The Diprotodons of Lake Callabonna
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SUPPLEMENTARY INFORMATION for a New Family of Diprotodontian Marsupials from the Latest Oligocene of Australia and the Evolution
Title A new family of diprotodontian marsupials from the latest Oligocene of Australia and the evolution of wombats, koalas, and their relatives (Vombatiformes) Authors Beck, RMD; Louys, J; Brewer, Philippa; Archer, M; Black, KH; Tedford, RH Date Submitted 2020-10-13 SUPPLEMENTARY INFORMATION FOR A new family of diprotodontian marsupials from the latest Oligocene of Australia and the evolution of wombats, koalas, and their relatives (Vombatiformes) Robin M. D. Beck1,2*, Julien Louys3, Philippa Brewer4, Michael Archer2, Karen H. Black2, Richard H. Tedford5 (deceased) 1Ecosystems and Environment Research Centre, School of Science, Engineering and Environment, University of Salford, Manchester, UK 2PANGEA Research Centre, School of Biological, Earth and Environmental Sciences, University of New South Wales, Sydney, New South Wales, Australia 3Australian Research Centre for Human Evolution, Environmental Futures Research Institute, Griffith University, Queensland, Australia 4Department of Earth Sciences, Natural History Museum, London, United Kingdom 5Division of Paleontology, American Museum of Natural History, New York, USA Correspondence and requests for materials should be addressed to R.M.D.B (email: [email protected]) This pdf includes: Supplementary figures Supplementary tables Comparative material Full description Relevance of Marada arcanum List of morphological characters Morphological matrix in NEXUS format Justification for body mass estimates References Figure S1. Rostrum of holotype and only known specimen of Mukupirna nambensis gen. et. sp. nov. (AMNH FM 102646) in ventromedial (a) and anteroventral (b) views. Abbreviations: C1a, upper canine alveolus; I1a, first upper incisor alveolus; I2a, second upper incisor alveolus; I1a, third upper incisor alveolus; P3, third upper premolar. Scale bar = 1 cm. -
Based on Comparative Morphological Data AF Emel'yanov Transactions of T
The phylogeny of the Cicadina (Homoptera, Cicadina) based on comparative morphological data A.F. Emel’yanov Transactions of the All-Union Entomological Society Morphological principles of insect phylogeny The phylogenetic relationships of the principal groups of cicadine* insects have been considered on more than one occasion, commencing with Osborn (1895). Some phylogenetic schemes have been based only on data relating to contemporary cicadines, i.e. predominantly on comparative morphological data (Kirkaldy, 1910; Pruthi, 1925; Spooner, 1939; Kramer, 1950; Evans, 1963; Qadri, 1967; Hamilton, 1981; Savinov, 1984a), while others have been constructed with consideration given to paleontological material (Handlirsch, 1908; Tillyard, 1919; Shcherbakov, 1984). As the most primitive group of the cicadines have been considered either the Fulgoroidea (Kirkaldy, 1910; Evans, 1963), mainly because they possess a small clypeus, or the cicadas (Osborn, 1895; Savinov, 1984), mainly because they do not jump. In some schemes even the monophyletism of the cicadines has been denied (Handlirsch, 1908; Pruthi, 1925; Spooner, 1939; Hamilton, 1981), or more precisely in these schemes the Sternorrhyncha were entirely or partially depicted between the Fulgoroidea and the other cicadines. In such schemes in which the Fulgoroidea were accepted as an independent group, among the remaining cicadines the cicadas were depicted as branching out first (Kirkaldy, 1910; Hamilton, 1981; Savinov, 1984a), while the Cercopoidea and Cicadelloidea separated out last, and in the most widely acknowledged systematic scheme of Evans (1946b**) the last two superfamilies, as the Cicadellomorpha, were contrasted to the Cicadomorpha and the Fulgoromorpha. At the present time, however, the view affirming the equivalence of the four contemporary superfamilies and the absence of a closer relationship between the Cercopoidea and Cicadelloidea (Evans, 1963; Emel’yanov, 1977) is gaining ground. -
Sound Radiation by the Bladder Cicada Cystosoma Saundersii
