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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). -
Reptiles of the Wet Tropics
Reptiles of the Wet Tropics The concentration of endemic reptiles in the Wet Tropics is greater than in any other area of Australia. About 162 species of reptiles live in this region and 24 of these species live exclusively in the rainforest. Eighteen of them are found nowhere else in the world. Many lizards are closely related to species in New Guinea and South-East Asia. The ancestors of two of the resident geckos are thought to date back millions of years to the ancient super continent of Gondwana. PRICKLY FOREST SKINK - Gnypetoscincus queenlandiae Length to 17cm. This skink is distinguished by its very prickly back scales. It is very hard to see, as it is nocturnal and hides under rotting logs and is extremely heat sensitive. Located in the rainforest in the Wet Tropics only, from near Cooktown to west of Cardwell. RAINFOREST SKINK - Eulamprus tigrinus Length to 16cm. The body has irregular, broken black bars. They give birth to live young and feed on invertebrates. Predominantly arboreal, they bask in patches of sunlight in the rainforest and shelter in tree hollows at night. Apparently capable of producing a sharp squeak when handled or when fighting. It is rare and found only in rainforests from south of Cooktown to west of Cardwell. NORTHERN RED-THROATED SKINK - Carlia rubrigularis Length to 14cm. The sides of the neck are richly flushed with red in breeding males. Lays 1-2 eggs per clutch, sometimes communally. Forages for insects in leaf litter, fallen logs and tree buttresses. May also prey on small skinks and own species. -
Literature Cited in Lizards Natural History Database
Literature Cited in Lizards Natural History database Abdala, C. S., A. S. Quinteros, and R. E. Espinoza. 2008. Two new species of Liolaemus (Iguania: Liolaemidae) from the puna of northwestern Argentina. Herpetologica 64:458-471. Abdala, C. S., D. Baldo, R. A. Juárez, and R. E. Espinoza. 2016. The first parthenogenetic pleurodont Iguanian: a new all-female Liolaemus (Squamata: Liolaemidae) from western Argentina. Copeia 104:487-497. Abdala, C. S., J. C. Acosta, M. R. Cabrera, H. J. Villaviciencio, and J. Marinero. 2009. A new Andean Liolaemus of the L. montanus series (Squamata: Iguania: Liolaemidae) from western Argentina. South American Journal of Herpetology 4:91-102. Abdala, C. S., J. L. Acosta, J. C. Acosta, B. B. Alvarez, F. Arias, L. J. Avila, . S. M. Zalba. 2012. Categorización del estado de conservación de las lagartijas y anfisbenas de la República Argentina. Cuadernos de Herpetologia 26 (Suppl. 1):215-248. Abell, A. J. 1999. Male-female spacing patterns in the lizard, Sceloporus virgatus. Amphibia-Reptilia 20:185-194. Abts, M. L. 1987. Environment and variation in life history traits of the Chuckwalla, Sauromalus obesus. Ecological Monographs 57:215-232. Achaval, F., and A. Olmos. 2003. Anfibios y reptiles del Uruguay. Montevideo, Uruguay: Facultad de Ciencias. Achaval, F., and A. Olmos. 2007. Anfibio y reptiles del Uruguay, 3rd edn. Montevideo, Uruguay: Serie Fauna 1. Ackermann, T. 2006. Schreibers Glatkopfleguan Leiocephalus schreibersii. Munich, Germany: Natur und Tier. Ackley, J. W., P. J. Muelleman, R. E. Carter, R. W. Henderson, and R. Powell. 2009. A rapid assessment of herpetofaunal diversity in variously altered habitats on Dominica. -
IMPACTS of the UNPRECEDENTED 2019-20 BUSHFIRES on AUSTRALIAN ANIMALS NOVEMBER 2020 Acknowledgements
