Roseate Spoonbill
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GEESE, SWANS & DUCKS __ Double-crested Cormorant __ Peregrine Falcon __ Laughing Gull __ Franklin’s Gull __ Blk.-bellied Whistling-Duck ANHINGAS RAILS, GALLINULES & __ Ring-billed Gull __ Fulvous Whistling-Duck __ Anhinga COOTS __ Herring Gull __ Grtr. White-fronted Goose __ King Rail __ Least Tern __ Snow Goose PELICANS __ Virginia Rail __ Caspian Tern __ Ross’s Goose __ American White Pelican __ Sora __ Black Tern __ Cackling Goose __ Purple Gallinule __ Forster’s Tern __ Canada Goose BITTERNS & HERONS __ Common Gallinule __ Tundra Swan __ American Bittern __ American Coot PIGEONS & DOVES __ Wood Duck __ Least Bittern __ Rock Pigeon __ Gadwall __ Great Blue Heron CRANES __ Eurasian Collared-Dove __ American Wigeon __ Great Egret __ Sandhill Crane __ White-winged Dove __ American Black Duck __ Snowy Egret __ Mourning Dove BIRD CHECKLIST __ Mallard __ Little Blue Heron PLOVERS __ Blue-winged Teal __ Tricolored Heron __ Black-bellied Plover CUCKOOS & ANIS __ Northern Shoveler __ Cattle Egret __ American Golden-Plover __ Yellow-billed Cuckoo __ Northern Pintail __ Green Heron __ Semipalmated Plover __ Black-billed Cuckoo ara Wildlife is a great place to see the __ Green-winged Teal __ Black-crowned Night-Heron __ Killdeer beautiful and varied bird life of the __ Canvasback __ Yell.-crowned Night-Heron BARN OWLS __ Redhead STILTS & AVOCETS __ Barn Owl Mississippi River valley. Its bottomland __ Ring-necked Duck IBISES & SPOONBILLS __ Black-necked Stilt Tforests, wetlands, river shoreline, sloughs and __ Greater Scaup __ White Ibis __ American Avocet TYPICAL OWLS other habitats harbor Wood Storks, Roseate __ Lesser Scaup __ Glossy Ibis __ Eastern Screech-Owl __ Long-tailed Duck __ White-faced Ibis SANDPIPERS __ Great Horned Owl Spoonbills, Bald Eagles, Prothonotary __ Bufflehead __ Roseate Spoonbill __ Spotted Sandpiper __ Barred Owl Warblers, Painted Buntings and many other __ Common Goldeneye __ Solitary Sandpiper __ Short-eared Owl __ Hooded Merganser VULTURES __ Greater Yellowlegs species. -
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. -
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. -
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. -
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 -
Flocking of V-Shaped and Echelon Northern Bald Ibises with Different Wingspans: Repositioning and Energy Saving
Flocking of V-shaped and Echelon Northern Bald Ibises with Different Wingspans: Repositioning and Energy Saving Amir Mirzaeinia1, Mehdi Mirzaeinia2, Mostafa Hassanalian3* V-shaped and echelon formations help migratory birds to consume less energy for migration. As the case study, the formation flight of the Northern Bald Ibises is considered to investigate different effects on their flight efficiency. The effects of the wingtip spacing and wingspan are examined on the individual drag of each Ibis in the flock. Two scenarios are considered in this study, (1) increasing and (2) decreasing wingspans toward the tail. An algorithm is applied for replacement mechanism and load balancing of the Ibises during their flight. In this replacing mechanism, the Ibises with the highest value of remained energy are replaced with the Ibises with the lowest energy, iteratively. The results indicate that depending on the positions of the birds with various sizes in the flock, they consume a different level of energy. Moreover, it is found that also small birds have the chance to take the lead during the flock. I. Introduction There are 1800 species of birds that migrate through seasonal long-distance routes from hundreds up to several thousand kilometers1. For example, Bar-tailed godwits as one of the non-stop migratory birds travel for 11600 km1,2. Canada Geese with an average speed of about 18 m/s migrate for 3,200 to 4,800 Km in a single day if the weather is good44. The Arctic terns migrate from the Arctic to the Antarctic1. Besides the mentioned migratory birds, other bird species including pelicans, swans, cormorants, cranes, and Ibis migrate in an echelon or V-shaped formations1. -
Indiana Division of Fish & Wildlife's Animal Information Series: Paddlefish
Indiana Division of Fish & Wildlife’s Animal Information Series Paddlefish (Polyodon spathula) Do they have any other names? Paddlefish are also called spoonbill, spoonbill cat, shovelnose cat, and boneless cat. Why are they called paddlefish? They are called paddlefish because of their paddle-like nose. Polyodon is Greek for “many tooth” in reference to the numerous long gill rakers and spathula is Latin for “spatula” or “blade.” What do they look like? Paddlefish are shark-like fish with long, paddle-shaped snouts. They have large mouths, without teeth, that are located far back on the underside of the head. Paddlefish have many gill rakers (filaments used to filter food from the water) that are long and slender. The eyes are small and just above the front edge of the mouth. The rear margin of the gill cover is long and pointed into a fleshy flap. The tail is deeply lobed with the upper lobe longer than the lower lobe. The skin is without scales and the skeleton is made of cartilage. Paddlefish are bluish-gray to black on the upper parts and light gray to white on the belly. Photo Credit: Duane Raver, USFWS Where do they live in Indiana? Paddlefish are rare to occasional in Indiana and they live in large rivers. What kind of habitat do they need? A paddlefish needs very specific habitat conditions to meet its needs. During most of its life it lives in quiet or slow-flowing waters rich in the microscopic life (zooplankton) on which it feeds. However, it must have access to a large, free-flowing river with gravel bars that flood frequently during its spawning season. -
