Standards for Ground Feeding Bird Sanctuaries
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A Baraminological Analysis of the Land Fowl (Class Aves, Order Galliformes)
Galliform Baraminology 1 Running Head: GALLIFORM BARAMINOLOGY A Baraminological Analysis of the Land Fowl (Class Aves, Order Galliformes) Michelle McConnachie A Senior Thesis submitted in partial fulfillment of the requirements for graduation in the Honors Program Liberty University Spring 2007 Galliform Baraminology 2 Acceptance of Senior Honors Thesis This Senior Honors Thesis is accepted in partial fulfillment of the requirements for graduation from the Honors Program of Liberty University. ______________________________ Timothy R. Brophy, Ph.D. Chairman of Thesis ______________________________ Marcus R. Ross, Ph.D. Committee Member ______________________________ Harvey D. Hartman, Th.D. Committee Member ______________________________ Judy R. Sandlin, Ph.D. Assistant Honors Program Director ______________________________ Date Galliform Baraminology 3 Acknowledgements I would like to thank my Lord and Savior, Jesus Christ, without Whom I would not have had the opportunity of being at this institution or producing this thesis. I would also like to thank my entire committee including Dr. Timothy Brophy, Dr. Marcus Ross, Dr. Harvey Hartman, and Dr. Judy Sandlin. I would especially like to thank Dr. Brophy who patiently guided me through the entire research and writing process and put in many hours working with me on this thesis. Finally, I would like to thank my family for their interest in this project and Robby Mullis for his constant encouragement. Galliform Baraminology 4 Abstract This study investigates the number of galliform bird holobaramins. Criteria used to determine the members of any given holobaramin included a biblical word analysis, statistical baraminology, and hybridization. The biblical search yielded limited biosystematic information; however, since it is a necessary and useful part of baraminology research it is both included and discussed. -
Sri Lanka: January 2015
Tropical Birding Trip Report Sri Lanka: January 2015 A Tropical Birding CUSTOM tour SRI LANKA: Ceylon Sojourn 9th- 23rd January 2015 Tour Leaders: Sam Woods & Chaminda Dilruk SRI LANKA JUNGLEFOWL is Sri Lanka’s colorful national bird, which was ranked among the top five birds of the tour by the group. All photos in this report were taken by Sam Woods. 1 www.tropicalbirding.com +1-409-515-0514 [email protected] Page Tropical Birding Trip Report Sri Lanka: January 2015 INTRODUCTION In many ways Sri Lanka covers it all; for the serious birder, even those with experience from elsewhere in the Indian subcontinent, it offers up a healthy batch of at least 32 endemic bird species (this list continues to grow, though, so could increase further yet); for those without any previous experience of the subcontinent it offers these but, being an island of limited diversity, not the overwhelming numbers of birds, which can be intimidating for the first timer; and for those with a natural history slant that extends beyond the avian, there is plentiful other wildlife besides, to keep all happy, such as endemic monkeys, strange reptiles only found on this teardrop-shaped island, and a bounty of butterflies, which feature day-in, day-out. It should also be made clear that while it appears like a chunk of India which has dropped of the main subcontinent, to frame it, as merely an extension of India, would be a grave injustice, as Sri Lanka feels, looks, and even tastes very different. There are some cultural quirks that make India itself, sometimes challenging to visit for the westerner. -
Nest, Egg, Incubation Behaviour and Parental Care in the Huon Bowerbird Amblyornis Germana
