Status and Conservation of Shearwaters of the North Pacific
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Table 7: Species Changing IUCN Red List Status (2014-2015)
IUCN Red List version 2015.4: Table 7 Last Updated: 19 November 2015 Table 7: Species changing IUCN Red List Status (2014-2015) Published listings of a species' status may change for a variety of reasons (genuine improvement or deterioration in status; new information being available that was not known at the time of the previous assessment; taxonomic changes; corrections to mistakes made in previous assessments, etc. To help Red List users interpret the changes between the Red List updates, a summary of species that have changed category between 2014 (IUCN Red List version 2014.3) and 2015 (IUCN Red List version 2015-4) and the reasons for these changes is provided in the table below. IUCN Red List Categories: EX - Extinct, EW - Extinct in the Wild, CR - Critically Endangered, EN - Endangered, VU - Vulnerable, LR/cd - Lower Risk/conservation dependent, NT - Near Threatened (includes LR/nt - Lower Risk/near threatened), DD - Data Deficient, LC - Least Concern (includes LR/lc - Lower Risk, least concern). Reasons for change: G - Genuine status change (genuine improvement or deterioration in the species' status); N - Non-genuine status change (i.e., status changes due to new information, improved knowledge of the criteria, incorrect data used previously, taxonomic revision, etc.); E - Previous listing was an Error. IUCN Red List IUCN Red Reason for Red List Scientific name Common name (2014) List (2015) change version Category Category MAMMALS Aonyx capensis African Clawless Otter LC NT N 2015-2 Ailurus fulgens Red Panda VU EN N 2015-4 -
The Short-Tailed Shearwater: a Review of Its Biology
Corella, 1991 , 15(2): 45-52 A11srralasia11 Hird l?<'l'iews - N11111ber 3 THE SHORT-TAILED SHEARWATER: A REVIEW OF ITS BIOLOGY IRYNEJ SKIRA Department of Parks. Wiltllifc and Heritage, 134 Macquarie St.. Hobart. Tas 7000 {<eceived I May /990 The life history of the Short-tailed Shearwater Puffinus tenuirostris has been well documented since it first came to the attention of naturalists. Approximately 23 million birds breed in about 250 colonies in southeastern Australia from September to April. The Short-tailed Shearwater commences to breed when 4 to 15 years. During their completed lifetimes 27 per cent of all individuals produce no young and 19 per cent only one chick. Mortality is age-related with the median survival time for breeding being 9.3 years after first breeding. Many areas remain open for study, with a particular need for interdisciplinary research that includes oceanography. INTRODUCTION The Short-tailed Shearwater was one of the first Australian birds to be banded in large numbers The Short-tailed Shearwater Puffinustenuirostris, (Serventy 1957, 1961) and to be subjected to a commonly known as the Tasmanian muttonbird, long-term scientific study (Guiler et al. 1958). This is one of about I 00 species in the Procellarii study was commenced on Fisher Island in the formes. The diagno�tic feature of the order is the Furneaux Group of Tasmania in March 1947 by external nostrils produced into tubes extending Dominic Serventy formerly of the CSIRO onto the bill. Other distinctive features are the (Scrventy 1977) and continues to the present. 42 hooked and plated bill. -
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Vol. 651: 163–181, 2020 MARINE ECOLOGY PROGRESS SERIES Published October 1 https://doi.org/10.3354/meps13439 Mar Ecol Prog Ser OPEN ACCESS Habitat preferences, foraging behaviour and bycatch risk among breeding sooty shearwaters Ardenna grisea in the Southwest Atlantic Anne-Sophie Bonnet-Lebrun1,2,3,8,*, Paulo Catry1, Tyler J. Clark4,9, Letizia Campioni1, Amanda Kuepfer5,6,7, Megan Tierny6, Elizabeth Kilbride4, Ewan D. Wakefield4 1MARE − Marine and Environmental Sciences Centre, ISPA - Instituto Universitário, Rua Jardim do Tabaco 34, 1149-041 Lisboa, Portugal 2Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK 3Centre d’Ecologie Fonctionnelle et Evolutive CEFE UMR 5175, CNRS — Université de Montpellier - Université Paul-Valéry Montpellier — EPHE, 34293 Montpellier