CATALOGUE of the GRASSES of CUBA by A. S. Hitchcock
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The Plant Press
Special Symposium Issue continues on page 14 Department of Botany & the U.S. National Herbarium The Plant Press New Series - Vol. 20 - No. 3 July-September 2017 Botany Profile Plant Expeditions: History Has Its Eyes On You By Gary A. Krupnick he 15th Smithsonian Botani- as specimens (living or dried) in centuries field explorers to continue what they are cal Symposium was held at the past. doing. National Museum of Natural The symposium began with Laurence T he morning session began with a History (NMNH) and the U.S. Botanic Dorr (Chair of Botany, NMNH) giv- th Garden (USBG) on May 19, 2017. The ing opening remarks. Since the lectures series of talks focusing on the 18 symposium, titled “Exploring the Natural were taking place in Baird Auditorium, Tcentury explorations of Canada World: Plants, People and Places,” Dorr took the opportunity to talk about and the United States. Jacques Cayouette focused on the history of plant expedi- the theater’s namesake, Spencer Baird. A (Agriculture and Agri-Food Canada) tions. Over 200 participants gathered to naturalist, ornithologist, ichthyologist, and presented the first talk, “Moravian Mis- hear stories dedicated col- sionaries as Pioneers of Botanical Explo- and learn about lector, Baird was ration in Labrador (1765-1954).” He what moti- the first curator explained that missionaries of the Mora- vated botanical to be named vian Church, one of the oldest Protestant explorers of at the Smith- denominations, established missions the Western sonian Institu- along coastal Labrador in Canada in the Hemisphere in the 18th, 19th, and 20th tion and eventually served as Secretary late 1700s. -
Plants Prohibited from Sale in South Australia Plants Considered As Serious Weeds Are Banned from Being Sold in South Australia
Plants prohibited from sale in South Australia Plants considered as serious weeds are banned from being sold in South Australia. Do not buy or sell any plant listed as prohibited from sale. Plants listed in this document are declared serious weeds and are prohibited from sale anywhere in South Australia pursuant to Section 188 of the Landscape South Australia Act 2019 (refer South Australian Government Gazette 60: 4024-4038, 23 July 2020). This includes the sale of nursery stock, seeds or other propagating material. However, it is not prohibited to sell or transport non-living products made from these plants, such as timber from Aleppo pine, or herbal medicines containing horehound. Such products are excluded from the definition of plant, under the Landscape South Australia (General) Regulations 2020. Section 3 of the Act defines sell as including: • barter, offer or attempt to sell • receive for sale • have in possession for sale • cause or permit to be sold or offered for sale • send, forward or deliver for sale • dispose of by any method for valuable consideration • dispose of to an agent for sale on consignment • sell for the purposes of resale How to use this list Plants are often known by many names. This list can help you to find the scientific name and other common names of a declared plant. This list is not intended to be a complete synonymy for each species, such as would be found in a taxonomic revision. The plants are listed alphabetically by the common name as used in the declaration. Each plant is listed in the following format: Common name alternative common name(s) Scientific name Author Synonym(s) Author What to do if you suspect a plant for sale is banned If you are unsure whether a plant offered for sale under a particular name is banned, please contact your regional landscape board or PIRSA Biosecurity SA. -
Illustrated Flora of East Texas --- Taxa in Volume 1 (May 2004)
