References a Falcated Duck Mareca Falcata X Gadwall M. Strepera Hybrid

Total Page:16

File Type:pdf, Size:1020Kb

References a Falcated Duck Mareca Falcata X Gadwall M. Strepera Hybrid 58 Indian BIRDS VOL. 14 NO. 2 (PUBL. 28 MARCH 2018) I ruled out Western Reef Egret Egretta gularis after referring to Grimmett et al. (2011), as it’s dark morph has a whitish throat, and besides, it looks more like a Little Egret E. garzetta. An earlier record exists, of a grey Cattle Egret, from Dona Paula, Goa, India, on 19 November 1995 (Willoughby 2001). Singh (2013) spotted a melanistic bird at Alinganagar village, in Jharkhand. There seem to be no more cases of colour aberration in this species from India Rajarshi Chakraborty (Mahabal et al. 2016), though these have been noted in other countries (Siegfried 1971; Willoughby 2001; Scheres 2002; Carr 2015). It still has not been established whether a dark morph of Cattle Egret exists, like it does for Little Egret, in spite of the reports of birds, in various shades of grey, from all over the world. 38. Male Falcated Duck X Gadwall hybrid. I retrieved relevant literature from the online ‘Bibliography of South Asian Ornithology’ (Pittie 2017). Table 1. Reports of hybrid Falcated Duck x Gadwall, from India References Site Date Reference Carr, P., 2015. Cattle Egret Bubulcus ibis in the British Indian Ocean Territory: where did Pathshala, Assam April 1917 Robinson (1918) Pinky come from? Birding ASIA 23: 54–55. Harike, Punjab December 2003 Anonymous (2003) Grimmett, R., Inskipp, C., & Inskipp, T., 2011. Birds of the Indian Subcontinent. 2nd ed. London: Oxford University Press & Christopher Helm. Pp. 1–528. Asan Barrage, Uttarakhand January 2008 Anonymous (2008) Mahabal, A., van Grouw, H., Sharma, R. M., & Thakur, S., 2016. How common is Fulbari, West Bengal January 2009 Tharkuta (2009) albinism really? Colour aberrations in Indian birds reviewed. Dutch Birding 38: Maguri Beel, Assam February 2015 Sengupta (2015) 301–309. Maguri Beel, Assam December 2015 Phukan (2015) Pittie, A., 2017. Bibliography of South Asian Ornithology. URL: http://www. Pobitora, Assam February 2016 Das (2016) southasiaornith.in. [Accessed on 20/10/2017.] Scheres, W., 2002. A partly melanistic Cattle Egret Bubulcus ibis. A Rocha Portugal Kaziranga, Assam March 2016 This paper Observatory Report 2002 15. http://www.arocha.org/pt-en/413-DSY/version/ Dighal, Haryana December 2016 Ghosh (2016)* default/part/AttachmentData/data/pt-report-2002.pdf. *Hybrid combination putative Siegfried, W. R., 1971. Plumage and moult of the Cattle Egret. Ostrich 9 (Suppl.): 153–164. Singh, S., 2013. Probable first sighting of dark morph of Eastern Cattle-Egret (sic) Acknowledgements Bubulcus coromandus from Lakhimpur kheri, Uttar Pradesh, India. Journal of the We would like to express our gratitude to Bubul Borah, for providing us transport into Bombay Natural History Society 109 (3): 199 (2012). KNP and helping with the requisite permits, and Dave Appleton, for confirming the Willoughby, P. J., 2001. Melanistic Cattle Egret. British Birds 94: 390–392. identification of the bird. – Leons Mathew Abraham References M. R. Mallik Arcade, 3rd Floor, Near Flyover, Panjabari Road, Six mile, Khanapara, , Guwahati 781022, Assam, India Anonymous. 2003. Falcated Duck Anas falcata (December 2003 mystery bird). E-mail: [email protected] Delhibird-The Northern India Bird Network. Website URL: http://speciesguide. Received on 26 October 2017. delhibird.net/internal/9/falcated_duck.htm. [Accessed on 22 November 2017.] Anonymous. 2008. Falcated Duck Hybrid (presumed): January 2008 Assan Barrage, northern India. Website URL: http://www.harrisbirds.com/Falcated%20Duck%20 A Falcated Duck Mareca falcata x Gadwall M. strepera Hybrid.htm. [Accessed on 22 November 2017.] hybrid at Kaziranga National Park, Assam, India Das, A. K., 2016. Falcated Duck Anas falcata hybrid. Website URL: http://www. A male hybrid between a Falcated Duck Mareca falcata and orientalbirdimages.org/search.php?Bird_ID=216&Bird_Image_ID=115716. Gadwall M. strepera was spotted at 1647 hours, on 25 March [Accessed on 9 January 2018.] 