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This study includes a list of reptiles collected from Rumaila desert, south of Iraq, with a redescription of snake Eryx jayakary were given.

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

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In this study, we identified the diversity of the freshwater, marine and terrestrial herpetofauna of the State of Kuwait. It consists of a total of 45 extant species; 44 species of reptiles and a single species of amphibian according to recent updated taxonomic studies. All specimens of reptiles collected and held in American and European natural history museums are documented. Four species are added to the herpetofauna of Kuwait: Chalcides ocellatus, Hydrophis lapemo ides, Hydrophis viperina, and Trapelus agnetae.

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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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Aspects of the ecology of 23 lizard species found in the coastal lowlands of eastern Arabia are reported. Most forms occur in arid environments. The most obvious ecological separation is between diurnal and nocturnal species, the 10 latter all being geckos. Within these 2 groupings, species differ principally in microhabitat (particularly such features as distance from vegetation and ground softness), hunting techniques (sit and wait, active search or slow visual scanning) and the size of their mainly arthropod prey. However, 2 large diurnal forms are food specialists, feeding largely on plants and small vertebrates, respectively, and some diurnal species show differences in time of activity during morning. Body temperature of day-active species is controlled by posture, retreat into shade or burrows and use of the ground as a heat sink. Most nocturnal forms have body temperatures close to the ambient but they may sometimes be elevated in Bunopus tuberculatus, perhaps as a result of utilizing underground warmth. A wide range of predator avoidance techniques is used. Females are mainly gravid in spring. The number of eggs carried is low in species of small body size (often 1-2), suggesting that egg-laying is repetitive. Gross body shape is related to hunting and escape technique, foot structure to substratum type, and species living on soft sand have modifications that exclude sand from body orifices.

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The ability to shed (autotomize) all or part of the tail, usually in response to predator attack, and often to subsequently regenerate it is widespread in lizards and amphisbaenians and also occurs in a few snakes and in the tuatara. Most species possess a sophisticated intravertebral autotomy mechanism which seems to be primitive in the Squamata. This appears to have been independently lost in members of many groups, but some agamids and snakes have regained the ability to shed their tails by a simpler intervertebral means and a -number of agamids have also redeveloped tail regeneration as well. Breakable tails are used to evade capture in two main ways: by enabling reptiles to break away from predators that have grasped them by the tail and by providing a distraction which deflects the attention of the attacker away from the vulnerable head and body. It is argued that loss of caudal autotomy has occurred when the costs of tail shedding outweigh its benefits. Likely costs include the expense of regrowing the tail and the loss of a variety of possible tail functions that may cause partial incapacitation, at least until the tail regenerates. Benefits of autotomy are liable to be low if predation is rare, if the animal is able to protect itself effectively in other ways, if it is too slow to evade further pursuit after the tail is shed, or if the tail is small or unpalatable and consequently not likely to distract a predator. Benefit variation may well be greater than cost variation and therefore more important in initiating the loss of autotomy mechanisms. Many taxa that do not shed the tail appear to conform to the above interpretation, but in some cases, such as the Platynota, Agamidae and Chamaeleonidae, lack of intravertebral autotomy may reflect the history of these groups rather than being a direct result of present ecological pressures. The distribution of intervertebral autotomy in the Agamidae suggests that it may have evolved only in rather special circumstances where tail fragility is advantageous even in the absence of the ability to regenerate. Restriction ot autotomy planes to the tail-base, so that the whole organ is lost, a condition found in a number of relatively slow-moving geckoes, is interpreted as a means of ensuring that enough of the tail is shed to distract a predator from further pursuit. The stimulus necessary to induce autotomy can vary rapidly in individual lizards and at least some of these changes probably maximize the effectiveness of the tail-shedding mechanism. Differences in the readiness with which all or part of the tail is shed exist between species and are likely to reflect the balance of costs and benefits in particular cases. Variations in incidence of broken tails between species and populations may be due to such differences in fragility but many other factors may play a part, including the age structure of samples, incidence of unsuccessful attacks by predators and ability to evade predators after autotomy. There is a clear tendency for climbing lizards, especially those living on rock surfaces, to have higher incidences of broken tails than ground-dwelling species, perhaps because the tail is usually less important in locomotion in the first group. Many lizards possess conspicuously coloured tails and tail movements that seem likely to help distract attention from the head and body. Conspicuous tail colouring is more frequent and often better developed in young animals, which tend to be more vulnerable than adults, and in active species from open habitats where crypsis may not always be very effective. Conspicuous tails usually have contrasting light and dark areas in nocturnal forms but are often a single bright colour in diurnal ones, probably reflecting the visual capacities of their respective predators. The predominance of blue tails in day-active species may be because this colour is striking close to but not very arresting at a distance, so it may not attract predators from far away while still drawing their attention at close quarters.

