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Draft Recovery Plan for Quassia Sp
Draft NSW & National Recovery Plan Quassia sp. B (Moonee Quassia) August 2004 © NSW Department of Environment and Conservation, 2004. This work is copyright. However, material presented in this plan may be copied for personal use or published for educational purposes, providing that any extracts are fully acknowledged. Apart from this and any other use as permitted under the Copyright Act 1968 (NSW), no part may be reproduced without prior written permission from NSW Department of Environment and Conservation. NSW Department of Environment and Conservation 43 Bridge Street (PO Box 1967) Hurstville NSW 2220 Tel: 02 9585 6444 www.nationalparks.nsw.gov.au Requests for information or comments regarding the recovery program for the Moonee Quassia are best directed to: The Moonee Quassia Recovery Co-ordinator Threatened Species Unit, North East Branch NSW Department of Environment and Conservation Locked Bag 914 Coffs Harbour NSW 2450 Tel: 02 6651 5946 Cover illustrator: Liesel Yates This plan should be cited as follows: NSW Department of Environment and Conservation 2004, Draft Recovery Plan for Quassia sp. B (Moonee Quassia), NSW Department of Environment and Conservation, Hurstville. ISBN 07313 69270 Draft Recovery Plan The Moonee Quassia Draft Recovery Plan for Quassia sp. B (Moonee Quassia). Foreword The New South Wales Government established a new environment agency on 24 September 2003, the Department of Environment and Conservation, which incorporates the New South Wales National Parks and Wildlife Service. Responsibility for the preparation of Recovery Plans now rests with this new department. This document, when finalised, will constitute the formal National and New South Wales State Recovery Plan for Quassia sp. -
Alphabetical Lists of the Vascular Plant Families with Their Phylogenetic
Colligo 2 (1) : 3-10 BOTANIQUE Alphabetical lists of the vascular plant families with their phylogenetic classification numbers Listes alphabétiques des familles de plantes vasculaires avec leurs numéros de classement phylogénétique FRÉDÉRIC DANET* *Mairie de Lyon, Espaces verts, Jardin botanique, Herbier, 69205 Lyon cedex 01, France - [email protected] Citation : Danet F., 2019. Alphabetical lists of the vascular plant families with their phylogenetic classification numbers. Colligo, 2(1) : 3- 10. https://perma.cc/2WFD-A2A7 KEY-WORDS Angiosperms family arrangement Summary: This paper provides, for herbarium cura- Gymnosperms Classification tors, the alphabetical lists of the recognized families Pteridophytes APG system in pteridophytes, gymnosperms and angiosperms Ferns PPG system with their phylogenetic classification numbers. Lycophytes phylogeny Herbarium MOTS-CLÉS Angiospermes rangement des familles Résumé : Cet article produit, pour les conservateurs Gymnospermes Classification d’herbier, les listes alphabétiques des familles recon- Ptéridophytes système APG nues pour les ptéridophytes, les gymnospermes et Fougères système PPG les angiospermes avec leurs numéros de classement Lycophytes phylogénie phylogénétique. Herbier Introduction These alphabetical lists have been established for the systems of A.-L de Jussieu, A.-P. de Can- The organization of herbarium collections con- dolle, Bentham & Hooker, etc. that are still used sists in arranging the specimens logically to in the management of historical herbaria find and reclassify them easily in the appro- whose original classification is voluntarily pre- priate storage units. In the vascular plant col- served. lections, commonly used methods are systema- Recent classification systems based on molecu- tic classification, alphabetical classification, or lar phylogenies have developed, and herbaria combinations of both. -
Ailanthus Excelsa Roxb
Ailanthus excelsa Roxb. Simaroubaceae maharukh LOCAL NAMES Arabic (ailanthus,neem hindi); English (ailanthus,coramandel ailanto,tree- of-heaven); Gujarati (aduso,ardusi,bhutrakho); Hindi (maharuk,ardu,ardusi,arua,horanim maruk,aduso,mahanim,mahrukh,maruf,pedu,Pee vepachettu,pir nim); Nepali (maharukh); Sanskrit (madala); Tamil (periamaram,peru,perumaran,pimaram,pinari); Trade name (maharukh) BOTANIC DESCRIPTION Ailanthus excelsa is a large deciduous tree, 18-25 m tall; trunk straight, 60-80 cm in diameter; bark light grey and smooth, becoming grey-brown and rough on large trees, aromatic, slightly bitter. Leaves alternate, pinnately compound, large, 30-60 cm or more in length; leaflets 8-14 or more pairs, long stalked, ovate or broadly lance shaped from very unequal base, 6-10 cm long, 3-5 cm wide, often curved, long pointed, hairy gland; edges coarsely toothed and often lobed. Flower clusters droop at leaf bases, shorter than leaves, much branched; flowers many, mostly male and female on different trees, short stalked, greenish-yellow; calyx 5 lobed; 5 narrow petals spreading 6 mm across; stamens 10; on other flowers, 2-5 separate pistils, each with elliptical ovary, 1 ovule, and slender style. Fruit a 1-seeded samara, lance shaped, flat, pointed at ends, 5 cm long, 1 cm wide, copper red, strongly veined, twisted at the base The generic name ‘Ailanthus’ comes from ‘ailanthos’ (tree of heaven), the Indonesian name for Ailanthus moluccana. BIOLOGY The flowers appear in large open clusters among the leaves towards the end of the cold season. Male, female and bisexual flowers are intermingled on the same tree. The fruits ripen just before the onset of the monsoon. -