AUSTRALIA IMPACTS OF THE UNPRECEDENTED 2019-20 BUSHFIRES ON AUSTRALIAN ANIMALS NOVEMBER 2020 Acknowledgements WWF-Australia acknowledges the Traditional Owners of the land on which we work and their continuing connection to their lands, waters, and culture. We pay our respects to Elders – past and present, and their emerging leaders. WWF-Australia is part of the world’s largest conservation network. WWF-Australia has been working to create a world where people live in harmony with nature since 1978. WWF’s mission is to stop the degradation of the Earth’s CONTENTS natural environment and to build a future in which humans live in harmony with nature, by conserving the world’s biological diversity, ensuring that the use of renewable natural resources is sustainable, and promoting the EXECUTIVE SUMMARY 6 reduction of pollution and wasteful consumption. Prepared by Lily M van Eeden, Dale Nimmo, Michael BACKGROUND 10 Mahony, Kerryn Herman, Glenn Ehmke, Joris Driessen, James O’Connor, Gilad Bino, Martin Taylor and Chris 1.1 Fire in Australia 10 Dickman for WWF-Australia 1.2 The 2019-20 bushfire season 10 We are grateful to the researchers who provided data or feedback on the report. These include: 1.3 Scope of this study 12 • Eddy Cannella 1.3.1 Taxa included 14 • David Chapple 1.3.2 Study area 14 • Hugh Davies • Deanna Duffy 1.4 Limitations 17 • Hugh Ford • Chris Johnson 1. MAMMALS 18 • Brad Law 2.1 Methods 18 • Sarah Legge • David Lindenmayer 2.1.1 Most mammals 18 • Simon McDonald 2.1.2 Koalas 19 • Damian Michael 2.2 Results 22 • Harry Moore • Stewart Nichol 2.3 Caveats 22 • Alyson Stobo-Wilson • Reid Tingley 2. -
ASH Newsletter 46 2011 Print.Pub
THE AUSTRALIAN SOCIETY OF HERPETOLOGISTS INCORPORATED NEWSLETTER 46 2 History of Office Bearers Formation Committee (April 1964):- MJ Littlejohn (Convenor); State Reps IR Straughan (Qld), FJ Mitchell (SA), HG Cogger (NSW), G Storr (WA), RE Barw ick (ACT), JW Warren (Vic), AK Lee (Editor). First AGM (23 August 1965):- President MJ Littlejohn, Vice-President NG Stephenson, Sec- retary-Treasurer AA Martin, Asst Secretary-Treasurer KJ Wilson, Ordinary Members FJ Mitchell and IR Straughan, Editor AK Lee. PRESIDENT:- MJ Littlejohn (1965-69); AK Lee (1969-70); HG Cogger (1971-73); J de Bavay (1974); H Heatw ole (1975-76); GC Grigg (1976-77); MJ Tyler (1978-79); GF Watson (1979- 81); AA Martin (1981-82); RS Seymour (1982-83); R Shine (1983-84); GC Grigg (1984-86); J Coventry (1986-87); RE Barw ick (1987-88); J Covacevich (1988-91); M Davies (1991-92); R Shine (1992-94); A Georges (1994-6); D Roberts (1996-98); M Bull (1998-9); R Swain (1999- 2001); S Dow nes (2001-03); J Melville (2004-2005); J-M Hero (2005-2007); P Doherty (2007- 2008); M Thompson (2008-2009); M Hutchinson (2009-2010); L Schwarzkopf (2010-) VICE-PRESIDENT:- NG Stephenson (1965-67); RE Barw ick (1967-69); HG Cogger (1969- 70); MJ Littlejohn (1971-72); MJ Tyler (1973); HG Cogger (1974); J de Bavay (1975-76); H Heatw ole (1976-77); GC Grigg (1977-79); MJ Tyler (1979-80); GF Watson (1981-82); AA Martin (1982-83); RS Seymour (1983-84); R Shine (1984-86); GC Grigg (1986-87); J Coventry (1987-88); RE Barw ick (1988-91); J Covacevich (1991-92); M Davies (1992-94); R Shine (1994-6); A Georges (1996-98); D Roberts (1998-99); M Bull(1999-2001); R Sw ain (2001- 2003); S Dow nes (2004-5); J Melville (2005-2007); J-M Hero (2007-2008); P Doherty (2008- 2009); M Thompson (2009-2010); M Hutchinson (2010-) SECRETARY/TREASURER:- AA Martin (1965-67); GF Watson (1967-72); LA Moffatt (1973- 75); J Caughley (19375-76); RWG Jenkins (1976-77); M Davies (1978-83); G Courtice (1983- 87); J Wombey (1987-99); S Keogh (1999-2003); N Mitchell (2004-5); E. -
Accessory Publication Table S1. the Percentage of Pregnant Female Lizards Reported As Failing to Give Birth to Any Viable Offspr