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

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A key and check list is provided to the 96 species and six additional subspecies of lizards and two species of amphisbaenians known to occur in and around Arabia. Philochortus neumanni, Lacerta jayakari, Lacerta cyanura, Latastia longicaudata andersonii, Mesalina guttulata, Mesalina olivieri, Mesalina martini, Mesalina brevirostris, Mesalina ayunensis, Mesalina adramitana, Acanthodactylus orientalis, Acanthodactylus robustus, Acanthodactylus opheodurus, Acanthodactylus boskianus, Acanthodactylus felicis, Acanthodactylus yemenicus, Acanthodactylus masirae, Acanthodactylus opheodurus, Acanthodactylus gongrorhynchatus, Acanthodactylus haasi, Acanthodactylus schmidti, Acanthodactylus blanfordii, Acanthodactylus arabicus, Acanthodactylus grandis, Acanthodactylus tilburyi, Acanthodactylus scutellatus hardyi.

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The structure of copulatory organs is used very widely in systematics, both for differentiating species and for working out relationships. Differences between taxa may arise from a variety of sources, including non-homology, differences in other parts of the animal, direct selection on copulatory organs, development of physical isolating mechanisms and pleiotropic events. Physical isolating mechanisms seem likely to account for the abrupt differences, involving size, asymmetry and simplifications, that are useful in distinguishing very similar lacertid species. Although these differences usually seem to arise at the end of a speciation event they can simultaneously be the initiating mechanism in a second one. Copulatory organs appear to have high inherent stability, probably resulting from frequent location in strongly homoeostatic environments, single function, insensitivity to niche shift and inertia due to the need to conform to the genitalia of the opposite sex. This stability may be overridden at times by direct selection on the organs themselves or pleiotropic events. Such changes tend to be retained because efficiency in copulation depends not on any absolute genital architecture but on close conformity of the organs. It is the combination of relative stability and tangible input of varied change, which tends to be retained, that so often makes these structures good indicators of relationship.

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Arabia, including the arid lowland regions of Jordan, Syria, Iraq and southwest Iran, has approximately 128 species of terrestrial reptiles and about 7 of amphibians. Endemicity is high, 55% of species being largely or entirely confined to the area. Abrupt faunal discontinuities are present between Arabia and neighbouring regions, namely the Horn of Africa, the Sahara desert and the relatively mesic areas to the north. However, there must have been substantial interchange with these areas in the past. Within Arabia, the main Zoogeographie division is between the arid regions occupying most of the peninsula and much smaller, often more mesic areas of endemicity in the south. The former are mainly occupied by Saharo-Sindian taxa and have rather more affinities with the Sahara than to arid regions east of Arabia. Southern areas of endemicity include: 1. The southwestern coast, with affinities to the Horn of Africa and the inland deserts of Arabia. 2. The southwest and southern highlands which share a number of forms with northeast African relationships but differ significantly, the former having more, often endemic species with African affinities and a number with relatives in the Mediterranean and other northern mesic regions. The drier southern mountains have their own endemics, some of which have representatives in the öiddat al-HaräsIs area to the east. 3. The north Oman mountains also possess distinctive species and populations, some of which are related to forms in the less arid parts of the Iranian area. Finally there are a number of mesic forms distributed around the periphery of Arabia, and populations at oasis sites in the arid region which are probably relicts of forms more widespread in Quaternary pluvial phases.

