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In this article an introduction is given on the geological history leading to the separation of Podarcis lilfordi (GÜNTHER, 1874) and Podarcis pityusensis (BOSCÁ, 1883) as separate species, as well as a Holocene sea level rise model which combined with bathymetric data leads to an estimation of recent divergence time in populations of the Balearic lizards.

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New data on estimated divergence times of the populations of lacertid lizards in the Balearic Islands are provided in this second update of the October 2011 article: Estimating recent divergence time in populations of Podarcis lilfordi (GÜNTHER, 1874) and Podarcis pityusensis (BOSCÁ, 1883) (VAN DEN BERG 2011), which received its first update May 2012. In most cases better estimations of divergence times were available by using the NAVIONICS SonarCharts™webapp.

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This is our fifth report in a series on our whereabouts while collecting data for a future revision of the present subspecific order of the endemic Balearic sisterspecies Podarcis lilfordi (GÜNTHER, 1874) and Podarcis pityusensis (BOSCÁ, 1883), which data are stored in our free accessible database at www.pityusensis.nl (VAN DEN BERG & ZAWADZKI 2011 ; VAN DEN BERG et al. 2013 ; VAN DEN BERG et al. 2014a ; VAN DEN BERG et al. 2014b). During this trip from the 9th of May until the 23rd of May 2015, we were able to collect data on a few mainland Ibiza locations, as well as the following adjacent islands: Punta Galera, Es Canaret, Illa de la Xanga (Sal Rossa), Pouet de Ses Illetes, Formentera, Purroig, Es Vedrà, Rates, Malví Pla (North), Malví Rodó (South), S’Espardell, Calders, Penjats and Ses Margalides. We continue with the ventral coloration as a possible determining key as introduced in our 2014 trip report (VAN DEN BERG et al. 2014b). Images of the anal shields are presented of each lizard for purposes of illustration.

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EL ESTUDIO ABORDADO EN LA TESIS VERSA SOBRE LA CARACTERIZACION TAXONOMICA DE LA LAGARTIJA DE LAS PITIUSAS PODARCIS PITVUSENSIS. SE ANALIZAN LAS DISTINTAS POBLACIONES DESDE TRES ASPECTOS DISTINTOS: EL ANALISISBIOMETRICO EL ANALISIS ELECTROFORETICO DE DISTINTAS PROTEINAS Y EL ANALISIS COLORIMETRICO. LOS ANALISIS ESTADISTICOS APLICADOS SOBRE LAS VARIANTES BIOMETRICAS DEMUESTRAN LA EXISTENCIA DE DIVERSOS GRUPOS DE POBLACIONES MUY SEMEJANTES ENTRE SI. LA VARIABILIDAD DE LA ESPECIE NO SOLO ES FENOTIPICA SINO QUE TAMBIEN ES GENETICA DETECTANDOSE UNA DIVERSIDAD EN ESTOS CARACTERES SUPERIOR A LA ESPERADA EN REPTILES. SE OBSERVA UNA ALTA HETEROSIS QUE ES CARACTERISTICA DE LA ESPECIE LO QUE PARECE DEMOSTRAR QUE ESTA SE ENCUENTRA EN LAS PRIMERAS FASES DE COLONIZACIONY ADAPTACION A LOS DIFERENTES HABITATS OFRECEN LAS ISLAS QUE OCUPA. SE CONSTATA LA ACCION DEL EFECTO FUNDADOR Y LA DERIVA GENETICA EN LOS TRES ASPECTOS CONSIDERADOS EN LA TESIS ASI COMO UNA TENDENCIA EVOLUTIVA HACIA EL AUMENTO DE TAMAÑO SIEMPRE QUE NO EXISTA UNA PRESION SELECTIVA CONTRARIA. SUCEDE LO MISMO CON EL MELANISMO. CONSIDERANDO EL ESTADO EVOLUTIVO ACTUAL DE LA ESPECIE REFLEJADO EN LA PLASTICIDAD DE LAS DISTINTAS POBLACIONES DE ESTALAARTIJA Y EN LA ADAPTACION QUE MANIFIESTAN EN CADA NICHO CONCRETO ASI COMO EL CONCEPTO RESTRICTIVO ACTUAL DE SUBESPECIE LA AUTORA CONSIDERA QUE SOLO PUEDEN CONSIDERARSE SEIS TAXONES SUBESPECIFICOS O SUBESPECIES DE LA LAGARTIJA DE LAS PITIUSAS.

