Lerista Desertorum – a New Skink Species for Queensland with Notes
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Integrative and Comparative Biology Integrative and Comparative Biology, Volume 60, Number 1, Pp
Integrative and Comparative Biology Integrative and Comparative Biology, volume 60, number 1, pp. 190–201 doi:10.1093/icb/icaa015 Society for Integrative and Comparative Biology SYMPOSIUM Convergent Evolution of Elongate Forms in Craniates and of Locomotion in Elongate Squamate Reptiles Downloaded from https://academic.oup.com/icb/article-abstract/60/1/190/5813730 by Clark University user on 24 July 2020 Philip J. Bergmann ,* Sara D. W. Mann,* Gen Morinaga,1,*,† Elyse S. Freitas‡ and Cameron D. Siler‡ *Department of Biology, Clark University, Worcester, MA, USA; †Department of Integrative Biology, Oklahoma State University, Stillwater, OK, USA; ‡Department of Biology and Sam Noble Oklahoma Museum of Natural History, University of Oklahoma, Norman, OK, USA From the symposium “Long Limbless Locomotors: The Mechanics and Biology of Elongate, Limbless Vertebrate Locomotion” presented at the annual meeting of the Society for Integrative and Comparative Biology January 3–7, 2020 at Austin, Texas. 1E-mail: [email protected] Synopsis Elongate, snake- or eel-like, body forms have evolved convergently many times in most major lineages of vertebrates. Despite studies of various clades with elongate species, we still lack an understanding of their evolutionary dynamics and distribution on the vertebrate tree of life. We also do not know whether this convergence in body form coincides with convergence at other biological levels. Here, we present the first craniate-wide analysis of how many times elongate body forms have evolved, as well as rates of its evolution and reversion to a non-elongate form. We then focus on five convergently elongate squamate species and test if they converged in vertebral number and shape, as well as their locomotor performance and kinematics. -
Phylogenetic Structure of Vertebrate Communities Across the Australian
Journal of Biogeography (J. Biogeogr.) (2013) 40, 1059–1070 ORIGINAL Phylogenetic structure of vertebrate ARTICLE communities across the Australian arid zone Hayley C. Lanier*, Danielle L. Edwards and L. Lacey Knowles Department of Ecology and Evolutionary ABSTRACT Biology, Museum of Zoology, University of Aim To understand the relative importance of ecological and historical factors Michigan, Ann Arbor, MI 48109-1079, USA in structuring terrestrial vertebrate assemblages across the Australian arid zone, and to contrast patterns of community phylogenetic structure at a continental scale. Location Australia. Methods We present evidence from six lineages of terrestrial vertebrates (five lizard clades and one clade of marsupial mice) that have diversified in arid and semi-arid Australia across 37 biogeographical regions. Measures of within-line- age community phylogenetic structure and species turnover were computed to examine how patterns differ across the continent and between taxonomic groups. These results were examined in relation to climatic and historical fac- tors, which are thought to play a role in community phylogenetic structure. Analyses using a novel sliding-window approach confirm the generality of pro- cesses structuring the assemblages of the Australian arid zone at different spa- tial scales. Results Phylogenetic structure differed greatly across taxonomic groups. Although these lineages have radiated within the same biome – the Australian arid zone – they exhibit markedly different community structure at the regio- nal and local levels. Neither current climatic factors nor historical habitat sta- bility resulted in a uniform response across communities. Rather, historical and biogeographical aspects of community composition (i.e. local lineage per- sistence and diversification histories) appeared to be more important in explaining the variation in phylogenetic structure. -
Fowlers Gap Biodiversity Checklist Reptiles
