D. Bruce Means
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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. -
Notophthalmus Perstriatus) Version 1.0
Species Status Assessment for the Striped Newt (Notophthalmus perstriatus) Version 1.0 Striped newt eft. Photo credit Ryan Means (used with permission). May 2018 U.S. Fish and Wildlife Service Region 4 Jacksonville, Florida 1 Acknowledgements This document was prepared by the U.S. Fish and Wildlife Service’s North Florida Field Office with assistance from the Georgia Field Office, and the striped newt Species Status Assessment Team (Sabrina West (USFWS-Region 8), Kaye London (USFWS-Region 4) Christopher Coppola (USFWS-Region 4), and Lourdes Mena (USFWS-Region 4)). Additionally, valuable peer reviews of a draft of this document were provided by Lora Smith (Jones Ecological Research Center) , Dirk Stevenson (Altamaha Consulting), Dr. Eric Hoffman (University of Central Florida), Dr. Susan Walls (USGS), and other partners, including members of the Striped Newt Working Group. We appreciate their comments, which resulted in a more robust status assessment and final report. EXECUTIVE SUMMARY This Species Status Assessment (SSA) is an in-depth review of the striped newt's (Notophthalmus perstriatus) biology and threats, an evaluation of its biological status, and an assessment of the resources and conditions needed to maintain species viability. We begin the SSA with an understanding of the species’ unique life history, and from that we evaluate the biological requirements of individuals, populations, and species using the principles of population resiliency, species redundancy, and species representation. All three concepts (or analogous ones) apply at both the population and species levels, and are explained that way below for simplicity and clarity as we introduce them. The striped newt is a small salamander that uses ephemeral wetlands and the upland habitat (scrub, mesic flatwoods, and sandhills) that surrounds those wetlands. -
The Quarterly Journal of the Florida Native Plant Society
Volume 28: Number 1 > Winter/Spring 2011 PalmettoThe Quarterly Journal of the Florida Native Plant Society Protecting Endangered Plants in Panhandle Parks ● Native or Not? Carica papaya ● Water Science & Plants Protecting Endangered Plant Species Sweetwater slope: Bill and Pam Anderson To date, a total of 117 listed taxa have been recorded in 26 panhandle parks, making these parks a key resource for the protection of endangered plant species. 4 ● The Palmetto Volume 28:1 ● Winter/Spring 2011 in Panhandle State Parks by Gil Nelson and Tova Spector The Florida Panhandle is well known for its natural endowments, chief among which are its botanical and ecological diversity. Approximately 242 sensitive plant taxa occur in the 21 counties west of the Suwannee River. These include 15 taxa listed as endangered or threatened by the U. S. Fish and Wildlife Service (USFWS), 212 listed as endangered or threatened by the State of Florida, 191 tracked by the Florida Natural Areas Inventory, 52 candidates for federal listing, and 7 categorized by the state as commercially exploited. Since the conservation of threatened and endangered plant species depends largely on effective management of protected populations, the occurrence of such plants on publicly or privately owned conservation lands, coupled with institutional knowledge of their location and extent is essential. District 1 of the Florida Sarracenia rosea (purple pitcherplant) at Ponce de Leon Springs State Park: Park Service manages 33 state parks encompassing approximately Tova Spector, Florida Department of Environmental Protection 53,877 acres in the 18 counties from Jefferson County and the southwestern portion of Taylor County westward. -
Torreya Taxifolia
photograph © Abraham Rammeloo Torreya taxifolia produces seeds in 40 Kalmthout Arboretum ABRAHAM RAMMELOO, Curator of the Kalmthout Arboretum, writes about this rare conifer that recently produced seed for the first time. Torreya is a genus of conifers that comprises four to six species that are native to North America and Asia. It is closely related to Taxus and Cephalotaxus and is easily confused with the latter. However, it is relatively easy to distinguish them apart by their leaves. Torreya has needles with, on the underside, two small edges with stomas giving it a green appearance; Cephalotaxus has different rows of stomas, and for this reason the underside is more of a white colour. It is very rare to find Torreya taxifolia in the wild; it is native to a small area in Florida and Georgia. It grows in steep limestone cliffs along the Apalachicola River. These trees come from a warm and humid climate where the temperature in winter occasionally falls below freezing. They grow mainly on north-facing slopes between Fagus grandifolia, Liriodendron tulipifera, Acer barbatum, Liquidambar styraciflua and Quercus alba. They can grow up to 15 to 20 m high. The needles are sharp and pointed and grow in a whorled pattern along the branches. They are 25 to 35 mm long and stay on the tree for three to four years. If you crush them, they give off a strong, sharp odour. The health and reproduction of the adult population of this species suffered INTERNATIONAL DENDROLOGY SOCIETY TREES Opposite Torreya taxifolia ‘Argentea’ growing at Kalmthout Arboretum in Belgium. -
