Achievements in Research | 2014
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Indoor Plants Or Houseplants
Visit us on the Web: www.gardeninghelp.org Indoor Plants or Houseplants Over the past twenty years houseplants have grown in popularity. Offered in a wide variety of sizes, shapes, colors and textures, houseplants beautify our homes and help soften our environment. They have been scientifically proven to improve our health by lowering blood pressure and removing pollutants from the air we breathe. When selecting a houseplant, choose reputable suppliers who specialize in growing houseplants. Get off to a good start by thoroughly examining each plant. Watch for brown edges and spindly growth with elongated stems and large gaps between new leaves. Inspect leaves and stem junctions for signs of insect or disease problems. Check any support stakes to make sure they are not hiding broken stems or branches. Finally, make sure the plant is placed in an area that suits its optimal requirements for light, temperature and humidity. Where to Place Your House Plants With the exception of the very darkest areas, you can always find a houseplant with growth requirements to match the environmental conditions in your home. The most important factors are light intensity and duration. The best way to determine the intensity of light at a window exposure area is to measure it with a light meter. A light meter measures light in units called foot-candles. One foot-candle is the amount of light from a candle spread over a square foot of surface area. Plants that prefer low light may produce dull, lifeless-looking leaves when exposed to bright light. Bright light can also cause leaf spots or brown-tipped scorched margins. -
Hairy Braya (Braya Pilosa)
SPECIES STATUS REPORT Hairy Braya (Braya pilosa) in the Northwest Territories Threatened December 2012 Status of Hairy Braya in the NWT Species at Risk Committee status reports are working documents used in assigning the status of species suspected of being at risk in the Northwest Territories (NWT). Suggested citation: Species at Risk Committee. 2012. Species Status Report for Hairy Braya (Braya pilosa) in the Northwest Territories. Species at Risk Committee, Yellowknife, NT. © Government of the Northwest Territories on behalf of the Species at Risk Committee ISBN: 978-0-7708-0202-8 Production note: The drafts of this report were prepared by James G. Harris, prepared under contract with the Government of the Northwest Territories, and edited by Joanna Wilson and Michelle Henderson. For additional copies contact: Species at Risk Secretariat c/o SC6, Department of Environment and Natural Resources P.O. Box 1320 Yellowknife, NT X1A 2L9 Tel.: (855) 783-4301 (toll free) Fax.: (867) 873-0293 E-mail: [email protected] www.nwtspeciesatrisk.ca ABOUT THE SPECIES AT RISK COMMITTEE The Species at Risk Committee was established under the Species at Risk (NWT) Act. It is an independent committee of experts responsible for assessing the biological status of species at risk in the NWT. The Committee uses the assessments to make recommendations on the listing of species at risk. The Committee uses objective biological criteria in its assessments and does not consider socio-economic factors. Assessments are based on species status reports that include the best available Aboriginal traditional knowledge, community knowledge and scientific knowledge of the species. -
Two New Species of Hiptage (Malpighiaceae) from Yunnan, Southwest of China
A peer-reviewed open-access journal PhytoKeys 110: 81–89 (2018) Two new species of Hiptage... 