FROGLOG Edi- to Publish a Synopsis in FROGLOG
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
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. -
Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca
Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca John F. Lamoreux, Meghan W. McKnight, and Rodolfo Cabrera Hernandez Occasional Paper of the IUCN Species Survival Commission No. 53 Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca John F. Lamoreux, Meghan W. McKnight, and Rodolfo Cabrera Hernandez Occasional Paper of the IUCN Species Survival Commission No. 53 The designation of geographical entities in this book, and the presentation of the material, do not imply the expression of any opinion whatsoever on the part of IUCN concerning the legal status of any country, territory, or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. The views expressed in this publication do not necessarily reflect those of IUCN or other participating organizations. Published by: IUCN, Gland, Switzerland Copyright: © 2015 International Union for Conservation of Nature and Natural Resources Reproduction of this publication for educational or other non-commercial purposes is authorized without prior written permission from the copyright holder provided the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited without prior written permission of the copyright holder. Citation: Lamoreux, J. F., McKnight, M. W., and R. Cabrera Hernandez (2015). Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca. Gland, Switzerland: IUCN. xxiv + 320pp. ISBN: 978-2-8317-1717-3 DOI: 10.2305/IUCN.CH.2015.SSC-OP.53.en Cover photographs: Totontepec landscape; new Plectrohyla species, Ixalotriton niger, Concepción Pápalo, Thorius minutissimus, Craugastor pozo (panels, left to right) Back cover photograph: Collecting in Chamula, Chiapas Photo credits: The cover photographs were taken by the authors under grant agreements with the two main project funders: NGS and CEPF. -
Goliath Frogs Build Nests for Spawning – the Reason for Their Gigantism? Marvin Schäfera, Sedrick Junior Tsekanéb, F
JOURNAL OF NATURAL HISTORY 2019, VOL. 53, NOS. 21–22, 1263–1276 https://doi.org/10.1080/00222933.2019.1642528 Goliath frogs build nests for spawning – the reason for their gigantism? Marvin Schäfera, Sedrick Junior Tsekanéb, F. Arnaud M. Tchassemb, Sanja Drakulića,b,c, Marina Kamenib, Nono L. Gonwouob and Mark-Oliver Rödel a,b,c aMuseum für Naturkunde, Leibniz Institute for Evolution and Biodiversity Science, Berlin, Germany; bFaculty of Science, Laboratory of Zoology, University of Yaoundé I, Yaoundé, Cameroon; cFrogs & Friends, Berlin, Germany ABSTRACT ARTICLE HISTORY In contrast to its popularity, astonishingly few facts have become Received 16 April 2019 known about the biology of the Goliath Frog, Conraua goliath.We Accepted 7 July 2019 herein report the so far unknown construction of nests as spawning KEYWORDS sites by this species. On the Mpoula River, Littoral District, West Amphibia; Anura; Cameroon; Cameroon we identified 19 nests along a 400 m section. Nests Conraua goliath; Conrauidae; could be classified into three types. Type 1 constitutes rock pools parental care that were cleared by the frogs from detritus and leaf-litter; type 2 constitutes existing washouts at the riverbanks that were cleared from leaf-litter and/or expanded, and type 3 were depressions dug by the frogs into gravel riverbanks. The cleaning and digging activ- ities of the frogs included removal of small to larger items, ranging from sand and leaves to larger stones. In all nest types eggs and tadpoles of C. goliath were detected. All nest types were used for egg deposition several times, and could comprise up to three distinct cohorts of tadpoles. -
Biodiversity in Sub-Saharan Africa and Its Islands Conservation, Management and Sustainable Use
