Petition to Add Bullfrogs to List of Restricted Species
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The Origins of Chordate Larvae Donald I Williamson* Marine Biology, University of Liverpool, Liverpool L69 7ZB, United Kingdom
lopmen ve ta e l B Williamson, Cell Dev Biol 2012, 1:1 D io & l l o l g DOI: 10.4172/2168-9296.1000101 e y C Cell & Developmental Biology ISSN: 2168-9296 Research Article Open Access The Origins of Chordate Larvae Donald I Williamson* Marine Biology, University of Liverpool, Liverpool L69 7ZB, United Kingdom Abstract The larval transfer hypothesis states that larvae originated as adults in other taxa and their genomes were transferred by hybridization. It contests the view that larvae and corresponding adults evolved from common ancestors. The present paper reviews the life histories of chordates, and it interprets them in terms of the larval transfer hypothesis. It is the first paper to apply the hypothesis to craniates. I claim that the larvae of tunicates were acquired from adult larvaceans, the larvae of lampreys from adult cephalochordates, the larvae of lungfishes from adult craniate tadpoles, and the larvae of ray-finned fishes from other ray-finned fishes in different families. The occurrence of larvae in some fishes and their absence in others is correlated with reproductive behavior. Adult amphibians evolved from adult fishes, but larval amphibians did not evolve from either adult or larval fishes. I submit that [1] early amphibians had no larvae and that several families of urodeles and one subfamily of anurans have retained direct development, [2] the tadpole larvae of anurans and urodeles were acquired separately from different Mesozoic adult tadpoles, and [3] the post-tadpole larvae of salamanders were acquired from adults of other urodeles. Reptiles, birds and mammals probably evolved from amphibians that never acquired larvae. -
Progress Report for the San Joaquin Valley Giant Garter Snake
PROGRESS REPORT: 2003 SAN JOAQUIN VALLEY GIANT GARTER SNAKE CONSERVATION PROJECT Prepared by: Todd Williams, Wildlife Biologist Veronica Wunderlich, Biological Science Technician U.S. Fish & Wildlife Service San Luis National Wildlife Refuge Complex Box 2176 Los Banos, CA 93635 INTRODUCTION & BACKGROUND: The giant garter snake, Thamnophis gigas (Rossman & Stewart 1987), was designated as a federally threatened species throughout its range in October 1993 and (USFWS 1993). Giant garter snakes are endemic to the Central Valley of California, and historically occurred throughout the San Joaquin and Sacramento Valleys (Hansen and Brode 1980). They are thought to have occurred as far north as Butte County and south to Kern County, within the boundaries of the foothills of the Coastal and Sierra Nevada ranges. The current range of the giant garter snake is confined to the Sacramento Valley and isolated portions of the San Joaquin Valley (USFWS 1999). The giant garter snake is primarily an aquatic species that feeds on small fishes, tadpoles, and frogs (Fitch 1941). Historically, prey items included thick-tailed chub (Gila crassicauda), Sacramento blackfish (Orthodox microlepidus), and the California red- legged frog (Rana aurora draytoni), all of which have been extirpated from the giant garter snake’s current range (Rossman et al 1996). The habitat requirements of giant garter snakes include wetland areas with sufficient emergent vegetation for cover, openings in the vegetation for basking, and access to rodent burrows for shelter and winter periods of reduced activity (USFWS 1993). Giant garter snakes tend to be absent from rivers that support populations of large predatory fish as well as watercourses that have sand, gravel or rocky substrates (Hansen 1980). -
Biology and Impacts of Pacific Island Invasive Species. 8