2016 in Kaziranga National Park (henceforth, KNP), Assam, eBird. 2018a. Maps: Gadwall (Marcera strepera). Website URL: http://ebird.org/ebird/ india/map/gadwal. [Accessed on 15 January 2018.] India. The bird was spotted [38] in an open wetland (26.61°N, eBird. 2018b. Maps: Falcated Duck (Marcera falcata). Website URL: http://ebird.org/ 93.34°E) belonging to the central range (Kohora) of KNP. At the ebird/india/map/falduc. [Accessed on 15 January 2018.] time of observation, the bird was feeding in a shallow portion Ghosh, S., 2016. Falcated Duck x Gadwall Anas falcata x Anas strepera—Hybrid. of the wetland, near a mud bank amongst a group of Gadwalls, Website URL: http://www.orientalbirdimages.org/search.php?Bird_ID=216&Bird_ Eurasian Wigeons M. penelope, and a few Indian Spot-billed Image_ID=130675 [Accessed on 9 January 2018.] Ducks Anas poecilorhyncha. Grimmett, R., Inskipp, C., & Inskipp, T., 1998. Birds of the Indian Subcontinent. 1st ed. Both, Falcated Ducks, and Gadwalls are winter migrants to the London: Christopher Helm, A & C Black. Pp. 1–888. north-eastern Indian Subcontinent (Grimmett et al. 2011; eBird Johnson, K. P., & Sorenson, M. D., 1999. Phylogeny and biography of dabbling ducks (genus: Anas): A comparison of molecular and morphological evidence. The Auk 2018a; eBird 2018b) including KNP, where we have recorded 116 (3): 792–805. them in previous seasons. Falcated Duck x Gadwall is one of Phukan, P. J., 2015. Falcated Duck x Gadwall Anas falcata x Anas strepera—Male. the most common waterfowl hybrids found in the wild because Website URL: http://www.orientalbirdimages.org/search.php?Bird_ID=216&Bird_ they are sister species (Johnson & Sorenson 1999). There are Image_ID=113352 [Accessed on 9 January 2018.] a number of instances, since 1918, wherein Falcated Duck x Robinson, H. C., 1918. On two abnormal specimens of ducks in the collection of the Gadwall hybrids, or presumed hybrids, have been reported from Zoological Survey of India. Records of the Indian Museum 15: 47–48. the country, indicating that they are regular in our region too Sengupta, S., 2015. Falcated Duck x Gadwall Anas falcata x Anas strepera—1st winter (Table 1). male. Website URL: http://www.orientalbirdimages.org/search.php?Bird_ ID=216&Bird_Image_ID=102946 [Accessed on 9 January 2018.] Tharkuta, A., 2009. Falcated Duck x Gadwall Anas falcata x Anas strepera—Male. Correspondence 59 Website URL: http://www.orientalbirdimages.org/search.php?Bird_ID=216&Bird_ Image_ID=113351 [Accessed on 9 January 2018.] – Oishik Roy, Tushar Mouli Chakraborti & Rajarshi Chakraborty Oishik Roy, 39/40 Dumdum park, Park Tower, Flat No. 3, Kolkata 700055, West Bengal, India E-mail: [email protected] Tushar Mouli Chakraborti, Department of Geology, Presidency University, 86/1 College Street, Kolkata 700073, West Bengal, India E-mail: [email protected] [Corresponding author] Rajarshi Chakraborty, WWF-India Western Arunachal Landscape Programme, Tezpur, Assam 784001, India. E-mail: [email protected] Received on 23 November 2017. Spot-bellied Eagle-Owl Bubo nipalensis feeding on Indian Flying Fox Pteropus giganteus 40. Spot-bellied Eagle Owl feeding on an Indian flying fox. The Spot-bellied Eagle-Owl Bubo nipalensis is a resident species in Uttarakhand (Rasmussen & Anderton 2012), and occurs in the lower Himalayas upto c. 2100 m asl (Ali & Ripley 1981). a dead Indian flying fox Pteropus giganteus in its talons, and MS has recorded its presence throughout the year in Corbett was feeding on it. The owl was identified as Spot-bellied Eagle Tiger Reserve (MS pers. obsv.). Its habitat has been described Owl, based on such features as: large size, large black-and-white as ‘dense evergreen and moist deciduous forest, usually near horizontal ear-tufts, large yellow beak, fully feathered tarsii, and water, montane wet temperate