Biodiversity in Sub-Saharan Africa and its Islands Conservation, Management and Sustainable Use Occasional Papers of the IUCN Species Survival Commission No. 6 IUCN - The World Conservation Union IUCN Species Survival Commission Role of the SSC The Species Survival Commission (SSC) is IUCN's primary source of the 4. To provide advice, information, and expertise to the Secretariat of the scientific and technical information required for the maintenance of biologi- Convention on International Trade in Endangered Species of Wild Fauna cal diversity through the conservation of endangered and vulnerable species and Flora (CITES) and other international agreements affecting conser- of fauna and flora, whilst recommending and promoting measures for their vation of species or biological diversity. conservation, and for the management of other species of conservation con- cern. Its objective is to mobilize action to prevent the extinction of species, 5. To carry out specific tasks on behalf of the Union, including: sub-species and discrete populations of fauna and flora, thereby not only maintaining biological diversity but improving the status of endangered and • coordination of a programme of activities for the conservation of bio- vulnerable species. logical diversity within the framework of the IUCN Conservation Programme. Objectives of the SSC • promotion of the maintenance of biological diversity by monitoring 1. To participate in the further development, promotion and implementation the status of species and populations of conservation concern. of the World Conservation Strategy; to advise on the development of IUCN's Conservation Programme; to support the implementation of the • development and review of conservation action plans and priorities Programme' and to assist in the development, screening, and monitoring for species and their populations. -
University of Texas at Arlington Dissertation Template
EVOLUTIONARY RELATIONSHIPS IN SOME NORTHERN GROUPS OF THE DIRECT-DEVELOPING FROG GENUS CRAUGASTOR (ANURA: CRAUGASTORIDAE) by JEFFREY W. STREICHER Presented to the Faculty of the Graduate School of The University of Texas at Arlington in Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY THE UNIVERSITY OF TEXAS AT ARLINGTON May 2012 Copyright © by Jeffrey W. Streicher 2012 All Rights Reserved ACKNOWLEDGEMENTS During my time at UT Arlington I have been assisted by an outstanding community of individuals. First, I thank my fellow graduate students who have not only challenged me to be a better biologist, but also provided friendship and moral support. I thank Jesse Meik, Christian Cox, Coleman Sheehy III, Thomas Eimermacher, Brian Fontenot, Walter Schargel, Andrea Acevedo, Corey Roelke, Mike Logan, Matt Ingrasci, Jacobo Reyes-Velasco, Ben Anders, Utpal Smart, David Sanchez, Paul Pasichnyk, Alex Hall, and Matt Watson. Second, I thank my committee members; Eric Smith, Jon Campbell, Paul Chippindale, Esther Betrán, and Jeff Demuth, for their support and advice. Third, I thank the administrative staff; Linda Taylor, Gloria Burlingham, and Peggy Fisher for always answering my questions. I thank the following individuals for field companionship during our U.S.A., Mexico, Ecuador, South Africa, Costa Rica, India, and Guatemala trips: Coleman Sheehy III, Christian Cox, Thomas Eimermacher, Beryl Wilson, Jesse Meik, Matt Ingrasci, Mario Yanez, Carlos Vásquez Almazán, Gustavo Ruano Fajardo, Jacobo Reyes-Velasco, Oscar Flores-Villela, Virginia León-Règagnon, Elizabeth Martínez- Salizar, Elisa Cabrera-Guzman, Ruben Tovar, Paulino Ponce-Campos, Toni Arizmendi- Espinosa, Carl Franklin, Eric Smith, Jonathan Campbell, Butch Brodie Jr., and Robert Makowsky. -
Plasticity of Lung Development in the Amphibian, Xenopus Laevis
