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We measured the effects of deltamethrin, a pyrethroid insecticide, on individuals of two lizard species,Meroles suborbitalis and Pedioplanis namaquensis, in enclosures under controlled conditions, and under field conditions. We found significant effects on lizard mortality rates in the enclosure experiments, with most lizards dying within two months of treatment. Our field-based investigation, conducted over a five-month period, revealed significant reductions in abundance of M. suborbitalis (reduced by 52%) and P. namaquensis, (reduced by 72%) one and four weeks after spraying with deltamethrin. At 18 weeks after spraying there was no longer a significant difference in abundance measures between treatment and control plots, due to the invasion of the plots by juveniles.

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

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Estimates of phylogeny may allow historical events to be reconstructed even without a fossil record. The reliability of such interpretations depends not only on the robustness of the phylogeny but also on its topology. Changes in individual features can be traced and general histories of groups developed and compared with each other. Results are ofter surprising, for Instance the sophisticated tail shedding mechanism of lizards turns out to be a primitive feature that has been lost many times. Similarly, ecological analogues may have developed their common characaters in quite different orders. Phylogenies also provide a way of recognizing constraints and the effects of history on present ecological and behavioural patterns. When using anatomical characters the quality of the apparent phylogenies produced may be related to ecological history: expansion of a group along an ecological continuum into increasingly demanding niches ina small geographical area tends to produce a robust phylogeny (for instance in Meroles), while this is often not so for widely distributed groups that occupy a more modest range of niches (such as Pedioplanis and Podarcis). Non-morphological data may not show this tendency, but can have their own problems. Lacertids can be referred to clade with many successive branches in Africa and the Saharo-Eurasian arid zones and a less resolved probably paraphyletic complex of more primitive forms in the Mediterranean and wider Palaearctic areas. The African-Eurasian clade shows a general trend towards ground-dwelling and increasingly arid habitats but is ecologically variied. These animals are important to the study of Mediterranean forms because they provide eco-morphological parallels to them (for instance to Algyroides, Psammodromus and the archaeolacertas) and help form a basis for testing hypotheses about function. Although it is possible to recognise a number of distinct clades among the Mediterranean and Eurasian forms, relationships within and between these are often much less well substantiated. If results are available in time, current work on mitochondrial DNA sequencing will be discussed.

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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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New and additional distribution records are given for 12 amphibian, 25 lizard, one amphisbaenian, and five snake taxa from the Cape Province, South Africa. Some of the new records represent large range extensions, whereas others fill in gaps or confirm the occurrence of taxa in the region.

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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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A checklist of the lizards of the Cape Province, South Africa is presented. A total of 143 species and subspecies is recognized. The taxonomic status of no less than 84 (59,1%) of these has changed since the last review of the Cape lizards by FitzSimons (1943). Comments on the distribution and taxonomic status of problematic groups are included.

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Numerous new distribution records are given for 19 amphibian, 3 tortoise, 32 lizard, and 15 snake species and subspecies in the Cape Province, particularly in the eastern and central karroid regions. Many species are shown to have much wider distributions than previously believed. The importance of the mountains of the inland escarpment as a refugium for temperate species, the presence of isolated populations of western arid species in the karroid valleys of the northern Cape Fold Mountains, and the possible vicariant effects caused by sea level fluctuations on species inhabiting the southern Cape coastal plain, are briefly discussed.

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

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We discuss three aspects of the thermal biology of lacertid lizards. First, we provide an overview of the available data on field body temperatures (Tb), the thermal sensitivity of various performance functions and selected body temperatures in different species of lacertid lizards. We also briefly summarise information on the mechanisms of thermoregulation. Second, we discuss recent developments to estimate the »precision« of thermoregulation, and the contribution of distinct behavioural mechanisms. Finally, we revise available evidence for the existence of evolutionary adjustments of thermal characteristics in lacertid lizards. Existing studies have mainly dealt with within- and among-species differences in thermoregulatory behaviour (selected temperatures) and thermal physiology of adults (optimal temperatures, heating rates). Available data provide only limited evidence for clear-cut evolutionary shifts in thermal physiology characteristics along climatic gradients.

