Amphibia: Gymnophiona: Dermophiidae)
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Chec List a Checklist of the Amphibians and Reptiles of San
Check List 10(4): 870–877, 2014 © 2014 Check List and Authors Chec List ISSN 1809-127X (available at www.checklist.org.br) Journal of species lists and distribution PECIES S OF A checklist * of the amphibians and reptiles of San Isidro de ISTS L Dota, Reserva Forestal Los Santos, Costa Rica Erick Arias and Federico Bolaños [email protected] Universidad de Costa Rica, Escuela de Biología, Museo de Zoología. San Pedro, 11501-2060, San José, Costa Rica. * Corresponding author. E-mail: Abstract: We present an inventory of amphibians and reptiles of San Isidro de Dota, northwest of the Cordillera de Talamanca in the Central Pacific of Costa Rica.Leptodactylus The study was insularum conduced from January to August 2012 in premontane wet Coloptychonforest from 689 rhombifer m to 800 m elevation. We found a total of 56 species, including 30 species of amphibians and 26 of reptiles. It results striking the presence of the frog , uncommon above 400 m elevation, and the lizard , a very uncommon species. DOI: 10.15560/10.4.870 Introduction datum, from 689 m to 800 N, 83°58′32.41″ W, WGS84et al. Lower Central America represents one of the regions m elevation). The region is dominated by premontane with the highest numberet al of amphibianset describedal. in the wet forest (Bolaños 1999) with several sites used Neotropics in relation to the area it represent (Savage for agriculture and pastures. The region presents the 2002; Boza-Oviedo . 2012; Hertz 2012). Much climate of the pacific slope of the Cordillera de Talamanca, of this richness of species iset associated al. -
BOA2.1 Caecilian Biology and Natural History.Key
The Biology of Amphibians @ Agnes Scott College Mark Mandica Executive Director The Amphibian Foundation [email protected] 678 379 TOAD (8623) 2.1: Introduction to Caecilians Microcaecilia dermatophaga Synapomorphies of Lissamphibia There are more than 20 synapomorphies (shared characters) uniting the group Lissamphibia Synapomorphies of Lissamphibia Integumen is Glandular Synapomorphies of Lissamphibia Glandular Skin, with 2 main types of glands. Mucous Glands Aid in cutaneous respiration, reproduction, thermoregulation and defense. Granular Glands Secrete toxic and/or noxious compounds and aid in defense Synapomorphies of Lissamphibia Pedicellate Teeth crown (dentine, with enamel covering) gum line suture (fibrous connective tissue, where tooth can break off) basal element (dentine) Synapomorphies of Lissamphibia Sacral Vertebrae Sacral Vertebrae Connects pelvic girdle to The spine. Amphibians have no more than one sacral vertebrae (caecilians have none) Synapomorphies of Lissamphibia Amphicoelus Vertebrae Synapomorphies of Lissamphibia Opercular apparatus Unique to amphibians and Operculum part of the sound conducting mechanism Synapomorphies of Lissamphibia Fat Bodies Surrounding Gonads Fat Bodies Insulate gonads Evolution of Amphibians † † † † Actinopterygian Coelacanth, Tetrapodomorpha †Amniota *Gerobatrachus (Ray-fin Fishes) Lungfish (stem-tetrapods) (Reptiles, Mammals)Lepospondyls † (’frogomander’) Eocaecilia GymnophionaKaraurus Caudata Triadobatrachus Anura (including Apoda Urodela Prosalirus †) Salientia Batrachia Lissamphibia -
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. -
A New Species of Skin-Feeding Caecilian and the First Report of Reproductive Mode in Microcaecilia (Amphibia: Gymnophiona: Siphonopidae)
A New Species of Skin-Feeding Caecilian and the First Report of Reproductive Mode in Microcaecilia (Amphibia: Gymnophiona: Siphonopidae) The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters. Citation Wilkinson, Mark, Emma Sherratt, Fausto Starace, and David J. Gower. 2013. A new species of skin-feeding caecilian and the first report of reproductive mode in Microcaecilia (amphibia: gymnophiona: siphonopidae). PLoS ONE 8(3): e57756. Published Version doi:10.1371/journal.pone.0057756 Accessed February 19, 2015 12:00:32 PM EST Citable Link http://nrs.harvard.edu/urn-3:HUL.InstRepos:10682457 Terms of Use This article was downloaded from Harvard University's DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA (Article begins on next page) A New Species of Skin-Feeding Caecilian and the First Report of Reproductive Mode in Microcaecilia (Amphibia: Gymnophiona: Siphonopidae) Mark Wilkinson1, Emma Sherratt1,2*, Fausto Starace3, David J. Gower1 1 Department of Zoology, The Natural History Museum, London, United Kingdom, 2 Department of Organismic and Evolutionary Biology and Museum of Comparative Zoology, Harvard University, Cambridge, Massachusetts United States of America, 3 BP 127, 97393 Saint Laurent du Maroni Cedex, French Guiana Abstract A new species of siphonopid caecilian, Microcaecilia dermatophaga sp. nov., is described based on nine specimens from French Guiana. The new species is the first new caecilian to be described from French Guiana for more than 150 years. -
