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Handling and Intake of Plastic Debris by Wood Storks at an Urban Site in South-Eastern Brazil: Possible Causes and Consequences
NORTH-WESTERN JOURNAL OF ZOOLOGY 11 (2): 372-374 ©NwjZ, Oradea, Romania, 2015 Article No.: 147601 http://biozoojournals.ro/nwjz/index.html Handling and intake of plastic debris by Wood Storks at an urban site in South-eastern Brazil: possible causes and consequences Ivan SAZIMA1,* and Giulia B. D’ANGELO2 1. Museu de Zoologia, Universidade Estadual de Campinas, 13083-970 Campinas, São Paulo, Brazil. 2. Instituto de Biologia, Universidade Estadual de Campinas, 13083-970 Campinas, São Paulo, Brazil. *Corresponding author, I. Sazima, E-mail: [email protected] Received: 20. September 2014 / Accepted: 12. December 2014 / Available online: 01. November 2015 / Printed: December 2015 Anthropogenic inedible debris increases in the picked pieces of plastic cable were individually identified food chain of seabirds, marine turtles, and by differences on neck feathering and bill colour. cetaceans and becomes a worldwide problem (e.g. Sequenced photographs allowed the timing of the behavioural events for two of these individuals. Denuncio et al. 2011, Avery-Gomm et al. 2013, Throughout the observations, we used the “ad libitum” Schluyter et al. 2013, Donnelly-Greenan et al. 2014, sampling (Altmann 1974), which is adequate to record Provencher et al. 2015), but this material is rarely rare events. reported entering the food chain of inland wildlife (Peris 2003, Booth 2011, Henry et al. 2011). Storks Among small groups of Wood Storks that varied of the genus Ciconia are opportunistic visual from 2 to 8 migrant individuals comprised of up to hunters that prey mostly on fish, frogs, snakes, 2 adults and 6 juveniles, we recorded the small mammals, and a variety of insects (Elliott behaviour of 4 juveniles (subadults sensu Coulton 1992). -
First Record of an Extinct Marabou Stork in the Neogene of South America
First record of an extinct marabou stork in the Neogene of South America JORGE IGNACIO NORIEGA and GERARDO CLADERA Noriega, J.I. and Cladera, G. 2008. First record of an extinct marabou stork in the Neogene of South America. Acta Palaeontologica Polonica 53 (4): 593–600. We describe a new large species of marabou stork, Leptoptilus patagonicus (Ciconiiformes, Ciconiidae, Leptoptilini), from the late Miocene Puerto Madryn Formation, Chubut Province, Argentina. The specimen consists mainly of wing and leg bones, pelvis, sternum, cervical vertebrae, and a few fragments of the skull. We provisionally adopt the traditional system− atic scheme of ciconiid tribes. The specimen is referred to the Leptoptilini on the basis of similarities in morphology and intramembral proportions with the extant genera Ephippiorhynchus, Jabiru,andLeptoptilos. The fossil specimen resembles in overall morphology and size the species of Leptoptilos, but also exhibits several exclusive characters of the sternum, hu− merus, carpometacarpus, tibiotarsus, and pelvis. Additionally, its wing proportions differ from those of any living taxon, providing support to erect a new species. This is the first record of the tribe Leptoptilini in the Tertiary of South America. Key words: Ciconiidae, Leptoptilos, Miocene, Argentina, South America. Jorge I. Noriega [[email protected]], Laboratorio de Paleontología de Vertebrados, CICYTTP−CONICET, Matteri y España, 3105 Diamante, Argentina; Gerardo Cladera [[email protected]], Museo Paleontológico Egidio Feruglio, Avenida Fontana 140, 9100 Trelew, Argentina. Introduction Institutional abbreviations.—BMNH, Natural History Mu− seum, London, UK; CICYTTP, Centro de Investigaciones The stork family (Ciconiidae) is a well−defined group of Científicas y Transferencia de Tecnología a la Producción, waterbirds, traditionally divided into three tribes: the Myc− Diamante, Argentina; CNAR−KB3, collections of locality 3 of teriini, the Ciconiini, and the Leptoptilini (Kahl 1971, 1972, the Kossom Bougoudi area, Centre National d’Appui à la 1979). -
Detailed Species Accounts from The
