De Los Reptiles Del Yasuní

Total Page:16

File Type:pdf, Size:1020Kb

De Los Reptiles Del Yasuní guía dinámica de los reptiles del yasuní omar torres coordinador editorial Lista de especies Número de especies: 113 Amphisbaenia Amphisbaenidae Amphisbaena bassleri, Culebras ciegas Squamata: Serpentes Boidae Boa constrictor, Boas matacaballo Corallus hortulanus, Boas de los jardines Epicrates cenchria, Boas arcoiris Eunectes murinus, Anacondas Colubridae: Dipsadinae Atractus major, Culebras tierreras cafés Atractus collaris, Culebras tierreras de collares Atractus elaps, Falsas corales tierreras Atractus occipitoalbus, Culebras tierreras grises Atractus snethlageae, Culebras tierreras Clelia clelia, Chontas Dipsas catesbyi, Culebras caracoleras de Catesby Dipsas indica, Culebras caracoleras neotropicales Drepanoides anomalus, Culebras hoz Erythrolamprus reginae, Culebras terrestres reales Erythrolamprus typhlus, Culebras terrestres ciegas Erythrolamprus guentheri, Falsas corales de nuca rosa Helicops angulatus, Culebras de agua anguladas Helicops pastazae, Culebras de agua de Pastaza Helicops leopardinus, Culebras de agua leopardo Helicops petersi, Culebras de agua de Peters Hydrops triangularis, Culebras de agua triángulo Hydrops martii, Culebras de agua amazónicas Imantodes lentiferus, Cordoncillos del Amazonas Imantodes cenchoa, Cordoncillos comunes Leptodeira annulata, Serpientes ojos de gato anilladas Oxyrhopus petolarius, Falsas corales amazónicas Oxyrhopus melanogenys, Falsas corales oscuras Oxyrhopus vanidicus, Falsas corales Philodryas argentea, Serpientes liana verdes de banda plateada Philodryas viridissima, Serpientes corredoras verdes comunes Pseudoboa coronata, Serpiente escarlata amazónica Siphlophis cervinus, Serpientes liana comunes Siphlophis compressus, Falsas corales tropicales Xenodon rabdocephalus, Falsas equis Xenodon severus, Falsas equis orientales Xenopholis scalaris, Serpientes de cabeza plana Taeniophallus brevirostris, Culebras sudamericanas Colubridae: Colubrinae Chironius fuscus, Serpientes látigo olivas Chironius exoletus, Serpientes látigo Chironius monticola, Serpientes látigo de montaña Chironius multiventris, Serpientes látigo Chironius scurrulus, Serpientes látigo de Wagler Chironius carinatus, Serpientes látigo negras Dendrophidion dendrophis, Serpientes corredoras aceituna de bosque Drymobius rhombifer, Culebras con rombos Drymoluber dichrous, Serpientes corredoras comunes brillantes Leptophis ahaetulla, Loras falsas gigantes Oxybelis aeneus, Serpientes liana cafés Oxybelis fulgidus, Serpientes liana verdes Rhinobothryum lentiginosum, Falsas corales anilladas amazónicas Spilotes sulphureus, Serpientes silbadoras gigantes Spilotes pullatus, Serpientes tigre comunes Tantilla melanocephala, Culebras de cabeza negra Phrynonax polylepis, Culebras silbadoras amazónicas Elapidae Micrurus narduccii, Coralillas Micrurus langsdori, Corales de Langsdor Micrurus ornatissimus, Corales ornamentadas Micrurus spixii, Corales amazónicas de cuello negro Micrurus surinamensis, Corales acuáticas Micrurus lemniscatus, Corales acintadas amazónicas Viperidae Bothriopsis bilineata, Oritos machacuy Bothriopsis taeniata, Chichis Bothrocophias hyoprora, Hocicos de puerco Bothrops brazili, Equis de Brasil Bothrops atrox, Equis del oriente Lachesis muta, Verrugosas del oriente Typhlopidae Amerotyphlops reticulatus, Serpientes ciegas gigantes Crocodylia Alligatoridae Caiman crocodilus, Caimanes de anteojos Paleosuchus trigonatus, Caimanes de frente lisa Melanosuchus niger, Caimanes negros Squamata: Sauria Sphaerodactylidae Gonatodes humeralis, Salamanquesas de Trinidad Gonatodes concinnatus, Salamanquesas de tronco Lepidoblepharis festae, Salamanquesas pestañudas orientales Pseudogonatodes guianensis, Salamanquesas Phyllodactylidae Thecadactylus solimoensis, Salamanquesas gigantes orientales Gymnophthalmidae Arthrosaura reticulata, Lagartijas de vientre amarillo Bachia