Neonotonia Wightii Scientific Name Neonotonia Wightii (Wight & Arn.) J.A
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Fruits and Seeds of Genera in the Subfamily Faboideae (Fabaceae)
Fruits and Seeds of United States Department of Genera in the Subfamily Agriculture Agricultural Faboideae (Fabaceae) Research Service Technical Bulletin Number 1890 Volume I December 2003 United States Department of Agriculture Fruits and Seeds of Agricultural Research Genera in the Subfamily Service Technical Bulletin Faboideae (Fabaceae) Number 1890 Volume I Joseph H. Kirkbride, Jr., Charles R. Gunn, and Anna L. Weitzman Fruits of A, Centrolobium paraense E.L.R. Tulasne. B, Laburnum anagyroides F.K. Medikus. C, Adesmia boronoides J.D. Hooker. D, Hippocrepis comosa, C. Linnaeus. E, Campylotropis macrocarpa (A.A. von Bunge) A. Rehder. F, Mucuna urens (C. Linnaeus) F.K. Medikus. G, Phaseolus polystachios (C. Linnaeus) N.L. Britton, E.E. Stern, & F. Poggenburg. H, Medicago orbicularis (C. Linnaeus) B. Bartalini. I, Riedeliella graciliflora H.A.T. Harms. J, Medicago arabica (C. Linnaeus) W. Hudson. Kirkbride is a research botanist, U.S. Department of Agriculture, Agricultural Research Service, Systematic Botany and Mycology Laboratory, BARC West Room 304, Building 011A, Beltsville, MD, 20705-2350 (email = [email protected]). Gunn is a botanist (retired) from Brevard, NC (email = [email protected]). Weitzman is a botanist with the Smithsonian Institution, Department of Botany, Washington, DC. Abstract Kirkbride, Joseph H., Jr., Charles R. Gunn, and Anna L radicle junction, Crotalarieae, cuticle, Cytiseae, Weitzman. 2003. Fruits and seeds of genera in the subfamily Dalbergieae, Daleeae, dehiscence, DELTA, Desmodieae, Faboideae (Fabaceae). U. S. Department of Agriculture, Dipteryxeae, distribution, embryo, embryonic axis, en- Technical Bulletin No. 1890, 1,212 pp. docarp, endosperm, epicarp, epicotyl, Euchresteae, Fabeae, fracture line, follicle, funiculus, Galegeae, Genisteae, Technical identification of fruits and seeds of the economi- gynophore, halo, Hedysareae, hilar groove, hilar groove cally important legume plant family (Fabaceae or lips, hilum, Hypocalypteae, hypocotyl, indehiscent, Leguminosae) is often required of U.S. -
TAXON:Neonotonia Wightii SCORE:16.0 RATING:High Risk
TAXON: Neonotonia wightii SCORE: 16.0 RATING: High Risk Taxon: Neonotonia wightii Family: Fabaceae Common Name(s): glycine Synonym(s): Glycine wightii (Wight & Arn.) Verdc. perennial soybean Notonia wightii Wight & Arn. soja pérenne soja-perene Assessor: Chuck Chimera Status: Assessor Approved End Date: 4 May 2015 WRA Score: 16.0 Designation: H(HPWRA) Rating: High Risk Keywords: Fodder Plant, Smothering Vine, N-Fixing, Self-Compatible, Animal-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 y 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 303 Agricultural/forestry/horticultural weed n=0, y = 2*multiplier (see Appendix 2) n 304 Environmental weed n=0, y = 2*multiplier (see Appendix 2) y 305 Congeneric weed n=0, y = 1*multiplier (see Appendix 2) n 401 Produces spines, thorns -
Rbcl and Legume Phylogeny, with Particular Reference to Phaseoleae, Millettieae, and Allies Tadashi Kajita; Hiroyoshi Ohashi; Yoichi Tateishi; C
rbcL and Legume Phylogeny, with Particular Reference to Phaseoleae, Millettieae, and Allies Tadashi Kajita; Hiroyoshi Ohashi; Yoichi Tateishi; C. Donovan Bailey; Jeff J. Doyle Systematic Botany, Vol. 26, No. 3. (Jul. - Sep., 2001), pp. 515-536. Stable URL: http://links.jstor.org/sici?sici=0363-6445%28200107%2F09%2926%3A3%3C515%3ARALPWP%3E2.0.CO%3B2-C Systematic Botany is currently published by American Society of Plant Taxonomists. Your use of the JSTOR archive indicates your acceptance of JSTOR's Terms and Conditions of Use, available at http://www.jstor.org/about/terms.html. JSTOR's Terms and Conditions of Use provides, in part, that unless you have obtained prior permission, you may not download an entire issue of a journal or multiple copies of articles, and you may use content in the JSTOR archive only for your personal, non-commercial use. Please contact the publisher regarding any further use of this work. Publisher contact information