Threatened Species Conservation Act 1995 No 101
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Banksia Vincentia (Proteaceae), a New Species Known from Fourteen Plants from South-Eastern New South Wales, Australia
Phytotaxa 163 (5): 269–286 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ Article PHYTOTAXA Copyright © 2014 Magnolia Press ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.163.5.3 Could this be Australia’s rarest Banksia? Banksia vincentia (Proteaceae), a new species known from fourteen plants from south-eastern New South Wales, Australia MARGARET L. STIMPSON1, JEREMY J. BRUHL1 & PETER H. WESTON2 1 Botany, School of Environmental and Rural Science, University of New England, Armidale NSW 2351 Australia Corresponding Author Email: [email protected] 2 National Herbarium of New South Wales, Royal Botanic Garden Sydney, Mrs Macquaries Road, Sydney, NSW 2000, Australia Abstract Possession of hooked, distinctively discolorous styles, a broadly flabellate common bract subtending each flower pair, and a lignotuber place a putative new species, Banksia sp. Jervis Bay, in the B. spinulosa complex. Phenetic analysis of individuals from all named taxa in the B. spinulosa complex, including B. sp. Jervis Bay, based on leaf, floral, seed and bract characters support recognition of this species, which is described here as Banksia vincentia M.L.Stimpson & P.H.Weston. Known only from fourteen individuals, B. vincentia is distinguished by its semi-prostrate habit, with basally prostrate, distally ascending branches from the lignotuber, and distinctive perianth colouring. Its geographical location and ecological niche also separate it from its most similar congeners. Introduction The Banksia spinulosa complex has a complicated taxonomic history (Table 1). Smith (1793) first described and named B. spinulosa Sm., and subsequent botanists named two close relatives, B. collina R.Br. and B. -
CITES Norfolk Island Boobook Review
Original language: English AC28 Doc. 20.3.6 CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA ___________________ Twenty-eighth meeting of the Animals Committee Tel Aviv (Israel), 30 August-3 September 2015 Interpretation and implementation of the Convention Species trade and conservation Periodic review of species included in Appendices I and II (Resolution Conf 14.8 (Rev CoP16)) PERIODIC REVIEW OF NINOX NOVAESEELANDIAE UNDULATA 1. This document has been submitted by Australia.1 2. After the 25th meeting of the Animals Committee (Geneva, July 2011) and in response to Notification No. 2011/038, Australia committed to the evaluation of Ninox novaeseelandiae undulata as part of the Periodic review of the species included in the CITES Appendices. 3. This taxon is endemic to Australia. 4. Following our review of the status of this species, Australia recommends the transfer of Ninox novaeseelandiae undulata from CITES Appendix I to CITES Appendix II, in accordance with provisions of Resolution Conf. 9.24 (Rev CoP16), Annex 4 precautionary measure A.1. and A.2.a) i). 1 The geographical designations employed in this document do not imply the expression of any opinion whatsoever on the part of the CITES Secretariat (or the United Nations Environment Programme) concerning the legal status of any country, territory, or area, or concerning the delimitation of its frontiers or boundaries. The responsibility for the contents of the document rests exclusively with its author. AC28 Doc. 20.3.6 – p. 1 AC28 Doc. 20.3.6 Annex CoP17 Prop. xx CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA ____________________ DRAFT PROPOSAL TO AMEND THE APPENDICES (in accordance with Annex 4 to Resolution Conf. -
Proposal to Import Bombus Terestris Into
EXECUTIVE SUMMARY PROPOSAL TO IMPORT BOMBUS TERRESTRIS INTO MAINLAND AUSTRALIA FOR CROP POLLINATION PURPOSES PROPONENTS – AUSTRALIAN HYDROPONIC & GREENHOUSE ASSOCIATION PO BOX 538, NARRABEEN NSW PH: (03) 9939 5993 FAX: (03) 9939 5993 EMAIL: [email protected] WEBSITE: http://www.ahga.org.au Disclaimer This report was prepared by the Australian Hydroponic and Greenhouse Association. The material in it reflects the Association‟s best judgment on the information available to it at the time of preparation. Any use which a third party makes of this report, or any reliance on or decisions to be made based on it, are the responsibility of such third parties. The Australian Hydroponic & Greenhouse Association accepts no responsibility for damages, if any, suffered by any third party as a result of decisions made or actions based on this report. © This report is copyright 2008 and protected under the Berne Convention. Apart from any fair dealing for the purpose of private study, research, criticism or review, as permitted under the Copyright Act 1968, no part of this report may be reproduced in any form, including photocopying, microfilm, information storage and retrieval system, computer database, or software, or by any means, including electronic or mechanical, without the written permission of the Australian Hydroponic & Greenhouse Association. 1. The purpose and scope of the document This document is the culmination of over 10 years investigation into the proposed importation of a European bumblebee, Bombus terrestris, into Australia in managed hives for pollination purposes. While originally use in a wide range of field and greenhouse crops was envisaged, the proposal has been narrowed down to pollination of greenhouse crops, particularly tomatoes, in fully enclosed structures. -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
Creating Jobs, Protecting Forests?
