A Case of Cooperative Hunting by a Pair of Northern Goshawks
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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. -
The Use of Green Plant Material in Bird Nests to Avoid Ectoparasites
July1984] ShortCommunications 615 the Spot-wingedFalconet may not benefitthe Monk HoY, G. 1980. Notas nidobio16gicasdel noroestear- Parakeet in such a manner. gentino. II. Physis (Buenos Aires), Secc. C, 39 We are grateful to A. G6mez Dur&n and J. C. Vera (96): 63-66. (INTA) for grantingus the useof the fieldwork areas, MACLEAN,G.L. 1973. The SociableWeaver, part 4: to N. Arguello and M. Nores for their assistancein predators, parasites and symbionts. Ostrich 44: the identification of food remains, and to J. Navarro 241-253. for his help in the field. This work wassupported by STRANECK,R., & G. VASINA. 1982. Unusual behav- a grant from the Subsecretariade Ciencia y Tecno- iour of the Spot-winged Falconet (Spiziapteryx logla (SUBCYT) of Argentina. circumcinctus).Raptor Res. 16: 25-26. LITERATURE CITED Received7 July 1983, accepted21 February1984. DEAN, A. 1971. Notes on Spiziapteryxcircumcinctus. Ibis 113: 101-102. The Use of Green Plant Material in Bird Nests to Avoid Ectoparasites PETER H. WIMBERGER 1 ZoologyDivision, Washington State Museum DB-10, Universityof Washington, Seattle,Washington 98105 USA Certain birds characteristicallyplace green plant causesnestling mortality in and nest desertion by material in their nests.This greenery is not part of birds (Webster 1944, Neff 1945, Fitch et al. 1946, Moss the nest structureproper but is placed haphazardly and Camin 1970, Feare 1976,Wheelwright and Boers- around the edges or inside the nest. The birds re- ma 1979).In general,the increasedmortality due to plenishthe spraysof greenmaterial, often daily, dur- ectoparasitesis causedby the loss of blood, which ing incubation and the nestling period (Brown and weakens the host, by viral disease, or by disease Amadon 1968, Beebe1976, pers. -
Estimations Relative to Birds of Prey in Captivity in the United States of America
ESTIMATIONS RELATIVE TO BIRDS OF PREY IN CAPTIVITY IN THE UNITED STATES OF AMERICA by Roger Thacker Department of Animal Laboratories The Ohio State University Columbus, Ohio 43210 Introduction. Counts relating to birds of prey in captivity have been accomplished in some European countries; how- ever, to the knowledge of this author no such information is available in the United States of America. The following paper consistsof data related to this subject collected during 1969-1970 from surveys carried out in many different direc- tions within this country. Methods. In an attempt to obtain as clear a picture as pos- sible, counts were divided into specific areas: Research, Zoo- logical, Falconry, and Pet Holders. It became obvious as the project advanced that in some casesthere was overlap from one area to another; an example of this being a falconer working with a bird both for falconry and research purposes. In some instances such as this, the author has used his own judgment in placing birds in specific categories; in other in- stances received information has been used for this purpose. It has also become clear during this project that a count of "pets" is very difficult to obtain. Lack of interest, non-coop- eration, or no available information from animal sales firms makes the task very difficult, as unfortunately, to obtain a clear dispersal picture it is from such sourcesthat informa- tion must be gleaned. However, data related to the importa- tion of birds' of prey as recorded by the Bureau of Sport Fisheries and Wildlife is included, and it is felt some observa- tions can be made from these figures. -
Common Birds of Namibia and Botswana 1 Josh Engel
Common Birds of Namibia and Botswana 1 Josh Engel Photos: Josh Engel, [[email protected]] Integrative Research Center, Field Museum of Natural History and Tropical Birding Tours [www.tropicalbirding.com] Produced by: Tyana Wachter, R. Foster and J. Philipp, with the support of Connie Keller and the Mellon Foundation. © Science and Education, The Field Museum, Chicago, IL 60605 USA. [[email protected]] [fieldguides.fieldmuseum.org/guides] Rapid Color Guide #584 version 1 01/2015 1 Struthio camelus 2 Pelecanus onocrotalus 3 Phalacocorax capensis 4 Microcarbo coronatus STRUTHIONIDAE PELECANIDAE PHALACROCORACIDAE PHALACROCORACIDAE Ostrich Great white pelican Cape cormorant Crowned cormorant 5 Anhinga rufa 6 Ardea cinerea 7 Ardea goliath 8 Ardea pupurea ANIHINGIDAE ARDEIDAE ARDEIDAE ARDEIDAE African darter Grey heron Goliath heron Purple heron 9 Butorides striata 10 Scopus umbretta 11 Mycteria ibis 12 Leptoptilos crumentiferus ARDEIDAE SCOPIDAE CICONIIDAE CICONIIDAE Striated heron Hamerkop (nest) Yellow-billed stork Marabou stork 13 Bostrychia hagedash 14 Phoenicopterus roseus & P. minor 15 Phoenicopterus minor 16 Aviceda cuculoides THRESKIORNITHIDAE PHOENICOPTERIDAE PHOENICOPTERIDAE ACCIPITRIDAE Hadada ibis Greater and Lesser Flamingos Lesser Flamingo African cuckoo hawk Common Birds of Namibia and Botswana 2 Josh Engel Photos: Josh Engel, [[email protected]] Integrative Research Center, Field Museum of Natural History and Tropical Birding Tours [www.tropicalbirding.com] Produced by: Tyana Wachter, R. Foster and J. Philipp, -
