Birds of Conservation Concern 3 the Population Status of Birds in the United Kingdom, Channel Islands and Isle of Man Mark A
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444 Yellowhammer Put Your Logo Here
Javier Blasco-Zumeta & Gerd-Michael Heinze Sponsor is needed. Write your name here 444 Yellowhammer Put your logo here Yellowhammer. Winter. Adult. Male (04-XI) Yellowhammer. Spring. Pattern of upperparts and YELLOWHAMMER (Emberiza citri- head: top male (Photo: nella) Ottenby Bird Observa- tory); bottom female IDENTIFICATION (Photo: Ottenby Bird Observatory). 14-18 cm. Breeding male with yellow head; reddish upperparts, brown streaked; chestnut- reddish rump and uppertail coverts, unstreaked; bluish bill; in winter similar to female. Female more brownish and streaked than male. Yellowhammer. Juvenile. Pattern of head (Photo: Ondrej Kauzal) and up- perparts (Photo: Alejan- dro Corregidor). SIMILAR SPECIES Male in breeding plumage unmistakable. Fe- Yellowhammer. Win- male similar to female Cirl Bunting which ter. Pattern of upper- has grey-olive rump and lacks pale patch on parts and head: top nape. Female Ortolan Bunting has brown rump male; bottom female. and grey-buff underparts. Juveniles Yellowham- mer are unmistakable due to their chestnut rump. http://blascozumeta.com Write your website here Page 1 Javier Blasco-Zumeta & Gerd-Michael Heinze Sponsor is needed. Write your name here 444 Yellowhammer Put your logo here Yellowham- mer. Spring. Sexing. Pat- tern of head: top male (Photo: Ot- tenby Bird Observa- tory); bot- tom female (Photo: Ot- tenby Bird Observa- Cirl Bunting. Female tory). Yellowhammer. Spring. Sexing. Pattern of breast: Ortolan Bunting. 1st year. left male (Photo: Reinhard Vohwinkel); right female (Photo: Reinhard Vohwinkel). SEXING In breeding plumage, male with head and under- parts deep yellow. Female with head and under- parts brownish. After postbreeding/postjuvenile moults, adult male with crown feathers yellow on more than half length without a dark shaft streak. -
Condition of Designated Sites
Scottish Natural Heritage Condition of Designated Sites Contents Chapter Page Summary ii Condition of Designated Sites (Progress to March 2010) Site Condition Monitoring 1 Purpose of SCM 1 Sites covered by SCM 1 How is SCM implemented? 2 Assessment of condition 2 Activities and management measures in place 3 Summary results of the first cycle of SCM 3 Action taken following a finding of unfavourable status in the assessment 3 Natural features in Unfavourable condition – Scottish Government Targets 4 The 2010 Condition Target Achievement 4 Amphibians and Reptiles 6 Birds 10 Freshwater Fauna 18 Invertebrates 24 Mammals 30 Non-vascular Plants 36 Vascular Plants 42 Marine Habitats 48 Coastal 54 Machair 60 Fen, Marsh and Swamp 66 Lowland Grassland 72 Lowland Heath 78 Lowland Raised Bog 82 Standing Waters 86 Rivers and Streams 92 Woodlands 96 Upland Bogs 102 Upland Fen, Marsh and Swamp 106 Upland Grassland 112 Upland Heathland 118 Upland Inland Rock 124 Montane Habitats 128 Earth Science 134 www.snh.gov.uk i Scottish Natural Heritage Summary Background Scotland has a rich and important diversity of biological and geological features. Many of these species populations, habitats or earth science features are nationally and/ or internationally important and there is a series of nature conservation designations at national (Sites of Special Scientific Interest (SSSI)), European (Special Area of Conservation (SAC) and Special Protection Area (SPA)) and international (Ramsar) levels which seek to protect the best examples. There are a total of 1881 designated sites in Scotland, although their boundaries sometimes overlap, which host a total of 5437 designated natural features. -
Scotland 2014 Outer Hebrides & the Highlands
