Tarwin Lower Cemetery Plant List
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2020 Majura Ainslie Plant List.Xlsx
Plant Species List for Mount Majura and Mount Ainslie, Canberra Base data from Ingwerson, F; O. Evans & B. Griffiths. (1974). Vegetation of the Ainslie-Majura Reserve . Conservation Series No. 2. AGPS Canberra. Re-organised, revised and updated by Michael Doherty, CSIRO Ecosystem Sciences and Waltraud Pix, Friends of Mt. Majura With advice from Isobel Crawford, Australian Botanical Surveys Current version of 01.10.2020 Names: Census of Plants of the Australian Capital Territory, Version 4.1, 2019 Enquiries:Version 3.0 [email protected] (8th June 2012) subsp. = subspecies Form ? = questionable status or identity f = herb, forb sp. aff. = having close affinities with i.e. similar but not quite the sameo = herb, orchid syn. = synonymous with i.e. most recent previous name, or alternativeg = nameherb, grass sens. lat. = in the broad sense of the species concept gl = herb, grass- or sedge-like var. = variety s = shrub (including creeper and climber) sp. = species i.e. identity yet to be finalised st = shrub / small tree spp. = species in the plural i.e. more than one species t = tree MM Mount Majura. Notionally north of “Blue Metal” Road; MA Mount Ainslie. Notionally south of “Blue Metal” Road (VVV) Species occurrence checking; currently focused on Mt. Majura rather than Mt. Ainslie. No ticks next to name = species reported but not yet confirmed for Mt Majura and Mt Ainslie. Status is locally native except for: PE = Planted Exotic PN = Planted Non-local Native WE = Weed Exotic WN = Weed Non-local Native ‘Planted’ status refers to individuals which are planted but not spreading ‘Weed’ status refers to species reproducing in the wild Scientific name Common name MM MA Status Form Family Isolepis sp . -
List of Plants Observed and Identified by Members of the Ringwood Field Naturalists Club Inc
LIST OF PLANTS OBSERVED AND IDENTIFIED BY MEMBERS OF THE RINGWOOD FIELD NATURALISTS CLUB INC. ON THEIR SPRING FIELD TRIP TO YARRAM 16-18 NOVEMBER 2012 COMPILED BY JUDITH V COOKE Ninety Mile Beach 17 11 2012 1 Map of Yarram and surrounding places visited 16-18 11 2012 2 3 Botanical Name Common Name 16 17 18 11 11 11 ORCHIDS Caladenia carnea Pink Fingers F Caladenia gracilis Musky Caladenia F Caleana major Flying Duck Orchid F Calochilus campestris Copper Beard Orchid F Chiloglottis cornuta Little Bird Orchid F Chiloglottis valida Common Bird Orchid F Diuris sulphurea Hornet Orchid F F Microtis sp Onion Orchid F Stegostyla transitoria Eastern Bronze Caladenia F Thelymitra ixiodes Spotted Sun Orchid F Thelymitra media Tall Sun Orchid F 4 5 Botanical Name Common Name 16 17 18 11 11 11 FERNS Asplenium bulbiferum Mother Spleenwort Blechnum chambersii Lance Water Fern Blechnum fluviatile Ray Water Fern Blechnum nudum Fishbone Water Fern Blechnum patersonii Strap Water Fern Blechnum wattsii Hard Water Fern Calochlaena dubia Common Ground Fern Cyathea australis Rough Tree Fern Dicksonia antarctica Soft Tree Fern Grammitis billardieri Finger Fern Histiopteris incisa Batswing Fern Hymenophyllum cupressiforme Common Filmy Fern Hymenophyllum sp? Filmy Fern Hymenophyllum sp? Filmy/Bristle Fern Lastreopsis acuminata Shiny Shield Fern Microsorum diversifolium Kangaroo Fern Polystichum proliferum Mother Shield Fern Pteridium esculentum Austral Bracken Rumohra adiantiformis Shield Hare's-foot 6 Botanical Name Common Name 16 17 18 -
LCSH Section L
L (The sound) Formal languages La Boderie family (Not Subd Geog) [P235.5] Machine theory UF Boderie family BT Consonants L1 algebras La Bonte Creek (Wyo.) Phonetics UF Algebras, L1 UF LaBonte Creek (Wyo.) L.17 (Transport plane) BT Harmonic analysis BT Rivers—Wyoming USE Scylla (Transport plane) Locally compact groups La Bonte Station (Wyo.) L-29 (Training plane) L2TP (Computer network protocol) UF Camp Marshall (Wyo.) USE Delfin (Training plane) [TK5105.572] Labonte Station (Wyo.) L-98 (Whale) UF Layer 2 Tunneling Protocol (Computer network BT Pony express stations—Wyoming USE Luna (Whale) protocol) Stagecoach stations—Wyoming L. A. Franco (Fictitious character) BT Computer network protocols La Borde Site (France) USE Franco, L. A. (Fictitious character) L98 (Whale) USE Borde Site (France) L.A.K. Reservoir (Wyo.) USE Luna (Whale) La Bourdonnaye family (Not Subd Geog) USE LAK Reservoir (Wyo.) LA 1 (La.) La Braña Region (Spain) L.A. Noire (Game) USE Louisiana Highway 1 (La.) USE Braña Region (Spain) UF Los Angeles Noire (Game) La-5 (Fighter plane) La Branche, Bayou (La.) BT Video games USE Lavochkin La-5 (Fighter plane) UF Bayou La Branche (La.) L.C.C. (Life cycle costing) La-7 (Fighter plane) Bayou Labranche (La.) USE Life cycle costing USE Lavochkin La-7 (Fighter plane) Labranche, Bayou (La.) L.C. Smith shotgun (Not Subd Geog) La Albarrada, Battle of, Chile, 1631 BT Bayous—Louisiana UF Smith shotgun USE Albarrada, Battle of, Chile, 1631 La Brea Avenue (Los Angeles, Calif.) BT Shotguns La Albufereta de Alicante Site (Spain) This heading is not valid for use as a geographic L Class (Destroyers : 1939-1948) (Not Subd Geog) USE Albufereta de Alicante Site (Spain) subdivision. -
Cassytha Pubescens
Cassytha pubescens: Germination biology and interactions with native and introduced hosts Hong Tai (Steven), Tsang B.Sc. Hons (University of Adelaide) Thesis submitted for the degree of Master of Science School of Earth & Environmental Science University of Adelaide, Australia 03/05/2010 i Table of Contents Table of Contents ........................................................................................................... ii Abstract .......................................................................................................................... v Declaration ................................................................................................................... vii Acknowledgements .................................................................................................... viii Chapter. 1 Introduction .................................................................................................. 1 1.1 General Introduction ............................................................................................ 1 1.2 Literature Review ................................................................................................. 3 1.2.1 Characteristics of parasitic control agents .................................................... 3 1.2.2. Direct impacts on hosts ................................................................................ 7 1.2.3. Indirect impacts on hosts ............................................................................. 8 1.2.4. Summary ................................................................................................... -
Loranthaceae1
Flora of South Australia 5th Edition | Edited by Jürgen Kellermann LORANTHACEAE1 P.J. Lang2 & B.A. Barlow3 Aerial hemi-parasitic shrubs on branches of woody plants attached by haustoria; leaves mostly opposite, entire. Inflorescence terminal or lateral; flowers bisexual; calyx reduced to an entire, lobed or toothed limb at the apex of the ovary, without vascular bundles; corolla free or fused, regular or slightly zygomorphic, 4–6-merous, valvate; stamens as many as and opposite the petals, epipetalous, anthers 2- or 4-locular, mostly basifixed, immobile, introrse and continuous with the filament but sometimes dorsifixed and then usually versatile, opening by longitudinal slits; pollen trilobate; ovary inferior, without differentiated locules or ovules. Fruit berry-like; seed single, surrounded by a copious viscous layer. Mistletoes. 73 genera and around 950 species widely distributed in the tropics and south temperate regions with a few species in temperate Asia and Europe. Australia has 12 genera (6 endemic) and 75 species. Reference: Barlow (1966, 1984, 1996), Nickrent et al. (2010), Watson (2011). 1. Petals free 2. Anthers basifixed, immobile, introrse; inflorescence axillary 3. Inflorescence not subtended by enlarged bracts more than 20 mm long ....................................... 1. Amyema 3: Inflorescence subtended by enlarged bracts more than 20 mm long which enclose the buds prior to anthesis ......................................................................................................................... 2. Diplatia 2: Anthers dorsifixed, versatile; inflorescence terminal ........................................................................... 4. Muellerina 1: Petals united into a curved tube, more deeply divided on the concave side ................................................ 3. Lysiana 1. AMYEMA Tiegh. Bull. Soc. Bot. France 41: 499 (1894). (Greek a-, negative; myeo, I instruct, initiate; referring to the genus being not previously recognised; cf. -
