Sobre Los Géneros Descritos Por Cavanilles
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Sistema De Clasificación Artificial De Las Magnoliatas Sinántropas De Cuba
Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver Tesis doctoral de la Univerisdad de Alicante. Tesi doctoral de la Universitat d'Alacant. 2007 Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver PROGRAMA DE DOCTORADO COOPERADO DESARROLLO SOSTENIBLE: MANEJOS FORESTAL Y TURÍSTICO UNIVERSIDAD DE ALICANTE, ESPAÑA UNIVERSIDAD DE PINAR DEL RÍO, CUBA TESIS EN OPCIÓN AL GRADO CIENTÍFICO DE DOCTOR EN CIENCIAS SISTEMA DE CLASIFICACIÓN ARTIFICIAL DE LAS MAGNOLIATAS SINÁNTROPAS DE CUBA Pedro- Pabfc He.r retira Qltver CUBA 2006 Tesis doctoral de la Univerisdad de Alicante. Tesi doctoral de la Universitat d'Alacant. 2007 Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver PROGRAMA DE DOCTORADO COOPERADO DESARROLLO SOSTENIBLE: MANEJOS FORESTAL Y TURÍSTICO UNIVERSIDAD DE ALICANTE, ESPAÑA Y UNIVERSIDAD DE PINAR DEL RÍO, CUBA TESIS EN OPCIÓN AL GRADO CIENTÍFICO DE DOCTOR EN CIENCIAS SISTEMA DE CLASIFICACIÓN ARTIFICIAL DE LAS MAGNOLIATAS SINÁNTROPAS DE CUBA ASPIRANTE: Lie. Pedro Pablo Herrera Oliver Investigador Auxiliar Centro Nacional de Biodiversidad Instituto de Ecología y Sistemática Ministerio de Ciencias, Tecnología y Medio Ambiente DIRECTORES: CUBA Dra. Nancy Esther Ricardo Ñapóles Investigador Titular Centro Nacional de Biodiversidad Instituto de Ecología y Sistemática Ministerio de Ciencias, Tecnología y Medio Ambiente ESPAÑA Dr. Andreu Bonet Jornet Piiofesjar Titular Departamento de EGdfegfe Universidad! dte Mearte CUBA 2006 Tesis doctoral de la Univerisdad de Alicante. Tesi doctoral de la Universitat d'Alacant. 2007 Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver I. INTRODUCCIÓN 1 II. ANTECEDENTES 6 2.1 Historia de los esquemas de clasificación de las especies sinántropas (1903-2005) 6 2.2 Historia del conocimiento de las plantas sinantrópicas en Cuba 14 III. -
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 -
Contents About This Booklet 2 1
Contents About this booklet 2 1. Why indigenous gardening? 3 Top ten reasons to use indigenous plants 3 Indigenous plants of Whitehorse 4 Where can I buy indigenous plants of Whitehorse? 4 2. Sustainable Gardening Principles 5 Make your garden a wildlife garden 6 3. Tips for Successful Planting 8 1. Plant selection 8 2. Pre-planting preparation 10 3. Planting technique 12 4. Early maintenance 14 4. Designing your Garden 16 Climbers 16 Hedges and borders 17 Groundcovers and fillers 17 Lawn alternatives 18 Feature trees 18 Screen plants 19 Damp & shady spots 19 Edible plants 20 Colourful flowers 21 5. 94 Species Indigenous to Whitehorse 23 6. Weeds of Whitehorse 72 7. Further Resources 81 8. Index of Plants 83 Alphabetically by Botanical Name 83 Alphabetically by Common Name 85 9. Glossary 87 1 In the spirit of About this booklet reconciliation, Whitehorse City Council This booklet has been written by Whitehorse acknowledges the City Council to help gardeners and landscapers Wurundjeri people as adopt sustainable gardening principles by using the traditional owners indigenous plants commonly found in Whitehorse. of the land now known The collective effort of residents gardening with as Whitehorse and pays indigenous species can make a big difference to respects to its elders preserving and enhancing our biodiversity. past and present. We would like to acknowledge the volunteers of the Blackburn & District Tree Preservation Society, Whitehorse Community Indigenous Plant Project Inc. (Bungalook Nursery) and Greenlink Box Hill Nursery for their efforts to protect and enhance the indigenous flora of Whitehorse. Information provided by these groups is included in this guide. -
Chromosome Numbers in Compositae, XII: Heliantheae
