Abstract
Home range is defined as the area within which an individual moves to acquire resources necessary to increase their fitness and may vary inter and intra-specifically with biotic and abiotic factors. This study details the home range of the parthenogenic lizard, Aspidoscelis cozumela, an active forager microendemic to Cozumel Island, México, with high preference for open sand beaches. The home range of A. cozumela was compared with other species of Aspidoscelis (gonochoric and parthenogenetic) and other lizards that occupy coastal habitats. Furthermore, the biotic and abiotic factors that may influence home range were analyzed. This study was conducted in the beach located on the East side of the island (area of 4 000 m2) that is composed primarily of halophyte vegetation with high levels of sunlight. From 1999 to 2001, nine samples were taken which included the dry, rainy, “nortes”, and breeding seasons. During each sampling, capture-mark-recapture techniques were conducted and the date, time of day, and snout-vent length (SVL) were recorded to the nearest millimeter. Individuals were located in the study area using a bi-coordinate reference using 10 x 10 m subdivisions of the habitat. Home range and home range overlap were calculated using the convex polygon method in McPaal and home range/SVL correlation was tested using Pearson´s correlation. To calculate females home range, three or more recaptures were considered. A total of 20 home ranges that averaged 45.1 ± 14.0 m2 were obtained and no correlation between SVL and home range size was detected (p = 0.9229, n = 20). However, removing individuals with outlier home ranges (females with home ranges > 100 m2, n = 2) resulted in a positive correlation with SVL (r = 0.61, p = 0.0072, n = 18). A 22.9 ± 5.7% overlap in home range was also detected. The small home range of A. cozumela represents the smallest home range within the Aspidoscelis genus recorded to date (including both parthenogenetic and gonochoric species) and contrasts the theoretical predictions of broad home ranges for widely foraging species. Thermoregulatory benefits and a high population density may explain the small home range of A. cozumela. Although this species is highly adapted to the environmental conditions present on the open sand beaches, anthropogenic effects on these habitats by the development of tourism infrastructure may jeopardize their existence on Cozumel Island.
References
Borges-Landáez, P., & Shine, R. (2003). Influence of toe-clipping on running speed in Eulamprus quoyii, an Australian scincid lizard. Journal of Herpetology, 37, 592-595.
Cuarón, A. D., Martínez-Morales, M. A., McFadden, K. W., Valenzuela, D., & Gompper, M. E. (2004). The status of dwarf carnivores on Cozumel Island, Mexico. Biodiversity and Conservation, 13, 317-331.
Díaz de la Vega Pérez, A. H., Jiménez-Arcos, V. H., Manríquez -Morán, N. L., & Méndez De la Cruz, F. R. (2013). Conservatism of thermal preferences between parthenogenetic Aspidoscelis cozumela complex (Squamata:Teiidae) and their parental species. Herpetological Journal, 23, 93-104.
Dirzo, R., Young, H. S., Galetti, M., Ceballos, G., Isaac, N. J. B., & Collen, B. (2014). Defaunation in the Anthropocene. Science, 345, 401-406.
Eifler, D. A. (1996). Experimental manipulation of spacing patterns in the widely foraging lizard Cnemidophorus uniparens. Herpetologica, 52, 477-486.
Elizalde-Rocha, S. P. (2007). Evolución y sistemática de las lagartijas partenogenéticas del género Aspidoscelis (Squamata: Teiidae) de la Península de Yucatán. (Tesis inédita de licenciatura). Universidad Autónoma del Estado de México. Toluca, Estado de México, México.
Elizalde-Rocha, S. P., Méndez De la Cruz, F. M., Méndez-Sánchez, J. F., Granados-González, G., & Hernández-Gallegos, O. (2008). Variación morfológica de la lagartija partenogenética Aspidoscelis rodecki (Squamata: Teiidae): Implicaciones evolutivas y de conservación. Revista de Biología Tropical, 56, 1871-1881.
Escobar-Nava, A. (1986). Geografía general del estado de Quintana Roo. México: Estado de Quintana Roo.
Flores-Villela, O. (1993). Herpetofauna Mexicana. Carnegie Museum of Natural History, 17, 1-73.
Galoyan, E. (2013). Joint space use in a parthenogenetic Armenian rock lizard (Darevskia armeniaca) suggests weak competition among monoclonal females. Journal of Herpetology, 47, 97-104.
García, E. (2004). Modificaciones al sistema de clasificación climática de Koppen. México: Universidad Nacional Autónoma de México.
Gómez-Ramírez, M. (1998). Ciclones tropicales que entraron a la Península de Yucatán de 1970 a 1995. Revista Geográfica, 124, 153-171.
Gómez-Ramírez, M. & Reséndiz-Espinosa, I. N. (2002). Seguimiento de nortes en el litoral del Golfo de México en la temporada 1999-2000. Revista Geográfica, 131, 5-19.
Gutiérrez, A. & Ortega, A. (1985). Comparación de métodos para calcular el área de actividad de Sceloporus scalaris. Acta Zoológica Mexicana, 12, 1-12.
