Conservation Actions for Native and Threatened Amphibians of Colombian Caribbean Region
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A Collection of Amphibians from Río San Juan, Southeastern Nicaragua
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/264789493 A collection of amphibians from Río San Juan, southeastern Nicaragua Article in Herpetology Notes · January 2009 CITATIONS READS 12 188 4 authors, including: Javier Sunyer Matthias Dehling University of Canterbury 89 PUBLICATIONS 209 CITATIONS 54 PUBLICATIONS 967 CITATIONS SEE PROFILE SEE PROFILE Gunther Köhler Senckenberg Research Institute 222 PUBLICATIONS 1,617 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Zoological Research in Strict Forest Reserves in Hesse, Germany View project Diploma Thesis View project All content following this page was uploaded by Javier Sunyer on 16 August 2018. The user has requested enhancement of the downloaded file. Herpetology Notes, volume 2: 189-202 (2009) (published online on 29 October 2009) A collection of amphibians from Río San Juan, southeastern Nicaragua Javier Sunyer1,2,3*, Guillermo Páiz4, David Matthias Dehling1, Gunther Köhler1 Abstract. We report upon the amphibians collected during seven expeditions carried out between the years 2000–2006 to thirteen localities in both Refugio de Vida Silvestre Río San Juan and Reserva Biológica Indio-Maíz, southeastern Nicaragua. We include morphometric data of around one-half of the adult specimens in the collection, and provide a brief general overview and discuss zoogeographic and conservation considerations of the amphibians known to occur in the Río San Juan area. Keywords. Amphibia, conservation, ecology, morphometry, zoogeography. Introduction potential of holding America’s first interoceanic channel and also because it was part of the sea route to travel The San Juan River is an approximately 200 km slow- from eastern to western United States. -
Catalogue of the Amphibians of Venezuela: Illustrated and Annotated Species List, Distribution, and Conservation 1,2César L
Mannophryne vulcano, Male carrying tadpoles. El Ávila (Parque Nacional Guairarepano), Distrito Federal. Photo: Jose Vieira. We want to dedicate this work to some outstanding individuals who encouraged us, directly or indirectly, and are no longer with us. They were colleagues and close friends, and their friendship will remain for years to come. César Molina Rodríguez (1960–2015) Erik Arrieta Márquez (1978–2008) Jose Ayarzagüena Sanz (1952–2011) Saúl Gutiérrez Eljuri (1960–2012) Juan Rivero (1923–2014) Luis Scott (1948–2011) Marco Natera Mumaw (1972–2010) Official journal website: Amphibian & Reptile Conservation amphibian-reptile-conservation.org 13(1) [Special Section]: 1–198 (e180). Catalogue of the amphibians of Venezuela: Illustrated and annotated species list, distribution, and conservation 1,2César L. Barrio-Amorós, 3,4Fernando J. M. Rojas-Runjaic, and 5J. Celsa Señaris 1Fundación AndígenA, Apartado Postal 210, Mérida, VENEZUELA 2Current address: Doc Frog Expeditions, Uvita de Osa, COSTA RICA 3Fundación La Salle de Ciencias Naturales, Museo de Historia Natural La Salle, Apartado Postal 1930, Caracas 1010-A, VENEZUELA 4Current address: Pontifícia Universidade Católica do Río Grande do Sul (PUCRS), Laboratório de Sistemática de Vertebrados, Av. Ipiranga 6681, Porto Alegre, RS 90619–900, BRAZIL 5Instituto Venezolano de Investigaciones Científicas, Altos de Pipe, apartado 20632, Caracas 1020, VENEZUELA Abstract.—Presented is an annotated checklist of the amphibians of Venezuela, current as of December 2018. The last comprehensive list (Barrio-Amorós 2009c) included a total of 333 species, while the current catalogue lists 387 species (370 anurans, 10 caecilians, and seven salamanders), including 28 species not yet described or properly identified. Fifty species and four genera are added to the previous list, 25 species are deleted, and 47 experienced nomenclatural changes. -
For Review Only
