The Kangaroo Island Tammar Wallaby
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Red-Necked Wallaby (Bennett’S Wallaby) Macropus Rufogriseus
Red-necked Wallaby (Bennett’s Wallaby) Macropus rufogriseus Class: Mammalia Order: Diprotodontia Family: Macropodidae Characteristics: Red-necked wallabies get their name from the red fur on the back of their neck. They are also differentiated from other wallabies by the white cheek patches and larger size compared to other wallaby species (Bioweb). The red-necked wallaby’s body fur is grey to reddish in color with a white or pale grey belly. Their muzzle, paws and toes are black (Australia Zoo). Wallabies look like smaller kangaroos with their large hindquarters, short forelimbs, and long, muscular tails. The average size of this species is 27-32 inches in the body with a tail length of 20-28 inches. The females weigh about 25 pounds while the males weigh significantly more at 40 pounds. The females differ from the males of the species in that they have a forward opening pouch (Sacramento Zoo). Range & Habitat: Flat, high-ground eucalyptus Behavior: Red-necked wallabies are most active at dawn and dusk to avoid forests near open grassy areas in the mid-day heat. In the heat, they will lick their hands and forearms to Tasmania and South-eastern promote heat loss. (Animal Diversity) These wallabies are generally solitary Australia. but do forage in small groups. The males will have boxing matches with one another to determine social hierarchy within populations. They can often be seen punching, wrestling, skipping, dancing, standing upright, grabbing, sparring, pawing, and kicking. All members of the kangaroo and wallaby family travel by hopping. Red-necked wallabies can hop up to 6 feet in the air. -
Tammar Wallaby Macropus Eugenii (Desmarest, 1817)
Tammar Wallaby Macropus eugenii (Desmarest, 1817) Description Dark, grizzled grey-brown above, becoming rufous on the sides of the body and the limbs, especially in males. Pale grey-buff below. Other Common Names Dama Wallaby (South Australia) Distribution The Western Australian subspecies of the Tammar Wallaby was previously distributed throughout most of the south-west of Western Australia from Kalbarri National Park to Cape Arid on the south coast Photo: Babs & Bert Wells/DEC and extending to western parts of the Wheat belt. Size The Tammar Wallaby is currently known to inhabit three islands in the Houtman Abrolhos group (East and West Wallabi Island, and an introduced population on North Island), Garden Island near Perth, Kangaroo Island wallabies Middle and North Twin Peak Islands in the Archipelago of the Head and body length Recherche, and several sites on the mainland - including, Dryandra, Boyagin, Tutanning, Batalling (reintroduced), Perup, private property 590-680 mm in males near Pingelly, Jaloran Road timber reserve near Wagin, Hopetoun, 520-630 mm in females Stirling Range National Park, and Fitzgerald River National Park. The Tammar Wallaby remains relatively abundant at these sites which Tail length are subject to fox control. 380-450 mm in males They have been reintroduced to the Darling scarp near Dwellingup, 330-440 mm in females Julimar Forest near Bindoon, state forest east of Manjimup, Avon Valley National Park, Walyunga National Park, Nambung National Park and to Karakamia and Paruna Sanctuaries. Weight For further information regarding the distribution of this species Western Australian wallabies please refer to www.naturemap.dec.wa.gov.au 2.9-6.1 kg in males Habitat 2.3-4.3 kg in females Dense, low vegetation for daytime shelter and open grassy areas for feeding. -
Ecology of the Koala, Phascolarctos Cinereus
I give eonsent to this eopy of ny thesis, r,,rhen d.eposited. in the Universit.y Library, being avail-abl-e 1'or loan and. photocopying. Date . ?! ÛP,"+ .13:r.o.. S igned. CONTENTS SUM MA RY ACKNOWLEDGEMENTS lil INTRODUCTION I PA,RT I FIELD STUDIES INTRODUCTION O.l Kongoroo lslqnd B O.2 Floro ond Founo il 0.3 Philpott's Study l3 O.4 Methods t5 0.5 Results 25 I THE DISTRIBUTION AND ABUN DANCE OF KOALAS I. I The Distribution of Koalos 29 | .2 The Abundonce of Koo lqs 34 2 BREEDING, GROWTH AND DEVELOPA,\E¡.¡T 2.1 Breeding 39 2.2 Pouch Young 40 2.3 Growth, Ageing ond LongevitY 49 2.4 Sexucrl Moturity 54 I SUMMARY The distribution of koalas u'ithin Flinders Chase was fou-nd to be made up of areas centred on the occurrences of manna guilr , Euca.ly¡rtus viminalis. Some koalas br:owsed chiefly iri trees of other species but tlrere liÌere ferv animals, if any, that clid not feed on the foliage of E. r'iminalis rnore or less regularly. The composition of populations in sever¿rl sürcly areas changed from üirne to time but over aE long as three successir¡e years of observat:lorr the numhers remained ::emarkably constant. The koalas bred in the surnmer: arrd early auturnn, and a high proporüon of feinales successfully raised a single young to independence each year. Growth of the yourìg was :lapid over the first Lhree yearr!; it slowed. down thereafter and anirnals reached firll size in tlieir fourth and fiffh years. -
Antipredator Behaviour of Red-Necked Pademelons: a Factor Contributing to Species Survival?