Plant Conservation Alliance®S Alien Plant Working Group Tree of Heaven Ailanthus Altissima (Mill.) Swingle Quassia Family (Sima
FACT SHEET: TREE OF HEAVEN Tree of Heaven Ailanthus altissima (Mill.) Swingle Quassia family (Simaroubaceae) NATIVE RANGE Central China DESCRIPTION Tree-of-heaven, also known as ailanthus, Chinese sumac, and stinking shumac, is a rapidly growing, deciduous tree in the mostly tropical quassia family (Simaroubaceae). Mature trees can reach 80 feet or more in height. Ailanthus has smooth stems with pale gray bark, and twigs which are light chestnut brown, especially in the dormant season. Its large compound leaves, 1-4 feet in length, are composed of 11-25 smaller leaflets and alternate along the stems. Each leaflet has one to several glandular teeth near the base. In late spring, clusters of small, yellow-green flowers appear near the tips of branches. Seeds are produced on female trees in late summer to early fall, in flat, twisted, papery structures called samaras, which may remain on the trees for long periods of time. The wood of ailanthus is soft, weak, coarse-grained, and creamy white to light brown in color. All parts of the tree, especially the flowers, have a strong, offensive odor, which some have likened to peanuts or cashews. NOTE: Correct identification of ailanthus is essential. Several native shrubs, like sumacs, and trees, like ash, black walnut and pecan, can be confused with ailanthus. Staghorn sumac (Rhus typhina), native to the eastern U.S., is distinguished from ailanthus by its fuzzy, reddish-brown branches and leaf stems, erect, red, fuzzy fruits, and leaflets with toothed margins. ECOLOGICAL THREAT Tree-of-heaven is a prolific seed producer, grows rapidly, and can overrun native vegetation. -
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. -
Brisbane Native Plants by Suburb
INDEX - BRISBANE SUBURBS SPECIES LIST Acacia Ridge. ...........15 Chelmer ...................14 Hamilton. .................10 Mayne. .................25 Pullenvale............... 22 Toowong ....................46 Albion .......................25 Chermside West .11 Hawthorne................. 7 McDowall. ..............6 Torwood .....................47 Alderley ....................45 Clayfield ..................14 Heathwood.... 34. Meeandah.............. 2 Queensport ............32 Trinder Park ...............32 Algester.................... 15 Coopers Plains........32 Hemmant. .................32 Merthyr .................7 Annerley ...................32 Coorparoo ................3 Hendra. .................10 Middle Park .........19 Rainworth. ..............47 Underwood. ................41 Anstead ....................17 Corinda. ..................14 Herston ....................5 Milton ...................46 Ransome. ................32 Upper Brookfield .......23 Archerfield ...............32 Highgate Hill. ........43 Mitchelton ...........45 Red Hill.................... 43 Upper Mt gravatt. .......15 Ascot. .......................36 Darra .......................33 Hill End ..................45 Moggill. .................20 Richlands ................34 Ashgrove. ................26 Deagon ....................2 Holland Park........... 3 Moorooka. ............32 River Hills................ 19 Virginia ........................31 Aspley ......................31 Doboy ......................2 Morningside. .........3 Robertson ................42 Auchenflower -
Moths of Ohio Guide
MOTHS OF OHIO field guide DIVISION OF WILDLIFE This booklet is produced by the ODNR Division of Wildlife as a free publication. This booklet is not for resale. Any unauthorized INTRODUCTION reproduction is prohibited. All images within this booklet are copyrighted by the Division of Wildlife and it’s contributing artists and photographers. For additional information, please call 1-800-WILDLIFE. Text by: David J. Horn Ph.D Moths are one of the most diverse and plentiful HOW TO USE THIS GUIDE groups of insects in Ohio, and the world. An es- Scientific Name timated 160,000 species have thus far been cata- Common Name Group and Family Description: Featured Species logued worldwide, and about 13,000 species have Secondary images 1 Primary Image been found in North