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. -
Jabiru Mycteria (Jabiru Stork)
UWI The Online Guide to the Animals of Trinidad and Tobago Ecology Jabiru mycteria (Jabiru Stork) Family: Ciconiidae (Storks) Order: Ciconiiformes (Storks, Herons and Ibises) Class: Aves (Birds) Fig. 1. Jabiru stork, Jabiru mycteria. [https://en.wikipedia.org/wiki/Jabiru#/media/File:Jabiru_(Jabiru_mycteria)_2.JPG, downloaded 1 March 2017] TRAITS. Jabiru mycteria is one of the largest flying birds on earth, being the largest in the Americas and one of the three stork species found there. Adult jabiru storks can reach 1.2m tall with a wing span of 2.6m. Their bill is large and black, somewhat upturned, with lengths of up to 30cm (Fig. 1). Males are larger than females, and both sexes can be identified by the band of red skin at the base of the neck. Adult storks possess all-white plumage on the body. The head and neck lacks feathers except for a cluster of grey feathers on the back of the head. The juveniles have white feathers with greyish-brown edges (McKinley, 2006; Borjas, 2004). DISTRIBUTION. Jabiru mycteria is native to South American countries such as Argentina, Brazil, Belize, Colombia, Guyana, Honduras, Nicaragua and Venezuela (Fig. 2). Jabirus can have also been sighted in Mexico, Panama, Trinidad and Tobago, Grenada, United States and Uruguay (IUCN, 2016). UWI The Online Guide to the Animals of Trinidad and Tobago Ecology HABITAT AND ACTIVITY. Jabiru storks are diurnal birds and often feed singly or in pairs but can also be found feeding in large groups (Kahl, 1973). They can be found around coastal lagoons, savannas, marshes and also ponds (Belize Zoo, 2017; Pantanal, 2006). -
Colonial Nesting Waterbirds Fact Sheet
U.S. Fish & Wildlife Service Colonial-Nesting Waterbirds A Glorious and Gregarious Group What Is a Colonial-Nesting Waterbird? species of cormorants, gulls, and terns also Colonial-nesting waterbird is a tongue- occupy freshwater habitats. twister of a collective term used by bird biologists to refer to a large variety of Wading Birds seek their prey in fresh or different species that share two common brackish waters. As the name implies, characteristics: (1) they tend to gather in these birds feed principally by wading or large assemblages, called colonies, during standing still in the water, patiently waiting the nesting season, and (2) they obtain all for fish or other prey to swim within Migratory Bird Management or most of their food (fish and aquatic striking distance. The wading birds invertebrates) from the water. Colonial- include the bitterns, herons, egrets, night- nesting waterbirds can be further divided herons, ibises, spoonbills, and storks. Mission into two major groups depending on where they feed. Should We Be Concerned About the To conserve migratory bird Conservation Status of Colonial-Nesting populations and their habitats Seabirds (also called marine birds, oceanic Waterbirds? birds, or pelagic birds) feed primarily in Yes. While many species of seabirds for future generations, through saltwater. Some seabirds are so appear to have incredibly large careful monitoring and effective marvelously adapted to marine populations, they nevertheless face a management. environments that they spend virtually steady barrage of threats, such as oil their entire lives at sea, returning to land pollution associated with increased tanker only to nest; others (especially the gulls traffic and spills, direct mortality from and terns) are confined to the narrow entanglement and drowning in commercial coastal interface between land and sea, fishing gear, depletion of forage fishes due feeding during the day and loafing and to overexploitation by commercial roosting on land. -
Spread-Wing Postures and Their Possible Functions in the Ciconiidae