Developing a Research Network on Glossy Ibis, a Neglected Cosmopolitan Species
Developing a research network on Glossy ibis, a neglected cosmopolitan species Álvaro Arenas Patiño © 2014 The Project in a nutshell The Glossy ibis (Plegadis falcinellus) is the only cosmopolitan species of the Threskiornithidae family (ibis and spoonbills) and among the most widely distributed bird species in the world ([1] see map at the bottom of the document). Nonetheless, no knowledge exists on the intraspecific phylogeny and very little is known about the (meta)populations dynamics. We aim to fill this gap by setting up a research network and by implementing modern analytical tools (e.g. molecular and statistical) we nowadays dispose of. Some puzzling aspects of Glossy ibis abundance and distribution Little is known about the movement ecology of this species especially when focusing on a large spatial scale. In most ornithology books the Glossy ibis is described as migratory with nomadic elements [2] with populations at tropics being more sedentary than others. However, references are rarely provided and, to the best of our knowledge, only a few data have been ever collected on the Glossy ibis dispersal behavior. According to historical records, breeding was very rare in W Europe while common in North Africa and S Spain before the 20th century when it became almost absent in all these regions [3–5]. In 1996 seven pairs settled at Doñana, a wetland area in SW Spain, from where the species begun an astonishing population increase reaching about 8,000 pairs in current times [6,7]. Since then, the Glossy ibis has started to colonize other areas in W Europe and the Mediterranean Basin from where it had been absent for decades or even had never been recorded as a breeder species. -
New Observations of the Andean Ibis (Theristicus Branickii
SIT Graduate Institute/SIT Study Abroad SIT Digital Collections Independent Study Project (ISP) Collection SIT Study Abroad Fall 12-1-2014 New Observations of the Andean Ibis (Theristicus branickii, Threskiornithidae): Distribution, Movements, and Behavior Near Volcán Antisana Benjamin West SIT Study Abroad Follow this and additional works at: https://digitalcollections.sit.edu/isp_collection Part of the Latin American Studies Commons, Other Ecology and Evolutionary Biology Commons, Population Biology Commons, and the Zoology Commons Recommended Citation West, Benjamin, "New Observations of the Andean Ibis (Theristicus branickii, Threskiornithidae): Distribution, Movements, and Behavior Near Volcán Antisana" (2014). Independent Study Project (ISP) Collection. 2019. https://digitalcollections.sit.edu/isp_collection/2019 This Article is brought to you for free and open access by the SIT Study Abroad at SIT Digital Collections. It has been accepted for inclusion in Independent Study Project (ISP) Collection by an authorized administrator of SIT Digital Collections. For more information, please contact [email protected]. New Observations of the Andean Ibis (Theristicus branickii , Threskiornithidae): Distribution, Movements, and Behavior Near Volcán Antisana West, Benjamin M. Academic Directors: Silva, Xavier and Robayo, Javier Project Advisor: Williamson, Jessie Bowdoin College Biology South America, Ecuador, Napo Province, Reserva Ecológica Antisana Submitted in partial fulfillment of the requirements for Ecuador: Comparative Ecology and Conservation, SIT Study Abroad, Fall 2014 SIT Ecuador: Ecology, Fall 2014 West Abstract The Andean Ibis (Theristicus branickii ) of the highland grasslands of Ecuador, Peru, and Bolivia is listed globally as Near Threatened and Critically Endangered in Ecuador. The Ecuadorian population is estimated at 100 individuals and is restricted to the vicinities of Volcán Antisana and Volcán Cotopaxi. -
The Bare Head of the Northern Bald Ibis (Geronticus Eremita) Fulfills a Thermoregulatory Function Ismael Galván1* , Daniel Palacios2 and Juan José Negro1
