Vascular Flora of Worcester, Massachusetts

Total Page:16

File Type:pdf, Size:1020Kb

Vascular Flora of Worcester, Massachusetts Vascular Flora of Worcester, Massachusetts Robert I. Bertin Special Publication of the New England Botanical Club Availability of this Publication: Electronic or paper copies are available at cost. Direct inquiries to the Special Publications Committee, New England Botanical Club, Harvard University Herbaria, 22 Divinity Ave. Cambridge, MA 02138-2020 About the Author: Robert I. Bertin is a professor of biology in the Biology Department at the College of the Holy Cross. He teaches a variety of courses, including ecology, environmental biology and field botany. His academic interests include the flora and natural history of New England, the sexual systems of flowering plants, and the ecology of invasive species. Additions and Corrections: Communications concerning mistakes in this flora or potential additions to the species list are welcome. Any substantive modifications will be posted under the author’s name on the Biology Department web page at the Holy Cross web site. The author can be contacted through the Biology Department or at [email protected]. Cover Illustrations: Pictured are three species portraying different aspects of the Worcester flora. Acer platanoides, or Norway maple, is a non-native species and the most commonly planted street tree in Worcester. It is prominent in many City woodlands, where it competes with native species. The grass Elymus villosus is a state threatened species. The Worcester record is the only known occurrence of the species in Worcester County. The orchid Calopogon tuberosus, a native bog species, is known in the City only from historical records. Figures reprinted from Holmgren et al. (1998) Illustrated Companion to Gleason and Cronquist’s Manual, with the kind permission of the New York Botanical Garden. Vascular Flora of Worcester, Massachusetts Robert I. Bertin Biology Department College of the Holy Cross Worcester, Massachusetts 01610 Copyright © 2000 Robert I. Bertin All rights reserved Special Publication of the New England Botanical Club Table of Contents Acknowledgments ................................................................................................................. 1 Preface ................................................................................................................................... 1 Introduction ........................................................................................................................... 2 The Physical Setting .............................................................................................................. 2 Geology ................................................................................................................................. 5 Climate .................................................................................................................................. 6 Soils ....................................................................................................................................... 7 The Human Impact ................................................................................................................ 8 Vegetation ............................................................................................................................ 12 Methodology ........................................................................................................................ 15 Explanation of the Species List ........................................................................................... 15 Species Summary ................................................................................................................ 18 Species List: Ferns and Fern Allies ..................................................................................... 21 Species List: Gymnosperms ................................................................................................ 25 Species List: Dicotyledons .................................................................................................. 26 Species List: Monocotyledons ........................................................................................... 106 Appendix I – Sampling Sites ............................................................................................. 134 Appendix II – Fugitives and Waifs ................................................................................... 137 Appendix III – Species Excluded ...................................................................................... 139 Literature Cited .................................................................................................................. 140 Index .................................................................................................................................. 142 List of Tables and Figures Figure 1. Map of Worcester, Massachusetts showing locations of sampling sites and major roads ................................................................................................................ 3 Figure 2. Map of Worcester, Massachusetts showing topography and locations of streams and ponds ...................................................................................................... 4 Table 1. Percentage of Worcester occupied by forest, wetland and water at different times ........................................................................................................................ 10 Table 2. Taxonomic summary of the Worcester flora ........................................................ 18 Table 3. New Worcester County records ........................................................................... 