S EAGLE &Lpar;<I>HIERAAETUS FASCIATUS</I>&Rpar

Total Page:16

File Type:pdf, Size:1020Kb

S EAGLE &Lpar;<I>HIERAAETUS FASCIATUS</I>&Rpar j RaptorRes. 33 (2) :110-116 ¸ 1999 The Raptor ResearchFoundation, Inc. SELECTION OF NEST CLIFFS BY BONELLI'S EAGLE (HIETUS FASCIATUS) IN SOUTHEASTERN SPAIN DIEGO ONTIVEROS Departamentode Biologia Animal y Ecolog•a,Facultad de Ciencias,Universidad de Granada,E-18071 Granada, Spain PmSTP•CT.---Atotal of 119 nestsand 52 cliffsoccupied by 32 Bonelli'sEagle (Hieraaetusfasciatus)pairs wasstudied during 1995-97 in southeasternSpain. Mean numberof nestsbuilt by pairsexceeded that reportedin previousstudies (i = 3.7; N = 32) and therewas a trend amongeagles to build their nests with a southeasternorientation. Breeding density was directly related to the availabilityof cliffs.Eagles occupiedhigher cliffs (i = 52.9 m; N = 32), locatedon steeperslopes (i = 34.7ø;N = 31) than was available.Occupied cliffs were highly heterogeneousdue to the fact that use of differentareas by Bonelli's Eagleswas dependent on human disturbance.Thus, occupied cliffs with the shortestlinear distanceto pavedroads were higher than occupiedcliffs far from pavedroads. Selection of high cliffs located on steep slopeswith southern orientationsmay have been associatedwith the additionallift providedeagles, since these types of nest sitesenhanced the possibilityof thermal and slopesoaring. Preservation of nest cliffs free from disturbances should be undertaken to ensure the survival of Bonelli's Eagle in this area of Spain. KEYWORDS: Bonelli'sEagle,, Hieraaetus fasciatus; southeastern Spain; cliff selection; breeding density. Selecci6nde losroquedos de nidificaci6ndel Aguila Perdicera (Hieraaetus fasciatus) en el Surestede Espafia R•SUMEN.--119nidos y 52 roquedosocupados por 32 parejas de Aguila Perdicera (Hieraaetusfasdatus), fueronanalizados en el periodo1995-97 en el surestede Espafia.E1 nfimero medio de nidosconstruidos por pareja fue mayor que el descrito por otros autores (i = 3,7; N = 32). Los resultadosrevelan una tendenciade las /tguilasde construirsus nidos hacia la orientaci6n sureste.La densidadde parejas reproductorasestuvo directamente relacionada con la disponibilidadde roquedos.Los roquedosselec- cionadospara nidificar fueron de mayor altura (i = 52,9 m; N = 32), y ubicadossobre laderasde mayor pendiente (i = 34,7ø;N = 31), que la media disponible.Existi6 una gran versatilidadentre parejasen cuantoal tipode roquedoocupado, debido a queel AguilaPerdicera nidific6 en fireas muy diferentesen funci6n de la presi6n humana. De estaforma, los roquedosocupados m/rs pr6ximos a carreterastuvieron una altura mayor que los que se encontrabanlejos de las mismas.La selecci6nde roquedosde gran altura, situadossobre pendientes elevadas, y con orientaci6nsur, podria estarrela- cionadocon la faltade sustentaci6nen vuelo del Aguila Perdicera, al favorecereste tipo de roquedos la formaci6n de t6rmicasy el vuelo de ladera. La preservaci6nde los roquedosde nidificaci6nlibres de la influenciaantr6pica, podria ser la medidamils esencial requerida para la conservaci6ndelAguila Perdicera en el/trea de estudio. [Traducci6n de Autores] Among Mediterranean raptors, the Bonelli's Ea- has decreased25% from 1980-90 (Arroyo et al. gle (Hieraaetusfasdatus) has suffered one of the 1995). Consequently,this specieshas been cata- most severepopulation declinesin Spain (Fern•tn- logued as Vulnerable in Spain (Blanco and Gon- dez and Insausti1990, Real et al. 1991), Portugal z•lez 1992), and high-priority conservation has (Palma et al. 1984), France (Cugnase 1984, Chey- been urged (De Juana 1992). lan and Simeon 1985) and Greece (Hallmann Information concerning habitat is fundamental 1985) that have resulted in its being listed as an for the management of raptor populations(Mosh- Endangered European Raptor (Rocamora 1994). er et al. 1987). Raptorsare amongthe few groups Recent data indicate that the principal European of birds whose