Northern Goldfields Interconnect Pipeline Fauna Assessment (Kingfisher, 2020)
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Lake Pinaroo Ramsar Site
Ecological character description: Lake Pinaroo Ramsar site Ecological character description: Lake Pinaroo Ramsar site Disclaimer The Department of Environment and Climate Change NSW (DECC) has compiled the Ecological character description: Lake Pinaroo Ramsar site in good faith, exercising all due care and attention. DECC does not accept responsibility for any inaccurate or incomplete information supplied by third parties. No representation is made about the accuracy, completeness or suitability of the information in this publication for any particular purpose. Readers should seek appropriate advice about the suitability of the information to their needs. © State of New South Wales and Department of Environment and Climate Change DECC is pleased to allow the reproduction of material from this publication on the condition that the source, publisher and authorship are appropriately acknowledged. Published by: Department of Environment and Climate Change NSW 59–61 Goulburn Street, Sydney PO Box A290, Sydney South 1232 Phone: 131555 (NSW only – publications and information requests) (02) 9995 5000 (switchboard) Fax: (02) 9995 5999 TTY: (02) 9211 4723 Email: [email protected] Website: www.environment.nsw.gov.au DECC 2008/275 ISBN 978 1 74122 839 7 June 2008 Printed on environmentally sustainable paper Cover photos Inset upper: Lake Pinaroo in flood, 1976 (DECC) Aerial: Lake Pinaroo in flood, March 1976 (DECC) Inset lower left: Blue-billed duck (R. Kingsford) Inset lower middle: Red-necked avocet (C. Herbert) Inset lower right: Red-capped plover (C. Herbert) Summary An ecological character description has been defined as ‘the combination of the ecosystem components, processes, benefits and services that characterise a wetland at a given point in time’. -
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, -
Origin and Age of Australian Chenopodiaceae
ARTICLE IN PRESS Organisms, Diversity & Evolution 5 (2005) 59–80 www.elsevier.de/ode Origin and age of Australian Chenopodiaceae Gudrun Kadereita,Ã, DietrichGotzek b, Surrey Jacobsc, Helmut Freitagd aInstitut fu¨r Spezielle Botanik und Botanischer Garten, Johannes Gutenberg-Universita¨t Mainz, D-55099 Mainz, Germany bDepartment of Genetics, University of Georgia, Athens, GA 30602, USA cRoyal Botanic Gardens, Sydney, Australia dArbeitsgruppe Systematik und Morphologie der Pflanzen, Universita¨t Kassel, D-34109 Kassel, Germany Received 20 May 2004; accepted 31 July 2004 Abstract We studied the age, origins, and possible routes of colonization of the Australian Chenopodiaceae. Using a previously published rbcL phylogeny of the Amaranthaceae–Chenopodiaceae alliance (Kadereit et al. 2003) and new ITS phylogenies of the Camphorosmeae and Salicornieae, we conclude that Australia has been reached in at least nine independent colonization events: four in the Chenopodioideae, two in the Salicornieae, and one each in the Camphorosmeae, Suaedeae, and Salsoleae. Where feasible, we used molecular clock estimates to date the ages of the respective lineages. The two oldest lineages both belong to the Chenopodioideae (Scleroblitum and Chenopodium sect. Orthosporum/Dysphania) and date to 42.2–26.0 and 16.1–9.9 Mya, respectively. Most lineages (Australian Camphorosmeae, the Halosarcia lineage in the Salicornieae, Sarcocornia, Chenopodium subg. Chenopodium/Rhagodia, and Atriplex) arrived in Australia during the late Miocene to Pliocene when aridification and increasing salinity changed the landscape of many parts of the continent. The Australian Camphorosmeae and Salicornieae diversified rapidly after their arrival. The molecular-clock results clearly reject the hypothesis of an autochthonous stock of Chenopodiaceae dating back to Gondwanan times. -
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. -
Index of Handbook of the Mammals of the World. Vol. 9. Bats
Index of Handbook of the Mammals of the World. Vol. 9. Bats A agnella, Kerivoula 901 Anchieta’s Bat 814 aquilus, Glischropus 763 Aba Leaf-nosed Bat 247 aladdin, Pipistrellus pipistrellus 771 Anchieta’s Broad-faced Fruit Bat 94 aquilus, Platyrrhinus 567 Aba Roundleaf Bat 247 alascensis, Myotis lucifugus 927 Anchieta’s Pipistrelle 814 Arabian Barbastelle 861 abae, Hipposideros 247 alaschanicus, Hypsugo 810 anchietae, Plerotes 94 Arabian Horseshoe Bat 296 abae, Rhinolophus fumigatus 290 Alashanian Pipistrelle 810 ancricola, Myotis 957 Arabian Mouse-tailed Bat 164, 170, 176 abbotti, Myotis hasseltii 970 alba, Ectophylla 466, 480, 569 Andaman Horseshoe Bat 314 Arabian Pipistrelle 810 abditum, Megaderma spasma 191 