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Timon, a small genus of lacertid lizards, includes four species distributed in two separate ranges in the western and eastern part of the Mediterranean Basin. Phylogenetic relationships between the two groups have not been resolved, and the taxonomic situation of the two subspecies of the eastern representative of the genus, Timon princeps, is not clear. To address these questions, partial DNA sequences of two nuclear (β-fibrinogen intron 7 and C-mos) and three mitochondrial (cytochrome b, 12S rRNA and 16S rRNA) genes were analyzed. Based on the high genetic distance between the two subspecies of T. princeps we promote their taxonomic status to full species, Timon princeps and Timon kurdistanicus. Divergence time estimates based on other lacertid species suggest that the separation of the green (Lacerta) and ocellated (Timon) lizards took place around 12 My ago, and that the Eastern group underwent speciation around 4-5 my ago, perhaps associated with the uplifting of the Zagros mountains. As expected given this ancient divergence and complex paleogeography, considerable levels of genetic diversity are recovered within both taxa, with geographically close individuals showing very divergent haplotypes.

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Aim The ocellated lizards of the genus Timon, comprising six species that are distributed across continental Asia, Europe and Africa, offer an interesting model to study the evolution of ecological niches through comparative phyloclimatic analysis. Our study provides insights into the evolutionary history of the ocellated lizards and helps to understand the role of climatic niche evolution during the speciation process. Location Eastern and western margins of the Mediterranean basin. Methods A dated molecular phylogeny was estimated based on three mitochondrial and two nuclear genes. Using multivariate statistics, species distribution models were developed to characterize the Grinnellian niches of all species. Subsequently, ancestral environmental niche occupancy of each taxon was reconstructed using niche occupancy profiles. Niche divergence among species was quantified by computing multivariate niche overlaps via twodimensional and n-dimensional approaches. Results Phylogenetic analysis supports that the ancestor of Timon diverged into the eastern and western groups following multiple vicariance events that shaped the current distribution pattern of Palaearctic lizards. High complexity in the ecological niche evolution between the Mediterranean and non-Mediterranean climatic regions was detected. The generally low niche divergence among members of the eastern group and the remarkable climatic divergence within the western group highlight an important role of temperature seasonality in a Mediterranean and Atlantic climate context. The results also suggest niche conservatism in terms of microhabitats described by vegetation cover. Main conclusions The ocellated lizards provide an interesting example of a vertebrate radiation where niche shift (with or without vicariance) and niche conservatism alternate in different niche axes shaping current biogeographical patterns.

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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 genus Timon currently comprises six species and is distributed in Europe, Asia and North Africa. The two European species are Timon nevadensis in south-eastern Spain and Timon lepidus in the rest of the Iberian Peninsula and parts of southern France (as well as an adjacent small area in Italy). There seems to be some intergrading between those two species. Two subspecies are recognized beside the nominate form Timon lepidus lepidus: Timon lepidus ibericus in north-eastern Iberia and Timon lepidus oteroi on Illa de Sálvora. Molecular research showed recently that five different lineages can be distinguished in Timon lepidus (MIRALDO et al. 2011). The various lineages differ to some extent in colour and pattern. Recently, PEEK (2011, 2017) reported a small-bodied form of T. lepidus from the north side of the Sierra de Gredos. Moreover there are two North African species of this genus, Timon pater and Timon tangitanus. Timon princeps and T. kurdistanicus inhabit regions in Asia, the former is found in Iran and the latter in Turkey, Iran and Iraq.

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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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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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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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New informations concerning systematical questions within the family Lacertidae, which were published during the last year, are presented.

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Ein Bericht über die Neuaufsammlung der „farsischen Zagroseidechse`, Lacerta princeps princeps BLANFOBD 1874, von der während der nahezu 100 Jahre, die seit ihrer Erstbeschreibung verstrichen sind, erst 4 Exemplare bekannt geworden waren. Ihre Lebendfärbung und ihre Jugendtracht werden erstmalig beschrieben und ebenso wie ihre Beschuppung und ihr Schädelbau, mit der durchaus eigenständigen „kurdischen Zagroseidechse`, Lacerta princeps kurdistanica SUCHOV 1936 verglichen.