81 doi: 10.3897/phytokeys.110.28673 RESEARCH ARTICLE http://phytokeys.pensoft.net Launched to accelerate biodiversity research Two new species of Hiptage (Malpighiaceae) from Yunnan, Southwest of China Bin Yang1,2, Hong-Bo Ding1,2, Jian-Wu Li1,2, Yun-Hong Tan1,2 1 Southeast Asia Biodiversity Research Institute, Chinese Academy of Sciences, Yezin, Nay Pyi Taw 05282, Myanmar 2 Centre for Integrative Conservation, Xishuangbanna Tropical Botanical Garden, Chinese Aca- demy of Sciences, Menglun, Mengla, Yunnan 666303, PR China Corresponding author: Yun-Hong Tan ([email protected]) Academic editor: Alexander Sennikov | Received 27 July 2018 | Accepted 30 September 2018 | Published 5 November 2018 Citation: Yang B, Ding H-B, Li J-W, Tan Y-H (2018) Two new species of Hiptage (Malpighiaceae) from Yunnan, Southwest of China. PhytoKeys 110: 81–89. https://doi.org/10.3897/phytokeys.110.28673 Abstract Hiptage pauciflora Y.H. Tan & Bin Yang and Hiptage ferruginea Y.H. Tan & Bin Yang, two new species of Malpighiaceae from Yunnan, South-western China are here described and illustrated. Morphologically, H. pauciflora Y.H. Tan & Bin Yang is similar to H. benghalensis (L.) Kurz and H. multiflora F.N. Wei; H. ferruginea Y.H. Tan & Bin Yang is similar to H. calcicola Sirirugsa. The major differences amongst these species are outlined and discussed. A diagnostic key to the two new species of Hiptage and their closely related species is provided. Keywords Hiptage, Malpighiaceae, samara, Yunnan, China Introduction Hiptage Gaertn. (Gaertner 1791) is one of the largest genera of Malpighiaceae with about 30 species of woody lianas and shrubs growing in forests of tropical South Asia, Indo-China Peninsula, Indonesia, Philippines and Southern China, including Hainan and Taiwan islands (Chen and Funston 2008, Ren et al. -
New Species and Combinations of Apocynaceae, Bignoniaceae, Clethraceae, and Cunoniaceae from the Neotropics
Anales del Jardín Botánico de Madrid 75 (2): e071 https://doi.org/10.3989/ajbm.2499 ISSN: 0211-1322 [email protected], http://rjb.revistas.csic.es/index.php/rjb Copyright: © 2018 CSIC. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial (by-nc) Spain 4.0 License. New species and combinations of Apocynaceae, Bignoniaceae, Clethraceae, and Cunoniaceae from the Neotropics Juan Francisco Morales 1,2,3 1 Missouri Botanical Garden 4344 Shaw Blvd. St. Louis, MO 63110, USA. 2 Bayreuth Center of Ecology and Environmental Research (BayCEER), University of Bayreuth, Universitätstrasse 30, 95447 Bayreuth, Germany. 3 Doctorado en Ciencias Naturales para el Desarrollo (DOCINADE), Universidad Estatal a Distancia, 474–2050 Montes de Oca, Costa Rica. [email protected], https://orcid.org/0000-0002-8906-8567 Abstract. Mandevilla arenicola J.F.Morales sp. nov. from Brazil, Clethra Resumen. Se describen e ilustran Mandevilla arenicola J.F.Morales secazu J.F.Morales sp. nov. from Costa Rica, and Weinmannia abstrusa sp. nov. de Brasil, Clethra secazu J.F.Morales sp. nov. de Costa Rica y J.F.Morales sp. nov. from Honduras are described and illustrated and Weinmannia abstrusa J.F.Morales sp. nov. de Honduras y se discuten their relationships with morphologically related species are discussed. sus relaciones con otras especies de morfología semejante. Se designan Lectotypes are designated for Anemopaegma tonduzianum Kraenzl., lectotipos para Anemopaegma tonduzianum Kraenzl., Bignonia Bignonia sarmentosa var. hirtella Benth. and Paragonia pyramidata var. sarmentosa var. hirtella Benth. and Paragonia pyramidata var. tomentosa tomentosa Bureau & K. Schum., as well as these last two names have Bureau & K.Schum., así como también se combinan estos dos últimos been combined. -
The Vascular Plants of Massachusetts
The Vascular Plants of Massachusetts: The Vascular Plants of Massachusetts: A County Checklist • First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Somers Bruce Sorrie and Paul Connolly, Bryan Cullina, Melissa Dow Revision • First A County Checklist Plants of Massachusetts: Vascular The A County Checklist First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Massachusetts Natural Heritage & Endangered Species Program Massachusetts Division of Fisheries and Wildlife Natural Heritage & Endangered Species Program The Natural Heritage & Endangered Species Program (NHESP), part of the Massachusetts Division of Fisheries and Wildlife, is one of the programs forming the Natural Heritage network. NHESP is responsible for the conservation and protection of hundreds of species that are not hunted, fished, trapped, or commercially harvested in the state. The Program's highest priority is protecting the 176 species of vertebrate and invertebrate animals and 259 species of native plants that are officially listed as Endangered, Threatened or of Special Concern in Massachusetts. Endangered species conservation in Massachusetts depends on you! A major source of funding for the protection of rare and endangered species comes from voluntary donations on state income tax forms. Contributions go to the Natural Heritage & Endangered Species Fund, which provides a portion of the operating budget for the Natural Heritage & Endangered Species Program. NHESP protects rare species through biological inventory, -