forest and riparian gallery forest’, prominent spotting on the underparts. and that it ‘hunts also in scrub, bamboo jungle, thin deciduous As per del Hoyo et al. (1999), bats are incidental prey items forest, sometimes edges of clearings’ (del Hoyo et al. 1999). for many owls but, except for one species, owls do not specialise The species is ‘largely nocturnal, spending the day dozing on in preying upon bats. We could not locate any previous records of a densely foliaged bough in the forest, but sometimes on the the Spot-bellied Eagle Owl feeding on bats, and hence this note. move and even hunting during daytime’ (König et al. 1999). It has been recorded taking fair-sized mammals, birds, and reptiles (Resmussen & Anderton 2012). A formidable hunter, it is Acknowledgements recorded taking Kalij Pheasant Lophura leucomelanos, and Red MN wants to thank Naveen Chandra Singh for informing him about the owl, and MS Junglefowl Gallus gallus from their night-time roosts (del Hoyo wants to thank Rakesh Bhatt for bringing the record to his knowledge. To retrieve relevant et al. 1999). Kannan (1995) recorded it preying on the Indian literature we searched the online ‘Bibliography of South Asian Ornithology’ (Pittie 2017). giant squirrel Ratufa indica, and Nandini (2005) found it feeding on an Indian chevrotain Moschiola indica. Its diet is described References consisting of game birds including pheasants, jackals, hare, fawn Ali, S., Ripley, S. D., 1981. Handbook of the birds of India and Pakistan together with of barking deer, lizards, snakes and fish (Ali & Ripley 1981). those of Bangladesh, Nepal, Bhutan and Ceylon. Stone Curlews to Owls. 2nd Garjia Village (29.47°N, 79.15°E; 437m asl) is located on (Hardback) ed. Vol 3 of 10 vols. Delhi (Sponsored by Bombay Natural History the banks of River Kosi, on the eastern boundary of Corbett Society.): Oxford University Press. Pp. i–xvi, 1–327. Tiger Reserve (Uttarakhand, India). The village is surrounded by del Hoyo, J., Elliott, A., & Sargatal, J., (eds.) 1999. Handbook of the birds of the world. mature moist, mixed, and semi-deciduous forests, dominated by Volume 5. Barn-owls to Hummingbirds. 1st ed. Vol. 5 of 17 vols. Barcelona: Lynx sal Shoria robusta on its western side, and a narrow stretch of Edicions.
Recommended publications
  • Disaggregation of Bird Families Listed on Cms Appendix Ii
    Convention on the Conservation of Migratory Species of Wild Animals 2nd Meeting of the Sessional Committee of the CMS Scientific Council (ScC-SC2) Bonn, Germany, 10 – 14 July 2017 UNEP/CMS/ScC-SC2/Inf.3 DISAGGREGATION OF BIRD FAMILIES LISTED ON CMS APPENDIX II (Prepared by the Appointed Councillors for Birds) Summary: The first meeting of the Sessional Committee of the Scientific Council identified the adoption of a new standard reference for avian taxonomy as an opportunity to disaggregate the higher-level taxa listed on Appendix II and to identify those that are considered to be migratory species and that have an unfavourable conservation status. The current paper presents an initial analysis of the higher-level disaggregation using the Handbook of the Birds of the World/BirdLife International Illustrated Checklist of the Birds of the World Volumes 1 and 2 taxonomy, and identifies the challenges in completing the analysis to identify all of the migratory species and the corresponding Range States. The document has been prepared by the COP Appointed Scientific Councilors for Birds. This is a supplementary paper to COP document UNEP/CMS/COP12/Doc.25.3 on Taxonomy and Nomenclature UNEP/CMS/ScC-Sc2/Inf.3 DISAGGREGATION OF BIRD FAMILIES LISTED ON CMS APPENDIX II 1. Through Resolution 11.19, the Conference of Parties adopted as the standard reference for bird taxonomy and nomenclature for Non-Passerine species the Handbook of the Birds of the World/BirdLife International Illustrated Checklist of the Birds of the World, Volume 1: Non-Passerines, by Josep del Hoyo and Nigel J. Collar (2014); 2.