may be obtained at http://www.jstor.org/journals/aspt.html. Each copy of any part of a JSTOR transmission must contain the same copyright notice that appears on the screen or printed page of such transmission. The JSTOR Archive is a trusted digital repository providing for long-term preservation and access to leading academic journals and scholarly literature from around the world. The Archive is supported by libraries, scholarly societies, publishers, and foundations. It is an initiative of JSTOR, a not-for-profit organization with a mission to help the scholarly community take advantage of advances in technology. For more information regarding JSTOR, please contact [email protected]. -
Abstract PARSING POLYPHYLETIC PUERARIA: DELIMITING DISTINCT
Abstract PARSING POLYPHYLETIC PUERARIA: DELIMITING DISTINCT EVOLUTIONARY LINEAGES THROUGH PHYLOGENY by William Cagle May, 2013 Director: Dr. Ashley N. Egan DEPARTMENT OF BIOLOGY A taxon is defined as polyphyletic when it does not include the last common ancestor of all true members of the taxon, resulting in a number of subgroups not united by a common ancestor. Previous work has suggested Pueraria (Fabaceae) to be polyphyletic. Although several taxonomic treatments have recognized Pueraria as an unnatural grouping since its creation in 1825, and two have put forth taxonomic hypotheses, the polyphyly has never been resolved. The need for further biosystematic research has always been cited as the reason no changes were proposed. This project attempted to address this issue by sampling broadly across phaseoloid legumes with an initial target goal of 156 species including 15 species of Pueraria. Ultimately, 104 species across 69 genera were sampled for AS2 and 116 species across 64 genera for matK. Phylogeny reconstruction was carried out using maximum likelihood and Bayesian inference. Both analyses yielded congruent tree topologies and similar support values. Both previous taxonomic hypotheses show some congruence with the data, but discrepancies do occur. This work provides strong support for the existence of five separate clades within the genus Pueraria, requiring the resurrection of the genus Neustanthus for P. phaseoloides along with the need to create a new genus each for P. stricta, P. peduncularis, and P. wallichii. PARSING POLYPHYLETIC PUERARIA: DELIMITING DISTINCT EVOLUTIONARY LINEAGES THROUGH PHYLOGENY A Thesis Presented to The Faculty of the Department of Biology East Carolina University In Partial Fulfillment of the Requirements for the Degree Master of Science in Biology by William Cagle May 2013 © William Cagle, 2013 PARSING POLYPHYLETIC PUERARIA: DELIMITING DISTINCT EVOLUTIONARY LINEAGES THROUGH PHYLOGENY by William Cagle APPROVED BY: DIRECTOR OF DISSERTATION/THESIS __________________________________________ Ashley N. -
3.3.2.1. Familia Fabaceae O Leguminosae
122 3.3.2.1. Familia Fabaceae o Leguminosae La familia Fabaceae es considerada claramente monofilética en análisis tanto moleculares como morfológicos, sin embargo según Takhtajan 1997 era tratada como tres familias distintas. En las actuales reconstrucciones de filogenia, la subfamilia Caesalpinioideae es considerada parafilética, mientras que las subfamilias Mimosoideae y Faboideae (o Papilionoideae) son consideradas monofiléticas. Sin embargo, actualmente el reconocimiento de la subfamilia Caesalpinoideae se mantiene por razones meramente prácticas. (Steven, 2009) Los estudios filogenéticos llevados a cabo hasta el momento no fueron suficientes para la elaboración de una clasificación aceptable a nivel de subfamilias en Fabaceae. De cualquier forma es evidente que la subfamilia Caesalpinoideae al ser considerada parafilética debe ser redefinida. Así uno de los grupos que aparece claramente disociado de las Caesalpinoideae es Cercideae, al cual pertenece el género Bauhinia. Sin embargo es muy prematuro el reconocimiento de nuevos grupos formalmente (Lewis, 2005). Lo que queda claro hasta el momento es que el número de subfamilias dentro de Fabaceae debe ser superior de las tres tradicionalmente reconocidas y que el clado Cercideae podrá constituir una de las nuevas subfamilias.(Souza & Lorenzi, 2008) A nivel de familia, las leguminosas se encuentran cercanamente relacionadas con las familias Polygalaceae, Suraniaceae y Quillajaceae, las cuales forman el orden Fabales (Stevens, 2001) Clave artificial para el reconocimiento de las subfamilias 1. Flores actinomorfas, que forman capítulos, espigas o racimos. Corola con prefloración valvar y con frecuencia gamopétala. Estambres 4-8-∝, sobrepasando la corola; filamentos libres. Polen frecuentemente en políadas. Semillas con línea fisural. I. Mimosoideae 1`. Flores zigomorfas, generalmente en racimos. -
