Action Statement No.263
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Habitat Types
Habitat Types The following section features ten predominant habitat types on the West Coast of the Eyre Peninsula, South Australia. It provides a description of each habitat type and the native plant and fauna species that commonly occur there. The fauna species lists in this section are not limited to the species included in this publication and include other coastal fauna species. Fauna species included in this publication are printed in bold. Information is also provided on specific threats and reference sites for each habitat type. The habitat types presented are generally either characteristic of high-energy exposed coastline or low-energy sheltered coastline. Open sandy beaches, non-vegetated dunefields, coastal cliffs and cliff tops are all typically found along high energy, exposed coastline, while mangroves, sand flats and saltmarsh/samphire are characteristic of low energy, sheltered coastline. Habitat Types Coastal Dune Shrublands NATURAL DISTRIBUTION shrublands of larger vegetation occur on more stable dunes and Found throughout the coastal environment, from low beachfront cliff-top dunes with deep stable sand. Most large dune shrublands locations to elevated clifftops, wherever sand can accumulate. will be composed of a mosaic of transitional vegetation patches ranging from bare sand to dense shrub cover. DESCRIPTION This habitat type is associated with sandy coastal dunes occurring The understory generally consists of moderate to high diversity of along exposed and sometimes more sheltered coastline. Dunes are low shrubs, sedges and groundcovers. Understory diversity is often created by the deposition of dry sand particles from the beach by driven by the position and aspect of the dune slope. -
Phylogenetic Relationships of Terrestrial Australo-Papuan Elapid Snakes (Subfamily Hydrophiinae) Based on Cytochrome B and 16S Rrna Sequences J
MOLECULAR PHYLOGENETICS AND EVOLUTION Vol. 10, No. 1, August, pp. 67–81, 1998 ARTICLE NO. FY970471 Phylogenetic Relationships of Terrestrial Australo-Papuan Elapid Snakes (Subfamily Hydrophiinae) Based on Cytochrome b and 16S rRNA Sequences J. Scott Keogh,*,†,1 Richard Shine,* and Steve Donnellan† *School of Biological Sciences A08, University of Sydney, Sydney, New South Wales 2006, Australia; and †Evolutionary Biology Unit, South Australian Museum, North Terrace, Adelaide, South Australia 5000, Australia Received April 24, 1997; revised September 4, 1997 quence data support many of the conclusions reached Phylogenetic relationships among the venomous Aus- by earlier studies using other types of data, but addi- tralo-Papuan elapid snake radiation remain poorly tional information will be needed before the phylog- resolved, despite the application of diverse data sets. eny of the Australian elapids can be fully resolved. To examine phylogenetic relationships among this 1998 Academic Press enigmatic group, portions of the cytochrome b and 16S Key Words: mitochondrial DNA; cytochrome b; 16S rRNA mitochondrial DNA genes were sequenced from rRNA; reptile; snake; elapid; sea snake; Australia; New 19 of the 20 terrestrial Australian genera and 6 of the 7 Guinea; Pacific; Asia; biogeography. terrestrial Melanesian genera, plus a sea krait (Lati- cauda) and a true sea snake (Hydrelaps). These data clarify several significant issues in elapid phylogeny. First, Melanesian elapids form sister groups to Austra- INTRODUCTION lian species, indicating that the ancestors of the Austra- lian radiation came via Asia, rather than representing The diverse, cosmopolitan, and medically important a relict Gondwanan radiation. Second, the two major elapid snakes are a monophyletic clade of approxi- groups of sea snakes (sea kraits and true sea snakes) mately 300 species and 61 genera (Golay et al., 1993) represent independent invasions of the marine envi- primarily defined by their unique venom delivery sys- ronment. -
Frogs & Reptiles NE Vic 2018 Online