PHYLOGENETIC RELATIONSHIPS of TORREYA (TAXACEAE) INFERRED from SEQUENCES of NUCLEAR RIBOSOMAL DNA ITS REGION Author(S): Jianhua Li, Charles C
PHYLOGENETIC RELATIONSHIPS OF TORREYA (TAXACEAE) INFERRED FROM SEQUENCES OF NUCLEAR RIBOSOMAL DNA ITS REGION Author(s): Jianhua Li, Charles C. Davis, Michael J. Donoghue, Susan Kelley and Peter Del Tredici Source: Harvard Papers in Botany, Vol. 6, No. 1 (July 2001), pp. 275-281 Published by: Harvard University Herbaria Stable URL: http://www.jstor.org/stable/41761652 Accessed: 14-06-2016 15:35 UTC REFERENCES Linked references are available on JSTOR for this article: http://www.jstor.org/stable/41761652?seq=1&cid=pdf-reference#references_tab_contents You may need to log in to JSTOR to access the linked references. Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at http://about.jstor.org/terms JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. Harvard University Herbaria is collaborating with JSTOR to digitize, preserve and extend access to Harvard Papers in Botany This content downloaded from 128.103.224.4 on Tue, 14 Jun 2016 15:35:14 UTC All use subject to http://about.jstor.org/terms PHYLOGENETIC RELATIONSHIPS OF TORREYA (TAXACEAE) INFERRED FROM SEQUENCES OF NUCLEAR RIBOSOMAL DNA ITS REGION Jianhua Li,1 Charles C. Davis,2 Michael J. Donoghue,3 Susan Kelley,1 And Peter Del Tredici1 Abstract. Torreya, composed of five to seven species, is distributed disjunctly in eastern Asia and the eastern and western United States. -
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S. Fish and Wildlife Service Region 4—An Update April 2013 Prepared by: Pam L. Fuller, Amy J. Benson, and Matthew J. Cannister U.S. Geological Survey Southeast Ecological Science Center Gainesville, Florida Prepared for: U.S. Fish and Wildlife Service Southeast Region Atlanta, Georgia Cover Photos: Silver Carp, Hypophthalmichthys molitrix – Auburn University Giant Applesnail, Pomacea maculata – David Knott Straightedge Crayfish, Procambarus hayi – U.S. Forest Service i Table of Contents Table of Contents ...................................................................................................................................... ii List of Figures ............................................................................................................................................ v List of Tables ............................................................................................................................................ vi INTRODUCTION ............................................................................................................................................. 1 Overview of Region 4 Introductions Since 2000 ....................................................................................... 1 Format of Species Accounts ...................................................................................................................... 2 Explanation of Maps ................................................................................................................................ -
Prioritizing Regions for the Conservation of Amphibians With
PRIORITIZING REGIONS FOR THE CONSERVATION OF AMPHIBIANS WITH SPECIAL EMPHASIS ON THE RED HILLS SALAMANDER (PHAEOGNATHUS HUBRICHTI) by JOSEPH J. APODACA A DISSERTATION Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Biological Sciences in the Graduate School of The University of Alabama TUSCALOOSA, ALABAMA 2010 Copyright Joseph J. Apodaca 2010 ALL RIGHTS RESERVED ABSTRACT Amphibians are the most threatened vertebrate group in the world, and are experiencing rapid species declines and numerous extinctions. The most effective way to stem these losses is through the establishment of protected areas. The limited amount of funding available to such efforts requires that conservation agencies and biologists must find a way to properly focus their efforts and resources. Yet, there is no clear-cut method to prioritize areas for biological reserves. In fact, the identification of biologically important regions is one of the most debated topics in the field of conservation biology. As this debate wages on and as species continue to decline at an unprecedented rate, conservation biologists have come to rely on increasingly sophisticated methods for the identification of these areas. In this dissertation I focus on recently developed techniques for prioritizing reserve selection from macro to micro-scales for amphibians in the southeastern United States. For chapters one and two I focus on broad scale issues for wide taxonomic groups. Chapter one focuses on testing whether using environmental niche models rather than extent of occurrence maps to create richness patterns is a valid approach. I found that environmental niche models could be useful for generating richness patterns for understudied regions or taxa if proper precautions are taken. -
