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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. -
Feral Cats: Killing 75 Million Native Animals Every Night Saving Australia’S Threatened Wildlife
wildlife matters Summer 2012/13 Feral cats: killing 75 million native animals every night Saving Australia’s threatened wildlife Welcome to the Summer 2012/13 edition of Wildlife Matters. The AWC mission As you will read in the following pages, our focus remains firmly on battling the The mission of Australian Wildlife “ecological axis of evil” – feral animals, wildfires and weeds. For decades, these Conservancy (AWC) is the effective forces have been steadily eroding Australia’s natural capital, causing the extinction conservation of all Australian animal of wildlife and the destruction of habitats and ecological processes. The role of feral species and the habitats in which they live. cats – which kill 75 million native animals every day – is particularly significant. To achieve this mission, our actions are focused on: Our response to this tripartite attack on Australia’s natural capital is straightforward • Establishing a network of sanctuaries – we deliver practical land management informed by world-class science. Central which protect threatened wildlife and to our strategy is the fact that around 80% of our staff are based in the field. AWC’s ecosystems: AWC now manages dedicated team of field operatives – land managers and ecologists – represent the 23 sanctuaries covering over 3 million front-line in our battle against fire, ferals and weeds. Within the conservation sector, hectares (7.4 million acres). we are unique in deploying such a high proportion of our staff in the field. • Implementing practical, on-ground To date, this strategy has delivered significant, measurable and very positive conservation programs to protect ecological returns. This success is particularly apparent when considering the the wildlife at our sanctuaries: these surviving populations of Australia’s most endangered mammals. -
Phascogale Calura) Corinne Letendre, Ethan Sawyer, Lauren J
Letendre et al. BMC Zoology (2018) 3:10 https://doi.org/10.1186/s40850-018-0036-3 BMC Zoology RESEARCHARTICLE Open Access Immunosenescence in a captive semelparous marsupial, the red-tailed phascogale (Phascogale calura) Corinne Letendre, Ethan Sawyer, Lauren J. Young and Julie M. Old* Abstract Background: The red-tailed phascogale is a ‘Near Threatened’ dasyurid marsupial. Males are semelparous and die off shortly after the breeding season in the wild due to a stress-related syndrome, which has many physiological and immunological repercussions. In captivity, males survive for more than 2 years but become infertile after their first breeding season. Meanwhile, females can breed for many years. This suggests that captive males develop similar endocrine changes as their wild counterparts and undergo accelerated aging. However, this remains to be confirmed. The health status and immune function of this species in captivity have also yet to be characterized. Results: Through an integrative approach combining post-mortem examinations, blood biochemical and hematological analyses, we investigated the physiological and health status of captive phascogales before, during, and after the breeding season. Adult males showed only mild lesions compatible with an endocrine disorder. Both sexes globally maintained a good body condition throughout their lives, most likely due to a high quality diet. However, biochemistry changes potentially compatible with an early onset of renal or hepatic insufficiency were detected in older individuals. Masses and possible hypocalcemia were observed anecdotally in old females. With this increased knowledge of the physiological status of captive phascogales, interpretation of their immune profile at different age stages was then attempted. -
Cercartetus Concinnus Western Pygmy-Possum
