Kangaroo and Wallaby Fact Sheet
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Black-Footed Rock Wallaby Factsheet
BLACK-FOOTED ROCK WALLABY FACTSHEET Black-footed rock wallabies are highly agile Brush-tailed rock wallabies are closely related The Threatened Species Network is a macropods able to move bound expertly to the Rothschild's rock wallaby and like them, community-based through very rugged and steep areas. They are very timid, never venturing far from their program of the are found in the arid zone of Central Australia. rock shelters. The two species can be Australian Once widespread in the central desert regions distinguished by to the dorsal stripe, which is Government’s Natural of the Northern Territory, South Australia and not present on the Rothschild's rock wallaby. Heritage Trust and Western Australia, the black-footed rock WWF Australia. wallaby is now found in only a few scattered locations. Where do they live? Black-footed rock wallabies live in rocky escarpment country, gorges, granite outcrops, What do they look like? sandstone cliffs and scree slopes in ranges Black-footed rock wallabies grow to just half a with hummock grassland, occasional fig trees metre tall. They are smaller and much more and low shrubs, caves and coastal limestone finely built than euros (common wallaroo), cliffs. They rely on narrow crevices and small which are found in caves for shelter similar areas. and protection from predators. There are five subspecies of the The stronghold of black-footed rock black-footed rock wallaby, which are wallabies is in the distinguished by their MacDonnell Range geographic range and near Alice Springs differences in their size in the Northern and fur colouration. Territory. -
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. -
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. -
Feratox® As a Humane Control Agent for Wallabies in Tasmania
Feratox® as a Humane Control Agent for Wallabies in Tasmania Mick Statham Tasmanian Institute of Agricultural Research, University of Tasmania, Launceston, Tasmania, and Mt. Pleasant Labs, Kings Meadows, Tasmania, Australia Charles T. Eason Dept. of Ecology, Lincoln University, Lincoln, and Connovation Research Ltd., Auckland, New Zealand Helen L. Statham Tasmanian Institute of Agricultural Research, University of Tasmania, Launceston, Tasmania, Australia Lee Shapiro and Duncan MacMorran Connovation Research Ltd., Auckland, New Zealand ABSTRACT: Compound 1080 has been used to control native wallabies and possums in Tasmania for over 50 years. Public concern in relation to humaneness and its effects on domestic dogs and nontarget species has led to opposition to its use. Feratox®, a form of encapsulated cyanide pellet registered for brushtail possum control in New Zealand, was considered as a replacement toxin. Trials in New Zealand showed that the material is fast-acting and humane in wallabies. In Tasmania, protocols were developed using bait stations that would minimise access by nontarget macropods and wombats. In field trials using Feratox®, however, there was excessive spillage of toxic pellets and variation in bait take between seasons by Tasmanian pademelons. Further work is under way to resolve these issues to see if protocols can be developed for the safe and effective use of cyanide pellets in areas where nontarget mammals are prevalent. KEY WORDS: Australia, bait development, Bennett’s wallaby, brushtail possum, Feratox®, humane toxicants, Macropus rufogriseus, New Zealand, nontarget species, poisons, potassium cyanide, Tasmania, Tasmanian pademelon, Thylogale billardierii, Trichosurus vulpecula, wallaby Proc. 24th Vertebr. Pest Conf. (R. M. Timm and K. A. -
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. -
A Dated Phylogeny of Marsupials Using a Molecular Supermatrix and Multiple Fossil Constraints
