Index of Flowering Plants
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MISSOURI BOTANICAL GARDEN RESEARCHER DISCOVERS NEW GENUS Finding New Genus Rare in Modern Plant Taxonomy
Date: October 15, 2010 MISSOURI BOTANICAL GARDEN RESEARCHER DISCOVERS NEW GENUS Finding New Genus Rare in Modern Plant Taxonomy (ST. LOUIS): An article published in the October issue of the Annals of the Missouri Botanical Garden describes a new genus of tree of the Aptandraceae family, a group that is related to the sandalwoods (order Santalales). The genus, which has been given the name Hondurodendron , is endemic to Honduras and means “tree of Honduras.” In the article, “Hondurodendron, a New Monotypic Genus of Aptandraceae from Honduras,” lead author Dr. Carmen Ulloa, associate curator at the Missouri Botanical Garden, and co-authors Dr. Daniel L. Nickrent, Southern Illinois University-Carbondale, Dr. Caroline Whitefoord, The Natural History Museum in London, and Dr. Daniel L. Kelly, Trinity College in Dublin, describe the genus as a tree about 40-feet-tall, with minute male and female flowers less than 2 mm (1/8 inch) wide, borne respectively on separate plants. The tiny stamens have rather unusual anthers opening by three valves. The fruit measures 2 cm (1 inch) across; it is tightly wrapped by the calyx which enlarges greatly as the fruit matures and eventually may even project beyond as a flared limb. The authors named the single species known of this genus as Hondurodendron urceolatum with the Latin specific epithet meaning “shaped like a pitcher or urn” because of the striking form of the fruit. The first specimens of this genus were collected by Kelly and a team of researchers and students during a plot-based survey of the forest vegetation of Parque Nacional El Cusuco in northwest Honduras in 2004 and 2006. -
"Santalales (Including Mistletoes)"
Santalales (Including Introductory article Mistletoes) Article Contents . Introduction Daniel L Nickrent, Southern Illinois University, Carbondale, Illinois, USA . Taxonomy and Phylogenetics . Morphology, Life Cycle and Ecology . Biogeography of Mistletoes . Importance of Mistletoes Online posting date: 15th March 2011 Mistletoes are flowering plants in the sandalwood order that produce some of their own sugars via photosynthesis (Santalales) that parasitise tree branches. They evolved to holoparasites that do not photosynthesise. Holopar- five separate times in the order and are today represented asites are thus totally dependent on their host plant for by 88 genera and nearly 1600 species. Loranthaceae nutrients. Up until recently, all members of Santalales were considered hemiparasites. Molecular phylogenetic ana- (c. 1000 species) and Viscaceae (550 species) have the lyses have shown that the holoparasite family Balano- highest species diversity. In South America Misodendrum phoraceae is part of this order (Nickrent et al., 2005; (a parasite of Nothofagus) is the first to have evolved Barkman et al., 2007), however, its relationship to other the mistletoe habit ca. 80 million years ago. The family families is yet to be determined. See also: Nutrient Amphorogynaceae is of interest because some of its Acquisition, Assimilation and Utilization; Parasitism: the members are transitional between root and stem para- Variety of Parasites sites. Many mistletoes have developed mutualistic rela- The sandalwood order is of interest from the standpoint tionships with birds that act as both pollinators and seed of the evolution of parasitism because three early diverging dispersers. Although some mistletoes are serious patho- families (comprising 12 genera and 58 species) are auto- gens of forest and commercial trees (e.g. -
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, -
Well-Known Plants in Each Angiosperm Order
Well-known plants in each angiosperm order This list is generally from least evolved (most ancient) to most evolved (most modern). (I’m not sure if this applies for Eudicots; I’m listing them in the same order as APG II.) The first few plants are mostly primitive pond and aquarium plants. Next is Illicium (anise tree) from Austrobaileyales, then the magnoliids (Canellales thru Piperales), then monocots (Acorales through Zingiberales), and finally eudicots (Buxales through Dipsacales). The plants before the eudicots in this list are considered basal angiosperms. This list focuses only on angiosperms and does not look at earlier plants such as mosses, ferns, and conifers. Basal angiosperms – mostly aquatic plants Unplaced