Age and growth of the common wall lizard, Podarcis muralis (Laurenti, 1768)

in Animal Biology
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The present study was designed to compare the life history traits of two Podarcis muralis populations located at sites of different elevation. The age at maturity was similar in both populations, whereas longevity was found to be lower in the lowland one (Dereköy). The males and females of both populations had a similar snout-vent length (SVL) and mean age. Sexual size dimorphism (SSD) was weak in the highland population, males being slightly larger than females, whereas a strong male-biased SSD was observed in the lowland one. The growth coefficient (k) and growth rates were similar in both populations. This study indicates that the age at maturation (2-3 years) and growth rates (2.37 mm/year) are similar in two populations of P. muralis exposed to different climatic and environmental conditions. Longevity was slightly higher in the highland population (16 years) compared to the lowland one (14 years).

Age and growth of the common wall lizard, Podarcis muralis (Laurenti, 1768)

in Animal Biology



AdolphS.C. & PorterW.P. (1993) Temperature, activity, and lizard life histories. Am. Nat.142273-295.

AllanG.M.PrelypchanC.J. & GregoryP.T. (2006) Population profile of an introduced species, the common wall lizard (Podarcis muralis), on Vancouver Island, Canada. Can. J. Zool.8451-57.

AnderssonM. (1994) Sexual Selection. Princeton University PressPrinceton, NJ, USA.

AndrewsR.M. (1976) Growth rate in island and mainland anole lizards. Copeia1976477-482.

BallingerR.E. (1977) Reproductive strategies: food availability as a source of proximal variation in a lizard. Ecology58628-635.

BarbaultR. & MouY.-P. (1988) Population dynamics of the common wall lizard, Podarcis muralis, in southwestern France. Herpetologica4438-47.

BöhmeW.Pérez-MelladoV.CheylanM.NettmannH.K.KrecsákL.SterijovskiB.SchmidtB.LymberakisP.PodlouckyR.SindacoR. & AvciA. (2009) Podarcis muralis. .The IUCN Red List of Threatened Species 2009. Accessed on 17 February 2017.

BorettoJ.M.Cabezas-CartesF. & IbargüengoytíaN.R. (2015) Energy allocation to growth and reproduction in a viviparous lizard endemic to the highlands of the Andes, Argentina. J. Zool.29777-86.

BülbülU.KurnazM.EroğluA.İ.KoçH. & KutrupB. (2016a) Age and growth of the red-bellied lizard, Darevskia parvula. Anim. Biol.6681-95.

BülbülU.KurnazM.EroğluA.İ.KoçH. & KutrupB. (2016b) Body size and age structure of the endangered Clark’s lizard (Darevskia clarkorum) populations from two different altitudes in Turkey. Amphibia-Reptilia37450-456.

Cabezas-CartesF.BorettoJ.M. & IbargüengoytíaN.R. (2015) Age, growth and life-history parameters of an endemic vulnerable lizard from Patagonia, Argentina. Herpetol. J.25215-224.

CaleyM.J. & SchwarzkopfL. (2004) Complex growth rate evolution in a latitudinally widespread species. Evolution58862-869.

CastanetJ. (1994) Age estimation and longevity in reptiles. Gerontology40174-192.

CastanetJ. & RocheE. (1981) Détermination de l’âge chez le lézard des murailles, Lacerta muralis (Laurenti, 1768) au moyen de la squelettochronologie. Rev. Suisse Zool.88215-226.

CastanetJ. & SmirinaE.M. (1990) Introduction to the skeletochronological method in amphibians and reptiles. Ann. Sci. Nat. Zool.11191-196.

ChristianK.A. (1986) Physiological consequences of nightime temperature for a tropical herbivorous lizard (Cyciura nubila). Can. J. Zool.64836-840.

ConoverD.O.DuffyT.A. & HiceL.A. (2009) The covariance between genetic and environmental influences across ecological gradients: reassessing the evolutionary significance of countergradient and cogradient variation. Ann. NY Acad. Sci.1168100-129.

CoxR.M.SkellyS.L. & John-AlderH.B. (2003) A comparative test of adaptive hypotheses for sexual size dimorphism in lizards. Evolution571653-1669.

DunhamA.E. (1978) Food availability as a proximate factor influencing individual growth rates in the iguanid lizard Sceloporus merriami. Ecology59770-778.

DunhamA.E.GrantB.W. & OverallK.L. (1989) Interfaces between biophysical and physiological ecology and the population ecology of terrestrial vertebrate ectotherms. Phys. Zool.62335-355.

EroğluA.İ.BülbülU. & KurnazM. (2017a) Age structure and growth in a Turkish population of the Crimean wall lizard, Podarcis tauricus (Pallas, 1814) (Squamata: Sauria: Lacertidae). Herpetozoa29125-133.