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Most lacertids are active foragers, but intrafamilial variation in foraging mode is greater than in most lizard families. We collected data on eight species of African lacertids to assess this variation. Both active and ambush foraging occurred within Pedioplanis and Meroles. Meroles ctenodactylus had a proportion of time moving and proportion of attacked prey detected while moving intermediate to those for actively foraging and ambushing Pedioplanis, but its number of movements per minute was exceptionally high. This species has a unique mixed foraging mode. Like active foragers, it seeks food by tongue-flicking while moving and spends a high percentage of the time moving. Like ambush foragers, it searches visually for prey during pauses between movements. Our findings confirm published data on four Kalahari lacertids. We discuss the history of foraging modes in advanced lacertids.

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Comparative analyses were carried out about the variability of the pileal shields of different species belonging to the family Lacertidae. The results of the comparisons have been evaluated in respect to the phylogenetical relationships existing between the different genera and species of the family.

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The phenotype of an individual has often been used as the descriminating factor in distinguishing species. However, with the advent of more precise molecular techniques, the genotype of species is increasingly being used as the preferred method in taxonomic classifications. Many taxa have recently been demonstrated to be incongruent in terms of their genetic and morphological groupings, and this may due to the influence that the environment may have on the morphological and functional aspects of a species. Selective pressures often act upon the performance of a species within a particular habitat first, and then selection for the morphological characters that allow for optimal performance occurs. Should genetically disparate species inhabit a particular environment, convergence in morphologies and performance may evolve. Historically, lizard species descriptions were based primarily on external morphologies, and thus misclassfication of species may have occurred due to mistakenly grouping species with convergent morphologies together. In the current dissertation, the links between morphology, performance capacities, diet and behaviour is explored in comparison to the environment and genetic relationships of southern African lacertid lizards. The performance capacities and associated morphological traits were expected to be more closely linked with the environment, and not closely linked with genetic relationships. To investigate these expectations, a multidisciplinary approach was taken, and genetic, morphological and performance analyses were done and compared with dietary behavioural and environmental analyses. In the first chapter, the link between habitat openness and the lizard bauplans is investigated and the presence of convergent morphologies within this group of lizards is uncovered. These convergences are shown to have resulted in misclassification of two lacertid species, and taxonomic revisions within the family are discussed. The second chapter explores the link between performance and associated morphological traits, and the dietary composition of the members of the Nucras genus. The third chapter identifies the link between the predator escape strategies employed by the members of the Meroles genus, and their morphologies and performance capacities. The fourth chapter explores the intraspecific, inter-population differences in morphologies and investigates the link between the morphological groupings and the population genetic groupings within Pedioplanis lineoocellata. The final chapter identifies whether adaptation to a novel habitat can occur over a relatively short period of time, and the morphological traits, functional aspects, and population genetic structure is investigated in conjunction with environmental analyses of vegetation and substrate between the populations of Meroles knoxii. It was concluded that the morphological and functional aspects of the southern African lacertid lizards are more closely related to the environment, particularly the microhabitat structure, than to their genetic relationships, and that future work using this group of lizards should involve a multidisplinary approach as different selective pressures are playing a role in shaping the morphologies and performance capacities of these lizards, compared to those that are acting upon the genotypes of the lizards.

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Survival, in part, depends on an individual`s ability to evade predators. In desert regions some lizard species have evolved head-first sand-diving strategies to escape predators. To facilitate this behaviour, a distinctive head morphology that facilitates sand-diving has evolved. This specialised head morphology may, however, come at a cost to other ecologically relevant functions, particularly bite force. Here, we investigated the relationship between morphology and function in a southern African lacertid lizard genus, Meroles, which consists of eight species that utilise different escape strategies, including sand-diving and running for cover. It was hypothesized that the specialised head morphology of diving species would negatively affect bite force capacity. We found that species from each escape strategy category differed significantly in head shape, but not bite force performance. A phylogenetic tree of the genus was constructed using two mitochondrial and two nuclear genes, and we conducted phylogenetic comparative analyses. One aspect of the head shape differed between the escape strategies once phylogeny was taken into account. We found that bite force may have co-evolved with head morphology, but that there was no trade-off between biting capacity and escape strategy in Meroles.

