Pocket Field Guide Ngr - Slender Naiad - Najas Gracillima 2
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Red Names=Invasive Species Green Names=Native Species
CURLY-LEAF PONDWEED EURASIAN WATERMIL- FANWORT CHARA (Potamogeton crispus) FOIL (Cabomba caroliniana) (Chara spp.) This undesirable exotic, also known (Myriophyllum spicatum) This submerged exotic Chara is typically found growing in species is not common as Crisp Pondweed, bears a waxy An aggressive plant, this exotic clear, hard water. Lacking true but management tools are cuticle on its upper leaves making milfoil can grow nearly 10 feet stems and leaves, Chara is actually a limited. Very similar to them stiff and somewhat brittle. in length forming dense mats form of algae. It’s stems are hollow aquarium species. Leaves The leaves have been described as at the waters surface. Grow- with leaf-like structures in a whorled are divided into fine resembling lasagna noodles, but ing in muck, sand, or rock, it pattern. It may be found growing branches in a fan-like ap- upon close inspection a row of has become a nuisance plant with tiny, orange fruiting bodies on pearance, opposite struc- “teeth” can be seen to line the mar- in many lakes and ponds by the branches called akinetes. Thick ture, spanning 2 inches. gins. Growing in dense mats near quickly outcompeting native masses of Chara can form in some Floating leaves are small, the water’s surface, it outcompetes species. Identifying features areas. Often confused with Starry diamond shape with a native plants for sun and space very include a pattern of 4 leaves stonewort, Coontail or Milfoils, it emergent white/pinkish early in spring. By midsummer, whorled around a hollow can be identified by a gritty texture flower. -
Biodegradable Benthic Mats As an Alternative to Conventional IAP Control
Going to the Mat: Biodegradable benthic mats for invasive aquatic plant control ©The Nature Conservancy/Big Foot Media Andrew Tucker & Lindsay Chadderton (The Nature Conservancy) Anna K. Monfils, Blake Cahill, & Heather Dame (Central Michigan Univ) Pam Tyning & Paul Hausler (Progressive A/E) Ryan Thum (Montana State Univ) James McNair (Grand Valley State Univ) Conventional control options • Chemical • Mechanical • Biological • Physical www.blackoaklake.com (including shade/ smothering) Lance Wynn, The Grand Rapids Press Traditional barriers Traditional bottom barriers Lakemat.com Biodegradable benthic mats Caffrey et al. 2010 Aquatic Invasions 5: 123-129 Biodegradable benthic mats JUTE MAT JUTE FIBER JUTE PLANT Biodegradable benthic mats Hofstra & Clayton 2012 J Aquat. Plant Manage. 50: MISGP Integrated aquatic plant pest management: Refining and expanding the management toolbox Objectives 1) Understand mechanisms for variable success of herbicide treatment for EWM 2) Assess efficacy of herbicide treatments for CFW and SSW 3) Assess efficacy of benthic barriers to control EWM, CFW and SSW Cabomba caroliniana ©The Nature Conservancy/Big Foot Media Cabomba caroliniana Discoverlife.org Sheldon Naive Cabomba caroliniana Cabomba caroliniana Cabomba caroliniana Invadingspecies.com Management options - Prevention - Chemical - Mechanical - Biological - Shading Schooler 2008. Shade as a management tool for Cabomba caroliniana. J. Aquat Plant Manage. 46: 168-171. Barton Lake (Kalamazoo Co., MI) Preliminary Rake Toss Survey 10m x 10m plots (benthic -
Hydrilla Vs. New York
1 comicvine.com Hydrilla vs. New York UMISC October 16, 2018 2 Hydrilla in New York High priority species prohibited by Part 575 Now found at 32 locations throughout New York Often found near boat launches DeviantArt Waterfowl also considered a vector 3 Hydrilla in New York First discovered in 2008 2008 - Creamery Pond, Orange County 2008 – Sans Souci Lake, Lotus Lake, Suffolk County 2009 - Lake Ronkonkoma, Blydenburgh/New Mill Pond, Phillips Mill Pond, Suffolk County 2009 – Frost Mill Pond, Suffolk County 2011- Smith Pond, Great Patchoque Lake, Suffolk County; Cayuga Inlet, Tompkins County 2012 – several private ponds, Broome County 2012 – Cayuga Lake, Tompkins County; Tonawanda/Erie Canal, Niagara and Erie Counties 2013 – Croton River, Westchester County 2013 – Millers Pond, Suffolk County; Unnamed pond, Tioga County 2014 – New Croton Reservoir, Westchester County 2014 – Prospect Park, Brooklyn, Kings County 2015 – Tinker Nature Park pond, Monroe County 2016 – Aurora (Cayuga Lake), Tompkins County 2016 – Spencer Pond, Tioga County 2016 – Halsey Neck Road Pond, Suffolk County 2018 - Kuhlman Pond, Tioga County 2018 - Avon Pond, Frank Melville Pond, and East Setauket, Suffolk County 2018 – Allison Pond, Staten Island, Richmond County 4 Management Options in Place 1) No management 2) Benthic mats 3) Triploid Grass Carp 4) Herbicide 5) Combination (IPM) 5 Option: No management Suffolk County: • Lake Ronkonkoma (10 acres of 240 acres) • Sans Souci (southern 5 acres) • Lotus Lake (13 acres) • Blydenburgh/New Mill Pond (110 acres, coverage -
