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SDG Indicator Metadata (Harmonized Metadata Template - Format Version 1.0)
Last updated: 4 January 2021 SDG indicator metadata (Harmonized metadata template - format version 1.0) 0. Indicator information 0.a. Goal Goal 15: Protect, restore and promote sustainable use of terrestrial ecosystems, sustainably manage forests, combat desertification, and halt and reverse land degradation and halt biodiversity loss 0.b. Target Target 15.5: Take urgent and significant action to reduce the degradation of natural habitats, halt the loss of biodiversity and, by 2020, protect and prevent the extinction of threatened species 0.c. Indicator Indicator 15.5.1: Red List Index 0.d. Series 0.e. Metadata update 4 January 2021 0.f. Related indicators Disaggregations of the Red List Index are also of particular relevance as indicators towards the following SDG targets (Brooks et al. 2015): SDG 2.4 Red List Index (species used for food and medicine); SDG 2.5 Red List Index (wild relatives and local breeds); SDG 12.2 Red List Index (impacts of utilisation) (Butchart 2008); SDG 12.4 Red List Index (impacts of pollution); SDG 13.1 Red List Index (impacts of climate change); SDG 14.1 Red List Index (impacts of pollution on marine species); SDG 14.2 Red List Index (marine species); SDG 14.3 Red List Index (reef-building coral species) (Carpenter et al. 2008); SDG 14.4 Red List Index (impacts of utilisation on marine species); SDG 15.1 Red List Index (terrestrial & freshwater species); SDG 15.2 Red List Index (forest-specialist species); SDG 15.4 Red List Index (mountain species); SDG 15.7 Red List Index (impacts of utilisation) (Butchart 2008); and SDG 15.8 Red List Index (impacts of invasive alien species) (Butchart 2008, McGeoch et al. -
Critically Endangered - Wikipedia
Critically endangered - Wikipedia Not logged in Talk Contributions Create account Log in Article Talk Read Edit View history Critically endangered From Wikipedia, the free encyclopedia Main page Contents This article is about the conservation designation itself. For lists of critically endangered species, see Lists of IUCN Red List Critically Endangered Featured content species. Current events A critically endangered (CR) species is one which has been categorized by the International Union for Random article Conservation status Conservation of Nature (IUCN) as facing an extremely high risk of extinction in the wild.[1] Donate to Wikipedia by IUCN Red List category Wikipedia store As of 2014, there are 2464 animal and 2104 plant species with this assessment, compared with 1998 levels of 854 and 909, respectively.[2] Interaction Help As the IUCN Red List does not consider a species extinct until extensive, targeted surveys have been About Wikipedia conducted, species which are possibly extinct are still listed as critically endangered. IUCN maintains a list[3] Community portal of "possibly extinct" CR(PE) and "possibly extinct in the wild" CR(PEW) species, modelled on categories used Recent changes by BirdLife International to categorize these taxa. Contact page Contents Tools Extinct 1 International Union for Conservation of Nature definition What links here Extinct (EX) (list) 2 See also Related changes Extinct in the Wild (EW) (list) 3 Notes Upload file Threatened Special pages 4 References Critically Endangered (CR) (list) Permanent -
A Summary of Vulnerability of Habitats and Priority Species
Climate Change and Biodiversity in Maine: A Summary of Vulnerability of Habitats and Priority Species Andrew Whitman Phillip deMaynadier Barbara Vickery Manomet Center for Conservation Sciences ME Department of Inland Fisheries and The Nature Conservancy Andrew Cutko Wildlife Sally Stockwell ME Department of Agriculture, Conservation, Steve Walker Maine Audubon and Forestry Maine Coast Heritage Trust Robert Houston U.S. Fish and Wildlife Service Introduction As we watch temperatures climb and experience extremes in weather, it is clear that climate change has become a tangible threat to Maine’s ecosystems. Long-term research has shown that Maine’s wildlife are already responding to climate change.1 We will likely lose