Fowlers Gap Biodiversity Checklist ow if there are so many lizards then they should make tasty N meals for someone. Many of the lizard-eaters come from their Reptiles own kind, especially the snake-like legless lizards and the snakes themselves. The former are completely harmless to people but the latter should be left alone and assumed to be venomous. Even so it odern reptiles are at the most diverse in the tropics and the is quite safe to watch a snake from a distance but some like the Md rylands of the world. The Australian arid zone has some of the Mulga Snake can be curious and this could get a little most diverse reptile communities found anywhere. In and around a disconcerting! single tussock of spinifex in the western deserts you could find 18 species of lizards. Fowlers Gap does not have any spinifex but even he most common lizards that you will encounter are the large so you do not have to go far to see reptiles in the warmer weather. Tand ubiquitous Shingleback and Central Bearded Dragon. The diversity here is as astonishing as anywhere. Imagine finding six They both have a tendency to use roads for passage, warming up or species of geckos ranging from 50-85 mm long, all within the same for display. So please slow your vehicle down and then take evasive genus. Or think about a similar diversity of striped skinks from 45-75 action to spare them from becoming a road casualty. The mm long! How do all these lizards make a living in such a dry and Shingleback is often seen alone but actually is monogamous and seemingly unproductive landscape? pairs for life. -
Morphological and Molecular Assessment of Aprasia Fusca and A
RECORDS OF THE WESTERN AUSTRALIAN MUSEUM 28 144–163 (2013) Morphological and molecular assessment of Aprasia fusca and A. rostrata (Squamata: Pygopodidae), with a description of a new species from the Lake MacLeod region, Western Australia Brad Maryan¹,4, Brian G. Bush² and Mark Adams³ ¹ Biologic Environmental Survey, 50B Angove Street, North Perth, Western Australia 6006, Australia. Email: [email protected] ² Snakes Harmful and Harmless, 9 Birch Place, Stoneville, Western Australia 6554, Australia. ³ Evolutionary Biology Unit, South Australian Museum, North Terrace, Adelaide, South Australia 5000, Australia. 4 Department of Terrestrial Zoology, Western Australian Museum, 49 Kew Street, Welshpool, Western Australia 6106, Australia. ABSTRACT – The Australian pygopodid genus Aprasia comprises a group of small, morphologically conservative, worm-like fossorial lizards, many of which are distributed along the west coast of the continent. This study re-examines the taxonomic distinctiveness of the two most northerly occurring species in Western Australia: A. fusca and A. rostrata, which are very similar in morphology. A combined morphological and allozyme analysis revealed these two species to be conspecifi c with A. rostrata considered a senior synonym of A. fusca. As a consequence, we have redescribed A. rostrata. The allozyme analysis also revealed a new species, named here as Aprasia litorea sp. nov. This species occurs in the Lake Macleod region, well to the south of its congener, A. rostrata, and the two species are diagnosable using a conservative suite of morphological and meristic characters. KEYWORDS: worm lizard, synonymy, Aprasia litorea sp. nov., North West Cape, Montebello Islands, Barrow Island, allozyme electrophoresis INTRODUCTION the fi rst British atomic weapons (Hill 1955). -
Evolution of Limblessness
Evolution of Limblessness Evolution of Limblessness Early on in life, many people learn that lizards have four limbs whereas snakes have none. This dichotomy not only is inaccurate but also hides an exciting story of repeated evolution that is only now beginning to be understood. In fact, snakes represent only one of many natural evolutionary experiments in lizard limblessness. A similar story is also played out, though to a much smaller extent, in amphibians. The repeated evolution of snakelike tetrapods is one of the most striking examples of parallel evolution in animals. This entry discusses the evolution of limblessness in both reptiles and amphibians, with an emphasis on the living reptiles. Reptiles Based on current evidence (Wiens, Brandley, and Reeder 2006), an elongate, limb-reduced, snakelike morphology has evolved at least twenty-five times in squamates (the group containing lizards and snakes), with snakes representing only one such origin. These origins are scattered across the evolutionary tree of squamates, but they seem especially frequent in certain families. In particular, the skinks (Scincidae) contain at