Scotland 2014 Outer Hebrides & the Highlands 22 May – 7 June 2014 St Kilda Wren, Hirta, St Kilda, Scotland, 30 May 2014 (© Vincent van der Spek) Vincent van der Spek, July 2014 1 highlights Red Grouse (20), Ptarmigan (4-5), Black Grouse (5), American Wigeon (1), Long- tailed Duck (5), three divers in summer plumage: Great Northern (c. 25), Red- throated (dozens) and Black-throated (1), Slavonian Grebe (1), 10.000s of Gannets and 1000s of Fulmars, Red Kite (5), Osprey (2 different nests), White-tailed Eagle (8), Golden Eagle (1), Merlin (2), Corncrake (2), the common Arctic waders in breeding habitat, Dotterel (1), Pectoral Sandpiper (1), sum plum Red-necked Phalarope (2), Great Skua (c. 125), Glaucous Gull (1), Puffin (c. 20.000), Short- eared Owl (1), Rock Dove (many), St Kilda Wren (8), other ssp. from the British Isles (incl. Wren Dunnock and Song Thrush from the Hebrides), Ring Ouzel (4), Scottish Crossbill (9), Snow Bunting (2), Risso’s Dolphin (4), Otter (1). missed species Capercaillie, ‘Irish’ Dipper ssp. hibernicus, the hoped for passage of Long-tailed and Pomarine Skuas, Midgets. Ptarmigan, male, Cairn Gorm, Highlands, Scotland, 3 June 2014 (© Vincent van der Spek) 2 introduction Keete suggested Scotland as a holiday destination several times in the past, so after I dragged her to many tropical destinations instead it was about time we went to the northern part of the British Isles. And I was not to be disappointed! Scotland really is a beautiful place, with great people. Both on the isles, with its wild and sometimes desolate vibe and very friendly folks and in the highlands, there seemed to be a stunning view behind every stunning view. -
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. -
A Report of Brambling Fringilla Montifringilla from Mandala Road, Arunachal Pradesh Qupeleio De Souza
136 Indian BirDS VOL. 10 NO. 5 (PUBL. 2 NOVEMBER 2015) and the Middle East (Ali & Ripley 1986). However, observations of the Rosy Starling in the sub-Himalayan or Himalayan areas are very rare (please see distribution map in Grimmett et al. 2011: 404). Published bird checklists, relevant to the Doon Valley in particular (Pandey et al. 1994; Mohan 1996; Singh 2000), and for similar landscapes in the region (Sharma et al. 2003) have no record of the Rosy Starling. The bird is also not listed in the official checklist of birds published by the Uttarakhand Forest Department (Mohan & Sinha 2003). Hence, according to the best of my knowledge, this species has never been observed in Uttarakhand and this sighting is a new record for the state. Since only a single individual was seen of this otherwise highly gregarious bird, it is likely that the Rosy Starling I observed was a vagrant. Acknowledgements I am grateful to Mohammed Bashir for assistance in field, and Soumya Prasad for support. Photo: Raman Kumar References Ali, S., & Ripley, S. D., 1986. Handbook of the birds of India and Pakistan together with those of Bangladesh, Nepal, Bhutan and Sri Lanka. Cuckoo-shrikes to babaxes. 2nd (Hardback) ed. Delhi: (Sponsored by Bombay Natural History Society.) Oxford University Press. Vol. 5 of 10 vols. Pp. i–xvi, 1–278+2+8 ll. 126. Rosy Starling feeding on Mallotus sp. tree, Doon Valley. Champion, H. G., & Seth, S. K., 1968. A revised survey of the forest types of India. Government of India, Delhi. Grimmett, R., Inskipp, C., & Inskipp, T., 2011. -
Four Year Study Involving Wildlife Monitoring of Commercial SRC Plantations Planted on Arable Land and Arable Control Plots
Four year study involving wildlife monitoring of commercial SRC plantations planted on arable land and arable control plots DTI TECHNOLOGY PROGRAMME: NEW AND RENEWABLE ENERGY CONTRACT NUMBER B/U1/00627/00/00 URN NUMBER 04/961 PROJECT REPORT The DTI drives our ambition of ’prosperity for all' by working to create the best environment for business success in the UK. We help people and companies become more productive by promoting enterprise, innovation and creativity. We champion UK business at home and abroad. We invest heavily in world-class science and technology. We protect the rights of working people and consumers. And we stand up for fair and open markets in the UK, Europe and the world. ii