AG magazine (in print)
Online magazine (pdf)
Online articles (html)
Literature- and poster projects
of the real lizards, family Lacertidae
Podarcis melisellensis melisellensis (BRAUN, 1877)
Bischoff, W. (1973) -
Boulenger, G.A. (1920) -
Braun, M. (1877) -
Brecko, J. & Huyghe, K. & Vanhooydonck, B. & Herrel, A. & Grbac, I. & Van Damme, R. (2008) -
Within populations, individual animals may vary considerably in morphology and ecology. The degree to which variation in morphology is related to ecological variation within a population remains largely unexplored. We investigated whether variation in body size and shape among sexes and age classes of the lizard Podarcis melisellensis translates in differential whole-animal performance (sprint speed, bite force), escape and prey attack behaviour in the field, microhabitat use and diet. Male and female adult lizards differed significantly in body size and head and limb proportions. These morphological differences were reflected in differences in bite strength, but not in sprint speed. Accordingly, field measurements of escape behaviour and prey attack speed did not differ between the sexes, but males ate larger, harder and faster prey than females. In addition to differences in body size, juveniles diverged from adults in relative limb and head dimensions. These shape differences may explain the relatively high sprint and bite capacities of juvenile lizards. Ontogenetic variation in morphology and performance is strongly reflected in the behaviour and ecology in the field, with juveniles differing from adults in aspects of their microhabitat use, escape behaviour and diet.
Bressi, N. (1999) -
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.
Dely, O.G. & Stohl, G. (1982) -
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.
Galvagni, E. (1902) -
Gelineo, S. & Gelineo, A. (1955) -
Huyghe, K. & Breugelmans, K. & Small, M. & Tadic, Z. & Van Damme, R. & Vanhooydonck, B. & Backeljau, T. (2009) -
We describe polymerase chain reaction primers and amplification conditions for 13 highly polymorphic microsatellite DNA loci isolated from the Dalmatian wall lizard, Podarcis melisellensis. The number of alleles per locus ranged from 12 to 41, with levels of observed heterozygosity between 0.62 and 0.94. Most of these loci were successfully cross-amplified in the closely related species P. sicula, but levels of polymorphism were always lower.
Huyghe, K. & Herrel, A. & Adriaens, D. & Tadic, Z. & Van Damme, R. (2009) -
Males of the lizard Podarcis melisellensis occur in three distinct colours that differ in bite performance, with orange males biting harder than white or yellow ones. Differences in bite force among colour morphs are best explained by differences in head height, suggesting underlying variation in cranial shape and/or the size of the jaw adductors. To explore this issue further, we examined variation in cranial shape, using geometric morphometric techniques. Additionally, we quantified differences in jaw adductor muscle mass. No significant differences in size corrected head shape were found, although some shape trends could be detected between the colour morphs. Orange males have relatively larger jaw adductors than yellow males. Not only the mass of the external jaw adductors, but also that of the internal jaw adductors was greater for the orange morph. Data for other cranial muscles not related to biting suggest that this is not the consequence of an overall increase in robustness in orange individuals. These results suggest that differences in bite performance among morphs are caused specifically by an increase in the mass of the jaw adductor, which may be induced by differences in circulating hormone levels.
Huyghe, K. & Husak, J.F. & Herrel, A. & Tadic, Z. & Moore, I.T. & Van Damme, R. & Vanhooydonck, B. (2009) -
Species with alternative phenotypes offer unique opportunities to investigate hormone–behavior relationships. We investigated the relationships between testosterone, corticosterone, morphology, performance, and immunity in a population of lizards (Podarcis melisellensis) which exhibits a color polymorphism. Males occur in three different color morphs (white, yellow, orange), providing an opportunity to test the idea of morphs being alternative solutions to the evolutionary challenges posed on the link between hormones, morphology, performance, and immunity. Morphs differed in bite force capacity, with orange males biting harder, and in corticosterone levels, with yellow males having lower levels than orange. However, morphs did not differ in testosterone levels or in the immunological parameters tested. At the individual level, across morphs, testosterone levels predicted size-corrected bite force capacity, but no relation was found between hormone levels and immunity. Our results do not support the testosterone-based polymorphism hypothesis and reject the hypothesis of a trade-off between testosterone and immunity in this species, but provide a mechanistic link between testosterone and a sexually selected performance trait.
