Kestrels in the Karoo an Zyl Tographs Anthony V Text & Pho
Total Page:16
File Type:pdf, Size:1020Kb

Load more
Recommended publications
-
American Kestrel, Falco Sparverius
American Kestrel, Falco sparverius Status: State: Threatened Federal: Not listed Identification The American kestrel is the smallest and most widely distributed falcon in North America (Smallwood & Bird 2002, Hawk Mountain n.d.). At first glance, kestrels are often confused with other small birds such as mourning doves because of their propensity to perch on utility lines (Hawk Mountain n.d.). Kestrels however, have larger more roundish heads and often tip or “bob” their tails while perched. In flight, kestrels have a diagnostic flight pattern of quickly alternating between rapid wing beating and gliding. With proper lighting, their colorful plumage can further aid in positive identification. Kestrels are both sexually dimorphic and dichromatic; therefore sexing can be done at a distance and in chicks as young as three weeks (Hawk Mountain n.d.). Males are on average 10% smaller than females though this may be hard to ascertain in the field (Hawk Mountain 1997, Smallwood & Bird 2002). Males are more colorful, with bluish- gray wings (with or without black barring) and rufous (reddish-brown) tails. A single black bar tipped in white extends across the terminal end of the largely unmarked tail. Females are rufous on their wings and tails, often with multiple black bars extending horizontally along the length (Hawk Male American Kestrel Mountain n.d.). Plumage is highly variable © Jim Gilbert among individuals (Smallwood & Bird 2002). Both sexes exhibit grayish crowns and rufous crown patches with two vertical black stripes down their white cheeks. Black “eyespots on the back of their heads are thought to aid in reducing predation on kestrels by larger birds of prey- giving the illusion of predator awareness. -
Fascinating Falcons
48 Fascinating Falcons Falcons, worshipped as the "Lofty Ones," appeared in the writings, paintings, and sculptures of the early Egyptians and Persians some 3,000 years ago. References to the grace and power of falcons appeared during the times of Aristotle and Marco Polo. During the Middle Ages, owning falcons, particularly peregrine falcons, became a symbol of power. Peregrines were sought by kings and other nobility as valuable gifts. Falcons are swift birds of prey found throughout the world, except for a few oceanic islands and Antarctica. The 58 species of the falcon family range in size from the 6.5-inch pygmy falcon of South America to the 25-inch gyrfalcon of the Arctic tundra. The smallest North American falcon is the 9 to 12-inch American kestrel, and the rarest North American falcon is the aplamado falcon. Members of the falcon family have a conspicuous notched bill which is used to break the necks of their prey. Falcons have excellent eyesight. Experiments in Germany confirmed that peregrine falcons can recognize sitting doves from a distance up to 1.5 miles. With high-speed adaptations such as bullet-like heads, short necks, broad shoulders, and long, pointed wings, falcons are among the fastest birds in the world. Peregrines are considered the fastest falcons; they are able to cruise in level flight at 50-60 miles an hour and have been clocked at more than 200 miles per Peregrine Falcon hour in their dives after prey. The peregrine falcon's speed and grace make it one of the most interesting falcons to watch or study. -
Autumn Migration of an Amur Falcon Falco Amurensis from Mongolia to the Indian Ocean Tracked by Satellite ANDREW DIXON, NYAMBAYAR BATBAYAR and GANKHUYAG PUREV-OCHIR
Forktail 27 (2011) SHORT NOTES 81 because they showed: a relatively long, conical bill; heavily chestnut- Dymond, N. (1999) Two records of Black-headed Bunting Emberiza tinged uppertail-coverts and rump; and a dark crown. All three birds melanocephala in Sabah: the first definite occurrence in Malaysia and were aged as immature on account of their pale yellow undertail- Borneo. Forktail 15: 102–103. coverts, fawn underparts and worn yellowish flanks. Earlier published Grewal, B., Harvey, B. & Pfister, O. (2002) Birds of India including Nepal, Sri checklists for Bangladesh list four Emberiza species (see above), but Lanka, the Maldives, Pakistan, Bangladesh and Bhutan . London: none mentions E. melanocephala; hence it can be considered a new Christopher