Stackhousia Pulvinaris (Alpine Candles) Alpine Candles
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Approved Conservation Advice for Stackhousia Annua (Annual Stackhousia)
This Conservation Advice was approved by the Minister / Delegate of the Minister on: 1/10/2008 Approved Conservation Advice (s266B of the Environment Protection and Biodiversity Conservation Act 1999) Approved Conservation Advice for Stackhousia annua (Annual Stackhousia) 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 Stackhousia annua, Family Stackhousiaceae, also known as Annual Stackhousia or Annual Candles, is a slender, erect, hairless annual growing to 19 cm (Barker, 1984). Leaves are 7– 25 mm long; basal leaves are narrowly spatulate and upper leaves are obovate (egg-shaped) to linear. Flowering occurs from September to October. The cream coloured flowers grow at the ends of stems in a dense, cylindrical floral spike (State Herbarium of South Australia, 2007). Conservation Status Annual Stackhousia 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). This species is also listed as vulnerable on the National Parks and Wildlife Act 1972 (South Australia). Distribution and Habitat Annual Stackhousia is endemic to near-coastal areas of south-west Yorke Peninsula and south-east Eyre Peninsula, South Australia (Barker, 1977; Barker, 1984; Pobke, 2007). This species was thought to occur in north-west Victoria and the South Australian mallee region (Walsh & Entwisle, 1999), but these records are now called a subspecies of Stackhousia aspericocca (Ross & Walsh, 2003). -
CANDOLLE, Prodr., XV, (1864)
The Genus Stackhousia in the Malay Archipelago by F.I. Brouwer (Botanical Laboratory of the University, Groningen, Netherlands). This publication is based on herbarium, materials which were kindly placed at the author’s disposal by the Directors of the Herbarium of the Buitenzorg Botanic Garden (B), the Leiden National Herbarium (L), the Herbarium of the Utrecht University (U), and the Herbarium of the Berlin-Dahlem Botanical Museum (BD), for whose kind help the author wishes to render his best thanks. Stackhousia SMITH, in Transact. Linn. Soc. London, IV (1798) 298. Most important literature: BENTHAM & HOOKER FIL., Gen. pi., I, 1 (1862) 371; BENTILAM, PL austr., I (1863) 404; in DE CANDOLLE, Prodr., XV, 1 (1864) 499; PAX, in ENGL. & PR., Nat. Pflanzenfam., ILL, 5 (1896) 233; BAILEY, Queensl. PL, I (1899) 263; PAMPANINI, in Bull. Herb. Boiss., ser. 2, V (1905) 912; VI (1906) tab. 13. Flowers regular, hermaphrodite. Calyx 5-merous, sepals usually more or less connate, rarely free. Corolla 5-merous, perigynous or nearly hypogynous; petals with long claws, rarely entirely free, usually free in the lower portion, connate in the upper portion of the claws; lobes 5, spreading, imbricate. Stamens 5, inserted on the margin of the calyx tube, free, usually different in length, included in the corolla tube. Ovary 2—5-, but usually 3-celled, each cell with one erect ana- tropous ovule; style with 2—5, usually 3, stigmatic lobes. Fruit with seed with 2—5, usually 3, one-seeded cocci and a central columella; membranous testa, fleshy albumen, straight embryo, short cotyledons, and inferior radicle. -
The Origin of the Bifurcating Style in Asteraceae (Compositae)
Annals of Botany 117: 1009–1021, 2016 doi:10.1093/aob/mcw033, available online at www.aob.oxfordjournals.org The origin of the bifurcating style in Asteraceae (Compositae) Liliana Katinas1,2,*, Marcelo P. Hernandez 2, Ana M. Arambarri2 and Vicki A. Funk3 1Division Plantas Vasculares, Museo de La Plata, La Plata, Argentina, 2Laboratorio de Morfologıa Comparada de Espermatofitas (LAMCE), Facultad de Ciencias Agrarias y Forestales, Universidad Nacional de La Plata, La Plata, Argentina and 3Department of Botany, NMNH, Smithsonian Institution, Washington D.C., USA *For correspondence. E-mail [email protected] Received: 20 November 2015 Returned for revision: 22 December 2015 Accepted: 8 January 2016 Published electronically: 20 April 2016 Background and Aims The plant family Asteraceae (Compositae) exhibits remarkable morphological variation in the styles