Dergiler / Communications Faculty of Sciences University of Ankara Series C Biology / 2026 / Volume: 32 Issue: 1

Sexual dimorphism in the lacertid lizard Apathya cappadocica (Werner, 1902) (Reptilia: Lacertidae) from southeastern Türkiye

Kamil Candan(DOKUZ EYLÜL ÜNİVERSİTESİ)0000-0002-6934-3971
Elif Yıldırım(DOKUZ EYLÜL ÜNİVERSİTESİ)0000-0001-9614-5754
Yusuf Kumlutaş(DOKUZ EYLÜL ÜNİVERSİTESİ)0000-0003-1154-6757
Osman Sinan Günister(DOKUZ EYLÜL ÜNİVERSİTESİ)0000-0002-4483-8097
Çetin Ilgaz(DOKUZ EYLÜL ÜNİVERSİTESİ)0000-0001-7862-9106
Sayfa
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Yayın Tarihi
2023-06-03
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

In conclusion, it can be accepted that the species in the genus Apathya has a similar pattern in accordance with the larger male theory.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Apathya cappadocica is a medium-sized lizard species included in the family Lacertidae.
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Temel Bulgular & Veri:A total of 87 adult lizard specimens collected from south-eastern Anatolia were used in this study.
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Sonuç & Katkı:In conclusion, it can be accepted that the species in the genus Apathya has a similar pattern in accordance with the larger male theory.
🔬Tür:Research Article
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Apathya cappadocica · lizard · sexual dimorphism

Abstract

Apathya cappadocica is a medium-sized lizard species included in the family Lacertidae. The species is known from Türkiye, Northern Syria, Iraq, and Western Iran. Sexual dimorphism (SD), which is a phenomenon including phenotypic differences between males and females, has many effects on behaviour, shape and size characteristics. A total of 87 adult lizard specimens collected from south-eastern Anatolia were used in this study. The results of ANOVA showed that all morphometric features exhibited a pattern in which males have larger size than females. According to principal component analysis (PCA), the first three factors explain 81.553% of the total variance. Differences in head size between sexes have been well-documented in lizards and are associated with male-male aggression which results in mating success. This kind of pattern is supported by this study. Additionally, the results showed that males have more femoral pores, which is a signalling mechanism for sexual selection, than females. In conclusion, it can be accepted that the species in the genus Apathya has a similar pattern in accordance with the larger male theory.

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Bu Makaleye Atıf Yap

Candan, K., Yıldırım, E., Kumlutaş, Y., Günister, O. S., Ilgaz, Ç. (2023). Sexual dimorphism in the lacertid lizard Apathya cappadocica (Werner, 1902) (Reptilia: Lacertidae) from southeastern Türkiye. Communications Faculty of Sciences University of Ankara Series C Biology, Volume: 32 Issue: 1. https://doi.org/10.53447/communc.1185771

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Kaynakça (38)