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

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Die Vorliegende Studie belegt das Vorkommen von Mesalina brevirostris BLANFORD, 1874 in der Türkei. Neun Exemplare (fünf Männchen, vier Weibchen) wurden in Akçakale (Sanliurfa) nahe der türkisch-syrischen Grenze am 6 und 7. Mai 2002 gefangen. Die Pholidosemerkmale der neun Exemplare aus Akçakale ähneln denen, wie sie mehrere Autoren für syrische Tiere angeben. Die Anzahl der Dorsalia-Querreihen ist bei den Exemplaren von Akçakale (49,0 - 57,0; Mittelwert 53,2) deutlich größer als bei Tieren aus dem östlichen und zentralen Syrien (36,0 - 47,0; Mittelwert 40,3). Nach metrischen, meristischen und Farbmuster-Merkmalen sind die neun Exemplare von Südost-Anatolien der typischen Form Mesalina brevirostris brevirostris zuzuordnen.

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

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The ultrastructure of the nuclei in the ovarian follicular cells has been examined in the lizards Acanthodacylus scutellatus hardyi, and Eremias brevirostris. During certain growth stages, the nuclei of the intermediate and the pyriform cells become large and conspicuous, and usually contain numerous morphologically variable nucleoli. The latter may be nucleolonemal, compact, ring-shaped, “filamentous”, “fine-filamentous”, “amorphous” or “course-granular” in type, and the number and type in each nucleus seems to be related to the developmental stage. The type of nucleolus may indicate different phases of activity in the nucleus and may also suggest an association with the production of different types of RNA.

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A phylogenetic-comparative approach was used to assess and refine existing secondary structure models for a frequently studied region of the mitochondrial encoded large subunit (16S) rRNA in two large lizard lineages within the Scincomorpha, namely the Scincidae and the Lacertidae. Potential pairings and mutual information were analyzed to identify site interactions present within each lineage and provide consensus secondary structures. Many of the interactions proposed by previous models were supported, but several refinements were possible. The consensus structures allowed a detailed analysis of rRNA sequence evolution. Phylogenetic trees were inferred from Bayesian analyses of all sites, and the topologies used for maximum likelihood estimation of sequence evolution parameters. Assigning gamma-distributed relative rate categories to all interacting sites that were homologous between lineages revealed substantial differences between helices. In both lineages, sites within helix G2 were mostly conserved, while those within helix E18 evolved rapidly. Clear evidence of substantial site-specific rate variation (covarion-like evolution) was also detected, although this was not strongly associated with specific helices. This study, in conjunction with comparable findings on different, higher-level taxa, supports the ubiquitous nature of site-specific rate variation in this gene and justifies the incorporation of covarion models in phylogenetic inference.

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We have updated the list of the lizard species present in Qatar and produced the first distribution maps based on two field surveys in 2012 and 2013. We used the QND95/Qatar National Grid with a grid of 10 × 10 km squares for mapping. Our results show the occurrence of 21 lizard species in Qatar, from the 15 species indicated in the last biodiversity report conducted in 2004. The most abundant family found in Qatar is Gekkonidae with nine species (Bunopus tuberculatus, Cyrtopodion scabrum, Hemidactylus robustus, H. flaviviridis, H. persicus, Stenodactylus arabicus, S. slevini, S. doriae, Pseudoceramodactylus khobarensis), followed by Lacertidae with four species (Acanthodactylus schmidti, A. opheodurus, Mesalina brevirostris, M. adramitana), Agamidae with three species (Trapelus flavimaculatus, Uromastyx aegyptia, Phrynocephalus arabicus), Scincidae with two species (Scincus mitranus, Trachylepis septemtaeniata), and Varanidae (Varanus griseus), Sphaerodactylidae (Pristurus rupestris) and Trogonophiidae (Diplometopon zarudnyi) with one species each. The species richness fluctuated largely across Qatar between one and eleven species per grid square. We believe that the lizard fauna records in Qatar are still incomplete and that additional studies are required. However, our study here fills a gap concerning lizard biodiversity knowledge in the Gulf Region.