Page 63 of 123 Evolution Moen et al. 1 1 2 3 4 5 Appendix S1: Supplementary data 6 7 Table S1 . Estimates of local species composition at 39 sites in Middle America based on data summarized by Duellman 8 9 10 (2001). Locality numbers correspond to Table 2. References for body size and larval habitat data are found in Table S2. 11 12 Locality and elevation Body Larval Subclade within Middle Species present Hylid clade 13 (country, state, specific location)For Reviewsize Only habitat American clade 14 15 16 1) Mexico, Sonora, Alamos; 597 m Pachymedusa dacnicolor 82.6 pond Phyllomedusinae 17 Smilisca baudinii 76.0 pond Middle American Smilisca clade 18 Smilisca fodiens 62.6 pond Middle American Smilisca clade 19 20 21 2) Mexico, Sinaloa, Mazatlan; 9 m Pachymedusa dacnicolor 82.6 pond Phyllomedusinae 22 Smilisca baudinii 76.0 pond Middle American Smilisca clade 23 Smilisca fodiens 62.6 pond Middle American Smilisca clade 24 Tlalocohyla smithii 26.0 pond Middle American Tlalocohyla 25 Diaglena spatulata 85.9 pond Middle American Smilisca clade 26 27 28 3) Mexico, Durango, El Salto; 2603 Hyla eximia 35.0 pond Middle American Hyla 29 m 30 31 32 4) Mexico, Jalisco, Chamela; 11 m Dendropsophus sartori 26.0 pond Dendropsophus 33 Exerodonta smaragdina 26.0 stream Middle American Plectrohyla clade 34 Pachymedusa dacnicolor 82.6 pond Phyllomedusinae 35 Smilisca baudinii 76.0 pond Middle American Smilisca clade 36 Smilisca fodiens 62.6 pond Middle American Smilisca clade 37 38 Tlalocohyla smithii 26.0 pond Middle American Tlalocohyla 39 Diaglena spatulata 85.9 pond Middle American Smilisca clade 40 Trachycephalus venulosus 101.0 pond Lophiohylini 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 Evolution Page 64 of 123 Moen et al. -
Identification of the Taxonomic Status of Scinax Nebulosus and Scinax Constrictus (Scinaxinae, Anura) Based on Molecular Markers T
Brazilian Journal of Biology https://doi.org/10.1590/1519-6984.225646 ISSN 1519-6984 (Print) Original Article ISSN 1678-4375 (Online) Identification of the taxonomic status of Scinax nebulosus and Scinax constrictus (Scinaxinae, Anura) based on molecular markers T. M. B. Freitasa* , J. B. L. Salesb , I. Sampaioc , N. M. Piorskia and L. N. Weberd aUniversidade Federal do Maranhão – UFMA, Departamento de Biologia, Laboratório de Ecologia e Sistemática de Peixes, Programa de Pós-graduação Bionorte, Grupo de Taxonomia, Biogeografia, Ecologia e Conservação de Peixes do Maranhão, São Luís, MA, Brasil bUniversidade Federal do Pará – UFPA, Centro de Estudos Avançados da Biodiversidade – CEABIO, Programa de Pós-graduação em Ecologia Aquática e Pesca – PPGEAP, Grupo de Investigação Biológica Integrada – GIBI, Belém, PA, Brasil cUniversidade Federal do Pará – UFPA, Instituto de Estudos Costeiros – IECOS, Laboratório e Filogenomica e Bioinformatica, Programa de Pós-graduação Biologia Ambiental – PPBA, Grupo de Estudos em Genética e Filogenômica, Bragança, PA, Brasil dUniversidade Federal do Sul da Bahia – UFSB, Centro de Formação em Ciências Ambientais, Instituto Sosígenes Costa de Humanidades, Artes e Ciências, Departamento de Ciências Biológicas, Laboratório de Zoologia, Programa de Pós-graduação Bionorte, Grupo Biodiversidade da Fauna do Sul da Bahia, Porto Seguro, BA, Brasil *e-mail: [email protected] Received: June 26, 2019 – Accepted: May 4, 2020 – Distributed: November 30, 2021 (With 4 figures) Abstract The validation of many anuran species is based on a strictly descriptive, morphological analysis of a small number of specimens with a limited geographic distribution. The Scinax Wagler, 1830 genus is a controversial group with many doubtful taxa and taxonomic uncertainties, due a high number of cryptic species. -
The Most Frog-Diverse Place in Middle America, with Notes on The
Offcial journal website: Amphibian & Reptile Conservation amphibian-reptile-conservation.org 13(2) [Special Section]: 304–322 (e215). The most frog-diverse place in Middle America, with notes on the conservation status of eight threatened species of amphibians 1,2,*José Andrés Salazar-Zúñiga, 1,2,3Wagner Chaves-Acuña, 2Gerardo Chaves, 1Alejandro Acuña, 1,2Juan Ignacio Abarca-Odio, 1,4Javier Lobon-Rovira, 1,2Edwin Gómez-Méndez, 1,2Ana Cecilia Gutiérrez-Vannucchi, and 2Federico Bolaños 1Veragua Foundation for Rainforest Research, Limón, COSTA RICA 2Escuela de Biología, Universidad de Costa Rica, San Pedro, 11501-2060 San José, COSTA RICA 3División Herpetología, Museo Argentino de Ciencias Naturales ‘‘Bernardino Rivadavia’’-CONICET, C1405DJR, Buenos Aires, ARGENTINA 4CIBIO Research Centre in Biodiversity and Genetic Resources, InBIO, Universidade do Porto, Campus Agrário de Vairão, Rua Padre Armando Quintas 7, 4485-661 Vairão, Vila do Conde, PORTUGAL Abstract.