Introduction to Observing Birds: the Science of Life-Long Learning
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Using Chick Down Feathers to Estimate Mercury Concentrations In
Environ. Sci. Technol. 2009, 43, 2166–2172 toxicity thresholds potentially could be refined to incorporate Integrating Toxicity Risk in Bird mercury’s in ovo effects on both eggs and chicks. Eggs and Chicks: Using Chick Down After an egg hatches, chicks may still be vulnerable to the effects of residual in ovo mercury exposure, especially shortly Feathers To Estimate Mercury after hatching, when maternally deposited mercury levels are still relatively high. Thereafter, barring especially high Concentrations in Eggs levels of mercury in their diet, chick mercury concentrations rapidly decline as chicks age and dilute their body burden of mercury through growth and depuration of mercury into JOSHUA T. ACKERMAN* AND - COLLIN A. EAGLES-SMITH growing feathers (21 23). Chick mortality associated with mercury contamination often occurs within the first week U.S. Geological Survey, Western Ecological Research Center, after hatching (15-17), indicating that in ovo mercury Davis Field Station, One Shields Avenue, University of California, Davis, California 95616 exposure can influence posthatch survival. Incorporating this early chick mortality into egg toxicity thresholds is hampered by our inability to translate mercury concentrations in chicks Received November 7, 2008. Revised manuscript received to what the equivalent concentrations were in eggs. January 9, 2009. Accepted January 20, 2009. Down feathers of newly hatched chicks are potentially useful tools for estimating mercury concentrations in the eggs from which they hatched. Down feathers are grown in The concentration of mercury (Hg) in eggs that causes ovo during the embryonic phase and, in some species, can contain about 38% of the total body burden of mercury in reduced hatching success is regarded as a critical end point newly hatched chicks (24, 25). -
Conservation Assessment for Red-Shouldered Hawk (Buteo Lineatus) National Forests of North Central States
Conservation Assessment for Red-shouldered Hawk (Buteo lineatus) National Forests of North Central States USDA Forest Service Eastern Region December 2002 Prepared by: John P. Jacobs 2373 Libal St, Green Bay, WI 54301 E-mail: [email protected] jacobs_rs Eugene A. Jacobs Linwood Springs Research Station 1601 Brown Deer Lane, Stevens Point, Wisconsin 54481 E-mail: [email protected] This Conservation Assessment was prepared to compile the published and unpublished information on Red-shouldered Hawks. It does not represent a management decision by the U.S. Forest Service. A Conservation Approach will be developed later and conservation measures incorporated into Forest Plans; public involvement will occur via the NEPA process. Although the best scientific information available was used and subject experts were consulted in the preparation of this document, it is expected that new information will arise. In the spirit of continuous learning and adaptive management, if you have information that will assist in conserving this species, please contact the Eastern Region of the Forest Service Threatened and Endangered Species Program at 310 Wisconsin Avenue, Milwaukee, Wisconsin 53203. Conservation Assessment for Red-shouldered Hawk (Buteo lineatus) 2 Table of Contents 1. Executive Summary ……………………………………………………………. 6 2. Introduction ....................................……………………………………. 7 3. Acknowledgements ................................................................................. 8 4. Nomenclature and Taxonomy ……………………………………………. 8 5. -
Breeding Hand-Reeding Hooded Parrots