some of Maine’s native wildlife and observe permanent changes to their habitats in the coming decades. By 2100, average temperatures may increase 3° to 13°F. In response, the predicted northward shift of species ranges has begun. Rising temperatures will allow pests such as Winter Moose Tick (Dermacentor albipictus) and Hemlock Wooly Adelgid (Adelges tsugae) to become more common, potentially harming native wildlife and their habitats. Drought may occur more frequently and impact all habitats, especially wetlands. Sea level will likely rise three to six feet and will flood coastal marshes and beaches. Recognizing these challenges, a team of Maine scientists assessed the vulnerability of wildlife and habitats to a changing climate and then identified general strategies to reduce their vulnerability.2 Other states have taken this first step as they aim to update their state wildlife action plans (SWAPs) by 2015. States originally created SWAPs to set conservation priorities and obtain additional federal funding for wildlife. -
The Economics of Threatened Species Conservation: a Review and Analysis
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 2009 The Economics of Threatened Species Conservation: A Review and Analysis Ray T. Sterner U.S. Department of Agriculture, Animal and Plant Health Inspection Service, National Wildlife Research Center, Fort Collins, Colorado Follow this and additional works at: https://digitalcommons.unl.edu/icwdm_usdanwrc Part of the Environmental Sciences Commons Sterner, Ray T., "The Economics of Threatened Species Conservation: A Review and Analysis" (2009). USDA National Wildlife Research Center - Staff Publications. 978. https://digitalcommons.unl.edu/icwdm_usdanwrc/978 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. In: ÿ and book of Nature Conservation ISBN 978-1 -60692-993-3 Editor: Jason B. Aronoff O 2009 Nova Science Publishers, Inc. Chapter 8 Ray T. Sterner1 U.S. Department of Agriculture, Animal and Plant Health Inspection Service, National Wildlife Research Center, Fort Collins, Colorado 80521-2154, USA Stabilizing human population size and reducing human-caused impacts on the environment are lceys to conserving threatened species (TS). Earth's human population is =: 7 billion and increasing by =: 76 million per year. This equates to a human birth-death ratio of 2.35 annually. The 2007 Red List prepared by the International Union for Conservation of Nature and Natural Resources (IUCN) categorized 16,306 species of vertebrates, invertebrates, plants, and other organisms (e.g., lichens, algae) as TS. -
Status and Protection of Globally Threatened Species in the Caucasus
STATUS AND PROTECTION OF GLOBALLY THREATENED SPECIES IN THE CAUCASUS CEPF Biodiversity Investments in the Caucasus Hotspot 2004-2009 Edited by Nugzar Zazanashvili and David Mallon Tbilisi 2009 The contents of this book do not necessarily reflect the views or policies of CEPF, WWF, or their sponsoring organizations. Neither the CEPF, WWF nor any other entities thereof, assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, product or process disclosed in this book. Citation: Zazanashvili, N. and Mallon, D. (Editors) 2009. Status and Protection of Globally Threatened Species in the Caucasus. Tbilisi: CEPF, WWF. Contour Ltd., 232 pp. ISBN 978-9941-0-2203-6 Design and printing Contour Ltd. 8, Kargareteli st., 0164 Tbilisi, Georgia December 2009 The Critical Ecosystem Partnership Fund (CEPF) is a joint initiative of l’Agence Française de Développement, Conservation International, the Global Environment Facility, the Government of Japan, the MacArthur Foundation and the World Bank. This book shows the effort of the Caucasus NGOs, experts, scientific institutions and governmental agencies for conserving globally threatened species in the Caucasus: CEPF investments in the region made it possible for the first time to carry out simultaneous assessments of species’ populations at national and regional scales, setting up strategies and developing action plans for their survival, as well as implementation of some urgent conservation measures. Contents Foreword 7 Acknowledgments 8 Introduction CEPF Investment in the Caucasus Hotspot A. W. Tordoff, N. Zazanashvili, M. Bitsadze, K. Manvelyan, E. Askerov, V. Krever, S. Kalem, B. Avcioglu, S. Galstyan and R. Mnatsekanov 9 The Caucasus Hotspot N. -