America north of Mexico. Secondary images 2 Occurrence We do not yet have a clear picture of the total Size: when at rest number of moth species in Ohio, as new species Visual Index Ohio Distribution are still added annually, but the number of species Current Page Description: Habitat & Host Plant is certainly over 3,000. Although not as popular Credit & Copyright as butterflies, moths are far more numerous than their better known kin. There is at least twenty Compared to many groups of animals, our knowledge of moth distribution is very times the number of species of moths in Ohio as incomplete. Many areas of the state have not been thoroughly surveyed and in some there are butterflies. counties hardly any species have been documented. Accordingly, the distribution maps in this booklet have three levels of shading: 1. -
Samia Cynthia in New Jersey Book Review, Market- Place, Metamorphosis, Announcements, Membership Updates
________________________________________________________________________________________ Volume 61, Number 4 Winter 2019 www.lepsoc.org ________________________________________________________________________________________ Inside: Butterflies of Papua Southern Pearly Eyes in exotic Louisiana venue Philippine butterflies and moths: a new website The Lepidopterists’ Society collecting statement updated Lep Soc, Southern Lep Soc, and Assoc of Trop Lep combined meeting Butterfly vicariance in southeast Asia Samia cynthia in New Jersey Book Review, Market- place, Metamorphosis, Announcements, Membership Updates ... and more! ________________________________________________________________________________________ _________________________________________________________ Contents www.lepsoc.org ________________________________________________________ Digital Collecting -- Butterflies of Papua, Indonesia ____________________________________ Bill Berthet. .......................................................................................... 159 Volume 61, Number 4 Butterfly vicariance in Southeast Asia Winter 2019 John Grehan. ........................................................................................ 168 Metamorphosis. ....................................................................................... 171 The Lepidopterists’ Society is a non-profit ed- Membership Updates. ucational and scientific organization. The ob- Chris Grinter. ....................................................................................... 171 -
Vascular Plant Families of the United States Grouped by Diagnostic Features
Humboldt State University Digital Commons @ Humboldt State University Botanical Studies Open Educational Resources and Data 12-6-2019 Vascular Plant Families of the United States Grouped by Diagnostic Features James P. Smith Jr Humboldt State University, [email protected] Follow this and additional works at: https://digitalcommons.humboldt.edu/botany_jps Part of the Botany Commons Recommended Citation Smith, James P. Jr, "Vascular Plant Families of the United States Grouped by Diagnostic Features" (2019). Botanical Studies. 96. https://digitalcommons.humboldt.edu/botany_jps/96 This Flora of the United States and North America is brought to you for free and open access by the Open Educational Resources and Data at Digital Commons @ Humboldt State University. It has been accepted for inclusion in Botanical Studies by an authorized administrator of Digital Commons @ Humboldt State University. For more information, please contact [email protected]. FLOWERING PLANT FAMILIES OF THE UNITED STATES GROUPED BY DIAGNOSTIC FEATURES James P. Smith, Jr. Professor Emeritus of Botany Department of Biological Sciences Humboldt State University Second edition — 6 December 2019 The focus is on families of plants found in the conterminous United States, including ornamentals. The listing of a family is not meant to imply that every species has that feature. I am using a fewfamily names, such as Liliaceae, Plantaginaceae, and Scrophulariaceae, in the traditional sense, because their limits remain unsettled. Parasitic on branches Dioscoreaceae -
Plants from the Brazilian Traditional Medicine: Species from the Books Of
