Sacred Ibis (Threskiornis Aethiopicus)1
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The Phylogenetic Position of Ambiortus: Comparison with Other Mesozoic Birds from Asia1 J
ISSN 00310301, Paleontological Journal, 2013, Vol. 47, No. 11, pp. 1270–1281. © Pleiades Publishing, Ltd., 2013. The Phylogenetic Position of Ambiortus: Comparison with Other Mesozoic Birds from Asia1 J. K. O’Connora and N. V. Zelenkovb aKey Laboratory of Evolution and Systematics, Institute of Vertebrate Paleontology and Paleoanthropology, 142 Xizhimenwai Dajie, Beijing China 10044 bBorissiak Paleontological Institute, Russian Academy of Sciences, Profsoyuznaya ul. 123, Moscow, 117997 Russia email: [email protected], [email protected] Received August 6, 2012 Abstract—Since the last description of the ornithurine bird Ambiortus dementjevi from Mongolia, a wealth of Early Cretaceous birds have been discovered in China. Here we provide a detailed comparison of the anatomy of Ambiortus relative to other known Early Cretaceous ornithuromorphs from the Chinese Jehol Group and Xiagou Formation. We include new information on Ambiortus from a previously undescribed slab preserving part of the sternum. Ambiortus is superficially similar to Gansus yumenensis from the Aptian Xiagou Forma tion but shares more morphological features with Yixianornis grabaui (Ornithuromorpha: Songlingorni thidae) from the Jiufotang Formation of the Jehol Group. In general, the mosaic pattern of character distri bution among early ornithuromorph taxa does not reveal obvious relationships between taxa. Ambiortus was placed in a large phylogenetic analysis of Mesozoic birds, which confirms morphological observations and places Ambiortus in a polytomy with Yixianornis and Gansus. Keywords: Ornithuromorpha, Ambiortus, osteology, phylogeny, Early Cretaceous, Mongolia DOI: 10.1134/S0031030113110063 1 INTRODUCTION and articulated partial skeleton, preserving several cervi cal and thoracic vertebrae, and parts of the left thoracic Ambiortus dementjevi Kurochkin, 1982 was one of girdle and wing (specimen PIN, nos. -
156 Glossy Ibis
Text and images extracted from Marchant, S. & Higgins, P.J. (co-ordinating editors) 1990. Handbook of Australian, New Zealand & Antarctic Birds. Volume 1, Ratites to ducks; Part B, Australian pelican to ducks. Melbourne, Oxford University Press. Pages 953, 1071-1 078; plate 78. Reproduced with the permission of Bird life Australia and Jeff Davies. 953 Order CICONIIFORMES Medium-sized to huge, long-legged wading birds with well developed hallux or hind toe, and large bill. Variations in shape of bill used for recognition of sub-families. Despite long legs, walk rather than run and escape by flying. Five families of which three (Ardeidae, Ciconiidae, Threskiornithidae) represented in our region; others - Balaenicipitidae (Shoe-billed Stork) and Scopidae (Hammerhead) - monotypic and exclusively Ethiopian. Re lated to Phoenicopteriformes, which sometimes considered as belonging to same order, and, more distantly, to Anseriformes. Behavioural similarities suggest affinities also to Pelecaniformes (van Tets 1965; Meyerriecks 1966), but close relationship not supported by studies of egg-white proteins (Sibley & Ahlquist 1972). Suggested also, mainly on osteological and other anatomical characters, that Ardeidae should be placed in separate order from Ciconiidae and that Cathartidae (New World vultures) should be placed in same order as latter (Ligon 1967). REFERENCES Ligon, J.D. 1967. Occas. Pap. Mus. Zool. Univ. Mich. 651. Sibley, C. G., & J.E. Ahlquist. 1972. Bull. Peabody Mus. nat. Meyerriecks, A.J. 1966. Auk 83: 683-4. Hist. 39. van Tets, G.F. 1965. AOU orn. Monogr. 2. 1071 Family PLATALEIDAE ibises, spoonbills Medium-sized to large wading and terrestial birds. About 30 species in about 15 genera, divided into two sub families: ibises (Threskiornithinae) and spoonbills (Plataleinae); five species in three genera breeding in our region. -
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). -
January 2020.Indd