—Regarding amphibians, Costa Rica exhibits the greatest species richness per unit area in Middle America, with a total of 215 species reported to date. However, this number is likely an underestimate due to the presence of many unexplored areas that are diffcult to access. Between 2012 and 2017, a monitoring survey of amphibians was conducted in the Central Caribbean of Costa Rica, on the northern edge of the Matama mountains in the Talamanca mountain range, to study the distribution patterns and natural history of species across this region, particularly those considered as endangered by the International Union for Conservation of Nature. The results show the highest amphibian species richness among Middle America lowland evergreen forests, with a notable anuran representation of 64 species. -
Final Report
Final Report Contents Report Credits.........................................................................................................ii Executive Summary.................................................................................................1 Introduction............................................................................................................2 Methods Plant Group................................................................................................3 Bird Group..................................................................................................3 Mammal Group..........................................................................................4 Reptile and Amphibian Group....................................................................4 Marine Group.............................................................................................4 Freshwater Group.......................................................................................5 Terrestrial Invertebrate Group...................................................................6 Fungi...........................................................................................................7 Public Participation.....................................................................................7 Results and Discussion Plant Group.................................................................................................8 Bird Group...................................................................................................8 -
A Review of Chemical Defense in Poison Frogs (Dendrobatidae): Ecology, Pharmacokinetics, and Autoresistance
Chapter 21 A Review of Chemical Defense in Poison Frogs (Dendrobatidae): Ecology, Pharmacokinetics, and Autoresistance Juan C. Santos , Rebecca D. Tarvin , and Lauren A. O’Connell 21.1 Introduction Chemical defense has evolved multiple times in nearly every major group of life, from snakes and insects to bacteria and plants (Mebs 2002 ). However, among land vertebrates, chemical defenses are restricted to a few monophyletic groups (i.e., clades). Most of these are amphibians and snakes, but a few rare origins (e.g., Pitohui birds) have stimulated research on acquired chemical defenses (Dumbacher et al. 1992 ). Selective pressures that lead to defense are usually associated with an organ- ism’s limited ability to escape predation or conspicuous behaviors and phenotypes that increase detectability by predators (e.g., diurnality or mating calls) (Speed and Ruxton 2005 ). Defended organisms frequently evolve warning signals to advertise their defense, a phenomenon known as aposematism (Mappes et al. 2005 ). Warning signals such as conspicuous coloration unambiguously inform predators that there will be a substantial cost if they proceed with attack or consumption of the defended prey (Mappes et al. 2005 ). However, aposematism is likely more complex than the simple pairing of signal and defense, encompassing a series of traits (i.e., the apose- matic syndrome) that alter morphology, physiology, and behavior (Mappes and J. C. Santos (*) Department of Zoology, Biodiversity Research Centre , University of British Columbia , #4200-6270 University Blvd , Vancouver , BC , Canada , V6T 1Z4 e-mail: [email protected] R. D. Tarvin University of Texas at Austin , 2415 Speedway Stop C0990 , Austin , TX 78712 , USA e-mail: [email protected] L. -
