Predation by Kentropyx Calcarata Spix, 1825

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Herpetology Notes, volume 14: 1141-1143 (2021) (published online on 20 August 2021) Predation by Kentropyx calcarata Spix, 1825 (Squamata: Teiidae) on Physalaemus camacan Pimenta et al., 2005 (Anura: Leptodactylidae) in a mangrove area in northeastern Brazil Maurivan Vaz Ribeiro1,2,* and Alexandre Schiavetti1 Amphibians prey mainly on invertebrates and The Striped Forest Whiptail, Kentropyx calcarata are preyed on by lizards, snakes, birds, mammals, Spix, 1825 (Squamata: Teiidae) is a medium-sized invertebrates, as well as other amphibians (Walters, lizard (maximum SVL in males 119 mm, in females 1975; Vitt, 1991; Franzini et al., 2017). While 111 mm; Vitt, 1991) with a wide distribution in the mangrove environments function primarily as nursery eastern Amazon (eastern Venezuela, Guyana, French habitat for many fish species, some amphibian and Guiana, Suriname, Bolivia; Ávila-Pires, 1995; Uetz reptile species can also be found there (Kathiresan and et al., 2021). In Brazil, in addition to the Amazon Bingham, 2001; Roberto et al., 2012). Understanding region, it can be found in Atlantic Forest, Cerrado, the ecological functions of reptiles and amphibians in and Caatinga habitats (Avila-Pires, 1995; Sousa and mangroves is fundamental for the conservation of the Freire, 2008). It is a terrestrial, heliothermic species species that occupy these environments (Sandilyan and that inhabits mainly forested areas (Vitt, 1991; Vitt et Kathiresan, 2012), particularly since habitat loss due to al., 1997) and has excellent swimming skills (Roberto human invasion is a major factor causing the decline of et al., 2012) that the species uses as an escape strategy many species (Kathiresan and Bingham, 2001). when facing predators (Pianka and Vitt, 2003). Their Physalaemus camacan Pimenta et al., 2005 (Anura: diet consists mainly of arthropods (Vitt et al., 1997; Leptodactylidae) is an endemic foam frog species of Franzini et al., 2019). In mangrove environments, the Atlantic Forest and its distribution is restricted to crabs (family Grapsidae) have been reported as part southern Bahia State in Brazil (Frost, 2021). There of their diet (Roberto et al., 2012). Occasionally, it can is not much information about its natural history or also feed on other lizards (Franzini et al., 2017). biology available in the literature, with the exception of On 4 September 2020 at 10:36 h, we observed a its vocalization (Hepp et al., 2020) and the description predation event by K. calcarata on an individual of P. of its tadpole (Pimenta et al., 2005). For this reason, it is camacan in a mangrove swamp in Ilhéus Municipality, considered as Data Deficient (DD) by the International Bahia State, Brazil (14.6933°S, 39.0746°W). The Union for the Conservation of Nature (IUCN, 2021). observation took place in an area of hydromorphic This species is characterized by its medium size soil (Furukawa, 1996) that is characterized by (maximum snout–vent length, SVL, in males 24.1 mm, typical mangrove vegetation, such as Rhizophora in females 23.9 mm; Pimenta et al., 2005) compared mangle (Rhizophoraceae), Avicennia germinans to other, larger species in the Physalaemus signifier (Avicenniaceae), and Laguncularia racemosa group. So far, only a single predation event of this (Combretaceae) (Roberto et al., 2012; Gonçalves et species by a spider (Ctenus rectipes) has been reported al., 2017; Fig. 1A–C). On this occasion, the whiptail in the literature (Mira-Mendes et al., 2018). captured the frog on the ground and then took refuge in a bush (Fig. 1D). From this vantage point, it slapped the frog several times against the ground until it stopped struggling (Fig. 2). Subsequently, the whiptail 1 Laboratório de Etnoconservação e Áreas Protegidas, Universidade Estadual de Santa Cruz, Ilhéus, Bahia 45662- ingested the frog and ran off into the mangroves. The 900, Brazil. entire event lasted about 5 min. 2 Laboratório de Herpetologia Tropical, Universidade Estadual Mangrove environments act as nurseries and shelter de Santa Cruz, Ilhéus, Bahia 45662-000, Brazil. for many species and as a source of abundant prey for * Corresponding author. E-mail: [email protected] others (Laegdsgaard and Johnson, 1995). Recently, © 2021 by Herpetology Notes. Open Access by CC BY-NC-ND 4.0. the Brazilian federal government proposed to repeal 1142 Maurivan Vaz Ribeiro & Alexandre Schiavetti Figure 1. (A–D) Views of the characteristic mangrove environment in Ilhéus Municipality, Bahia State, northeastern Brazil, where the predation event took place. The red ellipse in (D) shows the place where the Striped Forest Whiptail, Kentropyx calcarata, took refuge to finish swallowing its prey, the foam frogPhysalaemus camacan. Photos by Tadeu Medeiros. resolution 303/2012 of the Conselho Nacional de Meio Frost, D.R. (2021): Amphibian Species of the World: an Online Ambiente, a rule that protects mangrove environments Reference. Version 6.1 (06 April 2021). Electronic Database (Menegassi, 2020), which ignited a warning about the accessible at https://amphibiansoftheworld.amnh.org/index. php. American Museum of Natural History, New York, USA. real human impacts on these environments for species Furukawa, K., Wolanski, E. (1996): Sedimentation in mangrove and their ecological relationships (Jin-Eong, 1995). forests. Mangroves and salt marshes 1(1): 3–10. Because of this, studies that aim to understand these Gonçalves, A.L., Cruz, V.M.S. da, Prazeres Campos, J.R. dos, aspects can provide important information for the Souza, D.V. (2017): Composição florística e fitossociológica conservation of mangroves. do manguezal da zona portuária de São Luís, Maranhão, Brasil. BIOFIX Scientific Journal 3(1): 01–07. Acknowledgments. We would like to thank Tadeu Medeiros Hepp, F. (2020): Review of bioacoustical traits in the genus for allowing us to use his pictures of mangroves, Daniela Pareja Physalaemus Fitzinger, 1826 (Anura: Leptodactylidae: Mejia for correction of the manuscript and Mirco Solé for a pre- Leiuperinae). Zootaxa 4725(1): 1–106. peer review. IUCN (2021): The IUCN Red List of Threatened Species. Version 2021-1. https://www.iucnredlist.org Jin-Eong, O. (1995): The ecology of mangrove conservation & References management. Hydrobiologia 295(1): 343–351. Avila-Pires, T.C.S. (1995): Lizards of Brazilian Amazonia Kathiresan, K., Bingham, B. L. (2001): Biology of mangroves and (Reptilia: Squamata). Zoologische Verhandelingen 299: 1–706 mangrove ecosystems. Advances in Marine Biology 40: 81–251. Franzini, L.D., Teixeira, A.A.M., Mesquita, D.O., Araújo, J.A. de, Laegdsgaard, P., Johnson, C.R. (1995): Mangrove habitats as Teles, D.A. (2017): Predation of Norops fuscoauratus (Duméril nurseries: unique assemblages of juvenile fish in subtropical & Bibron, 1837) by Kentropyx calcarata (Spix, 1825) in a mangroves in eastern Australia. Marine Ecology Progress remnant of Atlantic Forest. Herpetology Notes 10: 249–250. Series 126: 67–81. Franzini, D.L, Adonias, A.M., Tavares-Bastos, L., Vitt, L.J., Menegassi, D. (2020): Entenda como fica a proteção dos Mesquita, D.O. (2019): Autecology of Kentropyx calcarata manguezais e restingas sem a resolução do Conama. Jornal (Squamata: Teiidae) in a remnant of Atlantic Forest in eastern O Eco, Brasilia, 04 de Outubro de 2020. Available at: https:// South America. Journal of Herpetology 53(1): 209–217. www.oeco.org.br/reportagens/entenda-como-fica-a-protecao- dos-manguezais-e-restingas-sem-a-resolucao-do-conama. Predation