Phylogenetic Relationships of Discyphus Scopulariae
Phytotaxa 173 (2): 127–139 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2014 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.173.2.3 Phylogenetic relationships of Discyphus scopulariae (Orchidaceae, Cranichideae) inferred from plastid and nuclear DNA sequences: evidence supporting recognition of a new subtribe, Discyphinae GERARDO A. SALAZAR1, CÁSSIO VAN DEN BERG2 & ALEX POPOVKIN3 1Departamento de Botánica, Instituto de Biología, Universidad Nacional Autónoma de México, Apartado Postal 70-367, 04510 México, Distrito Federal, México; E-mail: [email protected] 2Universidade Estadual de Feira de Santana, Departamento de Ciências Biológicas, Av. Transnordestina s.n., 44036-900, Feira de Santana, Bahia, Brazil 3Fazenda Rio do Negro, Entre Rios, Bahia, Brazil Abstract The monospecific genus Discyphus, previously considered a member of Spiranthinae (Orchidoideae: Cranichideae), displays both vegetative and floral morphological peculiarities that are out of place in that subtribe. These include a single, sessile, cordate leaf that clasps the base of the inflorescence and lies flat on the substrate, petals that are long-decurrent on the column, labellum margins free from sides of the column and a column provided with two separate, cup-shaped stigmatic areas. Because of its morphological uniqueness, the phylogenetic relationships of Discyphus have been considered obscure. In this study, we analyse nucleotide sequences of plastid and nuclear DNA under maximum parsimony -
Variation of Physical Seed Dormancy and Its Ecological Role in Fire-Prone Ecosystems
University of Wollongong Research Online University of Wollongong Thesis Collection 1954-2016 University of Wollongong Thesis Collections 2016 Variation of physical seed dormancy and its ecological role in fire-prone ecosystems Ganesha Sanjeewani Liyanage Borala Liyanage University of Wollongong Follow this and additional works at: https://ro.uow.edu.au/theses University of Wollongong Copyright Warning You may print or download ONE copy of this document for the purpose of your own research or study. The University does not authorise you to copy, communicate or otherwise make available electronically to any other person any copyright material contained on this site. You are reminded of the following: This work is copyright. Apart from any use permitted under the Copyright Act 1968, no part of this work may be reproduced by any process, nor may any other exclusive right be exercised, without the permission of the author. Copyright owners are entitled to take legal action against persons who infringe their copyright. A reproduction of material that is protected by copyright may be a copyright infringement. A court may impose penalties and award damages in relation to offences and infringements relating to copyright material. Higher penalties may apply, and higher damages may be awarded, for offences and infringements involving the conversion of material into digital or electronic form. Unless otherwise indicated, the views expressed in this thesis are those of the author and do not necessarily represent the views of the University of Wollongong. Recommended Citation Borala Liyanage, Ganesha Sanjeewani Liyanage, Variation of physical seed dormancy and its ecological role in fire-prone ecosystems, Doctor of Philosophy thesis, School of Biological Sciences, University of Wollongong, 2016. -
Comparative Floral Presentation and Bee-Pollination in Two Sprengelia Species (Ericaceae)
