SciELO - Scientific Electronic Library Online

 
vol.30 número1Primer registro de la sanguijuela Oxyptychus inexpectatus depredando sobre Pleurodema somuncurense y Rhinella arenarum en la meseta de Somuncura, Rio Negro, ArgentinaRhinella major (Anura: Bufonidae) and Leptodactylus macrosternum (Anura: Leptodactylidae): predation and cannibalism by Leptodactylus macrosternum índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Journal

Artigo

Indicadores

  • Não possue artigos citadosCitado por SciELO

Links relacionados

Compartilhar


Cuadernos de herpetología

versão On-line ISSN 1852-5768

Cuad. herpetol. vol.30 no.1 San Salvador de Jujuy maio 2016

 

NOTA

Injured Salvator merianae (Teiidae) regenerates six tails in central Argentina

Nicolás Pelegrin, Suelem Muniz Leão

Instituto de Diversidad y Ecología Animal (CONICET-UNC) and Centro de Zoología Aplicada (UNC). Rondeau 798, X5000AVP Córdoba, Argentina.

Recibida: 02/07/15
Revisada: 08/08/15
Aceptada: 10/09/15


ABSTRACT

Some lizards have the ability of partially regenerate many tissues like nerve cells, part of the mandible, and parts of the limbs; and most of them can regenerate the tail. Tail autotomy followed by tail regeneration is a strategy widely used in lizards to escape from predators. In some cases tail breaks but it does not detaches completely from the body, leading to a regenerated tail with multiple tips. Here we report a young individual of Salvator merianae from central Argentina that presented six regenerated tails growing from a major injury in its tail.

Lizards are able of regenerate many tissues. Some studies reported regeneration of axons (McLean and Vickaryous, 2011; Zika, 1969), partial regeneration of the lower mandibular arch (Werber, 1905) and of limbs (Bellairs and Bryant, 1985), and have a noteworthy ability to regenerate the tail (Alibardi, 2009). Tail autotomy followed by tail regeneration is a strategy widely used in lizards to escape from predators (Vitt and Caldwell, 2009). In response to a predatory stimulus, tails are voluntarily detached by the individual at an specific fracture plane in vertebrae. Tail detachment is facilitated by autotomy septa that pass through the musculature, and mechanisms for rapidly closing off blood vessels. After tail loss, tail stubs heal rapidly and regeneration begins (Bateman and Fleming, 2009; Vitt and Caldwell, 2009). In the process of tail regeneration vertebrae do not regenerate, and they are replaced by a cartilaginous rod (Alibardi, 2009).

Shedding the tail has costs and benefits for lizards. While it is a strategy to avoid predation (but see Downes and Shine, 2001), it may affect several aspects of lizard ecology like reproduction (Dial and Fitzpatrick, 1981; Martin and Salvador, 1993), intraspecific signaling (Fox et al., 1990), habitat use (Martín and Salvador, 1992), and moving patterns (Martin and Avery, 1998).

In some cases the tail breaks but it does not detaches completely from the body, leading to a rege­nerated tail with two or even three tips (a trifurcated tail) (Pheasey et al., 2014). Tail bifurcation has been reported for many lizard families like Gymnophtal­midae (Pheasey et al., 2014), Scincidae (Hickman, 1960), Tropiduridae (Martins et al., 2013; Passos et al., 2014), Lacertidae (Renet, 2013), Agamidae (Ananjeva and Danov, 1991), Teiidae (Gogliath et al., 2012), and Gekkonidae (Ali, 1948).

In this note we report an exceptional case of a young individual (SVL: 301 mm) of Salvator meria­nae Linnaeus, 1758 from central Argentina with six regenerated tails. The specimen was found in the city of Córdoba (31°19'S, 64°15'W) in January 2014. It presented evidence of a severe injury that extended dorsally through the entire length of the tail. Injury appeared to be inflicted with a sharp object that cut off the tissue. Normal scalation pattern was severely altered in the damaged area, and had the aspect of a dry wound, rather than a regenerated tissue due to its darkish coloration. Regenerated tails of different size arise at six different points. Most of the tails arise perpendicularly to the axis of the original tail (Fig. 1). One of the tails (numbered 4 in Fig. 1) bends abruptly after its origin at an angle of 90º. At the end of the tail, two regenerated tails grew from the last vertebrae (Fig. 1). An x-ray image showing origin points of each regenerated tail can be seen in Fig. 2. Autotomy planes within vertebrae can be recognized in the image (Fig. 2).


Figure 1. Specimen of S. merianae presenting six regenerated tails. Note the wound (black area) extending dorsally along the tail.


Figure 2. X-Ray image of the hexafurcated tail. Enlarged area 1 indicates a bifurcated regeneration produced in a single breakage point. Arrows in enlarged area 2 shows autotomy plans within the vertebrae.

Researchers have evaluated the costs of tail loss in lizards (summarized in Bateman and Fleming, 2009), but no studies are available in literature about the costs of abnormal tail regeneration. Extreme cases like the one reported here are extremely rare and probably have higher associated costs. Metabolic costs of multiple tails, and how fat reserves are distributed and allocated in multiple regenerated tails are interesting questions to be answered in future studies.