of its members. Lack of studies on the styles of the sister families to Asteraceae, Goodeniaceae and Calyceraceae, obscures our understanding of the origin and evolution of this reproductive feature in these groups. The aim of this work was to perform a comparative study of style morphology and to discuss the relevance of im- portant features in the evolution of Asteraceae and its sister families. Methods The histochemistry, venation and general morphology of the styles of members of Goodeniaceae, Calyceraceae and early branching lineages of Asteraceae were analysed and put in a phylogenetic framework to dis- cuss the relevance of style features in the evolution of these families. Key Results The location of lipophilic substances allowed differentiation of receptive from non-receptive style papillae, and the style venation in Goodeniaceae and Calyceraceae proved to be distinctive. -
Plant Communities of Mt Barrow & Mt Barrow Falls
PLANT COMMUNITIES OF MT BARROW & MT BARROW FALLS John B. Davies Margaret J. Davies Consultant Queen Victoria and Art and Plomley Foundation II Mt Barrow J.B. & M.J. (1990) of Mt Barrow and Mt Barrow No.2 © Queen Victoria and Art Wellington St., Launceston,Tasmania 1990 CONTENTS ACKNOWLEDGEMENTS 3 BACKGROUND 4 SURVEY MT BARROW 11 OF MT BARROW PLANT COMMUNITIES 14 AND THEIR RESERVATION COMPARISON THE VEGETATION AT 30 BARROW AND LOMOND BOTANICAL OF MT BARROW RESERVE 31 DESCRIPTION THE COMMUNITIES BARROW FALLS THEIR APPENDIX 1 36 APPENDIX 2 MAP 3 39 APPENDIX 4 APPENDIX 5 APPENDIX 6 SPECIES 49 ACKNOWLEDGEMENTS Thanks are due to a number of people for assistance with this project. Firstly administrative assistance was by the Director of the Victoria Museum and Art Gallery, Mr Chris TasselL assistance was Michael Body, Kath Craig Reid and Mary Cameron. crt>''Y'it>,nt" are also due to Telecom for providing a key to the on the plateau, the Department of Lands, Parks and for providing a transparency base map of the area, and to Mr Mike Brouder and Mr John Harris Commission), for the use of 1 :20,000 colour aerial photographs of the area. Taxonomic was provided by Cameron (Honorary Research Associate, Queen Victoria Museum and Art Gallery) who also mounted all the plant collected, and various staff of the Tasmanian Herbarium particularly Mr Alex Dr Tony Orchard, Mr D. 1. Morris and Dr Winifred Curtis. thanks are due to Dr Brad Potts (Botany Department, of Tasmania) for assistance with data and table production and to Prof Kirkpatrick and Environmental ..J'U'U'~;'" of Tasmania) for the use and word-processing. -
First Steps Towards a Floral Structural Characterization of the Major Rosid Subclades
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2006 First steps towards a floral structural characterization of the major rosid subclades Endress, P K ; Matthews, M L Abstract: A survey of our own comparative studies on several larger clades of rosids and over 1400 original publications on rosid flowers shows that floral structural features support to various degrees the supraordinal relationships in rosids proposed by molecular phylogenetic studies. However, as many apparent relationships are not yet well resolved, the structural support also remains tentative. Some of the features that turned out to be of interest in the present study had not previously been considered in earlier supraordinal studies. The strongest floral structural support is for malvids (Brassicales, Malvales, Sapindales), which reflects the strong support of phylogenetic analyses. Somewhat less structurally supported are the COM (Celastrales, Oxalidales, Malpighiales) and the nitrogen-fixing (Cucurbitales, Fagales, Fabales, Rosales) clades of fabids, which are both also only weakly supported in phylogenetic analyses. The sister pairs, Cucurbitales plus Fagales, and Malvales plus Sapindales, are structurally only weakly supported, and for the entire fabids there is no clear support by the present floral structural data. However, an additional grouping, the COM clade plus malvids, shares some interesting features but does not appear as a clade in phylogenetic analyses. Thus it appears that the deepest split within eurosids- that between fabids and malvids - in molecular phylogenetic analyses (however weakly supported) is not matched by the present structural data. Features of ovules including thickness of integuments, thickness of nucellus, and degree of ovular curvature, appear to be especially interesting for higher level relationships and should be further explored. -
