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Agonimia Opuntiella
Pertusaria scutellifera is a New Zealand endemic corticolous on several species of Dracophyllum and Nothofagus. Its asci are one-spored, and its spores can reach more than 180 µm in length. The photomicrograph on the cover looks like a differential interference image, but in fact was produced simply by sliding a piece of opaque paper partway across the condenser lens of the microscope to generate shadows. The technique has been whimsically called “ha’penny optics”. CONTENTS ADDITIONAL LICHEN RECORDS FROM AUSTRALIA Aptroot, A (73). Agonimia opuntiella................................................................................. 3 ARTICLES Ludwig, L—Marginal soralia and conidiomata in Icmadophila splachnirima (Icmado- philaceae) from southern New Zealand ......................................................................4 Øvstedal, DO; Fryday, AM—A new species of Protopannaria (Pannariaceae, Ascomy- cota) from the southern New Zealand shelf islands, and additional records of Pro- topannaria from South America .................................................................................. 12 Elix, JA—Three new species of Heterodermia (Physciaceae, Ascomycota) from Aus- tralia ............................................................................................................................... 16 Elix, JA—Lichen phytochemistry III: further additions and amendments ............ 22 Elix, JA; Archer, AW—Pertusaria cryptostoma Müll.Arg., the earliest name for Pertus- aria limbata Vain. .......................................................................................................... -
Amphibian Abundance and Detection Trends During a Large Flood in a Semi-Arid Floodplain Wetland
Herpetological Conservation and Biology 11:408–425. Submitted: 26 January 2016; Accepted: 2 September 2016; Published: 16 December 2016. Amphibian Abundance and Detection Trends During a Large Flood in a Semi-Arid Floodplain Wetland Joanne F. Ocock1,4, Richard T. Kingsford1, Trent D. Penman2, and Jodi J.L. Rowley1,3 1Centre for Ecosystem Science, School of Biological, Earth and Environmental Sciences, UNSW Australia, Sydney, New South Wales, 2052, Australia 2Centre for Environmental Risk Management of Bushfires, Institute of Conservation Biology and Environmental Management, University of Wollongong, Wollongong, New South Wales 2522, Australia 3Australian Museum Research Institute, Australian Museum, 6 College St, Sydney, New South Wales 2010, Australia 4Corresponding author, email: [email protected] Abstract.—Amphibian abundance and occupancy are often reduced in regulated river systems near dams, but com- paratively little is known about how they are affected on floodplain wetlands downstream or the effects of actively managed flows. We assessed frog diversity in the Macquarie Marshes, a semi-arid floodplain wetland of conserva- tion significance, identifying environmental variables that might explain abundances and detection of species. We collected relative abundance data of 15 amphibian species at 30 sites over four months, coinciding with a large natural flood. We observed an average of 39.9 ± (SE) 4.3 (range, 0-246) individuals per site survey, over 47 survey nights. Three non-burrowing, ground-dwelling species were most abundant at temporarily flooded sites with low- growing aquatic vegetation (e.g., Limnodynastes tasmaniensis, Limnodynastes fletcheri, Crinia parinsignifera). Most arboreal species (e.g., Litoria caerulea) were more abundant in wooded habitat, regardless of water permanency. -
Threat Abatement Plan
gus resulting in ch fun ytridio trid myc chy osis ith w s n ia ib h p m a f o n o i t THREAT ABATEMENTc PLAN e f n I THREAT ABATEMENT PLAN INFECTION OF AMPHIBIANS WITH CHYTRID FUNGUS RESULTING IN CHYTRIDIOMYCOSIS Department of the Environment and Heritage © Commonwealth of Australia 2006 ISBN 0 642 55029 8 Published 2006 This work is copyright. Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from the Commonwealth, available from the Department of the Environment and Heritage. Requests and inquiries concerning reproduction and rights should be addressed to: Assistant Secretary Natural Resource Management Policy Branch Department of the Environment and Heritage PO Box 787 CANBERRA ACT 2601 This publication is available on the Internet at: www.deh.gov.au/biodiversity/threatened/publications/tap/chytrid/ For additional hard copies, please contact the Department of the Environment and Heritage, Community Information Unit on 1800 803 772. Front cover photo: Litoria genimaculata (Green-eyed tree frog) Sequential page photo: Taudactylus eungellensis (Eungella day frog) Banner photo on chapter pages: Close up of the skin of Litoria genimaculata (Green-eyed tree frog) ii Foreword ‘Infection of amphibians with chytrid fungus resulting Under the EPBC Act the Australian Government in chytridiomycosis’ was listed in July 2002 as a key implements the plan in Commonwealth areas and seeks threatening process under the Environment Protection the cooperation of the states and territories where the and Biodiversity Conservation Act 1999 (EPBC Act). disease impacts within their jurisdictions. -
Maritime Southeast Asia and Oceania Regional Focus
November 2011 Vol. 99 www.amphibians.orgFrogLogNews from the herpetological community Regional Focus Maritime Southeast Asia and Oceania INSIDE News from the ASG Regional Updates Global Focus Recent Publications General Announcements And More..... Spotted Treefrog Nyctixalus pictus. Photo: Leong Tzi Ming New The 2012 Sabin Members’ Award for Amphibian Conservation is now Bulletin open for nomination Board FrogLog Vol. 99 | November 2011 | 1 Follow the ASG on facebook www.facebook.com/amphibiansdotor2 | FrogLog Vol. 99| November 2011 g $PSKLELDQ$UN FDOHQGDUVDUHQRZDYDLODEOH 7KHWZHOYHVSHFWDFXODUZLQQLQJSKRWRVIURP $PSKLELDQ$UN¶VLQWHUQDWLRQDODPSKLELDQ SKRWRJUDSK\FRPSHWLWLRQKDYHEHHQLQFOXGHGLQ $PSKLELDQ$UN¶VEHDXWLIXOZDOOFDOHQGDU7KH FDOHQGDUVDUHQRZDYDLODEOHIRUVDOHDQGSURFHHGV DPSKLELDQDUN IURPVDOHVZLOOJRWRZDUGVVDYLQJWKUHDWHQHG :DOOFDOHQGDU DPSKLELDQVSHFLHV 3ULFLQJIRUFDOHQGDUVYDULHVGHSHQGLQJRQ WKHQXPEHURIFDOHQGDUVRUGHUHG±WKHPRUH \RXRUGHUWKHPRUH\RXVDYH2UGHUVRI FDOHQGDUVDUHSULFHGDW86HDFKRUGHUV RIEHWZHHQFDOHQGDUVGURSWKHSULFHWR 86HDFKDQGRUGHUVRIDUHSULFHGDW MXVW86HDFK 7KHVHSULFHVGRQRWLQFOXGH VKLSSLQJ $VZHOODVRUGHULQJFDOHQGDUVIRU\RXUVHOIIULHQGV DQGIDPLO\ZK\QRWSXUFKDVHVRPHFDOHQGDUV IRUUHVDOHWKURXJK\RXU UHWDLORXWOHWVRUIRUJLIWV IRUVWDIIVSRQVRUVRUIRU IXQGUDLVLQJHYHQWV" 2UGHU\RXUFDOHQGDUVIURPRXUZHEVLWH ZZZDPSKLELDQDUNRUJFDOHQGDURUGHUIRUP 5HPHPEHU±DVZHOODVKDYLQJDVSHFWDFXODUFDOHQGDU WRNHHSWUDFNRIDOO\RXULPSRUWDQWGDWHV\RX¶OODOVREH GLUHFWO\KHOSLQJWRVDYHDPSKLELDQVDVDOOSUR¿WVZLOOEH XVHGWRVXSSRUWDPSKLELDQFRQVHUYDWLRQSURMHFWV ZZZDPSKLELDQDUNRUJ FrogLog Vol. 99 | November -
Frogs of the Perth Region – Darling Range
FROGS OF THE PERTH REGION Darling Range Eight species of frogs are found commonly along streams and in the many small swamps in the Darling Range east of Perth. All of these species breed during the wetter months between late autumn and early spring. B. Maryan D. Robinson Whooping Frog Crawling Toadlet Heleioporus inornatus Pseudophryne guentheri BUILD: stout round body and short limbs, BUILD: flattened body, small head and short males have black nuptial spine on first finger limbs LENGTH: maximum length 7cm LENGTH: maximum length 3.5cm LOOK FOR: uniformly copper brown back, LOOK FOR: ‘warty’ back mottled with browns flanks may be mottled with white, grey or and grey, belly blotchy with black on white yellow background, crawls BREEDING SEASON: late autumn BREEDING SEASON: winter MALE CALL: ‘whoop whoop whoop’ MALE CALL: short, sharp grating sound B. Maryan D. Robinson Sand Frog Western Spotted Frog Heleioporus psammophilus Heleioporus albopunctatus BUILD: robust body with short limbs, males BUILD: large with a robust build may have black nuptial spine on first finger LENGTH: maximum length 8.5cm LENGTH: maximum length 6cm LOOK FOR: white or yellow spots on LOOK FOR: back brown to dark grey. Pale chocolate brown body coloured bumps on lower flanks BREEDING SEASON: late autumn BREEDING SEASON: late autumn MALE CALL: short, high pitched ‘coo’ MALE CALL: high pitched trilling ‘purr’ D. Robinson D. Robinson Humming Frog Hooting Frog Neobatrachus pelobatoides Heleioporus barycragus BUILD: medium size, flat broad head, robust BUILD: males have massive front arms and with short legs black nuptial spine on first finger LENGTH: maximum length 4.5cm LENGTH: maximum length 9cm LOOK FOR: back patterns with base colour LOOK FOR: greyish to chocolate brown body of green or grey with darker green or brown with scattering of yellow spots on its flanks irregular patterns. -
