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Abstract The Equatorial African group of lacertids comprises nine species which share a number of derived features and appear to constitute a holophyletic assemblage. Revision of the group using morphological characters analyzed by parsimony and compatibility methods results in the following taxonomic changes: Lacerta jacksoni = Adolfus jacksoni, Lacerta echinata = Gastropholis echinata, Bedriagaia tropidopholis = Gastropholis tropidopholis, Bedriagaia moreavi = Gastropholis prasina, the latter species being validated and removed from the synonymy of Gastropholis vittata. Adolfus jacksoni has most features in common with the hypothetical ancestor of the group, while Holaspis guentheri and the species of Gastropholis are the most derived forms. Geographical variation in Adolfus alleni is described and what is known of the ecology of the Equatorial group summarized. Most are forest dwellers with the majority of the more primitive forms living on tree boles and among litter and timber on the forest floor (Adolfus jacksoni, A. africanus, A. vauereselli). Another, Holaspis guentheri, is confined to tree boles but glides between them, while the species of Gastropholis appear to be climbers in flimsy vegetation and Adolfus alleni is ground-dwelling above the tree line. Many of the morphological features characterizing these lizards appear to be functionally related to their particular habitats.

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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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Phylogenies based on morphology vary considerably in their quality: some are robust and explicit with little conflict in the data set, whereas others are far more tenuous, with much conflict and many possible alternatives. The main primary reasons for untrue or inexplicit morphological phylogenies are: not enough characters developed between branching points, uncertain character polarity, poorly differentiated character states, homoplasy caused by parallelism or reversal, and extinction, which may remove species entirely from consideration and can make originally conflicting data sets misleadingly compatible, increasing congruence at the expense of truth. Extinction differs from other confounding factors in not being apparent either in the data set or in subsequent analysis. One possibility is that variation in the quality of morphological phylogenies has resulted from exposure to different ecological situations. To investigate this, it is necessary to compare the histories of the clades concerned. In the case of explicit morphological phylogenies, ecological and behavioural data can be integrated with them and it may then be possible to decide whether morphological characters are likely to have been elicited by the environments through which the clade has passed. The credibility of such results depends not only on the phylogeny being robust but also on its detailed topology: a pectinate phylogeny will often allow more certain and more explicit statements to be made about historical events. In the case of poor phylogenies, it is not possible to produce detailed histories, but they can be compared with robust phylogenies in the range of ecological situations occupied, and whether they occupy novel situations in comparison with their outgroups. LeQuesne testing can give information about niche homoplasy, and it may also be possible to see if morphological features are functionally associated with ecological parameters, even if the direction of change is unknown. Examination of the robust and explicit phylogeny of the semaphore geckoes (Pristurus) suggests that its quality does stem from a variety of environmental factors. The group has progressed along an ecological continuum, passing through a series of increasingly severe niches that appear to have elicited many morphological changes. The fact that niches are progressively filled reduces the likelihood of species reinvading a previous one with related character reversal. Because the niches of advanced Pristurus are virtually unique within the Gekkonidae the morphological changes produced are also very rare and therefore easy to polarize. Ecological changes on the main stem of the phylogeny are abrupt and associated character states consequently well differentiated. The small geographical distribution of the group reduces the chance of different forms entering the same niche and developing morphological parallelisms. Many species are represented because there are many refuge areas within the geographical distribution of Pristurus and also because the fact that niches are well differentiated reduces the chance of extinction by species competition. Examination of ten other lizard clades, mainly in the Lacertidae, shows that the historical features noted in Pristurus also occur in other groups with robust and explicit morphological phylogenies, such as Meroles and Gastropholis. On the other hand, they are often absent in assemblages where phylogenetic hypotheses based on anatomy are poorly supported or equivocal, for example Podarcis and Pedioplanis. The amount of alteration of genital features is not as closely associated with environmental factors as in many other morphological characters, possibly because ecological shifts do not affect them so directly and because they have their own special causes of change. This partial independence from the environmental factors that appear to control many characters means that genital features may enable some phylogeny reconstruction to be done, even when other systems are unhelpful. There is no evidence among the studied clades that groups with poor morphological phylogenies have inherent general constraints on the development and maintenance of new structural features. It seems that the quality of morphological phylogenies may give some indication of the kinds of history groups have had. Clearly, if the variety of ways in which evolution proceeds is to be understood, groups with both good and bad morphological phylogenies must be investigated.