SMITHSONIAN CONTRIBUTIONS TO BOTANY 0 NCTMBER 52 Chromosome Numbers in Compositae, XII: Heliantheae Harold Robinson, A. Michael Powell, Robert M. King, andJames F. Weedin SMITHSONIAN INSTITUTION PRESS City of Washington 1981 ABSTRACT Robinson, Harold, A. Michael Powell, Robert M. King, and James F. Weedin. Chromosome Numbers in Compositae, XII: Heliantheae. Smithsonian Contri- butions to Botany, number 52, 28 pages, 3 tables, 1981.-Chromosome reports are provided for 145 populations, including first reports for 33 species and three genera, Garcilassa, Riencourtia, and Helianthopsis. Chromosome numbers are arranged according to Robinson’s recently broadened concept of the Heliantheae, with citations for 212 of the ca. 265 genera and 32 of the 35 subtribes. Diverse elements, including the Ambrosieae, typical Heliantheae, most Helenieae, the Tegeteae, and genera such as Arnica from the Senecioneae, are seen to share a specialized cytological history involving polyploid ancestry. The authors disagree with one another regarding the point at which such polyploidy occurred and on whether subtribes lacking higher numbers, such as the Galinsoginae, share the polyploid ancestry. Numerous examples of aneuploid decrease, secondary polyploidy, and some secondary aneuploid decreases are cited. The Marshalliinae are considered remote from other subtribes and close to the Inuleae. Evidence from related tribes favors an ultimate base of X = 10 for the Heliantheae and at least the subfamily As teroideae. OFFICIALPUBLICATION DATE is handstamped in a limited number of initial copies and is recorded in the Institution’s annual report, Smithsonian Year. SERIESCOVER DESIGN: Leaf clearing from the katsura tree Cercidiphyllumjaponicum Siebold and Zuccarini. Library of Congress Cataloging in Publication Data Main entry under title: Chromosome numbers in Compositae, XII. -
Bursaria Cayzerae (Pittosporaceae), a Vulnerable New Species from North-Eastern New South Wales, Australia
Volume 15: 81–85 ELOPEA Publication date: 18 September 2013 T dx.doi.org/10.7751/telopea2013011 Journal of Plant Systematics plantnet.rbgsyd.nsw.gov.au/Telopea • escholarship.usyd.edu.au/journals/index.php/TEL • ISSN 0312-9764 (Print) • ISSN 2200-4025 (Online) Bursaria cayzerae (Pittosporaceae), a vulnerable new species from north-eastern New South Wales, Australia Ian R. H. Telford1,4, F. John Edwards2 and Lachlan M. Copeland3 1Botany and N.C.W. Beadle Herbarium, School of Environmental and Rural Science, University of New England, Armidale, NSW 2351, Australia 2PO Box 179, South Grafton, NSW 2460, Australia 3Ecological Australia, 35 Orlando St, Coffs Harbour Jetty, NSW 2450, Australia 4Author for correspondence: [email protected] Abstract Bursaria cayzerae I.Telford & L.M.Copel. (Pittosporaceae), a species endemic to north-eastern New South Wales, is described. Its distribution is mapped, and habitat and conservation status discussed. The attributes of the new species, B. longisepala and B. spinosa, are compared. A key to species of Bursaria that occur in New South Wales, including this new species, is provided. Introduction Bursaria (Pittosporaceae) is an endemic Australian genus with currently seven named species. In eastern Australia, the most common taxon is Bursaria spinosa Cav. subsp. spinosa, plants of which may flower in their juvenile stage. These neotonous plants superficially resemble small-leaved, long-spined species such as B. longisepala Domin. Revisionary studies by Cayzer et al. (1999) showed B. longisepala s.str. to be restricted to the Blue Mountains; material from elsewhere mostly represented misidentifications of specimens of neotonous plants of B. spinosa subsp. -
The Purple Copper Butterfly (Paralucia Spinifera) Cultural Burning Program