Helm. species for Bangladesh. Grimmett, R., Inskipp, C. & Inskipp, T. (1998) Birds of the Indian Subcontinent . Black-headed Bunting breeds in the western Palaearctic and Iran. London: Christopher Helm. It winters mainly in cultivated fields in southern Pakistan, west and Harvey, W. G. (1990) Birds in Bangladesh . Dhaka: University Press. central India and infrequently eastern Nepal and eastern India, with Husain, K. Z. (1979) Birds of Bangladesh . Dhaka: Government of Bangladesh. a few recent records from Jalpaiguri, West Bengal (S. Sen pers. comm. IUCN Bangladesh (2000) Red book of threatened birds of Bangladesh . Dhaka: 2011). It has a known tendency to vagrancy further east with records IUCN. from South-East Asia in north-west, central and southern Thailand, Khan, M. A. R. (1982) Wildlife of Bangladesh: a checklist . Dhaka: University of Singapore, northern Laos, northern Vietnam (Byers et al. 1995, Dhaka. Rasmussen & Anderton 2005, Robson 2008), southern China, Japan Khan, M. -
Rock Kestrel
264 Falconidae: falcons and kestrels brooding young. Therefore the small increase in reporting rates in six of the eight Zones during winter is probably related to seasonal changes in conspicuousness, rather than to any large- scale influx of migrants from outside the region. Reporting rates for the Tarkastad district, for example, increased during winter, while direct observation showed that over half of the population actually left the area (Van Zyl 1994b). Although the models do not suggest movements within southern Africa, a more detailed analysis of Rock Kestrel movements in South Africa, largely based on a more refined examination of atlas reporting rates, suggested a northerly and easterly movement away from south- western breeding areas during winter (Van Zyl et al. 1994). Breeding: Breeding was recorded in all Zones, mainly September–January, peaking October–December. There are no obvious seasonal differences between the Zones, although in the eastern Cape Province (Zone 8) it bred slightly later than in the rest of the region. Interspecific relationships: It overlaps widely with Greater and Lesser Kestrels in southern Africa. It moves into the eastern grassland habitats most exploited by the Lesser Kestrel during the winter when that species is absent (Van Zyl et al. 1994). Historical distribution and conservation: Boshoff et al. (1983) found no difference in distribution in the Cape Prov- ince, comparing the periods 1700–1969 and 1970–79. The distrib- ution map similarly shows no change in distribution, the species being largely absent from the central Kalahari regions and the far northeast during all three time periods, although the map shows Rock Kestrel many more records from the western Karoo, presumably due to Rooivalk better coverage. -
Migratory Connectivity and Conservation of the Amur Falcon Falco Amurensis: a Stable Isotope Perspective
Bird Conservation International (2010) 20:134–148. ª BirdLife International, 2010 doi:10.1017/S0959270910000237 Migratory connectivity and conservation of the Amur Falcon Falco amurensis: a stable isotope perspective CRAIG T. SYMES and STEPHAN WOODBORNE Summary 13 15 Stable isotopes (dD, d C, d N) were measured in adult and juvenile Amur Falcon Falco amurensis feathers to understand the migratory connectivity of this species. Using the OIPC (Online Isotopes in Precipitation Calculator) and a calibration curve for American Kestrels Falco sparverius we predicted the breeding range of South African Amur Falcons in the Palaearctic. dD values for juvenile feathers (mean 6 SE 5 À58.1 6 2.5&, range À83.9 to À25.7&) and predicted Palaearctic annual precipitation values indicated that juvenile Amur Falcons in South Africa originated from across their entire Palaearctic range. This rejects the leapfrog migration hypothesis and suggests the widespread movement of birds south, with a funnelling effect into the subregion where they become concentrated over a narrower distribution range. Adult dDf values were more depleted (À37.4 6 1.8&, range 5 À71.3 to À9.3&) than predicted annual precipitation values for sites where feathers moulted in South Africa (À20.2 6 0.9&) but there 13 was no correlation between dDp and dDf. This, together with significant variation of d C among sites and annual fluctuations in roost sizes, suggests that roost site fidelity is low in the overwintering range. Populations not confined to breeding sites in South Africa are able to move widely across the subregion, feeding on a broad range of arthropods that become seasonally abundant during the austral summer. -
