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Helminths infecting the parthenogenetic whiptail lizard Cnemidophorus nativo in a restinga habitat of Bahia State, Brazil

Published online by Cambridge University Press:  12 April 2024

V.A. Menezes
Affiliation:
Departamento de Ecologia, Instituto de Biologia, Universidade do Estado do Rio de Janeiro, 20550-019, Rio de Janeiro, RJ, Brazil
D. Vrcibradic
Affiliation:
Departamento de Ecologia, Instituto de Biologia, Universidade do Estado do Rio de Janeiro, 20550-019, Rio de Janeiro, RJ, Brazil
J.J. Vicente
Affiliation:
Departamento de Helmintologia, Instituto Oswaldo Cruz, 21045-900, Rio de Janeiro, RJ, Brazil
G.F. Dutra
Affiliation:
Departamento de Ecologia, Instituto de Biologia, Universidade do Estado do Rio de Janeiro, 20550-019, Rio de Janeiro, RJ, Brazil
C.F.D. Rocha*
Affiliation:
Departamento de Ecologia, Instituto de Biologia, Universidade do Estado do Rio de Janeiro, 20550-019, Rio de Janeiro, RJ, Brazil
*
*Author for correspondence Fax: 55 21 587 7655 E-mail: cfdrocha@uerj.br

Abstract

A sample of 101 specimens of the unisexual whiptail lizard Cnemidophorus nativo (Squamata; Teiidae) from a coastal site in Bahia State, Brazil were examined for the presence of endoparasites. Of these, 35 (34.7%) harboured helminths. Six helminth species were recovered from C. nativo, including five nematodes (Physaloptera retusa, Physalopteroides venancioi, Subulura lacertilia, Skrjabinelazia intermedia and Parapharyngodon sp., and one cestode (Oochoristica ameivae), all representing new host records. Most lizards were infected by a single species of helminth and none by more than three. Infection rates were neither significantly influenced by host body size nor by environmental factors. The results are compared with data from studies on other whiptail species in both South and North America.