Reptiles and Frogs of North East Victoria An Identication and Conservation Guide Victorian Conservation Status (DELWP Advisory List) cr critically endangered en endangered Reptiles & Frogs vu vulnerable nt near threatened dd data deficient L Listed under the Flora and Fauna Guarantee Act (FFG, 1988) Size: of North East Victoria Lizards, Dragons & Skinks: Snout-vent length (cm) Snakes, Goannas: Total length (cm) An Identification and Conservation Guide Lowland Copperhead Highland Copperhead Carpet Python Gray's Blind Snake Nobbi Dragon Bearded Dragon Ragged Snake-eyed Skink Large Striped Skink Frogs: Snout-vent length male - M (mm) Snout-vent length female - F (mm) Austrelaps superbus 170 (NC) Austrelaps ramsayi 115 (PR) Morelia spilota metcalfei – en L 240 (DM) Ramphotyphlops nigrescens 38 (PR) Diporiphora nobbi 8.4 (PR) Pogona barbata – vu 25 (DM) Cryptoblepharus pannosus Snout-Vent 3.5 (DM) Ctenotus robustus Snout-Vent 12 (DM) Guide to symbols Venomous Lifeform F Fossorial (burrows underground) T Terrestrial Reptiles & Frogs SA Semi Arboreal R Rock-dwelling Habitat Type Alpine Bog Montane Forests Alpine Grassland/Woodland Lowland Grassland/Woodland White-lipped Snake Tiger Snake Woodland Blind Snake Olive Legless Lizard Mountain Dragon Marbled Gecko Copper-tailed Skink Alpine She-oak Skink Drysdalia coronoides 40 (PR) Notechis scutatus 200 (NC) Ramphotyphlops proximus – nt 50 (DM) Delma inornata 13 (DM) Rankinia diemensis Snout-Vent 7.5 (NC) Christinus marmoratus Snout-Vent 7 (PR) Ctenotus taeniolatus Snout-Vent 8 (DM) Cyclodomorphus praealtus -
Parasitic Worms in Reptiles from Tasmania and the Islands of Bass Strait
Papers and Proceedings of the Royal Society of Tasmania, Volume 137, 2003 7 PARASITIC WORMS IN REPTILES FROM TASMANIA AND THE ISLANDS OF BASS STRAIT by Hugh I. Jones (with two text-figures and one table) JONES, H.I., 2003 (19:xii): Parasitic worms in reptiles from Tasmania and the islands of Bass Strait. Papers and Proceedings of the Royal Society of Tasmania 137: 7-12. https://doi.org/10.26749/rstpp.137.7 ISSN 0080-4703. Department of Microbiology, University of Western Australia, Nedlands, Western Australia 6009, Australia. The endoparasitic worms in reptiles from Tasmania and the islands of Bass Strait were recorded from dissections of nine Tympanocryptis diemensis, six Tiliqua nigrolutea, 20 Cyclodomorphus casuarinae, 15 Egernia whitii, 17 Austreuzps superbus, 24 Notechis ater, seven Drysdalia coronoides and four Peuzmis platurus. Thirteen species of worms were recorded, namely, the pentastomes Waddycephalus superbus and Wad dycephalus ?sp. nov., an unidentified oxyurid nematode species, the nematodes Maxvachonia brygooi, M. chabaudi, Strongyluris paronai, Moaciria sp., Paraheterotyphlum australe, Ophidascaris pyrrhus, Kreisiella sp., Abbreviata antarctica, the trematode Dolichoperoides macalpini and the cestode Oochoristica vacuouzta. The roundworm 0. pyrrhus was most prevalent, occurring almost entirely in the Black Tiger Snake, N ater. The fluke D. macalpiniwas found, ofren at high intensity, in the Black Tiger Snake and in the Copperhead, A. superbus. No other worms occurred in more than two of any host species, and, apart from A. antarctica and 5. paronai, all nematodes were at an intensity of four or less worms per host. Six of the 13 helminth species were recovered only from the Bass Strait islands. -
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. -
Life History and Reproductive Variation in the Spotted Skink, Niveoscincus Ocellatus
Life History and Reproductive V ar ation in the Spotted S .. ink, Niveoscincus ocellatu_s (Gray 1845) T by Erik Wapstra BSc. (Hons) Life history variation · Niveoscincus ocella.tus Erik Wapstra "\ Declaration: This thesis contains no material which has been previously accepted for a degree or diploma by the University or any other institution, except by way of background information and duly acknowledged in the Thesis, and to the best of my knowledge and belief no material previously published or written by another person except where due acknowledgment is made in the text of the thesis. signed:~ , date: 'J-,.'3/;... /qg life history variation in Niveoscincus