Little Is Known About the Diet of Caecilians Relative to Other Tetrapods
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Vertebrates, Overview
VERTEBRATES, OVERVIEW Carl Gans* and Christopher J. Bell† *Department of Integrative Biology, University of Texas at Austin and †Department of Geological Sciences, University of Texas at Austin I. Introduction neurectoderm An embryonic tissue that gives rise to II. General Vertebrate Characteristics the central tube of the nervous system. III. Early Chordate and Vertebrate History notochord A stiff, flexible, longitudinal rod running IV. Vertebrate Classification along the middorsal portion of the chordate body. V. Definitions and Diagnoses of Major Chordate It is situated dorsal to the coelom and ventral to the Groups central tube of the nervous system. pharynx The anterior portion of the alimentary canal, characterized by lateral buds that provide skeletal GLOSSARY support for the gill region. tuberculum interglenoideum An anterior projection of chordate A member of the group Chordata. The the first (cervical) vertebra in salamanders. The tu- Chordata includes the most recent common ancestor berculum interglenoideum bears articular facets that of tunicates and cephalochordates and all of that insert into the foramen magnum of the skull and ancestor’s descendants. Tunicates, lancelets, hag- provide additional articulation points between the fishes, and vertebrates are all chordates. skull and the vertebral column. ectoderm An embryonic tissue that provides the future outside layer of the animal. ectothermy A method of body temperature control in which the animal utilizes external sources for gaining VERTEBRATES INCLUDE ALL the fishes, amphibians, and giving up heat, thus achieving temperature con- reptiles, birds, and mammals. These animals are united trol without affecting metabolic rate. in a more inclusive group, the Chordata, that includes endothermy A method of body temperature control in the closest living relatives of vertebrates, the hagfishes, which the animal modifies its metabolic rate to lancelets, and tunicates. -
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. -
The Care and Captive Breeding of the Caecilian Typhlonectes Natans
HUSBANDRY AND PROPAGATION The care and captive breeding of the caecilian Typhlonectes natans RICHARD PARKINSON Ecology UK, 317 Ormskirk Road, Upholland, Skelmersdale, Lancashire, UK E-mail: [email protected] riAECILIANS (Apoda) are the often overlooked Many caecilians have no larval stage and, while third order of amphibians and are not thought some lay eggs, many including Typhlonectes natans to be closely-related to either Anurans or Urodelans. give birth to live young after a long pregnancy. Despite the existence of over 160 species occurring Unlike any other amphibian (or reptile) this is a true throughout the tropics (excluding Australasia and pregnancy in which the membranous gills of the Madagascar), relatively little is known about them. embryo functions like the placenta in mammals, so The earliest known fossil caecilian is Eocaecilia that the mother can supply the embryo with oxygen. micropodia, which is dated to the early Jurassic The embryo consumes nutrients secreted by the Period approximately 240 million years ago. uterine walls using specialized teeth for the Eocaecilia micropodia still possessed small but purpose. well developed legs like modem amphiumas and sirens. The worm-like appearance and generally Captive Care subterranean habits of caecilians has often led to In March 1995 I acquired ten specimens of the their dismissal as primitive and uninteresting. This aquatic caecilian Typhlonectes natans (identified by view-point is erroneous. Far from being primitive, cloacae denticulation after Wilkinson, 1996) which caecilians are highly adapted to their lifestyle. had been imported from Guyana. I immediately lost 7),phlonectes natans are minimalist organisms two as a result of an ill-fitting aquarium lid. -
