Booted Eagle Hieraaetus Pennatus (J
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
A Multi-Gene Phylogeny of Aquiline Eagles (Aves: Accipitriformes) Reveals Extensive Paraphyly at the Genus Level
Available online at www.sciencedirect.com MOLECULAR SCIENCE•NCE /W\/Q^DIRI DIRECT® PHYLOGENETICS AND EVOLUTION ELSEVIER Molecular Phylogenetics and Evolution 35 (2005) 147-164 www.elsevier.com/locate/ympev A multi-gene phylogeny of aquiline eagles (Aves: Accipitriformes) reveals extensive paraphyly at the genus level Andreas J. Helbig'^*, Annett Kocum'^, Ingrid Seibold^, Michael J. Braun^ '^ Institute of Zoology, University of Greifswald, Vogelwarte Hiddensee, D-18565 Kloster, Germany Department of Zoology, National Museum of Natural History, Smithsonian Institution, 4210 Silver Hill Rd., Suitland, MD 20746, USA Received 19 March 2004; revised 21 September 2004 Available online 24 December 2004 Abstract The phylogeny of the tribe Aquilini (eagles with fully feathered tarsi) was investigated using 4.2 kb of DNA sequence of one mito- chondrial (cyt b) and three nuclear loci (RAG-1 coding region, LDH intron 3, and adenylate-kinase intron 5). Phylogenetic signal was highly congruent and complementary between mtDNA and nuclear genes. In addition to single-nucleotide variation, shared deletions in nuclear introns supported one basal and two peripheral clades within the Aquilini. Monophyly of the Aquilini relative to other birds of prey was confirmed. However, all polytypic genera within the tribe, Spizaetus, Aquila, Hieraaetus, turned out to be non-monophyletic. Old World Spizaetus and Stephanoaetus together appear to be the sister group of the rest of the Aquilini. Spiza- stur melanoleucus and Oroaetus isidori axe nested among the New World Spizaetus species and should be merged with that genus. The Old World 'Spizaetus' species should be assigned to the genus Nisaetus (Hodgson, 1836). The sister species of the two spotted eagles (Aquila clanga and Aquila pomarina) is the African Long-crested Eagle (Lophaetus occipitalis). -
Studies of Less Familiar Birds Ij2 Lesser Spotted Eagle B.-U
Studies of less familiar birds ij2 Lesser Spotted Eagle B.-U. Meyburg Plates 61-64. Of all European eagles, the Lesser Spotted Eagle Aquila pomarina has the smallest world breeding range, the nominate race being confined to eastern parts of Germany, Poland, eastern Czechoslovakia, Hun gary, Yugoslavia, Romania, Bulgaria, north-east Greece, western Turkey (Thrace), and the Soviet Union north to Leningrad and east to about 35°E. There are no published records of proved breeding in eastern Austria this century, though pairs from Hungary hunt over the land around Lake Neusiedl. There is no clear information on the current position in the Caucasus and the south Caspian lowlands. In Germany the breeding area stretches only to the north of Berlin, westwards beyond the rivers Oder and Neisse but stopping short of the Elbe. In 1969 there were 53 known broods in this area, and possibly a further nine (H. Weber in Glutz von Blotzheim et al. 1971). Even at the beginning of this century, the breeding range extended much further westwards, at least as far as the River Weser in Niedersachsen. A second subspecies, A. p. hastata, breeds in parts of India, in particular the Ganges Valley and West Bengal, and also in Bangla Desh. Hardly anything is known about this form, which appears to be rare. The first autumn plumage is said to be quite different from that of the nominate race, which has led some authors to treat it as a separate species. The Lesser Spotted Eagle presents a very difficult problem to field and museum ornithologists alike—the clear differentiation between it and the very closely related Spotted Eagle A. -
Iucn Red Data List Information on Species Listed On, and Covered by Cms Appendices