1324 Research Article Plasticity of lung development in the amphibian, Xenopus laevis Christopher S. Rose* and Brandon James James Madison University, Department of Biology, Biosciences 2028, Harrisonburg, VA 22807, USA *Author for correspondence ([email protected]) Biology Open 2, 1324–1335 doi: 10.1242/bio.20133772 Received 26th November 2012 Accepted 26th September 2013 Summary Contrary to previous studies, we found that Xenopus laevis role of mechanical forces in lung development. Lung tadpoles raised in normoxic water without access to air can recovery in AR frogs was unpredictable and did not routinely complete metamorphosis with lungs that are either correlate with behavioral changes. Its low frequency of severely stunted and uninflated or absent altogether. This is occurrence could be attributed to developmental, physical the first demonstration that lung development in a tetrapod and behavioral changes, the effects of which increase with can be inhibited by environmental factors and that a tetrapod size and age. Plasticity of lung inflation at tadpole stages and that relies significantly on lung respiration under unstressed loss of plasticity at postmetamorphic stages offer new insights conditions can be raised to forego this function without into the role of developmental plasticity in amphibian lung adverse effects. This study compared lung development in loss and life history evolution. untreated, air-deprived (AD) and air-restored (AR) tadpoles and frogs using whole mounts, histology, BrdU labeling of ß 2013. Published by The Company of Biologists Ltd. This cell division and antibody staining of smooth muscle actin. is an Open Access article distributed under the terms of We also examined the relationship of swimming and the Creative Commons Attribution License (http:// breathing behaviors to lung recovery in AR animals. -
Cryptic Diversity and Ranavirus Infection of a Critically Endangered Neotropical Frog Before and After Population Collapse
Cryptic diversity and ranavirus infection of a critically endangered Neotropical frog before and after population collapse Robert Puschendorf 1,7,8, Megan Wallace 2,7, María Marta Chavarría 3, Andrew Crawford 4, Felicity Wynne 1, Mairi Knight 1, Daniel Janzen5, Winnie Hallwachs 5, Caroline Palmer 1, Stephen J. Price 6 1 School of Biological and Marine Sciences, University of Plymouth, Devon, PL4 8AA, UK 2 Department of Zoology, University of Oxford, New Radcliffe House, Radcliffe Observatory Quarter, Woodstock Road, Oxford OX2 6GG, UK. Present address: Institute of Evolutionary Biology, University of Edinburgh, Ashworth Laboratories, Charlotte Auerbach Road Edinburgh, EH9 3FL, UK. 3 Programa de Investigación, Área de Conservación Guanacaste, Aptdo. 169-5000, Liberia, Costa Rica. 4 Departamento de Ciencias Biológicas, Universidad de los Andes, Bogotá, Colombia 5 Department of Biology, University of Pennsylvania, Philadelphia, PA 19104-6018, USA 6 UCL Genetics Institute, Gower Street, London, WC1E 6BT, UK Institute of Zoology, ZSL, Regents Park, London NW1 4RY, UK. 7 Shared first authorship 8 Corresponding author email: [email protected], phone: +441752584658 1 Abstract Mesoamerican amphibian declines in apparently pristine and protected habitats have been severe, especially at elevations above 500 m sea level and have been linked to emerging diseases and a changing climate. The Craugastor punctariolus species series of direct developing frogs is endemic to the region and used to be comprised of 33 species, seven of which have known populations at present. One of these, Craugastor ranoides, endemic to southern Nicaragua and Costa Rica, was historically found in cloud forest sites of Área de Conservación Guanacaste (ACG) in north-west Costa Rica and extended into dry forest sites 20 km distant. -
3Systematics and Diversity of Extant Amphibians
Systematics and Diversity of 3 Extant Amphibians he three extant lissamphibian lineages (hereafter amples of classic systematics papers. We present widely referred to by the more common term amphibians) used common names of groups in addition to scientifi c Tare descendants of a common ancestor that lived names, noting also that herpetologists colloquially refer during (or soon after) the Late Carboniferous. Since the to most clades by their scientifi c name (e.g., ranids, am- three lineages diverged, each has evolved unique fea- bystomatids, typhlonectids). tures that defi ne the group; however, salamanders, frogs, A total of 7,303 species of amphibians are recognized and caecelians also share many traits that are evidence and new species—primarily tropical frogs and salaman- of their common ancestry. Two