Quantifying the Global Legal Trade in Live CITES-Listed Raptors and Owls
Electronic Supplementary Material (Panter et al. 2019) Electronic Supplementary Material for: Quantifying the global legal trade in live CITES-listed raptors and owls for commercial purposes over a 40-year period Published in 2019 in Avocetta 43(1) :23-36; doi: https://doi.org/10.30456/AVO.2019104 Authors: Connor T. Panter1,*, Eleanor D. Atkinson1, Rachel L. White1 1 School of Pharmacy and Biomolecular Sciences, University of Brighton, Brighton, United Kingdom. * Corresponding author: [email protected] List of contents: ESM 1 - Appendix A. CITES source categories with associated definitions. ESM 2 - Appendix B. CITES Trade Purposes categories with associated definitions. ESM 3 - Appendix C. CITES Importer and Exporter countries with total reported imported and exported individuals of raptors and owls. ESM 4 - Appendix D. Raptor and owl exporter countries supplying the Japanese trade in live birds for commercial use. ESM 5 - Appendix E. Percentages of number of traded species within global IUCN Red List categories and population trends. ESM 6. Imported raptor species, number of imported individuals and percentage of total imported raptor individuals. ESM 7. Exported raptor species, number of exported individuals and percentage of total exported raptor individuals. ESM 8. Imported owl species, number of imported individuals and percentage of total imported owl individuals. ESM 9. Exported owl species, number of exported individuals and percentage of total exported owl individuals. 1 Electronic Supplementary Material (Panter et al. 2019) ELECTRONIC SUPPLEMENTARY MATERIAL (ESM) ESM 1 - Appendix A. CITES source categories with associated definitions. *The CITES Trade Database does not provide information regarding whether birds declared as “wild- caught” were derived from legal or illegal activities. -
PETITION to LIST the QUEEN CHARLOTTE GOSHAWK Accipiter Gentilis Laingi AS a FEDERALLY ENDANGERED SPECIES
PETITION TO LIST THE QUEEN CHARLOTTE GOSHAWK Accipiter gentilis laingi AS A FEDERALLY ENDANGERED SPECIES May 2, 1994 May 2, 1994 Mr. Bruce Babbitt Secretary of the Interior Department of the Interior 18th and "C" Street, N.W. Washington, D.C. 20240 Dear Mr. Babbitt, The Southwest Center for Biological Diversity, the Greater Gila Biodiversity Project, the Biodiversity Legal Foundation, Greater Ecosystem Alliance, Save the West, Save America's Forests, Native Forest Network, Native Forest Council, Peter Galvin, Eric Holle, and Don Muller hereby formally petition to list the Queen Charlotte goshawk (Accipiter gentilis laingi) as endangered pursuant to the Endangered Species Act, 16 U.S.C. 1531 et seg. This petition is filed under 5 U.S.C. 553(e) and 50 C.F.R 424.14(a) which grant interested parties the right to petition for issue of a rule from the Assistant Secretary of the Interior. Petitioners also request that Critical Habitat be designated for the Queen Charlotte goshawk concurrent with the listing, pursuant to 50 C.F.R 424.12, and pursuant to the Administrative Procedures Act 5 U.S.C. 553. Petitioners understand that this petition action sets in motion a specific process placing definite response requirements on the U.S. Fish and Wildlife Service and very specific time constraints upon those responses. Petitioners The Southwest Center for Biological Diversity is dedicated to protecting and restoring the Southwest's island forests and desert rivers by aggressively advocating for every level of biotic diversity, from butterflies to jaguars. This petition is part of the Center's ongoing efforts to conserve goshawks throughout the West. -
Wave Moult of the Primaries in Accipitrid Raptors, and Its Use in Ageing Immatures
Chancellor, R. D. & B.-U. Meyburg eds. 2004 Raptors Worldwide WWGBP/MME Wave Moult of the Primaries in Accipitrid raptors, and its use in ageing immatures William S. Clark ABSTRACT Stresemann & Stresemann (1966) described wave moult in the primary remiges ('Staffelmauser' in German; also translated as 'step-wise moult') for some families of birds but not for Acccipitrid raptors, even though many of the species in this family (especially the larger ones) show it. Primaries of Accipitrid raptors are replaced from Pl (inner) sequentially outward. Waves are formed when not all of the ten primaries are replaced in any annual moult cycle. In the next annual cycle, moult begins anew at Pl as well as continuing with the next feather from where it left off in the last cycle. Two or three, occasionally four, wave fronts of new primaries can be seen in the primaries of some raptors, especially larger ones, e.g., eagles. Knowledge and understanding of wave moult can ascertain the ages of immature raptors in those species that take three or four years to attain adult plumage, as these species typically do not replace all of the primaries in any moult cycle. Juvenile eagles show all primaries the same age. Second plumage eagles show two ages of primaries, newer inner ones and older retained juvenile outer ones. Third plumage eagles show two waves, with the first wave proceeding to P8, P9, or PIO, and the second to P3, P4, P5, or P6. Fourth plumage eagles usually show new outer PlO from the first wave, new P5 to P7 from the second wave, and new Pl to P3 from the most recent wave. -
