(Rodentia: Caviidae) by the tropical rattlesnake Crotalus durissus
Transcrição
(Rodentia: Caviidae) by the tropical rattlesnake Crotalus durissus
Herpetology Notes, volume 6: 277-279 (2013) (published online on 14 June 2013) Predation of the spix’s yellow-toothed cavy, Galea spixii (Rodentia: Caviidae) by the tropical rattlesnake Crotalus durissus cascavella (Serpentes: Viperidae) in the semi-arid region of Brazil Kariny de Souza1,2, Rafael Damasceno Fernandes Coelho1,2, Paulo Mauricio Almeida Guimarães Reis1,2, Patricia Avello Nicola1,2, Luiz Cezar Machado Pereira1,2 and Leonardo Barros Ribeiro1,2* The neotropical rattlesnake, Crotalus durissus, is distributed from southern Mexico to northern Argentina. The habitat of these snakes encompasses semi-arid regions, including dry and very dry tropical forests, thorn bushes and relatively dry open areas, in addition to a propensity to occupy areas degraded by human activity (Campbell and Lamar, 1989). Despite their wide geographic distribution, data on the natural history and ecology of this species are scarce (Sant’Anna and Abe, 2007). The main traits of genus Crotalus are solenoglyph fangs, presence of loreal pit and rattle at the tip of the tail. These viviparous terrestrial snakes, whose diet consists of vertebrates (Klauber, 1982), are predominantly nocturnal, and can be found in burrows and among debris (Martins and Oliveira, 1998). Crotalus durissus cascavella (Fig. 1) is a snake native of northeastern Brazil. Rodents of the genus Galea belong to the family Caviidae Gray, 1821, are endemic to South America (Woods, 1982; Solmsdorff et al., 2004) and popularly known as “preás” or “preás-do-campo” (spix’s yellowtoothed cavy). These rodents are characterized by their medium-sized body covered by hair ranging in color from gray to light brown, with body mass between 200 and 650 g, presence of periocular ring and absence of 1 Universidade Federal do Vale do São Francisco - UNIVASF, Campus Ciências Agrárias, CEP 56300-990, Petrolina, PE, Brasil. 2 Centro de Conservação e Manejo de Fauna da Caatinga (CEMAFAUNA-CAATINGA), Universidade Federal do Vale do São Francisco - UNIVASF, Rodovia BR 407, km 12, Lote 543, s/nº - C1, CEP 56300-990, Petrolina, PE, Brasil. * Corresponding author; e-mail: [email protected] a tail (Doutt, 1938; Díaz, 2000). They are terrestrial animals with diurnal habits, but sporadically active at night (Streilen, 1982a). Galea spixii (Fig. 2) is widely distributed throughout Brazil, from southeastern Pará to eastern Mato Grosso, northwestern Minas Gerais, western Bahia, Pernambuco, Paraíba and Rio Grande do Norte, southern Ceará, southcentral Piauí and Maranhão, in addition to the Federal Figure 1. An adult male rattlesnake, Crotalus durissus cascavella from the municipality of Cabrobó, Pernambuco, Brazil. Photo: L.B. Ribeiro. Figure 2. Adult specimen of spix’s yellow-toothed cavy, Galea spixii. Photo: CEMAFAUNA-CAATINGA. 278 Figure 3. Dissection of Crotalus durissus cascavella for removal of the stomach (top) and weighing of the snake’s stomach containing the rodent Galea spixii (bottom). Photos: P.M.A.G. Reis. District (Moojen, 1952). They also occur in Paraguay and Bolivia east of the Andes. Their habitat consists of rocky outcrops, lowland caatinga and cultivated fields in the Caatinga (Streilen, 1982b), as well as in areas of the Cerrado (Bonvicino, Oliveira and D’Andrea, 2008). Here, we report on the ingestion of G. spixii previously unrecorded as prey for C. d. cascavella in the Caatinga of north-eastern Brazil. On 20 December, 2012, during a herpetological expedition near the construction site of one of the water conduction canals, part of the Integration Project of the San Francisco River in the township of Cabrobó, Pernambuco state, a specimen of C. d. cascavella was found at 18:10 h among debris covered with cactus vegetation (08°30’22.25”S, 39°28’1.91”W; 351 m elev.). The snake was sighted after its presence was announced by warning calls emitted by a group of white-naped jays (Cyanocorax cyanopogon). The snake, which displayed dilated stomach region, was collected and taken to the Serpentarium of the Center for the Conservation and Kariny de Souza et al. Management of Caatinga Fauna (CEMAFAUNACAATINGA) in Petrolina, Pernambuco. The snake was euthanized on 26 September with inoculation of 5 ml of ketamine chloride (10%) associated with intraperitoneal administration of xylazine chloride (2%). At the Herpetology Laboratory we performed the morphometry, and the snake was 789.0 mm snout-vent length and total length of 815.8 mm. The specimen was determined to be a male by hemipenis exposure. Dissection (Fig. 3) revealed a subadult rodent in the stomach identified as G. spixii. It was ingested headfirst and was found in an advanced state of digestion. The head was partially decomposed, with the absence of a number of bones such as the zygomatics. The species was identified by