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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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Lacerta princeps subsp. princeps is endemic to Iran and found from the new locality of north slops of Dena mountain near Cisakhat in this study. Mitotic chromosome studies on bone marrow cells of male and female revealed 2n=35 and 2n=36 chromosomes respectively. The karyotype consists of 34 autosome chromosomes including: one pair of biarmed metacentric macrochromosome, 15 pairs of uniarmed chromosomes and one pair of microchromosome. in addition, it seems that male has 1 uniarmed X chromosome and female has 2 uniarmed XY chromosomes, which Y chromosome was smaller than X. The presence of 1 pair biarmed metacentric macrochromosome in L. perinceps princeps separates this species from another species that examined from karyologically point of view. It seems that this pair chromosome originate from the fusion of 2 telocentric chromosomes. Chromosome count for this subspecies is reported here for the first time.

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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 new data on distribution of Timon princes (Blanford) in Southeastern Anatalia were obtained. All reliable data on its distribution in Turkey, including new locality, are presented on the map. The meristic pholidolial, metric (morphometric) characters and color-pattern features of specimens of T. princeps collected from 19 km SE of Siirt, Southeastern Anatolia, Turkey were given in detail and compared with the specimens from Iran, Iraq and other Turkish localities with regard to literature. In addition, Turkish and Iran populations of T. princes were compared statistically with each other in terms of meristic pholidolial characteristics and metric measurements.

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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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Aims The Zagros Mountains are a part of the 20th global hotspot, the Irano-Anatolian biodiversity hotspot. In this study, we aim to develop a comprehensive checklist of endemic herpetofauna species in the Zagros Mountains as one of the biodiversity hotspot regions, to provide more information about this important area and the necessity of conservation programs to protect it. Materials & Methods The Zagros Mountains, with an area of about 533,543km2, ranges from Turkey and Iraq to western and southwestern Iran along the eastern edge of the Persian Gulf. A list of endemic species has been collected from the literature review. Findings This region contains 3 species and 7 subspecies of endemic amphibians belonging to three genera and two families, the Salamandridae (8) and the Bufonidae (2). Neurergus and Calliopersa are endemic to this hotspot. There are 40 species and 6 subspecies of endemic reptiles belonging to 24 genera and 10 families. The families with the greatest number of endemic species are the Gekkonidae, Phyllodactylidae, and Colubridae. Three genera, Asaccus, Mediodactylus, and Eirenis, dominate the region, with 32 endemic taxa. There are also two endemic genera, Parsigecko and Lakigecko. Conclusion Many amphibians in the Zagros Mountains, especially all the species of the genus Neurergus, are categorized in IUCN (the International Union for Conservation of Nature) Red List and CITES (the Convention on International Trade in Endangered Species of Wild Fauna and Flora). The habitats of the Zagros Mountains herpetofauna, especially those of endangered and endemic species, should be protected and managed to maintain or restore populations of the declining species.

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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 western parts of Iran were visited twice. Beside many other interesting species both subspecies of the Zagros lizard were also found. The observations, the biotope and some of the behaviour of these animals are dealt with.

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The present work reports on Lacerta viridia atrigata Eichwald and L. princeps Blanf., from Iraq along with detailed notes on their natural . history, coloration as well as their taxonomy. Characters ot taxonomic importance are pointed out and a key to the available species of the Iraqi Lacerta is provided. Important evoiut!onary tendencies of certain taxonomic features are pointed out with some evolutionary notes related to the subject. The publlcation of Hass and Werner (1969) is critically discussed in relation to the present work.