Illustrated Flora of East Texas --- Taxa in Volume 1 (May 2004) Family Genus Species Var. or Subsp. Native or Intro Ferns & Fern Allies Psilotaceae Psilotum nudum N Isoetaceae Isoetes butleri N Isoetaceae Isoetes melanopoda N Lycopodiaceae Lycopodiella alopecuroides N Lycopodiacae Lycopodiella appressa N Lycopodiaceae Lycopodiella prostrata N Lycopodiaceae Palhinhaea cernua N Lycopodiaceae Pseudolycopodiella caroliniana N Selaginellaceae Selaginella apoda var. apoda N Selaginellaceae Selaginella arenicola subsp. riddellii N Equisetaceae Equisetum hyemale subsp. affine N Equisetaceae Equisetum laevigatum N Anemiaceae Anemia mexicana N Aspleniaceae Asplenium platyneuron N Aspleniaceae Asplenium resiliens N Azollaceae Azolla caroliniana N Azollaceae Azolla mexicana N Blechnaceae Woodwardia areolata N Blechnaceae Woodwardia virginica N Dennstaedtiaceae Pteridium aquilinum var. pseudocaudatum N Dryopteridaceae Athyrium filix-femina subsp. asplenioides N Dryopteridaceae Cyrtomium falcatum I Dryopteridaceae Cystopteris protrusa N Dryopteridaceae Dryopteris celsa N Dryopteridaceae Dryopteris ludoviciana N Dryopteridaceae Nephrolepis exaltata I Dryopteridaceae Onoclea sensibilis N Dryopteridaceae Polystichum acrostichoides N Dryopteridaceae Tectaria heracleifolia N Dryopteridaceae Woodsia obtusa subsp. obtusa N Dryopteridaceae Woodsia obtusa subsp. occidentalis N Lygodiaceae Lygodium japonicum I Marsileaceae Marsilea macropoda N Marsileaceae Marsilea vestita N Marsileaceae Pilularia americana N Ophioglossaceae Botrychium biternatum N Ophioglossaceae -
Poaceae: Bambusoideae) Christopher Dean Tyrrell Iowa State University
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 2008 Systematics of the neotropical woody bamboo genus Rhipidocladum (Poaceae: Bambusoideae) Christopher Dean Tyrrell Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Botany Commons Recommended Citation Tyrrell, Christopher Dean, "Systematics of the neotropical woody bamboo genus Rhipidocladum (Poaceae: Bambusoideae)" (2008). Retrospective Theses and Dissertations. 15419. https://lib.dr.iastate.edu/rtd/15419 This Thesis is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Systematics of the neotropical woody bamboo genus Rhipidocladum (Poaceae: Bambusoideae) by Christopher Dean Tyrrell A thesis submitted to the graduate faculty in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE Major: Ecology and Evolutionary Biology Program of Study Committee: Lynn G. Clark, Major Professor Dennis V. Lavrov Robert S. Wallace Iowa State University Ames, Iowa 2008 Copyright © Christopher Dean Tyrrell, 2008. All rights reserved. 1457571 1457571 2008 ii In memory of Thomas D. Tyrrell Festum Asinorum iii TABLE OF CONTENTS ABSTRACT iv CHAPTER 1. GENERAL INTRODUCTION 1 Background and Significance 1 Research Objectives 5 Thesis Organization 6 Literature Cited 6 CHAPTER 2. PHYLOGENY OF THE BAMBOO SUBTRIBE 9 ARTHROSTYLIDIINAE WITH EMPHASIS ON RHIPIDOCLADUM Abstract 9 Introduction 10 Methods and Materials 13 Results 19 Discussion 25 Taxonomic Treatment 26 Literature Cited 31 CHAPTER 3. -
Creation and Carnivory in the Pitcher Plants of Nepenthaceae and Sarraceniaceae
OPEN ACCESS JCTS Article SERIES B Creation and Carnivory in the Pitcher Plants of Nepenthaceae and Sarraceniaceae R.W. Sanders and T.C. Wood Core Academy of Science, Dayton, TN Abstract The morphological adaptations of carnivorous plants and taxonomic distributions of those adaptations are reviewed, as are the conflicting classifications of the plants based on the adaptations, reproductive morphology, and DNA sequences. To begin developing a creationist understanding of the origin of plant carnivory, we here focus specifically on pitcher plants of Nepenthaceae and Sarraceniaceae because their popularity as cultivated curiosities has generated a literature resource amenable to baraminological analysis. Hybridization records were augmented by total nucleotide differences to assess species similarities. Nonhybridizing species falling within the molecular range of hybridizing species were included in the monobaramin of the hybridizing species. The combined data support each of the three genera of the Sarraceniaceae as a monobaramin, but the three could not be combined into a larger monobaramin. With the Nepenthaceae, the data unequivocally place 73% of the species in a single monobaramin, strongly suggesting the whole genus (and, thus, family) is a monobaramin. The lack of variation in the carnivorous habit provides no evidence for the intrabaraminic origin of carnivory from non-carnivorous plants. An array of fascinating symbiotic relationships of pitchers in some species with unusual bacteria, insects, and vertebrates are known and suggest the origin of carnivory from benign functions of the adaptive structures. However, these symbioses still do not account for the apparent complex design for carnivory characteristic of all species in the two families. Editor: J.W. -
