Southern Tanzania: Endemic Birds & Spectacular Mammals
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SINGITA SABI SAND, SOUTH AFRICA for the Month of December, Two Thousand and Fifteen
WILDLIFE REPORT SINGITA SABI SAND, SOUTH AFRICA For the month of December, Two Thousand and Fifteen Temperature Rainfall Recorded Sunrise & Sunset Average minimum: 22˚C (71.6˚F) For the month: 36 mm Sunrise 05:05 Average maximum: 34.2˚C (93.6˚F) For the year to date: 286 mm Sunset 18:46 Minimum recorded: 18◦C (64.4˚F) For the season to date: 173.2 mm Maximum recorded: 41˚C (105.8˚F) With a maximum record of 41˚C, the vegetation has been scorched by the hot conditions. Fortunately with the light rain that we did receive it’s allowed some of the flowering plants to blossom. Here's a highlights package of the month's sightings: Hyenas: It's such a joy when hyena cubs are about - they're curios and like to investigate everything around them. Lions: Lion sightings currently could not get any better! Two male lions of the Matimba coalition have been sighted on a few occasions, and they are gradually expanding their current territorial zone north of the river. The Mhangene pride continue to dominate the central area of Singita Sabi Sand. We watched a few interactions between the Majingalane male lions and the sub-adult males of the Mhangene pride that resulted in the young males being dispersed from the pride temporarily. One of the lionesses from the Mhangene pride has been seen with prominent suckle marks indicating that she has given birth. The lionesses has been seen moving in front of the lodges during the early morning and we suspect that the cubs are hidden in the river just east of Boulders Lodge. -
Comments on the Ornithology of Nigeria, Including Amendments to the National List
Robert J. Dowsett 154 Bull. B.O.C. 2015 135(2) Comments on the ornithology of Nigeria, including amendments to the national list by Robert J. Dowsett Received 16 December 2014 Summary.—This paper reviews the distribution of birds in Nigeria that were not treated in detail in the most recent national avifauna (Elgood et al. 1994). It clarifies certain range limits, and recommends the addition to the Nigerian list of four species (African Piculet Verreauxia africana, White-tailed Lark Mirafra albicauda, Western Black-headed Batis Batis erlangeri and Velvet-mantled Drongo Dicrurus modestus) and the deletion (in the absence of satisfactory documentation) of six others (Olive Ibis Bostrychia olivacea, Lesser Short-toed Lark Calandrella rufescens, Richard’s Pipit Anthus richardi, Little Grey Flycatcher Muscicapa epulata, Ussher’s Flycatcher M. ussheri and Rufous-winged Illadopsis Illadopsis rufescens). Recent research in West Africa has demonstrated the need to clarify the distributions of several bird species in Nigeria. I have re-examined much of the literature relating to the country, analysed the (largely unpublished) collection made by Boyd Alexander there in 1904–05 (in the Natural History Museum, Tring; NHMUK), and have reviewed the data available in the light of our own field work in Ghana (Dowsett-Lemaire & Dowsett 2014), Togo (Dowsett-Lemaire & Dowsett 2011a) and neighbouring Benin (Dowsett & Dowsett- Lemaire 2011, Dowsett-Lemaire & Dowsett 2009, 2010, 2011b). The northern or southern localities of species with limited ranges in Nigeria were not always detailed by Elgood et al. (1994), although such information is essential for understanding distribution patterns and future changes. For many Guineo-Congolian forest species their northern limit in West Africa lies on the escarpment of the Jos Plateau, especially Nindam Forest Reserve, Kagoro. -
Species List
