Aromobates Meridensis, an Endangered
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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. -
Advertisement Call of Pratt's Rocket Frog, Colostethus Pratti, from The
SALAMANDRA 56(4): 395–400 SALAMANDRA 30 October 2020 ISSN 0036–3375 Correspondence German Journal of Herpetology Correspondence Advertisement call of Pratt’s rocket frog, Colostethus pratti, from the western Andes of Colombia (Anura: Dendrobatidae) Juan David Jiménez-Bolaño1, Andrés Camilo Montes-Correa1, Franziska Leonhardt2 & Juan Manuel Renjifo1 1) Grupo de Investigación en Manejo & Conservación de Fauna, Flora & Ecosistemas Estratégicos Neotropicales (MIKU), Universidad del Magdalena, Santa Marta, Colombia 2) Museum of Zoology, Senckenberg Natural History Collections Dresden, A. B. Meyer Building, 01109 Dresden, Germany Corresponding author: Andrés Camilo Montes-Correa, e-mail: [email protected] Manuscript received: 22 July 2019 Accepted: 14 April 2020 by Stefan Lötters Northwestern South America is one of the biologically most phibian checklists (Cochran & Goin 1970, Ruiz-Car- diverse yet least known regions of the world. The Tropi- ranza et al. 1994, Acosta-Galvis 2000, Lynch & Suá- cal Andes and Chocó-Tumbes-Magdalena ecoregions, two rez-Mayorga 2004, Ballesteros-Correa et al. 2019). hotspots with high degrees of endemism and conservation The most recent information onC. pratti in Colombia con- priority (Myers et al. 2000, Rodríguez-Mahecha et al. cerns its altitudinal distribution, relative abundance, and 2004), are part of this region. Especially the Chocoan low- natural history in the northernmost part of the western lands and the western Andes of Colombia are areas with Andes, at the Serranía de San Jerónimo, Departamento de exceptional high amphibian diversity and many endemic Córdoba (Romero-Martínez et al. 2008, Ballesteros- taxa (e.g., Lynch et al. 1997, Lynch & Suárez-Mayorga Correa et al. 2019). To the best of our knowledge, there is 2004, Armesto & Señaris 2017). -
Chromosome Analysis of Five Brazilian
c Indian Academy of Sciences RESEARCH ARTICLE Chromosome analysis of five Brazilian species of poison frogs (Anura: Dendrobatidae) PAULA CAMARGO RODRIGUES1, ODAIR AGUIAR2, FLÁVIA SERPIERI1, ALBERTINA PIMENTEL LIMA3, MASAO UETANEBARO4 and SHIRLEI MARIA RECCO-PIMENTEL1∗ 1Departamento de Anatomia, Biologia Celular e Fisiologia, Instituto de Biologia, Universidade Estadual de Campinas, 13083-863 Campinas, São Paulo, Brazil 2Departamento de Biociências, Universidade Federal de São Paulo, Campus Baixada Santista, 11060-001 Santos, São Paulo, Brazil 3Coordenadoria de Pesquisas em Ecologia, Instituto Nacional de Pesquisas do Amazonas, 69011-970 Manaus, Amazonas, Brazil 4Departamento de Biologia, Universidade Federal de Mato Grosso do Sul, 70070-900 Campo Grande, Mato Grosso do Sul, Brazil Abstract Dendrobatid frogs have undergone an extensive systematic reorganization based on recent molecular findings. The present work describes karyotypes of the Brazilian species Adelphobates castaneoticus, A. quinquevittatus, Ameerega picta, A. galactonotus and Dendrobates tinctorius which were compared to each other and with previously described related species. All karyotypes consisted of 2n = 18 chromosomes, except for A. picta which had 2n = 24. The karyotypes of the Adelphobates and D. tinctorius species were highly similar to each other and to the other 2n = 18 previously studied species, revealing conserved karyotypic characteristics in both genera. In recent phylogenetic studies, all Adelphobates species were grouped in a clade separated from the Dendrobates species. Thus, we hypothesized that their common karyotypic traits may have a distinct origin by chromosome rearrangements and mutations. In A. picta, with 2n = 24, chromosome features of pairs from 1 to 8 are shared with other previously karyotyped species within this genus. Hence, the A. -
Anura: Dendrobatidae: Anomaloglossus) from the Orinoquian Rainforest, Southern Venezuela