10.1071/RD9195_AC © CSIRO 2010 Accessory Publication: Reproduction Fertility and Development, 2010, 22(5), 761–770. Accessory Publication Table S1. The percentage of pregnant female lizards reported as failing to give birth to any viable offspring when housed experimentally under seemingly favourable conditions for that species (see literature cited; i.e. individuals within studies that had no added stressors, such as hormone injections, and where dams were exposed to thermal regimes providing the greatest pregnancy success) Stage refers to the embryonic stage of pregnancy at which lizards were captured: E = early pregnant; L = late-pregnant (see text for rationale behind stage of pregnancy). Type refers to the embryonic nutritional support provided (references in brackets): I = predominantly lecithotrophic with type I chorioallantoic placenta; II = type II chorioallantoic placenta; III = type III chorioallantoic placenta; IV = type IV chorioallantoic placenta (microlecithal eggs). ND = no data (pregnancy status not stated/type of placentation unknown) Family Stage Type % failure Literature cited Species (N females) Diplodactylidae Hoplodactylus maculatus (common gecko) L I 12% (9) Cree et al. 2003; unpub. obs. (Girling et al. 1997) Naultinus manukanus (Marlborough green gecko) L ND 0% (10) Hare et al. 2007 Family Stage Type % failure Literature cited Species (N females) Iguanidae Sceloporus jarrovi (Yarrow’s spiny lizard) ND I 10% (10) Beuchat 1988 (D. G. Blackburn, pers. comm.) S. jarrovi (Yarrow’s spiny lizard) L I 0% (15) Mathies and Andrews 1997 (D. G. Blackburn, pers. comm.) Lacertidae Lacerta (Zootoca) vivipara ND I 25% (56) Uller and Olsson 2003 (Stewart et al. 2004) Lacerta (Zootoca) vivipara ND I 0% (5) Van Damme et al. -
A Predictive Framework and Review of the Ecological Impacts of Exotic Plant Invasions on Reptiles and Amphibians
A predictive framework and review of the ecological impacts of exotic plant invasions on reptiles and amphibians Leigh J. Martin* and Brad R. Murray Plant Functional Biology and Climate Change Cluster, Department of Environmental Sciences, University of Technology Sydney, PO Box 123, Broadway, NSW 2007, Australia *Author for correspondence (Tel: + 61 2 9514 8346; Fax: + 61 2 9514 4079; E-mail: [email protected]). 2 ABSTRACT The invasive spread of exotic plants in native vegetation can pose serious threats to native faunal assemblages. This is of particular concern for reptiles and amphibians because they form a significant component of the world’s vertebrate fauna, play a pivotal role in ecosystem functioning and are often neglected in biodiversity research. A framework to predict how exotic plant invasion will affect reptile and amphibian assemblages is imperative for conservation, management and the identification of research priorities. Here, we present a new predictive framework that integrates three mechanistic models. These models are based on exotic plant invasion altering: (1) habitat structure; (2) herbivory and predator-prey interactions; (3) the reproductive success of reptile and amphibian species and assemblages. We present a series of testable predictions from these models that arise from the interplay over time among three exotic plant traits (growth form, area of coverage, taxonomic distinctiveness) and six traits of reptiles and amphibians (body size, lifespan, home range size, habitat specialisation, diet, reproductive strategy). A literature review provided robust empirical evidence of exotic plant impacts on reptiles and amphibians from each of the three model mechanisms. Evidence relating to the role of body size and diet was less clear-cut, indicating the need for further research. -
Vocalisation and Aggression in the Prickly Forest Skink Gnypetoscincus Queenslandiae