Type
Review Article
Copyright
Copyright © Cambridge University Press 2004

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References

Aho, J.M. (1990) Helminth communities of amphibians and reptiles: comparative approaches to understanding patterns and processes. pp. 157195 in Esch, G.W., Bush, A.O. & Aho, J.M. (Eds) Parasite communities: patterns and processes. New York, Chapman & Hall.CrossRefGoogle Scholar
Alho, C.J.R. (1970) Frequency of infestation by Strongyluris freitasi Alho, 1969 in Tropidurus torquatus (Wied). Revista Brasileira de Biologia 30, 539542.Google Scholar
Ávila-Pires, T.C. (1995) Lizards of Brazilian Amazonia (Reptilia: Squamata). Zoologische Verhandelingen 299, 1706.Google Scholar
Bush, A.O., Aho, J.M. & Kennedy, C.R. (1990) Ecological versus phylogenetic determinants of helminth parasite community richness. Evolutionary Ecology 4, 120.CrossRefGoogle Scholar
Bush, A.O., Lafferty, K.D., Lotz, J.M. & Shostak, A.W. (1997) Parasitology meets ecology in its own terms: Margolis et al. revisited. Journal of Parasitology 83, 575583.CrossRefGoogle Scholar
Caballero, E. & Vogelsang, E.G. (1947) Fauna helmintologica venezolana. I. Ochetosoma miladerocai, n. sp. de Bothrops atrox, L. y hallazgo de Physaloptera retusa Rud., 1819, en Cnemidophorus lemniscatus lemniscatus . Revista de Medicina Veterinaria y Parasitologia 6, 5362.Google Scholar
Chabaud, A.G., Bain, O. & Poinar, G.O. Jr (1988) Skrjabinelazia galliardi (Nematoda, Seuratoidea); complements morphologiques et cycle biologique. Annales de Parasitologie Humaine et Comparée 63, 278284.CrossRefGoogle Scholar
Clayton, D.H. & Moore, J. (1997) Host-parasite evolution: general principles and avian models. 400 pp. Oxford, Oxford University Press.CrossRefGoogle Scholar
Colli, G.R., Caldwell, J.P., Costa, G.C., Gainsbury, A.M., Garda, A.A., Mesquita, D.O., Filho, C.M.M., Soares, A.H.B., Silva, V.N., Valdujo, P.H., Vieira, G.H.C., Vitt, L.J., Werneck, F.P., Wiederhecker, H.C. & Zatz, M.G. (2003a) A new species of Cnemidophorus (Squamata, Teiidae) from the Cerrado biome in central Brazil. Occasional Papers of the Oklahoma Museum of Natural History 14, 114.Google Scholar
Colli, G.R., Costa, G.C., Garda, A.A., Kopp, K.A., Mesquita, D.O., Peres, A.K., Valdujo, P.H., Vieira, G.H.C. & Wiederhecker, H.C. (2003b) A critically endangered new species of Cnemidophorus (Squamata, Teiidae) from a Cerrado enclave in southwestern Amazonia, Brazil. Herpetologica 59, 7688.CrossRefGoogle Scholar
Dias, E.J.R., Rocha, C.F.D. & Vrcibradic, D. (2002) New Cnemidophorus (Squamata: Teiidae) from Bahia State, Northern Brazil. Copeia 2002, 10701077.CrossRefGoogle Scholar
Dutra, G.F. (2000) Tamanho corporal e dieta de Tropidurus torquatus (Sauria: Tropiduridae) em três ilhas do Arquipé-lago dos Abrólhos e em três restingas no extremo sul da Bahia. Unpublished MSc dissertation, Universidade Estadual de Campinas, 80pp.Google Scholar
Dyer, W.G. (1971) Some helminths of the six-lined lizard, Cnemidophorus sexlineatus in South Dakota. Proceedings of the Helminthological Society of Washington 38 256.Google Scholar
Esch, G.W., Bush, A.O. & Aho, J.M. (1990) Parasite communities: patterns and processes. 304 pp. New York, Chapman & Hall.Google Scholar
Frost, D.R., Rodrigues, M.T., Grant, T. & Titus, T.A. (2001) Phylogenetics of the lizard genus Tropidurus (Squamata: Tropiduridae: Tropidurinae): direct optimization, descriptive efficiency, and sensitivity analysis of congruence between molecular data and morphology. Molecular Phylogenetics and Evolution 21, 352371.CrossRefGoogle ScholarPubMed
Golberg, S.R. & Bursey, C.R. (1989) Helminths of the giant spotted whiptail, Cnemidophorus burti stictogrammus (Sauria: Teiidae). Proceedings of the Helminthological Society of Washington 56, 8687.Google Scholar
Golberg, S.R. & Bursey, C.R. (1990) Helminths of the Arizona little striped whiptail, Cnemidophorus inornatus arizonae, and the desert grassland whiptail, Cnemidophorus uniparens (Sauria: Teiidae), from southeastern Arizona. Journal of the Helminthological Society of Washington 57, 8386.Google Scholar