ARBRE MONITORING - ECOLOGY OF SHORT ROTATION COPPICE B/U1/00627/REP DTI/PUB URN 04/961 Contractor The Game Conservancy Trust (GCT) Sub-Contractor The Central Science Laboratory (CSL) Prepared by M.D.Cunningham (GCT) J.D. Bishop (CSL) H.V.McKay (CSL) R.B.Sage (GCT) The work described in this report was carried out under contract as part of the DTI Technology Programme: New and Renewable Energy. The views and judgements expressed in this report are those of the contractor and do not necessarily reflect those of the DTI. First published 2004 © Crown Copyright 2004 ii i EXECUTIVE SUMMARY Introduction This project, funded by the Department of Trade and Industry (DTI) through Future Energy Solutions, was conducted over a four-year period starting in 2000. The project involved wildlife monitoring within Short Rotation Coppice (SRC) plots managed commercially for the project ARBRE (Arable Biomass Renewable Energy) throughout Yorkshire. -
Breeding Farmland Birds and the Role of Habitats Created Under Agri-Environment Schemes
Breeding farmland birds and the role of habitats created under agri-environment schemes Niamh M. McHugh Department of Life Sciences Imperial College London A thesis submitted for the degree of Doctor of Philosophy rd 23 of April, 2015 Abstract In this thesis, I aim to assess how farmland birds use insect-rich agri-environment scheme (AES) foraging habitats during the breeding season and how such birds might benefit from them. It is particularly focused on how the coverage and quality (measured by insect food levels and food accessibility) of AES habitats influence territory selection, foraging activities and breeding success. The thesis begins by explaining why farmland birds have declined, reviewing how AES may help reverse these trends, along with outlining why AES may fail to benefit breeding birds (Chapter one). I then investigated whether the addition of wildflowers to AES margins, boundary type, crop type, chick food availability or accessibility influenced the foraging activity of insectivores, mixed diet species and the passerine community in general (Chapter two). Next, I wanted to find out if territory selection by a declining farmland bird the yellowhammer Emberiza citronella related to the quantity of AES habitat available; models also accounted for chick food abundance, landscape diversity and nest site features (Chapter three). Subsequently I investigated how the availability of AES can affect chick diet and survival using the Eurasian tree sparrow Passer monatus as a focus species. I compared the abundance and diversity of tree sparrow chick food items between nest boxes with and without access to AES habitats aimed at foraging birds (Chapter four). -
Rejection Behavior by Common Cuckoo Hosts Towards Artificial Brood Parasite Eggs
REJECTION BEHAVIOR BY COMMON CUCKOO HOSTS TOWARDS ARTIFICIAL BROOD PARASITE EGGS ARNE MOKSNES, EIVIN ROSKAFT, AND ANDERS T. BRAA Departmentof Zoology,University of Trondheim,N-7055 Dragvoll,Norway ABSTRACT.--Westudied the rejectionbehavior shown by differentNorwegian cuckoo hosts towardsartificial CommonCuckoo (Cuculus canorus) eggs. The hostswith the largestbills were graspejectors, those with medium-sizedbills were mostlypuncture ejectors, while those with the smallestbills generally desertedtheir nestswhen parasitizedexperimentally with an artificial egg. There were a few exceptionsto this general rule. Becausethe Common Cuckooand Brown-headedCowbird (Molothrus ater) lay eggsthat aresimilar in shape,volume, and eggshellthickness, and they parasitizenests of similarly sizedhost species,we support the punctureresistance hypothesis proposed to explain the adaptivevalue (or evolution)of strengthin cowbirdeggs. The primary assumptionand predictionof this hypothesisare that somehosts have bills too small to graspparasitic eggs and thereforemust puncture-eject them,and that smallerhosts do notadopt ejection behavior because of the heavycost involved in puncture-ejectingthe thick-shelledparasitic