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A variety of different methods are available for investigating the effects of past climate fluctuation on biota. Among them, molecular phylogeography and species distribution modeling approaches have been shown to be especially useful tools to trace past climate induced modifications of species’ geographic distributions. The results of both analytical approaches are here combined to better understand the influences of past climate changes on the fragmented distribution pattern of the lizard genus Iranolacerta that currently occurs in the northwest and central Zagros Mountains of Iran. While Iranolacerta zagrosica is restricted to few localities and cannot be modeled, the potential distribution of Iranolacerta brandtii suggested a large region of unfavorable habitat between northwest and the central Zagros Mountains populations. From the phylogenetic perspective, both species display deep genetic separation likely predating the Pleistocene. However, limited genetic diversity across this divided range of I. brandtii implies that the current separation is recent. Deeper genetic divergences were, nevertheless, uncovered within the northwest population. Since no recent geological events explain these results, the most likely explanation for such a distribution pattern is due to past climate fluctuations. Both sources of evidence suggest that during the early Holocene the northwest and Zagros populations of I. brandtii were connected, and the current pattern was shaped with their disconnection in the early Holocene. Further studies may identify potential glacial refugia for other species in this biodiverse region.

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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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Northwestern Iran has unique geographical and climatic conditions that support a rich flora and fauna. In view of the lack of in-depth studies on the lizards of the region, an investigation was started in the northern part of Ardabil Province for an inventory of this component of the fauna and their habitats. Collections were made from October 2003 to June 2005 and 165 specimens were collected and identified. Five families, 12 genera and 15 species are represented, including Agamidae: Laudakia caucasia, Phrynocephalus persicus, Trapelus ruderatus; Lacertidae: Lacerta media media, Lacerta strigata, Lacerta brandtii, Darevskia raddei raddei, Eremias strauchi strauchi, Eremias arguta, Ophisops elegans; Scincidae: Mabuya aurata transcaucasica, Eumeces schneiderii princeps, Abelepharus bivittatus; Anguidae: Pseudopus apodus and Gekkonidae: Cyrtopodion caspium caspium. Comparing this list to the data provided by Anderson (1999), it seems that most of the lizards are being reported for the Province for the first time. The families Gekkonidae and Anguidae are newly recorded, and the gecko Cyrtopodion caspium is first recorded from the west and northwest of Iran. With seven species represented in the area, lacertids have the highest species diversity among the lizard families and need further study. Habitat features also have been given for all species.

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TERRA TYPICA. Basminsk, between Tebriz and Teheran, northern Iran. DISTRIBUTION. The species is distributed in the north-western Iran, in the provinces Eastern Azerbaijan and Esfahan. On the territory of North Eurasia the only record is known in 1880 in the south-eastern Azerbaijan (Talysh). CONSERVATION STATUS. Uncertain due to poor knowledge on the species.

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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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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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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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Differences in surface structure (ober- hautchen) of body scales of lacertid lizards involve cell size, shape and surface profile, presence or absence of fine pitting, form of cell margins, and the occurrence of longitudinal ridges and pustular projections. Phylogenetic information indicates that the primitive pattern involved narrow strap-shaped cells, with low posteriorly overlapping edges and relatively smooth surfaces. Deviations from this condition produce a more sculptured surface and have developed many times, although subsequent overt reversals are uncommon. Like variations in scale shape, different patterns of dorsal body microornamentation appear to confer different and conflicting performance advantages. The primitive pattern may reduce friction during locomotion and also enhances dirt shedding, especially in ground-dwelling forms from moist habitats. However, this smooth microornamentation generates shine that may compromise cryptic coloration, especially when scales are large. Many derived features show correlation with such large scales and appear to suppress shine. They occur most frequently in forms from dry habitats or forms that climb in vegetation away from the ground, situations where dirt adhesion is less of a problem. Microornamentation differences involving other parts of the body and other squamate groups tend to corroborate this functional interpretation. Microornamentation features can develop on lineages in different orders and appear to act additively in reducing shine. In some cases different combinations may be optimal solutions in particular environments, but lineage effects, such as limited reversibility and different developmental proclivities, may also be important in their genesis. The fine pits often found on cell surfaces are unconnected with shine reduction, as they are smaller than the wavelengths of most visible light.