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In this paper are presented the results obtained with 45 populations of Podarcis pityusensis. Several multivariant technics are performed: discriminant analysis, cluster analysis and canonic analysis of populations. These populations present gradual change in all their biometric characteristics, and also a great interpopulation variability, that invalidate th statistical methods to discriminate between all of them. In different analysis very related population groups are found, that suggests they are constitute the same subspecies, in the actual taxonomic sense. These groups always inhabits islands with the same geological age, it is therefore necessary to complete the study with othr biological reflections, all of which are getting ready.

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The dorsal, side and belly colours of 118 specimens of Podarcis pityusensis have been analysed with physical methods. Twenty samples from 16 islands have been chosen, 3 of then from Eivissa Island (Ibiza), 2 from Formentera Island and 2 from Espardell Island. The results reveal great colouration differences between the same island samples and sometimes similar colouration between different islands (different subspecies). specimens. This feature seems to show the colour criteria is not useful in taxonomic subjects for this species.

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The variation in morphological and colouring features shown by the insular lacertid populations of Podarcis pityusensis is discussed from the point of view of their adaptive advantages to specific insular ecosystems. Insularity factors, i.e. area and island-age, have been found to be related to average body size, and the average luminosity of each population. Populations tend to show a size increase, a greater morphological homogeneity and darker dorsal colouring on smaller and older islands. Genetic drift seems to play a secondary role, whereas a positive selection in favour of melanism and giantism is observed. Both features are not linked as cause and effect, but seem to share a common cause: isolation and time enough to allow selection to take place. Predation, though slight in degree, does exist, and seems to be one of the selective pressure favouring melanism, together with the parallel trend towards an increase in body size and the need to an effective thermoregulation during the early hours of the day.

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The Ibiza wall lizard is the symbol of the Pityusic-Archipelago, but what makes this colorful reptile so special? The Symbol: wall lizards of Ibiza and Formentera will take you on a journey into the culture, biology, ecology, and conservation of Ibiza and Formentera’s most iconic animal.

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

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An electrophoretic comparison of ten colonies of Podarcis pityusensis Bosca, 1882 (Lacertidae) from Ibiza, Formentera and neighbouring islets (Balearic Is., Spain). 71 animals from ten colonies (vide list in text) of the Ibiza wall lizard Podarcis pi- tyusensis Bosca, 1882 were analysed by electrophoresis, on 12 % starch gel, and 16 gene- tic loci were studied, by checking against samples of Podarcis muralis muralis. The genetic frequency resulting in NEI`s identity index (I), reveals no clear differen- ces between the various colonies. However, itcan be seen on the resultant dendogram that P. p. carlkochi (affinis group) is distinct from the pityusensis sensu stricto group colonies. By other means we found characteristic allels for Podarcis pityusensis in four loci: GOT-1, IDM-1, G-6-PD-2 and 6-PGD, which differed from Podarcis muralis allels.