Spatial Ecology of the Giant Burrowing Frog (Heleioporus Australiacus): Implications for Conservation Prescriptions
University of Wollongong Research Online Faculty of Science - Papers (Archive) Faculty of Science, Medicine and Health January 2008 Spatial ecology of the giant burrowing frog (Heleioporus australiacus): implications for conservation prescriptions Trent D. Penman University of Wollongong, [email protected] F Lemckert M J Mahony Follow this and additional works at: https://ro.uow.edu.au/scipapers Part of the Life Sciences Commons, Physical Sciences and Mathematics Commons, and the Social and Behavioral Sciences Commons Recommended Citation Penman, Trent D.; Lemckert, F; and Mahony, M J: Spatial ecology of the giant burrowing frog (Heleioporus australiacus): implications for conservation prescriptions 2008, 179-186. https://ro.uow.edu.au/scipapers/724 Research Online is the open access institutional repository for the University of Wollongong. For further information contact the UOW Library: [email protected] Spatial ecology of the giant burrowing frog (Heleioporus australiacus): implications for conservation prescriptions Abstract Management of threatened anurans requires an understanding of a species’ behaviour and habitat requirements in both the breeding and non-breeding environments. The giant burrowing frog (Heleioporus australiacus) is a threatened species in south-eastern Australia. Little is known about its habitat requirements, creating difficulties in vde eloping management strategies for the species.Weradio-tracked 33 individual H. australiacus in order to determine their habitat use and behaviour. Data from 33 frogs followed for between 5 and 599 days show that individuals spend little time near (<15 >m) their breeding sites (mean 4.7 days for males and 6.3 days for females annually). Most time is spent in distinct non- breeding activity areas 20–250m from the breeding sites. -
Abandoned Australia’S Forest Wildlife in Crisis
Abandoned Australia’s forest wildlife in crisis Photo: Endangered Spotted-tailed Quoll by award-winning nature photographer David Gallan. Used with permission. March 2019 (Updated July 2019) Contents Part 1: A sample of threatened forest-dwelling fauna species at risk from logging 3 Comparison between ‘RFA forests’ and habitat for critically endangered species 5 Regent Honeyeater (NSW) 6 Western Ringtail Possum (WA) 7 Swift Parrot (NSW/Tas/Vic) 8 Leadbeater’s Possum (Vic) 9 Barred Galaxias (Vic) 10 Giant Freshwater Crayfish (Tas) 11 Koala (NSW/Vic) 12 Forest Red-tailed Black Cockatoo (WA) 13 Giant Barred Frog (NSW) 14 Numbat (WA) 15 Spotted-tailed Quoll (NSW/Vic) 16 Greater Glider (NSW/Vic) 17 Large Forest Owls: Masked Owl, Sooty Owl, Powerful Owl (NSW/Tas/Vic) 18 Further threatened forest-dwelling, logging-impacted species 20 Part 2: Summary of new laws and proposals for new protected areas 25 Part 3: Case studies: Threatened species under new RFAs and accredited logging plans 29 3.1 NSW ‘Integrated Forestry Operations Approvals’ (IFOAs) 30 3.2 Victoria: State of the Forests Report documents species decline 31 3.3 Tasmania 31 Part 4: Relevant court cases and rulings and their implications 32 4.1 Enforcement of EPBC Act in relation to threatened species 33 Appendix 1: The total number of EPBC-listed, forest-dwelling species in Australia 34 Appendix 2: Key threatening processes 35 Appendix 3: FSC HCV categories 37 Acknowledgements and selected references 38 The Wilderness Society acknowledges the First Nations peoples of the lands and seas on which we work across Australia, and recognises their continuing connection to land, water and community. -
Water Balance of Field-Excavated Aestivating Australian Desert Frogs