ocellatus Erik Wapstra This thesis may be made available for loan and limited copying in accordance with the Copyright Act 1968. Life history variation in Niveoscincus ocellatus Erik Wapstra Abstract Life history and reproductive variation in the spotted skink, Niveoscincus ocellatus The spotted skink, Niveoscincus ocellatus is a widely distributed small to medium size skink (3-12 g) which occurs throughout eastern and central Tasmania in a variety of climatic regimes. This thesis provides the first major ecological study of this species and describes in detail the life history and reproductive characteristics of two populations living at the climatic extremes of the species' distribution: a site on the Central Plateau represented the cold extreme and a site at Orford on the east coast represented the warm extreme. Niveoscincus ocellatus is a viviparous species that reproduces annually across its range. It shows an asynchronous gonadal cycle, with maximum male gonadal development in late summer and mating from April to June and August to September. -
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. https://doi.org/10.24199/j.mmv.1980.41.05 13 October 1980 TAXONOM1C REVISION OF THE ELAPID SNAKE GENUS DRYSDALIA WORRELL 1961 By A. J. Coventry* and P. A. RawunsonI * National Museum of Victoria, Russell Street, Melbourne, 3000. t Zoology Department, La Trobe University, Bundoora, 3083. Abstract The southern Australian snake genus Drysdalia (Worrell 1961) is reviewed and a key provided for the four species recognised. Drysdalia rhodogaster (Jan 1963) is elevated from synonymy and fully described for the first time. The types of each species are discussed in detail and lectotypes nominated where necessary. Introduction Drysdalia mastersii (Krefft, 1866) South Australia and adjacent areas Boulenger (1896) allocated many of the small Southern in Australia and Victoria. Australian elapid snakes to the genus Denisonia Western Krefft, 1869. Australian herpetologists followed Drysdalia rhodogaster (Jan, 1863) Boulenger's scheme until the genus Denisonia South-eastern New South Wales. unwieldy, polyphyletic taxon. For became an As there is an extensive literature on example, Kinghorn (1956) listed 19 (27-5%) of venomous snakes, mainly for the popular the 69 Australian elapid species and subspecies market, only publications considered to be of under this genus. In 1961 Worrell revised the primary taxonomic importance have been in- the previously genus Denisonia and re-allocated cluded in the synonymies. included species to ten genera, eight of which he Abbreviations used for institutions in this revision described for the first time. Worrell's paper are: proved controversial and some of his alloca- Australian Museum AM tions were not accepted. Cogger (1979) presents British Museum (Natural History) BM(NH) consensus view of the accepted taxa. -
Rangelands, Western Australia
Biodiversity Summary for NRM Regions Species List What is the summary for and where does it come from? This list has been produced by the Department of Sustainability, Environment, Water, Population and Communities (SEWPC) for the Natural Resource Management Spatial Information System. The list was produced using the AustralianAustralian Natural Natural Heritage Heritage Assessment Assessment Tool Tool (ANHAT), which analyses data from a range of plant and animal surveys and collections from across Australia to automatically generate a report for each NRM region. Data sources (Appendix 2) include national and state herbaria, museums, state governments, CSIRO, Birds Australia and a range of surveys conducted by or for DEWHA. For each family of plant and animal covered by ANHAT (Appendix 1), this document gives the number of species in the country and how many of them are found in the region. It also identifies species listed as Vulnerable, Critically Endangered, Endangered or Conservation Dependent under the EPBC Act. A biodiversity summary for this region is also available. For more information please see: www.environment.gov.au/heritage/anhat/index.html Limitations • ANHAT currently contains information on the distribution of over 30,000 Australian taxa. This includes all mammals, birds, reptiles, frogs and fish, 137 families of vascular plants (over 15,000 species) and a range of invertebrate groups. Groups notnot yet yet covered covered in inANHAT ANHAT are notnot included included in in the the list. list. • The data used come from authoritative sources, but they are not perfect. All species names have been confirmed as valid species names, but it is not possible to confirm all species locations. -
