New York Non-Native Plant Invasiveness Ranking Form
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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 -
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 -
(Callitrichaceae), a New Species from Java, Indonesia
Floribunda 2(3) 2003 57 CALLITRICHE NANA (CALLITRICHACEAE), A NEW SPECIES FROM JAVA, INDONESIA W.J.J.O. De Wilde, B.E.E. Duyfjes, B. Gravendeel, R.W.J.M. Van der Ham Nationaal Herbarium Nederland, Universiteit Leiden Branch, P.O. Box 9514, 2300 RA Leiden, The Netherlands B.C. Ho National University of Singapore, 10 Kent Ridge Crescent, Singapore Rugayah Herbarium Bogoriense, Pusat Penelitian Biologi–LIPI, Bogor, Indonesia G.T.P. Vo University of Natural Sciences–Hochiminh City, 227 Nguyen Van Cu St., Dist.5, Hochiminh City, Vietnam W.J.J.O. De Wilde, B.E.E. Duyfjes, B. Gravendeel, R.W.J.M. Van der Ham, B.C. Ho, Rugayah, G.T.P. Vo. 2003. Callitriche nana (Callitrichaceae), jenis baru dari Jawa, Indonesia. Floribunda 2(3): 57–66. –– Callitriche nana (Callitrichaceae) B.C. Ho & G.T.P Vo merupakan jenis Callitriche pertama yang ditemukan di Jawa. Jenis ini adalah tumbuhan terestrial. Di antara 50 jenis yang ada di dunia, Callitriche yang ditemukan di Jawa mempunyai ukuran paling kecil dan mempunyai karakter morfologi yang berbeda sekali dengan jenis lainnya. Analisis filogeni dengan menggunakan urutan rbcl menunjukkan bahwa Callitriche nana menduduki posisi yang terpisah dalam genus Callitriche. Kata kunci: Callitriche nana, Callitrichaceae, Indonesia, Jawa, filogeni. W.J.J.O. De Wilde, B.E.E. Duyfjes, B. Gravendeel, R.W.J.M. Van der Ham, B.C. Ho, Rugayah, G.T.P. Vo. 2003. Callitriche nana (Callitrichaceae), a new species from Java, Indonesia. Floribunda 2(3): 57–66. –– Callitriche nana B.C. Ho & G.T.P. Vo, the first Callitriche species from Java, is described. -
Introduction to Common Native & Invasive Freshwater Plants in Alaska
Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska Cover photographs by (top to bottom, left to right): Tara Chestnut/Hannah E. Anderson, Jamie Fenneman, Vanessa Morgan, Dana Visalli, Jamie Fenneman, Lynda K. Moore and Denny Lassuy. Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska This document is based on An Aquatic Plant Identification Manual for Washington’s Freshwater Plants, which was modified with permission from the Washington State Department of Ecology, by the Center for Lakes and Reservoirs at Portland State University for Alaska Department of Fish and Game US Fish & Wildlife Service - Coastal Program US Fish & Wildlife Service - Aquatic Invasive Species Program December 2009 TABLE OF CONTENTS TABLE OF CONTENTS Acknowledgments ............................................................................ x Introduction Overview ............................................................................. xvi How to Use This Manual .................................................... xvi Categories of Special Interest Imperiled, Rare and Uncommon Aquatic Species ..................... xx Indigenous Peoples Use of Aquatic Plants .............................. xxi Invasive Aquatic Plants Impacts ................................................................................. xxi Vectors ................................................................................. xxii Prevention Tips .................................................... xxii Early Detection and Reporting -
Alien Flora of Europe: Species Diversity, Temporal Trends, Geographical Patterns and Research Needs
