Podarcis muralis

Superregnum: Eukaryota
Cladus: Unikonta
Cladus: Opisthokonta
Cladus: Holozoa
Regnum: Animalia
Subregnum: Eumetazoa
Cladus: Bilateria
Cladus: Nephrozoa
Superphylum: Deuterostomia
Phylum: Chordata
Subphylum: Vertebrata
Infraphylum: Gnathostomata
Megaclassis: Osteichthyes
Cladus: Sarcopterygii
Cladus: Rhipidistia
Cladus: Tetrapodomorpha
Cladus: Eotetrapodiformes
Cladus: Elpistostegalia
Superclassis: Tetrapoda
Cladus: Reptiliomorpha
Cladus: Amniota
Classis: Reptilia
Cladus: Eureptilia
Cladus: Romeriida
Subclassis: Diapsida
Cladus: Sauria
Infraclassis: Lepidosauromorpha
Superordo: Lepidosauria
Ordo: Squamata
Cladus: Unidentata Episquamata

Subordo: Lacertoidea
Infraordo: Lacertibaenia

Familia: Lacertidae
Subfamilia: Lacertinae
Genus: Podarcis
Species: Podarcis muralis
Subspecies (13): P. m. albanica – P. m. appenninica – P. m. baldasseronii – P. m. beccarii – P. m. breviceps – P. m. brongniardii – P. m. colosii – P. m. maculiventris – P. m. marcuccii – P. m. muralis – P. m. nigriventris – P. m. sammichelii – P. m. tinettoi
Name

Podarcis muralis (Laurenti, 1768)

Type locality: unknown.
Combinations

Seps muralis Laurenti, 1768: 61 [original combination]
Lacerta muralis — Lichtenstein, 1823: 92 [subsequent combination]
Podarcis muralis — Wagler, 1830: 155 [subsequent combination]

References
Primary references

Laurenti, J.N. 1768. Specimen medicum, exhibens synopsin reptilium emendatam cum experimentis circa venena et antidota reptilium austracorum, quod authoritate et consensu (In Latin). Joan Thomae: Vienna. 217 pp. BHL Reference page.

Links

Uetz, P. & Hallermann, J. 2022. Podarcis muralis. The Reptile Database. Accessed on 24 January 2019.
Böhme, W., Pérez-Mellado, V., Cheylan, M., Nettmann, H.C., Krecsák, L., Sterijovski, B., Schmidt, B., Lymberakis, P., Podloucky, R., Sindaco, R. & Avci, A. 2009. IUCN: Podarcis muralis (Least Concern). The IUCN Red List of Threatened Species 2009: e.T61550A12514105. DOI: 10.2305/IUCN.UK.2009.RLTS.T61550A12514105.en

Vernacular names
Boarisch: Hegedechs
български: Стенен гущер
brezhoneg: Glazard ar mogerioù
català: Sargantana roquera
čeština: Ještěrka zední
Deutsch: Mauereidechse
Ελληνικά : Τοιχόσαυρα
English: Wall lizard
español: Lagartija roquera
euskara: Horma-sugandila
français: Lézard des murailles
galego: lagartixa dos muros
हिन्दी: छिपकली
magyar: Fali gyík
italiano: Podarcis muralis
Nederlands: Muurhagedis
polski: Jaszczurka murowa
português: Lagartixa dos muros
Runa Simi: Pirqa allallanka
slovenčina: Jašterica múrová
slovenščina: Pozidna kuščarica
српски / srpski: Зидни гуштер
svenska: Murödla

Podarcis muralis (common wall lizard) is a species of lizard with a large distribution in Europe and well-established introduced populations in North America, where it is also called the European wall lizard. It can grow to about 20 cm (7.9 in) in total length.

