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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 -
Keene, Jeremy 11-21-13
A Reassessment of Monopyle (Gloxinieae:Gesneriaceae) A dissertation presented to the faculty of the College of Arts and Sciences of Ohio University In partial fulfillment of the requirements for the degree Doctor of Philosophy Jeremy L. Keene December 2013 © 2013 Jeremy L. Keene. All Rights Reserved. 2 This dissertation titled A Reassessment of Monopyle (Gloxinieae: Gesneriaceae) by JEREMY L. KEENE has been approved for the Department of Environmental and Plant Biology and the College of Arts and Sciences by Harvey E. Ballard, Jr. Associate Professor of Environmental and Plant Biology Robert Frank Dean, College of Arts and Sciences 3 ABSTRACT KEENE, JEREMY L., Ph.D., December 2013, Environmental and Plant Biology A Reassessment of Monopyle (Gloxinieae: Gesneriaceae) Director of Dissertation: Harvey E. Ballard, Jr. Monopyle Moritz ex Benth. is a genus of herbs or suffrutescent herbs distributed from Guatemala southward into northern South America. This assemblage of plants is characterized by the presence of anisophyllous leaves, uncinate trichomes, and campanulate flowers. The genus was last revised in 1945 by Conrad Morton. Since that time, few additional taxa have been recognized. It was comprised of 22 described species in 2011, with two infraspecific taxa. Also, there has been limited sampling of this genus for phylogenetic studies to assess the evolution of the genus. There were two primary foci of this research, a morphological characterization of the species within Monopyle and molecular analyses of the species within Monopyle and other closely related genera. A detailed morphological analysis was performed to determine the morphological differentiation between taxa. This analysis also confirmed which diagnostic characters identified in previous studies were valid and useful. -
Development of Leaf Shape and Vein Homologies in Five Species of the Genus Ipomoea (Convolvulaceae)
University of Northern Iowa UNI ScholarWorks Dissertations and Theses @ UNI Student Work 2014 Development of leaf shape and vein homologies in five species of the genus Ipomoea (Convolvulaceae) Austin William Jones University of Northern Iowa Let us know how access to this document benefits ouy Copyright ©2014 Austin William Jones Follow this and additional works at: https://scholarworks.uni.edu/etd Part of the Botany Commons, and the Plant Biology Commons Recommended Citation Jones, Austin William, "Development of leaf shape and vein homologies in five species of the genus Ipomoea (Convolvulaceae)" (2014). Dissertations and Theses @ UNI. 326. https://scholarworks.uni.edu/etd/326 This Open Access Thesis is brought to you for free and open access by the Student Work at UNI ScholarWorks. It has been accepted for inclusion in Dissertations and Theses @ UNI by an authorized administrator of UNI ScholarWorks. For more information, please contact [email protected]. Copyright by AUSTIN W. JONES 2014 All Rights Reserved DEVELOPMENT OF LEAF SHAPE AND VEIN HOMOLOGIES IN FIVE SPECIES OF THE GENUS IPOMOEA (CONVOLVULACEAE) An Abstract of a Thesis Submitted in Partial Fulfillment of the Requirements for the Degree Master of Science Austin William Jones University of Northern Iowa May 2014 ABSTRACT Angiosperm leaves are extremely variable in form while predominantly maintaining the function of the primary photosynthetic organ of the plant. Changes in leaf form can result from myriad physiological processes which may be influenced by ecology, physical stimuli, phylogeny, or other factors. In studying the development of divergent leaf forms among closely related species, conserved morphological elements may be identified that are not apparent in the mature form. -
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. -
Towards Resolving Lamiales Relationships
