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Life History of the Coppertail Skink (Ctenotus Taeniolatus) in Southeastern Australia
Herpetological Conservation and Biology 15(2):409–415. Submitted: 11 February 2020; Accepted: 19 May 2020; Published: 31 August 2020. LIFE HISTORY OF THE COPPERTAIL SKINK (CTENOTUS TAENIOLATUS) IN SOUTHEASTERN AUSTRALIA DAVID A. PIKE1,2,6, ELIZABETH A. ROZNIK3, JONATHAN K. WEBB4, AND RICHARD SHINE1,5 1School of Biological Sciences A08, University of Sydney, New South Wales 2006, Australia 2Present address: Department of Biology, Rhodes College, Memphis, Tennessee 38112, USA 3Department of Conservation and Research, Memphis Zoo, Memphis, Tennessee 38112, USA 4School of Life Sciences, University of Technology Sydney, Broadway, New South Wales 2007, Australia 5Present address: Department of Biological Sciences, Macquarie University, New South Wales 2109, Australia 6Corresponding author, e-mail: [email protected] Abstract.—The global decline of reptiles is a serious problem, but we still know little about the life histories of most species, making it difficult to predict which species are most vulnerable to environmental change and why they may be vulnerable. Life history can help dictate resilience in the face of decline, and therefore understanding attributes such as sexual size dimorphism, site fidelity, and survival rates are essential. Australia is well-known for its diversity of scincid lizards, but we have little detailed knowledge of the life histories of individual scincid species. To examine the life history of the Coppertail Skink (Ctenotus taeniolatus), which uses scattered surface rocks as shelter, we estimated survival rates, growth rates, and age at maturity during a three-year capture-mark- recapture study. We captured mostly females (> 84%), and of individuals captured more than once, we captured 54.3% at least twice beneath the same rock, and of those, 64% were always beneath the same rock (up to five captures). -
An Intial Estimation of the Numbers and Identification of Extant Non
Answers Research Journal 8 (2015):171–186. www.answersingenesis.org/arj/v8/lizard-kinds-order-squamata.pdf $Q,QLWLDO(VWLPDWLRQRIWKH1XPEHUVDQG,GHQWLÀFDWLRQRI Extant Non-Snake/Non-Amphisbaenian Lizard Kinds: Order Squamata Tom Hennigan, Truett-McConnell College, Cleveland, Georgia. $EVWUDFW %LRV\VWHPDWLFVLVLQJUHDWÁX[WRGD\EHFDXVHRIWKHSOHWKRUDRIJHQHWLFUHVHDUFKZKLFKFRQWLQXDOO\ UHGHÀQHVKRZZHSHUFHLYHUHODWLRQVKLSVEHWZHHQRUJDQLVPV'HVSLWHWKHODUJHDPRXQWRIGDWDEHLQJ SXEOLVKHGWKHFKDOOHQJHLVKDYLQJHQRXJKNQRZOHGJHDERXWJHQHWLFVWRGUDZFRQFOXVLRQVUHJDUGLQJ WKHELRORJLFDOKLVWRU\RIRUJDQLVPVDQGWKHLUWD[RQRP\&RQVHTXHQWO\WKHELRV\VWHPDWLFVIRUPRVWWD[D LVLQJUHDWIOX[DQGQRWZLWKRXWFRQWURYHUV\E\SUDFWLWLRQHUVLQWKHILHOG7KHUHIRUHWKLVSUHOLPLQDU\SDSHU LVmeant to produce a current summary of lizard systematics, as it is understood today. It is meant to lay a JURXQGZRUNIRUFUHDWLRQV\VWHPDWLFVZLWKWKHJRDORIHVWLPDWLQJWKHQXPEHURIEDUDPLQVEURXJKWRQ WKH $UN %DVHG RQ WKH DQDO\VHV RI FXUUHQW PROHFXODU GDWD WD[RQRP\ K\EULGL]DWLRQ FDSDELOLW\ DQG VWDWLVWLFDO EDUDPLQRORJ\ RI H[WDQW RUJDQLVPV D WHQWDWLYH HVWLPDWH RI H[WDQW QRQVQDNH QRQ DPSKLVEDHQLDQOL]DUGNLQGVZHUHWDNHQRQERDUGWKH$UN,WLVKRSHGWKDWWKLVSDSHUZLOOHQFRXUDJH IXWXUHUHVHDUFKLQWRFUHDWLRQLVWELRV\VWHPDWLFV Keywords: $UN(QFRXQWHUELRV\VWHPDWLFVWD[RQRP\UHSWLOHVVTXDPDWDNLQGEDUDPLQRORJ\OL]DUG ,QWURGXFWLRQ today may change tomorrow, depending on the data Creation research is guided by God’s Word, which and assumptions about that data. For example, LVIRXQGDWLRQDOWRWKHVFLHQWLÀFPRGHOVWKDWDUHEXLOW naturalists assume randomness and universal 7KHELEOLFDODQGVFLHQWLÀFFKDOOHQJHLVWRLQYHVWLJDWH -
Level 2 Fauna Survey MEELUP REGIONAL PARK
