Connecticut Invasive Plant List January 2004
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Verticillium Wilt of Fraxinus Excelsior
Verticillium wilt of Fraxinus excelsior - ' . ; Jt ""* f- "" UB-^/^'IJ::J CENTRALE LANDBOUWCATALOGUS 0000 0611 8323 locjs Promotoren: Dr.Ir. R.A.A. Oldeman Hoogleraar ind e Bosteelt en Bosoecologie Dr.Ir. J. Dekker Emeritus Hoogleraar ind e Fytopathologie /OMOS-Zöl,^ Jelle A. Hiemstra Verticillium wilt of Fraxinus excelsior Proefschrift ter verkrijging van de graad van doctor in de landbouw- en milieuwetenschappen, op gezag van de rector magnificus, dr. C.M. Karssen, inhe t openbaar te verdedigen op dinsdag 18apri l 1995 des namiddags omvie r uur ind e aula van de Landbouwuniversiteit te Wageningen J\ ABSTRACT Hiemstra, J.A. (1995). Verticillium wilt of Fraxinus excelsior. PhD Thesis, Wageningen Agricultural University, The Netherlands, xvi + 213 pp, 40 figs., 28 tables, 4 plates with colour pictures, 327 refs., English and Dutch summaries. ISBN 90-5485-360-3 Research on ash wilt disease, a common disease of Fraxinus excelsior L. in young forest and landscape plantings in several parts of the Netherlands, is described. By means of a survey for pathogenic fungi in affected trees, inoculation and reisolation experimentsi ti sdemonstrate d thatth ediseas ei scause db y Verticilliumdahliae Kleb . Hostspecificit y andvirulenc e of aV. dahliae isolatefro m ashar ecompare d tothos e of isolatesfro m elm,mapl ean dpotato .Diseas eincidenc ean dprogress , andrecover y of infected trees are investigated through monitoring experiments in two permanent plots in seriously affected forest stands. Monitoring results are related to the results of an aerial survey for ash wilt disease in the province of Flevoland to assess the impact of the disease on ash forests. -
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 -
Status and Strategy for Flowering Rush (Butomus Umbellatus L.) Management
State of Michigan’s Status and Strategy for Flowering Rush (Butomus umbellatus L.) Management Scope Invasive flowering rush (Butomus umbellatus L., hereafter FR) has invaded the shores of Michigan waterways since the early 1900’s (Core 1941; Stuckey 1968; Anderson et al. 1974). This document was developed by Central Michigan University and reviewed by Michigan Departments of Environmental Quality and Natural Resources for the purposes of: • Summarizing the current level of understanding on the biology and ecology of FR. • Summarizing current management options for FR in Michigan. • Identifying possible future directions of FR management in Michigan. This document used the current information available in journals, publications, presentations, and experiences of leading researchers and managers to meet its goals. Any chemical, company, or organization that is mentioned was included for its involvement in published, presented, or publically shared information, not to imply endorsement of the chemical, company, or organization. Biology and Ecology I. Identification Flowering rush is an emergent aquatic perennial plant with linear, sword-like leaves, triangular in cross-section, and a showy umble of pink flowers (Figure 1). Rhizomes (i.e. horizonal root-like stems) are fleshy, and leaves have parallel veination and can be submersed or emergent. Submersed leaves are linear and limp, unlike sword-like emergent leaves. Flowering rush blooms from June to August. Flowers are arranged in terminal umbels. Flower parts are found in multiples of three (e.g. six tepals, nine stamen, six carpels) with pink to purple tepals 0.25 – 0.5 in (6 - 11.5 mm) long (eFloras 2008). Each flower produces up to six beaked fruits. -
Columbia Basin Flowering Rush Management Plan
COLUMBIA BASIN COOPERATIVE WEED MANAGEMENT AREA COLUMBIA BASIN FLOWERING RUSH MANAGEMENT PLAN A regional strategy to address Butomus umbellatus throughout the Columbia Basin www.columbiabasincwma.org Statement of Collaboration: When possible, the partners of the Columbia Basin Cooperative Weed Management Area will strive to communicate and work collaboratively to develop a unified management effort for flowering rush throughout the Columbia Basin. The completion of this document was supported by funding from the National Fish and Wildlife Foundation Suggested citation: Columbia Basin Cooperative Weed Management Area. 2019. Columbia Basin Flowering Rush Management Plan: A regional strategy to address Butomus umbellatus throughout the Columbia Basin. pp 67 www.columbiabasincwma.org Pg. 1 CONTENT Tables ....................................................................................................................................... 3 Figures ..................................................................................................................................... 3 Preface ..................................................................................................................................... 5 Executive Summary .................................................................................................................. 6 Introduction ............................................................................................................................. 7 Scope and Purpose ........................................................................................................................7 -
