Biodiversity Conservation Act 2016
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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. -
Wedge-Tailed Shearwater Ardenna Pacifica Fallout Patterns Inform Targeted Management
Friswold et al.: Targeted management of Wedge-tailed Shearwater 245 WEDGE-TAILED SHEARWATER ARDENNA PACIFICA FALLOUT PATTERNS INFORM TARGETED MANAGEMENT BROOKE FRISWOLD1*, KEITH SWINDLE2, DAVID HYRENBACH3 & MELISSA R. PRICE1 1Department of Natural Resources & Environmental Management, University of Hawai‘i at Mˉanoa, 1910 East-West Rd., Honolulu, HI 96822, USA ([email protected]) 2United States Fish and Wildlife Service, 3375 Koapaka St., Honolulu, HI 96819, USA 3Hawai‘i Pacific University, 45-045 Kamehameha Hwy, Kˉane‘ohe, HI 96744, USA Received 17 January 2020, accepted 03 July 2020 ABSTRACT FRISWOLD, B., SWINDLE, K., HYRENBACH, D. & PRICE, M.R. 2020. Wedge-tailed Shearwater Ardenna pacifica fallout patterns inform targeted management. Marine Ornithology 48: 245–254. Seabird fledglings are often attracted to artificial, bright lights, leading to their grounding. This phenomenon is termed “fallout” and is associated with an increased risk of mortality from land-based threats. This study evaluated temporal trends and spatial factors, such as fallout clustering near lights and proximity to colonies, to inform targeted management actions. Standardized surveys were conducted from 2002 to 2010 for Wedge-tailed Shearwater Ardenna pacifica (WTSH) fallout on the island of O‘ahu, Hawai‘i, USA. First, yearly fallout counts along the transect showed a two-year cycle and identified 25 November as the date with the highest fallout across years. Second, artificial lights and utility lines were present in 94% and 83% of fallout locations, leading to significantly higher fallout rates at these locations compared to random points along the transect. Third, fallout decreased significantly as the distance from the colonies increased and was negligible farther than 5 km from the nearest colony. -
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Vol. 651: 163–181, 2020 MARINE ECOLOGY PROGRESS SERIES Published October 1 https://doi.org/10.3354/meps13439 Mar Ecol Prog Ser OPEN ACCESS Habitat preferences, foraging behaviour and bycatch risk among breeding sooty shearwaters Ardenna grisea in the Southwest Atlantic Anne-Sophie Bonnet-Lebrun1,2,3,8,*, Paulo Catry1, Tyler J. Clark4,9, Letizia Campioni1, Amanda Kuepfer5,6,7, Megan Tierny6, Elizabeth Kilbride4, Ewan D. Wakefield4 1MARE − Marine and Environmental Sciences Centre, ISPA - Instituto Universitário, Rua Jardim do Tabaco 34, 1149-041 Lisboa, Portugal 2Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK 3Centre d’Ecologie Fonctionnelle et Evolutive CEFE UMR 5175, CNRS — Université de Montpellier - Université Paul-Valéry Montpellier — EPHE, 34293 Montpellier cedex 5, France 4Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow G12 8QQ, UK 5FIFD — Falkland Islands Fisheries Department, Falkland Islands Government, PO Box 598, Stanley, Falkland Islands, FIQQ 1ZZ, UK 6SAERI — South Atlantic Environmental Research Institute, Stanley, Falkland Islands, FIQQ 1ZZ, UK 7Environment and Sustainability Institute, University of Exeter, Penryn Campus, Penryn TR10 9FE, UK 8Present address: British Antarctic Survey, High Cross, Madingley Road, Cambridge CB4 0ET, UK 9Present address: Wildlife Biology Program, Department of Ecosystem and Conservation Sciences, W.A. Franke College of Forestry and Conservation, University of Montana, 32 Campus Drive, Missoula, Montana 59812, USA ABSTRACT: Pelagic seabirds are important components of many marine ecosystems. The most abundant species are medium/small sized petrels (<1100 g), yet the sub-mesoscale (<10 km) distri- bution, habitat use and foraging behaviour of this group are not well understood. Sooty shearwaters Ardenna grisea are among the world’s most numerous pelagic seabirds. -
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. -
The First Chloroplast Genome Sequence of Boswellia Sacra, a Resin-Producing Plant in Oman