in order, placed in Amborellaceae family • Amborella trichopoda – one of the most ancient flowering plants Unplaced in order, placed in Nymphaeaceae family • Water lily • Cabomba (fanwort) • Brasenia (watershield) Ceratophyllales • Hornwort Austrobaileyales • Illicium (anise tree, star anise) Basal angiosperms - magnoliids Canellales • Drimys (winter's bark) • Tasmanian pepper Laurales • Bay laurel • Cinnamon • Avocado • Sassafras • Camphor tree • Calycanthus (sweetshrub, spicebush) • Lindera (spicebush, Benjamin bush) Magnoliales • Custard-apple • Pawpaw • guanábana (soursop) • Sugar-apple or sweetsop • Cherimoya • Magnolia • Tuliptree • Michelia • Nutmeg • Clove Piperales • Black pepper • Kava • Lizard’s tail • Aristolochia (birthwort, pipevine, Dutchman's pipe) • Asarum (wild ginger) Basal angiosperms - monocots Acorales -
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 -
503 Flora V7 2.Doc 3
Browse LNG Precinct ©WOODSIDE Browse Liquefied Natural Gas Precinct Strategic Assessment Report (Draft for Public Review) December 2010 Appendix C-18 A Vegetation and Flora Survey of James Price Point: Wet Season 2009 A Vegetation and Flora Survey of James Price Point: Wet Season 2009 Prepared for Department of State Development December 2009 A Vegetation and Flora Survey of James Price Point: Wet Season 2009 © Biota Environmental Sciences Pty Ltd 2009 ABN 49 092 687 119 Level 1, 228 Carr Place Leederville Western Australia 6007 Ph: (08) 9328 1900 Fax: (08) 9328 6138 Project No.: 503 Prepared by: P. Chukowry, M. Maier Checked by: G. Humphreys Approved for Issue: M. Maier This document has been prepared to the requirements of the client identified on the cover page and no representation is made to any third party. It may be cited for the purposes of scientific research or other fair use, but it may not be reproduced or distributed to any third party by any physical or electronic means without the express permission of the client for whom it was prepared or Biota Environmental Sciences Pty Ltd. This report has been designed for double-sided printing. Hard copies supplied by Biota are printed on recycled paper. Cube:Current:503 (Kimberley Hub Wet Season):Doc:Flora:503 flora v7_2.doc 3 A Vegetation and Flora Survey of James Price Point: Wet Season 2009 4 Cube:Current:503 (Kimberley Hub Wet Season):Doc:Flora:503 flora v7_2.doc Biota A Vegetation and Flora Survey of James Price Point: Wet Season 2009 A Vegetation and Flora Survey of James Price -
Two New Genera in the Omphalodes Group (Cynoglosseae, Boraginaceae)
Nova Acta Científica Compostelana (Bioloxía),23 : 1-14 (2016) - ISSN 1130-9717 ARTÍCULO DE INVESTIGACIÓN Two new genera in the Omphalodes group (Cynoglosseae, Boraginaceae) Dous novos xéneros no grupo Omphalodes (Cynoglosseae, Boraginaceae) M. SERRANO1, R. CARBAJAL1, A. PEREIRA COUTINHO2, S. ORTIZ1 1 Department of Botany, Faculty of Pharmacy, University of Santiago de Compostela, 15782 Santiago de Compostela , Spain 2 CFE, Centre for Functional Ecology, Department of Life Sciences, University of Coimbra, 3000-456 Coimbra, Portugal *[email protected]; [email protected]; [email protected]; [email protected] *: Corresponding author (Recibido: 08/06/2015; Aceptado: 01/02/2016; Publicado on-line: 04/02/2016) Abstract Omphalodes (Boraginaceae, Cynoglosseae) molecular phylogenetic relationships are surveyed in the context of the tribe Cynoglosseae, being confirmed that genusOmphalodes is paraphyletic. Our work is focused both in the internal relationships among representatives of Omphalodes main subgroups (and including Omphalodes verna, the type species), and their relationships with other Cynoglosseae genera that have been related to the Omphalodes group. Our phylogenetic analysis of ITS and trnL-trnF molecular markers establish close relationships of the American Omphalodes with the genus Mimophytum, and also with Cynoglossum paniculatum and Myosotidium hortensia. The southwestern European annual Omphalodes species form a discrete group deserving taxonomic recognition. We describe two new genera to reduce the paraphyly in the genus Omphalodes, accommodating the European annual species in Iberodes and Cynoglossum paniculatum in Mapuchea. The pollen of the former taxon is described in detail for the first time. Keywords: Madrean-Tethyan, phylogeny, pollen, systematics, taxonomy Resumo Neste estudo analisamos as relacións filoxenéticas deOmphalodes (Boraginaceae, Cynoglosseae) no contexto da tribo Cynoglosseae, confirmándose como parafilético o xéneroOmphalodes . -
