Japan in Winter January 13–25, 2018
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Proposal 2017-C-15 Below)
AOS Classification Committee – North and Middle America Proposal Set 2017-C 15 March 2017 No. Page Title 01 02 Revise the linear sequence of genera in Fringillidae, and transfer Serinus mozambicus to Crithagra 02 09 Split Brown Creeper (Certhia americana) into two species 03 16 Transfer Violet-bellied Hummingbird from Damophila to Juliamyia 04 18 Elevate Colaptes auratus mexicanoides to species rank 05 23 Split Nashville Warbler (Oreothlypis ruficapilla) into two species 06 26 Adopt new English names for Melozone biarcuata and Melozone cabanisi 07 29 Lump Thayer’s Gull (Larus thayeri) with Iceland Gull (Larus glaucoides) 08 43 Change the spelling of the English names of Le Conte’s Thrasher (Toxostoma lecontei) and Le Conte’s Sparrow (Ammodramus leconteii) 09 46 Add Common Scoter (Melanitta nigra) to the Main List 10 49 Add Blyth’s Reed Warbler (Acrocephalus dumetorum) to the Main List 11 52 Add Chatham Albatross (Thalassarche eremita) to the Main List 12 55 Add Red-legged Honeycreeper (Cyanerpes cyaneus) to the U.S. list 13 57 Add nine species recorded from Greenland to the Main List 14 68 Split Bell’s Vireo (Vireo bellii) into two species 1 2017-C-1 N&MA Classification Committee pp. 658-679 Revise the linear sequence of genera in Fringillidae, and transfer Serinus mozambicus to Crithagra Background: In the past decade, several phylogenetic papers have elucidated relationships within the Fringillidae (Arnaiz-Villena et al. 2007, 2008, Nguembock et al. 2009, Lerner et al. 2011, Zuccon et al. 2012). NACC already has taken a series of actions (reviewed below) based on this research. -
Disaggregation of Bird Families Listed on Cms Appendix Ii
Convention on the Conservation of Migratory Species of Wild Animals 2nd Meeting of the Sessional Committee of the CMS Scientific Council (ScC-SC2) Bonn, Germany, 10 – 14 July 2017 UNEP/CMS/ScC-SC2/Inf.3 DISAGGREGATION OF BIRD FAMILIES LISTED ON CMS APPENDIX II (Prepared by the Appointed Councillors for Birds) Summary: The first meeting of the Sessional Committee of the Scientific Council identified the adoption of a new standard reference for avian taxonomy as an opportunity to disaggregate the higher-level taxa listed on Appendix II and to identify those that are considered to be migratory species and that have an unfavourable conservation status. The current paper presents an initial analysis of the higher-level disaggregation using the Handbook of the Birds of the World/BirdLife International Illustrated Checklist of the Birds of the World Volumes 1 and 2 taxonomy, and identifies the challenges in completing the analysis to identify all of the migratory species and the corresponding Range States. The document has been prepared by the COP Appointed Scientific Councilors for Birds. This is a supplementary paper to COP document UNEP/CMS/COP12/Doc.25.3 on Taxonomy and Nomenclature UNEP/CMS/ScC-Sc2/Inf.3 DISAGGREGATION OF BIRD FAMILIES LISTED ON CMS APPENDIX II 1. Through Resolution 11.19, the Conference of Parties adopted as the standard reference for bird taxonomy and nomenclature for Non-Passerine species the Handbook of the Birds of the World/BirdLife International Illustrated Checklist of the Birds of the World, Volume 1: Non-Passerines, by Josep del Hoyo and Nigel J. Collar (2014); 2. -
Natural History of Japanese Birds
Natural History of Japanese Birds Hiroyoshi Higuchi English text translated by Reiko Kurosawa HEIBONSHA 1 Copyright © 2014 by Hiroyoshi Higuchi, Reiko Kurosawa Typeset and designed by: Washisu Design Office Printed in Japan Heibonsha Limited, Publishers 3-29 Kanda Jimbocho, Chiyoda-ku Tokyo 101-0051 Japan All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means without permission in writing from the publisher. The English text can be downloaded from the following website for free. http://www.heibonsha.co.jp/ 2 CONTENTS Chapter 1 The natural environment and birds of Japan 6 Chapter 2 Representative birds of Japan 11 Chapter 3 Abundant varieties of forest birds and water birds 13 Chapter 4 Four seasons of the satoyama 17 Chapter 5 Active life of urban birds 20 Chapter 6 Interesting ecological behavior of birds 24 Chapter 7 Bird migration — from where to where 28 Chapter 8 The present state of Japanese birds and their future 34 3 Natural History of Japanese Birds Preface [BOOK p.3] Japan is a beautiful country. The hills and dales are covered “satoyama”. When horsetail shoots come out and violets and with rich forest green, the river waters run clear and the moun- cherry blossoms bloom in spring, birds begin to sing and get tain ranges in the distance look hazy purple, which perfectly ready for reproduction. Summer visitors also start arriving in fits a Japanese expression of “Sanshi-suimei (purple mountains Japan one after another from the tropical regions to brighten and clear waters)”, describing great natural beauty. -