Australian Field Ornithology 2019, 36, 18–23 http://dx.doi.org/10.20938/afo36018023 Nest, egg, incubation behaviour and parental care in the Huon Bowerbird Amblyornis germana Richard H. Donaghey1, 2*, Donna J. Belder3, Tony Baylis4 and Sue Gould5 1Environmental Futures Research Institute, Griffith University, Nathan 4111 QLD, Australia 280 Sawards Road, Myalla TAS 7325, Australia 3Fenner School of Environment and Society, The Australian National University, Canberra ACT 2601, Australia 4628 Utopia Road, Brooweena QLD 4621, Australia 5269 Burraneer Road, Coomba Park NSW 2428, Australia *Corresponding author. Email: [email protected] Abstract. The Huon Bowerbird Amblyornis germana, recently elevated to species status, is endemic to montane forests on the Huon Peninsula, Papua New Guinea. The polygynous males in the Yopno Urawa Som Conservation Area build distinctive maypole bowers. We document for the first time the nest, egg, incubation behaviour, and parental care of this species. Three of the five nests found were built in tree-fern crowns. Nest structure and the single-egg clutch were similar to those of MacGregor’s Bowerbird A. macgregoriae. Only the female Huon Bowerbird incubated. Mean length of incubation sessions was 30.9 minutes and the number of sessions daily was 18. Diurnal incubation constancy over a 12-hour day was 74%, compared with a mean of ~70% in six other members of the bowerbird family. The downy nestling resembled that of MacGregor’s Bowerbird. Vocalisations of a female Huon Bowerbird at a nest with a nestling -
Hybridization & Zoogeographic Patterns in Pheasants
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Paul Johnsgard Collection Papers in the Biological Sciences 1983 Hybridization & Zoogeographic Patterns in Pheasants Paul A. Johnsgard University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/johnsgard Part of the Ornithology Commons Johnsgard, Paul A., "Hybridization & Zoogeographic Patterns in Pheasants" (1983). Paul Johnsgard Collection. 17. https://digitalcommons.unl.edu/johnsgard/17 This Article is brought to you for free and open access by the Papers in the Biological Sciences at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Paul Johnsgard Collection by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. HYBRIDIZATION & ZOOGEOGRAPHIC PATTERNS IN PHEASANTS PAUL A. JOHNSGARD The purpose of this paper is to infonn members of the W.P.A. of an unusual scientific use of the extent and significance of hybridization among pheasants (tribe Phasianini in the proposed classification of Johnsgard~ 1973). This has occasionally occurred naturally, as for example between such locally sympatric species pairs as the kalij (Lophura leucol11elana) and the silver pheasant (L. nycthelnera), but usually occurs "'accidentally" in captive birds, especially in the absence of conspecific mates. Rarely has it been specifically planned for scientific purposes, such as for obtaining genetic, morphological, or biochemical information on hybrid haemoglobins (Brush. 1967), trans ferins (Crozier, 1967), or immunoelectrophoretic comparisons of blood sera (Sato, Ishi and HiraI, 1967). The literature has been summarized by Gray (1958), Delacour (1977), and Rutgers and Norris (1970). Some of these alleged hybrids, especially those not involving other Galliformes, were inadequately doculnented, and in a few cases such as a supposed hybrid between domestic fowl (Gallus gal/us) and the lyrebird (Menura novaehollandiae) can be discounted. -
Bird) Species List
Aves (Bird) Species List Higher Classification1 Kingdom: Animalia, Phyllum: Chordata, Class: Reptilia, Diapsida, Archosauria, Aves Order (O:) and Family (F:) English Name2 Scientific Name3 O: Tinamiformes (Tinamous) F: Tinamidae (Tinamous) Great Tinamou Tinamus major Highland Tinamou Nothocercus bonapartei O: Galliformes (Turkeys, Pheasants & Quail) F: Cracidae Black Guan Chamaepetes unicolor (Chachalacas, Guans & Curassows) Gray-headed Chachalaca Ortalis cinereiceps F: Odontophoridae (New World Quail) Black-breasted Wood-quail Odontophorus leucolaemus Buffy-crowned Wood-Partridge Dendrortyx leucophrys Marbled Wood-Quail Odontophorus gujanensis Spotted Wood-Quail Odontophorus guttatus O: Suliformes (Cormorants) F: Fregatidae (Frigatebirds) Magnificent Frigatebird Fregata magnificens O: Pelecaniformes (Pelicans, Tropicbirds & Allies) F: Ardeidae (Herons, Egrets & Bitterns) Cattle Egret Bubulcus ibis O: Charadriiformes (Sandpipers & Allies) F: Scolopacidae (Sandpipers) Spotted Sandpiper Actitis macularius O: Gruiformes (Cranes & Allies) F: Rallidae (Rails) Gray-Cowled Wood-Rail Aramides cajaneus O: Accipitriformes (Diurnal Birds of Prey) F: Cathartidae (Vultures & Condors) Black Vulture Coragyps atratus Turkey Vulture Cathartes aura F: Pandionidae (Osprey) Osprey Pandion haliaetus F: Accipitridae (Hawks, Eagles & Kites) Barred Hawk Morphnarchus princeps Broad-winged Hawk Buteo platypterus Double-toothed Kite Harpagus bidentatus Gray-headed Kite Leptodon cayanensis Northern Harrier Circus cyaneus Ornate Hawk-Eagle Spizaetus ornatus Red-tailed -