Animal Conservation (2002) 5, 325–331 © 2002 The Zoological Society of London DOI:10.1017/S1367943002004080 Printed in the United Kingdom Antipredator behaviour of red-necked pademelons: a factor contributing to species survival? Daniel T. Blumstein1,2, Janice C. Daniel1,2, Marcus R. Schnell2,3, Jodie G. Ardron2,4 and Christopher S. Evans4 1 Department of Organismic Biology, Ecology and Evolution, 621 Charles E. Young Drive South, University of California, Los Angeles, CA 90095-1606, USA 2 Cooperative Research Centre for the Conservation and Management of Marsupials, Macquarie University, Sydney, NSW 2109, Australia 3 Department of Biological Sciences, Macquarie University, Sydney, NSW 2109, Australia 4 Department of Psychology, Macquarie University, Sydney, NSW 2109, Australia (Received 15 January 2002; accepted 17 June 2002) Abstract Australian mammals have one of the world’s worst records of recent extinctions. A number of stud- ies have demonstrated that red foxes (Vulpes vulpes) have a profound effect on the population biol- ogy of some species. However, not all species exposed to fox predation have declined. We studied the antipredator behaviour of a species that has not declined – the red-necked pademelon (Thylogale thetis), and contrasted it with previous studies on a species that has declined – the tammar wallaby (Macropus eugenii), to try to understand behavioural factors associated with survival. We focused on two antipredator behaviours: predator recognition and the way in which antipredator vigilance is influ- enced by the presence of conspecifics. We found that predator-naïve pademelons responded to the sight of certain predators, suggesting that they had some degree of innate recognition ability. -
Energetics and Biomechanics of Locomotion by Red Kangaroos (Macropus Rufus)
Comparative Biochemistry and Physiology Part B 120 (1998) 41–49 Review Energetics and biomechanics of locomotion by red kangaroos (Macropus rufus) Rodger Kram a,*, Terence J. Dawson b a Department of Integrati6e Biology, Uni6ersity of California, Berkeley CA 94720-3140, USA b School of Biological Sciences, Uni6ersity of New South Wales, Sydney NSW 2052, Australia Received 15 May 1997; received in revised form 22 September 1997; accepted 7 October 1997 Abstract As red kangaroos hop faster over level ground, their rate of oxygen consumption (indicating metabolic energy consumption) remains nearly the same. This phenomenon has been attributed to exceptional elastic energy storage and recovery via long compliant tendons in the legs. Alternatively, red kangaroos may have exceptionally efficient muscles. To estimate efficiency, we measured the metabolic cost of uphill hopping, where muscle fibers must perform mechanical work against gravity. We found that −1 uphill hopping was much more expensive than level hopping. The maximal rate of oxygen consumption measured (3 ml O2 kg s−1) exceeds all but a few vertebrate species. However, efficiency values were normal, 30%. At faster level hopping speeds the effective mechanical advantage of the extensor muscles of the ankle joint remained the same. Thus, kangaroos generate the same muscular force at all speeds but do so more rapidly at faster hopping speeds. This contradicts a recent hypothesis for what sets the cost of locomotion. The cost of transport (J kg−1 m−1) decreases at faster hopping speeds, yet red kangaroos prefer to use relatively slow speeds that avoid high levels of tendon stress. © 1998 Elsevier Science Inc. -
Macropod Herpesviruses Dec 2013
Herpesviruses and macropods Fact sheet Introductory statement Despite the widespread distribution of herpesviruses across a large range of macropod species there is a lack of detailed knowledge about these viruses and the effects they have on their hosts. While they have been associated with significant mortality events infections are usually benign, producing no or minimal clinical effects in their adapted hosts. With increasing emphasis being placed on captive breeding, reintroduction and translocation programs there is a greater likelihood that these viruses will be introduced into naïve macropod populations. The effects and implications of this type of viral movement are unclear. Aetiology Herpesviruses are enveloped DNA viruses that range in size from 120 to 250nm. The family Herpesviridae is divided into three subfamilies. Alphaherpesviruses have a moderately wide host range, rapid growth, lyse infected cells and have the capacity to establish latent infections primarily, but not exclusively, in nerve ganglia. Betaherpesviruses have a more restricted host range, a long replicative cycle, the capacity to cause infected cells to enlarge and the ability to form latent infections in secretory glands, lymphoreticular tissue, kidneys and other tissues. Gammaherpesviruses have a narrow host range, replicate in lymphoid cells, may induce neoplasia in infected cells and form latent infections in lymphoid tissue (Lachlan and Dubovi 2011, Roizman and Pellet 2001). There have been five herpesvirus species isolated from macropods, three alphaherpesviruses termed Macropodid Herpesvirus 1 (MaHV1), Macropodid Herpesvirus 2 (MaHV2), and Macropodid Herpesvirus 4 (MaHV4) and two gammaherpesviruses including Macropodid Herpesvirus 3 (MaHV3), and a currently unclassified novel gammaherpesvirus detected in swamp wallabies (Wallabia bicolor) (Callinan and Kefford 1981, Finnie et al. -
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. -
The Meeting of Matthew Flinders and Nicolas Baudin