UNEP/CMS/ScC-SC4/Doc.8/Rev.1/Annex 1 ANNEX 1 IUCN RED DATA LIST INFORMATION ON SPECIES LISTED ON, AND COVERED BY CMS APPENDICES Content General Information ................................................................................................................................................................................................................................ 2 Species in Appendix I ............................................................................................................................................................................................................................... 3 Mammalia ............................................................................................................................................................................................................................................ 4 Aves ...................................................................................................................................................................................................................................................... 7 Reptilia ............................................................................................................................................................................................................................................... 12 Pisces ................................................................................................................................................................................................................................................. -
Nuweveld North Wind Farm
Nuweveld North Wind Farm Red Cap Nuweveld North (Pty) Ltd Avifaunal assessment October 2020 REPORT REVIEW & TRACKING Document title Nuweveld North Wind Farm - Avifaunal Impact study (Scoping Phase) Client name Patrick Killick Aurecon Status Final-for client Issue date October 2020 Lead author Jon Smallie – SACNASP 400020/06 WildSkies Ecological Services (Pty) Ltd 36 Utrecht Avenue, East London, 5241 Jon Smallie E: [email protected] C: 082 444 8919 F: 086 615 5654 2 Regulation GNR 326 of 4 December 2014, as amended 7 April 2017, Appendix 6 Section of Report (a) details of the specialist who prepared the report; and the expertise of that specialist to Appendix 5 compile a specialist report including a curriculum vitae ; (b) a declaration that the specialist is independent in a form as may be specified by the Appendix 6 competent authority; (c) an indication of the scope of, and the purpose for which, the report was prepared; Section 1.1 & 2 .1 an indication of the quality and age of base data used for the specialist report; Section 3 a description of existing impacts on the site, cumulative impacts of the proposed development Section 3.8 and levels of acceptable change; (d) the duration, date and season of the site investigation and the relevance of the season to Section 2.5 to 2.7 the outcome of the assessment; (e) a description of the methodology adopted in preparing the report or carrying out the Section 2 specialised process inclusive of equipment and modelling used; (f) details of an assessment of the specific identified sensitivity -
Studies of Less Familiar Birds 161 Booted Eagle R
Studies of less familiar birds 161 Booted Eagle R. F. Porter Photographs by Pierre Petit, M. D. England and A. N. H. Peach Plates j 2- j 8 The Booted Eagle Hkramtus pennatus is a small eagle similar in size to a Buzzard Buteo buteo, but of slimmer build, with narrower wings and a longer tail. In flight its proportions are not unlike those of a Black Kite Mikus migrans, though the tail is square-ended, not forked (plate 58). When perched, its long feathered tarsi, or 'boots', are characteristic (plate 53b). The species is dimorphic, a feature which, among European birds of prey, it shares only with Eleonora's Falcon Fa/co eleonorae. Many raptors show considerable plumage variations, but in most cases these take the form of clines from very pale to very dark through a whole range of intermediates. The Booted Eagle has two very distinct phases—a light and a dark. This dimorphism is exhibited by both sexes; breeding pairs frequently consist of one dark and one light and their offspring may be either light or dark. Both phases are brilliantly illustrated in plates 52-58. The light phase has a lightly streaked tawny-rufous head and neck, with a white forehead and superciliary stripe and dark tawny-brown ear-coverts and cheeks. The under-parts are white with rufous streaks on the chin, upper breast and flanks (plates 5 5 a and b), and the under wing-coverts are also white with brownish flecks (plate 5 8b). Im- matures look more 'gingery' below. The white under-parts extend on to the 'shoulder' to form a white patch (especially plate 5 2). -