Breeding Biology of the White-Winged Nightjar (Eleothreptus Candicans) in Eastern Paraguay
Revista Brasileira de Ornitologia, 22(2), 219-233 ARTICLE June 2014 Breeding biology of the White-winged Nightjar (Eleothreptus candicans) in eastern Paraguay Robert G. Pople Department of Zoology, University of Cambridge, Downing Street, Cambridge, CB2 3EJ, UK. Email: [email protected] Current address: BirdLife International, Wellbrook Court, Girton Road, Cambridge, CB3 0NA, UK. Received on 03 September 2013. Accepted on 02 October 2013. ABSTRACT: Breeding biology of the White-winged Nightjar (Eleothreptus candicans) in eastern Paraguay. I present the first detailed description of the breeding biology of the White-winged Nightjar (Eleothreptus candicans), based on data collected over three breeding seasons during 1998-2001 at Aguará Ñu, Canindeyú, eastern Paraguay. Male nightjars defended small territories situated on the upper slopes of ridgelines. Each territory contained one or more “display arenas” at which the male performed nuptial display flights. Aggregation indices confirmed that the primary display arenas of males were significantly clustered within the survey area. Within their territories, males apparently selected display arenas on the basis of their structural characteristics: mounds used as arenas were significantly lower and broader than random mounds. Males engaged in display activity from late August to early January. On average, males performed 0.54 ± 0.04 display flights per minute during nocturnal focal watches, but there was considerable intra-male variation in display rate. Following a burst of activity immediately after their arrival at display arenas at dusk, male display rate was best explained by ambient levels of moonlight. Males produced a previously undescribed insect-like “tik tik” call when inactive on their territories. -
An Update of Wallacels Zoogeographic Regions of the World
REPORTS To examine the temporal profile of ChC produc- specification of a distinct, and probably the last, 3. G. A. Ascoli et al., Nat. Rev. Neurosci. 9, 557 (2008). tion and their correlation to laminar deployment, cohort in this lineage—the ChCs. 4. J. Szentágothai, M. A. Arbib, Neurosci. Res. Program Bull. 12, 305 (1974). we injected a single pulse of BrdU into pregnant A recent study demonstrated that progeni- CreER 5. P. Somogyi, Brain Res. 136, 345 (1977). Nkx2.1 ;Ai9 females at successive days be- tors below the ventral wall of the lateral ventricle 6. L. Sussel, O. Marin, S. Kimura, J. L. Rubenstein, tween E15 and P1 to label mitotic progenitors, (i.e., VGZ) of human infants give rise to a medial Development 126, 3359 (1999). each paired with a pulse of tamoxifen at E17 to migratory stream destined to the ventral mPFC 7. S. J. Butt et al., Neuron 59, 722 (2008). + 18 8. H. Taniguchi et al., Neuron 71, 995 (2011). label NKX2.1 cells (Fig. 3A). We first quanti- ( ). Despite species differences in the develop- 9. L. Madisen et al., Nat. Neurosci. 13, 133 (2010). fied the fraction of L2 ChCs (identified by mor- mental timing of corticogenesis, this study and 10. J. Szabadics et al., Science 311, 233 (2006). + phology) in mPFC that were also BrdU+. Although our findings raise the possibility that the NKX2.1 11. A. Woodruff, Q. Xu, S. A. Anderson, R. Yuste, Front. there was ChC production by E15, consistent progenitors in VGZ and their extended neurogenesis Neural Circuits 3, 15 (2009). -
Parallel Evolution of Bower-Building Behavior in Two Groups of Bowerbirds Suggested by Phylogenomics
