Threatened Birds of India: Need for Immediate Conservation Action
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Introduction
Threatened Birds of Asia: The BirdLife International Red Data Book Editors N. J. COLLAR (Editor-in-chief), A. V. ANDREEV, S. CHAN, M. J. CROSBY, S. SUBRAMANYA and J. A. TOBIAS Maps by RUDYANTO and M. J. CROSBY Principal compilers and data contributors ■ BANGLADESH P. Thompson ■ BHUTAN R. Pradhan; C. Inskipp, T. Inskipp ■ CAMBODIA Sun Hean; C. M. Poole ■ CHINA ■ MAINLAND CHINA Zheng Guangmei; Ding Changqing, Gao Wei, Gao Yuren, Li Fulai, Liu Naifa, Ma Zhijun, the late Tan Yaokuang, Wang Qishan, Xu Weishu, Yang Lan, Yu Zhiwei, Zhang Zhengwang. ■ HONG KONG Hong Kong Bird Watching Society (BirdLife Affiliate); H. F. Cheung; F. N. Y. Lock, C. K. W. Ma, Y. T. Yu. ■ TAIWAN Wild Bird Federation of Taiwan (BirdLife Partner); L. Liu Severinghaus; Chang Chin-lung, Chiang Ming-liang, Fang Woei-horng, Ho Yi-hsian, Hwang Kwang-yin, Lin Wei-yuan, Lin Wen-horn, Lo Hung-ren, Sha Chian-chung, Yau Cheng-teh. ■ INDIA Bombay Natural History Society (BirdLife Partner Designate) and Sálim Ali Centre for Ornithology and Natural History; L. Vijayan and V. S. Vijayan; S. Balachandran, R. Bhargava, P. C. Bhattacharjee, S. Bhupathy, A. Chaudhury, P. Gole, S. A. Hussain, R. Kaul, U. Lachungpa, R. Naroji, S. Pandey, A. Pittie, V. Prakash, A. Rahmani, P. Saikia, R. Sankaran, P. Singh, R. Sugathan, Zafar-ul Islam ■ INDONESIA BirdLife International Indonesia Country Programme; Ria Saryanthi; D. Agista, S. van Balen, Y. Cahyadin, R. F. A. Grimmett, F. R. Lambert, M. Poulsen, Rudyanto, I. Setiawan, C. Trainor ■ JAPAN Wild Bird Society of Japan (BirdLife Partner); Y. Fujimaki; Y. Kanai, H. -
Breeding Seabirds at Dassen Island, South Africa: Chances of Surviving Great White Pelican Predation
Vol. 9: 125–131, 2010 ENDANGERED SPECIES RESEARCH Published online January 11 doi: 10.3354/esr00243 Endang Species Res OPENPEN ACCESSCCESS Breeding seabirds at Dassen Island, South Africa: chances of surviving great white pelican predation Martin M. Mwema1, 2,*, Marta de Ponte Machado1, 2, Peter G. Ryan1 1Percy Fitzpatrick Institute, DST/NRF Centre of Excellence, University of Cape Town, Rondebosch 7701, South Africa 2Animal Demography Unit, Department of Zoology, University of Cape Town, Rondebosch 7701, South Africa Present address: Box 1019, 00100, GPO, Nairobi, Kenya ABSTRACT: Seabird predation by great white pelicans Pelecanus onocrotalus is an unusual phenom- enon that has become increasingly frequent in the Western Cape, South Africa. We report the scale of pelican predation and its impact on the breeding success of 5 seabird species monitored at Dassen Island in 2006. Pelican predation was observed on chicks of kelp gulls Larus dominicanus, crowned cormorants Phalacrocorax coronatus and Cape cormorants Phalacrocorax capensis. No predation on eggs was seen. Breeding success for 4 of the 5 species studied was low, with the white-breasted cor- morants Phalacrocorax lucidus having the highest breeding success (0.56 fledglings per nest). Cape and bank cormorants Phalacrocorax neglectus did not fledge any chicks, while crowned cormorants had a breeding success of 0.08 fledglings per nest. Kelp gulls had a hatching success of 46%, but only a few chicks fledged, giving a breeding success of 0.06 fledglings per nest. Pelican predation poses a threat to at least 3 of the 5 seabirds studied, all of which are endemic to southern Africa. Three spe- cies are globally Endangered or Near Threatened, and pelican predation places additional pressure on these species. -
Building Bridges for Migratory Waterbird Conservation in the Central Asian Flyway
46 Indian Birds Vol. 1 No. 2 (March-April 2005) SATHIYASELVAM, P. 2004. Nidification and site middle of the woods. 44 (5): 79. February): Backcover. fidelity of the Black-crowned Night SINGH, Baljit. 2004. Comments on the cover THAKUR, Sanjay, and Aparna Watve. 2004. Heron, (Nycticorax nycticorax). 44 (4) photo. 44 (1) (January-February): Report of Lesser Kestrel (Falco (July-August): 63. Backcover. naumanni Fleischer) flock near SAXENA, Rajiv, and Gaurav Parihar. 2004. SINGHA, Hilloljyoti, Amarjit Narayan Dev, Thoseghar, Satara Dt. Maharashtra. 44 (4) Pesticides killing Demoiselle Cranes. 44 Rimpul Hazarika, Kaustoov Gopal (July-August): 60. (3) (May-June): 48. (With one b&w Goswami, and Banita Roy. 2004. Waterfowl TULJAPURKAR, Vijay. 