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Eremiadinae, one of three subfamilies of Lacertidae, are distributed throughout Asia and Africa. Previous phylogenetic studies suggested that one of the main groups of Eremiadinae (the Ethiopian clade) consist of two clades with predominately East-African and South-African distribution. Yet, especially the latter one, which includes the genera Pedioplanis, Meroles, Ichnotropis, Tropidosaura and Australolacerta, was not well supported in the molecular phylogenetic analysis. In this study, we analysed the phylogenetic relationships among the genera of the ‘South African clade’ to assess whether this group actually forms a highly supported clade and to address questions concerning the monophyly of the genera. We sequenced sections of the widely used mitochondrial genes coding for 16S rRNA, 12S rRNA and cytochrome b (altogether 2045 bp) as well as the nuclear genes c-mos, RAG-1, PRLR, KIF24, EXPH5 and RAG-2 (altogether 4473 bp). The combined data set increased the support values for several nodes considerably. Yet, the relationships among five major lineages within the ‘South African clade’ are not clearly resolved even with this large data set. We interpret this as a ‘hard polytomy’ due to fast radiation within the South African lacertids. The combined tree based on nine marker genes provides strong support for the ‘South African Clade’ and its sister group relationship with the ‘East African Clade’. Our results confirm the genus Tropidosaura as a monophylum, while Ichnotropis is paraphyletic in our trees: Ichnotropis squamulosa appears more closely related to Meroles than to Ichnotropis capensis. Furthermore, the monophyly of Meroles is questionable as well. Based on our results, I. squamulosa should be transferred from Ichnotropis into the genus Meroles. Also, the two species of Australolacerta (A. australis and A. rupicola) are very distantly related and the genus is perhaps paraphyletic, too. Finally we propose a phylogeographical scenario in the context of palaeoclimatic data and compare it with a previously postulated hypothesis.

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The reproductive cycle of the spotted sand lizard, Meroles suborbitalis was studied from a histological examination of gonads. The reproductive cycle is prolonged with males undergoing spermiogenesis in all months examined. Females with reproductively active ovaries were found in all months except July. Histological evidence is presented (corpora lutea and yolk deposition in the same ovary) that more than one clutch can be produced in the same reproductive period. Females undergo a quiescent period between clutches. Regression analysis revealed a significant correlation between female body size and clutch size. Mean clutch size for 55 gravid females was 3.98 [+ or -] 1.01 SD, range 1-6. One and two eggs are new minimum clutch sizes for M. suborbitalis. The smallest reproductively active male measured 45 mm SVL; the smallest reproductively active female measured 48 mm SVL. The prolonged reproductive cycle of M. suborbitalis resembles that of Meroles anchietae.

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An annotated checklist of indigenous and potentially indigenous Namibian terrestrial, aquatic and marine reptiles is presented. The purpose is to serve as an interim description of Namibian reptile diversity, to establish a taxonomic and biogeographical baseline, and as a preliminary review of the conservation status of Namibian reptiles. Two hundred and forty species of indigenous reptiles are presently known to occur in Namibia. These species comprise an array of approximately 265 described (but not always recognized) taxa, several of which are probably unwarranted. Species accounts are presented for all these species. Four accounts are for new species currently being described. Nineteen species have not yet been recorded from Namibia, but are expected to (accounts given) and another 6 species are less likely to occur (no accounts given). Full accounts are given for the 17 species which have been formally recorded in the past, but the lack of recent evidence suggests that the species is now locally extinct, the original report erroneous, or the species’ occurred as vagrants. Four additional species had been included on various published lists in the past, but have never been formally documented, no specimens are known to exist, and it is unlikely that the species would occur today even as vagrants (no accounts given). In total, 276 species-accounts are presented. Each account cites the original reference and type locality for each taxon, and a short description of the Namibian distribution. Emphasis is placed on Namibian and international legal and conservation status. Eighty-five species (33%) were found to be of local conservation concern. Gaps in knowledge (e.g. taxonomy, biogeography, and conservation status), where future research should be directed, are noted.

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The herpetofauna of the southern Kalahari has mixed affinities, as this area lies on a rainfall gradient in a critical area where a transition between the arid south-west and the moister north-east takes place. As the variation in substrate type is relatively limited, the effect of the rainfall gradient appears to influence and determine the range limits of many taxa in both directions, resulting in an area in which of 55 recorded reptiles, 11 western taxa overlap or form a parapatric zone with 25 eastern taxa, while the remaining taxa are endemic or wideranging.