trisanale, Culebras falsas Cercosaura oshaughnessyi, Lagartijas rayadas de O'Shaughnessy Cercosaura argula, Lagartijas rayadas brillantes Cercosaura manicata, Lagartijas rayadas de mangas Iphisa elegans, Lagartijas Potamites ecpleopus, Lagartijas ribereñas Loxopholis parietalis, Lagartijas comunes de las raíces Alopoglossidae Alopoglossus angulatus, Lagartijas Alopoglossus atriventris, Lagartijas de vientre quillado Alopoglossus copii, Lagartijas Ptychoglossus brevifrontalis, Lagartijas Iguanidae: Hoplocercinae Enyalioides cofanorum, Lagartijas de palo cofanes Enyalioides laticeps, Lagartijas de palo cabezonas Iguanidae: Dactyloinae Anolis scypheus, Anolis de escamas doradas Anolis fuscoauratus, Anolis esbeltos Anolis ortonii, Anolis de Orton Anolis punctatus, Anolis manchados Anolis trachyderma, Anolis de piel áspera Anolis transversalis, Anolis de bandas transversales Scincidae Mabuya nigropunctata, Mabuyas de puntos negros Teiidae Kentropyx pelviceps, Lagartijas del bosque Tupinambis cuzcoensis, Tegúes de la selva Iguanidae: Tropidurinae Plica umbra, Lagartijas de labios azules Plica plica, Lagartijas zanqueras de los árboles Uracentron flaviceps, Lagartijas tropicales de cola espinosa Testudines Chelidae Chelus fimbriatus, Tortugas Mata-mata Phrynops georoanus, Tortugas cabeza de sapo de Georoy Platemys platycephala, Charapitas de aguajal Mesoclemmys gibba, Tortugas de Gibba Mesoclemmys heliostemma, Tortugas cabeza de sapo Mesoclemmys raniceps, Tortugas cabeza de sapo de líneas negras Kinosternidae Kinosternon scorpioides, Tortugas tapa-rabo de la Amazonía Podocnemididae Podocnemis expansa, Charapas grandes Podocnemis unifilis, Charapas pequeñas Peltocephalus dumerilianus, Tortugas cabezonas de la Amazonía Testudinidae Chelonoidis denticulatus, Motelos Amphisbaenia Amphisbaenidae Amphisbaena bassleri Culebras ciegas Vanzolini (2002) Orden: Amphisbaenia | Familia: Amphisbaenidae Nombres comunes Pudridoras , Mottled amphisbaenas , Speckled worm lizards , Worm lizards , Culebras ciegas Tamaño El tamaño varía de 300 a 362 mm de longitud (Duellman, 1978; Vitt y de la Torre, 1996). Color en vida Cuerpo blanco a blanco amarillento, raramente blanco rosáceo; marcas dorsales oscuras (negruzcas o azuladas), delgadas y transversales que terminan en los flancos; vientre blanco a blanco amarillento, raramente blanco rosáceo (Duellman, 1978; Vitt y de la Torre, 1996; Vanzolini, 2002). Historia natural Esta especie de hábitos fosoriales es diurna y crepuscular (Vitt y de la Torre, 1996). Poco se conoce sobre su ecología, pero podría ser un forrajeador activo de desplazamiento lento que se alimenta de invertebrados, como hormigas (Formicidae), termitas (Isoptera) y ciempiés (Chilopoda) (Duellman, 1978; Vitt y de la Torre, 1996). Es probablemente ovípara, como la mayoría de anfisbénidos (Duellman, 1978; Vitt y de La Torre, 1996). Andrade et al. (2006) sugieren que los huevos de las especies amazónicas pueden ser colocados en nidos de hormigas y termitas, lo que brindaría rangos de temperatura y humedad favorables para el desarrollo de los embriones, además de servir como mecanismo de defensa ante depredadores o ataques microbianos. Cuando se siente amenazada levanta la cola y la cabeza del suelo, y mueve la cola como si fuese la cabeza. La cola puede autotomizarse una vez (desprenderse), si es atrapada se defiende mordiendo, y aunque no es venenosa sus mordeduras son dolorosas (Vitt y de la Torre, 1996). Distribución y Hábitat Amphisbaena bassleri se distribuye en Bolivia, Perú, norte de Argentina y la Amazonía alta de Ecuador (Gans, 2005). En Ecuador habita entre los 0 a 152 m de altitud, y se la ha reportado en las provincias de Napo, Orellana, Pastaza, Sucumbíos y Morona Santiago (Vanzolini, 2002; Lemos y Facure, 2007). Este reptil habita en bosques de galería, bosques semideciduos y formaciones abiertas, en la hojarasca o bajo tierra. Después de las lluvias se la puede observar sobre el suelo (Vitt