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In the herpetological collection of ZFMK 528 scientific species group names are represented by type materi- al. Of these, 304 names are documented by primary type specimens (onomatophores) while for 224 further names sec- ondary type specimens (typoids) are available, ranging chronologically from 1801 to 2010. The list is a shortened pred- ecessor of a comprehensive type catalogue in progress. It lists name bearing types with their catalogue numbers includ- ing information on further type series members also in other institutions, while secondary types are listed only by pres- ence, both in ZFMK and other collections including holotype repositories. Geographic origin and currently valid names are also provided.

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Presently, the lacertid fauna of Turkey consists of 67 species and subspecies. Since 1990 one species has been recorded as new for Turkey (Acanthodactylus schreiberi), and four species (Darevskia dryada, D. `bendimahiensis`, D. `sapphirina`, Lacerta cyanisparsa) and two subspecies (D. valentini spitzenbergerae, D. raddei vanensis) were newly described. Contrastingly, the formerly listed D. r. raddei does not occur in Turkey. Furthermore it is proposed to reject Parvilacerta parva from the fauna of the European part of Turkey until its presence there has been confirmed, and to reject Darevskia mixta from the Turkish herpetofauna until the record has been confirmed or the material has been re-examined. In addition, an overview on taxonomical changes and new distributional data regarding Turkish lacertids since 1990 is given. Finally, a checklist of all taxa currently known from Turkey is presented.

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Turkey is biogeographically diverse and consequently has a rich herpetofauna. As a result of active herpetological research, the number of species has steadily increased in recent years. I present here a new checklist of amphibian and reptile species distributed in Turkey, revising the nomenclature to reflect the latest taxonomic knowledge. In addition, information about the systematics of many species is also given. In total 35 (19.4%) amphibian and 145 (80.6%) reptile species comprise the Turkish herpetofauna. Among amphibians, 16 (45.7%) anurans and 19 urodelans (54.3%) are present. Among reptiles, 11 (7.6%) testudines, 71 (49%) saurians, 3 (2.1%) amphisbaenians and 60 (41.3%) ophidians are considered part of the herpetofauna. The endemism rate in Turkey is considered relatively high with a total of 34 species (12 amphibian species – 34.3% and 22 reptile species – 15.2%) endemic to Turkey, yielding a total herpetofaunal endemism of 18.9%. While 38 species have not been threat-assessed by the IUCN, 92 of the 180 Turkish herpetofaunal species are of Least Concern (LC), 13 are Near Threatened (NT), 10 are Vulnerable (VU), 14 are Endangered (EN), and 7 are Critically Endangered (CR). In addition, 6 species are in the DD (Data Deficient) category.

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

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The analysis of a 581 bp section of the nuclear gene c-mos revealed multiple copies of putative functional sequences as well as pseudogenes in three closely related lacertid species Lacerta laevis, L. kulzeri and L. cyanisparsa. A phylogenetic analysis of c-mos in comparison with a molecular phylogeny based on the mitochondrial cytochrome b gene supports our findings. The study also provides new insights into the phylogenetic relationships of L. cyanisparsa and L. laevis. Pseudogenes of the three species share 11 single-nucleotide substitutions, a 1 bp deletion and a premature stop codon but differ by group-specific mutations. This result suggests that the c-mos gene has become duplicated and subsequently silenced already in the common ancestor of the three species. Sequence divergence suggests that the duplication and the loss of function occurred in the late Miocene/early Pliocene, i.e., about 5 million years ago. Indications of gene conversion are discussed. We suggest that future studies using c-mos for phylogenetic studies should provide evidence for the orthology of the sequences compared.

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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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Revision of the Levantine Lacerta laevis / kulzeri complex: 1. The saxicolous lizard Lacerta cyanisparsa sp.n. The probably allopatric new species belongs to the Levantine Lacerta laevis/kulzeri complex. Morphologically, it has an intermediate position. The Syrian and Turkish populations can be distinguished by pholidosis. Like L . kulzeri s.l., it is a saxicolous lizard. It lives in the northern parts of the Inner Levant , i.e. east of the Syrian rift valley in NW Syria and adjacent Turkey. Its habitats and ecological affinities with the syntopic L . cappadocica wolteri, are described. Data on courtship behaviour are given.

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In this study, it was aimed to determine the amphibian and reptile species distributed in Kahramanmaraş province. Between the years 2016-2018, a total of 52 species (6 amphibians, 4 turtles, 21 lizards and 21 snakes species) belonging to 20 families were determined in Kahramanmaraş province during field surveys conducted at 451 localities. The records and their locations are presented in a map and a table. However, Bufo bufo (Linnaeus, 1758), Darevskia valentini (Boettger, 1892), Ablepharus chernovi Darevsky, 1953, Chamaeleo chamaeleon (Linnaeus, 1758), Parvilacerta parva (Boulenger, 1887), Anatololacerta pelasgiana (Mertens, 1959), Elaphe sauromates (Pallas, 1811) and Rhynchocalamus satunini (Nikolsky, 1899) were recorded for the first time from Kahramanmaraş.

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Knowledge on the spatial distribution of taxa is crucial for the decision-making processes in conservation and management of biodiversity that rely on precise distribution data. We present an annotated list for a total of 37 amphibian (20 caudatans and 17 anurans) and 141 reptile species (11 chelonians, 70 lizards, 3 amphisbaenians and 57 snakes) in Turkey, using both available scientific literature up to December 2020 and our own fieldwork data from 1987 to 2020. We provide a comprehensive listing of taxonomy, names, distribution and conservation status of Turkish amphibians and reptiles. The herpetofauna list will be particularly useful for establishing national conservation priorities as well as for placing Turkish fauna into phylogenetic and biogeographic contexts. We compiled information published in books, journals and various web sources and added our personal data. We projected the data in the WGS84 coordinate system and created an overlay grid with cells of 50x50 km2. The database comprises more than 500 grid cells and 11,913 records. As a result, the distribution of Turkish amphibians and reptiles has been extensively mapped with geographical information systems and a database has been created. The obtained data will be useful in planning future studies on taxonomy, ecology and conservation of Turkish amphibians and reptiles.

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The adult skeletons of lacertid lizards Phoenicolacerta laevis and P. cyanisparsa are described based on cleared-and-stained specimens. In comparison with each lacertid species, there are remarkable differences in both cranial and postcranial bones. These are the shape of some cranial bones such as the premaxilla, nasal, quadrate, squamosal, jugal and dentary and the shape of the ischium and ischio-pubis opening and the number of the last presacral vertebrae with small ribs for the postcranial skeletal elements. These detailed descriptions provide as a model to compare lacertid lizards and contribute to understand squamate osteology for further studies.