SUPPLEMENT TO: Parallel Evolution of Bower-Building Behavior in Two Groups of Bowerbirds Suggested by Phylogenomics Per G.P. Ericson 1 *, Martin Irestedt 1, Johan A.A. Nylander 1, Les Christidis 2, Leo Joseph 3, Yanhua Qu 1, 4 * 1 Department of Bioinformatics and Genetics, Swedish Museum of Natural History, PO Box 50007, SE-104 05, Stockholm, Sweden 2 School of Environment, Science and Engineering, Southern Cross University, Coffs Harbour, NSW, Australia, School of BioSciences, University of Melbourne, Parkville, VIC, Australia 3 Australian National Wildlife Collection, CSIRO National Research Collections Australia, Canberra, ACT 2601, Australia 4 Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, China CONTENT 1. MATERIAL AND METHODS (DETAILED DESCRIPTION) 2. FURTHER DETAILS ABOUT SYSTEMATIC RELATIONSHIPS OBSERVED 3. DATA REPOSITORIES 4. SUPPLEMENTARY FIGURES S1-S5 5. SUPPLEMENTARY TABLES S1-S2 1. MATERIAL AND METHODS (DETAILED DESCRIPTION) Taxon Sampling In the study, we include all traditionally recognized bowerbird species as well as representatives for each of the morphologically and genetically distinct populations of the genus Ailuroedus that recently were elevated from status as subspecies to full species (Irestedt et al. 2016). The number of Ailuroedus species thus increased from the traditionally recognized three species (buccoides, crassirostris and melanotis; species epithets used for brevity when possible) to ten (buccoides, stonii, geislerorum, crassirostris, maculosus, melanocephalus, astigmaticus, arfakianus, jobiensis and melanotis). We used cryo-frozen tissue samples for most taxa, but for twelve individuals DNA was extracted from toe pad samples of museum study skins (Table S1 available on Dryad). We base our information on mating system, sexual plumage dimorphism, and building of courts and bowers on Gilliard (1969), Diamond (1986a), Kusmierski et al. -
A Preliminary Risk Assessment of Cane Toads in Kakadu National Park Scientist Report 164, Supervising Scientist, Darwin NT
supervising scientist 164 report A preliminary risk assessment of cane toads in Kakadu National Park RA van Dam, DJ Walden & GW Begg supervising scientist national centre for tropical wetland research This report has been prepared by staff of the Environmental Research Institute of the Supervising Scientist (eriss) as part of our commitment to the National Centre for Tropical Wetland Research Rick A van Dam Environmental Research Institute of the Supervising Scientist, Locked Bag 2, Jabiru NT 0886, Australia (Present address: Sinclair Knight Merz, 100 Christie St, St Leonards NSW 2065, Australia) David J Walden Environmental Research Institute of the Supervising Scientist, GPO Box 461, Darwin NT 0801, Australia George W Begg Environmental Research Institute of the Supervising Scientist, GPO Box 461, Darwin NT 0801, Australia This report should be cited as follows: van Dam RA, Walden DJ & Begg GW 2002 A preliminary risk assessment of cane toads in Kakadu National Park Scientist Report 164, Supervising Scientist, Darwin NT The Supervising Scientist is part of Environment Australia, the environmental program of the Commonwealth Department of Environment and Heritage © Commonwealth of Australia 2002 Supervising Scientist Environment Australia GPO Box 461, Darwin NT 0801 Australia ISSN 1325-1554 ISBN 0 642 24370 0 This work is copyright Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from the Supervising Scientist Requests and inquiries concerning reproduction -
Short Communications
Short Communications The Wilson Journal of Ornithology 118(1):99±101, 2006 Provisioning of Fledgling Conspeci®cs by Males of the Brood-parasitic Cuckoos Chrysococcyx klaas and C. caprius Irby J. Lovette,1,4 Dustin R. Rubenstein,1,2,3 and Wilson Nderitu Watetu3 ABSTRACT.ÐAlthough post-¯edging care by adult Over the past century, there have been nu- males seems unlikely in bird species that are obligate, merous observations of male Chrysococcyx interspeci®c brood parasites, there have been numer- cuckoos feeding conspeci®cs that were ous reports of adult male Chrysococcyx cuckoos ap- parently feeding conspeci®c young. Most researchers thought to be ¯edglings (Moreau 1944, Fried- currently view these observations with skepticism, in mann 1968, Iversen and Hill 1983, Rowan large part because Chrysococcyx and other cuckoo spe- 1983). In a literature review of provisioning cies engage in courtship feeding, and it is possible that behavior in brood parasites, Lorenzana and ®eld observers could mistake adult females receiving Sealy (1998) found 5 