y de la Torre, 1996). Regiones naturales Bosque Montano Oriental, Bosque Piemontano Oriental, Bosque Húmedo Tropical Amazónico Pisos Altitudinales Tropical oriental Sistemática Vanzolini (1951, 2002) reconoce cinco subespecies de Amphisbaena fuliginosa, por su coloración y números de escamas. Sin embargo, Gans (2005) propone el cambio de estatus de la subespecie (Amphisbaena fuliginosa bassleri) a especie (Amphisbaena bassleri). Estado de conservación Lista Roja IUCN: No evaluada. Lista Roja Carrillo: Preocupación menor. La destrucción, fragmentación y contaminación del hábitat son sus mayores amenazas. Fomentar los estudios acerca del estado de sus poblaciones naturales sería el primer paso para su conservación. Literatura Citada 1. American Heritage Dictionary. 2006. The American heritage dictionary of the English language. Houghton Milin Harcourt Publishing Company, 2074 pp. 2. Andrade, D. V., Nascimento, L. B. y Abe, A. S. 2006. Habits hidden underground: A review on the reproduction of the Amphisbaenia with notes on four neotropical species. Amphibia-Reptilia 27:207-217. 3. Carrillo, E., Aldás, S., Altamirano-Benavides, M. A., Ayala-Varela, F., Cisneros-Heredia, D. F., Endara, A., Márquez, C., Morales, M., Nogales-Sornosa, F., Salvador, P., Torres, M. L., Valencia, J., Villamarín-Jurado, F., Yánez-Muñoz, M. H. y Zárate, P. 2005. Lista roja de los reptiles del Ecuador. Fundación Novum Milenium, UICN-Sur, UICN-Comité Ecuatoriano, Ministerio de Educación y Cultura, Serie Proyecto Peepe, Quito, Ecuador, 46 pp. 4. CITES. 2017. Apéndices I, II y III. https://cites.org/esp/app/appendices.php (Consultado: 2017). 5. Duellman, W. E. 1978. The biology of an equatorial herpetofauna in Amazonian Ecuador. Miscellaneous Publications of the University of Kansas 65:1-352.
Recommended publications
  • Phylogenetic Diversity, Habitat Loss and Conservation in South
    Diversity and Distributions, (Diversity Distrib.) (2014) 20, 1108–1119 BIODIVERSITY Phylogenetic diversity, habitat loss and RESEARCH conservation in South American pitvipers (Crotalinae: Bothrops and Bothrocophias) Jessica Fenker1, Leonardo G. Tedeschi1, Robert Alexander Pyron2 and Cristiano de C. Nogueira1*,† 1Departamento de Zoologia, Universidade de ABSTRACT Brasılia, 70910-9004 Brasılia, Distrito Aim To analyze impacts of habitat loss on evolutionary diversity and to test Federal, Brazil, 2Department of Biological widely used biodiversity metrics as surrogates for phylogenetic diversity, we Sciences, The George Washington University, 2023 G. St. NW, Washington, DC 20052, study spatial and taxonomic patterns of phylogenetic diversity in a wide-rang- USA ing endemic Neotropical snake lineage. Location South America and the Antilles. Methods We updated distribution maps for 41 taxa, using species distribution A Journal of Conservation Biogeography models and a revised presence-records database. We estimated evolutionary dis- tinctiveness (ED) for each taxon using recent molecular and morphological phylogenies and weighted these values with two measures of extinction risk: percentages of habitat loss and IUCN threat status. We mapped phylogenetic diversity and richness levels and compared phylogenetic distances in pitviper subsets selected via endemism, richness, threat, habitat loss, biome type and the presence in biodiversity hotspots to values obtained in randomized assemblages. Results Evolutionary distinctiveness differed according to the phylogeny used, and conservation assessment ranks varied according to the chosen proxy of extinction risk. Two of the three main areas of high phylogenetic diversity were coincident with areas of high species richness. A third area was identified only by one phylogeny and was not a richness hotspot. Faunal assemblages identified by level of endemism, habitat loss, biome type or the presence in biodiversity hotspots captured phylogenetic diversity levels no better than random assem- blages.