MAMMAL Cercartetus concinnus Western Pygmy-possum AUS SA AMLR Endemism Residency Adelaide region.7 - - V - Resident Post-1983 AMLR filtered records confined to Cleland CP, Cox Scrub CP, Scott CP, Mount Billy CP, Mount Magnificent CP, and vegetation blocks under Heritage Agreement around Inman Valley and Newland Head CP.3 One pre-1983 AMLR filtered record, near Inman Valley.3 Also recorded from near Mount Barker (1957) and Reynella (1945).1 Habitat Found in mallee heath and dry sclerophyll forest, especially where there is an undergrowth of shrubs such as Banksias, Grevilleas, Callistemons and Melaleucas. In mallee and woodland restricted to shrubby areas.1,6 Photo: © Julia Bignall Conservation Significance Mainly arboreal and nocturnal (Smith 1995). During the The AMLR distribution is disjunct, isolated from other day rests in hollows or among the leaves of 2 extant occurrences within SA. Within the AMLR the Xanthorrhoea spp. (Smith 1995). species’ relative area of occupancy is classified as ‘Extremely Restricted’. Relative to all AMLR extant Within the AMLR the preferred broad vegetation 3 species, the species' taxonomic uniqueness is groups are Mallee and Heathy Woodland. classified as ‘Very High’.3 Biology and Ecology Description Young are born in most months. Some reproductively Small nocturnal marsupial, fawn or reddish-brown active males are probably present at all times of the above, white below and a finely-scaled, naked tail.6 year. Females can rear two or three litters in close 8 Adults on average weigh 13 g. Adapted for climbing succession. and forages at night both on the ground and in shrubs and trees (Smith 1995). -
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. -
What Role Does Ecological Research Play in Managing Biodiversity in Protected Areas? Australia’S Oldest National Park As a Case Study
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by The University of Sydney: Sydney eScholarship Journals online What Role Does Ecological Research Play in Managing Biodiversity in Protected Areas? Australia’s Oldest National Park as a Case Study ROSS L. GOLDINGAY School of Environmental Science & Management, Southern Cross University, Lismore, NSW 2480 Published on 3 September 2012 at http://escholarship.library.usyd.edu.au/journals/index.php/LIN Goldingay, R.L. (2012). What role does ecological research play in managing biodiversity in protected areas? Australia’s oldest National Park as a case study. Proceedings of the Linnean Society of New South Wales 134, B119-B134. How we manage National Parks (protected areas or reserves) for their biodiversity is an issue of current debate. At the centre of this issue is the role of ecological research and its ability to guide reserve management. One may assume that ecological science has suffi cient theory and empirical evidence to offer a prescription of how reserves should be managed. I use Royal National Park (Royal NP) as a case study to examine how ecological science should be used to inform biodiversity conservation. Ecological research relating to reserve management can be: i) of generic application to reserve management, ii) specifi c to the reserve in which it is conducted, and iii) conducted elsewhere but be of relevance due to the circumstances (e.g. species) of another reserve. I outline how such research can be used to inform management actions within Royal NP. I also highlight three big challenges for biodiversity management in Royal NP: i) habitat connectivity, ii) habitat degradation and iii) fi re management. -
An Assessment of the Non-Volant Mammal
AN ASSESSMENT OF THE NON-VOLANT 1 MAMMAL FAUNA OF THE AREA BETWEEN DAWESVILLE AND BINNINGUP, SOUTHERN SWAN COASTAL PLAIN Western Grey Kangaroo – Photo: B Hyder Report prepared for: Environmental Protection Authority October 2009 Bridget Hyder and John Dell, Department of Environment and Conservation 1 This report only covers non-flying mammals; bats are included in a separate report (Bullen 2009) INTRODUCTION The Western Australia Museum (How 1978) documented the vertebrate and aquatic fauna of the northern Swan Coastal Plain between the Swan and Moore Rivers and evaluated the impact of the first 150 years of European settlement on the indigenous fauna. That study concluded that the impact of settlement had been most pronounced on the mammalian fauna. Reviewing all available data, How and Dell (1993) later stated that at the time of European settlement 16 species of non-volant (non-flying) native mammals were known from the Swan Coastal Plain and many of these species had subsequently decreased in abundance and distribution. The status of many of these species is continuing to decline as a direct result of vegetation clearing and some of these species are now absent from many parts of the Swan Coastal Plain where habitat loss and modification has been most severe. The Museum survey documented mammals of the northern Swan Coastal Plain. However, in comparison little information is currently available on the status of mammals on the southern Swan Coastal Plain. The purpose of this report is to examine the current status of non-volant mammals on that part of the southern Swan Coastal Plain from Dawesville to the Leschenault Estuary, hereafter called the Dawesville to Binningup study area. -