Variations in Tetrodotoxin Levels in Populations of Taricha Granulosa
www.nature.com/scientificreports OPEN Variations in tetrodotoxin levels in populations of Taricha granulosa are expressed in the morphology of their cutaneous glands Pedro Luiz Mailho-Fontana1*, Carlos Jared1, Marta Maria Antoniazzi1, Juliana Mozer Sciani 2, Daniel Carvalho Pimenta 1, Amber N. Stokes3, Taran Grant4, Edmund D. Brodie III5 & Edmund D. Brodie Jr.6 Tetrodotoxin (TTX), one of the most toxic substances in nature, is present in bacteria, invertebrates, fshes, and amphibians. Marine organisms seem to bioaccumulate TTX from their food or acquire it from symbiotic bacteria, but its origin in amphibians is unclear. Taricha granulosa can exhibit high TTX levels, presumably concentrated in skin poison glands, acting as an agent of selection upon predatory garter snakes (Thamnophis). This co-evolutionary arms race induces variation in T. granulosa TTX levels, from very high to undetectable. Using morphology and biochemistry, we investigated diferences in toxin localization and quality between two populations at the extremes of toxicity. TTX concentration within poison glands is related to the volume of a single cell type in which TTX occurs exclusively in distinctive secretory granules, suggesting a relationship between granule structure and chemical composition. TTX was detected in mucous glands in both populations, contradicting the general understanding that these glands do not secrete defensive chemicals and expanding currently held interpretations of amphibian skin gland functionality. Skin secretions of the two populations difered in low-mass molecules and proteins. Our results demonstrate that interpopulation variation in TTX levels is related to poison gland morphology. Tetrodotoxin (TTX) is one of the most toxic and well-studied but still mysterious natural products. -
Fusarium Torreyae (Sp
HOST RANGE AND BIOLOGY OF FUSARIUM TORREYAE (SP. NOV), CAUSAL AGENT OF CANKER DISEASE OF FLORIDA TORREYA (TORREYA TAXIFOLIA ARN.) By AARON J. TRULOCK A THESIS PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE UNIVERSITY OF FLORIDA 2012 1 © 2012 Aaron J. Trulock 2 To my wife, for her support, patience, and dedication 3 ACKNOWLEDGMENTS I would like to thank my chair, Jason Smith, and committee members, Jenny Cruse-Sanders and Patrick Minogue, for their guidance, encouragement, and boundless knowledge, which has helped me succeed in my graduate career. I would also like to thank the Forest Pathology lab for aiding and encouraging me in both my studies and research. Research is not an individual effort; it’s a team sport. Without wonderful teammates it would never happen. Finally, I would like to that the U.S. Forest Service for their financial backing, as well as, UF/IFAS College of Agriculture and Life Science for their matching funds. 4 TABLE OF CONTENTS page ACKNOWLEDGMENTS .................................................................................................. 4 LIST OF TABLES ............................................................................................................ 6 LIST OF FIGURES .......................................................................................................... 7 ABSTRACT ..................................................................................................................... 8 -
AMPHIBIANS of OHIO F I E L D G U I D E DIVISION of WILDLIFE INTRODUCTION
AMPHIBIANS OF OHIO f i e l d g u i d e DIVISION OF WILDLIFE INTRODUCTION Amphibians are typically shy, secre- Unlike reptiles, their skin is not scaly. Amphibian eggs must remain moist if tive animals. While a few amphibians Nor do they have claws on their toes. they are to hatch. The eggs do not have are relatively large, most are small, deli- Most amphibians prefer to come out at shells but rather are covered with a jelly- cately attractive, and brightly colored. night. like substance. Amphibians lay eggs sin- That some of these more vulnerable spe- gly, in masses, or in strings in the water The young undergo what is known cies survive at all is cause for wonder. or in some other moist place. as metamorphosis. They pass through Nearly 200 million years ago, amphib- a