RESEARCH ARTICLE The First Chloroplast Genome Sequence of Boswellia sacra, a Resin-Producing Plant in Oman Abdul Latif Khan1, Ahmed Al-Harrasi1*, Sajjad Asaf2, Chang Eon Park2, Gun-Seok Park2, Abdur Rahim Khan2, In-Jung Lee2, Ahmed Al-Rawahi1, Jae-Ho Shin2* 1 UoN Chair of Oman's Medicinal Plants & Marine Natural Products, University of Nizwa, Nizwa, Oman, 2 School of Applied Biosciences, Kyungpook National University, Daegu, Republic of Korea a1111111111 * [email protected] (AAH); [email protected] (JHS) a1111111111 a1111111111 a1111111111 Abstract a1111111111 Boswellia sacra (Burseraceae), a keystone endemic species, is famous for the production of fragrant oleo-gum resin. However, the genetic make-up especially the genomic informa- tion about chloroplast is still unknown. Here, we described for the first time the chloroplast OPEN ACCESS (cp) genome of B. sacra. The complete cp sequence revealed a circular genome of 160,543 Citation: Khan AL, Al-Harrasi A, Asaf S, Park CE, bp size with 37.61% GC content. The cp genome is a typical quadripartite chloroplast struc- Park G-S, Khan AR, et al. (2017) The First ture with inverted repeats (IRs 26,763 bp) separated by small single copy (SSC; 18,962 bp) Chloroplast Genome Sequence of Boswellia sacra, and large single copy (LSC; 88,055 bp) regions. De novo assembly and annotation showed a Resin-Producing Plant in Oman. PLoS ONE 12 the presence of 114 unique genes with 83 protein-coding regions. The phylogenetic analysis (1): e0169794. doi:10.1371/journal.pone.0169794 revealed that the B. sacra cp genome is closely related to the cp genome of Azadirachta Editor: Xiu-Qing Li, Agriculture and Agri-Food indica and Citrus sinensis, while most of the syntenic differences were found in the non-cod- Canada, CANADA ing regions. -
The Relationships of the Starlings (Sturnidae: Sturnini) and the Mockingbirds (Sturnidae: Mimini)
THE RELATIONSHIPS OF THE STARLINGS (STURNIDAE: STURNINI) AND THE MOCKINGBIRDS (STURNIDAE: MIMINI) CHARLESG. SIBLEYAND JON E. AHLQUIST Departmentof Biologyand PeabodyMuseum of Natural History,Yale University, New Haven, Connecticut 06511 USA ABSTRACT.--OldWorld starlingshave been thought to be related to crowsand their allies, to weaverbirds, or to New World troupials. New World mockingbirdsand thrashershave usually been placed near the thrushesand/or wrens. DNA-DNA hybridization data indi- cated that starlingsand mockingbirdsare more closelyrelated to each other than either is to any other living taxon. Some avian systematistsdoubted this conclusion.Therefore, a more extensiveDNA hybridizationstudy was conducted,and a successfulsearch was made for other evidence of the relationshipbetween starlingsand mockingbirds.The resultssup- port our original conclusionthat the two groupsdiverged from a commonancestor in the late Oligoceneor early Miocene, about 23-28 million yearsago, and that their relationship may be expressedin our passerineclassification, based on DNA comparisons,by placing them as sistertribes in the Family Sturnidae,Superfamily Turdoidea, Parvorder Muscicapae, Suborder Passeres.Their next nearest relatives are the members of the Turdidae, including the typical thrushes,erithacine chats,and muscicapineflycatchers. Received 15 March 1983, acceptedI November1983. STARLINGS are confined to the Old World, dine thrushesinclude Turdus,Catharus, Hylocich- mockingbirdsand thrashersto the New World. la, Zootheraand Myadestes.d) Cinclusis -
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. -
Jungle Myna (Acridotheres Fuscus)
Invasive animal risk assessment Biosecurity Queensland Agriculture Fisheries and Department of Jungle myna Acridotheres fuscus Steve Csurhes First published 2011 Updated 2016 © State of Queensland, 2016. 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. You must keep intact the copyright notice and attribute the State of Queensland as the source of the publication. Note: Some content in this publication may have different licence terms as indicated. For more information on this licence visit http://creativecommons.org/licenses/by/3.0/au/ deed.en" http://creativecommons.org/licenses/by/3.0/au/deed.en Front cover: Jungle myna Photo: Used with permission, Wikimedia Commons. Invasive animal risk assessment: Jungle myna Acridotheres fuscus 2 Contents Summary 4 Introduction 5 Identity and taxonomy 5 Description and biology 5 Diet 5 Reproduction 5 Preferred habitat and climate 6 Native range and global distribution 6 Current distribution and impact in Queensland 6 History as a pest overseas 7 Use 7 Potential distribution and impact in Queensland 7 References 8 Invasive animal risk assessment: Jungle myna Acridotheres fuscus 3 Summary Acridotheres fuscus (jungle myna) is native to an extensive area of India and parts of southeast Asia. Naturalised populations exist in Singapore, Taiwan, Fiji, Western Samoa and elsewhere. In Fiji, the species occasionally causes significant damage to crops of ground nuts, with crop losses of up to 40% recorded. Within its native range (South India), it is not a well documented pest, but occasionally causes considerable (localised) damage to fruit orchards.