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Aim India is dominated by tropical grassy biomes (TGBs), traditionally considered seres or degraded forest, with low diversity relative to the restricted, ancestral wet zone. It is unclear if Indian grasslands and other open habitats are anthropogenically derived or native, old-growth habitats; without a clear timescale of grassland evolution. One way to understand grassland evolution is to study the diversification in taxa restricted to open habitats. We use a dated phylogeny of Ophisops to address questions related to the origin, diversification and inter-relationships of Indian and Saharo-Arabian Ophisops, and ultimately the origin of Indian grasslands and open habitats. Location The Indian subcontinent; the Saharo-Arabian Realm. Methods We generated up to 2736 base pairs of aligned sequence data (one mitochondrial, two nuclear genes) for Indian lacertids and reconstructed phylogenetic relationships using maximum likelihood and Bayesian inference. We use a fossil-calibrated timetree, diversification analyses and ancestral area reconstructions to test the hypotheses of origin and relationships with Saharo-Arabian Ophisops. Results Ophisops is strongly supported as monophyletic, with a basal split into a large-bodied (LBC) and small-bodied clade (SBC). The Saharo-Arabian species are nested within the Indian species in the LBC. Species diversity in Indian Ophisops is grossly underestimated, with 26–47 candidate species. Ophisops began diversifying in the late Oligocene with significant rate shifts in the late Miocene-Pliocene and Pleistocene within the SBC. Main conclusions Our results are consistent with an ancient origin of grassland taxa and TGBs in India. Ophisops is a dramatic example of overlooked cryptic diversity outside forests, with ~30 species where five were known. Ophisops dispersed into India from the Saharo-Arabian Realm in the Oligocene with a back dispersal in the Middle Miocene, a novel biogeographical pattern. Diversification in the SBC of Ophisops increased 8-fold during the global C4 grassland expansion. Indian TGBs are old-growth ecosystems that need urgent conservation attention.

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

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

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

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This paper deals with the reptile fauna of Gujarat State, and is primarily based on a collection made by the author during the Gujarat survey between 1989-1993. Information from earlier collections from Gujarat in the Zoological Survey of India, have also been included, as are data from the literature. To increase the usefulness of the paper, species that have ranges approaching the State have also been included. Altogether, 66 species in 50 genera and 18 families that are known from Gujarat have been dealt with in this report. Keys, diagnostic characters, measurements and distributional notes have been incorporated in the paper. Two squamate species, Hemidactylus triedrus and Lygosoma lineata are being reported for the first time from Gujarat.

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This paper presents a herpetofaunal inventory of the urban city of Ujjain, Madhya Pradesh along with major threats existing in the study area, snake-human conflict and conservation steps taken. Herpetofaunal population in degraded while urban habitat is essential for their long term conservation measures. A total of 39 species of reptiles and amphibians representing 15 families were detected with special account of Argyrogena fasciolata, Wallophis brachyurus, Lycodon aulicus, Ptyas mucosa, Xenochrophis piscator, and Lygosoma lineatum. Snakes were the most collected reptilian species, while Amphibians comprised the little group of the sample. Reptile Conservation & Research Centre is established in the city by Sarpa Anusandhan Sangthan to minimize the snake-human conflict and to educate and familiarise people with them.

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

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The Gulf of Kachchh is endowed with a variety of habitats and supports diverse groups of fauna, both invertebrates and vertebrates. The present study was carried out to study distribution of marine and coastal herpetofauna (Amphibians and Reptiles) from the Gulf of Kachchh (GoK). During the study a total of 28 species of herpetofauna were recorded from the GoK, of which, 3 were amphibians (only Anuran) and 25 were reptiles. Among the all recorded species, five species such as Green Sea Turtle, Olive Ridley, Yellow Sea Snake, Annulated Sea Snake and Gerard’s Mud Snake were obligatory marine reptiles. In addition, three other species viz., Saw-scaled Viper, Fringed-toed Lizard and Jerdon’s Snake eye were also r