Comparative floral presentation and bee-pollination in two Sprengelia species (Ericaceae) Karen A. Johnson* and Peter B. McQuillan School of Geography and Environmental Studies, University of Tasmania, Private Bag 78, Hobart, Tasmania 7001, Australia. *Corresponding author. E-mail: [email protected] Abstract: Pollination by sonication is unusual in the Styphelioideae, family Ericaceae. Sprengelia incarnata and Sprengelia propinqua have floral characteristics that suggested they might be adapted to buzz pollination.Both species have florally similar nectarless flowers except that the stamens ofSprengelia propinqua spread widely after the flower opens, while those of Sprengelia incarnata cohere in the centre of the flower. To test whether sonication occurs, we observed bee behaviour at the flowers of both plant species, documented potential pollinators, and examined their floral and pollen attributes. We found that Sprengelia incarnata had smaller and drier pollen than Sprengelia propinqua. We found that Sprengelia incarnata was sonicated by native bees in the families Apidae (Exoneura), Halictidae (Lasioglossum) and Colletidae (Leioproctus, Euryglossa). Sprengelia propinqua was also visited by bees from the Apidae (Exoneura) and Halictidae (Lasioglossum), but pollen was collected by scraping. The introduced Apis mellifera (Apidae) foraged at Sprengelia propinqua but ignored Sprengelia incarnata. The two Sprengelia species shared some genera of potential pollinators, but appeared to have diverged enough in their floral and pollen characters to elicit different behaviours from the native and introduced bees. Cunninghamia (2011) 12 (1): 45–51 Introduction species, some Leucopogon species, Richea milliganii (Hook.f.) F.Muell., and Sprengelia incarnata Sm. (Houston The interactions between plants and pollinators are thought & Ladd, 2002; Ladd, 2006). -
Jervis Bay Territory Page 1 of 50 21-Jan-11 Species List for NRM Region (Blank), Jervis Bay Territory
Biodiversity Summary for NRM Regions Species List What is the summary for and where does it come from? This list has been produced by the Department of Sustainability, Environment, Water, Population and Communities (SEWPC) for the Natural Resource Management Spatial Information System. The list was produced using the AustralianAustralian Natural Natural Heritage Heritage Assessment Assessment Tool Tool (ANHAT), which analyses data from a range of plant and animal surveys and collections from across Australia to automatically generate a report for each NRM region. Data sources (Appendix 2) include national and state herbaria, museums, state governments, CSIRO, Birds Australia and a range of surveys conducted by or for DEWHA. For each family of plant and animal covered by ANHAT (Appendix 1), this document gives the number of species in the country and how many of them are found in the region. It also identifies species listed as Vulnerable, Critically Endangered, Endangered or Conservation Dependent under the EPBC Act. A biodiversity summary for this region is also available. For more information please see: www.environment.gov.au/heritage/anhat/index.html Limitations • ANHAT currently contains information on the distribution of over 30,000 Australian taxa. This includes all mammals, birds, reptiles, frogs and fish, 137 families of vascular plants (over 15,000 species) and a range of invertebrate groups. Groups notnot yet yet covered covered in inANHAT ANHAT are notnot included included in in the the list. list. • The data used come from authoritative sources, but they are not perfect. All species names have been confirmed as valid species names, but it is not possible to confirm all species locations. -
Intro Outline
THE REPRODUCTIVE ECOLOGY OF TWO TERRESTRIAL ORCHIDS, CALADENIA RIGIDA AND CALADENIA TENTACULATA RENATE FAAST Submitted for the degree of Doctor of Philosophy School of Earth and Environmental Sciences The University of Adelaide, South Australia December, 2009 i . DEcLARATION This work contains no material which has been accepted for the award of any other degree or diploma in any university or other tertiary institution to Renate Faast and, to the best of my knowledge and belief, contains no material previously published or written by another person, except where due reference has been made in the text. I give consent to this copy of my thesis when deposited in the University Library, being made available for loan and photocopying, subject to the provisions of the Copyright Act 1968. The author acknowledges that copyright of published works contained within this thesis (as listed below) resides with the copyright holder(s) of those works. I also give permission for the digital version of my thesis to be made available on the web, via the