3309 The Journal of Experimental Biology 209, 3309-3321 Published by The Company of Biologists 2006 doi:10.1242/jeb.02393 Water balance of field-excavated aestivating Australian desert frogs, the cocoon- forming Neobatrachus aquilonius and the non-cocooning Notaden nichollsi (Amphibia: Myobatrachidae) Victoria A. Cartledge1,*, Philip C. Withers1, Kellie A. McMaster1, Graham G. Thompson2 and S. Don Bradshaw1 1Zoology, School of Animal Biology, MO92, University of Western Australia, Crawley, Western Australia 6009, Australia and 2Centre for Ecosystem Management, Edith Cowan University, 100 Joondalup Drive, Joondalup, Western Australia 6027, Australia *Author for correspondence (e-mail: [email protected]) Accepted 19 June 2006 Summary Burrowed aestivating frogs of the cocoon-forming approaching that of the plasma. By contrast, non-cocooned species Neobatrachus aquilonius and the non-cocooning N. aquilonius from the dune swale were fully hydrated, species Notaden nichollsi were excavated in the Gibson although soil moisture levels were not as high as calculated Desert of central Australia. Their hydration state (osmotic to be necessary to maintain water balance. Both pressure of the plasma and urine) was compared to the species had similar plasma arginine vasotocin (AVT) moisture content and water potential of the surrounding concentrations ranging from 9.4 to 164·pg·ml–1, except for soil. The non-cocooning N. nichollsi was consistently found one cocooned N. aquilonius with a higher concentration of in sand dunes. While this sand had favourable water 394·pg·ml–1. For both species, AVT showed no relationship potential properties for buried frogs, the considerable with plasma osmolality over the lower range of plasma spatial and temporal variation in sand moisture meant osmolalities but was appreciably increased at the highest that frogs were not always in positive water balance with osmolality recorded. -
National Recovery Plan for the Stuttering Frog Mixophyes Balbus
National Recovery Plan for the Stuttering Frog Mixophyes balbus David Hunter and Graeme Gillespie Prepared by David Hunter and Graeme Gillespie (Department of Sustainability and Environment, Victoria). Published by the Victorian Government Department of Sustainability and Environment (DSE) Melbourne, October 2011. © State of Victoria Department of Sustainability and Environment 2010 This publication is copyright. No part may be reproduced by any process except in accordance with the provisions of the Copyright Act 1968. Authorised by the Victorian Government, 8 Nicholson Street, East Melbourne. ISBN 978-1-74242-369-2 (online) This is a Recovery Plan prepared under the Commonwealth Environment Protection and Biodiversity Conservation Act 1999, with the assistance of funding provided by the Australian Government. This Recovery Plan has been developed with the involvement and cooperation of a range of stakeholders, but individual stakeholders have not necessarily committed to undertaking specific actions. The attainment of objectives and the provision of funds may be subject to budgetary and other constraints affecting the parties involved. Proposed actions may be subject to modification over the life of the plan due to changes in knowledge. 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 that may arise from you relying on any information in this publication. An electronic version of this document is available on the Department of the Environment, Water, Heritage and the Arts website www.environment.gov.au For more information contact the DSE Customer Service Centre 136 186 Citation: Hunter, D. -
2219573-REP-Marine Assessment Report AR
Appendix L – Marine Assessment GHD | Report for Hunter Water Corporation - Belmont Drought Response Desalination Plant, 2219573 Hunter Water Corporation Belmont Drought Response Desalination Plant Marine Environment Assessment Amendment Report July 2020 Table of contents 1. Introduction..................................................................................................................................... 1 1.1 Background .......................................................................................................................... 1 1.2 Purpose and structure of this report .................................................................................... 2 2. Project changes ............................................................................................................................. 4 2.1 Overview .............................................................................................................................. 4 2.2 Key features of the amended Project .................................................................................. 4 3. Methodology ................................................................................................................................... 7 3.1 Review of relevant legislation .............................................................................................. 7 3.2 Review of databases and searches ..................................................................................... 7 3.3 Review of previous marine ecology reports ........................................................................ -