BROWN PELICAN Photo by Rob Swindell at Melbourne, Florida JANUARY 2020 Editors: Jim Jablonski, Marty Ackermann, Tammy Martin, Cathy Priebe Webmistress: Arlene Lengyel January 2020 Program Tuesday, January 7, 2020, 7 p.m. Carlisle Reservation Visitor Center Gulls 101 Chuck Slusarczyk, Jr. "I'm happy to be presenting my program Gulls 101 to the good people of Black River Audubon. Gulls are notoriously difficult to identify, but I hope to at least get you looking at them a little closer. Even though I know a bit about them, I'm far from an expert in the field and there is always more to learn. The challenge is to know the particular field marks that are most important, and familiarization with the many plumage cycles helps a lot too. No one will come out of this presentation an expert, but I hope that I can at least give you an idea what to look for. At the very least, I hope you enjoy the photos. Looking forward to seeing everyone there!” Chuck Slusarczyk is an avid member of the Ohio birding community, and his efforts to assist and educate novice birders via social media are well known, yet he is the first to admit that one never stops learning. He has presented a number of programs to Black River Audubon, always drawing a large, appreciative gathering. 2019 Wellington Area Christmas Bird Count The Wellington-area CBC will take place Saturday, December 28, 2019. Meet at the McDonald’s on Rt. 58 at 8:00 a.m. The leader is Paul Sherwood. -
Ardea Cinerea (Grey Heron) Family: Ardeidae (Herons and Egrets) Order: Ciconiiformes (Storks, Herons and Ibises) Class: Aves (Birds)
UWU The Online Guide to the Animals of Trinidad and Tobago Behaviour Ardea cinerea (Grey Heron) Family: Ardeidae (Herons and Egrets) Order: Ciconiiformes (Storks, Herons and Ibises) Class: Aves (Birds) Fig. 1. Grey heron, Ardea cinerea. [http://www.google.tt/imgres?imgurl=http://www.bbc.co.uk/lancashire/content/images/2006/06/15/grey_heron, downloaded 14 November 2012] TRAITS. Grey herons are large birds that can be 90-100cm tall and an adult could weigh in at approximately 1.5 kg. They are identified by their long necks and very powerful dagger like bills (Briffett 1992). They have grey plumage with long black head plumes and their neck is white with black stripes on the front. In adults the forehead sides of the head and the centre of the crown are white. In flight the neck is folded back with the wings bowed and the flight feathers are black. Each gender looks alike except for the fact that females have shorter heads (Seng and Gardner 1997). The juvenile is greyer without black markings on the head and breast. They usually live long with a life span of 15-24 years. ECOLOGY. The grey heron is found in Europe, Asia and Africa, and has been recorded as an accidental visitor in Trinidad. Grey herons occur in many different habitat types including savannas, ponds, rivers, streams, lakes and temporary pools, coastal brackish water, wetlands, marsh and swamps. Their distribution may depend on the availability of shallow water (brackish, saline, fresh, flowing and standing) (Briffett 1992). They prefer areas with tall trees for nesting UWU The Online Guide to the Animals of Trinidad and Tobago Behaviour (arboreal rooster and nester) but if trees are unavailable, grey herons may roost in dense brush or undergrowth. -
IUCN-SSC Stork, Ibis and Spoonbill Specialist Group Special Publication 2
IUCN-SSC Stork, Ibis and Spoonbill Specialist Group Special Publication 2 Proceedings of the IX Workshop of the AEWA Eurasian Spoonbill International Expert Group Djerba Island, Tunisia, 14th - 18th November 2018 Editors: Jocelyn Champagnon, Jelena Kralj, Luis Santiago Cano Alonso and K. S. Gopi Sundar Editors-in-Chief, Special Publications, IUCN-SSC Stork, Ibis and Spoonbill Specialist Group K.S. Gopi Sundar, Co-chair IUCN Stork, Ibis and Spoonbill Specialist Group Luis Santiago Cano Alonso, Co-chair IUCN Stork, Ibis and Spoonbill Specialist Group Invited Editors for this issue Jocelyn Champagnon, Tour du Valat, Research Institute for the Conservation of Mediterranean Wetlands, Arles, France Jelena Kralj, Institute of Ornithology, Zagreb, Croatia Expert Review Board Hichem Azafzaf, Association “les Amis des Oiseaux » (AAO/BirdLife Tunisia), Tunisia Petra de Goeij, Royal NIOZ, the Netherlands Csaba Pigniczki, Kiskunság National Park Directorate, Hungary Suggested citation of this publication: Champagnon J., Kralj J., Cano Alonso, L. S. & Sundar, K. S. G. (ed.) 2019. Proceedings of the IX Workshop of the AEWA Eurasian Spoonbill International Expert Group. IUCN-SSC Stork, Ibis and Spoonbill Specialist Group Special Publication 2. Arles, France. ISBN 978-2-491451-00-4. Recommended Citation of a chapter: Marion L. 2019. Recent trends of the breeding population of Spoonbill in France 2012- 2018. Pp 19- 23. In: Champagnon J., Kralj J., Cano Alonso, L. S. & Sundar, K. S. G. (ed.) Proceedings of the IX Workshop of the AEWA Eurasian Spoonbill International Expert Group. IUCN-SSC Stork, Ibis and Spoonbill Specialist Group Special Publication 2. Arles, France. INFORMATION AND WRITING DISCLAIMER The information and opinions expressed in this publication belong to the authors. -