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Data derived from the morphology of the seven species of South African sand lizards, Meroles (Reptilia, Lacertidae), and their outgroups produce a robust estimate of phylogeny when a maximum parsimony approach is applied. The estimate is fully resolved with little character conflict and internal branches are relatively long. This analysis indicates that Meroles is a true clade that includes the aberrant lacertid long separated as Aporosaura anchietae. The tree is pectinate, its successive external branches representing species with increasing adaptation to desert conditions, especially aeolian sand habitats. This pattern, and the robustness of the tree, support a model of invasion of severe habitats in which successive rounds of speciation, displacement, and adaptation result in spread into extreme ecological situations. To test the robust morphological phylogeny and, indirectly, the model as well, DNA from mitochondrial 12S and 16S ribosomal genes was sequenced and analyzed by both maximum parsimony and maximum likelihood approaches. Trees produced were largely congruent with that derived from morphology, although different from ones resulting from protein electrophoresis. However, in contrast to the internal branches of the morphological tree, those of the DNA maximum likelihood tree are quite short. The DNA data provide some corroboration for the relationships within Meroles based on morphology and consequently for the model as well. The disparity in internal branch lengths between the maximum parsimony morphological and maximum likelihood DNA trees may well indicate that the multiple adaptations to desert conditions arising on the main lineage of Meroles evolved quite rapidly. In this study DNA thus not only corroborates the phylogeny but also provides evidence about another aspect of evolutionary history.

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Namibia is mostly an arid and semi-arid country with a high number of reptile and fewer amphibian species. We review the herpetological literature dealing with Namibian species over the past fifty years, and provide up-to-date amphibian and reptile accounts using a widely accepted taxonomy and nomenclature. We critically discuss species accounts, draw attention to the historical development of species inventories for the country, and indicate species endemism for Namibia and the Namib Desert. In Namibia, the lizard families Gekkonidae, Lacertidae, and Scincidae have undergone adaptive radiations and are species-rich. This also applies to the snake family Psammophiidae. Areas of herpetological research that have received most attention are systematics (with its disciplines faunistics (area inventories), taxonomy, and phylogeny), ecology, and physiology. The former is indicative of early stages of herpetological research such as area inventories and the subsequent analyzes of the collections. The latter two were largely enabled by (1) species highly adapted to life in the hyper-arid Namib Desert, and (2) by the accessibility of these species in the Namib Desert through the infrastructure provided by the Gobabeb Research and Training Center. The majority of the eco-physiological research has focused on three highly psammophilus, diurnal lizard species; Meroles anchietae, M. cuneirostris, and Gerrhosaurus skoogi, whilst diverse geckos form the basis of eco-morphological studies. The concentration of research localities around cities and the Gobabeb Research and Training Center is characteristic for opportunistic research. Geographic centers of herpetological research have been the central Namib Desert (i.e. Gobabeb), and areas around Swakopmund and Windhoek. Extensive parts of Namibia remain barely touched. Herpetological publication frequency has been approximately the same since its beginning in the early 1800`s until the 1970`s. The period between 1986 and 2003 experienced a remarkable increase of publication activity that has slightly subsided around 2004 and picked up again in recent years. Recent conservation related studies investigate the impact of overgrazing with land degradation and water related issues such as canals and hydroelectric dam projects on herpetological communities. In the near future the impact of mining, especially Uranium mining in the Namib Desert, and the effects of climate change with the predicted drying and warming will demand increased attention. Advances in biotechnology with ever-increasing amounts of data and decreasing cost have and will progressively enable advances in traditional disciplines like taxonomy, phylogeny, and systematics. Additionally, these technologies will increasingly empower the newer disciplines of molecular ecology and conservation biology in Namibia. Annotated, updated species checklists highlight Namibian and Namib diversity and endemicity, and also direct researchers to the numerous taxonomic problems that still confound full understanding of the region`s herpetofauna.