A Cordial Encounter? 53 A Cordial Encounter? The Meeting of Matthew Flinders and Nicolas Baudin (8-9 April, 1802) Jean Fornasiero and John West-Sooby1 The famous encounter between Nicolas Baudin and Matthew Flinders in the waters off Australia’s previously uncharted south coast has now entered the nation’s folklore. At a time when their respective countries were locked in conflict at home and competing for strategic advantage on the world stage, the two captains were able to set aside national rivalries and personal disappointments in order to greet one another with courtesy and mutual respect. Their meeting is thus portrayed as symbolic of the triumph of international co-operation over the troubled geopolitics of the day. What united the two expeditions—the quest for knowledge in the spirit of the Enlightenment—proved to be stronger than what divided them. This enduring—and endearing—image of the encounter between Baudin and Flinders is certainly well supported by the facts as we know them. The two captains did indeed conduct themselves on that occasion in an exemplary manner, readily exchanging information about their respective discoveries and advising one another about the navigational hazards they should avoid or about safe anchorages where water and other supplies could be obtained. Furthermore, the civility of their meeting points to a strong degree of mutual respect, and perhaps also to a recognition of their shared experience as navigators whom fate had thrown together on the lonely and treacherous shores of the “unknown coast” of Australia. And yet, as appealing as it may be, this increasingly idealized image of the encounter runs the risk of masking some of its subtleties and complexities. -
Reproductionreview
REPRODUCTIONREVIEW Wombat reproduction (Marsupialia; Vombatidae): an update and future directions for the development of artificial breeding technology Lindsay A Hogan1, Tina Janssen2 and Stephen D Johnston1,2 1Wildlife Biology Unit, Faculty of Science, School of Agricultural and Food Sciences, The University of Queensland, Gatton 4343, Queensland, Australia and 2Australian Animals Care and Education, Mt Larcom 4695, Queensland, Australia Correspondence should be addressed to L A Hogan; Email: [email protected] Abstract This review provides an update on what is currently known about wombat reproductive biology and reports on attempts made to manipulate and/or enhance wombat reproduction as part of the development of artificial reproductive technology (ART) in this taxon. Over the last decade, the logistical difficulties associated with monitoring a nocturnal and semi-fossorial species have largely been overcome, enabling new features of wombat physiology and behaviour to be elucidated. Despite this progress, captive propagation rates are still poor and there are areas of wombat reproductive biology that still require attention, e.g. further characterisation of the oestrous cycle and oestrus. Numerous advances in the use of ART have also been recently developed in the Vombatidae but despite this research, practical methods of manipulating wombat reproduction for the purposes of obtaining research material or for artificial breeding are not yet available. Improvement of the propagation, genetic diversity and management of wombat populations requires a thorough understanding of Vombatidae reproduction. While semen collection and cryopreservation in wombats is fairly straightforward there is currently an inability to detect, induce or synchronise oestrus/ovulation and this is an impeding progress in the development of artificial insemination in this taxon. -
Kangaroos, Dendrolagus Matschiei (Macropodidae), in Upper Montane Forest
Spatial Requirements of Free-Ranging Huon Tree Kangaroos, Dendrolagus matschiei (Macropodidae), in Upper Montane Forest Gabriel Porolak1,2,3*, Lisa Dabek3, Andrew K. Krockenberger1,2 1 Centre for Tropical Biodiversity and Climate Change, James Cook University, Cairns, Australia, 2 School of Marine and Tropical Biology, James Cook University, Cairns, Australia, 3 Department of Field Conservation, Woodland Park Zoo, Seattle, Washington, United States of America Abstract Tree kangaroos (Macropodidae, Dendrolagus) are some of Australasia’s least known mammals. However, there is sufficient evidence of population decline and local extinctions that all New Guinea tree kangaroos are considered threatened. Understanding spatial requirements is important in conservation and management. Expectations from studies of Australian tree kangaroos and other rainforest macropodids suggest that tree kangaroos should have small discrete home ranges with the potential for high population densities, but there are no published estimates of spatial requirements of any New Guinea tree kangaroo species. Home ranges of 15 Huon tree kangaroos, Dendrolagus matschiei, were measured in upper montane forest on the Huon Peninsula, Papua New Guinea. The home range area was an average of 139.6626.5 ha (100% MCP; n = 15) or 81.8628.3 ha (90% harmonic mean; n = 15), and did not differ between males and females. Home ranges of D. matschiei were 40–100 times larger than those of Australian tree kangaroos or other rainforest macropods, possibly due to the impact of hunting reducing density, or low productivity of their high altitude habitat. Huon tree kangaroos had cores of activity within their range at 45% (20.964.1 ha) and 70% (36.667.5 ha) harmonic mean isopleths, with little overlap (4.862.9%; n = 15 pairs) between neighbouring females at the 45% isopleth, but, unlike the Australian species, extensive overlap between females (20.865.5%; n = 15 pairs) at the complete range (90% harmonic mean). -
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.