Preslia 80: 101–149, 2008 101 Alien flora of Europe: species diversity, temporal trends, geographical patterns and research needs Zavlečená flóra Evropy: druhová diverzita, časové trendy, zákonitosti geografického rozšíření a oblasti budoucího výzkumu Philip W. L a m b d o n1,2#, Petr P y š e k3,4*, Corina B a s n o u5, Martin H e j d a3,4, Margari- taArianoutsou6, Franz E s s l7, Vojtěch J a r o š í k4,3, Jan P e r g l3, Marten W i n t e r8, Paulina A n a s t a s i u9, Pavlos A n d r i opoulos6, Ioannis B a z o s6, Giuseppe Brundu10, Laura C e l e s t i - G r a p o w11, Philippe C h a s s o t12, Pinelopi D e l i p e t - rou13, Melanie J o s e f s s o n14, Salit K a r k15, Stefan K l o t z8, Yannis K o k k o r i s6, Ingolf K ü h n8, Hélia M a r c h a n t e16, Irena P e r g l o v á3, Joan P i n o5, Montserrat Vilà17, Andreas Z i k o s6, David R o y1 & Philip E. H u l m e18 1Centre for Ecology and Hydrology, Hill of Brathens, Banchory, Aberdeenshire AB31 4BW, Scotland, e-mail; [email protected], [email protected]; 2Kew Herbarium, Royal Botanic Gardens Kew, Richmond, Surrey, TW9 3AB, United Kingdom; 3Institute of Bot- any, Academy of Sciences of the Czech Republic, CZ-252 43 Průhonice, Czech Republic, e-mail: [email protected], [email protected], [email protected], [email protected]; 4Department of Ecology, Faculty of Science, Charles University, Viničná 7, CZ-128 01 Praha 2, Czech Republic; e-mail: [email protected]; 5Center for Ecological Research and Forestry Applications, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain, e-mail: [email protected], [email protected]; 6University of Athens, Faculty of Biology, Department of Ecology & Systematics, 15784 Athens, Greece, e-mail: [email protected], [email protected], [email protected], [email protected], [email protected]; 7Federal Environment Agency, Department of Nature Conservation, Spittelauer Lände 5, 1090 Vienna, Austria, e-mail: [email protected]; 8Helmholtz Centre for Environmental Research – UFZ, Department of Community Ecology, Theodor-Lieser- Str. -
Systematics of Gratiola (Plantaginaceae)
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Doctoral Dissertations Graduate School 5-2008 Systematics of Gratiola (Plantaginaceae) Larry D. Estes University of Tennessee - Knoxville Follow this and additional works at: https://trace.tennessee.edu/utk_graddiss Part of the Ecology and Evolutionary Biology Commons Recommended Citation Estes, Larry D., "Systematics of Gratiola (Plantaginaceae). " PhD diss., University of Tennessee, 2008. https://trace.tennessee.edu/utk_graddiss/381 This Dissertation is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a dissertation written by Larry D. Estes entitled "Systematics of Gratiola (Plantaginaceae)." I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Doctor of Philosophy, with a major in Ecology and Evolutionary Biology. Randall L. Small, Major Professor We have read this dissertation and recommend its acceptance: Edward E. Schilling, Karen W. Hughes, Sally P. Horn Accepted for the Council: Carolyn R. Hodges Vice Provost and Dean of the Graduate School (Original signatures are on file with official studentecor r ds.) To the Graduate Council: I am submitting herewith a dissertation written by Larry Dwayne Estes entitled “Systematics of Gratiola (Plantaginaceae).” I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the requirements for the degree of Doctor of Philosophy, with a major in Ecology and Evolution. -
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. -
An Illustrated Key to the Alberta Figworts & Allies
AN ILLUSTRATED KEY TO THE ALBERTA FIGWORTS & ALLIES OROBANCHACEAE PHRYMACEAE PLANTAGINACEAE SCROPHULARIACEAE Compiled and writen by Lorna Allen & Linda Kershaw April 2019 © Linda J. Kershaw & Lorna Allen Key to Figwort and Allies Families In the past few years, the families Orobanchaceae, Plantaginaceae and Scrophulariaceae have under- gone some major revision and reorganization. Most of the species in the Scrophulariaceae in the Flora of Alberta (1983) are now in the Orobanchaceae and Plantaginaceae. For this reason, we’ve grouped the Orobanchaceae, Plantaginaceae, Phrymaceae and Scrophulariaceae together in this fle. In addition, species previously placed in the Callitrichaceae and Hippuridaceae families are now included in the Plantaginaceae family. 