Morphological Evolution and Modularity of the Caecilian Skull Carla Bardua1,2* , Mark Wilkinson1, David J
Bardua et al. BMC Evolutionary Biology (2019) 19:30 https://doi.org/10.1186/s12862-018-1342-7 RESEARCH ARTICLE Open Access Morphological evolution and modularity of the caecilian skull Carla Bardua1,2* , Mark Wilkinson1, David J. Gower1, Emma Sherratt3 and Anjali Goswami1,2 Abstract Background: Caecilians (Gymnophiona) are the least speciose extant lissamphibian order, yet living forms capture approximately 250 million years of evolution since their earliest divergences. This long history is reflected in the broad range of skull morphologies exhibited by this largely fossorial, but developmentally diverse, clade. However, this diversity of form makes quantification of caecilian cranial morphology challenging, with highly variable presence or absence of many structures. Consequently, few studies have examined morphological evolution across caecilians. This extensive variation also raises the question of degree of conservation of cranial modules (semi-autonomous subsets of highly-integrated traits) within this clade, allowing us to assess the importance of modular organisation in shaping morphological evolution. We used an intensive surface geometric morphometric approach to quantify cranial morphological variation across all 32 extant caecilian genera. We defined 16 cranial regions using 53 landmarks and 687 curve and 729 surface sliding semilandmarks. With these unprecedented high-dimensional data, we analysed cranial shape and modularity across caecilians assessing phylogenetic, allometric and ecological influences on cranial evolution, as well as investigating the relationships among integration, evolutionary rate, and morphological disparity. Results: We found highest support for a ten-module model, with greater integration of the posterior skull. Phylogenetic signal was significant (Kmult =0.87,p < 0.01), but stronger in anterior modules, while allometric influences were also significant (R2 =0.16,p < 0.01), but stronger posteriorly. -
Correction (934.7Kb)
Correction Correction: Population Genetics of the Sa˜o Tome´ Caecilian (Gymnophiona: Dermophiidae: Schistometopum thomense) Reveals Strong Geographic Structuring The PLOS ONE Staff The parameter name in the Materials and Methods section and Results section are incorrectly formatted. In all cases, the correct parameter name is Fu’s Fs. The genetic variability measure in the Results section is incorrectly formatted. The correct genetic variability measure is FST. The Figure 1 legend is incorrect. The word ‘‘Red’’ should be ‘‘Black’’ in the last sentence. The authors have provided a corrected version here. Citation: The PLOS ONE Staff (2014) Correction: Population Genetics of the Sa˜o Tome´ Caecilian (Gymnophiona: Dermophiidae: Schistometopum thomense) Reveals Strong Geographic Structuring. PLoS ONE 9(12): e116005. doi:10.1371/ journal.pone.0116005 Published December 15, 2014 Copyright: ß 2014 The PLOS ONE Staff. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. PLOS ONE | www.plosone.org 1 December 2014 | Volume 9 | Issue 12 | e116005 Figure 1. Schistometopum thomense collection localities, Sa˜o Tome´, Republic of Sa˜o Tome´ and Prı´ncipe. Numbers in parentheses indicate number of specimens available for genetic analyses. Legend indicates specimens used in Splits Tree, Bayesian, SAMOVA, and/or IMa2 analyses, or discussed by Nussbaum and Pfrender [36] in morphological comparisons. Dashed, red ovals indicate populations lumped for SAMOVA analyses. Photographs show examples of clear and flecked morphs as Schistometopum thomense and Schistometopum ‘‘ephele’’, respectively. Red star in lower left panel indicates relative position of Sa˜o Tome´ to continental Africa. -
Morphological Variation and Geographical Distribution of Luetkenotyphlus Brasiliensis (Gymnophiona: Siphonopidae)