The Purple Copper Butterfly (Paralucia spinifera) Cultural Burning Program - Ecological Report For the Local Land Services M J A D W E S C H ENVIRONMENTAL SERVICE SUPPORT This Ecological Report has been prepared by Raymond Mjadwesch (BAppSci) of Mjadwesch Environmental Service Support. The information contained herein is complete and correct to the best of my knowledge. This document has been prepared in good faith and on the basis that neither MESS nor its personnel are liable (whether by reason of negligence, lack of care or otherwise) to any person or entity for any damage or loss whatsoever which may occur in respect of any representation, statement or advice herein. Signed: 11th March 2016 Raymond Mjadwesch Consulting Ecologist Mjadwesch Environmental Service Support 26 Keppel Street BATHURST NSW 2795 ph/fax: email: [email protected] ABN: 72 878 295 925 Printed: 11th March 2016 NEAT Pty Ltd Acknowledgements: The LLS provided funding for this project through the save Our Species program; the LLS and community volunteers assisted with nocturnal caterpillar surveys; thank you for all the caterpillar-spotting Colleen Farrow, Liz Davis, Milton Lewis, Michelle Hines, Huw Evans, Peter Evans, Clare Kerr, Gerarda Mader, Chris Bailey, Jolyon Briggs, Nic Mason and Brett Farrow. Cover: The Purple Copper Butterfly (Paralucia spinifera) Table of Contents Introduction .............................................................................................................................. 6 Methodology ............................................................................................................................ -
Chromosome Numbers in the Polemoniaceae Representatives Of
1937 171 Chromosome Numbers in the Polemoniaceae By Walter S. Flory Division of Horticulture, Texas Agricultural Experiment Station This family is divided by systematists into two subfamilies. Cobaeoideae is composed of the genera Cantua, Huthia, and Cobaea which are tall shrubs, trees, or vines. The approximately fourteen other (herbaceous or low shrubby) genera comprise the subfamily Polemonioideae. From the standpoint of number of included species the most important of these latter genera are Gilia, Phlox, Polemo nium, and Collomia. The genera Phlox and Polemonium are each quite distinct and their species are seldom confused with those of other genera, but the remaining twelve genera of this subfamily apparently do not have taxonomic boundaries of equivalent distinctness. Certain species have been placed in one genus by one author, and in one or more different genera by others. The genus Gilia has been ex tended by some writers to include practically all species of the Polemonioideae outside of the genera Phlox and Polemonium. This was first pointed out to me by Professor Edgar T. Wherry who is making a taxonomic and geographic study of the Polemoniaceae, and was increasingly emphasized as literature sources and herbarium specimens were consulted and examined. It has been the purpose of the work herein presented to secure data on all obtainable polemoniaceous species with respect to chro mosome numbers, size, and general morphology. Especial attention has been given to securing information of significance from a taxono mic standpoint. Since several factors combine to make the immedi ate completion of the original program impossible it seems desirable, meanwhile, to present the accumulated data, together with suggested conclusions. -
ASHY DOGWEED (Thymophylla [=Dyssodia] Tephroleuca)
ASHY DOGWEED (Thymophylla [=Dyssodia] tephroleuca) 5-Year Review: Summary and Evaluation Photograph: Chris Best, USFWS U.S. Fish and Wildlife Service Corpus Christi Ecological Services Field Office Corpus Christi, Texas September 2011 1 FIVE YEAR REVIEW Ashy dogweed/Thymophylla tephroleuca Blake 1.0 GENERAL INFORMATION 1.1 Reviewers Lead Regional Office: Southwest Regional Office, Region 2 Susan Jacobsen, Chief, Threatened and Endangered Species, 505-248-6641 Wendy Brown, Endangered Species Recovery Coordinator, 505-248-6664 Julie McIntyre, Recovery Biologist, 505-248-6507 Lead Field Office: Corpus Christi Ecological Services Field Office Robyn Cobb, Fish and Wildlife Biologist, 361- 994-9005, ext. 241 Amber Miller, Fish and Wildlife Biologist, 361-994-9005, ext. 247 Cooperating Field Office: Austin Ecological Services Field Office Chris Best, Texas State