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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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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 distribution of Iranolacerta brandtii previously was limited to the Iran. Anew locality is reported here in eastern Turkey. Data based on meristic pholidosis characters, metric measurements and color-patter features of the specimens from eastern Turkey were given in detail and compared with data given in the previous literature. In addition, the first record of Iranolacerta brandtii from outside of Iran is reported here.

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Population of Iranolacerta brandtii lizard including 56 (21 females, 34 males, 1 juvenile) samples were examined for helminths. 17 of them were found to harbour one or more helminth parasites, while 39 didn’t harbor any. Two helminth species were determined. These belong to Phylum: Nematoda, Spauligodon aloisei Casanova, Milazzo, Ribas & Cagnin, 2003 and Skrjabinodon medinae. García-Calvente, 1948. This study represents new host and locality records in both host lizard and the helminth species. Sp. aloisei is recorded for the first time; Sk. medinae is the third report from Turkey nevertheless Sk. medinae is a new host record for I. brandtii.

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Since the work of PETERS (1962) Lacerta brandtii DE FILIPPI, 1863 was regarded as the closest rela- tive of the L. parva I L. fraasii group within the collective genus Lacerta (e. g. ARNOLD 1989; BISCHOFF 1991). The crown-shaped microornamentation on the hemipenial epidermis of L. brandtii seems to exclude this hypothesis and does, however, not offer an alternative resolution, due to its obvious multiple origin. Candi- dates of close relationship to L. brandtii are the Rock Lizards or the L. laevis / L. danfordi group. Other methodological approaches are required to resolve this question.

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In April 1995, during unseasonably cold, wet weather. tive specimens of Lacerta lmmdtii were caught in Iran: one 35 km east of Tabriz next to the small lake at Guritshul (1900 m), and four near Bazoft in Kuh Rang (2500 m). 150 km west of Esfahan. The latter is only the second report for this mountain range since the Street Expedition of 1968 collected seven specimens. No differences in pholidosis were found between the four male Kuh Rang lizards and the published data for the populations in north-western Iran. It appears that yellow is less prominent in the coloration of the L. lmmdtii of Kuh Rang. The annual change in coloration is described. Around three weeks after ending hibernation the male`s dorsal and lateral regions of the frontal part of the body change from dull brown into bright green, the posterior half into a fair hazel. Throats can still be yellow at this stage but will frequently change into blue, the colour often also sprea- ding to the labials. From faintly yellow the belly will turn brightly (greenish) yellow. the region around the cloaca, the underside of the tail and the undersides of the hind legs change into orange. Unlike some literature suggests, this colour is not found in the pelvic region of the supposedly related species Lfraasii and L parva. Around July the dorsal and lateral co- lours darken, the green disappears, and the ventral colours pale. Even before hibernation starts some throats may already acquire a blue tinge. The animals lived on the ground, moving be- tween the scarce vegetation and some larger boulders. When collected, they had apparently recently ended their hibernation, these were just males which had not shed their skin, they were dull looking due to the dried clay. Faecal pellets of animals from both localities mainly contained many small-sized Coleoptera. At both localities the soil consisted of clay with sunken pieces of limestone. Ophisops cf. ele- gans and Bufo viridis were found to be sympa- tric. A list with chance finds of other reptiles and amphibians is also provided.

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The Arasbaran Protected Area is a forested and mountainous area, which is located in northern part of East Azerbaijan province and bordered to the north by Armenia and Azerbaijan and southern Aras River of the Iranian Plateau confined to 38°40` to 39°08`N and 46°39` to 47°02`E. A study on the status of Sauria in this area was carried out from June to September 2011 and 2013. A total of 141 specimens were collected and identified, which represented four families, 11genera, and 12 species and subspecies, including collected Agamidae: Paralaudakia caucasia, Phrynocephalus persicus, Trapelus lessonae, Anguidae: Pseudopus apodus, Lacertidae: Darevskia raddeii, Iranolacerta brandtii, Eremias strauchi, Lacerta media, Lacerta strigata, Ophisops elegans and Scincidae: Eumeces schneideri Ablepharus bivittatus. The Lacertidae with six species, showed the highest diversity among the families represented here. In this study a new locality was found for Lacerta strigata 30 km north of kalibar, in the Arasbaran.