Phyllomedusa 10(2):153–163, 2011 © 2011 Departamento de Ciências Biológicas - ESALQ - USP ISSN 1519-1397 Morphological variation and geographical distribution of Luetkenotyphlus brasiliensis (Gymnophiona: Siphonopidae) Tamí Mott1, Mário Ribeiro de Moura2, Adriano Oliveira Maciel3, and Renato Neves Feio2 1 Setor de Biodiversidade e Ecologia, Instituto de Ciências Biológicas e da Saúde, Universidade Federal de Alagoas, 57010-020, Maceió, AL, Brazil. E-mail: [email protected]. 2 Museu de Zoologia João Moojen, Departamento de Biologia Animal, Universidade Federal de Viçosa, 36570-000, Viçosa, MG, Brazil. 3 Departamento de Zoologia, Museu Paraense Emílio Goeldi, 66077-530, Belém, PA, Brazil. Abstract Morphological variation and geographical distribution of Luetkenotyphlus brasiliensis (Gymnophiona: Siphonopidae). The geographical distribution of Luetkenotyphlus brasiliensis is reviewed based on data from the literature and examination of specimens recently collected in Brazil. We also provide new information on variation of the vomerine diastema, and meristic and morphometric data for L. brasiliensis based on Brazilian specimens. Keywords: Brazil, caecilian, meristic data, morphometry, vomerine diastema. Resumo Variação morfológica e distribuição geográfica de Luetkenotyphlus brasiliensis (Gymnophiona: Siphonopidae). A distribuição geográfica de Luetkenotyphlus brasiliensis é revisada com base em dados de literatura e análise de espécimes recentemente coletados no Brasil. Informações inéditas sobre a variação do diastema vomeriano, dados -
First Record of Siphonops Paulensis Boettger, 1892 (Gymnophiona: Siphonopidae) in the State of Sergipe, Northeastern Brazil
10TH ANNIVERSARY ISSUE Check List the journal of biodiversity data NOTES ON GEOGRAPHIC DISTRIBUTION Check List 11(1): 1531, January 2015 doi: http://dx.doi.org/10.15560/11.1.1531 ISSN 1809-127X © 2015 Check List and Authors First record of Siphonops paulensis Boettger, 1892 (Gymnophiona: Siphonopidae) in the state of Sergipe, northeastern Brazil Daniel Oliveira Santana1*, Crizanto Brito De-Carvalho2, Evellyn Borges de Freitas2, Geziana Silva Siqueira Nunes2 and Renato Gomes Faria2 1 Universidade Federal da Paraíba, Programa de Pós Graduação em Ciências Biológicas (Zoologia). Cidade Universitária, Avenida Contorno da Cidade Universitária, s/nº, Castelo Branco. CEP 58059-900. João Pessoa, PB, Brazil 2 Universidade Federal de Sergipe, Programa de Pós-graduação em Ecologia e Conservação. Cidade Universitária Prof. José Aloísio de Campos, Avenida Marechal Rondon, s/nº, Jardim Rosa Elze. CEP 49100-000. São Cristóvão, SE, Brazil * Corresponding author: E-mail: [email protected] Abstract: Siphonopidae is represented by 25 caecilians spe- even been found in urban gardens. It is oviparous with terrestrial cies in South America. In Brazil, Siphonops paulensis is found eggs and direct development, and not dependent on water for in the states of Maranhão, Rio Grande do Norte, Bahia, Tocan- breeding (Aquino et al. 2004). We present a distribution map tins, Goiás, Mato Grosso, Mato Grosso do Sul, Minas Gerais, (Figure 1) and data in Table 1 of the current known distribution São Paulo, Rio de Janeiro, Rio Grande do Sul, and in the Dis- of this species based on literature. trito Federal. Herein, we report the first record of Siphonops Herein, we report the first record ofSiphonops paulensis paulensis in the state of Sergipe, Brazil, Simão Dias municipal- (Figure 2) for the state of Sergipe, Brazil. -
Published Version
PUBLISHED VERSION Mark Wilkinson, Emma Sherratt, Fausto Starace, David J. Gower A new species of skin-feeding caecilian and the first report of reproductive mode in Microcaecilia (Amphibia: Gymnophiona: Siphonopidae) PLoS ONE, 2013; 8(3):e57756-1-e57756-11 © 2013 Wilkinson et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Originally published at: http://doi.org/10.1371/journal.pone.0057756 PERMISSIONS http://creativecommons.org/licenses/by/3.0/ 29 June 2017 http://hdl.handle.net/2440/106056 A New Species of Skin-Feeding Caecilian and the First Report of Reproductive Mode in Microcaecilia (Amphibia: Gymnophiona: Siphonopidae) Mark Wilkinson1, Emma Sherratt1,2*, Fausto Starace3, David J. Gower1 1 Department of Zoology, The Natural History Museum, London, United Kingdom, 2 Department of Organismic and Evolutionary Biology and Museum of Comparative Zoology, Harvard University, Cambridge, Massachusetts United States of America, 3 BP 127, 97393 Saint Laurent du Maroni Cedex, French Guiana Abstract A new species of siphonopid caecilian, Microcaecilia dermatophaga sp. nov., is described based on nine specimens from French Guiana. The new species is the first new caecilian to be described from French Guiana for more than 150 years. It differs from all other Microcaecilia in having fewer secondary annular grooves and/or in lacking a transverse groove on the dorsum of the first collar. Observations of oviparity and of extended parental care in M. dermatophaga are the first reproductive mode data for any species of the genus. -