  1. Arnold, E.N., Arribas, O., Carranza, S., Systematics of the Palaearctic and Oriental lizard tribe Lacertini (Squamata: Lacertidae: Lacertinae), with descriptions of eight new genera. Zootaxa, 1430 (2007), 1–86. https://doi.org/10.11646/zootaxa.1430.1.1
  2. Kapli, P., Botoni, D., Ilgaz, Ç., Kumlutaş, Y., Avcı, A., Rastegar-Pouyani, N., Poulakakis, N., Molecular phylogeny and historical biogeography of the Anatolian lizard Apathya (Squamata, Lacertidae). Mol. Phylogenet. Evol., 66 (2013), 992–1001. https://doi.org/10.1016/j.ympev.2012.12.002
  3. Baran, İ., Avcı, A., Kumlutaş, Y., Olgun, K. Ilgaz Ç., Türkiye Amfibi ve Sürüngenleri, Palme Yayınevi, 2021.
  4. Gül, S., Özdemir, N., Avcı, A., Kumlutaş, Y., Ilgaz, Ç., Altitudinal effects on the life history of the Anatolian lizard (Apathya cappadocica, Werner 1902) from southeastern Anatolia, Turkey. Turkish Journal of Zoology, 39 (2015), 507-512. https://doi.org/ 10.3906/zoo-1407-6
  5. Karamiani, R., Dabid, S., Rastegar-Pouyani, N., Sexual dimorphism of the Yassujian Lizard, Apathya yassujica (Nilson et al, 2003) (Sauria: Lacertidae) from Iran. Amphibian and Reptile Conservation, 9 (2015), 42–48.
  6. Hosseinian Yousefkhani, S.S., Rastegar-Pouyani, E., Ilgaz, Ç., Kumlutaş, Y., Avcı, A., Wink, M., Evidences for ecological niche differentiation on the Anatolian lizard (Apathya cappadocica ssp.) (Reptilia: Lacertidae) in western Asia. Biologia, 74 (2019), 1661–1667. https://doi.org/10.2478/s11756-019-00273-4
  7. Carothers, J.H., Sexual selection and sexual dimorphism in some herbivorous lizards. The American Naturalist, 124 (1984), 244–254.
  8. Andersson, M., Sexual selection, Princeton: Princeton University Press, 1994.
  9. Olsson, M., Shine, R., Wapstra, E., Ujvari, B., Madsen, T., Sexual dimorphism in lizard body shape: the roles of sexual selection and fecundity selection. Evolution, 56 (2002), 1538-1542. https://doi.org/10.1111/j.0014-3820.2002.tb01464.x
  10. Thompson, G., Withers, P., Size-free shape differences between male and female western Australian dragon lizards (Agamidae), Amphibia-Reptilia, 26 (2005), 55-63. https://doi.org/10.1163/1568538053693332
  11. Adriana, C.S., Helga, C.W., Guarino, R.C., Sexual dimorphism in the Neotropical lizard, Tropidurus torquatus (Squamata, Tropiduridae). Amphibia-Reptilia, 26 (2005), 127-137. https://doi.org/10.1163/1568538054253384
  12. Cooper, W.E., Greenberg, J.N., Reptilian coloration and behavior. In: Gans, C., Crews, D. editor. Biology of the Reptilia: Hormones, Brain, and Behavior. University of Chicago Press, Chicago, IL, USA, (1992), 298-422.
  13. Herrel, A., Spithoven, L., Van Damme, R., De Vree, F., Sexual dimorphism of head size in Gallotia galloti: testing the niche divergence hypothesis by functional analyses. Functional Ecology, 13 (1999), 289-297. https://doi.org/10.1046/j.1365-2435.1999.00305.x
  14. Cox, R.M., Skelly, S.L., John-Alder, H.B., A comparative test of adaptive hypotheses for sexual size dimorphism in lizards. Evolution, 57 (2003), 1653-1669. https://doi.org/10.1111/j.0014-3820.2003.tb00371.x
  15. Heidari, N., Faizi, H., Rastegar-Pouyani, N., Sexual dimorphism in Blanford’s Fringe-toed Lizard, Acanthodactylus blanfordi Boulenger, 1918, from Southern Iran: (Sauria: Lacertidae). Zoology in the Middle East, 55 (2012), 35–40. https://doi.org/10.1080/09397140.2012.10648915
  16. Oraie, H., Rahimian, H., Rastegar-Pouyani, N., Khosravani, A., Rastegar-Pouyani, E., Sexual size dimorphism in Ophisops elegans (Squamata: Lacertidae) in Iran. Zoology in the Middle East, 59 (2013), 302–307. https://doi.org/10.1080/09397140.2013.868131
  17. Fitch, H.S., Sexual size differences in reptiles. Misc. Pub. Mus. Nat. Hist., 70 (1981), 1–72.
  18. Stamps, J., Sexual selection, sexual dimorphism and territoriality. In: Huey, R.B., Pianka E.R., Schoener T.W. editors. Lizard Ecology: Studies of a Model Organism. Cambridge: Harvard University Press., (1983), 169–204.
  19. Cox, R.M., Butler, M.A., John-Alder, H.B., The evolution of sexual size dimorphism in reptiles. In: Fairbairn, D.J,, Blanckenhorn, W,U, Szekely, T., editors. Sex, Size & Gender Roles: Evolutionary Studies of Sexual Size Dimorphism. Oxford University Press, (2007), 38–49.
  20. Eiselt, J., Ergebnisse zoologischer sammelreisen in der Türkei Lacerta cappadocica Werner, 1902 (Lacertidae, Reptilia). Ann. Naturhist. Mus. Wien, 82 (1979), 387–421.
