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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. -
Can Kangaroos Survive in the Wheatbelt?
Journal of the Department of Agriculture, Western Australia, Series 4 Volume 31 Number 1 1990 Article 4 1-1-1990 Can kangaroos survive in the wheatbelt? Graham Arnold Follow this and additional works at: https://researchlibrary.agric.wa.gov.au/journal_agriculture4 Part of the Biodiversity Commons, Environmental Monitoring Commons, and the Other Animal Sciences Commons Recommended Citation Arnold, Graham (1990) "Can kangaroos survive in the wheatbelt?," Journal of the Department of Agriculture, Western Australia, Series 4: Vol. 31 : No. 1 , Article 4. Available at: https://researchlibrary.agric.wa.gov.au/journal_agriculture4/vol31/iss1/4 This article is brought to you for free and open access by Research Library. It has been accepted for inclusion in Journal of the Department of Agriculture, Western Australia, Series 4 by an authorized administrator of Research Library. For more information, please contact [email protected]. Can kangaroos survive in the wheaibelt? mm mmmm By Graham Arnold, Senior Principal Research Scientist, CSIRO Division of Wildlife and Ecology, Helena Valley One of the costs of agricultural development in Western Australia over the past 100 years has been the loss of most of the native vegetation and, consequently, massive reductions in the numbers of most of our native fauna. Thirteen mammal species are extinct and many bird and mammal species are extinct in some areas. These losses will increase as remnant native vegetation degrades under the impact of nutrients washed and blown from farmland, from the invasion by Western grey kangaroo grazing weeds and from grazing sheep. on pasture in the early morning. Even kangaroos are affected. -
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. -
Encouraging Possums
Encouraging Possums Keywords: possums, mammals, habitat, management, nest boxes Location: southwest Author: Emma Bramwell Possums are delightful and appealing creatures, with THE SEVEN SPECIES their soft downy fur and large innocent eyes. Some may be as small as a mouse while others are the size of a domestic • Honeypossum Tarsipes rostratus cat. The honey possum is the smallest of the Western The western ringtail and common brushtail possums are Australian possums, and is endemic to (occurring only in) two of the most commonly seen native animals around urban the lower southwest, in heaths with a rich diversity of areas in the southwest of Western Australia. The common nectar-producing plants. brushtail possum in particular has adapted to urban Mainly nocturnal, the honey possum sleeps during the development, and readily takes up residence in human day in hollow stems or abandoned bird nests, emerging at dwellings. With careful planning and management, people night to feed on the nectar and pollen that exclusively make can live harmoniously with these creatures and enjoy the up its diet, probing flowers with its long, pointed snout and close proximity of wildlife. brush-tipped tongue. In colder weather the honey possum becomes torpid (semi-hibernates). The honey possum has no obvious breeding season. WHAT IS A POSSUM? Most young are produced when pollen and nectar are most abundant, and females usually raise two or three young at a A number of small to medium-sized, tree-climbing time. Australian marsupial species have been given the common Provided large areas of habitat are retained, the honey name of possum. -
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. -
Local Population Structure of a Naturally Occurring Metapopulation of the Quokka (Setonix Brachyurus Macropodidae: Marsupialia)
Biological Conservation 110 (2003) 343–355 www.elsevier.com/locate/biocon Local population structure of a naturally occurring metapopulation of the quokka (Setonix brachyurus Macropodidae: Marsupialia) Matt W. Haywarda,b,c,*, Paul J. de Toresb,c, Michael J. Dillonc, Barry J. Foxa aSchool of Biological, Earth and Environmental Science, University of New South Wales, Sydney, NSW 2052, Australia bDepartment of Conservation and Land Management, Wildlife Research Centre, PO Box 51 Wanneroo, WA6946, Australia cDepartment of Conservation and Land Management, Dwellingup Research Centre, Banksiadale Road, Dwellingup, WA6213, Australia Received 8 May 2002; received in revised form 18 July 2002; accepted 22 July 2002 Abstract We investigated the population structure of the quokka (Setonix brachyurus) on the mainland of Western Australia using mark– recapture techniques. Seven previously known local populations and one unconfirmed site supporting the preferred, patchy and discrete, swampy habitat of the quokka were trapped. The quokka is now considered as locally extinct at three sites. The five remaining sites had extremely low numbers, ranging from 1 to 36 individuals. Population density at these sites ranged from 0.07 to 4.3 individuals per hectare. There has been no response to the on-going, 6 year fox control programme occurring in the region despite the quokkas’ high fecundity and this is due to low recruitment levels. The remaining quokka populations in the northern jarrah forest appear to be the terminal remnants of a collapsing metapopulation. # 2002 Elsevier Science Ltd. All rights reserved. Keywords: Population structure; Predation; Reproduction; Setonix brachyurus; Vulnerable 1. Introduction The Rottnest Island quokka population fluctuates around 5000 with peaks of 10,000 individuals (Waring, The quokka (Setonix brachyurus Quoy & Gaimard 1956). -
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. -
A Phylogeny and Timescale for Marsupial Evolution Based on Sequences for Five Nuclear Genes
J Mammal Evol DOI 10.1007/s10914-007-9062-6 ORIGINAL PAPER A Phylogeny and Timescale for Marsupial Evolution Based on Sequences for Five Nuclear Genes Robert W. Meredith & Michael Westerman & Judd A. Case & Mark S. Springer # Springer Science + Business Media, LLC 2007 Abstract Even though marsupials are taxonomically less diverse than placentals, they exhibit comparable morphological and ecological diversity. However, much of their fossil record is thought to be missing, particularly for the Australasian groups. The more than 330 living species of marsupials are grouped into three American (Didelphimorphia, Microbiotheria, and Paucituberculata) and four Australasian (Dasyuromorphia, Diprotodontia, Notoryctemorphia, and Peramelemorphia) orders. Interordinal relationships have been investigated using a wide range of methods that have often yielded contradictory results. Much of the controversy has focused on the placement of Dromiciops gliroides (Microbiotheria). Studies either support a sister-taxon relationship to a monophyletic Australasian clade or a nested position within the Australasian radiation. Familial relationships within the Diprotodontia have also proved difficult to resolve. Here, we examine higher-level marsupial relationships using a nuclear multigene molecular data set representing all living orders. Protein-coding portions of ApoB, BRCA1, IRBP, Rag1, and vWF were analyzed using maximum parsimony, maximum likelihood, and Bayesian methods. Two different Bayesian relaxed molecular clock methods were employed to construct a timescale for marsupial evolution and estimate the unrepresented basal branch length (UBBL). Maximum likelihood and Bayesian results suggest that the root of the marsupial tree is between Didelphimorphia and all other marsupials. All methods provide strong support for the monophyly of Australidelphia. Within Australidelphia, Dromiciops is the sister-taxon to a monophyletic Australasian clade.