Mozambique: Species List Birds Specie Seen Location Common Quail Harlequin Quail Blue Quail Helmeted Guineafowl Crested Guineafowl Fulvous Whistling-Duck White-faced Whistling-Duck White-backed Duck Egyptian Goose Spur-winged Goose Comb Duck African Pygmy-Goose Cape Teal African Black Duck Yellow-billed Duck Cape Shoveler Red-billed Duck Northern Pintail Hottentot Teal Southern Pochard Small Buttonquail Black-rumped Buttonquail Scaly-throated Honeyguide Greater Honeyguide Lesser Honeyguide Pallid Honeyguide Green-backed Honeyguide Wahlberg's Honeyguide Rufous-necked Wryneck Bennett's Woodpecker Reichenow's Woodpecker Golden-tailed Woodpecker Green-backed Woodpecker Cardinal Woodpecker Stierling's Woodpecker Bearded Woodpecker Olive Woodpecker White-eared Barbet Whyte's Barbet Green Barbet Green Tinkerbird Yellow-rumped Tinkerbird Yellow-fronted Tinkerbird Red-fronted Tinkerbird Pied Barbet Black-collared Barbet Brown-breasted Barbet Crested Barbet Red-billed Hornbill Southern Yellow-billed Hornbill Crowned Hornbill African Grey Hornbill Pale-billed Hornbill Trumpeter Hornbill Silvery-cheeked Hornbill Southern Ground-Hornbill Eurasian Hoopoe African Hoopoe Green Woodhoopoe Violet Woodhoopoe Common Scimitar-bill Narina Trogon Bar-tailed Trogon European Roller Lilac-breasted Roller Racket-tailed Roller Rufous-crowned Roller Broad-billed Roller Half-collared Kingfisher Malachite Kingfisher African Pygmy-Kingfisher Grey-headed Kingfisher Woodland Kingfisher Mangrove Kingfisher Brown-hooded Kingfisher Striped Kingfisher Giant Kingfisher Pied -
Systematic Notes on Asian Birds. 28
ZV-340 179-190 | 28 04-01-2007 08:56 Pagina 179 Systematic notes on Asian birds. 28. Taxonomic comments on some south and south-east Asian members of the family Nectariniidae C.F. Mann Mann, C.F. Systematic notes on Asian birds. 28. Taxonomic comments on some south and south-east Asian members of the family Nectariniidae. Zool. Verh. Leiden 340, 27.xii.2002: 179-189.— ISSN 0024-1652/ISBN 90-73239-84-2. Clive F. Mann, 53 Sutton Lane South, London W4 3JR, U.K. (e-mail: [email protected]). Keywords: Asia; Nectariniidae; taxonomy. Certain taxonomic changes made by Cheke & Mann (2001) are here explained and justified. Dicaeum haematostictum Sharpe, 1876, is split from D. australe (Hermann, 1783). D. aeruginosum Bourns & Worcester, 1894 is merged into D. agile (Tickell, 1833). The genus Chalcoparia Cabanis, 1851, is re-estab- lished for (Motacilla) singalensis Gmelin, 1788. The taxon Leptocoma sperata marinduquensis (duPont, 1971), is shown to be based on a specimen of Aethopyga siparaja magnifica Sharpe, 1876. Aethopyga vigor- sii (Sykes, 1832) is split from A. siparaja (Raffles, 1822). Cheke & Mann (op. cit.) mistakenly omitted two forms, Anthreptes malacensis erixanthus Oberholser, 1932 and Arachnothera longirostra zarhina Ober- holser, 1912. Five subspecies are removed from Aethopyga shelleyi Sharpe, 1876 to create the polytypic A. bella, Tweeddale, 1877. The Arachnothera affinis (Horsfield, 1822)/modesta (Eyton, 1839)/everetti (Sharpe, 1893) complex is re-evaluated in the light of the revision by Davison in Smythies (1999). Introduction In a recent publication (Cheke & Mann, 2001) some taxonomic changes were made to members of this family occurring in Asia. -
STATUS SURVEY of AFRICAN GREEN PIGEON (Treroncalvus
STATUS SURVEY OF AFRICAN GREEN PIGEON (Treroncalvus, Temminck, 1808) IN EKITI STATE, NIGERIA BY OWOLABI, BIBITAYO AYOBAMI B. Wildlife Management (EWM/13/5440) A THESIS IN THE DEPARTMENT OF ECOTOURISM AND WILDLIFE MANAGEMENT, SUBMITTED TO THE SCHOOL OF POST GRADUATE STUDIES, THE FEDERAL UNIVERSITY OF TECHNOLOGY,AKURE, ONDO STATE. IN PARTIAL FULFILLMENT OF THE REQUIREMENT FOR THE AWARD OF THE DEGREE OF MASTER OF AGRICULTURAL TECHNOLOGY IN ECOTOURISM AND WILDLIFE MANAGEMENT. OCTOBER 2015. ABSTRACT The study focused on assessment and survey of thestatus survey of African Green Pigeon in EkitiState,Nigeria. Following the reconnaissance survey of the state, five sites were purposively selected, which represented areas where African Green Pigeon were commonly sighted. These areas were Counting station A (Aramoko/IjeroEkiti), Counting station B (IsanEkiti), Counting station C (IkogosiEkiti), Counting station D (Awo/IgedeEkiti) and Counting station E (IyemeroEkiti). The study area represents a typical rain forest ecosystem. Three methods were used for collecting data for the study (Point count method, direct observation