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Natural History Notes of Wildlife Conservation, Sri Lanka. The PATAGONIENSIS (Parelheira): observations form part of Project Knuckles which VENOMOUS (CROTALID) AS PREY . was partly operated and partly funded by the is found almost University of Edinburgh, Scotland and organised everywhere in . In , it can be by Suraj Goonewardene and Anslem De Silva. found in the states of Pernanbuco and Bahia (Northeast Region), Minas Gerais, Rio de Janeiro and São Paulo (Southeast Region) and in Parana REFERENCES and Rio Grande do Sul (South Region) (Peters & Andrews, H. V. (1995). Sexual maturation in Orejas-Miranda, 1986) where it occurs primarily Varanus salvator (Laurenti, 1768), with notes in open areas, but also woodland (Thomas, 1976). on growth and reproductive effort. Herpetol. Philodryas patagoniensis is a medium-sized J. 5, 189–194. colubrid snake (Figure 1.) with predominantly Bennett, D. (1998). Monitor ; Natural terrestrial, diurnal habits (Marques et al ., 2001) History, Biology and Husbandry. Edition that feeds on frogs, lizards, , mice, and other Chimaira, Andreas S. Brahm: Frankfurt am (Duarte & Eterovic, 2003; Perroni, 2004; Main. Hartmann & Marques, 2005). However, available Horn, H. G. (1999). Evolutionary efficiency reports limit it to the ingestion of colubrids, such and success in monitors: a survey on as , Thamnodynastes strigatus, behaviour and behavioural strategies and Clelia occipitolutea, poecilogyrus, some comments. In: Advances in Monitor Liophis jaegeri , Helicops carinicaudus, Lystrophis Research II . Horn, H. & Bohme, W (Eds.). dorbignyi (Lema et al ., 1983) and Liophis Mertensiella 11, 167–180. poecilogyrus and Pseudablabes agassizii Horne, H.G., Gaulke, M. & Bohme, W. (1994). (Hartmann & Marques, 2005). Perroni (2004) New data on ritualised combats in monitor found dorsal and ventral scales of a non-identified lizards (Sauria: Varanidae) with remarks on colubrid on his analysis. According to Shine their function and phylogenetic implications. (1991) ophiophagus snakes can possibly show Zool. Garten N.F . 64, 265–280. cannibalism. In the Philodryas this has been Jolley, E. & Meek. R. (2006). Natural History confirmed by Lema (1983) and by Hartmann & Note. Varanus bengalensis (Bengal monitor): Marques (2005), with one report of cannibalism Unusual behaviour and feeding. Herpetol. each. In captivity, a newborn P. patagoniensis was Bull. 95, 31- 32. observed ingesting another conspecific newborn Rese, R. (1986). Der Kommentkampf bei by attacking and ingesting it head-first . Philodryas Varanus salvator . Sauria 8, 27–29. olfersii, despite being a non-, has Wicker, R., Gaulke, M. & Horn, H.G. (1999). enlarged maxillary fangs in addition to a Contributions to the biology, keeping and Duvernoy`s gland (which produces toxic breeding of the Mindanao Water Monitor substances), and is thus potentially bale to (Varanus s. cumingi ). In: Advances in envenomate its prey (Silvia Cardoso, personal Monitor Research II . Horn, H. & Bohme, W. observation). (Eds.). Mertensiella 11, 213–223. We analyzed gut contents from the digestive tract of one female Philodryas patagoniensis sent to us on April 24 th 2003 from Santana de Parnaíba 1 2 EDIE JOLLEY and ROGER MEEK - SP (23° 26’S. 46° 56’W), measuring 525 mm in 1 16 Mountfields, Halifax, West Yorkshire, U. K . snout-vent length (SVL), 190 mm in tail length Email: [email protected] (TL), 14.2 mm in head length (HL) and weighing 35 g. After examining the feaces of this individual, 2 7 Rue Georges Clemenceau, Chasnais, France . we verified the presence of a grooved fang which E-mail: [email protected] belonged to a venomous snake, probably a young

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Figure 1. Philodryas patagoniensis (adult female). © S. seriously considered the possibility of secondary R. Travaglia-Cardoso. prey ingestion but conclude that for several one. By comparing it with the fangs of other reasons this seems unlikely. Firstly it is known that venomous snakes born in captivity, in order to P. patagoniensis feeds primarily on mice and birds, estimate the age group of the swallowed prey item, and venomous snakes are not part of the general we found that it was from a of pit viper diet of these . In addition, only a large- (juvenile), probably of the genus . The sized could presumably have attacked a offspring of Bothrops spp. in Brazil are usually venomous snake, much larger than could have born between November and March (Almeida- been ingested by a Philodryas. Santos & Salomão, 2002), thus, on a newborn specimen by Philodryas patagoniensis in REFERENCES April could be possible. As far as we are aware Almeida-Santos, S. M. & Salomão, M. G. (2002). there are no other such records available in the Reproduction in neotropical pitvipers, with literature. Perhaps P. patagoniensis avoids this emphasis on species of the genus Bothrops . In: kind of prey because it is a venomous snake and Biology of the Vipers , pp. 445–462. Schuetti, G. can suffer some injury or even death . W., Hoggren, M., Douglas, M. E., & Greene, H. W. Alternatively, the snake may have been ingested (Eds.). Texas: Eagle Mountain publishing, LC. when already dead. No cases of feeding on carrion Duarte, M. R. & Eterovic, A. (2003). Serpentes have previously been reported for this species, but exóticas no Brasil. In: Animais Peçonhentos do it is rare to observe this kind of behaviour in nature Brasil: Biologia, Clínica e Terapêutica dos unless you see the snake directly encountering a Acidentes , pp. 13 –32. Cardoso, J. L. C., França, F. dead (Lillywhite, 1982; Shine, 1986). We O. S., Wen, F. H., Malaque, C. M. S., & Haddad,