New Insights Into the Phylogenetics and Population Structure of the Prairie Falcon (Falco Mexicanus) Jacqueline M
Doyle et al. BMC Genomics (2018) 19:233 https://doi.org/10.1186/s12864-018-4615-z RESEARCH ARTICLE Open Access New insights into the phylogenetics and population structure of the prairie falcon (Falco mexicanus) Jacqueline M. Doyle1,2*, Douglas A. Bell3,4, Peter H. Bloom5, Gavin Emmons6, Amy Fesnock7, Todd E. Katzner8, Larry LaPré9, Kolbe Leonard10, Phillip SanMiguel11, Rick Westerman11 and J. Andrew DeWoody2,12 Abstract Background: Management requires a robust understanding of between- and within-species genetic variability, however such data are still lacking in many species. For example, although multiple population genetics studies of the peregrine falcon (Falco peregrinus) have been conducted, no similar studies have been done of the closely- related prairie falcon (F. mexicanus) and it is unclear how much genetic variation and population structure exists across the species’ range. Furthermore, the phylogenetic relationship of F. mexicanus relative to other falcon species is contested. We utilized a genomics approach (i.e., genome sequencing and assembly followed by single nucleotide polymorphism genotyping) to rapidly address these gaps in knowledge. Results: We sequenced the genome of a single female prairie falcon and generated a 1.17 Gb (gigabases) draft genome assembly. We generated maximum likelihood phylogenetic trees using complete mitochondrial genomes as well as nuclear protein-coding genes. This process provided evidence that F. mexicanus is an outgroup to the clade that includes the peregrine falcon and members of the subgenus Hierofalco. We annotated > 16,000 genes and almost 600,000 high-quality single nucleotide polymorphisms (SNPs) in the nuclear genome, providing the raw material for a SNP assay design featuring > 140 gene-associated markers and a molecular-sexing marker. -
Syringeal Morphology and the Phylogeny of the Falconidae’
The Condor 96:127-140 Q The Cooper Ornithological Society 1994 SYRINGEAL MORPHOLOGY AND THE PHYLOGENY OF THE FALCONIDAE’ CAROLES.GRIFFITHS Departmentof Ornithology,American Museum of NaturalHistory and Departmentef Biology, City Collegeof City Universityof New York, Central Park West at 79th St., New York, NY 10024 Abstract. Variation in syringealmorphology was studied to resolve the relationshipsof representativesof all of the recognized genera of falcons, falconets, pygmy falcons, and caracarasin the family Falconidae. The phylogenyderived from thesedata establishesthree major cladeswithin the family: (1) the Polyborinae, containingDaptrius, Polyborus, Milvago and Phalcoboenus,the four genera of caracaras;(2) the Falconinae, consistingof the genus Falco, Polihierax (pygmy falcons),Spiziapteryx and Microhierax (falconets)and Herpetothe- res (Laughing Falcon); and (3) the genus Micrastur(forest falcons) comprising the third, basal clade. Two genera, Daptriusand Polihierax,are found to be polyphyletic. The phy- logeny inferred from these syringealdata do not support the current division of the family into two subfamilies. Key words: Falconidae;phylogeny; systematics; syrinx; falcons; caracaras. INTRODUCTION 1. The Polyborinae. This includes seven gen- Phylogenetic relationships form the basis for re- era: Daptrius, Milvago, Polyborus and Phalco- searchin comparative and evolutionary biology boenus(the caracaras),Micrastur (forest falcons), (Page1 and Harvey 1988, Gittleman and Luh Herpetotheres(Laughing Falcon) and Spiziapter- 1992). Patterns drawn from cladogramsprovide yx (Spot-winged Falconet). the blueprints for understanding biodiversity, 2. The Falconinae. This includes three genera: biogeography,behavior, and parasite-hostcospe- Falco, Polihierax (pygmy falcons) and Micro- ciation (Vane-Wright et al. 199 1, Mayden 1988, hierax (falconets). Page 1988, Coddington 1988) and are one of the Inclusion of the caracarasin the Polyborinae key ingredients for planning conservation strat- is not questioned (Sharpe 1874, Swann 1922, egies(Erwin 199 1, May 1990). -
Effects of Nest and Colony Features on Lesser Kestrel Survival