CHINESE PRIVET Due to Its Ability to Successfully Compete with And
Plant Guide by this species is large-scale ecosystem modification CHINESE PRIVET due to its ability to successfully compete with and Ligustrum sinense Lour. displace native vegetation. Chinese privet plants Plant Symbol = LISI mature rapidly and are prolific seed producers. They also reproduce vegetatively by means of root suckers. Contributed by: USDA NRCS National Plant Data Once established, Chinese privet is difficult to Center & Louisiana State University-Plant Science; eradicate because of its reproductive capacity. partial funding from the US Geological Survey and the US National Biological Information Impact/Vectors: Ligustrum sinense is native to China Infrastructure and was introduced into the United States in 1852 for use as an ornamental shrub. It is used for hedge and mass plantings, and sometimes as single specimens for its foliage and its profusion of small white flowers (Dirr 1990; Wyman 1973). It continues to be widely sold in the nursery and gardening industry. The foliage of Chinese privet is also used, presumably, for cut-flower arrangements. This horticultural introduction has been cultivated for a relatively long time in the United States. Wyman (1973) reports that this species is still growing as a hedge on the old Berkman’s Nursery grounds in Augusta, Georgia, where it was planted in the early 1860’s. It was planted on the Chickamauga and Chattanooga National Military Park after it came under the control of the Secretary of War in 1890. Present day plants are descendants of those early plantings (Faulkner et al. 1989). According to Small (1933), the species was escaping from cultivation in southern Louisiana by the 1930’s. -
Taxonomic Overview of Ligustrum (Oleaceae) Naturalizaed in North America North of Mexico
Phytologia (December 2009) 91(3) 467 TAXONOMIC OVERVIEW OF LIGUSTRUM (OLEACEAE) NATURALIZAED IN NORTH AMERICA NORTH OF MEXICO Guy L. Nesom 2925 Hartwood Drive Fort Worth, TX 76109, USA www.guynesom.com ABSTRACT A key, morphological descriptions, and basic synonymy are provided for the eight species of Ligustrum known to be naturalized in North America north of Mexico: L. japonicum, L. lucidum, L. obtusifolium (including L. amurense), L. ovalifolium, L. quihoui, L. sinense, L. tschonoskii, and L. vulgare. Identifications have been inconsistent particularly between L. sinense and L. vulgare and between L. japonicum and L. lucidum. The occurrence of L. quihoui outside of cultivation in Arkansas, Mississippi, and Oklahoma is documented. Phytologia 91(3): 467-482 (December, 2009). KEY WORDS: Ligustrum, Oleaceae, North America, naturalized, taxonomy The lustrous, mostly evergreen leaves and masses of white, fragrant flowers make privets popular for landscaping and hedges. Many of the species, however, have become naturalized in the USA and Canada and already have proved to be destructive colonizers, especially in the Southeast. Among the naturalized species, European privet (Ligustrum vulgare) is native to Europe and northern Africa; all the rest are native to Asia, mainly China, Japan, and Korea. Many new species and varieties of Ligustrum have been described since overviews of Koehne (1904), Lingelsheim (1920), and Mansfield (1924). The genus in eastern Asia has recently been studied by Chang & Miao (1986), and Qin (2009) has provided a taxonomic overview of the whole genus that recognizes 37 species - divided into five sections based primarily on fruit and seed morphology. In Qin’s arrangement, among the North American species, sect. -
Ecology and Phenology of Flowering Rush in the Detroit Lakes Chain of Lakes, Minnesota
