabetically ordered based on their scientific binominal nomenclature. We also examined numerous published works in addition to those included in the original papers presenting each binomial.

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The global struggle to conserve as many species as possible with limited resources requires an improvement of our knowledge on the distribution of biodiversity. In Iran, the state of knowledge is poor for most groups of organisms, except few vertebrate groups and vascular plants. Reptiles are one of the best known, most diverse vertebrate groups in Iran, with a high rate of endemism (ca. 29%), but distribution patterns and related environmental drivers remain poorly understood. In the present study, based on a large publicly available dataset, we use general additive modelling (GAM) to identify explanatory variables for species richness of reptiles in Iran. Results indicate heterogeneity parameters (range +entropy) as the variables with the highest explanatory values. Based on the grid cells of the predicted environmental richness, using hotspot analysis, we suggest seven hotspots of reptile diversity (HRDs) across the country. Our results corroborate the previously recognized HRDs and detect three additional ones, located alongside the major mountain ranges around the central deserts plateau, particularly in the Zagros Mountains. Four of the largest HRDs (ca. 90%) situate within the Irano-Anatolian and Caucasus global biodiversity hotspot. In addition, our results reveal a large gap between identified HRDs and the current network of protected areas (PAs) in the country. While three of the detected HRDs in this study are partially touched (ca. 18%) by the PA network, overall, these areas are only covered by less than 10%. Therefore, the effectiveness of the current PAs for the protection of the reptile diversity of Iran is questionable.

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Lacertinae is one of the three lacertid lizard subfamilies with a geographical distribution confined to the Palaearctic. Several past attempts to reconstruct its phylogeny resulted in unresolved bush-like topologies. We address the question of whether the lack of resolution is due to insufficient data or whether this lack reflects a rapid succession of speciation events. We analyzed four partial and one complete gene sequences from mitochondrial and nuclear genomes, totalling roughly 3600 bp. We included 29 species representing all 19 genera suggested in recent revision of Lacertinae [Arnold, E.N., Arribas, O., Carranza, S., 2007. Systematics of the palaearctic and oriental lizard tribe Lacertini (Squamata: Lacertidae: Lacertinae), with descriptions of eight new genera. Zootaxa 1430, 1–86]. The resulting phylogeny, first, corroborates monophyly at the genus level for the suggested genera, as well as the finding that Atlantolacerta andreanskyi, until recently part of Lacertinae, belongs to the subfamily Eremiadinae. Second, we find that increasing the sequence length and combining multiple nuclear and mitochondrial sequences did not resolve the polytomy, suggesting that the inferred topology indicates a multiple cladogenesis within a short geological period, rather than a methodical artefact. Divergence time estimates, based on previous estimates of several node ages, range from 13.9 to 14.9 million years for the radiation event, however with very broad confidence interval. To associate the radiation with a narrower geological time we consider palaeogeographic and palaeoclimatic data, assuming that the Lacertinae probably evolved in Central Europe andWAsia after the collision of Africa and Eurasia. We suggest that this radiation may date to the late Langhian (ca. 14–13.5 million years) when geological events caused abrupt changes in regional water–land distribution and climate, offering a window of distinct conditions.

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Many animals display complex colour patterns that comprise several adjacent, often contrasting colour patches. Combining patches of complementary colours increases the overall conspicuousness of the complex pattern, enhancing signal detection. Therefore, selection for conspicuousness may act not only on the design of single colour patches, but also on their combination. Contrasting long- and short-wavelength colour patches are located on the ventral and lateral surfaces of many lacertid lizards. As the combination of long- and short-wavelength-based colours generates local chromatic contrast, we hypothesized that selection may favour the co-occurrence of lateral and ventral contrasting patches, resulting in complex colour patterns that maximize the overall conspicuousness of the signal. To test this hypothesis we performed a comparative phylogenetic study using a categorical colour classification based on spectral data and descriptive information on lacertid coloration collected from the literature. Our results demonstrate that conspicuous ventral (long wavelength-based) and lateral (short wavelength-based) colour patches co-occur throughout the lacertid phylogeny more often than expected by chance, especially in the subfamily Lacertini. These results suggest that selection promotes the evolution of the complex pattern rather than the acquisition of a single conspicuous colour patch, possibly due to the increased conspicuousness caused by the combination of colours with contrasting spectral properties.