TERMS OF USE This pdf is provided by Magnolia Press for private/research use. Commercial sale or deposition in a public library or website is prohibited. Zootaxa 2413: 37–50 (2010) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2010 · Magnolia Press ISSN 1175-5334 (online edition) A new dendrobatid frog (Anura: Dendrobatidae: Anomaloglossus) from the Orinoquian rainforest, southern Venezuela CÉSAR L. BARRIO-AMORÓS1,4, JUAN CARLOS SANTOS2 & OLGA JOVANOVIC3 1,4 Fundación AndígenA, Apartado postal 210, 5101-A Mérida, Venezuela 2University of Texas at Austin, Integrative Biology, 1 University Station C0930 Austin TX 78705, USA 3Division of Evolutionary Biology, Technical University of Braunschweig, Spielmannstr 8, 38106 Braunschweig, Germany 4Corresponding author. E-mail: [email protected]; [email protected] Abstract A new species of Anomaloglossus is described from the Venezuelan Guayana; it is the 21st described species of Anomaloglossus from the Guiana Shield, and the 15th from Venezuela. This species inhabits rainforest on granitic substrate on the northwestern edge of the Guiana Shield (Estado Amazonas, Venezuela). The new species is distinguished from congeners by sexual dimorphism, its unique male color pattern (including two bright orange parotoid marks and two orange paracloacal spots on dark brown background), call characteristics and other morphological features. Though to the new species is known only from the northwestern edge of the Guiana Shield, its distribution may be more extensive, as there are no significant biogeographic barriers isolating the type locality from the granitic lowlands of Venezuela. Key words: Amphibia, Dendrobatidae, Anomaloglossus, Venezuela, Guiana Shield Resumen Se describe una nueva especie de Anomaloglossus de la Guayana venezolana, que es la vigesimoprimera descrita del Escudo Guayanés, y la decimoquinta para Venezuela. -
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. -
Amphibian Ark Number 43 Keeping Threatened Amphibian Species Afloat June 2018
AArk Newsletter NewsletterNumber 43, June 2018 amphibian ark Number 43 Keeping threatened amphibian species afloat June 2018 In this issue... Reintroduction of the Northern Pool Frog to the UK - Progress Report, April 2018 ............... 2 ® Establishment of a captive breeding program for the Kroombit Tinkerfrog .............................. 4 In situ conservation of the Lemur Leaf Frog through habitat improvement and forest management practices in the Guayacán Rainforest Reserve in Costa Rica .................... 6 Neotropical amphibian biology, management and conservation course .................................. 8 Donation provides for equipment upgrades within the Biogeos Foundation facilities, at the Rescue of Endangered Venezuelan Amphibians program in Venezuela ................... 9 New AArk Conservation Grants program, and call for applications .................................. 10 Amphibian Advocates - José Alfredo Hernández Díaz, Africam Safari, Mexico ........ 11 Amphibian Advocates - Dr. Phil Bishop, Co-Chair IUCN SSC ASG............................... 12 AArk Newsletter - Instructions for authors ...... 13 A private donation helps the Valcheta Frog program in Argentina ...................................... 14 A rich food formula to raise tadpoles in captivity........................................................... 16 Vibicaria Conservation Program: creation of an ex situ model for a rediscovered species in Costa Rica ...................................................... 18 Reproduction of Dendropsophus padreluna at -
Ecology and Evolution of Phytotelm- Jreeding Anurans
* ECOLOGY AND EVOLUTION OF PHYTOTELM- JREEDING ANURANS Richard M. Lehtinen Editor MISCELLANEOUS PUBLICATIONS I--- - MUSEUM OF ZOOLOGY, UNIVERSITY OF MICHIGAN, NO. 193 Ann Ahr, November, 2004 PUBLICATIONS OF THE MUSEUM OF ZQOLOGY, UNIVERSITY OF MICHIGAN NO. 192 J. B. BURCII,Editot* Ku1.1: SI.EFANOAND JANICEPAPPAS, Assistant Editoras The publications of the Museum of Zoology, The University of Michigan, consist primarily of two series-the Miscellaneous P~rhlicationsand the Occasional Papers. Both serics were founded by Dr. Bryant Walker, Mr. Bradshaw H. Swales, and Dr. W. W. Newcomb. Occasionally the Museum publishes contributions outside of thesc series; beginning in 