Eroğlu A.İ.Bülbül U. & Kurnaz M. (2017b) Age structure and growth in a Turkish population of the Italian wall lizard Podarcis siculus (Rafinesque-Schmaltz, 1810) (Reptilia: Lacertidae). Acta Zool. Bulg.69209-214.

FairbairnD.J.BlanckenhornW.U. & SzekelyT. (2007) Sex Size and Gender Roles: Evolutionary Studies of Sexual Dimorphism. Oxford University PressOxford, UK.

FoxS.F. (1983) Fitness, home-range quality, and aggresion in Uta stansburiana. In: R.B. HueyE.R. Pianka & T.W. Schoener (Eds) Lizard Ecology: Studies of a Model Organism pp. 149-168. Harvard University PressCambridge, MA, USA.

GadgilM. & BossertW.H. (1970) Life historical consequences of natural selection. Am. Nat.1041-24.

GrantB.W. & DunhamA.E. (1988) Thermal imposed time constraints on the activity of the desert lizard Sceloporus merriami. Ecology69167-176.

GuarinoF.M.GiaI.D. & SindacoR. (2010) Age and growth of the sand lizards (Lacerta agilis) from a high alpine population of north-western Italy. Acta Herpetol.523-29.

GülS.ÖzdemirN.KumlutasY. & IlgazÇ. (2014) Age structure and body size in three populations of Darevskia rudis (Bedriaga, 1886) from different altitudes (Squamata: Sauria: Lacertidae). Herpetozoa26151-158.

GülS.ÖzdemirN.AvcıA.KumlutasY. & IlgazÇ. (2015) Altitudinal effects on the life history of the Anatolian lizard (Apathya cappadocica, Werner 1902) from southeastern Anatolia, Turkey. Turk. J. Zool.39507-512.

HallidayT.R. & VerrellP.A. (1988) Body size and age in amphibians and reptiles. J. Herpetol.22253-265.

HerrelA.MooreJ.A.BredewegE.M. & NelsonN.J. (2010) Sexual dimorphism, body size, bite force and male mating success in tuatara. Biol. J. Linn. Soc.100287-292.

In den BoschH.A.J. & BoutR.G. (1998) Relationships between maternal size, egg size, clutch size, and hatchling size in European lacertid lizards. J. Herpetol.32410-417.

JamesC.D. (1991) Growth rates and ages at maturity of sympatric scincid lizards (Ctenotus) in central Australia. J. Herpetol.25284-295.

JenssenT.A. & AndrewsR.M. (1984) Seasonal growth rates in the Jamaican lizard, Anolis opalinus. J. Herpetol.18338-341.

John-AlderH.B. & CoxR.M. (2007) The development of sexual size dimorphism in sceloporus lizards: testosterone as a bipotential growth regulator. In: D.J. FairbairnW.U. Blanckenhorn & T. Székely (Eds) Sex Size and Gender Roles: Evolutionary Studies of Sexual Size Dimorphism pp. 195-204. Oxford University PressLondon, UK.

KaliontzopoulouA.CarreteroM.A. & LlorenteG.A. (2007) Multivariate and geometric morphometrics in the analysis of sexual dimorphism variation in Podarcis lizards. J. Morph.268152-165.

KleinenbergS.E. & SmirinaE.M. (1969) On the method of determination of age in amphibians. Zool. Zh.481090-1094 [in Russian].

KolarovT.N.VljevicL.K.PolovicL.D.G. & KalezicM.L. (2010) The body size, age structure and growth pattern of the endemic Balkan mosor rock lizard (Dinolacerta mosorensis Kolombatovich, 1886). Acta Zool. Hung.5655-71.

Lemos-EspinalJ.A. & BallingerR.E. (1995) Ecology of growth of the high altitude lizard Sceloporus grammicus on the eastern slope of Iztaccihuatl Volcano, Puebla, Mexico. Trans. Nebraska Acad. Sci.2277-85.

LovichJ.E. & GibbonsJ.W. (1992) A review of techniques for quantifying sexual size dimorphism. Growth Dev. Aging56269-281.

LuH.L.XuC.X.JinY.T.Hero J.M. & DuW.G. (2017) Proximate causes of altitudinal differences in body size in an agamid lizard. Ecol. Evol.8645-654.

NewmanS.J. & DunkI.J. (2002) Growth, age validation, mortality, and other population characteristics of the red emperor snapper Lutjanus sebae (Cuvier, 1828), off the Kimberley Coast of north-western Australia. Estuar. Coast. Shelf Sci.5567-80.

OlssonM.ShineR.WapstraE.UjvariB. & MadsenT. (2002) Sexual dimorphism in lizard body shape: the roles of sexual selection and fecundity selection. Evolution561538-1542.