cedex 5, France 4Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow G12 8QQ, UK 5FIFD — Falkland Islands Fisheries Department, Falkland Islands Government, PO Box 598, Stanley, Falkland Islands, FIQQ 1ZZ, UK 6SAERI — South Atlantic Environmental Research Institute, Stanley, Falkland Islands, FIQQ 1ZZ, UK 7Environment and Sustainability Institute, University of Exeter, Penryn Campus, Penryn TR10 9FE, UK 8Present address: British Antarctic Survey, High Cross, Madingley Road, Cambridge CB4 0ET, UK 9Present address: Wildlife Biology Program, Department of Ecosystem and Conservation Sciences, W.A. Franke College of Forestry and Conservation, University of Montana, 32 Campus Drive, Missoula, Montana 59812, USA ABSTRACT: Pelagic seabirds are important components of many marine ecosystems. The most abundant species are medium/small sized petrels (<1100 g), yet the sub-mesoscale (<10 km) distri- bution, habitat use and foraging behaviour of this group are not well understood. Sooty shearwaters Ardenna grisea are among the world’s most numerous pelagic seabirds. -
University of California, San Diego
UNIVERSITY OF CALIFORNIA, SAN DIEGO Petrogenesis of Intraplate Lavas from Isolated Volcanoes in the Pacific: Implications for the Origin of the Enriched Mantle Source of OIB A dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Earth Sciences by Liyan Tian Committee in charge: Professor Paterno Castillo, Chair Professor David Hilton Professor James Hawkins Professor Mark Thiemens Professor Peter Lonsdale 2011 Copyright Liyan Tian, 2011 All rights reserved. The Dissertation of Liyan Tian is approved, and it is acceptable in quality and form for publication on microfilm and electronically: Chair University of California, San Diego 2011 iii This dissertation is dedicated to my parents, You Tian and Xiufen Jiang, who taught me to value education. iv TABLE OF CONTENTS SIGNATURE PAGE………………………………………………………………….iii DEDICATION………………………………………………………………………...iv TABLE OF CONTENTS……………………………………………………………...v LIST OF FIGURES………………………………………………………………….vii LIST OF TABLES…………………………………………………………………..viii ACKNOWLEDGEMENTS…………………………………………………………..ix VITA AND PUBLICATIONS………………………………………………………..xii ABSTRACT………………………………………………………………………….xv CHAPTER 1: Introduction…………………………………………………………….1 1.1. Scientific background and objectives of this dissertation………………………...1 1.2. Contents of the dissertation……………………………………………………….4 1.2.1. Chapter 2………………………………………………………………………..4 1.2.2. Chapter 3 and 4…………………………………………………………………6 1.2.3. Chapter 5………………………………………………………………………..7 1.3. Conclusions……………………………………………………………………….8 References……………………………………………………………………………12 -
Tinamiformes – Falconiformes
LIST OF THE 2,008 BIRD SPECIES (WITH SCIENTIFIC AND ENGLISH NAMES) KNOWN FROM THE A.O.U. CHECK-LIST AREA. Notes: "(A)" = accidental/casualin A.O.U. area; "(H)" -- recordedin A.O.U. area only from Hawaii; "(I)" = introducedinto A.O.U. area; "(N)" = has not bred in A.O.U. area but occursregularly as nonbreedingvisitor; "?" precedingname = extinct. TINAMIFORMES TINAMIDAE Tinamus major Great Tinamou. Nothocercusbonapartei Highland Tinamou. Crypturellus soui Little Tinamou. Crypturelluscinnamomeus Thicket Tinamou. Crypturellusboucardi Slaty-breastedTinamou. Crypturellus kerriae Choco Tinamou. GAVIIFORMES GAVIIDAE Gavia stellata Red-throated Loon. Gavia arctica Arctic Loon. Gavia pacifica Pacific Loon. Gavia immer Common Loon. Gavia adamsii Yellow-billed Loon. PODICIPEDIFORMES PODICIPEDIDAE Tachybaptusdominicus Least Grebe. Podilymbuspodiceps Pied-billed Grebe. ?Podilymbusgigas Atitlan Grebe. Podicepsauritus Horned Grebe. Podicepsgrisegena Red-neckedGrebe. Podicepsnigricollis Eared Grebe. Aechmophorusoccidentalis Western Grebe. Aechmophorusclarkii Clark's Grebe. PROCELLARIIFORMES DIOMEDEIDAE Thalassarchechlororhynchos Yellow-nosed Albatross. (A) Thalassarchecauta Shy Albatross.(A) Thalassarchemelanophris Black-browed Albatross. (A) Phoebetriapalpebrata Light-mantled Albatross. (A) Diomedea exulans WanderingAlbatross. (A) Phoebastriaimmutabilis Laysan Albatross. Phoebastrianigripes Black-lootedAlbatross. Phoebastriaalbatrus Short-tailedAlbatross. (N) PROCELLARIIDAE Fulmarus glacialis Northern Fulmar. Pterodroma neglecta KermadecPetrel. (A) Pterodroma -