THE AUK A QUARTERLY JOURNAL OF ORNITHOLOGY Von. 88 Oc:roBE'a 1971 No. 4 SPREAD-WING POSTURES AND THEIR POSSIBLE FUNCTIONS IN THE CICONIIDAE M. P. KAI-IL IN two recent papers Clark (19'69) and Curry-Lindahl (1970) have reported spread-wingpostures in storks and other birds and discussed someof the functionsthat they may serve. During recent field studies (1959-69) of all 17 speciesof storks, I have had opportunitiesto observespread-wing postures. in a number of speciesand under different environmentalconditions (Table i). The contextsin which thesepostures occur shed somelight on their possible functions. TYPES OF SPREAD-WING POSTURES Varying degreesof wing spreadingare shownby at least 13 species of storksunder different conditions.In somestorks (e.g. Ciconia nigra, Euxenuragaleata, Ephippiorhynchus senegalensis, and ]abiru mycteria) I observedno spread-wingpostures and have foundno referenceto them in the literature. In the White Stork (Ciconia ciconia) I observedonly a wing-droopingposture--with the wings held a short distanceaway from the sidesand the primaries fanned downward--in migrant birds wetted by a heavy rain at NgorongoroCrater, Tanzania. Other species often openedthe wingsonly part way, in a delta-wingposture (Frontis- piece), in which the forearmsare openedbut the primariesremain folded so that their tips crossin front o.f or below the. tail. In some species (e.g. Ibis leucocephalus)this was the most commonly observedspread- wing posture. All those specieslisted in Table i, with the exception of C. ciconia,at times adopted a full-spreadposture (Figures i, 2, 3), similar to those referred to by Clark (1969) and Curry-Lindahl (1970) in severalgroups of water birds. -
Imperiled Coastal Birds of Florida and the State Laws That Protect Them
Reddish Egret Roseate Spoonbill Threatened (S) Threatened (S) Imperiled Coastal The rarest heron in North Using spatulala-shaped Birds of Florida America, Reddish Egrets bills to feel prey in shallow are strictly coastal. They ponds, streams, or coastal and the chase small fish on open waters, Roseate Spoonbills State Laws that flats. They nest in small nest in trees along the numbers on estuary coast and inland. Having Protect Them islands, usually in colonies barely recovered from with other nesting wading hunting eradication, these birds. This mid-sized heron birds now face extirpation is mostly gray with rust- from climate change and colored head, though some sea-level rise. birds are solid white. Wood Stork Florida Sandhill Threatened (F) Florida Statutes and Rules Crane This large wading bird Threatened (S) is the only stork in the 68A-27.003 Designation and management of the state- This crane subspecies is Americas. Breeding areas listed species and coordination with federal government for resident year-round in have shifted from south federally-listed species Florida, and defends a Florida and the Everglades nesting territory that is northward. Wood Storks 68A-19.005 General Regulations relating to state- must have abundant prey adjacent to open upland designated Critical Wildlife Areas foraging habitat. Nesting concentrated in shallow in shallow ponds, adults wetlands in order to feed 68A-4.001 Controls harvest of wildlife only under permitted defend their eggs or chicks their young. Prey items from predators including include -
The History of the Southern Florida Wood Stork Population
Wilson Bull., 98(3), 1986, pp. 368-386 THE HISTORY OF THE SOUTHERN FLORIDA WOOD STORK POPULATION JAMES A. KUSHLAN AND PAULA C. FROHRING ’ AswnAcr.-The largest segment of the North American Wood Stork (Mycteria ameri- cam) population traditionally nested in southern Florida, where its perceived population decrease over the last 50 years resulted in its addition to the Federal endangered species list. Previously published reports placed the southern Florida population at 30,000 to 100,000 storks. A complete search of published and unpublished records of Wood Storks nesting in southern Florida, however, failed to support such a long-term population decrease. We cannot demonstrate that the historical population was any larger than it was in 1967, when there were 9400 pairs. The Corkscrew-Big Cypress nesting group, not that of the Everglades, was historically the most numerically important population segment. The historic nesting location for southernmost