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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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Background: Although current molecular clock methods offer greater flexibility in modelling evolutionary events, calibration of the clock with dates from the fossil record is still problematic for many groups. Here we implement several new approaches in molecular dating to estimate the evolutionary ages of Lacertidae, an Old World family of lizards with a poor fossil record and uncertain phylogeny. Four different models of rate variation are tested in a new program for Bayesian phylogenetic analysis called TreeTime, based on a combination of mitochondrial and nuclear gene sequences. We incorporate paleontological uncertainty into divergence estimates by expressing multiple calibration dates as a range of probabilistic distributions. We also test the reliability of our proposed calibrations by exploring effects of individual priors on posterior estimates. Results: According to the most reliable model, as indicated by Bayes factor comparison, modern lacertids arose shortly after the K/T transition and entered Africa about 45 million years ago, with the majority of their African radiation occurring in the Eocene and Oligocene. Our findings indicate much earlier origins for these clades than previously reported, and we discuss our results in light of paleogeographic trends during the Cenozoic. Conclusion: This study represents the first attempt to estimate evolutionary ages of a specific group of reptiles exhibiting uncertain phylogenetic relationships, molecular rate variation and a poor fossil record. Our results emphasize the sensitivity of molecular divergence dates to fossil calibrations, and support the use of combined molecular data sets and multiple, well-spaced dates from the fossil record as minimum node constraints. The bioinformatics program used here, TreeTime, is publicly available, and we recommend its use for molecular dating of taxa faced with similar challenges.

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We discuss seasonal variation in thermoregulatory behavior and its consequences on body temperature for 12 species of diurnal lizards in the southern Kalahari semidesert of Africa and also evaluate several methods of attempting to document thermoregulatory behavior using a descriptive data base. Lizards vary time of activity among seasons, which limits the variation in ambient conditions actually experienced. Ground-dwelling lizards and probably arboreal lizards move nonrandomly with respect to sun and shade; thus the percentage of lizards in sun in inversely proportional to air temperature. Arboreal lizards shift to higher perches at midday in summer and to logs or ground in winter thus decreasing and increasing incident heat loads, respectively. Both juveniles and adults of 3 species, only juveniles of 2 species, and only adults in 1 species are active in winter: both adults and juveniles of 6 species brumate [= hibernate]. Mean body temperature (T`b) varies within days and among months and is positively correlated with corresponding mean air temperature (T`a) in almost all species. Nonetheless, correlation and regression analysis suggests that thermoregulatory behaviors reduce the impact of variations in ambient conditions on Kalahari lizards. The mean T`b of different species reflect evolutionary relationships. In summer, mean T`b is proportional to the percentage of lizards in sun and with the tendency of lizards to be active only in summer. Thus, lizards with inferred low optimal temperatures are active during more months of the year.

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Desert lizards are typically either widely foraging or sit-and-wait predators, and these foraging modes are correlated with major differences in ecology. Foraging mode is related to the type of prey eaten by lizards. Widely foraging lizards in the Kalahari desert, the Western Australian desert, and the North American desert generally eat more prey that are sedentary, unpredictably distributed, and clumped (e.g., termites) or that are large and inaccessible (inactive scorpions) than do sit-and-wait lizards. In contrast, sit-and-wait lizards eat more prey that are active. Foraging mode also appears to influence the types of predators that in turn eat the lizards. For example, a sit-and-wait snake eats predominately widely foraging lizards. Crossovers in foraging mode thus exist between trophic levels. Widely foraging lizards may also encounter predators more frequently, as suggested by analyses of relative tail lengths; but tail break frequencies are ambiguous. Daily maintenance energetic expenditures of widely foraging lizards appear to be about 1.3-1.5 times greater than those of sit-and-wait lizards in the same habitats, but gross food gains are about 1.3-2.1 times greater. Widely foraging species also have lower relative clutch volumes, apparently in response to enhanced risks of predation. Foraging mode within one species varies with changes in food availability. Physiology, morphology, and risk of predation might generally restrict the flexibility of foraging mode. Because foraging mode constrains numerous important aspects of ecology, any general model of foraging velocity must be complex.