    [Show full text]
  • A 2010 Supplement to Ducks, Geese, and Swans of the World
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Ducks, Geese, and Swans of the World by Paul A. Johnsgard Papers in the Biological Sciences 2010 The World’s Waterfowl in the 21st Century: A 2010 Supplement to Ducks, Geese, and Swans of the World Paul A. Johnsgard University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/biosciducksgeeseswans Part of the Ornithology Commons Johnsgard, Paul A., "The World’s Waterfowl in the 21st Century: A 2010 Supplement to Ducks, Geese, and Swans of the World" (2010). Ducks, Geese, and Swans of the World by Paul A. Johnsgard. 20. https://digitalcommons.unl.edu/biosciducksgeeseswans/20 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 Ducks, Geese, and Swans of the World by Paul A. Johnsgard by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. The World’s Waterfowl in the 21st Century: A 200 Supplement to Ducks, Geese, and Swans of the World Paul A. Johnsgard Pages xvii–xxiii: recent taxonomic changes, I have revised sev- Introduction to the Family Anatidae eral of the range maps to conform with more current information. For these updates I have Since the 978 publication of my Ducks, Geese relied largely on Kear (2005). and Swans of the World hundreds if not thou- Other important waterfowl books published sands of publications on the Anatidae have since 978 and covering the entire waterfowl appeared, making a comprehensive literature family include an identification guide to the supplement and text updating impossible.
    [Show full text]
  • THE FAMILY ANATIDAE 43 Ernst Map
    March 1945 42 THE WILSON BULLETIN Vol. 57, No. 1 Biziura L lob&, Australian Musk Duck Aberrant Species Thalassornis leuconota, African White-backed Duck Heteronetta atricapilla, Black-headed Duck 7. TRIBE MERGANETTINI. TORRENTDUCKS Merganetta armuta, Torrent Duck GENERA RECOGNIZEDBY PETERS AND SYNONYMIZEDIHERE Arctonetta= Som&eria Metopiana= Netta Asarcornis = Cairina Nesochen= Branta Casarca = Tadorna Nesonetta= Anus Chaulelasmus= Anas Nomonyx = Oxyura Chen = Anser Nyroca= Aythya Cheniscus= Nettapus Oidemia = Melanitta Chenopis= Cygnus Phil&e= Anser Cygnopsis= Anser Polysticta= Somateria Dendronessa= Aix Pseudotadorna= Tadorna Eulabeia= Anser Pteronetta= Cairina Lophodytes= Mergus Salvadorina= Anus Mareca= Anas Spatula= Anas Mergellus = Mergus GENERA RECOGNIZEDHERE BUT NOT BY PETERS Amazonetta von Boetticher (for Anus brasiliensis) Lophonetta Riley (for Anus specularioides) COMPARISONOP CHARACTERS Our studies have shown that the waterfowl can be divided into about nine groups that are fairly well defined both morphologically and biologically. In addition, there are a number of species and genera that are either intermediate between the otherwise well- defined tribes (e.g. Coscoroba) or too poorly known for a safe classi- fication (e.g. Anus specularis, Anus leucophrys, Malacorhynchus, Tachyeres) ; others show peculiarities or a combination of characters that prevent them from fitting well into any of the existing groups. Such genera as the Australian Cereopsis, Anseranas, Stictonetta, and Chenonetta could either be made the sole representatives of so many separate tribes or each could be included in the tribe with which it shares the greatest number of similarities. For the sake of con- venience we have adopted the latter course, but without forgetting that these genera are not typical representatives of the tribes with which we associate them.