larval, usually aquatic, stage before As with all Ohio wildlife, the only ians were the first creatures to emerge drastically changing form and becoming real threat to their continued existence from the seas to begin life on land. The adults. is habitat degradation and destruction. term amphibian comes from the Greek Only by conserving suitable habitat to- Ohio is fortunate in having many spe- amphi, which means dual, and bios, day will we enable future generations to cies of amphibians. Although generally meaning life. While it is true that many study and enjoy Ohio’s amphibians. inconspicuous most of the year, during amphibians live a double life — spend- the breeding season, especially follow- ing part of their lives in water and the ing a warm, early spring rain, amphib- rest on land — some never go into the ians appear in great numbers seemingly water and others never leave it. -
Abundance, Distribution, Population Structure, and Substrate Use of Ambystoma Altamirani Along the Arroyo Los Axolotes, State of Mexico, Mexico
Herpetological Conservation and Biology 15(1):188–197. Submitted: 16 August 2019; Accepted: 23 February 2020; Published: 30 April 2020. ABUNDANCE, DISTRIBUTION, POPULATION STRUCTURE, AND SUBSTRATE USE OF AMBYSTOMA ALTAMIRANI ALONG THE ARROYO LOS AXOLOTES, STATE OF MEXICO, MEXICO VIRIDIANA VILLARREAL HERNÁNDEZ1, GEOFFREY R. SMITH2, RAYMUNDO MONTOYA AYALA3, AND JULIO A. LEMOS-ESPINAL1,4 1Laboratorio de Ecología - Unidad de Biotecnología y Prototipos, Facultad de Estudios Superiores Iztacala, Avendina Los Barrios 1, Los Reyes Iztacala, Tlalnepantla, Estado de México, 54090, México 2Department of Biology, Denison University, Granville, Ohio 43023, USA 3Laboratorio de Cómputo - Unidad de Biotecnología y Prototipos, Facultad de Estudios Superiores Iztacala, Avenida Los Barrios 1, Los Reyes Iztacala, Tlalnepantla, Estado de México, 54090, México 4Corresponding author: e-mail: [email protected] Abstract.—Ambystomatid salamanders in central Mexico are confronted by anthropogenic threats that can limit their distribution and abundance. Ambystoma altamirani (Mountain Stream Siredon) is listed as Endangered by the International Union for Conservation of Nature (IUCN) Red List and as Threatened by the Mexican government. We report on the distribution, abundance, occupancy, population structure, and substrate use of A. altamirani, a stream dwelling salamander, along the Arroyo los Axolotes, Sierra de las Cruces, Mexico. We observed A. altamirani at least once during repeated surveys between February 2018 to December 2018 in 24 of 25 permanent 5-m long reaches separated by 40 m. The best model for occupancy had constant occupancy, detection, extinction, and colonization probabilities. Sites that dried at some time during the study had fewer observed individuals than those that did not dry. Size structure was relatively constant throughout the year, except for the appearance of small larvae in May, June, and July. -
The Salamanders of Tennessee
Salamanders of Tennessee: modified from Lisa Powers tnwildlife.org Follow links to Nongame The Salamanders of Tennessee Photo by John White Salamanders are the group of tailed, vertebrate animals that along with frogs and caecilians make up the class Amphibia. Salamanders are ectothermic (cold-blooded), have smooth glandular skin, lack claws and must have a moist environment in which to live. 1 Amphibian Declines Worldwide, over 200 amphibian species have experienced recent population declines. Scientists have reports of 32 species First discovered in 1967, the golden extinctions, toad, Bufo periglenes, was last seen mainly species of in 1987. frogs. Much attention has been given to the Anurans (frogs) in recent years, however salamander populations have been poorly monitored. Photo by Henk Wallays Fire Salamander - Salamandra salamandra terrestris 2 Why The Concern For Salamanders in Tennessee? Their key role and high densities in many forests The stability in their counts and populations Their vulnerability to air and water pollution Their sensitivity as a measure of change The threatened and endangered status of several species Their inherent beauty and appeal as a creature to study and conserve. *Possible Factors Influencing Declines Around the World Climate Change Habitat Modification Habitat Fragmentation Introduced Species UV-B Radiation Chemical Contaminants Disease Trade in Amphibians as Pets *Often declines are caused by a combination of factors and do not have a single cause. Major Causes for Declines in Tennessee Habitat Modification -The destruction of natural habitats is undoubtedly the biggest threat facing amphibians in Tennessee. Housing, shopping center, industrial and highway construction are all increasing throughout the state and consequently decreasing the amount of available habitat for amphibians.