Botanischer Garten Der Universität Tübingen

Total Page:16

File Type:pdf, Size:1020Kb

Botanischer Garten Der Universität Tübingen Botanischer Garten der Universität Tübingen 1974 – 2008 2 System FRANZ OBERWINKLER Emeritus für Spezielle Botanik und Mykologie Ehemaliger Direktor des Botanischen Gartens 2016 2016 zur Erinnerung an LEONHART FUCHS (1501-1566), 450. Todesjahr 40 Jahre Alpenpflanzen-Lehrpfad am Iseler, Oberjoch, ab 1976 20 Jahre Förderkreis Botanischer Garten der Universität Tübingen, ab 1996 für alle, die im Garten gearbeitet und nachgedacht haben 2 Inhalt Vorwort ...................................................................................................................................... 8 Baupläne und Funktionen der Blüten ......................................................................................... 9 Hierarchie der Taxa .................................................................................................................. 13 Systeme der Bedecktsamer, Magnoliophytina ......................................................................... 15 Das System von ANTOINE-LAURENT DE JUSSIEU ................................................................. 16 Das System von AUGUST EICHLER ....................................................................................... 17 Das System von ADOLF ENGLER .......................................................................................... 19 Das System von ARMEN TAKHTAJAN ................................................................................... 21 Das System nach molekularen Phylogenien ........................................................................ 22 Basale Gruppen ........................................................................................................................ 26 Amborellales ........................................................................................................................ 26 Nymphaeales, Seerosenartige Gewächse ............................................................................. 26 Austrobaileyales ................................................................................................................... 28 Schisandraceae, Spaltstaubblattgewächse ........................................................................ 28 Ceratophyllales, Hornblattartige Gewächse ......................................................................... 28 Einkeimblättrige Blütenpflanzen .............................................................................................. 29 Acorales, Kalmusartige Gewächse ....................................................................................... 30 Arales, Aronstabartige Gewächse ........................................................................................ 30 Araceae, Aronstabgewächse ............................................................................................. 30 Orontiaceae, Goldkeulengewächse .................................................................................. 31 Lemnaceae, Wasserlinsengewächse ................................................................................. 31 Alismatales, Froschlöffelartige Gewächse ........................................................................... 32 Hydrocharitaceae, Froschbißgewächse ............................................................................ 32 Butomaceae, Schwanenblumengewächse ........................................................................ 33 Alismataceae, Froschlöffelgewächse ............................................................................... 33 Juncaginaceae, Dreizackgewächse ................................................................................... 33 Potamogetonaceae, Laichkrautgewächse ......................................................................... 34 Scheuchzeriaceae, Blumenbinsengewächse ..................................................................... 34 Tofieldiaceae, Liliensimsengewächse .............................................................................. 35 Dioscoreales, Yamswurzelartige Gewächse ........................................................................ 35 Nartheciaceae, Beinbrechgewächse ................................................................................. 36 Dioscoreaceae, Yamswurzelgewächse ............................................................................. 36 Liliales, Lilienartige Gewächse ............................................................................................ 37 Melanthiaceae, Schwarzblütengewächse ......................................................................... 37 Colchicaceae, Zeitlosengewächse .................................................................................... 38 Alstroemeriaceae, Inkaliliengewächse ............................................................................. 38 Smilacaceae, Stechwindengewächse ................................................................................ 