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The ability to shed (autotomize) all or part of the tail, usually in response to predator attack, and often to subsequently regenerate it is widespread in lizards and amphisbaenians and also occurs in a few snakes and in the tuatara. Most species possess a sophisticated intravertebral autotomy mechanism which seems to be primitive in the Squamata. This appears to have been independently lost in members of many groups, but some agamids and snakes have regained the ability to shed their tails by a simpler intervertebral means and a -number of agamids have also redeveloped tail regeneration as well. Breakable tails are used to evade capture in two main ways: by enabling reptiles to break away from predators that have grasped them by the tail and by providing a distraction which deflects the attention of the attacker away from the vulnerable head and body. It is argued that loss of caudal autotomy has occurred when the costs of tail shedding outweigh its benefits. Likely costs include the expense of regrowing the tail and the loss of a variety of possible tail functions that may cause partial incapacitation, at least until the tail regenerates. Benefits of autotomy are liable to be low if predation is rare, if the animal is able to protect itself effectively in other ways, if it is too slow to evade further pursuit after the tail is shed, or if the tail is small or unpalatable and consequently not likely to distract a predator. Benefit variation may well be greater than cost variation and therefore more important in initiating the loss of autotomy mechanisms. Many taxa that do not shed the tail appear to conform to the above interpretation, but in some cases, such as the Platynota, Agamidae and Chamaeleonidae, lack of intravertebral autotomy may reflect the history of these groups rather than being a direct result of present ecological pressures. The distribution of intervertebral autotomy in the Agamidae suggests that it may have evolved only in rather special circumstances where tail fragility is advantageous even in the absence of the ability to regenerate. Restriction ot autotomy planes to the tail-base, so that the whole organ is lost, a condition found in a number of relatively slow-moving geckoes, is interpreted as a means of ensuring that enough of the tail is shed to distract a predator from further pursuit. The stimulus necessary to induce autotomy can vary rapidly in individual lizards and at least some of these changes probably maximize the effectiveness of the tail-shedding mechanism. Differences in the readiness with which all or part of the tail is shed exist between species and are likely to reflect the balance of costs and benefits in particular cases. Variations in incidence of broken tails between species and populations may be due to such differences in fragility but many other factors may play a part, including the age structure of samples, incidence of unsuccessful attacks by predators and ability to evade predators after autotomy. There is a clear tendency for climbing lizards, especially those living on rock surfaces, to have higher incidences of broken tails than ground-dwelling species, perhaps because the tail is usually less important in locomotion in the first group. Many lizards possess conspicuously coloured tails and tail movements that seem likely to help distract attention from the head and body. Conspicuous tail colouring is more frequent and often better developed in young animals, which tend to be more vulnerable than adults, and in active species from open habitats where crypsis may not always be very effective. Conspicuous tails usually have contrasting light and dark areas in nocturnal forms but are often a single bright colour in diurnal ones, probably reflecting the visual capacities of their respective predators. The predominance of blue tails in day-active species may be because this colour is striking close to but not very arresting at a distance, so it may not attract predators from far away while still drawing their attention at close quarters.

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Twenty-four species of lacertid lizards were examined at 31 sites in western Yogoslavia, Greece and Iberia. Comparative observations were made on over 4500 individual lizards, noting such features as times of activitiy, hunting methods, diet, micro- and macrohabitat, refuges used and body temperature. These data are used as a basis for assessing resource partition in related sympatric species, for find out whether different systematic groups have characteristic types of niche, and for comparing cumminity structures in the peninsulas of southern Europa. Acanthodactylus erythrurus, Algyroides marchi, Algyroides moreoticus, Algyroides nigropunctatus, Lacerta agilis, Lacerta graeca, Lacerta horvathi, Lacerta lepida, Lacerta monticola, Lacerta oxycephala, Lacerta mosorensis, Lacerta schreiberi, Lacerta trilineata, Lacerta viridis, Lacerta vivipara, Podarcis bocagei, Podarcis erhardii, Podarcis hispanica, Podarcis melisellensis, Podarcis milensis, Podarcis muralis, Podarcis peloponnesiaca, Podarcis sicula, Podarcis taurica, Psammodromus algirus, Psammodromus hispanicus.

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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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DNA sequence indicates the Lacertidae contain two subfamilies, Gallotiinae and Lacertinae, the latter comprising two monophyletic tribes, the Eremiadini of Africa and arid southwest and central Asia, and the Lacertini of Europe, northwest Africa and southwest and east Asia. Relationships within the 108 species of Lacertini are explored using mtDNA (291 bp cytochrome b; 329 bp 12S rRNA for 59 nominal species, and reanalysis of the data of Harris et al. 1998, and Fu 2000). The morphology of the tribe is reviewed and 64 of its characters (equivalent to 83 binary ones) also used to assess relationships. The Lacertini are assigned to 19 monophyletic units of 1 to 27 species, recognised here as the following genera (contents are indicated in brackets): Algyroides, Anatololacerta gen. nov. (L. danfordi group), Apathya (L. cappadocica group), Archaeolacerta (L. bedriagae), Dalmatolacerta gen. nov. (L. oxycephala), Darevskia (L. saxicola group), Dinarolacerta gen. nov. (L. mosorensis), Hellenolacerta gen. nov. (L. graeca), Iberolacerta (L. monticola group), Iranolacerta gen. nov. (L. brandtii and L. zagrosica), Lacerta s. str. (sand and green lizards, L. agilis group), Parvilacerta gen. nov. (L. parva and L. fraasii), Phoenicolacerta gen. nov. (L. laevis group), Podarcis (wall lizards), Scelarcis (L. perspicillata), Takydromus (Asian grass lizards), Teira (L. dugesii), Timon (ocellated lizards, L. lepida group) and Zootoca (L. vivipara). Both mtDNA and morphology indicate that Lacerta and Timon are sister taxa, and DNA suggests further possible relationships among genera (Fig. 1, p. 6). Neither DNA nor morphology indicates that the archaeolacertas (sometimes formalised as Archaeolacerta sens. lat.) form a clade. Instead, they are representatives of an ecomorph associated with living on rock exposures and using the narrow crevices that these contain. The Lacertidae probably arose in the European area, with the Gallotiinae later reaching Northwest Africa and the Canary Islands, and the ancestor of the Eremiadini invading Africa in the mid-Miocene. The Lacertini spread through much of their present European range and diversified, perhaps largely by repeated vicariance, around 12–16 My ago, producing the ancestors of the present mainly small-bodied genera, which then underwent often modest speciation. Three units spread more widely: the Lacerta-Timon clade of large-bodied lizards probably dispersed earliest, followed by Algyroides and then Podarcis. Overall, European Lacertidae show a pattern of repeated spread, often accompanied by restriction of previous groups. Expansion of Lacertini may have displaced earlier lacertid lineages from all or much of Europe; while spread of Podarcis may have restricted many other genera of Lacertini. The earlier expansion of the Lacerta-Timon clade probably did not have this effect, as difference in adult body size restricted competitive interaction with other forms. Several invasions of more distant areas also occurred: of East Asia by Takydromus over 10 My ago, and more recently of northwest Africa by Podarcis, Scelarcis and Timon, and Madeira by Teira. Relationships within the Eremiadini estimated from both mtDNA, and nDNA differ considerably from those based on morphology. They indicate relatively mesic forms may have diversified widely across Africa and given rise to at least three independent invasions of arid habitats. MtDNA also indicates that Lacerta andreanskyi belongs in the Eremiadini and may occupy a basal position there. It is assigned to a further new genus, Atlantolacerta gen. nov.