Supplementary Methods S1
1 Validation methods for trophic niche models 2 3 To assign links between nodes (species), we used trophic niche-space models (e.g., [1]). 4 Each of these models has two quantile regressions that define the prey-size range a 5 predator of a given size is predicted to consume. Species whose body mass is within the 6 range of a predator’s prey size, as identified by the trophic niche-space model, are predicted 7 to be prey, while those outside the range are predicted not to be eaten. 8 9 The broad taxonomy of a predator helps to predict predation interactions [2]. To optimize 10 our trophic niche-space model, we therefore tested whether including taxonomic class of 11 predators improved the fit of quantile regressions. Using trophic (to identify which species 12 were predators), body mass, and taxonomic data, we fitted and compared five quantile 13 regression models (including a null model) to the GloBI data. In each model, we log10- 14 transformed the dependent variable prey body mass, and included for the independent 15 variables different combinations of log10-transformed predator body mass, predator class, 16 and the interaction between these variables (Supplementary Table S4). We log10- 17 transformed both predator and prey body mass to linearize the relationship between these 18 variables. We fit the five quantile regressions to the upper and lower 5% of prey body mass, 19 and compared model fits using the Bayesian information criterion (BIC). The predator body 20 mass*predator class model fit the 95th quantile data best, whereas the predator body mass 21 + predator class model fit the 5th quantile data marginally better than the aforementioned 22 interaction model (Supplementary Figure S2, Supplementary Table S4). -
WABN #170 2019 Jun.Pdf
Western Australian Bird Notes Quarterly Newsletter of the Western Australian Branch of BirdLife Australia No. 170 June 2019 birds are in our nature Figure 6a. Google Earth map of the Western Lease, Dampier Saltworks and (below) Figure 6b. Google Earth map of the Eastern Lease, Dampier Saltworks (see report, pages 17-19) See report, page 20. Figure 1. Months in which Hooded Plover flocks larger than 100 were recorded (1982-2019). Front cover: Fairy Tern, Rous Head Fremantle. Photo by Claire Greenwell (see report, page 4) Page 2 Western Australian Bird Notes, No. 170 June 2019 Western Australian Branch of ExECuTiVE COMMittee, 2019 BirdLife Australia Office: Peregrine House Chair: Mr Viv Read 167 Perry Lakes Drive, Floreat WA 6014 Vice Chair: Dr Mike Bamford Hours: Monday-Friday 9:30 am to 12.30 pm Telephone: (08) 9383 7749 Secretary: Lou Scampoli E-mail: [email protected] Treasurer: Beverly Winterton BirdLife WA web page: www.birdlife.org.au/wa Chair: Mr Viv Read Committee: Alasdair Bulloch, Max Goodwin, Mark Henryon, Andrew Hobbs, Jennifer Sumpton and one vacancy (due to BirdLife Western Australia is the WA Branch of the national resignation of Plaxy Barratt) organisation, BirdLife Australia. We are dedicated to creating a brighter future for Australian birds. General meetings: Held at the Bold Park Eco Centre, Perry Lakes Drive, Floreat, commencing 7:30 pm on the 4th Monday of the month (except December) – see ‘Coming events’ for details. Executive meetings: Held at Peregrine House on the 2nd Monday of the month. Communicate any matters for consideration to the Chair. Western Australian Bird Notes Print ISSN 1445-3983 Online ISSN 2206-8716 Joint WABN Editors: Allan Burbidge Tel: (08) 9405 5109 (w) Tel/Fax: (08) 9306 1642 (h) Fax: (08) 9306 1641 (w) E-mail: [email protected] Suzanne Mather Tel: (08) 9389 6416 E-mail: [email protected] Production: Margaret Philippson Printing and distribution: Daniels Printing Craftsmen Tel: (08) 9204 6800 danielspc.com.au Notes for Contributors Red-throated Pipit, Meekatharra (see Observations, page 11). -