Description

The common wall lizard is a small, thin lizard whose small scales are highly variable in colour and pattern. Its coloration is generally brownish or greyish, and may occasionally be tinged with green. In some individuals, the row of spots along their backs may form a line, while others may have a reticulated pattern with dark spots on the side and scattered white spots that can be blue in the shoulder region. The tail is brown, grey or rust in colour, and may also have light bars on the sides. The belly region has six rows of larger rectangular scales that are generally reddish, pink, or orangish. Common wall lizards may also have dark markings on the throat. This lizard has six distinct morphological forms[3] which are identified by the colouration of its throat and underbelly. Three of these are pure morphs consisting only of solid colours on their scales: white, red (orange) or yellow, and three other morphs are distinguished by a combination of colours: white-yellow, white-red and yellow-red.[3]
Ecology

The common wall lizard prefers rocky environments, including urban settings, where it can scurry between rock, rubble, debris and buildings. In the southern part of its range it tends to occur in humid or semi-humid habitats, compared to drier habitats in the north.[1][4]
Chemical communication

Common wall lizards rely both on visual and chemical signals to communicate with conspecifics.[5][6][7] Male wall lizards are equipped with femoral glands, which produce a waxy secretion used for chemical signalling.[8][9] Both the proteinic and lipophilic compounds in the secretions are known to carry socially relevant information.[10][11]
Polymorphism

The six morphs of this lizard are primarily identifiable by colour and can be distinguished with the naked eye. However, they are commonly confirmed by digital photo and colour analysis.[3] Source of colouration comes from different pigments within the lizard, with yellow colouration originating from carotenoids, and the expression of red/orange colour from pteridines.[12] This is indicative that a phenomenon such as multiple alleles or epistasis may have a role in determining morphology. Morphs also differ in aspects other than colouration: differences between morphs are seen with femoral gland secretion, immune competence and body size.[13] For males, colouration is visible on the underbelly, but in females of all the morphs there is less colouration seen in this region, indicating that sexual dimorphism occurs within this species.[3]
Variations between morphs

Aside from differences in colour, the morphs vary by length, survival rate, and immune resistance/response to infection.[13]
Podarcis muralis photographed at Mosel valley (Germany)

Susceptibility to infection also varies between morphs, red and yellow-red morphs are the most susceptible to infection by the haemogregarine parasite, a common parasite for these lizards. White morphs are the most resistant to this parasite and the yellow morphs are at an intermediate value of immune resistance and intensity.[13] Certain traits can also lead to a variation in snout-vent length in each of these morphs.[13] For example, in orange morphs, sexual selection favours larger morphs which makes them, on average, larger than the other morphs.[13]

The femoral gland secretions of males differ in chemical composition according to each respective morph.[14] Secretions are used by males for intra-species communication, such as marking of territories and attracting potential mates. Individuals share the same organics within the secretions, but the concentrations of certain key compounds differ. For example, α-tocopherol is present in higher concentrations in the secretions of red morphs.[14] This molecule allows for scents to remain in the environment longer by reducing the rate of oxidation in humid environments.[15] This indicates that red morphs tend to be more territorial and maintain territories for longer periods of time compared to other morphs. This phenomenon is also seen when it comes to the age of lizards. Similarly, older, more territorial lizards have higher levels of α-tocopherol compared to younger individuals who are more prone to roaming regardless of morph.[14] Again, indicating that the composition of the secretions relate to the function. Furanones are found in higher concentrations in white morphs, followed by yellow, then red morphs.[14]

Among females, reproductive strategies differ by morph; yellow females are r strategists, producing many smaller eggs in their clutch which would allow for numerous offspring to be produced and proliferate in smaller populations with less competition.[16] White females are K strategists, producing fewer, larger eggs which makes offspring more likely to survive in harsher, more competitive environments.[16] Red females can be r or K strategists based on the environment they are in.[16] The existence of alternate strategies points to how morphs have adapted to different environments and hints to the maintenance of colour polymorphism as with fluctuations in environments each morph will eventually be the fittest and as such will not be selected out of the population.