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

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The terrestrial reptiles oft he UAE the lizards, snakes and a single species of amphisbaenian or worm lizard. There are no extant native crocodiles, tortoises or freshwater terrapins. Lizards, snakes and amphisbaenians are all classified under the reptilian order Squamata, in the suborders Sauria, Serpentes and Amphisbaenia respectively. Characterised by their dry, scaly skin, which protects them from drying out, and by their reliance on external heat sources to maintain their body temperatures, reptiles are well-suited to hot and arid areas. In Arabia, reptiles are a major component of the desert and mountain ecosystems and a total of at least 54 species of terrestrial reptile are found in the UAE. So far, a comprehensive handbook covering all of the UAE reptiles in detail is not available. The Handbook to Middle East Amphibians and Reptiles (Leviton et al. 1992) does not cover the species of the mountains or Northern Emirates and gives little information on natural history. Useful general sources of information are Wild about Reptiles (Jongbloed 2000) and Terrestrial Reptiles of Abu Dhabi (Baha El Din 1986).

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Une comparaison de l`herpétofaune du Maroc et de la Jordanie est esquissée. Ces deux pays ont été choisis parce qu`ils se situent aux extrémités ouest et est de la Méditerranée, et que j`ai eu l`opportunité d`y séjourner plusieurs fois. Bien que distants de 3 700 km l`un de l`autre, ces deux pays présentent de nombreuses affinités dans la composition de leurs herpétofaunes respectives. Ceci est dû entre autres à des configurations géographiques en partie comparables. En revanche, l`isolation des plaines de l`ouest Marocain par les chaînes de l`Atlas et l`influence océanique très marquée ont favorisé la persistance d`espèces relictuelles endémiques et la différentiation d`espèces distinctes de part et d`autre de l`axe atlasique, alors que la Jordanie ne comporte aucune espèce endémique à ce seul pays. Enfin, le Maroc est presque huit fois plus étendu que la Jordanie, ce qui n`est pas négligeable quand on s`intéresse à la richesse spécifique d`un pays. En effet, le Maroc compte au moins 119 espèces d`amphibiens et de reptiles et la Jordanie, 100 espèces. Dans l`état actuel des connaissances taxonomiques, 13 espèces sont encore considérées comme les mêmes au Maroc et en Jordanie, presque toutes cependant représentées par des sous-espèces bien différenciées et/ou par des lignées très divergentes. Trente-deux genres sont communs aux deux pays, dont beaucoup sont des taxons des régions arides et désertiques, zones toutes plus ou moins reliées entre elles et non séparées par des barrières géographiques très anciennes. Vingt-sept genres présents au Maroc sont inconnus en Jordanie et 24 genres présents en Jordanie sont inconnus au Maroc. Contrairement aux similitudes des deux herpétofaunes, les différences sont surtout marquées chez les espèces méditerranéennes, auxquelles se joignent quelques éléments afro-tropicaux absents de Jordanie. Plusieurs exemples de couples d`espèces Maroc / Jordanie ont été commentés sur la base de photos originales prises dans les deux pays. Le genre Mesalina a fait l`objet d`une attention particulière, avec la mise en évidence de deux espèces supplémentaires pour la Jordanie: Mesalina bahaeldini et M. microlepis.

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

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We report observations on the natural history of lizards in the Gando Protected Area, within the Sistan and Baluchestan Province, Iran. The identity of the lizards is recorded, along with remarks on some meristic characteristics. Brief descriptions of their habitats are also given with a distribution map. Lizards (n = 132) were collected and photographed in 2008-09. Twelve species belonging to 9 genera and five families were found: Agamidae: Laudakia melanura lirata, Trapelus agilis, Laudakia fusca; Gekkonidae: Bunopus tuberculatus, Cyrtopodion scabrum, Hemidactylus persicus, Hemidactylus flaviviridis; Lacertidae: Mesalina brevirostris, Mesalina watsonana, Acanthodactylus blanfordi; Scincidae: Eumeces schneiderii zarudnyi; Varanidae: Varanus griseus caspius. This is the first record of Mesalina brevirostris in southeastern Iran.