Haenel, G. J., Smith, L. C., & John Alder, H. B. (2003). Home-range analysis in Sceloporus undulatus (Eastern Fence Lizard). I. Spacing patterns and the context of territorial behavior. Copeia, 99-112.
Hernández-Gallegos, O., Manríquez-Morán, N., Méndez, F. R., Villagrán, M., & Cuellar, O. (1998). Histocompatibility in parthenogenetic lizards of the Cnemidophorus cozumela complex from the Yucatán Peninsula of Mexico. Biogeographica, 74, 117-124.
Hernández Gallegos, O. (2004). Demografía de los lacertilios del complejo Aspidoscelis (Cnemidophorus) cozumela (Sauria: Teiidae) y sus especies parentales, en la Península de Yucatán, México. (Tesis inédita de doctorado). Universidad Nacional Autónoma de México, México, D. F.
Hirth, H. F. (1963). The ecology of two lizards on a tropical beach. Ecological Monographs, 33, 83-112.
Howell, S., & Webb, S. (1995). A guide to the birds of Mexico and Northern Central America. New York, USA: Oxford University Press.
Hulse, A. C. (1981). Ecology and reproduction of the parthenogenetic lizard Cnemidophorus uniparens (Teiidae). Annals of the Carnegie Museum of Natural History, 50, 353-369.
Jorgensen, C. D., & Tanner, W. W. (1963). The application of the density probability function to determine the home ranges of Uta stansburiana stansburiana and Cnemidophorus tigris tigris. Herpetologica, 19, 105-115.
Kacoliris, F. P., Williams, J. D., Ruiz De Arcaute, C., & Cassino, C. (2009). Home range size and overlap in Liolaemus multimaculatus (Squamata: Liolamidae) in Pampean coastal dunes of Argentina. South American Journal of Herpetology, 4, 229-234.
Konrad, H. W. (1996). Caribbean tropical storms: Ecological implications for prehispanic and contemporary Maya subsistence practice on the Yucatán Peninsula. Revista Mexicana del Caribe, 1, 98-130.
Lee, J. C. (1996). The amphibians and reptiles of the Yucatán Peninsula. Ithaca, USA: Cornell University Press.
Lewis, A. R., & Saliva, J. E. (1987). Effects of sex and size on home range, dominance and activity budgets in Ameiva exsul (Lacertilia: Teiidae). Herpetologica, 43, 374-383.
López-González, C. A., & González-Romero, A. (1997). The lizard community from Cozumel Island, Quintana Roo, Mexico. Acta Zoologica Mexicana, 72, 27-39.
López-Moreno, A. E. (2008). Ámbito hogareño de dos lagartijas partenogenéticas de la Península de Yucatán. (Tesis inédita de licenciatura). Universidad Autónoma del Estado de México, Toluca, Estado de México, México.
Manríquez-Morán, N. L., Villagrán Santa Cruz, M., & Méndez De la Cruz, F. R. (2000). Origin and evolution of the parthenogenetic lizards, Cnemidophorus maslini and C. cozumela. Journal of Herpetolology, 34, 634-637.
Manríquez-Morán, N. L. (2002). Origen y diversidad clonal en las especies de lagartijas partenogenéticas del complejo Cnemidophorus cozumela (Reptilia: Teiidae). (Tesis inédita de doctorado). Universidad Nacional Autónoma de México, México, D. F.
Manríquez-Morán, N. L., Villagrán Santa Cruz, M., & Méndez De la Cruz, F. R. (2005). Reproductive biology of the parthenogenetic lizard, Aspidoscelis cozumela. Herpetologica, 61, 435-439.
Manríquez-Morán, N. L., & Méndez De la Cruz, F. R. (2008). Genetic homogeneity between two populations of the parthenogenetic lizard Aspidoscelis cozumela. Revista Mexicana de Biodiversidad, 79, 421-426.
Manríquez Morán, N. L., Méndez De la Cruz, F. R., & Murphy, R. W. (2014). Genetic Variation and origin of parthenogenesis in the Aspidoscelis cozumela Complex: Evidence from mitochondrial genes. Zoological Science, 31, 14-19.
Martínez-Morales, M. A. (1999). Conservation status and habitat preferences of the Cozumel Curassow. Condor, 101, 11-20.
McCoy, C. J. (1965). Life history and ecology of Cnemidophorus tigris septentrionalis. (Ph.D. Thesis). University of Colorado, Boulder, Colorado, USA.
Menezes, V. A., & Rocha, C. F. D. (2013). Geographic distribution, population densities and issues on conservation of whiptail lizards in restinga habitats along the eastern coast of Brazil. North-Western Journal of Zoology, 9, 337-344.
Mitchell, J. C. (1979). Ecology of southeastern Arizona whiptail lizards (Cnemidophorus: Teiidae): population densities, resource partitioning and niche overlap. Canadian Journal of Zoology, 57, 1487-1499.
Morales-Mávil, J. E., Vogt, R. C., & Gadsden-Esparza, E. (2007). Desplazamientos de la iguana verde, Iguana iguana (Squamata: Iguanidae) durante la estación seca en La Palma, Veracruz, México. Revista de Biología Tropical, 55, 709-715.