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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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In this paper we deal on the ultraviolet color (invisible to us): where we can find it, the capability of animals to see it and the advantages that this color perception offers to them. As the simplest way to detect it is the photography, we describe and review how to photograph the UV, as a result of 15 years of amateur experience, searching and testing nearly in complete blindness due to the lack of practical information about “how to do it”. We describe the different kinds of photography (chemical and digital); the cameras and objectives suitable (both astronomically expensive ones and cheap options); what are the best characteristics that the objectives should have for this purpose; the films suitable for their use in chemical photography; the different filters (current or discontinued) manufactured along the years; and the subtle combinations among the different materials to obtain pure UV photographs. This kind of scientific photography is mainly used in forensics, forgery detection, art dermatology and less in Natural History, despite the fact that a great part of animals see this color and use it in important questions of their biology as the social behavior, mate choice or the food search.

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Animals communicate via a variety of sensory channels and signals. Studies on acoustic and visual communication systems suggest that differences in the physical environment contribute to the variety of signalling behaviour, with species investing in those signals that are transmitted best under the local conditions. Whether or not environmental tuning also occurs in chemical communication systems has received much less attention. In the present study, we examined the effect of several aspects of the physical environment on the chemical communication system of lacertid lizards (family Lacertidae). The numbers of femoral pores are used as a proxy reflecting how much a particular species invests in and relies upon chemical signalling. Femoral pores are specialized epidermal structures that function as a secretion channel for the waxy substance produced by glands. In some lacertid species, the secretion carries infochemicals that play an important role in social communication. The number of femoral pores varies considerably among species. We have compiled data on femoral pore numbers for 162 species and tested for the effects of climate and substrate use. After correcting for body size and taking the phylogenetic relationships among the species into account, we found no effect of climate conditions or latitude on species pore numbers. Substrate use did affect pore numbers: shrub-climbing species tended to have fewer femoral pores than species inhabiting other substrates.

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A complete catalogue is provided for the type specimens of lacertid lizards in the herpetological collection of the Zoological Museum, Berlin, as of December, 1993. The collection contains a total of 514 type specimens, representing 63 taxa, of which 42 are currently regarded as valid at the specific or subspecific level. Types representing an additional four taxa appear to have been lost from the collection. The collections are especially rich in African lacertid types and in historically significant specimens collected early in the Nineteenth Century by Pallas, Eversmann, and Hemprich & Ehrenberg. Also present are the type series of many subspecies of Podarcis lilfordi and P. pityusensis described by Eisentraut.

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Some notes are given on Gastroplwlis prasina based on the available literature. These arboreal lacertids, which were seen during a visit to the Bioken Snake Farm, were originally from the Arabuko Sokoke coastal forest, Kenya. This beautiful green lizard with a highly prehensile tail, seems perfectly adapted to life in the tree tops.

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Currently, four species of the lacertid lizard genus Adolfus are known from Central and East Africa. We sequenced up to 2825 bp of two mitochondrial [16S and cytochrome b (cyt b)] and two nuclear [(c-mos (oocyte maturation factor) and RAG1 (recombination activating gene 1)] genes from 41 samples of Adolfus (representing every species), two species each of Gastropholis and Holaspis, and in separate analyses combined these data with GenBank sequences of all other Eremiadini genera and four Lacertini outgroups. Data from DNA sequences were analysed with maximum parsimony (PAUP), maximum-likelihood (RAxML) and Bayesian inference (MrBayes) criteria. Results demonstrated that Adolfus is not monophyletic: Adolfus africanus (type species), Adolfus alleni, and Adolfus jacksoni are sister taxa, whereas Adolfus vauereselli and a new species from the Itombwe Plateau of Democratic Republic of the Congo are in a separate lineage. Holaspis and Gastropholis were recovered in separate clades. Based on these molecular data, relatively substantial sequence divergence, and multiple morphological differences, we describe a new genus of lacertid for the lineage including A. vauereselli and the new Itombwe species. The recognition of this new, endemic genus underscores the conservation importance of the Albertine Rift, especially the Itombwe Plateau, a unique region that is severely threatened by unchecked deforestation, mining, and poaching.

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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.