Creating Jobs, Protecting Forests? An Analysis of the State of the Nation’s Regional Forest Agreements Creating Jobs, Protecting Forests? An Analysis of the State of the Nation’s Regional Forest Agreements The Wilderness Society. 2020, Creating Jobs, Protecting Forests? The State of the Nation’s RFAs, The Wilderness Society, Melbourne, Australia Table of contents 4 Executive summary Printed on 100% recycled post-consumer waste paper 5 Key findings 6 Recommendations Copyright The Wilderness Society Ltd 7 List of abbreviations All material presented in this publication is protected by copyright. 8 Introduction First published September 2020. 9 1. Background and legal status 12 2. Success of the RFAs in achieving key outcomes Contact: [email protected] | 1800 030 641 | www.wilderness.org.au 12 2.1 Comprehensive, Adequate, Representative Reserve system 13 2.1.1 Design of the CAR Reserve System Cover image: Yarra Ranges, Victoria | mitchgreenphotos.com 14 2.1.2 Implementation of the CAR Reserve System 15 2.1.3 Management of the CAR Reserve System 16 2.2 Ecologically Sustainable Forest Management 16 2.2.1 Maintaining biodiversity 20 2.2.2 Contributing factors to biodiversity decline 21 2.3 Security for industry 22 2.3.1 Volume of logs harvested 25 2.3.2 Employment 25 2.3.3 Growth in the plantation sector of Australia’s wood products industry 27 2.3.4 Factors contributing to industry decline 28 2.4 Regard to relevant research and projects 28 2.5 Reviews 32 3. Ability of the RFAs to meet intended outcomes into the future 32 3.1 Climate change 32 3.1.1 The role of forests in climate change mitigation 32 3.1.2 Climate change impacts on conservation and native forestry 33 3.2 Biodiversity loss/resource decline 33 3.2.1 Altered fire regimes 34 3.2.2 Disease 35 3.2.3 Pest species 35 3.3 Competing forest uses and values 35 3.3.1 Water 35 3.3.2 Carbon credits 36 3.4 Changing industries, markets and societies 36 3.5 International and national agreements 37 3.6 Legal concerns 37 3.7 Findings 38 4. -
Identifying Climate Refugia for Key Species in New South Wales - Final Report from the Bionode of the NSW Adaptation Hub
Identifying Climate Refugia for Key Species in New South Wales - Final Report from the BioNode of the NSW Adaptation Hub Linda J. Beaumont, John B. Baumgartner, Manuel Esperón-Rodríguez, David Nipperess 1 | P a g e Report prepared for the NSW Office of Environment and Heritage as part of a project funded by the NSW Adaptation Research Hub–Biodiversity Node. While every effort has been made to ensure all information within this document has been developed using rigorous scientific practice, readers should obtain independent advice before making any decision based on this information. Cite this publication as: Beaumont, L. J., Baumgartner, J. B., Esperón-Rodríguez, M, & Nipperess, D. (2019). Identifying climate refugia for key species in New South Wales - Final report from the BioNode of the NSW Adaptation Hub, Macquarie University, Sydney, Australia. For further correspondence contact: [email protected] 2 | P a g e Contents Acknowledgements ................................................................................................................................. 5 Abbreviations .......................................................................................................................................... 6 Glossary ................................................................................................................................................... 7 Executive summary ................................................................................................................................. 8 Highlights -
Approved Conservation Advice for Acacia Constablei (Narrabarba Wattle)
This Conservation Advice was approved by the Minister on 29 Apr 2014 Approved Conservation Advice for Acacia constablei (Narrabarba Wattle) (s266B of the Environment Protection and Biodiversity Conservation Act 1999) This Conservation Advice has been developed based on the best available information at the time this Conservation Advice was approved; this includes existing plans, records or management prescriptions for this species. Description Acacia constablei, Family Mimosaceae, also known as the Narrabarba Wattle, is an erect or spreading shrub or small tree with bipinnate leaves comprising 6–15 pairs of pinnae each with 9–30 pairs of pinnules (leaflets) 1.5–2.5 mm long and <1 mm wide (Harden, 2001). The pale yellow to white/cream flower heads are globular and 5–7 mm diameter (Harden, 2001). Individuals are mostly from 1 to 3 m high but can grow to 7 m in sheltered situations (Orchard and Wilson, 2001). Conservation Status Narrabarba Wattle is listed as vulnerable. This species is eligible for listing as vulnerable under the Environment Protection and Biodiversity Conservation Act 1999 (Cwlth) (EPBC Act) as, prior to the commencement of the EPBC Act, it was listed as vulnerable under Schedule 1 of the Endangered Species Protection Act 1992 (Cwlth). The Narrabarba Wattle is also listed as vulnerable under the Threatened Species Conservation Act 1995 (NSW). Distribution and Habitat Narrabarba Wattle has a geographic range of about 3 km (Briggs and Leigh, 1990) and is restricted to the Narrabarba area, on the far south coast of New South Wales (Tindale, 1980; Briggs and Leigh, 1990; Harden, 1991; Tame, 1992; Orchard and Wilson, 2001; NSW NPWS, 2003). -
Chapter 1: General Introduction and Aims