Notes on Breeding and Hand-reeding Hooded Parrots by Fred andLyrae Perry Corona, California The hooded parrot (Psephotus chrysopterygius dissimilisJ) is one of the most outstandingly beautiful member ofthe Psephotus genus. This little bird is actually a subspecies ofthe golden- houldered parrot (Psephotus chrysopterygiusJ. The range of the hooded parrot is quite restricted; from the Macarthur River, west to the Apairofgolden-shoulderedparakeets(Psephotus c. chrysopterygius). This is the nominate species ofwhich the hoodedparakeetis a sub-species. The golden-shouldered is seldom if Arnham Land plateau in the orthern everfound in aviculture. Territory of Australia. The wild popu lation is on the decline mo t probably adult female is a oft blue-green overall, this article. In our experience, these due to illegal trapping and variou other with the wing and tail feather being methods have greatly improved the sur man-made and natural disasters. For olive green, the central tail feathers are vival rate ofbaby hooded parrots. these reasons, hoodedparrots are quite also tipped in white, and the vent Hooded parrots in the wild nest in rare in collections today. feathers are a lighter shade of red, or termite mounds from May through The adult male i turquoise blue over salmonpink. The young birds resemble January. The babies hatch with a light mo t of the body, rump and cheeks. the females in coloration. down feather, which wear offquickly, The feathers are highly irridescent, The hooded parrot available to leaving them quite naked. A heavy giving the male a jewel-like appearance. aviculturists today are domestically down feathering would actually be a The wingpatches are bright yellow. -
A Comprehensive Species-Level Molecular Phylogeny of the New World
YMPEV 4758 No. of Pages 19, Model 5G 2 December 2013 Molecular Phylogenetics and Evolution xxx (2013) xxx–xxx 1 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev 5 6 3 A comprehensive species-level molecular phylogeny of the New World 4 blackbirds (Icteridae) a,⇑ a a b c d 7 Q1 Alexis F.L.A. Powell , F. Keith Barker , Scott M. Lanyon , Kevin J. Burns , John Klicka , Irby J. Lovette 8 a Department of Ecology, Evolution and Behavior, and Bell Museum of Natural History, University of Minnesota, 100 Ecology Building, 1987 Upper Buford Circle, St. Paul, MN 9 55108, USA 10 b Department of Biology, San Diego State University, San Diego, CA 92182, USA 11 c Barrick Museum of Natural History, University of Nevada, Las Vegas, NV 89154, USA 12 d Fuller Evolutionary Biology Program, Cornell Lab of Ornithology, Cornell University, 159 Sapsucker Woods Road, Ithaca, NY 14950, USA 1314 15 article info abstract 3117 18 Article history: The New World blackbirds (Icteridae) are among the best known songbirds, serving as a model clade in 32 19 Received 5 June 2013 comparative studies of morphological, ecological, and behavioral trait evolution. Despite wide interest in 33 20 Revised 11 November 2013 the group, as yet no analysis of blackbird relationships has achieved comprehensive species-level sam- 34 21 Accepted 18 November 2013 pling or found robust support for most intergeneric relationships. Using mitochondrial gene sequences 35 22 Available online xxxx from all 108 currently recognized species and six additional distinct lineages, together with strategic 36 sampling of four nuclear loci and whole mitochondrial genomes, we were able to resolve most relation- 37 23 Keywords: ships with high confidence. -
The Molecular Evolution of Feathers with Direct Evidence from Fossils
The molecular evolution of feathers with direct evidence from fossils Yanhong Pana,1, Wenxia Zhengb, Roger H. Sawyerc, Michael W. Penningtond, Xiaoting Zhenge,f, Xiaoli Wange,f, Min Wangg,h, Liang Hua,i, Jingmai O’Connorg,h, Tao Zhaoa, Zhiheng Lig,h, Elena R. Schroeterb, Feixiang Wug,h, Xing Xug,h, Zhonghe Zhoug,h,i,1, and Mary H. Schweitzerb,j,1 aChinese Academy of Sciences Key Laboratory of Economic Stratigraphy and Palaeogeography, Nanjing Institute of Geology and Palaeontology and Center for Excellence in Life and Paleoenvironment, Chinese Academy of Sciences, Nanjing 210008, China; bDepartment of Biological Sciences, North Carolina State University, Raleigh, NC 27695; cDepartment of Biological Sciences, University of South Carolina, Columbia, SC 29205; dAmbioPharm Incorporated, North Augusta, SC 29842; eInstitute of Geology and Paleontology, Lingyi University, Lingyi City, 27605 Shandong, China; fShandong Tianyu Museum of Nature, Pingyi, 273300 Shandong, China; gCAS Key Laboratory of Vertebrate Evolution and Human Origins of the Chinese Academy of Sciences, Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences, 100044 Beijing, China; hCenter for Excellence in Life and Paleoenvironment, Chinese Academy of Sciences, 100044 Beijing, China; iCollege of Earth and Planetary Sciences, University of Chinese Academy of Sciences, 100049 Beijing, China; and jNorth Carolina Museum of Natural Sciences, Raleigh, NC 27601 Contributed by Zhonghe Zhou, December 15, 2018 (sent for review September 12, 2018; reviewed by Dominique G. Homberger and Chenxi Jia) Dinosaur fossils possessing integumentary appendages of various feathers in Anchiornis, barbules that interlock to form feather morphologies, interpreted as feathers, have greatly enhanced our vanes critical for flight have not been identified yet (12). -