Galván et al. Frontiers in Zoology (2017) 14:15 DOI 10.1186/s12983-017-0201-5 RESEARCH Open Access The bare head of the Northern bald ibis (Geronticus eremita) fulfills a thermoregulatory function Ismael Galván1* , Daniel Palacios2 and Juan José Negro1 Abstract Background: Dark pigments provide animals with several adaptive benefits such as protection against ultraviolet (UV) radiation and mechanical abrasion, but may also impose several constraints like a high absorbance of solar radiation. Endotherms, with relatively constant and high body temperatures, may be especially prone to thermoregulatory limitations if dark coloured and inhabiting hot environments. It is therefore expected that adaptations have specifically evolved because of these limitations. Bare, highly vascularised head skin may have evolved in birds with dark plumage from hot geographical regions because of favouring heat dissipation. Using the Northern bald ibis (Geronticus eremita) as a model species, we measured the surface temperature (Tsurf) of the head, the bill and the black feathered body of 11 birds along ambient temperatures (Ta) ranging from 21 to 42.5 °C employing thermal imaging. Results: While Tsurf of the bill and the feathered body was only slightly above Ta, head Tsurf was considerably higher, by up to 12 °C. Estimated values of heat loss followed similar variations. We also found that the red colour intensity of the head of ibises increased with head Tsurf, suggesting that birds are capable of controlling blood flow and the thermoregulatory function of the head. Conclusions: These findings are consistent with the hypothesis that bare skin has evolved in dark pigmented birds inhabiting hot environments because of their ability to dissipate heat. -
SHOREBIRDS (Charadriiformes*) CARE MANUAL *Does Not Include Alcidae
SHOREBIRDS (Charadriiformes*) CARE MANUAL *Does not include Alcidae CREATED BY AZA CHARADRIIFORMES TAXON ADVISORY GROUP IN ASSOCIATION WITH AZA ANIMAL WELFARE COMMITTEE Shorebirds (Charadriiformes) Care Manual Shorebirds (Charadriiformes) Care Manual Published by the Association of Zoos and Aquariums in association with the AZA Animal Welfare Committee Formal Citation: AZA Charadriiformes Taxon Advisory Group. (2014). Shorebirds (Charadriiformes) Care Manual. Silver Spring, MD: Association of Zoos and Aquariums. Original Completion Date: October 2013 Authors and Significant Contributors: Aimee Greenebaum: AZA Charadriiformes TAG Vice Chair, Monterey Bay Aquarium, USA Alex Waier: Milwaukee County Zoo, USA Carol Hendrickson: Birmingham Zoo, USA Cindy Pinger: AZA Charadriiformes TAG Chair, Birmingham Zoo, USA CJ McCarty: Oregon Coast Aquarium, USA Heidi Cline: Alaska SeaLife Center, USA Jamie Ries: Central Park Zoo, USA Joe Barkowski: Sedgwick County Zoo, USA Kim Wanders: Monterey Bay Aquarium, USA Mary Carlson: Charadriiformes Program Advisor, Seattle Aquarium, USA Sara Perry: Seattle Aquarium, USA Sara Crook-Martin: Buttonwood Park Zoo, USA Shana R. Lavin, Ph.D.,Wildlife Nutrition Fellow University of Florida, Dept. of Animal Sciences , Walt Disney World Animal Programs Dr. Stephanie McCain: AZA Charadriiformes TAG Veterinarian Advisor, DVM, Birmingham Zoo, USA Phil King: Assiniboine Park Zoo, Canada Reviewers: Dr. Mike Murray (Monterey Bay Aquarium, USA) John C. Anderson (Seattle Aquarium volunteer) Kristina Neuman (Point Blue Conservation Science) Sarah Saunders (Conservation Biology Graduate Program,University of Minnesota) AZA Staff Editors: Maya Seaman, MS, Animal Care Manual Editing Consultant Candice Dorsey, PhD, Director of Animal Programs Debborah Luke, PhD, Vice President, Conservation & Science Cover Photo Credits: Jeff Pribble Disclaimer: This manual presents a compilation of knowledge provided by recognized animal experts based on the current science, practice, and technology of animal management. -
Coastal Wetlands Species Fact Sheet
TEXAS PARKS AND WILDLIFE Whooping Crane Grus americana TPWD PHOTO Whooping cranes are one of the rarest bird species in North America. Although they breed in Canada during the summer months, whooping cranes migrate to Texas’ coastal plains near Rockport for the winter months. COASTAL WETLANDS Whooping Crane Grus americana APPEARANCE BEHAVIOR Height: 5 feet (1.5 m) Whooping cranes begin their fall migration south to Texas in Wingspan: 7.5 feet (2.3 m) mid-September and begin the spring migration north to Canada in late March or early April. They mate for life, but will accept a Distinguishing Characteristics new mate if one dies. The mated pair shares brooding duties; • White with rust-colored patches on top and back of head either the male or the female is always on the nest. The hatch- • Black feathers on both sides of the head lings will stay with their parents throughout their first winter, • Yellow eyes and separate when the spring migration begins. The sub-adults • Primary wing feathers are black but are visible only in flight. form groups and travel together. • Long, black legs and bills NOW YOU KNOW! LIFE HISTORY • Whooping cranes live in “families” with two adult birds, a Range: Limited in Texas to the migratory flyway male and a female, and one or two of their young. Whooping and coastal plain around Aransas. cranes migrate more than 2,400 miles a year. Diet: Crabs, clams, crayfish, snails, minnows, • As many as 1,400 whooping cranes migrated across North frogs, larval insects and leeches; occa- America in the mid-1800s.