Nutrition Guidelines for Ostriches and Emus
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Avian Crop Function–A Review
Ann. Anim. Sci., Vol. 16, No. 3 (2016) 653–678 DOI: 10.1515/aoas-2016-0032 AVIAN CROP function – A REVIEW* * Bartosz Kierończyk1, Mateusz Rawski1, Jakub Długosz1, Sylwester Świątkiewicz2, Damian Józefiak1♦ 1Department of Animal Nutrition and Feed Management, Poznań University of Life Sciences, Wołyńska 33, 60-637 Poznań, Poland 2Department of Animal Nutrition and Feed Science, National Research Institute of Animal Production, 32-083 Balice n. Kraków, Poland ♦Corresponding author: [email protected] Abstract The aim of this review is to present and discuss the anatomy and physiology of crop in different avian species. The avian crop (ingluvies) present in most omnivorous and herbivorous bird spe- cies, plays a major role in feed storage and moistening, as well as functional barrier for pathogens through decreasing pH value by microbial fermentation. Moreover, recent data suggest that this gastrointestinal tract segment may play an important role in the regulation of the innate immune system of birds. In some avian species ingluvies secretes “crop milk” which provides high nutri- ents and energy content for nestlings growth. The crop has a crucial role in enhancing exogenous enzymes efficiency (for instance phytase and microbial amylase,β -glucanase), as well as the activ- ity of bacteriocins. Thus, ingluvies may have a significant impact on bird performance and health status during all stages of rearing. Efficient use of the crop in case of digesta retention time is es- sential for birds’ growth performance. Thus, a functionality of the crop is dependent on a number of factors, including age, dietary factors, infections as well as flock management. -
Ostrich Production Systems Part I: a Review
11111111111,- 1SSN 0254-6019 Ostrich production systems Food and Agriculture Organization of 111160mmi the United Natiorp str. ro ucti s ct1rns Part A review by Dr M.M. ,,hanawany International Consultant Part II Case studies by Dr John Dingle FAO Visiting Scientist Food and , Agriculture Organization of the ' United , Nations Ot,i1 The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. M-21 ISBN 92-5-104300-0 Reproduction of this publication for educational or other non-commercial purposes is authorized without any prior written permission from the copyright holders provided the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited without written permission of the copyright holders. Applications for such permission, with a statement of the purpose and extent of the reproduction, should be addressed to the Director, Information Division, Food and Agriculture Organization of the United Nations, Viale dells Terme di Caracalla, 00100 Rome, Italy. C) FAO 1999 Contents PART I - PRODUCTION SYSTEMS INTRODUCTION Chapter 1 ORIGIN AND EVOLUTION OF THE OSTRICH 5 Classification of the ostrich in the animal kingdom 5 Geographical distribution of ratites 8 Ostrich subspecies 10 The North -
71St Annual Meeting Society of Vertebrate Paleontology Paris Las Vegas Las Vegas, Nevada, USA November 2 – 5, 2011 SESSION CONCURRENT SESSION CONCURRENT
ISSN 1937-2809 online Journal of Supplement to the November 2011 Vertebrate Paleontology Vertebrate Society of Vertebrate Paleontology Society of Vertebrate 71st Annual Meeting Paleontology Society of Vertebrate Las Vegas Paris Nevada, USA Las Vegas, November 2 – 5, 2011 Program and Abstracts Society of Vertebrate Paleontology 71st Annual Meeting Program and Abstracts COMMITTEE MEETING ROOM POSTER SESSION/ CONCURRENT CONCURRENT SESSION EXHIBITS SESSION COMMITTEE MEETING ROOMS AUCTION EVENT REGISTRATION, CONCURRENT MERCHANDISE SESSION LOUNGE, EDUCATION & OUTREACH SPEAKER READY COMMITTEE MEETING POSTER SESSION ROOM ROOM SOCIETY OF VERTEBRATE PALEONTOLOGY ABSTRACTS OF PAPERS SEVENTY-FIRST ANNUAL MEETING PARIS LAS VEGAS HOTEL LAS VEGAS, NV, USA NOVEMBER 2–5, 2011 HOST COMMITTEE Stephen Rowland, Co-Chair; Aubrey Bonde, Co-Chair; Joshua Bonde; David Elliott; Lee Hall; Jerry Harris; Andrew Milner; Eric Roberts EXECUTIVE COMMITTEE Philip Currie, President; Blaire Van Valkenburgh, Past President; Catherine