Evolutionary Comparisons of the Chloroplast Genome in Lauraceae and Insights Into Loss Events in the Magnoliids
GBE Evolutionary Comparisons of the Chloroplast Genome in Lauraceae and Insights into Loss Events in the Magnoliids Yu Song1,2,†,Wen-BinYu1,2,†, Yunhong Tan1,2,†, Bing Liu3,XinYao1,JianjunJin4, Michael Padmanaba1, Jun-Bo Yang4,*, and Richard T. Corlett1,2,* 1Center for Integrative Conservation, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Mengla, China 2Southeast Asia Biodiversity Research Institute, Chinese Academy of Sciences, Yezin, Nay Pyi Taw, Myanmar 3State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing, China 4Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China *Corresponding authors: E-mails: [email protected]; [email protected]. †These authors contributed equally to this work. Accepted: September 1, 2017 Data deposition: This project has been deposited at GenBank of NCBI under the accession number MF939337 to MF939351. Abstract Available plastomes of the Lauraceae show similar structure and varied size, but there has been no systematic comparison across the family. In order to understand the variation in plastome size and structure in the Lauraceae and related families of magnoliids, we here compare 47 plastomes, 15 newly sequenced, from 27 representative genera. We reveal that the two shortest plastomes are in the parasitic Lauraceae genus Cassytha, with lengths of 114,623 (C. filiformis) and 114,963 bp (C. capillaris), and that they have lost NADH dehydrogenase (ndh) genes in the large single-copy region and one entire copy of the inverted repeat (IR) region. The plastomes of the core Lauraceae group, with lengths from 150,749 bp (Nectandra angustifolia) to 152,739 bp (Actinodaphne trichocarpa), have lost trnI-CAU, rpl23, rpl2,afragmentofycf2, and their intergenic regions in IRb region, whereas the plastomes of the basal Lauraceae group, with lengths from 157,577 bp (Eusideroxylon zwageri) to 158,530 bp (Beilschmiedia tungfangen- sis), have lost rpl2 in IRa region. -
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 -
Native Plants for Your Backyard
U.S. Fish & Wildlife Service Native Plants for Your Backyard Native plants of the Southeastern United States are more diverse in number and kind than in most other countries, prized for their beauty worldwide. Our native plants are an integral part of a healthy ecosystem, providing the energy that sustains our forests and wildlife, including important pollinators and migratory birds. By “growing native” you can help support native wildlife. This helps sustain the natural connections that have developed between plants and animals over thousands of years. Consider turning your lawn into a native garden. You’ll help the local environment and often use less water and spend less time and money maintaining your yard if the plants are properly planted. The plants listed are appealing to many species of wildlife and will look attractive in your yard. To maximize your success with these plants, match the right plants with the right site conditions (soil, pH, sun, and moisture). Check out the resources on the back of this factsheet for assistance or contact your local extension office for soil testing and more information about these plants. Shrubs Trees Vines Wildflowers Grasses American beautyberry Serviceberry Trumpet creeper Bee balm Big bluestem Callicarpa americana Amelanchier arborea Campsis radicans Monarda didyma Andropogon gerardii Sweetshrub Redbud Carolina jasmine Fire pink Little bluestem Calycanthus floridus Cercis canadensis Gelsemium sempervirens Silene virginica Schizachyrium scoparium Blueberry Red buckeye Crossvine Cardinal flower -
Fossil Mosses: What Do They Tell Us About Moss Evolution?