    [Show full text]
  • Viruses in Migratory Birds, China, 2013–2014
    Article DOI: http://dx.doi.org/10.3201/eid2206.151754 Novel Avian Influenza A(H5N8) Viruses in Migratory Birds, China, 2013–2014 Technical Appendix Materials and Methods Wild Bird Surveillance and Sampling Wild birds were captured and sampled with the permission and supervision of Shanghai Wild Life Conservation and Management Office. Swabs (1 oropharyngeal and 1 cloacal of each bird) were taken and transported in viral transport medium to the laboratory at 4°C for downstream molecular diagnosis within 6 hours. Virus Detection Viral RNA was extracted from viral transport medium by using MagMAXTM Pathogen RNA/DNA Kit (Applied Biosystems, Foster City, CA, USA) on a Magmax-96 Express (Applied Biosystems) according to the manufacturer’s instructions. Real time reverse transcription-PCR was performed with matrix gene–specific probed primers to detect the presence of avian influenza viruses according to the protocol of the Chinese Center for Disease Control and Prevention (1). The results were further confirmed by sequencing the PCR products. Subtype Identification and Gene Sequencing RNA of viral-positive samples were reverse-transcribed by PrimeScript II Reverse Transcriptase Kit (TaKaRa, Biotechnology [Dalian] Co., Ltd, Dalian, China) according to the kit protocol. PCR amplifications were performed for subtyping of hemagglutinin (HA) and neuraminidase, and gene segments were amplified by using the previously published primers (2– Page 1 of 5 4) and primers designed in this study (on request). PCR products were gel-purified by using the QIAquick gel extraction kit (QIAGEN, Valencia, CA, USA) and were sequenced with the BigDye terminator kit (Applied Biosystems) on an ABI 3730 (Applied Biosystems).
    [Show full text]
  • European Red List of Birds 2015
    Mareca strepera (Gadwall) European Red List of Birds Supplementary Material The European Union (EU27) Red List assessments were based principally on the official data reported by EU Member States to the European Commission under Article 12 of the Birds Directive in 2013-14. For the European Red List assessments, similar data were sourced from BirdLife Partners and other collaborating experts in other European countries and territories. For more information, see BirdLife International (2015). Contents Reported national population sizes and trends p. 2 Trend maps of reported national population data p. 6 Sources of reported national population data p. 9 Species factsheet bibliography p. 17 Recommended citation BirdLife International (2015) European Red List of Birds. Luxembourg: Office for Official Publications of the European Communities. Further information http://www.birdlife.org/datazone/info/euroredlist http://www.birdlife.org/europe-and-central-asia/european-red-list-birds-0 http://www.iucnredlist.org/initiatives/europe http://ec.europa.eu/environment/nature/conservation/species/redlist/ Data requests and feedback To request access to these data in electronic format, provide new information, correct any errors or provide feedback, please email [email protected]. THE IUCN RED LIST OF THREATENED SPECIES™ BirdLife International (2015) European Red List of Birds Mareca strepera (Gadwall) Table 1. Reported national breeding population size and trends in Europe1. Country (or Population estimate Short-term population trend4 Long-term population trend4 Subspecific population (where relevant) 2 territory) Size (pairs)3 Europe (%) Year(s) Quality Direction5 Magnitude (%)6 Year(s) Quality Direction5 Magnitude (%)6 Year(s) Quality Albania 0-5 <1 2002-2012 poor ? ? Armenia 250-400 <1 2002-2012 medium ? ? Austria 250-350 <1 2001-2012 good 0 0 2001-2012 medium + 50-100 1980-2012 medium M.