December 2012 Number 1
Calochortiana December 2012 Number 1 December 2012 Number 1 CONTENTS Proceedings of the Fifth South- western Rare and Endangered Plant Conference Calochortiana, a new publication of the Utah Native Plant Society . 3 The Fifth Southwestern Rare and En- dangered Plant Conference, Salt Lake City, Utah, March 2009 . 3 Abstracts of presentations and posters not submitted for the proceedings . 4 Southwestern cienegas: Rare habitats for endangered wetland plants. Robert Sivinski . 17 A new look at ranking plant rarity for conservation purposes, with an em- phasis on the flora of the American Southwest. John R. Spence . 25 The contribution of Cedar Breaks Na- tional Monument to the conservation of vascular plant diversity in Utah. Walter Fertig and Douglas N. Rey- nolds . 35 Studying the seed bank dynamics of rare plants. Susan Meyer . 46 East meets west: Rare desert Alliums in Arizona. John L. Anderson . 56 Calochortus nuttallii (Sego lily), Spatial patterns of endemic plant spe- state flower of Utah. By Kaye cies of the Colorado Plateau. Crystal Thorne. Krause . 63 Continued on page 2 Copyright 2012 Utah Native Plant Society. All Rights Reserved. Utah Native Plant Society Utah Native Plant Society, PO Box 520041, Salt Lake Copyright 2012 Utah Native Plant Society. All Rights City, Utah, 84152-0041. www.unps.org Reserved. Calochortiana is a publication of the Utah Native Plant Society, a 501(c)(3) not-for-profit organi- Editor: Walter Fertig ([email protected]), zation dedicated to conserving and promoting steward- Editorial Committee: Walter Fertig, Mindy Wheeler, ship of our native plants. Leila Shultz, and Susan Meyer CONTENTS, continued Biogeography of rare plants of the Ash Meadows National Wildlife Refuge, Nevada. -
Table of Contents Below) with Family Name Provided
1 Australian Plants Society Plant Table Profiles – Sutherland Group (updated August 2021) Below is a progressive list of all cultivated plants from members’ gardens and Joseph Banks Native Plants Reserve that have made an appearance on the Plant Table at Sutherland Group meetings. Links to websites are provided for the plants so that further research can be done. Plants are grouped in the categories of: Trees and large shrubs (woody plants generally taller than 4 m) Medium to small shrubs (woody plants from 0.1 to 4 m) Ground covers or ground-dwelling (Grasses, orchids, herbaceous and soft-wooded plants, ferns etc), as well as epiphytes (eg: Platycerium) Vines and scramblers Plants are in alphabetical order by botanic names within plants categories (see table of contents below) with family name provided. Common names are included where there is a known common name for the plant: Table of Contents Trees and Large shrubs........................................................................................................................... 2 Medium to small shrubs ...................................................................................................................... 23 Groundcovers and other ground‐dwelling plants as well as epiphytes. ............................................ 64 Vines and Scramblers ........................................................................................................................... 86 Sutherland Group http://sutherland.austplants.com.au 2 Trees and Large shrubs Acacia decurrens -
Medicinal Plants in the High Mountains of Northern Jordan
Vol. 6(6), pp. 436-443, June 2014 DOI: 10.5897/IJBC2014.0713 Article Number: 28D56BF45309 ISSN 2141-243X International Journal of Biodiversity Copyright © 2014 Author(s) retain the copyright of this article and Conservation http://www.academicjournals.org/IJBC Full Length Research Paper Medicinal plants in the high mountains of northern Jordan Sawsan A. Oran and Dawud M. Al- Eisawi Department of Biological Sciences, Faculty of Sciences, University of Jordan, Amman, Jordan. Receive 10 April, 2014; Accepted 24 April, 2014 The status of medicinal plants in the high mountains of northern Jordan was evaluated. A total of 227 plant species belonging to 54 genera and 60 families were recorded. The survey is based on field trips conducted in the areas that include Salt, Jarash, Balka, Amman and Irbid governorates. Line transect method was used; collection of plant species was done and voucher specimens were deposited. A map for the target area was provided; the location of the study area grids in relation to their governorate was included. Key words: Medicinal plants, high mountains of northern Jordan, folk medicine. INTRODUCTION Human beings have always made use of their native cinal plant out of 670 flowering plant species identified in flora, not just as a source of nutrition, but also for fuel, the same area in Jordan. Recent studies are published medicines, clothing, dwelling and chemical production. on the status of medicinal plants that are used fofolk Traditional knowledge of plants and their properties has medicine by the local societies (Oran, 2014). always been transmitted from generation to generation Medicinal plants in Jordan represent 20% of the total through the natural course of everyday life (Kargıoğlu et flora (Oran et al., 1998). -
