Type-Specimens of Amphibians in the University of Michigan Museum of Zoology
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Kemp's Ridley Sea Turtle Headstart 08/1994 Program (NOAA Tech Memo NMFS-OPR-3) TED Regulations for Shrimp Trawls 57 FR 57348 12/04/1992 Recovery Plan - U.S
Fishing Permits Habitat Conservation Grants Fisheries Environmental Analyses Endangered Spec Search Go fish! nmlkji This si nmlkj All of NMFS Home Threatened and Endangered Species Divisions/Branches Lists What We Do Fishery Bulletins The following list of species under NMFS Fishery Quotas jurisdiction, listed as threatened or endangered, Fishery Regulations for each state and territory. Click on the state, News/Media territory or areas below to view a list of Species: National Employee 1. Southeast Region (North Carolina to Texas and Locator the Caribbean) FOIA Information 2. South Atlantic (North Carolina to Key West Public Records Florida) Request 3. Gulf of Mexico 4. Alabama 5. Florida - Atlantic Coast 6. Florida - Gulf Coast 7. Georgia 8. Louisiana 9. Mississippi 10. North Carolina 11. Puerto Rico 12. South Carolina 13. Texas 14. U.S. Virgin Islands Home · Privacy Policy · Disclaimer · About Us · Information Quality · Contact Us · Last Updated: February 2, 2010 NOAA Fisheries Office of Protected Resources OPR Home | About OPR | Species | Permits | Laws & Policies | Programs | Education | Publications Loggerhead Turtle (Caretta caretta) Species Marine Mammals Status | Taxonomy | Species Description | Habitat | Distribution | Cetaceans Population Trends | Threats | Conservation Efforts | Regulatory Overview | Pinnipeds Key Documents | More Info Marine Turtles Marine & Anadromous Fish Status Marine Invertebrates & ESA Threatened - throughout its range Plants Species of Concern Taxonomy Threatened & Endangered Kingdom: Animalia Species Phylum: Chordata Critical Habitat Maps Class: Reptilia Order: Testudines Loggerhead turtle hatchling (Caretta caretta) Family: Cheloniidae Contact OPR Photo: Mary Wozny, Broward Glossary Genus: Caretta County Florida Sea Turtle OPR Site Map Species: caretta Conservation Program Species Description Did You Know? Loggerheads were named for their relatively large heads, which support powerful jaws and enable them to feed on Search OPR hard-shelled prey, such as whelks and conch. -
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. -
Anura, Rhacophoridae)
Zoologica Scripta Patterns of reproductive-mode evolution in Old World tree frogs (Anura, Rhacophoridae) MADHAVA MEEGASKUMBURA,GAYANI SENEVIRATHNE,S.D.BIJU,SONALI GARG,SUYAMA MEEGASKUMBURA,ROHAN PETHIYAGODA,JAMES HANKEN &CHRISTOPHER J. SCHNEIDER Submitted: 3 December 2014 Meegaskumbura, M., Senevirathne, G., Biju, S. D., Garg, S., Meegaskumbura, S., Pethiya- Accepted: 7 May 2015 goda, R., Hanken, J., Schneider, C. J. (2015). Patterns of reproductive-mode evolution in doi:10.1111/zsc.12121 Old World tree frogs (Anura, Rhacophoridae). —Zoologica Scripta, 00, 000–000. The Old World tree frogs (Anura: Rhacophoridae), with 387 species, display a remarkable diversity of reproductive modes – aquatic breeding, terrestrial gel nesting, terrestrial foam nesting and terrestrial direct development. The evolution of these modes has until now remained poorly studied in the context of recent phylogenies for the clade. Here, we use newly obtained DNA sequences from three nuclear and two mitochondrial gene fragments, together with previously published sequence data, to generate a well-resolved phylogeny from which we determine major patterns of reproductive-mode evolution. We show that basal rhacophorids have fully aquatic eggs and larvae. Bayesian ancestral-state reconstruc- tions suggest that terrestrial gel-encapsulated eggs, with early stages of larval development completed within the egg outside of water, are an intermediate stage in the evolution of ter- restrial direct development and foam nesting. The ancestral forms of almost all currently recognized genera (except the fully aquatic basal forms) have a high likelihood of being ter- restrial gel nesters. Direct development and foam nesting each appear to have evolved at least twice within Rhacophoridae, suggesting that reproductive modes are labile and may arise multiple times independently. -
