Agile Wallaby Survey White Rock Area
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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. -
Ba3444 MAMMAL BOOKLET FINAL.Indd
Intot Obliv i The disappearing native mammals of northern Australia Compiled by James Fitzsimons Sarah Legge Barry Traill John Woinarski Into Oblivion? The disappearing native mammals of northern Australia 1 SUMMARY Since European settlement, the deepest loss of Australian biodiversity has been the spate of extinctions of endemic mammals. Historically, these losses occurred mostly in inland and in temperate parts of the country, and largely between 1890 and 1950. A new wave of extinctions is now threatening Australian mammals, this time in northern Australia. Many mammal species are in sharp decline across the north, even in extensive natural areas managed primarily for conservation. The main evidence of this decline comes consistently from two contrasting sources: robust scientifi c monitoring programs and more broad-scale Indigenous knowledge. The main drivers of the mammal decline in northern Australia include inappropriate fi re regimes (too much fi re) and predation by feral cats. Cane Toads are also implicated, particularly to the recent catastrophic decline of the Northern Quoll. Furthermore, some impacts are due to vegetation changes associated with the pastoral industry. Disease could also be a factor, but to date there is little evidence for or against it. Based on current trends, many native mammals will become extinct in northern Australia in the next 10-20 years, and even the largest and most iconic national parks in northern Australia will lose native mammal species. This problem needs to be solved. The fi rst step towards a solution is to recognise the problem, and this publication seeks to alert the Australian community and decision makers to this urgent issue. -
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. -
Macropus Eugenii J
The effect of pregnancy on the interval between one oestrus and the next in the tammar wallaby, Macropus eugenii J. C. Merchant Division of Wildlife Research, CSIRO, P.O. Box 84, Lyneham, A.C.T. 2602, Australia Summary. In females mated to vasectomized males the interval between oestrous periods was 30\m=.\6\m=+-\1\m=.\17(s.d.) days but when mated to intact males and pregnancy intervened, it was 29\m=.\4\m=+-\1\m=.\26days (P < 0\m=.\025).After removal of pouch young, females carrying diapausing blastocysts gave birth 26\m=.\2days later and came into oestrus 26\m=.\4\m=+-\0\m=.\57(s.d.) days later. When post-partum fertilization was prevented, removal of pouch young was followed by oestrus 30\m=.\4\m=+-\0\m=.\99days later (P < 0\m=.\0005).These results indicate an influence of the conceptus upon the oestrous cycle of Macropus eugenii. Introduction It is well known that the young marsupial exerts a powerful influence on the mother after birth, but in a review of marsupial reproduction Sharman (1970) points out that it has long been thought that it has no effect on the mother before birth and that the placenta has no endocrine function. However, the placenta of the tammar wallaby exerts a morphogenetic effect on the endometrium (Renfree, 1972), possibly as a result of the indirect evidence that the yolk sac placenta of the quokka and the tammar in vitro has the capacity to convert pregnenolone to progesterone (Bradshaw, McDonald, Hahnel & Heller, 1975; Renfree & Heap, 1977). Since gestation in these species is accommodated within the duration of one oestrous cycle it seemed probable that the endocrine function of the placenta is limited to effects on the immediate environment of the uterus but may not affect ovarian events, particularly the life-span of the corpus luteum or the next oestrus and ovulation. -
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 -
Maternal Recognition of Pregnancy in Marsupials
Reviews of Reproduction (2000) 5, 6–11 Maternal recognition of pregnancy in marsupials Marilyn B. Renfree Department of Zoology, University of Melbourne, Parkville, Victoria 3052, Australia Pregnancy in kangaroos and wallabies (macropodid marsupials) induces multiple unilateral responses in the reproductive system that override those related to proximity to the single corpus luteum on one ovary or to the follicle on the contralateral ovary. This situation is in contrast to most other non-macropodid marsupials, in which the responses are dependent on the corpus luteum. There is now good evidence that these unilateral responses in macropodids are controlled by the feto–placental unit acting locally to stimulate the endometrium and myometrium. Pregnancy also influences the duration of the oestrous cycle and maternal be- haviour. The stimuli responsible for these effects probably include paracrine, endocrine and mechanical stimuli resulting from uterine stretch. Taken together, these unilateral responses demonstrate that there is a refined maternal recognition of pregnancy in at least the macro- podid marsupials. The concept of maternal recognition of pregnancy, as described unilateral responses of the pregnant uterus are now well by Short (1969) focused attention on the diverse ways by which defined, particularly for tammar wallabies, which have been the maternal organism first becomes aware of the presence of the subjects of the most detailed studies. an embryo in the uterus. The earliest maternal recognition may occur in the differential tubal -
