A Natural Grey Kangaroo Hybrid?
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New Operational Taxonomic Units of Enterocytozoon in Three Marsupial Species Yan Zhang1, Anson V
Zhang et al. Parasites & Vectors (2018) 11:371 https://doi.org/10.1186/s13071-018-2954-x RESEARCH Open Access New operational taxonomic units of Enterocytozoon in three marsupial species Yan Zhang1, Anson V. Koehler1* , Tao Wang1, Shane R. Haydon2 and Robin B. Gasser1* Abstract Background: Enterocytozoon bieneusi is a microsporidian, commonly found in animals, including humans, in various countries. However, there is scant information about this microorganism in Australasia. In the present study, we conducted the first molecular epidemiological investigation of E. bieneusi in three species of marsupials (Macropus giganteus, Vombatus ursinus and Wallabia bicolor) living in the catchment regions which supply the city of Melbourne with drinking water. Methods: Genomic DNAs were extracted from 1365 individual faecal deposits from these marsupials, including common wombat (n = 315), eastern grey kangaroo (n = 647) and swamp wallaby (n = 403) from 11 catchment areas, and then individually tested using a nested PCR-based sequencing approach employing the internal transcribed spacer (ITS) and small subunit (SSU) of nuclear ribosomal DNA as genetic markers. Results: Enterocytozoon bieneusi was detected in 19 of the 1365 faecal samples (1.39%) from wombat (n =1), kangaroos (n = 13) and wallabies (n =5).TheanalysisofITS sequence data revealed a known (designated NCF2) and four new (MWC_m1 to MWC_m4) genotypes of E. bieneusi. Phylogenetic analysis of ITS sequence data sets showed that MWC_m1 (from wombat) clustered with NCF2, whereas genotypes MWC_m2 (kangaroo and wallaby), MWC_m3 (wallaby) and MWC_m4 (kangaroo) formed a new, divergent clade. Phylogenetic analysis of SSU sequence data revealed that genotypes MWC_m3 and MWC_m4 formed a clade that was distinct from E. -
Platypus Collins, L.R
AUSTRALIAN MAMMALS BIOLOGY AND CAPTIVE MANAGEMENT Stephen Jackson © CSIRO 2003 All rights reserved. Except under the conditions described in the Australian Copyright Act 1968 and subsequent amendments, no part of this publication may be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, mechanical, photocopying, recording, duplicating or otherwise, without the prior permission of the copyright owner. Contact CSIRO PUBLISHING for all permission requests. National Library of Australia Cataloguing-in-Publication entry Jackson, Stephen M. Australian mammals: Biology and captive management Bibliography. ISBN 0 643 06635 7. 1. Mammals – Australia. 2. Captive mammals. I. Title. 599.0994 Available from CSIRO PUBLISHING 150 Oxford Street (PO Box 1139) Collingwood VIC 3066 Australia Telephone: +61 3 9662 7666 Local call: 1300 788 000 (Australia only) Fax: +61 3 9662 7555 Email: [email protected] Web site: www.publish.csiro.au Cover photos courtesy Stephen Jackson, Esther Beaton and Nick Alexander Set in Minion and Optima Cover and text design by James Kelly Typeset by Desktop Concepts Pty Ltd Printed in Australia by Ligare REFERENCES reserved. Chapter 1 – Platypus Collins, L.R. (1973) Monotremes and Marsupials: A Reference for Zoological Institutions. Smithsonian Institution Press, rights Austin, M.A. (1997) A Practical Guide to the Successful Washington. All Handrearing of Tasmanian Marsupials. Regal Publications, Collins, G.H., Whittington, R.J. & Canfield, P.J. (1986) Melbourne. Theileria ornithorhynchi Mackerras, 1959 in the platypus, 2003. Beaven, M. (1997) Hand rearing of a juvenile platypus. Ornithorhynchus anatinus (Shaw). Journal of Wildlife Proceedings of the ASZK/ARAZPA Conference. 16–20 March. -
Post-Release Monitoring of Western Grey Kangaroos (Macropus Fuliginosus) Relocated from an Urban Development Site