    [Show full text]
  • Checklist of Helminths from Lizards and Amphisbaenians (Reptilia, Squamata) of South America Ticle R A
    The Journal of Venomous Animals and Toxins including Tropical Diseases ISSN 1678-9199 | 2010 | volume 16 | issue 4 | pages 543-572 Checklist of helminths from lizards and amphisbaenians (Reptilia, Squamata) of South America TICLE R A Ávila RW (1), Silva RJ (1) EVIEW R (1) Department of Parasitology, Botucatu Biosciences Institute, São Paulo State University (UNESP – Univ Estadual Paulista), Botucatu, São Paulo State, Brazil. Abstract: A comprehensive and up to date summary of the literature on the helminth parasites of lizards and amphisbaenians from South America is herein presented. One-hundred eighteen lizard species from twelve countries were reported in the literature harboring a total of 155 helminth species, being none acanthocephalans, 15 cestodes, 20 trematodes and 111 nematodes. Of these, one record was from Chile and French Guiana, three from Colombia, three from Uruguay, eight from Bolivia, nine from Surinam, 13 from Paraguay, 12 from Venezuela, 27 from Ecuador, 17 from Argentina, 39 from Peru and 103 from Brazil. The present list provides host, geographical distribution (with the respective biome, when possible), site of infection and references from the parasites. A systematic parasite-host list is also provided. Key words: Cestoda, Nematoda, Trematoda, Squamata, neotropical. INTRODUCTION The present checklist summarizes the diversity of helminths from lizards and amphisbaenians Parasitological studies on helminths that of South America, providing a host-parasite list infect squamates (particularly lizards) in South with localities and biomes. America had recent increased in the past few years, with many new records of hosts and/or STUDIED REGIONS localities and description of several new species (1-3).
    [Show full text]
  • Iii Pontificia Universidad Católica Del
    III PONTIFICIA UNIVERSIDAD CATÓLICA DEL ECUADOR FACULTAD DE CIENCIAS EXACTAS Y NATURALES ESCUELA DE CIENCIAS BIOLÓGICAS Un método integrativo para evaluar el estado de conservación de las especies y su aplicación a los reptiles del Ecuador Tesis previa a la obtención del título de Magister en Biología de la Conservación CAROLINA DEL PILAR REYES PUIG Quito, 2015 IV CERTIFICACIÓN Certifico que la disertación de la Maestría en Biología de la Conservación de la candidata Carolina del Pilar Reyes Puig ha sido concluida de conformidad con las normas establecidas; por tanto, puede ser presentada para la calificación correspondiente. Dr. Omar Torres Carvajal Director de la Disertación Quito, Octubre del 2015 V AGRADECIMIENTOS A Omar Torres-Carvajal, curador de la División de Reptiles del Museo de Zoología de la Pontificia Universidad Católica del Ecuador (QCAZ), por su continua ayuda y contribución en todas las etapas de este estudio. A Andrés Merino-Viteri (QCAZ) por su valiosa ayuda en la generación de mapas de distribución potencial de reptiles del Ecuador. A Santiago Espinosa y Santiago Ron (QCAZ) por sus acertados comentarios y correcciones. A Ana Almendáriz por haber facilitado las localidades geográficas de presencia de ciertos reptiles del Ecuador de la base de datos de la Escuela Politécnica Nacional (EPN). A Mario Yánez-Muñoz de la División de Herpetología del Museo Ecuatoriano de Ciencias Naturales del Instituto Nacional de Biodiversidad (DHMECN-INB), por su ayuda y comentarios a la evaluación de ciertos reptiles del Ecuador. A Marcio Martins, Uri Roll, Fred Kraus, Shai Meiri, Peter Uetz y Omar Torres- Carvajal del Global Assessment of Reptile Distributions (GARD) por su colaboración y comentarios en las encuestas realizadas a expertos.