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This study was conducted to see whether herpetofaunal assemblage differed amongst hiking trails, undisturbed forest and urban areas within the Margalla Hills National Park, Islamabad Capital Territory, Pakistan. Circular plot area-constrained searches (45 plots in each habitat, each plot with an area of 25 m2) were used from March 2018 to July 2019. We recorded seven amphibian species, nine lizard species and six snake species. The species richness of amphibians and lizards was the same in the studied strata, while the detection and encounter rate of snakes was lower in the undisturbed forest and urban areas. The encounter rate of amphibians differed significantly between urban areas and hiking trails/undisturbed forest. The encounter rate and population density of lizards differed significantly between undisturbed forest and urban areas. The most frequently encountered amphibian species along the hiking trail and urban areas was Duttaphrynus stomaticus, with Hoplobatrachus tigerinus in undisturbed forest. The most common and frequently encountered lizard species along the hiking trail and urban areas was Hemidactylus brookii, while the Ophisops jerdonii was the most frequently seen in undisturbed forest. The most common and frequently encountered snake species along the hiking trail and undisturbed forest was the Indotyphlops braminus, while Ptyas mucosa was the most common in urban areas. The subsequent bio-assessment, based on herpetofauna, of the Park revealed good to excellent biotic integrity The Park faces threats including livestock grazing, alien invasive vegetation and human disturbance due to settlements, restaurants and tourism-related activities. While several of these threats have been mitigated since the establishment of the Islamabad Wildlife Management Board, the Park still requires improved management, especially regarding regulating tourism.

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

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We present an inventory of the herpetofauna of the Nallamala Hills, Eastern Ghats, south-eastern India. The fauna, as currently known, includes 20 species of amphibians belonging to 14 genera in six families and 64 species of reptiles belonging to 42 genera in 15 families. Divided in habitat types, the herpetofauna can be classified into species tolerant of disturbed habitats; exclusively scrub species (and for reptiles, from rocky biotopes); scrub and bordering agricultural fields; and exclusively mesic forest species. For one species, lack of ecological information precludes its allocation to a specific habitat category. Significant diversity of squamates (including gekkonids, scincids, and colubrids) are known from these ranges, several of which endemic or largely restricted to scrub forests of Peninsular India. Mesic forests remain poorly explored, and support hitherto undescribed species among the herpetofauna. Adaptations seen amongst the herpetofauna of the Nallamala Hills include a diversity of dietary and habitat types, including, among amphibians, ant specialists; predators of small vertebrates; folivores; fossorial; terrestrial; aquatic or aquatic-margin; and arboreal forms. Amongst reptiles, adaptive types includes ant- and worm-eaters; predator of crop pests; predator of small or medium-sized vertebrate prey; egg-predators; fish-eaters; frog- and toadeaters; and one near-exclusive snake-eater. In terms of habitat usage, reptiles exceed amphibians in species richness, on account of their greater capacity of surviving in relatively arid regions. The Eastern Ghats contributes significantly to both species richness and endemicity of the Indian region, including representatives of endemic genera and species. Nonetheless, these hills continue to receive less attention for conservation compared to the relatively better-known Western Ghats.

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Over the past two decades many checklists of reptiles of India and adjacent countries have been published. These publications have furthered the growth of knowledge on systematics, distribution and biogeography of Indian reptiles, and the field of herpetology in India in general. However, the reporting format of most such checklists of Indian reptiles does not provide a basis for direct verification of the information presented. As a result, mistakes in the inclusion and omission of species have been perpetuated and the exact number of reptile species reported from India still remains unclear. A verification of the current listings based on distributional records and review of published checklists revealed that 199 species of lizards (Reptilia: Sauria) are currently validly reported on the basis of distributional records within the boundaries of India. Seventeen other lizard species have erroneously been included in earlier checklists of Indian reptiles. Omissions of species by these checklists have been even more numerous than erroneous inclusions. In this paper, I present a plea to report species lists as annotated checklists which corroborate the inclusion and omission of species by providing valid source references or notes.

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The composition and distribution of the vertebrate fauna of Afghanistan remain poorly documented and in recent decades little new data have become available due to a series of wars and the resulting unstable security conditions. As Afghanistan returns to some semblance of normalcy, baseline faunistic data will be particularly important for establishing national conservation priorities as well as for placing Afghan taxa into their broader phylogenetic and zoogeographic contexts. We here provide an updated checklist of the herpetofauna of Afghanistan based in part upon biodiversity archives of specimen records from several museum and private collec- tions as well as literature references and field research. The herpetofauna of Afghanistan consists of 118 species and subspecies belonging to 58 genera and 21 families. Seven species are endemic to the country, whereas 18 taxa have to be delet- ed from previous lists of the Afghan herpetofauna. Afghanistan’s primary zoogeo- graphic relationship to the Palearctic Region is reaffirmed but with secondary influ- ence from the Oriental Region. Immediately following the checklist, two sections provide information about species probably occurring in Afghanistan and previous- ly mentioned species that are now recognized as absent.