University's digital research repository, the Library catalogue, the Australasian Digital Theses Program (ADTP) and also through web search engines. Published works contained within this thesis: Faast R, Farrington L, Facelli JM, Austin AD (2009) Bees and white spiders: unravelling the pollination' syndrome of C aladenia ri gída (Orchidaceae). Australian Joumal of Botany 57:315-325. Faast R, Facelli JM (2009) Grazrngorchids: impact of florivory on two species of Calademz (Orchidaceae). Australian Journal of Botany 57:361-372. Farrington L, Macgillivray P, Faast R, Austin AD (2009) Evaluating molecular tools for Calad,enia (Orchidaceae) species identification. -
Introduction Methods Results
Papers and Proceedings Royal Society ofTasmania, Volume 1999 103 THE CHARACTERISTICS AND MANAGEMENT PROBLEMS OF THE VEGETATION AND FLORA OF THE HUNTINGFIELD AREA, SOUTHERN TASMANIA by J.B. Kirkpatrick (with two tables, four text-figures and one appendix) KIRKPATRICK, J.B., 1999 (31:x): The characteristics and management problems of the vegetation and flora of the Huntingfield area, southern Tasmania. Pap. Proc. R. Soc. Tasm. 133(1): 103-113. ISSN 0080-4703. School of Geography and Environmental Studies, University ofTasmania, GPO Box 252-78, Hobart, Tasmania, Australia 7001. The Huntingfield area has a varied vegetation, including substantial areas ofEucalyptus amygdalina heathy woodland, heath, buttongrass moorland and E. amygdalina shrubbyforest, with smaller areas ofwetland, grassland and E. ovata shrubbyforest. Six floristic communities are described for the area. Two hundred and one native vascular plant taxa, 26 moss species and ten liverworts are known from the area, which is particularly rich in orchids, two ofwhich are rare in Tasmania. Four other plant species are known to be rare and/or unreserved inTasmania. Sixty-four exotic plantspecies have been observed in the area, most ofwhich do not threaten the native biodiversity. However, a group offire-adapted shrubs are potentially serious invaders. Management problems in the area include the maintenance ofopen areas, weed invasion, pathogen invasion, introduced animals, fire, mechanised recreation, drainage from houses and roads, rubbish dumping and the gathering offirewood, sand and plants. Key Words: flora, forest, heath, Huntingfield, management, Tasmania, vegetation, wetland, woodland. INTRODUCTION species with the most cover in the shrub stratum (dominant species) was noted. If another species had more than half The Huntingfield Estate, approximately 400 ha of forest, the cover ofthe dominant one it was noted as a codominant. -
Plant Life of Western Australia
INTRODUCTION The characteristic features of the vegetation of Australia I. General Physiography At present the animals and plants of Australia are isolated from the rest of the world, except by way of the Torres Straits to New Guinea and southeast Asia. Even here adverse climatic conditions restrict or make it impossible for migration. Over a long period this isolation has meant that even what was common to the floras of the southern Asiatic Archipelago and Australia has become restricted to small areas. This resulted in an ever increasing divergence. As a consequence, Australia is a true island continent, with its own peculiar flora and fauna. As in southern Africa, Australia is largely an extensive plateau, although at a lower elevation. As in Africa too, the plateau increases gradually in height towards the east, culminating in a high ridge from which the land then drops steeply to a narrow coastal plain crossed by short rivers. On the west coast the plateau is only 00-00 m in height but there is usually an abrupt descent to the narrow coastal region. The plateau drops towards the center, and the major rivers flow into this depression. Fed from the high eastern margin of the plateau, these rivers run through low rainfall areas to the sea. While the tropical northern region is characterized by a wet summer and dry win- ter, the actual amount of rain is determined by additional factors. On the mountainous east coast the rainfall is high, while it diminishes with surprising rapidity towards the interior. Thus in New South Wales, the yearly rainfall at the edge of the plateau and the adjacent coast often reaches over 100 cm.