Australian Crane (Grus Rubicundus)
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Quantifying Crop Damage by Grey Crowned Crane Balearica
QUANTIFYING CROP DAMAGE BY GREY CROWNED CRANE BALEARICA REGULORUM REGULORUM AND EVALUATING CHANGES IN CRANE DISTRIBUTION IN THE NORTH EASTERN CAPE, SOUTH AFRICA. By MARK HARRY VAN NIEKERK Department of the Zoology and Entomology, Rhodes University Submitted in partial fulfilment of the requirements for the Degree of MASTER OF SCIENCE December 2010 Supervisor: Prof. Adrian Craig i TABLE OF CONTENTS List of tables…………………………………………………………………………iv List of figures ………………………………………………………………………...v Abstract………………………………………………………………………………vii I. INTRODUCTION .......................................................................................... 1 Species account......................................................................................... 3 Habits and diet ........................................................................................... 5 Use of agricultural lands by cranes ............................................................ 6 Crop damage by cranes ............................................................................. 7 Evaluating changes in distribution and abundance of Grey Crowned Crane………………………………………………………..9 Objectives of the study………………………………………………………...12 II. STUDY AREA…………………………………………………………………...13 Locality .................................................................................................... 13 Climate ..................................................................................................... 15 Geology and soils ................................................................................... -
Birds of Bharatpur – Check List
BIRDS OF BHARATPUR – CHECK LIST Family PHASIANIDAE: Pheasants, Partridges, Quail Check List BLACK FRANCOLIN GREY FRANCOLIN COMMON QUAIL RAIN QUAIL JUNGLE BUSH QUAIL YELLOW-LEGGED BUTTON QUAIL BARRED BUTTON QUAIL PAINTED SPURFOWL INDIAN PEAFOWL Family ANATIDAE: Ducks, Geese, Swans GREATER WHITE-FRONTED GOOSE GREYLAG GOOSE BAR-HEADED GOOSE LWSSER WHISTLING-DUCK RUDDY SHELDUCK COMMON SHELDUCK COMB DUCK COTTON PYGMY GOOSE MARBLED DUCK GADWALL FALCATED DUCK EURASIAN WIGEON MALLARD SPOT-BILLED DUCK COMMON TEAL GARGANEY NORTHERN PINTAIL NORTHERN SHOVELER RED-CRESTED POCHARD COMMON POCHARD FERRUGINOUS POCHARD TUFTED DUCK BAIKAL TEAL GREATER SCAUP BAER’S POCHARD Family PICIDAE: Woodpeckers EURASIAN WRYNECK BROWN-CAPPED PYGMY WOODPECKER YELLOW-CROWNED WOODPECKER BLACK-RUMPED FLAMBACK Family CAPITONIDAE: Barbets BROWN-HEADED BARBET COPPERSMITH BARBET Family UPUPIDAE: Hoopoes COMMON HOOPOE Family BUCEROTIDAE: Hornbills INDAIN GREY HORNBILL Family CORACIIDAE: Rollers or Blue Jays EUROPEAN ROLLER INDIAN ROLLER Family ALCEDINIDAE: Kingfisher COMMON KINGFISHER STORK-BILLED KINGFISHER WHITE-THROATED KINGFISHER BLACK-CAPPED KINGFISHER PIED KINGFISHER Family MEROPIDAE: Bee-eaters GREEN BEE-EATER BLUE-CHEEKED BEE-EATER BLUE-TAILED BEE-EATER Family CUCULIDAE: Cuckoos, Crow-pheasants PIED CUCKOO CHESTNUT-WINGED CUCKOO COMMON HAWK CUCKOO INDIAN CUCKOO EURASIAN CUCKOO GREY-BELLIED CUCKOO PLAINTIVE CUCKOO DRONGO CUCKOO ASIAN KOEL SIRKEER MALKOHA GREATER COUCAL LESSER COUCAL Family PSITTACIDAS: Parrots ROSE-RINGED PARAKEET PLUM-HEADED PARKEET Family APODIDAE: -
A Taxono1vhc Revision of the Genus Faradaya F. Muell
J. Adelaide Bot. Gard 10(2): 165-177 (1987) A TAXONO1VHC REVISION OF THE GENUS FARADAYA F. MUELL. (VERBENACEAE)* IN AUSTRALIA Ahmad Abid Munir State Herbarium, Botanic Gardens, North Terrace, Adelaide, South Australia 5000 Abstract A taxonomic revision of Faradaya in Australia is presented. The following two species are recognised: F. albertisii and E splendida. F. albertisii is confirmed from Australia. A wide range of material has been examined from Malesia and Oceania. The affinities and distribution are considered for the genus and each species. A key to the species is provided and a detailed description of each species is supplemented by an illustration. Taxonomic History of the Genus The genus Faradaya was described by F. Mueller (1865) with one species, E splendida, the type of which came from Queensland. Originally it was placed in the Bignoniaceae, but soon after its publication, Seemann (1865) referred the genus to the "Natural Order Verbenaceae, closely related to Clerodendrum and Oxera". The family Verbenaceae has been accepted for the genus by all subsequent botanists. Earlier, one Faradaya collection from Tonga and another from Fiji were respectively described by Seemann (1862) and Asa Gray (1862) as new species of Clerodendrum. In view of their difference from other Clerodendrum taxa, Asa Gray (1862) formed for them a new section of the genus namely Clerodendrum sect. Tetrathyranthus A. Gray. Subsequently, Seemann (1865) recognised both types of the section Tetrathyranthus as Faradaya species and thus reduced this section to synonymy under Faradaya. Bentham (1870, 1876) divided the family Verbenaceae into different tribes, with Faradaya in the tribe Viticeae subtribe Oxereae. -
Grey Crowned Cranes
grey crowned cranes www.olpejetaconservancy.org GREY CROWNED CRANES are one of 15 species of crane. Their name comes from the impressive spray of stiff golden feathers that form a crown around their heads. Crowned cranes inhabit a range of wetlands and prefer short to medium height open grasslands for foraging. THREATS TO CROWNED CRANES The grey crowned crane is categorised as Endangered in the IUCN Red List. Populations have decreased significantly, estimated at around 80% since 1985. The main threats to cranes are habitat loss, illegal trade, and poisoning. They are considered status symbols among the wealthy. Birds are captured and eggs removed and illegally sold in large numbers. As human settlements expand, cranes are closer to farmland which they forage millet and potatoes. Large numbers are killed each year in Kenya as retaliation or to prevent crop damage. CROWNED CRANES AT OL PEJETA Ol Pejeta sits in Laikipia County which has the 5th largest crowned crane population in Kenya. In 2019, nearly 160 crown cranes were counted at the conservancy. Unfortunately, the population has been observed to be OL PEJETA on a decline. 160 POPULATION The cranes utilise marshy areas across the conservancy. Flocks of 10- 30 individuals are often observed on neighbouring wheat farms. They migrate into Ol Pejeta in search of food and are seen in large numbers during the rainy season. DID YOU KNOW? CROWNED CRANES TRACKS Crowned cranes mate for life. They dance together and preen each others necks to help strengthen their bond. www.olpejetaconservancy.org [email protected] . -
157 Common Crane Put Your Logo Here
Javier Blasco -Zumeta & Gerd -Michael Heinze Sponsor is needed. Write your name here 157 Common Crane Put your logo here SEXING Plumage of both sexes alike. Size and colour on base of bill can be useful in extreme birds: male with wing longer than 585 mm, base of bill bright red; female with wing shorter than 560 mm, base of bill duller red. MOULT Complete postbreeding moult but not all years since flight feathers are all changed every 2nd to perhaps even every 4th years. Partial postjuve- nile moult involving only many body feathers; usually finished by October. PHENOLOGY I II III IV V VI VII VIII IX X XI XII COMMON CRANE (Grus grus ) STATUS IN ARAGON IDENTIFICATION - On passage and winter visitor, with presen- 108 140 cm. Adult with slate grey plumage; ce mainly in Gallocanta and some places of throat, nape and sides of face black; white sides of head and neck; red crown; black primaries; the Ebro Basin. long secondaries forming a bushy tail; long legs. Juvenile with brown plumage; chestnut head; shorter secondaries. SIMILAR SPECIES This species is unmistakable AGEING Since the species doesn’t breed in Aragon, only 3 types of age can be recognized: 1st year autumn/2nd year spring with a patch of black tinged red skin on crown; rufous head and upper neck; with a pale patch behind the eye; ash grey body, usually with feathers on upperparts edged brown. 2nd year autumn/3rd year spring like adult , but crown not as bare; some retained old brown feathers on scapulars; wing coverts, tertials and underparts; usually with juvenile primaries and secondaries, which are narrower and pointed than in adult . -
Sustainable Conservation and Management of Indian Sarus Crane (Grus Antigone Antigone) in and Around Alwara Lake of District Kaushambi (U.P.), India