    [Show full text]
  • Activity Budget and Spatial Behavior of the Emerald Tree Boa Corallus Batesii
    Activity Budget and Spatial Behavior of the Emerald Tree Boa Corallus batesii Faculty Member #1 Joseph R. Mendelson III Signature Faculty Member #2 Emily G. Weigel Signature 2 Acknowledgments I would first like to thank my primary research advisor, Professor Joseph Mendelson, for your guidance and support. Thank you for inviting me to be a part of the emerald boa project and for investing so much time in helping me to become a scientist. I would also like to thank my second research advisor, Professor Emily Weigel, for helping me to get involved in research. Thank you for all of your help with my statistics and analysis and for providing detailed feedback to help me improve my scientific writing. Next, I would like to thank members of my research team: Liz Haseltine, Sav Berry, and Ellen Sproule. Thank you for organizing this study and for your help analyzing our 1,104 hours of video footage. I would like to thank members of the Spatial Ecology and Paleontology lab for your help in training me to become a better researcher. Thank you to Professor Jenny McGuire, Dr. Sílvia Pineda-Munoz, Dr. Yue Wang, Dr. Rachel Short, and Julia Schap. A special thanks to Ben Shipley and Danny Lauer for teaching me how to use R. Finally, I would like to thank my family for your continuous support while I study to become a wildlife biologist. Thank you for listening to me talk about snakes for the past few years. 3 Abstract Corallus batesii is a boid snake native to the Amazon basin.
    [Show full text]
  • On the Geographical Differentiation of Gymnodactylus Geckoides Spix, 1825 (Sauria, Gekkonidae): Speciation in the Brasilian Caatingas
    Anais da Academia Brasileira de Ciências (2004) 76(4): 663-698 (Annals of the Brazilian Academy of Sciences) ISSN 0001-3765 www.scielo.br/aabc On the geographical differentiation of Gymnodactylus geckoides Spix, 1825 (Sauria, Gekkonidae): speciation in the Brasilian caatingas PAULO EMILIO VANZOLINI* Museu de Zoologia da Universidade de São Paulo, Cx. Postal 42694, 04299-970 São Paulo, SP, Brasil Manuscript received on October 31, 2003; accepted for publication on April 4, 2004. ABSTRACT The specific concept of G. geckoides was initially ascertained based on a topotypical sample from Salvador, Bahia. Geographic differentiation was studied through the analysis of two meristic characters (tubercles in a paramedian row and fourth toe lamellae) and color pattern of 327 specimens from 23 localities. It is shown that the population from the southernmost locality, Mucugê, is markedly divergent in all characters studied. A Holocene refuge model is proposed to explain the pattern. A decision about the rank to be attributed to the Mucugê population is deferred until more detailed sampling is effected and molecular methods are applied. Key words: speciation, Holocene refuges, lizards: ecology, lizards: systematics. INTRODUCTION Both the description and the figure are very good. The Gymnodactylus geckoides complex has one of The type locality, environs of the city of Bahia (the the most interesting distributions of all cis-Andean present Salvador), is satisfactorily explicit, and the lizards. It occurs in such diversified areas as the animal is still fairly common there. semi-arid caatingas of northeastern Brazil, the Cen- Fitzinger (1826: 48), in a rather confused note tral Brazilian cerrados, which are mesic open forma- on gekkonid systematics, placed geckoides in his tions, and the humid Atlantic coast.
    [Show full text]
  • Squamata: Sphaerodactylidae) from Northern Venezuela
    Zootaxa 3518: 66–78 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA Copyright © 2012 · Magnolia Press Article ISSN 1175-5334 (online edition) urn:lsid:zoobank.org:pub:83AAFC2D-7895-41F0-B25D-30C591A3FB99 A strikingly polychromatic new species of Gonatodes (Squamata: Sphaerodactylidae) from northern Venezuela CARLOS RIVERO-BLANCO1 & WALTER E. SCHARGEL2* 1Ave. Páez, Resid. General Páez, Edif. B-33, El Paraíso, Caracas 1020, Venezuela. E-mail: [email protected] 2Department of Biology, The University of Texas at Arlington, Arlington, TX 76019, USA. E-mail: [email protected]. *corresponding author Abstract We describe a new species of diurnal gecko, Gonatodes rozei sp. nov., from tropical and premontane humid forests of north central Venezuela. The new species can be distinguished from other congeners by a combination of large size, sub- caudal pattern B (1’1’1’’), three or four lateral scale rows on the digits, males with blue iris, scalation of the gular area, and aspects of color pattern in males and females. The new species is strongly sexually dichromatic and up to four different color morphs are observed in males. Keywords: gecko, lizard, reptile, taxonomy, polymorphic . Introduction The neotropical genus Gonatodes represents a group of mostly diurnal geckos that currently contains 28 species (Rojas-Runjaic et al. 2010; Schargel et al. 2010; Sturaro & Avila-Pires 2011; Kok 2011) collectively distributed from southern Mexico in the north, to Bolivia and Brazil in the south, and including also many islands of the Antilles (Rivero-Blanco 1979). The phylogenetic relationships of members of this genus have been examined recently and its monophyly seems well corroborated (Gamble et al.