Huyghe, K. & Small, M. & Vanhooydonck, B. & Herrel, A. & Tadic, Z. & Van Damme, R. & Backeljau, T. (2010) -
If alternative phenotypes in polymorphic populations do not mate randomly, they can be used as model systems to study adaptive diversification and possibly the early stages of sympatric speciation. In this case, non random mating is expected to support genetic divergence among the different phenotypes. In the present study, we use population genetic analyses to test putatively neutral genetic divergence (of microsatellite loci) among three colour morphs of the lizard Podarcis melisellensis, which is associated with differences in male morphology, performance and behaviour. We found weak evidence of genetic divergence, indicating that gene flow is somewhat restricted among morphs and suggesting possible adaptive diversification.
Huyghe, K. & Vanhooydonck, B. & Herrel, A. & Tadic, Z. & Van Damme, R. (2007) -
Males of a Croatian population of the lacertid lizard Podarcis melisellensis exhibit a striking polymorphism, with coloration of the throat and abdomen ranging from completely white, to yellow or orange. In a first attempt to explore the potential ecological and evolutionary significance of this polymorphism, we compared the three forms of males in aspects of their morphology, whole-animal performance, behavior, and ecology. Orange males are, on average, larger in snout-vent length and have disproportionately larger heads than either white or yellow males. This is reflected in orange males having higher bite force capacity and theoretically an increased access to harder prey. Residual limb length, maximal sprint speed and maximal exertion do not differ among color morphs. Body temperatures in the field are similar in the three morphs, but yellow males are caught at sites with slightly higher air temperatures than are orange and white males. Behavioral observations show no differences in time budgets or in the timing of activities among morphs. Microhabitat use is also similar in the three color morphs, but orange males were more often initially seen on rocky substrates. Our findings suggest that the observed polymorphism likely does not originate from a divergence in niche or use of resources, but possibly reflects an underlying polymorphism in mating tactics.
Jelić, D. & Karaica, B. & Koren, T. & Sterijovski, B. & Dragičević,P. & Podnar Lešić, M. & Kovač Konrad, P. & Treer, D. & Kuljerić, M. & Peranić, I. (2015) -
Jelić, D. & Kuljerić, M. & Koren, T. & Treer, D. & Šalamon, D. & Lončar, M. & Podnar Lešić, M. & Janev Hutinec, B. & Bogdanović, T. & Mekinić, S. & Jelić, K. (2012) -
Jelic, D. & Kuljeric, M. & Koren, T. & Treer, D. & Salomon, D. & Loncar, M. & Podnar Lesic, M. & Hutinec, B.J. & Bogdanovic, T. & Mekinic, S. & Jelic, K. (2012) -
Klemmer, K. (1957) -
Mertens, R. (1924) -
Nikolsky, A.M. (1915) -
Podnar, M. & Mayer, W. & Tvrftkovic, N. (2004) -
A 903 bp section of the mitochondrial cytochrome b gene was sequenced from 73 specimens of Podarcis melisellensis collected at 52 localities distributed over the major part of the species´ range. In addition, parts of the 12S (about 470 bp) and 16S rRNA (about 500 bp) genes were analysed for 11 representative samples leading to a congruent phylogeny. Our study includes representatives of all 20 subspecies recognized today. The phylogenetic analysis of the sequence data revealed three main clades: mainland with nearby islands, Vis archipelago, and Lastovo archipelago. The degree of mitochondrial DNA divergence among these clades suggests a separation of the respective population groups during the earliest Pleistocene. The phylogenetic pattern observed within the species is in sharp contrast to the actual taxonomic division into subspecies. A correlation between genetic diversity of P. melisellensis populations and paleogeography of the regions they inhabit is discussed.
Radovanović, M. (1937) -
Radovanović, M. (1941) -
Radovanović, M. (1956) -
Scherer, J. (1904) -
Vervust, B. & Grbac, I. & Brečko, J. Tvrtković, N. & Van Damme, R. (2009) -
In this paper we examine the distribution of amphibians and reptiles over the islands of the newly founded Lastovo Archipelago Nature Park (Lastovsko oto~je), Croatia. On several field trips between 1996 and 2008, we encountered five species of lizards (Podarcis sicula, P. melisellensis, Dalmatolacerta oxycephala, Hemidactylus turcicus and Pseudopus apodus), one species of snake (Dolichophis caspius), one species of sea turtle (Caretta caretta) and one species of toad (Bufo viridis). We confirm literature data on the presence of some of these species on different islands of the archipelago, and add distributional records for several other islands and islets. Logistic regression analyses show that the variables predicting presence/absence from different islands vary among species. Within species, populations from different islands noticeably vary in body size and shape, scalation, dorsal and ventral coloration, behaviour and density. This observation adds to the value of the study area as a »natural laboratory« for future research into the ecology and evolution of island populations. Although most species seem to be doing well presently, we list a number of possible hazards and concerns.
Werner, F. (1891) -
Werner, F. (1908) -
Wettstein, O. (1926) -