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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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In this study we review the species of lizards in the genus Mesalina (Lacertidae) and present a new key for their identification. We also obtained five photos of each species from the British Museum of Natural History that illustrate the dorsal, lateral (right and left), and ventral views of the head and the femoral pores of each species. The papers with the original descriptions of each species were reviewed and used in preparation of the key. Some remarks about the habitat, natural history, updated distribution map and previous taxonomic changes are explained.

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The Afrotropical element in the Arabian herpetofauna is concentrated in the southwestern mountainous region, whereas everywhere else in the peninsula the reptile fauna is Saharo-Sindian. There is a high degree of correspondence between the reptile faunas of the Yemens and Somalia. A remarkable faunistic resemblance also exists between the relict faunas of SW Arabia and Morocco. Three evolutionary levels can be distinguished among Ethiopian taxa in Arabia and are interpreted as evidence of different times of faunal contact: 1. Old relicts (genus level) of a Palaeogene (pre continental drift) Arabian/North African fauna (Pristurus, Trogonophidae); 2. Endemic species closely related to East African species (most probably Miocene); 3. Species distributed on both sides of the Bäb al-Mandab (Pleistocene). Contrary to the Saharo-Sindian faunal elements, there is good evidence that groups 2 and 3 used a landbridge across the Bäb al-Mandab for faunal exchange: the Miocene closure of the southern outlet of the Red Sea and a Pleistocene land connection due to eustatic sea level change.

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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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Mesalina is a widespread lacertid genus occurring throughout the Saharo-Sindian region from North Africa to Pakistan. It has been through a series of taxonomic revisions, but the phylogenetic relationships among the species remain unclear. In this study we estimate the phylogeographic structure of M. guttulata across most of its distributional range and we evaluate the relationships between M. guttulata and the sympatric species M. brevirostris and M. bahaeldini using partial mitochondrial DNA (mtDNA) sequences (cyt b and 16S). M. guttulata and M. brevirostris represent species complexes, whereas M. bahaeldini considered before as M. guttulata is a recently described species with very restricted distribution. Here we present the first evidence that M. guttulata is a paraphyletic taxon with respect to M. bahaeldini, while M. brevirostris proves to be a polytypic species or even a species complex, confirming previous studies. Although mtDNA markers have several properties that make them suitable for phylogeographic studies, they are not free of difficulties. Phylogeographic inferences within and between closely related species can be mislead by introgression and retention of ancestral polymorphism (incomplete lineage sorting). However, the present distribution pattern, the estimated times of divergence and the significant variation in morphology within M. guttulata led us to accept that the paraphyletic pattern observed, is most likely due to inaccurate taxonomy. Our hypothesis is that what has hitherto been considered as intraspecific variation, actually reflects species-level variation. Furthermore, our biogeographic analyses and the estimated time of divergences suggest that the present distribution of M. guttulata was the result of several dispersal and vicariant events, which are associated with historical changes (climatic oscillations and paleogeographic barriers) of late Miocene and Pliocene period.

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During recent years several lizard taxa were added to the faunal list of Pakistan. Descriptions and new records are scattered in different publications in the herpetological literature. The present paper puts the information together, and provides a comprehensive list of recent publications on the lizards of Pakistan.