albatus, Myopterus daubentonii 663 Andaman Intermediate Horseshoe Arabian Trident Bat 229 Abo Bat 725, 832 Alberico’s Broad-nosed Bat 565 Bat 321 Arabian Trident Leaf-nosed Bat 229 Abo Butterfly Bat 725, 832 albericoi, Platyrrhinus 565 andamanensis, Rhinolophus 321 arabica, Asellia 229 abramus, Pipistrellus 777 albescens, Myotis 940 Andean Fruit Bat 547 arabicus, Hypsugo 810 abrasus, Cynomops 604, 640 albicollis, Megaerops 64 Andersen’s Bare-backed Fruit Bat 109 arabicus, Rousettus aegyptiacus 87 Abruzzi’s Wrinkle-lipped Bat 645 albipinnis, Taphozous longimanus 353 Andersen’s Flying Fox 158 arabium, Rhinopoma cystops 176 Abyssinian Horseshoe Bat 290 albiventer, Nyctimene 36, 118 Andersen’s Fruit-eating Bat 578 Arafura Large-footed Bat 969 Acerodon albiventris, Noctilio 405, 411 Andersen’s Leaf-nosed Bat 254 Arata Yellow-shouldered Bat 543 Sulawesi 134 albofuscus, Scotoecus 762 Andersen’s Little Fruit-eating Bat 578 Arata-Thomas Yellow-shouldered Talaud 134 alboguttata, Glauconycteris 833 Andersen’s Naked-backed Fruit Bat 109 Bat 543 Acerodon 134 albus, Diclidurus 339, 367 Andersen’s Roundleaf Bat 254 aratathomasi, Sturnira 543 Acerodon mackloti (see A. -
Clearing Permit Decision Report
Clearing Permit Decision Report 1. Application details 1.1. Permit application details Permit application No.: 6807/1 Permit type: Purpose Permit 1.2. Proponent details Proponent’s name: Minjar Gold Pty Ltd 1.3. Property details Property: Mining Lease 59/406 Local Government Area: Shire of Yalgoo Colloquial name: Minjar Gold Project – TSF expansion 1.4. Application Clearing Area (ha) No. Trees Method of Clearing For the purpose of: 43.4 Mechanical Removal Mineral Production and associated activities 1.5. Decision on application Decision on Permit Application: Grant Decision Date: 3 December 2015 2. Site Information 2.1. Existing environment and information 2.1.1. Description of the native vegetation under application Vegetation Description The clearing permit application area has been broadly mapped as the following Beard vegetation associations: 202: Shrublands; mulga & Acacia quadrimarginea scrub; and 420: Shrublands; bowgada & jam scrub (GIS Database). A flora and fauna survey was conducted by Terratree Pty Ltd during July 2015 over an area of approximately 172.5 hectares, which includes the current clearing permit application area (Terratree, 2015). The following five vegetation communities were recorded within the survey area (Terratree, 2015): 1. AaAiTOS: Acacia aulacophylla, Acacia incurvaneura Tall Open Shrubland over Thryptomene costata, Micromyrtus trudgenii, Philotheca sericea Mid Open Shrubland; 2. AaS: Aluta aspera ssp. hesperia Shrubland over Borya sphaerocephala Herbland; 3. CcLOW: Callitris columellaris Low Open Woodland over Acacia ramulosa ssp. ramulosa, Acacia caesaneura Tall Sparse Shrubland over Eremophila georgei, Acacia tetragonophylla, Microcorys sp. Mt Gibson Mid Open Shrubland over mixed species Low Open Shrubland; 4. ArAsMlTCS: Acacia ramulosa ssp. ramulosa, Acacia sabina, Melaleuca leiocarpa Tall Closed Shrubland over Eremophila georgeii, Philotheca desertii ssp. -
Fitz-Stirling 2007-2017 Ten-Year Evaluation Review
Fitz-Stirling 2007-2017 Ten-year Evaluation Review Feb / 2018 P a g e | 1 Acknowledgements: This report has benefited greatly from the discussion and guidance on content, presentation and editing by Annette Stewart, Clair Dougherty and Simon Smale. Their expert assistance is greatly appreciated. Volunteers have played a major and vital role in the monitoring and survey program over the past 5 years and I thank all of those involved. Special thanks go to Dr Sandra Gilfillan for her continuing dedication to the wallaby monitoring and research program. Volunteers Aaron Gove, who provided the bird data analysis and Richard Thomas, who provided the bat data analysis, have made a large contribution to this report and I thank them. I sincerely thank Bill and Jane Thompson who have regularly carried out all the pool monitoring for several years. Thanks also to Barry Heydenrych, Greening Australia, who provided restoration data. Funding to assist the monitoring program and UAV surveys during 2015 was gratefully received from South Coast NRM as part of the Australian Government funded ‘Restoring Gondwana’ program. Funding vital for wallaby monitoring and research was provided by the Diversicon Foundation. Citation: Sanders, A. (2018). Fitz-Stirling 2007-2017 ten-year evaluation review. Unpublished report for Bush Heritage Australia. P a g e | 2 Contents Overview of Fitz-Stirling Project ........................................................................................................ 6 This report evaluates our conservation impact ................................................................................. -