animals Article Post-Release Monitoring of Western Grey Kangaroos (Macropus fuliginosus) Relocated from an Urban Development Site Mark Cowan 1,* , Mark Blythman 1, John Angus 1 and Lesley Gibson 2 1 Biodiversity and Conservation Science, Department of Biodiversity, Conservation and Attractions, Wildlife Research Centre, Woodvale, WA 6026, Australia; [email protected] (M.B.); [email protected] (J.A.) 2 Biodiversity and Conservation Science, Department of Biodiversity, Conservation and Attractions, Kensington, WA 6151, Australia; [email protected] * Correspondence: [email protected]; Tel.: +61-8-9405-5141 Received: 31 August 2020; Accepted: 5 October 2020; Published: 19 October 2020 Simple Summary: As a result of urban development, 122 western grey kangaroos (Macropus fuliginosus) were relocated from the outskirts of Perth, Western Australia, to a nearby forest. Tracking collars were fitted to 67 of the kangaroos to monitor survival rates and movement patterns over 12 months. Spotlighting and camera traps were used as a secondary monitoring technique particularly for those kangaroos without collars. The survival rate of kangaroos was poor, with an estimated 80% dying within the first month following relocation and only six collared kangaroos surviving for up to 12 months. This result implicates stress associated with the capture, handling, and transport of animals as the likely cause. The unexpected rapid rate of mortality emphasises the importance of minimising stress when undertaking animal relocations. Abstract: The expansion of urban areas and associated clearing of habitat can have severe consequences for native wildlife. One option for managing wildlife in these situations is to relocate them. -
Exotic to Australia
Fact sheet Introductory statement Foot and mouth disease (FMD) is a highly contagious viral vesicular disease of cloven hoofed animals. It is a major issue in international trade in livestock and livestock products. Australia is free of the disease and it is vital that it remains so. The 2001 outbreak in the United Kingdom resulted in over 10 million cattle and sheep being slaughtered at a cost of over GBP 8 billion in order to eradicate the disease. This fact sheet summarises what is known about FMD and Australian native wildlife. WHA also manages an fact sheet that briefly summarises information on FMD and feral animals “Foot and Mouth Disease (General Information)”. Aetiology and natural hosts FMD is caused by an aphthovirus belonging to the family Picornaviridae. It is a single stranded non enveloped 25 nm RNA virus. There are seven serotypes: A, O, C, SAT 1, SAT 2, SAT 3, and Asia 1. All cloven hoofed animals are considered susceptible. Cases have also been reported in elephants, hedgehogs and some rodents. World distribution and occurrences in Australia FMD is endemic in Africa, the Middle East, Asia and parts of South America. The disease has almost been eradicated from Europe with the most recent cases occurring in the United Kingdom and Cyprus in 2007. FMD has not occurred in Australia for over 130 years, and then only in livestock. Minor outbreaks occurred in 1801, 1804, 1871 and 1872 (Geering et al 1995). However, a case was reported in an eastern grey kangaroo (Macropus giganteus) held in a zoo in India (Bhattacharya et al 2003). -
The Kangaroo Island Tammar Wallaby
The Kangaroo Island Tammar Wallaby Assessing ecologically sustainable commercial harvesting A report for the Rural Industries Research and Development Corporation by Margaret Wright and Phillip Stott University of Adelaide March 1999 RIRDC Publication No 98/114 RIRDC Project No. UA-40A © 1999 Rural Industries Research and Development Corporation. All rights reserved. ISBN 0 642 57879 6 ISSN 1440-6845 "The Kangaroo Island Tammar Wallaby - Assessing ecologically sustainable commercial harvesting " Publication No: 98/114 Project No: UA-40A The views expressed and the conclusions reached in this publication are those of the author and not necessarily those of persons consulted. RIRDC shall not be responsible in any way whatsoever to any person who relies in whole or in part on the contents of this report. This publication is copyright. However, RIRDC encourages wide dissemination of its research, providing the Corporation is clearly acknowledged. For any other enquiries concerning reproduction, contact the Publications Manager on phone 02 6272 3186. Researcher Contact Details Margaret Wright & Philip Stott Department of Environmental Science and Management University of Adelaide ROSEWORTHY SA 5371 Phone: 08 8303 7838 Fax: 08 8303 7956 Email: [email protected] [email protected] Website: http://www.roseworthy.adelaide.edu.au/ESM/ RIRDC Contact Details Rural Industries Research and Development Corporation Level 1, AMA House 42 Macquarie Street BARTON ACT 2600 PO Box 4776 KINGSTON ACT 2604 Phone: 02 6272 4539 Fax: 02 6272 5877 Email: [email protected] Website: http://www.rirdc.gov.au Published in March 1999 Printed on environmentally friendly paper by Canprint ii Foreword The Tammar Wallaby on Kangaroo Island, South Australia, is currently managed as a vertebrate pest. -