Fraga Ms-706.Fm
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by CONICET Digital SHORT COMMUNICATIONS ORNITOLOGIA NEOTROPICAL 19: 299–303, 2008 © The Neotropical Ornithological Society NOTES ON THE NESTING OF CHOPI BLACKBIRDS (GNORIMOPSAR CHOPI) IN ARGENTINA AND PARAGUAY, WITH DATA ON COOPERATIVE BREEDING AND BROOD PARASITISM BY SCREAMING COWBIRDS (MOLOTHRUS RUFOAXILLARIS) Rosendo M. Fraga CICYTTP, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Matteri y España, (3105) Diamante, Entre Ríos, Argentina. E-mail: [email protected] Notas sobre la nidificación del Chopí (Gnorimopsar chopi) en Argentina y Paraguay, con datos de cría cooperativa y de parasitismo de cría por el Tordo Pico Corto (Molothrus rufoaxillaris). Key words: Chopi Blackbirds, Gnorimopsar chopi, nesting, cooperative breeding, Screaming Cowbird, Molothrus rufoaxillaris. The Chopi Blackbird (Gnorimopsar chopi) is an northeastern Argentina (Corrientes and Mis- icterid endemic to South America (Jaramillo iones provinces) and Paraguay, between 1995 & Burke 1999) and a member of the South and 2007. My data show this icterid to be a American quiscaline clade, a monophyletic cooperative breeder (Brown 1987), as individ- group defined by DNA data (Johnson & uals other than a single pair aid in chick care. Lanyon 1999, Cadena et al. 2004). This icterid Also, I add further information on its host- is found from northeastern Brazil and south- parasite interactions with Screaming Cow- eastern Peru to northern Argentina and Uru- birds (Molothrus rufoaxillaris) in Argentina and guay (Jaramillo & Burke 1999). It is usually Paraguay (Sick 1985, Fraga 1996). subdivided into three subspecies with consid- I obtained most of my information on erable variation in body size (Jaramillo & Chopi Blackbirds while carrying field research Burke 1999), but only the nominate subspe- on endangered grassland birds from eastern cies occurs in eastern Argentina and Paraguay. -
Rare Feeding Behavior of Great-Tailed Grackles (Quiscalus Mexicanus) in the Extreme Habitat of Death Valley
The Open Ornithology Journal, 2010, 3, 101-104 101 Open Access Rare Feeding Behavior of Great-Tailed Grackles (Quiscalus mexicanus) in the Extreme Habitat of Death Valley Stefanie Grabrucker and Andreas M. Grabrucker* University Ulm, 89069 Ulm, Germany Abstract: During the twentieth century, the Great-tailed Grackle (Quiscalus mexicanus) underwent a rapid and large- scale range expansion, extending its northern limits from Texas in 1900 to 21 states in the US and 3 Canadian provinces by the end of the century. This explosive growth correlated with human-induced habitat changes. To investigate adaptations that might explain their expansion into even extreme habitats, a small number of Great-tailed Grackles were observed in Death Valley, CA. We noticed that these birds displayed a rare feeding behavior, i.e. picking dead insects from the license plates of parked vehicles. All birds used the same technique in obtaining the food and the behavior was displayed by both males and females. It was estimated that this food resource has a major contribution to the daily food intake. No other bird species sharing the same habitat showed this behavior although American crows (Corvus brachyrhynchos) had the possibility to watch the Great-tailed Grackles behavior. Keywords: Great-tailed Grackle, Feeding behavior, Death Valley, Adaptation, License plate. INTRODUCTION recorded with a temperature above 37,8° C. The summer of 1996 had 40 days over 48,9° C, and 105 days over 43,4° C Great-tailed Grackles (Quiscalus mexicanus) were [16]. Heat exposure significantly decreases live weight gain, investigated with regard to their potential to adapt and feed efficiency, and carcass weight in birds like quails survive in extreme habitats like Death Valley, CA. -
Pattern and Chronology of Prebasic Molt for the Wood Thrush and Its Relation to Reproduction and Migration Departure