New York Non-Native Plant Invasiveness Ranking Form
NEW YORK NON -NATIVE PLANT INVASIVENESS RANKING FORM Scientific name: Callitriche stagnalis Scop. USDA Plants Code: CAST Common names: pond water-starwort Native distribution: Europe, Asia, North Africa Date assessed: July 1, 2008 Assessors: Steve Clemants Reviewers: LIISMA SRC Date Approved: July 9, 2008 Form version date: 10 July 2009 New York Invasiveness Rank: Low (Relative Maximum Score 40.00-49.99) Distribution and Invasiveness Rank (Obtain from PRISM invasiveness ranking form ) PRISM Status of this species in each PRISM: Current Distribution Invasiveness Rank 1 Adirondack Park Invasive Program Not Assessed Not Assessed 2 Capital/Mohawk Not Assessed Not Assessed 3 Catskill Regional Invasive Species Partnership Not Assessed Not Assessed 4 Finger Lakes Not Assessed Not Assessed 5 Long Island Invasive Species Management Area Restricted Insignificant 6 Lower Hudson Not Assessed Not Assessed 7 Saint Lawrence/Eastern Lake Ontario Not Assessed Not Assessed 8 Western New York Not Assessed Not Assessed Invasiveness Ranking Summary Total (Total Answered*) Total (see details under appropriate sub-section) Possible 1 Ecological impact 40 (30) 9 2 Biological characteristic and dispersal ability 25 (22 ) 12 3 Ecological amplitude and distribution 25 (25) 15 4 Difficulty of control 10 (3) 3 Outcome score 100 (80 )b 39a † Relative maximum score 48.75 § New York Invasiveness Rank Low (Relative Maximum Score 40.00-49.99) * For questions answered “unknown” do not include point value in “Total Answered Points Possible.” If “Total Answered Points Possible” is less than 70.00 points, then the overall invasive rank should be listed as “Unknown.” †Calculated as 100(a/b) to two decimal places. -
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 -
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. -
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 -
Aquatic Vascular Plant Species Distribution Maps
Appendix 11.5.1: Aquatic Vascular Plant Species Distribution Maps These distribution maps are for 116 aquatic vascular macrophyte species (Table 1). Aquatic designation follows habitat descriptions in Haines and Vining (1998), and includes submergent, floating and some emergent species. See Appendix 11.4 for list of species. Also included in Appendix 11.4 is the number of HUC-10 watersheds from which each taxon has been recorded, and the county-level distributions. Data are from nine sources, as compiled in the MABP database (plus a few additional records derived from ancilliary information contained in reports from two fisheries surveys in the Upper St. John basin organized by The Nature Conservancy). With the exception of the University of Maine herbarium records, most locations represent point samples (coordinates were provided in data sources or derived by MABP from site descriptions in data sources). The herbarium data are identified only to township. In the species distribution maps, town-level records are indicated by center-points (centroids). Figure 1 on this page shows as polygons the towns where taxon records are identified only at the town level. Data Sources: MABP ID MABP DataSet Name Provider 7 Rare taxa from MNAP lake plant surveys D. Cameron, MNAP 8 Lake plant surveys D. Cameron, MNAP 35 Acadia National Park plant survey C. Greene et al. 63 Lake plant surveys A. Dieffenbacher-Krall 71 Natural Heritage Database (rare plants) MNAP 91 University of Maine herbarium database C. Campbell 183 Natural Heritage Database (delisted species) MNAP 194 Rapid bioassessment surveys D. Cameron, MNAP 207 Invasive aquatic plant records MDEP Maps are in alphabetical order by species name. -
Elodea Genus: Egeria Or Elodea Family: Hydrocharitaceae Order: Hydrocharitales Class: Liliopsida Phylum: Magnoliophyta Kingdom: Plantae
Elodea Genus: Egeria or Elodea Family: Hydrocharitaceae Order: Hydrocharitales Class: Liliopsida Phylum: Magnoliophyta Kingdom: Plantae Conditions for Customer Ownership We hold permits allowing us to transport these organisms. To access permit conditions, click here. Never purchase living specimens without having a disposition strategy in place. The USDA does not require any special permits to ship and/or receive Elodea except in Puerto Rico, where shipment of aquatic plants is prohibited. However, in order to continue to protect our environment, you must house your Elodea in an aquarium. Under no circumstances should you release your Elodea into the wild. Primary Hazard Considerations Always wash your hands thoroughly before and after you handle your Elodea, or anything it has touched. Availability Elodea is available year round. Elodea should arrive with a green color, it should not be yellow or “slimy.” • Elodea canadensis—Usually bright green with three leaves that form whorls around the stem. The whorls compact as they get closer to the tip. Found completely submerged. Is generally a thinner species of Elodea. Has a degree of seasonality May–June. • Egeria densa—Usually bright green with small strap-shaped leaves with fine saw teeth. 