Golberg, S.R. & Bursey, C.R. (2003) Natural history notes. Cnemidophorus hyperythrus (orange-throated whiptail). Endoparasites. Herpetological Review 34, 142.Google Scholar
Golberg, S.R., Bursey, C.R. & Kraus, F. (2002) Seasonal variation in the helminth community of the brown anole, Anolis sagrei (Sauria: Polychrotidae), from Oahu, Hawaii. American Midland Naturalist 148, 409415.CrossRefGoogle Scholar
Gregory, R.D. & Keymer, A.E. (1989) The ecology of host-parasite interactions. Science Progress 73, 6780.Google ScholarPubMed
Huey, R.B. & Pianka, E.R. (1981) Ecological consequences of foraging mode. Ecology 62, 991999.CrossRefGoogle Scholar
Lent, H., Freitas, J.F.T. & Proença, M.C. (1946) Alguns helmintos de batraquios colecionados no Paraguai. Memórias do Instituto Oswaldo Cruz 44, 195214.CrossRefGoogle Scholar
Lyon, R.E. (1986) Helminth parasites of six lizard species from southern Idaho. Proceedings of the Helminthological Society of Washington 53, 291293.Google Scholar
McAllister, C.T. (1990a) Helminth parasites of unisexual and bisexual whiptail lizards (Teiidae) in North America. 1. The Colorado checkered whiptail (Cnemidophorus tesselatus) . Journal of Wildlife Diseases 26, 139142.CrossRefGoogle ScholarPubMed
McAllister, C.T. (1990b) Helminth parasites of unisexual and bisexual whiptail lizards (Teiidae) in North America. 2. The New Mexico whiptail (Cnemidophorus neomexicanus) . Journal of Wildlife Diseases 26, 403406.CrossRefGoogle ScholarPubMed
McAllister, C.T. (1990c) Helminth parasites of unisexual and bisexual whiptail lizards (Teiidae) in North America. 3. The Chihuahuan spotted whiptail (Cnemidophorus exsanguis) . Journal of Wildlife Diseases 26, 544546.CrossRefGoogle Scholar
McAllister, C.T. (1990d) Helminth parasites of unisexual and bisexual whiptail lizards (Teiidae) in North America. 4. The Texas spotted whiptail (Cnemidophorus gularis) . Texas Journal of Science 42, 381388.Google Scholar
McAllister, C.T. (1992) Helminth parasites of unisexual and bisexual whiptail lizards (Teiidae) in North America. 8. The Gila spotted whiptail (Cnemidophorus flagellicaudus), Sonoran spotted whiptail (Cnemidophorus sonorae), and Plateau striped whiptail (Cnemidophorus velox) . Texas Journal of Science 44, 233239.Google Scholar
McAllister, C.T., Cordes, J.E. & Walker, J.M. (1991a) Helminth parasites of unisexual and bisexual whiptail lizards (Teiidae) in North America. 6. The gray checkered whiptail (Cnemidophorus dixoni) . Texas Journal of Science 43, 309314.Google Scholar
McAllister, C.T., Trauth, S.E. & Conn, D.B. (1991b) Helminth parasites of unisexual and bisexual whiptail lizards (Teiidae) in North America. 7. The 6-lined racerunner (Cnemidophorus sexlineatus) . Texas Journal of Science 43, 391397.Google Scholar
Pereira, C. (1935) Os Oxyurata parasitos de Lacertilia do nordeste brasileiro. Archivos do Instituto Biológico, São Paulo 6, 527.Google Scholar
Ribas, S.C., Rocha, C.F.D., Teixeira-Filho, P.F. & Vicente, J.J. (1995) Helminths (Nematoda) of the lizard Cnemidophorus ocellifer (Sauria: Teiidae): assessing the effect of rainfall, body size and sex in the nematode infection rates. Ciência e Cultura 47, 8891.Google Scholar
Ribas, S.C., Rocha, C.F.D., Teixeira-Filho, P.F. & Vicente, J.J. (1998a) Nematode infection in two sympatric lizards (Tropidurus torquatus and Ameiva ameiva) with different foraging tactics. Amphibia-Reptilia 19, 323330.CrossRefGoogle Scholar
Ribas, S.C., Teixeira-Filho, P.F., Rocha, C.F.D. & Vicente, J.J. (1998b) Parasitismo por nematóideos em duas espécies simpátricas de Mabuya (Lacertilia: Scincidae) na restinga da Barra de Maricá, RJ. Anais do VIII Seminário Regional de Ecologia, São Carlos 883–894.Google Scholar
Rocha, C.F.D. (1995) Nematode parasites of the Brazilian sand lizard, Liolaemus lutzae . Amphibia-Reptilia 16, 412415.CrossRefGoogle Scholar
Rocha, C.F.D. (1996) Seasonal shift in lizard diet: the seasonality in food resources affecting the diet of Liolaemus lutzae (Tropiduridae). Ciência e Cultura 48, 264269.Google Scholar
Rocha, C.F.D. (2000) Biogeografia de répteis de restinga: distribuição, ocorrências e endemismos. pp. 99116 in Esteves, F.A. & Lacerda, L.D. (Eds) Ecologia de restingas e lagoas costeiras. Macaé, NUPEM/UFRJ.Google Scholar