Wilson Bull., 110(3), 1998, pp. 384-392 PATTERN AND CHRONOLOGY OF PREBASIC MOLT FOR THE WOOD THRUSH AND ITS RELATION TO REPRODUCTION AND MIGRATION DEPARTURE J. H. VEGA RIVERA,1,3 W. J. MCSHEA,* J. H. RAPPOLE, AND C. A. HAAS ’ ABSTRACT-Documentation of the schedule and pattern of molt and their relation to reproduction and migration departure are important, but often neglected, areas of knowledge. We radio-tagged Wood Thrushes (Hylocichlu mustelina), and monitored their movements and behavior on the U.S. Marine Corps Base, Quantico, Virginia (38” 40 ’ N, 77” 30 ’ W) from May-Oct. of 1993-1995. The molt period in adults extended from late July to early October. Molt of flight feathers lasted an average of 38 days (n = 17 birds) and there was no significant difference in duration between sexes. In 21 observed and captured individuals, all the rectrices were lost simultaneously or nearly so, and some individuals dropped several primaries over a few days. Extensive molt in Wood Thrushes apparently impaired flight efficiency, and birds at this stage were remarkably cautious and difficult to capture and observe. All breeding individuals were observed molting l-4 days after fledgling independence or last-clutch predation, except for one pair that began molt while still caring for fledglings. Our data indicate that energetics or flight efficiency constraints may dictate a separation of molt and migration. We did not observe Wood Thrushes leaving the Marine Base before completion of flight-feather molt. Departure of individuals with molt in body and head, however, was common. We caution against interpreting the lack of observations or captures of molting individuals on breeding sites as evidence that birds actually have left the area. -
Didelphis Virginiana) As a Host for Sarcocystis Debonei from Cowbirds (Molothrus Ater) and Grackles (Cassidix Mexicanus, Quiscalus Quiscula)
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications from the Harold W. Manter Laboratory of Parasitology Parasitology, Harold W. Manter Laboratory of 4-1978 The Opossum (Didelphis virginiana) as a Host for Sarcocystis debonei from Cowbirds (Molothrus ater) and Grackles (Cassidix mexicanus, Quiscalus quiscula) Donald Duszynski University of New Mexico, [email protected] Edith D. Box University of Texas Medical Branch Follow this and additional works at: https://digitalcommons.unl.edu/parasitologyfacpubs Part of the Parasitology Commons Duszynski, Donald and Box, Edith D., "The Opossum (Didelphis virginiana) as a Host for Sarcocystis debonei from Cowbirds (Molothrus ater) and Grackles (Cassidix mexicanus, Quiscalus quiscula)" (1978). Faculty Publications from the Harold W. Manter Laboratory of Parasitology. 129. https://digitalcommons.unl.edu/parasitologyfacpubs/129 This Article is brought to you for free and open access by the Parasitology, Harold W. Manter Laboratory of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Publications from the Harold W. Manter Laboratory of Parasitology by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. J. Parasitol., 64(2), 1978, pp. 326-329 ? American Society of Parasitologists 1978 THE OPOSSUM (DIDELPHISVIRGINIANA) AS A HOST FOR SARCOCYSTISDEBONEI FROM COWBIRDS (MOLOTHRUS ATER) AND GRACKLES(CASSIDIX MEXICANUS, QUISCALUS QUISCULA) Donald W. Duszynski* and Edith D. Boxt ABSTRACT: Sarcocystis-infected muscles from ducks, cowbirds, and grackles were fed to cats, opossums, rats, and a dog. Only the opossum (Didelphis virginiana) was a suitable definitive host. All opossums that were fed Sarcocystis-infected cowbirds (Molothrus ater) and grackles (Cassidix mexicanus and Quiscalus quiscula) passed sporocysts in their feces. -
Birds and Mammals)
6-3.1 Compare the characteristic structures of invertebrate animals... and vertebrate animals (...birds and mammals). Also covers: 6-1.1, 6-1.2, 6-1.5, 6-3.2, 6-3.3 Birds and Mammals sections More Alike than Not! Birds and mammals have adaptations that 1 Birds allow them to live on every continent and in 2 Mammals every ocean. Some of these animals have Lab Mammal Footprints adapted to withstand the coldest or hottest Lab Bird Counts conditions. These adaptations help to make Virtual Lab How are birds these animal groups successful. adapted to their habitat? Science Journal List similar characteristics of a mammal and a bird. What characteristics are different? 