19 1 Acknowledgments I thank the many individuals who have assisted me in this work. David Boufford, C. Barre Hellquist, Thomas Philbrick, Tom Rawinski, Karen Searcy, Paul Somers and Lisa Standley helped with difficult identifications. Tom Rawinski generously shared his knowledge of the flora of central Massachusetts and contributed several species records. Les Mehrhoff of the University of Connecticut herbarium, Ray Angelo, Maureen Kerwin, Tim Whitfield and Emily Wood of the Harvard University Herbaria, Stan Herwitz of the Hadwen Herbarium at Clark University, Karen Searcy of the University of Massachusetts Herbarium, Aaron Ellison of Mount Holyoke College, and Anthony Kirchgessner of the New York Botanical Garden provided information on specimens or assistance in the use of their respective facilities. Edmund Schofield helped track down historical information. Arthur Allen, Jennifer Bravo, George Hoffmann and Karen Searcy kindly reviewed a draft of the manuscript. Anne Barry, Susan Hunt, Lorrie Parent, Ken Scott and Joel Villa assisted with computer software. Hugo Cárdenas kindly made available the GIS facilities of Worcester’s Office of Planning and Community Development where Erin Whitaker expertly drafted the two maps. Special thanks to the NEBC special publication committee, Karen Searcy, Paul Somers and Lisa Standley, for their advice and careful editing of the manuscript. Holy Cross College and the Marshall Fund supported various aspects of this work. Finally, numerous landowners permitted access to their properties in the City, without which this work would not have been possible. Preface The southern New England states, including Massachusetts, probably contain a greater density of practicing botanists than any other state or province in the Western Hemisphere. Despite this fact, the botanical landscape is poorly known. New native vascular plant species continue to be added to state totals. The work for this flora in one city uncovered over 80 plant species that had not previously been recorded anywhere in the county. No complete flora of Massachusetts has ever been published (though parts were treated by Ahmadjian 1979), and no generally accepted classification of plant communities of this state has yet been developed. Thus, we have much to learn about our green environment. Floras for single towns or cities are uncommon. The only Massachusetts town floras from the past half century are Blake’s The Flora of Stoughton, Massachusetts (1964), Eaton’s A Flora of Concord (1974), and Sorrie and Dunwiddie’s The Vascular and Non-Vascular Flora of Nantucket, Tuckernut, and Muskeget Islands (1996). One might argue that the considerable effort required to produce a flora is of limited value when the geographic coverage is so restricted, and that one’s efforts are more profitably directed to a county, state, or region. Several regional floras cover the Worcester area, including Fernald (1950), Seymour (1972), Gleason and Cronquist (1991), Flora of North America Committee (1993-2000) and Magee and Ahles (1999). While floras at these larger scales are immensely valuable, they are necessarily limited in specificity. From a regional flora, for example, it can be difficult to determine the actual frequency with which a species occurs. By working at a more local level, it is possible to give much more detailed information on frequency, abundance, and distribution, and therefore on changes over time and the impact of human activities, as has been observed by Whitney (1994). 2 A floristic survey of an urban area is also somewhat unusual in that botanists tend to focus on more natural environments. A notable exception is the massive New York Metropolitan Flora project now underway under the auspices of the Brooklyn Botanic Garden. Such surveys of urban areas are helpful in allowing documentation of the loss of native species and the
Recommended publications
  • Field Release of the Leaf-Feeding Moth, Hypena Opulenta (Christoph)
    United States Department of Field release of the leaf-feeding Agriculture moth, Hypena opulenta Marketing and Regulatory (Christoph) (Lepidoptera: Programs Noctuidae), for classical Animal and Plant Health Inspection biological control of swallow- Service worts, Vincetoxicum nigrum (L.) Moench and V. rossicum (Kleopow) Barbarich (Gentianales: Apocynaceae), in the contiguous United States. Final Environmental Assessment, August 2017 Field release of the leaf-feeding moth, Hypena opulenta (Christoph) (Lepidoptera: Noctuidae), for classical biological control of swallow-worts, Vincetoxicum nigrum (L.) Moench and V. rossicum (Kleopow) Barbarich (Gentianales: Apocynaceae), in the contiguous United States. Final Environmental Assessment, August 2017 Agency Contact: Colin D. Stewart, Assistant Director Pests, Pathogens, and Biocontrol Permits Plant Protection and Quarantine Animal and Plant Health Inspection Service U.S. Department of Agriculture 4700 River Rd., Unit 133 Riverdale, MD 20737 Non-Discrimination Policy The U.S. Department of Agriculture (USDA) prohibits discrimination against its customers, employees, and applicants for employment on the bases of race, color, national origin, age, disability, sex, gender identity, religion, reprisal, and where applicable, political beliefs, marital status, familial or parental status, sexual orientation, or all or part of an individual's income is derived from any public assistance program, or protected genetic information in employment or in any program or activity conducted or funded by the Department. (Not all prohibited bases will apply to all programs and/or employment activities.) To File an Employment Complaint If you wish to file an employment complaint, you must contact your agency's EEO Counselor (PDF) within 45 days of the date of the alleged discriminatory act, event, or in the case of a personnel action.