Types of American Grasses
z LIBRARY OF Si AS-HITCHCOCK AND AGNES'CHASE 4: SMITHSONIAN INSTITUTION UNITED STATES NATIONAL MUSEUM oL TiiC. CONTRIBUTIONS FROM THE United States National Herbarium Volume XII, Part 3 TXE&3 OF AMERICAN GRASSES . / A STUDY OF THE AMERICAN SPECIES OF GRASSES DESCRIBED BY LINNAEUS, GRONOVIUS, SLOANE, SWARTZ, AND MICHAUX By A. S. HITCHCOCK z rit erV ^-C?^ 1 " WASHINGTON GOVERNMENT PRINTING OFFICE 1908 BULLETIN OF THE UNITED STATES NATIONAL MUSEUM Issued June 18, 1908 ii PREFACE The accompanying paper, by Prof. A. S. Hitchcock, Systematic Agrostologist of the United States Department of Agriculture, u entitled Types of American grasses: a study of the American species of grasses described by Linnaeus, Gronovius, Sloane, Swartz, and Michaux," is an important contribution to our knowledge of American grasses. It is regarded as of fundamental importance in the critical sys- tematic investigation of any group of plants that the identity of the species described by earlier authors be determined with certainty. Often this identification can be made only by examining the type specimen, the original description being inconclusive. Under the American code of botanical nomenclature, which has been followed by the author of this paper, "the nomenclatorial t}rpe of a species or subspecies is the specimen to which the describer originally applied the name in publication." The procedure indicated by the American code, namely, to appeal to the type specimen when the original description is insufficient to identify the species, has been much misunderstood by European botanists. It has been taken to mean, in the case of the Linnsean herbarium, for example, that a specimen in that herbarium bearing the same name as a species described by Linnaeus in his Species Plantarum must be taken as the type of that species regardless of all other considerations. -
Vascular Plants of Williamson County Leersia Hexandra Swartz
Vascular Plants of Williamson County Leersia hexandra − CLUBHEAD CUTGRASS [Poaceae] Leersia hexandra Swartz, CLUBHEAD CUTGRASS. Aquatic perennial herb, clonal, with submersed, short-lived rhizomes and stolon-bearing, fibrous-rooted, not rosetted, shoots in sparse clones with stolons arising from mother plant, mother plant rooted from short rhizome having several emergent shoots, stolons submersed and horizontal initially with 1 emergent shoot at a node, in range to 35 cm tall; flowering shoot with several basal leaves including at least 2 with photosynthetic blades and ca. 4 cauline leaves, axes with hairs at nodes, conspicuously scabrous, shoot unbranched with terminal inflorescence or with an ascending lateral shoot from an axillary bud above midplant; rhizomes poorly defined with many adventitious roots; stolons (termed rhizomes by other authors) with long, slender internodes, to 30 × ca. 0.7 mm, with 1−3 adventitious roots per node with or without an emergent shoot. Stems: cylindric, hidden by sheaths, internodes smooth, nodes purple- red, appearing channeled to flattened, to 2 mm diameter, having dense, stiff, appressed downward-pointing hairs (incl. basal of leaf sheath) with hirsute hairs to 1 mm long. Leaves: alternate distichous, simple with sheath; prophyll at base of emergent shoot of mother plant, to 10 mm long, membranous, light red-purple, appearing open, conspicuously 2-keeled with wide membranous margins, with sparse minute teeth along keels; sheath open but tightly sealed around stems, sheaths often with sparse, minute -
24. Tribe PANICEAE 黍族 Shu Zu Chen Shouliang (陈守良); Sylvia M