Vocalisation and aggression in the Prickly Forest Skink Gnypetoscincus queenslandiae Dave O’Connor School of Biological Sciences, University of Sydney, NSW 2006, Australia. [email protected] Key words: Aggression, vocalisation, scincidae, territoriality, Prickly Forest Skink Downloaded from http://meridian.allenpress.com/australian-zoologist/article-pdf/32/2/265/1475730/az_2003_010.pdf by guest on 28 September 2021 Introduction Vocalisation is an important component of territorial containers (20 x 27 cm) for a period of approximately a displays in a number of taxonomic groups including birds, year before the current observations. The contents of the mammals, fishes, reptiles and amphibians (e.g. Nelson terrarium were designed to mimic the natural environment 1984; Fernandez-Juricic et al. 1999; Myrberg 1997; of the lizards ie. moist soil substrate, limited vegetation Marcellini 1977; Ovaska and Caldbeck 1997). Territorial and two small hollow logs as shelter/basking sites. advertising using calls is hypothesised to reduce Observations were made indoors under a combination of antagonistic interactions, thereby conserving energy and natural and artificial (UV) light . reducing the risk of combat induced injuries. Whilst Within five minutes of the animals first being placed territorial behaviour has been widely documented, the together in the enclosure they were observed alongside majority of observations are biased towards males due to each other, head to tail. One skink, the “aggressor”, was their larger size and/or more evident displays (Mahrt making a series of high pitched squeaks. After 1998; Stamps 1977). approximately ten seconds of vocalisation the aggressor Aside from geckos there have been very few observations of then bit at the tail of the “subordinate”. -
Queensland Environmental Offsets Policy Version 1.10
Queensland Environmental Offsets Policy Page 1 of 68 • EPP/2021/1658 • Version 1.10 • Last Reviewed: 03/03/2021 Department of Environment and Science Page 1 of 68 • EPP/2021/1658 • Version 1.10 • Last Reviewed: 03/03/2021 Department of Environment and Science Prepared by: Conservation Policy and Planning, Department of Environment and Science © State of Queensland, 2021. The Queensland Government supports and encourages the dissemination and exchange of its information. The copyright in this publication is licensed under a Creative Commons Attribution 3.0 Australia (CC BY) licence. Under this licence you are free, without having to seek our permission, to use this publication in accordance with the licence terms. You must keep intact the copyright notice and attribute the State of Queensland as the source of the publication. For more information on this licence, visit http://creativecommons.org/licenses/by/3.0/au/deed.en Disclaimer While this document has been prepared with care it contains general information and does not profess to offer legal, professional or commercial advice. The Queensland Government accepts no liability for any external decisions or actions taken on the basis of this document. Persons external to the Department of Environment and Science should satisfy themselves independently and by consulting their own professional advisors before embarking on any proposed course of action. If you need to access this document in a language other than English, please call the Translating and Interpreting Service (TIS National) on 131 450 and ask them to telephone Library Services on +61 7 3170 5470. This publication can be made available in an alternative format (e.g. -
Wet Tropics Lizards No
Tropical Topics A n i n t e r p r e t i v e n e w s l e t t e r f o r t h e t o u r i s m i n d u s t r y Wet tropics lizards No. 33 January 1996 Lizards tell a tale of history Notes from the A prickly forest skink from Cardwell and a prickly forest skink from Cooktown look the same but recent studies of their genetic make-up have Editor revealed hidden differences which tell a tale of history. While mammals and snakes are a The wet tropics contain the remnants Studies of birds, skinks, frogs, geckos fairly rare sight in the rainforests, of tropical rainforests which once and snails as well as some mammals lizards are one of the few types of covered much of Australia. As the revealed genetic breaks at exactly the animal we can be almost certain to climate became drier only the same location. It is thought that a dry see. mountainous regions of the north-east corridor cut through the wet tropics at coast remained constantly moist and this point for hundreds of thousands The wet tropics rainforests have an became the last refuges of Australia’s of years, preventing rainforest animals extraordinarily high number of lizard ancient tropical rainforests. on either side from mixing with each species — at least 14 — which are other at all. This affected not just found nowhere else. Some only However, the area currently occupied individual species but whole occur in very restricted areas such by rainforest has fluctuated. -