Relationship of Old World Pseudoxenodon and New World Dipsadinae, with Comments on Underestimation of Species Diversity of Chinese Pseudoxenodon
Asian Herpetological Research 2013, 4(3): 155–165 DOI: 10.3724/SP.J.1245.2013.00155 Relationship of Old World Pseudoxenodon and New World Dipsadinae, with Comments on Underestimation of Species Diversity of Chinese Pseudoxenodon Baolin ZHANG1, 2, 3 and Song HUANG1, 3, 4* 1 College of Life and Environment Sciences, Huangshan University, Huangshan 245021, Anhui, China 2 School of Life Sciences, Yunnan University, Kunming 650091, Yunnan, China 3 State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, Yunnan, China 4 Institute of Biodiversity and Geobiology, Department of Life Sciences, Tibet University, Lhasa 850000, Tibet, China Abstract Assessment of the relationship between Pseudoxenodon and Dipsadinae has been hampered by lack of adequate samples. In this paper, we conducted phylogenetic analyses using two mitochondrial genes (12S and 16S rRNA) and one nuclear gene (c-mos) from thirteen specimens representing two species of Pseudoxenodon, together with 84 sequences of caenophidians and an outgroup sequence of Boa constrictor. Our study suggests that the Southeast Asian genus, Pseudoxenodon forms a robust genetic subclade within South American xenodontines, indicating that at least one lineage within this genus entered or returned to the Old World (OW) from the New World (NW) across the Beringian Land Bridge during the early Tertiary and the warm mid-Miocene. It also reveals the high intraspecific genomic variation within the populations of Pseudoxenodon macrops, indicating that species diversity of Pseudoxenodon in China is likely underestimated. Keywords phylogenetic position, 12S rRNA, 16S rRNA, Beringian Land Bridge, cryptic species 1. Introduction includes approximately 3000 species of extant snakes (Lawson et al., 2005; Vidal et al., 2007). -
Habitat Restoration and Management of Endangered Species on Sydney Sandstone Outcrops
Habitat Restoration and Management of Endangered Species on Sydney Sandstone Outcrops Benjamin Michael Croak A thesis submitted in fulfilment of the requirements for the degree of Doctor of Philosophy School of Biological Sciences THE UNIVERSITY OE SYDNEY September 2012 Declaration I hereby certify that the work presented in this thesis is my own (except where specifically acknowledged), and that this thesis has not been used to attain a degree at another university. Preface In accordance with current practice at The University of Sydney, this thesis is presented as a series of stand-alone manuscripts that have either been submitted to international journals for peer review, or have been peer reviewed and accepted for publication. Because they are similarly themed stand-alone manuscripts, there is some unavoidable repetition. Most of the ideas contained in this thesis are my own. In other cases I contributed substantially to the development of ideas, and the majority of work (including planning, designing, implementing, analysing and writing of manuscripts) was undertaken by me under the guidance of my supervisors. To maintain transparency regarding the level of contribution, I have listed all co-authors as they appear in published articles. Due to joint- authorship, the work presented in most chapters is discussed as “we” instead of “I”. All work was conducted under the approval of the Animal Ethics Committee of The University of Sydney (Animal ethics permit number: L04/12-2008/3/4927) and was approved by New South Wales National Parks and Wildlife Service (NPWS Scientific Licence: SL100472). Acknowledgements My project would not have been possible without the input of a large group of people who have assisted, encouraged, listened to, volunteered for and generally helped me throughout my candidature.