  21. Nilson, G., Rastegar-Pouyani, N., Rastegar-Pouyani, E., Andrén, C., Lacertas of south and central Zagros Mountains, Iran, with description of two new taxa. Russ. J. Herpetol., 10 (2003), 11-24. https://doi.org/10.30906/1026-2296-2003-10-1-11-24
  22. Fairbairn, D.J., Blanckenhorn, W.U., Székely, T., Sex, Size, and Gender Roles Evolutionary Studies of Sexual Size Dimorphism. Oxford University Press, New York, 2007.
  23. Dehghani, A., Hosseinian Yousefkhani, S.S., Rastegar-Pouyani, N., Banan-Khojasteh, S.M., Mohammadpour, A., Sexual size dimorphism in Darevskia raddei (Sauria: Lacertidae) from northwestern Iran. Zoology in the Middle East, 60 (2014), 120–124. https://doi.org/10.1080/09397140.2014.914715
  24. Rensch, B., Die Abhangigkeit der relativen sexualdifferenz von der Korpergrole. Bonner Zoologische Beitrage, 1 (1950), 58-69.
  25. Abouheif, E., Fairbairn, D.J., A comparative analysis of allometry for sexual size dimorphism: Colwell, R. K. 2000. Rensch’s rule crosses the line: convergent allometry of sexual size dimorphism in hummingbirds and flower mites. The American Naturalist, 156 (1997), 495-510.
  26. Colwell, R.K., Rensch’s rule crosses the line: convergent allometry of sexual size dimorphism in hummingbirds and flower mites. Am. Nat., 156 (2000), 495–510.
  27. Karamiani, R., Rastegar-Pouyani, N., Fattahi, R., Fathinia, B., Sexual dimorphism in leaf-toed gecko Asaccus elisae (Werner, 1895) (Sauria: Gekkonidae) from western Iran. Hamadryad, 36 (2013), 157–161.
  28. Şahin, M.K., Kumlutaş, Y., Ilgaz, Ç., Sexual dimorphism in spiny - tailed lizard, Darevskia rudis (Bedriaga, 1886) (Sauria: Lacertidae), from Northeastern Anatolia, Turkey. AKU J. Sci. Eng., 20 (2020), 551-557. https://doi.org/10.35414/akufemubid.714889
  29. Olsson, M., Contest success in relation to size and residency in male sand lizards, Lacerta agilis. Animal behaviour, 44 (1992), 386–388. https://doi.org/10.1016/0003-3472(92)90046-C
  30. Huang, W.S., Sexual size dimorphism and microhabitat use of two sympartric lizards, Sphenomorphus taiwanensis and Takydromus hsuehshanensis, from the Central Highlands of Taiwan. Zoological Studies-Taipei, 37 (1998), 302–308.
  31. Ji, X., Zhou, W.H., Zhang, X.D., Gu, H.Q., Sexual dimorphism and reproduction in the grass lizard Takydromus septentrionalis. Russian Journal of Herpetology, 5 (1998), 44‐48. https://doi.org/10.30906/1026-2296-1998-5-1-44-48
  32. Molina-Borja, M., Padron‐Fumero, M., Alfonso‐Martin, T., Morphological and behavioural traits affecting the intensity and outcome of male contestes in Gallotia galloti galloti (family Lacertidae). Ethology, 104 (1998), 314‐322. https://doi.org/10.1111/j.1439-0310.1998.tb00071.x
  33. Chang, M.H., Oh, H.S., Sexual size dimorphism of lacertid lizards from Korea. Korean Journal of Environment and Ecology, 26 (2012), 668–674.
  34. Lappin, A.K., Husak, J.F., Weapon performance, not size, determines mating success and potential reproductive output in the collared lizard (Crotaphytus collaris). The American Naturalist, 166 (2005), 426–436. https://www.journals.uchicago.edu/doi/10.1086/432564
  35. Kratochvíl, L., Frynta, D., Body-size effect on egg size in eublepharid geckos (Squamata: Eublepharidae), lizards with invariant clutch size: negative allometry for egg size in ectotherms is not universal. Biological Journal of the Linnean Society, 88 (2002), 527-532. https://doi.org/10.1111/j.1095-8312.2006.00627.x
  36. Martín, J., López, P., Interpopulational differences in chemical composition and chemosensory recognition of femoral gland secretions of male lizards Podarcis hispanica: implications for sexual isolation in a species complex. Chemoecology, 16 (2006), 31–38. https://doi.org/10.1007/s00049-005-0326-4
  37. Gabirot, M., Lopez, P., Martin, J., De Fraipont, M., Heulin, B., Sinervo, B., Clobert, J., Chemical composition of femoral secretions of oviparous and viviparous types of male common lizards Lacerta vivipara. Biochemical Systematics and Ecology, 36 (2008), 539–544. https://doi.org/10.1016/j.bse.2008.03.006
  38. Iraeta, P., Monasterio, C., Salvador, A., Diaz, J.A., Sexual dimorphism and interpopulation differences in lizard hind limb length: locomotor performance or chemical signalling?. Biological Journal of the Linnean Society, 104 (2011), 318–329. https://doi.org/10.1111/j.1095-8312.2011.01739.x