Forster, Vice President; Christopher Bell, Secretary; Ted Vlamis, Treasurer; Julia Clarke, Member at Large; Kristina Curry Rogers, Member at Large; Lars Werdelin, Member at Large SYMPOSIUM CONVENORS Roger B.J. Benson, Richard J. Butler, Nadia B. Fröbisch, Hans C.E. Larsson, Mark A. Loewen, Philip D. Mannion, Jim I. Mead, Eric M. Roberts, Scott D. Sampson, Eric D. Scott, Kathleen Springer PROGRAM COMMITTEE Jonathan Bloch, Co-Chair; Anjali Goswami, Co-Chair; Jason Anderson; Paul Barrett; Brian Beatty; Kerin Claeson; Kristina Curry Rogers; Ted Daeschler; David Evans; David Fox; Nadia B. Fröbisch; Christian Kammerer; Johannes Müller; Emily Rayfield; William Sanders; Bruce Shockey; Mary Silcox; Michelle Stocker; Rebecca Terry November 2011—PROGRAM AND ABSTRACTS 1 Members and Friends of the Society of Vertebrate Paleontology, The Host Committee cordially welcomes you to the 71st Annual Meeting of the Society of Vertebrate Paleontology in Las Vegas. -
A Disease Syndrome in Young Chickens 2-To 8-Weeks - Old Characterized by Erosion and Ulceration of the Gizzard Epithelial Linmg and Black Vomit Has Been Reported
Arch. Insh. Razi, 1981,32, 101-103 A CONDITION OF EROSION AND ULCERATION OF YOUNG CHICKEN'S GIZZARD IN IRAN By: M. Farshian SUMMARY: A disease syndrome in young chickens 2-to 8-weeks - old characterized by erosion and ulceration of the gizzard epithelial linmg and black vomit has been reported. The presence of a dark brown - co!oured fluid in the crop, proventri cul us, gizzard and small intestine was oftenly observed. Tue syndrome caused considerable mortaility losses and reduced weight gain in broilers. INTRODUCTION A few reports from the U.S.A. and Latin Amtrican countries have described a disease syndrome in young chickens known to poultrymen in latter terri tories as « Vomito Negro» or black vomit ( Cover and Paredes, 1971; Johnson and Pinedo; 1971). In Iran a condition very similar to the above mentioned syndrome, coming into being occasionally noticed in the past year or 50, has increased in incidence during the past six months, beginning September 1980. The following is an account of the clinical and gross pathological findings of the syndrome. Clinical signs : Affected chickens, 2-to 8 - weeks - old appeared depressed, lost their appetite and usually had pale combs and wattles. Birds were frequently Wlable to stand and sorne had their necks stretched on the groWld. A dark - coloured diarrhea was not uncommon. Death usually occurred within few hours from the onset of the symptoms. 101 The morbidity rate vearried from 5 % to 25 % and daily mortality ranged from 0.1 % to 1% The disease took a 2-to 3 - week course after which time it appeared that the birds developed sorne sort of resistance to the condition. -
An Important Health and Welfare Issue of Growing Ostriches
DOI: 10.2478/ats-2020-0016 AGRICULTURA TROPICA ET SUBTROPICA, 53/4, 161–173, 2020 Review Article Gastric impaction: an important health and welfare issue of growing ostriches Muhammad Irfan1, Nasir Mukhtar2, Tanveer Ahmad3, Muhammad Tanveer Munir4 1College of Veterinary Medicine, Kyungpook National University, Daegu 41566, Republic of Korea 2Department of Poultry Sciences (Station for Ostrich research & Development), Faculty of Veterinary and Animal Sciences, PMAS‑Arid Agriculture University, Rawalpindi, Pakistan 3Department of Clinical Sciences, Faculty of Veterinary Sciences, Bahauddin Zakariya University, Multan, Pakistan 4LIMBHA, Ecole Supérieur du Bois, 44306 Nantes, France Correspondence to: M. T. Munir, LIMBHA, Ecole Supérieur du Bois, 7 Rue Christian Pauc, 44306 Nantes, France. E‑mail: [email protected] Abstract Ostrich farming serves as a source for meat, feathers, skin, eggs, and oil. In general, ostriches are hardy birds that can resist a wide range of climatic harshness and some diseases. However, musculoskeletal and digestive complications, including the gastric impaction, remain the major cause of mortality. The gastrointestinal impaction alone is responsible for 30 – 46% of spontaneous deaths in growing ostriches. The literature review of 21 publications on this subject has shown that 90% of these incidents happen during first six months of life. The aetiology of this problem is mostly stress and behaviour‑related gorging of feed and picking on non‑feeding materials such as stone, sand, wood pieces, plastic, glass, and metallic objects. Conservative therapy or surgical approaches show good results with almost 70 to 100% recovery depending upon the clinical presentation and timely diagnosis. Overall, this literature review describes impaction in farmed ostriches, along with diagnosis, treatment, and control and preventive measures. -