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The performance of ectotherms integrated over time depends in part on the position and shape of the distribution of body temperatures (Tb) experienced during activity. For several complementary reasons, physiological ecologists have long expected that Tb distributions during activity should have a long left tail (left‐skewed), but only infrequently have they quantified the magnitude and direction of Tb skewness in nature. To evaluate whether left‐skewed Tb distributions are general for diurnal desert lizards, we compiled and analysed Tb (∑ = 9,023 temperatures) from our own prior studies of active desert lizards in three continents (25 species in Western Australia, 10 in the Kalahari Desert of Africa and 10 species in western North America). We gathered these data over several decades, using standardized techniques. Many species showed significantly left‐skewed Tb distributions, even when records were restricted to summer months. However, magnitudes of skewness were always small, such that mean Tb were never more than 1°C lower than median Tb. The significance of Tb skewness was sensitive to sample size, and power tests reinforced this sensitivity. The magnitude of skewness was not obviously related to phylogeny, desert, body size or median body temperature. Moreover, a formal phylogenetic analysis is inappropriate because geography and phylogeny are confounded (i.e. are highly collinear). Skewness might be limited if lizards pre‐warm inside retreats before emerging in the morning, emerge only when operative temperatures are high enough to speed warming to activity Tb, or if cold lizards are especially wary and difficult to spot or catch. Telemetry studies may help evaluate these possibilities.

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We discuss seasonal variation in thermoregulatory behavior and its consequences on body temperature for 12 species of diurnal lizards in the southern Kalahari semidesert of Africa and also evaluate several methods of attempting to document thermoregulatory behavior using a descriptive data base. Lizards vary time of activity among seasons, which limits the variation in ambient conditions actually experienced. Ground-dwelling lizards and probably arboreal lizards move nonrandomly with respect to sun and shade; thus the percentage of lizards in sun is inversely proportional to air temperature. Arboreal lizards shift to higher perches at midday in summer and to logs or ground in winter thus decreasing and increasing incident heat loads, respectively. Both juveniles and adults of 3 species, only juveniles of 2 species, and only adults in I species are active in winter: both adults and juveniles of 6 species brumate [= hibernate]. Mean body temperature (T,) varies within days and among months and is positively correlated with corresponding mean air temperature (T,) in almost all species. Nonetheless, correlation and regression analysis suggests that thermoregulatory behaviors reduce the impact of variations in ambient conditions on Kalahari lizards. The mean Tb of different species reflect evolutionary relationships. In summer, mean T i s proportional to the percentage of lizards in sun and with the tendency of lizards to be active only in summer. Thus, lizards with inferred low optimal temperatures are active during more months of the year.

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Reptiles are supposed to be relatively invulnerable to the ongoing rapid anthropogenic climate change as they are able to actively regulate their body temperature (Tb) through behaviour, tolerate high Tb and resist water loss. However, recent studies have shown that lizards and snakes seem to be more at risk than previously expected. In Mexico, increased local extinction probability in lizards correlated with the magnitude of warming during the reproductive period, questioning the assumption of climate invulnerability. We tested the hypothesis that different lizard species of the family Lacertidae are vulnerable to rises in maximum temperatures in Namibia, especially in the Namib and the Kalahari. We predicted that inhabiting different habitats with different microhabitat temperatures and different preferred Tb within different distribution ranges would result in differences in local extinction probability. As opposed to other studies our model integrates past and present distributions verified by museum collections and ground-truthed, a quantifiable physiological parameter (preferred body temperature Tpref) and available operative temperatures in correlation to air temperatures. Data was collected for 17 species (Meroles anchietae, M. cuneirostris, M. suborbitalis, M. ctenodactylus, M. reticulatus, M. micropholidotus, M. knoxii, Pedioplanis namaquensis, P. laticeps, P. lineoocellata, P. breviceps, P. rubens, P. undata, P. inornata, P. gaerdesi, P. husabensis and Heliobolus lugubris). Our first results seem to indicate that populations of at least one of the tested species were extirpated (both predicted by the model and verified) in the hottest area of its distribution range due to increased maximum temperatures during the reproductive season since the mid-1970s. Furthermore, different extents in future extinction risk are predicted under consideration of the currently accepted climate change scenarios. It seems that Namibian Lacertidae under current conditions already live at their thermal maximum.