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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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The schism between North Africa and Southern Europe caused by the opening of the Strait of Gibraltar and the consequent refilling of the Mediterranean basin at the end of Messinian salinity crisis (MSC), 5.33 million years ago, has been advocated as the main event shaping biogeographical patterns in the western Mediterranean as exemplified by the distribution of species and subspecies and genetic variation within the ocellated lizard group. To reassess the role of the MSC, partial sequences of three mitochondrial DNA genes (cytochrome b, 12S and 16S ribosomal RNA) and two nuclear genes (β-fibrinogen and C-mos) from species of the ocellated lizard group were analysed. Three alternative hypotheses were tested: that divergence was initiated (i) by post-MSC vicariance as the basin filled, (ii) when separate populations established either side of the strait by pre-MSC overseas dispersal, and (iii) by post-MSC overseas dispersal. The pattern and level of divergence detected clearly refute the post-MSC vicariance hypothesis, and support a model of divergence initiated by earlier overseas dispersal. Indeed, our best estimate is that the basal Euro-African divergence predates the MSC event by several million years. The estimated divergence times among the populations in former Miocene Mediterranean islands, the current Betic and Rifian mountains, from adjacent mainland populations suggest overseas dispersal for the former and overland dispersal, or perhaps vicariance, for the latter. These results suggest that the MSC may have played a much less important role in shaping the current western Mediterranean biogeographical patterns than might have been anticipated from the dramatic nature of the episode.

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This report describes the discovery and detailed description of a new small sized morph of ocellated lizard from the northern slopes of the Sierra de Gredos (Castilla y Leon, Spain). Morphological and molecular analysis showed that this new morph is different from the common species of ocellated lizard (Timon lepidus) on the Iberian peninsula in body size, sexual size dimorphism and cytochrome b haplotype. DNA sequencing revealed a unique and highly divergent cytochrome b haplotype indicating a long-term separation from other species of ocellated lizards. Evolutionary mechanisms that may have contributed to the formation of the small sized morph are discussed. The results presented in this paper suggest that this new morph is likely to be recognized as a full species in the near future.

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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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The Arsanjan county has various habitat types (grasslands, mountains, rocky and shrubbery areas) that is located northeast of Fars Province, Iran. The herpetofauna of Arsanjan county is unclear and there is no biosystematic study so far. The aim of the present study is to investigate the lizard’s fauna of Arsanjan. The study area is located between the coordinates as follow: 29°38` _ 30°00` N and 53°07` _ 53°43` E. All the specimens were collected in different regions of Arsanjan county during this survey from 2018 to 2020. Specimens were identified according to the valuable resources. The collected specimens represented ten species, nine genera and four families including: Large scaled rock agama (Laudakia nupta), Brilliant ground agama (Trapelus agilis) and Horny scaled agama (Trapelus ruderatus) (Agamidae); Keeled rock gecko (Cytopodion scabrum) (Gekkonidae); Snake-eyed Lizard (Ophisops elegans), Persian long tailed lizard (Mesalina watsonana), Persian racerunner (Eremias persica) and Zagrosian lizard (Timon princeps) (Lacertidae); Schneider Skink (Eumeces schneiderii) and southern grass skink (Heremites septemtaeniatus) (Scincidae). Among the identified species Timon princeps is a new record from the area.

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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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Field observations show the Zagrosian lizard Lacerta princeps kurdistanica in SE Turkey (Mardin hills) as an inhabitant of the shrubby oak forests covering the slopes of the valleys. Within these forests the lizard prefers the oak-shrubs. Other reptiles which may be food competitors of L. princeps are living in different habitats. For example, Agama stellio is found on or between rocks, while Lacerta trili- neata media lives only in relativly moist regions near water. Population density of L. princeps appears to be low in the Mardin hills. Colour and flight-behaviour of L. princeps seems to be an antipredator adaption against the short- toed eagle Circaetus gallicus which was often seen in that region. 6 d` and 1 S? of L. princeps kurdistanica were caught and are now living in terraria. The males are aggressive, so that they are kept in different cages, some of them together with other Lacerta species. No aggression was seen against a male of L. v . viridis or from this animal against the L. princeps male. In the expressive behaviour of L. princeps males we found a `nodding` very similar to that seen in males of Canarian lizards. No behavioural character is corresponding exclusively with the behaviour of the Lacerta s. str. group (L. viridis, L. agilis, L. schrei- beri, L. trilineata, L. strigata). There is no reason to extend the weil defined Lacerta s. str. group by adding the Zagrosian lizard. A group consisting of the Canarian lizards, Lacerta lepida, Lacerta princeps, and Lacerta jayakari is based on plesiomorphic characters and thus it is not a monophyletic group in HENNIG`s (1950) sense.

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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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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.