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Natural Heritage Program List of Rare Plant Species of North Carolina 2016
Natural Heritage Program List of Rare Plant Species of North Carolina 2016 Revised February 24, 2017 Compiled by Laura Gadd Robinson, Botanist John T. Finnegan, Information Systems Manager North Carolina Natural Heritage Program N.C. Department of Natural and Cultural Resources Raleigh, NC 27699-1651 www.ncnhp.org C ur Alleghany rit Ashe Northampton Gates C uc Surry am k Stokes P d Rockingham Caswell Person Vance Warren a e P s n Hertford e qu Chowan r Granville q ot ui a Mountains Watauga Halifax m nk an Wilkes Yadkin s Mitchell Avery Forsyth Orange Guilford Franklin Bertie Alamance Durham Nash Yancey Alexander Madison Caldwell Davie Edgecombe Washington Tyrrell Iredell Martin Dare Burke Davidson Wake McDowell Randolph Chatham Wilson Buncombe Catawba Rowan Beaufort Haywood Pitt Swain Hyde Lee Lincoln Greene Rutherford Johnston Graham Henderson Jackson Cabarrus Montgomery Harnett Cleveland Wayne Polk Gaston Stanly Cherokee Macon Transylvania Lenoir Mecklenburg Moore Clay Pamlico Hoke Union d Cumberland Jones Anson on Sampson hm Duplin ic Craven Piedmont R nd tla Onslow Carteret co S Robeson Bladen Pender Sandhills Columbus New Hanover Tidewater Coastal Plain Brunswick THE COUNTIES AND PHYSIOGRAPHIC PROVINCES OF NORTH CAROLINA Natural Heritage Program List of Rare Plant Species of North Carolina 2016 Compiled by Laura Gadd Robinson, Botanist John T. Finnegan, Information Systems Manager North Carolina Natural Heritage Program N.C. Department of Natural and Cultural Resources Raleigh, NC 27699-1651 www.ncnhp.org This list is dynamic and is revised frequently as new data become available. New species are added to the list, and others are dropped from the list as appropriate. -
RI Equisetopsida and Lycopodiopsida.Indd
IIntroductionntroduction byby FFrancisrancis UnderwoodUnderwood Rhode Island Equisetopsida, Lycopodiopsida and Isoetopsida Special Th anks to the following for giving permission for the use their images. Robbin Moran New York Botanical Garden George Yatskievych and Ann Larson Missouri Botanical Garden Jan De Laet, plantsystematics.org Th is pdf is a companion publication to Rhode Island Equisetopsida, Lycopodiopsida & Isoetopsida at among-ri-wildfl owers.org Th e Elfi n Press 2016 Introduction Formerly known as fern allies, Horsetails, Club-mosses, Fir-mosses, Spike-mosses and Quillworts are plants that have an alternate generation life-cycle similar to ferns, having both sporophyte and gametophyte stages. Equisetopsida Horsetails date from the Devonian period (416 to 359 million years ago) in earth’s history where they were trees up to 110 feet in height and helped to form the coal deposits of the Carboniferous period. Only one genus has survived to modern times (Equisetum). Horsetails Horsetails (Equisetum) have jointed stems with whorls of thin narrow leaves. In the sporophyte stage, they have a sterile and fertile form. Th ey produce only one type of spore. While the gametophytes produced from the spores appear to be plentiful, the successful reproduction of the sporophyte form is low with most Horsetails reproducing vegetatively. Lycopodiopsida Lycopodiopsida includes the clubmosses (Dendrolycopodium, Diphasiastrum, Lycopodiella, Lycopodium , Spinulum) and Fir-mosses (Huperzia) Clubmosses Clubmosses are evergreen plants that produce only microspores that develop into a gametophyte capable of producing both sperm and egg cells. Club-mosses can produce the spores either in leaf axils or at the top of their stems. Th e spore capsules form in a cone-like structures (strobili) at the top of the plants. -
"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. -
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. -
Scientific Name Species Common Name Abies Lasiocarpa FIR Subalpine Acacia Macracantha ACACIA Long-Spine