List of 28 Orders, 129 Families, 598 Genera and 1121 Species in Mammal Images Library 31 December 2013
What the American Society of Mammalogists has in the images library LIST OF 28 ORDERS, 129 FAMILIES, 598 GENERA AND 1121 SPECIES IN MAMMAL IMAGES LIBRARY 31 DECEMBER 2013 AFROSORICIDA (5 genera, 5 species) – golden moles and tenrecs CHRYSOCHLORIDAE - golden moles Chrysospalax villosus - Rough-haired Golden Mole TENRECIDAE - tenrecs 1. Echinops telfairi - Lesser Hedgehog Tenrec 2. Hemicentetes semispinosus – Lowland Streaked Tenrec 3. Microgale dobsoni - Dobson’s Shrew Tenrec 4. Tenrec ecaudatus – Tailless Tenrec ARTIODACTYLA (83 genera, 142 species) – paraxonic (mostly even-toed) ungulates ANTILOCAPRIDAE - pronghorns Antilocapra americana - Pronghorn BOVIDAE (46 genera) - cattle, sheep, goats, and antelopes 1. Addax nasomaculatus - Addax 2. Aepyceros melampus - Impala 3. Alcelaphus buselaphus - Hartebeest 4. Alcelaphus caama – Red Hartebeest 5. Ammotragus lervia - Barbary Sheep 6. Antidorcas marsupialis - Springbok 7. Antilope cervicapra – Blackbuck 8. Beatragus hunter – Hunter’s Hartebeest 9. Bison bison - American Bison 10. Bison bonasus - European Bison 11. Bos frontalis - Gaur 12. Bos javanicus - Banteng 13. Bos taurus -Auroch 14. Boselaphus tragocamelus - Nilgai 15. Bubalus bubalis - Water Buffalo 16. Bubalus depressicornis - Anoa 17. Bubalus quarlesi - Mountain Anoa 18. Budorcas taxicolor - Takin 19. Capra caucasica - Tur 20. Capra falconeri - Markhor 21. Capra hircus - Goat 22. Capra nubiana – Nubian Ibex 23. Capra pyrenaica – Spanish Ibex 24. Capricornis crispus – Japanese Serow 25. Cephalophus jentinki - Jentink's Duiker 26. Cephalophus natalensis – Red Duiker 1 What the American Society of Mammalogists has in the images library 27. Cephalophus niger – Black Duiker 28. Cephalophus rufilatus – Red-flanked Duiker 29. Cephalophus silvicultor - Yellow-backed Duiker 30. Cephalophus zebra - Zebra Duiker 31. Connochaetes gnou - Black Wildebeest 32. Connochaetes taurinus - Blue Wildebeest 33. Damaliscus korrigum – Topi 34. -
Queensland, 2018
Trip report – Queensland, Australia, July 1-21, 2018. I visited Queensland, Australia on a family trip in July. The trip was more family vacation than hard-core mammal watching, and I realize that Queensland is well covered on mammalwatching.com., but I thought I would post a trip report anyway to update some of the information already available. I travelled with my partner, Tracey, and my two children. Josie turned 18 in Australia and Ben is 14. We arrived in Brisbane around noon on July 1. We met up with my niece, Emma, and her partner, Brad, for dinner. The only mammals seen were Homo sapiens, but particularly pleasant and affable specimens. The next day we enjoyed some of Brisbane’s urban delights. That evening we drove to the Greater Glider Conservation Area near Alexandra Hills in Redlands in suburban Brisbane. It’s a fairly small park in suburbia but surprisingly dense with mammals. We saw Greater Glider, Squirrel Glider, about five Common Brushtail Possums and at least six Common Ringtail Possums. Several wallabies were seen which appeared to be Red-necked Wallabies. We then drove out to William Gibbs park. This is an even smaller park next to a school. However we quickly found two Koalas, two Common Ringtail possums and two Grey-headed Flying Foxes. Perhaps they were preparing to enter Noah’s Ark. Anyway, after about four hours we were so tired and jetlagged that we called it a night. Greater Glider The next day we drove to Binna Burra in Lammington National Park, less than two hours from Brisbane. -
Checklist of the Mammals of Western Australia
Records ofthe Western Australian Museum Supplement No. 63: 91-98 (2001). Checklist of the mammals of Western Australia R.A. How, N.K. Cooper and J.L. Bannister Western Australian Museum, Francis Street, Perth, Western Australia 6000, Australia INTRODUCTION continued collection of species across their range. The Checklist ofthe Mammals ofWestern Australia is Where the level of taxonomic uncertainty is being a collation of the most recent systematic information formally resolved, footnotes to the individual taxon on Western Australian mammal taxa, incorporating appear at the end of the family listings. the list of taxa compiled from the Western Numerous taxa have become extinct on a national Australian Museum's mammal database and the or state level since European settlement and there literature. The Checklist presents the nomenclature have been several recent attempts to reintroduce accepted by the Western Australian Museum in regionally extinct taxa to former areas. The present maintaining the state's mammal collection and status of these taxa is indicated by symbols in the database. Listed are those species probably extant Checklist. at the time of arrival of Europeans to Western Australia. Symbols used Nomenclature, in general, follows the Zoological t Denotes extinct taxon. Catalogue ofAustralia, Volume 5, Mammalia (1988). * Denotes taxon extinct in Western Australia but Consideration has been given to the nomenclatural extant in other parts of Australia. decisions in The 1996 Action Plan of Australian $ Denotes taxon extinct on Western Australian Marsupials and Monotremes (Maxwell, Burbidge and mainland and recently reintroduced from other Morris, 1996) and The Action Plan for Australian Bats parts of Australia or translocated from islands (Reardon, 1999a). -