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Archivio istituzionale della ricerca - Università di Palermo Effects of nest and colony features on lesser kestrel (Falco naumanni) reproductive success Maurizio Sarà$, Daniela Campobello, Laura Zanca Dipartimento Biologia Ambientale e Biodiversità – Università di Palermo, Via Archirafi, 18 – 90123 Palermo, Italy $corresponding author: [email protected] ABSTRACT Lesser kestrel is a facultative colonial raptor mostly breeding in man-made structures. During 2009- 2011 we checked the fate of 545 nests found in 18 colonies located in south-eastern Sicily. We determined the reproductive success of breeding pairs by analysing the survival time of each egg to hatching (n = 2495) and each nestling to fledging (n = 1849) with the Linear Hazard model of survival times. We determined whether egg and nestling survival differed between years with a Gehan-Wilcoxon test. By Cox regressions, we related the survival times with nest and colony features. Egg and nestling survival times showed a strong annual effect. The two reproductive stages of lesser kestrel when controlled for the annual effect demonstrated a significant effect for some nest and colony features. Most of them, like height from the ground, nest depth, reused nests and the presence of jackdaws, are likely related to the predation pressure faced by lesser kestrel nests. Westward and southward nests had a better egg survival respect to those in the cold sides and in the interior of buildings. The location of colony in the agricultural plain and human disturbance ranked as the most important variables, with core location of a colony and high disturbance levels negatively affecting the reproductive success of lesser kestrel in the Gela Plain, so urging a more environment-aware land use management of this Important Bird Area. -
American Kestrel Mountain Region
United States Department of Agriculture Conservation Assessment Forest Service Rocky for the American Kestrel Mountain Region Black Hills in the Black Hills National National Forest Custer, Forest, South Dakota and South Dakota December 2002 Wyoming Aran S. Johnson and Stanley H. Anderson Conservation Assessment for the American Kestrel in the Black Hills National Forest, South Dakota and Wyoming. Aran S. Johnson and Stanley H. Anderson Wyoming Cooperative Fish and Wildlife Research Unit University of Wyoming P.O. Box 3166 Laramie, Wyoming 82071 Aran S. Johnson is a Research Scientist in the Wyoming Cooperative Fish and Wildlife Research Unit at the University of Wyoming. He received his B.Sc. in 1995 at the University of Wisconsin at Green Bay and his M.Sc. in 2001 at the University of Wyoming. His master’s project investigated logging effects on riparian and upland songbird species. Raptor projects that Aran has been involved with have included studies on Northern Harriers, American Kestrels, Northern Goshawks, Golden Eagles, Ferruginous Hawks and Burrowing Owls. Stanley H. Anderson is the leader of the Wyoming Cooperative Fish and Wildlife Research Unit. He received his Ph.D. from Oregon State University in 1970 and his B.Sc. from the University of Redlands in 1961. During his career at Kenyon College, Oak Ridge National Laboratories, Patuxent Research Center and the Wyoming Cooperative Fish and Wildlife Research Unit he has worked extensively on wildlife habitat, publishing as author or co-author more than 230 scientific articles. Stan has done extensive work on raptors throughout the United States, South America, and Australia. He has worked with nearly 100 graduate students at the Coop and presented courses in ornithology and wildlife management. -
1 Systematics and Evolution of Kestrels
Cambridge University Press 978-1-108-47062-9 — The Kestrel David Costantini , Giacomo Dell'Omo Excerpt More Information 1 Systematics and Evolution of Kestrels 1.1 Chapter Summary The family Falconidae constitutes a group of small to medium-sized diurnal raptors whose monophyly is strongly supported. Kestrels are included in the subfamily Falconinae. There are at least 13 species that belong to the kestrel group, but recent genetic studies suggest that the number of kestrel species might be larger, possibly 16. The paleontological and molecular evidence is congruent in suggesting an evolutionary radiation of kestrels from the Late Miocene (4.0–9.8 million years ago) through the Early Pleistocene. However, the geographic area where kestrels originated and dispersed from is unclear. 