    [Show full text]
  • "National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary."
    Intro 1996 National List of Vascular Plant Species That Occur in Wetlands The Fish and Wildlife Service has prepared a National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary (1996 National List). The 1996 National List is a draft revision of the National List of Plant Species That Occur in Wetlands: 1988 National Summary (Reed 1988) (1988 National List). The 1996 National List is provided to encourage additional public review and comments on the draft regional wetland indicator assignments. The 1996 National List reflects a significant amount of new information that has become available since 1988 on the wetland affinity of vascular plants. This new information has resulted from the extensive use of the 1988 National List in the field by individuals involved in wetland and other resource inventories, wetland identification and delineation, and wetland research. Interim Regional Interagency Review Panel (Regional Panel) changes in indicator status as well as additions and deletions to the 1988 National List were documented in Regional supplements. The National List was originally developed as an appendix to the Classification of Wetlands and Deepwater Habitats of the United States (Cowardin et al.1979) to aid in the consistent application of this classification system for wetlands in the field.. The 1996 National List also was developed to aid in determining the presence of hydrophytic vegetation in the Clean Water Act Section 404 wetland regulatory program and in the implementation of the swampbuster provisions of the Food Security Act. While not required by law or regulation, the Fish and Wildlife Service is making the 1996 National List available for review and comment.
    [Show full text]
  • Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE
    Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE LILIACEAE de Jussieu 1789 (Lily Family) (also see AGAVACEAE, ALLIACEAE, ALSTROEMERIACEAE, AMARYLLIDACEAE, ASPARAGACEAE, COLCHICACEAE, HEMEROCALLIDACEAE, HOSTACEAE, HYACINTHACEAE, HYPOXIDACEAE, MELANTHIACEAE, NARTHECIACEAE, RUSCACEAE, SMILACACEAE, THEMIDACEAE, TOFIELDIACEAE) As here interpreted narrowly, the Liliaceae constitutes about 11 genera and 550 species, of the Northern Hemisphere. There has been much recent investigation and re-interpretation of evidence regarding the upper-level taxonomy of the Liliales, with strong suggestions that the broad Liliaceae recognized by Cronquist (1981) is artificial and polyphyletic. Cronquist (1993) himself concurs, at least to a degree: "we still await a comprehensive reorganization of the lilies into several families more comparable to other recognized families of angiosperms." Dahlgren & Clifford (1982) and Dahlgren, Clifford, & Yeo (1985) synthesized an early phase in the modern revolution of monocot taxonomy. Since then, additional research, especially molecular (Duvall et al. 1993, Chase et al. 1993, Bogler & Simpson 1995, and many others), has strongly validated the general lines (and many details) of Dahlgren's arrangement. The most recent synthesis (Kubitzki 1998a) is followed as the basis for familial and generic taxonomy of the lilies and their relatives (see summary below). References: Angiosperm Phylogeny Group (1998, 2003); Tamura in Kubitzki (1998a). Our “liliaceous” genera (members of orders placed in the Lilianae) are therefore divided as shown below, largely following Kubitzki (1998a) and some more recent molecular analyses. ALISMATALES TOFIELDIACEAE: Pleea, Tofieldia. LILIALES ALSTROEMERIACEAE: Alstroemeria COLCHICACEAE: Colchicum, Uvularia. LILIACEAE: Clintonia, Erythronium, Lilium, Medeola, Prosartes, Streptopus, Tricyrtis, Tulipa. MELANTHIACEAE: Amianthium, Anticlea, Chamaelirium, Helonias, Melanthium, Schoenocaulon, Stenanthium, Veratrum, Toxicoscordion, Trillium, Xerophyllum, Zigadenus.