numbers can be limited by the avail- breeding population (80%) is located in Spain ability of appropriate nesting places (Newton (Real et al. 1997), where the nestingpopulation 1979). In Spain, Bonelli'sEagles most frequently 110 JUNE 1999 CLIFFSELECTION BY BONELLI'S EAGLES 111 Table 1. Variables used to characterize Bonelli's Eagle nest-sites. CLIFFNEST--number of cliffs with nestsbuilt by a pair NESTBUIL•number of nestsbuilt by a pair DISTNEST--greatest distancebetween nestsbelonging to the same pair (m) HEIGBAS•height from the base of the cliff to the nest (m) NEIGDIST--nearest-neighbor distancebetween adjacent pairs of Bonelli's Eagles (km) AVACLIFF--availabilityof clifi• (percentageof 1 km9 squareswith suitablecliffs for nestingin each territory) nest in cliffs and rarely in trees (Arroyo et al. A total of 119 nests located on 52 cliffs that were used 1995). While some aspectsof the biology of this by 32 different pairs of Bonelli's Eagle was studied. Rap- tors frequently build more than one nest and use them raptor are well-studied, nest-siteselection has re- alternately in different years (Newton 1979). Thus, all ceived only limited study.The two main studiesin nests (regardlessof whether they were occupied or not Spain (Gil-S•tnchezet al. 1996, Sgnchez-Zapataet during the present study) were considered equally for al. 1996) refer to the selection and characteristics the analysisif they were in occupied territories. of used and unused territories. No detailed infor- The variablesused in the analysisof nest-sitecharac- teristicsare defined in Table 1. The nearest-neighbordis- mation is available concerning the choice of nest tance method from the last nest used was used to est•- siteswithin territories or characteristicsof nesting mate breeding densityof the pairs (Newton et al. 1977). cliffs (Donfizar et al. 1989). For the analysisof cliff selection, 32 occupied cliffs The aim of my study was to determine which (last cliff used for nesting by each pair) were compared cliffs in each territory were used for nestingof Bo- with 32 unoccupied cliffs within the territories (one cliff per territory). The comparativeanalysis was performed nelli's Eagles, to describe characteristicsof cliff with variables to characterize the cliffs and human dis- nestingsites, and to determine how human activity turbm•ce in surrounding cliffs (Table 2). Because most affectsthis selectionin southeasternSpain. pairs built nestsin the highest cliff of each territory, the comparison was made with the highest unoccupied cliff STUDY AREA AND METHODS suitable for nestingwithin each territory. I considereda The studywas conducted in the province of Granada, cliff suitable for nesdngwhen there were suitable cavities southeasternSpain (36ø45'-37ø49'N,2ø40'-4ø13'W) from and ledges for nesting, when it was located at <1500 m 1995-97. The area is largely mountainouswith altitudes elevation (the distributional limit of the Spanishpopu- ranging from 0-3482 m, and highly variable tempera- lation, Arroyo et al. 1995), when it was higher than 10 tures and rainfall. The vegetation includes different spe- m, and farther than 500 m from an urban center (min- cies of pines (Pinus spp.) and evergreen oaks (Quercus imal distancesfound for the population studied). I chose •/ex) mixed with cultivated areas,mainly with olive trees the unoccupiedcliffs within each territory to eliminate (Olea europaea)and cereals (Rivas-Martinez1985). the possibilitythat limited prey availabilitywas the reason Table 2. Variablesused to characterizeoccupied and unoccupied cliffs in territories used by Bonelli's Eagles. ALTITUDE--height abovesea level measuredin the middle of the cliff (m) HEIGCLIFF--cliff height (m) HEIGVAL-•height from the bottom of the valleyto the baseof the cliff (m) HEIGHILEV--height from the upper edge of the cliff to the summit of a hill located on the cliff (m) WIDTHVAL width of the valleyat the baseof the cliff (m) SLOPE--inclination of the slope