    [Show full text]
  • The Reptile Collection of the Museu De Zoologia, Pecies
    Check List 9(2): 257–262, 2013 © 2013 Check List and Authors Chec List ISSN 1809-127X (available at www.checklist.org.br) Journal of species lists and distribution The Reptile Collection of the Museu de Zoologia, PECIES S Universidade Federal da Bahia, Brazil OF Breno Hamdan 1,2*, Daniela Pinto Coelho 1 1, Eduardo José dos Reis Dias3 ISTS 1 L and Rejâne Maria Lira-da-Silva , Annelise Batista D’Angiolella 40170-115, Salvador, BA, Brazil. 1 Universidade Federal da Bahia, Instituto de Biologia, Departamento de Zoologia, Núcleo Regional de Ofiologia e Animais Peçonhentos. CEP Sala A0-92 (subsolo), Laboratório de Répteis, Ilha do Fundão, Av. Carlos Chagas Filho, N° 373. CEP 21941-902. Rio de Janeiro, RJ, Brazil. 2 Programa de Pós-Graduação em Zoologia, Museu Nacional/UFRJ. Universidade Federal do Rio de Janeiro Centro de Ciências da Saúde, Bloco A, Carvalho. CEP 49500-000. Itabaian, SE, Brazil. * 3 CorrUniversidadeesponding Federal author. de E-mail: Sergipe, [email protected] Departamento de Biociências, Laboratório de Biologia e Ecologia de Vertebrados (LABEV), Campus Alberto de Abstract: to its history. The Reptile Collection of the Museu de Zoologia from Universidade Federal da Bahia (CRMZUFBA) has 5,206 specimens and Brazilian 185 species scientific (13 collections endemic to represent Brazil and an 9important threatened) sample with of one the quarter country’s of biodiversitythe known reptile and are species a testament listed in Brazil, from over 175 municipalities. Although the CRMZUFBA houses species from all Brazilian biomes there is a strong regional presence. Knowledge of the species housed in smaller collections could avoid unrepresentative species descriptions and provide information concerning intraspecific variation, ecological features and geographic coverage.
    [Show full text]
  • Boidae, Boinae): a Rare Snake from the Vale Do Ribeira, State of São Paulo, Brazil
    SALAMANDRA 47(2) 112–115 20 May 2011 ISSNCorrespondence 0036–3375 Correspondence New record of Corallus cropanii (Boidae, Boinae): a rare snake from the Vale do Ribeira, State of São Paulo, Brazil Paulo R. Machado-Filho 1, Marcelo R. Duarte 1, Leandro F. do Carmo 2 & Francisco L. Franco 1 1) Laboratório de Herpetologia, Instituto Butantan, Av. Vital Brazil, 1500, São Paulo, SP, CEP: 05503-900, Brazil 2) Departamento de Agroindústria, Alimentos e Nutrição. Escola Superior de Agronomia “Luiz de Queiroz” – ESALQ/USP, Av. Pádua Dias, 11 C.P.: 9, Piracicaba, SP, CEP: 13418-900, Brazil Correspondig author: Francisco L. Franco, e-mail: [email protected] Manuscript received: 9 December 2010 The boid genusCorallus Daudin, 1803 is comprised of nine Until recently, only four specimens (including the above Neotropical species (Henderson et al. 2009): Corallus an­ mentioned holotype) of C. cropanii were deposited in her- nulatus (Cope, 1876), Corallus batesii (Gray, 1860), Co­ petological collections: three in the Coleção Herpetológica rallus blombergi (Rendahl & Vestergren, 1941), Coral­ “Alphonse Richard Hoge”, Instituto Butantan, São Paulo, lus caninus (Linnaeus, 1758), Corallus cookii Gray, 1842, Corallus cropanii (Hoge, 1954), Corallus grenadensis (Bar- bour, 1914), Corallus hortulanus (Linnaeus, 1758), and Corallus ruschenbergerii (Cope, 1876). The most conspic- uous morphological attributes of representatives of these species are the laterally compressed body, robust head, slim neck, and the presence of deep pits in some of the la- bial scales (Henderson 1993a, 1997). Species of Corallus are distributed from northern Central American to south- ern Brazil, including Trinidad and Tobago and islands of the south Caribbean. Four species occur in Brazil: Corallus batesii, C.