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This report presents a new record of Iranolacerta brandtii brandtii from 30 km south of Tekab City, West Azarbaijan Province and 130 km south of the previously known distribution range of the subspecies; a new record of Iranolacerta zagrosica in Kaljonun mountain peak, Lorestan Province, about 70 km northwest of the type locality; a new record of Apathya cappadocica urmiana in the Manesht protected area in Ilam Province, which is the southernmost known locality of the subspecies; and a new record of Apathya yassujica in Pire Ghar, south of Farsan city in Chaharmahal va Bakhtiari Province, about 200 km northwest of the type locality.

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An updated checklist of the herpetofauna of Iran is presented based on records of amphibian and reptile species whose presence has been confirmed in Iran as a result of extensive field expeditions, examination of herpetological collections, literature review, and personal communications from researchers. The herpetofauna of Iran consists of 13 species and five subspecies of frogs and toads belonging to five genera and four families, eight species of salamanders belonging to four genera and two families, nine species and six subspecies of turtles, terrapins and tortoises belonging to nine genera and six families, one species of crocodile, one species of amphisbaenian, more than 125 species of lizards belonging to 36 genera and eight families as well as 79 species of snakes belonging to 37 genera and six families

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We present an annotated checklist for a total 241 reptiles and 22 amphibians including 5 frogs, 9 toads, 7 newts and salamanders, 1 crocodile, 1 worm lizard, 148 lizards, 79 snakes and 12 turtles and tortoises, includes the most scientific literature up to August 2014 and also based on several field surveys conducted in different Provinces of Iran from 2009 to 2014. We present an up-to-dated checklist of reptiles and amphibians in Iran. We provide a comprehensive listing of taxonomy, names, distribution and conservation status of all amphibians and reptiles of Iran. This checklist includes all recognized named taxa, English names for classes, orders, families, species, subspecies along with Persian names for species, including indication of native and introduced species. For the first time we report two non-native introduced reptiles from natural habitats of Iran. Of the total 22 species of amphibians in Iran, 6 (27.2%) are endemic and of the total 241 species of reptiles, 55 (22.8%) are endemic. Of the 22 amphibians species in Iran, 3 (13%) are Critically Endangered, 2 (9%) are Vulnerable and of the 241 reptile species 3 (1.2%) are Critically Endangered, 4 (1.6%) are Endangered and 10 (4.1%) are Vulnerable. Accordingly, this paper combines significant aspects of taxonomy, common names, conservation status and distribution of the Iranian herpetofauna.

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Ectothermic organisms, like terrestrial reptiles have very strong physiological tendency to maintain a stable internal environment with buffering the effects of outer conditions. However, they mostly tend to regulate their homeostasis in winter season via hibernation strategy. The members of family Lacertidae are hibernating reptiles, which have relatively rare winter activities. Although winter basking activity might serve a variety of biotic regulations in different species, the Anatolian lizards, Apathya cappadocica has not been documented for its winter activity so far. In this study, it is presented that the mating behavior of A. cappadocica in warming period in February 2019 from Siirt, Turkey. Any mating observation in this period has not been reported in literature in the Anatolian Peninsula up to date. The climatic oscillation with consequent extraordinarily warm days in winter might cause fluctuations in species phenology traits. However, this situation might also possess several risks in many aspects (i.e. early embryonic development, foraging, escaping from the predators) for the offsprings.

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In this study, it is aimed to determine the amphibians and reptiles species of Adana province. This study was conducted in September and October 2013 and February, March, May, April, and June 2014. As a results of the study, 4 anuran species belonging to three families, 2 urodelian species belonging to one family, 6 tortoise species belonging to five families, 16 lizards species belonging to 6 families, one worm lizard, 19 snakes species belonging to 4 families, with a total of 48 different species of amphibians and reptiles, showing distribution in Adana, were identified. However, the species of Neurergus strauchii, Pelobates syriacus, Anatololacerta pelasgiana, Darevskia valentini, Eirenis decemlineatus, E. eiselti, E. lineomaculatus, Rhynchocalamus melanocephalus, which were recorded in the literature previously, could not be found. With the field survey and literature records, 56 amphibian and reptile species belonging to 21 families were determined in Adana province. In addition, chorotype information of the species and distribution localities in Adana were given in detail.

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A study of the pholidosis in 4 series of Lacerta cappadocica from Amanus- und southern/northern Taurus-Mountains revealad a pattern of variation in seven scale counts that parallels climatic parameters. The mean values are higher in populations living in a warmoceanic rather than in a moderately warm continental climate. Corresponding results are known from Turkish Green lizards (SCHMIDTLER 1986). L. cappadocica (group wolteri-muhtari-schmidtlerorum) shows a clear relationship between the types of rock habitats and the colour pattern of the dorsum: populations in limestone areas are light-striped, whereas the populations in three investigated volcanic areas are light-spotted. The specimens in a transition area between the two geological formations show all intermediate stages between the striped and spotted phases.