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. -
Accipitridae, Aves
AMERICAN MUSEUM Norntates PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CENTRAL PARK WEST AT 79TH STREET, NEW YORK, N.Y. 10024 Number 2741, pp. 1-20, figs. 1-4, table 1 July 30, 1982 A Revision of the Sub-Buteonine Hawks (Accipitridae, Aves) DEAN AMADON1 ABSTRACT This paper is a taxonomic review of the 25 species. Changes from usual treatment include rec- species and approximately 10 genera of chiefly ognition ofthe genus Asturina, merger ofthe genus Neotropical hawks called sub-buteonines and al- Heterospizias with Buteogallus, and transfer ofthe lied to the more advanced genus Buteo. Generic genus Geranospiza to the sub-buteonines. Finally, diagnoses supported by logarithmic ratio diagrams the broad systematics of the chief components of of measurements are presented along with com- the family Accipitridae and the place of the sub- ments on intraspecific variation in a few of the buteonine group within it are discussed. INTRODUCTION The term "sub-buteonines" is here used Eight of the 10 sub-buteonine genera here for a group ofhawks and eagles closely allied recognized are Neotropical. Three of the to the large and nearly cosmopolitan genus species in as many genera, cross the United Buteo. As noted later, certain other genera or States border. Two of them, Asturina nitida groups ofgenera may be regarded as sub-bu- and Buteogallus anthracinus, have distribu- teonines in a more general sense, but they are tions that are primarily tropical and subtrop- less closely allied to Buteo and beyond the ical. The third, Parabuteo unicinctus, extends main scope ofthe present paper. As the name a little farther north to Kansas and farther implies and as defined below the sub-bu- south to central Chile. -
Short Communications Short Communications
16 Short communications Short communications Bat-hunting behaviour of the Dark Chanting Goshawk Melierax metabates The Dark Chanting Goshawk Melierax metabates (weighing between 645 and 850 g (Kemp 1994)) is known to prey on reptiles, birds, rodents, amphibians and insects (Kemp 1994, Ferguson-Lees & Christie 2001, Dean & Milton 2005), including termite alates (BPF, pers. obs.). Here we report, for the first time according to our knowledge, on bat-hunting behaviour by this bird species. The observations were made near the Seronera Research Centre, Serengeti National Park (SNP), Tanzania (2º 26’S, 34º 51’E; 1535 m). The Dark Chanting Goshawk is a commonly occurring breeding resident of the open woodlands in the SNP (Zimmerman et al. 2001). At 18:30 (dusk) on 20 September 2007, six African Sheath-tailed Bats Coleura afra which weigh between 10 and 12 g (Dunlop 1997) were observed leaving their day roost located under the roof of the residential house of the research station. (NB: the bats were identified from digital pictures and videos using the Kingdon (1997) mammal guide). A Dark Chanting Goshawk of unknown sex glided down from a branch (c. 5 m high) of a nearby tree (Acacia tortilis), where it had positioned itself prior, and plunged down among the dispersing group of bats. The individual stooped with stretched legs and spread-out talons in between the flying bats. The raptor made a second similar attack after a turning manoeuvre in mid-air before returning to its original perch. Two minutes later a new group of four more sheath-tailed bats left the roost using the same exit and once more the goshawk launched a similar mid- air attack with spread tail feathers. -
Pale Chanting Goshawk
232 Accipitridae: vultures, kites, hawks, eagles, buzzards and harriers Movements: Some birds remain in their territories through- out the year but others are known to show extensive move- ments (Biggs et al. 1984). SAFRING ring recovery data show that females disperse an average distance of 282 km (range 16–731 km), and males 39 km (range 0–132 km). The seasonal patterns should not be interpreted as move- ments to and from Zones, but are probably the result of an increase in the number of observable birds once juveniles reach independence (February–June) and a decrease in ob- servations when birds, especially females, are confined to their nesting sites during the breeding season (August– December). Breeding: The breeding season starts in July–August, peaks October–November and tails off in May. This ‘tail’ may be the result of a post-fledging dependence period of longer than seven weeks (Maclean 1993b). Egglaying in southern Africa spans March–December, with a July–Sep- tember peak (Malan 1995). Breeding during the atlas period was reported throughout its range, most frequently from the northern Cape Province and southern Namibia (Zone 3). This could reflect the greater ease of locating nests in these more open regions. Interspecific relationships: The range of the Pale Chanting Goshawk overlaps marginally with that of the Dark Chanting Goshawk in the far northern Transvaal, northern and eastern Botswana and in southwestern Zim- babwe, but even there it is more common than the Dark Chanting Goshawk (M. Herremans pers. comm.). In areas of overlap, the Pale Chanting Goshawk inhabits more arid and open scrub (Steyn 1982b).