    [Show full text]
  • Check List 8(2): 207-210, 2012 © 2012 Check List and Authors Chec List ISSN 1809-127X (Available at Journal of Species Lists and Distribution
    Check List 8(2): 207-210, 2012 © 2012 Check List and Authors Chec List ISSN 1809-127X (available at www.checklist.org.br) Journal of species lists and distribution Amphibians and Reptiles from Paramakatoi and Kato, PECIES S Guyana OF ISTS 1* 2 L Ross D. MacCulloch and Robert P. Reynolds 1 Royal Ontario Museum, Department of Natural History. 100 Queen’s Park, Toronto, Ontario M5S 2C6, Canada. 2 National Museum of Natural History, USGS Patuxent Wildlife Research Center, MRC 111, P.O. Box 37012, Washington, D.C. 20013-7012, USA. * Corresponding author. E-mail: [email protected] Abstract: We report the herpetofauna of two neighboring upland locations in west-central Guyana. Twenty amphibian and 24 reptile species were collected. Only 40% of amphibians and 12.5% of reptiles were collected in both locations. This is one of the few collections made at upland (750–800 m) locations in the Guiana Shield. Introduction palm stands (Maurita flexuosa) (Hollowell et al. 2003). The Guiana Shield region of northeastern South America Immediately west of Kato is the nearby Chiung River, is one of the world’s areas of greatest biodiversity. The a rocky-bottomed watercourse about 50 m wide with herpetofauna of the region remains poorly documented, numerous small falls and a distinct riparian zone. Many although there have been several general publications small agricultural clearings, in typical rotating “slash and on the subject (Starace 1998; Gorzula and Señaris 1999; burn” fashion, are common around Kato in the areas where Lescure and Marty 2000; Reynolds et al. 2001; Avila- savanna transitions to forest.
    [Show full text]
  • Ecological Functions of Neotropical Amphibians and Reptiles: a Review
    Univ. Sci. 2015, Vol. 20 (2): 229-245 doi: 10.11144/Javeriana.SC20-2.efna Freely available on line REVIEW ARTICLE Ecological functions of neotropical amphibians and reptiles: a review Cortés-Gomez AM1, Ruiz-Agudelo CA2 , Valencia-Aguilar A3, Ladle RJ4 Abstract Amphibians and reptiles (herps) are the most abundant and diverse vertebrate taxa in tropical ecosystems. Nevertheless, little is known about their role in maintaining and regulating ecosystem functions and, by extension, their potential value for supporting ecosystem services. Here, we review research on the ecological functions of Neotropical herps, in different sources (the bibliographic databases, book chapters, etc.). A total of 167 Neotropical herpetology studies published over the last four decades (1970 to 2014) were reviewed, providing information on more than 100 species that contribute to at least five categories of ecological functions: i) nutrient cycling; ii) bioturbation; iii) pollination; iv) seed dispersal, and; v) energy flow through ecosystems. We emphasize the need to expand the knowledge about ecological functions in Neotropical ecosystems and the mechanisms behind these, through the study of functional traits and analysis of ecological processes. Many of these functions provide key ecosystem services, such as biological pest control, seed dispersal and water quality. By knowing and understanding the functions that perform the herps in ecosystems, management plans for cultural landscapes, restoration or recovery projects of landscapes that involve aquatic and terrestrial systems, development of comprehensive plans and detailed conservation of species and ecosystems may be structured in a more appropriate way. Besides information gaps identified in this review, this contribution explores these issues in terms of better understanding of key questions in the study of ecosystem services and biodiversity and, also, of how these services are generated.