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The microornamentation of the scales (oberhautchen) has been studied by means of enamel casts (in negative), or with detached skin pieces (positive cast in the upper face or negative in their lower face of the scales) and its observation by transparency with optical microscopy at 40x, 400x and 1000x. In this study we have found a remarkable uniformity in all genera of Lacertini studied (already known, although significantly expanding the number of species previously studied). In light of the results obtained, it seems that the use of the microornamentation of the scales in taxonomy is limited. There is a remarkable degree of variation and probably of homoplasy, as it happens in so many characters of Lacertini. Nor is it clearly linked to certain conditions of the environment, although it may have a certain importance in mechanisms such as evapotranspiration and perhaps in the crypsis through its influence on the reflectance of the scales. These scales can present protuberances (like small tubercles) on their surface (derived character) in Algyroides (the four species), and in the case of Algyroides marchi also seems to present small pits on its scale surface. In most lacertids the cells of the “oberhautchen” are usually narrow (or short anteroposteriorly, if preferred), between 1 and 4 μm, having the appearance of ribbons or transverse straps. Smaller sizes (derivated) appear more or less marked in Algyroides spp, Darevskia praticola complex, Parvilacerta spp and in Dinarolacerta mosorensis (although not in D. montenegrina) and is difficult to interpret. Except in Dinarolacerta, in the other species it coincides that they are ground or ground-rock interface species, and the coarser stripes could have to do with reflectance (imitating the vegetation or the medium between which they move, according to the hypothesis of Allam et al.). In the case of Dinarolacerta, very saxicolous, it is probably the sister group of Algyroides and the common morphology could have a phylogenetic origin linked to its relationship with Algyroides. There is also no relationship with moisture since some come from dry places and others are from very wet areas. The posterior flange of the cells may be slightly mounted in the next cell (primitive character) but appears quite raised (derived character) in Algyroides nigropunctatus (much less in A. moreoticus and A. marchi, and apparently little or nothing in A. fitzingeri). The rear flange of the cells can be smooth, corrugated or notched. In our samples, irregular (and even dentate) posterior ridges appear in numerous Darevskia such as D. derjugini, D. parvula, D. raddei complex [D. raddei raddei, D. r. vanensis and D. nairensis], in part of the group of D. rudis [D. rudis sspp. and D. bithynica sspp.], several Iberolacerta (I. bonnali, I. horvathi and I. monticola astur), as well as in Teira dugesii. The character appears, although less marked in Algyroides (more in A. moreoticus, but less marked or barely visible in the others), in Hellenolacerta graeca, and other Iberolacerta (I. aurelioi, I. martinezricai, and scarcely marked in I. cyreni). Very little marked in Darevskia mixta, somewhat more in D. dryada and none in D. clarkorum, and also appears in the group of D. saxicola (D. saxicola, D. brauneri brauneri, D. b. darevskii, D. lindholdmi, D. szczerbaki), Dalmatolacerta oxycephala, Dinarolacerta mosorensis (only in the Biokovo sample, and not in Durmitor or D. montenegrina), Apathya cappadocica, in some places of the scales of Parvilacerta fraasii (but not in P. parva) and very little in D. (p) hungarica; also in the remaining group of D. rudis (D. valentini valentini, D. v. lantzicyreni, D. rudis bolkardaghica, D. portschinskii), and some parthenogenetic species (D. armeniaca, D. dahli, D. rostombekowi) but not in D. unisexualis, D. uzzelli, D. sapphirina, D. bendimahiensis or in the triploid hybrid between D. unisexualis and D. nairensis. In these parthenogenetic species it seems a general rule that the character of the crenulation or irregularity of the posterior flange of the cells resembles that of the paternal rather than the maternal species. The exception is the triploid hybrid [arisen from the hybridization of D. unisexualis (parthenogenetic female, without the character) and a male of D. nairensis (with fairly developed character)] that lacks character, and in this case is more similar to the maternal species of which has two genetic sets compared to only one of the paternal one.

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In connectivity conservation and ecological network planning, the selection of focal fragmentationsensitive species represents a priority step. Nevertheless, despite their strategic role, selection of focal species has traditionally been carried out using charismatic and/or non objective approaches. In this way, actions of planning and conservation could be ineffective. Using as a case study Italian reptiles, we apply an expert-based approach for the selection of focal species on the basis of sensitivity to components of habitat fragmentation (habitat area reduction, increase of habitat isolation, increase of edge effect and landscape matrix disturbance) and of intrinsic ecological traits of the species (trophic level, dispersal ability, body size, niche breadth, rarity). The threshold values for each component of fragmentation defined a set of 21 focal species that can be divided into the three macro-components of human-induced habitat fragmentation (HIHF) towards which they show a sensitivity, the suitable spatial scale of populations and relative suitable habitat categories. Among these species, seven can be sampled easily with standard, low-cost field protocols. The selected species largely coincide with the species known in literature as fragmentation-sensitive.

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We report here results of a short-term study on field body temperatures and aspects of thermoregulatory behavior of the lizard Lacerta bedriagae . Field work was carried out from 31 May to 3 June 1988 near Haut-Asco (Corsica, France), where L. bedriagae seems to be restricted to altitudes > 1650 m. The study area was between 1750 and 1800 m elevation on the steep east-facing slope of Mont Mufrella.

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New data on the distribution of the herpetofauna of the La Maddalena Archipelago are reported in the present work, together with the available literature. The study reports data on 78 islands, for 19 of these islands the data are unpublished.

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Thermoregulation is essential for ectotherms but its relative cost, especially under ongoing climate change, depends on the thermal quality of habitats. Populations at the warm margin of a thermal niche could be negatively affected by environmental temperatures that approach the limits of a species’ thermoregulation capacity. This study aims to define the thermal niche of the Bedriaga’s rock lizard, Archaeolacerta bedriagae, a rock-dwelling species endemic to the Corsica and Sardinia islands (western Mediterranean Sea), and to investigate its thermoregulation effectiveness at the warm edge of its niche. We collected data on climate, body temperature, and microhabitat temperature throughout the species’ range to characterize its thermal niche. We found that A. bedriagae does not occupy the entire climatic space available across its distribution range; rather, it selects temperate climates. Remarkably, thermoregulation effort increases when the habitat thermal quality decreases towards warmer sites. Populations at the warm edge of the thermal niche show the best thermoregulation effectiveness, but they are also more sensitive to the effects of climate change as they may already be at (or beyond) the species’ maximum thermal capacity under the current conditions. We observed such a pattern at the extreme hot side of the thermal niche. This study provides key information on the thermoregulatory response of A. bedriagae to ongoing climate change that can be useful to identify populations facing a higher extinction risk either currently or in the near future.

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For planning practical measures aimed at biodiversity protection, conservation priorities must be identified at a local scale. Unfortunately, identifying local conservation priorities requires high-resolution data on species distribution, and these are often unavailable. Atlases of species distribution provide data for several groups of organisms in many different areas but are often too coarse in resolution to provide valuable information. We explored the possibility of cross-scale modelling species distributions and we clarified, for the first time, its effect on prioritization exercises. We used different modelling techniques for scaling down atlas data for Sardinian reptiles, validated the outcomes with detailed, field-sampled data, and compared conservation priorities deriving from atlas maps and downscaled models. Doing this, we obtained as a further result the identification of priority species and areas for future conservation strategies. Our results encourage us to experiment further with this approach. Through the downscaling procedure, we obtain high-resolution models with strong variations in predictive performances, although most of the models show satisfactory/excellent scores. This testifies that low-resolution data can be downscaled maintaining low rates of omission and commission errors. Increasing the resolution of distribution maps used for prioritization influences the spatial patterns of priority but does not modify the evaluation of species representation. Overall, we show that atlases can meet the large demand for distribution data by decision makers if appropriate downscaling procedures are adopted. In addition, we provide practical instruments for the conservation of reptiles in Sardinia by identifying priority species and areas that require strict management.