Wingnut (Juglandaceae)
83 Wingnut (Juglandaceae) as a new generic host for Pityophthorus juglandis (Coleoptera: Curculionidae) and the thousand cankers disease pathogen, Geosmithia morbida (Ascomycota: Hypocreales) Stacy M. Hishinuma, Paul L. Dallara, Mohammad A. Yaghmour, Marcelo M. Zerillo, Corwin M. Parker, Tatiana V. Roubtsova, Tivonne L. Nguyen, Ned A. Tisserat, Richard M. Bostock, Mary L. Flint, Steven J. Seybold1 Abstract—The walnut twig beetle (WTB), Pityophthorus juglandis Blackman (Coleoptera: Curculionidae), vectors a fungus, Geosmithia morbida Kolařík, Freeland, Utley, and Tisserat (Ascomycota: Hypocreales), which colonises and kills the phloem of walnut and butternut trees, Juglans Linnaeus (Juglandaceae). Over the past two decades, this condition, known as thousand cankers disease (TCD), has led to the widespread mortality of Juglans species in the United States of America. Recently the beetle and pathogen were discovered on several Juglans species in northern Italy. Little is known about the extra-generic extent of host acceptability and suitability for the WTB. We report the occurrence of both the WTB and G. morbida in three species of wingnut, Pterocarya fraxinifolia Spach, Pterocarya rhoifolia Siebold and Zuccarini, and Pterocarya stenoptera de Candolle (Juglandaceae) growing in the United States Department of Agriculture-Agricultural Research Service, National Clonal Germplasm Repository collection in northern California (NCGR) and in the Los Angeles County Arboretum and Botanic Garden in southern California, United States of America. In two instances (once in P. stenoptera and once in P. fraxinifolia) teneral (i.e., brood) adult WTB emerged and were collected more than four months after infested branch sections had been collected in the field. Koch’s postulates were satisfied with an isolate of G. -
Inflorescence Dimorphism, Heterodichogamy and Thrips
Annals of Botany 113: 467–476, 2014 doi:10.1093/aob/mct278, available online at www.aob.oxfordjournals.org Inflorescence dimorphism, heterodichogamy and thrips pollination in Platycarya strobilacea (Juglandaceae) Tatsundo Fukuhara* and Shin-ichiro Tokumaru Faculty of Education, Fukuoka University of Education, 1-1 Akama-Bunkyo-machi, Munakata, Fukuoka, Japan * For correspondence. E-mail [email protected] Received: 22 July 2013 Returned for revision: 11 September 2013 Accepted: 14 October 2013 Published electronically: 3 December 2013 † Background and Aims Unlike other taxa in Juglandaceae or in closely related families, which are anemophilous, Platycarya strobilacea has been suggested to be entomophilous. In Juglandaceae, Juglans and Carya show hetero- dichogamy, a reproductive strategy in which two morphs coexist in a population and undergo synchronous reciprocal sex changes. However, there has been no study focusing on heterodichogamy in the other six or seven genera, includ- ing Platycarya. † Methods Inflorescence architecture, sexual expression and pollination biology were examined in a P. strobilacea population in Japan. Flowering phenology was monitored daily for 24 trees in 2008 and 27 in 2009. Flower visitors and inhabitants were recorded or collected from different sexes and stages. † Key results The population of P. strobilacea showed heterodichogamous phenology with protogynous and duodi- chogamous–protandrous morphs. This dimorphism in dichogamy was associated with distinct inflorescence morph- ologies.Thrips pollination was suggested bythe frequent presence of thrips withattached pollen grains,the scarcityof other insect visitors, the synchronicity of thrips number in male spikes with the maturation of female flowers, and morphological characters shared with previously reported thrips-pollinated plants. Male spikes went through two consecutive stages: bright yellow and strong-scented M1 stage, and brownish and little-scented M2 stage.