1.2 Diversification of Falcons The Falconidae is a monophyletic family of diurnal birds of prey that occupy a wide variety of ecological niches and geographic regions (White et al., 1994). Three subfamilies are currently recognised and their validity is supported by both molecular and morphological data (Griffiths, 1999; Griffiths et al., 2004; Fuchs et al., 2012, 2015): (i) Falconinae (falcons, falconets and kestrels), (ii) Herpetotherinae (forest falcons Micrastur sp. and laughing falcon Herpetotheres cachinnans) and (iii) Polyborinae (caracaras) (Figure 1.1). Dickinson (2003) has recognised 11 genera and 64 species of Falconidae, but figures can vary slightly across authors. Both the Herpetotherinae and the Polyborinae occur only in the New World, while the Falconinae (the subfamily to which kestrels belong) are widespread across both the New and Old World with 46 species, 40 of which belong to the genus Falco (Fuchs et al., 2015). -
Newsletter No 4
Page 1 of 4 NEWSLETTER NUMBER 4 September 2012 Hi all. Welcome to our fourth newsletter. We hope you find it as enjoyable and full of news as the last three. Saturday Morning Walks. Your Committee has decided to offer a series of informal “Summer Walks” to the vlei. The proposal is to meet once per month, during the summer months, on a Saturday morning from 07h00 onwards for an hour or two’s summer birding. The aims are multiple: - To observe the birds arrivals (migrants) and later in the season, their departure, - To observe the breeding habits of the birds, - To watch the development, including plumage changes in the young birds as they grow, and above all, - TO MEET FELLOW BIRDERS, ENJOY OUR HOBBY AND SHARE OUR KNOWLEDGE! Posters were placed in various places around town giving details of the September “Summer Walk”, and we hope those attending enjoyed it. A brief report on the outing follows .Further Walks will be held as follows: October 6th 2012 November 3rd 2012 December 8th 2012 January 5th 2013 February 2nd 2013 March 2nd 2013 April - to be confirmed. These Saturday walks will be in addition to our normal monthly outings (where we go a little further afield) and are intended to be casual get-togethers with a view to pass around some knowledge and obviously the beginners will be given every assistance ! Page 2 of 4 Outing to the Vlei – 15 September 2012 Considering the inclement weather, we had a good turn out to the first of the monthly trips to the Vlei. -
Tafila Region Wind Power Projects Cumulative Effects Assessment © International Finance Corporation 2017
Tafila Region Wind Power Projects Cumulative Effects Assessment © International Finance Corporation 2017. All rights reserved. 2121 Pennsylvania Avenue, N.W. Washington, D.C. 20433 Internet: www.ifc.org The material in this work is copyrighted. Copying and/or transmitting portions or all of this work without permission may be a violation of applicable law. IFC encourages dissemination of its work and will normally grant permission to reproduce portions of the work promptly, and when the reproduction is for educational and non-commercial purposes, without a fee, subject to such attributions and notices as we may reasonably require. IFC does not guarantee the accuracy, reliability or completeness of the content included in this work, or for the conclusions or judgments described herein, and accepts no responsibility or liability for any omissions or errors (including, without limitation, typographical errors and technical errors) in the content whatsoever or for reliance thereon. The boundaries, colors, denominations, and other information shown on any map in this work do not imply any judgment on the part of The World Bank concerning the legal status of any territory or the endorsement or acceptance of such boundaries. The findings, interpretations, and conclusions expressed in this volume do not necessarily reflect the views of the Executive Directors of The World Bank or the governments they represent. The contents of this work are intended for general informational purposes only and are not intended to constitute legal, securities, or investment advice, an opinion regarding the appropriateness of any investment, or a solicitation of any type. IFC or its affiliates may have an investment in, provide other advice or services to, or otherwise have a financial interest in, certain of the companies and parties (including named herein.