01a Plants aquatic, with many or all leaves submersed and limp when taken from the 1a water; leaves paired or in rings (whorled) on the stem, all or mostly linear (foating leaves sometimes spatula- to egg-shaped); fowers tiny (1-2 mm), single or clustered in leaf axils; petals and sepals absent or sepals fused in a cylinder around the ovary; stamens 0-1 . Plantaginaceae (in part) . - Callitriche, Hippuris 01b Plants emergent wetland species (with upper stems and leaves held above water) or upland species with self-supporting stems and leaves; leaves not as above; fowers larger, single or in clusters; petals and sepals present; stamens 2-4 (Hippuris sometimes emergent, but leaves/ fowers distinctive) . .02 2a 02a Plants without green leaves . Orobanchaceae (in part) . - Aphyllon [Orobanche], Boschniakia 02b Plants with green leaves . 03 03a Leaves all basal (sometimes small, unstalked stem leaves present), undivided (simple), with edges ± smooth or blunt-toothed; fowers small (2-5 mm wide), corollas radially symmetrical, sometimes absent. -
A Survey of Tricolpate (Eudicot) Phylogenetic Relationships1
American Journal of Botany 91(10): 1627±1644. 2004. A SURVEY OF TRICOLPATE (EUDICOT) PHYLOGENETIC RELATIONSHIPS1 WALTER S. JUDD2,4 AND RICHARD G. OLMSTEAD3 2Department of Botany, University of Florida, Gainesville, Florida 32611 USA; and 3Department of Biology, University of Washington, Seattle, Washington 98195 USA The phylogenetic structure of the tricolpate clade (or eudicots) is presented through a survey of their major subclades, each of which is brie¯y characterized. The tricolpate clade was ®rst recognized in 1989 and has received extensive phylogenetic study. Its major subclades, recognized at ordinal and familial ranks, are now apparent. Ordinal and many other suprafamilial clades are brie¯y diag- nosed, i.e., the putative phenotypic synapomorphies for each major clade of tricolpates are listed, and the support for the monophyly of each clade is assessed, mainly through citation of the pertinent molecular phylogenetic literature. The classi®cation of the Angiosperm Phylogeny Group (APG II) expresses the current state of our knowledge of phylogenetic relationships among tricolpates, and many of the major tricolpate clades can be diagnosed morphologically. Key words: angiosperms; eudicots; tricolpates. Angiosperms traditionally have been divided into two pri- 1992a; Chase et al., 1993; Doyle et al., 1994; Soltis et al., mary groups based on the presence of a single cotyledon 1997, 2000, 2003; KaÈllersjoÈ et al., 1998; Nandi et al., 1998; (monocotyledons, monocots) or two cotyledons (dicotyledons, Hoot et al., 1999; Savolainen et al., 2000a, b; Hilu et al., 2003; dicots). A series of additional diagnostic traits made this di- Zanis et al., 2003; Kim et al., 2004). This clade was ®rst called vision useful and has accounted for the long recognition of the tricolpates (Donoghue and Doyle, 1989), but the name these groups in ¯owering plant classi®cations. -
Tropical Aquatic Plants: Morphoanatomical Adaptations - Edna Scremin-Dias
TROPICAL BIOLOGY AND CONSERVATION MANAGEMENT – Vol. I - Tropical Aquatic Plants: Morphoanatomical Adaptations - Edna Scremin-Dias TROPICAL AQUATIC PLANTS: MORPHOANATOMICAL ADAPTATIONS Edna Scremin-Dias Botany Laboratory, Biology Department, Federal University of Mato Grosso do Sul, Brazil Keywords: Wetland plants, aquatic macrophytes, life forms, submerged plants, emergent plants, amphibian plants, aquatic plant anatomy, aquatic plant morphology, Pantanal. Contents 1. Introduction and definition 2. Origin, distribution and diversity of aquatic plants 3. Life forms of aquatic plants 3.1. Submerged Plants 3.2 Floating Plants 3.3 Emergent Plants 3.4 Amphibian Plants 4. Morphological and anatomical adaptations 5. Organs structure – Morphology and anatomy 5.1. Submerged Leaves: Structure and Adaptations 5.2. Floating Leaves: Structure and Adaptations 5.3. Emergent Leaves: Structure and Adaptations 5.4. Aeriferous Chambers: Characteristics and Function 5.5. Stem: Morphology and Anatomy 5.6. Root: Morphology and Anatomy 6. Economic importance 7. Importance to preserve wetland and wetlands plants Glossary Bibliography Biographical Sketch Summary UNESCO – EOLSS Tropical ecosystems have a high diversity of environments, many of them with high seasonal influence. Tropical regions are richer in quantity and diversity of wetlands. Aquatic plants SAMPLEare widely distributed in theseCHAPTERS areas, represented by rivers, lakes, swamps, coastal lagoons, and others. These environments also occur in non tropical regions, but aquatic plant species diversity is lower than tropical regions. Colonization of bodies of water and wetland areas by aquatic plants was only possible due to the acquisition of certain evolutionary characteristics that enable them to live and reproduce in water. Aquatic plants have several habits, known as life forms that vary from emergent, floating-leaves, submerged free, submerged fixed, amphibian and epiphyte. -