ISSN:150 2394-1391 Indian Journal of Biology Volume 5 Number 2, July - December 2018 Original Article DOI: http://dx.doi.org/10.21088/ijb.2394.1391.5218.7 Sustainable Conservation and Management of Indian Sarus crane (Grus antigone antigone) in and around Alwara Lake of District Kaushambi (U.P.), India Ashok Kumar Verma1, Shri Prakash2 Abstract The Indian Sarus crane, Grus antigone antigone is the only resident breeding crane of Indian subcontinent that has been declared as ‘State Bird’ by the Government of Uttar Pradesh. This is one of the most graceful, monogamous, non-migratory and tallest flying bird of the world that pair for lifelong and famous for marital fidelity. Population of this graceful bird now come in vulnerable situation due to the shrinking of wetlands at an alarming speed in the country. Present survey is aimed to study the population of sarus crane in the year 2017 in and around the Alwara Lake of district Kaushambi (Uttar Pradesh) India and their comparison to sarus crane population recorded from 2012 to 2016 in the same study area. This comparison reflects an increasing population trend of the said bird in the area studied. It has been observed that the prevailing ecological conditions of the lake, crane friendly behaviour of the local residents and awareness efforts of the authors have positive correlation in the sustainable conservation and increasing population trends of this vulnerable bird. Keywords: Alwara Lake; Conservation; Population Census; Sarus Crane; Increasing Trend. Introduction Author’s Affiliation: 1Head, Department of Zoology, Govt. P.G. College, Saidabad, Prayagraj, Uttar Pradesh 221508, India. -
Recommended Band Size List Page 1
Jun 00 Australian Bird and Bat Banding Scheme - Recommended Band Size List Page 1 Australian Bird and Bat Banding Scheme Recommended Band Size List - Birds of Australia and its Territories Number 24 - May 2000 This list contains all extant bird species which have been recorded for Australia and its Territories, including Antarctica, Norfolk Island, Christmas Island and Cocos and Keeling Islands, with their respective RAOU numbers and band sizes as recommended by the Australian Bird and Bat Banding Scheme. The list is in two parts: Part 1 is in taxonomic order, based on information in "The Taxonomy and Species of Birds of Australia and its Territories" (1994) by Leslie Christidis and Walter E. Boles, RAOU Monograph 2, RAOU, Melbourne, for non-passerines; and “The Directory of Australian Birds: Passerines” (1999) by R. Schodde and I.J. Mason, CSIRO Publishing, Collingwood, for passerines. Part 2 is in alphabetic order of common names. The lists include sub-species where these are listed on the Census of Australian Vertebrate Species (CAVS version 8.1, 1994). CHOOSING THE CORRECT BAND Selecting the appropriate band to use combines several factors, including the species to be banded, variability within the species, growth characteristics of the species, and band design. The following list recommends band sizes and metals based on reports from banders, compiled over the life of the ABBBS. For most species, the recommended sizes have been used on substantial numbers of birds. For some species, relatively few individuals have been banded and the size is listed with a question mark. In still other species, too few birds have been banded to justify a size recommendation and none is made. -
A Grammar of Komnzo
A grammar of Komnzo Christian Döhler language Studies in Diversity Linguistics 22 science press Studies in Diversity Linguistics Editor: Martin Haspelmath In this series: 1. Handschuh, Corinna. A typology of marked-S languages. 2. Rießler, Michael. Adjective attribution. 3. Klamer, Marian (ed.). The Alor-Pantar languages: History and typology. 4. Berghäll, Liisa. A grammar of Mauwake (Papua New Guinea). 5. Wilbur, Joshua. A grammar of Pite Saami. 6. Dahl, Östen. Grammaticalization in the North: Noun phrase morphosyntax in Scandinavian vernaculars. 7. Schackow, Diana. A grammar of Yakkha. 8. Liljegren, Henrik. A grammar of Palula. 9. Shimelman, Aviva. A grammar of Yauyos Quechua. 10. Rudin, Catherine & Bryan James Gordon (eds.). Advances in the study of Siouan languages and linguistics. 11. Kluge, Angela. A grammar of Papuan Malay. 