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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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Field notes and vivarium observations on Philochortus zolii are given as contribution to the biology of this little-known genus of lacer-tids. These concern the activity rhythm, food preferences, weights and sizes and coloura-tion of the five captive specimens. The largest specimen had a maximum snout-vent length of 61 mm, a tail length of 190 mm and weighted 6.24 g. Unhappily no reproduction was recorded, which very well may have been caused by a lack of adult males. Possible ovi-position occurred in the vivarium in July 2009. The annual activity was lowest in November to February; in the warmer months the daily activity peaked with the start focused around 10-12 o`clock, in later years this shifted to 14-17 o`clock because of the position of the vi-varium when the lizards could profit from the sunshine coming from the south-west. The curious way the Philochortus walk with the dorsal side up on the gauze cover of their cage, is described and discussed, as is their locomotion in the vivarium.

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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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The checklist is based primarily on extensive collections made by the United States Naval Medical Research Unit No. 3 (NAMRU-3) in Egypt. Forms listed are those that are known or expected to occur in Egypt (including Sinai), and those that have been reported from Egypt without further verification. The systematic lists contain original citations, references to major faunal works, and the most recent reviews of each particular group. From the 3.424 specimens obtained, adequate distributional data are now available for most forms in Egypt. Maps showing collecting localities for each species are also presented for use in future sympatric and ecological studies.

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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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Philochortus zolii is a globally endangered lizard known only from five localities scattered across North Africa. The population is thought to be decreasing, but there are almost no data about this Sahara-Sahel endemic lizard. Recently, a sixth population was found in Mauritania, at the coastal peripheral zone of the Diawling National Park, which constitutes a remarkable opportunity to gather ecological information for the first time and to plan conservation actions. Here we assess the P. zolii regional distribution in Mauritania, estimate population abundance, analyse the species activity patterns, characterise the occupied habitats, assess local threats, evaluate the national conservation status, and define an action plan for the local conservation of the species. P. zolii is locally rare and exhibits a much-localised distribution, but additional sampling is needed in other humid areas to fill out the knowledge gap on global distribution. The activity period is very restricted, limited to the central hours of the day, with low detectability and high specialisation in habitat use. The species is evaluated as Critically Endangered at the national level and is threatened by industrial and agriculture developments. These activities have degraded the suitable available habitats and hamper any dispersal possibility. Extreme climatic events related with sea-level rise could decimate the entire Mauritanian population. Any pet trade that may be stimulated by the current discovery should be carefully supervised and monitored. The discovery of this isolated population justifies that coastal habitats should be designated as integral protection zone and included inside the Diawling National Park.

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Evaluating flagship species and their potential for biological preservation and ecotourism development is a key issue for many audiences within the conservation and social fields. Despite several methods available to identify flagships, their application is often constrained in remote, poorly studied regions. Developments are needed in statistical and spatially-explicit approaches to assess species` traits influencing flagship appealing, to identify flagship fleets, and to map the location of flagship hotspots. Here, we developed a new method to identify flagship species in regions with knowledge gaps, using a two-stage statistical approach (ordination and clus- tering algorithms) to assess variable`s contribution to appealing and to group species sharing similar char- acteristics into flagship fleets. We then mapped areas concentrating the highest richness of flagships. Unique morphologies and behaviours, conservation status, endemicity, body size and weight, and feeding habits were the traits contributing the most to the flagship appealing. Nine flagship fleets were identified, from which two were the most suitable for conservation marketing and ecotourism promotion campaigns in Sahara-Sahel: Fleet A comprising 36 large-bodied species (18 mammals, 18 reptiles) and Fleet B including 70 small-bodied species (10 birds, six mammals, 54 reptiles). A total of 19 and 16 hotspots were identified for large-bodied and small-bodied flagships, respectively. The methodology was suitable to identify flagship species for conservation marketing and for developing ecotourism operations in the Sahara-Sahel, to independently assess which species` traits are re- levant for flagship appealing, and to organise fleets for multispecies-based marketing campaigns. The framework is scalable and replicable worldwide.

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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.