The differences observed between morphs are unique evolutionary trade offs employed by each morph to promote survival within the different environments they face in light of limited ability to adapt perfectly to each pressure. Such a trade off is seen when comparing orange morphs to white morphs: morphs, on average, have larger body sizes compared to the white morphs but, in exchange, they are more prone to parasitic infection.[13] In orange morphs, more emphasis is placed on being larger and having the ability to physically compete and ward of potential threats, but in white morphs, metabolic emphasis is placed on having a more hardy immune system to resist infection. Again, these trade offs can arise as there are selective differences in the environment each morph prefers. The differences in the relative proportions of the morphs with respect to location show that environmental pressures differ and some morphs' trade offs are more successful in specific environments than another's.[3]
Distribution and status

The natural range spans much of the mainland Europe except from the north and very south and extends to Turkey.[1][4] It occurs as introduced populations in southern Britain,[1][17] where one such population in the seaside town of Ventnor on the Isle of Wight has become somewhat famous, and also in North America.[1] There has been some scientific debate as to whether the populations in Southern England represent the northern edge of their native range.[18]
North America

Podarcis muralis has been introduced in the United States and is spreading throughout the Cincinnati metropolitan area. It is commonly observed living in limestone outcrops, rock walls, and rubble along the Ohio River basin.[19]
Podarcis muralis photographed in Cincinnati, Ohio - 2015.

It is referred to locally in the Cincinnati/Northern Kentucky area as the "Lazarus lizard",[20] as it was introduced to the area around 1950 by George Rau, a boy who was a member of the family who owned the Lazarus department store chain (now absorbed into Macy's). After he returned from a family vacation to northern Italy, he released about 10 of the reptiles near his Cincinnati home.[21] Genetic testing has revealed that as little as only three of these lizards survived long enough to reproduce, meaning they were subject to an extreme genetic bottleneck.[22] This prolific lizard has reproduced exponentially; it continues to expand its distribution range annually, and has established itself so well in southwest Ohio, it is now considered a naturalized species by the Ohio Department of Natural Resources and is protected under state law (it is illegal to harm, capture, or possess this animal without a proper licence).[23]

Besides Ohio, P. muralis has also been introduced in other U.S. states. Populations occur in Kenton and Campbell counties in Kentucky, and in parts of Indiana.

The European wall lizard was also introduced to Vancouver Island, British Columbia, Canada in 1970, when a dozen individuals were released into the wild from a small private zoo.[24]

This lizard is also present in Los Angeles and San Diego counties in California and may exist elsewhere in California.
See also