2004. Birds in my photo.). census in Dheer Beel, Assam. 44 (3) garden. 44 (5): 75-78. SHARMA, Arunayan. 2004. Red-necked Grebe (May-June): 45. UTTANGI, J. C. 2004. Non-stop call of the (Podiceps griseigena) in West Bengal, a SIVAKUMAR, S., and Vibhu Prakash. 2004. Coppersmith, (Megalaima correction. 44 (1) (January-February): 15. Miscellaneous breeding information of haemacephala) observed lasting for —. 2004. Asian Koels are the first caller birds Collared Falconet Microhierax seven minutes in Dharwad urbans. 44 (2) of the day. 44 (2) (March-April): 29-30. caerulescens. 44 (4) (July-August): 57-58. (March-April): 29. (With two text-figs.). SRIDHAR, S. 2004. A note from the publisher: —. 2004. Robbing of eggs by female Koel, SHIVAPRAKASH, A. 2004. Nature trai in Anshi E. Hanumantha Rao no more. 44 (2) from the nest of Red-whiskered Bulbul forest area, North Kanara District, (March-April): 19. -
CMS/CAF/Inf.4.13 1 Central Asian Flyway Action Plan for Waterbirds and Their Habitat Country Report
CMS/CAF/Inf.4.13 Central Asian Flyway Action Plan for Waterbirds and their Habitat Country Report - INDIA A. Introduction India situated north of the equator covering an area of about 3,287,263 km2 is one of the largest country in the Asian region. With 10 distinctly different bio geographical zones and many different habitat types, the country is known amongst the top 12 mega biodiversity countries. India is known to support 1225 species of bird species, out of these 257 species are water birds. India remains in the core central region of the Central Asian Flyway (CAF) and holds some crucial important wintering population of water bird species. India is also a key breeding area for many other water birds such as Pygmy cormorant and Ruddy-shelduck, globally threatened water birds such as Dalmatian Pelican, Lesser White-fronted Goose, Siberian crane, oriental white stork, greater adjutant stork, white winged wood duck etc. Being located in the core of the CAF, and several important migration routes the country covers a large intra-continental territory between Arctic and Indian Ocean. Being aware of the importance of the wetlands within the geographic boundary of the India for migrating avifauna, India has developed a wetland conservation programme. India currently has 19 RAMSAR sites. India has identified more than 300 sites which has the potential to be consider as the RAMSAR sites. However, being the second most populus nation in the world with agricultural economy, wetlands are one of the most used habitat with water bird and human interface. Much of the Indian landmass also being dependent to the normal monsoonal rainfall for precipitation is also subjected to extremes of drought and flood making the wetlands vulnerable to drastic ecological changes. -
Movements of a Nomadic Waterfowl, Grey Teal Anas Gracilis, Across Inland Australia – Results from Satellite Telemetry Spanning Fifteen Months
Movements of a nomadic waterfowl, Grey Teal Anas gracilis, across inland Australia – results from satellite telemetry spanning fifteen months D.A. Roshier1,*, N.I. Klomp1 & M. Asmus1 Roshier D.A., Klomp N.I. & Asmus M. 2006. Movements of a nomadic waterfowl, Grey Teal Anas gracilis, across inland Australia – results from satellite telemetry spanning fifteen months. Ardea 94(3): 461–475. We used lightweight satellite transmitters to follow the movements of 17 Grey Teal Anas gracilis between September 2003 and November 2004 in two contrasting landscapes, the agricultural districts of southern Australia and the desert landscapes of the interior. Tagged birds moved large dis- tances (up to 343 km) between occupied sites in a short period (hours), remained in the vicinity of those sites for extended periods (months), ven- tured up to 453 km from their point of release and travelled more than 2000 km in one year. We describe patterns of movement in a nomadic waterfowl for 15 months from September 2003, a period of severe drought. Based on the current analysis there appears to be no remarkable difference in the observed patterns of movement of those released in the agricultural landscapes and those released in the desert. As in waterfowl elsewhere, movements appear to occur in response to changes in local food abundance that threaten survival or the imperative to move in order to breed successfully. In Grey Teal, the proximate cues for movement transcend the local landscape and some birds are responding to temporary cues hundreds of kilometres distant. This is in contrast to the universal seasonal cues associated with migration systems else- where. -
