Action Statement Floraflora and and Fauna Fauna Guarantee Guarantee Act Act 1988 1988 No
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Guidelines for Keeping Venomous Snakes in the NT
GUIDELINES FOR KEEPING VENOMOUS SNAKES IN THE NT Venomous snakes are potentially dangerous to humans, and for this reason extreme caution must be exercised when keeping or handling them in captivity. Prospective venomous snake owners should be well informed about the needs and requirements for keeping these animals in captivity. Permits The keeping of protected wildlife in the Northern Territory is regulated by a permit system under the Territory Parks and Wildlife Conservation Act 2006 (TPWC Act). Conditions are included on permits, and the Parks and Wildlife Commission of the Northern Territory (“PWCNT”) may issue infringement notices or cancel permits if conditions are breached. A Permit to Keep Protected Wildlife enables people to legally possess native vertebrate animals in captivity in the Northern Territory. The permit system assists the PWCNT to monitor wildlife kept in captivity and to detect any illegal activities associated with the keeping of, and trade in, native wildlife. Venomous snakes are protected throughout the Northern Territory and may not be removed from the wild without the appropriate licences and permits. People are required to hold a Keep Permit (Category 1–3) to legally keep venomous snakes in the Northern Territory. Premises will be inspected by PWCNT staff to evaluate their suitability prior to any Keep Permit (Category 1– 3) being granted. Approvals may also be required from local councils, the Northern Territory Planning Authority, and the Department of Health and Community Services. Consignment of venomous snakes between the Northern Territory and other States and Territories can only be undertaken with an appropriate import / export permit. There are three categories of venomous snake permitted to be kept in captivity in the Northern Territory: Keep Permit (Category 1) – Mildly Dangerous Venomous Keep Permit (Category 2) – Dangerous Venomous Keep Permit (Category 3) – Highly Dangerous Venomous Venomous snakes must be obtained from a legal source (i.e. -
Evaluating the Effectiveness of Salvage and Translocation of Striped Legless Lizards
Evaluating the effectiveness of salvage and translocation of Striped Legless Lizards Megan O’Shea February 2013 Arthur Rylah Institute for Environmental Research Technical Report Series No. 243 Evaluating the effectiveness of salvage and translocation of Striped Legless Lizards Megan O’Shea February 2013 Arthur Rylah Institute for Environmental Research Department of Sustainability and Environment Heidelberg, Victoria Report produced by: Arthur Rylah Institute for Environmental Research Department of Sustainability and Environment PO Box 137 Heidelberg, Victoria 3084 Phone (03) 9450 8600 Website: www.dse.vic.gov.au/ari © State of Victoria, Department of Sustainability and Environment 2013 This publication is copyright. Apart from fair dealing for the purposes of private study, research, criticism or review as permitted under the Copyright Act 1968 , no part may be reproduced, copied, transmitted in any form or by any means (electronic, mechanical or graphic) without the prior written permission of the State of Victoria, Department of Sustainability and Environment. All requests and enquiries should be directed to the Customer Service Centre, 136 186 or email [email protected] Citation: O’Shea, M. (2013). Evaluating the effectiveness of salvage and translocation of Striped Legless Lizards. Arthur Rylah Institute for Environmental Research Technical Report Series No. 243. Department of Sustainability and Environment, Heidelberg. ISSN 1835-3827 (print) ISSN 1835-3835 (online) ISBN 978-1-74287-763-1 (print) ISBN 978-1-74287-764-8 (online) Disclaimer: This publication may be of assistance to you but the State of Victoria and its employees do not guarantee that the publication is without flaw of any kind or is wholly appropriate for your particular purposes and therefore disclaims all liability for any error, loss or other consequence which may arise from you relying on any information in this publication. -
33234.VBB.EPBC.PD.Draft.04092020