Margaret L. Stimpson Banksia spinulosa complex Chapter 1: General introduction and aims “The history of science, like the history of all human ideas, is a history of irresponsible dreams, of obstinacy, and of error. But science is one of the very few human activities perhaps the only one in which errors are systematically criticized and fairly often, in time, corrected. This is why we can say that, in science, we often learn from our mistakes, and why we can speak clearly and sensibly about making progress there.” (Popper 1963 p. 216) Proteaceae and Banksia The flowering plant family Proteaceae is predominantly distributed in the Southern Hemisphere and represents a classic Gondwanan clade, with fossils dating to c. 94 Mya, i.e., shortly after the separation of Africa from the rest of Gondwana (Guerin and Hill 2006). The family comprises about 80 genera with c. 1700 species, c.1450 of which are distributed in Australia and South Africa, which have the greatest concentrations of diversity (APG III 2009). There are also about 83 species in 8 genera in South and Central America (Prance and Plana 1998). Well known genera in the Proteaceae clade include Telopea, Protea, Banksia, Grevillea, Hakea, and Macadamia. The New South Wales floral emblem is the Waratah (Telopea speciosissima); Banksia, Grevillea, and Leucadendron are popular cut flowers, while the nuts of Macadamia integrifolia are widely grown commercially. The genus Banksia L.f. (Proteaceae subfam. Grevilleoideae) was first described on the basis of four species collected by Banks and Solander during the Cook voyage in 1770 (Thiele and Ladiges 1996; Collins et al. -
Endemic Species of Christmas Island, Indian Ocean D.J
RECORDS OF THE WESTERN AUSTRALIAN MUSEUM 34 055–114 (2019) DOI: 10.18195/issn.0312-3162.34(2).2019.055-114 Endemic species of Christmas Island, Indian Ocean D.J. James1, P.T. Green2, W.F. Humphreys3,4 and J.C.Z. Woinarski5 1 73 Pozieres Ave, Milperra, New South Wales 2214, Australia. 2 Department of Ecology, Environment and Evolution, La Trobe University, Melbourne, Victoria 3083, Australia. 3 Western Australian Museum, Locked Bag 49, Welshpool DC, Western Australia 6986, Australia. 4 School of Biological Sciences, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia 6009, Australia. 5 NESP Threatened Species Recovery Hub, Charles Darwin University, Casuarina, Northern Territory 0909, Australia, Corresponding author: [email protected] ABSTRACT – Many oceanic islands have high levels of endemism, but also high rates of extinction, such that island species constitute a markedly disproportionate share of the world’s extinctions. One important foundation for the conservation of biodiversity on islands is an inventory of endemic species. In the absence of a comprehensive inventory, conservation effort often defaults to a focus on the better-known and more conspicuous species (typically mammals and birds). Although this component of island biota often needs such conservation attention, such focus may mean that less conspicuous endemic species (especially invertebrates) are neglected and suffer high rates of loss. In this paper, we review the available literature and online resources to compile a list of endemic species that is as comprehensive as possible for the 137 km2 oceanic Christmas Island, an Australian territory in the north-eastern Indian Ocean. -
Urban Environments in Species Conservation Often Goes Unnoticed, and Must Be Better Recognised in Policy and Recovery Planning
This manuscript has been accepted for publication at Frontiers in Ecology and the Environment. The final, copy-edited and formatted article can be accessed via the journal, or by requesting a copy from the authors [email protected] or [email protected] Soanes and Lentini (2019) When cities are the last chance for saving species. Frontiers in Ecology and the Environment. https://doi.org/10.1002/fee.2032 When cities are the last chance for saving species Kylie Soanes1,2 and Pia E. Lentini2 1School of Ecosystem and Forest Sciences, The University of Melbourne, Parkville VIC Australia 3010 2School of BioSciences, The University of Melbourne, Parkville VIC Australia 3010 Corresponding author: Kylie Soanes, Email: [email protected] Running head: Saving urban-restricted species Manuscript type: Concepts and Questions Word count: 2838 (Not including title page or references) 1 Keywords: conservation, community stewardship, highly modified landscapes, novel habitats, species distributions, threatened species, urban planning, urban biodiversity. In a nutshell • Cities and towns can be important places for conservation and engaging people with nature • Urban areas can also be the last places that threatened species persist, and represent the last opportunity to save such species from extinction. • Conserving these urban-restricted threatened species requires looKing beyond conventional conservation reserves and embracing a variety of marginal habitats and land-use types • These species also benefit when community members are aware and engaged in local conservation action • The role of urban environments in species conservation often goes unnoticed, and must be better recognised in policy and recovery planning Abstract: Urban environments are arguably among the most fitting targets for conservation science: a golden opportunity to conserve species and ecosystems under threat, and allow people to engage with nature. -
Redalyc.ARE OUR ORCHIDS SAFE DOWN UNDER?