The Journal of Experimental Biology 201, 701–715 (1998) 701 Printed in Great Britain © The Company of Biologists Limited 1998 JEB1166 SOUND RADIATION BY THE BLADDER CICADA CYSTOSOMA SAUNDERSII H. C. BENNET-CLARK1,* AND D. YOUNG2 1Department of Zoology, Oxford University, South Parks Road, Oxford, OX1 3PS, UK and 2Department of Zoology, University of Melbourne, Parkville, Victoria 3052, Australia *e-mail: [email protected] Accepted 26 November 1997: published on WWW 5 February 1998 Summary Male Cystosoma saundersii have a distended thin-walled air sac volume was the major compliant element in the abdomen which is driven by the paired tymbals during resonant system. Increasing the mass of tergite 4 and sound production. The insect extends the abdomen from a sternites 4–6 also reduced the resonant frequency of the rest length of 32–34 mm to a length of 39–42 mm while abdomen. By extrapolation, it was shown that the effective singing. This is accomplished through specialised mass of tergites 3–5 was between 13 and 30 mg and that the apodemes at the anterior ends of abdominal segments 4–7, resonant frequency was proportional to 1/√(total mass), which cause each of these intersegmental membranes to suggesting that the masses of the tergal sound-radiating unfold by approximately 2 mm. areas were major elements in the resonant system. The calling song frequency is approximately 850 Hz. The The tymbal ribs buckle in sequence from posterior (rib song pulses have a bimodal envelope and a duration of 1) to anterior, producing a series of sound pulses. -
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. -
Megafauna Extinction
Episode 15 Teacher Resource 2nd June 2020 Megafauna Extinction 1. Before watching the BTN story, record what you know about Students will learn more about Australian megafauna and megafauna. investigate why they became 2. What is megafauna? extinct. 3. About how many years ago did megafauna exist in Australia? a. 4,000 b. 40,000 c. 400,000 Science – Year 6 The growth and survival of living 4. Complete the following sentence. A Diprotodon was a giant things are affected by physical _________________. conditions of their environment. 5. What did palaeontologist Dr Scott Hocknull and his team discover? Science – Year 7 6. Where did they make the discovery? Scientific knowledge has changed peoples’ understanding of the 7. What did they use to create images of what the megafauna might world and is refined as new have looked like? evidence becomes available. 8. Give some examples of the megafauna species they discovered. Interactions between organisms, 9. What might have caused megafauna to become extinct? including the effects of human 10. What did you learn watching the BTN story? activities can be represented by food chains and food webs. What do you know about megafauna? As a class discuss the BTN Megafauna Extinction story and ask students to record what they learnt watching the story. Record any questions they have. Here are some questions they can use to help guide their discussion. • What does the term megafauna mean? • When did megafauna exist? • How do we know they existed? • Why did megafauna grow so big? • What might have caused Australia’s megafauna to die out? Glossary Students will brainstorm a list of key words and terms that relate to the BTN Megafauna Extinction story. -
Chamber Music: an Unusual Helmholtz Resonator for Song Amplification in a Neotropical Bush-Cricket (Orthoptera, Tettigoniidae) Thorin Jonsson1,*, Benedict D
© 2017. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2017) 220, 2900-2907 doi:10.1242/jeb.160234 RESEARCH ARTICLE Chamber music: an unusual Helmholtz resonator for song amplification in a Neotropical bush-cricket (Orthoptera, Tettigoniidae) Thorin Jonsson1,*, Benedict D. Chivers1, Kate Robson Brown2, Fabio A. Sarria-S1, Matthew Walker1 and Fernando Montealegre-Z1,* ABSTRACT often a morphological challenge owing to the power and size of their Animals use sound for communication, with high-amplitude signals sound production mechanisms (Bennet-Clark, 1998; Prestwich, being selected for attracting mates or deterring rivals. High 1994). Many animals therefore produce sounds by coupling the amplitudes are attained