12. Kieviet, Paulus. A grammar of Rapa Nui. 13. Michaud, Alexis. Tone in Yongning Na: Lexical tones and morphotonology. 14. Enfield, N. J. (ed.). Dependencies in language: On the causal ontology of linguistic systems. 15. Gutman, Ariel. Attributive constructions in North-Eastern Neo-Aramaic. 16. Bisang, Walter & Andrej Malchukov (eds.). Unity and diversity in grammaticalization scenarios. 17. Stenzel, Kristine & Bruna Franchetto (eds.). On this and other worlds: Voices from Amazonia. 18. Paggio, Patrizia and Albert Gatt (eds.). The languages of Malta. 19. Seržant, Ilja A. & Alena Witzlack-Makarevich (eds.). Diachrony of differential argument marking. 20. Hölzl, Andreas. A typology of questions in Northeast Asia and beyond: An ecological perspective. 21. Riesberg, Sonja, Asako Shiohara & Atsuko Utsumi (eds.). Perspectives on information structure in Austronesian languages. 22. Döhler, Christian. A grammar of Komnzo. ISSN: 2363-5568 A grammar of Komnzo Christian Döhler language science press Döhler, Christian. -
An Assessment of Threats to Anatidae in Iran
Bird Conservation International (2015) 25 :242 –257 . © BirdLife International, 2014 doi:10.1017/S0959270914000264 An assessment of threats to Anatidae in Iran ELHAM NOURANI , MOHAMMAD KABOLI and BEN COLLEN Summary The network of wetland systems in Iran provides valuable staging and wintering areas for waterbirds in the African-Western Eurasian flyways. The West Siberian/Caspian/Nile popula- tions of Anatidae (ducks, geese and swans) regularly overwinter and stop over in Iran, and are considered an economically and culturally important group of birds in the country. Conservation of such migratory birds requires the identification of key threat factors impacting them throughout the flyway. Since documented data on the status and threats facing Anatidae in Iran are very scarce, in this paper, we attempted to determine the general population trends for the 26 Anatidae species in Iran, using annual waterbird census data, and to identify and score the most important threat factors affecting each species, by consulting the top ornithologists and pro- fessional birdwatchers in the country by means of a survey. Our results indicate that the most prevalent threats affecting all 26 species are dam construction, water management practices, and hunting. Our results provide the necessary material for Red List assessment of these species at the national level, an important tool for conservation priority setting within Iran and in the flyway. Introduction Waterbirds have long been the subject of many international conservation agreements. The Convention on Wetlands (Ramsar, Iran, 1971) and the Agreement on the Conservation of African- Eurasian Migratory Waterbirds (AEWA, 1999), among others, urge countries to work together to save migratory waterbirds through the flyway concept. -
Brolga Grus Rubicunda
Action StatementNo 119 Brolga Grus rubicunda Indexof Action Stetements *xDescription and Distribution * LifeHistorv and Ecoloqv *ConservationStatus *Decline andThreats *ManaqeqentAgtion *xReferences **Compilers Brolga, Grus rubicunda (illustrationby SusannaHaffenden) Descriptionand Distribution The BrolgaGrus rubicunda (Perry) is a large,long-necked 'lr cranestanding to 1.8metres in height.They have long, darklegs and their plumage is predominanflylight grey in colour.The average wing span of an adultis 1.7-2.4 "k-: metres.The adultmale weighs 4.7-8.7 kilograms and the female3.7-7 .3 kilograms(Marchant and Higgins 1993). Adultshave a conspicuousorange-red head which contrastswith the barecrown of greenish-greyskin and the darkerpendulous dewlap. The billis dark,long and straightand relativelylarge compared to the head.The iris ..;;, is yellowto reddish-orange.lmmatures (up to 10 months of age)have a grey,fully feathered head and the irisis darkbrown. Juveniles (11to22 months)gradually lose the headfeathering and attainthe red headcolouring. A fulldescription can be foundin Marchantand Higgins illrtr{but}on In Vlcteria (1ee3) +b€fere 1970 I sincg ,1570 {s+urce: S#as of tf,efonsr $,!#dlds.FlftE lgSSl The Brolgais distributedacross New Guinea, northern andsouth-eastern Australia (Blakers et al. 1g84, Marchantand Higgins1993). The populationsin Victoria andSouth Australia may now be isolatedfrom the northernpopulations as thereappear to be onlyscattered birdsin NewSouth Wales. In Victoria,birds are currentlyfound in the south-west,the NorthernPlains and adjacentparts of the MurrayRiver (Emison et al.1987).The specieswas formerlymore widely distributed and common,being recorded from the Melbournearea, Gippsland and North-easternVictoria (White 1e83). Life historyand ecology The Brolgais omnivorousand utilisesa diverserange of fooditems on a seasonalbasis. -
