Nest-Site Provision Experiment for Long-Eared Owls to Attempt To

Total Page:16

File Type:pdf, Size:1020Kb

Nest-Site Provision Experiment for Long-Eared Owls to Attempt To Notes Nest-site provision experiment for Long-eared Owls To attempt to improve the breeding success of Long-eared Owls Asio otus, artificial nest- sites were provided in an area where the owls were known to overwinter. The nests provided consisted of two types: old potato or apple-picker baskets made of willow, with the handles removed, and baskets of a similar shape made of wire-netting. Three willow baskets and six wire baskets were sited in November 1979, in a small Cambridgeshire wood of mixed deciduous trees, comprising mainly willow Salix, silver birch Betula, oak Quercus and hawthorn Crataegus. All the baskets were fixed to suitable trees at a height of approximately 5 m, and then each lined with sticks of various lengths and thicknesses to provide a firm base. 140. Long-eared Owl Asio otus on nest in willow basket provided as artificial nest-site, Cambridgeshire, May 1981 (D.J. Gamer) continued... 376 Notes 377 During the first year, 1980, none of the baskets was used, but in 1981 one of the willow baskets was occupied by a pair of Long-eared Owls (plate 140), which had a clutch of three eggs, of which two hatched, and two young fledged. Current literature states that Long-eared Owls nest in the same area each year, but not in the same nest. This is probably due to the fact that natural sites (e.g. old birds' nests and squirrels' dreys) are destroyed over winter and do not last for a further year. With this experiment using these more substantial nests, it is hoped that the same site will be used in succeeding years. D.J. GARNER 73 Needingworth Road, St Ives, Huntingdon, Cambridgeshire PE174JY Nightjar taking water in flight So far as I am aware, there are no published records of the Nightjar Caprimulgus europaeus taking water, but observations in Sudan suggest that water may be taken in flight. Just after sunset on 2nd November 1977, I saw a late migrant Nightjar leave some bushy vegetation bordering the Blue Nile near Khartoum and fly down to a few centimetres above the river; it then flew parallel to the bank and, as it passed me at 3-4m, lifted its tail and wings a little above the body level and dipped its head so that its bill scooped the water momentarily, rippling the surface, in a manner similar to that employed by hirundines or swifts Apus taking water on the wing; it continued over the water as though to repeat the action, but unfortunately passed behind some vegetation out of sight before doing so. Very few nightjars have been recorded taking water, presumably because exceptional conditions are required for such observations. All refer to water being taken in flight. Published reports include: the Golden Nightjar C. eximius in the Sudan (Ibis (1902): 1-33); the Egyptian Nightjar C. aegyptius in Turkestan (Dementiev & Gladkov, 1966, Birds of the Soviet Union, vol. 1); and the Allied Nightjar C. ajfinis of Pakistan and India (Ali & Ripley, 1970, Handbook of the Birds oj India and Pakistan, vol. 4). In addition, I have seen the Long-tailed Nightjar C. climacturus taking water in flight at Khartoum, although in a manner somewhat different from that described above. ANTONY PETTET Botany Department, University of Khartoum, Khartoum, Sudan Swift persistently attacking Starling On 7th September 1979, while watching a group of five Swifts Apus apus above Narborough Park, near Leicester, I saw one suddenly and persistently attack a passing Starling Sturnus vulgaris. The attacks came from behind and below, often making contact with the Starling's belly and vent. The vigour, speed and timing of the 15 or 16 approach pursuits were remarkable and often appeared to treble the flight speed of the Starling, which, even though it jinked and circled, could not evade its pursuer. The attacks ceased when the Starling took refuge in a nearby tree. DAVID NOAKES 41 Trinity Road, St Johns, Narborough, Leicester No member of the Behaviour Notes Panel has ever seen a comparable incident. EDS 378 Notes Observations at Lesser Spotted Woodpecker's nest Between 17.26 and 20.26GMTon 16thJune 1979, nearByfield, Northamptonshire, we watched a nest of Lesser Spotted Woodpeckers Dendrocopos minor. We recorded the number and duration of visits, and removal of faecal material, by the adults; the number of times each adult put its head into the nest-hole on each visit was also recorded, since this might indicate the amount of food brought to the nest. The male visited more frequently (31 out of 46 visits), and put his head in the hole more often on each visit (male mean 7.2, female mean 5.0; Mann-Whitney U-test, P< 0.05), but the length of feeding visits did not differ significantly between sexes (male mean 