located at the base of the cliff (ø) TOPIND--topographic irregularityindex (total number of 20 m contour lines, cut by two lines equivalentto 2 km designedon topographic1:50 000 maps,in directionsN-S and E-W, and crossedat the location of the cliff) DISVIL•distance from cliff to nearest urban center (m) DISPAVROAD--distancefrom cliff to the nearestpaved road (m) DISUNPAVROAD--distancefrom cliff to the nearestunpaved road passableby vehicle (m) DISINHABUIL---distance from cliff to the nearestinhabited building (m) DISCULT1V--distance from cliff to the nearest cultivated field (m) KMPAVROAD--km of paved roads in the circular sampling area to the nearest 2 km KMUNPAVROAD--km of unpaved roads in the circular sampling area to the nearest 2 km 112 ONTIVEROS VOL. 33, NO. 2 Table 3. Means, standard deviations (SD) and ranges of tionship between variables. For occupied and unoccu- variables characterizing nest sites. pied cliffs, the mean values of the variables were com- pared using paired t-tests.As is usual in this type of analysis (Gonzalez et al. 1992, Penteriani and Faivre VARIABLE MEAN SD RANGE 1997),a stepwisediscriminant function analysis was con- CLIFFNEST 1.6 0.9 1-5 ducted (STATISTICA statsoftInc. 1993). The 0.05% level of significancewas used for including variablesin each NESTBUIL 3.7 3.6 1-18 step of the analysis.Because the sample size could not be DISTNEST 774.1 897.7 1-2800 increased to three times the number of variables mea- HEI GBAS 29.8 18.3 5-90 sured (Willians and Titus 1988), a jackknifed classifica- NEIGDIST 10.0 3.2 5.8-16 tion wasobtained for the analysis. AVACLIFF 10.0 4.3 4.7-22 RESULTS Most of the cliffs occupied by Bonelli's Eagles the cliff was unoccupied given that food availabilitydi- (96%, N = 50) were in river valleysand
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).
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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
    [Show full text]
  • 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.
    [Show full text]
  • FOOD of the BOOTED EAGLE &Lpar;<I>HIERAAETUS PENNATUS</I
    FOOD OF THE BOOTED EAGLE (HIERAAETUS PENNATUS) IN CENTRAL SPAIN JoskP. VEIGA ABSTRACT.m The identificationof 202 prey remainsof the BootedEagle (Hieraaetus pennatus) shows that mammals (41.6%of preyitems identified), birds (36.6%) and reptiles(21.8%) are importantprey in CentralSpain. Most mammals capturedwere youngrabbits, and the majorityof the bird prey were fledglingsor juveniles.Lizards were adult or subadultindividuals. Over 90% of the preycaptured weighed between 27 and 243 g. Little is known about the biologyof the Booted but no eagleswere seen in 1981.Visits were made approximately Eagle(Hieraaetus pennatus), as it occursin countries every 15 d from shortlybefore incubation (mid-late April) until after the youngleft the nest(mid-late August). During the feeding with little ornithologicalactivity. Most published periodnests were occasionallyvisited every 7 d. Pelletsand prey accountsof food habitsare singleenumerations of remainswere sought in andaround nests and below perches which prey remainsrecorded mainly during sporadicvis- were usuallywithin a 200 m radiusof the nests. its to nests(Valverde 1967; Arafijo 1973; Garz0n A total of 110 pellets,containing 130 identifiableprey items, 1973;Iribarren ! 975). This procedureprovides an and72 preyremains were collected. Each species found in anyone pelletwas counted as 1 individualunless it waspossible to show inaccuratepicture of diet, sinceprey that are large that more than 1 wasrepresented. Therefore, it wasnecessary to and leave persistentremains are over-represented countpieces of remainssuch as nails, beaks, teeth, etc. Weight and in samples(e.g., Valverde 1967;Delibes 1975). In approximateage of the prey were estimatedby comparingre- spiteof this, severalrecent papers dealing with the mainswith materialfrom zoologicalcollections and with speci- menscollected in the studyareas.