    [Show full text]
  • 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,
    [Show full text]
  • 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
    [Show full text]
  • 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
    [Show full text]
  • Rubiaceae), and the Description of the New Species Galianthe Vasquezii from Peru and Colombia
    Morphological and molecular data confirm the transfer of homostylous species in the typically distylous genus Galianthe (Rubiaceae), and the description of the new species Galianthe vasquezii from Peru and Colombia Javier Elias Florentín1, Andrea Alejandra Cabaña Fader1, Roberto Manuel Salas1, Steven Janssens2, Steven Dessein2 and Elsa Leonor Cabral1 1 Herbarium CTES, Instituto de Botánica del Nordeste, Corrientes, Argentina 2 Plant systematic, Botanic Garden Meise, Meise, Belgium ABSTRACT Galianthe (Rubiaceae) is a neotropical genus comprising 50 species divided into two subgenera, Galianthe subgen. Galianthe, with 39 species and Galianthe subgen. Ebelia, with 11 species. The diagnostic features of the genus are: usually erect habit with xylopodium, distylous flowers arranged in lax thyrsoid inflorescences, bifid stigmas, 2-carpellate and longitudinally dehiscent fruits, with dehiscent valves or indehiscent mericarps, plump seeds or complanate with a wing-like strophiole, and pollen with double reticulum, rarely with a simple reticulum. This study focused on two species that were originally described under Diodia due to the occurrence of fruits indehiscent mericarps: Diodia palustris and D. spicata. In the present study, classical taxonomy is combined with molecular analyses. As a result, we propose that both Diodia species belong to Galianthe subgen. Ebelia. The molecular position within Galianthe, based on ITS and ETS sequences, has been supported by the following morphological Submitted 10 June 2017 characters: thyrsoid, spiciform or cymoidal inflorescences, bifid stigmas, pollen grains Accepted 19 October 2017 with a double reticulum, and indehiscent mericarps. However, both species, unlike the Published 23 November 2017 remainder of the genus Galianthe, have homostylous flowers, so the presence of this Corresponding author type of flower significantly modifies the generic concept.
    [Show full text]
  • State of New York City's Plants 2018
    STATE OF NEW YORK CITY’S PLANTS 2018 Daniel Atha & Brian Boom © 2018 The New York Botanical Garden All rights reserved ISBN 978-0-89327-955-4 Center for Conservation Strategy The New York Botanical Garden 2900 Southern Boulevard Bronx, NY 10458 All photos NYBG staff Citation: Atha, D. and B. Boom. 2018. State of New York City’s Plants 2018. Center for Conservation Strategy. The New York Botanical Garden, Bronx, NY. 132 pp. STATE OF NEW YORK CITY’S PLANTS 2018 4 EXECUTIVE SUMMARY 6 INTRODUCTION 10 DOCUMENTING THE CITY’S PLANTS 10 The Flora of New York City 11 Rare Species 14 Focus on Specific Area 16 Botanical Spectacle: Summer Snow 18 CITIZEN SCIENCE 20 THREATS TO THE CITY’S PLANTS 24 NEW YORK STATE PROHIBITED AND REGULATED INVASIVE SPECIES FOUND IN NEW YORK CITY 26 LOOKING AHEAD 27 CONTRIBUTORS AND ACKNOWLEGMENTS 30 LITERATURE CITED 31 APPENDIX Checklist of the Spontaneous Vascular Plants of New York City 32 Ferns and Fern Allies 35 Gymnosperms 36 Nymphaeales and Magnoliids 37 Monocots 67 Dicots 3 EXECUTIVE SUMMARY This report, State of New York City’s Plants 2018, is the first rankings of rare, threatened, endangered, and extinct species of what is envisioned by the Center for Conservation Strategy known from New York City, and based on this compilation of The New York Botanical Garden as annual updates thirteen percent of the City’s flora is imperiled or extinct in New summarizing the status of the spontaneous plant species of the York City. five boroughs of New York City. This year’s report deals with the City’s vascular plants (ferns and fern allies, gymnosperms, We have begun the process of assessing conservation status and flowering plants), but in the future it is planned to phase in at the local level for all species.