5.2 seconds, female mean 5.0; P< 0.05). When we ended our watch, the male had remained in the nest for 20 minutes (previous longest period, 34 seconds), so we wonder if the male's habit of incubating at night before the eggs hatch (Bannerman 1955) is continued after hatching. Of 20 faecal pellets removed, the male disposed of 18,12 of these in a concentrated bout before entering the nest for the final time. This nest-sanitation behaviour resembles that of the Great Spotted Woodpecker D. major, largely by the male (Steinfatt 1937), at the end of the day (Blair & Tucker 1941). Faeces were not dropped directly from the hole as reported by Blair & Tucker (1941), but were carried to nearby trees and either dropped or wiped off there. This, too, is as reported for Great Spotted Woodpeckers (Owen 1925), but contrasts with the behaviour of the Green Woodpecker Picus viridis, where a parent (usually the female) swallows the faeces (Owen 1922). The observed predominance of the male Lesser Spotted in nest-sanitation recalls Carlson & Carlson's (1978) record of a male of that species removing a dead nestling from a nest. M. I. AVERY and R. A. COCKERILL Edward Grey Institute of Field Ornithology, South Parks Road, Oxford 0X13PS; Sub-department of Animal Behaviour, Madingley, Cambridge REFERENCES BANNERMAN, D. A. 1955. Birds oj the British Isles, vol. 4. Edinburgh. BLAIR, R. H., & TUCKER, B. W. 1941. Nest sanitation. Brit. Birds 34: 250-255. CARLSON, K., & CARLSON, C. 1978. Lesser Spotted Woodpeckers apparently dismembering dead nestling to remove ft from nest. Brit. Birds 71: 360. OWEN, J. H. 1922. On some breeding habits of woodpeckers. Brit. Birds 15: 61-62. 1925. Notes on the nesting of the Great Spotted Woodpecker. Brit. Birds 19: 125-128. STEINFATT, O. 1937. Beitr. FortPflBiol. Vogel 13: 101-112. Abnormal Sand Martin in Essex At about 07.00 GMT on 30th June 1979, at the Naze Public Open Space, Walton-on-the-Naze, Essex, I watched about a dozen Sand Martins Riparia riparia skimming low over the reserve scrape ponds, a few hundred metres from a breeding colony. One martin seemed to possess two tails: one was quite normal for the species, but the other appeared to grow out from the undertail-coverts, as long again as the normal tail and made up of wispy translucent feathers in a graduated form. The feather shafts could be clearly seen as they flopped about in flight, although they did not inhibit it in any way. A young birdwatcher confirmed what I had seen, and we both watched the bird for about 15 minutes down to about 20m. Eight days later, John Fitzpatrick saw this, or a similar bird, Notes 379 at William Girling Reservoir, approximately 112 km southwest of Walton- on-the-Naze (see below). JOHN K. WESTON 78 Woodberry Way, Walton-on-the-Naze, Essex C0148EW On 8th July 1979, while watching a flock of Sand Martins near William Girling Reservoir, Chingford, Essex, I noticed one with an abnormal growth of white feathering extending from its underparts in a streamer to approximately 30mm beyond the end of its tail. When observed from below at close range, care was taken to note that the white feathering was not a foreign object attached to the belly: no sign of a break or join to indicate the presence of some sticky substance could be seen. I watched the martin for half an hour, during which time it entered a nesting hole containing two young. It was not seen again on two subsequent visits. J. FITZPATRICK 18 Edwick Court, High Street, Cheshunt, Hertfordshire In our opinion, caution should be exercised: we consider that it would be almost impossible to be absolutely certain of the nature of the extra feathering without examination in the hand. EDS Swallows feeding on rising ants In extremely hot weather on 29th August 1979, on the River Ribble at Brungerley Bridge, near Clitheroe, Lancashire, I observed a group of Swallows Hirundo rustica behaving in a manner new to me. Ants Lasius alienus were emerging from their nests and soaring upwards on their nuptial flights, where a host of birds including Black-headed Gulls Laws ridibundus, Sand Martins Riparia riparia, Swallows and House Martins Delichon urbica waited for them. About 10m from where I was lying, five Swallows seemed to be squatting on the ground close to where the ants were emerging and taking the insects before they became airborne; they made no movements that could be interpreted as 'anting'. A further three Swallows were perched in a willow tree Salix full of rising ants. RON FREETHY 15 Lower Manor Lane, Burnley, Lancashire BB12 OEB House Martin feeding young Sand Martins On 6th September 1979, while counting young Sand Martins Riparia riparia at the nesting holes at Filey Brigg, North Yorkshire, I saw a House Martin Delichon urbica land at the entrance to one of the holes where two young Sand Martins were sitting.