GRUNDSTEN Japan 0102 2016
Birding Japan (M. Grundsten, Sweden) 2016 Japan, January 30th - February 14th 2016 Karuizawa – E Hokkaido – S Kyushu – Okinawa – Hachijo-jima Front cover Harlequin Duck Histrionicus histrionicus, common along eastern Hokkaido coasts. Photo: Måns Grundsten Participants Måns Grundsten ([email protected], compiler, most photos), Mattias Andersson, Mattias Gerdin, Sweden. Highlights • A shy Solitary Snipe in the main stream at Karuizawa. • Huge-billed Japanese Grosbeaks and a neat 'griseiventris' Eurasian Bullfinch at Karuizawa. • A single Rustic Bunting behind 7/Eleven at Karuizawa. • Amazing auks from the Oarai-Tomakomai ferry. Impressive numbers of Rhinoceros Auklet! • Parakeet Auklet fly-bys. • Blakiston's Fish Owl in orderly fashion at Rausu. • Displaying Black Scoters at Notsuke peninsula. • Majestic Steller's Sea Eagles in hundreds. • Winter gulls at Hokkaido. • Finding a vagrant Golden-crowned Sparrow at Kiritappu at the same feeders as Asian Rosy Finches. • No less than 48(!) Rock Sandpipers. • A lone immature Red-faced Cormorants on cliffs at Cape Nosappu. • A pair of Ural Owls on day roost at Kushiro. • Feeding Ryukyu Minivets at Lake Mi-ike. • Fifteen thousand plus cranes at Arasaki. • Unexpectedly productive Kogawa Dam – Long-billed Plover. • Saunders's Gulls at Yatsushiro. • Kin Ricefields on Okinawa, easy birding, lots of birds, odd-placed Tundra Bean Geese. • Okinawa Woodpecker and Rail within an hour close to Fushigawa Dam, Yanbaru. • Whistling Green Pigeon eating fruits in Ada Village. • Vocal Ryukyu Robins. • Good shorebird diversity in Naha. • Male Izu Thrush during a short break on Hachijo-jima. • Triple Albatrosses! • Bulwer's Petrel close to the ship. Planning the trip – Future aspects When planning a birding trip to Japan there is a lot of consideration to be made. -
Phylogeography of Finches and Sparrows
In: Animal Genetics ISBN: 978-1-60741-844-3 Editor: Leopold J. Rechi © 2009 Nova Science Publishers, Inc. Chapter 1 PHYLOGEOGRAPHY OF FINCHES AND SPARROWS Antonio Arnaiz-Villena*, Pablo Gomez-Prieto and Valentin Ruiz-del-Valle Department of Immunology, University Complutense, The Madrid Regional Blood Center, Madrid, Spain. ABSTRACT Fringillidae finches form a subfamily of songbirds (Passeriformes), which are presently distributed around the world. This subfamily includes canaries, goldfinches, greenfinches, rosefinches, and grosbeaks, among others. Molecular phylogenies obtained with mitochondrial DNA sequences show that these groups of finches are put together, but with some polytomies that have apparently evolved or radiated in parallel. The time of appearance on Earth of all studied groups is suggested to start after Middle Miocene Epoch, around 10 million years ago. Greenfinches (genus Carduelis) may have originated at Eurasian desert margins coming from Rhodopechys obsoleta (dessert finch) or an extinct pale plumage ancestor; it later acquired green plumage suitable for the greenfinch ecological niche, i.e.: woods. Multicolored Eurasian goldfinch (Carduelis carduelis) has a genetic extant ancestor, the green-feathered Carduelis citrinella (citril finch); this was thought to be a canary on phonotypical bases, but it is now included within goldfinches by our molecular genetics phylograms. Speciation events between citril finch and Eurasian goldfinch are related with the Mediterranean Messinian salinity crisis (5 million years ago). Linurgus olivaceus (oriole finch) is presently thriving in Equatorial Africa and was included in a separate genus (Linurgus) by itself on phenotypical bases. Our phylograms demonstrate that it is and old canary. Proposed genus Acanthis does not exist. Twite and linnet form a separate radiation from redpolls. -