analyzing cranial structures such as the maxillary bones and the molariform series anteriorly convergent, forming a “V” (Fig. 4). A deep external notch was also absent on the second prism of the PM (maxillary premolar), M1 (maxillary first molar) and M2 (maxillary second molar), typical of Cavia, a genus closely related with Galea (Rowe and Honeycutt, 2002). The prey exhibited total length of 264 mm, corresponding to 32.4% of total snake length. The weight of C. d. cascavella after stomach content removal was 360 g, and that of the stomach containing G. spixii was 152 g, such that the rodent corresponded to approximately 42% of snake body weight. Both were deposited in the Herpetological Collection of the Caatinga Fauna Museum at CEMAFAUNACAATINGA, under identification number MFCH 1841. Figure 4. Maxillary fragment of the spix’s yellow-toothed cavy, Galea spixii predated by Crotalus durissus cascavella, illustrating the molariform teeth converging previously forming a “V”. Photo: W. Lopes. Predation of the spix’s yellow-toothed cavy, Galea spixii (Rodentia: Caviidae) In a study by Sant’Anna and Abe (2007), of 343 prey items found in 259 C. durissus, 341 corresponded to mammals, rodents being the most frequent, with 40 unidentified Rodentia, one unidentified Caviid, and 223 Murids (Calomys sp. [99], Bolomys sp. [34], Oligoryzomys sp. [33], Rattus sp. [26], Mus musculus [12], Oryzomys sp. [4], Akodon sp. [12], Holochilus sp. [2], Pseudoryzomys sp. [1]). Complementing the total were 64 unidentified Mammalia, 13 Marsupialia Didelphidae and two teiid lizards (Ameiva ameiva). The highest occurrence of rodents as food items in rattlesnakes may be owing to its nocturnal activity, coincident with that of their prey. The record of predation on G. spixii by C. d. cascavella reported here suggests opportunistic predatory behavior, with the ingestion of a relatively large prey in relation to the snake’s size. This event may be due to the possibility of prey scarcity in the dry season and the guarantee of extensive fasting for the predator. Acknowledgements. We thank the Ministério da Integração Nacional for financial support, the Center for Conservation and Management of Caatinga Fauna (CEMAFAUNA-CAATINGA) for logistics support, and the Programa Institucional de Bolsas de Iniciação Científica (PIBIC) which is sponsored by the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for the research scholarship granted to K. Souza (Processes 103/2012 and 143744/2012-7). Collecting permits (Permit 95/2012 and Process 02001.003718/94-54) were granted by Instituto Brasileiro do Meio Ambiente e dos Recursos Naturais 279 Moojen, J. (1952): Os roedores do Brasil. Rio de Janeiro, Ministério da Educação e Saúde, Instituto Nacional do Livro. Rowe, D.L., Honeycutt, R.L. (2002): Phylogenetic relationships, ecological correlates, and molecular evolution within the Cavioidea (Mammalia: Rodentia). Molecular Biology and Evolution 19: 263-277. Sant’Anna, S.S., Abe, A.S. (2007): Diet of the rattlesnake Crotalus durissus in southeastern Brazil (Serpentes, Viperidae). Studies on Neotropical Fauna and Environment 42: 169-174. Solmsdorff, K., Kock, D., Hohoff, C., Sachser, N. (2004): Comments on the genus Galea Meyen, 1833 with description of Galea monasteriensis n. sp. from Bolivia (Mammalia, Rodentia, Caviidae). Senckenbergiana Biologica 84: 137-156. Streilen, K.E. (1982a): Ecology of small mammals in the semiarid Brazilian Caatinga. I. Climate and faunal composition. Annals of Carnegie Museum 51: 79-107. Streilen, K.E. (1982b): Ecology of small mammals in the semiarid Brazilian Caatinga. IV. Habitat selection. Annals of Carnegie Museum 51: 331-343. Woods, C.A. (1982): The history and classification of South American hystricognath rodents: reflections on the far away and long go. In: Mammalian Biology in South America, p. 377-392. Mares, M.A., Genoways, H.H., Eds., Pennsylvania, Special Publication, Pymatuning Laboratory of Ecology, University of Pittsburgh. Renováveis (IBAMA). References Bonvicino, C.R., Oliveira, J.A., D’Andrea, P.S.D. (2008): Guia dos roedores do Brasil, com chaves para gêneros baseadas em caracteres externos. Rio de Janeiro, Centro Pan-Americano de Febre Aftosa. Campbell J.A., Lamar W.W. (1989): The venomous reptiles of Latin America. Ithaca, Cornell University Press. Díaz, M.M. (2000): Key to the native mammals of Jujuy Province, Argentina. Occasional Papers, Sam Noble Oklahoma Museu of Natural History 7: 1-29. Doutt, J.K. (1938): Two new mammals from South America. Journal of Mammalogy 19: 100-101. Klauber, L.M. (1982): Rattlesnakes, their habits, life histories and influence on mankind. Berkeley, University of California Press. Martins, M., Oliveira, M.E. (1998): Natural history of snakes in forests of the Manaus region, Central Amazonia, Brazil. Herpetological Natural History 6: 78-150. Accepted by Philip de Pous
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