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The status of the populations of Podarcis pityusensis on about 70 islets and small islands around Ibiza and Formentera (Balearic Islands) is examined, using data from our own observations, and, to a lesser amount, other publications. Lizard populations were found on 43 islets, but data are lacking for another 13. Only 10 sites (18 %) have abundant and well-maintained populations. In 13 localities (23%), there is no geographic isolation between the populations, or this isolation is very poor and incomplete. The high probability of populations mixing, or actual observation of this mixing, in 19 islands (34%) is indicated. Human pressure on lizard populations is strong in 14 cases (25 %). And finally, 18 populations (about one third) may be considered highly endangered or already extinct by elimination or genetic mixing with other populations. Among the subspecies which became extinct through mixing are P.p. miguelensis, P.p. subformenterae, P.p. algae, P.p. sabinae and P.p. grueni. The need for adequate protective measures aimed at the conservation of the remaining populations is emphasized.

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While the use of faecal pellets is widely accepted as a primary methodological source of data for dietary studies, a recent paper advocated for the use of gut contents. This was due to the fact that faecal samples would give biased results of the diet of arthropod predators, due to a lower representation of soft-bodied prey in faecal pellets. To test this assumption, we compared the spring diet of several populations of two insular lizards from the Balearic Islands (Spain), Podarcis lilfordi and Podarcis pityusensis, using both faecal pellets and gut contents. Our results do not support the supposed bias of dietary analyses based on faecal pellets. Indeed, soft-bodied prey and particularly insect larvae are often equally represented in faecal pellets and gut contents. Alternatively, soft bodied prey are represented in different proportions in gut contents and faecal pellets, but in some cases with higher proportions being observed in the gut contents, and in other cases with higher proportions in faecal samples. We conclude that faecal pellets can be a reliable source of information for dietary studies.

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The parasitic female of the nematode Strongyloides ophiusensis sp. n.. fund in the intestine of lizard Podarcis pityusensis (Bosca, 1883) from Balearic Islands (West Mediterranean), is described. This species differs from other similar Strongyloides species in the body size, the morphology of the stoma, the structure of the ovaries and in the stage of development of the eggs, and also in some ecological and chorological characters.

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The knowledge of the helminth communities of reptiles and their ecological relationships with their hosts are until the present not well known. Some general researches have been made only on American herps (AHO 1990). Recently, ROCA & HORNERO (1991a, 1991b) attempted similar kind of researches from Mediter- ranean insularlizards.

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Two monophyletic sister species of wall lizards inhabit the two main groups of Balearic Islands: Podarcis lilfordi from islets and small islands around Mallorca and Menorca and Podarcis pityusensis from Ibiza, Formentera and associated islets. Genetic diversity within the endangered P. lilfordi has been well characterized, but P. pityusensis has not been studied in depth. Here, 2430 bp of mtDNA and 15 microsatellite loci were analysed from P. pityusensis populations from across its natural range. Two main genetic groupings were identified, although geographical structuring differed slightly between the mtDNA and the nuclear loci. In general, individuals from islets/islands adjacent to the main island of Ibiza were genetically distinct from those from Formentera and the associated Freus islands for both mtDNA and the nuclear loci. However, most individuals from the island of Ibiza were grouped with neighbouring islets/islands for nuclear loci, but with Formentera and Freus islands for the mitochondrial locus. A time-calibrated Bayesian tree was constructed for the principal mitochondrial lineages within the Balearics, using the multispecies coalescent model, and provided statistical support for divergence of the two main P. pityusensis lineages 0.111–0.295 Ma. This suggests a mid-late Pleistocene intraspecific divergence, compared with an early Pleistocene divergence in P. lilfordi, and postdates some major increases in sea level between 0.4 and 0.6 Ma, which may have flooded Formentera. The program IMa2 provided a posterior divergence time of 0.089–0.221 Ma, which was similar to the multispecies coalescent tree estimate. More significantly, it indicated low but asymmetric effective gene copy migration rates, with higher migration from Formentera to Ibiza populations. Our findings suggest that much of the present-day diversity may have originated from a late Pleistocene colonization of one island group from the other, followed by allopatric divergence of these populations. Subsequent gene flow between these insular groups seems likely to be explained by recent human introductions. Two evolutionary significant units can be defined for P. pityusensis but these units would need to exclude the populations that have been the subjects of recent admixture.