Chick Growth and Development of the Short-Tailed Shearwater Puffinus Tenuirostris in Tasmania
山 階 鳥 研 報(J. Yamashina Inst. Ornith.),21:193-207,1989 Chick Growth and Development of the Short-tailed Shearwater Puffinus tenuirostris in Tasmania Nariko Oka* Abstract Chick growth of the short-tailed shearwater Puffinus tenuirostris, in a colony in Southern Tasmania was studied from mid January until the end of April 1988. Hatching took place between 10 and 25 January, with the peak occuring on 18 and 19 January. Fledging success was 35%. Mortality was concentrated in the middle of the nestling period and its main cause was predation by poachers and feral cats. Emergence from burrows began, on average, on the 88.7th night (±2.8SD) after hatching, which cor- responded to 13.9 April (±2.5SD). After consecutive emergence for 8.8 days(±3.5SD), they fledged on the 97.1th day (±3.3SD) after hatching, with the peak occurring between April 23 and 29. Hatched chicks, on average, had: 10% the body weight, 40% the tarsus length and 50% the bill (exposed culmen) length of adults and attained adult sizes during the middle of the nestling period. Chicks attained the body weight of about 15% heavier than the average adult, however, they lost 25 % of the peak body weight over the last three weeks and fledged at the mean body weight 13% lighter than the average adult. As com- pared with the early growth of their bony organs and body weight, their feather develop- ment was delayed. Tails began to sprout at 45.5 days (±2.6SD) after hatching and outer primaries sprouted at 34.2 days (±2.5SD) after hatching. -
Special Issue3.7 MB
Volume Eleven Conservation Science 2016 Western Australia Review and synthesis of knowledge of insular ecology, with emphasis on the islands of Western Australia IAN ABBOTT and ALLAN WILLS i TABLE OF CONTENTS Page ABSTRACT 1 INTRODUCTION 2 METHODS 17 Data sources 17 Personal knowledge 17 Assumptions 17 Nomenclatural conventions 17 PRELIMINARY 18 Concepts and definitions 18 Island nomenclature 18 Scope 20 INSULAR FEATURES AND THE ISLAND SYNDROME 20 Physical description 20 Biological description 23 Reduced species richness 23 Occurrence of endemic species or subspecies 23 Occurrence of unique ecosystems 27 Species characteristic of WA islands 27 Hyperabundance 30 Habitat changes 31 Behavioural changes 32 Morphological changes 33 Changes in niches 35 Genetic changes 35 CONCEPTUAL FRAMEWORK 36 Degree of exposure to wave action and salt spray 36 Normal exposure 36 Extreme exposure and tidal surge 40 Substrate 41 Topographic variation 42 Maximum elevation 43 Climate 44 Number and extent of vegetation and other types of habitat present 45 Degree of isolation from the nearest source area 49 History: Time since separation (or formation) 52 Planar area 54 Presence of breeding seals, seabirds, and turtles 59 Presence of Indigenous people 60 Activities of Europeans 63 Sampling completeness and comparability 81 Ecological interactions 83 Coups de foudres 94 LINKAGES BETWEEN THE 15 FACTORS 94 ii THE TRANSITION FROM MAINLAND TO ISLAND: KNOWNS; KNOWN UNKNOWNS; AND UNKNOWN UNKNOWNS 96 SPECIES TURNOVER 99 Landbird species 100 Seabird species 108 Waterbird -
Brachyura of the Pacific Coast of America Brachyrhyncha: Portunidae
n\oo ALLAN HANCOCK MONOGRAPHS IN MARINE BIOLOGY NUMBER 1 BRACHYURA OF THE PACIFIC COAST OF AMERICA BRACHYRHYNCHA: PORTUNIDAE BY JOHN S. GARTH AND W. STEPHENSON LOS ANGELES, CALIFORNIA PRINTED FOR THE ALLAN HANCOCK FOUNDATION UNIVERSITY OF SOUTHERN CALIFORNIA 1966 Kff' ALLAN HANCOCK MONOGRAPHS IN MARINE BIOLOGY NUMBER 1 BRACHYURA OF THE PACIFIC COAST OF AMERICA BRACHYRHYNCHA: PORTUNIDAE BY JOHN S. GARTH Allan Hancock Foundation and Department of Biological Sciences University of Southern California Los Angeles, California AND W. STEPHENSON Department of Zoology Ij nivcrsity of Queensland Brisbane, Australia I .OS ANGELES, CALIFORNIA PRINTED FOR THE ALLAN HANCOCK FOUNDATION UNIVERSITY OF SOUTHERN CALIFORNIA 1966 ALLAN HANCOCK MONOGRAPHS IN MARINE BIOLOGY NUMBER 1 ISSUED: APRIL 29, 1966 PRICE: $4.50 THE ALLAN HANCOCK FOUNDATION UNIVERSITY OF SOUTHERN CALIFORNIA Los ANGELES, CALIFORNIA TABLE OF CONTENTS General Discussion 