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Aim To map and assess the richness patterns of reptiles (and included groups: amphisbaenians, crocodiles, lizards, snakes and turtles) in Africa, quantify the overlap in species richness of reptiles (and included groups) with the other terrestrial vertebrate classes, investigate the environmental correlates underlying these patterns, and evaluate the role of range size on richness patterns. Location Africa. Methods We assembled a data set of distributions of all African reptile species. We tested the spatial congruence of reptile richness with that of amphibians, birds and mammals. We further tested the relative importance of temperature, precipitation, elevation range and net primary productivity for species richness over two spatial scales (ecoregions and 1° grids). We arranged reptile and vertebrate groups into range-size quartiles in order to evaluate the role of range size in producing richness patterns. Results Reptile, amphibian, bird and mammal richness are largely congruent (r = 0.79–0.86) and respond similarly to environmental variables (mainly productivity and precipitation). Ecoregion size accounts for more variation in the richness of reptiles than in that of other groups. Lizard distributions are distinct with several areas of high species richness where other vertebrate groups (including snakes) are species-poor, especially in arid ecoregions. Habitat heterogeneity is the best predictor of narrow-ranging species, but remains relatively important in explaining lizard richness even for species with large range sizes. Main conclusions Reptile richness varies with similar environmental variables as the other vertebrates in Africa, reflecting the disproportionate influence of snakes on reptile richness, a result of their large ranges. Richness gradients of narrow-ranged vertebrates differ from those of widespread taxa, which may demonstrate different centres of endemism for reptile subclades in Africa. Lizard richness varies mostly with habitat heterogeneity independent of range size, which suggests that the difference in response of lizards is due to their ecological characteristics. These results, over two spatial scales and multiple range-size quartiles, allow us to reliably interpret the influence of environmental variables on patterns of reptile richness and congruency.

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

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Taxonomic changes and new findings concerning the subfamily Eremiainae in Africa are summarized to update SZCZERBAK`s (1975) catalogue of the African Sand Lizards. Furthermore, a key to the species and subspecies of the genus Pedioplanis is provided.

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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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Aim Temperature influences most components of animal ecology and life history – but what kind of temperature? Physiologists usually examine the influence of body temperatures, while biogeographers and macroecologists tend to focus on environmental temperatures. We aim to examine the relationship between these two measures, to determine the factors that affect lizard body temperatures and to test the effect of both temperature measures on lizard life history. Location World-wide. Methods We used a large (861 species) global dataset of lizard body temperatures, and the mean annual temperatures across their geographic ranges to examine the relationships between body and mean annual temperatures.We then examined factors influencing body temperatures, and tested for the influence of both on ecological and life-history traits while accounting for the influence of shared ancestry. Results Body temperatures and mean annual temperatures are uncorrelated. However, accounting for activity time (nocturnal species have low body temperatures), use of space (fossorial and semi-aquatic species are ‘colder’), insularity (mainland species are ‘hotter’) and phylogeny, the two temperatures are positively correlated. High body temperatures are only associated with larger hatchlings and increased rates of biomass production. Annual temperatures are positively correlated with clutch frequency and annual longevity, and negatively correlated with clutch size, age at first reproduction and longevity. Main conclusions Lizards with low body temperatures do not seem to have ‘slower’ life-history attributes than species with high body temperatures. The longer seasons prevalent in warm regions, and physiological processes that operate while lizards are inactive (but warm enough), make environmental temperatures better predictors of lizard life-history variation than body temperatures. This surprisingly greater effect of environmental temperatures on lizard life histories hints that global warming may have a profound influence on lizard ecology and evolution.

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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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Jordan has a very diversified morphology, which is reflected also in the diversity of its herpetofauna. A total 90 amphibian and reptilian species is known to inhabit Jordan. Of those three are amphibians, with the fourth species most probably already extinct, 47 are lizard species, 35 are snake species and five turtle species. The amphibians are represented by three different families, lizards and snakes both by seven families and turtles by four families. The distribution, ecology and systematics for most species are 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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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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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 genus Mesalina Gray 1838 is a holophyletic genus within the Lacertidae, mostly occurring in the Saharo-Sindian region as well as North Africa. This genus encompasses 13-14 species, 2-3 of which occurring in Iran. The Iranian species of Mesalina are as follows: Mesalina watsonana, M. brevirostris and, most likely, M. gutulatta. Of these, M. watsonana is widely distributed, occurring in most parts of the Iranian Plateau. Based on extensive study and research, systematics and distribution of the Iranian Plateau species of Mesalina are discussed and their distribution maps are given.