Cercartetus Lepidus (Diprotodontia: Burramyidae)
MAMMALIAN SPECIES 842:1–8 Cercartetus lepidus (Diprotodontia: Burramyidae) JAMIE M. HARRIS School of Environmental Science and Management, Southern Cross University, Lismore, New South Wales, 2480, Australia; [email protected] Abstract: Cercartetus lepidus (Thomas, 1888) is a burramyid commonly called the little pygmy-possum. It is 1 of 4 species in the genus Cercartetus, which together with Burramys parvus form the marsupial family Burramyidae. This Lilliputian possum has a disjunct distribution, occurring on mainland Australia, Kangaroo Island, and in Tasmania. Mallee and heath communities are occupied in Victoria and South Australia, but in Tasmania it is found mainly in dry and wet sclerophyll forests. It is known from at least 18 fossil sites and the distribution of these reveal a significant contraction in geographic range since the late Pleistocene. Currently, this species is not listed as threatened in any state jurisdictions in Australia, but monitoring is required in order to more accurately define its conservation status. DOI: 10.1644/842.1. Key words: Australia, burramyid, hibernator, little pygmy-possum, pygmy-possum, Tasmania, Victoria mallee Published 25 September 2009 by the American Society of Mammalogists Synonymy completed 2 April 2008 www.mammalogy.org Cercartetus lepidus (Thomas, 1888) Little Pygmy-possum Dromicia lepida Thomas, 1888:142. Type locality ‘‘Tasma- nia.’’ E[udromicia](Dromiciola) lepida: Matschie, 1916:260. Name combination. Eudromicia lepida Iredale and Troughton, 1934:23. Type locality ‘‘Tasmania.’’ Cercartetus lepidus: Wakefield, 1963:99. First use of current name combination. CONTEXT AND CONTENT. Order Diprotodontia, suborder Phalangiformes, superfamily Phalangeroidea, family Burra- myidae (Kirsch 1968). No subspecies for Cercartetus lepidus are currently recognized. -
A Preliminary Risk Assessment of Cane Toads in Kakadu National Park Scientist Report 164, Supervising Scientist, Darwin NT
supervising scientist 164 report A preliminary risk assessment of cane toads in Kakadu National Park RA van Dam, DJ Walden & GW Begg supervising scientist national centre for tropical wetland research This report has been prepared by staff of the Environmental Research Institute of the Supervising Scientist (eriss) as part of our commitment to the National Centre for Tropical Wetland Research Rick A van Dam Environmental Research Institute of the Supervising Scientist, Locked Bag 2, Jabiru NT 0886, Australia (Present address: Sinclair Knight Merz, 100 Christie St, St Leonards NSW 2065, Australia) David J Walden Environmental Research Institute of the Supervising Scientist, GPO Box 461, Darwin NT 0801, Australia George W Begg Environmental Research Institute of the Supervising Scientist, GPO Box 461, Darwin NT 0801, Australia This report should be cited as follows: van Dam RA, Walden DJ & Begg GW 2002 A preliminary risk assessment of cane toads in Kakadu National Park Scientist Report 164, Supervising Scientist, Darwin NT The Supervising Scientist is part of Environment Australia, the environmental program of the Commonwealth Department of Environment and Heritage © Commonwealth of Australia 2002 Supervising Scientist Environment Australia GPO Box 461, Darwin NT 0801 Australia ISSN 1325-1554 ISBN 0 642 24370 0 This work is copyright Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from the Supervising Scientist Requests and inquiries concerning reproduction -
OWLS of OHIO C D G U I D E B O O K DIVISION of WILDLIFE Introduction O W L S O F O H I O
OWLS OF OHIO c d g u i d e b o o k DIVISION OF WILDLIFE Introduction O W L S O F O H I O Owls have longowls evoked curiosity in In the winter of of 2002, a snowy ohio owl and stygian owl are known from one people, due to their secretive and often frequented an area near Wilmington and two Texas records, respectively. nocturnal habits, fierce predatory in Clinton County, and became quite Another, the Oriental scops-owl, is behavior, and interesting appearance. a celebrity. She was visited by scores of known from two Alaska records). On Many people might be surprised by people – many whom had never seen a global scale, there are 27 genera of how common owls are; it just takes a one of these Arctic visitors – and was owls in two families, comprising a total bit of knowledge and searching to find featured in many newspapers and TV of 215 species. them. The effort is worthwhile, as news shows. A massive invasion of In Ohio and abroad, there is great owls are among our most fascinating northern owls – boreal, great gray, and variation among owls. The largest birds, both to watch and to hear. Owls Northern hawk owl – into Minnesota species in the world is the great gray are also among our most charismatic during the winter of 2004-05 became owl of North America. It is nearly three birds, and reading about species with a major source of ecotourism for the feet long with a wingspan of almost 4 names like fearful owl, barking owl, North Star State. -