38 Liliaceae, Liliengewächse ................................................................................................ 39 Asparagales, Spargelartige Gewächse .................................................................................. 40 Iridaceae, Irisgewächse .................................................................................................... 40 Asphodelaceae, Affodillgewächse ................................................................................... 41 Hemerocallidaceae, Tagliliengewächse ........................................................................... 41 Agapanthaceae, Schmuckliliengewächse ......................................................................... 41 Alliaceae, Lauchgewächse ............................................................................................... 42 Amaryllidaceae, Narzissengewächse ............................................................................... 42 Aphyllanthaceae, Blattlosblütengewächse ....................................................................... 43 Hyacinthaceae, Hyazinthengewächse .............................................................................. 43 Anthericaceae, Grasliliengewächse .................................................................................. 44 3 Asparagaceae, Spargelgewächse ...................................................................................... 44 Ruscaceae, Mäusedorngewächse ..................................................................................... 45 Orchidales, Orchideen .......................................................................................................... 45 Commelinidae, Tradescantienartige Verwandtschaft .............................................................. 47 Typhales, Rohrkolbenartige Gewächse ................................................................................ 48 Typhaceae, Rohrkolbengewächse .................................................................................... 48 Sparganiaceae, Igelkolbengewächse ................................................................................ 48 Juncales, Binsenartige Gewächse ......................................................................................... 49 Juncaceae, Binsengewächse ............................................................................................. 49 Cyperaceae, Sauergräser .................................................................................................. 50 Poales, Süßgräser ................................................................................................................. 53 Commelinales, Tradescantienartige Gewächse .................................................................... 55 Zingiberales, Ingwerartige Gewächse .................................................................................. 56 Cannaceae, Blumenrohrgewächse .................................................................................... 56 Zweikeimblättrige Blütenpflanzen, .......................................................................................... 57 Magnoliidae, Magnolienartige Verwandtschaft ....................................................................... 58 Magnoliales, Magnolienartige Gewächse ............................................................................ 59 Laurales, Lorbeerbaumartige Gewächse .............................................................................. 60 Lauraceae, Lorbeergewächse ........................................................................................... 60 Calycanthaceae, Gewürzstrauchgewächse ....................................................................... 61 Aristolochiales, Osterluzeiartige Gewächse ......................................................................... 61 Piperales, Pfefferartige Gewächse ........................................................................................ 62 Saururaceae, Molchschwanzgewächse ............................................................................. 62 Ranunculales, Hahnenfußartige Gewächse .......................................................................... 63 Berberidaceae, Berberitzengewächse ............................................................................... 63 Nandinaceae ..................................................................................................................... 64 Ranunculaceae, Hahnenfußgewächse .............................................................................. 64 Papaveraceae, Mohngewächse ........................................................................................
Recommended publications
  • Asparagus Densiflorus SCORE: 15.0 RATING: High Risk (Kunth) Jessop