by employing primary resonators in sound- initial sound-producing structures to mechanical resonators that producing structures to amplify the signal (e.g. avian syrinx). Some increase the amplitude of the generated sound at and around their species actively exploit acoustic properties of natural structures to resonant frequencies (Fletcher, 2007). This also serves to increase enhance signal transmission by using these as secondary resonators the sound radiating area, which increases impedance matching (e.g. tree-hole frogs). Male bush-crickets produce sound by tegminal between the structure and the surrounding medium (Bennet-Clark, stridulation and often use specialised wing areas as primary 2001). Common examples of these kinds of primary resonators are resonators. Interestingly, Acanthacara acuta, a Neotropical bush- the avian syrinx (Fletcher and Tarnopolsky, 1999) or the cicada cricket, exhibits an unusual pronotal inflation, forming a chamber tymbal (Bennet-Clark, 1999). In addition to primary resonators, covering the wings. It has been suggested that such pronotal some animals have developed morphological or behavioural chambers enhance amplitude and tuning of the signal by adaptations that act as secondary resonators, further amplifying constituting a (secondary) Helmholtz resonator. -
Relative Demographic Susceptibility Does Not Explain the Extinction Chronology of Sahul's Megafauna
bioRxiv preprint doi: https://doi.org/10.1101/2020.10.16.342303; this version posted October 19, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 1 Full title: Relative demographic susceptibility does not explain the 2 extinction chronology of Sahul’s megafauna 3 Short title: Demographic susceptibility of Sahul’s megafauna 4 5 Corey J. A. Bradshaw1,2,*, Christopher N. Johnson3,2, John Llewelyn1,2, Vera 6 Weisbecker4,2, Giovanni Strona5, and Frédérik Saltré1,2 7 1 Global Ecology, College of Science and Engineering, Flinders University, GPO Box 2100, Adelaide, 8 South Australia 5001, Australia, 2 ARC Centre of Excellence for Australian Biodiversity and Heritage, 9 EpicAustralia.org, 3 Dynamics of Eco-Evolutionary Pattern, University of Tasmania, Hobart, Tasmania 10 7001, Australia, 4 College of Science and Engineering, Flinders University, GPO Box 2100, Adelaide, 11 South Australia 5001, Australia, 5 Research Centre for Ecological Change, University of Helsinki, 12 Viikinkaari 1, Biocentre 3, 00790, Helsinki, Finland 13 14 * [email protected] (CJAB) 15 ORCIDs: C.J.A. Bradshaw: 0000-0002-5328-7741; C.N. Johnson: 0000-0002-9719-3771; J. 16 Llewelyn: 0000-0002-5379-5631; V. WeisbecKer: 0000-0003-2370-4046; F. Saltré: 0000- 17 0002-5040-3911 18 19 Keywords: vombatiformes, macropodiformes, flightless birds, carnivores, extinction 20 Author Contributions: C.J.A.B and F.S. conceptualized the paper, and C.J.A.B. -
An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna
© Copyright Australian Museum, 2005 Records of the Australian Museum (2005) Vol. 57: 375–446. ISSN 0067-1975 An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna M.S. MOULDS Australian Museum, 6 College Street, Sydney NSW 2010, Australia [email protected] ABSTRACT. The history of cicada family classification is reviewed and the current status of all previously proposed families and subfamilies summarized. All tribal rankings associated with the Australian fauna are similarly documented. A cladistic analysis of generic relationships has been used to test the validity of currently held views on family and subfamily groupings. The analysis has been based upon an exhaustive study of nymphal and adult morphology, including both external and internal adult structures, and the first comparative study of male and female internal reproductive systems is included. Only two families are justified, the Tettigarctidae and Cicadidae. The latter are here considered to comprise three subfamilies, the Cicadinae, Cicadettinae n.stat. (= Tibicininae auct.) and the Tettigadinae (encompassing the Tibicinini, Platypediidae and Tettigadidae). Of particular note is the transfer of Tibicina Amyot, the type genus of the subfamily Tibicininae, to the subfamily Tettigadinae. The subfamily Plautillinae (containing only the genus Plautilla) is now placed at tribal rank within the Cicadinae. The subtribe Ydiellaria is raised to tribal rank. The American genus Magicicada Davis, previously of the tribe Tibicinini, now falls within the Taphurini. Three new tribes are recognized within the Australian fauna, the Tamasini n.tribe to accommodate Tamasa Distant and Parnkalla Distant, Jassopsaltriini n.tribe to accommodate Jassopsaltria Ashton and Burbungini n.tribe to accommodate Burbunga Distant. -