POACEAE 499 hairs, midvein scabrous, apex obtuse, clearly demarcated from mm wide, glabrous, margins spiny-scabrous or loosely ciliate awn; awn 1–1.5 cm; lemma 0.5–1 mm. Anthers ca. 0.3 mm. near base; ligule ca. 0.5 mm. Inflorescence up to 20 cm; spike- Caryopsis terete, narrowly ellipsoid, 1–1.8 mm. lets usually densely arranged, ascending or horizontally spread- ing; rachis scabrous. Spikelets 1.5–2.5 mm (excluding awns); Stream banks, roadsides, other weedy places, on sandy soil. Guangdong, Hainan, Shandong, Taiwan, Yunnan [Bhutan, Cambodia, basal callus 0.1–0.2 mm, obtuse; glumes narrowly lanceolate, India, Indonesia, Laos, Malaysia, Myanmar, Nepal, Philippines, Sri back scaberulous-hirtellous in rather indistinct close rows (most Lanka, Thailand, Vietnam; Africa (probably introduced), Australia obvious toward lemma base), midvein pectinate-ciliolate, apex (Queensland)]. abruptly acute, clearly demarcated from awn; awn 0.5–1.5 cm. Anthers ca. 0.3 mm. Caryopsis terete, narrowly ellipsoid, ca. 3. Perotis hordeiformis Nees in Hooker & Arnott, Bot. Beech- 1.5 mm. Fl. and fr. summer and autumn. 2n = 40. ey Voy. 248. 1838. Sandy places, along seashores. Guangdong, Hebei, Jiangsu, 麦穗茅根 mai sui mao gen Yunnan [India, Indonesia, Malaysia, Nepal, Myanmar, Pakistan, Sri Lanka, Thailand]. Perotis chinensis Gandoger. This species is very close to Perotis indica and is sometimes in- Annual or short-lived perennial. Culms loosely tufted, cluded within it. No single character by itself is reliable for separating erect or decumbent at base, 25–40 cm tall. Leaf sheaths gla- the two, but the combination of characters given in the key will usually brous; leaf blades lanceolate to narrowly ovate, 2–4 cm, 4–7 suffice. -
Geographic Origins, Genetic Diversity and the Molecular Clock Hypothesis in the Oryzeae
Geographic Origins, Genetic Diversity and the Molecular Clock Hypothesis in the Oryzeae G. SECQMD Biologie des Populations et des Peuplements, Centre Louis Emberger, C.N.R. S,, B.P. 5051 ., F-34033 Montpellier Cedex (France). And Institut Français de Recherche Scientifique pour le Développement en Coopération (ORSTOM), 24 rue Bayard. 75008 Paris. ABSTRACT The two species groups,Sativa and Latifolia of the genus Oryza seem to be genetically independant in their variation. They have both a pan-tropical distribution. A study using isozyme electrophoresis of strains representing most of the area of distribution at 16 to 40 loci, shows a genetic structure in disagreement with that previously established on a morphological basis (Morishima 1969 and others). The isozyme structure shows, fn both groups, a maximum divergence between Australian and other taxa, while American taxa are closely related to theis Asian counterparts. The application of the calibration of the electrophoretic clock by Sapich (1977) to the distances found points to a tlme of divergence for the Australian taxa compatible with geological data of a collision between Australasia and South-East Asia some 15 millions $years ago. The same calibration gives estimates compatible with OUT knowledge on the palaeoenvironment in particular with regards to : 1)- The possibilities of migration between Eurasia and Africa (interrupted earlier for species of rice adapted to forest or inundated plain than for those species adapted to temporary pools in arid savannas) 2)- The emergence of the Himalayan barrier between China and South Asia. The evolutionary picture which emerges ia that of an Eurasian Y Fonds i-i-ieíTL3i RSTO 1 DoGu 6 M c NATO AS1Series, Vol. -
Arundinelleae; Panicoideae; Poaceae)
Bothalia 19, 1:45-52(1989) Kranz distinctive cells in the culm of ArundineUa (Arundinelleae; Panicoideae; Poaceae) EVANGELINA SANCHEZ*, MIRTA O. ARRIAGA* and ROGER P. ELLIS** Keywords: anatomy, Arundinella, C4, culm, distinctive cells, double bundle sheath, NADP-me ABSTRACT The transectional anatomy of photosynthetic flowering culms of Arundinella berteroniana (Schult.) Hitchc. & Chase and A. hispida (Willd.) Kuntze from South America and A. nepalensis Trin. from Africa is described and illustrated. The vascular bundles are arranged in three distinct rings, the outermost being external to a continuous sclerenchymatous band. Each of these