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The evolutionary diversification of many terrestrial vertebrate groups is strongly linked to climatic events in the Cenozoic, the period from 65 Million years ago to today when modern animals first appeared. I investigated the effects of Cenozoic climate change on the taxonomic and morphological diversification of the Old World lizard family Lacertidae, with particular emphasis on the African radiation. African lacertids exhibit an unusual pattern of diversification, in which their highest species richness occurs in deserts north and south of the equator, despite being spread throughout the continent. This disparity is particularly surprising given that desert lacertids are thought to be evolutionarily younger than their mesic-dwelling relatives, suggesting increased diversification rates in arid habitats. To identify the evolutionary factors underlying this pattern, I use a combination of phylogenetic, morphological and ecological techniques. In Chapter 1, I apply Bayesian methods and fossil-based calibrations to molecular sequence data to construct a time-calibrated phylogeny for Lacertidae. I estimate that the family arose in the early Cenozoic, with the majority of their African radiation occurring in the Eocene and Oligocene. In Chapter 2, I describe changes in lacertid body shape across biomes and substrates, and find widespread morphological convergence in similar habitat types. I suggest that in addition to foraging demands, fluctuating and extreme climatic conditions, largely driven by precipitation and temperature, contribute to morphological convergence across independent arid-dwelling clades. Finally, I test if ancestral transitions in ecology, morphology, and rates of diversification temporally coincide with paleoclimatic events in the Cenozoic. I use High Resolution X-ray Computed Tomography to characterize changes in the skull related to life in arid habitats, and apply maximum likelihood methods to test if the origins of those traits temporally coincide with significant shifts in habitat, diversification rates and climatic changes. My results show that African lacertids experienced three major peaks in diversification, accompanied by the evolution of suites of arid-adapted morphological traits. These changes coincide with climatic shifts in Africa, including the transition from closed forests to open grasslands and savanna in the late Oligocene, prior to the peak temperatures of the mid-Miocene Climatic Optimum, and following the formation of the Benguela current leading to hyper-aridity in southern Africa. I conclude that deserts are important centers for reptile evolution, but that expected changes in climate due to global warming may outpace the ability of arid-dwelling species to adapt and persist in the future.

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While global variation in taxonomic diversity is strongly linked to latitude, the extent to which morphological disparity follows geographical gradients is less well known. We estimated patterns of lineage diversification, morphological disparity and rates of phenotypic evolution in the Old World lizard family Lacertidae, which displays a nearly inverse latitudinal diversity gradient with decreasing species richness towards the tropics. We found that lacertids exhibit relatively constant rates of lineage accumulation over time, although the majority of morphological variation appears to have originated during recent divergence events, resulting in increased partitioning of disparity within subclades. Among subclades, tropical arboreal taxa exhibited the fastest rates of shape change while temperate European taxa were the slowest, resulting in an inverse relationship between latitudinal diversity and rates of phenotypic evolution. This pattern demonstrates a compelling counterexample to the ecological opportunity theory of diversification, suggesting an uncoupling of the processes generating species diversity and morphological differentiation across spatial scales.

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The lizard fauna of Togo, a country situated within a natural gap in the rainforest zone of West Africa, is reviewed and updated. In this article, we summarize all available data on the distribution, ecology, and conservation status of the 43 lizard species of Togo. Species richness is uneven between vegetation zones. The submontane forest (ecological zone IV), despite being the smallest, houses the greatest number of species (n = 27), followed by dry forest (ecological zone II, n = 21). Currently none of the Togolese lizard species appears to be immediately threatened. However, several species are subjected to exploitation for the international pet trade and in-country use (bush-meat, fetish market), and could become threatened in the next decades. The intensity of this trade should be carefully monitored in the years to come.

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The dangers of helminth infestations for lizards, particularly infestations with nematodes und cestodes, are reported. Infection routes, diagnoses, und treatments are described.

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Report on keeping and breeding of the Green Keel-bellied Lizard (Gastropholis prasina).

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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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This paper presents the composition of the lizard fauna of Maringa-Lopori-Wamba landscape in the western portion of the central Congo basin in the Democratic Republic of the Congo and its weak similarity with the lizard fauna of Gaboon and Ituri faunal areas. It also fills a gap of knowledge in a region where no previous research on Sauria has been undertaken and signals the presence of Leptosiaphos hylophilus and Lygodactylus n. sp. The paper mentions the finding of a subspecies of Gastropholis echinata. These data are important since collected for the first time in a spot where no herpetological research on lizards has previously been undertaken.