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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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In this paper, the evolution and ecology of directional asymmetry (DA) during the developmental trajectory (DT) is compared with that of its product, morphological DA (MDA). DT and MDA are calculated for two bilateral morphological scale characters of lizards, the number of subdigital lamellae beneath the fourth toe in 10 agamid and 28 lacertid taxa, and the number of rows of ventral scales in 12 lacertid taxa. MDA, the subtraction between left and right sides (classical measure of DA), is functional in adult animals. Results confirm the hypodiesis that, in DT, the regression parameters a (constant) and b (regression slope) of counts on the right side with those on the left describe a developmental process. No phylogenetic or environmental effects were observed on a and b, but analyses considering both a and b together show non-random phyletic patterns. Independent analyses deduced the same ancestral DT in Agamidae and Lacertidae. In Lacertidae, distance between pairs of taxa in a + b (standardized values) correlates positively with die phylogenetic distance between taxa. Phyletic trends in MDA are indirect, and due to the link of MDA with a + b. The MDA of species is more dissimilar in sympatry than in allopatry. The phyletic trends suggest evolution of DT, while die association of MDA witii sympatry suggests that ecological pressures shape MDA in adult animals. Evolution of DT is independent from tiiat of its product, MDA–adaptive determinism defines the result of, but not the mechanistic process of, development. Deterministic environmental processes define MDA, and deterministic evolutionary processes define the interactive result of a and b, but not each separately. According to circumstances, different DTs produce similar or different MDA, and a particular DT can produce different MDAs.

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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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Mesalina are small lacertid lizards occurring in the Saharo-Sindian deserts from North Africa to the east of the Iranian plateau. Earlier phylogenetic studies indicated that there are several species complexes within the genus and that thorough taxonomic revisions are needed. In this study, we aim at resolving the phylogeny and taxonomy of the M. brevirostris species complex distributed from the Middle East to the Arabian/Persian Gulf region and Pakistan. We sequenced three mitochondrial and three nuclear gene fragments, and in combination with species delimitation and species-tree estimation, we infer a time-calibrated phylogeny of the complex. The results of the genetic analyses support the presence of four clearly delimited species in the complex that diverged approximately between the middle Pliocene and the Pliocene/Pleistocene boundary. Species distribution models of the four species show that the areas of suitable habitat are geographically well delineated and nearly allopatric, and that most of the species have rather divergent environmental niches. Morphological characters also confirm the differences between the species, although sometimes minute. As a result of all these lines of evidence, we revise the taxonomy of the Mesalina brevirostris species complex. We designate a lectotype for Mesalina brevirostris Blanford, 1874; resurrect the available name Eremias bernoullii Schenkel, 1901 from the synonymy of M. brevirostris; elevate M. brevirostris microlepis (Angel, 1936) to species status; and describe Mesalina saudiarabica, a new species from Saudi Arabia.

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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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Aim: Deserts are generally perceived as areas of low diversity, and hence receive little attention from researchers and conservationists. Squamates are the dominant group of vertebrates in arid regions, and as such represent an ideal model to study biodiversity patterns in these areas. We examine spatial patterns of diversity, evolutionary history and endemism of terrestrial squamates of the Arabian Peninsula and test hypotheses on the role of topography and history of isolation so as to identify possible environmental drivers of diversification. Location: The Arabian Peninsula. Taxon: Squamate reptiles (Squamata; lizards and snakes). Methods: We generated distribution maps for all Arabian squamate species (including yet undescribed) and reconstructed their phylogenetic relationships using existing and newly produced genetic data for nearly all the species. We assessed patterns of the distribution of species richness, phylogenetic diversity and phylogenetic en demism across the peninsula to identify areas that could be considered evolutionary or endemicity hotspots for squamates. We evaluated community turnover across the peninsula and assessed the possible environmental drivers affecting the diversity of Arabian squamates in a regression framework. Results: The main hotspots of Arabian squamate diversity are mostly along the mountains that rim the peninsula while the most arid, central regions support a low diversity of species. The distribution of the phylogenetic diversity mirrors that of the species richness. Phylogenetic endemism is also highest in the mountains, especially when only endemic species are analysed. The deserts of northern Arabia are poor in terms of species richness and they show low connectivity to the peninsular communities. Topographic heterogeneity is the strongest predictor for Arabian squamates, followed by elevation. There is no correlation between richness and temperature. Main conclusions: The mountains of Arabia support rich and unique squamate communities that are dominated by local radiations of closely related and narrow-ranging species. In particular, the Asir Mountains of SW Arabia, Dhofar Province of Oman and the Hajar Mountains of northern Oman and UAE show unprecedented levels of squamate endemism and phylogenetic endemism. While many generalist species range across Arabia, a low number of species is shared between the peninsula and mainland Asia, indicating an effective isolation of the Arabian fauna. Squamate richness is highest in heterogeneous, topographically complex habitats.