Report on the Grimwade Plant Collection of Percival St John and Botanical Exploration of Mt Buffalo National Park (Victoria, Australia)
Report on the Grimwade Plant Collection of Percival St John and Botanical Exploration of Mt Buffalo National Park (Victoria, Australia) Alison Kellow Michael Bayly Pauline Ladiges School of Botany, The University of Melbourne July, 2007 THE GRIMWADE PLANT COLLECTION, MT BUFFALO Contents Summary ...........................................................................................................................3 Mt Buffalo and its flora.....................................................................................................4 History of botanical exploration........................................................................................5 The Grimwade plant collection of Percival St John..........................................................8 A new collection of plants from Mt Buffalo - The Miegunyah Plant Collection (2006/2007) ....................................................................................................................................13 Plant species list for Mt Buffalo National Park...............................................................18 Conclusion.......................................................................................................................19 Acknowledgments...........................................................................................................19 References .......................................................................................................................20 Appendix 1 Details of specimens in the Grimwade Plant Collection.............................22 -
Taxonomic and Phylogenetic Census of the Celastrales: a Synthetic Review Shisode S.B.1 and D.A
Curr. Bot. 2(4): 36-43, 2011 REVIEW ARTICLE Taxonomic and phylogenetic census of the Celastrales: A synthetic review Shisode S.B.1 and D.A. Patil2 1 Department of Botany L. V. H. College, Panchavati, Nashik–422003 (M.S.) India 2 Post-Graduate Department of Botany S.S.V.P. Sanstha’s L.K.Dr.P.R.Ghogrey Science College, Dhule – 424 005, India K EYWORDS A BSTRACT Taxonomy, Phylogeny, Celastrales A comprehensive assessment of the taxonomic and phylogenetic status of the celeastralean plexus is presented. An attempt has been made to review synthetically C ORRESPONDENCE based on the data from different disciplines divulged by earlier authors and from present author’s study on the alliance. The taxonomic literature indicated that the D.A. Patil, Post-Graduate Department of Botany Celeastrales (sensu lato) are a loose-knit assemblage. The tribal, subfamilial, familial S.S.V.P. Sanstha’s L.K.Dr.P.R.Ghogrey Science and even ordinal boundaries are uncertain and even criss-cross each other. It College , Dhule – 424 005, India appeared that the alliance can be grouped under two taxonomic entities viz., the Celastrales and the Rhamnales which appear evolved convergently. E-mail: [email protected] E DITOR Datta Dhale CB Volume 2, Year 2011, Pages 36-43 Introduction Hipporcrateaceae are accorded an independent familial status. The order Celastrales (sensu lato) is a loose - knit The family Rhamnaceae is included under the Rhamnales assemblage. The taxonomic history clearly reflected that this alongwith the Vitaceae only. In the latest Engler's syllabus, alliance is not restricted to any taxonomic entity. -
On the Flora of Australia