Level 2 Fauna Survey MEELUP REGIONAL PARK APRIL 2015 suite 1, 216 carp st (po box 470) bega nsw 2550 australia t (02) 6492 8333 www.nghenvironmental.com.au e [email protected] unit 18, level 3, 21 mary st suite 1, 39 fitzmaurice st (po box 5464) surry hills nsw 2010 australia wagga wagga nsw 2650 australia t (02) 8202 8333 t (02) 6971 9696 unit 17, 27 yallourn st (po box 62) room 15, 341 havannah st (po box 434) fyshwick act 2609 australia bathurst nsw 2795 australia t (02) 6280 5053 0488 820 748 Document Verification Project Title: MEELUP REGIONAL PARK Project Number: 5354 Project File Name: Meelup Regional Park Level 2 Fauna Survey v20150115 Revision Date Prepared by (name) Reviewed by (name) Approved by (name) DRAFT 27/03/15 Shane Priddle Nick Graham-Higgs Nick Graham-Higgs (SW Environmental) and Greg Harewood Final 17/04/15 Shane Priddle Shane Priddle Shane Priddle (SW Environmental) (SW Environmental) (SW Environmental) nghenvironmental prints all documents on environmentally sustainable paper including paper made from bagasse (a by- product of sugar production) or recycled paper. nghenvironmental is a registered trading name of NGH Environmental Pty Ltd; ACN: 124 444 622. ABN: 31 124 444 622 suite 1, 216 carp st (po box 470) bega nsw 2550 australia t (02) 6492 8333 www.nghenvironmental.com.au e [email protected] unit 18, level 3, 21 mary st suite 1, 39 fitzmaurice st (po box 5464) surry hills nsw 2010 australia wagga wagga nsw 2650 australia t (02) 8202 8333 t (02) 6971 9696 unit 17, 27 yallourn st (po box 62) room 15, 341 havannah st (po box 434) fyshwick act 2609 australia bathurst nsw 2795 australia t (02) 6280 5053 0488 820 748 Level 2 Fauna Survey MEELUP REGIONAL PARK CONTENTS LEVEL 2 FAUNA SURVEY ..................................................................................................................... -
Three New Species of Ctenotus (Reptilia: Sauria: Scincidae)
DOI: 10.18195/issn.0312-3162.25(2).2009.181-199 Records of the Western Australian Museum 25: 181–199 (2009). Three new species of Ctenotus (Reptilia: Sauria: Scincidae) from the Kimberley region of Western Australia, with comments on the status of Ctenotus decaneurus yampiensis Paul Horner Museum and Art Gallery of the Northern Territory, GPO Box 4646, Darwin, Northern Territory 0801, Australia. E-mail: [email protected] Abstract – Three new species of Ctenotus Storr, 1964 (Reptilia: Sauria: Scinci- dae), C. halysis sp. nov., C. mesotes sp. nov. and C. vagus sp. nov. are described. Previously confused with C. decaneurus Storr, 1970 or C. alacer Storr, 1970, C. halysis sp. nov. and C. vagus sp. nov. are members of the C. atlas species com- plex. Ctenotus mesotes sp. nov. was previously confused with C. tantillus Storr, 1975 and is a member of the C. schomburgkii species complex. The new taxa are terrestrial, occurring in woodland habitats on sandy soils in the Kimberley region of Western Australia and are distinguished from congeners by combi- nations of body patterns, mensural and meristic characteristics. Comments are provided on the taxonomic status of C. yampiensis Storr, 1975 which is considered, as in the original description, a subspecies of C. decaneurus. Re- descriptions of C. d. decaneurus and C. d. yampiensis are provided. Keywords – Ctenotus alacer, decaneurus, yampiensis, halysis, mesotes, tantillus, vagus, morphology, new species, Kimberley region, Western Australia INTRODUCTION by combinations of size, scale characteristics, body Ctenotus Storr, 1964 is the most species-rich genus colour and patterns. of scincid lizards in Australia, with almost 100 taxa recognised (Horner 2007; Wilson and Swan 2008). -
Mitochondrial Introgression Via Ancient Hybridization, and Systematics of the Australian Endemic Pygopodid Gecko Genus Delma Q ⇑ Ian G