    TAXON: Asparagus densiflorus SCORE: 15.0 RATING: High Risk (Kunth) Jessop Taxon: Asparagus densiflorus (Kunth) Jessop Family: Asparagaceae Common Name(s): asparagus fern Synonym(s): Asparagopsis densiflora Kunth foxtail fern Asparagus myriocladus Baker plume asparagus Protasparagus densiflorus (Kunth) Oberm. regal fern Sprenger's asparagus fern Assessor: Chuck Chimera Status: Assessor Approved End Date: 16 Feb 2021 WRA Score: 15.0 Designation: H(HPWRA) Rating: High Risk Keywords: Tuberous Geophyte, Naturalized, Environmental Weed, Dense Cover, Bird-Dispersed Qsn # Question Answer Option Answer 101 Is the species highly domesticated? y=-3, n=0 n 102 Has the species become naturalized where grown? 103 Does the species have weedy races? Species suited to tropical or subtropical climate(s) - If 201 island is primarily wet habitat, then substitute "wet (0-low; 1-intermediate; 2-high) (See Appendix 2) High tropical" for "tropical or subtropical" 202 Quality of climate match data (0-low; 1-intermediate; 2-high) (See Appendix 2) High 203 Broad climate suitability (environmental versatility) y=1, n=0 n Native or naturalized in regions with tropical or 204 y=1, n=0 y subtropical climates Does the species have a history of repeated introductions 205 y=-2, ?=-1, n=0 y outside its natural range? 301 Naturalized beyond native range y = 1*multiplier (see Appendix 2), n= question 205 y 302 Garden/amenity/disturbance weed n=0, y = 1*multiplier (see Appendix 2) n 303 Agricultural/forestry/horticultural weed n=0, y = 2*multiplier (see Appendix 2) n 304
    [Show full text]
  • BEGONIACEAE 1. BEGONIA Linnaeus, Sp. Pl. 2: 1056. 1753
    BEGONIACEAE 秋海棠科 qiu hai tang ke Gu Cuizhi (谷粹芝 Ku Tsue-chih)1, Ching-I Peng (彭镜毅)2, Nicholas J. Turland3 Perennial succulent herbs, very rarely subshrubs. Stem erect, frequently rhizomatous, or plants tuberous and either acaulescent or shortly stemmed, rarely lianoid or climbing with adventitious roots, or stoloniferous. Leaves simple, rarely palmately compound, alternate or all basal, petiolate, stipules usually deciduous; blade often oblique and asymmetric, rarely symmetric, margin irregularly serrate and divided, occasionally entire, venation usually palmate. Flowers unisexual, plants monoecious, rarely dioecious, (1 or)2–4 to several, rarely numerous in dichotomous cyme, sometimes in panicles, with pedicel and bracts. Staminate flower: tepals 2 or 4 and decussate, usually outer ones larger, inner ones smaller; stamens usually numerous; filaments free or connate at base; anthers 2- celled, apical or lateral. Pistillate flower: tepals 2–5(–10), usually free, rarely connate at base; ovary nodding, pendulous, or ascending, 1–3-, rarely 4–8-loculed; placentae axile or parietal; styles 2 or 3(or more), free or fused at base, forked once or more; stigma turgid, spirally twisted-tortuous or U-shaped, capitate or reniform and setose-papillose. Capsule dry, sometimes berrylike, unequally or subequally 3-winged, rarely wingless and 3- or 4-horned; seeds very numerous, minute, oblong, testa pale brown, reticulate. Two or three genera and more than 1400 species: widely distributed in the tropical and subtropical regions of the world; one genus and 173 species (141 endemic) in China. Ku Tsuechih. 1999. Begoniaceae. In: Ku Tsuechih, ed., Fl. Reipubl. Popularis Sin. 52(1): 126–269. 1.
    [Show full text]
  • Proceedings Amurga Co
    PROCEEDINGS OF THE AMURGA INTERNATIONAL CONFERENCES ON ISLAND BIODIVERSITY 2011 PROCEEDINGS OF THE AMURGA INTERNATIONAL CONFERENCES ON ISLAND BIODIVERSITY 2011 Coordination: Juli Caujapé-Castells Funded and edited by: Fundación Canaria Amurga Maspalomas Colaboration: Faro Media Cover design & layout: Estudio Creativo Javier Ojeda © Fundación Canaria Amurga Maspalomas Gran Canaria, December 2013 ISBN: 978-84-616-7394-0 How to cite this volume: Caujapé-Castells J, Nieto Feliner G, Fernández Palacios JM (eds.) (2013) Proceedings of the Amurga international conferences on island biodiversity 2011. Fundación Canaria Amurga-Maspalomas, Las Palmas de Gran Canaria, Spain. All rights reserved. Any unauthorized reprint or use of this material is prohibited. No part of this book may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system without express written permission from the author / publisher. SCIENTIFIC EDITORS Juli Caujapé-Castells Jardín Botánico Canario “Viera y Clavijo” - Unidad Asociada CSIC Consejería de Medio Ambiente y Emergencias, Cabildo de Gran Canaria Gonzalo Nieto Feliner Real Jardín Botánico de Madrid-CSIC José María Fernández Palacios Universidad de La Laguna SCIENTIFIC COMMITTEE Juli Caujapé-Castells, Gonzalo Nieto Feliner, David Bramwell, Águedo Marrero Rodríguez, Julia Pérez de Paz, Bernardo Navarro-Valdivielso, Ruth Jaén-Molina, Rosa Febles Hernández, Pablo Vargas. Isabel Sanmartín. ORGANIZING COMMITTEE Pedro
    [Show full text]
  • 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
    [Show full text]
  • Redmond Watershed Preserve King County, Washington