least half of all known origins of snakelike squamates. But many more origins within the skink family will likely be revealed as the branches of their evolutionary tree are fully resolved, given that many genera contain a range of body forms (from fully limbed to limbless) and may include multiple origins of snakelike morphology as yet unknown. These multiple origins of snakelike morphology are superficially similar in having reduced limbs and an elongate body form, but many are surprisingly different in their ecology and morphology. This multitude of snakelike lineages can be divided into two ecomorphs (a are surprisingly different in their ecology and morphology. -
Front Matter
Cambridge University Press 978-1-107-03044-2 - How the Snake Lost Its Legs: Curious Tales from the Frontier of Evo-Devo Lewis I. Held Frontmatter More information How the Snake Lost its Legs Curious Tales from the Frontier of Evo-Devo How did the zebra really get its stripes, and the giraffe its long neck? What is the science behind camel humps, leopard spots, and other animal oddities? Such questions have fascinated us for centuries, but the expanding field of evo-devo (evolutionary developmental biology) is now providing, for the first time, a wealth of insights and answers. Taking inspiration from Kipling’s Just So Stories, this book weaves emerging insights from evo-devo into a narrative that provides startling explanations for the origin and evolution of traits across the animal kingdom. The author’s unique and engaging style makes this narrative both enlightening and entertaining, guiding students and researchers through even complex concepts and encouraging a fuller understanding of the latest developments in the field. The first five chapters cover the first bilaterally symmetric animals, flies, butterflies, snakes, and cheetahs. A final chapter surveys recent results about a menagerie of other animals. Lewis I. Held, Jr. is Associate Professor of Biology at Texas Tech University, Lubbock, Texas, USA. He has taught developmental biology and human embryology to pre- medical students for twenty-seven years, and received the 2010 Professing Excellence Award and the 1995 President’s Excellence in Teaching Medal (Texas Tech University). He is also the author of Quirks of Human Anatomy (Cambridge, 2009), Imaginal Discs (Cambridge, 2002), and Models for Embryonic Periodicity (Karger, 1992). -
A Phylogeny and Revised Classification of Squamata, Including 4161 Species of Lizards and Snakes
BMC Evolutionary Biology This Provisional PDF corresponds to the article as it appeared upon acceptance. Fully formatted PDF and full text (HTML) versions will be made available soon. A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes BMC Evolutionary Biology 2013, 13:93 doi:10.1186/1471-2148-13-93 Robert Alexander Pyron ([email protected]) Frank T Burbrink ([email protected]) John J Wiens ([email protected]) ISSN 1471-2148 Article type Research article Submission date 30 January 2013 Acceptance date 19 March 2013 Publication date 29 April 2013 Article URL http://www.biomedcentral.com/1471-2148/13/93 Like all articles in BMC journals, this peer-reviewed article can be downloaded, printed and distributed freely for any purposes (see copyright notice below). Articles in BMC journals are listed in PubMed and archived at PubMed Central. For information about publishing your research in BMC journals or any BioMed Central journal, go to http://www.biomedcentral.com/info/authors/ © 2013 Pyron et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes Robert Alexander Pyron 1* * Corresponding author Email: [email protected] Frank T Burbrink 2,3 Email: [email protected] John J Wiens 4 Email: [email protected] 1 Department of Biological Sciences, The George Washington University, 2023 G St. -
A LIST of the VERTEBRATES of SOUTH AUSTRALIA