Molecular Phylogenetics and Evolution 94 (2016) 577–590 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Mitochondrial introgression via ancient hybridization, and systematics of the Australian endemic pygopodid gecko genus Delma q ⇑ Ian G. Brennan , Aaron M. Bauer, Todd R. Jackman Department of Biology, Villanova University, 800 Lancaster Avenue, Villanova, PA 19085, USA article info abstract Article history: Of the more than 1500 species of geckos found across six continents, few remain as unfamiliar as the Received 11 May 2015 pygopodids – Family Pygopodidae (Gray, 1845). These gekkotans are limited to Australia (44 species) Revised 21 September 2015 and New Guinea (2 species), but have diverged extensively into the most ecologically diverse limbless Accepted 6 October 2015 radiation save Serpentes. Current phylogenetic understanding of the family has relied almost exclusively Available online 23 October 2015 on two works, which have produced and synthesized an immense amount of morphological, geograph- ical, and molecular data. However, current interspecific relationships within the largest genus Delma Gray Keywords: 1831 are based chiefly upon data from two mitochondrial loci (16s, ND2). Here, we reevaluate the inter- Mitochondrial capture specific relationships within the genus Delma using two mitochondrial and four nuclear loci (RAG1, Introgression Biogeography MXRA5, MOS, DYNLL1), and identify points of strong conflict between nuclear and mitochondrial geno- Pygopodidae mic data. We address mito-nuclear discordance, and remedy this conflict by recognizing several points of Gekkota mitochondrial introgression as the result of ancient hybridization events. Owing to the legacy value and intraspecific informativeness, we suggest the continued use of ND2 as a phylogenetic marker. -
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 -
Catalogue of Protozoan Parasites Recorded in Australia Peter J. O
1 CATALOGUE OF PROTOZOAN PARASITES RECORDED IN AUSTRALIA PETER J. O’DONOGHUE & ROBERT D. ADLARD O’Donoghue, P.J. & Adlard, R.D. 2000 02 29: Catalogue of protozoan parasites recorded in Australia. Memoirs of the Queensland Museum 45(1):1-164. Brisbane. ISSN 0079-8835. Published reports of protozoan species from Australian animals have been compiled into a host- parasite checklist, a parasite-host checklist and a cross-referenced bibliography. Protozoa listed include parasites, commensals and symbionts but free-living species have been excluded. Over 590 protozoan species are listed including amoebae, flagellates, ciliates and ‘sporozoa’ (the latter comprising apicomplexans, microsporans, myxozoans, haplosporidians and paramyxeans). Organisms are recorded in association with some 520 hosts including mammals, marsupials, birds, reptiles, amphibians, fish and invertebrates. Information has been abstracted from over 1,270 scientific publications predating 1999 and all records include taxonomic authorities, synonyms, common names, sites of infection within hosts and geographic locations. Protozoa, parasite checklist, host checklist, bibliography, Australia. Peter J. O’Donoghue, Department of Microbiology and Parasitology, The University of Queensland, St Lucia 4072, Australia; Robert D. Adlard, Protozoa Section, Queensland Museum, PO Box 3300, South Brisbane 4101, Australia; 31 January 2000. CONTENTS the literature for reports relevant to contemporary studies. Such problems could be avoided if all previous HOST-PARASITE CHECKLIST 5 records were consolidated into a single database. Most Mammals 5 researchers currently avail themselves of various Reptiles 21 electronic database and abstracting services but none Amphibians 26 include literature published earlier than 1985 and not all Birds 34 journal titles are covered in their databases. Fish 44 Invertebrates 54 Several catalogues of parasites in Australian PARASITE-HOST CHECKLIST 63 hosts have previously been published. -