    [Show full text]
  • Hieraaetus) Weiskei (Accipitriformes: Accipitridae
    Zootaxa 2326: 24–38 (2009) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2009 · Magnolia Press ISSN 1175-5334 (online edition) Taxonomy and distribution of the Pygmy Eagle Aquila (Hieraaetus) weiskei (Accipitriformes: Accipitridae) JAN O. GJERSHAUG¹, HEATHER R.L. LERNER² & OLA H. DISERUD¹ ¹Norwegian Institute for Nature Research, Tungasletta 2, 7485 Trondheim, Norway. E-mail: [email protected]; [email protected] ²Smithsonian Institution, Center for Conservation and Evolutionary Genetics, National Zoological Park, Genetics Lab, 3001 Connecticut Avenue, NW, Washington, D.C. 20008, USA. E-mail: [email protected] Abstract We re-evaluated the taxonomic status of the New Guinean subspecies weiskei of the Little Eagle Aquila morphnoides and confirmed that it differs considerably from the Australian A. morphnoides in multiple morphological and plumage characters. Genetic differentiation in published mitochondrial cyt-b and ND2 sequences between the nominate subspecies and weiskei is equivalent to that found between other accipitrid taxa at the species level, as are pairwise divergences between each Little Eagle taxon and their sister species, the Booted Eagle A. pennata. The available morphological and genetic evidence thus strongly and unambiguously supports the specific distinctness of A. weiskei. We propose the English name Pygmy Eagle, as this is the world’s smallest known eagle. We show that the distribution of A. weiskei includes the western part of New Guinea (Vogelkop) and the Moluccas (Halmahera, Ternate and Seram), based on our new observations. Key words: morphology, genetics, pennata, morphnoides, Little Eagle, New Guinea, Moluccas Introduction The Little Eagle Aquila morphnoides was described by Gould (1841) from Australia.
    [Show full text]
  • New Host Records for Parasitic Mites of the Family Syringophilidae from Accipitriform Birds (Aves: Accipitriformes)
    Annals of Parasitology 2015, 61(4), 291–293 Copyright© 2015 Polish Parasitological Society doi: 10.17420/ap6104.21 Short notes New host records for parasitic mites of the family Syringophilidae from accipitriform birds (Aves: Accipitriformes) Mateusz Zmudzinski 1, Markus Unsoeld 2, Wayne Knee 3, Maciej Skoracki 1 1Department of Animal Morphology, Faculty of Biology, Adam Mickiewicz University, Umultowska 89, 61-614 Poznań, Poland 2Ornithological Section, Bavarian State Collection of Zoology, Muenchhausenstrasse 21, 81247 Munich, Germany 3Canadian National Collection of Insects, Arachnids and Nematodes, Agriculture and Agri-Food Canada, 960 Carling Avenue, Ottawa, Ontario, Canada K1A 0C6 Corresponding author: Maciej Skoracki; e-mail: [email protected] ABSTRACT. Four accipitriform bird species of the family Accipitridae are reported as new hosts for quill mites (Acari: Cheyletoidea: Syringophilidae): Megasyringophilus aquilus Skoracki, Lontkowski and Stawarczyk, 2010 was collected from Hieraaetus pennatus Gmelin, 1788 in France and Spain, and Buteo jamaicensis Gmelin, 1788 in Canada; Peristerophila accipitridicus Skoracki, Lontkowski and Stawarczyk, 2010 was collected from Circaetus gallicus Gmelin, 1788 in France, and Buteo lagopus Pontoppidan, 1763 in Germany. Key words: Acari, Accipitridae, birds, ectoparasites, quill mites Introduction on Accipiter nisus Linnaeus, 1758 from Kazakhstan [3] and on Terathopius ecaudatus Daudin, 1800 [4] Quill mites are permanent, obligatory, mono- or from unknown locality in Africa. oligoxenous parasites
    [Show full text]
  • Breeding of the Booted Eagle Hieraaetus Pennatus in North-Western Croatia Zwergadler-Brutvorkommen in Nordwest-Kroatien
    Delic & Muzinic:Booted © Eagle Ornithologische in Croatia Gesellschaft Bayern, download unter www.biologiezentrum.at 219 Orn Verh. 25: 219-222 Breeding of the Booted Eagle Hieraaetus pennatus in North-Western Croatia Zwergadler-Brutvorkommen in Nordwest-Kroatien By Antun Delic & Jasmina Muzinic 1. Introduction Although the Booted Eagle,Hieraaetus 1985). However, these data may insufficient pennatus, is a Mediterranean species (Ruc- to characterize the real state of the species’ ner 1968) it occurs as a breeding bird more distribution. frequently in the Southern and eastern parts A young Booted Eagle was found in the of the Balkan Peninsula than in Croatia Bilogora Mountain in Northwestern Croa­ (MATVEJEvet al. 1973). In Croatia the Booted tia at the utmost western fringe of its main Eagle is considered to be a breeding species breeding ränge in the East (Voous, 1960). only in Slavonia (= Slavonija, north-eastern The data concerning this record are pre- Croatia) (M atvejev et al. 1973; V asic et al. sented in this paper. 