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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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Squamata or scaled Reptiles are the largest order of new Reptiles including Lizards, Snakes and Amphisbaenia. They have formed 95 precent of new Reptiles. Our goal is Lizard Biodiversity of Torbat-e Heydaryeh in Razavi Khorasan Province. The study of Lizards Biodiversity of Torbat-e Heydaryeh in Razavi Khorasan Province was carried out in 2012 until 2013. In this research 132 specimens were collected and observed and identified on the basis of morphological, morphometric and meristic characters. The collected and observated Lizards belonging to 5 families: Agamidae, Lacertidae, Scincidae, Gekkonidae and Varanidae including 8 genera and 12 species. Results showed that Agamidae and Lacertidae families have the most frequency. The Agamidae family has the most genera and Lacertidae family has the most species. laudakia caucasia, laudakia microlepis, Trapelus sanguinolentus and Mesalina watsonana were the dominant species in this region and had a wider distribution rang in coparision with other species.

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Die Arbeit präsentiert skelettochronologische Daten zur Altersstruktur und zum Wachstum von Iranolacerta brandtii (DE FILIPPI, 1863) einer ostanatolischen Gebirgspopulation (2363 m ü.M.) aus dem Gebiet des Dorfes Karadula im Bezirk Çaldıran, Provinz Van (Türkei). Das Alter der dreiundzwanzig (19 Männchen, vier Weibchen) untersuchten Exemplare lag bei Männchen zwischen drei und sechs, bei Weibchen zwischen vier und fünf Jahren, wobei sich anhand der Stichprobe kein statistisch signifikanter Unterschied nachweisen ließ. Die Geschlechtsreife wurde von Männchen wie Weibchen im zweiten oder dritten Jahr erreicht. Die mittlere Kopf-Rumpf-Länge der Weibchen (64.27 ± 1.42 mm) übertraf die der Männchen (58.41 ± 1.17 mm) signifikant (p = 0,029).

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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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DNA sequences from parts of the 12S, 16S and cytochrome b mitochondrial genes, which totalled 1049 aligned base pairs, were used to estimate the relationships of 49 species of Lacertidae, including representatives of 19 out of the 23 recognized genera and 23 species of the paraphyletic genus Lacerta. These data were used, together with morphological information, to estimate the relationships within the family. Molecular evidence corroborates the monophyletic status of many genera and species groups originally based on morphology. It indicates that Psammodromus forms a clade with Gallotia, which is the sister taxon of all other lacertids. These comprise three units: the primarily Afrotropical armatured group; the largely Oriental Takydromus; and the west Palaearctic Lacerta and its derivatives, Podarcis and Algyroides. Morphology also supports the first three assemblages, but suggests that they are derived from a paraphyletic Lacerta. Within Lacerta and its allies, DNA sequence analysis corroborates the affinity of some members of each of the subgenera Lacerta s. str. and Timon, and of the L. saxicola group. It also supports the relationship of L. monticola, L. bonnali and L. horvathi, and suggests that the L. parva–L. fraasi clade and L. brandti are not related to Psammodromus–Gallotia, as morphology indicates, but instead are associated respectively with the L. danfordi and L. saxicola groups. DNA sequence data provide additional evidence that the eastern Arabian `Lacerta` jayakari and `L.` cyanura are members of the armatured clade and also sister species. Our analysis supports an origin for present lacertids in west Eurasia. The armatured clade invaded Africa, probably in the mid-Miocene, spreading widely and evolving increasingly xeric-adapted forms, one lineage of which later moved back into the Palaearctic. `Lacerta` jayakari and `L.` cyanura are assigned to Omanosaura, Lutz and Mayer 1986. The name Gallotiinae Cano, Baez, Lopez-Jurado and Ortega, 1984 is available for the Gallotia–Psammodromus clade, Eremiainae Shcherbak 1975 for the armatured clade and Lacertinae for Lacerta, Podarcis and Algyroides. Two new subgenera of Lacerta are proposed here: Caucasilacerta for L. saxicola and its allies, and Parvilacerta for L. parva and L. fraasi.