59550-Listing-Advice.Pdf
Advice to the Minister for the Environment, Heritage and the Arts from the Threatened Species Scientific Committee (the Committee) on Amendments to the list of Threatened Species under the Environment Protection and Biodiversity Conservation Act 1999 (EPBC Act) 1. Scientific name (common name) Nangura spinosa (Nangur Spiny Skink) 2. Description The Nangur Spiny Skink is a spiny-scaled skink that grows to a total length of approximately 19 cm (snout-vent length of 9.5 cm) (Covacevitch, Couper & James 1993; Wilson 2005). The Nangur Spiny Skink has been recorded in hoop pine plantation and in semi-evergreen vine thicket between 315-600 m altitude where it lives in single-entrance burrows. Burrows are usually occupied by a single adult or sub-adult skink, but may be shared by up to five individuals that can include up to three young and/or another adult or sub-adult skink. (Borsboom et al 2005). Burrow entrances average about 8 cm wide by 3 cm high (Borsboom et al 2005), and can have a smooth ‘resting platform’ in front approximately 11 cm wide by 8.5 cm long (Hannah et al 1997). Burrows have been recorded to be up to 60 cm in length (Covacevitch, Couper & James 1993; Wilson 2005). The Nangur Spiny Skink is suspected to be relatively sedentary, based on observations of burrow use, with some burrows in use for over eight years. The Nangur Spiny Skink can be active diurnally in front of its burrow entrance during Spring, Summer and Autumn (Covacevitch, Couper & James 1993; Hannah et al 1997; Borsboom et al 2005). -
First Record of the Alpine Water Skink, Eulamprus Kosciuskoi (Kinghorn
VOLUME 52 PART 2 ME M OIRS OF THE QUEENSLAND MUSEU M BRIS B ANE 30 APRIL 2008 © Queensland Museum PO Box 3300, South Brisbane 4101, Australia Phone 06 7 3840 7555 Fax 06 7 3846 1226 Email [email protected] Website www.qm.qld.gov.au National Library of Australia card number ISSN 0079-8835 NOTE Papers published in this volume and in all previous volumes of the Memoirs of the Queensland Museum may be reproduced for scientific research, individual study or other educational purposes. Properly acknowledged quotations may be made but queries regarding the republication of any papers should be addressed to the Editor in Chief. Copies of the journal can be purchased from the Queensland Museum Shop. A Guide to Authors is displayed at the Queensland Museum web site www.qm.qld.gov.au/organisation/publications/memoirs/guidetoauthors.pdf A Queensland Government Project Typeset at the Queensland Museum 238 MEMOIRS OF THE QUEENSLAND MUSEUM FIRST RECORD OF THE ALPINE WATER SKINK, in this position); a random scattering of dark spots and flecks EULAMPRUS KOSCIUSKOI (KINGHORN, 1932) along the lateral side of the tail (vs dark spots aligned in (SQUAMATA: SCINCIDAE) FROM QUEENSLAND. multiple transverse rows), and the body venter (in preserved Memoirs of the Queensland Museum 52(2): 238. 2008:–Water individuals) with a yellow tinge at least posteriorly (vs body Skinks (Eulamprus quoyii species group) are a lineage venter completely clouded blue-grey). (O’Connor & Moritz, 2003) of moderate-sized, diurnal skinks occurring in south-eastern and eastern Australia. They The locality for these specimens is 100km NNW of the are commonly located in proximity to moist environments nearest previous record of E.