    [Show full text]
  • Environmental Niche Partitioning Among Riparian Sedges {Carex, Cyperaceae) in the St. Lawrence Valley, Quebec
    Environmental niche partitioning among riparian sedges {Carex, Cyperaceae) in the St. Lawrence Valley, Quebec Laura Plourde Master of Science Department of Biology McGill University Montreal, Quebec, Canada A thesis submitted to the Faculty of Graduate Studies and Research in partial fulfillment of requirements of the degree of Master of Science August 31st, 2007 ©Copyright Laura Plourde 2007. All rights reserved. Library and Bibliotheque et 1*1 Archives Canada Archives Canada Published Heritage Direction du Branch Patrimoine de I'edition 395 Wellington Street 395, rue Wellington Ottawa ON K1A0N4 Ottawa ON K1A0N4 Canada Canada Your file Votre reference ISBN: 978-0-494-51322-4 Our file Notre reference ISBN: 978-0-494-51322-4 NOTICE: AVIS: The author has granted a non­ L'auteur a accorde une licence non exclusive exclusive license allowing Library permettant a la Bibliotheque et Archives and Archives Canada to reproduce, Canada de reproduire, publier, archiver, publish, archive, preserve, conserve, sauvegarder, conserver, transmettre au public communicate to the public by par telecommunication ou par Plntemet, prefer, telecommunication or on the Internet, distribuer et vendre des theses partout dans loan, distribute and sell theses le monde, a des fins commerciales ou autres, worldwide, for commercial or non­ sur support microforme, papier, electronique commercial purposes, in microform, et/ou autres formats. paper, electronic and/or any other formats. The author retains copyright L'auteur conserve la propriete du droit d'auteur ownership and moral rights in et des droits moraux qui protege cette these. this thesis. Neither the thesis Ni la these ni des extraits substantiels de nor substantial extracts from it celle-ci ne doivent etre imprimes ou autrement may be printed or otherwise reproduits sans son autorisation.
    [Show full text]
  • Etude Sur L'origine Et L'évolution Des Variations Florales Chez Delphinium L. (Ranunculaceae) À Travers La Morphologie, L'anatomie Et La Tératologie
    Etude sur l'origine et l'évolution des variations florales chez Delphinium L. (Ranunculaceae) à travers la morphologie, l'anatomie et la tératologie : 2019SACLS126 : NNT Thèse de doctorat de l'Université Paris-Saclay préparée à l'Université Paris-Sud ED n°567 : Sciences du végétal : du gène à l'écosystème (SDV) Spécialité de doctorat : Biologie Thèse présentée et soutenue à Paris, le 29/05/2019, par Felipe Espinosa Moreno Composition du Jury : Bernard Riera Chargé de Recherche, CNRS (MECADEV) Rapporteur Julien Bachelier Professeur, Freie Universität Berlin (DCPS) Rapporteur Catherine Damerval Directrice de Recherche, CNRS (Génétique Quantitative et Evolution Le Moulon) Présidente Dario De Franceschi Maître de Conférences, Muséum national d'Histoire naturelle (CR2P) Examinateur Sophie Nadot Professeure, Université Paris-Sud (ESE) Directrice de thèse Florian Jabbour Maître de conférences, Muséum national d'Histoire naturelle (ISYEB) Invité Etude sur l'origine et l'évolution des variations florales chez Delphinium L. (Ranunculaceae) à travers la morphologie, l'anatomie et la tératologie Remerciements Ce manuscrit présente le travail de doctorat que j'ai réalisé entre les années 2016 et 2019 au sein de l'Ecole doctorale Sciences du végétale: du gène à l'écosystème, à l'Université Paris-Saclay Paris-Sud et au Muséum national d'Histoire naturelle de Paris. Même si sa réalisation a impliqué un investissement personnel énorme, celui-ci a eu tout son sens uniquement et grâce à l'encadrement, le soutien et l'accompagnement de nombreuses personnes que je remercie de la façon la plus sincère. Je remercie très spécialement Florian Jabbour et Sophie Nadot, mes directeurs de thèse.