Character Assessment, Genus Level Boundaries, and Phylogenetic Analyses of the Family Rhacophoridae: a Review and Present Day Status
Contemporary Herpetology ISSN 1094-2246 2000 Number 2 7 April 2000 CHARACTER ASSESSMENT, GENUS LEVEL BOUNDARIES, AND PHYLOGENETIC ANALYSES OF THE FAMILY RHACOPHORIDAE: A REVIEW AND PRESENT DAY STATUS Jeffery A. Wilkinson ([email protected]) and Robert C. Drewes ([email protected]) Department of Herpetology, California Academy of Sciences, Golden Gate Park, San Francisco, California 94118 Abstract. The first comprehensive phylogenetic analysis of the family Rhacophoridae was conducted by Liem (1970) scoring 81 species for 36 morphological characters. Channing (1989), in a reanalysis of Liem’s study, produced a phylogenetic hypothesis different from that of Liem. We compared the two studies and produced a third phylogenetic hypothesis based on the same characters. We also present the synapomorphic characters from Liem that define the major clades and each genus within the family. Finally, we summarize intergeneric relationships within the family as hypothesized by other studies, and the family’s current status as it relates to other ranoid families. The family Rhacophoridae is comprised of over 200 species of Asian and African tree frogs that have been categorized into 10 genera and two subfamilies (Buergerinae and Rhacophorinae; Duellman, 1993). Buergerinae is a monotypic category that accommodates the relatively small genus Buergeria. The remaining genera, Aglyptodactylus, Boophis, Chirixalus, Chiromantis, Nyctixalus, Philautus, Polyp edates, Rhacophorus, and Theloderma, comprise Rhacophorinae (Channing, 1989). The family is part of the neobatrachian clade Ranoidea, which also includes the families Ranidae, Hyperoliidae, Dendrobatidae, Arthroleptidae, the genus Hemisus, and possibly the family Microhylidae. The Ranoidea clade is distinguished from other neobatrachians by the synapomorphic characters of completely fused epicoracoid cartilages, the medial end of the coracoid being wider than the lateral end, and the insertion of the semitendinosus tendon being dorsal to the m. -
Molecular Phylogenetics and Evolution 123 (2018) 59–72
Molecular Phylogenetics and Evolution 123 (2018) 59–72 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Phylogenetic relationships and cryptic species diversity in the Brazilian egg- T brooding tree frog, genus Fritziana Mello-Leitão 1937 (Anura: Hemiphractidae) ⁎ Marina Walker1, , Mariana L. Lyra1, Célio F.B. Haddad Universidade Estadual Paulista, Instituto de Biociências, Departamento de Zoologia and Centro de Aquicultura (CAUNESP), Campus Rio Claro, Av. 24A,No 1515, Bela Vista, CEP 13506-900 Rio Claro, São Paulo, Brazil ARTICLE INFO ABSTRACT Keywords: The genus Fritziana (Anura: Hemiphractidae) comprises six described species (F. goeldii, F. ohausi, F. fissilis, F. Egg-brooding frogs ulei, F. tonimi, and F. izecksohni) that are endemic to the Brazilian Atlantic Forest. Although the genus has been Molecular phylogeny the subject of studies dealing with its taxonomy, phylogeny, and systematics, there is considerable evidence for Brazilian Atlantic Forest cryptic diversity hidden among the species. The present study aims to understand the genetic diversity and Species diversity phylogenetic relationships among the species of Fritziana, as well as the relationships among populations within New candidate species species. We analyzed 107 individuals throughout the distribution of the genus using three mitochondrial gene Mitochondrial gene rearrangements fragments (12S, 16S, and COI) and two nuclear genes (RAG1 and SLC8A3). Our data indicated that the species diversity in the genus Fritziana is underestimated by the existence of at least three candidate species hidden amongst the group of species with a closed dorsal pouch (i.e. F. fissilis and F. ulei). We also found four species presenting geographical population structures and high genetic diversity, and thus require further investigations. -
