ISSN 1827-9635 (print) © Firenze University Press ISSN 1827-9643 (online) www.fupress.com/ah Acta Herpetologica 7(2): 309-313, 2012 Evidence of high longevity in an Island lacertid, Teira dugesii (Milne-Edwards, 1829). First data on wild specimens J. Jesus Centro de Competências de Ciências da Vida, Universidade da Madeira, Campus Universitário da Penteada, 9020-105 Funchal, Portugal. E-mail: jesus@uma.pt Submitted on: 2012, 13th March; revised on: 2012, 23rd April; accepted on: 2012, 18th April. Abstract. Using the technique of capture, mark and recapture, here is reported a case of high longevity in the Madeiran lizard, Teira dugesii. It is one of the highest reported values for lacertid lizards (16 years or more) in a wild population. Keywords. Longevity, Teira dugesii, Madeira island. Teira dugesii is a lacertid lizard endemic to the Madeiran Archipelago, and was intro- duced to some islands of the Azores in the XIX century (Malkmus, 1985, 2004) and to the harbour area of Lisbon (Sá Sousa, 1995). It is an omnivorous and oportunistic lacer- tid that inhabits a wide range of habitats, from sea level to the highest altitude of Madei- ra Archipelago (1871 m – Pico Ruivo, Madeira Island). It can be found in almost every island/islet of the archipelago (Jesus et al., 2009). Since the earliest 1990’s we have being studying T. dugesii in their native environ- ments. Most of the studies dealt with phylogeny and population genetics (e.g. Brehm et al. 2001, 2002, 2003; Jesus et al., 2005a). Other studies have also been performed in this species, for example on diet (Sadek, 1981), predation (Jesus et al., 2005b), morphological variability (Cook, 1979; Báez and Brown, 1997; Jesus et al., 2006), and colour pattern vari- ability (Crisp et al., 1979; Báez, 1990). Curiously, no data exists on longevity in wild popu- lations in the native area. The ecological aspects and life histories traits of wild popula- tions are practically unknown, with a few studies performed on captive lizards (e.g., Galan and Vicente, 2003). In 1996 we started capture-mark recapture sessions on Madeiran lizards to study growth, and some other aspects such as time of courtship, pregnancy, egg laying, hatch- ling and male maturation cycles, using toe-clipping. Sessions lasted two years and several captures/recaptures were performed essentially in four localities of Madeira Island, using pitfall traps. The first was Ponta de São Lourenço located in the Eastern part of the Island, at approximately 70 m of altitude, a notably arid location. The second locality was Pico 310 J. Jesus do Arieiro, with 1850 m of altitude, in the central mountain ridge, the third was Curral das Freiras, with 950m of altitude, in a inland position in the island, and the fourth was Ribeira do Alecrim, Paul da Serra, a plateau in the western part of the Island, in the Cen- tral Mountain Ridge at about 1300 m. In 2006, a unique event occurred in Paul da Serra. Two (individuals 105 and 108) of the 7 lizards that were caught, were recaptured. According to SVL values, in 1997, the individuals 105 and 108 were probably around or less than one year old (Table 1). For- ty-six mm is the typical size of juveniles. Although variation exists, according to Cook (1979), animals of 45 mm or less are probably less than one year old. Juveniles and young adults between 46 and around 60 are one or two years old, while larger ones are older mature adults. In 2011, another session of capture was performed. Eighteen lizards were captured, three of which were recaptures. Individual 10 was probably one year old in July 1996. Regarding individual 204, it was difficult to estimate the age although probably, in Sep- tember 2006, it was at least 2 years old (Table 2). The most unexpected value belongs to individual 500. In 1997 it was already an adult female. The SVL at that time suggests that the female was older than 2 years, and probably was born in 1995 or earlier, making her at least 16 years old in 2011. In this population males with SVL longer than 75 (and even 80) mm are frequent, and it is even possible to find females with a similar size, almost reaching a SVL of 80 mm. Thus, although variability exists, there is a high probability to find females that are even older than this one. Table 1. Date of captures and SVL