peripheral bundles is surrounded by two bundle sheaths, a complete mestome sheath and an incomplete, outer, parenchymatous Kranz sheath, the cells of which contain large, specialized chloroplasts. Kranz bundle sheath extensions are also present. The chlorenchyma tissue is also located in this narrow peripheral zone and is interrupted by the vascular bundles and their associated sclerenchyma. Dispersed throughout the chlorenchyma are small groups of Kranz distinctive cells, identical in structure to the outer bundle sheath cells. No chlorenchyma cell is. therefore, more than two cells distant from a Kranz cell. The structure of the chlorenchyma and bundle sheaths indicates that the C4 photosynthetic pathway is operative in these culms. This study clearly demonstrates the presence of the peculiar distinctive cells in the culms as well as in the leaves of Arundinella. Also of interest is the presence of an inner bundle sheath in the vascular bundles of the culm whereas the bundles of the leaves possess only a single sheath. It has already been shown that Arundinella is a NADP-me C4 type and the anatomical predictor of a single Kranz sheath for NADP-me species, therefore, either does not hold in the culms of this genus or the culms are not NADP-me. -
Phylogeny and Subfamilial Classification of the Grasses (Poaceae) Author(S): Grass Phylogeny Working Group, Nigel P
Phylogeny and Subfamilial Classification of the Grasses (Poaceae) Author(s): Grass Phylogeny Working Group, Nigel P. Barker, Lynn G. Clark, Jerrold I. Davis, Melvin R. Duvall, Gerald F. Guala, Catherine Hsiao, Elizabeth A. Kellogg, H. Peter Linder Source: Annals of the Missouri Botanical Garden, Vol. 88, No. 3 (Summer, 2001), pp. 373-457 Published by: Missouri Botanical Garden Press Stable URL: http://www.jstor.org/stable/3298585 Accessed: 06/10/2008 11:05 Your use of the JSTOR archive indicates your acceptance of JSTOR's Terms and Conditions of Use, available at http://www.jstor.org/page/info/about/policies/terms.jsp. 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/action/showPublisher?publisherCode=mobot. 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. JSTOR is a not-for-profit organization founded in 1995 to build trusted digital archives for scholarship. We work with the scholarly community to preserve their work and the materials they rely upon, and to build a common research platform that promotes the discovery and use of these resources. For more information about JSTOR, please contact [email protected]. -
Checklist Das Spermatophyta Do Estado De São Paulo, Brasil
Biota Neotrop., vol. 11(Supl.1) Checklist das Spermatophyta do Estado de São Paulo, Brasil Maria das Graças Lapa Wanderley1,10, George John Shepherd2, Suzana Ehlin Martins1, Tiago Egger Moellwald Duque Estrada3, Rebeca Politano Romanini1, Ingrid Koch4, José Rubens Pirani5, Therezinha Sant’Anna Melhem1, Ana Maria Giulietti Harley6, Luiza Sumiko Kinoshita2, Mara Angelina Galvão Magenta7, Hilda Maria Longhi Wagner8, Fábio de Barros9, Lúcia Garcez Lohmann5, Maria do Carmo Estanislau do Amaral2, Inês Cordeiro1, Sonia Aragaki1, Rosângela Simão Bianchini1 & Gerleni Lopes Esteves1 1Núcleo de Pesquisa Herbário do Estado, Instituto de Botânica, CP 68041, CEP 04045-972, São Paulo, SP, Brasil 2Departamento de Biologia Vegetal, Instituto de Biologia, Universidade Estadual de Campinas – UNICAMP, CP 6109, CEP 13083-970, Campinas, SP, Brasil 3Programa Biota/FAPESP, Departamento de Biologia Vegetal, Instituto de Biologia, Universidade Estadual de Campinas – UNICAMP, CP 6109, CEP 13083-970, Campinas, SP, Brasil 4Universidade Federal de São Carlos – UFSCar, Rod. João Leme dos Santos, Km 110, SP-264, Itinga, CEP 18052-780, Sorocaba, SP, Brasil 5Departamento de Botânica – IBUSP, Universidade de São Paulo – USP, Rua do Matão, 277, CEP 05508-090, Cidade Universitária, Butantã, São Paulo, SP, Brasil 6Departamento de Ciências Biológicas, Universidade Estadual de Feira de Santana – UEFS, Av. Transnordestina, s/n, Novo Horizonte, CEP 44036-900, Feira de Santana, BA, Brasil 7Universidade Santa Cecília – UNISANTA, R. Dr. Oswaldo Cruz, 266, Boqueirão, CEP 11045-907,