Acknowledgements

The specimen was brought to Centro de Zoología Aplicada (UNC) by members of División de Patrulla Ambiental of Córdoba Police. We thank Dirección de Fauna of Secretaría de Ambiente de Córdoba for permission to study the specimen. Leão, S.M. has a fellowship from CONICET/Argentina and CNPq/Brazil. Two anomymous reviewers provided useful comments to the manuscript.

 

Literatura citada

1. Ali, S.M. 1948. Studies on the anatomy of the tail in Sauria and Rhynchocephalia. Proceedings of the Indian Academy of Sciences - Section B 28: 151-165.         [ Links ]

2. Alibardi, L. 2009. Morphological and cellular aspects of tail and limb regeneration in lizards: A model system with implications for tissue regeneration in mammals. Vol. 207. Springer-Verlag, Berlin.         [ Links ]

3. Ananjeva, N.B. & Danov, R.A. 1991. A rare case of bifurcated caudal regeneration in the Caucasian agama, Stellio caucasius. Amphibia-Reptilia 12: 343-349.         [ Links ]

4. Bateman, P.W. & Fleming, P.A. 2009. To cut a long tail short: a review of lizard caudal autotomy studies carried out over the last 20 years. Journal of Zoology 277: 1-14.         [ Links ]

5. Bellairs, A.D. & Bryant, S. V. 1985. Autotomy and regeneration in reptiles: 303-410. In: Gans, C. & Billett, F. (eds.), Biology of the Reptilia. Volume 15. Development B. John Wiley & Sons, New York.         [ Links ]

6. Dial, B.E. & Fitzpatrick,L.C. 1981. The energetic costs of tail autotomy to reproduction in the lizard Coleonyx brevis (Sauria: Gekkonidae). Oecologia 51: 310-317.         [ Links ]

7. Downes, S. & Shine, R. 2001. Why does tail loss increase a lizard's later vulnerability to snake predators? Ecology 82: 1293-1303.         [ Links ]

8. Fox, S.F.; Hegerand, N.A. & Delay, L.S. 1990. Social cost of tail loss in Uta stansburiana: lizard tails as status-signalling badges. Animal Behaviour 39: 549-554.         [ Links ]

9. Gogliath, M.; Pereira, L.C.M.; Nicola, P.A. & Ribeiro, L.B. 2012. Ameiva ameiva (Giant Ameiva). Bifurcation. Herpetological Review 43: 129.         [ Links ]

10. Hickman, J. 1960. Observations on the skink lizard Egernia whitii (Lacepede). Papers and Proceedings of the Royal Society of Tasmania. 94: 111-119.         [ Links ]

11. Martin, J. & Avery, R. 1998. Effects of tail loss on the movement patterns of the lizard, Psammodromus algirus. Functional Ecology 12: 794-802.         [ Links ]

12. Martín, J. & Salvador, A. 1992. Tail loss consequences on habitat use by the Iberian rock lizard, Lacerta monticola. Oikos 65: 328-333.         [ Links ]

13. Martin, J. & Salvador, A. 1993. Tail loss reduces mating success in the Iberian rock-lizard, Lacerta monticola. Behavioral Ecology and Sociobiology 32: 185-189.         [ Links ]

14. Martins, R.L.; Peixoto, P.G.; Fonseca, P.H.; Martinelli, A.G.; Silva, W.R. & Pelli, A. 2013. Abnormality in the tail of the collated lizard Tropidurus gr. torquatus (Iguania, Tropiduridae) from Uberaba city, Minas Gerais State, Brazil. Herpetology Notes 6: 369-371.         [ Links ]

15. McLean, K.E. & Vickaryous, M.K. 2011. A novel amniote model of epimorphic regeneration: the Leopard Gecko, Eublepharis macularius. BMC Developmental Biology 11: 50.         [ Links ]

16. Passos, D.C.; Pinheiro, L.T.; Galdino, C.A.B. & Rocha, C.F.D. 2014. Tropidurus semitaeniatus (Calango de Lagedo). Tail bifurcation. Herpetological Review 45: 138.         [ Links ]

17. Pheasey, H.; Smith, P.; J.-P.Brouardand K. Atkinson. 2014. Vanzosaura rubricauda (red-tailed vanzosaur) bifurcation and trifurcation. Herpetological Review 45: 138-139.         [ Links ]

18. Renet, J. 2013. Deux cas d'anomalie caudale chez le Lézard ocellé Timon lepidus lepidus (Daudin, 1802) dans le sud-est de la France (Bouches-du-Rhône). Nature de Provence - Revue du CEN PACA 2: 99-101.         [ Links ]

19. Vitt, L.J. & Caldwell, J.P. 2009. Herpetology. An Introductory Biology of Amphibians and Reptiles. 3rd ed. Academic Press, Burlington.         [ Links ]

20. Werber, I. 1905. Regeneration der Kiefer bei der Eidechse Lacerta agilis. Wilhelm Roux. Archiv für Entwicklungsmechanik der Organismen 19: 248-258.         [ Links ]

Creative Commons License Todo o conteúdo deste periódico, exceto onde está identificado, está licenciado sob uma Licença Creative Commons