The Grey Heron
Bird Life The Grey Heron t is quite likely that if someone points out a grey heron to you, I you will remember it the next time you see it. The grey heron is a tall bird, usually about 80cm to 1m in height and is common to inland waterways and coasts. Though the grey heron has a loud “fraank” call, it can most often be seen standing silently in shallow water with its long neck outstretched, watching the water for any sign of movement. The grey heron is usually found on its own, although some may feed close together. Their main food is fish, but they will take small mammals, insects, frogs and even young birds. Because of their habit of occasionally taking young birds, herons are not always popular and are often driven away from a feeding area by intensive mobbing. Mobbing is when smaller birds fly aggressively at their predator, in this case the heron, in order to defend their nests or their lives. Like all herons, grey herons breed in a colony called a heronry. They mostly nest in tall trees and bushes, but sometimes they nest on the ground or on ledge of rock by the sea. Nesting starts in February,when the birds perform elaborate displays and make noisy callings. They lay between 3-5 greenish-blue eggs, often stained white by the birds’ droppings. Once hatched, the young © Illustration: Audrey Murphy make continuous squawking noises as they wait to be fed by their parents. And though it doesn’t sound too pleasant, the parent Latin Name: Ardea cinerea swallows the food and brings it up again at the nest, where the Irish Name: Corr réisc young put their bills right inside their parents mouth in order to Colour: Grey back, white head and retrieve it! neck, with a black crest on head. -
Bird Vulnerability Assessments
Assessing the vulnerability of native vertebrate fauna under climate change, to inform wetland and floodplain management of the River Murray in South Australia: Bird Vulnerability Assessments Attachment (2) to the Final Report June 2011 Citation: Gonzalez, D., Scott, A. & Miles, M. (2011) Bird vulnerability assessments- Attachment (2) to ‘Assessing the vulnerability of native vertebrate fauna under climate change to inform wetland and floodplain management of the River Murray in South Australia’. Report prepared for the South Australian Murray-Darling Basin Natural Resources Management Board. For further information please contact: Department of Environment and Natural Resources Phone Information Line (08) 8204 1910, or see SA White Pages for your local Department of Environment and Natural Resources office. Online information available at: http://www.environment.sa.gov.au Permissive Licence © State of South Australia through the Department of Environment and Natural Resources. You may copy, distribute, display, download and otherwise freely deal with this publication for any purpose subject to the conditions that you (1) attribute the Department as the copyright owner of this publication and that (2) you obtain the prior written consent of the Department of Environment and Natural Resources if you wish to modify the work or offer the publication for sale or otherwise use it or any part of it for a commercial purpose. Written requests for permission should be addressed to: Design and Production Manager Department of Environment and Natural Resources GPO Box 1047 Adelaide SA 5001 Disclaimer While reasonable efforts have been made to ensure the contents of this publication are factually correct, the Department of Environment and Natural Resources makes no representations and accepts no responsibility for the accuracy, completeness or fitness for any particular purpose of the contents, and shall not be liable for any loss or damage that may be occasioned directly or indirectly through the use of or reliance on the contents of this publication. -
Wood-Stork-2005.Pdf