by Kentropyx calcarata on Physalaemus camacan 1143 Figure 2. Predation of the foam frog Physalaemus camacan by the Striped Forest Whiptail, Kentropyx calcarata, in Ilhéus Municipality, Bahia State, northeastern Brazil. Photo by Maurivan Vaz Ribeiro. Mira-Mendes, C.V., Ruas, D.S., Oliveira, R.M. de, Castro, I.M., Uetz, P., Freed, P., Aguilar, R., Hošek, J., Eds. (2021): The Dias, I.R., Baumgarten, J.E., et al. (2018): Amphibians of the Reptile Database. Available at: http://www.reptile-database. Reserva Ecológica Michelin: a high diversity site in the lowland org. Accessed on 6 April 2021. Atlantic Forest of southern Bahia, Brazil. ZooKeys 1(753): 1–21. Vitt, L.J. (1991): Ecology and life history of the wide-foraging Pianka, E.R., Vitt, L.J. (2003): Lizards: Windows to the Evolution lizard Kentropyx calcarata (Teiidae) in Amazonian Brazil. of Diversity. Berkeley, California, University of California Press. Canadian Journal of Zoology 69: 2791–2799. Pimenta, B., Silvano, D., Cruz, C.A.G. (2005): A new Vitt, L.J., Zani, P.A., Lima, C.M. (1997): Heliotherms in tropical species of the genus Physalaemus Fitzinger, 1826 (Anura, rain forest: the ecology of Kentropyx calcarata (Teiidae) and Leptodactylidae) from the Atlantic Rain Forest of southern Mabuya nigropunctata (Scincidae) in the Curuá-Una of Brazil. Bahia, Brazil. Amphibia-Reptilia 26(2): 201–210. Journal of Tropical Ecology 13: 199–220. Roberto, I.J., Brito, L., Pinto, T. (2012): Ecological aspects of Walters, B. (1975): Studies of interspecific predation within an Kentropyx calcarata (Squamata: Teiidae) in a mangrove area amphibian community. Journal of Herpetology 1975: 267–279. in northeastern Brazil. Boletín de la Asociación Herpetológica Española 23(1): 3–8. Sandilyan, S., Kathiresan, K. (2012): Mangrove conservation: a global perspective. Biodiversity and Conservation 21(14): 3523–3542. Accepted by Christoph Liedtke Sousa, P.A.G., Freire, E.M.X. (2008): Geographic distribution. Kentropyx calcarata. Herpetological Review 39: 238..
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    742 NATURAL HISTORY NOTES farther than where the fruit had fallen, would make D. roquet ze- Norval et al. 2012. Herpetol. Notes 5:451–452; Herman 2013. Her- brila a relatively poor disperser of E. havanense. petol. Rev. 45:203–205; Hecnar and Hecnar 2018. Herpetol. Rev. THOMAS BILLE, Holmegaardsvej 90A, 4684 Holmegaard, Denmark; 47:108–109) and it can be an important conservation issue when e-mail: [email protected]. long distances are involved (Davis et al. 2011. Nature 474:153–154) and exotic species become established (Meshaka et al. 2004. The ENYALIUS BILINEATUS (Two-lined Fat-headed Anole). DEFEN- Exotic Amphibians and Reptiles oF Florida, KrieGer PublishinG, SIVE BEHAVIOR. Enyalius bilineatus is a species of semi-arbore- Malabar, Florida. 166 pp.). al lizard with a distribution in the southeastern, central-western, On 8 April 2018, a Gecko (ca. total lenGth = 12 cm) emerGed From and northeastern regions of Brazil (Rodrigues et al. 2014. Mol. the external mirror housing of a Jeep being towed by a Winnebago Phylogenet. Evol. 81:137–146; Sales et al. 2015. Brazil. Check List motorhome just after it arrived at a family campground near Grand J. Biodivers. 11:10–12). Defensive behaviors of E. bilineatus re- Bend, Ontario (43.2574°N, 81.8033°W; WGS 84). The motorhome main largely unknown. Here we report the types and frequency was driven from Winter Haven, Florida where the owners spent of defensive behaviors made by E. bilineatus upon capture. This the winter (28.0333°N, 81.7167°W; WGS 84) and covered a road study took place at the National Forest of Ritápolis (21.05586°S, distance of 2080 km (ca.