J. Aquat. Plant Manage. 53: 54–63 Ecology and phenology of flowering rush in the Detroit Lakes chain of lakes, Minnesota MICHELLE D. MARKO, JOHN D. MADSEN, R. A. SMITH, B. SARTAIN, AND C. L. OLSON* ABSTRACT al. 1974, Boutwell 1990, Brown and Eckert 2005). Flowering rush can form monotypic stands that crowd out native Flowering rush, Butomus umbellatus L., has been an plants and interfere with recreational water use and water increasing problem in the Detroit Lakes chain of lakes for flow (Boutwell 1990, Jacobs et al. 2011). In the St. Lawrence more than 40 yr. Flowering rush dominates ecosystems by River region, it was found to be more invasive than purple crowding out native species, including hardstem bulrush, loosestrife (Lythrum salicaria L.; Lavoie 2003). The spread of Schoenoplectus acutus (Muhl. ex Bigelow) A & D Love,¨ a vital flowering rush in irrigation ditches has affected water flow part of native ecosystems. Furthermore, flowering rush and become a management concern for native fish species, creates boating hazards and hampers recreational activities such as cutthroat and bull trout (Jacobs et al. 2011). One on the lakes. The phenological differences between flower- region in Minnesota, the Pelican River Watershed, has been ing rush and the native hardstem bulrush were examined as struggling with flowering rush for over 40 yr as it has spread part of a project to determine best management practices through the Detroit Lakes chain of lakes since the 1960s (T. for controlling this invasive species. Biomass allocation, Guetter, Pelican River Watershed District, pers. comm.). plant height, carbohydrate allocation, and reproductive Since its introduction as an ornamental species in Lake structures of flowering rush were examined in the Detroit Sallie (Becker County, Minnesota), different methods of Lakes system. -
EUROPEAN PRIVET [Ligustrum Vulare L.] LIVU
EUROPEAN PRIVET [Ligustrum vulare L.] LIVU Fig. 1 UGA 5369085 Problem: Native to Europe, L. vulgare. was brought to North America as an ornamental in the 1700’s.1 It escaped cultivation and displaces native species by forming dense thickets.2 Habit: Stout, multi-stem trunk growing up to 4.5 m tall with unevenly spreading branches.3 Often as wide as tall.4 Stems and leaves at near right angles.5 Reproduction: Sexually by seeds from drupes which are widely disseminated by birds.4 Leaves: Simple, opposite, ovate to elliptic, margins entire. Lustrous green above and pale green beneath, turning purple in the fall. 2.5-7 cm long.2, 4 Fig. 2 UGA 5272067 SHRUBPLANT EUROPEAN PRIVET Ligustrum vulgare L. Fig. 3 UGA 5397688 Fruits/Seeds: Lustrous4 dark purple to black, spherical, about 8.5mm long drupe.3 Flowers: Arranged in a terminal 2.5-7.5 cm panicle.2 Individual flowers small (2.5-3 mm)6 are tubular with four lobes that are equal or less than the length of the tube. Sta- mens are mostly included or slightly projecting from tube.6 Flowers are white, with a strong scent.2 Habitat: Full sun or partial shade.4 Often found in areas of disturbed soil, along streams, and in the forest understory (though it does not produce seed in low light).1, 3 Similar Species: Ligustrum species are difficult to distin- guish vegetatively. L. obtusifolium has a flower tube about twice as long its the lobesGC and its leaves are smaller, blunt-tipped, and have a pubescent mid-rib.7 Fig. -
Identification and Control of Invasive Privets (Ligustrum Spp.) in the Middle Southern United States
Invasive Plant Science and Management 2010 3:482–488 Notes and Commentary Identification and Control of Invasive Privets (Ligustrum spp.) in the Middle Southern United States Victor Maddox, John Byrd, Jr., and Brett Serviss* The identification of privet in the middle southern United States can be difficult. Because most introduced species of privet can be invasive, and recent mapping projects seek location and species population data, proper identification is important. Without proper identification of privet species, data on species distributions and other pertinent information regarding invasiveness could lead to improper conclusions. Currently, information on privet identification is scattered throughout a number of reference materials. The purpose of this publication is to assist with the proper identification of escaped privet species, and suggest management options. Nomenclature: Fosamine ammonium; glyphosate; hexazinone; imazapyr; metsulfuron; triclopyr; 2,4-D; 2,4-DP; Amur privet, Ligustrum obtusifolium Sieb. & Zucc. var. suave (Kitagawa) Kitagawa (Syn. L. amurense Carrie`re); border privet, Ligustrum obtusifolium Sieb. & Zucc. var. obtusifolium; California privet, Ligustrum ovalifolium Hassk.; Chinese privet, Ligustrum sinense Lour.; common privet, Ligustrum vulgare L.; glossy privet, Ligustrum lucidum Ait.; Japanese privet, Ligustrum japonicum Thunb.; waxyleaf privet, Ligustrum quihoui Carrie`re. Key words: Invasive species, management. Since the 1700s, at least nine species of privets have been Thunb.) is native to Korea and Japan. The most common introduced into the United States; it is probable that all species in the southern portion of the middle southern were introduced as ornamentals. They have been very region is Chinese privet, although Amu, border, California, successful as ornamentals and continue to be marketed for common or European, glossy, Japanese, and waxyleaf or such purposes. -
Ligustrum Sinense LOUR.)