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln USDA National Wildlife Research Center - Staff U.S. Department of Agriculture: Animal and Publications Plant Health Inspection Service 2012 Biology and Impacts of Pacific Island Invasive Species. 8. Eleutherodactylus planirostris, the Greenhouse Frog (Anura: Eleutherodactylidae) Christina A. Olson Utah State University, [email protected] Karen H. Beard Utah State University, [email protected] William C. Pitt National Wildlife Research Center, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/icwdm_usdanwrc Olson, Christina A.; Beard, Karen H.; and Pitt, William C., "Biology and Impacts of Pacific Island Invasive Species. 8. Eleutherodactylus planirostris, the Greenhouse Frog (Anura: Eleutherodactylidae)" (2012). USDA National Wildlife Research Center - Staff Publications. 1174. https://digitalcommons.unl.edu/icwdm_usdanwrc/1174 This Article is brought to you for free and open access by the U.S. Department of Agriculture: Animal and Plant Health Inspection Service at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in USDA National Wildlife Research Center - Staff Publications by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Biology and Impacts of Pacific Island Invasive Species. 8. Eleutherodactylus planirostris, the Greenhouse Frog (Anura: Eleutherodactylidae)1 Christina A. Olson,2 Karen H. Beard,2,4 and William C. Pitt 3 Abstract: The greenhouse frog, Eleutherodactylus planirostris, is a direct- developing (i.e., no aquatic stage) frog native to Cuba and the Bahamas. It was introduced to Hawai‘i via nursery plants in the early 1990s and then subsequently from Hawai‘i to Guam in 2003. The greenhouse frog is now widespread on five Hawaiian Islands and Guam. -
Amphibia: Anura: Eleutherodactylidae), from Eastern Cuba
124 SOLENODON 12: 124-135, 2015 Another new cryptic frog related to Eleutherodactylus varleyi Dunn (Amphibia: Anura: Eleutherodactylidae), from eastern Cuba Luis M. DÍAZ* and S. Blair HEDGES** *Museo Nacional de Historia Natural de Cuba, Obispo #61, Esquina Oficios, Plaza de Armas, Habana Vieja, CP 10100, Cuba. [email protected] **Department of Biology, 208 Mueller Laboratory, Pennsylvania State University, University Park, Pennsylvania 16802-530, USA. [email protected] ABSTRacT. A new cryptic frog, Eleutherodactylus beguei sp. nov., is described from the pine forests of La Munición, Yateras, Guantánamo Province, Cuba. It is sympatric with E. feichtin- geri, another recently described grass frog closely related to E. varleyi, but differs in morphol- ogy, vocalization and DNA sequences of the mitochondrial Cyt-b gene. One female of the new species was found vocalizing in response to a calling male, a behavior that is still poorly documented in anurans. Same male and female were found in axillary amplexus and sur- rounded by 9 eggs (3.5–3.7 mm in diameter) 5 hours after being isolated in a small container. Key words: Amphibia, Anura, Eleutherodactylidae, Eleutherodactylus, new species, Terrarana, Euhyas, West Indies, Guantánamo, female reciprocation calls, eggs. INtrODUCtION After a recent review of the geographic variation of the Cuban Grass Frog Eleutherodactylus varleyi Dunn, Díaz et al. (2012) described E. feichtingeri, a cryptic species widely distributed in central and eastern Cuba. the two species differ primarily in tympanum size, supratympanic stripe pattern, and advertisement calls. Species recognition was also supported by genetic and cytogenetic data. One of the authors (SBH) conducted DNA sequence analyses that confirmed the existence of two species at La Munición, Humboldt National Park. -
Missouri's Toads and Frogs Booklet
TOADSMissouri’s andFROGS by Jeffrey T. Briggler and Tom R. Johnson, Herpetologists www.MissouriConservation.org © 1982, 2008 Missouri Conservation Commission Equal opportunity to participate in and benefit from programs of the Missouri Department of Conservation is available to all individuals without regard to their race, color, national origin, sex, age or disability. Questions should be directed to the Department of Conservation, P.O. Box 180, Jefferson City, MO 65102, (573) 751-4115 (voice) or 800-735-2966 (TTY), or to the U.S. Fish and Wildlife Service Division of Federal Assistance, 4401 N. Fairfax Drive, Mail Stop: MBSP-4020, Arlington, VA 22203. Cover photo: Eastern gray treefrog by Tom R. Johnson issouri toads and frogs are colorful, harmless, vocal and valuable. Our forests, prairies, rivers, swamps and marshes are Mhome to a multitude of toads and frogs, but few people know how many varieties we have, how to tell them apart, or much about their natural history. Studying these animals and sharing their stories with fellow Missourians is one of the most pleasurable and rewarding aspects of our work. Toads and frogs are amphibians—a class Like most of vertebrate animals that also includes amphibians, salamanders and the tropical caecilians, which are long, slender, wormlike and legless. frogs and Missouri has 26 species and subspecies (or toads have geographic races) of toads and frogs. Toads and frogs differ from salamanders by having an aquatic relatively short bodies and lacking tails at adulthood. Being an amphibian means that tadpole stage they live two lives: an aquatic larval or tadpole and a semi- stage and a semi-aquatic or terrestrial adult stage. -