A New Subfamily Classification of The
LPWG Phylogeny and classification of the Leguminosae TAXON 66 (1) • February 2017: 44–77 A new subfamily classification of the Leguminosae based on a taxonomically comprehensive phylogeny The Legume Phylogeny Working Group (LPWG) Recommended citation: LPWG (2017) This paper is a product of the Legume Phylogeny Working Group, who discussed, debated and agreed on the classification of the Leguminosae presented here, and are listed in alphabetical order. The text, keys and descriptions were written and compiled by a subset of authors indicated by §. Newly generated matK sequences were provided by a subset of authors indicated by *. All listed authors commented on and approved the final manuscript. Nasim Azani,1 Marielle Babineau,2* C. Donovan Bailey,3* Hannah Banks,4 Ariane R. Barbosa,5* Rafael Barbosa Pinto,6* James S. Boatwright,7* Leonardo M. Borges,8* Gillian K. Brown,9* Anne Bruneau,2§* Elisa Candido,6* Domingos Cardoso,10§* Kuo-Fang Chung,11* Ruth P. Clark,4 Adilva de S. Conceição,12* Michael Crisp,13* Paloma Cubas,14* Alfonso Delgado-Salinas,15 Kyle G. Dexter,16* Jeff J. Doyle,17 Jérôme Duminil,18* Ashley N. Egan,19* Manuel de la Estrella,4§* Marcus J. Falcão,20 Dmitry A. Filatov,21* Ana Paula Fortuna-Perez,22* Renée H. Fortunato,23 Edeline Gagnon,2* Peter Gasson,4 Juliana Gastaldello Rando,24* Ana Maria Goulart de Azevedo Tozzi,6 Bee Gunn,13* David Harris,25 Elspeth Haston,25 Julie A. Hawkins,26* Patrick S. Herendeen,27§ Colin E. Hughes,28§* João R.V. Iganci,29* Firouzeh Javadi,30* Sheku Alfred Kanu,31 Shahrokh Kazempour-Osaloo,32* Geoffrey C. -
ISTA List of Stabilized Plant Names 6Th Edition
ISTA List of Stabilized Plant Names 6th Edition ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema Published by All rights reserved. No part of this publication may The International Seed Testing Association (ISTA) be reproduced, stored in any retrieval system or Zürichstr. 50, CH-8303 Bassersdorf, Switzerland transmitted in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, ©2014 International Seed Testing Association (ISTA) without prior permission in writing from ISTA. ISBN 978-3-906549-77-4 ISTA List of Stabilized Plant Names 1st Edition 1966 ISTA Nomenclature Committee Chair: Prof. P. A. Linehan 2nd Edition 1983 ISTA Nomenclature Committee Chair: Dr. H. Pirson 3rd Edition 1988 ISTA Nomenclature Committee Chair: Dr. W. A. Brandenburg 4th Edition 2001 ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema 5th Edition 2007 ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema 6th Edition 2013 ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema ii 6th Edition 2013 ISTA List of Stabilized Plant Names Contents Contents Preface ...................................................... iv L ................................................................41 Acknowledgements .................................... v M ...............................................................46 Symbols and abbreviations ....................... vi N ...............................................................50 ISTA List of Stabilized Plant Names ........... 1 O ...............................................................51 -
Classification and Botanical Description of Legumes