Appendix a Fauna Survey Effort and Results
APPENDIX A FAUNA SURVEY EFFORT AND RESULTS October 2016 Prepared by Anderson Environment and Planning The Fauna Survey Effort (FSE) for the Biobanking Assessment Report has been guided by the following: The predict threatened species from within the Biobanking Credit Calculator; The Threatened Species Survey and Assessment Guidelines for developments and activities (working draft), NSW Department of Environment and Conservation (2004); The NSW Threatened Species Profile Database; and Previous fauna survey results from the site. The following Ecosystem Credit species have been recorded on the site during past or current survey work: Eastern Bentwing-bat (Miniopterus schreibersii oceanensis); Eastern False Pipistrelle (Falsistrellus tasmaniensis); Eastern Freetail-bat (Mormopterus norfolkensis); Greater Broad-nosed Bat (Scoteanax rueppellii); Grey-headed Flying-fox (Pteropus poliocephalus); Little Bentwing-bat (Miniopterus australis); Little Lorikeet (Glossopsitta pusilla); Long-nosed Potoroo (Potorous tridactylus); Powerful Owl (Ninox strenua); Squirrel Glider (Petaurus norfolcensis); Varied Sittella (Daphoenositta chrysoptera); Yellow-bellied Glider (Petaurus australis); Yellow-bellied Sheathtail-bat (Saccolaimus flaviventris). The following Species Credit species have been recorded on the site or surrounds during past survey work: Koala (Phascolarctos cinereus); Wallum Froglet (Crinia tinnula). Prepared by Anderson Environment and Planning Contents 1.0 Introduction .............................................................................................................................................. -
WOOD ANATOMY of CHENOPODIACEAE (AMARANTHACEAE S
IAWA Journal, Vol. 33 (2), 2012: 205–232 WOOD ANATOMY OF CHENOPODIACEAE (AMARANTHACEAE s. l.) Heike Heklau1, Peter Gasson2, Fritz Schweingruber3 and Pieter Baas4 SUMMARY The wood anatomy of the Chenopodiaceae is distinctive and fairly uni- form. The secondary xylem is characterised by relatively narrow vessels (<100 µm) with mostly minute pits (<4 µm), and extremely narrow ves- sels (<10 µm intergrading with vascular tracheids in addition to “normal” vessels), short vessel elements (<270 µm), successive cambia, included phloem, thick-walled or very thick-walled fibres, which are short (<470 µm), and abundant calcium oxalate crystals. Rays are mainly observed in the tribes Atripliceae, Beteae, Camphorosmeae, Chenopodieae, Hab- litzieae and Salsoleae, while many Chenopodiaceae are rayless. The Chenopodiaceae differ from the more tropical and subtropical Amaran- thaceae s.str. especially in their shorter libriform fibres and narrower vessels. Contrary to the accepted view that the subfamily Polycnemoideae lacks anomalous thickening, we found irregular successive cambia and included phloem. They are limited to long-lived roots and stem borne roots of perennials (Nitrophila mohavensis) and to a hemicryptophyte (Polycnemum fontanesii). The Chenopodiaceae often grow in extreme habitats, and this is reflected by their wood anatomy. Among the annual species, halophytes have narrower vessels than xeric species of steppes and prairies, and than species of nitrophile ruderal sites. Key words: Chenopodiaceae, Amaranthaceae s.l., included phloem, suc- cessive cambia, anomalous secondary thickening, vessel diameter, vessel element length, ecological adaptations, xerophytes, halophytes. INTRODUCTION The Chenopodiaceae in the order Caryophyllales include annual or perennial herbs, sub- shrubs, shrubs, small trees (Haloxylon ammodendron, Suaeda monoica) and climbers (Hablitzia, Holmbergia). -
Technical Report
A STRATEGIC FRAMEWORK FOR BIODIVERSITY CONSERVATION Report B: For practitioners of conservation planning Copyright text 2012 Southwest Australia Ecoregion Initiative. All rights reserved. Author: Danielle Witham, WWF-Australia First published: 2012 by the Southwest Australia Ecoregion Initiative. Any reproduction in full or in part of this publication must mention the title and credit the above-mentioned publisher as the copyright Cover Image: ©Richard McLellan Design: Three Blocks Left Design Printed by: SOS Print & Media Printed on Impact, a 100% post-consumer waste recycled paper. For copies of this document, please contact SWAEI Secretariat, PO Box 4010, Wembley, Western Australia 6913. This document is also available from the SWAEI website at http://www.swaecoregion.org SETTING THE CONTEXT i CONTENTS EXECUTIVE SUMMARY 1 ACKNOWLEDGEMENTS 2 SETTING THE CONTEXT 3 The Southwest Australia Ecoregion Initiative SUMMARY OF THE PROJECT METHODOLOGY 5 STEP 1. IDENTIFYING RELEVANT STAKEHOLDERS