Victorian Big Battery Storage Facility, 680 Ballan Road Moorabool, Victoria: Preliminary Documentation for EPBC 2020/8614 Prepared for Neoen Australia Pty Ltd 04 September 2020 Biosis offices Document information NEW SOUTH WALES Report to: Neoen Australia Pty Ltd Albury Prepared by: Daniel Gilmore and Stephen Mueck Phone: (02) 6069 9200 Email: [email protected] Biosis project No.: 33234 File name: 33234.VBB.EPBC.PD.Draft.21052020 Newcastle Phone: (02) 4911 4040 Citation: Biosis 2020. Victorian Big Battery Storage Facility, 680 Ballan Road Email: [email protected] Moorabool, Victoria: Preliminary Documentation for EPBC 2020/8614. Report for Neoen Australia. Author: Gilmore, D., & Mueck, S. Biosis Pty Ltd, Sydney Melbourne. Project no. 33234 Phone: (02) 9101 8700 Email: [email protected] Western Sydney Document control Phone: (02) 9101 8700 Email: [email protected] Version Internal reviewer Date issued Wollongong Draft version 01 IS 17/06/2020 Phone: (02) 4201 1090 Email: [email protected] Final version 01 Determined with XX/09/2020 input from DAWE Acknowledgements VICTORIA Ballarat Phone: (03) 5304 4250 Biosis acknowledges the contribution of the following people and Email: [email protected] organisations in in the production of this report: Melbourne (Head Office) • Neoen Australia: Matthew Parton Phone: (03) 8686 4800 Email: [email protected] • GHD (Melbourne): Brad George Wangaratta Biosis staff involved in this project were: Phone: (03) 5718 6900 Email: [email protected] • Sonika Kumar (mapping). Biosis Pty Ltd This document is and shall remain the property of Biosis Pty Ltd. The document may only be used for the purposes for which it was commissioned and in accordance with the Terms of the Engagement for the commission. -
Ecology and Behaviour of Burton's Legless Lizard (Lialis Burtonis, Pygopodidae) in Tropical Australia
Asian Herpetological Research 2013, 4(1): 9–21 DOI: 10.3724/SP.J.1245.2013.00009 Ecology and Behaviour of Burton’s Legless Lizard (Lialis burtonis, Pygopodidae) in Tropical Australia Michael WALL1, 2 and Richard SHINE1* 1 School of Biological Sciences A08, University of Sydney, NSW 2006, Australia 2 Current address: 4940 Anza St. No. 4, San Francisco, CA 94121, USA Abstract The elongate, functionally limbless flap-footed lizards (family Pygopodidae) are found throughout Australia, ranging into southern New Guinea. Despite their diversity and abundance in most Australian ecosystems, pygopodids have attracted little scientific study. An intensive ecological study of one pygopodid, Burton’s legless lizard (Lialis burtonis Gray 1835), was conducted in Australia’s tropical Northern Territory. L. burtonis eats nothing but other lizards, primarily skinks, and appears to feed relatively infrequently (only 20.8% of stomachs contained prey). Ovulation and mating occur chiefly in the late dry-season (beginning around September), and most egg-laying takes place in the early to middle wet-season (November–January). Females can lay multiple clutches per year, some of which may be fertilised with stored sperm. Free-ranging L. burtonis are sedentary ambush foragers, with radio-tracked lizards moving on average < 5 m/day. Most foraging is done diurnally, but lizards may be active at any time of day or night. Radiotracked lizards were usually found in leaf-litter microhabitats, a preference that was also evident in habitat-choice experiments using field enclosures. Lizards typically buried themselves in 6–8 cm of litter; at this depth, they detect potential prey items while staying hidden from predators and prey and avoiding lethally high temperatures. -
Controlled Animals
Environment and Sustainable Resource Development Fish and Wildlife Policy Division Controlled Animals Wildlife Regulation, Schedule 5, Part 1-4: Controlled Animals Subject to the Wildlife Act, a person must not be in possession of a wildlife or controlled animal unless authorized by a permit to do so, the animal was lawfully acquired, was lawfully exported from a jurisdiction outside of Alberta and was lawfully imported into Alberta. NOTES: 1 Animals listed in this Schedule, as a general rule, are described in the left hand column by reference to common or descriptive names and in the right hand column by reference to scientific names. But, in the event of any conflict as to the kind of animals that are listed, a scientific name in the right hand column prevails over the corresponding common or descriptive name in the left hand column. 