Towards Evidence-Based Husbandry for Caecilian Amphibians: Substrate Preference in Geotrypetes Seraphini (Amphibia: Gymnophiona: Dermophiidae)
RESEARCH ARTICLE The Herpetological Bulletin 129, 2014: 15-18 Towards evidence-based husbandry for caecilian amphibians: Substrate preference in Geotrypetes seraphini (Amphibia: Gymnophiona: Dermophiidae) BENJAMIN TAPLEY1*, ZOE BRYANT1, SEBASTIAN GRANT1, GRANT KOTHER1, YEDRA FEL- TRER1, NIC MASTERS1, TAINA STRIKE1, IRI GILL1, MARK WILKINSON2 & DAVID J GOWER2 1Zoological Society of London, Regents Park, London NW1 4RY 2Department of Life Sciences, The Natural History Museum, Cromwell Road, London, SW7 5BD *Corresponding author email: [email protected] ABSTRACT - Maintaining caecilians in captivity provides opportunities to study life-history, behaviour and reproductive biology and to investigate and to develop treatment protocols for amphibian chytridiomycosis. Few species of caecilians are maintained in captivity and little has been published on their husbandry. We present data on substrate preference in a group of eight Central African Geotrypetes seraphini (Duméril, 1859). Two substrates were trialled; coir and Megazorb (a waste product from the paper making industry). G. seraphini showed a strong preference for the Megazorb. We anticipate this finding will improve the captive management of this and perhaps also other species of fossorial caecilians, and stimulate evidence-based husbandry practices. INTRODUCTION (Gower & Wilkinson, 2005) and little has been published on the captive husbandry of terrestrial caecilians (Wake, 1994; O’ Reilly, 1996). A basic parameter in terrestrial The paucity of information on caecilian ecology and caecilian husbandry is substrate, but data on tolerances and general neglect of their conservation needs should be of preferences in the wild or in captivity are mostly lacking. concern in light of global amphibian declines (Alford & Terrestrial caecilians are reported from a wide range of Richards 1999; Stuart et al., 2004; Gower & Wilkinson, soil pH (Gundappa et al., 1981; Wake, 1994; Kupfer et 2005). -
The Amphibians of South-Eastern Republic of Guinea 99-118 ©Österreichische Gesellschaft Für Herpetologie E.V., Wien, Austria, Download Unter
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Herpetozoa Jahr/Year: 2004 Band/Volume: 17_3_4 Autor(en)/Author(s): Rödel Mark-Oliver, Böhme Wolfgang, Bangoura Mohamed Alhassane Artikel/Article: The amphibians of south-eastern Republic of Guinea 99-118 ©Österreichische Gesellschaft für Herpetologie e.V., Wien, Austria, download unter www.biologiezentrum.at HERPETOZOA 17 (3/4): 99 - 118 99 Wien, 30. Dezember 2004 The amphibians of south-eastern Republic of Guinea (Amphibia: Gymnophiona, Anura) Die Amphibien.Südostguineas (Amphibia: Gymnophiona, Anura) MARK-OLIVER RODEL & MOHAMED ALHASSANE BANGOURA & WOLFGANG BÖHME KURZFASSUNG Wir berichten über die Amphibienfauna aus sechs Wald- und Berggebieten in Südostguinea. Drei der Gebiete (Déré, Diécké, Mont Béro) wurden im Rahmen eines kürzlich von Conservation International organisierten "Rapid Assessment Program" (RAP) untersucht. Für die übrigen drei Gebiete (Nimba Berge, Ziama, Pic de Fon) werteten wir Literaturdaten aus und untersuchten Belegexemplare in der Sammlung des Museums Koenig in Bonn (ZFMK). Insgesamt listen wir 73 für Südostguinea nachgewiesene Amphibienarten auf. Die Anzahl der pro Gebiet nachgewiesenen Arten reichte von 29 bis 58. Der Prozentsatz, der für Oberguinea endemischen Arten (insgesamt 39) pro Gebiet, schwankte von 42 bis 53 %. Einige Arten werden von uns detaillierter diskutiert. Der hohe Anteil von Störungsanzeigern (farmbush species) in allen untersuchten Gebieten ist ein untrügliches Zeichen für die be- reits deutlich fortgeschrittene Walddegradation, am dramatischsten sichtbar in Déré. Wir unterstreichen die Bedeu- tung von Wald-Guinea als eines der artenreichsten Gebiete Afrikas und fordern nachdrücklich einen intensiveren Schutz der verbliebenen Wälder und eine gründliche Untersuchung der vielen endemischen Amphibienarten über die nahezu keine Daten verfügbar sind. -
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.