1990 these are titled Special Publications and are numbered. All s~tbmitledmanuscripts to any of the Museum's publications receive external review. The Occasiontrl Papers, begun in 1913, sellie as a mcdium for original studies based prii~cipallyupon the collections in the Museum. They are issued separately. When a sufficient number of pages has been printed to make a volume, a title page, table of contents, and an index are supplied to libraries and individuals on the mailing list for the series. The Mi.scelluneous Puhlicutions, initiated in 1916, include monographic studies, papers on field and museum techniques, and other contributions not within the scope of the Occasional Papers, and are publislled separately. It is not intended that they bc grouped into volumes. Each number has a title page and, when necessary, a table of contents. A complete list of publications on Mammals, Birds, Reptiles and Amphibians, Fishes, Insects, Mollusks, and other topics is avail- able. Address inquiries to Publications, Museum of Zoology, The University of Michigan, Ann Arbor, Michigan 48 109-1079. -
Reproductive Biology of Ameerega Trivittata(Anura: Dendrobatidae)
ACTA AMAZONICA http://dx.doi.org/10.1590/1809-4392201305384 Reproductive biology of Ameerega trivittata (Anura: Dendrobatidae) in an area of terra firme forest in eastern Amazonia Ellen Cristina Serrão ACIOLI1 * , Selvino NECKEL-OLIVEIRA2 ¹ Universidade Federal do Pará/Museu Paraense Emílio Goeldi, Programa de Pós Graduação em Zoologia, Av. Perimetral 1901/1907, Terra Firme, 66017-970, Belém, Pará, Brasil. ² Universidade Federal de Santa Catarina, Departamento de Ecologia e Zoologia, Centro de Ciências Biológicas, 88040-970, Florianópolis, Santa Catarina, Brasil. * Corresponding author: [email protected] ABSTRACT The reproductive success of tropical amphibians is influenced by factors such as body size and the characteristics of breeding sites. Data on reproductive biology are important for the understanding of population dynamics and the maintenance of species. The objectives of the present study were to examine the abundance ofAmeerega trivittata, analyze the use of microhabitats by calling males and the snout-vent length (SVL) of breeding males and females, the number of tadpoles carried by the males and mature oocytes in the females, as well as the relationship between the SVL of the female and both the number and mean size of the mature oocytes found in the ovaries. Three field trips were conducted between January and September, 2009. A total of 31 plots, with a mean area of 2.3 ha, were surveyed, resulting in records of 235 individuals, with a mean density of 3.26 individuals per hectare. Overall, 66.1% of the individuals sighted were located in the leaf litter, while 17.4% were perched on decaying tree trunks on the forest floor, 15.7% on the aerial roots ofCecropia trees, and 0.8% on lianas. -
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. -
Two New Endangered Species of Anomaloglossus (Anura: Aromobatidae) from Roraima State, Northern Brazil
Zootaxa 3926 (2): 191–210 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2015 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3926.2.2 http://zoobank.org/urn:lsid:zoobank.org:pub:BCA3901A-DF07-4FAF-8386-C24649557313 Two new endangered species of Anomaloglossus (Anura: Aromobatidae) from Roraima State, northern Brazil ANTOINE FOUQUET1,2,8, SERGIO MARQUES SOUZA2, PEDRO M. SALES NUNES2,3, PHILIPPE J. R. KOK4,5, FELIPE FRANCO CURCIO2,6, CELSO MORATO DE CARVALHO7, TARAN GRANT2 & MIGUEL TREFAUT RODRIGUES2 1CNRS Guyane USR3456, Immeuble Le Relais, 2 Avenue Gustave Charlery, 97300, Cayenne, French Guiana 2Universidade de São Paulo, Instituto de Biociências, Departamento de Zoologia, Caixa Postal 11.461,CEP 05508-090, São Paulo, SP, Brazil 3Universidade Federal de Pernambuco, Centro de Ciências Biológicas, Departamento de Zoologia, Av. Professor Moraes Rego, s/n. Cidade Universitária CEP 50670-901, Recife, PE, Brazil 4Biology Department, Amphibian Evolution Lab, Vrije Universiteit Brussel, 2 Pleinlaan, B- 1050 Brussels, Belgium 5Department of Recent Vertebrates, Royal Belgian Institute of Natural Sciences, 29 rue Vautier, B- 1000 Brussels, Belgium 6Universidade Federal de Mato Grosso, Instituto de Biociências, Departamento de Biologia e Zoologia, CEP 78060-900, Cuiaba MT, Brazil 7INPA Núcleo de Pesquisas de Roraima (INPA/NPRR), Rua Coronel Pinto 315 – Centro, 69301-970, Boa Vista, RR, Brazil 8Corresponding author. E-mail: [email protected] Abstract We describe two new species of Anomaloglossus from Roraima State, Brazil, that are likely endemic to single mountains currently isolated among lowland forest and savanna ecosystems. The first species, Anomaloglossus tepequem sp. -
