×

Oman material of four lizard species is described and discussed ; it comprises specimens of a previously undescribed gecko, Phyllodactylus gallagheri, two lacertids — the poorly known Lacerta jayakari Boulenger, 1887, and L. cyanura, also described here for the first time, and a skink, Ablepharus pannonicus Lichtenstein, 1823. These species have no strong affinities with any members of the mainly Saharo-Sindian fauna now occupying much of Arabia but are closely related to forms occurring to the north of the peninsula. It is probable that they are relicts of a more temperate fauna which once entered more extensively into southeastern Arabia. As might be expected, all four species are absent from the desert areas of Oman and are confined to the disjunct mesic habitats which exist in the mountains.

×

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.

×

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.

×

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.

×

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).

×

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.

×

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.

×

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.

×

In this paper, we report on our failure to breed a lasting population of Omanosaura cyanura in a vivarium environment. In our vivaria, O. cyanura produced 1 – 5 (maximally 8) clutches per year with 2.5 – 3.5 eggs per clutch. The eggs grow to approximately 10.8 x 18.9 mm and weigh, on average, 1.29 g. The eggs normally hatch at 25 °C after 72 days and at 29 °C after 56 days. In this study, of the externally healthy looking, only approximately one third hatched. The average dimensions of the eggs immediately following oviposition were 6.0 x 10.8 mm with a mean weight of 0.25 g. We surmise that a potential reason for the lack of hatching success is a vitamin D3 deficiency. Raising the successful hatchlings (SVL 23.9 mm; TL 46.8 mm; weight 0.25 g) turned out to be quite difficult because they were very finicky about eating and drinking, and moreover turned out to be easily frightened. We recommend keeping the individual lizards separately most of the time because of a high level of interspecific aggression.

×

In the present work, we use an exceptional database including 5,359 records of 101 species of Oman’s terrestrial reptiles together with spatial tools to infer the spatial patterns of species richness and endemicity, to infer the habitat preference of each species and to better define conservation priorities, with especial focus on the effectiveness of the protected areas in preserving this unique arid fauna. Our results indicate that the sampling effort is not only remarkable from a taxonomic point of view, with multiple observations for most species, but also for the spatial coverage achieved. The observations are distributed almost continuously across the two-dimensional climatic space of Oman defined by the mean annual tempera- ture and the total annual precipitation and across the Principal Component Analysis (PCA) of the multivariate climatic space and are well represented within 17 out of the 20 climatic clusters grouping 10% of the explained climatic variance defined by PC1 and PC2. Species richness is highest in the Hajar and Dhofar Mountains, two of the most biodiverse areas of the Arabian Peninsula, and endemic species richness is greatest in the Jebel Akhdar, the highest part of the Hajar Mountains. Oman’s 22 protected areas cover only 3.91% of the country, including within their limits 63.37% of terrestrial reptiles and 50% of all endemics. Our analy- ses show that large areas of the climatic space of Oman lie outside protected areas and that seven of the 20 climatic clusters are not protected at all. The results of the gap analysis indi- cate that most of the species are below the conservation target of 17% or even the less restrictive 12% of their total area within a protected area in order to be considered adequately protected. Therefore, an evaluation of the coverage of the current network of protected areas and the identification of priority protected areas for reptiles using reserve design algorithms are urgently needed. Our study also shows that more than half of the species are still pending of a definitive evaluation by the International Union for Conservation of Nature (IUCN).

×

Th e terrestrial reptile fauna of Oman and the United Arab Emirates is rich, with at least 79 species of lizards and snakes and a single species of worm lizard. However, to date there have been no accurate maps published of their distribution ranges, and distribution data relies on scattered museum specimen localities and published accounts. Considerable numbers of locality data points do exist, collected by visting and resident herpetologists, and more recently, from ecologists working on surveys for environmental impact assessments and biodiversity action plans. Th ese data are invaluable, as amongst other uses, they can assist conservation planning and management, and will eventually document changes in distributions over time. Th is is especially true where there has been extensive habitat loss and degradation due to urbanisation and development activities. Data have been collected from museum records, published accounts and unpublished data from a variety of sources, including many records made by the author over the last 20 years, with the aim of producing an atlas of species distributions. Th e number of records is now approaching 5.000, giving suffi cient coverage to produce maps that are useful for a variety of applications. Examples are discussed, including endangered and endemic species, snakes of medical importance and species of potential interest in ecological and evolutionary studies.

×

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).

×

From the 26th of April until the 3rd of May I had a herpetological trip to Oman together with Javier Aznar, Javier Gallego and Gabriel Martinez. During these eight days we were able to find and photograph 48 reptile- and 2 amphibian species. The trip started in Maskat and took us by Al-Qabil, Thumrait to Salalah and back by Al-Qabil, Nizwa, Ibri, Barka to Maskat. The course of this journey is presented in chronological order.