This Article Appeared in a Journal Published by Elsevier. the Attached
(This is a sample cover image for this issue. The actual cover is not yet available at this time.) This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and education use, including for instruction at the authors institution and sharing with colleagues. Other uses, including reproduction and distribution, or selling or licensing copies, or posting to personal, institutional or third party websites are prohibited. In most cases authors are permitted to post their version of the article (e.g. in Word or Tex form) to their personal website or institutional repository. Authors requiring further information regarding Elsevier’s archiving and manuscript policies are encouraged to visit: http://www.elsevier.com/copyright Author's personal copy Toxicon 60 (2012) 967–981 Contents lists available at SciVerse ScienceDirect Toxicon journal homepage: www.elsevier.com/locate/toxicon Antimicrobial peptides and alytesin are co-secreted from the venom of the Midwife toad, Alytes maurus (Alytidae, Anura): Implications for the evolution of frog skin defensive secretions Enrico König a,*, Mei Zhou b, Lei Wang b, Tianbao Chen b, Olaf R.P. Bininda-Emonds a, Chris Shaw b a AG Systematik und Evolutionsbiologie, IBU – Fakultät V, Carl von Ossietzky Universität Oldenburg, Carl von Ossietzky Strasse 9-11, 26129 Oldenburg, Germany b Natural Drug Discovery Group, School of Pharmacy, Medical Biology Center, Queen’s University, 97 Lisburn Road, Belfast BT9 7BL, Northern Ireland, UK article info abstract Article history: The skin secretions of frogs and toads (Anura) have long been a known source of a vast Received 23 March 2012 abundance of bioactive substances. -
Giant Garter Snake: the Role of Rice and Effects of Water Transfers
Giant Garter Snake: The Role of Rice and Effects of Water Transfers Report of Point Blue Conservation Science May 2017 W. David Shuford Giant Garter Snake: The role of rice and effects of water transfers May 2017 Point Blue Conservation Science W. David Shuford Suggested Citation: Shuford, W. D. 2017. Giant Garter Snake: The role of rice and effects of water transfers. Report of Point Blue Conservation Science, 3820 Cypress Drive #11, Petaluma, CA 94954. Point Blue Contribution No. 2133. Point Blue Conservation Science – Point Blue’s 140 staff and seasonal scientists conserve birds, other wildlife and their ecosystems through scientific research and outreach. At the core of our work is ecosystem science, studying birds and other indicators of nature’s health. Visit Point Blue on the web www.pointblue.org. Main Points Effects on the federally and state threatened giant garter snake are a major concern under a long-term (10-year) plan to transfer water from sellers in the Sacramento Valley to users south of the Delta or in the San Francisco Bay Area. Water will be made available for transfer from cropland idling, crop shifting, groundwater substitution, reservoir release, and conservation. A maximum of 60,693 acres of rice land would be fallowed each year if the full amount of 565,614 acre feet of surface water is transferred annually. This level of idling potentially could have major impacts on this snake given the current importance of the rice landscape in the Sacramento Valley to the species’ continued survival. Giant garter snakes in the Sacramento Valley have a strong association with natural wetlands and aquatic agricultural habitats, particularly rice and associated water conveyances. -
Giant Garter Snake Habitat Quantification Tool