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V. Jr. (Eds.). São Paulo: Ed. Sarvier. AMPHIESMA STOLATUM (Striped keelback): Hartmann, P .A. & Marques, O. A. V. (2005). Diet PREDATION ON POLYPEDATES and use of two sympatric species of MEGACEPHALUS (Java treefrog) . Snakes Philodryas (), in South Brazil. have solved the problem of nourishing a heavy Amphibia-Reptilia 26, 25 –31. body, with a relatively small mouth, b y Lema, T. Araújo, & M. L. Azevedo, A. C. P. (1983). infrequently consuming large prey items (Greene, Contribuição ao conhecimento da alimentação e 1997); made possible by the mobility of the jaw do modo alimentar de serpentes do Brasil. Com. and mouth skeleton (Ernst & Zug, 1996). But Mus. Ci. Tecnol. PUC-RS. Zool. Serie . 26, 64-65. preying on large prey comes at a cost. Snakes are not always capable of subduing such prey, and Lillywhite, H. B. (1982). Cannibalistic carrion even when they do, risk losing it due to other ingestion by the rattlesnake, Crotalus viridis . J. predators, as well as being subjected to the risk of Herpetol . 16, 95. predation themselves. Another problem is that Marques, O. A. V., Eterovic, A., Sazima, I. (2001). consuming a large prey item might result in injury Serpentes da Mata Atlântica: Guia Iilustrado Para or death to the snake due to the ingesting process Serra do Mar . Ribeirão Preto. Ed. Holos. or compromised mobility. It is thus crucial to note Perroni, L. P. G. (2004). Análise da morfometria e which prey items are consumed by which snake da dieta de Philodryas olfersii e Philodryas species, as well as the size of the prey in relation patagoniensis (Serpentes: Colubridae) da grande to the predator. Since the ability of snakes to São Paulo. Monografia de conclusão de curso. – swallow relatively large prey items is not equal Universidade Metodista de São Paulo. São Paulo. throughout the snake kingdom (Mattison, 1995), it Peters, J. A. & Orejas-Miranda, B. (1986). is important to note the prey/predator weight-ratio, Catalogue of the Neotropical : part I, and types of prey consumed by individuals of the snakes . Revised edition (originally published same species to develop a better understanding of 1970), addenda and corrigenda by P. E. Vanzolini. the energy budgets and foraging behaviour of the Washington: Smithsonian Institution. 347 pp. species in question. Shine, R. (1986). Ecology of a low-energy Here we report predation by a Striped keelback specialist: food habits and reproductive biology of (Amphiesma stolatum ) on a Java treefrog th the arafura filesnake (Acrochordidae). Copeia (Polypedates megacephalus ). At 11:52 h on 19 [S.l.] 2, 424 –437. May 2006, a male A. stolatum (430 mm SVL, 7.72 mm HW, 18 mm HL, 144 mm tail length, 13.2 g) Shine, R. (1991). Australian Snakes: A Natural was observed moving along the fence on the inside History . Ithaca: Cornell University Press. of a 6m x 6m enclosure, constructed of 3 mm Thomas, R. A. (1976). A revision of the American plastic mesh, erected in a Betelnut palm ( Areca colubrid snake genus Philodryas Wagler, 1830. catechu ) plantation in Santzepu, Sheishan District, Texas: Graduate College of Texas A and M Chiayi County, Taiwan (23º28’23”N, University. Unpublished thesis (Ph.D.). 338 pp. 120º29’15”E). The vegetation on the inside of the enclosure was very dense and consisted of A. LUIS PAULO GODA PERRONI 1 and SILVIA catechu , Bidens pilosa var. radiata , Ipomoea REGINA TRAVAGLIA-CARDOSO 2 cairica , Mikania micrantha , and Panicum maximum . The A. stolatum was captured and it 1 Museu Biológico, Instituto Butantan, Av. Vital was noted that the mid-body was greatly enlarged. Brazil, 1500, CEP 05503-900, São Paulo, SP, After gentle palpation of the enlarged area of the Brazil. mid-body, the snake regurgitated an anuran, along E-mail: [email protected] with a large number of eggs. The prey item was 2 Laboratório de Herpetologia, Instituto Butantan, identified as a female P. megacephalus (ca. 55 mm Av. Vital Brazil, 1500, CEP 05503- 900, São SVL, 2.5 g). Since it was regurgitated head and Paulo, SP, Brazil . fore limbs first, and the hind limbs folded forward, E-mail: [email protected] combined by the fact that the vent area and parts of

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