Taimyr Gulls: Evidence for Pacific Winter Range, with Notes on Morphology and Breeding
Variation and difference in song between Western Bonelli’s Warbler and Eastern Bonelli’s Warbler and abundance. London. Jonsson, L 1992. Birds of Europe with North Africa and Hazevoet, C J & van der Schot, W E M 1986. Oostelijke the Middle East. London. Bergfluiters in Nederland in voorjaar van 1983. Dutch Occhiato, D 2007. Western and Eastern Bonelli’s War- Birding 8: 48-52. blers in the field. Birding World 20: 303-308. Helb, H-W, Bergmann, H-H & Martens, J 1982. Acoustic Reiser, O 1905. Materialien zu einer Ornis Balcanica 3. differences between populations of western and east- Wien. ern Bonelli’s Warblers (Phylloscopus bonelli, Sylvii- Sample, G 2003. Collins field guide to warbler songs dae). Experientia 38: 356-357. and calls of Britain and Europe. London. Helbig, A J, Seibold, I, Martens, J & Wink, M 1995. Sangster, G, Hazevoet, C J, van den Berg, A B, Roselaar, Genetic differentiation and phylogenetic relation- C S & Sluys, R, 1999. Dutch avifaunal list: species ships of Bonelli’s Warbler Phylloscopus bonelli and concepts, taxonomic instability, and taxonomic Green Warbler P nitidus. J Avian Biol 26: 139-153. changes in 1977-98. Ardea 87: 139-165. Kirwan, G M, Boyla, K A, Castell, P, Demirci, B, Ozen, Svensson, L, Grant, P J, Mullarney, K & Zetterström, D M, Welch, H & Marlow, T 2008. The birds of Turkey. 1999, 2009. Collins bird guide. First, second edition. London. London. Dick Groenendijk, Elzenstraat 14, 4043 PB Opheusden, Netherlands ([email protected]) Teus J C Luijendijk, Laan der zeven linden 50, 2645 GS Delfgauw, Netherlands ([email protected]) Taimyr Gulls: evidence for Pacific winter range, with notes on morphology and breeding Klaas van Dijk, Sergei Kharitonov, Holmer Vonk & Bart Ebbinge he Taimyr peninsula in the northern part of the Caspian Sea area, along the Arabian Sea to Tcentral Siberia, Russia, hosts a significant western India, and partly also along coasts in east- breeding population of gulls Larus that belong to ern Africa. -
Lhasa and the Tibetan Plateau Cumulative
Lhasa and the Tibetan Plateau Cumulative Bird List Column A: Total number of tours (out of 6) that the species was recorded Column B: Total number of days that the species was recorded on the 2016 tour Column C: Maximum daily count for that particular species on the 2016 tour Column D: H = Heard Only; (H) = Heard more than seen Globally threatened species as defined by BirdLife International (2004) Threatened birds of the world 2004 CD-Rom Cambridge, U.K. BirdLife International are identified as follows: EN = Endangered; VU = Vulnerable; NT = Near- threatened. A B C D 6 Greylag Goose 2 15 Anser anser 6 Bar-headed Goose 4 300 Anser indicus 3 Whooper Swan 1 2 Cygnus cygnus 1 Common Shelduck Tadorna tadorna 6 Ruddy Shelduck 8 700 Tadorna ferruginea 3 Gadwall 2 3 Anas strepera 1 Eurasian Wigeon Anas penelope 5 Mallard 2 8 Anas platyrhynchos 2 Eastern Spot-billed Duck Anas zonorhyncha 1 Indian or Eastern Spot-billed Duck Anas poecilorhynchos or A. zonorhyncha 1 Northern Shoveler Anas clypeata 1 Northern Pintail Anas acuta 1 Garganey 2 15 Anas querquedula 4 Eurasian Teal 2 50 Anas crecca 6 Red-crested Pochard 3 2000 Netta rufina 6 Common Pochard 2 200 Aythya ferina 3 Ferruginous Duck NT 1 8 Aythya nyroca 6 Tufted Duck 2 200 Aythya fuligula 5 Common Goldeneye 2 11 Bucephala clangula 4 Common Merganser 3 51 Mergus merganser 5 Chinese Grouse NT 2 1 Tetrastes sewerzowi 4 Verreaux's Monal-Partridge 1 1 H Tetraophasis obscurus 5 Tibetan Snowcock 1 5 H Tetraogallus tibetanus 4 Przevalski's Partridge 1 1 Alectoris magna 1 Daurian Partridge Perdix dauurica 6 Tibetan Partridge 2 11 Perdix hodgsoniae ________________________________________________________________________________________________________ WINGS ● 1643 N. -
Satoyama Landscapes and Their Change in a River Basin Context: Lessons for Sustainability