Schäferhoff et al. BMC Evolutionary Biology 2010, 10:352 http://www.biomedcentral.com/1471-2148/10/352 RESEARCH ARTICLE Open Access Towards resolving Lamiales relationships: insights from rapidly evolving chloroplast sequences Bastian Schäferhoff1*, Andreas Fleischmann2, Eberhard Fischer3, Dirk C Albach4, Thomas Borsch5, Günther Heubl2, Kai F Müller1 Abstract Background: In the large angiosperm order Lamiales, a diverse array of highly specialized life strategies such as carnivory, parasitism, epiphytism, and desiccation tolerance occur, and some lineages possess drastically accelerated DNA substitutional rates or miniaturized genomes. However, understanding the evolution of these phenomena in the order, and clarifying borders of and relationships among lamialean families, has been hindered by largely unresolved trees in the past. Results: Our analysis of the rapidly evolving trnK/matK, trnL-F and rps16 chloroplast regions enabled us to infer more precise phylogenetic hypotheses for the Lamiales. Relationships among the nine first-branching families in the Lamiales tree are now resolved with very strong support. Subsequent to Plocospermataceae, a clade consisting of Carlemanniaceae plus Oleaceae branches, followed by Tetrachondraceae and a newly inferred clade composed of Gesneriaceae plus Calceolariaceae, which is also supported by morphological characters. Plantaginaceae (incl. Gratioleae) and Scrophulariaceae are well separated in the backbone grade; Lamiaceae and Verbenaceae appear in distant clades, while the recently described Linderniaceae are confirmed to be monophyletic and in an isolated position. Conclusions: Confidence about deep nodes of the Lamiales tree is an important step towards understanding the evolutionary diversification of a major clade of flowering plants. The degree of resolution obtained here now provides a first opportunity to discuss the evolution of morphological and biochemical traits in Lamiales. -
Collections Policy
Chicago Botanic Garden COLLECTIONS POLICY 1 Collections Policy July 2018 2 COLLECTIONS POLICY TABLE OF CONTENTS Mission Statement ................................................................................................................... 1 Intent of Collections Policy Document ..................................................................................... 1 Purpose of Collections .............................................................................................................. 1 Scope of Collections ................................................................................................................. 1 1) Display Plant Collections .......................................................................................... 2 Seasonal Display Collections ........................................................................... 2 Permanent Display Gardens ............................................................................ 2 Aquatic Garden ................................................................................... 2 Bonsai Collection ................................................................................. 3 Graham Bulb Garden .......................................................................... 3 Grunsfeld Children’s Growing Garden ................................................. 3 Circle Garden ....................................................................................... 3 Kleinman Family Cove ........................................................................ -
Downloaded and Combined with Our Assemblies 178 ( Serrano-Serrano Et Al
bioRxiv preprint doi: https://doi.org/10.1101/817221; this version posted February 13, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 2 Co-expression clustering across flower development 3 identifies modules for diverse floral forms in 4 Achimenes (Gesneriaceae) 5 6 Wade R Roberts1,2, Eric H Roalson1 7 8 1 School of Biological Sciences, Washington State University, Pullman, WA, United States 9 2 Current address: Biological Sciences, University of Arkansas, Fayetteville, AR, United States 10 11 Corresponding Author: 12 Wade Roberts1 13 Biological Sciences, University of Arkansas, SCEN 601, Fayetteville, AR, 72701, United States 14 Email address: [email protected] 15 16 Abstract 17 Background. Genetic pathways involved with flower color and shape are thought to play an 18 important role in the development of flowers associated with different pollination syndromes, 19 such as those associated with bee, butterfly, or hummingbird pollination. Because pollination 20 syndromes are complex traits that are orchestrated by multiple genes and pathways, the gene 21 networks have not been explored. Gene co-expression networks provide a systems level 22 approach to identify important contributors to floral diversification. 23 Methods. RNA-sequencing was used to assay gene expression across two stages of flower 24 development (an early bud and an intermediate stage) in 10 species of Achimenes 25 (Gesneriaceae). Two stage-specific co-expression networks were created from 9503 orthologs 26 and analyzed to identify module hubs and the network periphery. -