Scientific Name Species Common Name Abies lasiocarpa FIR Subalpine Acacia macracantha ACACIA Long-spine Acacia roemeriana CATCLAW Roemer Acer grandidentatum MAPLE Canyon Acer nigrum MAPLE Black Acer platanoides MAPLE Norway Acer saccharinum MAPLE Silver Aesculus pavia BUCKEYE Red Aesculus sylvatica BUCKEYE Painted Ailanthus altissima AILANTHUS Tree-of-heaven Albizia julibrissin SILKTREE Mimosa Albizia lebbek LEBBEK Lebbek Alnus iridis ssp. sinuata ALDER Sitka Alnus maritima ALDER Seaside Alvaradoa amorphoides ALVARADOA Mexican Amelanchier laevis SERVICEBERRY Allegheny Amyris balsamifera TORCHWOOD Balsam Annona squamosa SUGAR-APPLE NA Araucaria cunninghamii ARAUCARIA Cunningham Arctostaphylos glauca MANZANITA Bigberry Asimina obovata PAWPAW Bigflower Bourreria radula STRONGBACK Rough Brasiliopuntia brasiliensis PRICKLY-PEAR Brazilian Bursera simaruba GUMBO-LIMBO NA Caesalpinia pulcherrima FLOWERFENCE NA Capparis flexuosa CAPERTREE Limber CRUCIFIXION- Castela emoryi THORN NA Casuarina equisetifolia CASUARINA Horsetail Ceanothus arboreus CEANOTHUS Feltleaf Ceanothus spinosus CEANOTHUS Greenbark Celtis lindheimeri HACKBERRY Lindheimer Celtis occidentalis HACKBERRY Common Cephalanthus occidentalis BUTTONBUSH Common Cercis canadensis REDBUD Eastern Cercocarpus traskiae CERCOCARPUS Catalina Chrysophyllum oliviforme SATINLEAF NA Citharexylum berlandieri FIDDLEWOOD Berlandier Citrus aurantifolia LIME NA Citrus sinensis ORANGE Orange Coccoloba uvifera SEAGRAPE NA Colubrina arborescens COLUBRINA Coffee Colubrina cubensis COLUBRINA Cuba Condalia globosa -
Group B: Grasses & Grass-Like Plants
Mangrove Guidebook for Southeast Asia Part 2: DESCRIPTIONS – Grasses & grass like plants GROUP B: GRASSES & GRASS-LIKE PLANTS 271 Mangrove Guidebook for Southeast Asia Part 2: DESCRIPTIONS – Grasses & grass like plants Fig. 25. Cyperus compactus Retz. (a) Habit, (b) spikelet, (c) flower and (d) nut. 272 Mangrove Guidebook for Southeast Asia Part 2: DESCRIPTIONS – Grasses & grass like plants CYPERACEAE 25 Cyperus compactus Retz. Synonyms : Cyperus dilutus Vahl., Cyperus grabowskianus Bolck., Cyperus luzonensis Llanos, Cyperus septatus Steud., Duraljouvea diluta Palla, Mariscus compactus Boldingh, Mariscus dilutus Nees, Mariscus microcephalus Presl., Sphaeromariscus microcephalus Camus Vernacular name(s) : Prumpungan, Jekeng, Suket (Ind.), Wampi lang (PNG), Baki-baking- pula, Durugi, Giron (Phil.). Description : A robust, perennial herb, 15-120 cm tall. Does not have stolons, and the rhizome is either very short or absent altogether. Stems are bluntly 3-angular, sometimes almost round, smooth, and with a diameter of up to 6 mm. The stem, leaves and sheath have numerous air-chambers. Leaves are 5-12 mm wide, stiff, deeply channelled, and as long as or shorter than the stem. Leaf edges and midrib are coarse towards the end of the leaf. Lower leaves are spongy and reddish-brown. Flowers are terminal and grouped in a large, up to 30 cm diameter umbrella-shaped cluster that has a reddish-brown colour. Large leaflets at the base of the flower cluster are up to 100 cm long. Spikelets (see illustration) are stemless and measure 5-15 by 1-1.5 mm. Ecology : Occurs in a variety of wetlands, including swamps, wet grasslands, coastal marshes, ditches, riverbanks, and occasionally in the landward margin of mangroves. -
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. -
Notes on Some Species of Diphasiastrum
Preslia, Praha, 47: 232 - 240, 1975 Notes on some species of Diphasiastrum Poznamky k n~kterym druhum rodu Dipha11iaatrum Josef Holub HOLUB J. (1975): Notes on some species of Diphasiastrum. - Preslia, Praha, 47: 232- 240. Taxonomic and nomenclatural problems of some species of Diphasiastrum HOLUB are discussed. A special attention is pa.id to the interspecies D. / X / issleri and D. / x / zei leri. Original plants of D. / x / issleri correspond to the combination D. alpinum - D. complanatum. Plants corresponding to the combination D. alpinum - D. tristachyum have been collected in the ~umava Mts. Some taxa described from the subarctic regions of Europe and North America are shown to belong most probably to the neglected interspecies D. / x / zeileri. Botanical I nstitute, Czechoslovak Academy of Sciences, 25~ 43 Prithonice, Czecho.,lovakia. INTRODUCTION This is a second part of my study of the new genus Diphasiastrum (HOLUB 1975), which could not be published in this journal in its entirety. Notes on taxonomy and nomenclature are selected from materials gathered originally for my "Catalogue of Czechoslovak vascular plants". With regard to the character of that work the present observations summarize the results of my own studies and suggests problems to be studied in the future. OBSERVATIONS f!.iphasiastrum alpinum (L.) HOLUB Two varieties have been described in this species (both under the name Lycopodium alpi nttm L.): var. thellungii HERTER from Switzerland and var. planiramulosum TAKEDA from Japan. Both these taxa, especially the first one, require a taxonomic revision; the possibility cannot be exclu<led that they are conspecific with D. / x / issleri. -
Protect Your Horses and Livestock from Toxic Plants
Protect Your Horses and Livestock From Toxic Plants A guide to identifying and controlling common, toxic noxious weeds and other toxic plant species. Protect your horses and livestock from toxic plants: A guide to identifying toxic noxious weeds and other toxic plant species Written by Genyce Hanson, with Alison Halpern, Wendy DesCamp, and Kittanya Locken; further reviewing by Tim Miller, Jennifer Andreas, Tricia MacLaren, Anna Lyon, Joan Mason and Casey Gozart. Layout by Kittanya Locken, with Becca Sotelo. Noxious weed classification in Washington: Class A: are nonnative, invasive plants whose distribution in Washington is still limited. Eradication of all Class A plants is required by law. Class B: are nonnative, invasive plants whose distribution is limited in some regions of Washington State, but widespread in others. Class B noxious weeds are designated for mandatory control in regions where they are still limited or absent. Class C: meet the criteria of noxious weeds but control is not required by the State Weed Board; county weed boards may require control of Class C noxious weeds if they are a local concern. Please check with your county weed board to learn more about the noxious weed control requirements where you live. WSDA Quarantine List: The Washington State Department of Agriculture (WSDA) maintains a quarantine list of plants whose sale or distribution is prohibited in Washington State. On the front cover: A palomino mare grazes in a safe, well-managed pasture with her foal. Photo credit: Sue Bird. On the back cover: Dairy cows enjoy a view of Rainier in a healthy, weed-free pasture. -
Pattern of Callose Deposition During the Course of Meiotic Diplospory in Chondrilla Juncea (Asteraceae, Cichorioideae)
Protoplasma DOI 10.1007/s00709-016-1039-y ORIGINAL ARTICLE Pattern of callose deposition during the course of meiotic diplospory in Chondrilla juncea (Asteraceae, Cichorioideae) Krystyna Musiał1 & Maria Kościńska-Pająk1 Received: 21 September 2016 /Accepted: 26 October 2016 # The Author(s) 2016. This article is published with open access at Springerlink.com Abstract Total absence of callose in the ovules of dip- Keywords Apomixis . Callose . Megasporogenesis . Ovule . losporous species has been previously suggested. This paper Chondrilla . Rush skeletonweed is the first description of callose events in the ovules of Chondrilla juncea, which exhibits meiotic diplospory of the Taraxacum type. We found the presence of callose in the Introduction megasporocyte wall and stated that the pattern of callose de- position is dynamically changing during megasporogenesis. Callose, a β-1,3-linked homopolymer of glucose containing At the premeiotic stage, no callose was observed in the ovules. some β-1,6 branches, may be considered as a histological Callose appeared at the micropylar pole of the cell entering marker for a preliminary identification of the reproduction prophase of the first meioticdivision restitution but did not mode in angiosperms. In the majority of sexually reproducing surround the megasporocyte. After the formation of a restitu- flowering plants, the isolation of the spore mother cell and the tion nucleus, a conspicuous callose micropylar cap and dis- tetrad by callose walls is a striking feature of both micro- and persed deposits of callose were detected in the megasporocyte megasporogenesis (Rodkiewicz 1970; Bhandari 1984; Bouman wall. During the formation of a diplodyad, the micropylar 1984; Lersten 2004). -