Repeated Sequence Homogenization Between the Control and Pseudo
Repeated Sequence Homogenization Between the Control and Pseudo-Control Regions in the Mitochondrial Genomes of the Subfamily Aquilinae LUIS CADAH´IA1*, WILHELM PINSKER1, JUAN JOSE´ NEGRO2, 3 4 1 MIHAELA PAVLICEV , VICENTE URIOS , AND ELISABETH HARING 1Molecular Systematics, 1st Zoological Department, Museum of Natural History Vienna, Vienna, Austria 2Department of Evolutionary Ecology, Estacio´n Biolo´gica de Don˜ana, Sevilla, Spain 3Centre of Ecological and Evolutionary Synthesis (CEES), Department of Biology, Faculty for Natural Sciences and Math, University of Oslo, Oslo, Norway 4Estacio´n Biolo´gica Terra Natura (Fundacio´n Terra Natura—CIBIO), Universidad de Alicante, Alicante, Spain ABSTRACT In birds, the noncoding control region (CR) and its flanking genes are the only parts of the mitochondrial (mt) genome that have been modified by intragenomic rearrangements. In raptors, two noncoding regions are present: the CR has shifted to a new position with respect to the ‘‘ancestral avian gene order,’’ whereas the pseudo-control region (CCR) is located at the original genomic position of the CR. As possible mechanisms for this rearrangement, duplication and transposition have been considered. During characterization of the mt gene order in Bonelli’s eagle Hieraaetus fasciatus, we detected intragenomic sequence similarity between the two regions supporting the duplication hypothesis. We performed intra- and intergenomic sequence comparisons in H. fasciatus and other falconiform species to trace the evolution of the noncoding mtDNA regions in Falconiformes. We identified sections displaying different levels of similarity between the CR and CCR. On the basis of phylogenetic analyses, we outline an evolutionary scenario of the underlying mutation events involving duplication and homogenization processes followed by sporadic deletions. -
The Eagle Genus Hieraaetus Is Distinct from Aquila, with Comments on the Name Ayres’ Eagle
William S. Clark 295 Bull. B.O.C. 2012 132(4) The eagle genus Hieraaetus is distinct from Aquila, with comments on the name Ayres’ Eagle by William S. Clark Received 16 April 2012 Consensus has long existed among taxonomists as to the placement of the species of the eagles in the genera Aquila and Hieraaetus, the only exception being Wahlberg’s Eagle, which has been treated either as A. wahlbergi or H. wahlbergi. However, recent comparisons of DNA sequences of these eagles revealed that both genera were polyphyletic (Helbig et al. 2005, Lerner & Mindell 2005, Griffiths et al. 2007, Haring et al. 2007). To ensure monophyly, these authors recommended that some species be moved into and out of both genera and placed Wahlberg’s Eagle definitely in Hieraaetus. On the other hand, Sangster et al. (2005) recommended that Hieraaetus be subsumed into Aquila, for which they cite eight recent phylogenetic studies, only four of them published in peer-reviewed journals (Roulin & Wink 2004, Bunce et al. 2005, Helbig et al. 2005, Lerner & Mindell 2005); all of which, nevertheless, retained Hieraaetus. Thus, none of the four peer-reviewed journal articles cited by Sangster et al. (2005) to justify placing Hieraaetus into Aquila actually recommended this. Further, Sangster et al. (2005) proposed only that Booted Eagle (pennatus) be included in Aquila, because their recommendations only considered European birds. The generic treatment of Sangster et al. (2005) was followed without comment by Gjershaug et al. (2009) in describing Weiske’s or Pygmy Eagle (weiskei) as a species separate from Little Eagle H. -
Habitat Preferences of Bonelli's Eagles Aquila Fasciata in Sicily