Phylogeny Biogeography, and Taxonomy of Australasian
The Auk 117(1):154-163, 2000 PHYLOGENY, BIOGEOGRAPHY, AND TAXONOMY OF AUSTRALASIAN TEALS MARTYN KENNEDY 1 AND HAMISH G. SPENCER Departmentof Zoology,University of Otago,P.O. Box 56, Dunedin,New Zealand ABSTRACT.--Thetaxonomy of the Australasianteals has been particularly unstable. Aus- tralasianGrey Teal (Anasgracilis) and ChestnutTeal (A. castanea)are widely viewed asspe- cificallydistinct, but the taxonomyof theNew Zealandteals remains unsettled. Because con- servationstatus is affectedby taxonomicrank, it is importantto resolvethe statusof the rare subantarcticteals. To estimatephylogenetic relationships of teals,we sequencedthree mi- tochondrialDNA genes(12S, and ATPase6 and 8). The resultantphylogeny unequivocally groupsthe ChestnutTeal with the GreyTeal, rather than with the New Zealandteals as has traditionally been held (Fleming 1953). A greater level of sequencedivergence occurred within the New Zealandteals than betweenthe Grey and Chestnutteals. This diversity,to- getherwith morphologicaland behavioraldifferences, implies that the New Zealandteals shouldbe accordedspecific status as A. aucklandica,A. nesiotis,and A. chlorotis.Although it is most likely that the teal that colonizedthe AucklandIslands and CampbellIslands orig- inated in New Zealand, our data do not allow us to determine whether the ancestors of the CampbellIsland Teal came from mainlandNew Zealandor the AucklandIslands. This un- certaintyarises because, as our data show,the colonizationevents were separatedby a short period of time. Received25 November1998, accepted 16 June1999. F•VE EXTANT TEALS inhabit the Australasian 1990).The brown-plumagedteals (i.e. all teals region and provide an interesting example of exceptthe Grey Teal)all existin allopatry.The speciationin insularSouthern Hemisphere wa- Auckland Island Teal (A. aucklandica)and terfowl (see Livezey 1990). Grey Teal (Anas CampbellIsland Teal (A. nesiotis)occur only on gracilis),which are small and drab, are wide- their respectivesubantarctic island groups (see spreadthroughout Australia. -
Conservation Status of New Zealand Birds, 2008
Notornis, 2008, Vol. 55: 117-135 117 0029-4470 © The Ornithological Society of New Zealand, Inc. Conservation status of New Zealand birds, 2008 Colin M. Miskelly* Wellington Conservancy, Department of Conservation, P.O. Box 5086, Wellington 6145, New Zealand [email protected] JOHN E. DOWDING DM Consultants, P.O. Box 36274, Merivale, Christchurch 8146, New Zealand GRAEME P. ELLIOTT Research & Development Group, Department of Conservation, Private Bag 5, Nelson 7042, New Zealand RODNEY A. HITCHMOUGH RALPH G. POWLESLAND HUGH A. ROBERTSON Research & Development Group, Department of Conservation, P.O. Box 10420, Wellington 6143, New Zealand PAUL M. SAGAR National Institute of Water & Atmospheric Research, P.O. Box 8602, Christchurch 8440, New Zealand R. PAUL SCOFIELD Canterbury Museum, Rolleston Ave, Christchurch 8001, New Zealand GRAEME A. TAYLOR Research & Development Group, Department of Conservation, P.O. Box 10420, Wellington 6143, New Zealand Abstract An appraisal of the conservation status of the post-1800 New Zealand avifauna is presented. The list comprises 428 taxa in the following categories: ‘Extinct’ 20, ‘Threatened’ 77 (comprising 24 ‘Nationally Critical’, 15 ‘Nationally Endangered’, 38 ‘Nationally Vulnerable’), ‘At Risk’ 93 (comprising 18 ‘Declining’, 10 ‘Recovering’, 17 ‘Relict’, 48 ‘Naturally Uncommon’), ‘Not Threatened’ (native and resident) 36, ‘Coloniser’ 8, ‘Migrant’ 27, ‘Vagrant’ 130, and ‘Introduced and Naturalised’ 36. One species was assessed as ‘Data Deficient’. The list uses the New Zealand Threat Classification System, which provides greater resolution of naturally uncommon taxa typical of insular environments than the IUCN threat ranking system. New Zealand taxa are here ranked at subspecies level, and in some cases population level, when populations are judged to be potentially taxonomically distinct on the basis of genetic data or morphological observations. -
