Skulls of Tasmania
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Reptile-Like Physiology in Early Jurassic Stem-Mammals
bioRxiv preprint doi: https://doi.org/10.1101/785360; this version posted October 10, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Title: Reptile-like physiology in Early Jurassic stem-mammals Authors: Elis Newham1*, Pamela G. Gill2,3*, Philippa Brewer3, Michael J. Benton2, Vincent Fernandez4,5, Neil J. Gostling6, David Haberthür7, Jukka Jernvall8, Tuomas Kankanpää9, Aki 5 Kallonen10, Charles Navarro2, Alexandra Pacureanu5, Berit Zeller-Plumhoff11, Kelly Richards12, Kate Robson-Brown13, Philipp Schneider14, Heikki Suhonen10, Paul Tafforeau5, Katherine Williams14, & Ian J. Corfe8*. Affiliations: 10 1School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK. 2School of Earth Sciences, University of Bristol, Bristol, UK. 3Earth Science Department, The Natural History Museum, London, UK. 4Core Research Laboratories, The Natural History Museum, London, UK. 5European Synchrotron Radiation Facility, Grenoble, France. 15 6School of Biological Sciences, University of Southampton, Southampton, UK. 7Institute of Anatomy, University of Bern, Bern, Switzerland. 8Institute of Biotechnology, University of Helsinki, Helsinki, Finland. 9Department of Agricultural Sciences, University of Helsinki, Helsinki, Finland. 10Department of Physics, University of Helsinki, Helsinki, Finland. 20 11Helmholtz-Zentrum Geesthacht, Zentrum für Material-und Küstenforschung GmbH Germany. 12Oxford University Museum of Natural History, Oxford, OX1 3PW, UK. 1 bioRxiv preprint doi: https://doi.org/10.1101/785360; this version posted October 10, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 13Department of Anthropology and Archaeology, University of Bristol, Bristol, UK. 14Faculty of Engineering and Physical Sciences, University of Southampton, Southampton, UK. -
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. -
The Structure-Function Relationship of the Lung of the Australian Sea Lion Neophoca Cinerea
The Structure-Function Relationship of the Lung of the Australian Sea Liont Neophoc e clnerea by Anthony Nicholson B.V.Sc. A thesis submitted for the degree of Doctor of PhilosoPhY' Department of PathologY' UniversitY of Adelaide February 1984 Frontispiece: Group of four adull female Australian sea lions basking in the sun at Seal Bay, Kangaroo Island. ËF:æ: oo',,, 'å¡ -*-d, l--- --a - .¡* É--- .-\tb.<¡- <} b' \ .ltl '' 4 qÙ CONTENTS Page List of Figures X List of Tables xi Abstract XIV Declaration XV Acknowledge m ents I I. Introduction Chapter \ I I.I Classification of Marine Mammals I I.2', Distribution of Australian Pinnipeds 2 I.3 Diving CaPabilitY 3 PhYsiologY 1.4 Diving 4 Cardiovascular SYstem ' l'.4.I B I.4.2 OxYgen Stores 1l L.4.3 BiochemicalAdaPtations L3 I.4.4 PulmonarYFunction I.4.5 Effects oi Incteased Hydrostatic Pressure T6 l-8 1.5 SummarY and Aims 20 Chapter 2. Materials and Methods 20 ?.I Specimen Collection 2I 2.2 Lung Fixation 2I 2.3 Lung Votume Determination 22 2.4 Parasite Collection and Incubation 22 2.5 M icroscoPY 22 2.5.I Light MicroscoPY Electron Microscopy 23 2..5.2 Trãnsmission 23 2.5.3 Scanning ElectronMicroscopy 25 Chapter 5. Norm al ResPiratorY Structure 25 t.r Introduction 25 Mam maI Respiratory System 3.2 Terrestrial 25 1.2.I MacroscoPtc 27 3.2.2 MicroscoPic 27 SYstem 3.3 Pinniped ResPiratorY 27 3.3.I MacroscoPic 28 3.3.2 MicroscoPic 3I 3.4 Results 3I 1.4.L MacroscoPic 32 3.4.2 MicroscoPic 7B 3.5 Discussion 7B 3.5.I MacroscoPtc 79 3.5.2 MicroscoPic 92 3.6 SummarY IV Page Chapter 4. -
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. -
090303 Long Footed Potoroo Skull Yalmy Rd