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 -
Bioseries12-Amphibians-Taita-English
0c m 12 Symbol key 3456 habitat pond puddle river stream 78 underground day / night day 9101112131415161718 night altitude high low vegetation types shamba forest plantation prelim pages ENGLISH.indd ii 2009/10/22 02:03:47 PM SANBI Biodiversity Series Amphibians of the Taita Hills by G.J. Measey, P.K. Malonza and V. Muchai 2009 prelim pages ENGLISH.indd Sec1:i 2009/10/27 07:51:49 AM SANBI Biodiversity Series The South African National Biodiversity Institute (SANBI) was established on 1 September 2004 through the signing into force of the National Environmental Management: Biodiversity Act (NEMBA) No. 10 of 2004 by President Thabo Mbeki. The Act expands the mandate of the former National Botanical Institute to include responsibilities relating to the full diversity of South Africa’s fauna and ora, and builds on the internationally respected programmes in conservation, research, education and visitor services developed by the National Botanical Institute and its predecessors over the past century. The vision of SANBI: Biodiversity richness for all South Africans. SANBI’s mission is to champion the exploration, conservation, sustainable use, appreciation and enjoyment of South Africa’s exceptionally rich biodiversity for all people. SANBI Biodiversity Series publishes occasional reports on projects, technologies, workshops, symposia and other activities initiated by or executed in partnership with SANBI. Technical editor: Gerrit Germishuizen Design & layout: Elizma Fouché Cover design: Elizma Fouché How to cite this publication MEASEY, G.J., MALONZA, P.K. & MUCHAI, V. 2009. Amphibians of the Taita Hills / Am bia wa milima ya Taita. SANBI Biodiversity Series 12. South African National Biodiversity Institute, Pretoria. -
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. -
Tetrapod Biostratigraphy and Biochronology of the Triassic–Jurassic Transition on the Southern Colorado Plateau, USA
Palaeogeography, Palaeoclimatology, Palaeoecology 244 (2007) 242–256 www.elsevier.com/locate/palaeo Tetrapod biostratigraphy and biochronology of the Triassic–Jurassic transition on the southern Colorado Plateau, USA Spencer G. Lucas a,⁎, Lawrence H. Tanner b a New Mexico Museum of Natural History, 1801 Mountain Rd. N.W., Albuquerque, NM 87104-1375, USA b Department of Biology, Le Moyne College, 1419 Salt Springs Road, Syracuse, NY 13214, USA Received 15 March 2006; accepted 20 June 2006 Abstract Nonmarine fluvial, eolian and lacustrine strata of the Chinle and Glen Canyon groups on the southern Colorado Plateau preserve tetrapod body fossils and footprints that are one of the world's most extensive tetrapod fossil records across the Triassic– Jurassic boundary. We organize these tetrapod fossils into five, time-successive biostratigraphic assemblages (in ascending order, Owl Rock, Rock Point, Dinosaur Canyon, Whitmore Point and Kayenta) that we assign to the (ascending order) Revueltian, Apachean, Wassonian and Dawan land-vertebrate faunachrons (LVF). In doing so, we redefine the Wassonian and the Dawan LVFs. The Apachean–Wassonian boundary approximates the Triassic–Jurassic boundary. This tetrapod biostratigraphy and biochronology of the Triassic–Jurassic transition on the southern Colorado Plateau confirms that crurotarsan extinction closely corresponds to the end of the Triassic, and that a dramatic increase in dinosaur diversity, abundance and body size preceded the end of the Triassic. © 2006 Elsevier B.V. All rights reserved. Keywords: Triassic–Jurassic boundary; Colorado Plateau; Chinle Group; Glen Canyon Group; Tetrapod 1. Introduction 190 Ma. On the southern Colorado Plateau, the Triassic– Jurassic transition was a time of significant changes in the The Four Corners (common boundary of Utah, composition of the terrestrial vertebrate (tetrapod) fauna. -