Sarcoptic Mange in Australian Wildlife and It Is Not a Nationally Notifiable Animal Disease
Fact sheet Sarcoptic mange is an infection of the skin in mammals caused by the parasitic mite Sarcoptes scabiei. The parasite can infect both humans and animals, with the disease referred to as scabies and mange respectively. Sarcoptic mange is widely distributed, affecting over 100 species, spanning seven mammalian families. Signs of mange include intense scratching, skin reddening, skin thickening and hair loss. Severity of the infection and mortality rates vary depending on species and geographic location. The mite is invasive to Australia and is believed to have arrived about 200 years ago with European settlers and their domesticated animals. Since its introduction, S. scabiei has been documented in a number of native Australian species. Sarcoptic manage can have significant health and welfare impacts on individual animals and can result in the death of affected individuals. Sarcoptic mange has the most significant impacts on wombat populations and can cause local extirpation of populations. Increased management and population scale treatments may be required to protect isolated or small wombat populations. Mange is caused by the sub-macroscopic (200-500 m in length), obligate parasitic mite, Sarcoptes scabiei (Family Sarcoptidae) (Bornstein et al. 2001; Pence and Ueckermann 2002). The burrowing mite creates tunnels in the epidermis, as deep as the stratum germinativum, where adult mites, eggs, larvae, and nymphs can be found. In these tunnels, the mites consume the host’s living cells and fluids. Sarcoptes scabiei infects a variety of different mammalian hosts, and while mites that originate in different host species are morphologically indistinguishable in most cases, they do exhibit a degree of host specificity (Bornstein et al. -
Agile Wallaby
Husbandry Guidelines for Agile Wallaby Macropus agilis Mammalia: (Macropodidae) Author: Ms. Shayne Sadler Date of Preparation: July 2009-November 2010 Western Sydney Institute of TAFE, Richmond Course Name and Number: Certificate 3 Captive Animals Lecturer: Graeme Phipps, Jackie Salkeld, Brad Walker, 1 DISCLAIMER 2 OCCUPATIONAL HEALTH AND SAFETY RISKS. Human salmonellosis is one of the most common and economically important zoonotic diseases in the world. It is therefore important to recognize that macropods can harbour salmonellae without displaying clinical signs of disease. Macropods held in captivity and hand reared joeys are particularly susceptible to infection. (Spear & Thomas 1988). Studies have also demonstrated the presence of infection in a large number of healthy, captive macropods. These animals may have become infected as a result of oral consumption of contaminated feed or water. (Samuel 1982). Minimising diet and environmental related stress is paramount in preventing and controlling Salmonella in macropods in captivity and joeys in care. It is therefore important for ALL individuals coming into contact with these animals to practise high standards of hygiene at all times. Care must be taken in working with Macropods. If a large joey or wallaby has to be caught, it can be a dangerous task; the preferred method is to grab its tail close to the rump, and pass your other arm under its forearms across the front of the ribs – BE CAREFUL some will and do bite and scratch. Refer to Section 7 about specific capture and handling techniques. Do Not underestimate a macropods’ kick – many injuries can be sustained by incorrect restraint/capture methods. -
Sarcoptic Mange in Australian Wildlife May 2017
Sarcoptic mange in Australian wildlife Fact sheet Introductory statement Sarcoptic mange is an infection of the skin in mammals caused by the parasitic mite Sarcoptes scabiei. The parasite can infect both humans and wildlife, with the disease referred to as scabies and mange respectively. Sarcoptic mange is widely distributed, affecting over 100 species, spanning seven mammalian families. Signs of mange include intense scratching, skin reddening, skin thickening and hair loss. Severity of the infection and mortality rates vary depending on species and geographic location. The mite is invasive to Australia and is believed to have arrived about 200 years ago with European settlers and their domesticated animals. Since its introduction, S. scabiei has been documented in a number of native Australian species. Sarcoptic mange has the most significant impacts on wombat populations and can cause local extirpation of populations. Increased management and population scale treatments may be required to protect isolated or small wombat populations. Aetiology Mange is caused by the sub-macroscopic (200-500 m in length), obligate parasitic mite, Sarcoptes scabiei (Family Sarcoptidae) (Bornstein et al. 2001; Pence and Ueckermann 2002). The burrowing mite creates tunnels in the epidermis, as deep as the stratum germinativum, where adult mites, eggs, larvae, and nymphs can be found. In these tunnels, the mites consume the host’s living cells and fluids. Sarcoptes scabiei infects a variety of different mammalian hosts, and while mites that originate in different host species are morphologically indistinguishable in most cases, they do exhibit a degree of host specificity (Bornstein et al. 2001). The different strains, or varieties, of the mite represent a single, highly diverse species.