Pre-Logging Report of Coupes 846-502-0003, 846-502-0010 and 846-502-0013 Orbost District Study location Between junction of Yalmy River and Little Yalmy River Coupee Numbers 846-502-0003, 846-502-0010, 846-502-0013 Date 3 March 2009 Organisation Fauna and Flora Research Collective - East Gippsland Permit No. 10004865 (File No: FF383119) Motive of research To ascertain the ecological significance of specific areas currently proposed for logging. Aim of study The aim of this study is to ascertain and verify if coupes 846-502- 0003, 846-502-0010 and 846-502-0013 support rare or endangered fauna listed in the East Gippsland Forest Management Plan. Table 1: Recorded Common name Scientific name species on 01-02/03/09 Long-Footed Potoroo Potorous longipes Sooty Owl Tyto tenebricosa Southern Boobook Owl Ninox novaehollandiae Greater Glider Petauroides volans Sugar Glider Petaurus breviceps Method of Study 1. Walking through the proposed coupes to observe tracks, habitat, and feeding and defecation signs of fauna. 2. The surveying of the key species with the aid of acoustic equipment and spotlights. The goal is to observe individual animals visually or identify them by their calls. The fieldwork is ideally preformed on warm nights without rain on which greater activity can be recorded. Fieldwork should be commenced at dusk. Poor conditions provide a greater false absence rate 1 in relation to good conditions that provide a lower false absence rate. Date of study 1 - 2 March 2009 Surveyors of Mr. P. Calle, Mr. A. Lincoln habitat Surveyors of Mr. P. Calle, Mr. -
Project Deliverance the Response of ‘Critical-Weight-Range’ Mammals to Effective Fox Control in Mesic Forest Habitats in Far East Gippsland, Victoria
Project Deliverance The response of ‘critical-weight-range’ mammals to effective fox control in mesic forest habitats in far East Gippsland, Victoria A Victorian Government Initiative Project Deliverance: the response of ‘critical-weight-range’ mammals to effective fox control in mesic forest habitats in far East Gippsland, Victoria Department of Sustainability and Environment Project Deliverance The response of ‘critical-weight-range’ mammals to effective fox control in mesic forest habitats in far East Gippsland, Victoria A Victorian Government Initiative Publisher/Further information - Department of Sustainability and Environment, PO Box 500, East Melbourne, Victoria, Australia, 3002. Web: http://www.dse.vic.gov.au First published 2006. © The State of Victoria, Department of Sustainability and Environment, 2006 All rights reserved. This document is subject to the Copyright Act 1968. 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 or otherwise without the prior permission of the publisher. Copyright in photographs remains with the photographers mentioned in the text. ISBN 1 74152 343 5 Disclaimer—This publication may be of assistance to you but the State of Victoria and its employees do not guarantee that the publication is without flaw of any kind or is wholly appropriate for your particular purpose and therefore disclaims all liability for any error, loss or other consequence which may arise from you relying on any information in this publication. Citation— Murray, A.J., Poore, R.N. and Dexter, N. (2006). Project Deliverance—the response of ‘critical weight range’ mammals to effective fox control in mesic forest habitats in far East Gippsland, Victoria. -
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. -
Yellow Bellied Glider
Husbandry Manual for the Yellow-Bellied Glider Petaurus australis [Mammalia / Petauridae] Liana Carroll December 2005 Western Sydney Institute of TAFE, Richmond 1068 Certificate III Captive Animals Lecturer: Graeme Phipps TABLE OF CONTENTS 1 INTRODUCTION............................................................................................................................... 5 2 TAXONOMY ...................................................................................................................................... 6 2.1 NOMENCLATURE .......................................................................................................................... 6 2.2 SUBSPECIES .................................................................................................................................. 6 2.3 RECENT SYNONYMS ..................................................................................................................... 6 2.4 OTHER COMMON NAMES ............................................................................................................. 6 3 NATURAL HISTORY ....................................................................................................................... 7 3.1 MORPHOMETRICS ......................................................................................................................... 8 3.1.1 Mass And Basic Body Measurements ..................................................................................... 8 3.1.2 Sexual Dimorphism ................................................................................................................ -