Paulissen, M. A., & Meyer, H. A. (2000). The effects of toe-clipping on the gecko Hemidactylus turcicus. Journal of Herpetology, 34, 282-285.
Pianka, E. R. (1966). Convexity, desert lizards and spatial heterogeneity. Ecology, 47, 1055-1059.
Perry, G., & Garland, T. (2002). Lizard home ranges revisited: effects of sex, body size, diet, habitat and phylogeny. Ecology, 83, 1870-1885.
Reeder, T. W., Cole, C. J., & Dessauer, H. C. (2002). Phylogenetic relationships of whiptail lizards of the genus Cnemidophorus (Squamata: Teiidae): A test of monophyly, reevaluation of karyotypic evolution and review of hybrid origins. American Museum Novitates, 3365, 1-61.
Rocha, C. F. D. (1999). Home range of the tropidurid lizard Liolaemus lutzae: Sexual and body size differences. Revista Brasiliera de Biologia, 59, 125-130.
Rose, B. (1982). Lizard home ranges: Methodology and functions. Journal of Herpetology, 16, 253-269.
Rowland, S. D. (1992). Activity, behavior, ecology and home range of the orange-throated whiptail, Cnemidophorus hyperythrus beldingi Cope. (Master´s Thesis). California State University, Fullerton, California, USA.
Ruby, D. E. (1978). Seasonal changes in the territorial behavior of the iguanid lizard Sceloporus jarrovi. Copeia, 430-438.
Ruby, D. E., & Dunham, A. E. (1987). Variation in home range size along an elevational gradient in the iguanid lizard Sceloporus merriami. Oecologia, 71, 473-480.
Sánchez, O. (2011). Evaluación y monitoreo de poblaciones silvestres de reptiles. In O. Sánchez, P. Zamorano, E. Peters, & H. Moya (Eds.), Temas sobre conservación de vertebrados silvestres en México (pp. 83-120). D. F., México: Secretaría de Medio Ambiente y Recursos Naturales.
Schoener, T. W., & Schoener, A. (1982). The ecological correlates of survival in some Bahamian Anolis lizards. Oikos, 39, 1-16.
Stamps, J. A. (1983). Sexual selection, sexual dimorphism and territoriality. In R. B. Huey, E. R. Pianka, & T. W. Schoener (Eds.), Lizard Ecology: studies of a model organism (pp. 169-204). Massachusetts, USA: Harvard University Press.
Stüwe, M., & Blohowiak, C. E. (1985). Micro-computer programs for the analysis of animal locations (MACPAAL, version 1.2). Washington, DC, USA: Smithsonian Institution.
Taylor, H. L., & Cooley, C. R. (1995). A multivariate analysis of morphological variation among parthenogenetic Teiid lizards of the Cnemidophorus cozumela complex. Herpetologica, 51, 67-76.
Téllez-Valdez, O., Cabrera-Cano, E. F., Linares-Mazari, E., & Bye, R. (1989). Las plantas de Cozumel. México: Instituto de Biología, Universidad Nacional Autónoma de México.
Tinkle, D. W. (1967). The life and demography of the side blotched lizard Uta stansburiana. Miscellaneous Publications, Museum of Zoology, University of Michigan, 132, 1-182.
Verwaijen, D., & Van Damme, R. (2008). Wide home ranges for widely foraging lizards. Zoology, 111, 37-47.
Vitt, L. J., & Breitenbach, G. L. (1993). Life histories and reproductive tactics among lizards in the genus Cnemidophorus (Sauria: Teiidae). In J. W. Wright, & L. J. Vitt (Eds.), Biology of whiptail lizards (Genus Cnemidophorus) (pp. 211-244). Oklahoma, USA: Oklahoma Museum of Natural History.
Vitt, L. J., Zani, P. A., Caldwell, J. P., & Durtsche, R. D. (1993). Ecology of the whiptail lizard Cnemidophorus deppii on a tropical beach. Canadian Journal of Zoology, 71, 2391-2400.
Wilson D. E., & Reeder D. M. (1993). Mammal species of the world: A taxonomic and geographic reference. Washington, DC, USA: Smithsonian Institution Press.
Wright, J. W. (1993). Evolution of whiptail lizards (Genus Cnemidophorus). In J. W. Wright, & L. J. Vitt (Eds.), Biology of whiptail lizards (Genus Cnemidophorus) (pp. 27-82). Oklahoma, USA: Oklahoma Museum of Natural History.
Yáñez-Arancibia, A., & Day, J. W. Jr. (1988). Ecological characterization of Terminos Lagoon, a tropical lagoon-stuarine system in the southern Gulf of Mexico. In A. Yáñez-Arancibia & J. W. Day, Jr. (Eds.), Ecología de los ecosistemas costeros en el sur del Golfo de México: La región de la Laguna de Términos (pp. 1-40). México: Universidad Nacional Autónoma de México y Organización de los Estados Americanos.
Comments
This work is licensed under a Creative Commons Attribution 4.0 International License.
Copyright (c) 2015 Revista de Biología Tropical