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Five species of geckos (Bunopus tuberculatus, Crytodacylus scaber, Hemidactylus flavivirdis, H. turcicus, and Pristurus rupestris), one lizard species (Mesalina brevirostris) and three snake species (Eryx jayakari, Coluber ventromaculatus and Psammophis schokari) were recorded on a total of 13 islands during a herpetological survey conducted in 2003-2004 in the Arabian Gulf, Abu Dhabi Emirate. The distribution and abundance of these species is also described in detail. Bunopus tuberculatus and Mesalina brevirostris are more commonly distributed on the islands and the remaining gecko species are limited only to certain islands, whilst the three snake species were recorded only on one island.

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This paper provides an updated checklist of the United Arab Emirates (UAE) native and alien herpetofauna. The UAE, while largely a desert country with a hyper-arid climate, also has a range of more mesic habitats such as islands, mountains, and wadis. As such it has a diverse native herpetofauna of at least 72 species as follows: two amphibian species (Bufonidae), five marine turtle species (Cheloniidae [four] and Dermochelyidae [one]), 42 lizard species (Agamidae [six], Gekkonidae [19], Lacertidae [10], Scincidae [six], and Varanidae [one]), a single amphisbaenian, and 22 snake species (Leptotyphlopidae [one], Boidae [one], Colubridae [seven], Hydrophiidae [nine], and Viperidae [four]). Additionally, we recorded at least eight alien species, although only the Brahminy Blind Snake (Ramphotyplops braminus) appears to have become naturalized. We also list legislation and international conventions pertinent to the herpetofauna.

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The present paper of N. N. SZCZERBAK was originally published in Russian as `Katalog afrikanskih Jascurok` by the Academy of Sciences, Institute of Zoology, Museum of Zoology, USSR, Kiev (83 pp., 30 maps) in 1975. Lists of synonyms, bibliography, maps and table of contents - all being parts of the original paper - have not been included in this translation which was carried out with the consent of the author by R. GÜNTHER (Berlin) and H. GRILLITSCH (Vienna). The English summary was taken over as provided in the original version. As a SHORT NOTE in this issue of HERPETOZOA subsequent to the translation comments and updated addenda by W. MAYER are provided indicated by [aa* bb* etc.] in the text.

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The aim of this study was to determine if divergence in habitat use among lacertid lizards is paralleled by morphological differentiation. For 35 lacertid species, we measured body, head and limb dimensions. Habitat use was inferred from the literature: ground-dwelling on open terrain, ground-dwelling in vegetated areas, shrub-climbing, tree-climbing, saxicolous (i.e. rock-climbing). Traditional (i.e. non-phylogenetic) statistical analyses suggest morphological differences among species groups with different habitat use. Ground-dwelling species from open habitats tend to have longer femurs, tibiae and humeri (relative to body length) than other groups. Cursorial (i.e. level-running) species have relatively high heads and trunks compared to climbing species. These differences follow biomechanical predictions and it is tempting to consider tham as adaptations to habitat use. However, phylogenetic analyses of the data fail to establish a clear relationship between habitat use and morphology in the data set considered. There is a weak indication that the differences in head and trunk height have evolved as an adaptation to different habitat use, but the differences in relative limb dimensions among species groups with different habitat use vanish. Either adaptation of limb dimensions to habitat use has not occurred in lacertid lizards, or our methods are unable to demonstrate such an adaptation. We show that uncertainties in the topology of the phylogenetic tree used are unlikely to influence the outcome of our study. We also address the fact that habitat use is often similar in different branches of the phylogenetic tree, and the consequences this may have for the power of our statistical analyses.