    [Show full text]
  • Beijing & Yunnan, China, with OBC
    Beijing & Yunnan, China, with OBC. An at-a-glance list of 436 species of birds & eight species of mammals recorded. By Jesper Hornskov ® ***this draft 22 Aug 2010*** ALL RIGHTS RESERVED Please note that the following list is best considered a work in progress. It should not be quoted without consulting the author . Based mostly on my own field notes, this brief write-up covers the birds & mammals noted by C Clifford (until 27 March), C Dietzen, P Drake-Brockman, R East, W Grossi, E Patterson, P Post, W v d Schot, N Zalinge & myself during the 15 March – 3 April 2010 OBC Fundraiser trip to Beijing’s Botanical Garden, and Lijiang, Gaoligongshan, Tengchong, the Yingjiang area & Ruili. We recorded 436 species of birds and eight species of mammals on the 'main tour', very similar totals to those of a private tour in 2008 & the 2009 OBC Fundraiser. An additional 24 species were noted when eight of us covered Beijing's Wild Duck Lake on 4 th - to make it easier for future participants to decide if it might be worth their while to extend their visit by a day or two these are mentioned in the list but are not included in the total species tally - and quite a few more, notably Long-billed Plover Charadrius placidus , and Tristram’s Emberiza tristrami & Yellow-browed Buntings E. chrysophrys , were found during 'non-scheduled' excursions before and after the trip. Beijing's winter returned with a vengeance in the run-up to the trip, with thick snow in the mountains preventing access to the Ibisbill site on 14 March.
    [Show full text]
  • Handbook of Waterfowl Behavior: Tribe Anatini (Surface-Feeding Ducks)
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Handbook of Waterfowl Behavior, by Paul Johnsgard Papers in the Biological Sciences January 1965 Handbook of Waterfowl Behavior: Tribe Anatini (Surface-feeding Ducks) Paul A. Johnsgard University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/bioscihandwaterfowl Part of the Ornithology Commons Johnsgard, Paul A., "Handbook of Waterfowl Behavior: Tribe Anatini (Surface-feeding Ducks)" (1965). Handbook of Waterfowl Behavior, by Paul Johnsgard. 16. https://digitalcommons.unl.edu/bioscihandwaterfowl/16 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 Handbook of Waterfowl Behavior, by Paul Johnsgard by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Subfamily Anatinae 125 Aix. During extreme excitement the male will often roll his head on his back, or even bathe. I have not observed Preening-behind-the- wing, but W. von de Wall (pers. comm.) has observed a male per- form it toward a female. Finally, Wing-flapping appears to be used as a display by males, and it is especially conspicuous because each sequence of it is ended by a rapid stretching of both wings over the back in a posture that makes visible the white axillary feathers, which contrast sharply with the black underwing surface. Copulatory behavior. Precopulatory behavior consists of the male swimming up to the female, his neck stretched and his crest de- pressed, and making occasional Bill-dipping movements. He then suddenly begins to perform more vigorous Head-dipping movements, and the female, if receptive, performs similar Bill-dipping or Head- dipping movements.
    [Show full text]
  • Ducks, Geese, and Swans of the World by Paul A
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Ducks, Geese, and Swans of the World by Paul A. Johnsgard Papers in the Biological Sciences 2010 Ducks, Geese, and Swans of the World: Index Paul A. Johnsgard University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/biosciducksgeeseswans Part of the Ornithology Commons Johnsgard, Paul A., "Ducks, Geese, and Swans of the World: Index" (2010). Ducks, Geese, and Swans of the World by Paul A. Johnsgard. 19. https://digitalcommons.unl.edu/biosciducksgeeseswans/19 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 Ducks, Geese, and Swans of the World by Paul A. Johnsgard by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Index The following index is limited to the species of Anatidae; species of other bird families are not indexed, nor are subspecies included. However, vernacular names applied to certain subspecies that sometimes are considered full species are included, as are some generic names that are not utilized in this book but which are still sometimes applied to par­ ticular species or species groups. Complete indexing is limited to the entries that correspond to the vernacular names utilized in this book; in these cases the primary species account is indicated in italics. Other vernacular or scientific names are indexed to the section of the principal account only. Abyssinian blue-winged goose. See atratus, Cygnus, 31 Bernier teal. See Madagascan teal blue-winged goose atricapilla, Heteronetta, 365 bewickii, Cygnus, 44 acuta, Anas, 233 aucklandica, Anas, 214 Bewick swan, 38, 43, 44-47; PI.