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. -
Biology Assessment Plan Spring 2019
Biological Sciences Department 1 Biology Assessment Plan Spring 2019 Task: Revise the Biology Program Assessment plans with the goal of developing a sustainable continuous improvement plan. In order to revise the program assessment plan, we have been asked by the university assessment committee to revise our Students Learning Outcomes (SLOs) and Program Learning Outcomes (PLOs). Proposed revisions Approach: A large community of biology educators have converged on a set of core biological concepts with five core concepts that all biology majors should master by graduation, namely 1) evolution; 2) structure and function; 3) information flow, exchange, and storage; 4) pathways and transformations of energy and matter; and (5) systems (Vision and Change, AAAS, 2011). Aligning our student learning and program goals with Vision and Change (V&C) provides many advantages. For example, the V&C community has recently published a programmatic assessment to measure student understanding of vision and change core concepts across general biology programs (Couch et al. 2019). They have also carefully outlined student learning conceptual elements (see Appendix A). Using the proposed assessment will allow us to compare our student learning profiles to those of similar institutions across the country. Revised Student Learning Objectives SLO 1. Students will demonstrate an understanding of core concepts spanning scales from molecules to ecosystems, by analyzing biological scenarios and data from scientific studies. Students will correctly identify and explain the core biological concepts involved relative to: biological evolution, structure and function, information flow, exchange, and storage, the pathways and transformations of energy and matter, and biological systems. More detailed statements of the conceptual elements students need to master are presented in appendix A. -
Extreme Morphological and Ecological Homoplasy in Tropical Salamanders
Extreme morphological and ecological homoplasy in tropical salamanders Gabriela Parra-Olea* and David B. Wake† Museum of Vertebrate Zoology and Department of Integrative Biology, University of California, Berkeley, CA 94720-3160 Contributed by David B. Wake, April 25, 2001 Fossorial salamanders typically have elongate and attenuated We analyzed sequences of mtDNA of many tropical bolito- heads and bodies, diminutive limbs, hands and feet, and extremely glossines, including all recognized genera, and determined that elongate tails. Batrachoseps from California, Lineatriton from east- Lineatriton and Oedipina are much more closely related to other ern Me´xico, and Oedipina from southern Me´xico to Ecuador, all taxa than to each other (3, 4). Not only was Lineatriton deeply members of the family Plethodontidae, tribe Bolitoglossini, resem- nested within the large, mainly Mexican genus Pseudoeurycea, ble one another in external morphology, which has evolved inde- but populations of Lineatriton from different parts of its geo- pendently. Whereas Oedipina and Batrachoseps are elongate be- graphic range were more closely related to different species of cause there are more trunk vertebrae, a widespread homoplasy Pseudoeurycea than to each other. Here we analyze molecular (parallelism) in salamanders, the genus Lineatriton is unique in data for 1,816 bp of mtDNA derived from three genes, reject the having evolved convergently by an alternate ‘‘giraffe-neck’’ de- monophyly of Lineatriton, and support an extraordinary case of velopmental program. Lineatriton has the same number of trunk homoplasy in a putative species that previously has been con- vertebrae as related, nonelongated taxa, but individual trunk sidered to be extremely specialized, and unique, in both mor- vertebrae are elongated. -