Two Hundred and Ten Years Looking for the Giant Burrowing Frog
Two hundred and ten years looking for the Giant Burrowing Frog 1 2 Trent Penman , Francis Lemckert and Michael Mahony' 'School of Environmental and Life Sciences, University of Newcastle, N.S.W 2308,Australia 2Biodiversity Systems, Research and Development Division, Forests NSW P.O Box I 00 Beecroft, N.S.W 2119 Australia. Email for corresponding author: [email protected] The giant burrowing frog Heleioporusaustraliacus (Shaw) is a large, morphologically distinctive, but Downloaded fromhttp://meridian.allenpress.com/australian-zoologist/article-pdf/32/4/597/1471522/az_2004_005.pdf by gueston26September2021 cryptic frog found in south eastern Australia. This paper reviews the literature pertaining to the Giant Burrowing Frog. It is a forest dependent species found on the coast and adjacent ranges of south-eastern Australia, with five congeners in south-west Western Australia. The species is listed as vulnerable in NSW and Victoria and under Commonwealth legislation, although there is no obvious cause for a decline nor is it clear how much decline has occurred. Proposed threats to the species survival include forestry operations, habitat destruction, introduced species, pollutants, increased UV and disease.A large gap exists in the species distributional records and H. australiacusmay represent two distinct species, although the evidence for this remains inconclusive. Standard detection methods for frogs do not apply well to the Giant Burrowing Frog and alternative methods are required to provide a more detailed understanding of its ecology and distribution. Key words: review, conservation, Heleioporus, management, amphibian Introduction Despite being one of the first frogs described from The review brings together all known records from various Australia, there has been very little research into museum specimens, the published literature and previous the ecology of the Giant Burrowing Frog Heleioporus collations of habitat requirements. -
ARAZPA Amphibian Action Plan
Appendix 1 to Murray, K., Skerratt, L., Marantelli, G., Berger, L., Hunter, D., Mahony, M. and Hines, H. 2011. Guidelines for minimising disease risks associated with captive breeding, raising and restocking programs for Australian frogs. A report for the Australian Government Department of Sustainability, Environment, Water, Population and Communities. ARAZPA Amphibian Action Plan Compiled by: Graeme Gillespie, Director Wildlife Conservation and Science, Zoos Victoria; Russel Traher, Amphibian TAG Convenor, Curator Healesville Sanctuary Chris Banks, Wildlife Conservation and Science, Zoos Victoria. February 2007 1 1. Background Amphibian species across the world have declined at an alarming rate in recent decades. According to the IUCN at least 122 species have gone extinct since 1980 and nearly one third of the world’s near 6,000 amphibian species are classified as threatened with extinction, placing the entire class at the core of the current biodiversity crisis (IUCN, 2006). Australasia too has experienced significant declines; several Australian species are considered extinct and nearly 25% of the remainder are threatened with extinction, while all four species native to New Zealand are threatened. Conventional causes of biodiversity loss, habitat destruction and invasive species, are playing a major role in these declines. However, emergent disease and climate change are strongly implicated in many declines and extinctions. These factors are now acting globally, rapidly and, most disturbingly, in protected and near pristine areas. Whilst habitat conservation and mitigation of threats in situ are essential, for many taxa the requirement for some sort of ex situ intervention is mounting. In response to this crisis there have been a series of meetings organised by the IUCN (World Conservation Union), WAZA (World Association of Zoos & Aquariums) and CBSG (Conservation Breeding Specialist Group, of the IUCN Species Survival Commission) around the world to discuss how the zoo community can and should respond.