    Vascular Plant List: Redmond Watershed Preserve King County, Washington Partial list covers plants found in the 800-acre watershed managed by the city of Redmond primarily as a nature preserve. Habitats include shady 90-year old forest, sunny disturbed utility corridors, ephemeral drainages, perennial streams, ponds and other wetlands. The preserve has 7 miles of trails (see external links below), most of which are multi-use and a couple of which are ADA accessible. List originally compiled by Fred Weinmann in February 2002. Ron Bockelman made additions in 2018. 128 species (83 native, 45 introduced) Directions: 21760 NE Novelty Hill Rd, Redmond, WA 98052 is the physical address. Drive 2.3 miles east on Novelty Hill Rd from its junction with Avondale Rd. Turn left at the entrance across from 218 Ave NE and continue to the parking lot, information kiosk, and restrooms. Ownership: City of Redmond Access: Open during daylight hours. No pets allowed. Permits: None External Links: https://www.wta.org/go-hiking/hikes/redmond-watershed-preserve https://www.alltrails.com/parks/us/washington/redmond-watershed-preserve Coordinates: 47.695943°, -122.051161° Elevation: 300 - 700 feet Key to symbols: * = Introduced species. ? = Uncertain identification. + = Species is represented by two or more subspecies or varieties in Washington; the species in this list has not been identified to subspecies or variety. ! = Species is not known to occur near this location based on specimen records in the PNW Herbaria database, and may be misidentified. # = Species name could not be resolved to an accepted name; the name may be misspelled. Numeric superscripts after a scientific name indicates the name was more broadly circumscribed in the past, and has since been split into two or more accepted taxa in Washington.
    [Show full text]
  • Introduction to Common Native & Invasive Freshwater Plants in Alaska
    Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska Cover photographs by (top to bottom, left to right): Tara Chestnut/Hannah E. Anderson, Jamie Fenneman, Vanessa Morgan, Dana Visalli, Jamie Fenneman, Lynda K. Moore and Denny Lassuy. Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska This document is based on An Aquatic Plant Identification Manual for Washington’s Freshwater Plants, which was modified with permission from the Washington State Department of Ecology, by the Center for Lakes and Reservoirs at Portland State University for Alaska Department of Fish and Game US Fish & Wildlife Service - Coastal Program US Fish & Wildlife Service - Aquatic Invasive Species Program December 2009 TABLE OF CONTENTS TABLE OF CONTENTS Acknowledgments ............................................................................ x Introduction Overview ............................................................................. xvi How to Use This Manual .................................................... xvi Categories of Special Interest Imperiled, Rare and Uncommon Aquatic Species ..................... xx Indigenous Peoples Use of Aquatic Plants .............................. xxi Invasive Aquatic Plants Impacts ................................................................................. xxi Vectors ................................................................................. xxii Prevention Tips .................................................... xxii Early Detection and Reporting
    [Show full text]
  • Phenolic Compounds and Antimicrobial Properties of Begonia Grandis Dryand
    Botanica Pacifica. A journal of plant science and conservation. 2019. 8(2): 51–61 DOI: 10.17581/bp.2019.08202 Phenolic compounds and antimicrobial properties of Begonia grandis Dryand. subsp. grandis leaves Evgeniya A. Karpova1*, Alexander A. Krasnikov1, Tatyana D. Fershalova1, Elena V. Baikova1, Anastasia A. Petruk1 & Yulia L. Yakimova2 Evgeniya A. Karpova1* ABSTRACT e-mail: [email protected] We studied the leaves of Begonia grandis Dryand. subsp. grandis, the northern- Alexander A. Krasnikov1 most and most cold-resistant representative of the predominantly tropical genus e-mail: [email protected] Begonia, by histochemical methods. In glandular and nonglandular trichomes as Tatyana D. Fershalova1 well as in the epidermal cells of B. grandis Dryand. subsp. grandis leaves, phenolic e-mail: [email protected] compounds, including flavonoids, as well as terpenoids and carbonyl compounds were detected. The patterns of phenolic compounds in the acetone and ethanol Elena V. Baikova1 leaf exudates and in leaves as a whole were similar and contained oxalic, citric, e-mail: [email protected] and gallic acids, isoquercitrin, and orientin. Concentrations of phenolic com- Anastasia A. Petruk1 pounds in the acetone and ethanol exudates constituted 0.10 % and 2.59 % of e-mail: [email protected] all phenolic compounds in the leaves, respectively. Antimicrobial effects of the aqueous ethanol extract and of the ethanol exudate against reference strains of Yulia L. Yakimova2 Bacillus subtilis, Staphylococcus aureus, and Candida albicans were detected at the disc e-mail: [email protected] con tents of 50.0 and 45.8 μg, respectively. The observed set of characteristics can be used in a targeted search for highly antimicrobial species of Begoniaceaе.