3–6 leaves form whorls around the stem and compact as they get closer to the tip. Usually can grow to be a foot or two long. Is thicker and bushier than E. canadensis. Elodea arrives in a sealed plastic bag. Upon arrival, this should be opened and Elodea should be kept moist, or it should be placed in a habitat. For short term storage (1–2 weeks), Elodea should be placed in its bag into the refriger- ator (4 °C). -
Download the Full Report Pdf, 2.9 MB
VKM Report 2016:50 Assessment of the risks to Norwegian biodiversity from the import and keeping of aquarium and garden pond plants Opinion of the Panel on Alien Organisms and Trade in Endangered Species (CITES) of the Norwegian Scientific Committee for Food Safety Report from the Norwegian Scientific Committee for Food Safety (VKM) 2016:50 Assessment of the risks to Norwegian biodiversity from the import and keeping of aquarium and garden pond plants Opinion of the Panel on Alien Organisms and Trade in Endangered Species (CITES) of the Norwegian Scientific Committee for Food Safety 01.11.2016 ISBN: 00000-00000 Norwegian Scientific Committee for Food Safety (VKM) Po 4404 Nydalen N – 0403 Oslo Norway Phone: +47 21 62 28 00 Email: [email protected] www.vkm.no www.english.vkm.no Suggested citation: VKM (2016). Assessment of the risks to Norwegian biodiversity from the import and keeping of aquarium and garden pond plants. Scientific Opinion on the on Alien Organisms and Trade in Endangered species of the Norwegian Scientific Committee for Food Safety ISBN: 978-82-8259-240-6, Oslo, Norway. VKM Report 2016:50 Title: Assessment of the risks to Norwegian biodiversity from the import and keeping of aquarium and garden pond plants Authors preparing the draft opinion Hugo de Boer (chair), Maria G. Asmyhr (VKM staff), Hanne H. Grundt, Inga Kjersti Sjøtun, Hans K. Stenøien, Iris Stiers. Assessed and approved The opinion has been assessed and approved by Panel on Alien organisms and Trade in Endangered Species (CITES). Members of the panel are: Vigdis Vandvik (chair), Hugo de Boer, Jan Ove Gjershaug, Kjetil Hindar, Lawrence Kirkendall, Nina Elisabeth Nagy, Anders Nielsen, Eli K. -
Resolution of Deep Angiosperm Phylogeny Using Conserved Nuclear Genes and Estimates of Early Divergence Times
ARTICLE Received 24 Mar 2014 | Accepted 11 Aug 2014 | Published 24 Sep 2014 DOI: 10.1038/ncomms5956 OPEN Resolution of deep angiosperm phylogeny using conserved nuclear genes and estimates of early divergence times Liping Zeng1, Qiang Zhang2, Renran Sun1, Hongzhi Kong3, Ning Zhang1,4 & Hong Ma1,5 Angiosperms are the most successful plants and support human livelihood and ecosystems. Angiosperm phylogeny is the foundation of studies of gene function and phenotypic evolution, divergence time estimation and biogeography. The relationship of the five divergent groups of the Mesangiospermae (B99.95% of extant angiosperms) remains uncertain, with multiple hypotheses reported in the literature. Here transcriptome data sets are obtained from 26 species lacking sequenced genomes, representing each of the five groups: eudicots, monocots, magnoliids, Chloranthaceae and Ceratophyllaceae. Phylogenetic analyses using 59 carefully selected low-copy nuclear genes resulted in highly supported relationships: sisterhood of eudicots and a clade containing Chloranthaceae and Ceratophyllaceae, with magnoliids being the next sister group, followed by monocots. Our topology allows a re-examination of the evolutionary patterns of 110 morphological characters. The molecular clock estimates of Mesangiospermae diversification during the late to middle Jurassic correspond well to the origins of some insects, which may have been a factor facilitating early angiosperm radiation. 1 State Key Laboratory of Genetic Engineering and Collaborative Innovation Center for Genetics and Development, Ministry of Education Key Laboratoryof Biodiversity Sciences and Ecological Engineering, Institute of Plant Biology, Institute of Biodiversity Science, Center for Evolutionary Biology, School of Life Sciences, Fudan University, 220 Handan Road, Yangpu District, Shanghai 200433, China. 2 Guangxi Institute of Botany, Guangxi Zhuang Autonomous Region and the Chinese Academy of Sciences, Guilin 541006, China.