L'IBRARY'OF THE GRAY HERBARIUM HARVARD UNIVERSITY. BOUGHT. THE FLORA OF AUSTRALIA, ITS ORIGIN, AFFINITIES, AND DISTRIBUTION; BEING AN TO THE FLORA OF TASMANIA. BY JOSEPH DALTON HOOKER, M.D., F.R.S., L.S., & G.S.; LATE BOTANIST TO THE ANTARCTIC EXPEDITION. LONDON : LOVELL REEVE, HENRIETTA STREET, COVENT GARDEN. r^/f'ORElGN&ENGLISH' <^ . 1859. i^\BOOKSELLERS^.- PR 2G 1.912 Gray Herbarium Harvard University ON THE FLORA OF AUSTRALIA ITS ORIGIN, AFFINITIES, AND DISTRIBUTION. I I / ON THE FLORA OF AUSTRALIA, ITS ORIGIN, AFFINITIES, AND DISTRIBUTION; BEIKG AN TO THE FLORA OF TASMANIA. BY JOSEPH DALTON HOOKER, M.D., F.R.S., L.S., & G.S.; LATE BOTANIST TO THE ANTARCTIC EXPEDITION. Reprinted from the JJotany of the Antarctic Expedition, Part III., Flora of Tasmania, Vol. I. LONDON : LOVELL REEVE, HENRIETTA STREET, COVENT GARDEN. 1859. PRINTED BY JOHN EDWARD TAYLOR, LITTLE QUEEN STREET, LINCOLN'S INN FIELDS. CONTENTS OF THE INTRODUCTORY ESSAY. § i. Preliminary Remarks. PAGE Sources of Information, published and unpublished, materials, collections, etc i Object of arranging them to discuss the Origin, Peculiarities, and Distribution of the Vegetation of Australia, and to regard them in relation to the views of Darwin and others, on the Creation of Species .... iii^ § 2. On the General Phenomena of Variation in the Vegetable Kingdom. All plants more or less variable ; rate, extent, and nature of variability ; differences of amount and degree in different natural groups of plants v Parallelism of features of variability in different groups of individuals (varieties, species, genera, etc.), and in wild and cultivated plants vii Variation a centrifugal force ; the tendency in the progeny of varieties being to depart further from their original types, not to revert to them viii Effects of cross-impregnation and hybridization ultimately favourable to permanence of specific character x Darwin's Theory of Natural Selection ; — its effects on variable organisms under varying conditions is to give a temporary stability to races, species, genera, etc xi § 3. -
John Stackhouse (1742-1819) and the Linnean Society
NEWSLETTER AND PROCEEDINGS OF THE LINNEAN SOCIETY OF LONDON VOLUME 24 • NUMBER 1 • JANUARY 2008 THE LINNEAN SOCIETY OF LONDON Registered Charity Number 220509 Burlington House, Piccadilly, London W1J 0BF Tel. (+44) (0)20 7434 4479; Fax: (+44) (0)20 7287 9364 e-mail: [email protected]; internet: www.linnean.org President Secretaries Council Professor David F Cutler BOTANICAL The Officers and Dr Sandra D Knapp Dr Pieter Baas Vice-Presidents Dr Andy Brown Professor Richard M Bateman ZOOLOGICAL Dr Joe Cain Dr Jenny M Edmonds Dr Vaughan R Southgate Dr John David Dr Sandy D Knapp Prof Peter S Davis Dr Vaughan R Southgate EDITORIAL Dr Shahina Ghazanfar Dr John R Edmondson Dr D J Nicholas Hind Treasurer Mr W M Alastair Land Professor Gren Ll Lucas OBE COLLECTIONS Dr D Tim J Littlewood Mrs Susan Gove Dr George McGavin Acting Executive Secretary Dr Malcolm Scoble Miss Gina Douglas Librarian & Archivist Prof Mark Seaward Miss Gina Douglas Dr Max Telford Head of Development Ms Elaine Shaughnessy Deputy Librarian Conservator Mrs Lynda Brooks Ms Janet Ashdown Financial Controller/Membership Mr Priya Nithianandan Assistant Librarian Special Publications Mr Ben Sherwood Manager Building and Office Manager Ms Leonie Berwick Ms Victoria Smith Communications Manager Ms Kate Longhurst THE LINNEAN Newsletter and Proceedings of the Linnean Society of London ISSN 0950-1096 Edited by Brian G Gardiner Editorial .......................................................................................................................2 Society News.............................................................................................................. -
Stackhousia Subterranea (Grassland Candles) Grassland Candles