Halley Allaire Taylor Brady Classification and Botanical Description of Legumes Legumes, or pulses, are flowering plants in the Leguminosae family. The word legume is derived from the Latin verb legere which means to gather. The term pulse has a more direct lineage. It derives from puls or porridge, a cooked bean dish which the ancient Romans were fond of eating. (Albala 7). This family is also known as Fabaceae, and both terms can be used interchangeably to indicate the some 690 genera and 18,000 species therein (Morris 365). The Leguminosae family is classified into three sub-families: Papilionoideae, Caesalpinioideae, and Mimosoideae. Each sub-family is identified by its flowers. Edible legume crops are mainly found in the sub-family Papilionoideae. This includes the soybean, chickpea, bean, and pea, among others (Morris 365). Other lesser known members of the legume family include clover, licorice, lentils, and the peanut. The peanut is in fact, biologically though not culinarily, defined as a woody, indehiscent legume. Unique to Fabaceae are the flowers and fruit. Like many flowers, those found on legume plants are hermaphroditic, containing both the stamen and pistil. This makes the plants self- fertile, meaning that an individual plant is able to reproduce by itself which can have the effect of limiting genetic diversity. However, hybridization occurs frequently in nature due to this characteristic, as any plant can pollinate another due to the hermaphroditic properties therein (Weaver 57). This creates difficulty in clearly defining the differences that enter between subspecies. The flower typically has five petals and an ovary with one carpel, cavity, and style (Morris 365). -
Relationships Among Phaseoloid Legumes Based on Sequences from Eight Chloroplast Regions
Systematic Botany (2009), 34(1): pp. 115–128 © Copyright 2009 by the American Society of Plant Taxonomists Relationships Among Phaseoloid Legumes Based on Sequences from Eight Chloroplast Regions Saša Stefanovic´, 1, 6 Bernard E. Pfeil, 2, 6 Jeffrey D. Palmer, 3 and Jeff J. Doyle 4, 5 1Department of Biology, University of Toronto, Mississauga, Ontario L5L 1C6 Canada 2CSIRO & Centre for Plant Biodiversity Research, GPO Box 1600, Canberra ACT 2601 Australia 3Department of Biology, Indiana University, Bloomington, Indiana 47405 U.S.A. 4Department of Plant Biology, 228 Plant Science Building, Cornell University, Ithaca, New York 14853 U.S.A. 5 Author for correspondence ( [email protected] ) 6 These authors contributed equally to this study Communicating Editor: Alan W. Meerow Abstract— Generic level relationships in phaseoloid legumes have received much attention using chloroplast DNA markers. However, despite this attention not all relationships are yet well-resolved. This study includes trnL-F sequences from across a wide sample of phaseoloid legumes as well as seven additional chloroplast DNA loci ( rbcL, atpB, trnK/matK, rpl2, clpP, rps16, and ycf4 ) analyzed separately and in combi- nation. Together, these data provide support for many relationships generally consistent with, but only weakly supported, in earlier studies. Some major discordant phylogenetic results were found in our separate analyses; for example, ycf4 sequences group Glycine and Teramnus with strong support; however, the combined analysis of the remaining seven loci found incongruent groupings (Glycine and Psoraleeae genera; Teramnus and Amphicarpaea ) also with strong support. Network analysis of ycf4 revealed that the conflicting signal (relative to the other seven loci) came from first and second codon positions. -
Microsoft Word
Subfamily Faboideae Scientific Classification Kingdom: Plantae Subkingdom: Tracheobionta (Vascular plants/Piante vascolari) Superdivision: Spermatophyta (Seed plants/Piante con semi) Division: Magnoliophyta (Flowering plants/Piante con fiori) Class: Rosopsida Batsch, 1788 Subclass: Rosidae Takht., 1967 SuperOrder: Fabanae R. Dahlgren ex Reveal, 1993 Order: Fabales Family: Fabaceae o Papilionacee Subfamily: Faboideae o Papilionoideae Faboideae is a subfamily of the flowering plant family Fabaceae . An acceptable alternative name for the subfamily is Papilionoideae . This subfamily is widely distributed and members are adapted to a wide variety of environments. Faboideae may be trees, shrubs or herbs. The flowers are classically pea shaped and root nodulation is very common. Flowers: Zygomorphic, papilionaceous; hypan-thium present; petals 5 [1 banner or standard petal outermost, 2 free lateral wing petals, and 2 petals fused to form the keel]; stamens 10, usually diadelphous (9 connate, 1 free), sometimes monadelphous or all free Inflorescences: Racemes, spikes, or heads Fruits: Diverse legumes Seeds: Without endosperm; lacking pleurogram Habit: Mostly herbs, some trees and shrubs; temperate, subtropical, and tropical Leaves: Usually pinnately compound, sometimes palmately compound, rarely simple, alternate, with stipules The belonging genera to the Faboideae family are: • Abrus • Craspedolobium • Kummerowia • Podalyria • Acosmium • Cratylia • Lablab • Podocytisus • Adenocarpus • Crotalaria • Laburnum • Poecilanthe • Adenodolichos • Cruddasia -