Recommended publications
  • 345 Fieldfare Put Your Logo Here
    Javier Blasco-Zumeta & Gerd-Michael Heinze Sponsor is needed. Write your name here Put your logo here 345 Fieldfare Fieldfare. Adult. Male (09-I). Song Thrush FIELDFARE (Turdus pilaris ) IDENTIFICATION 25-26 cm. Grey head; red-brown back; grey rump and dark tail; pale underparts; pale flanks spotted black; white underwing coverts; yellow bill with ochre tip. Redwing Fieldfare. Pattern of head, underwing co- verts and flank. SIMILAR SPECIES Song Thrush has orange underwing coverts; Redwing has reddish underwing coverts; Mistle Thrush has white underwing coverts, but lacks pale supercilium and its rump isn’t grey. Mistle Thrush http://blascozumeta.com Write your website here Page 1 Javier Blasco-Zumeta & Gerd-Michael Heinze Sponsor is needed. Write your name here Put your logo here 345 Fieldfare SEXING Male with dark or black tail feathers; red- dish feathers on back with blackish center; most have a broad mark on crown feathers. Female with dark brown tail feathers but not black; dull reddish feathers on back with dark centre (but not blackish); most have a thin mark on crown feathers. CAUTION: some birds of both sexes have similar pattern on crown feathers. Fieldfare. Sexing. Pattern of tail: left male; right fe- male. Fieldfare. Sexing. Pat- AGEING tern of Since this species doesn’t breed in Aragon, only crown feat- 2 age groups can be recognized: hers: top 1st year autumn/2nd year spring with moult male; bot- limit within moulted chestnut inner greater co- tom female. verts and retained juvenile outer greater coverts, shorter and duller with traces of white tips; pointed tail feathers.
    [Show full text]
  • The Habitat Preference of the Endemic Pygmy Nightjar Nyctipolus Hirundinaceus (Caprimulgidae) of Brazil
    Revista Brasileira de Ornitologia, 22(2), 210-214 ARTICLE June 2014 The habitat preference of the endemic Pygmy Nightjar Nyctipolus hirundinaceus (Caprimulgidae) of Brazil Johan Ingels1,5, Juan Mazar Barnett2, Marcelo Ferreira de Vasconcelos3 and Hilery Desmond Jackson4 1 Galgenberglaan 9, BE-9070 Destelbergen, Belgium. 2 Deceased. 3 Pontifícia Universidade Católica de Minas Gerais, Museu de Ciências Naturais, Avenida Dom José Gaspar, 290, Prédio 41, Coração Eucarístico, CEP 30535-610, Belo Horizonte, Minas Gerais, Brazil. 4 2-6 Beer Court, Kearneys Spring, Toowoomba, QLD 4350, Australia. 5 Corresponding author: [email protected] Received on 10 August 2013. Accepted on 25 December 2013. ABSTRACT: We discuss the choice of habitats for roosting and breeding by the Pygmy Nightjar (Nyctipolus hirundinaceus), a Brazilian endemic from the eastern part of the country. We observed that the choice of nesting and roosting sites of this nightjar is closely connected to open gravelly and stony areas (lajeiros) in the Caatinga and to rocky outcrops (pedras) in the Atlantic Forest, which allows us to conclude that the Pygmy Nightjar is a rupicolous nightjar, preferring rocky substrates for roosting and breeding. KEYWORDS: Caprimulgidae, habitat choice, nesting sites, rocky substrate, roosting sites. INTRODUCTION Cleere 1999). The upperparts of the nominate form hirundinaceus are described as light grayish brown, The Pygmy Nightjar (Nyctipolus hirundinaceus) is one while cearae has a somewhat paler and vielliardi a darker of the smallest Neotropical nightjars (16-20 cm, Cleere plumage (Ribon 1995, Cleere 1998, Holyoak 2001). 1998; 16.5-19 cm, Holyoak 2001), endemic to eastern These differences in general plumage color of the three Brazil, where it is found east of approximately 46°W subspecies are well illustrated by photos in Cleere (2010, (Cleere 1998, Holyoak 2001).