A Simulated Bird Gastric Mill and Its Implications for Fossil Gastrolith Authenticity
Fossil Record 12 (1) 2009, 91–97 / DOI 10.1002/mmng.200800013 A simulated bird gastric mill and its implications for fossil gastrolith authenticity Oliver Wings Steinmann-Institut fr Geologie, Mineralogie und Palontologie, Universitt Bonn, Nussallee 8, 53115 Bonn, Germany. E-mail: [email protected] Current address: Museum fr Naturkunde Berlin, Invalidenstraße 43, 10115 Berlin, Germany. Abstract Received 12 June 2008 A rock tumbler, stones, water, plant material, hydrochloric acid, and pepsin were used Accepted 15 August 2008 to simulate a bird gizzard in order to study abrasion rate and influence of stomach Published 20 February 2009 juices and foodstuff on gastrolith surface development. The experiment lasted for six months. Each week, the “stomach” was supplied with fresh grass and stomach juices. After the end of the experiment, the set of stones had a combined weight loss of 22.4%, with softer rock types showing higher abrasion rates. The combination of sto- mach juices and silica phytoliths within the grass had no visible effect on stone surface development: polish or pitting did not occur. A second experiment combined only peb- bles with water in the tumbler. Results indicate that rock abrasion is mainly caused by contacts between moving stones. A comparison with authentic ostrich gastroliths Key Words showed that abrasion in the artificial stomach must have been lower than in a real gizzard, but still too high to maintain or develop surface polish. If high polish occa- stomach stones sionally seen on sauropodomorph dinosaur gastroliths was indeed caused in a stomach artificial gizzard environment, it implies digestive processes different from those of extant birds and the clast surface development “artificial gizzard”. -
Convergent Regulatory Evolution and the Origin of Flightlessness in Palaeognathous Birds
bioRxiv preprint doi: https://doi.org/10.1101/262584; this version posted February 8, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Convergent regulatory evolution and the origin of flightlessness in palaeognathous birds Timothy B. Sackton* (1,2), Phil Grayson (2,3), Alison Cloutier (2,3), Zhirui Hu (4), Jun S. Liu (4), Nicole E. Wheeler (5,6), Paul P. Gardner (5,7), Julia A. Clarke (8), Allan J. Baker (9,10), Michele Clamp (1), Scott V. Edwards* (2,3) Affiliations: 1) Informatics Group, Harvard University, Cambridge, USA 2) Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, USA 3) Museum of Comparative Zoology, Harvard University, Cambridge, USA 4) Department of Statistics, Harvard University, Cambridge, USA 5) School of Biological Sciences, University of Canterbury, New Zealand 6) Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK 7) Department of Biochemistry, University of Otago, New Zealand 8) Jackson School of Geosciences, The University of Texas at Austin, Austin, USA 9) Department of Natural History, Royal Ontario Museum, Toronto, Canada 10) Department of Ecology and Evolutionary Biology, University of Toronto, Toronto, Canada *correspondence to: TBS ([email protected]) or SVE ([email protected]) bioRxiv preprint doi: https://doi.org/10.1101/262584; this version posted February 8, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. The relative roles of regulatory and protein evolution in the origin and loss of convergent phenotypic traits is a core question in evolutionary biology. -
Relationships Between Carcass Traits and Offal Components in Local Poultry Populations of Benin Journal of Applied Biosciences 69:5 510 – 5522