Issues in Social Science ISSN 2329-521X 2016, Vol. 5, No. 1 Satoyama Landscapes and Their Change in A River Basin context: Lessons for Sustainability Shamik Chakraborty (Corresponding author) Institute for the Advanced Study of Sustainability (IAS), United Nations University 5-53-70 Jingumae, Shibuya-ku, Tokyo, 150-8925, Japan Tel: 81-3-5467-1212 E-mail: [email protected] Abhik Chakraborty Center for Tourism Research, Wakayama University 930 Sakaedani, Wakayama city, Wakayama, 649-8441, Japan Tel: 81-73-456-7025 Email: [email protected] Received: March 10, 2017 Accepted: April 6, 2017 Published: June 14, 2017 doi:10.5296/iss.v5i1.10892 URL: http://dx.doi.org/10.5296/iss.v5i1.10892 Abstract 'Satoyama' denotes a mosaic of different landscape-types that has sustained agrarian societies for millennia in Japan. These landscapes have undergone degradation during the past few decades. While satoyama is a consistently referred term in landscape management in Japan, little attention is given to how such landscapes undergo change in large spatial units such as river basins. This study, based on documents and interviews, reviews how watershed level changes affect the functioning of such socioecological systems in the Kuma River Basin in Kyushu. Watershed properties of the Kuma River Basin changed during pre-modern and modern times and each phase left a lasting legacy on the landscape. The article analyzes how ecological connectivity became fragmented by identifying changes in ecosystem services, and concludes that while socio-ecological landscapes have a long history of human use; the human component cannot outgrow the fundamental biophysical processes that maintain ecosystem services and system resilience; these systems can undergo swift and irreversible degradation when ecological connectivity is fragmented. -
Flood Loss Model Model
GIROJ FloodGIROJ Loss Flood Loss Model Model General Insurance Rating Organization of Japan 2 Overview of Our Flood Loss Model GIROJ flood loss model includes three sub-models. Floods Modelling Estimate the loss using a flood simulation for calculating Riverine flooding*1 flooded areas and flood levels Less frequent (River Flood Engineering Model) and large- scale disasters Estimate the loss using a storm surge flood simulation for Storm surge*2 calculating flooded areas and flood levels (Storm Surge Flood Engineering Model) Estimate the loss using a statistical method for estimating the Ordinarily Other precipitation probability distribution of the number of affected buildings and occurring disasters related events loss ratio (Statistical Flood Model) *1 Floods that occur when water overflows a river bank or a river bank is breached. *2 Floods that occur when water overflows a bank or a bank is breached due to an approaching typhoon or large low-pressure system and a resulting rise in sea level in coastal region. 3 Overview of River Flood Engineering Model 1. Estimate Flooded Areas and Flood Levels Set rainfall data Flood simulation Calculate flooded areas and flood levels 2. Estimate Losses Calculate the loss ratio for each district per town Estimate losses 4 River Flood Engineering Model: Estimate targets Estimate targets are 109 Class A rivers. 【Hokkaido region】 Teshio River, Shokotsu River, Yubetsu River, Tokoro River, 【Hokuriku region】 Abashiri River, Rumoi River, Arakawa River, Agano River, Ishikari River, Shiribetsu River, Shinano -
Egg Recognition in Cinereous Tits (Parus Cinereus): Eggshell Spots Matter Jianping Liu1 , Canchao Yang1 , Jiangping Yu2,3 , Haitao Wang2,4 and Wei Liang1*
Liu et al. Avian Res (2019) 10:37 https://doi.org/10.1186/s40657-019-0178-1 Avian Research RESEARCH Open Access Egg recognition in Cinereous Tits (Parus cinereus): eggshell spots matter Jianping Liu1 , Canchao Yang1 , Jiangping Yu2,3 , Haitao Wang2,4 and Wei Liang1* Abstract Background: Brood parasitic birds such as cuckoos (Cuculus spp.) can reduce their host’s reproductive success. Such selection pressure on the hosts has driven the evolution of defense behaviors such as egg rejection against cuckoo parasitism. Studies have shown that Cinereous Tits (Parus cinereus) in China have a good ability for recognizing foreign eggs. However, it is unclear whether egg spots play a role in egg recognition. The aims of our study were to inves- tigate the egg recognition ability of two Cinereous Tit populations in China and to explore the role of spots in egg recognition. Methods: To test the efect of eggshell spots on egg recognition, pure white eggs of the White-rumped Munia (Lon- chura striata) and eggs of White-rumped Munia painted with red brown spots were used to simulate experimental