Comparative Osteology and Evolution of the Lungless Salamanders, Family Plethodontidae David B
COMPARATIVE OSTEOLOGY AND EVOLUTION OF THE LUNGLESS SALAMANDERS, FAMILY PLETHODONTIDAE DAVID B. WAKE1 ABSTRACT: Lungless salamanders of the family Plethodontidae comprise the largest and most diverse group of tailed amphibians. An evolutionary morphological approach has been employed to elucidate evolutionary rela tionships, patterns and trends within the family. Comparative osteology has been emphasized and skeletons of all twenty-three genera and three-fourths of the one hundred eighty-three species have been studied. A detailed osteological analysis includes consideration of the evolution of each element as well as the functional unit of which it is a part. Functional and developmental aspects are stressed. A new classification is suggested, based on osteological and other char acters. The subfamily Desmognathinae includes the genera Desmognathus, Leurognathus, and Phaeognathus. Members of the subfamily Plethodontinae are placed in three tribes. The tribe Hemidactyliini includes the genera Gyri nophilus, Pseudotriton, Stereochilus, Eurycea, Typhlomolge, and Hemidac tylium. The genera Plethodon, Aneides, and Ensatina comprise the tribe Pleth odontini. The highly diversified tribe Bolitoglossini includes three super genera. The supergenera Hydromantes and Batrachoseps include the nominal genera only. The supergenus Bolitoglossa includes Bolitoglossa, Oedipina, Pseudoeurycea, Chiropterotriton, Parvimolge, Lineatriton, and Thorius. Manculus is considered to be congeneric with Eurycea, and Magnadig ita is congeneric with Bolitoglossa. Two species are assigned to Typhlomolge, which is recognized as a genus distinct from Eurycea. No. new information is available concerning Haptoglossa. Recognition of a family Desmognathidae is rejected. All genera are defined and suprageneric groupings are defined and char acterized. Range maps are presented for all genera. Relationships of all genera are discussed. -
Bibliography and Scientific Name Index to Amphibians
lb BIBLIOGRAPHY AND SCIENTIFIC NAME INDEX TO AMPHIBIANS AND REPTILES IN THE PUBLICATIONS OF THE BIOLOGICAL SOCIETY OF WASHINGTON BULLETIN 1-8, 1918-1988 AND PROCEEDINGS 1-100, 1882-1987 fi pp ERNEST A. LINER Houma, Louisiana SMITHSONIAN HERPETOLOGICAL INFORMATION SERVICE NO. 92 1992 SMITHSONIAN HERPETOLOGICAL INFORMATION SERVICE The SHIS series publishes and distributes translations, bibliographies, indices, and similar items judged useful to individuals interested in the biology of amphibians and reptiles, but unlikely to be published in the normal technical journals. Single copies are distributed free to interested individuals. Libraries, herpetological associations, and research laboratories are invited to exchange their publications with the Division of Amphibians and Reptiles. We wish to encourage individuals to share their bibliographies, translations, etc. with other herpetologists through the SHIS series. If you have such items please contact George Zug for instructions on preparation and submission. Contributors receive 50 free copies. Please address all requests for copies and inquiries to George Zug, Division of Amphibians and Reptiles, National Museum of Natural History, Smithsonian Institution, Washington DC 20560 USA. Please include a self-addressed mailing label with requests. INTRODUCTION The present alphabetical listing by author (s) covers all papers bearing on herpetology that have appeared in Volume 1-100, 1882-1987, of the Proceedings of the Biological Society of Washington and the four numbers of the Bulletin series concerning reference to amphibians and reptiles. From Volume 1 through 82 (in part) , the articles were issued as separates with only the volume number, page numbers and year printed on each. Articles in Volume 82 (in part) through 89 were issued with volume number, article number, page numbers and year. -