Taxonomic Checklist of Amphibian Species Listed in the CITES
CoP17 Doc. 81.1 Annex 5 (English only / Únicamente en inglés / Seulement en anglais) Taxonomic Checklist of Amphibian Species listed in the CITES Appendices and the Annexes of EC Regulation 338/97 Species information extracted from FROST, D. R. (2015) "Amphibian Species of the World, an online Reference" V. 6.0 (as of May 2015) Copyright © 1998-2015, Darrel Frost and TheAmericanMuseum of Natural History. All Rights Reserved. Additional comments included by the Nomenclature Specialist of the CITES Animals Committee (indicated by "NC comment") Reproduction for commercial purposes prohibited. CoP17 Doc. 81.1 Annex 5 - p. 1 Amphibian Species covered by this Checklist listed by listed by CITES EC- as well as Family Species Regulation EC 338/97 Regulation only 338/97 ANURA Aromobatidae Allobates femoralis X Aromobatidae Allobates hodli X Aromobatidae Allobates myersi X Aromobatidae Allobates zaparo X Aromobatidae Anomaloglossus rufulus X Bufonidae Altiphrynoides malcolmi X Bufonidae Altiphrynoides osgoodi X Bufonidae Amietophrynus channingi X Bufonidae Amietophrynus superciliaris X Bufonidae Atelopus zeteki X Bufonidae Incilius periglenes X Bufonidae Nectophrynoides asperginis X Bufonidae Nectophrynoides cryptus X Bufonidae Nectophrynoides frontierei X Bufonidae Nectophrynoides laevis X Bufonidae Nectophrynoides laticeps X Bufonidae Nectophrynoides minutus X Bufonidae Nectophrynoides paulae X Bufonidae Nectophrynoides poyntoni X Bufonidae Nectophrynoides pseudotornieri X Bufonidae Nectophrynoides tornieri X Bufonidae Nectophrynoides vestergaardi -
Herpetology at the Isthmus Species Checklist
Herpetology at the Isthmus Species Checklist AMPHIBIANS BUFONIDAE true toads Atelopus zeteki Panamanian Golden Frog Incilius coniferus Green Climbing Toad Incilius signifer Panama Dry Forest Toad Rhaebo haematiticus Truando Toad (Litter Toad) Rhinella alata South American Common Toad Rhinella granulosa Granular Toad Rhinella margaritifera South American Common Toad Rhinella marina Cane Toad CENTROLENIDAE glass frogs Cochranella euknemos Fringe-limbed Glass Frog Cochranella granulosa Grainy Cochran Frog Espadarana prosoblepon Emerald Glass Frog Sachatamia albomaculata Yellow-flecked Glass Frog Sachatamia ilex Ghost Glass Frog Teratohyla pulverata Chiriqui Glass Frog Teratohyla spinosa Spiny Cochran Frog Hyalinobatrachium chirripoi Suretka Glass Frog Hyalinobatrachium colymbiphyllum Plantation Glass Frog Hyalinobatrachium fleischmanni Fleischmann’s Glass Frog Hyalinobatrachium valeroi Reticulated Glass Frog Hyalinobatrachium vireovittatum Starrett’s Glass Frog CRAUGASTORIDAE robber frogs Craugastor bransfordii Bransford’s Robber Frog Craugastor crassidigitus Isla Bonita Robber Frog Craugastor fitzingeri Fitzinger’s Robber Frog Craugastor gollmeri Evergreen Robber Frog Craugastor megacephalus Veragua Robber Frog Craugastor noblei Noble’s Robber Frog Craugastor stejnegerianus Stejneger’s Robber Frog Craugastor tabasarae Tabasara Robber Frog Craugastor talamancae Almirante Robber Frog DENDROBATIDAE poison dart frogs Allobates talamancae Striped (Talamanca) Rocket Frog Colostethus panamensis Panama Rocket Frog Colostethus pratti Pratt’s Rocket -
BOA5.1-2 Frog Biology, Taxonomy and Biodiversity
The Biology of Amphibians Agnes Scott College Mark Mandica Executive Director The Amphibian Foundation [email protected] 678 379 TOAD (8623) Phyllomedusidae: Agalychnis annae 5.1-2: Frog Biology, Taxonomy & Biodiversity Part 2, Neobatrachia Hylidae: Dendropsophus ebraccatus CLassification of Order: Anura † Triadobatrachus Ascaphidae Leiopelmatidae Bombinatoridae Alytidae (Discoglossidae) Pipidae Rhynophrynidae Scaphiopopidae Pelodytidae Megophryidae Pelobatidae Heleophrynidae Nasikabatrachidae Sooglossidae Calyptocephalellidae Myobatrachidae Alsodidae Batrachylidae Bufonidae Ceratophryidae Cycloramphidae Hemiphractidae Hylodidae Leptodactylidae Odontophrynidae Rhinodermatidae Telmatobiidae Allophrynidae Centrolenidae Hylidae Dendrobatidae Brachycephalidae Ceuthomantidae Craugastoridae Eleutherodactylidae Strabomantidae Arthroleptidae Hyperoliidae Breviceptidae Hemisotidae Microhylidae Ceratobatrachidae Conrauidae Micrixalidae Nyctibatrachidae Petropedetidae Phrynobatrachidae Ptychadenidae Ranidae Ranixalidae Dicroglossidae Pyxicephalidae Rhacophoridae Mantellidae A B † 3 † † † Actinopterygian Coelacanth, Tetrapodomorpha †Amniota *Gerobatrachus (Ray-fin Fishes) Lungfish (stem-tetrapods) (Reptiles, Mammals)Lepospondyls † (’frogomander’) Eocaecilia GymnophionaKaraurus Caudata Triadobatrachus 2 Anura Sub Orders Super Families (including Apoda Urodela Prosalirus †) 1 Archaeobatrachia A Hyloidea 2 Mesobatrachia B Ranoidea 1 Anura Salientia 3 Neobatrachia Batrachia Lissamphibia *Gerobatrachus may be the sister taxon Salientia Temnospondyls -