of individuals 105 and 108 from Paúl da Serra Individual 105 (Female) Individual 108 (Male) Date SVL (mm) Date SVL (mm) 02 Jun 1997 59 23 Jun 1997 46 15 Apr 1999 65 06 Sep 2006 66 06 Sep 2006 70 In 2006: 9 years * In 2006: 9 years* * Estimated age Table 2. Date of captures and SVL of individuals 105 and 108 of Paúl da Serra Individual 10 (Female) Individual 204 (Male) Individual 500 (Female) Date SVL Date SVL Date SVL 10 Jul 1996 54 02 May 1997 67 15 Apr 1999 66 06 Sep 2006 68 19 Jul 2011 73 19 Jul 2011 78 19 Jul 2011 75 At least 15 years * At least 6 years* At least 16 years* * Estimated age 311High longevity in Teira dugesii In 2011, one session of capture was performed in Pico do Arieiro, another high-alti- tude site, separated from Paul da Serra by deep valleys. Nine individuals were captured, of which one (individual 75) was a recapture (Table 3). Probably in 1997, this individual was at least two years old, and was born in 1995 or earlier. In 2011, two attempts of capture in Ponta de São Lourenço were performed. Fifty- seven lizards were captured and none were marked. These longevities are high when compared with other lacertid species, although most of the published data are from terrarium animals. Slavens and Slavens (1992, 1993) reported high longevities for captive reptiles including lacertids. For example they refer the following maximum ages: Timon lepidus, 14 years and 5 months; Lacerta trilineata, one individual 7 years and 9 months old and another 4 years and 4 months old; Gallo- tia galloti, 5 years; Podarcis pityusensis, 4 years and 7 months (still living at that time). A specimen of T. lepidus living in Museum Koenig has an estimated age of at least 28 years (Philipp Wagner, pers comm). Bannert (1998) refers higher values for captive lac- ertid lizards, with 12 years for Gallotia atlantica, Gallotia caesaris and T. dugesii, 13 years for Gallotia stehlini, Lacerta bilineata and Podarcis hispanica, 15 years for Gallotia galloti eisentrauti and Podarcis tiliguerta and 18 years for P. pityusensis. The value for T. dugesii is lower than our estimated age for wild specimens of this species. According to Avery (1975) the mean expectation of life for Zootoca vivipara was about 5 years. Saint Girons et al. (1989) obtained different longevities in two populations of Lacerta viridis (5 and 8 or more). For Podarcis muralis, Castanet and Roche (1981) obtained 6 years, Bourliére (1946) 4 to 6 years, and Flower (1937) 4 to 10 years. In Lacerta agilis, in an Alpine area of Italy Guarino et al. (2010) found that longevity was 4 years for males and 3 for females. In the same species, living in Daghestan (Russia), Roitberg and Smirina (2006) found longevities of 6 years for males and 5 years for females in the popu- lation from lowland and submontane regions (until 600 m. a.s.l.), but 7 years for males and 6 years for females in the population from highlands (starting from 960 m. a.s.l), emphasizing the variability in longevity. In the western coast of Sweden Olsson and Shine (1996) also observed in L. agilis that maximum longevity was 11 years for males and 12 for females. Although high, this value is still lower than that observed for T. dugesii. Although the data is limited, an interesting aspect is that the longevity seems to be high- er in high altitude populations. However, further captures are needed at different altitudes to confirm this. Normally, these high longevities are common on islands forms, such as Gallo- tia simonyi (20 years) (Castanet and Báez, 1991) and the extinct scincid Macroscincus coctei Table 3. Date of captures and SVL of individuals 105 and 108 of Paúl da Serra Individual 75 (Male) Date SVL (mm) 06 Mar 1997 69 07 Aug 2011 74 At least 15 years * * Estimated age 312 J. Jesus (16 years) (Andreone and Guarino, 2003). T. dugesii is usually much smaller than these two species, so it is probably one of the smallest lacertid lizard with such a high longevity. Finally, this finding could be in accordance to the island theory, which states that spe- cies tend to have higher longevity than their mainland relatives (Blondel, 1986). In fact, despite the lack of published data, there is evidence that Scelarcis perspicillata, regarded as the mainland sister taxon to T. dugesii (Harris et al., 1998), has lower longevity, about 