Listing Statement for Stackhousia subterranea (grassland candles) grassland candles Stackhousia subterranea T A S M A N I A N T H R E A T E N E D F L O R A L I S T I N G S T A T E M E N T Image by H&A Wapstra Scientific name: Stackhousia subterranea W.R. Barker, J. Adelaide Bot. Gard. 21: 90 (2007) Family: Stackhousiaceae Common Name: grassland candles (Wapstra et al. 2005) Name History: Previously known in Tasmania as Stackhousia gunnii, Gunn's mignonette Status: Threatened Species Protection Act 1995 : endangered Environment Protection and Biodiversity Conservation Act 1999 : Not Listed Distribution: Endemic status: Not endemic to Tasmania Tasmanian NRM Regions: North and South Figure 1 . Distribution of Stackhousia subterranea in Plate 1. Stackhousia subterranea Tasmania. (Image by Oberon Carter). 1 Threatened Species Section – Department of Primary Industries & Water Listing Statement for Stackhousia subterranea (grassland candles) IDENTIFICATION AND ECOLOGY Confusing Species Stackhousia subterranea, until recently known in The genus Stackhousia is readily identifiable Tasmania as Stackhousia gunnii , is a single- when in flower due to its ‘candle-shaped’ stemmed hairless perennial herb in the inflorescence (Curtis & Morris 1975). The most Stackhousiaceae family. It grows 15 to 30 cm similar species to Stackhousia subterranea in high, with a few thick linear leaves near the Tasmania, Stackhousia monogyna , has stems that base. At the end of each stem there are deep- arise from a vertical taproot, thin leaves, and cream or yellowish tubular flowers arranged in floral bracts that are barely swollen at the base a candle-like spike. -
MAULES CREEK COAL PROJECT Biodiversity Offset Management Plan
MAULES CREEK COAL PROJECT Biodiversity Offset Management Plan For: Hansen Bailey December 2011 Final Draft PO Box 2474, Carlingford Court 2118 www.cumberlandecology.com.au Report No. 9125RP3 The preparation of this report has been in accordance with the brief provided by the Client and has relied upon the data and results collected at or under the times and conditions specified in the report. All findings, conclusions or recommendations contained within the report are based only on the aforementioned circumstances. The report has been prepared for use by the Client and no responsibility for its use by other parties is accepted by Cumberland Ecology. Revision Date Issued Reviewed by Approved by Date Approved Revision Type 1 David R David R 17/11/11 First draft 2 David R David R 22/11/11 Second draft 3 David R David R 30/11/11 Third draft 4 David R David R 01/12/11 Final Draft Approved by: David Robertson Position: Director Signed: Date: 1 December, 2011 MAULES CREEK COAL PROJECT FINAL DRAFT HANSEN BAILEY 1DECEMBER 2011 Table Of Contents 1 INTRODUCTION 1.1 Purpose 1.1 1.2 Background 1.1 1.2.1 Assessment and Approval Context 1.1 1.2.2 Description of the Impacts 1.2 1.2.3 Consistency with Recovery Plans and Conservation 1.3 Advices 1.2.4 Integration with Local Strategies 1.3 1.3 Aims and Objectives 1.3 1.4 Structure of the Biodiversity Offset Management Plan 1.4 1.5 Terms and Abbreviations 1.5 2 DESCRIPTION OF THE OFFSETS 2.1 General Description 2.1 2.1.1 Northern Offsets 2.1 2.1.2 Eastern and Western Offsets 2.6 2.1.3 Shared Offset Property -
BMC Evolutionary Biology Biomed Central
BMC Evolutionary Biology BioMed Central Research article Open Access Mitochondrial matR sequences help to resolve deep phylogenetic relationships in rosids Xin-Yu Zhu1,2, Mark W Chase3, Yin-Long Qiu4, Hong-Zhi Kong1, David L Dilcher5, Jian-Hua Li6 and Zhi-Duan Chen*1 Address: 1State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, the Chinese Academy of Sciences, Beijing 100093, China, 2Graduate University of the Chinese Academy of Sciences, Beijing 100039, China, 3Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, UK, 4Department of Ecology & Evolutionary Biology, The University Herbarium, University of Michigan, Ann Arbor, MI 48108-1048, USA, 5Florida Museum of Natural History, University of Florida, Gainesville, FL 32611-7800, USA and 6Arnold Arboretum of Harvard University, 125 Arborway, Jamaica Plain, MA 02130, USA Email: Xin-Yu Zhu - [email protected]; Mark W Chase - [email protected]; Yin-Long Qiu - [email protected]; Hong- Zhi Kong - [email protected]; David L Dilcher - [email protected]; Jian-Hua Li - [email protected]; Zhi- Duan Chen* - [email protected] * Corresponding author Published: 10 November 2007 Received: 19 June 2007 Accepted: 10 November 2007 BMC Evolutionary Biology 2007, 7:217 doi:10.1186/1471-2148-7-217 This article is available from: http://www.biomedcentral.com/1471-2148/7/217 © 2007 Zhu et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.