Tougan et al . J. Appl. Biosci. 2013 . Relationships between carcass traits and offal components in local poultry populations of Benin Journal of Applied Biosciences 69:5 510 – 5522 ISSN 1997–5902 Relationships between carcass traits and offal components in local poultry populations (gallus gallus ) of Benin Tougan P U 1, Dahouda M 2, Salifou C F A 1, Ahounou G S 1, Kpodekon M T 1, Mensah G A 3, Kossou D N F 1, Amenou C 1, Kogbeto C E 1, Lognay G 4, Thewis 5, Youssao I A K 1 1 Department of Animal Production and Health, Polytechnic School of Abomey-Calavi, 01 BP 2009,Cotonou, Republic of Benin. ² Department of Animal Production, Faculty of Agronomic Science, University of Abomey-Calavi, 01 BP 526, Republic of Benin. 3 Agricultural Research Center of Agonkanmey, National Institute of Agricultural Research of Benin, 01 BP 884, Cotonou 01, Republic of Benin. 4 Laboratory of Analytical Chemistry, Gembloux Agro-Bio Tech, University of Liège, 2, Passage des Déportés -5030 Gembloux, Belgique. 5 Animal Sciences Unit, Gembloux Agro-Bio Tech, University of Liege, Passage des Déportés, 2, 5030 Gembloux, Belgium.. * Correspondence Prof. Issaka YOUSSAO ABDOU KARIM / EPAC / Department of Animal Production and Health, Polytechnic School of Abomey-Calavi, 01 BP 2009,Cotonou, Republic of Benin. Phone : 00 229 95 28 59 88 ou 00 229 97 91 20 74, Fax : 00 229 21 36 01 99. E-mail : [email protected] , [email protected] Original submitted in on 13 th August 2013 Published online at www.m.elewa.org on 30 th September 2013. -
A Giant Ostrich from the Lower Pleistocene Nihewan Formation of North China, with a Review of the Fossil Ostriches of China
diversity Review A Giant Ostrich from the Lower Pleistocene Nihewan Formation of North China, with a Review of the Fossil Ostriches of China Eric Buffetaut 1,2,* and Delphine Angst 3 1 Centre National de la Recherche Scientifique—CNRS (UMR 8538), Laboratoire de Géologie de l’Ecole Normale Supérieure, PSL Research University, 24 rue Lhomond, CEDEX 05, 75231 Paris, France 2 Palaeontological Research and Education Centre, Maha Sarakham University, Maha Sarakham 44150, Thailand 3 School of Earth Sciences, University of Bristol, Life Sciences Building, 24 Tyndall Avenue, Bristol BS8 1TQ, UK; [email protected] * Correspondence: [email protected] Abstract: A large incomplete ostrich femur from the Lower Pleistocene of North China, kept at the Muséum National d’Histoire Naturelle (Paris), is described. It was found by Father Emile Licent in 1925 in the Nihewan Formation (dated at about 1.8 Ma) of Hebei Province. On the basis of the minimum circumference of the shaft, a mass of 300 kg, twice that of a modern ostrich, was obtained. The bone is remarkably robust, more so than the femur of the more recent, Late Pleistocene, Struthio anderssoni from China, and resembles in that regard Pachystruthio Kretzoi, 1954, a genus known from the Lower Pleistocene of Hungary, Georgia and the Crimea, to which the Nihewan specimen is referred, as Pachystruthio indet. This find testifies to the wide geographical distribution Citation: Buffetaut, E.; Angst, D. A of very massive ostriches in the Early Pleistocene of Eurasia. The giant ostrich from Nihewan was Giant Ostrich from the Lower contemporaneous with the early hominins who inhabited that region in the Early Pleistocene. -
The Endangered Kiwi: a Review
REVIEW ARTICLE Folia Zool. – 54(1–2): 1–20 (2005) The endangered kiwi: a review James SALES Bosman street 39, Stellenbosch 7600, South Africa; e-mail: [email protected] Received 13 December 2004; Accepted 1 May 2005 A b s t r a c t . Interest in ratites has necessitated a review of available information on the unique endangered kiwi (Apteryx spp.). Five different species of kiwis, endemic to the three islands of New Zealand, are recognized by the Department of Conservation, New Zealand, according to genetic and biological differences: the North Island Brown Kiwi (Apteryx mantelli), Okarito Brown Kiwi/Rowi (A. rowi), Tokoeka (A. australis), Great Spotted Kiwi/Roroa (A. haastii), and Little Spotted Kiwi (A owenii). As predators were found to be the main reason for declining kiwi numbers, predator control is a main objective of management techniques to prevent kiwis becoming extinct in New Zealand. Further considerations include captive breeding and release, and establishment