DANDELION Taraxacum Officinale ERADICATE
OAK OPENINGS REGION BEST MANAGEMENT PRACTICES DANDELION Taraxacum officinale ERADICATE This Best Management Practice (BMP) document provides guidance for managing Dandelion in the Oak Openings Region of Northwest Ohio and Southeast Michigan. This BMP was developed by the Green Ribbon Initiative and its partners and uses available research and local experience to recommend environmentally safe control practices. INTRODUCTION AND IMPACTS— Dandelion (Taraxacum officinale) HABITAT—Dandelion prefers full sun and moist, loamy soil but can is native to Eurasia and was likely introduced to North America many grow anywhere with 3.5-110” inches of annual precipitation, an an- times. The earliest record of Dandelion in North America comes from nual mean temperature of 40-80°F, and light. It is tolerant of salt, 1672, but it may have arrived earlier. It has been used in medicine, pollutants, thin soils, and high elevations. In the OOR Dandelion has food and beverages, and stock feed. Dandelion is now widespread been found on sand dunes, in and at the top of floodplains, near across the planet, including OH and MI. vernal pools and ponds, and along roads, ditches, and streams. While the Midwest Invasive Species Information Net- IDENTIFICATION—Habit: Perennial herb. work (MISIN) has no specific reports of Dandelion in or within 5 miles of the Oak Openings Region (OOR, green line), the USDA Plants Database reports Dan- D A delion in all 7 counties of the OOR and most neighboring counties (black stripes). Dan- delion is ubiquitous in the OOR. It has demonstrated the ability to establish and MI spread in healthy and disturbed habitats of OH T © Lynn Sosnoskie © Steven Baskauf © Chris Evans the OOR and both the wet nutrient rich soils of wet prairies and floodplains as well Leaves: Highly variable in shape, color and hairiness in response to as sandy dunes and oak savannas. -
An Evaluation of the Wetland and Upland Habitats And
AN EVALUATION OF THE WETLAND AND UPLAND HABITATS AND ASSOCIATED WILDLIFE RESOURCES IN SOUTHERN CANAAN VALLEY CANAAN VALLEY TASK FORCE SUBMl'l*IED BY: EDWIN D. MICHAEL, PH.D. PROFESSOR OF WILDLIFEMANAGEI\fENT DIVISION OF FORESTRY WEST VIRGINIA UNIVERSITY MORGANTOWN, WV 26506 December 1993 TABLB OP' CONTENTS Page EXECUTIVE SUMMARY 1 INTRODUCTION 6 OBJECTIVES 6 PROCEDURES 6 THE STUDY AREA Canaan Valley .... ..... 7 Southern Canaan Valley .... 8 Development and Land Use 8 Existing Environment Hydrology ........ 9 Plant Communities .... 11 1. Northern hardwoods . 11 2. Conifers ... 11 3. Aspen groves . 11 4. Alder thickets 12 5. Ecotone 12 6. Shrub savannah 12 7. Spiraea 13 8. Krummholz 13 9. Bogs ..... 13 10. Beaver ponds 13 11. Agriculture . l4 Vegetation of Southern Canaan Valley Wetlands 14 Rare and Endangered Plant Species 16 Vertebrate Animals 16 1. Fishes .. 16 2. Amphibians 18 3. Reptiles 19 4. Birds 20 5. Mammals 24 Rare and Endangered Animal Species 25 Game Animals 27 Cultural Values 28 Aesthetic Values 31 1. Landform contrast 31 2. Land-use contrast 31 3. Wetland-type diversity 32 4. Internal wetland contrast 32 5. Wetland size ... 32 6. Landform diversity .... 32 DISCUSSION Streams 32 Springs and Spring Seeps 34 Lakes . 35 Wetland Habitats 35 ii Wildlife 36 Management Potential 38 Off-road Vehicle Use 42 Fragmentation . 42 Cultural Values 44 Educational Values SIGNIFICANCE OF THE AREA OF CONCERN FOR FULFILLMENT OF THE CANAAN VALLEY NATIONAL WILDLIFE REFUGE 1979 EIS OBJECTIVES 46 CONCLUSIONS .. 47 LITERATURE CITED 52 TABLES 54 FIGURES 88 iii LIST OF TABLES 1. Property ownerships of Canaan Valley ... ..... 8 2.