4-5 years (Ana Perera, pers comm). ACKNOWLEDGEMENTS I would like to acknowledge my friend James Harris for helpful suggestions and assistance. I am also grateful to Philipp Wagner and Dan Cogalniceanu and Sergé Bogaerts for the precious bib- liography and comments on reptile longevity. REFERENCES Andreone, F., Guarino, F. (2003): Giant and long-lived? Age structure in Macroscincus coctei, an extinct skink from Cape Verde. Amphibia-Reptilia 24: 459-470. Avery, R. (1975): Age-structure and longevity of Common lizard (Lacerta vivipara) popu- lations. J. Zool. 176: 555-558. Báez, M. (1990): Observaciones sobre colorido y diseño de Podarcis dugesii en la isla de Madeira. Vieraea 18: 197-203. Báez, M., Brown, R. (1997): Testing multivariate patterns within-island differentiation in Podarcis dugesii from Madeira. J. Evol. Biol. 10: 575-587. Bannert, B. (1998): Zur Lebenserwartung Lacertiden im Terrarium. Die Eidechse 9: 59-66. Blondel, J. (1986): Biogéographie Évolutive. Masson, Paris. Bourliére, F. (1946): Longevité moyene et logevité maximum chez les Vertébrés. Année boil. 22: 249-270. Brehm, A., Khadem, M., Jesus, J., Andrade, P., Vicente, L. (2001): Lack of congruence between morphometric evolution and genetic differentiation suggests a recent dis- persal and loal habitate adaptation of the madeiran lizard Lacerta dugesii. Genet. Sel. Evol. 33: 671-685. Brehm, A., Harris, D.J., Alves, C., Jesus, J., Thomarat, F., Vicente, L. (2002): Structure and evolution of the mitochondrial DNA complete control region in the lizard Lacerta dugesii (Lacertidae, Sauria). J. Mol. Evol. 55: 1-8. Brehm, A., Jesus, J., Spínola, H., Alves, C., Vicente, L., Harris, D. J. (2003): Phylogeogra- phy of the madeiran endemic lizard Lacerta dugesii inferred from mtDNA sequenc- es. Mol. Phylogenet. Evol. 26: 222-230. Castanet, J., Báez, M. (1991): Adaptation and evolution in Gallotia lizards from the Canary Islands: age, growth, maturity and longevity. Amphibia-Reptilia 12: 81-102. Castanet, J., Roche, E. (1981): Détermination de l’âge chez le lézard des murailles, Lacerta muralis (Laurenti, 1768) au moyen de la squelletochronologie. Rev. Suisse Zool. 88: 215-226. 313High longevity in Teira dugesii Cook, L. (1979): Variation in the Madeiran Lizard Lacerta dugesii. J. Zool. 187: 327-340. Crisp, M., Cook, L., Hereward, F. (1979): Color and heat balance in the lizard Lacerta dug- esii. Copeia 1979: 250-258. Flower, S. (1937): Further notes on the duration of life in animals. III- Reptiles. Proc. Zool. Soc. Lond. 107:1-39. Galán, P., Vicente, L. (2003). Reproductive characteristics of the insular lacertid Teira dug- esii. Herpetol. J. 13: 149-153. Guarino, F., Già, I., Sindaco, R. (2010): Age and growth of the sand lizards (Lacerta agilis) from a high Alpine population of north-western Italy. Acta Herpetol. 5: 23-29. Harris, D.J., Arnold, E.N., Thomas, R.H. (1998): Relationships of lacertid lizards (Reptilia: Lacertidae) estimated from mitochondrial DNA sequences and morphology. Proc. R. Soc. Lond. B 265: 1939–1948. Jesus, J., Brehm, A., Harris, D.J. (2005a): Is c-mos phylogenetically informative at lower taxonomic levels in reptiles ? An assessment of variation within Lacerta (Teira) dug- esii Milne-Edwards, 1829 (Squamata: Sauria: Lacertidae). Herpetozoa 18: 55-59. Jesus, J., Sampaio, L., Silva, L. (2005b): Incidence of Lacerta dugesii Milne-Edwards, 1829 (Sauria, Lacertidae) in the diet of kestrels (Falco tinnunculus canarinsis Koenig, 1889; Aves, Falconidae) in a semiarid zone of Madeira. Herpetol. Bull. 93: 14-16. Jesus, J., Sampaio, L., Crespo, E. (2006): High frequency of lack of occipital scale in madeiran lizard Lacerta dugesii Milne-Edwards, 1829 (Sauria, Lacertidae), on a very small island, Selvagem Pequena (Selvagens, Portugal). Bol. Asoc. Herpetol. Esp. 17: 88-93 Jesus, J., Teixeira, S., Teixeira, D., Freitas, T., Russo, D. (2009): Vertebrados terrestres autóctones dos Arquipélagos da Madeira e Selvagens. Direcção Regional de Ambi- ente. Funchal. Malkmus, R. (1985): Zur verbreitung von Rana perezi und Lacerta dugesii auf den Azoren. Nachrichten naturw. Mus. Aschaffenburg 92: 37-69. Malkmus, R. (2004): Amphibians and reptiles of Portugal, Madeira and the Azores-archi- pelago. A.R.G. Gantner Verlag K.G., Ruggell, Germany. Olsson, M., Shine, R. (1996): Does reproductive success increase with age or with size in species with indeterminate growth? A case study using sand lizards (Lacerta agilis). Oecologia 105: 175-178. Roitberg, E., Smirina, E. (2006): 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. 