parasitism. Results: Egg experiments showed that Cinereous Tits rejected 51.5% of pure white eggs of the White-rumped Munia, but only 14.3% of spotted eggs of the White-rumped Munia. There was a signifcant diference in egg recognition and rejection rate between the two egg types. Conclusions: We conclude that eggshell spots on Cinereous Tit eggs had a signaling function and may be essential to tits for recognizing and rejecting parasitic eggs. Keywords: Brood parasitism, Egg recognition, Egg rejection, Eggshell spots, Parus cinereus Background egg rejection by hosts, many parasitic birds evolve coun- Te mutual adaptations and counter-defense strategies ter-adaptations to overcome the hosts’ defenses by laying between brood parasitic birds such as cuckoos (Cuculus mimicking (Brooke and Davies 1988; Avilés et al. -
The Geobiology and Ecology of Metasequoia
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/37160841 The Geobiology and Ecology of Metasequoia. Article · January 2005 Source: OAI CITATIONS READS 11 457 3 authors: Ben LePage Christopher J. Williams Pacific Gas and Electric Company Franklin and Marshall College 107 PUBLICATIONS 1,864 CITATIONS 55 PUBLICATIONS 1,463 CITATIONS SEE PROFILE SEE PROFILE Hong Yang Massey University 54 PUBLICATIONS 992 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Conifer (Pinaceae and Cupressaceae (Taxodiaceae)) systematics and phylogeny View project All content following this page was uploaded by Ben LePage on 24 September 2014. The user has requested enhancement of the downloaded file. Chapter 1 The Evolution and Biogeographic History of Metasequoia BEN A. LePAGE1, HONG YANG2 and MIDORI MATSUMOTO3 1URS Corporation, 335 Commerce Drive, Suite 300, Fort Washington, Pennsylvania, 19034, USA; 2Department of Science and Technology, Bryant University, 1150 Douglas Pike, Smithfield, Rhode Island, 02917, USA; 3Department of Earth Sciences, Chiba University, Yayoi-cho 133, Inage-ku, Chiba 263, Japan. 1. Introduction .............................................................. 4 2. Taxonomy ............................................................... 6 3. Morphological Stasis and Genetic Variation ................................. 8 4. Distribution of Metasequoia Glyptostroboides ............................... 10 5. Phytogeography ......................................................... -
Alarm Calls Evoke a Visual Search Image of a Predator in Birds
Alarm calls evoke a visual search image of a predator in birds Toshitaka N. Suzukia,b,1 aCenter for Ecological Research, Kyoto University, Otsu, 520-2113 Shiga, Japan; and bDepartment of Evolutionary Studies of Biosystems, Graduate University for Advanced Studies, Hayama, 240-0193 Kanagawa, Japan Edited by Asif A. Ghazanfar, Princeton University, Princeton, NJ, and accepted by Editorial Board Member Marlene Behrmann December 29, 2017 (received for review October 30, 2017) One of the core features of human speech is that words cause including avian and mammalian predators (13) (Fig. 1B). In re- listeners to retrieve corresponding visual mental images. How- sponse to these general alarm calls, receivers approach the sound ever, whether vocalizations similarly evoke mental images in source and scan the surroundings (17), but do not show any animal communication systems is surprisingly unknown. Japanese specific behaviors to defend themselves against snakes (15, 16). tits (Parus minor) produce specific alarm calls when and only when Based on these previous studies, I hypothesized that snake- encountering a predatory snake. Here, I show that simply hearing specific alarm calls evoke a visual search image of a snake in tits. these calls causes tits to become more visually perceptive to ob- A key prediction of this hypothesis is that receivers are primed to jects resembling snakes. During playback of snake-specific alarm detect snakes when hearing snake-specific alarm calls. However, calls, tits approach a wooden stick being moved in a snake-like to provide evidence for visual mental imagery, individuals should fashion. However, tits do not respond to the same stick when be primed to detect snakes even in the absence of real snakes, ’ hearing other call types or if the stick s movement is dissimilar since simply seeing a snake may directly trigger its mental image to that of a snake.