Bry. Div. Evo. 043 (1): 072–097 ISSN 2381-9677 (print edition) DIVERSITY & https://www.mapress.com/j/bde BRYOPHYTEEVOLUTION Copyright © 2021 Magnolia Press Article ISSN 2381-9685 (online edition) https://doi.org/10.11646/bde.43.1.7 Fossil mosses: What do they tell us about moss evolution? MicHAEL S. IGNATOV1,2 & ELENA V. MASLOVA3 1 Tsitsin Main Botanical Garden of the Russian Academy of Sciences, Moscow, Russia 2 Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia 3 Belgorod State University, Pobedy Square, 85, Belgorod, 308015 Russia �[email protected], https://orcid.org/0000-0003-1520-042X * author for correspondence: �[email protected], https://orcid.org/0000-0001-6096-6315 Abstract The moss fossil records from the Paleozoic age to the Eocene epoch are reviewed and their putative relationships to extant moss groups discussed. The incomplete preservation and lack of key characters that could define the position of an ancient moss in modern classification remain the problem. Carboniferous records are still impossible to refer to any of the modern moss taxa. Numerous Permian protosphagnalean mosses possess traits that are absent in any extant group and they are therefore treated here as an extinct lineage, whose descendants, if any remain, cannot be recognized among contemporary taxa. Non-protosphagnalean Permian mosses were also fairly diverse, representing morphotypes comparable with Dicranidae and acrocarpous Bryidae, although unequivocal representatives of these subclasses are known only since Cretaceous and Jurassic. Even though Sphagnales is one of two oldest lineages separated from the main trunk of moss phylogenetic tree, it appears in fossil state regularly only since Late Cretaceous, ca. -
Temporal and Spatial Origin of Gesneriaceae in the New World Inferred from Plastid DNA Sequences
bs_bs_banner Botanical Journal of the Linnean Society, 2013, 171, 61–79. With 3 figures Temporal and spatial origin of Gesneriaceae in the New World inferred from plastid DNA sequences MATHIEU PERRET1*, ALAIN CHAUTEMS1, ANDRÉA ONOFRE DE ARAUJO2 and NICOLAS SALAMIN3,4 1Conservatoire et Jardin botaniques de la Ville de Genève, Ch. de l’Impératrice 1, CH-1292 Chambésy, Switzerland 2Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Rua Santa Adélia, 166, Bairro Bangu, Santo André, Brazil 3Department of Ecology and Evolution, University of Lausanne, CH-1015 Lausanne, Switzerland 4Swiss Institute of Bioinformatics, Quartier Sorge, CH-1015 Lausanne, Switzerland Received 15 December 2011; revised 3 July 2012; accepted for publication 18 August 2012 Gesneriaceae are represented in the New World (NW) by a major clade (c. 1000 species) currently recognized as subfamily Gesnerioideae. Radiation of this group occurred in all biomes of tropical America and was accompanied by extensive phenotypic and ecological diversification. Here we performed phylogenetic analyses using DNA sequences from three plastid loci to reconstruct the evolutionary history of Gesnerioideae and to investigate its relationship with other lineages of Gesneriaceae and Lamiales. Our molecular data confirm the inclusion of the South Pacific Coronanthereae and the Old World (OW) monotypic genus Titanotrichum in Gesnerioideae and the sister-group relationship of this subfamily to the rest of the OW Gesneriaceae. Calceolariaceae and the NW genera Peltanthera and Sanango appeared successively sister to Gesneriaceae, whereas Cubitanthus, which has been previously assigned to Gesneriaceae, is shown to be related to Linderniaceae. Based on molecular dating and biogeographical reconstruction analyses, we suggest that ancestors of Gesneriaceae originated in South America during the Late Cretaceous. -
Plant Life MagillS Encyclopedia of Science