Rocha, C.F.D., Bergallo, H.G. & Peccinini-Seale, D. (1997) Evidence of an unisexual population of the Brazilian whiptail lizard genus Cnemidophorus (Teiidae), with description of a new species. Herpetologica 53, 374382.Google Scholar
Rocha, C.F.D., Menezes, V.A. & Dutra, G.F. (1999) Geographical distribution Cnemidophorus nativo Herpetological Review 30 109.Google Scholar
Rocha, C.F.D. (2000) Biogeografia de répteis de restinga: distribuição, ocorrências e endemismos. pp. 99116 in Esteves, F.A. & Lacerda, L.D. (Eds) Ecologia de restingas e lagoas costeiras. Macaé, NUPEM/UFRJ.Google Scholar
Specian, R.D. & Whittaker, F.H. (1980) A survey of the helminth fauna of Cnemidophorus murinus from the island of Curaçao. Proceedings of the Helminthological Society of Washington 47, 275276.Google Scholar
Teixeira-Filho, P.F., Rocha, C.F.D. & Ribas, S.C. (2003) Relative feeding specialization may depress ontogenetic, seasonal and sexual variations in diet: the endemic lizard Cnemidophorus littoralis (Teiidae). Brazilian Journal of Biology 63, 321328.CrossRefGoogle ScholarPubMed
Telford, S.R. Jr, (1970) A comparative study of endoparasitism among some southern California lizard populations. American Midland Naturalist 83, 516554.CrossRefGoogle Scholar
Van Sluys, M., Rocha, C.F.D. & Ribas, S.C. (1994) Nematodes infecting the lizard Tropidurus itambere in southeastern Brazil. Amphibia-Reptilia 15, 405408.CrossRefGoogle Scholar
Van Sluys, M., Rocha, C.F.D., Bergallo, H.G., Vrcibradic, D. & Ribas, S.C. (1997) Nematode infection in three sympatric lizards in an isolated fragment of restinga habitat in southeastern Brazil. Amphibia-Reptilia 18, 442446.CrossRefGoogle Scholar
Vanzolini, P.E., Ramos-Costa, A.M.M. & Vitt, L.J. (1980) Repteis das caatingas. 161 pp. Rio de Janeiro, Academia Brasileira de Ciências.CrossRefGoogle Scholar
Vicente, J.J., Rodrigues, H.O., Gomes, D.C. & Pinto, R.M. (1993) Nematóides do Brasil. Parte III: Nematóides de Répteis. Revista Brasileira de Zoologia 10, 19168.CrossRefGoogle Scholar
Vicente, J.J., Van Sluys, M., Fontes, A.F. & Kiefer, M.C. (2000) Subulura lacertilia sp.n. (Nematoda, Subuluridae) parasitizing the Brazilian lizard Tropidurus nanuzae Rodrigues (Lacertilia, Tropiduridae). Revista Brasileira de Zoologia 17, 10651068.CrossRefGoogle Scholar
Vrcibradic, D., Rocha, C.F.D., Ribas, S.C. & Vicente, J.J. (1999) Nematodes infecting the skink Mabuya frenata in Valinhos, São Paulo State, southeastern Brazil. Amphibia-Reptilia 20, 333339.CrossRefGoogle Scholar
Vrcibradic, D., Cunha-Barros, M., Vicente, J.J., Galdino, C.A.B., Hatano, F.H., Van Sluys, M. & Rocha, C.F.D. (2000a) Nematode infection patterns in four sympatric lizards from a restinga habitat (Jurubatiba) in Rio de Janeiro state, southeastern Brazil. Amphibia-Reptilia 21, 307316.Google Scholar
Vrcibradic, D., Vicente, J.J. & Bursey, C.R. (2000b) Thubunaea dactyluris sensu Fabio and Rolas, a synonym of Physalopteroides venancioi (Spirurida, Physalopteridae). Journal of Parasitology 86, 11631165.CrossRefGoogle ScholarPubMed
Vrcibradic, D., Rocha, C.F.D., Bursey, C.R. & Vicente, J.J. (2002a) Helminths infecting Mabuya agilis (Lacertilia, Scincidae) in a ‘restinga’ habitat (Grumari) of Rio de Janeiro, Brazil. Amphibia-Reptilia 23, 109114.Google Scholar
Vrcibradic, D., Rocha, C.F.D., Bursey, C.R. & Vicente, J.J. (2002b) Helminth communities of two sympatric skinks (Mabuya agilis and Mabuya macrorhyncha) from two ‘restinga’ habitats in southeastern Brazil. Journal of Helminthology 76, 355361.CrossRefGoogle ScholarPubMed
Vrcibradic, D., Rocha, C.F.D. & Teixeira, R.L. (2002c) Geographic distribution Cnemidophorus nativo . Herpetological Review 33, 223.Google Scholar
Wright, J.W. (1993) Evolution of the lizards of the genus Cnemidophorus. pp. 2781 in Wright, J.W., Vitt, L.J. (Eds) Biology of whiptail lizards (genus Cnemidophorus). Norman, Oklahoma Museum of Natural History.Google Scholar
Zar, J.H. (1999) Biostatistical analysis. 4th edn. 663 pp. Upper Saddle River, Prentice Hall, Inc. Google Scholar