WOOD STORK Mycteria americana Photo of adult wood stork in landing posture and chicks in Close-up photo of adult wood stork. nest. Photo courtesy of USFWS/Photo by George Gentry Photo courtesy of U.S. Army Corps of Engineers. FAMILY: Ciconiidae STATUS: Endangered - U.S. Breeding Population (Federal Register, February 28, 1984) [Service Proposed for status upgrade to Threatened, December 26, 2013] DESCRIPTION: Wood storks are large, long-legged wading birds, about 45 inches tall, with a wingspan of 60 to 65 inches. The plumage is white except for black primaries and secondaries and a short black tail. The head and neck are largely unfeathered and dark gray in color. The bill is black, thick at the base, and slightly decurved. Immature birds have dingy gray feathers on their head and a yellowish bill. FEEDING HABITS: Small fish from 1 to 6 inches long, especially topminnows and sunfish, provide this bird's primary diet. Wood storks capture their prey by a specialized technique known as grope-feeding or tacto-location. Feeding often occurs in water 6 to 10 inches deep, where a stork probes with the bill partly open. When a fish touches the bill it quickly snaps shut. The average response time of this reflex is 25 milliseconds, making it one of the fastest reflexes known in vertebrates. Wood storks use thermals to soar as far as 80 miles from nesting to feeding areas. Since thermals do not form in early morning, wood storks may arrive at feeding areas later than other wading bird species such as herons. -
Roseate Spoonbill Breeding in Camden County: a First State Nesting Record for Georgia
vol. 76 • 3 – 4 THE ORIOLE 65 ROSEATE SPOONBILL BREEDING IN CAMDEN COUNTY: A FIRST STATE NESTING RECORD FOR GEORGIA Timothy Keyes One Conservation Way Brunswick, GA 31520 [email protected] Chris Depkin One Conservation Way Brunswick, GA 31520 [email protected] Jessica Aldridge 6222 Charlie Smith Sr. Hwy St. Marys, GA 31558 [email protected] Introduction We report the northernmost breeding record of Roseate Spoonbill (Platalea ajaja) on the Atlantic Coast of the U.S. Nesting activity has been suspected in Georgia for at least 5 years, but was first confirmed in June 2011 at a large wading bird colony in St. Marys, Camden County, Georgia. Prior to this record, the furthest northern breeding record for Roseate Spoonbill was in St. Augustine, St. John’s County, Florida, approximately 100 km to the south. This record for Georgia continues a trend of northward expansion of Roseate Spoonbill post-breeding dispersal and breeding ranges. Prior to the plume-hunting era of the mid to late 1800s, the eastern population of Roseate Spoonbill was more abundant and widespread than it is today (Dumas 2000), breeding across much of south Florida. Direct persecution and collateral disturbance by egret plume hunters led to a significant range contraction between 1850 and the 1890s (Allen 1942), limiting the eastern population of Roseate Spoonbills to a few sites in Florida Bay by the 1940s. A low of 15 nesting pairs were documented in 1936 (Powell et al. 1989). By the late 1960s, Roseate Spoonbills began to expand out of Florida Bay, slowly reclaiming some of the territory they had lost. -
Great Egret Ardea Alba
Great Egret Ardea alba Joe Kosack/PGC Photo CURRENT STATUS: In Pennsylvania, the great egret is listed state endangered and protected under the Game and Wildlife Code. Nationally, they are not listed as an endangered/threatened species. All migra- tory birds are protected under the federal Migratory Bird Treaty Act of 1918. POPULATION TREND: The Pennsylvania Game Commission counts active great egret (Ardea alba) nests in every known colony in the state every year to track changes in population size. Since 2009, only two nesting locations have been active in Pennsylvania: Kiwanis Lake, York County (fewer than 10 pairs) and the Susquehanna River’s Wade Island, Dauphin County (fewer than 200 pairs). Both sites are Penn- sylvania Audubon Important Bird Areas. Great egrets abandoned other colonies along the lower Susque- hanna River in Lancaster County in 1988 and along the Delaware River in Philadelphia County in 1991. Wade Island has been surveyed annually since 1985. The egret population there has slowly increased since 1985, with a high count of 197 nests in 2009. The 10-year average count from 2005 to 2014 was 159 nests. First listed as a state threatened species in 1990, the great egret was downgraded to endan- gered in 1999. IDENTIFYING CHARACTERISTICS: Great egrets are almost the size of a great blue heron (Ardea herodias), but white rather than gray-blue. From bill to tail tip, adults are about 40 inches long. The wingspan is 55 inches. The plumage is white, bill yellowish, and legs and feet black. Commonly confused species include cattle egret (Bubulus ibis), snowy egret (Egretta thula), and juvenile little blue herons (Egretta caerulea); however these species are smaller and do not nest regularly in the state. -
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.