Botanist, 512- 490-0057, ext. 225 1.2 Purpose of 5-Year Reviews: The U.S. Fish and Wildlife Service (Service or USFWS) is required by section 4(c)(2) of the Endangered Species Act (Act) to conduct a status review of each listed species once every five years. The purpose of a 5-year review is to evaluate whether or not the species’ status has changed since it was listed (or since the most recent 5-year review). Based on the 5-year review, we recommend whether the species should be removed from the list of endangered and threatened species, be changed in status from endangered to threatened, or be changed in status from threatened to endangered. Our original listing as endangered or threatened is based on the species’ status considering the five threat factors described in section 4(a)(1) of the Act. -
Phylogeny of Malpighiaceae: Evidence from Chloroplast NDHF and TRNL-F Nucleotide Sequences
Phylogeny of Malpighiaceae: Evidence from Chloroplast NDHF and TRNL-F Nucleotide Sequences The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citation Davis, Charles C., William R. Anderson, and Michael J. Donoghue. 2001. Phylogeny of Malpighiaceae: Evidence from chloroplast NDHF and TRNL-F nucleotide sequences. American Journal of Botany 88(10): 1830-1846. Published Version http://dx.doi.org/10.2307/3558360 Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:2674790 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA American Journal of Botany 88(10): 1830±1846. 2001. PHYLOGENY OF MALPIGHIACEAE: EVIDENCE FROM CHLOROPLAST NDHF AND TRNL-F NUCLEOTIDE SEQUENCES1 CHARLES C. DAVIS,2,5 WILLIAM R. ANDERSON,3 AND MICHAEL J. DONOGHUE4 2Department of Organismic and Evolutionary Biology, Harvard University Herbaria, 22 Divinity Avenue, Cambridge, Massachusetts 02138 USA; 3University of Michigan Herbarium, North University Building, Ann Arbor, Michigan 48109-1057 USA; and 4Department of Ecology and Evolutionary Biology, Yale University, P.O. Box 208106, New Haven, Connecticut 06520 USA The Malpighiaceae are a family of ;1250 species of predominantly New World tropical ¯owering plants. Infrafamilial classi®cation has long been based on fruit characters. Phylogenetic analyses of chloroplast DNA nucleotide sequences were analyzed to help resolve the phylogeny of Malpighiaceae. A total of 79 species, representing 58 of the 65 currently recognized genera, were studied. -
Antonio José Cavanilles (1745-1804)
ANTONIO JOSÉ CAVANILLES (1745-1804) Segundo centenario de la muerte de un gran botánico ANTONIO JOSÉ CAVANILLES (1745-1804) Segundo centenario de la muerte de un gran botánico Valencia Real Sociedad Económica de Amigos del País 2004 1. Dalia (cultivar de Dahlia pinnata Cav.). Según el sistema internacional de clasificación, pertenece al grupo “flor semicactus”. 2. Rosa (Rosa x centifolia L.). 3. Amapola (Papaver rhoeas L.). Variedad de flor doble. 4. Tulipán (variedad de jardín de Tulipa gesneriana L.) 5. Áster de China (Callistephus chinensis L.) = Nees (Aster chinensis L.), variedad de flor doble. 6. Jazmín oloroso (Jasminum odoratissimum L.). 7. Adormidera (Papaver somniferum L.). Variedad de jardín. 8. Crisantemo (Chysanthemum x indicum L.). 9. Clavel (Dianthus caryophyllus L.). 10. Perpetua (Helichrysum italicum (Roth) G. Don = Gnaphalium italicum Roth.). 11. Hortensia (Hydrangea macrophylla (Thunb.) (Ser. = Viburnum macrophyllum Thunb.) 12. Fucsia (Fuchsia fulgens DC.). Identificación y esquema por María José López Terrada. Edita: Real Sociedad Económica de Amigos del País Valencia, 2004 ISBN: 84-482-3874-5 Depósito legal: V. 4.381 - 2004 Artes Gráficas Soler, S. L. - La Olivereta, 28 - 46018 Valencia ÍNDICE Presentación de Francisco R. Oltra Climent. Director de la Real Socie- dad Económica de Amigos del País de Valencia ........................... 1 La obra de Cavanilles en la “Económica”, de Manuel Portolés i Sanz. Coordinador por la Real Sociedad Económica de Amigos del País de Valencia de “2004: año de Cavanilles” ...................................... 3 Botànic Cavanilles per sempre, de Francisco Tomás Vert. Rector de la Universitat de València ........................................................ 5 Palabras de Rafael Blasco Castany. Conseller de Territorio y Vivienda de la Generalitat Valenciana ..................................................... -