Trends in Flower Symmetry Evolution Revealed Through Phylogenetic and Developmental Genetic Advances
Trends in flower symmetry evolution revealed through phylogenetic and developmental genetic advances Lena C. Hileman rstb.royalsocietypublishing.org Ecology and Evolutionary Biology, University of Kansas, 1200 Sunnyside Avenue, Lawrence, KS 66045, USA A striking aspect of flowering plant (angiosperm) diversity is variation in flower symmetry. From an ancestral form of radial symmetry (polysymmetry, actinomorphy), multiple evolutionary transitions have contributed to instan- Review ces of non-radial forms, including bilateral symmetry (monosymmetry, zygomorphy) and asymmetry. Advances in flowering plant molecular Cite this article: Hileman LC. 2014 Trends in phylogenetic research and studies of character evolution as well as detailed flower symmetry evolution revealed through flower developmental genetic studies in a few model species (e.g. Antirrhinum phylogenetic and developmental genetic majus, snapdragon) have provided a foundation for deep insights into flower symmetry evolution. From phylogenetic studies, we have a better under- advances. Phil. Trans. R. Soc. B 369: 20130348. standing of where during flowering plant diversification transitions from http://dx.doi.org/10.1098/rstb.2013.0348 radial to bilateral flower symmetry (and back to radial symmetry) have occurred. From developmental studies, we know that a genetic programme One contribution of 14 to a Theme Issue largely dependent on the functional action of the CYCLOIDEA gene is necess- ‘Contemporary and future studies in plant ary for differentiation along the snapdragon dorsoventral flower axis. Bringing these two lines of inquiry together has provided surprising insights into both speciation, morphological/floral evolution the parallel recruitment of a CYC-dependent developmental programme and polyploidy: honouring the scientific during independent transitions to bilateral flower symmetry, and the modifi- contributions of Leslie D. -
Why Continue with Floristic Checklists in Mexico
Botanical Sciences 97 (4): 741-753. 2019 Received: February 15, 2019, accepted: July 15, 2019 DOI: 10.17129/botsci.2174 On line first: December 17, 2019 Taxonomy and Floristics/Taxonomía y Florística Why continue with floristic checklists in Mexico? The case of the Tacaná- Boquerón Priority Terrestrial Region, in the Mexican State of Chiapas ¿Por qué continuar realizando listados florísticos en México? El caso de la Región Terrestre Prioritaria Tacaná-Boquerón, Chiapas Rubén Martínez-Camilo1*, Nayely Martínez-Meléndez2, Manuel Martínez-Meléndez3,4, Miguel Ángel Pérez- Farrera3, and Derio Antonio Jiménez-López1 1 Centro del Cambio Global y La Sustentabilidad A.C., Villahermosa, Tabasco, México. 2 El Colegio de la Frontera Sur, San Cristóbal de Las Casas, Chiapas, México. 3 Herbario Eizi Matuda; Laboratorio de Ecología Evolutiva, Instituto de Ciencias Biológicas, Universidad de Ciencias y Artes de Chiapas, Tuxtla Gutiérrez, Chiapas, México. 4 Eizia A.C., Tuxtla Gutiérrez, Chiapas, México. * Corresponding author: [email protected] Abstract Background: Some regions of Mexico have been relatively well explored floristically and estimates of the vascular plant richness they contain have been obtained. However, there are still regions that require effort to obtain the most appropriate lists of flora possible that consider both systemization of the information and that benefit from recent botanical explorations. Questions: What is the species richness of vascular plants in the Tacaná-Boquerón Priority Terrestrial Region? What proportion of the species are endemic or included in risk categories? Study sites and dates: Tacaná-Boquerón Priority Terrestrial Region, Chiapas State, Mexico. This region is on the Guatemala border and covers an area of 57,400 ha. -
Lamiales – Synoptical Classification Vers