    [Show full text]
  • Pinery Provincial Park Vascular Plant List Flowering Latin Name Common Name Community Date
    Pinery Provincial Park Vascular Plant List Flowering Latin Name Common Name Community Date EQUISETACEAE HORSETAIL FAMILY Equisetum arvense L. Field Horsetail FF Equisetum fluviatile L. Water Horsetail LRB Equisetum hyemale L. ssp. affine (Engelm.) Stone Common Scouring-rush BS Equisetum laevigatum A. Braun Smooth Scouring-rush WM Equisetum variegatum Scheich. ex Fried. ssp. Small Horsetail LRB Variegatum DENNSTAEDIACEAE BRACKEN FAMILY Pteridium aquilinum (L.) Kuhn Bracken-Fern COF DRYOPTERIDACEAE TRUE FERN FAMILILY Athyrium filix-femina (L.) Roth ssp. angustum (Willd.) Northeastern Lady Fern FF Clausen Cystopteris bulbifera (L.) Bernh. Bulblet Fern FF Dryopteris carthusiana (Villars) H.P. Fuchs Spinulose Woodfern FF Matteuccia struthiopteris (L.) Tod. Ostrich Fern FF Onoclea sensibilis L. Sensitive Fern FF Polystichum acrostichoides (Michaux) Schott Christmas Fern FF ADDER’S-TONGUE- OPHIOGLOSSACEAE FERN FAMILY Botrychium virginianum (L.) Sw. Rattlesnake Fern FF FLOWERING FERN OSMUNDACEAE FAMILY Osmunda regalis L. Royal Fern WM POLYPODIACEAE POLYPODY FAMILY Polypodium virginianum L. Rock Polypody FF MAIDENHAIR FERN PTERIDACEAE FAMILY Adiantum pedatum L. ssp. pedatum Northern Maidenhair Fern FF THELYPTERIDACEAE MARSH FERN FAMILY Thelypteris palustris (Salisb.) Schott Marsh Fern WM LYCOPODIACEAE CLUB MOSS FAMILY Lycopodium lucidulum Michaux Shining Clubmoss OF Lycopodium tristachyum Pursh Ground-cedar COF SELAGINELLACEAE SPIKEMOSS FAMILY Selaginella apoda (L.) Fern. Spikemoss LRB CUPRESSACEAE CYPRESS FAMILY Juniperus communis L. Common Juniper Jun-E DS Juniperus virginiana L. Red Cedar Jun-E SD Thuja occidentalis L. White Cedar LRB PINACEAE PINE FAMILY Larix laricina (Duroi) K. Koch Tamarack Jun LRB Pinus banksiana Lambert Jack Pine COF Pinus resinosa Sol. ex Aiton Red Pine Jun-M CF Pinery Provincial Park Vascular Plant List 1 Pinery Provincial Park Vascular Plant List Flowering Latin Name Common Name Community Date Pinus strobus L.
    [Show full text]
  • Flora and Fauna Guarantee Act 1988 Protected Flora List November 2019
    Department of Environment, Land, Water & Planning Flora and Fauna Guarantee Act 1988 Protected Flora List November 2019 What is Protected Flora? Protected flora are native plants or communities of native plants that have legal protection under the Flora and Fauna Guarantee Act 1988. The Protected Flora List includes plants from three sources: plant taxa (species, subspecies or varieties) listed as threatened under the Flora and Fauna Guarantee Act 1988 plant taxa belonging to communities listed as threatened under the Flora and Fauna Guarantee Act 1988 plant taxa which are not threatened but require protection for other reasons. For example, some species which are attractive or highly sought after, such as orchids and grass trees, are protected so that the removal of these species from the wild can be controlled. For all listed species protection includes living (eg flowers, seeds, shoots and roots) and non-living (eg bark, leaves and other litter) plant material. Do I need a permit or licence? The handling of protected flora is regulated by the Department of Environment, Land, Water & Planning (DELWP) to ensure that any harvesting or loss is ecologically sustainable. You must obtain a ‘Protected Flora Licence’ or Permit from one of the Regional Offices of DELWP if you want to collect protected native plants or if you are planning to do works or other activities on public land which might kill, injure or disturb protected native plants. In most cases, you do not require a Licence or Permit for works or activities on private land, although you may require a planning permit from your local council.
    [Show full text]