New Sahonagasy Action Plan 2016-2020
New Sahonagasy Action Plan 2016-2020 1 New Sahonagasy Action Plan 2016 – 2020 Nouveau plan d’Action Sahonagasy 2016 – 2020 Edited by: Franco Andreone, IUCN SSC Amphibian Specialist Group - Madagascar Jeff S. Dawson, Durrell Wildlife Conservation Trust Falitiana C. E. Rabemananjara, IUCN SSC Amphibian Specialist Group - Madagascar Nirhy H.C. Rabibisoa, IUCN SSC Amphibian Specialist Group - Madagascar Tsanta F. Rakotonanahary, Durrell Wildlife Conservation Trust With assistance from: Candace M. Hansen-Hendrikx, Amphibian Survival Alliance James P. Lewis, Amphibian Survival Alliance/Rainforest Trust Published by: Museo Regionale di Scienze Naturali (Turin, Italy) and Amphibian Survival Alliance (Warrenton, VA) Publication date: June 2016 Recommended citation: Andreone, F., Dawson, J.S., Rabemananjara, F.C.E., Rabibisoa, N.H.C. & Rakotonanahary, T.F. (eds). 2016. New Sahonagasy Action Plan 2016–2020 / Nouveau Plan d'Action Sahonagasy 2016–2020. Museo Regionale di Scienze Naturali and Amphibian Survival Alliance, Turin. ISBN: 978-88-97189-26-8 Layout by: Candace M. Hansen-Hendrikx, Amphibian Survival Alliance Translation into French: Mathilde Malas, Speech Bubbles, www.speechbubbles.eu Printed by: Centro Stampa Regione Piemonte, Turin Front cover: Spinomantis aglavei, Gonçalo M. Rosa Back cover: Mantella expectata, Gonçalo M. Rosa IUCN - International Union for Conservation of Nature Founded in 1948, The International Union for Conservation of Nature brings together States, government agencies and a diverse range of nongovernmental organizations in a unique world partnership: over 1,000 members in all spread across some 140 countries. As a Union, IUCN seeks to influence, encourage and assist societies throughout the world to conserve the integrity and diversity of nature and to ensure that any use of natural resources is equitable and ecologically sustainable. -
Capítulo 4. Biodiversidad
Biodiversidad El cambio climático global y la pérdida de la biodiversidad son dos de los problemas ambientales más importantes que enfrenta la humanidad hoy día. La expansión e intensificación de las actividades humanas desde mediados del siglo pasado han cambiado radicalmente el funcionamiento en muchos ecosistemas en diversas regiones del mundo e, incluso, han alterado los patrones de biodiversidad a nivel local y regional. En algunos casos, estos cambios han provocado la extinción de muchas especies. Estimaciones sugieren que la tasa actual de extinción de especies a nivel mundial podría ser entre 10 y 1 000 veces mayor a la registrada con anterioridad a la presencia humana (Pimm et al., 1995). No obstante, los grandes esfuerzos que se han hecho en las últimas dos décadas a nivel internacional para conservar y utilizar sustentablemente la biodiversidad, han sido insuficientes para avanzar hacia el cumplimiento de las Metas de Aichi para la Diversidad Biológica (SCBD, 2014). De no haber cambios importantes, los pronósticos basados en la proyección de las tendencias actuales de los factores de presión más importantes, sugieren que la pérdida de la riqueza biológica global podría continuar cuando menos hasta el año 2020 (SCDB, 2010). Los efectos de la pérdida de la biodiversidad no se restringen al aspecto ambiental. Es ampliamente reconocido que el bienestar social y el desarrollo económico de las naciones, y en particular el de los países en desarrollo y el de las comunidades más vulnerables, están fincados en la continuidad de los servicios ambientales que brindan los ecosistemas y su biodiversidad (MEA, 2005). Para muchos países, incluido México, la pérdida de biodiversidad cobra mayor relevancia debido a que es considerado como uno de los centros de diversidad biológica más importantes del planeta, de hecho, forma parte del grupo de los 15 países megadiversos que concentran en conjunto entre el 60 y 70% de la biodiversidad global (Mittermeier et al., 1997; UNEP 2010).