    [Show full text]
  • <I>Alopoglossus Atriventris
    HERPETOLOGICAL JOURNAL 17: 269–272, 2007 digenean Mesocoelium monas in Prionodactylus Short Note eigenmanni, also from Brazil. The purpose of this paper is to present an initial helminth list for Alopoglossus angulatus and A. atriventris. Parasite communities of two Nineteen Alopoglossus angulatus (mean snout–vent length [SVL] = 42.1±13.4 mm, range 24–60 mm) and 16 A. lizard species, Alopoglossus atriventris (SVL = 36.9±9.2 mm, range 21–48 mm) were angulatus and Alopoglossus borrowed from the herpetology collection of the Sam No- ble Oklahoma Museum of Natural History (OMNH) and atriventris, from Brazil and examined for helminths. Stomachs from these lizards had previously been removed and were not available for this Ecuador study. Collection localities are as follows. Alopoglossus angulatus: 14 (OMNH 36931–36944) from Acre state, Bra- Stephen R. Goldberg1, Charles R. zil 1996; one (OMNH 37125) from Amazonas state, Brazil Bursey2 & Laurie J. Vitt3 1997; one (OMNH 37337) from Rondônia state, Brazil 1998; three (OMNH 36440–36442) from Sucumbíos prov- 1Department of Biology, Whittier College, California, USA ince, Ecuador 1994. Alopoglossus atriventris: eight 2Department of Biology, Pennsylvania State University, USA (OMNH 36945–36952) from Acre state, Brazil 1996; four 3Sam Noble Oklahoma Museum of Natural History and (OMNH 37126–37129) from Amazonas state, Brazil 1997; Zoology Department, University of Oklahoma, USA two (OMNH 37637–37638) from Amazonas state, Brazil 1998; two (OMNH 36438–36439) from Sucumbíos prov- Alopoglossus angulatus and A. atriventris from Brazil ince, Ecuador 1994. These lizards had originally been fixed and Ecuador were examined for endoparasites. in 10% formalin and stored in 70% ethanol.
    [Show full text]
  • Distribution and Natural History of the Ecuadorian Toad-Headed Pitvipers of the Genus Bothrocophias (Squamata: Serpentes: Viperidae: Crotalinae)
    ©Österreichische Gesellschaft für Herpetologie e.V., Wien, Austria, download unter www.biologiezentrum.at HERPETOZOA 19 (1/2): 17-26 17 Wien, 30. Juli 2006 Distribution and natural history of the Ecuadorian Toad-headed Pitvipers of the genus Bothrocophias (Squamata: Serpentes: Viperidae: Crotalinae) Verbreitung und Naturgeschichte der ecuadorianischen Krötenkopf-Grubenottern der Gattung Bothrocophias (Squamata: Serpentes: Viperidae: Crotalinae) DIEGO F. CISNEROS-HEREDIA & MARIA OLGA BORJA & DANIEL PROANO & JEAN-MARC TOUZET KURZFASSUNG Spärlich sind die Kenntnisse über Grubenottern der Gattung Bothrocophias. Die vorliegende Arbeit enthält Informationen zu drei Bothrocophias Arten aus Ecuador: Bothrocophias campbelli (FREIRE LASCANO, 1991), B. hyoprora (AMARAL, 1935) und B. microphthalmus (COPE, 1875), einschließlich Angaben zur geographischen und vertikalen Verbreitung, zu Nachweisen in den Provinzen, sympatrischen Grubenotternarten, Aktivitätsmustern, Verhalten, Körpergröße, Fortpflanzungsbiologie, Nahrung und Lebensalter. Bothrocophias campbelli bewohnt die nördlichen, zentralen und südlichen Gebiete der pazifischen Andenabhänge Ecuadors zwischen 800 und 2000 m; Bothrocophias hyoprora kommt im nördlichen und südlichen Amazonastiefland und an den unteren östlichen Hän- gen der Anden Ecuadors zwischen 210 und 1500 m vor, Bothrocophias microphthalmus an deren Südosthängen zwischen 600 und 2350 m. Die Arbeit berichtet über den zweiten Fundortnachweis von B. campbelli in der Provinz Imbabura und den westlichsten Fundort von B. hyoprora im Tal des Nangaritza Flusses. Das ympatrische Vorkom- men von B. hyoprora und B. microphthalmus im Makuma-Gebiet, Provinz Morona-Santiago, wird bestätigt, was die bisher bekannte obere Verbreitungsgrenze von B. microphthalmus auf zumindest 600 m anhebt. Das Weiß- bauch-Mausopossum Marmosops noctivagus wird erstmals als Beutetier von B. microphthalmus beschrieben. Die neuen Daten über die Fortpflanzungsbiologie von Grubenottern der Gattung Bothrocophias umfassen Wurfgröße und Körperlänge Neugeborener bei B.
    [Show full text]