Flora Montiberica 28: 3-22 (XII-2004)
FLORA MONTIBERICA Publicación periódica especializada en trabajos sobre la flora del Sistema Ibérico Vol. 28 Valencia, XII-2004 FLORA MONTIBERICA Publicación independiente sobre temas relacionados con la flora de la Cordillera Ibérica (plantas vasculares). Edición en Internet: http://www.floramontiberica.org Editor y Redactor general: Gonzalo Mateo Sanz. Jardín Botánico. Universidad de Valencia. C/ Quart, 80. E-46008-Valencia. Redactores adjuntos: Cristina Torres Gómez y Javier Fabado Alós Comisión Asesora: Antoni Aguilella Palasí (Valencia) Juan A. Alejandre Sáenz (Vitoria) Vicente J. Arán Redó (Madrid) Manuel Benito Crespo Villalba (Alicante) José María de Jaime Lorén (Valencia) Emilio Laguna Lumbreras (Valencia) Pedro Montserrat Recoder (Jaca) Depósito Legal: V-5097-1995 ISSN: 1138-5952 Imprime: MOLINER-40 (GÓMEZ COLL, S.L.) Tel./Fax 390 3735 - Burjasot (Valencia). Portada: Phlomis crinita Cav., procedente dela cuesta de Barig (Valen- cia), localidad clásica cavanillesiana. Flora Montiberica 28: 3-22 (XII-2004) SOBRE LOS GÉNEROS DESCRITOS POR CAVANILLES. Emilio LAGUNA LUMBRERAS (1) Generalitat Valenciana. Conselleria de Territorio y Vivienda. Servicio de Conservación y Gestión de la Biodiversidad. Arquitecto Alfaro, 39. E-46011. Valencia. [email protected] ABSTRACT: A provisory list of vascular plant genera established by A. J. Cava- nilles is given. Cavanilles created at least 100 new genera, 54 of them being in current use. These genera have been used to generate the name of 2 orders, 10 families, 7 sub- families, 16 tribes and 9 subtribes; at least 1 order (Calycerales) and 5 families (Calyce- raceae, Cobaeaceae, Epacridaceae, Eucryphyaceae and Oleandraceae) are generally accepted and under current use. Most of these taxa belong to the tropical and subtropical flora. -
The Evolution of Bat Pollination: a Phylogenetic Perspective
Annals of Botany 104: 1017–1043, 2009 doi:10.1093/aob/mcp197, available online at www.aob.oxfordjournals.org INVITED REVIEW The evolution of bat pollination: a phylogenetic perspective Theodore H. Fleming1,*, Cullen Geiselman2 and W. John Kress3 1Emeritus, Department of Biology, University of Miami, Coral Gables, FL 33124, USA, 2Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458, USA and 3Department of Botany, MRC-166, National Museum of Natural History, Smithsonian Institution, PO Box 37012, Washington, DC 20013-7012, USA Received: 2 April 2009 Returned for revision: 27 May 2009 Accepted: 13 July 2009 Published electronically: 29 September 2009 † Background Most tropical and subtropical plants are biotically pollinated, and insects are the major pollinators. A small but ecologically and economically important group of plants classified in 28 orders, 67 families and about 528 species of angiosperms are pollinated by nectar-feeding bats. From a phylogenetic perspective this is a derived pollination mode involving a relatively large and energetically expensive pollinator. Here its ecologi- cal and evolutionary consequences are explored. Downloaded from † Scope and Conclusions This review summarizes adaptations in bats and plants that facilitate this interaction and discusses the evolution of bat pollination from a plant phylogenetic perspective. Two families of bats contain specialized flower visitors, one in the Old World and one in the New World. Adaptation to pollination by bats has evolved independently many times from a variety of ancestral conditions, including insect-, bird- and non-volant mammal-pollination. Bat pollination predominates in very few families but is relatively common in certain angiosperm subfamilies and tribes.