The Herpetological Journal
Volume 16, Number 4 October 2006 ISSN 0268-0130 THE HERPETOLOGICAL JOURNAL Published by the BRITISH HERPETOLOGICAL SOCIETY The Herpetological Journal is published quarterly by the British Herpetological Society and is issued free to members. Articles are listed in Current Awareness in Biological Sciences, Current Contents, Science Citation Index and Zoological Record. Applications to purchase copies and/or fo r details of membership should be made to the Hon. Secretary, British Herpetological Society, The Zoological Society of London, Regent's Park, London NWI 4RY, UK. Instructions to authors are printed inside the back cover. All contributions should be addressed to the Scientific Editor (address below). Scientific Editor: Wolfgang Wlister, School of Biological Sciences, University of Wales, Bangor, Gwynedd, LL57 2UW, UK. E-mail: [email protected] Associate Scientifi c Editors: J. W. Arntzen (Leiden), R. Brown (Liverpool) Managing Editor: Richard A. Griffi ths, The Durrell Institute of Conservation and Ecology, Marlowe Building, University of Kent, Canterbury, Kent, CT2 7NR, UK. E-maiI: R. A. G riffi [email protected]. u k Associate Ma naging Editors: M. Dos Santos, J. McKay, M. Lock Editorial Board: Donald Broadley (Zimbabwe) John Cooper (Trinidad and Tobago) John Davenport (Cork ) Andrew Gardner (Abu Dhabi) Tim Halliday (Milton Keynes) Michael Klemens (New York ) Colin McCarthy (London) Andrew Milner (London) Richard Tinsley (Bristol) Copyright It is a fu ndamental condition that submitted manuscripts have not been published and will not be simultaneously submitted or published elsewhere. By submitting a manu script, the authors agree that the copyright fo r their article is transferred to the publisher if and when the article is accepted fo r publication. -
Myers 1987:304. Dendrobates Bombetes: Jungfer, Lötters, And
1 AMPHIBIA: ANURA: DENDROBATIDAE Andinobates bombetes Catalogue of American Amphibians and Minyobates bombetes: Myers 1987:304. Reptiles 926 Dendrobates bombetes: Jungfer, Lötters, and Jörgens 2000:11. F. Vargas-Salinas, M. A. Atehortua-Vallejo, L. Ranitomeya bombetes: Grant, Frost, Caldwell, F. Arcila-Pérez, G. M. Jiménez-Vargas, Gagliardo, Haddad, Kok, Means, Noonan, C. González-Acosta, S. Casas-Cardona, Schargel, and Wheeler 2006:171. and A. Grajales-Echeverry. 2020. Andinobates bombetes: Brown, Twomey, Andinobates bombetes. Amézquita, de Souza, Caldwell, Lötters, May, Melo-Sampaio, Mejía-Vargas, Pe- Andinobates bombetes (Myers and Daly) rez-Peña, Pepper, Poelman, Sanchez-Ro- Rubí poison frog driguez, and Summers 2011:36. Dendrobates bombetes Myers and Daly CONTENT. No subspecies are recognized. 1980:2. Type locality: “mountains above south side of Lago de Calima, 1580–1600 DESCRIPTION. Individuals of Andinobates meters elevation, about 2 km.,{sic} airline bombetes have a body size (snout-vent length, southwest of Puente Tierra (village), De- SVL) between 16.7– 21.5 mm, with no sexual partment of Valle del Cauca, Colombia.” dimorphism in body size (males: mean SVL Holotype, American Museum of Natural = 17.8 ± 0.1 mm SD, range: 16.7–21.5 mm; History, AMNH 102601, adult female, N = 28; females: mean SVL = 18.6 ± 0.1 mm collected by C. W. Myers, J. W. Daly and SD, range: 17.2–19.8 mm; N = 19) (Myers and E. B. de Bernal on 21 November 1976 (not Daly 1980; Suárez-Mayorga 1999; Vargas-Sa- examined by authors). linas and Amézquita 2013). In adults of Andi- Figure 1. Male of Andinobates bombetes from Finca El Placer, in the municipality of Filandia, depart- ment of Quindío, Colombia.