Lankesteriana International Journal on Orchidology ISSN: 1409-3871 [email protected] Universidad de Costa Rica Costa Rica BACKHOUSE, GARY N. ARE OUR ORCHIDS SAFE DOWN UNDER? A NATIONAL ASSESSMENT OF THREATENED ORCHIDS IN AUSTRALIA Lankesteriana International Journal on Orchidology, vol. 7, núm. 1-2, marzo, 2007, pp. 28- 43 Universidad de Costa Rica Cartago, Costa Rica Available in: http://www.redalyc.org/articulo.oa?id=44339813005 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative LANKESTERIANA 7(1-2): 28-43. 2007. ARE OUR ORCHIDS SAFE DOWN UNDER? A NATIONAL ASSESSMENT OF THREATENED ORCHIDS IN AUSTRALIA GARY N. BACKHOUSE Biodiversity and Ecosystem Services Division, Department of Sustainability and Environment 8 Nicholson Street, East Melbourne, Victoria 3002 Australia [email protected] KEY WORDS:threatened orchids Australia conservation status Introduction Many orchid species are included in this list. This paper examines the listing process for threatened Australia has about 1700 species of orchids, com- orchids in Australia, compares regional and national prising about 1300 named species in about 190 gen- lists of threatened orchids, and provides recommen- era, plus at least 400 undescribed species (Jones dations for improving the process of listing regionally 2006, pers. comm.). About 1400 species (82%) are and nationally threatened orchids. geophytes, almost all deciduous, seasonal species, while 300 species (18%) are evergreen epiphytes Methods and/or lithophytes. At least 95% of this orchid flora is endemic to Australia. -
Draft Survey Guidelines for Australia's Threatened Orchids
SURVEY GUIDELINES FOR AUSTRALIA’S THREATENED ORCHIDS GUIDELINES FOR DETECTING ORCHIDS LISTED AS ‘THREATENED’ UNDER THE ENVIRONMENT PROTECTION AND BIODIVERSITY CONSERVATION ACT 1999 0 Authorship and acknowledgements A number of experts have shared their knowledge and experience for the purpose of preparing these guidelines, including Allanna Chant (Western Australian Department of Parks and Wildlife), Allison Woolley (Tasmanian Department of Primary Industry, Parks, Water and Environment), Andrew Brown (Western Australian Department of Environment and Conservation), Annabel Wheeler (Australian Biological Resources Study, Australian Department of the Environment), Anne Harris (Western Australian Department of Parks and Wildlife), David T. Liddle (Northern Territory Department of Land Resource Management, and Top End Native Plant Society), Doug Bickerton (South Australian Department of Environment, Water and Natural Resources), John Briggs (New South Wales Office of Environment and Heritage), Luke Johnston (Australian Capital Territory Environment and Sustainable Development Directorate), Sophie Petit (School of Natural and Built Environments, University of South Australia), Melanie Smith (Western Australian Department of Parks and Wildlife), Oisín Sweeney (South Australian Department of Environment, Water and Natural Resources), Richard Schahinger (Tasmanian Department of Primary Industry, Parks, Water and Environment). Disclaimer The views and opinions contained in this document are not necessarily those of the Australian Government. The contents of this document have been compiled using a range of source materials and while reasonable care has been taken in its compilation, the Australian Government does not accept responsibility for the accuracy or completeness of the contents of this document and shall not be liable for any loss or damage that may be occasioned directly or indirectly through the use of or reliance on the contents of the document.