Phylogenetic Analyses of Rates of Body Size Evolution Should Show
SSStttooonnnyyy BBBrrrooooookkk UUUnnniiivvveeerrrsssiiitttyyy The official electronic file of this thesis or dissertation is maintained by the University Libraries on behalf of The Graduate School at Stony Brook University. ©©© AAAllllll RRRiiiggghhhtttsss RRReeessseeerrrvvveeeddd bbbyyy AAAuuuttthhhooorrr... The origins of diversity in frog communities: phylogeny, morphology, performance, and dispersal A Dissertation Presented by Daniel Steven Moen to The Graduate School in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy in Ecology and Evolution Stony Brook University August 2012 Stony Brook University The Graduate School Daniel Steven Moen We, the dissertation committee for the above candidate for the Doctor of Philosophy degree, hereby recommend acceptance of this dissertation. John J. Wiens – Dissertation Advisor Associate Professor, Ecology and Evolution Douglas J. Futuyma – Chairperson of Defense Distinguished Professor, Ecology and Evolution Stephan B. Munch – Ecology & Evolution Graduate Program Faculty Adjunct Associate Professor, Marine Sciences Research Center Duncan J. Irschick – Outside Committee Member Professor, Biology Department University of Massachusetts at Amherst This dissertation is accepted by the Graduate School Charles Taber Interim Dean of the Graduate School ii Abstract of the Dissertation The origins of diversity in frog communities: phylogeny, morphology, performance, and dispersal by Daniel Steven Moen Doctor of Philosophy in Ecology and Evolution Stony Brook University 2012 In this dissertation, I combine phylogenetics, comparative methods, and studies of morphology and ecological performance to understand the evolutionary and biogeographical factors that lead to the community structure we see today in frogs. In Chapter 1, I first summarize the conceptual background of the entire dissertation. In Chapter 2, I address the historical processes influencing body-size evolution in treefrogs by studying body-size diversification within Caribbean treefrogs (Hylidae: Osteopilus ). -
The Global Amphibian Trade Flows Through Europe: the Need for Enforcing and Improving Legislation
Biodivers Conserv DOI 10.1007/s10531-016-1193-8 REVIEW PAPER The global amphibian trade flows through Europe: the need for enforcing and improving legislation 1 2 3,4 Mark Auliya • Jaime Garcı´a-Moreno • Benedikt R. Schmidt • 1 5 6 Dirk S. Schmeller • Marinus S. Hoogmoed • Matthew C. Fisher • 7 1 8 Frank Pasmans • Klaus Henle • David Bickford • An Martel7 Received: 15 December 2015 / Revised: 11 August 2016 / Accepted: 13 August 2016 Ó Springer Science+Business Media Dordrecht 2016 Abstract The global amphibian trade is suspected to have brought several species to the brink of extinction, and has led to the spread of amphibian pathogens. Moreover, inter- national trade is not regulated for *98 % of species. Here we outline patterns and com- plexity underlying global amphibian trade, highlighting some loopholes that need to be addressed, focusing on the European Union. In spite of being one of the leading amphibian importers, the EU’s current legislation is insufficient to prevent overharvesting of those species in demand or the introduction and/or spread of amphibian pathogens into captive and wild populations. We suggest steps to improve the policy (implementation and enforcement) framework, including (i) an identifier specifically for amphibians in the Communicated by David Hawksworth. This article belongs to the Topical Collection: Biodiversity legal instruments and regulations. & Mark Auliya [email protected] & Jaime Garcı´a-Moreno [email protected] 1 Department of Conservation Biology, UFZ—Helmholtz Centre for Environmental Research,