of the most defi nitive of ders—continue to be described. Frogs are far more di- these traits are: verse than salamanders and caecelians combined; more than 6,400 (~88%) of extant amphibian species are frogs, 1. Nearly all amphibians have complex life histories. almost 25% of which have been described in the past Most species undergo metamorphosis from an 15 years. Salamanders comprise more than 660 species, aquatic larva to a terrestrial adult, and even spe- and there are 200 species of caecilians. Amphibian diver- cies that lay terrestrial eggs require moist nest sity is not evenly distributed within families. For example, sites to prevent desiccation. Thus, regardless of more than 65% of extant salamanders are in the family the habitat of the adult, all species of amphibians Plethodontidae, and more than 50% of all frogs are in just are fundamentally tied to water. -
Shifts in the Diversity of an Amphibian Community from a Premontane Forest of San Ramón, Costa Rica Cambios En La Diversidad De
DOI 10.15517/RBT.V67I2SUPL.37240 Artículo Shifts in the diversity of an amphibian community from a premontane forest of San Ramón, Costa Rica Cambios en la diversidad de una comunidad de anfibios en un bosque premontano de San Ramón, Costa Rica Víctor J. Acosta-Chaves1, 2* Víctor Madrigal-Elizondo3 Gerardo Chaves4 Brayan Morera-Chacón5 Adrián García-Rodríguez 4, 6 Federico Bolaños 4 1 Carrera de Turismo Ecológico, Universidad de Costa Rica Sede Atlántico, Recinto de Paraíso, Cartago, Costa Rica; [email protected]* 2 Red Mesoamericana y del Caribe para la Conservación de Anfibios y Reptiles. 3 Red de Áreas Protegidas, Universidad de Costa Rica, Sede Rodrigo Facio, San Pedro, Costa Rica; [email protected] 4 Escuela de Biología, Universidad de Costa Rica, San Pedro, 11501-2060 San José, Costa Rica; [email protected], [email protected] 5 Instituto Internacional para la Conservación y Manejo de Vida Silvestre, Universidad Nacional, Heredia, Costa Rica; [email protected] 6 Departamento de Zoología, Instituto de Biología, Universidad Nacional Autónoma de México, Mexico City, Mexico; [email protected] * Correspondence Received 05-X-2018 Corrected 18-I-2019 Accepted 06-II-2019 Abstract Biological communities are experiencing rapid shifts of composition in Neotropical ecosystems due to several factors causing population declines. However, emerging evidence has provided insights on the adaptive potential of multiple species to respond to illnesses and environmental pressures. In Costa Rica, the decline of amphibian populations is a remarkable example of these changes. Here we provide evidence of variation in the amphibian richness of a premontane forest of San Ramón (Costa Rica) across a ~30 year period. -
Craugastor Augusti) in New Mexico Mason J
University of New Mexico UNM Digital Repository Faculty and Staff ubP lications Museum of Southwestern Biology 11-30-2015 Final Report: Status of Barking Frog (Craugastor augusti) in New Mexico Mason J. Ryan Ian M. Latella Jacek Tomasz Giermakowski Howard Snell Follow this and additional works at: https://digitalrepository.unm.edu/msb_fsp Recommended Citation Ryan, M. J., Latella, I. M., Giermakowski, J. T., & Snell, H. (2015). Final Report: Status of Barking Frog (Craugastor augusti) in New Mexico. https://doi.org/10.25844/7922-3R81 This Technical Report is brought to you for free and open access by the Museum of Southwestern Biology at UNM Digital Repository. It has been accepted for inclusion in Faculty and Staff ubP lications by an authorized administrator of UNM Digital Repository. For more information, please contact [email protected]. Final Report: Status of Barking Frog (Craugastor augusti) in New Mexico Delivered to New Mexico Department of Game and Fish on November 30, 2015 Permanently archived in the University of New Mexico Institutional Repository (https://repository.unm.edu/ ) with the identifier http://hdl.handle.net/1928/33082 Project Work Order: #150422 Reporting period: 1 May 2015–30 Nov 2015 Authorship: Mason J Ryan, Ian M Latella, J Tomasz Giermakowski, Howard L Snell University of New Mexico and Museum of Southwestern Biology, Albuquerque, NM. [email protected], 505-277-5130 Suggested citation: Ryan, MJ, IM Latella, JT Giermakowski, HL Snell. 2015. Final Report: Status of Barking Frog (Craugastor augusti) in New Mexico. Submitted to New Mexico Department of Game and Fish; Project Work Order: #150422. Albuquerque, New Mexico: University of New Mexico, November 30, 2015. -