    [Show full text]
  • Foraging Methods of the Song Thrush.-A Recent Review by Clark (Wilson Bull
    September 1976 . GENERAL NOTES 497 the weight loss is impressive, particularly since these caged birds had access to a super- abundant food supply. Ricklefs (1968) analyzed the relationship between maximum nestling weight and average adult weight for individual species. For this he constructed a ratio (R) of the asymptote from the growth curve to the average adult weight. Ratios greater than 1.10 were most common in aerial feeders, while ratios less than 0.90 were most common for ground feeders. Also, species with high R values tended to have long nestling periods. The ratio for Monk Parakeets was 1.28. This was somewhat higher than the intermediate levels that might be expected of an arboreal and ground feeder such as this species. However, the high R value of Monk Parakeets is in accord with what would be expected in species with similarly long nestling periods. Since the energy requirements for nestlings is the sum of maintenance energy and energy for growth, a low growth rate would tend to decrease the rate of energy demand for a nestling. If the number of surviving offspring is limited by the rate at which the parents can deliver energy to the young, then changes in the factors tending to lower the rate of energy demand of the nestlings could increase the number of potential offspring reared by the parents. One way to effect such a change is to lower the growth rate. However a low growth rate also increases the chances for predation and other nest losses by increasing the time in the nest.
    [Show full text]
  • 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.
    [Show full text]
  • Turdus Philomelos)
    The role of blunt egg pole characteristics for recognition of eggs in the song thrush (Turdus philomelos) Lenka Polacikovᡠ1,2,4), Bård G. Stokke3), Petr Procházka2), Marcel Honza2), Arne Moksnes3) & Eivin Røskaft3) (1 Department of Zoology, Palacký University, tr.ˇ Svobody, 26, CZ-771 46 Olomouc, Czech Republic; 2 Institute of Vertebrate Biology, v. v. i., Academy of Sciences of the Czech Republic, Kvetnᡠ8, CZ-603 65 Brno, Czech Republic; 3 Department of Biology, Norwegian University of Science and Technology, NTNU, NO-7491 Trondheim, Norway) (Accepted: 9 November 2009) Summary Colour and speckling of avian eggshells play important roles in egg recognition behaviour. However, only a few studies have paid attention to whether specific parts of eggs may be more important than others in rejection decisions by hosts. We hypothesised that the blunt pole in song thrush (Turdus philomelos) eggs possesses important cues for recognition of own eggs because this is the most visible part of the egg in the nest. We examined host response towards conspecific eggs painted blue either at the blunt or sharp poles, and used unpainted conspecific eggs as a control. We found, as predicted, that the experimental eggs painted blue at the blunt poles were rejected significantly more often than the experimental eggs unpainted at this pole. Rejection rates of experimental eggs were higher with increasing differences in number of spots between the two poles of own eggs. Our results confirmed that the essential cues used for egg discrimination in song thrushes are found at the blunt egg pole. Keywords: brood parasitism, egg discrimination, eggshell characteristics, recognition cues, rejection behaviour.
    [Show full text]
  • Developing Methods for the Field Survey and Monitoring of Breeding Short-Eared Owls (Asio Flammeus) in the UK: Final Report from Pilot Fieldwork in 2006 and 2007
    BTO Research Report No. 496 Developing methods for the field survey and monitoring of breeding Short-eared owls (Asio flammeus) in the UK: Final report from pilot fieldwork in 2006 and 2007 A report to Scottish Natural Heritage Ref: 14652 Authors John Calladine, Graeme Garner and Chris Wernham February 2008 BTO Scotland School of Biological and Environmental Sciences, University of Stirling, Stirling, FK9 4LA Registered Charity No. SC039193 ii CONTENTS LIST OF TABLES................................................................................................................... iii LIST OF FIGURES ...................................................................................................................v LIST OF FIGURES ...................................................................................................................v LIST OF APPENDICES...........................................................................................................vi SUMMARY.............................................................................................................................vii EXECUTIVE SUMMARY ................................................................................................... viii CRYNODEB............................................................................................................................xii ACKNOWLEDGEMENTS....................................................................................................xvi 1. BACKGROUND AND AIMS...........................................................................................2
    [Show full text]
  • 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.