Supp Material.Pdf
Supplementary Information Localized hypermutation and associated gene losses in legume chloroplast genomes Alan M. Magee1, Sue Aspinall2, Danny W. Rice3, Brian P. Cusack1, Marie Sémon4, Antoinette S. Perry1, Sasa Stefanovic5, Dan Milbourne6, Susanne Barth6, Jeffrey D. Palmer3, John C. Gray2, Tony A. Kavanagh1, and Kenneth H. Wolfe1 1 Smurfit Institute of Genetics, Trinity College, Dublin 2, Ireland 2 Department of Plant Sciences, University of Cambridge, Downing Street, Cambridge CB2 3EA, United Kingdom 3 Department of Biology, Indiana University, Bloomington, Indiana 47405 4 Institut de Génomique Fonctionnelle de Lyon, Université de Lyon, CNRS, INRA, UCB Lyon 1, Ecole Normale Supérieure de Lyon, 69364 Lyon Cedex 07, France 5 Department of Biology, University of Toronto, Mississauga, Ontario L5L 1C6, Canada 6 Teagasc Crops Research Centre, Oak Park, Carlow, Ireland Supplementary Figure legends Figure S1. Synonymous and nonsynonymous divergence in angiosperm chloroplast matK (A), rbcL (B), and ycf4 (C) genes. The trees are the same as those in Figure 1, except for the addition of taxon names. Shown are dN (left) and dS (right) trees resulting from a codon-based likelihood analysis and a constrained topology, rooted using gymnosperm sequences (which are not included in the trees). See Methods for details of tree construction. The species are in the same order from top to bottom in all trees to the greatest extent possible. In (C), numbers after species names indicate the ycf4 gene length in codons. The ycf4 pseudogenes in Desmodium and Clitoria are included in the ycf4 trees and labeled in the left panel. The Lathyrus odoratus and Pisum sativum ycf4 pseudogenes were not included in the tree because they are truncated and very divergent, making their boundaries hard to define. -
(Diceros Bicornis Michaeli) in Southern Serengeti National Park, Tanzania
The Feeding Ecology of Eastern Black Rhinoceroses (Diceros bicornis michaeli) in southern Serengeti national Park, Tanzania. Philbert Ngoti Natural Resources Management Submission date: June 2017 Supervisor: Bente Jessen Graae, IBI Norwegian University of Science and Technology Department of Biology MASTERS THESIS NTNU – TRONDHEIM Norwegian University of Science and Technology FEEDING ECOLOGY OF EASTERN BLACK RHINOCEROS (DICEROS BICORNIS MICHAELI) IN SOUTHERN SERENGETI NATIONAL PARK, TANZANIA PHILBERT MICHAEL NGOTI Natural Resources Management (Biology) Submission date: June 2017 Supervisors Prof. Bente Jessen Graae, NTNU, IBI, Main Supervisor Prof. James Mervyn Speed, NTNU, Co-supervisor Prof. T. Michael Anderson, Wake Forest University, USA Norwegian University of Science and Technology Department of Biology TABLE OF CONTENTS DEDICATION ................................................................................................................................ ii ACKNOWLEDGEMENT ............................................................................................................. iii ABSTRACT .................................................................................................................................... v INTRODUCTION .......................................................................................................................... 1 OBJECTIVES ................................................................................................................................. 2 METHODS ....................................................................................................................................