AND CLARIFYING ROLES 7 Expert engagement STEP 2. DEFINING PROJECT BOUNDARY 9 The boundary of the Southwest Australia Ecoregion STEP 3. APPLYING PLANNING UNITS TO PROJECT AREA 11 STEP 4. PREPARING AND CHOOSING SOFTWARE 13 Data identification 13 Conservation planning software 14 STEP 5. IDENTIFYING CONSERVATION FEATURES 16 Choosing conservation features 16 Fauna conservation features 17 Flora conservation features 21 Inland water body conservation features 22 Inland water species conservation features 27 Other conservation features 27 Threatened and Priority Ecological communities (TECs and PECs) 31 Vegetation conservation features 32 Vegetation connectivity 36 STEP 6. APPLYING CONSERVATION FEATURES TO PLANNING UNITS 38 STEP 7. SETTING TARGETS 40 Target formulae 40 Special formulae 42 STEP 8. IDENTIFYING AND DEFINING LOCK-INS 45 STEP 9. -
The Riparian Flora and Plant Communities of the Pilbara Region Of
DOI: 10.18195/issn.0313-122x.78(2).2015.485-513 Records of the Western Australian Museum, Supplement 78: 485–513 (2015). The riparian fl ora and plant communities of the Pilbara region of Western Australia M.N. Lyons Department of Parks and Wildlife, Science and Conservation Division, Kieran McNamara Conservation Science Centre, Locked Bag 104, Bentley Delivery Centre, Western Australia 6983, Australia. Email: [email protected] Abstract – A survey of riparian fl ora and plant communities was undertaken at 98 wetlands and rivers in the Pilbara region of Western Australia. Sampling was quadrat-based, with fl oristics, surface soils and wetland attributes recorded. Selected sites captured the full range of Pilbara wetland types including springs, river pools, claypans, salt marshes and rock pools. A total of 455 taxa was recorded from the survey sites, representing ca. 25% of the known fl ora of the Pilbara bioregion. The fl ora is dominated by taxa with Eremaean and tropical affi nities, with only six taxa endemic in the region. Of recorded taxa known from four or fewer bioregions, most are shared with the adjacent Carnarvon and Gascoyne bioregions rather than the adjoining internally draining deserts. Sixteen taxa of conservation signifi cance were documented, with claypans, the Fortescue Marsh, and Millstream and Karijini National Park sites dominating occurrences of rare species. Eight major groups were defi ned by classifying wetlands in terms of species presence/absence data. Floristic patterning was strongly aligned with the major wetland types (geomorphic/hydrological) used in the primary sampling stratifi cation. A combination of wetland morphology/hydrological setting, site edaphic attributes and distance to the coast were dominant variables related to riparian fl oristic composition. -
Conservation Advice and Included This Species in the Endangered Category, Effective from 04/07/2019 Conservation Advice Acacia Woodmaniorum
THREATENED SPECIES SCIENTIFIC COMMITTEE Established under the Environment Protection and Biodiversity Conservation Act 1999 The Minister approved this conservation advice and included this species in the Endangered category, effective from 04/07/2019 Conservation Advice Acacia woodmaniorum Woodman’s Wattle Summary of assessment Conservation status Acacia woodmaniorum has been found to be eligible for listing in the Endangered category, as outlined in the attached assessment. Reason for conservation assessment by the Threatened Species Scientific Committee This advice follows assessment of information provided by Western Australia as part of the Common Assessment Method process, to systematically review species that are inconsistently listed under the EPBC Act and relevant Western Australian legislation or lists. More information on the Common Assessment Method is available at: http://www.environment.gov.au/biodiversity/threatened/cam The information in this assessment has been compiled by the relevant state/territory government. In adopting this assessment under the EPBC Act, this document forms the Approved Conservation Advice for this species as required under s266B of the EPBC Act. Public consultation Notice of the proposed amendment and a consultation document was made available for public comment for at least 30 business days between 14 August 2018 and 25 September 2018. Any comments received that were relevant to the survival of the species were considered by the Committee as part of the assessment process. Recovery plan A recovery plan for this species under the EPBC Act is not recommended, because the Approved Conservation Advice provides sufficient direction to implement priority actions and mitigate against key threats. The relevant state/territory may decide to develop a plan under its equivalent legislation.