    [Show full text]
  • Nesting of the Acrocephalus Warblers
    Acta zoologica cracoviensia, 46(2): 97-195, Kraków, 30 June, 2003 Nesting of the Acrocephalus warblers Zygmunt BOCHEÑSKI and Piotr KUŒNIERCZYK Received: 14 Feb 2003 Accepted: 26 May 2003 BOCHEÑSKI Z., KUŒNIERCZYK P. 2003. Nesting of the Acrocephalus warblers. Acta zoo- logica cracoviensia, 46(2): 97-195. Abstract. The paper contains data concerning nest sites, material, construction, shape, and sizes in the majority of Acrocephalus species. The descriptions are based on field studies, museum specimens, and literature. The system proposed by CLEMENTS (2000) including 36 species in the genus Acrocephalus has been adopted. Similarities and differ- ences in nesting of 32 species and four subspecies are studied in the last chapter on the ba- sis of 38 characters assembled in Table XLI. They do not always reflect systematic relations of warblers within the genus Acrocephalus on the basis of molecular data. Key words: genus Acrocephalus, nest site, nest material, nest construction, nest shape, nest sizes. Z. BOCHEÑSKI (corresponding author), Institute of Systematics and Evolution of Ani- mals, P.Ac.Sc., 31-016 Kraków, S³awkowska 17, Poland. E-mail: [email protected] P. KUŒNIERCZYK, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, P. Ac.Sc., 53-114 Wroc³aw, Rudolfa Weigla 12, Poland. I. INTRODUCTION The genus Acrocephalus seems not to be defined unequivocally. From time to time it resembles a “witch’s sack”, to which various ornithologists place, according to their predilections, various species of Sylviinae, apart of a few, which are always in this genus. Those additional species are in- cluded in other genera, set up especially for them by other researchers .
    [Show full text]
  • 45) Morocco and Western Sahara – April 2019
    MOROCCO AND WESTERN SAHARA Date - April 2019 Duration - 22 Days Destinations Casablanca - El Jadida - Agadir - Souss-Massa National Park - Arrouais Reserve - Rokein Reserve - Tafraoute - Tizi n’ Test - Ouirgane - Imlil - Toubkal National Park - Ouzoud Falls - Ifrane National Park - Tazekka National Park - Dakhla - Aousserd Trip Overview - Morocco Having come to rely somewhat on his superb spotlighting skills, I decided that it made sense to schedule my return to Morocco for the Easter holiday period, when James would be home from university and available to travel with me once again. Although I appreciate his excellent company even more than his invaluable assistance on what can be fairly demanding tours, neither are luxuries that I will be able to rely upon for a great deal longer, as his studies will require far more of his time during his second year and of course there are now also more personal demands on any remaining free time. We will be travelling to the Congo, both the Republic and Democratic Republic, together in July 2019 to research a great apes tour that I have been planning for some time, but this will probably be our last major trip together for the foreseeable future. If it is, western gorillas and bonobos will be an appropriately spectacular way to conclude what, from my perspective at least, has been an incredibly rewarding experience and I have to say that I am glad that our remarkable journey did not come to an end in Morocco. That is not to suggest that Morocco is not a beautiful country and that our tour was unsuccessful, as neither are the case and we both thoroughly enjoyed exploring what is undoubtedly an alluring and historic destination.
    [Show full text]
  • The Value of Monitoring Wildlife Roadkill
    European Journal of Wildlife Research (2020) 66:18 https://doi.org/10.1007/s10344-019-1357-4 REVIEW The value of monitoring wildlife roadkill Amy L. W. Schwartz1 & Fraser M. Shilling2 & Sarah E. Perkins1 Received: 22 November 2018 /Revised: 20 December 2019 /Accepted: 30 December 2019 # The Author(s) 2020 Abstract The number of wildlife-vehicle collisions has an obvious value in estimating the direct effects of roads on wildlife, i.e. mortality due to vehicle collisions. Given the nature of the data—species identification and location—there is, however, much wider ecological knowledge that can be gained by monitoring wildlife roadkill. Here, we review the added value and opportunities provided by these data, through a series of case studies where such data have been instrumental in contributing to the advance- ment of knowledge in species distributions, population dynamics, and animal behaviour, as well as informing us about health of the species and of the environment. We propose that consistently, systematically, and extensively monitoring roadkill facilitates five critical areas of ecological study: (1) monitoring of roadkill numbers, (2) monitoring of population trends, (3) mapping of native and invasive species distributions, (4) animal behaviour, and (5) monitoring of contaminants and disease. The collection of such data also offers a valuable opportunity for members of the public to be directly involved in scientific data collection and research (citizen science). Through continuing to monitor wildlife roadkill, we can expand our knowledge across a wide range of ecological research areas, as well as facilitating investigations that aim to reduce both the direct and indirect effects of roads on wildlife populations.