Bird Study (2012) 59, 207–217 Habitat preferences of Bonelli’s Eagles Aquila fasciata in Sicily MASSIMILIANO DI VITTORIO1, MAURIZIO SARA` 1 and PASCUAL LO´ PEZ-LO´ PEZ2∗ 1Department of Environmental Biology and Biodiversity, University of Palermo, Via Archirafi 18, 93100 Palermo, Italy and 2Vertebrate Zoology Research Group, Instituto Universitario de Investigacio´n CIBIO, University of Alicante, Campus San Vicente del Raspeig, Edificio Ciencias III, 03080 Alicante, Spain Capsule For breeding, areas dominated by extensive agricultural and rugged Mediterranean landscapes are preferred; maintenance of habitat heterogeneity and extensive agriculture are key for the conservation of this eagle. Aims To model breeding habitat preferences of Bonelli’s Eagles Aquila fasciata in Sicily, where the last viable population still remains in Italy, in order to identify the most important habitats for conservation. Methods Pairs were monitored between 1990 and 2010. A case-control design through GLMs was used at two spatial scales: landscape and home-range. Variables included topographic, climatic, land-use, road and descriptors of habitat heterogeneity. Information-based criteria were used to select the best subset of predictors. Results A total of 22 breeding pairs are still breeding, which represent about the 90% of the Italian popu- lation. The best models at both scales showed that Bonelli’s Eagles were clearly associated with Mediterra- nean features, including rugged areas surrounded by extensive arable land, shrubland and herbaceous vegetation. Our results emphasize the negative effects of habitat fragmentation and agricultural intensifica- tion on the probability of occurrence of Bonelli’s Eagles. Conclusion The distribution of Bonelli’s Eagles in Sicily can be described by a relatively small number of topographical and land-use variables. -
Cooperative Nesting by a Trio of Booted Eagles &Lpar;<I>Hieraaetus
92 SHORT COMMUNICATIONS VOL. 39, NO. 1 y los polluelos salieron de los nidos entre noviembrey DELHOYO, J., A. ELLIOTT,AND J. SARGATAL(EDS.). 1994 diciembre. Los nidos fueron de construcci6nendeble y Handbook of the birds of the world. Vol. 2. New constituidospor ramas secasy se situaron en las bifur- World Vultures to Guineafowl. Lynx Edicions, Barce- cacionesde las ramas de firboles a una altura promedio lona, Spain. de 15 m sobre el suelo (N = 3). Las dimensionespro- FERGUSON-LEE,J. AND D.A. CHRISTIE.2001. Raptors of the medio de los nidos fueron 39.5 X 39.5 cm y 13.9 cm de world. Houghton Mifflin Company, Boston, MA profundidadexterior, con una copa de 21.5 x 22.5 cm y U.S.A. 7 8 cm de profundidad.E1 tamafio modal de la nidada FERRARI,S.F. 1990. A foraging associationbetween two fue dos (N = 3 nidos). Los huevospresentaron manchas kite species(Ictinia plumbeaand Leptodoncayanensis) de color car6 con marcas mils ruerres en la base (N = 6 and buffy-headed marmosets (Callithrixfiaviceps) in huevos)y tuvieronun tamafio promedio de 51.5 x 40.8 southeastern Brazil. Condor 92:781-783. mm (N = 4). Los polluelos eclosionaronde forma asin- FOSTER,n.s. 1971. Plumage and behavior of a juvenile cr6nica. En total, de tres intentos de nidificaci6n, dos Gray-headedKite. Auk 88:163-166. polluelos emplumaron exitosamente,lo que representa HAVERSCHMIDT,F. 1962. Notes on the feeding habitsand un 6xito de nidificaci6ndel 66.6%. Todaslas presas11e- food of some hawks in Surinam. Condor 64:154-158. vadasa los polluelosen el nido fueron serpientes(N = LINS, L.V. -
Accipitridae Species Tree
Accipitridae I: Hawks, Kites, Eagles Pearl Kite, Gampsonyx swainsonii ?Scissor-tailed Kite, Chelictinia riocourii Elaninae Black-winged Kite, Elanus caeruleus ?Black-shouldered Kite, Elanus axillaris ?Letter-winged Kite, Elanus scriptus White-tailed Kite, Elanus leucurus African Harrier-Hawk, Polyboroides typus ?Madagascan Harrier-Hawk, Polyboroides radiatus Gypaetinae Palm-nut Vulture, Gypohierax angolensis Egyptian Vulture, Neophron percnopterus Bearded Vulture / Lammergeier, Gypaetus barbatus Madagascan Serpent-Eagle, Eutriorchis astur Hook-billed Kite, Chondrohierax uncinatus Gray-headed Kite, Leptodon cayanensis ?White-collared Kite, Leptodon forbesi Swallow-tailed Kite, Elanoides forficatus European Honey-Buzzard, Pernis apivorus Perninae Philippine Honey-Buzzard, Pernis steerei Oriental Honey-Buzzard / Crested Honey-Buzzard, Pernis ptilorhynchus Barred Honey-Buzzard, Pernis celebensis Black-breasted Buzzard, Hamirostra melanosternon Square-tailed Kite, Lophoictinia isura Long-tailed Honey-Buzzard, Henicopernis longicauda Black Honey-Buzzard, Henicopernis infuscatus ?Black Baza, Aviceda leuphotes ?African Cuckoo-Hawk, Aviceda cuculoides ?Madagascan Cuckoo-Hawk, Aviceda madagascariensis ?Jerdon’s Baza, Aviceda jerdoni Pacific Baza, Aviceda subcristata Red-headed Vulture, Sarcogyps calvus White-headed Vulture, Trigonoceps occipitalis Cinereous Vulture, Aegypius monachus Lappet-faced Vulture, Torgos tracheliotos Gypinae Hooded Vulture, Necrosyrtes monachus White-backed Vulture, Gyps africanus White-rumped Vulture, Gyps bengalensis Himalayan -