Phylogenie Der Farn- Und Blütenpflanzen Deutschlands
Schriftenreihe für Vegetationskunde H. 38 2002 75–91 Bundesamt für Naturschutz, Bonn Phylogenie der Farn- und Blütenpflanzen Deutschlands WALTER DURKA Summary: Phylogeny of the ferns and flowering plants of Germany A comprehensive phylogeny for the fern and flowering plant flora of Germany is presented representing the relationships among species and as a data basis for comparative analyses using phylogenetic independent contrasts. A supertree was constructed by assembling partial phylogenies mostly based on molecular DNA sequence data from more than 200 published sources. From these sources, the most parsimonious trees were used. The tree was construc- ted by manually pruning distal clades on basal clades. From the base to the family level, the tree is fully based on molecular studies. For intrafamilial relationships were no molecular stu- dies are available, classical systematic taxa (subfamilies, genera, subgenera etc.) were used as if representing phylogenies. The resolution of the tree, i.e the percentage of dichotomies is 66 % based upon 3212 taxa (without Rubus Sect. Rubus, Ranunculus auricomus agg. and with only 57 Hieracium spp.). Using only 50 % randomly chosen taxa (n = 1606) the reso- lution increases to 76 %. At the familial level the tree is totally resolved in angiosperms and gymnosperms whereas there are some polytomies in the ferns. At the generic level, there are 88 polytomies (e.g.: Poaceae: 17; Caryophyllaceae: 12; Lamiaceae: 8; Apiaceae: 7; Brassi- caceae: 7). Most polytomies are located at the species level (n = 993). A phylogenetic code as used in the program CAIC is given to each species in which at any node within the tree the branches are labelled A, B, C,… and for each taxon all labels are summed up. -
Pdf> (Accessed May 15, 2017)
TATIANA LOBATO-DE MAGALHÃES AND MAHINDA MARTÍNEZ* Botanical Sciences 96 (1): 138-156, 2018 Abstract Background: Mexico has a high diversity of aquatic and subaquatic plants that occur between 1,000 and 2,500 m of elevation, although a larger proportion of aquatic plants is concentrated at lower altitudes. Temporary wet- DOI: 10.17129/botsci.1532 lands harbor close to 73 % of the aquatic species in Mexico. These systems are under a strong anthropogenic pressure and suffer constant degradation. Received: Questions: i) How many species grow in highland temporary wetlands? ii) Are they floristically similar? iii) Is May 19th, 2017 there a latitudinal pattern of species richness? Accepted: Studied groups: Charophyta, Pteridophyta, Angiosperms. October 16th, 2017 Study site and years of study: Central Mexico (39 wetlands) from 2015 to 2016. Associated Editor: Methods: We collected in 39 temporary wetlands for two years. We made a presence/absence list of species per Martha Martínez Godillo locality, and calculated floristic similarities and correlations between wetlands. We include data characterizing life form, plant use, and conservation status. Results: We found 126 species belonging to 80 genera and 38 families. The richest families were Cyperaceae, Asteraceae, and Poaceae. As to genera, Eleocharis, Cyperus, and Juncus had more species. Species with the widest distributions were Persicaria mexicana, Marsilea mollis, Luziola fluitans, Heteranthera peduncularis, and Nymphoides fallax. We found five different life forms – all herbaceous, including 27 threatened species, 24 species with economic use, 48 endemic species, and 19 cosmopolitan species. In addition, we found 20 species recorded for the first time in some states included in our study, and two species ofEleocharis that might represent undescribed species.