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Studies of the ecological characteristics of sympatric species are important for developing and testing ecological theory, but may be of interest also for conservation biology research when the study species are threatened, endemic and with narrow distribution. Here, we studied a particular aspect of the ecology (i.e. microhabitat use) of two sympatric lizards (Archaeolacerta bedriagae, Podarcis tiliguerta) endemic to Sardinia and Corsica (Tyrrhenian islands). We studied this issue by modelling procedures, using field data collected at six study areas in both Sardinia and Corsica. We recorded 18 microhabitat variables for each lizard spot. The variables were entered as independent variables in logistic regression analysis with the presence/absence data for the lizards as the dependent variable, and Akaike Information Criterion was applied to select the best models describing the ecological equation of each study species. In total, we based our modelling approach on 296 individuals of A. bedriagae and 182 of P. tiliguerta. The general logistic regression models revealed that five distinct variables were significantly correlated to the presence/absence of A. bedriagae, and six to that of P. tiliguerta. We found that three variables were important for only P. tiliguerta, two for only A. bedriagae, and three for both species and with an identical sign. We also found some similarities in microhabitat choice between species. Indeed, some variables were always present in the best models of both A. bedriagae and P. tiliguerta. In general, A. bedriagae was more related to spots with large stones and low vegetation than P. tiliguerta, which, on the contrary, choose spots relatively closer to vegetation. The various reasons explaining the observed similarities and differences between species were examined. It is suggested that our modelling procedure may be widely used for studies of lizard community ecology, because it easy to use and allows a more-in-depth analysis than normal `count approaches`.

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Many techniques for predicting species potential distribution were recently developed. Despite the international interest for these procedures, applications of predictive approaches to the study of Italian fauna distribution are exceptionally rare. This paper aimed at: (a) detecting climatic exigencies of A. bedriagae in Sardinia; (b) predicting the Archaeolacerta bedriagae Sardinian potential distribution; (c) identifying the most vulnerable Italian populations of the species. Literature and field data were utilized as presence records. Six modelling procedures (BIOCLIM, DOMAIN, ENFA, GAM, GLM, and MAXENT) were adopted. The species climatic requirements were defined using the WorldClim databank for deriving the environmental predictors. AUC and Kappa values were calculated for models validation. AUC values were compared by using Anova Monte Carlo. The best four models were combined through the weighted average consensus method for producing a univocal output. GAM and MAXENT had the best performances (respectively: AUC = 0.93 ± 0.03, Kappa = 0.77 ± 0.08; AUC = 0.93 ± 0.03, Kappa = 0.78 ± 0.07). Good results were also obtained by GLM and DOMAIN (respectively: AUC = 0.89 ± 0.04, Kappa = 0.72 ± 0.05; AUC = 0.88 ± 0.04, Kappa = 0.69 ± 0.07). BIOCLIM and ENFA gained relatively low performances (respectively: AUC = 0.78 ± 0.07, Kappa = 0.57 ± 0.14; AUC = 0.75 ± 0.06; Kappa = 0.49 ± 0.10). In Sardinia A. bedriagae is mainly influenced by seasonality, which causes the evidenced range fragmentation. Moreover, the general importance of multi-methods approaches and consensus techniques in predicting species distribution was highlighted.

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Arcbaeolacerta bedriagae is a polytypic species endemie to Corsica and Sardinia II represents one of the most peculiar elements of the Italian herpetofauna. This species has a fragmented range in Sardinia. The aim of this paper is to summarise the knowledge on the distribution of this lizard in Sardinia, based both on literature and original records, and to define the conservation status of its populations This research was carried out throughout the entire Sardinian territory, from June 2000 to September 2002. Most of the known sites of occurrence of A. bedriagae were checked, characterised from geomorphologic and florofaunistic points of view and gco-referenced. The surveys carried out explored only the potentially suitable habitats in different hours of the day. Three new localities were discovered, 10 checked sites were confirmed, 12 localities were not confirmed and 43 previously quoted sites were not explored. Two sampling sites were selected for a population study. In the latter two localities, several population parameters, such as density and sex ratio were studied. In the mountain site, a population density twenty limes higher than that found at the sea level site was estimated. Only five species were found to be syntopic with A. bedriagae, Podarcis tiliguerta, Algyroides fitzingeri, Tarentola mauritanica, Chalcides ocellatus and Coluber viridiflavus. The Sardinian subrange includes seven main areas of certain presence, but an underestimation due to their elusivity and the low density of some populations is possible The species generally inhabits areas of scarce interest and difficult for man to reach, though at least in some localities it seems to be disturbed by an increase in tourism. Some conservation actions were proposed.

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The author describes a herpetological vacation on Corsica. It is an island with lots ofdifferent habitats, where reptiles and amphibians are abundant. Several (sub)species are endemic to Corsica or to both Corsica and Sardinia, for instance Archaeolacerta bedriagae, Podarcis tiliguerta, Algyroides fitzingeri, Discoglossus montalemii, D. sardus, Hyla sarda, Euproctus montanus, Salamandra salamandra corsica and Natrix natrix corsa. Several others are probably introduced by men, for instance Podarcis sicula cam- pestris (in Ajaccio, Porro-Vecchio and Basria), P. s. cettii (in Bonifacio), Tarentola mauritanica, Rana esculenta, Bufo viridis and Testudo hermanni. Corsica and Sardinia are part of the natural distribution o f Phyllodactylus europaeus, Hemidactylus turcicus, Coluber viridif/avus, Emys orbicularis, Caretta caretta and Dermochelys coriacea, that inhabit other parts of Europe as well. Several species of lizards are in a more or less fierce competition with each other. A. bedriagae for instance is pushed to high altitude, bare rock and granite boulders in little streams, by P. tiliguerta. P. sicula campestris is successful in flat terrain, leaving only walls ofstacked stones toP. tiliguerta. P. s. cettii doesn`t even leave this habitat toP. tiliguerta. As for now P. sicula is restricted mainly to coastal areas, lea- ving the better part of Corsica to P. tiliguerta. D. sardus and D. montalentii are only recently recog- nised as different species. D. montalentii is endemic to Corsica, whereas D. sardus is known too from Sardinia. D. montalentii is living in high altitudes, especially in clear mountain-streams, D. sardus in lower altitudes and has a less specialised preference for its habitat. Corsica is a very interesting island from a herpetolo- gical point ofview.

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The Herpetological Collection of the Trieste Natural History Museum has almost 700 specimens of European Sauria belonging to about 33 taxa, including all the lacertids of northern Adriatic re- gions. The origin of the collection dates back to the foundation of the Museum of Trieste in 1846, but it was increased mainly between 1871 and 1939. The Herpetological Collection of the Trieste Natural History Museum has a great scientific and historical importance; it documents the varia- tion of the composition and distribution of northern Adriatic Sauria fauna during this century, in- cluding endemic varieties typical of little islands.

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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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The chromosome complements of Podarcis filfolensis, P. tiliguerta, P. wagleriana and Archaeolacerta bedriagae were analyzed in bone marrow somatic mitoses as well as in meiotic diakinesis. All four species are characterized by the typical lacertid karyotype consisting of 38 chromosomes (36 acrocentric macrochromosomes plus 2 microchromosomes). Adaptive stability of karyotypes, as a result ofa canalization process of chromosomal evolution, and absence of complex social behaviour promoting population subdivision and inbreeding, are the evolutionary factors presumably correlated with the remarkable conservativeness of karyotype observed within the family Lacertidae.

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We report preliminary data on the natural history and biometry gathered during a short-term study in a Corsian population of the lizard Lacerta bedriagae . Lizards were encountered at heights of 1650-1950 m. Main characteristics of its habitat are the presence of large rocks, boulders and rock pavements. Three size (age) classes were distinguished. Adult males average larger in body size and have larger heads and limbs than females. Females mature at a body size of 66-68 mm. Earth-worms, arthropods and plant leafs were recorded as food items.

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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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Although distribution databases are a dynamic tool, continuously updated, it is important to take “snapshots” of the species distribution over time to promptly identify potential conservation issues. With this work, we provide an update of the distribution of amphibians and reptiles in Sardinia and satellite islands. Data derive from both direct field observations (carried out since 2005 until July 2022) and literature, accounting for over 7000 records: 1416 records of 11 species of amphibians and 5600 records of 18 species of reptiles. Distribution maps (on 10 × 10 km UTM grid) of 29 species are provided in supplementary materials as well as the updated list of the amphibians and reptiles occurring in the circum-Sardinian islands. Most of the meshes were characterized by the presence of 1-3 amphibian species (73%) and 6-8 or 9-11 reptile species (32% with 6-8 species, 30% with 9-11 species). Species abundance was favoured by environmental heterogeneity, and mostly varied in relation to elevation range and edge density.