Lamiales – Synoptical classification vers. 2.6.2 (in prog.) Updated: 12 April, 2016 A Synoptical Classification of the Lamiales Version 2.6.2 (This is a working document) Compiled by Richard Olmstead With the help of: D. Albach, P. Beardsley, D. Bedigian, B. Bremer, P. Cantino, J. Chau, J. L. Clark, B. Drew, P. Garnock- Jones, S. Grose (Heydler), R. Harley, H.-D. Ihlenfeldt, B. Li, L. Lohmann, S. Mathews, L. McDade, K. Müller, E. Norman, N. O’Leary, B. Oxelman, J. Reveal, R. Scotland, J. Smith, D. Tank, E. Tripp, S. Wagstaff, E. Wallander, A. Weber, A. Wolfe, A. Wortley, N. Young, M. Zjhra, and many others [estimated 25 families, 1041 genera, and ca. 21,878 species in Lamiales] The goal of this project is to produce a working infraordinal classification of the Lamiales to genus with information on distribution and species richness. All recognized taxa will be clades; adherence to Linnaean ranks is optional. Synonymy is very incomplete (comprehensive synonymy is not a goal of the project, but could be incorporated). Although I anticipate producing a publishable version of this classification at a future date, my near- term goal is to produce a web-accessible version, which will be available to the public and which will be updated regularly through input from systematists familiar with taxa within the Lamiales. For further information on the project and to provide information for future versions, please contact R. Olmstead via email at [email protected], or by regular mail at: Department of Biology, Box 355325, University of Washington, Seattle WA 98195, USA. -
Botany-Illustrated-J.-Glimn-Lacy-P.-Kaufman-Springer-2006.Pdf
Janice Glimn-Lacy Peter B. Kaufman 6810 Shadow Brook Court Department of Molecular, Cellular, and Indianapolis, IN 46214-1901 Developmental Biology USA University of Michigan [email protected] Ann Arbor, MI 48109-1048 USA [email protected] Library of Congress Control Number: 2005935289 ISBN-10: 0-387-28870-8 eISBN: 0-387-28875-9 ISBN-13: 978-0387-28870-3 Printed on acid-free paper. C 2006 Janice Glimn-Lacy and Peter B. Kaufman All rights reserved. This work may not be translated or copied in whole or in part without the written permission of the publisher (Springer Science+Business Media, Inc., 233 Spring Street, New York, NY 10013, USA), except for brief excerpts in connection with reviews or scholarly analysis. Use in connection with any form of information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed is forbidden. The use in this publication of trade names, trademarks, service marks, and similar terms, even if they are not identified as such, is not to be taken as an expression of opinion as to whether or not they are subject to proprietary rights. Printed in the United States of America. (TB/MVY) 987654321 springer.com Preface This is a discovery book about plants. It is for everyone For those interested in the methods used and the interested in plants including high school and college/ sources of plant materials in the illustrations, an expla- university students, artists and scientific illustrators, nation follows. For a developmental series of drawings, senior citizens, wildlife biologists, ecologists, profes- there are several methods. -
Chapter 4 Phytomorph and Geomorph Identification ©
1 Chapter 4 Phytomorph and Geomorph Identification © This Chapter is based on three published works: (1) a paper by Hugh O Neall (1944) that identifies two New World plants (sunflower and chili peppers) in the Voynich manuscript; (2) a paper of Tucker and Talbert (2013) which identified 39 plants in the Voynich as indigenous to the New World; (3) a paper by Tucker and Janick (2016) which extended the list to 59 species. Although many of the illustrations of the Voynich Codex on first blush could be considered bizarre or whimsical (See Figure in Chapter 14) most contain morphological structures which permit botanical identification. Many enthusiasts have attempted to analyze the plants of the Voynich Codex, but few are knowledgeable plant taxonomists or botanists, despite their large web presence. Most of the plant identification has been predicated on the conclusion that the Voynich is a 15th century European manuscript (Friedman 1962). The principal reports in a web report by non botanists Edith and Erica Sherwood (http:www.edithsherwood.comn/coyhnich_botanical_plants) who identifies he plants as Mediterranean based on their premise that Voynich is a 15th century Italian manuscript and claims to find signature of Leonardo da Vinci in voynich drawings. We respectfully disagree with both assertions. The first exception to the conclusion that the Voynich plants were European is a short remarkable 1944 paper in Speculum (a refereed journal of the Medieval Academy of America) by the distinguished plant taxonomist, the Rev./Dr. Hugh O’Neill (1894–1969), former Director of the Herbarium (official acronym LCU) at the Catholic University of America (CUA) in Washington, D.C.