Pentastomiasis in Australian Re
Fact sheet Pentastomiasis (also known as Porocephalosis) is a disease caused by infection with pentastomids. Pentastomids are endoparasites of vertebrates, maturing primarily in the respiratory system of carnivorous reptiles (90% of all pentastomid species), but also in toads, birds and mammals. Pentastomids have zoonotic potential although no human cases have been reported in Australia. These parasites have an indirect life cycle involving one or more intermediate host. They may be distinguished from other parasite taxa by the presence of four hooks surrounding their mouth, which they use for attaching to respiratory tissue to feed on host blood. Pentastomid infections are often asymptomatic, but adult and larval pentastomids can cause severe pathology resulting in the death of their intermediate and definitive hosts, usually via obstruction of airways or secondary bacterial and/or fungal infections. Pentastomiasis in reptiles is caused by endoparasitic metazoans of the subclass Pentastomida. Four genera are known to infect crocodiles in Australia: Alofia, Leiperia, Sebekia, and Selfia; all in the family Sebekidae. Three genera infect lizards in Australia: Raillietiella (Family: Raillietiellidae), Waddycephalus (Family: Sambonidae) and Elenia (Family: Sambonidae). Four genera infect snakes in Australia: Waddycephalus, Parasambonia (Family: Sambonidae), Raillietiella and Armillifer (Family: Armilliferidae). Definitive hosts Many species of Australian reptiles, including snakes, lizards and crocodiles are proven definitive hosts for pentastomes (see Appendix 1). Lizards may be both intermediate and definitive hosts for pentastomids. Raillietiella spp. occurs primarily in small to medium-sized lizards and Elenia australis infects large varanids. Nymphs of Waddycephalus in several lizard species likely reflect incidental infection; it is possible that lizards are an intermediate host for Waddycephalus. -
Biodiversity Summary: Port Phillip and Westernport, Victoria
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. -
NSW Native Animal Keepers' Species List 2014
NSW Native Animal Keepers’ Species List 2014 The NSW Native Animal Keepers’ Species List 2014 (also available at www.environment.nsw.gov.au) contains the names of all species that may be kept under licence. If the animal species you want to keep isn’t listed, you generally cannot keep it, although the Department might consider requests to keep unlisted species of reptile, bird or amphibian. If you are applying for a licence for an unlisted species, you will need to supply details of the species and numbers you are proposing to keep, the legal availability of the species and its husbandry requirements in captivity. A new species list is produced by the Department each year. You can only hold an animal that is applicable to class as listed in the current year’s species list. Some animals are listed as exempt and a licence is not required to hold or trade those species (see exempt species list at the back of this document). Some hybridised animals are recorded in this list. The Department does not support native animal keepers who breed between animals of different species. Regulations prohibit the breeding of native waterfowl with domestic waterfowl. Your licence must be endorsed with the class under which the species is applicable. Holding requirements for venomous reptiles must be in accordance with the requirements contained in the class criteria for advanced reptile venomous category 1,2 or 3 as contained in the “Application for an Advanced Class- Native Animal Keepers’ Licence.” If you acquire or dispose of a native species of Cockatoo listed as applicable to class B1, or any species of animal listed under A2,B2,B3,R2,R3,R4 or R5 you must notify the Director General by email or in writing of the details of the transaction within fourteen days of the transaction taking place. -