of kiwi sanctuaries. Body size and bill measurements are different between species and genders within species. Kiwis have the lowest basal rates of metabolism compared with all avian standards. A relative low body temperature (38 ºC), burrowing, a highly developed sense of smell, paired ovaries in females, and a low growth rate, separate kiwis from other avian species. Kiwis have long-term partnerships. Females lay an egg that is approximately 400 % above the allometrically expected value, with an incubation period of 75–85 days. Kiwis mainly feed on soil invertebrate, with the main constituent being earthworms, and are prone to parasites and diseases found in other avian species. -
Gastrointestinal Parasites of a Population of Emus (Dromaius Novaehollandiae) in Brazil S
Brazilian Journal of Biology https://doi.org/10.1590/1519-6984.189922 ISSN 1519-6984 (Print) Original Article ISSN 1678-4375 (Online) Gastrointestinal parasites of a population of emus (Dromaius novaehollandiae) in Brazil S. S. M. Galloa , C. S. Teixeiraa , N. B. Ederlib and F. C. R. Oliveiraa* aLaboratório de Sanidade Animal – LSA, Centro de Ciências e Tecnologias Agropecuárias – CCTA, Universidade Estadual do Norte Fluminense – UENF, CEP 28035-302, Campos dos Goytacazes, RJ, Brasil bInstituto do Noroeste Fluminense de Educação Superior – INFES, Universidade Federal Fluminense – UFF, 28470-000, Santo Antônio de Pádua, RJ, Brasil *e-mail: [email protected] Received: January 9, 2018 – Accepted: June 19, 2018 – Distributed: February 28, 2020 (With 2 figures) Abstract Emus are large flightless birds in the ratite group and are native to Australia. Since the mid-1980s, there has been increased interest in the captive breeding of emus for the production of leather, meat and oil. The aim of this study was to identify gastrointestinal parasites in the feces of emus Dromaius novaehollandiae from a South American scientific breeding. Fecal samples collected from 13 birds were examined by direct smears, both with and without centrifugation, as well as by the fecal flotation technique using Sheather’s sugar solution. Trophozoites, cysts and oocysts of protozoa and nematode eggs were morphologically and morphometrically evaluated. Molecular analysis using PCR assays with specific primers for the genera Entamoeba, Giardia and Cryptosporidium were performed. Trophozoites and cysts of Entamoeba spp. and Giardia spp., oocysts of Eimeria spp. and Isospora dromaii, as well as eggs belonging to the Ascaridida order were found in the feces. -
Phylogeny, Transposable Element and Sex Chromosome Evolution of The
bioRxiv preprint doi: https://doi.org/10.1101/750109; this version posted August 28, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Phylogeny, transposable element and sex chromosome evolution of the basal lineage of birds Zongji Wang1,2,3,* Jilin Zhang4,*, Xiaoman Xu1, Christopher Witt5, Yuan Deng3, Guangji Chen3, Guanliang Meng3, Shaohong Feng3, Tamas Szekely6,7, Guojie Zhang3,8,9,10,#, Qi Zhou1,2,11,# 1. MOE Laboratory of Biosystems Homeostasis & Protection, Life Sciences Institute, Zhejiang University, Hangzhou, 310058, China 2. Department of Molecular Evolution and Development, University of Vienna, Vienna, 1090, Austria 3. BGI-Shenzhen, Beishan Industrial Zone, Shenzhen 518083, China 4. Department of Medical Biochemistry and Biophysics, Karolinska Institutet, SE-171 77, Stockholm, Sweden 5. Department of Biology and the Museum of Southwestern Biology, University of New Mexico, Albuquerque, NM 87131, USA 6. State Key Laboratory of Biocontrol, Department of Ecology, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, China 7. Milner Center for Evolution, Department of Biology and Biochemistry, University of Bath, Bath, BA1 7AY, UK 8 State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China 9. Section for Ecology and Evolution, Department of Biology, University of Copenhagen, DK-2100 Copenhagen, Denmark 10. Center for Excellence in Animal Evolution and Genetics, Chinese Academy of Sciences, Kunming, 650223, China 11. Center for Reproductive Medicine, The 2nd Affiliated Hospital, School of Medicine, Zhejiang University * These authors contributed equally to the work.