(GISD) 2021. Species Profile Rattus Rattus. Available From
FULL ACCOUNT FOR: Rattus rattus Rattus rattus System: Terrestrial Kingdom Phylum Class Order Family Animalia Chordata Mammalia Rodentia Muridae Common name Hausratte (German), European house rat (English), bush rat (English), blue rat (English), ship rat (English), roof rat (English), black rat (English) Synonym Mus rattus , Linnaeus, 1758 Mus alexandrinus , Geoffroy, 1803 Musculus frugivorus , Rafinesque, 1814 Mus novaezelandiae , Buller, 1870 Similar species Rattus norvegicus Summary A native of the Indian sub-continent, the ship rat (Rattus rattus) has now spread throughout the world. It is widespread in forest and woodlands as well as being able to live in and around buildings. It will feed on and damage almost any edible thing. The ship rat is most frequently identified with catastrophic declines of birds on islands. It is very agile and often frequents tree tops searching for food and nesting there in bunches of leaves and twigs. view this species on IUCN Red List Species Description A slender rat with large hairless ears, the ship rat (Rattus rattus) may be grey-brown on the back with either a similarly coloured or creamish-white belly, or it may be black all over. The uniformly- coloured tail is always longer than the head and body length combined. Its body weight is usually between 120 and 160 g but it can exceed 200 g. The work of Yosida (1980) and his co-workers has shown that there are two forms of R. rattus that differ in chromosome number. The more widespread Oceanic form has 38 chromosomes and is the ship rat of Europe, the Mediterranean region, America, Australia and New Zealand. -
Listing a Species As a Threatened Or Endangered Species Section 4 of the Endangered Species Act
U.S. Fish & Wildlife Service Listing a Species as a Threatened or Endangered Species Section 4 of the Endangered Species Act The Endangered Species Act of 1973, as amended, is one of the most far- reaching wildlife conservation laws ever enacted by any nation. Congress, on behalf of the American people, passed the ESA to prevent extinctions facing many species of fish, wildlife and plants. The purpose of the ESA is to conserve endangered and threatened species and the ecosystems on which they depend as key components of America’s heritage. To implement the ESA, the U.S. Fish and Wildlife Service works in cooperation with the National Marine Fisheries Service (NMFS), other Federal, State, and local USFWS Susanne Miller, agencies, Tribes, non-governmental Listed in 2008 as threatened because of the decline in sea ice habitat, the polar bear may organizations, and private citizens. spend time on land during fall months, waiting for ice to return. Before a plant or animal species can receive the protection provided by What are the criteria for deciding whether refer to these species as “candidates” the ESA, it must first be added to to add a species to the list? for listing. Through notices of review, the Federal lists of threatened and A species is added to the list when it we seek biological information that will endangered wildlife and plants. The is determined to be an endangered or help us to complete the status reviews List of Endangered and Threatened threatened species because of any of for these candidate species. We publish Wildlife (50 CFR 17.11) and the List the following factors: notices in the Federal Register, a daily of Endangered and Threatened Plants n the present or threatened Federal Government publication. -
Chapter XXV —Class Oligochaeta