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The aim of the present study is to synthesise the available data on the occurrence of lacertid lizards on Mediterranean islands better to understand how far human influence is involved in the present distributional patterns of insular lacertid lizard fauna. At present, the Mediterranean islands are inhabited by several lacertid genera, including endemic species of the genera Algyroides (viz. fitzingeri), Lacerta [Archaeolacerta] (viz. bedriagae) and Podarcis (atratus, filfolensis, gaigae, lilfordi, milensis, pityusensis, raffonei, tiliguerta, waglerianus). Recently reported data shed new light on the relationships between these endemics and some continental species that have recently colonised the islands. The arrival of the latter might be directly related to the progressive human colonisation of these islands. The arising conservation problems are also considered.

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Archaeolacerta bedriagae is a Corso-Sardinian endemism, known only from the Corsican Islet La Folaca, but recently discovered on two other islets (Lavezzi satellite islands). All three populations genetically belong to the sub-Corsican clade. The micro-insular distribution of this lizard is limited to the islands and islets of the Strait of Bonifacio. The absence of the Bedriaga`s rock lizard in the Corsican main islands of Lavezzi and Cavallo still remains unexplained; however, for the latter, habitat alterations and the introduction of alien species could be the cause. The absence of the Bedriaga`s rock lizard from the other Lavezzi islets may have been influenced by the morphology and vegetation cover of these islets.

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Climatic conditions changing over time and space shape the evolution of organisms at multiple levels, including temperate lizards in the family Lacertidae. Here we reconstruct a dated phylogenetic tree of 262 lacertid species based on a supermatrix relying on novel phylogenomic datasets and fossil calibrations. Diversification of lacertids was accompanied by an increasing disparity among occupied bioclimatic niches, especially in the last 10 Ma, during a period of progressive global cooling. Temperate species also underwent a genome- wide slowdown in molecular substitution rates compared to tropical and desert-adapted lacertids. Evaporative water loss and preferred temperature are correlated with bioclimatic parameters, indicating physiological adaptations to climate. Tropical, but also some popu- lations of cool-adapted species experience maximum temperatures close to their preferred temperatures. We hypothesize these species-specific physiological preferences may con- stitute a handicap to prevail under rapid global warming, and contribute to explaining local lizard extinctions in cool and humid climates.

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An electrophoretic investigation of 17 gene loci in 11 populations of Meditteraneans lacertids (Podarcis muralis, P. tiliguerta, P. hispanica, P. sicula, `Archaeolacerta` bedriagae) completed with a dendrogram after unweighted pair groups` arithmetic average cluster analysis of NEI genetic identity values, show: - important differences between Podarcis muralis and Podarcis tiliguerta, apparently sufficient to justify the maintenance of this taxon at the specific level; - important differences between animals of Archaeolacerta, Podarcis and Lacerta s. str. (MAYER et TIEDEMANN, 1982) which would allow to raise Archaeolacerta at a generic statute. This study allows equally to establish the diminution of percentage of polymorphic loci for micro-insular P. tiliguerta populations according to the removal from Sardinia and the estimate separation`s time. A tentative phylogenetic explanation is done by the authors.

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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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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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Es wird über den Fund von Archaeolacerta bedriagae am Monte Pino in Nordost-Sardinien berichtet. Die Eidechsen wurden an einer kleinen Felsgruppe in der Gipfelregion (742 m ü. NN) beobachtet. Die Verfasser vermuten, dass die Art reliktartig verbreitet ist.

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The gaps as yet existing in our knowledge on the palaeogeography of the Mediteranean area, one of the most geologically «restless» on the globe, the scarcity of palaeontological data on amphibians and reptiles (often identified or identifiable only as far as the genus or family) as well as the uncertainties on the systematic position and true relationships of several of the taxa involved make many of the following conclusions on the origins of the herpetological population of Sardinia opinable. This population seems to have occurred i n at least five periods: 1) premiocenic age (taxa deriving from ancestors already present on the Sardinian Corsican microplate prior to its detachment from the main European plate): Euproctus platycephalus, Hydromantes genei, Discoglossus sardus?, Phyllodactylus europaeus??, Algyroides fitzingeri?, Archaeolacerta bedriagae?, Podarcis tiliguerta?; 2) messinian age (salinity crisis of the Upper Miocene), from European or African areas: Hydromantes flavus, Hydromantes imperialis, Hydromantes n.sp., Discoglossus sardus? Hemìdactylus turcicus??, Tarentola mauritanica??, Phyllodactylus europaeus?, Algyroides fitzingeri?, Archaeolacerta bedriagae?, Podarcis tiliguerta?, Chalcides chalcides?, Chalcides ocellatus?, Coluber hippocrepis?, Natrix natrix?, Natrix maura? 3) pliocenic age: Bufo viridis?, Hyla sarda, Hemìdactylus turcicus??, Tarentola mauritanica??, Natrix natrix?; 4 ) pleistocenic age (Cassian regression), from Tuscany across the so-called Elba-Brücke: Bufo viridis? Emys orbicularis, Testudo hermanni?, Hemìdactylus turcicus?, Tarentola maurìtanica?, Podarcis sicula?? Coluber viridiflavus, Elaphe longissima?, Natrix natrix?; 5) protohistoric and/or historic period (transport by man followed by acclimatization): Rana sp. plurimae of the «Rana escidenta-complex», Testudo graeca, Testudo marginata, Hemìdactylus turcicus?, Tarentola mauritanica?, Podarcis sicula?, Chalcides chalcides??, Chalcides ocellatus??, Coluber hippocrepis??, Elaphe longissima?, Natrix maura??, Testudo hermanni?.

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Immunological reactions tested according to Libby`s photronreflectometric technique show that: (i) Archaeolacerta Mertens, 1921, and Podarcis Wagler, 1830, are independent genera and not subgenera of Lacerta Linnaeus, 1758; (ii) Podarcis muralis (Laurenti, 1768), Podarcis sicula (Rafinesque, 1810), Archaeolacerta bedriagae (Camerano, 1885), Archaeolacerta monticola (Boulenger, 1905), Lacerta lepida Daudin, 1802, Lacerta schreiberi Bedriaga, 1878 and Lacerta viridis (Laurenti, 1768) are full species; (iii) Podarcis tiliguerta is a subspecies of P. muralis: P. muralis tiliguerta (Gmelin, 1789).

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Chemosystematic investigations on the position of Lacerta jayakari and the genera Gallotia and Psammodromus (Sauria; Lacertidae) 13 species of the genera Lacerta, Psammodromus and Gallotia (L. erhardii, L. filfolensis, L. bedriagae, L. cappadocica, L. jayakari, L. vivipara, L. trilineata, L. agilis, P. hispanicus, P. algirus, G. atlantica, G. galloti, G. stehlin:) have been examined by means of micro complement fixation tests (albumin) as well as by proteinelectrophoresis concerning 14 genetic loci. The results and their con-sequences are the follows: 1. L. cappadocica, L. bedriagae, and L. erhardii/L. filfolensis are representatives of phylogeneticly equivalent groups (subgenera). Their isolation in the Middle Miocene corresponds with the first contacts of the landmasses of Eurasia and Africa. 2. Lacerta jayakari may be considered as a representative of a further group equivalent in this aspect; though the immunological results would not exclude a position near the green lizards (subgenus Lacerta s. str.). 3. Because of this isolated position of L. jayakari for this species (and Lacerta cyanura) the subgenus Omanosaura subgen. nov. has been established. 4. Psammodromus hispanicus and P. algirus have probably been isolated of each other since the Middle Miocene, too. 5. The radiation of the genus Gallotia corresponds closely with genesis of the Canary Isles.