India's National Action Plan for Conservation of Migratory Birds and Their Habitats Along Central Asian Flyway
India’s National Action Plan for Conservation of Migratory Birds and their Habitats along Central Asian Flyway (2018-2023) CAF National Action Plan 2018 -India Drafting Committee: The Draft India National Action Plan for Conservation of Migratory Birds in Central Asian Flyway was prepared by the following committee constituted by the Ministry of Environment, Forest and Climate Change: Dr. Soumitra Dasgupta, IG F (WL), Ministry of Environment, Forest and Climate Change (Chairman) Dr. Nita Shah, Bombay Natural History Society (Member) Dr. Ritesh Kumar, Wetlands International South Asia (Member) Dr. Suresh Kumar, Wildlife Institute of India (Member) Mr. C. Sasikumar, Wildlife Division, Ministry of Environment, Forest and Climate Change The Committee met at Keoladeo National Park, Bharatpur on December 12-13, 2017 and at the office of IG F (WL) on March 15, 2018 and April 12, 2018 to review drafts. The final draft National Action Plan was submitted by the Committee on April 14, 2018. Final review of the draft was done in the office of IG (WL) on May 8, 2018. [1] CAF National Action Plan 2018 -India Contents Abbreviations .................................................................................................................................... 3 Preamble ........................................................................................................................................... 4 Goal and Objectives ......................................................................................................................... -
Nepal's Birds 2010
Bird Conservation Nepal (BCN) Established in 1982, Bird Conservation BCN is a membership-based organisation Nepal (BCN) is the leading organisation in with a founding President, patrons, life Nepal, focusing on the conservation of birds, members, friends of BCN and active supporters. their habitats and sites. It seeks to promote Our membership provides strength to the interest in birds among the general public, society and is drawn from people of all walks OF THE STATE encourage research on birds, and identify of life from students, professionals, and major threats to birds’ continued survival. As a conservationists. Our members act collectively result, BCN is the foremost scientific authority to set the organisation’s strategic agenda. providing accurate information on birds and their habitats throughout Nepal. We provide We are committed to showing the value of birds scientific data and expertise on birds for the and their special relationship with people. As Government of Nepal through the Department such, we strongly advocate the need for peoples’ of National Parks and Wildlife Conservation participation as future stewards to attain long- Birds Nepal’s (DNPWC) and work closely in birds and term conservation goals. biodiversity conservation throughout the country. As the Nepalese Partner of BirdLife International, a network of more than 110 organisations around the world, BCN also works on a worldwide agenda to conserve the world’s birds and their habitats. 2010 Indicators for our changing world Indicators THE STATE OF Nepal’s Birds -
Botulism Is a Paralytic Disease Caused by Ingestion of a Toxin Produced by the Bacterium Clostridium Botulinum
Fact sheet Botulism is a paralytic disease caused by ingestion of a toxin produced by the bacterium Clostridium botulinum. Avian botulism can occur in any bird species, but is most frequently seen in ducks, geese, swans, ibis, egrets and pelicans. It occurs worldwide and is commonly reported in wild birds in Australia. The majority of birds that develop botulism will die if not treated. Toxin production by C. botulinum only occurs under specific environmental conditions. Most outbreaks of botulism occur in the summer and autumn and often occur repeatedly in the same environment. Large numbers of birds can die during outbreaks and this can contribute to local and regional population declines. Order: Clostridiales Family: Clostridiaceae Genus: Clostridium Clostridium botulinum is a Gram-positive, rod-shaped bacterium that produces environmentally resistant spores when faced with unfavourable conditions. It grows in environments where there is little or no oxygen. Clostridium