    [Show full text]
  • Complete Chloroplast Genomes Shed Light on Phylogenetic
    www.nature.com/scientificreports OPEN Complete chloroplast genomes shed light on phylogenetic relationships, divergence time, and biogeography of Allioideae (Amaryllidaceae) Ju Namgung1,4, Hoang Dang Khoa Do1,2,4, Changkyun Kim1, Hyeok Jae Choi3 & Joo‑Hwan Kim1* Allioideae includes economically important bulb crops such as garlic, onion, leeks, and some ornamental plants in Amaryllidaceae. Here, we reported the complete chloroplast genome (cpDNA) sequences of 17 species of Allioideae, fve of Amaryllidoideae, and one of Agapanthoideae. These cpDNA sequences represent 80 protein‑coding, 30 tRNA, and four rRNA genes, and range from 151,808 to 159,998 bp in length. Loss and pseudogenization of multiple genes (i.e., rps2, infA, and rpl22) appear to have occurred multiple times during the evolution of Alloideae. Additionally, eight mutation hotspots, including rps15-ycf1, rps16-trnQ-UUG, petG-trnW-CCA , psbA upstream, rpl32- trnL-UAG , ycf1, rpl22, matK, and ndhF, were identifed in the studied Allium species. Additionally, we present the frst phylogenomic analysis among the four tribes of Allioideae based on 74 cpDNA coding regions of 21 species of Allioideae, fve species of Amaryllidoideae, one species of Agapanthoideae, and fve species representing selected members of Asparagales. Our molecular phylogenomic results strongly support the monophyly of Allioideae, which is sister to Amaryllioideae. Within Allioideae, Tulbaghieae was sister to Gilliesieae‑Leucocoryneae whereas Allieae was sister to the clade of Tulbaghieae‑ Gilliesieae‑Leucocoryneae. Molecular dating analyses revealed the crown age of Allioideae in the Eocene (40.1 mya) followed by diferentiation of Allieae in the early Miocene (21.3 mya). The split of Gilliesieae from Leucocoryneae was estimated at 16.5 mya.