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The Shimba Hills ecosystem along the south coast of Kenya is a key East African biodiversity hotspot. Historically, it is biogeographically assignable to the East African coastal biome. We examined the current Shimba Hills herpetofauna and their zoogeographical affinities to the coastal forests and nearby Eastern Arc Mountains biodiversity hotspots. The key studied sites included the Shimba Hills National Reserve, forest reserves, Kaya forests, and adjacent private land. Data on herpetofaunal richness were obtained from recent field surveys, literature, and specimens held at the National Museums of Kenya, Herpetology Section Collection, Nairobi. The Makadara, Mwele, and Longo- Mwagandi forests within the Shimba Hills National Reserve hosted the highest number of unique and rare species. Generally, the forest reserves and Kaya forests were important refuges for forestassociated species. On private land, Mukurumudzi Dam riparian areas were the best amphibian habitat and were host to three IUCN (Red List) Endangered- EN amphibian species, namely, Boulengerula changamwensis, Hyperolius rubrovermiculatus, and Afrixalus sylvaticus, as well as one snake species Elapsoidea nigra. Using herpetofauna as zoogeographic indicators, the Shimba Hills were determined to be at a crossroads between the coastal forests (13 endemic species) and the Eastern Arc Mountains (seven endemic species). Most of the Eastern Arc Mountains endemic species were from recent records, and thus more are likely to be found in the future. This ‘hybrid’ species richness pattern is attributable to the hilly topography of the Shimba Hills and their proximity to the Indian Ocean. This has contributed to the Shimba Hills being the richest herpetofauna area in Kenya, with a total of 89 and 36 reptile and amphibian species, respectively. Because of its unique zoogeography, the Shimba Hills ecosystem is undoubtedly a key biodiversity area for conservation investment.

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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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We provide an updated, commented list of the reptiles of Gabon, with their occurrence in the country’s protected areas, national parks and reserves. This list is part of a book describing the current status of knowledge of the biodiversity of Gabon, including detailed descriptions and abundant illustrations of its ecosystems and protected areas.

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We present new Gabonese locality records, ecological data or unpublished museum material for Crocodylus niloticus (Crocodylidae), Trionyx triunguis (Trionychidae), Agama lebretoni (Agamidae), Hemidactylus fasciatus and H. mabouia (Gekkonidae), Gastropholis echinata (Lacertidae), Trachylepis albilabris (Scincidae), Afrotyphlops angolensis (Typhlopidae), Dipsadoboa viridis, Hapsidophrys smaragdinus, Toxicodryas pulverulenta (Colubridae), Naja melanoleuca (Elapidae), Lamprophis olivaceus, Psammophis cf. phillipsii (Lamprophiidae), Natriciteres fuliginoides (Natricidae), Causus lichtensteinii and C. maculatus (Viperidae). We document predation cases by Hapsidophrys smaragdinus on Hemidactylus mabouia and Trachylepis albilabris, by Naja melanoleuca on Sclerophrys regularis (Anura: Bufonidae) and by Psammophis cf. phillipsii on Phrynobatrachus auritus (Anura: Phrynobatrachidae), and consumption of Arius latiscutatus (Siluriformes: Ariidae) and Tragelaphus spekii (Cetartiodactyla: Bovidae) by Crocodylus niloticus. We add one, two and one snake species, respectively, to Estuaire, Moyen-Ogooué and Nyanga provinces’ reptile lists. We add four reptile species to the list for Wonga-Wongué Presidential Reserve. We refer all records of Agama agama in Gabon to A. picticauda.

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The book ``Reptiles du Gabon`` provides an extensive description of the reptile fauna currently recorded from Gabon. It includes 122 species, among them 13 chelonians, 3 crocodiles, 32 lacertilians, 3 amphisbaenians and 70 snakes. Photographs, morphological diagnosis, natural history data and a map are given for each species, including a so far undescribed Lygodactylus from Ivindo National Park. Several herpetologists were invited to write chapters: E. Nicholas Arnold (introduction to Lacertidae), Mark Auliya (intro. to Pythonidae), Aaron M. Bauer (intro. to Gekkonidae), Wolfgang Bohme (intro. to Chamaeleonidae and Varanidae), Roger Bour (intro. to Pelomedusidae), Bill Branch (intro. to Cordylidae, Atractaspidinae and Elapidae), Donald G. Broadley (intro. to Amphisbaenidae), Jean-Philippe Chippaux (snake bites and first aid), Patrick David (intro. to Natricidae and Viperidae), Cornelius C. de Haan (intro. to Psammophiinae), Richard Fergusson (intro. to crocodiles), Jacques Fretey (intro. to sea turtles), Dieter Gramentz (intro. to Trionychidae), Danny Meirte (identification key to Colubridae, Lamprophiidae and Natricidae), Zoltan Tamas Nagy and Nicolas Vidal (intro. to systematics of African Caenophidia), Brice P. Noonan (intro. to Boidae), Richard Oslisly (reptiles in Gabon prehistoric rock art), Jarmo Perala (intro. to Testudinidae), Michel Raynal (Mokele-mbembe Brontosaurus-like cryptid), Andreas Schmitz (intro. to Scincidae), Philipp Wagner (intro. to Agamidae) and Van Wallach (intro. to Leptotyphlopidae and Typhlopidae). An extensive bibliography of Gabonese herpetology is given.