Journal of Mammalogy, 89(1):175–189, 2008 A DATED PHYLOGENY OF MARSUPIALS USING A MOLECULAR SUPERMATRIX AND MULTIPLE FOSSIL CONSTRAINTS ROBIN M. D. BECK* School of Biological, Earth and Environmental Sciences, University of New South Wales, Sydney, New South Wales 2052, Australia Downloaded from https://academic.oup.com/jmammal/article/89/1/175/1020874 by guest on 25 September 2021 Phylogenetic relationships within marsupials were investigated based on a 20.1-kilobase molecular supermatrix comprising 7 nuclear and 15 mitochondrial genes analyzed using both maximum likelihood and Bayesian approaches and 3 different partitioning strategies. The study revealed that base composition bias in the 3rd codon positions of mitochondrial genes misled even the partitioned maximum-likelihood analyses, whereas Bayesian analyses were less affected. After correcting for base composition bias, monophyly of the currently recognized marsupial orders, of Australidelphia, and of a clade comprising Dasyuromorphia, Notoryctes,and Peramelemorphia, were supported strongly by both Bayesian posterior probabilities and maximum-likelihood bootstrap values. Monophyly of the Australasian marsupials, of Notoryctes þ Dasyuromorphia, and of Caenolestes þ Australidelphia were less well supported. Within Diprotodontia, Burramyidae þ Phalangeridae received relatively strong support. Divergence dates calculated using a Bayesian relaxed molecular clock and multiple age constraints suggested at least 3 independent dispersals of marsupials from North to South America during the Late Cretaceous or early Paleocene. Within the Australasian clade, the macropodine radiation, the divergence of phascogaline and dasyurine dasyurids, and the divergence of perameline and peroryctine peramelemorphians all coincided with periods of significant environmental change during the Miocene. An analysis of ‘‘unrepresented basal branch lengths’’ suggests that the fossil record is particularly poor for didelphids and most groups within the Australasian radiation. -
A Species-Level Phylogenetic Supertree of Marsupials
J. Zool., Lond. (2004) 264, 11–31 C 2004 The Zoological Society of London Printed in the United Kingdom DOI:10.1017/S0952836904005539 A species-level phylogenetic supertree of marsupials Marcel Cardillo1,2*, Olaf R. P. Bininda-Emonds3, Elizabeth Boakes1,2 and Andy Purvis1 1 Department of Biological Sciences, Imperial College London, Silwood Park, Ascot SL5 7PY, U.K. 2 Institute of Zoology, Zoological Society of London, Regent’s Park, London NW1 4RY, U.K. 3 Lehrstuhl fur¨ Tierzucht, Technical University of Munich, Alte Akademie 12, 85354 Freising-Weihenstephan, Germany (Accepted 26 January 2004) Abstract Comparative studies require information on phylogenetic relationships, but complete species-level phylogenetic trees of large clades are difficult to produce. One solution is to combine algorithmically many small trees into a single, larger supertree. Here we present a virtually complete, species-level phylogeny of the marsupials (Mammalia: Metatheria), built by combining 158 phylogenetic estimates published since 1980, using matrix representation with parsimony. The supertree is well resolved overall (73.7%), although resolution varies across the tree, indicating variation both in the amount of phylogenetic information available for different taxa, and the degree of conflict among phylogenetic estimates. In particular, the supertree shows poor resolution within the American marsupial taxa, reflecting a relative lack of systematic effort compared to the Australasian taxa. There are also important differences in supertrees based on source phylogenies published before 1995 and those published more recently. The supertree can be viewed as a meta-analysis of marsupial phylogenetic studies, and should be useful as a framework for phylogenetically explicit comparative studies of marsupial evolution and ecology. -
Australian Journal of Earth Sciences Paleosol Record of Neogene Climate
This article was downloaded by: [Retallack, Gregory J.][University of Oregon] On: 28 September 2010 Access details: Access Details: [subscription number 917394740] Publisher Taylor & Francis Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House, 37- 41 Mortimer Street, London W1T 3JH, UK Australian Journal of Earth Sciences Publication details, including instructions for authors and subscription information: http://www.informaworld.com/smpp/title~content=t716100753 Paleosol record of Neogene climate change in the Australian outback C. A. Metzgera; G. J. Retallacka a Department of Geological Sciences, University of Oregon, Eugene, OR, USA Online publication date: 24 September 2010 To cite this Article Metzger, C. A. and Retallack, G. J.