    [Show full text]
  • (2007): Birds of the Aleutian Islands, Alaska Please
    Bold* = Breeding Sp Su Fa Wi Bold* = Breeding Sp Su Fa Wi OSPREYS FINCHES Osprey Ca Ca Ac Brambling I Ca Ca EAGLES and HAWKS Hawfinch I Ca Northern Harrier I I I Common Rosefinch Ca Eurasian Sparrowhawk Ac (Ac) Pine Grosbeak Ca Bald Eagle* C C C C Asian Rosy-Finch Ac Rough-legged Hawk Ac Ca Ca Gray-crowned Rosy-Finch* C C C C OWLS (griseonucha) Snowy Owl I Ca I I Gray-crowned Rosy-Finch (littoralis) Ac Short-eared Owl* R R R U Oriental Greenfinch Ca FALCONS Common Redpoll I Ca I I Eurasian Kestrel Ac Ac Hoary Redpoll Ca Ac Ca Ca Merlin Ca I Red Crossbill Ac Gyrfalcon* R R R R White-winged Crossbill Ac Peregrine Falcon* (pealei) U U C U Pine Siskin I Ac I SHRIKES LONGSPURS and SNOW BUNTINGS Northern Shrike Ca Ca Ca Lapland Longspur* Ac-C C C-Ac Ac CROWS and JAYS Snow Bunting* C C C C Common Raven* C C C C McKay's Bunting Ca Ac LARKS EMBERIZIDS Sky Lark Ca Ac Rustic Bunting Ca Ca SWALLOWS American Tree Sparrow Ac Tree Swallow Ca Ca Ac Savannah Sparrow Ca Ca Ca Bank Swallow Ac Ca Ca Song Sparrow* C C C C Cliff Swallow Ca Golden-crowned Sparrow Ac Ac Barn Swallow Ca Dark-eyed Junco Ac WRENS BLACKBIRDS Pacific Wren* C C C U Rusty Blackbird Ac LEAF WARBLERS WOOD-WARBLERS Bold* = Breeding Sp Su Fa Wi Wood Warbler Ac Yellow Warbler Ac Dusky Warbler Ac Blackpoll Warbler Ac DUCKS, GEESE and SWANS Kamchatka Leaf Warbler Ac Yellow-rumped Warbler Ac Emperor Goose C-I Ca I-C C OLD WORLD FLYCATCHERS "HYPOTHETICAL" species needing more documentation Snow Goose Ac Ac Gray-streaked Flycatcher Ca American Golden-plover (Ac) Greater White-fronted Goose I
    [Show full text]
  • A Molecular Phylogeny of Anseriformes Based on Mitochondrial DNA Analysis
    MOLECULAR PHYLOGENETICS AND EVOLUTION Molecular Phylogenetics and Evolution 23 (2002) 339–356 www.academicpress.com A molecular phylogeny of anseriformes based on mitochondrial DNA analysis Carole Donne-Goussee,a Vincent Laudet,b and Catherine Haanni€ a,* a CNRS UMR 5534, Centre de Genetique Moleculaire et Cellulaire, Universite Claude Bernard Lyon 1, 16 rue Raphael Dubois, Ba^t. Mendel, 69622 Villeurbanne Cedex, France b CNRS UMR 5665, Laboratoire de Biologie Moleculaire et Cellulaire, Ecole Normale Superieure de Lyon, 45 Allee d’Italie, 69364 Lyon Cedex 07, France Received 5 June 2001; received in revised form 4 December 2001 Abstract To study the phylogenetic relationships among Anseriformes, sequences for the complete mitochondrial control region (CR) were determined from 45 waterfowl representing 24 genera, i.e., half of the existing genera. To confirm the results based on CR analysis we also analyzed representative species based on two mitochondrial protein-coding genes, cytochrome b (cytb) and NADH dehydrogenase subunit 2 (ND2). These data allowed us to construct a robust phylogeny of the Anseriformes and to compare it with existing phylogenies based on morphological or molecular data. Chauna and Dendrocygna were identified as early offshoots of the Anseriformes. All the remaining taxa fell into two clades that correspond to the two subfamilies Anatinae and Anserinae. Within Anserinae Branta and Anser cluster together, whereas Coscoroba, Cygnus, and Cereopsis form a relatively weak clade with Cygnus diverging first. Five clades are clearly recognizable among Anatinae: (i) the Anatini with Anas and Lophonetta; (ii) the Aythyini with Aythya and Netta; (iii) the Cairinini with Cairina and Aix; (iv) the Mergini with Mergus, Bucephala, Melanitta, Callonetta, So- materia, and Clangula, and (v) the Tadornini with Tadorna, Chloephaga, and Alopochen.