Eastern Grey Kangaroo Macropus Giganteus Shaw 1790 As a Vulnerable Species in Part 1 of Schedule 2 of the Act
NSW SCIENTIFIC COMMITTEE Preliminary Determination The Scientific Committee, established by the Threatened Species Conservation Act, has made a Preliminary Determination NOT to support a proposal to list the Eastern Grey Kangaroo Macropus giganteus Shaw 1790 as a Vulnerable species in Part 1 of Schedule 2 of the Act. Rejection of nominations is provided for by Part 2 of the Act. The Scientific Committee has found that: 1. Macropus giganteus Shaw 1790 (family Macropodidae), known as the Eastern Grey Kangaroo, is a large, highly sexually dimorphic macropod. Head-body to 2302 mm (males), 1857 mm (females); tail to 1090 mm (males), 842 mm (females); weight to 85 kg (males), 42 kg (females). Grey-brown dorsally, paler ventrally and on legs. Ears long, dark brown outside, pale grey inside with whitish fringe. Distal third of tail blackish. Muzzle finely haired (Menkhorst and Knight 2001; Johnson 2006; Coulson 2008). 2. Macropus giganteus is endemic to Australia. It is widely distributed in eastern Australia from Cape York Peninsula, Queensland, to far southeast South Australia and northeastern Tasmania. It is found throughout New South Wales (NSW). In western NSW, northwestern Victoria and southwestern Queensland M. giganteus is sympatric with its sister species the Western Grey Kangaroo (Macropus fuliginosus) (Johnson 2006; Coulson 2008). Eastern and Western Grey Kangaroos were recognised as separate species only in the 1970s (Kirsch and Poole 1972). Macropus giganteus mostly occurs where annual rainfall is >250 mm (Caughley et al. 1987b) in sclerophyll forest, woodland (including mallee), shrubland and heathland. It can also occur in modified habitats including farmland with remnant native vegetation, pine plantations and golf courses (Menkhorst and Knight 2001; Johnson 2006; Coulson 2008; Dawson 2012). -
Improving Reliability of Scat Counts for Abundance and Distribution Estimations of Lumholtz’S Tree-Kangaroo (Dendrolagus Lumholtzi) in Its Rainforest Habitats
Improving reliability of scat counts for abundance and distribution estimations of Lumholtz’s Tree-kangaroo (Dendrolagus lumholtzi) in its rainforest habitats SIGRID R. HEISE-PAVLOV1 and RHIANA D. MEADE2 Non-invasive methods are essential in the study of cryptic species. For estimations on abundances and distributions of arboreal folivores, such as Lumholtz’s Tree-kangaroo (Dendrolagus lumholtzi) in Far North Queensland, Australia, scat counts seem to be the most promising ecological technique. However, the occurrence of Lumholtz’s Tree-kangaroos in seasonal rainforests with dense understory, a high diversity of coprophagous invertebrates and with sympatric folivores increases the probability of invalidating results based on scat surveys. This study investigates scat production and scat decomposition patterns to select diagnostic traits of Lumholtz’s Tree-kangaroo scats that can, under varying environmental conditions, assist in distinguishing between fresh and old scats to reduce false positive and false negative errors in species presence due to non- or/and misidentification of scats. Scat production rates of six captive Lumholtz’s Tree-kangaroos were highly variable resulting in different scat numbers and masses. Changes in scat size (mass and circumference), pH and the appearance of mould were monitored under different laboratory conditions and in forest trials. Under wet conditions scats gained mass until they reached an apparent plateau of 130% of their original mass. Scats under dry conditions lost up to 90% of their original mass. Changes in mass were accompanied by changes in circumference of scats. By Day 3 scats had developed signs of mould under laboratory conditions and showed an acidic pH. Field trials revealed a high loss of scats due primarily to their consumption by dung beetles (Scarabaeoidea). -
Mammals of the Avon Region