Book of Abstracts Australian Mammal Society Conference 2020
BOOK OF ABSTRACTS Alphabetical author index on page 31 EASTERN GREY KANGAROO POPULATION DYNAMICS Rachel Bergeron1, David Forsyth2,3, Wendy King1,4 and Marco Festa-Bianchet1,4 1 Département de biologie, Université de Sherbrooke, Sherbrooke, Québec, J1K 2R1, Canada 2 Vertebrate Pest Research Unit, NSW Department of Primary Industries, Orange, NSW 2800, Australia 3 School of Biological, Earth and Environmental Sciences, University of New South Wales, Sydney, NSW 2052, Australia 4 School of Biological Sciences, Australian National University, Acton, ACT 2601, Australia Email: [email protected] Twitter: @festa_bianchet Recent studies of density-dependence in herbivore population dynamics seek to identify the mechanisms underlying these changes. Kangaroo populations experience large fluctuations in size. Early research suggested that rainfall was a good predictor of population changes through its effect on per capita food availability. Population dynamics of large herbivores, however, are likely influenced by interactions between stochastic environmental variation and density dependence. Vital rates can respond differently to environmental variation and to changes in density. In particular, juvenile survival is most sensitive to harsh conditions, and adult survival rarely affected. Consequently, an improved understanding of population dynamics requires monitoring of individuals of known sex and age under a variety of environmental conditions. I will investigate how density, age structure and environmental conditions affect the population dynamics of eastern grey kangaroos (Macropus giganteus) at Wilsons Promontory National Park, Victoria, where >1200 individuals of known age and sex have been monitored since 2008. I will test the hypothesis that environmental conditions and density dependence have interacting and age-specific roles in generating changes in population size. -
A New Family of Diprotodontian Marsupials from the Latest Oligocene of Australia and the Evolution of Wombats, Koalas, and Their Relatives (Vombatiformes) Robin M
www.nature.com/scientificreports OPEN A new family of diprotodontian marsupials from the latest Oligocene of Australia and the evolution of wombats, koalas, and their relatives (Vombatiformes) Robin M. D. Beck1,2 ✉ , Julien Louys3, Philippa Brewer4, Michael Archer2, Karen H. Black2 & Richard H. Tedford5,6 We describe the partial cranium and skeleton of a new diprotodontian marsupial from the late Oligocene (~26–25 Ma) Namba Formation of South Australia. This is one of the oldest Australian marsupial fossils known from an associated skeleton and it reveals previously unsuspected morphological diversity within Vombatiformes, the clade that includes wombats (Vombatidae), koalas (Phascolarctidae) and several extinct families. Several aspects of the skull and teeth of the new taxon, which we refer to a new family, are intermediate between members of the fossil family Wynyardiidae and wombats. Its postcranial skeleton exhibits features associated with scratch-digging, but it is unlikely to have been a true burrower. Body mass estimates based on postcranial dimensions range between 143 and 171 kg, suggesting that it was ~5 times larger than living wombats. Phylogenetic analysis based on 79 craniodental and 20 postcranial characters places the new taxon as sister to vombatids, with which it forms the superfamily Vombatoidea as defned here. It suggests that the highly derived vombatids evolved from wynyardiid-like ancestors, and that scratch-digging adaptations evolved in vombatoids prior to the appearance of the ever-growing (hypselodont) molars that are a characteristic feature of all post-Miocene vombatids. Ancestral state reconstructions on our preferred phylogeny suggest that bunolophodont molars are plesiomorphic for vombatiforms, with full lophodonty (characteristic of diprotodontoids) evolving from a selenodont morphology that was retained by phascolarctids and ilariids, and wynyardiids and vombatoids retaining an intermediate selenolophodont condition. -