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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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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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During recent herpetological field work (june 2012) a new locality was found for Iranolacerta brandtii brandtii (DE FILIPPI, 1863) 40 km north of Varzeghan, in the East Azerbaijan province of Iran. Two specimens were collected and deposited in the Madani University Zoological Collection under numbers A49 and A50. A description is given on the local habitat, as well as 20 metric and meristic characters of the two specimens.

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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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Several recent papers have reviewed the life and work of French herpetologist Louis Amédée Lantz. They have detailed the composition of his collections deposited in several museums. However, since then, several other important specimens from his collections deposited at the Natural History Museum (NHM, UK) have come to light and we here present all of them in detail. We discovered paralectotypes of Lacerta saxicola obscura Lantz & Cyrén (BMNH 1918.11.21.5–7), syntypes of Lacerta boemica Sukhov (BMNH 1960.1.4.26–30, BMNH 1965.337–342) and Lacerta viridis media Lantz & Cyrén (BMNH 1960.1.4.25, 1966.512). We also identified numerous specimens from the French Mediterranean islands in Lantz’s collection deposited at the NHM, some of which represent the first reported specimens of their species from certain islands. We here provide data on all these specimens. We also place the Mediterranean island specimens from the Lantz collection in their historical context and emphasize the historical and taxonomic value of these collections.

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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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Materials and methods. Observations of Amphibians and Reptiles were carried out during two tourist trips in March 2016 and in May 2018 in the Iranian provinces of Gilan and Ardebil.
Results. New data on the distribution of 6 species of Amphibians (Bufo eichwaldi, Bufotes variabilis, Hyla orientalis, H. savignyi, Pelophylax ridibundus, Rana pseudodalmatina) and 21 species of Reptiles (Emys orbicularis, Paralaudakia caucasia, Trapelus ruderatus, Darevskia chlorogaster, D. defilippii, D. raddei, Eremias strauchi, Iranolacerta brandtii, Lacerta strigata, Ophisops elegans, Ablepharus bivittatus, Heremites auratus, Pseudopus apodus, Eryx jaculus, Eirenis punctatolineatus, Hemorrhois ravergieri, Platyceps najadum, Telescopus fallax, Xerotyphlops vermicularis, Natrix natrix, N. tessellata) in the study area were obtained. The author compares the obtained data with the results of other Herpetological researches in the region.
Conclusions. In general, the herpetofauna of the Caspian slopes of the Talysh Range in Iran is an inseparable part of mesophilic herpetocomplexes with the prevalence of gyrcan elements common from the north-western foothills of Talysh in Azerbaijan to the Western Kopetdag in Turkmenistan.

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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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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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During our long-term fieldwork on the Iranian plateau in 2000 and 2002, we collected and examined a series of lacertid lizards, belonging to the genus Lacerta from various parts of the Zagros Mountains of western and southwestern Iran, from a morphological point of view. Based on the collected material, two new taxa are described: Lacerta yassujica sp.n. and Lacerta brandtii esfahanica ssp.n. Based on all the available evidence, L. yassujica is closely related to Lacerta (Apathya) cappadocica. A short account on taxonomy and biogeography of the studied taxa is given.

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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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The authors report on a herpetological excursion from April 22 to May 7 to northwestern Iran. The route led from Tehran via Esfahan, Chelgerd, Kuhdasht, Kermanshah, Marivan, Täbriz, Zanjan and Manjil back to Tehran. The first part of the article deals with reptiles and amphibians found in the Zagros Mountains.

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In the first part of our travel report, we presented our reptile and amphibian finds in the Zagros Mountains. In the second part we report on our observations in the mountains of Tabriz, Zanjan, Manjil and Teheran between May 3rd and 7th, 2016.