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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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In both December 1992 and September 1995 I travelled through South Africa and Namibia. In the Daan Viljoen park in Windhoek Agama planiceps, Mabuya spilogaster and Pachydac- tylus bibroni were found. Pedioplanis brevi- ceps was seen in trees and bushes of the Namib Desert while in the barer valleys Pedioplanis undata undata was observed. A Chamaeleo namaquensis was seen in a small bush. Other species which were recorded were M. spilogaster and Ptenopus garrulus macula- Ius. In the Kalahari Gemsbokpark only M. spi- logaster, Agama aculeata aculeata and Pelomedusa subrufa were seen, the latter after a shower. Pedioplanis undata inomata, Mabuya sulcata, Mabuya variegata, Platysaurus capensis, Agama anchietae, Pedioplanis namaquensis, Cordylus po/yzonus and Pachydactylus bibroni were found in Fish River Canyon by the camp site. The tempera- ture can rise to 45°C over the day. The lizards seemed to go into shock when captured. In 1995 I spent a long time in Namaqualand. Here a lot of reptiles were found in a relative- ly small area. These included: Cordylus cataphractus, Cordylus polyzonus, Pediopla- nis lineocellata pulchella, Meroles suborbi- talis, Agama hispida hispida, Bitis arietans, Homopus signatus signatus and Chersina angulata. In the Mediterranean climatic zone and in the Karoo the following unusual species were recorded: Psammo- bates tentorius trimeni, Geochelone parda- lis and Pseudocordy/us capensis.

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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.

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13 species of the genera Aporosaura, Meroles, Pedioplanis, and Heliobolus horn Namibia and additionally Pedioplanis burcheUi from the Republic of South-Africa have been investigated proteinelectrophoretically concerning 14 genetic loci. Pedioplanis and Meroles turned out to be sister groups, Heliobolus and Aporosaura are standing further apart. The su bgenera of Meroles (Meroles s. str. and Saurites) could not be parted distinctly. The morphological correspondence between Aporosaura and Saurites has been interpreted as convergent adaptions to their habitat.

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The family Lacertidae encompasses more than 250 species distributed in the Palearctis, Ethiopis and Orientalis. Lacertids have been subjected in the past to several morphological and molecular studies to establish their phylogeny. However, the problems of convergent adaptation in morphology and of excessively variable molecular markers have hampered the establishment of well supported deeper phylogenetic relationships. Particularly the adaptations to xeric environments have often been used to establish a scenario for the origin and radiation of major lineages within lacertids. Here we present a molecular phylogenetic study based on two nuclear marker genes and representatives of 37 lacertid genera and distinct species groups (as in the case of the collective genus Lacerta). Roughly 1600 bp of the nuclear rag1 and c-mos genes were sequenced and analyzed. While the results provide good support to the hitherto suggested main subfamilies of Gallotiinae (Gallotia and Psammodromus), Eremiainae and Lacertinae [Harris, D.J., Arnold, E.N., Thomas, R.H., 1998. Relationships of lacertid lizards (Reptilia: Lacertidae) estimated from mitochondrial DNA sequences and morphology. Proc. R. Soc. Lond. B 265, 1939–1948], they also suggest unexpected relationships. In particular, the oriental genus Takydromus, previously considered the sister-group to the three subfamilies, is nested within Lacertinae. Moreover, the genera within the Eremiainae are further divided into two groups, roughly corresponding to their respective geographical distributions in the Ethiopian and the Saharo-Eurasian ranges. The results support an independent origin of adaptations to xeric conditions in different subfamilies. The relationships within the subfamily Lacertinae could not be resolved with the markers used. The species groups of the collective genus Lacerta show a bush-like topology in the inferred Bayesian tree, suggesting rapid radiation. The composition of the subfamilies Eremiainae and Lacertinae as well as their phylogeography are discussed.

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Die Wüstenrenner-Eidechsen Namibias werden derzeit in folgende vier Gattungen eingeteilt: Pedioplanis, Meroles, Aporosaura und Heliobolus. Während zweier Reisen konnten sie im Freiland studiert werden. Im Terrarium wurden sieben Arten gehalten, von denen vier Arten nachgezüchtet werden konnten. Neben Pedioplanis rubens, P. lineoocellata pulchella und P. namaquensis erweist sich vor allem Meroles cuneirostris als ein sehr gut zu haltendes, interessantes Terrarientier.