1 TABLE S1 Global List of Extinct and Extant Megafaunal Genera By
Supplemental Material: Annu. Rev. Ecol. Syst.. 2006. 37:215-50 doi: 10.1146/annurev.ecolsys.34.011802.132415 Late Quaternary Extinctions: State of the Debate Koch and Barnosky TABLE S1 Global list of extinct and extant megafaunal genera by continent. STATUS TAXON TIME AFRICA Mammalia Carnivora Felidae Acinonyx Panthera Hyaenidae Crocuta Hyaena Ursidae Ursusa Primates Gorilla Proboscidea Elephantidae C Elephas <100 Loxodonta Perissodactyla Equidae S Equus <100 E Hipparion <100 Rhinocerotidae Ceratotherium Diceros E Stephanorhinus <100 Artiodactyla Bovidae Addax Ammotragus Antidorcas Alcelaphus Aepyceros C Bos 11.5-0 Capra Cephalopus Connochaetes Damaliscus Gazella S Hippotragus <100 Kobus E Rhynotragus/Megalotragus 11.5-0 Oryx E Pelorovis 11.5-0 E Parmulariusa <100 Redunca Sigmoceros Syncerus Taurotragus Tragelaphus Camelidae C Camelus <100 1 Supplemental Material: Annu. Rev. Ecol. Syst.. 2006. 37:215-50 doi: 10.1146/annurev.ecolsys.34.011802.132415 Late Quaternary Extinctions: State of the Debate Koch and Barnosky Cervidae E Megaceroides <100 Giraffidae S Giraffa <100 Okapia Hippopotamidae Hexaprotodon Hippopotamus Suidae Hylochoerus Phacochoerus Potamochoerus Susa Tubulidenta Orycteropus AUSTRALIA Reptilia Varanidae E Megalania 50-15.5 Meiolanidae E Meiolania 50-15.5 E Ninjemys <100 Crocodylidae E Palimnarchus 50-15.5 E Quinkana 50-15.5 Boiidae? E Wonambi 100-50 Aves E Genyornis 50-15.5 Mammalia Marsupialia Diprotodontidae E Diprotodon 50-15.5 E Euowenia <100 E Euryzygoma <100 E Nototherium <100 E Zygomaturus 100-50 Macropodidae S Macropus 100-50 E Procoptodon <100 E Protemnodon 50-15.5 E Simosthenurus 50-15.5 E Sthenurus 100-50 Palorchestidae E Palorchestes 50-15.5 Thylacoleonidae E Thylacoleo 50-15.5 Vombatidae S Lasiorhinus <100 E Phascolomys <100 E Phascolonus 50-15.5 E Ramsayia <100 2 Supplemental Material: Annu. -
Acoustics of Sound Production and of Hearing in the Bladder Cicada Cystosoma Saundersii (Westwood)
J. exp. Biol. (1978), 73, 43-55 43 With 8 figures Printed in Great Britain ACOUSTICS OF SOUND PRODUCTION AND OF HEARING IN THE BLADDER CICADA CYSTOSOMA SAUNDERSII (WESTWOOD) BY N. H. FLETCHER Department of Physics, University of New England, Armidale, N.S.W. 2351, Australia AND K. G. HILL Department of Neurobiology, Australian National University, Canberra, A.C.T. 2600, Australia (Received 17 May 1977) SUMMARY The male cicada of the species Cystosoma saundersii has a grossly enlarged, hollow abdomen and emits a loud calling song with a fundamental frequency of about 800 Hz. At the song frequency, its hearing is non- directional. The female of C. saundersii lacks sound producing organs, has no enlargement of the abdomen, but possesses an abdominal air sac and has well developed directional hearing at the frequency of the species' song. Physical mechanisms are proposed that explain these observations in semi-quantitative detail using the standard method of electrical network analogues. The abdomen in the male, with its enclosed air, is found to act as a system resonant at the song frequency, thus contributing a large gain in radiated sound intensity. Coupling between this resonator and the auditory tympana accounts for the observed hearing sensitivity in the male, but destroys directionality. In the female, the abdominal cavity acts in association with the two auditory tympana as part of a phase shift network which results in appreciable directionality of hearing at the unusually low frequency of the male song. INTRODUCTION The Australian bladder cicada Cystosoma saundersii (Westwood) is a remarkable insect in that the male produces a calling song which consists of a train of brief tone bursts of approximately 800 Hz sound repeated about 40 times per second.