Mammals of the Avon Region By Mandy Bamford, Rowan Inglis and Katie Watson Foreword by Dr. Tony Friend R N V E M E O N G T E O H F T W A E I S L T A E R R N A U S T 1 2 Contents Foreword 6 Introduction 8 Fauna conservation rankings 25 Species name Common name Family Status Page Tachyglossus aculeatus Short-beaked echidna Tachyglossidae not listed 28 Dasyurus geoffroii Chuditch Dasyuridae vulnerable 30 Phascogale calura Red-tailed phascogale Dasyuridae endangered 32 phascogale tapoatafa Brush-tailed phascogale Dasyuridae vulnerable 34 Ningaui yvonnae Southern ningaui Dasyuridae not listed 36 Antechinomys laniger Kultarr Dasyuridae not listed 38 Sminthopsis crassicaudata Fat-tailed dunnart Dasyuridae not listed 40 Sminthopsis dolichura Little long-tailed dunnart Dasyuridae not listed 42 Sminthopsis gilberti Gilbert’s dunnart Dasyuridae not listed 44 Sminthopsis granulipes White-tailed dunnart Dasyuridae not listed 46 Myrmecobius fasciatus Numbat Myrmecobiidae vulnerable 48 Chaeropus ecaudatus Pig-footed bandicoot Peramelinae presumed extinct 50 Isoodon obesulus Quenda Peramelinae priority 5 52 Species name Common name Family Status Page Perameles bougainville Western-barred bandicoot Peramelinae endangered 54 Macrotis lagotis Bilby Peramelinae vulnerable 56 Cercartetus concinnus Western pygmy possum Burramyidae not listed 58 Tarsipes rostratus Honey possum Tarsipedoidea not listed 60 Trichosurus vulpecula Common brushtail possum Phalangeridae not listed 62 Bettongia lesueur Burrowing bettong Potoroidae vulnerable 64 Potorous platyops Broad-faced -
Blastocystis in Australian Wildlife Jul 2011
Blastocystis in Australian wildlife Fact sheet Introductory statement Blastocystis is a protozoan parasite which infects a wide variety of hosts including humans and other mammals, birds, reptiles and amphibians (Tan 2004). This parasite is known to cause intestinal disease in humans and non human primates. Recent research has identified Blastocystis in some species of Australian wildlife but pathogenicity remains undetermined. Aetiology Blastocystosis is caused by the protozoan Blastocystis sp. Infection may result in gastrointestinal disease in the host. The taxonomy of Blastocystis has often changed due to the unique morphology and cellular components. Molecular characterisation has suggested this protist belongs in the group (Stramenopiles), genus Blastocystis. Natural hosts Blastocystis sp. are known to infect a wide variety of vertebrate hosts including humans, non-human primates, companion animals, livestock, birds, amphibians and reptiles. World distribution Occurs throughout the world. Occurrences in Australia There are few reports of Blastocystis sp. within Australian wildlife most likely due to the difficultly in identifying infection through direct microscopy as cysts can be confused with yeast and faecal debris. However, a recent study using molecular techniques has identified this parasite in the chuditch (Dasyurus geoffroii), brushtail possum (Trichuris vulpecular), quenda (Isoodon obesulus) and woylie (Bettongia penicillata) (Parkar et al. 2007). It has also been observed in captive populations of the western grey kangaroo (Macropus fuliginosus), quokka (Setonix brachyurous) and southern hairy nosed wombat (Lasiorhinus latifrons) (Parkar et al. 2010). Epidemiology Blastocystis is predominantly transmitted directly through the faecal-oral route however the water resistant cysts can also be transmitted indirectly through contaminated water sources (Tan 2004). -
On the Evolution of Kangaroos and Their Kin (Family Macropodidae) Using Retrotransposons, Nuclear Genes and Whole Mitochondrial Genomes
ON THE EVOLUTION OF KANGAROOS AND THEIR KIN (FAMILY MACROPODIDAE) USING RETROTRANSPOSONS, NUCLEAR GENES AND WHOLE MITOCHONDRIAL GENOMES William George Dodt B.Sc. (Biochemistry), B.Sc. Hons (Molecular Biology) Principal Supervisor: Dr Matthew J Phillips (EEBS, QUT) Associate Supervisor: Dr Peter Prentis (EEBS, QUT) External Supervisor: Dr Maria Nilsson-Janke (Senckenberg Biodiversity and Research Centre, Frankfurt am Main) Submitted in fulfilment of the requirements for the degree of Doctor of Philosophy Science and Engineering Faculty Queensland University of Technology 2018 1 Keywords Adaptive radiation, ancestral state reconstruction, Australasia, Bayesian inference, endogenous retrovirus, evolution, hybridization, incomplete lineage