Wintering Behavior of a Siberian Crane Grus Leucogeranus in Niigata, Japan, with Special Regard to Food, Foraging and Vocal Habits
Ornithol Sci 17: 187 – 194 (2018) ORIGINAL ARTICLE Wintering behavior of a Siberian Crane Grus leucogeranus in Niigata, Japan, with special regard to food, foraging and vocal habits Akira CHIBA#,* 1-13-11 Terao-Higashi, Niigata 950–2054, Japan ORNITHOLOGICAL Abstract An immature Siberian Crane Grus leucogeranus straggled to Niigata, Japan, in late autumn 2016 and remained over winter in an area of rice fields. In this SCIENCE paper the bird’s diet and foraging behavior during winter 2016/2017 are described. © The Ornithological Society During daytime, the crane foraged alone, mostly on post-harvest rice fields where of Japan 2018 it fed almost exclusively on Water Chestnut Eleocharis kuroguwai tubers. Other foods, such as rice grains, earthworms, grasshoppers and fishes, though eaten, were negligible in the bird’s diet. The density of water chestnut tubers in the foraging area was estimated to be 3.1±3.0/m2 and the biomass 2.0±2.1 g/m2. The crane’s foraging behavior generally included removing any superficial covering material, digging into and removing the soil, exploring the food in the beak and then consuming it with or without rinsing it in groundwater. During foraging, the frequency of food intake varied from 4.8±2.0/10 min to 41.3±9.5/10 min. These results indicate the great significance of water chestnuts in the diet of the Siberian Crane in winter, although further study is necessary for generalization. Key words Diet, Foraging, Grus leucogeranus, Rice field, Water chestnuts The Siberian Crane Grus leucogeranus is regarded al. 2017). Such information has contributed to our as a critically endangered species by the International understanding of the current situation of the species Union for Conservation of Nature, with a global pop- in the wild, and has promoted further investigation ulation of 3,500 to 4,000 individuals (Bird Life Inter- and conservation. -
First Arizona Record of Common Crane
Arizona Birds - Journal of Arizona Field Ornithologists Volume 2020 FIRST ARIZONA RECORD OF COMMON CRANE JOE CROUSE,1125 W. SHULLENBARGER DR., FLAGSTAFF, AZ 86005 The first record of a Common Crane (Grus grus), a Eurasian species, in Arizona was reported in May 2017 at Mormon Lake in Coconino County. It remained at this lake through September 2017. In 2019 a Common Crane was reported 11 May through 31 August at Mormon Lake. The 2017 record has been reviewed and accepted by the Arizona Bird Committee (Rosenberg et al. 2019), and the 2019 bird has been accepted as the same individual. The Common Crane is a widespread crane found in Europe, Asia, the Middle East, and North Africa. Breeding occurs across northern Europe and northern Asia, from Norway on the west to Siberia on the east. Nonbreeding populations are found as far west as Morocco and to southeastern China. A resident population exists in Turkey (NatureServe and IUCN 2017, Figure 1). Preferred habitat for both breeding and nonbreeding birds is small ponds or lakes, wet meadows, and other wetland areas (Cramp and Simmons 1980). Figure 1. Common Crane Distribution Cramp and Simmons (1980) stated that the Common Crane range in western Europe has had a “marked” decrease since the Middle Ages. They attributed this to the draining of nesting areas. Since 1950 improved habitat protections, recolonization in previously inhabited areas, and designation as a protected species have resulted in a dramatic increase in the overall population (Prange 2005). Although its range has decreased, it continues to be extensive enough, along with the increase in its already large population, to give it the status of a species of “Least Concern” (BirdLife International 2016, NatureServe and IUCN 2019).