Full Text in Pdf Format
Vol. 45: 331–335, 2021 ENDANGERED SPECIES RESEARCH Published May 27 https://doi.org/10.3354/esr01138 Endang Species Res OPEN ACCESS NOTE First case of male alloparental care in amphibians: tadpole stealing in Darwin’s frogs Osvaldo Cabeza-Alfaro1, Andrés Valenzuela-Sánchez2,3,4, Mario Alvarado-Rybak2,5, José M. Serrano3,6, Claudio Azat2,* 1Zoológico Nacional, Pio Nono 450, Recoleta, Santiago 8420541, Chile 2Sustainability Research Centre & PhD Programme in Conservation Medicine, Faculty of Life Sciences, Universidad Andres Bello, Republica 440, Santiago 8370251, Chile 3ONG Ranita de Darwin, Ruta T-340 s/n, Valdivia 5090000, Chile 4Instituto de Conservación, Biodiversidad y Territorio, Facultad de Ciencias Forestales y Recursos Naturales, Universidad Austral de Chile, Casilla 567, Valdivia 5110027, Chile 5Núcleo de Ciencias Aplicadas en Ciencias Veterinarias y Agronómicas, Universidad de las Américas, Echaurren 140, Santiago 8370065, Chile 6Museo de Zoología ‘Alfonso L. Herrera’, Departamento Biología Evolutiva, Facultad de Ciencias, Universidad Nacional Autónoma de México, Circuito Exterior s/n, Ciudad Universitaria, Coyoacán, Mexico City 04510, Mexico ABSTRACT: Alloparental care, i.e. care directed at non-descendant offspring, has rarely been described in amphibians. Rhinoderma darwinii is an Endangered and endemic frog of the tem - perate forests of Chile and Argentina. This species has evolved a unique reproductive strategy whereby males brood their tadpoles within their vocal sacs (known as neomelia). Since 2009, the National Zoo of Chile has developed an ex situ conservation programme for R. darwinii, in which during reproduction, adults are kept in terraria in groups of 2 females with 2 males. In September 2018, one pair engaged in amplexus, with one of the males fertilizing the eggs. -
A Method to Distinguish Intensively Farmed from Wild Frogs
Received: 23 March 2016 | Revised: 30 January 2017 | Accepted: 6 February 2017 DOI: 10.1002/ece3.2878 ORIGINAL RESEARCH Stable isotope analyses—A method to distinguish intensively farmed from wild frogs Carolin Dittrich | Ulrich Struck | Mark-Oliver Rödel Museum für Naturkunde, Leibniz Institute for Evolution and Biodiversity Science, Berlin, Abstract Germany Consumption of frog legs is increasing worldwide, with potentially dramatic effects for Correspondence ecosystems. More and more functioning frog farms are reported to exist. However, Mark-Oliver Rödel, Museum für Naturkunde, due to the lack of reliable methods to distinguish farmed from wild- caught individuals, Leibniz Institute for Evolution and Biodiversity Science, Berlin, Germany. the origin of frogs in the international trade is often uncertain. Here, we present a new Email: [email protected] methodological approach to this problem. We investigated the isotopic composition of Funding information legally traded frog legs from suppliers in Vietnam and Indonesia. Muscle and bone tis- 15 13 18 Museum für Naturkunde Berlin; MfN sue samples were examined for δ N, δ C, and δ O stable isotope compositions, to Innovation fund; Leibniz Association′s Open Access Publishing Fund elucidate the conditions under which the frogs grew up. We used DNA barcoding (16S rRNA) to verify species identities. We identified three traded species (Hoplobatrachus rugulosus, Fejervarya cancrivora and Limnonectes macrodon); species identities were 15 18 partly deviating from package labeling. Isotopic values of δ N and δ O showed sig- 15 nificant differences between species and country of origin. Based on low δ N compo- sition and generally little variation in stable isotope values, our results imply that frogs from Vietnam were indeed farmed.