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Many animals display complex colour patterns that comprise several adjacent, often contrasting colour patches. Combining patches of complementary colours increases the overall conspicuousness of the complex pattern, enhancing signal detection. Therefore, selection for conspicuousness may act not only on the design of single colour patches, but also on their combination. Contrasting long- and short-wavelength colour patches are located on the ventral and lateral surfaces of many lacertid lizards. As the combination of long- and short-wavelength-based colours generates local chromatic contrast, we hypothesized that selection may favour the co-occurrence of lateral and ventral contrasting patches, resulting in complex colour patterns that maximize the overall conspicuousness of the signal. To test this hypothesis we performed a comparative phylogenetic study using a categorical colour classification based on spectral data and descriptive information on lacertid coloration collected from the literature. Our results demonstrate that conspicuous ventral (long wavelength-based) and lateral (short wavelength-based) colour patches co-occur throughout the lacertid phylogeny more often than expected by chance, especially in the subfamily Lacertini. These results suggest that selection promotes the evolution of the complex pattern rather than the acquisition of a single conspicuous colour patch, possibly due to the increased conspicuousness caused by the combination of colours with contrasting spectral properties.

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The herpetofauna of southern Africa is currently receiving an increased amount of attention. The Zoological Society of Southern Africa held a symposium on herpetology and ichthyology in 1975, the proceedings of which have been published in Zoologica Africana, and no less than 17 papers dealt specifically with research carried out recently on southern African amphibians and reptiles. Our aim in this chapter, therefore, can be no more than to sketch the present state of knowledge and thinking in a rapidly changing field.

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In July 1995 one specimen of Gastropholis echinata was collected near Fresco in southern Ivory Coast. The habitat consists of Oil Palm Farms. This is unusual because Gastropholis echinata is normaly dedicated to the canopy fauna of rain forests.

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While the stability of sex chromosomes is widely accepted in viviparous mammals and birds, ectothermic vertebrates are still largely viewed as having frequent turnovers in sex determining systems. Frequent changes in sex determining systems in ectotherms could be problematic for field ecological studies as well as for breeding programs, as molecular sexing across a phylogenetically widespread spectrum of ectothermic vertebrates would not be possible. However, we recently documented that sex determining systems in three important reptile lineages (caenophidian snakes, iguanas, and lacertid lizards) are in fact highly conserved. 2.We applied a new molecular procedure to identify sex within each of these three lineages (encompassing altogether around 4,000 species, i.e. nearly 50% of the recent species of reptiles). This technique uses quantitative PCR (qPCR) to compare copy numbers of genes specific for their respective Z (in caenophidian snakes and lacertids) and X (in iguanas) chromosomes between male and female genomes. The DNA samples required can be collected relatively non-invasively. Unlike molecular sexing based on repetitive elements, this technique can be easily applied to previously unstudied species of these lineages, as the number of copies of protein coding genes linked to the differentiated sex chromosomes is evolutionary highly conserved in each. 3.We suggest that qPCR-based molecular sexing using the comparison of gene copy number is a practical choice for non-model species of caenophidian snakes, iguanas and lacertids. Morever, it should also soon be available for other reptile lineages with differentiated sex chromosomes.