×

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

×

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

×

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.

×

In this third paper on the herpetofauna of Oman, three families are treated: eleven Lacertidae, six Scincidae and one varanid. New records, notes on ecology and localities are combined with data from literature.

×

The herpetological results of three brief journeys to the saiq Plateau in the Sultanate of Oman are summarized. These yielded eight new locality records and numerous field observations. Existing distribution data are discussed relative to the new finds, and a checklist of recorded and expected species is presented.

×

The ecology, behaviour and first breeding of Lacerta cyanura are described. The breeding female laid three eggs every three weeks du- ring July to November. The first hatchlings were born after 59-61 days of artificial incuba- tion at 28°C. The colour pattern of hatchlings is entirely different from that of adults. The adults are dorsally light grey-brown, with a blue throat, white belly and a turquoise tail. The young have a black back and flanks with cream-yellow longitudinal stripes, a black and yellow marbled head, a very faintly yellowish or greenish underside, and a fluorescent blue tail. In contrast, the young of the presumed close relative Lacerta jayakari have almost the same colour pattern as the adults; this sug- gests a more distant relationship between the two species than has been assumed.

×

The rare Southeast Arabian lizard Lacerta cyanura ARNOLD, 1972 has been found at two additional localities (seven being actually known: GRUBER & al. 1993), which are both situated on the Musandam Pen- insula, Oman. Two males and one female are kept in captivity. The female, associated with only one of the males, so far produced 6 clutches of 3 eggs each in intervals oj roughly 3 weeks. This reproductive pattern and the juvenile dress are discussed, also in respect to the systematic relationship of this species.

×

The albumins from 41 species of the family Lacertidae representing a substantial part of genera as well as infrageneric groups of the collective genus Lacerta s.l. were investigated by means of the MCF technique. The data allow a chronological estimation of the most important radiation events and their correlation with paleogeographical facts. Our results are in remarkable contradiction to the phylogeny presented by ARNOLD (1989a) based mainly on morphological characters. The most important phylogenetic relationships are: 1. The genera Gallona and Psammodromus are already isolated from the other taxa since the Oligocene. We assess these main branches as subfamilies Gallotiinae and Lacertinae. 2. Lacerta s.str. and Lacerta subgenus Zootoca form the sister group of the remaining Lacertinae. 3. A colonization of Africa in the Lower Miocene has led to a separation in two lines, with mainly Eurasian and African members respectively. 4. ARNOLD`S (I.e.) `Ethiopian and advanced Saharo-Eurasian clade` proved to be a paraphyletic unit, one group of genera being more closely related to European taxa. All techniques applied to the systematics of Lacertidae hitherto are critically discussed. An area-time- hypothesis concerning the phylogeny of Lacertidae is presented. Key words: Lacertidae, phylogeny of; Gallotiinae subfam. nov.; Lacertinae subfam. nov.; micro complement fixation; albumin evolution.

×

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.

×

An increase in studies in the Hajar Mountains from the southeastern Arabian Peninsula has revealed a high richness of endemic evolutionary lineages with many cryptic taxa. Omanosaura is the only lacertid lizard genus endemic to the Hajar Mountains, with two species O. cyanura and O. jayakari distributed throughout this mountain range. The phylogenetic relationships and genetic diversity between and within these species have been poorly studied. In this study, we collected mitochondrial (12S, cytb, and nd4) and nuclear (cmos and mc1r) sequences for 25 specimens of Omanosaura, including 15 individuals of O. jayakari and 10 of O. cyanura. We performed phylogenetic analyses based on network reconstruction, maximum likelihood and Bayesian inference to estimate the relationships and intraspecific genetic diversity of these species. We estimated the time of divergence between the two species in the Miocene, around 8.5 million years ago. Omanosaura jayakari shows little genetic diversity, while O. cyanura presents two differentiated lineages. These are reciprocally monophyletic at mitochondrial and nuclear genes and present a high genetic distance between them. These two lineages are associated with the geographic features of the Hajar Mountains, with one lineage distributed in the northernmost part of the Hajar Mountains and the other in the rest of the western Hajars, the Jebel Akhdar, and the eastern Hajars. This geographic relationship has been recovered previously in other reptile taxa and is generally associated with high levels of local genetic diversity. Our results suggest the existence of cryptic diversity within O. cyanura and support a general biogeographic pattern of high diversity and endemism in the northern Hajar Mountains that certainly deserves additional research in the future.

×

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.

×

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.