254 Theo Allofs/CORBIS Start-Up Activities Birds and Mammals Make the following Foldable to help you organize information about the Bird Gizzards behaviors of birds and mammals. You may have observed a variety of animals in your neighborhood. Maybe you have STEP 1 Fold one piece of paper widthwise into thirds. watched birds at a bird feeder. Birds don’t chew their food because they don’t have teeth. Instead, many birds swallow small pebbles, bits of eggshells, and other hard materials that go into the gizzard—a mus- STEP 2 Fold down 2.5 cm cular digestive organ. Inside the gizzard, they from the top. (Hint: help grind up the seeds. The lab below mod- From the tip of your els the action of a gizzard. index finger to your middle knuckle is about 2.5 cm.) 1. Place some cracked corn, sunflower seeds, nuts or other seeds, and some gravel in an STEP 3 Fold the rest into fifths. -
Species List February 20 ‒ 28, 2019 | Written by Bob Meinke
Southern Belize: Birding & Nature | Species List February 20 ‒ 28, 2019 | Written by Bob Meinke Guide Bob Meinke, with expert local lodge naturalists Marvin and Steven, and 9 participants: Kelly, Isaac, Lenore, Harold, Cindy, Richelle, Beth, Nancy, and Joe SUMMARY We enjoyed a scenic and productive trip, starting with the vast freshwater wetlands at Crooked Tree Lagoon, transitioning on to the montane woodlands of the Mountain Pine Ridge, and ending our tour in the broadleaf forests and mangroves of Toledo District at the southern tip of Belize. Working our way down the length of the country increased our exposure to a wide range of habitats, and with it came a nice assortment of resident and migrant bird species as well as other wildlife. Highlights among the resident species included King Vulture, Bare-crowned Antbird, Black-and-white Owl, Yucatan Jay, White-winged Becard, Ruddy Woodcreeper, Eye-ringed Flatbill, Violet Sabrewing, three species of Trogon, and five species of Kingfisher (with multiple, close-in views of American Pygmy a surprising bonus). And while not unexpected, Keel-billed Toucan, Collared Aracari, Bare-throated Tiger Heron, Montezuma Oropendola, Golden -headed Tanager, Barred Antshrike, and Squirrel Cuckoo were all exquisite reminders of the rich colors and morphological diversity that characterize the avifauna of the Neotropics. North American migrants were also plentiful during our visit, and among the many warblers encountered, Blue-winged, Worm-eating, and Prothonotary stood out among the 21 overwintering species we recorded, most of which were just entering full breeding plumage as they readied for their journey north to the U.S. -
The Physical Structure, Optical Mechanics and Aesthetics of the Peacock Tail Feathers
© 2002 WIT Press, Ashurst Lodge, Southampton, SO40 7AA, UK. All rights reserved. Web: www.witpress.com Email [email protected] Paper from: Design and Nature, CA Brebbia, L Sucharov & P Pascola (Editors). ISBN 1-85312-901-1 The physical structure, optical mechanics and aesthetics of the peacock tail feathers S.C. Burgess Department of Mechanical Engineering, University of Bristol, University Walk, Bristol, BS8 I TR, UK Abstract The peacock tail feathers have no flight or thermal function but have the sole purpose of providing an attractive display. The peacock tail produces colours by thin-film interference. There is a very high level of optimum design in the peacock feathers including optimum layer thickness, multi layers, precision co- ordination and dark background colour, This paper analyses the structure and beauty of the peacock tail. 1 Introduction Aesthetic beauty in appearance is produced by attributes such as patterns, brightness, variety, curves, blending or any combination of such attributes. Beauty is so important in engineering design that there is a whole subject called aesthetics which defines how beauty can be added to man-made products’, An object can have two types of beauty: inherent beauty and added beauty, Inherent beauty is a beauty that exists as a hi-product of mechanical design, In contrast, added beauty is a type of beauty which has the sole purpose of providing a beautiful display. These two types of beauty can be seen in man-made products like buildings and bridges. An example of inherent beauty is found in the shape of a suspension bridge, A suspension bridge has a curved cable structure because this is an efficient way of supporting a roadway.