Giant Garter Snake Habitat Quantification Tool Part of the Multispecies Habitat Quantification Tool for the Central Valley Habitat Exchange Scientific Rationale and Methods Document, Version 5 Multispecies Habitat Quantification Tool: Giant Garter Snake Acknowledgements The development of the scientific approach for quantifying impacts and benefits to multiple species for use in the Central Valley Habitat Exchange (Exchange) would not have been possible without the input and guidance from a group of technical experts who worked to develop the contents of this tool. This included members of the following teams: Central Valley Habitat Exchange Project Coordinators John Cain (American Rivers) Daniel Kaiser (Environmental Defense Fund) Katie Riley (Environmental Incentives) Exchange Science Team Stefan Lorenzato (Department of Water Resources) Stacy Small-Lorenz (Environmental Defense Fund) Rene Henery (Trout Unlimited) Nat Seavy (Point Blue) Jacob Katz (CalTrout) Tool Developers Amy Merrill (Stillwater Sciences) Sara Gabrielson (Stillwater Sciences) Holly Burger (Stillwater Sciences) AJ Keith (Stillwater Sciences) Evan Patrick (Environmental Defense Fund) Kristen Boysen (Environmental Incentives) Giant Garter Snake TAC Brian Halstead (USGS) Laura Patterson (CDFW) Ron Melcer (formerly DWR; with Delta Stewardship Council as of February 2017) Chinook Salmon TAC Alison Collins (Metropolitan Water District) Brett Harvey (DWR) Brian Ellrott (NOAA/NMFS) Cesar Blanco (USFWS) Corey Phillis (Metropolitan Water District) Dave Vogel (Natural Resource -
High Abundance of Invasive African Clawed Frog Xenopus Laevis in Chile: Challenges for Their Control and Updated Invasive Distribution
Management of Biological Invasions (2019) Volume 10, Issue 2: 377–388 CORRECTED PROOF Research Article High abundance of invasive African clawed frog Xenopus laevis in Chile: challenges for their control and updated invasive distribution Marta Mora1, Daniel J. Pons2,3, Alexandra Peñafiel-Ricaurte2, Mario Alvarado-Rybak2, Saulo Lebuy2 and Claudio Soto-Azat2,* 1Vida Nativa NGO, Santiago, Chile 2Centro de Investigación para la Sustentabilidad & Programa de Doctorado en Medicina de la Conservación, Facultad de Ciencias de la Vida, Universidad Andres Bello, Republica 440, Santiago, Chile 3Facultad de Ciencias Exactas, Departamento de Matemáticas, Universidad Andres Bello, Santiago, Republica 470, Santiago, Chile Author e-mails: [email protected] (CSA), [email protected] (MM), [email protected] (DJP), [email protected] (APR), [email protected] (MAR), [email protected] (SL) *Corresponding author Citation: Mora M, Pons DJ, Peñafiel- Ricaurte A, Alvarado-Rybak M, Lebuy S, Abstract Soto-Azat C (2019) High abundance of invasive African clawed frog Xenopus Invasive African clawed frog Xenopus laevis (Daudin, 1802) are considered a major laevis in Chile: challenges for their control threat to aquatic environments. Beginning in the early 1970s, invasive populations and updated invasive distribution. have now been established throughout much of central Chile. Between September Management of Biological Invasions 10(2): and December 2015, we studied a population of X. laevis from a small pond in 377–388, https://doi.org/10.3391/mbi.2019. 10.2.11 Viña del Mar, where we estimated the population size and evaluated the use of hand nets as a method of control. First, by means of a non-linear extrapolation Received: 26 October 2018 model using the data from a single capture session of 200 min, a population size of Accepted: 7 March 2019 1,182 post-metamorphic frogs (range: 1,168–1,195 [quadratic error]) and a density Published: 16 May 2019 of 13.7 frogs/m2 (range: 13.6–13.9) of surface water were estimated. -
Biology and Impacts of Pacific Island Invasive Species. 5. Eleutherodactylus Coqui, the Coqui Frog
Biology and Impacts of Pacific Island Invasive Species. 5. Eleutherodactylus coqui, the Coqui Frog (Anura: Leptodactylidae)1 Karen H. Beard,2,5 Emily A. Price,3 and William C. Pitt4 Abstract: The nocturnal, terrestrial frog Eleutherodactylus coqui, known as the Coqui, is endemic to Puerto Rico and was accidentally introduced to Hawai‘i via nursery plants in the late 1980s. Over the past two decades E. coqui has spread to the four main Hawaiian Islands, and a major campaign was launched to eliminate and control it. One of the primary reasons this frog has received attention is its loud mating call (85–90 dB at 0.5 m). Many homeowners do not want the frogs on their property, and their presence has influenced housing prices. In addition, E. coqui has indirectly impacted the floriculture industry be- cause customers are reticent to purchase products potentially infested with frogs. Eleutherodactylus coqui attains extremely high densities in Hawai‘i, up to 91,000 frogs haÀ1, and can reproduce year-round, once every 1–2 months, and become reproductive around 8–9 months. Although the Coqui has been hy- pothesized to potentially compete with native insectivores, the most obvious po- tential ecological impact of the invasion is predation on invertebrate populations and disruption of associated ecosystem processes. Multiple forms of control have been attempted in Hawai‘i with varying success. The most successful con- trol available at this time is citric acid. Currently, the frog is established throughout the island of Hawai‘i but may soon be eliminated on the other Ha- waiian Islands via control efforts. -