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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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The Persian Lizard, Iranolacerta brandtii, was until recently considered to be restricted to north-western Iran (Azerbaijan and Esfahan provinces). However, two recent studies have revealed the existence of populations in Eastern Anatolia, extending the range of this species for about 230 km westwards. The fragmented distribution of this species has been considered to be a consequence of the climatic oscillations during the Pleistocene and Holocene, which created events of alternating contact and isolation of populations in distinct glacial refugia. According to our obtained genealogy derived from three mitochondrial fragments (12S rRNA, 16S rRNA and cytb), the Turkish specimens cluster together but form an independent clade, sister to the individuals from Tabriz in Iran. The separation of these two clades is concurrent with the cladogenesis between the Esfahan and Ardabil clades, estimated to have taken place during the late Holocene.

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According to recent revision of Lacertidae family by Arnold et al. (2007), two species of Iranolacerta genus are found in Iran: Iranolacerta brandtii and Iranolacerta zagrosica. Both species have limited range of distribution and unknown biological and ecological status. Therefore, in this study a total of 25 Iranolacerta brandtii specimens (10 males, 13 females, and 2 juveniles) were collected from northwest of Iran. First, based on the morphological features including coloration pattern, morphometric measurements and pholidosis characters the species was studied. Then, habitat features and new distribution localities were documented. For the first time, some reproductive aspects, such as clutch size, follicles number, testis length and color are reported. Feeding ecology of this species was investigated through analysis of stomach contents.

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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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This book shows a comprehensive picture of the reptiles, excluding snakes, living in Europe, North Africa, Middle and Near East and Central Asia. The bulk of the book is an annotated checklist and a distributional atlas of approx 500 species of lizards, crocodiles, turtles and terrapins, and amphisbaenians, living in the Western Palearctic. Information on distribution, subspecies, chorotype and main references are provided for each species, as well as 226 colour maps showing the global distribution of the species on a grid of one degree. For each species map the bibliographic and original sources (more than 850 sources are listed) are indicated. A further 83 maps show the distribution of all genera and main species groups of Palearctic reptiles. Beside the checklist and the atlas, in some additional chapters the following arguments are treated: Materials and methods; status of knowledge on the Palearctic fauna; composition of the Western Palearctic reptile fauna (including a statement on biodiversity and species richness); descriptive biogeography (including a discussion on the Palearctic region boundaries based on reptile distribution and the herpeto-geographic sectors of the Western Palearctic); conservation status. A list of more than 730 references quoted in the text and high quality colour plates including photos of the most of the supraspecific taxa living in the study area completes the book.

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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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This study explores the relationships between recent Iranian lizard species distributions and the observed climate, as well as potential future distributions of species. For this purpose, an ensemble of seven algorithms was used to forecast the distributions of 30 species for the recent and future (2070) based on the averages of 14 global climate models under optimistic (RCP2.6) and pessimistic (RCP8.5) scenarios. Annual precipitation (n= 16) and annual mean temperature (n= 7) were identifed as the most important variables in determining the distribution of 76.66% (23 out of 30) of the species. The consensus model predicts that the ranges of 83.33% of species (n= 25) have the potential to expand poleward at higher latitudes while preserving the majority of their recent distributions (except for four species). Furthermore, the ranges of the remaining species (n= 5) will be preserved at higher latitudes. However, they (n= 22) may contract slightly (n= 13) or excessively (n= 9) in the south of their distribution range at lower latitudes. These results indicate that species (N= 19) situated in mountainous areas such as the Zagros, Alborz, and Kopet Dagh may move or maintain their range at higher elevations as a result of future climate change. Finally, this study suggests that 30% of species (n= 9) may be threatened by future climate change and that they should be prioritized in conservation eforts.

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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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This is the first report of the occurrence of Iranolacerta brandtii in Eastern Anatolia. The distribution of I. brandtii is extended approximately 230 km eastwards into Van province, Turkey, showing that this species is not endemic to Iran as previously stated in the literature. Seven specimens were collected from four different localities between May and September 2014. Specimens were evaluated with respect to their morphological characters and some ecological features and their taxonomical status is also discussed.