16: 133-148. Sá Sousa, P. (1995): The introduced Madeiran lizard, Lacerta (Teira) dugesii. Amphibia- Reptilia 16: 211-214. Sadek, R. (1981): The diet of the lizard Lacerta dugesii. Biol. J. Linn. Soc. 73: 313-341. Saint Girons, H., Castanet, J., Bradshaw, S., Baron, J. (1989). Démographie comparée de deux populations françaises de Lacerta viridis (Laurenti, 1768). Rev. Ecol. (Terre Vie) 44: 361-386. Slavens, F., Slavens, K. (1992): Reptiles and amphibians in captivity. Breeding-longevity and inventory. Slaveware, Seattle, Washington. Slavens, F., Slavens, K. (1993). Reptiles and amphibians in captivity. Breeding-longevity and inventory. Slaveware, Seattle, Washington. Acta Herpetologica Vol. 7, n. 2 - December 2012 Firenze University Press Advertisement call of species of the genus Frostius Cannatella 1986 (Anura: Bufonidae) Flora A. Juncá1, David L. Röhr2, Ricardo Lourenço-de-Moraes3, Flávio J. M. Santos1, Airan S. Protázio1, Ednei A. Mercês1, Mirco Solé4 Amphibians in Southern Apennine: distribution, ecology and conservation notes in the “Appennino Lucano, Val d’Agri e Lagonegrese” National Park (Southern Italy). Antonio Romano1,*, Remo Bartolomei1, Antonio Luca Conte1, Egidio Fulco2 The significance of using satellite imagery data only in Ecological Niche Modelling of Iberian herps Neftalí Sillero1, José C. Brito2, Santiago Martín-Alfageme3, Eduardo García-Meléndez4, A.G. Toxopeus5, Andrew Skidmore5 Reproductive strategy of male and female eastern spiny lizards Sceloporus spinosus (Squamata: Phrynosomatidae) from a region of the Chihuahuan Desert, México Aurelio Ramírez-Bautista1,*, Barry P. Stephenson2, Xóchitl Hernández-Ibarra1, Uriel Hernández-Salinas1, Raciel Cruz-Elizalde1, Abraham Lozano1, and Geoffrey R. Smith3 Morphological variability of the Hermann’s tortoise (Testudo hermanni) in the Central Balkans Katarina Ljubisavljević1, Georg Džukić1, Tanja D. Vukov1, Miloš L. Kalezić1,2 The usefulness of mesocosms for ecotoxicity testing with lacertid lizards Maria José Amaral1,2,*, Rita C. Bicho1, Miguel A. Carretero2, Juan C. Sanchez-Hernandez3, Augusto M. R. Faustino4, Amadeu M. V. M. Soares1, Reinier M. Mann1,5 Does acclimation at higher temperatures affect the locomotor performance of one of the southernmost reptiles in the world? Jimena B. Fernández*, Nora R. Ibargüengoytía Advertisement call of Scinax littoralis and S. angrensis (Amphibia: Anura: Hylidae), with notes on the reproductive activity of S. littoralis Michel V. Garey1, Thais R. N. Costa2, André M. X. de Lima2, Luís F. Toledo3, Marília T. Hartmann4 Book Review: Marine S. Arakelyan, Felix D. Danielyan, Claudia Corti, Roberto Sindaco, Alan E. Leviton 2011. Herpetofauna of Armenia and Nagorno-Karabakh. Society for the Study of Amphibians and Reptiles Stefano Scali Book Review: Rafaqat Masroor 2012. A contribution to the herpetofauna of Northern Pakistan Stefano Scali Evidence of high longevity in an Island lacertid, Teira dugesii (Milne-Edwards, 1829). First data on wild specimens. J. Jesus First assessment of the endoparasitic nematode fauna of four psammophilous species of Tropiduridae (Squamata: Iguania) endemic to north-eastern Brazil Markus Lambertz1,*, Tiana Kohlsdorf2, Steven F. Perry1, Robson Waldemar Ávila3, Reinaldo José da Silva4 Rediscovery and redescription of the holotype of Lygosoma vittigerum (= Lipinia vittigera) Boulenger, 1894 Yannick Bucklitsch1, Peter Geissler1, Timo Hartmann1, Giuliano Doria2 , André Koch1,* Reproductive phenology of the tomato frog, Dyscophus antongili, in an urban pond of Madagascar’s east coast Ori Segev1,*, Franco Andreone2, Roberta Pala2, Giulia Tessa2, Miguel Vences1 Range extension of the critically endangered true poison-dart frog, Phyllobates terribilis (Anura: Dendrobatidae), in western Colombia Roberto Márquez1,*, Germán Corredor2, Carlos Galvis3 Daniel Góez2, & Adolfo Amézquita1 Differences in habitat use of two sympatric species of Ameiva in East Costa Rica Esther Sebastián-González1, Ramón Gómez2 ACTA HERPETOLOGICA Journal of the Societas Herpetologica Italica