Chapter XXV —Class Oligochaeta (Aquatic Worms)- Phylum Annelida Oligochaetes are common in most freshwater habitats, but they are often ignored by freshwater biologists because they are thought to be extraordinarily difficult to identify. The extensive taxo- nomic work done since 1960 by Brinkhurst and others, however, has enabled routine identifica- tion of most of our freshwater oligochaetes from simple whole mounts. Some aquatic worms closely resemble terrestrial earthworms while others can be much narrower or thread-like. Many aquatic worms can tolerate low dissolved oxygen and may be found in large numbers in organi- cally polluted habitats. Aquatic worms can be distinguished by: (Peckarsky et al., 1990) • Body colour may be red, tan, brown or black. • Cylindrical, thin (some are very thin), segmented body may be upto 5 inches. • May have short bristles or hairs (setae) that help with movement (usually not visible). • Moves by stretching and pulling its body along in a worm-like fashion. Four families in the orders Tubificida and Lumbriculida are common in freshwater in northeastern North America: the Tubificidae, Naididae, Lumbriculidae, and Enchytraeidae. In addition, fresh- water biologists sometimes encounter lumbricine oligochaetes (order Lumbricina; the familiar earthworms), haplotaxid oligochaetes (order Haplotaxida; rare inhabitants of groundwater), Aeolosoma (class Aphanoneura; small worms once classified with the oligochaetes), and Manayunkia speciosa (class Polychaeta) in waters of northeastern North America. (Peckarsky et al., 1990). The two families, Naididae and Tubificidae form 80 to 100% of the annelid communi- ties in the benthos of most streams and lakes at all trophic levels. They range in size from 0.1 cm in Naididae to 3 or 4 cm in relaxed length in Lumbricidae, the family that contains the earth- worms. -
Reforestation with Native Species in the Dry Lands of Panama
Reforestation with Native Species in the Dry Lands of Panama Raíces Nativas Carla Chízmar, José De Gracia & Mauricio Hoyos Conservation Leadership Programme: Final Report ID: 02141513 Project name: Reforestation with Native Species in the Dry Lands of Panama Host country/site location: Republic of Panama/La Toza, Nata, Cocle Authors: Carla Chízmar, Mauricio Hoyos and José De Gracia Contact address: Bella Vista, #37, 2A, Panama, Republic of Panama. E-mail [email protected] [email protected] Website: https://www.facebook.com/reforestaciontoza Date completed: September 24th, 2015 2 Conservation Leadership Programme: Final Report Table of Contents Project Partners & Collaborators Page 4 Section 1 Summary Page 4 Introduction Page 5 Project members Page 5 Section 2 Aim and objectives Page 6 Changes to original project plan Page 6 Methodology Page 7 Outputs and Results Page 7 Communication & Application of results Page 15 Monitoring and Evaluation Page 15 Achievements and Impacts Page 16 Capacity Development and Leadership capabilities Page 17 Section 3 Conclusion Page 17 Problems encountered and lessons learnt Page 17 In the future Page 18 Financial Report Page 19 Section 4 Appendices Page 19 3 Conservation Leadership Programme: Final Report Project Partners & Collaborators Miambiente - Panama's environmental ministry regulates all activities affecting the protection, conservation, improvement and restoration of the country's environment. Formerly known as environment authority ANAM. They helped us with trainers and seeds to start the nursery facilities. Ministry of Education of Panama - They supported us with the space for nursery facilities and permitted us to develop all the training activities in the local school grounds. -
Population Genetics of the Native Rodents of the Galápagos Islands, Ecuador
Population Genetics of the Native Rodents of the Galápagos Islands, Ecuador A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy at George Mason University By Sarah Johnson Master of Science Stephen F. Austin State University, 2005 Bachelor of Science Texas A&M University, 2003 Director: Dr. Cody W. Edwards, Assistant Professor Department of Environmental Science and Public Policy Summer Semester 2009 George Mason University Fairfax, VA Copyright 2009 Sarah Johnson All Rights Reserved ii ACKNOWLEDGMENTS I would like to thank my parents (Michael and Kay Johnson) and my sisters (Kris and Faith) for their unwavering support throughout my academic career. This dissertation is lovingly dedicated to my parents. I would like to thank my Aggie Family (Brad and Kristin Atchison, Reece and Erin Flood, Samir Moussa, Doug Fuentes, and the rest of