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Albumins from several species assigned to Lacerta s. 1. and Gallotia were investigated by means of the Micro-Complement fixation technique. The phylogenetic trees evaluated according to Fitch & Margoliash (1967) and Beverley & Wilson (1982) led us to infer a division, which is in accordance with protein electrophoretic results (Mayer & Tiedemann, 1982) as well as with the subgeneric division used before the studies of Böhme (1971) and Arnold (1973).

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Parts of the mitochondrial genes coding for 12SrRNA and 16SrRNA (together about 960 bp) were sequenced for all Mediterranean species of `Mountain lizards` of the genera Archaeolacerta (sensu lato) and Iberolacerta. All subspecies of the Iberian species Iberolacerta cyreni and I. monticola were included in this study. In addition, samples of Apathya cappadocica and Darevskia rudis were analysed to elucidate the relationships of the European `Mountain lizards` to their possible relatives in the Near East. Maximum parsimony and neighbour joining analyses lead to the following major conclusions: (i) the monophyly of the genus Iberolacerta is very well supported; (ii) Archaeolacerta bedriagae (the type species of the genus) is most basal with respect to the ingroup taxa. If we accept Iberolacerta as a genus, Archaeolacerta becames paraphyletic. Therefore, we propose to restrict Archaeolacerta to the type species and to treat A. mosorensis and A. oxycephala provisionally as members of the collective genus Lacerta; (iii) within the genus Iberolacerta three groups were found: a Pyrenean group, an Iberian group and I. horvathi. The relationships among these groups remain unresolved; and (iv) the Peña de Francia lizards, described originally as a subspecies of I. cyreni, are in fact more closely related to I. monticola.

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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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Investigated the albumins from 31 species and subspecies of the genus Lacerta s.1. by means of the immunoloical techniue Micro-Complement-fixation. Dendrograms were computed by means of the ktch-MargJiash algorithm. Moreover the taxa of the Lacerta saxicola and the Lacerta danfordi comlexes were analyzed by electrophoresis concerning 14 genetic loci. The results were discussel together with karyological and genitalmorphological data so far known yielding the following relationships: Lacerta graeca shows a closer relationshi to the subgenus Podarcis as does the quite closely related species air L. dugesii and L. perspicikata. Lacerta Iaevis probabl is connected closely to Podarcis, too. Lacerta parva shows a closer relationship to the `small izards` than to the sub-genus Lacerta s. str. A clear decision concerning the position of the Lacerta danfordi complex according to chemosystematical data was not possible. It is isolated from the other species probably about as long as L. puma. Biochemical differences between its `species` are too small to confirm their taxonomical revalorisation by Eiselt and Schmidtler Within the Lacerta saxicola complex the investigated taxa show a close relationship. Lacerta praticola and L. derjugini were definitly assigned to this group.

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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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10 species (peloponnesiaca, muralis, melisellensis, graeca, oxycephala, horvathi, bedriagae, vivipara, viridis, agilis) of the genus Lacerta were examined by employing protein electrophoretic data for 16 genloci. Gene frequencies are given and genetic distances calculated according to NEI (1971, 1972). These and former attempts to subdivide the genus Lacerta are discussed. The electrophoretic results provide the possibility of a classification of the examined species into groups at the subgenus level corresponding to those valid before BÖHME (1971) and ARNOLD (1973): genus Lacerta subgenus Lacerta s. str. subgenus Podarcis subgenus Archaeolacerta subgenus Zootoca

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The collection of Amphibians and Reptiles of the Museum of Natural History of Ferrara has characteristics of historical representation, taxonomic and zoogeography that may be considered as examples of medium-sized types of collections more preva- lent in Italian museums. It consists of a historic part of the study and a donation from Guido Campadelli. The collection consists of 1739 specimens of amphibians (1734 of which held in 437 containers with ethanol and 5 taxidermized specimens) for a total of 78 amphibian species. There are 811 specimens of Reptiles (769 of which are stored in 526 containers with ethanol and 42 taxidermized specimens) representing a total of 108 species. The findings that form the collection of Amphibians come from 153 loca- lities of 15 states and 12 regions and 29 provinces of Italy. In the batrachological col- lection 62.1% of the total European species, and 94.3% of the total species in Italy, are represented. Zoogeographic regions most represented are the Palaearctic with 67% of the species of Amphibians in the collection and the Neotropical with 29%, fol- lowed by the Ethiopian (6%) and Nearctic (5%). Reptiles specimens come from 247 lo- calities of 15 states and 15 regions and 36 provinces of Italy. In the collection 46,2% of European species and 91,5% of the Italian ones are represented. The most represen- ted zoogeographic region are the Palaearctic with 89% of species in the collection, followed by the Ethiopian (14%), the Eastern (13%), Neotropical (11%) and the Nearctic (7%); australian and malagasy species do not exceed 3%. The herpetology collection was the subject of taxonomic and biogeographic analysis.

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A description of the beautiful island of Corsica and of its richness of reptiles and amphibians. The lizard which is most frequently found in the island, Lacerta muralis tiliguerta, is a splendid animal he met with everywhere. In the mountains, above 1000 meters, he found the likewise very fine lizard Lacerta bedriagae bedriagae wtth the cobalt blue lateral shields. This species is very alert and hard to get. Especially in moist regions the most individuals are to be found. Amphibians were plentiful in the neighbourhood of Calvi (N. Corsica). Tadpoles were found of Hyla arborea sarda (de B e t t a), and of Discoglossus pictus sardus T s c h u d i, together with young Buto viridis viridis Laurenti. Also near Calvi Emys orbicularis L i n n e and a lot of grass snakes were found. If anyone might go to Corsica on herpetological purposes he should visit the reservoir near Argentella, for there is a real meeting place of reptiles and amphibians.

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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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The authors report about their observations on coastal populations of Archaeolacerta bedriagae on Corsica, where these lizards live on coastal rocks. Furthermore, a blue-tailed colour morph is described.

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ventaire exhaustif des espèces indigènes et naturalisées, présentes e n France et au Benelux : 85 taxons, relevant de 72 espèces, sont cités, mais deux autre s taxons, dont le statut reste à définir, sont mentionnés au n os 31 (Rana esculenta) et a u n° 53 (Podarcis muralis) et huit autres au n` 56 (Podarcis muralis tiliguerta) de l`inven- taire. On signale les zones à prospecter par priorité et les problèmes taxonomiques à résoudre d`urgence . Les aires sont définies par rapport aux provinces ou aux départements : des cartes d`aire provisoires, en France, sont données pour 33 taxons. En ce qui concerne la liste des taxons relatifs à la France, les modifications suivante s sont à noter : 1°) taxons admis : Triturus alpestris apuanus, Acanthodactylus erythrurus cf. erythru- rus, Lacerta agilis garzoni, Podarcis hispanica hispanica, Podarcis muralis merremia , Vipera latastei latastei, Vipera seoanei ; 2.) deux intergrades de Salamandra salamandra sont retenus : 30) taxons refusés : Rana iberica, Coronella austriaca fitzingeri, Natrix tessellata tessellata ; 4.) tombent en synonymie les deux taxons suivants : Podarcis muralis occidentalis (= P. m. muralis) et P. m. calbia (= P. m. oyensis). En outre, liste des espèces introduites, liste des espèces citées par erreur et list e des taxons à rechercher . Quelques données inédites concernent le nord de l`Espagne .