Wood Storks was not inland in the Everglades but on Cape Sable, which has been subject to the effects of drainage canals. The population size of several decades ago is irrelevant to current conservation strategy because the southern Florida marshes have been irrevocably altered reducing their ability to support storks. We can document a population decrease of 75% from 1967 to 1981-82 in southern Florida, a time frame coincident with the operation of water management policies in the Everglades. Wood Storks recently have begun abandoning traditional colony sites in Everglades National Park in favor of sites in shallow reservoirs to the north. Drainage of the Big Cypress Swamp and maintenance of seasonally excessive water levels in the Everglades of Everglades National Park account for the storks’ repeated nesting failure and population decrease. -
Factors Affecting Reproductive Success of Wood Storks (Mycteria Americana) in East-Central Georgia
The Auk 112(1):237-243, 1995 FACTORS AFFECTING REPRODUCTIVE SUCCESS OF WOOD STORKS (MYCTERIA AMERICANA) IN EAST-CENTRAL GEORGIA MALCOLM C. COULTER• AND A. LAWRENCEBRYAN, JR. SavannahRiver Ecology Laboratory, Drawer E, Aiken,South Carolina 29802, USA ABS?R•cr.--From1984 through 1989, we examinedthe reproductivesuccess of WoodStorks (Mycteriaamericana) at the Birdsvillecolony in east-centralGeorgia. Average fledging success rangedamong years from 0.33to 2.16fledglings per nest.For neststhat producedfledglings, prey availabilitywas an importantfactor affecting reproductive success. Yearly averageprey densitiesat foragingsites were significantlycorrelated with the averagenumber of fledglings producedfrom successfulnests. Among 243 nestsobserved, all eggsor chickswere lostfrom 104(43%) nests. Five factorswere associatedwith the lossof entire clutchesor broods.During the two driest years, 1985 and 1988, raccoon(Procyon lotor) predation eliminated almost all chicks.Many nestswere abandonedearly in 1989, following periodsof cold weather when the parentsappeared to be under stress.In 1985, the birds desertedthe colony before egg laying when the area experiencedfreezing weather. Following nest abandonmentswithin the colony,paired adultsthat presumablyhad abandonedtheir nestswere involved in nest takeoversthat alsocaused the lossof eggsand chicks.Three stormsduring the studycaused the lossof a few nests.Some losses were due to unknown factors.The importanceof these mortality factorsvaried from year to year. Nest abandonmentsand subsequentaggression seemto be related to cold periodsearly in the season.Raccoon predation seems to be related to drying out of the water under the colony.This suggeststhat the storkshave a window in time when it is bestto breed--afterthe winter and earlyspring cold weather and beforethe water dries under the colony in the summer.Received 4 December1991, accepted 15 November 1992. -
Thailand R I R Lmplemen'rationof Aaicl¢6 of Theconvcntio Lon Biologicaldiversity
r_ BiodiversityConservation in Thailand r i r lmplemen'rationof Aaicl¢6 of theConvcntio_lon BiologicalDiversity Muw_ny of _e_cl reCUr _ eNW_WM#_ I Chapter 1 Biodiversity and Status 1 Species Diversity 1 Genetic Diversity 10 [cosystem Diversity 13 Chapter 2 Activities Prior to the Enactment of the National Strategy on Blodiversity 22 Chapter 3 National Strategy for Implementing the Convention on Biological Diversity 26 Chapter 4 Coordinating Mechanisms for the Implementation of the Convention on Biological Diversity $5 Chapter 5 International Cooperation and Collaboration 61 Chapter 6 Capacity for an Implementation of the Convention on Biological Diversity 70 Annex I National Policies, Measures and Plans on the Conservation and Sustainable Utilization of Biodiversity 1998-2002 80 Annex H Drafted Regulation on the Accress and Transfer of Biological Resources 109 Annex IH Guideline on Biodiversity Data Management (BDM) 114 Annex IV Biodiversity Data Management Action Plan 130 Literature 140 ii Biodiversity Conservation in Thailand: A National Report Preface Regular review of state of biodiversity and its conservation