    [Show full text]
  • Environmental Assessment and Management
    Public Disclosure Authorized Public Disclosure Authorized Public Disclosure Authorized Banda Field Development - Gas Project Environmental Impact Assessment August 2013 www.erm.com Public Disclosure Authorized FINAL REPORT Tullow Petroleum (Mauritania) Pty Ltd Banda Field development - Gas Project Environmental Impact Assessment August 2013 Prepared by Environmental Resources Management For and on behalf of Environmental Resources Management Approved by: Camille Maclet Signed: Position: Partner Date: 14 August 2013 This report has been prepared by ERM, the trading name of Environmental Resources Management France SAS, with all reasonable skill, care and diligence within the terms of the Contract with the client, incorporating our General Terms and Conditions of Business and taking account of the resources devoted to it by agreement with the client. We disclaim any responsibility to the client and others in respect of any matters outside the scope of the above. This report is confidential to the client and we accept no responsibility of whatsoever nature to third parties to whom this report, or any part thereof, is made known. Any such party relies on the report at their own risk. TABLE OF CONTENTS 1 INTRODUCTION 1 1.1 BACKGROUND 1 1.2 PURPOSE OF THIS REPORT 3 1.3 SCOPE OF THIS EIA 3 1.4 PRESENTATION OF THE PROJECT PROPONENT 3 1.5 PRESENTATION OF THE EIA CONSULTANTS 4 1.6 PURPOSE OF THE EIA 5 1.7 SUMMARY OF THE EIA PROCESS 6 1.8 STRUCTURE OF THIS REPORT 11 2 ADMINISTRATIVE AND REGULATORY FRAMEWORK 13 2.1 INTRODUCTION 13 2.2 NATIONAL ADMINISTRATION
    [Show full text]
  • Bird Species I Have Seen World List
    bird species I have seen U.K tally: 279 US tally: 393 Total world: 1,496 world list 1. Abyssinian ground hornbill 2. Abyssinian longclaw 3. Abyssinian white-eye 4. Acorn woodpecker 5. African black-headed oriole 6. African drongo 7. African fish-eagle 8. African harrier-hawk 9. African hawk-eagle 10. African mourning dove 11. African palm swift 12. African paradise flycatcher 13. African paradise monarch 14. African pied wagtail 15. African rook 16. African white-backed vulture 17. Agami heron 18. Alexandrine parakeet 19. Amazon kingfisher 20. American avocet 21. American bittern 22. American black duck 23. American cliff swallow 24. American coot 25. American crow 26. American dipper 27. American flamingo 28. American golden plover 29. American goldfinch 30. American kestrel 31. American mag 32. American oystercatcher 33. American pipit 34. American pygmy kingfisher 35. American redstart 36. American robin 37. American swallow-tailed kite 38. American tree sparrow 39. American white pelican 40. American wigeon 41. Ancient murrelet 42. Andean avocet 43. Andean condor 44. Andean flamingo 45. Andean gull 46. Andean negrito 47. Andean swift 48. Anhinga 49. Antillean crested hummingbird 50. Antillean euphonia 51. Antillean mango 52. Antillean nighthawk 53. Antillean palm-swift 54. Aplomado falcon 55. Arabian bustard 56. Arcadian flycatcher 57. Arctic redpoll 58. Arctic skua 59. Arctic tern 60. Armenian gull 61. Arrow-headed warbler 62. Ash-throated flycatcher 63. Ashy-headed goose 64. Ashy-headed laughing thrush (endemic) 65. Asian black bulbul 66. Asian openbill 67. Asian palm-swift 68. Asian paradise flycatcher 69. Asian woolly-necked stork 70.
    [Show full text]