(2010) 'Paleosol record of Neogene climate change in the Australian outback', Australian Journal of Earth Sciences, 57: 7, 871 — 885 To link to this Article: DOI: 10.1080/08120099.2010.510578 URL: http://dx.doi.org/10.1080/08120099.2010.510578 PLEASE SCROLL DOWN FOR ARTICLE Full terms and conditions of use: http://www.informaworld.com/terms-and-conditions-of-access.pdf This article may be used for research, teaching and private study purposes. Any substantial or systematic reproduction, re-distribution, re-selling, loan or sub-licensing, systematic supply or distribution in any form to anyone is expressly forbidden. The publisher does not give any warranty express or implied or make any representation that the contents will be complete or accurate or up to date. The accuracy of any instructions, formulae and drug doses should be independently verified with primary sources. The publisher shall not be liable for any loss, actions, claims, proceedings, demand or costs or damages whatsoever or howsoever caused arising directly or indirectly in connection with or arising out of the use of this material. -
Conservation Science Western Australia 5, 12–18
Conservation Science W. Aust. 9 (3) : 239–248 (2015) The diet of foxes (Vulpes vulpes) in fragmented Wheatbelt reserves in Western Australia: implications for woylies (Bettongia penicillata) and other native fauna NICOLA J MARLOW ab *, ANDREW AE WILLIAMS ab, NEIL D THOMAS ab, BRIAN MACMAHON b AND JOHN LAWSON b a Department of Parks and Wildlife, PO Box 51 Wanneroo, WA 6946, Australia b Invasive Animals Co-operative Research Centre 48 Oxford Street, Adelaide, SA 5061, Australia * Corresponding author: [email protected] ABSTRACT The diet of foxes in two fragmented Wheatbelt reserves in south-west Western Australia, Dryandra Woodland (DW) and Tutanning Nature Reserve (TNR), was investigated. Fox baiting commenced in these reserves in the early 1980s and the trap success of woylies (Bettongia penicillata), a threatened species, increased significantly. Woylie capture rates were sustained in TNR until 1992 and in DW until 2000 but then decreased suddenly despite ongoing fox control. The diet of foxes was investigated as part of a larger study examining the reasons for the woylie decline. The contents of 283 fox scats from DW and TNR, and 167 scats from two unbaited sites, Quinns block (QB) and Highbury block (HB), were analysed volumetrically to determine the relative importance of each dietary item. The actual consumption of each item was calculated using digestibility estimates. In baited sites the foxes’ main dietary components were house mice (Mus domesticus, 28%), carrion (sheep, Ovis aries and western grey kangaroo, Macropus fuliginosus; 26%) and rabbits (Oryctolagus cuniculus, 17%). In unbaited sites the main components were carrion (predominately sheep, 60%) and some invertebrates (13%). -
The Relationships of the Potoroidae to the Macropodidae (Marsupialia) M
PAP. & Paoc. RoY. Soc. TA~MANIA, 1949 ( 15Tff SEPTEMBER, 1950) The Relationships of the Potoroidae to the Macropodidae (Marsupialia) m By JOSEPH PEARSON Tawman'ian fi!Insenm (Read lst November, 1H4!J) IVITH 21 TEXT FwUJu;s INTRODUCTION There is perhaps no gToup of mammals to which so much attention has been directed as the Marsupialia and the interests of investigators have been particularly concerned with the relationships and phylogeny of the Order. But in spite of a very considerable literature dealing with speculations on these problems we are still in doubt as to which classification would give the best picture of the phylo genetic relationships of the gnmp. Owen's division of the ma1·supials into Poly protodontia and Diprotodontia(2), though having much to commend it, is hardly mon satisfactory than the division into Diadactyla and Syndactyla which was first suggested by de Blainville in 18;)4. Both break down hopelessly before the paradox of the Pm·ameloidea and the enigma of the Caenolestoidea. Owing to the imper fections of the geologiqd record the palaeontology of Australian marsupials has littlt> to offer as a contl·ilmtion to the main pl'Oblems. Thus we are thrown back upon the study of the comparative anatmny and embryology of recent forms. In the present paper we are not concerned with one of these major phylogenetic JH·oblems. The question to be discussed is whether the true kangaroos and rat kangaroos possess sufficient fundamental characters in common to justify their being placed in the same family, as is almost universally held by systematists at the present day. -
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