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Lacertinae is one of the three lacertid lizard subfamilies with a geographical distribution confined to the Palaearctic. Several past attempts to reconstruct its phylogeny resulted in unresolved bush-like topologies. We address the question of whether the lack of resolution is due to insufficient data or whether this lack reflects a rapid succession of speciation events. We analyzed four partial and one complete gene sequences from mitochondrial and nuclear genomes, totalling roughly 3600 bp. We included 29 species representing all 19 genera suggested in recent revision of Lacertinae [Arnold, E.N., Arribas, O., Carranza, S., 2007. Systematics of the palaearctic and oriental lizard tribe Lacertini (Squamata: Lacertidae: Lacertinae), with descriptions of eight new genera. Zootaxa 1430, 1–86]. The resulting phylogeny, first, corroborates monophyly at the genus level for the suggested genera, as well as the finding that Atlantolacerta andreanskyi, until recently part of Lacertinae, belongs to the subfamily Eremiadinae. Second, we find that increasing the sequence length and combining multiple nuclear and mitochondrial sequences did not resolve the polytomy, suggesting that the inferred topology indicates a multiple cladogenesis within a short geological period, rather than a methodical artefact. Divergence time estimates, based on previous estimates of several node ages, range from 13.9 to 14.9 million years for the radiation event, however with very broad confidence interval. To associate the radiation with a narrower geological time we consider palaeogeographic and palaeoclimatic data, assuming that the Lacertinae probably evolved in Central Europe andWAsia after the collision of Africa and Eurasia. We suggest that this radiation may date to the late Langhian (ca. 14–13.5 million years) when geological events caused abrupt changes in regional water–land distribution and climate, offering a window of distinct conditions.

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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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Here we report on the combined observations of 10 years of opportunistic field work conducted during short visits to Sardinia, from 1999 to 2012. A total amount of 433 distribution records of 27 species were collected from 187 different localities covering 52 unique UTM squares. We report species presence in 157 new UTM squares and additionally reconfirm previous reported presence in 150 UTM squares. Overall, we produce a remarkable increase in the knowledge of the Sardinian herpetofauna. Notes and observations on ecology, taxonomy and conservation are provided.

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Common Italian names of the amphibians and reptiles present in the geographic Italy are proposed. We analysed a large set of bibliography in order to assess a list of Italian common names used and we proposed the utilization of a single name, also in view of the forthcoming publication of the distribution atlas of the Italian herpetofauna. The criteria used to assign such names follow in general the current use, the possibility to clearly distinguish similar species, geographic and linguistic parameters.

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The link between ecology and economies is manifest over the umrld as a result of long-term processes. But because these processes are long term, it is bard to prove the link. On Sardinia serious economic development was late to arrive, having occurred only over the last few decades. As a case study, research was carried out for 10 years on the state of nature as well as the economic growth in one of the least developed areas abutting the Gulf of Orosei on the east coast Based on research and lasting attention to political affairs concerning the projecg we formulate general recommendations for the area In 1995, the Italian Government will he asked by the European Government to undertake serious steps to save endemics (especially herpetofauna) of Europe`s last pristine areas.

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Sardinia shows a clear lack of herpetological data due to an evident paucity of herpetological surveys. This gap of knowledge is worthy of attention, since Sardinia hosts a rich herpetofauna with a large proportion of endemic species, and distribution data are crucial for targeting conservation efforts. In this paper we provide new distribution data for Sardinian reptiles, with the aim of updating our knowledge on their specific distribution. Data were opportunistically recorded during ten years of field research in Sardinia, carried out in more than twenty campaigns from April 1999 to June 2009. All the eighteen reptile species belonging to the Sardinian fauna were recorded. A total amount of 293 faunistic data were collected from 178 different localities covering the entire study area. Within this dataset, 137 faunistic data fall outside known species’ ranges as reported in the Atlas of Italian amphibians and reptiles. In conclusion, data presented here produced a remarkable increase of knowledge on Sardinian reptiles distribution compare to that reported in the last available syntheses. Nevertheless, it should be evidenced that, notwithstanding the present updating, the knowledge of Sardinian reptiles’ distribution is probably still far from being exhaustive. Thus, further investigations are strongly required for obtaining a complete picture and identifying conservation priorities in terms of isolated species/populations and areas of high diversity and endemicity.

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Archaeolacerta bedriagae (Camerano, 1885) is a rock lizard endemic to Corsica and Sardinia. Based on weak morphological traits four subspecies have been described to date. The nominal subspecies (A. b. bedriagae) occurs on Corsica. The three following subspecies inhabit different geographic areas of Sardinia: A. b. sardoa (Gennargentu Massif), A. b. paessleri (Limbara Mountains), A. b. ferrerae (coastal Gallura). Allozyme variation in A. bedriagae was previously investigated by Guillame and Lanza (1982). These authors compared three populations only (one from Corsica and two from Sardinia) and obtained very high values of Nei’s genetic distance, ranging from 0.172 to 0.309. However, the values of genetic distance indicated by those authors were completely wrong because of miscalculation. On a subsequent paper Guillame (1987) proposed a different genetic scenario, indicating corrected values of Nei’s genetic distance among the three A. bedriagae populations, ranging from 0.133 to 0.186. These values, although being much lower than those estimated by Guillame and Lanza, are in fact very high, falling into the range obtained from comparisons between well recognized biological species of the genera Lacerta and Podarcis. In spite of this, Guillaume (1987) proposed to synonymised two subspecies (A. b. paessleri and A. b. ferrerae), and Lanza (1983) questioned the systematic validity of the Sardinian subspecies. On the other hand, based on the genetic data reported by Guillame and Lanza, Arribas (1999) hypothesized the occurrence of unrecognized species of the genus Archaeolacerta within the Corso-Sardinian area. In addition, in a paper devoted to the systematics of the tribe Lacertini, Arnold et al. (2007) found considerable mitochondrial DNA variation among three Corsican individuals of A. bedriagae, and hypothesized the occurrence of more than one species. In this paper allozyme variation of A. bedriagae was studied, and the results were compared with those obtained in previous studies. A total of 55 individuals from 5 Corsican (Roccapina) and Sardinian (Punta Falcone, Limbara Mountains, Gennargentu Massif, Mount Settefratelli) localities were used. All recognized subspecies were included in the analysis, plus one sample from southern Sardinia (Mount Settefratelli) for which the recognition of the subspecific status was suggested. For interspecific comparison, 11 individuals of Iberolacerta cyreni (Müller & Hellmich 1937) from Central Spain (Sierra de Guadarrama) were also analyzed. Approximately 2 cm of the tail tip of each lizard was taken off, in order to avoid killing animals, and stored below -70°C until electrophoretic analysis. Standard horizontal starch gel electrophoresis was performed on muscle tissue homogenates using buffer systems and procedures described by Capula. Gene products for the following 20 presumptive gene loci were analaysed,: αGpd, Ldh-1, Ldh-2, Mdh-1, Mdh-2, Me-1, Me-2, Idh-1, Idh-2, 6Pgd, Sod-1, Ak, Pgm-1, Pgm-2, Ck, Mpi, Gpi, Est-1, Gp-1, Gp-2. Genotype and allele frequencies were determined by direct count from allozyme phenotypes. The genetic relationships among the populations studied were evaluated using Nei’s standard genetic distance (D). The phenetic relationships among populations were estimated by means of the UPGMA method. Eleven out of 20 loci were found to be monomorphic, i.e. fixed for the same allele, in all populations (αGpd, Ldh-2, Mdh-1, Mdh-2, Idh-2, Sod-1, Ak, Pgm-1, Pgm-2, Gp-1, Gp-2). Three out of nine polymorphic loci were weakly polymorphic (Ldh-1, Me-2, Mpi). Lizards from Corsica were characterized by two unique alleles, i.e. Mpi102 and 6Pgd95. Four unique alleles were found in the Sardinian populations: Est-1102 in all populations, Me-295 in the population from the Limbara Mountains, 6Pgd105 and Ldh-195 in the populations from the Mount Settefratelli. Low levels of genetic differentiation were found in A. bedriagae, Nei’s D ranging from 0.013 to 0.042, with an average genetic distance of 0.026 (SD = 0.010). A similar value of Nei’s D was found between Corsican and Sardinian populations (D = 0.025; SD = 0.008). The sample from the Mount Settefratelli (southern Sardinia) was considerably differentiated from the other ones (average D = 0.032; SD = 0.011). Low Nei’s genetic distance values were found comparing the four recognized subspecies (average D = 0.023; SD = 0.007). Our results are not in accordance neither with those reported by Guillame and Lanza, nor with those by Guillame (1987), clearly indicating low levels of genetic differentiation among populations. Genetic differentiation among the recognized subspecies resulted to be much lower than the one estimated by Guillame and Lanza (1982). Our results are in agreement with the mitochondrial DNA analyses, the nuclear markers analyses and the morphometric analyses. This would indicate that the supposed occurrence of a unrecognized Archaeolacerta species within the Corso-Sardinian Plate is not supported by genetic data.