Reptiles and Frogs of Gluepot Reserve (Updated June 2020)
Reptiles and Frogs of Gluepot Reserve (updated June 2020) Scientific name Common name Notes with reference to Gluepot Family Agamidae Dragon Lizards Ctenophorus spinodomus1 Eastern Mallee Dragon Terrestrial, associated with spinifex, commonly observed Ctenophorus pictus Painted Dragon Terrestrial, commonly observed Diporiphora nobbi Nobbi Dragon Terrestrial/arboreal, commonly observed Pogona vitticeps Central Bearded Dragon Terrestrial, commonly observed Family Gekkonidae Typical Geckos Gehyra versicolor2 Eastern Tree Dtella Arboreal, nocturnal, commonly observed on buildings Heteronotia binoei Bynoe’s Gecko Terrestrial, nocturnal, occasionally observed Family Carphodactylidae Knob-tails & others Nephrurus levis Smooth Knob-tailed Gecko Terrestrial, nocturnal, occasionally observed Family Diplodactylidae Diplodactylus furcosis Ranges Stone Gecko Terrestrial, nocturnal, occasionally observed Diplodactylus vittatus Eastern Stone Gecko Terrestrial, nocturnal, occasionally observed Lucasium damaeum Beaded Gecko Terrestrial, nocturnal, commonly observed Oedura cincta3 Inland Marbled Velvet Gecko Arboreal, nocturnal, on Black Oak, rarely observed Rhynchoedura angusta4 Border Beaked Gecko Terrestrial, nocturnal, occasionally observed. Strophurus elderi Jewelled Gecko Terrestrial, nocturnal, in spinifex, occasionally observed Strophurus williamsi Eastern Spiny-tailed Gecko Terrestrial/arboreal, nocturnal, occasionally observed Family Pygopodidae Legless Lizards Aprasia inaurita Red-tailed Worm Lizard Terrestrial, rarely observed, often under -
(Reptilia: Squamata: Scincidae) Species Group and a New Species of Immediate Conservation Concern in the Southwestern Australian Biodiversity Hotspot
Zootaxa 3390: 1–18 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2012 · Magnolia Press ISSN 1175-5334 (online edition) Molecular phylogeny and morphological revision of the Ctenotus labillardieri (Reptilia: Squamata: Scincidae) species group and a new species of immediate conservation concern in the southwestern Australian biodiversity hotspot GEOFFREY M. KAY & J. SCOTT KEOGH 1 Division of Evolution, Ecology and Genetics, Research School of Biology, The Australian National University, Canberra, ACT 0200, Australia 1 Corresponding author. E-mail: [email protected] Abstract Ctenotus is the largest and most diverse genus of skinks in Australia with at least 97 described species. We generated large mitochondrial and nuclear DNA data sets for 70 individuals representing all available species in the C. labillardieri species- group to produce the first comprehensive phylogeny for this clade. The widespread C. labillardieri was sampled extensively to provide the first detailed phylogeographic data set for a reptile in the southwestern Australian biodiversity hotspot. We supplemented our molecular data with a comprehensive morphological dataset for the entire group, and together these data are used to revise the group and describe a new species. The morphologically highly variable species C. labillardieri comprises seven well-supported genetic clades that each occupy distinct geographic regions. The phylogeographic patterns observed in this taxon are consistent with studies of frogs, plants and invertebrates, adding strength to emerging biogeographic hypotheses in this iconic region. The species C. catenifer, C. youngsoni, and C. gemmula are well supported, and despite limited sampling both C. catenifer and C. gemmula show substantial genetic structure.