1 Introduction 1 Source of Materials 2 Acknowledgment 2 Systematic Discussion 3 Method of Treatment 3 Historical Review 3 Analogous Atlantic Species 4 Explanation of Terms 8 Color Notes 9 Abbreviations 9 Family Portunidae 9 Subfamily Macropipinae 12 Genus Ovalipes 12 Ovalipes punctatus (de Haan) 12 Subfamily Portuninae 14 Genus Portunus 15 Portunus acuminatus (Stimpson) 17 Portunus angustus Rathbun 19 Portunus asper (A. Milne Edwards) 19 Portunus brevimanus (Faxon) 23 Portunus iridescens (Rathbun) 26 Portunus guaymasensis n. sp 29 Portunus stanfordi Rathbun 31 Portunus xantusii (Stimpson) 31 Portunus xantusii xantusii (Stimpson) 32 Portunus xantusii minimus (Rathbun) 35 Portunus xantusii affinis (Faxon) 38 Portunus tuberculatus (Stimpson) 40 Genus Callinectes 42 Callinectes arcuatus Ordway 43 Callinectes bellicosus (Stimpson) 47 Callinectes toxotes Ordway 50 Genus Arenaeus 52 Arenaeus mexicanus (Gerstaecker) 53 Genus Cronius 56 Cronius ruber (Lamarck) 57 Subfamily Podophthalminae 62 Genus Euphylax 63 Euphylax dovii Stimpson 64 Euphylax robustus A. -
Featured Photo: Notes on Plumage Maturation in the Red-Tailed Tropicbird
FEATURED PHOTO NOTES ON PLUMAGE MATURATION IN THE RED-TAILED TROPICBIRD RON LEVALLEY, Mad River Biologists, 920 Samoa Blvd., Suite 210, Arcata, Cali- fornia 95521; [email protected] PETER PYLE, The Institute for Bird Populations, P. O. Box 1346, Point Reyes Sta- tion, California 94956; [email protected] The Red-tailed Tropicbird (Phaethon rubricauda) is the most pelagic of the three species of tropicbirds. It ranges throughout the tropical Pacific and Indian oceans, nest- ing on islands. Young birds fledge alone, possibly with some postfledging parental care (Ainley et al. 1986), and most do not return to land for at least two years. During that time they wander, usually as single birds, well away from the sight of most observers. Most individuals return to breed at an age of 2–7 years. Although breeding at an age as young as 9 months, in a “near-adult like plumage,” has been reported (Schreiber and Schreiber 1993), we question this and wonder if the bird was older than suspected when banded the year before (see below). The majority of birds return by the age of 4 years, but those that reportedly return to breeding islands at 2 years of age (presumably in second basic plumage) are in almost full adult plumage (Schreiber and Schreiber 1993), and little is known about the species’ predefinitive molts and plumages. This uncertainty is compounded by year-round breeding in many populations, meaning that molts and plumages may not follow regular, season-based cycles at the population level. Individuals may undergo prebasic molts at intervals of less than one year (e.g., if a breeding attempt failed) or more than one year (e.g., if a breeding attempt was prolonged or skipped). -
Ii \ T MEXICAN GRASSES in the UNITED STATES NATIONAL
■ . ~+j-,r?7-w- - i i - . \ t MEXICAN GRASSES IN THE UNITED STATES NATIONAL HERBARIUM. By A. S, Hitchcock INTRODUCTION. The following list of grasses, based entirely upon specimens in the United States National Herbarium, is a preliminary paper, in which the scattered data upon Mexican grasses have been brought together and arranged in a convenient form. The species included have been accepted, for the most part, in their traditional sense. It has been impracticable to examine the types of many of the earlier described species since these specimens are located in European herbaria. For this reason the synonymy has been confined mostly to those names that could be fixed by an examination of American types, or concerning the application of which there was little doubt. The largest number of unidentified names are found in Fournier's work on Mexican grasses.1 This results from the incomplete or unsatis- factory descriptions and from the fact that the specimens cited under a given species either may not agree with the diagnosis, or may belong to two or more species, at least in different herbaria. An examination of the original specimens will undoubtedly lead to the identification of the greater part of these names. There are several specimens that have been omitted from the list because they have not been identified and are apparently unde- scribed species. They belong to genera, however, that are much in need of critical revision and further study of them is deferred for the present. In subsequent articles it is hoped to work out the classifi- cation of the tropical American grasses upon a type basis KEY TO THE GENEBA. -