and vegetation assessment technique). A meantotal of 97 birds were counted during the wet and dry season of the study, 46during the dry season and 51 counted during the wet season.Total mean number of bird in Counting Station A in the dry period was 10 and 9 in the wet season, accounting for a standard error of 3 ± 2.186birds sighted in the dry season and 3 ± 2.646in the wet season. Counting Station B forest patches, had a total of 29 birds, 9 sighted in the dry and 14 in the wet period, 3 ± 1.201 as standard error of birds sighted in the wet season and 3 ± 1.527 foe the dry season while counting Station C forest patches with 8 birds sighted in the dry and 12 birds recorded in the wet season, having a standard error of 3 ± 2.603 birds sighted in the dry and 3 ± 0.577 in the wet season. -
A Thesis Entitled Nocturnal Bird Call Recognition System for Wind Farm
A Thesis entitled Nocturnal Bird Call Recognition System for Wind Farm Applications by Selin A. Bastas Submitted to the Graduate Faculty as partial fulfillment of the requirements for the Master of Science Degree in Electrical Engineering _______________________________________ Dr. Mohsin M. Jamali, Committee Chair _______________________________________ Dr. Junghwan Kim, Committee Member _______________________________________ Dr. Sonmez Sahutoglu, Committee Member _______________________________________ Dr. Patricia R. Komuniecki, Dean College of Graduate Studies The University of Toledo December 2011 Copyright 2011, Selin A. Bastas. This document is copyrighted material. Under copyright law, no parts of this document may be reproduced without the expressed permission of the author. An Abstract of Nocturnal Bird Call Recognition System for Wind Farm Applications by Selin A. Bastas Submitted to the Graduate Faculty as partial fulfillment of the requirements for the Master of Science Degree in Electrical Engineering The University of Toledo December 2011 Interaction of birds with wind turbines has become an important public policy issue. Acoustic monitoring of birds in the vicinity of wind turbines can address this important public policy issue. The identification of nocturnal bird flight calls is also important for various applications such as ornithological studies and acoustic monitoring to prevent the negative effects of wind farms, human made structures and devices on birds. Wind turbines may have negative impact on bird population. Therefore, the development of an acoustic monitoring system is critical for the study of bird behavior. This work can be employed by wildlife biologist for developing mitigation techniques for both on- shore/off-shore wind farm applications and to address bird strike issues at airports. -
Dendroaspis Viridis
Dendroaspis viridis The western green mamba (Dendroaspis viridis), also known as the West African green mamba or Hallowell's green mamba, is a long, thin, and highly venomous snake of the mamba genus, Dendroaspis. This species was first described in 1844 by the American herpetologist Edward Hallowell. The western green mamba is a fairly large and predominantly arboreal species, capable of navigating through trees swiftly and gracefully. It will also descend to ground level to pursue prey such as rodents and other small mammals. The western green mamba is a very alert, nervous, and extremely agile snake that lives mainly in the coastal tropical rainforest, thicket, Scientific Classification and woodland regions of western Africa. Like all the other mambas, the western green mamba is a highly venomous elapid species. Its Kingdom: Anamalia venom is a highly potent mixture of rapid-acting presynaptic and Phylum: Cordata postsynaptic neurotoxins (dendrotoxins), cardiotoxins and fasciculins. Class: Reptilia Some consider this species to not be a particularly aggressive snake, Order: Squamata but others have suggested that they are extremely nervous and are Suborder: Serpentes prone to attack aggressively when cornered. Conflict with humans is Family: Elapidae low compared to some other species found in the region. Bites to Geunus Dendroaspis people by this species are quite uncommon. Their mortality rate, Species D.Viridis however, is high; many of the recorded bites have been fatal. Rapid progression of severe, life-threatening symptoms are hallmarks of Binomial Name mamba bites. Bites with envenomation can be rapidly fatal. Dendroaspis viridis (Hallowell, 1844)[2] Taxonomy Dendroaspis viridis was first described by the American herpetologist and physician Edward Hallowell in 1844.