Pre-Incursion Plan PIP003 Toads and Frogs
Pre-incursion Plan PIP003 Toads and Frogs Scope This plan is in place to guide prevention and eradication activities and the management of non-indigenous populations of Toads and Frogs (Order Anura) in the wild in Victoria. Version Document Status Date Author Reviewed By Approved for Release 1.0 First Draft 26/07/11 Dana Price M. Corry, S. Wisniewski and A. Woolnough 1.1 Second Draft 21/10/11 Dana Price S. Wisniewski 2.0 Final Draft 11/01/12 Dana Price S.Wisniewski 2.1 Final 27/06/12 Dana Price M.Corry Visual Standard approved by ADP 3.0 New Final 6/10/15 Dana Price A.Kay New DEDJTR template and document revision Acknowledgement and special thanks to Peter Courtenay, Senior Curator, Zoos Victoria, for reviewing this document and providing comments. Published by the Department of Economic Development, Jobs, Transport and Resources, Agriculture Victoria, May 2016 © The State of Victoria 2016. This publication is copyright. No part may be reproduced by any process except in accordance with the provisions of the Copyright Act 1968. Authorised by the Department of Economic Development, Jobs, Transport and Resources, 1 Spring Street, Melbourne 3000. Front cover: Cane Toad (Rhinella marinus) Photo: Image courtesy of Ryan Melville, HRIA Team, DEDJTR For more information about Agriculture Victoria go to www.agriculture.vic.gov.au or phone the Customer Service Centre on 136 186. ISBN 978-1-925532-37-1 (pdf/online) Disclaimer This publication may be of assistance to you but the State of Victoria and its employees do not guarantee that the publication is without flaw of any kind or is wholly appropriate for your particular purposes and therefore disclaims all liability for any error, loss or other consequence which may arise from you relying on any information in this publication. -
Geographic Distribution, Colour Variation and Molecular Diversity of Miniature Frogs of the Eleutherodactylus Limbatus Group from Cuba
SALAMANDRA 48(2) 71–91 30 June Diversity2012 ISSNof miniature 0036–3375 frogs from Cuba Geographic distribution, colour variation and molecular diversity of miniature frogs of the Eleutherodactylus limbatus group from Cuba Ariel Rodríguez 1, Roberto Alonso 2, José Antonio Rodríguez 3 & Miguel Vences 4 1) Instituto de Ecología y Sistemática, Carr. de Varona, Km 3½, Capdevila, Boyeros, AP 8029, CP 10800, La Habana, Cuba 2) Museo de Historia Natural ‘Felipe Poey’, Facultad de Biología, Universidad de La Habana, La Habana, Cuba 3) Unidad de Servicios Ambientales PN Alejandro de Humboldt, Sector Baracoa, Guantánamo, Cuba 4) Zoologisches Institut, Technische Universität Braunschweig, Mendelssohnstr. 4, 38106 Braunschweig, Germany Corresponding author: Ariel Rodríguez, e-mail: [email protected] Manuscript received: 20 January 2012 Abstract. The endemic Cuban Eleutherodactylus limbatus group contains five species of miniature species of frogs E. cu( banus, E. iberia, E. jaumei, E. limbatus, E. orientalis), and one larger and more generalized species (E. etheridgei). Several of the miniature species have contrasting colour patterns with bright yellow or white stripes on a dark dorsum, and two of these species are known to sequester skin alkaloids. Based on a review of literature, museum data and numerous own, unpublished field records we provide an updated list of georeferenced locality records of all species of the group that con- firms their strict allopatric distribution pattern despite the close geographic proximity of some species. A phylogenetic tree based on newly analysed partial DNA sequences of the mitochondrial cytochrome b gene (566 bp) placed the dull- coloured species E. etheridgei and E. cubanus in a basal position, followed by a well-differentiatedE.