egg. We comparedour resultswith thosefor North AmericanBrown-headed Cowbird hosts and we found a significantlyhigher propor- tion of rejectersamong CommonCuckoo hosts with graspindices (i.e. bill length x bill breadth)of <200 mm2. Cuckoo hosts ejected parasitic eggs rather than acceptthem as cowbird hostsdid. Amongthe CommonCuckoo hosts, the costof acceptinga parasiticegg probably alwaysexceeds that of rejectionbecause cuckoo nestlings typically eject all hosteggs or nestlingsshortly after they hatch.Received 25 February1990, accepted 23 October1990. THEEGGS of many brood parasiteshave thick- nestseither by grasping the eggs or by punc- er shells than the eggs of other bird speciesof turing the eggs before removal. Rohwer and similar size (Lack 1968,Spaw and Rohwer 1987). -
Download Report
BTO Research Report 384 The London Bird Project Authors Dan Chamberlain, Su Gough, Howard Vaughan, Graham Appleton, Steve Freeman, Mike Toms, Juliet Vickery, David Noble A report to The Bridge House Estates Trust January 2005 © British Trust for Ornithology British Trust for Ornithology, The Nunnery, Thetford, Norfolk IP24 2PU Registered Charity No. 216652 British Trust for Ornithology The London Bird Project BTO Research Report No. 384 Dan Chamberlain, Su Gough, Howard Vaughan, Graham Appleton, Steve Freeman, Mike Toms, Juliet Vickery, David Noble Published in January 2005 by the British Trust for Ornithology The Nunnery, Thetford, Norfolk, IP24 2PU, UK Copyright © British Trust for Ornithology 2005 ISBN 1-904870-18-X All rights reserved. No part of this publication may be reproduced, stored in a retrieval system or transmitted, in any form, or by any means, electronic, mechanical, photocopying, recording or otherwise, without the prior permission of the publishers CONTENTS Page No. List of Tables .........................................................................................................................................3 List of Figures........................................................................................................................................5 List of Appendices.................................................................................................................................7 Executive Summary ..............................................................................................................................9 -
Breeding Nomadism and Site Tenacity in the Brambling Fringilla Montifringilla
Breeding nomadism and site tenacity in the Brambling Fringilla montifringilla Åke Lindström Lindström, A. 1987 : Breeding nomadism and site tenacity in the Brambling Fringilla montifringilla . -Ornis Fennica 64:50-56. Territory mapping in subalpine birch forest in Ammaraäs, Swedish Lapland, during 1963-1986 revealed that Brambling Fringilla montifringilla densities are highest in years with high densities of caterpillars of the geometrid moth Epirrita autumnata. The number of stationary males was positively correlated with the number of nests found in the area. Thus, the birds moving into the area do attempt to breed there. In 1983-1986, 999 Bramblings were trapped during the post-breeding period. The proportion of juveniles was significantly higher in years with Epirrita peak abundance. The data indicate that the density of breeding Bramblings in Ammarns depends on Epirrita . Ringing recoveries and the almost complete abscence of recaptures of birds ringed in Ammarnäs in earlier years show that both males and females normally change their breeding sites between years, i.e. they are nomadic. Breeding site fidelity may occur, however, since one male ringed in 1985 returned to Ammarnäs in 1986 . The mean wing lengths of adult females varied significantly between years (1983-1986). As only 60% of these birds could be properly aged it was not possible to discover whether the differencesbetween years were due to a varying proportion of older birds. Older females (+3y) were significantly larger in years with peak food abundance. The mean wing lengths in adult males did not differ significantly between years. The breeding site strategy of the Brambling is discussed in relation to a theoretical model of breeding nomadism. -