the IV Horsemen). They have always lovingly provided a shoulder to lean on and kind ear willing to listen. I would like to thank my fellow graduate students at GMU (Jeff Streicher, Mike Jarcho, Kat Bryant, Tammy Henry, Geoff Cook, Ryan Peters, Kristin Wolf, Trishna Dutta, Sandeep Sharma, and Jolanda Luksenburg) for their help in the field, lab, classroom, and all aspects of student life. I am eternally indebted to Dr. Pat Gillevet and Masi Sikaroodi for their invaluable assistance in the lab, and to Dr. Jesús Maldonado for his assistance in writing the dissertation. They are infinite sources of help and support for which I am forever grateful. The project would not have been possible without Dr. Cody W. Edwards and Dr. -
The Neotropical Region Sensu the Areas of Endemism of Terrestrial Mammals
Australian Systematic Botany, 2017, 30, 470–484 ©CSIRO 2017 doi:10.1071/SB16053_AC Supplementary material The Neotropical region sensu the areas of endemism of terrestrial mammals Elkin Alexi Noguera-UrbanoA,B,C,D and Tania EscalanteB APosgrado en Ciencias Biológicas, Unidad de Posgrado, Edificio A primer piso, Circuito de Posgrados, Ciudad Universitaria, Universidad Nacional Autónoma de México (UNAM), 04510 Mexico City, Mexico. BGrupo de Investigación en Biogeografía de la Conservación, Departamento de Biología Evolutiva, Facultad de Ciencias, Universidad Nacional Autónoma de México (UNAM), 04510 Mexico City, Mexico. CGrupo de Investigación de Ecología Evolutiva, Departamento de Biología, Universidad de Nariño, Ciudadela Universitaria Torobajo, 1175-1176 Nariño, Colombia. DCorresponding author. Email: [email protected] Page 1 of 18 Australian Systematic Botany, 2017, 30, 470–484 ©CSIRO 2017 doi:10.1071/SB16053_AC Table S1. List of taxa processed Number Taxon Number Taxon 1 Abrawayaomys ruschii 55 Akodon montensis 2 Abrocoma 56 Akodon mystax 3 Abrocoma bennettii 57 Akodon neocenus 4 Abrocoma boliviensis 58 Akodon oenos 5 Abrocoma budini 59 Akodon orophilus 6 Abrocoma cinerea 60 Akodon paranaensis 7 Abrocoma famatina 61 Akodon pervalens 8 Abrocoma shistacea 62 Akodon philipmyersi 9 Abrocoma uspallata 63 Akodon reigi 10 Abrocoma vaccarum 64 Akodon sanctipaulensis 11 Abrocomidae 65 Akodon serrensis 12 Abrothrix 66 Akodon siberiae 13 Abrothrix andinus 67 Akodon simulator 14 Abrothrix hershkovitzi 68 Akodon spegazzinii 15 Abrothrix illuteus -
Chromosomal Relationships Among the Native Rodents (Cricetidae: Oryzomyini) of the Galápagos Islands, Ecuador
THERYA, 2021, Vol. 12(2):317-329 DOI:10.12933/therya-21-1126 ISSN 2007-3364 Chromosomal relationships among the native rodents (Cricetidae: Oryzomyini) of the Galápagos Islands, Ecuador ROBERT C. DOWLER1* AND MArcIA A. REVELEZ2 1 Department of Biology, Angelo State University, San Angelo 76909. Texas, USA. E-mail: [email protected]. 2 Museum of Texas Tech University, Lubbock 76409-3191. Texas, USA, E-mail: [email protected]. *Corresponding author Although the Galápagos Islands are recognized for their contribution to our understanding of evolutionary theory and have received the attention of scientists for over 185 years, our understanding of the native rodents there has been minimal relative to many other groups of organisms. Much of what we knew through most of the 20th century was based solely on species descriptions. Chromosome data has been limited to only Nesoryzomys narboroughi (2n = 32, FN (number of autosomal arms) = 50) and Aegialomys galapagoensis (2n = 56; FN = 58). We present the karyotypes of the only remaining extant species in the genus, N. swarthi (2n = 56; FN = 54) and N. fernandinae (2n = 44; FN = 54). Chromosomal banding reveals that extensive rearrangement has occurred within Nesoryzomys, including Robertsonian fusion and tandem fusion events but these alone cannot account for the diverse diploid numbers found within the genus. We propose that 1) N. swarthi repre- sents the ancestral karyotype for the genus, similar to A. galapagoensis, 2) N. swarthi and N. fernandinae share the same fundamental number, suggesting divergence by Robertsonian fusions, and 3) N. narboroughi has the most derived karyotype, based on banding morphology and low diploid number.