    [Show full text]
  • Adlumia Fungosa (Aiton) Greene Ex Britton
    Adlumia fungosa (Aiton) Greene ex Britton Common Names: Allegheny vine, Climbing Fumitory, Mountain-fringe (1, 3) Etymology: Adlumia for John Adlum, amateur botanist of the late 18th century and early 19th century; fungosa: from the Greek ‘fung’, meaning spongy or mushroom-like (5, 7). Botanical synonyms: Fumaria fungosa (Aiton), Bicuculla fungosa (Aiton) Kuntze, Adlumia cirrhosa (Raf.), Fumaria recta (Michx.), Bicuculla fungosa (Aiton), Bicuculla fumarioides (Borkh.), Corydalis fungosa (Aiton) (3, 11, 14). FAMILY: Papaveraceae (the poppy family) Quick Notable Features: ¬ Spongy, tube-like flowers, each individual flower lasting all summer ¬ Prehensile, climbing leaves ¬ Short, often un-noticeable petiole Plant Height: A. fungosa can climb to 4m, but averages 3m (4, 8). Subspecies/varieties: none found (3) Most Likely Confused with: Rosa setigera and Rubus laciniatus, as well as other Fumarioideae species, some trifoliate Fabaceae (most notably Amphicarpaea bracteata and Lespedeza procumbens), and Ranunculaceae climbers like Clematis virginiana and C. occidentalis. Habitat Preference: A. fungosa prefers full sun, although it can tolerate shade. It is often found in moist or freshly burned woods, as well on rocky slopes and slightly acidic soils. It prefers sites protected from wind (8, 12). It was reported in 1999 in Great Smoky Mountains National Park growing on Betula lenta along streams at 2670m elevation (21). Geographic Distribution in Michigan: Allegheny-vine is found sporadically in Michigan 1 (in a geographic sense; habitat analysis may provide some explanation as to why). It is found in the following counties: Berrien, Charlevoix, Chippewa, Delta, Hillsdale, Ingham, Ishpeming, Kent, Luce, Mackinack, Menominee, Muskegon, Ottawa, Presque Isle, St. Clair, Van Buren, Washtenaw, and Wayne (2).
    [Show full text]
  • Devonian Plant Fossils a Window Into the Past
    EPPC 2018 Sponsors Academic Partners PROGRAM & ABSTRACTS ACKNOWLEDGMENTS Scientific Committee: Zhe-kun Zhou Angelica Feurdean Jenny McElwain, Chair Tao Su Walter Finsinger Fraser Mitchell Lutz Kunzmann Graciela Gil Romera Paddy Orr Lisa Boucher Lyudmila Shumilovskikh Geoffrey Clayton Elizabeth Wheeler Walter Finsinger Matthew Parkes Evelyn Kustatscher Eniko Magyari Colin Kelleher Niall W. Paterson Konstantinos Panagiotopoulos Benjamin Bomfleur Benjamin Dietre Convenors: Matthew Pound Fabienne Marret-Davies Marco Vecoli Ulrich Salzmann Havandanda Ombashi Charles Wellman Wolfram M. Kürschner Jiri Kvacek Reed Wicander Heather Pardoe Ruth Stockey Hartmut Jäger Christopher Cleal Dieter Uhl Ellen Stolle Jiri Kvacek Maria Barbacka José Bienvenido Diez Ferrer Borja Cascales-Miñana Hans Kerp Friðgeir Grímsson José B. Diez Patricia Ryberg Christa-Charlotte Hofmann Xin Wang Dimitrios Velitzelos Reinhard Zetter Charilaos Yiotis Peta Hayes Jean Nicolas Haas Joseph D. White Fraser Mitchell Benjamin Dietre Jennifer C. McElwain Jenny McElwain Marie-José Gaillard Paul Kenrick Furong Li Christine Strullu-Derrien Graphic and Website Design: Ralph Fyfe Chris Berry Peter Lang Irina Delusina Margaret E. Collinson Tiiu Koff Andrew C. Scott Linnean Society Award Selection Panel: Elena Severova Barry Lomax Wuu Kuang Soh Carla J. Harper Phillip Jardine Eamon haughey Michael Krings Daniela Festi Amanda Porter Gar Rothwell Keith Bennett Kamila Kwasniewska Cindy V. Looy William Fletcher Claire M. Belcher Alistair Seddon Conference Organization: Jonathan P. Wilson
    [Show full text]
  • National List of Vascular Plant Species That Occur in Wetlands 1996