Revista Brasileira de Farmacognosia 27 (2017) 388–400 ww w.elsevier.com/locate/bjp Original Article Plants from the Brazilian Traditional Medicine: species from the books of the Polish physician Piotr Czerniewicz (Pedro Luiz Napoleão Chernoviz, 1812–1881) a,c d b,c b,c,∗ Letícia M. Ricardo , Juliana de Paula-Souza , Aretha Andrade , Maria G.L. Brandão a Ministério da Saúde, Departamento de Assistência Farmacêutica e Insumos Estratégicos, Esplanada dos Ministérios, Brasília, DF, Brazil b Centro Especializado em Plantas Aromáticas, Medicinais e Tóxicas, Museu de História Natural e Jardim Botânico, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil c Faculdade de Farmácia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil d Universidade Federal de São João del Rei, Campus Sete Lagoas, Sete Lagoas, MG, Brazil a b s t r a c t a r t i c l e i n f o Article history: The Brazilian flora is very rich in medicinal plants, and much information about the traditional use of Received 1 October 2016 the Brazilian plants is only available from early literature and we are facing a rapid process of loss of Accepted 10 January 2017 biodiversity. To retrieve data about useful plants registered in the books of the Polish physicist P.L.N. Available online 2 March 2017 Chernoviz, who lived in Brazil for 15 years in the 19th century. The aim is to improve our knowledge about Brazilian plants, and to ensure the benefits of sharing it with potential users. Data about Brazilian Keywords: plants were obtained from six editions of the book Formulary and Medical Guide (Formulário e Guia Historical records Médico), published in 1864, 1874, 1888, 1892, 1897 and 1920. -
APPENDIX K Biological Resource Tables
APPENDIX K Biological Resource Tables APPENDIX K Biology Addendum VASCULAR SPECIES GYMNOSPERMS AND GNETOPHYTES PINACEAE—PINE FAMILY Pinus sp.—pine MONOCOTS ARECACEAE—PALM FAMILY * Archontophoenix cunninghamiana—queen palm * Washingtonia robusta—Washington fan palm EUDICOTS APOCYNACEAE—DOGBANE FAMILY * Nerium oleander—oleander ARALIACEAE—GINSENG FAMILY * Hedera helix—English ivy HAMAMELIDACEAE—WITCH HAZEL FAMILY * Liquidambar sp.—sweet gum MYRTACEAE—MYRTLE FAMILY * Eucalyptus sp.—eucalyptus * Eucalyptus sideroxylon—red ironbark ROSACEAE—ROSE FAMILY * Eriobotrya deflexa—bronze loquat * Rhaphiolepis indica—India hawthorn SCROPHULARIACEAE—FIGWORT FAMILY * Myoporum laetum—myoporum SIMAROUBACEAE—QUASSIA OR SIMAROUBA FAMILY * Ailanthus altissima—tree of heaven ULMACEAE—ELM FAMILY * Ulmus parvifolia—Chinese elm * signifies introduced (non-native) species K-1 February 2016 APPENDIX K (Continued) BIRD Accipiter cooperii—Cooper’s hawk Bombycilla cedrorum—cedar waxwing Corvus brachyrhynchos—American crow Mimus polyglottos—northern mockingbird Spinus psaltria—lesser goldfinch Zenaida macroura—mourning dove Haemorhous mexicanus—house finch K-2 February 2016 APPENDIX K (Continued) Primary Habitat Associations/ Life Form/ Blooming Period/ Elevation Range (feet) Potential to Occur Coastal bluff scrub, coastal dunes, coastal scrub; sandy or gravelly/ annual herb/ Mar–June/ 3-1001 Not expected to occur. The site is outside of the species’ known elevation range and there is no suitable habitat present. Chaparral, coastal scrub, riparian forest, riparian scrub, riparian woodland; sandy, mesic/ perennial Not expected to occur. The site is outside of the species’ known deciduous shrub/ (Feb) May–Sep/ 49-3002 elevation range and there is no suitable habitat present. Chaparral, cismontane woodland, coastal scrub; rocky/ perennial rhizomatous herb/ Feb–June/ 591- Not expected to occur. No suitable habitat present. 3281 Coastal bluff scrub, coastal dunes, coastal scrub, valley and foothill grassland; alkaline or clay/ Not expected to occur. -
Tree Height Growth in a Neotropical Rain Forest
Ecology, 82(5), 2001, pp. 1460±1472 q 2001 by the Ecological Society of America GETTING TO THE CANOPY: TREE HEIGHT GROWTH IN A NEOTROPICAL RAIN FOREST DEBORAH A. CLARK1 AND DAVID B. CLARK1 Department of Biology, University of Missouri±St. Louis, 8001 Natural Bridge Road, St. Louis, Missouri 63121-4499, USA Abstract. There is still limited understanding of the processes underlying forest dy- namics in the world's tropical rain forests, ecosystems of disproportionate importance in terms of global biogeochemistry and biodiversity. Particularly poorly documented are the nature and time scale of upward height growth during regeneration by the tree species in these communities. In this study, we assessed long-term height growth through ontogeny for a diverse group of canopy and emergent tree species in a lowland neotropical rain forest (the La Selva Biological Station, northeastern Costa Rica). Species were evaluated based on annual height measurements of large samples of individuals in all postseedling size classes, over a 16-yr period (.11 000 increments). The study species were seven nonpi- oneers (Minquartia guianensis, Lecythis ampla, Hymenolobium mesoamericanum, Sima- rouba amara, Dipteryx panamensis, Balizia elegans, and Hyeronima alchorneoides) and two pioneers (Cecropia obtusifolia and Cecropia insignis). For each species, inherent height growth capacity was estimated as the mean of the ®ve largest annual height increments (from different individuals) in each juvenile size class (from 50 cm tall to 20 cm in diameter). All species showed marked ontogenetic increases in this measure of height growth potential. At all sizes, there were highly signi®cant differences among species in height growth potential.