[2][5] In addition to being called the western green mamba, this species is also commonly known as [6] the West African green mamba or Hallowell's green mamba. -
The Birds (Aves) of Oromia, Ethiopia – an Annotated Checklist
European Journal of Taxonomy 306: 1–69 ISSN 2118-9773 https://doi.org/10.5852/ejt.2017.306 www.europeanjournaloftaxonomy.eu 2017 · Gedeon K. et al. This work is licensed under a Creative Commons Attribution 3.0 License. Monograph urn:lsid:zoobank.org:pub:A32EAE51-9051-458A-81DD-8EA921901CDC The birds (Aves) of Oromia, Ethiopia – an annotated checklist Kai GEDEON 1,*, Chemere ZEWDIE 2 & Till TÖPFER 3 1 Saxon Ornithologists’ Society, P.O. Box 1129, 09331 Hohenstein-Ernstthal, Germany. 2 Oromia Forest and Wildlife Enterprise, P.O. Box 1075, Debre Zeit, Ethiopia. 3 Zoological Research Museum Alexander Koenig, Centre for Taxonomy and Evolutionary Research, Adenauerallee 160, 53113 Bonn, Germany. * Corresponding author: [email protected] 2 Email: [email protected] 3 Email: [email protected] 1 urn:lsid:zoobank.org:author:F46B3F50-41E2-4629-9951-778F69A5BBA2 2 urn:lsid:zoobank.org:author:F59FEDB3-627A-4D52-A6CB-4F26846C0FC5 3 urn:lsid:zoobank.org:author:A87BE9B4-8FC6-4E11-8DB4-BDBB3CFBBEAA Abstract. Oromia is the largest National Regional State of Ethiopia. Here we present the first comprehensive checklist of its birds. A total of 804 bird species has been recorded, 601 of them confirmed (443) or assumed (158) to be breeding birds. At least 561 are all-year residents (and 31 more potentially so), at least 73 are Afrotropical migrants and visitors (and 44 more potentially so), and 184 are Palaearctic migrants and visitors (and eight more potentially so). Three species are endemic to Oromia, 18 to Ethiopia and 43 to the Horn of Africa. 170 Oromia bird species are biome restricted: 57 to the Afrotropical Highlands biome, 95 to the Somali-Masai biome, and 18 to the Sudan-Guinea Savanna biome. -
Tc & Forward & Owls-I-IX
USDA Forest Service 1997 General Technical Report NC-190 Biology and Conservation of Owls of the Northern Hemisphere Second International Symposium February 5-9, 1997 Winnipeg, Manitoba, Canada Editors: James R. Duncan, Zoologist, Manitoba Conservation Data Centre Wildlife Branch, Manitoba Department of Natural Resources Box 24, 200 Saulteaux Crescent Winnipeg, MB CANADA R3J 3W3 <[email protected]> David H. Johnson, Wildlife Ecologist Washington Department of Fish and Wildlife 600 Capitol Way North Olympia, WA, USA 98501-1091 <[email protected]> Thomas H. Nicholls, retired formerly Project Leader and Research Plant Pathologist and Wildlife Biologist USDA Forest Service, North Central Forest Experiment Station 1992 Folwell Avenue St. Paul, MN, USA 55108-6148 <[email protected]> I 2nd Owl Symposium SPONSORS: (Listing of all symposium and publication sponsors, e.g., those donating $$) 1987 International Owl Symposium Fund; Jack Israel Schrieber Memorial Trust c/o Zoological Society of Manitoba; Lady Grayl Fund; Manitoba Hydro; Manitoba Natural Resources; Manitoba Naturalists Society; Manitoba Critical Wildlife Habitat Program; Metro Propane Ltd.; Pine Falls Paper Company; Raptor Research Foundation; Raptor Education Group, Inc.; Raptor Research Center of Boise State University, Boise, Idaho; Repap Manitoba; Canadian Wildlife Service, Environment Canada; USDI Bureau of Land Management; USDI Fish and Wildlife Service; USDA Forest Service, including the North Central Forest Experiment Station; Washington Department of Fish and Wildlife; The Wildlife Society - Washington Chapter; Wildlife Habitat Canada; Robert Bateman; Lawrence Blus; Nancy Claflin; Richard Clark; James Duncan; Bob Gehlert; Marge Gibson; Mary Houston; Stuart Houston; Edgar Jones; Katherine McKeever; Robert Nero; Glenn Proudfoot; Catherine Rich; Spencer Sealy; Mark Sobchuk; Tom Sproat; Peter Stacey; and Catherine Thexton. -