PiankaE.R. (1970) On r- and K-selection. Am. Nat.102592-597.

RahmanM.D.H. & TachiharaK. (2005) Age and growth of Sillago aeolus in Okinawa Island, Japan. J. Oceanogr.61569-573.

RoitbergE.S. & SmirinaE.M. (2006a) Adult body length and sexual size dimorphism in Lacerta agilis boemica (Reptilia, Lacertidae): between-year and interlocality variation. In: C. CortiP. Lo Cascio & M. Biaggini (Eds) Mainland and Insular Lacertid Lizards: a Mediterranean Perspective pp. 175-187. Firenze University PressFlorence, Italy.

RoitbergE.S. & SmirinaE.M. (2006b) Age, body size and growth of Lacerta agilis boemica and L. agilis strigata: a comparative study of two closely related lizard species based on skeletochronology. Herpetol. J.16133-148.

RyserJ. (1988) Determination of growth and maturation in the common frog, Rana temporaria, by skeletochronology. J. Zool. Lond.216673-685.

ShineR. & CharnovE.L. (1992) Patterns of survival, growth, and maturation in snakes and lizards. Am. Nat.1391257-1269.

SilleroN.CamposJ.BonardiA.CortiC.CreemersR.CrochetP.-A.IsailovicJ.C.DenoëlM.FicetolaG.F.GonçalvesJ.KuzminS.Lymberakis PousP.RodríguezA.SindacoR.SpeybroeckJ.ToxopeusB.VieitesD.R. & VencesM. (2014) Updated distribution and biogeography of amphibians and reptiles of Europe. Amphibia-Reptilia351-31.

SinschU. (2015) Skeletochronological assessment of demographic life-history traits in amphibians. Herpetol. J.255-13.

SinschU.Pelster B. & LudwigG. (2015) Large-scale variation of size- and age-related life-history traits in the common frog: a sensitive test case for macroecological rules. J. Zool.29732-43.

StrijboschH.BonnemayerJ.J.A.M. & DietvorstP.J.M. (1980) The northernmost population of Podarcis muralis (Lacertilia, Lacertidae). Amphibia-Reptilia1161-172.

TaoY.MingruC.JianguoD.ZhenbinL. & ShengyunY. (2012) Age and growth changes and population dynamics of the black pomfret (Parastromateus niger) and the frigate tuna (Auxis thazard thazard), in the Taiwan strait. Lat. Am. J. Aquat. Res.40649-656.

TinkleD.W.WilburA.M. & TilleyS.J. (1970) Evolutionary strategies in lizard reproduction. Evolution2455-74.

TokarzR.R. (1985) Body size as a factor determining dominance in stage agonistic encounters between male brown anoles (Anolis sagrei). Anim. Behav.33746-753.

VogrinN. (1999) Preliminary note on the morphometric differences between two populations of Podarcis muralis muralis (Laurenti, 1768) and Podarcis muralis maculiventris (Werner, 1891) in Slovenia. Nat. Croat.8325-329.

VollonoC. & GuarinoF.M. (2002) Analisi scheletrocronologica in alcune specie di Anfibi e rettili del Parco Regionale del Matese. In: G. Odierna & F.M. Guarino (Eds) I Vertebrati Ectotermi del Parco Regionale del Matese pp. 163-171. Centro Stampa dell’Universita degli Studi di Napoli Federico IINaples, Italy.

WapstraE.SwanR. & O’ReillyJ.M. (2001) Geographic variation in age and size at maturity in a small Australian viviparous skink. Copeia2001646-655.

WilliamsG.C. (1966) Adaptation and Natural Selection. Princeton University PressPrinceton, NJ, USA.


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    Age distributions for male and female P. muralis from the Dereköy (A) and Kazdağı (B) populations.

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    Von Bertalanffy growth curves for males (open circles, solid line) and females (solid circles, dashed line) of P. muralis from the Dereköy (A) and Kazdağı (B) populations. The open square shows snout-vent length mean of the lizards at hatching as reported by In den Bosch & Bout (1998). Growth parameters are given in the text.

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    Hematoxylin sections (8 μm thick) through phalanges of male (A) and female (B) P. muralis. (A) Five-year-old male (57.8 mm SVL) from the Dereköy population. (B) Eight-year-old female specimen (60.0 mm SVL) from the Kazdağı population. Abbreviations: MC, marrow cavity; EB, endosteal bone; RL, resorption line; P, periphery.

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    Descriptive statistics of age, snout-vent length (SVL) and growth rates for both populations. Abbreviations: CI, confidence intervals; GR, growth rate; k, growth coefficient; n, number of samples; SE, standard error.

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