records of nestling or food from courting males for ¯edglings, especially giv- en the similar appearances of females and juveniles. ¯edgling provisioning by Klaas's Cuckoo Here, we report an observation of an extended provi- males and 11 such records for Diederik Cuck- sioning bout by an adult male Klaas's Cuckoo (C. oo males; Friedmann (1968) discusses 12 and klaas) feeding a conspeci®c individual with juvenile 15 such records, respectively, including some plumage and behavior, and we summarize our obser- anecdotal reports. There is apparently only vations of similar occurrences in the Diederik Cuckoo one equivalent report of a female Chrysococ- (C. -
A Checklist of the Birds of Goa, India
BAIDYA & BHAGAT: Goa checklist 1 A checklist of the birds of Goa, India Pronoy Baidya & Mandar Bhagat Baidya, P., & Bhagat, M., 2018. A checklist of the birds of Goa, India. Indian BIRDS 14 (1): 1–31. Pronoy Baidya, TB-03, Center for Ecological Sciences, Indian Institute of Science, Bengaluru 560012, Karnataka, India. And, Foundation for Environment Research and Conservation, C/o 407, III-A, Susheela Seawinds, Alto-Vaddem, Vasco-da-Gama 403802, Goa, India. E-mail: [email protected] [Corresponding author] [PB] Mandar Bhagat, ‘Madhumangal’, New Vaddem,Vasco-da-Gama 403802, Goa, India. E-mail: [email protected] [MB] Manuscript received on 15 November 2017. We dedicate this paper to Heinz Lainer, for his commitment to Goa’s Ornithology. Abstract An updated checklist of the birds of Goa, India, is presented below based upon a collation of supporting information from museum specimens, photographs, audio recordings of calls, and sight records with sufficient field notes. Goa has 473 species of birds of which 11 are endemic to the Western Ghats, 19 fall under various categories of the IUCN Red List of Threatened Species, and 48 are listed in Schedule I Part (III) of The Indian Wild Life (Protection) Act, 1972. 451 species have been accepted into the checklist based on specimens in various museums or on photographs, while 22 have been accepted based on sight record. A secondary list of unconfirmed records is also discussed in detail. Introduction that is about 125 km long. The southern portion of these ghats, Goa, India’s smallest state, sandwiched between the Arabian within Goa, juts out towards the Arabian Sea, at Cabo de Rama, Sea in the west and the Western Ghats in the east, is home to and then curves inland. -
Unlocking the Black Box of Feather Louse Diversity: a Molecular Phylogeny of the Hyper-Diverse Genus Brueelia Q ⇑ Sarah E
Molecular Phylogenetics and Evolution 94 (2016) 737–751 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Unlocking the black box of feather louse diversity: A molecular phylogeny of the hyper-diverse genus Brueelia q ⇑ Sarah E. Bush a, , Jason D. Weckstein b,1, Daniel R. Gustafsson a, Julie Allen c, Emily DiBlasi a, Scott M. Shreve c,2, Rachel Boldt c, Heather R. Skeen b,3, Kevin P. Johnson c a Department of Biology, University of Utah, 257 South 1400 East, Salt Lake City, UT 84112, USA b Field Museum of Natural History, Science and Education, Integrative Research Center, 1400 S. Lake Shore Drive, Chicago, IL 60605, USA c Illinois Natural History Survey, University of Illinois, 1816 South Oak Street, Champaign, IL 61820, USA article info abstract Article history: Songbirds host one of the largest, and most poorly understood, groups of lice: the Brueelia-complex. The Received 21 May 2015 Brueelia-complex contains nearly one-tenth of all known louse species (Phthiraptera), and the genus Revised 15 September 2015 Brueelia has over 300 species. To date, revisions have been confounded by extreme morphological Accepted 18 September 2015 variation, convergent evolution, and periodic movement of lice between unrelated hosts. Here we use Available online 9 October 2015 Bayesian inference based on mitochondrial (COI) and nuclear (EF-1a) gene fragments to analyze the phylogenetic relationships among 333 individuals within the Brueelia-complex. We show that the genus Keywords: Brueelia, as it is currently recognized, is paraphyletic. Many well-supported and morphologically unified Brueelia clades within our phylogenetic reconstruction of Brueelia were previously described as genera.