Phylogeny, Historical Biogeography and the Evolution of Migration in Accipitrid Birds of Prey (Aves: Accipitriformes)
Ornis Hungarica 2014. 22(1): 15–35. DOI: 10.2478/orhu-2014-0008 Phylogeny, historical biogeography and the evolution of migration in accipitrid birds of prey (Aves: Accipitriformes) Jenő nagy1 & Jácint tökölyi2* Jenő Nagy & Jácint Tökölyi 2014. Phylogeny, historical biogeography and the evolution of mig ration in accipitrid birds of prey (Aves: Accipitriformes). – Ornis Hungarica 22(1): 15–35. Abstract Migration plays a fundamental part in the life of most temperate bird species. The re gu lar, largescale seasonal movements that characterize temperate migration systems appear to have originated in parallel with the postglacial northern expansion of tropical species. Migratoriness is also in- fluenced by a number of ecological factors, such as the ability to survive harsh winters. Hence, understanding the origins and evolution of migration requires integration of the biogeographic history and ecology of birds in a phylogenetic context. We used molecular dating and ancestral state reconstruction to infer the origins and evolu- tionary changes in migratory behavior and ancestral area reconstruction to investigate historical patterns of range evolution in accipitrid birds of prey (Accipitriformes). Migration evolved multiple times in birds of prey, the ear- liest of which occurred in true hawks (Accipitrinae), during the middle Miocene period, according to our analy- ses. In most cases, a tropical ancestral distribution was inferred for the nonmigratory ancestors of migratory line- ages. Results from directional evolutionary tests indicate that migration evolved in the tropics and then increased the rate of colonization of temperate habitats, suggesting that temperate species might be descendants of tropi- cal ones that dispersed into these seasonal habitats. -
Arabian Peninsula
THE CONSERVATION STATUS AND DISTRIBUTION OF THE BREEDING BIRDS OF THE ARABIAN PENINSULA Compiled by Andy Symes, Joe Taylor, David Mallon, Richard Porter, Chenay Simms and Kevin Budd ARABIAN PENINSULA The IUCN Red List of Threatened SpeciesTM - Regional Assessment About IUCN IUCN, International Union for Conservation of Nature, helps the world find pragmatic solutions to our most pressing environment and development challenges. IUCN’s work focuses on valuing and conserving nature, ensuring effective and equitable governance of its use, and deploying nature-based solutions to global challenges in climate, food and development. IUCN supports scientific research, manages field projects all over the world, and brings governments, NGOs, the UN and companies together to develop policy, laws and best practice. IUCN is the world’s oldest and largest global environmental organization, with almost 1,300 government and NGO Members and more than 15,000 volunteer experts in 185 countries. IUCN’s work is supported by almost 1,000 staff in 45 offices and hundreds of partners in public, NGO and private sectors around the world. www.iucn.org About the Species Survival Commission The Species Survival Commission (SSC) is the largest of IUCN’s six volunteer commissions with a global membership of around 7,500 experts. SSC advises IUCN and its members on the wide range of technical and scientific aspects of species conservation, and is dedicated to securing a future for biodiversity. SSC has significant input into the international agreements dealing with biodiversity conservation. About BirdLife International BirdLife International is the world’s largest nature conservation Partnership. BirdLife is widely recognised as the world leader in bird conservation.