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Two hundred twenty-two individual reptiles (11 families, 45 species) from 17 districts of Namibia were examined for endoparasites. Thirty-three (31 lizards, 2 snakes) individuals (15%) were found to harbor at least 1 species of helminth; 4 lizards harbored a multiple infection of 2 helminths, 1 lizard was infected with 3 species, and 1 lizard harbored a multiple infection of 5 species. One species of linstowiid cestode, 12 species of nematodes representing 6 families, and 1 species of cephalobaenid pentastomid were found in the herpetofauna surveyed. Twenty-seven new host and 8 new geographic records are documented for helminths of Namibian reptiles.

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Lizards are a diverse clade in which one radiation consists entirely of sit-and-wait foragers and another consists of wide foragers. Lizards utilizing these two foraging modes are known to differ in diet, but little is known about how feeding morphology relates to diet and/or foraging mode. This study tested the hypothesis that skull morphology and biting performance are related to diet preference, and consequently, coevolve with foraging mode. Four species of lacertid lizard were studied because they vary in foraging mode, their phylogenetic relationships are known and they are well studied ecologically. Using an ‘ecomorphological’ approach, skull morphology and biting performance were quantified and mapped on to the phylogeny for the species. The results indicate that sit-and-wait species have shorter, wider skulls than the wide foraging species, and that all are significantly different in overall head shape. The sit-and-wait species had similar values for biting performance; however, clear phylogenetic patterns of covariation were not present between sit-and-wait and wide foraging species for either biting performance or skull morphology. Thus, skull morphology and performance have little influence on diet and foraging mode in these species. Instead it is likely that other factors such as seasonal prey availability and/or life history strategy shape foraging mode decisions.

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Foraging behaviors exist along a continuum from highly sedentary, ambush foraging, to more continuous searching, or active foraging. Foraging strategies, or modes, are defined based upon locomotor behaviors (e.g. percent time moving, moves per minute). In lizards, traits correlated with ambush and active foraging have been of interest for some time; however, general patterns of correlated evolution between locomotor morphology and locomotor behavior have only recently begun to be quantified. In this study, variation in hindlimb morphology is investigated in a model group of lizard species that vary between active foraging and more sedentary (or mixed) foraging mode. Canonical variates analysis reveals that the two active foraging species occupy similar regions of the morphospace, while the two more sedentary species occupy different regions. The active foraging species have a narrow pelvis with shorter tibia and femora. The more sedentary species have a wide pelvis, long tibia and femora, and slightly longer metatarsals. Phylogenetic patterns of trait variation were examined through ancestral character state reconstruction and show morphological shifts in concert with foraging mode in these species. The observed shifts in locomotor morphology are discussed in light of published data on sprint speed and endurance in these species. Together, the data show that linking morphological variation to variation in stride length and stride frequency is critical to understanding the evolution of locomotor performance. Much more stride length and frequency data are needed among ambush, mixed, and active foraging species because these parameters, and their morphological components, are likely correlated with variation in food acquisition mode.

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

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

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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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From 12 to 18 species of desert lizards occur in ecologic sympatry on 10 study areas in the Kalahari desert of southern Africa. The number of species of diurnal lizards is similar to the number in the North American deserts, while the nocturnal component of the saurofauna is more comparable to that occurring in the Australian deserts. The between-habitat component of species density is similar in the American and the Kalahari deserts, but is markedly greater in the Australian desert. A variety of climatic and vegetational statistics are examined for the 10 areas, and correlations with lizard species density are discussed.

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

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

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Evolutionary changes in foraging style are often believed to require concurrent changes in a complex suite of morphological, physiological, behavioural and life-history traits. In lizards, species from families with a predominantly sit-and-wait foraging style tend to be more stocky and robust, with larger heads and mouths than species belonging to actively foraging families. Here, we test whether morphology and foraging behaviour show similar patterns of association within the family Lacertidae. We also examine the association of bite force abilities with morphology and foraging behaviour. Lacertid lizards exhibit considerable interspecific variation in foraging indices, and we found some evidence for a covariation between foraging style and body shape. However, the observed relationships are not always in line with the predictions. Also, the significance of the relationships varies with the evolutionary model used. Our results challenge the idea that foraging style is evolutionarily conservative and invariably associated with particular morphologies. It appears that the flexibility of foraging mode and its morphological correlates varies among lizard taxa.