  • Herpetological Journal FULL PAPER

    Herpetological Journal FULL PAPER

    Volume 26 (April 2016), 119–130 FULL PAPER Herpetological Journal Published by the British Reproductive biology of the southernmost Kentropyx Herpetological Society lizard from the Wet Chaco of Corrientes, Argentina Martín A. Ortiz1, Jorgelina M. Boretto2 & Nora R. Ibargüengoytía2 1Laboratorio de Herpetología, Facultad de Ciencias Exacta y Naturales y Agrimensura, Universidad Nacional del Nordeste, Av. Libertad 5460, ZIP Code: 3400. Corrientes, Argentina 2INIBIOMA (CONICET – Universidad Nacional del Comahue), San Carlos de Bariloche, ZIP Code: 8400, Río Negro, Argentina Studies on reproductive modes, size at maturity, clutch size and clutch frequency have contributed greatly to our understanding of life history variation among lizard populations, and thereby, to implement conservation strategies. Herein, we studied the reproductive biology of the vulnerable tegu lizardKentropyx viridistriga from Corrientes, northeastern Argentina (Wet Chaco). Kentropyx viridistriga are active from early summer to late autumn, with temperature and photoperiod influencing the timing of reproduction and the brumation period. Females showed an annual reproductive cycle, and males exhibited a continuous reproductive cycle during the activity season. Females laid at least two clutches of on average three eggs per reproductive season. Neonates occured in spring, and reached sexual maturity in the first year of life. Females reached sexual maturity at a larger snout-vent length (64.1 mm) than males (54.8 mm). Sexual dimorphism is evident, with males showing greater
  • And Imantodes Lentiferus (Serpentes: Dipsadidae) from Southeast Peru

    And Imantodes Lentiferus (Serpentes: Dipsadidae) from Southeast Peru

    Phyllomedusa 15(1):69–73, 2016 © 2016 Universidade de São Paulo - ESALQ ISSN 1519-1397 (print) / ISSN 2316-9079 (online) doi: http://dx.doi.org/10.11606/issn.2316-9079.v15i1p69-73 Short CommuniCation Notes on the reproduction of Kentropyx altamazonica (Squamata: Teiidae) and Imantodes lentiferus (Serpentes: Dipsadidae) from southeast Peru Shirley Jennifer Serrano Rojas1, 2, Jaime Villacampa1, and Andrew Whitworth3 1 The Crees Foundation, Mariscal Gamarra, B-5, Zona-1, 2da Etapa, Cusco, Peru. E-mail: [email protected] 2 Universidad Nacional de San Antonio Abad del Cusco (UNSAAC), Peru. E-mail: [email protected] 3 Institute of Biodiversity, Animal Health and Comparative Medicine, College of Medical, Veterinary and Life Sciences, University of Glasgow, G12 8QQ, Glasgow, United Kingdom. Keywords: Amazonia, clutch size, communal nesting, hatching, incubation, Manu Biosphere Reserve, oviposition. Palavras-chave: Biosfera Manu, tamanho da ninhada. Field observations on the reproductive lentiferus (Cope, 1894). Neither species has been biology of squamate reptiles are important to assessed by the International Union for understanding the life history, ecology, and Conservation of Nature (IUCN) Red List. evolution of this diverse group (Vitt 1991, Imantodes lentiferus, the Amazon Basin tree Ramírez-Bautista et al. 2000, Vitt et al. 2001, snake, is an arboreal and nocturnal dipsadid. It Werneck et al. 2009); however, these data occurs in lowland rainforest of the Amazon remain sparse for many tropical species (Figueroa Basin and Guiana region, having been reported et al. 2013, Sousa et al. 2014). Seasonality, from French Guiana, Suriname, Guyana, clutch frequency, clutch size, egg size, and body Venezuela, Colombia, Ecuador, Peru, Bolivia, size are important factors related to the life and Brazil (Frota et al.