List of reptiles of Italy
List of reptiles of Spain
List of reptiles of Canada

References

Wolfgang Böhme, Valentin Pérez-Mellado, Marc Cheylan, Hans Konrad Nettmann, László Krecsák, Bogoljub Sterijovski, Benedikt Schmidt, Petros Lymberakis, Richard Podloucky, Roberto Sindaco, Aziz Avci (2009). "Podarcis muralis". IUCN Red List of Threatened Species. 2009: e.T61550A12514105. doi:10.2305/IUCN.UK.2009.RLTS.T61550A12514105.en. Retrieved 19 November 2021.
P. Uetz (ed.). "Podarcis muralis (Laurenti, 1768)". The Reptile Database. Retrieved May 9, 2012.
Sacchi, Roberto; et al. (4 June 2013). "Colour variation in the polymorphic common wall lizard (Podarcis muralis): An analysis using the RGB colour system". Zoologischer Anzeiger. 252 (4): 431–439. doi:10.1016/j.jcz.2013.03.001.
Arnold, Nicholas; Ovenden, Denys (2002). A field guide to the reptiles and amphibians of Britain and Europe (2nd ed.). London: HarperCollins. pp. 145–147. ISBN 9780002199643.
Pérez i de Lanuza, Guillem; Carazo, Pau; Font, Enrique (2014-04-01). "Colours of quality: structural (but not pigment) coloration informs about male quality in a polychromatic lizard". Animal Behaviour. 90: 73–81. doi:10.1016/j.anbehav.2014.01.017. ISSN 0003-3472. S2CID 53150641.
Font, Enrique; Carazo, Pau; Pérez i de Lanuza, Guillem; Kramer, Matthew (2012). "Predator-elicited foot shakes in wall lizards (Podarcis muralis): Evidence for a pursuit-deterrent function". Journal of Comparative Psychology. 126 (1): 87–96. doi:10.1037/a0025446. ISSN 1939-2087. PMID 22352886.
Font, Enrique; Barbosa, Diana; Sampedro, Carlos; Carazo, Pau (May 2012). "Social behavior, chemical communication, and adult neurogenesis: Studies of scent mark function in Podarcis wall lizards". General and Comparative Endocrinology. 177 (1): 9–17. doi:10.1016/j.ygcen.2012.02.015. PMID 22406138.
Heathcote, Robert J. P.; Bell, Emily; d’Ettorre, Patrizia; While, Geoffrey M.; Uller, Tobias (May 2014). "The scent of sun worship: basking experience alters scent mark composition in male lizards". Behavioral Ecology and Sociobiology. 68 (5): 861–870. doi:10.1007/s00265-014-1700-4. ISSN 0340-5443. S2CID 16917937.
MacGregor, Hannah E. A.; Lewandowsky, Rachel A. M.; d'Ettorre, Patrizia; Leroy, Chloé; Davies, Noel W.; While, Geoffrey M.; Uller, Tobias (October 2017). "Chemical communication, sexual selection, and introgression in wall lizards: CHEMICAL INTROGRESSION IN WALL LIZARDS". Evolution. 71 (10): 2327–2343. doi:10.1111/evo.13317. PMID 28745028. S2CID 3459975.
Mangiacotti, Marco; Gaggiani, Sofia; Coladonato, Alan Jioele; Scali, Stefano; Zuffi, Marco Alberto Luca; Sacchi, Roberto (February 2019). "First experimental evidence that proteins from femoral glands convey identity-related information in a lizard". Acta Ethologica. 22 (1): 57–65. doi:10.1007/s10211-018-00307-1. ISSN 0873-9749. S2CID 57425673.
Mangiacotti, Marco; Fumagalli, Marco; Cagnone, Maddalena; Viglio, Simona; Bardoni, Anna Maria; Scali, Stefano; Sacchi, Roberto (December 2019). "Morph-specific protein patterns in the femoral gland secretions of a colour polymorphic lizard". Scientific Reports. 9 (1): 8412. Bibcode:2019NatSR...9.8412M. doi:10.1038/s41598-019-44889-7. ISSN 2045-2322. PMC 6557888. PMID 31182789.
Bagnara, Joseph (1 July 1968). "The Dermal Chromatophore Unit". Journal of Cell Biology. 38 (1): 67–79. doi:10.1083/jcb.38.1.67. PMC 2107474. PMID 5691979.
Calsbeek, B (6 April 2010). "Multivariate phenotypes and the potential for alternative phenotypic optima in wall lizard (Podarcis muralis) ventral colour morphs". Journal of Evolutionary Biology. 23 (6): 1138–1147. doi:10.1111/j.1420-9101.2010.01978.x. PMID 20406342. S2CID 40392562.
Pellitteri-Rosa, D. (5 February 2014). "Chemical polymorphism in male femoral gland secretions matches polymorphic coloration in common wall lizards (Podarcis muralis)". Chemoecology. 24 (2): 67–78. doi:10.1007/s00049-014-0148-3. S2CID 18390221.
Kopena, Renata (27 February 2009). "Lipophlic compounds from the femoral gland secretions of male Hungarian green lizards, Lacerta viridis" (PDF). Zeitschrift für Naturforschung. 64 (5–6): 434–440. doi:10.1515/znc-2009-5-622. PMID 19678551. S2CID 17255038. Retrieved 20 October 2015.
Galeotti, Paleo (6 January 2013). "Colour polymorphism and alternative breeding strategies: effects of parent's colour morph on fitness traits in the common wall lizard". Evolutionary Biology. 40 (3): 385–394. doi:10.1007/s11692-012-9222-3. S2CID 1729020.
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"4-inch-long visitors liked Cincinnati so much, they stayed". Cincinnati Business Courier. Nov 10, 2003. Retrieved 9 October 2015.
Dennis, Spencer (May 23, 2011). "Lazarus lizards now part of our culture". Archived from the original on May 25, 2011. Retrieved May 26, 2011.
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"Bottlenecks and Microhabitat Preference in Invasive Wall Lizard, Podarcis muralis". Master's thesis, University of Cincinnati – via OhioLINK Electronic Theses and Dissertations Center.
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