botulinum isolates can produce any one of seven distinct types of neurotoxins (A-G). Most produce only one neurotoxin, but some isolates will produce multiple toxins. Clostridium botulinum isolates are also categorized into groups I-IV by their ability to use protein substrates for energy. Toxin production is generally group specific and Group III strains are associated with animal disease. Ingestion of the toxin causes the paralytic disease known as botulism. Waterfowl mortalities due to botulism are usually caused by type C toxin (or type C/D mosaic), although type E has caused sporadic mortalities among fish-eating birds (such as gulls) mainly around the Great Lakes in North America (Rocke and Bollinger 2007; Le Maréchal et al. -
Hybridisation in the Last Remaining Individuals Of
Records of the Canterbury Museum, 2017 Vol. 31: 159–165 © Canterbury Museum 2017 159 Hybridisation in the last remaining individuals of the extinct Fiordland population of Brown Teal (Anas chlorotis) Theresa L Cole1,2 and Jamie R Wood1 1Landcare Research, PO Box 69040, Lincoln 7640, New Zealand Email: [email protected] 2Department of Zoology, University of Otago, PO Box 56, Dunedin 9054, New Zealand The New Zealand endemic Brown Teal (Anas chlorotis Gray, 1845) was once widespread on the three main islands of New Zealand, some offshore islands and the Chatham Islands. Hunting and drainage of wetlands during the early years of European colonisation, however, resulted in a severely reduced range for the species and by 1990, the last remaining wild populations were on Great Barrier Island, and in eastern Northland and Fiordland. However, by 2007, the Fiordland population of Brown Teal was assumed extinct. The potential role of hybridisation with Mallard (Anas platyrhynchos Linnaeus, 1758) and Grey Duck (Anas superciliosa Gmelin, 1789) in the decline of the Fiordland population of Brown Teal has previously been recognised, though specimen details and tissue voucher samples associated with the DNA sequences were not retained. Here, we provide new mitochondrial DNA sequences from four specimens of Fiordland Brown Teal registered in the collections of Canterbury Museum. The results provide evidence for hybridisation with Mallard/ Grey Duck in all four individuals, and support previous suggestions that hybridisation could have played a role in the decline of the Fiordland Brown Teal population. Keywords: Conservation, genetics, Mallard, museum, voucher specimens Introduction The New Zealand endemic Brown Teal Anas( Teal were on Great Barrier Island, and in eastern chlorotis Gray, 1845), or pāteke, was formerly Northland and Fiordland (Gemmell and Flint widespread on the three main islands of New 2000). -
Lead in Victorian Wetlands Study Preliminary Investigation
Lead in Victorian wetlands s tudy P reliminary investigation Publication 1681 December 2017 Lake Martin, May 2017 Lake Martin, May 2017 1 Lead in Victorian wetlands study 2017 About this report This report has been prepared by Environment Protection Authority Victoria (EPA); published December 2017. EPA publication 1681 For further information, please contact EPA on 1300 372 842 (1300 EPA VIC) or [email protected] Translation service Translation: 131 450 2 Lead in Victorian wetlands study 2017 Contents List of figures and tables ................................................................................................................................................... 4 Glossary of terms .............................................................................................................................................................. 5 Executive summary ........................................................................................................................................................... 6 Project background ........................................................................................................................................................... 7 Objectives ......................................................................................................................................................................... 7 Methods ...........................................................................................................................................................................