sorting, incongruence, introgression, kangaroo, Macropodidae, Macropus, mammal, marsupial, maximum likelihood, maximum parsimony, molecular dating, phylogenetics, retrotransposon, speciation, systematics, transposable element 2 Abstract The family Macropodidae contains the kangaroos, wallaroos, wallabies and several closely related taxa that occupy a wide variety of habitats in Australia, New Guinea and surrounding islands. This group of marsupials is the most species rich family within the marsupial order Diprotodontia. Despite significant investigation from previous studies, much of the evolutionary history of macropodids (including their origin within Diprotodontia) has remained unclear, in part due to an incomplete early fossil record. I have utilized several forms of molecular sequence data to shed -
Behaviour, Group Dynamics, and Health of Free-Ranging Eastern Grey Kangaroos
Behaviour, group dynamics, and health of free-ranging eastern grey kangaroos (Macropus giganteus) Jai Mikaela Green-Barber Submitted for the completion of a Doctor of Philosophy (Science) degree at Western Sydney University November 2017 Dedication The following thesis is dedicated to my hero. You instilled in me an appreciation of nature and of knowledge, you showed me the joys of solving puzzles and debating ideas, and you always encouraged me to be daring when the reward was worth the risk. Most importantly you always taught me to laugh along the way, to laugh at myself, and not take life too seriously. These gifts you have given me have led me down this path, and gave me the strength to complete the journey. Your influence will continue to shape the rest of my life. This one’s for you Dad xoxo Acknowledgements I would like to thank Associate Professor Julie Old for the encouragement and support needed to complete this thesis. I really appreciate you putting up with my essay length emails full of questions and all the feedback on the countless draft manuscripts and presentations produced throughout my candidature. To Dr Hayley Stannard, thank you for teaching me to collect blood samples and run blood chemistry analysis, and for the helpful feedback on draft manuscripts. Thank you to Dr Oselyne Ong for teaching me how to run antimicrobial assays, Megan Callander for teaching me how to use various microsatellite analysis software, and Professor John Hunt for providing feedback on draft manuscripts and advice on analysis. To all the volunteers that assisted me in the field your help was greatly appreciated. -
Disclosure Document F0001488301
Numbers of permits granted by the Department for the destruction of wildlife issued for each animal under the National Parks and Wildlife Act 1972 for the period 1 July 2016 to 30 June 2017 AND Numbers of animals allowed to be killed AND the reasons for the permits being issued Table 1: Number of permits granted under the National Parks and Wildlife Act 1972 for the destruction of wildlife Financial year Number of permits granted 1 July 2016 to 30 June 2017 1008 Table 2: Summary of Permits to Destroy Wildlife by species for the period 1 July 2016 to 30 June 2017 Species Permits that include No. of animals this species issued on Permit Adelaide Rosella 45 3241 Australian Hobby 2 # Australian Magpie 6 42 Australian Pelican 2 # Australian Pratincole 2 # Australian Raven 1 # Australian Shelduck 4 32 Australian White Ibis 5 56 Australian Wood Duck (Maned Duck) 30 927 Banded Lapwing 2 # Barn Owl 2 # Black Kite 2 70 Black Swan 4 36 Black-faced Cormorant 1 125 Black-fronted Dotterel 1 # Black-shouldered Kite 2 # Black-tailed Native Hen 2 # Brown Falcon 2 # Brown Goshawk 2 # Brown Songlark 2 # Cape Barren Goose 15 241 Common Brushtail Possum 57 6420 Crested Pigeon 2 # Eastern Grey Kangaroo 28 1610 Emu 118 2810 Euro 100 3262 Fairy Martin 2 # Galah 2 # Gould's Wattled Bat 1 # Grey Teal, (Australasian Teal) 1 # Hardhead (White-eyed Duck) 1 # Little Corella 2 # Little Pied Cormorant 1 # Page 1 of 4 Document released by DEWNR under the Freedom of Information Act 1991 1 of 4 Numbers of permits granted by the Department for the destruction of wildlife issued for each animal under the National Parks and Wildlife Act 1972 for the period 1 July 2016 to 30 June 2017 AND Numbers of animals allowed to be killed AND the reasons for the permits being issued Species Permits that include No.