CAUSES AND CONSEQUENCES OF CHINESE PRIVET (Ligustrum sinense LOUR.) INVASION IN HYDROLOGICALLY ALTERED FORESTED WETLANDS Meghan Foard A thesis presented to the faculty of Arkansas State University in partial fulfillment of the requirements of the degree of MASTER OF SCIENCE IN ENVIRONMENTAL SCIENCE Arkansas State University August 2014 Approved by Dr. Travis D. Marsico, Thesis Advisor Dr. Jennifer Bouldin Committee Member Dr. Richard Grippo, Committee Member Dr. Esra Ozdenerol, Committee Member Dr. Paul Sikkel, Committee Member UMI Number: 1563273 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a complete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. UMI 1563273 Published by ProQuest LLC (2014). Copyright in the Dissertation held by the Author. Microform Edition © ProQuest LLC. All rights reserved. This work is protected against unauthorized copying under Title 17, United States Code ProQuest LLC. 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, MI 48106 - 1346 © 2014 Meghan Foard ALL RIGHTS RESERVED ii ABSTRACT Meghan Foard CAUSES AND CONSEQUENCES OF CHINESE PRIVET (Ligustrum sinense LOUR.) INVASION IN HYDROLOGICALLY ALTERED FORESTED WETLANDS What drives invasive species success? My research consists of four studies aiming to answer this question for Ligustrum sinense. The four projects are: (1) Synthesis of invasion literature within passenger-driver-backseat driver frameworks; (2) hydrochory investigation of water as a dispersal mechanism for invasion; (3) ecohydrology investigation of inundation effects on seed viability of L. -
Flowering Rush
IPANE - Catalog of Species Search Results http://www.lib.uconn.edu/webapps/ipane/browsing.cfm?descriptionid=16 Home | Early Detection | IPANE Species | Data & Maps | Volunteers | About the Project | Related Information Catalog of Species Search Results Butomus umbellatus (Flowering rush ) :: Catalog of Species Search Common Name(s) | Full Scientific Name | Family Name Common | Family Scientific Name | Images | Synonyms | Description | Similar Species | Reproductive/Dispersal Mechanisms | Distribution | History of Introduction in New England | Habitats in New England | Threats | Early Warning Notes | Management Links | Documentation Needs | Additional Information | References | Data Retrieval | Maps of New England Plant Distribution COMMON NAME Flowering rush FULL SCIENTIFIC NAME Butomus umbellatus L. FAMILY NAME COMMON Flowering rush family FAMILY SCIENTIFIC NAME Butomaceae IMAGES Flowers Habit Flowers Fruit Incursion Roots 1 of 5 9/24/2007 3:36 PM IPANE - Catalog of Species Search Results http://www.lib.uconn.edu/webapps/ipane/browsing.cfm?descriptionid=16 Habitat NOMENCLATURE/SYNONYMS Synonyms: Butomus umbellatus f. vallisneriifolius (Sagorski) Gluck DESCRIPTION Botanical Glossary Butomus umbellatus is a perennial, aquatic herb that grows from a fleshy rhizome on freshwater shorelines. It can be found in water several meters deep, and its flowering stem can reach up to 1 m (3.3 ft.) above the surface of the water. The 0.6-0.9 m (2-3 ft.) long ensiform leaves can be erect or floating on the water's surface. The leaves are three angled, fleshy and have twisted ends. The plants flower from the summer to the fall depending on the depth of the water. The flowers are arranged in a bracted umbel. The bracts are purple-tinged, and numerous flowers are on long, slender ascending pedicels. -
Species-Related Variability of Hydrological Properties of The
Species‐related variability of hydrological properties of the branches of 12 deciduous tree species Klamerus‐Iwan Anna1*, Łagan Sylwia2 Zarek Marcin3, Słowik‐Opoka Ewa1, Bartłomiej Wojtan1 Supplementary Materials a) b) c) Syringa vulgaris L upper surface: a) water, b) diiodomethane, c) glycerin a) b) c) Syringa vulgaris L lower surface: a) water, b) diiodomethane, c) glycerin a) b) c) Betula pendula upper surface a) water, b) diiodomethane, c) glycerin a) b) c) Betula pendula lower surface a) water, b) diiodomethane, c) glycerin a) b) c) Quercus robur upper surface a) water, b) diiodomethane, c) glycerin a) b) c) Quercus robur lower surface a) water, b) diiodomethane, c) glycerin a) b) c) Fraxinus excelsior upper surface a) water, b) diiodomethane, c) glycerin a) b) c) Fraxinus excelsior lower surface a) water, b) diiodomethane, c) glycerin a) b) c) Aesculus hippocastanum upper surface a) water, b) diiodomethane, c) glycerin a) b) c) Aesculus hippocastanum upper surface a) water, b) diiodomethane, c) glycerin a) b) c) Acer platanoides upper surface a) water, b) diiodomethane, c) glycerin a) b) c) Acer platanoides lower surface a) water, b) diiodomethane, c) glycerin a) b) c) Ligustrum vulgare upper surface a) water, b) diiodomethane, c) glycerin a) b) c) Ligustrum vulgare upper surface a) water, b) diiodomethane, c) glycerin a) b) c) Tilia cordata upper surface a) water, b) diiodomethane, c) glycerin a) b) c) Tilia cordata lower surface a) water, b) diiodomethane, c) glycerin a) b) c) Elaeagnus angustifolia upper surface a) water, b) diiodomethane,