Loxia Scotica
Loxia scotica -- Hartert, 1904 ANIMALIA -- CHORDATA -- AVES -- PASSERIFORMES -- FRINGILLIDAE Common names: Scottish Crossbill; European Red List Assessment European Red List Status LC -- Least Concern, (IUCN version 3.1) Assessment Information Year published: 2015 Date assessed: 2015-03-31 Assessor(s): BirdLife International Reviewer(s): Symes, A. Compiler(s): Ashpole, J., Burfield, I., Ieronymidou, C., Pople, R., Wheatley, H. & Wright, L. Assessment Rationale European regional assessment: Least Concern (LC) EU27 regional assessment: Least Concern (LC) At both European and EU27 scales, although this species may have a small range it is not believed to approach the thresholds for Vulnerable under the range size criterion (Extent of Occurrence 10% in ten years or three generations, or with a specified population structure). The population trend is not known, but the population is not believed to be decreasing sufficiently rapidly to approach the thresholds under the population trend criterion (30% decline over ten years or three generations). For these reasons the species is evaluated as Least Concern within both Europe and the EU27. Occurrence Countries/Territories of Occurrence Native: United Kingdom Population The European population is estimated at 4,100-11,400 pairs, which equates to 8,200-22,800 mature individuals. The entire population is found in the EU27. For details of national estimates, see Supplementary PDF. Trend In Europe and the EU27 the population size trend is unknown. For details of national estimates, see Supplementary PDF. Habitats and Ecology This species breeds in lowland forests and stands of Scots pine (Pinus sylvestris), including open mature plantations and ancient relict forest trees. During the winter it is mostly found in larches (Larix) and in established plantations of lodgepole pine (Pinus contorta) and sitka spruce (Picea sitchensis) as well as well- spaced pine woodland with heather (Calluna) understorey. -
Federal Register/Vol. 85, No. 74/Thursday, April 16, 2020/Notices
21262 Federal Register / Vol. 85, No. 74 / Thursday, April 16, 2020 / Notices acquisition were not included in the 5275 Leesburg Pike, Falls Church, VA Comment (1): We received one calculation for TDC, the TDC limit would not 22041–3803; (703) 358–2376. comment from the Western Energy have exceeded amongst other items. SUPPLEMENTARY INFORMATION: Alliance, which requested that we Contact: Robert E. Mulderig, Deputy include European starling (Sturnus Assistant Secretary, Office of Public Housing What is the purpose of this notice? vulgaris) and house sparrow (Passer Investments, Office of Public and Indian Housing, Department of Housing and Urban The purpose of this notice is to domesticus) on the list of bird species Development, 451 Seventh Street SW, Room provide the public an updated list of not protected by the MBTA. 4130, Washington, DC 20410, telephone (202) ‘‘all nonnative, human-introduced bird Response: The draft list of nonnative, 402–4780. species to which the Migratory Bird human-introduced species was [FR Doc. 2020–08052 Filed 4–15–20; 8:45 am]‘ Treaty Act (16 U.S.C. 703 et seq.) does restricted to species belonging to biological families of migratory birds BILLING CODE 4210–67–P not apply,’’ as described in the MBTRA of 2004 (Division E, Title I, Sec. 143 of covered under any of the migratory bird the Consolidated Appropriations Act, treaties with Great Britain (for Canada), Mexico, Russia, or Japan. We excluded DEPARTMENT OF THE INTERIOR 2005; Pub. L. 108–447). The MBTRA states that ‘‘[a]s necessary, the Secretary species not occurring in biological Fish and Wildlife Service may update and publish the list of families included in the treaties from species exempted from protection of the the draft list.