ATOLL RESEARCH BULLETIN NO. 251 BIOGEOGRAPHY of the PUERTO RICAN BANK by Harold Heatwole, Richard Levins and Michael D. Byer
ATOLL RESEARCH BULLETIN NO. 251 BIOGEOGRAPHY OF THE PUERTO RICAN BANK by Harold Heatwole, Richard Levins and Michael D. Byer Issued by THE SMITHSONIAN INSTITUTION Washington, D. C., U.S.A. July 1981 VIRGIN ISLANDS CULEBRA PUERTO RlCO Fig. 1. Map of the Puerto Rican Island Shelf. Rectangles A - E indicate boundaries of maps presented in more detail in Appendix I. 1. Cayo Santiago, 2. Cayo Batata, 3. Cayo de Afuera, 4. Cayo de Tierra, 5. Cardona Key, 6. Protestant Key, 7. Green Key (st. ~roix), 8. Caiia Azul ATOLL RESEARCH BULLETIN 251 ERRATUM The following caption should be inserted for figure 7: Fig. 7. Temperature in and near a small clump of vegetation on Cayo Ahogado. Dots: 5 cm deep in soil under clump. Circles: 1 cm deep in soil under clump. Triangles: Soil surface under clump. Squares: Surface of vegetation. X's: Air at center of clump. Broken line indicates intervals of more than one hour between measurements. BIOGEOGRAPHY OF THE PUERTO RICAN BANK by Harold Heatwolel, Richard Levins2 and Michael D. Byer3 INTRODUCTION There has been a recent surge of interest in the biogeography of archipelagoes owing to a reinterpretation of classical concepts of evolution of insular populations, factors controlling numbers of species on islands, and the dynamics of inter-island dispersal. The literature on these subjects is rapidly accumulating; general reviews are presented by Mayr (1963) , and Baker and Stebbins (1965) . Carlquist (1965, 1974), Preston (1962 a, b), ~ac~rthurand Wilson (1963, 1967) , MacArthur et al. (1973) , Hamilton and Rubinoff (1963, 1967), Hamilton et al. (1963) , Crowell (19641, Johnson (1975) , Whitehead and Jones (1969), Simberloff (1969, 19701, Simberloff and Wilson (1969), Wilson and Taylor (19671, Carson (1970), Heatwole and Levins (1973) , Abbott (1974) , Johnson and Raven (1973) and Lynch and Johnson (1974), have provided major impetuses through theoretical and/ or general papers on numbers of species on islands and the dynamics of insular biogeography and evolution. -
Kaitiakitanga O Kā Tītī Ll
.DLWLDNLWDQJDR.Ɨ7ƯWƯOO A survey of a muttonbirding in the 2006 season Corey Bregg, Theresa Downs and Henrik Moller A report to Rakiura MƗori tƯtƯ harvesters University of Otago Year 2008 University of Otago Department of Zoology P.O. Box 56, Dunedin New Zealand WLM Report Number: 218 Kaitiakitanga o k Tt II A survey of a muttonbirding in the 2006 season A report to Rakiura Mori tt harvesters By Corey Bragg, Theresa Downs & Henrik Moller K Rakahau o Te Ao Troa - Centre for the Study of Agriculture Food & Environment Te Whare Wnanga o Otago - University of Otago PO Box 56, Dunedin University of Otago Wildlife Management Report No. 218 November 2008 Executive Summary This report summarises the results of a survey of 36 randomly-selected Rakiura Mori tt harvesters (“muttonbirders”). The survey was undertaken after the 2006 birding season, and consisted of 53 questions concerning tt ecology and harvest practices, the value or otherwise of research and potential management responses to ongoing declines in tt numbers. Responses were gathered during interviews, either in person or over the phone, or via a written questionnaire where this was not possible. The survey follows a similar one conducted after the 2001 season. It asked many of the same questions as the 2001 survey, so that a picture of long-term trends in birding can emerge. However, the emphasis of the 2006 survey was shifted slightly, to: (a) provide a complete survey of birders that went to the islands in 2006, and thus a snapshot of the birding community, (b) assess the birders’ views on potential management responses to falling tt abundance, and (c) predict the number of birders that might leave birding if tt numbers fell or increased in future.