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. -
MORNINGTON PENINSULA BIODIVERSITY: SURVEY and RESEARCH HIGHLIGHTS Design and Editing: Linda Bester, Universal Ecology Services
MORNINGTON PENINSULA BIODIVERSITY: SURVEY AND RESEARCH HIGHLIGHTS Design and editing: Linda Bester, Universal Ecology Services. General review: Sarah Caulton. Project manager: Garrique Pergl, Mornington Peninsula Shire. Photographs: Matthew Dell, Linda Bester, Malcolm Legg, Arthur Rylah Institute (ARI), Mornington Peninsula Shire, Russell Mawson, Bruce Fuhrer, Save Tootgarook Swamp, and Celine Yap. Maps: Mornington Peninsula Shire, Arthur Rylah Institute (ARI), and Practical Ecology. Further acknowledgements: This report was produced with the assistance and input of a number of ecological consultants, state agencies and Mornington Peninsula Shire community groups. The Shire is grateful to the many people that participated in the consultations and surveys informing this report. Acknowledgement of Country: The Mornington Peninsula Shire acknowledges Aboriginal and Torres Strait Islanders as the first Australians and recognises that they have a unique relationship with the land and water. The Shire also recognises the Mornington Peninsula is home to the Boonwurrung / Bunurong, members of the Kulin Nation, who have lived here for thousands of years and who have traditional connections and responsibilities to the land on which Council meets. Data sources - This booklet summarises the results of various biodiversity reports conducted for the Mornington Peninsula Shire: • Costen, A. and South, M. (2014) Tootgarook Wetland Ecological Character Description. Mornington Peninsula Shire. • Cook, D. (2013) Flora Survey and Weed Mapping at Tootgarook Swamp Bushland Reserve. Mornington Peninsula Shire. • Dell, M.D. and Bester L.R. (2006) Management and status of Leafy Greenhood (Pterostylis cucullata) populations within Mornington Peninsula Shire. Universal Ecology Services, Victoria. • Legg, M. (2014) Vertebrate fauna assessments of seven Mornington Peninsula Shire reserves located within Tootgarook Wetland. -
56. Otariidae and Phocidae
FAUNA of AUSTRALIA 56. OTARIIDAE AND PHOCIDAE JUDITH E. KING 1 Australian Sea-lion–Neophoca cinerea [G. Ross] Southern Elephant Seal–Mirounga leonina [G. Ross] Ross Seal, with pup–Ommatophoca rossii [J. Libke] Australian Sea-lion–Neophoca cinerea [G. Ross] Weddell Seal–Leptonychotes weddellii [P. Shaughnessy] New Zealand Fur-seal–Arctocephalus forsteri [G. Ross] Crab-eater Seal–Lobodon carcinophagus [P. Shaughnessy] 56. OTARIIDAE AND PHOCIDAE DEFINITION AND GENERAL DESCRIPTION Pinnipeds are aquatic carnivores. They differ from other mammals in their streamlined shape, reduction of pinnae and adaptation of both fore and hind feet to form flippers. In the skull, the orbits are enlarged, the lacrimal bones are absent or indistinct and there are never more than three upper and two lower incisors. The cheek teeth are nearly homodont and some conditions of the ear that are very distinctive (Repenning 1972). Both superfamilies of pinnipeds, Phocoidea and Otarioidea, are represented in Australian waters by a number of species (Table 56.1). The various superfamilies and families may be distinguished by important and/or easily observed characters (Table 56.2). King (1983b) provided more detailed lists and references. These and other differences between the above two groups are not regarded as being of great significance, especially as an undoubted fur seal (Australian Fur-seal Arctocephalus pusillus) is as big as some of the sea lions and has some characters of the skull, teeth and behaviour which are rather more like sea lions (Repenning, Peterson & Hubbs 1971; Warneke & Shaughnessy 1985). The Phocoidea includes the single Family Phocidae – the ‘true seals’, distinguished from the Otariidae by the absence of a pinna and by the position of the hind flippers (Fig.