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General morphology and size of erythrocytes of some lacertid lizards. Ophisops elegans, Lacerta cappodocica, Anatololacerta danfordi and Podarcis muralis, living in Turkey was studied using technique. The longest erythrocytes and nuclei were measured in O. elegans and the shortest ones in L cappodocica. The widest erythrocytes were recorded ill P. muralis and the narrowest ones in L. cappodocica, The widest nuclei were found in O. elegans mid the narrowest ones in L cappodocica.

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We present a comprehensive summary of the distribution of the lizards of Iran accompanied by an annotated checklist. The updated maps of distribution of all 146 species of 41 genera of 11 families are based on all available bibliographic records, catalogues of museum collections and our own field observations. The final dataset used for the distribution maps contains 8525 georeferenced records and cover 41% of the country when plotted on a grid of 0.25° × 0.25° resolution. The dataset is publicly accessible through GBIF portal (http://www.gbif.org/dataset/7db4f705-61ae-4c6e-9de2-06674e7d46b2). Following the latest biogeographic division of the country, ~53% of the species (76 species) inhabit the Iranian Province, ~41% (60 species) the Western Asian mountain transition zone, ~9% (13 species) the Turanian Province, and ~18% (27 species) the Arabian Province. In addition, ~2% (3 species) reach Iran from the Indo-Malay biogeographic region and ~2% (3 species) are believed to have been introduced to Iran by humans. Endemic species (46) represent ~32% of the known species diversity. The most species-rich family of lizards in Iran is Lacertidae with 47 species, followed by Gekkonidae (41), Agamidae (18), Scincidae (15), Phyllodactylidae (10), Sphaerodactylidae (4), Eublepharidae and Uromastycidae (3), Anguidae and Varanidae (2), and Trogonophidae with one representative.

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In this study, it was aimed to determine the amphibian and reptile species distributed in Kahramanmaraş province. Between the years 2016-2018, a total of 52 species (6 amphibians, 4 turtles, 21 lizards and 21 snakes species) belonging to 20 families were determined in Kahramanmaraş province during field surveys conducted at 451 localities. The records and their locations are presented in a map and a table. However, Bufo bufo (Linnaeus, 1758), Darevskia valentini (Boettger, 1892), Ablepharus chernovi Darevsky, 1953, Chamaeleo chamaeleon (Linnaeus, 1758), Parvilacerta parva (Boulenger, 1887), Anatololacerta pelasgiana (Mertens, 1959), Elaphe sauromates (Pallas, 1811) and Rhynchocalamus satunini (Nikolsky, 1899) were recorded for the first time from Kahramanmaraş.

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Knowledge on the spatial distribution of taxa is crucial for the decision-making processes in conservation and management of biodiversity that rely on precise distribution data. We present an annotated list for a total of 37 amphibian (20 caudatans and 17 anurans) and 141 reptile species (11 chelonians, 70 lizards, 3 amphisbaenians and 57 snakes) in Turkey, using both available scientific literature up to December 2020 and our own fieldwork data from 1987 to 2020. We provide a comprehensive listing of taxonomy, names, distribution and conservation status of Turkish amphibians and reptiles. The herpetofauna list will be particularly useful for establishing national conservation priorities as well as for placing Turkish fauna into phylogenetic and biogeographic contexts. We compiled information published in books, journals and various web sources and added our personal data. We projected the data in the WGS84 coordinate system and created an overlay grid with cells of 50x50 km2. The database comprises more than 500 grid cells and 11,913 records. As a result, the distribution of Turkish amphibians and reptiles has been extensively mapped with geographical information systems and a database has been created. The obtained data will be useful in planning future studies on taxonomy, ecology and conservation of Turkish amphibians and reptiles.

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In this research, it is intended to determine amphibian and reptile species distributed in Hatay province (East Mediterranean region, Turkey). For this aim, it is realized herpetological trip to al region of the province of Hatay in March, April, May, July, September and October in 2016 and in March and May in 2017. As a result of this study, it is recorded five anuran, two urodela species belong to five families, six chelonian belong to 5 families, and 17 lizard belong to seven families and 22 snake species belong to four families in the province Hatay (7 amphibians and 45 reptiles in total). As a result of this project; Trapelus lessonae (De filippi, 1865), and Eirenis barani Schmidtler, 1988 were recorded for in the province of Hatay in first. We report the most updated information regarding the herpetofauna of Hatay province.