2 Also included in this Schedule is any animal that is the hybrid offspring resulting from the crossing, whether before or after the commencement of this Schedule, of 2 animals at least one of which is or was an animal of a kind that is a controlled animal by virtue of this Schedule. 3 This Schedule excludes all wildlife animals, and therefore if a wildlife animal would, but for this Note, be included in this Schedule, it is hereby excluded from being a controlled animal. Part 1 Mammals (Class Mammalia) 1. AMERICAN OPOSSUMS (Family Didelphidae) Virginia Opossum Didelphis virginiana 2. SHREWS (Family Soricidae) Long-tailed Shrews Genus Sorex Arboreal Brown-toothed Shrew Episoriculus macrurus North American Least Shrew Cryptotis parva Old World Water Shrews Genus Neomys Ussuri White-toothed Shrew Crocidura lasiura Greater White-toothed Shrew Crocidura russula Siberian Shrew Crocidura sibirica Piebald Shrew Diplomesodon pulchellum 3. -
Draft Animal Keepers Species List
Revised NSW Native Animal Keepers’ Species List Draft © 2017 State of NSW and Office of Environment and Heritage With the exception of photographs, the State of NSW and Office of Environment and Heritage are pleased to allow this material to be reproduced in whole or in part for educational and non-commercial use, provided the meaning is unchanged and its source, publisher and authorship are acknowledged. Specific permission is required for the reproduction of photographs. The Office of Environment and Heritage (OEH) has compiled this report in good faith, exercising all due care and attention. No representation is made about the accuracy, completeness or suitability of the information in this publication for any particular purpose. OEH shall not be liable for any damage which may occur to any person or organisation taking action or not on the basis of this publication. Readers should seek appropriate advice when applying the information to their specific needs. All content in this publication is owned by OEH and is protected by Crown Copyright, unless credited otherwise. It is licensed under the Creative Commons Attribution 4.0 International (CC BY 4.0), subject to the exemptions contained in the licence. The legal code for the licence is available at Creative Commons. OEH asserts the right to be attributed as author of the original material in the following manner: © State of New South Wales and Office of Environment and Heritage 2017. Published by: Office of Environment and Heritage 59 Goulburn Street, Sydney NSW 2000 PO Box A290, -
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. -
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. -
Berriquin LWMP Wildlife
Berriquin Wildlife Murray Land & Water Management Plan Wildlife Survey 2005-2006 Matthew Herring David Webb Michael Pisasale INTRODUCTION Why do a wildlife survey? 106 farms and were surveyed One of the great things about between June 2005 and March living in rural Australia is all the 2006. They incorporated a range wildlife that we share the land- of vegetation types (e.g. Black scape with. Historically, humans Box Woodland) as well as reveg- have impacted on the survival of etation on previously cleared many native plants and animals. land and constructed wetlands. Fortunately, there is a grow- Methods used to survey wildlife ing commitment in the country included: to wildlife conservation on the farm. As we improve our knowl- - Bird surveys edge and understanding of the - Log rolling for reptiles and local landscape and the animals frogs and plants that live in it we will - Spotlighting for mammals, rep be in a much better position to tiles and nocturnal birds conserve and enhance our natu- - Elliot traps for small mammals ral heritage for future genera- and reptiles tions. - Pitfall trapping for reptiles and frogs This wildlife survey was an ini- - Harp traps for bats tiative of the Berriquin Land & - Using the “Anabat” to record Water Management Plan (LWMP) bat calls M.Herring Working Group and is the largest - Call broadcasting to attract Wildlife expert Adam Bester and most extensive ever un- birds with 11 Little Forest Bats, one dertaken in the area. Berriquin of Berriquin’s most abundant was one of four LWMP areas that Other targeted methods were mammals. -
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. -
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.