A LIST of the VERTEBRATES of SOUTH AUSTRALIA updates. for Edition 4th Editors See A.C. Robinson K.D. Casperson Biological Survey and Research Heritage and Biodiversity Division Department for Environment and Heritage, South Australia M.N. Hutchinson South Australian Museum Department of Transport, Urban Planning and the Arts, South Australia 2000 i EDITORS A.C. Robinson & K.D. Casperson, Biological Survey and Research, Biological Survey and Research, Heritage and Biodiversity Division, Department for Environment and Heritage. G.P.O. Box 1047, Adelaide, SA, 5001 M.N. Hutchinson, Curator of Reptiles and Amphibians South Australian Museum, Department of Transport, Urban Planning and the Arts. GPO Box 234, Adelaide, SA 5001updates. for CARTOGRAPHY AND DESIGN Biological Survey & Research, Heritage and Biodiversity Division, Department for Environment and Heritage Edition Department for Environment and Heritage 2000 4thISBN 0 7308 5890 1 First Edition (edited by H.J. Aslin) published 1985 Second Edition (edited by C.H.S. Watts) published 1990 Third Edition (edited bySee A.C. Robinson, M.N. Hutchinson, and K.D. Casperson) published 2000 Cover Photograph: Clockwise:- Western Pygmy Possum, Cercartetus concinnus (Photo A. Robinson), Smooth Knob-tailed Gecko, Nephrurus levis (Photo A. Robinson), Painted Frog, Neobatrachus pictus (Photo A. Robinson), Desert Goby, Chlamydogobius eremius (Photo N. Armstrong),Osprey, Pandion haliaetus (Photo A. Robinson) ii _______________________________________________________________________________________ CONTENTS -
Ord Victoria Plains 1
Ord Victoria Plains 1 Ord Victoria Plains 1 (OVP1 – Ord subregion) GORDON GRAHAM AUGUST 2001 Information from Western Australia and the Northern Territory has been listed separately in this synopsis as a result of different vegetation mapping protocols that have been used in the two jurisdictions and the associated difficulties in combining that information. Subregional description and biodiversity bitextura (curly spinifex) hummock grassland wooded with Eucalyptus spp or Bauhinia values cunninghamii (bauhinia) low trees. • Eucalyptus pruinosa (silver box) +/- Bauhinia Description and area cunninghamii (bauhinia) low open-woodland +/- a shrub layer and tussock grasses or Triodia spp. Western Australia: (spinifex) • The bioregion shows level to gently undulating plains Eucalyptus spp. grassy woodland • with scattered hills on Cambrian volcanics and Eucalyptus terminalis (desert bloodwood) low open- Proterozoic sedimentary rocks; vertosols on plains and woodland with Sehima nervosum (white grass) and predominantly skeletal soils on hills. The overall Chrysopogon fallax (golden beard grass) tussock vegetation is grassland with scattered bloodwoods grasses +/- Triodia spp. (spinifex). • (Eucalyptus spp.) and snappy gum (Eucalyptus brevifolia) Eucalyptus opaca (plains bloodwood) and Eucalyptus with spinifex and annual grasses. The climate is dry hot chlorophylla (shiny-leaved box) sparse low-open tropical, semi-arid with summer rainfall. The subregional woodland with tussock grasses or a Triodia pungens area is 2, 282, 600ha. (soft spinifex), Triodia intermedia (winged spinifex) hummock grassland wooded with Eucalyptus The lithological mosaic has three main components: brevifolia. (1) Abrupt Proterozoic and Phanerozoic ranges and • Triodia wiseana (limestone spinifex) open-hummock scattered hills mantled by shallow sand and loam grassland wooded with low trees of Terminalia spp. -
Reptiles on the Brink: Identifying the Australian Terrestrial Snake and Lizard Species Most at Risk of Extinction
CSIRO PUBLISHING Pacific Conservation Biology, 2021, 27, 3–12 https://doi.org/10.1071/PC20033 Reptiles on the brink: identifying the Australian terrestrial snake and lizard species most at risk of extinction Hayley M. Geyle A, Reid Tingley B, Andrew P. AmeyC, Hal CoggerD, Patrick J. CouperC, Mark CowanE, Michael D. CraigF,G, Paul DoughtyH, Don A. DriscollI, Ryan J. EllisH,J, Jon-Paul EmeryF, Aaron FennerK, Michael G. GardnerK,L, Stephen T. Garnett A, Graeme R. GillespieM, Matthew J. GreenleesN, Conrad J. HoskinO, J. Scott KeoghP, Ray LloydQ, Jane Melville R, Peter J. McDonaldS, Damian R. MichaelT, Nicola J. Mitchell F, Chris SandersonU,V, Glenn M. Shea W,X, Joanna Sumner R, Erik WapstraY, John C. Z. Woinarski A and David G. Chapple B,Z AThreatened Species Recovery Hub, National Environmental Science Program, Research Institute for the Environment and Livelihoods, Charles Darwin University, NT 0909, Australia. BSchool of Biological Sciences, Monash University, Clayton, Vic. 3800, Australia. CBiodiversity Program, Queensland Museum, South Brisbane, Qld 4101, Australia. DAustralian Museum, Sydney, NSW 2010, Australia. EDepartment of Biodiversity, Conservation and Attractions, Kensington, WA 6151, Australia. FSchool