Western Ghats & Sri Lanka Biodiversity Hotspot
Ecosystem Profile WESTERN GHATS & SRI LANKA BIODIVERSITY HOTSPOT WESTERN GHATS REGION FINAL VERSION MAY 2007 Prepared by: Kamal S. Bawa, Arundhati Das and Jagdish Krishnaswamy (Ashoka Trust for Research in Ecology & the Environment - ATREE) K. Ullas Karanth, N. Samba Kumar and Madhu Rao (Wildlife Conservation Society) in collaboration with: Praveen Bhargav, Wildlife First K.N. Ganeshaiah, University of Agricultural Sciences Srinivas V., Foundation for Ecological Research, Advocacy and Learning incorporating contributions from: Narayani Barve, ATREE Sham Davande, ATREE Balanchandra Hegde, Sahyadri Wildlife and Forest Conservation Trust N.M. Ishwar, Wildlife Institute of India Zafar-ul Islam, Indian Bird Conservation Network Niren Jain, Kudremukh Wildlife Foundation Jayant Kulkarni, Envirosearch S. Lele, Centre for Interdisciplinary Studies in Environment & Development M.D. Madhusudan, Nature Conservation Foundation Nandita Mahadev, University of Agricultural Sciences Kiran M.C., ATREE Prachi Mehta, Envirosearch Divya Mudappa, Nature Conservation Foundation Seema Purshothaman, ATREE Roopali Raghavan, ATREE T. R. Shankar Raman, Nature Conservation Foundation Sharmishta Sarkar, ATREE Mohammed Irfan Ullah, ATREE and with the technical support of: Conservation International-Center for Applied Biodiversity Science Assisted by the following experts and contributors: Rauf Ali Gladwin Joseph Uma Shaanker Rene Borges R. Kannan B. Siddharthan Jake Brunner Ajith Kumar C.S. Silori ii Milind Bunyan M.S.R. Murthy Mewa Singh Ravi Chellam Venkat Narayana H. Sudarshan B.A. Daniel T.S. Nayar R. Sukumar Ranjit Daniels Rohan Pethiyagoda R. Vasudeva Soubadra Devy Narendra Prasad K. Vasudevan P. Dharma Rajan M.K. Prasad Muthu Velautham P.S. Easa Asad Rahmani Arun Venkatraman Madhav Gadgil S.N. Rai Siddharth Yadav T. Ganesh Pratim Roy Santosh George P.S. -
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. -
Spermatogenesis and Histology of the Testes of the Caecilian, <Em
University of Richmond UR Scholarship Repository Biology Faculty Publications Biology 12-1986 Spermatogenesis and Histology of the Testes of the Caecilian, Chthonerpeton indistinctum Rafael O. de Sá University of Richmond, [email protected] Nibia Berois Follow this and additional works at: http://scholarship.richmond.edu/biology-faculty-publications Part of the Biology Commons, Developmental Biology Commons, and the Structural Biology Commons Recommended Citation Sá, Rafael de, and Nibia Berois. "Spermatogenesis and Histology of the Testes of the Caecilian, Chthonerpeton indistinctum." Journal of Herpetology 20, no. 4 (December 1986): 510-14. doi:10.2307/1564247. This Article is brought to you for free and open access by the Biology at UR Scholarship Repository. It has been accepted for inclusion in Biology Faculty Publications by an authorized administrator of UR Scholarship Repository. For more information, please contact [email protected]. fourn•I of Herpetology, Vol. 20, No. 4, pp. 510-514, 1986 Copyright 1986 Society for the Study of Amphibians and Reptiles Spermatogenesis and Histology of the Testes of the Caecilian, Chthonerpeton indistinctum RAFAEL DE SA1 AND NIBIA BEROIS2 1Museum of Natural History and Department of Systematics and Ecology, The University of Kansas, Lawrence, Kansas 66045-2454, USA 2Departamento de Biologfa Celular, Facultad de Humanidades y Ciencias, Universidad Mayor de la Republica Oriental del Uruguay, Tristan Narvaja 1674, Montevideo, Uruguay ABSTRACT. - Macroscopically, the testes of Chthonerpeton indistinctum consist of a series of oval lobes. The number and size of lobes is variable in Chthonerpeton indistinctum. Histologically, the testes are divided into structural units, locules separated by septa of connective tissue. Inside of each locule spermatogenesis takes place in cysts of germinal cells that divide synchronically. -