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Includes bibliographical references and index. Introduction. List of localities. New genus. List of new species and type localities. Preliminary note on the distribution of African lizards. Note on the distribution of African turtles -- Testudinata. Testudinae. Kinixys Bell. Pelomedusidae. Pelusios Wagler. Pelomedusa Wagler -- Loricata (Crocodilia). Crocodylidae. Crocodylus Laurenti. Osteoblepharon, new genus. Ecological notes on Congo crocodiles -- Squamata. Lacertilia. Geckonidae. Gonatodes Fitzinger. Hemidactylus Cuvier. Lygodactylus Gray. Agamidae. Agama Daudin. Varanidae. Varanus Merrem. Lacertidae. Lacerta Linnaeus. Bedriagaia Boulenger. Algiroides Fitzinger. Ichnotropis Peters. Eremias Wiegmann. Holaspis Gray. Gerrhosauridae. Gerrhosaurus Wiegmann. Scincidae. Mabuya Fitzinger. Lygosoma Gray. Ablepharus Fitzinger. Anelytropidae. Feylinia Gray. Chamaeleontidae. Chamaeleon Gronovius. Rhampholeon Günther -- Appendix A: Lists of the turtles, crocodiles, lizards, and chameleons of the rain forest and of the Sudanese subprovince -- Appendix B: Notes on the types of Hallowell`s West African species in the Academy of Natural Sciences of Philadelphia.

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This checklist records the 99 species of lizards known at present from Kenya, and which are divided amongst eight families: Gekkonidae 33 species, Agamidae seven, Chamaeleonidae 17, Scincidae 22, Lacertidae 12, Cordylidae five, Varanidae two, Amphisbaenidae one. Brief data on the distribution of all species is given, with some localities, details of habitat and (in some cases) status of subspecies. Some taxonomic notes on certain problematic species/genera are included, plus a brief discussion of the zoogeography of Kenya`s lizards, and a gazetteer of localities.

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The staggering phenotypic variation among organisms and the striking fit between an organism`s morphology and its environment have fascinated naturalists for centuries. Darwin`s publication of `On the origin of species` was the first to offer an explanation for the apparently perfect form-function relationship. During the past century overly enthousiastic evolutionary biologists interpreted any direct link between an organism`s morphology and ecology as evidence for the theory of evolution by natural selection. However, for morphological variation to be considered adaptive it is necessary to explicitly test how this variation translates into the variation in ecologically relevant performance traits, which in turn translates into ecological (and fitness) variation. Nowadays, performance- based ecomorphological approaches are typically used to test the adaptive nature of phenotypic variation in order to provide a better understanding of the selective pressures operating on organisms. Using an ecomorphological approach, lacertid lizards have been used extensively to test whether and how they are adapted to their environment. The majority of these studies have mainly included European species, leaving African species underrepresented. This is suprising from an evolutionary viewpoint. Compared to European lacertids, African lacertid lizard clades are older and more speciose. Also, lacertid lizard communities on the African continent are more complex than the ones in Europe (i.e. comprising 7-8 species versus 2-3 species). In this talk, we will focus on the phenotypic divergence among African clades and the link with the variation in performance and ecology, and explicitly compare these results to results on European lacertids.

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The amphibians and reptiles of Kibale National Park in western Uganda were inventoried over an 18-mo period in 1995 and 1996-97. A total of 75 species, including 28 amphibians and 47 reptiles, were collected or observed. Comparison with other equatorial African herpetofaunas confirms that the Kibale fauna is most similar to those of southwest Uganda and eastern Congo-Zaire, both hypothesized Pleistocene forest refugia. Comparison with a West Africa fauna also shows a fair degree of overlap, while almost no overlap was observed between Kibale and the forests of coastal East Africa. This confirms that the Kibale herpetofauna is an extension of the Guinea-Congolean forest faunas. Randomly placed 5 x 5 m plots were used to sample the herpetofauna of the forest leaflitter layer in unlogged forest, logged forest, and a neighboring exotic pine plantation. A total of 18 amphibian and reptile species were captured in the litter, a number similar to that observed in mid-elevation tropical forests in Central America and Southeast Asia. Density at Kibale was much lower than most previous studies. Analysis of the feeding ecology of the most abundant litter species showed that most diurnal litter frogs are active foragers of hard-bodied prey such as ants; sit-and-wait predators of larger soft-bodied prey are curiously absent. Plots sampled under fruiting Ficus natalensis trees showed significantly higher prey densities, but litter amphibians and reptiles did not seem to respond to this increase. Of the physical and biotic factors measured in each plot, seasonal changes in soil moisture were most closely correlated with the patterns of herpetofauna abundance observed in the forest. This is consistent with the fact that Kibale receives less rain than any site where the ecology of the litter herpetofauna has been studied, and that most of the species present in Kibale are believed to have evolved in the wetter forests of eastern Congo-Zaire.