Strigiformes) and Lesser Nighthawks (Chodeiles Acutipennis
UNIVERSITY OF CALIFORNIA RIVERSIDE The Evolution of Quiet Flight in Owls (Strigiformes) and Lesser Nighthawks (Chodeiles acutipennis) A Dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Evolution, Ecology, and Organismal Biology by Krista Le Piane December 2020 Dissertation Committee: Dr. Christopher J. Clark, Chairperson Dr. Erin Wilson Rankin Dr. Khaleel A. Razak Copyright by Krista Le Piane 2020 The Dissertation of Krista Le Piane is approved: Committee Chairperson University of California, Riverside ACKNOWLEDGEMENTS I thank my Oral Exam Committee: Dr. Khaleel A. Razak (chairperson), Dr. Erin Wilson Rankin, Dr. Mark Springer, Dr. Jesse Barber, and Dr. Scott Curie. Thank you to my Dissertation Committee: Dr. Christopher J. Clark (chairperson), Dr. Erin Wilson Rankin, and Dr. Khaleel A. Razak for their encouragement and help with this dissertation. Thank you to my lab mates, past and present: Dr. Sean Wilcox, Dr. Katie Johnson, Ayala Berger, David Rankin, Dr. Nadje Najar, Elisa Henderson, Dr. Brian Meyers Dr. Jenny Hazelhurst, Emily Mistick, Lori Liu, and Lilly Hollingsworth for their friendship and support. I thank the Natural History Museum of Los Angeles County (LACM), the California Academy of Sciences (CAS), Museum of Vertebrate Zoology (MVZ) at UC Berkeley, the American Museum of Natural History (ANMH), and the Natural History Museum (NHM) in Tring for access to specimens used in Chapter 1. I would especially like to thank Kimball Garrett and Allison Shultz for help at LACM. I also thank Ben Williams, Richard Jackson, and Reddit user NorthernJoey for permission to use their photos in Chapter 1. Jessica Tingle contributed R code and advice to Chapter 1 and I would like to thank her for her help. -
Conservation Advice Petrogale Concinna Monastria Nabarlek
THREATENED SPECIES SCIENTIFIC COMMITTEE Established under the Environment Protection and Biodiversity Conservation Act 1999 The Minister approved this conservation advice and included this species in the Endangered category, effective from 3/12/15 Conservation Advice Petrogale concinna monastria nabarlek (Kimberley) Note: The information contained in this conservation advice was primarily sourced from ‘The Action Plan for Australian Mammals 2012’ (Woinarski et al., 2014). Any substantive additions obtained during the consultation on the draft are cited within the advice. Readers may note that conservation advices resulting from the Action Plan for Australian Mammals show minor differences in formatting relative to other conservation advices. These reflect the desire to efficiently prepare a large number of advices by adopting the presentation approach of the Action Plan for Australian Mammals, and do not reflect any difference in the evidence used to develop the recommendation. Taxonomy Conventionally accepted as Petrogale concinna monastria (Thomas, 1926). Three subspecies of Petrogale concinna have been described; the other two subspecies are P. c. concinna (nabarlek (Victoria River District)) and P. c. canescens (nabarlek (Top End)). Their validity has not been tested by modern genetic methods, and the geographic bounds (particularly of P. c. concinna and P. c. canescens) are not resolved (Woinarski et al., 2014). However, the subspecies have been accepted by the Australian Faunal Directory. Summary of assessment Conservation status Endangered: Criterion 2 B2(a),b(i)(ii)(iii)(iv)(v) Species can be listed as threatened under state and territory legislation. For information on the listing status of this species under relevant state or territory legislation, see http://www.environment.gov.au/cgi-bin/sprat/public/sprat.pl Reason for conservation assessment by the Threatened Species Scientific Committee This advice follows assessment of new information provided to the Committee to list Petrogale concinna monastria.