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Archaeolacerta bedriagae is a rock lizard endemic to Corsica and Sardinia. Four subspecies have been recozied to date on the basis of morphological traits. Previous allozyme investigations revealed high genetic differentiation among populations of the species. Based on these results some authors hypothesized that more than one species of Archaeolacerta may occur on Corsica and Sardinia. In this paper we investigated allozyme variation at 19 gene loci in 5 populations belonging to all subspecies of A. bedriagae in order to study genetic differentiation among populations from Corsica and Sardinia, and to compare our results with those obtained in previous studies carried out on allozyme variation and taxonomy of the species. Low levels of genetic differentiation (average Nei`s D = 0.026) and heterogeneity (mean FST = 0.147) were found comparing the A. bedriagae populations, and there was no evidence of interruption or restriction of gene flow. This is in agreement with the available molecular and morphometric data, while it is not in accordance with allozyme data reported in the previous studies. Our data do not support the hypothesis of an unrecognized criptic species of Archaeolacerta in Corsica and Sardinia, and indicate that the definitive assessment of the taxonomic status of the A. bedriagae populations requires further investigation.

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The peculiar bioclimatic and geographic features of Corso–Sardinian islands may provide an ideal scenario for investigating microevolutionary processes, given their large heterogeneity of environments, which could affect dispersal and gene flow among populations, as well as processes of local adaptation. The genetic variation and differentiation among populations of the endemic lizard Archaeolacerta bedriagae were studied by allozyme electrophoresis at 20 presumptive loci. The genetic structure of this species is characterized by relatively high levels of polymorphism and low differentiation among populations. The pattern of genetic differentiation cannot be explained by genetic drift as a function of geographic distance. Genetic distance data show that genetic variation is distributed into three geographically coherent population groups and suggest a recent (Late Pleistocene) origin for the observed geographic fragmentation. The analysis of environmental correlates of allozymic variation indicates a strong correlation of the Idh-1 locus with climatic variables. The frequency of the Idh-1106 allele is negatively correlated with annual temperature, and positively correlated with annual precipitation. In addition, the observed heterozygosity at this locus decreases towards more arid climatic regimes. The results obtained support the assumption of differential selection acting on Idh-1 allozymes under diverse climates. An association between Idh-1 allozymes and local bioclimatic regimes was also observed for the sympatric lizard Podarcis tiliguerta, suggesting a key role for such selective agents on Idh-1 polymorphism in these two Corso–Sardinian lacertids.

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Corsica and Sardinia are important hotspots of diversity and endemism. Surprisingly, only a few studies are available on geographic variation and evolutionary history of Corsican-Sardinian species. In this study we investigate biogeographic and evolutionary patterns of three lacertid lizards endemic to Corsica and Sardinia under a comparative phylogeographic framework. We analysed mitochondrial gene genealogies in Archaeolacerta bedriagae, Podarcis tiliguerta, and Algyroides fitzingeri including populations from the entire species’ distribution range. Preliminary results show a complete lack of phylogeographical concordance among significant genealogical partitions across the studied species. Each species shows an idiosyncratic pattern of geographical distribution of genetic diversity and a different degree of differentiation among the main lineages with P. tiliguerta likely representing a species-complex, A. bedriagae showing two main (well differentiated) lineages and A. fitzingeri showing a very low differentiation among populations. Based on these preliminary results, the absence of common phylogeographic patterns in these three co-distributed species would reflect a complex of historical, evolutionary and biogeographical processes within the Corso-Sardinian biota. Further investigations with the inclusion of nuclear markers are needed for a better understanding of the complexity of the processes underlying the origin and the patterns of diversity in endemic reptiles from Corsica and Sardinia.

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Archaeolacerta bedriagae is a rock-dwelling lizard endemic to the Corso-Sardinian insular system. We investigated the phylogeography of the species by using the mitochondrial ND4 and flanking tRNAs genes from 94 specimens belonging to 19 populations. Phylogenetic, Barrier, and SAMOVA analyses revealed a highly structured pattern characterized by two levels of discontinuities in the geographical distribution of mtDNA diversity: (i) a deep phylogeographic break in Northern Corsica between Lineage A, restricted to northernmost Corsica, and Lineage B widespread all over the remaining range of the species, and (ii) some minor phylogeographic discontinuities within lineage B, which is sub-structured into six closely related haplotype clades with remarkable concordance with geography. The first evolutionary event concerning the split between the two main lineages from an ancestral population occurred in the Upper Pliocene (5.87–3.68 mya), while the divergence within lineage B would have started from the Upper Pleistocene (2.5–1.6 mya), between Corsican and Sardinian populations. Somewhat later (1.7–1.1 mya), the Sardinian ancestral population underwent fragmentation into population groups inhabiting North, Central, and South Sardinia. As inferred from previous allozyme surveys, the divergence among population groups would be driven by allopatric fragmentation, while the discrepancy concerning the major partition into two lineages inferred from mtDNA but not apparent in analysis of allozymes needs further investigation.

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Archaeolacerta bedriagae is a rock lizard endemic to Corsica and Sardinia. Four subspecies have been described based on weak morphological traits: the nominal one spread in Corsica and the remaining three in Sardinia (sardoa, paessleri and ferrerae, respectively in the Gennargentu Massif, Limbara mountains and coastal Gallura). Recent analyses of both allozyme and morphological variability did not support this subspecific arrangement (Salvi et al., unpubl.). Phylogeographic structure and relationships of 13 populations, representing the whole range of A. bedriagae, were analysed using mitochondrial sequences of nad4 and tRNA His genes. Genomic DANN was extracted from tail tips of 64 specimens and a fragment of 850 bp was amplified by PCR using ND4 and Leu primers. Sequences (from GenBank) of four species belonging to the genera Podarcis and Lacerta were employed as outgroups. Phylogenetic analyses were performed under the assumptions of both maximum parsimony (MP) and distance (NJ). We also analysed the genealogical relationships among the 19 haplotypes found by a statistical parsimony network. Both phylogenetic and haplotype network analyses showed the same geographical structure of genetic variability. The northern Corsica population appeared deeply differentiated from the remaining ones, whereas the southern Corsica population represented the sister group of the Sardinian populations. In Sardinia we identified three major groups distributed from North to South, being the Southernmost fairly differentiated from the others. The most parsimonious biogeographical hypothesis indicates an ancient colonization from southern Corsica to Sardinia, where considerable fragmentation into population groups subsequently occurred.

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We analysed the species–area relationship and structural connectivity among islands of La Maddalena Archipelago (Italy), a numerous group of small islands very close to Sardinia. We related species richness (amphibians and reptiles) to several environmental factors (area; number of unique habitats; topographical variables; and distances of each island to Sardinia, to the nearest island and to the nearest large island) using generalized additive models and connectivity analysis by graph theory and the software Conefor 2.6. Using each method, we performed several comparisons: considering all species; excluding species with a high exchange rate (‘in transit’); including only autochthonous species; and including species present on large islands. We also excluded, in turn, all amphibians; all Scincidae; all Gekkonidae; all Lacertidae; all Colubridae; and one species in turn. Except in the case of species present on large islands, all models selected the same variables: ruggedness standard deviation, area, number of unique habitats, and mean and maximal elevation. When excluding Sardinia, the highest connectivity value corresponded to the largest islands. Species richness is related to island complexity (habitat diversity and topographical complexity) and not simply to area. Network connectivity is dominated by the internal connectivity of the largest islands, but small islands are essential to maintain the network connectivity and endemicity.