2. Area and Circumstances Bilogora is an elongated, wooded moun- The area where the bird was found is not tain ränge in the north-western part of settled by people, and the nearest village is Croatia (Fig. 1). It stretches from Kopriv- Turcevic Polje, about 2 km away in the bee nica on the west to Miokovicevo in the east. line. The highest peak of Bilogora is Rijeka, 307 The young Booted Eagle was found on m above sea level. 25th September 1992 by a forester. It was a A Booted Eagle nestling was found in thesunny and quiet day (the summer of 1992 is Veliki Rastovac Forest on the eastern slopes considered the hottest summer in the past of Bilogora at 232 m above sea level.
    [Show full text]
  • Kenya National Biodiversity Threat Assessment
    Kenya National Biodiversity Threat Assessment Direct Human Threats Impacting Kenya’s Biodiversity 1st September 2020 The report was prepared by Masumi S. Gudka for IUCN – BIODEV2030 Contents Acknowledgements ........................................................................................................................ c Abbreviations and Acronyms ........................................................................................................ e Executive Summary ........................................................................................................................ 1 Introduction ................................................................................................................................... 1 Methodology, Results & Analyses ................................................................................................. 1 Conclusion & Recommendations................................................................................................... 3 1. Introduction ................................................................................................................................. 5 1.1 BIODEV2030: Mainstreaming Biodiversity into Key Economic Sectors ................................... 5 1.2 BIODEV2030: Supporting Kenya Vision 2030 ......................................................................... 6 1.3 Purpose of the Assessment ..................................................................................................... 8 2. Methodology ..............................................................................................................................
    [Show full text]
  • Type-Specimens of Birds in the National Museum of Natural History, Leiden
    Type-specimens of birds in the National Museum of Natural History, Leiden Part 1. Non-Passerines L.W. van den Hoek Ostende, R.W.R.J. Dekker & G.O. Keijl Hoek Ostende, L.W. van den, R.W.R.J. Dekker & G.O. Keijl. Type-specimens of birds in the National Museum of Natural History, Leiden. Part 1. Non-Passerines. NNM Tech. Bull. 1, 30.xii.1997: 1-248— ISSN 1387-0211. Lars W. van den Hoek Ostende, National Museum of Natural History, P.O. Box 9517, 2300 RA, Leiden, The Netherlands. René W.R.J. Dekker, National Museum of Natural History, P.O. Box 9517, 2300 RA, Leiden, The Netherlands. Guido O. Keijl, National Museum of Natural History, P.O. Box 9517, 2300 RA, Leiden, The Netherlands. Key words: Aves; non-passerines; types; National Museum of Natural History; Rijksmuseum van Natuurlijke Historie; Nationaal Natuurhistorisch Museum. The non-Passerine type-specimens present in the National Museum of Natural History, Leiden, are listed. The history of the bird collection is summarized. Contents Contents ...................................................................................................................................3 Introduction .............................................................................................................................3 The history of the Leiden collection: important names ....................................................4 How to use this catalogue .....................................................................................................9 List of type-specimens .........................................................................................................11
    [Show full text]