    [Show full text]
  • Alpha Codes for 2168 Bird Species (And 113 Non-Species Taxa) in Accordance with the 62Nd AOU Supplement (2021), Sorted Taxonomically
    Four-letter (English Name) and Six-letter (Scientific Name) Alpha Codes for 2168 Bird Species (and 113 Non-Species Taxa) in accordance with the 62nd AOU Supplement (2021), sorted taxonomically Prepared by Peter Pyle and David F. DeSante The Institute for Bird Populations www.birdpop.org ENGLISH NAME 4-LETTER CODE SCIENTIFIC NAME 6-LETTER CODE Highland Tinamou HITI Nothocercus bonapartei NOTBON Great Tinamou GRTI Tinamus major TINMAJ Little Tinamou LITI Crypturellus soui CRYSOU Thicket Tinamou THTI Crypturellus cinnamomeus CRYCIN Slaty-breasted Tinamou SBTI Crypturellus boucardi CRYBOU Choco Tinamou CHTI Crypturellus kerriae CRYKER White-faced Whistling-Duck WFWD Dendrocygna viduata DENVID Black-bellied Whistling-Duck BBWD Dendrocygna autumnalis DENAUT West Indian Whistling-Duck WIWD Dendrocygna arborea DENARB Fulvous Whistling-Duck FUWD Dendrocygna bicolor DENBIC Emperor Goose EMGO Anser canagicus ANSCAN Snow Goose SNGO Anser caerulescens ANSCAE + Lesser Snow Goose White-morph LSGW Anser caerulescens caerulescens ANSCCA + Lesser Snow Goose Intermediate-morph LSGI Anser caerulescens caerulescens ANSCCA + Lesser Snow Goose Blue-morph LSGB Anser caerulescens caerulescens ANSCCA + Greater Snow Goose White-morph GSGW Anser caerulescens atlantica ANSCAT + Greater Snow Goose Intermediate-morph GSGI Anser caerulescens atlantica ANSCAT + Greater Snow Goose Blue-morph GSGB Anser caerulescens atlantica ANSCAT + Snow X Ross's Goose Hybrid SRGH Anser caerulescens x rossii ANSCAR + Snow/Ross's Goose SRGO Anser caerulescens/rossii ANSCRO Ross's Goose
    [Show full text]
  • Eligible Species for the Junior Duck Stamp Competition
    Eligible Species for the Junior Duck Stamp Competition Your entry should feature a live portrayal featuring at least one of the species below. Mute swans, loons, grebes, coots and other such waterbirds are not permitted species. For the contest, you may do ones not found in Maine Species found in Maine ● Snow Goose, including blue phase (Anser caerulescens) ● Greater White-fronted Goose (Anser albifrons) ● Brant (Branta bernicla) ● Canada Goose (Branta canadensis) ● Wood Duck (Aix sponsa) ● Blue-winged Teal (Spatula discors) ● Northern Shoveler (Spatula clypeata) ● Gadwall (Mareca strepera) ● American Wigeon (Mareca americana) ● Mallard (Anas platyrhynchos) ● American Black Duck (Anas rubripes) ● Northern Pintail (Anas acuta) ● Green-winged Teal (Anas crecca) ● Ring-necked Duck (Aythya collaris) ● Greater Scaup (Aytha marila) ● Lesser Scaup (Aythya affinis) ● King Eider (Somateria spectabilis) ● Common Eider (Somateria mollissima) ● HarleQuin Duck (Histrionicus histrionicus) Threatened Species ME ● Surf Scoter (Melanitta perspicillata) ● White-winged Scoter (Melanitta fusca) ● Black Scoter (Melanitta americana) ● Long-tailed Duck (Clangula hyemalis) ● Bufflehead (Bucephala albeola) ● Common Goldeneye (Bucephala clangula) ● Barrow's Goldeneye (Bucephala islandica) Threatened Species ME ● Hooded Merganser (Lophodytes cucullatus) ● Common Merganser (Mergus merganser) ● Red-breasted Merganser (Mergus serrator) ● Ruddy Duck (Oxyura jamaicensis) Species not found in Maine (usually) but still eligible ● Black-bellied Whistling-Duck (Dendrocygna
    [Show full text]