    National List of Vascular Plant Species that Occur in Wetlands: 1996 National Summary Indicator by Region and Subregion Scientific Name/ North North Central South Inter- National Subregion Northeast Southeast Central Plains Plains Plains Southwest mountain Northwest California Alaska Caribbean Hawaii Indicator Range Abies amabilis (Dougl. ex Loud.) Dougl. ex Forbes FACU FACU UPL UPL,FACU Abies balsamea (L.) P. Mill. FAC FACW FAC,FACW Abies concolor (Gord. & Glend.) Lindl. ex Hildebr. NI NI NI NI NI UPL UPL Abies fraseri (Pursh) Poir. FACU FACU FACU Abies grandis (Dougl. ex D. Don) Lindl. FACU-* NI FACU-* Abies lasiocarpa (Hook.) Nutt. NI NI FACU+ FACU- FACU FAC UPL UPL,FAC Abies magnifica A. Murr. NI UPL NI FACU UPL,FACU Abildgaardia ovata (Burm. f.) Kral FACW+ FAC+ FAC+,FACW+ Abutilon theophrasti Medik. UPL FACU- FACU- UPL UPL UPL UPL UPL NI NI UPL,FACU- Acacia choriophylla Benth. FAC* FAC* Acacia farnesiana (L.) Willd. FACU NI NI* NI NI FACU Acacia greggii Gray UPL UPL FACU FACU UPL,FACU Acacia macracantha Humb. & Bonpl. ex Willd. NI FAC FAC Acacia minuta ssp. minuta (M.E. Jones) Beauchamp FACU FACU Acaena exigua Gray OBL OBL Acalypha bisetosa Bertol. ex Spreng. FACW FACW Acalypha virginica L. FACU- FACU- FAC- FACU- FACU- FACU* FACU-,FAC- Acalypha virginica var. rhomboidea (Raf.) Cooperrider FACU- FAC- FACU FACU- FACU- FACU* FACU-,FAC- Acanthocereus tetragonus (L.) Humm. FAC* NI NI FAC* Acanthomintha ilicifolia (Gray) Gray FAC* FAC* Acanthus ebracteatus Vahl OBL OBL Acer circinatum Pursh FAC- FAC NI FAC-,FAC Acer glabrum Torr. FAC FAC FAC FACU FACU* FAC FACU FACU*,FAC Acer grandidentatum Nutt.
    [Show full text]
  • Global Survey of Ex Situ Betulaceae Collections Global Survey of Ex Situ Betulaceae Collections
    Global Survey of Ex situ Betulaceae Collections Global Survey of Ex situ Betulaceae Collections By Emily Beech, Kirsty Shaw and Meirion Jones June 2015 Recommended citation: Beech, E., Shaw, K., & Jones, M. 2015. Global Survey of Ex situ Betulaceae Collections. BGCI. Acknowledgements BGCI gratefully acknowledges the many botanic gardens around the world that have contributed data to this survey (a full list of contributing gardens is provided in Annex 2). BGCI would also like to acknowledge the assistance of the following organisations in the promotion of the survey and the collection of data, including the Royal Botanic Gardens Edinburgh, Yorkshire Arboretum, University of Liverpool Ness Botanic Gardens, and Stone Lane Gardens & Arboretum (U.K.), and the Morton Arboretum (U.S.A). We would also like to thank contributors to The Red List of Betulaceae, which was a precursor to this ex situ survey. BOTANIC GARDENS CONSERVATION INTERNATIONAL (BGCI) BGCI is a membership organization linking botanic gardens is over 100 countries in a shared commitment to biodiversity conservation, sustainable use and environmental education. BGCI aims to mobilize botanic gardens and work with partners to secure plant diversity for the well-being of people and the planet. BGCI provides the Secretariat for the IUCN/SSC Global Tree Specialist Group. www.bgci.org FAUNA & FLORA INTERNATIONAL (FFI) FFI, founded in 1903 and the world’s oldest international conservation organization, acts to conserve threatened species and ecosystems worldwide, choosing solutions that are sustainable, based on sound science and take account of human needs. www.fauna-flora.org GLOBAL TREES CAMPAIGN (GTC) GTC is undertaken through a partnership between BGCI and FFI, working with a wide range of other organisations around the world, to save the world’s most threated trees and the habitats which they grow through the provision of information, delivery of conservation action and support for sustainable use.
    [Show full text]