Gymnophiona: Caeciliidae) from the Techniques, and Recent Predictions Western Ghats of Goa and Karnataka (Dinesh Et Al
JoTT NOTE 2(8): 1105-1108 New site records of Gegeneophis upsurge in the description of new goaensis and G. mhadeiensis species in Gegeneophis may be due to optimization of surveying (Gymnophiona: Caeciliidae) from the techniques, and recent predictions Western Ghats of Goa and Karnataka (Dinesh et al. 2009) indicate future discovery of new species from this genus. 1 2 Gopalakrishna Bhatta , K.P. Dinesh , Gegeneophis goaensis was described by Bhatta et 3 4 P. Prashanth , Nirmal U. Kulkarni & al. (2007a) from Keri Village, Sattari Taluk, North Goa 5 C. Radhakrishnan District, Goa based on a set of three specimens collected in September 2006 and July 2008. G. mhadeiensis 1 Department of Biology, BASE Educational Service Pvt. Ltd., was described in 2007 from Chorla Village, Khanapur Basavanagudi, Bengaluru, Karnataka 560004, India 2,5 Zoological Survey of India, Western Ghat Regional Centre, Taluk, Belgaum District, Karnataka from a set of three Eranhipalam, Kozhikode, Kerala 673006, India specimens collected during 2006 (Bhatta et al. 2007b). 3 Agumbe Rainforest Research Station, Agumbe, Karnataka During our recent explorations for these secretive animals 577411, India 4 in the bordering districts of Maharashtra (Sindhudurg), Hiru Naik Building, Dhuler Mapusa, Goa 403507, India Email: 2 [email protected] (corresponding author) Goa (North Goa) and Karnataka (Belgaum), we collected an individual of G. goaensis (Image 1) below the soil heap surrounding a banana plantation in Chorla In India the order Gymnophiona Müller is represented Village (Karnataka) on 05 August 2009 (Table 1). All by 26 species under four genera in two families (Dinesh the morphological and morphometric details were in et al. -
Biogeographic Analysis Reveals Ancient Continental Vicariance and Recent Oceanic Dispersal in Amphibians ∗ R
Syst. Biol. 63(5):779–797, 2014 © The Author(s) 2014. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. All rights reserved. For Permissions, please email: [email protected] DOI:10.1093/sysbio/syu042 Advance Access publication June 19, 2014 Biogeographic Analysis Reveals Ancient Continental Vicariance and Recent Oceanic Dispersal in Amphibians ∗ R. ALEXANDER PYRON Department of Biological Sciences, The George Washington University, 2023 G Street NW, Washington, DC 20052, USA; ∗ Correspondence to be sent to: Department of Biological Sciences, The George Washington University, 2023 G Street NW, Washington, DC 20052, USA; E-mail: [email protected]. Received 13 February 2014; reviews returned 17 April 2014; accepted 13 June 2014 Downloaded from Associate Editor: Adrian Paterson Abstract.—Amphibia comprises over 7000 extant species distributed in almost every ecosystem on every continent except Antarctica. Most species also show high specificity for particular habitats, biomes, or climatic niches, seemingly rendering long-distance dispersal unlikely. Indeed, many lineages still seem to show the signature of their Pangaean origin, approximately 300 Ma later. To date, no study has attempted a large-scale historical-biogeographic analysis of the group to understand the distribution of extant lineages. Here, I use an updated chronogram containing 3309 species (~45% of http://sysbio.oxfordjournals.org/ extant diversity) to reconstruct their movement between 12 global ecoregions. I find that Pangaean origin and subsequent Laurasian and Gondwanan fragmentation explain a large proportion of patterns in the distribution of extant species. However, dispersal during the Cenozoic, likely across land bridges or short distances across oceans, has also exerted a strong influence.