has been recognized by the Convention on Biological Diversity (CBD) as a crucial element in combatting loss of biodiversity. Under Article 6, the Convention's Contracting Parties are obligated to report on implementation of provisions of the Convention including measures formulated and enforced. These reports serve as valuable basic information for operation of the Convention as well as for enhancing cooperation and assistance of the Contracting Parties in achieving conservation and sustainable use of biodiversity. Although Thailand has not yet ratified the Convention, the country has effectively used its provisions as guiding principles for biodiversity conservation and management since the signing of the Convention in 1992. -
Recent Wood Stork Population Trends in the United States
Wilson’ Bull., 91(4), 1979, pp. 512-523 RECENT WOOD STORK POPULATION TRENDS IN THE UNITED STATES JOHN C. OGDEN AND STEPHEN A. NESBITT The population of Wood Storks (Mycteria americana) resident in the United States occurs on the coastal plain of the Gulf of Mexico and the southern Atlantic states. Historically, storks nested in all coastal states from Texas to South Carolina (Bent 1926, Cone and Hall 1970, Dusi and Dusi 1968, Howell 1932, Oberholser 1938, Oberholser and Kincaid 1974, Wayne 1910), although colonies outside Florida formed irregularly and contained few birds. The United States population of storks was not greatly disturbed during the plume-hunting era (Allen 1958), and probably con- tained between 75,000 and 100,000 birds of all age classes during the early twentieth century (Ogden 1978). I ncreased land development and the as- sociated drainage of freshwater wetlands eliminated many nesting and feeding sites, resulting in a severe decline in the total number of storks. Concern for the fate of this species in the United States was first expressed during the late 1950s (Allen 1958, Sprunt and Kahl 1960). A series of aerial surveys was conducted between 1957 and 1960, in an attempt to locate all remaining Wood Stork nesting colonies in the United States. Renewed concern for the status of storks during the early 1970s resulted in a second series of aerial surveys beginning in 1974. These 2 surveys produced the first complete counts of the number of storks nesting in the United States, and revealed that major colonies continued to decline between surveys. -
Painted Storks Mycteria Leucocephala Breeding in Kumarakom Bird Sanctuary, Kerala Shibi Moses
126 Indian BIRDS VOL. 10 NO. 5 (PUBL. 2 NOVEMBER 2015) Painted Storks Mycteria leucocephala breeding in Kumarakom Bird Sanctuary, Kerala Shibi Moses Moses, S., 2015. Painted Storks Mycteria leucocephala breeding in Kumarakom Bird Sanctuary, Kerala. Indian BIRDS 10 (5): 126–127. Shibi Moses, Chackalayil, Kumaranparambil House, Puthuppally PO, Kottayam 686011, Kerala, India. E-mail: [email protected] Manuscript received on 26 August 2014. he Kumarakom Bird Sanctuary (9.62ºN, 76.42ºE) is located and bushy shrubs. The trees were inaccessible either by land or on the banks of the Vembanad Lake, in Kerala. It is 14 km by boat. A watchtower, about 120 m away and 8 m high, was Twest of Kottayam town, the headquarters of the eponymous the only vantage point that could be used for these observations. district. It has Vembanad Lake on its west, the Kumarakom– The branches chosen for the nest sites were bare, despite new Vechoor road on its east, the Kavanar River on the north, and leafy offshoots, and this provided some visibility even from this the KTDC Waterscapes Hotel on the south as its borders. It is distance. Since this opportunity was unique, I decide to monitor a regular nesting and roosting site for eleven species of water the nests on an irregular basis without being stationed at the nest birds like the Great Egret Casmerodius albus, Intermediate site throughout the day. Kumarakom being a mixed heronry, the Egret Mesophoyx intermedia, Little Egret Egretta garzetta, Great birds were tolerant to minor disturbances by visitors and did not Cormorant Phalacrocorax carbo, Indian Cormorant P.