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This paper represents an update of the list of Italian amphibians and reptiles published 15 years ago by Razzetti et al. (2006) and of the checklist published in 1993 by the late Benedetto Lanza. At present, the Italian herpetofauna includes 100 species (41 amphibians and 59 reptiles) and an amphibian taxon of hybrid origin. Seven species and one subspecies are allochthonous and became naturalized within the last century. Since the last published list, a new species has been described (Vipera walser), five taxa have been raised to species rank (Salamandrina perspicillata, Speleomantes sarrabusensis, Zootoca carniolica, Malpolon insignitus and Natrix helvetica) while three taxa have been downgraded to subspecies. All the relevant taxonomic changes based upon new research have been discussed, including tentative revisions and controversial taxa. Nine species reported or listed dubitatively in Lanza’s 1993 list are excluded here.

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Research on the taxonomy of European amphibians and reptiles has increased noticeably over the last few decades, indicating the need for recognition of new species and the cancellation of others. This paper provides a critical review of recent changes and draws up a tentative species list.

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The last species list of the European herpetofauna was published by Speybroeck, Beukema and Crochet (2010). In the meantime, ongoing research led to numerous taxonomic changes, including the discovery of new species-level lineages as well as reclassifications at genus level, requiring significant changes to this list. As of 2019, a new Taxonomic Committee was established as an official entity within the European Herpetological Society, Societas Europaea Herpetologica (SEH). Twelve members from nine European countries reviewed, discussed and voted on recent taxonomic research on a case-by-case basis. Accepted changes led to critical compilation of a new species list, which is hereby presented and discussed. According to our list, 301 species (95 amphibians, 15 chelonians, including six species of sea turtles, and 191 squamates) occur within our expanded geographical definition of Europe. The list includes 14 non-native species (three amphibians, one chelonian, and ten squamates).

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Three species of lacertid lizards (Lacerta bedriagae, Podarcis tiliguerta, and Podarcis sicula) are able to detect the former presence of the saurophagous snake Coluber viridiflavus by tongue flicking. Lizards tongue flicked more in cages previously inhabited by the predatory snake than in clean cages or in cages treated with eau-de-cologne. They also exhibited behavioral acts typically associated with stressful situations (foot shakes, tail vibrations, starts) more frequently when predator chemicals are present. Individuals from the two Podarcis species that came from populations syntopic with C. viridifiavus were also able to distinguish between chemical cues from this saurophagous predator and a nonsaurophagous snake (Natrix maura). In these lizards, the former presence of N. maura did not elicit higher tongue-flick rates or stress-indicating behaviors. In contrast, individuals of Lacerta bedriagae collected from a snake-free area increased tongue-flick rate and frequency of stress-related behavior in response to chemicals of both snakes, suggesting that prior contact is not required for chemosensory recognition of snakes in this species but may facilitate the distinction between different species of snakes. The presence of predator (C. viridiflavus) chemical cues induces a shift in the microhabitat use of the lizard species studied. In a large terrarium containing various substrates, lizards chose different types of microhabitats when chemical cues of C. viridiflavus were present than when absent and avoided the side of the terrarium labeled with the chemicals.

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We tested the hypothesis that an evolutionary trade-off exists between the capacity to run on level terrain and the ability to climb inclined structures in lacertid lizards. Biomechanical and physiological models of lizard locomotor performance suggest that the morphological design requirements of a ground-dwelling vs. scansorial life style are difficult to reconcile. This conflict is thought to preclude simultaneous evolution of maximal locomotor performance on level and inclined terrain. This notion has been corroborated by comparative studies on lizard species from other groups (Anolis, Chamaeleo, Sceloporus), but is not supported by our data on 13 species from the family Lacertidae. We found no indication of a negative association between maximal sprint speed of lizards over a level racetrack (indicative of ground-dwelling locomotor performance), on an inclined stony surface (indicative of climbing performance over rock faces) and inclined mesh surface (indicative of clambering performance among vegetation). Moreover, morphological characteristics associated with fast sprinting capacities (e.g. long hind limbs) apparently enhance, rather than hinder climbing and clambering performance. We conclude that in our sample of lacertid lizards, the evolution of fast sprinting capacity on level terrain has not inflicted major restrictions on climbing and clambering performance.

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The aim of this study was to determine if divergence in habitat use among lacertid lizards is paralleled by morphological differentiation. For 35 lacertid species, we measured body, head and limb dimensions. Habitat use was inferred from the literature: ground-dwelling on open terrain, ground-dwelling in vegetated areas, shrub-climbing, tree-climbing, saxicolous (i.e. rock-climbing). Traditional (i.e. non-phylogenetic) statistical analyses suggest morphological differences among species groups with different habitat use. Ground-dwelling species from open habitats tend to have longer femurs, tibiae and humeri (relative to body length) than other groups. Cursorial (i.e. level-running) species have relatively high heads and trunks compared to climbing species. These differences follow biomechanical predictions and it is tempting to consider tham as adaptations to habitat use. However, phylogenetic analyses of the data fail to establish a clear relationship between habitat use and morphology in the data set considered. There is a weak indication that the differences in head and trunk height have evolved as an adaptation to different habitat use, but the differences in relative limb dimensions among species groups with different habitat use vanish. Either adaptation of limb dimensions to habitat use has not occurred in lacertid lizards, or our methods are unable to demonstrate such an adaptation. We show that uncertainties in the topology of the phylogenetic tree used are unlikely to influence the outcome of our study. We also address the fact that habitat use is often similar in different branches of the phylogenetic tree, and the consequences this may have for the power of our statistical analyses.

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Microhabitat use and antipredator behaviour (i.e. behavioural response to a bird model and refuge microhabitat) was measured in an experimental set-up for 11 lacertid lizard species. Additionally, locomotor performance (sprint speed, climbing and clambering speed, manoeuvrability and endurance) of the same species was quantified. The results showed considerable interspecific variation in microhabitat use, behavioural response and choice of refuge microhabitat. Part of that variation could be linked to differences in locomotor capacity. Species that frequently made use of open microhabitats tended to be fast sprinters, but had limited endurance. The behavioural data suggest these species will not start running before the predator is close at hand, and thus having high sprint capacities might be more beneficial than great endurance. Species that spent most of their time on vertical elements appeared to be fast climbers. As such microhabitats tend to be quite exposed, lizards living there are conspicuous to predators and being able to escape fast seems relevant. Contrary to our expectations, species mostly observed in the vegetated microhabitats did not excel in clambering capacity or manoeuvrability. Possibly, dense vegetation constitutes a safe harbour and species may no longer be under selection for locomotor speed. Behavioural response when confronted with an aerial predator was context-dependent in most species: most lizards fled more when in open or vertical microhabitats than when in densely vegetated ones. Moreover, when fleeing most species sought refuge in the vegetation. These findings support our idea that vegetated patches may constitute a safe harbour for lacertids.

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Morphological and physiological considerations suggest that sprinting ability and endurance capacity put conflicting demands on the design of an animal`s locomotor apparatus and therefore cannot be maximized simultaneously. To test this hypothesis, we correlated size-corrected maximal sprint speed and stamina of 12 species of lacertid lizards. Phylogenetically independent contrasts of sprint speed and stamina showed a significant negative relationship, giving support to the idea of an evolutionary trade-off between the two performance measures. To test the hypothesis that the trade-off is mediated by a conflict in morphological requirements, we correlated both performance traits with snout-vent length, size-corrected estimates of body mass and limb length, and relative hindlimb length (the residuals of the relationship between hind- and forelimb length). Fast-running species had hindlimbs that were long compared to their forelimbs. None of the other size or shape variables showed a significant relationship with speed or endurance. We conclude that the evolution of sprint capacity may be constrained by the need for endurance capacity and vice versa, but the design conflict underlying this trade-off has yet to be identified.