of Biological Sciences, The University of Western Australia, Crawley, WA 6009, Australia. GSchool of Veterinary and Life Sciences, Murdoch University, Murdoch, WA 6150, Australia. HDepartment of Terrestrial Zoology, Western Australian Museum, Welshpool, WA 6106, Australia. ICentre for Integrative Ecology, School of Life and Environmental Sciences, Deakin University, Burwood, Vic. 3125, Australia. JBiologic Environmental Survey, East Perth, WA 6004, Australia. KCollege of Science and Engineering, Flinders University, Bedford Park, SA 5042, Australia. LEvolutionary Biology Unit, South Australian Museum, Adelaide, SA 5000, Australia. -
Environmental Heritage & Social Impact Services
OCTOBER 2012 ENVIRONMENTAL HERITAGE & SOCIAL IMPACT SERVICES THUNDERBIRD DAMPIER PENINSULA PROJECT CULTURAL HERITAGE FLORA AND FAUNA ASSESSMENT REPORT TO THE KIMBERLEY LAND COUNCIL ABORIGINAL CORPORATION & THE NATIVE TITLE CLAIM GROUP This page has been left blank intentionally ENVIRONMENTAL HERITAGE & SOCIAL IMPACT SERVICES THUNDERBIRD DAMPIER PENINSULA PROJECT CULTURAL HERITAGE FLORA AND FAUNA ASSESSMENT REPORT TO THE KIMBERLEY LAND COUNCIL ABORIGINAL CORPORATION & THE NATIVE TITLE CLAIM GROUP Kimberley Land Council Aboriginal Corporation and the Native Title Claim Group Thunderbird Dampier Peninsula Project Cultural Heritage Flora and Fauna Assessment Document Status Approved for Issue Rev. Author Reviewer/s Date Name Distributed To Date 1 R. Young R. Young 29/08/12 L. Roque-Albelo M. Powers 31/08/12 N. Jackett M. Fairborn J Graff 2 N. Jackett K. Honczar 22/10/12 K. Honczar M. Powers 23/10/12 ecologia Environment (2012). Reproduction of this report in whole or in part by electronic, mechanical or chemical means including photocopying, recording or by any information storage and retrieval system, in any language, is strictly prohibited without the express approval of the Kimberley Land Council Aboriginal Corporation, the Native Title Claim Group and/or ecologia Environment. Restrictions on Use This report has been prepared specifically for the Kimberley Land Council Aboroginal Corporation and the Native Title Claim Group. Neither the report nor its contents may be referred to or quoted in any statement, study, report, application, prospectus, loan, or other agreement document (with the exception of when this document is required to be publicly released as part of a statutory approval process), without the express approval of the Kimberley Land Council Aboroginal Corporation and the Native Title Claim Group and/or ecologia Environment. -
The Taxonomic Status of Lerista Aericeps Storr 1986 with a Diagnosis of the Lerista Orientalis Species Group
Rc( Hi'\! \11<1 1990, J4(41 441,44X The taxonomic status of Lerista aericeps Storr 1986 with a diagnosis of the Lerista orientalis species group. Allen L Greer* Abstract {.crista aericeps aericeps Storr. 19116 IS shown to be a Junior synonym of Lerisla xall/hum Storr. 1976, La, laeniala Storr. 19116 is a distinct species, The L oriell/atis species group. of which these species are members. is diagnosed and a key to the species of Jhe group IS presented, Introduction Lerista aericeps was recently described as a new species with two subspecies: L. a. aericeps from the southeastern Northern Territory and southwestern Queensland and L a. taeniata from the central western Northern Territory (Storr 1986). This taxonomic arrangement created a unique situation in Lerista: two distinctly patterned forms in one specIes a plai n form (aericeps) and a strongly laterally stri ped form (taeniata). Upon examining this situation, a different taxonomic arrangement became evident which appears to resolve the colour pattern anomaly. This new taxonomic arrangement is presented here in the slightly larger context of the Lerista orienta/is species group to which these species appear to belong. The Lerista orientalis Species Group The Lerista orienta/is species group consists of four species and may be diagnosed vis-a-vis all other Lerista (Greer 1986) on the basis of the following derived characters: supraoculars three; pretemporals fused; supraciliaries five, third and fourth interdigitating with supraoculars; spectacle present; size small (maximum SVL =53mm); supralabials six; phalangeal formula 0.2.3.4.2/0.2.3.5.3. (or less), and presacral vertebrae 2: 35.