South Africa: Magoebaskloof and Kruger National Park Custom Tour Trip Report
SOUTH AFRICA: MAGOEBASKLOOF AND KRUGER NATIONAL PARK CUSTOM TOUR TRIP REPORT 24 February – 2 March 2019 By Jason Boyce This Verreaux’s Eagle-Owl showed nicely one late afternoon, puffing up his throat and neck when calling www.birdingecotours.com [email protected] 2 | TRIP REPORT South Africa: Magoebaskloof and Kruger National Park February 2019 Overview It’s common knowledge that South Africa has very much to offer as a birding destination, and the memory of this trip echoes those sentiments. With an itinerary set in one of South Africa’s premier birding provinces, the Limpopo Province, we were getting ready for a birding extravaganza. The forests of Magoebaskloof would be our first stop, spending a day and a half in the area and targeting forest special after forest special as well as tricky range-restricted species such as Short-clawed Lark and Gurney’s Sugarbird. Afterwards we would descend the eastern escarpment and head into Kruger National Park, where we would make our way to the northern sections. These included Punda Maria, Pafuri, and the Makuleke Concession – a mouthwatering birding itinerary that was sure to deliver. A pair of Woodland Kingfishers in the fever tree forest along the Limpopo River Detailed Report Day 1, 24th February 2019 – Transfer to Magoebaskloof We set out from Johannesburg after breakfast on a clear Sunday morning. The drive to Polokwane took us just over three hours. A number of birds along the way started our trip list; these included Hadada Ibis, Yellow-billed Kite, Southern Black Flycatcher, Village Weaver, and a few brilliant European Bee-eaters. -
The Kavirondo Escarpment: a Previously Unrecognized Site of High Conservation Value in Western Kenya
Scopus 33: 64-69 January 2014 The Kavirondo Escarpment: a previously unrecognized site of high conservation value in Western Kenya James Bradley and David Bradley Summary In western Kenya, extant woodland habitats and their representative bird species are increasingly scarce outside of protected areas. With the assistance of satellite imagery we located several minimally impacted ecosystems on the Kavirondo Escarpment (0°1.7’ S, 34°56.5’ E), which we then visited to examine the vegetation communities and investigate the avifauna. Despite only a limited effort there, we report several new atlas square occurrences, presence of the local and poorly known Rock Cisticola Cisticola emini and a significant range extension for the Stone Partridge Ptilopachus petrosus. Our short visits indicate high avian species richness is associated with the escarpment and we suggest comprehensive biodiversity surveys here are warranted. Introduction The Kavirondo Escarpment in central-west Kenya is a significant geologic and topographic feature. It straddles the equator, extending over 45 km from east to west, and comprises the northern fault line escarpment of the Kavirondo Rift Valley (Baker et al. 1972). Immediately to the south lie the lowlands of the Lake Victoria Basin and Nyando River Valley, and to the north, the high plateau of the western Kenya highlands (Fig. 1). The escarpment slopes range in elevation from 1200–1700 m at the western end to 1500–2000 m in the east, where it gradually merges with the Nandi Hills. Numerous permanent and seasonal drainages on the escarpment greatly increase the extent of land surface and variation in slope gradients, as well as the richness of vegetation communities. -
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 .................................................................................................................................................................................................................................................