MAGILLS ENCYCLOPEDIA OF SCIENCE PLANT LIFE MAGILLS ENCYCLOPEDIA OF SCIENCE PLANT LIFE Volume 4 Sustainable Forestry–Zygomycetes Indexes Editor Bryan D. Ness, Ph.D. Pacific Union College, Department of Biology Project Editor Christina J. Moose Salem Press, Inc. Pasadena, California Hackensack, New Jersey Editor in Chief: Dawn P. Dawson Managing Editor: Christina J. Moose Photograph Editor: Philip Bader Manuscript Editor: Elizabeth Ferry Slocum Production Editor: Joyce I. Buchea Assistant Editor: Andrea E. Miller Page Design and Graphics: James Hutson Research Supervisor: Jeffry Jensen Layout: William Zimmerman Acquisitions Editor: Mark Rehn Illustrator: Kimberly L. Dawson Kurnizki Copyright © 2003, by Salem Press, Inc. All rights in this book are reserved. No part of this work may be used or reproduced in any manner what- soever or transmitted in any form or by any means, electronic or mechanical, including photocopy,recording, or any information storage and retrieval system, without written permission from the copyright owner except in the case of brief quotations embodied in critical articles and reviews. For information address the publisher, Salem Press, Inc., P.O. Box 50062, Pasadena, California 91115. Some of the updated and revised essays in this work originally appeared in Magill’s Survey of Science: Life Science (1991), Magill’s Survey of Science: Life Science, Supplement (1998), Natural Resources (1998), Encyclopedia of Genetics (1999), Encyclopedia of Environmental Issues (2000), World Geography (2001), and Earth Science (2001). ∞ The paper used in these volumes conforms to the American National Standard for Permanence of Paper for Printed Library Materials, Z39.48-1992 (R1997). Library of Congress Cataloging-in-Publication Data Magill’s encyclopedia of science : plant life / edited by Bryan D. -
Doctorat De L'université De Toulouse
En vue de l’obt ention du DOCTORAT DE L’UNIVERSITÉ DE TOULOUSE Délivré par : Université Toulouse 3 Paul Sabatier (UT3 Paul Sabatier) Discipline ou spécialité : Ecologie, Biodiversité et Evolution Présentée et soutenue par : Joeri STRIJK le : 12 / 02 / 2010 Titre : Species diversification and differentiation in the Madagascar and Indian Ocean Islands Biodiversity Hotspot JURY Jérôme CHAVE, Directeur de Recherches CNRS Toulouse Emmanuel DOUZERY, Professeur à l'Université de Montpellier II Porter LOWRY II, Curator Missouri Botanical Garden Frédéric MEDAIL, Professeur à l'Université Paul Cezanne Aix-Marseille Christophe THEBAUD, Professeur à l'Université Paul Sabatier Ecole doctorale : Sciences Ecologiques, Vétérinaires, Agronomiques et Bioingénieries (SEVAB) Unité de recherche : UMR 5174 CNRS-UPS Evolution & Diversité Biologique Directeur(s) de Thèse : Christophe THEBAUD Rapporteurs : Emmanuel DOUZERY, Professeur à l'Université de Montpellier II Porter LOWRY II, Curator Missouri Botanical Garden Contents. CONTENTS CHAPTER 1. General Introduction 2 PART I: ASTERACEAE CHAPTER 2. Multiple evolutionary radiations and phenotypic convergence in polyphyletic Indian Ocean Daisy Trees (Psiadia, Asteraceae) (in preparation for BMC Evolutionary Biology) 14 CHAPTER 3. Taxonomic rearrangements within Indian Ocean Daisy Trees (Psiadia, Asteraceae) and the resurrection of Frappieria (in preparation for Taxon) 34 PART II: MYRSINACEAE CHAPTER 4. Phylogenetics of the Mascarene endemic genus Badula relative to its Madagascan ally Oncostemum (Myrsinaceae) (accepted in Botanical Journal of the Linnean Society) 43 CHAPTER 5. Timing and tempo of evolutionary diversification in Myrsinaceae: Badula and Oncostemum in the Indian Ocean Island Biodiversity Hotspot (in preparation for BMC Evolutionary Biology) 54 PART III: MONIMIACEAE CHAPTER 6. Biogeography of the Monimiaceae (Laurales): a role for East Gondwana and long distance dispersal, but not West Gondwana (accepted in Journal of Biogeography) 72 CHAPTER 7 General Discussion 86 REFERENCES 91 i Contents.